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Updated: Nov 23, 2025

Self-assembling Morphologies Obtained from Helical Polycarbodiimide Copolymers and Their Triazole Derivatives
Published on: February 7, 2017
Transformable Colloidal Polymer Particles with Ordered Internal Structures
Renhua Deng1, Lingfei Zheng2, Xi Mao1
1State Key Laboratory of Materials Processing and Die & Mould Technology, Key Laboratory of Material Chemistry for Energy Conversion and Storage of Ministry of Education (HUST), School of Chemistry and Chemical Engineering, Huazhong University of Science and Technology (HUST), Wuhan, 430074, China.
Abstract:
Based on studies combining experiments and simulations, internally ordered colloidal particles that are able to undergo morphological transformations both in shape and internal structure are presented. The particles are prepared by emulsion solvent evaporation-induced 3D soft confined assembly of di-block copolymer polystyrene-block-poly(4-vinylpyridine) (PS-b-P4VP). Control over the solvent selectivity leads to a dramatic change in shape and internal structure for particles. Pupa-like particles of lamellar morphology are obtained when using a non-selective solvent, while patchy particles possessing a plum pudding structure formed when the solvent is selective for PS-block. More interestingly, 3D soft confined annealing drives order-order morphological transformation of the particles. The morphology of reshaped particles can be well controlled by varying the solvent selectivity, annealing time, and interfacial interaction. The experimental results can be explained based on simulations. This study can offer considerable scope for the design of new stimuli-responsive colloidal particles for potential applications in photonic crystal, drug delivery and release, sensor and smart coating, etc.
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