We have studied numerically the dynamics of spin glasses with Ising and
XY symmetry (gauge glass) in space dimensions 2, 3, and 4. The nonequilibrium spin-glass susceptibility ${\ensuremath{\chi}}_{\mathrm{ne}}({t}_{\mathrm{w}},T)$ and the nonequilibrium energy per spin,
ene(tw,T), of samples of large size
Lb are measured as a function of anneal time
tw after a quench to temperatures
T. The two observables are compared to the equilibrium spin-glass susceptibility ${\ensuremath{\chi}}_{\mathrm{eq}}(L,T)$ and the equilibrium energy
eeq(L,T), respectively, measured as functions of temperature
T and system size
L for a range of system sizes. For any time and temperature a nonequilibrium time-dependent length scale
L∗(tw,T) can be defined by writing ${\ensuremath{\chi}}_{\mathrm{ne}}({t}_{\mathrm{w}},T)={\ensuremath{\chi}}_{\mathrm{eq}}({L}^{*},T)$ (or the equivalent expression for the energy). Our analysis shows that for all systems studied, an ``effective dynamical critical exponent'' parametrization
L∗(tw,T)=A(T)t1∕z(T) fits the data well at each temperature within the whole temperature range studied, which extends from well above the critical temperature
Tc to near
T=0 for dimension 2 or to well below
Tc for the other space dimensions studied. In addition, the data suggest that the dynamical exponent
z varies smoothly when crossing the transition temperature.
We study the dynamics of excitations in a system of
O(N) quantum rotors in the presence of random fields and random anisotropies. Below the lower critical dimension
dlc=4 the system exhibits a quasi-long-range order with a power-law decay of correlations. At zero temperature the spin waves are localized at the length scale
Lloc beyond which the quantum tunneling is exponentially suppressed, $c\ensuremath{\sim}{e}^{\ensuremath{-}{(L/{L}_{\mathrm{loc}})}^{2(\ensuremath{\theta}+1)}}$. At finite temperature
T the spin waves propagate by thermal activation over energy barriers that scale as ${L}^{\ensuremath{\theta}}$. Above
dlc the system undergoes an order-disorder phase transition with activated dynamics such that the relaxation time grows with the correlation length $\ensuremath{\xi}$ as $\ensuremath{\tau}\ensuremath{\sim}{e}^{C{\ensuremath{\xi}}^{\ensuremath{\theta}}/T}$ at finite temperature and as $\ensuremath{\tau}\ensuremath{\sim}{e}^{{C}^{\ensuremath{'}}{\ensuremath{\xi}}^{2(\ensuremath{\theta}+1)}/{\ensuremath{\hbar}}^{2}}$ in the vicinity of the quantum critical point.
We present results of a Monte Carlo simulation study of the zero-temperature quantum phase transition of a three-dimensional short-range spin-1/2 Ising spin glass, driven by a transverse magnetic field. This quantum transition is equivalent to the finite-temperature transition in the (3+1)-dimensional anisotropic classical random Ising model that is the path integral of the quantum system. The critical exponents are estimated using a finite-size scaling analysis. The uniform linear susceptibility is finite at the transition, while the nonlinear susceptibility diverges. The results are more consistent with conventional, rather than activated, dynamic scaling in the quantum system.
We study the dynamical melting of hot one-dimensional quantum glasses. We focus on quantum glasses that emerge at strong disorder: specifically, many-body localized systems and their critical variants. The latter category includes disordered Ising, Potts, and anyonic chains whose excited-state properties and dynamics can be accessed via real-space renormalization group methods. As disorder is weakened below a critical value these non-thermal quantum glasses melt via a continuous dynamical phase transition into a classical thermal liquid. By accounting for resonant tunneling of energy, we derive and solve an effective model for such quantum-to-classical transitions and compute their universal critical properties. Notably, the classical thermal liquid exhibits a broad regime of anomalously slow sub-diffusive equilibration dynamics and energy transport, crossing over to ordinary classical diffusion at asymptotically long length scales for critical glasses. The subdiffusive regime is characterized by a continuously evolving dynamical critical exponent that diverges with a universal power at the transition. For non-critical, many-body localized glasses, the crossover scale diverges and subdiffusion persists to the thermodynamic limit. Our approach provides a firm microscopic basis for understanding the generic structure of many-body delocalization transitions in one dimension, and also reveals a general scaling relation among the critical exponents of the transition.