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Resonant inelastic soft X-ray scattering spectra at the nitrogen and carbon K-edges of poly(pyridine-2,5-diyl)
Uppsala University.ORCID iD: 0000-0002-0317-0190
Linköping University, Department of Physics, Chemistry and Biology, Computational Physics. Linköping University, The Institute of Technology.
Uppsala University.
Uppsala University.
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1999 (English)In: Journal of Electron Spectroscopy and Related Phenomena, ISSN 0368-2048, Vol. 101-103, 573-578 p.Article in journal (Refereed) Published
Abstract [en]

Resonant inelastic scattering measurements of the conjugated polymer, poly(pyridine-2,5-diyl) have been performed at the nitrogen and carbon K-edges using synchrotron radiation. For comparison, molecular orbital calculations of the spectra have been carried out with the repeat unit as a model molecule of the polymer chain. The resonant emission spectra show depletion of the π electron bands which is consistent with symmetry selection and momentum conservation rules. The depletion is most obvious in the resonant inelastic scattering spectra of carbon while the nitrogen spectra are dominated by lone pair n orbital emission of σ symmetry and are less excitation energy dependent. By comparing the measurements to calculations an isomeric dependence of the resonant spectra is found giving preference to two of the four possible isomers in the polymer.

Place, publisher, year, edition, pages
1999. Vol. 101-103, 573-578 p.
National Category
Natural Sciences
URN: urn:nbn:se:liu:diva-54985DOI: 10.1016/S0368-2048(98)00354-5OAI: diva2:312908
Available from: 2010-04-26 Created: 2010-04-26 Last updated: 2013-10-02
In thesis
1. Electronic Structure Studies Using Resonant X-ray and Photemission Spectroscopy
Open this publication in new window or tab >>Electronic Structure Studies Using Resonant X-ray and Photemission Spectroscopy
1999 (English)Doctoral thesis, comprehensive summary (Other academic)
Abstract [en]

This thesis addresses the electronic structure of molecules and solids using resonant X-ray emission and photoemission spectroscopy. The use of monochromatic synchrotron radiation and the improved performance of the instrumentation have opened up the possibility of detailed analyses of the response of the electronic systems under interaction with X-rays. The experimental studies are accompanied by numerical ab initio calculations in the formalism of resonant inelastic scattering. The energy selectivity has made it possible for the first time to study how the chemical bonds in a molecule break up during resonant inelastic X-ray scattering. In the conjugated polymer systems, the element selectivity of the X-ray emission process made it possible to probe the different atomic elements separately. The X-ray emission technique proved to be useful for extracting isomeric information, and for measuring the change in the valence levels at different degrees of doping. In this thesis, spectral satellite features in transition metals were thoroughly investigated for various excitation energies around a core-level threshold. By measuring the relative spectral intensity of the satellites it was possible to extract information on the partial core-level widths. Using the nickel metal system as an example, it was shown that it is possible to probe the different core-excited states close toshake-up thresholds by measuring the relative spectral intensity variation of the Auger emission.Resonant photoemission measurements showed unambiguous evidence of interference effects. Theseeffects were also thoroughly probed using angle-dependent measurements. The combination of X-rayemission and absorption were useful for studying buried layers and interfaces due to the appreciable penetration depth of soft X-rays. X-ray scattering was further found to be useful for studying low-energy excited states of rare earth metallic compounds and transition metal oxides.

Place, publisher, year, edition, pages
Uppsala: Uppsala University, 1999
, Acta Universitatis Upsaliensis, ISSN 1104-232X ; 452
Electronic structure, resonant x-ray emission, photoemission spectroscopy
National Category
Physical Sciences
urn:nbn:se:liu:diva-56480 (URN)91-554-4463-6 (ISBN)
Public defence
Available from: 2010-05-19 Created: 2010-05-18 Last updated: 2013-11-14Bibliographically approved

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