Synthesis and Characterization of Cadmium Chalcogenide Nanomaterial (CdE; E=Se/Te) from Novel Single Source Molecular Precursor

2018 ◽  
Vol 14 (2) ◽  
pp. 160-168 ◽  
Author(s):  
Arunendera Kumar Tiwari ◽  
Tripti A. Jain ◽  
Sonal Choubey ◽  
Parmendra Kumar Bajpai

Background: Metal chalcogenide nanomaterials represent an important group of efficient materials, in which the subtle variations in shape, size and phase of nano-powders resulted in physical properties (e.g., electronic and optical) differing from their bulk counterparts, which makes them useful materials for various technological devices. Objective: Synthesis and growth of chalcogenide nano powders from novel single source molecular precursors (i.e., Cd(II) bis-(aminopropane) selenide, Cd(II) bis-(aminoethane) telluride) for the production of cadmium chalcogenide (CdE, E= Se/Te) at nano scale. Method: Single source molecular precursor inserted in quinoline, acting as a coordinating solvent at suitable temperature, yielded vacuum dried powders of CdSe and CdTe nanomaterials. Results: The average particle size was estimated as CdSe ≈ 3 nm, and CdTe ≈ 29 nm from powder X-ray diffraction pattern of synthesized nanoparticles. The produced nanomaterials possess optical properties and calculated energy band gap of nanoparticles as CdTe = 5.2 eV and CdSe = 4.0 eV from UV-Visible spectra. Conclusion: The economical, harmless single source molecular method may be a striking technique to fabricate metal chalcogenide nanoparticles.

Author(s):  
Harish Kumar ◽  
Renu Rani

ZnO nanoparticles were synthesized by microemulsion route in W/S ratio of 5 at room temperature. X-ray diffraction (XRD) pattern reveals wurtzite structure of ZnO nanoparticles. Rod shape of ZnO nanoparticles of average particle size 10.0 to 12.0 nm were observed by transmission electron microscopy. FT-IR spectra confirmed the adsorption of surfactant molecules at the surface of ZnO nanoparticles and presence of Zn-O bonding. Thermal studies were carried out by the differential scanning calorimeter (DSC) techniques. In addition, UV-Visible spectra were employed to estimate the band gap energy of ZnO nanoparticles.


Drug Research ◽  
2017 ◽  
Vol 67 (05) ◽  
pp. 266-270 ◽  
Author(s):  
Ebrahim Izadi ◽  
Ali Rasooli ◽  
Abolfazl Akbarzadeh ◽  
Soodabeh Davaran

AbstractThrough the present study, an eco-friendly method was used to synthesize the gold nanoparticles (GNPs) by using the sodium citrate and extract of the soybean seed as reducing the agents at PH 3. X-Ray diffraction (XRD) method was used to evaluate the crystal structure of as-synthesized NPs and it’s revealed that this method leads to well crystallized GNPs. In order to determine the particle size and their distribution, field emission scanning microscopy (FE-SEM) and dynamic light scattering (DLS) were used. The results showed that, the average particle size distribution of synthesized GNPs in solutions containing of the soybean extract and 1% citrate at PH 3 is about 109.6 and 140.9 nm, respectively. Also, we find that the average size of GNPs is 40 and 33 nm from solutions of citrate and soybean extract, respectively. It was concluded that using the extract of soybean seeds as reducing agent can lead to GNPs with small size and narrow size distribution.


2011 ◽  
Vol 299-300 ◽  
pp. 722-726
Author(s):  
Wen Chang Zhuang ◽  
Yu Xiao Wang

Composites have achieved much attention because of their excellent qualities. Core-shell γ-Fe2O3/Au nanoparticles were prepared by chemical reduction. Their optical properties and morphology were characterized by UV-visible spectrum (UV-vis), X-ray diffraction (XRD) and Transmission Electronic Microscopy (TEM). Furthermore, the average particle size and interface structure were also analyzed using small angle X-ray scattering (SAXS).


2021 ◽  
pp. 1873-1878
Author(s):  
Omar Abdulsada Ali ◽  
Sarmed S.M. Al-Awadi

Well dispersed Cu2FeSnSe4 (CFTSe) nanofilms were synthesized by hot-injection method. The structural and morphological measurements were characterized using XRD (X-ray diffraction), Raman spectroscopy, SEM (scanning electron microscopy), and TEM (transmission electron microscopy). Chemical composition and optical properties of as-synthesized CFTSe nanoparticles were characterized using EDS (energy dispersive spectroscopy) and UV-Vis spectrophotometry. The average particle size of the nanoparticles was about 7-10 nm. The UV-Vis absorption spectra showed that the synthesized CFTS nanofilms have a band gap (Eg) of about 1.16 eV. Photo-electrochemical characteristics of CFTSe nanoparticles were studied and indicated their potential application in photovoltaic applications.


2012 ◽  
Vol 2012 ◽  
pp. 1-9 ◽  
Author(s):  
Numan Salah ◽  
Sami S. Habib ◽  
Zishan H. Khan ◽  
Esam Alarfaj ◽  
Shamshad A. Khan

Thin films of () nanoparticles were synthesized using thermal evaporation method. They were characterized by X-ray diffraction (XRD), scanning electron microscope (SEM), and absorption and transmission spectra. XRD results show that these films are of amorphous nature, while SEM images show nanoparticles with average particle size around 30 nm. No significant changes are observed in morphology of the deposited films by changing concentrations of Te and Ge. The optical behaviors of these films have been studied using the absorption and transmission spectra in the spectral region 400–1100 nm. The absorption, extinction coefficients and refractive index were obtained and investigated in more detail. The optical band gap () values were also determined and are found to decrease from 0.83 to 0.69 eV by increasing the concentration of Ge from 0 to 12. The transmission spectra for the thin films of nanoparticles show strong absorption at wavelength less than 500 nm and become highly transparent at wavelength above 800 nm. No significant changes in the transmission spectra are observed by increasing concentration of Ge. These results might be useful for development of optical disks and other semiconducting devices based on these nanochalcogenides.


2021 ◽  
Vol 11 (10) ◽  
pp. 4638
Author(s):  
Jose Luis López-Miranda ◽  
Rodrigo Esparza ◽  
Marlen Alexis González-Reyna ◽  
Beatriz Liliana España-Sánchez ◽  
Angel Ramon Hernandez-Martinez ◽  
...  

This work reports, for the first time, the synthesis of silver nanoparticles using extracts of the species of Sargassum natans and Sargassum fluitans (AgNPs-S). Their antibacterial and catalytic properties are compared with silver nanoparticles obtained by chemical synthesis (AgNPs-C). The characterization of AgNPs-S and AgNPs-C was carried out using ultraviolet–visible spectroscopy (UV–Vis), dynamic light scattering (DLS), zeta potential, a scanning electron microscope (SEM), X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), and thermogravimetric analysis. The synthesis of silver nanoparticles using Sargassum extract was optimized through varying experimental parameters, such as the type of solvent used to prepare the extract, the volume of the extract, and the pH of the system. The most efficient sample (AgNPs-S) was prepared with a water–ethanol-based extract, using a 3:1 volumetric ratio of extract: a precursor salt with the addition of 1 mL of NaOH pH = 14. The AgNPs-C were spherical in shape, with an average particle size of 11.55 nm, while the AgNPs-S were polyhedral shaped, with an average particle size of 26.39 nm. The synthesized AgNPs-S were found to have significantly higher catalytic activity for the degradation of methylene blue and more effective antibacterial activity against Staphylococcus aureus and Pseudomonas aeruginosa than AgNPs-C.


2012 ◽  
Vol 15 (2) ◽  
pp. 27-34
Author(s):  
Nguyet Thi Thuy Dao ◽  
Duong Phuc Nguyen ◽  
Hien Duc Than

This paper presents the synthesis and characterization of Y3Fe5O12, Gd3Fe5O12 and Dy3Fe5O12 nanoparticles by sol-gel method using initial salts solution of Y(NO3)3, Gd(NO3)3, Dy(NO3)3, Fe(NO3). The lattice constant, crystallite size and particle morphology of these ferrite garnet nanoparticles were studied by using X-ray diffraction and transmission electron microscopy (TEM). The results showed that the garnet samples prepared by this method were formed at 800oC, which is lower than the sintering temperature for ceramic bulk samples (1400oC). The particle size is in the range 25- 40 nm as observed via TEM image and the average particle size was found to be 37nm using Debye- Scherrer formula.


2015 ◽  
Vol 797 ◽  
pp. 391-399
Author(s):  
Justyna Zygmuntowicz ◽  
Aleksandra Miazga ◽  
Łukasz Kamiński ◽  
Katarzyna Konopka

The aim of this study was to synthesis and characterization of nickel aluminate spinel (NiAl2O4) prepared of the equilibrium mixture of Al2O3 and NiO. The materials were produced by the solid phase synthesis. In the experiments the following powders were used: α-Al2O3 TM-DAR from Taimei Chemicals (Japan) of an average particle size 133 nm and density 3.96g/cm3 and NiO powder from Sigma-Aldrich of an average particle size 200 nm and density 6.67 g/cm3. The preliminary calcination was carried out at two temperatures: 1000°C and 1200°C. The final sintering of the samples were performed at 1600°C. The characteristics of the powder after calcination and sintered samples were performed using X-ray diffraction studies (XRD), energy dispersive X-ray analysis (EDS) and scanning electron microscopy (SEM). The study of composites confirmed the presence of nickel aluminate (NiAl2O4) in whole volume of the material.


NANO ◽  
2012 ◽  
Vol 07 (04) ◽  
pp. 1250030
Author(s):  
MADJID TORKAMAN ◽  
AZIZAN AZIZ ◽  
MOHAMAD ABU BAKAR ◽  
SULAIMAN AB GHANI

In this work manganese dioxide (Ramsdellite- MnO2 ) was synthesized at room temperature using a facile electrochemical method. X-ray diffraction (XRD) was used to identify the type and the size of the crystal particle, while field emission scanning electron microscopy (FESEM) and energy filtered transmission electron microscopy (EFTEM) were used to show and identify the morphology of the particles and changes of their morphologies with the increase of reaction times. Fourier transform infrared (FTIR) spectroscopy confirmed the Mn–O bond. Results from XRD showed that optimum time for synthesis Ramsdellite- MnO2 was 9 h. The results of EFTEM showed a mixture of nanospheres and nanorods after 9 h reaction time while a homogenous morphology of nanospheres was detected at 12 h reaction time. Results confirmed on the existence of a correlation between the reaction time and the resulting nanostructures. Moreover, the EFTEM result showed that average particle size for 12 h was (25 ± 7 nm). The variation of calculated specific capacitance (F/g) versus the different scan rate has indicated that the efficiency of synthesized Ramsdellite- MnO2 nanostructures in 12 h reaction time was superior to 9 h.


Author(s):  
Fouzia Gul Samreen ◽  
Rabeea Muzaffar ◽  
Muhammad Nawaz ◽  
Shahla Gul ◽  
Muhammad Asim Raza Basra

Previously the nanoparticles were synthesized by chemical methods which were costly and toxic to bio-systems. Plant extracts provides simpler, eco-friendly and cost efficient method for synthesizing nanoparticles. Lemon peel extract (LPE) was used to synthesize silver nanoparticles (AgNPs) which were evaluated for their antimicrobial effects after optimizing the pH of extract and concentration of both extract and synthesized AgNPs. The characterization of synthesized AgNPs was carried out using Ultraviolet-Visible (UV-Vis) Spectrophotometer, Fourier transform infrared spectroscopy (FTIR), and X-ray diffraction (XRD). Well diffusion method was used to determine the antimicrobial activities of synthesized AgNPs. The presence of phenols and proteins was assumed to reduce the Ag+ ion into silver nanoparticles. The characteristic surface plasmon resonance frequency was observed at 405–425 nm for all varying condition of silver nanoparticles synthesis. Furthermore, results revealed that the synthesized AgNPs remains stable upto 75 days. The average particle size was 2–5 nm, calculated with the help of scherrer’s equation by using XRD data. LPE mediated AgNPs (200 µg/mL) showed significant antimicrobial activity, compared to commercially available nanoparticles while LPE (50 mg/ml) showed no effect. LPE mediated AgNPs might get attention of pharmacists in order to design medicines against different diseases including the infections of bacteria.


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