The two-dimensional antiferromagnetic S=1/2 Heisenberg model with random bond dilution is studied using quantum Monte Carlo simulation at the percolation threshold (50% of the bonds removed). Finite-size scaling of the staggered structure factor averaged over the largest connected clusters of sites on L*L lattices shows that long-range order exists within the percolating fractal clusters in the thermodynamic limit. This implies that the order-disorder transition driven by bond-dilution occurs exactly at the percolation threshold and that the exponents are classical. This result should apply also to the site-diluted system.
The two-dimensional antiferromagnetic
S=1/2 Heisenberg model with random site dilution is studied using quantum Monte Carlo simulations. Ground-state properties of the largest connected cluster on $L\ifmmode\times\else\texttimes\fi{}L$ lattices, with L up to 64, are calculated at the classical percolation threshold. In addition, clusters with a fixed number
Nc of spins on an infinite lattice at the percolation density are studied for
Nc up to 1024. The disorder averaged sublattice magnetization per spin extrapolates to the same nonzero infinite-size value for both types of clusters. Hence, the percolating clusters, which are fractal with dimensionality
d=91/48, have antiferromagnetic long-range order. This implies that the order-disorder transition driven by site dilution occurs exactly at the percolation threshold and that the exponents are classical. The same conclusion is reached for the bond-diluted system. The full sublattice magnetization versus site dilution curve is obtained in terms of a decomposition into a classical geometrical factor and a factor containing all the effects of quantum fluctuations. The spin stiffness is shown to obey the same scaling as the conductivity of a random resistor network.
We study the phase diagram and the quantum phase transitions of a site-diluted two-dimensional O(3) quantum rotor model by means of large-scale Monte Carlo simulations. This system has two quantum phase transitions: a generic one for small dilutions and a percolation transition across the lattice percolation threshold. We determine the critical behavior for both transitions and for the multicritical point that separates them. In contrast to the exotic scaling scenarios found in other random quantum systems, all these transitions are characterized by finite-disorder fixed points with power-law scaling. We relate our findings to a recent classification of phase transitions with quenched disorder according to the rare region dimensionality, and we discuss experiments in disordered quantum magnets.
We study the low-energy dynamics of
S=1/2 antiferromagnetic Heisenberg clusters constructed by diluting a square lattice at vacancy concentration
p at and below the percolation threshold ${p}^{\ensuremath{\ast}}\ensuremath{\approx}0.407$. The finite-size scaling behavior of the average excitation gap, $⟨\ensuremath{\Delta}⟩\ensuremath{\sim}{L}^{\ensuremath{-}z}$, where
L is the cluster length, is obtained using quantum Monte Carlo results for an upper bound ${\ensuremath{\Delta}}^{\ensuremath{\ast}}$ to $\ensuremath{\Delta}$, derived from sum rules. At the percolation threshold, we obtain a dynamic exponent $z=3.6\ifmmode\pm\else\textpm\fi{}0.1\ensuremath{\approx}2{D}_{f}$ for clusters with singlet
(S=0) ground state. Here
Df=91/48 is the fractal dimensionality of the percolating cluster. We argue that this large dynamic exponent---roughly twice that expected for quantum-rotor excitations---is a consequence of weakly interacting localized effective magnetic moments, which form due to local sublattice imbalance. This picture is supported by an extremal-value analysis of local spectral gaps, which delivers an exponent relation (between
z and two exponents characterizing the local-gap distribution) reproduced by our simulation data. However, the average $⟨{\ensuremath{\Delta}}^{\ensuremath{\ast}}⟩$ over all clusters, which have mostly ground-state spin
S>0, scales with a smaller exponent than for the
S=0 clusters alone; $z\ensuremath{\approx}1.5{D}_{f}$. Lanczos exact diagonalization for small clusters show that typically, $S\ensuremath{\rightarrow}S\ensuremath{-}1$ in the lowest-energy excitations while the dominant spectral weight originates from $S\ensuremath{\rightarrow}S+1$ excitations. Thus, the scaling of $⟨{\ensuremath{\Delta}}^{\ensuremath{\ast}}⟩$ for clusters with ground state
S>0 does not reflect the lowest-energy excitations but the higher $S\ensuremath{\rightarrow}S+1$ excitations. This result can be understood within a valence bond picture. To further explore the scenario of localized moments, we introduce a classical dimer-monomer aggregation model to study the distribution of nearest-neighbor sites forming dimers (which are the objects used in mapping to the quantum-rotor model) and unpaired spins (monomers). The monomers are localized and, thus, effective magnetic moments should form in the spin system. We also study the lowest triplet excitation of
S=0 clusters using quantum Monte Carlo calculations in the valence bond basis. The triplet is concentrated at some of the classical monomer regions, confirming the mechanism of moment formation. The number of spins (and moment regions) affected by the excitation scales as a nontrivial power of the cluster size. For a dimer-diluted bilayer Heisenberg model with weak interlayer coupling (where the system remains N\'eel ordered), there is no sublattice imbalance. In this case we find $z\ensuremath{\approx}{D}_{f}$, consistent with quantum-rotor excitations. For a single layer at $p<{p}^{\ensuremath{\ast}}$ we find $z\ensuremath{\approx}2=D$, which indicates that the weakly interacting localized moment mechanism is valid only exactly at the percolation point. There is a crossover behavior close to the percolation point.
The critical spin-wave dynamics of dilute ferromagnetic and antiferromagnetic Heisenberg systems near the percolation threshold is studied on a two-dimensional regular (fractal) model for bond percolation, which captures the relevant geometric features of the cluster structure. The dynamic critical exponent and spectral dimension for both the ferromagnetic and antiferromagnetic systems are calculated. The treatment of the dynamics in these systems requires the use of generalised scaling techniques for sublattice systems, which involve an extension of the parameter space.
We investigate quantum phase transitions in the spin-
1∕2 Heisenberg antiferromagnet on square lattices with inhomogeneous bond dilution. It is shown that quantum fluctuations can be continuously tuned by inhomogeneous bond dilution, eventually leading to the destruction of long-range magnetic order on the percolating cluster. Two multicritical points are identified at which the magnetic transition separates from the percolation transition, introducing a quantum phase transition. Beyond these multicritical points a quantum-disordered phase appears, characterized by an infinite percolating cluster with short ranged antiferromagnetic order. In this phase, the low-temperature uniform susceptibility diverges algebraically with non-universal exponents. This is a signature that the quantum-disordered phase is a quantum Griffiths phase, as also directly confirmed by the statistical distribution of local gaps. This study thus presents evidence of a genuine quantum Griffiths phenomenon in a two-dimensional Heisenberg antiferromagnet.