Issue 41, 2023

NaGdF4:Eu3+ nanocrystalline: an in-depth study of energy transfer processes and Judd–Ofelt analysis using the luminescence excitation spectrum

Abstract

NaGdF4 nanocrystalline doped with different concentrations of Eu3+ ions were synthesized using the precipitation method. The structure and morphology of the material were investigated through the measurements of the XRD patterns and SEM images, respectively. The optical properties of the NaGdF4:Eu3+ nanocrystalline were studied in the framework of the Judd–Ofelt theory in which the Ωλ parameters were calculated by two methods: the traditional method using the luminescence spectra and the self-referenced method using the luminescence excitation spectra. In NaGdF4:Eu3+ nanocrystalline, the Gd3+ ions in the lattice act as sensitizer centers for the luminescence of Eu3+ ions under excitation at 272 and 310 nm. The energy transfer process from Gd3+ to Eu3+ causes the emission enhancement of Eu3+ ions. Upon excitation by the characteristic wavelengths of Gd3+, the luminescence efficiency of the Eu3+ ions in NaGdF4:Eu3+ is affected by two mechanisms: the emission of Gd3+ ions and the trapping of excited energy by the Eu3+ ions. The energy transfer between Eu3+ ions was also discussed in detail. This process leads to the enhancement of the luminescence bands originating from the 5D0 level. The dominant interaction between the Eu3+ ions in the energy transfer process is the dipole–dipole mechanism, which is determined by fitting the decay curve of the 5D2 level to the Inokuti–Hirayama model.

Graphical abstract: NaGdF4:Eu3+ nanocrystalline: an in-depth study of energy transfer processes and Judd–Ofelt analysis using the luminescence excitation spectrum

Article information

Article type
Paper
Submitted
28 May 2023
Accepted
25 Sep 2023
First published
26 Sep 2023

Phys. Chem. Chem. Phys., 2023,25, 28296-28308

NaGdF4:Eu3+ nanocrystalline: an in-depth study of energy transfer processes and Judd–Ofelt analysis using the luminescence excitation spectrum

P. Van Do, N. X. Ca, L. D. Thanh, D. D. Quan, N. M. Hung, P. Tien Du, N. Thi Huong and D. T. Anh, Phys. Chem. Chem. Phys., 2023, 25, 28296 DOI: 10.1039/D3CP02458J

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