Ultrafast channel I and channel II charge generation processes at a nonfullerene donor–acceptor PTB7:PDI interface is crucial for its excellent photovoltaic performance
Literature Information
Kai Li, Dong-Hui Xu, Xin Wang, Xiang-Yang Liu
Nonfullerene organic solar cells have received much attention in recent years due to their low cost, high absorption coefficient and excellent synthetic flexibility. However, the microscopic photoinduced dynamics at corresponding donor–acceptor interfaces remains unclear. In this work, we have firstly employed state-of-the-art TDDFT-based nonadiabatic dynamics simulations in combination with static electronic structure calculations to explore the ultrafast photoinduced dynamics at a typical nonfullerene donor–acceptor PTB7:PDI interface using a minimal model system (172 atoms). Upon excitation with specific wavelength of light, both PTB7 and PDI can be locally excited to generate |PTB7*〉 and |PDI*〉 excitons due to their high absorption ability and significant overlap in absorption spectrum. After that, these localized excitons gradually convert to charge transfer exciton |PTB7+PDI−〉, while another |PTB7−PDI+〉 charge transfer exciton is not involved in the whole process. Along with the exciton conversion, electron transfer from PTB7 to PDI (channel I charge generation) and the hole transfer from PDI to PTB7 (channel II charge generation) occurs simultaneously with time constants of 643 fs and 549 fs respectively. In the same time, D index that measures the centroid distance of electron and hole increases from 1.0 Å to 4.0 Å, which clearly reflects a charge transfer process at the interface. Our present work provides solid evidence that both channel I and channel II charge generation processes play important roles at PTB7:PDI interface, which could be helpful for the design of novel nonfullerene solar cells with better photovoltaic performance.
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Physical Chemistry Chemical Physics (PCCP) is an international journal co-owned by 19 physical chemistry and physics societies from around the world. This journal publishes original, cutting-edge research in physical chemistry, chemical physics and biophysical chemistry. To be suitable for publication in PCCP, articles must include significant innovation and/or insight into physical chemistry; this is the most important criterion that reviewers and Editors will judge against when evaluating submissions. The journal has a broad scope and welcomes contributions spanning experiment, theory, computation and data science. Topical coverage includes spectroscopy, dynamics, kinetics, statistical mechanics, thermodynamics, electrochemistry, catalysis, surface science, quantum mechanics, quantum computing and machine learning. Interdisciplinary research areas such as polymers and soft matter, materials, nanoscience, energy, surfaces/interfaces, and biophysical chemistry are welcomed if they demonstrate significant innovation and/or insight into physical chemistry. Joined experimental/theoretical studies are particularly appreciated when complementary and based on up-to-date approaches.











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