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Nonequilibrium Quantum Phase Transitions in the XY model: comparison of unitary time evolution and reduced density operator approaches

Shigeru Ajisaka, Felipe Barra

Published Aug 16, 2016• 28 citations
OpenAlex

Abstract

Abstract. We study nonequilibrium quantum phase transitions in XY spin 1/2 chain using the C ∗ algebra. We show that the well-known quantum phase transition at magnetic field h = 1 persists also in the nonequilibrium setting as long as one of the reservoirs is set to absolute zero temperature. In addition, we find nonequilibrium phase transitions associated to imaginary part of the correlation matrix for any two different temperatures of the reservoirs at h = 1 and h = hc ≡ |1 − γ2|, where γ is the anisotropy and h the magnetic field strength. In particular, two nonequilibrium quantum phase transitions coexist at h = 1. In addition we also study the quantum mutual information in all regimes and find a logarithmic correction of the area law in the nonequilibrium steady state independent of the system parameters. We use these nonequilibrium phase transitions to test the utility of two models of reduced density operator, namely Lindblad mesoreservoir and modified Redfield equation. We show that the nonequilibrium quantum phase transition at h = 1 related to the divergence of magnetic susceptibility is recovered in the mesoreservoir approach, whereas it is not recovered using the Redfield master equation formalism. However none of the reduced density operator approaches could recover all the transitions observed by the C ∗ algebra. We also study thermalization properties of the mesoreservoir approach.

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Reduced density matrix for nonequilibrium steady states: A modified Redfield solution approach

Juzar Thingna, Jian‐Sheng Wang, Peter Hänggi A

We describe a method to obtain the reduced density matrix (RDM) correct up to second order in system-bath coupling in nonequilibrium steady-state situations. The RDM is obtained via a scheme based on analytic continuation, using the time-local Redfield-like quantum master equation, which was earlier used by the same authors [J. Chem. Phys. 136, 194110 (2012)] to obtain the correct thermal equilibrium description. This nonequilibrium modified Redfield solution is then corroborated with the exact RDM obtained via the nonequilibrium Green's function technique for the quantum harmonic oscillator. Lastly, the scheme is compared to different quantum master equations (QMEs), namely the time-local Redfield-like and the Lindblad-like QMEs, in order to illustrate the differences between each of these approaches.

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Abstract. We study nonequilibrium quantum phase transitions in XY spin 1/2 chain using the C ∗ algebra. We show that the well-known quantum phase transition at magnetic field h = 1 persists also in the nonequilibrium setting as long as one of the reservoirs is set to absolute zero temperature. In addition, we find nonequilibrium phase transitions associated to imaginary part of the correlation matrix for any two different temperatures of the reservoirs at h = 1 and h = hc ≡ |1 − γ2|, where γ is the anisotropy and h the magnetic field strength. In particular, two nonequilibrium quantum phase transitions coexist at h = 1. In addition we also study the quantum mutual information in all regimes and find a logarithmic correction of the area law in the nonequilibrium steady state independent of the system parameters. We use these nonequilibrium phase transitions to test the utility of two models of reduced density operator, namely Lindblad mesoreservoir and modified Redfield equation. We show that the nonequilibrium quantum phase transition at h = 1 related to the divergence of magnetic susceptibility is recovered in the mesoreservoir approach, whereas it is not recovered using the Redfield master equation formalism. However none of the reduced density operator approaches could recover all the transitions observed by the C ∗ algebra. We also study thermalization properties of the mesoreservoir approach.
We study nonequilibrium quantum phase transitions in XY spin 1/2 chain using the C∗C^*C∗ algebra. We show that the well-known quantum phase transition at magnetic field h=1h = 1h=1 persists also in the nonequilibrium setting as long as one of the reservoirs is set to absolute zero temperature. In addition, we find nonequilibrium phase transitions associated to imaginary part of the correlation matrix for any two different temperatures of the reservoirs at h=1h = 1h=1 and h=hc≡∣1−γ2∣h = h_{\rm c} \equiv|1-γ^2|h=hc​≡∣1−γ2∣, where γγγ is the anisotropy and hhh the magnetic field strength. In particular, two nonequilibrium quantum phase transitions coexist at h=1h=1h=1. In addition we also study the quantum mutual information in all regimes and find a logarithmic correction of the area law in the nonequilibrium steady state independent of the system parameters. We use these nonequilibrium phase transitions to test the utility of two models of reduced density operator, namely Lindblad mesoreservoir and modified Redfield equation. We show that the nonequilibrium quantum phase transition at h=1h = 1h=1 related to the divergence of magnetic susceptibility is recovered in the mesoreservoir approach, whereas it is not recovered using the Redfield master equation formalism. However none of the reduced density operator approaches could recover all the transitions observed by the C∗C^*C∗ algebra. We also study thermalization properties of the mesoreservoir approach.
We obtain the steady-state phase diagram of a transverse-field XY spin chain coupled at its ends to magnetic reservoirs held at different magnetic potentials. In the long-time limit, the magnetization bias across the system generates a current-carrying nonequilibrium steady state. We characterize the different nonequilibrium phases as functions of the chain's parameters and magnetic potentials, in terms of their correlation functions and entanglement content. The mixed-order transition, previously observed for the case of a transverse-field Ising chain, is established to emerge as a generic feature of a wider class of out-of-equilibrium problems. The critical exponents associated with this universality class are determined analytically. Results are also contrasted with those obtained in the limit of Markovian reservoirs. Our findings should prove helpful in establishing the properties of nonequilibrium phases and phase transitions of extended open quantum systems.
We study a one-dimensional XX chain under nonequilibrium driving and local dephasing described by the Lindblad master equation. The analytical solution for the nonequilibrium steady state found for particular parameters in a previous study [M. Žnidarič J. Stat. Mech. (2010) L05002] is extended to arbitrary coupling constants, driving, and a homogeneous magnetic field. All one-, two-, and three-point correlation functions are explicitly evaluated. It is shown that the nonequilibrium stationary state is not Gaussian. Nevertheless, in the thermodynamic and weak-driving limit it is only weakly correlated and can be described by a matrix product operator ansatz with matrices of fixed dimension 4. A nonequilibrium phase transition at zero dephasing is also discussed. It is suggested that the scaling of the relaxation time with the system size can serve as a signature of a nonequilibrium phase transition.
Abstract Within the rigorous axiomatic framework for the description of quantum mechanical systems with a large number of degrees of freedom, we show that the nonequilibrium steady state, constructed in the quasifree fermionic system corresponding to the isotropic XY chain in which a finite sample, coupled to two thermal reservoirs at different temperatures, is exposed to a local external magnetic field, is breaking translation invariance and exhibits a strictly positive entropy production rate. Moreover, we prove that there exists a second-order nonequilibrium quantum phase transition with respect to the strength of the magnetic field as soon as the system is truly out of equilibrium.
In this Thesis we discussed several issues related to the dynamics of isolated quantum many-body systems. The brief overview of Chapter 1 highlighted a series of open fundamental theoretical questions which are crucial for the investigation of nonequilibrium phenomena. Among them, we mainly focused on the emergence of thermal behaviors and on the characterization of dynamical phase transitions and of the associated universal dynamics. To this end, we analyzed some paradigmatic models, such as the Fermi-Hubbard model, the quantum Ising chain, and the O(N) model. -Chapter 2: Absence of thermalization in a Fermi liquid. In this Chapter we report two results that question the common expectation of thermalization in a Landau-Fermi liquid after an interaction quench. We first consider the perturbative expansion in the interaction strength of the long-wavelength structure factor S(q) and show that it does not satisfy the hypothesis that steady-state averages correspond to thermal ones. In particular, S(q) has an analytical component ∼ const. + O(q^2) for q → 0, compatible with thermalization, but it retains also a nonanalytic term ∼ |q| characteristic of a Fermi liquid at zero-temperature. In real space, this nonanalyticity turns in a power-law decay of the density-density correlations, in contrast with the exponential decay associated to thermalization. We next analyze the low-density case, where one can obtain results valid at any order in interaction but at leading in the density, and find that in the steady state the momentum distribution jump at the Fermi surface is strictly finite, though smaller than at equilibrium. -Chapter 3: Nonadiabatic stationary behavior in a driven Ising chain. In this Chapter we discuss the emergence of a nonadiabatic behavior in the dynamics of the order parameter in a low-dimensional system subject to a linear ramp of one of its parameters within a gapped phase, which should be the most favorable situation for an adiabatic evolution. We study in details the dynamics of the spontaneous magnetization m_x(t) in a quantum Ising chain after a linear variation in time of the transverse field within the ordered phase. In particular, focusing on the value of the order parameter at the end of the ramp m_x(τ), we show that the smaller the switching rate of the transverse field is the closer m_x(τ) gets to its ground state value. Nonetheless, this apparently small correction to adiabaticity eventually leads to the disruption of the order exponentially fast in the subsequent time evolution, no matter how slowly the ramp is performed. -Chapter 4: Aging and coarsening in isolated quantum systems after a quench. This Chapter analyzes the nonequilibrium dynamics of an isolated quantum system after a sudden quench to the dynamical critical point, where the emergence of scaling and universal exponents is expected, due to the absence of time and length scales. We explore these features for a bosonic interacting scalar field theory with O(N) symmetry in the large-N limit, where the model is exactly solvable and the exponents and scaling forms of the relevant two-time correlation functions can be analytically calculated. Moreover, we provide evidence of the emergence of a dynamical scaling behavior also for quenches below the dynamical critical point, associated with coarsening. We find that the latter case is characterized by the same scaling functions as those describing the critical case, yet with different exponents. -Chapter 5: Dynamical transitions and statistics of excitations. In this Chapter we study the dynamics of the O(N) model (introduced in the previous Chapter) resulting from a different protocol: a linear ramp of one of its parameters. We find that the presence of a dynamical phase transition, as well as its critical properties, are robust against the change of the protocol. We show that a characterization based on the critical dimensions and exponents would suggest that the dynamical phase transition is analogous to the equilibrium thermal one. However, its nonequilibrium nature becomes evident analyzing the statistics of excitations produced in the ramp process. In particular, the critical properties are encoded in the fluctuations in the number of excitations, which display qualitatively different behaviors depending on the ramp being performed above, at, or below the dynamical critical point. These behaviors bear no dependence on the duration of the protocol.
We describe a method to obtain the reduced density matrix (RDM) correct up to second order in system-bath coupling in nonequilibrium steady-state situations. The RDM is obtained via a scheme based on analytic continuation, using the time-local Redfield-like quantum master equation, which was earlier used by the same authors [J. Chem. Phys. 136, 194110 (2012)] to obtain the correct thermal equilibrium description. This nonequilibrium modified Redfield solution is then corroborated with the exact RDM obtained via the nonequilibrium Green's function technique for the quantum harmonic oscillator. Lastly, the scheme is compared to different quantum master equations (QMEs), namely the time-local Redfield-like and the Lindblad-like QMEs, in order to illustrate the differences between each of these approaches.