Abstract
CaTiO3:Pr3+ phosphor with a single red emission peak of around 613nm was co-doped with In3+ to charge compensate in the lattice sites where a trivalent ion Pr3+ substitutes a divalent Ca2+ ion. This phosphor was prepared via the solid state reaction process. The concentration of In3+ was varied from 0.05 to 0.3mol% and it was found that the In3+ incorporation enhanced the intensity of the red emission and the afterglow decay time of the CaTiO3:Pr3+ phosphor considerably. It is most likely that the incorporated In3+ charge compensators enhanced the luminescence intensity of the phosphor by neutralizing the additional positive charge generated by the Pr3+ ions when substituting in the Ca2+ ions site. The orthorhombic CaTiO3 phase was identified by X-ray diffraction. Scanning electron microscopy images showed agglomerated particles with different shapes and sizes. A single red emission of Pr3+ of around 613nm and phosphorescence decay time of 6min were measured using photoluminescence (PL) spectroscopy and afterglow measurements, respectively. Diffuse reflectance spectroscopy was used to determine the absorbing centres of the phosphor.
Original language | English |
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Pages (from-to) | 141-146 |
Number of pages | 6 |
Journal | Powder Technology |
Volume | 237 |
DOIs | |
Publication status | Published - Mar 2013 |
Externally published | Yes |
Keywords
- CaTiO:Pr
- Charge compensation
- Intervalence charge transfer
- Long afterglow phosphors
ASJC Scopus subject areas
- General Chemical Engineering