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  Can we control lifetimes of electronic states at surfaces by adsorbate resonances?

Hotzel, A., Ishioka, K., Knoesel, E., Wolf, M., & Ertl, G. (1998). Can we control lifetimes of electronic states at surfaces by adsorbate resonances? Chemical Physics Letters, 285(3-4), 271-277. doi:10.1016/S0009-2614(98)00054-2.

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 Creators:
Hotzel, Arthur1, Author           
Ishioka, Kunie2, Author
Knoesel, Ernst1, Author           
Wolf, Martin1, Author
Ertl, Gerhard1, Author           
Affiliations:
1Physical Chemistry, Fritz Haber Institute, Max Planck Society, ou_634546              
2National Research Institute for Metals, 1-2-1 Sengen, Tsukuba, Ibaraki 305, Japan, ou_persistent22              

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 Abstract: Femtosecond time-resolved two-photon photoemission is used to study the excited electronic states of a Cu(111) surface covered with a monolayer of physisorbed O2 on top of one to five Xe spacer layers. The spectra are dominated by a state 4.0 eV above EF whose lifetime depends strongly on the number of Xe spacer layers. The lifetime decreases with increasing number of spacer layers from (650±30) fs for one Xe layer to (90±10) fs for five layers. To explain this trend we propose a model where the image potential states couple to a negative-ion resonance of the O2 molecule.

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Language(s): eng - English
 Dates: 1997-12-301997-09-291997-12-301998-03-20
 Publication Status: Issued
 Pages: 7
 Publishing info: -
 Table of Contents: -
 Rev. Type: Peer
 Identifiers: DOI: 10.1016/S0009-2614(98)00054-2
 Degree: -

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Title: Chemical Physics Letters
  Other : Chem. Phys. Lett.
Source Genre: Journal
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Publ. Info: Amsterdam : North-Holland
Pages: 7 Volume / Issue: 285 (3-4) Sequence Number: - Start / End Page: 271 - 277 Identifier: ISSN: 0009-2614
CoNE: https://pure.mpg.de/cone/journals/resource/954925389241