AVS 58th Annual International Symposium and Exhibition | |
Surface Science Division | Wednesday Sessions |
Session SS1-WeM |
Session: | Atomistic Control of Structure & Evolution |
Presenter: | Selena M. Russell, Iowa State University |
Authors: | M. Shen, Iowa State University S.M. Russell, Iowa State University D.-J. Liu, Ames Laboratory - US DOE P.A. Thiel, Iowa State University & Ames Laboratory - US DOE |
Correspondent: | Click to Email |
Studies of chalcogen (O, S) interactions with coinage metal surfaces elucidate how those interactions affect mass transport on the surface and whether a general mechanism exists for these systems. Sulfur accelerates coarsening of Ag nanoislands on Ag(100) at 300 K, and this effect increases with sulfur coverage over a range spanning a few hundredths of a monolayer, to nearly 0.25 monolayers. We propose that acceleration in this system is strongly tied to the formation of AgS2 complexes at step edges. These complexes can transport Ag more efficiently than Ag adatoms (due to a lower diffusion barrier and comparable formation energy), hence leading to enhanced coarsening. The mobility of isolated sulfur on Ag(100) is very low, so that complex formation is kinetically-limited at low sulfur coverages, and thus enhancement is minimal. However, higher sulfur coverages force the population of sites adjacent to step edges, so that formation of the complex is no longer limited by diffusion of sulfur.