4.8 Article

Disentangling the Photodissociation Dynamics of the HF+ Molecular Radical via Kinetic-Energy-Release-Resolved F 1s Core Excitation and Ionization

期刊

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
卷 12, 期 5, 页码 1390-1395

出版社

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.0c03356

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资金

  1. Bundesministerium fur Bildung und Forschung within the Verbundforschung funding scheme [05K16RG1, 05K16GUC, 05K19RG3, 05K19GU3]
  2. Deutsche Forschungsgemeinschaft [Mu 1068/22, Schi 378/12, SFB925/A3]

向作者/读者索取更多资源

The core level photoionization of the ionic molecular radical HF+ was studied using the photon-ion merged-beams technique, revealing complex ultrafast dissociation dynamics of the F is core hole excited sigma* state. Electronic structure calculations attributed this complex process to a spin-dependent dissociation of the excited sigma* biradical state.
The F is core level photoionization of the ionic molecular radical HF+ has been studied using the photon-ion merged-beams technique at a synchrotron radiation source. Upon analyzing kinetic energy release (KER) dependent photoion yield spectra, complex ultrafast dissociation dynamics of the F is core hole excited sigma* state can be revealed. By means of configuration-interaction electronic structure calculations of the excited molecular potential energy curves, this complex process can be attributed to a spin-dependent dissociation of the excited sigma* biradical state.

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