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Transient Colloid Assembly by Fuel-Driven Modulation of Depletion Interactions

preprint
submitted on 27.10.2020, 20:20 and posted on 29.10.2020, 07:16 by Michelle van der Helm, Chang-Lin Wang, Reece Lewis, Sarah Schyck, Laura Rossi, Rienk Eelkema
In biology, energy stored in chemical fuels is used to drive processes energetically uphill, enabling the highly dynamic behavior of living organisms. The out-of-equilibrium behavior can propagate from molecular reaction networks to the micro- and macroscopic scale. These natural phenomena have sparked the design of man-made out of equilibrium chemical reaction networks (CRNs) and dissipative assembly systems with hydrogels, (supra)polymers, vesicles/micelles and colloids. In colloidal systems, the assembly process is typically controlled by balancing the interaction forces. Here, we use a polymeric depletant integrated in a fuel driven esterification CRN to induce transient colloidal assembly. The polymer undergoes a temporal coil-globule transition upon acetylation by the chemical fuel. In the random coil conformation it acts as depletant agent for the silica colloids, promoting colloidal aggregation. As compact globule, the polymer loses its
depletant characteristics. During the fuel cycle the polymer cyclically transitions from one form to the other, directly influencing colloidal aggregation and redispersion. Thus, a fuel-driven CRN on the molecular scale results in a microscopic response with a transient colloidal depletion cycle. Overall, the time-dependent propagation of out-of-equilibrium activity across length scales presented here, offers opportunities to design responsive materials with life like properties.

Funding

ERC consolidator grant 726381

History

Email Address of Submitting Author

r.eelkema@tudelft.nl

Institution

Delft University of Technology

Country

Netherlands

ORCID For Submitting Author

0000-0002-2626-6371

Declaration of Conflict of Interest

declared none

Version Notes

pre-submission version

Licence

Exports