Loading…
The novel phase transition of NaBi(WO4)2 under high pressure
The Raman and synchrotron angle-dispersive X-ray diffraction studies have been performed on NaBi(WO4)2 under high pressure up to 30.7 and 36.2GPa, respectively, at room temperature. With pressure increases to ∼7.0GPa, the structure of NaBi(WO4)2 begins to transform from tetragonal (I41/a) into monoc...
Saved in:
Published in: | Journal of solid state chemistry 2013-04, Vol.200, p.246-250 |
---|---|
Main Authors: | , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Summary: | The Raman and synchrotron angle-dispersive X-ray diffraction studies have been performed on NaBi(WO4)2 under high pressure up to 30.7 and 36.2GPa, respectively, at room temperature. With pressure increases to ∼7.0GPa, the structure of NaBi(WO4)2 begins to transform from tetragonal (I41/a) into monoclinic (P2/m), and the phase transition completes around 13GPa. With pressure higher than 29.0GPa, the NaBi(WO4)2 turns into amorphous state. The random arrangement of Na+ and Bi3+ in short-range ordered scheelite NaBi(WO4)2 results in the tetragonal to monoclinic phase transition, which is different from that observed in AWO4 tungstates and AMoO4 molybdates (A=Ca, Sr, Ba, Pb, Eu, Cd).
The NaBi(WO4)2 transforms from tetragonal into monoclinic, which starts around 7GPa and completes at about 13GPa. With pressure higher than 29GPa, the NaBi(WO4)2 turns into amorphous state. [Display omitted]
► Raman and X-ray diffraction studies performed on NaBi(WO4)2 up to 30.7 and 36.2GPa, respectively. ► The tetragonal (I41/a) into monoclinic (P2/m) phase transition is determined. ► With pressure higher than 29GPa, the NaBi(WO4)2 ultimately turns into amorphous state. ► The ambient pressure bulk modulus and volume of tetragonal and monoclinic phases are obtained. |
---|---|
ISSN: | 0022-4596 1095-726X |
DOI: | 10.1016/j.jssc.2013.01.049 |