Asymmetric rectified electric and concentration fields in multicomponent electrolytes with surface reactions

TL;DR

This study reveals that electrochemical reactions can generate asymmetric rectified electric and concentration fields in multicomponent electrolytes, even with equal ionic diffusivities, advancing understanding of colloidal assembly and electrolyte transport.

Contribution

It introduces a theoretical framework for analyzing multicomponent electrolytes with surface reactions, showing electrochemical reactions alone can produce significant asymmetric rectified fields.

Findings

Electrochemical reactions can generate AREFs without diffusivity contrast.

AREFs induced by reactions can be stronger than those from diffusivity differences.

ARCFs support electrodiffusiophoresis in colloidal assembly.

Abstract

Recent studies have utilized AC fields and electrochemical reactions in multicomponent electrolyte solutions to control colloidal assembly. However, theoretical investigations have thus far been limited to binary electrolytes and have overlooked the impact of electrochemical reactions. In this study, we address these limitations by analyzing a system with multicomponent electrolytes, while also relaxing the assumption of ideally blocking electrodes to capture the effect of surface electrochemical reactions. Through a regular perturbation analysis in the low-applied-potential regime, we solve the Poisson-Nernst-Planck equations and obtain effective equations for electrical potential and ion concentrations. By employing a combination of numerical and analytical calculations, our analysis reveals a significant finding: electrochemical reactions alone can generate asymmetric rectified electric fields (AREFs), i.e., time-averaged, long-range electric fields, even when the diffusivities of the ionic species are equal. This finding expands our understanding beyond the conventional notion that AREFs arise solely from diffusivity contrast. Furthermore, we demonstrate that AREFs induced by electrochemical reactions can be stronger than those resulting from asymmetric diffusivities. Additionally, we report the emergence of asymmetric rectified concentration fields (ARCFs), i.e., time-averaged long-range concentration fields, which supports the electrodiffusiophoresis mechanism of colloidal assembly observed in experiments. We also derive analytical expressions for AREFs and ARCFs, emphasizing the role of imbalances in ionic strength and charge densities, respectively, as the driving forces behind their formation. The results presented in this article advance the field of colloidal assembly and also have implications for improved understanding of electrolyte transport in electrochemical devices.