271 resultados para CEF3-TB3


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-Ca2RSSiO46O2RYGdYVO4LaPO41Eu3+Tb3+Dy3+Sm3+Er3+Pb2SEMAFMCa2R8SiO46O2RYGdEu3+Tb3+Ca2Y8SiO46O26hCs4fC35Do-7F25D4-7F5Eu3+Tb3+Y3+10mol6molCa2Y851O46O2:Eu3Ca2Y8SiO46O2:Tb3+800Pb2Ca2Gd8SiO4 6O2Gd3+Pb2Gd3Gd3nA3YVO4PechiniYvO4:AAEu3 Dy3Sm3Er3YVO4VO43-Dy3Sm3Er3Y3+2molLaPO4Etl3+591nm5Do-7FlTb3543nm5D4-7F5Ce35d-4fTb3Eu3+Tb3+Eu3+Tb3LaPO4:CeTbCe3+Tb3+95XRDx0x1 YVxP1-xO4:Eu3+YVxP1-xO4:Eu3+0x1xEu3+x0Eu3+1Eu3+5Do7F2Etlsx0Y0.98Eu0.l2PO4Eu3+D2d5D07FISD07F2xY0.98Eu0.02VxP1-xO40xl0x0.5Eu3+5 D0-7F2x0.6Eu3+5D0-7F2YVxP1-xO4:A30x1AErSmVO43-A3+VO43-VO43-n-A3+n1VO43-0.1x1xx1VO43-A3+xRVO4:A3+RYLaGdAEuSmErRA3+YVO4GdVO4D2dYVO4GdVO4A3+LaVO4A3+LaVO4C1C1D2dA3+Gd3+A3+GdVO4

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AAO5200nmAAOAAOAAOM2O3:RE3+MY,Gd; REEuTbAAOAAO15Onm35nm2OnmAAOAAO2XRD331AAOAAO-Al2O33AAO350600nm435nm4AAOYO.96RE0.05O3REEuTbSEMEDXTEMSAEDXRDPLx-XRDSAEDRE2O3REYGdEu3D07F2Tb35D47FJJ=65435M2O3:RE3MYGdREEuTbAAO6M2O3:RE3M=YGdREEuTbO7YGd2O3:Eu3+AAOAAO 8M2O3: RE3+MYGdREEuTb0AAO

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4fN-1n'l'4fN-1n'l'6604fN-1n'l'n'l'=5d6s6p4fN-1n'l'fN-15d4fN-15dfdhe[fciaiQi2]1/2Dy3+Tb3+fCe3+Eu2+4fN-15dheheCe3+Ey2+4fN-15dCe3+Eu2+4fN-15dFcEhQfi/NFc10Dq4fN-15dCe3+Eu2+heFc4fN-1n'l

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MB4O7:REM=Sr BaREDTbTm HoZn4B6O13REREDy,TbTmHo ZnBO22:REREDy,TbTmHoM3PO42:REM=SrBaREDu, TbRD60Cop- MB407DyM=SrBaZn4B6O13:DyZnBO22DyZnoTb Sr3PO42:DyMB4O7:DyM=SrB EPR 60Cop- D3+Tb3+ 60Cop 760Cox p-p-

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Silica-based functionalized terbium fluorescent nanoparticles were prepared, characterized and developed as a fluorescence probe for antibody labeling and time-resolved fluoroimmunoassay. The nanoparticles were prepared in a water-in-oil (W/O) microemulsion containing a strongly fluorescent Tb3+ chelate. N,N.N-1,N-1-12,6-bis(3'-aminomethyl-1'-pyrazolyl)phenylpyridine] tetrakis(acetate)-Tb3+ (BPTA-Tb3+), Triton X-100, octanol, and cyclohexane by controlling copolymerization of tetraethyl orthosilicate (TEOS) and 3-[2-(2- aminoethylamino)-ethylamino]propyl-trimethoxysilane (AEPS) with ammonia water. The characterizations by transmission electron microscopy and fluorometric quantum methods show that the nanoparticles are spherical and uniform in size, 45 +/- 3 nm in diameter, strongly fluorescent with fluorescence yield of 10% and a long fluorescence lifetime of 2.0 ms. The amino groups directly introduced to the nanoparticle's surface by using AEPS in the preparation made the surface modification and bioconjugation of the nanoparticles easier. The nanoparticle-labeled anti-human alpha-fetoprotein antibody was prepared and used for time-resolved fluoroimmunoassay of (x-fetoprotein (AFP) in human serum samples. The assay response is linear from 0.10 ng ml(-1) to about 100 ng ml(-1) with the detection limit of 0.10 ng ml(-1). The coefficient variations (CVs) of the method are less than 9.0%. and the recoveries are in the range of 84-98% for human serum sample measurements. (C) 2004 Elsevier B.V. All rights reserved.

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Nanocrystalline Tm3+-doped La2O3 phosphors were prepared through a Pechini-type sol-gel process. X-ray diffraction, field-emission scanning electron microscopy, photoluminescence, and cathodoluminescence spectra were utilized to characterize the synthesized phosphors. Under the excitation of UV light (234 nm) and low-voltage electron beams (1-3 kV), the Tm3+-doped La2O3 phosphors show the characteristic emissions of Tm3+(D-1(2), (1)G(4)-F-3(4), H-3(6) transitions).

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In this paper, we present a facile and general synthetic route to high-quality alkaline earth metal fluoride (AEF(2), AE = Ca, Sr, Ba) nanocrystals and CaF2:Tb3+ nanocrystals based on the thermal decomposition of corresponding trifluoroacetate precursors in hot oleylamine. X-ray diffraction, transmission electron microscopy, thermogravimetric and differential thermal analysis, Fourier transform infrared spectra, photoluminescence spectra, and kinetic decays were employed to characterize the samples. The use of single-source precursors plays an important role in the formation of high-quality AEF(2) nanocrystals, and the formation process is demonstrated in detail.

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Tb(1-x)BO3:xEu(3+) (x = 0-1) microsphere phosphors have been successfully prepared by a simple hydrothermal process directly without further sintering treatment. X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), thermogravimetric analysis (TGA), scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution transmission electron microscopy (HRTEM), selected area electron diffraction (SAED), photoluminescence (PL), low-voltage cathodoluminescence (CL), and time-resolved emission spectra as well as lifetimes were used to characterize the samples.

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Lu3Ga5O12:Eu3+, Lu3Ga5O12:Tb3+, and Lu3Ga5O12:Pr3+ phosphors were prepared through a Pechini-type sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), photoluminescence, and cathodoluminescence spectra were utilized to characterize the synthesized phosphors. The XRD results reveal that the sample begins to crystallize at 800 degrees C and fully crystallined pure Lu3Ga5O12 phase can be obtained at 1000 degrees C. The FESEM image indicates that the phosphor sample is composed of aggregated rice grainlike particles with sizes around 80-120 nm.

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LiCaBO3 was synthesized by high-temperature solid-state reaction. The influence of different rare earth dopants, i.e. Dy3+, Tb3+. TM3+ and Ce3+, on thermoluminescence (TL) of LiCaBO3 phosphor was discussed. We studied the TL properties and some dosimetric characteristics of Ce3+-activated LiCaBO3 phosphor in detail. The effect of the concentration of Ce3+ on TL was investigated, the result of which showed that the optimum Ce3+ concentration was 1 mol%. The TL kinetic parameters of LiCaBO3:0.01 Ce3+ were studied by computer glow curve deconvolution (CGCD) method.

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Cyanex 923CeF3,CeF3CeF3CeF3,CeF3255 nm;;,TiO2CeF3,250~400 nmTiO2CeF3,

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Uniform rare earth phosphate (REPO4, RE = La-Tb) nanocrystals were successfully synthesized in a properly designed TBP/[Omim]Cl/H2O (tributylphosphate/1-octyl-3-methyl-imidazolium chloride/water) microemulsion system. The phosphoryl groups anchored the TBP molecules oil the surfaces of the nanocrystals, and this made the nanocrystals easily dispersed in some imidazolium-based ILs. LaPO4:Eu3+ and CePO4:Tb3+ nanocrystals capped with TBP showed bright red and green emission under UV excitation, with enhanced emission intensity and lifetimes compared with the uncapped ones.

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Lanthanum phosphate (LaPO4) nanostructures with different morphologies were prepared by a facile solution-precipitation process. The effect of different reaction conditions on the morphology of nanostructures was studied. When the molar ratio of La3+:H3PO4 was around 1 : 2, 1 : 20, 1 : 100, and 1 : 200, four different morphologies, such as near-spherical, snowflake-like, star-shaped, lens-like nanostructures and short nanorods, were obtained, respectively. Meanwhile, similar shapes developed when the molar ratio of H3PO4 to ionic surfactants, such as SDS and CTAB, was varied. In addition, Eu3+ doped and Ce3+/Tb3+ co-doped LaPO4 nanostructures showed morphology evolution similar to undoped LaPO4 nanostructures. The optical properties of these doped LaPO4 were also characterized.

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LaAlO3:Tm3+ and LaAlO3:Tb3+ phosphors were prepared through a Pechini-type sol-gel process. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), photoluminescence, and cathodoluminescence (CL) spectra were utilized to characterize the synthesized phosphors. The XRD results reveal that the fully crystalline pure LaAlO3 Phase can be obtained at 800 degrees C. The FE-SEM image indicates that the phosphor samples are composed of aggregated spherical particles with sizes ranging from 40 to 80 nm. Under the excitation of ultraviolet light (230 nm) and low-voltage electron beams (1-3 kV), the LaAlO3:Tm3+ and LaAlO3:Tb3+ phosphors show the characteristic emissions of Tb3+ (D-1(2)-> H-3(6,4),F-3(4) transitions) and Tm3+ (D-5(3,4)-> F-7(6,5,4,3) transitions) respectively. The CL of the LaAlO3:Tm3+ phosphors have high color purity and comparable intensity to the Y2SiO5:Ce3+ commercial product, and the CL colors of Tb3+-doped LaAlO3 phosphors can be tuned from blue to green by changing the doping concentration of Tb3+ to some extent.

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Spherical SiO2 particles have been coated with rare earth oxide layers by a Pechini sol-gel process, leading to the formation of core-shell structured SiO2@RE2O3 (RE = rare earth elements) and SiO2@Gd2O3:Ln(3+) (Ln = Eu, Tb, Dy, Sm, Er, Ho) particles. X-ray diffraction (XRD), field emission scanning electron microscopy (FE-SEM), transmission electron microscopy (TEM), photoluminescence (PL), and cathodoluminescence spectra as well as lifetimes were used to characterize the resulting SiO2@RE2O3 (RE = rare earth elements) and SiO2@Gd2O3:Ln(3+) (Eu3+, Tb3+, Dy3+, Sm3+, Er3+, Ho3+) samples. The obtained core-shell phosphors have perfect spherical shape with narrow size distribution (average size ca. 380 nm), smooth surface and non-agglomeration. The thickness of shells could be easily controlled by changing the number of deposition cycles (40 nm for two deposition cycles).