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Autores principales: Diaz, Javier, Pagonabarraga, Ignacio, Calero, Carles
Formato: Preprint
Publicado: 2025
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Acceso en línea:https://arxiv.org/abs/2510.06163
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author Diaz, Javier
Pagonabarraga, Ignacio
Calero, Carles
author_facet Diaz, Javier
Pagonabarraga, Ignacio
Calero, Carles
contents Propulsion of colloidal particles due to momentum transfer from localized surface reactions is investigated by solving the exact unsteady Stokes equation. We model the effect of surface reactions as either a {\it force dipole} acting on the fluid or a {\it pair force} acting on both the colloid and the fluid. Our analysis reveals that after a single reaction event the colloid's velocity initially decays as $\sim t^{-1/2}$, followed by a long-time tail decay $\sim t^{-5/2}$. This behavior is distinct from the $\sim t^{-3/2}$ decay seen for simple impulsively forced particles, a result of the force-free nature of the reaction mechanism. The velocity and transient dynamics are strongly controlled by the distance of the reaction from the colloid surface. For a colloid subject to periodic reactions, the theory predicts a steady-state velocity that is comparable to experimental results and previous simulations, suggesting that direct momentum transfer is a relevant mechanism for self-propulsion in systems like Janus particles. Finally, our study shows that fluid compressibility is not required for momentum transfer to produce colloidal propulsion.
format Preprint
id arxiv_https___arxiv_org_abs_2510_06163
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Hydrodynamic Mechanism of Colloidal Propulsion through Momentum Exchange
Diaz, Javier
Pagonabarraga, Ignacio
Calero, Carles
Soft Condensed Matter
Propulsion of colloidal particles due to momentum transfer from localized surface reactions is investigated by solving the exact unsteady Stokes equation. We model the effect of surface reactions as either a {\it force dipole} acting on the fluid or a {\it pair force} acting on both the colloid and the fluid. Our analysis reveals that after a single reaction event the colloid's velocity initially decays as $\sim t^{-1/2}$, followed by a long-time tail decay $\sim t^{-5/2}$. This behavior is distinct from the $\sim t^{-3/2}$ decay seen for simple impulsively forced particles, a result of the force-free nature of the reaction mechanism. The velocity and transient dynamics are strongly controlled by the distance of the reaction from the colloid surface. For a colloid subject to periodic reactions, the theory predicts a steady-state velocity that is comparable to experimental results and previous simulations, suggesting that direct momentum transfer is a relevant mechanism for self-propulsion in systems like Janus particles. Finally, our study shows that fluid compressibility is not required for momentum transfer to produce colloidal propulsion.
title Hydrodynamic Mechanism of Colloidal Propulsion through Momentum Exchange
topic Soft Condensed Matter
url https://arxiv.org/abs/2510.06163