Time-resolved solvation dynamics of Li ⁺ , Na ⁺ and K ⁺ ions in liquid helium nanodroplets

In 2023, ultrafast pump-probe spectroscopy was used to record the solvation dynamics of a single Na⁺ ion in a liquid helium droplet, atom-by-atom and with femtosecond time resolution [Albrechtsen <i>et al., Nature</i>, 2023, <b>623</b>, 319]. Subsequently, theoretical studies showed that other alkali ions solvate in a similar manner but no experimental results have been reported so far. Here, we extend the previous measurement on Na⁺ to Li⁺ and K⁺ ions. A pump pulse selectively ionizes an alkali atom, initially residing at the droplet surface, and the ensuing solvation dynamics of the formed alkali cation, Ak⁺, is followed by ionizing a Xe atom, located in the droplet interior, and recording the yields of Ak⁺He_<i>n</i> ions expelled from the droplet as a function of the pump-probe pulse delay. We found that Li⁺, Na⁺ and K⁺ ions solvate with a binding rate of 1.8 ± 0.1, 1.8 ± 0.1 and 1.7 ± 0.1 He per ps, respectively. Furthermore, by comparing the number distribution of the Ak⁺He_<i>n</i> ion yields with the evaporation energies of these ion-He complexes, obtained by Path Integral Monte Carlo calculations, we identify signatures of the first solvation shells of Li⁺, Na⁺ and K⁺. Lastly, we determine the time-dependent dissipation of the solvation energy from the vicinity of the three alkali ion species and found that the rate is the highest (lowest) for Li⁺ (K⁺).