Abstract
We deposited Os atoms on S- and Se-doped boronic graphenic surfaces by electron bombardment of micelles containing 16e complexes [Os(p-cymene)(1,2-dicarba-closo-dodecarborane-1,2-diselenate/dithiolate)] encapsulated in a triblock copolymer. The surfaces were characterized by energy-dispersive X-ray (EDX) analysis and electron energy loss spectroscopy of energy filtered TEM (EFTEM). Os atoms moved ca. 26× faster on the B/Se surface compared to the B/S surface (233 ± 34 pm·s-1 versus 8.9 ± 1.9 pm·s-1). Os atoms formed dimers with an average Os-Os distance of 0.284 ± 0.077 nm on the B/Se surface and 0.243 ± 0.059 nm on B/S, close to that in metallic Os. The Os2 molecules moved 0.83× and 0.65× more slowly than single Os atoms on B/S and B/Se surfaces, respectively, and again markedly faster (ca. 20×) on the B/Se surface (151 ± 45 pm·s-1 versus 7.4 ± 2.8 pm·s-1). Os atom motion did not follow Brownian motion and appears to involve anchoring sites, probably S and Se atoms. The ability to control the atomic motion of metal atoms and molecules on surfaces has potential for exploitation in nanodevices of the future.
Original language | English |
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Pages (from-to) | 5100-5105 |
Number of pages | 6 |
Journal | Chemistry of Materials |
Volume | 27 |
Issue number | 14 |
Early online date | 6 Jul 2015 |
DOIs | |
Publication status | Published - 28 Jul 2015 |
ASJC Scopus subject areas
- General Chemistry
- General Chemical Engineering
- Materials Chemistry