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1.
Nanosized Gd2(1-x)Eu2xTi2O7:yV5+ phosphors were prepared via sol-gel method and characterized with X-ray diffraction,Raman spectroscopy,diffuse reflectance spectra and photoluminescence spectra.Their PL properties were investigated as functions of the Eu3+ doping concentration and annealing temperature.The results indicated that the as-prepared samples showed a strong emission of Eu3+ under the irradiation of 303 nm.For Eu3+-doped Gd2Ti2O7,the orange emission at 586 nm was the strongest,which was correspond...  相似文献   

2.
In the present work,a sol-gel method was employed to prepare nanosized SrAl2O4 powders doped with Eu3+ ions.The raw nano-materials were thermally treated at 900 to 1100 oC for 3 h.The XRD analysis demonstrated that the powders were single-phase nanopowders with high crystallite dispersion.Our studies were focused on relating the luminescence properties of the Eu3+ dopant to the NC(nanocrystal-lites) size.This was achieved by varying the calcinations temperature between 900 and 1100 oC.The average NC size varied accordingly be-tween ~36 and ~75 nm.We found that size effect manifested mainly in the expansion of the cell volume and broadening of XRD peaks as in-dicated by Rietveld analysis.Moreover the emission and excitation spectra,although typical for Eu3+ ions,demonstrated some degree of variability with calcinations temperature and doping concentration.To explain these differences a detailed analysis of luminescence spectra by the Judd-Ofelt theory was performed.  相似文献   

3.
One-dimensional Lu2O3:Eu3+ nanofibers were prepared by electrospinning followed by high-temperature calcinations.Thermogravimetric and differential thermal analysis,X-ray powder diffraction,Fourier transform infrared spectroscopy,scanning electron microscopy,photoluminescent spectra and decay curves were used to characterize the samples.Results showed that samples began to crystallize at ~500 oC and crystallized completely around 1000 oC.The average diameter of nanofibers(1000 oC annealed) was about 55 nm and the particle size of Lu2O3:Eu3+ increased with increasing annealing temperature.Under ultraviolet excitation,nanofibers exhibited typical red emission of Eu3+ in Lu2O3.The effect of heat-treatment temperature on luminescent properties of nanofibers was also discussed.  相似文献   

4.
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+.  相似文献   

5.
YAl3 (BO3)4: Eu3 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: Eu3 phosphors with concentration of Eu3 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 re- gion. In the emission spectra, the peak wavelength was about 614 nm under a 252 nm UV excitation. The optimal doping concentration of Eu3 ions in YAl3(BO3)4: Eu3 phosphors was 8 mol%.  相似文献   

6.
The novel phosphors of La 2 MoO 6 activated with the trivalent rare earth Ln 3+ (Ln=Eu, Sm, Dy, Pr, Tb) ions were synthesized by solid state reactions at high temperature in air atmosphere, and their phase impurities and luminescent properties were studied. The photoluminescence (PL) excitation and emission spectra, and decay curves were employed to study their luminescence properties. The lifetimes of the characteristic emissions from Ln 3+ ions were in the order of millisecond except Pr 3+ ions. (LaEu 1-x ) 2 MoO 6 was a promising phosphor for practical application and the optimum concentration was x=0.075. The concentration quenching mechanism of Eu 3+ was also discussed by theoretical fitting using Burshtein model.  相似文献   

7.
Nanowires/nanorods of europium/terbium orthophosphate monohydrate with Eu3+ concentration of 6,11,and 20 at.% were prepared by microwave synthesis method.The effects of Eu3+ doping concentration on structure,morphology and optical properties of nanoma-terials were also investigated.The results showed that,for all studied Eu3+ doping concentrations,a single-crystalline phase of rhabdo-phane-type(Eu,Tb) PO4·H2O nanowires/nanorods was obtained by using microwave heating of an aqueous solution of terbium(III) nitrate,europium(III) nitrate and NH4H2PO4 with pH=2.The length and width of these nanowires/nanorods ranged from 150 to 300 nm and from 10 to 50 nm,respectively.The evidence of energy transfer from Tb3+ to Eu3+ due to the energy overlap between the donor Tb3+ and the acceptor Eu3+ was observed obviously via a significant enhancement in the luminescent intensity of Eu3+.  相似文献   

8.
ZnTiO3:Eu3+ phosphors were synthesized with different concentrations of Eu3+ doping through sol-gel method. The samples were calcined at different temperatures for 2 h in air. The synthesized powders were characterized by X-ray diffraction(XRD), scanning electron microscopy-energy dispersive spectroscopy(SEM-EDS), transmission electron microscopy(TEM), Raman and photoluminescence spectroscopy. The XRD results showed that the Zn Ti O3:Eu3+ phosphors doped with different concentrations of Eu3+ ions calcined at 600 oC were of single phase, which indicated that the Eu3+ ions had been successfully incorporated into the Zn Ti O3 host lattice and did not destroy the lattice structure of Zn Ti O3 host. The Raman spectrum, SEM and TEM also proved that the doping of Eu3+ did not change the lattice structure of hexagonal Zn Ti O3 host. The photoluminescence(PL) of Eu3+ ions with the main emission peak at 614 nm was observed to increase with Eu3+ concentrations from 0.5 mol.% to 2.0 mol.% and decreased when the concentration was increased to 2.5 mol.%. The decrease in the PL intensity at higher Eu3+ concentrations could be associated with concentration quenching effect. The CIE1931 chromaticity diagram(x, y) of Zn Ti O3:2.0 wt.%Eu3+ phosphors were located in the red region(x=0.652, y=0.347). The luminescence properties suggested that Zn Ti O3:Eu3+ phosphors might be regarded as a potential red phosphor candidate for light emitting diodes(LEDs).  相似文献   

9.
Eu2+-doped K2 Mg Si3O8 phosphors were synthesized by conventional solid-state reaction method. The phase formation of as-prepared samples was characterized by X-ray powder diffraction. The luminescence properties were investigated by the photoluminescence excitation and emission spectra, decay curve and CIE coordinates. The phosphor showed bluish-green emission centered at 460 nm under the excitation of UV and near UV light with the wavelength range of 250–430 nm. Two Eu2+ emission centers existed in the K2 Mg Si3O8:Eu2+ phosphor according to the luminescence spectra and the decay curves. The critical quenching concentration of Eu2+ doping was determined to be 3.0 mol.% and the concentration quenching mechanism was dipole-dipole interactions between Eu2+ ions. These results suggested that K2 Mg Si3O8:Eu2+ was a potential bluish-green phosphor candidate for white UV-LED.  相似文献   

10.
An improved sol-gel method was employed to prepare Eu3+ ions doped SiO2-Y2O3 nanocomposites.Systematic study was carried out on the effect of post-annealing treatment on photoluminescence(PL) properties of the samples under various europium ions doping concentrations.X-ray diffraction(XRD) patterns indicated that the samples showed an amorphous matrix structure,and the scanning electron microscopy(SEM) pictures showed that the samples presented a nano size(from 21 to 42 nm) granular-stack structure after high-temperature annealing treatment(from 600 to 900 °C,respectively) for 3 h.Raman spectra demonstrated that Y3+ and Eu3+ ions were incorporated into the composites through the sol-gel and post-annealing process.Under the excitation of 394 nm(7F0→5L6) light,red emission was observed around 613 nm(5D0→7F2).Without annealing treatment,the optimized doping amount of Eu ions was about 6.5 mol.%,which was much higher than that single doped in SiO2 glass matrix with Eu ions concentration of 3%,and it raised to 9.0% when the samples were annealed at high-temperature(900 °C) annealing.  相似文献   

11.
Three new rare earth ternary complexes,RE(PPP)3bpy(RE=Sm 3+ ,Eu 3+ ,Tb 3+ ),were synthesized by the reaction of 1-phenyl-3-(p-phenylethynylphenyl)-1,3-propanedione(HPPP)and 2,2′-bipyridine(bpy)with rare earth chloride RECl3,respectively,in alcohol solution. The compositions were characterized by means of infrared(IR)spectra,chemical analysis,elemental analysis,and thermodynamic analysis.Luminescent properties of the three complexes were studied.At room temperature,under UV light excitation,the Sm 3+ ,Eu 3+ and Tb 3+ complexes exhibited characteristic emission of the central ions.The fluorescence spectra showed that the fluorescence emission intensity of Eu 3+ complex was the strongest.The narrow strongest emission band of Eu 3+ complex was considered to be a valuable material with bright red fluorescence.  相似文献   

12.
Yttrium oxide doped with europium has a great prospective for FED and PDP phosphor application. In present study, the precursor of yttrium oxide hydroxide nitrate nanorod, which was prepared via hydrothermal reaction route using PEG-6000 as template from the starting Y(NO3)3 and KOH reactant system, was used to prepare Y2O3:Eu3 nanorod via a post annealing process during which the precursor with adjustable shape and size was transformed to final Y2O3:Eu3 product. XRD, field emission scanning electron microscopy (FE-SEM) and photoluminescence spectra (PL) were used to characterize the crystalline, morphology and luminescence properties of as-formed Y2O3:Eu3 products synthesized at different post annealing temperatures, respectively. The results indicate that grain morphology of obtained Y2O3:Eu3 product was nanorod with a mean diameter of about 40~60 nm and length of about 500~700 nm, the nanorod structure and morphology of obtained Y2O3:Eu3 product maintained during post annealing process and the size varied slightly with different annealing temperatures. Pure cubic Y2O3:Eu3 phase was formed and the size was the smallest at annealing treatment of 500 ℃. Under the annealing temperature below 500 ℃ its diameter increased with increasing annealing temperature, and remained in a stable size when the annealing temperature was above 500 ℃. The PL spectra of excitation spectra of Y2O3:Eu3 product show that it exhibits excitation band located at about 395 and 468 nm, respectively. Above two excitation bands could be ascribed to the transition 4f-4f of Eu3 ions in the Y2O3 host. On the other hand, the main emission peaks of the as-prepared products could be ascribed to the Eu3 ions transition from 5D0 to 7F2. Furthermore, the luminescent intensity was improved about three times when the annealing temperature increased from 500 to 1000 ℃.  相似文献   

13.
Sr3SiO5:Eu2+ yellow phosphors for white LEDs were synthesized by high temperature solid state reaction method under a reductive atmosphere. The crystalline phases were examined with X-ray diffraction (XRD). Luminescence properties were studied, and effects of various fluxing agents BaCl2, MgF2, CaF2 and BaF2 on the emission spectra were also studied. The optimal Eu2+ concentration and flux were determined. Sr3SiO5: Eu2+ was obtained by firing the sample on optimal composition and fabrication process. The sa...  相似文献   

14.
Thermal annealing of YOH1.1F1.9 and YOH1.1F1.9:Ln3+(Ln3+=Eu3+,Tb3+ and Gd3+) precursors in air gave access to synthesize yttrium oxyfluoride phosphors with well-preserved needle-like morphologies. The phase purities of samples strongly depended on the thermal annealing temperature. At 600 °C, pure Y5O4F7 with orthorhombic structure were obtained, as evidenced by powder X-ray diffraction measurement and chemical analysis. The interesting microstructure evolution of the annealed sample from well-organized nanoparticles on curly slices to microrod-bundle structure had been aroused by raising annealing temperature. The multicolor fluorescent emissions of Y5O4F7:Ln3+ phosphors were observed, e.g. ultraviolet emission for Gd3+ , green emission for Tb3+ and red emission for Eu3+ , which resulted from characteristic transitions of different lanthanide ions.  相似文献   

15.
The effect of subcritical annealing temperature on microstructure and mechanical properties of SCM435 steel was investigated through changing the heating and soaking temperature as 660 °C, 680 °C, 700 °C, 720 °C and 745 °C. The microstructure and mechanical properties of intercritically annealed specimens were analyzed. With increasing the subcritical annealing temperature from 660 °C to 720 °C, the spheroidization ratio gradually increased, and the mechanical properties, formability and Vickers hardness were improved. According to the comprehensive comparison of mechanical properties and formability, the subcritical process at soaking temperature of 680-720 °C could achieve similar annealing effect as that of intercritical process. Therefore, the subcritical annealing temperature could be set as 700 °C in practice, with the Ac1 temperature fluctuation within ±20 °C, and the applicability and stability of subcritical annealing were guaranteed in industrial application. The plant results of the cold heading showed that the subcritical annealing could replace original intercritical annealing successfully with significantly saving time and energy.  相似文献   

16.
YVO4:Eu nanocrystalline phosphors were successfully prepared at 400 oC in equal moles of NaNO3 and KNO3 molten salts. NaOH concentration and annealing temperature played important roles in phase purity and crystallinity of the nanocrystallines, and the optimum NaOH concentration and annealing temperature were 6:40 and 400 oC, respectively. The nanocrystallines were well crystallized with a cubic morphology in an average grain size of 18 nm. Upon excitation of the vanadate groups at 314 nm, YVO4:Eu nanocrystallines exhibited the characteristic emission of Eu3+, which indicated that there was an energy transfer from vanadate groups to Eu3+. Moreover, the influence of superficial effect, especially the dangling bonds on the structure and luminescent properties of the nanocrystallines was discussed in detail.  相似文献   

17.
LiFe0.99RE0.01PO4/C cathode material was synthesized by solid-state reaction method using FeC2O4·2H2O, Li2CO3, NH4H2PO4, RE(NO3)3·nH2O as raw materials and glucose as a carbon source. The doping effects of rare earth ions, such as La3+, Ce3+, Nd3+, on the structure and electrochemical properties of LiFePO4/C cathode material were systematically investigated. The as-prepared samples were characterized by means of X-ray diffraction(XRD), scanning electron microscopy(SEM) and particle size analysis. The electrochemical properties were investigated in terms of constant-current charge/discharge cycling tests. The XRD results showed that the rare earth ions doping did not change the olivine structure of LiFePO4, and all the doped samples were of single-phase with high crystallinity. SEM and particle size analysis results showed that the doping of La3+, Ce3+ and Nd3+led to the decrease of particle size. The electrochemical results exhibited that the doping of La3+ and Ce3+ could improve the high-rate capability of LiFePO4/C cathode material, among which, the material doped with 1% Ce3+ exhibited the optimal electrochemical properties, whose specific discharge capacities could reach 128.9, 119.5 and 104.4 mAh/g at 1C, 2C and 5C rates, respectively.  相似文献   

18.
Ba0.9-ySryAl12O19:Eu0.1 phosphors were prepared by sol-gel technique,the crystalline structures of samples characterized by XRD,and the luminescence properties were investigated.The influence of crystallographic positions on the luminescent properties of Sr2+-doped BaAl12O19:Eu was investigated in detail.The results indicated that the crystal lattice of BaAl12O19:Eu was not influenced by the Sr2+ and doping Sr2+ in BaAl12O19:Eu enhanced the luminescent properties of the phosphors at the proper concentration of Sr2+.With the increasing of concentration of Sr2+ doped in BaAl12O19:Eu,the relative luminescent intensity of Ba0.9-ySryAl12O19:Eu0.1 strengthened and blue-shifted.  相似文献   

19.
Polycrystalline YBa_2Cu_3O_(6+δ) bulks were synthesized by sol-gel method. Sintering processing played a vital role in the evolution of phase structure and microstructure, and thus significantly influenced their superconducting properties. The influence of calcination temperature, sintering temperature, on the bulks structure, morphology and superconducting behaviors were investigated. The results showed that the oxygen content drastically increased with calcination temperature and sintering temperature. The SEM images revealed that the grains grew up monotonously with increase of calcination temperature. With increased calcination and sintering temperature, the resistivity was reduced gradually and the superconducting properties increased. Moreover, it was found that the optimal superconducting properties(with the highest superconducting transition temperature T_c~(onset) and the narrowest transition width ΔT) were obtained at calcination temperature of 900 °C and sintering temperature of 950 °C.  相似文献   

20.
Undoped and rare earth ions(Eu3+, Ce3+, Tb3+) doped β-Sr HPO4 nanomaterials were successfully prepared by a facile hydrothermal method. The crystal structure, morphology and luminescent properties were characterized by X-ray powder diffraction(XRD), scanning electron microscopy(SEM), transmission electron microscopy(TEM), photoluminescence(PL) spectra and luminescence decay curves. The results indicated that the undoped and rare earth ions doped Sr HPO4 nanomaterials(the doping concentration was not above 7%) were well crystallized, with the same crystal structure(β-Sr HPO4). Nevertheless, the doping of rare earth ions could lead to the changing of morphology from nanoflakes to nanocrystals. Under the excitation of UV light, rare earth ions(Eu3+, Ce3+, Tb3+) doped β-Sr HPO4 nanocrystals exhibited the characteristic emission of Eu3+, Ce3+ and Tb3+ ions, respectively. The luminescence decay curves of β-Sr HPO4:Eu3+ and β-Sr HPO4:Ce3+,Tb3+ nanocrystals conformed to the double exponential fluorescence decay, and the average lifetimes were 1.14 and 4.12 ms, respectively. The luminescence decay curve of β-Sr HPO4:Ce3+ was fitted into a single exponential function, and the lifetime was about 0.78 ns.  相似文献   

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