TY - JOUR
T1 - Side-Chain Engineering of Benzodithiophene-Fluorinated Quinoxaline Low-Band-Gap Co-polymers for High-Performance Polymer Solar Cells
AU - Xu, Xiaopeng
AU - Wu, Yulei
AU - Fang, Junfeng
AU - Li, Zuojia
AU - Wang, Zhenguo
AU - Li, Ying
AU - Peng, Qiang
N1 - Publisher Copyright:
© 2014 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.
PY - 2014/10/1
Y1 - 2014/10/1
N2 - A new series of donor-acceptor co-polymers based on benzodithiophene and quinoxaline with various side chains have been developed for polymer solar cells. The effect of the degree of branching and dimensionality of the side chains were systematically investigated on the thermal stability, optical absorption, energy levels, molecular packing, and photovoltaic performance of the resulting co-polymers. The results indicated that the linear and 2D conjugated side chains improved the thermal stabilities and optical absorptions. The introduction of alkylthienyl side chains could efficiently lower the energy levels compared with the alkoxyl-substituted analogues, and the branched alkoxyl side chains could deepen the HOMO levels relative to the linear alkoxyl chains. The branched alkoxyl groups induced better lamellar-like ordering, but poorer face-to-face packing behavior. The 2D conjugated side chains had a negative influence on the crystalline properties of the co-polymers. The performance of the devices indicated that the branched alkoxyl side chains improved the Voc, but decreased the Jsc and fill factor (FF). However, the 2D conjugated side chains would increase the Voc, Jsc, and FF simultaneously. For the first time, our work provides insight into molecular design strategies through side-chain engineering to achieve efficient polymer solar cells by considering both the degree of branching and dimensionality.
AB - A new series of donor-acceptor co-polymers based on benzodithiophene and quinoxaline with various side chains have been developed for polymer solar cells. The effect of the degree of branching and dimensionality of the side chains were systematically investigated on the thermal stability, optical absorption, energy levels, molecular packing, and photovoltaic performance of the resulting co-polymers. The results indicated that the linear and 2D conjugated side chains improved the thermal stabilities and optical absorptions. The introduction of alkylthienyl side chains could efficiently lower the energy levels compared with the alkoxyl-substituted analogues, and the branched alkoxyl side chains could deepen the HOMO levels relative to the linear alkoxyl chains. The branched alkoxyl groups induced better lamellar-like ordering, but poorer face-to-face packing behavior. The 2D conjugated side chains had a negative influence on the crystalline properties of the co-polymers. The performance of the devices indicated that the branched alkoxyl side chains improved the Voc, but decreased the Jsc and fill factor (FF). However, the 2D conjugated side chains would increase the Voc, Jsc, and FF simultaneously. For the first time, our work provides insight into molecular design strategies through side-chain engineering to achieve efficient polymer solar cells by considering both the degree of branching and dimensionality.
KW - conjugation
KW - donor-acceptor systems
KW - electrochemistry
KW - polymers
KW - solar cells
UR - https://www.scopus.com/pages/publications/84941054869
U2 - 10.1002/chem.201403153
DO - 10.1002/chem.201403153
M3 - 文章
AN - SCOPUS:84941054869
SN - 0947-6539
VL - 20
SP - 13259
EP - 13271
JO - Chemistry - A European Journal
JF - Chemistry - A European Journal
IS - 41
ER -