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Solutions to Master Equations of Quantum Brownian Motion in a General Environment with External Force

Albert Roura, Christen H. Fleming, B. L. Hu

Published May 18, 2007• 0 citations
OpenAlex

Abstract

We revisit the model of a system made up of a Brownian quantum oscillator linearly coupled to an environment made up of many quantum oscillators at finite temperature. We show that the HPZ master equation for the reduced density matrix derived earlier [B.L. Hu, J.P. Paz, Y. Zhang, Phys. Rev. D 45, 2843 (1992)] has incorrectly specified coefficients for the case of nonlocal dissipation. We rederive the QBM master equation, correctly specifying all coefficients, and determine the position uncertainty to be free of excessive cutoff sensitivity. Our coefficients and solutions are reduced entirely to contour integration for analytic spectra at arbitrary temperature, coupling strength, and cut-off. As an illustration we calculate the master equation coefficients and solve the master equation for ohmic coupling (with finite cutoff) and example supra-ohmic and sub-ohmic spectral densities. We determine the effect of an external force on the quantum oscillator and also show that our representation of the master equation and solutions naturally extends to a system of multiple oscillators bilinearly coupled to themselves and the bath in arbitrary fashion. This produces a formula for investigating the standard quantum limit which is central to addressing many theoretical issues in macroscopic quantum phenomena and experimental concerns related to low temperature precision measurements. We find that in a dissipative environment, all initial states settle down to a Gaussian density matrix whose covariance is determined by the thermal reservoir and whose mean is determined by the external force. We specify the thermal covariance for the spectral densities we explore.

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Solutions to Master Equations of Quantum Brownian Motion in a General Environment with External Force

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We revisit the model of a system made up of a Brownian quantum oscillator under the influence of an external classical force and linearly coupled to an environment made up of many quantum oscillators at zero or finite temperature. We show that the HPZ master equation for the reduced density matrix derived earlier [B.L. Hu, J.P. Paz, Y. Zhang, Phys. Rev. D 45, 2843 (1992)] with coefficients obtained from solutions of integro-differential equations can assume closed functional forms for a fairly general class of spectral densities of the environment at arbitrary temperature and coupling strength. As an illustration of these new results we solve the corresponding master equation and calculate, among other physical quantities, the uncertainty function whose late time behavior can be obtained fully. This produces a formula for investigating the standard quantum limit which is central to addressing many theoretical issues in macroscopic quantum phenomena and experimental concerns related to low temperature precision measurements. We find that any initial state always settles down to a Gaussian density matrix whose covariance is determined by the thermal reservoir and whose mean is determined by the external force. For more general spectra we show that the solution of the master equation can be reduced to solving for the motion of a classical parametric oscillator with parametric frequency determined by the unsolved for master equation coefficients. States in these systems experience evolution that is parametrically similar to the simpler evolution explicitly determined for in the case of Laurent-series spectra.

arXiv:0705.2766•May 18, 2007•3 citations

Exact analytical solutions to the master equation of quantum Brownian motion for a general environment

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We revisit the model of a quantum Brownian oscillator linearly coupled to an environment of quantum oscillators at finite temperature. By introducing a compact and particularly well-suited formulation, we give a rather quick and direct derivation of the master equation and its solutions for general spectral functions and arbitrary temperatures. The flexibility of our approach allows for an immediate generalization to cases with an external force and with an arbitrary number of Brownian oscillators. More importantly, we point out an important mathematical subtlety concerning boundary-value problems for integro-differential equations which led to incorrect master equation coefficients and impacts on the description of nonlocal dissipation effects in all earlier derivations. Furthermore, we provide explicit, exact analytical results for the master equation coefficients and its solutions in a wide variety of cases, including ohmic, sub-ohmic and supra-ohmic environments with a finite cut-off.

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Momentum coupling in non-Markovian quantum Brownian motion

Luca Ferialdi, Andrea Smirne

We consider a model of non-Markovian quantum Brownian motion that consists of a harmonic oscillator bilinearly coupled to a thermal bath, both via its position and via its momentum operators. We derive the master equation for such a model, and we solve the equations of motion for a generic Gaussian system state. We then investigate the resulting evolution of the first and second moments for both an Ohmic and a super-Ohmic spectral density. In particular, we show that, irrespective of the specific form of the spectral density, the coupling with the momentum enhances the dissipation experienced by the system, accelerating its relaxation to the equilibrium as well as modifying the asymptotic state of the dynamics. Eventually, we characterize explicitly the non-Markovianity of the evolution using a general criterion which relies on the positivity of the master equation coefficients.

arXiv:1705.06245•Physical Review A•Jul 11, 2017•26 citations
We revisit the model of a system made up of a Brownian quantum oscillator linearly coupled to an environment made up of many quantum oscillators at finite temperature. We show that the HPZ master equation for the reduced density matrix derived earlier [B.L. Hu, J.P. Paz, Y. Zhang, Phys. Rev. D 45, 2843 (1992)] has incorrectly specified coefficients for the case of nonlocal dissipation. We rederive the QBM master equation, correctly specifying all coefficients, and determine the position uncertainty to be free of excessive cutoff sensitivity. Our coefficients and solutions are reduced entirely to contour integration for analytic spectra at arbitrary temperature, coupling strength, and cut-off. As an illustration we calculate the master equation coefficients and solve the master equation for ohmic coupling (with finite cutoff) and example supra-ohmic and sub-ohmic spectral densities. We determine the effect of an external force on the quantum oscillator and also show that our representation of the master equation and solutions naturally extends to a system of multiple oscillators bilinearly coupled to themselves and the bath in arbitrary fashion. This produces a formula for investigating the standard quantum limit which is central to addressing many theoretical issues in macroscopic quantum phenomena and experimental concerns related to low temperature precision measurements. We find that in a dissipative environment, all initial states settle down to a Gaussian density matrix whose covariance is determined by the thermal reservoir and whose mean is determined by the external force. We specify the thermal covariance for the spectral densities we explore.
We revisit the model of a system made up of a Brownian quantum oscillator under the influence of an external classical force and linearly coupled to an environment made up of many quantum oscillators at zero or finite temperature. We show that the HPZ master equation for the reduced density matrix derived earlier [B.L. Hu, J.P. Paz, Y. Zhang, Phys. Rev. D 45, 2843 (1992)] with coefficients obtained from solutions of integro-differential equations can assume closed functional forms for a fairly general class of spectral densities of the environment at arbitrary temperature and coupling strength. As an illustration of these new results we solve the corresponding master equation and calculate, among other physical quantities, the uncertainty function whose late time behavior can be obtained fully. This produces a formula for investigating the standard quantum limit which is central to addressing many theoretical issues in macroscopic quantum phenomena and experimental concerns related to low temperature precision measurements. We find that any initial state always settles down to a Gaussian density matrix whose covariance is determined by the thermal reservoir and whose mean is determined by the external force. For more general spectra we show that the solution of the master equation can be reduced to solving for the motion of a classical parametric oscillator with parametric frequency determined by the unsolved for master equation coefficients. States in these systems experience evolution that is parametrically similar to the simpler evolution explicitly determined for in the case of Laurent-series spectra.
We revisit the model of a quantum Brownian oscillator linearly coupled to an environment of quantum oscillators at finite temperature. By introducing a compact and particularly well-suited formulation, we give a rather quick and direct derivation of the master equation and its solutions for general spectral functions and arbitrary temperatures. The flexibility of our approach allows for an immediate generalization to cases with an external force and with an arbitrary number of Brownian oscillators. More importantly, we point out an important mathematical subtlety concerning boundary-value problems for integro-differential equations which led to incorrect master equation coefficients and impacts on the description of nonlocal dissipation effects in all earlier derivations. Furthermore, we provide explicit, exact analytical results for the master equation coefficients and its solutions in a wide variety of cases, including ohmic, sub-ohmic and supra-ohmic environments with a finite cut-off.
In this paper we derive an exact master equation for two coupled quantum harmonic oscillators interacting via bilinear coupling with a common environment at arbitrary temperature made up of many harmonic oscillators with a general spectral density function. We first show a simple derivation based on the observation that the two harmonic oscillator model can be effectively mapped into that of a single harmonic oscillator in a general environment plus a free harmonic oscillator. Since the exact one harmonic oscillator master equation is available [B. L. Hu, J. P. Paz, and Y. Zhang, Phys. Rev. D 45, 2843 (1992)], the exact master equation with all its coefficients for this two harmonic oscillator model can be easily deduced from the known results of the single harmonic oscillator case. In the second part we give an influence functional treatment of this model and provide explicit expressions for the evolutionary operator of the reduced density matrix which are useful for the study of decoherence and disentanglement issues. We show three applications of this master equation: on the decoherence and disentanglement of two harmonic oscillators due to their interaction with a common environment under Markovian approximation, and a derivation of the uncertainty principle at finite temperature for a composite object, modeled by two interacting harmonic oscillators. The exact master equation for two, and its generalization to N, harmonic oscillators interacting with a general environment are expected to be useful for the analysis of quantum coherence, entanglement, fluctuations, and dissipation of mesoscopic objects toward the construction of a theoretical framework for macroscopic quantum phenomena.
Abstract After replacing the reduced density matrix of a quantum harmonic oscillator linearly coupled to a thermal bath by its ‘characteristic function’ (a non-negative definite function defined on the Heisenberg-Weyl group), the master equation of the reduced density matrix can be transformed into a first-order linear partial differential equation of the characteristic function. We derive stationary solutions for the Caldeira–Leggett (CL) master equation as well as for the late-time Hu–Paz–Zhang master equation, and examine the positivity problem for these solutions. In order to illustrate to what extent classical properties of quantum states of the damping oscillator emerge dynamically due to coupling to the environment, we discuss the problem of how and under what conditions a steady state predicted by the CL master equation could be expressed as a statistical mixture of Gaussian packets having a uniform position variance. Similar studies are carried out for the solutions of a Lindblad-form generalization of the CL master equation, where the positivity problem is certainly absent. Our results show that in the low-temperature regime the steady states predicted by the Lindblad-type master equation may depend on the damping strength of the bath and there are cases which may not show Gaussian-packet decomposition.
For the purpose of understanding the quantum behavior such as quantum decoherence, fluctuations, dissipation, entanglement and teleportation of a mesoscopic or macroscopic object interacting with a general environment, we derive here a set of exact master equations for the reduced density matrix of N interacting harmonic oscillators in a heat bath with arbitrary spectral density and temperature. For the case N = 2, we also give an influence functional treatment of this model and provide explicit expressions for the evolution operator of the reduced density matrix which are useful for the study of decoherence and disentanglement issues. We show a simple application of this master equation by examining the decoherence and disentanglement of two harmonic oscillators due to their interaction with a common environment under Markovian approximation. Two classes of problems of interest to us which these equations can be usefully applied to are that of the quantum dynamics of nanoelectromechanical oscillators and the entanglement evolution of multi-partite macroscopic states such as quantum superposition of mirrors in a high Q cavity. To address a key conceptual issue for macroscopic quantum phenomena we examine the conditions for an assumption often implicitly made in these studies to be valid, namely, that the quantum behavior of a macroscopic object in an environment can be accurately represented by only treating the dynamics of its center-of-mass variable. We also mention how these results can be used to calculate the uncertainty principle governing a macroscopic object at finite temperature.
We consider a model of non-Markovian quantum Brownian motion that consists of a harmonic oscillator bilinearly coupled to a thermal bath, both via its position and via its momentum operators. We derive the master equation for such a model, and we solve the equations of motion for a generic Gaussian system state. We then investigate the resulting evolution of the first and second moments for both an Ohmic and a super-Ohmic spectral density. In particular, we show that, irrespective of the specific form of the spectral density, the coupling with the momentum enhances the dissipation experienced by the system, accelerating its relaxation to the equilibrium as well as modifying the asymptotic state of the dynamics. Eventually, we characterize explicitly the non-Markovianity of the evolution using a general criterion which relies on the positivity of the master equation coefficients.