分子间力
结晶度
材料科学
有机太阳能电池
接受者
三元运算
光伏系统
化学物理
异构化
分子
聚合物
有机化学
化学
计算机科学
物理
生态学
生物
复合材料
催化作用
程序设计语言
凝聚态物理
作者
Chenyu Han,Jianxiao Wang,Shuai Zhang,Liangliang Chen,Fuzhen Bi,Junjie Wang,Chunming Yang,Pengchao Wang,Yonghai Li,Xichang Bao
标识
DOI:10.1002/adma.202208986
摘要
Research on organic solar cells (OSCs) has progressed through material innovation and device engineering. However, well-known and ubiquitous intermolecular interactions, and particularly their synergistic effects, have received little attention. Herein, the complicated relationship between photovoltaic conversion and multidimensional intermolecular interactions in the active layers is investigated. These interactions are dually regulated by side-chain isomerization and end-cap engineering of the acceptors. The phenylalkyl featured acceptors (LA-series) exhibit stronger crystallinity with preferential face-on interactions relative to the alkylphenyl attached isomers (ITIC-series). In addition, the PM6 and LA-series acceptors exhibit moderate donor/acceptor interactions compared to those of the strongly interacting PM6/ITIC-series pairs, which helps to enhance phase separation and charge transport. Consequently, the output efficiencies of all LA series acceptors are over 14%. Moreover, LA-series acceptors show appropriate compatibility, host/guest interactions, and crystallinity relationships with BTP-eC9, thereby leading to uniform and well-organized "alloy-like" mixed phases. In particular, the highly crystalline LA23 further optimizes multiple interactions and ternary microstructures, which results in a high efficiency of 19.12%. Thus, these results highlight the importance of multidimensional intermolecular interactions in the photovoltaic performance of OSCs.
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