The enhancement of luminescence in Co-doped cubic Eu2O3 using Li+ and Al3+ ions
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Chae, Ki-Woong
[2
]
Park, Ta-Ryeong
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Hoseo Univ, Dept Display Engn, Asan 336795, Chungnam, South KoreaHoseo Univ, Dept Semicond & Display Engn BK21, Asan 336795, Chungnam, South Korea
Park, Ta-Ryeong
[3
]
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Cheon, Chae Il
[1
,2
]
Cho, Nam In
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Sunmoon Univ, Dept Elect Engn, Asan 336708, Chungnam, South KoreaHoseo Univ, Dept Semicond & Display Engn BK21, Asan 336795, Chungnam, South Korea
Cho, Nam In
[4
]
Kim, Jeong Seog
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Hoseo Univ, Dept Semicond & Display Engn BK21, Asan 336795, Chungnam, South Korea
Hoseo Univ, Dept Display Engn, Asan 336795, Chungnam, South KoreaHoseo Univ, Dept Semicond & Display Engn BK21, Asan 336795, Chungnam, South Korea
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
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.