首页 | 本学科首页   官方微博 | 高级检索  
相似文献
 共查询到20条相似文献,搜索用时 15 毫秒
1.
Green light-emitting Ba2SiO4:Eu2+ phosphors co-doped with La or Y were synthesized by conventional solid-state reaction technique in reductive atmosphere (a mixture of 5% H2 and 95% N2). The results showed that the co-doping of La and Y could greatly enhance the fluorescence intensity of Ba2SiO4:Eu2+ phosphors. The optimum doping concentration expressed by the x value in (Ba0.985-1.5xREx)2SiO4: 0.03Eu2+ (RE=La or Y) was determined to be of 0.05. The excitation and emission peaks of all as-synthesized phosphors were wide bands. The excitation bands ranged from 250 to 400 nm, which matched well with the wavelength of near ultraviolet white light-emitting diodes (LED) chip and could be used as a potential candidate for the fabrication of white LED. The emission bands from 450 to 550 nm were typical 5d-4f transition emission of Eu2+ and displayed un-symmetry profiles because of the two substitution sites of Ba2+ with Eu2+.  相似文献   

2.
3.
Green-emitting Sr2LiSiO4F:Eu2+ and blue-emitting Sr2MgSi2O7:Eu2+ phosphors were synthesized by the conventional high temperature solid-state route,respectively.Their structures and photoluminescenee properties were comparatively investigated.It was found that the mixture phases of Sr2MgSi2O7 and SrF2 were obtained when a part of Sr2+ in Sr2LiSiO4F was replaced by some amount of Mg2+ in order to design the possible SrMgLiSiO4F:Eu2+ phosphor.Based on the photoluminescence analysis,Sr2LiSiO4F:Eu2+ phosphor exhibited a green broad emission band of main peak at 513 nm under the excitation of 365 nm,while the Sr2MgSi2O7:Eu2+ and SrMgLiSiO4F:Eu2+ phosphor showed blue emission centered at 467 nm.The temperature dependent photoluminescence properties and room temperature decay time for the three kinds of phosphors were also discussed in this paper.  相似文献   

4.
Novel red-emitting Eu3+, Sm3+ singly doped and co-doped Ca14Mg2(SiO4)8 phosphors were prepared by conventional solid- state reaction. Powder X-ray diffraction patterns were employed to confirm phase pu...  相似文献   

5.
Eu3+activated Ca4Y6(SiO4)6O phosphors were prepared by combustion synthesis method, and their morphologies and lu-minescent properties were investigated. Field scanning electron microscopy (FSEM) confi...  相似文献   

6.
The luminescent properties of Eu3 doped Ca2SiO4 red phosphors synthesized by the flux fusion reaction method were investigated. It was found that the excitation spectrum included two regions: the weak excitation band below 325 nm and strong narrow peaks above 325 nm. The main peak of the excitation band was located at 400 nm. The peaks located at 290 nm were assigned to the combination of the charge transfer transition of O-Eu, peaks above 325 nm (325, 385, 400, 470, 511, and 539 nm) were assigned to the f–f transitions of Eu3 . The emission spectrum was dominated by the red peak located at 612 nm due to the electric dipole transition of 5D0–7F2. In addition, the ef- fects of the Eu3 content and charge compensators of Li , Na , K , and Cl– ions on the emission intensity were investigated. The experiment results suggested that the strongest emission was obtained when the concentration of the Eu3 ions was 0.3 mol–1, and Li ions gave the best improvement to enhance the emission intensity. Ca2SiO4:Eu3 , Li was thus suitable for low-cost trichromatic white light emitting diodes (WLED) based on UV InGaN chip.  相似文献   

7.
Eu2+ and (or) Eu3+ doped Sr2SiO4 phosphors particles were synthesized by a conventional solid-state reaction technique, and their structural and optical properties were investigated. The X-ray diffraction (XRD) results showed that the obtained phosphors were composed of orthorhombic α'-Sr2SiO4 and monoclinic β-Sr2SiO4 phase. When excited under 256 nm, Sr2SiO4:Eu3+ phosphors showed intense emission in the red region. Sr2SiO4:Eu3+ phosphors exhibited white emissions (x=0.30, y=0.40, TC=6500 K) ranging from 425 to 650 nm when it was excited by near-ultraviolet (near-UV) light, indicating that Sr2SiO4:Eu2+ was a good light-conversion phosphor candidate for near-UV chip.  相似文献   

8.
9.
A series of blue long afterglow mixed halide-phosphate phosphors Sr5 (PO4)3 FxCl1-x:Eu2+,Gd3+were synthesized in air by traditional solid-state reaction route. The crystal structures, photoluminescence...  相似文献   

10.
Ca8Mg(SiO4)4Cl2:Eu2 phosphor doped with Sr2 cation for Ca2 partially, was synthesized by solid-state reaction at high temperature under reducing atmosphere, and its luminescent properties were investigated. The experimental results indicate that the emission intensity of the phosphor increases after being doped with a few amount of Sr2 ion. The emission peak of the phosphor blue shift to about 464 nm when the phosphor is doped with large quantity of Sr2 ions. The excitation spectrum indicates that the phosphor can be well excited by UV and blue light from 300 to 460 nm, and the phosphor was fitted well for the excitation by UV or blue-LED.  相似文献   

11.
12.
A flower-like Eu2+ and Dy3+ co-doped SrAl2O4 long-lasting phosphorescent (LLP) phosphor was synthesized via the inorganic- salt-based sol-gel method.The crystal structure,morphology and optical properties of the composite were characterized.X-ray diffraction diffu-sion (XRD) data and DSC-TG curves of the phosphor revealed that the SrAl2O4 crystallites have been formed after the precursor was calcined at 900 °C and to be single-phase SrAl2O4 at 1100 °C.The SEM photographs indicated that the sample exhibited ...  相似文献   

13.
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 Eu<3+ ions in YAl3(BO3)4: Eu3+ phosphors was 8 mol%.  相似文献   

14.
La0.75NbO4:Eu3+0.25 and La0.65NbO4:Eu3+0.25,Bi3+0.10 phosphors were synthesized by solid-state reaction method,and their photoluminescence properties were discussed in detail.With the increased incorporation of the co-activator Bi3+,the charge transfer(CT) bands of Nb5+→O2-and Eu3+→O2-(-280 nm) weakened and a new and significant broad band Bi3+-O2-(-330 nm) appeared,while the peaks at 395 and 466 nm assigned to f-f transitions of Eu3+ was slightly changed.Compared with the commercial phosphor Y2O2S:0.05Eu3+...  相似文献   

15.
LiCaBO3:Eu3+ phosphor was synthesized by high solid-state reaction method, and its luminescent characteristics were investigated. The emission and excitation spectra of LiCaBO3:Eu3+ phosphors exhibited that the phosphors could be effectively excited by near ultraviolet (400 nm) and blue (470 nm) light, and emitted red light. The effect of Eu3+ concentration on the emission spectrum of LiCaBO3:Eu3+ phos-phor was studied. The results showed that the emission intensity increased with increasing Eu3~ concentration, and then decreased because of concentration quenching. It reached the maximum at 3mol.% Eu3+, and the concentration self-quenching mechanism was the d-d interaction according to the Dexter theory. Under the conditions of charge compensator Li+, Na+ or K+ incorporated in LiCaBO3, the emission intensities of LiCaBO3:Eu3+ phosphor were enhanced.  相似文献   

16.
以三氧化二铕和正硅酸乙酯为原材料,利用溶胶-凝胶法、高温机械力化学法合成了SiO_2∶Eu~(3+)粉体.用X射线衍射(XRD)、扫描电镜(SEM)表征了材料的结构和形貌,采用激发光谱、发射光谱对荧光粉体的发光性能进行了测量.结果说明:溶胶-凝胶法、高温机械力化学法合成样品的发光性能随着热处理温度的增加先增强后减弱,分别在900℃和600℃达到最好,粉体平均粒度分别为2μm与1μm.与溶胶-凝胶法比较,高温机械力化学法的制备温度降低了300℃.且利用高温机械力化学法制备的样品的发光性能要好于溶胶-凝胶法制备的样品.  相似文献   

17.
The europium-doped LaF3 nanoparticles were prepared by refluxing method in glycerol/water mixture and characterized with X-ray diffraction(XRD), field emission scanning electron microscopy(FE-SEM), UV-vis diffuse reflectance spectrum, and photoluminescence spectra. The results of XRD indicated that the obtained LaF3: Eu3+ nanoparticles were well crystallized with a hexagonal structure. The FE-SEM image illustrated that the LaF3: Eu3+ nanoparticles were spherical with an average size around 30 nm. Under irradiation of UV light, the emission spectrum of LaF3: Eu3+ nanoparticles exhibited the characteristic line emissions arising from the 5D0→7FJ (J=1, 2, 3, 4) transitions of the Eu3+ ions, with the dominating emission centered at 590 nm. In addition, the emissions from the 5D1 level could be clearly observed due to the low phonon energies (-350 cm-1) of LaF3 matrix. The optimum doping concentration for LaF3: Eu3+ nanoparticles was determined to be 20mol.%.  相似文献   

18.
Novel red-emitting phosphors Sr2MgSi2O7:Eu3+ were prepared by gel-combustion method assisted by microwave. The phase struc-ture and luminescent properties of as-synthesized phosphors were investigated by XRD and fluorescence spectrophotometer, respectively. The results showed that the as-synthesized sample was Sr2MgSi2O7 with tetragonal crystal structure. The excitation spectrum of Sr2MgSi2O7:Eu3+ was composed of two major parts: one was the broad band between 200 and 350 nm, which belonged to the charge transfer of Eu3+-O2-; the other consisted of a series of sharp lines between 350 and 450 nm, ascribed to the f-f transition of Eu3+. The emission spec-trum consisted of two emission peaks at 593 and 616 nm, which was attributed to 5D0→7F1 and 5D0→7F2 of Eu3+, respectively. The concen-tration of Eu3+ (x) had great effect on the emission intensity of Sr2-xMgSi2O7:Eu3+x. When x varied in the range of 0.04-0.18, the intensity of emission peaks at 593 and 616 nm increased gradually with the concentration of Eu3+ increasing. It was interesting that no concentration quenching occurred. Moreover, the luminescent intensity could be greatly enhanced with incorporation of charge compensator Li+ ions.  相似文献   

19.
Eu3+ -activated Gd2(MoO4)3 pseudo-pompon-like red-emitting phosphors were prepared by solid-state method.The structure,morphology,and luminescent properties of these powder samples were investigated by X-ray diffraction (XRD),scanning electron microscopy(SEM),and fluorescent spectrophotometry,respectively.The as-obtained phosphors were single crystalline phase with orthorhombic unit cell.The particles of the powder samples had the length of 5-12 μm and width of 3-7 μm with flake shape and large surface area,which is suitable for manufacture of white LEDs.The phosphor could be efficiently excited by the incident light of 348-425 nm,well matched with the output wavelength of near-UV (In,Ga)N chip,and re-emitted an intense red light peaking at 615 nm.By combing this phosphor with a~395 nmemitting (In,Ga)N chip,a red LED was fabricated,so that the applicability of this novel phosphor to white LEDs was confirmed.It is considered to be an efficient red-emitting conversion phosphor for solid-state lighting based on (In,Ga)N LEDs.  相似文献   

20.
The blue-emitting phosphor NaBaPO4:Eu2+ was prepared by the combustion method. The phase structure and microstructure of the as-prepared samples were characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM), respectively. Under the excita-tion wavelength of 360 nm, the emission spectrum exhibited only one blue band centering at 435 nm, which was ascribed to the 4f65d1→4f7 transition on Eu2+ ions. Compared with the phosphor obtained by solid-state reaction method, the relative emission intensity of sample ob-tained by combustion method increased slightly. The decay times and the temperature dependence luminescence intensities (25-300 oC) were discussed in order to further investigate the potential applications. Furthermore, Eu2+-doped NaBaPO4 phosphor showed higher thermally sta-ble luminescence comparable to commercially available Y3Al5O12:Ce3+ (YAG:Ce3+) phosphor. All the investigated suggestions that Na-BaPO4:Eu2+ is a good phosphor candidate applied in white light emitting diode.  相似文献   

设为首页 | 免责声明 | 关于勤云 | 加入收藏

Copyright©北京勤云科技发展有限公司  京ICP备09084417号