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International Journal of Modern Physics B

LINKED CLUSTER SERIES EXPANSIONS FOR TWO-PARTICLE STATES IN QUANTUM LATTICE MODELS

Weihong Zheng, Chris J. Hamer, Rajiv R. P. Singh, Simon Trebst, H. Monien

Published Nov 10, 2003• 0 citations
Publisher

Abstract

We have developed strong-coupling series expansion methods to study the two-particle spectra in quantum lattice models. The properties of bound states and multiparticle excitations can reveal important information about the dynamics of a given model. At the heart of this method lies the calculation of an effective Hamiltonian in the two-particle subspace. We use an orthogonal transformation to perform this block diagonalising, and find that maintaining orthogonality is crucial for cases where the ground state and the two-particle subspace have identical quantum numbers. The two-particle Schrödinger equation is solved by using a finite lattice approach in coordinate space or an integral equation in momentum space. These methods allow us to determine precisely the low-lying excitation spectra and dispersion relations for the two-particle bound states. The method has been tested for the (1+1) D transverse Ising model, and applied to the two-leg spin-1/2 Heisenberg ladder. We study the coherence lengths of the bound states, and how they merge with the two-particle continuum. Finally, these techniques are applied to the frustrated alternating Heisenberg chain, which has been of considerable recent interest due to its relevance to spin-Peierls systems such as CuGeO 3. Starting from a limit corresponding to weakly-coupled dimers, we develop high-order series expansions for the effective Hamiltonian in the two-particle subspace. In the regime of strong dimerisation, various properties of the singlet and triplet bound states, and the quintet antibound states, can be accurately calculated. We also study the behaviour as the external bond alternation vanishes, and the way in which the bound states of triplet dimer excitations make the transition to a soliton-antisoliton continuum.

DOI
10.1142/s0217979203020144

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We have developed strong-coupling series expansion methods to study the two-particle spectra in quantum lattice models. The properties of bound states and multiparticle excitations can reveal important information about the dynamics of a given model. At the heart of this method lies the calculation of an effective Hamiltonian in the two-particle subspace. We use an orthogonal transformation to perform this block diagonalising, and find that maintaining orthogonality is crucial for cases where the ground state and the two-particle subspace have identical quantum numbers. The two-particle Schrödinger equation is solved by using a finite lattice approach in coordinate space or an integral equation in momentum space. These methods allow us to determine precisely the low-lying excitation spectra and dispersion relations for the two-particle bound states. The method has been tested for the (1+1) D transverse Ising model, and applied to the two-leg spin-1/2 Heisenberg ladder. We study the coherence lengths of the bound states, and how they merge with the two-particle continuum. Finally, these techniques are applied to the frustrated alternating Heisenberg chain, which has been of considerable recent interest due to its relevance to spin-Peierls systems such as CuGeO 3. Starting from a limit corresponding to weakly-coupled dimers, we develop high-order series expansions for the effective Hamiltonian in the two-particle subspace. In the regime of strong dimerisation, various properties of the singlet and triplet bound states, and the quintet antibound states, can be accurately calculated. We also study the behaviour as the external bond alternation vanishes, and the way in which the bound states of triplet dimer excitations make the transition to a soliton-antisoliton continuum.
We develop strong-coupling series expansion methods to study two-particle spectra of quantum lattice models. At the heart of the method lies the calculation of an effective Hamiltonian in the two-particle subspace. We explicitly consider an orthogonality transformation to generate this block diagonalization, and find that maintaining orthogonality is crucial for systems where the ground state and the two-particle subspace are characterized by identical quantum numbers. We discuss the solution of the two-particle Schr\"odinger equation by using a finite lattice approach in coordinate space or by an integral equation in momentum space. These methods allow us to precisely determine the low-lying excitation spectra of the models at hand, including all two-particle bound/antibound states. Further, we discuss how to generate series expansions for the dispersions of the bound/antibound states. These allow us to employ series extrapolation techniques, whereby binding energies can be determined even when the expansion parameters are not small. We apply the method to the (1+1)-dimensional transverse Ising model and the two-leg $\mathrm{s}\mathrm{p}\mathrm{i}\mathrm{n}\ensuremath{-}\frac{1}{2}$ Heisenberg ladder. For the latter model, we also calculate the coherence lengths and determine the critical properties where bound states merge with the two-particle continuum.
We use recently developed strong-coupling expansion methods to study the two-particle spectra for the frustrated alternating Heisenberg model, consisting of an alternating nearest neighbor antiferromagnetic exchange and a uniform second neighbor antiferromagnetic exchange. Starting from the limit of weakly coupled dimers, we develop high order series expansions for the effective Hamiltonian in the two-particle subspace. In the limit of a strong applied dimerization, we calculate accurately various properties of singlet and triplet bound states and quintet antibound states. We also develop series expansions for bound state energies in various sectors, which can be extrapolated using standard methods to cases where the external bond alternation goes to zero. We study the properties of singlet and triplet bound states in the latter limit and suggest a crucial role for the bound states in the unbinding of triplets and deconfinement of spin-half excitations.
We present a new linked cluster expansion for calculating properties of multiparticle excitation spectra to high orders. We use it to obtain the two-particle spectra for systems of coupled spin-half dimers. We find that even for weakly coupled dimers the spectrum is very rich, consisting of many bound states. The number of bound states depends on both geometry of coupling and frustration. Many of the bound states can only be seen by going to sufficiently high orders in the perturbation theory, showing the extended character of the pair attraction.
We develop a linked cluster method to calculate the spectral weights of many-particle excitations at zero temperature. The dynamical structure factor is expressed as a sum of ``exclusive'' structure factors, each representing contributions from a given set of excited states. A linked cluster technique to obtain high-order series expansions for these quantities is discussed. We apply these methods to the alternating Heisenberg chain around the dimerized limit $(\ensuremath{\lambda}=0),$ where complete wave vector and frequency-dependent spectral weights for one- and two-particle excitations (continuum and bound states) are obtained. For small to moderate values of the interdimer coupling parameter $\ensuremath{\lambda},$ these lead to extremely accurate calculations of the dynamical structure factors. We also examine the variation of the relative spectral weights of one- and two-particle states with bond alternation all the way up to the limit of the uniform chain $(\ensuremath{\lambda}=1).$ In agreement with Schmidt and Uhrig, we find that the spectral weight is dominated by 2-triplet states even at $\ensuremath{\lambda}=1,$ which implies that a description in terms of triplet-pair excitations remains a good quantitative description of the system even for the uniform chain.
Cluster expansion methods are developed for calculating the spectral weight contributions of multiparticle excitations---continuum and bound states---to high orders. A complete 13th order calculation is carried out for the alternating Heisenberg chain. For $\ensuremath{\lambda}=0.27$, relevant to the material $\mathrm{C}\mathrm{u}({\mathrm{N}\mathrm{O}}_{3}{)}_{2}\ifmmode\cdot\else\textperiodcentered\fi{}2.5{\mathrm{D}}_{2}\mathrm{O}$, we present detailed spectral weights for the two-triplet continuum and all bound states. We also examine the variation of the relative weights of one- and two-particle states with bond alternation from the dimerized to the uniform chain limit.
In this thesis we describe a novel perturbative approach to low-dimensional quantum many-particle systems, which is based on continuous unitary transformations. We consider systems, which are defined on a lattice and allow a perturbative decomposition. The unperturbed part must have an equidistant spectrum -- the difference between two successive levels is called a quasi-particle. In this case the perturbative transformation leads to an effective Hamiltonian, which conserves the number of particles. The same transformation is used to also derive the effective counterparts of other, experimentally relevant observables. The effective operators are obtained as series expansions in the (small) perturbation parameter. In each order we find a set of products of ladder-operators, which act on states uniquely defined by the number of quasi-particles and their position in the lattice. Thus all calculations can be done in real space. The mathematical structure of the effective operators is extensively analysed. We additionally give all details necessary to implement the method on a computer, which allows the calculation of the effective quantities up to high orders. The method facilitates quantitative calculations of multi-particle excitations and spectral densities of experimentally relevant observables. We include a comprehensive application of the method to the two-dimensional Shastry-Sutherland model, a strongly frustrated quantum spin system. The model has experience an experimental realization by SrCu2(BO3)2. The limit of strong dimerization serves as starting point. Here the ground state is given by singlets on all dimers -- a single triplet constitutes an elementary excitation, i.e. quasi-particle. We quantitatively calculate the one- and two-triplet energies as well as the spectral densities of the Raman and neutron scattering operators. The findings for the spectral densities in particular represent new results. Comparing them to experimental data leads to interesting insights into the spectral properties of low-dimensional quantum spin systems.