| 1. |
- Guo, J. H., et al.
(författare)
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X-ray emission spectroscopy of hydrogen bonding and electronic structure of liquid water
- 2002
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Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 89:13
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Tidskriftsartikel (refereegranskat)abstract
- We use x-ray emission spectroscopy to examine the influence of the intermolecular interaction on the local electronic structure of liquid water. By comparing x-ray emission spectra of the water molecule and liquid water, we find a strong involvement of the a(1)-symmetry valence-orbital in the hydrogen bonding. The local electronic structure of water molecules, where one hydrogen bond is broken at the hydrogen site, is separately determined. Our results provide an illustration of the important potential of x-ray emission spectroscopy for elucidating basic features of liquids.
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| 2. |
- Kashtanov, Stepan, et al.
(författare)
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Local structures of liquid water studied by x-ray emission spectroscopy
- 2004
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Ingår i: Physical Review B. Condensed Matter and Materials Physics. - 1098-0121 .- 1550-235X. ; 69:2
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Tidskriftsartikel (refereegranskat)abstract
- The O Kalpha x-ray emission spectra of water clusters with different sizes and conformations embedded in a continuum medium are simulated. The calculations have successfully explained the experimental spectra of water in both gas and liquid phases. It is shown that the x-ray emission spectra are very sensitive to the local hydrogen bonding structures. Strong electron sharing between different water molecules is observed and its possible connection to the covalency of hydrogen bonding is discussed. The experimentally observed strong excitation energy dependence of the spectra has been interpreted in terms of the polarization and angular dependence for the gas phase, and in terms of variations of local hydrogen bonding structures for the liquid phase.
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| 3. |
- Kitajima, M., et al.
(författare)
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Doppler effect in resonant photoemission from SF6 : Correlation between doppler profile and auger emission anisotropy
- 2003
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Ingår i: Physical Review Letters. - 0031-9007 .- 1079-7114. ; 91:21
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Tidskriftsartikel (refereegranskat)abstract
- Fragmentation of the SF6 molecule upon F 1s excitation has been studied by resonant photoemission. The F atomiclike Auger line exhibits the characteristic Doppler profile that depends on the direction of the photoelectron momentum relative to the polarization vector of the radiation as well as on the photon energy. The measured Doppler profiles are analyzed by the model simulation that takes account of the anisotropy of the Auger emission in the molecular frame. The Auger anisotropy extracted from the data decreases with an increase in the F-SF5 internuclear distance.
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| 4. |
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| 5. |
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| 6. |
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| 7. |
- Sałek, P., et al.
(författare)
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Resonant X-ray Raman scattering involving avoided crossings in the final-state potential-energy curves
- 2000
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Ingår i: Physical Review A - Atomic, Molecular, and Optical Physics. - 1050-2947. ; 62:6, s. 62501-62506
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Tidskriftsartikel (refereegranskat)abstract
- The effect of avoided crossings on the spectral profiles of resonant X-ray Raman scattering was investigated. The theory was also applied to nitrogen molecule in the core-excited level to analyze the electron decay process. The dependence of internuclear distance on electron transition amplitude was considered important with respect to the breakdown process of the transition. The correlation between the nuclear and electronic degrees of freedom was also reported.
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| 8. |
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| 9. |
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| 10. |
- Björneholm, O., et al.
(författare)
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Doppler splitting of in-flight auger decay of dissociating oxygen molecules : The localization of delocalized core holes
- 2000
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Ingår i: Physical Review Letters. - : AMERICAN PHYSICAL SOC. - 0031-9007 .- 1079-7114. ; 84:13, s. 2826-2829
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Tidskriftsartikel (refereegranskat)abstract
- By exploiting the core-excitation-induced dissociation of O-2, we find that the Auger emission exhibits a Doppler-like energy shift. We show this to be a manifestation of localization of the core hole and propose that the problem of core-hole localization versus delocalization in core-hole spectroscopies may be resolved by considering the nature of the measurement.
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