Soft electronics are rising electronic technologies towards applications spanning from healthcare monitoring to medical implants. However, poor adhesion strength and significant mechanical mismatches inevitably cause the interface failure of devices. Herein we report a self-adhesive conductive polymer that possesses low modulus (56.1-401.9 kPa), high stretchability (700%), high interfacial adhesion (lap-shear strength >1.2 MPa), and high conductivity (1-37 S/cm). The self-adhesive conductive polymer is fabricated by doping the poly(3,4-ethylenedioxythiophene): poly(styrene sulfonate) composite with a supramolecular solvent (β-cyclodextrin and citric acid). We demonstrated the solution process-based fabrication of self-adhesive conductive polymer-based electrodes for various soft devices, including alternating current electroluminescent devices, electromyography monitoring, and an integrated system for the visualization of electromyography signals during muscle training with an array of alternating current electroluminescent devices. The self-adhesive conductive polymer-based electronics show promising features to further develop wearable and comfortable bioelectronic devices with the physiological electric signals of the human body readable and displayable during daily activities.

Liquid metal (LM)-based elastomers have received growing interest for wide ranges of applications spanning from soft robotics to flexible electronics. However, the fabrication of multifunctional LM-based elastomer, in particular, featuring...

Textile-based wearable electronics, integrating the functions of electronics into the daily textiles, offers a comfortable interaction between humans and electronic devices. Production of highly conductive and environmentally stable textiles is the precondition for the ultimate wearable electronic system. However, due to the complicated porous structure, it is still technically challenging to endow textiles with desirable conductivity and stability, especially in the case of stretchable fabrics. Herein, we report a facile but effective fabrication strategy combining the electroless deposition and electrodeposition techniques for the metallization of stretchable knitted fabrics. The electroless deposition process first introduces a thin metal layer and yields electrically conductive fabrics. The subsequent electrodeposited metals conformally coat on individual fibers of fabrics, which significantly improves the electrical conductivity, mechanical durability, and environmental stability of metallized textiles. Remarkably, the sheet resistance of metallized textiles reaches less than 0.02 Ω sq–1 and remains relatively stable under more than 400% tensile strain. More importantly, the metallized stretchable fabrics exhibit superior stability when monitored in varied environments for 30 days, further promoting their practical uses in wearable electronics. Finally, a wearable heater and a strain sensor are demonstrated to show potential applications of metallized textiles for personal healthcare and human motion monitoring.

Liquid metal (LM)–polymer composites that combine the thermal and electrical conductivity of LMs with the shape-morphing capability of polymers are attracting a great deal of attention in the fields of reconfigurable electronics and soft robotics. However, investigation of the synergetic effect between the shape-changing properties of LMs and polymer matrices is lacking. Herein, a self-healable and recyclable dual-shape memory composite, comprising an LM (gallium) and a Diels–Alder (DA) crosslinked crystalline polyurethane (PU) elastomer, is reported. The composite exhibits a bilayer structure and achieves excellent shape programming abilities, due to the phase transitions of the LM and the crystalline PU elastomers. To demonstrate these shape-morphing abilities, a heat-triggered soft gripper, which can grasp and release objects according to the environmental temperature, is designed and built. Similarly, combining the electrical conductivity and the dual-shape memory effect of the composite, a light-controlled reconfigurable switch for a circuit is produced. In addition, due to the reversible nature of DA bonds, the composite is self-healable and recyclable. Both the LM and PU elastomer are recyclable, demonstrating the extremely high recycling efficiency (up to 96.7%) of the LM, as well as similar mechanical properties between the reprocessed elastomers and the pristine ones.

Organohydrogels with distinct antifreezing and antidehydration properties have aroused great interest among researchers, and various organohydrogels and organohydrogel-based applications have emerged recently. There are two popular synthesis strategies to prepare these antifreezing and antidehydration organohydrogels: the in-situ gelling and the solvent displacement strategies. Although both strategies have been widely applied, there is a lack of comparative study of these two strategies. In this work, to elucidate the comparative advantages of the two synthesis strategies, we studied and compared the mechanical and environmental tolerant properties of the organohydrogels synthesized from both strategies. The glycerol-based and ethylene glycol-based chemical polyacrylamide (PAAm) organohydrogel and the glycerol-based physical gelatin organohydrogel were synthesized and studied. Through the comparative study, we have found that the organohydrogels from different strategies with the same dispersion medium showed similar antifreezing and antidehydration properties but different mechanical properties. The mechanical properties of these organohydrogels are influenced by two opposite factors for each strategy: the enhanced physical interactions induced strengthening and solvent effect or swelling induced weakening. We hope this study may provide a better understanding of the synthesis strategies of organohydrogels and provide a valuable guide to choose the suitable synthesis strategy for each application.

Adhesion and spreading of liquid metals (LMs) on substrates are essential steps for the generation of flexible electronics and thermal management devices. However, the controlled deposition is limited by the high surface tension and peculiar wetting and adhesion behavior of LMs. Herein, we introduce gelatin-regulated LM droplet deposition and sintering (GLMDDS), for the upscalable production of conformally adhesive, solidlike, yet transient LM thin films and patterns on diverse substrates. This method involves four steps: homogeneous deposition of LM microdroplets, gelation of the LM-gelatin solution, toughening of the gelatin hydrogel by solvent displacement, and peeling-induced sintering of LM microdroplets. The LM thin film exhibits a three-layer structure, comprising an LM microdroplet-embedded tough organohydrogel adhesion layer, a continuous LM layer, and an oxide skin. The composite exhibits high stretchability and mechanical robustness, conformal adhesion to various substrates, high conductivity (4.35 × 105 S·m–1), and transience (86% LM recycled). Large-scale deposition (i.e., 5.6 dm2) and the potential for patterns on diverse substrates demonstrate its upscalability and broad suitability. Finally, the LM thin films and patterns are applied for flexible and wearable devices, i.e., pressure sensors, heaters, human motion tracking devices, and thermal management devices, illustrating the broad applicability of this strategy.