Abstract
The interaction of a number of nitrogen containing molecules (NO, NH3 and N2H4) with copper has been investigated by electron spectroscopy. Nitric oxide is shown to be molecularly adsorbed in a linearly bonded configuration at 85 K; this adlayer is unstable above 120 K, resulting in an exclusively oxygen adlayer at 295 K, the nitrogen being desorbed. At 85 K N(1s) peaks observed at 401 and 406 eV are associated with NOδ–(ads) and NOδ+(ads) species, the former dissociating and the latter desorbing on thermal activation of the adlayer.Interaction of nitric oxide with Cu at 295 K results in dissociative chemisorption with both oxygen and nitrogen retained at the surface. The surface concentration suggests that each nitrogen and oxygen adatom is bridge-bonded to two surface copper atoms. Estimates of absolute surface coverages are made by comparing the intensities of the N(1s) and O(1s) peaks with the Cu(2p) substrate intensity, while valence level spectroscopy (He I and II radiation) supplements core-level spectroscopy for discriminating between molecular and dissociated surface species.Ammonia dissociates at 295 K on copper while with oxidized copper the surface oxide is replaced by an imide-type surface. With hydrazine, adsorption is molecular over the temperature range 85 to 295 K, in contrast to our observations with iron.
Published Version
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a callMore From: Journal of the Chemical Society, Faraday Transactions 1: Physical Chemistry in Condensed Phases
Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
