Bromide adsorption on the three low-index faces of silver was investigated from mixed c mol dm -3 KBr + (0.02 - c) mol dm -3 KPF 6 solutions over a range of c from 1 × 10 -6 to 5 × 10 -3 mol dm -3 using the potential-step chronocoulometric technique. The adsorption behaviour on the Ag(110) face shows significant differences with respect to that on the Ag(111) and Ag(100) faces. Thus, the plot of the applied potential E vs. the specifically adsorbed charge density σ i of the bromide ions, for σ i equal and opposite to the charge density σ M on the metal, shows a rather abrupt decrease in slope with a decrease in σ i. Moreover, the plots of σ i vs. σ M at constant c intersect for σ i ≈ -35 μC cm -2. This behaviour is explained by a decrease in the negative value of the surface potential due to electron smoothing with an increase in |σ i| on Ag(110). The potential difference across the inner layer, once plotted against |σ i| at constant σ M, attains a maximum value before shifting linearly towards more negative values with a further increase in |σ i|; this behaviour, observed on all three low-index faces, is interpreted on the basis of a molecular model of the inner layer which accounts for the reorientation of the water dipoles and for the screening by the inhomogeneous electron gas.

Bromide electrosorption on the low-index faces of silver / M. Foresti; M. Innocenti; H. Kobayashi; G. Pezzatini; R. Guidelli.. - In: JOURNAL OF THE CHEMICAL SOCIETY. FARADAY TRANSACTIONS. - ISSN 0956-5000. - STAMPA. - 92 (20):(1996), pp. 3747-3756.

Bromide electrosorption on the low-index faces of silver

FORESTI, MARIA LUISA;INNOCENTI, MASSIMO;PEZZATINI, GIOVANNI;GUIDELLI, ROLANDO
1996

Abstract

Bromide adsorption on the three low-index faces of silver was investigated from mixed c mol dm -3 KBr + (0.02 - c) mol dm -3 KPF 6 solutions over a range of c from 1 × 10 -6 to 5 × 10 -3 mol dm -3 using the potential-step chronocoulometric technique. The adsorption behaviour on the Ag(110) face shows significant differences with respect to that on the Ag(111) and Ag(100) faces. Thus, the plot of the applied potential E vs. the specifically adsorbed charge density σ i of the bromide ions, for σ i equal and opposite to the charge density σ M on the metal, shows a rather abrupt decrease in slope with a decrease in σ i. Moreover, the plots of σ i vs. σ M at constant c intersect for σ i ≈ -35 μC cm -2. This behaviour is explained by a decrease in the negative value of the surface potential due to electron smoothing with an increase in |σ i| on Ag(110). The potential difference across the inner layer, once plotted against |σ i| at constant σ M, attains a maximum value before shifting linearly towards more negative values with a further increase in |σ i|; this behaviour, observed on all three low-index faces, is interpreted on the basis of a molecular model of the inner layer which accounts for the reorientation of the water dipoles and for the screening by the inhomogeneous electron gas.
1996
92 (20)
3747
3756
M. Foresti; M. Innocenti; H. Kobayashi; G. Pezzatini; R. Guidelli.
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Utilizza questo identificatore per citare o creare un link a questa risorsa: https://hdl.handle.net/2158/319894
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