Reactivity of CO on stepped and non-stepped surfaces of transition metals

Abstract

Results of extended Huckel calculations show that coordination of CO to Group VIII transition-metal surfaces depends on a subtle balance of the interaction with the CO 5σ orbital, that tends to direct the CO molecule to the atop position and the CO 2 π* orbital, that directs the molecule to higher coordination sites. In the atop position, the changes in bonding to different surfaces of the same metal can be mainly attributed to differences in the interaction with the CO 5σ molecular orbital. The favoured dissociation path is such that carbon and oxygen atoms end in high coordination sites, sharing as few surface metal atoms as possible. The CO bond is activated by the metal atoms that are crossed upon dissociation.