Self-chemophoresis in the thin diffuse interface approximation
Alvaro Dom\'inguez, Mihail N. Popescu

TL;DR
This paper critically examines the theoretical framework of self-chemophoresis in colloidal particles, focusing on the thin diffuse interface approximation and exploring how simplifying assumptions affect predicted particle motion.
Contribution
It provides a detailed analysis of the thin-layer and lubrication approximations in the self-chemophoresis model, offering insights into their validity and potential relaxations.
Findings
Re-examination of the integral representation of particle motion.
Identification of key assumptions in the thin-layer and lubrication approximations.
Discussion on how relaxing these approximations impacts particle dynamics.
Abstract
Self-chemophoresis is an appealing and quite successful interpretation of the motility exhibited by certain chemically active colloidal particles suspended in a solution of their "fuel": the particle has a phoretic response to self-generated, rather than externally imposed, inhomogeneities in the chemical composition of the solution. The postulated mechanism of chemophoresis is the interaction of the particle (via an adsorption potential) with the chemical inhomogeneities in the surrounding medium. When the range of this interaction is much smaller than any other relevant scale in the system, the (translational and rotational) phoretic velocities can be described in terms of a phoretic coefficient and a slip fluid velocity at the surface of the particle. Using the case of a spherical particle as a simple and physically insightful example, here we exploit an integral representation of…
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Taxonomy
TopicsField-Flow Fractionation Techniques · Material Dynamics and Properties · nanoparticles nucleation surface interactions
