Spectral properties and energy transfer of Tm^3＋/Ho^3＋-codoped Ga2O3-Bi2O3-GeO2-PbO glasses

The 2.0 μm emission originating from Ho^3＋：^5I7→^5I8 were investigated upon excitation with 808 nm laser diode （LD） transition in Ho^3＋/Tm^3＋-codoped gallate-bismuth-germanium-lead glasses Energy transfer （ET） process between Tm^3＋： ^3F4 level and Ho^3＋： ^5I7 level was also discussed. It was noted that the measured peak wavelength and stimulated emission cross-section of Ho^3＋-doped bismuth-germanium-lead glasses were -2.02 μm and 5.1×10^-21 cm^2, respectively. Intense emission of Ho^3＋ in Tm^3＋/Ho^3＋-codoped GBPG glass were observed, which resulted from the ET between Tm^3＋： ^3F4 and Ho^3＋： ^5I7 level upon excitation with 808 nm LD.     

Preparation and Luminescence of Er^3＋ Doped Oxyfluoride Glass Ceramics Containing LaF3 Nanocrystals

Er^3＋ doped transparent oxyfluoride glass ceramics version and near infrared luminescence behavior of Er^3＋ in containing LaF3 nanocrystals were prepared and the up-conglasses heat-treating time and temperature, the size （varied from 0 to 19 and glass ceramics were investigated. With increasing nm） and crystallinity （varied from 0 to 47%） of LaF3 nanocrystals in the glass ceramics are increased. The up-conversion luminescence intensity of Er^3＋ ions in the glass ceramics is much stronger than that in the glasses The near infrared emission of Er^3＋ ions in and increased significantly with increasing heat-treating time and temperature the glass ceramics is found to be similar to that in the glasses.     

Synthesis and optical properties of Dy~（3＋）, Li~＋ doped CaMoO_4 phosphor

A series of CaMoO4 phosphors doped with trivalent dysprosium ions (Dy3+) and lithium (Li+) were prepared by solid state method at 750 °C for 3 h. X-ray diffraction (XRD) confirmed the crystal structure and quality of phosphors. Scanning electron microscopy (SEM) in- dicated that the phosphors presented good crystalline state, and the crystalline grain sizes were about 0.5-3.0 μm. The emission spectra showed that the phosphors had intense emission at 480 (4F9/2→6H15/2), 576 (4F9/2→6H13/2) and 660 nm (4F9/2→6...     

Spectroscopic investigations of Gd3Sc2Ga3O12 garnet doped with Cr^3＋ and Nd^3＋ ions

Absorption, excitation and emission spectra as well as decay time measurements at 10, 77, and 300 K were performed for Ga₃Gd₃Sc₂O₁₂ garnet single-crystal doped with Cr³⁺ and Nd³⁺ ions. Strong reabsorption of Cr³⁺ emission by Nd³⁺ absorption lines was observed. The assignments of f–f and d–d transitions were proposed. The broad emission band of chromium ions is an indication that weak/intermediate crystal field strength is present at the Cr³⁺ site.     

Effect of Y3＋, Gd 3＋and La3＋dopant ions on structural,optical and electrical properties of o-mullite nanoparticles

Dielectric ceramics of M(x) Al6(1–x) Si2 O13 doped mullite were synthesized via co-precipitation technique. The X-ray diffraction profiles revealed that these nanoparticles were crystallized well and the volume of mullite unit cell was increased as a function of the ionic radius of dopant ion. TEM images showed regular orthorhombic crystal morphology for the pure mullite sample. Meanwhile, the doped samples exhibited slightly distorted crystal morphology of larger particle sizes. DSC thermograms evinced that the exothermic peak temperature of mullite was shifted to the lower value with M3+ion insertion. The photoluminescence spectra were studied for mullite samples, and it was found that the intensity of the emission spectra was affected by the M3+ion type. It was found that, Y3+doped mullite achieved the minimum dielectric loss value of 0.01 in the radio wave frequency region(1 MHz). Meanwhile, Gd3+ doped mullite achieved the minimum dielectric loss value of 0.09 in the microwave frequency region(1 GHz).     

Spectroscopic Properties and Judd-Ofelt Theory Analysis of Er^3＋-Doped Heavy Metal Oxyfluoride Silicate Glass

Er^3 -doped heavy metal oxyfluoride silicate glass was fabricated and characterized, and the absorption spectrum and fluorescence spectrum of the glass were studied. The Judd-Ofelt intensity parameters Ωt(t=2, 4, 6), spontaneous transition probability, fluorescence branching ratio and radiative lifetime of each energy levels for Er^3 were calculated by Judd-Ofelt theory, and stimulated emission cross-section of ^4I13/2→^4I15/2 transition was calculated by McCumber theory. The results show that fluorescence full width at half maximum and stimulated emission cross-section of Er^3 -doped heavy metal oxyfluoride silicate glass are broad and large, respectively. Compared with other host glasses, the gain bandwidth property of Er^3 -doped heavy metal oxyfluoride silicate glass is close to those of tellurite and bismuth glasses, and has advantage over those of silicate, phosphate and germante glasses.     

Study on the green upconversion saturation in Er^3＋ doped oxyfluoride teilurite glass

The upconversion emission spectra of Er³⁺ doped oxyfluoride tellurite glasses excited by 808 nm laser diode (LD) were measured. The dependence of 550 nm upconversion emission on the excitation intensity was analyzed. Quadratic intensity dependence was only observed at weak excitation intensity. With increasing the excitation intensity, saturation was turned out. The experimental results were fitted to a model based on the rate equations.     

Luminescence properties of YAl3（BO3）4 phosphors doped with Eu^3＋ ions

YAl3 （BO3）4： Eu^3＋ phosphors were prepared by the conventional solid state reaction. The phase structure and morphology were investigated by X-ray diffraction （XRD） and scanning electron microscope （SEM）. Doping YAl3（BO3）4： Eu^3＋ phosphors with concentration of Eu^3＋ ions of 0, 2, 5, 8 and 10 mol% were studied and their luminescent properties at room temperature were discussed. The excitation spectrum of Y0.95Eu0.05Al3（BO3）4 was composed of a broad band centered at about 252 nm and a group of lines in the longer wavelength region. In the emission spectra, the peak wavelength was about 614 nm under a 252 nm UV excitation. The optimal doping concentration of Eu^3＋ ions in YAl3（BO3）4： Eu^3＋ phosphors was 8 mol%.     

Energy transfer processes from Yb3＋ to Ln3＋ （Ln=Er or Tm） in heavy metal glasses

Heavy metal glasses doubly doped with Yb3+ and Ln3+ ions(Ln=Er or Tm) were studied. Glass host matrices were limited to lead borate glass and lead germanate glass. Efficient resonant(Yb3+-Er3+) and non-resonant(Yb3+-Tm3+) energy transfer was observed for the studied systems. Near-infrared luminescence spectra at 1.53 μm(Er3+) and 1.9 μm(Tm3+) were detected under excitation of Yb3+ by 975 nm diode laser line. They corresponded to 4I13/2→4I15/2(Er3+) and 3F4→3H6(Tm3+) transitions of rare earth ions, respectively. The unusual large spectral linewidth nearly close to 110 nm for 4I13/2→4I15/2 transition of Er3+ ions in lead borate glass was obtained, whereas long-lived near-infrared luminescence at 1.53 μm was detected in lead germanate glass. Quite different situation was observed for Yb3+-Tm3+ doubly doped glasses. In contrast to lead borate glass, near-infrared(3F4→3H6) luminescence spectra were registered for Tm3+ ions in lead germanate glasses, only. These phenomena strongly depended on stretching vibrations of glass host, which was confirmed by FT-IR spectroscopy.     

Luminescence properties of Tm^3＋/Yb^3＋, Er^3＋/Yb^3＋ and Ho^3＋/Yb^3＋ activated calcium tungstate

CaWO4 phosphor activated by the Tm3+/Yb3+,Er3+/Yb3+ and Ho3+/Yb3+ ions were synthesized by a traditional high-temperature solid-state method.The crystal structures and morphologies of the products were characterized by X-ray powders diffraction method(XRD) ,infrared spectra(FT-IR) and scanning electron microscopy(SEM) .The samples were found to show up-conversion luminescence properties.CaWO4 doped with Tm3+/Yb3+ showed blue luminescence characteristic of Tm(III) ion in the range of 460-485 nm,corresponding to the 1G4→3H6 electronic transition.CaWO4 doped with Er3+/Yb3+ showed strong green luminescence at 510-565 nm(2H11/2,4S3/2→4I15/2) and weak red luminescence at 640-685 nm(4F9/2→4I15/2) of Er(III) ion.CaWO4 doped with Ho3+/Yb3+ phosphor emitted green luminescence at 525-560 nm(5S2,5F4→5I8) and red luminescence at 630-670 nm(5F5→5I8) and at 730-770 nm(5S2,5F4→5I7) ,which is the characteristic of Ho(III) ion.     

A study on fluorescence properties of Eu3+ ions in alkali lead tellurofluoroborate glasses

Glasses with chemical composition of (in mol.%): 26 RF-20 PbO-10 TeO2-43 H3BO3-1 EuO3 (RLTB) were prepared by conventional melt quenching method. The Judd-Ofelt intensity parameters Ω2 and Ω6 were obtained from the absorption intensities of 7F0→5D2 and 7F0→5L6 transitions, respectively. In order to overcome the problem of applicability of Judd-Ofelt analysis at room temperature due to the overlapping of the transitions originating from 7F0 and 7F1 levels of Eu3+ ion, the effect of the thermalization on the population of energy levels was taken into account. The photoluminescence spectra contained five emission bands originating from the 5D0 metastable state to 7FJ (J=0, 1, 2, 3, 4) lower lying states. The decay profiles were found to be single exponential in all the three glasses. The measured lifetimes (τmes) were in good agreement with the calculated lifetimes (τcal) obtained by using the thermally corrected Judd-Ofelt intensity parameters.     

Up-Conversion Properties of Oxy-Fluoride Glasses Co-Doped with Ho3+ and Yb3+

Oxy-fluoride glasses with composition of 25SiO2-65PbF2-9.4AlF3-0.1HoF3-0.5YbF3 were prepared. Their up-conversion fluorescence characteristics were investigated by 980 nm laser. Two emission peaks were observed at 540 and 650 nm. The up-conversion mechanism and processes were analyzed. The relationship between pumping power and relative intensity of emissions was discussed. From the dependence, it is known that the emissions centered at 540 and 650 nm are both attributed to two-photon process.     

Up-conversion luminescence of Tm3+/Yb3+ co-doped oxy-fluoride glasses

The oxy-fluorosilicate glasses co-doped with Yb3+/Tm3+ were prepared.The absorption spectra were recorded.The Tm3+ ion showed two absorption bands,with one at 774 nm due to 1G4→3H6 transition and the other at 667 nm due to 1G4→3F4 transition.The energy transfer between Tm3+ ion and Yb3+ ion and the up-conversion fluorescence of Tm3+ ion were investigated using 980 nm LD excitation.The results showed that the blue and red emissions were three-photon absorption processes corresponding with 1G4→3H6 and 1G4→3F4...     

Tm3+-doped tellurite glass with Yb3+ energy sensitized for broadband amplifier at 1400-1700 nm bands

A kind of novel experiment was disclosed as it possessed two bands of fluorescence emission at 1.4 and 1.6 μm, which were per-fectly complimentary to the current C band of optic communication. The fluorescence was based on energy transfer and up-conversion proc-esses between Tm3+ and Yb3+ under direct pumping of 975 nm LD. The spectra and lifetimes of Tm3+ fluorescence in the tellurite glass were described. The corresponding fluorescence characteristics and energy migration process were analyzed by the method of lifetime and inten-sity comparison. The mechanism of the up-conversion based IR fluorescence was presented upon analyzing the multi-photon pumping proc-ess. The potential advantages of Tm3+/Yb3+ co-doped tellurite glass as amplifier material were concluded.     

Optical properties of Eu2+-doped strontium borate glasses containing F- and Li+ ions

In this experiment, strontium borate glasses were prepared using the conventional quenching method in air atmosphere. Optical absorption, photoluminescence excitation and emission spectra, X-ray excited luminescence (XEL), and luminescence decay curve of the as-prepared glasses were investigated at room temperature. The as-prepared glasses had two kinds of Eu ions, i.e., Eu2 and Eu3 . Compared with the reported results of strontium borate glasses, Eu2 luminescence was enhanced in the studied strontium borate glasses coprepared with F- and Li ions. The coexisting of Li or F- in the borate glasses could create more negative defect VSr″ and stabilize Eu2 ions, which might act as donor of electrons;For the F- doping, the new center of B(O, F)4 (or BO3F) and BO2F2 units could be considered to be the distorted (BO4), which were needed as a rigid framework to stabilize the divalent rare earth ions.     

Thermal and radiative characteristics of oxyfluoride glass singly doped with lanthanide ions

Rare earths-doped oxyfluoride glasses based on germanium oxide and lead fluoride were prepared from commercial raw materials. The glasses with general composition of 50GeO2-(50-x-y)PbO-yPbF2-xLnF3 (Ln=Pr3+-Yb3+), contained different concentrations of optically active dopants (x=0.2 mol.% and 2 mol.%) and PbF2 (y≤15 mol.%). The differential thermal analysis (DTA) was used to determine both thermal characteristic and thermal stability properties of the glasses in the function of the kind of dopant, its concentration, and a glass composition. Characteristic glass temperatures such as glass transition temperature (Tg), glass crystallization temperature (Tc) and temperature corresponding to the maximum of the crystallization rate (Tpc) were evaluated. On the basis of obtained results, the thermal stabilities of glasses under study were evaluated using various thermal stability criteria (Dietzel factor ?T, Saad-Poulain factors H' and S). It was found that the increase in rare earth fluoride contents influenced thermal characteristics when the characteristic temperatures of the individual glass was shifted towards higher values. The effect of the PbF2 content and the kind of rare earth impurity on the glass stability was observed. Absorption spectra of lanthanide-doped glasses were measured at room temperature and used to determine the phenomenological intensity parameters Ωt and next, to estimate radiative properties of lanthanide ions in this matrix. Radiative transition probabilities of luminescent states of Ln3+, branching ratios and radiative lifetimes were determined. The variation of the Ωt along the lanthanide series was presented and discussed.     

Spectral properties of Tm,Ho:LiYF4 laser crystal

The LiYF4 single crystal codoped with thulium and holmium ions was successfully grown by the Cz method. The optimal technical parameters obtained were as follows: the pulling rate was 0.16 mm/h; the rotation speed was 3 rpm; the cooling rate was 15 °C/h. The result of XRD curve showed that as-grown Tm,Ho:LiYF4 laser crystal belonged to the monoclinic system with scheelite-type structure and space group I41/a. The cell parameters calculated were: a=0.52160 nm, c=1.09841 nm and Z=4. Absorption and fluorescence spectra of Tm,Ho:LiYF4 laser crystal at room temperature were measured and analysed. The absorption cross section, FWHM and absorption coefficient at 779.3 nm calculated were 7.44×10-21 cm2, 8.7 nm and 2.23 cm-1, respectively. An intensive fluorescence emission peak appeared near 2045 nm. The emission cross section and fluorescence lifetime were 0.87×10-20 cm2 and 10.8 ms, respectively. The ratio of Tm-Ho transfer to its back-transfer process was 10.6.     

Influence of CeO2 on scintillating properties of Tb3+-doped silicate glasses

A series of Tb3+-,Ce3+-doped,and Tb3+/Ce3+-codoped silicate glasses were synthesized by melt-quenching technique.Some properties of the investigated glasses were characterized by X-ray photoelectron spectroscopy(XPS),photoluminescence(PL),X-ray excited luminescence(XEL) and thermoluminescence(TL) spectra.The result of XPS revealed that both Ce3+ and Ce4+ ions coexisted in these silicate glasses,and energy transfer from Ce3+ to Tb3+ ions was observed under UV excitation.However,under X-ray excitation the XEL...