In-Situ STM Visualization of Molecular Structural Evolution during Electrochemical Oxidation Coupling of Para-Aminothiophenol on Au(111)
Zi-Wei Ma , Tai-Rui Wu , An-Ni Zheng , Lai-Ke Chen , Yuan-Hui Xiao , Zhao-Bin Chen , Qing-Na Zheng , Jian-Zhang Zhou , Jia-Wei Yan , De-Yin Wu
Journal of Electrochemistry ›› 2026, Vol. 32 ›› Issue (7) : 2603031
Para-aminothiophenol (PATP) is not only a widely-used probe molecule in the field of surface-enhanced Raman spectroscopy (SERS), but also an important model molecule for interfacial reactions, exhibiting distinct photo- and electro-oxidation pathways, so that PATP is selectively activated under different external fields. The evolution of products and intermediates during electrochemical oxidative coupling remains unknown. In this study, we have investigated the dynamic electrochemical oxidation process of PATP on the Au(111) surface using cyclic voltammetry, electrochemical (EC)-SERS, and in situ electrochemical scanning tunneling microscopy (EC-STM). The results showed that PATP forms an unsaturated adsorption coverage on Au(111) in an acidic solution. When the potential was positively shifted to the oxidation potential range, the cation radical generated by PATP oxidation alternated with PATP molecules in arrangement. Once the coupling reaction occurred, the adsorption structure of alternating arrangement was transformed into the stripe structure as observed in the STM images. Finally, the coverage on the Au(111) surface decreased and a
In situ electrochemical scanning tunneling microscopy / Para-aminothiophenol (PATP) / 4'-mereapto-N-phenylquinone diimine / Electrochemical surface-enhanced Raman spectroscopy
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