Sticky Rouse Time Features the Self-Adhesion of Supramolecular Polymer Networks

ZQ Shen and HL Ye and QM Wang and M Kroger and Y Li, MACROMOLECULES, 54, 5053-5064 (2021).

DOI: 10.1021/acs.macromol.1c00335

Supramolecular polymers are fascinating materials due to their strikingly self-healing capabilities empowered by reversible bonds. However, due to the lack of knowledge about the molecular structure evolution at the fractured interfaces, there is no existing theory to explain and predict the diverse healing times of different supramolecular materials observed in experiments. Here, we systematically study the self-adhesion of both unentangled and entangled supramolecular polymer networks through molecular simulations. We find that the recovery of macroscopic interfacial strength almost linearly depends on the microscopic molecular formations at fractured interfaces of supramolecular polymers, including reversible bonds and entanglements (entangled systems only). More importantly, we place the healing time into the context of intrinsic relaxation timescales of supramolecular polymer networks. It is found that the intrinsic sticky Rouse time features the self-adhesion process of all fractured supramolecular polymers, representing the full recovery of interfacial strength. At this critical timescale, two things happened to guarantee the full recovery of fractured systems: (i) polymer chains have diffused across the fractured interface with a displacement comparable to their sizes; (ii) the crossed stickers and polymer chains have updated their reversible bonds and entanglements (entangled systems only), respectively. The clear molecular description and suggested characteristic self-adhesion time will help the molecular design of supramolecular polymers.

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