The adsorption of nitromethane (CH3NO2 and CD3NO2) and d3-methyl nitrite (CD3ONO) on Au(111) was studied by temperature-programmed desorption (TPD) and high-resolution electron energy loss spectroscopy (HREELS). These molecules are only weakly adsorbed on Au(111), and adsorption is completely reversible in both cases. Adsorbed CH3NO2 and CD3ONO in the monolayer each give rise to one thermal desorption peak in TPD with desorption activation energies of 10.5 and 8 kcal/mol, respectively. These desorption energies are close to the values for the heats of adsorption of these molecules, since there is no appreciable activation energy for molecular adsorption. HREELS confirms weak, molecular adsorption in the monolayer for both molecules. Furthermore, nitromethane is bonded on Au(111) in an upright, strongly tilted geometry, suggesting a monodentate coordination to the surface. Methyl nitrite adsorbs on Au(111) with the O-N=O group in a flat-King geometry, with evidence for both cis and trans forms. The Au(111) surface does not sufficiently activate nitromethane and methyl nitrite for dissociation or isomerization (CH3NO2 ↔ CH3ONO) to occur under UHV conditions. Thus the activation energies for dissociation and isomerization of nitromethane on Au(111) exceed 10.5 kcal/mol.
|Original language||English (US)|
|Number of pages||9|
|State||Published - Jun 9 1998|
All Science Journal Classification (ASJC) codes
- Materials Science(all)
- Condensed Matter Physics
- Surfaces and Interfaces