Nonuniversal dynamic critical exponents are obtained for both the Glauber and Kawasaki dynamics of the Ising chain with alternating near-neighbor interactions,
J1,
J2, with the exponents related to the ratio of the two interaction strengths. We expand upon the recent work of Droz et al. [Phys. Lett. 115A, 448 (1986)] for the ferromagnetic system (
J1>0,
J2>0). For Glauber (spin-flip) dynamics we obtain the exact exponent z=1+\ensuremath{\rho} (\ensuremath{\rho}\ensuremath{\equiv}\ensuremath{\Vert}
J1/
J2\ensuremath{\Vert}) which generalizes the result of Droz et al. and is valid irrespective of the signs of
J1 and
J2, where it is assumed that \ensuremath{\Vert}
J1\ensuremath{\Vert}>\ensuremath{\Vert}
J2\ensuremath{\Vert} (\ensuremath{\rho}\ensuremath{\ge}1). For Kawasaki (spin-exchange) dynamics, we obtain dynamic critical exponents from conventional theory which provides a rigorous lower bound for the exponent z. For the case of the conserved (ferromagnetic) order parameter, however, we present arguments that the conventional exponent is exact. We obtain z=4+\ensuremath{\rho} in this case. For
J1>0,${J}_{2}$0 we derive the conventional exponent z=1+\ensuremath{\rho}, whereas for ${J}_{1}$0 we find z=2 irrespective of
J2. A key aspect of this system is the narrowing of the dynamic critical region as compared with the isotropic system (
J1=
J2). The extra bond periodicity splits the isotropic order parameter into components such that only comparatively closer to criticality does the order parameter become the dominant slow mode. The nonuniversal critical dynamics is intrinsically linked to the nonuniform bond distribution, being shown to arise from a kinetic coefficient which vanishes with a nonuniversal critical exponent. Nonuniversality of the dynamic exponent for Ising systems with inhomogeneous couplings is argued to be specific to zero-temperature critical points.
A restricted dynamics, previously introduced in a kinetic model for relaxation phenomena in linear polymer chains, is used to study the dynamic critical exponent of one-dimensional Ising models. Both an alternating isotopic chain and an alternating-bond chain are considered. In contrast with what occurs for Glauber dynamics, in these two models the dynamic critical exponent turns out to be the same. The alternating isotopic chain with the restricted dynamics is shown to lead to Nagel scaling for temperatures above some critical value. Further support is given relating the Nagel scaling to the existence of multiple (simultaneous) relaxation processes, the dynamics apparently not playing the most important role in determining such scaling.
Recent results concerning non-universality in the dynamical critical behavior of the one-dimensional Ising model, are generalised to several formulations of the Potts model, using arguments based on domain wall motion. By applying real-space renormalisation group methods, the authors also study the dynamical Ising model, with single flips, both for a period distribution of nearest-neighbor exchanges and for the random chain (with nonzero couplings). They show that the critical dynamical exponent is z=1+J M /J m where J M (J m ) is the greatest (smallest) of the exchanges.
Investigates the bicritical dynamics of one-dimensional bond-diluted kinetic Ising models in the percolation limit at criticality. A wide class of single-spin-flip dynamics is applied and domain boundary diffusion arguments are used to identify the dominant processes producing flipping of the ordered finite chain segments constituting the diluted chain. Exact expressions for the rate of flip as a function of length of segment are obtained and are used to derive corresponding expressions for the decay of equilibrium correlations, and of the magnetisation (from a non-equilibrium uniformly magnetised initial state) in the chain. The results are in agreement with those of earlier rigorous calculations restricted to the special case of Glauber dynamics.