This work demonstrates enhanced mechanical properties in bioinspired hydrogels, suggesting they can function as durable strain sensors under cyclic deformation.
Living organisms exhibit exceptional mechanical adaptability under external stresses by integrating hierarchical inorganic-organic structures. Inspired by their biomineralization, this study presents a synthetic strategy to fabricate mechanically reinforced, hyperelastic, mineralized hydrogels via in situ silicification. Based on the natural bio-silicification process, we first mineralize silica nanoparticles from a nanocomplex containing high amounts of amine moieties in the hydrogel matrix. The size, shape, and distribution of silica nanoparticles were adjustable through the consecutive in situ process, which enables interlocking/entrapment of silica nanoparticles and polymer networks. The resulting silicified hydrogels overcome the conventional trade-off between strength/stiffness and toughness, thereby achieving the enhanced mechanical properties with hysteresis-free and deformation-rate-independent hyperelastic behaviors. Their superior mechanical characteristics allow the hydrogel to function as a strain sensor with exceptional durability under cyclic loading-unloading deformation. This strategy offers a versatile platform for the design of mechanically robust hydrogels.
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Kim et al. (2025) studied this question.
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