Structural Studies of Pulsed-laser-deposited Ba4Fe4Ti3O16 Oxide Films

2000 ◽  
Vol 15 (6) ◽  
pp. 1389-1396 ◽  
Author(s):  
L. A. Bendersky ◽  
R. Maier ◽  
J. L. Cohn ◽  
J. J. Neumeier

For this paper the pulsed laser deposition on single-crystal MgO substrates of Ba4Fe4Ti3O16 target was studied by transmission electron microscopy and x-ray diffraction. The initial stage of the deposition resulted in the formation of the perovskite Ba(Fe, Ti)O3 phase in an epitaxial, cube-on-cube orientation relationship with a substrate. Further growth of the pseudo-cubic phase was interrupted by the formation of oriented grains with a disordered structure. This disordered structure had a mixture of lamellae of the cubic and hexagonal Ba(Fe, Ti)O3 phases. No formation of the Ba4Fe4Ti3O16 (E) phase was observed. Formation of the disordered phase was explained by the higher stability of hexagonal Ba(Fe, Ti)O3 where accommodation of Fe3+ occurred on a twinning plane. The development of the V-shape morphology and a limited number of orientations of the D structure were explained by the faceting and columnar morphology of the perovskite phase.

2020 ◽  
Vol 2020 ◽  
pp. 1-8
Author(s):  
Edwina Olohirere Uzunuigbe ◽  
Abidemi Paul Kappo ◽  
Sixberth Mlowe ◽  
Neerish Revaprasadu

Synthesizing nanoparticles with the less environmentally malignant approach using plant extract is of great interest; this is because most of the chemical approaches can be very costly, toxic, and time-consuming. Herein, we report the use of Acacia senegal leaf extracts to synthesize silver nanoparticles (AgNPs) using an environmentally greener approach. Silver ions were reduced using the bioactive components of the plant extracts with observable colour change from faint colourless to a brownish solution as indication of AgNP formation. The structural properties of the as-synthesized AgNPs were characterized using powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FTIR), and UV-Vis absorption spectrum. Antimicrobial assessment of the as-synthesized AgNPs was explored on some strains of gram-positive and gram-negative bacteria. The obtained results indicate that the as-synthesized AgNPs are pure crystallite of cubic phase of AgNPs, fairly dispersed with a size range of 10–19 nm. The AgNPs were found to be small in size and exhibit significant antibacterial activities, suggesting that the as-synthesized AgNPs could be used in the pharmaceutical and food industries as bactericidal agents.


1996 ◽  
Vol 427 ◽  
Author(s):  
C. R. Chen ◽  
L. J. Chen

AbstractThermal stability and failure mechanisms of Au/TiW(N)/Si and Au/TiW(N)/SiO2/Si systems have been studied by both conventional and high-resolution transmission electron microscopy, X- ray diffraction and Auger electron spectroscopy. For films deposited in Ar gas containing 20% N2, a single face-centered-cubic phase was the only crystalline phase detected to form. The samples were found to remain stable after annealing at 700 °C for 30 min. The stability temperature for Au/TiW(N)(Ar:N2=80:20)/SiO2/Si samples was found to be higher than those of Au/TiW(N) (Ar:N2=90:10)/SiO2/Si and Au/TiW/SiO2/Si samples.


2017 ◽  
Vol 31 (06) ◽  
pp. 1750037
Author(s):  
M. Ghali ◽  
A. M. Eissa ◽  
M. M. Mosaad

In this paper, we give a microscopic view concerning influence of the growth conditions on the physical properties of nanocrystals (NCs) thin films made of CdS, prepared using chemical bath deposition CBD technique. We show a crystalline phase transformation of CdS NCs from hexagonal wurtzite (W) structure to cubic zincblende (ZB) when the growth conditions change, particularly the solution pH values. This effect was confirmed using X-ray diffraction (XRD), transmission electron microscopy (TEM), optical absorption and photoluminescence (PL) measurements. The optical absorption spectra allow calculation of the bandgap value, [Formula: see text], where significant increase [Formula: see text]200 meV in the CdS bandgap when transforming from Hexagonal to Cubic phase was found.


2019 ◽  
Vol 950 ◽  
pp. 133-137
Author(s):  
Alexander M. Volodin ◽  
Vladimir O. Stoyanovskii ◽  
Vladimir I. Zaykovskii ◽  
Roman M. Kenzhin ◽  
Aleksey A. Vedyagin

Zirconium oxide was obtained via traditional precipitation from a ZrOCl2 solution with ammonia followed by drying at 110 °C. The carbon-coated samples were synthesized by calcination of the pristine zirconia mixed with polyvinylalcohol. The obtained ZrO2@C samples of core-shell structure as well as the reference samples of pristine zirconia were calcined at different temperatures from 500 to 1400 °C. All the materials were examined by a set of physicochemical methods (a low-temperature argon adsorption, transmission electron microscopy, X-ray diffraction analysis, photoluminescence spectroscopy). It was found that the carbon coating prevents the sintering of the oxide nanoparticles, which allows one to maintain the specific surface area, the size of the oxide core and, finally, stabilize its phase composition. Transformation of the cubic phase into monoclinic phase becomes significantly complicated. Thus, 40% of the cubic phase was detected even after calcination of the ZrO2@C sample at 1400 °C. Moreover, the carbon-coated samples treated at elevated temperatures with subsequent removal of the carbon shell were found to possess the highest concentration of the defects related to a presence of the anion vacancies in zirconia.


2014 ◽  
Vol 936 ◽  
pp. 282-286
Author(s):  
Ying Wen Duan

Single-crystalline, epitaxial LaFeO3 films with 5 at. % substitution of Pd on the Fe site are grown on (100) SrTiO3 substrate by pulsed-laser deposition technique. The epitaxial orientation relationships are (110)[001]LFPO||(100)[001]STO. X-ray diffraction and transmission electron microscopy reveal that the LFPO films have high structural quality and an atomically sharp LFPO/STO interface. After reduction treatments of as-grown LFPO films, very little Pd escaped the LFPO lattice onto the film surface, the formed Pd (100) particles are oriented epitaxially, and parallel to the LFPO films surface.


2010 ◽  
Vol 25 (10) ◽  
pp. 2035-2041 ◽  
Author(s):  
Zhiguo Xia ◽  
Peng Du

CaF2:Yb3+,Er3+ upconversion (UC) luminescence nanoparticles have been synthesized using mesoporous silica (SBA-15) as a hard template. The samples were characterized by x-ray diffraction, Fourier transform infrared spectra, field-emission scanning electron microscopy, transmission electron microscopy, and UC emission spectra, respectively. Highly crystalline cubic phase CaF2:Yb3+,Er3+ nanoparticles are uniformly distributed with an average diameter of about 40–50 nm, and the formation process is also demonstrated. The UC fluorescence has been realized in the as-prepared CaF2:Yb3+,Er3+ nanoparticles on 980-nm excitation. The UC emission transitions for 4F9/2–4I15/2 (red), 2H11/2–4I15/2 (green), 4S3/2–4I15/2 (green), and 2H9/2–4I15/2 (violet) in the Yb3+/Er3+ codoped CaF2 nanoparticles depending on pumping power and temperature have been discussed. The UC mechanism, especially the origin on the temperature-dependent UC emission intensities ratio between 2H11/2 and 4S3/2 levels, have been proposed.


2008 ◽  
Vol 1126 ◽  
Author(s):  
Aravind Suresh ◽  
Joysurya Basu ◽  
Nigel M Sammes ◽  
Barry C Carter ◽  
Benjamin A Wilhite

AbstractBaCe0.25Zr0.60Co0.15O3-x (BCZC) was synthesized via oxalate co-precipitation route. Material was characterized by X-ray diffraction (XRD) and transmission electron microscopy (TEM). Catalytic activity of BCZC with respect to hydrogen generation via methanol partial oxidation was determined. Conductivity of the material at different temperatures and under different environments was determined by AC impedance spectroscopy. XRD and TEM results indicated that BCZC was synthesized as a homogeneous cubic phase material. Catalyst tests indicated that BCZC was catalytically active towards hydrogen generation and AC impedance results were positive enough to warrant further electrochemical studies.


2009 ◽  
Vol 24 (8) ◽  
pp. 2584-2588 ◽  
Author(s):  
Jae Seok Lee ◽  
Se Jin Kim ◽  
Tae Kon Kim ◽  
Rajiv K. Singh ◽  
Madhav B. Ranade

Y2O3:Eu3+ nanophosphor was synthesized by flame spray pyrolysis (FSP) from urea added nitrate based liquid precursor. In this study, urea serves as fuel and subsequently provides additional heat in the flame zone during the synthesis of phosphor particles. The end product shows cubic phase Y2O3:Eu3+ nanophosphor successfully prepared by FSP without heat treatment. The influence of synthesis conditions such as different mol of urea and nitrate source materials in aqueous solution, and doping concentration on luminescent properties, were investigated. The characteristics of nanophosphor such as crystallinity and morphology under various experiments of conditions were carried out by x-ray diffraction (XRD) and field emission-scanning electron microscopy (FE-SEM). The particle size of product was found to be in the range of 20–30 nm from transmission electron microscopy (TEM). In photoluminescence (PL) properties, Y2O3:Eu3+ nanophosphor emitted red light with a peak wavelength of 609 nm when excited with 398 nm wavelength photons.


2008 ◽  
Vol 587-588 ◽  
pp. 931-935
Author(s):  
Priscila Gonçalves ◽  
Filipe M. Figueiredo

The production of La0.95Sr0.05Ga0.90Mg0.10O3-δ powders was achieved at room temperature by a mechanosynthesis route in a high energy planetary ball mill starting from a mixture of lanthanum, strontium, gallium and magnesium oxides. The milling was carried out in nylon containers, using zirconia balls and a balls:powder mass ratio of 10:1. The planetary rotation was kept constant at 650 rotations per minute (rpm), and the container at 1300 rpm, in the opposite direction. The formation of the perovskite phase was detected from the early milling stages and nearly completed after milling for 360 min, as shown by powder X-ray diffraction. Transmission electron microscopy results revealed that powders consist of agglomerates of homogeneous, crystalline particles with an average equivalent diameter of about 16-17 nm, in excellent agreement with average crystallite size estimates obtained from X-ray diffraction.


1999 ◽  
Vol 602 ◽  
Author(s):  
R. Maier ◽  
J. L. Cohn ◽  
J. J. Neumeier ◽  
L. A. Bendersky

AbstractThe properties of a new cubic perovskite phase of thin-film BaFexTi1−xO3 (0.5 ≤x≤0.75) are reported. This material is novel because the corresponding bulk compounds have hexagonal structure for comparable x. The films, grown by pulsed laser deposition on MgO and SrTiO3 substrates, are magnetic (ferro- or ferri-, with Tc > 500°C) and ferroelectric (Tc ∼ 200-300°C).


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