A comparative study of Pt/C and Pt-MoOx/C catalysts with various compositions for methanol electro-oxidation

被引：65

作者：

Ma, Liang ^{[1
,2
]}

Zhao, Xiao ^{[1
,2
]}

Si, Fengzhan ^{[1
,2
]}

Liu, Changpeng ^{[1
]}

Liao, Jianhui ^{[1
]}

Liang, Liang ^{[1
]}

Xing, Wei ^{[1
]}

机构：

[1] Chinese Acad Sci, Changchun Inst Appl Chem, State Key Lab Electroanalyt Chem, Changchun 130022, Peoples R China

[2] Chinese Acad Sci, Grad Univ, Beijing 100049, Peoples R China

来源：

ELECTROCHIMICA ACTA | 2010年 / 55卷 / 28期

基金：

中国国家自然科学基金;

关键词：

Pt-MoOx/C; Methanol electro oxidation; Mass activity; Specific activity; Electrocatalyst; Metal-support interaction; CARBON-SUPPORTED PLATINUM; ENHANCED CO-TOLERANCE; MEMBRANE FUEL-CELLS; ANODE CATALYST; FORMIC-ACID; RU ELECTROCATALYST; H-2/CO MIXTURES; OXIDATION; ALLOY; NANOPARTICLES;

D O I：

10.1016/j.electacta.2010.08.034

中图分类号：

O646 [电化学、电解、磁化学];

学科分类号：

081704 ;

摘要：

The methanol electro-oxidation behaviors on the Pt-MoOx/C catalysts with various compositions were investigated and compared to those of Pt/C catalyst by cyclic voltammetry and chronoamperometry The Pt-MoOx/C catalysts were prepared by depositing Pt on the MoOx/C support obtained by precipitation-reduction method in advance The physical properties of the prepared catalysts were characterized by XRD XPS EDX and TEM From the results of XRD and TEM it was shown that the MoOx/C support facilitated the dispersion of Pt particles All the Pt-MoOx/C catalysts showed relative lower Mo contents comparing to their nominal values No PtMo alloy was formed in these catalysts which were affirmed by XPS and XRD It was found that all the Pt-MoOx/C catalysts showed higher mass activity (normalized to the mass of Pt) but lower specific activity (normalized to the electrochemical active surface areas) for methanol oxidation than the Pt/C catalyst With the increase of Mo contents in Pt-MoOx/C catalysts the activities of Pt-MoOx/C catalysts decreased Combined with the composition and structure analyses the differences in methanol oxidation on these catalysts were attributed to the interaction between the Pt particles and the MoOx/C support It was suggested that the Pt metal-MoOx/C support interaction resulted in two effects One was decreasing the Pt particle size the other was decreasing the specific activities of these catalysts for methanol oxidation Comprising these two contradictory effects the mass activities of these catalysts for methanol oxidation increased (C) 2010 Elsevier Ltd All rights reserved

引用

页码：9105 / 9112

页数：8

共 44 条

[1]

Aricò AS, 2001, FUEL CELLS, V1, P133

[2] Surface structure effects in platinum/ruthenium methanol oxidation electrocatalysis [J].