Journal
NATURE CHEMISTRY
Volume 13, Issue 1, Pages 70-+Publisher
NATURE RESEARCH
DOI: 10.1038/s41557-020-00607-9
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Funding
- Division of Chemical Sciences, Geosciences and Biosciences, Office of Basic Energy Sciences, of the US Department of Energy [DE-SC0015429]
- NSF [DGE-1656466]
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Research has shown that controlling molecular vibrations can accelerate certain electron transfer reactions and determine the process in which vibrations participate in the reaction. Experiments have observed ballistic electron transfer along a reaction coordinate with high-frequency promoting vibrations, as well as the system becoming impulsively out of equilibrium due to the electron transfer reaction.
Electron transfer reactions facilitate energy transduction and photoredox processes in biology and chemistry. Recent findings show that molecular vibrations can enable the dramatic acceleration of some electron transfer reactions, and control it by suppressing and enhancing reaction paths. Here, we report ultrafast spectroscopy experiments and quantum dynamics simulations that resolve how quantum vibrations participate in an electron transfer reaction. We observe ballistic electron transfer (similar to 30 fs) along a reaction coordinate comprising high-frequency promoting vibrations. Along another vibrational coordinate, the system becomes impulsively out of equilibrium as a result of the electron transfer reaction. This leads to the generation (by the electron transfer reaction, not the laser pulse) of a new vibrational coherence along this second reaction coordinate in a mode associated with the reaction product. These results resolve a complex reaction trajectory composed of multiple vibrational coordinates that, like a sequence of ratchets, progressively diminish the recurrence of the reactant state.
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