77 research outputs found
Synthesis of Mesoporous Silica@Co–Al Layered Double Hydroxide Spheres: Layer-by-Layer Method and Their Effects on the Flame Retardancy of Epoxy Resins
Hierarchical mesoporous silica@Co–Al layered double hydroxide (m-SiO2@Co–Al LDH) spheres were prepared through a layer-by-layer assembly process, in order to integrate their excellent physical and chemical functionalities. TEM results depicted that, due to the electrostatic potential difference between m-SiO2 and Co–Al LDH, the synthetic m-SiO2@Co–Al LDH hybrids exhibited that m-SiO2 spheres were packaged by the Co–Al LDH nanosheets. Subsequently, the m-SiO2@Co–Al LDH spheres were incorporated into epoxy resin (EP) to prepare specimens for investigation of their flame-retardant performance. Cone results indicated that m-SiO2@Co–Al LDH incorporated obviously improved fire retardant of EP. A plausible mechanism of fire retardant was hypothesized based on the analyses of thermal conductivity, char residues, and pyrolysis fragments. Labyrinth effect of m-SiO2 and formation of graphitized carbon char catalyzed by Co–Al LDH play pivotal roles in the flame retardance enhancement
Probing the Nature of Defects in Graphene by Raman Spectroscopy
Raman Spectroscopy is able to probe disorder in graphene through
defect-activated peaks. It is of great interest to link these features to the
nature of disorder. Here we present a detailed analysis of the Raman spectra of
graphene containing different type of defects. We found that the intensity
ratio of the D and D' peak is maximum (~ 13) for sp3-defects, it decreases for
vacancy-like defects (~ 7) and reaches a minimum for boundaries in graphite
(~3.5).Comment: 14 pages, 4 figure
Quantifying defects in graphene via Raman spectroscopy at different excitation energies.
We present a Raman study of Ar(+)-bombarded graphene samples with increasing ion doses. This allows us to have a controlled, increasing, amount of defects. We find that the ratio between the D and G peak intensities, for a given defect density, strongly depends on the laser excitation energy. We quantify this effect and present a simple equation for the determination of the point defect density in graphene via Raman spectroscopy for any visible excitation energy. We note that, for all excitations, the D to G intensity ratio reaches a maximum for an interdefect distance ∼3 nm. Thus, a given ratio could correspond to two different defect densities, above or below the maximum. The analysis of the G peak width and its dispersion with excitation energy solves this ambiguity
Raman spectroscopy as a versatile tool for studying the properties of graphene.
Raman spectroscopy is an integral part of graphene research. It is used to determine the number and orientation of layers, the quality and types of edge, and the effects of perturbations, such as electric and magnetic fields, strain, doping, disorder and functional groups. This, in turn, provides insight into all sp(2)-bonded carbon allotropes, because graphene is their fundamental building block. Here we review the state of the art, future directions and open questions in Raman spectroscopy of graphene. We describe essential physical processes whose importance has only recently been recognized, such as the various types of resonance at play, and the role of quantum interference. We update all basic concepts and notations, and propose a terminology that is able to describe any result in literature. We finally highlight the potential of Raman spectroscopy for layered materials other than graphene
Etude d'un procede de realisation de ceramiques a matrice nitrure de silicium renforcees trichites de carbure de silicium
SIGLEAvailable from INIST (FR), Document Supply Service, under shelf-number : AR 15953 / INIST-CNRS - Institut de l'Information Scientifique et TechniqueMinistere de la Recherche et de la Technologie (MRT), 75 - Paris (France)FRFranc
Development of SiC matrix composites
Communication a : ECCM-5 (5th European conference on composite materials), Bordeaux (France), April 7-10, 1992SIGLEAvailable at INIST (FR), Document Supply Service, under shelf-number : 22419, issue : a.1992 n.45 / INIST-CNRS - Institut de l'Information Scientifique et TechniqueFRFranc
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