Bioinspired hydrogels are complex materials with distinctive properties comparable to biological tissues. Their exceptional sensitivity to various external stimuli leads to substantial application potential in wearable smart devices. However, these multifaceted hydrogels are often challenging to be combined with pattern customization, stimulus responsiveness, self-healing, and biocompatibility. Herein, inspired by mussel secretions, a printable, self-healing, and biocompatible MXene-based composite hydrogel was designed and prepared by incorporating Ti 3 C 2 T x MXene nanosheets into the hydrogel framework through the chelation of calcium ions (Ca 2+ ) with polyacrylic acid and cellulose nanofibers at alkaline conditions. The biocompatible conductive hydrogel exhibited sensitivity (gauge factor of 2.16), self-healing (within 1 s), recognition, and adhesion, distinguishing it as an ideal candidate for wearable multifunctional sensors toward strain sensing, vocal sensing, signature detection, and Morse code transmission. Additionally, the multifunctional hydrogel manifested efficient electromagnetic interference shielding properties (reaching more than 30 dB at a thickness of 2.0 mm), protecting electronics and humans from electromagnetic radiation and pollution. Therefore, the presented work represents a versatile strategy for developing environmentally friendly conductive hydrogels, demonstrating the perspectives of intelligent hydrogels for multifunctional applications.

Hydrogels of flexibility, strength, and conductivity have demonstrated broad applications in wearable electronics and soft robotics. However, it is still a challenge to fabricate conductive hydrogels with high strength massively and economically. Herein, a simple strategy is proposed to design a strong ionically conductive hydrogel. This ion-conducting hydrogel was obtained under the synergistic action by salting out the frozen mixture of polyvinyl alcohol (PVA) and graphene oxide (GO) using a high concentration of sodium chloride solution. The developed hydrogel containing only 5 wt% PVA manifests good tensile stress (65 kPa) and elongation (180%). Meanwhile, the PVA matrix doped with a small amount of GO formed uniformly porous ion channels after salting out, endowed the PVA/GO hydrogel with excellent ionic conductivity (up to 3.38 S m⁻¹). Therefore, the fabricated PVA/GO hydrogel, anticipated for a strain sensor, exhibits good sensitivity (Gauge factor = 2.05 at 100% strain), satisfying working stability (stably cycled for 10 min), and excellent recognition ability. This facile method to prepare conductive hydrogels displays translational potential in flexible electronics for engineering applications.