Annihilation of the persistent luminescence of MAl2O4 :Eu2+ by Sm3+ co-doping

被引:28
作者
Altasalo, T
Deren, P
Hölsä, J
Jungner, H
Lastusaari, A
Niittykoski, J
Strek, W
机构
[1] Univ Turku, Dept Chem, Inorgan Chem Lab, FIN-20014 Turku, Finland
[2] Grad Sch Mat Res, Turku, Finland
[3] Polish Acad Sci, Inst Low Temp & Struct Res, PL-50950 Wroclaw, Poland
[4] Univ Helsinki, Dating Lab, FIN-00014 Helsinki, Finland
关键词
persistent luminescence; calcium aluminate; europium; samarium co-doping;
D O I
10.1016/j.radmeas.2004.01.009
中图分类号
TL [原子能技术]; O571 [原子核物理学];
学科分类号
0827 ; 082701 ;
摘要
The calcium aluminates doped with the Eu2+ and Nd3+ ions, CaAl2O4:Eu2+,Nd3+, are a novel and efficient persistent luminescence (i.e. afterglow) material. The Nd3+ ions were found to enhance the persistent luminescence. Some other R3+ co-dopants had similar or opposite, though weaker, effect. The Sm3+ (and Yb3+) ions suppressed almost completely the persistent luminescence and thermoluminescence of the Eu2+ ion. From the UV-excited luminescence and persistent luminescence spectra it was found that the Eu2+ ion acts as a luminescent centre with luminescence at the blue ( lambda(max) = 440 nm) region. The Sm3+ ion was reduced to the divalent state. The thermoluminescence glow curves of the CaAl2O4:Eu2+,Sm3+ material showed that the high-temperature glow peaks, i.e. deep traps, were suppressed almost completely. The Nd:YAG laser-excited high-resolution photoluminescence of the Sm2+ ion confirmed that the Eu2+ ion occupies only one Ca2+ site. Only weak perturbations were observed in the Sm2+ site due to the changes in the environment of the Sm2+ site. (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:515 / 518
页数:4
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