We investigate the non-equilibrium thermodynamics of pure decoherence. In a pure decoherence process, the system Hamiltonian is a constant of motion and there is no direct energy exchange between the system and its surroundings. Nevertheless, the environment’s energy is not generally conserved and in this work we show that this leads to non-trivial heat dissipation as a result of decoherence alone. This heat has some very distinctive properties: it obeys an integral fluctuation relation and can be interpreted in terms of the entropy production associated with populations in the energy eigenbasis of the initial state. We show that the heat distribution for a pure decoherence process is different from the distribution of work done by the initial system–bath interaction quench. Instead, it corresponds to a mixture of work distributions of cyclical processes, each conditioned on a state of the open system. Inspired by recent experiments on impurities in ultracold gases, we demonstrate our general results by studying the heat generated by the decoherence of a qubit immersed within a degenerate Fermi gas in the lowest band of a species-selective optical lattice.
We investigate the non-equilibrium thermodynamics of pure decoherence. In a pure decoherence process, the system Hamiltonian is a constant of motion and there is no direct energy exchange between the system and its surroundings. Nevertheless, the environment’s energy is not generally conserved and in this work we show that this leads to non-trivial heat dissipation as a result of decoherence alone. This heat has some very distinctive properties: it obeys an integral fluctuation relation and can be interpreted in terms of the entropy production associated with populations in the energy eigenbasis of the initial state. We show that the heat distribution for a pure decoherence process is different from the distribution of work done by the initial system–bath interaction quench. Instead, it corresponds to a mixture of work distributions of cyclical processes, each conditioned on a state of the open system. Inspired by recent experiments on impurities in ultracold gases, we demonstrate our general results by studying the heat generated by the decoherence of a qubit immersed within a degenerate Fermi gas in the lowest band of a species-selective optical lattice.
We study the nonequilibrium thermodynamics of pure decoherence processes in open quantum systems coupled to a thermal reservoir. We review various definitions of central quantities, such as internal energy, work, heat, and entropy production, developed within local and global approaches to quantum thermodynamics. Within local approaches, thermodynamic quantities only refer to the open system's degrees of freedom, while in the global approaches, certain quantities are defined by referring explicitly to the reservoir degrees of freedom. Employing a microscopic, analytically solvable model, we perform a comparison of these two perspectives, revealing substantial differences in the thermodynamic quantities and in the formulations of the first and second laws. The main reason for these discrepancies is the fact that the global approaches involve the system-reservoir interaction which exchanges a large amount of energy with the environment, while the average open system energy is constant in time because the dynamics represents pure decoherence and does not affect the open system populations.
A consistent theory of non-equilibrium thermodynamics for Markovian open quantum systems has been developed in the late seventies in analogy with Classical Irreversible Thermodynamics. The time-evolution of these open systems is usually described by means of effective master equations in Lindblad form, that turn out to be reliable when there is a separation of time-scales between system and environment, such that memory effects are negligible and the so-called Markovian approximation is justified. In this framework, the variations of energy and entropy in the system are consistently described, distinguishing between heat and work contributions and providing a statement of the second law of thermodynamics as positivity of the entropy production.\nHowever, there is empirical evidence that many physical systems like photosynthetic complexes,\nopto-mechanical resonators and superconducting qubits, just to mention a few, experience more general non-Markovian dynamics. The formulation of the laws of thermodynamics in a non-Markovian setting is matter of current research and represents the main topic of the present work. As a first step, we show that the entropy production defined as in the Markovian case can be negative for a class of non-Markovian dynamics. We argue that this outcome should not be interpreted as a violation of the second law of thermodynamics because the environment must be explicitly taken into account in the balance of entropy in the non-Markovian setting. In order to justify this claim we adopt a more general point of view, studying a closed bipartite quantum system, such that each of the two subsystems plays the role of a finite environment out of equilibrium for the other one. We concentrate on the balance of energy first and construct an effective Hamiltonian for each subsystem using physically reasonable requirements; then we define heat and work as in the standard Markovian treatment, with the effective Hamiltonian replacing the free Hamiltonian. It turns out that, in our framework, the work power is perfectly balanced between subsystems, while the correlations can store a part of energy locally inaccessible and exchange it with both subsystems in the form of heat.\nConcerning the balance of entropy, a quite general formulation of the second law of thermodynamics can be given as follows: under the assumption of a factorized initial state for the compound system, the sum of the total variations of the entropies in the two subsystems is always nonnegative. We show with an explicit example that this general formulation does not correspond to the statement presented in the framework of Markovian master equations, which should not be considered a priori the second law of thermodynamics.\nIn the last part of the thesis we concentrate of the so-called fluctuation relations, that are results extending the thermodynamic formalism beyond the behavior of average quantities. After reviewing the main theoretical outcomes, such as the Jarzynski equality and the Crooks fluctuation theorem, we describe a proposal to access experimentally the work performed on an ensemble of diatomic molecules by a time-dependent electric field coupled with their vibrational degree of freedom. This procedure could then be used to test the quantum Jarzynski equality. With respect to the results so far appeared in the literature, in which the left-hand side of the equality is inferred from an experiment and the right-hand side is computed according to a model, in our proposed setting we should be able to estimate from the experiment both the left-hand side and the right-hand side of the equality, independently.
How quantum coherence influences thermodynamic behavior remains an open question in quantum thermodynamics. Here we investigate this relation within the pure dephasing framework, where a central qubit interacts with a finite Ising-like spin environment. Although the system's internal energy remains constant, the interaction induces decoherence and gives rise to nontrivial thermodynamic features. Within the two-point measurement approach, we show that the heat dissipated into the environment matches the coherent energy contribution appearing in a reformulated first law of quantum thermodynamics. Numerical calculations reveal oscillatory coherence dynamics, with revivals associated with information backflow and non-Markovian effects, as quantified by the Breuer-Laine-Piilo measure. We find that heat and coherence exhibit intertwined temporal behavior, with enhanced heat dissipation during coherence decay and reduced heat during revivals. These results suggest a connection between coherence dynamics and thermodynamic quantities in finite, closed composite systems undergoing pure dephasing.
Thermodynamics is a phenomenological theory describing the energy conversion of work and heat. At its origins thermodynamics was developed in order to understand and improve heat engines. In conventional thermodynamics, however, only such processes are completely describable which are slow enough to keep the system of interest in an equilibrium state with its thermal environment at all times. On the contrary, all real physical processes are accompanied by non-equilibrium phenomena. These are mathematically described with the help of the irreversible entropy production, i.e. the dissipated work divided by the temperature of the bath. The second law of thermodynamics merely states that the irreversible entropy production is on average always positive. The modern trend of miniaturization, however, leads to smaller and smaller devices. On short length scales thermal noise as well as quantum fluctuations become important. Thus, usual thermodynamic quantities as work and heat acquire stochastic nature. Moreover, in the quantum regime a completely new theory had to be invented, since classical notions of work and heat are no longer valid. The present dissertation contributes to this prevailing field by the derivation of analytical expressions for the entropy production in open and closed quantum system far from thermal equilibrium. The theoretical treatment is motivated by an experimental point of view. The obtained results were derived from the reduced dynamics of the quantum mechanical system, which may be coupled to a thermal bath. To this end, it was dealt with methods and approaches of statistical physics, conventional thermodynamics, quantum information theory and the theory of open quantum systems. In this dissertation the most important physical systems are treated. First, an isolated system is considered before later on a heat bath is included. The limit of weak as well as of strong coupling are analyzed in detail. For isolated systems it turns out that a geometric approach is able to capture the thermodynamic properties, completely. To this end, the irreversible entropy production is sharply estimated from below by the angle between the real non-equilibrium state and the corresponding equilibrium one. Further, it is shown that the Heisenberg uncertainty relation for energy and time can be formulated more precisely in terms of that angle. As experimental system cold ion traps are introduced, in which the theoretical predictions can be verified. For weakly coupled systems, then, the irreversible entropy production is identified and a fluctuation theorem is derived by merely thermodynamic arguments. As experimental system we, again, propose the cold ion traps, where the heat bath can be simulated with the help of LASER light. In the limit of strong coupling a semiclassical description of the reduced quantum system is discussed. Again, an analytically exact expression for the entropy production and the corresponding fluctuation theorem is derived. A physical system, in which strong coupling to the environment can be analyzed, is given by Josephson junctions. This dissertation discusses the entropy production for isolated, weakly coupled, and overdamped quantum systems. For these physical regimes analytical relation are derived and experimental systems proposed, with which the predictions can be verified.
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.
Abstract We consider quantum decoherence and Landauer’s principle in qubit-cavity quantum field theory (QFT) interaction, treating the qubit as the system and cavity QFT as the environment. In particular, we investigate the changes that occur in the system with a pure initial state and environment during the decoherence process, with or without energy dissipation, and compare the results with the case in which the initial state of the system is a mixed state and thus decoherence is absent. When we choose an interaction Hamiltonian such that the energy and coherence of the system change simultaneously, the population change of the system and the energy change are the same when the initial state is mixed. However, the decoherence terms increase the von Neumann entropy of the system. In this case the energy change and decoherence of the system are not independent physical processes. The decoherence process maintains unitarity. On the other hand, if the interaction Hamiltonian does not change the energy of the system, there is only the decoherence effect. The environment will be a distribution in the basis of the displaced number state and always increases the energy. Landauer’s principle is satisfied in both cases.