Excess nonspecific Coulomb ion adsorption at the metal electrode/electrolyte solution interface: Role of the surface layer

A. M. Gabovich, Yu. A. Reznikov, and A. I. Voitenko
Phys. Rev. E 73, 021606 – Published 27 February 2006

Abstract

Excess ion adsorption Γ induced by the polarization image forces in the system of a metal electrode/symmetric electrolyte solution separated by an insulating interlayer has been calculated. The adopted theoretical scheme involves the Coulomb Green’s function in a three-layer system with sharp interfaces and specular reflection at them. The influence of the spatial dispersion of the dielectric permittivities εi(k) in all the three media on the image force energy Wim and the adsorption Γ has been analyzed, where k is the wave vector. A comparison with the classical model, where εi=const, has been carried out. It has been shown that both the Debye-Hückel ion screening and the spatial dispersion of the solvent contribution εsolv(k) to the overall dielectric function εel(k) of the electrolyte solution lead to the qualitative difference with the results for the classical model. In particular, in a wide range of ion concentrations n0 a thin interlayer L510Å effectively screens out the attractive influence of the metallic electrode, so that the net Coulomb adsorption may become repulsive. The approach and the results obtained qualitatively describe two physically different situations. Specifically, the introduced interlayer corresponds either to the dense near-electrode (inner) electrolyte layer or to the intentionally deposited control coating of arbitrary thickness.

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  • Received 5 October 2005

DOI:https://doi.org/10.1103/PhysRevE.73.021606

©2006 American Physical Society

Authors & Affiliations

A. M. Gabovich, Yu. A. Reznikov, and A. I. Voitenko*

  • Institute of Physics, National Academy of Sciences of Ukraine, 46 Nauka Ave., Kyiv 03028, Ukraine

  • *Electronic address: collphen@iop.kiev.ua

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Issue

Vol. 73, Iss. 2 — February 2006

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