A simple electrochemical method has been established to detect a Cu
2O phase present or newly formed on the surface of a copper anode.Utilizing this technique, a study has been extended to investigate conditions which allow this oxide phase to form during anodization.
A well-defined peak corresponding to the reduction of a Cu
2O phase appears on the cathodic voltammetric curve provided a sufficiently fast potential-sweep rate is employed (i.e., <0.6 V/min). This reduction reaction proceeds through the following three sequential steps;{Cu
2O+2e-→2Cu°+O
2- (electron transfer)
Cu
2+O
2-→CuO (rate-determining)
CuO+H
2SO
4→CuSO
4+H
2O (following reaction)
The overall cathodic reacton is expressed by,
Cu
2O+Cu
2++2
e-→2Cu°+CuO
and its equilibrium potential as calculated from the Nernst's equation based on the present experimental conditions is-0.42V vs. Hg/Hg
2 SO
4, which coincides very well with the experimental value.
Various anodizing conditions were given to a pure Cu anode, and analysis of the results indicates that a Cu
20 phase only forms when the copper anode is passive.
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