| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5390786 | Chemical Physics Letters | 2008 | 14 Pages |
The advent of attosecond pulsed radiation leads to a large unexplored scientific area in chemical physics: the direct time-resolved measurement of electronic quantum dynamics. Major scientific goals include spectroscopy of single- and multi-electron motion and dynamical electron correlations, relating to orbital interactions in valence and core electronic levels of atoms and molecules. The results of such studies address a wide array of scientific and technological applications. Here, the current state-of-the-art of attosecond-dynamics measurements is reviewed and several novel spectroscopic methods are discussed that are particularly important for applications in chemical physics: attosecond transient absorption/dispersion spectroscopy, laser-induced-dipole spectroscopy, and absolute-phase spectroscopy.
Graphical abstractSimulation of plasmon surface potentials on nanoparticles mapped by attosecond photoelectron spectroscopy, one of several novel attosecond spectroscopy methods described.Download full-size image
