Combustion synthesis of nanostructured Ba0.8(Ca,Sr)0.2TiO3 ceramics and their dielectric properties

被引:4
作者
Singh, Laxman [1 ]
Kim, Ill Won [2 ]
Sin, Byung Cheol [1 ]
Rai, Uma Shanker [3 ]
Hyun, Seung Ho [4 ]
Lee, Youngil [1 ]
机构
[1] Univ Ulsan, Dept Chem, Ulsan 680749, South Korea
[2] Univ Ulsan, Dept Phys, Ulsan 680749, South Korea
[3] Banaras Hindu Univ, Dept Chem, Ctr Adv Study, Fac Sci, Varanasi 221005, UP, India
[4] Univ Ulsan, Sch Elect Engn, Ulsan 680749, South Korea
基金
新加坡国家研究基金会;
关键词
Dielectric properties; Perovskite; Combustion synthesis; Nanostructured; SOL-GEL; BARIUM-TITANATE; ELECTRICAL-PROPERTIES; IMPEDANCE ANALYSIS; BATIO3; POWDERS; THIN-FILMS; TEMPERATURE; CACU3TI4O12; GROWTH; NANOPARTICLES;
D O I
10.1016/j.ceramint.2015.06.044
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Ba-0.8(Ca,Sr)(0.2)TiO3 nanostructured ceramics were synthesized by a facile and glycine-assisted auto-combustion method using stable solid TiO2, which is better than other several chemical routes reported earlier involving expensive alkoxides, oxynitrates, or chlorides of titanium as the titanium sources. TGA/DSC analysis of precursor powder gives pre-information about formation of final product around 950 degrees C. XRD analysis confirms the formation of single-phase of the BCT and BST ceramics on sintering at 950 degrees C for 15 h. TEM image of the ceramics show nanocrystalline particles in the range 40-90 nm. Surface morphology indicates that the average grain size is in range of 55-140 nm and 45-120 nm for BCT and BST, respectively. Energy dispersive X-ray spectroscopy and X-ray photoelectron spectroscopy confirmed the purity and stoichiometry. The value of the dielectric constant of BST (epsilon(r) similar to 368) ceramic is higher than BCT (epsilon(r) similar to 255) at 100 Hz at 308 K. The dielectric constant BST is higher than BCT at all measured temperatures and frequency ranges due to higher crystallinity and high grain-boundary resistance, as confirmed by impedance analysis. (C) 2015 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:12218 / 12228
页数:11
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