Transition Pathway between Gyroid and Cylindrical Morphology in Linear Triblock Terpolymer Thin Films

A new transition between alternating gyroid ( G A ) structure and cylindrical morphology was observed in thin films for a poly(isoprene- block -styrene- block -(2-vinylpyridine)) (ISP) triblock terpolymer (I/S/P volume fraction = 0.20:0.66:0.14) exhibiting in bulk a Q 214 (space group I 4 1 32) morphology. Thin films were organized using solvent vapor annealing (SVA) and characterized by atomic force microscopy, transmission electron microscopy, and grazing-incidence small-angle X-ray scattering, coupled with several selective revealing methods adapted to the ISP system. After a short SVA time, the bulk morphology was reproduced with the (011) plane parallel to the surface. With a longer annealing time, a P 2 mm structure with cylindrical polyisoprene (PI) and poly(2-vinylpyridine) (P2VP) domains was obtained. Evidence of domains in transition between gyroid and cylinders was found, suggesting an epitaxial relationship between these two structures. In contrast to the well-known double gyroid ( G D ) to hexagonal (HEX) transition where {121} planes of the G D structure are epitaxially related to the {100} planes of the HEX phase and cylinders grow along the ⟨111⟩ direction, we showed that the {011} planes of the G A phase become the {001} planes of the cylindrical structure ( P 2 mm ) and the cylinders grow along the ⟨010⟩ direction of the G A, parallel to the substrate. This was directly related to the three-dimensional topology of the PI and P2VP networks.