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arXiv:2112.06959 · PRX Quantum

Volume-Law Entanglement Entropy of Typical Pure Quantum States

Eugenio Bianchi A, Lucas Hackl, Mario Kieburg, Marcos Rigol, Lev Vidmar

Published Jul 26, 2022• 0 citations
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Abstract

The behavior of the entanglement entropy of typical pure quantum states is pedagogically introduced, including recent conjectures on how it can be used as a diagnostic of quantum chaos and integrability.
DOI
10.1103/prxquantum.3.030201

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The entanglement entropy of subsystems of typical eigenstates of quantum many-body Hamiltonians has recently been conjectured to be a diagnostic of quantum chaos and integrability. In quantum chaotic systems it has been found to behave as in typical pure states, while in integrable systems it has been found to behave as in typical pure Gaussian states. In this tutorial, we provide a pedagogical introduction to known results about the entanglement entropy of subsystems of typical pure states and of typical pure Gaussian states. They both exhibit a leading term that scales with the volume of the subsystem, when smaller than one half of the volume of the system, but the prefactor of the volume law is fundamentally different. It is constant (and maximal) for typical pure states, and it depends on the ratio between the volume of the subsystem and of the entire system for typical pure Gaussian states. Since particle-number conservation plays an important role in many physical Hamiltonians, we discuss its effect on typical pure states and on typical pure Gaussian states. We prove that, while the behavior of the leading volume-law terms does not change qualitatively, the nature of the subleading terms can change. In particular, subleading corrections can appear that depend on the square root of the volume of the subsystem. We unveil the origin of those corrections. Finally, we discuss the connection between the entanglement entropy of typical pure states and analytical results obtained in the context of random matrix theory, as well as numerical results obtained for physical Hamiltonians.
In a seminal paper [Phys. Rev. Lett. 71, 1291 (1993)], Page conjectured that the entanglement entropy of typical pure states is Styp≃ln⁡DA−(1/2)DA2/DS_{\rm typ}\simeq\ln{\cal D}_{\rm A} - (1/2) {\cal D}_{\rm A}^2/{\cal D}Styp​≃lnDA​−(1/2)DA2​/D, where DA{\cal D}_{\rm A}DA​ and D{\cal D}D are the Hilbert space dimensions of the subsystem and the system, respectively, and typicality is with respect to the Haar measure. Typical pure states are hence (nearly) maximally entangled. We prove that S1+=ln⁡DA−[1/(2ln⁡2)](ln⁡DA)2/ln⁡DS^+_1=\ln{\cal D}_{\rm A} - [1/(2\ln2)] (\ln{\cal D}_{\rm A})^2/\ln{\cal D}S1+​=lnDA​−[1/(2ln2)](lnDA​)2/lnD is an upper bound for the average entanglement entropy of all many-body fermionic eigenstates of a class of translationally invariant quadratic Hamiltonians in one dimension, and that the variance vanishes with increasing system size. Consequently, whenever the size of the subsystem is not a vanishing fraction of the size of the system, typical eigenstates of such Hamiltonians have a volume-law entanglement but do not become maximally entangled as D→∞{\cal D}\rightarrow\inftyD→∞, i.e., they are qualitatively different from typical pure states. We also prove that, in the limit in which the subsystem size is a vanishing fraction of the system size, the average entanglement entropy is maximal.
A pure quantum state can fully describe thermal equilibrium as long as one focuses on local observables. The thermodynamic entropy can also be recovered as the entanglement entropy of small subsystems. When the size of the subsystem increases, however, quantum correlations break the correspondence and mandate a correction to this simple volume law. The elucidation of the size dependence of the entanglement entropy is thus essentially important in linking quantum physics with thermodynamics. Here we derive an analytic formula of the entanglement entropy for a class of pure states called cTPQ states representing equilibrium. We numerically find that our formula applies universally to any sufficiently scrambled pure state representing thermal equilibrium, i.e., energy eigenstates of non-integrable models and states after quantum quenches. Our formula is exploited as diagnostics for chaotic systems; it can distinguish integrable models from non-integrable models and many-body localization phases from chaotic phases.
Thermal equilibrium in quantum many-body systems can be fully described by pure quantum states as far as local observables are concerned, while the conventional description of it is based on mixed-state ensembles.The thermodynamic entropy, in that case, is identified with the entanglement entropy of small subsystems.It scales with the size of the subsystem, which is called the volume law of entanglement.When the size of the subsystem increases, however, the correspondence between thermal and entanglement entropies fails and there appears a quantum correction to the simple volume-law scaling.Explicating the scaling of the entanglement entropy with the subsystem size is hence of great importance in connecting quantum physics to thermodynamics as well as analyzing recent experiments on ultracold atoms.In this thesis, we study the volume law of entanglement for pure quantum states representing thermal equilibrium.We derive an analytic formula of the volume law of entanglement for a certain class of pure states called canonical Thermal Pure Quantum (cTPQ) states which represent thermal equilibrium.We illustrate an advantage of the formula by numerically calculating the entanglement entropy of the cTPQ states and applying the formula to it.Furthermore, we argue that our formula universally applies to any sufficiently scrambled pure state, even if the state is not thermal.We consider two examples of such scrambled states, namely, stationary pure states after quantum quench and energy eigenstates of general Hamiltonians with and without integrability.The entanglement entropy of the former states, including actual experimental data in ultracold atoms, is in an excellent agreement with our formula as long as the states are scrambled.For the latter states, we find that our formula works as a good fitting function in non-integrable models to extract information in the thermodynamic limit from finite size systems.We also show that our formula can distinguish eigenstates of integrable models from non-integrable ones.4.3.1 Review of result by Lu and Grover for eigenstates of non-integrable models . . . . . . . . . . . .
Many-body quantum eigenstates of generic Hamiltonians at finite-energy density typically satisfy the ``volume law'' of entanglement entropy: the von Neumann entanglement entropy and the Renyi entropies for a subregion scale in proportion to its volume. Here we provide a connection between the volume law and the sign structure of eigenstates. In particular, we ask the following question: Can a positive wave function support a volume law entanglement? Remarkably, we find that a typical random positive wave function exhibits a constant law for Renyi entanglement entropies Sn{S}_{n}Sn​ for n>1n>1n>1, despite arbitrary large-amplitude fluctuations. We also provide evidence that the modulus of the finite-energy density eigenstates of generic local Hamiltonians shows similar behavior.
We investigate the distribution of entanglement entropy in hybrid quantum circuits consisting of random unitary gates and local measurements applied at a finite rate. We demonstrate that higher moments of the entanglement entropy distribution, such as the ratio between the variance and the mean and the skewness, capture nontrivial features of the measurement-induced dynamics that are invisible to the mean entropy alone. We demonstrate that these quantities exhibit distinct and robust behaviors across the volume-law and area-law phases, and can serve as effective diagnostics of measurement-induced entanglement transitions. We propose a phenomenological model describing the effect of measurements in the area-law regime, which, when combined with the directed polymer in a random environment description of the volume-law phase, well matches numerical simulations across the entire phase diagram.