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Register a new userSingle-file transport in periodic potentials: The Brownian asymmetric exclusion process
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Single-file Brownian motion in periodic structures is an important process in nature and technology, which becomes increasingly amenable for experimental investigation under controlled conditions. To explore and understand generic features of this motion, the Brownian asymmetric simple exclusion process (BASEP) was recently introduced. The BASEP refers to diffusion models, where hard spheres are driven by a constant drag force through a periodic potential. Here, we derive general properties of the rich collective dynamics in the BASEP. Average currents in the steady state change dramatically with the particle size and density. For an open system coupled to particle reservoirs, extremal current principles predict various nonequilibrium phases, which we verify by Brownian dynamics simulations. For general pair interactions we discuss connections to single-file transport by traveling-wave potentials and prove the impossibility of current reversals in systems driven by a constant drag and by traveling waves.
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We study the driven Brownian motion of hard rods in a one-dimensional cosine potential with an amplitude large compared to the thermal energy. In a closed system, we find surprising features of the steady-state current in dependence of the particle density. The form of the current-density relation changes greatly with the particle size and can exhibit both a local maximum and minimum. The changes are caused by an interplay of a barrier reduction, blocking and exchange symmetry effect. The latter leads to a current equal to that of non-interacting particles for a particle size commensurate with the period length of the cosine potential. For an open system coupled to particle reservoirs, we predict five different phases of non-equilibrium steady states to occur. Our results show that the particle size can be of crucial importance for non-equilibrium phase transitions in driven systems. Possible experiments for demonstrating our findings are pointed out.
Active particles may happen to be confined in channels so narrow that they cannot overtake each other (Single File conditions). This interesting situation reveals nontrivial physical features as a consequence of the strong inter-particle correlations developed in collective rearrangements. We consider a minimal model for active Brownian particles with the aim of studying the modifications introduced by activity with respect to the classical (passive) Single File picture. Depending on whether their motion is dominated by translational or rotational diffusion, we find that active Brownian particles in Single File may arrange into clusters which are continuously merging and splitting ({it active clusters}) or merely reproduce passive-motion paradigms, respectively. We show that activity convey to self-propelled particles a strategic advantage for trespassing narrow channels against external biases (e.g., the gravitational field).
We investigate the dynamics of a one-dimensional asymmetric exclusion process with Langmuir kinetics and a fluctuating wall. At the left boundary, particles are injected onto the lattice; from there, the particles hop to the right. Along the lattice, particles can adsorb or desorb, and the right boundary is defined by a wall particle. The confining wall particle has intrinsic forward and backward hopping, a net leftward drift, and cannot desorb. Performing Monte Carlo simulations and using a moving-frame finite segment approach coupled to mean field theory, we find the parameter regimes in which the wall acquires a steady state position. In other regimes, the wall will either drift to the left and fall off the lattice at the injection site, or drift indefinitely to the right. Our results are discussed in the context of non-equilibrium phases of the system, fluctuating boundary layers, and particle densities in the lab frame versus the frame of the fluctuating wall.
We revisit the totally asymmetric simple exclusion process with open boundaries (TASEP), focussing on the recent discovery by de Gier and Essler that the model has a dynamical transition along a nontrivial line in the phase diagram. This line coincides neither with any change in the steady-state properties of the TASEP, nor the corresponding line predicted by domain wall theory. We provide numerical evidence that the TASEP indeed has a dynamical transition along the de Gier-Essler line, finding that the most convincing evidence was obtained from Density Matrix Renormalisation Group (DMRG) calculations. By contrast, we find that the dynamical transition is rather hard to see in direct Monte Carlo simulations of the TASEP. We furthermore discuss in general terms scenarios that admit a distinction between static and dynamic phase behaviour.
We study the effects of an intermittent harmonic potential of strength $mu = mu_0 u$ -- that switches on and off stochastically at a constant rate $gamma$, on an overdamped Brownian particle with damping coefficient $ u$. This can be thought of as a realistic model for realisation of stochastic resetting. We show that this dynamics admits a stationary solution in all parameter regimes and compute the full time dependent variance for the position distribution and find the characteristic relaxation time. We find the exact non-equilibrium stationary state distributions in the limits -- (i) $gammallmu_0 $ which shows a non-trivial distribution, in addition as $mu_0toinfty$, we get back the result for resetting with refractory period; (ii) $gammaggmu_0$ where the particle relaxes to a Boltzmann distribution of an Ornstein-Uhlenbeck process with half the strength of the original potential and (iii) intermediate $gamma=2nmu_0$ for $n=1, 2$. The mean first passage time (MFPT) to find a target exhibits an optimisation with the switching rate, however unlike instantaneous resetting the MFPT does not diverge but reaches a stationary value at large rates. MFPT also shows similar behavior with respect to the potential strength. Our results can be verified in experiments on colloids using optical tweezers.
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