Cardiff University | Prifysgol Caerdydd ORCA
Online Research @ Cardiff 
WelshClear Cookie - decide language by browser settings

The chemisorption and decomposition of pyridine and ammonia at clean and oxidised Al(111) surfaces

Davies, Philip Rosser and Newton, N. G. 2003. The chemisorption and decomposition of pyridine and ammonia at clean and oxidised Al(111) surfaces. Surface Science 546 (2-3) , pp. 149-158. 10.1016/j.susc.2003.09.032

Full text not available from this repository.

Abstract

The nature of the oxygen state at Al(1 1 1) surfaces has been probed by the adsorption of ammonia and pyridine using photoelectron spectroscopy to study reaction products as the sample was warmed from 130 to 540 K. Ammonia only physisorbs at the clean Al(1 1 1) surface but the presence of surface oxygen catalyses a decomposition reaction which leads to the formation of an amide and, on warming to 295 K and above, a nitride. There is no evidence in the XP spectra for the presence of an hydroxyl species or for the desorption of water. Higher oxygen concentrations result in a decrease in the extent of decomposition, with ammonia being stable to 295 K on the pre-oxidised surface. Pyridine partially decomposes at the clean Al(1 1 1) surface at 130 K, giving rise to a well defined intermediate tentatively assigned to an α-pyridyl on the basis of the C:N ratio. Further decomposition occurs on warming with the formation of carbide and nitride by 540 K. Pre-adsorbed oxygen reduces the extent of pyridine decomposition at low temperatures but the species assigned as an α-pyridyl is still formed by room temperature.

Item Type: Article
Date Type: Publication
Status: Published
Schools: Chemistry
Cardiff Catalysis Institute (CCI)
Subjects: Q Science > QD Chemistry
Uncontrolled Keywords: X-ray photoelectron spectroscopy; Chemisorption; Catalysis; Aluminum; Ammonia; Oxygen; Low index single crystal surfaces; Solid–gas interfaces
Publisher: Elsevier
ISSN: 0039-6028
Last Modified: 17 Jun 2017 01:55
URI: http://orca.cf.ac.uk/id/eprint/1416

Citation Data

Cited 8 times in Google Scholar. View in Google Scholar

Cited 15 times in Scopus. View in Scopus. Powered By Scopus® Data

Actions (repository staff only)

Edit Item Edit Item