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arXiv:1207.3700 · New Journal of Physics

Role of correlations in the thermalization of quantum systems

Andrea Smirne, E-M Laine, Heinz‐Peter Breuer, Jyrki Piilo, Bassano Vacchini

Published Nov 22, 2012• 4 citations
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Abstract

We investigate the equilibration and thermalization properties of quantum systems interacting with a finite dimensional environment. By exploiting the concept of time averaged states, we introduce a completely positive map which allows to describe in a quantitative way the dependence of the equilibrium state on the initial condition. Our results show that the thermalization of quantum systems is favored if the dynamics induces small system-environment correlations, as well as small changes in the environment, as measured by the trace distance.

DOI
10.1088/1367-2630/14/11/113034

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We investigate the equilibration and thermalization properties of quantum systems interacting with a finite dimensional environment. By exploiting the concept of time averaged states, we introduce a completely positive map which allows to describe in a quantitative way the dependence of the equilibrium state on the initial condition. Our results show that the thermalization of quantum systems is favored if the dynamics induces small system-environment correlations, as well as small changes in the environment, as measured by the trace distance.
Two identical finite quantum systems prepared initially at different temperatures, isolated from the environment, and subsequently brought into contact are demonstrated to relax towards Gibbs-like quasi-equilibrium states with a common temperature and small fluctuations around the time-averaged expectation values of generic observables. The temporal thermalization process proceeds via a chain of intermediate Gibbs-like states. We specify the conditions under which this scenario occurs and corroborate the quantum equilibration with two different models.
Employing the trace distance as a measure for the distinguishability of quantum states, we study the influence of initial correlations on the dynamics of open systems. We concentrate on the Jaynes-Cummings model for which the knowledge of the exact joint dynamics of system and reservoir allows the treatment of initial states with arbitrary correlations. As a measure for the correlations in the initial state we consider the trace distance between the system-environment state and the product of its marginal states. In particular, we examine the correlations contained in the thermal equilibrium state for the total system, analyze their dependence on the temperature and on the coupling strength, and demonstrate their connection to the entanglement properties of the eigenstates of the Hamiltonian. A detailed study of the time dependence of the distinguishability of the open system states evolving from the thermal equilibrium state and its corresponding uncorrelated product state shows that the open system dynamically uncovers typical features of the initial correlations.
Two identical finite quantum systems prepared initially at different temperatures, isolated from the environment, and subsequently brought into contact are demonstrated to relax towards Gibbs-like quasiequilibrium states with a common temperature and small fluctuations around the time-averaged expectation values of generic observables. The temporal thermalization process proceeds via a chain of intermediate Gibbs-like states. We specify the conditions under which this scenario occurs and corroborate the quantum equilibration with two different models.
Thermalization in open systems coupled to macroscopic environments is usually analyzed from the perspective of relaxation of the reduced state of the system to the equilibrium state. Less emphasis is given to the change of the state of the bath. However, as previously shown for some specific models, during the thermalization the environment may undergo a nontrivial dynamics, indicated by the the change of its von Neumann entropy, at timescales even longer than the relaxation time of the system; here such a behavior is called post-thermalization. We provide a more detailed analysis of this phenomenon by simulating the full dynamics of a variety of systems together with their environment. In particular, the post-thermalization is qualitatively explained as a result of reconversion of the initially built up correlation between the system and the bath into the correlation between the degrees of freedom in the environment. We also present exemplary systems in which such a reconversion is suppressed due to non-Markovian dynamics or the presence of interactions.
We study the role of correlations with the environment as the source of non-Markovian quantum evolutions. We first focus on the impact that correlations with the environment can have on the dynamical map that evolve the system. We expand the set of initial states of a system and its environment that are known to guarantee completely positive reduced dynamics for the system when the combined state evolves unitarily. We characterize the correlations in the initial state in terms of its quantum discord. The induced maps can be not completely positive when quantum correlations including, but not limited to, entanglement are present. We discuss the implications and limitations of the Markov approximation necessary to derive the Kossakowski-Lindblad master equation. A generalized non-Markovian master equation is derived from the dynamical map of systems correlated with their environment. The physical meaning of not completely positive maps is studied to obtain a consistent theory of non-Markovian quantum dynamics. These are associated to inverse maps necessary to establish correlations and they give rise to a canonical embedding map that is local in time. This master equation goes beyond the Kossakowski-Lindblad master equation. Non-equilibrium quantum thermodynamics can be be studied within this theory. Through out this discussion, the general dynamics of two interacting qubits is used as an example for illustrations.
Simulations are performed of a small quantum system interacting with a quantum environment. The system consists of various initial states of two harmonic oscillators coupled to give normal modes. The environment is "designed" by its level pattern to have a thermodynamic temperature. A random coupling causes the system and environment to become entangled in the course of time evolution. The approach to a Boltzmann distribution is observed, and effective fitted temperatures close to the designed temperature are obtained. All initial pure states of the system are driven to equilibrium at very similar rates, with quick loss of memory of the initial state. The time evolution of the von Neumann entropy is calculated as a measure of equilibration and of quantum coherence. It is pointed out using spatial density distribution plots that quantum interference is eliminated only with maximal entropy, which corresponds thermally to infinite temperature. Implications of our results for the notion of "classicalizing" behavior in the approach to thermal equilibrium are briefly considered.