Core level X-ray photoelectron spectroscopy of RbTiOPO4 and chemical bonding in KTiOPO4, crystal family

Author(s):  
Vladimir K. Makukha ◽  
Viktor V. Atuchin ◽  
Valeriy G. Kesler
2021 ◽  
Author(s):  
Nestor Garcia-Romeral ◽  
Masoomeh Keyhanian ◽  
Angel Morales-Garcia ◽  
Francesc Illas

The relationship between core level binding energy shifts (CLBEs), that can be experimentally determined by X-Ray Photoelectron Spectroscopy, and chemical bonding is analyzed for a series of MXenes, a new...


2018 ◽  
Vol 20 (13) ◽  
pp. 8403-8410 ◽  
Author(s):  
Francesc Viñes ◽  
Carmen Sousa ◽  
Francesc Illas

Core level binding energies, measured by X-ray photoelectron spectroscopy providing unique information regarding the chemical environment of atoms in a system, can be estimated by a diversity of state-of-the-art accurate methods here detailed.


2019 ◽  
Vol 21 (18) ◽  
pp. 9399-9406 ◽  
Author(s):  
Marc Figueras ◽  
Carmen Sousa ◽  
Francesc Illas

The influence of electron correlation into the decomposition of core level binding energy shifts, measured by X-ray photoelectron spectroscopy (XPS), into initial and final effects is analysed for a series of molecules where these effects are noticeable.


2004 ◽  
Vol 95 (4) ◽  
pp. 1963-1968 ◽  
Author(s):  
J. Eng ◽  
I. A. Hubner ◽  
J. Barriocanal ◽  
R. L. Opila ◽  
D. J. Doren

2009 ◽  
Vol 23 (06n07) ◽  
pp. 1910-1915 ◽  
Author(s):  
MIN TENG ◽  
XIAODONG HE ◽  
YUE SUN

SiC films with a quantity of carbon and silicon were obtained by electron beam physical vapor deposition (EB-PVD) from a sintered SiC target with different current intensity of EB. The X-ray photoelectron spectroscopy (XPS) was used for characterization of chemical bonding states of C and Si elements in SiC films in order to study the influence of current intensity of EB on the compositions in the deposited films. At the same time, the nanohardness of the deposited films was investigated.


2011 ◽  
Author(s):  
Y. Miyata ◽  
J. Kanehara ◽  
H. Nohira ◽  
Y. Izumi ◽  
T. Muro ◽  
...  

1993 ◽  
Vol 47 (2) ◽  
pp. 139-149 ◽  
Author(s):  
Lois E. Hamilton ◽  
Peter M. A. Sherwood ◽  
Barbara M. Reagan

The double bonds and aromaticity that impart high thermal stability in fibers often increase the absorption of LTV radiation, resulting in greater susceptibility to photodegradation. This study compares the resistance of three high-performance fibers (Nomex aramid, Kynol novoloid, and PBI) to accelerated light exposure. X-ray photoelectron spectroscopy (XPS) was used to evaluate the photochemical changes on the surfaces of the fibers. On the basis of the C 1 s core-level spectra and oxygen/carbon atomic ratios, the Nomex aramid fibers were photo-oxidized more rapidly than Kynol novoloid and PBI fibers. Similarly, Nomex aramid fibers exhibited more rapid strength losses than the other fibers. We propose that tautomerization inhibited photodegradation in the Kynol novoloid and PBI fibers. XPS core-level and valence-band spectra interpreted by ab initio calculations are shown to be valuable probes of photo-oxidation in fibers.


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