Spectroscopic analysis reveals 4f electrons influence metal–metal bonds in cerium dimers, suggesting new bonding strategies.
Direct metal–metal bonding between lanthanide atoms has been challenging to observe. We report on the first spectroscopic characterization of the cerium dimer anion (Ce2–) and its neutral analog (Ce2) in the gas phase, achieved using photoelectron and ultrafast spectroscopy combined with high-level quantum chemistry calculations. The electron affinity of Ce2 is 0.24 eV, from which a dissociation energy of 2.21 eV is derived for Ce2–. The wave-packet dynamics upon photodetachment are studied and yield vibrational frequencies for electronically excited Ce2. Ce2– exhibits a conventional metal–metal triple bond with minimal contribution from 4f electrons. However, evidence of 4f-electron participation in bonding is identified for the low-energy excited states only 0.1 eV higher. The results challenge the assumption of inert 4f electrons in metal–metal bonding, and we propose a promising strategy for forming stable lanthanide–lanthanide bonds involving significant 4f-electron contributions.
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Jin et al. (2025) studied this question.
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