The lattice parameter of nanocrystalline Ni as function of crystallite size

2011 ◽  
Vol 43 (6) ◽  
pp. 1155-1161 ◽  
Author(s):  
J. Sheng ◽  
G. Rane ◽  
U. Welzel ◽  
E.J. Mittemeijer
Keyword(s):  
Crystallite Size ◽  
Lattice Parameter

Effect of the structural changes on the mechanical properties of the sintered films

2016 ◽  
Vol 12 (1) ◽  
pp. 4141-4144
Author(s):  
Garima Jain
Keyword(s):  
Crystallite Size ◽  
Lattice Constant ◽  
Structural Changes ◽  
Structural Investigation ◽  
Energy Gap ◽  
Lattice Parameter ◽  
Metal Chalcogenides ◽  
Optical Energy Gap ◽  
Tin Telluride ◽  
Physical Quantities

Polycrystalline films of tin telluride were prepared by sintering technique. The structural investigation of the films with different thicknesses enables to determine lattice parameter, crystallite size and strain existing in the films. The XRD traces showed that strain was tensile in nature. The crystallite size increases with thickness while strain decreases. Higher the value of tensile strain, larger is the lattice constant. The optical energy gap shows a descending nature with increasing strain and so with the lattice constant. Such an attempt made to delve into interdependence of basic physical quantities helps to explore the properties of SnTe and utilize it as an alternative to heavy metal chalcogenides in various technological applications.  

scholarly journals Measurements by x-ray diffraction of the temperature dependence of lattice parameter and crystallite size for isostatically-pressed graphite

Carbon Trends ◽  
2021 ◽  
pp. 100071
Author(s):  
Keith R. Hallam ◽  
James Edward Darnbrough ◽  
Charilaos Paraskevoulakos ◽  
Peter J. Heard ◽  
T. James Marrow ◽  
...  
Keyword(s):  
Temperature Dependence ◽  
Crystallite Size ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
X Ray

Synthesis of ZrO2–Y6WO12 solid solution powders by a polymerized complex method

1998 ◽  
Vol 13 (4) ◽  
pp. 939-943 ◽  
Author(s):  
Junfeng Ma ◽  
Masahiro Yoshimura ◽  
Masato Kakihana ◽  
Masatomo Yashima
Keyword(s):  
Solid Solution ◽  
Crystallite Size ◽  
Surface Area ◽  
Solid Solutions ◽  
Lattice Parameter ◽  
Cubic Phase ◽  
Complex Method ◽  
Amorphous Precursor ◽  
Fine Powders ◽  
Polymerized Complex Method

A series of solid solutions (1 − x) ZrO2 · xY0.857 W0.143 O1.714 (1/7Y6WO12) of metastable cubic phase were synthesized at 800 °C through a polymerized complex method. Lattice parameter a0 of solid solutions varies linearly with Y0.857 W0.143 O1.714 content (x). Crystallization began to occur above 400 °C from amorphous precursor to yield at 800 °C fine powders of 6–10 nm and 19–40 m2/g for crystallite size and surface area, respectively.

scholarly journals Crystal Structures and Magnetic Properties of Polyethylene Glycol (PEG-4000) Encapsulated Co0.5Ni0.5Fe2O4 Magnetic Nanoparticles

2018 ◽  
Vol 8 (2) ◽  
pp. 75
Author(s):  
Edi Suharyadi ◽  
Lintang Griyanika ◽  
Joko Utomo ◽  
Ayu Kurnia Agustina ◽  
Takeshi Kato ◽  
...  
Keyword(s):  
Magnetic Nanoparticles ◽  
Crystallite Size ◽  
Spinel Ferrite ◽  
Lattice Parameter ◽  
X Ray ◽  
Maximum Magnetization ◽  
Peg 4000 ◽  
Significant Difference ◽  
Ray Density ◽  
Xrd Patterns

Nanocrystalline mixed spinel ferrite of Co0.5Ni0.5Fe2O4 magnetic nanoparticles (MNPs) has been successfully synthesized by coprecipitation method and encapsulated by PEG-4000 with various concentrations. X-Ray Diffraction (XRD) patterns showed that nanoparticles contained Co0.5Ni0.5Fe2O4 spinel ferrite with crystallite size of 14.9 nm. After PEG-4000 encapsulation particles size decreased became 7.7 nm. Interaction Co0.5Ni0.5Fe2O4 nanoparticles with long chain PEG-4000 caused the crystal growth trap. Lattice parameter and X-Ray density have no significant difference after encapsulated PEG-4000. The coercivity (𝐻𝑐) of Co0.5Ni0.5Fe2O4 was 214 Oe. The 𝐻𝑐 decreased after PEG-4000 encapsulation became 127 Oe, which is due to the decrease of crystallite size. The maximum magnetization (Mmax) of Co0.5Ni0.5Fe2O4 was 12.0 emu/g, and decreased after PEG-4000 encapsulation to 11.7 emu/g, because PEG-4000 is paramagnetic. After the concentration of PEG-4000 increased, then the amount of paramagnetic material increase which lead maximum magnetization decrease.

scholarly journals Crystallographic, Energy Gap, Photoluminescence and Photo-Catalytic Investigation of Cu Doped Cd0.9Zn0.1S Nanostructures by Co-Precipitation Method

2021 ◽  
Author(s):  
P. Raju ◽  
Joseph Prince Jesuraj ◽  
S. Muthukumaran
Keyword(s):  
Crystallite Size ◽  
Energy Gap ◽  
Wavelength Region ◽  
Lattice Parameter ◽  
Precipitation Method ◽  
Optical Absorbance ◽  
Stability Measurement ◽  
Cubic Structure ◽  
The Stability ◽  
Co Precipitation

Abstract The controlled synthesis of Cd0.9Zn0.1S, Cd0.89Zn0.1Cu0.01S and Cd0.87Zn0.1Cu0.03S nanostructures by simple chemical co-precipitation technique was reported. The XRD investigation confirmed the basic CdS cubic structure on Zn-doped CdS and also Zn, Cu dual doped CdS with no secondary/impurity related phases. No modification in cubic structure was detected during the addition of Zn/Cu into CdS. The reduction of crystallite size from 63 Å to 40 Å and the changes in lattice parameter confirmed the incorporation of Cu into Cd0.9Zn0.1S and generation of Cu related defects. The shift of absorption edge along upper wavelength region and elevated absorption intensity by Cu doping can be accredited to the collective consequence of quantization and the generation of defect associated states. The enhanced optical absorbance and the reduced energy gap recommended that Cd0.87Zn0.1Cu0.03S nanostructure is useful to enhance the efficiency of opto-electronic devices. The presence of Cd-S / Zn-Cd-S /Zn/Cu-Cd-S chemical bonding were confirmed by Fourier transform infrared investigation. The elevated green emissions by Cu incorporation was explained by decrease of crystallite size and creation of more defects. Zn, Cu dual doped CdS nanostructures are recognized as the possible and also efficient photo-catalyst for the removal dyes like methylene blue. The enhanced photo-catalytic behaviour of Zn, Cu dual doped CdS is the collective consequences of high density electron-hole pairs creation, enhanced absorbance in the visible wavelength, surface area enhancement, reduced energy gap and the formation of novel defect associated states. The stability measurement signified that Cu doped Cd0.9Zn0.1S exhibits superior dye removal ability and better stability even after 6 repetitive runs with limited photo-corrosion.

PYROMILLING SYNTHESIS OF NANOCRYSTALLINE TITANIUM CARBIDE

NANO ◽  
2013 ◽  
Vol 08 (02) ◽  
pp. 1350023 ◽  
Author(s):  
M. RAZAVI ◽  
S. ZAMANI ◽  
M. R. RAHIMIPOUR ◽  
P. KHATIBZADEH
Keyword(s):  
Titanium Carbide ◽  
Crystallite Size ◽  
Milling Time ◽  
Raw Materials ◽  
Lattice Parameter ◽  
Stoichiometric Ratio ◽  
Nanocrystalline Titanium ◽  
Standard Value ◽  
Increasing Temperature ◽  
First Time

For the first time, pyromilling synthesis for production of nanocrystalline titanium carbide was presented in this research. Raw materials containing stoichiometric ratio of titanium and carbon were milled and heated simultaneously. Samplings were done at different times. Then, phase transformation, crystallite size and strain of samples were estimated by XRD technique. Microstructures of milled samples were studied by SEM and TEM. Results showed that by increasing temperature, milling time for synthesizing of titanium carbide was reduced. Crystallite size of milled samples were in nanometer scale which were reduced by increasing of milling time and decreasing of temperature while strain was intensified. Existence of created strain changed lattice parameter of synthesized titanium carbide from standard value.

scholarly journals Characterization of Mechanically Alloyed Nanocrystalline Fe(Al): Crystallite Size and Dislocation Density

2010 ◽  
Vol 2010 ◽  
pp. 1-8 ◽  
Author(s):  
M. Mhadhbi ◽  
M. Khitouni ◽  
L. Escoda ◽  
J. J. Suñol ◽  
M. Dammak
Keyword(s):  
Solid Solution ◽  
Dislocation Density ◽  
Crystallite Size ◽  
Average Crystallite Size ◽  
High Energy ◽  
Lattice Parameter ◽  
X Ray Diffraction ◽  
Mechanically Alloyed ◽  
Scanning Calorimetry ◽  
High Energy Ball Mill

A nanostructured disordered Fe(Al) solid solution was obtained from elemental powders of Fe and Al using a high-energy ball mill. The transformations occurring in the material during milling were studied with the use of X-ray diffraction. In addition lattice microstrain, average crystallite size, dislocation density, and the lattice parameter were determined. Scanning electron microscopy (SEM) was employed to examine the morphology of the samples as a function of milling times. Thermal behaviour of the milled powders was examined by differential scanning calorimetry (DSC). The results, as well as dissimilarity between calorimetric curves of the powders after 2 and 20 h of milling, indicated the formation of a nanostructured Fe(Al) solid solution.

scholarly journals Influence of Milling Media on the Mechanical Alloyed W-0.5 wt.% Ti Powder Alloy

2016 ◽  
Vol 2016 ◽  
pp. 1-6 ◽  
Author(s):  
Hadi Jahangiri ◽  
Sultan Sönmez ◽  
M. Lütfi Öveçoğlu
Keyword(s):  
Crystallite Size ◽  
Milling Time ◽  
High Energy ◽  
Lattice Parameter ◽  
Mechanically Alloyed ◽  
High Energy Ball Mill ◽  
Powder Density ◽  
Energy Ball ◽  
Ti Powder ◽  
Milled Powders

The effects of milling atmosphere and mechanical alloying (MA) duration on the effective lattice parameter, crystallite size, lattice strain, and amorphization rate of the W-0.5 wt.% Ti powders were investigated. W-0.5 wt.% Ti powders were mechanically alloyed (MA’d) for 10 h and 20 h in a high energy ball mill. Moreover, morphology of the powders for various MA was analyzed using SEM microscopy. Their powder density was also measured by helium pycnometer. The dry milled agglomerated powders have spherical particle, while wet milled powders have layered morphology. Milling media and increasing of milling time significantly reduce the crystallite size. The smallest crystallite size is 4.93 nm which belonged to the dry milled powders measured by Lorentzian method after 20 hours’ MA. However, after 20 hours, MA’d powders show the biggest crystallite size, as big as 57.07 nm, measured with the same method in ethanol.

In-plane lattice-parameter and crystallite-size determination in a turbostratic graphite-like structure

1994 ◽  
Vol 27 (5) ◽  
pp. 767-771 ◽  
Author(s):  
Yu. G. Andreev ◽  
T. Lunström
Keyword(s):  
Crystallite Size ◽  
Line Shape ◽  
Lattice Parameter ◽  
Size Determination ◽  
Instrumental Function ◽  
Boron Nitrides ◽  
Plane Lattice ◽  
Profile Fitting ◽  
Theoretical Line ◽  
Diffraction Peaks

A detailed recipe is given for the refinement of in-plane lattice-parameter and crystallite-size values of a turbostratic graphite-like structure through the profile fitting of the diffraction peaks from random layers. Folding of the theoretical line shape with the experimentally measured instrumental function provides convenient correction for systematic broadening. The devised technique is applied to the analysis of turbostratic hexagonal boron nitrides.

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