堆积
烷基
部分
有机太阳能电池
材料科学
富勒烯
串联
位阻效应
纳米技术
高分子化学
化学工程
化学
有机化学
聚合物
复合材料
工程类
作者
Chenyu Han,Bowen Cheng,Zhen Fu,Hao Wang,Shengqi Ji,Jingnan Wu,Sixuan Cheng,Xinxin Xia,Hang Yin,Xiaoyan Du,Ergang Wang,Xia Guo,Xiaotao Hao,Yongfang Li,Mao‐Jie Zhang
标识
DOI:10.1002/anie.202501592
摘要
Developing efficient and stable as‐cast organic solar cells (OSCs) is imperative for alleviating costs and complexity for large‐scale commercial applications. Nevertheless, achieving the desired double‐fibril morphology of active layer through single‐step processing is challenging. Herein, two non‐fullerene acceptors, namely BTP‐N6 and BTP‐V6, are designed and synthesized to construct as‐cast OSCs by introducing linear alkyl chains adjacent to the pyrrole moiety. The reduction of steric hindrance attributable to linear chains engenders diminished dihedral angles of molecular skeletons, thereby promoting compact and face‐on oriented molecular stacking. Moreover, BTP‐V6 featuring vinyl‐functionalized linear chains manifests additional interaction sites with neighboring molecules to instigate enhanced π‐π stacking during rapid film‐formation process, and engenders the formation of a refined double‐fibril network morphology, which facilitates exciton dissociation, bolsters charge carrier transport, and suppresses recombination loss. Consequently, the D18:BTP‐V6 based device attained a record‐shattering efficiency of 19.2% with a high fill factor (FF) of 80.7%, and also demonstrated robust thermal and shelf stability. Moreover, the meticulously optimized layer‐by‐layer (LBL) structured devices achieved an excellent efficiency up to 20.1%. This study introduces a viable strategy for alkyl chain modification to fabricate efficient and stable as‐cast devices, with the anticipation of expediting the progression toward widespread commercialization of OSCs.
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