Erattupuzha S, Covington CL, Russakoff A, Lotstedt E, Larimian S, Hanus V, Bubin S, Koch M, Gräfe S, Baltuska A, Xie X, Yamanouchi K, Varga K, Kitzler M (2017)
Publication Type: Journal article
Publication year: 2017
Book Volume: 50
Article Number: 125601
Journal Issue: 12
We present the results of a combined experimental and numerical study on strong-field ionisation of acetylene performed with the aim of identifying the mechanism behind the previously reported surprisingly large multi-electron ionisation probabilities of polyatomic molecules. Using coincidence momentum imaging techniques and time-dependent density functional simulations, we show that the reported efficient ionisation is due to the combined action of a significant geometrically induced energy upshift of the most relevant valence orbitals as the C-H distance stretches beyond about two times the equilibrium distance, and a strong increase in the coupling between multiple molecular orbitals concomitant with this stretch motion. The identified enhanced ionisation mechanism, which we refer to as EIC-MOUSE, is only effective for molecules aligned close to parallel to the laser polarisation direction, and is inhibited for perpendicularly aligned molecules because of a suppression of the C-H stretch motion during the onset of ionisation.
APA:
Erattupuzha, S., Covington, C.L., Russakoff, A., Lotstedt, E., Larimian, S., Hanus, V.,... Kitzler, M. (2017). Enhanced ionisation of polyatomic molecules in intense laser pulses is due to energy upshift and field coupling of multiple orbitals. Journal of Physics B-Atomic Molecular and Optical Physics, 50(12). https://doi.org/10.1088/1361-6455/aa7098
MLA:
Erattupuzha, Sonia, et al. "Enhanced ionisation of polyatomic molecules in intense laser pulses is due to energy upshift and field coupling of multiple orbitals." Journal of Physics B-Atomic Molecular and Optical Physics 50.12 (2017).
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