Systematics in the core level spectra of Th-intermetallics

1986 ◽  
Vol 63 (3) ◽  
pp. 305-311 ◽  
Author(s):  
D. D. Sarma ◽  
F. U. Hillebrecht ◽  
O. Gunnarsson ◽  
K. Sch�nhammer
Keyword(s):  
1998 ◽  
Vol 4 (S2) ◽  
pp. 766-767
Author(s):  
D. A. Muller

The role of core level shifts at metallic interfaces has often been ignored in electron energy loss spectroscopy (EELS) even though very small changes in bond length can lead to large core level shifts. However, the popular interpretation of core level shifts as measures of charge transfer is highly problematic. For instance, in binary alloys systems, the core level shifts can be the same sign for both atomic constituents[l]. The simple interpretation would require that both atomic species had lost or gained charge. Further, the signs of the core level shifts can be opposite to those expected from electronegativity arguments[2]. A core level shift (CLS) is still possible, even when no charge transfer occurs. As illustrated in Fig. 1, if the valence band width is increased, the position of the center of the valence band with respect to the Fermi energy will change (as the number of electrons remains unchanged).


1992 ◽  
Vol 283 ◽  
Author(s):  
Hisao Nakashima ◽  
Koichi Inoue ◽  
Kenzo Maehashi

ABSTRACTSi2p core level absorption and photoemission spectra are taken for different porous Si layers using synchrotron radiation, toknow the electronic structures of porous Si. The core level absorption spectra show the high energy shift of the conduction band which correlates with the photo-luminescence blue shift. The oxidation states of porous Si are clarified from the photoemission spectra.


1993 ◽  
Vol 47 (1) ◽  
pp. 361-373 ◽  
Author(s):  
E. Hudson ◽  
D. A. Shirley ◽  
M. Domke ◽  
G. Remmers ◽  
A. Puschmann ◽  
...  
Keyword(s):  

2015 ◽  
Vol 17 (37) ◽  
pp. 24349-24355 ◽  
Author(s):  
Roberto Carlos Salvarezza ◽  
Pilar Carro

DFT calculations show that the core level shift (CLS) of the S 2p binding energy of thiol and sulfur atoms on different thiol–Pd(111) surfaces strongly depends on the adsorbed or subsurface state of sulfur atoms.


1993 ◽  
Vol 207 (4-6) ◽  
pp. 569-574 ◽  
Author(s):  
Paul S. Bagus ◽  
Gianfranco Pacchioni ◽  
Fulvio Parmigiani
Keyword(s):  

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