Interfacial Charge Transfer States Research Articles

On the role of asymmetric molecular geometry in high-performance organic solar cells

Although asymmetric molecular design has been widely demonstrated effective for organic photovoltaics (OPVs), the correlation between asymmetric molecular geometry and their optoelectronic properties is still unclear. To access this issue, we have designed and synthesized several symmetric-asymmetric non-fullerene acceptors (NFAs) pairs with identical physical and optoelectronic properties. Interestingly, we found that the asymmetric NFAs universally exhibited increased open-circuit voltage compared to their symmetric counterparts, due to the reduced non-radiative charge recombination. From our molecular-dynamic simulations, the asymmetric NFA naturally exhibits more diverse molecular interaction patterns at the donor (D):acceptor (A) interface as compared to the symmetric ones, as well as higher D:A interfacial charge-transfer state energy. Moreover, it is observed that the asymmetric structure can effectively suppress triplet state formation. These advantages enable a best efficiency of 18.80%, which is one of the champion results among binary OPVs. Therefore, this work unambiguously demonstrates the unique advantage of asymmetric molecular geometry, unveils the underlying mechanism, and highlights the manipulation of D:A interface as an important consideration for future molecular design.

Energetic inversion of singlet/triplet interfacial charge-transfer states for reduced energy loss in organic solar cells

Significant CT inversion can be achieved via hybridization of the triplet CT state with high-lying local triplet states, which benefits to concurrently reduce the triplet recombination and driving force for higher-efficiency organic photovoltaics.

(Invited) Interface Engineering for Organic and Perovskite Photovoltaics

Organic and perovskite solar cells have been intensively studied because they are considered as one of the most promising photovoltaic devices. Indeed, power conversion efficiencies (PCEs) have recently exceeded 19% for organic solar cells and 25% for perovskite solar cells. In both devices, interface engineering is highly important for efficient photovoltaic performance. In particular, it has great impact on open-circuit voltage (V OC) because charge carriers would recombine bimolecularly at the interface. In this talk, I will discuss how interface impact on V OC in polymer solar cells and perovskite solar cells.First, I will discuss how interfacial charge transfer (CT) states impact on V OC in polymer solar cells. More specifically, we employed two crystalline polymers (PTzBT-BOHD and PTzBT-12OD) and a fullerene derivative (PCBM). PTzBT-BOHD and PTzBT-12OD consist of the same backbone with different side chains: PTzBT-BOHD has two branched side chains of butyloctyl (BO) and hexyldecyl (HD) groups and PTzBT-12OD has a linear side chain of dodecyl (12) group and a branched side chain of octadecyl (OD) group. Interestingly, these PTzBT-BOHD/PCBM and PTzBT-12OD/PCBM solar cells exhibited different V OCs, although the two crystalline polymer neat films exhibit the same ionization energy because of the same backbone structure. In order to address the origin of the different V OCs, we carefully analyzed the interfacial CT state in the blend films. As a result, we found the interfacial CT state energy is higher in PTzBT-BOHD/PCBM than in PTzBT-12OD/PCBM blend films. This is because HOMO level of PTzBT-BOHD is deeper than that of PTzBT-12OD in disordered mixed phase in blend films, which results from twisted backbone of PTzBT-BOHD with branched side chains [1].Next, I will discuss how aging and passivation impact on interfacial energy matching and hence V OC in perovskite solar cells. As reported previously, V OC is often improved by ambient storage, which is called aging effect, and also improved by addition of passivation layers, which is called passivation effect. Such improvements in V OC suggest recombination would be suppressed effectively in these devices. Interestingly, V OC was gradually improved during ambient storage even for the passivated device where surface recombination is effectively suppressed by the passivation layer. By analyzing electronic properties of each layer, we found that no change was observed for the perovskite layer but the HOMO level deepening was observed for a hole-transporting material of spiro-OMeTAD during the ambient storage. As a result, energy matching between perovskite and spiro-OMeTAD layers was significantly improved and hence surface recombination was further effectively suppressed, resulting in the improvement in V OC [2,3].These findings clearly show that the electronic state at the interface critically impacts on V OC not only in polymer solar cells but also in perovskite solar cells, and therefore suggest that device design based on interface engineering is of particular importance for further improvement in V OC.

Room-temperature organic magnetoresistance based on interfacial ground charge transfer state

We propose an organic magnetoresistance (OMR) based on the weak interfacial ground charge transfer (IGCT) state at m-MTDATA/Alq3 heterojunction. The maximum OMR reaches 13.2% at room temperature under an external magnetic field of 300 mT, which is well interpreted by the different roles of singlet and triplet IGCT states in hole transport. As demonstrated, the hole transport is blocked by singlet IGCT and passed through by triplet IGCT. By manipulating the Larmor frequencies of mixing singlet and triplet IGCT states through Δg mechanism under an external magnetic field, the hole current is modulated, thus generating OMR. Furthermore, OMR can be further enhanced to 15.4% at 300 mT and 27.9% at 1000 mT by inserting a thin BCP interlayer between m-MTDATA and Alq3 layers. This picture will help to implement a giant OMR with interfacial CT states in the future.

Adsorption Structures Affecting the Electronic Properties and Photoinduced Charge Transfer at Perylene-Based Molecular Interfaces.

Perylene-based organic semiconductors are widely used in organic electronic devices. Here, we studied the ultrafast excited state dynamics after optical excitation at interfaces between the electron donor (D) diindenoperylene (DIP) and the electron acceptor (A) dicyano-perylene-bis(dicarboximide) (PDIR-CN2 ) using femtosecond time-resolved second harmonic generation (SHG) in combination with large scale quantum chemical calculations. Thereby, we varied in bilayer structures of DIP and PDIR-CN2 the interfacial molecular geometry. For an interfacial configuration which contains a edge-on geometry but also additional face-on domains an optically induced charge transfer (CT) is observed, which leads to a pronounced increase of the SHG signal intensity due to electric field induced second harmonic generation. The interfacial CT state decays within 7.5±0.7 ps, while the creation of hot CT states leads to a faster decay (5.3±0.2 ps). For the bilayer structures with mainly edge-on geometries interfacial CT formation is suppressed since π-π overlap perpendicular to the interface is missing. Our combined experimental and theoretical study provides important insights into D/A charge transfer properties, which is needed for the understanding of the interfacial photophysics of these molecules.

Elucidation of Active Sites and Mechanistic Pathways of a Heteropolyacid/Cu-Metal–Organic Framework Catalyst for Selective Oxidation of 5-Hydroxymethylfurfural via Ex Situ X-ray Absorption Spectroscopy and In Situ Attenuated Total Reflection-Infrared Studies

Chemoselective oxidation of 5-hydroxymethylfurfural (HMF) over non-noble metals to produce a bioplastic monomer, 2,5-furandicarboxylic acid (FDCA), under alkaline-free conditions is challenging and worthy of investigation. HMF oxidation into FDCA involves the concurrent oxidation of primary alcohol and an aldehyde functional group into carboxylic groups, which therefore demand a bifunctional catalyst containing dual active sites and chemoselective oxidation of HMF. The present work demonstrated the formation of new selective active sites in a composite porous material (Cu-BTC_PMA) that consists of Cu-BTC (metal–organic framework (MOF)) and polyoxometalate (POM). The porous framework provides (Cu-BTC_PMA) the desired chemoselectivity, while a selective Cu metal center in Cu-BTC (MOF) and Cu–O–Mo sites functions as active sites for the concurrent oxidation of HMF into FDCA. This catalyst exhibited a HMF conversion of 89% and an FDCA selectivity of 92.3% under base-free and mild reaction conditions. In detail, X-ray absorption spectroscopy analysis demonstrated the chemical bond tuning, as well as electronic structural modulations of MOF and POM at the molecular level, which directs the formation of new synergistic interfacial active sites and charge transfer states. This phenomenon causes the generation of the unique redox environment of copper and the multiple oxidation states along with the oxygen vacancy in the Cu-BTC_PMA catalyst, which most likely behaves as active sites for base-free oxidation. A kinetics study of this reaction was followed using in situ attenuated total reflection-infrared spectroscopy, demonstrating the stabilization of the specific intermediates that lead to the formation of FDCA. Moreover, we made comparative density functional theory and quantum theory of atoms in molecules investigations on the surface interaction between the reactant (HMF) and two catalyst models of Cu-BTC and Cu-BTC_PMA to interpret quantitatively the higher catalytic activity of the Cu-BTC_PMA catalyst. The kinetics study also evaluates the rate-determining step and activation energy for the multistep oxidation reactions.

Atomic-scale insights into the interfacial charge transfer in a NiO/CeO2 heterostructure for electrocatalytic hydrogen evolution

To understand the underlying mechanism of the interfacial charge transfer and local chemical state variation in the nonprecious-based hydrogen evolution reaction (HER) electrocatalysts, a model system of the NiO/CeO2 heterostructure was chosen for investigation using a combination of the advanced electron microscopic characterization and first-principles calculations. The results directly proved that interfacial charge transfer occurs from Ni to Ce, leading to reduction in the valence state of Ce and increased formation of VO. This would optimize ΔGH* and facilitate the hydrogen evolution process, resulting in outstanding HER performance in 1 M KOH with a low overpotential of 99 mV at the current density of 10 mA•cm−2 and a modest Tafel slope of 78.4 mV•dec−1 for the NiO/CeO2 heterostructure sample. Therefore, the improved HER performance could be attributed to the synergistic coupling interactions and electron redistribution at the interface of NiO and CeO2. These results concretely demonstrate the direct determination of the interfacial structure of the heterostructure and provide atomistic insights to unravel the underlying mechanism of interfacial charge transfer induced HER performance improvement.

Interplay between charge separation and hole back transfer determines the efficiency of non-fullerene organic solar cells with low energy level offset

Organic bulk heterojunction solar cells with electron acceptors based on small donor-acceptor type molecules show record efficiencies mainly due to their long wavelength absorption, which enables efficient harvesting of solar light and, thus, causes high current density. Meanwhile, relative positions of HOMO and LUMO levels of donor and acceptor materials determine the open circuit voltage. Here, we apply ultrafast transient absorption and transient luminescence techniques together with specially-designed modelling technique to address charge carrier generation and recombination dynamics in detail. We demonstrate the importance of careful adjustment of the HOMO and LUMO levels, as their positions determine formation and recombination rates of interfacial charge transfer (CT) states. An insufficient donor and acceptor LUMO level offset, lower than ∼300 meV, leads to slow and inefficient CT state formation, while an offset of the HOMO level below ∼100 meV leads to fast CT state recombination, which we attribute to the back transfer of a hole from the donor to the acceptor. • CT state formation was investigated by ultrafast transient techniques and modelling. • ∼300 meV LUMO offset is required for efficient CT state generation. • > 100 meV HOMO offset is sufficient for ultrafast hole transfer. • Low HOMO offset opens a loss channel via the back transfer of an electron.

(Invited) Discovering Bottlenecks and Opportunities in Hybrid Solar Light Harvesting Systems By Ultrafast X-Ray Spectroscopy

A prerequisite for advancing hybrid solar light harvesting systems is a comprehensive understanding of photoinduced electronic dynamics across a wide range of spatial and temporal scales. Time-resolved spectroscopy techniques in the optical domain have proven instrumental in identifying critical timescales of fundamental processes, such as interfacial charge transfer, charge migration, and carrier lifetimes, which are intimately linked to a system's performance. New light source and instrument developments open opportunities to extend such studies into the X-ray regime. Due to their inherent elemental specificity and sensitivity to local electronic environments, time-domain X-ray spectroscopy techniques are uniquely suited to gain a microscopic picture of dynamics from well-defined reporter sites within often complex nanoscale light harvesting architectures. We will present new insights into fundamental photoinduced dynamics in several archetypical heterostructures based on femtosecond and picosecond time-resolved X-ray photoemission spectroscopy (TRXPS).The photoinduced transient charge redistribution in the model hybrid system of nanoporous zinc oxide (ZnO) sensitized by ruthenium bipyridyl chromophores is probed independently from the viewpoints of the molecular electron donor and the semiconductor acceptor.[1] Charge injection from the chromophore into the semiconductor is found to proceed via a transiently populated interfacial charge transfer (ICT) complex on an overall timescale of ~300 ps. Our results show that, even after release from the ICT states into the ZnO conduction band, the injected electrons remain localized within less than 6 nm from the interface, due to enhanced downward band-bending by the photo-injected charge carriers. This spatial confinement suggests that light-induced charge generation and transport in nanoscale ZnO photocatalytic devices proceeds predominantly within the defect-rich surface region, which may lead to enhanced surface recombination and explain their lower performance compared to titanium dioxide (TiO2)-based systems. The quantitative nature and surface sensitivity of TRXPS also provides direct access to the spatial separation of the holes remaining on the bipyridyl chromophores after charge injection from the semiconductor surface with sub-nm precision.Complementary femtosecond and picosecond TRXPS studies of photoinduced dynamics in copper-phthalocyanine(CuPc)-C60 heterojunctions provide a deeper understanding of both exciton migration pathways toward the interface as well as the absolute efficiency by which ICT states dissociate into separate charges.[2] The measurements reveal surprisingly efficient charge generation from triplet excitons and from the lowest lying ICT states, both of which were previously believed to be inactive during light-to-charge conversion.Photoinduced charge transfer dynamics between spherical gold nanoparticles (AuNPs) and a nanoporous film of TiO2 is monitored by picosecond TRXPS, providing direct access to the absolute photon-to-charge conversion efficiency and subsequent electron-hole recombination dynamics.[3] Preliminary results will be presented for the extension of the measurements into the ambient pressure regime, taking a first step toward the study of photoinduced interfacial chemistry by TRXPS in this model system for nanoplasmonic light harvesting applications.[1] S. Neppl et al., “Nanoscale Confinement of Photo-Injected Electrons at Hybrid Interfaces”, J. Phys. Chem. Lett. 12, 11951 (2021).[2] F. Roth et al., “Direct observation of charge separation in an organic light harvesting system by femtosecond time-resolved XPS”, Nat. Commun. 12, 1196 (2021).[3] M. Borgwardt et al., “Photoinduced Charge Carrier Dynamics and Electron Injection Efficiencies in Au Nanoparticle-Sensitized TiO2 Determined with Picosecond Time-Resolved X-ray Photoelectron Spectroscopy”, J. Phys. Chem. Lett. 11, 5476 (2020). Figure 1

Thermally Activated Reverse Electron Transfer Limits Carrier Generation Efficiency in PM6:Y6 Non‐Fullerene Organic Solar Cells

Transient absorption and time‐resolved fluorescence measurements in a wide temperature range are used to investigate the mechanism of charge carrier generation in efficient organic solar cells based on a PM6:Y6 donor–acceptor blend. The generation mechanisms differ significantly under excitation of a donor or acceptor. The investigations reveal a temperature‐dependent interplay between the formation of interfacial charge transfer (CT) states and intra‐moiety CT states of the acceptor, their separation into free charge carriers and carrier recombination. The efficient charge carrier generation is ensured by the carrier separation over a small energy barrier, which is easily surmountable at room temperature. However, the overall yield of charge carrier generation at room temperature is reduced by the recombination of charge carriers due to the thermally activated back transfer of electrons from the acceptor to the donor via the highest occupied molecular orbit (HOMO) levels, which is enabled by the small energy offset between HOMO levels of the donor and the acceptor.

Efficient Interfacial Upconversion Enabling Bright Emission at an Extremely Low Driving Voltage in Organic Light‐Emitting Diodes (Advanced Optical Materials 4/2022)

In article number 2101710, Seiichiro Izawa, Masahiro Morimoto, Shigeki Naka, and Masahiro Hiramoto report an efficient organic light-emitting diode (OLED), operable by a 1.5-V battery, that produces bright emission equivalent to the luminance of a typical display. The OLED is based on an upconversion transition through triplet–triplet annihilation near its donor/acceptor interface. The efficient upconversion is realized by controlling the character of an interfacial charge transfer state, which is a key intermediate.

Charge transfer state characterization and voltage losses of organic solar cells

A correct determination of voltage losses is crucial for the development of organic solar cells (OSCs) with improved performance. This requires an in-depth understanding of the properties of interfacial charge transfer (CT) states, which not only set the upper limit for the open-circuit voltage of a system, but also govern radiative and non-radiative recombination processes. Over the last decade, different approaches have emerged to classify voltage losses in OSCs that rely on a generic detailed balance approach or additionally include CT state parameters that are specific to OSCs. In the latter case, a correct determination of CT state properties is paramount. In this work, we summarize the different frameworks used today to calculate voltage losses and provide an in-depth discussion of the currently most important models used to characterize CT state properties from absorption and emission data of organic thin films and solar cells. We also address practical concerns during the data recording, analysis, and fitting process. Departing from the classical two-state Marcus theory approach, we discuss the importance of quantized molecular vibrations and energetic hybridization effects in organic donor-acceptor systems with the goal to providing the reader with a detailed understanding of when each model is most appropriate.

Theoretical Study of Non-Fullerene Acceptors Using End-Capped Groups with Different Electron-Withdrawing Abilities toward Efficient Organic Solar Cells.

Acceptors in organic solar cells (OSCs) are of paramount importance. On the basis of the well-known non-fullerene acceptor Y6, six acceptors (Y6-COH, Y6-COOH, Y6-CN, Y6-SO2H, Y6-CF3, and Y6-NO2) were designed by end-capped manipulation. The effects of end-capped engineering on electronic properties, optical properties, and interfacial charge-transfer states were systematically studied by density functional theory, time-dependent density functional theory, and molecular dynamics. The designed acceptors possess suitable energy levels and improved optical properties. More importantly, the electron mobility of the new acceptors was greatly enhanced, even more than 20 times that of the parent molecule. Among them, Y6-NO2 with the lowest-lying frontier molecular orbitals and the largest red-shifted absorption was selected to construct interfaces with the donor PM6. PM6/Y6-NO2 exhibits stronger interfacial interactions and enhanced charge-transfer characteristics compared with PM6/Y6. This work not only enhances the understanding of the structure-property relationship for acceptors but also offers a set of promising acceptors for high-performance OSCs.

Short Excited-State Lifetimes Mediate Charge-Recombination Losses in Organic Solar Cell Blends with Low Charge-Transfer Driving Force.

A blend of a low-optical-gap diketopyrrolopyrrole polymer and a fullerene derivative, with near-zero driving force for electron transfer, is investigated. Using femtosecond transient absorption and electroabsorption spectroscopy, the charge transfer (CT) and recombination dynamics as well as the early-time transport are quantified. Electron transfer is ultrafast, consistent with a Marcus-Levich-Jortner description. However, significant charge recombination and unusually short excited (S1 ) and CT state lifetimes (≈14ps) are observed. At low S1 -CT offset, a short S1 lifetime mediates charge recombination because: i) back-transfer from the CT to the S1 state followed by S1 recombination occurs and ii) additional S1 -CT hybridization decreases the CT lifetime. Both effects are confirmed by density functional theory calculations. In addition, relatively slow (tens of picoseconds) dissociation of charges from the CT state is observed, due to low local charge mobility. Simulations using a four-state kinetic model entailing the effects of energetic disorder reveal that the free charge yield can be increased from the observed 12% to 60% by increasing the S1 and CT lifetimes to 150ps. Alternatively, decreasing the interfacial CT state disorder while increasing bulk disorder of free charges enhances the yield to 65% in spite of the short lifetimes.

Adjusting the energy of interfacial states in organic photovoltaics for maximum efficiency

A critical bottleneck for improving the performance of organic solar cells (OSC) is minimising non-radiative losses in the interfacial charge-transfer (CT) state via the formation of hybrid energetic states. This requires small energetic offsets often detrimental for high external quantum efficiency (EQE). Here, we obtain OSC with both non-radiative voltage losses (0.24 V) and photocurrent losses (EQE > 80%) simultaneously minimised. The interfacial CT states separate into free carriers with ≈40-ps time constant. We combine device and spectroscopic data to model the thermodynamics of charge separation and extraction, revealing that the relatively high performance of the devices arises from an optimal adjustment of the CT state energy, which determines how the available overall driving force is efficiently used to maximize both exciton splitting and charge separation. The model proposed is universal for donor:acceptor (D:A) with low driving forces and predicts which D:A will benefit from a morphology optimization for highly efficient OSC.

Identifying the Molecular Origins of High-Performance in Organic Photodetectors Based on Highly Intermixed Bulk Heterojunction Blends

A bulk-heterojunction (BHJ) structure of organic semiconductor blend is widely used in photon-to-electron converting devices such as organic photodetectors (OPD) and photovoltaics (OPV). However, the impact of the molecular structure on the interfacial electronic states and optoelectronic properties of the constituent organic semiconductors is still unclear, limiting further development of these devices for commercialization. Herein, the critical role of donor molecular structure on OPD performance is identified in highly intermixed BHJ blends containing a small-molecule donor and C60 acceptor. Blending introduces a twisted structure in the donor molecule and a strong coupling between donor and acceptor molecules. This results in ultrafast exciton separation (<1 ps), producing bound (binding energy ∼135 meV), localized (∼0.9 nm), and highly emissive interfacial charge transfer (CT) states. These interfacial CT states undergo efficient dissociation under an applied electric field, leading to highly efficient OPDs in reverse bias but poor OPVs. Further structural twisting and molecular-scale aggregation of the donor molecules occur in blends upon thermal annealing just above the transition temperature of 150 °C at which donor molecules start to reorganize themselves without any apparent macroscopic phase-segregation. These subtle structural changes lead to significant improvements in charge transport and OPD performance, yielding ultralow dark currents (∼10-10 A cm-2), 2-fold faster charge extraction (in μs), and nearly an order of magnitude increase in effective carrier mobility. Our results provide molecular insights into high-performance OPDs by identifying the role of subtle molecular structural changes on device performance and highlight key differences in the design of BHJ blends for OPD and OPV devices.

Spatial Anisotropy of Charge Transfer at Perfluoropentacene-Pentacene (001) Single-Crystal Interfaces and its Relevance for Thin Film Devices.

Archetypal donor-acceptor (D-A) interfaces composed of perfluoropentacene (PFP) and pentacene (PEN) are examined for charge transfer (CT) state formation and energetics as a function of their respective molecular configuration. To exclude morphological interference, our structural as well as highly sensitive differential reflectance spectroscopy studies were carried out on PFP thin films epitaxially grown on PEN(001) single-crystal facets. Whereas the experimental data supported by complementary theoretical calculations confirm the formation of a strong CT state in the case of a cofacial PFP-PEN stacking, CT formation is energetically less favorable and thus absent for the corresponding head-to-tail configuration as disclosed for the first time. In view of technological implementations, the knowledge gained on the single-crystal references is transferred to thin-film diodes composed of either stacked PFP/PEN bilayers or mixed PFP:PEN heterojunction interfaces. As demonstrated, their electronic and electroluminescent behavior can be consistently described by the absence or presence of interfacial CT states. Thus, our results hint at the thorough design of D-A interfaces to achieve the highest device performances.

Long-lived and disorder-free charge transfer states enable endothermic charge separation in efficient non-fullerene organic solar cells

Organic solar cells based on non-fullerene acceptors can show high charge generation yields despite near-zero donor–acceptor energy offsets to drive charge separation and overcome the mutual Coulomb attraction between electron and hole. Here, we use time-resolved optical spectroscopy to show that free charges in these systems are generated by thermally activated dissociation of interfacial charge-transfer states that occurs over hundreds of picoseconds at room temperature, three orders of magnitude slower than comparable fullerene-based systems. Upon free electron–hole encounters at later times, both charge-transfer states and emissive excitons are regenerated, thus setting up an equilibrium between excitons, charge-transfer states and free charges. Our results suggest that the formation of long-lived and disorder-free charge-transfer states in these systems enables them to operate closely to quasi-thermodynamic conditions with no requirement for energy offsets to drive interfacial charge separation and achieve suppressed non-radiative recombination.

Exciton and Charge Carrier Dynamics in Highly Crystalline PTQ10:IDIC Organic Solar Cells

AbstractHerein the morphology and exciton/charge carrier dynamics in bulk heterojunctions (BHJs) of the donor polymer PTQ10 and molecular acceptor IDIC are investigated. PTQ10:IDIC BHJs are shown to be particularly promising for low cost organic solar cells (OSCs). It is found that both PTQ10 and IDIC show remarkably high crystallinity in optimized BHJs, with GIWAXS data indicating pi‐pi stacking coherence lengths of up to 8 nm. Exciton‐exciton annihilation studies indicate long exciton diffusion lengths for both neat materials (19 nm for PTQ10 and 9.5 nm for IDIC), enabling efficient exciton separation with half lives of 1 and 3 ps, despite the high degree of phase segregation in this blend. Transient absorption data indicate exciton separation leads to the formation of two spectrally distinct species, assigned to interfacial charge transfer (CT) states and separated charges. CT state decay is correlated with the appearance of additional separate charges, indicating relatively efficient CT state dissociation, attributed to the high crystallinity of this blend. The results emphasize the potential for high material crystallinity to enhance charge separation and collection in OSCs, but also that long exciton diffusion lengths are likely to be essential for efficient exciton separation in such high crystallinity devices.

Charge Separation from an Intra-Moiety Intermediate State in the High-Performance PM6:Y6 Organic Photovoltaic Blend.

Bulk-heterojunction organic photovoltaic devices with nonfullerene acceptors (NFAs) exhibit efficient hole transfer with small interfacial energy offset, which results in power conversion efficiencies above 17% in single junction devices using the high-performance NFA of Y6. However, the underlying mechanism responsible for the hole transfer channel in the polymer/Y6 blends remains poorly understood. Herein, we report that the hole transfer channel of photocharge generation is mediated by an intra-moiety excited state in a blend of donor polymer PM6 and NFA Y6 using broadband transient absorption (TA) spectroscopy. By comparing the TA data recorded from the solution and film Y6 samples, we identify the ultrafast formation of an intra-moiety excimer state together with the conversion from the primary local excitation on a time scale of ∼0.2 ps in the Y6 film. The intra-moiety excimer state acts as the intermediate for the hole transfer channel, which dissociates into free polarons on a time scale of ∼15 ps in the PM6/Y6 blend at room temperature. The intra-moiety intermediate state, arising from the intermolecular coupling in Y6 domains, is markedly different from the interfacial charge transfer state, which is commonly accepted as the intermediate state for the electron transfer channel. These findings suggest that manipulating the interplay between intra-moiety and interfacial excited species can provide a promising route for further improving device performance.