LARGE-SCALE SYNTHESIS OF UNIFORM SILVER BROMIDE NANOWIRES USING ION TRACK MEMBRANE AS TEMPLATE

2010 ◽  
Vol 03 (04) ◽  
pp. 259-262
Author(s):  
SANJEEV KUMAR ◽  
VIJAY KUMAR

Silver bromide (AgBr) nanowires were grown in the pores of ion track membrane. Simple chemical reaction technique was used where pores in the membrane act as reactors. Uniform morphology of nanowires was found using scanning electron microscopy (SEM). An X-ray diffraction (XRD) study shows the crystalline structure. Energy dispersive X-ray fluorescence (EDXRF) technique was used to study the composition of AgBr nanowires. Optical band gap of AgBr nanowires determined using absorption spectra was found to be higher than the bulk.

2021 ◽  
Vol 19 (11) ◽  
pp. 66-71
Author(s):  
Maithm A. Obaid ◽  
Suha A Fadaam ◽  
Osama S. Hashim

The aim of this study is to prepare gold nanoparticles by a simple chemical method at a temperature of 70°C. The solution was dried on glass basest by Casting method, the rate of five drops per sample At a temperature 100 C. Then the structural and optical properties have been confirmed by X-ray diffraction, scanning electron microscopy (SEM) and Transmission Electron microscope (TEM), Fourier Transform Infrared Spectroscopy (FTIR) and spectrum.


2018 ◽  
Vol 29 (1) ◽  
pp. 168
Author(s):  
Tunis Balassim Hassan

Pure and Nickel oxide doped chromium (III) oxide (Cr2O3) nanoparticals are synthesized by hydrothermal technique. The effect of dopant Ni concentration on the structural behavior of Cr2O3 nanoparticles was examined by X-ray diffraction. The average crystallite size of the synthesized nanoparticles was measured from XRD patterns using Scherrer equation and was decreased from 22nm to 12.9 nm with the increasing Nio concentration in Cr2O3 from (0, 0.01, 0.06, and 0.10). Morphologies and compositional elements of the synthesized nanoparticles were observed by the field emission scanning electron microscopy (FESEM) and energy dispersive X-ray (EDX) spectroscopy, respectively. The optical property of the samples was measured by ultraviolet - visible (UV-Vis.) absorption spectroscopy. The observed optical band gap value ranges from 2.3eV to 2.5eV for Ni doped nanoparticles


2016 ◽  
Vol 19 (1) ◽  
pp. 015-019 ◽  
Author(s):  
Jebadurai Joy Jeba Vijila ◽  
Kannusamy Mohanraj ◽  
Sethuramachandran Thanikaikarasan ◽  
Ganesan Sivakumar ◽  
Thaiyan Mahalingam ◽  
...  

Thin films of CuSbS2 have been deposited on ultrasonically cleaned glass substrates using a simple chemical bath deposition technique. Prepared films have been characterized using X-ray diffraction, Field Emission Scanning Electron Microscopy and UV-Vis-NIR spectroscopic techniques, respectively. X-ray diffraction analysis revealed that the prepared films possess polycrystalline in nature with orthorhombic CuSbS2 in addition to secondary phase of monoclinic Cu3SbS3 and cubic Cu12Sb4S13 for different copper concentrations. Field Emission Scanning Electron Spectroscopic analysis showed that the prepared films possess spherical shaped grains with irregular shaped clusters. Optical absorption analysis showed that the prepared films possess band gap value in the range between 1.7 and 2.4 eV.


2011 ◽  
Vol 364 ◽  
pp. 500-503 ◽  
Author(s):  
S. J. Kasim ◽  
F. H. Khaleel ◽  
F. A. Kasim ◽  
M.A. Mahdi

Ag2S nanorods and nonoparticles have been successfully prepared using chemical method. Silver nitrate with molar concentration of 0.1 M and thiourea with different molar concentration were used as a source of Ag++and S++ions, respectively. The pH of solution was in range of 10-11. Scanning electron microscopy (SEM) image showed that the nanorods length and diameter were 2.5-3 μm and 300-400 nm, respectively. X-ray diffraction results showed a monoclinic α-Ag2S phase was obtained. The atomic ratio of silver and sulphur were found using energy dispersive spectroscopy (EDS) and it was 62.39% and 37.61%, respectively.


2021 ◽  
Vol 22 (3) ◽  
pp. 595-601
Author(s):  
R.G. Abaszade ◽  
S.A. Mamedova ◽  
F.G. Agayev ◽  
S.I. Budzulyak ◽  
O.A. Kapush ◽  
...  

We have synthesized large scale, thin, transparent graphene oxide (GO) flakes by Hummer’s method and investigated their suitability for fabrication of transparent nanocomposites. The GO flakes were comprehensively characterized by X-ray diffraction, Scanning Electron Microscopy (SEM), Energy Dispersive X-ray analysis (EDX), Raman spectroscopy and Differential Scanning Calorimetry (DSC). X-ray diffraction displayed the peak of graphene oxide at 9°degree, which is characteristic peak of GO in agreement with the literature results. Scanning Electron Microscopy images revealed that thin, transparent, flake form GO with 14,8 µm lateral size and 0,31µm thickness were synthesized. The comparison with literature results show that for the first time, our group could synthesize large scale, thin and more transparent GO flakes by simple Hummer’s method using simple dispersed graphite. EDX measurements indicate the formation of layered structure with oxygen containing functional groups. The intensity ratio between D and G peaks in the Raman spectra proves that less defective GO flakes have been synthesized. The solution ability of the synthesized material indicate that high quality GO flakes were synthesized, which make them effective soluble material due to oxygen containing groups formed on the graphene plane during synthesis process.DSC results shows that these flakes are thermally stable till 200°C.  Due to high solubility properties, large scale and transparency they can be very useful in fabrication of high optical transparent nanocompoties for replacement indium tin oxide transparent conductors in solar panels, biomedical applications and microwave absorbers for electromagnetic interference (EMI) environmental protection.


2020 ◽  
Vol 31 (8) ◽  
pp. 1367-1384 ◽  
Author(s):  
C Karthikeyan ◽  
R Dhilip Kumar ◽  
J Anandha Raj ◽  
S Karuppuchamy

Metal sulfides received key interest as an electrode material for storage and conversion of energy. Here, the novel nanostructured N17S18 and (CoNi)3S4 materials were synthesized via one-step hydrothermal method, and the synergistic effect of metal ions and electrochemical properties was investigated. A new and simple solution growth technique was employed in this work. The prepared nanopowders were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy, energy-dispersive X-ray spectroscopy techniques. The X-ray diffraction analysis of the prepared nanopowder revealed the formation of cubic phase cobalt nickel sulfides (CoNi)3S4 and hexagonal phase nickel sulfides (Ni17S18). Scanning electron microscopy analysis display fibrous, flakes and sheet-like morphology for CoxSx, N17S18 and (CoNi)3S4, respectively. Fibrous and sheet-like morphology exhibits higher electrochemical performance in supercapacitors. The electrochemical behavior of the amorphous CoxSx, crystallite Ni17S18 and (CoNi)3S4 modified electrodes was investigated using electrochemical impedance spectroscopy, cyclic voltammetry and galvanostatic charge–discharge techniques. The specific capacitance of 57 F/g and 31 F/g were obtained for the amorphous CoxSx and crystalline (CoNi)3S4 powder, respectively. Amorphous CoxSx modified electrode retains 76% of initial capacitance after 1000 repeated cycling process. These results of this study suggest that the CoxSx and crystalline (CoNi)3S4 are appropriate materials for supercapacitor applications.


2011 ◽  
Vol 295-297 ◽  
pp. 1548-1553
Author(s):  
Zhi Yong Jia

The single-crystalline nanobelts of monoclinic Ni(SO4)0.3(OH)1.4have been synthesized on a large scale through a convenient, low-temperature hydrothermal method. The influences of reaction time, pH value, concentration of ammonia on the phase and shape evolution of nanobelts were systematically investigated. It was found that the initial layered Ni(OH)2 thin films as intermediates could be split and converted into the monoclinic Ni(SO4)0.3(OH)1.4nanobelts through SO42-ions inserting process. The formation mechanism of nanobelts involved in the inserting process and the corresponding drive force have been investigated in detail by means of X-ray diffraction (XRD), and scanning electron microscopy (SEM), FT-IR spectra and pH value analyses. In addition to, we have also found that the ammonia molecules acted as both weak base and ligand agent was crucial to the controlling nucleation and inserting process in the formation process of nanobelts.


2016 ◽  
Vol 850 ◽  
pp. 742-747
Author(s):  
Xiang Zhang ◽  
Ping Yun Li ◽  
Xiao De Guo ◽  
Ting Yan

Ultrafine alumina powders were synthesized through pyrocatechol and resorcinol mediated sol-gel process. Aluminum nitrate was applied as the Al source and PVP was the dispersant. X-ray diffraction (XRD) study displayed that γ-Al2O3 powders formed in the range of 800-900 °C, and then γ-Al2O3 transformed to α-Al2O3 at higher temperatures, pure α-Al2O3 powders could be obtained at 1000 °C by using resorcinol as organic monomer. The results of transmission electron microscopy (TEM) revealed that Al2O3 nanoparticles with γ crystalline phase had grain sizes in the range of 5-40 nm. Scanning electron microscopy (SEM) observation displayed that the morphology of the prepared α-Al2O3 powders had aggregated bodies formed by Al2O3 grains in the range of 0.2-0.5μm. These results provide a new way of preparation of alumina powders.


Author(s):  
Л.Н. Маскаева ◽  
Е.А. Федорова ◽  
В.Ф. Марков ◽  
М.В. Кузнецов ◽  
О.А. Липина ◽  
...  

AbstractThe systematized results of studies of the composition, morphology, structure, optical properties, and conductivity of hydrochemically deposited copper(I) selenide thin films (Cu_1.8Se) with the thickness of 390–400 nm are reported. The studies are carried out using scanning electron microscopy, energy-dispersive analysis, X-ray diffraction analysis, and X-ray photoelectron spectroscopy. The hole conductivity of the layers is established by the thermopower technique. The optical band gap determined from the results of studies of optical absorbance and diffuse reflection spectra of the films at 298 K is 2.5 and 1.84 eV for direct and indirect optical transitions, respectively.


2020 ◽  
Vol 1008 ◽  
pp. 104-113
Author(s):  
Huda Khalil ◽  
Abdelhady Kashyout ◽  
Osama Hemeda ◽  
Talaat Meaz

The addition of metal nanoparticles in the Bi-based superconductors has shown the disorder produced by the cations incorporation in the crystal structure affects the TC (Critical temperature) of the system. the addition of new mixture of (Cr2O3: SnO)x on high temperature superconductors HTS Bi1.6Pb0.4 Sr2Ca2Cu3O10+δ (Bi-2223) with ratio 1:1 where x = 0.0, 0.05, 0.10, 0.15 and 0.20 was investigated by solid-state reaction technique was used to prepare superconductor samples. Samples were characterized by X-Ray Diffraction (XRD), Field Emission Scanning Electron Microscopy (FS-EM), Energy Dispersive X-ray (EDX), and electrical resistivity. the results of XRD proved that the structure of 2223 remains the same even with the addition of (Cr2O3: SnO)x nanoparticles. The phase 2223 has the majority even phase Bi-2212 and phase Ca2PbO4 showed a contribution inside structure. As a result of the change physico-chemical properties resistivity of the doped optimized sample x = 0.10 was increasing 2.2 K approximately rather than the undoped one then decreased gradually up to x = 0.20. From resistivity measurement, the TC of 2223 doped with (Cr2O3: SnO)x at x = 0.10 was 113.2 K approximately. The addition of metal oxides in superconductor materials has been considered to be one of the most promising materials for large scale applications in superconducting industry.


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