Electron Acceptors Based on α-Substituted Perylene Diimide (PDI) for Organic Solar Cells

被引:204
|
作者
Zhao, Donglin [1 ,2 ]
Wu, Qinghe [1 ,2 ]
Cai, Zhengxu [1 ,2 ]
Zheng, Tianyue [1 ,2 ]
Chen, Wei [3 ,4 ]
Lu, Jessica [1 ,2 ]
Yu, Luping [1 ,2 ]
机构
[1] Univ Chicago, Dept Chem, 929 East 57th St, Chicago, IL 60637 USA
[2] Univ Chicago, James Franck Inst, 929 East 57th St, Chicago, IL 60637 USA
[3] Argonne Natl Lab, Div Mat Sci, 9700 Cass Ave, Lemont, IL 60439 USA
[4] Univ Chicago, Inst Mol Engn, 5747 South Ellis Ave, Chicago, IL 60637 USA
基金
美国国家科学基金会;
关键词
POWER CONVERSION EFFICIENCY; NONFULLERENE ACCEPTORS; PYRENE DERIVATIVES; SMALL-MOLECULE; DONOR; GENERATION; FULLERENES; TRANSPORT; SINGLET; DESIGN;
D O I
10.1021/acs.chemmater.5b04570
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Perylene diimide (PDI) derivatives functionalized at the ortho-position (alpha PPID, alpha PBDT) were synthesized and used as electron acceptors in non-fullerene organic photovoltaic cells. Because of the good planarity and strong pi-stacking of ortho-functionalized PDI, the alpha PPID and alpha PBDT exhibit a strong tendency to form aggregates, which endow the materials with high electron mobility. The inverted OPVs employing alpha PDI-based compounds as the acceptors and PBT7-Th as the donor give the highest power conversion efficiency (PCE) values: 4.92% for alpha PBDT-based devices and 3.61% for alpha PPID-based devices, which are, respectively, 39% and 4% higher than that of their beta-substituted counterparts beta PBDT and beta PPID. Charge separation studies show more efficient exciton dissociation at interfaces between alpha PDI-based compounds and PTB7-Th. The results suggest that alpha-substituted PDI derivatives are more promising electron acceptors for organic photovoltaic (OPV) components than beta-isomers.
引用
收藏
页码:1139 / 1146
页数:8
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