Abstract

The electrochemical behaviour of a copper coated p-type InP electrode has been investigated. The copper coating was obtained by electrodeposition from a Cu 2+ containing sulfuric acid solution under illumination. This reduction reaction can compete with H + reduction and with its side reaction, the cathodic decomposition of InP, depending on the illumination level, on the Cu 2+ concentration in the electrolyte, and on the rotation speed of the electrode. It appears that when the amount of Cu 2+ at the InP|electrolyte interface is sufficient to convert the whole flux of the photocarriers, the Cu 2+ reduction becomes the main photoprocess, hindering the hydrogen evolution and the cathodic decomposition. A metal deposit up to about 100 equivalent monolayers can form on the electrode surface without any decrease of the photocurrent, as a result of a non-uniform coverage rate of the metal.

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