Pyrocarbon materials containing various amounts of boron have been pre
pared by LPCVD from BCl3-C3H8-H-2 precursor mixtures. By increasing th
e BCl3/(C3H8 + BCl3) ratio up to 85%, the incorporation of boron can r
each 33 at.%. A small amount of boron (e.g. 8 at.%) highly enhances th
e structural anisotropy of pyrocarbon, as evidenced by optical microsc
opy, X-ray diffraction and transmission electron microscopy (selected
area diffraction and lattice fringes techniques). X-ray photoelectron
spectroscopy has shown that a large fraction of the boron atoms are in
cluded by substitution in the carbon layers; the remaining boron atoms
belong to a boron-rich amorphous part of the material. As the boron c
ontent increases beyond 8 at.%, the structural anisotropy of the boron
-rich pyrocarbon decreases, due to the limited growth and stacking of
the carbon layers. Also, amorphous boron-rich regions are more and mor
e abundant as the total amount of boron increases. The oxidation resis
tance of the C(B) materials is better than that of pure pyrocarbon. Th
is is mainly due to the improvement of the structural organization for
the low boron content materials and to the coating of the whole mater
ial with a stable boron oxide for materials with a higher boron conten
t. Copyright (C) 1996 Elsevier Science Ltd