ArticleAdvanced materials (Deerfield Beach, Fla.)2026
Harnessing Chain Mobility via Protonation for Tough and Isotropic Hydrogel.
Article in Advanced materials (Deerfield Beach, Fla.), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.
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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.
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Who cites it
1 citing paper in PubMed.
- Strengthening Constitutive Motifs in Isotropic Fibrous Hydrogel for Exceptional Damage Resistance.Advanced science (Weinheim, Baden-Wurttemberg, Germany) · 2026Article
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Authors and funding
15 authors.
Funding
Abstract
Fabricating hydrogels with isotropically high tensile strength, stretchability, and toughness is crucial for applications in tissue engineering, stretchable bioelectronics and soft robots. However, many toughening strategies, including mechanical training, directional freezing, and solvent exchange, often induce anisotropy or fail to enhance all these metrics simultaneously. Herein, we report a strategy to fabricate ultra-tough, isotropic poly(vinyl alcohol) (PVA) hydrogels by synergistically modulating polymer chain mobility and physical crosslinking through sequential acidification, freeze-thawing, and salting-out. Acidification protonates the hydroxyl groups, suppressing premature interchain hydrogen bonding and promoting network homogenization. Subsequent salting-out deprotonates the hydroxyl groups to strengthen the interpolymer hydrogen bonds, forming crystalline domains that act as strong, reversible physical crosslinks. The resulting hydrogel achieves a high tensile strength of 29.5 MPa, stretchability of 2683%, and record-high toughness of 424 MJ m
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