Synthesis and Characterization of the Nano Semiconducting Material Cadmium Sulphide

2011 ◽  
Vol 699 ◽  
pp. 79-88
Author(s):  
S. Santhosh Kumar Jacob ◽  
Saravananakumar S. ◽  
R. Saravanan

In this work, CdS nano particles were synthesized using aqueous precipitation method; This method is simple, fast and can be carried out at room temperature. Various techniques like X-ray powder diffraction and UV-visible absorption spectroscopy are used for the structural characterization like electron density distribution and estimation of inter atomic distances between the atoms of the nano particles. The optical band gap of this material has been determined in order to establish a relationship between energy gap of bulk and nano materials.

2013 ◽  
Vol 2013 ◽  
pp. 1-6 ◽  
Author(s):  
Narongrit Tipcompor ◽  
Somchai Thongtem ◽  
Titipun Thongtem

Cubic AgSbS2nanostructured flowers of nanorods were successfully synthesized by microwave-assisted refluxing of AgNO3, Sb(CH3COO)3, and L-cysteine (C3H7NO2S) dissolved in ethylene glycol at the pH of 4, characterized by X-ray diffraction (XRD) and electron microscopy (EM). The 1.89 eV direct energy gap was determined by UV-visible absorption, including two 688 and 857 nm emission wavelengths by photoluminescence (PL) spectroscopy. A possible formation mechanism of AgSbS2nanostructured flowers was also proposed according to the experimental results.


2021 ◽  
Author(s):  
Nejeh Hannachi ◽  
Thierry ROISNEL ◽  
Faouzi HLEL

Abstract A new non-centrosymmetricorganotin (IV) hybrid compoundC5H14N2 [SnCl6] 2H2O was determined by single crystal X-ray diffraction at 150(2) K. Its crystal structure was solved by single crystal X-ray diffraction reveling that compound crystallizes in the orthorhombic system with Pbca space group with the following lattice parameters: a = 12.1486 (15) Å, b= 15.4571 (17) Å, c = 16.7610 (18) Å with Z = 8. The bonding between inorganic and organic entities in the compounds is realized by hydrogen bonding O−H…O ,O−H…Cl , NH • • • Cl, N-H…Cl and O−H…Cl. Finally,UV-visible absorption measurements exhibit two absorption bands (226 nm and 262 nm).The optical band gap (Eg) is deduced to be 3.46 Ev.


2020 ◽  
Vol 3 (1) ◽  
Author(s):  
Gowri Manohari N ◽  
Mohanapriya N

In this present study, Iron Oxide nano particles were synthesized by using Green method. For this synthesis on Iron oxide, the leaf extract of piper betle was used as a reducing agent and FeCl3 as a precursor. Thus, they were characterized by XRD, SEM,EDX and FTIR. The parity of Fe2O3 nano particles was confirmed by EDX. The crystalline size of Iron Oxide nano particles was analyzed using X-ray Diffraction (XRD) spectrum. The functional groups are identified in Fourier Transform Infrared Spectroscopy (FTIR). The surface morphology of the Iron Oxide Nano particles is found from Scanning Electron Microscopy (SEM). The optical properties are determined by using UV-Visible Spectroscopy. Thus, the so-formed nano particles were Fe2O3.


2002 ◽  
Vol 16 (19) ◽  
pp. 2885-2899
Author(s):  
K. YADAIAH ◽  
ABDUL NAYEEM ◽  
M. SOMI REDDY ◽  
M. NAGABHOOSHANAM

The polycrystalline (CdSe)1-x (ZnS)x semiconductor powder with (0 ≤ x ≤ 1) has been prepared by controlled co-precipitation method from an alkaline medium using thiourea as a sulphide ion source. Pellets are made out of these powders under 10 tonnes/sq.cm pressure and are sintered at 800°C for 2 hours in nitrogen atmosphere. X-ray studies have indicated that the compounds are polycrystalline in nature with mixed hexagonal structure of CdSe with x = 0-0.3 and cubic structure of ZnS with x = 1. The chemical homogeneity of the samples was observed from the EDAX and also noted that the atomic contents present were as per the constituents taken in the solution. Lattice parameters (a and c) of all the compounds are determined from the X-ray data and are found to decrease with the increase in ZnS content. It is also observed that the grain size decreases with the increase in x from 0-0.6 and later it remained almost the same till x reaches 0.9. Optical studies indicated that the energy gap was as high as 5.2 eV and remained almost same throughout the composition range x = 0-1. Scanning electron micrographs have shown platelet like structure in CdSe and mixed compounds where as a mixed Cubic and Hexagonal structure in ZnS. The results are explained based on different phases present in the compounds.


2018 ◽  
Vol 24 (8) ◽  
pp. 5691-5694 ◽  
Author(s):  
D Sathisha ◽  
K. Gopalakrishna Naik

Nickel oxide (NiO) nanostructures were synthesized by hydrothermal method using ethylene glycol and double distilled water as solvent in 3:2 volume ratio. The synthesized nanostructures were characterized by XRD, FESEM, EDX, FTIR, and UV-visible spectroscopy. XRD result shows that the synthesized nanostructures are polycrystalline in nature. FESEM images show the growth of NiO nanowires. The elemental compositions of the samples were analyzed by EDS. Fourier transform infrared (FTIR) spectroscopy confirms the existence of Ni–O bond in the sample. Optical band gap energy of about 3.71 eV was calculated from the UV-visible absorption measurement.


2011 ◽  
Vol 2011 ◽  
pp. 1-6
Author(s):  
N. M. Huang

We report the synthesis of nanorods in a nonionic sugar-based water-in-oil (w/o) microemulsion system using food grade sucrose ester as biosurfactant. was formed by mixing indium (III) chloride and thioacetamide in the water core of the microemulsion system. The as-prepared yellowish was characterized by X-ray diffractometry (XRD), UV-visible absorption spectroscopy (UV-Vis), transmission electron microscopy (TEM), and Fourier transform infrared spectroscopy (FTIR). Formation of spherical or rod-like nanomaterials was dependent on reaction time. Rod-like , arranged in bundles, was formed only after 2 days of reaction time. Upon longer aging time, a mixture of rod-like and spherical was formed. A plausible formation mechanism of the nanorods in the sucrose ester microemulsion was postulated. The diameter of the nanorods was found to be very small, which is  nm with aspect ratio of 20 : 1 (length : diameter).


2010 ◽  
Vol 663-665 ◽  
pp. 243-246
Author(s):  
Han Mei Hu ◽  
Chong Hai Deng ◽  
Qiang Fang ◽  
Ya Gao ◽  
Meng Wei Song

In this paper, we report a simple two-step approach (microwave-calcinating) to prepare skin-colored N-doped ZnO nanocrystals. X-ray diffraction (XRD), field emission scanning electron microscopy (FESEM), X-ray photoelectron spectroscopy (XPS) and UV-visible absorption were used to characterize the as-synthesized products. The FESEM results reveal the products mainly take on the morphology of porous flake constructed by 20 nm nanoparticles. UV-Vis spectrum shows a strong absorption peak located at 384nm.


2019 ◽  
Vol 19 (2) ◽  
pp. 422
Author(s):  
Siham Lhimr ◽  
Saidati Bouhlassa ◽  
Saidati Bouhlassa ◽  
Saidati Bouhlassa ◽  
Bouchaib Ammary ◽  
...  

In this paper we study the effects of different molar ratio R of Zn2+ to OH– (R= nOH–/nZn(II) of the precursor was investigated by varying the amount of NaOH. Samples have been synthesized by the colloidal method at room temperature using (ZnCl2), citric acid (C6H8O9·H2O) and sodium hydroxide (NaOH). The formation of ZnO/C composite was characterized by The X-ray diffraction patterns indicated a high crystallinity and nanocrystalline size of ZnO with hexagonal wurtzite structure. The morphologies of the particles have been studied with a scanning electronic microscopy (SEM). The existence of carbon into the composite was detected by FTIR and EDS. The optical band gap of various ZnO/C composite was calculated from UV-Visible absorption measurement varied in the range 3.301 to 3.282 eV according to R values.


2014 ◽  
Vol 10 (3) ◽  
pp. 2430-2440
Author(s):  
N. Belghiti ◽  
M. Bouachrine ◽  
K. Alimi

The goal of this work is to study a new copolymer which combines the Ecbz properties and those Ant. First, we describe the route for preparing the new copolymer. Then, we report characterization measurements based on solid-state Nuclear Magnetic Resonance (CP-MAS 13C NMR), Raman, IR absorption, UV–visible absorption, photoluminescence spectroscopy, Scanning Electron Microscopy (SEM), and X-ray diffraction.


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