Enhanced luminescence of Eu in LaAlBO via energy transfer from Dy doping.

Spectrochim Acta A Mol Biomol Spectrosc

Jazan University, College of Science, Department of Physical Sciences, Physics Division, P.O. Box 114, 45142 Jazan, Saudi Arabia; Nanotechnology Research Unit, College of Science, Jazan University, P.O. Box. 114, Jazan 45142, Saudi Arabia. Electronic address:

Published: November 2024


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Article Abstract

In this study, an investigation was conducted on the structural and photoluminescence (PL) characteristics of LaAlBO (LAB) phosphors initially incorporated with Dy and Eu ions. Subsequently, the impact of varying Eu concentration while maintaining a constant Dy concentration was examined. Structural characterization was performed using X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), and energy-dispersive X-ray spectroscopy (EDS). XRD analysis confirmed the effective embedding of both dopants into the hexagonal framework of the LAB. The PL emission spectra revealed characteristic emissions of Dy (blue and yellow) and Eu (red) ions. The optimized dopant concentrations of both Dy and Eu were observed to be 3 wt%. The dominant mechanism for concentration quenching in doped LAB phosphors was determined to be the electric dipole-dipole interaction. Co-doping with Eu led to a substantial decrease in Dy emission intensity (∼0.18-fold) while enhancing Eu emission intensity (∼3.72-fold). The critical energy transfer distance (R = 11.64 Å) and the analysis based on the Dexter theory confirmed that the energy transfer mechanism corresponds to dipole-dipole interaction. The color purities and correlated color temperatures (CCT) were estimated, suggesting the potential of these phosphors for warm white and red lighting applications, respectively. The observed energy transfer and luminescence properties, along with the structural and compositional characterization, highlight the promising potential of LAB:Dy/Eu co-doped phosphors for advanced lighting and display technologies.

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http://dx.doi.org/10.1016/j.saa.2024.124711DOI Listing

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