Theory of heat transfer between adsorbate vibrational degrees of freedom and ultrafast laser heated hot electrons including vibrational intermode coupling is applied to calculate two-pulse correlation, laser fluence dependence and time dependence of lateral hopping of CO molecules from a step to terrace site on a stepped Pt (111) surface. The intermode coupling is a key ingredient to describe vibrational heating of the frustrated translation mode responsible for the CO hopping. The calculated results are in good agreement with the experimental results, especially if we scale down the experimentally determined absorbed fluence. It is found that CO hopping is induced by indirect heating of the FT mode by the FR mode with a strong frictional c...
Ultrafast ime-resolved studies of the vibrational motions of CO on Cu(111) are described. In particu...
The dynamics of lateral manipulation for cobalt/Cu(111) has been investigated combining the model of...
In time-resolved pump-probe vibrational spectroscopy the internal stretch mode of polar molecules is...
We present a theory for the energy transfer between adsorbates and ultrafast laser heated hot electr...
We study the heat transfer from femtosecond laser-heated hot electrons in a metal to adsorbates in t...
We present a theoretical study of the lateral hopping of a single CO molecule on Cu (111) induced by...
Strong short laser pulses can give rise to a strong increase in the electronic temperature at metal ...
The laser-induced movement of CO molecules over a platinum surface was followed in real time by mean...
Carbon monoxide on copper surfaces continues to be a fascinating, rich microlab for many questions e...
Time-resolved vibrational spectroscopy constitutes an invaluable experimental tool for monitoring ho...
The transient response of the internal stretch vibration of CO molecularly adsorbed on Cu ( 111) has...
A Langevin model accounting for all six molecular degrees of freedom is applied to femtosecond-laser...
We report the first study of femtosecond desorption of CO from Pt(111), using 800 nm laser pulses wi...
Fundamental insights into the ultrafast dynamics of energy transfer processes at surfaces are of cen...
The energy transfer between metal substrates and adsorbates occurs on an ultrafast timescale, mediat...
Ultrafast ime-resolved studies of the vibrational motions of CO on Cu(111) are described. In particu...
The dynamics of lateral manipulation for cobalt/Cu(111) has been investigated combining the model of...
In time-resolved pump-probe vibrational spectroscopy the internal stretch mode of polar molecules is...
We present a theory for the energy transfer between adsorbates and ultrafast laser heated hot electr...
We study the heat transfer from femtosecond laser-heated hot electrons in a metal to adsorbates in t...
We present a theoretical study of the lateral hopping of a single CO molecule on Cu (111) induced by...
Strong short laser pulses can give rise to a strong increase in the electronic temperature at metal ...
The laser-induced movement of CO molecules over a platinum surface was followed in real time by mean...
Carbon monoxide on copper surfaces continues to be a fascinating, rich microlab for many questions e...
Time-resolved vibrational spectroscopy constitutes an invaluable experimental tool for monitoring ho...
The transient response of the internal stretch vibration of CO molecularly adsorbed on Cu ( 111) has...
A Langevin model accounting for all six molecular degrees of freedom is applied to femtosecond-laser...
We report the first study of femtosecond desorption of CO from Pt(111), using 800 nm laser pulses wi...
Fundamental insights into the ultrafast dynamics of energy transfer processes at surfaces are of cen...
The energy transfer between metal substrates and adsorbates occurs on an ultrafast timescale, mediat...
Ultrafast ime-resolved studies of the vibrational motions of CO on Cu(111) are described. In particu...
The dynamics of lateral manipulation for cobalt/Cu(111) has been investigated combining the model of...
In time-resolved pump-probe vibrational spectroscopy the internal stretch mode of polar molecules is...