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Probing electron transfer dynamics at MgO surfaces by Mg-atom desorption.
Alan G Joly1, Matthias Henyk, Kenneth M Beck
1Pacific Northwest National Laboratory, P.O. Box 999, Richland, WA 99352, USA.
The Journal of Physical Chemistry. B
|September 15, 2006
Summary
Ultrafast ultraviolet pulses cause magnesium atom desorption from MgO films. Different ultrafast dynamical paths, including electron transitions and trapping, explain the observed hyperthermal kinetic energies.
Area of Science:
- Surface science
- Materials science
- Physical chemistry
Background:
- High surface area magnesium oxide (MgO) films are technologically relevant.
- Ultraviolet (UV) excitation is a known method for inducing desorption from surfaces.
- Understanding desorption dynamics is crucial for controlling surface reactions and material properties.
Purpose of the Study:
- To investigate the mechanisms of neutral Mg-atom desorption from MgO films induced by femtosecond UV pulses.
- To elucidate the role of electronic and dynamical processes in hyperthermal desorption.
- To compare femtosecond and nanosecond excitation dynamics.
Main Methods:
- High surface area MgO films were prepared.
- Femtosecond UV pulses (4.7 eV) were used for excitation.
- Time-resolved measurements, including two-pulse correlation, were employed to study desorption dynamics.
Main Results:
- Neutral Mg atoms were desorbed with hyperthermal kinetic energies (0.1-0.4 eV).
- Desorption energy and power dependence were similar to nanosecond excitation.
- Femtosecond two-pulse correlation revealed distinct dynamical paths with sub-150 fs and picosecond time scales.
Conclusions:
- Femtosecond UV excitation induces Mg-atom desorption via multiple dynamical pathways.
- A fast mechanism involves simultaneous two-electron transitions to a 3-coordinated Mg(2+) site.
- Slower mechanisms are linked to electron trapping dynamics at surface sites.

