Solvent selectivity governs the emergence of temperature responsiveness in block copolymer self-assembly
Autor: | Remco Tuinier, Paul J. Hurst, A. Catarina C. Esteves, Alessandro Ianiro, Michael Sztucki, Joseph P. Patterson, Marco M. R. M. Hendrix, Mark Vis |
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Přispěvatelé: | Physical Chemistry, Self-Organizing Soft Matter, Materials and Interface Chemistry, ICMS Core |
Jazyk: | angličtina |
Rok vydání: | 2021 |
Předmět: |
Materials science
Polymers and Plastics Polymers 02 engineering and technology 010402 general chemistry 01 natural sciences Article law.invention Inorganic Chemistry Colloid Engineering law Phase (matter) Materials Chemistry Copolymer Crystallization chemistry.chemical_classification Organic Chemistry Polymer 021001 nanoscience & nanotechnology 0104 chemical sciences Solvent Chemical engineering chemistry Chemical Sciences Self-assembly 0210 nano-technology Selectivity |
Zdroj: | 'Macromolecules ', vol: 54, pages: 2912-2920 (2021) Macromolecules, vol 54, iss 6 Macromolecules Macromolecules, 54(6), 2912-2920. American Chemical Society |
ISSN: | 0024-9297 |
Popis: | In highly selective solvents, block copolymers (BCPs) form association colloids, while in solvents with poor selectivity, they exhibit a temperature-controlled (de)mixing behavior. Herein, it is shown that a temperature-responsive self-assembly behavior emerges in solvent mixtures of intermediate selectivity. A biocompatible poly-ethylene(oxide)-block-poly-ϵ-caprolactone (PEO-PCL) BCP is used as a model system. The polymer is dissolved in solvent mixtures containing water (a strongly selective solvent for PEO) and ethanol (a poorly selective solvent for PEO) to tune the solvency conditions. Using synchrotron X-ray scattering, cryogenic transmission electron microscopy, and scanning probe microscopy, it is shown that a rich temperature-responsive behavior can be achieved in certain solvent mixtures. Crystallization of the PCL block enriches the phase behavior of the BCP by promoting sphere-to-cylinder morphology transitions at low temperatures. Increasing the water fraction in the solvent causes a suppression of the sphere-to-cylinder morphology transition. These results open up the possibility to induce temperature-responsive properties on demand in a wide range of BCP systems. |
Databáze: | OpenAIRE |
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