Side-chain engineering for efficient non-fullerene polymer solar cells based on a wide-bandgap polymer donor

被引:65
|
作者
Fan, Qunping [1 ]
Su, Wenyan [1 ]
Guo, Xia [1 ]
Wang, Yan [1 ]
Chen, Juan [1 ]
Ye, Chennan [1 ]
Zhang, Maojie [1 ]
Li, Yongfang [1 ,2 ]
机构
[1] Soochow Univ, Coll Chem Chem Engn & Mat Sci, State & Local Joint Engn Lab Novel Funct Polymer, Lab Adv Optoelect Mat, Suzhou 215123, Peoples R China
[2] Chinese Acad Sci, CAS Key Lab Organ Solids, Inst Chem, Beijing Natl Lab Mol Sci, Beijing 100190, Peoples R China
基金
中国国家自然科学基金;
关键词
POWER CONVERSION EFFICIENCY; ENERGY-LEVEL MODULATION; PHOTOVOLTAIC PERFORMANCE; CONJUGATED POLYMER; 2D-CONJUGATED POLYMER; ACCEPTOR; BENZODITHIOPHENE; COPOLYMERS; TERPOLYMERS; ALKYLTHIO;
D O I
10.1039/c7ta02075a
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
In this work, a new wide-bandgap polymer, PSBZ, based on thienyl substituted benzodithiophene (BDTT) as the donor unit and difluorobenzotriazole (BTz-2F) as the acceptor unit was synthesized for photovoltaic applications. Compared to the analogous polymer J61 with linear dodecylthio side chains in the BDTT unit and a long 2-hexyldecyl side chain in BTz-2F, PSBZ possesses branched 2-butyloctyl side chains to increase steric hindrance of the BDTT unit and a short 2-butyloctyl side chain to decrease steric hindrance of the BTz-2F unit for more efficient charge separation and transport in the devices. As a result, PSBZ exhibited stronger pi-pi interaction and smaller stacking spacing leading to a higher extinction coefficient of 1.48 x 10(5) cm(-1) and a high hole mobility of 8.56 x 10(-3) cm(2) V-1 s(-1). Compared to the analogous polymer J61 with a power conversion efficiency (PCE) of 9.53% and a short-circuit current density (J(sc)) of 17.43 mA cm(-2), the PSBZ: ITIC-based polymer solar cells yielded a higher PCE of 10.5% with a higher J(sc) of 19.0 mA cm(-2). The results show that our design strategy is successful for improving photovoltaic performance by side chain engineering.
引用
收藏
页码:9204 / 9209
页数:6
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