Delocalization, thermal ionization, and energy transfer in singly doped and codoped CaAl4O7 and Y2O3 -: art. no. 235113

被引:19
作者
Jia, DD [1 ]
Wang, XJ
Yen, WM
机构
[1] Univ Puerto Rico, Dept Phys, Mayaguez, PR 00681 USA
[2] Chinese Acad Sci, Changchun Inst Opt Fine Mech & Phys, Key Lab Excited State Proc, Changchun 130033, Peoples R China
[3] Georgia So Univ, Dept Phys, Statesboro, GA 30460 USA
[4] Univ Georgia, Dept Phys & Astron, Athens, GA 30602 USA
基金
美国国家科学基金会;
关键词
D O I
10.1103/PhysRevB.69.235113
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Ce3+ and Tb3+ singly doped and codoped CaAl4O7 and Y2O3 single crystal fibers were grown using the laser heated pedestal growth method. Energy transfer from Ce3+ to Tb3+ was studied in these samples. No energy transfer between Ce3+ and Tb3+ was observed in codoped Y2O3. This is because electrons excited into the Ce3+ 5d states delocalize into the conduction band at a rate that is faster than the interionic energy transfer rate, whereas the converse is the case for CaAl4O7 doped with Ce3+ (1 at %) and Tb3+ (1 at %). The energy transfer rate was determined to be on the order of 10(9) s(-1). The transfer occurs before the excited electrons can be thermally promoted into the conduction band. From these results, it can be inferred that the thermal ionization rate (W-Th) from the lowest 5d excited Ce3+ state at 355 nm is less than 10(9) s(-1) at room temperature, whereas the delocalization rate (W-D) into the conduction band is faster than this rate. The location of the Tb3+ and Ce3+ states relative to the valence and conduction band of these two materials has been determined through photoconductivity measurements.
引用
收藏
页码:235113 / 1
页数:5
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