Abstract
In this work, we reported the results of photoluminescent and structural investigations of Gd3+/Tb3+ co-doped silicate xerogels as well as derivative SiO2-LaF3 nano-glass-ceramics. The molar ratio of appropriate acetates used during the synthesis, i.e., La(AcO)3:Gd(AcO)3:Tb(AcO)3 was fixed to x:(0.95-x):0.05. Based on XRD measurements, the crystallization of hexagonal LaF3 nanophase was verified without any admixture of GdF3 phase, even for samples with La3+:Gd3+ molar ratio ≤1. The optical characterization of fabricated Gd3+/Tb3+ co-doped sol-gel materials involved the registration and analysis of photoluminescence excitation (PLE) and emission spectra (PL), as well as the decay curves for the 6P7/2 (Gd3+) and the 5D4 (Tb3+) excited levels. Upon excitation at λex = 275 nm wavelength, the fabricated sol-gel samples revealed the series of emission lines assigned to the electronic transitions from both dopants, i.e., Gd3+ and Tb3+, indicating apparently the occurrence of Gd3+/Tb3+ energy transfer process (ET). The photoluminescence measurements comprehensibly proved the competitiveness between Gd3+ and Tb3+ ions to be entered into LaF3 fluoride nanocrystal lattice, formed during annealing of as-prepared xerogels. Based on the recorded PL spectra for fabricated sol-gel samples, some chromatic parameters were calculated, i.e., chromaticity coordinates (CIE), correlated color temperatures (CCT), and color purities (CP). The prepared Gd3+,Tb3+ co-doped samples are able to emit green light with CCT values in a range from 5967 K to 6291 K, and high CP reached 70 %, which predispose them for use as efficient constituents for developing green-emitting devices.
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