The enhancement of luminescence in Co-doped cubic Eu2O3 using Li+ and Al3+ ions

被引:40
作者
Chae, Ki-Woong [2 ]
Park, Ta-Ryeong [3 ]
Cheon, Chae Il [1 ,2 ]
Cho, Nam In [4 ]
Kim, Jeong Seog [1 ,3 ]
机构
[1] Hoseo Univ, Dept Semicond & Display Engn BK21, Asan 336795, Chungnam, South Korea
[2] Hoseo Univ, Dept Mat Sci & Engn, Asan 336795, Chungnam, South Korea
[3] Hoseo Univ, Dept Display Engn, Asan 336795, Chungnam, South Korea
[4] Sunmoon Univ, Dept Elect Engn, Asan 336708, Chungnam, South Korea
关键词
Cubic Eu2O3; Co-doping; Enhancement; Luminescence; XPS; Raman; THIN-FILM PHOSPHORS; SURFACE; TRANSITION; VALENCE; STATE; RAMAN;
D O I
10.1016/j.jlumin.2011.06.017
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The co-doping of Li+ and Al3+ ions drastically enhances the luminescence of cubic Eu2O3. The integrated emission intensity of D-5(0)-> F-7(J) bands (J=1-4) at 580-710 nm increases by a factor of about 6.7 in the co-doped Eu2O3 compared to the un-doped Eu2O3. In order to confirm that the co-doped ions were actually incorporated into the host lattice, the structural characteristics were studied using Raman spectroscopy, XPS, XRD, photoluminescence lifetime, and an SEM. These analyses consistently indicate a certain structural evolution in their results with an increase in the co-doping concentration. Variations in the crystal structure, the crystal morphology, and the intensity variation of the Raman modes at 465 and 483 cm(-1) are presented as the evidences showing the incorporation of the co-doped ions into the host. The luminescence enhancement is discussed in terms of concentration quenching, reduction of defect sites, and the modification of the local symmetry of the Eu3+ ions, especially in the inversion symmetry sites. (C) 2011 Elsevier B.V. All rights reserved.
引用
收藏
页码:2597 / 2605
页数:9
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