摘要
Controllable growth of hydrogel coatings on diverse substrates is highly desirable yet remains challenging due to the lack of universal and straightforward fabrication strategies. Herein, we present a visible-light-activated, surface-catalyzed radical polymerization approach that enables the controllable in situ construction of hydrogel coatings on a broad spectrum of materials. The process initiates with the deposition of a P(DMA-co-MEA)@g-C3N4 adhesive primer layer, which not only establishes robust interfacial anchoring to the substrate but also functions as a photocatalytic initiator under visible-light irradiation. This interfacial activation drives spatially confined polymerization, yielding uniform hydrogel coatings with precisely tunable thickness. The method demonstrates extensive substrate compatibility─including metals, polymers, and inorganic materials─and readily affords programmable surface functionalities through interfacial chemical design to impart antifouling, lubricating, or biocompatible properties. Owing to its universality, strong interfacial adhesion, and operational simplicity, this strategy provides a versatile platform for the functional tailoring of irregular and three-dimensional surfaces and holds substantial potential for applications in surface/interface engineering and biorelated technologies.
危险品化学品经营许可证(带存储)