Observation of gold electrode surface response to the adsorption and oxidation of thiocyanate in acidic electrolyte with broadband sum-frequency generation spectroscopy

被引:12
作者
Wang, Jingjing
Xu, Mei
Huangfu, Zhichao
Wang, Ying
He, Yuhan
Guo, Wei
Wang, Zhaohui [1 ]
机构
[1] Xiamen Univ, State Key Lab Phys Chem Solid Surfaces, MOE Key Lab Spectrochem Anal & Instrumentat, Coll Chem & Chem Engn, Xiamen 361005, Peoples R China
关键词
Nonlinear spectroscopy; Au electrode surface nonresonant response; Interface; Adsorption; Oxidation; IN-SITU; ENHANCED RAMAN; INFRARED-SPECTROSCOPY; POLYCRYSTALLINE AU; AQUEOUS-SOLUTIONS; IONIC LIQUID; TIO2; FILMS; PLATINUM; SFG; SILVER;
D O I
10.1016/j.vibspec.2016.04.001
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The adsorption and oxidation of thiocyanate (SCN-) on polycrystalline Au electrode surface in acidic electrolyte (10 mM NaSCN/0.1 M HClO4) have been investigated with broadband sum-frequency generation spectroscopy (BB-SFG). Potential-dependent behaviors of both the surface adsorbed species and the Au nonresonant (NR) electrode surface have been observed through BB-SFG band. A phase change of the S-bounded SCN-on the Au electrode surface occurs around 0.3 V in both the anodic (increase of surface potential) and cathodic (decrease of surface potential) sweeps. At surface potentials >0.7 V, oxidation and adsorption of the products (AuCN and Au(CN)(2)(-)) have been observed. Possible oxidation/reduction pathways have been discussed. The Stark slopes of the adsorbed SCN- SFG bands are significantly different in the anodic scan (before oxidation) from that in the cathodic scan (after the oxidation). The Au surface NR SFG band in the cathodic scan is much stronger than that in the anodic scan at the double layer surface potentials (-0.2 V to 0.5 V). The potential dependent Au surface NR BB-SFG band clearly shows that the adsorption/desorption and oxidation/reduction of surface species will affect the surface electronic structure. (C) 2016 Elsevier B.V. All rights reserved.
引用
收藏
页码:122 / 127
页数:6
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