四方晶系
微晶
材料科学
拉曼光谱
热液循环
晶格常数
水热合成
分析化学(期刊)
晶体结构
大气温度范围
相(物质)
纳米颗粒
结晶学
相变
矿物学
衍射
化学工程
纳米技术
化学
冶金
光学
凝聚态物理
色谱法
气象学
工程类
物理
有机化学
作者
Hiromichi Hayashi,Takeo Ebina
出处
期刊:Nippon Seramikkusu Kyōkai gakujutsu rombunshi
[Ceramic Society of Japan]
日期:2018-01-01
卷期号:126 (3): 214-220
被引量:14
标识
DOI:10.2109/jcersj2.17125
摘要
Highly crystalline BaTiO3 particles were hydrothermally synthesized at 250–400°C from the reactants of TiO2 sol and Ba(OH)2 solution. X-ray diffraction measurement patterns revealed that the crystal phase of the obtained particles was tetragonal, whereas tetragonality (c/a) was difficult to estimate due to the peak broadening of BaTiO3 nanoparticles. The particle sizes determined based on the BET surface area and crystallite sizes were almost constant at 80 and 40 nm, irrespective of the hydrothermal temperature. Based on TG–DTA analyses, the lattice OH content decreased with increases in the hydrothermal temperature. In-situ Raman spectra were conducted in the temperature range from 25 to 200°C to follow the tetragonal-to-cubic transformation. The tetragonal-to-cubic phase transition was clearly observed at 120–130°C for the BaTiO3 hydrothermally synthesized at 400°C, whereas the BaTiO3 hydrothermally synthesized at 250–350°C exhibited a delayed transition at above 150°C due to peudo-cubic behavior. The tetragonality of BaTiO3 synthesized at 400°C can be assumed to be prominent owing to the lower number of lattice OH groups.
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