Abstract

Flexible ionic conductors hold significant promise for advancing the field of soft ion electronics in the future. However, the creation of flexible conductors that possess mechanical robustness, underwater adhesion and underwater motion monitoring remains a challenge. Drawing inspiration from the multiphase hetero structure found in biological connective tissues, such as high modulus fibers and low modulus water-rich matrices, this article proposes a one-pot polymerization in-situ design strategy to create a hydrophobic ionogel with a hetero structure of soft and hard domains. The mechanical robustness, elasticity, and toughness of the ionogel are achieved through a synergistic combination of a strong skeleton in the hard domain and an elastic matrix in the soft domain. Additionally,hydrophobic aromatic rings and quaternary ammonium cation simulated cation-π interactions in mussel foot silk protein. Upon contact with water, the hydrophobic clusters quickly aggregate, facilitating the expulsion of interfacial water and exposing salicylic acid groups and quaternary ammonium cationic groups, leading to outstanding underwater adhesion between the ionogel and various substrates. The resulting hydrophobic ionogel can be utilized in underwater wearable electronic devices for monitoring human movement and physiological information, underwater repair monitoring, and intelligent soft robotics, demonstrating its vast potential in the field of underwater sensors.

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