Pb2+ and Ce3+ Doped SrZnO2: New Blue Luminescent Phosphors

2006 ◽  
Vol 916 ◽  
Author(s):  
Alp Manavbasi ◽  
Jeffrey C LaCombe

AbstractTwo new blue emitting phosphors, SrZnO2:Pb2+ and Ce3+ were synthesized by adipic acid and sucrose templated sol-gel routes, respectively. The resulting phosphor particles were fine, nanocrystalline and pure. The optimum activator concentrations were found to be 1 mol% Pb2+ and 12 mol% Ce3+. Two excitation bands centered at 283 and 317 nm, plus a weak shoulder at 275 nm were observed for Pb2+ doped samples, however only one broad excitation band with a maximum at 294 nm was observed for Ce3+ doped samples fired at 1000 °C for 2h. The emission spectra of SrZnO2:Pb2+ showed a very broad band extending from 374 to 615 nm with a maximum at ~455 nm which was ascribed to the 3P1 ¡æ 1S0 transition on the Pb2+ ions allowed by the strong spin-orbit (SO) coupling. Similarly, SrZnO2:Ce3+ showed a broad emission band extending from 374 to 609 nm and centered at 467 nm. This broad emission was attributed to the 5d1 ¡æ 4f1 transition of Ce3+ ions. The lower level 2F5/2 of the 4f1 is populated but the level 2F7/2 is almost empty at room temperature where all measurements were taken. The luminescence properties of Ce3+, K+ co-doped SrZnO2 revealed that the characteristic band locations remained the same and the ratio of emission to excitation intensities were constant. X-ray diffraction patterns showed that the SrZnO2 phase started to form at 900 °C (after 2 hrs), and the single-phase SrZnO2 obtained at 1000 °C. SEM micrographs of both phosphors have a rounded and filled morphology for individual particles with an approximate diameter of 50-250 nm. Dynamic light scattering studies revealed that average particle size is around 1 ¥ìm for both phosphors.

2021 ◽  
Author(s):  
Mahesh Gaidhane ◽  
Deepak Taikar ◽  
Pravin Gaidhane ◽  
Kalpana Nagde

Abstract Nanocrystalline α-Fe2O3 is synthesized by sol-gel technique. The prepared nanomaterial was characterized by X-ray diffraction (XRD), SEM, TEM, Fourier Transform Infrared (FTIR) spectroscopy, Vibrating Sample Magnetometry (VSM) and photoluminescence (PL) techniques. X-ray powder diffraction analysis confirmed the formation of α-Fe2O3. Electron microscopy showed spherical morphologies with an average particle size of 30-40 nm. The magnetic property of the prepared material was studied by VSM at room temperature. VSM study shows superparamagnetic nature of the synthesized nanoparticles. Photoluminescence (PL) emission spectra show intense broad emission band centered at 570 nm with 393 nm excitation indicating its usefulness for w-LED application. The CIE-chromaticity color coordinates of prepared material were calculated. The photocatalytic activity of the α-Fe2O3 nanoparticles was analyzed and the nanopowder exhibited good photocatalytic activity for the removal AO7 from its aqueous solution.


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.


2011 ◽  
Vol 412 ◽  
pp. 271-274
Author(s):  
Ying Li ◽  
Qiang Xu ◽  
Ling Dai

In order to prepare ultrafine La3NbO7 powder, a potential material for thermal barrier coatings, the calcination process of La3NbO7 was studied in this paper.The precursor of La3NbO7 was synthesized by using a citric acid complex method. A calcination process had been systematically investigated. The reaction temperature was determined by differential scanning calorimetry (DSC). The phase composition of powders was characterized by X-ray diffraction (XRD), and the morphology was obtained by scanning electron microscope (SEM). The results revealed that the single-phase La3NbO7 powder could be successfully prepared while the calcination temperature exceeded 800°C and a better morphology could be maintained at 800°C for 4 hours. Considering all above, an optimum calcination scheme was adopted at 800°C for 4 hours. The as-prepared La3NbO7 powders had a grain size of about 50nm and an average particle size of about 300nm.


2011 ◽  
Vol 04 (01) ◽  
pp. 101-105 ◽  
Author(s):  
S. SELMANI ◽  
H. ABDULLAH ◽  
S. SHAARI ◽  
R. ABD-SHUKOR

Nanoparticles of Zn (1-x) Fe x S with x = 0.0, 0.05, 0.1, 0.15, 0.2 and 0.3 were synthesized using the chemical bath deposition method, using tri-sodium citrate as a complexion agent. These nanoparticles were characterized using XRD, SEM, optical absorbance and photoluminescence. SEM micrographs of the films revealed the combination of Zn (1-x) Fe x S nanoparticles with an average particle size D ~ 60.3 to 19.3 nm ± 0.01 nm for x = 0.0 to 0.3. X-ray diffraction patterns confirmed the nanocrystalline cubic ZnS phase formation. UV-visible spectrometer measurement showed high absorbance for Fe concentration x ≥ 0.15 in the wavelength range 325–800 nm. However, for x ≤ 0.1, the absorbance of the films decreased with further increase of Fe concentration. From the absorbance data, the direct bandgap values have been calculated to be in the range Eg = 3.5 to 2.23 eV for x = 0.0 to 0.3. The bandgap decreased with the increase of Fe concentration in the films. The photoluminescence spectra of the films showed two emission peaks, the first in the low wavelengths due to band-to-band transition, and the second in the high wavelengths due to the transitions probabilities and to the concentration of Fe ions. Due to the quenching effect, the intensity of PL spectra decreased on further increase of Fe doping.


2006 ◽  
Vol 45 ◽  
pp. 1803-1808 ◽  
Author(s):  
I.C. Cosentino ◽  
E.N.S. Muccillo ◽  
F.M. Vichi ◽  
R. Muccillo

Ceramic ZrTiO4 powders were prepared by a sol-gel method using zirconium oxychloride and titanium tetraisopropoxide. In situ high temperature X-ray diffraction results show that crystallization of the amorphous gel starts at 400°C. Single-phase ZrTiO4 nanoparticles of 46 nm average particle size, determined by nitrogen adsorption analysis, were obtained after heat treatment at 450°C for 1 h. After pressing these sinteractive powders, pellets with controlled pore size distribution were obtained by sintering at temperatures as low as 400°C. The analysis of pores by mercury porosimetry gives an average porosity of 45%. The electrical resistivity, determined by impedance spectroscopy measurements at 24°C under different humidity environments, shows the ability of these pellets to adsorb water vapor in the porous surfaces.


2014 ◽  
Vol 2014 ◽  
pp. 1-10 ◽  
Author(s):  
Fernanda Malaquias Barboza ◽  
Willian Moreira Machado ◽  
Luiz Renato Olchanheski Junior ◽  
Josiane Padilha de Paula ◽  
Sônia Faria Zawadzki ◽  
...  

Microparticles of poly(ε-caprolactone) (PCL) and poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBV) containing manidipine dihydrochloride (MAN) were successfully prepared by the simple emulsion/solvent evaporation method. All formulations showed loading efficiency rates greater than 80% and average particle size less than 8 μm. Formulations had spherical shape with smooth and porous surface for PCL and PHBV, respectively. According to Fourier-transform infrared spectroscopy, initial components were not chemically modified during microencapsulation. X-ray diffraction patterns and differential scanning calorimetry demonstrated that this process led to drug amorphization.In vitrodissolution studies showed that all microparticles prolonged MAN release, mainly which one obtained using PCL that contained 5% of drug loaded (PCL-M5). Animal studies demonstrated that formulationPCL-M5was able to keep the variation of mean arterial pressure after phenylephrine administration up to 24 hours. These data confirmed the sustained antihypertensive effect of the investigated microparticles. Results provided an experimental basis for using formulationPCL-M5as a feasible carrier for oral controlled release of MAN intended for treating high blood pressure.


2020 ◽  
Vol 11 (1) ◽  
pp. 747-754
Author(s):  
Saja S. Al-Taweel ◽  
Rana S. Al-Taweel ◽  
Hasan M. Luaibi

In this work, zinc oxide nanoparticles (ZnO - NPs) were prepared using a sol-gel methodology and tested for their antibacterial activity against each of the following pathogenic species: Escherichia coli, Klebsiella pneumonia, and Staphylococcus aureus by well diffusion assay. The sample prepared was characterized by different techniques: Atomic Force Microscope AFM; Fourier Transform Infrared FT-IR; Scanning Electron Microscope SEM and X-Ray Diffraction Spectroscopy XRD. The XRD result showed that ZnO - NPs presence in wurtzite the structure of ZnO. The AFM and SEM of the surface analysis indicate that the most ZnO – NPs appear approximately in a spherical shape with some agglomeration. The average particle size for  ZnO - NPs is nearly 37 nm. Volumes 25µl, 50µl, 75µl, 100µl, 125µl, and 150µl of 10 mg\ ml concentration of  ZnO - NPs were used, the antimicrobial activity results showed that ability for  ZnO - NPs to inhibit the growth of S.aureus increased as the solution volume increased, while the growing of (K. pneumonia) and (E. coli) was inhibited only with the volume 75µl where the inhibition zones diameters were 15mm and 10mm respectively.


2012 ◽  
Vol 15 (2) ◽  
pp. 27-34
Author(s):  
Nguyet Thi Thuy Dao ◽  
Duong Phuc Nguyen ◽  
Hien Duc Than

This paper presents the synthesis and characterization of Y3Fe5O12, Gd3Fe5O12 and Dy3Fe5O12 nanoparticles by sol-gel method using initial salts solution of Y(NO3)3, Gd(NO3)3, Dy(NO3)3, Fe(NO3). The lattice constant, crystallite size and particle morphology of these ferrite garnet nanoparticles were studied by using X-ray diffraction and transmission electron microscopy (TEM). The results showed that the garnet samples prepared by this method were formed at 800oC, which is lower than the sintering temperature for ceramic bulk samples (1400oC). The particle size is in the range 25- 40 nm as observed via TEM image and the average particle size was found to be 37nm using Debye- Scherrer formula.


2021 ◽  
Vol 10 (1) ◽  
pp. 74-78
Author(s):  
Nhan Dang Thi Thanh ◽  
Don Truong Thi ◽  
Thang Le Quoc ◽  
Tien Tran Dong ◽  
Son Le Lam

Presently, biopolymer materials have been given more attention for their outstanding properties, high efficiencies and promising applications in various fields. In this study, Fe2O3/chitosan aerogel-like spheres were successfully prepared from chitosan and FeCl3 by sol–gel process and freeze-drying to provide high-surface area materials. The factors affecting the material synthesis have been studied. The asprepared Fe2O3/chitosan material was characterized by Infrared Spectroscopy (IR), X-ray diffraction (XRD) and Scanning Electron Microscopy (SEM) methods. The results showed that the aerogel spheres have a hollow structure made of chitosan nanofibril networks. Fe2O3 nanoparticles get high crystallinity and have an average particle size of 33 nm.


2018 ◽  
Vol 32 (34n36) ◽  
pp. 1840070 ◽  
Author(s):  
Jinshan Zhang ◽  
Wei Wu ◽  
Fangshi Meng ◽  
Hao Ding ◽  
Jiling Dong

NdFeB nanoparticles were synthesized by a sol–gel method. Firstly, NdFeB gel was prepared by using citric acid and glycol as the gel, and the corresponding salts of Nd, Fe and boric acid. The gel was subsequently annealed under a high temperature condition to obtain NdFeB-oxide phases. Then NdFeB nanoparticles were yielded by reductive annealing of precursors. Microstructure, phase composition and magnetic properties were characterized by X-ray diffraction (XRD), field emission scanning electron microscope (FESEM) and vibrating sample magnetometer (VSM), and also differential scanning calorimetry (DSC) analysis was performed to determine the annealing temperature. At 400[Formula: see text]C, intermediate phases of Fe3BO5 and NdBO3 were formed and stable up to 600[Formula: see text]C; while at 800[Formula: see text]C, they would reacted in presence of oxygen to form NdFeO3 and B2O3. Nd2O3 and Fe2O3 were also formed at this temperature. SEM micrographs of reduced powders after washing process showed an average particle size below 100 nm in all the samples. VSM results showed the oxide powder formed at 800[Formula: see text]C had a coercivity of 1.55 kOe and a saturation magnetization of 1.08 emu/g. The powder synthesized by reduction of oxide powders at 800[Formula: see text]C had a coercivity of 1.02 kOe and a saturation magnetization of 14.17 emu/g.


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