CRYSTAL-FACE EFFECTS ON ADSORPTION OF IONIC AND NONIONIC SPECIES ON AG ELECTRODES - AN ELECTROCHEMICAL AND STM STUDY

被引:52
作者
FORESTI, ML [1 ]
ALOISI, G [1 ]
INNOCENTI, M [1 ]
KOBAYASHI, H [1 ]
GUIDELLI, R [1 ]
机构
[1] UNIV FLORENCE,DEPT CHEM,I-50121 FLORENCE,ITALY
关键词
ADSORPTION ISOTHERMS; CHEMISORPTION; LOW INDEX SINGLE CRYSTAL SURFACES; SCANNING TUNNELING MICROSCOPY; SILVER;
D O I
10.1016/0039-6028(95)00423-8
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The behaviour of the low-index faces of silver towards specific adsorption from aqueous solutions was investigated by measuring the adsorption of n-hexanol and tert-pentanol, which exemplifies the behaviour of physisorbed neutral compounds, the adsorption of bromide ions, which exemplifies the behaviour of chemisorbed ions, and the adsorption of uracil. STM images of specifically adsorbed bromide and iodide ions on Ag(111) were determined. The increase in the adsorptivity of the two aliphatic alcohols in the order Ag(110)< Ag(100)< Ag(111), i.e. in the order of decreasing hydrophilicity, is justified on the basis of a model of the Ag/electrolyte interface. The increase in the dipole moment associated with the adsorption of one bromide ion in the order Ag(111) <Ag(100) <Ag(110) is explained by a model of the adsorbed monolayer. The adsorption of uracil on Ag(111) is shown to proceed by diffusion control according to a Frumkin isotherm, followed by the nucleation and growth of a condensed two-dimensional phase.
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页码:241 / 251
页数:11
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