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水热合成 BaTiO 纳米晶中四方结构的稳定机制。

Stabilization Mechanism of the Tetragonal Structure in a Hydrothermally Synthesized BaTiO Nanocrystal.

机构信息

National Institute for Materials Science , 1-2-1 Sengen , Tsukuba, Ibaraki 305-0047 , Japan.

Computational Engineering Applications Unit , RIKEN , 2-1 Hirosawa , Wako, Saitama 351-0198 , Japan.

出版信息

Inorg Chem. 2018 May 7;57(9):5413-5419. doi: 10.1021/acs.inorgchem.8b00381. Epub 2018 Apr 16.

Abstract

Higher OH concentration is identified in tetragonal barium titanate (BaTiO) nanorods synthesized by a hydrothermal method with a 10 vol % ethylene glycol solvent (Inada, M.; et al. Ceram. Int. 2015, 41, 5581-5587). This is apparently inconsistent with the known fact that higher OH concentration in the conventional hydrothermal synthesis makes pseudocubic BaTiO nanocrystals more stable than the tetragonal one. To understand where and how the introduced OH anions are located and behave in the nanocrystals, we applied ab initio analysis to several possible microscopic geometries of OH locations, confirming the relative stability of the tetragonal distortion over the pseudocubic one because of the preference of trans-type configurations of OH anions. We also performed Fourier transform infrared and X-ray diffraction analysis, all being consistent with the microscopic picture established by the ab initio geometrical optimizations.

摘要

在水热法中使用 10 体积%的乙二醇溶剂合成的四方相钛酸钡(BaTiO)纳米棒中,OH 浓度更高(Inada,M.等人,《陶瓷国际》,2015 年,第 41 卷,第 5581-5587 页)。这显然与一个已知事实相矛盾,即常规水热合成中更高的 OH 浓度使得伪立方 BaTiO 纳米晶比四方相更稳定。为了了解引入的 OH 阴离子在纳米晶中位于何处以及如何表现,我们对几种可能的 OH 位置的微观几何结构进行了从头算分析,证实了由于 OH 阴离子的反式构型的偏好,四方相畸变相对于伪立方相更稳定。我们还进行了傅里叶变换红外和 X 射线衍射分析,所有这些都与由从头算几何优化建立的微观图像一致。

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