An XPS study on oxidation states of Pt and its alloys with Co and Cr and its relevance to electroreduction of oxygen

被引:348
作者
Aricò, AS
Shukla, AK
Kim, H
Park, S
Min, M
Antonucci, V
机构
[1] Inst CNR TAE, I-98126 Messina, Italy
[2] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[3] Seoul Natl Univ, Dept Chem, Ctr Mol Catalysis, Seoul 151742, South Korea
关键词
X-ray photoelectron spectroscopy; polymer-electrolyte fuel cell; solid-polymer-electrolyte direct methanol fuel cell; oxygen reduction; electrocatalysts; platinum-metal alloys;
D O I
10.1016/S0169-4332(00)00831-X
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
Cathodic reduction of oxygen in fuel cells is known to be enhanced on platinum alloys in relation to the platinum metal. The higher performance of the platinum alloys is as a result of the improved oxygen-reduction kinetics on the alloys but there is hardly any increase in the electrode platinum-surface-areas for the platinum alloys as compared to the platinum metal, and thus the higher performance is solely due to the enhanced electrocatalytic activity of the alloys as compared to the platinum metal. The present X-ray photoelectron spectroscopic (XPS) study on carbon-supported Pt, Pt-Co and Pt-Co-Cr electrocatalysts suggests the presence of a relatively lower Pt-oxide content on the: alloys. The: X-ray powder diffraction patterns for these electrocatalysts show that while the carbon-supported platinum electrocatalyst has a face-centered cubic (fcc) phase, carbon-supported Pt-Co and Pt-Co-Cr electrocatalysts: exhibit a face-centered tetragonal (fct) phase. But, Pt electrocatalyst has a lower particle-size and, hence, a higher dispersion. Previous studies have shown higher activities on the Pt-alloys than on Pt, and have attributed it to changes in the electronic and structural characteristics of Pt. These changes can be correlated with the lower oxidation-state of Pt sites, as found in this study. (C) 2001 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:33 / 40
页数:8
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