6533b853fe1ef96bd12ad7e5

RESEARCH PRODUCT

Setting the photoelectron clock through molecular alignment

Andrea TrabattoniJoss WieseUmberto De GiovanniniJean-françois OlivieriTerry MullinsJolijn OnvleeSang-kil SonBiagio FrusteriAngel RubioSebastian TrippelJochen Küpper

subject

Chemical Physics (physics.chem-ph)Atomic Physics (physics.atom-ph)ScienceChemical physicsQQuantum physicsFOS: Physical sciencesSettore FIS/03 - Fisica Della MateriaArticlePhysics - Atomic PhysicsStrong field ionizationTDDFTPhysics - Chemical Physicslcsh:QAtomic and molecular physicsddc:500Physics - Atomic and Molecular Clusterslcsh:ScienceAtomic and Molecular Clusters (physics.atm-clus)Applied optics

description

The interaction of strong laser fields with matter intrinsically provides a powerful tool for imaging transient dynamics with an extremely high spatiotemporal resolution. Here, we study strong-field ionisation of laser-aligned molecules, and show a full real-time picture of the photoelectron dynamics in the combined action of the laser field and the molecular interaction. We demonstrate that the molecule has a dramatic impact on the overall strong-field dynamics: it sets the clock for the emission of electrons with a given rescattering kinetic energy. This result represents a benchmark for the seminal statements of molecular-frame strong-field physics and has strong impact on the interpretation of self-diffraction experiments. Furthermore, the resulting encoding of the time-energy relation in molecular-frame photoelectron momentum distributions shows the way of probing the molecular potential in real-time, and accessing a deeper understanding of electron transport during strong-field interactions.

10.1038/s41467-020-16270-0https://hdl.handle.net/21.11116/0000-0001-B02B-821.11116/0000-0006-788A-821.11116/0000-0006-788B-7