Free molecules undergo processes with photons; in particular, they can undergo photoionization and photodissociation, which are relevant processes in nature and laboratory. Recently, it has been shown that in a cavity, the reverse process of photoionization, namely, electron capture becomes highly probable. The underlying mechanism is the formation of a hybrid resonance state.
View Article and Find Full Text PDFWe report the experimental observation of quantum interference in the nuclear wave-packet dynamics driving ultrafast excitation-energy transfer in argon dimers below the threshold of interatomic Coulombic decay (ICD). Using time-resolved photoion-photoion coincidence spectroscopy and quantum dynamics simulations, we reveal that the electronic relaxation dynamics of the inner-valence 3s hole on one atom leading to a 4s or 4p excitation on the other one is influenced by nuclear quantum dynamics in the initial state, giving rise to a deep, periodic modulation on the kinetic-energy-release (KER) spectra of the coincident Ar^{+}-Ar^{+} ion pairs. Moreover, the time-resolved KER spectra show characteristic fingerprints of quantum interference effects during the energy-transfer process.
View Article and Find Full Text PDFThe interaction of atoms and molecules with quantum light as realized in cavities has become a highly topical and fast growing research field. This interaction leads to hybrid light-matter states giving rise to new phenomena and opening up pathways to control and manipulate properties of the matter. Here, we substantially extend the scope of the interaction by allowing free electrons to enter the cavity and merge and unify the two active fields of electron scattering and quantum-light-matter interaction.
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