Search

The growing interest in nanomaterials in different application fields calls for the implementation of simple, economically appealing, and efficient preparative methods. Among the wide variety of nanomaterials, carbon nanostructures have a special place due to their potential technological applications. Here, we present a fast, cheap, and easy-to-implement microwaveassisted method for the preparation of carbon nanotubes (CNTs) and carbon fibers (CFs) at room pressure conditions. The synthesis involves heating a mixture of graphite and ferrocene contained in a simple glass tube using a conventional microwave oven. A mixture of multi-walled carbon nanotubes (MWCNTs) and [Fe.sub.3][O.sub.4] magnetic nanoparticles were obtained quickly (less than 30 s) and in good yields. The products were characterized using scanning electron microscopy (SEM), transmission electron microscopy (TEM), powder X-ray diffraction (XRD), and Raman spectroscopy. Key words: nanomaterials, multi-walled carbon nanotube (MWCNT), microwave synthesis, carbon nanostructures. L'interet grandissant pour les nanomateriaux dans differents champs d'application constitue un motif pour la mise au point de procedes simples, economiques et efficaces pour les fabriquer. Parmi la grande variete de nanomateriaux, les nanostructures de carbone occupent une place particuliere en raison de leurs possibles applications technologiques. Dans le present article, nous presentons un procede assiste par microondes pour la synthese de nanotubes de carbone (NTC) et de fibres de carbone (FC) a pression atmospherique qui est rapide, economique et facile a mettre en ceuvre. La synthese consiste a chauffer un melange de graphite et de ferrocene dans une simple eprouvette de verre au moyen d'un four a microonde de cuisine. Nous avons obtenu un melange de nanotubes de carbone a parois multiples (NTCPM) et de nanoparticules de [Fe.sub.3][O.sub.4] magnetiques, et ce, rapidement (moins de 30 secondes) et avec de bons rendements. Nous avons caracterise les produits par microscopie electronique a balayage (MEB), microscopie electronique en transmission (MET), diffraction des rayons X (DRX) sur poudre et spectroscopie Raman. [Traduit par la Redaction] Mots-cles: nanomateriaux, NTCPM, synthese par microondes, nanostructures de carbone., Introduction Carbon is a remarkable element that can be considered as the key element of living entities. Thanks to its ability to bond to itself forming oligomers and polymers, it [...]

Advanced oxidation processes stand as green alternatives for the decontamination of waste waters. Photocatalysis is an advanced oxidation process in which a semiconductor material absorbs photon energy and triggers redox reactions capable of degrading organic pollutants. Titanium dioxide (TiO2, titania) represents one of the most popular choices of photocatalytic materials, however the UV-activation of its anatase phase and its high charge recombination rate decrease its photocatalytic activity and weaken its potential. Graphene oxide is a 2D carbon nanomaterial consisting of exfoliated sheets of hexagonally arranged carbons decorated with oxygen- and hydrogen- functional groups. Composite nanomaterials consisting of titania nanoparticles and graphene oxide have proven to enhance the photocatalytic activity of pure TiO2. In this review, we present a thorough literature review of ternary nanocomposites based on synthesized or commercial titania nanoparticles and GO (or reduced GO) particularly used for the photodegradation of dyes. GO/TiO2 has been enriched primarily with metals, semiconductors and magnetic nanomaterials, proving a superior dye degradation performance and reusability compared to bare TiO2. Ongoing challenges and perspectives are outlined. [ABSTRACT FROM AUTHOR]

Functionalized carbon nanospheres have been synthesized in situ via a facile chemical vapor deposition strategy, fabricated by the pyrolysis of toluene/ethanol mixtures at different percentages (0, 1, 2, 3, 4, and 5 wt% of ethanol). The as-grown nanospheres have been characterized using transmission electron microscopy, scanning electron microscopy, Raman and Fourier transform infrared spectroscopy, x-ray diffraction, nitrogen adsorption, zeta potential measurements and x-ray photoelectron spectroscopy. Results indicate that the incorporation of ethanol in the precursor solution reflected in the presence of oxygen and hydrogen functional groups, the highest functionalized nanospheres without compromising the morphology of the sample were yielded at 3 wt% concentration. These in situ added functional groups rendered the carbon nanostructures enhancedly dispersible and stable in water, avoiding post-synthesis and harsh chemicals processing; envisaging thus applications of the nanospheres in the biomedical field where hydrophilicity of the nanomaterials is mandatory. [ABSTRACT FROM AUTHOR]

Due to the need of integrated circuit in the current silicon technology, the formation of graphene on Si wafer is highly desirable, but is still a challenge for the scientific community. In this context, we report the direct growth of graphene on Si(111) wafer under appropriate conditions using an electron beam evaporator. The structural quality of the material is investigated in detail by reflection high energy electron diffraction, Auger electron spectroscopy, X-ray photoemission spectroscopy, Raman spectroscopy, high resolution scanning electron microscopy, atomic force microscopy, and scanning tunneling microscopy. Our experimental results confirm that the quality of graphene is strongly dependent on the growth time during carbon atoms deposition. [ABSTRACT FROM AUTHOR]

Background: Driven by the potential biological applications of graphene, many groups have studied the response of cells exposed to graphene oxide (GO). In particular, investigations of bacteria indicate that there are 2 crucial parameters, which so far have only been investigated separately: GO size and exposure methodology. Our study took into account both parameters. We carefully characterized the samples to catalog sizes and structural properties, and tested different exposure methodologies: exposure in saline solution and in the presence of growth media. Furthermore, we performed experiments with peripheral blood mononuclear cells exposed to our GO materials. Methods: Atomic force microscopy, scanning electron microscopy, Raman spectroscopy, X-ray photoelectron spectroscopy and transmission electron microscopy were used to characterize the morphology and composition of different samples of GO: GO-H2O, GO-PBS and GO-MG. Our samples had 2D sizes of ~100 nm (GO-H2O and GOPBS) and >2 μm (GO-MG). We tested antibacterial activity and cytotoxicity toward peripheral blood mononuclear cells of 3 different GO samples. Results: A size-dependent growth inhibition of Escherichia coli (DH5 α) in suspension was found, which proved that this effect depends strongly on the protocol followed for exposure. Hemocompatibility was confirmed by exposing peripheral blood mononuclear cells to materials for 24 hours; viability and apoptosis tests were also carried out. Conclusions: Our experiments provide vital information for future applications of GO in suspension. If its antibacterial properties are to be potentiated, care should be taken to select 2D sizes in the micrometer range, and exposure should not be carried out in the presence of grow media. [ABSTRACT FROM AUTHOR]

Here the authors report the use of either furnace heating or Joule heating to pacify the exposed graphene edges by loop formation in a novel graphitic nanoribbon material, grown by chemical vapor deposition. The edge energy minimization process involves the formation of loops between adjacent graphene layers within the nanoribbons. A comparison is made of the similarities and differences between the loop structures formed using these two methods. An estimation of the temperature of these graphitic nanoribbons during Joule heating is also reported based on the melting and evaporation of Pt nanoparticles. [ABSTRACT FROM AUTHOR]

Graphene nanoribbons can exhibit either quasi-metallic of semiconducting behavior, depending on the atomic structure of their edges. Thus, it is important to control the morphology and crystallinity of these edges for practical purposes. We demonstrated an efficient edge-reconstruction process, at the atomic scale, for graphitic nanoribbons by Joule heating. During Joule heating and electron beam irradiation, carbon atoms are vaporized, and subsequently sharp edges and step-edge arrays are stabilized, mostly with either zigzag- or armchair-edge configurations. Model calculations show that the dominant annealing mechanisms involve point defect annealing and edge reconstruction. [ABSTRACT FROM AUTHOR]