Huge Transverse Magnetization in the Field-Induced Phase of the Antiferromagnetic Molecular Wheel CsFe8

The 1H-NMR spectrum and nuclear relaxation rate 1/T_1 in the antiferromagnetic wheel CsFe8 were measured to characterize the previously observed magnetic field-induced low-temperature phase around the level crossing at 8 T. The data show that the phase is characterized by a huge staggered transverse polarization of the electronic Fe spins, and the opening of a gap, providing microscopic evidence for the interpretation of the phase as a field-induced magneto-elastic instability.Comment: 5 pages, 4 figures, REVTEX4, to appear in PR

Heisenberg exchange parameters of molecular magnets from the high-temperature susceptibility expansion

We provide exact analytical expressions for the magnetic susceptibility function in the high temperature expansion for finite Heisenberg spin systems with an arbitrary coupling matrix, arbitrary single-spin quantum number, and arbitrary number of spins. The results can be used to determine unknown exchange parameters from zero-field magnetic susceptibility measurements without diagonalizing the system Hamiltonian. We demonstrate the possibility of reconstructing the exchange parameters from simulated data for two specific model systems. We examine the accuracy and stability of the proposed method.Comment: 13 pages, 7 figures, submitted to Phys. Rev.

Triplet Dispersion in CuGeO_3: Perturbative Analysis

We reconsider the 2d model for CuGeO_3 introduced previously (Phys. Rev. Lett. 79, 163 (1997)). Using a computer aided perturbation method based on flow equations we expand the 1-triplet dispersion up to 10th order. The expansion is provided as a polynom in the model parameters. The latter are fixed by fitting the theoretical result to experimental data obtained by INS. For a dimerization delta = 0.08(1) we find an excellent agreement with experiment. This value is at least 2 to 3 times higher than values deduced previously from 1d chain approaches. For the intrachain frustration alpha_0 we find a smaller value of 0.25(3). The existence of interchain frustration conjectured previously is confirmed by the analysis of temperature dependent susceptibility.Comment: 8 pages, 10 figures, submitted to Phys. Rev.

Spin dynamics in molecular ring nanomagnets: Significant effect of acoustic phonons and magnetic anisotropies

The nuclear spin-lattice relaxation rate 1/T_1_ is calculated for magnetic ring clusters by fully diagonalizing their microscopic spin Hamiltonians. Whether the nearest-neighbor exchange interaction J is ferromagnetic or antiferromagnetic, 1/T_1_ versus temperature T in ring nanomagnets may be peaked at around k_B_T=|J| provided the lifetime broadening of discrete energy levels is in proportion to T^3^. Experimental findings for ferromagnetic and antiferromagnetic Cu^II^ rings are reproduced with crucial contributions of magnetic anisotropies as well as acoustic phonons.Comment: 5 pages with 5 figures embedded, to be published in J. Phys. Soc. Jpn. 75, No. 10 (2006

Neutron scattering study of the field-induced soliton lattice in CuGeO3_3

CuGeO$_3$ undergoes a transition from a spin-Peierls phase to an incommensurate phase at a critical field of $H_c\approx 12.5$ T. In the high-field phase a lattice of solitons forms, with both structural and magnetic components, and these have been studied using neutron scattering techniques. Our results provide direct evidence for a long-ranged magnetic soliton structure which has both staggered and uniform magnetizations, and with amplitudes that are broadly in accord with theoretical estimates. The magnetic soliton width, $\Gamma$, and the field dependence of the incommensurability, $\delta k_{sp}$, are found to agree well with theoretical predictions.Comment: 5 pages, 3 figure

Q-dependence of the inelastic neutron scattering cross section for molecular spin clusters with high molecular symmetry

For powder samples of polynuclear metal complexes the dependence of the inelastic neutron scattering intensity on the momentum transfer Q is known to be described by a combination of so called interference terms. They reflect the interplay between the geometrical structure of the compound and the spatial properties of the wave functions involved in the transition. In this work, it is shown that the Q-dependence is strongly interrelated with the molecular symmetry of molecular nanomagnets, and, if the molecular symmetry is high enough, is actually completely determined by it. A general formalism connecting spatial symmetry and interference terms is developed. The arguments are detailed for cyclic spin clusters, as experimentally realized by e.g. the octanuclear molecular wheel Cr8, and the star like tetranuclear cluster Fe4.Comment: 8 pages, 1 figures, REVTEX