Engineering Active-Site-Induced Homogeneous Growth of Polydopamine Nanocontainers on Loading-Enhanced Ultrathin Graphene for Smart Self-Healing Anticorrosion Coatings

材料科学 石墨烯 自愈 涂层 纳米技术 钝化 同种类的 腐蚀 剥脱关节 复合材料 图层(电子) 医学 热力学 物理 病理 替代医学
作者
Guangyan Chen,Bao Jin,Zhehao Zhang,Jun Zhao,Yunze Li,Yongyong He,Jianbin Luo
出处
期刊:ACS Applied Materials & Interfaces [American Chemical Society]
卷期号:15 (19): 23679-23689 被引量:36
标识
DOI:10.1021/acsami.3c03276
摘要

Engineering nanocontainers with encapsulated inhibitors onto graphene has been an emerging technology for developing self-healing anticorrosion coatings. However, the loading contents of inhibitors are commonly limited by inhomogeneous nanostructures of graphene platforms. Here, we propose an activation-induced ultrathin graphene platform (UG-BP) with the homogeneous growth of polydopamine (PDA) nanocontainers encapsulated with benzotriazole (BTA). Ultrathin graphene prepared by catalytic exfoliation and etching activation provides an ideal platform with an ultrahigh specific surface area (1646.8 m2/g) and homogeneous active sites for the growth of PDA nanocontainers, which achieves a high loading content of inhibitors (40 wt %). The obtained UG-BP platform exhibits pH-sensitive corrosion inhibition effects due to its charged groups. The epoxy/UG-BP coating possesses integrated properties of enhanced mechanical properties (>94%), efficient pH-sensitive self-healing behaviors (98.5% healing efficiency over 7 days), and excellent anticorrosion performance (4.21 × 109 Ω·cm2 over 60 days), which stands out from previous related works. Moreover, the interfacial anticorrosion mechanism of UG-BP is revealed in detail, which can inhibit the oxidation of Fe2+ and promote the passivation of corrosion products by a dehydration process. This work provides a universal activation-induced strategy for developing loading-enhanced and tailor-made graphene platforms in extended smart systems and demonstrates a promising smart self-healing coating for advanced anticorrosion applications.
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