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Luminescent-center tuning for Ba6Ca3YAlSi6O24:Ce3+, Na+ orthosilicate phosphors
Ce3+ ion-doped Ba6Ca3YAlSi6O24 phosphors with a charge-compensating Na+ ion were prepared using a solid-state reaction. Ba6Ca3YAlSi6O24 was structurally characterized using synchrotron X-ray powder diffraction. The emission wavelengths of Ce3+ in different Ba2+ and Ca2+ sites with the distortion ind...
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Published in: | Journal of alloys and compounds 2019-03, Vol.777, p.572-577 |
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Main Authors: | , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Ce3+ ion-doped Ba6Ca3YAlSi6O24 phosphors with a charge-compensating Na+ ion were prepared using a solid-state reaction. Ba6Ca3YAlSi6O24 was structurally characterized using synchrotron X-ray powder diffraction. The emission wavelengths of Ce3+ in different Ba2+ and Ca2+ sites with the distortion index of polyhedrons in the host lattice were calculated. The photoluminescence excitation and emission spectra of the Ce3+-activated phosphors were site-selectively monitored; furthermore, the emission quenching as a function of Ce3+ content in the Ba6-2xCexNaxCa3YAlSi6O24 and Ba6Ca3-2xCexNaxYAlSi6O24 (x = 0.01–0.4) was clearly distinguished at relatively high concentrations of the activator. The Gaussian components of the phosphors were exploited by using the Ce3+ ion sites in the host lattice; in addition, the one and two luminescent centers for the Ba6-2xCexNaxCa3YAlSi6O24 and Ba6Ca3-2xCexNaxYAlSi6O24 phosphors, respectively, were identified. The sites of the luminescent centers for the calculated Ba6Ca3-2xCexNaxYAlSi6O24 composition was selectively tuned as the (BaCa)9-2xCexNaxYAlSi6O24 lattice structure.
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•Ba6Ca3YAlSi6O24:Ce3+, Na+ phosphors were prepared.•New phase of the Ba6Ca3YAlSi6O24 host was characterized.•Single and double luminescent centers were identified.•Ba6Ca3-2xCexNaxYAlSi6O24 was tuned as (BaCa)9-2xCexNaxYAlSi6O24. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2018.10.266 |