Enhanced optical, morphological, dielectric, and conductivity properties of gold nanoparticles doped PVA/CMC blend as an application in organoelectronic devices

Author(s):  
M. R. Atta ◽  
Qana M. Alsulami ◽  
G. M. Asnag ◽  
A . rajeh

Abstract Stevia rebaudiana plant leaves were used for biosynthesis of gold nanoparticles (AuNPs). Transmission electron microscope ( TEM ) images showed various shapes and sizes of AuNPs. Various amounts of AuNPs were added to polyvinyl alcohol/carboxymethylcellulose ( PVA / CMC , 40/60) via the casting method. The X-ray diffraction (XRD) spectrum of pure blend shows the amorphous nature of the blend. FT-IR spectra showed the interaction between PVA / CMC and AuNPs. The ultra-violet and visible (UV/VIS.) spectra showed emerge new peak of surface plasmon resonance ( SPR ) of AuNPs for the filled samples. SEM images showed bright spots on the sample's surface, which was attributed to AuNPs. AC conductivity exhibited enhancement after the addition of gold nanoparticles. The ε′ and ε″ were reduced with increasing the frequency due to direction dipoles of applied electric field. Because of the mobile charges inside the polymeric backbone, higher values of ε′ and ε″ were observed at low frequencies. The tanδ showed increased with an increase in AuNPs concentration and at the decrease the frequency, as expected.

2013 ◽  
Vol 678 ◽  
pp. 248-252
Author(s):  
K. Kavi Rasu ◽  
Dhandapani Vishnushankar ◽  
V. Veeravazhuthi

Bismuth sulfide (Bi2S3) and Polyvinyl pyrrolidone (PVP) encapsulated Bi2S3 Nanoparticles are synthesized from aqueous solutions at room temperature. Synthesized samples are subjected to UV-Visible Spectroscopy, X-Ray Diffraction (XRD), Scanning electron microscopy (SEM), Energy Dispersive Analysis of X-ray (EDAX), Transmission Electron Microscopy (TEM) and FT-IR studies and their results are compared. X-ray diffraction spectrum reveals the crystalline nature of the synthesized samples. Grain size value of PVP/ Bi2S3 nanoparticles show a decrease when compared to Bi2S3 nanoparticles and this ensures the good encapsulant effect of PVP on Bi2S3 nanoparticles. SEM images show that all the particles in the synthesized sample are nearly equal in size. From the TEM image we conclude that the particle size lies between 30nm to 70nm. Finally the samples are subjected to EDAX studies for determining their composition.


2002 ◽  
Vol 01 (05n06) ◽  
pp. 477-481 ◽  
Author(s):  
LEE DON KEUN ◽  
YOUNG SOO KANG

Silver nanoclusters have been formed by thermal decomposition of Ag-oleate complex. Transmission electron microscopic (TEM) images of the particles showed two-dimensional assembly of particles with diameter of 10.5 nm. Energy-dispersive X-ray (EDX) spectrum and X-ray diffraction (XRD) peaks of the nanoclusters showed the highly crystalline nature of the silver structures. The decomposition of silver-oleate complex was analyzed by Thermo Gravimetric Analyzer (TGA) and the crystallization process was observed by XRD. The removal of the surfactant surrounding silver nanoclusters was measured by FT-IR and SEM images.


2010 ◽  
Vol 09 (05) ◽  
pp. 511-516 ◽  
Author(s):  
P. RAJASULOCHANA ◽  
R. DHAMOTHARAN ◽  
P. MURUGAKOOTHAN ◽  
S. MURUGESAN ◽  
P. KRISHNAMOORTHY

As a part of our ongoing investigation into the use of algae for gold nanoparticle synthesis, we screened the marine alga Kappaphycus alvarezii, to investigate its efficiency to reduce gold ions as well as the formation of gold nanoparticles. In the present work, we report the reaction condition of the alga K. alvarezii with aqueous gold ions for gold nanoparticle synthesis within the biomass extracellularly. The formation of gold nanoparticles was characterized by UV–Vis spectroscopy, Fourier transform infrared (FT-IR) spectroscopy, scanning electron microscopy (SEM), transmission electron microscopy (TEM), and X-ray diffraction (XRD) method. Moreover, we have found that the reaction of gold ions with the K. alvarezii biomass under stationary conditions results in the rapid extracellular formation of gold nanoparticles of spherical morphology. The gold nanoparticles are not toxic to the cells that continued to grow after the biosynthesis of the gold nanoparticles.


2015 ◽  
Vol 2015 ◽  
pp. 1-5 ◽  
Author(s):  
Yuping Tong ◽  
Juntao Ma ◽  
Shunbo Zhao ◽  
Hongyuan Huo ◽  
Hailong Zhang

Well-dispersed nanocrystalline MnCr2O4was prepared by a salt-assisted combustion process using low-toxic glycine as fuel and Mn(NO3)2and Cr(NO3)3·9H2O as raw materials. The obtained products were characterized by X-ray Diffraction (XRD), Fourier Transform Infrared (FT-IR) spectroscopy, Raman spectroscopy, Transmission Electron Microscopy (TEM), and Scanning Electron Microscopy (SEM). The fabrication process was monitored by thermogravimetric and differential thermal analysis (TG-DTA). The phase formation process was detected by XRD, and MnCr2O4single phase with high crystallinity was formed at 700°C. TEM and SEM images revealed that the products were composed of well-dispersed octahedral nanocrystals with an average size of 80 nm. Inert salt-LiCl played an important role in breaking the network structure of agglomerated nanocrystallites.


2008 ◽  
Vol 8 (12) ◽  
pp. 6283-6289
Author(s):  
Yang Dong ◽  
Ying Ma ◽  
Tianyou Zhai ◽  
Yi Zeng ◽  
Hongbing Fu ◽  
...  

Hybrid microgel particles were prepared by one step incubation of poly(N-isopropylacrylamide)-co-poly(acrylic acid) (PNIPAM-co-PAA) and gold nanoparticles (AuNPs). PNIPAM-co-PAA microgel particles were synthesized by surfactant-free emulsion polymerization with different crosslinking densities (4.5 wt.-%, 10 wt.-%, 15 wt.-%, MBA to NIPAM) and AuNPs obtained by trisodium citrate reduction method independently. The effect of crosslinking density of synthesized microgel particles on the loadings of AuNPs was investigated. The results showed that 18±2 nm AuNPs could be well entrapped in the loosely crosslinked (4.5 wt.-%, MBA to NIPAM) PNIPAM-co-PAA microgel particles with high loadings. The final hybrid microgel particles were well characterized by transmission electron microscopy (TEM), UV-vis spectra, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and FT-IR. In particular, the PNIPAM-co-PAA/AuNPs hybrid microgel particles were thermoresponsive and completely reversible with several heating/cooling cycles. Therefore, the PNIPAM-co-PAA/AuNPs hybrid microgel particles allow for combined surface plasmon and thermal switching applications.


Coatings ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 165
Author(s):  
Sandip Madhukar Deshmukh ◽  
Mohaseen S. Tamboli ◽  
Hamid Shaikh ◽  
Santosh B. Babar ◽  
Dipak P. Hiwarale ◽  
...  

In the present work, we have reported a facile and large-scale synthesis of TiO2 nanoparticles (NPs) through urea-assisted thermal decomposition of titanium oxysulphate. We have successfully synthesized TiO2 NPs by using this effective route with different weight ratios of titanium oxysulphate: urea. The structures and properties of TiO2 NPs were confirmed by scanning electron microscope) (SEM), transmission electron microscopy (TEM), thermogravimetric analysis (TGA), fourier transform infrared spectroscopy (FT-IR), ultra violet–visible spectroscopy (UV-vis), and photoluminescence (Pl) techniques. XRD demonstrated that TiO2 NPs holds of anatase crystal phase with crystallizing size 14–19 nm even after heating at 600 °C. TGA, SEM, and TEM images reveal urea’s role, which controls the size, morphology, and aggregation of TiO2 NPs during the thermal decomposition. These TiO2 NPs were employed for photodegradation of Methyl Orange (MO) in the presence of ultraviolet (UV) radiation. An interesting find was that the TiO2 NPs exhibited better photocatalytic activity and excellent recycling stability over several photodegradation cycles. Furthermore, the present method has a great perspective to be used as an efficient method for large-scale synthesis of TiO2 NPs.


Crystals ◽  
2021 ◽  
Vol 11 (5) ◽  
pp. 456
Author(s):  
Fahad A. Alharthi ◽  
Hamdah S. Alanazi ◽  
Amjad Abdullah Alsyahi ◽  
Naushad Ahmad

This study demonstrated the hydrothermal synthesis of bimetallic nickel-cobalt tungstate nanostructures, Ni-CoWO4 (NCW-NPs), and their phase structure, morphology, porosity, and optical properties were examined using X-ray Diffraction (XRD), Fourier-transform infrared spectroscopy (FT-IR), Scanning electron microscopy- energy dispersive X-ray spectroscopy (SEM-EDS), high resolution Transmission electron microscopy (HR-TEM), Brunauer-Emmett-Teller (BET) and Raman instruments. It was found that as-calcined NCW-NPs have a monoclinic phase with crystal size ~50–60 nm and is mesoporous. It possessed smooth, spherical, and cubic shape microstructures with defined fringe distance (~0.342 nm). The photocatalytic degradation of methylene blue (MB) and rose bengal (RB) dye in the presence of NCW-NPs was evaluated, and about 49.85% of MB in 150 min and 92.28% of RB in 90 min degraded under visible light. In addition, based on the scavenger’s study, the mechanism for photocatalytic reactions is proposed.


Catalysts ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 118
Author(s):  
Qui Quach ◽  
Erik Biehler ◽  
Ahmed Elzamzami ◽  
Clay Huff ◽  
Julia M. Long ◽  
...  

The current climate crisis warrants investigation into alternative fuel sources. The hydrolysis reaction of an aqueous hydride precursor, and the subsequent production of hydrogen gas, prove to be a viable option. A network of beta-cyclodextrin capped gold nanoparticles (BCD-AuNP) was synthesized and subsequently characterized by Powder X-Ray Diffraction (P-XRD), Fourier Transform Infrared (FTIR), Transmission Electron Microscopy (TEM), and Ultraviolet-Visible Spectroscopy (UV-VIS) to confirm the presence of gold nanoparticles as well as their size of approximately 8 nm. The catalytic activity of the nanoparticles was tested in the hydrolysis reaction of sodium borohydride. The gold catalyst performed best at 303 K producing 1.377 mL min−1 mLcat−1 of hydrogen. The activation energy of the catalyst was calculated to be 54.7 kJ/mol. The catalyst resisted degradation in reusability trials, continuing to produce hydrogen gas in up to five trials.


Nanomaterials ◽  
2021 ◽  
Vol 11 (1) ◽  
pp. 132
Author(s):  
Jumoke A. Aboyewa ◽  
Nicole R. S. Sibuyi ◽  
Mervin Meyer ◽  
Oluwafemi O. Oguntibeju

Cyclopia intermedia (C. intermedia) is an indigenous South African shrub used to prepare the popular medicinal honeybush (HB) tea. This plant contains high levels of mangiferin (MGF), a xanthonoid that was reported to have numerous biological activities, including anti-tumor activity. MGF and extracts that contain high concentrations of MGF, such as extracts from Mangifera indica L. or mango have been used to synthesize gold nanoparticles (AuNPs) using green nanotechnology. It has previously been shown that when AuNPs synthesized from M. indica L. extracts are used in combination with doxorubicin (DOX) and Ayurvedic medicine, the anti-tumor effects appear to be augmented. It has also been demonstrated that MGF used in combination with DOX resulted in enhanced anti-tumor effects. In this study, C. intermedia (HB) and MGF were used to synthesize HB-AuNPs and MGF-AuNPs, respectively. The physicochemical properties of the AuNPs were characterized by the UV-Visible Spectroscopy (UV-Vis), dynamic light scattering (DLS), Fourier transform infra-red spectroscopy (FTIR), X-ray diffraction spectroscopy (XRD) and high-resolution transmission electron microscopy (HR-TEM). The cytotoxicity of HB-AuNPs and MGF-AuNPs were assessed on human colon (Caco-2), prostate (PC-3) and glioblastoma (U87) cancer cells; as well as normal breast epithelial (MCF-12A) cells using the MTT assay. Both HB-AuNPs and MGF-AuNPs demonstrated relatively low cytotoxicity in these cells. However, when these nanoparticles were used in combination with DOX, the cytotoxicity of DOX was significantly augmented.


2012 ◽  
Vol 600 ◽  
pp. 174-177 ◽  
Author(s):  
Jian Fei Xia ◽  
Zong Hua Wang ◽  
Yan Zhi Xia ◽  
Fei Fei Zhang ◽  
Fu Qiang Zhu ◽  
...  

Zirconia-graphene composite (ZrO2-G) has been successfully synthesized via decomposition of ZrOCl2•6H2O in a water-isopropanol system with dispersed graphene oxide (GO) utilizing Na2S as a precursor could enable the occurrence of the deposition of Zr4+ and the deoxygenation of GO at the same time. Transmission electron microscopy (TEM), Fourier transform infrared spectroscopy (FT-IR) and X-ray diffraction (XRD) techniques were used to characterize the samples. It was found that graphene were fully coated with ZrO2, and the ZrO2 existing in tetragonal phase, which resulted in the formation of two-dimensional composite.


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