Abstract

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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