Molecules on oxide surfaces
Metal oxides may be prepared as thin (5–50 Å) films on top of metallic substrates. By such means oxide substrates with properties identical to bulk oxides may be formed which can be studied via electron spectroscopies without being hindered by charging, as well as cooling problems. We report here on...
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Published in: | Catalysis today Vol. 32; no. 1; pp. 1 - 10 |
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Main Authors: | , , , , , , , |
Format: | Journal Article Conference Proceeding |
Language: | English |
Published: |
Amsterdam
Elsevier B.V
16-12-1996
Elsevier Science |
Subjects: | |
Online Access: | Get full text |
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Summary: | Metal oxides may be prepared as thin (5–50 Å) films on top of metallic substrates. By such means oxide substrates with properties identical to bulk oxides may be formed which can be studied via electron spectroscopies without being hindered by charging, as well as cooling problems. We report here on results on NiO and on Cr
2O
3 surfaces.
We discuss some structural aspects of oxide surfaces such as surface reconstruction of polar rock salt-type surfaces, and structural phase transitions on corundum type structures. The nature of the phase transition will be discussed with respect to the magnetic properties of the oxide.
Furthermore we report on the interaction of those surfaces with molecules from the gas phase. In particular we study the interaction with small molecules such as CO, NO, O
2, CO
2, H
2O and C
2H
4. We observe via various surface sensitive techniques such as thermal desorption spectroscopy (TDS), X-ray photoelectron spectroscopy (XPS), angle resolved photoemission (ARUPS), electron energy loss spectroscopy (HREELS), infrared-reflection-absorption-spectroscopy (IRAS), and near-edge-X-ray-absorption-fine-structure spectroscopy (NEXAFS), associative as well as dissociative adsorption and in the case of ethylene also polymerization reactions. Via isotopic labelling techniques combined with IRAS we study in detail the interaction of oxygen with the oxide surfaces, a process of general interest in connection with oxidation reactions. |
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ISSN: | 0920-5861 1873-4308 |
DOI: | 10.1016/S0920-5861(96)00072-7 |