Electrochemical Study of Selenocystine Reactivity and Reduction at Metallic Surfaces

Abstract The reduction of seleno‐L‐cystine is examined on gold and platinum electrodes in aqueous solution. The voltammetric behavior is indicative of a two‐step process, in which the metallic substrate is modified by the diselenide analyte prior to observation of diffusionally controlled, proton‐coupled electron transfer. X‐ray photoelectron spectroscopy confirms the presence of selenium on gold foil samples that have been reductively cycled in selenocystine solution. The selenium‐based surface modification, which is accessible through multiple preparation routes, can be removed by anodic stripping and fully restored through subsequent cycling. The described electrochemical approach allows for the analysis of redox‐active chalcogen‐containing species under physiologically relevant conditions.