Adsorption of Au-containing species and heterogeneous isotope exchange of Au atoms at the Au electrode|dicyanoaurate solution interface

被引:0
作者
Poskus, D [1 ]
Agafonovas, G [1 ]
机构
[1] Inst Chem, LT-2600 Vilnius, Lithuania
来源
JOURNAL OF ELECTROANALYTICAL CHEMISTRY | 1998年 / 457卷 / 1-2期
关键词
adsorption; dicyanoaurate; gold; heterogeneous isotope exchange; radiotracer method;
D O I
10.1016/S0022-0728(98)00280-0
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Both the adsorption of Au-containing species on a polycrystalline gold electrode in alkaline 10(-4) M dicyanoaurate solution and the heterogeneous isotope exchange of Au atoms in this system were studied by the use of 'electrode lowering' radiotracer techniques and Au-195-labelled dicyanoaurate. At an electrode potential of 0.1 V (SHE), the rate of adsorption of Au-containing species is considerably higher than that of heterogeneous isotope exchange which makes it possible to discriminate the contribution of adsorption from that of heterogeneous isotope exchange. The surface concentration of Au-containing species adsorbed on the gold electrode at 0.1 V determined in this study is close to that of CN-containing species adsorbed in the same system obtained previously [1]. The results obtained suggest strongly that AuCN species are adsorbed on a gold electrode from alkaline dicyanoaurate solutions and the heterogeneous isotope exchange is confined to the atomic monolayer of gold. The rate of heterogeneous isotope exchange at 0.1 V is some orders of magnitude higher than the partial cathodic current density extrapolated to this potential. (C) 1998 Elsevier Science S.A. All rights reserved.
引用
收藏
页码:171 / 176
页数:6
相关论文
共 25 条
[1]   ON THE POTENTIAL DEPENDENCE OF THE CN STRETCH FREQUENCY ON AU ELECTRODES STUDIED BY SERS [J].
BALTRUSCHAT, H ;
HEITBAUM, J .
JOURNAL OF ELECTROANALYTICAL CHEMISTRY, 1983, 157 (02) :319-326
[2]  
BEK RY, 1996, ELEKTROKHIMIYA, V32, P1448
[3]  
BEK RY, 1987, IZV SIB OTD AKAD NAU, V5, P27
[4]  
GERISCHER H, 1954, Z ELEKTROCHEM BER BU, V59, P819
[5]  
HAISSINSKY M, 1961, NUCL CHEM ITS APPL, P747
[6]  
HEYFETZ VL, 1959, ZH PRIKL KHIM, V32, P1781
[7]  
HURLEN T, 1963, ELECTROCHIM ACTA, V8, P741
[8]  
KAZARINOV VE, 1975, ELEKTROKHIMIYA, V11, P1482
[9]  
KAZARINOV VE, 1974, ELEKTROKHIMIYA, V10, P1736
[10]  
KAZARINOV VE, 1974, ELEKTROKHIMIYA, V10, P196