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1.
The photoluminescence properties of BiTaO4∶Pr3+ and BiTaO4 at room temperature were studied, and the infrared transmission and diffusion reflection spectra of BiTaO4 were measured. The photoluminescence spectrum of BiTaO4 peaks at about 420, 440 and 465 nm. There has an obvious excitation band from 330 to 370 nm. The photoluminescence spectrum of BiTaO4∶Pr3+ consists of the characteristic emission of Pr3+, and its main peak is at 606 nm from 3P0→3H6 transition of Pr3+. Its excitation spectrum consists of the wide band with maximum at 325 nm, the wide band in the range of 375~430 nm, and the characteristic excitation of Pr3+. The bands at 325 nm and 375~430 nm may be from the absorption of the charge transfer transition of the tantalate group and defect energy levels in its forbidden band, respectively. There is energy transfer from host to Pr3+. Because both the host density and photoluminescence peak intensity of BiTaO4∶Pr3+ are superior to PbWO4, BiTaO4∶Pr3+ may be a potential heavy scintillator. 相似文献
2.
The luminescent properties of Eu^3+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 Eu^3+. 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 effects of the Eu^3+ 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 Eu^3+ ions was 0.3 mol^-1, and Li^+ ions gave the best improvement to enhance the emission intensity. Ca2SiO4:Eu^3+, Li^+ was thus suitable for low-cost trichromatic white light emitting diodes (WLED) based on UV InGaN chip. 相似文献
3.
Luminescent properties of Ca2SiO4:Eu3+ red phosphor for trichromatic white light emitting diodes 总被引:3,自引:0,他引:3
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
4.
SrGdGa3O7:RE(RE=Ce^3 ,Pr^3 ,Tb^3 ) were prepared by traditional solid-state reaction and their luminescence properties in the range of VUV-Vis were investigated. The two broad bands situated at about 177 and 217nm in excitation spectra are attributed to the host lattices absorption, and they have no considerable change when doped different rare earth ions. The f-d transitions of Pr^3 and Tb^3 calculated by the formula gathered by Dorenbos were compared to the experimental results. The excitation spectra also show the sharp Gd^3 excitation line at about 274 nm pointing to an efficient energy transfer from Gd^3 to Pr^3 and Tb^3 . All of the emission spectra present the characteristic emissions of rare earth ions when excited by VUV and UV. 相似文献
5.
Excitation and emission spectra of new borate La2CaB10O19 doped Eu^3 in VUV-VIS range, high resolution emission spectra at room temperature and lifetime of Eu^3 were investigated. The emission line at about 616nm attributed to the ^5D0-^7F2 transition of Eu^3 is the most intense emission of Eu^3 . The broad band at about 244nm is originated from charge transition band (CTB) of O^2→Eu^3 . According to the numbers of spectral lines ^5D0-^7F0 and ^5D0-7F1 in highresolution spectrum, Eu^3 ions occupy two crystallographic sites. The lifetimes of ^5D0-^7F0 transition of Eu^3 of two kinds of lattice sites are individually 2.1 and 2.6ms, and both are exponential decay. In the VUV excitation spectrum, complicated band between 130 and 170nm consists of host absorption and f-d transition of Eu^3 . 相似文献
6.
《中国稀土学报(英文版)》2017,(2)
Samarium doped pyrovanadate Ba_2V_2O_7:Sm~(3+) phosphors were synthesized by traditional high-temperature solid-state reaction method. The phase and the structure of the samples were characterized by powder X-ray diffraction(XRD), and the luminescent properties and the energy transfer mechanism of the material were investigated using quantitative photoluminescence(PL) spectroscopy. The excitation spectrum of the sample exhibited a broad ultraviolet(UV) band with maximum at around 341 nm due to V–O charge transfer transition of the host. The emission spectrum displayed a yellow-greenish broadband(peaking at around 498 nm) coming from the host Ba_2V_2O_7 and three narrow peaks(at 561, 599 and 646 nm) attributed to the dopant Sm~(3+) ions. The PL spectra revealed the energy transfer from the host to the Sm~(3+) ions. In addition, the color coordinates and the color temperature of the phosphor Ba_(1.95)V_2O_7:5%Sm~(3+) were(0.314, 0.365) and 6135 K, respectively, under 365 nm excitation, suggesting it to be a candidate of single-phase converting phosphors for white-light-emitting diodes(WLEDs) with near-UV chips. 相似文献
7.
Anxiang Guan Zuizhi Lu Fangfang Gao Xiaoshan Zhang Huan Wang Tianjiao Huang Liya Zhou 《中国稀土学报(英文版)》2018,36(3):238-242
A series of Eu~(2+),Tb~(3+)-codoped Sr_3 Y(PO_4)_3(SYP) green phosphors were synthesized by hightemperature solid-state reaction. Several techniques, such as X-ray diffraction, UV-vis spectrum,and photoluminescence spectrum, were used to investigate the obtained phosphors. The present study investigates in detail photoluminescence excitation and emission properties, energy transfer between the two dopants, and effects of doping ions on optical band gap. SYP:0.05 Eu2+ phosphor shows an intense and broad excitation band ranging from 220 to 400 nm and exhibits a bright green emission band with CIE chromaticity coordinates(0.189, 0.359) under 350 nm excitation. Green emission of SYP:0.03 Tb3+ is intensified by codoping with Eu~(2+), and energy transfer mechanism between them is demonstrated to be a dipole-dipole interaction. Upon 350 nm excitation, SYP:Eu~(2+),Tb~(3+) phosphors exhibits two dominating bands peaking at 466 and 545 nm, which are assigned to 4 f~65 d~1→4 f~7 transition of Eu~(2+) ions and ~5 D_4→~7 F_5 transition of Tb~(3+) ions, respectively. Optimal doping concentrations of Eu~(2+) and Tb~(3+) in the SYP host are 5 mol% and 15 mol%, respectively. Results indicate that SYP:Eu~(2+),Tb~(3+) phosphors are potentially used as green-emitting phosphors for white light-emitting diodes. 相似文献
8.
A novel red phosphor Ca2GeO4:Eu3+ was prepared by the traditional solid state reaction. X-ray powder diffraction (XRD) analysis suggested that there was no impurity phase. The study on the diffusion reflection spectra of the undoped and Eu3+ doped Ca2GeO4 phosphors revealed an absorption band superposed of that of the host material and the Eu3+ ions. And the excitation spectrum presented a dominating broad band at 250–300 nm which was attributed to both the host material absorption and the charge transfer band (CTB) of the Eu3+ ions. The investigation on the excitation and diffusion spectra showed that there was an effective energy transfer from the host material to the Eu3+ ions. This was favorable to the red emission of the phosphor. Photoluminescence measurements indicated that the phosphor presents bright red emission at 611 nm under UV excitation. In addition, the Al3+ or Li+ codoping enhanced the red emission from Ca2GeO4:Eu3+ by about 3 and 2 times respectively under UV excitation. 相似文献
9.
The luminescence of EU^2+ in BaMgSiO4 with BaB2O4 as flux was studied. The emission spectrum of the phosphor consisted of two bands, peaking at about 398 nm and 515 nm, which were attributed to the emissions from different Eu^2+ sites in the lattice. When the BaB2O4 flux was applied, the intensity of the 398 nm emission was not clearly affected, but the intensity of the 515 nm emission was enhanced by about ten times. Gaussian fitting showed that the emission band at around 515 nm could actually be resolved into two bands with peak wavelengths of 499 nm and 521 nm, respectively. The assignments of the emission bands to the cation sites were carried out according to the values of bond valence. The overlapping of the 398 nm emission band on the excitation band of 515 nm emission implied that energy transfer could occur from the luminescent center related to the 398 nm emission to the center related to the 515 nm emission, and the energy transfer process remarkably enhanced the intensity of the 515 nm emission band. The phosphor had strong excitation at around 350-400 nm and emitted a bright green luminescence. Thus it could have applications as a green component in solid-state lighting devices assembled by near-UV Light Emitting Diodes (LED) combined with tricolor phosphors. 相似文献
10.
Synthesis and Luminescent Properties of Superfine Sr2CeO4 Phosphors by Sol-Gel Auto- Combustion Method 总被引:2,自引:0,他引:2
Citric acid complexing sol-gel auto-combustion method was explored to synthesize superfine Sr2CeO4 phosphors using the inorganic salts Sr(NO3)2 and Ce(NO3)3 as raw materials together with citric acid (CA) as a chelating agent. TGDTA, XRD, SEM and photoluminescence spectra were used to investigate the formation process, microstructure and luminescent properties of the synthesized Sr2CeO4. The results show that the crystallization of Sr2CeO4 begins at about 800 ℃ and completes around 900 ℃ with an orthorhombic structure. When the calcination temperature is above 1000 ℃, Sr2CeO4 partly decomposes into SrCeO3. SEM studies show that the particles of Sr2CeO4 obtained at 900 ℃ are sphericallike shape and superfine with diameter below 100 nm. The excitation spectrum of the superfine Sr2CeO4 phosphors displays a broad band with two peaks around 290 and 350 nm respectively. The former peak is stronger than the latter one. This broad band is due to the charge transfer (CT) band of the Ce^4+ ion. Excited by a radiation of 290 nm, the superfine phosphors emit a strong blue-white fluorescence, and the emission spectrum shows a broad band with a peak around 470 nm, which can be assigned to the f→t1g transition of Ce^4+ . It is found that the emission intensity is affected by the calcination temperature. 相似文献
11.
Calcium magnesium chlorosilicate doped by europium, Ca8Mg(SiO4)4Cl2: Eu^2+, was prepared by the solid state reaction at high temperature. The compound obtained is pure Ca8Mg(SiO4)4Cl2 phase with cubic structure. Its average particle size is 5 μm, and it has good dispersity and morphological form. The excitation spectrum of Ca8Mg(SiO4)4Cl2: Eu^2+ is a wide band, which covers from 270 to 480 nm. The emission spectrum is also a wide band peaked at 510 nm. The luminescent intensity reaches to the maximum when the concentration of Eu^2 + is 2%. The wavelength of emission and excitation of the phosphor with various Eu^2 + contents keeps constant. This spectrum range matches violet and blue LED chips very well, and its strong luminescence intensity is suitable for a green phosphor of tricolor phosphor of white light LED. 相似文献
12.
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... 相似文献
13.
Photoluminescence of BaGdB9O(16):Eu^3+ co-doped Al^3+ or Sc^3+ under UV-VUV excitation 总被引:1,自引:1,他引:0
Single phase of BaGd0.9-xMxEu0.1B9O16 (M=Al or Sc, 0≤x≤0.3) powder was prepared by the solid-state reaction and its photoluminescence (PL) properties were investigated under ultraviolet (UV) and vacuum ultraviolet (VUV) excitation. Monitored with 613 nm emission, the excitation spectra of BaGd0.9-xMxEu0.1B9O16 consisted of three broad bands peaking at about 242, 208, and 142 nm, respectively. The one at about 242 nm originated from the charge transfer band (CTB) of O2-→Eu3+. The other two were assigned to the absorption of the host, which was overlapped with absorptions among borate groups, f→d transition of RE3+ (RE=Gd, Eu), and the charge transfer transition of O2-→Gd3+. The maximum emission peak was observed at about 613 nm in the emission spectra of BaGd0.9-xMxEu0.1B9O16 under both 254 and 147 nm excitation, which originated from the electric dipole 5D0→7F2 transition of Eu3+. When excited with 254 nm, the integral emission intensity of Eu3+ increased after Al3+ or Sc3+ substituting Gd3+ partly in BaGd0.9Eu0.1B9O16. Under 147 nm excitation, the integral emission intensity of Eu3+ decreased after some Gd3+ was replaced by Sc3+, but increased after adding appropriate Al3+ into BaGd0.9Eu0.1B9O16. 相似文献
14.
A barium-phosphate glass matrix was co-doped with Sn O and Eu2O3 for investigating on material luminescent properties. Optical absorption and X-ray photoelectron spectroscopy(XPS) were employed in the characterization of tin species. The prevalence of divalent tin was indicated by the XPS data in accord with a conspicuous absorption band detected around 285 nm ascribed to twofold-coordinated Sn centers(isoelectronic with Sn2+). Photoluminescence(PL) excitation spectra obtained by monitoring Eu3+ emission from the 5D0 state revealed a broad excitation band from about 250 to 340 nm, characteristic of donor/acceptor energy transfer. Under excitation of such at 290 nm, the co-doped material exhibited a bright whitish luminescence, and a four-fold enhanced Eu3+ emission relative to a purely Eu-doped reference. Time-resolved PL spectra recorded under the excitation at 290 nm exposed a broad band characteristic of the twofold-coordinated Sn centers and emission bands of Eu3+ ions, which appeared well separated in time in accord with their emission decay dynamics. The data suggested that light absorption took place at the Sn centers(donors) followed by energy transfer to Eu3+ ions(acceptors) which resulted in populating the 5D0 emitting state. Energy transfer pathways likely resulting in the enhanced Eu3+ photoluminescence and the consequential light emission were discussed. 相似文献
15.
The single phase of BaGd1-xTbxB9O16(0.05≤x≤0.3) was prepared by the solid-state reaction.Their photoluminescence properties were investigated under vacuum ultraviolet(VUV) excitation.Monitored by 541 nm emission,the excitation spectrum of BaGd0.75Tb0.25B9O16 consisted of one broad band centered at about 148 nm and some bands in 163 to 282 nm.The former was assigned to the overlapped absorptions among borate groups,charge transfer bands(CTBs) of O2-→Ln3+(Ln=Tb,Gd) and the f→d transition of Gd3+.The bands in ... 相似文献
16.
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. 相似文献
17.
田莲花 《中国稀土学报(英文版)》2010,28(1):37-39
The photoluminescence(PL) properties of Ca4YO(BO3)3 doped with Bi3+,Dy3+,and Pr3+ ions were investigated.These compounds were prepared using a typical solid-state reaction.The excitation and emission spectra were measured using a spectrofluorometer.For Ca4YO(BO3)3:Bi3+,the excitation spectrum showed the bands at about 228,309,and 370 nm which correspond to the 1S0→1P1 transition and the 1S0→3P1 transition of Bi3+ ions.The emission band at 390 nm corresponded to the 3P1→1S0 transition of Bi3+ ions.For Ca4YO(BO3)3:Bi3+,Dy3+,energy transfer occurred from Bi3+ to Dy3+ somewhat.In Ca4YO(BO3)3:Bi3+,Dy3+,Pr3+,the excitation band at 367 nm was enhanced obviously due to the energy migration from Bi3+ to Pr3+,which converted efficiently the emission of semiconductor InGaN based light-emitting diode(LED).Therefore,the emission of Dy3+ ions was enhanced due to the energy migration from the process of Bi3+→Pr3+→Dy3+.It resulted in the good color rendering. 相似文献
18.
(Y, Gd)Al3 (BO3)4:Eu^3 samples were prepared by the conventional solid state reaction. The XRD results indicate that the crystal symmetry is low. The excitation spectrum is composed of two broad bands centered at about 170 and 250 nm respectively. In the emission spectra, the peak wavelength is about 616 nm under 147 nm VUV excitation. The luminescent chromaticity coordinate and the relative intensity change along with Gd^3 mole concentration in the range of 0.15 to 0.85 mol (and Eu^3 mole concentration, 0.02 to 0. 1 mol). The correlative data show that the concentration quenching occurs when the Eu^3 mole concentration ranges from 0.02 to 0.1 mol, and the Gd^3 →Gd^3 , Gd^3 →Eu^3 and host→Eu^3 , Gd^3 energy transfers exist, and Gd^3 mole concentration influences Eu^3 emission. 相似文献
19.
Divalent europium activated tristrontium dialuminum hexaoxide phosphor, (Sr1-xEux)3Al2O6, was obtained by solid state reaction. Crystal structure and luminescence properties of synthesized (Sr1-xEux)3Al2O6 were investigated. The major excitation band of (Sr1-xEux)3Al2O6 located in blue light region, the photoluminescence spectrum showed red light emission peaked at 618 nm which could be attributed to the d-f transition of the Eu2+. The influence of Ca2+ substitution for Sr2+ on structural and luminescence properties of Eu2+ doped Sr3Al2O6 was also studied. The photoluminescence peak position of (Sr1-yCay)2.94Eu0.06Al2O6 varied from 618 to 655 nm with increasing y value. The reason for redshift in the emission band of (Sr1-yCay)2.94Eu0.06Al2O6 phosphor was also discussed. 相似文献
20.
《中国稀土学报(英文版)》2017,(9)
A series of tunable phosphors NaAlSiO_4:Ce~(3+),Sm~(3+) were synthesized using a conventional high-temperature, solid-state method. Crystal structure, photoluminescence excitation, and emission spectra with fluorescence decay curves were investigated. Under UV excitation(325 nm), NaAlSiO_4:Ce~(3+),Sm~(3+) showed strong blue emission located at 444 nm and orange-reddish emission centered at 563, 601, 648 and 712 nm, stemming from the characteristic emission for 4f-5d transition of Ce~(3+) and ~4G_(5/2)→~6H_J(J=5/2, 7/2, 9/2, 11/2) transition of Sm~(3+), respectively. In addition, we studied the detailed energy transfer process between Ce~(3+) and Sm~(3+) and found that it belonged to dipole-dipole resonance energy transfer. Furthermore, we noted that the white light emitting from the Ce~(3+), Sm~(3+) co-doped phosphors with the color coordinate(x=0.313, y=0.283) could be observed under 325 nm excitation, which was close to the ideal white light(x=0.33, y=0.33). The results indicated that this phosphor has a potential application as a single-phased alumino-silicate phosphor for ultraviolet white light-emitting diodes(UV-WLEDs). 相似文献