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Publishing Language: Chinese | Open Access

Preparation and Characterization of Double Perovskite Sr2GdSbO6:Eu3+ Phosphor

Zhi-xiong Fang, Shuang-ping Yi( ), Yi-xuan Zhou, Wei-ren Zhao
School of Physics and Optoelectronic Engineering, Guangdong University of Technology, Guangzhou 510006, China
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Abstract

The Sr2GdSbO6:Eu3+ red phosphor with double perovskite structure was successfully prepared by high temperature solid phase method and its XRD, photoluminescence spectrum and fluorescence decay lifetime were characterized. The XRD of the Sr2Gd0.8SbO6:0.2Eu3+ phosphor is basically consistent with the peak position of the standard card, indicating that the doping of Eu3+did not change the crystal structure of the matrix. The crystal parameters after Rietveld refinement also verify the result. The photoemission spectrum shows that the sample has a wide excitation area centered at 340 nm in the ultraviolet region; under the excitation of a 340 nm light source, the strongest emission of the sample is an orange-red emission band with a center wavelength of 593 nm. Using Dexter theory to analyze the concentration quenching mechanism of the sample is the dipole-dipole interaction. The fluorescence decay life of Sr2Gd0.8SbO6:0.2Eu3+ phosphors at room temperature is 4.202 ms, and the external quantum efficiency is 24.8%. When the temperature is raised to 150 ℃, the external quantum efficiency remains 68.8% of that at room temperature. The calculated color purity of Sr2GdSbO6:Eu3+ phosphor can reach 99.5%. Sr2Gd0.8SbO6:0.2Eu3+ phosphor, blue phosphor, green phosphor and 365 nm UV chip package were made into LED devices which can emit bright white light. These results indicate that Sr2GdSbO6:Eu3+ phosphor is a potential red phosphor for white LED.

CLC number: O482.31

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Journal of Guangdong University of Technology
Pages 88-94

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Cite this article:
Fang Z-x, Yi S-p, Zhou Y-x, et al. Preparation and Characterization of Double Perovskite Sr2GdSbO6:Eu3+ Phosphor. Journal of Guangdong University of Technology, 2023, 40(2): 88-94. https://doi.org/10.12052/gdutxb.210008

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Received: 12 January 2021
Published: 01 March 2023
© 2023 Editorial Office of Journal of Guangdong University of Technology

This is an open access article under the CC BY-NC-ND license (https://creativecommons.org/licenses/by-nc-nd/4.0/).