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Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
A simulation study on the self-assembly of rod-coil-rod triblock copolymers within nanoslits
Ze-Xin Ma1, Jian-Hua Huang, Meng-Bo Luo
1Department of Chemistry, Zhejiang Sci-Tech University, Hangzhou 310018, China. jhhuang@zstu.edu.cn.
Abstract:
Self-assembly of rod-coil-rod R4C12R4 triblock copolymers within a nanoslit is investigated by using dissipative particle dynamics simulations. Perpendicular lamellae (L⊥) in nonselective or weak selective slits and parallel lamellae (L∥) in coil-selective slits are observed, and both are almost independent of the slit thickness. However, in the rod-selective slits, the assembled structures are strongly dependent on the slit thickness. With an increase in the slit thickness, we sequentially observe hexagonally packed cylinders (HC) of rod blocks perpendicular to surfaces in thin slits, parallel wavy lamellae, orderly packed alternating cylinders in moderate slits, a mixture structure of HC near surfaces and L⊥ in the interior region, and finally L∥ in wide slits. Our simulation results reveal that the rod block and surface properties play an important role in the assembly of confined rod-coil-rod triblock copolymers. Results also illustrate the competition between the slit thickness and the length scale of lamellae in bulk for the confined copolymers in nanoslits.

