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- W2899698311 abstract "Li2O-BaO-Gd2O3-SiO2 glasses with different concentration of Eu3+ ions were developed by the traditional melt quenching technique and characterized via FTIR, absorption, excitation, emission and CIE color coordinates analysis for visible red emission application. The FTIR shows strong band at position 740 cm−1 which is attributed to Si-O-Si symmetric stretching mode. Density and molar volume of LBGSEu glasses increases with Eu3+ ions concentration. The covalent nature of bond between the Eu3+ ions and surrounding ligands was confirmed from the bonding parameter (δ). From absorption spectra JO-parameters and oscillator strength are evaluated for LBGSEu6 glass. From JO-parameters, Eu3+ ions have asymmetric coordination environment and stronger covalency. The phonon line PSB (22,522 cm−1) confirm the phonon energy ≈971 cm−1, that corresponds to the energy of one phonon associated with maximum energy of the vibrational mode couple to Eu3+ ions. Under 275 nm and 393 nm excitation, intense red emission was observed at 613 nm, we observe efficient energy transfer phenomena from Gd3+ → Eu3+ in these glasses. Increasing trend of IR with increasing concentration of Eu2O3 indicates the asymmetric environment around Eu3+ ions in LBGS. Moreover, from JO analysis, LBGS glasses have high capability for red laser device with high lasing power and energy extraction ratio. The fluorescence lifetimes show decreasing trend in lifetime with increasing concentration of Eu2O3 is due to radiative transition. From CIE color coordinate, the CIE color coordinates of LBGSEu6 glass fall in reddish region close to orange region and can be useful for optical display devices." @default.
- W2899698311 created "2018-11-16" @default.
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- W2899698311 date "2019-03-01" @default.
- W2899698311 modified "2023-10-17" @default.
- W2899698311 title "Energy transfer phenomenon of Gd3+ to excited ground state of Eu3+ ions in Li2O-BaO-Gd2O3-SiO2-Eu2O3 glasses" @default.
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- W2899698311 doi "https://doi.org/10.1016/j.saa.2018.11.008" @default.
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