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Intergrowth between the Oxynitride Perovskite SrTaO 2 N and the Ruddlesden-Popper Phase Sr 2 TaO 3 N

Strontium tantalum oxynitrides were prepared within the nominal composition range of 1.0 ≤ x ≤ 2.0, where x = Sr/Ta atomic ratio. A gradual structural transition was observed between the perovskite SrTaO N and the Ruddlesden-Popper phase Sr TaO N with increasing SrO content. X-ray diffraction analys...

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Bibliographic Details
Published in:Inorganic chemistry 2018-08, Vol.57 (15), p.9086-9095
Main Authors: Suemoto, Yuya, Masubuchi, Yuji, Nagamine, Yuki, Matsutani, Atsuo, Shibahara, Takeshi, Yamazaki, Kumiko, Kikkawa, Shinichi
Format: Article
Language:English
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Summary:Strontium tantalum oxynitrides were prepared within the nominal composition range of 1.0 ≤ x ≤ 2.0, where x = Sr/Ta atomic ratio. A gradual structural transition was observed between the perovskite SrTaO N and the Ruddlesden-Popper phase Sr TaO N with increasing SrO content. X-ray diffraction analyses showed that a single-phase perovskite was obtained up to x = 1.1, after which Sr TaO N gradually appeared at x ≥ 1.25. High-resolution scanning transmission electron microscopy observations identified the gradual intergrowth of a Ruddlesden-Popper Sr TaO N type planar structure interwoven with the perovskite crystal lattice upon increasing x. The crystal lattice at x = 1.4 was highly defective and consisted primarily of perovskite intergrown with a large amount of the Ruddlesden-Popper phase structure. This Ruddlesden-Popper phase layer intergrowth is a characteristic of an oxynitride perovskite rather than the Ruddlesden-Popper defects previously reported in oxide perovskites. Partial substitution of Ta with Sr was also evident in this perovskite lattice. Just below x = 2, a perovskite-type structure was intergrown as defects in the Ruddlesden-Popper Sr TaO N. Characterization of Sr TaO N in ambient air was challenging due to its moisture sensitivity. Thermal analysis demonstrated that this material was relatively stable up to approximately 1400 °C in comparison with SrTaO N perovskite, especially under nitrogen. Sr TaO N could keep its structure in a sealed tube, and some amount of SrCO was observed in XRD after 10 days of exposure to 75% relative humidity under prior ambient conditions. A compact of this material had a relative density of 96% after sintering at 1400 °C under 0.2 MPa of nitrogen, even though a drastic loss of nitrogen was previously reported for a SrTaO N perovskite under these same conditions. Postammonolysis of the Sr TaO N ceramics was not required prior to studying its dielectric behavior. This is in contrast to the SrTaO N perovskite, which requires postammonolysis to recover its stoichiometric composition and electrical insulating properties.
ISSN:0020-1669
1520-510X
DOI:10.1021/acs.inorgchem.8b01079