Optical spectroscopy of Ca3Sc2Si3O12, Ca3Y2Si3O12 and Ca3Lu2Si3O12 doped with Pr |
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Authors: | K.V. Ivanovskikh A. Meijerink A. Speghini C. Ronda M. Bettinelli |
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Affiliation: | a CMI, Debye Institute for Nanomaterials Science, Utrecht University, P.O. Box 80 000, 3508TA Utrecht, The Netherlands b Laboratory of Solid State Chemistry, DB, University of Verona, and INSTM, UdR Verona, Strada Le Grazie 15, 37134 Verona, Italy c DiSTeMeV, University of Verona, and INSTM, UdR Verona, Via della Pieve 70, 37029 San Floriano (VR), Italy d Budker Institute of Nuclear Physics SB RAS, Lavrentiev prospect 11, 630090 Novosibirsk, Russian Federation e Philips Research Europe-Aachen, Weisshausstrasse 2, D-52066 Aachen, Germany f Zhejiang University, Centre for Optical and Electromagnetic Research, Hangzhou 310058, China |
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Abstract: | 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. |
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Keywords: | 5d-4f luminescence of Pr3+ Energy transfer Time-resolved spectroscopy |
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