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Author Habu, Daiki ♦ Masubuchi, Yuji ♦ Torii, Shuki ♦ Kamiyama, Takashi ♦ Kikkawa, Shinichi
Source United States Department of Energy Office of Scientific and Technical Information
Content type Text
Language English
Subject Keyword INORGANIC, ORGANIC, PHYSICAL AND ANALYTICAL CHEMISTRY ♦ ANIONS ♦ COMPARATIVE EVALUATIONS ♦ CRYSTAL STRUCTURE ♦ CRYSTALS ♦ DIELECTRIC MATERIALS ♦ LANTHANUM COMPLEXES ♦ MIXING ♦ MIXING RATIO ♦ NITRIDES ♦ PARAFFIN ♦ PERMITTIVITY ♦ PEROVSKITE ♦ POWDERS ♦ STRONTIUM COMPLEXES ♦ TITANIUM OXIDES
Abstract As is the case with SrTaO{sub 2}N, both cis-ordering of nitride anions and octahedral titling are also preferable in La{sub 1−x}Sr{sub x}TiO{sub 2+x}N{sub 1−x} (x=0, 0.2) oxynitride perovskites. A larger dielectric constant of ε{sub r}≈5.0×10{sup 3} was estimated for the pure oxynitride with x=0.2, compared with ε{sub r}≈750 for the product with x=0, by extrapolating the ε{sub r} values obtained from powders mixed with paraffin at various mixing ratios. The crystal structure of x=0.2 with larger tolerance factor than x=0 increased the octahedral tilting, which contributes to the increased dielectric constant. The increased dielectric constant supports the exchange mechanism for the dielectric property between two kinds of –Ti–N– helical coils (clockwise and anticlockwise) derived from the above cis-ordering of nitride anions. - Graphical abstract: Very large dielectric constant values were estimated for La{sub 1−x}Sr{sub x}TiO{sub 2+x}N{sub 1−x}; ε{sub r}≈5.0×10{sup 3} in x=0.2 and ε{sub r}≈750 in x=0. - Highlights: • Cis-configuration of nitride anions was confirmed in La{sub 1−x}Sr{sub x}TiO{sub 2+x}N{sub 1−x} (x=0, 0.2). • Dielectric constant values were estimated to be 750 for x=0 and 5.0×10{sup 3} for x=0.2, respectively. • The large dielectric property is to the exchange mechanism between clockwise and anticlockwise –Ti–N– coil motifs.
ISSN 00224596
Educational Use Research
Learning Resource Type Article
Publisher Date 2016-05-15
Publisher Place United States
Journal Journal of Solid State Chemistry
Volume Number 237


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