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Preparation of Compensation Ions Codoped SrTiO3:Pr3+ Red Phosphor with the Sol-Gel Method and Study of Its Luminescence Enhancement Mechanism
SrTiO3:Pr3+ is the most representative titanate matrix red phosphor for field emission display (FED). The red luminous efficiency of SrTiO3:Pr3+ will be greatly improved after the compensation ions codoping, so SrTiO3:Pr3+ red phosphor has been a research focus at home and abroad. SrTiO3:Pr3+, SrTiO...
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Published in: | Advances in OptoElectronics (Hindawi) 2014-01, Vol.2014 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Online Access: | Get full text |
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Summary: | SrTiO3:Pr3+ is the most representative titanate matrix red phosphor for field emission display (FED). The red luminous efficiency of SrTiO3:Pr3+ will be greatly improved after the compensation ions codoping, so SrTiO3:Pr3+ red phosphor has been a research focus at home and abroad. SrTiO3:Pr3+, SrTiO3:Pr3+, Mg2+, and SrTiO3:Pr3+, Al3+ phosphors are synthesized by a new sol-gel method. Crystal structure, spectral characteristics, and luminescence enhancement mechanism of the sample were studied by XRD and PL spectra. The results showed that after co-doped, SrTiO3:Pr3+ phosphor is single SrTiO3 cubic phase, the main emission front is located at 614 nm, corresponding to Pr3+ ions 1D2→3H4 transition emission. SrTiO3:Pr3+, Mg2+ and SrTiO3:Pr3+, Al3+ phosphor luminescence intensity is enhanced, but the main luminescence mechanism is not changed. Acceptor impurity x = Mg2+, Al3+ will replace Ti bit after being doped into the crystal lattice to form XTi- charge compensation corresponding defect centers PrSr+ to reduce the demand of Sr2+ or Ti3+ vacancy. While Sr-doped Pr will make lattice distortion and transition energy of 4f-5d is very sensitive to crystal electric field changes around Pr atom. Doping different impurities will make electric field distribution around the icon have a different change. It increases energy transfer of 4f-5d transition and improves the luminous intensity of SrTiO3:Pr3+ red phosphor. |
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ISSN: | 1687-563X 1687-5648 |
DOI: | 10.1155/2014/674780 |