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We study the out-of-equilibrium dynamics in the quantum Ising model with power-law interactions and positional disorder. For arbitrary dimension $d$ and interaction range $alpha geq d$ we analytically find a stretched exponential decay of the global magnetization and ensemble-averaged single-spin purity with a stretch-power $beta = d/alpha$ in the thermodynamic limit. Numerically, we confirm that glassy behavior persists for finite system sizes and sufficiently strong disorder. We identify dephasing between disordered coherent pairs as the main mechanism leading to a relaxation of global magnetization, whereas genuine many-body interactions lead to a loss of single-spin purity which signifies the build-up of entanglement. The emergence of glassy dynamics in the quantum Ising model extends prior findings in classical and open quantum systems, where the stretched exponential law is explained by a scale-invariant distribution of time scales, to both integrable and non-integrable quantum systems.
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Understanding the dynamics of strongly interacting disordered quantum systems is one of the most challenging problems in modern science, due to features such as the breakdown of thermalization and the emergence of glassy phases of matter. We report on the observation of anomalous relaxation dynamics in an isolated XXZ quantum spin system realized by an ultracold gas of atoms initially prepared in a superposition of two-different Rydberg states. The total magnetization is found to exhibit sub-exponential relaxation analogous to classical glassy dynamics, but in the quantum case this relaxation originates from the build-up of non-classical correlations. In both experiment and semi-classical simulations, we find the evolution towards a randomized state is independent of the strength of disorder up to a critical value. This hints towards a unifying description of relaxation dynamics in disordered isolated quantum systems, analogous to the generalization of statistical mechanics to out-of-equilibrium scenarios in classical spin glasses.
The transport of excitations governs fundamental properties of matter. Particularly rich physics emerges in the interplay between disorder and environmental noise, even in small systems such as photosynthetic biomolecules. Counterintuitively, noise can enhance coherent quantum transport, which has been proposed as a mechanism behind the high transport efficiencies observed in photosynthetic complexes. This effect has been called environmental-assisted quantum transport (ENAQT). Here, we propose a quantum simulation of the excitation transport in an open quantum network, taking advantage of the high controllability of current trapped-ion experiments. Our scheme allows for the controlled study of various different aspects of the excitation transfer, ranging from the influence of static disorder and interaction range, over the effect of Markovian and non-Markovian dephasing, to the impact of a continuous insertion of excitations. Our proposal discusses experimental error sources and realistic parameters, showing that it can be implemented in state-of-the-art ion-chain experiments.
Large-scale quantum devices provide insights beyond the reach of classical simulations. However, for a reliable and verifiable quantum simulation, the building blocks of the quantum device require exquisite benchmarking. This benchmarking of large scale dynamical quantum systems represents a major challenge due to lack of efficient tools for their simulation. Here, we present a scalable algorithm based on neural networks for Hamiltonian tomography in out-of-equilibrium quantum systems. We illustrate our approach using a model for a forefront quantum simulation platform: ultracold atoms in optical lattices. Specifically, we show that our algorithm is able to reconstruct the Hamiltonian of an arbitrary size quasi-1D bosonic system using an accessible amount of experimental measurements. We are able to significantly increase the previously known parameter precision.
Nonadiabatic molecular dynamics occur in a wide range of chemical reactions and femtochemistry experiments involving electronically excited states. These dynamics are hard to treat numerically as the systems complexity increases and it is thus desirable to have accurate yet affordable methods for their simulation. Here, we introduce a linearized semiclassical method, the generalized discrete truncated Wigner approximation (GDTWA), which is well-established in the context of quantum spin lattice systems, into the arena of chemical nonadiabatic systems. In contrast to traditional continuous mapping approaches, e.g. the Meyer-Miller-Stock-Thoss and the spin mappings, GDTWA samples the electron degrees of freedom in a discrete phase space, and thus forbids an unphysical unbounded growth of electronic state populations. The discrete sampling also accounts for an effective reduced but non-vanishing zero-point energy without an explicit parameter, which makes it possible to treat the identity operator and other operators on an equal footing. As numerical benchmarks on two Linear Vibronic Coupling models show, GDTWA has a satisfactory accuracy in a wide parameter regime, independently of whether the dynamics is dominated by relaxation or by coherent interactions. Our results suggest that the method can be very adequate to treat challenging nonadiabatic dynamics problems in chemistry and related fields.
We discuss monitoring the time evolution of an analog quantum simulator via a quantum non-demolition (QND) coupling to an auxiliary `clock qubit. The QND variable of interest is the `energy of the quantum many-body system, represented by the Hamiltonian of the quantum simulator. We describe a physical implementation of the underlying QND Hamiltonian for Rydberg atoms trapped in tweezer arrays using laser dressing schemes for a broad class of spin models. As an application, we discuss a quantum protocol for measuring the spectral form factor of quantum many-body systems, where the aim is to identify signatures of ergodic vs. non-ergodic dynamics, which we illustrate for disordered 1D Heisenberg and Floquet spin models on Rydberg platforms. Our results also provide the physical ingredients for running quantum phase estimation protocols for measurement of energies, and preparation of energy eigenstates for a specified spectral resolution on an analog quantum simulator.
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