Radiative energy transfer in ZnAl2O4:0.1% Ce3+, x% Eu3+ nanophosphor synthesized by sol-gel process

被引:19
作者
Motloung, S. V. [1 ]
Dejene, F. B. [1 ]
Kroon, R. E. [2 ]
Swart, H. C. [2 ]
Ntwaeaborwa, O. M. [2 ]
机构
[1] Univ Free State, Dept Phys, ZA-9866 Phuthaditjhaba, South Africa
[2] Univ Orange Free State, Dept Phys, ZA-9300 Bloemfontein, South Africa
基金
新加坡国家研究基金会;
关键词
Zinc aluminate; Cerium activated; Europium co-activated; Energy transfer; CIE; OPTICAL-PROPERTIES; LUMINESCENCE PROPERTIES; ZINC ALUMINATE; GLASS-CERAMICS; ZNAL2O4; PHOTOLUMINESCENCE; PHOSPHORS; NANOCRYSTALS; SPINEL; ZNS;
D O I
10.1016/j.physb.2015.04.007
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Zinc aluminate (ZnAl2O4) hosts and 0.1% Ce3+, x% Eu3+ co-activated ZnAl2O4 phosphor were successfully prepared at a relatively low temperature (similar to 80 degrees C) using the sol-gel method. The co-activator (Eu3+) concentration was varied in the range of 0 <= x <= 2 mol%, while the 0.1% Ce3+ was kept constant. The X-ray diffraction (XRD) data revealed that all annealed samples consisted of the pure cubic ZnAl2O4 structure. The estimated crystallite size was in the range of 18-21 nm in diameter. The results showed that the full width at half maximum (FWHM) increased with the increase in Eu3+ mol%, which suggested a decrease in particle size. The nanopowder microstructure revealed that the material consisted of non-uniform sizes and the loss of lattice fringes as the Eu3+ concentration was increased suggested the increase in strain or disorder. The photoluminescence (PL) results showed that the host, activated and co-activated nanophosphor emitted at different wavelengths. The peak shifts suggested that the luminescence might originate either from the defects in the host, Ce3+ or Eu3+ ions. The incorporation of the co-activator (Eu3+) at higher concentration resulted in radiative energy transfer from Ce3+ -> Eu3+. The CIE colour coordinates showed a shift from the blue to orange region as the Eu3+ concentration was increased. (C) 2015 Elsevier B.V. All rights reserved.
引用
收藏
页码:11 / 20
页数:10
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