15 research outputs found

    Enhanced magnetic properties of polymer-magnetic nanostructures synthesized by ultrasonication

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    Polymer based nickel (Ni) and cobalt (Co) co-doped ferrites were prepared by adept ultrasonication route. Different concentrations of polymer [polyvinyl alcohol (PVA)] (0.2 g and 0.5 g) was added as a surfactant to the magnetic particles. The phase purity of Ni-Co ferrites (spinel structure) was confirmed by X-ray diffraction (XRD). Enhanced saturation magnetization of polymer based magnetic nanoparticles due to shape anisotropy and size. 0.2 wt% doped ferrite showed superparamagnetic characteristics with blocking temperature above room temperature. Hence, ultrasonication route is a rapid and effective technique for tailoring size and morphology of magnetic nanostructure that could be useful in magnetic-sensor applications

    Enhanced magnetic properties of polymer-magnetic nanostructures synthesized by ultrasonication

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    Polymer based nickel (Ni) and cobalt (Co) co-doped ferrites were prepared by adept ultrasonication route. Different concentrations of polymer [polyvinyl alcohol (PVA)] (0.2 g and 0.5 g) was added as a surfactant to the magnetic particles. The phase purity of Ni-Co ferrites (spinel structure) was confirmed by X-ray diffraction (XRD). Enhanced saturation magnetization of polymer based magnetic nanoparticles due to shape anisotropy and size. 0.2 wt% doped ferrite showed superparamagnetic characteristics with blocking temperature above room temperature. Hence, ultrasonication route is a rapid and effective technique for tailoring size and morphology of magnetic nanostructure that could be useful in magnetic-sensor applications

    Novel multifunctional of magnesium ions (Mg++) incorporated calcium phosphate nanostructures

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    Magnesium ions incorporated calcium phosphate was synthesized by wet chemical route and followed by microwave assisted method. XRD analysis was confirmed that the presence of calcium phosphate (hydroxyapatite). TEM analysis was exhibited rod-like morphology. XRF results were showed the percentage of calcium, phosphate, magnesium and oxygen. There was a slight blue shift observed in magnesium ions based samples. Higher magnesium (0.1 Mg-HAp) was revealed the greater discharging time with capacitance voltage (0.55 V). Magnesium based calcium phosphate was showed prolonged rate of drug release. At higher frequency, the Nyquist plot was showed the electrochemical behavior, however at lower frequency, revealed mass transfer process. Magnesium ions tailor the specific capacitance of calcium phosphate. Therefore, magnesium ions based phosphate samples could be an outstanding multifunctional candidate for drug release and supercapacitor applications

    Enhanced anticorrosion properties of nitrogen ions modified polyvinyl alcohol/Mg-Ag ions co-incorporated calcium phosphate coatings

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    Nitrogen ions (70 keV) were implanted on composite coatings containing polymer/Mg (magnesium)–Ag (silver) ions co-incorporated hydroxyapatite which is developed by microwave irradiation. Average crystallite size of modified coatings is reduced to 80% compared to pristine. The variation of bond strength of modified coatings is realized. The electrical resistance (77%), microhardness (4.3%), roughness (4.5 times) and pore size are enhanced on the modified coatings. Superhydrophilic surface is tuned to hydrophobic on implantation. At higher fluence (1×1017 ions/cm2) depicted an enhanced corrosion potential compared to the other coatings. Thus, the new insight of modified coatings is realized by correlating phase-structure, surface and anticorrosion

    Effect of Ag-Decorated BiVO4 on Photoelectrochemical Water Splitting: An X-ray Absorption Spectroscopic Investigation

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    Bismuth vanadate (BiVO4) has attracted substantial attention on account of its usefulness in producing hydrogen by photoelectrochemical (PEC) water splitting. The exploitation of BiVO4 for this purpose is yet limited by severe charge recombination in the bulk of BiVO4, which is caused by the short diffusion length of the photoexcited charge carriers and inefficient charge separation. Enormous effort has been made to improve the photocurrent density and solar-to-hydrogen conversion efficiency of BiVO4. This study demonstrates that modulating the composition of the electrode and the electronic configuration of BiVO4 by decoration with silver nanoparticles (Ag NPs) is effective in not only enhancing the charge carrier concentration but also suppressing charge recombination in the solar water splitting process. Decoration with a small number of Ag NPs significantly enhances the photocurrent density of BiVO4 to an extent that increases with the concentration of the Ag NPs. At 0.5% Ag NPs, the photocurrent density approaches 4.1 mA cm−2 at 1.23 V versus a reversible hydrogen electrode (RHE) under solar simulated light illumination; this value is much higher than the 2.3 mA cm−2 of pure BiVO4 under the same conditions. X-ray absorption spectroscopy (XAS) is utilized to investigate the electronic structure of pure BiVO4 and its modification by decoration with Ag NPs. Analytical results indicate that increased distortion of the VO4 tetrahedra alters the V 3d–O 2p hybridized states. Additionally, as the Ag concentration increases, the oxygen vacancy defects that act as recombination centers in BiVO4 are reduced. In situ XAS, which is conducted under dark and solar illumination conditions, reveals that the significantly enhanced PEC performance is attributable to the synergy of modulated atomic/electronic structures and the localized surface plasmon resonance effect of the Ag nanoparticles
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