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氮氧化合物钙钛矿 SrTaON 与拉多姆斯登-波普相 SrTaON 之间的共生关系。

Intergrowth between the Oxynitride Perovskite SrTaON and the Ruddlesden-Popper Phase SrTaON.

机构信息

Faculty of Engineering , Hokkaido University , N13W8 , Sapporo 060-8628 , Japan.

TDK Corporation, Technology & Intellectual Property HQ , 2-15-7 Higashi-Ohwada , Ichikawa , Chiba 272-8558 , Japan.

出版信息

Inorg Chem. 2018 Aug 6;57(15):9086-9095. doi: 10.1021/acs.inorgchem.8b01079. Epub 2018 Jul 16.

Abstract

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 SrTaON and the Ruddlesden-Popper phase SrTaON with increasing SrO content. X-ray diffraction analyses showed that a single-phase perovskite was obtained up to x = 1.1, after which SrTaON gradually appeared at x ≥ 1.25. High-resolution scanning transmission electron microscopy observations identified the gradual intergrowth of a Ruddlesden-Popper SrTaON 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 SrTaON. Characterization of SrTaON 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 SrTaON perovskite, especially under nitrogen. SrTaON 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 SrTaON perovskite under these same conditions. Postammonolysis of the SrTaON ceramics was not required prior to studying its dielectric behavior. This is in contrast to the SrTaON perovskite, which requires postammonolysis to recover its stoichiometric composition and electrical insulating properties.

摘要

锶钽氧氮化物在名义组成范围内 1.0≤x≤2.0 范围内进行制备,其中 x=Sr/Ta 原子比。随着 SrO 含量的增加,观察到钙钛矿 SrTaON 与 Ruddlesden-Popper 相 SrTaON 之间存在结构的逐渐转变。X 射线衍射分析表明,在 x=1.1 之前,仅获得单相钙钛矿,之后在 x≥1.25 时 SrTaON 逐渐出现。高分辨率扫描透射电子显微镜观察确定,随着 x 的增加,Ruddlesden-Popper SrTaON 型平面结构逐渐交织在钙钛矿晶格中。在 x=1.4 时,晶格高度缺陷,主要由与大量 Ruddlesden-Popper 相结构共生长的钙钛矿组成。这种 Ruddlesden-Popper 相层交织是氮氧化物钙钛矿的特征,而不是先前在氧化物钙钛矿中报道的 Ruddlesden-Popper 缺陷。在这种钙钛矿晶格中也可以明显看出 Ta 被 Sr 的部分取代。在 x=2 以下,在 Ruddlesden-Popper SrTaON 中,钙钛矿型结构作为缺陷共生长。在大气条件下对 SrTaON 的特性进行表征具有挑战性,因为它对水分敏感。热分析表明,与 SrTaON 钙钛矿相比,在氮气中,该材料在 1400°C 以下相对稳定,特别是在氮气中。在先前的大气条件下,将该材料暴露于 75%相对湿度下 10 天后,在 XRD 中观察到一些 SrCO。在 1400°C 下,在 0.2 MPa 的氮气中烧结后,该材料的致密块体具有 96%的相对密度,尽管先前在相同条件下报道 SrTaON 钙钛矿存在严重的氮损失。在研究其介电性能之前,不需要对 SrTaON 陶瓷进行后氨解。这与 SrTaON 钙钛矿形成对比,SrTaON 钙钛矿需要后氨解才能恢复其化学计量组成和电绝缘性能。

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