4.6 Article

Reflux synthesis, formation mechanism, and photoluminescence performance of monodisperse Y2O3:Eu3+ nanospheres

期刊

MATERIALS CHEMISTRY AND PHYSICS
卷 117, 期 1, 页码 234-243

出版社

ELSEVIER SCIENCE SA
DOI: 10.1016/j.matchemphys.2009.05.047

关键词

Nanostructures; Oxides; Chemical synthesis; Luminescence

资金

  1. Natural Science Foundation of Shanghai [08ZR1407600]
  2. Shanghai Educational Development Foundation [2008CG49]
  3. Innovation Program of Shanghai Municipal Education Commission [09YZ18]
  4. Key Project of Chinese Ministry of Education [208182]
  5. Academic Leader Program of Shanghai Science and Technology Committee [07XD14014]
  6. Leading Academic Discipline Project of Shanghai Municipal Education Commission [J50102]
  7. National High Technology Research and Development Program (863 Program) of China [2007AA03Z335]
  8. Shanghai Special Foundation for Selected Cultivation of Excellent Young University Teacher

向作者/读者索取更多资源

Monodisperse Y2O3:Eu3+ nanospheres have been successfully synthesized by a low-temperature reflux method assisted by cetyltrimethyl ammonium bromide (CTAB). The products were characterized by Xray diffraction spectroscopy, transmission electron microscopy, scanning electron microscopy, Fourier-transform infrared spectrophotometer, thermogravimetric and differential thermal analysis, and X-ray photoelectron spectroscopy. It is demonstrated that the size of Y2O3:Eu3+ nanospheres can be controlled from 80 to 140 nm with narrow size distribution by adjusting the amount of CTAB. A possible formation mechanism of Y2O3:Eu3+ nanospheres has been proposed. The photoluminescence analysis shows that Y2O3:Eu3+ nanospheres obtained have a strong red emission peak of Eu3+ ions at around 611 nm, due to the D-5(0) -> F-7(2) forced electric dipole transition of Eu3+ ions. It is found that the photoluminescence performance of the obtained Y2O3:Eu3+ nanospheres is stronger than that of the Y2O3:Eu3+ nanorods synthesized by a traditional hydrothermal route. (c) 2009 Elsevier B.V. All rights reserved.

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