127 research outputs found
X-ray fluorescence spectra of metals excited below threshold
X-ray scattering spectra of Cu and Ni metals have been measured using
monochromatic synchrotron radiation tuned from far above to more than 10 eV
below threshold. Energy conservation in the scattering process is found to be
sufficient to explain the modulation of the spectral shape, neglecting momentum
conservation and channel interference. At excitation energies close to and
above threshold, the emission spectra map the occupied local partial density of
states. For the sub-threshold excitations, the high-energy flank of the
inelastic scattering exhibits a Raman-type linear dispersion, and an asymmetric
low energy tail develops. For excitation far below threshold the emission
spectra are proportional to a convolution of the occupied and unoccuppied local
partial densities of states.Comment: 10 pages, 3 figures,
http://link.aps.org/doi/10.1103/PhysRevB.68.04511
Intramolecular vibronic dynamics in molecular solids: C60
Vibronic coupling in solid C60 has been investigated with a combination of resonant photoemission spectroscopy (RPES) and resonant inelastic x-ray scattering (RIXS). Excitation as a function of energy within the lowest unoccupied molecular orbital resonance yielded strong oscillations in intensity and dispersion in RPES, and a strong inelastic component in RIXS. Reconciling these two observations establishes that vibronic coupling in this core hole excitation leads to predominantly inelastic scattering and localization of the excited vibrations on the molecule on a femtosecond time scale. The coupling extends throughout the widths of the frontier valence bands.
Vibrational resolved partial cross sections and asymmetry parameters for nitrogen K-shell photoionization of the N2O molecule
Intermanifold similarities in partial photoionization cross sections of helium
Using the eigenchannel R-matrix method we calculate partial photoionization
cross sections from the ground state of the helium atom for incident photon
energies up to the N=9 manifold. The wide energy range covered by our
calculations permits a thorough investigation of general patterns in the cross
sections which were first discussed by Menzel and co-workers [Phys. Rev. A {\bf
54}, 2080 (1996)]. The existence of these patterns can easily be understood in
terms of propensity rules for autoionization. As the photon energy is increased
the regular patterns are locally interrupted by perturber states until they
fade out indicating the progressive break-down of the propensity rules and the
underlying approximate quantum numbers. We demonstrate that the destructive
influence of isolated perturbers can be compensated with an energy-dependent
quantum defect.Comment: 10 pages, 10 figures, replacement with some typos correcte
Electronic structure of Co_xTiSe_2 and Cr_xTiSe_2
The results of investigations of intercalated compounds Cr_xTiSe_2 and
Co_xTiSe_2 by X-ray photoelectron spectroscopy (XPS) and X-ray emission
spectroscopy (XES) are presented. The data obtained are compared with
theoretical results of spin-polarized band structure calculations. A good
agreement between theoretical and experimental data for the electronic
structure of the investigated materials has been observed. The interplay
between the M3d--Ti3d hybridization (M=Cr, Co) and the magnetic moment at the M
site is discussed. A 0.9 eV large splitting of the core Cr2p{3/2} level was
observed, which reveals a strong exchange magnetic interaction of 3d-2p
electrons of Cr. In the case of a strong localization of the Cr3d electrons
(for x<0.25), the broadening of the CrL spectra into the region of the states
above the nominal Fermi level was observed and attributed to X-ray re-emission.
The measured kinetic properties are in good accordance with spectral
investigations and band calculation results.Comment: 14 pages, 11 figures, submitted to Phys.Rev.
Erratum Ground state potential energy surfaces around selected atoms from resonant inelastic x ray scattering
Scientific Reports6 20054; doi 10.1038 srep20054; published online 29 January 2016; updated 30 June 2017The original HTML version of this Article listed an incorrect volume number. This has now been corrected in the HTML version; the PDF version was correct at the time of publicatio
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