Solvothermal fabrication and luminescent properties of Eu2＋/Ce3＋ doped barium lithium fluoride

Phosphors of BaLiF3 doped with Eu or/and Ce were solvothermally prepared at 200°C for 5d and characterized by means of X-ray powder diffraction (XRD) and environment scanning electron microscopy (ESEM). The excitation and emission spectra of the rare earth ions doped BaLiF3 were measured by fluorescence spectroscopy and the effects of Ce3+ ions on the luminescence of Eu2+ ions were investigated. In the codoped Eu2+ and Ce3+ system, the emission intensity of Eu2+ ion gradually increased with the Ce3+ concentration increasing, and the enhancement of Eu2+ fluorescence was due to efficient energy transfer from Ce3+ to Eu2+ in the host.     

Emission of Eu3＋ in sol-gel oxyfluoride glass materials obtained by different preparation methods

Silica glasses doped with Eu3+ ions prepared by sol-gel methods were investigated. The X-ray diffraction(XRD) was used to verify the nature of the studied systems. Excitation and emission spectra of Eu3+ ions in sol-gel glass materials were detected. Red-to-orange luminescence intensity ratios R/O related to integrated intensities of 5D0→7F2 to 5D0→7F1 transitions and luminescence lifetimes for 5D0 state of Eu3+ ions were determined. The results indicated that spectroscopic parameters for Eu3+ ions strongly depended on reagents and their relative ratios used for sol-gel glass preparation.     

Characterization of optical transitions of Eu~（3＋） in lanthanum oxychloride nanophosphor

This paper presented the studies on the optical properties and calculation of spectral parameters of europium doped lanthanum oxychloride nanophosphor for their possible applications in optoelectronic devices. The compound was doped with 0.1 mol% Eu3+ ions. The X-ray diffraction study of prepared sample suggested the tetragonal structure with particle size in the range of 18-21 nm. The photoluminescence (PL) emission spectra showed the bright emission in orange-red region from 580 to 630 nm. The most intense emission peak at 621 nm was due to transition 5D0→7F2 in energy levels of Eu3+ ions. The spectral parameters were calculated from the absorption and emission spectra using Judd-Ofelt intensity parameters. The calculated values of the oscillator strength corresponding to the three transitions 7F1→5D1, 7F1→5D2 and 7F0→5D2 observed at 535, 472 and 465 nm in absorption spectra were 0.30×10-6, 1.36×10-6 and 0.63×10-6, respectively. The value of transi- tion probability (A), stimulated emission cross-section ( ) and radiative lifetime (τrad) corresponding to 621 nm emission peak (transition 5D0→7F2) were 308 s-1, 1.22×10-21 cm2 and 3.24×10-3 s, respectively.     

Luminescence properties of red phosphors Ca_（10）Li（PO_4）_7：Eu~（3＋）

A series of red phosphors Ca10Li (PO4)7:Eu3+ were synthesized by high temperature solid-state reaction method. Their luminescence properties were characterized by means of photoluminescence excitation and emission spectra,CIE chromaticity and quantum efficiency. Results indicated that the phosphors could be effectively excited by the near ultraviolet (NUV) light (393 nm). The main emission peaks of the phosphor were ascribed to the transition 5D0-7F2 (613 and 617 nm) of Eu3+ ion when samples were excited by...     

Role of monovalent co-dopants on the PL emission properties of YAI3（BO3）4：Ce3＋ phosphor

The cerium （Ce3＋） doped yttrium aluminium borate （YAB） phosphor was synthesized by modified solid state reaction. The phosphor＇s phase purity and its emission properties were studied using powder X-ray diffraction pattern and photoluminescence spectroscopy. The synthesized YAB had rhomobohedral crystal structure. The phosphor had two different excitation and emission spectra. By 325 nm excitation, the phosphor had emission at 373 nm and with 363 nm excitation; the phosphor gave violet-blue emission at 418 nm. The UV emission of the phosphor originated due to Ce3＋ ions at the yttrium site and violet-blue emission owing to Ce3＋ ions at non-regular sites viz., A13＋ and interstitial sites. The emission intensity of the phosphor was enhanced when monovalent ions （K＋, Na＋, and F） were added as co-dopants. The crucial role of ionic radii of monovalent co-dopants on the emission enhancement of the YAB：Ce3＋ phosphor was reported. Thermogravimetric study showed that the YAB possessed high thermal stability at up to 900 ℃.     

Synthesis of CaWO4：Eu3＋ phosphor powders via ethylene glycol route and its optical properties

Eu3+ doped CaWO4 with tetragonal system were prepared at comparatively low temperature (125 ?C) in ethylene glycol medium. The phosphor was further investigated by X-ray diffractometer (XRD), photoluminescence spectrophotometer (PL), Fourier transform infra red (FT-IR) spectroscopy and transmission electron microscopy (TEM). XRD analysis indicated a decrease in the unit cell volume of CaWO4 with increasing Eu3+ ion concentration. It indicated the homogeneous substitution of Ca2+ ions in CaWO4 by the Eu3+ ions. TEM images showed that the particle size ranged from 20 to 200 nm and it could extend the application of the nanoparticles. The photoluminescence study showed that the intensity of electric dipole transition (5D0→7F2) at 614 nm dominated over the magnetic dipole transition (5D0→7F1) at 592 nm. The optimum concentration of Eu3+ for the highest luminescence was found to be 20 at.%. The as prepared samples were found to be dis-persible in water and methanol.     

LiZnPO4：Tb^3＋,Ce^3＋ green phosphors with high efficiency

Tb3+ and Ce3+ co-activated LiZnPO4 phosphors with high luminescence efficiency were synthesized by a high temperature solid-state reaction at 1000 oC for 3 h. The XRD patterns, photoluminescence spectra and SEM were recorded and the effects of Tb3+ and Ce3+ concentration, sintering condition on the luminescent properties of as-synthesized phosphors were investigated. The emission spectra under ultraviolet (200-300 nm) radiation showed a dominant peak at 543 nm attributed to the 5D4→7F5 transition of Tb3+, which was greatly en-hanced by the co-doping of Ce3+, indicating that there occurred an efficient non-radiative energy transfer from Ce3+ to Tb3+. The optimal dop-ing concentrations of Tb3+ and Ce3+ were determined to be 9% and 10%, respectively.     

Preparation and luminescent properties of MgTiO3：Eu3＋ phosphor for white LEDs

A novel red phosphor Eu3+ doped magnesium titanate (MgTiO3) was synthesized via sol-gel method. The X-ray diffraction patterns (XRD) revealed that a pure MgTiO3 phase was obtained. Its excitation spectrum consisted of a broad band (<350nm) and a series of narrow bands in the long wavelength, and the strongest excitation peak at 465nm might be exited by GaN-chip to emit red light for white LED. The phosphors showed strong emission at 614nm which could be attributed to the 5D0→7F2 emission of Eu3+ . The emission intensity of MgTiO3:Eu3+ phosphor reached the maximum at the Eu3+ concentration of 3.5mol.%. The luminescent properties (such as emission intensity and decay times) were further improved by introducing Al3+ as a charge compensator, demonstrating potential applications in white LED.     

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.     

Up-conversion luminescence properties of Yb^3＋ and Ho^3＋ co-doped Bi3.84W0.16O6.24 powder synthesized by hydrothermal method

Using polyethylene glycol (PEG) as the surfactant, Bi3.84W0.16O6.24 up-conversion luminescence nano-crystal co-doped with Yb3+ and Ho3+ ions was synthesized by the hydrothermal method. The structure and properties of luminescence powder were studied by X-ray diffraction (XRD) and scanning electron microscope (SEM). It was of cubic system when the sample was synthesized at a low temperature and the particle size was about 30 nm. The results showed that adding surfactants was useful to improve the powder agglomeration and the grain crystal was spherical. The green emission peak at 546 nm and red emission peak at 655 nm, corresponding to the ( 5F4, 5S2)→ 5 I 8 and the 5 F 5 → 5 I 8 transitions of Ho 3+ , respectively, were simultaneously observed at room temperature under excitation of 980 nm semiconductor laser. The up-conversion luminescence intensity was the strongest when the concentration ratio of Yb3+ /Ho3+ was 6:1 and the concentration of Ho 3+ ion was 1.5 mol.%. The up-conversion mechanism was also studied. The green and red emission peaks were the two-photon absorption according to the relationship between the pump power and the luminescence intensity.     

Luminescence properties of a single-host phosphor Bal.8-wSrwLi0.4SiO4： cea＋,Eu2＋,Mn2＋ for WLED

In order to obtain a single-host-white-light phosphor,a series of Ba1.8-w-x-y-zSrwLi0.4-xCexEuyMnzSiO4(BSLS:Ce3+,Eu2+,Mn2+)powder samples were synthesized via high temperature solid-state reaction.The structure and photoluminescence properties were investigated.Under ultraviolet excitation,the emission spectra contained three bands:the 370-470 nm blue band,the 470-570 nm green band and the 570-700 nm red band,which arose from the 5d→4f transitions of Ce3+ and Eu2+,and the 4T1→6A1 transition of Mn2+,respectively.The excitation spectra of the emissions of Ce3+ and Mn2+ ions showed the energy transfer from Ce3+ to Mn2+.White light emission was obtained from the tri-doped samples of appropriate doping concentration under 310-360 nm excitation.     

Electrospinning preparation and luminescence properties of Eu(TTA)3phen/polystyrene composite nanofibers

Efficient luminescent composite nanofibers,composed of polystyrene(PS,Mw=250000) and europium complex Eu(TTA)3phen(TTA=2-thenoyltrifluoroacetone,phen=1,10-phenanthroline) with diameters ranging from 350 nm to 700 nm,were prepared by electrospinning and characterized by scanning electron microscope(SEM),Fourier transform infrared spectroscopy(FT-IR),fluorescence spectroscopy,and thermogravimetric analysis(TG).The room-temperature fluorescence spectra of the composite nanofibers were composed of the typical Eu3+ ion red emission,assigned to the transitions between the first excited state(5D0) and the multiplet(7F0-4).Owing to the incorporation of the europium complex into the PS fiber matrix and the subsequent distortion of the symmetry around the lanthanide ions by the capping PS,the polarization of the Eu3+ ions was enhanced,which increased the probability for electronic dipole allowed transitions.The monochromaticity(5D0→7F2/5D0→7F1) around the Eu3+ ions was also efficiently improved.Judd-Ofelt intensity parameters(Ω2 and Ω4) were determined from the emission spectra based on the 5D0→7F2 and 5D0→7F4 electronic transitions,respectively.The results showed that the Ω2 values of the composite nanofibers were apparently higher than that of the pure complex,indicating an increased covalency degree in the europium first coordination shell due to the modification of PS matrix.The modification of the polymer matrix also resulted in much higher thermal stability of the composite fibers than that of the pure complex.     

Synthesis and characterization of nano-sized YAG:Ce,Sm spherical phosphors

YAG:Ce,Sm spherical phosphors were synthesized by malic acid sol-gel method.The formation process of crystalline was characterized by X-ray diffraction(XRD)technique.The influence of Sm3+ doping on the luminescent intensity and the morphology of phosphors were studied by fluorescence spectrum and scanning electron microscopy(SEM)techniques,respectively.The results indicated that the size of spherical powders was about 100 nm calcined at 1200 ℃ for 3 h.The emission spectra of phosphors showed gradual red-shift from 525 to 540 nm with the increase of doping concentration of Sm3+ ion.A broadband emission spectrum of Ce3+ ion appeared at 540 nm,and a series of emission peaks corresponding to the 4G5/2→6HJ transition of Sm3+ ion also appeared at 617 nm with the doping of Sm3+.The red component of YAG:Ce phosphors increased with the doping of Sm3+.     

Preparation and photoluminescence of Eu-doped oxyfluoride borosilicate glass ceramics

Eu-doped transparent oxyfluoride borosilicate glass ceramics containing Ba2GdF7 nanocrystals were prepared by controlling crys-tallization of melt-quenched glass fabricated under a reductive atmosphere.In the oxyfluoride borosilicate glass ceramics,the mean crystal size of Ba2GdF7 nanocrystals was about 30 nm,which could be observed by X-ray diffraction(XRD) and transmission electron microscopy analysis.The photoluminescence spectra of the samples excited at 392 nm showed that,besides the characteristic sharp emissions of Eu3+ ions,a very intense broadband emission of Eu2+ ions centered at 450 nm appeared.The photoluminescence intensity of Eu3+ and Eu2+ ions in the glass ceramics was much stronger than that in the as-made precursor.The long decay lifetimes of Eu3+ and Eu2+ ions evidenced the partitions of Eu3+ and Eu2+ ions into the Ba2GdF7 nanocrystals.The energy transfer from Gd3+ ions to Eu3+ and Eu2+ ions was confirmed by the excita-tion and emission spectra.     

Synthesis and luminescence properties of BaWO4：Pr^3＋ microcrystal

BaWO4:Pr3+ (hereafter BWO:Pr) microcrystals were prepared via a hydrothermal route, and characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), photoluminescence excitation and emission spectra. The as-prepared products with different morphologies of egg-shape rod, olive-like, and quasi-sphere were obtained by the addition of the surfactants and chelating agents. The emis-sion spectra of BWO:Pr microcrystals showed the strong red emission (642 nm) assigned to the Pr3+ ions of 3P0→3F2 transition with blue ex-citation (484.6 nm, 3H4→3P0).     

Synthesis,structural and optical properties of SrZrO3：Eu3＋phosphor

Eu3+ activated Sr1–xEuxZrO3(x=0.01–0.04) phosphor with perovskite structure was successfully synthesized by using combustion method.The structure,morphology and optical properties of the material were characterized by X-ray diffraction,scanning electron microscopy and fluorescence spectrometry.The XRD results indicated that crystals of SrZrO3:Eu3+ belongs to tetragonal perovskite system.The phosphor could be effectively excited by UV light and the emission spectra results indicated that reddish-orange luminescence of SrZrO3:Eu3+ due to magnetic dipole transition 5D0→7F1 at 593 nm was dominant.Thus,the prepared phosphor showed remarkable luminescent properties which find applications in field emission display(FED) and plasma display panel(PDP) devices.     

Multi-wavelength excitable europium-doped borosilicate glasses for orangered emission：composition-induced structure and valence variation

Europium-doped borosilicate glasses were prepared by melt-quenching procedure in the air.The mixed valence of Eu 2+ and Eu 3+ was identified by photoluminescence spectrum and electron paramagnetic resonance(EPR).The existence of mixed valence was observed owing to the unequivalent substitution and de-polymerization network of the as-prepared borosilicate glasses.The variation of the glass composition in B 2 O 3 /BaO ratios changed the stability of the Eu 3+ ions distinctly.In particular,as-prepared borosilicate glasses exhibited a tri-wavelength light excitable spectra centered at 397,466 and 534 nm to give the broadened orange-red emission at around 592 and 617 nm,due to supersensitive transitions of Eu 3+ ions.This simultaneous tri-wavelength excitation happened to correspond with the emitting wavelength from near ultraviolet,blue AlInGaN chips and that from YAG:Ce 3+.The total quantum yield(QY) of the Eu-doped glasses under 466 nm excitation was evaluated to be 10%,potentially providing a versatile combination with the europium-doped borosilicate glasses for red component addition to improve the quality of white light.     

Luminescent properties of Eu~（3＋） doped Gd_2WO_6 and Gd_2（WO_4）_3 nanophosphors prepared via co-precipitation method

Eu3+ doped Gd2WO6 and Gd2(WO4)3 nanophosphors with different concentrations were prepared via a co-precipitation method. The structure and morphology of the nanocrystal samples were characterized by using X-ray diffraction (XRD) and field emission scanning electron microscopy (FE-SEM), respectively. The emission spectra and excitation spectra of samples were measured. J-O parameters and quantum efficiencies of Eu3+ 5D0 energy level were calculated, and the concentration quenching of Eu3+ luminescence in different matrixes were studied. The results indicated that effective Eu3+:5D0-7F2 red luminescence could be achieved while excited by 395 nm near-UV light and 465 nm blue light in Gd2WO6 host, which was similar to the familiar Gd2(WO4)3:Eu. Therefore, the Gd2WO6:Eu red phosphors might have a potential application for white LED.     

Luminescent properties of red phosphors K2Ba（MoO4）2：Eu3＋ for white light emitting diodes

K2Ba(MoO4)2:Eu3+ phosphors were synthesized by solid-state reaction. The emission and excitation spectra of K2 Ba(MoO4)2:Eu3+ phosphors exhibited that the phosphors could be effectively excited by near ultraviolet (394 nm) and blue (465 nm) light, and emitted red light at 616 nm. The influence of Eu3+concentration, sintering temperature and charge compensators (K+, Na+ or Li+ ) on the emission intensity were investigated. The results indicated that concentration quenching of Eu3+ was not observed within 30mol.% Eu 3+, 600 oC was a suitable sintering temperature for preparation of K2 Ba(MoO4)2:Eu3+phosphors, and K+ ions gave the best improvement to enhance the emission intensity. The CIE chromaticity coordinates of K2 Ba(MoO4)2:0.05Eu3+phosphor were calculated to be (0.68, 0.32), and color purity was 97.4%.     

Luminescence of Er^3＋ in Oxyfluoride Transparent Glass-Ceramics

Erbium doped silicate, germanate, and tellurium-germanate oxyfluoride glasses were prepared in a bulk form. Through appropriate heat treatment of the as-prepared glasses, transparent glass-ceramics (TGCs) were obtained with the formation of β-PbF2∶Er3 nanocrystals in the glass matrix were confirmed by X-ray diffraction. Well-defined diffraction peaks were observed in the samples after heat-treatment. The average crystal diameter of these precipitated crystals from full-width at half-maximum (FWHM) of the diffraction peak was estimated to be between 8 and 13 nm. Optical absorption, photoluminescence, and upconversion luminescence were measured on as-prepared glass and glass-ceramics. Luminescence spectra in the TGC samples revealed well-resolved, sharp stark-splitting peaks, which indicates that a majority of Er3 ions has been incorporated into the crystalline phase of the nanocrystals. The intensity of the visible and near infrared luminescence mostly increases in TSG compared to that in the as-prepared glass. In 1.53 μm absorption and emission bands, the maximum absorption peak is blue-shifted from 1531 to 1507 nm, whereas the maximum emission peak is red-shifted from 1535 to 1543 nm in TGC, as compared with that in glass. The bandwidth at half-maximum (BWHM) of the emission band is significantly broader in TGC than in glass, which is beneficial to the erbium-doped fiber amplifier (EDFA). Upconversion luminescence was measured using 800 nm near-infrared light excitation. Drastically increased upconversion luminescence was observed from the TGC as compared to that from their corresponding as-prepared glasses. In addition to a strong green emission centered at 545 nm because of 4S3/2→4I15/2 transition and a weaker red emission centered at 662 nm because of 4F9/2→4I15/2 transition, generally seen from the Er3 doped glasses, two violet emissions centered at 410 nm because of 2H9/2→4I15/2 transition and centered at 379 nm because of 4G11/2→4I15/2 transition were also observed from the TGC. The increased luminescence was attributed to the decreased effective phonon energy and the increased energy transfer between the excited ions when Er3 ions were incorporated into the precipitated β-PbF2 nanocrystals. The results indicated two attractive spectroscopic properties of the Er3 doped TGC samples, compared to glass samples, namely a reduced multiphonon decay rate and a reduced inhomogeneous broadening. In addition, these oxyfluoride TGC materials were robust, easy and flexibile to process, and possible to be fabricated in the fiber form for device applications.