Upconversion luminescence of Y_2O_3:Er^(3+), Yb^(3+) nanoparticles prepared by a homogeneous precipitation method

Y2O3： Er^3＋, Yb^3＋ nanoparticles were synthesized by a homogeneous precipitation method without and with different concentrations of EDTA 2Na. Upconversion luminescence spectra of the samples were studied under 980 nm laser excitation. The results of XRD showed that the obtained Y2O3：Er^3＋,Yb^3＋ nanoparticles were of a cubic structure. The average crystallite sizes calculated were in the range of 28-40 nm. Green and red upconversion emission were observed, and attributed to ^2H11/2,^4S3/2→^4I15/2 and ^4F9/2→^4I15/2 transitions of the ion, respectively. The ratio of the intensity of green emission to that of red emission drastically changed with a change in the EDTA 2Na concentration. In the sample synthesized without EDTA, the relative intensity of the green emission was weaker than that of the red emission. The relative intensities of green emission increased with the increased amount of EDTA 2Na used. The possible upconversion luminescence mechanisms were discussed.

Synthesis and luminescence properties of nanocrystalline Gd_3Ga_5O_(12):Eu^(3+) by a homogeneous precipitation method

Nanocrystalline Gd3Ga5O12:Eu3+ with cubic phase was prepared by a urea homogeneous precipitation method. X-ray diffraction (XRD), field emission scanning electron microscopy (SEM), Fourier transform infrared spectroscopy (FT-IR), thermo-gravimetric and differential thermal analysis (TG-DTA) and photoluminescence spectra were used to characterize the samples. The effects of the initial solution pH value and urea content on the structure of the sample were studied. The XRD results show that pure phase Gd3Ga5O12 can be obtained at pH =6 and pH =8 of the initial solution. The average crystallite size can be calculated as in the range of 24~33 nm. The average crystallite size decreases with increasing molar ratio of urea to metal ion. The results of excitation spectra and emission spectra show that the emission peaks are ascribed to 5D0→7FJ transitions of Eu3+, and the magnetic dipole transition originated from 5D0 →7F1 of Eu3+ is the strongest; the broad excitation bands belong to change transfer band of Eu?O and the host absorption of Gd3Ga5O12. An efficient energy transfer occurs from Gd3+ to Eu3+.

Preparation and Characteristics of Hydroxyapatite Whiskers by Homogeneous Precipitation Method

Hydroxyapatite whilkers were prepared by the homogeneousprecipitation method. Soluble calci- um ion and phosphate ion wereused as initial materials, they were refluxed respectively at 85 deg.C, 90 deg. C and 95 deg. C for various lengths of time. A properprecipitation agent was selected to control the releasing speed ofions in the system; it induced the hydroxyapatite crystal to grow indesired way. The pH each solutions were mea- sured continuouslyduring the reaction.

Effect of Yb^(3+) concentration on the structures and upconversion luminescence properties of Y_2O_3:Er^(3+) ultrafine phosphors

Y2O3：Er^3＋ ultrafine phosphors with a varying Yb^3＋ ion concentration were prepared by a urea homogeneous precipitation method. The results of XRD show that all the samples are of a pure cubic structure and the average crystallite sizes can be calculated as 45, 34, and 28 nm for Y2O3：Er^3＋ ultrafine phosphors with Yb^3＋ ion concentrations of 0, 10%, and 20%, respectively. The lattice constant and cell volume of the ultrafine phosphors decrease with enhancing Yb^3＋ ion concentration. The upconversion luminescence spectra of all the samples were studied under 980 nm laser excitation. The strong green and red upconversion emission were observed, and attributed to the ^2H11/2→^4I15/2, ^4S3/2 → ^4I15/2 and ^4F9/2 →^4I15/2 transitions of Er^3＋, respectively. The intensity of red emission increases with increasing Yb^3＋ ion concentration. The effect of Yb^3＋ ion concentration on the structures and upconversion luminescence mechanism were discussed.

Influential Factors on Morphology of Hydroxyapatite Crystals

Needle like hydroxyapatite crystals were synthesized by homogeneous precipitation method with water soluble calcium salts and phosphates.The work focuses on the analysis of influencing factors on length and lengh/diameter ratio of hydroxyapatite crystals,which are main characteristics of reinforcement materials.The effects caused by system temperature,concentration of nutrient,and additives are discussed,and the optimum reacting condition is given.

Promoting effect of tantalum and antimony additives on deNOx performance of Ce3Ta3SbOx for NH3-SCR reaction and DRIFT studies

A superior Ce-Ta-Sb composite oxide catalyst prepared using homogeneous precipitation method exhibited excellent deNOx efficiency and nearly 100% Nselectivity with broad operation temperature window and better resistance to higher space velocity, meanwhile strong resistance to HO and SO. This catalyst was systematically characterized using XRD, Nadsorption, SEM, TEM, XPS, ESR, Raman, H-TPR,NH3-TPD and in situ DRIFTS. There exists a synergistic effect between Ce, Ta and Sb species. It is further indicated that the prominent deNOx performance of the Ce3 Ta3 SbOx catalyst is attributed to the elevated Ce3+ concentrations, abundant active surface oxygen species, as well as surface acidity and reducibility,which is closely linked with the synergistic effect between Ce, Sb and Ta species. Results from DRIFTS reveal that the reaction mechanism of surface-adsorbed NH3 and NOspecies is linked to temperature,the L-H mechanism mainly occurs at low temperature(<300 ℃),while the E-R mechanism occurs at high temperature(>300 ℃). Overall,these findings indicate that Ce3 Ta3 SbOx is promising for NOpractical abatement.

Effect of Ce doping of TiO_2 support on NH_3-SCR activity over V_2O_5–WO_3/CeO_2–TiO_2 catalyst

CeO2–TiO2composite supports with different Ce/Ti molar ratios were prepared by a homogeneous precipitation method, and V2O5–WO3/CeO2–TiO2catalysts for the selective catalytic reduction（SCR） of NOx with NH3 were prepared by an incipient-wetness impregnation method. These catalysts were characterized by means of BET, XRD, UV–Vis,Raman and XPS techniques. The results showed that the catalytic activity of V2O5–WO3/TiO2 was greatly enhanced by Ce doping（molar ratio of Ce/Ti = 1/10） in the TiO2 support.The catalysts that were predominantly anatase TiO2 showed better catalytic performance than the catalysts that were predominantly fluorite CeO2. The Ce additive could enhance the surface adsorbed oxygen and accelerate the SCR reaction. The effects of O2 concentration, ratio of NH3/NO, space velocity and SO2 on the catalytic activity were also investigated. The presence of oxygen played an important role in NO reduction. The optimal ratio of NH3/NO was 1/1 and the catalyst had good resistance to SO2 poisoning.