As an analysis of equilibrium phase transitions, the nonequilibrium relaxation method is extended to the spin glass (SG) transition. The $\ifmmode\pm\else\textpm\fi{}J$ Ising SG model is analyzed for three-dimensional (cubic) lattices up to the linear size of
L=127 and for four-dimensional (hypercubic) lattice up to
L=41. These sizes of systems are quite large as compared with those calculated, so far, by equilibrium simulations. As a dynamical order parameter, we calculate the clone correlation function (CCF) ${Q(t,t}_{\mathrm{w}})\ensuremath{\equiv}[〈{S}_{i}^{(1)}{(t+t}_{\mathrm{w}}){S}_{i}^{(2)}{(t+t}_{\mathrm{w}}){〉}^{\mathrm{F}}],$ which is a spin correlation of two replicas produced after the waiting time
tw from a simple starting state. It is found that the CCF shows an exponential decay in the paramagnetic phase, and a power-law decay after aginglike development $(t\ensuremath{\gg}{t}_{\mathrm{w}})$ in the SG phase. This provides a reliable upper bound of the transition temperature
Tg. It is also found that a scaling relation, ${Q(t,t}_{\mathrm{w}}{)=t}_{\mathrm{w}}^{\ensuremath{-}{\ensuremath{\lambda}}_{q}}\overline{q}{(t/t}_{\mathrm{w}}),$ holds just around the transition point providing the lower bound of
Tg. Together with these two bounds, we propose a new dynamical way for the estimation of
Tg from much larger systems. In the SG phase, the power-law behavior of the CCF for $t\ensuremath{\gg}{t}_{\mathrm{w}}$ suggests that the SG phase in short-range Ising models has a rugged phase space.
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.
The statics-dynamics correspondence in spin glasses relate non-equilibrium results on large samples (the experimental realm) with equilibrium quantities computed on small systems (the typical arena for theoretical computations). Here we employ statics-dynamics equivalence to study the Ising spin-glass critical behavior in three dimensions. By means of Monte Carlo simulation, we follow the growth of the coherence length (the size of the glassy domains), on lattices too large to be thermalized. Thanks to the large coherence lengths we reach, we are able to obtain accurate results in excellent agreement with the best available equilibrium computations. To do so, we need to clarify the several physical meanings of the dynamic exponent close to the critical temperature.
We describe results of Monte Carlo simulation studies on the Ising spin glass in four dimensions on a hypercubic lattice with nearest neighbor bonds. Studies of the equilibrium static properties show that the system undergoes a genuine phase transition to an ordered spin glass phase. Critical dynamical behavior is analyzed to obtain the dynamic exponent. Finally, we describe results on the spin glass phase, in particular the finite size scaling of the order parameter distribution function, and compare it with existing models of the spin glass phase, namely the droplet model and the Parisi solution for the low temperature phase of the infinite range spin glass.
First results of massive Monte Carlo simulations of the d=3 Ising spin glass with ± J bond distribution, performed on a fast special purpose computer, are discussed. Equilibrium static and dynamic correlation functions have been recorded for temperatures T/J=1.10 to 2.00. A qualitative change in the behavior of the system, and the best fits for the spin glass correlation length and relaxation time favor a continuous phase transition at Tc/J≊1.20±0.05. We find no evidence for the Tc=0 freezing picture.
We report a high-precision finite-size scaling study of the critical behavior of the three-dimensional Ising Edwards-Anderson model (the Ising spin glass). We have thermalized lattices up to
L=40 using the Janus dedicated computer. Our analysis takes into account leading-order corrections to scaling. We obtain
Tc=1.1019(29) for the critical temperature, $\ensuremath{\nu}=2.562(42)$ for the thermal exponent, $\ensuremath{\eta}=\ensuremath{-}0.3900(36)$ for the anomalous dimension, and $\ensuremath{\omega}=1.12(10)$ for the exponent of the leading corrections to scaling. Standard (hyper)scaling relations yield $\ensuremath{\alpha}=\ensuremath{-}5.69(13)$, $\ensuremath{\beta}=0.782(10)$, and $\ensuremath{\gamma}=6.13(11)$. We also compute several universal quantities at
Tc.