Conductive hydrogels are promising for wearable electronics and biomedicine due to their flexibility, biocompatibility, and tunable conductivity, but synergizing high conductivity, robust mechanics, and tissue adhesion remains challenging. Herein, a novel stretchable, dual-conductive, self-adhesive poly(2-hydroxyethyl methacrylate)-MXene-Ca 2+ (pMC) hydrogel was fabricated via facile physical crosslinking. The underlying mechanism involves a dynamic non-covalent network, where reversible hydrogen bonds within pHEMA chains and Ca²⁺-mediated coordination bonds bridging pHEMA and MXene collectively dissipate energy during deformation. This process confers outstanding stretchability and enables reliable self-adhesion through strong interfacial bonding with tissues. Furthermore, synergistic ionic conduction from Ca 2+ transport in pHEMA hydrophilic channels and electronic conduction through a percolating MXene network achieves optimal conductivity of 1.02 S/m under deformation. This synergistic mechanism enables high-fidelity monitoring of human physiological signals, ranging from large-scale joint movements to subtle arterial pulses, with long-term stability of 2,800 s. A sandwich-structured 4-channel electrode array was developed for high-performance electromyography (EMG) and electrocardiography (ECG) acquisition. The array exhibits superior performance over commercial Ag/AgCl electrodes with a signal-to-noise ratio of 21.9, lower skin-electrode impedance, and reliable electrocardiography recording stability over 3,800 s. Combining scalable fabrication, excellent biocompatibility, and synergistic multifunctionality, the pMC hydrogel holds great promise for next-generation wearable bioelectronics in health monitoring and human-machine interfaces. Fabrication of the pHEMA–MXene–Ca²⁺ (pMC) conductive hydrogel and its application in real-time monitoring of human movement and physiological signals (ECG, EMG, finger and knee bending).
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Xue et al. (2026) studied this question.
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