Preparation of Cadmium Sulfide Nanostructures in Presence of Polyvinyl Alcohol and Polyvinylpyrrolidone as a Capping Agent and Investigation of Their Structural and Optical Properties

2018 ◽  
Vol 13 (10) ◽  
pp. 1454-1459 ◽  
Author(s):  
Yashar Azizian-Kalandaragh

In this research, cadmium sulfide nanostructures have been prepared by an ultrasound-assisted method in presence of polyvinyl alcohol (PVA) and polyvinylpyrrolidone (PVP) as capping agents. The effects of two different capping agents on the structural and optical properties of cadmium sulfide nanostructures have been investigated by X-ray diffraction (XRD), UV-Vis spectroscopy, scanning electron microscopy (SEM) and Fourier transform Infrared (FT-IR) spectroscopy. The XRD patterns show the high purity of samples. The mean crystal's sizes have been estimated by Debye-Sherrer equation and results show the mean crystallite size is decreasing with increase capping agent concentrations. UV-Vis spectroscopy results show a shift in the peaks and broadening with the PVA and PVP increasing. The broadening of the absorbance spectrum with increasing in capping agent concentrations is due to the quantum confinement of nanostructures. The band gap of prepared samples has been estimated by Tauc equation and graph and results show that the band gaps of samples are increasing with increase in the capping agent's concentration. The SEM images show the distribution of the uncapped sample is different from capped samples. FT-IR spectroscopy results show by increasing of capping agent concentration the energy between the functional group is changed and some peaks show a slight shift.

2018 ◽  
Author(s):  
Koen Vercruysse ◽  
Jayla Moore

This report expands our ongoing research efforts into the non-enzymatic synthesis of melanins. We have explored four different methods for the synthesis of L-DOPA based melanins and evaluated the reproducibility of some of their physic-chemical properties. The melanins were synthesized through the addition of NaOH, tyrosinate or Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Two different approaches for the reactions involving Fe<sup>2+</sup> and H<sub>2</sub>O<sub>2</sub> were tested: a) addition of H<sub>2</sub>O<sub>2</sub> spread out over multiple days or b) addition of H<sub>2</sub>O<sub>2</sub> in one fraction at the start of the reaction. The physic-chemical properties of the melanins explored involved: 1) retention on size exclusion chromatography column, 2) FT-IR spectroscopy, 3) UV-Vis spectroscopy and 4) the capacity to reduce a redox dye, dichlorophenolindophenol. Overall the results obtained indicated that 1) the various synthesis methods lead to melanins with reproducible physic-chemical properties, 2) that the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> are distinctly different from the melanins synthesized in the presence of NaOH or tyrosinate and 3) that no distinctly different melanins were generated when comparing the two different synthesis approaches involving Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Only the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> appeared to possess the capacity to reduce dichlorophenolindophenol.


2020 ◽  
Vol 1 (4) ◽  
pp. 22-25
Author(s):  
Azwan Morni

This study reports a green method for the synthesis of gold nanoparticles (AuNPs) using the aqueous extract of Salix aegyptiaca extract. The effects of gold salt concentration, extract concentration and extract quantity were investigated on nanoparticles synthesis. Novel methods of ideally synthesizing AuNPs are thus thought that are formed at ambient temperatures, neutral pH, low costs and environmentally friendly fashion. AuNPs were characterized with different techniques such as UV–vis spectroscopy, FT-IR spectroscopy, X-ray diffraction, and TEM. FT-IR spectroscopy revealed that gold nanoparticles were functionalized with biomolecules that have primary carbonyl group, -OH groups and other stabilizing functional groups. TEM experiments showed that these nanoparticles are formed with various shapes and X-ray diffraction pattern showed high purity and face centered cubic structure of AuNPs. For electrochemical properties of AuNPs, a modified glassy carbon electrode using AuNPs (AuNPs/GCE) was investigated. The results show that electronic transmission rate between the modified electrode and [Fe (CN)6]3-/4- increased.


2013 ◽  
Vol 834-836 ◽  
pp. 108-111
Author(s):  
Qi Guan Wang ◽  
Wei Zhou ◽  
Su Min Wang ◽  
Wen Zhi Zhang ◽  
Jian Ping Li ◽  
...  

We report on the synthesis and electrochemical properties of multi-walled carbon nanotube (MWNT)/polyaniline (PANI) nanocomposites. The MWNT/PANI composite was prepared through electrochemical polymerization and is confirmed by ultraviolet-visible spectroscopy (UV-vis) spectroscopy and Fourier transform infrared (FT-IR) spectroscopy. The MWNT/PANI nanocomposites show a specific capacitance value as high as 463 F/g.


2014 ◽  
Vol 2014 ◽  
pp. 1-8 ◽  
Author(s):  
Murugan Saranya ◽  
Chella Santhosh ◽  
Rajendran Ramachandran ◽  
Andrews Nirmala Grace

CuS nanostructures have been successfully synthesized by hydrothermal route using copper nitrate and sodium thiosulphate as copper and sulfur precursors. Investigations were done to probe the effect of cationic surfactant, namely, Cetyltrimethylammonium bromide (CTAB) on the morphology of the products. A further study has been done to know the effect of reaction time on the morphology of CuS nanostructures. The FE-SEM results showed that the CuS products synthesized in CTAB were hexagonal plates and the samples prepared without CTAB were nanoplate like morphology of sizes about 40–80 nm. Presence of nanoplate-like structure of size about 40–80 nm was observed for the sample without CTAB. The synthesized CuS nanostructures were characterized by X-ray diffraction (XRD), FE-SEM, DRS-UV-Vis spectroscopy, and FT-IR spectroscopy. A possible growth mechanism has been elucidated for the growth of CuS nanostructures.


2013 ◽  
Vol 750-752 ◽  
pp. 1750-1753
Author(s):  
Rui Jia ◽  
Hai Yan Xu ◽  
Qi Feng ◽  
Wen Bao Li ◽  
Bao Hua Zhu

Four new arylamine-acetylene bridged tetrahedral iron and cobalt carbonyl clusters, [Co2(CO)4(μ-CO)2(η2, μ-TMSCCPh)2N 1, [Fe2(CO)6(μ-CO)(η2, μ-TMSCCPh)NH(PhCC TMS)] 2, [(Co2(CO)6(η2, μ-TMSCCPh))33 and [(Fe2(CO)6(μ-CO)(η2, μ-TMSCCPh))2N(Ph CCTMS)] 4, were obtained by reactions of Co2(CO)8and Fe3(CO)12with the bis [4-((trimethylsilyl) ethynyl) phenyamine and tris [4-((trimethylsilyl) ethynyl) phenyamine compounds in suitable solvent, respectively. All clusters are confirmed by C/H elemental analysis, MS,1HNMR and FT-IR spectroscopy. Furthermore, the electrochemical and optical properties of some clusters were also determined by cyclic voltammogram (CV) analysis and UV-Vis spectra.


2016 ◽  
Vol 34 (2) ◽  
pp. 468-478 ◽  
Author(s):  
Riffat Sagheer ◽  
M. Shahid Rafique ◽  
Farhat Saleemi ◽  
Shafaq Arif ◽  
Fabian Naab ◽  
...  

AbstractIon implantation has a potential to modify the surface properties and to produce thin conductive layers in insulating polymers. For this purpose, poly-allyl-diglycol-carbonate (CR-39) was implanted by 400 keV Au+ ions with ion fluences ranging from 5 × 1013 ions/cm2 to 5 × 1015 ions/cm2. The chemical, morphological and optical properties of implanted CR-39 were analyzed using Raman, Fourier transform infrared (FT-IR) spectroscopy, atomic force microscopy (AFM) and UV-Vis spectroscopy. The electrical conductivity of implanted samples was determined through four-point probe technique. Raman spectroscopy revealed the formation of carbonaceous structures in the implanted layer of CR-39. From FT-IR spectroscopy analysis, changes in functional groups of CR-39 after ion implantation were observed. AFM studies revealed that morphology and surface roughness of implanted samples depend on the fluence of Au ions. The optical band gap of implanted samples decreased from 3.15 eV (for pristine) to 1.05 eV (for sample implanted at 5 × 1015 ions/cm2). The electrical conductivity was observed to increase with the ion fluence. It is suggested that due to an increase in ion fluence, the carbonaceous structures formed in the implanted region are responsible for the increase in electrical conductivity.


2018 ◽  
Author(s):  
Koen Vercruysse ◽  
Jayla Moore

This report expands our ongoing research efforts into the non-enzymatic synthesis of melanins. We have explored four different methods for the synthesis of L-DOPA based melanins and evaluated the reproducibility of some of their physic-chemical properties. The melanins were synthesized through the addition of NaOH, tyrosinate or Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Two different approaches for the reactions involving Fe<sup>2+</sup> and H<sub>2</sub>O<sub>2</sub> were tested: a) addition of H<sub>2</sub>O<sub>2</sub> spread out over multiple days or b) addition of H<sub>2</sub>O<sub>2</sub> in one fraction at the start of the reaction. The physic-chemical properties of the melanins explored involved: 1) retention on size exclusion chromatography column, 2) FT-IR spectroscopy, 3) UV-Vis spectroscopy and 4) the capacity to reduce a redox dye, dichlorophenolindophenol. Overall the results obtained indicated that 1) the various synthesis methods lead to melanins with reproducible physic-chemical properties, 2) that the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> are distinctly different from the melanins synthesized in the presence of NaOH or tyrosinate and 3) that no distinctly different melanins were generated when comparing the two different synthesis approaches involving Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub>. Only the melanins synthesized in the presence of Fe<sup>2+</sup>/H<sub>2</sub>O<sub>2</sub> appeared to possess the capacity to reduce dichlorophenolindophenol.


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