scholarly journals Specific chemical bond relaxation unravelled by analysis of shake-up satellites in the oxygen single site double core hole spectrum of CO2

Author(s):  
Anthony Ferté ◽  
Francis Penent ◽  
Jérôme Palaudoux ◽  
Hiroshi Iwayama ◽  
Eiji Shigemasa ◽  
...  

We recently developed a method dubbed NOTA+CIPSI [A. Ferté, et al., J. Phys. Chem. Lett. 11, 4359 (2020)] to compute single site double core hole (ssDCH or K−2 ) spectra,...

1992 ◽  
Vol 164 (1) ◽  
pp. 73-82 ◽  
Author(s):  
P. Decleva ◽  
M. Ohno
Keyword(s):  
The Core ◽  

2017 ◽  
Vol 1 (8) ◽  
pp. 1573-1579 ◽  
Author(s):  
Madoka Yamaguchi ◽  
Shunichiro Ito ◽  
Amane Hirose ◽  
Kazuo Tanaka ◽  
Yoshiki Chujo

The control of luminescence properties between fluorescence aggregation-caused quenching and aggregation-induced emission with or without a chemical bond at a single site in boron complexes was accomplished.


Author(s):  
E. A. Kenik ◽  
J. Bentley

Cliff and Lorimer (1) have proposed a simple approach to thin foil x-ray analy sis based on the ratio of x-ray peak intensities. However, there are several experimental pitfalls which must be recognized in obtaining the desired x-ray intensities. Undesirable x-ray induced fluorescence of the specimen can result from various mechanisms and leads to x-ray intensities not characteristic of electron excitation and further results in incorrect intensity ratios.In measuring the x-ray intensity ratio for NiAl as a function of foil thickness, Zaluzec and Fraser (2) found the ratio was not constant for thicknesses where absorption could be neglected. They demonstrated that this effect originated from x-ray induced fluorescence by blocking the beam with lead foil. The primary x-rays arise in the illumination system and result in varying intensity ratios and a finite x-ray spectrum even when the specimen is not intercepting the electron beam, an ‘in-hole’ spectrum. We have developed a second technique for detecting x-ray induced fluorescence based on the magnitude of the ‘in-hole’ spectrum with different filament emission currents and condenser apertures.


1989 ◽  
Vol 86 ◽  
pp. 853-859 ◽  
Author(s):  
Federico Moscardó ◽  
José Pérez-Jordá ◽  
Emilio San-Fabián

1986 ◽  
Vol 47 (C8) ◽  
pp. C8-961-C8-964
Author(s):  
E. BEAUREPAIRE ◽  
F. LE NORMAND ◽  
G. KRILL

2017 ◽  
Author(s):  
B Redwan ◽  
C Biancosino ◽  
G Wöbker ◽  
F Giebel ◽  
R Zanner ◽  
...  
Keyword(s):  

2003 ◽  
Vol 773 ◽  
Author(s):  
Mo Yang ◽  
Shalini Prasad ◽  
Xuan Zhang ◽  
Mihrimah Ozkan ◽  
Cengiz S. Ozkan

AbstractExtracellular potential is an important parameter which indicates the electrical activity of live cells. Membrane excitability in osteoblasts plays a key role in modulating the electrical activity in the presence of chemical agents. The complexity of cell signal makes interpretation of the cellular response to a chemical agent very difficult. By analyzing shifts in the signal power spectrum, it is possible to determine a frequency spectrum also known as Signature Pattern Vectors (SPV) specific to a chemical. It is also essential to characterize single cell sensitivity and response time for specific chemical agents for developing detect-to-warn biosensors. We used a 4x4 multiple Pt microelectrode array to spatially position single osteoblast cells, by using a gradient AC field. Fast Fourier Transformation (FFT) and Wavelet Transformation (WT) analyses were used to extract information pertaining to the frequency of firing from the extracellular potential.


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