We have studied the vibrational properties of thin C-60 overlayers dep
osited on ideally H-terminated Si(111) surfaces, by multiple infrared
reflection and high-resolution electron energy-loss spectroscopies. We
find that the Si-H interface remains intact upon C60 deposition: the
Si-H stretching mode frequency, initially at 2083.8 cm(-1), shifts dow
nward to 2062 cm(-1), and broadens while keeping the same integrated i
ntensity. Due to the symmetry-breaking effect at the surface on the ad
sorbed C60 molecules, a new IR band is observed at 1445 cm(-1) which i
s mainly s-polarised. No evidence for chemical interaction between C60
and H/Si(111)-(1 x 1) is found, pointing to van der Waals-type bondin
g. From the relative intensities of the dipole-active and -inactive mo
des in HREELS in the specular direction, and from the angular width of
the scattered elastic peak, the growth of an ordered film is inferred
.