Electrocatalytic activity under oscillatory regime: The electro-oxidation of formic acid on ordered Pt3Sn intermetallic phase

Nenhuma Miniatura disponível

Data

2013-01-05

Título da Revista

ISSN da Revista

Título de Volume

Editor

Resumo

Despite the considerable progress in the understanding of the mechanistic aspects of the oscillatory electro-oxidation of C1 molecules, there are apparently no systematic studies concerning the impact of surface modifiers on the oscillation dynamics. Herein we communicate on the oscillatory electro-oxidation of formic acid on ordered Pt3Sn intermetallic phase, and compare the results with those obtained on a polycrystalline platinum electrode. Overall, the obtained results were very reproducible, robust and allowed a detailed analysis on the correlation between the catalytic activity and the oscillation dynamics. The presence of Sn in the intermetallic electrode promotes drastic effects on the oscillatory dynamics. The decrease in the mean electrode potential and in the oscillation frequency, as well as the pronounced increase in the number oscillations (and also in the oscillation time), was discussed in connection with the substantial catalytic enhancement of the Pt3Sn towards the electro-oxidation of formic acid. The self-organized potential oscillations were used to probe the electrocatalytic activity of the Pt3Sn electrode and compare it with that for polycrystalline Pt. The presence of Sn resulted in a significant decrease (2-11 times, depending on the applied current) of the rate of surface poisoning. © 2012 Elsevier B.V.

Descrição

Palavras-chave

Electrocatalysis, Formic acid, Intermetallic phase, Oscillations, Platinum-tin, Applied current, Electrocatalytic activity, Electrode potentials, Mechanistic aspects, Oscillation frequency, Oscillatory dynamics, Oscillatory regimes, Polycrystalline, Polycrystalline platinum, Potential oscillations, Surface modifiers, Surface poisoning, Systematic study, Catalyst activity, Catalytic oxidation, Dynamics, Oxidation, Platinum, Tin

Como citar

Catalysis Communications, v. 30, p. 23-26.

Coleções