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Glasses doped with lanthanides ions may be good white light emitters due to their interesting physical and spectroscopic properties. In this paper, the optical spectroscopy of rare earths doped glasses with a special emphasis on application as white LED were presented. The luminescent glass materials containing Ln3+ (Ln = Pr, Tb, Dy) and Ce3+ ions were obtained. The glasses samples were prepared by a traditional melt-quenching technique. The optical properties of glasses containing various concentrations of rare earth ions were analyzed. It was observed that luminescence bands corresponding to characteristic transitions of Ln3+ and cerium ions are present on spectra measured under direct excitation of Ce3+. Therefore, it indicates that the energy transfer process between Ce3+/Pr3+, Ce3+/Tb3+, Ce3+/Dy3+ ions in glasses occurs. Some parameters such as correlated color temperature (CCT) and chromaticity coordinates (CIE) that characterize white LEDs were analyzed and discussed in detail. [ABSTRACT FROM AUTHOR]

Heavy metal oxide and oxyfluoride lead silicate glasses doped with rare-earth ions were prepared. Next, they were heat treated in order to obtain transparent glass-ceramics. The rare-earths as optically active ions were limited to trivalent Eu3+ and Dy3+. Correlation between the local structure and the luminescence properties of Eu3+ and Dy3+ ions in the studied glass and glass-ceramic systems was examined using X-ray diffraction, FT-IR and optical measurements. Especially, the ratio of integrated emission intensity of the 5D0--7F2 transition to that of the 5D0--7F1 transition of Eu3+, defined as the luminescence intensity ratio R (Eu3+) as well as the ratio of integrated emission intensity of the 4F9/2--6H13/2 transition to that of the 4F9/2--6H15/2 transition of Dy3+, defined as the luminescence intensity ratio Y/B (Dy3+), have been analyzed in details. Their values are reduced due to part incorporation of rare-earth ions into cubic β-PbF2 crystalline phase. The excitation and luminescence spectra of rare-earth ions in glass samples before and after heat treatment are presented and discussed in relation to potential application in optoelectronics. [ABSTRACT FROM AUTHOR]

Heavy metal lead borate glasses doped with rare earth ions were examined. The influence of heavy metal oxide PbO and activator concentration on luminescence properties of rare earth ions are discussed. Rare earth ions were limited to Eu3+, Dy3+ and Tb3+ which are emitting in the visible light. Increasing concentration of lead oxide in relation to boron oxide causes an increase in R (Eu3+), Y/B (Dy3+) and G/B (Tb3+) spectroscopic factors which correspond to the relative integrated luminescence intensities of 5D0-7F2/5D0-7F1, 4F9/2-6H13/2/4F9/2-6H15/2 and 5D4-7F5/5D4-7F6 transitions, respectively. Moreover, the influence of heavy metal oxide and activator concentration on luminescence decays from excited states of rare earth ions was examined in details. [ABSTRACT FROM AUTHOR]

Oxychloroborate glasses containing Dy3+ ions in the B2O3-PbCl2-PbO-Al2O3-WO3 system were studied using X-ray diffraction, Raman, FT-IR, absorption, excitation and luminescence spectroscopy. The results concerning glass preparation, short-range order structure and optical properties are reported. X-ray diffraction analysis evidently indicates that the fully amorphous system was prepared. Coexistence of trigonal BO3 and tetrahedral BO4 units was evidenced by Raman and FT-IR spectroscopy. The electronic states belonging to the 4f 9 configuration of trivalent Dy3+ were determined from the absorption and excitation spectra. The luminescence bands at 480, 573 and 662 nm were registered in oxychloride glasses, which correspond to transitions originating from the 4F9/2 state to the 6HJ/2 (J = 11, 13, 15) states of Dy3+. [ABSTRACT FROM AUTHOR]

Oxyhalide lead borate glasses doped with rare earth ions have been studied before and after thermal treatment. The rare earths as optically active ions were limited to the Er3+ ions. Near-infrared luminescence due to the main 4I13/2-4I15/2 laser transition of Er3+ was registered. The introduction of PbX2 to the borate glass results in a reduction of spectral linewidth and an increase of luminescence lifetime of 4I13/2 state of Er3+ ions. The unusual large spectral linewidth for 4I13/2-4I15/2 transition of Er3+ in the oxide glass host was obtained, whereas the luminescence decay from 4I13/2 state is longer for a sample with PbF2 than PbCl2 and PbBr2. Heat treatment introduces transformation from a glass to transparent glass-ceramic (TGC). The coordination sphere around Er3+ ions is changed, giving important contribution to the luminescence characteristics. The spectroscopic consequence of this transformation is the increase of luminescence lifetime and the narrowing of spectral lines of Er3+. [ABSTRACT FROM AUTHOR]

Oxyfluoride lead borate glasses singly doped with Nd3+ and Er3+ ions have been studied before and after thermal treatment. The orthorhombic PbF2 crystallites are formed during thermal treatment, which was evidenced by X-ray diffraction analysis. Near-infrared luminescence spectra at 1.06 µm and 1.53 µm have been registered for samples before and after annealing, which correspond to the main 4F3/2-4I11/2 and 4I13/2-4I15/2 laser transitions of Nd3+ and Er3+ ions, respectively. Luminescence decays from 4F3/2 state of Nd3+ and 4I13/2 state of Er3+ have been analyzed in detail. Contrary to Nd-doped samples, the luminescence lines obtained for Er-doped transparent oxyfluoride glass-ceramics are more intense and narrowed, whereas the luminescence decays from 4I13/2 state of Er3+ are slightly longer in comparison to precursor glasses. [ABSTRACT FROM AUTHOR]

Energy transfer processes from Cr3+ to Nd3+ and NIR luminescence of Nd3+ ions at 1.06 µm in Cr-Nd co-doped lead borate glasses have been investigated. The spectroscopic investigation indicates that Cr3+ ions are located at strong-field and weak-field sites. Replacing PbO by PbF2 in lead borate glasses slightly influences the energy transfer processes between Cr3+ and Nd3+ and NIR luminescence of Nd3+ ions. The energy transfer process occurs in both oxide and oxyfluoride glass systems, which may be due to the thermally induced population of the 4T2 excited state of Cr3+ ions and the participation of lattice phonons. [ABSTRACT FROM AUTHOR]

Energy transfer processes in lead borate glasses doubly doped with Yb-Tm and Yb-Er have been investigated at room temperature under excitation of Yb at 975 nm. The non-resonant energy transfer from ²F5/2 state of Yb to ³H5 state of Tm results in up-converted emission at 850 nm due to the ³H4-³H6 transition of thulium ions. The nearly resonant transfer from ²F5/2 state of Yb to 4I11/2 state of Er results in green up-conversion and near-infrared emission, which correspond to the 4S3/2-4I15/2 and 4I13/2-4I15/2 transitions of erbium ions, respectively. High Yb concentration in both co-doped samples is required for optimal energy transfer efficiency (η > 90%). Results with the singly Yb-doped samples are also presented to clarify the energy transfer process. [ABSTRACT FROM AUTHOR]