Methanol oxidation on carbon-supported Pt-Ru-Ni ternary nanoparticle electrocatalysts

被引:66
作者
Liu, Juanying [1 ,2 ]
Cao, Jianyu [1 ,2 ]
Huang, Qinghong [1 ]
Li, Xiaowei [1 ]
Zou, Zhiqing [1 ]
Yang, Hui [1 ]
机构
[1] Chinese Acad Sci, Shanghai Inst Microsyst & Informat Technol, Energy Sci & Technol Lab, Shanghai 200050, Peoples R China
[2] Grad Univ, Chinese Acad Sci, Beijing 100039, Peoples R China
基金
中国国家自然科学基金;
关键词
methanol oxidation; electrocatalysis; alloy nanoparticle; hydroxyl Ru oxide; stability;
D O I
10.1016/j.jpowsour.2007.08.100
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
Methanol oxidation on carbon-supported Pt-Ru-Ni ternary alloy nanoparticles was investigated based on the porous thin-film electrode technique and compared with that on Johnson-Matthey Pt-Ru alloy catalyst. Emphasis is placed on the effect of alloying degree on the electrocatalytic activity and stability of the ternary catalysts. The as-prepared Pt-Ru-Ni nanoparticles exhibited a single phase fcc disordered structure, and a typical TEM image indicates that the mean diameter is ca. 2.2 nm, with a narrow particle size distribution. Also, the as prepared Pt-Ru-Ni catalysts exhibited significantly enhanced electrocatalytic activity and good stability for methanol oxidation in comparison to commercial Pt-Ru catalyst available from Johnson-Matthey. The highest activity of methanol oxidation on Pt-Ru-Ni catalysts was found with a Pt-Ru-Ni atomic ratio of 60:30: 10 and at a heat-treatment temperature of ca. 175 degrees C. The significantly enhanced catalytic activity for methanol oxidation is attributed to the high dispersion of the ternary catalyst, to the role of Ni as a promotion agent, and especially to the presence of hydroxyl Ru oxide. Moreover, the stability of the ternary nanocatalytic system was found to be greatly improved at heat-treatment temperatures higher than ca. 250 degrees C, likely due to a higher alloying degree at such temperatures for the ternary catalysts. (c) 2007 Elsevier B.V. All rights reserved.
引用
收藏
页码:159 / 165
页数:7
相关论文
共 43 条
[1]   Carbonyl tailored electrocatalysts [J].
Alonso-Vante, N. .
FUEL CELLS, 2006, 6 (3-4) :182-189
[2]  
Aricò AS, 2001, FUEL CELLS, V1, P133
[3]   INVESTIGATION OF A CARBON-SUPPORTED QUATERNARY PT-RU-SN-W CATALYST FOR DIRECT METHANOL FUEL-CELLS [J].
ARICO, AS ;
POLTARZEWSKI, Z ;
KIM, H ;
MORANA, A ;
GIORDANO, N ;
ANTONUCCI, V .
JOURNAL OF POWER SOURCES, 1995, 55 (02) :159-166
[4]   Active form of Ru for the CH3OH electro-oxidation reaction [J].
Bock, C ;
Collier, A ;
MacDougall, B .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2005, 152 (12) :A2291-A2299
[5]   The production of a high loading of almost monodispersed Pt nanoparticles on single-walled carbon nanotubes for methanol oxidation [J].
Cao, Jianyu ;
Du, Chong ;
Wang, Shiunchin C. ;
Mercier, Philippe ;
Zhang, Xigui ;
Yang, Hui ;
Akins, Daniel L. .
ELECTROCHEMISTRY COMMUNICATIONS, 2007, 9 (04) :735-740
[6]   Methanol oxidation on Pt/Ru, Pt/Ni, and Pt/Ru/Ni anode electrocatalysts at different temperatures for DMFCs [J].
Choi, JH ;
Park, KW ;
Kwon, BK ;
Sung, YE .
JOURNAL OF THE ELECTROCHEMICAL SOCIETY, 2003, 150 (07) :A973-A978
[7]   Surface structure effects in platinum/ruthenium methanol oxidation electrocatalysis [J].
Chrzanowski, W ;
Wieckowski, A .
LANGMUIR, 1998, 14 (08) :1967-1970
[8]   Pt-Sn/C electrocatalysts for methanol oxidation synthesized by reduction with formic acid [J].
Colmati, F ;
Antolini, E ;
Gonzalez, ER .
ELECTROCHIMICA ACTA, 2005, 50 (28) :5496-5503
[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]   Electrocatalysis in direct methanol fuel cells: in-situ probing of PtRu anode catalyst surfaces [J].
Dinh, HN ;
Ren, XM ;
Garzon, FH ;
Zelenay, P ;
Gottesfeld, S .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 2000, 491 (1-2) :222-233