Preparation of dynamic polyurethane networks with UV-triggered photothermal self-healing properties based on hydrogen and ion bonds for antibacterial applications

被引:39
|
作者
Feng, Huimeng [1 ]
Wang, Wei [1 ]
Wang, Tong [1 ]
Zhang, Lei [1 ]
Li, Wen [1 ]
Hou, Jue [1 ]
Chen, Shougang [1 ]
机构
[1] Ocean Univ China, Sch Mat Sci & Engn, Qingdao 266100, Peoples R China
基金
中国国家自然科学基金;
关键词
Cu-dopped ZnO; Ionic bond; Photothermal; Antibacterial; Self-healing; CU-DOPED ZNO; CHARGE-TRANSFER; EFFICIENT; PERFORMANCE; NANOWIRES; EVOLUTION; ABILITY;
D O I
10.1016/j.jmst.2022.06.019
中图分类号
T [工业技术];
学科分类号
08 ;
摘要
Photo-induced self-healing composites have attracted more and more attention as a kind of materials that can be controlled remotely and accurately in real time. Here, we report a strategy of a photo-responsive system based on hydrogen and ion bonds capable of performing self-healing process by ultraviolet wave-lengths, which is covalently cross-linked zinc-dimethylglyoxime-polyurethane coordination network with triple dynamic bonds. The recombination of hydrogen bond and metal coordination bond produces ef-fective healing performance. The self-healing behavior and temperature dependence of 3D micro-crack is investigated by molecular dynamics simulations to reveal the mechanism of self-healing at molecu-lar level. Moreover, the hybrid of copper-doped zinc oxide not only provides metal coordination bonds to enhance the self-healing rate, but also enhances the photothermal effect and anti-bacterial properties of polyurethane. Importantly, doping of copper generates more defects and forms a space charge layer on the surface of zinc oxide. The defects could trap surface electrons and holes, preventing the recom-bination of photo-induced electron-hole pairs, generating more heat through lattice vibration. Therefore, under ultraviolet light irradiation, the polyurethane can reach 62.7 degrees C for 60 s, and the scratches of the polyurethane can be healed within 30 min and fully healed within 1 h. (c) 2022 Published by Elsevier Ltd on behalf of The editorial office of Journal of Materials Science & Technology.
引用
收藏
页码:89 / 101
页数:13
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