Temperature-dependent
interaction of acetonitrile with methanol
and ethanol, as codeposited and sequentially deposited films, was
studied in the 10–130 K window, in ultra high vacuum. Films
in the range of 50–100 monolayers were investigated using temperature-dependent
reflection–absorption infrared spectroscopy (RAIRS), Cs+ ion scattering mass spectrometry, and temperature-programmed
desorption (TPD). Acetonitrile interacts with methanol and ethanol
through intermolecular hydrogen bonding. When a codeposited system
was annealed, acetonitrile underwent a phase segregation at 110 K,
and large changes in the infrared spectrum were observed. The OH stretching
of methanol gave two peaks characteristic of the change to the α-phase
of methanol, while ethanol gave three peaks at the same temperature.
The surface composition of the systems probed by 40 eV Cs+ scattering showed that both the alcohols and the acetonitrile were
of equal intensity below 110 K, while above 110 K the intensity of
the latter went down substantially. We find that the presence of acetonitrile
does not allow ethanol to undergo complete phase transition prior
to desorption, while methanol could do so. This behavior is explained
on the basis of the size, extent of hydrogen bonding, and phase transition
temperature, of the two alcohols. Additional peaks in the hydroxyl
region observed in alcohols in the 110–130 K window may be
used as a signature of the presence of acetonitrile mixed with alcohol,
especially ethanol, and hence this may be used in observational studies
of such molecular environments.