▎ 摘　　要

We report here redox reactions between graphene oxide (GO) and mercaptans, which reduces GO to reduced graphene oxide (RGO) and oxidizes mercaptans into disulfides. The reduction processes of GO using various mercaptans as the reducing agents are investigated through XPS, TGA, FT-IR, Raman and EA analysis. The degree of reduction of RGO depends on molecular structure of mercaptans and is controlled by the reaction time. The redox reaction is also employed to oxidize mercaptans into disulfides in medium to high yields under moderate conditions. The mechanism of the redox reaction may involve nucleophilic ring opening of oxirane on GO by alkylthio moiety, followed by addition of another alkylthio group, leaving the resulting disulfide. The reduction of the hydroxy group could be more complex, involving both radical and anionic processes.