M. Endo et al., STACKING NATURE OF GRAPHENE LAYERS IN CARBON NANOTUBES AND NANOFIBRES, Journal of physics and chemistry of solids, 58(11), 1997, pp. 1707-1712
The structure of multilayer carbon nanotubes is studied using digital
image analysis to interpret high resolution TEM lattice images contain
ing 002 and 100 fringes, in comparision with very thin vapour-grown ca
rbon fibres with nanometer-sized diameter (nanofibres). The results sh
ow that the stacking of graphene shells in a multilayer nanotube glide
with respect to one another, which is in contrast to th: stacking fid
elity of three-dimensional graphite. The diffraction patterns derived
from the fast Fourier transform of the lattice images yield angles of
0 degrees-17 degrees for the 100 lattice planes relative to the ideal
100 direction. The median inter-shell spacing d(002) between carbon na
notubes is also characterized, by using the 100 spacing as an internal
standard, and d(002) range from 3.4 to 3.6 Angstrom. The inter-shell
spacing d(002) decreases with increasing carbon nanotube diameter, whi
ch could be due to a size effect. The so-called vapour-grown carbon fi
bres (VGCFs), obtained by pyrolytic decomposition of hydrocarbon, are
grown through spontaneous deposition of carbon layers on primarily for
med nanotubes. In order to clarify the size effect for layer stacking,
very thin VGCFs with diameter similar to 500 Angstrom, named nanofibe
rs as well as submicron diameter VGCFs, are compared with carbon nanot
ubes, and are discussed in relation with the curvature of graphene lay
ers. Some gently pulverized VGCFs with nm as well as mu m size diamete
rs possess an exposed carbon nanotube at the core of the broken portio
n, suggesting a difference in the stacking structure of the graphene l
ayers between the central core nanotube and the outer pyrolytic sectio
ns. (C) 1997 Elsevier Science Ltd.