Abstract
Microphase-ordered block copolymers serve as model systems to elucidate the potential of molecular self-assembly and organic templates to fabricate functionalized polymeric materials. Both aspects are related to the incorporation of secondary species such as low-molar-mass compounds or nanoparticles within the copolymer matrices. Since the resulting properties of such functionalized copolymers critically depend on the morphology of the blend or composite, the nonrandom distribution of such inclusions within the copolymer matrix must be understood. Using a self-consistent field theoretical approach, we quantitatively evaluate the segregation and interfacial excess of low-molar-mass and nanoscale species in ordered triblock copolymers as functions of block selectivity and inclusion size. The predictions are found to agree with the morphology observed in a model triblock copolymer/nanoparticle composite, thereby demonstrating the generality of this approach. Our results suggest a wide correspondence in the structure-forming effect of molecular and nanoscale inclusions that will have implications in the design and processing of functional nanostructured polymers.
