Abstract
The coupling of (photo)chemical
processes to optical cavity vacuum fields is an emerging method for modulating
molecular and material properties. Recent reports have shown that strong
coupling of the vibrational modes of solvents to cavity vacuum fields can
influence the chemical reaction kinetics of dissolved solutes. This suggests
that vibrational strong coupling might also effect other important solution-based
processes, such as crystallization from solution. Here we test this hither-to
unexplored notion, investigating pseudopolymorphism in the crystallization from
water of ZIF metal-organic frameworks inside optical microcavities. We find
that ZIF-8 crystals are selectively obtained from solution inside optical
microcavities, where the OH stretching vibration of water is strongly coupled
to cavity vacuum fields, whereas mixtures of ZIF-8 and ZIF-L are obtained otherwise.
This work suggests that cavity vacuum fields might become a tool for materials synthesis,
biasing molecular self-assembly and driving macroscopic material outcomes.