Bingyan Wang
(, ), Wenxia Liu
(, ), Zhaoping Song
(, ), Guodong Li
(, ), Dehai Yu
(, ), Xiaona Liu
(, ), Huili Wang
(, ), Shaohua Ge
(, )
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The resultant Ga<sup>3+</sup> ions interact with carboxyl groups in the PAA, forming soft coordination links that enhance the hydrogel’s rapid gelation. The incorporation of VSNPs significantly enhances the hydrogel’s elasticity, toughness, and low-temperature resilience without glycerol. Notably, its intrinsic moldability, adhesion, and self-healing properties are retained. Applied as a strain sensor, this hydrogel demonstrates a high gauge factor (GF) of 17.4, responsive time of 250 ms for both activation and recovery, an ultra-low detection limit of 0.1%, and excellent durability over 800 cycles at 100% strain. Short-term immersion in a glycerol solution (20 min) further augments its stretchability to 2688% and GF to 28.1 across a strain range of 1325%–1450%, broadening its operational ranges to 0–1450% at −18°C. 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Enhanced multifunctional liquid metal-based hydrogels with vinyl silica nanoparticles for advanced strain sensing applications
Conductive hydrogels have garnered considerable interest for their applications in wearable electronic skins, owing to their superior properties. Nevertheless, challenges persist, including low sensitivity, poor cyclic stability, and limited tolerance to extreme conditions. This study develops a novel liquid metal-based conductive hydrogel with a dual cross-linked polyacrylic acid (PAA) matrix, employing both “soft” coordination and “hard” covalent cross-linking mechanisms. This hybrid network is formulated using guar gum (GG)-stabilized gallium (Ga) droplets, which catalyze the copolymerization of vinyl-hybrid silica nanoparticles (VSNPs) and acrylic acid (AA). The resultant Ga3+ ions interact with carboxyl groups in the PAA, forming soft coordination links that enhance the hydrogel’s rapid gelation. The incorporation of VSNPs significantly enhances the hydrogel’s elasticity, toughness, and low-temperature resilience without glycerol. Notably, its intrinsic moldability, adhesion, and self-healing properties are retained. Applied as a strain sensor, this hydrogel demonstrates a high gauge factor (GF) of 17.4, responsive time of 250 ms for both activation and recovery, an ultra-low detection limit of 0.1%, and excellent durability over 800 cycles at 100% strain. Short-term immersion in a glycerol solution (20 min) further augments its stretchability to 2688% and GF to 28.1 across a strain range of 1325%–1450%, broadening its operational ranges to 0–1450% at −18°C. Prolonged exposure (4 h) also improves water retention and high-temperature resistance, making this hydrogel a promising material for sustainable, high-performance wearable electronics.
期刊介绍:
Science China Materials (SCM) is a globally peer-reviewed journal that covers all facets of materials science. It is supervised by the Chinese Academy of Sciences and co-sponsored by the Chinese Academy of Sciences and the National Natural Science Foundation of China. The journal is jointly published monthly in both printed and electronic forms by Science China Press and Springer. The aim of SCM is to encourage communication of high-quality, innovative research results at the cutting-edge interface of materials science with chemistry, physics, biology, and engineering. It focuses on breakthroughs from around the world and aims to become a world-leading academic journal for materials science.