Almog Yaniv, Yariv Ehud
Department of Mathematics, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
Phys Rev E Stat Nonlin Soft Matter Phys. 2011 Oct;84(4 Pt 1):041204. doi: 10.1103/PhysRevE.84.041204. Epub 2011 Oct 28.
Supporting-electrolyte solutions comprise chemically inert cations and anions, produced by salt dissolution, together with a reactive ionic species that may be consumed and generated on bounding ion-selective surfaces (e.g., electrodes or membranes). Upon application of an external voltage, a Faraday current is thereby established. It is natural to analyze this ternary-system process through a one-dimensional transport problem, employing the thin Debye-layer limit. Using a simple model of ideal ion-selective membranes, we have recently addressed this problem for moderate voltages [Yariv and Almog, Phys. Rev. Lett. 105, 176101 (2010)], predicting currents that scale as a fractional power of Debye thickness. We address herein the complementary problem of moderate currents. We employ matched asymptotic expansions, separately analyzing the two inner thin Debye layers adjacent to the ion-selective surfaces and the outer electroneutral region outside them. A straightforward calculation following comparable singular-perturbation analyses of binary systems is frustrated by the prediction of negative ionic concentrations near the cathode. Accompanying numerical simulations, performed for small values of Debye thickness, indicate a number unconventional features occurring at that region, such as inert-cation concentration amplification and electric-field intensification. The current-voltage correlation data of the electrochemical cell, obtained from compilation of these simulations, does not approach a limit as the Debye thickness vanishes. Resolution of these puzzles reveals a transformation of the asymptotic structure of the cathodic Debye layer. This reflects the emergence of an internal boundary layer, adjacent to the cathode, wherein field and concentration scaling differs from those of the Gouy-Chapman theory. The two-scale feature of the cathodic Debye layer is manifested through a logarithmic voltage scaling with Debye thickness. Accounting for this scaling, the complied current-voltage data collapses upon a single curve. This curve practically coincides with an asymptotically calculated universal current-voltage relation.
支持电解质溶液由盐溶解产生的化学惰性阳离子和阴离子以及一种反应性离子物种组成,该反应性离子物种可能在结合离子选择性表面(如电极或膜)上被消耗和生成。施加外部电压时,由此建立法拉第电流。通过一维输运问题,采用薄德拜层极限来分析这个三元系统过程是很自然的。使用理想离子选择性膜的简单模型,我们最近针对中等电压解决了这个问题[亚里夫和阿尔莫格,《物理评论快报》105,176101(2010)],预测电流与德拜厚度的分数幂成正比。我们在此解决中等电流的互补问题。我们采用匹配渐近展开,分别分析与离子选择性表面相邻的两个内部薄德拜层以及它们外部的外部电中性区域。对二元系统进行类似奇异摄动分析后的直接计算因预测阴极附近的负离子浓度为负而受阻。对小德拜厚度值进行的伴随数值模拟表明,在该区域出现了一些非常规特征,如惰性阳离子浓度放大和电场增强。从这些模拟结果汇编得到的电化学电池的电流 - 电压相关数据,在德拜厚度消失时并不趋近于一个极限。这些谜题的解决揭示了阴极德拜层渐近结构的转变。这反映了与阴极相邻的内部边界层的出现,其中场和浓度标度与古依 - 查普曼理论不同。阴极德拜层的双尺度特征通过与德拜厚度的对数电压标度表现出来。考虑到这种标度,汇编的电流 - 电压数据会汇聚到一条曲线上。这条曲线实际上与渐近计算的通用电流 - 电压关系重合。