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arXiv:cond-mat/0206159 · Physical review. B, Condensed matter

Classical dimers on the triangular lattice

Paul Fendley, Roderich Moessner, Shivaji L. Sondhi

Published Dec 13, 2002• 141 citations

Abstract

We study the classical hard-core dimer model on the triangular lattice. Following Kasteleyn's fundamental theorem on planar graphs, this problem is soluble using Pfaffians. This model is particularly interesting for, unlike the dimer problems on the bipartite square and hexagonal lattices, its correlations are short ranged with a correlation length of less than one lattice constant. We compute the dimer-dimer and monomer-monomer correlators, and find that the model is deconfining: the monomer-monomer correlator falls off exponentially to a constant value $0.1494\dots{},$ only slightly below the nearest-neighbor value of $1/6.$ We also consider the anisotropic triangular lattice model in which the square lattice is perturbed by diagonal bonds of one orientation and small fugacity. We show that the model becomes noncritical immediately and that this perturbation is equivalent to adding a mass term to each of two Majorana fermions that are present in the long wavelength limit of the square lattice problem.

DOI: 10.1103/physrevb.66.214513

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We study the classical hard-core dimer model on the triangular lattice. Following Kasteleyn's fundamental theorem on planar graphs, this problem is soluble using Pfaffians. This model is particularly interesting for, unlike the dimer problems on the bipartite square and hexagonal lattices, its correlations are short ranged with a correlation length of less than one lattice constant. We compute the dimer-dimer and monomer-monomer correlators, and find that the model is deconfining: the monomer-monomer correlator falls off exponentially to a constant value

0.1494\dots{},

only slightly below the nearest-neighbor value of

1/6.

We also consider the anisotropic triangular lattice model in which the square lattice is perturbed by diagonal bonds of one orientation and small fugacity. We show that the model becomes noncritical immediately and that this perturbation is equivalent to adding a mass term to each of two Majorana fermions that are present in the long wavelength limit of the square lattice problem.

We derive exact results for close-packed dimers on the triangular kagome lattice (TKL), formed by inserting triangles into the triangles of the kagome lattice. Because the TKL is a nonbipartite lattice, dimer-dimer correlations are short ranged so that the ground state at the Rokhsar-Kivelson (RK) point of the corresponding quantum dimer model on the same lattice is a short-ranged spin liquid. Using the Pfaffian method, we derive an exact form for the free energy, and we find that the entropy is

\frac{1}{3}\text{ln}\text{ }2

per site, regardless of the weights of the bonds. The occupation probability of every bond is

\frac{1}{4}

in the case of equal weights on every bond. Similar to the case of lattices formed by corner-sharing triangles (such as the kagome and squagome lattices), we find that the dimer-dimer correlation function is identically zero beyond a certain (short) distance. We find in addition that monomers are deconfined on the TKL, indicating that there is a short-ranged spin liquid phase at the RK point. We also find exact results for the ground-state energy of the classical Heisenberg model. The ground state can be ferromagnetic, ferrimagnetic, locally coplanar, or locally canted, depending on the couplings. From the dimer model and the classical spin model, we derive upper bounds on the ground-state energy of the quantum Heisenberg model on the TKL.

We study classical hard-core dimer models on the square lattice with links extending beyond nearest-neighbors. Numerically, using a directed-loop Monte Carlo algorithm, we find that, in the presence of longer dimers preserving the bipartite graph structure, algebraic correlations persist. While the confinement exponent for monomers drifts, the leading decay of dimer correlations remains

1∕{r}^{2}

, although the logarithmic peaks present in the dimer structure factor of the nearest-neighbor model vanish. By contrast, an arbitrarily small fraction of next-nearest-neighbor dimers leads to the onset of exponential dimer correlations and deconfinement. We discuss these results in the framework of effective theories, and provide an approximate but accurate analytical expression for the dimer correlations.

We study the correlations of classical hard-core dimer models doped with monomers by Monte Carlo simulation. We introduce an efficient cluster algorithm, which is applicable in any dimension, for different lattices and arbitrary doping. We use this algorithm for the dimer model on the square lattice, where a finite density of monomers destroys the critical confinement of the two-monomer problem. The monomers form a two-component plasma located in its high-temperature phase, with the Coulomb interaction screened at finite densities. On the triangular lattice, a single pair of monomers is not confined. The monomer correlations are extremely short ranged and hardly change with doping.

We consider a classical interacting dimer model which interpolates between the square lattice case and the triangular lattice case by tuning a chemical potential in the diagonal bonds. The interaction energy simply corresponds to the number of plaquettes with parallel dimers. Using transfer matrix calculations, we find in the anisotropic triangular case a succession of different physical phases as the interaction strength is increased: a short-range disordered liquid dimer phase at low interactions, then a critical phase similar to the one found for the square lattice, and finally a transition to an ordered columnar phase for large interactions. Our results indicate that criticality and nonbipartiteness are compatible in a dimer model. For the isotropic triangular case, we have indications that the system undergoes a first-order phase transition to an ordered phase, without appearance of an intermediate critical phase.

A square-lattice hard-core dimer model with links extending beyond nearest-neighbors is studied using a directed-loop Monte Carlo method. An arbitrarily small fraction of next-nearest-neighbor dimers is found to cause deconfinement, whereas a critical state with

r^{-2}

distance dependence of the dimer-dimer correlations persists in the presence of longer dimers preserving the bipartite graph structure. However, the critical confinement exponent governing the correlation of two test monomers is non-universal. Implications for resonating-valence-bond states are discussed.