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Thermodynamics of the 2D-Heisenberg classical square lattice: Zero-field partition function

Jacques Curély

Published Jan 1, 1998• 0 citations
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In this part labelled I we rigorously examine 2D square lattices composed of (2N+1)2classical spins isotropically coupled between first-nearest neighbors (i.e., showing Heisenberg cou-plings). Each local operator exp(-β Hi,jex) - where Hi,jexis the local exchange Hamiltonian associated with each site (i,j) - is expanded on the basis of spherical harmonics, each one being characterized by the couple of integers (ℓ,m), with ℓ≥0 and m∈[-ℓ,+ℓ]. Using spin lattice symmetries, we derive selection rules over these coefficients, thus allowing to express the zero-field partition function ZN(0). In the thermodynamic limit (N→∞), we show that the value m=0 is selected while ℓ=ℓ0≥0, ∀(i,j). A very simple closed-form expression may be then derived for ZN(0). Finally we report a thermal study of the current term of the characteristic polynomial giving ZN(0). We show that it appears crossovers between two consecutive terms characterized by integers ℓ and ℓ+1, respectively. Coming from high temperatures where the term characterized by ℓ=0 is dominant, near absolute zero, increasing ℓ-values are more and more selected when the temperature is cooling down. But, when T reaches zero, all the successive dominant terms become equivalent and are characterized by the value ℓ=0. We show that this property also prevails at T=0 K rigorously. This confirms the fact that, for a 2D lattice showing Heisenberg couplings, the critical temperature is TC=0 K, in agreement with Mermin-Wagner's theorem.

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In this part labelled I we rigorously examine 2D square lattices composed of (2N+1)2classical spins isotropically coupled between first-nearest neighbors (i.e., showing Heisenberg cou-plings). Each local operator exp(-β Hi,jex) - where Hi,jexis the local exchange Hamiltonian associated with each site (i,j) - is expanded on the basis of spherical harmonics, each one being characterized by the couple of integers (ℓ,m), with ℓ≥0 and m∈[-ℓ,+ℓ]. Using spin lattice symmetries, we derive selection rules over these coefficients, thus allowing to express the zero-field partition function ZN(0). In the thermodynamic limit (N→∞), we show that the value m=0 is selected while ℓ=ℓ0≥0, ∀(i,j). A very simple closed-form expression may be then derived for ZN(0). Finally we report a thermal study of the current term of the characteristic polynomial giving ZN(0). We show that it appears crossovers between two consecutive terms characterized by integers ℓ and ℓ+1, respectively. Coming from high temperatures where the term characterized by ℓ=0 is dominant, near absolute zero, increasing ℓ-values are more and more selected when the temperature is cooling down. But, when T reaches zero, all the successive dominant terms become equivalent and are characterized by the value ℓ=0. We show that this property also prevails at T=0 K rigorously. This confirms the fact that, for a 2D lattice showing Heisenberg couplings, the critical temperature is TC=0 K, in agreement with Mermin-Wagner's theorem.
We start this article by recalling rigorous results previously obtained for 2d square lattices composed of (2N+1)2classical spins isotropically coupled between first-nearest neighbors (i.e., showing Heisenberg couplings), in the thermodynamic limit (N→+∞) [4]: (i) the zero-field partition function ZN(0), (ii) the spin correlation which vanishes in the zero-field limit, except at T=0 K so that the critical temperature is TC=0 K, in agreement with Mermin-Wagner's theorem, (iii) the spin-spin correlation between any two lattice sites, (iv) the correlation length and (v) the static susceptibility. We exclusively focus on the low-temperature behaviors of the correlation length and the static susceptibility. This leads to the determination of a diagram characterized by three magnetic phases. Moreover we show that all the behaviors are in perfect agreement with the corresponding ones derived by using a renormalization method. Finally we give criterions allowing to directly determine the magnetic phases characterizing 2d magnetic compounds described by our microscopic model. An experimental test is given for illustrating this theoretical study.