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Physical Review E

Transport coefficients of a quantum system interacting with a squeezed heat bath

Sh. A. Kalandarov, Z. Kanokov, G. G. Adamian, N. V. Antonenko

Published Jul 26, 2006• 11 citations
Publisher

Abstract

The analytical expressions for the time-dependent friction and diffusion coefficients are presented for the case of coupling in coordinates between the collective subsystem and a squeezed heat bath. The effects of initial phase-sensitive and -insensitive correlations of the heat bath on the diffusion coefficients, fluctuations, and decoherence are studied. The interplay between friction and decoherence is discussed.

DOI
10.1103/physreve.74.011118

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The analytical expressions for the time-dependent friction and diffusion coefficients are presented for the case of coupling in coordinates between the collective subsystem and a squeezed heat bath. The effects of initial phase-sensitive and -insensitive correlations of the heat bath on the diffusion coefficients, fluctuations, and decoherence are studied. The interplay between friction and decoherence is discussed.
Quantum diffusion equations featuring explicitly time-dependent transport coefficients are derived from generalized non-Markovian Langevin equations. Generalized fluctuation-dissipation relations and analytic expressions for calculating the friction and diffusion coefficients in nuclear processes are obtained. The asymptotic behavior of the transport coefficients and correlation functions for a damped harmonic oscillator that is linearly coupled in momentum to a heat bath is studied. The coupling to a heat bath in momentum is responsible for the appearance of the diffusion coefficient in coordinate. The problem of regression of correlations in quantum dissipative systems is analyzed.
The system of nonlinear Langevin equations was obtained by using Hamiltonian's operator of two coupling quantum oscillators which are interacting with heat bath. By using the analytical solution of these equations, the analytical expressions for transport coefficients was found. Generalized Langevin equations and fluctuation-dissipation relations are derived for the case of a nonlinear non-Markovian noise. The explicit expressions for the time-dependent friction and diffusion coefficients are presented for the case of linear couplings in the coordinate between the collective two coupled harmonic oscillators and heat bath.
We study the dynamics of the quantum phase distribution associated with the reduced density matrix of a system for a number of situations of practical importance, as the system evolves under the influence of its environment, interacting via a quantum nondemolition type of coupling, such that there is decoherence without dissipation, as well as when it interacts via a dissipative interaction, resulting in decoherence as well as dissipation. The system is taken to be either a two-level atom (or, equivalently, a spin-1∕21∕21∕2 system) or a harmonic oscillator, and the environment is modeled as a bath of harmonic oscillators, starting out in a squeezed thermal state. The impact of the different environmental parameters on the dynamics of the quantum phase distribution for the system starting out in various initial states is explicitly brought out. An interesting feature that emerges from our work is that the relationship between squeezing and temperature effects depends on the type of system-bath interaction. In the case of a quantum nondemolition type of interaction, squeezing and temperature work in tandem, producing a diffusive effect on the phase distribution. In contrast, in the case of a dissipative interaction, the influence of temperature can be counteracted by squeezing, which manifests as a resistance to randomization of phase. We make use of the phase distributions to bring out a notion of complementarity in atomic systems. We also study the variance of the phase using phase distributions conditioned on particular initial states of the system.
Abstract We study a cascaded system of two subsystems repeatedly interacting with a bath prepared in various non-thermal states. Effects of different types of bath coherence on dynamics of the system heat flux are explored. For a single-qubit bath with the displacement coherence, heat flux of each subsystem is divided into dissipative and coherent parts. In the stationary regime, the dissipative heat fluxes are the same for the two subsystems, but the coherent parts are not due to the cascaded feature. In the transient regime, heat fluxes occur even when the system and the bath have the same temperature and, more surprisingly, heat flow reversal appears when temperatures of the system and the bath differ. For a two-qubit bath we consider two types of coherence: the squeezing and the heat-exchange ones. In the stationary regime, the squeezing coherence establishes correlations between the subsystems, each of which is evolving to its thermal state with a temperature identical to the bath’s. The squeezing coherence slightly influences only the dynamics of the subsystem that interacts with the bath later. As for the heat-exchange coherence, it forces the total system to thermalize to a state with the temperature related to both magnitude and relative phase of the coherence. Particularly, depending on the relative phases, the heat-exchange coherence can amplify or suppress the heat flux during the time evolution.
The dynamics of a mixed quantum-classical system, in which the classical subsystem interacts with a dissipative bath, is investigated. This description of the dynamics will be appropriate if the details of the bath dynamics are unimportant but its presence plays an important role in the dissipation of energy to the environment. In this dynamical description, which can be simulated employing an ensemble of stochastic surface-hopping trajectories, the strength of the dissipation is controlled by a friction coefficient. We show that if decoherence, whose effects are controlled by the bath friction, is sufficiently rapid, the equation of motion can be reduced to a master equation. Thus, decoherence and the validity of master equation models may be explored as a function of bath friction. We use this framework to study the mechanism of decoherence in a simple model nonadiabatic chemical reaction.