Structural and Magnetic Properties of the Trirutile-type 1D-Heisenberg Anti-Ferromagnet CuTa2O6.
Aleksandr GolubevRobert E DinnebierArmin SchulzReinhard K KremerHubert LangbeinAnatoliy SenyshynJoseph M LawThomas C HansenHyun-Joo KooMyung-Hwan WhangboPublished in: Inorganic chemistry (2017)
We prepared trirutile-type polycrystalline samples of CuTa2O6 by low-temperature decomposition of a Cu-Ta-oxalate precursor. Diffraction studies at room temperature identified a slight monoclinic distortion of the hitherto surmised tetragonal trirutile crystal structure. Detailed high-temperature X-ray and neutron powder diffraction investigations as well as Raman scattering spectroscopy revealed a structural phase transition at 503(3) K from the monoclinic structure to the tetragonal trirutile structure. GGA+U density functional calculations of the spin-exchange parameters as well as magnetic susceptibility and isothermal magnetization measurements reveal that CuTa2O6 is a new 1D Heisenberg magnet with predominant anti-ferromagnetic nearest-neighbor intrachain spin-exchange interaction of ∼50 K. Interchain exchange is a factor of ∼5 smaller. Heat capacity and low-temperature high-intensity neutron powder diffraction studies could not detect long-range order down to 0.45 K.
Keyphrases
- room temperature
- crystal structure
- high intensity
- high temperature
- ionic liquid
- high resolution
- molecularly imprinted
- resistance training
- case control
- single cell
- density functional theory
- electron microscopy
- single molecule
- molecular dynamics
- genome wide
- heat stress
- molecular dynamics simulations
- monte carlo
- mass spectrometry
- label free
- liquid chromatography
- nucleic acid
- aqueous solution
- tandem mass spectrometry