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Doron Elad

Publications and source records attributed to Doron Elad.

2 recordsLinked to original sources

Finite domain effects in steady-state solutions of Poisson-Nernst-Planck equations

Steady-state solutions of the Poisson-Nernst-Planck model are studied in the asymptotic limit of large, but finite domains. By using asymptotic matching for integrals, we derive an approximate solution for the steady-state equation with exponentially small error with respect to the domain size. The approximation is used to quantify the extent of finite domain effects over the full parameter space. Surprisingly, already for small applied voltages (several thermal voltages), we found that finite domain effects are significant even for large domains (on the scale of hundreds of Debye lengths). Namely, the solution near the boundary, i.e., the boundary layer (electric double layer) structure, is sensitive to the domain size even when the domain size is many times larger than the characteristic width of the boundary layer. We focus on this intermediate regime between confined domains and `essentially infinite' domains, and study how the domain size effects the solution properties. We conclude by providing an outlook to higher dimensions with applications to ion channels and porous electrodes.

math.AP

From solvent free to dilute electrolytes: Essential components for a continuum theory

The increasing number of experimental observations on highly concentrated electrolytes and ionic liquids show qualitative features that are distinct from dilute or moderately concentrated electrolytes, such as self-assembly, multiple-time relaxation, and under-screening, which all impact the emergence of fluid/solid interfaces, and transport in these systems. Since these phenomena are not captured by existing mean field models of electrolytes, there is a paramount need for a continuum framework for highly concentrated electrolytes and ionic liquids. In this work, we present a self-consistent spatiotemporal framework for a ternary composition that comprises ions and solvent employing free energy that consists of short and long range interactions, together with a dissipation mechanism via Onsagers' relations. We show that the model can describe multiple bulk and interfacial morphologies at steady-state. Thus, the dynamic processes in the emergence of distinct morphologies become equally as important as the interactions that are specified in the equilibrium-free energy. The model equations not only provide insights to transport mechanisms beyond the Stokes-Einstein-Smoluchowski relations but also enables to qualitative recovery in the full range (three distinct regions) of non-monotonic electrical screening length that has been recently observed in experiments using organic solvent to dilute ionic liquids.

physics.chem-ph