1. Vacuum Ultraviolet Excited State Dynamics of the Smallest Ketone: Acetone
- Author
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Rune Lausten, Ruaridh Forbes, Andrey E. Boguslavskiy, Simon P. Neville, Albert Stolow, Michael S. Schuurman, Anja Röder, and Martin A. B. Larsen
- Subjects
Physics ,Photon ,Valence (chemistry) ,Quantum dynamics ,Molecular physics ,Spectral line ,symbols.namesake ,X-ray photoelectron spectroscopy ,Excited state ,Femtosecond ,Physics::Atomic and Molecular Clusters ,Rydberg formula ,symbols ,General Materials Science ,Physical and Theoretical Chemistry - Abstract
We combined tunable vacuum-ultraviolet time-resolved photoelectron spectroscopy (VUV-TRPES) with high-level quantum dynamics simulations to disentangle multistate Rydberg-valence dynamics in acetone. A femtosecond 8.09 eV pump pulse was tuned to the sharp origin of the A1(n3dyz) band. The ensuing dynamics were tracked with a femtosecond 6.18 eV probe pulse, permitting TRPES of multiple excited Rydberg and valence states. Quantum dynamics simulations reveal coherent multistate Rydberg-valence dynamics, precluding simple kinetic modeling of the TRPES spectrum. Unambiguous assignment of all involved Rydberg states was enabled via the simulation of their photoelectron spectra. The A1(ππ*) state, although strongly participating, is likely undetectable with probe photon energies ≤8 eV and a key intermediate, the A2(nπ*) state, is detected here for the first time. Our dynamics modeling rationalizes the temporal behavior of all photoelectron transients, allowing us to propose a mechanism for VUV-excited dynamics in acetone which confers a key role to the A2(nπ*) state.
- Published
- 2021