A facile solvent-exchange strategy is devised to fabricate anti-drying, self-healing and transparent organohydrogels for stretchable humidity sensing applications.

Ionic hydrogels, a class of intrinsically stretchable and conductive materials, are widely used in soft electronics. However, the easy freezing and drying of water-based hydrogels significantly limit their long-term stability. Here, a facile solvent-replacement strategy is developed to fabricate ethylene glycol (Eg)/glycerol (Gl)-water binary antifreezing and antidrying organohydrogels for ultrastretchable and sensitive strain sensing within a wide temperature range. Because of the ready formation of strong hydrogen bonds between Eg/Gl and water molecules, the organohydrogels gain exceptional freezing and drying tolerance with retained deformability, conductivity, and self-healing ability even stay at extreme temperature for a long time. Thus, the fabricated strain sensor displays a gauge factor of 6, which is much higher than previously reported values for hydrogel-based strain sensors. Furthermore, the strain sensor exhibits a relatively wide strain range (0.5−950%) even at −18 °C. Various human motions with different strain levels are monitored by the strain sensor with good stability and repeatability from −18 to 25 °C. The organohydrogels maintained the strain sensing capability when exposed to ambient air for nine months. This work provides new insight into the fabrication of stable, ultrastretchable, and ultrasensitive strain sensors using chemically modified organohydrogel for emerging wearable electronics.

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Fabrication of stretchable chemical sensors becomes increasingly attractive for emerging wearable applications in environmental monitoring and health care. Here, for the first time, chemically derived ionic conductive polyacrylamide/carrageenan double-network (DN) hydrogels are exploited to fabricate ultrastretchable and transparent NO 2 and NH 3 sensors with high sensitivity (78.5 ppm −1 ) and low theoretical limit of detection (1.2 ppb) in NO 2 detection. The hydrogels can withstand various rigorous mechanical deformations, including up to 1200% strain, large-range flexion, and twist. The drastic mechanical deformations do not degrade the gas-sensing performance. A facile solvent replacement strategy is devised to partially replace water with glycerol (Gly) molecules in the solvent of hydrogel, generating the water−Gly binary hydrogel with 1.68 times boosted sensitivity to NO 2 and significantly enhanced stability. The DN-Gly NO 2 sensor can maintain its sensitivity for as long as 9 months. The high sensitivity is attributed to the abundant oxygenated functional groups in the well-designed polymer chains and solvent. A gas-blocking mechanism is proposed to understand the positive resistance shift of the gas sensors. This work sheds light on utilizing ionic conductive hydrogels as novel channel materials to design highly deformable and sensitive gas sensors.

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