Adsorption of adipic acid conjugates at the Au(1 1 1) electrode|aqueous solution interface

被引:3
作者
Doneux, Th [1 ,2 ]
Nichols, R. J. [2 ]
机构
[1] Univ Libre Bruxelles, Fac Sci, B-1050 Brussels, Belgium
[2] Univ Liverpool, Dept Chem, Liverpool L69 7ZD, Merseyside, England
关键词
Single crystal; Chronocoulometry; Anion adsorption; Adipic acid; Phase transition; Adsorption free energy; SCANNING-TUNNELING-MICROSCOPY; CONSTANT CATIONIC STRENGTH; SELF-ASSEMBLED MONOLAYERS; THIN-FILM ELECTRODES; GOLD SINGLE-CRYSTAL; INFRARED-SPECTROSCOPY; DICARBOXYLIC IONS; SURFACES; SULFATE; SPECTRA;
D O I
10.1016/j.jelechem.2010.02.003
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
The adsorption of adipic acid an aliphatic dicarboxylic acid has been studied at the Au(1 1 1) electrode vertical bar aqueous solution interface by cyclic voltammetry chronocoulometry and in situ infrared spectroscopy The voltammograms recorded at different pH values in adipic acid biadipate and adipate solutions point to the adsorption of anionic species A potential dependent order-disorder phase transition is apparent from the voltammetric curves the transition potential being directly influenced by the solution pH From infrared spectra it is concluded that as the electrode potential is made more positive the amount of carboxylic groups in the adsorbed layer increases The maximum surface excess concentration G = (4 4 +/- 0 6) x 10(-10) mol cm(-2) and the adsorption free energy -Delta(ads)G = 125-190 kJ mol(-1) have been determined by a thermodynamic analysis of the chronocoulometric data (C) 2010 Elsevier B V All rights reserved
引用
收藏
页码:95 / 101
页数:7
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