Probing the tunneling site of electrons in strong field enhanced ionization of molecules

Molecules show a much increased multiple ionization rate in a strong laser field as compared to atoms of similar ionization energy. A widely accepted model attributes this to the action of the joint fields of the adjacent ionic core and the laser on its neighbor inside the same molecule. The underlying physical picture for the enhanced ionization is that the up-field atom that gets ionized. However, this is still debated and remains unproven. Here we report an experimental verification of this long-standing prediction. This is accomplished by probing the two-site double ionization of ArXe, where the instantaneous field direction at the moment of electron release and the emission direction of the correlated ionizing center are measured by detecting the recoil sum- and relative-momenta of the fragment ions. Our results unambiguously prove the intuitive picture of the enhanced multielectron dissociative ionization of molecules and clarify a long-standing controversy.

Multiorbital tunneling ionization of the CO molecule

We coincidently measure the molecular frame photoelectron angular distribution and the ion sum-momentum distribution of single and double ionization of CO molecules by using circularly and elliptically polarized femtosecond laser pulses, respectively. The orientation dependent ionization rates for various kinetic energy releases allow us to individually identify the ionizations of multiple orbitals, ranging from the highest occupied to the next two lower-lying molecular orbitals for various channels observed in our experiments. Not only the emission of a single electron, but also the sequential tunneling dynamics of two electrons from multiple orbitals are traced step by step. Our results confirm that the shape of the ionizing orbitals determine the strong laser field tunneling ionization in the CO molecule, whereas the linear Stark effect plays a minor role.

Spatial imaging of the {H_2}^+ vibrational wave function at the quantum limit

We experimentally obtained a direct image of the nuclear wave functions of {H_2}^+ by dissociating the molecule via electron attachment and determining the vibrational state using the COLTRIMS technique. Our experiment visualizes the nodal structure of different vibrational states. We compare our results to the widely used reflection approximation and to quantum simulations and discuss the limits of position measurements in molecules imposed by the uncertainty principle.

State selective differential cross sections for single and double electron capture in $Hesp{1,2+}-He$ and $p-He$ collisons

Using the COLTRIMStechnique, scattering angle differential cross sections for single and double electron capture in collisions of protons and $Hesp{1,2+}$ projectiles with helium atoms for incident energies of $60-630 keV/u$ are measured. We also report new theoretical results obtained by means of four-body one-channel distorted wave models (CDW-BFS, CDW-BIS and BDW), and find mixed agreement with the measured data.