Coadsorption of sulfate anions and silver adatoms on the Au(111) single crystal electrode. Ex situ and in situ comparison

• Published in: Electrochimica acta 1995, Vol.40 (1), p.17-28
• Main Authors: Mrozek, Pawel, Sung, Yung-eun, Han, Moonsup, Gamboa-aldeco, Maria, Wieckowski, Andrzej, Chen, Chun-hsien, Gewirth, Andrew A.
• Format: Article
• Language: English
• Subjects: Chemistry; coadsorption; deposition; Electrochemistry; Electrodeposition; Exact sciences and technology; General and physical chemistry; silver; Study of interfaces; sulfate
• ISSN: 0013-4686; 1873-3859
• DOI: 10.1016/0013-4686(94)00249-Z

Interactions of sulfate anions in diluted sulfuric acid solutions with the Ag Au(111) surface were studied using Auger Electron Spectroscopy (AES), Low Energy Electron Diffraction (LEED), Atomic Force Microscopy (AFM), Core Electron Energy Loss Spectroscopy (CEELS) and electrochemistry. At electrode potentials more positive than those within the silver deposition range sulfate adsorbate forms an ordered Au(111)(√3 × √3)R30 ° adlattice, and gives rise to a corresponding, but diffuse, LEED pattern. Following extensive rinsing procedure, silver forms two well-ordered structures, Au(111)p(3 × 3) and Au(111)p(5 × 5). However, AFM images reveal a clear p(3 × 3)-4 Ag structure, which condenses to a close packed p(1 × 1)- Ag overlayer at more negative potentials. Distinctive S(LMM) Auger electron transitions and the S(L 2,3) core electron energy loss of the sulfate adsorbate show a characteristic S 6+ sulfur valency, giving evidence that the sulfur oxidation state is not altered in the ultra-high vacuum environment following solution/vacuum transfer.