Tough self-healing elastomers by molecular enforced integration of covalent and reversible networks
Jinrong Wu, Li-Heng Cai, and David A. Weitz

TL;DR
This paper introduces a novel hybrid polymer network that combines covalent and reversible bonds at the molecular level, resulting in tough, self-healing elastomers with high fracture energy and room-temperature healing capabilities.
Contribution
The authors develop a new method to integrate covalent and reversible bonds in dry elastomers without co-solvents, enhancing toughness and self-healing performance.
Findings
Fracture energy of 13,500 J/m^2 comparable to natural rubber
Self-heals at room temperature with 4 MPa tensile strength
Molecular-level mixing of bonds improves mechanical properties
Abstract
Self-healing polymers crosslinked by solely reversible bonds are intrinsically weaker than common covalently crosslinked networks. Introducing covalent crosslinks into a reversible network would improve mechanical strength. It is challenging, however, to apply this design concept to dry elastomers, largely because reversible crosslinks such as hydrogen bonds are often polar motifs, whereas covalent crosslinks are non-polar motifs, and these two types of bonds are intrinsically immiscible without co-solvents. Here we design and fabricate a hybrid polymer network by crosslinking randomly branched polymers carrying motifs that can form both reversible hydrogen bonds and permanent covalent crosslinks. The randomly branched polymer links such two types of bonds and forces them to mix on the molecular level without co-solvents. This allows us to create a hybrid dry elastomer that is very…
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