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Abstract

A series of CaY2Al4SiO12:xEu3+ (x = 0.01, 0.03, 0.05, 0.07 and 0.09) phosphors were synthesized by the sol–gel method. X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM) and energy dispersive spectroscopy (EDS) techniques were used in the study of the crystal structure, surface morphology, and elemental composition of the prepared phosphors. Photoluminescence (PL) and thermoluminescence (TL) properties were also studied. When the CaY2Al4SiO12:Eu3+ phosphor was excited at 394 nm wavelength, the optimum emission peak centered at 592 nm was found. The calculated CIE coordinates from the PL emission spectra lie in the orange-red region of the visible spectrum. To determine the optimum doping concentration of Eu3+ , the variation in the luminescence intensity with different concentrations of Eu3+ in the CaY2Al4SiO12 host lattice was also studied. To study the TL of the prepared samples, a 60Co- γ (gamma) source was used for irradiation and to determine the trapping parameters such as activation energy (E), order of kinetics (b) and frequency factor (s) of the samples, Chen’s peak shape method was used.

Details

Title
Luminescence Studies of CaY2Al4SiO12:Eu3+ Phosphor by Sol–Gel Method
Author
Verma, Anita 1   VIAFID ORCID Logo  ; Sharma, Ravi 2 ; Bisen, D. P. 1 ; Brahme, Nameeta 1 ; Richhariya, Tripti 3 ; Tiwari, Kanchan 4 ; Thakkar, Kamlesh 1 

 Pt. Ravishankar Shukla University, SoS in Physics and Astrophysics, Raipur, India (GRID:grid.440705.2) (ISNI:0000 0001 2190 6678) 
 Government Arts and Commerce Girls College, Department of Physics, Raipur, India (GRID:grid.440705.2) 
 Kalinga University, Department of Physics, Raipur, India (GRID:grid.472298.2) 
 Government Nagarjuna Post Graduate College of Science, Department of Physics, Raipur, India (GRID:grid.472298.2) 
Pages
6769-6777
Publication year
2023
Publication date
Oct 2023
Publisher
Springer Nature B.V.
ISSN
0361-5235
e-ISSN
1543-186X
Source type
Scholarly Journal
Language of publication
English
ProQuest document ID
2859761545
Copyright
© The Minerals, Metals & Materials Society 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.