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RESEARCH PRODUCT
In-situ high-pressure Raman scattering studies in PbWO4 up to 48 GPa
Daniel ErrandoneaAlain PolianAlain PolianK. K. MishraR. Lacomba-peralessubject
Phase transitionMaterials scienceAnalytical chemistryFOS: Physical sciences02 engineering and technology01 natural scienceschemistry.chemical_compoundTetragonal crystal systemsymbols.namesakePhase (matter)0103 physical sciencesMaterials Chemistry010306 general physics[PHYS]Physics [physics]Condensed Matter - Materials ScienceMechanical EngineeringMetals and AlloysMaterials Science (cond-mat.mtrl-sci)021001 nanoscience & nanotechnologyHigh pressureCrystallographychemistryPhase transitionsMechanics of MaterialsScheeliteRaman spectroscopysymbols0210 nano-technologyRaman spectroscopyRaman scatteringAmbient pressureMonoclinic crystal systemdescription
The effect of pressure on the Raman spectrum of PbWO4 has been investigated up to 48 GPa in a diamond-anvil cell using neon as pressure-transmitting medium. Changes are detected in the Raman spectrum at 6.8 GPa as a consequence of a structural phase transition from the tetragonal scheelite structure to the monoclinic PbWO4-III structure. Two additional phase transitions are detected at 15.5 and 21.2 GPa to the previously unknown crystalline phases IV and V. The last one remains stable up to 43.3 GPa. At 47.7 GPa all Raman modes disappear, which could be caused by a pressure-induced amorphization. All structural changes are reversible, being the scheelite phase recovered at ambient pressure. However, the two most intense modes of the PbWO4-III phase are still present after full decompression, indicating that this phase coexists as a minority metastable phase with the scheelite phase after pressure release. The wavenumber of the Raman modes and their pressure dependencies are reported for the four crystalline phases. The present reported results are compared with previous studies.
year | journal | country | edition | language |
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2016-01-01 | Journal of Alloys and Compounds |