Disentangling reaction rate acceleration in microdroplets

We have investigated the origin of the unexpected, recently discovered phenomenon of reaction rate acceleration in water microdroplets relative to bulk water. Acceleration factors for reactions of atmospheric and synthetic relevance can be dissected into elementary contributions thanks to the original and versatile kinetic model. The microdroplet is partitioned in two sub-volumes, the surface and the interior, operating as interconnected chemical reactors in the fast diffusion regime. Reaction rate acceleration and its dependence on reaction molecularity and microdroplet dimensions are explained by applying transition-state-theory at thermodynamic equilibrium. We also show that our model, in combination with experimental measurements of rate acceleration factors, can be used to obtain chemical kinetics data at the air-water interface, which has been a long-standing challenge for chemists. The observed rate acceleration of chemical reactions in water microdroplets is elucidated using a simple kinetic model that separates the core and surface contributions, and can be used to determine the rate constants at the air-water interface.