Mechanism of phosphorescence appropriate for the long-lasting phosphors Eu2+-doped SrAl2O4 with codopants Dy3+ and B3+

被引:663
作者
Clabau, F
Rocquefelte, X
Jobic, S
Deniard, P
Whangbo, MH
Garcia, A
Le Mercier, T
机构
[1] Inst Mat Jean Rouxel, Chim Solide Lab, UMR 6502, F-44340 Nantes, France
[2] N Carolina State Univ, Dept Chem, Raleigh, NC 27695 USA
[3] CNRS, Inst Chim Matiere Condensee Bordeaux, F-33608 Pessac, France
[4] Ctr Rech Aubervilliers, F-93308 Aubervilliers, France
关键词
D O I
10.1021/cm050763r
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
The existing mechanisms proposed to explain the phosphorescence of SrAl2O4:Eu2+,Dy3+ and related phosphors were found to be inconsistent with a number of important experimental and theoretical observations. We formulated a new mechanism of phosphorescence on the basis of the facts that the d orbitals of Eu2+ are located near the conduction band bottom of SrAl2O4, that the Eu2+ concentration decreases during UV excitation, and that trace amounts of Eu3+ are always present in these phosphors. In our mechanism, some Eu2+ ions are oxidized to Eu3+ under UV, and the released electrons are trapped at the oxygen vacancy levels located in the vicinity of the photogenerated Eu3+ cations. The phosphorescence arises from the recombination of these trapped electrons around the photogenerated Eu3+ sites with emission at 520 nm. The codopant Dy3+ enhances the phosphorescence by increasing the number and the depth of electron traps, and the codopant B3+ enhances the phosphorescence by increasing the depth of electron traps. We also probed the origin of another emission at 450 nm of SrAl2O4:Eu2+ that occurs at low temperatures. Our analysis indicates that this emission is caused by a charge transfer from oxygen to Eu3+ cations and is associated with a hole trapping.
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页码:3904 / 3912
页数:9
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