Demonstrates improved biocompatibility and tissue adhesion in supercapacitors, indicating potential for biomedical applications.
A self ‑ adhesive supercapacitor is developed based on a biocompatible hydrogel matrix integrated with poly(3, 4 ‑ ethylenedioxythiophene): poly(styrene sulfonate) as the conductive material. For biomedical devices, achieving stable adhesion to dynamic biological tissues is a key challenge. To address this, an integrated structure is created through the in situ polymerization of poly (3, 4 ‑ ethylenedioxythiophene): poly(styrene sulfonate) on a hydrogel composite composed of polyacrylamide, polydopamine, and quaternary ammonium salt of chitosan. This method eliminates interfacial resistance and enhances mechanical stability. The hydrogel matrix is optimized with 20% acrylamide, and the conductive polymer is polymerized for 36 h, yielding a specific capacitance of 0.67 mF·cm −2 at 0.03 mA·cm −2 . The device exhibits strong tissue adhesion with an interfacial toughness of 0.20 kJ·m −2 and a shear strength of 1.5 kPa, resulting from hydrogen bonding, π – π stacking, and electrostatic interactions. A hemolysis rate of 0.35% confirms biocompatibility, while antibacterial properties are provided by the quaternary ammonium salt of chitosan. This work provides a strategy for developing adhesive and biocompatible energy storage components toward future bio ‑ integrated electronics.
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Zhang et al. (2026) studied this question.
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