苝
二亚胺
电子受体
有机太阳能电池
电子
光化学
材料科学
化学
化学工程
有机化学
分子
物理
聚合物
工程类
量子力学
作者
Dong-Lin Zhao,Qinghe Wu,Zhengxu Cai,Tianyue Zheng,Wei Chen,Jessica R. Lu,Luping Yu
标识
DOI:10.1021/acs.chemmater.5b04570
摘要
Perylene diimide (PDI) derivatives functionalized at the ortho-position (αPPID, αPBDT) were synthesized and used as electron acceptors in non-fullerene organic photovoltaic cells. Because of the good planarity and strong π-stacking of ortho-functionalized PDI, the αPPID and αPBDT exhibit a strong tendency to form aggregates, which endow the materials with high electron mobility. The inverted OPVs employing αPDI-based compounds as the acceptors and PBT7-Th as the donor give the highest power conversion efficiency (PCE) values: 4.92% for αPBDT-based devices and 3.61% for αPPID-based devices, which are, respectively, 39% and 4% higher than that of their β-substituted counterparts βPBDT and βPPID. Charge separation studies show more efficient exciton dissociation at interfaces between αPDI-based compounds and PTB7-Th. The results suggest that α-substituted PDI derivatives are more promising electron acceptors for organic photovoltaic (OPV) components than β-isomers.
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