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Register a new userPhoretic Interactions Generically Induce Dynamic Clusters and Wave Patterns in Active Colloids
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We introduce a representative minimal model for phoretically interacting active colloids. Combining kinetic theory, linear stability analyses, and a general relation between self-propulsion and phoretic interactions in auto-diffusiophoretic and auto-thermophoretic Janus colloids collapses the parameter space to two dimensions: area fraction and Peclet number. This collapse arises when the lifetime of the self-generated phoretic fields is not too short, and leads to a universal phase diagram showing that phoretic interactions {it generically} induce pattern formation in typical Janus colloids, even at very low density. The resulting patterns include waves and dynamic aggregates closely resembling the living clusters found in experiments on dilute suspension of Janus colloids.
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Despite a mounting evidence that the same gradients which active colloids use for swimming, induce important cross-interactions (phoretic interaction), they are still ignored in most many-body descriptions, perhaps to avoid complexity and a zoo of unknown parameters. Here we derive a simple model, which reduces phoretic far-field interactions to a pair-interaction whose strength is mainly controlled by one genuine parameter (swimming speed). The model suggests that phoretic interactions are generically important for autophoretic colloids (unless effective screening of the phoretic fields is strong) and should dominate over hydrodynamic interactions for the typical case of half-coating and moderately nonuniform surface mobilities. Unlike standard minimal models, but in accordance with canonical experiments, our model generically predicts dynamic clustering in active colloids at low density. This suggests that dynamic clustering can emerge from the interplay of screened phoretic attractions and active diffusion.
Because of consuming energy to drive their motion, systems of active colloids are intrinsically out of equilibrium. In the past decade, a variety of intriguing dynamic patterns have been observed in systems of active colloids, and they offer a new platform for studying non-equilibrium physics, in which computer simulation and analytical theory have played an important role. Here we review the recent progress in understanding the dynamic assembly of active colloids by using numerical and analytical tools. We review the progress in understanding the motility induced phase separation in the past decade, followed by the discussion on the effect of shape anisotropy and hydrodynamics on the dynamic assembly of active colloids.
The active motion of phoretic colloids leads them to accumulate at boundaries and interfaces. Such an excess accumulation, with respect to their passive counterparts, makes the dynamics of phoretic colloids particularly sensitive to the presence of boundaries and pave new routes to externally control their single particle as well as collective behavior. Here we review some recent theoretical results about the dynamics of phoretic colloids close to and adsorbed at fluid interfaces in particular highlighting similarities and differences with respect to solid-fluid interfaces.
Recent studies aimed at investigating artificial analogs of bacterial colonies have shown that low-density suspensions of self-propelled particles confined in two dimensions can assemble into finite aggregates that merge and split, but have a typical size that remains constant (living clusters). In this Letter we address the problem of the formation of living clusters and crystals of active particles in three dimensions. We study two systems: self-propelled particles interacting via a generic attractive potential and colloids that can move towards each other as a result of active agents (e.g. by molecular motors). In both cases fluid-like `living clusters form. We explain this general feature in terms of the balance between active forces and regression to thermodynamic equilibrium. This balance can be quantified in terms of a dimensionless number that allows us to collapse the observed clustering behaviour onto a universal curve. We also discuss how active motion affects the kinetics of crystal formation.
We consider the nonequilibrium dynamics of a charged active Brownian particle in the presence of a space dependent magnetic field. It has recently been shown that the Lorentz force induces a particle flux perpendicular to density gradients, thus preventing a diffusive description of the dynamics. Whereas a passive system will eventually relax to an equilibrium state, unaffected by the magnetic field, an active system subject to a spatially varying Lorentz force settles into a nonequilibrium steady state characterized by an inhomogeneous density and divergence-free bulk fluxes. A macroscopic flux of charged active particles is induced by the gradient of the magnetic field only and does not require additional symmetric breaking such as density or potential gradients. This stands in marked contrast to similar phenomena in condensed matter such as the classical Hall effect. In a confined geometry we observe circulating fluxes, which can be reversed by inverting the direction of the magnetic field. Our theoretical approach, based on coarse-graining of the Fokker-Planck equation, yields analytical results for the density, fluxes, and polarization in the steady state, all of which are validated by direct computer simulation. We demonstrate that passive tracer particles can be used to measure the essential effects of the Lorentz force on the active particle bath, and we discuss under which conditions the effects of the flux could be observed experimentally.
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