La~(3+) doped LiCo_(0.25)Zn_(0.25)Fe_2O_4 spinel ferrite nanocrystals:Insights on structural,optical and magnetic properties

This paper addresses the manipulation of structural,morphology,optical and magnetic properties of LiCo_(0.25)Zn_(0.25)Fe_2 O_4 ferrite via incorporation of different proportions of La~(3+) at the expense of iron ions using a sol-gel method.The samples were characterized using the X-ray diffraction technique(XRD),Fourier transform infrared(FT-IR) spectroscopy,the energy dispersive X-ray spectra(EDX),inductively coupled plasma optical emission spectroscopy(ICP-OES),high resolution scanning electron microscopy(SEM),Brunauer-Emmett-Teller(BET) surface area analysis,ultraviolet-diffuse reflectance spectroscopy(UV-DRS),and vibrating sample magnetometer(VSM) technique.The Rietveld refinements of the samples indicate that at higher concentrations of La3+,nanostructures with dual phase,i.e.cubic spinel and orthorhombic LaFeO_3 perovskite with space group(Pbnm) appear.Optical studies show that the energy band gap(E_g) of the bare LiCo_(0.25)Zn_(0.25)Fe_2 O_4 ferrite sample(2.18 eV) reaches up to 2.47 eV at x=0.06 and above this concentration,it drops sharply to 2.00 eV.Although the saturation magnetization and the coercivity of LiCo_(0.25)Zn_(0.25)La_xFe_(2-x)O_4 are lower than that of LiCo_(0.25)Zn_(0.25)Fe_2 O_4 NPs.Overall,the superparamagnetic nature and low values of saturation magnetization and coercivity of LiCo_(0.25)Zn_(0.25)La_xFe_(2-x)O_4 NPs are suitable to be applied in transformers core.     

Eco-friendly green synthesis of novel magnetic Fe_3O_4/SiO_2/ZnO-Pr_6O_(11) nanocomposites for photocatalytic degradation of organic pollutant

This study reports the successful so nochemical synthesis of novel Fe_3O_4/SiO_2/ZnO-Pr_6O_(11)(Fe/Si/Zn-Pr_6O_(11)) nanocomposites using fructose as a green capping agent.The influence of various parameters containing capping agent,power and time of ultrasound irradiation was investigated to reach optimum morphology and size conditions.The products obtained were characterized by transmission electron microscopy(TEM),UV/Vis diffuse reflectance spectroscopy(DRS),Fourier transform infrared spectra(FT-IR),vibration sample magnetometer(VSM),scanning electron microscopy(SEM),energy dispersive X-ray microanalysis(EDS) and X-ray diffraction(XRD).The Fe_3O_4/SiO_2/ZnO-Pr_6O_(11) nanocomposites display remarkably enhanced photocatalytic activity towards rhodamine b degradation(89.6%)and Congo red(84.7%) under UV irradiation compared with the other products.The results illustrate that the photocatalytic efficiency of magnetic nanocomposites is very much higher than pure Pr_6O_(11)nanostructures.Magnetic photocatalyst still has good stability after five successive runs.So,these recyclable nanocomposites can play a role in the treatment of both industrial and domestic contaminated water.     

Preparation and luminescence properties of rare-earth doped fiber with spectral blue-shift: SrAl_2O_4:Eu~(2+),Dy~(3+) phosphors/triarylsulfonium hexafluoroantimonate based on polypropylene substrate

The rare-earth doped fiber with spectral blue-shift based on long afterglow luminescent materials SrAl_2O_4:Eu~(2+),Dy~(3+) phosphors and an organic cationic photoinitiators-triarylsulfonium hexafluoroantimonate(TSHF) in the presence of polypropylene substrate(PP) was prepared by melt-spinning process. Scanning electron microscopy(SEM), infrared spectroscopy(IR), afterglow properties and luminescence properties were tested. The results of SEM and FTIR spectra showed that the fiber consisted of irregular particles and had independent structural constitution of SrAl_2O_4:Eu~(2+),Dy~(3+) phosphors, TSHF and polypropylene. Furthermore, it was observed that there existed the highest afterglow initial intensity for the fiber with the TSHF concentration of 5 wt.%. More interestingly, the emission peak shifted to blue area gradually as the TSHF doping increased. The rare-earth doped fiber was distributed on blue light area in the CIE 1931 chromaticity diagram, which showed more obvious blue-shift phenomenon than the yellow-green light of SrAl_2O_4:Eu~(2+),Dy~(3+) phosphors.     

Effect of light conversion agent on luminous properties of a new down-converting material SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent

A new luminous material SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent that can emit red light in the darkness after being excited was fabricated by combining light conversion agent on to SrAl_2O_4:Eu~(2+),Dy~(3+) particles through YsiX3.The morphology of the luminous materials was analyzed by scan electron microscopy(SEM).The emission behavior was evaluated by fluorescence spectrophotometric analysis and the results demonstrated that the emission spectra of samples had a redshift compared to SrAl_2O_4:Eu~(2+),Dy~(3+) and the emission intensity rose dramatically at first and then decreased when the ratio of light conversion agent doping was over 1.4 wt.%.And the emission color of SrAl_2O_4:Eu~(2+),Dy~(3+)/light conversion agent was tuned from green(SrAl_2O_4:Eu~(2+),Dy~(3+))to orange-red.Furthermore,the afterglow property was also investigated,and the results indicated that the afterglow brightness reached 6.5 cd/m~2,and as the light conversion agent concentration increased the brightness intensity decreased.     

原位生成CeB_6颗粒增韧B_4C/Al复合材料的研究

采用无压浸渗法制备了B_4C-CeB_6/Al复合材料, 并对其进行了力学性能测试. B_4C-CeB_6/Al复合材料的密度、抗弯强度、断裂韧性相比单一B4C材料都有很大的提高, 而硬度有所降低. 其抗弯强度值为409.47 Mpa, 比单一碳化硼提高了39.32%; 断裂韧性值6.58 Mpa·m~(1/2), 比单一碳化硼提高了78.80%. B_4C-CeB_6/Al复合材料的抗弯强度和断裂韧性的提高主要有两方面的作用: 一是由于原位生成的CeB_6和B_4C颗粒之间热膨胀系数的不匹配产生残余应力, 从而引起裂纹偏转起到增韧的效果; 二是渗入金属铝的延展性在复合材料中得以体现, 使复合材料韧性增加.     

Effect of RE~(3+) electronegativities on luminescence property of Ba_5Si_8O_(21):Eu~(2+) persistent phosphor

A series of Ba_5Si_8O_(21):0.02Eu~(2+),0.09RE~(3+) persistent phosphors were synthesized by the solid-state reaction method.The measurement results of photoluminescence(PL),phosphorescence and thermoluminescence(TL)were analysed and discussed.The XRD results showed that samples codoped with different RE~(3+) were Ba_5Si_8O_(21) single pure phase.Under the excitation,all samples exhibited a broad Eu~(2+) characteristic emission,and the La~(3+) co-doped sample emitted the brightest photoluminescence even though its persistent luminescence property was the worst because of the weakest electronegativity.However,Nd~(3+) electronegativity was suitable,thus after activation,the Ba_5Si_8O_(21):Eu~(2+),Nd~(3+) sample had the best persistent luminescence performance with the highest phosphorescence intensity and the persistent luminescence decay time beyond 8 h.The Nd~(3+) co-doped sample also had the largest thermoluminescence integral area which proved effectively it had longer persistent luminescence time.The luminescence mechanism was also proposed to study the photoluminescence and persistent luminescence process.These results showed that RE~(3+) electronegativities were distinctly important for persistent phosphors and choosing suitable electronegativity codopant was conducive to enhancing the phosphorescent performance.     

Synthesis and photoluminescent properties of Eu~(3+)/Dy~(3+) doped SrO-Al_2O_3-SiO_2 glass-ceramics

Eu~(3+)/Dy~(3+) single-doped and co-doped 6SrO-3Al_2O_3-91SiO_2 and 12SrO-6Al_2O_3-82SiO_2 glass and glass-ceramics were synthesized successfully by a sol-gel method. The prepared samples were characterized by the X-ray diffraction, high-resolution transmission electron microscopy, photoluminescent spectra and X-ray photoelectron spectroscopy. The effect of annealing temperature, doped ions and matrix component on the structure and the photoluminescent characteristics was systematically studied. The higher temperature was helpful to form nanocrystals and the amount of SrO and Al_2O_3 could better disperse the rare earth ions in matrix at suitable temperature, and both of them could improve the luminescent intensity. Meanwhile, the doped ions could change the luminescent color by single, codoped and energy transfer. The Sr_2SiO_4 nanocrystals were observed in silicates glasses and became larger with the increase of the annealing temperature and the luminous efficiency of rare-earth(RE) ions could be enhanced when the samples changed from glass state to glass-ceramic state. The results indicated that the photoluminescent properties could be changed through controlling the doped ions, annealing temperature and matrix component.     

Mechanism of upconversion emission enhancement in Y_3Al_5O_（12）：Er~（3＋）/Li~＋ powders

Er3+ and Li+ codoped Y3Al5O12(YAG) powders were prepared for a systematic investigation of their upconversion emissions.X-ray diffraction(XRD),upconversion emission spectra,pump power dependence,FT-IR spectra and decay time were studied to characterize the samples.With Li+ doping,the upconversion emission intensity of Er3+ doped YAG powders was obviously enhanced,accompanied with an increase in the ratio of green to red intensity.The enhancement of emission intensity could be attributed to two mechanisms:on...     

Structural characterization and optical properties of long-lasting CaAl_2O_4:Eu~(2+),Nd~(3+) phosphors synthesized by microwave-assisted chemical co-precipitation

The present paper reported the structural and luminescent properties of Eu~(2+) and Nd~(3+) doped CaAl_2O_4 phosphor. The samples were prepared by microwave-assisted chemical co-precipitation(MA-CCP), a synthesis technique which is suitable for small and uniform particle that could be used directly without grinding. The effects of different microwave temperatures on structure and photoluminescence behavior were studied. Formation of a phosphor and phase purity were confirmed by X-ray diffraction technique(XRD) with variable microwave temperatures. XRD analysis showed that the phosphors prepared by MA-CCP method at the temperature of 750, 900oC, respectively and solid-state reaction(SSR) method at 1300oC consisted of impurities. Commission Internationale de L'Eclairage(CIE) color coordinates of CaAl_2O_4:Eu~(2+),Nd~(3+) were suitable as blue light emitting phosphor. Excitation and emission peaks of the samples prepared by different methods in this study were almost the same. The images of SEM showed that the size of the phosphors prepared by MA-CCP method reached a submicrometer.     

Preparation and luminescent properties of CaAl_2O_4:Eu~(3+),R~+(R=Li,Na,K) phosphors

CaAl2O4:Eu3+,R+(R=Li+,Na+,K+) red phosphors were synthesized by solid state reaction method.X-ray diffraction(XRD) and photoluminescence(PL) were employed to characterize their structural and luminescent properties.It was found that the optimal sintering temperature and sintering time were 1200 °C and 4 h,respectively.The optimal concentration of doped Eu3+ was 3 mol.%.Furthermore,under ultraviolet excitation with a wavelength of 254 nm,these samples showed red luminescence which were probably attributed to the transitions from 5D0 excited state to 7FJ(J=0-4) ground states of Eu3+ ions.The feature and the high intensity of hypersensitive transition from 5D0→7F2 indicated that Eu3+ preferred to occupy a low symmetry site.The incorporation of alkali metal ions greatly enhanced the luminescence intensity probably due to the influence of charge compensation of alkali metal ions.     

Experimental charge density distribution and its correlation to structural and optical properties of Sm~(3+) doped Nd_2O_3 nanophosphors

Pure and Sm~(3+) doped Nd_2 O_3 nanophosphors were synthesized using modified Pechini method. The phase formation with symmetry of the sample is confirmed by the Rietveld refinement of the powder Xray diffraction(PXRD) data. The surface morphology and the crystallite size were examined using scanning electron microscopy(SEM) and transmission electron microscopy(TEM) and the results confirmed that the synthesized particles are in nanosize. The energy-dispersive X-ray(EDX) analysis was done to confirm the purity of the sample. The optical properties of the sample were studied using ultraviolet-visible range(UV-Vis) spectroscopic analysis and photoluminescence studies. The calculated band gap of the synthesized Nd_2 O_3 was found to be higher than that of bulk Nd_2 O_3. The photoluminescence(PL) of the prepared samples reveals that doping with Sm3+ ion has influenced the optical properties. Quantitative investigation on charge density distribution was done by analysing the 3-dimensional and 2-dimensional charge density maps drawn along the bonding directions. The maximum entropy method(MEM)/Rietveld analysis was used for the first time to analyse the charge density in the chosen system. Charge density arrangement in the unit cell is correlated to the analysed photoluminescent(PL) properties. The spectral behaviour of the samples has been explained through charge ordering which are verified using experimental data obtained. The studies on these materials have shown that these nanophosphors will provide promising application for near-ultraviolet lightemitting diodes(n-UV-LEDs).     

NMR Study on Structural Characteristics of Rare Earth Doped Boro-Alumino- Silicate Glasses

The structural characteristics of Re2O3 doped B2O3-Al2O3-SiO2 glasses and factors such as the component and heat-treating conditions affecting the glass structure were investigated by magic angle spin nuclear magnetic resonance （MAS NMR） spectroscopy and differential thermal analysis （DTA）. It is found that, in B2O3-Al2O3-SiO2 glass, the boron （4）, and Al（5）, Al（6） changes to Al（4）. On the other hand, compared with Ba^2＋ , RE^3＋ can accumulate the boron network because of its higher field strength, which results in a large network structure. With the increase of samarium oxide, the silicate coordination Qa（3T） will have predominance gradually. Heat-treatment has little effect on the boron and aluminum coordination sites in the glass structure.     

Influence of Y~(3+),Yb~(3+),Gd~(3+) cations on structural and electromagnetic properties of CuFe_2O_4 nanoferrites prepared via one step sol-gel method

Rare earths(REs) play a key role in distorting spinel structure by creating some defects at the lattice sites and make them suitable for magnetodielectric applications.In the present study,the nanoferrites of CuRE_(0.02)Fe_(1.98)O_4,where REs=Y~(3+),Yb~(3+),Gd~(3+),were prepared using one step sol-gel method.The prepared samples are copper ferrite(CFO),yttrium doped copper ferrite(Y-CFO),ytterbium doped copper ferrite(Yb-CFO) and gadolinium doped copper ferrite(Gd-CFO),respectively.The single-phase structure of all the REs doped nanoferrites was determined by X-ray diffraction(XRD) analysis.The porosity,agglomerations and grain size of the REs doped copper ferrite were examined using field emission scanning electron microscopy(FESEM) analysis.Fourier transform infrared spectroscopy(FTIR)elaborates the phase formation and environmental effects on the REs doped nanoparticles(NPs).The recorded room temperature M-H loops from a vibrating sample magnetometer(VSM) elucidate the magnetic properties of the REs doped spinel nanoferrites.The magnetic saturation(M_s) was calculated in the range of 23.08 to 51.78 emu/g.The calculated coercivity values(272.6 to 705.60 Oe) confirm the soft magnetic behavior of REs doped copper ferrites.Furthermore,the electromagnetic and dielectric properties were assessed using a Vector network analyzer(VNA) from 1 to 6 GHz.The permeability,permittivity,dielectric tangent loss and electric modulus of the REs doped spinel ferrites illustrate that the prepared NPs may be suitable for microwave and high frequency applications.     

Reduction of Tb~(4+) ions in luminescent Y_2O_3:Tb nanorods prepared by microwave hydrothermal method

Terbium doped yttrium oxide was prepared with the microwave hydrothermal method. The Y_2O_3:Tb nanomaterial crystallized as needle-like grains. Bright luminescence in the green region was observed. Significant luminescence intensity increase was obtained after thermal treatment. Reduction of terbium ions was observed after heating in the air atmosphere. Tb~(4+) ions were found to be stabilized by crystal impurities. Hydroxyl species were found to have impact on vacancies elimination. The terbium ions were used as optical and magnetic indicator of the material properties.     

Color vision and color preference in Japanese quail (Coturnix coturnix japonica) with colorless oil droplets.

Studied the significance of the coloration of retinal oil droplets in the color vision of 90 young quail. Colorless oil droplets were produced in Ss by dietary exclusion of carotenoids in their mothers. Carotenoid-free chicks were able to distinguish red, yellow, green, and blue of constant intensity from white light of different intensities. This indicates that the colored oil droplets are not essential in the color vision of quail. Testing color preferences by offering the 4 primary colors in 6 paired combinations indicated that normal Ss as well as Ss with colorless oil droplets preferred green the most and red the least. However, carotenoid-free Ss were different from controls in preferring blue over yellow. (38 ref) (PsycINFO Database Record (c) 2010 APA, all rights reserved)     

CsBaB_3O_6:Eu~(3+) red-emitting phosphors for white LED and FED:Crystal structure,electronic structure and luminescent properties

Recently,borate compounds have received much attention in the field of rare earth doped phosphors due to their excellent luminescent performance.In this work,to explore the potential in LED and FED applications,the CsBaB_3 O_6:Eu~(3+) phosphor was investigated in detail by using Rietveld refinement,DFT calculations,photoluminescent and cathodoluminescent spectra.As a result,CsBaB_3 O_6 has a planar stacked three-dimensional layered structure.Under the excitation of 395 nm n-UV light and electron beam,CsBaB_3 O_6:Eu~(3+) phosphor exhibits a typical red emission of Eu~(3+).A good thermal stability and good resistance to saturation and degradation were observed in the CsBaB_3 O_6:Eu~(3+) phosphor.The related photoluminescent and cathodoluminescent mechanisms were studied.The results indicate that CsBaB_3 O_6:Eu~(3+) phosphor has potential in multifunctional applications.     

Optical performance study of Sr_2ZnSi_2O_7:Eu~(2+),Dy~(3+), SrAl_2O_4:Eu~(2+),Dy~(3+) and Y_2O_2S:Eu~(3+),Mg~(2+),Ti~(4+) ternary luminous fiber

In this study, down-conversion fluorescent powder of Sr_2ZnSi_2O_7:Eu~(2+),Dy~(3+), SrAl_2O_4:Eu~(2+),Dy~(3+) and Y_2O_2S:Eu~(3+),Mg~(2+),Ti~(4+), which were the common three primary colors materials with long afterglow, were synthesized by high temperature solid state method. The blends of rare earth(RE) luminescent materials have been of interest to reinvest the luminescent characteristics of polyethylene terephtahalate(PET) luminous fiber. The scanning electron microscopy(SEM) and an inversion fluorescence microscope were used to characterize the surface morphology and the dispersion of inclusion. Through analysis of microcosmic morphology, three typical dispersions of luminescent particles were summarized. The X-ray diffraction indicated that the phase structure of fiber samples and crystal structure of luminescence materials kept complete after prilling and spinning. From the fluorescence spectra and CIE 1931 coordinates, it could be found that different combinations of luminous fibers were desired to obtain divers colors emission luminous fiber. And the fiber samples were a light sensation which could induct different excitation wavelengths and convert it down to different colors. The afterglow decay curve and its differential curve were summarized indicating the three decay stages. The decay curve and decay rate curve showed that the contents of Sr_2ZnSi_2O_7:Eu~(2+),Dy~(3+), SrAl_2O_4:Eu~(2+),Dy~(3+) and Y_2O_2S:Eu~(3+),Mg~(2+),Ti~(4+) had obvious influence on the afterglow of fiber samples.     

Broadband near-infrared luminescence and energy transfer of Cr~(3+),Ce~(3+) co-doped Ca_2LuHf_2Al_3O_(12) phosphors

Broadband near-infrared phosphors are highly desirable for food testing.Targeted Ca₂LuHf₂Al₃O₁₂:Cr³⁺(CLHA:Cr³⁺) and Ca₂LuHf₂Al₃O₁₂:Ce³⁺,Cr³⁺(CLHA:Ce³⁺,Cr^(³⁺)) phosphors were synthesized by the conventional high-temperature solid state reaction.The CLHA:Cr³⁺phosphor,with a good thermal stability,shows a red shift owing to radiation reabsorption and non-radiative transition with increasing Cr³⁺content.For co-doped sample,the emission intensity of Cr³⁺can be enhanced by three times due to the energy transfer from Ce³⁺to Cr³⁺,which can be evidenced by a significant overlap between the PLE of Cr³⁺single-doped phosphor and the PL of Ce³⁺single-doped phosphor.In addition,the mechanism of energy transfer is identified as a quadrupole-quadrupole interaction according to decay Lifetime and Dexter’s energy transfer formula.The broadband NIR emission peaked at 775 nm of CLHA:Cr³⁺,Ce³⁺phosphor shows a bright prospect in nondestructive quality-control analysis systems for food.     

Photoluminescence properties of Ca-doped BaMg Al10O17）：Eu2＋,Mn2＋ blue phosphor using BaF2 and CaF2 as co-flux

Ca-doped Ba Mg Al10O17：Eu2＋,Mn2＋（BAM） blue phosphors were synthesized by flux assisted solid-state reaction method using Ca F2 and Ba F2 as co-flux.Good dispersity and particle size homogenization of hexagonal pure phase BAM were obtained by sintering at 1400 ℃.The effects of the Ca2＋ ions content on the structure, morphology and photoluminescence properties of the phosphors were studied.The results indicated that the incorporation of Ca could decrease the lattice constant, improve the homogeneity and dispersity and enhance the photoluminescence（PL） intensity of the phosphor effectively.The optimum Ba0.86Ca0.04Mg0.97Al10O17：0.1Eu2＋,0.03Mn2＋ PL intensity was enhanced for about 30% and relative brightness was improved about 4%.Furthermore, the synthesized BAM and commercial BAM phosphors were annealed for 30 min at 600 oC in air.The Ca-doped phosphors had stronger emission intensity, higher brightness and better chromaticity stability than that of the commercial phosphor.These results indicated that Ca-doped blue phosphors had good potential applications in the commercial tricolor fluorescent lamps as well as in other display and lamps.     

A terbium activated multicolour photoluminescent phosphor for luminescent anticounterfeiting

The multicolor photoluminescence(PL) of a Tb~(3+)singly activated NaYGeO_4 phosphor is prepared by solid state method.For the first time,it is reported that the PL color of Tb~(3+)in NaYGeO_4 phosphor can be tuned from green to blue and,finally,to red by controlling the Tb~(3+)content.The optimal tricolor phosphors are NaYGeO_4:0.01 mol% Tb~(3+)(red),NaYGeO_4:0.5 mol% Tb~(3+)(blue) and NaYGeO4:5 mol% Tb~(3+)(green),respectively.The PL properties of the NaYGeO_4:Tb~(3+) phosphor were studied in details.The results reveal that the PL color modulations of the NaYGeO_4:Tb~(3+)phosphor are essentially due to the cross-relaxation effect of Tb~(3+),and a possible mechanism on the cross-relaxation is proposed.According to these unique features,a multicolor PL image was fabricated based on the NaYGeO_4:Tb~(3+) phosphor for potential applications in luminescent anticounterfeiting.