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

Journal of Physics Condensed Matter

The resonating-valence-bond state; the singlet ground state

Igor V. Abarenkov

Published Sep 12, 1994• 1 citation
Publisher

Abstract

The resonating-valence-bond (RVB) State with one localized state per site is a state in which correlations are important and therefore for its determination it is necessary to go beyond the one-determinant approximation. Although the number of one-electron space orbitals is equal to the number of electrons, N, the number of necessary determinants increases factorially with N, thus making a rigorous treatment of the correlation effects impracticable even for systems containing relatively small number of electrons. On the other hand, by introducing a many-electron spin function a coupled system of equations for one-electron localized non-orthogonal space orbitals and N-electron spin function can be obtained which can be solved in practice. In this procedure the main difficulty resides in the equation for the N-electron spin function. In this paper it is shown that a perturbation theory based on the decomposition of the spin system into clusters, when taken beyond the first order can, in general, offer a suitable method of mapping the results of numerical calculations of spin clusters onto the total system.

DOI
10.1088/0953-8984/6/37/006

Related papers

TRANSFER-MATRIX METHOD FOR SOLVING THE SPIN 1/2 ANTIFERROMAGNETIC HEISENBERG CHAIN

M. A. García‐Bach, Daniel Klein, Roser Valentí

Following the discovery of high Tc superconductivity in the copper oxides, there has been a great deal of interest in the RVB wave function proposed by Anderson [1]. As a warm-up exercise we have considered a valence-bond wave function for the one dimensional spin-1/2 Heisenberg chain. The main virtue of our work is to propose a new variational singlet wavefunction which is almost analytically tractable by a transfer-matrix technique. We have obtained the ground state energy for finite as well as infinite chains, in good agreement with exact results. Correlation functions, excited states, and the effects of other interactions (e.g., spin-Peierls) are also accessible within this scheme [2]. Since the ground state of the chain is known to be a singlet (Lieb & Mattis [3]), we write the appropriate wave function as a superposition of valence-bond singlets, [Formula: see text], where | k > is a spin configuration obtained by pairing all spins into singlet pairs, in a way which is common in valence-bond calculations of large molecules. As in that case, each configuration, | k >, can be represented by a Rümer diagram, with directed bonds connecting each pair of spins on the chain. The c k 's are variational co-efficients, the form of which is determined as follows: Each singlet configuration (Rümer diagram) is divided into "zones", a "zone" corresponding to the region between two consecutive sites. Each zone is indexed by its distance from the end of the chain and by the number of bonds crossing it. Our procedure assigns a variational parameter, x ij , to the j th zone, when crossed by i bonds. The resulting wavefunction for an N-site chain is written as [Formula: see text] where m ij(k) equals 1 when zone j is crossed by i bonds and zero otherwise. To make the calculation tractable we reduce the number of variational parameters by disallowing configurations with bonds connecting any two sites separated by more than 2M lattice points. (For simplicity, we have limited ourselves to M=3, but the scheme can be used for any M). With the simple ansatz, matrix elements can be calculated by a transfer-matrix method. To understand the transfer-matrix method note that since only local zone parameters appear in the description of each state | k >, matrix elements and overlaps, [Formula: see text] and < k | k '>, are completely specified by a small number of "local states" associated with each zone. Within a given zone a local state is defined by (i) the number of bonds crossing the zone and (ii), by whether the bonds originate from the initial (| k >) or final (| k '>) state. It is then easy to see that "local states" of consecutive zones are connected by a 15 × 15 transfer matrix (for the case M=3). Furthermore, the overlap matrix element can be written as a product of transfer-matrices associated with each zone of the chain. When calculating matrix elements of the Hamiltonian, an additional matrix, U , must be defined, to represent the particular zone involving the two spins connected by the Heisenberg interaction. The relevant details as well as the comparison with exact results will be given elsewhere. We are planning to ultimately apply this method to the two dimensional case, and hope to include the effects of holes.

International Journal of Modern Physics B•Oct 1, 1988•2 citations

Theory of the Resonating Valence Bond in Quantum Spin System

Takehiko Oguchi, Hidetsugu Kitatani

The theory of the resonating valence bond (RVB) for the antiferromagnetic Heisenberg model of spin 1/2 proposed by Anderson is generalized by taking account of singlet bonds connecting distant spins, and is solved exactly for the finite lattice. It is shown that the RVB wave function is S tot (total spin quantum number)=0, and that replacing a part of singlet bonds by triplet bonds, eigenfunctions with S tot =1, 2, … can be constructed. These are the new representation of eigenfunctions of the Heisenberg Hamiltonian.

Journal of the Physical Society of Japan•Apr 1, 1989•25 citations

Resonating Valence Bond Theory of Coupled Heisenberg Chains

Steven R. White, R. M. Noack, Douglas J. Scalapino

Using numerical results from a density matrix renormalization group study as a guide, we develop a resonating valence bond (RVB) theory for coupled Heisenberg chains. We argue that simple topological effects mandate a short-range RVB description of systems with an even number of chains ${n}_{c}$, with a spin gap, short-range correlations, and confinement of topological spin defects. Odd-${n}_{c}$ systems have long-range RVB ground states, no gap, and power-law correlations.

arXiv:cond-mat/9403042•Physical Review Letters•Aug 8, 1994•405 citations

A renormalised hamiltonian approach for a resonant valence bond wavefunction

F. C. Zhang, Claudius Gros, Thomas Maurice Rice +1 more

The effective Hamiltonian of strongly correlated electrons on a square lattice is replaced by a renormalised Hamiltonian and the factors that renormalise the kinetic energy of holes and the Heisenberg spin-spin coupling are calculated using a Gutzwiller approximation scheme. The accuracy of this renormalisation procedure is tested numerically and found to be qualitatively excellent. Within the scheme a resonant valence bond (RVB) wavefunction is found at half-filling to be lower in energy than the antiferromagnetic state. If the wavefunction is expressed in fermion operators, local SU(2) and U(l) invariance leads to a redundancy in the representation. The introduction of holes removes these local invariances and we find that a d-wave RVB state is lowest in energy. This state has a superconducting order parameter whose amplitude is linear in the density of holes.

arXiv:cond-mat/0311604•Nov 26, 2003•1 citation

Properties of resonating-valence-bond spin liquids and critical dimer models

Ying Tang, Anders W. Sandvik, Christopher L. Henley

We use Monte Carlo simulations to study properties of Anderson's resonating-valence-bond (RVB) spin-liquid state on the square lattice (i.e., the equal superposition of all pairing of spins into nearest-neighbor singlet pairs) and compare with the classical dimer model (CDM). The latter system also corresponds to the ground state of the Rokhsar-Kivelson quantum dimer model at its critical point. We find that, although spin-spin correlations decay exponentially in the RVB, four-spin valence-bond-solid correlations are critical, qualitatively like the well-known dimer-dimer correlations of the CDM, but decaying more slowly (as $1/{r}^{\ensuremath{\alpha}}$ with $\ensuremath{\alpha}\ensuremath{\approx}1.20$, compared with $\ensuremath{\alpha}=2$ for the CDM). We also compute the distribution of monomer (defect) pair separations, which decay by a larger exponent in the RVB than in the CDM. We further study both models in their different winding-number sectors and evaluate the relative weights of different sectors. Like the CDM, all the observed RVB behaviors can be understood in the framework of a mapping to a ``height'' model characterized by a gradient-squared stiffness constant $K$. Four independent measurements consistently show a value ${K}_{\mathrm{RVB}}\ensuremath{\approx}1.6{K}_{\mathrm{CDM}}$, with the same kinds of numerical evaluations of ${K}_{\mathrm{CDM}}$ giving results in agreement with the rigorously known value ${K}_{\mathrm{CDM}}=\ensuremath{\pi}/16$. The background of a nonzero winding-number gradient $W/L$ introduces spatial anisotropies and an increase in the effective $K$, both of which can be understood as a consequence of anharmonic terms in the height-model free energy, which are of relevance to the recently proposed scenario of ``Cantor deconfinement'' in extended quantum dimer models. In addition to the standard case of short bonds only, we also studied ensembles in which fourth-neighbor (bipartite) bonds are allowed at a density controlled by a tunable fugacity, resulting (as expected) in a smooth reduction of $K$.

arXiv:1010.6146•Physical Review B•Nov 21, 2011•69 citations

A renormalised Hamiltonian approach to a resonant valence bond wavefunction

Fu‐Chun Zhang, Claudius Gros, Thomas Maurice Rice +1 more

The effective Hamiltonian of strongly correlated electrons on a square lattice is replaced by a renormalised Hamiltonian and the factors that renormalise the kinetic energy of holes and the Heisenberg spin-spin coupling are calculated using a Gutzwiller approximation scheme. The accuracy of this renormalisation procedure is tested numerically and found to be qualitatively excellent. Within the scheme a resonant valence bond (RVB) wavefunction is found at half-filling to be lower in energy than the antiferromagnetic state. If the wavefunction is expressed in fermion operators, local SU(2) and U(1) invariance leads to a redundancy in the representation. The introduction of holes removes these local invariances and the authors find that a d-wave RVB state is lowest in energy. This state has a superconducting order parameter whose amplitude is linear in the density of holes.

Superconductor Science and Technology•Jun 1, 1988•560 citations
The resonating-valence-bond (RVB) State with one localized state per site is a state in which correlations are important and therefore for its determination it is necessary to go beyond the one-determinant approximation. Although the number of one-electron space orbitals is equal to the number of electrons, N, the number of necessary determinants increases factorially with N, thus making a rigorous treatment of the correlation effects impracticable even for systems containing relatively small number of electrons. On the other hand, by introducing a many-electron spin function a coupled system of equations for one-electron localized non-orthogonal space orbitals and N-electron spin function can be obtained which can be solved in practice. In this procedure the main difficulty resides in the equation for the N-electron spin function. In this paper it is shown that a perturbation theory based on the decomposition of the spin system into clusters, when taken beyond the first order can, in general, offer a suitable method of mapping the results of numerical calculations of spin clusters onto the total system.
Following the discovery of high Tc superconductivity in the copper oxides, there has been a great deal of interest in the RVB wave function proposed by Anderson [1]. As a warm-up exercise we have considered a valence-bond wave function for the one dimensional spin-1/2 Heisenberg chain. The main virtue of our work is to propose a new variational singlet wavefunction which is almost analytically tractable by a transfer-matrix technique. We have obtained the ground state energy for finite as well as infinite chains, in good agreement with exact results. Correlation functions, excited states, and the effects of other interactions (e.g., spin-Peierls) are also accessible within this scheme [2]. Since the ground state of the chain is known to be a singlet (Lieb & Mattis [3]), we write the appropriate wave function as a superposition of valence-bond singlets, [Formula: see text], where | k > is a spin configuration obtained by pairing all spins into singlet pairs, in a way which is common in valence-bond calculations of large molecules. As in that case, each configuration, | k >, can be represented by a Rümer diagram, with directed bonds connecting each pair of spins on the chain. The c k 's are variational co-efficients, the form of which is determined as follows: Each singlet configuration (Rümer diagram) is divided into "zones", a "zone" corresponding to the region between two consecutive sites. Each zone is indexed by its distance from the end of the chain and by the number of bonds crossing it. Our procedure assigns a variational parameter, x ij , to the j th zone, when crossed by i bonds. The resulting wavefunction for an N-site chain is written as [Formula: see text] where m ij(k) equals 1 when zone j is crossed by i bonds and zero otherwise. To make the calculation tractable we reduce the number of variational parameters by disallowing configurations with bonds connecting any two sites separated by more than 2M lattice points. (For simplicity, we have limited ourselves to M=3, but the scheme can be used for any M). With the simple ansatz, matrix elements can be calculated by a transfer-matrix method. To understand the transfer-matrix method note that since only local zone parameters appear in the description of each state | k >, matrix elements and overlaps, [Formula: see text] and < k | k '>, are completely specified by a small number of "local states" associated with each zone. Within a given zone a local state is defined by (i) the number of bonds crossing the zone and (ii), by whether the bonds originate from the initial (| k >) or final (| k '>) state. It is then easy to see that "local states" of consecutive zones are connected by a 15 × 15 transfer matrix (for the case M=3). Furthermore, the overlap matrix element can be written as a product of transfer-matrices associated with each zone of the chain. When calculating matrix elements of the Hamiltonian, an additional matrix, U , must be defined, to represent the particular zone involving the two spins connected by the Heisenberg interaction. The relevant details as well as the comparison with exact results will be given elsewhere. We are planning to ultimately apply this method to the two dimensional case, and hope to include the effects of holes.
The theory of the resonating valence bond (RVB) for the antiferromagnetic Heisenberg model of spin 1/2 proposed by Anderson is generalized by taking account of singlet bonds connecting distant spins, and is solved exactly for the finite lattice. It is shown that the RVB wave function is S tot (total spin quantum number)=0, and that replacing a part of singlet bonds by triplet bonds, eigenfunctions with S tot =1, 2, … can be constructed. These are the new representation of eigenfunctions of the Heisenberg Hamiltonian.
Using numerical results from a density matrix renormalization group study as a guide, we develop a resonating valence bond (RVB) theory for coupled Heisenberg chains. We argue that simple topological effects mandate a short-range RVB description of systems with an even number of chains nc{n}_{c}nc​, with a spin gap, short-range correlations, and confinement of topological spin defects. Odd-nc{n}_{c}nc​ systems have long-range RVB ground states, no gap, and power-law correlations.
The effective Hamiltonian of strongly correlated electrons on a square lattice is replaced by a renormalised Hamiltonian and the factors that renormalise the kinetic energy of holes and the Heisenberg spin-spin coupling are calculated using a Gutzwiller approximation scheme. The accuracy of this renormalisation procedure is tested numerically and found to be qualitatively excellent. Within the scheme a resonant valence bond (RVB) wavefunction is found at half-filling to be lower in energy than the antiferromagnetic state. If the wavefunction is expressed in fermion operators, local SU(2) and U(l) invariance leads to a redundancy in the representation. The introduction of holes removes these local invariances and we find that a d-wave RVB state is lowest in energy. This state has a superconducting order parameter whose amplitude is linear in the density of holes.
We use Monte Carlo simulations to study properties of Anderson's resonating-valence-bond (RVB) spin-liquid state on the square lattice (i.e., the equal superposition of all pairing of spins into nearest-neighbor singlet pairs) and compare with the classical dimer model (CDM). The latter system also corresponds to the ground state of the Rokhsar-Kivelson quantum dimer model at its critical point. We find that, although spin-spin correlations decay exponentially in the RVB, four-spin valence-bond-solid correlations are critical, qualitatively like the well-known dimer-dimer correlations of the CDM, but decaying more slowly (as $1/{r}^{\ensuremath{\alpha}}$ with $\ensuremath{\alpha}\ensuremath{\approx}1.20$, compared with $\ensuremath{\alpha}=2$ for the CDM). We also compute the distribution of monomer (defect) pair separations, which decay by a larger exponent in the RVB than in the CDM. We further study both models in their different winding-number sectors and evaluate the relative weights of different sectors. Like the CDM, all the observed RVB behaviors can be understood in the framework of a mapping to a ``height'' model characterized by a gradient-squared stiffness constant KKK. Four independent measurements consistently show a value ${K}_{\mathrm{RVB}}\ensuremath{\approx}1.6{K}_{\mathrm{CDM}}$, with the same kinds of numerical evaluations of KCDM{K}_{\mathrm{CDM}}KCDM​ giving results in agreement with the rigorously known value ${K}_{\mathrm{CDM}}=\ensuremath{\pi}/16$. The background of a nonzero winding-number gradient W/LW/LW/L introduces spatial anisotropies and an increase in the effective KKK, both of which can be understood as a consequence of anharmonic terms in the height-model free energy, which are of relevance to the recently proposed scenario of ``Cantor deconfinement'' in extended quantum dimer models. In addition to the standard case of short bonds only, we also studied ensembles in which fourth-neighbor (bipartite) bonds are allowed at a density controlled by a tunable fugacity, resulting (as expected) in a smooth reduction of KKK.
The effective Hamiltonian of strongly correlated electrons on a square lattice is replaced by a renormalised Hamiltonian and the factors that renormalise the kinetic energy of holes and the Heisenberg spin-spin coupling are calculated using a Gutzwiller approximation scheme. The accuracy of this renormalisation procedure is tested numerically and found to be qualitatively excellent. Within the scheme a resonant valence bond (RVB) wavefunction is found at half-filling to be lower in energy than the antiferromagnetic state. If the wavefunction is expressed in fermion operators, local SU(2) and U(1) invariance leads to a redundancy in the representation. The introduction of holes removes these local invariances and the authors find that a d-wave RVB state is lowest in energy. This state has a superconducting order parameter whose amplitude is linear in the density of holes.