The non-Markovian dynamics of open quantum systems is studied from two different points of view. The first one coincides with the traditional tracing out of the environmental degrees of freedom, presented in classical textbooks on open quantum systems. The second one is an approximation of the exact density operator with the knowledge of only several dynamical variables in the spirit of non-equilibrium thermodynamics. The approximation is based on the principle of maximal entropy. We discuss the information and the Renyi entropies, which lead to different approximations. The time-convolutionless master equation governs the dynamics of both traditional and approximated reduced density operator with a particular projection operator. Considering the example of two interacting qubits in a thermal environment, we compare the traditional and thermodynamical approaches.
The non-Markovian dynamics of open quantum systems is studied from two different points of view. The first one coincides with the traditional tracing out of the environmental degrees of freedom, presented in classical textbooks on open quantum systems. The second one is an approximation of the exact density operator with the knowledge of only several dynamical variables in the spirit of non-equilibrium thermodynamics. The approximation is based on the principle of maximal entropy. We discuss the information and the Renyi entropies, which lead to different approximations. The time-convolutionless master equation governs the dynamics of both traditional and approximated reduced density operator with a particular projection operator. Considering the example of two interacting qubits in a thermal environment, we compare the traditional and thermodynamical approaches.
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.
Quantum thermodynamics has emerged as a central field for understanding how energy conversion processes occur in microscopic systems. In these systems, effects such as coherence, entanglement, and non-Markovianity play key roles. In this thesis, we explore different ways to describe quantum thermodynamics, using two main approaches: one based on entropy and the other on ergotropy. First, we introduce a generalized approach to quantify non-Markovianity through the breakdown of monotonicity in thermodynamic functions. In this context, the entropy-based heat flow serves as a practical tool to witness and measure quantum memory in unital maps that do not reverse the sign of the internal energy. Next, we analyze the dynamics of ergotropy in open qubits under both Markovian and non-Markovian evolutions. We identify phenomena such as freezing and sudden death of ergotropy, and we establish an analytical relation between the change in ergotropy and the environment-induced work . This provides a clear physical interpretation for the additional term in the first law in the entropy-based formulation. Finally, we propose an ergotropy-based thermodynamic formulation, in which heat is reinterpreted in terms of the change of the passive state associated with the density operator governing the quantum dynamics. This approach allows one to measure non-Markovianity of unital maps more generally and accurately than the entropy-based heat flow. This advantage comes from the direct link between heat and von Neumann entropy, a property ensured by invariance under passive transformations. Moreover, the out-of-equilibrium temperature naturally remains non-negative, similarly to equilibrium thermodynamics.
Open quantum systems are studied from the thermodynamical point of view unifying the principle of maximum informational entropy and the hypothesis of relaxation times hierarchy. The result of the unification is a non-Markovian and local-in-time master equation that provides a direct connection for dynamical and thermodynamical properties of open quantum systems. The power of the approach is illustrated by the application to the damped harmonic oscillator and the damped driven two-level system, resulting in analytical expressions for the non-Markovian and nonequilibrium entropy and inverse temperature.
In this thesis, we discuss aspects of the simulation, characterisation, and control of the dynamics of open quantum systems. The latter are systems governed by quantum mechanical laws and interacting with an environment, which is typically much larger than the system itself. According to the standard approach, one is usually able to perform a suitable average over the environmental degrees of freedom, resulting in an effective description of the main system dynamics, which accounts for the effects of the interaction with the surroundings. In standard scenarios, usually studied within the so-called Born-Markov approximation, the system-environment coupling is weak and such that we can perform a neat separation of timescales: the environmental dynamics is assumed to be fast compared to the typical evolution timescale of the system of interest. However, nowadays we are able to inspect physical scenarios where the usual Born-Markov approximation breaks down: the interaction between system and environment can be strong, likely leading to non-negligible memory (non-Markovian) effects. In this work, we discuss some instances in which we cannot work in the standard Born-Markov regime. We introduce and analyse some numerical and analytical techniques to characterise and simulate non-standard scenarios. We show that, even in the Markovian regime, the traditional formulation of thermodynamic irreversibility shows flaws and inconsistencies. We thus use phase-space methods to assess the role of initial correlations shared by the two parties of a bipartite harmonic system in the entropy production rate, including non-Markovian effects. Furthermore, we show that certain interactions enable to redraw the boundaries between the system and the environment in an effective manner, resulting in a new picture where the system degrees of freedom are augmented, while the residual environment is rearranged in such a way that the Born-Markov approximation is recovered. This analytical technique, known as reaction coordinate mapping approach, is employed in this work to show that, upon an accurate choice of the parameter regime, a spin-boson model can serve as a quantum analogue simulator of non-Markovian multiphoton Jaynes-Cummings models. These systematic studies shed light on the thermodynamic characterisation of open quantum systems, as well as on their numerical simulation.
We study the role of correlations with the environment as the source of non-Markovian quantum evolutions. We first focus on the impact that correlations with the environment can have on the dynamical map that evolve the system. We expand the set of initial states of a system and its environment that are known to guarantee completely positive reduced dynamics for the system when the combined state evolves unitarily. We characterize the correlations in the initial state in terms of its quantum discord. The induced maps can be not completely positive when quantum correlations including, but not limited to, entanglement are present. We discuss the implications and limitations of the Markov approximation necessary to derive the Kossakowski-Lindblad master equation. A generalized non-Markovian master equation is derived from the dynamical map of systems correlated with their environment. The physical meaning of not completely positive maps is studied to obtain a consistent theory of non-Markovian quantum dynamics. These are associated to inverse maps necessary to establish correlations and they give rise to a canonical embedding map that is local in time. This master equation goes beyond the Kossakowski-Lindblad master equation. Non-equilibrium quantum thermodynamics can be be studied within this theory. Through out this discussion, the general dynamics of two interacting qubits is used as an example for illustrations.
The dynamics of finite dimension open quantum systems is studied with the help of the simplest possible form of projection operators, namely the ones which project only onto one-dimensional subspaces. The simplicity of the action of the projection operators always leads to an analytical solution of the dynamical master equation, even in the non-Markovian case, in any perturbative order. The analytical solution correctly reproduces the short-time dynamics, and can be used to recursively recover the dynamics for an arbitrary time interval with arbitrary precision. The necessary number of relevant degrees of freedom to completely characterise an open quantum system is ( n − 1 ) ( n + 2 ) / 2 , where n is the dimension of the Hilbert space of the open system. The method is illustrated by two examples, the relaxation of a qubit in a thermal bath and the dynamics of two interacting qubits in a common environment.