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arXiv:1609.03885 · Physical review. E

Nonequilibrium quantum chains under multisite Lindblad baths

Pedro H. Guimarães, Gabriel Teixeira Landi, Mário J. de Oliveira

Published Sep 30, 2016• 47 citations
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Abstract

We study a quantum XX chain coupled to two heat reservoirs that act on multiple sites and are kept at different temperatures and chemical potentials. The baths are described by Lindblad dissipators, which are constructed by direct coupling to the fermionic normal modes of the chain. Using a perturbative method, we are able to find analytical formulas for all steady-state properties of the system. We compute both the particle or magnetization current and the energy current, both of which are found to have the structure of Landauer's formula. We also obtain exact formulas for the Onsager coefficients. All properties are found to differ substantially from those of a single-site bath. In particular, we find a strong dependence on the intensity of the bath couplings. In the weak-coupling regime, we show that the Onsager reciprocal relations are satisfied.

DOI
10.1103/physreve.94.032139

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We study a quantum XX chain coupled to two heat reservoirs that act on multiple sites and are kept at different temperatures and chemical potentials. The baths are described by Lindblad dissipators, which are constructed by direct coupling to the fermionic normal modes of the chain. Using a perturbative method, we are able to find analytical formulas for all steady-state properties of the system. We compute both the particle or magnetization current and the energy current, both of which are found to have the structure of Landauer's formula. We also obtain exact formulas for the Onsager coefficients. All properties are found to differ substantially from those of a single-site bath. In particular, we find a strong dependence on the intensity of the bath couplings. In the weak-coupling regime, we show that the Onsager reciprocal relations are satisfied.
Quantum master equations form an important tool in the description of transport problems in open quantum systems. However, they suffer from the difficulty that the shape of the Lindblad dissipator depends sensibly on the system Hamiltonian. Consequently, most of the work done in this field has focused on phenomenological dissipators which act locally on different parts of the system. In this paper we show how to construct Lindblad dissipators to model a one-dimensional bosonic tight-binding chain connected to two baths at the first and last site, kept at different temperatures and chemical potentials. We show that even though the bath coupling is local, the effective Lindblad dissipator stemming from this interaction is inherently nonlocal, affecting all normal modes of the system. We then use this formalism to study the current of particles and energy through the system and find that they have the structure of Landauer's formula, with the bath spectral density playing the role of the transfer integral. Finally, we consider infinitesimal temperature and chemical potential gradients and show that the currents satisfy Onsager's reciprocal relations, which is a consequence of the fact that the microscopic quantum dynamics obeys detailed balance.
We propose a model of nonequilibrium quantum transport of particles and energy in a system connected to mesoscopic Fermi reservoirs (mesoreservoir). The mesoreservoirs are in turn thermalized to prescribed temperatures and chemical potentials by a simple dissipative mechanism described by the Lindblad equation. As an example, we study transport in monoatomic and diatomic chains of noninteracting spinless fermions. We show numerically the breakdown of the Onsager reciprocity relation due to the dissipative terms of the model.
In this thesis we develop a systematic formalism that allows the calculation of transport properties for small quantum systems coupled to multiple baths with different temperatures and/or chemical potentials. Our approach is based on a generalization of the projector operator technique, previously used to study the evolution towards equilibrium of systems weakly coupled to a single bath. Applying this technique to a system weakly coupled to multiple baths, we find a dynamical equation for the reduced density matrix of the system (the reduced density matrix is obtained by tracing out from the total density matrix the baths’ degrees of freedom). Integration of this dynamical equation gives the time evolution of the biased system. After a time interval long enough compared to the characteristic time-scales of the problem, the system arrives to a non-equilibrium steady-state. The density matrix in this non-equilibrium steady state can also be calculated directly, avoiding the time-integration of the dynamical equation. In the second part of the thesis we study non-equilibrium steady states and heat transport through short spin chains coupled to two thermal baths with different temperature. Two new definitions for the local temperature in nonequilibrium are proposed, based on local spin and energy at different sites. The definition based on the local energy seems to be more reliable. We find that for small biases, the heat and spin currents increase proportionally to the bias, however non-linear behavior is observed for large biases. The temperature profile of the chain depends strongly on the parameters of the system.
We study the steady state of a finite XX chain coupled at its boundaries to quantum reservoirs made of free spins that interact one after the other with the chain. The two-point correlations are calculated exactly, and it is shown that the steady state is completely characterized by the magnetization profile and the associated current. Except at the boundary sites, the magnetization is given by the average of the reservoirs' magnetizations. The steady-state current, proportional to the difference in the reservoirs' magnetizations, shows a nonmonotonic behavior with respect to the system-reservoir coupling strength, with an optimal current state for a finite value of the coupling. Moreover, we show that the steady state can be described by a generalized Gibbs state.
We obtain exact formulas for the time-dependence of a few physical observables for the open XX spin chain with Lindbladian dynamics. Our analysis is based on the fact that the Lindblad equation for an arbitrary open quadratic system of N N fermions is explicitly solved in terms of diagonalization of a 4N\times4N 4 N × 4 N matrix called structure matrix by following the scheme of the third quantization. We mainly focus on the time-dependence of magnetization and spin current. As a short-time behavior at a given site, we observe the plateau regime except near the center of the chain. Basic features of this are explained by the light-cone structure created by propagations of boundary effects from the initial time, but we can explain their more detailed properties analytically using our exact formulas. On the other hand, after the plateau regime, the magnetization and spin current exhibit a slow decay to the steady state values described by the Liouvillian gap. We analytically establish its O(N^{-3}) O ( N − 3 ) scaling and also determine its coefficient.
We provide a rigorous construction of Markovian master equations for a wide class of quantum systems that encompass quadratic models of finite size, linearly coupled to an environment modeled by a set of independent thermal baths. Our theory can be applied for both fermionic and bosonic models in any number of physical dimensions and does not require any particular spatial symmetry of the global system. We show that, for nondegenerate systems under a full secular approximation, the effective Lindblad operators are the normal modes of the system, with coupling constants that explicitly depend on the transformation matrices that diagonalize the Hamiltonian. Both the dynamics and the steady-state (guaranteed to be unique) properties can be obtained with a polynomial amount of resources in the system size. We also address the particle and energy current flowing through the system in a minimal two-bath scheme and find that they hold the structure of Landauer's formula, being thermodynamically consistent.