The method of the two-time temperature-dependent Green's function has been used to analyze the Ising model of a ferromagnet in an external magnetic field. The selection of a particular Green's function enables us to write an exact expression for the equation of motion. We are then led to a differential difference equation for the correlation function corresponding to the Green's function. No decoupling assumptions have been made, so the equation is exact for both arbitrary spin and range of interaction. It is shown how various approximate theories may be extracted from our formalism. The exact differential difference equation may be reduced to a partial differential equation. The latter form allows us to generate relations among the magnetization and spin-spin correlation functions. These relations are given in detail for the case of spin \textonehalf{} and $z$ nearest neighbors.
The method of the two-time temperature-dependent Green's function has been used to analyze the Ising model of a ferromagnet in an external magnetic field. The selection of a particular Green's function enables us to write an exact expression for the equation of motion. We are then led to a differential difference equation for the correlation function corresponding to the Green's function. No decoupling assumptions have been made, so the equation is exact for both arbitrary spin and range of interaction. It is shown how various approximate theories may be extracted from our formalism. The exact differential difference equation may be reduced to a partial differential equation. The latter form allows us to generate relations among the magnetization and spin-spin correlation functions. These relations are given in detail for the case of spin \textonehalf{} and z nearest neighbors.
In the usual theory of the two-time Green's function, decoupling techniques are introduced in order to obtain a self-closed equation for the lowest order Green's function. These decouplings give neither the correct temperature dependence (the absence of a T3 term) of magnetization nor the correct correlation function $〈{{S}_{j}}^{\ensuremath{-}}{{S}_{j}}^{\ensuremath{-}}{{S}_{k}}^{+}{{S}_{l}}^{+}〉$, which should be zero by definition. In this paper the equation of motion for the higher order Green's function is solved in the approximation which will lead to correct results up to terms of order T3 in these quantities. Employing this higher order Green's function, it is found that the correction to the magnetization consists of a term of order T4 and a divergent term and that the correlation function consists of a term of order T3 and a divergent term. A method extracting a significant part from this divergent term is found by analyzing a system of two interacting \textonehalf{} spins. By this method, it is shown that the T3 term in the magnetization is completely eliminated and that the correlation function $〈{{S}_{j}}^{\ensuremath{-}}{{S}_{j}}^{\ensuremath{-}}{{S}_{k}}^{+}{{S}_{l}}^{+}〉$ vanishes identically.
The Green function method is applied to the Ising model of ferromagnetism. It is essential in this paper that we have solved the equations for the Green functions in terms of the correlation functions without using the approximation of decoupling the Green functions as is usually done. Although we get several rigorous relations between the many-spin correlation functions, we do not succeed in solving for the correlation functions, except in the case of a linear chain. We introduce the approximation of eliminating some of the correlation functions using the high temperature expansion, so as to reduce the number of the independent correlation functions. The Curie points of a square lattice and a simple cubic lattice are calculated.
In this paper we present Green function technique applied to calculations of spin-spin correlations in systems governed by Ising Hamiltonian. This offers approximate yet reasonably accurate analytical results, as an alternative approach to direct computer simulation. Local spin operators are represented in terms of particle operators for fermions. Chain of Green functions for local magnetization on given site involves nearest neighbors and it is decoupled at the next-nearest-neighbors level. Therefore, still accounts at the lowest level for magnetic correlations between nearest neighbors. This technique was applied to binary alloy A x B 1-x with given atomic short range order. Calculations for stoichiometric x=1/2 composition show how temperature dependence of magnetization and spin-spin correlations are modified when atomic order parameter changes. We scanned this parameter from the case of ordered binary alloy, via random alloy, to clusterlike structure. In model calculations we (a) confirm characteristic λ -like shape of the magnetic specific heat near Curie temperature and (b) recover essential results of exact, two-dimensional Ising model. This supports our claim of usefulness of such analytical approach, which is easy and flexible to describe different geometries (clusters, thin films) and conditions imposed on spins located on specific atoms (spins partly pinned on the surface atoms).
We exactly solve the ferromagnetic spin- 1/2 Ising model on the Bethe lattice in the presence of an external magnetic field by means of the equations of motion method within the Green's function formalism. In particular, such an approach is applied to an isomorphic model of localized Fermi particles interacting via an intersite Coulomb interaction. A complete set of eigenoperators is found together with the corresponding eigenvalues. The Green's functions and the correlation functions are written in terms of a finite set of parameters to be self-consistently determined. A procedure is developed that allows us to exactly fix the unknown parameters in the case of a Bethe lattice with any coordination number z. Nonlocal correlation functions up to four points are also provided together with a study of the relevant thermodynamic quantities.
The one-dimensional Heisenberg model with S = 1/2 is treated with the use of the two-time Green's functions. The hierarchy of the equations of motion of the Green'f functions is decoupled at a stage one-step further than Tyablikov's decoupling. The thermal average of the spin component, ≪ Sz >, is set to zero, becaure the long-range order does not exist in one dimension. Instead, our Green's functions are expressed in terms of the correlation functions cn ≡4≪ S0zSnz >. The Green's function is essentially of the form representing undamped spin waves, whose spactrum depends on c1, c2 and one more parameter. They are determined by the requirement that c1 and c2 should be self-consistent and that c0 should be unity. The self-consistency equations have been solved analytically at high- and low-temperature limits, and also solved numerically in the whole range of the temperature. Thermodynamic quantities have been calculated using these solutions. It has turned out that the theory gives the correct high-temperature expansion for the thermodynamic quantities and the correlation functions. The latter is expressed by cn = (J / 4 kBT )n. In the case of ferromagnetic coupling, the correlation function cn at T = 0 is equal to 1/3 for all n's. This is what is expected from the correct ground state of the ferromagnetic Heisenberg system. The spin-wave spectrum at T = 0 also agrees with the correct one. At T ≪J/ kB, we find that the specific heat goes as T1/2 and the susceptibility goes as T-2. The gross feature of the temperature-dependence of the thermodynamic quantities agrees with Bonner and Fisher. In the case of the antiferromagnetic Heisenberg model, we find c1 = -0.55407 and c2 = 0.16100 at T = 0, which are fairly close to the exact values. The thermodynamic quantities are also in gross agreement with Bonner and Fisher.
A statistical theory of the localized model of ferromagnetism is developed by considering the effective density matrices for a single spin, and two nearest-neighbor spins, respectively. The Ising Model and the Heisenberg model, and even the case of the anisotropic exchange interaction, are treated within a unified mathematical scheme. The result is reduced to that of the Bethe approximation in the case of the Ising model, and the constant coupling approximation in the case of the Heisenberg model. The method is generalized to calculate the static spin-correlation function. It is obtained in Ornstein-Zernike type. In the nonequilibrium state, the expectation value of the spin decays by the homogeneous damping as well as the spin-diffusion process. This relaxation equation is different from that by Van Hove because of the existence of the homogeneous damping. The diffusion constant does not vanish even at the Curie point TC, contrary to Van Hove's result, although the damping constant vanishes at TC. The latter fact causes the critical slowing down of the regression of fluctuation. The solution of this relaxation equation gives the time-dependent spin-correlation function. The method can be applied to the antiferromagnetic case, too.