Pt-, PtNi- and PtCo-supported catalysts for oxygen reduction in PEM fuel cells

被引:140
作者
Travitsky, N.
Ripenbein, T.
Golodnitsky, D.
Rosenberg, Y.
Burshtein, L.
Peled, E. [1 ]
机构
[1] Tel Aviv Univ, Sackler Fac Exact Sci, Sch Chem, IL-69978 Tel Aviv, Israel
[2] Tel Aviv Univ, Wolfson Appl Mat Res Ctr, IL-69978 Tel Aviv, Israel
关键词
supported; platinum; cobalt; nickel; catalyst; fuel cell;
D O I
10.1016/j.jpowsour.2006.05.035
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
The most widely used supporting material for ORR catalysts is high-surface-area carbon (such as Vulcan XC-72). However, at elevated temperatures, burning of the carbon-to-catalyst contact takes place and drying out of the cathode may destroy the three-phase zones. In order to avoid these problems, Pt catalysts supported on silica were synthesized and characterized parallel to those supported on carbon. In a search for more active and stable catalysts, in addition to supported Pt powders, we have synthesized and characterized carbon- and silica-supported PtNi and PtCo catalysts via the same electroless-deposition route. In order to avoid agglomeration of the platinum particles, a classic three-step electroless deposition (sensitization and activation, nucleation and growth) on silica and XC-72 was used for the first time. The PtNi- and the PtCo-supported catalysts have smaller crystal size (as low as 2.2 nm) and larger electrochemical surface area (up to 57 m(2) g(-1)) than do pure Pt-supported catalysts. The stability of the alloy catalysts in acidic medium was tested. Catalysts post-treated in acid were found to be stable and had a platinum-rich (or pure) "skin" structure. Some conclusions were drawn regarding catalyst structure and corrosion mechanism. (c) 2006 Elsevier B.V. All rights reserved.
引用
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页码:782 / 789
页数:8
相关论文
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