On the design of Pt based catalysts. Combining porous architecture with surface modification by Sn for electrocatalytic activity enhancement

被引:23
作者
Florez-Montano, Jonathan [1 ]
Garcia, Gonzalo [1 ]
Rodriguez, Jose L. [1 ]
Pastor, Elena [1 ]
Cappellari, Paula [2 ]
Planes, Gabriel A. [2 ]
机构
[1] Univ La Laguna, Inst Univ Mat & Nanotecnol, San Cristobal la Laguna 38071, Tenerife, Spain
[2] Univ Nacl Rio Cuarto, Dept Quim, RA-5800 Rio Cuarto, Argentina
关键词
DMFC; DEMS; Mesoporous electrodes; CO oxidation; Methanol oxidation; Pt-based materials; OXYGEN-REDUCTION CATALYSTS; TEMPERATURE FUEL-CELLS; CARBON-MONOXIDE; PT-SN; METHANOL OXIDATION; FORMIC-ACID; PLATINUM; ELECTROOXIDATION; CO; RUTHENIUM;
D O I
10.1016/j.jpowsour.2015.02.018
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
Metallic mesoporous (MP) catalysts with large surface area can be obtained in-situ, in a single step, by electrochemical reduction. In this work, the electrochemical behavior of MPPt and Sn modified mesoporous Pt (MPPt/Sn) was studied and compared with commercial carbon supported PtSn alloy (3:1). The electrochemical activity toward carbon monoxide and methanol oxidation reactions were evaluated by cyclic voltammetry and chronomperometry, whereas X-ray photoelectron spectroscopy was used to determine the surface composition and oxidation state of the atoms in the top layers of the catalysts. The analysis of methanol conversion to CO2 was performed with aid of differential electrochemical mass spectrometry (DEMS). Results reveal a better performance of the MPPt/Sn, which shows higher current density and energy conversion efficiency of fuel to CO2 than conventional carbon supported PtSn alloy (3:1). (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:34 / 44
页数:11
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