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Journal of Physics Condensed Matter

Static and dynamic properties of a dimerized quantum-spin chain

Oliver Fritz, Stephen William Lovesey, Greg I Watson

Published Jul 20, 1998• 1 citation
Publisher

Abstract

Various static spin-correlation functions and the weights of the spin excitations, or collective normal modes, in the van Hove response function, observed in neutron scattering experiments, are calculated as a function of temperature for a model quantum-spin chain. The spins interact through an isotropic Heisenberg exchange that extends to nearest-neighbour spins. In our model, spins of magnitude 1/2 form a dimerized chain with alternating exchange interactions. We explore the static and dynamic properties for ferromagnetic and antiferromagnetic exchange interactions. Results for the various properties are shown to be exact in the limit of a high temperature, and we argue that the results are very good at low temperatures. Unlike the case for linear spin-wave theory, the results are also exact in the limit of strong dimerization, i.e. non-interacting coupled pairs of spins.

DOI
10.1088/0953-8984/10/28/013

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Various static spin-correlation functions and the weights of the spin excitations, or collective normal modes, in the van Hove response function, observed in neutron scattering experiments, are calculated as a function of temperature for a model quantum-spin chain. The spins interact through an isotropic Heisenberg exchange that extends to nearest-neighbour spins. In our model, spins of magnitude 1/2 form a dimerized chain with alternating exchange interactions. We explore the static and dynamic properties for ferromagnetic and antiferromagnetic exchange interactions. Results for the various properties are shown to be exact in the limit of a high temperature, and we argue that the results are very good at low temperatures. Unlike the case for linear spin-wave theory, the results are also exact in the limit of strong dimerization, i.e. non-interacting coupled pairs of spins.
We present low-temperature static and dynamic properties of the quantum one-dimensional isotropic integer spin Heisenberg magnet with antiferromagnetic nearest-neighbour (nn) and next-nearest-neighbour (nnn) interactions. The modified spin-wave theory is used to provide quantities such as the spin-wave dispersion relation, the ground-state energy, the gap and its dependence with temperature, and the asymptotic behaviour of the spin–spin correlation function. The ground state energy and the singlet–triplet energy gap are obtained for several values of j, defined as the ratio of the nnn interaction constant to the nn one. Our results show that the ground-state and the gap energies increase with j, in accordance with numerical results available in the literature. The calculation of the dynamic correlation function is performed using the projection operator formalism: the procedure includes up to two-magnon processes. We show that, depending on the values of the frustration parameter j, the wavevector and the temperature, a double-peak structure for the dynamical correlation function can develop.
Low-temperature magnetic properties of both classical and quantum dimerized ferromagnetic spin chains are studied. It is shown that at low temperatures the classical dimerized model reduces to the classical uniform model with the effective exchange integral ${J}_{0}=J(1\ensuremath{-}{\ensuremath{\delta}}^{2})$, where $\ensuremath{\delta}$ is the dimerization parameter. The partition function and spin correlation function are calculated by means of mapping to the continuum limit, which is justified at low temperatures. The quantum model is studied using the Dyson-Maleev representation of the spin operators. It is shown that in the long-wavelength limit the Hamiltonian of the quantum dimerized chain reduces to that of the uniform ferromagnetic chain with the effective exchange integral ${J}_{0}=J(1\ensuremath{-}{\ensuremath{\delta}}^{2})$. This fact implies that the known equivalence of the low-temperature magnetic properties of classical and quantum ferromagnetic chains remains for the dimerized chains. The considered model is generalized to include the next-neighbor antiferromagnetic interaction.
The research presented here focuses on the theoretical investigation of spinons in quasi one-dimensional quantum spin chains from the perspective of neutron scattering, with emphasis placed on the calculation of dynamic spin structure factors for both unpolarised and polarised incident neutrons. Two anisotropic versions of the Heisenberg spin chain are considered for such an examination: the spin-1/21/21/2 antiferromagnetic XXZXXZXXZ model and the spin-1/21/21/2 ferromagnetic XYZXYZXYZ model.The XYZXYZXYZ model supports spinon scattering (modelled at finite temperature) and is related to the so-called Villain mode. The introduction of a perturbation in the form of an external transverse magnetic field or Dzyaloshinskii-Moriya interaction (DMI) leads to the emergence of incommensurability in the system; such a result is a signature of fractional excitations. The presence of these interactions also give rise to a chiral response associated with the spinons in the polarised term of the scattering cross section. The inelastic scattering cross section is computed for both unpolarised and polarised neutrons.In relation to the antiferromagnetic XXZXXZXXZ model, emphasis is on spinon pair creation (modelled at T=0rmKT = 0 {rm K}T=0rmK). Motivated by the presence of a chiral response in the case of the XYZXYZXYZ model mentioned above, a new technique is developed in order to incorporate DMI and the transverse magnetic field so that one can determine if there is a chiral property associated with the two-spinon system. This technique is numerical in nature and is based on Green function methods. Using the results produced by the Green function approach, the inelastic cross section in the presence of an external transverse magnetic field is computed for the first time. The result is compared with experimental neutron scattering data; good agreement is demonstrated between theory and experiments on rmCsCoBr3{rm CsCoBr}_3rmCsCoBr3​.Finally, the Green function approach is generalised to account for the interactions between spin chains in magnetic compounds described by a staggered field. Various dynamic structure factors are computed for this scenario with results compared to experiment; good agreement between the theory and experiments on rmRbCoCl3{rm RbCoCl}_3rmRbCoCl3​ is shown.
Various forms of antiferromagnetic exchange interaction among quantized spins in one-dimensional and quasi-one-dimensional lattices are examined. Primary results are reported in two real compounds, the sodium vanadate NaV2O5 and the copper germanate CuGeO3, and in a class of compounds of real materials modeled as dimerized antiferromagnetically coupled spin-1/2 chains susceptible to spin-1 impurity doping and that include such examples as the strontium cuprate Sr14Cu24O41 and vanadium pyrophosphate (VO)2P2O7. Sodium vanadate, NaV2O5, a quarter-filled two-leg ladder compound that was originally thought to be composed of magnetic legs and nonmagnetic legs was subsequently shown to be a charge ordered system below room temperature. Initial models of the material as isolated antiferromagnetically coupled spin-1/2 chains can be mapped to the subsequently resolved magnetic system of the charge ordered state with the spins on molecular orbitals of V-O-V rungs antiferromagentically coupled between neighboring rungs either on the same ladder or on neighboring ladders. Comparing the model's dynamic structure factor to inelastic neutron scattering data could distinguish between the proposed spin coupling schemes and consequently reveal the details of the interaction between the lattice and the "zig-zag" charge density as well as the magnetic stabilization of the low temperature phase. Copper germanate, the first and only known inorganic spin-Peierls compound, exhibits a strong temperature dependent exchange coupling pattern among the spin-1/2 Cu2+ chains. Above the spin-Peierls transition temperature an unmodulated antiferromagnetic nearest neighbor exchange interaction J1 competes with an antiferromagnetic next nearest neighbor interaction J2. The next nearest neighbor exchange represents an effective coupling equivalent to the net effect of all longer range exchange interactions. This frustration to the nearest neighbor spin exchange produces a distinctive magnetic susceptibility χ (T) much different from the Bonner-Fisher susceptibility of the spin-1/2 Heisenberg chain with nearest neighbor antiferromagnetic exchange only. The ratio of the second to first nearest neighbor couplings α = J2/J1 ≈ 0.36 is sufficient to open a spontaneous gap in the spin-wave excitation spectrum at low temperatures. Below TSP = 14K, the dynamical structure factor is used to fit the dimerization δ and the exchange interactions J1 and J2 to the inelastic neutron scattering data of CuGeO3 at T = 10K. It is found that both δ and α increase significantly at lower temperatures, relative to the values obtained in the high temperature phase and at the onset of dimeration at 14 K. Static structure factor calculations how Scattering inconsistent with the δ−J1−J2 model and can be attributed primarily to the phonon degrees of freedom but possibly also to the couplings between chains in the b and a directions of the crystal lattice. Structurally dimerized compounds of antiferromagnetic spin-1/2 chains possess dynamic structure factor and magnetic susceptibility features that are very sensitive to doping with magnetic and nonmagnetic impurities. It is shown that the effects of spin-1 impurities are very similar to those of nonmagnetic (S = 0) impurities if the coupling between impurity and native spin is about the same magnitude as or larger than between native S = 1/2 spins. The microscopic origins of the similarity can be appreciated with the consideration that neighboring spins to the impurity find it more energetically favorable to couple to the impurity than the other spins of the lattice. Thus the spin-1 impurity and its neighboring S = 1/2 spins decouple from the lattice, creating a nonmagnetic break in the chain. The spins that now observe a nonmagnetic cluster on one side can couple to the S = 1/2 spins on the other side with a higher AF correlation than in the pure compound since they do not have to have a fluctuating dimer resonating between two neighbors. Such enhancements to the local correlations can stabilize the global AF order in one dimensional compounds as shown in theoretical and experimental studies of CuGeO3. ED calculations of the dynamic structure factor show that S(q, ω) developes states with ω = 0 in the gap at q = π. Magnetic susceptibilites in the presense of spin-1 impurities were obtained for 80 site chains by QMC simulations and for 16 site chains by ED calculations. An impurity concentration-dependent second peak in the low temperature region reveals an increasing second maximum with T as observed in doped copper germanates and suggests that the results of the study are applicable even to phonon mediated dimerization. This is not immediately apparent because spin-phonon coupling could distort the dimerization patterns. However, experimental and theoretical results show that elastic coupling between chains can stabilize the dimerization pattern due to the impurities and the results will still apply.
We present a study of the spin-1/2 Heisenberg chain with alternating ferro- and antiferromagnetic exchange, focusing on the role of the exchange couplings to cover both, dimer and Haldane limit. Employing a complementary combination of perturbation theory and quantum Monte Carlo simulation, we report results for the magnetic susceptibility as well as the dynamic structure factor over a wide range of coupling constants and for different temperatures to extract the spin gap. For a small ferromagnetic coupling, we find good agreement between perturbation theory and quantum Monte Carlo. For arbitrary exchange couplings we show that the dynamic structure factor, obtained from quantum Monte Carlo, scales between triplons and a Haldane chain spectrum. Finally, we contrast our findings for the spin gap versus the exchange couplings against existing literature.
Ferromagnetic, in contrast to antiferromagnetic, Heisenberg chains can undergo a spin-Peierls dimerization only at finite temperatures. They show reentrant behavior as a function of temperature, which might play a role for systems with small effective elastic constants as, for example, monatomic chains on surfaces. We investigate the physical properties of the dimerized ferromagnetic Heisenberg chain using a modified spin-wave theory. We calculate the exponentially decaying spin- and dimer-correlation functions, analyze the temperature dependence of the corresponding coherence lengths, the susceptibility, as well as the static and dynamic spin-structure factors. By comparing with numerical data obtained by the density-matrix renormalization group applied to transfer matrices, we find that the modified spin-wave theory yields excellent results for all these quantities for a wide range of dimerizations and temperatures.