Infrared spectroscopic signature of the structural diversity of the water heptamer

Abstract

As a key species in understanding the hydrogen-bonding network transitions between liquid water and ice, the neutral water heptamer is a challenging experimental target, owing to the richness of low-lying isomers. Here, we report the size-specific infrared spectra of confinement-free, neutral water heptamer (H2O)7 based on threshold photoionization using a tunable vacuum ultraviolet free electron laser. The complexity of the observed spectra indicates that many nearly isoenergetic isomers are present at finite temperatures. Two classes of prism- and cage-like structures are identified in a high-pressure pulsed supersonic expansion of water heptamer, in which the former is favored energetically at low temperatures and serves as a major contributor to the experimental spectrum. These findings provide key information for filling the gap between well-studied water hexamer and octamer.