Some unusual features of the electrochemistry of silver in aqueous base

Abstract

Multilayer oxide films were grown on silver in base by repetitive potential cycling; however, the type of oxide obtained, as assessed on the basis of its reduction behaviour, was dependent on the lower limit of the oxide growth cycles. Using limits of 1.03–2.60 V (RHE) the oxide film produced was assumed to be predominantly Ag₂O; reduction of the latter yielded a cathodic peak at ca. 0.8 V and a surface layer of silver microparticles of diameter ranging from ca. 100 to 227 nm which, although relatively stable, were prone to rapid, extensive reoxidation. Altering the oxide growth limits to 0.7–2.60 V resulted in the growth of a different type of oxide deposit which is assumed to be AgOH; reduction of the latter occurred in a negative sweep in a random manner, i.e. in the form of cathodic spikes extending to potentials as low as ca. –0.5 V. Both types of silver oxide species are assumed to be involved in premonolayer oxidation and electrocatalysis at silver in base and the nature of the former process is discussed in some detail.