The bonding and thermal reactivity of thin a-SiC:H films have been
studied and compared with that of methyl
groups on single-crystalline Si and in thick polymer films. The
films were deposited on silicon substrates at
200 K by hot-wire chemical vapor deposition (CVD) using methylsilane
(CH3SiH3) as the precursor.
The
resulting films were probed by in situ multiple internal
reflection−Fourier transform infrared (MIR−FTIR)
spectroscopy, and the thermal decomposition products were measured by
temperature-programmed reaction/desorption (TPR/D). According to MIR−FTIR measurements, hydrogen
is present in the films in the form
of mixed silicon hydride species (SiH, SiH2, and
SiH3) and intact methyl groups. TPR/D and
MIR−FTIR
annealing studies following growth at 200 K indicate that the film is
stable up to 550 K. Above 550 K, a
number of thermal etching processes are observed, leading to silane and
methylsilane evolution at 600 K,
followed by the loss of methane and molecular hydrogen by 780 K.
Annealing studies show that the SiH3
species are more reactive at thermal energies than are methyl groups.
The stability of methyl groups and the
silicon mono- and dihydride groups in the films largely parallels that
observed on single-crystalline silicon,
but more reaction pathways are available in the thin films.
Mechanisms for the film growth and thermal
decomposition are proposed.