Scalable Fabrication of Reversible Antifouling Block Copolymer Coatings via Adsorption Strategies

Fouling remains a widespread challenge as its nonspecific and uncontrollable character limits the performance of materials and devices in numerous applications. Although many promising antifouling coatings have been developed to reduce or even prevent this undesirable adhesion process, most of them...

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Veröffentlicht in:ACS applied materials & interfaces 2023-04, Vol.15 (15), p.19682-19694
Hauptverfasser: Maan, Anna M. C., Graafsma, Chantal N., Hofman, Anton H., Pelras, Théophile, de Vos, Wiebe M., Kamperman, Marleen
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Sprache:eng
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Zusammenfassung:Fouling remains a widespread challenge as its nonspecific and uncontrollable character limits the performance of materials and devices in numerous applications. Although many promising antifouling coatings have been developed to reduce or even prevent this undesirable adhesion process, most of them suffer from serious limitations, specifically in scalability. Whereas scalability can be particularly problematic for covalently bound antifouling polymer coatings, replacement by physisorbed systems remains complicated as it often results in less effective, low-density films. In this work, we introduce a two-step adsorption strategy to fabricate high-density block copolymer-based antifouling coatings on hydrophobic surfaces, which exhibit superior properties compared to one-step adsorbed coatings. The obtained hybrid coating manages to effectively suppress the attachment of both lysozyme and bovine serum albumin, which can be explained by its dense and homogeneous surface structure as well as the desired polymer conformation. In addition, the intrinsic reversibility of the adhered complex coacervate core micelles allows for the successful triggered release and regeneration of the hybrid coating, resulting in full recovery of its antifouling properties. The simplicity and reversibility make this a unique and promising antifouling strategy for large-scale underwater applications.
ISSN:1944-8244
1944-8252
DOI:10.1021/acsami.3c01060