ChemInform Abstract: LOW-ENERGY PHOTOELECTRON SPECTROSCOPY OF SOLIDS. ELECTRONIC STRUCTURE OF THE CYANIDE, NITRITE, AND NITRATE IONS

1977 ◽  
Vol 8 (34) ◽  
pp. no-no
Author(s):  
M. CONSIDINE ◽  
J. A. CONNOR ◽  
I. H. HILLIER
2005 ◽  
Vol 483-485 ◽  
pp. 547-550 ◽  
Author(s):  
Konstantin V. Emtsev ◽  
Thomas Seyller ◽  
Lothar Ley ◽  
A. Tadich ◽  
L. Broekman ◽  
...  

We have investigated Si-rich reconstructions of 4H-SiC( 00 1 1 ) surfaces by means of low-energy electron diffraction (LEED), x-ray photoelectron spectroscopy (XPS), and angleresolved ultraviolet photoelectron spectroscopy (ARUPS). The reconstructions of 4H-SiC( 00 1 1 ) were prepared by annealing the sample at different temperatures in a flux of Si. Depending on the temperature different reconstructions were observed: c(2×2) at T=800°C, c(2×4) at T=840°C. Both reconstructions show strong similarities in the electronic structure.


2009 ◽  
Vol 80 (9) ◽  
Author(s):  
T. Claesson ◽  
M. Månsson ◽  
A. Önsten ◽  
M. Shi ◽  
Y. Sassa ◽  
...  

2020 ◽  
Author(s):  
Samer Gozem ◽  
Robert Seidel ◽  
Uwe Hergenhahn ◽  
Evgeny Lugovoy ◽  
Bernd Abel ◽  
...  

<div>We report a combined experimental and theoretical study of bulk water photoionization. Angular distributions of photoelectrons produced by ionizing the valence band of neat water using X-ray radiation (250-750 eV) show a limited (<30 %) decrease in the beta anisotropy parameter compared to the gas phase, indicating that the electronic structure of the individual water molecules can be probed. By theoretical modeling using high-level electronic structure methods, we show that in a high-energy regime photoionization of bulk can be described as an incoherent superposition of individual molecules, in contrast to a low-energy regime where photoionization probes delocalized entangled states of molecular aggregates. The two regimes-low energy versus high energy-are defined as limiting cases where the de Broglie wavelength of the photoelectron is either larger or smaller than the intermolecular distance between water molecules, respectively. The comparison of the measured and computed anisotropies reveals that at high kinetic energies the observed reduction in beta is mostly due to scattering rather than rehybridization due to solvation.</div>


2020 ◽  
Author(s):  
Samer Gozem ◽  
Robert Seidel ◽  
Uwe Hergenhahn ◽  
Evgeny Lugovoy ◽  
Bernd Winter ◽  
...  

<div>We report a combined experimental and theoretical study of bulk water photoionization. Angular distributions of photoelectrons produced by ionizing the valence band of neat water using X-ray radiation (250-750 eV) show a limited (<30 %) decrease in the beta anisotropy parameter compared to the gas phase, indicating that the electronic structure of the individual water molecules can be probed. By theoretical modeling using high-level electronic structure methods, we show that in a high-energy regime photoionization of bulk can be described as an incoherent superposition of individual molecules, in contrast to a low-energy regime where photoionization probes delocalized entangled states of molecular aggregates. The two regimes-low energy versus high energy-are defined as limiting cases where the de Broglie wavelength of the photoelectron is either larger or smaller than the intermolecular distance between water molecules, respectively.</div>


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Mahdi Hajlaoui ◽  
Stefano Ponzoni ◽  
Michael Deppe ◽  
Tobias Henksmeier ◽  
Donat Josef As ◽  
...  

AbstractQuantum well (QW) heterostructures have been extensively used for the realization of a wide range of optical and electronic devices. Exploiting their potential for further improvement and development requires a fundamental understanding of their electronic structure. So far, the most commonly used experimental techniques for this purpose have been all-optical spectroscopy methods that, however, are generally averaging in momentum space. Additional information can be gained by angle-resolved photoelectron spectroscopy (ARPES), which measures the electronic structure with momentum resolution. Here we report on the use of extremely low-energy ARPES (photon energy ~ 7 eV) to increase depth sensitivity and access buried QW states, located at 3 nm and 6 nm below the surface of cubic-GaN/AlN and GaAs/AlGaAs heterostructures, respectively. We find that the QW states in cubic-GaN/AlN can indeed be observed, but not their energy dispersion, because of the high surface roughness. The GaAs/AlGaAs QW states, on the other hand, are buried too deep to be detected by extremely low-energy ARPES. Since the sample surface is much flatter, the ARPES spectra of the GaAs/AlGaAs show distinct features in momentum space, which can be reconducted to the band structure of the topmost surface layer of the QW structure. Our results provide important information about the samples’ properties required to perform extremely low-energy ARPES experiments on electronic states buried in semiconductor heterostructures.


2020 ◽  
Author(s):  
Samer Gozem ◽  
Robert Seidel ◽  
Uwe Hergenhahn ◽  
Evgeny Lugovoy ◽  
Bernd Abel ◽  
...  

<div>We report a combined experimental and theoretical study of bulk water photoionization. Angular distributions of photoelectrons produced by ionizing the valence band of neat water using X-ray radiation (250-750 eV) show a limited (<30 %) decrease in the beta anisotropy parameter compared to the gas phase, indicating that the electronic structure of the individual water molecules can be probed. By theoretical modeling using high-level electronic structure methods, we show that in a high-energy regime photoionization of bulk can be described as an incoherent superposition of individual molecules, in contrast to a low-energy regime where photoionization probes delocalized entangled states of molecular aggregates. The two regimes-low energy versus high energy-are defined as limiting cases where the de Broglie wavelength of the photoelectron is either larger or smaller than the intermolecular distance between water molecules, respectively. The comparison of the measured and computed anisotropies reveals that at high kinetic energies the observed reduction in beta is mostly due to scattering rather than rehybridization due to solvation.</div>


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