Deposition of platinum group metals is considered in relation to electrocatalysis of anodic fuel cell processes and reductive electrocatalysis of organic and inorganic reagents. For metallic materials, the roles of dispersion (specific surface area) and defectiveness can be easily separated by means of coulometric techniques. This experience can be applied to deposition of copper and copper-based alloys for carbon dioxide electrochemical reduction.
Deposition of oxides is addressed in the context of non-noble electrocatalysts for oxygen and hydrogen peroxide reactions, and also in relation to electrocatalytic processes for sensor applications. In addition to microstructural factors, oxygen stoichiometry is demonstrated to be important factor for electrocatalysis. Stoichiometry control by deposition potential is addressed in respect to oxide/solution equilibria as exampled by the data on tungsten and manganese oxides.
Finally, general principles and experimental approaches to quantify electrocatalytic activity of electrodeposited materials are considered. Namely, the techniques to determine current density normalized to the real surface area are discussed. The advantages of electrodeposited binder-free catalysts are listed and explained.
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