Pt-Sn/C catalysts prepared by sodium borohydride reduction for alcohol oxidation in fuel cells: Effect of the precursor addition order

被引:41
作者
Lopez-Suarez, F. E. [1 ]
Bueno-Lopez, A. [2 ]
Eguiluz, K. I. B. [1 ]
Salazar-Banda, G. R. [1 ]
机构
[1] Univ Tiradentes, Res & Technol Inst Proc Engn Postgrad PEP, Electrochem & Nanotechnol Lab, Aracaju, SE, Brazil
[2] Univ Alicante, Fac Sci, Dept Inorgan Chem, MCMA Grp, E-03080 Alicante, Spain
关键词
Platinum; Tin; Ethanol oxidation reaction; Electrocatalysis; Fuel cell; ETHANOL OXIDATION; ANODE CATALYSTS; METHANOL ELECTROOXIDATION; CARBON-MONOXIDE; FORMIC-ACID; ELECTROCATALYSTS; METAL; NANOPARTICLES; BEHAVIOR; ALLOY;
D O I
10.1016/j.jpowsour.2014.06.042
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 series of Pt-Sn/C catalysts used as anodes during ethanol oxidation are synthesized by a deposition process using NaBH4 as the reducing agent. The order in which the precursors are added affects the electrocatalytic activity and physical-chemical characteristics of the bimetallic catalysts, where the Pt-Sn catalyst prepared by co-precipitation of both metals functions best below a potential of 0.5 V and the catalyst prepared by sequential deposition of Sn and Pt (drying after Sn addition) is most active above a potential of 0.5 V. The electrochemical behavior of catalysts during ethanol oxidation in an acidic medium are characterized and monitored in a half-cell test at room temperature by cyclic voltammetry, chronoamperometry and anode potentiostatic polarization. Catalyst structure and chemical composition are investigated by transmission electron microscopy (TEM), X-ray powder diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). This behavior presented for best Pt-Sn catalyst can be attributed to the so-called bifunctional mechanism and to the electronic interaction between Pt and Sn. (C) 2014 Elsevier B.V. All rights reserved.
引用
收藏
页码:225 / 232
页数:8
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