多功能贻贝启发的水凝胶和膜形成的儿茶酚-二氧化氧纳米粒子配位。

IF 4.3 3区 化学 Q2 POLYMER SCIENCE
Mostafa Rammal, Matthew J Harrington
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引用次数: 0

摘要

海洋贻贝利用DOPA-V金属配位键作为动态交联来制造坚韧和自我修复的涂层和胶水。受贻贝的启发,研究人员利用多巴-金属配位来创造动态和机械响应的聚合物材料。在这里,我们利用在贻贝中观察到的强大的DOPA-V相互作用,结合二氧化钒(VO2)的温度响应特性,开发了一种室温工艺来生产热致变色的VO2水凝胶和薄膜。用dopa -儿茶酚基团功能化的四臂聚乙二醇(PEG)聚合物与VO2纳米颗粒在溶液中混合。提高pH值导致水凝胶的形成,而旋转涂层使加工成薄膜成为可能。水凝胶具有机械可调的粘弹性和自愈反应。此外,干燥后的独立薄膜具有高度的柔韧性,并表现出200%以上的塑性变形,同时仍保留了纳米颗粒的热致变色特性。简便的制造方法和由此产生的多功能机械响应与热致变色性能相结合,是未来发展vo2聚合物复合材料的前景。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multifunctional Mussel-Inspired Hydrogels and Films Formed via Catechol-VO2 Nanoparticle Coordination.

Marine mussels utilize DOPA-V metal coordination bonds as dynamic cross-links to fabricate tough and self-healing coatings and glues. Inspired by mussels, researchers have harnessed DOPA-metal coordination to create dynamic and mechanically responsive polymeric materials. Here, we harness the robust DOPA-V interactions observed in mussels combined with the temperature-responsive properties of vanadium dioxide (VO2) to develop a room-temperature process to produce thermochromic VO2 hydrogels and films. 4-arm polyethylene glycol (PEG) polymers functionalized with DOPA-catechol moieties were mixed with VO2 nanoparticles in solution. Raising pH led to formation of hydrogels, while spin coating enabled processing into thin films. Hydrogels possessed mechanically tunable viscoelasticity and self-healing response. Furthermore, dried free-standing films were highly flexible and exhibited plastic deformation with extensibilities of 200% and beyond, while still retaining the thermochromic properties of the nanoparticles. The facile fabrication method and the resulting versatile mechanical response combined with thermochromic properties are promising for future development VO2-polymer composite materials.

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来源期刊
Macromolecular Rapid Communications
Macromolecular Rapid Communications 工程技术-高分子科学
CiteScore
7.70
自引率
6.50%
发文量
477
审稿时长
1.4 months
期刊介绍: Macromolecular Rapid Communications publishes original research in polymer science, ranging from chemistry and physics of polymers to polymers in materials science and life sciences.
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