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Article Abstract

Polymer gels have been widely used in flexible electronics, soft machines and impact protection materials. Conventional gels usually suffer from the inherent conflict between stiffness and toughness, severely hampering their applications. This work proposes a facile yet versatile strategy to break through this trade-off via the synergistic effect of crystal-domain cross-linking and chelation cross-linking, without the need for specific structure design or adding other reinforcements. Both effects are proven to boost the mechanical performance of the originally weak gel, and result in a stiff and tough conductive gel, achieving significant enhancements in elastic modulus and toughness by up to 366-, and 104-folds, respectively. The resultant gel achieves coordinatively enhanced stiffness (110.26 MPa) and toughness (219.93 MJ m), reconciling the challenging trade-off between them. In addition, the presented strategy is found generalizable to a variety of metal ions and polymers, offering a promising way to expand the applicability of gels.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11695677PMC
http://dx.doi.org/10.1038/s41467-024-55245-3DOI Listing

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Polymer gels have been widely used in flexible electronics, soft machines and impact protection materials. Conventional gels usually suffer from the inherent conflict between stiffness and toughness, severely hampering their applications. This work proposes a facile yet versatile strategy to break through this trade-off via the synergistic effect of crystal-domain cross-linking and chelation cross-linking, without the need for specific structure design or adding other reinforcements.

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Coordinatively Stiffen and Toughen Hydrogels with Adaptable Crystal-Domain Cross-Linking.

Adv Mater

March 2023

Beijing National Laboratory for Molecular Sciences, Laboratory of Polymer Physics and Chemistry, CAS Research/Education Center for Excellence in Molecular Sciences, Institute of Chemistry, Chinese Academy of Sciences, Beijing, 100190, China.

Conventional hydrogels usually suffer from the inherent conflict between stiffness and toughness, severely hampering their applications as load-bearing materials. Herein, an adaptable crystal-domain cross-linking design is reported to overcome this inherent trade-off for hydrogels by taking full advantage of both deformation-resisting and energy-dissipating capacities of cross-linking points. Through solvent exchange to homogenize the polymer network, followed by salting out to foster crystallization, a class of sal-exogels with high number densities of uniform crystalline domains embedded in homogeneous networks is constructed.

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