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微波辅助半溶剂热法合成纳米晶钛酸钡

Microwave assisted semi-solvothermal synthesis of nanocrystalline barium titanate.

作者信息

Lee Jong-Min, Amalnerkar Dinesh P, Hwang Young Kyu, Jhung Sung Hwa, Hwang Jin-Soo, Chang Jong-San

机构信息

Research Center for Nanocatalysts, Korea Research Institute of Chemical Technology, PO. Box 107, Yuseong, Daejeon 305-343, Korea.

出版信息

J Nanosci Nanotechnol. 2007 Mar;7(3):952-9. doi: 10.1166/jnn.2007.403.

Abstract

In an endeavor to synthesize tetragonal nanocrystallites of BaTiO3 at much reduced reaction time, we explored the possibility of performing microwave assisted semi-solvothermal reaction by using Ba(OH)2 . 8H2O and amorphous titanium hydrous gel as precursors and 1,4-butanediol and water as solvent. Typically, such a microwave assisted reaction was accomplished within 2 hrs at 220 degrees C as against 12 hrs required in conventional approach. The crystallized BaTiO3 powders (microwave assisted as well as conventionally processed for reference) were characterized by X-ray diffraction, thermal analysis, infrared spectroscopy, Raman spectroscopy, scanning electron microscopy, transmission electron microscopy, and atomic force microscopy. We have detected metastable cubic phase by XRD while locally symmetric tetragonal phase by Raman spectroscopy in case of conventional semi-solvothermal processing. On the contrary, we could detect co-existence of tetragonal and cubic phases by XRD and only tetragonal phase by Raman spectroscopy in case of microwave assisted semi-solvothermal processing. The TEM analysis indicates typical particle size distribution in the range of approximately 20 to 80 nm for conventionally processed powder while that in the range of approximately 20 to 50 nm for microwave processed powder. HRTEM images evince the distortion from an ideal cubic structure in case of microwave processed powder which can be correlated with anisotropic lattice contraction during the microwave induced heating. AFM analysis exhibited relatively less aggregation of nanoparticles for microwave assisted process.

摘要

为了在大幅缩短反应时间的情况下合成四方晶型的钛酸钡纳米微晶,我们探索了使用Ba(OH)₂·8H₂O和无定形含水钛凝胶作为前驱体,1,4 - 丁二醇和水作为溶剂进行微波辅助半溶剂热反应的可能性。通常,这种微波辅助反应在220℃下2小时内即可完成,而传统方法则需要12小时。通过X射线衍射、热分析、红外光谱、拉曼光谱、扫描电子显微镜、透射电子显微镜和原子力显微镜对结晶的钛酸钡粉末(微波辅助以及传统方法制备作为参考)进行了表征。在传统半溶剂热法中,通过XRD检测到亚稳立方相,通过拉曼光谱检测到局部对称的四方相。相反,在微波辅助半溶剂热法中,通过XRD可以检测到四方相和立方相共存,通过拉曼光谱仅检测到四方相。TEM分析表明,传统方法制备的粉末的典型粒径分布在约20至80nm范围内,而微波处理的粉末的粒径分布在约20至50nm范围内。HRTEM图像显示,微波处理的粉末偏离了理想的立方结构,这与微波诱导加热过程中的各向异性晶格收缩有关。AFM分析表明,微波辅助过程中纳米颗粒的聚集相对较少。

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