首页|基于异丙醇溶剂热合成四方相BaTiO3工艺探索及机理研究

基于异丙醇溶剂热合成四方相BaTiO3工艺探索及机理研究

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以Ba(OH)2·8H2O和Ti(OC4H9)4 为原料、异丙醇(IPA)为溶剂,通过溶剂热法合成富四方相纳米钛酸钡(BTO)粉体,研究了钡钛比、体系pH值、溶剂热温度及时间等因素对制备高四方性纳米BTO粉体的影响,利用X射线衍射和扫描电镜等表征方法研究了IPA在溶剂热制备BTO过程中的作用机理.结果表明,溶剂热工艺合成过程中,IPA会优先提供一定的—OH以促进Ti(OC4H9)4的水解,生成TiO6 八面体并与Ba2+连接.在低碱度环境中,经相转变、小颗粒溶解与重结晶等过程逐步转变为形貌规整的四方相BTO.钡钛比1.6、体系pH值10、溶剂热温度220℃、时间24 h、煅烧温度950℃、煅烧时间2h时制备的富四方相纳米BTO粉体分散均匀、形貌规整,呈四方形或近四方形,c/a值达1.0094,平均粒径为124 nm.
Exploration into Synthesis of Tetragonal Phase BaTiO3 Based on Isopropanol Solvothermal Process and Its Mechanism
With Ba(OH)2·8H2O and Ti(OC4H9)4 as raw materials,and isopropanol(IPA)as solvent,tetragonal-rich BaTiO3(BTO)nanopowder was synthesized by adopting solvothermal process.Effects of Ba/Ti ratio,pH value,solvothermal temperature and time on synthesis of tetragonal-rich BTO powders were investigated,and the mechanism of IPA in the solvothermal process for synthesis of BTO powders was also characterized by X-ray diffraction and scanning electron microscopy.It is found that in the solvothermal process,IPA will preferentially provide certain—OH to promote the hydrolysis of Ti(OC4H9)4,generating TiO6 octahedra to interconnect with Ba2+,which is gradually transformed into the tetragonal phase BaTiO3 with regular morphology after phase transition,dissolution of small particles,and recrystallization in a low alkalinity environment.Experimental results show that under the following conditions including Ba/Ti ratio of 1.6,pH of 10 for the system,a solvothermal process at 220℃for 24 h,calcination at 950℃for 2 h,the synthesized tetragonal-rich BTO nanopowder is well dispersed with regular morphology,square or nearly square shape,with c/a value of 1.0094 and particle size of 124 nm on average.

barium titanatetetragonal phaseisopropanol(IPA)solvothermal processceramic capacitorsperovskite materialssynthesis

盖卉妍、戴超华、杨林

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长沙矿冶研究院有限责任公司,湖南长沙 410012

长沙矿冶院检测技术有限责任公司,湖南长沙 410012

钛酸钡 四方相 异丙醇(IPA) 溶剂热法 陶瓷电容器 钙钛矿材料 合成制备

2024

矿冶工程
长沙矿冶研究院有限责任公司 中国金属学会

矿冶工程

CSTPCD北大核心
影响因子:1.137
ISSN:0253-6099
年,卷(期):2024.44(2)
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