2025/10/14 by Jeppe K. Christensen, Simon H. Albrechtsen, Christensen, Jeppe K. +17
Chemistry · Physics and Astronomy · #Advanced NMR Techniques and Applications #Chemical Physics (physics.chem-ph) #FOS: Physical sciences #Quantum, superfluid, helium dynamics #Spectroscopy and Quantum Chemical Studies
paper · pdf · doi:10.48550/arxiv.2510.12330
openalex publication_date 2025/10/14 · openalex created_date 2025/10/17 · openalex updated_date 2026/07/28
In 2023, ultrafast pump-probe spectrocopy 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 et al., Nature, 2023, 623, 319]. Subsequently, theoretical studies showed that other alkali ions solvate in a similar manner but no experimental results were 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+Hen ions expelled from the droplet as a function of the pump-probe pulse delay. We find 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+Hen ion yields to 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 find that the rate is highest (lowest) for Li+ (K+)