Efficient perovskite solar cells require metal halide perovskite (MHP) films of consistent and reproducible high quality. MHP films are frequently prepared through a solution-based solvent-engineering spin coating approach. This processing involves considering various controllable parameters (e.g. spin speed) and ones that are more difficult to control (e.g. changes in atmosphere) to fabricate MHP films reliably. To address this issue, we developed a closed-loop feedback system based on a multimodal optical in situ spectroscopy spin coater system. We combine this system with real-time monitoring and analysis of the optical spectra during the spin coating process. As soon as a parameter of interest reaches a predefined target level, perovskite crystallization is automatically induced by dispensing the antisolvent via a syringe pump. To demonstrate our approach, we optically monitor the precursor solution film thickness as the parameter of interest during the spin coating. We intentionally vary the evaporation kinetics by spin coating at different spin speeds between 2000 and 1250 rpm and compare our reactive method to the common time-based approach. We find that our method reliably counteracts effects like variation in solvent evaporation rate due to atmospheric changes and reduces the human impact on the processing, thus leading to reproducible film quality for all spin speeds without any optimization steps.

The Urbach energy as a measure of energetic disorder is an important characteristic of semiconductors to evaluate their optoelectronic functionality. However, discrepancies occur in Urbach energy values EU determined via different measurement and analysis methods, whose origin of a profound understanding is still missing. To reliably analyze the origin of such discrepancies, we recorded quasi-simultaneously temperature-dependent absorption and photoluminescence (PL) spectra of halide perovskite (MAPbI3) thin-film and single-crystal samples. Performing profound Urbach analyses in an extended energy range down to 0.2 eV below the bandgap, we find energy-range-dependent exaggeration effects on Urbach energy values to be only present in the near bandgap region (∼0.02 eV below the bandgap), where non-Urbach absorption states start to contribute. Besides that, generally lower EU values and a lower temperature-dependence of EU are obtained from PL than from absorption, which originates from the sensitivity of PL for sites with lower energetic disorder and/or higher phonon energies in the excited-state geometry. Thus, our work is sensitized to proper interpretation and comparison of EU values and contributes to developing a more fundamental understanding of semiconductor materials.

Optical pump–probe techniques allow for an in-depth study of dark excited states. Here, we utilize them to map and gain insights into the excited states involved in the thermally activated delayed fluorescence (TADF) mechanism of a benchmark TADF emitter DMAC-TRZ. The results identify different electronic excited states involved in the key TADF transitions and their nature by combining pump–probe and photoluminescence measurements. The photoinduced absorption signals are highly dependent on polarity, affecting the transition oscillator strength but not their relative energy positions. In methylcyclohexane, a strong and vibronically structured local triplet excited state absorption (3LE → 3LEn) is observed, which is quenched in higher polarity solvents as 3CT becomes the lowest triplet state. Furthermore, ultrafast transient absorption (fsTA) confirms the presence of two stable conformers of DMAC-TRZ: (1) quasi-axial (QA) interconverting within 20 ps into (2) quasi-equatorial (QE) in the excited state. Moreover, fsTA highlights how sensitive excited state couplings are to the environment and the molecular conformation.

It is generally believed that intrinsic charge generation via an autoionization mechanism in pristine single-component organic semiconductors is impossible upon photoexcitation within the lowest excited singlet state due to the large exciton binding energy. However, we present measurements of thermally stimulated luminescence, light-induced ESR, and photocurrent in the carbazole-based molecule 3′,5-di(9H-carbazol-9-yl)-[1,1′-biphenyl]-3-carbonitrile (mCBP-CN) films, revealing that charge-carrier pairs are efficiently produced upon excitation near their absorption edges. The photocurrent measurements show a superlinear dependence on the cw-photoexcitation intensity even at very low excitation power (below 1mW/cm2), suggesting a bimolecular nature of the charge photogeneration process. The photocurrent measured over a broad temperature range of 5–300 K exhibits a prominent maximum at moderately low temperature around 170 K and rolls off significantly at higher temperatures. This correlates remarkably with the maximum of delayed fluorescence induced by bimolecular triplet-triplet annihilation (TTA), i.e., triplet fusion, in this material. This behavior implies that the photocurrent is governed mainly by the TTA-induced production of geminate pairs and only a little by their subsequent dissociation. Moreover, we find that the field-assisted dissociation probability of photogenerated charge pairs becomes almost temperature-independent at temperatures below 100 K. This can be quantitatively described using a charge dissociation model accounting for the energy disorder and the distribution of geminate-pair radii. The key conclusion of this study is that triplet fusion can promote the energy up-conversion (to 5.42 eV), thereby enabling the autoionization of a high-energy neutral excited state. This serves as the predominant mechanism of intrinsic photogeneration in this single-component heavy-atom-free system. We attribute the effect to efficient intersystem crossing in mCBP-CN, a high triplet energy level (2.71 eV), and very long-lived triplet excitations. A broader implication of this finding is that the so far neglected mechanism of TTA-facilitated charge-carrier generation might be relevant for organic long-persistent luminescence materials, and even for organic photovoltaics and potentially for photocatalytic water splitting processes.

The optoelectronic performance of organic semiconductor devices is related to the static and dynamic disorder in the film. The disorder can be assessed by considering the linewidth of its optical spectra. We focus on identifying the effect of conjugation length distribution on the static energetic disorder. Hence, we disentangle the contributions of static and dynamic disorder to the absorption and emission spectra of poly(3-(2,5-dioctylphenyl)-thiophene) (PDOPT) by exploring how the linewidth and energy of the spectra evolve upon cooling the sample from 300 K to 5 K. PDOPT has sterically hindered side chains that arrange such as to cause a planarized polymer backbone. This makes it a suitable model for a quasi-one-dimensional molecular system. By modelling the conjugated segments as coupled oscillators we find that the linewidth contribution resulting from the variation of conjugation length decreases linearly with decreasing exciton energy and extrapolates to zero at the energy corresponding to an infinite chain. These results provide a new avenue to the design of low disorder and hence high mobility polymeric semiconductors.

Ionic liquids, such as BMIMBF4, are added to mixed halide perovskites to prevent halide phase segregation and increase phase stability, but exact mechanisms changing halide kinetics are currently unclear. Here, X-ray diffraction, nuclear magnetic resonance, and photoluminescence spectroscopy are used in situ under dark conditions to follow thermally driven halide mixing processes forming MAPbI3–xBrx from physical mixtures of MAPbI3 and MAPbBr3 powders with and without BMIMBF4. Halide migration is significantly accelerated with BMIMBF4 compared to additive-free mixtures. This is attributed to liquid-like dynamics of BMIMBF4 at elevated temperatures, liberating defect sites at perovskite interfaces. Furthermore, the presence of BMIMBF4 increases the activation energies for bromide migration, suggesting a changed nature of the latter. This is explained by a preferred interaction between BMIM+ and bromide, indicating that the cations of the additive shuttle bromide ions between interfaces. Overall, these observations pave the way for a better understanding of halide transport in hybrid perovskites.

Intramolecular through-space charge transfer thermally activated delayed fluorescence (TSCT-TADF) has attracted much attention recently as it can achieve both small energy splitting and high emission efficiency. However, the relationship of excited states between TSCT and through-bond charge transfer (TBCT) remains a challenge in the TSCT-TADF molecules. Herein, three compounds DPS-m-bAc, DPS-p-bAc, and DPS-OAc that possess emissive TSCT and/or TBCT states are prepared. Interestingly, a so-called inverted energy gap is found for both DPS-m-bAc and DPS-p-bAc in toluene solution, which results from the different charge transfer states of ICThigh and ICTlow, as proved by the detailed transient photoluminescence and calculated results. Intense emission from blue to yellow associated with high photoluminescence quantum yields of 70–100% are measured in doped polymethyl(methacrylate) (PMMA) films. Notably, compound DPS-m-bAc achieves the highest reverse intersystem crossing rate constant (kRISC) of over 107 s−1 in a PMMA film, benefiting from close-lying TSCT and TBCT states. The solution-processed device with DPS-m-bAc displays a maximum external quantum efficiency of 21.7% and a relatively small efficiency roll-off (EQE of 20.2% @ 100 cd m−2). Overall, this work demonstrates how with judicious emitter engineering, a synergy between different charge transfer excited states, can be achieved, providing an avenue to achieve highly efficient solution-processed OLEDs.

Modern organic semiconductors frequently adopt a semicrystalline morphology which makes the analysis of charge transport challenging. In this paper, we employ Monte Carlo (MC) simulation to study the charge-carrier mobility in an amorphous layer—typically 100 nm thick—that contains well-ordered nanosized domains (crystallites). The case of a low carrier concentration, typical for applications in photovoltaics and LEDs, is considered. We study the dependence of mobility on temperature, on the amount (V) of the crystallites, on the energy offset between crystalline and amorphous regions (Et), and we compare the results with those for a system with solitary traps. We find that, in a system with solitary traps, the mobility can exceed that of the neat phase if the trap depth is comparable with the standard deviation of the density of states (DOS) of the amorphous phase. Controlled by the electronic overlap in the amorphous phase and the crystallites, the mobility in a system with crystallites can increase by up to two orders of magnitude upon increasing V. It features a pronounced maximum when Et is close to the standard deviation of the DOS of the amorphous phase, while for large values of Et, the mobility is practically independent of Et. The results can be rationalized in terms of an interplay between percolation at large Et and hopping transport within the cumulative densities near the transport of the system. We developed a generalized analytic multiple-trapping-release model to rationalize the results of the MC simulations.

In recent years, record efficiencies of halide perovskite-based devices have been achieved by processing high-quality thin films, where small morphology differences seem to be relevant for optimized optoelectronic functionality. However, a detailed understanding on how small morphological changes in perovskite films affect their structural and optoelectronic properties is still missing. Here, we investigate the influence of small morphology differences (i.e., increased grain size and crystallographic orientation), which are induced by hot-pressing methylammonium lead iodide (MAPbI3) thin films, on the structural properties, phase transition behavior, energetic disorder, and defects. To this end, detailed temperature-dependent photoluminescence (PL) and absorption analyses from 300 K down to 5 K are performed. The morphology differences, confirmed by scanning electron microscopy and X-ray diffractometry analyses, result in an increased phase transition temperature for hot-pressed (HP) films, which we attribute to less strain. Moreover, fluence-dependent and transient PL measurements reveal a lower defect density in HP films. Here, besides grain size, also the degree of orientation appears to enhance the charge carrier lifetimes. The identified interdependence of strain and defect properties with film morphology suggests small differences in the perovskite’s energetic disorder. Our work thus emphasizes the importance that even small structural differences in halide perovskites have on their optoelectronic functionality, spurring their further optimization.

Preparing halide perovskite films by solvent-free, powder-based processing approaches currently attracts more and more attention. However, working solar cells employing dry, powder-based halide perovskite thin films, have not been demonstrated so far. Herein, perovskite solar cells are presented where the absorber layer is prepared by transferring readily synthesized perovskite powders into a compact thin film using a fully dry-powder-processing concept. Compact thin films are deposited via an optimized powder aerosol deposition (PAD) process. Pressing at 120 °C further improves the morphology and the optoelectronic film properties. Integrating the perovskite films in a solar cell configuration results in fully working devices, with champion power conversion efficiencies of >6%. While the (optoelectronic) properties of the PAD-processed films are found to be comparable with their solution-processed counterparts, investigations of the solar cell stack suggest deterioration of the electron-transport layer properties due to the PAD process, and the presence of hydrates at the perovskite surface to be important factors that contribute to the limited solar cell efficiency. Herein, perspectives to overcome the identified limitations are outlined, emphasizing the high potential and realizability of efficient perovskite solar cells based on dry-powder-processing approaches in the future.

In an endeavor to understand why the dissociation of charge-transfer (CT) states in a PM6:Y6 solar-cell is not a thermally activated process, measurements of energy-resolved impedance as well as of intrinsic photoconduction are employed. This study determines the density of states distributions of the pertinent HOMO and LUMO states and obtains a Coulomb binding energy (Eb,CT) of ≈150 meV. This is 250 meV lower than the value expected for a pair of localized charges with 1 nm separation. The reason is that the hole is delocalized in the polymer and the electron is shared among Y6 molecules forming a J-like aggregate. There are two key reasons why this binding energy of the CT state is not reflected in the temperature dependence of the photocurrent of PM6:Y6-diode: i) The e–h dissociation in a disordered system is a multi-step process whose activation energy is principally different from the binding energy of the CT state and can be substantially less than Eb,CT, and ii) since dissociation of the CT state competes with its intrinsic decay, the dissociation yield saturates once the rate of dissociation grossly exceeds the rate of intrinsic decay. This study argues that these conditions are met in a PM6:Y6-solar cell.

Unraveling the dominant charge transport mechanism in high-mobility amorphous oxide semiconductors is still a matter of controversy. In the present study we extended the random band-edge model suggested before for the charge transport and Hall-effect mobility in such disordered materials [Fishchuk et al., Phys. Rev. B 93, 195204 (2016)], and also describe the field-effect-modulated thermoelectricity in amorphous In-Ga-Zn-O (a-IGZO) films under the same premises. The model is based on the concept of charge transport through the extended states and assumes that the transport is limited by the spatial variation of the position of the band edge due to the disorder potential, rather than by localized states. The theoretical model is formulated using the effective medium approximation framework and describes well basic features of the Seebeck coefficient in disordered materials as a function of energy disorder, carrier concentration, and temperature. Carrier concentration dependencies of power factor and thermoelectric figure of merit have been also considered for such systems. Besides, our calculations reveal a remarkable turnover effect from a negative to a positive temperature dependence of Seebeck coefficient upon increasing carrier concentration. The suggested unified model provides a good quantitative description of available experimental data on the Seebeck coefficient and the charge mobilities measured in the same a-IGZO transistor as a function of the gate voltage and temperature by considering the same charge transport mechanisms. This promotes a deeper understanding and a more credible and accurate description of the transport process in a-IGZO films.

The development of efficient blue donor–acceptor thermally activated delayed fluorescence (TADF) emitters remains a challenge. To enhance the efficiency of TADF-related processes of the emitter, we targeted a molecular design that would introduce a large number of intermediate triplet states between the lowest energy excited triplet (T1) and singlet (S1) excited states. Here, we introduce an oligomer approach using repetitive donor–acceptor units to gradually increase the number of quasi-degenerate states. In our design, benzonitrile (BN) moieties were selected as acceptors that are connected together via the amine donors, acting as bridges to adjacent BN acceptors. To preserve the photoluminescence emission wavelength across the series, we employed a design based on an ortho substitution pattern of the donors about the BN acceptor that induces a highly twisted conformation of the emitters, limiting the conjugation. Via a systematic photophysical study, we show that increasing the oligomer size allows for enhancement of the intersystem crossing and reverse intersystem crossing rates. We attribute the increasing intersystem crossing rate to the increasing number of intermediate triplet states along the series, confirmed by the time-dependent density functional theory. Overall, we report an approach to enhance the efficiency of TADF-related processes without changing the blue photoluminescence color.

The dynamics of charge carriers in disordered organic semiconductors is inherently difficult to probe by spectroscopic methods. Thermally stimulated luminescence (TSL) is an approach that detects the luminescence resulting from the recombination of spatially-well-separated geminate charge pairs, usually at low temperature. In this way, the density of states (DOS) for charges can be determined. In this study, we demonstrate that TSL can also be used for probing an occupied density of states formed by a low-temperature energetic relaxation of photogenerated charges. Another approach used to gain an insight into the charge-relaxation process is kinetic Monte Carlo (KMC) simulations. Here, we use both techniques to determine the energetic distribution of charges at low temperatures. We find that the charge dynamics is frustrated, yet this frustration can be overcome in TSL by using an infrared (IR) push pulse, and in KMC simulations by a long simulation time that allows for long-range tunneling. Applying the IR-push TSL to pristine amorphous films of 18 commonly used low-molecular-weight organic light-emitting diode materials, we find that the width of the occupied DOS amounts to about 2/3 of the available DOS. The same result is obtained in KMC simulations that consider spatial correlations between site energies. Without the explicit consideration of energetic correlations, the experimental values cannot be reproduced, which testifies to the importance of spatial correlations for charges.

Within the last few years, applying pressure to improve and alter the structural and optoelectronic properties of halide perovskite thin films and powder-based thick-film pellets has emerged as a promising processing method. However, a detailed understanding of the relationship between perovskite microstructure, pressing process, and final film properties is still missing. Here, we investigate the impact of powder microstructure on the compaction processes during pressure treatment and on the final properties of powder-pressed thick films, using the model halide perovskite methylammonium lead iodide (MAPbI3). Analyzing pressure relaxations together with XRD and SEM characterizations, we find that larger powder particles result in less compact thick films with higher surface roughness. Furthermore, larger particles exhibit stronger sintered connections between individual powder particles, resulting in less crushing and particle rearrangement but in more pronounced plastic deformation during pressure treatment. Moreover, plastic deformation of the powder particles leads to a reduction of crystallite size in the final film. This reduction results in increased nonradiative, defect-associated excited state recombination, as confirmed by photoluminescence investigations. More plastic deformation also deteriorates the grain boundary quality and consequently facilitates ion migration, which is reflected in higher electrical dark conductivities of the thick films. Thus, our work elucidates how important the design of the perovskite powder microstructure is for the pressure-induced compaction behavior and for the resulting structural, optical, and electrical thick-film properties. These insights will pave the way for tailored pressure processing of halide perovskite films with improved optoelectronic properties.

In organic solar cells, the resulting device efficiency depends strongly on the local morphology and intermolecular interactions of the blend film. Optical spectroscopy was used to identify the spectral signatures of interacting chromophores in blend films of the donor polymer PM6 with two state-of-the-art nonfullerene acceptors, Y6 and N4, which differ merely in the branching point of the side chain. From temperature-dependent absorption and luminescence spectroscopy in solution, it is inferred that both acceptor materials form two types of aggregates that differ in their interaction energy. Y6 forms an aggregate with a predominant J-type character in solution, while for N4 molecules the interaction is predominantly in a H-like manner in solution and freshly spin-cast film, yet the molecules reorient with respect to each other with time or thermal annealing to adopt a more J-type interaction. The different aggregation behavior of the acceptor materials is also reflected in the blend films and accounts for the different solar cell efficiencies reported with the two blends.

While using additives such as ionic liquids (IL) is known to boost the efficiency and stability of perovskite solar cells, it is still unclear how ILs impact the difficile perovskite film formation process. Here we investigate the impact of the IL BMIMBF4 on the film formation of the model halide perovskite MAPbI3 by multimodal optical in situ spectroscopy during solution processing via one-step spin coating and a solvent engineering approach. One-step processing experiments reveal that IL in the precursor solutions does not affect the formation of perovskite–solvent complexes, but higher IL contents delay the perovskite transformation with decreased growth rates. For solvent engineering, the perovskite growth rate decreases with later anti-solvent (AS) dripping as the properties of PbI42− species in the precursor solutions change during drying. Here the IL also affects the evolution of the PbI42− properties, as the IL cation interacts with the PbI42−. This interaction appears to reduce the perovskite growth rates after initiating perovskite formation by AS dripping. Still, in the as-coated films the IL efficiently passivates defect states. Thus, our work provides important insights into how decisive ILs impact the sensitive interconnection between precursor properties, film formation process and final optoelectronic functionality of perovskite thin films.

Copper salts are a popular choice as p-dopants for organic semiconductors, particularly in N2,N2,N2′,N2′,N7,N7,N7′,N7′-octakis(4-methoxyphenyl)-9,9′-spirobi[9H-fluoren]-2,2′,7,7′-tetramine (Spiro-MeOTAD) hole transport material for solar cells. While being exceptionally effective, no scientific consensus about their doping mechanism has been established so far. This study describes the thermodynamic equilibria of involved species in copper(II) bis(trifluoromethanesulfonyl)imide (Cu(TFSI)2) doped, co-evaporated Spiro-MeOTAD. A temperature-independent formation of charge transfer states is found, followed by an endothermic release of free charge carriers. Impedance and electron paramagnetic resonance spectroscopy unravel low activation energies for hole release and hopping transport. As a result, (52.0 ± 6.4)% of the total Cu(TFSI)2 molecules form free, dissociated holes at 10 mol% and room temperature. CuI species arising out of doping are stabilized by formation of a [CuI(TFSI)2]- cuprate, inhibiting elemental copper formation. This CuI species presents a potent hole trap reducing their mobility, which can be averted by simple addition of a bathocuproine complexing agent. A nonlinear temperature-dependent conductivity and mobility that contradicts current charge transport models is observed. This is attributed to a combination of trap- and charge transfer state freeze-out. These insights may be adapted to other metal salts, providing guidelines for designing next-generation ultra-high efficiency dopants.

The development of high-performance solution-processed organic light-emitting diodes (OLEDs) remains a challenge. An effective solution, highlighted in this work, is to use highly efficient thermally activated delayed fluorescence (TADF) dendrimers as emitters. Here, the design, synthesis, density functional theory (DFT) modeling, and photophysics of three triazine-based dendrimers, tBuCz2pTRZ, tBuCz2mTRZ, and tBuCz2m2pTRZ, is reported, which resolve the conflicting requirements of achieving simultaneously a small ΔEST and a large oscillator strength by incorporating both meta- and para-connected donor dendrons about a central triazine acceptor. The solution-processed OLED containing a host-free emitting layer exhibits an excellent maximum external quantum efficiency (EQEmax) of 28.7%, a current efficiency of 98.8 cd A−1, and a power efficiency of 91.3 lm W−1. The device emits with an electroluminescence maximum, λEL, of 540 nm and Commission International de l’Éclairage (CIE) color coordinates of (0.37, 0.57). This represents the most efficient host-free solution-processed OLED reported to date. Further optimization directed at improving the charge balance within the device results in an emissive layer containing 30 wt% OXD-7, which leads to an OLED with the similar EQEmax of 28.4% but showing a significantly improved efficiency rolloff where the EQE remains high at 22.7% at a luminance of 500 cd m−2.

The potential of dendrimers exhibiting thermally activated delayed fluorescence (TADF) as emitters in solution-processed organic light-emitting diodes (OLEDs) has to date not yet been realized. This in part is due to a poor understanding of the structure–property relationship in dendrimers where reports of detailed photophysical characterization and mechanism studies are lacking. In this report, using absorption and solvatochromic photoluminescence studies in solution, the origin and character of the lowest excited electronic states in dendrimers with multiple dendritic electron-donating moieties connected to a central electron-withdrawing core via a para- or a meta-phenylene bridge is probed. Characterization of host-free OLEDs reveals the superiority of meta-linked dendrimers as compared to the already reported para-analogue. Comparative temperature-dependent time-resolved solid-state photoluminescence measurements and quantum chemical studies explore the effect of the substitution mode on the TADF properties and the reverse intersystem crossing (RISC) mechanism, respectively. For TADF dendrimers with similarly small ∆EST, it is observed that RISC can be enhanced by the regiochemistry of the donor dendrons due to control of the reorganization energies, which is a heretofore unexploited strategy that is distinct from the involvement of intermediate triplet states through a nonadiabatic (vibronic) coupling with the lowest singlet charge transfer state.

Since the key role of charge transfers (CT) states has been identified for organic solar cells (OSCs), research into their properties is a timely topic. Conventionally, their absorption and emission spectra are described in terms of Marcus’ electron transfer theory. This is a single site approach with the essential parameter being the reorganization energy. Thus, it ignores ensemble effects, notably the role of static disorder that is inevitably present in a spin-coated OSC film. Here time dependent photoluminescence spectroscopy is applied on blends of the polymeric donor MeLPPP with either the non-fullerene acceptor SF-PDI2 or with PC61BM within a temperature range from 295 to 5 K. The authors monitor how initially excited singlet states are converted to emissive CT states. Concomitantly, emission from residual singlets on the acceptor is observed rather than hybrid CT-states. The role of spectral diffusion in this process is discussed. From the temperature and time dependent linewidths of absorption, fluorescence, and CT emission, the static and dynamic contributions to the total disorder are inferred. In both blends, at 295 K, the contribution of static disorder is comparable to the dynamic disorder.

Non-fullerene acceptors (NFAs) as used in state-of-the-art organic solar cells feature highly crystalline layers that go along with low energetic disorder. Here, the crucial role of energetic disorder in blends of the donor polymer PM6 with two Y-series NFAs, Y6, and N4 is studied. By performing temperature-dependent charge transport and recombination studies, a consistent picture of the shape of the density of state distributions for free charges in the two blends is developed, allowing an analytical description of the dependence of the open-circuit voltage VOC on temperature and illumination intensity. Disorder is found to influence the value of the VOC at room temperature, but also its progression with temperature. Here, the PM6:Y6 blend benefits substantially from its narrower state distributions. The analysis also shows that the energy of the equilibrated free charge population is well below the energy of the NFA singlet excitons for both blends and possibly below the energy of the populated charge transfer manifold, indicating a down-hill driving force for free charge formation. It is concluded that energetic disorder of charge-separated states has to be considered in the analysis of the photovoltaic properties, even for the more ordered PM6:Y6 blend.

Thermally activated delayed fluorescence (TADF) relies on a small energy gap between the emissive singlet and the non-emissive triplet state, obtained by reducing the wavefunction overlap between donor and acceptor moieties. Efficient emission, however, requires maintaining a good oscillator strength, which is itself based on sufficient overlap of the wavefunctions between donor and acceptor moieties. We demonstrate an approach to subtly fine-tune the required wavefunction overlap by employing donor-dendrons of changing functionality. We use a carbazolyl-phthalonitrile based donor-acceptor core, 2CzPN, as a reference emitter, and progressively localize the hole density through substitution at the 3,6-positions of the carbazole donors (Cz) with further carbazole, (4-tert-butylphenyl)amine (tBuDPA) and phenoxazine (PXZ). Using detailed photoluminescence studies, complemented with Density Functional Theory (DFT) calculations, we show that this approach permits a gradual decrease of the singlet-triplet gap, ΔEST, from 300 meV to around 10 meV in toluene, yet we also demonstrate why a small ΔEST alone is not enough. While sufficient oscillator strength is maintained with the Cz- and tBuDPA-based donor dendrons, this is not the case for the PXZ-based donor dendron, where the wavefunction overlap is reduced too strongly. Overall, we find the donor-dendron extension approach allows successful fine-tuning of the emitter photoluminescence properties.

The development of efficient blue emitter–host combinations is one of the biggest challenges in organic light-emitting diode (OLED) research. Host materials play a crucial role when it comes to enhancing the efficiency, improving the lifetime and decreasing the efficiency roll-off of the device. The need for new hosts is of prime importance, especially for blue phosphorescence and thermally activated delayed fluorescence (TADF) emitters, due to their high exciton energies. The hosts are less investigated than the emitters and require further progress. This work provides a new molecular strategy that combines an acridine derivative (donor) and pyrimidine moieties (acceptors) to obtain three novel host materials. This approach demonstrates that via careful selection of donor and acceptor units, it is possible to manage the properties of the host materials, obtaining at the same time superior thermal and morphological properties and high triplet energies up to 3.07 eV. The decrease of the conjugation in the acceptor unit was found to play a crucial role in increasing the triplet energy. The most promising host 1MPA was used to fabricate blue TADF OLEDs. Using a sky-blue emitter, we achieved electroluminescence at 491 nm and a maximum external quantum efficiency (EQE) of 13.6%, combined with a low efficiency roll-off, even beyond the practical brightness of 1000 cd m−1. The host 1MPA was also combined with a deep blue emitter to deliver a blue OLED with color coordinates of x = 0.16 and y = 0.18.

The powder aerosol deposition (PAD) method is becoming increasingly important as an energetically advantageous coating method compared to classic ceramic technologies. However, due to the process-related lattice deformation, ceramic coatings often exhibit reduced functional properties in the as-deposited state. A thermal posttreatment at temperatures well below the sintering temperature can significantly reduce the lattice deformation and the stress within the film to restore the functional film properties close to sintered bulk samples. In this work, the optothermal posttreatment of PAD films using three different high-power light emitting diodes (HP-LED) with different wavelengths within the visible light spectrum is investigated as an alternative to time-consuming furnace or energy-intensive laser processes on the example of thermoelectric CuFe0.98Sn0.02O2 films. We demonstrate that the space-saving LED-based posttreatment not only restores the film properties but also significantly reduces the required processing time to a few seconds.

We employ photoluminescence (PL) spectroscopy on individual nanoscale aggregates of the conjugated polymer poly(3-hexylthiophene), P3HT, at room temperature (RT) and at low temperature (LT) (1.5 K), to unravel different levels of structural and electronic disorder within P3HT nanoparticles. The aggregates are prepared by self-assembly of the block copolymer P3HT-block-poly(ethylene glycol) (P3HT-b-PEG) into micelles, with the P3HT aggregates constituting the micelles’ core. Irrespective of temperature, we find from the intensity ratio between the 0–1 and 0–0 peaks in the PL spectra that the P3HT aggregates are of H-type nature, as expected from π-stacked conjugated thiophene backbones. Moreover, the distributions of the PL peak ratios demonstrate a large variation of disorder between micelles (inter-aggregate disorder) and within individual aggregates (intra-aggregate disorder). Upon cooling from RT to LT, the PL spectra red-shift by 550 cm–1, and the energy of the (effective) carbon-bond stretch mode is reduced by 100 cm–1. These spectral changes indicate that the P3HT backbone in the P3HT-b-PEG copolymer does not fully planarize before aggregation at RT and that upon cooling, partial planarization occurs. This intra-chain torsional disorder is ultimately responsible for the intra- and inter-aggregate disorder. These findings are supported by temperature-dependent absorption spectra on thin P3HT films. The interplay between intra-chain, intra-aggregate, and inter-aggregate disorder is key for the bulk photophysical properties of nanoparticles based on conjugated polymers, for example, in hierarchical (super-) structures. Ultimately, these properties determine the usefulness of such structures in hybrid organic–inorganic materials, for example, in (bio-)sensing and optoelectronics applications.

The active element of an organic field effect transistor (OFET) is a polycrystalline transport layer. The crystallites are interrupted by grain boundaries (GB) that can act as traps or barriers to the charge‐carriers. Their impact on charge transport and hence on the performance of the OFET is still not fully understood. Employing kinetic Monte Carlo studies, the authors set up well‐defined test systems and explore how the parameters of the system, for example, the thickness of the GB, their fractional contribution to the overall film, and the energies of the GB relative to the crystallites, affect the performance of the OFET. It is found that these parameters control the position of the Fermi level, which is crucial in controlling whether the charge transport is confined to GB, or whether it takes place as a superposition between filamentary transport in the boundaries and delocalized transport in the crystallites, or as tunneling‐mediated transport across the crystallites. Guidelines for the morphological optimization of the films for these different transport modes are derived.

The electronic density of states (DOS) plays a central role in controlling the charge-carrier transport
in amorphous organic semiconductors, while its accurate determination is still a challenging task.
We apply the low-temperature fractional thermally stimulated luminescence (TSL) technique to determine
the DOS of pristine amorphous films of organic light-emitting diode (OLED) host materials.
The DOS width is determined for two series of hosts, namely, (i) carbazole-biphenyl derivatives, 4,4-
bis(N-carbazolyl)-1,1-biphenyl (CBP), 3,3-di(9H-carbazol-9-yl)-1,1-biphenyl (mCBP), and 3,5-di(9Hcarbazol-
9-yl)-[1,1-biphenyl]-3-carbonitrile (mCBP-CN), and (ii) carbazole-phenyl (CP) derivatives,
1,3-bis(N-carbazolyl)benzene (mCP) and 9-[3-(9H-carbazol-9-yl)phenyl]-9H-carbazole-3-carbonitrile
(mCP-CN). TSL originates from radiative recombination of charge carriers thermally released from the
lower-energy part of the intrinsic DOS that causes charge trapping at very low temperatures. We find that
the intrinsic DOS can be approximated by a Gaussian distribution, with a deep exponential tail accompanying
this distribution in CBP and mCBP films. The DOS profile broadens with increasing molecular
dipole moments, varying from 0 to 6 D, in a similar manner within each series, in line with the dipolar disorder
model. The same molecular dipole moment, however, leads to a broader DOS of CP compared with
CBP derivatives. Using computer simulations, we attribute the difference between the series to a smaller
polarizability of cations in CP derivatives, leading to weaker screening of the electrostatic disorder by
induction. These results demonstrate that the low-temperature TSL technique can be used as an efficient
experimental tool for probing the DOS in small-molecule OLED materials

While it is commonly accepted that the activation energy of the thermally activated polaron hopping transport in disordered organic semiconductors can be decoupled into a disorder and a polaron contribution, their relative weight is still controversial. This feature is quantified in terms of the so-called C factor in the expression for the effective polaron mobility: μe∝exp[−Ea/kBT−C(σ/kBT)2], where Ea and σ are the polaron activation energy and the energy width of a Gaussian density of states (DOS), respectively. A key issue is whether the universal scaling relation (implying a constant C factor) regarding the polaron formation energy is really obeyed, as recently claimed in the literature [Seki and Wojcik, J. Chem. Phys. 145, 034106 (2016)]. In the present work, we reinvestigate this issue on the basis of the Marcus transition rate model using extensive kinetic Monte Carlo simulations as a benchmark tool. We compare the polaron-transport simulation data with results of analytical calculations by the effective medium approximation and multiple trapping and release approaches. The key result of this study is that the C factor for Marcus polaron hopping depends on first the degree of carrier localization, i.e., the coupling between the sites, further whether quasiequilibrium has indeed been reached, and finally the σ/Ea ratio. This implies that there is no universal scaling with respect to the relative contribution of polaron and disorder effect. Finally, we demonstrate that virtually the same values of the disorder parameter σ are determined from available experimental data using the C factors obtained here irrespective of whether the data are interpreted in terms of Marcus or Miller-Abrahams rates. This implies that molecular reorganization contributes only weakly to charge transport, and it justifies the use of the zero-order Miller-Abrahams rate model for evaluating the DOS width from temperature-dependent charge transport measurements regardless of whether or not polaron effects are accounted for.

Efficient triplet exciton hopping (diffusion) in amorphous solid films is essential for triplet–triplet annihilation (TTA) and TTA-mediated photon upconversion (UC) at low excitation power densities. However, enhanced triplet diffusion, particularly in high-emitter-content UC films, also facilitates their trapping and quenching at nonradiative decay sites, thus deteriorating UC efficiency. In this work, triplet exciton diffusion and quenching are studied in matrix-free solid UC films based on two novel bisfluorene-anthracene (BFA) emitters, i.e., one with methyl substitution (BFA-Me) and the other with a phenyl substitution (BFA-Ph), and a standard platinum octaethylporphyrin (PtOEP) sensitizer. By analyzing temperature-dependent TTA-UC dynamics and accounting for various singlet exciton-related processes, we are able to discern triplet exciton quenching occurring explicitly in the emitter and show that it is one of the dominating mechanisms impeding the UC performance of BFA/PtOEP films, particularly at elevated temperatures. Regardless of the lower density of quenchers present in the BFA-Ph film, twice as large triplet diffusivity estimated in this film (D = (2.13 ± 0.64) × 10–9 cm2·s–1) at room temperature as compared to that in the BFA-Me film caused more rapid triplet quenching. This resulted in the shifting of the optimal UC performance of BFA-Ph to lower temperatures (T = 160 K) with respect to that of BFA-Me (T = 220 K). To obtain a high UC quantum yield, which for these materials can be estimated to reach >5% at room temperature and above, the excessive diffusion to the remaining quenching sites needs to be suppressed, e.g., by increasing the intermolecular distance through side groups.

Although the density of states (DOS) distribution of charge transporting states in an organic semiconductor is vital for device operation, its experimental assessment is not at all straightforward. In this work, the technique of energy resolved–electrochemical impedance spectroscopy (ER‐EIS) is employed to determine the DOS distributions of valence (highest occupied molecular orbital (HOMO)) as well as electron (lowest unoccupied molecular orbital (LUMO)) states in several organic semiconductors in the form of neat and blended films. In all cases, the core of the inferred DOS distributions are Gaussians that sometimes carry low energy tails. A comparison of the HOMO and LUMO DOS of P3HT inferred from ER‐EIS and photoemission (PE) or inverse PE (IPE) spectroscopy indicates that the PE/IPE spectra are by a factor of 2–3 broader than the ER‐EIS spectra, implying that they overestimate the width of the distributions. A comparison of neat films of MeLPPP and SF‐PDI2 or PC(61)BM with corresponding blends reveals an increased width of the DOS in the blends. The results demonstrate that this technique does not only allow mapping the DOS distributions over five orders of magnitude and over a wide energy window of 7 eV, but can also delineate changes that occur upon blending.

In this work, we present a versatile approach to achieve well-defined conjugated polymers and oligomers from a single standard synthesis route via preparative size-exclusion chromatography. Using a special recycle mode and well-defined endcappers, we are able to prepare pure oligomers with three to eight repeat units and high-molecular-weight polymers with dispersity ĐM as low as 1.06 in just one preparation step with reasonable yield. To demonstrate the capabilities of our method, we conducted a fundamental spectroscopic study on the influence of chain length and molecular weight distribution on electronic properties and aggregation behavior of a series of fluorene based oligo- and polymers. Due to the well-defined nature of the investigated compounds, we consistently find a first-order phase transition and an increase of the critical transition temperature from the amorphous phase to the ordered β-phase as a function of the number of repeat units in accordance with the Sanchez model on coil–globule transitions.

Conjugated polymers and oligomers that emit polarized light are used as active materials in various optoelectronic device applications, notably organic light-emitting diodes (OLEDs). Here, we demonstrate the fabrication of electrospun polarized light-emitting fibers from a non-conjugated polymer that can be aligned by a simple heat-stretching process. Upon excitation at 340 nm, ribbons made from the nanofibers show polarized deep blue luminescence with an anisotropy of 0.37 and a quantum yield of about 31%. Furthermore, they exhibit room temperature green phosphorescence with a lifetime of about 200 ms as well as a delayed deep blue fluorescence resulting from triplet–triplet annihilation (non-coherent photon upconversion) (TTA). Wide and small angle X-ray scattering experiments show that the stretched electrospun fibers are highly aligned with nearly perfect uniaxial orientation within the fabricated ribbons. This results in a mechanically robust and flexible material, with a high specific tensile strength (534 ± 28) MPa cm3 g−1 and toughness (79 ± 7) J g−1. The combination of efficient polarized deep blue luminescence, room temperature phosphorescence, TTA, mechanical robustness and flexibility of these fibers opens up new avenues for applications of non-conjugated polymers.

The performance of solution-processed organic semiconductor devices is heavily influenced by the morphology of the active layer. Film formation is a complex process, with the final morphology being the result of the interplay between processing parameters and molecular properties, which is only poorly understood. Here, we investigate the influence of molecular stiffness by using two model oligomers, TT and CT, which differ only in the rotational flexibility of their central building block. We monitor absorption and emission simultaneously in situ during spin coating. We find that film formation takes place in four similar stages for both compounds. However, the time scales are remarkably different during the third stage, where electronically interacting aggregates are created. While this process is fast for the stiff CT, it takes minutes for the flexible TT. By comparing with previously determined aggregation properties in solution, we conclude that even though aggregate formation concurs with a planarization process, a certain amount of backbone flexibility is beneficial for establishing ordered structures during film formation. Here, the elongated time window in the case of the flexible compound can further allow for better processing control.

It is well known that in organic solids the collision of two excitons can give rise to delayed fluorescence (DF). Revived interest in this topic is stimulated by the current endeavor towards the development of efficient organic optoelectronic devices such as organic light-emitting diodes (OLEDs) and solar cells, or sensitizers used in photodynamic therapy. In such devices, triplet excitations are ubiquitously present but their annihilations can be either detrimental, e.g., giving rise to a roll-off of intensity in an OLED, or mandatory, e.g., if the sensitizer relies on up-conversion of long-lived low-energy triplet excitations. Since the employed materials are usually noncrystalline, optical excitations migrate via incoherent hopping. Here, we employ kinetic Monte Carlo simulations (KMC) to study the complex interplay of triplet-triplet annihilation (TTA) and quenching of the triplet excitations by impurities in a single-component system featuring a Gaussian energy landscape and variable system parameters such as the length of the hopping sites, i.e., a conjugated oligomer, the morphology of the system, the degree of disorder (σ), the concentration of triplet excitations, and temperature. We also explore the effect of polaronic contributions to the hopping rates. A key conclusion is that the DF features a maximum at a temperature that scales with σ/kBT. This is related to disorder-induced filamentary currents and thus locally enhanced triplet densities. We predict that a maximum for the TTA process near room temperature or above requires typically a disorder parameter of at least 70 meV.

An easy-to-access, near-UV-emitting linearly extended B,N-doped heptacene with high thermal stability is designed and synthesized in good yields. This compound exhibits thermally activated delayed fluorescence (TADF) at ambient temperature from a multiresonant (MR) state and represents a rare example of a non-triangulene-based MR-TADF emitter. At lower temperatures triplet–triplet annihilation dominates. The compound simultaneously possesses narrow, deep-blue emission with CIE coordinates of (0.17, 0.01). While delayed fluorescence results mainly from triplet–triplet annihilation at lower temperatures in THF solution, where aggregates form upon cooling, the TADF mechanism takes over around room temperature in solution when the aggregates dissolve or when the compound is well dispersed in a solid matrix. The potential of our molecular design to trigger TADF in larger acenes is demonstrated through the accurate prediction of ΔEST using correlated wave-function-based calculations. On the basis of these calculations, we predicted dramatically different optoelectronic behavior in terms of both ΔEST and the optical energy gap of two constitutional isomers where only the boron and nitrogen positions change. A comprehensive structural, optoelectronic, and theoretical investigation is presented. In addition, the ability of the achiral molecule to assemble on a Au(111) surface to a highly ordered layer composed of enantiomorphic domains of racemic entities is demonstrated by scanning tunneling microscopy.

Six luminophores bearing an OBO-fused benzo[fg]tetracene core as an electron acceptor were designed and synthesized. The molecular structures of three molecules (PXZ-OBO, 5PXZ-OBO, 5DMAC-OBO) were determined by single crystal X-ray diffraction studies and revealed significant torsion between the donor moieties and the OBO acceptor with dihedral angles between 75.5 and 86.2°. Photophysical studies demonstrate that blue and deep blue emission can be realized with photoluminescence maxima (λPL) ranging from 415 to 480 nm in mCP films. The emission energy is modulated by simply varying the strength of the donor heterocycle, the number of donors, and their position relative to the acceptor. Although the DMAC derivatives show negligible delayed emission because of their large singlet-triplet excited state energy difference, ΔEST, PXZ-based molecules, especially PXZ-OBO with an experimental ΔEST of 0.25 eV, demonstrate delayed emission in blend mCP films at room temperature, which suggests triplet exciton harvesting occurs in these samples, potentially by thermally activated delayed fluorescence.

The synthesis of stable blue TADF emitters and the corresponding matrix materials is one of the biggest challenges in the development of novel OLED materials. We present six bipolar host materials based on triazine as an acceptor and two types of donors, namely, carbazole, and acridine. Using a tool box approach, the chemical structure of the materials is changed in a systematic way. Both the carbazole and acridine donor are connected to the triazine acceptor via a para- or a meta-linked phenyl ring or are linked directly to each other. The photophysics of the materials has been investigated in detail by absorption-, fluorescence-, and phosphorescence spectroscopy in solution. In addition, a number of DFT calculations have been made which result in a deeper understanding of the photophysics. The presence of a phenyl bridge between donor and acceptor cores leads to a considerable decrease of the triplet energy due to extension of the overlap electron and hole orbitals over the triazine-phenyl core of the molecule. This decrease is more pronounced for the para-phenylene than for the meta-phenylene linker. Only direct connection of the donor group to the triazine core provides a high energy of the triplet state of 2.97 eV for the carbazole derivative CTRZ and 3.07 eV for the acridine ATRZ. This is a major requirement for the use of the materials as a host for blue TADF emitters.

Ordered domains play a central role in determining the properties of organic semiconductors, and thereby the performance of their devices. The molecules in these ordered domains are often characterized by planar backbone conformations. We investigate the influence of backbone planarity on the propensity to form ordered structures using a pair of model oligomers with electron poor benzothiadiazole moieties and electron rich thiophene units. The two oligomers differ by their central unit, where a bithiophene unit either allows for flexible twists (“TT”), or where it is bridged as a cyclopentadithiophene to provide a rigid planar connection (“CT”). Temperature dependent absorption and luminescence spectroscopy in solution along with atomistic simulations show that the more flexible TT readily forms aggregates upon cooling, while CT instead first forms non-emissive excimers and only forms aggregates below 200 K. Molecular dynamics simulations reveal that aggregation in TT can only be accounted for if TT takes on a planar conformation in the course of the aggregation process. The stronger intermolecular interaction in TT compared to the banana-shaped CT can then be related to the larger number of attractive intermolecular interactions between the various subunits. Thus, molecular flexibility is an important design parameter, as it determines the accessibility of ordered intermolecular structures and ultimately device performance.

A new design strategy is introduced to address a persistent weakness with resonance thermally activated delayed fluorescence (R‐TADF) emitters to reduce aggregation‐caused quenching effects, which are identified as one of the key limiting factors. The emitter Mes3DiKTa shows an improved photoluminescence quantum yield of 80% compared to 75% for the reference DiKTa in 3.5 wt% 1,3‐bis(N‐carbazolyl)benzene. Importantly, emission from aggregates, even at high doping concentrations, is eliminated and aggregation‐caused quenching is strongly curtailed. For both molecules, triplets are almost quantitatively upconverted into singlets in electroluminescence, despite a significant (≈0.21 eV) singlet‐triplet energy gap (ΔEST), in line with correlated quantum‐chemical calculations, and a slow reverse intersystem crossing. It is speculated that the lattice stiffness responsible for the narrow fluorescence and phosphorescence emission spectra also protects the triplets against nonradiative decay. An improved maximum external quantum efficiencies (EQEmax) of 21.1% for Mes3DIKTa compared to the parent DiKTa (14.7%) and, importantly, reduced efficiency roll‐off compared to literature resonance TADF organic light‐emitting diodes (OLEDs), shows the promise of this design strategy for future design of R‐TADF emitters for OLED applications.

Carbene‐metal‐amides (CMAs) are a promising family of donor–bridge–acceptor molecular charge‐transfer (CT) emitters for organic light‐emitting diodes. A universal approach is demonstrated to tune the energy of their CT emission. A blueshift of up to 210 meV is achievable in solid state via dilution in a polar host matrix. The origin of this shift has two components: constraint of thermally‐activated triplet diffusion, and electrostatic interactions between guest and polar host. This allows the emission of mid‐green CMA archetypes to be tuned to sky blue without chemical modifications. Monte‐Carlo simulations based on a Marcus‐type transfer integral successfully reproduce the concentration‐ and temperature‐dependent triplet diffusion process, revealing a substantial shift in the ensemble density of states in polar hosts. In gold‐bridged CMAs, this shift does not lead to a significant change in luminescence lifetime, thermal activation energy, reorganization energy, or intersystem crossing rate. These discoveries offer new insight into coupling between the singlet and triplet manifolds in CMA materials, revealing a dominant interaction between states of CT character. The same approach is employed using materials which have been chemically modified to alter the energy of their CT state directly, shifting the emission of sky‐blue chromophores into the practical blue range.

In this report, we investigate the binding properties of the Lewis acid tris(pentafluorophenyl)borane with a Lewis base semiconducting polymer, PFPT, and the subsequent mechanism of band gap reduction. Experiments and quantum chemical calculations confirm that the formation of a Lewis acid adduct is energetically favorable (ΔG° < −0.2 eV), with preferential binding at the pyridyl nitrogen in the polymer backbone over other Lewis base sites. Upon adduct formation, ultraviolet photoelectron spectroscopy indicates only a slight decrease in the HOMO energy, implying that a larger reduction in the LUMO energy is primarily responsible for the observed optical band gap narrowing (ΔEopt = 0.3 eV). Herein, we also provide the first spatially resolved picture of how Lewis acid adducts form in heterogeneous, disordered polymer/tris(pentafluorophenyl)borane thin films via one- (1D) and two-dimensional (2D) solid-state nuclear magnetic resonance. Notably, solid-state 1D 11B, 13C{1H}, and 13C{19F} cross-polarization magic-angle spinning (CP-MAS) NMR and 2D 1H{19F} and 1H{1H} correlation NMR analyses establish that BCF molecules are intercalated between branched C16H33 side chains with the boron atom facing toward the pyridyl nitrogen atoms of PFPT.

A new design strategy is introduced to address a persistent weakness with resonance thermally activated delayed fluorescence (R-TADF) emitters to reduce aggregation-caused quenching effects, which are identified as one of the key limiting factors. The emitter Mes3DiKTa shows an improved photoluminescence quantum yield of 80% compared to 75% for the reference DiKTa in 3.5 wt% 1,3-bis(N-carbazolyl)benzene. Importantly, emission from aggregates, even at high doping concentrations, is eliminated and aggregation-caused quenching is strongly curtailed. For both molecules, triplets are almost quantitatively upconverted into singlets in electroluminescence, despite a significant (≈0.21 eV) singlet-triplet energy gap (ΔEST), in line with correlated quantum-chemical calculations, and a slow reverse intersystem crossing. It is speculated that the lattice stiffness responsible for the narrow fluorescence and phosphorescence emission spectra also protects the triplets against nonradiative decay. An improved maximum external quantum efficiencies (EQEmax) of 21.1% for Mes3DIKTa compared to the parent DiKTa (14.7%) and, importantly, reduced efficiency roll-off compared to literature resonance TADF organic light-emitting diodes (OLEDs), shows the promise of this design strategy for future design of R-TADF emitters for OLED applications.

We investigate the combined influence of energetic disorder and delocalization on electron–hole charge-transfer state separation efficiency in donor–acceptor organic photovoltaic systems using an analytical hopping model and Monte Carlo calculations, coupled with an effective mass model. Whereas energetic disorder increases the separation yield at intermediate and low electric fields for low-efficiency blends with strongly localized carriers, we find that it reduces dramatically the fill factors and power conversion efficiencies in high-efficiency solar cells that require high carrier delocalization within the conjugated segment and high mobility–lifetime product. We further demonstrate that the initial electron–hole distance and thermalization processes play only a minor role in the separation dynamics.

The fundamental nature of charge transport in highly ordered organic semiconductors is under constant debate. At cryogenic temperatures, effects within the semiconductor such as traps or the interaction of charge car-riers with the insulating substrate (dipolar disorder or Fröhlich polarons) are known to limit carrier motion. In comparison, at elevated temperatures, where charge carrier mobility often also decreases as function of temperature, phonon scattering or dynamic disorder are frequently discussed mechanisms, but the exact microscopic cause that limits carrier motion is debated. Here, the mobility in the temperature range between 200 and 420 K as function of carrier density is explored in highly ordered perylene-diimide from 3 to 9 nm thin films. It is observed that above room temperature increasing the gate electric field or decreasing the semiconducting film thickness leads to a sup-pression of the charge carrier mobility. Via X-ray diffraction measurements at various temperatures and electric fields, changes of the thin film structure are excluded as cause for the observed mobility decrease. The experimental findings point toward scattering sites or traps at the semiconductor–dielectric interface, or in the dielectric as limiting factor for carrier mobility, whose role is usually neglected at elevated temperatures.

The Meyer-Neldel (MN) compensation rule, implying an exponential increase in the prefactor with increasing activation energy in a thermally activated process, is naturally emerging in two-site transition rates as a result of multiphonon excitation processes. However, it has been recently demonstrated [Phys. Rev. B. 90, 245201 (2014)] that the experimentally observed compensation behavior for the temperature-activated charge transport in thin-film organic field-effect transistors (OFETs) is not a genuine phenomenon, but rather it is an apparent extrapolated effect that arises as a consequence of the partial filling of the Gaussian DOS distribution. To resolve the contradiction, we investigate the impact of different jump-rate models on macroscopic hopping-charge transport in a random organic system using an effective medium analytic approach. The principal result of this study is that the averaging over the individual jump rates in a conventional Gaussian disordered system erodes the genuine thermodynamically determined MN compensation effect, and therefore, the macroscopic transport no longer reflects the microscopic rates. The apparent compensation behavior observed for OFET mobilities upon varying the carrier concentrations can be reproduced regardless of the single-phonon or multiphonon character of activated transitions. Another remarkable finding is that the disorder formalism does predict a genuine MN compensation effect using multiphonon rates if a disordered semiconductor contains a significant concentration of deep traps, so that the cumulative DOS features a double-peak Gaussian. Thus, this study bridges the gap between Gaussian disorder and multi-excitation entropy (MEE) models concerning the MN effect, and has important implications for the interpretation of the isokinetic MN temperature in disordered organic semiconductors.

We investigate the aggregation behaviour of the donor-acceptor molecules p-DTS(FBTTh2)2 (“T1”) and p SIDT(FBTTh2)2 (“H1”) in MTHF solutions. Using optical spectroscopy, we find that T1 forms aggregates in solution while H1 aggregates only when processed as a thin film, but not in solution. Free energy molecular dynamics (MD) simulations based on force-fields derived from quantum-mechanical density functional theory fully reproduce this difference. Our simulations reveal that this difference is not due to the lengthy carbon side chains. Rather, the molecular symmetry of T1 allows for an aggregated state in which the central donor units are spatially well separated while a similar configuration is sterically impossible for H1. As a consequence, any aggregation of H1 necessarily involves aggregation of the central donors which requires, as a first step, stripping the central donor of its protective MTHF solvation shell. This unfavourable process leads to a significant kinetic hindrance for aggregation and explain the strongly differing aggregation behaviour of T1/H1 in MTHF despite their otherwise similar structure. By comparison to further donor-acceptor molecules with structure and symmetry similar to T1 and H1, referred to as CT and TT, respectively, we demonstrate that this aggregation behaviour results from the individual building blocks of the systems in question and is thus of a more general nature. Our results give insights for the design molecules with a specific…..

It is shown that simple bilayer devices consisting of the diketopyrrolopyrrole (DPP) monomer Ph‐TDPP‐Ph as donor and C60 as acceptor feature J–V‐characteristics of a bidirectional organic phototransistor where illumination intensity plays the role of the gate voltage as compared to a conventional field‐effect transistor. The output current may therefore be controlled both electrically and optically. The underlying mechanism is based on the good charge transport in Ph‐TDPP‐Ph and C60, the intrinsic dissociation properties of C60, and the presence of an injection barrier for holes. In addition to this, it is demonstrated that the observed behavior of the DPP/C60 system allows the realization of basic logic elements like NOT‐, AND‐, and OR‐Gates, which may provide the basis for advanced analog and digital applications.

We use bilayer devices with a series of three fullerene acceptors differing in order and intermolecular coupling to systematically explore the influence of electron delocalization in the acceptor phase on the dissociation efficiency of charge transfer states. Structural information from GIWAXS measurements is combined with the results of optical and electrical characterization as well as theoretical modeling. Our results indicate that an increase in CT-dissociation efficiency is directly coupled to an enhancement in electron delocalization that is particularly prominent for C60 which forms crystalline domains. Therefore, our results substantiate the concept of delocalization of electrons taking a positive role in the charge separation process, and of acceptor crystallinity being crucial in this respect.

Here, we report the synthesis, optical properties, and solid‐state packing of monodisperse oligomers of diketopyrrolopyrrole (DPP) up to five repeating units. The optical properties of DPP oligomers in solution and the solid state were investigated by a combination of steady‐state and transient spectroscopy. Transient absorption spectroscopy and time‐correlated single photon counting (TCSPC) measurements show that the fluorescence lifetime decreases with an increase in the oligomer size from monomer to trimer, thereby reaching saturation for pentameric DPP oligomers. The solid‐state packing and crystallinity were probed by using advanced techniques, which included grazing incidence small‐angle X‐ray scattering (GISAXS) and X‐ray diffraction (XRD) to elucidate the structure–property trend. Collectively, our chain‐length dependent studies establish the fundamental correlation between the structure and property and provide a comprehensive understanding of the solid‐state properties in DPP–DPP based conjugated systems.

Charge-carrier mobility has been investigated by time-of-flight (TOF) transient photocurrent in a lateral transport configuration in highly crystalline thin films of 2,7-dioctyl[1]benzothieno [3,2-b][1] benzothiophene (C8-BTBT) grown by a zone-casting alignment technique. High TOF mobility has been revealed that it is consistent with the delocalized nature of the charge transport in this material, yet it featured a positive temperature dependence at T≥295K. Moreover, the mobility was surprisingly found to decrease with electric field in the high-temperature region. These observations are not compatible with the conventional band-transport mechanism. We have elaborated an analytic model based on effective-medium approximation to rationalize the puzzling findings. The model considers the delocalized charge transport within the energy landscape formed by long-range transport band-edge variations in imperfect organic crystalline materials and accounts for the field-dependent effective dimensionality of charge transport percolative paths. The results of the model calculations are found to be in good agreement with experimental data.

The Frenkel-Holstein model in the Born-Oppenheimer regime is used to interpret temperature-dependent photoluminescence spectra of solutions made with the poly(p-phenylene vinylene) derivative MEH-PPV. Using our recently developed structural optimization method and assuming only intrachain electronic coupling, we predict the structure of emissive MEH-PPV chromophores in terms of a mean torsional angle ϕ0 and its static fluctuations σϕ, assuming no cis-trans defects. This allows us to fully account for the observed changes in spectra, and the chromophore structures obtained are consistent with the known phase transition at 180 K between a “red” and “blue” phase.

We developed a novel all-optical method for monitoring the diffusion of a small quencher molecule through a polymer layer in a bilayer architecture. Experimentally, we injected C60 molecules from a C60 layer into the adjacent donor layer by stepwise heating, and we measured how the photoluminescence (PL) of the donor layer becomes gradually quenched by the incoming C60 molecules. By analyzing the temporal evolution of the PL, the diffusion coefficient of C60 can be extracted, as well as its activation energy and an approximate concentration profile in the film. We applied this technique to three carbazole-based low-bandgap polymers with different glass temperatures with a view to study the impact of structural changes of the polymer matrix on the diffusion process. We find that C60 diffusion is thermally activated and not driven by WFL-type collective motion above Tg but rather by local motions mediated by the sidechains. The results are useful as guidance for material design and device engineering, and the approach can be adapted to a wide range of donor and acceptor materials.

The aim of the present work is to identify the appropriate framework for analyzing photoluminescence and photocurrent (EQE) spectra of charge transfer (CT) states in donor–acceptor blends used as active materials for organic solar cells. It was stimulated by the work of Vandewal et al. (J. Am. Chem. Soc., 2017, 139(4), 1699–1704) who analyzed EQE spectra of CT states of a series of blend systems in terms of Marcus theory assuming that, first, the spectral shape reflects the reorganization energy of the donor upon ionization and, second, that disorder effects are unimportant. To test this assumption we applied gated photoluminescence (PL) spectroscopy within a temperature range from 5 to 295 K combined with EQE as well as electroluminescence (EL) experiments on 1 : 1 Me-LPPP : PCBM blends by weight. We find that the PL spectra are virtually temperature independent and the temporal decay of the emission features a power law with an exponent close to −3/2 as Hong and Noolandi predicted for distributed geminately bound electron-holes pairs. The EL spectrum reveals a red-shift by 100 meV relative to the PL spectrum. The results are inconsistent with both Marcus’ electron transfer theory and the original Marcus–Levich–Jortner (MLJ) theory, and they prove that disorder effects are crucial. Both PL and EQE spectra can be rationalized in terms of the classic Franck–Condon picture of electronic transitions that couple to intra-molecular vibrations as well as low frequency modes of the donor–acceptor pair that forms the CT state.

We investigate the impact of excess PbI2 in the precursor solution on the structural and optical properties of thin films of the model hybrid perovskite methylammonium lead iodide (MAPbI3). We find that excess of PbI2 in the precursor solution results in crystalline PbI2 in the final thin film that is located at the grain boundaries. From UPS we find that this crystalline PbI2 phase has no direct impact on the electronic structure of MAPbI3. In contrast to this, temperature dependent absorption measurements indicate a systematic change in the temperature dependence of the exciton binding energy in the perovskite. We also observe a decrease in the critical temperature and a concomitant smearing out of the tetragonal–orthorhombic phase transition as a function of excess PbI2. Our results thus help to better understand the exact role of PbI2 in the perovskite layer and pave the way for a more tailored design of perovskite solar cells.

We use a Frenkel–Holstein model of uncoupled chains in the adiabatic limit to simulate the optical spectra of the conjugated polymer ladder-type poly(p-phenylene) derivative (MeLPPP), which is a planar conjugated polymer with especially low interchain interactions. The theoretical calculations correctly reproduce the vibronic spectra and yield reasonable torsion angles between adjacent phenyl rings. The success of this approach indicates that, in contrast to interchain coupling, the strong electronic coupling along a polymer chain is more appropriately described in the adiabatic limit.

The backbone conformation of conjugated polymers affects, to a large extent, their optical and electronic properties. The usually flexible substituents provide solubility and influence the packing behavior of conjugated polymers in films or in bad solvents. However, the role of the side chains in determining and potentially controlling the backbone conformation, and thus the optical and electronic properties on the single polymer level, is currently under debate. Here, we investigate directly the impact of the side chains by studying the bulky-substituted poly(3-(2,5-dioctylphenyl)thiophene) (PDOPT) and the common poly(3-hexylthiophene) (P3HT), both with a defined molecular weight and high regioregularity, using low-temperature single-chain photoluminescence (PL) spectroscopy and quantum-classical simulations. Surprisingly, the optical transition energy of PDOPT is significantly (∼2,000 cm−1 or 0.25 eV) red-shifted relative to P3HT despite a higher static and dynamic disorder in the former. We ascribe this red shift to a side-chain induced backbone planarization in PDOPT, supported by temperature-dependent ensemble PL spectroscopy. Our atomistic simulations reveal that the bulkier 2,5-dioctylphenyl side chains of PDOPT adopt a clear secondary helical structural motif and thus protect conjugation, i.e., enforce backbone planarity, whereas, for P3HT, this is not the case. These different degrees of planarity in both thiophenes do not result in different conjugation lengths, which we found to be similar. It is rather the stronger electronic coupling between the repeating units in the more planar PDOPT which gives rise to the observed spectral red shift as well as to a reduced calculated electron−hole polarization.

A spin-crossover coordination polymer [Fe(L1)(bipy)]n (where L = a N2O22– coordinating Schiff base-like ligand bearing a phenazine fluorophore and bipy = 4,4′-bipyridine) was synthesized and exhibits a 48 K wide thermal hysteresis above room temperature (T1/2↑ = 371 K and T1/2↓ = 323 K) that is stable for several cycles. The spin transition was characterized using magnetic measurements, Mössbauer spectroscopy, and DSC measurements. T-dependent X-ray powder diffraction reveals a structural phase transition coupled with the spin transition phenomenon. The dimeric excerpt {(μ-bipy)[FeL1(MeOH)]2}·2MeOH of the coordination polymer chain crystallizes in the triclinic space group P1̅ and reveals that the packing of the molecules in the crystal is dominated by hydrogen bonds. Investigation of the emission properties of the complexes with regard to temperature shows that the spin crossover can be tracked by monitoring the emission spectra, since the emission color changes from greenish to a yellow color upon the low spin-to-high spin transition.

Aggregates – that is short-ranged ordered moieties in the solid-state of π-conjugated polymers – play an important role in the photophysics and performance of various optoelectronic devices. We have previously shown that many polymers change from a disordered to a more ordered conformation when cooling a solution below a characteristic critical temperature math formula. Using in situ time-resolved absorption spectroscopy on the prototypical semiconducting polymers P3HT, PFO, PCPDTBT, and PCE11 (PffBT4T-2OD), we show that spin-coating at a temperature below math formula can enhance the formation of aggregates with strong intra-chain coupling. An analysis of their time-resolved spectra indicates that the formation of nuclei in the initial stages of film formation for substrates held below math formula seems responsible for this. We observe that the growth rate of the aggregates is thermally activated with an energy of 310 meV, which is much more than that of the solvent viscosity (100 meV). From this we conclude that the rate controlling step is the planarization of a chain that is associated with its attachment to a nucleation center. The success of our approach for the rather dynamic deposition method of spin-coating holds promise for other solution-based deposition methods

Here, we report the synthesis, optical properties, and solid-state packing of monodisperse oligomers of diketopyrrolopyrrole (DPP) up to five repeating units. The optical properties of DPP oligomers in solution and the solid state were investigated by a combination of steady-state and transient spectroscopy. Transient absorption spectroscopy and time-correlated single photon counting (TCSPC) measurements show that the fluorescence lifetime decreases with an increase in the oligomer size from monomer to trimer, thereby reaching saturation for pentameric DPP oligomers. The solid-state packing and crystallinity were probed by using advanced techniques, which included grazing incidence small-angle X-ray scattering (GISAXS) and X-ray diffraction (XRD) to elucidate the structure–property trend. Collectively, our chain-length dependent studies establish the fundamental correlation between the structure and property and provide a comprehensive understanding of the solid-state properties in DPP–DPP based conjugated systems.

We discuss whether electron transfer from a photoexcited polymer donor to a fullerene acceptor in an organic solar cell is tractable in terms of Marcus theory, and whether the driving force ΔG0 is crucial in this process. Considering that Marcus rates are presumed to be thermally activated, we measured the appearance time of the polaron (i.e., the radical-cation) signal between 12 and 295 K for the representative donor polymers PTB7, PCPDTBT, and Me-LPPP in a blend with PCBM as acceptor. In all cases, the dissociation process was completed within the temporal resolution of our experimental setup (220–400 fs), suggesting that the charge transfer is independent of ΔG0. We find that for the PCPDTBT:PCBM (ΔG0 ≈ −0.2 eV) and PTB7:PCBM (ΔG0 ≈ −0.3 eV) the data is mathematically consistent with Marcus theory, yet the condition of thermal equilibrium is not satisfied. For MeLPPP:PCBM, for which electron transfer occurs in the inverted regime (ΔG0 ≈ −1.1 eV), the dissociation rate is inconsistent with Marcus theory but formally tractable using the Marcus–Levich–Jortner tunneling formalism which also requires thermal equilibrium. This is inconsistent with the short transfer times we observed and implies that coherent effects need to be considered. Our results imply that any dependence of the total yield of the photogeneration process must be ascribed to the secondary escape of the initially generated charge transfer state from its Coulomb potential.

We demonstrate that the degree of charge delocalization has a strong impact on polarization energy and thereby on the position of the transport band edge in organic semiconductors. This gives rise to long-range potential fluctuations, which govern the electronic transport through delocalized states in organic crystalline layers. This concept is employed to formulate an analytic model that explains a negative field dependence coupled with a positive temperature dependence of the charge mobility observed by a lateral time-of-flight technique in a high-mobility crystalline organic layer. This has important implications for the further understanding of the charge transport via delocalized states in organic semiconductors.

We investigate the excited state dynamics and the conformation of a new molecular donor-bridge-acceptor system, a Cu(II)-phthalocyanine (CuPc) covalently linked via a flexible aliphatic spacer to a perylenebisimide (PBI). We performed time-resolved polarization anisotropy and pump-probe measurements in combination with molecular dynamics simulations. Our data suggest the existence of three conformations of the dyad: two more extended, metastable conformations with centre-of-mass distances > 1 nm between the PBI and CuPc units of the dyad, and a highly stable folded structure, in which the PBI and CuPc units are stacked on top of each other with a centre-of-mass distance of 0.4 nm. In the extended conformation the dyad shows emission predominantly from the PBI unit with a very weak contribution from the CuPc unit. In contrast, for the folded conformation the PBI emission of the dyad is strongly quenched due to fast energy transfer from the PBI to the CuPc unit (3 ps) and subsequent intersystem-crossing (300 fs) from the first excited singlet state of CuPc unit into its triplet state. Finally, the CuPc triplet state is deactivated non-radiatively with a time constant of 25 ns.

The field of conjugated polymers has expanded in the last years considerably and impressive performance, both in field effect transistors and photovoltaic devices has been achieved. After the initial emphasis on improving the performance, more emphasis is recently given to fundamental studies on structure formation. Therefore, this review concentrates on systematic correlation studies of structure formation in solution, in bulk and thin films as well as in photovoltaic blends of donor-type π-conjugated polymers. The main focus is on the correlation of structure, morphology and molecular chain orientation as a function of macromolecular properties such as molecular weight, dispersity, non-covalent intramolecular and intermolecular interactions, solvent interactions and innovative processing techniques. The tools applied for elucidating fundamental information of structure formation and orientation mainly consist of optical spectroscopy and scattering techniques (SAXS/WAXS/GIWAXS). Since the field of conjugated polymers is very vast in terms of chemical structural diversity, only selected examples of donor polymers are covered here and the emerging class of n-type conjugated polymers are not included. The focus is not on the structural variation or their performance in solar cells or transistors in terms of record efficiencies, but on the systematic studies leading to a structure-property correlation in donor polymers.

In this study, we report a detailed spectroscopic study concerning the energy levels and vibrational structure of thiophene–pyrrole-containing S,N-heteroacenes. The aim of the study is first, to understand the differences in the photoluminescence (PL) efficiencies in this structurally similar series and second, to compare the electronic structure of S,N-heteroacenes to that of linear acenes and phenacenes, with a view to derive guidelines for the design of singlet fission materials. For S,N-heteroacenes comprising seven fused heterocyclic rings, we observe a higher PL quantum yield for derivatives with terminal thienothiophene units than for thienopyrrole-capped ones. This is assigned to a stronger tendency of the thienopyrrole-capped derivatives to form nonemissive associates in dilute solution, producing emissive excimers at higher concentration. By conducting time-resolved PL studies at 77 K, we further determine the lowest singlet and triplet energies for the S,N-heteroacenes with three, five, and seven fused rings. We show that their energies evolve with oligomer length analogously to those of phenacenes, yet in a fundamentally different way from that of linear acenes. This difference in evolution is attributed to the increasingly biradical character in acenes with increasing chain length in contrast to the S,N-heteroacenes and phenacenes.

A novel family of S,N-heteroheptacenes SN7a–d with a variable thiophene–pyrrole ratio and a heteroring fusion sequence is presented. All SN7-derivatives can be synthesized in efficient multi-step synthetic routes with good overall yields. The crucial cyclization step to the stable and soluble fused systems is achieved by multiple Pd-catalyzed Buchwald–Hartwig aminations or C–S coupling reaction in high yields. The comparison of the optoelectronic properties provides interesting structure–property relationships and gives valuable insights into the role of nitrogen atoms within the series of thiophene–pyrrole containing S,N-heteroheptacenes. Remarkable differences in emission behaviour and noticeable correlations of the oxidation potentials of the S,N-heteroheptacenes offer helpful information for the construction of other heteroacenes. Additionally, UV-Vis-NIR absorption spectra of the corresponding radical cations generated by chemical oxidation were monitored and compared.

We demonstrate that efficient and nearly field-independent charge separation of electron–hole pairs in organic planar heterojunction solar cells can be described by an incoherent hopping mechanism. Using kinetic Monte Carlo simulations that include the effect of on-chain delocalization as well as entropic contributions, we simulate the dissociation of the charge-transfer state in polymer–fullerene bilayer solar cells. The model further explains experimental results of almost field independent charge separation in bilayers of molecular systems with fullerenes and provides important guidelines at the molecular level for maximizing the efficiencies of organic solar cells. Thus, utilizing coherent phenomena is not necessarily required for highly efficient charge separation in organic solar cells.

Organic solar cells (OSCs) have achieved much attention and meanwhile reach efficiencies above 10%. One problem yet to be solved is the lack of long term stability. Crosslinking is presented as a tool to increase the stability of OSCs. A number of materials used for the crosslinking of bulk heterojunction cells are presented. These include the crosslinking of low bandgap polymers used as donors in bulk heterojunction cells, as well as the crosslinking of fullerene acceptors and crosslinking between donor and acceptor. External crosslinkers often based on multifunctional azides are also discussed. In the second part, some work either leading to OSCs with high efficiencies or giving insight into the chemistry and physics of crosslinking are highlighted. The diffusion of low molar mass fullerenes in a crosslinked matrix of a conjugated polymer and the influence of crosslinking on the carrier mobility is discussed. Finally, the use of crosslinking to make stable interlayers and the solution processing of multilayer OSCs are discussed in addition to presentation of a novel approach to stabilize nanoimprinted patterns for OSCs by crosslinking.

We present a detailed spectroscopic study, along with the synthesis, of conjugated, ladder-type 2,7-linked poly(pyrene)s. We observe a delocalization of the first singlet excited state along the polymer backbone, i.e., across the 2,7 linkage in the pyrene moiety, in contrast to earlier studies on conjugated 2,7-linked poly(pyrene)s without ladder structure. The electronic signature of the pyrene unit is, however, manifested in an increased lifetime and reduced oscillator strength as well as a modified vibronic progression in absorption of the singlet state compared to a ladder-type poly(para-phenylene) (MeLPPP). Furthermore, the reduced oscillator strength and increased lifetime slow down Förster-type energy transfer in films, where this transfer occurs to sites with increasing inter-chain coupling of H-type nature.

We suggest an analytic theory based on the effective medium approximation (EMA) which is able to describe
charge-carrier transport in a disordered semiconductor with a significant degree of degeneration realized at high
carrier concentrations, especially relevant in some thin-film transistors (TFTs), when the Fermi level is very
close to the conduction-band edge. The EMA model is based on special averaging of the Fermi-Dirac carrier
distributions using a suitably normalized cumulative density-of-state distribution that includes both delocalized
states and the localized states. The principal advantage of the present model is its ability to describe universally
effective drift and Hall mobility in heterogeneous materials as a function of disorder, temperature, and carrier
concentration within the same theoretical formalism. It also bridges a gap between hopping and bandlike
transport in an energetically heterogeneous system. The key assumption of the model is that the charge carriers
move through delocalized states and that, in addition to the tail of the localized states, the disorder can give rise
to spatial energy variation of the transport-band edge being described by a Gaussian distribution. It can explain
a puzzling observation of activated and carrier-concentration-dependent Hall mobility in a disordered system
featuring an ideal Hall effect. The present model has been successfully applied to describe experimental results
on the charge transport measured in an amorphous oxide semiconductor, In-Ga-Zn-O (a-IGZO). In particular, the
model reproduces well both the conventional Meyer-Neldel (MN) compensation behavior for the charge-carrier
mobility and inverse-MN effect for the conductivity observed in the same a-IGZO TFT. The model was further
supported by ab initio calculations revealing that the amorphization of IGZO gives rise to variation of the
conduction-band edge rather than to the creation of localized states. The obtained changes agree with the one
we used to describe the charge transport. We found that the band-edge variation dominates the charge transport
in high-quality a-IGZO TFTs in the above-threshold voltage region, whereas the localized states need not to be
invoked to account for the experimental results in this material.

Carrier mobility is a key parameter for the application of conjugated polymers. In this work, a series of polyfluorenes (PF2/6) with different fractions of crosslinkable acrylate groups is investigated. Mobility measurements are carried out to assess the influence of crosslinking with different photoinitiators on the performance of the material. For the regime of low to medium charge carrier density, relevant for OLEDs and OPVs, we used a novel technique based on the injection of charge carriers from the electrodes of an optoelectronic device: MIS-CELIV (MIS: metal-insulator-semiconductor). For large charge carrier densities we performed OFET measurements. We find that using optimized conditions crosslinking does not influence the hole mobility in the investigated system. Furthermore, we demonstrate that the crosslinking process may be triggered solely by thermal activation and UV-illumination without the need of any initiator. Thus, densely crosslinked networks are obtained without the formation of undesired decomposition products from added photoinitiator.

The aggregation of π-conjugated materials significantly impacts the photophysics and performance of optoelectronic devices. Nevertheless, little is known about the laws governing aggregate formation of π-conjugated materials from solution. In this Perspective, we compare, discuss, and summarize how aggregates form for three different types of compounds, that is, homopolymers, donor–acceptor type polymers, and low molecular weight compounds. To this end, we employ temperature-dependent optical spectroscopy, which is a simple yet powerful tool to investigate aggregate formation. We show how optical spectra can be analyzed to identify distinct conformational states. We find aggregate formation to proceed the same in all these compounds by a coil-to-globule-like first-order phase transition. Notably, the chain expands before it collapses into a highly ordered dense state. The role of side chains and the impact of changes in environmental polarization are addressed.

While it has been argued that field-dependent geminate pair recombination (GR) is important, this process is often disregarded when analyzing the recombination kinetics in bulk heterojunction organic solar cells (OSCs). To differentiate between the contributions of GR and nongeminate recombination (NGR) the authors study bilayer OSCs using either a PCDTBT-type polymer layer with a thickness from 14 to 66 nm or a 60 nm thick p-DTS(FBTTh2)2 layer as donor material and C60 as acceptor. The authors measure JV-characteristics as a function of intensity and charge-extraction-by-linearly-increasing-voltage-type hole mobilities. The experiments have been complemented by Monte Carlo simulations. The authors find that fill factor (FF) decreases with increasing donor layer thickness (Lp) even at the lowest light intensities where geminate recombination dominates. The authors interpret this in terms of thickness dependent back diffusion of holes toward their siblings at the donor–acceptor interface that are already beyond the Langevin capture sphere rather than to charge accumulation at the donor–acceptor interface. This effect is absent in the p-DTS(FBTTh2)2 diode in which the hole mobility is by two orders of magnitude higher. At higher light intensities, NGR occurs as evidenced by the evolution of s-shape of the JV-curves and the concomitant additional decrease of the FF with increasing layer thickness.

In an endeavor to examine how optical excitation of C60 and PCBM contribute to the photogeneration of charge carriers in organic solar cells, we investigated stationary photogeneration in single-layer C60 and PCBM films over a broad spectrum as a function of the electric field. We find that intrinsic photogeneration starts at a photon energy of about 2.25 eV, i.e., about 0.4 eV above the first singlet excited state. It originates from charge transfer type states that can autoionize before relaxing to the lower-energy singlet S1 state, in the spirit of Onsager’s 1938 theory. We analyze the internal quantum efficiency as a function of electric field and photon energy to determine (1) the Coulombic binding and separation of the electron–hole pairs, (2) the value of the electrical gap, and (3) which fraction of photoexcitations can fully separate at a given photon energy. The latter depends on the coupling between the photogenerated charge transfer states and the eventual charge transporting states. It is by a factor of 3 lower in PCBM. Close to the threshold energy for intrinsic photoconduction (2.25 eV), the generating entity is a photogenerated electron–hole pair with roughly 2 nm separation. At higher photon energy, more expanded pairs are produced incoherently via thermalization.

A critical issue of bulk heterojunction (BHJ) solar cells is the instability of the morphology of the polymer:fullerene blend over long operation times. We report the synthesis of crosslinkable derivatives of the low bandgap polymer PFDTBT, poly(2,7-(9,9-dialkylfluorene)-alt-(5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole))), and the stabilization of BHJ solar cells by crosslinking. Oxetane units are attached to the polymer side chains as crosslinkable functional groups. We study the crosslinking of the polymers via cationic ring opening polymerization of the oxetanes and show that our materials rapidly form insoluble networks. Our materials also crosslink in the presence of fullerenes. We report for the first time that crosslinking takes place upon prolonged heating to 100 °C without any added initiator. The best efficiency and thermal stability are found in thermally crosslinked BHJ solar cells. After 30 hours at 100 °C, 65% of the initial efficiency are retained and no further decay is observed up to 100 hours.

We present a number of polyfluorene based conjugated polymers with crosslinkable acrylate and oxetane units. These
polymers can be crosslinked by free radical polymerization in the case of acrylates and by cationic ring opening
polymerization for oxetanes. Upon polymerization densely crosslinked networks are formed which are completely
insoluble. We show that the diffusion coefficient of C60 in polyfluorene is reduced by a factor of 1000 by crosslinking.
MIS-CELIV measurements are used to monitor changes in the charge carrier mobility upon crosslinking. It shows that
using appropriate conditions, e.g. low initiator concentrations or thermal crosslinking, the charge carrier mobility is not
reduced by crosslinking. Solution processed three layer organic solar cells were realized with a crosslinkable fluorene
based copolymer containing acrylate groups. The efficiency is increased from 1.4% for the reference to 1.8% in the three
layer cell with a crosslinked exciton blocking layer. A critical issue of BHJ cells is the instability of the morphology of
the polymer:fullerene blend over long operation times at elevated temperature. We present a crosslinkable derivative of
the low bandgap polymer PFDTBT which contains oxetane units. BHJ cells with the crosslinked PFDTBT derivative and
PCBM were tested in accelerated aging experiments at 100 °C for times up to 100 h. Stabilization was clearly observed
in crosslinked BHJ cells compared to the non-crosslinked reference. We show for the first time that oxetane containing
polymers can be thermally crosslinked without any added initiator. Initiator free crosslinking is particularly attractive as
it avoids the formation of decomposition products, and thus potential electron traps and quenching sites from the
initiator.

Inorganic-organic halide organometal perovskites have demonstrated very promising performance for opto-electronic applications, such as solar cells, light-emitting diodes, lasers, single-photon sources, etc. However, the little knowledge on the underlying photophysics, especially on a microscopic scale, hampers the further improvement of devices based on this material. In this communication, correlated conventional photoluminescence (PL) characterization and wide-field PL imaging as a function of time are employed to investigate the spatially- and temporally-resolved PL in CH3NH3PbI3−xClx perovskite films. Along with a continuous increase of the PL intensity during light soaking, we also observe PL blinking or PL intermittency behavior in individual grains of these films. Combined with significant suppression of PL blinking in perovskite films coated with a phenyl-C61-butyric acid methyl ester (PCBM) layer, it suggests that this PL intermittency is attributed to Auger recombination induced by photoionized defects/traps or mobile ions within grains. These defects/traps are detrimental for light conversion and can be effectively passivated by the PCBM layer. This finding paves the way to provide a guideline on the further improvement of perovskite opto-electronic devices.

A series of organosulfur-functionalized trans-platinum(II) bis(alkenylarylalkynyl) complexes, having one
tolylthio moiety in each alkenyl backbone with general formula trans-[(PEt3)2Pt{C^C-Ar-CH]
CH(SC6H4eCH3)}2], (2ae2d), (where, Ar ¼ phenylene, biphenylene, 2,5-dimethylphenylene, and 2,5-
dimethoxyphenylene) were synthesized in good to excellent yields with good regioselectivity. As
compared to the absorption band of trans-platinum(II) bis(alkynylarylalkynyl) complexes, we found that
the position of the lowest energy absorption bands in the trans-platinum(II) bis(alkenylarylalkynyl)
complexes were red-shifted, after the functionalization of the trans-platinum(II) bis(alkynylarylalkynyl)
complexes with arylthiol. For all trans-platinum(II) complexes, the lowest energy absorption bands in the
UV/Vis spectra, in chloroform solution, at room temperature, were observed in the range 362e394 nm,
and under excitation at the wavelength of the absorption maximum exhibited the emission peak
maximum at room temperature in the range 401e426 nm. The newly synthesized complexes are not
exhibited phosphorescence at room temperature but are exhibited at low temperature, 77 K. All the new
platinum(II) complexes have been fully characterized by spectroscopic analysis as well as elemental
analysis, and the trans square-planar arrangement at the platinum centre has been confirmed by singlecrystal
X-ray diffraction study of complex 2a

We have investigated how the addition of 1,8-diiodooctane (DIO) alters the formation of disordered and ordered phases in a film of poly(3-hexyl-thiophene-2,5-diyl) (P3HT). By combining in situ time-resolved absorption spectroscopy with 60 ms time resolution, optical and transmission electron microscopy and spatially resolved photoluminescence spectroscopy, we show that, in addition to the excitonic coupling, the film formation process during spin-coating as well as the subsequent long-time film drying process differ significantly when DIO is added to a solution of P3HT. During spin-coating, the addition of DIO reduces the actual time for transformation from disordered to ordered phase, even though it increases the time until the disorder–order transition sets in. In place of a solidification front, we observe an all-over solidification throughout the entire film. The phase separation between nonaggregated and aggregated phase increases when using DIO, with compositional variation in the content of aggregated phase on a micrometer scale.

We present a combined detailed spectroscopic and quantum chemical study on the bipolar host materials BPTRZ and MBPTRZ in solution and in neat film. In the two compounds, the hole transporting carbazole is separated from the electron transporting triazine moiety by a fully aromatic but non-conjugated meta-linked biphenyl unit. The two materials differ by an additional steric twist at the biphenyl in MBPTRZ, which is achieved by methyl-substitution in 2- and 2′-position of the biphenyl. We find that while the twist shifts the triplet state in MBPTRZ to higher energies (3.0 eV in solution) compared to BPTRZ (2.8 eV in solution), this also localizes electron density on the carbazole moiety, leading to excimer formation in neat films.

Electron transfer from an excited donor to an acceptor in an organic solar cell (OSC) is an exothermic
process, determined by the difference in the electronegativities of donor and acceptor. It has been
suggested that the associated excess energy facilitates the escape of the initially generated electron–
hole pair from their mutual coulomb well. Recent photocurrent excitation spectroscopy on conjugated
polymer/PCBM cells challenged this view. In this perspective we shall briefly outline the strengths and
weaknesses of relevant experimental approaches and concepts. We shall enforce the notion that the
charge separating state is a vibrationally cold charge transfer (CT) state. It can easily dissociate provided
that (i) there is electrostatic screening at the interface and (ii) the charge carriers are delocalized, e.g. if
the donor is a well ordered conjugated polymer. Both effects diminish the coulomb attraction and
assure that the in-built electric field existing in the OSC under short current condition is already
sufficient to separate most the CT states. The remaining CT excitations relax towards tail states of the
disorder controlled density of states distribution, such as excimer forming states, that are more tightly
bound and have longer lifetimes.

We show that the performance of an organic solar cell can be increased by the introduction of an additional polymeric exciton blocking layer. In order to realize this, the novel polymer PFTPDAc with pendant acrylate groups is developed. Thin films are coated from a PFTPDAc solution and subsequently crosslinked by irradiation. Thereby, the film becomes completely insoluble and allows spincoating of a second polymer layer on top. We realize a three layer solar cell which contains a crosslinked PFTPDAc interlayer on top of the molybdenum oxide anode and layers of the low-bandgap polymer PCDTBT and C60. In comparison with a reference cell without the interlayer the EQE is significantly increased in the spectral region between 400 nm and 650 nm. From current-voltage measurements a power conversion efficiency of 1.8% is determined. PL measurements show that the increase of solar cell performance is attributed to exciton blocking by the PFTPDAc interlayer.

The low-bandgap polymer poly{[4,4-bis(2-ethylhexyl)-cyclopenta-(2,1-b;3,4-b′)dithiophen]-2,6-diyl-alt-(2,1,3-benzo-thiadiazole)−4,7-diyl} (PCPDTBT) is widely used for organic solar cell applications. Here, we present a comprehensive study of the optical properties as a function of temperature for PCPDTBT in solution and in thin films with two distinct morphologies. Using absorption and photoluminescence spectroscopy as well as Franck-Condon analyses, we show that PCPDTBT in solution undergoes a phase transformation at 300 K from a disordered to a truly aggregated state on cooling. The saturation value of aggregates in solution is reached in PCPDTBT thin films at any temperature. In addition, we demonstrate that the photophysical properties of the aggregates in films are similar to those in solution and that a low percentage of thermally activated excimer states is present in the films at temperatures above 200 K.

The observation that in efficient organic solar cells almost all electron–hole pairs generated at the donor–acceptor interface escape from their mutual coulomb potential remains to be a conceptual challenge. It has been argued that it is the excess energy dissipated in the course of electron or hole transfer at the interface that assists this escape process. The current work demonstrates that this concept is unnecessary to explain the field dependence of electron–hole dissociation. It is based upon the formalism developed by Arkhipov and co-workers as well as Baranovskii and co-workers. The key idea is that the binding energy of the dissociating “cold” charge-transfer state is reduced by delocalization of the hole along the polymer chain, quantified in terms of an “effective mass”, as well as the fractional strength of dipoles existent at the interface in the dark. By covering a broad parameter space, we determine the conditions for efficient electron–hole dissociation. Spectroscopy of the charge-transfer state on bilayer solar cells as well as measurements of the field dependence of the dissociation yield over a broad temperature range support the theoretical predictions.

We present a spectroscopic investigation on the effect of changing the position where carbazole is attached to biphenyl in carbazolebiphenyl (CBP) on the triplet state energies and the propensity to excimer formation. For this, two CBP derivatives have been prepared with the carbazole moieties attached at the (para) 4- and 4′-positions (pCBP) and at the (meta) 3- and 3′-positions (mCBP) of the biphenyls. These compounds are compared to analogous mCDBP and pCDBP, i.e. two highly twisted carbazoledimethylbiphenyls, which have a high triplet energy at about 3.0 eV and tend to form triplet excimers in a neat film. This torsion in the structure is associated with localization of the excited state onto the carbazole moieties. We find that in mCBP and pCBP, excimer formation is prevented by localization of the triplet excited state onto the central moiety. As conjugation can continue from the central biphenyls into the nitrogen of the carbazole in the para-connected pCBP, emission involves mainly the benzidine. By contrast, the meta-linkage in mCBP limits conjugation to the central biphenyl. The associated shorter conjugation length is the reason for the higher triplet energy of 2.8 eV in mCBP compared with the 2.65 eV in pCBP.

Understanding the effects of aggregation on exciton relaxation and energy transfer is relevant to control photoinduced function in organic electronics and photovoltaics. Here, we explore the photoinduced dynamics in the low-temperature aggregated phase of a conjugated polymer by transient absorption and coherent electronic two-dimensional (2D) spectroscopy. Coherent 2D spectroscopy allows observing couplings among photoexcited states and discriminating band shifts from homogeneous broadening, additionally accessing the ultrafast dynamics at various excitation energies simultaneously with high spectral resolution. By combining the results of the two techniques, we differentiate between an initial exciton relaxation, which is not characterized by significant exciton mobility, and energy transport between different chromophores in the aggregate.

We have extended an effective medium approximation theory [Fishchuk, Kadashchuk, Genoe, Ullah, Sitter, Singh, Sariciftci, and Bässler, Phys. Rev. B 81, 045202 (2010)] to investigate how polaron formation affects the Meyer-Neldel (MN) compensation behavior observed for temperature-dependent charge-carrier transport in disordered organic semiconductors at large carrier concentrations, as realized in organic field-effect transistors (OFETs). We show that the compensation behavior in organic semiconductor thin films can be consistently described for both nonpolaronic and polaronic hopping transport in the framework of the disorder formalism using either Miller-Abrahams or polaron Marcus rates, respectively, provided that the polaron binding energy is small compared to the width of the density of states (DOS) distribution in the system. We argue that alternative models based on thermodynamic reasoning, like the multiexcitation entropy (MEE) model, which assumes charge transport dominated by polarons with multiphonon processes and ignores the energy disorder, are inherently not applicable to describe adequately the charge-carrier transport in disordered organic semiconductors. We have suggested and realized a test experiment based on measurements of the compensation behavior for the temperature-dependent conductivity and mobility in OFET devices to check the applicability of these models. We point out that the MN behavior observed in thin-film OFETs has nothing to do with the genuine MN rule predicted by the MEE approach, but rather it is an apparent effect arising as a consequence of the functional dependence of the partial filling of the DOS in a disordered system with hopping transport. This fact is fully supported by experimental results. The apparent MN energy was found to depend also on the shape of the DOS distribution and polaron binding energy.

Upon cooling a solution of poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene] (MEH-PPV), a phase transition occurs, leading to the formation of aggregates. We have studied the dynamics of singlet excitons in MEH-PPV solution below the critical temperature of the phase transition using steady-state photoluminescence measurements and pump–probe fs-spectroscopy at different temperatures. Spectral analysis indicates the coexistence of disordered chromophores with highly planarized chromophores. The high planarity is evidenced by a remarkably high 0–0/0–1 peak ratio in the spectra. By spectrally separating the contributions of either type of chromophore to the pump–probe signal we find that energy transfer takes place within less than 1 ps from disordered, unaggregated chain segments to highly planarized, aggregated chain segments. The short time scale of the energy transfer indicates intimate intermixing of the planarized and disordered polymeric chromophores.

In an endeavor to correlate the optoelectronic properties of π-conjugated polymers with their structural properties, we investigated the aggregation of P3HT in THF solution within a temperature range from 300 to 5 K. By detailed steady-state, site-selective, and time-resolved fluorescence spectroscopy combined with Franck–Condon analyses, we show that below a certain transition temperature (265 K) aggregates are formed that prevail in different polymorphs. At 5 K, we can spectroscopically identify two H-type aggregates with planar polymer backbones yet different degree of order regarding their side chains. Upon heating, the H-character of the aggregates becomes gradually eroded, until just below the transition temperature the prevailing “aggregate” structure is that of still phase-separated, yet disordered main and side chains. These conclusions are derived by analyzing the vibrational structure of the spectra and from comparing the solution spectra with those obtained from thin films that were cooled slowly from the melting temperature to room temperature and that had been analyzed previously by various X-ray techniques. In addition, site selectively recorded fluorescence spectra show that there is—dependent on temperature—energy transfer from higher energy to lower energy aggregates. This suggests that they must form clusters with dimensions of the exciton diffusion length, i.e., several nanometers in diameter.

This paper presents a detailed spectroscopic investigation of luminescence properties of 4,4′-bis(N-carbazolyl)-1,1′-biphenyl (CBP) and N,N,N′,N′-tetraphenylbenzidine (TAD) in solutions and neat films. These compounds are compared to their derivatives CDBP and TDAD that contain methyl groups in the 2 and 2′ position of the biphenyl core. We find that whereas steric twisting in CDBP and TDAD leads to a high triplet energy of about 3.0 and 3.1 eV, respectively, these compounds also tend to form triplet excimers in a neat film, in contrast to CBP and TAD. By comparison with N-phenylcarbazole (NPC) and triphenylamine (TPA), on which these compounds are based, as well as with the rigid spiro analogues to CBP and TAD we show that the reduced excimer formation in CBP and TAD can be attributed to a localization of the excitation onto the central biphenyl part of the molecule.

The field dependence of the photocurrent in a bilayer assembly is measured with the aim to clarify the role of excess photon energy in an organic solar cell comprising a polymeric donor and an acceptor. Upon optical excitation of the donor an electron is transferred to the acceptor forming a Coulomb-bound electron–hole pair. Since the subsequent escape is a field assisted process it follows that photogeneration saturates at higher electric fields, the saturation field being a measure of the separation of the electron–hole pair. Using the low bandgap polymers, PCDTBT and PCPDTBT, as donors and C60 as acceptor in a bilayer assembly it is found that the saturation field decreases when the photon energy is roughly 0.5 eV above the S1–S0 0–0 transition of the donor. This translates into an increase of the size of the electron-hole-pair up to about 13 nm which is close to the Coulomb capture radius. This increase correlates with the onset of higher electronic states that have a highly delocalized character, as confirmed by quantum-chemical calculations. This demonstrates that accessing higher electronic states does favor photogeneration yet excess vibrational energy plays no role. Experiments on intrinsic photogeneration in donor photodiodes without acceptors support this reasoning.

Charge separation at the donor–acceptor interface is a key step for high efficiency in organic solar cells. If interfacial hybrid states exist already in the dark it is plausible that they can have a major impact on the dissociation of optically generated excitations. In this work we probe such interfacial states via steady state absorption spectroscopy. A substantial bleaching of the absorption spectrum is found near the absorption edge when an electron-accepting layer of either trinitrofluorenone (TNF), C60, or a perylene-diimide derivative is deposited on top of a layer of electron-donating conjugated polymers, such as MEH-PPV or various poly-phenylene. This is in part attributed to the formation of ground state complexes with low oscillator strength. The experiments bear out a correlation between the reduction of the absorbance with the energy gap between the donor-HOMO and acceptor-LUMO, the effective conjugation length of the donor, and the efficiency of exciton dissociation in the solar cell. The effect originates from mixing of the donor-HOMO and the acceptor LUMO. Calculations using density functional theory support this reasoning. Implications for efficiency of organic solar cells will be discussed.

We developed an analytical model to describe hopping conductivity and mobility in organic semiconductors including both energetic disorder and polaronic contributions. The model is based on the Marcus jump rates with a Gaussian energetic disorder, and it is premised upon a generalized Effective Medium approach yet avoids shortcoming involved in the effective transport energy or percolation concepts. The carrier concentration dependence becomes considerably weaker when the polaron energy increases relative to the disorder energy, indicating the absence of universality that is at variance with recent publications.

Conjugated poly(3-hexylthiophene) (P3HT) chains are known to exist at least
in two distinct conformations: a coiled phase and a better ordered aggregated phase.
Employing steady state absorption and fluorescence spectroscopy, we measure the course of
aggregation of P3HT in tetrahydrofuran (THF) solution within a temperature range of 300 K
to 170 K. We show that aggregation is a temperature controlled process, driven by a
thermodynamic order−disorder transition. The transition temperature increases with the
molecular weight of the chains and can be rationalized in the theory of Sanchez. This implies
a smearing out of the phase transition in samples with increasing polydispersity and erodes
the signature of a first order phase transition. The detection of a hysteresis when undergoing
cooling/heating cycles further substantiates this reasoning.

The diffusion of fullerenes such as C 60 and PCBM in organic semiconductors
is a key factor in controlling the effi ciency of organic solar cells, though
it is challenging to measure and to control. A simple optical method based
on photoluminescence quenching is developed to assess the diffusion of
a quencher molecule such as C 60 through a semiconducting polymer fi lm,
in this case made with the polymer polyfl uorene. When the mobility of the
polymer chains is reduced by chemical crosslinking, the diffusion coeffi cient
of C 60 can be reduced by up to three orders of magnitude.

We synthesize a polytriphenylamine homopolymer and two donor–acceptor copolymers (D–A-copolymers) based on triphenylamine (TPA) as donor in combination with two different acceptor moieties to study the effect of the acceptor unit on the excited-state charge-transfer characteristics (CT-characteristics) and charge separation. The two acceptor moieties are a dicyanovinyl group in the side chain and a thieno[3,4-b]thiophene carboxylate in the main chain. Absorption and photoluminescence studies show new CT-bands for both of the D–A-copolymers. Field-dependent charge extraction studies in bilayer solar cells indicate a stronger CT-character for the copolymer in which the acceptor group is less conjugated with the copolymer backbone. The D–A-copolymer carrying the acceptor unit in the main chain exhibits smaller excitonic CT-character and good conjugation leading to less-bound electron–hole pairs and a better charge separation. This fundamental study gives insight into the interdependence of conjugation, charge carrier mobility, and solar cell performance for two different D–A-copolymers.

Imitating the natural “energy cascade” architecture, we present a single-molecular rod-like nano-light harvester (NLH) based on a cylindrical polymer brush. Block copolymer side chains carrying (9,9-diethylfl uoren-2-yl)methyl methacrylate units as light absorbing antennae (energy donors) are tethered to a linear polymer backbone containing 9-anthracenemethyl methacrylate units as emitting groups (energy acceptors). These NLHs exhibit very effi cient energy absorption and transfer. Moreover, we manipulate the energy transfer by tuning the donor–acceptor distance.

We present two classes of host materials for blue phosphors. The first are carbazole substituted biphenyls 1-9. In these CBP-type materials the triplets are confined to one half of the molecules by using either twisted biphenyls or by a metalinkage of the carbazoles to the biphenyl. We obtained high triplet energies of 2.95-2.98 eV and high glass transition temperatures in the range of 100-120 °C. OLEDs were fabricated using the host material 6 and the carbene emitter Ir(dbfmi) with pure blue emission at 450 nm. The devices achieved an external quantum efficiency of 8.7% at 100 cd/m2 and 6.1% at 1000 cd/m2. MBPTRZ with an electron transporting biscarbazolyltriazine that is separated from the hole transporting carbazole by a non-conjugated, meta-linked biphenyl unit is an example for a bipolar matrix material. The excellent glass forming properties and the high Tg of 132 °C ensure morphological stability in OLEDs. The meta-linkage and the additional twist at the biphenyl unit, which is achieved by two methyl groups in the 2- and 2’-position of the biphenyl in MBPTRZ leads to a decoupling of the electron accepting and electron donating part and therefore to a high triplet energy of 2.81 eV. DFT calculations show a clear separation of the electron and hole transporting moieties. A phosphorescent OLED with MBPTRZ as host and FIrpic as emitter reached a maximum external quantum efficiency of 7.0%, a current efficiency of 16.3 cd/A and a power efficiency of 6.3 lm/W.

Two novel bipolar host materials BPTRZ and MBPTRZ were synthesized, in which the hole transporting carbazole is separated from the electron transporting triazine moiety by a fully aromatic, but nonconjugated meta-linked biphenyl unit. The additional twist at the biphenyl in MBPTRZ, which is achieved by methyl-substitution in 2- and 2 ′ -position of the biphenyl leads to a higher triplet energy of 2.81 eV compared to 2.70 eV for BPTRZ. Both materials possess high thermal stabilities and good glass forming properties. An organic light emitting diode with MBPTRZ as host for the blue phosphorescence emitter FIrpic shows a maximum luminance of 30600 cd/m 2 and a maximum external quantum e ffi ciency of 7.0%.

The ratio of the 0-0 to 0-1 peak intensities in the photoluminescence (PL) spectrum of red-phase poly[2-methoxy-5-(2-ethylhexyloxy)-1,4-phenylenevinylene], better known as MEH-PPV, is significantly enhanced relative to the disordered blue-phase and is practically temperature independent in the range from T = 5 K to 180 K. The PL lifetime is similarly temperature independent. The measured trends are accounted for by modeling red-phase MEH-PPV as disordered π-stacks of elongated chains. Using the HJ-aggregate Hamiltonian expanded to include site disorder amongst electrons and holes, the absorption and PL spectra of cofacial MEH-PPV dimers are calculated. The PL 0-0/0-1 line strength ratio directly responds to the competition between intrachain interactions which promote J-aggregate-like behavior (enhanced PL ratio) and interchain interactions which promote H-aggregate-like behavior (attenuated PL ratio). In MEH-PPV aggregates, J-like behavior is favored by a relatively large intrachain exciton bandwidth – roughly an order of magnitude greater than the interchain bandwidth – and the presence of disorder. The latter is essential for allowing 0-0 emission at low temperatures, which is otherwise symmetry forbidden. For Gaussian disorder distributions consistent with the measured (inhomogeneous) line widths of the vibronic peaks in the absorption spectrum, calculations show that the 0-0 peak maintains its dominance over the 0-1 peak, with the PL ratio and radiative lifetime practically independent of temperature, in excellent agreement with experiment. Interestingly, interchain interactions lead only to about a 30% drop in the PL ratio, suggesting that the MEH-PPV π-stacks – and strongly disordered HJ-aggregates in general – can masquerade as single (elongated) chains. Our results may have important applications to other emissive conjugated polymers such as the β-phase of polyfluorenes.

We developed an analytical model to describe hopping transport in organic semiconductors including both
energetic disorder and polaronic contributions due to geometric relaxation. The model is based on a Marcus
jump rate in terms of the small-polaron concept with a Gaussian energetic disorder, and it is premised upon
a generalized effective medium approach yet avoids shortcomings involved in the effective transport energy
or percolation concepts. It is superior to our previous treatment [Phys. Rev. B 76, 045210 (2007)] since it is
applicable at arbitrary polaron activation energy Ea with respect to the energy disorder parameter σ. It can be
adapted to describe both charge-carrier mobility and triplet exciton diffusion. The model is compared with results
fromMonte Carlo simulations.We show (i) that the activation energy of the thermally activated hopping transport
can be decoupled into disorder and polaron contributions whose relative weight depend nonlinearly on the σ/Ea
ratio, and (ii) that the choice of the density of occupied and empty states considered in configurational averaging
has a profound effect on the results of calculations of theMarcus hopping transport. The σ/Ea ratio governs also
the carrier-concentration dependence of the charge-carrier mobility in the large-carrier-concentration transport
regime as realized in organic field-effect transistors. The carrier-concentration dependence becomes considerably
weaker when the polaron energy increases relative to the disorder energy, indicating the absence of universality.
This model bridges a gap between disorder and polaron hopping concepts.

The performance of opto-electronic devices built from low-molecular-weight dye molecules depends crucially on the stacking properties and the resulting coupling of the chromophoric systems. Herein we investigate the influence of H-bonding amide and bulky substituents on the π-stacking of pyrene-containing small molecules in dilute solution, as supramolecular aggregates, and in the solid state. A set of four pyrene derivatives was synthesized in which benzene or 4-tert-butyl benzene was linked to the pyrene unit either through an ester or an amide. All four molecules form supramolecular H-aggregates in THF solution at concentrations above 1×10−4 mol/l. These aggregates were transferred on a solid support and crystallized. We investigate: the excimer formation rates within supramolecular aggregates; the formation of H-bonds as well as the optical changes during the transition from the amorphous to the crystalline state; and the excimer to monomer fluorescence ratio in crystalline films at low temperatures. We reveal that in solution supramolecular aggregation depends predominantly on the pyrene chromophores. In the crystalline state, however, the pyrene stacking can be controlled gradually by H-bonding and steric effects. These results are further confirmed by molecular modeling. This work bears fundamental information for tailoring the solid state of functional optoelectronic materials.

In disordered organic semiconductors, excited states and charges move by hopping in an inhomogeneously broadened density of states, thereby relaxing energetically (“spectral diffusion”). At low temperatures, transport can become kinetically frustrated and consequently dispersive. Experimentally, this is observed predominantly for triplet excitations and charges, and has not been reported for singlet excitations. We have addressed the origin of this phenomenon by simulating the temperature dependent spectral diffusion using a lattice Monte Carlo approach with either Miller–Abrahams or Förster type transfer rates. Our simulations are in agreement with recent fluorescence and phosphorescence experimental results. We show that frustrated and thus dispersive diffusion appears when the number of available hopping sites is limited. This is frequently the case for triplets that transfer by a short-range interaction, yet may also occur for singlets in restricted geometries or dilute systems. Frustration is lifted when more hopping sites become available, e.g., for triplets as a result of an increased conjugation in some amorphous polymer films.

Efficient exciton dissociation at a donor-acceptor interface is the crucial, yet not fully understood, step for obtaining high efficiency organic solar cells. Recent theoretical work suggested an influence of polymer conjugation length and of interfacial dipoles on the exciton dissociation yield. This necessitates experimental verification. To this end, we measured the dissociation yield of several polymer/C60 planar heterojunction solar cells up to high electric fields. The results indeed prove that the yield of exciton dissociation depends strongly on the conjugation length of the polymers. Complementary photoemission experiments were carried out to assess the importance of dipoles at the donor-acceptor interfaces. Comparison of exciton dissociation models with experimental data shows that the widely used Onsager-Braun approach is unsuitable to explain photodissociation in polymer/C60 cells. Better agreement can be obtained using “effective mass” models that incorporate conjugation length effects by considering a reduced effective mass of the hole on the polymer and that include dielectric screening effects by interfacial dipoles. However, successful modeling of the photocurrent field dependence over a broad field range, in particular for less efficient solar cell compounds, requires that the dissociation at localized acceptor sites is also taken into account.

In order to unravel the intricate interplay between disorder effects, molecular reorganization, and charge carrier localization, a comprehensive study was conducted on hole transport in a series of conjugated alternating phenanthrene indenofluorene copolymers. Each polymer in the series contained one further comonomer comprising monoamines, diamines, or amine-free structures, whose influence on the electronic, optical, and charge transport properties was studied. The series covered a wide range of highest occupied molecular orbital (HOMO) energies as determined by cyclovoltammetry. The mobility, inferred from time-of-flight (ToF) experiments as a function of temperature and electric field, was found to depend exponentially on the HOMO energy. Since possible origins for this effect include energetic disorder, polaronic effects, and wave function localization, the relevant parameters were determined using a range of methods. Disorder and molecular reorganization were established first by an analysis of absorption and emission measurements and second by an analysis of the ToF measurements. In addition, density functional theory calculations were carried out to determine how localized or delocalized holes on a polymer chain are and to compare calculated reorganization energies with those that have been inferred from optical spectra. In summary, we conclude that molecular reorganization has little effect on the hole mobility in this system while both disorder effects and hole localization in systems with low-lying HOMOs are predominant. In particular, as the energetic disorder is comparable for the copolymers, the absolute value of the hole mobility at room temperature is determined by the hole localization associated with the triarylamine moieties.

In semiconducting polymers, the mobility of negative charges is typically much smaller than that of positive
charges. Identification of a universal electron-trap level that is associated with water complexation now clarifies
this difference and provides guidelines for the design of improved organic semiconductors.

We have investigated how electronic excitations that couple via short-range interaction, i.e., triplet excitations and charge carriers, move in a disordered organic semiconductor. In this systematic study, we paid special emphasis to the transition from quasi-equilibrium to nonequilibrium transport as the temperature is lowered from 300 to 10 K. As a method, we used Monte Carlo simulations employing both Marcus as well as Miller–Abrahams (MA) transition rates. The simulation parameters are the degree of static energetic disorder, the geometric reorganization energy, and the degree of electronic coupling among the hopping sites. In the case of conjugated polymers, the effects of intrachain versus interchain transport are taken into account. In the simulations, we monitor the spectral relaxation of excitations as well as their diffusivity. We find that, below a disorder controlled transition temperature, transport becomes kinetically frustrated and, concomitantly, dispersive. In this temperature regime, transport is controlled by single phonon tunneling, tractable in terms of MA rates, while in the high temperature regime multiphonon hopping, described by Marcus rates, prevails. The results also provide a quantitative assessment of dispersive excitation transport within the intermediate temperature regime in which no analytic theory is available so far. Quantitative agreement between simulation and previous experiments allows one to extract system parameters such as the minimum hopping time and to delineate the parameter range in which Marcus and MA rates should be used in transport studies.

We have investigated the electrical transport properties of poly(3,4-ethylenedioxythiophen)/poly(4-styrene-sulfonate) (PEDOT:PSS) with PEDOT-to-PSS ratios from 1:1 to 1:30. By combining impedance spectroscopy with thermoelectric measurements, we are able to independently determine the variation of electrical conductivity and charge carrier density with PSS content. We find the charge carrier density to be independent of the PSS content. Using a generalized effective media theory, we show that the electrical conductivity in PEDOT:PSS can be understood as percolation between sites of highly conducting PEDOT:PSS complexes with a conductivity of 2.3 (Xcm)
1 in a matrix of excess PSS with a low conductivity of 10
3 (X cm)
1. In addition to the transport properties, the thermoelectric power factors and Seebeck coefficients have been determined. VC 2012 Wiley Periodicals, Inc. J Polym Sci Part B: Polym Phys 50: 976–983, 2012

The poly(p-phenylene vinylene) derivative MEH-PPV is known to exist as two morphologically distinct species, referred to as red phase and blue phase. We show here that the transition from the blue phase to the red phase is a critical phenomenon that can be quantitatively described as a second order phase transition with a critical temperature Tc of 204 K. The criticality is associated with the trade-off between the gain in the electronic stabilization energy when the π- system of a planarized chain can delocalize and the concomitant loss of entropy. We studied this transition by measuring the absorption and fluorescence in methyltetrahydrofuran (MeTHF) in two different concentrations as a function of temperature. The spectra were analyzed based upon the Kuhn exciton model to extract effective conjugation lengths. At room temperature, the chains have effective conjugation lengths of about five repeat units in the ground state (the blue phase), consistent with a disordered defect cylinder conformation. Upon cooling below the critical temperature Tc, the red phase with increased effective conjugation lengths of about 10 repeat units forms, implying a more extended and better ordered conformation. Whereas aggregation is required for the creation of the red phase, its electronic states have a predominant intrachain character.

The intrinsic non-radiative decay (internal conversion) from the triplet excited state in phosphorescent dyes can be described by a multi-phonon emission process. Since non-radiative decay of triplet excitons can be a significant process in organic light-emitting diodes, a detailed understanding of this decay mechanism is important if the overall device efficiency is to be controlled. We compare a deuterated Pt(II)-containing phenylene ethynylene with its non-deuterated counterpart in order to investigate which phonon modes control to the non-radiative decay path. We observe that deuteration does not decrease the non-radiative decay rate. A Franck-Condon analysis of the phosphorescence spectra shows that the electronic excitation is coupled strongly to the breathing mode of the phenyl ring and the C≡C carbon stretching modes, while high-energy C-H or C-D stretching modes play an insignificant role. We, therefore, associate the internal conversion process with the carbon-carbon stretching vibrations.

Internal photocurrent quantum yields near 100% can be obtained from the separation of loosely bound geminate pairs when sufficiently large electric fields are applied to organic heterojunctions. The fields needed for complete electron–hole dissociation decrease to those prevailing in organic solar cells under operating conditions when well-conjugated polymers are employed.

Aggregate formation in poly(3-hexylthiophene) depends on molecular weight, solvent, and synthetic method. The interplay of these parameters thus largely controls device performance. In order to obtain a quantitative understanding on how these factors control the resulting electronic properties of P3HT, we measured absorption in solution and in thin films as well as the resulting field effect mobility in transistors. By a detailed analysis of the absorption spectra, we deduce the fraction of aggregates formed, the excitonic coupling within the aggregates, and the conjugation length within the aggregates, all as a function of solvent quality for molecular weights from 5 to 19 kDa. From this, we infer in which structure the aggregated chains pack. Although the 5 kDa samples form straight chains, the 11 and 19 kDa chains are kinked or folded, with conjugation lengths that increase as the solvent quality reduces. There is a maximum fraction of aggregated chains (about 55 ± 5%) that can be obtained, even for poor solvent quality. We show that inducing aggregation in solution leads to control of aggregate properties in thin films. As expected, the field-effect mobility correlates with the propensity to aggregation. Correspondingly, we find that a well-defined synthetic approach, tailored to give a narrow molecular weight distribution, is needed to obtain high field effect mobilities of up to 0.01 cm2/Vs for low molecular weight samples (=11 kDa), while the influence of synthetic method is negligible for samples of higher molecular weight, if low molecular weight fractions are removed by extraction.

Although carbazole-containing copolymers are frequently used as hole-transporting host materials for polymer organic light-emitting diodes (OLEDs), they often suffer from the formation of undesired exciplexes when the OLED is operated. The reason why exciplexes sometimes form for electrical excitation, yet not for optical excitation is not well understood. Here, we use luminescence measurements and quantum chemical calculations to investigate the mechanism of such exciplex formation for electrical excitation (electroplex formation) in a carbazole–pyridine copolymer. Our results suggest that the exciplex is formed via a positively charged interchain precursor complex. This complex is stabilized by interactions that involve the nitrogen lone pairs on both chain segments.

Despite the central role of light absorption and the subsequent generation of free charge carriers in organic and hybrid organic-inorganic photovoltaics, the precise process of this initial photoconversion is still debated. We employ a novel broadband (UV-Vis-NIR) transient absorption spectroscopy setup to probe charge generation and recombination in the thin films of the recently suggested hybrid material combination poly(3-hexylthiophene)/silicon (P3HT/Si) with 40 fs time resolution. Our approach allows for monitoring the time evolution of the relevant transient species under various excitation intensities and excitation wavelengths. Both in regioregular (RR) and regiorandom (RRa) P3HT, we observe an instant (<40 fs) creation of singlet-excitons, which subsequently dissociate to form polarons in 140 fs. The quantum yield of polaron formation through dissociation of delocalized excitons is significantly enhanced by adding Si as an electron acceptor, revealing ultrafast electron transfer from P3HT to Si. P3HT/Si films with aggregated RR-P3HT are found to provide free charge carriers in planar as well as in bulk heterojunctions and losses are due to nongeminate recombination. In contrast for RRa-P3HT/Si, geminate recombination of bound carriers is observed as the dominant loss mechanism. Site-selective excitation by variation of pump wavelength uncovers an energy transfer from P3HT coils to aggregates with a 1/e transfer time of 3 ps and reveals a factor of 2 more efficient polaron formation using aggregated RR-P3HT compared to disordered RRa-P3HT. Therefore, we find that polymer structural order rather than excess energy is the key criterion for free charge generation in hybrid P3HT/Si solar cells.

We have studied the temperature dependence of phosphorescence (Ph) and delayed fluorescence (DF) in two series of poly(p-phenylene) derivatives within a temperature range from 10 to 300 K under quasi-stationary conditions. One set of materials consists of the dimer, trimer, and polymer of ethylhexyl-substituted poly(fluorene) (PF2/6) and thus allows us to assess the effects of oligomer length. The second series addresses the influence of energetic disorder and conjugation length by being composed of the polymers alkoxy-substituted poly(p-phenylene) (DOO-PPP), poly(indenofluorene) (PIF), and ladder-type poly(p-phenylene) (MeLPPP). Under low light intensities, the DF features a maximum at a certain temperature Tmax. For the dimer and trimer, the Tmax coincides with the temperature at which the phosphorescence has decayed to 1/2 of the value at 10 K, while Tmax shifts to lower temperature values along the series DOO-PPP, PIF, and MeLPPP and approaches T = 0 K for MeLPPP. By applying conventional kinetic equations we show that the occurrence of a maximum in the DF intensity is the consequence of generalized thermally activated triplet exciton transport toward quenching sites. We find the quenching rates at 0 K to be in the range of 1 s–1 for the polymers, while they are more than an order of magnitude lower for the oligomers.

Organic semiconductor devices such as light-emitting diodes and solar cells frequently comprise a blend of molecular or polymeric materials. Consequently, resonant energy transfer between the components plays a major role in determining device performance. Energy transfer may take place through either single-step donor-acceptor transfer, realized for example as Forster transfer, or as a sequence of donor-donor transfers toward the acceptor site. Here we use a well-defined model system comprising an oligofluorene trimer, pentamer, or heptamer as the donor in combination with an anthracene derivative as the acceptor in order to study the rate and mechanism of energy transfer in thin films by time-resolved photoluminescence spectroscopy. We find the transfer process to be entirely dominated by sequential donor-donor transfer. In addition, we observe a strong dependence on oligomer length with an optimum energy transfer rate for the pentamer.

We report a series of CBP-derivatives with superior thermal and electronic properties for the use as host materials for blue electrophosphorescent organic light emitting diodes. We applied a systematic variation of the substitution pattern in the 2- and 2´-position of the biphenyl unit and the 3- and 6-position of the carbazole moieties. In contrast to the crystalline parent compound CBP, all methyl and trifluoromethyl substituted derivatives show amorphous behaviour. Substitution in the 2- and 2´-position of the biphenyl causes a twisting of the phenyl rings. Hence, the degree of conjugation of the molecules is limited which leads to enlarged triplet energies of approximately 2.95 eV compared to 2.58 eV for CBP. The methyl substitution at the active 3- and 6-position of the pendant carbazole units yields materials with an electrochemically stable behaviour against oxidation.

A series of trimethylsilyl-protected di-alkynes incorporating 3,4-ethylenedioxythiophene (EDOT) linker
groups Me3Si–C C–R–C C–SiMe3 (R = ethylenedioxythiophene-3,4-diyl 1a, 2,2¢-bis-3,4-
ethylenedioxythiophene-5,5¢-diyl 2a, 2,2¢,5¢,2¢¢-ter-3,4-ethylenedioxythiophene-5,5¢¢-diyl 3a) and the
corresponding terminal di-alkynes, H–C C–R–C C–H 1b–2b has been synthesized and characterized
and the single crystal X-ray structure of 1a has been determined. CuI-catalyzed dehydrohalogenation
reaction between trans-[(Ph)(Et3P)2PtCl] and the terminal di-alkynes 1b–2b in iPr2NH/CH2Cl2 (2 : 1
mole ratio) gives the Pt(II) di-ynes trans-[(Et3P)2(Ph)Pt–C C–R–C C–Pt(Ph)(Et3P)2] 1M–2M while
the dehydrohalogenation polycondensation reaction between trans-[(nBu3P)2PtCl2] and 1b–2b (1 : 1 mole
ratio) under similar reaction conditions affords the Pt(II) poly-ynes trans-[Pt(PnBu3)2–C C–R–C C-]n
1P–2P. The di-ynes and poly-ynes have been characterized spectroscopically and, for 1M and 2M, by
single-crystal X-ray which confirms the “rigid rod” di-yne backbone. The materials possess excellent
thermal stability, are soluble in common organic solvents and readily cast into thin films. Optical
absorption spectroscopic measurements reveal that the EDOT spacers create stronger donor-acceptor
interactions between the platinum(II) centres and conjugated ligands along the rigid backbone of the
organometallic polymers compared to the related non-fused and fused oligothiophene spacers.

Carbazole-based materials such as 4,4´-bis(N -carbazolyl)-2,2´-biphenyl (CBP) and its derivatives are frequently used as matrix materials for phosphorescent emitters in organic light emitting diodes (OLED)s. An essential requirement for such matrix materials is a high energy of their first triplet excited state. Here we present a detailed spectroscopic investigation supported by density functional theory (DFT) calculations on two series of CBP derivatives, where CH3 and CF3 substituents on the 2- and 2´-position of the biphenyl introduce strong torsion into the molecular structure. We find that the resulting poor coupling between the two halves of the molecules leads to an electronic structure similar to that of N -phenyl-3,6-dimethylcarbazole, with a high triplet-state energy of 2.95 eV. However, we also observe a triplet excimer emission centered at about 2.5-2.6 eV in all compounds. We associate this triplet excimer with a sandwich geometry of neighboring carbazole moieties. For compounds with the more polar CF3 substituents, the lifetime of the intermolecular triplet excited state extends into the millisecond range for neat films at room temperature. We attribute this to an increased charge-transfer character of the intermolecular excited state for the more polar substituents.

Dexter-type triplet transfer is a phenomenon that is ubiquitous in the field of molecular electronics, and that takes place at the interface of chemistry, physics and biology. It may be considered as a correlated transfer of two charges, and thus, models originally developed for charge transfer may be applied to describe triplet transfer. In dilute fluid solutions, triplet transfer from a donor to an acceptor is well-understood and it has been described in terms of Marcus theory, i.e. taking into account distortions in the molecule and its surroundings. In amorphous thin films, that are used for organic semiconductor applications, the effects of energetic disorder prevail, and they need to be considered for an appropriate description of triplet energy transfer. We present here an overview on recent experimental and theoretical work concerning a unified description of triplet energy transfer.

Energetic disorder is manifested in the inhomogeneous broadening of optical transitions in π-conjugated organic materials, and it is a key parameter that controls the dynamics of charge and energy transfer in this promising class of amorphous semiconductors. In an endeavor to understand which processes cause the inhomogeneous broadening of singlet and triplet excitations in π-conjugated polymers we analyze continuous wave absorption and photoluminescence spectra within a broad range of temperatures for (i) oligomers of the phenylenevinylene family (OPVs) and MEH-PPV in solution and (ii) bulk films of MEH-PPV and members of the poly(p-phenylene) family (PPPs). We use a Franck-Condon deconvolution technique to determine the temperature dependent S1-S0 0-0 and T1-S0 0-0 transition energies and their related variances. For planar compounds, the transition energies can be related to the oligomer length, which allows us to infer the effective conjugation length for the nonplanar compounds as a function of temperature. With this information we can distinguish between intrachain contributions to the inhomogeneous line broadening that are due to thermally induced torsional displacements of the chain elements, and other contributions that are assigned largely to dielectric interactions between the chain and its environment. We find that in solution, temperature-induced torsional displacements dominate the line broadening for the alkyl derivatives of OPVs while in the alkoxy derivatives the Van der Waals contribution prevails. In films, σ is virtually temperature independent because disorder is frozen in. We also establish a criterion regarding the ratio of inhomogeneous line broadening in singlet and triplet states. The results will be compared to a recent theory by Barford and Trembath.

The synthesis and characterization of the thieno[3,2-b]thiophene and dithieno[3,2-b:2′,3′-d]thiophene containing platinum(II) poly-ynes and their molecular precursors is described and the electronic structure is established by absorption, luminescence and photoinduced absorption measurements. A comparison of the electronic structure of the fused and the nonfused oligothiophenes, thieno[3,2-b]thiophene, dithieno[3,2-b:2′,3′-d]thiophene, 2,2′-bithiophene, and 2,2′:5′,2” -terthiophene incorporated in platinum(II) poly-ynes is reported. We find the singlet S1 and triplet T1 and Tn excited states to be at higher energy in thin films made from the fused systems than from the nonfused systems. For ligands with the same number of rings, we attribute this to the decreased number of double bonds in the fused system and to the presence of an additional sulfur atom in spacers with the same number of double bonds.

Abstract: The nature of Dexter triplet energy transfer between bonded systems of a red phosphorescent iridium complex 13 and a conjugated polymer, polyfluorene, has been investigated in electrophosphorescent organic light-emitting diodes. Red-emitting phosphorescent iridium complexes based on the [Ir(btp)2(acac)] fragment (where btp is 2-(2¢-benzo[b]thienyl)pyridinato and acac is acetylacetonate) have been attached either directly (spacerless) or through a -(CH2)8- chain (octamethylene-tethered) at the 9-position of a 9-octylfluorene host. The resulting dibromo-functionalized spacerless (8) or octamethylene-tethered (12) fluorene monomers were chain extended by Suzuki polycondensations using the bis(boronate)-terminated fluorene macromonomers 16 in the presence of end-capping chlorobenzene solvent to produce the statistical spacerless (17) and octamethylene-tethered (18) copolymers containing an even dispersion of the pendant phosphorescent fragments. The spacerless monomer 12 adopts a face-to-face conformation with a separation of only 3.6 Å between the iridium complex and fluorenyl group, as shown by X-ray analysis of a single crystal, and this facilitates intramolecular triplet energy transfer in the spacerless copolymers 17. The photo- and electroluminescence efficiencies of the octamethylene-tethered copolymers 18 are double those of the spacerless copolymers 17, and this is consistent with suppression of the back transfer of triplets from the red phosphorescent iridium complex to the polyfluorene backbone in 18. The incorporation of a -(CH2)8- chain between the polymer host and phosphorescent guest is thus an important design principle for achieving higher efficiencies in those electrophosphorescent organic light-emitting diodes for which the triplet energy levels of the host and guest are similar.

The photo- and electroluminescence properties of a series of novel, heteroleptic, mer-cyclometallated iridiumcomplexes have been fine-tuned from green to blue by changing the substituents on the pyridyl ring of the phenylpyridyl ligand. The X-ray crystal structures of two Ir-based triazolyl complexes are reported.

We report the synthesis and photophysical study of a series of solution-processible phosphorescent iridium complexes. These comprise bis-cyclometalated iridium units [Ir(ppy)2(acac)] or [Ir(btp)2(acac)] where ppy is 2-phenylpyridinato, btp is 2-(2‘-benzo[b]thienyl)pyridinato, and acac is acetylacetonate. The iridium units are covalently attached to and in conjugation with oligo(9,9-dioctylfluorenyl-2,7-diyl) [(FO)n] to form complexes [Ir(ppy-(FO)n)2(acac)] or [Ir(btp-(FO)n)2(acac)], where the number of fluorene units, n, is 1, 2, 3, 10, 20, 30, or 40. All the complexes exhibit emission from a mixed triplet state in both photoluminescence and electroluminescence, with efficient quenching of the fluorene singlet emission. Short-chain complexes, 11-13, [Ir(ppy-(FO)n-FH)2(acac)] where n = 0, 1, or 2, show green light emission, red-shifted through the FO attachment by about 70 meV, but for longer chains there is quenching because of the lower energy triplet state associated with polyfluorene. In contrast, polymer complexes 18-21 [Ir(btp-(FO)n)2(acac)] where n is 5-40 have better triplet energy level matching and can be used to provide efficient red phosphorescent polymer light-emitting diodes, with a red shift due to the fluorene attachment of about 50 meV. We contrast this small (50-70 meV) and short-range modification of the triplet energies through extended conjugation, with the much more substantial evolution of the p-p* singlet transitions, which saturate at about n = 10. These covalently bound materials show improvements in efficiency over simple blends and will form the basis of future investigations into energy-transfer processes occurring in light-emitting diodes.