材料科学
噻吩
聚合物
连接器
堆积
接受者
聚合物太阳能电池
结晶学
高分子化学
有机化学
化学
复合材料
凝聚态物理
计算机科学
操作系统
物理
作者
Han Yu,Yan Wang,Ha Kyung Kim,Xin Wu,Yuhao Li,Ze‐Fan Yao,Mingao Pan,Xinhui Zou,Jianquan Zhang,Shangshang Chen,Dahui Zhao,Fei Huang,Xinhui Lu,Zonglong Zhu,He Yan
标识
DOI:10.1002/adma.202200361
摘要
State-of-art Y-series polymer acceptors are typically based on a mono-thiophene linker, which can cause some twisted molecular conformations and thus limit the performance of all-polymer solar cells (all-PSCs). Here, a high-performance polymer acceptor based on vinylene linkers is reported, which leads to surprising changes in the polymers' molecular conformations, optoelectronic properties, and enhanced photovoltaic performance. It is found that the polymer acceptors based on thiophene or bithiophene linkers (PY-T-γ and PY-2T-γ) display significant molecular twisting between end-groups and linker units, while the vinylene-based polymer (PY-V-γ) exhibits a more coplanar and rigid molecular conformation. As a result, PY-V-γ demonstrates a better conjugation and tighter interchain stacking, which results in higher mobility and a reduced energetic disorder. Furthermore, detailed morphology investigations reveal that the PY-V-γ-based blend exhibits high domain purity and thus a better fill factor in its all-PSCs. With these, a higher efficiency of 17.1% is achieved in PY-V-γ-based all-PSCs, which is the highest efficiency reported for binary all-PSCs to date. This work demonstrates that the vinylene-linker is a superior unit to build polymer acceptors with more coplanar and rigid chain conformation, which is beneficial for polymer aggregation and efficient all-PSCs.
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