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arXiv:2209.09297 · Physical Review Letters

Controlling Local Thermalization Dynamics in a Floquet-Engineered Dipolar Ensemble

Leigh S. Martin, Hengyun Zhou, Nathaniel Leitao, Nishad Maskara, Oksana Makarova, Haoyang Gao, Qian-Ze Zhu, Mincheol Park, Matthew Tyler, Hongkun Park, Soonwon Choi, Mikhail D. Lukin

Published May 25, 2023• 22 citations
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Abstract

Understanding the microscopic mechanisms of thermalization in closed quantum systems is among the key challenges in modern quantum many-body physics. We demonstrate a method to probe local thermalization in a large-scale many-body system by exploiting its inherent disorder and use this to uncover the thermalization mechanisms in a three-dimensional, dipolar-interacting spin system with tunable interactions. Utilizing advanced Hamiltonian engineering techniques to explore a range of spin Hamiltonians, we observe a striking change in the characteristic shape and timescale of local correlation decay as we vary the engineered exchange anisotropy. We show that these observations originate from the system's intrinsic many-body dynamics and reveal the signatures of conservation laws within localized clusters of spins, which do not readily manifest using global probes. Our method provides an exquisite lens into the tunable nature of local thermalization dynamics and enables detailed studies of scrambling, thermalization, and hydrodynamics in strongly interacting quantum systems.

DOI
10.1103/physrevlett.130.210403

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Understanding the microscopic mechanisms of thermalization in closed quantum systems is among the key challenges in modern quantum many-body physics. We demonstrate a method to probe local thermalization in a large-scale many-body system by exploiting its inherent disorder and use this to uncover the thermalization mechanisms in a three-dimensional, dipolar-interacting spin system with tunable interactions. Utilizing advanced Hamiltonian engineering techniques to explore a range of spin Hamiltonians, we observe a striking change in the characteristic shape and timescale of local correlation decay as we vary the engineered exchange anisotropy. We show that these observations originate from the system's intrinsic many-body dynamics and reveal the signatures of conservation laws within localized clusters of spins, which do not readily manifest using global probes. Our method provides an exquisite lens into the tunable nature of local thermalization dynamics and enables detailed studies of scrambling, thermalization, and hydrodynamics in strongly interacting quantum systems.
Understanding the thermalization dynamics of quantum many-body systems at the microscopic level is among the central challenges of modern statistical physics. Here we experimentally investigate individual spin dynamics in a two-dimensional ensemble of electron spins on the surface of a diamond crystal. We use a near-surface nitrogen-vacancy center as a nanoscale magnetic sensor to probe correlation dynamics of individual spins in a dipolar interacting surface spin ensemble. We observe that the relaxation rate for each spin is significantly slower than the naïve expectation based on independently estimated dipolar interaction strengths with nearest neighbors and is strongly correlated with the timescale of the local magnetic field fluctuation. We show that this anomalously slow relaxation rate is due to the presence of strong dynamical disorder and present a quantitative explanation based on dynamic resonance counting. Finally, we use resonant spin-lock driving to control the effective strength of the local magnetic fields and reveal the role of the dynamical disorder in different regimes. Our work paves the way towards microscopic study and control of quantum thermalization in strongly interacting disordered spin ensembles.
One of the central challenges of modern statistical physics is understanding the thermalization dynamics of quantum many-body systems at the microscopic level. In this thesis, we describe an experimental study of individual spin dynamics in a two-dimensional ensemble of electron spins on the surface of a diamond crystal. A near-surface NV center is used as a nanoscale magnetic sensor to probe individual spin correlation dynamics in a dipolar interacting spin ensemble. For each spin, the rate of relaxation of spin projection along the bias magnetic field is consistently much slower than the dipolar interaction strengths with its nearest neighbors and is strongly correlated with the timescale of the local magnetic field fluctuation. We present a quantitative model based on dynamic resonance counting arguments that explains these observations. Furthermore, we use resonant spin-lock driving to control the effective strength of the local magnetic fields and demonstrate the role of dynamical disorder in different regimes. In the regime of suppressed extrinsic disorder, we use dynamic mean field methods to explain our experimental observations. The work presented in this thesis paves the way towards a microscopic study of quantum thermalization in two-dimensional strongly interacting disordered spin ensembles.
Statistical mechanics underlies our understanding of macroscopic quantum systems. It is based on the assumption that out-of-equilibrium systems rapidly approach their equilibrium states, forgetting any information about their microscopic initial conditions. This fundamental paradigm is challenged by disordered systems, in which a slowdown or even absence of thermalization is expected. We report the observation of critical thermalization in a three dimensional ensemble of ∼10^{6} electronic spins coupled via dipolar interactions. By controlling the spin states of nitrogen vacancy color centers in diamond, we observe slow, subexponential relaxation dynamics and identify a regime of power-law decay with disorder-dependent exponents; this behavior is modified at late times owing to many-body interactions. These observations are quantitatively explained by a resonance counting theory that incorporates the effects of both disorder and interactions.
We investigate thermalization dynamics of a driven dipolar many-body quantum system through the stability of discrete time crystalline order. Using periodic driving of electronic spin impurities in diamond, we realize different types of interactions between spins and demonstrate experimentally that the interplay of disorder, driving, and interactions leads to several qualitatively distinct regimes of thermalization. For short driving periods, the observed dynamics are well described by an effective Hamiltonian which sensitively depends on interaction details. For long driving periods, the system becomes susceptible to energy exchange with the driving field and eventually enters a universal thermalizing regime, where the dynamics can be described by interaction-induced dephasing of individual spins. Our analysis reveals important differences between thermalization of long-range Ising and other dipolar spin models.
Understanding how closed quantum systems dynamically approach thermal equilibrium presents a major unresolved problem in statistical physics. Generically, non-integrable quantum systems are expected to thermalize as they comply with the Eigenstate Thermalization Hypothesis. However, in the presence of strong disorder, the dynamics can possibly slow down to a degree that systems fail to thermalize on experimentally accessible timescales, as in spin glasses or many-body localized systems. In general, particularly in long-range interacting quantum systems, the specific nature of the disorder necessary for the emergence of a prethermal, metastable state--distinctly separating the timescales of initial relaxation and subsequent slow thermalization--remains an open question. We study an ensemble of Heisenberg spins with a tunable distribution of random coupling strengths realized by a Rydberg quantum simulator. We observe a drastic change in the late-time magnetization when increasing disorder strength. The data is well described by models based on pairs of strongly interacting spins, which are treated as thermal for weak disorder and isolated for strong disorder. Our results indicate a crossover into a pair-localized prethermal regime in a closed quantum system of thousands of spins in the critical case where the exponent of the power law interaction matches the spatial dimension.
There has been a surge of interest in studying truly nonequilibrium quantum many-body phenomena, motivated both by theoretical advances such as in the understanding of many-body-localization (MBL), and by experimental advances in controlling synthetic quantum systems that serve as rich playgrounds to probe these phenomena. In this thesis, we show that looking at the physical structure of quantum systems, such as the locality of Hamiltonians and the entanglement of quantum states -- concepts with a quantum informational flavor to them -- is a useful lens with which to explore nonequilibrium many-body physics. We use these ideas to study localization -- the breakdown of ergodicity in certain classes of many-body systems, and also the timescales of thermalization in periodically driven many-body systems. We also explain the recent observations in a dipolar system of the discrete time crystal phase, an exemplary nonequilibrium phase of matter, and further consider the dynamics of entanglement in many-body systems.