Effect of Hydrothermal Treatment and Doping on the Microstructural Features of Sol-Gel Derived BaTiO3 Nanoparticles

材料科学 钛酸钡 结晶度 四方晶系 掺杂剂 纳米颗粒 溶胶凝胶 化学工程 兴奋剂 热液循环 纳米复合材料 相(物质) 微观结构 扫描电子显微镜 煅烧 纳米技术 水热合成 分析化学(期刊) 锐钛矿 矿物学 核化学 傅里叶变换红外光谱 透射电子显微镜 粒径 比表面积 微晶
作者
Nico Zamperlin,Riccardo Ceccato,Marco Fontana,Alessandro Pegoretti,Andrea Chiappini,Sandra Dirè
出处
期刊:Materials [MDPI AG]
卷期号:14 (15): 4345-4345
标识
DOI:10.3390/ma14154345
摘要

Barium Titanate (BaTiO3) is one of the most promising lead-free ferroelectric materials for the development of piezoelectric nanocomposites for nanogenerators and sensors. The miniaturization of electronic devices is pushing researchers to produce nanometric-sized particles to be embedded into flexible polymeric matrices. Here, we present the sol-gel preparation of crystalline BaTiO3 nanoparticles (NPs) obtained by reacting barium acetate (Ba(CH3COO)2) and titanium (IV) isopropoxide (Ti(OiPr)4). The reaction was performed both at ambient conditions and by a hydrothermal process carried on at 200 °C for times ranging from 2 to 8 h. Doped BaTiO3 nanoparticles were also produced by addition of Na, Ca, and Bi cations. The powders were annealed at 900 °C in order to improve NPs crystallinity and promote the cubic-to-tetragonal (c⟶t) phase transformation. The microstructural features of nanoparticles were investigated in dependence of both the hydrothermal reaction time and the presence of dopants. It is found that short hydrothermal treatment (2 h) can produce BaTiO3 spherical and more homogeneous nanoparticles with respect to longer hydrothermal treatments (4 h, 6 h, 8 h). These particles (2 h) are characterized by decreased dimension (approx. 120 nm), narrower size distribution and higher tetragonality (1.007) in comparison with particles prepared at ambient pressure (1.003). In addition, the short hydrothermal treatment (2 h) produces particles with tetragonality comparable to the one obtained after the longest process (8 h). Finally, dopants were found to affect to different extents both the c⟶t phase transformation and the crystallite sizes.
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