Chain Flexibility Effects on the Self-Assembly of Diblock Copolymer in Thin Films

We investigate the effects of chain flexibility on the self-assembly behavior of symmetric diblock copolymers (BCPs) when they are confined as a thin film between two surfaces. Employing worm-like chain (WLC) self-consistent field theory, we study the relative stability of parallel (L parallel to) and perpendicular (L perpendicular to) orientations of BCP lamellar phases, ranging in chain flexibility from flexible Gaussian chains to semiflexible and rigid chains. For flat and neutral bounding surfaces (no surface preference for one of the two BCP components), the stability of the L perpendicular to lamellae increases with chain rigidity. When the top surface is flat and the bottom substrate is corrugated, increasing the surface roughness enhances the stability of the L perpendicular to lamellae for flexible Gaussian chains. However, an opposite behavior is observed for rigid chains, where the L perpendicular to stability decreases as the substrate roughness increases. We further show that as the substrate roughness increases, the critical value of the substrate preference, u*, corresponding to an L perpendicular to-to-L parallel to transition, decreases for rigid chains, while it increases for flexible Gaussian chains. Our results highlight the physical mechanism of tailoring the orientation of lamellar phases in thin-film setups. This is of importance, in particular, for short (semiflexible or rigid) chains that are in high demand in emerging nanolithography and other industrial applications.