We prepared trirutile-type polycrystalline samples of CuTaO 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 CuTaO 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.
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http://dx.doi.org/10.1021/acs.inorgchem.7b00421 | DOI Listing |
J Fluoresc
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Electrical Engineering, Indian Institute of Technology, Gandhinagar, Gujarat, India.
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Physical Chemistry Department, National Research Centre, 33 El Bohouth Street, P.O.12622, Dokki, Giza, Egypt.
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Swinburne University of Technology - Hawthorn Campus: Swinburne University of Technology, Chemistry and Biotechnology, AUSTRALIA.
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