scholarly journals Luminescence Properties of Eu- and Mg-Codoped Sol-Gel SiO2 Glasses

2012 ◽  
Vol 2012 ◽  
pp. 1-5 ◽  
Author(s):  
Martin O. Onani ◽  
Paul Mushonga ◽  
Lehlohonolo F. Koao ◽  
Francis B. Dejene

A series of SiO2 nanostructures codoped with Eu3+; Mg2+ ions were obtained by a sol-gel method. The gels synthesized by the hydrolysis of Si(OC2H5)4, Eu(NO3)3·6H2O, and Mg(NO3)2 were heated in air at 600°C for 2 hours. Firstly, the total amount of Eu3+ ions was varied from 0 to 2.0 mol% to investigate the effect of self-damping, while in the second case, the Eu3+ ions were kept constant in the experiment at 0.5 mol% total doping and Mg2+ ions varied. The samples were characterized by X-ray diffraction, TEM, EDS, and UV lamp-excited luminescence spectroscopy. The Eu3+ ions were homogeneously dispersed in the silica and interacting with the small (1–5 nm) amorphous silica matrix. Strong red emissions located at 614 nm and 590 nm for doped and codoped SiO2 were observed from the UV light excitation at room temperature. The composition of around 1.25 mol% Eu3+ gave highest emission intensity. SiO2; Mg2+ ions portray strongly enhanced emissions due to energy transfer from Mg2+ to Eu3+, which is due to radiative recombination. An increase in luminescence intensity was observed as the Mg2+-to-Eu3+ ratio increased for the range investigated. The results show Eu3+ ion is located inside or at the surface of disordered SiO2 nanoparticles.


2001 ◽  
Vol 676 ◽  
Author(s):  
Carla Cannas ◽  
Mariano Casu ◽  
Roberta Licheri ◽  
Anna Musinu ◽  
Giorgio Piccaluga ◽  
...  

ABSTRACTA Y2O3-SiO2 nanocomposite doped with Eu3+ was obtained by a sol-gel method and characterized by X-ray diffraction, IR, 29Si NMR and laser-excited luminescence spectroscopy. It was found that small (2-3 nm) yttria nanoparticles are homogeneously dispersed in, and interacting with, the amorphous silica matrix. Luminescence spectroscopy indicates that the Eu3+ ion is preferentially located inside or at the surface of highly disordered Y2O3 nanoparticles. These luminescent nanocomposites form a class of materials which could find applications in the field of phosphors.



2002 ◽  
Vol 16 (06n07) ◽  
pp. 1047-1051
Author(s):  
JIANPING MA ◽  
ZHIMING CHEN ◽  
GANG LU ◽  
MINGBIN YU ◽  
LIANMAO HANG ◽  
...  

Intense photoluminescence (PL) has been observed at room temperature from the polycrystalline SiC samples prepared from carbon-saturated Si melt at a temperature ranging from 1500 to 1650°C. Composition and structure of the samples have been confirmed by means of X-ray photoelectron spectroscopy, X-ray diffraction and scanning electron microscopy. PL measurements with 325 nm UV light excitation revealed that the room temperature PL spectrum of the samples consists of 3 luminescent bands, the peak energies of which are 2.38 eV, 2.77 eV and 3.06 eV, respectively. The 2.38 eV band is much stronger than the others. It is suggested that some extrinsic PL mechanisms associated with defect or interface states would be responsible to the intensive PL observed at room temperature.



2018 ◽  
Vol 233 (2) ◽  
pp. 73-79 ◽  
Author(s):  
Dan Zhao ◽  
Fa-Xue Ma ◽  
Bao-Zhong Liu ◽  
Yun-Chang Fan ◽  
Xue-Feng Han ◽  
...  

AbstractSingle crystals of two cesium rare-earth molybdates CsLn(MoO4)2(Ln=Eu, Tb) have been prepared using the high temperature molten salt (flux) method. Single-crystal X-ray diffraction analyses reveal that they crystallize in the orthorhombic space groupPccm(No. 49) and features a 2D layer structure that is composed of [Ln(MoO4)2]∞and [Cs]∞layers. Under near-UV light excitation, emission spectrum of CsEu(MoO4)2consists of several sharp lines due to the characteristic electronic transitions of Eu3+ions, whereas CsTb(MoO4)2exhibits characteristic green emission of Tb3+ions.



2016 ◽  
Vol 2016 ◽  
pp. 1-8 ◽  
Author(s):  
C. R. García ◽  
L. A. Diaz-Torres ◽  
J. Oliva ◽  
M. T. Romero ◽  
P. Salas

Blue phosphorescent strontium aluminosilicate powders were prepared by combustion synthesis route and a postannealing treatments at different temperatures. X-ray diffraction analysis showed that phosphors are composed of two main hexagonal phases: SrAl2O4and Sr3Al32O51. The morphology of the phosphors changed from micrograins (1000°C) to a mixture of bars and hexagons (1200°C) and finally to only hexagons (1300°C) as the annealing temperature is increased. Photoluminescence spectra showed a strong blue-green phosphorescent emission centered atλem=455 nm, which is associated with4f65d1→4f6  (8S7/2)transition of the Eu2+. The sample annealed at 1200°C presents the highest luminance value (40 Cd/m2) with CIE coordinates (0.1589, 0.1972). Also, the photocatalytic degradation of methylene blue (MB) under UV light (at 365 nm) was monitored. Samples annealed at 1000°C and 1300°C presented the highest percentage of degradation (32% and 38.5%, resp.) after 360 min. In the case of photocatalytic activity under solar irradiation, the samples annealed at 1000°C, 1150°C, and 1200°C produced total degradation of MB after only 300 min. Hence, the results obtained with solar photocatalysis suggest that our powders could be useful for water cleaning in water treatment plants.



2018 ◽  
Vol 762 ◽  
pp. 408-412
Author(s):  
Raivis Eglītis ◽  
Gundars Mežinskis

In this work two different hydrosols were used to impregnate a commercially available cotton fabric with anatase nanoparticles to give it photocatalytic activity. To increase the activity, different pre-treatment methods were applied. The nanoparticle size was determined using dynamic light scattering and x-ray diffraction and the fabrics were examined using scanning electron microscopy. Photocatalytic activity was measured using the degradation of methyl-orange while irradiating the samples with UV light. The synthesis method allowed to produce anatase with an average particle size of 32 to 37 nm depending on the synthesis method used.



1995 ◽  
Vol 398 ◽  
Author(s):  
C. Barrera-Solano ◽  
M. PiÑero ◽  
C. Jiménez-Solís ◽  
L. Gago-Duport

ABSTRACTYSZ samples containing 5 and 10 mol% of Y203 were prepared by controlled hydrolysis of metal alkoxides. The dried powders were calcined at 800°C and then they were uniaxially pressed and sintered at different temperatures and next heated at 1400°C (∼ 5 MPa) or annealed at 1600°C for 24 h. The quantitative analysis of the experimental X-ray diffraction (XRD) spectra was performed by Whole Pattern Fitting (WPF). A Pseudo-Voigt (Thompson-Cox-Hastings) was used as shape profile function. The respective phase fractions (wt %) were fitted for both solid state solutions using the scale factor. The heat treatment induced changes are discussed.



2019 ◽  
Vol 75 (7) ◽  
pp. 883-890 ◽  
Author(s):  
Ya-Li Xue ◽  
Ai-Yun Zhang ◽  
Xiao-Yang Han ◽  
Xiao-Qi Cui ◽  
Ling Deng ◽  
...  

An anhydrous orthophosphate, K3Eu5(PO4)6 (tripotassium pentaeuropium hexaphosphate), has been prepared by a high-temperature solid-state reaction combined with hydrothermal synthesis, and its crystal structure was determined by single-crystal X-ray diffraction analysis (SC-XRD). The results show that the compound crystallizes in the monoclinic space group C2/c and the structure features a three-dimensional framework of [Eu5(PO4)6]∞, with the tunnel filled by K+ ions. The IR spectrum, UV–Vis spectrum and luminescence properties of polycrystalline samples of K3Eu5(PO4)6, annealed at temperatures of 650, 700, 750, 800 and 850 °C, were investigated. Although with a full Eu3+ concentration (9.96 × 1021 ions cm−3), the self-activated phosphor K3Eu5(PO4)6 shows s strong luminescence emission intensity with a quantum yield of 37%. Under near-UV light excitation (393 nm), the series of samples shows the characteristic emissions of Eu3+ ions in the visible region from 575 to 715 nm. The sample sintered at 800 °C gives the strongest emission and its lifetime sintered at 800 °C (1.88 ms) is also the longest of all.



2002 ◽  
Vol 17 (3) ◽  
pp. 590-596 ◽  
Author(s):  
G. Ennas ◽  
M. F. Casula ◽  
G. Piccaluga ◽  
S. Solinas ◽  
M. P. Morales ◽  
...  

γ–Fe2O3/SiO2 and Fe/SiO2 nanocomposites, with a Fe/Si molar ratio of 0.25, were prepared by the sol-gel method starting from ethanolic solutions of tetraethoxysilane and iron (III) nitrate. After gelation the xerogels were oxidated or reduced. Samples were investigated by transmission electron microscopy, x-ray diffraction, differential scanning calorimetry, and thermogravimetry. Magnetic properties of the samples were investigated at room temperature (RT) and at 77 K. Nanometric particles supported in the silica matrix were obtained in all cases. Bigger particles (10 nm) were obtained in the case of Fe/SiO2 nanocomposites with respect to the γ–Fe2O3/SiO2 samples (5–8 nm). A slight effect of sol dilution on particle size was observed only in the case of γ–Fe2O3/SiO2 nanocomposites. A superparamagnetic behavior was shown at RT only by γ–Fe2O3/SiO2 nanocomposites. Iron-based composites exhibited coercivity values higher than 700 Oe at RT.



2013 ◽  
Vol 401-403 ◽  
pp. 796-799 ◽  
Author(s):  
Jia Yue Sun ◽  
Dian Peng Cui ◽  
Bing Xue ◽  
Guang Chao Sun

Single-phase Ba5(PO4)3Cl:Ce3+,Tb3+ (BPCl:Ce3+,Tb3+) samples have been synthesized via solid-state reaction method. The phase structure and luminescence properties are characterized using powder X-ray diffraction (XRD), photoluminescence excitation and emission spectra. Effective energy transfer occurs from Ce3+ to Tb3+ due to the observed spectral overlap between the emission band of Ce3+ and the excitation band of Tb3+. Ce3+/Tb3+-codoped Ba5(PO4)3Cl shows more intense yellowish-green light compared to that of Tb3+-doped sample under UV light excitation.



2011 ◽  
Vol 393-395 ◽  
pp. 1287-1290
Author(s):  
Min Wang ◽  
Qiong Liu ◽  
Qi Xing

The N-doped Cu11O2 (VO4)6 photocatalyst was prepared using the sol-gel method. Techniques of X-ray diffraction (XRD), scanning electron microscope (SEM) have been employed to characterize the as-synthesized materials. During liquid phase photocatalytic degradation of Methy lorange(MO) under the UV-light, the as-prepared N-doped Cu11O2 (VO4)6 exhibits higher activity than the pure Cu11O2 (VO4)6 without doped N. It found that the N-doped Cu11O2 (VO4)6 prepared with the molar ratio of citric acid to metal inons be 2:1, N/Cu molar ratio of 12%, pH=7 and calcinated under 500°C for 4 hours was pure triclinic phase. In this conditions, the sample had highest photocatalytic activity with the photodegradation rate was about 94.42% or so in 60min under 20W ultraviolet lamp.



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