首页> 外文期刊>Journal of the American Chemical Society >Dehydrative Cyclocondensation Reactions Onrnhydrogen-terminated Si(100) And Si(111): An Ex Situ Tool Forrnthe Modification Of Semiconductor Surfaces
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Dehydrative Cyclocondensation Reactions Onrnhydrogen-terminated Si(100) And Si(111): An Ex Situ Tool Forrnthe Modification Of Semiconductor Surfaces

机译:氢封端的Si(100)和Si(111)的脱水环缩合反应:半导体表面改性的异位工具

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Dehydrative cyclocondensation processes for semiconductor surface modification can be generally suggested on the basis of well-known condensation schemes; however, in practice this approach for organic functionalization of semiconductors has never been investigated. Here we report the modification of hydrogen-terminated silicon surfaces by cyclocondensation. The cyclocondensation reactions of nitrobenzene with hydrogen-terminated Si(100) and Si(111) surfaces are investigated and paralleled with selected cycloaddition reactions of nitro- and nitrosobenzene with Si(100)-2×1. Infrared spectroscopy is used to confirm the reactions and verify an intact phenyl ring and C-N bond in the reaction products as well as the depletion of surface hydrogen. High resolution N 1s X-ray photoelectron spectroscopy (XPS) suggests that the major product for both cyclocondensation reactions investigated is a nitrosobenzene adduct that can only be formed following water elimination. Both IR and XPS are augmented by density functional theory (DFT) calculations that are also used to investigate the feasibility of several surface reaction pathways, which are insightful in understanding the relative distribution of products found experimentally. This novel surface modification approach will be generally applicable for semiconductor functionalization in a highly selective and easily controlled manner.
机译:通常可以基于众所周知的缩合方案提出用于半导体表面改性的脱水环缩合方法。然而,在实践中,从未研究过这种用于半导体的有机功能化的方法。在这里,我们报告通过环缩合对氢封端的硅表面的改性。研究了硝基苯与氢封端的Si(100)和Si(111)表面的环缩合反应,并与选定的硝基和亚硝基苯与Si(100)-2×1的环加成反应平行进行。红外光谱法用于确认反应并验证反应产物中完整的苯环和C-N键以及表面氢的消耗。高分辨率N 1s X射线光电子能谱(XPS)表明,所研究的两个环缩合反应的主要产物都是亚硝基苯加合物,只能在除水后形成。红外和XPS都通过密度泛函理论(DFT)计算得到了增强,该算法还用于研究几种表面反应途径的可行性,这对于理解实验发现的产物的相对分布很有见地。这种新颖的表面改性方法通常将以高度选择性和易于控制的方式适用于半导体功能化。

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