Kinetic analysis of the hydrogen oxidation reaction at Nafion film covered Pt-black rotating disk electrodes

Ren-Bin Lin , Shin-Min Shih
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引用次数: 10

Abstract

The kinetics of the H2 oxidation reaction at Nafion film covered Pt-black rotating disk electrodes (RDEs) in 0.5 M H2SO4 at 298 K was investigated by varying the Pt loading, Nafion film thickness, and rotating rate. The equation describing the H2 oxidation kinetics at an RDE with a Nafion film covered porous Pt layer was derived, assuming a Tafel–Volmer mechanism and taking into account the mass transfer resistances in the aqueous electrolyte, Nafion film, and Pt layer. The H2 oxidation reaction at the Pt layer was proved to be reversible and the measurable current density was determined entirely by the mass transfer of H2 in the aqueous electrolyte and the Nafion film; the apparent kinetic current density measured was due to the experimental error. More accurate results of kinetic analysis were obtained in this work than our results reported previously.

Pt-black旋转圆盘电极上的氢氧化反应动力学分析
通过改变Pt负载、Nafion膜厚度和旋转速率,研究了Pt-black旋转圆盘电极(RDEs)在0.5 M H2SO4和298 K条件下的H2氧化反应动力学。在假设Tafel-Volmer机制并考虑水溶液电解质、Nafion膜和Pt层的传质阻力的情况下,推导了多孔Pt层覆盖Nafion膜的RDE中H2氧化动力学方程。Pt层的H2氧化反应是可逆的,可测电流密度完全由H2在水溶液电解质和Nafion膜中的传质决定;测量的表观动态电流密度是由于实验误差造成的。本文得到的动力学分析结果比以往报道的结果更准确。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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