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The surface characterization of coated titanium electrodes has been studied in a 0.5 mol dm −3 solution using cyclic voltammetry. The results showed that the surface state of all the electrodes is controlled by the redox transition of Ir(III)/Ir(IV). The voltammetric charge, the double-layer capacitance, and the electrochemical activity present similar variation with the composition of the oxide mixture, showing maximum values at 50-70% Ir. The high electrochemical activity of the electrode with 50-70% Ir is attributed to not only its good electrocatalytic effect but also its large electrochemically active surface area, especially the contribution of the inner surface.
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Xu et al. (2003) studied this question.
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