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The Letter by N. Y. Yao et. al. [1,2] presents three models for realizing a many-body localized discrete time-crystal (MBL DTC): a short-ranged model [1], its revised version [2], as well as a long-range model of a trapped ion experiment [1,3]. We show that none of these realize an MBL DTC for the parameter ranges quoted in Refs. [1,2]. The central phase diagrams in [1] therefore cannot be reproduced. The models show rapid decay of oscillations from generic initial states, in sharp contrast to the robust period doubling dynamics characteristic of an MBL DTC. Long-lived oscillations from special initial states (such as polarized states) can be understood from the familiar low-temperature physics of a static transverse field Ising model, rather than the nonequilibrium physics of an eigenstate-ordered MBL DTC. Our results on the long-range model also demonstrate, by extension, the absence of an MBL DTC in the trapped ion experiment of Ref. [3].
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This is a reply to the comment from Khemani, Moessner and Sondhi (KMS) [arXiv:2109.00551] on our manuscript [Phys. Rev. Lett. 118, 030401 (2017)]. The main new claim in KMS is that the short-ranged model does not support an MBL DTC phase. We show that, even for the parameter values they consider and the system sizes they study, the claim is an artifact of an unusual choice of range for the crucial plots. Conducting a standard finite-size scaling analysis on the same data strongly suggests that the system is in fact a many-body localized (MBL) discrete time crystal (DTC). Furthermore, we have carried out additional simulations at larger scales, and provide an analytic argument, which fully support the conclusions of our original paper. We also show that the effect of boundary conditions, described as essential by KMS, is exactly what one would expect, with boundary effects decreasing with increasing system size. The other points in KMS are either a rehashing of points already in the literature (for the long-ranged model) or are refuted by a proper finite-size scaling analysis.
Despite being forbidden in equilibrium, spontaneous breaking of time translation symmetry can occur in periodically driven, Floquet systems with discrete time-translation symmetry. The period of the resulting discrete time crystal is quantized to an integer multiple of the drive period, arising from a combination of collective synchronization and many body localization. Here, we consider a simple model for a one dimensional discrete time crystal which explicitly reveals the rigidity of the emergent oscillations as the drive is varied. We numerically map out its phase diagram and compute the properties of the dynamical phase transition where the time crystal melts into a trivial Floquet insulator. Moreover, we demonstrate that the model can be realized with current experimental technologies and propose a blueprint based upon a one dimensional chain of trapped ions. Using experimental parameters (featuring long-range interactions), we identify the phase boundaries of the ion-time-crystal and propose a measurable signature of the symmetry breaking phase transition.
We define topological time crystals, a dynamical phase of periodically driven quantum many-body systems capturing the coexistence of topological order with the spontaneous breaking of discrete time-translation symmetry. We show that many-body localization can stabilize this phase against generic perturbations and establish some of its key features and signatures. We link topological and ordinary time crystals through three complementary perspectives: higher-form symmetries, quantum error-correcting codes, and a holographic correspondence. We also propose an experimental realization of a surface-code-based topological time crystal for the Google Sycamore processor.
Progress in the understanding of quantum critical properties of itinerant electrons has been hindered by the lack of effective models which are amenable to controlled analytical and numerically exact calculations. Here we establish that the disorder driven semimetal to metal quantum phase transition of three dimensional massless Dirac fermions could serve as a paradigmatic toy model for studying itinerant quantum criticality, which is solved in this work by exact numerical and approximate field theoretic calculations. As a result, we establish the robust existence of a non-Gaussian universality class, and also construct the relevant low energy effective field theory that could guide the understanding of quantum critical scaling for many strange metals. Using the kernel polynomial method (KPM), we provide numerical results for the calculated dynamical exponent ($z$) and correlation length exponent ($ u$) for the disorder-driven semimetal (SM) to diffusive metal (DM) quantum phase transition at the Dirac point for several types of disorder, establishing its universal nature and obtaining the numerical scaling functions in agreement with our field theoretical analysis.
By using very general arguments, we show that the entropy loss conjecture at the glass transition violates the second law of thermodynamics and must be rejected.
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