Self-assembly of octadecyltrichlorosilane monolayers on silicon-based substrates by chemical vapor deposition

十八烷基三氯氢硅 单层 接触角 化学气相沉积 材料科学 自组装单层膜 纳米技术 化学工程 硅烷 基质(水族馆) X射线光电子能谱 化学 分析化学(期刊) 光电子学 有机化学 复合材料 工程类 海洋学 地质学
作者
Jinsheng Dong,Anfeng Wang,K. Y. Simon Ng,Guangzhao Mao
出处
期刊:Thin Solid Films [Elsevier]
卷期号:515 (4): 2116-2122 被引量:91
标识
DOI:10.1016/j.tsf.2006.07.041
摘要

Increasingly, organosilane self-assembled monolayers (SAMs) are used to modify the surfaces of silicon-based sensors and atomic force microscope (AFM) probes. Organosilane SAMs are preferred due to their fast and easy preparation, stability, and applicability to a wide range of substrates. The traditional dip coating method from solution often yields ill-defined particulate aggregates on the two-dimensional SAM. The presence of such three-dimensional aggregates seriously reduces the performance of miniaturized biosensor devices and AFM probes. It is difficult to control the amount of water in solution-based deposition. This paper describes a chemical vapor deposition (CVD) method to deposit octadecyltrichlorosilane (OTS) monolayers on silicon wafers and AFM probes under vacuum condition. OTS coated surfaces with static water contact angle ranging from 20° to 107° can be obtained by controlling the deposition conditions. The silicon substrates and AFM probes after CVD are characterized by AFM, X-ray photoelectron spectroscopy, Fourier transform infrared spectroscopy, and contact angle goniometry. The OTS monolayer is in a uniform low-density state below 65%. Above 65%, densely packed crystalline-like domains start to form. It takes 24 h to reach the adsorption saturation. The time span in the CVD deposition is much longer than the solution case and thus allowing precise variation of the substrate hydrophobicity for biosensor applications.

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