Direct observation of coherence transfer and rotational-to-vibrational energy exchange in optically centrifuged CO<sub>2</sub> super-rotors.
basic_science · Level V
Where this comes from
- Record sourced from PubMed, PMID 37270647.
- Also identified by DOI 10.1038/s41467-023-38873-z and PMC identifier 10239519.
- Licence recorded as CC BY.
- The licence permits redistribution, so the abstract is shown in full and the full text is available from the publisher.
Abstract
Optical centrifuges are laser-based molecular traps that can rotationally accelerate molecules to energies rivalling or exceeding molecular bond energies. Here we report time and frequency-resolved ultrafast coherent Raman measurements of optically centrifuged CO<sub>2</sub> at 380 Torr spun to energies beyond its bond dissociation energy of 5.5 eV (J<sub>max</sub> = 364, E<sub>rot</sub> = 6.14 eV, E<sub>rot</sub>/k<sub>B</sub> = 71, 200 K). The entire rotational ladder from J = 24 to J = 364 was resolved simultaneously which enabled a more accurate measurement of the centrifugal distortion constants for CO<sub>2</sub>. Remarkably, coherence transfer was directly observed, and time-resolved, during the field-free relaxation of the trap as rotational energy flowed into bending-mode vibrational excitation. Vibrationally excited CO<sub>2</sub> (ν<sub>2</sub> > 3) was observed in the time-resolved spectra to populate after 3 mean collision times as a result of rotational-to-vibrational (R-V) energy transfer. Trajectory simulations show an optimal range of J for R-V energy transfer. Dephasing rates for molecules rotating up to 5.5 times during one collision were quantified. Very slow decays of the vibrational hot band rotational coherences suggest that they are sustained by coherence transfer and line mixing.