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在硅和氢终止的硅衬底上制备的烷基有机单分子层分子聚集态的比较研究。

Comparative study of the molecular aggregation state of alkyl organic monolayers prepared on Si and hydrogen-terminated Si substrates.

作者信息

Ishizaki Takahiro, Saito Nagahiro, Lee Sunhyung, Takai Osamu

机构信息

Department of Materials, Physics and Energy Engineering, Graduate School of Engineering, Nagoya University, Furo-cho, Chikusa, Nagoya 464-8603, Japan.

出版信息

Nanotechnology. 2008 Feb 6;19(5):055601. doi: 10.1088/0957-4484/19/05/055601. Epub 2008 Jan 14.

Abstract

A comparative study of the molecular aggregation states of n-octadecyltrichlorosilane (OTS) and octadecene monolayers was carried out based on water contact angle, x-ray reflectivity (XR), grazing incidence x-ray diffraction (GIXD), and Fourier transform infrared spectroscopy (FT-IR) measurements. Water contact angle, XR, and FT-IR measurements revealed that the packing density and orientational order of the OTS were higher than those of octadecene. The OTS monolayer was in a hexagonal crystalline state with (10) spacing of 0.417 nm, whereas the octadecene monolayer was in an amorphous state. The growth mechanisms of the OTS and octadecene monolayers are also proposed. The alkyl molecular aggregation states strongly depended on the chemical bonding state at the interface between the alkyl organic molecule and the substrate surface.

摘要

基于水接触角、X射线反射率(XR)、掠入射X射线衍射(GIXD)和傅里叶变换红外光谱(FT-IR)测量,对正十八烷基三氯硅烷(OTS)和十八烯单层的分子聚集态进行了比较研究。水接触角、XR和FT-IR测量结果表明,OTS的堆积密度和取向有序度高于十八烯。OTS单层处于六方晶态,(10)间距为0.417 nm,而十八烯单层处于非晶态。还提出了OTS和十八烯单层的生长机制。烷基分子聚集态强烈依赖于烷基有机分子与基底表面之间界面处的化学键合状态。

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