电解质界面的非平衡稳定状态

M. Bier
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引用次数: 0

摘要

本研究利用泊松-奈恩斯特-普朗克(PNP)理论研究了以电流不等为特征的半离散准一维单价二元电解质溶液的非平衡稳态。得出了电场、电荷密度和数量密度的精确分析表达式,这些表达式取决于作为参数的电流密度。格拉哈姆方程的非平衡版本将单位横截面积的总空间电荷与相应的电势降贡献联系起来,由此推导出二重使用层的电流相关二重电容。在电流消失的极限下,这些结果与古伊-查普曼理论中的结果一致。研究表明,边界条件选择不当会导致 PNP 方程的非平衡稳态解出现负离子数密度。研究还提出了一个关于表面传导性构成关系的必要且适当的准则,可以检测出这种非物理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Non-equilibrium steady states of electrolyte interfaces
The non-equilibrium steady states of a semi-infinite quasi-one-dimensional univalent binary electrolyte solution, characterised by non-vanishing electric currents, are investigated by means of Poisson-Nernst-Planck (PNP) theory. Exact analytical expressions of the electric field, the charge density and the number density are derived, which depend on the electric current density as a parameter. From a non-equilibrium version of the Grahame equation, which relates the total space charge per cross-sectional area and the corresponding contribution of the electric potential drop, the current-dependent differential capacitance of the diffuse layer is derived. In the limit of vanishing electric current these results reduce to those within Gouy-Chapman theory. It is shown that improperly chosen boundary conditions lead to non-equilibrium steady state solutions of the PNP equations with negative ion number densities. A necessary and sufficient criterion on surface conductivity constitutive relations is formulated which allows one to detect such unphysical solutions.
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