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.
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.
We describe a Peierls dimerization which occurs in ferromagnetic spin chains at finite temperature, within the modified spin-wave theory. Usual spin-wave theory is modified by introducing a Lagrange multiplier which enforces a nonmagnetic state at finite temperature. It is shown that this method gives results in excellent agreement with the density–matrix renormalization group applied to transfer matrices for dimerized ferromagnetic chains. We study bond correlation functions ( S i · S i+1 ) and explore the characteristic features of dimerization in the specific heat.
Thermodynamic properties of the quantum Heisenberg spin chains with S=1/2, 1, and 3/2 are investigated using the transfer-matrix renormalization-group method. The temperature dependence of the magnetization, susceptibility, specific heat, spin-spin correlation length, and several other physical quantities in a zero or finite applied field are calculated and compared. Our data agree well with the Bethe ansatz, exact diagonalization, and quantum Monte Carlo results and provide further insight into the quantum effects in the antiferromagnetic Heisenberg spin chains.
The effect of dimerization on the random antiferomagnetic Heisenberg chain with spin 1/2 is studied by the density matrix renormalization group method. The ground state energy, the energy gap distribution and the string order parameter are calculated. Using the finite size scaling analysis, the dimerization dependence of the these quantities are obtained. The ground state energy gain due to dimerization behaves as u a with a > 2 where u denotes the degree of dimerization, suggesting the absence of spin-Peierls instability. It is explicitly shown that the string long range order survives even in the presence of randomness. The string order behaves as u 2β with β∼0.37 in agreement with the recent prediction of real space renormalization group theory (β=(3−5)/2≃0.382). The physical picture of this behavior in this model is also discussed.
The magnetization process, the susceptibility, and the specific heat of the spin-1∕2 antiferromagnet (AF)-AF-ferromagnet (F) and F-F-AF trimerized quantum Heisenberg chains have been investigated by means of the transfer matrix renormalization group (TMRG) technique as well as the modified spin-wave (MSW) theory. A magnetization plateau at m=1∕6 for both trimerized chains is observed at low temperature. The susceptibility and the specific heat show various behaviors for different ferromagnetic and antiferromagnetic interactions and in different magnetic fields. The TMRG results of susceptibility and the specific heat can be nicely fitted by a linear superposition of double two-level systems, where two fitting equations are proposed. Three branch excitations, one gapless excitation and two gapful excitations, for both systems are found within the MSW theory. It is observed that the MSW theory captures the main characteristics of the thermodynamic behaviors at low temperatures. The TMRG results are also compared with the possible experimental data.
Abstract In this work, we present a comparative study of thermodynamic quantum equilibrium observables of spin-1 Heisenberg chain. As a theoretical approach, the modified spin-wave theory is chosen. From the numerical side, we consider finite-temperature Lanczos, kernel polynomial, and density matrix renormalization techniques. The results show general consistency of thermodynamic quantities, such as heat capacity and magnetic susceptibility, calculated within the approaches. For the modified spin-wave, the results show some inaccuracy especially at low temperature, failure in capturing the gapped features of spin-1 Heisenberg chain, while the numerical approaches illustrate a good achievement at T→0 T → 0 within the proper parameters chosen.
The magnetic and thermodynamic properties of spin-1∕2 Heisenberg diamond chains are investigated in three different cases: (a) J1, J2, J3>0 (frustrated), (b) J1, J3<0, J2>0 (frustrated), and (c) J1, J2>0, J3<0 (nonfrustrated), where the bond coupling Ji(i=1,2,3)>0 stands for an antiferromagnetic (AF) interaction, and <0 for a ferromagnetic (F) interaction. The density-matrix renormalization-group (DMRG) technique is invoked to study the properties of the system in the ground state, while the transfer-matrix renormalization-group (TMRG) technique is applied to explore the thermodynamic properties. The local magnetic moments, spin-correlation functions, and static structure factors are discussed in the ground state for the three cases. It is shown that the static structure factor S(q) shows peaks at wave vectors $q=a\ensuremath{\pi}∕3$ (a=0,1,2,3,4,5) for different couplings in a zero magnetic field, which, however, in the magnetic fields where the magnetization plateau with m=1∕6 pertains, exhibits the peaks only at q=0, $2\ensuremath{\pi}∕3$, and $4\ensuremath{\pi}∕3$, which are found to be couplings independent. The DMRG results of the zero-field static structure factor can be nicely fitted by a linear superposition of six modes, where two fitting equations are proposed. It is observed that the six modes are closely related to the low-lying excitations of the system. At finite temperatures, the magnetization, susceptibility, and specific heat show various behaviors for different couplings. The double-peak structures of the susceptibility, and specific heat against temperature are obtained, where the peak positions and heights are found to depend on the competition of the couplings. It is also uncovered that the XXZ anisotropy of F and AF couplings leads the system of case (c) to display quite different behaviors. In addition, the experimental data of the susceptibility, specific heat, and magnetization for the compound Cu3(CO3)2(OH)2 are fairly compared with our TMRG results.