In Situ Synthesized Economical Tungsten Dioxide Imbedded in Mesoporous Carbon for Dye-Sensitized Solar Cells As Counter Electrode Catalyst

被引:56
|
作者
Wu, Mingxing [1 ]
Lin, Xiao [1 ]
Wang, Liang [1 ]
Guo, Wei [1 ]
Wang, Yudi [1 ]
Xiao, Jinqiu [1 ]
Hagfeldt, Anders [2 ]
Ma, Tingli [1 ]
机构
[1] Dalian Univ Technol, Sch Chem Engn, State Key Lab Fine Chem, Dalian 116024, Liaoning Provin, Peoples R China
[2] Uppsala Univ, Dept Phys & Analyt Chem, SE-75105 Uppsala, Sweden
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2011年 / 115卷 / 45期
基金
中国国家自然科学基金;
关键词
D O I
10.1021/jp205886d
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Tungsten dioxide imbedded in mesoporous carbon (WO2-MC) was obtained by in situ synthesis and then introduced into dye-sensitized solar cells (DSCs) as a counter electrode (CE) catalyst. Catalytic activity for redox couple regeneration was improved significantly through combining high electrical conductivity and catalytic activity into one material, WO2-MC, in which WO2 served as a catalyst and MC served as an electrical conductor. This has been proved by cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). The triiodide/iodide-based DSC using WO2-MC as CE showed a high power conversion efficiency (PCE) of 7.76%, which surpassed the performance of the DSC using traditional Pt CE (7.55%). In addition, the WO2-MC and WO2 nanorods exhibited higher catalytic activity than Pt for the regeneration of a new organic redox couple, di-5-(1-methyltetrazole) disulfide/5-mercapto-1-methyltetrazole N-tetramethylammonium salt (T-2/T-). The PCE of the T-2/T--based DSCs using WO2-MC, WO2, and Pt were 5.22, 4.66, and 3.09%, respectively.
引用
收藏
页码:22598 / 22602
页数:5
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