A study of the core electron binding energies of ozone by x-ray photoelectron spectroscopy and the Xα scattered wave method

1977 ◽  
Vol 49 (2) ◽  
pp. 213-217 ◽  
Author(s):  
M.Salim Banna ◽  
David C. Frost ◽  
Charles A. McDowell ◽  
Louis Noodleman ◽  
Barry Wallbank
1992 ◽  
Vol 7 (8) ◽  
pp. 1984-1986 ◽  
Author(s):  
Shigemi Kohiki ◽  
Mikihiko Nishitani ◽  
Takayuki Negami ◽  
Takahiro Wada

The Cu, In, and Se core-level electron binding energies of the p-type Cu–In–Se–N thin film were larger than those of the n-type Cu–In–Se thin film. The positive shift of the core-electron binding energies for the Cu–In–Se–N film is consistent with that expected from the conduction types of the films. Holes were positioned in the Cu–Se antibonding orbitals of the Cu–In–Se–N film. The analysis using the Auger parameter revealed that the Cu–Se bonding interaction is stronger for the Cu–In–Se–N film than for the Cu–In–Se film.


Clay Minerals ◽  
1982 ◽  
Vol 17 (4) ◽  
pp. 477-481 ◽  
Author(s):  
S. Evans ◽  
E. Raftery

It is usually assumed that the oxidation state of the small proportion of Mn sometimes present in micas is +2, although there is evidence from electronic spectroscopy (Burns, 1970) for at least the occasional occurrence of Mn(III) in manganophyllite. We describe here X-ray photoelectron spectroscopic (XPS) measurements on the Mn in a Norwegian lepidolite which was the subject of a concurrent structural study by X-ray photoelectron diffraction (Evans & Raftery, 1982). To establish the Mn oxidation state we have compared the Mn2p core-electron binding energies (BE), the Mn2P3/2-O ls BE differences, and the Mn2p XPS peak profiles from the four common oxides of manganese (MnO, Mn3O4, Mn2O3 and MnO2) with those from the lepidolite. A re-examination of these oxides was undertaken because the agreement between reports in the literature was unsatisfactory, and uncertainty existed concerning the integrity of some of the surfaces previously examined.


1988 ◽  
Vol 53 (3) ◽  
pp. 425-432 ◽  
Author(s):  
Zdeněk Bastl ◽  
Heidrun Gehlmann

The core electron binding energies of eighteen compounds containing iodine in different oxidation states ranging from (-I) to (VII) have been measured. The observed chemical shifts differ from the literature data. The anticipated existence of hexavalent iodine in certain compounds has not been demonstrated. The relative subshell photoemission intensities of iodine have been determined. Empirically derived atomic sensitivity factors and theoretical photoionization cross-sections have been used to calculate the surface stoichiometry. The concentration ratios obtained via the two methods are compared. In agreement with generally accepted view the results of this comparison imply that, for quantitative surface analysis, empirical values should be used rather than theoretical data.


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