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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Continuous glucose monitors (CGMs), used by patients with diabetes mellitus, can autonomously track fluctuations in blood glucose over time. However, the signal produced by CGMs during the initial recording period following sensor implantation contains substantial noise, requiring frequent recalibration via fingerprick tests. Here, we show that coating the sensor with a zwitterionic polymer, found via a combinatorial-chemistry approach, significantly reduces signal noise and improves CGM performance. We evaluated the polymer-coated sensors in mice as well as in healthy and diabetic non-human primates, and show that the sensors accurately record glucose levels without the need for recalibration. We also show that the polymer-coated sensors significantly abrogated immune responses to the sensor, as indicated by histology, fluorescent whole-body imaging of inflammation-associated protease activity, and gene expression of inflammation markers. The polymer coating may allow CGMs to become standalone measuring devices.

Flexible capacitive pressure sensors with simple structure and low power consumption have attracted great interest because of their promising applications in wearable electronics. However, assembling a pressure sensor with high sensitivity, low detection limit, and wide dynamic range is still a big challenge. Here, a sandwich‐like, flexible capacitive pressure sensor is reported with micropyramid array electrode and porous dielectric layer. Under external stimulus pressure, the distance between two electrodes, and dielectric constant of dielectric layer will change simultaneously, resulting in high sensitivity (2.51 kPa−1) of the sensor. Due to the micropyramid array electrode, the sensor exhibits low detection limit (2.0 Pa), fast response speed (84 ms), wide working range (>10 kPa), and high stability (>5000 dynamic cycles). Finite‐element analysis also reveals that the larger duty ratio and altitude of micropyramid arrays lead to higher sensor sensitivity. By depicting the deformation of micropyramid during compression, the sensing mechanism of these sensors is discovered, providing a potential direction for developing sensitivity and linear range. Additionally, the sensor has been demonstrated to be efficient in monitoring human motion, such as muscle activation and rope skipping, showing high potential in the field of sport wearable equipment.

Multiple stretchable materials have been successively developed and applied to wearable devices, soft robotics, and tissue engineering. Organohydrogels are currently being widely studied and formed by dispersing immiscible hydrophilic/hydrophobic polymer...