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Resonant and nonresonant x-ray scattering spectra of some poly(phenylenevinylene)s

Guo, J.-H. (author)
Uppsala University
Magnuson, Martin, 1965- (author)
Uppsala University
Såthe, C. (author)
Uppsala University
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Nordgren, J. (author)
Uppsala University
Yang, L. (author)
Linköpings universitet,Beräkningsfysik,Tekniska högskolan
Luo, Y. (author)
Linköpings universitet,Beräkningsfysik,Tekniska högskolan
Ågren, H. (author)
Linköpings universitet,Beräkningsfysik,Tekniska högskolan
Xing, K. Z. (author)
Linköpings universitet,Ytors Fysik och Kemi,Tekniska högskolan
Johansson, N. (author)
Linköpings universitet,Ytors Fysik och Kemi,Tekniska högskolan
Salaneck, William R. (author)
Linköpings universitet,Ytors Fysik och Kemi,Tekniska högskolan
Daik, R. (author)
Durham University
Feast, W. J. (author)
Durham University
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 (creator_code:org_t)
AIP Publishing, 1998
1998
English.
In: Journal of Chemical Physics. - : AIP Publishing. - 0021-9606 .- 1089-7690. ; 108:14, s. 5990-5996
  • Journal article (peer-reviewed)
Abstract Subject headings
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  • The electronic structure of some poly(phenylenevinylene)s have been investigated by resonant and nonresonant x-ray inelastic scattering spectroscopies. The nonresonant as well as all resonant spectra for each polymer demonstrate benzene-like features, indicating a local character of the x-ray emission in which the phenyl ring acts as a building block. Theoretical simulations of x-ray energies and intensities taking the repeat unit as a model molecule of the polymer agree with the experimental spectra fairly well. The edges of the occupied bands have been identified in the nonresonant spectra of each polymer. By subtracting the emission energy of the highest occupied molecular orbital in the nonresonant spectrum from the core excitation energy in the resonant spectrum an alternative way to determine the optical band gap is obtained. As for free benzene the outer π band in the polymer spectra show a depletion of the emission going from the nonresonant to the resonant x-ray emission spectra. It is demonstrated that this transition, which is strictly symmetry forbidden for free benzene, becomes effectively forbidden in the polymer case as a result of strong interference effects, and it is argued that this is the general case for resonant x-ray emission of conjugated polymers as far as the frozen orbital approximation holds.

Keyword

Polymers
elastomers
and plastics
X-ray emission spectra and fluorescence
Electron density of states and band structure of crystalline solids
NATURAL SCIENCES
NATURVETENSKAP

Publication and Content Type

ref (subject category)
art (subject category)

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