THE EFFECTS OF PREADSORBED CO ON THE CHEMISTRY OF CH3 AND CH3I ON PD(111)

The thermal decomposition of iodomethane on clean, I-precovered and CO -precovered Pd{111} is investigated using thermal desorption spectrosc opy (TDS) and X-ray photoelectron spectroscopy (XPS). On a clean surfa ce, CH3I decomposes to produce CH3,ads and I(ads) at temperatures betw een 175 and 200 K. No evidence of C2-hydrocarbon formation is observed . The CH3,ads produced by C-I bond activation hydrogenates to desorb a s CH4 at 200 K. The I(ads) remains on the surface below 850 K and comp letely desorbs by 1100 K. The I(ads) behaves as a site blocker which r emoves activation sites for C-I bond activation without changing the c hemical activity of CH3,ads. Compared with the results obtained from o ther laboratories, the thermal decomposition of CH3I on Pd is a strong structure-sensitive reaction. It was found that the C-I bond breaks a t a temperature as low as 95 K on Pd{100}, whereas the C-I bond cleava ge can only be observed at temperatures above 175 K on Pd{111}. The pr esence of CO on Pd{111} inhibits the C-I bond breaking which simultane ously influences the thermal stability of CH3,ads. Depending upon the initial coverage of CO, the hydrogenation of CH3,ads to CH4 occurs at temperatures which are up to 80 K higher than for the clean surface. T he enhancement of the thermal stability of CH3,ads may result from bot h site blocking and electronic effects induced by preadsorbed CO.