Abstract
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(IOO) 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. © 2005 American Chemical Society.
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CITATION STYLE
Sun, Q. Y., De Smet, L. C. P. M., Van Lagen, B., Giesbers, M., Thüne, P. C., Van Engelenburg, J., … Sudhölter, E. J. R. (2005). Covalently attached monolayers on crystalline hydrogen-terminated silicon: Extremely mild attachment by visible light. Journal of the American Chemical Society, 127(8), 2514–2523. https://doi.org/10.1021/ja045359s
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