TY - JOUR
T1 - Electron Acceptors Based on α-Substituted Perylene Diimide (PDI) for Organic Solar Cells
AU - Zhao, Donglin
AU - Wu, Qinghe
AU - Cai, Zhengxu
AU - Zheng, Tianyue
AU - Chen, Wei
AU - Lu, Jessica
AU - Yu, Luping
N1 - Publisher Copyright:
© 2016 American Chemical Society.
PY - 2016/2/23
Y1 - 2016/2/23
N2 - 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. (Graph Presented).
AB - 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. (Graph Presented).
UR - http://www.scopus.com/inward/record.url?scp=84958963172&partnerID=8YFLogxK
U2 - 10.1021/acs.chemmater.5b04570
DO - 10.1021/acs.chemmater.5b04570
M3 - Article
AN - SCOPUS:84958963172
SN - 0897-4756
VL - 28
SP - 1139
EP - 1146
JO - Chemistry of Materials
JF - Chemistry of Materials
IS - 4
ER -