Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1204.4132 · Physical Review E

Reentrant enhancement of quantum fluctuations for symmetric environmental coupling

Alessandro Cuccoli, Niccolò Del Sette, Ruggero Vaia

Published Apr 15, 2010• 11 citations
arXivHTMLPDF

Abstract

The system-plus-reservoir (SPR) model is the most common and effective approach to study quantum dissipative effects. Indeed, it makes quantization possible by considering the whole energy-conserving system, while the reservoir's degrees of freedom, assumed to be harmonic, can be traced out by the path-integral technique, leading to a formulation that only includes the system of interest. In the standard SPR model the environment is only coupled with the system's coordinate and turns out to quench its quantum fluctuations. However, there are physical systems coupled with an environment whose "coordinates" and "momenta" can be completely interchangeable (e.g., magnets), so an SPR coupling must symmetrically affect both canonical variables. In this paper such a general environmental coupling is studied in the case of a harmonic oscillator. It is found that quantum fluctuations are generally enhanced by environmental coupling with an unexpected nonmonotonic behavior. This leads one to speculate about the possibility that spin-lattice coupling could drive the two-dimensional Heisenberg antiferromagnet to reach its quantum-critical point.

DOI
10.1103/physreve.81.041110

Related papers

Quantum thermodynamics of systems with anomalous dissipative coupling

Alessandro Cuccoli, Andrea Fubini, V. Tognetti +1 more

The standard system-plus-reservoir approach used in the study of dissipative systems can be meaningfully generalized to a dissipative coupling involving the momentum, instead of the coordinate: the corresponding equation of motion differs from the Langevin equation, so this is called anomalous dissipation. It occurs for systems where such coupling can indeed be derived from the physical analysis of the degrees of freedom that can be treated as a dissipation bath. Starting from the influence functional corresponding to anomalous dissipation, it is shown how to derive the effective classical potential that gives the quantum thermal averages for the dissipative system in terms of classical-like calculations; the generalization to many degrees of freedom is given. The formalism is applied to a single particle in a double well and to the discrete phi(4) model. At variance with the standard case, the fluctuations of the coordinate are enhanced by anomalous dissipative coupling.

arXiv:cond-mat/0109018•Physical review. E, Statistical physics, plasmas, fluids, and related interdisciplinary topics•Nov 26, 2001•34 citations

ENVIRONMENTAL EFFECTS ON THE THERMODYNAMICS OF QUANTUM SPIN SYSTEMS

Ruggero Vaia, Alessandro Cuccoli, Andrea Fubini +1 more

A magnetic system is usually described in terms of the exchange coupling between neighboring spins lying on the sites of a given lattice. Our goal here is to account for the unavoidable quantum effects due to the further coupling with the vibrations of the ions constituting the lattice. A Caldeira-Leggett scheme allows one to treat such effects through the analysis of the associated influence action, obtained after tracing-out the phonons. In a physically sound model, it turns out that one must deal with an environmental coupling which is nonlinear in the system's variables. The corresponding path integral can be dealt with by suitably extending the pure-quantum self-consistent harmonic approximation. In this way one can obtain extended phase diagrams for magnetic phase transitions, accounting for the environmental interaction.

International Conference on Path Integrals•Nov 1, 2008•0 citations

Effective description of the dissipative interaction between simple model-systems and their environment

Dieter Schuch

Chemical reactions are generally connected with energy transfer between reactands and their environment. There are different ways of taking this environment into account. The traditional system-plus-reservoir (S+R) approach couples the relevant system to a large number of environmental degrees of freedom, represented, e.g., by harmonic oscillators. However, this has the disadvantage—from a computational point of view—that a system of many coupled differential equations has to be solved due to the large number of degrees of freedom of the reservoir. The number of degrees of freedom can be drastically reduced if an effective description of the interaction between system and reservoir is applied. On the quantum mechanical level, the effect of the environment can be included, e.g., by the use of explicitly time-dependent Hamiltonians or nonlinear additions to the Schrödinger equation (SE). An advantage of the former method is the preservation of the canonical formalism and the linearity of the theory as well as the fact that its operators can be derived directly from the S+R approach. Therefore, it seems to be even more of a paradox that this method apparently violates the uncertainty principle. This violation does not occur in the nonlinear approaches but the nonlinearity seems, at first sight, to be problematic. However, it can be shown that a particular logarithmic nonlinear SE is equivalent to the approach using the time-dependent Hamiltonian and can be transformed into this. The fact that this transformation is nonunitary provides the key for the solution of the paradox and also allows one to show the equivalence of all three of the above-mentioned approaches. In investigating the classical counterpart, a noncanonical transformation is used between the dissipative physical level and the canonical formal level, which makes it even possible to transform the physical interacting system into a formal isolated system that can be treated in the conventional way. As a result, the effect of the interaction with the environment can be taken into account classically by noncanonical transformations and quantum mechanically by nonunitary transformations. ©1999 John Wiley & Sons, Inc. Int J Quant Chem 72: 537–547, 1999

International Journal of Quantum Chemistry•Jan 1, 1999•29 citations

Analytical solutions for the quantum Brownian motion of a particle during a quantum quench

Ygor de Oliveira Souza, Caio C. Holanda Ribeiro, V. A. De Lorenci

A particle subjected to a fluctuating force originated from its interaction with an external quantum system undergoes quantum Brownian motion. This phenomenon is investigated in detail for the case of a particle confined by a harmonic potential and allowed to interact with a reservoir modeled as a continuum of oscillators, with particular emphasis on transient effects. Assuming a linear coupling between the particle and the reservoir, canonical quantization of the system is implemented, and analytical expressions for the quantum correlations are derived. These correlations are then applied to analyze energy conservation, and the particle Brownian motion is characterized from the perspective of the energy extracted from the reservoir.

arXiv:2501.16611•Jan 28, 2025•0 citations

Unveiling environmental entanglement in strongly dissipative qubits

Soumya Bera, Serge Florens, Harold U. Baranger +3 more

The coupling of a qubit to a macroscopic reservoir plays a fundamental role in understanding the complex transition from the quantum to the classical world. Considering a harmonic environment, we use both intuitive arguments and numerical many-body quantum tomography to study the structure of the complete wavefunction arising in the strong-coupling regime, reached for intense qubit-environment interaction. The resulting strongly-correlated many-body ground state is built from quantum superpositions of adiabatic (polaron-like) and non-adiabatic (antipolaron-like) contributions from the bath of quantum oscillators. The emerging Schrödinger cat environmental wavefunctions can be described quantitatively via simple variational coherent states. In contrast to qubit-environment entanglement, we show that non-classicality and entanglement among the modes in the reservoir are crucial for the stabilization of qubit superpositions in regimes where standard theories predict an effectively classical spin.

arXiv:1301.7430•Jan 30, 2013•1 citation

Non-Markovian effects & decoherence processes in open quantum systems

Graeme Pleasance

This thesis investigates two thematic lines of research, both underpinned by non-Markovian system-reservoir interactions in quantum optics. The overarching focus is on modelling the open system dynamics in a non-perturbative fashion, broadly on - though not restricted to - instances when the environment is structured. A theory is developed by means of enlarging the open system over environmental degrees of freedom to include memory effects in its dynamics. This is achieved using an established technique that involves mapping a bosonic environment onto a 1D chain of harmonic oscillators. Within this setting, we apply a Heisenberg equation-of-motion approach to derive an exact set coupled differential equations for the open system and a single auxiliary oscillator of the chain. The combined equations are shown to have their interpretation rooted in a quantum Markov stochastic process. Including the auxiliary chain oscillator as part of the original system then enables us to obtain an exact master equation for the enlarged system, avoiding any need for the Born-Markov approximations. Our method is valid for a dissipative two-state system, with cases of multiple excitations and added driving discussed. Separately, we apply the framework of quantum Darwinism to an atom-cavity system, and, subsequently, to a more general multiple-environment model. In both cases, the time-dependent spread of correlations between the open system and fractions of the environment is analysed during the course of the decoherence process. The degree to which information is redundant across different fractions is checked to infer the emergence of classicality. In the second case, we go further and present a decomposition of information in terms of its quantum and classical correlations. A quantitative measure of redundancy is also studied with regard to its ability to witness non-Markovian behaviour. Besides fundamental interest, our results have application to quantum information processing and quantum technologies, keeping in mind the potential beneficial use of non-Markovian effects in reservoir engineering.

•Feb 22, 2018•0 citations
The system-plus-reservoir (SPR) model is the most common and effective approach to study quantum dissipative effects. Indeed, it makes quantization possible by considering the whole energy-conserving system, while the reservoir's degrees of freedom, assumed to be harmonic, can be traced out by the path-integral technique, leading to a formulation that only includes the system of interest. In the standard SPR model the environment is only coupled with the system's coordinate and turns out to quench its quantum fluctuations. However, there are physical systems coupled with an environment whose "coordinates" and "momenta" can be completely interchangeable (e.g., magnets), so an SPR coupling must symmetrically affect both canonical variables. In this paper such a general environmental coupling is studied in the case of a harmonic oscillator. It is found that quantum fluctuations are generally enhanced by environmental coupling with an unexpected nonmonotonic behavior. This leads one to speculate about the possibility that spin-lattice coupling could drive the two-dimensional Heisenberg antiferromagnet to reach its quantum-critical point.
The standard system-plus-reservoir approach used in the study of dissipative systems can be meaningfully generalized to a dissipative coupling involving the momentum, instead of the coordinate: the corresponding equation of motion differs from the Langevin equation, so this is called anomalous dissipation. It occurs for systems where such coupling can indeed be derived from the physical analysis of the degrees of freedom that can be treated as a dissipation bath. Starting from the influence functional corresponding to anomalous dissipation, it is shown how to derive the effective classical potential that gives the quantum thermal averages for the dissipative system in terms of classical-like calculations; the generalization to many degrees of freedom is given. The formalism is applied to a single particle in a double well and to the discrete phi(4) model. At variance with the standard case, the fluctuations of the coordinate are enhanced by anomalous dissipative coupling.
A magnetic system is usually described in terms of the exchange coupling between neighboring spins lying on the sites of a given lattice. Our goal here is to account for the unavoidable quantum effects due to the further coupling with the vibrations of the ions constituting the lattice. A Caldeira-Leggett scheme allows one to treat such effects through the analysis of the associated influence action, obtained after tracing-out the phonons. In a physically sound model, it turns out that one must deal with an environmental coupling which is nonlinear in the system's variables. The corresponding path integral can be dealt with by suitably extending the pure-quantum self-consistent harmonic approximation. In this way one can obtain extended phase diagrams for magnetic phase transitions, accounting for the environmental interaction.
Chemical reactions are generally connected with energy transfer between reactands and their environment. There are different ways of taking this environment into account. The traditional system-plus-reservoir (S+R) approach couples the relevant system to a large number of environmental degrees of freedom, represented, e.g., by harmonic oscillators. However, this has the disadvantage—from a computational point of view—that a system of many coupled differential equations has to be solved due to the large number of degrees of freedom of the reservoir. The number of degrees of freedom can be drastically reduced if an effective description of the interaction between system and reservoir is applied. On the quantum mechanical level, the effect of the environment can be included, e.g., by the use of explicitly time-dependent Hamiltonians or nonlinear additions to the Schrödinger equation (SE). An advantage of the former method is the preservation of the canonical formalism and the linearity of the theory as well as the fact that its operators can be derived directly from the S+R approach. Therefore, it seems to be even more of a paradox that this method apparently violates the uncertainty principle. This violation does not occur in the nonlinear approaches but the nonlinearity seems, at first sight, to be problematic. However, it can be shown that a particular logarithmic nonlinear SE is equivalent to the approach using the time-dependent Hamiltonian and can be transformed into this. The fact that this transformation is nonunitary provides the key for the solution of the paradox and also allows one to show the equivalence of all three of the above-mentioned approaches. In investigating the classical counterpart, a noncanonical transformation is used between the dissipative physical level and the canonical formal level, which makes it even possible to transform the physical interacting system into a formal isolated system that can be treated in the conventional way. As a result, the effect of the interaction with the environment can be taken into account classically by noncanonical transformations and quantum mechanically by nonunitary transformations. ©1999 John Wiley & Sons, Inc. Int J Quant Chem 72: 537–547, 1999
A particle subjected to a fluctuating force originated from its interaction with an external quantum system undergoes quantum Brownian motion. This phenomenon is investigated in detail for the case of a particle confined by a harmonic potential and allowed to interact with a reservoir modeled as a continuum of oscillators, with particular emphasis on transient effects. Assuming a linear coupling between the particle and the reservoir, canonical quantization of the system is implemented, and analytical expressions for the quantum correlations are derived. These correlations are then applied to analyze energy conservation, and the particle Brownian motion is characterized from the perspective of the energy extracted from the reservoir.
The coupling of a qubit to a macroscopic reservoir plays a fundamental role in understanding the complex transition from the quantum to the classical world. Considering a harmonic environment, we use both intuitive arguments and numerical many-body quantum tomography to study the structure of the complete wavefunction arising in the strong-coupling regime, reached for intense qubit-environment interaction. The resulting strongly-correlated many-body ground state is built from quantum superpositions of adiabatic (polaron-like) and non-adiabatic (antipolaron-like) contributions from the bath of quantum oscillators. The emerging Schrödinger cat environmental wavefunctions can be described quantitatively via simple variational coherent states. In contrast to qubit-environment entanglement, we show that non-classicality and entanglement among the modes in the reservoir are crucial for the stabilization of qubit superpositions in regimes where standard theories predict an effectively classical spin.
This thesis investigates two thematic lines of research, both underpinned by non-Markovian system-reservoir interactions in quantum optics. The overarching focus is on modelling the open system dynamics in a non-perturbative fashion, broadly on - though not restricted to - instances when the environment is structured. A theory is developed by means of enlarging the open system over environmental degrees of freedom to include memory effects in its dynamics. This is achieved using an established technique that involves mapping a bosonic environment onto a 1D chain of harmonic oscillators. Within this setting, we apply a Heisenberg equation-of-motion approach to derive an exact set coupled differential equations for the open system and a single auxiliary oscillator of the chain. The combined equations are shown to have their interpretation rooted in a quantum Markov stochastic process. Including the auxiliary chain oscillator as part of the original system then enables us to obtain an exact master equation for the enlarged system, avoiding any need for the Born-Markov approximations. Our method is valid for a dissipative two-state system, with cases of multiple excitations and added driving discussed. Separately, we apply the framework of quantum Darwinism to an atom-cavity system, and, subsequently, to a more general multiple-environment model. In both cases, the time-dependent spread of correlations between the open system and fractions of the environment is analysed during the course of the decoherence process. The degree to which information is redundant across different fractions is checked to infer the emergence of classicality. In the second case, we go further and present a decomposition of information in terms of its quantum and classical correlations. A quantitative measure of redundancy is also studied with regard to its ability to witness non-Markovian behaviour. Besides fundamental interest, our results have application to quantum information processing and quantum technologies, keeping in mind the potential beneficial use of non-Markovian effects in reservoir engineering.