Optical spectroscopy of Ca3Sc2Si3O12, Ca3Y2Si3O12 and Ca3Lu2Si3O12 doped with Pr3+

被引:73
作者
Ivanovskikh, K. V. [1 ]
Meijerink, A. [1 ]
Piccinelli, F. [2 ,3 ]
Speghini, A. [4 ,5 ]
Zinin, E. I. [6 ]
Ronda, C. [1 ,7 ,8 ]
Bettinelli, M. [2 ,3 ]
机构
[1] Univ Utrecht, Debye Inst Nanomat Sci, CMI, NL-3508 TA Utrecht, Netherlands
[2] Univ Verona, Lab Solid State Chem, DB, I-37134 Verona, Italy
[3] UdR Verona, INSTM, I-37134 Verona, Italy
[4] Univ Verona, DiSTeMeV, I-37029 San Floriano, VR, Italy
[5] UdR Verona, INSTM, I-37029 San Floriano, VR, Italy
[6] RAS, Budker Inst Nucl Phys, SB, Novosibirsk 630090, Russia
[7] Philips Res Europe Aachen, D-52066 Aachen, Germany
[8] Zhejiang Univ, Ctr Opt & Electromagnet Res, Hangzhou 310058, Zhejiang, Peoples R China
关键词
5d-4f luminescence of Pr3+; Energy transfer; Time-resolved spectroscopy; LUMINESCENCE; PHOTOLUMINESCENCE; PHOSPHOR; CE3+;
D O I
10.1016/j.jlumin.2009.12.031
中图分类号
O43 [光学];
学科分类号
070207 ; 0803 ;
摘要
The silicates Ca3Sc2Si3O12, Ca3Y2Si3O12 and Ca3Lu2Si3O12, both undoped and doped with Pr3+ ions, have been synthesized by solid-state reaction at high temperature. The luminescence spectroscopy and the excited state dynamics of the materials have been studied upon VUV and X-ray excitation using synchrotron radiation. All doped samples have shown efficient 5d-4f emission upon direct VUV excitation of 5d levels, but only Ca3Sc2Si3O12:Pr3+ shows luminescence upon interband VUV or X-ray excitation. The VUV excited emission spectra of Ca3Y2Si3O12:Pr3+ and Ca3Lu2Si3O12:Pr3+ show features attributed to emission from two distinct sites accommodating the Pr3+ dopant. The decay kinetics of the Pr3+ 5d-4f emission in Ca3Sc2Si3O12:Pr3+ upon VUV excitation across the band gap are characterized by decay times in the range 25-28 ns with no significant rise after the excitation pulse. They appear to be faster upon X-ray irradiation than for VUV excitation. Weak afterglow components are attributed to defect luminescence. (c) 2009 Elsevier B.V. All rights reserved.
引用
收藏
页码:893 / 901
页数:9
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