有机太阳能电池
分子间力
接受者
烷基
材料科学
侧链
相(物质)
Crystal(编程语言)
结晶学
高分子化学
化学工程
分子
化学
有机化学
聚合物
复合材料
计算机科学
物理
工程类
程序设计语言
凝聚态物理
作者
Xin Zhao,Qiaoshi An,Heng Zhang,Can Yang,Asif Mahmood,Mengyun Jiang,Min Hun Jee,Bin Fu,Shiyu Tian,Han Young Woo,Yapei Wang,Jin‐Liang Wang
标识
DOI:10.1002/anie.202216340
摘要
Side-chain tailoring is a promising method to optimize the performance of organic solar cells (OSCs). However, asymmetric alkyl chain-based small molecular acceptors (SMAs) are still difficult to afford. Herein, we adopted a novel asymmetric n-nonyl/undecyl substitution strategy and synthesized two A-D1 A'D2 -A double asymmetric isomeric SMAs with asymmetric selenophene-based central core for OSCs. Crystallographic analysis indicates that AYT9Se11-Cl forms a more compact and order intermolecular packing compared to AYT11Se9-Cl, which contributed to higher electron mobility in neat AYT9Se11-Cl film. Moreover, the PM6 : AYT9Se11-Cl blend film shows a better morphology with appropriate phase separation and distinct face-on orientation than PM6 : AYT11Se9-Cl. The OSCs with PM6 : AYT9Se11-Cl obtain a superior PCE of 18.12 % compared to PM6 : AYT11Se9-Cl (17.52 %), which is the best efficiency for the selenium-incorporated SMAs in binary BHJ OSCs. Our findings elucidate that the promising double asymmetric strategy with isomeric alkyl chains precisely modulates the crystal packing and enhances the photovoltaic efficiency of selenophene-incorporated SMAs.
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