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Authors
R. Tsekov
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A new discrete model for energy relaxation of a quantum particle is described via a projection operator, causing the wave function collapse. Power laws for the evolution of the particle coordinate and momentum dispersions are derived. A new dissipative Schrodinger equation is proposed and solved for particular cases. A new dissipative Liouville equation is heuristically constructed.
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Thermodynamics is a theory of equilibrium transformations, but quantum dynamics are inherently out-of-equilibrium. It remains an open problem to show how the two theories are consistent with each other. Here we extend the ideas of pure state quantum statistical mechanics to show the equilibration of isolated quantum processes; that most multitime observables cannot distinguish a nonequilibrium process from an equilibrium one, unless the system is probed for an extremely large number of times. A surprising corollary of our results is that the size of non-Markovianity and other characteristics of the nonequilibrium process are bounded by that of the equilibrium process.
We investigate the time evolution of an open quantum system described by a Lindblad master equation with dissipation acting only on a part of the degrees of freedom ${cal H}_0$ of the system, and targeting a unique dark state in ${cal H}_0$. We show that, in the Zeno limit of large dissipation, the density matrix of the system traced over the dissipative subspace ${cal H}_0$, evolves according to another Lindblad dynamics, with renormalized effective Hamiltonian and weak effective dissipation. This behavior is explicitly checked in the case of Heisenberg spin chains with one or both boundary spins strongly coupled to a magnetic reservoir. Moreover, the populations of the eigenstates of the renormalized effective Hamiltonian evolve in time according to a classical Markov dynamics. As a direct application of this result, we propose a computationally-efficient exact method to evaluate the nonequilibrium steady state of a general system in the limit of strong dissipation.
Irreversibility is a fundamental concept with important implications at many levels. It pinpoints the fundamental difference between the intrinsically reversible microscopic equations of motion and the unidirectional arrow of time that emerges at the macroscopic level. More pragmatically, a full quantification of the degree of irreversibility of a given process can help in the characterisation of the performance of thermo-machines operating at the quantum level. Here, we review the concept of entropy production, which is commonly intended as {it the} measure of thermodynamic irreversibility of a process, pinpointing the features and shortcomings of its current formulation.
The dissipation generated during a quasistatic thermodynamic process can be characterised by introducing a metric on the space of Gibbs states, in such a way that minimally-dissipating protocols correspond to geodesic trajectories. Here, we show how to generalize this approach to open quantum systems by finding the thermodynamic metric associated to a given Lindblad master equation. The obtained metric can be understood as a perturbation over the background geometry of equilibrium Gibbs states, which is induced by the Kubo-Mori-Bogoliubov (KMB) inner product. We illustrate this construction on two paradigmatic examples: an Ising chain and a two-level system interacting with a bosonic bath with different spectral densities.
One of the general mechanisms that give rise to the slow cooperative relaxation characteristic of classical glasses is the presence of kinetic constraints in the dynamics. Here we show that dynamical constraints can similarly lead to slow thermalization and metastability in translationally invariant quantum many-body systems. We illustrate this general idea by considering two simple models: (i) a one-dimensional quantum analogue to classical constrained lattice gases where excitation hopping is constrained by the state of neighboring sites, mimicking excluded-volume interactions of dense fluids; and (ii) fully packed quantum dimers on the square lattice. Both models have a Rokhsar--Kivelson (RK) point at which kinetic and potential energy constants are equal. To one side of the RK point, where kinetic energy dominates, thermalization is fast. To the other, where potential energy dominates, thermalization is slow, memory of initial conditions persists for long times, and separation of timescales leads to pronounced metastability before eventual thermalization. Furthermore, in analogy with what occurs in the relaxation of classical glasses, the slow-thermalization regime displays dynamical heterogeneity as manifested by spatially segregated growth of entanglement.
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