The effect of induced strains on the optical band gaps in lanthanum-doped zinc ferrite nanocrystalline powders

2016 ◽  
Vol 30 (18) ◽  
pp. 1650230 ◽  
Author(s):  
Fathalla Hamed ◽  
Tholkappiyan Ramachandran ◽  
Vishista Kurapati

ZnFe[Formula: see text]La[Formula: see text]O4 nanocrystalline powders were synthesized by auto-combustion with the aid of glycine as fuel. The synthesized powders were subjected to heat treatment in air at constant temperatures (600–970[Formula: see text]C) for a period of 2 h. The annealed powders were characterized by X-ray diffraction (XRD), Fourier transformation infrared spectroscopy (FTIR), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS) and UV–Vis–NIR spectroscopy. The as-synthesized and annealed powders formed spongy porous network structure with voids and pores. All the powders were found to be single phase nanomaterial with cubic spinel crystal structure and the desired composition; however, they contained strains, dislocations and lattice distortions. Some of these strains and dislocations are relaxed as a function of annealing temperature. The powders displayed direct and indirect optical band gaps. The energies of these band gaps were found to vary as a function of the induced strains and dislocations. It is suggested that the energy of the optical band gap in lanthanum-doped zinc ferrite nanocrystalline powders can be varied as a function of induced strains if the initial preparation conditions and the following heat treatments are controlled.

2006 ◽  
Vol 11-12 ◽  
pp. 159-162 ◽  
Author(s):  
Yong Ge Cao ◽  
Lei Miao ◽  
Sakae Tanemura ◽  
Yasuhiko Hayashi ◽  
Masaki Tanemura

Transparent indium-doped ZnO (IZO) films with low In content (<6at%) were fabricated through radio-frequency (rf) helicon magnetron sputtering. Formation of In-Zn-O solid solution was confirmed by X-ray diffraction (XRD) patterns. Incorporation of indium into ZnO films enhances the optical transmission in the visible wavelength. The optical band-gaps slightly increase from 3.25eV (ZnO) to 3.28eV (In0.04Zn0.96O) and to 3.30eV (In0.06Zn0.94O) due to Burstain-Moss effect. The Urbach tail parameter E0, which is believed to be a function of structural disorder, increases from 79meV (ZnO), to 146meV (In0.04Zn0.96O), and to 173meV (In0.06Zn0.94O), which is consistent with increase of Full-Width Half-Maximum (FWHM) in corresponding XRD patterns. Decreasing in crystal quality with increasing indium concentration is also confirmed by photoluminescence spectra.


2022 ◽  
Vol 0 (0) ◽  
Author(s):  
Zein K. Heiba ◽  
Mohamed Bakr Mohamed ◽  
Noura M. Farag ◽  
Ali Badawi

Abstract (1−x)CuCo2O4/xMnS (x = 0, 0.25, 0.5) nanocomposite samples were formed using hydrothermal and thermolysis procedures. X-ray diffraction (XRD) phase analysis showed the formation of only CuCo2O4 phase necessitating the inclusion of Mn and S ions into the CuCo2O4 lattice. Fourier-transform infrared spectroscopy (FTIR) analyses confirmed the presence of Mn and S ions in the nanocomposite samples. Rietveld refinement method was applied to determine the cation distribution of the different ions between different sites. The cell parameter (a) has no fixed trend of change. The average crystallite size is almost the same for all samples with an average of 15 nm. The effect of insertion of Mn and S ions into the CuCo2O4 on the diffused absorbance, extinction coefficient, refractive index, dielectric properties, and nonlinear optical parameters was discussed in detail. The pristine CuCo2O4 nanoparticles have two direct optical band gaps (1.65, 2.74) eV which are decreased to (1.59, 2.56) and (1.58, 2.54) eV for the MnS content x = 0.25 and 0.5, respectively. The two indirect optical band gaps of pristine CuCo2O4 changed irregularly as the MnS amount increased in the nanocomposite. The PL spectrum of CuCo2O4 is shifted to higher wavelength in the visible region upon alloying with MnS. The photoluminescence (PL) intensity of the nanocomposite samples is smaller than that of CuCo2O4 sample. The emitted PL colors depended on the amount of Mn and S ions in the CuCo2O4 matrix.


2012 ◽  
Vol 463-464 ◽  
pp. 1052-1056
Author(s):  
Ai Xiang Zeng ◽  
Jun Yuan

Ni0.6-xZn0.4MgxFe2O4were synthesized by sol-gel auto-combustion method with Zn(NO3.) 2 •6H2O. , Ni(NO3.) )2•6H2O. , Mg(NO3.) )2•6H2O. , Fe(NO3.) )3•9H2O. , COOO2. and NH3•H2O. X-ray diffraction (XRD) analysises show that the sample is single phase and the doping of magnesium makes no difference to nickel-zinc ferrite’s crystal structure; nickel-zinc ferrite has formed after auto-combustion. Scanning electron microscope analysises show that after sintered the sample’s size is more even and the doping of magnesium makes the size smaller and more even too.


2010 ◽  
Vol 152-153 ◽  
pp. 63-66
Author(s):  
Shi Yin Li ◽  
Zhen Ni Du ◽  
Yong Cai Zhang

A novel template-free method, which was based on heating the mixture of InCl3•4H2O and thiourea in air from room temperature to 200 or 250 °C, coupled with a subsequent washing treatment using distilled water and ethanol, was proposed for the synthesis of In2S3 hierarchical nanostructure. X-ray diffraction and field emission scanning electronic microscopy demonstrated that the obtained products were pure cubic phase In2S3 urchin-like clusters built up by mainly nanoflakes (about 12–47 nm thick). UV-vis absorption spectra disclosed that the as-prepared In2S3 urchins had optical band gaps in the range of about 2.18–2.26 eV.


Author(s):  
U. Aebi ◽  
R. Millonig ◽  
H. Salvo

To date, most 3-D reconstructions of undecorated actin filaments have been obtained from actin filament paracrystal data (for refs, see 1,2). However, due to the fact that (a) the paracrystals may be several filament layers thick, and (b) adjacent filaments may sustantially interdigitate, these reconstructions may be subject to significant artifacts. None of these reconstructions has permitted unambiguous tracing or orientation of the actin subunits within the filament. Furthermore, measured values for the maximal filament diameter both determined by EM and by X-ray diffraction analysis, vary between 6 and 10 nm. Obviously, the apparent diameter of the actin filament revealed in the EM will critically depend on specimen preparation, since it is a rather flexible supramolecular assembly which can easily be bent or distorted. To resolve some of these ambiguities, we have explored specimen preparation conditions which may preserve single filaments sufficiently straight and helically ordered to be suitable for single filament 3-D reconstructions, possibly revealing molecular detail.


Cerâmica ◽  
2019 ◽  
Vol 65 (374) ◽  
pp. 274-281 ◽  
Author(s):  
S. S. Satpute ◽  
S. R. Wadgane ◽  
S. R. Kadam ◽  
D. R. Mane ◽  
R. H. Kadam

Abstract Y3+ substituted strontium hexaferrites having chemical composition SrYxFe12-xO19 (x= 0.0, 0.5, 1.0, 1.5) were successfully synthesized by sol-gel auto-combustion method. The structural and morphological studies of prepared samples were investigated by using X-ray diffraction technique, energy dispersive X-ray spectroscopy, field emission scanning electron microscopy (FE-SEM) and high-resolution transmission electron microscopy. The X-ray diffraction pattern confirmed the single-phase hexagonal structure of yttrium substituted strontium ferrite and the lattice parameters a and c increased with the substitution of Y3+ ions. The crystallite size also varied with x content from 60 to 80 nm. The morphology was studied by FE-SEM, and the grain size of nanoparticles ranged from 44 to 130 nm. The magnetic properties were investigated by using vibrating sample magnetometer. The value of saturation magnetization decreased from 49.60 to 35.40 emu/g. The dielectric constant decreased non-linearly whereas the electrical dc resistivity increased with the yttrium concentration in strontium hexaferrite.


2020 ◽  
Vol 43 (1) ◽  
pp. 26-42 ◽  
Author(s):  
Zahra Hajian Karahroudi ◽  
Kambiz Hedayati ◽  
Mojtaba Goodarzi

AbstractThis study presents a preparation of SrFe12O19– SrTiO3 nanocomposite synthesis via the green auto-combustion method. At first, SrFe12O19 nanoparticles were synthesized as a core and then, SrTiO3 nanoparticles were prepared as a shell for it to manufacture SrFe12O19–SrTiO3 nanocomposite. A novel sol-gel auto-combustion green synthesis method has been used with lemon juice as a capping agent. The prepared SrFe12O19–SrTiO3 nanocomposites were characterized by using several techniques to characterize their structural, morphological and magnetic properties. The crystal structures of the nanocomposite were investigated via X-ray diffraction (XRD). The morphology of SrFe12O19– SrTiO3 nanocomposite was studied by using a scanning electron microscope (SEM). The elemental composition of the materials was analyzed by an energy-dispersive X-ray (EDX). Magnetic properties and hysteresis loop of nanopowder were characterized via vibrating sample magnetometer (VSM) in the room temperature. Fourier transform infrared spectroscopy (FTIR) spectra of the samples showed the molecular bands of nanoparticles. Also, the photocatalytic behavior of nanocomposites has been checked by the degradation of azo dyes under irradiation of ultraviolet light.


Author(s):  
Nesrine Jaouabi ◽  
Wala Medfai ◽  
Marouan Khalifa ◽  
Rabia Zaghouani ◽  
Hatem Ezzaouia

The titanium dioxide (TiO2) purity is very important for the TiO2-based applications making essential the impurities density reduction. In this study, we propose an efficient purification process of TiO2 powder in order to reduce impurities. The low-cost proposed approach is based on an iterative gettering (IG) process combining three main steps: (1) a porous TiO2 sacrificial layer formation (p-TiO2), (2) a rapid thermal annealing (RTA) of p-TiO2 powder in an infrared oven at 950°C under air permitting the residual impurities diffusion to the porous layer surface and (3) etching in acid solution to remove the porous layer. Effect of the proposed gettering process on purification efficiency was evaluated by different characterization techniques such as the transmission electron microscopy (TEM), the energy dispersive x-ray spectroscopy (EDX), the UV–Visible-NIR spectroscopy, the X-ray diffraction (XRD) and atomic absorption spectroscopy (AAS). The obtained results showed the efficient removal of metal impurities, such as Cu, Al, P, and Fe confirming the efficiency of the process improving the purity from 89% to 99.96%.


2013 ◽  
Vol 665 ◽  
pp. 254-262 ◽  
Author(s):  
J.R. Rathod ◽  
Haresh S. Patel ◽  
K.D. Patel ◽  
V.M. Pathak

Group II-VI compounds have been investigated largely in last two decades due to their interesting optoelectronic properties. ZnTe, a member of this family, possesses a bandgap around 2.26eV. This material is now a day investigated in thin film form due to its potential towards various viable applications. In this paper, the authors report their investigations on the preparation of ZnTe thin films using vacuum evaporation technique and their structural and optical characterizations. The structural characterization, carried out using an X-ray diffraction (XRD) technique shows that ZnTe used in present case possesses a cubic structure. Using the same data, the micro strain and dislocation density were evaluated and found to be around 1.465×10-3lines-m2and 1.639×1015lines/m2respecctively. The optical characterization carried out in UV-VIS-NIR region reveals the fact that band gap of ZnTe is around 2.2eV in present case. In addition to this, it was observed that the value of bandgap decreases as the thickness of films increases. The direct transitions of the carries are involved in ZnTe. Using the data of UV-VIS-NIR spectroscopy, the transmission coefficient and extinction coefficient were also calculated for ZnTe thin films. Besides, the variation of extinction coefficient with wavelength has also been discussed here.


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