Modeling the spin-Peierls transition of spin-1/2 chains with correlated states: J1-J2 model, CuGeO3 and TTF-CuS4C4(CF3)4
Abstract
The spin-Peierls transition at TSP of spin-1/2 chains with isotropic exchange interactions has previously been modeled as correlated for T > TSP and mean field for T < TSP. We use correlated states throughout in the J1-J2 model with antiferromagnetic exchange J1 and J2 = α J1 between first and second neighbors, respectively, and variable frustration 0 ≤ α ≤ 0.50. The thermodynamic limit is reached at high T by exact diagonalization of short chains and at low T by density matrix renormalization group calculations of progressively longer chains. In contrast to mean field results, correlated states of 1D models with linear spin-phonon coupling and a harmonic adiabatic lattice provide an internally consistent description in which the parameter TSP yields both the stiffness and the lattice dimerization δ(T). The relation between TSP and (δ,α), the T = 0 gap induced by dimerization, depends strongly on α and deviates from the BCS gap relation that holds in uncorrelated spin chains. Correlated states account quantitatively for the magnetic susceptibility of TTF-CuS4C4(CF3)4 crystals (J1 = 79 K, α = 0, TSP = 12 K) and CuGeO3 crystals (J1 = 160 K, α = 0.35, TSP = 14 K). The same parameters describe the specific heat anomaly of CuGeO3 and inelastic neutron scattering. Modeling the spin-Peierls transition with correlated states exploits the fact that δ(0) limits the range of spin correlations at T = 0 while T > 0 limits the range at δ= 0.