Economical Pt-Free Catalysts for Counter Electrodes of Dye-Sensitized Solar Cells

Mingxing Wu(Dalian University of Technology), Xiao Lin(Dalian University of Technology), Yudi Wang(Dalian University), Liang Wang(Dalian University of Technology), Wei Guo(Dalian University), Daidi Qi(Dalian University of Technology), Xiaojun Peng(Dalian University), Anders Hagfeldt(Uppsala University), Michaël Grätzel(École Polytechnique Fédérale de Lausanne), Tingli Ma(Dalian University)
Journal of the American Chemical Society
January 23, 2012
Cited by 839Open Access
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Abstract

Three classes (carbides, nitrides and oxides) of nanoscaled early-transition-metal catalysts have been proposed to replace the expensive Pt catalyst as counter electrodes (CEs) in dye-sensitized solar cells (DSCs). Of these catalysts, Cr(3)C(2), CrN, VC(N), VN, TiC, TiC(N), TiN, and V(2)O(3) all showed excellent catalytic activity for the reduction of I(3)(-) to I(-) in the electrolyte. Further, VC embedded in mesoporous carbon (VC-MC) was prepared through in situ synthesis. The I(3)(-)/I(-) DSC based on the VC-MC CE reached a high power conversion efficiency (PCE) of 7.63%, comparable to the photovoltaic performance of the DSC using a Pt CE (7.50%). In addition, the carbide catalysts demonstrated catalytic activity higher than that of Pt for the regeneration of a new organic redox couple of T(2)/T(-). The T(2)/T(-) DSCs using TiC and VC-MC CEs showed PCEs of 4.96 and 5.15%, much higher than that of the DSC using a Pt CE (3.66%). This work expands the list of potential CE catalysts, which can help reduce the cost of DSCs and thereby encourage their fundamental research and commercial application.


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