Publications by authors named "Punyabrata Pradhan"

Characterizing current fluctuations in a steady state is of fundamental interest and has attracted considerable attention in the recent past. However, the bulk of the studies are limited to systems that either do not exhibit a phase transition or are far from criticality. Here we consider a symmetric zero-range process on a ring that is known to show a phase transition in the steady state.

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We study the Oslo model, a paradigm for absorbing-phase transition, on a one-dimensional ring of L sites with a fixed global density ρ[over ¯]; we consider the system strictly above critical density ρ_{c}. Notably, microscopic dynamics conserve both mass and center of mass (CoM), but lack time-reversal symmetry. We show that, despite having highly constrained dynamics due to CoM conservation, the system exhibits diffusive relaxation away from criticality and superdiffusive relaxation near criticality.

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Article Synopsis
  • This study examines current fluctuations in two models of hardcore run-and-tumble particles (RTPs) on a one-dimensional lattice, focusing on how these fluctuations behave over time for various densities and tumbling rates.
  • The research shows that the cumulative current fluctuations grow differently over time; they first increase subdiffusively and later transition to a linear (diffusive) growth as time progresses.
  • The authors establish universal scaling laws for current fluctuations across both models, revealing consistent behavior in the limits of low density and tumbling rate, and validating their theoretical findings with simulations.
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Article Synopsis
  • The study investigates the bulk-diffusion coefficient \( D(\rho, \gamma) \) for hardcore run-and-tumble particles on a periodic lattice, examining two models: the standard hardcore model (Model I) and a long-ranged lattice gas variant (Model II).
  • It finds that the diffusion coefficient varies with density in a nonlinear way, transitioning from \( \alpha=2 \) at high densities to \( \alpha=0 \) at low densities, indicating complex interactions between particle persistence and density.
  • The results lead to a scaling relationship for \( D \) as the density and tumbling rate approach zero, which holds across different dimensions and particle interactions.
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We consider a one-dimensional lattice gas model of hardcore particles with nearest-neighbor interaction in presence of a time-periodic external potential. We investigate how attractive or repulsive interaction affects particle transport and determine the conditions for optimum transport, i.e.

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We study dynamic correlations for current and mass, as well as the associated power spectra, in the one-dimensional conserved Manna sandpile. We show that, in the thermodynamic limit, the variance of cumulative bond current up to time T grows subdiffusively as T^{1/2-μ} with the exponent μ≥0 depending on the density regimes considered and, likewise, the power spectra of current and mass at low frequency f varies as f^{1/2+μ} and f^{-3/2+μ}, respectively. Our theory predicts that, far from criticality, μ=0 and, near criticality, μ=(β+1)/2ν_{⊥}z>0 with β, ν_{⊥}, and z being the order parameter, correlation length, and dynamic exponents, respectively.

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We calculate the bulk-diffusion coefficient and the conductivity in nonequilibrium conserved-mass aggregation processes on a ring. These processes involve chipping and fragmentation of masses, which diffuse on a lattice and aggregate with their neighboring masses on contact, and, under certain conditions, they exhibit a condensation transition. We find that, even in the absence of microscopic time reversibility, the systems satisfy an Einstein relation, which connects the ratio of the conductivity and the bulk-diffusion coefficient to mass fluctuation.

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We study relaxation of long-wavelength density perturbations in a one-dimensional conserved Manna sandpile. Far from criticality where correlation length ξ is finite, relaxation of density profiles having wave numbers k→0 is diffusive, with relaxation time τ_{R}∼k^{-2}/D with D being the density-dependent bulk-diffusion coefficient. Near criticality with kξ≳1, the bulk diffusivity diverges and the transport becomes anomalous; accordingly, the relaxation time varies as τ_{R}∼k^{-z}, with the dynamical exponent z=2-(1-β)/ν_{⊥}<2, where β is the critical order-parameter exponent and ν_{⊥} is the critical correlation-length exponent.

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We derive hydrodynamics of a prototypical one-dimensional model, having variable-range hopping, which mimics passive diffusion and ballistic motion of active, or self-propelled, particles. The model has two main ingredients-the hardcore interaction and the competing mechanisms of short- and long-range hopping. We calculate two density-dependent transport coefficients-the bulk-diffusion coefficient and the conductivity, the ratio of which, despite violation of detailed balance, is connected to particle-number fluctuation by an Einstein relation.

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We study coarse-grained density fluctuations in the disordered phase of the paradigmatic Vicsek-like models of self-propelled particles with alignment interactions and random self-propulsion velocities. By numerically integrating a fluctuation-response relation-the direct consequence of an additivity property-we compute logarithm of the large-deviation probabilities of the coarse-grained subsystem density, while the system is in the disordered fluid phase with vanishing macroscopic velocity. The large-deviation probabilities, computed within additivity, agree remarkably well with that obtained from direct microscopic simulations of the models.

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We study conserved stochastic sandpiles (CSSs), which exhibit an active-absorbing phase transition upon tuning density ρ. We demonstrate that a broad class of CSSs possesses a remarkable hydrodynamic structure: There is an Einstein relation σ^{2}(ρ)=χ(ρ)/D(ρ), which connects bulk-diffusion coefficient D(ρ), conductivity χ(ρ), and mass fluctuation, or scaled variance of subsystem mass, σ^{2}(ρ). Consequently, density large-deviations are governed by an equilibrium-like chemical potential μ(ρ)∼lna(ρ), where a(ρ) is the activity in the system.

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We derive hydrodynamics of paradigmatic conserved-mass transport processes on a ring. The systems, governed by chipping, diffusion, and coalescence of masses, eventually reach a nonequilibrium steady state, having nontrivial correlations, with steady-state measures in most cases not known. In these processes, we analytically calculate two transport coefficients, bulk-diffusion coefficient and conductivity.

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We exactly calculate two-point spatial correlation functions in steady state in a broad class of conserved-mass transport processes, which are governed by chipping, diffusion, and coalescence of masses. We find that the spatial correlations are in general short-ranged and, consequently, on a large scale, these transport processes possess a remarkable thermodynamic structure in the steady state. That is, the processes have an equilibrium-like additivity property and, consequently, a fluctuation-response relation, which help us to obtain subsystem mass distributions in the limit of subsystem size large.

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We study symmetric simple exclusion processes (SSEP) on a ring in the presence of uniformly moving multiple defects or disorders-a generalization of the model we proposed earlier [Phys. Rev. E 89, 022138 (2014)PLEEE81539-375510.

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Using an additivity property, we study particle-number fluctuations in a system of interacting self-propelled particles, called active Brownian particles (ABPs), which consists of repulsive disks with random self-propulsion velocities. From a fluctuation-response relation, a direct consequence of additivity, we formulate a thermodynamic theory which captures the previously observed features of nonequilibrium phase transition in the ABPs from a homogeneous fluid phase to an inhomogeneous phase of coexisting gas and liquid. We substantiate the predictions of additivity by analytically calculating the subsystem particle-number distributions in the homogeneous fluid phase away from criticality where analytically obtained distributions are compatible with simulations in the ABPs.

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We show that an equilibriumlike additivity property can remarkably lead to power-law distributions observed frequently in a wide class of out-of-equilibrium systems. The additivity property can determine the full scaling form of the distribution functions and the associated exponents. The asymptotic behavior of these distributions is solely governed by branch-cut singularity in the variance of subsystem mass.

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We study a class of nonequilibrium lattice models on a ring where particles hop in a particular direction, from a site to one of its (say, right) nearest neighbors, with a rate that depends on the occupation of all the neighboring sites within a range R. This finite-range process (FRP) for R=0 reduces to the well-known zero-range process (ZRP), giving rise to a factorized steady state (FSS) for any arbitrary hop rate. We show that, provided the hop rates satisfy a specific condition, the steady state of FRP can be written as a product of a cluster-weight function of (R+1) occupation variables.

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We ask what happens when two nonequilibrium systems in steady state are kept in contact and allowed to exchange a quantity, say mass, which is conserved in the combined system. Will the systems eventually evolve to a new stationary state where a certain intensive thermodynamic variable, like equilibrium chemical potential, equalizes following the zeroth law of thermodynamics and, if so, under what conditions is it possible? We argue that an equilibriumlike thermodynamic structure can be extended to nonequilibrium steady states having short-ranged spatial correlations, provided that the systems interact weakly to exchange mass with rates satisfying a balance condition-reminiscent of a detailed balance condition in equilibrium. The short-ranged correlations would lead to subsystem factorization on a coarse-grained level and the balance condition ensures both equalization of an intensive thermodynamic variable as well as ensemble equivalence, which are crucial for construction of a well-defined nonequilibrium thermodynamics.

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We study a system of interacting particles in a periodically moving external potential, within the simplest possible description of paradigmatic symmetric exclusion process on a ring. The model describes diffusion of hardcore particles where the diffusion dynamics is locally modified at a uniformly moving defect site, mimicking the effect of the periodically moving external potential. The model, though simple, exhibits remarkably rich features in particle transport, such as polarity reversal and double peaks in particle current upon variation of defect velocity and particle density.

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We show that, in conserved-mass transport processes, the steady-state distribution of mass in a subsystem is uniquely determined from the functional dependence of variance of the subsystem mass on its mean, provided that the joint mass distribution of subsystems is factorized in the thermodynamic limit. The factorization condition is not too restrictive as it would hold in systems with short-ranged spatial correlations. To demonstrate the result, we revisit a broad class of mass transport models and its generic variants, and show that the variance of the subsystem mass in these models is proportional to the square of its mean.

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We formulate an approximate thermodynamic theory of the phase transition in driven lattice gases with attractive nearest-neighbor interactions. We construct the van der Waals equation of state for a driven system where a nonequilibrium chemical potential can be expressed as a function of density and driving field. A Maxwell's construction leads to the phase transition from a homogeneous fluid phase to the coexisting phases of gas and liquid.

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For a class of nonequilibrium systems, called driven lattice gases, we study what happens when two systems are kept in contact and allowed to exchange particles with the total number of particles conserved. For both attractive and repulsive nearest-neighbor interactions among particles and for a wide range of parameter values, we find that, to a good approximation, one could define an intensive thermodynamic variable, such as the equilibrium chemical potential, that determines the final steady state for two initially separated driven lattice gases brought into contact. However, due to nontrivial contact dynamics, there are also observable deviations from this simple thermodynamic law.

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We explore driven lattice gases for the existence of an intensive thermodynamic variable which could determine "equilibration" between two nonequilibrium steady-state systems kept in weak contact. In simulations, we find that these systems satisfy surprisingly simple thermodynamic laws, such as the zeroth law and the fluctuation-response relation between the particle-number fluctuation and the corresponding susceptibility remarkably well. However, at higher densities, small but observable deviations from these laws occur due to nontrivial contact dynamics and the presence of long-range spatial correlations.

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We study charge transport in an ionic solution in a confined nanoscale geometry in the presence of an externally applied electric field and immobile background charges. For a range of parameters, the ion current shows nonmonotonic behavior as a function of the external ion concentration. For small applied electric field, the ion transport can be understood from simple analytic arguments, which are supported by Monte Carlo simulations.

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We study nonequilibrium fluctuation theorems for classical systems in the presence of a time-reversal symmetry-breaking field and nonconservative forces in a stochastic as well as a deterministic setup. We consider a system and a heat bath, called the combined system, and show that the fluctuation theorems are valid even when the heat bath goes out of equilibrium during driving. The only requirement for the validity is that, when the driving is switched off, the combined system relaxes to a state having a uniform probability measure on a constant energy surface, consistent with microcanonical ensemble of an isolated system.

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