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Fluorescence correlation spectroscopy in thin films at reflecting substrates as a means to study nanoscale structure and dynamics at soft-matter interfaces

机译:反射基材上薄膜的荧光相关光谱法,作为研究软物质界面上纳米级结构和动力学的一种手段

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摘要

Structure and dynamics at soft-matter interfaces play an important role in nature and technical applications. Optical single-molecule investigations are noninvasive and capable to reveal heterogeneities at the nanoscale. In this work we develop an autocorrelation function (ACF) approach to retrieve tracer diffusion parameters obtained from fluorescence correlation spectroscopy (FCS) experiments in thin liquid films at reflecting substrates. This approach then is used to investigate structure and dynamics in 100-nm-thick 8CB liquid crystal films on silicon wafers with five different oxide thicknesses. We find a different extension of the structural reorientation of 8CB at the solid-liquid interface for thin and for thick oxide. For the thin oxides, the perylenediimide tracer diffusion dynamics in general agrees with the hydrodynamic modeling using no-slip boundary conditions with only a small deviation close to the substrate, while a considerably stronger decrease of the interfacial tracer diffusion is found for the thick oxides.
机译:软物质接口的结构和动力学在自然和技术应用中起着重要作用。光学单分子研究是非侵入性的,能够揭示纳米级的异质性。在这项工作中,我们开发了一种自相关函数(ACF)方法,以检索从荧光相关光谱(FCS)实验在反射基板上的薄膜中获得的示踪剂扩散参数。然后,该方法用于研究具有五种不同氧化物厚度的硅晶片上100纳米厚的8CB液晶膜的结构和动力学。我们发现,对于薄氧化物和厚氧化物,固-液界面处8CB的结构重新取向都有不同的扩展。对于薄氧化物,the二酰亚胺示踪剂扩散动力学通常与使用无滑移边界条件的流体力学模型一致,仅在靠近基底的地方有很小的偏差,而厚氧化物则发现界面示踪剂扩散的明显更强的降低。

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