Conventional conductive hydrogels are susceptible to swelling in aquatic environments; which compromises their mechanical integrity; a limitation that poses a potential challenge to their long-term stability and application. In this study, a zwitterionic ion-conductive hydrogel was fabricated from polyvinyl alcohol (PVA), acrylic acid (AA), and [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (SMBA), forming a dual-network structure. A copolymer of zwitterionic SBMA and AA formed the first network, and PVA formed the second network by repeated freeze–thawing. The equilibrium state of zwitterionic SBMA was modulated by AA to protonate the SBMA, which resulted in the conversion of -SO₃⁻ to -SO₃H; thus, hydrogels had the anti-swelling property driven by electrostatic repulsion. In addition, the prepared hydrogels possessed excellent mechanical properties (tensile strength of 0.76 MPa, elongation at break of 322%, and compressive strength of 0.97 MPa at 75% compressive strain) and remarkable anti-swelling properties (80% swelling after 120 h of immersion). Owing to the zwitterionic nature of SBMA, the hydrogel also showed inherent antimicrobial properties and high electrical conductivity, which could be capable of monitoring human movement and physiological signals. This work provides a facile strategy for designing hydrogels with remarkable mechanical properties and anti-swelling characteristics, expanding the application environment of hydrogels in flexible sensing

The development of high-performance sensing materials is critical for advancing bioelectronics. Conductive hydrogels, with their unique flexibility, are promising candidates for biomedical sensors. However, traditional conductive hydrogels often suffer from excessive swelling and undesirable antibacterial activity, limiting their practical use. To overcome these challenges, anti-swelling, antibacterial, and ionically conductive hydrogels were built through free radical polymerization. The preparation was conducted using a monomer mixture comprising acrylic acid (AA), the antibacterial zwitterionic compound [2-(methacryloyloxy)ethyl]dimethyl-(3-sulfopropyl)ammonium hydroxide (SBMA), and the hydrophobic monomer lauryl methacrylate (LMA). The protonation of SBMA by AA enables electrostatic repulsion, thereby imparting anti-swelling properties to the hydrogel. The introduction of hydrophobic LMA components further enhances the anti-swelling and mechanical performance of hydrogel. The resulting hydrogel exhibits excellent anti-swelling property with a swelling ratio of 59.36% after 120 h and good mechanical performance with a tensile strength of 158 kPa, an elongation at break of 176%, and a compressive strength of 0.37 MPa at 80% strain. In addition, hydrogels possess superior sensing performance for strain sensing with a gauge factor of 1.315 within 40–60% of strain, 330 ms of response time, and 177 ms of recovery time. Furthermore, the hydrogel is capable of monitoring human motion and physiological signals. These attributes make it highly suitable for wearable sensors and biomedical monitoring applications.

Self-healing conductive hydrogels have attracted considerable interest in recent research due to their applications in biomedical and electronic fields. The design and preparation of a functional self-healing conductive hydrogel that features multiple stimuli-responsive properties, adhesion, and tunable mechanical characteristics for a wearable electronic sensor is highly anticipated. In this work, we proposed a hydrogel sensor through free radical polymerization by using host molecule acryloyl-β-cyclodextrin (AC-β-CD), guest molecule of acryloyl-1-adamantanamine (AC-AD), N-isopropylacrylamide (NIPAM), and conductive reduced graphene oxide/β-CD (rGO-CD). The chemical and physical structure, conductivity, de-swelling/swelling behavior, photothermal behavior, mechanical performance, adhesive performance, injectable performance, and self-healing performance of the resultant hydrogels were comprehensively investigated. Human motion detection and cytocompatibility test of hydrogel further demonstrated its potential for wearable electronics applications. Overall, this supramolecular conductive hydrogel might open a new sight to develop a multifunctional flexible sensor.