High methanol tolerance of carbon-supported Pt-Cr alloy nanoparticle electrocatalysts for oxygen reduction

被引:60
作者
Yang, H [1 ]
Alonso-Vante, N
Lamy, C
Akins, DL
机构
[1] Nanjing Univ Technol, Coll Chem & Chem Engn, Nanjing 210009, Peoples R China
[2] CUNY City Coll, CASI, New York, NY 10031 USA
[3] CUNY City Coll, Dept Chem, New York, NY 10031 USA
[4] Univ Poitiers, Lab Electrocatalysis, UMR 6503, CNRS, F-86022 Poitiers, France
关键词
D O I
10.1149/1.1862258
中图分类号
O646 [电化学、电解、磁化学];
学科分类号
081704 ;
摘要
The electrocatalytic reduction of oxygen on carbon-supported Pt-Cr (1:1) alloy nanoparticle catalysts with two different metal loadings prepared via a carbonyl route was investigated based on the porous thin-film rotating disk-ring electrode technique and compared with that on E-TEK Pt/C catalyst in pure and methanol-containing electrolytes. The as-prepared Pt-Cr alloy nanoparticles, which have single-phase disordered structures, are well dispersed on the surface of carbon with a narrow size distribution even at 40 wt % metal loading. Such catalysts are stable in air up to 600 degrees C. As compared to the Pt/C catalyst, the alloy catalysts showed slightly enhanced activity for the oxygen reduction reaction in pure acid electrolyte and significantly enhanced activity in the presence of methanol, and the ring-current measurements on the homemade catalysts showed a reduction in peroxide yield in pure acid solution. The enhanced activity could be ascribed to the effect of alloying on the initiation and extent of surface oxide formation. Oxygen reduction kinetic analysis indicated a potential dependence of the apparent number of electrons transferred per oxygen molecule during the reduction in methanol-containing solution. High methanol tolerance of Pt-Cr alloy catalysts during the oxygen reduction could be explained well by the lower reactivity of methanol oxidation, which may originate from the composition effect and the dAll rights reserved.ordered structure of the alloy catalysts. (c) 2005 The Electrochemical Society.
引用
收藏
页码:A704 / A709
页数:6
相关论文
共 30 条
[1]   On the origin of the selectivity of oxygen reduction of ruthenium-containing electrocatalysts in methanol-containing electrolyte [J].
Alonso-Vante, N ;
Bogdanoff, P ;
Tributsch, H .
JOURNAL OF CATALYSIS, 2000, 190 (02) :240-246
[2]   Formation of carbon-supported PtM alloys for low temperature fuel cells: a review [J].
Antolini, E .
MATERIALS CHEMISTRY AND PHYSICS, 2003, 78 (03) :563-573
[3]   Electrocatalysis of oxygen reduction on a carbon supported platinum-vanadium alloy in polymer electrolyte fuel cells [J].
Antolini, E ;
Passos, RR ;
Ticianelli, EA .
ELECTROCHIMICA ACTA, 2002, 48 (03) :263-270
[4]  
Aricò AS, 1998, ELECTROCHEM SOLID ST, V1, P66, DOI 10.1149/1.1390638
[5]   THE STRUCTURE AND ACTIVITY OF PT-CO ALLOYS AS OXYGEN REDUCTION ELECTROCATALYSTS [J].
BEARD, BC ;
ROSS, PN .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1990, 137 (11) :3368-3374
[6]   Structural and electrochemical studies of Pt-Sn nanoparticulate catalysts [J].
Boucher, AC ;
Alonso-Vante, N ;
Dassenoy, F ;
Vogel, W .
LANGMUIR, 2003, 19 (26) :10885-10891
[7]   THE INFLUENCE OF METHANOL ON O(2) ELECTROREDUCTION AT A ROTATING PT DISK ELECTRODE IN ACID ELECTROLYTE [J].
CHU, D ;
GILMAN, S .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 1994, 141 (07) :1770-1773
[8]   Electrodes modified by electrodeposition of CoTAA complexes as selective oxygen cathodes in a direct methanol fuel cell [J].
Convert, P ;
Coutanceau, C ;
Crouïgneau, P ;
Gloaguen, F ;
Lamy, C .
JOURNAL OF APPLIED ELECTROCHEMISTRY, 2001, 31 (09) :945-952
[9]   Preparation of a Pt-Ru/C catalyst from carbonyl complexes for fuel cell applications [J].
Dickinson, AJ ;
Carrette, LPL ;
Collins, JA ;
Friedrich, KA ;
Stimming, U .
ELECTROCHIMICA ACTA, 2002, 47 (22-23) :3733-3739
[10]   Oxygen reduction at Pt and Pt70Ni30 in H2SO4/CH3OH solution [J].
Drillet, JF ;
Ee, A ;
Friedemann, J ;
Kötz, R ;
Schnyder, B ;
Schmidt, VM .
ELECTROCHIMICA ACTA, 2002, 47 (12) :1983-1988