Issue 38, 2023

Crystal structural and photoluminescence properties of Eu3+ doped MgZn2(PO4)2 phosphors by R+ (R = Li, Na, K) charge compensation

Abstract

Eu3+ single doping and Eu3+, R+ (R = Li, Na, K) charge compensation co-doped orange-red MgZn2(PO4)2 phosphors were prepared by high-temperature solid-state method. The effect of charge compensation agent R+ on the luminescence properties of MgZn2(PO4)2:Eu3+ phosphors was investigated. The morphology and composition of the samples were characterized using X-ray diffraction (XRD), high-resolution transmission electron microscopy (HRTEM), high-angle annular dark field (HAADF), and energy dispersive spectroscopy (EDS) techniques. The photoluminescence properties were studied using excitation and emission spectra. In this study, R+ is used as charge compensation to improve the emission intensity of Eu3+ and the physical explanation is given. The optimal doping concentration of Eu3+ in MgZn2(PO4)2 was obtained to be 5 mol%. Under ultraviolet (396 nm) excitation, a strong orange-red luminescence corresponding to the 5D07Fi (i = 1, 2, 3, and 4) transition of Eu3+ is observed. The CIE coordinates and decay lifetimes of typical samples are discussed. The chromaticity coordinates of the two samples were (0.604, 0.392) and (0.616, 0.382), respectively, both located in the orange-red region. The fluorescence lifetime of MgZn2(PO4)2 phosphors co-doped 5% Eu3+ and 5% R+ (R = Na and K) is obviously improved. The results show that MgZn1.9R0.05(PO4)2:0.05Eu3+ (R = Na and K) is a kind of orange-red phosphor with high efficiency under near ultraviolet excitation.

Graphical abstract: Crystal structural and photoluminescence properties of Eu3+ doped MgZn2(PO4)2 phosphors by R+ (R = Li, Na, K) charge compensation

Article information

Article type
Paper
Submitted
22 Jul 2023
Accepted
24 Aug 2023
First published
28 Aug 2023

CrystEngComm, 2023,25, 5436-5443

Crystal structural and photoluminescence properties of Eu3+ doped MgZn2(PO4)2 phosphors by R+ (R = Li, Na, K) charge compensation

Y. Huang, Z. Liu, Y. Xiong and W. Feng, CrystEngComm, 2023, 25, 5436 DOI: 10.1039/D3CE00729D

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