Temperature-induced reversible and irreversible transitions between metastable provskite phases in the BiFe1−yScyO3 solid solutions

• Autor(a) principal: Salak, Andrei
• Data de Publicação: 2018
• Outros Autores: Khalyavin, Dmitry, Eardley, Edwin, Olekhnovich, Nikolai, Pushkarev, Anatoli, Radyush, Yury, Shilin, Aleksandr, Rubanik, Vasili
• Tipo de documento: Artigo
• Idioma: eng
• Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
• Texto Completo: http://hdl.handle.net/10773/25403
• topic: Metastable phase; High-pressure synthesis; Perovskite; Polymorphism

The antipolar orthorhombic Pnma phase with the √2ap × 4ap × 2 √2ap superstructure (ap ~4 Å is the pseudocubic perovskite unit-cell parameter) is observed in many perovskite compositions derived from BiFeO3. Temperature-induced structural transformations in metastable perovskite solid solutions with the Pnma structure corresponding to the range of 0.30 ≤ y ≤ 0.60 of the (1−y)BiFeO3 -yBiScO3 quasi binary system were studied using temperature X-ray and neutron powder diffraction. These compositions cannot be prepared in bulk form at ambient pressure but can be stabilized in the Pnma phase by means of quenching after synthesis under high pressure. The compositions were investigated in situ between 1.5 K and the temperature of the stability limit of their metastable phases (about 870–920 K). It has been found that heating the as-preparedp p compositionsp with the Pnma phase leads to formation of the rhombohedral R3c phase (√2ap × √2ap × 2√3ap), which, on cooling downp toproom temperature, either remains or transforms into a polar orthorhombic Ima2 phase (2ap × √2ap × √2ap). The observed phase transformations in the BiFe1−y Scy O3 perovskite series on heating and on cooling are considered in terms of geometrical factors.