Chloride and iodide electrosorption on Ag(1 1 1)

被引:5
作者
Foresti, Maria Luisa [1 ]
Innocenti, Massimo [1 ]
Loglio, Francesca [1 ]
Becucci, Lucia [1 ]
Guidelli, Rolando [1 ]
机构
[1] Univ Florence, Dept Chem, I-50019 Florence, Italy
关键词
Partial charge transfer; Chronocoulometry; Single crystal electrodes; Electrosorption valency; ELECTROCHEMICAL DESORPTION; ADSORPTION BEHAVIOR; SOLUTION INTERFACE; DOUBLE-LAYER; MERCURY; ELECTRODES; MONOLAYERS; CHARGE; SURFACES; SILVER;
D O I
10.1016/j.jelechem.2010.02.002
中图分类号
O65 [分析化学];
学科分类号
070302 ; 081704 ;
摘要
Chloride and iodide adsorption on Ag(1 1 1) was investigated from mixed c M KX + (0 02 - c) M KPF(6) with X = Cl I using the potential-step chronocoulometric technique Measurements were carried out at potentials negative of -05 V/SCE where STM does not provide images of ordered adlayers of these halides Their adsorption behavior was compared with that of bromide ion on Ag(1 1 1) reported in a previous work The plot of the applied potential E decreased by the potential difference phi(d) across the diffuse layer shows a maximum when plotted against the specifically adsorbed charge density sigma(1) of the halides at constant charge density sigma(M) on the metal This behavior is explained by an appreciable contribution from reorientation and displacement of adsorbed water molecules by the adsorbing halides The mini mum of the E - phi(d) V(S) sigma(1) plot is much shallower for iodide than for chloride and bromide The sigma(1), VS log c plots at sigma(M) = 0 are linear thus satisfying the Temkin isotherm The resulting interaction factor is appreciably less repulsive for iodide than for chloride and bromide These results indicate that partial charge transfer from iodide to Ag(1 1 1) is appreciable even at negative potentials at which adsorption is random as distinct from chloride and bromide (C) 2010 Elsevier B V All rights reserved
引用
收藏
页码:89 / 94
页数:6
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