Fluctuation-dissipation relations and critical quenches in the transverse field Ising chain

Fluctuation-dissipation relations and
critical quenches in the transverse field Ising chain

Laura Foini SISSA – International School for Advanced Studies and INFN, via Bonomea 265, 34136 Trieste, Italia Laboratoire de Physique Théorique, Ecole Normale Supérieure de Paris, UMR 8549, 24 rue Lhomond 75234 Paris Cedex 05, France    Leticia F. Cugliandolo Université Pierre et Marie Curie – Paris VI, Laboratoire de Physique Théorique et Hautes Energies, UMR 7589, Tour 15 5ème étage, 4 Place Jussieu, 75252 Paris Cedex 05, France    Andrea Gambassi SISSA – International School for Advanced Studies and INFN, via Bonomea 265, 34136 Trieste, Italia Université Pierre et Marie Curie – Paris VI, Laboratoire de Physique Théorique et Hautes Energies, UMR 7589, Tour 15 5ème étage, 4 Place Jussieu, 75252 Paris Cedex 05, France
July 17, 2019
Abstract

Dynamic correlation and response functions of classical and quantum systems in thermal equilibrium are connected by fluctuation-dissipation theorems, which allow an alternative definition of their (unique) temperature. Motivated by this fundamental property, we revisit the issue of thermalization of closed many-body quantum systems long after a sudden quench, focussing on the non-equilibrium dynamics of the Ising chain in a critical transverse field. We show the emergence of distinct observable-dependent effective temperatures, which rule out Gibbs thermalization in a strict sense but might still have a thermodynamic meaning.

Introduction. The development of experimental techniques which prevent dissipation in quantum many-body systems has triggered increasing interest in the non-equilibrium dynamics of such closed systems. The unitary non-equilibrium dynamics of a system initially prepared in a state which is not an eigenstate of its Hamiltonian is called a quantum quench. Basic questions as to whether a stationary state is reached and how this can be characterized naturally arise. These questions have been addressed in a number of simple models, including the one-dimensional systems reviewed in Refs. Karevski (); reviews-chains (). Early studies led to the following picture: Non-integrable systems should eventually reach a thermal stationary state characterized by a Gibbs distribution with a single temperature. Integrable systems, instead, are not expected to thermalize but their asymptotic stationary state should nonetheless be described by a so-called generalized Gibbs ensemble (GGE) with one effective temperature for each conserved quantity Rigol (); GGE_other_models (); GGE_Ising (); Calabrese11 (). Interestingly enough, depending on the specific quantity and the system’s parameters a Gibbs ensemble turns out to capture anyhow some relevant features of the non-equilibrium dynamics of integrable systems Rossini10 (). In particular, observables that are non-local in the quasi-particles display numerically the same relaxation scales as in equilibrium with a suitable effective temperature, at least for small quenches Rossini10 (); Calabrese11 (). Local quantities instead do not, with possible exceptions for quenches at criticality.

Our purpose is to revisit the debated issue of thermalization in closed quantum systems with tools developed for the study of classical and quantum dissipative glassy systems. The analysis of thermalization in closed quantum systems focused so far on the property that expectation values of quantities — such as (i) the conserved energy and two-point correlation functions depending on either (ii) one or (iii) two times — should behave, at long times, as the corresponding averages calculated on suitable statistical ensembles. However, an equally important property of thermal equilibrium states of both classical and quantum systems is the validity of model-independent fluctuation-dissipation theorems (FDTs) Kubo (), which relate linear response and correlation functions independently of their functional form. Focusing on two-time quantities, we investigate thermalization issues from this perspective.

Before getting into the technical details, let us explain why fluctuation-dissipation relations (FDRs) should be more relevant to thermalization issues than the precise functional decay of observables. Take phase separating systems as an example. The expectation values of one-time quantities – such as the energy density (i) or observables of the type (ii) – reach equilibrium values, suggesting the equilibration of the sample at the bath temperature. This is, however, incorrect as proven by the fact that observables of type (iii), such as delayed density correlations and linear responses, decay in more than one dynamic scale, and in the slowest they do algebraically, as opposed to the typical exponential equilibrium relaxation. In spite of this, one can still define a bona fide effective temperature from FDRs that link correlations to their associated linear response Cugliandolo97 () as long as one distinguishes different pairs of observables and the time-scales in which they evolve. Indeed, some observables basically ignore others — they do not interact — equilibrate quickly with the environment and are characterized by its temperature. This is the case of particle velocities. Positions, instead, do not equilibrate with the bath but acquire the same effective temperature, i.e., they partially equilibrate, in their own common regime of relaxation. This notion applies to many other systems with slow dynamics and constitutes the basis of, e.g., a consistent thermodynamic picture of non-equilibrium glassy dynamics as realized in mean-field theory Teff-reviews (). A quantum finite-dimensional example with effective temperatures are electronic tight-binding dissipative one-dimensional models driven by external fields Caso ().

We explore up to which extent these ideas carry over to the non-equilibrium dynamics of a highly excited closed quantum system. For concreteness, we focus on critical quenches in which the system’s parameters for times are tuned to be at an equilibrium (quantum) critical point. The detailed analysis of the effective temperature based on FDRs in classical thermal quenches Teff-reviews (); Teff-critical () demonstrated that such a parameter has a thermodynamic meaning for very late epochs only Godreche (), when one of the involved times is much longer than the other (see, however, Ref. Andrea ()).

The model. To illustrate our approach, we focus on the simplest quantum integrable interacting model, the transverse field Ising chain reviews-chains ()

(1)

with periodic boundary conditions and even . The Pauli matrices satisfy the SU(2) algebra on the same site and commute on different sites. In what follows we set and we measure time in units of and the temperature in units of . The model is exactly solved by a Jordan-Wigner transformation to free fermions followed by a Bogoliubov rotation in momentum space mccoy (). The energy of the elementary fermionic excitations with momentum is . For and a quantum critical point at separates a paramagnetic phase (PM, ) with , from a ferromagnetic phase (FM, ) with spontaneous symmetry breaking and long-range order along the direction. for all .

The system is prepared at in the ground state of , while it subsequently evolves with , i.e., at the critical point. The quench from to injects an extensive amount of energy into the system which is henceforth conserved. After a transient (studied in Refs. Igloi00 (); Igloi11 () for the chain with free boundaries) the system reaches an asymptotic stationary regime. A crucial quantity in the description of the dynamics is the difference between the Bogoliubov angles diagonalizing and :

(2)

encodes the dependence on the initial state and fixes the non-thermal statistics of the excitations created at .

A criterion that has been used to define an effective temperature is to require that the energy after the quench — quantity (i) in the Introduction — equals the average over a thermal equilibrium ensemble reviews-chains (); Rossini10 (). For model (1) this implies Rossini10 ()

(3)

which results in the shown in Figs. 1 and 3 with a dashed black line. Requiring, instead, the integrand in Eq. (3) to vanish defines the mode-dependent of the GGE Calabrese11 (); GGE_Ising ().

FDT. We focus on the symmetrized and anti-symmetrized two-time correlations of two operators and in the Heisenberg representation, ,

(4)

where . More precisely, we consider connected correlations that we still denote by . While approaches the classical correlation function for , is related to the linear response function through the Kubo formula  Kubo () which is valid in and out of equilibrium [ and ]. The asymptotic stationary regime is formally defined by the limit . When it is physically established depends on the observable and . Natural choices for and are the order parameter and the transverse magnetization . The autocorrelation functions, , are non-local with respect to the quasi-particles while those of , , are local in the same variables reviews-chains ().

In Gibbs equilibrium at inverse temperature the FDT connects and , via the model-independent time-domain and frequency-domain relations Kubo ()

(5)
(6)

respectively. We reinstated to make the classical limit, , transparent. The FDR definition of an effective temperature amounts to replacing by in Eqs. (5) and (6) [with a -dependence in non-stationary (glassy) cases], i.e.,

(7)

This is the definition that we shall repeatedly use below.

Before presenting our results let us summarize what is known about for . In equilibrium () decays algebraically as at and as at finite  Rossini10 (). Out of equilibrium the decay of is  Igloi00 (). For the special case of a fully polarized initial condition ) follows the same decay, as can be inferred from the results in Ref. Karevski (). Instead, a generic exponential relaxation of was argued in Calabrese06 () using semi-classical methods and later shown to hold exactly Calabrese11 (). This is in contrast to the power-law decay of the equilibrium order-parameter spatio-temporal correlations. As far as we know, has not been analyzed so far. Here we complete this picture by calculating and for generic . We also study , where .

The transverse local magnetization. For we found that and decay as a sum of power laws of and . Thus, no characteristic time can be identified and, in addition, one cannot compare these functions to the thermal ones in order to define an effective temperature, as done in Refs. Rossini10 (); Igloi11 (); Calabrese11 () for other observables [type (iii) of the Introduction]. Taking one finds the stationary relaxation

(8)
(9)

with . The complementary analysis in the frequency domain allows us to define a frequency-dependent via the FDR in Eq. (7). The function is shown in Fig. 1 for as a (red) solid line and it has to be compared with the constant value obtained from Eq. (3), as in Ref. Rossini10 (), shown as a black dashed line. The asymptotic regime corresponds to the limit , zoomed in the inset, in which diverges logarithmically with the law (green dashed line). We conclude that, although takes a thermal value Rossini10 (), the dynamics of is not compatible with an equilibrium thermal behavior. For other values of , still vanishes at and but it is not concave for  laura-prep (). For increasingly narrower quenches with , uniformly over all frequencies.

The transverse global magnetization. The long-time stationary decay of the global magnetization correlations are even slower than the one of notaM ():

(10)
(11)

The leading-order decay is the same as in equilibrium at finite . However, while the prefactor depends upon in equilibrium Niemeijer (), out of equilibrium the dependence on appears only at the next-to-leading order, i.e., the long- limit of does not retain memory of the initial condition.

The (blue) dash-dotted line in Fig. 1 is as obtained from the FDR (7), applied to . approaches at low frequencies, it vanishes for and becomes non-monotonic for , developing a shallow local maximum. Naively, one may expect to recover this value by treating the time-domain FDR in the long- limit as follows. Replacing by a constant effective value in the rhs of Eq. (5), the integral can be written as series of odd time derivatives of . Inserting Eqs. (10) and (11) in the rhs and lhs of this expression, respectively, yields for and therefore . The fact that indicates that cannot be approximated by an average constant in the integral. Indeed, since only the derivatives of the oscillating factor in (10) contribute to the leading order of Eq. (5), is the one of the oscillatory frequency, which coincides with the threshold value and, for , diverges as . Such threshold results from the maximum of the dispersion relation and the quadratic dependence of on the fermionic excitations. It is therefore unclear whether can be recovered from the FDR in the time domain.

Interestingly enough, it turns out laura-prep () that each frequency selects a mode such that and defined here from the FDR (7) coincides with the temperature of the GGE.

Figure 1: (Color online.) Comparison between the effective temperature defined via the frequency-domain FDR applied to (red solid line) and (blue dash-dotted line), and the energy definition (black dashed horizontal line) for . The inset highlights the logarithmic divergence of for .

The order parameter. Equations (8), (9), (10) and (11) are invariant under because [see Eq. (2)] is the sole quantity bringing about the dependence on in the stationary limit of laura-prep (). In the same limit and for we find numerically that this invariance also holds for . Henceforth we restrict to quenches originating from the FM phase. We computed for a chain with and with the methods employed in Refs. mccoy (); Rossini10 (); Igloi00 (). Our numerical results are fitted very accurately by

(12)
(13)

with (numerically) the same rate as the one analytically proved Calabrese11 () to characterize the exponential long-time decay of . The expression for finds further support from the fact that with the substitution one recovers the equilibrium  Deift (); nota () in this as well as other statistical averages. Although several fitting parameters are involved in Eqs. (12) and (13), we tested these expressions in various instances and they turned out to be always remarkably accurate already for  laura-prep (). In Fig. 2 we show and for , together with a zoom into the long-time decay and its comparison with the leading exponential decay in the upper inset. The lower inset confirms the high quality of the fit of the correction terms to the forms given in Eqs. (12) and (13) which are actually indistinguishable from the data. The non-equilibrium coherence time decreases upon increasing , i.e., the energy injected into the system and for . While the parameters depend on , their ratio does not within our numerical accuracy. More details on the fitting parameters of the oscillating (lattice) correction will be presented in Ref. laura-prep ().

Figure 2: (Color online.) Decay of the order-parameter correlation (blue line) and the linear response (red line) for . Upper inset: zoom into the long- decay that demonstrates the exponential relaxation with the characteristic time defined in the text (dashed green line). Lower inset: and vs. ; the green dashed line is the envelope of the damped oscillations, in agreement with Eqs. (12) and (13).

The effective temperatures determined in the frequency and in the time domain are equivalent in this case. As discussed above, replacing by a constant , turns the rhs of the FDT (5) in the time domain into a series of time derivatives of which yields

(14)

for , i.e., neglecting the oscillatory corrections in Eqs. (12) and (13). Alternatively, Eq. (7) yields for which numerically coincides with the constant value in Eq. (14). For one recovers the classical limit . All three determinations of are shown in Fig. 3 as functions of and they are compared to (dashed line) from Eq. (3Rossini10 ().

Figure 3: (Color online.) dependence of the order parameter effective temperature compared to defined from the energy [see Eq. (3)] (dashed line). The solid lines, from bottom to top, indicate the values determined on the basis of the classical limit of the FDR in the time domain, of the limit of the frequency-domain FDR, of Eq. (14), and of the limit of the frequency-domain FDR but for spins separated by a distance . The dependence on can be read from the one of and Eq. (14).

We completed our analysis by studying space-dependent correlations and we found that they yield analogous results, as shown in Fig. 3 for the -component of two spins at distance . (Note that differently from case shown in Fig. 2, correlations with display a light-cone effect due to the finite speed of the quasi-particles Calabrese06 (); Calabrese11 (); Igloi11 (); laura-prep ().)

Conclusions. Independently of the functional form of the correlations involved, the FDRs allow us to define various effective temperatures. We calculated the (self) FDR for three observables that are local () or non-local () in space and local (, ) or non-local () in the quasi-particles. is not compatible with Gibbs thermal equilibrium at any effective temperature. The frequency-domain FDR for yields a finite in the limit . Frequency and time-domain determinations of are equivalent. and have the same qualitative dependence on but they differ (also from ). This excludes a single temperature effective Gibbs description (as the one discussed in Ref. Mitra11 ()) of the full stationary dynamics of this model but the question remains as to whether some of the temperatures which emerge can be attributed a thermodynamic meaning.

We finally stress that a bona fide thermal behavior should be accompanied by the validity of suitable FDTs also in the context of quantum quenches.

Acknowledgments. We thank F. Iglói, G. Santoro, G. Semerjian, A. Silva, F. Zamponi for discussions. A. Gambassi and L. F. Cugliandolo thank LPTHE and ICTP, respectively, for hospitality during the preparation of this work that was financially supported by ANR-BLAN-0346 (FAMOUS) and CNRS.

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