Journal Article PUBDB-2020-04146

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Time-resolving the UV-initiated photodissociation dynamics of OCS

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2020
Soc. Cambridge [u.a.]

Faraday discussions 228, 413 - 431 () [10.1039/D0FD00119H]
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Abstract: We present a time-resolved study of the photodissociation dynamics of OCS after UV- photoexcitation at λ = 237 nm. OCS molecules (X 1Σ+) were primarily excited to the 1 1A′′ and the 2 1A′ Renner-Teller components of the 1Σ− and 1∆ states. Dissociation into CO and S fragments was observed through time-delayed strong-field ionisation and imaging of the kinetic energy of the resulting CO+ and S+ fragments by intense 790 nm laser pulses. Surprisingly, fast oscillations with a period of ∼100 fs were observed in the S+ channel of the UV dissociation. Based on wavepacket-dynamics simulations coupled with a simple electrostatic-interaction model, these oscillations do not correspond to the known highly-excited rotational motion of the leaving CO(X 1Σ+, J ≫ 0) fragments, which has a timescale of ∼140 fs. Instead, we suggest to assign the observed oscillations to the excitation of vibrational wavepackets in the 2 3A′′ or 2 1A′′ states of the molecule that predissociate to form S(3PJ ) photoproducts.

Classification:

Note: 25 pages, 5 figures

Contributing Institute(s):
  1. FS-CFEL-3 (CFEL-DESYT)
  2. CFEL-Theory (FS-CFEL-3)
  3. FS-CFEL-1 (Group Leader: Henry Chapman) (CFEL-I)
  4. CFEL-CMI (FS-CFEL-CMI)
  5. Uni Hamburg / Experimentalphysik (UNI/EXP)
Research Program(s):
  1. 6211 - Extreme States of Matter: From Cold Ions to Hot Plasmas (POF3-621) (POF3-621)
  2. AIM - CUI: Advanced Imaging of Matter (390715994) (390715994)
Experiment(s):
  1. No specific instrument

Appears in the scientific report 2020
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Time-resolving the UV-initiated photodissociation dynamics of OCS
1-25 () [10.3204/PUBDB-2021-02517]  GO OpenAccess  Download fulltext Files  Download fulltextFulltext by arXiv.org BibTeX | EndNote: XML, Text | RIS


 Record created 2020-11-02, last modified 2025-07-16