Optical transition and luminescence properties of Sm3+‐doped YNbO4 powder phosphors
A series of YNbO4: Sm3+ powder phosphors with different doping concentrations were synthesized by a traditional high‐temperature solid‐state reaction method. The crystal structure of the obtained samples was characterized by means of X‐ray diffraction. Concentration quenching, energy‐transfer mechan...
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Veröffentlicht in: | Journal of the American Ceramic Society 2020-02, Vol.103 (2), p.1037-1045 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | A series of YNbO4: Sm3+ powder phosphors with different doping concentrations were synthesized by a traditional high‐temperature solid‐state reaction method. The crystal structure of the obtained samples was characterized by means of X‐ray diffraction. Concentration quenching, energy‐transfer mechanism, and luminescence thermal stability of YNbO4: Sm3+ samples were studied through the fluorescence spectra and decays. It was concluded that electric dipole‐dipole interaction was the dominant energy‐transfer mechanism between Sm3+ ions according to both Van Uitert's model and Dexter's model. Using the Arrhenius model, crossover process was proven to be responsible for the luminescence thermal quenching of Sm3+. Moreover, a novel approach for evaluating the optical transition properties of Sm3+ ion in YNbO4 powders using the diffuse‐diffraction spectrum and fluorescence decay was examined in the framework of Judd‐Ofelt (J‐O) theory. It was confirmed that the J‐O parameters Ωλ (λ = 2, 4, 6) of Sm3+ in YNbO4 powder were reliable by comparing the radiation transition rate with the measured emission results.
A novel approach for evaluating the optical transition properties of Sm3+ ion in YNbO4 powders using the diffuse‐diffraction spectrum and fluorescence decay was examined in the framework of Judd‐Ofelt (J‐O) theory. The obtained J‐O parameters Ωλ (λ = 2, 4, 6) were reliable by comparing the radiation transition rate with the measured emission results. |
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ISSN: | 0002-7820 1551-2916 |
DOI: | 10.1111/jace.16717 |