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. 2024 Mar 3;26(3):229. doi: 10.3390/e26030229

Quadratic Growth of Out-of-Time-Ordered Correlators in Quantum Kicked Rotor Model

Guanling Li 1, Wenlei Zhao 1,*
Editor: Stefano Mancini1
PMCID: PMC10969592  PMID: 38539742

Abstract

We investigate both theoretically and numerically the dynamics of out-of-time-ordered correlators (OTOCs) in quantum resonance conditions for a kicked rotor model. We employ various operators to construct OTOCs in order to thoroughly quantify their commutation relation at different times, therefore unveiling the process of quantum scrambling. With the help of quantum resonance condition, we have deduced the exact expressions of quantum states during both forward evolution and time reversal, which enables us to establish the laws governing OTOCs’ time dependence. We find interestingly that the OTOCs of different types increase in a quadratic function of time, breaking the freezing of quantum scrambling induced by the dynamical localization under non-resonance condition. The underlying mechanism is discovered, and the possible applications in quantum entanglement are discussed.

Keywords: quantum scrambling, quantum chaos, kicked rotor

1. Introduction

Quantum scrambling, a fundamental concept elucidating the spread of information across multiple degrees of freedom that is inaccessible via local measurements, has garnered extensive attention in quantum information [1,2,3,4], quantum chaos [5,6,7,8,9], and condensed matter physics [10,11,12,13]. It is well known that the out-of-time ordered correlators (OTOCs) can quantify the process of information scrambling with relevance to the operator growth [14,15]. The exponential growth of OTOCs, facilitated by exponential instability of chaos, produces the boundary of the light cone of information scrambling in many-body systems [16,17], for which the butterfly velocity of scrambling is closely related to the quantum Lyapunov exponent [18,19,20]. The relaxation of OTOCs can detect the character of both the quantum thermalization and quantum entanglement in many-body systems [21,22], providing insights into the underlying connection between quantum chaos and information scrambling [23,24,25]. The dynamics of OTOCs can be used as an order parameter to diagnose phase transitions in both Hermitian [26] and non-Hermitian chaotic systems [27]. Interestingly, genuine quantum chaos, specifically the superexponential instability induced by delta-kicking modulation in nonlinear interactions, can cause the superexponential growth of OTOCs [28], representing a new phenomenon of information scrambling [29,30].

The variants of the quantum kicked rotor (QKR) model under resonance conditions serve as ideal platforms to explore fascinating physics of quantum coherence [31], which has significant implications for the fundamental aspects of quantum transport [32,33] and topological new phases in Floquet systems [34,35,36,37]. The existence of the flat band of quasi-energy spectrum determines the exponential diffusion dynamics in the on-resonance double-kicked rotor model [38]. The resonance condition yields Floquet spectrum [39,40,41] analogous to Hofstadter’s butterfly of an integrable system [42,43,44] and topological phase transitions reminiscent of the integer quantum Hall effect [45,46]. Moreover, a dynamical analog of the integer quantum Hall effect emerges from an intrinsic chaos in spin-1/2 QKR model, enriching our understanding of the quantum topological phenomena induced by chaos [47,48]. Interestingly, the spinor QKR model with quantum resonance condition provides a versatile playground to realize the quantum walk in momentum space [49,50], proposing a new protocol for the manipulation of the quantum transport with Floquet engineering [51]. The state-of-the-art experiments in atom-optics have indeed realized the QKR model and verified the dynamical phase transition and quantum walk therein by precisely tailoring the resonance condition for the driven period [52]. This paves the way for engineering exotic behavior of quantum information [53] and energy diffusion [54] in various generalization of the QKR model.

In this context, we investigate both analytically and numerically the dynamics of different types of OTOCs under the quantum resonance condition. The first type OTOCs Cp involves two angular momentum operators. Furthermore, the second one CT is constructed by the combination of the translation operator and angular momentum operator. We have derived the exact expression of the quantum state during both forward evolution and time reversal under quantum resonance conditions, which enables us to precisely establish the law governing the time dependence of OTOCs. Our findings reveal that both Cp and CT exhibit unbounded quadratic growth, indicating a power law scrambling behavior in their long-term evolutions. The observation of similar time dependence laws for different OTOCs suggests a universality in this power law growth for the QKR model. It is known that the exotic physics exhibited by the QKR model under quantum resonance conditions, such as ballistic energy diffusion and topologically protected transport in momentum space, originates from the essential quantum coherence effects, without classical counterparts. Our findings unveil the role of quantum coherence in facilitating quantum scrambling, a connection of potential significance for applications in quantum information.

The paper is organized as follows. In Section 2, we describe the system and show the quadratic growth of OTOCs. In Section 3, we show our theoretical analysis. A summary is presented in Section 4.

2. Model and Main Results

The dimensionless Hamiltonian of the QKR model reads

H=p22+Kcos(θ)nδ(ttn), (1)

where p=ieff/θ is the angular momentum operator, θ is the angle coordinate, with commutation relation [θ,p]=ieff. Here, eff denotes the effective planck’s constant, and K is the kicking strength [55]. One experimental realization of the QKR model involves ultracold atoms exposed to a pulsed laser standing field that mimics a delta-kicking potential [56]. The eigenequation of the angular momentum operator is p|φn=pn|φn with an eigenvalue of pn=neff and eigenstate of θ|φn=einθ/2π. With the complete basis of |φn, an arbitrary state can be expanded as |ψ=nψn|φn. One period evolution of the quantum state from tn to tn+1 is governed by |ψ(tn+1)=U|ψ(tn). The Floquet operator U involves two components, i.e., U=UfUK, where the Uf=expip2/2eff represents the free evolution operator and the kicking term is denoted by UK=expiKcos(θ)/eff.

The OTOCs are defined using the average of the squared commutator, i.e., C(t)=[A(t),B]2. Here, both A(t)=U(t)AU(t) and B are evaluated in the Heisenberg picture. The average · refers to the operator’s expectation value concerning the initial state ψ(t0)|·|ψ(t0) [29,57,58,59,60]. We investigate two distinct OTOCs, one denoted as Cp=[p(t),p]2, and the other as CT=[Tt,p]2, where T=expiϵp/eff represents the translation operator. We focus solely on the quantum resonance condition, i.e., eff=4π. Without loss of generality, we choose an initial state ψ(θ,t0)=cos(θ)/π. Our main findings can be summarized by the following relationships

Cp(t)=12π2K2t2, (2)

and

CT(t)=sin2ϵ22+cos(ϵ)K2t2. (3)

These relations clearly demonstrate the existence of the quadratic growth of different OTOCs.

In order to confirm our above theoretical predictions, we numerically calculate both the Cp and CT for different Ks. Our results demonstrate that for a specific K (e.g., K=1 in Figure 1), both Cp and CT increase unboundedly with time. Furthermore, the larger the K, the faster they increase, following perfectly with the relations described in Equations (2) and (3). The continuous, unsaturated growth of OTOCs is attributed to the delocalization mechanism under quantum resonance conditions. When the delocalization mechanism is absent, the process of dynamical localization in quantum non-resonance conditions leads to the saturation of OTOCs, which has been reported in our previous investigation in Ref. [27]. It is noteworthy that the dependency of CT on the parameter ϵ offers a means of manipulating quantum scrambling by adjusting the translation operator, shedding light on the quantum control of non-Hermitian Floquet systems.

Figure 1.

Figure 1

Time dependence of the Cp (a) and CT (b) for K=1 (squares), 2 (diamonds), 3 (circles), and 5 (triangles). Red lines in (a,b) indicate our theoretical prediction in Equations (2) and (3), respectively. In (b), the value of the translation parameter is ϵ=π.

The quadratic growth in OTOCs also emerges when we use the translation operator T=exp(iϵp/eff) and a projection operator onto an initial state B=|ψ(t0)ψ(t0)| for OTOCs. In this situation, one can obtain the relation C(t)=1FO, with FO=|ψ(t0)|T|ψ(t0)|2 being named as fidelity out-of-time-ordered correlators (FOTOCs). Under the condition ϵ/eff1, straightforward derivation yields the approximation C(t)(ϵ/eff)2p2(t)p(t)2, by neglecting the terms in the Taylor expansion of T=exp(iϵp/) of orders larger than two. The mean momentum is zero, i.e., p(t)=0 due to the symmetry of both the specific initial state ψ(θ,t0)=cos(θ)/π and the kicking potential. Therefore, the OTOCs is proportional to the mean energy, i.e., C(t)(ϵ/eff)2p2(t)(ϵKt/2eff)2, indicating clearly the quadratic growth. Note that the Fourier spectrum of the FOTOCs FO can be utilized in constructing the Rényi entropy [61,62,63]. In fact, FOTOCs have been used to characterize the multiple entanglements among different degrees of freedom in the kicked top model, which can be regarded as a collective of many spins [64]. It is known that the QKR model is a limit of the kicked top model with angular momentum being infinity [65]. This provides the theoretical foundation for the significant implications of the quadratic growth of OTOCs in measuring the buildup of quantum entanglement.

In the atom-optics realization of the QKR model, the experimental constraints in practice often introduce very small detuning from the exact quantum resonance condition [66]. We further consider the effects of the slight variation in the value of eff from quantum resonance condition, i.e., eff=4π+Δ on the quantum scrambling. In this situation, there is a fictitious classical limit in which the parameter Δ plays the role of the effective Planck’s constant [66,67]. We should note that traditional definition of the semiclassical limit with eff tending to zero does not make sense for the resonance case as eff=4π. Our numerical results show that for a specific Δ (e.g., Δ=0.0025 in Figure 2a), the Cp follows the quadratic growth of Δ=0 for finite time duration, i.e., t<tc, after which it fluctuates around a saturation level. Interestingly, the saturate level decreases with the increase in Δ. For sufficiently large Δ (e.g., Δ=0.1), the Cp remains almost at its initial value and does not increases with time. We further investigate the Cp at a specific time for different Δ. The inset in Figure 2a shows that the Cp(t=500) decreases with some fluctuations as the absolute value of Δ departs from zero, which demonstrates the suppression of OTOCs by the variation of eff from quantum resonance condition. The time evolution of CT also exhibits the reduction from the quadratic growth in Δ=0 with the increase in Δ (see Figure 2b). When the |Δ| increases from zero, the QKR transitions to the quantum non-resonance regime, where the mechanism of dynamical localization suppresses the growth of OTOCs [27].

Figure 2.

Figure 2

Time dependence of the Cp (a) and CT (b) for K=1. In (a), Δ=0 (squares), 0.0025 (circles), 0.005 (triangles), and 0.1 (diamonds). Inset: The Cp at time t=500 versus Δ. In (b), Δ=0 (squares), 5×105 (circles), 1×104 (triangles), and 0.1 (diamonds). Inset: The CT at time t=500 versus Δ. Red lines in (a,b) indicate our theoretical prediction in Equations (2) and (3), respectively. In (b), the value of the translation parameter is ϵ=π.

3. Theoretical Analysis

It is straightforward to derive the relation

C(t)=C1(t)+C2(t)2ReC3(t), (4)

where the first two terms on the right side, i.e., two-points correlator, are defined as

C1(t):=A(t)B2A(t)=ψR(t0)|B2|ψR(t0), (5)
C2(t):=BA(t)A(t)B=φR(t0)|φR(t0), (6)

and the four-point correlator is given by

C3(t):=A(t)BA(t)B=ψR(t0)|B|φR(t0), (7)

with |ψR(t0)=U(t)AU(t)|ψ(t0) and |φR(t0)=U(t)AU(t)B|ψ(t0). Here, Re denotes the real part of the complex variable [29].

The derivation of C1 at a specific time t=tn involves three sequential steps [68]. Firstly, evolving the initial state |ψ(t0) from t0 to tn yields |ψ(tn)=U(tn,t0)|ψ(t0). Secondly, applying operator A to |ψ(tn) produces |ψ˜(tn)=A|ψ(tn). Finally, the time reversal from tn to t0 for |ψ˜(tn) results in |ψR(t0)=U(tn,t0)|ψ˜(tn). Equation (5) indicates that C1 is the expectation value of operator B2 for |ψR(t0). The process to derive C2 at time t=tn involves four steps. Firstly, applying the operator B to the initial state |ψ(t0) yields the state |φ(t0)=B|ψ(t0). Secondly, the forward evolution for the state |φ(t0) results in a state |φ(tn)=U(tn,t0)|φ(t0). In the third step, we apply the operator A to the state |φ(tn), which creates a new state |φ˜(tn)=A|φ(tn). The fourth step involves a time reversal for the state |φ˜(tn), giving |φR(t0)=U(tn,t0)|φ˜(tn). The norm of |φR(t0) defines C2 as shown in Equation (6). With the two states |ψR(t0) and |φR(t0), we can calculate the C3 based on Equation (7).

Under the quantum resonance condition eff=4π, each matrix element of the free evolution operator Uf in angular momentum space equals to unity, i.e., Uf(n)=exp(i2πn2)=1. Consequently, the operator has no impact on the time evolution of quantum states. For one period evolution from t=tn to t=tn+1, we only need to use the kicking evolution operator to act on the quantum state, i.e., |ψ(tn+1)=UK|ψ(tn). This leads to an exact expression of a quantum state at arbitrary time t=tn in angle coordinate space, i.e., ψ(θ,tn)=UK(θ,tn)ψ(θ,t0)=exp[iKtncos(θ)/eff]ψ(θ,t0). Based on this, we can derive analytical expressions for both |ψR(t0) and |φR(t0), which yields the theoretical predictions for the OTOCs C(t).

3.1. Derivation of the Cp

Given the operators (A=p,B=p) and the quantum resonance condition, the three components of the OTOCs Cp are denoted as Cp,1(t)=ψR(t0)|p2|ψR(t0), Cp,2(t)=φR(t0)|φR(t0), and Cp,3(t)=ψR(t0)|p|φR(t0), with |ψR(t0)=UK(t)pUK(t)|ψ(t0) and |φR(t0)=UK(t)pUK(t)p|ψ(t0). At the time t=tn, the action the operator p to the state ψ(θ,tn)=UK(θ,tn)ψ(θ,t0) yields a new state ψ˜(θ,tn)=pψ(θ,tn)=sin(θ)ψ(θ,tn)Ktni4πψ(1)θ,t0expiKtncos(θ)/4π, where superscript (n) (n=1,2) denotes the n-th order derivative of the functions. We then perform the time reversal from tn to t0 starting from ψ˜(θ,tn) and obtain

ψR(θ,t0)=UK(θ,tn)ψ˜(θ,tn)=Ktnsin(θ)ψ(θ,t0)i4πψ(1)θ,t0. (8)

With this state, one can obtain the analytical expression of Cp,1(tn)

Cp,1(tn)=16π2K2tn202π|Ψθ|2dθ+256π402π|ψ(2)θ,t0|2dθ, (9)

where the function Ψ(θ) takes the forms Ψθ=ψ(θ,t0)cos(θ)+ψ(1)θ,t0sin(θ).

For the derivation of Cp,2(tn), we apply the operator p to acting on the initial state, which yields φ(θ,t0)=pψ(θ,t0)=i4πψ(1)θ,t0. Then, forward evolution from t0 to tn creates the state φ(θ,tn)=i4πψ(1)θ,t0expiKtncos(θ)/4π, along with φ˜(θ,tn)=pφ(θ,tn)=Ktnsin(θ)φ(θ,tn)i4πφ(1)θ,t0expi4πKtncos(θ). Conducting the backward evolution from tn to t0 for the state φ˜(θ,tn), we obtain

φR(θ,t0)=Ktnsin(θ)φ(θ,t0)i4πφ(1)θ,t0. (10)

With the assistance of the two states, we establish the following relations

Cp,2(tn)=16π2K2tn202π|ψ(1)θ,t0|2sin2(θ)dθ+256π402π|ψ(2)θ,t0|2dθ, (11)

and

Cp,3(tn)=16π2K2tn202πΓθdθ+i64π3Ktn02πΥ(θ)dθ256π402πψ(1)θ,t0*ψ(3)θ,t0dθ. (12)

Here, the superscript ∗ indicates the complex conjugate of the variable. The functions Γ(θ) and Υ(θ) take the forms Γθ=ψ*θ,t0sin2(θ)ψ(2)θ,t0+12sin(2θ)ψ(1)θ,t0 and Υ(θ)=sin(θ)ψ*θ,t0ψ(3)θ,t0ψ(1)θ,t0*ψ(2)θ,t0cos(θ)|ψ(1)θ,t0|2. Therefore, we can obtain the expression of the OTOCs

Cp(tn)=Cp,1(tn)+Cp,2(tn)2Re[Cp,3(tn)]=16π2K2tn202πΦθ+2ReΓθdθ+128π3Ktn02πImΥ(θ)dθ+512π402πReψ(1)θ,t0*ψ(3)θ,t0dθ+512π402π|ψ(2)θ,t0|2dθ, (13)

with Φθ=|ψ(1)θ,t0|2sin2(θ)+|Ψθ|2 and Im() indicating the imaginary part of a complex variable. It is obvious that the time dependence of Cp contains a quadratic function, determined by the integral of the functions Φθ and Γθ, and a linear function related to the integral of the function Υ(θ). The exact dependence of the functions Φθ, Γθ, and Υ(θ) on initial states, as shown above, serves as a crucial knob for controlling the behavior of OTOCs through the preparation of different starting conditions. For example, suppose we choose the initial state ψ(θ,t0)=cos(θ)/π, resulting in the equivalence

Cp(t)=12π2K2t2. (14)

3.2. Derivation of the CT

The three components of CT are represented as CT,1(t)=ψR(t0)|p2|ψR(t0), CT,2(t)=φR(t0)|φR(t0), and CT,3(t)=ψR(t0)|p|φR(t0). Here, the time-reversed states at time t0, influenced by the operators T=exp(iϵp/eff) and the initial states ψ(t0), take the forms |ψR(t0)=UK(t)exp(iϵp/eff)UK(t)|ψ(t0) and |φR(t0)=UK(t)exp(iϵp/eff)UK(t)exp(iϵp/eff)|ψ(t0), respectively. By repeating the same procedure for the derivation of both |ψR(t0) and |φR(t0) of Cp, we can obtain the exact expressions of the two states under quantum resonance condition

ψR(θ,t0)=ψθ+ϵ,t0expiKt2πsinϵ2sin2θ+ϵ2 (15)

and

φR(θ,t0)=i4πψ(1)θ+ϵ,t0expiKt2πsinϵ2sin2θ+ϵ2. (16)

Consequently, one can derive analytically the three components of the CT

CT,1(t)=4K2t2sin2ϵ202πcos2θ+ϵ2|ψθ+ϵ,t0|2dθ+16π202πψ(1)θ+ϵ,t02dθ, (17)
CT,2(t)=16π202πψ(1)θ+ϵ,t02dθ, (18)

and

CT,3(t)=i8πsinϵ2Kt02πυθdθ16π202πψ*θ+ϵ,t0ψ(2)θ+ϵ,t0dθ. (19)

with υθ=ψ*θ+ϵ,t0ψ(1)θ+ϵ,t0cos(θ+ϵ2). Combining these three parts yields

CT(t)=CT,1(t)+CT,2(t)2Re[CT,3(t)]=4K2t2sin2ϵ202πcos2θ+ϵ2|ψθ+ϵ,t0|2dθ16πsinϵ2Kt02πImυθdθ,+32π202πReψ*θ+ϵ,t0ψ(2)θ+ϵ,t0dθ,+32π202πψ(1)θ+ϵ,t02dθ. (20)

Obviously, the term of quadratic growth in the function CT is governed by the integral involving the modular square |ψθ+ϵ,t0|2. The term of the linear growth in CT depends on the integral of the function υθ, which is related to the initial state ψθ,t0. The close relationship between CT and the initial state provides the unique opportunity to engineer the OTOCs’ behavior under various initial states. For a specific form of the initial state ψ(θ,t0)=cos(θ)/π, it is straightforward to establish the relation

CT(t)=sin2ϵ22+cos(ϵ)K2t2. (21)

4. Conclusions and Discussion

In this work, we thoroughly investigate the dynamics of OTOCs, employing Cp and CT under quantum resonance conditions. The Cp quantifies the commutation relation of two angular momentum operators at different times, while the CT measures that between the translation operator and angular momentum operator at different times. Our exact deductions of the quantum states during forward evolution and time reversal under quantum resonance allow us to establish the laws governing the time dependence of OTOCs. Our findings demonstrate that both Cp and CT exhibit quadratic growth with time evolution, revealing an intrinsic power-law scrambling in their late-time behavior. Note that the mechanism of dynamical localization under non-resonant conditions suppresses quantum scrambling [27]. Therefore, the observed quadratic growth of OTOCs finds its origin in essential quantum coherence effects arising from quantum resonance, without classical analogs. We expect that the identification of similar power laws for different types of OTOCs reveals the universality in the power-law growth within the QKR model. It has been found that the delocalization effects with unique quantum coherence leads to the quadratic growth of OTOCs in the QKR model with quantum non-resonance condition [7]. Therefore, our discovery of the crucial role played by quantum coherence in facilitating quantum scrambling has significant implications in the fields of quantum information and quantum chaos [6,8,63].

Author Contributions

Investigation, G.L.; Writing—review & editing, W.Z. All authors have read and agreed to the published version of the manuscript.

Institutional Review Board Statement

Not applicable.

Data Availability Statement

No new data were created or analyzed in this study. Data sharing is not applicable to this article.

Conflicts of Interest

The authors declare no conflict of interest.

Funding Statement

This work is supported by the National Natural Science Foundation of China (Grant Nos. 12065009 and 12365002), the Natural Science Foundation of Jiangxi province (Grant Nos. 20224ACB201006 and 20224BAB201023).

Footnotes

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