Abstract

Single-phase Dy3+-doped zinc gallate (ZnGa2O4) phosphors were synthesized using a conventional solid-state fabrication technique. The structural properties of the host phosphor were determined through X-ray powder diffraction (XRPD) and Rietveld refinement, revealing a cubic spinal structure with a space group of Fd3m. The reflectance properties of the host and doped samples were measured using UV–Vis spectroscopy. The obtained data were used to estimate the bandgap of all the synthesized samples, ranging from 4.18 to 3.69 eV, confirming the formation of a wide bandgap semiconductor. Morphological, compositional, and surface mapping analyses were conducted using a field emission scanning electron microscope, energy dispersive electron spectroscopy, and time-of-flight secondary ion mass spectroscopy. X-ray photoelectron spectroscopy was employed to confirm the oxidation state of the constituent elements and for an in-depth study of the crystal structure. Photoluminescence excitation and emission spectra were recorded to analyze the luminescent properties of the synthesized phosphors. It was confirmed that when using an excitation wavelength of 247 nm, all samples exhibited broad host emission with decreasing intensity. In contrast, Dy3+ emission displayed an increasing trend, confirming host sensitization in this phosphor. To analyze the radiative properties of the activator ion, theoretical analysis using the Judd-Ofelt theory was carried out. The results revealed an overlapping of orbitals between the O2− ion and Dy3+, indicating its higher-order covalent nature and the increased symmetric nature of the activator ion in the present host. This characteristic allowed for the generation of near-white light emissions. A concentration of 7 mol% of Dy3+ was observed to match well with achromatic white (0.32, 0.33) on the color chromaticity diagram. The luminous properties of this material suggest that it is a desirable candidate for use in LEDs and AC electroluminescent systems.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call