Published June 2005 | Version v1
Journal article

Hydrothermal synthesis and luminescent properties of BaBeF4: RE (RE=Eu, Tb)

  • 1. Life Science and Chemistry School, Zhanjiang Normal College, Zhanjiang 524048 (China) and College of Sciences, South China Agricultural University, Wushan Road, Tianhe District, Guangzhou 510642 (China)
  • 2. Life Science and Chemistry School, Zhanjiang Normal College, Zhanjiang 524048 (China)
  • 3. Key Laboratory of Rare Earth Chemistry and Physics, Changchun Institute of Applied Chemistry, Chinese Academy of Sciences, Changchun 130022 (China)
  • 4. Faculty of Chemistry, Northeast Normal University, Changchun 130024 (China)

Description

The BaBeF4 powder has been hydrothermally synthesized from the double system. The effects of factors such as the ratio of initial reaction, pH value, reaction temperature and time were investigated. Moreover, the BaBeF4: RE (RE=Eu, Tb) phosphors were prepared by the hydrothermal method. Further, they were characterized by means of X-ray powder diffraction, scanning electron microscopy, thermogravimetric analysis, infrared spectroscopy and X-ray photoelectron spectroscopy. The luminescent properties were investigated by the luminescence spectrometer. The results show that the molar ratio and pH in the initial reaction mixture associated with the reaction temperature dominate the crystallization of the products. The products are air stable. XPS confirms the oxygen content of those products is very low. BaBeF4: RE obtained was pure phase of BaBeF4. It indicates that doping a low concentration of RE3+ ions could not change the structure. In the co-doped Eu3+ and Tb3+ system, Eu3+, Tb3+ and Eu2+ are observed in one matrix. These phenomena can be explained using an electron transfer theory. These RE ions occupy the sites of Ba2+ in BaBeF4. aBeF4

Additional details

Identifiers

DOI
10.1016/j.jssc.2005.03.032;
PII
S0022-4596(05)00123-4;

Publishing Information

Journal Title
Journal of Solid State Chemistry
Journal Volume
178
Journal Issue
6
Journal Page Range
p. 2167-2174
ISSN
0022-4596
CODEN
JSSCBI

Optional Information

Copyright
Copyright (c) 2005 Elsevier Science B.V., Amsterdam, The Netherlands, All rights reserved.