Sn-modified carbon-supported Pt nanoparticles synthesized using spontaneous deposition as electrocatalysts for direct alcohol fuel cells

被引:7
|
作者
Velazquez-Palenzuela, Amado [1 ]
Centellas, Francesc [1 ]
Brillas, Enric [1 ]
Antonio Garrido, Jose [1 ]
Arias, Conchita [1 ]
Maria Rodriguez, Rosa [1 ]
Cabot, Pere-Lluis [1 ]
机构
[1] Univ Barcelona, Lab Electroquim Mat & Medi Ambient, Dept Quim Fis, Fac Quim, E-08028 Barcelona, Spain
关键词
Electrocatalysis; Ethanol oxidation reaction; Methanol oxidation reaction; Sn-modified Pt nanoparticles; Spontaneous deposition; Direct alcohol fuel cells; METHANOL OXIDATION; PLATINUM; ETHANOL; ELECTROOXIDATION; MONOXIDE; CATALYSTS; SURFACE; ACID; UPD; CO;
D O I
10.1016/j.ijhydene.2013.09.146
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
Sn-modified carbon-supported Pt nanoparticles (Sn(Pt)/C electrocatalysts) were prepared by spontaneous deposition. Sn species were deposited on Pt/C by immersion in 2.0 x 10(-4) M SnCl2 + 0.1 M HClO4 for different times, which allowed achieving an adequate control of the coverage (theta). Cyclic voltammetry (CV) in 0.5 M H2SO4 was carried out to determine theta and to evaluate the Sn(Pt)/C performance. The activity towards the oxidation reactions of methanol (MOR) and ethanol (EOR) was analyzed using CV in 0.5 M H2SO4 + 1.0 M alcohol. A promotional effect for the MOR and the EOR after the partial coverage by the Sn species was shown, as indicated by the significant reduction of the overpotential and the higher oxidation currents in both cases. This activation was explained by the formation of hydroxylated species on the tin deposits, thus facilitating the removal of the adsorbed intermediates. The best performance was achieved for theta approximate to 0.3 in the case of the MOR and for theta approximate to 0.5 in the case of the EOR. The reaction pathway for both alcohols was analyzed according to the obtained kinetic parameters, which significantly depended on the coverage. Copyright (C) 2013, Hydrogen Energy Publications, LLC. Published by Elsevier Ltd. All rights reserved.
引用
收藏
页码:16418 / 16426
页数:9
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