Abstract
Tracking electron motion in molecules is the key to understanding and controlling chemical transformations. Contemporary techniques in attosecond science are able to generate and trace the consequences of this motion in real time, but not in real space. Scanning tunnelling microscopy, on the other hand, can locally probe the valence electron density in molecules, but cannot alone provide dynamical information at this ultrafast timescale. Here we show that, by combining scanning tunnelling microscopy and attosecond technologies, quantum electronic coherences induced in molecules by <6-fs-long carrier-envelope-phase-stable near-infrared laser pulses can be directly visualized at ångström-scale spatial and subfemtosecond temporal resolutions. We demonstrate concurrent real-space and -time imaging of coherences involving the valence orbitals of perylenetetracarboxylic dianhydride molecules, and full control over the population of the involved orbitals. This approach opens the way to the unambiguous observation and manipulation of electron dynamics in complex molecular systems.
Highlights
Tracking electron motion in molecules is the key to understanding and controlling chemical transformations
Chemical transformations in molecules are a consequence of valence electron motion and its eventual coupling to nuclear motion[1,2,3,4]
The local time-evolution of the electron density can only be inferred by reconstruction from the features appearing in electron, ion, absorption or emission spectra[9,10,11,12]
Summary
Tracking electron motion in molecules is the key to understanding and controlling chemical transformations. When the HOMO of the PTCDA molecules is aligned with the Fermi level of the tungsten nanotip, the laser-driven tunnelling current images the spatial profile of the HOMO orbitals (Fig. 2d).
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