Theory for the dynamics of clusters near the critical point. I. Relaxation of the Glauber kinetic Ising model

Abstract

A semiphenomenological theory is developed for dynamic critical properties, which is not limited to small deviations from equilibrium. Explicit numerical expressions are derived for linear and nonlinear response functions of the kinetic Ising model, which are compatible with dynamic scaling and recent calculations of dynamic critical exponents. An uniaxial magnet (or Ising system) and its critical fluctuations are approximated by a or cluster model, the critical part of the free energy being the sum of the contributions of clusters each containing $l$ spins. These clusters are assumed to grow and shrink with a phenomenological rate $\ensuremath{\propto}{l}^{r}$, $r\ensuremath{\approx}1$. These rates are compatible with direct Monte Carlo simulations in two and three dimensions. The resulting reaction and diffusion equation is an approximation to the master equation of the Glauber kinetic Ising model (in which the magnetization is not conserved), and has the same structure as used in nucleation theories. In linear response to space- and time-dependent fields the relaxation times of energy and magnetization are expressed as triple integrals. All relaxation times diverge as ${|1\ensuremath{-}\frac{T}{{T}_{c}}|}^{\ensuremath{-}(2\ensuremath{-}r)\ensuremath{\beta}\ensuremath{\delta}}$. This treatment is consistent with dynamic scaling and universality, and is more general than the conventional (Van Hove) theory of critical slowing down. Also the (smaller) exponents found for the response to localized variations (autocorrelation functions) agree with dynamic scaling. The wave-vector dependence of the relaxation times arises from the static correlation function only, and not from the diffusion term. If the equilibrium distribution is assumed to be that of the Fisher droplet model, and for special values of $r$, the (discrete) eigenvalue spectrum and eigenfunctions (generalized Laguerre polynomials) of the reaction equation are found explicitly. Relaxation functions and frequency-dependent susceptibilities are expressed by hypergeometric series, even in the case of nonlinear response. At the critical point, the spectrum becomes continuous and the exponential decay for large times is replaced by power-law behavior. Similarly, it is found that dynamic scaling applies also to the nucleation rate for this model, and the scaling exponent of the nucleation rate is $2\ensuremath{-}\ensuremath{\alpha}+(2\ensuremath{-}r)\ensuremath{\beta}\ensuremath{\delta}$.