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Sulfur-induced mobilization of Au surface atoms on Au(1 1 1) studied by real-time STM
Authors:Monika M Biener  Juergen Biener  Cynthia M Friend
Institution:a Department of Chemistry, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA
b Division of Engineering and Applied Sciences, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA
c Center for Imaging and Mesoscale Structures, Harvard University, 12 Oxford Street, Cambridge, MA 02138, USA
d Nanoscale Synthesis and Characterization Laboratory, Lawrence Livermore National Laboratory, 7000 East Ave, Livermore, CA 94550, USA
Abstract:The interaction of sulfur with gold surfaces has attracted considerable interest due to numerous technological applications such as the formation of self-assembled monolayers and as a chemical sensor. Here, we report on the interaction of sulfur with Au(1 1 1) at two different temperatures (300 K and 420 K) studied by real-time scanning tunnelling microscopy, low energy electron diffraction and Auger electron spectroscopy. In the low coverage regime (<0.1 ML), S adsorption lifts the herringbone reconstruction of the clean Au(1 1 1) surface indicating a lateral expansion of the surface layer. An ordered (√3 × √3)R30° sulfur adlayer develops as the coverage reaches ∼0.3 ML. At higher S coverages (>0.3 ML) gold surface atoms are removed from regular terrace sites and incorporated into a growing gold sulfide phase. At 300 K this process leads to the formation of a rough pit and mound surface morphology. This gold sulfide exhibits short-range order and an incommensurate, long-range ordered AuS phase develops upon annealing at 450-525 K. In contrast, formation of an ordered AuS phase via rapid step-retraction rather than etch pit formation is observed during S-interaction with Au(1 1 1) surfaces at 420 K. Our results shed new light on the S-Au(1 1 1) interaction.
Keywords:Scanning tunnelling microscopy  Low energy electron diffraction  Auger electron spectroscopy  Corrosion  Surface chemical reaction  Gold  Sulfur
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