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Emergence of layered nanoscale mesh networks through intrinsic molecular confinement self-assembly
- Publication Year :
- 2022
- Publisher :
- American Chemical Society (ACS), 2022.
-
Abstract
- Block copolymer self-assembly is a powerful tool for 2D nanofabrication; however, its extension to complex 3D network structures, which would be useful for a range of applications, is limited. Here, we report a simple method to generate unprecedented 3D mesh morphologies through intrinsic molecular confinement self-assembly. We designed triblock bottlebrush polymers with two Janus domains: one perpendicular and one parallel to the polymer backbone. The former enforces a lamellar superstructure that intrinsically confines the intra-layer self-assembly of the latter, giving rise to a mesh-like monoclinic M15 network substructure with excellent long-range order. Dissipative particle dynamics simulations show that the spatial constraints exerted on the polymer backbone drive the emergence of M15, as well as a tetragonal T131 in the strong segregation regime. This work demonstrates intrinsic molecular confinement as a path to bottom-up assembly of new geometrical phases of soft matter, extending the capabilities of block copolymer nanofabrication.
Details
- Database :
- OpenAIRE
- Accession number :
- edsair.doi.dedup.....99a9bf68b826e635cecac3c5a4016e26