Low-bandgap non-fullerene acceptors based on selenophene π spacer and alkylated indaceno[1,2-b:5,6-b'] dithiophene for organic solar cells

被引:12
|
作者
Zhang, Xiaowei [1 ]
Wang, Qi [1 ]
Liang, Ziqi [1 ]
Li, Miaomiao [1 ]
Geng, Yanhou [1 ,2 ]
机构
[1] Tianjin Univ, Sch Mat Sci & Engn, Tianjin 300072, Peoples R China
[2] Tianjin Univ, Collaborat Innovat Ctr Chem Sci & Engn Tianjin, Tianjin Key Lab Mol Optoelect Sci, Tianjin 300072, Peoples R China
基金
中国国家自然科学基金;
关键词
Organic solar cells; Non-fullerene acceptors; Low bandgap; Alkyl side chains; Selenophene pi spacer; NONACYCLIC ELECTRON-ACCEPTORS; ENERGY-LEVEL MODULATION; SMALL-MOLECULE ACCEPTOR; EFFICIENT; ACHIEVE;
D O I
10.1016/j.orgel.2019.03.038
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Three non-fullerene acceptors, i.e. IDT2SeC2C4, IDT2SeC2C4-2F and IDT2SeC2C4-4F, with selenophene pi bridge between central alkylated indaceno[1,2-b: 5,6-b'] dithiophene (IDT) unit and terminal 1,1-dicyano-methylene-3-indanones (ICs) with 0-2 fluorine substituents were synthesized. These molecules presented low optical band gaps in the range of 1.30-1.44 eV. Moreover, compared with the counterparts with phenyl side chains on IDT unit, the alkyl-based molecules achieved higher electron mobility owing to the more ordered and closer p-p stacking. Organic solar cells (OSCs) based on the non-fullerene acceptors were fabricated with the wide band gap polymer PBDB-T as donor. Attributed to the desired morphology with more obvious fibril-like structures, the devices based on IDT2SeC2C4-2F and IDT2SeC2C4-4F with fluorinated IC terminals delivered high power conversion efficiencies (PCEs) over 10%, whereas the devices based on DT2SeC2C4 showed a lower PCE of 8.92%.
引用
收藏
页码:200 / 207
页数:8
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