Authors
Lukas Weise, Steve Takouan Tchounga, Bernd von Issendorff
Published in
Chemphyschem : a European journal of chemical physics and physical chemistry. Volume 27. Issue 20. Oct 28, 2026.
Abstract
Angle-resolved photoelectron spectroscopy (ARPES) has been used to probe the electronic and vibrational structure of the cluster. High-resolution spectra recorded near the detachment threshold reveal well-resolved vibrational progressions, enabling a precise determination of the adiabatic electron affinity (EA = 1.8947(12) eV). Measured vibrational frequencies are in good agreement with density-functional-theory predictions, allowing the assignment of the observed modes. The anisotropy parameter of the photoelectron angular distribution from the highest occupied molecular orbital follows the universal momentum-dependent behaviour recently predicted. In some cases exhibits a dependence on the final vibrational excitation of the cluster which deviates from the prediction, revealing a possible influence of autoionizing excited states.
PMID:
42927984
Bibliographic data and abstract were imported from PubMed on 26 Oct 2026.
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