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Crystals of Gd3Al2.5Ga2.5O12:Er3+, (Lu0.3Gd0.7)2SiO5:Er3+ and LiNbO3:Er3+ compounds differing in origin and the nature of their inherent structural disorder were crystalized. Optical absorption and luminescence spectra for transitions between the 4I15/2 and the 4I13/2 multiplets of Er3+ ions for the crystal samples were recorded versus temperatures in the region of 80–300 K. Gathered data were analyzed thoroughly providing the in-depth knowledge of the effects of temperature on intensities, wavelengths and bandwidths of Er3+ transitions. The information acquired together with the knowledge of significant structural dissimilarities of the host crystals chosen made it possible to propose an interpretation of the impact of a structural disorder in Er3+-doped crystals on their spectroscopic properties, and to determine their lasing ability at cryogenic temperatures upon resonant (in-band) optical pumping. [ABSTRACT FROM AUTHOR]

Novel ternary fluoro-germano-tellurite (GTS) glasses doped with Er3+ ions with 0.5 mol% and 1.0 mol% were fabricated by a conventional melt and quenching method and investigated using methods of optical spectroscopy. The room-temperature absorption spectrum was recorded and analyzed to determine radiative transition rates, radiative lifetimes, and branching ratios of Er3+ luminescence. Decay curves of Er3+ luminesccence were recorded and analyzed. Temperature dependences of emission spectra and absorption spectra in the region from RT (room-temperature) up to 675 K were studied in detail. The contribution of competing radiative and nonradiative processes to the relaxation of luminescent levels of Er3+ was assessed. Absolute and relative sensitivity were established utilizing the comprehensive model based on thermally coupled 2H11/2/4S3/2 excited states of erbium. The high quantum efficiency of the first erbium-excited state and value of gain coefficient indicate that GTS:Er glass system can be considered as conceivable NIR (near infrared) laser material as well. [ABSTRACT FROM AUTHOR]

Detailed spectroscopic investigation of YVO 4 :5 at% Eu 3+ , 1 at % Tm 3+ single crystal encompassing analysis of absorption, excitation and time resolved emission spectra recorded at 5 K and 300 K made it possible to determine energies, intensities and bandwidths of transitions within 4f n configurations of trivalent thulium and europium. Transients recorded upon femtosecond pulse excitation made it possible to determine dynamics of population build-up and relaxation of excited states involved in luminescence phenomena. It was found that in YVO 4 :Eu, Tm system the metastable 5 D 0 level of Eu 3+ and 1 G 4 level of Tm 3+ can be populated by energy transfer from excited VO 4 3− group and respective intra-ion relaxation processes from higher energy levels. Recorded excitation spectra of the 5 D 0 luminescence of Eu 3+ and of the 1 G 4 luminescence of Tm 3+ do not evidence the Eu 3+ ↔Tm 3+ energy transfer. Nevertheless, an examination of acquired luminescence decay curves, performed with reference to available information on relaxation dynamics of YVO 4 :Tm 3+ system, reveals that the incorporation of Eu 3+ accelerates decays of the 1 G 4 and 3 H 4 levels of Tm 3+ . Spectroscopic parameters characterising the donor–acceptor interaction involved in the 3 H 4 decay were evaluated applying the Inokuti–Hirayama model. Relevance of donor and acceptor transition peculiarities for energy transfer processes contributing to the 1 G 4 and 3 H 4 decays was assessed in the framework of phenomenological model proposed by Kushida and discussed. It was concluded that the intensity ratio of the blue 1 G 4 luminescence to orange–red 5 D 0 luminescence; hence the colour of visible emission in UV-excited YVO 4 :Eu 3+ , Tm 3+ phosphor, may be adjusted by appropriate choice of Eu 3+ and Tm 3+ concentrations. [ABSTRACT FROM AUTHOR]

Two single crystals of LGSO containing 1% Dy 3+ and differing in Ce 3+ concentration were grown by the Czochralski method. XRD examination revealed that a crystal with a nominal Ce 3+ concentration of 3% has the C2/c structure inherent to Lu 2 SiO 5 (LSO) whereas a crystal with a nominal Ce 3+ concentration of 1% has the P2 1 /c structure inherent to Gd 2 SiO 5 (GSO). In both crystal structure types the excitation of Ce 3+ ions is followed by an energy transfer to Dy 3+ ions and resulting visible emission consists of a broad-band Ce 3+ luminescence and of much more narrow bands of Dy 3+ luminescence. Excitation spectra imply that the efficiency of Dy 3+ excitation via Ce 3+ – Dy 3+ energy transfer is markedly higher than upon direct optical pumping into Dy 3+ excited levels. It was observed that visible emission in the two systems differs in spectral characteristics, hence in the colour of the emitted light. Examination of optical spectra recorded with a polarized light revealed important anisotropy of transition intensities of Ce 3+ ions in LGSO host with the P2 1 /c structure. [ABSTRACT FROM AUTHOR]

Highlights: [•] LGT:Er single crystals obtained by Czochralski method. [•] Analysis of absorption and emission spectra as well as decay curves of luminescence. [•] Influence of the temperature on the LGT:Er spectroscopic properties. [•] Spectroscopic evaluation of the LGT:Er potential laser qualities. [ABSTRACT FROM AUTHOR]

Abstract: Spectroscopic measurements of the calcium niobate CaNb2O6 single crystal doped with samarium ions were performed. Polarized absorption and emission spectra as well as luminescence decay curves of this material were recorded as a function of temperature in the 5–300K temperature region. Analysis of low temperature spectra made it possible to determine energies of crystal field components of Sm3+ multiplets involved in the excitation and luminescence phenomena. Number of crystal field levels derived implies that Sm3+ ions in the CaNb2O6 host are accommodated in several different sites. Radiative lifetime of the 4G5/2 metastable level determined based on the Judd–Ofelt analysis of room temperature absorption spectra amounts to 777μs, a value close to that of luminescence lifetime determined from luminescence decay curve. Energy transfer between the NbO6 group and samarium ions was observed in wide temperature range. Intense luminescence related to the 4G5/2→6H7/2 and 4G5/2→6H9/2 transitions centered at 610nm and 660nm, respectively, combined with strong absorption band near 404nm that matches perfectly the pump light provided by commercial InGaN/GaN diode lasers points at a potential of CaNb2O6:Sm3+ for the design of all-solid-state visible lasers. [Copyright &y& Elsevier]

Single crystal of LaGaTaO (LGT) containing intentionally 0.5 % of Ho and 1 % of Yb was grown by the Czochralski method. Examination of chemical composition of the grown crystal revealed that luminescent holmium and ytterbium ions are preferably retained in the melt and their actual concentrations are 0.12 and 0.24 %, respectively. Spectroscopic investigation performed encompassed IR host absorption spectra and Raman spectra at room temperature, optical absorption and luminescence spectra of Ho and Yb at room temperature and at 5 K, and luminescence decay curves at room temperature. It was found that all spectral bands recorded show important inhomogeneous line broadening. This feature was attributed to structural disorder inherent to the crystal lattice in which pentavalent Ta ions occupy octahedral Ga(1) sites together with trivalent Ga ions. Despite small concentrations of luminescent ions, the occurrence of nonradiative interaction that feeds the I and I levels of Ho ions by transfer of an excitation from the F level of Yb ions was evidenced. Based on examination of spectroscopic parameters evaluated, it was concluded that LGT:Ho, Yb may be considered as a potential intermediate-gain laser active material able to emit infrared radiation from the I → I transition of Ho around 2 micrometres upon laser-diode pumping into Yb absorption band. [ABSTRACT FROM AUTHOR]

A series of the Tb- and Dy-doped glasses with Li2O--2B2O3 (or Li2B4O7:Tb and Li2B4O7:Dy) composition were synthesised and their spectroscopic properties were investigated. The Li2B4O7:Tb and Li2B4O7:Dy glasses of high chemical purity and optical quality were obtained from corresponding polycrystalline compounds in the air using standard glass technology. The Tb and Dy impurities were added to Li2B4O7 composition in the form of Tb2O3 and Dy2O3 oxide compounds in amounts of 0.5 and 1.0 mol%. The electron paramagnetic resonance (EPR), luminescence excitation and emission spectra of the Li2B4O7:Tb and Li2B4O7:Dy glasses were investigated. On the basis of EPR and photoluminescence spectra analysis it was shown that the Tb and Dy impurities are incorporated in the Li2B4O7 glass network as Tb3+ (4f8, 7F6) and Dy3+ (4f 9, 6H15/2) ions, exclusively. All observed transitions of the Tb3+ and Dy3+ centres in the luminescence excitation and emission spectra were identified. The luminescence kinetics shows single exponential decay for Tb3+ and Dy3+ centres in Li2B4O7 glasses. The lifetime values for main emission transitions of the Tb3+ and Dy3+ centres in the Li2B4O7 glasses containing 0.5 and 1.0 mol% Tb2O3 and Dy2O3 are determined at T = 300 K. Peculiarities of optical properties and local structure of the Tb3+ and Dy3+ centres in the Li2B4O7:Tb and Li2B4O7:Dy glasses as well as their potential applications have been discussed. [ABSTRACT FROM AUTHOR]

Optical absorption, luminescence excitation, and emission spectra as well as luminescence kinetics of the Sm- and Yb-doped glasses with lithium tetraborate (Li2B4O7) composition were investigated and analysed. The Sm- and Yb-doped lithium tetraborate glasses of high optical quality were obtained in air from corresponding polycrystalline compounds according to standard glass synthesis technology. The Sm and Yb impurities were added to the Li2B4O7 compound in the form of Sm2O3 and Yb2O3 oxides in amount of 0.4 mol%. Using optical and electron paramagnetic resonance spectroscopy it was shown that the Sm and Yb impurities are incorporated into the lithium tetraborate glass network as Sm3+ (4f5, 6H5/2) and Yb3+ (4f13, 2F7/2) ions, exclusively. All of the observed transitions in the absorption and luminescence spectra of Sm3+ and Yb3+ centres were identified. The luminescence kinetics of the Sm3+ and Yb3+ centres in the Li2B4O7 glass are characterised by a single exponential decay. Decay constants for the main emission transitions of the Sm3+ and Yb3+ centres in the lithium tetraborate glass were obtained at T = 300 K. Incorporation peculiarities and optical spectra of Sm3+ and Yb3+ ions in the lithium tetraborate glass have been discussed in comparison with other borate glasses and crystals. [ABSTRACT FROM AUTHOR]

The 50GeO2-(50-x-y)PbO-yPbF2-xLnF3 glass single doped with Pr3+ and Tb3+ ions was studied. The composition of the material was modified by varying the content of both PbF2 (y = 5, 10, 15 mol%) and LnF3 (x = 0.2 and 2 mol%). The differential thermal analysis (DTA) of as-melted samples was used to determine thermal characteristics. Optical techniques and kinetics measurements were used to monitor the effect of thermal treatment on spectroscopic properties and dynamics of luminescent states of optically-active ions in amorphous and two-phase systems. It was found that non-exponential decays of praseodymium luminescence in as-melted material become exponential or nearly exponential with corresponding longer lifetimes in thermally-treated samples. This effect was not so strong in the Tb3+-doped glass. The influence of the PbF2 content on luminescence dynamics was studied for samples doped with 2 mol% of Pr3+. It was observed that the increase of PbF2 content leads to lengthening of luminescence lifetime, e.g., the 1D2 lifetime increases from 4.1 to 45 µs in 5 and 15 mol% of PbF2 as-melted samples, respectively. [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]

Optical absorption and luminescence spectra as well as luminescence kinetics of the Nd3+ centres in glasses with Ca3Ga2Ge3O12:Nd composition, containing 0.2 and 1.0 wt% of the Nd2O3 were presented and analysed. The oscillator strengths and phenomenological intensity parameters Ωt (Ω2, Ω4, and Ω6) were obtained using standard Judd-Ofelt theory. Calculated Ωt parameters, radiative transitions rates, branching ratios and radiative lifetime for Nd3+ centres in the glass with Ca3Ga2Ge3O12 composition were analysed and compared with corresponding Nd3+ parameters in their crystalline analogue with garnet structure. Experimental lifetimes are compared with those calculated, and quantum efficiency of Nd3+ centres from 4F3/2 emitting level in the glass with Ca3Ga2Ge3O12 composition is estimated. Incorporation peculiarities and local structure of Nd3+ luminescence centres in the glass with Ca3Ga2Ge3O12 composition and corresponding Ca3Ga2Ge3O12:Nd3+ garnet laser crystals are considered. On the basis of extended X-ray absorption fine structure (EXAFS) spectra (L3-edge) of rare-earth elements analysis it has been shown that Nd3+ luminescence centres in the CaO-Ga2O3-GeO2 glass network occupy structural sites with the coordination number to oxygen N = 6. [ABSTRACT FROM AUTHOR]

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]

Optical absorption spectra and luminescence spectra were recorded as a function of temperature between 295 K and 800 K for single crystal samples of Gd2SiO5:Dy3+, Lu2SiO5:Dy3+, LiNbO3:Dy3+, and Gd3Ga3Al2O12:Dy3+ fabricated by the Czochralski method and of YAl3(BO3)4:Dy3+ fabricated by the top-seeded high temperature solution method. A thermally induced change of fluorescence intensity ratio (FIR) between the 4I15/2→ 6H15/2 and 4F9/2 → 6H15/2 emission bands of Dy3+ was inferred from experimental data. It was found that relative thermal sensitivities SR at 350 K are higher for YAl3(BO3)4:Dy3+ and Lu2SiO5:Dy3+than those for the remaining systems studied. Based on detailed examination of the structural peculiarities of the crystals it was ascertained that the observed difference between thermosensitive features cannot be attributed directly to the dissimilarity of structural factors consisting of the geometry and symmetry of Dy3+ sites, the number of non-equivalent Dy3+ sites, and the host anisotropy. Instead, it was found that a meaningful correlation between relative thermal sensitivity SR and rates of radiative transitions of Dy3+ inferred from the Judd–Ofelt treatment exists. It was concluded that generalization based on the Judd–Ofelt parameters and luminescence branching ratio analysis may be useful during a preliminary assessment of thermosensitive properties of new phosphor materials. [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]

Crystals of LiNbO3 single-doped with Sm3+, Tb3+, or Dy3+ and crystal of LiTaO3 single-doped with Tb3+ were grown by the Czochralski method. Luminescence spectra and decay curves for LiNbO3 samples containing Sm3+ or Dy3+ ions were recorded at different temperatures between 295 and 775 K, whereas those for samples containing Tb3+ ions were recorded at different temperatures between 10 and 300 K. Optical absorption spectra at different temperatures were recorded within the UV-blue region relevant to optical pumping of the samples. It was found that the effect of temperature on experimental luminescence lifetimes consists of the initial temperature-independent stage followed by a steep decrease with the onset at about 700, 600, and 150 K for Sm3+, Dy3+, and Tb3+ ions, respectively. Additionally, comparison of temperature impact on luminescence properties of LiNbO3:Tb3+ and LiTaO3:Tb3+ crystals has been adequately described. Experimental results were interpreted in terms of temperature-dependent charge transfer (CT) transitions within the modified Temperature—Dependent Charge Transfer phenomenological model (TDCT). Disparity of the onset temperatures and their sequence were explained based on the location of familiar zigzag curves connecting the ground state levels of rare earth ions with respect to the band-gap of the host. It was concluded also that LiNbO3:Sm3+ is suitable as an optical sensor within the 500–750 K temperature region whereas LiNbO3:Dy3+ offers the highest sensitivity at lower temperatures between 300 and 400 K. [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 The thermal and optical properties of oxyfluorotellurite (65-x)TeO 2 -20ZnF 2 -12PbO-3Nb 2 O 5 -xSm 2 O 3 (x = 0.5, 2 and 5) glass systems were investigated. Glass thermal stability were monitored by differential thermal analysis (DTA) and adequate thermal stability criteria ΔT, H' and S were determined. It was shown that the thermal stability of the investigated materials increases with the increasing of samarium ions content. The absorption and emission spectra of Sm3+ ions in oxyfluorotellurite glass were recorded in the wide spectral range from UV to NIR. Based on the Judd-Ofelt (J–O) procedure oscillator strengths, phenomenological Judd-Ofelt intensity parameters Ω 2,4,6, radiative transition probabilities, branching ratios and radiative lifetimes of luminescent levels were determined. The luminescence decay curves of the 4G 5/2 (Sm3+) excited state were recorded for three different concentrations of Sm3+ and corresponding experimental lifetimes were determined. Photoluminescence emission spectra were measured in the temperature range from 300 K up to 725 K to evaluate the materials under study as luminescent temperature sensor. Highlights • (65-x)TeO2-20ZnF2-12PbO-3Nb2O5-xSm2O3 (x = 0.5, 2, 5 mol%) glasses were prepared. • Thermal properties of glasses were analyzed as a function the Sm3+ concentrations. • The optical properties of Sm3+ ions in oxyfluorotellurite glass were assessed. • The materials under study were evaluated as luminescent temperature sensors. [ABSTRACT FROM AUTHOR]

Oxyfluorotellurite (65-x)TeO 2 –20ZnF 2 –12PbO–3Nb 2 O 5 –xLn 2 O 3 (Ln = Nd 3+ and Yb 3+ , x = 0.5, 2 and 5) and (65-x-y)TeO 2 –20ZnF 2 –12PbO–3Nb 2 O 5 –xNd 2 O 3 –yYb 2 O 3 (x = 0.5, y = 2 and x = 0.5, y = 5) glass systems were fabricated and their optical and thermal properties were investigated. Absorption and emission spectra of RE admixture ions in oxyfluorotellurite glasses were measured and examined at room temperature in the wide spectral region. Oscillator strengths, phenomenological Judd-Ofelt (J–O) intensity parameters, radiative transition probabilities, branching ratios and radiative lifetimes of luminescent levels were determined. Luminescence decay curves of the 4 F 3/2 (Nd 3+ ) and 2 F 5/2 (Yb 3+ ) excited states were recorded and comprehensively analyzed for the single-doped Nd 3+ and Nd 3+ –Yb 3+ co-doped samples. Relaxation dynamics of luminescent levels were studied as a function of the Nd 3+ and Yb 3+ concentrations. An effective non-resonant phonon assisted energy transfer from neodymium to ytterbium was observed and studied. It was found that good thermal stability combined with proper spectroscopic parameters of examined Nd, Yb-doped oxyfluorotellurite glasses imply the suitability of these materials for the design of NIR-emitting efficient optical devices. Furthermore, the ability of the Nd 3+ ions in oxyfluorotellurite glass host as luminescent temperature sensor was verified. Relative intensity ratios of neodymium transitions originated in 4 F 7/2 / 4 F 3/2 and 4 F 5/2 / 4 F 3/2 thermally coupled closely-located excited states have been adequately determined and studied. [ABSTRACT FROM AUTHOR]

Strontium metaborate (SrB 2 O 4 ) is a suitable material for use as a matrix for luminescent dopant ions. Similarity of ionic radii of strontium and divalent europium makes it an excellent host for Eu dopant. This paper reports on the Czochralski growth and spectroscopic study of SrB 2 O 4 single crystals doped with europium and co-doped with europium and potassium. Based on recorded luminescence spectra it was found that both Eu 3+ and Eu 2+ ions occur in this host. Trivalent europium ions give rise to a narrow-band long-lived red luminescence that is not affected by incorporation of potassium ions. Divalent europium ions emit a UV–blue luminescence, consisting of a large spectral band centered at ca 430 nm. In the absence of potassium ions the decay of this luminescence deviates slightly from a single exponential time dependence with a mean lifetime value of 2.0 ns. In potassium-co-doped sample a strong deviation from a single exponential decay was observed for longer stages of decay, beginning at ca 2.5 ns. This phenomenon was attributed to dissimilarity of relaxation rates of a fraction of europium ions distributed in different lattice sites that are distorted by the presence of big potassium ions. By co-doping the host with alkali ions one can influence the oxidation state of europium ions thereby enhancing the emission of trivalent europium ions. It was concluded that the material under study is a promising phosphor for visible light emission applications. [ABSTRACT FROM AUTHOR]

Highlights: [•] Samarium doped langatate crystal was grown by Czochralski method. [•] Thermal dependences of Sm3+ emission and absorption have been measured. [•] Judd–Ofelt analysis was carried out and radiative transition rates were calculated. [•] Inhomogeneous broadening of spectral lines has been observed. [ABSTRACT FROM AUTHOR]

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]

The 50GeO2-(50-x-y)PbO-yPbF2-xLnF3 glass single doped with Pr3+ and Tb3+ ions was studied. The composition of the material was modified by varying the content of both PbF2 (y = 5, 10, 15 mol%) and LnF3 (x = 0.2 and 2 mol%). The differential thermal analysis (DTA) of as-melted samples was used to determine thermal characteristics. Optical techniques and kinetics measurements were used to monitor the effect of thermal treatment on spectroscopic properties and dynamics of luminescent states of optically-active ions in amorphous and two-phase systems. It was found that non-exponential decays of praseodymium luminescence in as-melted material become exponential or nearly exponential with corresponding longer lifetimes in thermally-treated samples. This effect was not so strong in the Tb3+-doped glass. The influence of the PbF2 content on luminescence dynamics was studied for samples doped with 2 mol% of Pr3+. It was observed that the increase of PbF2 content leads to lengthening of luminescence lifetime, e.g., the 1D2 lifetime increases from 4.1 to 45 µs in 5 and 15 mol% of PbF2 as-melted samples, respectively. [ABSTRACT FROM AUTHOR]

Abstract: The positions of 4f–5d levels of cerium in K5Li2LaF10 crystals were determined to be situated at: 33145cm−1 (zero phonon line), 43700, 45900, 47250 and 54500cm−1. Thermoluminescence glow curves, depend on concentration of Ce3+ and reveals occurrence of several traps with depths ranging from 0.3–0.84eV; the low value of ratio TL/(TL+ssRL) for K5Li2CeF10 (0.07) suggests that the trapping process is almost negligible in contrast to the K5Li2La0.99Ce0.03F10 (0.44) one, where nearly half of the excitation energy is stored in traps. [Copyright &y& Elsevier]

Terbium ions in Gd 3 Ga 3 Al 2 O 12 (GGAG) single crystal exhibit strong luminescence originated in the 5D 3 and 5D 4 multiplets. The decay time of the 5D 3 state is 1072 μs and 724 μs at 5 K and 300 K, respectively. The time dependence of luminescence originated from the 5D 4 multiplet is consistent with single exponential decay, with lifetime values 3579 μs at low temperature and 2902 μs at 300 K. The non-exponential decay curves have been fitted in the frame of Inokuti-Hirayama model, indicating that the dipole-dipole interaction plays an important role in the fluorescence quenching of the 5D 3 level. The calculated R 0 parameter values are equal to 11.56 Å and 12.86 Å for 5 and K 300 K, respectively. The positions of multiplets up to 40000 cm−1 are determined employing the f-shell empirical programs. CIE 1931 coordinates are x = 0.298 , y = 0.664 (green) at 5 K and x = 0.360, y = 0.538 (yellowish green) at 300 K. • A new material has been obtained in the form of single crystal. • A starting stoichiometry is given to minimize segregation process. • Low temperature positions of 4f and 5d states have been determined. • Energy transfer processes have been examined. • Influence of temperature on the Tb transition ratio has been investigated. [ABSTRACT FROM AUTHOR]

Abstract Spectroscopic properties of Gd 3 Ga 3 Al 2 O 12 (GGAG) single crystals co-doped with various configurations of (Eu + Tb); (Eu + Ce); (Tb + Ce) and (Eu+ Tb + Ce) ions have been investigated. The effect of distinct Ln3+ co-doping variations on luminescence of garnet crystals was studied using the different excitation wavelengths. The Ln3+-Ln3+ and host-Ln3+ interplays have been considered in doubly and triply doped GGAG:Ln3+. The crystals containing cerium ions are characterized by mainly broadband emission in the 450–750 nm spectral region that is adequately modified in green and red spectral range in the samples co-doped with terbium and europium, respectively. The Eu3+ luminescence in materials under study is selectively excited employing solely f-f europium transitions. Contrary to that, emission of terbium and cerium occur as result of interaction with Gd3+ and adjacent co-dopants. Graphical abstract Image 1 Highlights • Novel doubly and triply - doped GGAG garnet crystals for lighting system applications. • Luminescent and excitation properties of GGAG:Ce,Tb,Eu crystals. • Optimization of phosphor color by various combination of Ce, Tb, Eu dopants. • Evaluation of Ln3+-Ln3+ and host-ion interactions. [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]

Single crystals of Gd 3 Al 2.5 Ga 2.5 O 12 (GAGG) doped with Tm 3+ ions and co-doped with Ho 3+ and Tm 3+ ions were grown by the Czochralski technique and investigated employing methods of optical spectroscopy. The room temperature absorption spectra of GAGG:Tm 3+ were analysed in the framework of the Judd-Ofelt theory. Obtained phenomenological parameters Ω 2 = 0.62 × 10 −20 cm 2 , Ω 4 = 1.41 × 10 −20 cm 2 and Ω 6 = 0.80 × 10 −20 cm 2 were used to determine rates of radiative transitions, branching ratio values and radiative lifetimes for excited multiples of incorporated Tm 3+ ions. Effect of Tm 3+ concentration on decay curves of Tm 3+ luminescence was examined and spectroscopic parameters characterizing the donor-acceptor interaction responsible for self-quenching of the emission from the 1 D 2 , 1 G 4 and 3 H 4 multiplets were evaluated applying the Inokuti-Hirayama model. The crystal field splitting of Tm 3+ multiplets were determined based on low temperature absorption and emission spectra. The emission cross section for Tm 3+ : 3 F 4 → 3 H 6 luminescence was determined to be 0.31 × 10 −20 cm 2 at maximum and corresponding experimental lifetime amounts to 4.3 ms resulting in quantum efficiency η = 0.79. The calculated ratio of Tm-Ho to back-transfer processes (C Tm-Ho /C Ho-Tm ) is 5.18. [ABSTRACT FROM AUTHOR]

Spectroscopic features and laser performance of a novel thulium-doped scandium yttrium silicate crystal Tm 3+ :ScYSiO 5 (Tm:SYSO) are presented. The experimental lifetime of luminescence related to the 3 F 4 – 3 H 6 laser transition of Tm 3+ amounts to 1.1 ms, which is smaller by a factor of three than the calculated radiative lifetime value due to the contribution of nonradiative relaxation. As a consequence of the internal disordered structure of the SYSO host crystal, the luminescence bands of 3 F 4 – 3 H 6 and 3 H 4 - 3 H 6 show significant inhomogeneous spectral broadening as compared with that of SSO. The laser performances were evaluated in an end-pumped cavity using a CW semiconductor laser as a pump source. In a free run regime, the Tm:SYSO laser delivered a maximum output power of 580 mW at 2022 nm, corresponding to a slope efficiency of 17.4%. With a birefringent quartz plate inserted into laser cavity, the laser output wavelength was continuously tuned from 1950 nm to 2057 nm and dual wavelength operations at 2011 nm and 2020 nm, 1987 nm and 2045 nm, 2022 nm and 2044 nm were observed. [ABSTRACT FROM AUTHOR]

Oxyfluoride glasses doped with erbium and ytterbium have been fabricated at T = 1460 °C. To prepare glass-ceramic systems, the precursor glasses were annealed at temperature 750 °C for 2 h. The ordered fluoride-like crystalline phases were recognized applying XRD, SAED and EDS methods. The spectroscopic properties of the glass-ceramic samples were significantly different as compared to those observed in the precursor glass. Particularly, the emission spectra of glass-ceramics are evidence that some of Er 3 + and Yb 3 + ions reside into the ordered environment. Up-conversion phenomena attributed to visible anti-stokes emission of Er 3 + has been observed under excitation of Yb 3 + ions by a 980 nm diode laser. Especially, the substantial enhancement of red up-converted luminescence was observed in the glass-ceramic system. Dissimilar spectral characteristic and relation of both aforementioned emissions examined in glass and glass-ceramic samples point at different contributions of processes relevant to up-conversion phenomena. The detailed analysis of the crucial Er 3 + and Yb 3 + excited states relaxation dynamics and their spectroscopic qualities has been performed to determine the mechanisms which lead to conversion of the infrared excitation into visible emission. [ABSTRACT FROM AUTHOR]

Mixed garnet crystals with nominal stoichiometry Gd 3 Al 2.5 Ga 2.5 O 12 undoped, single doped with Sm 3+ , Ho 3+ , Er 3+ and Yb 3+ and co-doped with Ho 3+ + Yb 3+ and Er 3+ + Yb 3+ were grown by the Czochralski method. Optical spectra and thermal conductivity of obtained single crystal samples were measured and analyzed. Recorded optical absorption spectra revealed that the intensity and spectral characteristics of color centre absorption in the UV region, close to the UV absorption edge of the host, are affected by the type of incorporated rare earth ions. On the other hand, spectral characteristics of stable color centers induced by an intense UV irradiation of crystals depend weakly on the rare earth admixture. Low temperature optical spectra provided the evidence that Sm 3+ ions and Er 3+ ions occupy at least two different types of sites in this host but Yb 3+ ions seem to be located preferentially in identical sites. Thermal conductivity of the crystals at 300 K, weakly affected by incorporated rare earth ions, is comparable to that reported for ordered gallium gadolinium garnet crystals. At cryogenic temperatures, i.e. below ca 80 K, thermal conductivities of the crystals containing rare earth ions are markedly smaller than that of undoped one, however. [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]

Undoped and samarium-doped SrB 4 O 7 polycrystalline samples were prepared by a solid state reaction method in air. XRD examination revealed that the undoped sample is consistent with the pure SrB 4 O 7 phase but in samarium-doped sample in addition to the main tetraborate SrB 4 O 7 phase there is a little amount of metaborate. Based on preliminary spectroscopic examination it was ascertained that Sm 2+ ions are incorporated without measurable traces of Sm 3+ admixture. High resolution luminescence spectra and decay curves of Sm 2+ luminescence were measured as a function of temperature in the 5–550 K temperature region. Energies of crystal field components of the 7 F J (J = 1–5) multiplets at 5 K and those of the 5 D 1 multiplet at 300 K were determined from luminescence spectra and used subsequently as input data for the crystal field calculation. Performed crystal field calculation predicts the energy level scheme for the 4f 6 configuration of Sm 2+ in SrB 4 O 7 up to 29000 cm −1 and makes it possible to assess the contribution of transitions from the excited states above the 5 D 1 to luminescence phenomena. Evaluated activation energy E a ∼4600 cm −1 characterizing a steep decrease of the 5 D 0 lifetime of Sm 2+ between 320 K and 550 K indicates strongly that electronic origin of the lowest energy 7 F 0 – 4f 5 d 1 vibronic transitions is located around 19200 cm −1 , slightly below the 7 F 0 – 5 D 3 transition energy. [ABSTRACT FROM AUTHOR]

We have investigated the thermal and spectroscopic properties of Pr 3+ -doped new tellurite matrix with the molar composition 60%TeO 2 –27%WO 3 –10%PbO–3%Lu 2 O 3 (TWPLu). The differential thermal analysis has shown that addition of Lu 2 O 3 to the glass results in an increasing resistance against crystallization. The ellipsometric data have provided a Sellmeier-type dispersion relations of the refractive index of the investigated glasses. The optical absorption edge of the TWPLu matrix has been described within the Urbach approach, while the absorption and fluorescence spectra of the Pr 3+ -doped TWPLu glasses have been analyzed in terms of the standard Judd–Ofelt theory along with the luminescence decay of the 3 P 0 and 1 D 2 levels of the Pr 3+ ion. A significant influence of the Pr 3+ ion concentration on the photoluminescence intensity as well as on decrease of the lifetimes of both levels has been explained by a non-radiative energy transfer between the ions through cross-relaxation and energy migration processes. [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]

Abstract: Lead borate glasses were prepared and then heat treated in order to obtain transparent glass-ceramics. Controlled crystallization of precursor lead borate glass at appropriate annealing temperature and time led to formation of the PbWO4 crystallites. The observed broad blue emission band is related to the PbWO4 crystallites. The influence of PbX2 content (X=F, Cl, Br), PbF2 concentration and lanthanide doping (Eu, Dy) on the excitation and emission spectra of lead borate glass-ceramics containing PbWO4 phase was examined. The relationship between Pb–X bond and spectral line width of the blue emission can be successfully observed, when halogen X ions (X=F, Cl or Br) are also present in the distorted PbWO4 crystallites. [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: Er3+-doped KCaY(VO4)2 microcrystalline samples were synthesized using a high temperature solid-state reaction technique. Spectroscopic properties of Er3+: KCaY(VO4)2 are studied and the nature of emissions is discussed. A strong green and infrared luminescence were observed under excitation at 314nm in the O2−→V5+ charge-transfer transitions and direct excitation of Er3+ ions at 435nm. A strong emission lines in the blue region are due to the transitions of VO4 3− ions have been observed at 77K. The Judd–Ofelt parametrization scheme has been applied to the analysis of the room temperature absorption spectra in order to evaluate the intensity parameters, the branching ratios and the radiative lifetimes of the 4I13/2, 4I11/2, 4F9/2 and 4S3/2 emitting levels. The effective cross-section has been calculated for the 4I13/2→4I15/2 transition, indicating that the title compounds is a promising active medium for application in the three-level laser system. The up-conversion emission in Er3+: KCaY(VO4)2 was investigated at 300K. The decay profiles of the Stokes and anti-Stokes emissions were measured and the mechanism of up-conversion luminescence is discussed. [Copyright &y& Elsevier]

Abstract: The paper presents the synthesis and spectroscopic properties of 46PbO:53P2O5:Ln2O3 glasses, where Ln=Sm or 0.1Sm+0.9Gd. The glasses show intense luminescence dominated by the orange 4G5/2 → 6H7/2 transition. The luminescence branching ratios and quantum yields have been computed using the Judd–Ofelt analysis of relevant absorption spectra and the observed luminescence lifetimes; the maximum found quantum yield was 69%. The lifetimes and the quantum yields depended on the time of heating the samples at high temperature and on the samarium concentration. [Copyright &y& Elsevier]

Abstract: Good optical quality U3+-doped PbCl2 single crystals of the composition Pb0.99U0.01Cl2 have been obtained by the Bridgman–Stockbarger method. Luminescence spectra of the crystals were recorded in a wide spectral range at room and liquid nitrogen temperatures, and are discussed. Strong infrared emission was observed under 514nm laser pumping to the 5f26d1 bands. The lifetimes of the emitting levels in the visible and near infrared region are given. [Copyright &y& Elsevier]

Abstract: The luminescence hosts K3YF6 and K3GdF6 were obtained in a single-crystal form. Their crystal structure was determined from single-crystal X-ray diffraction data. Both crystals adopt monoclinic system with space group P21/n, . Lattice parameters for K3YF6 are refined to the following values , , , and for K3GdF6 , , , . The vibrational analysis, IR and Raman spectroscopy at room temperature, was applied to these compounds in order to study the site symmetry of Y3+ and Gd3+ ions. [Copyright &y& Elsevier]

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: Upon UV–VUV excitation terbium doped K5Li2LaF10 emits white light coming from the 5D3 and 5D4 multiplets for content of Tb3+ up to 10at%. For higher concentrations (80 and 100at%) the emission becomes green. In excitation spectrum, recorded at 12K, the positions of the zero-phonon lines are not well determined. The spin allowed f–d transitions in this spectrum are similar to the cerium one in K5Li2LaF10: Ce3+, as van Pieterson proposed in the frames of Dorenbos’ model. The maxima of these terbium f–d transitions are found at: 46,976, 57,124, 59,404, 60,629 and 67,110cm−1. The lowest forbidden, high-spin d band is situated at 39,193cm−1. The lifetime of the 5D4 multiplet is 7.5ms and does not depend on the terbium concentration, but the 5D3 lifetimes are strongly influenced and amount to: 2710, 2130, 14.1, 9.5μs for 2, 10, 80, 100at% of terbium, respectively. This is in agreement with the colour rendering of these samples. [Copyright &y& Elsevier]

Spectra and decay curves of luminescence induced in a single crystal of LiTaO 3 :Pr3+ by femtosecond light pulses at different wavelengths from the UV-Blue and NIR regions were recorded and analyzed. It was found that excited levels involved in the broad UV absorption band of LiTaO 3 : Pr3+ are not able to relax via radiative transitions but they feed nonradiatively excited states of the ground Pr3+ configuration. Femtosecond pulse excitation in the NIR region results in an up-converted visible luminescence weakly affected by the pulse wavelength within the 1200 nm–1800 nm region. Spectra acquired imply that the supercontinuum (SC) generated does not promote single - or double-photon processes that may feed the 3P 0 or 1D 2 levels via transitions within the ground 4f2 configuration. It was concluded that the excitation mechanism is consistent with the multiphoton excitation (MPE) that feeds the 5d levels of Pr3+. • Conversion of femtosecond pulses into optically uniaxial system. • Down and up-conversion phenomena in LiTaO 3 :Pr3+ crystal. • Effect of supercontinuum generation on Pr3+ excited states excitation. • Ultrashort pulses induced change of electrical conductivity. [ABSTRACT FROM AUTHOR]

Single crystal of La 3 Ga 5.5 Ta 0.5 O 14 (LGT) doped with Dy3+ was fabricated by the Czochralski technique and investigated employing methods of optical spectroscopy. Polarized optical absorption spectra and luminescence spectra were recorded at room temperature. Unpolarized absorption and luminescence spectra were recorded at 10 K. Spectra of blue luminescence related to transitions 4I 15/2 , 4F 9/2 → 6H 15/2 were recorded at several temperatures in the 300–773 K region. Dy3+ ions have the same symmetry sites in LGT but their spectra show inhomogeneous broadening due to structural disorder of the host and are markedly anisotropic. Results of the Judd-Ofelt treatment made it possible to assess emission cross sections for the 4F 9/2 → 6H 15/2 blue luminescence and for the 4F 9/2 → 6H 13/2 yellow luminescence employing Fuchtbauer-Ladenburg formula and reciprocity method. In particular, a spectral distribution of La 3 Ga 5.5 Ta 0.5 O 14 : Dy3+ σ-polarized luminescence band with an emission cross section σ em = 0.51 × 10−20 cm2 at 573.5 nm is favorable for a laser operation in the visible. Interpretation of the effect of temperature on the blue emission spectra leads to the conclusion that La 3 Ga 5.5 Ta 0.5 O 14 : Dy3+ is promising for application as luminescent thermometer. • Novel single crystal La 3 Ga 5.5 Ta 0.5 O 14 :Dy (LGT:Dy). • Detailed analysis of optical spectra and luminescence decay curves. • Potential visible laser operation at 573.5 nm. • Temperature sensitivity of LGT:Dy luminescence. [ABSTRACT FROM AUTHOR]

In this work, spectroscopic properties of (Lu 0.25 Gd 0.75) 2(1-x) Tm 2x SiO 5 (x = 0.04 and 0.005) single crystals were investigated. The material was found to be biaxial, exhibiting strong optical anisotropy, as clearly demonstrated in polarized absorption and emission spectra. Data from room temperature polarized absorption spectra were used in calculations within the phenomenological Judd-Ofelt model. The intensity parameters Ω t were established at Ω 2 = 3.24 (±0.58), Ω 4 = 2.96 (±0.24) and Ω 6 = 0.86 (±0.14) [10−20 cm2]. The values of fluorescence lifetimes of the 1D 2 and 1G 4 levels were measured and subsequently compared with those calculated using the Judd-Ofelt theory. The strong absorption bands located at wavelengths around 355, 460 and 790 nm, related to the 3H 6 → 1D 2 , 1G 4 , 3H 4 transitions, were found suitable for optical pumping of the investigated material. The characteristics of emission spectra recorded in the blue (ca. 455 nm) and IR (ca. 1750 nm) regions indicate that further investigations of stimulated emission within those wavelength ranges are well justified and can be considered promising. • Spectroscopic investigations of Tm doped (Lu 0.25 Gd 0.75) 2 SiO 5 single crystals were conducted. • Material shows high potential for lasing in IR region ca. 1900 nm. • Influence of Anisotropy and temperature on spectroscopic properties is reported. [ABSTRACT FROM AUTHOR]