No abstract

Multi‐walled carbon nanotubes (CNTs) and nitrogen‐doped carbon (CNx) nanotubes have been synthesized by the aerosol‐assisted chemical vapour deposition (CVD) method. The samples were prepared from toluene and acetonitrile taken in different proportion. The structure of CNTs and CNx nanotubes was compared using first‐ and second‐order Raman spectra. The disorder‐induced D band was found to up‐shift with increase of the acetonitrile fraction. The ID/IG and IG′/IG ratios showed the opposite dependence on the doping level of CNTs. Both kinds of the substitute nitrogen: graphitic‐like and pyridinic‐like contribute to the disorder in CNx nanotube layers. (© 2008 WILEY‐VCH Verlag GmbH & Co. KGaA, Weinheim)

Nitrogen-containing multi-wall carbon nanotubes (N-MWCNTs) were synthesized using aerosol assisted chemical vapor deposition (CVD) techniques in conjunction with benzylamine:ferrocene or acetonitrile: ferrocene mixtures. Different amounts of toluene were added to these mixtures in order to change the N/C ratio of the feedstock. X-ray photoelectron and near-edge X-ray absorption fine structure spectroscopy detected pyridinic, pyrrolic, graphitic, and molecular nitrogen forms in the N-MWCNT samples. Analysis of the spectral data indicated that whilst the nature of the nitrogen-containing precursor has little effect on the concentrations of the different forms of nitrogen in N-MWCNTs, the N/C ratio in the feedstock appeared to be the determining factor. When the N/C ratio was lower than ca. 0.01, all four forms existed in equal concentrations, for N/C ratios above 0.01, graphitic and molecular nitrogen were dominant. Furthermore, higher concentrations of pyridinic nitrogen in the outer shells and N 2 molecules in the core of the as-produced N-MWCNTs suggest that the precursors were decomposed into individual atoms, which interacted with the catalyst surface to form CN and NH species or in fact diffused through the bulk of the catalyst particles. These findings are important for a better understanding of possible growth mechanisms for heteroatom-containing carbon nanotubes (CNTs) and therefore paving the way for controlling the spatial distribution of foreign elements in the CNTs using CVD processes.