No Arabic abstract
Self-propelled colloids constitute an important class of intrinsically non-equilibrium matter. Typically, such a particle moves ballistically at short times, but eventually changes its orientation, and displays random-walk behavior in the long-time limit. Theory predicts that if the velocity of non-interacting swimmers varies spatially in 1D, $v(x)$, then their density $rho(x)$ satisfies $rho(x) = rho(0)v(0)/v(x)$, where $x = 0$ is an arbitrary reference point. Such a dependence of steady-state $rho(x)$ on the particle dynamics, which was the qualitative basis of recent work demonstrating how to `paint with bacteria, is forbidden in thermal equilibrium. We verify this prediction quantitatively by constructing bacteria that swim with an intensity-dependent speed when illuminated. A spatial light pattern therefore creates a speed profile, along which we find that, indeed, $rho(x)v(x) = mathrm{constant}$, provided that steady state is reached.
In a microrheological set-up a single probe particle immersed in a complex fluid is exposed to a strong external force driving the system out of equilibrium. Here, we elaborate analytically the time-dependent response of a probe particle in a dilute suspension of Brownian particles to a large step-force, exact in first order of the density of the bath particles. The time-dependent drift velocity approaches its stationary state value exponentially fast for arbitrarily small driving in striking contrast to the power-law prediction of linear response encoded in the long-time tails of the velocity autocorrelation function. We show that the stationary-state behavior depends nonanalytically on the driving force and connect this behavior to the persistent correlations in the equilibrium state. We argue that this relation holds generically. Furthermore, we elaborate that the fluctuations in the direction of the force display transient superdiffusive behavior.
We derive equations of motion for the mean-squared displacement (MSD) of an active Brownian particle (ABP) in a crowded environment modeled by a dense system of passive Brownian particles, and of a passive tracer particle in a dense active-Brownian particle system, using a projection-operator scheme. The interaction of the tracer particle with the dense host environment gives rise to strong memory effects. Evaluating these approximately in the framework of a recently developed mode-coupling theory for the glass transition in active Brownian particles (ABP-MCT), we discuss the various regimes of activity-induced super-diffusive motion and density-induced sub-diffusive motion. The predictions of the theory are shown to be in good agreement with results from an event-driven Brownian dynamics simulation scheme for the dynamics of two-dimensional active Brownian hard disks.
We develop efficient numerical methods for performing many-body Brownian dynamics simulations of a recently-observed fingering instability in an active suspension of colloidal rollers sedimented above a wall [M. Driscoll, B. Delmotte, M. Youssef, S. Sacanna, A. Donev and P. Chaikin, Nature Physics, 2016, doi:10.1038/nphys3970]. We present a stochastic Adams-Bashforth integrator for the equations of Brownian dynamics, which has the same cost as but is more accurate than the widely-used Euler-Maruyama scheme, and uses a random finite difference to capture the stochastic drift proportional to the divergence of the configuration-dependent mobility matrix. We generate the Brownian increments using a Krylov method, and show that for particles confined to remain in the vicinity of a no-slip wall by gravity or active flows the number of iterations is independent of the number of particles. Our numerical experiments with active rollers show that the thermal fluctuations set the characteristic height of the colloids above the wall, both in the initial condition and the subsequent evolution dominated by active flows. The characteristic height in turn controls the timescale and wavelength for the development of the fingering instability.
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 investigate velocity probability distribution functions (PDF) of sheared hard-sphere suspensions. As observed in our Stokes flow simulations and explained by our single-particle theory, these PDFs can show pronounced deviations from a Maxwell-Boltzmann distribution. The PDFs are symmetric around zero velocity and show a Gaussian core and exponential tails over more than six orders of magnitude of probability. Following the excellent agreement of our theory and simulation data, we demonstrate that the distribution functions scale with the shear rate, the particle volume concentration, as well as the fluid viscosity.