Ferroelectricity in d0 double perovskite fluoroscandates

Nenian Charles, James M. Rondinelli

Research output: Contribution to journalArticlepeer-review

1 Scopus citations

Abstract

Ferroelectricity in strain-free and strained double perovskite fluorides, Na3ScF6 and K2NaScF6, is investigated using first-principles density functional theory. Although the experimental room temperature crystal structures of these fluoroscandates are centrosymmetric, i.e., Na3ScF6 (P21/n) and K2NaScF6 (Fm3¯m), lattice dynamical calculations reveal that soft polar instabilities exist in each prototypical cubic phase and that the modes harden as the tolerance factor approaches unity. Thus the double fluoroperovskites bear some similarities to ABO3 perovskite oxides; however, in contrast, these fluorides exhibit large acentric displacements of alkali metal cations (Na, K) rather than polar displacements of the transition metal cations. Biaxial strain investigations of the centrosymmetric and polar Na3ScF6 and K2NaScF6 phases reveal that the paraelectric structures are favored under compressive strain, whereas polar structures with in-plane electric polarizations (∼5-18μCcm-2) are realized at sufficiently large tensile strains. The electric polarization and stability of the polar structures for both chemistries are found to be further enhanced and stabilized by a coexisting single octahedral tilt system. Our results suggest that polar double perovskite fluorides may be realized by suppression of octahedral rotations about more than one Cartesian axis; structures exhibiting in- or out-of-phase octahedral rotations about the c axis are more susceptible to polar symmetries.

Original languageEnglish (US)
Article number054111
JournalPhysical Review B - Condensed Matter and Materials Physics
Volume92
Issue number5
DOIs
StatePublished - Aug 27 2015

ASJC Scopus subject areas

  • Electronic, Optical and Magnetic Materials
  • Condensed Matter Physics

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