Abstract
The Schrödinger exchange interaction for arbitrary spin is used to construct a Hamiltonian for a nearest-neighbor model of ferromagnetism. The general high-temperature series for the low-field susceptibility is developed, and the first three terms of the series, for arbitrary crystal lattices, are calculated. The Curie temperature obtained from setting χ1=0 and taking the first two terms (molecular-field theory) or three terms ("Heisenberg Gaussian" approximation), is given by (2S+1)kBTCJ=z or 4[1(18z)12], respectively. The functional dependence on z (number of nearest neighbors) of the latter result, for arbitrary S, is exactly the same as originally obtained by Heisenberg for S=12. In general, the exchange model appears to disorder at a lower temperature than the Heisenberg model, as could be anticipated from the higher degeneracy of the ground state of a pair of spins interacting with the exchange Hamiltonian compared to the Heisenberg Hamiltonian.