电极
铂金
化学
电化学
氧化物
无机化学
电极电位
反应速率常数
标准氢电极
亚硝酸盐
标准电极电位
工作电极
钯氢电极
下降(电信)
参比电极
分析化学(期刊)
动力学
催化作用
物理化学
有机化学
硝酸盐
电信
物理
量子力学
计算机科学
作者
Barbara Piela,Piotr Piela,Piotr K. Wrona
出处
期刊:Journal of The Electrochemical Society
[The Electrochemical Society]
日期:2002-01-01
卷期号:149 (10): E357-E357
被引量:22
摘要
The nitrite oxidation process was reinvestigated at rotating gold and platinum electrodes covered by an oxide layer. The electrochemical properties of the surface oxides were determined by recording the coverage curves of the gold and platinum electrodes at various pH values and for different experiment durations. The reaction mechanism on the oxidized surface was found to be the same as that on the oxide-free surface. The sole effect of the surface oxide was a drop of the standard rate constant of the electrode reaction which was a function of the surface coverage by the oxide. Nitrite oxidation on the oxide-covered electrodes was found to proceed via the innersphere mechanism with inhibitor adsorption on an energetically uniform surface. The kinetic results obtained for the gold and the platinum electrode were almost the same. The complicated shape of rotating disk voltammograms was explained in terms of the increase of the rate of the electrode reaction with increasing electrode potential and the drop of the standard rate constant of the electrode reaction with increasing electrode potential due to the increase of the oxide coverage with electrode potential, the latter process being dependent on the electrode material, pH, and time (scan rate). © 2002 The Electrochemical Society. All rights reserved.
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