Magnetooptics of non-Kramers Eu3＋ ions in garnets： analysis complemented by crystal-field splitting modeling calculations

Spectra of absorption, luminescence, magnetic circular dichroism (MCD), and magnetic circular polarization of lumines-cence (MCPL) in Gd3Ga5O12:Eu3+and Eu3Ga5O12 garnets were studied within the visible...     

Energy transfer between Gd^3＋ and Tb^3＋ in phosphate glass

The phosphate glass doped with Gd3+,Tb3+ and Gd3+/Tb3+ were prepared by high temperature melting.The photo-luminescence behavior of Gd3+ and Tb3+ in phosphate glass were investigated by absorption,excitation,and emission spectroscopy.Energy transfer between Gd3+ and Tb3+ in phosphate glass was studied,and it was found that there were two energy transfer mechanisms between Gd3+ and Tb3+ in phosphate glass: one was from 4f7 level of Gd3+ to the 4f8 level of Tb3+,and the other was from 5d level of Tb3+ to 4f7 level of Gd3+.The new findings would be beneficial for the study of Tb3+-doped scintillating phosphate glass.     

Luminescence properties and energy transfer of host sensitized CaMoO4：Tb^3＋ green phosphors

A series of CaMoO 4 :xTb 3+(x=0.01,0.03,0.05,0.07,0.09,0.15 and 0.20) phosphors in pure phase were prepared via high temperature solid-state reaction approach.The crystal structure of the phosphors was investigated by X-ray diffraction(XRD),and the optical properties were investigated by Fourier transform infrared spectroscopy(FT-IR),ultraviolet-visible spectroscopy(UV-Vis) and photoluminescence(PL) spectroscopy.The PL spectra illustrated that these phosphors could be efficiently excited by the charge transfer band of the host and the energy transfer efficiency from the host to the doped activator reached 60% when the doping concentration of the activator Tb 3+ was 20 mol.%.The concentration quenching occurred at x=10 mol.%,from which the critical distance of activator was calculated to be about 1.14 nm.The CIE coordinates were estimated to be close to the standard green value.The host sensitized samples had potential application as green phosphors.     

Preparation and upconversion luminescence of monodisperse Gd2O3：Ho^3＋,Yb^3＋ nanocrystals

Gd2O3:Ho3+,Yb3+ nanocrystals were synthesized via solvothermal method.X-ray diffraction(XRD),transmission electron microscopy(TEM),absorption and upconversion spectra were employed to characterize the synthesized nanocrystals.The results of XRD and TEM showed that obtained Gd2O3:Ho3+,Yb3+ nanocrystals were cubic in crystal structure and uniform spherical in morphology.The average crystallite size was calculated to be 7.5 nm.Green and red up-conversion emissions corresponding to(5F4,5S2)→5I8 and 5F5 → 5I8 transition were observed upon 980 nm excitation at room temperature.The results indicated that both green and red luminescence were based on the two-photon processes.Laser power and doping concentration dependence of the upconverted emissions were studied to understand the upconversion mechanisms.Excited state absorption and energy-transfer processes were discussed as the possible mechanisms for the visible emissions.     

Cooperative energy transfer in Tm3＋and Yb3＋ co-doped phosphate glasses

An efficient near-infrared (NIR) quantum cutting (QC) in Tm3+ and Yb3+ co-doped phosphate glasses was demonstrated, which involved the emission of two NIR photons from an absorbed visible photon via a cooperative energy transfer (CET) from Tm3+ to Yb3+ ions. Judd-Ofelt (J-O) theory was used to calculate the intensity parameters ( 2 , 4 , 6 ), the radiative transition rates (Ar ), and radiative transition lifetime (τ rad ) of Tm3+ . Based on Inokuti-Hirayama’s model, the energy transfer processes were studied and results indicated that the energy transfer of the electric dipole-dipole (Edd) was dominant in this system. Quantum efficiency related to Yb 3+ concentration was calculated, and the maximum QE efficiency reached 169.8%.     

Hydrothermal synthesis and luminescence properties of YW2O6（OH）3：Tb^3＋ green phosphors

YW2O6(OH)3:Tb3+ green phosphors were synthesized at different pH values via a facile hydrothermal method. The structure and optical properties of as-synthesized samples were studied by X-ray diffractometer (XRD), scanning electron microscopy (SEM), photolumi-nescence spectra and luminescence decay curve. The results showed that pure monoclinic YW2O6(OH)3:Tb3+ green phosphors could be ob-tained at pH 2-5. Uniform spherical micro-phosphors of ~5 μm in diameter with narrow size distribution could be prepared at pH 5. pH value had dramatic influence on morphologies, which could be ascribed to the various spatial configurations of different poly-tungstates existing at different pH values. The emission spectra under 261 nm excitation exhibited dominant green emission at 546 nm. The green emission inten-sity reached the maximum value at pH 5 due to the high packing density of the obtained phosphor.     

Efficient near-infrared quantum cutting by Ce~（3＋）-Yb~（3＋） couple in GdBO_3 phosphors

Ce3+ and Yb3+ co-activated GdBO3 phosphors were prepared by a conventional solid-state reaction method. X-ray powder diffraction, photoluminescent spectra and decay curves were used to characterize their structural and luminescent properties. An efficient near-infrared (NIR) quantum cutting (QC) from the phosphors was observed, which involved the emission of two low-energy NIR photons (around 971 nm) from an absorbed ultra-violet (UV) photon at 358 nm via a cooperative energy transfer (CET) from Ce3+ to Yb3+ ions. The theoretical quantum efficiency was calculated and the maximum efficiency approached up to 164% before reaching the critical concentration quenching threshold. Our results demonstrated that these phosphors might find potential application in improving the efficiency of silicon based solar cells.     

Bifunctional luminescent and magnetic core/shell type nanostructures Fe3O4@CeF3：Tb^3＋/SiO2

A facile co-precipitation and microemulsion methods were applied to obtain core/shell type nanoparticles.Cerium fluoride doped with terbium(III) ions supplied intensive green luminescence of the system.Due to the presence of magnetite nanoparticles as cores,the prod-uct was highly sensitive to external magnetic field.Both sorts of nanostructures were encapsulated by silica shell.Such external layer of inert oxide can potentially increase the resistance of prepared nanostructures to thermal oxidation,aggressive agents,changing of pH or destructive radiation.Morphology of the product was examined using transmission electron microscopy(TEM) .Formations of the core/shell type nanos-tructures were clearly seen in the TEM pictures.Powder X-ray diffraction(XRD) confirmed the structure of the products,their nanocrystallin-ity and amorphous nature of silica shell.Optical properties were investigated by measuring excitation and emission spectra.Such multifunctional luminescent and magnetic nanoparticles coated with easily functionalized silica shell could be applied in many field of science.     

Magnetocaloric effect and magnetic properties of La_（0.9）Ce_（0.1）（Fe_（0.99）Mn_（0.01））_（11.6）Si_（1.4）H_（1.6） compound

Magnetocaloric effect and magnetic properties of La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4 and its hydride La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4H1.6 were investigated. The Curie temperature of La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4 was increased by hydrogen absorption. XRD patterns showed that the structure of La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4H1.6 remained NaZn13-type. The Curie temperature (TC) of the sample was increased from 174 K to 331 K. The homogeneity of the hydrogen absorption for La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4H1.6 was proven very well by the random measurement of DSC. The magnetic entropy △SM of La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4H1.6 had peak at 326 K. The peak value of-△SM-was 12.3 and 7.8 J/(kg.K) under magnetic field change of 0-2 T and 0-1 T,respectively,which was comparable with Gd5Si2Ge2. The negative slope and inflection point of the Arrott curve indicated that the first-order magnetic transition of La0.9Ce0.1(Fe0.99Mn0.01)11.6Si1.4 was reserved after hydrogen absorption.     

Tunable color emission in K3Gd（PO4）2:Tb3+,Sm3+ phosphor for n-UV white light emitting diodes

A series of K3Gd(PO4)2:Tb3+,Sm3+ phosphors were synthesized through solid state reaction. By co-doping Tb3+ and Sm3+into K3Gd(PO4)2 host and singly varying the doping concentration of Sm3+, tunable colors from green to yellow and then to orange were obtained in K3Gd(PO4)2:Tb3+,Sm3+ phosphors under the excitation at 373 nm. The energy transfer process from Tb3+ to Sm3+ was verified through luminescence spectra and fluorescence decay curves. Moreover, the energy transfer mechanism was demonstrated to be the quadrupole-quadrupole interaction. The results indicated that K3Gd(PO4)2:Tb3+,Sm3+ phosphors could be a potential application for n-UV white light emitting diodes.     

Specific features of Eu~(3+) and Tb~(3+) magnetooptics in gadolinium-gallium garnet (Gd_3Ga_5O_(12))

We reported magnetooptical properties of Eu3+(4f(6)) and Tb3+(4f(8)) in single crystals of Gd3Ga5O12 (GGG), Y3Ga5O12 (YGG), and Eu3+(4f(6)) in Eu3Ga5O12 (EuGG) for both ions occupying sites of D2 symmetry in the garnet structure. Absorption, luminescence, and magnetic circular polarization of luminescence (MCPL) spectra of Tb3+ in GGG and YGG and absorption and magnetic circular dichroism (MCD) of Eu3+ in EuGG were studied. The data were obtained at 85 K and room temperature (RT). Magnetic susceptibility of...     

Photoluminescent properties of LaF3：Eu^3＋ and GdF3：Eu^3＋ nanoparticles prepared by co-precipitation method

LaF₃:Eu³⁺ and GdF₃:Eu³⁺ nanoparticles were prepared by a co-precipitation method in the presence of the chelating agent, citric acid. The structural properties of the products were characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). The average crystallite size was estimated from the full-width at half-maximum (FWHM) of the diffraction peaks by the Scherrer equation. The sizes of the nanoparticles were 12 nm for LaF₃:Eu³⁺ and 17 nm for GdF₃:Eu³⁺. The luminescent properties of the nanoparticles were investigated by excitation and emission spectra. Energy transfer from Gd³⁺ to Eu³⁺ was observed.     

Emission of Rare Earth Complex Tb0.5Eu0.5 （asprin）3phen

The coprecipitate Tho.sEuo.5(asprin)3phen was synthesized. By doping the rare earth complex into polymer PVK, the EL device was fabricated with the structure of ITO/PVK: RE/PBD/AI. Compared with the device using PVK/Eu (asprin)3phen blend as the light emitting layer, the emission of Eu^3 in the PVK/Th0.5Eu0.5(asprin)3 phen blend is great-ly enhanced along with the quenching of the emission of PVK.     

Flux and concentration effect on Eu^3＋ doped Gd2（MoO4）3 phosphor

A novel red emitting phosphor Gd2（MoO4）3：Eu^3＋ was prepared by solid reaction, using Gd2O3, Eu2O3 and WO3 as starting matedals and NH4F as flux. The effects of flux content and Eu^3＋ concentration on the crystal structure, morphology and luminescent properties were investigated using XRD, SEM and fluorescent spectrum measurement. The XRD patterns showed that the resultants had the monoclinic structure. With the increase in flux amount, their crystallization significantly improved. The SEM images indicated that the mean size of the phosphor particles was around 2 μm, and agglomeration of the phosphor particles appeared while introducing higher flux amount. The excitation spectra exhibited more intense f-f transitions originating from ground state 7^F0 to upper states 5^L6 and 5^D2 than the charge transfer band. The concentration quenching of Eu^3＋ emission indicated that energy transfer from Eu^3＋ to molybdate host existed even at lower Eu^3＋ concentration.     

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 Characterization of Gd3Sc2Ga3O12 Polycrystalline Material by Co-Precipitation Method

Gd3Sc2Ga3O12 polycrystalline material for single crystal growth was prepared with Ga, Gd2O3 and Sc2O3 as starting materials and aqueous ammonia as the precipitator by co-precipitation method. The precursors sintered at various temperatures were characterized by infrared spectra （IR）, X-ray diffractometry （XRD） and transmitted electron microscopy （TEM）. The results showed that pure GSGG phase could be obtained at 900 ℃. The sintered powders were well-dispersed and less-aggregated in the sintered temperature range of 900 - 1000 ℃. XRD and TEM show that the polycrystalline particle sizes of the polycrystalline powders were about 20 - 50 nm. Compared with the method that Ga2O3, Gd2O3 and Sc2O3 were mixed directly and sintered to get polycrystalline materials, the synthesized temperature was lower and sintered time was shorter. Thus co-precipitation was a good method to synthesize GSGG polycrystalline material.     

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.     

Novel phosphors of Eu^3＋, Tb^3＋ or Tm^3＋ activated LaBGeO5

Rare earth borogermanates as a group of stable compounds provided various potential properties important for modern sciences. Among the properties of interests, luminescence was manifested due to the variability of rare earth elements and the compounds constituted an important group of potential candidate. In this work, novel phosphors of Eu³⁺, Tb³⁺ or Tm³⁺ doped LaBGeO₅ with the stillwellite type structure were synthesized by the solid state reaction method. Their X-ray and UV excitation luminescent properties showed that LaBGeO₅ was an excellent host lattice for the luminescence of Eu³⁺, Tb³⁺ and Tm³⁺. The LaBGeO₅:Eu³⁺, LaBGeO₅:Tb³⁺ and LaBGeO₅:Tm³⁺ presented bright red, green and blue emission light for both UV and X-ray excitation.     

A blue luminescence glass-ceramics of Eu^2＋ ions activated Li2O-BaO-B2O3

New blue luminescence glass-ceramic samples were prepared in air by annealing of the Eu^3＋-doped Li2O-BaO-B2O3 glass. The as-made glass samples only showed the sharp emission peaks assigned to the transitions of 5^D0-7^Fj （J=0, 1, 2, 3, 4） of Eu^3＋ ions. The glass-ceramic samples gave a strong and broad emission band peaking at about 382 nm ascribed to the 5d-4f transition of Eu^2＋ ions. The optical properties such as excitation and emission spectra, and the decay time of the Eu^2＋ ions were investigated in the glasses or the glass-ceramics samples. The X-ray diffraction pattern showed that LiBan9O15 might be demonstrated to be the crystallites in the glass-ceramic, which contributed to the blue luminescence. SEM micrograph was investigated on the glass-ceramic samples obtained by crystallization of the glass matrix resulting in a mixture of poly-crystals.     

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.