| Literature DB >> 28295734 |
Fuwen Zhao1,2, Shuixing Dai1,3, Yang Wu4, Qianqian Zhang5, Jiayu Wang1, Li Jiang2, Qidan Ling3, Zhixiang Wei6, Wei Ma4, Wei You5, Chunru Wang2, Xiaowei Zhan1.
Abstract
A new fluorinated nonfullerene acceptor, ITIC-Th1, has been designed and synthesized by introducing fluorine (F) atoms onto the end-capping group 1,1-dicyanomethylene-3-indanone (IC). On the one hand, incorporation of F would improve intramolecular interaction, enhance the push-pull effect between the donor unit indacenodithieno[3,2-b]thiophene and the acceptor unit IC due to electron-withdrawing effect of F, and finally adjust energy levels and reduce bandgap, which is beneficial to light harvesting and enhancing short-circuit current density (JSC ). On the other hand, incorporation of F would improve intermolecular interactions through CF···S, CF···H, and CF···π noncovalent interactions and enhance electron mobility, which is beneficial to enhancing JSC and fill factor. Indeed, the results show that fluorinated ITIC-Th1 exhibits redshifted absorption, smaller optical bandgap, and higher electron mobility than the nonfluorinated ITIC-Th. Furthermore, nonfullerene organic solar cells (OSCs) based on fluorinated ITIC-Th1 electron acceptor and a wide-bandgap polymer donor FTAZ based on benzodithiophene and benzotriazole exhibit power conversion efficiency (PCE) as high as 12.1%, significantly higher than that of nonfluorinated ITIC-Th (8.88%). The PCE of 12.1% is the highest in fullerene and nonfullerene-based single-junction binary-blend OSCs. Moreover, the OSCs based on FTAZ:ITIC-Th1 show much better efficiency and better stability than the control devices based on FTAZ:PC71 BM (PCE = 5.22%).Entities:
Keywords: fluorination; fused-ring electron acceptors; nonfullerene; polymer solar cells
Year: 2017 PMID: 28295734 DOI: 10.1002/adma.201700144
Source DB: PubMed Journal: Adv Mater ISSN: 0935-9648 Impact factor: 30.849