Ultrafast laser-induced desorption of NO and CO molecules on a platinum surface reveals that the rate of energy transfer between the laser-heated electrons and the adsorbate depends critically on the precise adsorbate location. An analysis based on a simple electronic friction model suggests that this femtosecond energy transfer occurs ~3 times faster to adsorbates at step sites compared to adsorbates located on atomically flat surface regions. Density functional theory calculations of vibrational damping rates by electron-hole pair excitations corroborate the increased rate of energy transfer at step sites and show that it is caused primarily by an increased local density of adsorbate-induced states around the Fermi level.

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Persistent URL dx.doi.org/10.1021/jp070470g
Journal J. Phys. Chem. C
Backus, E.H.G, Forsblom, M, Persson, M, & Bonn, M. (2007). Highly efficient ultrafast energy transfer into molecules at surface step sites. J. Phys. Chem. C, 111, 6149–6153. doi:10.1021/jp070470g