Multi-characteristic tannic acid-reinforced polyacrylamide/sodium carboxymethyl cellulose ionic hydrogel strain sensor for human-machine interaction.

Big data and cloud computing are propelling research in human-computer interface within academia. However, the potential of wearable human-machine interaction (HMI) devices utilizing multiperformance ionic hydrogels remains largely unexplored. Here, we present a motion recognition-based HMI system that enhances movement training. We engineered dual-network PAM/CMC/TA (PCT) hydrogels by reinforcing polyacrylamide (PAM) and sodium carboxymethyl cellulose (CMC) polymers with tannic acid (TA). These hydrogels possess exceptional transparency, adhesion, and remodelling features. By combining an elastic PAM backbone with tunable amounts of CMC and TA, the PCT hydrogels achieve optimal electromechanical performance. As strain sensors, they demonstrate higher sensitivity (GF = 4.03), low detection limit (0.5 %), and good linearity (0.997). Furthermore, we developed a highly accurate (97.85 %) motion recognition system using machine learning and hydrogel-based wearable sensors. This system enables contactless real-time training monitoring and wireless control of trolley operations. Our research underscores the effectiveness of PCT hydrogels for real-time HMI, thus advancing next-generation HMI systems.

Tunable mechanical, self-healing hydrogels driven by sodium alginate and modified carbon nanotubes for health monitoring.

Conductive hydrogels featuring a modulus similar to the skin have flourished in health monitoring and human-machine interface systems. However, developing conductive hydrogels with self-healing and tunable force-electrical performance remains a problem. Herein, a hydrogen bonding cross-linking strategy was utilized by incorporating silk sericin-modified carbon nanotubes (SS@CNTs) into sodium alginate (SA) and polyvinyl alcohol (PVA). Hydrogels synthesized with desirable tensile strength and self-healing ability (67.2 % self-healing efficiency in fracture strength) assembled into strain sensors with a low detection limit of 0.5 % and a gauge factor (GF) of 4.75 (0-17 %). Additionally, as-prepared hydrogels exhibit high sensitivity to tiny pressure changes, allowing recognition of complex handwriting. Notably, resulting hydrogels possess self-powered property, generating up to 215 V and illuminating 100 commercial green LEDs. This work stems from the pressing need for multifunctional hydrogels with prospective applications in human motion sensing and energy harvesting.