Improving the nanoscale morphology and processibility for PCDTBT-based polymer solar cells via solvent mixtures

被引:40
作者
Fang, Gang [1 ]
Liu, Jian [1 ]
Fu, Yingying [1 ]
Meng, Bin [1 ]
Zhang, Baohua [1 ]
Xie, Zhiyuan [1 ]
Wang, Lixiang [1 ]
机构
[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Polymer Phys & Chem, Grad Sch, Changchun 130022, Peoples R China
基金
中国国家自然科学基金;
关键词
Polymer solar cells; Phase separation; Solvent mixtures; Thick active layer; PHOTOVOLTAIC CELLS; EFFICIENCY; ENHANCEMENT; NETWORK;
D O I
10.1016/j.orgel.2012.08.003
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The effect of solvent mixtures on the morphologies of poly[N-9'-hepta-decanyl-2,7-carbazole-alt-5,5-(4',7'-di-2-thienyl-2',1',3'-benzothiadiazole)] (PCDTBT):[6,6]-phenyl C-71-butyric acid methyl ester (PC71BM) blend films is investigated. 1,2,4-Trichlorobenzene (TCB) which is a good solvent for PCDTBT is selected to mix with chloroform (CF), chlorobenzene (CB) and o-dichlorobenzene (oDCB) for tuning the morphology of the PCDTBT:PC71BM blend. It is found that formation of nanoscale phase separation with a fibrillar PCDTBT nanostructure of PCDTBT:PC71BM blend which is favorable for exciton separation and charge carrier transport is strongly dependent on the solubility parameters of the solvent mixtures. A clearly defined nanoscale phase separation of the PCDTBT:PC71BM blend can be obtained with TCB:CF mixture. The resulted morphology is similar to that produced with sole DCB solvent that is currently the best solvent for PCDTBT:PC71BM blend solar cells. Moreover, the TCB:CF mixture demonstrates better solubility and processibility for PCDTBT:PC71BM blend and allows us to prepare thick active layer that is required in large-area roll-to-roll process. The polymer solar cells with 250 nm- thick active layer are fabricated by using TCB:CF solvent mixture and the power conversion efficiency of the devices reaches 6.45%. A highest short-circuit current of 13.6 mA/cm(2) is achieved due to enhanced optical absorption of thick active layer. (C) 2012 Elsevier B.V. All rights reserved.
引用
收藏
页码:2733 / 2740
页数:8
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