1. |
- Bjorneholm, O, et al.
(author)
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Femtosecond dissociation of core-excited HCl monitored by frequency detuning
- 1997
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In: PHYSICAL REVIEW LETTERS. - : AMER INST PHYSICS. - 0031-9007. ; 79:17, s. 3150-3153
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Journal article (other academic/artistic)abstract
- Core excitation of gaseous HCl to the dissociative sigma* state leads to a deexcitation spectrum with two qualitatively different contributions-a broad molecular background and narrow atomic lines. The experiment demonstrates that the ratio of integrated
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2. |
- Carravetta, V, et al.
(author)
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Excitation-energy-dependent resonant photoemission: C1s-pi* spectra of carbon monoxide
- 1997
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In: PHYSICAL REVIEW A. - : AMER INST PHYSICS. - 1050-2947. ; 56:6, s. 4665-4674
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Journal article (other academic/artistic)abstract
- High-resolution measurements of the x-ray resonant photoemission of CO near the C1s-->pi* transition are presented. The branching ratios for the valence shell ionization close to the resonance how a strong dependence on the photon energy with a clear asym
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3. |
- deBrito, AN, et al.
(author)
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Auger decay of the molecular field split S 2p core excited states in HS radical
- 1997
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In: JOURNAL OF CHEMICAL PHYSICS. - : AMER INST PHYSICS. - 0021-9606. ; 106:1, s. 18-23
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Journal article (other academic/artistic)abstract
- Using synchrotron radiation, very high resolution electron spectra at the 2p --> 6a(1) and 2p --> 3b(2) resonances of H2S have been recorded. Auger transitions from molecular field split S 2p hole states of HS* fragment, created by fast dissociation of th
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4. |
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5. |
- Sundin, S, et al.
(author)
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Auger decay of core-excited higher Rydberg states of carbon monoxide
- 1997
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In: JOURNAL OF PHYSICS B-ATOMIC MOLECULAR AND OPTICAL PHYSICS. - : IOP PUBLISHING LTD. - 0953-4075. ; 30:19, s. 4267-4278
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Journal article (other academic/artistic)abstract
- The de-excitation of higher core-excited C 1s(-1)np Rydberg states of carbon monoxide has been studied. It is found that already with a main quantum number of 4 or higher, Rydberg states of p-symmetry can be successfully treated within the single-particle
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