Investigation on the optical sensing behaviors in single Eu3+-activated Sr2InSbO6 phosphors under green light excitation
•Luminescent behaviors of Sr2InSbO6:Eu3+ phosphors were presented under green light excitation.•The crystal structure and concentration quenching were investigated in detail.•The emission intensity remained 91.61% at 425 K.•The sensing sensitivity was analyzed based on the temperature-dependent deca...
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Veröffentlicht in: | Journal of alloys and compounds 2022-06, Vol.906, p.164322, Article 164322 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | •Luminescent behaviors of Sr2InSbO6:Eu3+ phosphors were presented under green light excitation.•The crystal structure and concentration quenching were investigated in detail.•The emission intensity remained 91.61% at 425 K.•The sensing sensitivity was analyzed based on the temperature-dependent decay curves.•The sensing sensitivity could be affected by the doping concentration of Eu3+ ions.
The sensing sensitivities of the Sr2InSbO6:Eu3+ phosphors with different doping concentrations were investigated based on the temperature-dependent decay curves. The crystal and electronic structure were studied by the X-ray diffractometer (XRD), Rietveld refinement, and X-ray photoelectron spectroscopy (XPS). In addition, the luminescent behaviors (e.g., photoluminescence spectra, concentration quenching, thermal stability, and luminescent dynamic) were investigated under the green light excitation (λex = 529 nm). The dominated peak was assigned to the 5D0 → 7F1 transition emitting an orange-red emission. Moreover, the obtained sample exhibited excellent thermal stability that the emission intensity remained 91.61% at 425 K. Eventually, the relative sensing sensitivity of the Sr2EuSbO6 phosphor was 0.766% K−1 and the doping concentration of Eu3+ ions greatly affected the sensing sensitivity. This work is the first time to investigate the single Eu3+-activated luminescent materials under the green light excitation. |
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ISSN: | 0925-8388 1873-4669 |
DOI: | 10.1016/j.jallcom.2022.164322 |