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硅上有机线条形成的场导向和自模板效应的指示。

Indications of field-directing and self-templating effects on the formation of organic lines on silicon.

机构信息

Department of Physics, University of Alberta, Edmonton, Alberta, Canada T6G 2G7.

出版信息

J Chem Phys. 2011 Mar 21;134(11):114707. doi: 10.1063/1.3562367.

Abstract

It has previously been shown that multimolecular organic nanostructures form on H-Si(100)-2×1 via a radical mediated growth process. In this mechanism, growth begins through the addition of a molecule to a silicon surface dangling bond, followed by the abstraction of a neighboring H atom and generation of a new dangling bond on the neighboring site. Nanostructures formed by this mechanism grow along one edge of a dimer row. Here, we explored the possibility of using lithographically prepared, biased metal contacts on the silicon surface to generate an electric field that orients molecules during the growth process to achieve growth in the perpendicular-to-row direction. The formation of some nanostructures in a direction that was nearly perpendicular to the dimer rows was achieved, whereas such features were not formed in the absence of the field. Analysis of the scanning tunneling microscopy images suggests that the formation of these nanostructures may involve self-templating effects in addition to dangling bond diffusion rather than a straightforward addition∕abstraction mechanism. These initial results offer some indication that a molecular pattern writer can be achieved.

摘要

先前已经表明,多分子有机纳米结构通过自由基介导的生长过程在 H-Si(100)-2×1 上形成。在这个机制中,生长通过将一个分子添加到硅表面的悬空键开始,随后是相邻 H 原子的提取和相邻位置上新悬空键的生成。通过这个机制形成的纳米结构沿着二聚体行的一个边缘生长。在这里,我们探索了使用硅表面上光刻制备的偏置金属接触来产生电场的可能性,该电场在生长过程中定向分子以实现沿行垂直方向的生长。在没有电场的情况下,实现了一些几乎垂直于二聚体行的方向上的纳米结构的形成,而在没有电场的情况下则没有形成这样的特征。扫描隧道显微镜图像的分析表明,这些纳米结构的形成可能涉及悬空键扩散之外的自模板效应,而不是直接的加成∕消去机制。这些初步结果表明可以实现分子图案写入器。

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