Issue 21, 2015

Self-healable, tough and highly stretchable ionic nanocomposite physical hydrogels

Abstract

We present a facile strategy to synthesize self-healable tough and highly stretchable hydrogels. Our design rationale for the creation of ionic cross-linked hydrogels is to graft an acrylic acid monomer on the surface of vinyl hybrid silica nanoparticles (VSNPs) for the growth of poly(acrylic) acid (PAA), and the obtained VSNP–PAA nanobrush can be used as a gelator. Physical cross-linking through hydrogen bonding and ferric ion-mediated ionic interactions between PAA polymer chains of the gelators yielded ionic nanocomposite physical hydrogels with excellent and balanced mechanical properties (tensile strength 860 kPa, elongation at break ∼2300%), and the ability to self-repair (tensile strength ∼560 kPa, elongation at break ∼1800%). The toughness and stretchability arise from the reversible cross-linking interactions between the polymer chains that help dissipate energy through stress (deformation) triggered dynamic processes. These unique properties will enable greater application of these hydrogel materials, especially in tissue engineering.

Graphical abstract: Self-healable, tough and highly stretchable ionic nanocomposite physical hydrogels

Supplementary files

Article information

Article type
Paper
Submitted
28 Feb 2015
Accepted
08 Apr 2015
First published
09 Apr 2015

Soft Matter, 2015,11, 4235-4241

Author version available

Self-healable, tough and highly stretchable ionic nanocomposite physical hydrogels

M. Zhong, X. Liu, F. Shi, L. Zhang, X. Wang, A. G. Cheetham, H. Cui and X. Xie, Soft Matter, 2015, 11, 4235 DOI: 10.1039/C5SM00493D

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