Effect of Thermal Annealing on the Bound Layer in Polymer Thin Films: Insights from Swelling Kinetics and Guiselin’s Approach

IF 5.2 1区 化学 Q1 POLYMER SCIENCE
Sonam Zangpo Bhutia, Sivasurender Chandran, Sathish K. Sukumaran, Dillip K. Satapathy
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Abstract

In supported polymer thin films, dependent on the polymer–substrate interactions, a distinct polymer layer forms next to the polymer–substrate interface. This distinct, buried layer is typically investigated using “Guiselin’s approach” which involves washing the thin film in a good solvent. Recently, we introduced a novel approach wherein the thickness of the distinct layer was obtained using only the swelling kinetics of the thin films. However, the relationship between the characteristics of the distinct layer as determined by the two approaches remains unclear. To address this, we have used spectroscopic ellipsometry and X-ray reflectivity measurements of spin-coated PVA thin films to systematically compare the characteristics of the “bound layer”, determined using an analysis of the time-dependent swelling, and the “adsorbed layer”, obtained using Guiselin’s approach. In particular, we investigated the effect of annealing above Tg for varying time durations, tann. The thickness of the bound layer, ds, and that of the adsorbed layer, dads, were found to be nearly independent of the initial (dry) thickness of the thin film, d(0). For tann = 0, ds ≈ 5 dads, suggesting that the bound layer included a significant fraction of chains that were weakly adsorbed. With increasing tann, ds exhibited a monotonic decrease from ≈15 nm to a plateau value of ≈7 nm, while dads exhibited a rapid monotonic increase from ≈3 nm and approached a plateau value of ≈11 nm. Irrespective of tann and dads(0), the adsorbed layers exhibited a maximum increase in thickness of ≈2.7–4.5 nm when exposed to H2O vapor. Interestingly, upon increasing tann, while the short-time diffusion coefficient of H2O into the polymer thin film was found to decrease by approximately an order of magnitude, the corresponding effect on the adsorbed layer appeared to be significantly weaker.

Abstract Image

热退火对聚合物薄膜结合层的影响:来自膨胀动力学和Guiselin方法的见解
在支撑聚合物薄膜中,根据聚合物与基底的相互作用,聚合物与基底界面旁边会形成一个独特的聚合物层。通常采用 "Guiselin 方法 "来研究这种独特的埋藏层,即用良好的溶剂清洗薄膜。最近,我们引入了一种新方法,即仅利用薄膜的溶胀动力学来获得独立层的厚度。然而,这两种方法所确定的独立层特征之间的关系仍不清楚。为了解决这个问题,我们使用旋涂 PVA 薄膜的光谱椭偏仪和 X 射线反射率测量法,系统地比较了使用随时间变化的溶胀分析法确定的 "结合层 "和使用 Guiselin 方法获得的 "吸附层 "的特征。我们特别研究了在不同的时间长度(tann)下,在 Tg 以上退火的影响。研究发现,结合层的厚度 ds 和吸附层的厚度 dads 几乎与薄膜的初始(干)厚度 d(0) 无关。当 tann = 0 时,ds ≈ 5 dads,这表明结合层包含了相当一部分弱吸附的链。随着鞣质的增加,ds 从≈15 nm 单调下降到≈7 nm 的高位值,而 dads 则从≈3 nm 快速单调增加,接近≈11 nm 的高位值。无论鞣质和dads(0)如何变化,当吸附层暴露在H2O蒸气中时,其厚度的最大增幅为≈2.7-4.5 nm。有趣的是,当鞣质增加时,虽然发现 H2O 进入聚合物薄膜的短时间扩散系数降低了约一个数量级,但对吸附层的相应影响似乎要弱得多。
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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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