Hydrogel electrolytes as soft ionic conductors have been extensively exploited to establish skinlike and biocompatible devices. However, in many common hydrogels, there exists irreversible elongation upon prolonged stretching cycles and poor interfacial contact, which have significantly hindered their practical applications where long-term operation at large deformations is needed. Herein, multifunctional soft electronic devices with reversible stretchability and improved electrode/electrolyte interfaces are demonstrated by employing polyacrylamide-based double-network organohydrogel electrolytes soaked with a high content of tannic acid (TA) that affords multiple noncovalent interactions and redox activity. Performances of the TA-rich gels are evaluated for the first time in realizing shape-recoverable stretchable devices against repeated deformations to 500% strain, with superior gel-electrode interfaces exhibiting both intimate adhesion and boosted electrochemical capacitance of >200 mF·cm-2. A maximal 4-fold higher capacitance can be achieved by introducing TA and ethylene glycol (EG) into hydrogels. Moreover, a soft electronic system consisting of stretchable supercapacitors and gel-based microsensors was demonstrated, in which the electronic performance of these devices can be well preserved after >1000 repeated cycles at strains of up to 200%, without obvious residual strain or electrode delamination. This could pave a route to the design of multifunctional gel networks tackling both the mechanical and interfacial issues in soft and biocompatible devices.
Keywords: electrode/electrolyte interface; organohydrogel electrolyte; self-recovery; stretchable electronics; tannic acid.