Vegunta Sri Sai S, Ngunjiri Johnpeter N, Flake John C
Gordon and Mary Cain Department of Chemical Engineering, Louisiana State University, Baton Rouge, Louisiana 70803, USA.
Langmuir. 2009 Nov 3;25(21):12750-6. doi: 10.1021/la9018103.
Passivation of (100) silicon surfaces using alkyl Grignard reagents is explored via electrochemical and thermal grafting methods. The electrochemical behavior of silicon in methyl or ethyl Grignard reagents in tetrahydrofuran is investigated using cyclic voltammetry. Surface morphology and chemistry are investigated using atomic force microscopy, Fourier transform infrared spectroscopy, and X-ray photoelectron spectroscopy (XPS). Results show that electrochemical pathways provide an efficient and more uniform passivation method relative to thermal methods, and XPS results demonstrate that electrografted terminations are effective at limiting native oxide formation for more than 55 days in ambient conditions. A two-electron per silicon mechanism is proposed for electrografting a single (1:1) alkyl group per (100) silicon atom. The mechanism includes oxidation of two Grignard species and subsequent hydrogen abstraction and alkylation reaction resulting in a covalent attachment of alkyl groups with silicon.
通过电化学和热接枝方法探索了使用烷基格氏试剂对(100)硅表面进行钝化。采用循环伏安法研究了硅在甲基或乙基格氏试剂的四氢呋喃溶液中的电化学行为。使用原子力显微镜、傅里叶变换红外光谱和X射线光电子能谱(XPS)研究了表面形貌和化学性质。结果表明,相对于热方法,电化学途径提供了一种高效且更均匀的钝化方法,XPS结果表明,在环境条件下,电接枝的端基在超过55天的时间内有效地限制了原生氧化物的形成。提出了一种每硅两个电子的机制,用于在每个(100)硅原子上电接枝单个(1:1)烷基。该机制包括两个格氏试剂物种的氧化,随后的氢原子提取和烷基化反应,导致烷基与硅的共价连接。