Ionogels with self-healing properties have become more
and more
desirable because they can improve the reliability, safety, and fatigue-resistant
performance of flexible devices. However, the self-healing property
of ionogels is usually susceptible to water molecules, and the application
of ionogel sensors is limited to the atmospheric environment. Inspired
by gelatinous jellyfish, herein, an underwater self-healing ionogel
was prepared via one-step photoinitiated polymerization of acrylic
acid 2,2,2-trifluoroethyl ester and N-isopropylacrylamide (NIPAm)
in a hydrophobic ionic liquid 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide
([EMIm][TFSI]). The dynamic physical interactions (hydrogen bonding
and ion–dipole interactions) endowed the ionogel with remarkable
transparency, underwater self-healing (up to 96%), toughness (3.93
MJ m–3), and underwater adhesion. And the cross-linking
ionogel could be green recycled by ethanol for further application.
Especially, the ionogel-based sensor presented excellent strain and
pressure sensing sensitivity, rapid responsiveness (140 ms), and ultrastability.
The ionogel could be further assembled into an optical camouflage
sensor to detect and distinguish different human motions in real time
with high sensitivity, stability, and repeatability, as well as for
underwater electrocardiography monitoring wirelessly. This ionogel
provides a promising strategy for the development of underwater self-healing
sensors.