Non-fullerene acceptors with hetero-dihalogenated terminals induce significant difference in single crystallography and enable binary organic solar cells with 17.5% efficiency

被引:143
作者
Wang, Lai [1 ]
An, Qiaoshi [1 ]
Yan, Lu [1 ]
Bai, Hai-Rui [1 ]
Jiang, Mengyun [1 ]
Mahmood, Asif [1 ]
Yang, Can [1 ]
Zhi, Hongfu [1 ]
Wang, Jin-Liang [1 ]
机构
[1] Beijing Inst Technol, Beijing Key Lab Photoelect Electrophoton Convers, Key Lab Cluster Sci, Sch Chem & Chem Engn,Minist Educ, Beijing 100081, Peoples R China
关键词
END-GROUP; PERFORMANCE; MORPHOLOGY; BULK;
D O I
10.1039/d1ee01832a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Despite the dihalogenation of terminals being an effective strategy to produce efficient nonfullerene acceptor (NFA)-based organic solar cells (OSCs), hetero-dihalogenated terminals are quite difficult to prepare. Here, we synthesized, for the first time, two new hetero-dihalogenated terminals (FCl-IC and FBr-IC) with a fluorine/chlorine or fluorine/bromine pair at one terminal and three NFAs (Y-BO-FCl, Y-BO-FBr, and Y-BO-ClBr) with three hetero-dihalogenated terminals (FCl-IC, FBr-IC, and ClBr-IC) using a general process for OSCs, respectively. A neat film of Y-BO-FCl presents a slightly lower energy level in comparison to those of Y-BO-FBr and Y-BO-ClBr. We, for the first time, obtained single crystals of hetero-dihalogenated NFAs. On going from Y-BO-ClBr single crystals to fluorinated acceptor single crystals, the crystal systems and intermolecular packing motifs were significantly improved. The crystallographic and theoretical analysis indicate that Y-BO-FCl exhibits the most planar molecular geometry, the shortest intermolecular packing distance and Largest pi-pi electronic coupling among these acceptors. Moreover, PM6:Y-BO-FCl blend films present more ordered face-on orientation crystallinity, more suitable fiber-Like phase separation, higher and more balanced charge mobility, and weaker charge recombination in comparison with those of PM6:Y-BO-FBr and PM6:Y-BO-ClBr. As a result, a performance of up to a remarkable power conversion efficiency of 17.52% with an enhanced FF value of ca. 78% was achieved in binary Y-BO-FCl: PM6 devices compared to those of PM6:Y-BO-FBr (16.47%) and PM6:Y-BO-ClBr (13.61%), which to date is the highest efficiency for a hetero-halogenated NFAs-based OSC. Our investigations demonstrate that a fluorine/chlorine hetero-dihalogenated terminal represents a new and effective synergistic strategy to induce significant differences in single crystals and produce high-performance hetero-halogenated NFA-based OSCs.
引用
收藏
页码:320 / 333
页数:14
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