High pressure luminescence of YVO4:Pr3+

被引:1
作者
Mahlik, S. [1 ]
Grinberg, M. [1 ]
Cavalli, E. [2 ]
Bettinelli, M. [3 ]
Boutinaud, P. [4 ]
机构
[1] Univ Gdansk, Inst Expt Phys, Wita Stwosza 57, PL-80952 Gdansk, Poland
[2] Univ Parma, Dipartimento Chim Gen & Inorgan, Dipartimento Chim Analit, Dipartimento Chim Fis, Parma, Italy
[3] Univ Verona, INSTM, Dipartimento Sci Tecnolog, Verona, Italy
[4] Univ Blaise Pascal, Lab Mat Inorgan, Aubiere, France
来源
2008 INTERNATIONAL CONFERENCE ON LUMINESCENCE AND OPTICAL SPECTROSCOPY OF CONDENSED MATTER | 2009年 / 2卷 / 02期
关键词
trapped exciton; YVO4:Pr3+; YVO4; CRYSTALS; PR3+; PHOSPHORS; DYNAMICS; LINBO3;
D O I
10.1016/j.phpro.2009.07.044
中图分类号
O469 [凝聚态物理学];
学科分类号
070205 ;
摘要
Photoluminescence and time resolved photoluminescence spectra of YVO4 doped with Pr3+ obtained at high hydrostatic pressure up to 76 kbar applied in a diamond anvil cell are presented. At pressures lower than 60 kbar the steady state emission spectra consist of sharp lines peaking between 600 and 625 nm, related to (D2 -> H4)-D-1-H-3 transition in Pr3+ and two lines at 475 nm and 575 nm related to an uncontrolled amount of Dy3+ ions. At pressures above 68 kbar the Pr3+ and Dy3+ emission intensity decreases and the corresponding bands are replaced by a broad band peaking at 530 nm attributed to perturbed YVO4 host luminescence. The quenching of the (D2 -> H4)-D-1-H-3 emission with increasing pressure is accompanied by a shortening of its lifetime from 12.5 mu s at ambient pressure to less than 3 mu s at 60 kbar and has been attributed to nonradiative transition to the charge transfer exciton trapped at Pr3+ ion (Pr4++ electron bound by the Coulomb potential).
引用
收藏
页码:577 / 585
页数:9
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