Abstract
Processes that break molecular bonds are typically observed with molecules occupying a mixture of quantum states and successfully described with quasiclassical models, while a few studies have explored the distinctly quantum mechanical low-energy regime. Here, we use photodissociation of diatomic strontium molecules to demonstrate the crossover from the ultracold, quantum regime where photofragment angular distributions strongly depend on the kinetic energy to the quasiclassical regime. Using time-of-flight imaging for photodissociation channels with millikelvin reaction barriers, we explore photofragment energies in the 0.1–300 mK range experimentally and up to 3 K theoretically, and discuss the energy scale at which the crossover occurs. We find that the effects of quantum statistics can persist to high photodissociation energies.
- Received 22 May 2018
DOI:https://doi.org/10.1103/PhysRevLett.121.143401
© 2018 American Physical Society
Physics Subject Headings (PhySH)
Synopsis
The Quantum and Classical Sides of a Chemical Reaction
Published 2 October 2018
Experiments track a simple molecule dissociating to find when the reaction can be described with a quantum model and when a semiclassical one will do.
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