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Abstract:

The molecular magnet Hpyr [Fe17 O16 (OH) 12 (py) 12 Br4] Br4 (" Fe17 ") has a well-defined cluster spin ground state of S=35/2 at low temperatures and an axial molecular anisotropy of only D-0.02K. Dipolar interactions between the molecular spins induce long-range magnetic order below 1.1 K. We report here the magnetic structure of Fe17, as determined by unpolarized neutron diffraction experiments performed on a polycrystalline sample of deuterated Fe17 in zero applied magnetic field. In addition, we report bulk susceptibility, magnetization, and specific heat data. The temperature dependence of the long-range magnetic order has been tracked and is well accounted for within mean-field theory. Ferromagnetic order along the crystallographic c axis of the molecular spins, as determined by the neutron diffraction experiments, is in agreement with ground-state dipolar energy calculations. © 2008 The American Physical Society.

Abstract:

The commensurate phase of multiferroic HoMn2O5 was studied by X-ray magnetic scattering, both off resonance and in resonant conditions at the Ho-L3 edge. Below 40 K, magnetic ordering at the Ho sites is induced by the main Mn magnetic order parameter, and its temperature dependence is well accounted for by a simple Curie-Weiss susceptibility model. A lattice distortion of periodicity twice that of the magnetic order is also evidenced. Azimuthal scans confirm the model of the magnetic structure recently refined from neutron diffraction data for both Mn and Ho sites, indicating that the two sublattices interact via magnetic superexchange.