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Synthesis of Monodisperse Cylindrical Nanoparticles via Crystallization-driven Self-assembly of Biodegradable Block Copolymers
Published on: June 20, 2019
Self-assembly of rod-coil diblock copolymers within a rod-selective slit: a dissipative particle dynamics simulation
Jian-Hua Huang1, Ze-Xin Ma, Meng-Bo Luo
1Department of Chemistry, Zhejiang Sci-Tech University , Hangzhou 310018, China.
Abstract:
Dissipative particle dynamics simulations are performed to investigate the self-assembly of rod-coil diblock copolymers R(N(R))C(N-N(R)) within a rod-selective slit. The self-assembled structure of the confined system is sensitively dependent on the rigidity kθ and the fraction fR of the rod block and the slit height H. From the phase diagram of structures with respect to kθ and fR for N = 12 and H = 6, we observe four main structures including disordered cylinder (DC) structure, hexagonally packed cylinders (HPC) perpendicular to the slit surfaces, and lamellar structures parallel (L∥) and perpendicular (L⊥) to surfaces. And structure transitions can be achieved by tuning kθ. The effect of the slit height on the self-assembled structure is also studied for R6C6 and R7C5 copolymers with large kθ. For R6C6, different structures near surfaces and in the interior of slit are observed in relatively wide slits. Whereas for R7C5, L⊥ structure, whose lamellar domain spacing decays exponentially with H, is generally generated. Our results suggest an effective way to control the ordering of rod-coil diblock copolymers under nanoscale confinement.

