Shanghai Key Laboratory of Advanced Polymeric Materials, School of Materials Science and Engineering, East China University of Science and Technology, Shanghai 200237, China
zhangls@ecust.edu.cn
收稿:2026-03-11,
录用:2026-04-07,
网络首发:2026-07-01,
纸质出版:2026-05
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Zhu, Z. P.; Lin, J. P.; Zhang, L. S. Sequence-encoded conformation pathways in viscoelastic microphase separation of multiblock copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3705-7
Zhe-Peng Zhu, Jia-Ping Lin, Liang-Shun Zhang. Sequence-encoded Conformation Pathways in Viscoelastic Microphase Separation of Multiblock Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-13.
Zhu, Z. P.; Lin, J. P.; Zhang, L. S. Sequence-encoded conformation pathways in viscoelastic microphase separation of multiblock copolymers. Chinese J. Polym. Sci. https://doi.org/10.1007/s10118-026-3705-7 DOI:
Zhe-Peng Zhu, Jia-Ping Lin, Liang-Shun Zhang. Sequence-encoded Conformation Pathways in Viscoelastic Microphase Separation of Multiblock Copolymers[J/OL]. Chinese Journal of Polymer Science, 2026, 441-13. DOI: 10.1007/s10118-026-3705-7.
Deciphering how molecular sequences of block copolymers program their self-assembly pathways is a pivotal pursuit in polymer science. To this end
we integrated viscoelastic constitutive relations into dynamic self-consistent field theory (DSCFT) to probe the spatiotemporally coupled evolution of nanostructures and chain conformations in sequence-defined multiblock copolymers during viscoelastic microphase separation. The DSCFT simulations reveal that the linear sequence of slow-relaxing “hard” and fast-relaxing “soft” blocks encodes two programmable kinetic motifs: a hard-soft-hard sequence drives a sharp
droplet-coalescence-triggered conversion from loop to bridge conformations during viscoelasticity-mediated phase inversion
whereas a soft-hard-soft sequence governs a gradual
network-contraction-driven relaxation of chain conformations. Serving as modular kinetic codes identified in the system of triblock copolymers
these kinetic motifs were shown to operate concurrently within tetrablock chains and generalize to penta- and hexa-block architectures
demonstrating the scalability and robustness of sequence-encoded dynamics. This work establishes the paradigm of sequence-encoded viscoelastic kinetics
providing a mechanism for controlling pathway-dependent self-assembly at the molecular level.
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