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Träfflista för sökning "WFRF:(Karis O.) ;pers:(Rensmo H.);pers:(Karis O.)"

Sökning: WFRF:(Karis O.) > Rensmo H. > Karis O.

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  • Gorgoi, M, et al. (författare)
  • The high kinetic energy photoelectron spectroscopy facility at BESSY progress and first results
  • 2009
  • Ingår i: Nuclear Instruments and Methods in Physics Research Section A : Accelerators, Spectrometers, Detectors and Associated Equipment. - 0168-9002. ; 601:1-2, s. 48-53
  • Tidskriftsartikel (refereegranskat)abstract
    • Photoelectron spectroscopy at high kinetic energy is a research field that receives an increasing interest due to the possibility of studying bulk properties of materials and deeply buried interfaces. Recently the high kinetic energy electron (HIKE) spectroscopy facility at BESSY in Berlin has become operative at the bending magnet beamline KMC-1. The first results show very good performance. Electron spectra have been recorded using X-ray energies from 2 keV up to 12 keV. Using back-scattering conditions in the crystal monochromator, very high-resolution has been achieved for photon energies around 2, 6 and 8 keV. In the latter case, spectra with a resolving power from the monochromator of >= 80 000 have been achieved and it has been possible to perform electron spectroscopy with resolving power of >= 60 000, yielding a total instrument resolution of about 150 meV as determined directly from spectra. This paper describes the facility and reports some of the first results. (C) 2009 Elsevier B.V. All rights reserved.
  • Johansson, E. M. J., et al. (författare)
  • Valence Electronic Structure Of Ruthenium Based Complexes Probed By Photoelectron Spectroscopy At High Kinetic Energy (Hike) And Modeled By Dft Calculations
  • 2008
  • Ingår i: Chemical Physics Letters. - 0009-2614. ; 464:4-6, s. 192-197
  • Tidskriftsartikel (refereegranskat)abstract
    • The valence electronic structure of a series of molecular films containing ruthenium polypyridine complexes has been investigated by photoelectron spectroscopy (PES) at high kinetic energy (HIKE) using hard X-ray. The experiment shows the possibility to experimentally probe the metal contribution to the valence spectra in a bulk sensitive mode. Specifically to directly follow the Ru 4d contribution to the highest occupied molecular orbitals of such complexes. The experimental spectra are accurately modeled by DFT calculations only if a crystal structure environment is taken into account showing the importance of intermolecular interaction for modeling the electronic structure of such complexes.
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