Recent advances in alloy counter electrodes for dye-sensitized solar cells. A critical review

被引:106
作者
Tang, Qunwei [1 ,2 ]
Duan, Jialong [2 ]
Duan, Yanyan [1 ,3 ]
He, Benlin [2 ]
Yu, Liangmin [1 ,3 ]
机构
[1] Ocean Univ China, Minist Educ, Key Lab Marine Chem Theory & Technol, Qingdao 266100, Peoples R China
[2] Ocean Univ China, Inst Mat Sci & Engn, Qingdao 266100, Peoples R China
[3] Ocean Univ China, Qingdao Collaborat Innovat Ctr Marine Sci & Techn, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Dye-sensitized solar cell; Counter electrode; Alloy electrocatalyst; Electrocatalytic reaction; COMPLEX/GRAPHENE OXIDE MULTILAYERS; NITROGEN-DOPED GRAPHENE; IN-SITU GROWTH; CARBON NANOTUBES; HIGH-EFFICIENCY; LOW-COST; CHARGE-TRANSFER; POLYPYRROLE NANOPARTICLES; FUNCTIONALIZED GRAPHENE; TITANIUM-DIOXIDE;
D O I
10.1016/j.electacta.2015.08.072
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
Dye-sensitized solar cell (DSSC) has been considered as a potentially cost-effective alternative to silicon solar cell. By optimizing three components of a typical DSSC including a dye-sensitized wide-bandgap semiconductor photoanode for creating and transporting electrons, n redox electrolyte, and a counter electrode (CE) for reducing oxidized species in electrolyte, a maximum power conversion efficiency of 13% has been determined. The high cost of DSSCs is to a large part dictated by the high loading of Pt required to catalyze the triiodide reduction reaction. Arguably one of the arising routes to reduce fabrication cost of DSSCs with no sacrifice of catalytic activity of CEs is to alloy Pt with other metals/ nonmetals or to replace Pt with Pt-free alloys. In this perspective paper, we outline the advances of alloy CEs in comparison with other alternatives such as carbonaceous materials and conductive polymers and their hybrids including design concepts, fabrication approaches, and properties. Finally, this review launches prospects and challenges of promising alloy CEs for their applications in high-efficiency DSSCs. (C) 2015 Elsevier Ltd. All rights reserved.
引用
收藏
页码:886 / 899
页数:14
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