Synthesis of single-phase cubic Ce0.5Zr0.5O2 solid solution under high pressure and high temperature

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	Synthesis of single-phase cubic Ce0.5Zr0.5O2 solid solution under high pressure and high temperature
	D. P. Xu; Q. Y. Wang; G. M. Zhang; L. P. Li; W. H. Su
	2001
发表期刊	Chemical Journal of Chinese Universities-Chinese
ISSN	0251-0790
卷号	22 期号:4 页码:524-530
摘要	Using nanoparticles of CeO2 and ZrO2 prepared by chemical precipition method as the starting materials, the single-phase cubic Ce0.5Zr0.5O2 solid solution has been synthesized under high pressure and high temperature for the first time. The structural characteristics and valence state of the single-phase cubic Ce0.5Zr0.5O2 solid solution were investigated by XRD, TG-DTA, Raman, XPS and EPR measurements. The XRD results showed that the nanocrystalline mixtures of CeO2-50% ZrO2 can form a cubic Ce1-xZrxO2 solid solution above 1.67 GPa and above 1 073 Kt but the product is in a mixture state. The single-phase cubic Ce0.5Zr0.5O2 solid solution can be obtained only under the certain conditions of 3.1 GPa at 1 073 K. The high pressure promotes the process of the solid state reaction and the temperature of forming CeO2-ZrO2 solid solution decreases under high pressure. The DTA curve of the single-phase cubic Ce-0.5 Zr0.5O2 solid solution showed a broad exothermic peak between 403 K and 742 K. But the XRD pattern and Raman spectra displayed that the structure of the solid solution had not been changed before and after annealing at 773 K for 1 h. It revealed that the cubic Ce0.5Zr0.5O2 solid solution was stable in structure below 773 K. The EPR spectra recorded at room temperature gave an evidence of the presence of Ce3+ and O2- in CeO2 nanoparticles. However, the signals of Ce3+ and O2- have not been detected in Ce0.5Zr0.5O2 solid solution. An unknown signal (g = 1.990) has been observed in cubic Ce0.5Zr0.5O2 solid solution which has not been changed after annealing at 773 K for 1 h, exhibiting that there exists no Ce3+ in cubic Ce0.5Zr0.5O2 solid solution and the Ce4+ has not been reduced into Ce3+ after annealing. The hyperfine structure in Zr-3d XPS spectrum has been observed for the Ce0.5Zr0.5O2 solid solution. It shows that there may exist some Zr ions with a low valence-state. The ionic conductivity measured by impedance spectroscopy showed that the cubic Ce0.5Zr0.5O2 solid solution exhibits only the bulk conductivity. The bulk conductivity (sigma = 1.2 X 10(-5) S/cm at 823 K, sigma = 2.1 X 10(-3) S/cm at 1 123 K) is the same as that of CeO2, but smaller than that of Y2O3-stabilized ZrO2. A marked curvature at T = 823 K has been observed in the Arrhenius plot of the bulk conductivity. The activation energy below 823 K is lower than that above 823 K, and the reason has been discussed.
部门归属	jilin univ, dept phys, changchun 130023, peoples r china. jilin univ, key lab inorgan synth & preparat chem, changchun 130023, peoples r china. acad sinica, int ctr mat phys, shenyang 110015, peoples r china. ccast, world lab, ctr condensed matter & radiat phys, beijing 100080, peoples r china.;xu, dp (reprint author), jilin univ, dept phys, changchun 130023, peoples r china, peoples r china
关键词	Cerium Oxide Zirconium Oxide Nanocrystalline High-pressure And High-temperature Solid Solution Hydrothermal Synthesis Electrical-properties Zro2-ceo2 System Zirconia
URL	查看原文
WOS记录号	WOS:000168362300003
引用统计	被引频次：5[WOS] [WOS记录] [WOS相关记录]
文献类型	期刊论文
条目标识符	http://ir.imr.ac.cn/handle/321006/36854
专题	中国科学院金属研究所
推荐引用方式 GB/T 7714	D. P. Xu,Q. Y. Wang,G. M. Zhang,et al. Synthesis of single-phase cubic Ce0.5Zr0.5O2 solid solution under high pressure and high temperature[J]. Chemical Journal of Chinese Universities-Chinese,2001,22(4):524-530.
APA	D. P. Xu,Q. Y. Wang,G. M. Zhang,L. P. Li,&W. H. Su.(2001).Synthesis of single-phase cubic Ce0.5Zr0.5O2 solid solution under high pressure and high temperature.Chemical Journal of Chinese Universities-Chinese,22(4),524-530.
MLA	D. P. Xu,et al."Synthesis of single-phase cubic Ce0.5Zr0.5O2 solid solution under high pressure and high temperature".Chemical Journal of Chinese Universities-Chinese 22.4(2001):524-530.