X-ray and neutron scattering

Abstract:

We report neutron inelastic scattering measurements on polycrystalline LaFePO and Sr2ScO3FeP, two members of the iron phosphide families of superconductors. No evidence is found for any magnetic fluctuations in the spectrum of either material in the energy and wavevector ranges probed. Special attention is paid to the wavevector at which spin-density-wave-like fluctuations are seen in other iron-based superconductors. We estimate that the magnetic signal, if present, is at least a factor of four (Sr2ScO3FeP) or seven (LaFePO) smaller than in the related iron arsenide and chalcogenide superconductors. These results suggest that magnetic fluctuations are not as influential on the electronic properties of the iron phosphide systems as they are in other iron-based superconductors.

Abstract:

We report inelastic neutron scattering results that reveal an hour-glass magnetic excitation spectrum in La1.75Sr0.25CoO 4. The magnetic spectrum is similar to that observed previously in La1.67Sr0.33CoO4, but the spectral features are broader. We show that the spectrum of La1.75Sr 0.25CoO4 can be modelled by the spin dynamics of a system with a disordered cluster spin glass ground state. Bulk magnetization measurements are presented that support the proposed glassy ground state. The observations reiterate the importance of quasi-one-dimensional magnetic correlations and disorder for the hour-glass spectrum, and suggest that disordered spin and charge stripes exist at lower doping in La 2-xSrxCoO4 than previously thought. © 2013 American Physical Society.

Abstract:

The zeolitic imidazolate framework ZIF-4 undergoes an amorphization transition at about 600 K, and then transforms at about 700 K to ZIF-zni, the densest of the crystalline ZIFs. This series of long-range structural rearrangements must give a corresponding series of changes in the local structure, but these have not previously been directly investigated. Through analysis of neutron total diffraction data by reverse Monte Carlo modelling, we assess the changes in flexibility across this series, identifying the key modes of flexibility within ZIF-4 and the amorphous phase. We show that the ZnN4 tetrahedra remain relatively rigid, albeit less so than SiO4 tetrahedra in silicates. However, the extra degrees of freedom afforded by the imidazolate ligand, compared to silicate networks, vary substantially between phases, with a twisting motion out of the plane of the ligand being particularly important in the amorphous phase. Our results further demonstrate the feasibility of reverse Monte Carlo simulations for studying intermolecular interactions in solids, even in cases, such as the ZIFs, where the pair distribution function is dominated by intramolecular peaks.