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Canadian Journal of Physics

Zero-temperature properties of quantum spin models on the triangular lattice II: the antiferromagnet

Satoshi Fujiki, Donald D. Betts

Published Jan 1, 1987• 25 citations
Publisher

Abstract

The calculation of two- and four-spin correlations of the [Formula: see text] antiferromagnet has been extended to an N = 21 site triangular lattice. By fitting a quadratic in 1/N to the nearest neighbour transverse spin correlations, we have estimated the ground-state energy per bond on the infinite lattice to be E0/3NJ = −0.2716 ± 0.005. The nearest neighbour longitudinal correlation is estimated to be [Formula: see text]. A short-range order parameter, the chirality, is defined and estimated for the infinite lattice. From the N dependence of the three sublattice or helical magnetization, the spin correlation is conjectured to decay algebraically as [Formula: see text].

DOI
10.1139/p87-013

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International Journal of Modern Physics B•Oct 20, 2010•4 citations
The calculation of two- and four-spin correlations of the [Formula: see text] antiferromagnet has been extended to an N = 21 site triangular lattice. By fitting a quadratic in 1/N to the nearest neighbour transverse spin correlations, we have estimated the ground-state energy per bond on the infinite lattice to be E0/3NJ = −0.2716 ± 0.005. The nearest neighbour longitudinal correlation is estimated to be [Formula: see text]. A short-range order parameter, the chirality, is defined and estimated for the infinite lattice. From the N dependence of the three sublattice or helical magnetization, the spin correlation is conjectured to decay algebraically as [Formula: see text].
The calculation of two- and four-spin correlations of the [Formula: see text] ferromagnet has been extended to an N = 21 site triangular lattice. By fitting a quadratic in 1/N to the nearest neighbour transverse pair correlations, we have estimated the ground-state energy per bond on the infinite lattice to be E0/3NJ = −0.5326 ± 0.003. We conjecture that the square of the magnetization per site vanishes very sharply as N−0.06. The nearest neighbour longitudinal correlation per bond [Formula: see text] for all two-dimensional lattices.
After decades of debate, now there is a rough consensus that at zero temperature the spin-1/21/21/2 Heisenberg antiferromagnet on the triangular lattice is three-sublattice ${120}^{\ensuremath{\circ}}$ magnetically ordered, in contrast to a quantum spin liquid as originally proposed. However, there remains considerable discrepancy in the magnetization reported among various methods. To resolve this issue, in this work we revisit this model by the tensor-network state algorithm. The ground-state energy per bond Eb{E}_{b}Eb​ and magnetization per spin M0{M}_{0}M0​ in the thermodynamic limit are obtained with high precision. The former is estimated to be ${E}_{b}=\ensuremath{-}0.18334(10)$. This value agrees well with that from the series expansion. The three-sublattice magnetic order is firmly confirmed and the magnetization is determined as M0=0.161(5){M}_{0}=0.161(5)M0​=0.161(5). It is about 3232%32 of its classical value and slightly below the lower bound from the series expansion. In comparison with the best estimated value by Monte Carlo and density-matrix renormalization group, our result is about 2020%20 smaller. This magnetic order is consistent with further analysis of the three-body correlation. Our work thus provides benchmark results for this prototypical model.
A Pfaffian representation, of the partition function of the triangular lattice is used to derive expressions for various two, four, and six spin correlations in terms of Pfaffians. The pair correlations along a diagonal are expressed as a Toeplitz determinant whose limiting form yields the spontaneous magnetization. At the ferromagnetic critical point the correlations decay as 1/r12 with approximately radial symmetry. At the antiferromagnetic zero point the ground state is highly degenerate—it has finite entropy—and on a given sublattice the pair correlations along a row decay as ε/r12, where ε=+ε0 on the sublattice containing the origin spin and ε≃−12ε0 on the other two sublattices. Finally, the perpendicular susceptibility, χ⊥, which depends on a finite number of correlations, is calculated; its ferromagnetic behavior is similar to that of the perpendicular susceptibilities of the quadratic and honeycomb lattices, but for an antiferromagnet χ⊥ diverges as 1/T at low temperatures.
We study the spin-1/2 and spin-1 [Formula: see text] Heisenberg antiferromagnets (HAFs) on an infinite, anisotropic, two-dimensional triangular lattice, using the coupled cluster method. With respect to an underlying square-lattice geometry the model contains antiferromagnetic (J1 > 0) bonds between nearest neighbours and competing [Formula: see text] bonds between next-nearest-neighbours across only one of the diagonals of each square plaquette, the same diagonal in each square. In a topologically equivalent triangular-lattice geometry the model has two sorts of nearest-neighbour bonds, with [Formula: see text] bonds along parallel chains and with J1 bonds providing an interchain coupling. The model thus interpolates between an isotropic HAF on the square lattice at one extreme (κ = 0) and a set of decoupled chains at the other (κ → ∞), with the isotropic HAF on the triangular lattice in between at κ = 1. For the spin-1/2 [Formula: see text] model, we find a weakly first-order (or possibly second-order) quantum phase transition from a Néel-ordered state to a helical state at a first critical point at κc1 = 0.80 ± 0.01, and a second critical point at κc2 = 1.8 ± 0.4 where a first-order transition occurs between the helical state and a collinear stripe-ordered state. For the corresponding spin-1 model we find an analogous transition of the second-order type at κc1 = 0.62 ± 0.01 between states with Néel and helical ordering, but we find no evidence of a further transition in this case to a stripe-ordered phase.