We have studied the surface-induced spinodal decomposition in thin fil
ms of deuterated and protonated polystyrene, using He-3 nuclear-reacti
on analysis and dynamic secondary-ion mass spectroscopy. We found that
the amplitude of this process may be modified by a polyisoprene-polys
tyrene diblock copolymer, which segregates predominantly to the surfac
e when admired to the isotopic polystyrene blend. This is due to the r
educed surface attraction of deuterated polystyrene for the increased
surface coverage by diblocks. Finally, the surface directed mode of th
e spinodal decomposition is observed to be extinct for the surface com
pletely covered by copolymers.