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arXiv:1505.07811

How fast do stabilizer Hamiltonians thermalize?

Kristan Temme, Michael J. Kastoryano

Published May 28, 2015• 5 citations
arXivHTMLPDF

Abstract

We present rigorous bounds on the thermalization time of the family of quantum mechanical spin systems known as stabilizer Hamiltonians. The thermalizing dynamics are modeled by a Davies master equation that arises from a weak local coupling of the system to a large thermal bath. Two temperature regimes are considered. First we clarify how in the low temperature regime, the thermalization time is governed by a generalization of the energy barrier between orthogonal ground states. When no energy barrier is present the Hamiltonian thermalizes in a time that is at most quadratic in the system size. Secondly, we show that above a universal critical temperature, every stabilizer Hamiltonian relaxes to its unique thermal state in a time which scales at most linearly in the size of the system. We provide an explicit lower bound on the critical temperature. Finally, we discuss the implications of these result for the problem of self-correcting quantum memories with stabilizer Hamiltonians.

DOI
10.48550/arxiv.1505.07811

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We present rigorous bounds on the thermalization time of the family of quantum mechanical spin systems known as stabilizer Hamiltonians. The thermalizing dynamics are modeled by a Davies master equation that arises from a weak local coupling of the system to a large thermal bath. Two temperature regimes are considered. First we clarify how in the low temperature regime, the thermalization time is governed by a generalization of the energy barrier between orthogonal ground states. When no energy barrier is present the Hamiltonian thermalizes in a time that is at most quadratic in the system size. Secondly, we show that above a universal critical temperature, every stabilizer Hamiltonian relaxes to its unique thermal state in a time which scales at most linearly in the size of the system. We provide an explicit lower bound on the critical temperature. Finally, we discuss the implications of these result for the problem of self-correcting quantum memories with stabilizer Hamiltonians.
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We prove that spin chains weakly coupled to a large heat bath thermalize rapidly at any temperature for finite-range, translation-invariant commuting Hamiltonians, reaching equilibrium in a time which scales logarithmically with the system size. This generalizes to the quantum regime a seminal result of Holley and Stroock from 1989 for classical spin chains and represents an exponential improvement over previous bounds based on the nonclosure of the spectral gap. We discuss the implications in the context of dissipative phase transitions and in the study of symmetry protected topological phases.
Many physical phenomena, including thermalization in open quantum systems and quantum Gibbs sampling, are modeled by Lindbladians approximating a system weakly coupled to a bath. Understanding the convergence speed of these Lindbladians to their steady states is crucial for bounding algorithmic runtimes and thermalization timescales. We study two such families of processes: one characterizing a repeated-interaction Gibbs sampling algorithm, and another modeling open many-body quantum thermalization. We prove that both converge in polynomial time for several non-commuting systems, including high-temperature local lattices, weakly interacting fermions, and 1D spin chains. These results demonstrate that simple dissipative quantum algorithms can prepare complex Gibbs states and that Lindblad dynamics accurately capture thermal relaxation. Our proofs rely on a novel technical result that extrapolates spectral gap lower bounds from quasi-local Lindbladians to the non-local generators governing these dynamics.
We discuss several thermodynamic criteria that have been introduced to characterize the thermal stability of a self-correcting quantum memory. We first examine the use of symmetry-breaking fields in analyzing the properties of self-correcting quantum memories in the thermodynamic limit; we show that the thermal expectation values of all logical operators vanish for any stabilizer and any subsystem code in any spatial dimension. On the positive side, we generalize the results of Alicki et al to obtain a general upper bound on the relaxation rate of a quantum memory at nonzero temperature, assuming that the quantum memory interacts via a Markovian master equation with a thermal bath. This upper bound is applicable to quantum memories based on either stabilizer or subsystem codes.
We study the scaling behavior of the relaxation dynamics to thermal equilibrium when a quantum system is near the quantum critical point. In particular, we investigate systems whose relaxation dynamics is described by a Lindblad master equation. We find that the universal scaling behavior not only appears in the equilibrium stage at the long-time limit but also manifests in the nonequilibrium relaxation process. While the critical behavior is dictated by the low-lying energy levels of the Hamiltonian, the dissipative part in the Lindblad equation also plays important roles in two aspects: First, the dissipative part makes the high-energy levels decay fast, after which the universal behavior controlled by the low-lying modes emerges. Second, the dissipation rate gives rise to a time scale that affects the scaling behavior. We confirm our theory by solving the Lindblad equation for the one-dimensional transverse-field Ising model.
For sufficiently low reservoir temperatures, it is known that open quantum systems subject to decoherent interactions with the reservoir relax toward their ground state in the weak coupling limit. Within the framework of quantum master equations, this is formalized by the Born-Markov-secular (BMS) approximation, where one obtains the system Gibbs state with the reservoir temperature as a stationary state. When the solution to some problem is encoded in the (isolated) ground state of a system Hamiltonian, decoherence can therefore be exploited for computation. The computational complexity is then given by the scaling of the relaxation time with the system size nnn. We study the relaxation behavior for local and nonlocal Hamiltonians that are coupled dissipatively with local and nonlocal operators to a bosonic bath in thermal equilibrium. We find that relaxation is generally more efficient when coherences of the density matrix in the system energy eigenbasis are taken into account. In addition, the relaxation speed strongly depends on the matrix elements of the coupling operators between initial state and ground state. We show that Dicke superradiance is a special case of our relaxation models and can thus be understood as a coherence-assisted relaxation speedup.