Abstract
For over a century, termolecular (third-order) chemical reactions have been explained by the Lindemann–Hinshelwood mechanism, assuming sequential stabilization via bimolecular encounters. Here, we demonstrate that barrierless termolecular reactions are fundamentally governed by direct three-body dynamics. Using classical trajectory calculations in hyperspherical coordinates, we quantitatively reproduce ion-atom recombination kinetics across a wide temperature range without invoking intermediate complexes or steady-state assumptions. Our results not only resolve longstanding discrepancies between theory and experiment, but also establish a general mechanistic framework for barrierless termolecular reactions, with implications spanning atmospheric chemistry, plasma physics, and ultracold chemistry.
Funding Information
  • Directorate for Engineering (PHY-2440808)

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