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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%.
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页码:3300 / 3306
页数:7
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