Abstract
Two aspects of the electrochemical behavior of Hg1−xCdxTe in anodizing solution are presented. The current-voltage relationship for anodically oxidized Hg1−xCdxTe under cathodic bias has been examined and found to be independent of film thickness or substrate composition and carrier type for oxides exceeding 100 Å thick. For samples in solution biased anodically, ultraviolet light absorption results in increased electrode current. Mechanisms for these effects are discussed.
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