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arXiv:1206.6803 · Physical Review B

Correlated valence-bond states

Yu‐Cheng Lin, Ying Tang, Jie Lou, Anders W. Sandvik

Published Oct 10, 2012• 13 citations
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Abstract

We study generalizations of the singlet-sector amplitude-product (AP) states in the valence-bond basis of $S=1/2$ quantum spin systems. In the standard AP states, the weight of a tiling of the system into valence bonds (singlets of two spins) is a product of amplitudes depending on the length of the bonds. We here introduce correlated AP (CAP) states, in which the AP is further multiplied by factors depending on two bonds connected to a pair of sites (here nearest neighbors). While the standard AP states can describe a phase transition between an antiferromagnetic (N\'eel) state and a valence-bond solid (VBS) in one dimension (which we also study here), in two dimensions it cannot describe VBS order. With the CAP states, N\'eel-VBS transitions are realized as a function of some parameter describing the bond correlations. We here study such phase transitions of CAP wave functions on the square lattice. We find examples of direct first-order N\'eel-VBS transitions, as well as cases where there is an extended U(1) spin liquid phase intervening between the N\'eel and VBS states. In the latter case the transitions are continuous and we extract critical exponents and address the issue of a possible emergent U(1) symmetry in the near-critical VBS. We also consider variationally optimized CAP states for the standard Heisenberg model in one and two dimensions and the $J$-$Q$ model in two dimensions, with the latter including four-spin interactions ($Q$) in addition to the Heisenberg exchange ($J$) and harboring VBS order for large $Q/J$. The optimized CAP states lead to significantly lower variational energies than the simple AP states for these models.

DOI
10.1103/physrevb.86.144405

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We study generalizations of the singlet-sector amplitude-product (AP) states in the valence-bond basis of S=1/2S=1/2S=1/2 quantum spin systems. In the standard AP states, the weight of a tiling of the system into valence bonds (singlets of two spins) is a product of amplitudes depending on the length of the bonds. We here introduce correlated AP (CAP) states, in which the AP is further multiplied by factors depending on two bonds connected to a pair of sites (here nearest neighbors). While the standard AP states can describe a phase transition between an antiferromagnetic (N'eel) state and a valence-bond solid (VBS) in one dimension (which we also study here), in two dimensions it cannot describe VBS order. With the CAP states, N'eel-VBS transitions are realized as a function of some parameter describing the bond correlations. We here study such phase transitions of CAP wave functions on the square lattice. We find examples of direct first-order N'eel-VBS transitions, as well as cases where there is an extended U(1) spin liquid phase intervening between the N'eel and VBS states. In the latter case the transitions are continuous and we extract critical exponents and address the issue of a possible emergent U(1) symmetry in the near-critical VBS. We also consider variationally optimized CAP states for the standard Heisenberg model in one and two dimensions and the JJJ-QQQ model in two dimensions, with the latter including four-spin interactions (QQQ) in addition to the Heisenberg exchange (JJJ) and harboring VBS order for large Q/JQ/JQ/J. The optimized CAP states lead to significantly lower variational energies than the simple AP states for these models.
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We study the S=1/2S=1/2S=1/2 Heisenberg (JJJ) model on the two-dimensional (2D) square lattice in the presence of additional higher-order spin interactions (QQQ) which lead to a valence-bond-solid (VBS) ground state. Using quantum Monte Carlo simulations, we analyze the thermal VBS transition. We find continuously varying exponents, with the correlation-length exponent $\ensuremath{\nu}$ close to the Ising value for large Q/JQ/JQ/J and diverging when Q/JQ/JQ/J approaches the quantum-critical point (the critical temperature ${T}_{c}\ensuremath{\rightarrow}0$). We identify the transition with a class of conformal field theories with charge c=1c=1c=1 and critical exponents varying between those of the 2D Ising model and the Kosterlitz-Thouless (KT) fixed point. We find explicit evidence for KT physics by studying the emergence of U(1)U(1)U(1) symmetry of the order parameter at T=TcT={T}_{c}T=Tc​ when ${T}_{c}\ensuremath{\rightarrow}0$.
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We calculate the bipartite von Neumann and second R\'enyi entanglement entropies of the ground states of spin-1/2 dimerized Heisenberg antiferromagnets on a square lattice. Two distinct dimerization patterns are considered: columnar and staggered. In both cases, we concentrate on the valence bond solid (VBS) phase and describe such a phase with the bond-operator representation. Within this formalism, the original spin Hamiltonian is mapped into an effective interacting boson model for the triplet excitations. We study the effective Hamiltonian at the harmonic approximation and determine the spectrum of the elementary triplet excitations. We then follow an analytical procedure, which is based on a modified spin-wave theory for finite systems and was originally employed to calculate the entanglement entropies of magnetic ordered phases, and calculate the entanglement entropies of the VBS ground states. In particular, we consider one-dimensional (line) subsystems within the square lattice, a choice that allows us to consider line subsystems with sizes up to ${L}^{\ensuremath{'}}\phantom{\rule{0.16em}{0ex}}=\phantom{\rule{0.16em}{0ex}}1000$. We combine such a procedure with the results of the bond-operator formalism at the harmonic level and show that, for both dimerized Heisenberg models, the entanglement entropies of the corresponding VBS ground states obey an area law as expected for gapped phases. For both columnar-dimer and staggered-dimer models, we also show that the entanglement entropies increase but they seem to not diverge as the dimerization decreases and the system approaches the N\'eel-VBS quantum phase transition. Finally, the entanglement spectra associated with the VBS ground states are presented.