Article ID | Journal | Published Year | Pages | File Type |
---|---|---|---|---|
1873874 | Physics Procedia | 2009 | 9 Pages |
Photoluminescence and time resolved photoluminescence spectra of Y V O4 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 1D23→H4 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 Y V O4 host luminescence. The quenching of the 1D23→H4 emission with increasing pressure is accompanied by a shortening of its lifetime from 12.5 μs at ambient pressure to less than 3 μs 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).