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Sökning: WFRF:(Kivimaki M) > Kungliga Tekniska Högskolan

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1.
  • Kivimaki, A., et al. (författare)
  • Fluorescence emission at core-to-Rydberg excitations in the N-2 molecule
  • 2009
  • Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 42:18
  • Tidskriftsartikel (refereegranskat)abstract
    • Fluorescence emission at the N 1s edge of the N-2 molecule has been studied with synchrotron radiation excitation. The partial fluorescence yields in the ultraviolet (250-320 nm) and visible (300-650 nm) wavelengths were collected by scanning the photon energy across the core-to-Rydberg excitations and the N 1s ionization potential (IP). When compared to the total ion yield, both fluorescence yields are most enhanced at the excitations to high Rydberg orbitals. A discrete structure appears just below the N 1s IP only in the UV yield and is assigned to core-valence doubly excited states. Dispersed fluorescence spectra in selected wavelength windows were measured at several photon energies in order to find out which fragments are responsible for the enhancement of fluorescence emission just below the N 1s IP. The excitation functions determined and considerations on de-excitation pathways indicate that the main responsible is the N+ ion.
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2.
  • Kivimaki, A., et al. (författare)
  • Line shape narrowing in the ultraviolet yield at the N 1s -> pi* resonance of the N-2 molecule
  • 2009
  • Ingår i: Journal of Physics B. - : IOP Publishing. - 0953-4075 .- 1361-6455. ; 42:7
  • Tidskriftsartikel (refereegranskat)abstract
    • The intensity of fluorescence emission in the wavelength region of 250-320 nm has been measured across the N 1s -> pi* resonance of the N-2 molecule. It displays a narrower line shape than the total ion yield recorded simultaneously. We explain the finding by the particularities of the resonant Auger transitions from the N 1s(-1) pi* state to the D-2 Pi(g) state in N-2(+) and by the subsequent D-2 Pi(g) -> A(2)Pi(u) emission.
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3.
  • Ruiz, J. A., et al. (författare)
  • Autoionisation of superexcited states in N-2 to the N2+B state
  • 2003
  • Ingår i: Chemical Physics Letters. - : Elsevier BV. - 0009-2614 .- 1873-4448. ; 372:02-jan, s. 139-146
  • Tidskriftsartikel (refereegranskat)abstract
    • Vibrationally resolved N-2(+) (B-X) (1-2) and (0-1) emission bands were recorded after photoexcitation of N-2 in the 20-46 eV energy range. The branching ratio between these transitions reveals strong non-Franck-Condon effects. Ab initio calculations using a configuration interaction method based on Kohn-Sham orbitals indicate that the autoionisation of certain superexcited states is responsible for some structures present in the branching ratio curve.
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5.
  • Stankiewicz, M., et al. (författare)
  • Relaxation dynamics of SF6 studied by energy-resolved electron ion coincidence technique
  • 2004
  • Ingår i: Journal of Electron Spectroscopy and Related Phenomena. - : Elsevier BV. - 0368-2048 .- 1873-2526. ; 137-40, s. 369-375
  • Tidskriftsartikel (refereegranskat)abstract
    • The mass spectra from the SF6 molecule acquired by energy-resolved electron ion coincidence (EREICO) technique using (1t(1g) + [5t(1u),1t(2u)]), (3e(g) + 1t(2g)), 4t(1u), and 5a(1g) electrons after both valence and S 2p(-1) 6a(1g) core excitation reveal a strong selectivity in the dissociation from these states. From the comparison of the obtained spectra, the influence of the core-excited state in the relaxation pathway of the molecule is studied. The S 2p --> 6a(1g) core excitation does not affect the relaxation dynamics after participator Auger decay to the (1t(1g) + [5t(1u),1t(2u)])(-1) and (4t(1u))(-l) states, but it alters the relaxation dynamics after participator Auger decay to the (3e(g) + 1t(2g))(-1) and (5a(1g))(-1) states with respect to the decay processes after direct excitation of the same orbitals. These observations point to core excitation induced dissociation in the SF6 molecule.
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  • Resultat 1-5 av 5

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