Covalent Attachment of Acetylene and Methylacetylene Functionality to Si(111) Surfaces: Scaffolds for Organic Surface Functionalization while Retaining Si−C Passivation of Si(111) Surface Sites

Abstract

Si(111) surfaces have been functionalized with Si−C⋮C−R species, where R = H or –CH_3, using a two-step reaction sequence involving chlorination of H−Si(111) followed by treatment with Na−C⋮C−H or CH_3−C⋮C−Na reagents. The resulting surfaces showed no detectable oxidation as evidenced by X-ray photoelectron spectroscopic (XPS) data in the Si 2p region, electrochemical measurements of Si−H oxidation, or infrared spectroscopy. The Si−C⋮C−R-terminated surfaces exhibited a characteristic C⋮C stretch in the infrared at 2179 cm^(-1), which was strongly polarized perpendicular to the Si(111) surface plane. XPS measurements in the C 1s region showed a low binding energy peak indicative of Si−C bonding, with a coverage that was, within experimental error, identical to that of the CH_3-terminated Si(111) surface, which has been shown to fully terminate the Si atop sites on an unreconstructed Si(111) surface. The Si−C⋮C−H-terminated surfaces were further functionalized by exposure to n-C_4H_9Li followed by exposure to para Br−C_6H_5−CF_3, allowing for introduction of para –C_6H_5CF_3 groups while maintaining the desirable chemical and electrical properties that accompany complete Si−C termination of the atop sites on the Si(111) surface.

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