Bifunctional Bis-benzophenone as A Solid Additive for Non-Fullerene Solar Cells

被引:19
|
作者
Fan, Pu [1 ,2 ]
Sun, Wenjian [3 ]
Zhang, Xiaohua [1 ]
Wu, Yao [2 ]
Hu, Qin [2 ,4 ,5 ]
Zhang, Qing [3 ]
Yu, Junsheng [1 ]
Russell, Thomas P. [2 ,5 ]
机构
[1] Univ Elect Sci & Technol China UESTC, Sch Optoelect Sci & Engn, State Key Lab Elect Thin Films & Integrated Devic, Chengdu 610054, Peoples R China
[2] Univ Massachusetts, Polymer Sci & Engn Dept, 120 Governors Dr, Amherst, MA 01003 USA
[3] Shanghai Jiao Tong Univ, Sch Chem & Chem Engn, Dept Polymer Sci & Engn, Shanghai Key Lab Elect Insulat & Thermal Aging, Shanghai 200240, Peoples R China
[4] Univ Sci & Technol China, Sch Microelect, Hefei 230026, Anhui, Peoples R China
[5] Lawrence Berkeley Natl Lab, Mat Sci Div, Berkeley, CA 94720 USA
基金
中国国家自然科学基金;
关键词
non‐ fullerene solar cell; solid additive; thermal stability; thickness insensitivity; POLYMER; EFFICIENCY; TRANSPORT; ACCEPTOR; FILM;
D O I
10.1002/adfm.202008699
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Simultaneously improving efficiency and stability is critical for the commercial application of non-fullerene acceptor polymer solar cells (NFA-PSCs). Multifunctional solid additives have been considered as a potential route to tune the morphology of the active layer and optimize performance. In this work, photoinitiator bifunctional bis-benzophenone (BP-BP) is used as a solid additive, replacing solvent additives, in the PBDB-T:ITIC NFA system. With the addition of BP-BP, the intermolecular pi-pi stacking of PBDB-T and morphology is improved, leading to more balanced carrier transport and more effective exciton dissociation. Devices fabricated with BP-BP show a power conversion efficiency (PCE) of 11.89%, with enhanced short-circuit current (J(sc)), and fill factor (FF). Devices optimized with BP-BP show excellent reproducibility, insensitivity to thickness, and an improved thermal stability under atmospheric conditions without encapsulation. This work provides a new strategy for the application of solid additives in NFA-PSCs.
引用
收藏
页数:7
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