58 research outputs found

    Decoration of Carbon Nanotubes with CoO and Co Nanoparticles

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    Multiwall carbon nanotubes (MWNTs) decorated with CoO nanocrystals were synthesized by in-situ thermal decomposition of Co(acac)2 in oleyl amine under reflux conditions open in the air. The CoO/MWNTs composite material can be easily converted to metallic Co/MWNTs through annealing under reducing atmosphere (4%  H2) at 500°C without any significant sintering effect. The composite materials characterized by X-ray diffraction, transmission electron microscopy, and Nuclear Magnetic Resonance (NMR) spectroscopy. The structural and morphological characterization shows that the CoO has cubic face (fcc) and the particles deposited uniformly on the external surface of the carbon nanotubes. In the annealed materials, the NMR shows that the fcc and hcp metallic Co phases coexist with a significant percentage of stacking faults. The magnetic measurements indicated that the CoO/MWNTs composite is largely composed of CoO nanoparticles with uncompensated surface spins. The fluctuations of spins persist in partially reduced CoO grains as shown by nuclear spin-lattice relaxation measurements

    Promotion of the Catalytic Activity of a Ag/Al 2

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    Selective Rhenium Recovery from Spent Reforming Catalysts

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    Hybrid Plasmonic-Superparamagnetic Nanoparticle Clusters: Facile Synthesis and Characterization

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    Decorating Carbon Nanotubes with Metal or Semiconductor Nanoparticles

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    Due to their large chemically active surface and stability at high temperatures carbon nanotubes (CNTs) have been used as a support material for the dispersion and stabilization of metal and semiconductor nanoparticles (NPs). These hybrid materials have found several applications in catalysis, nanoelectronics, optics, nanobiotechnology, etc. Several ways have been described in the literature to immobilize NPs on CNTs and they can be divided into two main pathways: (a) the formation (and stabilization) of metal NPs directly on the carbon nanotube surface, and (b) the connection of chemically modified NPs to carbon nanotubes or to modified CNTs. A plethora of methods for the synthesis of different NPs have been very recently developed. This know-how is now available for the generation of a large variety of new hybrid products in combination with CNTs. A selection of representative examples of the synthesis, properties and applications of NP\u2013CNTs is here reported and discussed

    Catalytic reduction of N 2 O with CH 4 and C 3 H 6 over Ag-Rh/Al 2 O 3 bimetallic catalyst in the presence of oxygen

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    Abstract: A study of nitrous oxide (N 2 O) reduction with methane (CH 4 ) and propene (C 3 H 6 ) in the presence of oxygen (5%) over Ag/Al 2 O 3 , Rh/Al 2 O 3 and Ag-Rh/Al 2 O 3 catalysts, with Ag and Rh loadings of 5 wt% and 0.05 wt% respectively, has been performed. From the results, it was observed that the Ag-Rh bimetallic catalyst was the most active for both nitrous oxide removal (more than 95%) and hydrocarbon oxidation. This high activity seems to be connected with a synergistic effect between Ag and Rh. The findings from X-ray diffraction and X-ray photoelectron spectroscopy studies showed also, that there were no strong interactions (eg alloying) between Ag and Rh

    Blue Phase Range Widening Induced by Laponite Nanoplatelets in the Chiral Liquid Crystal CE8

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    We report on the widening of blue phase range induced by surface-functionalised laponite nanoplatelets dispersed in a chiral liquid crystal. The results are obtained by means of high-resolution ac calorimetry and optical microscopy and they are reproducible upon heating and cooling, identifying thermodynamically stable blue phases. It is shown that nanoplatelets target mostly the cubic structure of blue phase I and increase its temperature stability range by a factor of two. The present results are in agreement with recent findings that anisotropic nanoparticles tend to effectively stabilise blue phase I. © 2015 Copyright © Taylor & Francis Group, LLC

    CdSe nanoparticles dispersed in ferroelectric smectic liquid crystals: Effects upon the smectic order and the smectic-A to chiral smectic-C phase transition

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    Spherical CdSe nanoparticles, surface-treated with oleylamine and tri-octylphosphine, dispersed in ferroelectric liquid crystals, can efficiently target disclination lines, substantially altering the macroscopic properties of the host compound. Here we present an ac calorimetry and x-ray diffraction study demonstrating that for a large range of nanoparticle concentrations the smectic-A layer thickness increases monotonically. This provides evidence for enhanced accumulation of nanoparticles at the smectic layers. Our results for the Smectic-A (SmA) to chiral smectic-C (SmC*) phase transition of the liquid crystal S-(+)4-(2′-methylbutyl)phenyl-4 ′-n-octylbiphenyl-4-carboxylate (CE8) reveal that the character of the transition is profoundly changed as a function of the nanoparticle concentration. Large transition temperature shifts are recorded. Moreover, the heat-capacity peaks exhibit a crossover trend to a step-like anomaly. This behavior may be linked to the weakening of the SmA and SmC* order parameter coupling responsible for the observed near-tricritical, mean-field character of the transition in bulk CE8. At lower temperatures, the presence of nanoparticles disrupts the phase sequence involving the tilted hexatic phases most likely by obstructing the establishment of long-range bond-orientational order. © 2013 American Physical Society

    Nanoparticle-induced twist-grain boundary phase

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    By means of high-resolution ac calorimetry and polarizing optical microscopy, it is demonstrated that surface-functionalized spherical CdSSe nanoparticles induce a twist-grain boundary phase when dispersed in a chiral liquid crystal. These nanoparticles can effectively stabilize the one-dimensional lattice of screw dislocations, thus establishing the twist-grain boundary order between the cholesteric and the smectic-A phases. A Landau-de Gennes-Ginzburg model is used to analyze the impact of nanoparticles on widening the temperature range of molecular organizations possessing a lattice of screw dislocations. We show that in addition to the defect-core-replacement mechanism, the saddle-splay elasticity may also play a significant role. © 2014 American Physical Society
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