Ultra-stretchable, robust, self-healable conductive hydrogels enabled by the synergistic effects of hydrogen bonds and ionic coordination bonds toward high-performance e-skins

Abstract

Ionic conductive hydrogels as electronic skins (e-skins) have showcased pivotal potentials in the realm of human health monitoring and human–machine interfaces. However, developing intelligent hydrogel with remarkable stretchability and mechanical elasticity is yet challenging. Herein, high-performance ion-conducting hydrogels with unprecedented mechanical properties and good transparent, conductive, self-healing properties are constructed via free-radical polymerization of acrylic acid (AA) within the polyvinyl alcohol (PVA) network, and the subsequent freeze–thaw (F-T) treatment and Zr 4+ ion immersion crosslinking technique. Profiting from the synergy of multiple intermolecular/intramolecular hydrogen bonds between different polymers and coordination bonds of carboxyl-Zr 4+ , the resultant PVA/PAA/Zr 4+ hydrogel exhibits high transparency (∼97 %), superior conductivity (0.6089 S/m), a long elongation at break (2053 %), robust self-healing efficiency (96.3 %), high deformation-tolerate property, and notable mechanical repeatability. These multifaceted attributes render the hydrogel to serve as an ionic conductor for capacitive/resistive −type strain sensor. The hydrogel-based resistive-type strain sensor features a wide detection range (0.5 %-800 %), rapid response time (150 ms), long-term stability, and consistent output stability, making it promising in monitoring diverse human motions and seamless human–machine interactions. Additionally, the hydrogel sensor demonstrates excellent linear response in ultra-wide range (0–900 % strain), high sensitivity, and excellent cycling stability in a capacitive mode, enabling to be used for accurately detecting the weights of objects. As such, this work advances the development of ionic conductive hydrogel as flexible and wearable electronic devices.

Topics & Concepts