Voltammetric measurements show reduced electrochemical activity in TiOx–Pt electrodes, suggesting implications for their use in energy conversion applications.
The electrochemical properties of TiOx–Pt electrodes with platinum loadings ranging from 0.3 to 2.0 mg/cm2, both as-deposited (non-heat-treated) and after annealing at 5000C for 3 h, were investigated. Voltammetric measurements were performed in 1 M HClO4. The cyclic voltammograms reveal that the cathodic reduction currents of oxygen-containing platinum species on annealed electrodes are 1.5–2 times lower than those on as-deposited ones, indicating a reduction in the true (active) surface area during heat treatment. The electrocatalytic activity of the prepared materials was evaluated toward the oxygen evolution reaction in 1 M HClO4. Pt-containing electrodes exhibit significantly lower oxygen evolution overpotentials compared to the TiOx electrodes. For as-deposited samples, the oxygen evolution overpotential decreases with increasing a platinum content in the coating. For annealed electrodes, a similar trend is observed. The overpotential for coatings with platinum content of 0.5 mg/cm2 and above remains unchanged. At a Pt loading of 0.3 mg/cm2, the metal layer is not continuous, and the material exhibits a porous structure with platinum islands on TiOx. In contrast, materials with Pt content of 0.5 mg/cm2 and higher maintain porosity, but the metal layer is continuous and uniform.
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Knysh et al. (2025) studied this question.
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