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arXiv:1902.07645

Entropies for Coupled Harmonic Oscillators and Temperature

Ahmed Jellal, Abdeldjalil Merdaci

Published Feb 19, 2019• 2 citations
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Abstract

We study two entropies of a system composed of two coupled harmonic oscillators which is brought to a canonical thermal equilibrium with a heat-bath at temperature $T$. Using the purity function, we explicitly determine the Rényi and van Newmon entropies in terms of different physical parameters. We will numerically analyze these two entropies under suitable conditions and show their relevance.

DOI
10.48550/arxiv.1902.07645

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We study two entropies of a system composed of two coupled harmonic oscillators which is brought to a canonical thermal equilibrium with a heat-bath at temperature TTT. Using the purity function, we explicitly determine the Rényi and van Newmon entropies in terms of different physical parameters. We will numerically analyze these two entropies under suitable conditions and show their relevance.
Abstract We consider the thermal aspect of a system composed of two coupled harmonic oscillators and study the corresponding purity. We initially consider a situation where the system is brought to a canonical thermal equilibrium with a heat-bath at temperature T . We adopt the path integral approach and introduce the evolution operator to calculate the density matrix and subsequently the reduced matrix density. It is used to explicitly determine the purity in terms of different physical quantities and therefore study some limiting cases related to temperature as well as other parameters. Different numerical results are reported and discussed in terms of the involved parameters of our system.
Abstract We present an exact analytical solution of the Hu–Paz–Zhang master equation in a precise Markovian limit for a system of two harmonically coupled harmonic oscillators interacting with a common thermal bath of harmonic oscillators. The thermal bath is initially considered to be at arbitrary temperatures and characterized by an Ohmic Lorentz–Drude spectral density. In the examined system, couplings between the two harmonic oscillators and the environment ensure a complete decoupling of the center-of-mass and relative degrees of freedom, resulting in undamped dynamics in the relative coordinate. The exact time evolution is used to analyze the system’s entanglement dynamics, quantified through logarithmic negativity and quantum mutual information, while ensuring the positivity of the density operator to confirm the physical validity of the results. We demonstrate that, under certain parameter regimes and initial conditions, the asymptotic dynamics can give rise to periodic entanglement-disentanglement behavior. Furthermore, numerical simulations reveal that for negative values of the direct coupling between the oscillators, which are sufficiently close to a critical lower bound beyond which the system becomes unstable, the system can maintain entanglement across a broad temperature range and for arbitrarily long durations.
Mode entanglement in a two-mode squeezed state is studied. The entanglement spectrum is derived and interpreted as Boltzmann coefficients of harmonic oscillator eigenstates at thermal equilibrium. The effective temperature is expressed in terms of squeezing parameters and is equal to zero when the state is unsqueezed and increases without bound as the state is infinitely squeezed. It is demonstrated that the reduced density operator can be identified as a canonical ensemble of single harmonic oscillator at some effective temperature Te. The Renyi entanglement entropy is calculated and found to increase without bound as the squeezing parameter increases. The single-copy entanglement, which is a limiting value of the Renyi entropy, is interpreted as a partition function.
The positivity conditions of the relative entropy between two thermal equilibrium states ρ[over ̂]_{1} and ρ[over ̂]_{2} are used to obtain upper and lower bounds for the subtraction of their entropies, the Helmholtz potential and the Gibbs potential of the two systems. These limits are expressed in terms of the mean values of the Hamiltonians, number operator, and temperature of the different systems. In particular, we discuss these limits for molecules that can be represented in terms of the Franck-Condon coefficients. We emphasize the case where the Hamiltonians belong to the same system at two different times t and t^{'}. Finally, these bounds are obtained for a general qubit system and for the harmonic oscillator with a time-dependent frequency at two different times.
We investigate the quantum entanglement of systems of coupled harmonic oscillators on the basis of thermo-field dynamics (TFD). For coupled harmonic oscillators at equilibrium, the extended entanglement entropy is derived using the TFD method, and it is demonstrated to be controlled by temperature and coupling parameters. For non-equilibrium systems, in addition to temperature and coupling parameters, the time dependence of the extended entanglement entropy is calculated in accordance with the dissipative von Neumann equation, and the dissipative dynamics of the systems of coupled harmonic oscillators is discussed. Consequently, based on TFD, the physical parametrization of the entanglement entropies is confirmed in both the equilibrium and non-equilibrium cases of harmonic oscillator systems by means of the laws of thermodynamics.
We study the quantum entanglement of systems of coupled harmonic oscillators on the basis of thermo-field dynamics (TFD).For coupled harmonic oscillators at equilibrium, the extended entanglement entropy is derived using the TFD method, and it is demonstrated to be controlled by temperature and coupling parameters.For non-equilibrium systems, in addition to temperature and coupling parameters, the time dependence of the extended entanglement entropy is calculated in accordance with the dissipative von Neumann equation, and the dissipative dynamics of the systems of coupled harmonic oscillators is discussed.Consequently, based on TFD, the physical parametrization of the entanglement entropies is confirmed in both the equilibrium and nonequilibrium cases of harmonic oscillator systems by means of the laws of thermodynamics.