Thermodynamics of the frustrated J1J_1-J2J_2 Heisenberg ferromagnet on the body-centered cubic lattice with arbitrary spin

We use the spin-rotation-invariant Green's function method as well as the high-temperature expansion to discuss the thermodynamic properties of the frustrated spin-$S$ $J_{1}$-$J_{2}$ Heisenberg magnet on the body-centered cubic lattice. We consider ferromagnetic nearest-neighbor bonds $J_1 < 0$ and antiferromagnetic next-nearest-neighbor bonds $J_2 \ge 0$ and arbitrary spin $S$. We find that the transition point $J_2^c$ between the ferromagnetic ground state and the antiferromagnetic one is nearly independent of the spin $S$, i.e., it is very close to the classical transition point $J_2^{c,{\rm clas}}= \frac{2}{3}|J_1|$. At finite temperatures we focus on the parameter regime $J_2<J_2^c$ with a ferromagnetic ground-state. We calculate the Curie temperature $T_{C}(S,J_{2})$ and derive an empirical formula describing the influence of the frustration parameter $J_{2}$ and spin $S$ on $T_C$. We find that the Curie temperature monotonically decreases with increasing frustration $J_2$, where very close to $J_2^{c,{\rm clas}}$ the $T_C(J_2)$-curve exhibits a fast decay which is well described by a logarithmic term $1/\textrm{log}(\frac{2}{3}|J_1|-J_{2})$. To characterize the magnetic ordering below and above $T_C$, we calculate the spin-spin correlation functions $\langle {\bf S}_{\bf 0} {\bf S}_{\bf R} \rangle$, the spontaneous magnetization, the uniform static susceptibility $\chi_0$ as well as the correlation length $\xi$. Moreover, we discuss the specific heat $C_V$ and the temperature dependence of the excitation spectrum. As approaching the transition point $J_2^c$ some unusual features were found, such as negative spin-spin correlations at temperatures above $T_C$ even though the ground state is ferromagnetic or an increase of the spin stiffness with growing temperature.Comment: 19 pages, 10 figures, version as in EPJ

Transport coefficients of multi-particle collision algorithms with velocity-dependent collision rules

Detailed calculations of the transport coefficients of a recently introduced particle-based model for fluid dynamics with a non-ideal equation of state are presented. Excluded volume interactions are modeled by means of biased stochastic multiparticle collisions which depend on the local velocities and densities. Momentum and energy are exactly conserved locally. A general scheme to derive transport coefficients for such biased, velocity dependent collision rules is developed. Analytic expressions for the self-diffusion coefficient and the shear viscosity are obtained, and very good agreement is found with numerical results at small and large mean free paths. The viscosity turns out to be proportional to the square root of temperature, as in a real gas. In addition, the theoretical framework is applied to a two-component version of the model, and expressions for the viscosity and the difference in diffusion of the two species are given.Comment: 31 pages, 8 figures, accepted by J. Phys. Cond. Matte

Mesoscopic model for the fluctuating hydrodynamics of binary and ternary mixtures

A recently introduced particle-based model for fluid dynamics with continuous velocities is generalized to model immiscible binary mixtures. Excluded volume interactions between the two components are modeled by stochastic multiparticle collisions which depend on the local velocities and densities. Momentum and energy are conserved locally, and entropically driven phase separation occurs for high collision rates. An explicit expression for the equation of state is derived, and the concentration dependence of the bulk free energy is shown to be the same as that of the Widom-Rowlinson model. Analytic results for the phase diagram are in excellent agreement with simulation data. Results for the line tension obtained from the analysis of the capillary wave spectrum of a droplet agree with measurements based on the Laplace's equation. The introduction of "amphiphilic" dimers makes it possible to model the phase behavior and dynamics of ternary surfactant mixtures.Comment: 7 pages including 6 figure

Effective t-J Hamiltonian for the Copper Oxides

Starting from the Emery model, which is assumed to describe the copper oxygen planes, and including direct oxygen hopping matrix elements, we have been able to derive the effective t-J Hamiltonian for the copper orbitals using the Linked Cluster Expansion Method up to fourth order in the hybridization matrix element.Comment: (ps version of the dvi file, resubmitted because previous uucompressed version was corrupted), 9 page

Consistent particle-based algorithm with a non-ideal equation of state

A thermodynamically consistent particle-based model for fluid dynamics with continuous velocities and a non-ideal equation of state is presented. Excluded volume interactions are modeled by means of biased stochastic multiparticle collisions which depend on the local velocities and densities. Momentum and energy are exactly conserved locally. The equation of state is derived and compared to independent measurements of the pressure. Results for the kinematic shear viscosity and self-diffusion constants are presented. A caging and order/disorder transition is observed at high densities and large collision frequency.Comment: 7 pages including 4 figure

Dynamic correlations in stochastic rotation dynamics

The dynamic structure factor, vorticity and entropy density dynamic correlation functions are measured for Stochastic Rotation Dynamics (SRD), a particle based algorithm for fluctuating fluids. This allows us to obtain unbiased values for the longitudinal transport coefficients such as thermal diffusivity and bulk viscosity. The results are in good agreement with earlier numerical and theoretical results, and it is shown for the first time that the bulk viscosity is indeed zero for this algorithm. In addition, corrections to the self-diffusion coefficient and shear viscosity arising from the breakdown of the molecular chaos approximation at small mean free paths are analyzed. In addition to deriving the form of the leading correlation corrections to these transport coefficients, the probabilities that two and three particles remain collision partners for consecutive time steps are derived analytically in the limit of small mean free path. The results of this paper verify that we have an excellent understanding of the SRD algorithm at the kinetic level and that analytic expressions for the transport coefficients derived elsewhere do indeed provide a very accurate description of the SRD fluid.Comment: 33 pages including 16 figure