Please use this identifier to cite or link to this item: http://hdl.handle.net/10773/36540
Title: Composition-, temperature- and pressure-induced transitions between high-pressure stabilized perovskite phases of the (1-x)BiFe0.5Sc0.5O3 - xLaFe0.5Sc0.5O3 series
Author: Salak, A.N.
Cardoso, J.P.
Khalyavin, D.D.
Barbier, A.
Fertey, P.
Mikhalev, S.M.
Olekhnovich, N.M.
Pushkarev, A.V.
Radyush, Yu V.
Stanulis, A.
Ramanauskas, R.
Keywords: High-pressure synthesis
Metastable perovskite phase
Incommensurate modulation
Issue Date: 25-Feb-2023
Publisher: Elsevier
Abstract: Crystal structures of the high-pressure synthesized perovskite phases of the (1-x)BiFe0.5Sc0.5O3-xLaFe0.5Sc0.5O3 (0 ​= ​x ​≤ ​1) system and their temperature and pressure behaviours were studied using laboratory and synchrotron X-ray diffractions as well as neutron diffraction. At room temperature, the as-prepared phases with x ​≤ ​0.05 have an antipolar structure with the Pnma symmetry and with the √2ap ​× ​4ap ​× ​2√2ap superstructure (where ap is the pseudocubic perovskite unit-cell parameter). An incommensurately modulated phase with the Imma(00γ)s00 superspace group is observed for 0.10 ​= ​x ​≤ ​0.33, while a non-polar Pnma phase (√2ap ​× ​2ap ​× ​√2ap) is stable when x ​≥ ​0.34. The antipolar Pnma phase in the as-prepared samples with composition corresponding to x ​= ​0 transforms into the polar Ima2 one via irreversible annealing-caused transformation accompanied by a formation of a high-temperature intermediate polar R3c polymorph, while the antipolar Pnma phase in samples with x ​= ​0.05 is stable until the decomposition temperature. In the solid solutions with 0.10 ​= ​x ​≤ ​0.33, increasing temperature was found to result in a reversible transformation of the Imma(00γ)s00 phase into a non-polar Pnma one. The transition temperature decreases with increasing x. A hydrostatic pressure of few GPa was also shown to induce a reversible Imma(00γ)s00 → Pnma transformation.
Peer review: yes
URI: http://hdl.handle.net/10773/36540
DOI: 10.1016/j.jssc.2023.123937
ISSN: 0022-4596
Appears in Collections:CICECO - Artigos

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