Synthesis and simultaneously enhanced photovoltaic property of poly [4,4,9,9-tetra(4-octyloxyphenyl)-2,7-indaceno[1,2-b:5,6-b′]dithiophene-alt-2,5-thieno[3,2-b]thiophene]

被引:20
作者
Xia, Yangjun [1 ]
Gao, Yuanyuan [2 ]
Zhang, Yong [3 ]
Tong, Junfeng [1 ]
Li, Jianfeng [1 ]
Li, Huijuan [2 ]
Chen, Dejia [2 ]
Fan, Duowang [1 ]
机构
[1] Lanzhou Jiaotong Univ, Key Lab Optoelect Technol & Intelligent Control, Minist Educ, Lanzhou 730070, Peoples R China
[2] Lanzhou Jiaotong Univ, Coll Chem & Biol Engn, Lanzhou 730070, Peoples R China
[3] S China Normal Univ, Inst Optoelect Mat & Technol, Guangzhou 510631, Guangdong, Peoples R China
基金
中国博士后科学基金; 中国国家自然科学基金;
关键词
Indaceno[1,2-b:5,6-b ']dithiophene; Photovoltaic cells; Thieno[3,2-b]thiophene; OPEN-CIRCUIT VOLTAGE; SOLAR-CELLS; SEMICONDUCTING POLYMERS; CONJUGATED POLYMERS; TANDEM POLYMER; BANDGAP; COPOLYMERS; BENZODITHIOPHENE; DERIVATIVES; BITHIOPHENE;
D O I
10.1016/j.polymer.2012.12.006
中图分类号
O63 [高分子化学(高聚物)];
学科分类号
070305 ; 080501 ; 081704 ;
摘要
An alternating conjugated polymer derived from 4,4,9,9-tetra(4-octyloxyphenyl)indaceno[1,2-b:5,6-b'] dithiophene and thieno[3,2-b]thiophene was synthesized by Stille coupling reaction. The copolymer shows extensive absorption from 360 nm to 590 nm with optical band gap of 2.12 eV. The highest occupied molecular orbit (HOMO) and the lowest unoccupied molecular orbit (LUMO) energy levels of the copolymer, determined by cyclic voltammetry (CV), are about -5.29 eV and -3.01 eV, respectively. A field-effect hole mobility of 8.1 x 10(-4) cm(2)/(V s) and an on/off ratio of 2.0 x 10(3) are obtained in the field-effect transistors based on the copolymer. The J(sc), V-oc and FF of the polymer photovoltaic cells (PVCs) based on the copolymer were enhanced simultaneously via the inserting of alcohol soluble conjugated polymer interlayer between active layer and metal cathode, and the maximal power conversion efficiency of 4.19% was achieved in the modified devices under an AM 1.5 simulator (100 mWcm(-2)). (C) 2012 Elsevier Ltd. All rights reserved.
引用
收藏
页码:607 / 613
页数:7
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