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arXiv:cond-mat/0611681 · Physical Review E

Intensive thermodynamic parameters in nonequilibrium systems

Éric Bertin, Kirsten Martens, Olivier Dauchot, Michel Droz

Published Mar 29, 2007• 49 citations
arXivHTMLPDF

Abstract

Considering a broad class of steady-state nonequilibrium systems for which some additive quantities are conserved by the dynamics, we introduce from a statistical approach intensive thermodynamic parameters (ITPs) conjugated to the conserved quantities. This definition does not require any detailed balance relation to be fulfilled. Rather, the system must satisfy a general additivity property, which holds in most of the models usually considered in the literature, including those described by a matrix product ansatz with finite matrices. The main property of these ITPs is to take equal values in two subsystems, making them a powerful tool to describe nonequilibrium phase coexistence, as illustrated on different models. We finally discuss the issue of the equalization of ITPs when two different systems are put into contact. This issue is closely related to the possibility of measuring the ITPs using a small auxiliary system, in the same way as temperature is measured with a thermometer, and points at one of the major difficulties of nonequilibrium statistical mechanics. In addition, an efficient alternative determination, based on the measure of fluctuations, is also proposed and illustrated.

DOI
10.1103/physreve.75.031120

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Considering a broad class of steady-state nonequilibrium systems for which some additive quantities are conserved by the dynamics, we introduce from a statistical approach intensive thermodynamic parameters (ITPs) conjugated to the conserved quantities. This definition does not require any detailed balance relation to be fulfilled. Rather, the system must satisfy a general additivity property, which holds in most of the models usually considered in the literature, including those described by a matrix product ansatz with finite matrices. The main property of these ITPs is to take equal values in two subsystems, making them a powerful tool to describe nonequilibrium phase coexistence, as illustrated on different models. We finally discuss the issue of the equalization of ITPs when two different systems are put into contact. This issue is closely related to the possibility of measuring the ITPs using a small auxiliary system, in the same way as temperature is measured with a thermometer, and points at one of the major difficulties of nonequilibrium statistical mechanics. In addition, an efficient alternative determination, based on the measure of fluctuations, is also proposed and illustrated.
We consider the general problem of determining the steady state of stochastic nonequilibrium systems such as those that have been used to model (among other things) biological transport and traffic flow. We begin with a broad overview of this class of driven diffusive systems - which includes exclusion processes - focusing on interesting physical properties, such as shocks and phase transitions. We then turn our attention specifically to those models for which the exact distribution of microstates in the steady state can be expressed in a matrix product form. In addition to a gentle introduction to this matrix product approach, how it works and how it relates to similar constructions that arise in other physical contexts, we present a unified, pedagogical account of the various means by which the statistical mechanical calculations of macroscopic physical quantities are actually performed. We also review a number of more advanced topics, including nonequilibrium free energy functionals, the classification of exclusion processes involving multiple particle species, existence proofs of a matrix product state for a given model and more complicated variants of the matrix product state that allow various types of parallel dynamics to be handled. We conclude with a brief discussion of open problems for future research.
Abstract A phase coexistence state cannot be specified uniquely by any intensive parameters, such as the temperature and the magnetic field, because they take the same values over all coexisting phases. It can be specified uniquely only by an appropriate set of additive observables. Hence, to analyze phase coexistence states the statistical ensembles that are specified by additive observables have been employed, such as the microcanonical and restricted ensembles. However, such ensembles are ill-defined or ill-behaved when some of the additive observables do not commute with each other. Here, we solve this fundamental problem by extending a generalized ensemble in such a way that it is applicable to phase coexistence states that are specified by noncommutative additive observables. We prove that this ensemble correctly gives the density matrix corresponding to phase coexistence states of general quantum systems as well as the thermodynamic functions. Furthermore, these ensembles are convenient for practical calculations because of their good analytic properties and useful formulas by which temperature and other intensive parameters are directly obtained from the expectation values of the additive observables. As a demonstration, we apply our formulation to a two-dimensional system whose phase coexistence states are specified by an additive observable (order parameter) that does not commute with the Hamiltonian.
We consider the generic model of a finite-size quantum electron system connected to two (temperature and particle) reservoirs. The quantum open system is driven out of equilibrium by the presence of both potential temperature and chemical differences between the two reservoirs. The nonequilibrium (NE) thermodynamical properties of such a quantum open system are studied for the steady state regime. In such a regime, the corresponding NE density matrix is built on the so-called generalised Gibbs ensembles. From different expressions of the NE density matrix, we can identify the terms related to the entropy production in the system. We show, for a simple model, that the entropy production rate is always a positive quantity. Alternative expressions for the entropy production are also obtained from the Gibbs–von Neumann conventional formula and discussed in detail. Our results corroborate and expand earlier works found in the literature.
Coexisting phases in a phase coexistence state cannot be distinguished by thermodynamic forces, such as temperature and chemical potential, because the forces take the same values over all coexisting phases. Therefore, to investigate a phase coexistence state, it is necessary to employ an ensemble in which all additive observables that distinguish the coexisting phases have macroscopically definite values. Although the microcanonical ensemble is conventionally employed as such an ensemble, it becomes ill-defined when some of the additive observables do not commute with each other, and a new ensemble has been craved. We propose a novel class of ensembles such that the additive observables, which are generally noncommutative, always have macroscopically definite values even in a first-order phase transition region. Using these ensembles, we propose a concrete method to construct phase coexistence states of general quantum systems. Furthermore, these ensembles are convenient for practical calculations because of good analytic properties. To demonstrate that our formulation successfully gives phase coexistence states of quantum systems, we apply it to a two-dimensional system whose coexisting phases are distinguished by an additive observable (order parameter) that does not commute with the Hamiltonian. To the author's best knowledge, this is the first work that obtains phase coexistence states separated by phase interfaces at finite temperature in such a quantum system.
We explore some aspects of nonequilibrium statistical mechanics of classical and quantum systems. Two chapters are devoted to fluctuation theorems which were originally derived for classical systems. The main challenge in formulating them in quantum mechanics is the fact that fundamental quantities of interest, like work, are defined via the classical concept of a phase space trajectory. We utilize the decoherent histories conceptual framework, in which classical trajectories emerge in quantum mechanics as a result of coarse graining, and provide a first-principles analysis of the nonequilibrium work relation of Jarzynski and Crooks's fluctuation theorem for a quantum system interacting with a general environment based on the quantum Brownian motion (QBM) model. We indicate a parameter range at low temperatures where the theorems might fail in their original form. Fluctuation theorems of Jarzynski and Crooks for systems obeying classical Hamiltonian dynamics are derived under the assumption that the initial conditions are sampled from a canonical ensemble, even though the equilibrium state of an isolated system is typically associated with the microcanonical ensemble. We address this issue through an exact analysis of the classical Brownian motion model. We argue that a stronger form of ensemble equivalence than usually discussed in equilibrium statistical mechanics is required for these theorems to hold in the infinite environment limit irrespective of the ensemble used, and proceed to prove it for this model. An exact expression for the probability distribution of work is obtained for finite environments. Intuitively one expects a system to relax to an equilibrium state when brought into contact with a thermal environment. Yet it is important to have rigorous results that provide conditions for equilibration and characterize the equilibrium state. We consider the dynamics of open quantum systems using the Langevin and master equations and rigorously show that under fairly general conditions quantum systems interacting with a heat bath relax to the equilibrium state defined as the reduced thermal state of the system plus environment, even in the strong coupling regime. Our proof is valid to second-order in interaction strength for general systems and exact for the linear QBM model, for which we also show the equivalence of multi-time correlations. In the final chapter we give a sampling of our investigations into macroscopic quantum phenomena. We work out in detail a specific example of how and under what conditions the center of mass (CoM) coordinate of a macroscopic object emerges as the relevant degree of freedom. Interaction patterns are studied in terms of the couplings they induce between the CoM and relative coordinates of two macroscopic objects. We discuss the implications of these interaction patterns on macroscopic entanglement.
A theory of non-equilibrium thermodynamics is developed. The general method to derive the closed set of kinetic equations for expectation values of physical quantities is developed, by making use of the functional Taylor expansion with respect to expectation values of physical quantities around the reference state. For this purpose, a definition of the thermodynamic state in the system whose state changes with time is presented in order to describe the general state of the many-body system from the unified point of view. The statistical mechanical probability distribution functions for the quantum-mechanical expectation values at the stationary state are developed, without making use of the concept of the constant of the motion. The relation between the expectation value and the most probable value for the probability distribution function is discussed, and it is found that both values are equivalent to each other, if the system is extended infinitely in space and time. Thus the condition for the thermodynamic limit may be defined in a generalized way. Our method is looked as a perturbational one in the equilibrium statistical mechanics, though the choice of the reference state is arbitrary.