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arXiv:2506.15108 · Physical review. B./Physical review. B

Aperiodic dissipation as a mechanism for steady-state localization

Shilpi Roy, Jiangbin Gong

Published Sep 22, 2025• 3 citations
arXivHTMLPDF

Abstract

Dissipation is traditionally regarded as a disruptive factor in quantum systems because it often leads to decoherence and delocalization. However, recent insights into engineered dissipation reveal that it can be tuned to facilitate various quantum effects, from state stabilization to phase transitions. In this work, we identify aperiodic dissipation as a mechanism for inducing steady-state localization, independent of disorder or a quasiperiodic potential in the Hamiltonian. This localization arises from long-range phase correlations introduced by a spatially varying dissipation phase parameter, which enables nontrivial interference in the steady state. By systematically comparing two classes of aperiodic dissipation (defined as commensurate and incommensurate cases), we conclude that both can lead to localization in the thermodynamic limit. Our analysis, based on coherence measures, purity, and participation ratio, reveals a direct link between eigenstate coherence and real-space localization, showing that dissipation can actively shape localization rather than simply causing decoherence. These findings highlight aperiodic dissipation as a viable approach to controlling localization in open quantum systems, potentially enabling new ways to manipulate quantum states and design dissipation-driven phases.

DOI
10.1103/qprv-gf5g

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Dissipation is traditionally regarded as a disruptive factor in quantum systems because it often leads to decoherence and delocalization. However, recent insights into engineered dissipation reveal that it can be tuned to facilitate various quantum effects, from state stabilization to phase transitions. In this work, we identify aperiodic dissipation as a mechanism for inducing steady-state localization, independent of disorder or a quasiperiodic potential in the Hamiltonian. This localization arises from long-range phase correlations introduced by a spatially varying dissipation phase parameter, which enables nontrivial interference in the steady state. By systematically comparing two classes of aperiodic dissipation (defined as commensurate and incommensurate cases), we conclude that both can lead to localization in the thermodynamic limit. Our analysis, based on coherence measures, purity, and participation ratio, reveals a direct link between eigenstate coherence and real-space localization, showing that dissipation can actively shape localization rather than simply causing decoherence. These findings highlight aperiodic dissipation as a viable approach to controlling localization in open quantum systems, potentially enabling new ways to manipulate quantum states and design dissipation-driven phases.
The interplay between dissipation and localization in quantum systems has garnered significant attention due to its potential to manipulate transport properties and induce phase transitions. In this work, we explore the dissipation-induced extended-localized transition in a flat band model, where the system's asymptotic state can be controlled by tailored dissipative operators. By analyzing the steady-state density matrix and dissipative dynamics, we demonstrate that dissipation is able to drive the system to states dominated by either extended or localized modes, irrespective of the initial conditions. The control mechanism relies on the phase properties of the dissipative operators, which selectively favor specific eigenstates of the Hamiltonian. Our findings reveal that dissipation can be harnessed to induce transitions between extended and localized phases, offering a novel approach to manipulate quantum transport in flat band systems. This work not only deepens our understanding of dissipation-induced phenomena in flat band systems but also provides a new avenue for controlling quantum states in open systems.
Dissipation is usually regarded as a source of decoherence that suppresses quantum interference and localization. Here we show that suitably engineered dissipation can instead be used to select localized or extended states in a strictly non-disordered one-dimensional lattice. The underlying clean lattice has spatially inhomogeneous hopping and supports both extended bulk states and localized boundary states, including an algebraically localized bound state in the continuum. We introduce a nonlocal bond jump operator with a tunable relative phase and show that this phase selectively favors eigenstates with different spatial phase correlations. As a result, the long-time density matrix can be steered toward sectors dominated by localized or extended Hamiltonian eigenstates without changing any Hamiltonian parameter. The microscopic origin of the selection is quantified by the fraction of site pairs separated by a distance lll that are phase matched with the dissipative channel. We further characterize the dissipative quench through the quantum fidelity and show that the selected character of the steady state can persist after the dissipation is removed. Our results establish phase-selective bond dissipation as a route to controllable state preparation and transport manipulation in non-disordered lattices.
The interplay between dissipation and localization in quantum systems has garnered significant attention due to its potential to manipulate transport properties and induce phase transitions. In this work, we explore the dissipation-induced extended-localized transition in a flat-band model, where the system's asymptotic state can be controlled by tailored dissipative operators. By analyzing the steady-state density matrix and dissipative dynamics, we demonstrate that dissipation is able to drive the system to states dominated by either extended or localized modes, irrespective of the initial conditions. The control mechanism relies on the phase properties of the dissipative operators, which selectively favor specific Hamiltonian eigenstates. Our findings reveal that dissipation can be harnessed to induce transitions between extended and localized phases, offering a novel approach to manipulate quantum transport in flat-band systems. This work not only deepens our understanding of dissipation-induced phenomena in flat-band systems but also provides a new avenue for controlling quantum states in open systems.
The quest for nonequilibrium quantum phase transitions is often hampered by the tendency of driving and dissipation to give rise to an effective temperature, resulting in classical behavior. Could this be different when the dissipation is engineered to drive the system into a nontrivial quantum coherent steady state? In this work we shed light on this issue by studying the effect of disorder on recently introduced dissipation-induced Chern topological states, and examining the eigenmodes of the Hermitian steady-state density matrix or entanglement Hamiltonian. We find that, similarly to equilibrium, each Landau band has a single delocalized level near its center. However, using three different finite-size scaling methods we show that the critical exponent $\ensuremath{\nu}$ describing the divergence of the localization length upon approaching the delocalized state is significantly different from equilibrium if disorder is introduced into the nondissipative part of the dynamics. This indicates a different type of nonequilibrium quantum critical universality class accessible in cold-atom experiments.
We study a one-dimensional quasiperiodic tight-binding model with simultaneous off-diagonal (hopping) and diagonal (onsite) modulations. Using the inverse participation ratio and the wave-packet centroid, we construct localization-delocalization phase diagrams for both equilibrium and nonequilibrium steady states. We analyze the robustness of initial-state properties under dissipation and characterize dissipation-induced localization-delocalization transitions (and their reversals) in detail. Trace-distance dynamics provide evidence for a quantum Mpemba effect: states prepared farther from the steady state can relax faster than states initialized closer to it. We propose a starting-line hypothesis that explains the presence or absence of this effect across parameter regimes. These results advance the understanding of steady-state phase transitions and relaxation dynamics in dissipatively driven quasiperiodic systems.
Anderson localization and the mobility edge (ME) have been extensively studied in isolated aperiodic systems. Conventional theory suggests that dephasing and decoherence should disrupt localization and facilitate transport. In this work, we investigate localization behaviors in a dimerized off-diagonal Aubry-Andre-Harper (AAH) quasicrystal subject to on-site pure dephasing. In the strong-dephasing limit, we apply adiabatic elimination within the Lindblad master equation framework to derive an effective classical Markov transition matrix that governs the dissipative relaxation dynamics. Counterintuitively, we demonstrate that pure dephasing can induce distinct MEs, including both conventional MEs separating extended and localized states and anomalous MEs separating multifractal critical states from localized states, even when all eigenstates of the original closed coherent system are delocalized or multifractal. Using fractal dimension finite-size scaling, wave-packet spreading dynamics, and energy spectrum statistics, we numerically verify the coexistence of fully extended, multifractal critical, and localized regions within the relaxation spectrum of the dissipative system, and construct the global dissipative phase diagram. These findings reveal that dephasing can see as a powerful mechanism for controlling localization transitions, thus enhancing our understanding of dissipative quasicrystal systems.