Luminescent and structural properties of manganese-doped zinc aluminate spinel nanocrystals

被引:53
|
作者
Tsai, Mu-Tsun [1 ]
Chang, Yee-Shin [2 ]
Huang, Ing-Bang [1 ]
Pan, Bo-Yu [1 ]
机构
[1] Natl Formosa Univ, Dept Mat Sci & Engn, Huwei 632, Yunlin, Taiwan
[2] Natl Formosa Univ, Dept Elect Engn, Huwei 632, Yunlin, Taiwan
关键词
Powders; Sol-gel processes; ZnAl2O4:Mn; Photoluminescence; ZNAL2O4; PHOTOLUMINESCENCE; PHOSPHORS; GREEN;
D O I
10.1016/j.ceramint.2012.10.201
中图分类号
TQ174 [陶瓷工业]; TB3 [工程材料学];
学科分类号
0805 ; 080502 ;
摘要
Manganese-doped zinc aluminate spinel (ZnAl2O4:Mn; Mn=0-6.0 mol%) phosphor nanoparticles were prepared by the sol gel process. The effects of thermal annealing and dopant concentration on the structure, microstructure and luminescence of the powder phosphors were investigated. The X-ray diffraction (XRD) and Fourier transform infrared (FT-IR) results confirmed that a single-phase spinel started to crystallize at around 600 degrees C for the investigated powders. On heating at 600-1200 degrees C, the powders had the average crystallite sizes of around 12-33 nm. The crystallite size and lattice constant increased as the doping level of Mn increased. FT-IR spectra exhibited only absorption bands of the AlO6 octahedral groups, which suggested that the powder phosphors mainly crystallized in a normal spinel structure. Scanning electron microscopy (SEM) investigations showed the primary particle sizes were around 20-25 nm for the powders annealed at 1000 degrees C, and less than ca. 50 nm for those annealed at 1200 degrees C. Photoluminescence (PL) spectra under UV or visible light 6 excitation exhibited a strong green emission band centered at 510 nm, corresponding to the typical T-4(1)((4)G)-(6)A(1)(S-6) transition of tetrahedral Mn2+ ions. The most intense PL emission was obtained by exciting at 458 nm. The PL intensity was significantly enhanced by the improved crystallinity and diminished OH- groups. Optimum brightness occurred at a doping of 3.0 mol% Mn. (C) 2012 Elsevier Ltd and Techna Group S.r.l. All rights reserved.
引用
收藏
页码:3691 / 3697
页数:7
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