期刊文献+

熔盐法由BaO2·H2O2合成BaTiO3纳米粒子及其表征 被引量:2

Synthesis and characterization of BaTiO_3 nanoparticles from BaO_2·H_2O_2 by molten salt method
在线阅读 下载PDF
导出
摘要 将BaCl2.2H2O和H2O2溶液在NH3.H2O中反应制备出前驱体BaO2.H2O2,再用H2TiO3和前驱体BaO2.H2O2作反应物、KNO3和KOH作溶剂,用熔盐法合成了钛酸钡纳米粒子,用XRD、SEM、TEM、EDS和FT-IR对产品的结构、形貌和成份进行了表征。结果表明,在500~600℃煅烧24h可获得粒径约为25~50nm的立方相钛酸钡纳米粒子,粒子大小分布均匀,形状近似为球形。随着反应温度升高,BaTiO3纳米粒子的晶胞参数减少、粒径增大。另外,还讨论了BaTiO3纳米粒子的形成机理。 The precursor,BaO2·H2O2 were prepared from the reaction of BaCl2·2H2O and H2O2 in NH3·H2O aqueous solution under the ambient condition.BaTiO3 nanoparticles were produced by molten salt method using H2TiO3 and the as-prepared precursor BaO2·H2O2 as reactant,KNO3 and KOH as a flux.XRD,SEM,TEM,EDS and FT-IR techniques were used to characterize the structures,morphologies and compositions of the products.The results show that BaTiO3 nanoparticles with uniform size distribution and particle sizes of 25-50nm,similar to spherical shape,can be obtained through calcining an mixture of the molten salt at 500-600℃ for 24h,and the structures of the as-obtained nanoparticles are of cubic phases.As the increases of reaction temperature,the cell parameters of BaTiO3 nanoparticles decrease,and the crystallite sizes increase.In addition,the formation mechanism of BaTiO3 nanoparticles prepared by molten salt method was also discussed.
出处 《功能材料》 EI CAS CSCD 北大核心 2010年第7期1165-1168,共4页 Journal of Functional Materials
基金 国家自然科学基金资助项目(50472080) 湖南省教育厅科学研究资助项目(06C829)
关键词 熔盐法 钛酸钡 BaO2·H2O2 纳米粒子 molten salt method barium titanate BaO2·H2O2 nanoparticle
  • 相关文献

参考文献12

二级参考文献182

共引文献73

同被引文献31

  • 1仲维卓,夏长泰,施尔畏,王步国,李文军,华素坤.水热条件下BaTiO3晶粒中OH^—缺陷的形成[J].人工晶体学报,1996,25(3):192-197. 被引量:10
  • 2马令娟,陈林深,陈诵英.制备工艺对NiFe_2O_4分解CO_2活性的影响[J].无机化学学报,2007,23(2):329-334. 被引量:2
  • 3Srinivasan G, Tatarenko A S, Mathe V, et al. Microwave and MM-wave magnetoelectric interactions in ferrite-ferroelectric bilayers[J]. Eur Phys J B, 2009, 71(3): 371-375.
  • 4Pileni M P. Magnetic Fluids: Fabrication, Magnetic Properties, and Organization of Nanocrystals[J]. Adv Funct Mater, 2001, 11(5): 323-336.
  • 5Shultz M D, Calvinb S, Fatourosc P P, et al. Enhanced ferrite nanoparticles as MRI contrast agents[J]. Journal of Magnetism and Magnetic Materials, 2007, 311(1): 464-468.
  • 6Wang S X, Zhou Y, Sun W T. Preparation and characterization of antifouling thermosensitive magnetic nanopaxticles for applications in biomedicine[J]. Materials Science and Engineering C, 2009,29(4): 1196-1200.
  • 7Parmar H, Desai R, Upadhyay R V. Structural characterization of microwave-synthesized zinc-substituted cobalt ferrite nanoparticles[J]. Appl Phys A, 2011, 104(1): 229-234.
  • 8Chang M T, Chou L J, Hsien C. H, et al. Magnetic and Electrical Characterizations of Half-Metallic Fe304 Nanowires[J]. Adv Mater, 2007, 19(17):2290-2295.
  • 9Sugimoto M. The Past, Present, and Future of Ferrites[J]. J Am Ceram Soc, 1999, 82(2): 269-280.
  • 10Siddique M, Butt N M. Effect of particle size on degree of inversion in ferrites investigated by Mossbauer spectroscopy[J]. Physica B, 2010, 405(19): 4211-4215.

引证文献2

二级引证文献2

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部