Using a two-dimensional self-consistent field calculation, we determin
e the equilibrium morphology of thin films of ABC triblock copolymers
confined between hard, smooth plates. The B segment is chosen to be th
e central block and all the blocks are incompatible. The chains microp
hase-segregate into a lamellar phase, with the stripes either perpendi
cular or parallel to the walls. When all the monomer-surface interacti
ons are identical, the perpendicular orientation has the lowest free e
nergy. When a repulsion is introduced between the surface and the A an
d C monomers, the surface interactions further stabilize the perpendic
ular orientation. At strong surface interactions, the morphology of th
e perpendicular structure is controlled by the overall thickness of th
e molten layer. In comparing diblocks to triblocks as candidates for f
orming laterally patterned films, our work indicates that triblocks po
ssess distinct advantages over diblocks. First, no special effort need
s to be taken to establish neutral surfaces. Second, the film does not
have to be confined between two substrates. Thus, triblocks can be us
ed to fabricate patterned polymer surfaces, which can be used for nove
l optical or electronic applications.