Covalently Attached Monolayers on Crystalline Hydrogen-Terminated Silicon:  Extremely Mild Attachment by Visible Light

A very mild method was developed for the attachment of high-quality organic monolayers on crystalline silicon surfaces. By using visible light sources, from 447 to 658 nm, a variety of 1-alkenes and 1-alkynes were attached to hydrogen-terminated Si(100) and Si(111) surfaces at room temperature. The...

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Veröffentlicht in:Journal of the American Chemical Society 2005-03, Vol.127 (8), p.2514-2523
Hauptverfasser: Sun, Qiao-Yu, de Smet, Louis C. P. M, van Lagen, Barend, Giesbers, Marcel, Thüne, Peter C, van Engelenburg, Johan, de Wolf, Frits A, Zuilhof, Han, Sudhölter, Ernst J. R
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Sprache:eng
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Zusammenfassung:A very mild method was developed for the attachment of high-quality organic monolayers on crystalline silicon surfaces. By using visible light sources, from 447 to 658 nm, a variety of 1-alkenes and 1-alkynes were attached to hydrogen-terminated Si(100) and Si(111) surfaces at room temperature. The presence and the quality of the monolayers were evaluated by static water contact angles, X-ray photoelectron spectroscopy, and IR spectroscopy. Monolayers prepared by thermal, UV light, or visible light initiation were compared. Additionally, the ability of infrared reflection−absorption spectroscopy to study organic monolayers on silicon was explored. A reaction mechanism is discussed on the basis of investigations of the reaction behavior of 1-alkenes with silicon wafers with varying types and levels of doping. Finally, a series of mixed monolayers derived from the mixed solutions of a 1-alkene and an ω-fluoro-1-alkene were investigated to reveal that the composition of the mixed monolayers was directly proportional to the molar ratio of the two compounds in the solutions.
ISSN:0002-7863
1520-5126
DOI:10.1021/ja045359s