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A new continuum perspective for phoretic motion is developed that is applicable to particles of any shape in ‘microstructured’ fluids such as a suspension of solute or bath particles. Using the reciprocal theorem for Stokes flow it is shown that the local osmotic pressure of the solute adjacent to the phoretic particle generates a thrust force (via a ‘slip’ velocity) which is balanced by the hydrodynamic drag such that there is no net force on the body. For a suspension of passive Brownian bath particles this perspective recovers the classical result for the phoretic velocity owing to an imposed concentration gradient. In a bath of active particles that self-propel with characteristic speed $$U_0$$ for a time $$\tau _R$$ and then change direction randomly, taking a step of size $$\ell = U_0 \tau _R$$ , at high activity the phoretic velocity is $$\boldsymbol {U} \sim - U_0 \ell \boldsymbol {\nabla } \phi _b$$ , where $$\phi _b$$ is a measure of the ‘volume’ fraction of the active bath particles. The phoretic velocity is independent of the size of the phoretic particle and of the viscosity of the suspending fluid. Because active systems are inherently out of equilibrium, phoretic motion can occur even without an imposed concentration gradient. It is shown that at high activity when the run length varies spatially, net phoretic motion results in $$\boldsymbol {U} \sim - \phi _b U_0 \boldsymbol {\nabla } \ell$$ . These two behaviours are special cases of the more general result that phoretic motion arises from a gradient in the swim pressure of active matter. Finally, it is shown that a field that orients (but does not propel) the active particles results in a phoretic velocity $$\boldsymbol {U} \sim - \phi _b U_0 \ell \boldsymbol {\nabla }\varPsi$$ , where $$\varPsi$$ is the (non-dimensional) potential associated with the field.
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Unified mobility expressions for externally driven and self-phoretic propulsion of particles
The mobility of externally driven phoretic propulsion of particles is evaluated by simultaneously solving the solute conservation equation, interaction potential equation and the modified Stokes equation. While accurate, this approach is cumbersome, especially when the interaction potential decays slowly compared with the particle size. In contrast to external phoresis, the motion of self-phoretic particles is typically estimated by relating the translation and rotation velocities with the local slip velocity. While this approach is convenient and thus widely used, it is only valid when the interaction decay length is significantly smaller than the particle size. Here, by taking inspiration from Brady (J. Fluid Mech., vol. 922, 2021, A10), which combines the benefits of two approaches, we reproduce their unified mobility expressions with arbitrary interaction potentials and show that these expressions can conveniently recover the well-known mobility relationships of external electrophoresis and diffusiophoresis for arbitrary double-layer thickness. Additionally, we show that for a spherical microswimmer, the derived expressions relax to the slip velocity calculations in the limit of the thin interaction length scales. We also employ the derived mobility expressions to calculate the velocities of an autophoretic Janus particle. We find that there is significant dampening in the translation velocity even when the interaction length is an order of magnitude larger than the particle size. Finally, we study the motion of a catalytically self-propelled particle, while it also propels due to external concentration gradients, and demonstrate how the two propulsion modes compete with each other.
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- Award ID(s):
- 2238412
- PAR ID:
- 10566440
- Publisher / Repository:
- Cambridge University Press
- Date Published:
- Journal Name:
- Journal of Fluid Mechanics
- Volume:
- 994
- ISSN:
- 0022-1120
- Format(s):
- Medium: X
- Sponsoring Org:
- National Science Foundation
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- Free Publicly Accessible Full Text
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Accepted Manuscript1.0
- Journal Article:
- https://doi.org/10.1017/jfm.2024.588
