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铜硫化物锚定 MXene 提高光响应自修复聚氨酯的力学和抗菌性能。

Copper sulfide anchored MXene improving photo-responsive self-healing polyurethane with enhanced mechanical and antibacterial properties.

机构信息

School of Materials Science and Engineering, Ocean University of China, Qingdao 266100, China.

School of Materials Science and Engineering, Ocean University of China, Qingdao 266100, China.

出版信息

J Colloid Interface Sci. 2023 Jan 15;630(Pt B):511-522. doi: 10.1016/j.jcis.2022.10.089. Epub 2022 Oct 26.

Abstract

Diseases caused by bacterial infection are becoming a major threat to human health. Therefore, developing efficient antibacterial materials is of great significance in improving medical care and protecting people's health. In this work, an accordion-like structural TiC@CuS was synthesized by copper sulfide (CuS) nanospheres anchored firmly on the surface of TiCT via the hydrothermal method. The multilayer TiC@CuS becomes few-layered nanosheets after ultrasonic treatment, which have an enjoyable dispersion in the polyurethane (PU) matrix. PU and the released Cu from TiC@CuS are firmly linked by a coordination bond, which improves the mechanical properties and thermal stability of TiC@CuS-PU and reduces the heavy metal ion pollution by blocking the Cu released by forming coordination bonds. Moreover, TiC@CuS-PU exhibits an excellent self-healing performance after 30 tensile cycles. Additionally, TiCT and CuS could improve the separation efficiency of the electron-hole pairs of CuS to produce more reactive oxygen species (ROS) to kill bacteria. TiC@CuS-PU maintains a highly long-term sterilization ability of more than 90 % in 30 days because of the synergistic effect of the sustained release of copper ions, the elevated ROS production ability, and the excellent dispersion of TiC@CuS in PU. This work demonstrates a simple and promising route for designing multifunctional antibacterial self-healing materials.

摘要

由细菌感染引起的疾病正成为人类健康的主要威胁。因此,开发高效的抗菌材料对于改善医疗保健和保护人们的健康具有重要意义。在这项工作中,通过水热法将硫化铜(CuS)纳米球牢固地锚定在 TiCT 表面上,合成了一种类似手风琴结构的 TiC@CuS。经过超声处理后,多层 TiC@CuS 变成了少层纳米片,在聚氨酯(PU)基体中具有良好的分散性。PU 和 TiC@CuS 释放的 Cu 通过配位键牢固结合,提高了 TiC@CuS-PU 的力学性能和热稳定性,并通过形成配位键来阻止 Cu 的释放,减少重金属离子污染。此外,TiC@CuS-PU 在 30 次拉伸循环后表现出优异的自修复性能。此外,TiCT 和 CuS 可以提高 CuS 中电子-空穴对的分离效率,产生更多的活性氧(ROS)来杀死细菌。由于铜离子的持续释放、ROS 产生能力的提高以及 TiC@CuS 在 PU 中的优异分散性的协同作用,TiC@CuS-PU 在 30 天内保持了超过 90%的长期杀菌能力。这项工作展示了一种设计多功能抗菌自修复材料的简单而有前途的途径。

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