4.7 Article

Tunable emission, energy transfer and thermal stability of Ce3+ , Tb3+ co-doped Na2BaCa(PO4)2 phosphors

Journal

JOURNAL OF RARE EARTHS
Volume 40, Issue 6, Pages 878-887

Publisher

ELSEVIER
DOI: 10.1016/j.jre.2021.05.016

Keywords

Na2BaCa(PO4)(2); Luminescence properties; Energy transfer; Tunable emission; Thermal stability; Rare earths

Funding

  1. National Natural Science Foundation of China [51772330, 51472273]
  2. Natural Science Foundation of Hunan Province [2017JJ2403]
  3. Key Research Foundation of Education Bureau of Hunan Province [16A220]

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This study synthesized a series of Ce3+ doped and Ce3+ and Tb3+ co-doped Na2BaCa(PO4)2 (NBCP) phosphors by conventional solid-stated reaction method. The color-tunable emission from blue to green was achieved by adjusting the Tb3+ concentration. The energy transfer efficiency from Ce3+ to Tb3+ ions was found to be as high as 91.5%. The optimal phosphor exhibited excellent thermal stability and has potential applications in general lighting and display fields.
A series of single Ce3+ doped and Ce3+ and Tb3+ co-doped Na2BaCa(PO4)(2) (NBCP) phosphors was synthesized by conventional solid-stated reaction method. The crystal structure, luminescence properties, thermal stability and energy transfer were carefully investigated. Ce3+ is inferred to substitute the Ba2+ site in NBCP lattice. The color-tunable emission from blue to green is observed by adjusting Tb3+ concentration among NBCP:0.03Ce(3+),yTb(3+) phosphors. The energy transfer behavior from Ce3+ to Tb3+ ions is both illustrated by co-doped PL spectra and decay curves. The energy transfer efficiency is as high as 91.5%. The mechanism of energy transfer is resonance type of dipole-dipole transition. In this work, the optimal phosphor exhibits the excellent thermal stability which keeps at 94.9% of that initial value at room temperature when temperature reaches to 150 degrees C. The Ce3+ and Tb3+ co-doped NBCP phosphor is a promising candidate for the application in the general lighting and display fields. (c) 2021 Chinese Society of Rare Earths. Published by Elsevier B.V. All rights reserved.

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