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arXiv:2607.13989

Nonreciprocal Relaxation Acceleration

Xingyu Zhang, Yihan Ma, Yue Liu, Niaz Ali Khan, Chenlong Huang, Yuguo Su, Junyan Luo, Dahai He

quant-phSubmitted Jul 15, 2026• Announced Jul 16, 2026• 0 citations
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Abstract

Driven by recent discoveries regarding the quantum Mpemba effect, the anomalous relaxation dynamics of open quantum systems have garnered significant attention. While expediting thermalization to equilibrium has been extensively studied, dynamically accelerating the convergence toward nonequilibrium steady states remains a formidable challenge. In this article, we find a transient engineered nonreciprocal dissipative channel can provide a shortcut that accelerates convergence to the target reciprocal nonequilibrium steady state for the considered two-mode model and initial states. Using interacting bosonic modes, we demonstrate that the temporal activation of a nonreciprocal channel efficiently suppresses prolonged inter-mode energy oscillations, enforcing a rapid, unidirectional thermal dump into the environment. Counterintuitively, we find that this relaxation speedup is robust and independent of the direction of the nonreciprocity. Our results provide a powerful thermodynamic technique for rapid state preparation and cooling in continuous-variable quantum systems, particularly critical for low-temperature quantum information processing.

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Driven by recent discoveries regarding the quantum Mpemba effect, the anomalous relaxation dynamics of open quantum systems have garnered significant attention. While expediting thermalization to equilibrium has been extensively studied, dynamically accelerating the convergence toward nonequilibrium steady states remains a formidable challenge. In this article, we find a transient engineered nonreciprocal dissipative channel can provide a shortcut that accelerates convergence to the target reciprocal nonequilibrium steady state for the considered two-mode model and initial states. Using interacting bosonic modes, we demonstrate that the temporal activation of a nonreciprocal channel efficiently suppresses prolonged inter-mode energy oscillations, enforcing a rapid, unidirectional thermal dump into the environment. Counterintuitively, we find that this relaxation speedup is robust and independent of the direction of the nonreciprocity. Our results provide a powerful thermodynamic technique for rapid state preparation and cooling in continuous-variable quantum systems, particularly critical for low-temperature quantum information processing.
We study the thermalization dynamics of a quantum system embedded in an incommensurate potential and coupled to a Markovian thermal reservoir. The dephasing induced by the bath drives the system toward an infinite-temperature steady state, erasing all initial information-including signatures of localization. We find that initially localized states can relax to the homogeneous steady state faster than delocalized states. Moreover, low-temperature initial states thermalize to infinite temperature more rapidly than high-temperature states---a phenomenon reminiscent of the Mpemba effect, in which hotter liquids freeze faster than colder ones. The slowest relaxation mode in the Liouvillian spectrum plays a critical role in the expedited thermalization for localized or cold initial states. Our results reveal that the combination of disordered structure and environmental dissipation may lead to nontrivial thermalization behavior, which advances both the conceptual framework of the Mpemba effect and the theoretical understanding of nonequilibrium processes in dissipative disordered systems.
We investigate the quantum Mpemba effect in the relaxation of open quantum systems whose effective dynamics is described by Davies maps. We introduce a class of unitary transformations constructed from permutation matrices that, when applied to an initial state, (i) suppress the slowest decaying modes of the nonunitary dynamics and (ii) maximize the state's distinguishability from the steady state. The first condition ensures exponentially faster convergence to equilibrium, while the second implies that a quantum system initially further from equilibrium can approach it more rapidly than one that starts closer. This protocol thus realizes a genuine Mpemba effect, and its simulation requires low computational effort. We prove that, for any initial state, there exists a permutation matrix that maximizes its distance from equilibrium with respect to a chosen information-theoretic distinguishability measure. We illustrate our findings for a two-level system, as well as for the nonunitary dynamics of the transverse-field Ising chain and the XXZ chain, each weakly coupled to a bosonic thermal bath. In these cases, the quantum Mpemba effect is demonstrated using the Hilbert-Schmidt distance, quantum relative entropy, and trace distance. Overall, our results provide a versatile framework for engineering a genuine quantum Mpemba effect in Markovian open quantum systems.
Slow relaxation processes spanning widely separated timescales pose fundamental challenges for probing steady-state properties and engineering functional quantum systems, such as quantum heat engines and quantum computing devices. We introduce a protocol that enables significant acceleration of relaxation in general Markovian open quantum systems by temporarily coupling the system to a reset channel, inspired by the Mpemba effect. Crucially, this acceleration persists even when the slowest decaying Lindbladian modes form complex-conjugate pairs. Unlike previous approaches, which typically target a single mode, our protocol may suppress multiple relaxation modes simultaneously. This framework provides a versatile and experimentally feasible tool for controlling relaxation timescales, with broad implications for quantum thermodynamics, computation, and state preparation.
The Mpemba effect, where a state farther from equilibrium relaxes faster than one closer to it, is a striking phenomenon in both classical and quantum systems. In open quantum systems, however, the quantum Mpemba effect (QME) typically occurs only for specifically chosen initial states, which limits its universality. Here we present a general and experimentally feasible strategy to realize both QME and anti-QME. By applying a temporary bond-dissipation quench, we selectively suppresses or enhances slow relaxation modes, thereby reshaping relaxation pathways independently of both the system and the initial state. We demonstrate this mechanism in systems with dephasing and boundary dissipation, and outline feasible cold-atom implementations. Our results establish controllable dissipation as a versatile tool for quantum control, accelerated relaxation, and efficient nonequilibrium protocols.
The behavior of systems far from equilibrium is often complex and unpredictable, challenging and sometimes overturning the physical intuition derived from equilibrium scenarios. One striking example of this is the Mpemba effect, which implies that non-equilibrium states can sometimes relax more rapidly when they are further from equilibrium. Despite a rich historical background, the precise conditions and mechanisms behind this phenomenon remain unclear. Recently, there has been growing interest in investigating accelerated relaxation and Mpemba-like effects within quantum systems. In this work, we explore a quantum manifestation of the Mpemba effect in a simple and paradigmatic model of open quantum systems: the damped quantum harmonic oscillator, which describes the relaxation of a bosonic mode in contact with a thermal bath at finite temperature T . By means of an exact analytical analysis of the relaxation dynamics based on the method of moments in both population and coherence subspaces, we demonstrate that any initial distribution of populations with the first r moments exactly matching those of the equilibrium distribution shows a super-accelerated relaxation to equilibrium at a rate linearly increasing with r , leading to a pronounced Mpemba effect. In particular, one can find a broad class of far-from-equilibrium distributions that relax to equilibrium faster than any other initial thermal state with a temperature T ′ arbitrarily close to T . The super-accelerated relaxation effect is shown to persist even for a broad class of initial states with non-vanishing coherences, and a general criterion for the observation of super-accelerated thermalization is presented.
Quantum thermometry provides a key capability for nanoscale devices and quantum technologies, but most existing strategies rely on probes initialized near equilibrium. This equilibrium paradigm imposes intrinsic limitations: sensitivity is tied to long-time thermalization and often cannot be improved in fast, noisy, or nonstationary settings. In contrast, the \textit{Mpemba effect}, the counterintuitive phenomenon where hotter states relax faster than colder ones, has mostly been viewed as a thermodynamic anomaly. Here, we bridge this gap by proving that Mpemba-type inversions generically yield a finite-time enhancement of the quantum Fisher information (QFI) for temperature estimation, thereby converting an anomalous relaxation effect into a concrete metrological resource. Through explicit analyses of two-level and ΛΛΛ-level probes coupled to bosonic baths, we show that nonequilibrium initializations can transiently outperform both equilibrium strategies and colder states, realizing a \emph{metrological Mpemba effect}. Our results establish anomalous relaxation as a general design principle for nonequilibrium quantum thermometry, enabling ultrafast and nanoscale sensing protocols that exploit, rather than avoid, transient dynamics.