Film Thickness Dependence of Surface and Internal Morphology Evolution in Polymer-Grafted Nanocomposites

IF 5.1 1区 化学 Q1 POLYMER SCIENCE Macromolecules Pub Date : 2024-06-28 DOI:10.1021/acs.macromol.4c00854
Aria C. Zhang, Kohji Ohno, Russell J. Composto
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Abstract

This study investigates the interplay between film thickness and the surface and internal morphologies in polymer nanocomposite (PNC) films. The PNC is 25 wt % poly(methyl methacrylate)-grafted silica nanoparticles (NPs) in poly(styrene-ran-acrylonitrile) annealed in the two-phase region. At greatest confinement (120 nm), NP surface density remains constant, and lateral phase separation is inhibited upon annealing. For thicker films (240–1400 nm), surface density increases with time before approaching ca. 740 NP/μm2, consistent with 2D random close packing. Moreover, lateral domain growth exhibits a dimensional crossover as thickness increases from t1/2 to t1/3, consistent with domain coalescence. Water contact angles decrease upon annealing in agreement with the lateral domain composition. For thickest films (1400–4000 nm), a morphology map summarizes the distinct internal arrangements of NPs: disordered aggregates, continuous vertical pillars, discrete vertical pillars, isolated domains, and random networks. This study of PNC films provides guidance for controlling surface and bulk structure which can lead to improved barrier, mechanical, and transport properties.

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聚合物接枝纳米复合材料表面和内部形态演变的膜厚依赖性
本研究探讨了聚合物纳米复合材料(PNC)薄膜厚度与表面和内部形态之间的相互作用。PNC 是 25 wt % 聚(甲基丙烯酸甲酯)接枝二氧化硅纳米粒子(NPs)在两相区退火的聚(苯乙烯-然丙烯腈)。在最大限制条件下(120 nm),NP 表面密度保持不变,退火时横向相分离受到抑制。对于较厚的薄膜(240-1400 nm),表面密度会随着时间的推移而增加,然后接近约 740 NP/μm2,这与二维无规紧密堆积一致。此外,随着厚度从 t1/2 增加到 t1/3,横向畴生长出现了尺寸交叉,这与畴凝聚一致。退火后,水接触角减小,这与横向畴的组成一致。对于最厚的薄膜(1400-4000 nm),形态图概括了 NPs 不同的内部排列:无序聚集体、连续垂直柱、离散垂直柱、孤立畴和随机网络。这项对 PNC 薄膜的研究为控制表面和块体结构提供了指导,从而提高了阻隔、机械和传输性能。
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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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