Please use this identifier to cite or link to this item: https://libjncir.jncasr.ac.in/xmlui/handle/10572/1029
Title: Interaction of Carbon Monoxide with Bimetallic Overlayers
Authors: Santra, A K
Rao, C N R
Keywords: Metal-Metal Bonds
Surfaces
Cu
Chemisorption
Photoemission
Adsorption
Pt(111)
Co
Issue Date: 1994
Publisher: American Chemical Society
Citation: Journal Of Physical Chemistry 98(23), 5962-5965 (1994)
Abstract: Interaction of carbon monoxide with a few chosen bimetallic overlayers has been investigated along with the core-level binding energies of the deposited metals by employing X-rays as well as UV photoelectron spectroscopies. Core-level binding energies of the deposited metals around monolayer coverages (Ѳ∼1) are significantly different than those at high coverages or of the pure metals. Bimetallic overlayers such as Ni/Au and Cu/Pt showing large negative shifts in the surface core-level binding energy of the deposited metal interact strongly with carbon monoxide. In the case of Ni/Au (Ѳ(Ni) similar to 0.85), CO dissociates around 280 K. In contrast to this behavior, the interaction of CO with Pd/Mo or W, showing large positive shifts in the surface core-level binding energy, is very weak, and the CO desorption temperature is much lower than that from the clean Pd metal surface. The CO desorption temperature generally increases as the surface core-level shift of the deposited metal becomes more negative; the separation between the (5σ + 1∏) and 4σ levels of CO also increases in this direction. These results suggest that the variation in the strength of interaction of CO with bimetallic overlayers is a chemical manifestation of the shift in the surface core-level binding energies of the deposited metals at monolayer coverages.
Description: Restricted Access
URI: https://libjncir.jncasr.ac.in/xmlui/10572/1029
Other Identifiers: 0022-3654
Appears in Collections:Research Papers (Prof. C.N.R. Rao)

Files in This Item:
File Description SizeFormat 
sl.no18.1994,J. Phys. Chem. 98, 5962-5965.pdf
  Restricted Access
426.67 kBAdobe PDFView/Open Request a copy


Items in DSpace are protected by copyright, with all rights reserved, unless otherwise indicated.