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Christian A. Schröder

Publications and source records attributed to Christian A. Schröder.

3 recordsLinked to original sources

Coherent vibrational dynamics in molecular bond breaking: methyl radical umbrella mode probed by femtosecond x-ray spectroscopy

We report on the observation of coherent molecular vibrations launched by the breaking of a molecular bond. The methyl radical, which is produced by $267\,\mathrm{nm}$ photodissociation of methyl iodide, is excited to high levels in its $ν_2$ ``umbrella" vibrational mode by the dissociation. The ensuing coherent vibrational dynamics are observed by measuring ultrafast time-dependent changes in the x-ray transition energy from the C$1s$ to the singly-occupied valence orbital. Due to symmetry, the real space vibrational motion appears predominantly in the x-ray energy shift at the difference frequencies of the $ν_2$ progression, although the fundamental frequencies of the $ν_2$ mode are also observed. By constructing a fully quantum-mechanical model of the dynamics the coherent superposition is rigorously characterized and the real-space motion of the radicals is reconstructed. The retrieved trajectories are dominated by pronounced quantum beating governed by the high degree of coherent excitation and the strong negative anharmonicity of the $ν_2$ mode.

physics.atom-ph↗

Photoemission Chronoscopy of the Iodoalkanes

Time delays in photoemission are on the order of attoseconds and have been experimentally determined in atoms, molecules and solids. Their magnitude and energy dependence are expected to yield fundamental insights into the properties of the systems in which they're measured. In a recent study Biswas \textsl{et al.} (Biswas, S., Förg, B., Ortmann, L. et al. Probing molecular environment through photoemission delays. Nat. Phys. 16, 778-783 (2020)) determined the absolute photoemission time of the I$4d$ level in iodoethane via attosecond streaking spectroscopy, finding the presence of a functional group to increase the photoemission time delay, suggesting a correlation between the size of the functional group and time delay based on a semi-classical calculation. Here we experimentally study the dependence of the I$4d$ photoemission time on the functional group in the iodoalkanes from iodomethane up to 2-iodobutane at three photon energies across the giant resonance in the I$4d\to\varepsilon f$ photoemission channel, finding that the presence alone of a functional group does not necessarily increase the photoemission delay, and that overall no clear correlation between its size and the photoemission time delay can be established.

physics.chem-ph↗

Versatile, open-source program for simulating high-harmonic generation

Light sources based on high-harmonic generation (HHG) underpin ultrafast spectroscopy experiments across a large range of photon energies, spanning from the extreme-ultraviolet to the soft x-ray. To this day their design, implementation and improvement presents uniqe challenges, but can be aided by numerical tools. Here we present a new simulation program designed for this purpose, which accurately takes both macroscopic and microscopic aspects of high-harmonic generation into account and is therefore applicable across the broad range of parameters that HHG based light sources are today utilized in. The program is validated by calculating harmonic emission in four common experimental configurations.

physics.optics↗