Issue 23, 2024

Cool green-emissive Y2Si2O7:Tb3+ nanophosphor: auto-combustion synthesis and structural and photoluminescence characteristics with good thermal stability for lighting applications

Abstract

A cheap, versatile, sustainable and energy-efficient gel-combustion method was applied to develop a series of green-emitting down-converted Y2Si2O7:Tb3+ (YPS:Tb3+) nanophosphors. Employing XRD-based Rietveld refinement approach, the phase purity and crystallographic evaluation of the produced phosphor were conducted, revealing a triclinic crystal with P[1 with combining macron] space group. EDX and TEM analyses were performed on the synthesized samples to determine their elemental composition and morphological properties. Diffuse reflectance spectra yielded 5.61 eV and 5.79 eV optical energy band gaps for the host and the optimized (0.04 mole of Tb3+) sample, respectively. UV light has the ability to excite the nanocrystalline phosphor in an efficient manner, leading to significant luminosity qualities attributed to the radiative relaxation of 5D47FJ (J = 6, 5, 4, 3). The bi-exponential decay function was derived by the PL decay curves. With an activation energy of 0.2206 eV, the Y1.96Si2O7:0.04Tb3+ phosphor exhibits good thermal quenching capabilities. Improved photometric attributes including CIE coordinates, CCT and color purity confirmed the green glow, indicating a strong competitor for cool-green emission in lighting applications.

Graphical abstract: Cool green-emissive Y2Si2O7:Tb3+ nanophosphor: auto-combustion synthesis and structural and photoluminescence characteristics with good thermal stability for lighting applications

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Article information

Article type
Paper
Submitted
05 Apr 2024
Accepted
26 Apr 2024
First published
22 May 2024
This article is Open Access
Creative Commons BY-NC license

RSC Adv., 2024,14, 16560-16573

Cool green-emissive Y2Si2O7:Tb3+ nanophosphor: auto-combustion synthesis and structural and photoluminescence characteristics with good thermal stability for lighting applications

P. Kumar, D. Singh, S. Kadyan, H. Kumar and R. Kumar, RSC Adv., 2024, 14, 16560 DOI: 10.1039/D4RA02571G

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