Abstract

In this paper the thermodynamic data for complex formation between Ag+ and S2O32− ions, determined previously, are applied to kinetic investigation of the reduction of silver thiosulphate complexes. Both electrochemical (linear sweep voltammetry on a rotating disc electrode) and surface analytical (Auger electron spectroscopy) techniques are used. The deposits resulting from the electrodeposition of silver thiosulphate complexes are shown to be composed of silver and to be polycrystalline. The reduction follows a mechanism involving mass and charge transfer and chemical reaction steps. The relevant kinetic parameters are calculated and a rate equation describing the kinetics of the reduction is given.

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