Tailoring a Pt-Ru catalyst for enhanced methanol electro-oxidation

被引:78
|
作者
Raman, R. K.
Shukla, A. K. [1 ]
Gayen, A.
Hegde, M. S.
Priolkar, K. R.
Sarode, P. R.
Emura, S.
机构
[1] Indian Inst Sci, Solid State & Struct Chem Unit, Bangalore 560012, Karnataka, India
[2] Goa Univ, Dept Phys, Taleigao Plateau 403206, Goa, India
[3] Osaka Univ, Inst Sci & Ind Res, Ibaraki, Osaka 5670047, Japan
[4] Cent Electrochem Res Inst, Karaikkudi 630006, Tamil Nadu, India
关键词
methanol electro-oxidation; direct methanol fuel cell; electron microscopy; photoelectron spectroscopy; X-ray absorption spectroscopy;
D O I
10.1016/j.jpowsour.2005.06.031
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
A carbon-supported (1:1) Pt-Ru (Pt-Ru/C) alloy catalyst has been prepared in-house by the sulfito-complex route, and has been tailored to achieve enhanced activity towards methanol electro-oxidation by annealing it at varying temperatures in air. The catalyst samples annealed between 250 and 300 degrees C in air for 30 min exhibit superior catalytic activity towards methanol electro-oxidation in a solid-polymer-electrolyte direct methanol fuel cell (SPE-DMFCs) operating at 90 degrees C. Both the as-prepared and annealed Pt-Ru/C catalysts have been characterized by powder X-ray diffraction (XRD), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), extended X-ray absorption fine structure (EXAFS), and cyclic voltammetry. It is conjectured that while annealing the Pt-Ru/C catalysts, both Pt-Pt and Pt-Ru bonds increase whereas the Pt-O bond shrinks. This is accompanied with a positive variation in Ru/Pt metal ratio suggesting the diffusion of Ru metal from the bulk catalyst to surface with an increase in oxidic ruthenium content. Such a treatment appears seminal for enhancing the electrochemical activity of Pt-Ru catalysts towards methanol oxidation. (c) 2005 Elsevier B.V. All rights reserved.
引用
收藏
页码:45 / 55
页数:11
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