Non-universal dynamics is shown to occur in a one-dimensional non-equilibrium system of hard-core particles. The stochastic processes included are pair creation and annihilation (with rates and ) and symmetric hopping rates which alternate from one bond to the next ( , ). A dynamical scaling relation between the relaxation time and the correlation length in the steady state is derived in a simple way for the case . We find that the dynamical exponent takes the non-universal value . For the special condition , where the stochastic system is in principle soluble by reduction to a free fermion system, the model is mapped to the Glauber dynamics of an Ising chain with alternating ferromagnetic bonds of values and , in contact with a quantum thermal bath. The full time dependence of the space-dependent magnetization and of the equal time spin-spin correlation function are studied by writing the master equation for this system in the quantum Hamiltonian formalism. In particular, we obtain the dispersion relations and rigorously confirm the results obtained for the correlation length and for the dynamical exponent.
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.
We show that the stochastic dynamics of a large class of one-dimensional interacting particle systems may be presented by integrable quantum spin Hamiltonians. Generalizing earlier work [1, 2] we present an alternative description of these processes in terms of a time-dependent operator algebra with quadratic relations. These relations generate the Bethe ansatz equations for the spectrum and turn the calculation of time-dependent expectation values into the problem of either finding representations of this algebra or of solving functional equations for the initial values of the operators. We use both strategies for the study of two specific models: (i) We construct a two-dimensional time-dependent representation of the algebra for the symmetric exclusion process with open boundary conditions. In this way we obtain new results on the dynamics of this system and on the eigenvectors and eigenvalues of the corresponding quantum spin chain, which is the isotropic Heisenberg ferromagnet with non-diagonal, symmetry-breaking boundary fields. (ii) We consider the non-equilibrium spin relaxation of Ising spins with zero-temperature Glauber dynamics and an additional coupling to an infinite-temperature heat bath
The equal-time correlation function for an Ising chain with alternating ferromagnetic coupling constants (
J1>
J2) and Glauber dynamics has been calculated. Averaging over random initial conditions shows that the correlation function is independent of the probability distribution for the initial conditions, but depends on the nontrivial combination of different coupling constants, which casts some doubt as to the validity of the scaling form C(r,t)=f(
r2/t). Furthermore, by calculating the spin-spin correlations for different times, we find that the power-law decay of the autocorrelation function has the same scaling form as in the simple uniform case C(0,t,t')\ensuremath{\sim}(2/\ensuremath{\pi})(2t/t'
)1/2, for t'\ensuremath{\gg}t. This may suggest that a different exponent, instead of the dynamic critical exponent z=1+
J1/
J2, is needed to characterize the scaling of the autocorrelation function.
We study the effect of antiferromagnetic interactions on the single spin-flip Glauber dynamics of two different one-dimensional Ising models with spin $\ifmmode\pm\else\textpm\fi{}1$. The first model is an Ising chain with antiferromagnetic exchange interaction limited to nearest neighbors and subject to an oscillating magnetic field. The system of master equations describing the time evolution of sublattice magnetizations can easily be solved within a linear field approximation and a long time limit. Resonant behavior of the magnetization as a function of temperature (stochastic resonance) is found, at low frequency, only when spins on opposite sublattices are uncompensated owing to different gyromagnetic factors (i.e., in the presence of a ferrimagnetic short range order). The second model is the axial next-nearest-neighbor Ising (ANNNI) chain, where an antiferromagnetic exchange between next-nearest neighbors is assumed to compete with a nearest-neighbor exchange interaction of either sign. The long time response of the model to a weak, oscillating magnetic field is investigated in the framework of a decoupling approximation for three-spin correlation functions, which is required to close the system of master equations. The calculation, within such an approximate theoretical scheme, of the dynamic critical exponent
z, defined as $1∕\ensuremath{\tau}\ensuremath{\approx}{(1∕\ensuremath{\xi})}^{z}$ (where $\ensuremath{\tau}$ is the longest relaxation time and $\ensuremath{\xi}$ is the correlation length of the chain), suggests that the
T=0 single spin-flip Glauber dynamics of the ANNNI chain is in a different universality class than that of the unfrustrated Ising chain.
We present the exact solution for the full dynamics of a nonequilibrium spin chain and its dual reaction-diffusion model, for arbitrary initial conditions. The spin chain is driven out of equilibrium by coupling alternating spins to two thermal baths at different temperatures. In the reaction-diffusion model, this translates into spatially alternating rates for particle creation and annihilation, and even negative "temperatures" have a perfectly natural interpretation. Observables of interest include the magnetization, the particle density, and all correlation functions for both models. Two generic types of time dependence are found: if both temperatures are positive, the magnetization, density, and correlation functions decay exponentially to their steady-state values. In contrast, if one of the temperatures is negative, damped oscillations are observed in all quantities. They can be traced to a subtle competition of pair creation and annihilation on the two sublattices. We comment on the limitations of mean-field theory and propose an experimental realization of our model in certain conjugated polymers and linear chain compounds.