Andreas C. Cangellaris, Karen M. Coperich, et al.
EMC 2001
The interaction of oxygen with polycrystalline cobalt surfaces has been studied at 300 K (1 × 10-6 to 1 × 10-5 Torr) using high-resolution (monochromatized) X-ray photoemission. At high exposures (> 100 L nominal) CoO is identified as the product from the nature of the Co 2p 3 2, 2p 1 2, 3s, and valence band spectra. There is no evidence for measurable amounts of Co3O4 or Co2O3. Two O 1s features are observed at both high and low (10L) exposures. The dominant O 1s feature at 529.5 ± 0.2 eV corresponds to the oxide and a minor feature at 531.3 ± 0.2 eV is attributed to non-stoichiometric surface oxygen. Exposure to air produces quite different results, with a dominant O 1s feature at 531.5 ± 0.2 eV and dominant Co 2p 3 2 and 2p 1 2 features centered at 781.3 ± 0.2 eV and 797.1 ± 0.2 eV. These three values are very close to those reported here for bulk Co(OH)2. Ion etching of the air-exposed surface removes this dominant surface product rapidly revealing some oxide and finally metal. © 1976.
Andreas C. Cangellaris, Karen M. Coperich, et al.
EMC 2001
Mark W. Dowley
Solid State Communications
Elizabeth A. Sholler, Frederick M. Meyer, et al.
SPIE AeroSense 1997
T. Schneider, E. Stoll
Physical Review B