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在非富勒烯供体-受体PTB7:PDI界面处的超快通道I和通道II电荷产生过程对其优异的光伏性能至关重要。

Ultrafast channel I and channel II charge generation processes at a nonfullerene donor-acceptor PTB7:PDI interface is crucial for its excellent photovoltaic performance.

作者信息

Li Kai, Xu Dong-Hui, Wang Xin, Liu Xiang-Yang

机构信息

College of Chemistry and Material Science, Sichuan Normal University, Chengdu 610068, China.

出版信息

Phys Chem Chem Phys. 2021 Jan 28;23(3):2097-2104. doi: 10.1039/d0cp05362g.

Abstract

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.

摘要

近年来,非富勒烯有机太阳能电池因其低成本、高吸收系数和出色的合成灵活性而备受关注。然而,相应的供体-受体界面处的微观光致动力学仍不清楚。在这项工作中,我们首先采用基于最先进的含时密度泛函理论(TDDFT)的非绝热动力学模拟,并结合静态电子结构计算,使用最小模型系统(172个原子)来探索典型的非富勒烯供体-受体PTB7:PDI界面处的超快光致动力学。用特定波长的光激发后,由于PTB7和PDI具有高吸收能力且吸收光谱有显著重叠,它们都可以被局部激发以产生|PTB7和|PDI激子。此后,这些局域激子逐渐转化为电荷转移激子|PTB7+PDI-,而另一种|PTB7-PDI+电荷转移激子不参与整个过程。随着激子的转化,电子从PTB7转移到PDI(通道I电荷产生)和空穴从PDI转移到PTB7(通道II电荷产生)同时发生,时间常数分别为643飞秒和549飞秒。与此同时,测量电子和空穴质心距离的D指数从1.0 Å增加到4.0 Å,这清楚地反映了界面处的电荷转移过程。我们目前的工作提供了确凿的证据,表明通道I和通道II电荷产生过程在PTB7:PDI界面都起着重要作用,这可能有助于设计具有更好光伏性能的新型非富勒烯太阳能电池。

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