Covalently attached monolayers on crystalline hydrogen-terminated silicon: Extremely mild attachment by visible light

Q. Sun, L.C.P.M. Smet, de, B. Lagen, van, M. Giesbers, P.C. Thune, J. Engelenburg, van, F. Wolf, de, H. Zuilhof, E.J.R. Sudhoelter

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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(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 ¿-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.
Original languageEnglish
Pages (from-to)2514-2523
Number of pages9
JournalJournal of the American Chemical Society
Volume127
Issue number8
DOIs
Publication statusPublished - 2005

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