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纳米颗粒诱导旋涂聚苯乙烯/聚甲基丙烯酸甲酯共混薄膜的形态调制

Nanoparticle Induced Morphology Modulation in Spin Coated PS/PMMA Blend Thin Films.

作者信息

Das Anuja, Dey Arka Bikash, Chattopadhyay Shreyasi, De Goutam, Sanyal Milan K, Mukherjee Rabibrata

机构信息

Instability and Soft Patterning Laboratory, Department of Chemical Engineering, Indian Institute of Technology Kharagpur, Kharagpur 721302, India.

Saha Institute of Nuclear Physics, Sector 1, AF Block, Bidhan Nagar, Kolkata, West Bengal 700064, India.

出版信息

Langmuir. 2020 Dec 22;36(50):15270-15282. doi: 10.1021/acs.langmuir.0c02584. Epub 2020 Dec 9.

Abstract

The influence of adding nanoparticles on the ascast morphology of spin coated immiscible polystyrene/poly(methyl methacrylate) (PS/PMMA) thin films of different thickness () and composition (, volume ratio of PS to PMMA) has been explored in this article. To understand the precise effect of nanoparticle addition, the morphology of PS/PMMA thin blend films spin cast from toluene on a native oxide covered silicon wafer substrate was first investigated. It is seen that in particle free films, the generic morphology of the films remains nearly unaltered with increase in , for = 3:1 and 1:3. In contrast, strong dependent morphology transformation is observed in films with = 1:1. Subsequently, thiol-capped gold nanoparticles (AuNP) containing films with different particle concentrations () were cast from the same solvent along with the polymer mixture. We observe that addition of AuNPs barely alters the generic morphology of the films with = 3:1. In contrast, the presence of the particles significantly influences the morphology of the films with = 1:1 and 1:3, particularly at higher (≈10.0%). X-ray photoelectron spectroscopy and X-ray reflectivity of some samples reveal that the AuNPs tend to migrate to the free surface through the PS phase, thereby stabilizing this layer partially or fully (depending on ) against dewetting over a surface of adsorbed PMMA layer and influencing the ascast morphology as a function of . The work is fundamentally important in understanding largely overlooked implications of nanoparticle addition on the morphology of PS/PMMA blend thin films which forms the fundamental basis for future interesting studies involving dynamics of nanoparticles within the blend thin films.

摘要

本文探讨了添加纳米颗粒对不同厚度()和组成(,聚苯乙烯与聚甲基丙烯酸甲酯的体积比)的旋涂不相容聚苯乙烯/聚甲基丙烯酸甲酯(PS/PMMA)薄膜铸态形态的影响。为了了解添加纳米颗粒的精确效果,首先研究了从甲苯中旋铸在天然氧化物覆盖的硅片衬底上的PS/PMMA共混薄膜的形态。可以看出,在无颗粒薄膜中,对于 = 3:1和1:3,薄膜的一般形态几乎不会随着的增加而改变。相比之下,在 = 1:1的薄膜中观察到强烈的依赖形态转变。随后,从相同溶剂中与聚合物混合物一起浇铸含有不同颗粒浓度()的硫醇封端金纳米颗粒(AuNP)的薄膜。我们观察到,添加AuNP几乎不会改变 = 3:1的薄膜的一般形态。相比之下,颗粒的存在显著影响 = 1:1和1:3的薄膜的形态,但在更高的(≈10.0%)时尤其如此。一些样品的X射线光电子能谱和X射线反射率表明,AuNP倾向于通过PS相迁移到自由表面,从而部分或完全稳定该层(取决于),防止其在吸附的PMMA层表面上脱湿,并根据影响铸态形态。这项工作对于理解添加纳米颗粒对PS/PMMA共混薄膜形态的影响具有重要意义,而这在很大程度上被忽视了,它构成了未来涉及共混薄膜内纳米颗粒动力学的有趣研究的基础。

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