The dynamics of electronic excited states is studied for thin C-60 fil
ms on quartz by second harmonic generation. Time resolved measurements
show that for films thicker than 100 nm a single excited state is obs
erved, which is occupied in faster than 45 ps and decays over 20 ns or
longer. Spectroscopic studies reveal that the state can be excited ov
er the entire visible range following the C-60 absorbance down to 1.6
eV. This indicates that excitonic states below the band gap, most like
ly the lowest singlet and triplet states, determine the suppression me
chanism. For thin films below 100 nm thickness a second excited state
with a substantially reduced lifetime of 70 ps is observed. This state
is attributed to the C-60/substrate interface and gives access to the
coupling between C-60 excitonic states and the immediate environment
of the molecule.