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:2607.08655

Temperature Beyond Equilibrium in Isolated Quantum Many-Body Systems and Their Subsystems

Maurizio Fagotti

quant-phcond-mat.stat-mechmath-phSubmitted Jul 9, 2026• Announced Jul 10, 2026• 0 citations• Revised Oct 20, 2026 (v3)
v1 · Jul 9, 2026v2 · Jul 30, 2026v3 · Oct 20, 2026
arXivHTMLPDF

Abstract

Temperature is one of the central concepts of thermodynamics, yet its meaning far from equilibrium remains unclear. The problem is especially challenging in isolated quantum many-body systems, whose states evolve unitarily, may remain far from equilibrium, and retain energy coherence, a genuinely quantum feature with no direct classical counterpart. Specifically, energy fluctuations in a nonstationary quantum state have two distinct origins. Part of these fluctuations comes from uncertainty in the energy populations and has the usual thermodynamic meaning. The rest comes from quantum coherence between energy sectors and is responsible for the state's time dependence. We propose that, even away from equilibrium, temperature identifies the state within the family of regular states sharing the same energy-coherence structure. The resulting inverse temperature is obtained from a principle of minimum discrimination information, which selects the least distinguishable state compatible with the prescribed energy and coherence structure. This replaces the usual maximum-entropy principle, which, applied naively, can yield a biased estimator of the inverse temperature. We also lay the groundwork for an extension of the construction to subsystems and show that, although the inverse temperature of a subsystem is not determined by its reduced state alone, under an alignment assumption, its instantaneous rate of change is a local quantity for sufficiently large subsystems.

Comments
28 pages, 5 figures

Related papers

Thermodynamics Beyond Equilibrium in Coherent Quantum Systems

Md Manirul Ali, Po-Wen Chen

A central open question in quantum thermodynamics is the identification of thermodynamic entropy away from equilibrium. Although thermodynamic entropy coincides with the von Neumann entropy for a Gibbs state at equilibrium, the thermodynamic role of quantum coherence generated during nonequilibrium evolution remains unclear. Here, we show that von Neumann entropy does not, in general, represent the thermodynamic entropy governing heat exchange in coherent nonequilibrium quantum systems. By integrating the resource theory of quantum coherence with thermodynamic principles, we develop a general framework for nonequilibrium quantum thermodynamics. We identify thermodynamic entropy with the energy entropy derived from energy-measurement statistics and introduce a dynamical temperature extending the equilibrium concept to nonequilibrium states. Consequently, we obtain an exact entropy-balance relation separating the entropy flux associated with heat exchange from the coherence-loss contribution to entropy production, establishing an operational connection between quantum coherence, heat flow, and total entropy change. Unlike approaches relying on equilibrium reference states or stationary Gibbs ensembles, our framework uses instantaneous dynamical quantities and remains valid throughout transient nonequilibrium evolution. It provides consistent dynamical definitions of temperature, work, heat, and free energy. Applying the formalism to an exactly solvable open quantum system, we show that the first and second laws hold throughout transient evolution and that equilibrium thermodynamics emerges dynamically in the weak-coupling long-time limit. Our results establish a unified framework for coherent nonequilibrium quantum thermodynamics and suggest opportunities for controlling heat dissipation through coherence engineering in quantum thermal technologies.

quant-pharXiv:2602.09074•APL Quantum•Feb 10, 2026•0 citations

Emergence of Thermodynamics from Equilibration in Isolated Quantum Systems

Adalberto D. Varizi, Daniel Jonathan, Thiago R. de Oliveira

Understanding how macroscopic thermodynamic behavior emerges from microscopic quantum dynamics remains an open problem. While equilibration of quantum observables is well established, thermodynamics also relies on variables not directly associated with linear operators, but which are defined instead as functions of expectation values. Whether and how such derived quantities inherit equilibration properties is an open question. Here, we establish that any continuously differentiable function of equilibrating expectation values also equilibrates. We apply this result to a bipartite isolated system, showing that the entropy and conjugate variables of each subsystem -- defined through Jaynes' maximum entropy principle -- equilibrate. Moreover, with the assumption that their equilibrium properties depend solely on local conserved quantities, we show the dynamical maximization of the total entropy, enforcing equality of conjugate variables across subsystems. These results provide a direct dynamical justification for entropy maximization and the emergence of thermodynamic equilibrium conditions, showing that fundamental principles of thermodynamics follow from the unitary evolution of quantum systems.

quant-pharXiv:2606.28660•Jun 30, 2026•0 citations

Work, entropy and uncertainties in thermodynamics beyond the classical and weak coupling regime

Harry J. D. Miller

Thermodynamics typically concerns the physical behaviour of macroscopic systems comprised of many particles. However, recent theoretical progress has extended the theory to both the classical-stochastic and quantum regimes, where systems are comprised of just a small number of particles. In this thesis I investigate a range of situations in which new thermodynamic phenomena emerge due to the reduced size of the systems involved. One central assumption in macroscopic thermodynamics is the weak coupling approximation, which posits that the equilibrium properties of a system are not influenced by the interactions with its surrounding environment. However, for microscopic systems this assumption can break down, and I derive new fluctuation relations that provide a refined form of the second law of thermodynamics in this strong-coupling regime, taking into account corrections stemming from these interactions. In this work I provide a characterisation of stochastic heat and entropy production for small scale classical systems that are defined regardless of the strength of interaction. I then show that these definitions lead to a consistent thermodynamic framework valid beyond the usual weak-coupling regime. The thesis also concerns the effect of interactions on the equilibrium properties of strongly-coupled quantum systems, and I investigate how these interactions can influence the resulting temperature fluctuations in this regime. Using tools from quantum estimation theory, I derive an uncertainty relation between energy and temperature valid at all coupling strengths and system sizes. The relation reveals how quantum energy coherences contribute to statistical fluctuations in the estimated temperature of small- scale systems. Finally, I investigate how quantum fluctuations influence the statistics of work extracted from slowly-driven quantum systems. I prove that, unlike in classical systems, the work dissipated by a general quantum system is no longer proportional to its statistical fluctuations. This result reveals new subtleties involved in designing optimal quantum thermodynamic processes.

•Aug 19, 2019•0 citations

First and Second Law of Quantum Thermodynamics: A Consistent Derivation Based on a Microscopic Definition of Entropy

Philipp Strasberg, Andreas Winter

Deriving the laws of thermodynamics from a microscopic picture is a central quest of statistical mechanics.This tutorial focuses on the derivation of the first and second law for isolated and open quantum systems far from equilibrium, where such foundational questions also become practically relevant for emergent nanotechnologies.The derivation is based on a microscopic definition of five essential quantities: internal energy, thermodynamic entropy, work, heat, and temperature.These definitions are shown to satisfy the phenomenological laws of nonequilibrium thermodynamics for a large class of states and processes.The consistency with previous results is demonstrated.The framework applies to multiple baths including particle transport and accounts for processes with, e.g., a changing temperature of the bath, which is determined microscopically.An integral fluctuation theorem for entropy production is satisfied.In summary, this tutorial introduces a consistent and versatile framework to understand and apply the laws of thermodynamics in the quantum regime and beyond.

arXiv:2002.08817•PRX Quantum•Aug 19, 2021•129 citations

Temperature uncertainty relation in non-equilibrium thermodynamics

Ning Zhang, Si‐Yuan Bai, Chong Chen

Temperature uncertainty of a quantum system in canonical ensemble is inversely determined by its energy fluctuation, which is known as the temperature-energy uncertainty relation. No such uncertainty relation was discovered for a non-equilibrium open quantum system. In this article, we derive a universal temperature uncertainty relation for general non-equilibrium processes. We find that it is the fluctuation of heat, which is defined as the change in bath energy, determines the temperature uncertainty in non-equilibrium case. Specifically, the heat is divided into trajectory heat and backaction heat, which are associated with the system's trajectory of evolution and the backaction of partial measurement on system, respectively. Based on this decomposition, we reveal that both correlations between system and bath's process function and state function are the resources for enhancing temperature precision. Our findings are conductive to design ultrahigh sensitive quantum thermometer.

arXiv:2204.10044•Apr 21, 2022•0 citations

Finite-time quantum equilibration from local correlations

Piotr Ćwikliński

An isolated quantum system evolves reversibly, yet a small subsystem can lose nearly all information about its initial state. Conserved quantities may retain some of this information, depending on how strongly they overlap with local observables. Here we consider a subsystem in an arbitrary initial state coupled to a maximally mixed bath. We show that the worst-input mean-square equilibration error, maximised over window origins, is bounded from above and below by the mean square of a complete local autocorrelation, with the stationary part subtracted. The two mean-square quantities are linearly comparable. A correlation record over a finite interval therefore controls the equilibration error in every interval of the same length, and the result extends to nonnegative observation weights with nonnegative Fourier transform. The result allows arbitrary degeneracies of energies and gaps. We apply it to two static Hamiltonian families. For fixed spin subsystems in the one-particle sector of a bounded-range periodic clock, fixed-accuracy thermalisation is guaranteed on windows that grow only slightly faster than linearly with system size, despite exponentially small positive energies. A random commuting model with logarithmic interaction range retains an extensive set of conserved observables. Its expected mean-square error is bounded by a finite-size term and an inverse-time term. The inverse-time dependence is unavoidable because of the initial transient. These examples show how local relaxation can coexist with exact conservation laws and a finely spaced spectrum.

quant-pharXiv:2610.16351•Oct 13, 2026•0 citations
Temperature is one of the central concepts of thermodynamics, yet its meaning far from equilibrium remains unclear. The problem is especially challenging in isolated quantum many-body systems, whose states evolve unitarily, may remain far from equilibrium, and retain energy coherence, a genuinely quantum feature with no direct classical counterpart. Specifically, energy fluctuations in a nonstationary quantum state have two distinct origins. Part of these fluctuations comes from uncertainty in the energy populations and has the usual thermodynamic meaning. The rest comes from quantum coherence between energy sectors and is responsible for the state's time dependence. We propose that, even away from equilibrium, temperature identifies the state within the family of regular states sharing the same energy-coherence structure. The resulting inverse temperature is obtained from a principle of minimum discrimination information, which selects the least distinguishable state compatible with the prescribed energy and coherence structure. This replaces the usual maximum-entropy principle, which, applied naively, can yield a biased estimator of the inverse temperature. We also lay the groundwork for an extension of the construction to subsystems and show that, although the inverse temperature of a subsystem is not determined by its reduced state alone, under an alignment assumption, its instantaneous rate of change is a local quantity for sufficiently large subsystems.
A central open question in quantum thermodynamics is the identification of thermodynamic entropy away from equilibrium. Although thermodynamic entropy coincides with the von Neumann entropy for a Gibbs state at equilibrium, the thermodynamic role of quantum coherence generated during nonequilibrium evolution remains unclear. Here, we show that von Neumann entropy does not, in general, represent the thermodynamic entropy governing heat exchange in coherent nonequilibrium quantum systems. By integrating the resource theory of quantum coherence with thermodynamic principles, we develop a general framework for nonequilibrium quantum thermodynamics. We identify thermodynamic entropy with the energy entropy derived from energy-measurement statistics and introduce a dynamical temperature extending the equilibrium concept to nonequilibrium states. Consequently, we obtain an exact entropy-balance relation separating the entropy flux associated with heat exchange from the coherence-loss contribution to entropy production, establishing an operational connection between quantum coherence, heat flow, and total entropy change. Unlike approaches relying on equilibrium reference states or stationary Gibbs ensembles, our framework uses instantaneous dynamical quantities and remains valid throughout transient nonequilibrium evolution. It provides consistent dynamical definitions of temperature, work, heat, and free energy. Applying the formalism to an exactly solvable open quantum system, we show that the first and second laws hold throughout transient evolution and that equilibrium thermodynamics emerges dynamically in the weak-coupling long-time limit. Our results establish a unified framework for coherent nonequilibrium quantum thermodynamics and suggest opportunities for controlling heat dissipation through coherence engineering in quantum thermal technologies.
Understanding how macroscopic thermodynamic behavior emerges from microscopic quantum dynamics remains an open problem. While equilibration of quantum observables is well established, thermodynamics also relies on variables not directly associated with linear operators, but which are defined instead as functions of expectation values. Whether and how such derived quantities inherit equilibration properties is an open question. Here, we establish that any continuously differentiable function of equilibrating expectation values also equilibrates. We apply this result to a bipartite isolated system, showing that the entropy and conjugate variables of each subsystem -- defined through Jaynes' maximum entropy principle -- equilibrate. Moreover, with the assumption that their equilibrium properties depend solely on local conserved quantities, we show the dynamical maximization of the total entropy, enforcing equality of conjugate variables across subsystems. These results provide a direct dynamical justification for entropy maximization and the emergence of thermodynamic equilibrium conditions, showing that fundamental principles of thermodynamics follow from the unitary evolution of quantum systems.
Thermodynamics typically concerns the physical behaviour of macroscopic systems comprised of many particles. However, recent theoretical progress has extended the theory to both the classical-stochastic and quantum regimes, where systems are comprised of just a small number of particles. In this thesis I investigate a range of situations in which new thermodynamic phenomena emerge due to the reduced size of the systems involved. One central assumption in macroscopic thermodynamics is the weak coupling approximation, which posits that the equilibrium properties of a system are not influenced by the interactions with its surrounding environment. However, for microscopic systems this assumption can break down, and I derive new fluctuation relations that provide a refined form of the second law of thermodynamics in this strong-coupling regime, taking into account corrections stemming from these interactions. In this work I provide a characterisation of stochastic heat and entropy production for small scale classical systems that are defined regardless of the strength of interaction. I then show that these definitions lead to a consistent thermodynamic framework valid beyond the usual weak-coupling regime. The thesis also concerns the effect of interactions on the equilibrium properties of strongly-coupled quantum systems, and I investigate how these interactions can influence the resulting temperature fluctuations in this regime. Using tools from quantum estimation theory, I derive an uncertainty relation between energy and temperature valid at all coupling strengths and system sizes. The relation reveals how quantum energy coherences contribute to statistical fluctuations in the estimated temperature of small- scale systems. Finally, I investigate how quantum fluctuations influence the statistics of work extracted from slowly-driven quantum systems. I prove that, unlike in classical systems, the work dissipated by a general quantum system is no longer proportional to its statistical fluctuations. This result reveals new subtleties involved in designing optimal quantum thermodynamic processes.
Deriving the laws of thermodynamics from a microscopic picture is a central quest of statistical mechanics.This tutorial focuses on the derivation of the first and second law for isolated and open quantum systems far from equilibrium, where such foundational questions also become practically relevant for emergent nanotechnologies.The derivation is based on a microscopic definition of five essential quantities: internal energy, thermodynamic entropy, work, heat, and temperature.These definitions are shown to satisfy the phenomenological laws of nonequilibrium thermodynamics for a large class of states and processes.The consistency with previous results is demonstrated.The framework applies to multiple baths including particle transport and accounts for processes with, e.g., a changing temperature of the bath, which is determined microscopically.An integral fluctuation theorem for entropy production is satisfied.In summary, this tutorial introduces a consistent and versatile framework to understand and apply the laws of thermodynamics in the quantum regime and beyond.
Temperature uncertainty of a quantum system in canonical ensemble is inversely determined by its energy fluctuation, which is known as the temperature-energy uncertainty relation. No such uncertainty relation was discovered for a non-equilibrium open quantum system. In this article, we derive a universal temperature uncertainty relation for general non-equilibrium processes. We find that it is the fluctuation of heat, which is defined as the change in bath energy, determines the temperature uncertainty in non-equilibrium case. Specifically, the heat is divided into trajectory heat and backaction heat, which are associated with the system's trajectory of evolution and the backaction of partial measurement on system, respectively. Based on this decomposition, we reveal that both correlations between system and bath's process function and state function are the resources for enhancing temperature precision. Our findings are conductive to design ultrahigh sensitive quantum thermometer.
An isolated quantum system evolves reversibly, yet a small subsystem can lose nearly all information about its initial state. Conserved quantities may retain some of this information, depending on how strongly they overlap with local observables. Here we consider a subsystem in an arbitrary initial state coupled to a maximally mixed bath. We show that the worst-input mean-square equilibration error, maximised over window origins, is bounded from above and below by the mean square of a complete local autocorrelation, with the stationary part subtracted. The two mean-square quantities are linearly comparable. A correlation record over a finite interval therefore controls the equilibration error in every interval of the same length, and the result extends to nonnegative observation weights with nonnegative Fourier transform. The result allows arbitrary degeneracies of energies and gaps. We apply it to two static Hamiltonian families. For fixed spin subsystems in the one-particle sector of a bounded-range periodic clock, fixed-accuracy thermalisation is guaranteed on windows that grow only slightly faster than linearly with system size, despite exponentially small positive energies. A random commuting model with logarithmic interaction range retains an extensive set of conserved observables. Its expected mean-square error is bounded by a finite-size term and an inverse-time term. The inverse-time dependence is unavoidable because of the initial transient. These examples show how local relaxation can coexist with exact conservation laws and a finely spaced spectrum.