Molecular-weight effects of a homopolymer on the AB- and ABC-stacks of perforations in block copolymer/homopolymer films.

We have demonstrated the molecular-weight effects of adding homopolystyrene (hPS) on the evolution of perforated layers and double gyroids in polystyrene- block -poly(methyl methacrylate)-based films during isothermal annealing. Two homopolystyrenes of 2.8 and 17 kg mol -1 were used. To prepare blend films, PS- b -PMMA and hPS x ( x : 2.8 or 17) were mixed at a weight-fraction ratio of 75/25 in toluene and then spin-coated at SiO x /Si. Spin coating inevitably produced films with thick edges at the periphery of the substrate. The structural evolution of the spun films was in situ characterized by grazing incidence small-angle X-ray scattering (GISAXS). The annealed films were then characterized using a scanning electron microscope (SEM). We found that thin middle regions behaved differently from thick beads for the films. The middle of the blend films mainly formed perforated layers with different spatial orders and orientations, depending on the molecular weight of added hPS chains. Hexagonally perforated layers quickly formed at 205 °C for PS- b -PMMA/hPS 2.8 films. However, when hPS 17 was used instead of hPS 2.8 , perforated layers formed with defects in PS- b -PMMA/hPS 17 films annealed at 205 °C. Annealing at 240 °C improved the spatial order and orientation of perforated layers for a PS- b -PMMA/hPS 17 film. Nevertheless, annealing at 240 °C inversely depressed the in-plane spatial order of perforated layers for a PS- b -PMMA/hPS 2.8 film. The depression in the in-plane spatial order is ascribed to a dilution effect of added short chains. Compared to the middle regions, the thick beads went through several metastable phases, such as perpendicularly oriented perforated layers and double gyroids.