Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:1703.04223 · Physical review. B./Physical review. B

Dynamic scaling of the restoration of rotational symmetry in Heisenberg quantum antiferromagnets

Phillip Weinberg, Anders W. Sandvik

Published Aug 28, 2017• 6 citations
arXivHTMLPDF

Abstract

We apply imaginary-time evolution with the operator ${e}^{\ensuremath{-}\ensuremath{\tau}H}$ to study relaxation dynamics of gapless quantum antiferromagnets described by the spin-rotation-invariant Heisenberg Hamiltonian $H$. Using quantum Monte Carlo simulations to obtain unbiased results, we propagate an initial state with maximal order parameter ${m}_{s}^{z}$ (the staggered magnetization) in the $z$ spin direction and monitor the expectation value $\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}$ as a function of imaginary time $\ensuremath{\tau}$. Results for different system sizes (lengths) $L$ exhibit an initial essentially size independent relaxation of $\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}$ toward its value in the infinite-size spontaneously symmetry broken state, followed by a strongly size dependent final decay to zero when the $\mathrm{O}(3)$ rotational symmetry of the order parameter is restored. We develop a generic finite-size scaling theory that shows the relaxation time diverges asymptotically as ${L}^{z}$, where $z$ is the dynamic exponent of the low-energy excitations. We use the scaling theory to develop a practical way of extracting the dynamic exponent from the numerical finite-size data, systematically eliminating scaling corrections. We apply the method to spin-$1/2$ Heisenberg antiferromagnets on two different lattice geometries: the standard two-dimensional (2D) square lattice and a site-diluted 2D square lattice at the percolation threshold. In the 2D case we obtain $z=2.001(5)$, which is consistent with the known value $z=2$, while for the site-diluted lattice we find $z=3.90(1)$ or $z=2.056(8){D}_{f}$, where ${D}_{f}=91/48$ is the fractal dimensionality of the percolating system. This is an improvement on previous estimates of $z\ensuremath{\approx}3.7$. The scaling results also show a fundamental difference between the two cases; for the 2D square lattice, the data can be collapsed onto a common scaling function even when $\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}$ is relatively large, reflecting the Anderson tower of quantum rotor states with a common dynamic exponent $z=2$. For the diluted 2D square lattice, the scaling works well only for small $\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}$, indicating a mixture of different relaxation-time scalings between the low-energy states. Nevertheless, the low-energy dynamic here also corresponds to a tower of excitations.

DOI
10.1103/physrevb.96.054442

Related papers

Low-energy excitations of two-dimensional diluted Heisenberg quantum antiferromagnets

Ling Wang, Anders W. Sandvik

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 ${D}_{f}=91/48$ 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.

arXiv:0909.5211•Physical Review B•Feb 16, 2010•32 citations

Low-Energy Dynamics of the Two-Dimensional S = 1 / 2 Heisenberg Antiferromagnet on Percolating Clusters

Ling Wang, Anders W. Sandvik

We investigate the quantum dynamics of site diluted S=1/2 Heisenberg antiferromagnetic clusters at the 2D percolation threshold. We use Lanczos diagonalization to calculate the lowest excitation gap Delta and, to reach larger sizes, use quantum Monte Carlo simulations to study an upper bound for Delta obtained from sum rules involving the staggered structure factor and susceptibility. Scaling the gap distribution with the cluster length L, Delta approximately L(-), we obtain a dynamic exponent z approximately 2D(f), where D(f)=91/48 is the fractal dimensionality of the percolating cluster. This is in contrast with previous expectations of z=D(f). We argue that the low-energy excitations are due to weakly coupled effective moments formed due to local imbalance in sublattice occupation.

arXiv:cond-mat/0606159•Physical Review Letters•Sep 15, 2006•24 citations

Quantum Phase Transition of Two-Dimensional Diluted Heisenberg Antiferromagnet

Synge Todo, Chitoshi Yasuda, Kiyoshi Katō +4 more

Quantum phase transition of site-diluted and bond-diluted Heisenberg antiferromagnets on square lattices is studied. By using the novel continuous-time loop algorithm, we perform quantum Monte Carlo simulations on quite larger lattices at extremely lower temperatures than the previous numerical studies. It is found that the antiferromagnetic long-range order at T = 0 persists so long as a cluster of magnetic sites percolates, that is, the critical concentration is equal to the classical percolation threshold, in both of the site-diluted and bond-diluted cases. Furthermore, we find that some critical exponents, such as the magnetization exponent β, are non-classical and strongly depend on the spin size S. On the other hand, we show that the correlation-length exponent ν is universal and is equal to the classical value (ν=4/3).

Progress of Theoretical Physics Supplement•Jan 1, 2000•2 citations

QUANTUM MONTE CARLO STUDY OF SITE-DILUTED HEISENBERG ANTIFERROMAGNET ON A SQUARE LATTICE

Synge Todo, Kiyoshi Katō, Hajime Takayama +3 more

Ground-state phase transition of site-diluted Heisenberg antiferromagnets on a square lattice is studied. By using the continuous-time loop algorithm, we perform large-scale quantum Monte Carlo simulation on large systems at quite low temperatures. It is found that the critical concentration of magnetic sites is independent of the spin size S, and equal to the classical percolation threshold. However, the existence of quantum fluctuations makes the critical exponents deviate from those of the classical percolation transition. It is found that the transition is not universal, i.e., the critical exponents depend on the spin size S.

International Journal of Modern Physics C•Dec 1, 1999•1 citation

Finite-size scaling of the ground-state parameters of the two-dimensional Heisenberg model

Anders W. Sandvik

The ground-state parameters of the two-dimensional $S=1/2$ antiferromagnetic Heisenberg model are calculated using the stochastic series expansion quantum Monte Carlo method for $L\ifmmode\times\else\texttimes\fi{}L$ lattices with $L$ up to $16$. The finite-size results for the energy $E$, the sublattice magnetization $M$, the long-wavelength susceptibility ${\ensuremath{\chi}}_{\ensuremath{\perp}}(q=2\ensuremath{\pi}/L)$, and the spin stiffness ${\ensuremath{\rho}}_{s},$ are extrapolated to the thermodynamic limit using fits to polynomials in $1/L$, constrained by scaling forms previously obtained from renormalization-group calculations for the nonlinear $\ensuremath{\sigma}$ model and chiral perturbation theory. The results are fully consistent with the predicted leading finite-size corrections, and are of sufficient accuracy for extracting also subleading terms. The subleading energy correction $(\ensuremath{\sim}{1/L}^{4})$ agrees with chiral perturbation theory to within a statistical error of a few percent, thus providing numerical confirmation of the finite-size scaling forms to this order. The extrapolated ground- state energy per spin is $E=\ensuremath{-}0.669437(5)$. The result from previous Green's function Monte Carlo (GFMC) calculations is slightly higher than this value, most likely due to a small systematic error originating from ``population control'' bias in GFMC. The other extrapolated parameters are $M=0.3070(3)$, ${\ensuremath{\rho}}_{s}=0.175(2)$, ${\ensuremath{\chi}}_{\ensuremath{\perp}}=0.0625(9)$, and the spin-wave velocity $c=1.673(7)$. The statistical errors are comparable with those of previous estimates obtained by fitting loop algorithm quantum Monte Carlo data to finite-temperature scaling forms. Both $M$ and ${\ensuremath{\rho}}_{s}$ obtained from the finite-$T$ data are, however, a few error bars higher than the present estimates. It is argued that the $T=0$ extrapolations performed here are less sensitive to effects of neglected higher-order corrections, and therefore should be more reliable.

arXiv:cond-mat/9707123•Physical review. B, Condensed matter•Nov 1, 1997•490 citations

Quantum Phase Transition of the Randomly Diluted Heisenberg Antiferromagnet on a Square Lattice

Kiyoshi Katō, Synge Todo, Kenji Harada +3 more

Ground-state magnetic properties of the diluted Heisenberg antiferromagnet on a square lattice are investigated by means of the quantum Monte Carlo method with the continuous-time loop algorithm. It is found that the critical concentration of magnetic sites is independent of the spin size S, and equal to the two-dimensional percolation threshold. However, the existence of quantum fluctuations makes the critical exponents deviate from those of the classical percolation transition. Furthermore, we found that the transition is not universal, i.e., the critical exponents significantly depend on S.

arXiv:cond-mat/9905379•Physical Review Letters•May 1, 2000•68 citations
We apply imaginary-time evolution with the operator e\ensuremath−\ensuremathτH{e}^{\ensuremath{-}\ensuremath{\tau}H}e\ensuremath−\ensuremathτH to study relaxation dynamics of gapless quantum antiferromagnets described by the spin-rotation-invariant Heisenberg Hamiltonian HHH. Using quantum Monte Carlo simulations to obtain unbiased results, we propagate an initial state with maximal order parameter msz{m}_{s}^{z}msz​ (the staggered magnetization) in the zzz spin direction and monitor the expectation value \ensuremath⟨ms\ensuremath⟩\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}\ensuremath⟨ms​\ensuremath⟩ as a function of imaginary time \ensuremathτ\ensuremath{\tau}\ensuremathτ. Results for different system sizes (lengths) LLL exhibit an initial essentially size independent relaxation of \ensuremath⟨ms\ensuremath⟩\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}\ensuremath⟨ms​\ensuremath⟩ toward its value in the infinite-size spontaneously symmetry broken state, followed by a strongly size dependent final decay to zero when the O(3)\mathrm{O}(3)O(3) rotational symmetry of the order parameter is restored. We develop a generic finite-size scaling theory that shows the relaxation time diverges asymptotically as Lz{L}^{z}Lz, where zzz is the dynamic exponent of the low-energy excitations. We use the scaling theory to develop a practical way of extracting the dynamic exponent from the numerical finite-size data, systematically eliminating scaling corrections. We apply the method to spin-1/21/21/2 Heisenberg antiferromagnets on two different lattice geometries: the standard two-dimensional (2D) square lattice and a site-diluted 2D square lattice at the percolation threshold. In the 2D case we obtain z=2.001(5)z=2.001(5)z=2.001(5), which is consistent with the known value z=2z=2z=2, while for the site-diluted lattice we find z=3.90(1)z=3.90(1)z=3.90(1) or z=2.056(8)Dfz=2.056(8){D}_{f}z=2.056(8)Df​, where Df=91/48{D}_{f}=91/48Df​=91/48 is the fractal dimensionality of the percolating system. This is an improvement on previous estimates of z\ensuremath≈3.7z\ensuremath{\approx}3.7z\ensuremath≈3.7. The scaling results also show a fundamental difference between the two cases; for the 2D square lattice, the data can be collapsed onto a common scaling function even when \ensuremath⟨ms\ensuremath⟩\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}\ensuremath⟨ms​\ensuremath⟩ is relatively large, reflecting the Anderson tower of quantum rotor states with a common dynamic exponent z=2z=2z=2. For the diluted 2D square lattice, the scaling works well only for small \ensuremath⟨ms\ensuremath⟩\ensuremath{\langle}{m}_{s}\ensuremath{\rangle}\ensuremath⟨ms​\ensuremath⟩, indicating a mixture of different relaxation-time scalings between the low-energy states. Nevertheless, the low-energy dynamic here also corresponds to a tower of excitations.
We study the low-energy dynamics of S=1/2S=1/2S=1/2 antiferromagnetic Heisenberg clusters constructed by diluting a square lattice at vacancy concentration ppp 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 LLL 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)(S=0)(S=0) ground state. Here Df=91/48{D}_{f}=91/48Df​=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 zzz 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>0S>0S>0, scales with a smaller exponent than for the S=0S=0S=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>0S>0S>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=0S=0S=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.
We investigate the quantum dynamics of site diluted S=1/2 Heisenberg antiferromagnetic clusters at the 2D percolation threshold. We use Lanczos diagonalization to calculate the lowest excitation gap Delta and, to reach larger sizes, use quantum Monte Carlo simulations to study an upper bound for Delta obtained from sum rules involving the staggered structure factor and susceptibility. Scaling the gap distribution with the cluster length L, Delta approximately L(-), we obtain a dynamic exponent z approximately 2D(f), where D(f)=91/48 is the fractal dimensionality of the percolating cluster. This is in contrast with previous expectations of z=D(f). We argue that the low-energy excitations are due to weakly coupled effective moments formed due to local imbalance in sublattice occupation.
Quantum phase transition of site-diluted and bond-diluted Heisenberg antiferromagnets on square lattices is studied. By using the novel continuous-time loop algorithm, we perform quantum Monte Carlo simulations on quite larger lattices at extremely lower temperatures than the previous numerical studies. It is found that the antiferromagnetic long-range order at T = 0 persists so long as a cluster of magnetic sites percolates, that is, the critical concentration is equal to the classical percolation threshold, in both of the site-diluted and bond-diluted cases. Furthermore, we find that some critical exponents, such as the magnetization exponent β, are non-classical and strongly depend on the spin size S. On the other hand, we show that the correlation-length exponent ν is universal and is equal to the classical value (ν=4/3).
Ground-state phase transition of site-diluted Heisenberg antiferromagnets on a square lattice is studied. By using the continuous-time loop algorithm, we perform large-scale quantum Monte Carlo simulation on large systems at quite low temperatures. It is found that the critical concentration of magnetic sites is independent of the spin size S, and equal to the classical percolation threshold. However, the existence of quantum fluctuations makes the critical exponents deviate from those of the classical percolation transition. It is found that the transition is not universal, i.e., the critical exponents depend on the spin size S.
The ground-state parameters of the two-dimensional S=1/2S=1/2S=1/2 antiferromagnetic Heisenberg model are calculated using the stochastic series expansion quantum Monte Carlo method for $L\ifmmode\times\else\texttimes\fi{}L$ lattices with LLL up to 161616. The finite-size results for the energy EEE, the sublattice magnetization MMM, the long-wavelength susceptibility ${\ensuremath{\chi}}_{\ensuremath{\perp}}(q=2\ensuremath{\pi}/L)$, and the spin stiffness ${\ensuremath{\rho}}_{s},$ are extrapolated to the thermodynamic limit using fits to polynomials in 1/L1/L1/L, constrained by scaling forms previously obtained from renormalization-group calculations for the nonlinear $\ensuremath{\sigma}$ model and chiral perturbation theory. The results are fully consistent with the predicted leading finite-size corrections, and are of sufficient accuracy for extracting also subleading terms. The subleading energy correction $(\ensuremath{\sim}{1/L}^{4})$ agrees with chiral perturbation theory to within a statistical error of a few percent, thus providing numerical confirmation of the finite-size scaling forms to this order. The extrapolated ground- state energy per spin is $E=\ensuremath{-}0.669437(5)$. The result from previous Green's function Monte Carlo (GFMC) calculations is slightly higher than this value, most likely due to a small systematic error originating from ``population control'' bias in GFMC. The other extrapolated parameters are M=0.3070(3)M=0.3070(3)M=0.3070(3), ${\ensuremath{\rho}}_{s}=0.175(2)$, ${\ensuremath{\chi}}_{\ensuremath{\perp}}=0.0625(9)$, and the spin-wave velocity c=1.673(7)c=1.673(7)c=1.673(7). The statistical errors are comparable with those of previous estimates obtained by fitting loop algorithm quantum Monte Carlo data to finite-temperature scaling forms. Both MMM and ${\ensuremath{\rho}}_{s}$ obtained from the finite-TTT data are, however, a few error bars higher than the present estimates. It is argued that the T=0T=0T=0 extrapolations performed here are less sensitive to effects of neglected higher-order corrections, and therefore should be more reliable.
Ground-state magnetic properties of the diluted Heisenberg antiferromagnet on a square lattice are investigated by means of the quantum Monte Carlo method with the continuous-time loop algorithm. It is found that the critical concentration of magnetic sites is independent of the spin size S, and equal to the two-dimensional percolation threshold. However, the existence of quantum fluctuations makes the critical exponents deviate from those of the classical percolation transition. Furthermore, we found that the transition is not universal, i.e., the critical exponents significantly depend on S.