Sol–Gel Synthesis and Magnetic Studies of Titanium Dioxide Doped with 10% M (M=Fe, Mn and Ni)

TiO2 nanocrystals doped with 1%, 5% and 10% Co/TiO2 and 10% M (M=Fe, Mn and Ni) were prepared by the sol–gel technique and characterized using X-ray diffraction and SQUID. The as-prepared samples are found to be paramagnetic at room temperature, with the magnetic susceptibility following the Curie–Weiss law in the investigated range of 2–370 K. However, transformation from paramagnetism to room-temperature ferromagnetism (RTFM) for the 5% Co/TiO2 was observed by hydrogenating the sample at 573 K while the 1% sample remained paramagnetic. As the percentage of Co was increased from 5% to 10% the Curie temperature increased from 390 K to 470 K determined via extrapolation. Transformation from paramagnetism to room-temperature ferromagnetism (RTFM) was also observed by hydrogenation of 10% Fe/TiO2 at 573 K for 6 h. X-ray diffraction of the hydrogenated sample shows only single phase TiO2 structure suggesting that the observed RTFM may be intrinsic but
magnetic studies may suggest the possibility of Fe nanoparticles.
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Microwave Synthesis of Supported Au and Pd Nanoparticle Catalysts for CO Oxidation

We report the microwave synthesis and characterization of Au and Pd nanoparticle catalysts supported on CeO2, CuO, and ZnO nanoparticles for CO oxidation. The results indicate that supported Au/CeO2 catalysts exhibit excellent activity for low-temperature CO oxidation. The Pd/CeO2 catalyst shows a uniform dispersion of Pd nanoparticles with a narrow size distribution within the ceria support. A remarkable enhancement of the catalytic activity is observed and directly correlated with the change in the morphology of the supported catalyst and the efficient dispersion of the active metal on the support achieved by using capping agents during the microwave synthesis. The significance of the current method lies mainly in its simplicity, flexibility, and the control of the different factors that determine the activity of the nanoparticle catalysts.
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Nature of the reversible paramagnetism to ferromagnetism state in cobalt-doped titanium dioxide

We report that Co0.1Ti0.9O2 prepared by the sol-gel technique is a paramagnet following the Curie–Weiss law: x= x0+C/ (T+theta). However, hydrogenation at 673 K in H2/Ar 5% /95% gas converts a part of the paramagnetic sample to room temperature ferromagnet RTFM and reheating the sample at 573 K in air converts it back to a paramagnet completely. This reversible RTFM transition has been observed for additional cycles by alternately heating in air and H2 / Ar. It is argued that this RTFM is intrinsic and it is due to Co2+–Co2+ exchange interaction mediated by oxygen holes which are produced by hydrogenation but eliminated by oxidation.
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Controlled transformation of paramagnetism to room-temperature ferromagnetism in cobalt-doped titanium dioxide

Samples of Co0.1Ti0.9O22 anatase prepared by the sol–gel technique are found to be paramagnetic at room temperature, with the magnetic susceptibility following Curie–Weiss law in the investigated range of 2–370 K. However, transformation from paramagnetism to room-temperature ferromagnetism ~RTFM! is observed by hydrogenation of the sample at 573 K. The increase in the hydrogenation time from 1 to 6 h increases the remanance, and the Curie temperature 470 K is determined by extrapolation. X-ray photoelectron spectroscopy and transmission electron microscopy of the hydrogenated samples failed to detect Co nanoparticles, suggesting that the observed RTFM in the hydrogenated samples may be intrinsic.
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Surface Enhanced Raman Spectroscopy Using Silver Nanoparticles: The Effects of Particle Size and Halide Ions on Aggregation

A surface enhanced Raman spectroscopy (SERS) investigation of the aggregation of silver nanoparticles formed via LVCC with diameters in the range 5–50 nm were studied. It was found that with 647.1 nm excitation maximum enhancement is observed using particles with 11 nm diameters. Upon addition of sodium halides, enhancement is proportional to the polarizability of the anion. Maximum enhancement was observed when the concentration of the anion is approximately equal to the concentration of the adsorbate.
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Formation of Cobalt Nitrate Hydrate, Cobalt Oxide, and Cobalt Nanoparticles Using Laser Vaporization Controlled Condensation

Herein, we report for the first time the synthesis of cobalt nitrate hexahydrate, cobalt oxide, and cobalt particles formed from a high purity cobalt metal by a novel laser vaporization controlled condensation (LVCC) method under controlled pressures of N2 and O2. The metal vapor produced from a cobalt target in the presence of 50% N2 and 50% O2 results in the formation of cobalt nitrate. We also explored the possibilities of forming cobalt oxide and cobalt nanoparticles by altering the ratio of N2 and O2 present. For example, the synthesis of pure cobalt oxide (CoO) nanoparticles is of importance and challenging since a simple chemical route is complex. We believe that this work will be of significant importance since the present method is promising for the synthesis of metal mono oxides.
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Greetings

Welcome to the Blog dedicated to all things nano. As for myself, I am currently a post-doc at VCU researching nanoparticles as hydrogen storage materails and catalysts for CO oxidation.