Spin Dynamics in the One-Dimensional Antiferromagnet (CD3)4 NMnCl3

Abstract
Recent studies of the instantaneous magnetic correlations in (CD3)4NMnCl3 using quasielastic-neutron-scattering techniques have shown that the MnCl3 chains in this compound exhibit purely one-dimensional paramagnetic behavior down to 1.1 °K. The interactions between Mn2+ ions along the chain are such that a molecular field theory would predict an ordering at ∼ 76 °K. It was found that both the spatial and thermal variation of the instantaneous correlations could be quantitatively accounted for using Fisher's theory for the classical Heisenberg linear chain. In this paper we report a detailed study of the time-dependent magnetic correlations in (CD3)4 NMnCl3 using inelastic—neutron-scattering techniques. It is bound that at low temperatures, for qκ and ω0, the Van Hove scattering function S(Q, ω) may be accurately described by spin-wave theory with a dispersion relation ω=6.1sinπqc*z meV over the entire one-dimensional Brillouin zone, even though there is no long-range order. As the temperature is increased from 1.9 to 40 °K these "spin waves" typically weaken in intensity and broaden asymmetrically, with the scattering increasing on the low-energy side. In no case were both well-defined spin waves and a central diffusive component observed simultaneously, although the latter, if weak, could have been masked by the large incoherent scattering.