English
 
Help Privacy Policy Disclaimer
  Advanced SearchBrowse

Item

ITEM ACTIONSEXPORT

Released

Journal Article

Ultrafast electron dynamics at water covered alkali adatoms adsorbed on Cu(111)

MPS-Authors
/persons/resource/persons21877

Meyer,  Michael
Fachbereich Physik, Freie Universität Berlin;
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

/persons/resource/persons22250

Wolf,  Martin
Fachbereich Physik, Freie Universität Berlin;
Physical Chemistry, Fritz Haber Institute, Max Planck Society;

External Resource
No external resources are shared
Fulltext (restricted access)
There are currently no full texts shared for your IP range.
Fulltext (public)

c4cp05356g.pdf
(Publisher version), 3MB

Supplementary Material (public)
There is no public supplementary material available
Citation

Meyer, M., Agarwal, I., Wolf, M., & Bovensiepen, U. (2015). Ultrafast electron dynamics at water covered alkali adatoms adsorbed on Cu(111). Physical Chemistry Chemical Physics, 17(13), 8441-8448. doi:10.1039/C4CP05356G.


Cite as: https://hdl.handle.net/11858/00-001M-0000-0024-BC31-2
Abstract
Here we report on the ultrafast electron dynamics of the alkalis Na, K, and Cs coadsorbed with D2O on Cu(111) surfaces, which we investigated with femtosecond time-resolved two-photon photoemission. The well known transient electronic binding energy stabilization in bare adsorbed alkalis is enhanced by the presence of water which acts as a solvent and increases the transient energy gain. We observe for all adsorbed alkalis a transient binding energy stabilization of 100–300 meV. The stabilization rates range from 1 to 2 eV ps-1. Here the heavier alkali exhibits a slower stabilization which we explain by their weaker static alkali–water interaction observed in thermal desorption spectroscopy. The population dynamics at low water coverage is described by a single exponential. With increasing water coverage the behavior becomes non-exponential suggesting an additional excited state due to electron solvation