机构:
Korea Res Inst Chem Technol, Res Ctr Green Fine Chem, Ulsan 681310, South KoreaConcordia Univ, Dept Chem & Biochem, Ctr NanoSci Res, Montreal, PQ H4B 1R6, Canada
Noh, Seung Man
[2
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Nam, Joon Hyun
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机构:
Korea Res Inst Chem Technol, Res Ctr Green Fine Chem, Ulsan 681310, South KoreaConcordia Univ, Dept Chem & Biochem, Ctr NanoSci Res, Montreal, PQ H4B 1R6, Canada
Polymer-based crosslinked networks with intrinsic self-repairing ability have emerged due to their built-in ability to repair physical damages. Here, novel dual sulfide-disulfide crosslinked networks (s-ssPxNs) are reported exhibiting rapid and room temperature self-healability within seconds to minutes, with no extra healing agents and no change under any environmental conditions. The method to synthesize these self-healable networks utilizes a combination of well-known crosslinking chemistry: photoinduced thiol-ene click-type radical addition, generating lightly sulfide-crosslinked polysulfide-based networks with excess thiols, and their oxidation, creating dynamic disulfide crosslinkages to yield the dual s-ssPxNs. The resulting s-ssPxN networks show rapid self-healing within 30 s to 30 min at room temperature, as well as self-healing elasticity with reversible viscoelastic properties. These results, combined with tunable self-healing kinetics, demonstrate the versatility of the method as a new means to synthesize smart multifunctional polymeric materials.