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Register a new userDepolarization dynamics in a strongly interacting solid-state spin ensemble
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We study the depolarization dynamics of a dense ensemble of dipolar interacting spins, associated with nitrogen-vacancy centers in diamond. We observe anomalously fast, density-dependent, and non-exponential spin relaxation. To explain these observations, we propose a microscopic model where an interplay of long-range interactions, disorder, and dissipation leads to predictions that are in quantitative agreement with both current and prior experimental results. Our results pave the way for controlled many-body experiments with long-lived and strongly interacting ensembles of solid-state spins.
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Conventional wisdom holds that macroscopic classical phenomena naturally emerge from microscopic quantum laws. However, despite this mantra, building direct connections between these two descriptions has remained an enduring scientific challenge. In particular, it is difficult to quantitatively predict the emergent classical properties of a system (e.g. diffusivity, viscosity, compressibility) from a generic microscopic quantum Hamiltonian. Here, we introduce a hybrid solid-state spin platform, where the underlying disordered, dipolar quantum Hamiltonian gives rise to the emergence of unconventional spin diffusion at nanometer length scales. In particular, the combination of positional disorder and on-site random fields leads to diffusive dynamics that are Fickian yet non-Gaussian. Finally, by tuning the underlying parameters within the spin Hamiltonian via a combination of static and driven fields, we demonstrate direct control over the emergent spin diffusion coefficient. Our work opens the door to investigating hydrodynamics in many-body quantum spin systems.
Quantum metrology makes use of coherent superpositions to detect weak signals. While in principle the sensitivity can be improved by increasing the density of sensing particles, in practice this improvement is severely hindered by interactions between them. Using a dense ensemble of interacting electronic spins in diamond, we demonstrate a novel approach to quantum metrology. It is based on a new method of robust quantum control, which allows us to simultaneously eliminate the undesired effects associated with spin-spin interactions, disorder and control imperfections, enabling a five-fold enhancement in coherence time compared to conventional control sequences. Combined with optimal initialization and readout protocols, this allows us to break the limit for AC magnetic field sensing imposed by interactions, opening a promising avenue for the development of solid-state ensemble magnetometers with unprecedented sensitivity.
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.
The eigenstate thermalisation hypothesis (ETH) is a statistical characterisation of eigen-energies, eigenstates and matrix elements of local operators in thermalising quantum systems. We develop an ETH-like ansatz of a partially thermalising system composed of a spin-1/2 coupled to a finite quantum bath. The spin-bath coupling is sufficiently weak that ETH does not apply, but sufficiently strong that perturbation theory fails. We calculate (i) the distribution of fidelity susceptibilities, which takes a broadly distributed form, (ii) the distribution of spin eigenstate entropies, which takes a bi-modal form, (iii) infinite time memory of spin observables, (iv) the distribution of matrix elements of local operators on the bath, which is non-Gaussian, and (v) the intermediate entropic enhancement of the bath, which interpolates smoothly between zero and the ETH value of $log 2$. The enhancement is a consequence of rare many-body resonances, and is asymptotically larger than the typical eigenstate entanglement entropy. We verify these results numerically and discuss their connections to the many-body localisation transition.
The discrete time crystal (DTC) is a recently discovered phase of matter that spontaneously breaks time-translation symmetry. Disorder-induced many-body-localization is required to stabilize a DTC to arbitrary times, yet an experimental investigation of this localized regime has proven elusive. Here, we observe the hallmark signatures of a many-body-localized DTC using a novel quantum simulation platform based on individually controllable $^{13}$C nuclear spins in diamond. We demonstrate the characteristic long-lived spatiotemporal order and confirm that it is robust for generic initial states. Our results are consistent with the realization of an out-of-equilibrium Floquet phase of matter and establish a programmable quantum simulator based on solid-state spins for exploring many-body physics.
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