Laser spectroscopy of Pr3+ ions in LiKY1-xPrxF5 single crystals

被引:64
作者
Balda, R
Fernández, J
de Ocáriz, IS
Voda, M
García, AJ
Khaidukov, N
机构
[1] Russian Acad Sci, Kurnakov Inst Gen & Inorgan Chem, Moscow, Russia
[2] Univ Basque Country, Dept Fis Aplicada I, ETSII & Telecom, Bilbao 48013, Spain
关键词
D O I
10.1103/PhysRevB.59.9972
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
The visible luminescence of Pr3+-doped fluoride LiKY1-xPrxF5 crystals (x = 0.001, 0.01, 0.02, 0.03, 0.05, and 0.1) has been investigated as a function of concentration and temperature by using time-resolved laser spectroscopy. The temperature-dependent concentration quenching of the P-3(0) fluorescence in the 10-77 K temperature range can be described in the framework of a thermally activated cross-relaxation process involving the D-1(2) and H-3(6) states. However, the single exponential character of the decays at all concentrations and temperatures suggests that energy migration is also present in this system. The fluorescence from the D-1(2) level shows a strong concentration quenching for Pr3+ concentrations higher than x = 0.001 even at 4.2 K. The time evolution of the decays from the D-1(2) state for concentrations higher than x = 0.001 is consistent with a dipole-dipole energy transfer mechanism. Anti-Stokes emission from the P-3(0) level following excitation of the D-1(2) state is also studied for different Pr3+ concentrations. Analysis of the upconverted fluorescence decays supports that the mechanism responsible for the upconvertion process is energy transfer. However, this process seems to be complex enough to allow for the use of a single model which could explain the behavior observed. [S0163-1829(99)04615-9].
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页码:9972 / 9980
页数:9
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