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Ritu R. Raj

Publications and source records attributed to Ritu R. Raj.

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Rethinking Balance Sheets: A Poisson-Nernst-Planck Based Approach for Modeling Concentration and Flux Profiles Inside an Electrochemical Cell

Electrochemical cells serve as a building block for producing and storing electrical energy from chemical reactions. The analysis of ion transport in these systems forms the foundation for understanding more complex electrochemical systems that are becoming increasingly present in the broader societal energy infrastructure. From a pedagogical perspective, the ``balance sheets" introduced in Chapter 4 of Electrochemical Methods: Fundamentals and Applications by Alan J. Bard, Larry R. Faulkner and Henry S. White (hereafter referred to as BFW) provides a first-pass approach to analyze ion transport in electrochemical cells. However, the balance sheet approach lacks first-principles justifications from the underlying equations that describe the transport processes in electrochemical cells. In this work, we compare a first-principles approach via the Poisson-Nernst-Planck equations to describe ion transport in electrochemical cells to that of the balance sheet approach. By re-working the examples presented in BFW, we illustrate that the balance sheet approach is only valid in limited scenarios. Furthermore, we show that the PNP equations provide a more physical route to analyze ion transport in electrochemical systems. We hope the approach outlined here will be adopted by electrochemical engineering researchers and instructors.

physics.chem-ph

Two-dimensional diffusiophoretic colloidal banding: Optimizing the spatial and temporal design of solute sinks and sources

In this work, we numerically investigate the impact of two-dimensional solute gradients on the distribution of colloidal particles, i.e., colloidal banding, induced via diffusiophoresis. The solute gradients are generated by spatially arranged sources and sinks that emit/absorb a time-dependent solute flux. First we study a dipole system, i.e., one source and one sink, and discover that interdipole diffusion and flux decay timescales dictate colloidal banding. At timescales shorter than the interdipole diffusion timescale, we observe a rapid enhancement in particle enrichment around the source due to repulsion from the sink. However, at timescales longer than the interdipole diffusion timescale, the source and sink screen each other, leading to a slower enhancement. If the solute flux decays at the timescale of interdipole diffusion, an optimal separation distance is obtained such that particle enrichment is maximized. We find that the partition coefficient between solute inside the source and the bulk strongly impacts the optimal separation distance. Surprisingly, the diffusivity ratio between solute in the source and bulk has a much weaker impact on the optimal dipole separation distance. We also examine an octupole configuration, i.e., four sinks and four sources, arranged in a circle, and demonstrate that the geometric arrangement that maximizes enrichment depends on the radius of the circle. If the radius of the circle is small, it is preferred to have sources and sinks arranged in an alternating fashion. However, if the radius of the circle is large, a consecutive arrangement of sources and sinks is optimal. Our numerical framework introduces a novel method for spatially and temporally designing the banded structure of colloidal particles in two dimensions using diffusiophoresis and opens up new avenues in a field that has primarily focused on one-dimensional solute gradients.

cond-mat.soft