期刊文献+

Research on micro-structure and catalysis properties of nanosized Ce_(1–x)(Fe_(0.5)Eu_(0.5))_xO_(2–δ) solid solutions 被引量:5

Research on micro-structure and catalysis properties of nanosized Ce_(1–x)(Fe_(0.5)Eu_(0.5))_xO_(2–δ) solid solutions
原文传递
导出
摘要 Nanosized Fe^3+ and Eu^3+ codoped CeO2 solid solutions were synthesized via hydrothermal method. The crystalline structure of Ce1-x(Fe0.5Eu0.5)xO2-δx=0.00–0.30) solid solutions was carried out by the X-ray diffraction technique, and the spectrum features were identified by UV-Vis and Raman spectroscopy, respectively. It was observed that the cell parameters were first increased then decreased by increasing the doped ions content. The phase separation was detected when the dopant concentration reached to x=0.30. UV-Vis spectrum showed that the width of the band gap gradually reduced by increasing the doped content, and the solid solubility was determined to be x=0.20. The Raman technique displayed that the peak position of F2g mode gradually shifted to lower frequencies from 465 cm^–1 for x=0.00 to 440 cm^–1 for x=0.20. The catalytic effects of Ce1-x(Fe0.5Eu0.5)xO2-δsolid solutions on the electrochemistry properties of Mg2Ni/Ni were measured by mixing them together via ball milling technique. The electrochemical properties of the Mg_2Ni/Ni-Ce1-x(Fe0.5Eu0.5)xO2-δcomposites showed that the maximum discharge capability Cmax and the cycle stability were improved obviously. Meanwhile, the EIS characteristic also indicated that the doped solid solutions could enhance the rate of charge transfer on the surface of alloy. The catalytic effect of the solid solutions was speculated to rely on both the concentration of oxygen vacancies and the cell volumes of the solid solutions. Nanosized Fe^3+ and Eu^3+ codoped CeO2 solid solutions were synthesized via hydrothermal method. The crystalline structure of Ce1-x(Fe0.5Eu0.5)xO2-δx=0.00–0.30) solid solutions was carried out by the X-ray diffraction technique, and the spectrum features were identified by UV-Vis and Raman spectroscopy, respectively. It was observed that the cell parameters were first increased then decreased by increasing the doped ions content. The phase separation was detected when the dopant concentration reached to x=0.30. UV-Vis spectrum showed that the width of the band gap gradually reduced by increasing the doped content, and the solid solubility was determined to be x=0.20. The Raman technique displayed that the peak position of F2g mode gradually shifted to lower frequencies from 465 cm^–1 for x=0.00 to 440 cm^–1 for x=0.20. The catalytic effects of Ce1-x(Fe0.5Eu0.5)xO2-δsolid solutions on the electrochemistry properties of Mg2Ni/Ni were measured by mixing them together via ball milling technique. The electrochemical properties of the Mg_2Ni/Ni-Ce1-x(Fe0.5Eu0.5)xO2-δcomposites showed that the maximum discharge capability Cmax and the cycle stability were improved obviously. Meanwhile, the EIS characteristic also indicated that the doped solid solutions could enhance the rate of charge transfer on the surface of alloy. The catalytic effect of the solid solutions was speculated to rely on both the concentration of oxygen vacancies and the cell volumes of the solid solutions.
作者 张国芳 许剑轶 侯忠辉 王青春 ZHANG Guofang XU Jianyi HOU Zhonghui WANG Qingchun(School of Material and Metallurgy, Inner Mongolia University of Science and Technology, Baotou 014010, China Key Laboratory of lntergrate Explora- tion of Baiyun Obo Multi-metal Resources, Inner Mongolia University of Science and Technology, Baotou 014010, China)
出处 《Journal of Rare Earths》 SCIE EI CAS CSCD 2017年第1期63-70,共8页 稀土学报(英文版)
基金 Project supported by the National Natural Science Foundation of China(51501059) Talent Incubation Funding of School of Materials and Metallurgy and Inner Mongolia University of Science and Technology(2014CY012)
关键词 solid solution HYDROTHERMAL MG2NI catalysis effect electrochemistry property rare earths solid solution hydrothermal Mg2Ni catalysis effect electrochemistry property rare earths
  • 相关文献

参考文献4

二级参考文献49

  • 1赖为华,余成洲.提高MH-Ni电池放电电压平台的途径[J].电池,1996,26(4):189-191. 被引量:24
  • 2Huang, W.; Shuk, P.; Greenblatt, M. Solid State Ionics 1998, 113, 305.
  • 3Rajendran, M.; Mallick, K. K.; Bhttacarya, A. K. J. Mater. Sci. 1998, 33, 5001.
  • 4Riley, B. J. Power Sources 1990, 29, 223.
  • 5Shuk, P.; Greenblatt, M.; Crft, M. J. Alloys Compd. 2000, 303-304, 465.
  • 6Li, L. P.; Li, G. S.; Che, Y. L.; Su, W. H. Chem. Mater. 2000, 12, 2567.
  • 7McBride, J. R.; Hass, K. C.; Poindexter, B. D.; Weber, W. H. J. Appl. Phys. 1994, 78(4), 2435.
  • 8Edmond, A.; Rafeh, B.; Jean, G..; Antoine, A. Chem. Mater. 1993, 5, 193.
  • 9Wagner, C. D. Handbook of X-ray Photoelectron Spectroscopy, Ed.: Perkin Elmer Corporation Physical Electronics Division, Plenum Press, New York, 1979, pp. 89-121.
  • 10Li, G. S.; Mao, Y. C.; Li, L. P.; Feng, S. H. Chem. Mater. 1999, 11, 1259.

共引文献35

同被引文献7

引证文献5

二级引证文献5

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