Polymer bulk heterojunction photovoltaic devices based on complex donors and solution-processable functionalized graphene oxide

被引:25
|
作者
Wang, Jigang [1 ]
Wang, Yongsheng [1 ]
He, Dawei [1 ]
Liu, Zhiyong [1 ]
Wu, Hongpeng [1 ]
Wang, Haiteng [1 ]
Zhou, Pan [1 ]
Fu, Ming [1 ]
机构
[1] Beijing Jiao Tong Univ, Inst Optoelect Technol, Minist Educ, Key Lab Luminescence & Opt Informat, Beijing 100044, Peoples R China
关键词
Bulk heterojunction; Organic polymer; Solar cells; Graphene; Complex donors; SOLAR-CELLS; NETWORK;
D O I
10.1016/j.solmat.2011.09.005
中图分类号
TE [石油、天然气工业]; TK [能源与动力工程];
学科分类号
0807 ; 0820 ;
摘要
Herein we report a study of the doping of the poly(2-methoxy-5-(30,70-dimethyloctyloxy)-1,4-phenylenevinylene) (MDMO-PPV), poly (3-oc tylthiophene) (P3OT), to the organic photovoltaic devices based on poly (3-hexylthiophene) (P3HT) and graphene derivative bulk heterojunction structure (BHJ). The addition of the donor polymers to P3HT:Graphene BJT solar cells resulted in a more broad absorption range. The interrelationships between UV-vis absorption, fill factor (FF), energy conversion efficiency (ECE) and current density have been simulated. Dependency of the open-circuit voltage (Voc) was based on different doped donors, which is due to the band structure of BHJ where the energy level difference between the highest occupied molecular orbital (HOMO) of the co-donors and the lowest occupied molecular orbital (LUMO) of the solution-processable functionalized graphene oxide (SPFGO) as acceptor was increased. The investigation indicated that the ECE of the co-donors:SPFGO BHJ solar devices with moderate doped donor amount can be influenced by the change of molecular packing structure, which can be interpreted in terms of incorporating doped donor. The XRD investigation of the complex donors/graphene BHJ solar device showed a well-organized intraplane structure with lamellae oriented normal to the substrate. In addition, The SEM investigation indicated the surface roughness morphology of the hybrid active layer film. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:58 / 65
页数:8
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