Structural Properties of Al-Cu Thin Films after Heat Treatment

2009 ◽  
Vol 609 ◽  
pp. 87-93
Author(s):  
S. Lallouche ◽  
M.Y. Debili
Keyword(s):  
Heat Treatment ◽  
Grain Size ◽  
Dislocation Density ◽  
Annealing Temperature ◽  
Exothermic Peak ◽  
Thermal Study ◽  
X Ray Diffraction ◽  
X Ray ◽  
Decomposition Behaviour

In this work we are interested by the decomposition behaviour after heat treatment at 500°C of nanostructured Al-Cu deposits, prepared by radio frequency (13.56MHz) magnetron sputtered from composite targets. The use of X-ray diffraction leads to the characterization of different structures and the estimation of grain size and dislocation density. The grain size of the films is found to increase with annealing. The dislocation density is observed to exhibit a decrease trend with annealing temperature which leads to a reduction in the concentration of lattice imperfections A specific thermal study of the Al-Cu deposits, by combined thermal analysis (TDA/TG) permit to follow the structural behavior of the deposits with heat treatment. For Al-7.21at%Cu deposit, the exothermic peak convolution may be due to the elimination of micro deformations present in the sample.

scholarly journals Synthesis and characterization of apatite silicated powders with wet precipitation method

2021 ◽  
Vol 234 ◽  
pp. 00106
Author(s):  
Houda Labjar ◽  
Hassan Chaair
Keyword(s):  
Electron Microscopy ◽  
Heat Treatment ◽  
Analytical Techniques ◽  
Precipitation Method ◽  
Synthesis And Characterization ◽  
X Ray Diffraction ◽  
X Ray ◽  
Wet Precipitation ◽  
Scanning Electron

The synthesis of apatite silicated Ca10(PO4)6-x(SiO4)x(OH)2-x (SiHA) with 0≤x≤2 was investigated using a wet precipitation method followed by heat treatment using calcium carbonate CaCO3 and phosphoric acid H3PO4 and silicon tetraacetate SiC8H20O4 (TEOS) in medium of water ethanol, with three different silicate concentrations. After drying, the samples are ground and then characterized by different analytical techniques like X-ray Diffraction (XRD), Fourier Transform Infrared Spectroscopy (FTIR) and Scanning electron Microscopy (SEM) and chemical analysis.

Synthesis and characterization of MnO2nanowires

2017 ◽  
Vol 31 (02) ◽  
pp. 1750006 ◽  
Author(s):  
Mohammad Hossein Ghorbani ◽  
Abdol Mahmood Davarpanah
Keyword(s):  
Lithium Batteries ◽  
Manganese Oxides ◽  
Room Temperature ◽  
Annealing Temperature ◽  
Sol Gel ◽  
Average Crystallite Size ◽  
X Ray Diffraction ◽  
X Ray ◽  
Xrd Method

Manganese oxides are of more interest to researchers because of their ability as catalysts and lithium batteries. In this research, MnO2nanowires with diameter about 45 nm were synthesized by sol–gel method at room temperature (RT). Effect of increasing the annealing temperature from 400[Formula: see text]C to 600[Formula: see text]C on crystalline structure of nanostructure were studied and average crystallite size was estimated about 22 nm. X-ray Diffraction (XRD) method, Energy-Dispersive X-ray Diffraction (EDXD), Scanning Electron Microscopy (SEM) and Vibrating Sample Magnetometer (VSM) were used to characterize the nanowires of MnO2.

The Effect of Ethanol Solvent on Characterization of MAPbI3 Perovskite

2021 ◽  
Vol 1039 ◽  
pp. 307-312
Author(s):  
Mohammad Malik Abood ◽  
Osama Abdul Azeez Dakhil ◽  
Aref Saleh Baron
Keyword(s):  
Grain Size ◽  
Optical Properties ◽  
Morphological Characteristics ◽  
X Ray Diffraction ◽  
Lead Iodide ◽  
X Ray ◽  
Diffraction Patterns ◽  
Photovoltaic Technologies ◽  
Perovskite Photovoltaic

Methyl ammonium lead iodide CH3NH3PbI3 Perovskite was synthesized by a new method mixing between one and two steps, in addition, the ethanol solvent was used to dissolve CH3NH3I and compared with isopropanol solvent. The characterizations of synthesized perovskite samples included the structural properties, morphological characteristics and optical properties. The intensity and orientation in X-ray diffraction patterns appear clearly in ethanol solvent while disappearing at a peak at 12o due to the speed reaction of perovskite in this solvent. Additionally, the ethanol solvent increasing the grain size of perovskite which homogeneity of the surface morphology. the ethanol solvent cause a decrease in the wavelength of absorbance edge in addition to an increase in the energy bandgap value. Keywords: Ethanol Solvent, Perovskite, Photovoltaic Technologies, X-ray diffraction.

Preparation and Characterization of Zn-Se Bilayer Structure

2007 ◽  
Vol 31 ◽  
pp. 153-157
Author(s):  
M. Singh ◽  
J.S. Arora ◽  
Kamlendra Awasthi ◽  
R. Nathawat ◽  
Y.K. Vijay
Keyword(s):  
Grain Size ◽  
Annealing Temperature ◽  
Hexagonal Structure ◽  
Scattering Data ◽  
Bilayer Structure ◽  
X Ray Diffraction ◽  
Thermal Evaporation Method ◽  
Rutherford Back Scattering ◽  
Back Scattering

The Zn-Se bilayer structure prepared using thermal evaporation method at pressure 10-5 Torr. These films annealed in the vacuum for two hours on different constant temperatures. The optical band gap was found to be varying with annealing temperature due to removal of defects and increase in grain size. It was also observed by the X-ray diffraction pattern the grain size of the film increase with annealing temperature. The lattice constant of hexagonal structure of these films is found to be a =b=4.42Å and c=5.68Å. The dominant peaks to be at 23.2°,28° and 43.9° having values (100), (002) and (111) respectively. The Rutherford back scattering data of these films confirmed the mixing of elements with time.

Characterization of aluminosilicate (mullite) precursors prepared by a mechanochemical process

1998 ◽  
Vol 13 (8) ◽  
pp. 2184-2189 ◽  
Author(s):  
J. Temuujin ◽  
K. Okada ◽  
K. J. D. MacKenzie
Keyword(s):  
Heat Treatment ◽  
Nmr Spectra ◽  
Spinel Phase ◽  
Mas Nmr ◽  
X Ray Diffraction ◽  
Hydrated Alumina ◽  
X Ray ◽  
New Si ◽  
Grinding Time

Aluminosilicate precursors were prepared by mechanochemical treatment of gibbsitesilica gel mixtures. The effect of grinding on their structure and thermal behavior has been examined by 27Al and 29Si MAS NMR, x-ray diffraction (XRD), differential thermal analysis-thermogravimetry (DTA-TG), and Fourier transform infrared (FTIR). After 8 h grinding, the hydrated alumina was completely changed to an amorphous phase which showed a new exothermic DTA peak at about 980 °C due to the formation of γ–Al2O3 or spinel phase. This behavior was related to changes in the Al and Si environments, as deduced from the MAS NMR spectra. With increased grinding time, some 4-coordinated Al appears, together with an Al resonance at about 30 ppm. Simultaneously, a new Si resonance appears at about −90 ppm, indicating a greater degree of homogeneity in the ground samples. Mullite crystallizes at 1200 °C from samples ground for 8–20 h, its XRD intensity increasing with increased milling times, in agreement with the NMR, DTA, and FTIR data. Changes in the Al and Si environments during heat treatment, as reflected by the NMR spectra, are also reported.

Characterization of edge dislocation density through X-ray diffraction rocking curves

2020 ◽  
Vol 551 ◽  
pp. 125893
Author(s):  
Yangfeng Li ◽  
Shen Yan ◽  
Xiaotao Hu ◽  
Yimeng Song ◽  
Zhen Deng ◽  
...  
Keyword(s):  
Dislocation Density ◽  
Edge Dislocation ◽  
X Ray Diffraction ◽  
X Ray

Mechanical Properties of Porous Nanophase Materials Measured by Instrumental Indentation

1995 ◽  
Vol 400 ◽  
Author(s):  
H. Van Swygenhoven ◽  
W. Wagner ◽  
J. Löffler
Keyword(s):  
Mechanical Properties ◽  
Grain Size ◽  
Annealing Temperature ◽  
X Ray Diffraction ◽  
X Ray ◽  
Gas Condensation ◽  
Mean Grain Size ◽  
Nanophase Materials ◽  
The Mean ◽  
Instrumental Indentation

AbstractMechanical properties of nanostructured intermetallic Ni3Al synthesized by the inert-gas condensation technique are studied by means of instrumental indentation using the ICT-CSEMEX indenter. This instrument is a microindenter which continously measures load and displacement. Load-displacement curves are performed as function of grain size, consolidation- and annealing temperature. The mean grain size of the samples are studied by means of x-ray diffraction and small-angle neutron scattering.

Neodymium Incorporation in Zirconolite-Based Glass-Ceramics

2000 ◽  
Vol 663 ◽  
Author(s):  
P. Loiseau ◽  
D. Caurant ◽  
N. Baffier ◽  
C. Fillet
Keyword(s):  
Heat Treatment ◽  
Glass Ceramics ◽  
Fission Products ◽  
Treatment Temperature ◽  
Spent Fuel ◽  
X Ray Diffraction ◽  
Parent Glass ◽  
X Ray ◽  
Spin Resonance

ABSTRACTThe investigations on enhanced reprocessing of nuclear spent fuel, and notably on separating the long-lived minor actinides, such as Am and Cm, from the other fission products have led to the development of highly durable specific matrices such as glass-ceramics for their immobilization. This study deals with the characterization of zirconolite (CaZrTi2O7) based glass-ceramics synthesized by devitrification of an aluminosilicate parent glass. Trivalent actinide ions were simulated by neodymium, which is a paramagnetic local probe. Glass-ceramics with Nd2O3 contents ranging from 0 to 10 weight % were prepared by heat treatment of a parent glass at two different growth temperatures: 1050° and 1200°C. X-ray diffraction (XRD), energy dispersive X-ray analysis (EDX) and electron spin resonance (ESR) measurements clearly indicate that Nd3+ ions are partly incorporated in zirconolite crystals formed in the bulk of the glass-ceramic samples. The amount of neodymium in the crystalline phase was estimated using ESR results and was found to decrease with increasing either heat treatment temperature or total Nd2O3 content.

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