Scintillation properties and increased vacancy formation in cerium and calcium co-doped yttrium aluminum garnet

被引:7
作者
Dickens, Peter T. [1 ]
Haven, Drew T. [1 ]
Friedrich, Stephan [2 ]
Lynn, Kelvin G. [1 ]
机构
[1] Washington State Univ, Ctr Mat Res, Pullman, WA 99164 USA
[2] Lawrence Livermore Natl Lab, 7000 East Ave,L 188, Livermore, CA 94550 USA
关键词
Czochralski method; Scintillator materials; Scintillators; Doping; Defects; Single crystal growth; X-RAY SPECTROMETER; DEFECT STRUCTURE; YAG CRYSTALS; CE; LSO; PERFORMANCE; RESOLUTION; STATE;
D O I
10.1016/j.jcrysgro.2018.10.059
中图分类号
O7 [晶体学];
学科分类号
0702 ; 070205 ; 0703 ; 080501 ;
摘要
Co-doping with divalent elements is known to improve the light yield and decay times of some cerium-activated scintillators, despite the stabilization of tetravalent Ce4+, previously believed to be non-luminescent, from the Ce3+ state. Ce4+ stabilization is a charge compensation mechanism which results from divalent ion substitution of a 3 + site. To elucidate the underlying mechanisms, which remain poorly understood, we have grown three Ce,Ca:YAG crystals with different amounts of calcium co-dopants by the Czochralski method and characterized their scintillation and defect properties. Calcium co-doping reduces the decay times and stabilizes the formation of Ce4+ as expected. Interestingly, X-ray fluorescence analysis reveals a decreased concentration of cerium within the YAG crystal for the sample doped with high levels of Ca, which could contribute to the observation that scintillator properties are improved only for low levels of Ca co-doping. Additionally, positron annihilation spectroscopy reveals an increase in the concentration of vacancies with increasing Ca concentration, while thermoluminescence is observed to show no detectable signal. Furthermore, room temperature photo-luminescence of the Ce 4f to 5d(1) transition demonstrates decreased emission with increasing Ca co-doping. These data suggest that Ca co-doping decreases the decay time by creating defects with non-radiative decay pathways.
引用
收藏
页码:16 / 22
页数:7
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