Conjugated polymer acceptors based on fused perylene bisimides with a twisted backbone for non-fullerene solar cells

被引:43
|
作者
Jiang, Xudong [1 ,2 ]
Xu, Yunhua [1 ]
Wang, Xiaohui [3 ]
Yang, Fan [2 ]
Zhang, Andong [2 ]
Li, Cheng [2 ]
Ma, Wei [3 ]
Li, Weiwei [2 ]
机构
[1] Beijing Jiaotong Univ, Sch Sci, Dept Chem, Beijing 100044, Peoples R China
[2] Chinese Acad Sci, Beijing Natl Lab Mol Sci, Inst Chem, CAS Key Lab Organ Solids, Beijing 100190, Peoples R China
[3] Xi An Jiao Tong Univ, State Key Lab Mech Behav Mat, Xian 710049, Peoples R China
基金
中国国家自然科学基金;
关键词
FIELD-EFFECT TRANSISTORS; POWER CONVERSION EFFICIENCY; ELECTRON-ACCEPTORS; ORGANIC PHOTOVOLTAICS; RANDOM COPOLYMERS; RING-FUSION; PERFORMANCE; MOBILITY; DONOR; SEMICONDUCTORS;
D O I
10.1039/c7py00444c
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
In this work, we present a new strategy to use fused and twisted conjugated backbones to construct conjugated small molecules and polymers as electron acceptors for non-fullerene solar cells. The new conjugated materials containing binary perylene bisimide (PBI) units linked with coplanar thieno[3,2-b]thiophene (as trans-PBI) or twisted thieno[2,3-b]thiophene (as cis-PBI) and the corresponding conjugated polymer cis-polyPBI were developed. A fused conjugated backbone ensures good charge transport, in which the twisted polymer cis-polyPBI was found to show the highest electron mobility of 1.2 x 10(-2) cm(2) V-1 s(-1) in field-effect transistors. Meanwhile, a twisted conjugated backbone effectively prevents the aggregation and crystallization of PBI units, resulting in isotropic charge transport and finely tuned micro-phase separation in bulk-heterojunction thin films. The high electron mobility and isotropic crystallinity make the fused and twisted electron acceptors achieve high power conversion efficiencies above 6% in non-fullerene solar cells, while the coplanar molecule trans-PBI as the electron acceptor shows a very low efficiency of 0.13%.
引用
收藏
页码:3300 / 3306
页数:7
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