4.8 Article

De- and Recoherence of Charge Migration in Ionized Iodoacetylene

Journal

JOURNAL OF PHYSICAL CHEMISTRY LETTERS
Volume 10, Issue 15, Pages 4273-4277

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acs.jpclett.9b01687

Keywords

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Funding

  1. U.S. Department of Energy, Office of Science, Basic Energy Sciences [DE-SC0016007]
  2. NSF Graduate Research Fellowship Program [DGE-1256259]
  3. Robert Draper Technology Innovation Fund [135-AAC6972]
  4. U.S. Department of Energy, Basic Energy Sciences (DOE-BES), Division of Chemical Sciences [DE-FG02-05ER15731]
  5. Office of Science of the U.S. Department of Energy [DE-AC02-05CH11231]
  6. NSF through the University of Wisconsin Materials Research Science and Engineering Center [DMR-1720415]

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During charge migration, electrons flow rapidly from one site of a molecule to another, perhaps inducing subsequent processes (e.g., selective breaking of chemical bonds). The first joint experimental and theoretical preparation and measurement of the initial state and subsequent quantum dynamics simulation of charge migration for fixed nuclei was demonstrated recently for oriented, ionized iodoacetylene. Here, we present new quantum dynamics simulations for the same system with moving nuclei. They reveal the decisive role of the nuclei, i.e. they switch charge migration off (decoherence) and on (recoherence). This is a new finding in attosecond-to-femtosecond chemistry and physics which opens new prospects for laser control over electronic dynamics via nuclear motions.

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