2012
DOI: 10.1007/s10008-012-1716-5
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Investigation of the microstructural features of SrCo0.8Fe0.2O3−δ perovskite

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Cited by 8 publications
(4 citation statements)
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References 23 publications
(36 reference statements)
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“…It is interesting that a similar diffraction pattern (Fig. 10b) was observed previously for the SrCo 0.8 Fe 0.2 O 2.66 sample obtained by slow cooling in air (Belenkaya et al, 2012). In this case, an increase in the oxygen stoichiometry of SrCo 0.8 -Fe 0.2 O 2.5+x is also accompanied by compositional disorder as a result of the formation of non-isovalent B 4+ cations and oxygen excess.…”
Section: Discussionsupporting
confidence: 84%
“…It is interesting that a similar diffraction pattern (Fig. 10b) was observed previously for the SrCo 0.8 Fe 0.2 O 2.66 sample obtained by slow cooling in air (Belenkaya et al, 2012). In this case, an increase in the oxygen stoichiometry of SrCo 0.8 -Fe 0.2 O 2.5+x is also accompanied by compositional disorder as a result of the formation of non-isovalent B 4+ cations and oxygen excess.…”
Section: Discussionsupporting
confidence: 84%
“…7-9). Previously, we have shown 43,44 that this kind of diffraction pattern is associated with nanostructuring of nonstoichiometric doped perovskites: local ordering of oxygen vacancies in 90 nanodomains coherently jointed between themselves and domains with perovskite structure. It results in a coherent lattice where the long-range order is characterized by the perovskite subcell a p whereas the From the viewpoint of theoretical group analysis, the ferroelastic phase transition from the cubic phase P 1 with S.G. Pm 3m (order of group: 48) to tetragonal T phase with S.G. P4/ mmm (order of group: 16) should be accompanied by the formation of three types of 90 domains.…”
Section: 2mentioning
confidence: 85%
“…The difference is due to the separation into two phases (perovskite and brownmillerite) which is known to occur with the formation of immiscible coexisting nanostructured domains of both compositions. 11,16,19,32 On increasing the temperature, the perovskite phase width increases and the miscibility gap narrows. Above 900°C (Figures 2 and 3), the miscibility gap is small and the observed stoichiometry is almost the same on heating and cooling.…”
Section: Resultsmentioning
confidence: 99%
“…In Figure , different values of δ are observed on increasing and decreasing p O 2 at T ≤850°C. The difference is due to the separation into two phases (perovskite and brownmillerite) which is known to occur with the formation of immiscible coexisting nanostructured domains of both compositions . On increasing the temperature, the perovskite phase width increases and the miscibility gap narrows.…”
Section: Discussionmentioning
confidence: 99%