In-Plane Movement of Isolated Poly(methacrylate) Chains on a Hydrophilic Solid Surface

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-06-26 DOI:10.1021/acs.macromol.4c00724
Masayuki Kawano, Yuma Morimitsu, Yuwei Liu, Noboru Miyata, Tsukasa Miyazaki, Hiroyuki Aoki, Daisuke Kawaguchi, Satoru Yamamoto, Keiji Tanaka
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Abstract

A better understanding of the dynamic behavior of polymer chains on solid surfaces is indispensable for the design and construction of high-performance polymer composites. We herein visualized the in-plane movement of isolated poly(methyl methacrylate) (PMMA) and poly(tert-butyl methacrylate) (PtBMA) single chains on hydrophilic silicon wafers under ambient conditions by atomic force microscopy. Isolated PMMA chains adsorbed to the substrate, whereas PtBMA chains diffused, the degree of which was dependent on the humidity. Neutron reflectivity revealed the formation of a layer of condensed water on the substrate. All-atomistic molecular dynamics simulations implied that the diffusivity difference of the two polymers was based on the submerged depth in which a part of a chain existed. That is, the interaction of a polymer with the surface of the hydrophilic substrate primarily governs its lateral movement, or adsorption behavior, facilitated by the presence of water.

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亲水性固体表面上分离的聚甲基丙烯酸酯链的平面内运动
要设计和制造高性能聚合物复合材料,就必须更好地了解聚合物链在固体表面上的动态行为。在此,我们通过原子力显微镜观察了孤立的聚甲基丙烯酸甲酯(PMMA)和聚甲基丙烯酸叔丁酯(PtBMA)单链在环境条件下亲水性硅晶片上的平面内运动。分离的 PMMA 链吸附在基底上,而 PtBMA 链则扩散,扩散程度取决于湿度。中子反射率显示基底上形成了一层凝结水。全原子分子动力学模拟表明,两种聚合物的扩散性差异取决于链的一部分存在的浸没深度。也就是说,聚合物与亲水性基底表面的相互作用主要决定了其横向移动或吸附行为,而水的存在则为其提供了便利。
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来源期刊
Macromolecules
Macromolecules 工程技术-高分子科学
CiteScore
9.30
自引率
16.40%
发文量
942
审稿时长
2 months
期刊介绍: Macromolecules publishes original, fundamental, and impactful research on all aspects of polymer science. Topics of interest include synthesis (e.g., controlled polymerizations, polymerization catalysis, post polymerization modification, new monomer structures and polymer architectures, and polymerization mechanisms/kinetics analysis); phase behavior, thermodynamics, dynamic, and ordering/disordering phenomena (e.g., self-assembly, gelation, crystallization, solution/melt/solid-state characteristics); structure and properties (e.g., mechanical and rheological properties, surface/interfacial characteristics, electronic and transport properties); new state of the art characterization (e.g., spectroscopy, scattering, microscopy, rheology), simulation (e.g., Monte Carlo, molecular dynamics, multi-scale/coarse-grained modeling), and theoretical methods. Renewable/sustainable polymers, polymer networks, responsive polymers, electro-, magneto- and opto-active macromolecules, inorganic polymers, charge-transporting polymers (ion-containing, semiconducting, and conducting), nanostructured polymers, and polymer composites are also of interest. Typical papers published in Macromolecules showcase important and innovative concepts, experimental methods/observations, and theoretical/computational approaches that demonstrate a fundamental advance in the understanding of polymers.
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