6533b827fe1ef96bd12866a6

RESEARCH PRODUCT

PrVO$_4$ under High Pressure: Effects on Structural, Optical and Electrical Properties

Marco BettinelliEnrico BandielloDaniel ErrandoneaJuan Angel SansCatalin PopescuEstelina Lora Da SilvaEstelina Lora Da Silva

subject

Work (thermodynamics)Condensed Matter - Materials Science010405 organic chemistryChemistryMaterials Science (cond-mat.mtrl-sci)FOS: Physical sciences010402 general chemistryCompression (physics)01 natural sciences0104 chemical sciencesCharacterization (materials science)Inorganic ChemistryCondensed Matter - Other Condensed MatterHigh pressurePhase (matter)Physical and Theoretical ChemistryComposite materialOther Condensed Matter (cond-mat.other)

description

In pursue of a systematic characterization of rare-earth vanadates under compression, in this work we present a multifaceted study of the phase behavior of zircon-type orthovanadate PrVO$_4$ under high pressure conditions, up until 24 GPa. We have found that PrVO$_4$ undergoes a zircon to monazite transition at around 6 GPa, confirming previous results found by Raman experiments. A second transition takes place above 14 GPa, to a BaWO$_4$-I--type structure. The zircon to monazite structural sequence is an irreversible first-order transition, accompanied by a volume collapse of about 9.6%. Monazite phase is thus a metastable polymorph of PrVO$_4$. The monazite-BaWO$_4$-II transition is found to be reversible instead and occurs with a similar volume change. Here we report and discuss the axial and bulk compressibility of all phases. We also compare our results with those for other rare-earth orthovanadates. Finally, by means of optical-absorption experiments and resistivity measurements we determined the effect of pressure on the electronic properties of PrVO$_4$. We found that the zircon-monazite transition produces a collapse of the band gap and an abrupt decrease of the resistivity. The physical reasons for this behavior are discussed. Density-functional-theory simulations support our conclusions.

10.1021/acs.inorgchem.0c02933http://arxiv.org/abs/2006.01299