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Borogermanate glasses singly doped with Dy3+ ions were synthesized and then studied using the absorption and luminescence spectra. Spectroscopic changes of Dy3+ ions have been examined for compositional-dependent glasses with various molar ratios GeO2:B2O3. In this work, several spectroscopic parameters of Dy3+ ions were obtained experimentally and compared to the calculated values from the Judd–Ofelt theory. Luminescence spectra measured for borogermanate glasses consist of blue, yellow and red bands, which correspond to 4F9/2 → 6H15/2, 4F9/2 → 6H13/2 and 4F9/2 → 6H11/2 transitions of Dy3+, respectively. Luminescence lifetimes for the 4F9/2 excited state are reduced, whereas the stimulated emission cross-sections for the most intense 4F9/2 → 6H13/2 yellow transition of Dy3+ increase with increasing GeO2 and decreasing B2O3 concentrations in glass-hosts. Quantum efficiency of the 4F9/2 (Dy3+) excited state is nearly independent on molar ratios GeO2:B2O3. Attractive spectroscopic properties related to the 4F9/2 → 6H13/2 transition of Dy3+ ions are found for borogermanate glasses implying their potential utility for yellow laser action and solid-state lighting technology. [ABSTRACT FROM AUTHOR]

Kowalska et al. [[17]] report near-IR luminescence properties of selected rare-Earth ions (Er SP 3+ sp , Pr SP 3+ sp , Ho SP 3+ sp , Tm SP 3+ sp ) in titanate-germanate glasses under excitation of Yb SP 3+ sp . 35683100 17 Kowalska K., Kuwik M., Pisarska J., Pisarski W.A. Near-IR luminescence of rare-earth ions (Er3+, Pr3+, Ho3+, Tm3+) in titanate-germanate glasses under excitation of Yb3+. Rare-Earth ions, as optically active ions, are usually incorporated into the crystalline phases. [Extracted from the article]

Er3+-doped glass based on TiO 2 –GeO 2 –BaO–Ga 2 O 3 has been examined for mid-IR luminescence applications. Mid-IR luminescence corresponding to the 4I 11/2 → 4I 13/2 transition of Er3+ is enhanced in the presence of TiO 2. These effects are stronger for mid-IR emission at 2727 nm than near-IR emission at 1533 nm related to the 4I 13/2 → 4I 15/2 transition of Er3+. The gain bandwidth for the 4I 11/2 → 4I 13/2 transition of Er3+ is relatively large (σ em × FWHM = 8.14 × 10−26cm3), which imply that glass with TiO 2 might be a promising candidate for efficient sources emitting mid-IR radiation. • Titanate-germanate glass doped with Er3+ has been studied for mid-IR emission. • Mid-IR luminescence at 2700 nm is enhanced significantly in the presence of TiO 2. • The relatively large gain bandwidth for the 4I 11/2 → 4I 13/2 transition of Er3+ is observed. [ABSTRACT FROM AUTHOR]

Blue and green luminescence spectra of Tb3+ ions in lead phosphate glasses were examined under UV excitation. The green-to-blue luminescence intensity ratio G/B is considerably reduced with decreasing Tb3+ concentration. Thus, blue emission lines are enhanced in comparison to the main 5D4-7F5 green transition of Tb3+. These effects strongly depend on terbium-terbium interactions in lead phosphate glasses. It was confirmed by luminescence decay curve analysis and calculations using the Inokuti-Hirayama model. [ABSTRACT FROM AUTHOR]

Up-conversion luminescence of Er 3+ -doped oxyfluoride germanate optical fiber is observed under laser-diode excitation. The enhanced green emission line is due to 2 H 11/2 , 4 S 3/2  →  4 I 15/2 transition of Er 3+ . The integrated luminescence intensity related to 2 H 11/2 , 4 S 3/2  →  4 I 15/2 (green) and 4 F 9/2  →  4 I 15/2 (red) transitions of Er 3+ is reduced with increasing temperature. Several spectroscopic parameters of Er 3+ ions in optical fibers were determined. The spectral linewidth is reduced, whereas the maximum of emission peak is shifted to longer wavelengths with increasing fiber length. [ABSTRACT FROM AUTHOR]

Temperature-dependent up-conversion luminescence spectra of Er 3+ in lead-free germanate glass have been examined under 800 nm and 980 nm diode laser excitation. Green up-conversion luminescence spectra measured in the 500–580 nm ranges correspond to transitions originating from thermally coupled 2 H 11/2 and 4 S 3/2 levels to 4 I 15/2 ground level of Er 3+ . The relative emission band intensities of 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ are changed with temperature. The rate of fluorescence intensity ratio varying with temperature was calculated for glass sample excited at 800 nm and 980 nm, respectively. The maximum temperature sensitivity is nearly 20% higher for glass sample pumped at 980 nm than 800 nm. [ABSTRACT FROM AUTHOR]

Green and red up-conversion luminescence spectra corresponding to 2 H 11/2 , 4 S 3/2 → 4 I 15/2 and 4 F 9/2 → 4 I 15/2 transitions of Er 3+ ions in Er 3+ /Yb 3+ co-doped lead-free fluorogermanate glasses have been examined as a function of Yb 3+ concentration and temperature. The green-to-red luminescence intensity ratio diminishes with increasing Yb 3+ concentration. The luminescence intensity ratio for bands related to the 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ was determined and temperature sensitivity parameters were calculated. The maximal temperature sensitivities for Er 3+ /Yb 3+ co-doped glass samples increase with increasing Yb 3+ concentration and the highest value of 42.5 × 10 −4 K −1 at room temperature was obtained for 0.5Er-3Yb system. Based on gathered data it was concluded that Er 3+ /Yb 3+ co-doped lead-free fluorogermanate glasses are promising for optical temperature sensing. [ABSTRACT FROM AUTHOR]

Er 3+ /Yb 3+ co-doped lead germanate glasses have been examined for up-conversion luminescence temperature sensors. Up-conversion luminescence spectra corresponding to 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ are changed with temperature. The fluorescence intensity ratio (FIR) and temperature sensitivity were determined. The maximum sensitivity is found to be 70 × 10 −4 K −1 at T = 550 K in the temperature range of 300–600 K. It suggests that Er 3+ /Yb 3+ co-doped lead germanate glass is promising for optical temperature sensors. [ABSTRACT FROM AUTHOR]

Excitation and emission spectra of Pr 3+ :PLZT ceramics have been studied. Several emission bands were measured under blue laser excitation, which correspond to 3 P 0 → 3 H 4 , 1 D 2 → 3 H 4 , 3 P 0 → 3 H 4 and 3 P 0 → 3 F 2 transitions of trivalent Pr 3+ . Their integrated emission intensities were determined. The blue-to-red luminescence intensity ratios of Pr 3+ depend significantly on free sintering/hot pressing methods used for PLZT fabrication and activator concentration. Luminescence decay curves for the 1 D 2 state of Pr 3+ :PLZT ceramics are also presented and discussed. [ABSTRACT FROM AUTHOR]

Up-conversion luminescence spectra of Er 3+ ions in PbO–Ga 2 O 3 –GeO 2 and PbO–Ga 2 O 3 –SiO 2 glasses have been examined as a function of temperature in the 298–650 K range. The relative emission intensities of green bands corresponding to 2 H 11/2 → 4 I 15/2 and 4 S 3/2 → 4 I 15/2 transitions of Er 3+ were determined with temperature. Based on up-conversion luminescence spectra of Er 3+ , the fluorescence intensity ratio and temperature sensitivity for glasses based on PbO–Ga 2 O 3 –XO 2 (X = Ge, Si) were calculated. The maximum sensitivity is equal to 20.4 × 10 − 4 K − 1 at T = 620 K (X = Ge) and 26.4 × 10 − 4 K − 1 at T = 590 K (X = Si) suggesting potential application in optical sensor thermometry. [ABSTRACT FROM AUTHOR]

Luminescence properties of Pr 3+ ions in germanate glasses modified by BaF 2 were investigated. Several luminescence bands originating to transitions from the 3 P 0 state to the lower-lying states of Pr 3+ were registered under 450 nm excitation. The spectral analysis suggests that the positions of luminescence bands and their relative intensities are changed significantly with BaF 2 content. The relative integrated luminescence intensities of 3 P 0 → 3 H 4 transition (blue) to the 3 P 0 → 3 F 2 transition (red) of Pr 3+ ions strongly depend on fluoride modifier BaF 2 in glass composition. The luminescence bands of Pr 3+ ions are shifted to shorter wavelengths with increasing BaF 2 content. [ABSTRACT FROM AUTHOR]

The glass structure, photoluminescence properties of Eu 3+ , Judd–Ofelt analysis, and near infrared emissions of Er 3+ at 1.5 μm in the oxyfluoride glasses and glass–ceramics of 1Eu 2 O 3 - or 1Er 2 O 3 -doped 50BaF 2 – x Al 2 O 3 –(50 − x )B 2 O 3 ( x = 0–25 mol%) were investigated. It was clarified on the ground of Raman scattering spectroscopy and F1s and O1s XPS measurements that the glass with no Al 2 O 3 (1Er 2 O 3 –50BaF 2 –50B 2 O 3 ) is composed of BO 3 , BO 2 F and BO 3 F units with F–Ba bonds. The glasses with 25Al 2 O 3 (1Er 2 O 3 –50BaF 2 –25Al 2 O 3 –25B 2 O 3 ) is mainly composed of BO 3− and Al(O,F) x units. Existence of non-bridging oxygen was not detected by O1s-XPS spectra. It was proposed that these structures are largely affected on crystallization behavior, e.g., the glass with no Al 2 O 3 forms BaF 2 and β -BaB 2 O 4 due to Ba–F bonds and the glass with 25Al 2 O 3 forms BaAlBO 3 F 2 because the glass structure composed of BO 3 and Al(O,F) units is similar to the BaAlBO 3 F 2 crystal structure. Judd–Ofelt parameters of Er 3+ and Eu 3+ in the glasses showed almost the same values in Ω 4 and Ω 6 for each glass, on the other hand Ω 2 decreased with addition of Al 2 O 3 . The emission spectra of Er 3+ at 1.5 μm in the glasses and glass–ceramics with BaAlBO 3 F 2 crystals showed broad peaks. It is proposed that oxyfluoride glasses and glass–ceramics based on the BaF 2 –Al 2 O 3 –B 2 O 3 system have a high potential for optical device applications such as broadband optical amplifiers. [ABSTRACT FROM AUTHOR]

Lead bismuth gallate glasses doped with Eu 3+ and Dy 3+ ions were examined using excitation and luminescence measurements. From excitation spectrum of Eu 3+ ions the electron–phonon coupling strength and phonon energy of the glass host was calculated. Strong luminescence quenching of Dy 3+ and enhancement of Eu 3+ is well observed, which is due to presence of Bi 3+ → Eu 3+ and Dy 3+ → Bi 3+ energy transfer processes in lead bismuth gallate glass. Luminescence decay analysis and calculations based on Inokuti–Hirayama model confirms this hypothesis. [ABSTRACT FROM AUTHOR]

Lead-free oxyfluoride borate glasses singly doped with Pr 3+ and Er 3+ were prepared and next investigated using absorption and luminescence spectroscopy. In the studied glass system, barium oxide was substituted by BaF 2 . Two luminescence bands of Pr 3+ located at visible spectral region are observed, which correspond to 3 P 0 – 3 H 4 (blue) and 1 D 2 – 3 H 4 (reddish orange) transitions, respectively. The luminescence bands due to 1 D 2 – 3 H 4 transition of Pr 3+ are shifted to shorter wavelengths, when BaO was substituted by BaF 2 . Near-infrared luminescence spectra of Er 3+ ions in lead-free borate glasses modified by BaF 2 correspond to 4 I 13/2 – 4 I 15/2 transition. Their spectral linewidths increase with increasing BaF 2 concentration. The changes in measured lifetimes of rare earth ions are well correlated with the bonding parameters calculated from the optical absorption spectra. [ABSTRACT FROM AUTHOR]

Thermal, structural and optical properties of lead phosphate glasses containing Er 3+ ions have been studied as a function of PbF 2 concentration. Incorporation of PbF 2 results in structural and spectroscopic changes around Er 3+ ions and surrounding ligands, which were analyzed in detail using by DSC, XRD, absorption and luminescence spectroscopy. Especially, near-infrared luminescence spectra due to main 4 I 13/2 - 4 I 15/2 laser transition of Er 3+ ions are presented and discussed with PbF 2 content. Based on decay curve measurements the 4 I 13/2 luminescence lifetime of Er 3+ was determined and its value is found to be maximum at 18 mol% of PbF 2 . [ABSTRACT FROM AUTHOR]

Spectroscopic properties of rare earths in lead-free oxyfluoride germanate glasses were studied. The absorption and luminescence spectra of Eu 3+ , Pr 3+ and Er 3+ ions were examined as a function of BaF 2 concentration and several spectroscopic parameters for rare earths were determined. The ratio of integrated luminescence intensity of the 5 D 0 → 7 F 2 transition to that of the 5 D 0 → 7 F 1 transition of Eu 3+ decrease significantly with increasing BaF 2 content. The absorption (Er 3+ ) and emission (Pr 3+ ) ‘hypersensitive transitions’ of rare earths are shifted in direction to shorter wavelengths with increasing BaF 2 content in glass composition. Emission spectra and their decays corresponding to the main 4 I 13/2 → 4 I 15/2 laser transition of Er 3+ were also analyzed. Quite long-lived NIR luminescence of Er 3+ is observed for lead-free glass samples with low BaF 2 concentration. [ABSTRACT FROM AUTHOR]

Spectroscopic properties of Er 3+ ions in lead-free oxyfluoride germanate glasses were studied. The absorption and luminescence spectra of Er 3+ ions were examined for glass samples with low and high BaF 2 content. From absorption spectra the bonding parameter was calculated and its value is reduced with increasing BaF 2 content. The maximum of absorption peak due to 4 I 15/2 − 2 H 11/2 hypersensitive transition is shifted to shorter wavelengths (blue shift) with increasing BaF 2 content. Luminescence spectra and their decays corresponding to main 4 I 13/2 − 4 I 15/2 laser transition of Er 3+ are also presented and discussed. Quite long-lived near-infrared luminescence of Er 3+ is observed for lead-free glass samples with low BaF 2 concentration. [ABSTRACT FROM AUTHOR]

Highlights: [•] Lead phosphate glasses doped with rare earth ions were prepared. [•] The local structure was examined using X-ray diffraction and spectroscopic methods. [•] Different structural phosphate groups are present in lead phosphate glasses. [•] The electron–phonon coupling strength and phonon energy of the glass host was determined. [•] Several observed emission bands are due to 4f–4f electronic transitions of rare earth ions. [ABSTRACT FROM AUTHOR]

Abstract: Structural and optical properties of Eu3+ and Dy3+ ions in PbO–Ga2O3–XO2 (X=Te, Ge, Si) glasses have been examined using X-ray diffraction, FT-IR and luminescence spectroscopy. Several crystalline phases such as TeO2, PbTe3O7, PbO and PbO2 were identified in lead tellurite system using X-ray diffraction analysis, in contrast to PbO–Ga2O3–XO2 (X=Ge, Si) glass samples. Characteristic emission bands due to the 5D0 → 7F J (J =0–4) transitions of Eu3+ and the 4F9/2 → 6H J /2 (J =15, 13, 11) transitions of Dy3+ were registered. Two spectroscopic parameters, such as luminescence intensity ratios associated to 5D0 → 7F2 and 5D0 → 7F1 transitions of Eu3+ as well as 4F9/2 → 6H13/2 and 4F9/2 → 6H15/2 transitions of Dy3+, and luminescence lifetimes for excited states of rare earth ions were determined. The luminescence intensity ratios for Eu3+ and Dy3+ ions decrease, whereas 5D0 (Eu3+) and 4F9/2 (Dy3+) luminescence lifetime increases, when covalence between Ln3+ and O2− ions is reduced and the phonon energy of the host glass is increased in PbO–TeO2 →PbO–GeO2 →PbO–SiO2 direction. It was confirmed by FT-IR measurements. [Copyright &y& Elsevier]

Abstract: Luminescence of lead bismuthate glasses PbO-Bi2O3-Ga2O3 containing Dy3+ ions has been studied. Two overlapping luminescence bands corresponding to 3P1–1S0 transition of Bi3+ and 4F9/2 –6H13/2 transition of Dy3+ were detected under 480nm excitation. Comparison of luminescence features for the system under study to those reported for dysprosium-doped lead borate glass PbO-B2O3-Ga2O3 indicates that the luminescence of Dy3+ is efficiently quenched by Bi3+ ions. Analysis of luminescence dynamics implies that the excitation energy transfer from Dy3+ to Bi3+ is nonradiative. The theoretical calculations using Inokuti–Hirayama model confirm strong luminescence of Dy3+ ions in lead bismuthate glasses. [Copyright &y& Elsevier]

Abstract: Selected heavy metal glasses containing Yb3+ and Er3+ ions have been studied. Near-infrared luminescence spectra at 1.53μm and up-conversion spectra of Er3+ ions were registered under excitation of Yb3+ ions by 975nm diode laser line. The luminescence bands correspond to 4I13/2–4I15/2 (NIR), 4S3/2–4I15/2 (green) and 4F9/2–4I15/2 (red) transitions of Er3+, respectively. The optical transitions of rare earth ions have been examined as a function of glass host. The unusual large spectral linewidth nearly close to 110nm for 4I13/2–4I15/2 transition of Er3+ ions in Yb–Er co-doped lead borate glass was obtained, whereas long-lived NIR luminescence at 1.53μm was detected in lead germanate glass. The NIR luminescence and up-conversion phenomena strongly depend on stretching vibrations of glass host, which was confirmed by FT-IR spectroscopy. [Copyright &y& Elsevier]

Abstract: Ln-doped oxychloride lead borate glasses were studied using luminescence spectroscopy. Rare earth ions were limited to trivalent Pr3+, Tm3+, Eu3+ and Er3+. Luminescence spectra were registered, which correspond to 3P0–3H4 and 1D2–3H4 transitions of Pr3+, 1G4–3H5 and 1G4–3F4 transitions of Tm3+, 5D0–7F J (J=0, 1, 2, 3, 4) transitions of Eu3+ and 4S3/2,2H11/2–4I15/2 and 4I13/2–4I15/2 transitions of Er3+. Luminescence decays from the excited states of Ln3+ ions were analyzed in detail. The experimental results indicate that relatively high phonon energy of the host gives important contribution to the excited state relaxation of rare earth ions. [Copyright &y& Elsevier]

Abstract: The spectroscopic and laser properties of Nd3+ and Dy3+ ions in lead borate glass were studied. Luminescence spectra recorded in the near-infrared and visible ranges correspond to 4F3/2–4I J /2 (J=9, 11, 13) transitions of Nd3+ and 4F9/2–6H J /2 (J=11, 13, 15) transitions of Dy3+, respectively. Luminescence decay curves were analyzed as a function of activator concentration. Luminescence quenching is observed, which is due to Ln–Ln interaction increasing. Several spectroscopic parameters relevant to laser potential of Ln3+ ions (Ln=Nd, Dy) in lead borate glass were determined. The relatively large values of the quantum efficiency and the room-temperature emission cross-section for the 4F3/2–4I11/2 transition of Nd3+ at 1061nm and the 4F9/2–6H13/2 transition of Dy3+ at 573nm imply that Ln-doped lead borate glasses can be considered as promising solid-state materials for laser applications. [Copyright &y& Elsevier]

Abstract: Influence of rare earth ions on structural behavior in lead borate glasses has been investigated using infrared spectroscopy. The structural changes have been analyzed with increasing rare earth concentration. Partial BO3↔BO4 conversion as a function of rare earth concentration is observed only for the smaller heavier lanthanides, whereas for the larger lighter lanthanides the concentration effect has not been found. [Copyright &y& Elsevier]

Abstract: Spectroscopic analysis of Pr3+ and Er3+ ions in fluoride and oxide systems belonging to the same heavy metal glass family has been reported. From absorption and emission spectra using Judd–Ofelt theory various spectroscopic parameters like radiative transition rates, luminescence lifetimes, radiative quantum efficiencies, spectral line widths as well as emission cross-sections are determined. Selected examples for the spectroscopic behavior of both optical glasses are discussed in relation to the practical application of these materials as a potential laser-active media in the visible and infrared spectral region. [Copyright &y& Elsevier]

The effect of erbium concentration on thermal stability and quantum efficiency of excited states was studied using DSC, XRD and optical methods. A large value of stability parameter ΔT close to 118 °C has been obtained for fluoroindate glass singly doped with 2 mol% of erbium ions. With increasing erbium concentration stability parameter extremely decreased and several crystalline peaks appeared, what was stated by X-ray diffraction. Also, the strong luminescence quenching is observed. This behavior is consistent with nonradiative processes related to the Er–Er interaction. [Copyright &y& Elsevier]

This paper deals with broadband near-infrared luminescence properties of lead germanate glass triply doped with Yb3+/Er3+/Tm3+. Samples were excited at 800 nm and 975 nm. Their emission intensities and lifetimes depend significantly on Er3+ and Tm3+ concentrations. For samples excited at 800 nm, broadband emissions corresponding to the overlapped 3H4 → 3F4 (Tm3+) and 4I13/2 → 4I15/2 (Er3+) transitions centered at 1.45 µm and 1.5 µm was identified. Measurements of decay curves confirm reduction of 3H4 (Tm3+), 2F5/2 (Yb3+) and 4I13/2 (Er3+) luminescence lifetimes and the presence of energy-transfer processes. The maximal spectral bandwidth equal to 269 nm for the 3F4 → 3H6 transition of Tm3+ suggests that our glass co-doped with Yb3+/Er3+/Tm3+ is a good candidate for broadband near-infrared emission. The energy transfer from 4I13/2 (Er3+) to 3F4 (Tm3+) and cross-relaxation processes are responsible for the enhancement of broadband luminescence near 1.8 µm attributed to the 3F4 → 3H6 transition of thulium ions in lead germanate glass under excitation of Yb3+ ions at 975 nm. [ABSTRACT FROM AUTHOR]

In this work, spectroscopic properties of europium and erbium ions in heavy metal oxide glasses have been studied. The phonon energy of the glass host was determined based on Eu3+ excitation spectra measurements. Near-IR emission spectra at 1550 nm related to 4I13/2 → 4I15/2 transition of erbium in heavy metal glasses were examined with special regards to luminescence bandwidth and measured lifetime. In particular, correlation between phonon energy and the measured lifetime 4I13/2 (Er3+) was proposed. The luminescence lifetime for the 4I13/2 upper laser state of erbium decreases with increasing phonon energy in glass matrices. Completely different results were obtained glass samples with europium ions, where the 5D0 lifetime increases with increasing phonon energy. Our investigations suggest that the values of measured 5D0 lifetime equal to radiative lifetimes for all heavy metal oxide glasses. [ABSTRACT FROM AUTHOR]

Fluoroindate glasses co-doped with Pr3+/Er3+ ions were synthesized and their near-infrared luminescence properties have been examined under selective excitation wavelengths. For the Pr3+/Er3+ co-doped glass samples several radiative and nonradiative relaxation channels and their mechanisms are proposed under direct excitation of Pr3+ and/or Er3+. The energy transfer processes between Pr3+ and Er3+ ions in fluoroindate glasses were identified. In particular, broadband near-infrared luminescence (FWHM = 278 nm) associated to the 1G4 → 3H5 (Pr3+), 1D2 → 1G4 (Pr3+) and 4I13/2 → 4I15/2 (Er3+) transitions of rare earth ions in fluoroindate glass is successfully observed under direct excitation at 483 nm. Near-infrared luminescence spectra and their decays for glass samples co-doped with Pr3+/Er3+ are compared to the experimental results obtained for fluoroindate glasses singly doped with rare earth ions. [ABSTRACT FROM AUTHOR]

Novel multicomponent titanate-germanate glasses singly doped with transition metal (Cr3+) and rare earth ions (Eu3+) were synthesized and the glass transition temperatures and thermal stability parameters were determined using DSC measurements. X-ray diffraction analysis confirmed fully amorphous nature of the received samples. Their structural and optical properties were compared with germanate glasses without TiO2. Correlation between local structure and optical properties in titanate-germanate glasses is well evidenced by FT-IR, Raman, EPR, and luminescence spectroscopy. In particular, luminescence spectra and their decays are examined for glass samples, where GeO2 was partially substituted by TiO2. [ABSTRACT FROM AUTHOR]

Lead tungstate PbWO4 nanocrystals in transparent lead borate glass-ceramics containing Er3+ ions were fabricated. Luminescence spectra at about 1530 nm due to main 4 I13/2-4 I15/2 laser transition of Er3+ ions were examined for glass samples before and after heat treatment. Near-infrared luminescence of Er3+ ions in glass-ceramics is enhanced and long-lived in comparison to precursor glasses. It suggests that the Er3+ ions are partially incorporated into PbWO4 crystalline phase. [ABSTRACT FROM AUTHOR]

Abstract: Transparent glass-ceramics were successfully prepared during controlled heat treatment of lead borate glasses. The PbF2 particles were dispersed into a borate glass matrix which was evidenced by X-ray diffraction analysis. The phase identification revealed that crystalline peaks can be related to the orthorhombic PbF2 phase. Green up-conversion luminescence due to the 4S3/2–4I15/2 transition of Er3+ ions was registered. In comparison to the precursor glass the luminescence intensity was considerably higher, whereas the luminescence linewidth slightly decreased in the studied oxyfluoride transparent glass-ceramics. It indicated that apart of the trivalent erbium was incorporated into the PbF2 crystalline phase. [Copyright &y& Elsevier]

Abstract: Near-infrared luminescence spectra at 1.53μm due to main 4I13/2–4I15/2 laser transition of Er3+ ions in oxide and oxyhalide lead borate glasses were examined. Spectroscopic parameters like spectral linewidth and luminescence lifetime were analyzed with PbX2 (X=F, Cl or Br) doping. An introduction of lead halide to the borate glass results in the reduction of spectral linewidth and the increase of luminescence lifetime of Er3+. The luminescence decay from the 4I13/2 upper state of Er3+ is longer for glass sample with PbF2 than PbX2 (X=Cl or Br). [Copyright &y& Elsevier]

In this paper, we report on fabricating optical fibers with a controlled process of crystallization core during the drawing process. The research and synthesis of the core material of silica-germanium-antimony oxide glass were discussed. We also investigated the optical and luminescence properties were in relation to concentrating Eu 2 O 3 and P 2 O 5. Based on this investigation, we selected the most promising material for optical fiber core. In the next step, we drew optical fibers using a well-known rod-in-tube method. After drawing, we examine the optical fibers for luminescence shape changes. We observed a promising similarity between optical fibers and heat-treated samples with confirmed nanocrystals. Finally, XRD and TEM measurements confirm EuPO 4 nanocrystals at the core of the optical fiber. Highlighting the successful control of crystallization in the one-step method used to draw optical fibers. [ABSTRACT FROM AUTHOR]

Transparent Yb3+/Er3+ glass-ceramic was successfully obtained by the extrusion method. The extrusion of oxyfluoride tellurite-germanate glass co-doped with Yb3+ and Er3+ ions at 520 ℃ resulted in the formation of Ba0.75Er0.25F2.25 nanocrystals, leading to an increase in the upconversion (UC) emission intensity of 35 times in glass-ceramic with respect to the glass. The glass to glass-ceramic transition was confirmed by X-ray diffraction (XRD) and Transmission electron microscope (TEM). Also, the structural changes that occurred during crystallization were assessed using Fourier-transform infrared (FTIR) spectroscopy. Furthermore, the pump power and temperature UC emission dependence of glass and glass-ceramic under 976 nm laser excitation were investigated in detail. The assessments showed that i) two-phonons are involved in the UC process and ii) the temperature has a significant influence over it. The Yb3+/Er3+ codoped glass-ceramic shows relatively high Sa and Sr values in a wide temperature range from 300 to 573 K, presenting the maximal Sa value of 3.50 × 10-3 at 573 K and the maximal Sr value of 6.30 × 10-3 at 364 K. These results suggest that the glass-ceramic is a good candidate for optical applications such as luminescent thermometry. [ABSTRACT FROM AUTHOR]

LMA (Large Mode Area) optical fibers are presently under active investigation to explore their potential for generating laser action or broadband emission directly within the optical fiber structure. Additionally, a wide mode profile significantly reduces the power distribution density in the fiber cross-section, minimizing the power density, photodegradation, or thermal damage. Multi-stage deposition in the MCVD-CDT system was used to obtain the structural doping profile of the LMA fiber multi-ring core doped with Tm3+ and Tm3+/Ho3+ layer profiles. The low alumina content (Al2O3: 0.03wt%) results in low refractive index modification. The maximum concentrations of the lanthanide oxides were Tm2O3: 0.18wt % and Ho2O3: 0.15wt%. The double-clad construction of optical fiber with emission spectra in the eye-safe spectral range of (1.55–2.10 µm). The calculated LP01 Mode Field Diameter (MFD) was 69.7 µm (@ 2000 nm, and 1/e of maximum intensity), which confirms LMA fundamental mode guiding conditions. The FWHM and λmax vs. fiber length are presented and analyzed as a luminescence profile modification. The proposed structured optical fiber with a ring core can be used in new broadband optical radiation source designs. [ABSTRACT FROM AUTHOR]

In this study, a comprehensive analysis of emission in erbium-doped and erbium and ytterbium co-doped fluoroindate glasses has been presented. The luminescence of the erbium transitions and the effect of ytterbium co-doping under 488, 808 and 976 nm laser excitation have been discussed. Optimization of rare-earth (RE) ions doping concentration and the energy transfer processes related to the sensibilization effect in Er3+/Yb3+ co-doped fluoroindate glasses focusing on the reciprocal distribution of radiative transitions, energy transfer parameters, and lifetimes have been analyzed. The luminescence consists of several bands in the visible (525, 546 and 660 nm) and the infrared (1550 and 2700 nm) spectral regions that correspond to characteristic radiative energy transitions within the erbium ions. In glasses co-doped with the Er3+/Yb3+ system, an augmentation in the emission intensity was observed in the visible and at 1550 nm, while a decrease was observed in the 2700 nm infrared band. The increase of the Yb3+: 2F 5/2 lifetime under 488, 808 and 976 nm excitation showed significant Er3+: 4I 11/2 → Yb3+: 2F 5/2 back energy transfer. Based on the analysis of the available literature, it can be concluded that energy transfer upconversion and cooperative energy upconversion play a significant role in modulating luminescence intensity values within the examined emission bands. This effect is likely enhanced due to the incorporation in a low phonon energy glass matrix. As a result of the above optimization, a glass optical fiber co-doped with 0.8 YbF 3 /1.4 ErF 3 (in mol%) was drawn and characterized, showing a strong emission at 2.77 μm. The optimized Er3+/Yb3+ co-doped fluoroindate glass and glass optical fiber confirmed their ability to be used in the visible and near-infrared spectral regions as efficient optical fiber sources. [ABSTRACT FROM AUTHOR]

In this work, Tm3+ doped and Tm3+/Ho3+ co-doped germanate glasses with various TiO 2 concentrations have been examined using optical spectroscopy. The broad emission bands corresponding to 3F 4 →3H 6 (1.8 μm) and 5I 7 →5I 8 (2 μm) transitions of thulium and holmium ions were registered, respectively. It was observed that the intensity of near-infrared emission bands significantly changes with increasing titanium oxide content in the glass composition. Furthermore, the energy transfer process from Tm3+ to Ho3+ ions in studied glass systems was confirmed and discussed. The dependence of spectroscopic parameters like full width at half maximum (FWHM) and energy transfer efficiency (η ET) on increased TiO 2 concentration in glass host was established. [ABSTRACT FROM AUTHOR]

In this contribution a comprehensive spectroscopic study of Dy3+ doped fluoroindate glass samples and glass fiber is presented. The mid-infrared (MIR) emission from DyF 3 doped bulk glass samples (0.2, 0.4, 0.8, 1.2, 1.4, 1.6 mol.%) is investigated when pumping at 1320 nm. A broadband mid-infrared emission spanning from 2800 nm to 3500 nm with 0.88 ms emission lifetime of the 6H 13/2 level in 0.2 mol.% glass sample was observed. Also 0.2 mol.% of DyF 3 doped fluoroindate glass fiber was drawn and its photoluminescence properties were studied showing the emission spectrum to 3500 nm and the 6H 13/2 level lifetime of 0.91 ms. The results obtained show that fluoroindate glass is a good candidate for further development of tunable fiber lasers and broadband mid-infrared spontaneous emission fiber sources. [ABSTRACT FROM AUTHOR]

This work presents an analysis of the spectroscopic properties of glass and glass ceramics co-doped with Ni2+ and Er3+ ions. Spectroscopic analysis showed the embedding of nickel ions in the gamma-gallium oxide nanocrystals as a result of heat treatment of the glass samples. Analysis of the luminescence properties of the obtained samples under 940 nm and 980 nm pump excitation allowed the selection of a proper Er3+ ions concentration for further optical fiber fabrication. Measured lifetime results of glass-ceramics samples confirm energy transfer from nickel ions to erbium. In the process of drawing the optical fiber, it was possible to create a transparent nanocrystalline glass-ceramic core, as confirmed by XRD results. The produced glass-ceramic optical fiber was characterized by broadband emission in the range from 1100 nm to 1650 nm corresponding to the 3T 2 (3F) →3A 2 (3F) (Ni2+) and 4I 13/2 → 4I 15/2 (Er3+) transitions for 940 nm and 980 nm pump excitation. The Er3+ to Ni2+ ions emission intensity ratio of the fabricated glass-ceramic fiber was estimated to be 0.84 and 7.14 for 940 nm and 980 nm optical pumps, respectively. [ABSTRACT FROM AUTHOR]

In this work, the series of silicate xerogels co-doped with Gd3+ and Eu3+ ions have been synthesized via a sol-gel method and further processed into nano-glass-ceramic materials. The mutual molar ratio of trivalent metal ions' acetates in samples' compositions was gradually modified as follows: La3+:Gd3+:Eu3+ = (0.95-x):x:0.05, x = 0.05, 0.25, 0.45, 0.65, and 0.90; hence the molar ratio of Gd3+:Eu3+ (R Gd/Eu) was set from 1 through 5, 9, 13 up to 18. XRD measurements confirmed the amorphous nature of fabricated xerogels, but their heat-treatment successfully triggered the crystallization of hexagonal LaF 3 fraction with an average size of about ∼10 nm, which was additionally confirmed by HR-TEM microscopy. Additionally, it was found that the LaF 3 phase crystallized in a whole range of proposed La(CH 3 COO) 3 :Gd(CH 3 COO) 3 molar ratio, and Gd3+ ions played only the role of dopant and replaced La3+ cation in the fluoride crystal lattice. The optical characterization of prepared sol-gel samples involved the registration of absorption, excitation and emission spectra, along with the luminescence decay analysis from the 6P 7/2 (Gd3+) and the 5D 0 (Eu3+) excited states. For nano-glass-ceramics defined by R Gd/Eu = 13 and 18, the unexpected prolongation of the τ(6P 7/2):Gd3+ lifetimes was denoted, compared with samples singly-doped with Gd3+. The changes in photoluminescence behavior of studied samples are strongly dependent on the nature of the fabricated sol-gel samples, the established molar ratios of La3+:Gd3+:Eu3+, and the tendency of cation-exchange in LaF 3 nanocrystal lattice by Gd3+ and Eu3+ ions. [ABSTRACT FROM AUTHOR]

Near‐infrared (NIR) luminescence of Pr3+ and Tm3+ ions in titanate‐germanate glasses has been studied for laser and fiber amplifier applications. The effect of the molar ratio GeO2:TiO2 (from 5:1 to 1:5) on spectroscopic properties of glass systems was studied by absorption, luminescence measurements, and theoretical calculations using the Judd–Ofelt theory. It was found that independent of the TiO2 concentration, intense NIR emissions at 1.5 and 1.8 μm were observed for glasses doped with Pr3+ and Tm3+ ions, respectively. Moreover, several spectroscopic and NIR laser parameters for Pr3+ and Tm3+ ions, such as emission bandwidth, stimulated emission cross‐section, quantum efficiency, gain bandwidth, and figure of merit, were determined. The results were discussed in detail and compared to the different laser glasses. Systematic investigations indicate that Pr3+‐doped system with GeO2:TiO2 = 2:1 and Tm3+‐doped glass with GeO2:TiO2 = 1:2 present profit laser parameters and could be successfully applied to NIR lasers and broadband optical amplifiers. [ABSTRACT FROM AUTHOR]

Double-clad optical fiber with a multi-ring core profile doped with thulium and holmium fabricated by Modified Chemical Vapor Deposition Chelate Doping Technology (MCVD-CDT) is presented. The measured Tm2O3 and Ho2O3 complexes' weight concentrations were 0.5% and 0.2% respectively. Numerical analyses show weakly guiding conditions and 42.2 µm of MFD LP01 at 2000 nm. The low NA numerical aperture (NA = 0.054) was obtained for the 20/250 µm core/cladding ratio optical fiber construction. The emission spectra in the range of 1.6–2.1 µm vs. the fiber length are presented. The full width at half maximum (FWHM) decreases from 318 to 270 nm for fiber lengths from 2 to 10 m. The presented fiber design is of interest for the development of new construction of optical fibers operating in the eye-safe spectral range. [ABSTRACT FROM AUTHOR]

Double-clad optical fiber with a multi-ring core profile doped with thulium and holmium fabricated by Modified Chemical Vapor Deposition Chelate Doping Technology (MCVD-CDT) is presented. The measured Tm2O3 and Ho2O3 complexes' weight concentrations were 0.5% and 0.2% respectively. Numerical analyses show weakly guiding conditions and 42.2 µm of MFD LP01 at 2000 nm. The low NA numerical aperture (NA = 0.054) was obtained for the 20/250 µm core/cladding ratio optical fiber construction. The emission spectra in the range of 1.6–2.1 µm vs. the fiber length are presented. The full width at half maximum (FWHM) decreases from 318 to 270 nm for fiber lengths from 2 to 10 m. The presented fiber design is of interest for the development of new construction of optical fibers operating in the eye-safe spectral range. [ABSTRACT FROM AUTHOR]

An investigation of fluoroindate glass and fiber co-doped with Yb3+/Er3+ ions as a potential temperature sensor was assessed using the fluorescence intensity ratio (FIR) technique. Analysis of thermally coupled levels (TCLs—2H11/2 and 4S3/2), non-thermally coupled levels (non-TCLs—4F7/2 and 4F9/2), and their combination were examined. Additionally, the luminescent stability of the samples under constant NIR excitation using different density power at three different temperatures was carried out. The obtained values of absolute sensitivity (0.003 K−1—glass, 0.0019 K−1—glass fiber 2H11/2 → 4S3/2 transition) and relative sensitivity (2.05% K−1—glass, 1.64% K−1—glass fiber 4F7/2 → 4F9/2 transition), as well as high repeatability of the signal, indicate that this material could be used in temperature sensing applications. [ABSTRACT FROM AUTHOR]

Nanophosphors are widely used, especially in biological applications in the first and second biological windows. Currently, nanophosphors doped with lanthanide ions (Ln3+) are attracting much attention. However, doping the matrix with lanthanide ions is associated with a narrow luminescence bandwidth. This paper describes the structural and luminescence properties of co-doped LaPO4 nanophosphors, fabricated by the co-precipitation method. X-ray structural analysis, scanning electron microscope measurements with EDS analysis, and luminescence measurements (excitation 395 nm) of LaPO4:Eu3+/Nd3+ and LaPO4:Eu3+/Nd3+/Yb3+ nanophosphors were made and energy transfer between rare-earth ions was investigated. Tests performed confirmed the crystal structure of the produced phosphors and deposition of rare-earth ions in the structure of LaPO4 nanocrystals. In the range of the first biological window (650–950 nm), strong luminescence bands at the wavelengths of 687 nm and 698 nm (5D0 → 7F4:Eu3+) and 867 nm, 873 nm, 889 nm, 896 nm, and 907 nm (4F3/2 → 4I9/2:Nd3+) were observed. At 980 nm, 991 nm, 1033 nm (2F5/2 → 2F7/2:Yb3+) and 1048 nm, 1060 nm, 1073 nm, and 1080 nm (4F3/2 → 4I9/2:Nd3+), strong bands of luminescence were visible in the 950 nm–1100 nm range, demonstrating that energy transfer took place. [ABSTRACT FROM AUTHOR]

Modified barium gallo-germanate glass hosts are still worthy of attention in studying structure–property relationships. In this work, two different series of glass systems based on (60-x)GeO2-xTiO2-30BaO-10Ga2O3 and (60-x)GeO2-xB2O3-30BaO-10Ga2O3 (x = 10, 30, 50 mol%) were synthesized, and their properties were studied using spectroscopic techniques. X-ray diffraction (XRD) patterns revealed that all fabricated glasses were fully amorphous material. The absorption edge shifted toward the longer wavelengths with a gradual substitution of GeO2. The spectroscopic assignments of titanium ions were performed with excitation and emission spectra compared to the additional sample containing an extremely low content of TiO2 (0.005 mol%). On the basis of Raman and FT-IR investigations, it was found that increasing the TiO2 content caused a destructive effect on the GeO4 and GeO6 structural units. The Raman spectra of a sample containing a predominantly TiO2 (50 mol%) proved that the band was located near 650 cm−1, which corresponded to the stretching vibration of Ti-O in TiO6 unit. The deconvoluted IR results showed that the germanate glass network consisted of the coexistence of two BO3 and BO4 structural groups. Based on the experimental investigations, we concluded that the developed materials are a promising candidate for use as novel glass host matrices for doping rare-earth and/or transition metal ions. [ABSTRACT FROM AUTHOR]

The near-infrared luminescence properties of Pr3+/Yb3+: PLZT ferroelectric ceramics have been examined for the first time. Independently, upon either 450 nm (Pr3+) or 980 nm (Yb3+) excitation, luminescence centered at 1340 nm was observed, which corresponds to the 1G4→3H5 transition of Pr3+. Several spectroscopic parameters for the 1G4→3H5 transition of Pr3+ ions were determined. The average product of emission cross section and radiative lifetime were relatively large for all x/65/35 PLZT samples ( x=6-10) studied, with values close to 105±2 (×10−26 cm2·s). These spectroscopic investigations indicate that Pr3+/Yb3+: PLZT ferroelectric ceramics are promising candidate for efficient sources emitting near-infrared radiation at 1340 nm. [ABSTRACT FROM AUTHOR]

The sol-gel powders doubly-doped with Gd 3+ /Eu 3+ ions with different concentration of Gd 3+ have been successfully obtained. The spectroscopic characterization of prepared samples was conducted based on excitation and emission spectra as well as luminescence decay analysis. Upon direct excitation of Eu 3+ active ions, the characteristic 5 D 0 → 7 F 1 (orange) and 5 D 0 → 7 F 2 (red) emission bands were observed. The energy transfer from Gd 3+ to Eu 3+ ions was registered upon λ exc = 273 nm excitation. An efficient conversion of ultraviolet radiation (UV) into visible luminescence was successfully observed. The energy transfer process from Gd 3+ to Eu 3+ led to longer luminescence decay from the 5 D 0 state in comparison to that obtained under direct excitation of Eu 3+ ions (λ exc = 393 nm). Generally, obtained results clearly indicated the beneficial influence of increasing concentration of Gd 3+ ions on luminescence properties of Eu 3+ in studied silica sol-gel phosphors. [ABSTRACT FROM AUTHOR]

In this paper, the effect of the GeO2:TiO2 molar ratio in glass composition on the spectroscopic properties of germanate glasses was systematically investigated. The visible luminescence bands associated with characteristic 1D2 → 3H4 (red), 5S2, 5F4 → 5I8 (green), and 1D2 → 3F4 (blue) transitions of Pr3+, Ho3+, and Tm3+ ions in systems modified by TiO2 were well observed, respectively. It was found that the luminescence intensity of glasses containing Pr3+ and Ho3+ ions increases, whereas, for Tm3+-doped systems, luminescence quenching with increasing content of TiO2 was observed. Based on Commission Internationale de I'Eclairage (CIE) chromaticity coordinates (x, y) analysis, it was demonstrated that the value of chromaticity coordinates for all glasses depends on the GeO2:TiO2 molar ratio. The addition of TiO2 to system compositions doped with Tm3+ ions shifts the (x, y) to the center of the CIE diagram. However, chromaticity coordinates evaluated for glasses containing Pr3+ ions move to a purer red color. Our results confirm that the spectroscopic properties of the studied glasses strongly depend on TiO2 content. Moreover, it can be stated that germanate-based glass systems modified by TiO2 can be used for optoelectronics in RGB technology as red (Pr3+), green (Ho3+), and blue (Tm3+) emitters. [ABSTRACT FROM AUTHOR]