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Robust transverse structures in rescattered photoelectron wavepackets and their consequences

2020, Bredtmann, T., Patchkovskii, S.

Initial-state symmetry has been under-appreciated in strong-field spectroscopies, where laser fields dominate the dynamics. We demonstrate numerically that the transverse photoelectron phase structure, arising from the initial-state symmetry, is robust in strong-field rescattering, and has pronounced effects on strong-field photoelectron spectra. Interpretation of rescattering experiments need to take these symmetry effects into account. In turn, robust transverse photoelectron phase structures may enable attosecond sub-Ångström super-resolution imaging with structured electron beams.

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Strong field ionization of small hydrocarbon chains with full 3D momentum analysis

2015, Schulz, Claus Peter, Birkner, Sascha, Furch, Federico J., Anderson, Alexandria, Mikosch, Jochen, Schell, Felix, Vrakking, Marc J. J.

Strong field ionization of small hydrocarbon chains is studied in a kinematic complete experiment using a reaction microscope. By coincidence detection of ions and electrons different ionization continua populated during the ionization process are identified. In addition, photoelectron momentum distributions from laser-aligned molecules allow to characterize the electron wavepackets emerging from different Dyson orbitals.

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NO2molecular frame photoelectron angular distributions for a range of geometries using the R-matrix method

2015, Brambila, Danilo S., Harvey, Alex G., Mašín, Zdeněk, Smirnova, Olga

We present R-matrix calculations of photoionization from NO2, resolved in energy, angle, and both neutral and ionic state, for a range of molecular geometries, including in the vicinity of the 2A1/2B2 conical intersection.

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Mapping the dissociative ionization dynamics of molecular nitrogen with attosecond resolution

2015, Klinker, M., Trabattoni, A., González-Vázquez, J., Liu, C., Sansone, G., Linguerri, R., Hochlaf, M.., Klei, J., Vrakking, M.J.J., Martin, F., Nisoli, M., Calegari, F.

We wish to understand the processes underlying the ionization dynamics of N2 as experimentally induced and studied by recording the kinetic energy release (KER) in a XUV-pump/IR-probe setup. To this end a theoretical model was developed describing the ionization process using Dyson Orbitals and, subsequently, the dissociation process using a large set of diabatic potential energy surfaces (PES) on which to propagate. From said set of PES, a small subset is extracted allowing for the identification of one and two photon processes chiefly responsible for the experimentally observed features.