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We report observations of chain stretching in diblock copolymer monolayers on the surface of a selective solvent. Using neutron reflectivity, we have studied the concentration profile of the submerged block over a large range of surface density {σ} (chains per area) for two different molecular weights. The observed increase in the layer thickness is weaker than the σ1/3 prediction of mean-field and scaling theories for the limiting behavior, but is in agreement with recent numerical self-consistent-field calculations by Whitmore and Noolandi [Macromolecules 23, 3321 (1990)].
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Factor et al. (1993) studied this question.
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