Abstract

The stoichiometry and reaction mechanism of Pt deposition via surface limited redox replacement (SLRR) of Cu underpotential-deposited (UPD) monolayer on Au(111) was studied using in situ polarization dependent total reflection fluorescence X-ray absorption fine structure (PTRF-XAFS), scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), and cyclic voltammetry (CV). We proposed that Pt deposition via SLRR of Cu UPD monolayer leads to formation/deposition of Pt-surface species mainly consisting of Pt(II) chloride with a square planar local structure [PtCl4] parallel to the Au surface (60%) which has a strong interaction of the Pt complex with the Au substrate. The rest (40%) was one-monolayer Pt metal cluster. This result provides a new understanding into the mechanism and stoichiometry of the SLRR reaction, which has a wide application for synthesis of monolayer catalysts.

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