Abstract
The electrodissolution of Au(111) in anaerobic cupric/ammonia/thiosulfate solutions, typical of a non-equilibrium dissipative system, was investigated via in situ electrochemical atomic force microscopy. At a specific initial concentration ratio of aqueous ammonia to cupric ions, the pit number and average pit area increase autocatalytically, while the pit depth increases monotonically during dissolution. A further increase in this initial concentration ratio leads to oscillatory dynamics in the pit number and average pit area while the pit depth fluctuates between one and two atoms. Mechanistic analysis indicates that alternation between formation and dissolution of a sulfur film results in periodic pitting, which produces gold dissolution layer by layer. This work presents a new dissolution mode, i.e., periodic layer dissolution generated by oscillatory pitting processes in addition to a pitting mode with a continually increasing depth, and the use of high initial concentration ratios of ammonia to cupric ion to accelerate the elimination of passivating sulfur film for Au dissolution.
