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Time-resolved photoelectron diffraction imaging of methanol photodissociation involving molecular hydrogen ejection

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Trinter,  Florian       
Molecular Physics, Fritz Haber Institute, Max Planck Society;

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Citation

Yoshikawa, K., Kanno, M., Xue, H., Kishimoto, N., Goto, S., Ota, F., et al. (2024). Time-resolved photoelectron diffraction imaging of methanol photodissociation involving molecular hydrogen ejection. Physical Chemistry Chemical Physics, 26(38), 25118-25130. doi:10.1039/D4CP01015A.


Cite as: https://hdl.handle.net/21.11116/0000-000F-EB1C-A
Abstract
Imaging ultrafast atomic and molecular hydrogen motion with femtosecond time resolution is a challenge for ultrafast spectroscopy due to the low mass and small scattering cross section of the moving neutral hydrogen atoms and molecules. Here, we propose time- and momentum-resolved photoelectron diffraction (TMR-PED) as a way to overcome limitations of existing methodologies and illustrate its performance using a prototype molecular dissociation process involving the sequential ejection of a neutral hydrogen molecule and a proton from the methanol dication. By combining state-of-the-art molecular dynamics and electron-scattering methods, we show that TMR-PED allows for direct imaging of hydrogen atoms in action. More specifically, the fingerprint of hydrogen dynamics reflects the time evolution of polarization-averaged molecular-frame photoelectron angular distributions (PA-MFPADs) as would be recorded in X-ray pump/X-ray probe experiments with few-femtosecond resolution. We present the results of two precursor experiments that support the feasibility of this approach.