1. All-XUV Pump-Probe Transient Absorption Spectroscopy of the Structural Molecular Dynamics of Di-iodomethane
- Author
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Rebholz, M, Ding, T, Despré, V, Aufleger, L, Hartmann, M, Meyer, K, Stooß, V, Magunia, A, Wachs, D, Birk, P, Mi, Y, Borisova, GD, Castanheira, CDC, Rupprecht, P, Schmid, G, Schnorr, K, Schröter, CD, Moshammer, R, Loh, ZH, Attar, AR, Leone, SR, Gaumnitz, T, Wörner, HJ, Roling, S, Butz, M, Zacharias, H, Düsterer, S, Treusch, R, Brenner, G, Vester, J, Kuleff, AI, Ott, C, and Pfeifer, T
- Subjects
Astronomical and Space Sciences ,Condensed Matter Physics ,Quantum Physics - Abstract
In this work, we use an extreme-ultraviolet (XUV) free-electron laser (FEL) to resonantly excite the I: 4d5/2-σ∗ transition of a gas-phase di-iodomethane (CH2I2) target. This site-specific excitation generates a 4d core hole located at an iodine site, which leaves the molecule in a well-defined excited state. We subsequently measure the time-dependent absorption change of the molecule with the FEL probe spectrum centered on the same I: 4d resonance. Using ab initio calculations of absorption spectra of a transient isomerization pathway observed in earlier studies, our time-resolved measurements allow us to assign the timescales of the previously reported direct and indirect dissociation pathways. The presented method is thus sensitive to excited-state molecular geometries in a time-resolved manner, following a core-resonant site-specific trigger.
- Published
- 2021