Structure evolution upon chemical and physical pressure in (Sr1−xBax)2FeSbO6

T. Tiittanen, M. Karppinen*

*Corresponding author for this work

Research output: Contribution to journalArticleScientificpeer-review

6 Citations (Scopus)
141 Downloads (Pure)

Abstract

Here we demonstrate the gradual structural transformation from the monoclinic I2/m to tetragonal I4/m, cubic Fm-3m and hexagonal P63/mmc structure upon the isovalent larger-for-smaller A-site cation substitution in the B-site ordered double-perovskite system (Sr1−xBax)2FeSbO6. This is the same transformation sequence previously observed up to Fm-3m upon heating the parent Sr2FeSbO6 phase to high temperatures. High-pressure treatment, on the other hand, transforms the hexagonal P63/mmc structure of the other end member Ba2FeSbO6 back to the cubic Fm-3m structure. Hence we may conclude that chemical pressure, physical pressure and decreasing temperature all work towards the same direction in the (Sr1−xBax)2FeSbO6 system. Also shown is that with increasing Ba-for-Sr substitution level, i.e. with decreasing chemical pressure effect, the degree-of-order among the B-site cations, Fe and Sb, decreases.

Original languageEnglish
Pages (from-to)245-251
Number of pages7
JournalJournal of Solid State Chemistry
Volume246
DOIs
Publication statusPublished - 1 Feb 2017
MoE publication typeA1 Journal article-refereed

Keywords

  • Cation order
  • Chemical pressure
  • Crystal structure
  • Double perovskite
  • High-pressure synthesis

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