Multifunctional antifogging, self-cleaning, antibacterial, and self-healing coatings based on polyelectrolyte complexes

被引:20
作者
Kong, Ruixia [1 ]
Ren, Jingli [1 ]
Mo, Min [1 ]
Zhang, Lianbin [1 ]
Zhu, Jintao [1 ]
机构
[1] Huazhong Univ Sci & Technol HUST, Hubei Engn Res Ctr Biomat & Med Protect Mat, Sch Chem & Chem Engn, Wuhan 430074, Peoples R China
基金
中国国家自然科学基金;
关键词
Antifogging coating; Self-cleaning; Antibacterial; Self-healing; Polyelectrolyte complexes; UNDERWATER SUPEROLEOPHOBICITY; HIGHLY TRANSPARENT; COMPOSITE FILMS; TANNIC-ACID; ANTI-FOG; SURFACE; DESIGN; ROBUST; POLYETHYLENIMINE; FABRICATION;
D O I
10.1016/j.colsurfa.2022.130484
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
In this study, a multifunctional coating with antifogging, self-cleaning, antibacterial, and self-healing capabilities is developed based on polyelectrolyte complexes of polyethylenimine (PEI), phytic acid (PA), and Cu2+ (denoted as PEI-PA-Cu). The multifunctional PEI-PA-Cu coating with high transparency can be prepared by spraying, brushing, or other one-step deposition onto various substrates (e.g., polymeric substrates and glass slides). Such a coating shows an excellent antifogging effect in both high temperature (85 degrees C) and cold environments (-20 degrees C) and maintains stable antifogging performance after placing in similar to 65 degrees C vapor for 9 h. In addition, the coating is superhydmphilic and allows for easy spreading of water to isolate the oily contaminants, realizing self-cleaning. Meanwhile, the coating possesses superior antibacterial capability against Escherichia coli and Staphylococcus aureus thanks to PEI with amino groups and Cu2+. Importantly, the PEI-PA-Cu coating can heal damages rapidly and repeatedly due to the presence of hydrogen bonds and electrostatic interactions, effectively prolonging the service life. This study provides a facile route to construct multifunctional superhydrophilic coatings with promising prospects in the field of personal protective, medical, and optical devices.
引用
收藏
页数:10
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