Polymorphism of praseodymium orthovanadate under high pressure

被引:10
作者
Marqueno, T. [1 ]
Errandonea, D. [1 ]
Pellicer-Porres, J. [1 ]
Santamaria-Perez, D. [1 ]
Martinez-Garcia, D. [1 ]
Bandiello, E. [1 ]
Rodriguez-Hernandez, P. [2 ]
Munoz, A. [2 ]
Achary, S. N. [3 ]
Popescu, C. [4 ]
机构
[1] Univ Valencia, Dept Fis Aplicada ICMUV, Dr Moliner 50, Valencia 46100, Spain
[2] Univ La Laguna, Inst Mat & Nanotecnol, Dept Fis, Tenerife 38200, Spain
[3] Bhabha Atom Res Ctr, Chem Div, Mumbai 400085, Maharashtra, India
[4] CELLS ALBA Synchrotron Light Facil, Barcelona 08290, Spain
关键词
X-RAY-DIFFRACTION; CRYSTAL-STRUCTURE; TRANSFORMATIONS; REFINEMENTS; STABILITY; PROGRAM; PRVO4; PR; ND; CE;
D O I
10.1103/PhysRevB.103.134113
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Zircon-type PrVO4 has been studied at high pressures and room temperature by means of synchrotron powder x-ray diffraction. At room temperature, we observed the previously known zircon-to-monazite phase transition at 5.5(4) GPa and a second phase transition from monazite to a monoclinic structure at 12.7(8) GPa, which we identified as a PbWO4 -III-type phase. This conclusion is supported by our ab initio calculations, which also predict a scheelite-type phase to be stable at high pressure. Motivated by this finding, we subjected zircon-type PrVO4 samples to high pressure (7 GPa) and temperature (600, 800, and 1000 degrees C) in a Paris-Edinburgh large volume press cell. As a result, we could synthesize a scheelite-type phase of PrVO4, which was recovered in a metastable state at room conditions, and the unit-cell parameters and the atomic positions have been determined. We also report a substantial increase of the scheelite proportion with time by comparing synthesis of different durations, at the same pressure-temperature conditions. The transition mechanisms of the zircon-, monazite-, and scheelite-type structures as well as the role of kinetic barriers will be discussed. Information on the compressibility of different polymorphs will be reported too.
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页数:11
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