Spontaneously Formed Sulfur Adlayers on Gold in Electrolyte Solutions: Adsorbed Sulfur or Gold Sulfide?

P.G. LUSTEMBERG; C. VERICAT; G. A. BENITEZ; M.E. VELA; N. G. TOGNALLI; A. FAINSTEIN; M.L. MARTIARENA; R.C. SALVAREZZA

JOURNAL OF PHYSICAL CHEMISTRY C

American Chemical Society

Lugar: Washington D.C.; Año: 2008 vol. 112 p. 11394 - 11402

1932-7447

High coverage S phases (surface coverage g0.33), spontaneously formed by immersion of Au(111) in Na2S aqueous solutions at room temperature, have been studied by scanning tunneling microscopy (STM), X-ray photoelectron spectroscopy (XPS), surface enhanced Raman spectroscopy (SERS), electrochemistry, and density functional theory (DFT) calculations. XPS data show no evidence of a AuS phase, as no oxidized gold is detected. Voltammetric data are also inconsistent with the formation of a AuS phase with 0.5 stoichiometry.In situ and ex situ SERS measurements of S-covered nanostructured gold substrates demonstrate that the surface species present at the gold surface consist of a mixture of chemisorbed S and polysulfide species, as already proposed based on in situ STM images. A DFT surface model that is energetically feasible and reproduces well the experimental STM images is presented. The proposed model involves only a small rearrangement of the upper Au layer and coexistence of monomeric and polymeric S. Therefore, the high coverage S phase should be described as a mixture of monomeric and polymeric chemisorbed sulfur rather than as an extended 2D AuS phase.