68 research outputs found

    Structural Characterisation of Printable Noble Metal/Poly(Vinyl-­Alcohol) Nanocomposites for Optical Applications

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    This work was conducted under the aegis of the Engineering and Physical Sciences Research Council (EPSRC) of the United Kingdom (EP/I004173/1). Amin Abdolvand is an EPSRC Career Acceleration Fellow at the University of Dundee.In order to enable exploitation of noble metal/poly(vinyl-alcohol) nanocomposites for device fabrication, solutions of poly(vinyl-alcohol) suitable for piezo-driven inkjet printing techniques are identified and discussed in terms of their material properties. The printable poly(vinyl-alcohol) medium is then exploited as a host material through the formation of silver or gold nanoparticles in order to create nanocomposites that exhibit a surface plasmon resonance behaviour associated with the small metallic inclusions. To mitigate some of the material redistribution effects associated with the drying of printed droplets containing finely divided materials, the metallic nanoparticles are formed after the printing and drying process is completed, by way of an in-situ reduction of an appropriate metal salt by the poly(vinyl-alcohol)-host matrix itself, which takes place at modest temperatures compatible with most substrate materials. An obvious application for such nanocomposites is in optical elements whereby the surface plasmon resonance associated with the metal is the functional aspect of devices such as sensors or active optical elements. High Resolution Transmission Electron Microscopy was used to examine the dimensions, distribution, morphology and crystal structure of the silver and gold nanoparticles in detail allowing discussion of their suitability for these applications and what further optimisation may be necessary to adequately control their formation.Publisher PDFPeer reviewe

    Controlled Growth of WO3Nanostructures with Three Different Morphologies and Their Structural, Optical, and Photodecomposition Studies

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    Tungsten trioxide (WO3) nanostructures were synthesized by hydrothermal method using sodium tungstate (Na2WO4·2H2O) alone as starting material, and sodium tungstate in presence of ferrous ammonium sulfate [(NH4)2Fe(SO4)2·6H2O] or cobalt chloride (CoCl2·6H2O) as structure-directing agents. Orthorhombic WO3having a rectangular slab-like morphology was obtained when Na2WO4·2H2O was used alone. When ferrous ammonium sulfate and cobalt chloride were added to sodium tungstate, hexagonal WO3nanowire clusters and hexagonal WO3nanorods were obtained, respectively. The crystal structure and orientation of the synthesized products were studied by X-ray diffraction (XRD), micro-Raman spectroscopy, and high-resolution transmission electron microscopy (HRTEM), and their chemical composition was analyzed by X-ray photoelectron spectroscopy (XPS). The optical properties of the synthesized products were verified by UV–Vis and photoluminescence studies. A photodegradation study on Procion Red MX 5B was also carried out, showing that the hexagonal WO3nanowire clusters had the highest photodegradation efficiency

    The effect of heat treatment on superhydrophilicity of TiO

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    TiO2 thin films were synthesized by the sol-gel method and spin coating process. The calcination temperature was changed from 100 to 550 °C. XRD patterns show increasing the content of polycrystalline anatase phase with increasing the calcination temperature. The AFM results indicate granular morphology of the films, which particle size changes from 22 to 166 nm by increasing the calcination temperature. The RBS, EDX and Raman spectroscopy of the films show the ratio of Ti:O ~0.5, and diffusion of sodium ions from substrate into the layer, by increasing the calcination temperature. The UV-vis spectroscopy of the films indicates a red shift by increasing the calcination temperature. The contact angle meter experiment shows that superhydrophilicity of the films depends on the formation of anatase crystal structure and diffused sodium content from substrate to the layer. The best hydrophilicity property was observed at 450 °C calcination temperature, where the film is converted to a superhydrophilic surface after 10 min under 2 mW/cm2 UV irradiation. Water droplet on TiO2 thin film on Si(111), Si(100), and quartz substrates is spread to smaller angles rather than glass and polycrystalline Si substrates under UV irradiation

    Synthesis and characterization of iron oxide nanoparticles using electrical discharge in solution

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    Iron oxide nanoparticles were synthesized for the first time using electrical arc discharge between a pair of highly pure titanium electrode without using metallic iron electrodes in iron chloride salt solution. The produced nanoparticles were characterized using various analyses such as X-ray Diffraction (XRD) and X-ray Photoelectron Spectroscopy (XPS). XRD and XPS analyses showed formation of α-Fe2O3 phase. Microscopic studies on the obtained samples revealed formation of rice like iron oxide nanostructures at 10 minutes of electrical discharge which changed to semi-spherical shape after calcination at 600 oC for 2 hours. The results of Dynamic Light Scattering (DLS) analysis demonstrated formation of 24 nm particles with almost narrow distribution of 11nm, which are increased in size and distribution width by heat treatment. The obtained results verify the potential ability of this technique to achieve monodispersed iron oxide nanoparticles with narrow distribution in a very short tim

    The role of silane gas flow rate on PECVD-assisted fabrication of silicon nanowires

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    Silicon (Si) core–shell nanowires (NWs) were successfully prepared by very high frequency plasma-enhanced chemical vapor deposition technique, and the effect of silane (SiH4) gas flow rates on physicochemical properties of silicon NWs was investigated. Field emission scanning electron microscopy (FESEM), energy-dispersive X-ray spectroscopy, transmission electron microscopy (TEM), X-ray diffraction (XRD) and Raman spectroscopy were used to characterize SiNWs. Structural properties and morphology of NWs were studied as a function of SiH4 gas flow rate. Microscopic analysis revealed the formation of SiNWs with average tip and stem diameters ranging from 18 to 30 and 21 to 67 nm, respectively. Furthermore, the average length of Si NWs calculated based on the FESEM images was about 300–1800 nm. We have found that the growth of SiNWs increased with increasing in SiH4 gas flow rate. XRD, Raman spectra in addition to high-resolution TEM, verified the formation of crystalline SiNWs. A possible growth mechanism was suggested based on our observations

    Synthesis of highly crystalline needle-like silicon nanowires for enhanced field emission applications

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    Needle-like silicon nanowires (SiNWs) were successfully synthesized on gold-coated silicon substrates using a very high frequency plasma enhanced chemical vapor deposition method (VHF-PECVD). The prepared samples were characterized by field emission scanning electron microscopy (FESEM) with energy dispersive X-ray spectroscopy (EDX), high resolution transmission electron microscopy (HRTEM), X-ray diffraction (XRD) and photoluminescence (PL). XRD analysis confirmed formation of single crystalline SiNWs along (111) crystalline planes and microscopic studies revealed formation of NWs with diameters ranging from 10 to 100 nm and lengths of a few micrometers. Furthermore, the presence of gold nanoparticles on the tip of the NWs verified the vapor–liquid–solid growth mechanism of SiNWs. It was also demonstrated that SiNWs are composed of well-crystallized silicon cores and an amorphous shell. The obtained results verified potential application of such structures in field emission displays

    Size measurement of gold and silver nanostructures based on their extinction spectrum: limitations and extensions

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     This paper reports on physical principles and the relations between extinction cross section and geometrical properties of silver and gold nanostructures. We introduce some simple relations for determining geometrical properties of silver and gold nanospheres based on the situation of their plasmonic peak. We also applied, investigated and compared the accuracy of these relations using other published works in order to make clear the effects of shape, size distribution and refractive index of particles’ embedding medium. Finally, we extended the equations to non-spherical particles and investigated their accuracy. We found that modified forms of the equations may lead to more exact results for non-spherical metal particles, but for better results, modified equations should depend on shape and size distribution of particles. It seems that these equations are not applicable to particles with corners sharper than cubes' corners i.e. nanostructures with spatial angles less than π/2 sr

    Stability, size and optical properties of colloidal silver nanoparticles prepared by electrical arc discharge in water

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    We have fabricated and characterised colloidal silver nanoparticles by the electrical arc discharge method in DI water. Size and optical properties of the silver nanoparticles were studied versus different arc currents. Optical absorption indicates a plasmonic peak at 392 nm for 10 A which increases to 398 nm for 20 A arc current. This reveals that by raising the arc current the size of the nanoparticles increases. Optical absorption of silver nanoparticles after 3 weeks shows precipitation of them in a water medium. The effect of different surfactant and stabilizer concentrations such as cethyl trimethylammonium bromide (CTAB), polyvinyl pyrrolidone (PVP), sodium citrate, sodium dodecyl sulfate (SDS), sodium di-2-ethylsulfosuccinate (AOT) and carboxymethyl cellulose (CMC) on the stability of silver nanoparticles was investigated. The colloidal silver nanoparticles with 100 μM concentration were stable for more than 3 months at 50 μM CTAB and 6 months at 10 μM sodium citrate concentration, respectively. SEM images of the sample prepared at 50 μM CTAB concentration reveal uniform and fine nanoparticles. The mean size from TEM images is about 14 nm. TEM images of the sample prepared at 10 μM sodium citrate concentration show a shell of citrate that covers the silver nanoparticles
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