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Open AccessArticle

Ultrafast Vibrational Dynamics of CO Ligands on RuTPP/Cu(110) under Photodesorption Conditions

Surface Science Research Centre and Department of Chemistry, University of Liverpool, Liverpool L69 3BX, UK
Surface and Interface Science Laboratory, RIKEN, Wako, Saitama 351-0198, Japan
Author to whom correspondence should be addressed.
Surfaces 2019, 2(1), 117-130;
Received: 16 December 2018 / Revised: 21 January 2019 / Accepted: 3 February 2019 / Published: 7 February 2019
We have studied CO coordinated to ruthenium tetraphenylporphyrin (RuTPP)/Cu(110) and directly adsorbed to Cu(110), using femtosecond pump-sum frequency probe spectroscopy, to alter the degree of electron-vibration coupling between the metal substrate and CO. We observe the facile femtosecond laser-induced desorption of CO from RuTPP/Cu(110), but not from Cu(110). A change in the vibrational transients, in the first few picoseconds, from a red- to blue-shift of the C–O stretching vibration under photodesorption conditions, was also observed. This drastic change can be explained, if the cause of the C–O frequency redshift of Cu(110) is not the usually-assumed anharmonic coupling to low frequency vibrational modes, but a charge transfer from hot electrons to the CO 2π* state. This antibonding state shifts to higher energies on RuTPP, removing the C–O redshift and, instead, reveals a blueshift, predicted to arise from electron-mediated coupling between the coherently excited internal stretch and low frequency modes in the system. View Full-Text
Keywords: adsorbate dynamics; pump-probe spectroscopy adsorbate dynamics; pump-probe spectroscopy
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MDPI and ACS Style

Omiya, T.; Kim, Y.; Raval, R.; Arnolds, H. Ultrafast Vibrational Dynamics of CO Ligands on RuTPP/Cu(110) under Photodesorption Conditions. Surfaces 2019, 2, 117-130.

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