Electrochemical and FTIR studies of 4-cyanopyridine adsorption at the gold(111) | solution interface

被引:29
作者
Chen, AC [1 ]
Yang, DF [1 ]
Lipkowski, J [1 ]
机构
[1] Univ Guelph, Guelph Waterloo Ctr Grad Work Chem, Guelph, ON N1G 2W1, Canada
基金
加拿大自然科学与工程研究理事会;
关键词
adsorption at Au(111); 4-cyanopyridine; in-situ reflection IR spectroscopy;
D O I
10.1016/S0022-0728(99)00338-1
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Subtractively normalized interfacial Fourier transform infrared spectroscopy (SNIFTIRS) has been employed to study the adsorption of 4-cyanopyridine (4-CNPy) at the Au(111) electrode surface. The vibrational spectra have been used to study the character of surface coordination and the stability of adsorbed 4-CNPy molecules. Our studies show that 4-CNPy molecules are totally desorbed from the Au(111) surface at potentials lower than -0.7 V versus SCE and that they adsorb at the gold surface at more positive potentials. At potentials lower than 0.05 V versus SCE, the adsorption has a non-dissociative character. The 4-CNPy molecules are initially oriented flat (pi-bonded) on the electrode surface and reorient from the flat to a vertical State when the electrode potential approaches 0 V (SCE). When the potential is greater than 0.05 V versus SCE, the character of 4-CNPy adsorption becomes dissociative and the adsorbed molecules partially hydrolyze to form isonicotinamide (INA). The IR spectra acquired at very positive potentials indicate that 4-CNPy is oxidized at E > 0.6 V versus SCE. (C) 1999 Elsevier Science S.A. All rights reserved.
引用
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页码:130 / 138
页数:9
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