Zircon to scheelite phase transition induced by pressure and magnetism in TbCrO4

被引:15
|
作者
Climent Pascual, E. [1 ]
Gallardo Amores, J. M. [1 ]
Saez Puche, R. [1 ]
Castro, M. [2 ]
Taira, N. [3 ]
Romero de Paz, J. [4 ]
Chapon, L. C. [5 ]
机构
[1] Univ Complutense Madrid, Fac Ciencias Quim, Dept Quim Inorgan 1, E-28040 Madrid, Spain
[2] Univ Zaragoza, CSIC, Inst Ciencia Mat Aragon, E-50009 Zaragoza, Spain
[3] Gunma Coll Technol, Dept Chem, Gunma 3718530, Japan
[4] Univ Complutense Madrid, Fac Ciencias Fis, CAI Tecn Fis, E-28040 Madrid, Spain
[5] Rutherford Appleton Lab, ISIS Facil, CCLRC, Didcot OX11 0QX, Oxon, England
关键词
X-RAY;
D O I
10.1103/PhysRevB.81.174419
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The scheelite form of the TbCrO4 oxide has been obtained by treating TbCrO4-zircon at 4 GPa and 823 K. X-ray and neutron diffraction data reveal that the high-pressure polymorph of TbCrO4 crystallizes with tetragonal symmetry space group I4(1)/a and lattice parameters a=5.036 74(10) angstrom and c=11.3734(4) angstrom. Although bisdisphenoids [TbO8] and tetrahedra [CrO4] are present in both scheelite and zircon polymorphs, the remarkable changes observed in both polyhedra appear to support the reconstructive model for the zircon-scheelite first-order phase transition. Specific heat and neutron diffraction measurements confirm the antiferromagnetic ordering previously proposed from magnetic susceptibility measurements, in which both Tb3+ and Cr5+ sub-lattices are involved. The magnetic structure has been determined and can be described on the basis of the coincidence between the chemical and magnetic cells, k=(0,0,0), where the magnetic moments of the Tb3+ and Cr5+ cations are antiferromagnetically aligned along the c axis of the structure, with T-N=29 K. Their values at 2 K are 8.97(3)mu(B) and 1.089(9)mu(B), respectively.
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页数:7
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