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Journal of Applied Physics

Critical behavior of three-dimensional Ising model of spin glass (invited)

Andrew T. Ogielski, I. Morgenstern

Published Apr 15, 1985• 21 citations
Publisher

Abstract

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.

DOI
10.1063/1.335103

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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.
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.
First results of massive Monte Carlo simulations of the d=3 Ising spin-glass with \ifmmode\pm\else\textpm\fi{}J bond distribution, performed on a fast special purpose computer, are presented. A qualitative change in the behavior of the system and best fits for the spin-glass correlation length and relaxation time favor equilibrium phase transition at Tc{\mathrm{T}}_{\mathrm{c}}Tc​/J\ensuremath{\approxeq}1.2. .AE
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.
I present an analysis of the dynamic behavior of short-range Ising spin glasses observed in stochastic simulations. The time dependence of the order parameter q(t)=〈Sx{S}_{x}Sx​(0)Sx{S}_{x}Sx​(t)〉\ifmmode\bar\else\textasciimacron\fi{}---which is the same as that of the structure factor---and the time dependence of the related dynamic correlation functions have been recorded with good statistics and very long observation times. The spin-glass model with a symmetric distribution of discrete nearest-neighbor \ifmmode\pm\else\textpm\fi{}J interactions on a simple-cubic lattice was used. Simulations were performed with a special fast computer, allowing for the first-time investigation of the equilibrium dynamics for a wide range of temperatures (0.7\ensuremath{\le}kT/J\ensuremath{\le}5.0) and lattice sizes (83{8}^{3}83, 163{16}^{3}163, 323{32}^{3}323, and 643{64}^{3}643). I have found that the empirical formula q(t)=${\mathrm{ct}}^{\mathrm{\ensuremath{-}}x}$exp(-\ensuremath{\omega}${t}^{\ensuremath{\beta}}$) with temperature-dependent exponents x(T) and \ensuremath{\beta}(T) describes the decay very well at all temperatures above the spin-glass transition. In the spin-glass phase, only the algebraic decay q(t)=${\mathrm{ct}}^{\mathrm{\ensuremath{-}}x}$ could be observed, with different temperature dependences of the exponent x(T). The dynamic scaling hypothesis and finite-size scaling explain well the observed temperature and size dependence of the data, and the functional form of the correlation functions is com- patible with the scaling form if corrections to scaling are taken into account. The scaling behavior and the dynamic and static critical exponents found in my simulations are in reasonable agreement with recent experiments performed on insulating spin glasses, showing that despite its simplicity the discrete model of spin glasses analyzed in this work displays behavior similar to that seen in nature.
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.
The statics-dynamics correspondence in spin glasses relate nonequilibrium 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.