Abstract
X-Ray Absorption Spectroscopy (XAS) on the carbon K edge of carbon nanostructures (nanotubes, nanofibers, nanowalls) is reported here. They are grown on plain SiO2 (8 nm thick)/Si(100) substrates by a Plasma and Hot Filaments-enhanced Catalytic Chemical Vapor Deposition (PE HF CCVD) process. The morphology and the nature of these carbon nanostructures are characterized by SEM, TEM and Raman spectroscopy. According to conditions of catalyst preparation and DC HF CCVD process, carbon nanotubes (CNTs), carbon nanofibers (CNFs), carbon nanowalls (CNWs), carbon nanoparticles (CNPs) with different orientation of the graphene plans or shells can be prepared. From the angular dependence of the incident light and geometrical morphology of the nanostructures, wide variations of the C K-edge intensity of the transitions to the empty π* and σ* states occur. A full lineshape analysis of the XAS spectra has been carried out using a home-made software, allowing estimating the relative proportion of π* and σ* transitions. A geometrical model of the angular dependence with the incidence angle of the light and the morphology of the carbon nanostructures is derived. With normalization to the HOPG (Highly Oriented Pyrolytic Graphite graphite) reference case, a degree of alignment can be extracted which is representative of the localized orientation of the graphitic carbon π bonds, accounting not only for the overall orientation, but also for local defects like impurities incorporation, structural defects ... This degree of alignment shows good agreement with SEM observations. Thus CNTs films display degrees of alignment around 50%, depending on the occurrence of defects in the course of the growth, whereas no special alignment can be detected with CNFs and CNPs, and a weak one (about 20%) is detected on CNWs.
Highlights
Carbon nanotubes (CNTs) have attracted an enormous interest since their first report by Iijima in 1991 [1] for their outstanding properties
Previous papers have been reported on the angular dependence at the C K edge from Multi Wall carbon nanotubes (CNTs) (MWCNT) films grown by classical thermal CCVD (T CCVD) [33] [34], or by plasma-enhanced CCVD [35], and Single Wall CNT (SWCNT) “bucky paper” [36]
We report on a study of the angular dependence at the X-Ray Absorption Spectroscopy (XAS) C K edge concerning films of multiwall carbon nanotubes (MWCNTs), carbon nanofibers (CNFs), carbon nanoparticles (CNPs) and carbon nanowalls (CNWs)
Summary
Carbon nanotubes (CNTs) have attracted an enormous interest since their first report by Iijima in 1991 [1] for their outstanding properties. X-ray absorption spectroscopy (XAS) recorded on the carbon K-edge is a powerful tool to provide chemicallyselective information on the local environment around carbon in solid materials, like CVD diamond [9]-[14], amorphous carbon nitride [15]-[19], amorphous graphitic carbon [20] [21] and CNTs [22]-[26], but the technique is suitable to probe the adsorption of functional organic molecules with information both on the distance and the orientation of the bond [27] [28] This property is due to the angular dependence of the absorption transition. We report on a study of the angular dependence at the XAS C K edge concerning films of multiwall carbon nanotubes (MWCNTs), carbon nanofibers (CNFs), carbon nanoparticles (CNPs) and carbon nanowalls (CNWs) They are grown by a plasma-enhanced CCVD process. It is reported that the carbon nanostructures are highly sensitive to a previous in situ thermal treatment, as an intense adsorption on the outer wall of the nanotubes may strongly affect the absorption
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