Issue 3, 2023

Structure, photoluminescence properties, and energy transfer phenomenon in Sm3+/Eu3+ co-doped CaTiO3 phosphors

Abstract

Sm3+-doped and Sm3+/Eu3+ co-doped CaTiO3 phosphor samples were synthesized by solid-state reaction method and characterized using XRD, FE-SEM, FTIR, XPS, UV visible absorption, and photoluminescence techniques. All the compounds showed a crystalline structure with an orthorhombic phase and Pnma(62) space group. The diffuse reflectance spectra showed an absorption band due to the host along with peaks for Sm3+ and Eu3+ ions. The photoluminescence emission spectra of Sm3+-doped CaTiO3 phosphor showed orange-red and deep red emissions on excitation with 407 nm in which the peak at 599 nm was of maximum intensity. Similarly, Eu3+ ions showed a maximum intensity peak at 613 nm on excitation with 398 nm wavelength. The Sm3+/Eu3+ co-doped CaTiO3 phosphor showed an energy transfer from Sm3+ to Eu3+ ions on excitation with 407 nm and the nature of interaction between them was found to be dipole–dipole type. The CIE color coordinates and the correlated color temperature (CCT) calculations of the phosphors were performed, which showed an orange-red color emission useful for LED applications. The lifetime of Sm3+ ions decreases in the presence of Eu3+ ions and this was due to energy transfer from Sm3+ to Eu3+ ions. The temperature-dependent PL spectra of the phosphors showed thermal quenching behaviour. The activation energy of CaTiO3:2Sm3+, CaTiO3:2.5Eu3+, and CaTiO3:2Sm3+/2.5Eu3+ phosphors were found to be 0.27, 0.22, and 0.17 eV, respectively.

Graphical abstract: Structure, photoluminescence properties, and energy transfer phenomenon in Sm3+/Eu3+ co-doped CaTiO3 phosphors

Article information

Article type
Paper
Submitted
24 Nov 2022
Accepted
03 Dec 2022
First published
20 Dec 2022

New J. Chem., 2023,47, 1460-1471

Structure, photoluminescence properties, and energy transfer phenomenon in Sm3+/Eu3+ co-doped CaTiO3 phosphors

P. Singh, H. Mishra, P. C. Pandey and S. B. Rai, New J. Chem., 2023, 47, 1460 DOI: 10.1039/D2NJ05774C

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