Abstract

AbstractReversible, oxidative adsorption of hydrosulfide (HS−) and ethanethiolate (CH3CH2S−) on highly‐ordered, Ag(111) electrodes in aqueous 0.5 M NaOH solutions is reported. Oxidation of HS− and CH3CH2S− results in adlayer formation, as determined by voltammetry, coulometry, and in‐situ electrochemical quartz‐crystal measurements. The voltammetric response of Ag(111) in HS− solutions displays three characteristic waves. Two waves correspond to the reversible 1‐e− oxidative adsorption of HS”, resulting in the formation of a Ag‐SH adlayer. The third wave corresponds to the kinetically‐slow 1‐e− oxidation of the Ag‐SH adlayer, yielding an underpotential deposited monolayer of Ag2S. The voltammetric response observed in CH3CH2S− solutions is qualitatively similar to that of HS−, displaying two well‐resolved waves corresponding to oxidative adsorption. The observation of two voltammetric waves is suggestive of a mechanism of CH3CH2S− adlayer formation involving at least two distinct structural phases. However, unlike the situation for HS”, the resulting Ag‐SCH2CH3 adlayer is unable to undergo a second oxidative transition. The free energies of adsorption of HS” and CH3CH2S− on Ag(111) are measured to be ca. −23 kcal/mol.

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