ABSTRACT
The momentum distribution of photoelectrons in H2+ molecules subjected to an attosecond pulse is theoretically investigated. To better understand the laser-molecule interaction, we develop an in-line photoelectron holography approach that is analogous to optical holography. This approach is specifically suitable for extracting the amplitude and phase of the forward-scattered electron wave packet in a dissociating molecule with atomic precision. We also extend this approach to imaging the transient scattering cross-section of a molecule dressed by a near infrared laser field. This attosecond photoelectron holography sheds light on structural microscopy of dissociating molecules with high spatial-temporal resolution.
ABSTRACT
An analytic description for the yield, P(p), of high-energy electrons ionized from an atom by a short (few-cycle) laser pulse is obtained quantum mechanically. Factorization of P(p) in terms of an electron wave packet and the cross section for elastic electron scattering (EES) is shown to occur only for an ultrashort pulse, while in general P(p) involves interference of EES amplitudes with laser-field-dependent momenta. The analytic predictions agree well with accurate numerical results.
