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%.     

Asymmetry ratio as a parameter of Eu3+ local environment in phosphors

Study of the local environment of certain ion is quite a complex problem. Due to the unique luminescent properties, Eu³⁺ ions can be used as a structural probe. In this paper, effect of doping concentration, excitation wavelength and excitation mechanism on asymmetry ratio was systematically studied using Y₃Al₅O₁₂:Eu³⁺, YVO₄:Eu³⁺ and Y₂O₃:Eu³⁺nanophosphors. The asymmetry ratio gives information about the local surrounding and environmental changes around the Eu³⁺ ions. Asymmetry ratios of YAG:Eu³⁺ and YVO₄:Eu³⁺ nanopowders were calculated using standard technique and the obtained average values were found to be 0.75 and 8.2, respectively. However, it is found that standard method of asymmetry ratio calculation is suitable only for samples where all Eu³⁺ ions occupy one site. The “multisite model” of asymmetry ratio calculation was developed and used for Y₂O₃:Eu³⁺ nanocrystalline powders. Average value of asymmetry ratio for Eu³⁺ ions occupied “normal” sites is 6.0 and for Eu³⁺ ions occupied “defect” sites is 2.3.     

Photoluminescent properties of Eu3＋ and Tb3＋ codoped Gd2O3 nanowires and bulk materials

In this paper, the Gd2O3：Eu3＋,Tb3＋phosphors with different doping concentrations of Eu3＋and Tb3＋ions were prepared by a hydrothermal method for nanocrystals and the solid-phase method for microcrystals. The interaction of the doped ions with different concentrations and the luminescent properties of the nanocrystals and microcrystals were studied systematically. Their structure and morphology of Gd2O3：Eu3＋,Tb3＋phosphors were analyzed by means of X-ray powder diffraction （XRD）, transmission electron mi-croscopy （TEM） and scanning electron microscopy （SEM）. The photoluminescence （PL） properties of Gd2O3：Eu3＋,Tb3＋phosphors were also systematically investigated. The results indicated that when the concentration of doped Eu3＋was fixed at 1 mol.%, the emis-sion intensity of Eu3＋ions was degenerating with Tb3＋content increasing, while when the Tb3＋content was fixed at 1 mol.%, the emission intensity of Tb3＋ions reached a maximum when the concentration of Eu3＋was 2 mol.%, implying that the energy transfer from Eu3＋to Tb3＋took place. In addition, Tb3＋could inspire blue-green light and the Eu3＋could inspire red light. Therefore co-doping systems by controlling the doping concentration and the hosts are the potential white emission materials.     

A green-yellow emitting β-SreSiO4：Eu^2＋ phosphor for near ultraviolet chip white-light-emitting diode

Sr2SiO4：xEu^2＋ phosphors were synthesized through the solid-state reaction technique. The crystal phase of Sr2SiO4：xEu^2＋ phosphor manipulated by Eu^2＋ concentration was studied. The phase transited from β to α＇ in Sr2SiO4：xEu^2＋ phosphor with increasing europium concentration. The single β phase was formed as x≤005 and changed α＇ phase when x〉0.01. The emission spectrum of the β-Sr2SiO4：Eu^2＋ phosphor consisted of a green-yellow broadband peaking at around 540 nm and a blue band at 470 nm under near ultraviolet excitation. The white LEDs by combining near ultraviolet chips with β-Sr2SiO4：Eu^2＋ phosphors were fabricated. The luminous efficiency （15.7lm/W） was higher than α＇-Sr2SiO4：Eu^2＋ phosphor white LED.     

Optical and scintillation properties of Bi4Si3O12:RE (RE=Eu3+, Sm3+, Ho3+, Tb3+) single crystals

Bi_4 Si_3 O_(12):RE(BSO:RE, RE = Eu~(3+), Sm~(3+), Ho~(3+), Tb~(3+)) crystals were grown by the modified vertical Bridgeman method, and doping effects on scintillation properties were investigated. Under γ-ray irradiation, the light yield of BSO doped with small doses of Eu~(3+) increases slightly, and the energy resolution improves significantly compared to pure BSO, therefore the ability of distinguishing between particles will be improved for BSO crystals with a small amount of Eu~(3+) dopant. The results show that a small amount of Eu~(3+) doping can sensitize the Bi~(3+) ions. The sensitization effect enables the reduction of intrinsic defects, and thus improves the scintillation properties. However, the relative light yield of BSO:Tb(1.0 mol%) crystal is 4.3%, which is smaller than 5.0% of pure BSO. The improved light yield and energy resolution in the BSO:Eu and BSO:Sm crystals are considered an impressive achievement in the optimization of this scintillator which is already suitable for applications such as dual-readout calorimeters and homogeneous hadron calorimeters.     

Shape control over microwave hydrothermally grown Y2O3:Eu by europium concentration adjustment

Two-step synthesis of Y2〇3:Eu nanostructures was performed. It includes microwave driven hydrothermal and calcination stages. Performed route results in crystallization of Y4〇(OH)g(N〇3):Eu crystals initially, then Y2〇3:Eu crystals after calcination. Arranged Eu contents in relation to overall cation quantity were set to 2 mol%, 10 mol% and 20 mol%. Varying europium concentrations influence habit of obtained Y4〇(OH)g(N〇3):Eu crystals from needle-like to plate-like and as a result, also shapes of final Y2〇3:Eu nanostructures. Additionally, certain amount of Eu2+ ions was detected in as-grown material using laser spectroscopy and decay kinetics measurements. Obtained material was calcined at 1200 °C in the air, which results in oxidation of Eu2+ ions and crystallization of small number of cubic EU2 O3 nanocrystals. Characterization of obtained materials was performed using XRD, SEM, TEM, EDX, CL,Raman and photoluminescence spectroscopy.     

Luminescent properties of Eu3+-doped BaZrO3 phosphor for UV white light emitting diode

A novel orange phosphor Eu³⁺ doped barium zirconate (BaZrO₃) was synthesized by conventional solid state reaction method and its crystal structure and luminescent properties were investigated in this paper. The X-ray diffraction patterns (XRD) showed that simple BaZrO₃ phase was obtained. Monitoring at 596 nm, the excitation spectrum consisted of a broad band and a series of narrow bands and the stronger excitation peaks located at 275 and 393 nm, respectively. The emission spectrum excited by 393 nm UV light was composed of four narrow bands. The strongest emission was located at 596 nm. The appropriate concentration of Eu³⁺ was 0.025 (molar fraction) for the highest emission intensity at 596 nm. The H₃BO₃ and ammonium were added as flux and the results showed that 2 wt.% NH₄F ions was the optimal flux for BaZrO₃:Eu³⁺.     

A single-phase full-color phosphor Sr2Ca2La(PO4)3O:Eu2+,Tb3+,Mn2+: Photoluminescence and energy transfer

A single-phase full-color emitting phosphor Sr₂Ca₂La(PO₄)₃O:Eu²⁺,Tb³⁺,Mn²⁺ was synthesized by the high temperature solid-state method. The phase formation, luminescence properties, thermal stability, and energy transfer from Eu²⁺ to Tb³⁺ and Eu²⁺ to Mn²⁺ in Sr₂Ca₂La(PO₄)₃O were investigated in details. Tunable emission color from blue to blueish green or orange can be observed under 365 nm near-ultraviolet excitation based on the energy transfer from Eu²⁺ to Tb³⁺ or Mn²⁺ ions by varying the ratio of Eu²⁺/Tb³⁺ or Eu²⁺/Mn²⁺ ions. White light was obtained with chromaticity coordinates of (0.3558, 0.3500) in the Sr₂Ca₂La(PO₄)₃O:0.04Eu²⁺,0.08Tb³⁺,0.40Mn²⁺ phosphor, suggesting their potential applications in white light emitting diodes.     

Preparation and photoluminescence enhancement of Li＋ and Eu3＋ co-doped YPO4 hollow microspheres

Li+ and Eu3+ co-doped YPO4 hollow microspheres were successfully synthesized by a sacrificial template method using polystyrene (PS) as template. Techniques of X-ray diffraction (XRD), scanning electron microscopy (SEM), as well as transmission electron microscopy (TEM) were employed to characterize the as-synthesized sample. Furthermore, the photoluminescence (PL) characterization of the Li+ and Eu3+ co-doped YPO4 microsphere was carried out and the effects of the doping concentration of Li+ and Eu3+ active center concentration as well as calcination temperature on the PL properties were studied in detail. The results showed that the incorporation of Li+ ions into the YPO4 :Eu3+ lattice could induce a remarkable improvement of the PL intensity. The highest emission intensity was observed with the compound of 5%Li+ and 5%Eu3+ co-doped YPO4 , whose brightness was increased by a factor of more than 2.2 in comparison with that of the YPO4 :5%Eu3+.     

Synthesis and luminescence properties of a novel red-emitting phosphor SrCaSiO_4：Eu~（3＋） for ultraviolet white light-emitting diodes

A novel red phosphor based on Eu3+-activated SrCaSiO4 was successfully synthesized by conventional solid state reaction method and the photoluminescence properties were investigated. X-ray diffraction (XRD) patterns indicated that SrCaSiO4:Eu3+ phosphors belong to orthorhombic crystal system (space group=Pmnb). The photoluminescence (PL) excitation spectrum showed broad-band absorption and the strongest excitation peak at 397 nm contributed to the 7F0→5L6 transition which matched well with the emission of a...     

Nano-preparation promoting effectively luminescent properties of one-dimensional rare earth oxides

Rare earth (La,Nd and Tb) oxides with one-dimensional micro/nanostructures were synthesized hydrothermally under facile and mild conditions with two surfactants, and characterized by X-ray diffraction (XRD), thermal gravimetry (TG), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and photoluminescence. The results showed that the synthesized rare earth oxides behaved regular nano-and micro-scale structures. And the morphologies of samples depended on the radii of rare earth ions, with the help of two surfactants of sodium dodecyl sulfonic and PEG 600. Nanocrystalline La2O3:Eu3+ possessed good photoluminescence (PL) property and might be used as a nanosized phosphor, its PL intensity was altered by the doping Eu3+ concentration and the optimum concentration of Eu3+ was 3 mol.%. In comparison with bulk Eu3+/La2O3, Eu3+/nano-La2O3 showed better photoluminescence property, nearly equal to that of nanocrtstal-line La2O3:Eu3+. Tb4O7 microwires showed interesting photoluminescence properties.     

Comparative Study on Photoluminescent Properties of CaGdAlO4：Eu3＋ Phosphors Synthesized with Three Methods

CaGdAlO4 ： Eu^3＋ powder phosphors were prepared using citrate sol-gel （CSG）, haft-dry and half-wet （HDW） and solid state （SS） methods, respectively. X-ray diffraction results confirm the formation of CaGdAlO4：Eu^3＋ at 900 % （CSG）, 1200℃ （HDW） and 1400℃ （SS）, respectively. Field emission scan electron microscopy （FE-SEM） images show that the CaGdAlO4：Eu^3＋ powder prepared by the CSG and HDW method has an elliptical shape and that prepared under the SS method has a flaky shape. Upon excitation with 280 nm UV light, all the CaGdAlO4： Eu^3＋ powders show bright red emission on account of the 4f-4f transitions of the Eu^3＋ ions. Moreover, the size of the phosphor particles and the emission intensity increase with the increase of calcined temperature. At the same calcination temperature of 1400 ℃, the ^5D0→^7F2 emission intensity of the sample prepared by HDW method is the highest. Stark components of the ^5D0→^7FJ emission transitions, both at room temperature and at a low temperature, reveal that the Eu^3＋ ions occupy only one site with non-centrosymmetry in the crystals.     

Upconversion multicolor tuning of NaY(WO4)2:Tb3+ with Eu3+ doping

A series of Tb~(3+) and Eu~(3+) co-doped NaY(WO_4)_2 phosphors were synthesized by hydrothermal reactions.The crystal structure,morphology,upconversion luminescent properties,the energy transfer from Tb~(3+) to Eu~(3+)ions and the ~5 D_4→ ~7 F_5 transition of the Tb~(3+) ion in NaY(WO_4)_2:Tb~(3+),Eu~(3+) phosphors were investigated in details.The results indicate that all the synthesized samples are of pure tetragonal phase NaY(WO_4)2.Furthermore,the micrometer-sized needle spheres and excellent dispersion of the particles are obtained by adding polyethylene glycol(PEG-2000) as the surfactant.Phosphors of NaY(WO_4)_2:Tb~(3+),Eu~(3+) exhibit the492 nm blue emission peak,546 nm green emission peak,595 nm orange emission peak and 616 nm red emission peak under 790 nm excitation.The energy transfer from Tb~(3+) to Eu~(3+) is a resonant transfer,in which electric dipole-dipole interaction plays a leading role.By adjusting the doping concentration of Eu~(3+) in NaY(WO_4)_2: 1.0 mol%Tb~(3+),xmol%Eu~(3+) phosphors,the emitting color of UC phosphors can be tuned from green to red.     

Structure and luminescent properties of luminous polypropylene fiber based on Sr2MgSi2OT：EU^2＋,Dy^3＋

The luminous polypropylene fiber based on long afterglow luminescent material Sr2MgSi2O7：Eu^2＋,Dy^3＋was prepared by melt-spinning process. Micro-morphology, phase composition, crystal structure, spectral features and afterglow properties of the lu-minescent fiber were tested and analyzed. The results indicated that the fiber had independent superposition phase features of both Sr2MgSi2O7：Eu2＋,Dy3＋and polypropylene. The range of its excitation wavelength was located between 250-450 nm;therefore, the luminescent fiber could be excited by ultraviolet or visible light. It could emit blue light of 460 nm wavelength after excitation, which was caused by the 5d-4f transition of Eu^2＋ions within the host lattice. The initial luminescent intensity was more than 0.8 cd/m^2, and afterglow life lasted 7 h. The afterglow decay was composed of rapid-decaying and slow-decaying processes, and the decay charac-teristics depended on the depth and concentration of trap level in the Sr2MgSi2O7：Eu^2＋,Dy^3＋.     

Red-emitting CaWO4:Eu3+,Tm3+ phosphor for solid-state lighting: Luminescent properties and morphology evolution

CaWO₄:xEu³⁺,yTm³⁺crystals were obtained by facile synthesis at low temperature by the microwaveassisted hydrothermal method(MAH).The phase formation,morphology,luminescent properties and ene rgy transfer were investigated.The X-ray diffraction(XRD)re sults show the formation of a scheelitelike tetragonal structure without the presence of secondary phases.The growth mechanism of hierarchical micro structures based on self-assembly and Ostwald-ripening processes was evaluated,obtaining different types of morphologies.The luminescence spectra of CaWO₄:Eu³⁺,Tm³⁺at 325 nm excitation show the predominance of red emission at the 5 D0→7 F2(Eu³⁺)transition at 624 nm.This feature signals dominant behavior of the electric dipole type.The presence of Tm³⁺is notably evident in the absorption spectra by the related excitation transitions:3 H6→1 G4,3 H6→3 F3 and 3 H6→3 H4.Color parameters are discussed to characterize CaWO₄:Eu³⁺,Tm³⁺emission.The study of the emission spectrum as a function of the concentration of Eu³⁺(x mol%)and Tm³⁺(y mol%)indicates that the CaWO₄:Eu³⁺,Tm³⁺phosphors show stronger red emission intensity and exhibit the CIE value of x=0.63 and y=0.35.The photoluminescence results show 97%high color purity for CaWO₄:4 mol%Eu³⁺,a high CRI(92%)and a low CCT of 1085 K.These results demonstrate that the CaWO₄:Eu³⁺,Tm³⁺red phosphors are promising as color converters for application in white light-emitting diodes and display devices.     

Intense blue-emitting Ca2PO4Cl:Eu2+ phosphor for near-ultraviolet converting white light-emitting diodes

A blue phosphor Ca₂PO₄Cl:Eu²⁺ (CAP:Eu²⁺) was synthesized by solid state reaction. The Ca₂PO₄Cl:Eu²⁺ exhibited high quantum efficiency and excellent thermal stability. The luminescent intensity of Ca₂PO₄Cl:Eu²⁺ was found to be 128% under excitation at 380 nm, 149% under 400 nm, and 247% under 420 nm as high as that of BaMgAl₁₀O₁₇:Eu²⁺. The optimal doping concentration was observed to 11 mol.% of CAP:Eu²⁺. The energy transfer between Eu²⁺ ions in CAP were occurred via electric multipolar interaction, and the critical transfer distance was estimated to be 1.26 nm. A mixture of blue-emitting Ca₂PO₄Cl:Eu²⁺, green-emitting (Ba,Sr)₂SiO₄:Eu²⁺ and red-emitting CaAlSiN₃:Eu²⁺ phosphors were selected in conjunction with 400 nm chip to fabricate white LED devices. The average color-rendering index R_a and correlated color temperature (T_c) of the white LEDs were found to be 93.4 and 4590 K, respectively. The results indicated that it was a promising candidate as a blue-emitting phosphor for the near-UV white light-emitting diodes.     

Single-phase white-emitting and tunable color phosphor Na3Sc2(PO4)3:Eu2+,Dy3+: Synthesis,luminescence and energy transfer

A series of Eu²⁺/Dy³⁺ single doped and co-doped Na₃Sc₂(PO₄)₃ phosphors were synthesized by the high-temperature solid-state method, and their phase, morphology, and luminescence properties were characterized. Under the excitation of 370 nm, the Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor can emit white light whose spectrum is composed of a broad emission band centered at 460 nm and the other three peaks at 483, 577, and 672 nm, respectively. There is energy transfer from Eu²⁺ to Dy³⁺ ion in Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor due to the good overlap between the emission spectrum of Na₃Sc₂(PO₄)₃:Eu²⁺ and the excitation spectrum of Na₃Sc₂(PO₄)₃:Dy³⁺, which is further confirmed by the fluorescence lifetime decrease of Eu²⁺ ion with the increase of Dy³⁺ concentration. The process of energy transfer is via dipole–quadruple interaction which is confirmed by applying Dexter's theory. By increasing the Dy³⁺ concentration, the color coordinates of the Na₃Sc₂(PO₄)₃:0.01Eu²⁺,xDy³⁺ phosphors can be adjusted from blue to white, and then to yellow. The optimized concentration of Dy³⁺ ions is 4.0 mol%, beyond which the concentration quenching will take place. The Na₃Sc₂(PO₄)₃:Eu²⁺,Dy³⁺ phosphor shows fairly good resistance to thermal quenching behavior, of which the emission intensity at 423 K can maintain 90.3% of the initial value (298 K). These results suggest that the Na₃Sc₂(PO₄)₃:0.01Eu²⁺,xDy³⁺ phosphors have potential applications as the color-tunable or a single-phase white emitting phosphor in white LEDs.     

Preparation,structure, luminescence properties of europium doped zinc spinel structure green-emitting phosphor ZnAl2O4:Eu2+

The Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders were synthesized by the solid-state reaction method.The synthesis temperature for ZnAl_2 O_4 was optimized,whereas the phase structure,TEM images,photoluminescence(PL) properties,the concentration quenching mechanism,the fluorescence decay curves,as well as the CIE chromaticity coordinates of the samples were investigated in details.Under the excitation at 379 nm,the phosphor exhibits an asymmetric broad-band green emission with a peak at 532 nm,which is ascribed to the 5 d-4 f transition of Eu2+.When the doping concentration of Eu2+ ions is 0.01,the luminescence intensity of the sample reaches the maximum value.It is further proved that the exchange interaction results in the concentration quenching of Eu2+ in the Zn_(1-x)Al_2 O_4:xEu~(2+) phosphor powders.The thermal quenching property of ZnAl_2 O_4:Eu~(2+)phosphor was investigated and the quantum efficiency(QE) values of the selected Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) phosphor was measured and determined as 54.85%.The lifetime of the optimized sample Zn_(0.99)Al_2 O_4:0.01 Eu~(2+) is 3.0852 μs and the CIE coordinate of the sample was calculated as(0.3323,0.5538) with high-color-purity green emission.All properties indicate that the green-emitting ZnAl_2 O_4:Eu~(2+) phosphor powder has potential application in white LEDs.     

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.     

Enhanced afterglow performance of CaAl_2O_4:Eu~(2+),Nd~(3+) phosphors by co-doping Gd~(3+)

In order to effectively improve the afterglow properties of CaAl_2 O_4:Eu~(2+),Nd~(3+) phosphors,a series of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)(x=0,0.012,0.024,0.036,0.048,0.060 mol) phosphors were prepared by a high-temperature solid-phase approach.Crystalline composition and microstructure were characterized by XRD,TEM,HRTEM,and XPS,luminescence properties were systematically analyzed by fluorescence spectra,afterglow decay curves and TL glow curve.Results show that all of Ca_(0.982-x)Al_2 O_4:0.012 Eu~(2+),0.006 Nd~(3+),xGd~(3+)phosphors belong to monoclinic CaAl_2 O_4,without other cystalline phase.The blue emission at 442 nm is observed,which is assigned to the 4 f~65 d→4 f~7 transition of Eu~(2+) ions.Doping with appropriate amount of Gd~(3+) ions(x=0.036 mol) significantly improves the afterglow properties of phosphors,but the excessive doping of Gd~(3+) induces the fluorescent quenching.The doping of moderate Gd3+changes the traps states,the trap depth varies from 0.598 to 0.644 eV and the trap concentration is also greatly improved,thus significantly improving afterglow performance.