Extracting conformational structure information of benzene molecules via laser-induced electron diffraction.

We have measured the angular distributions of high energy photoelectrons of benzene molecules generated by intense infrared femtosecond laser pulses. These electrons arise from the elastic collisions between the benzene ions with the previously tunnel-ionized electrons that have been driven back by the laser field. Theory shows that laser-free elastic differential cross sections (DCSs) can be extracted from these photoelectrons, and the DCS can be used to retrieve the bond lengths of gas-phase molecules similar to the conventional electron diffraction method.

Extracting electron-ion differential scattering cross sections for partially aligned molecules by laser-induced rescattering photoelectron spectroscopy.

We extract large-angle elastic differential cross sections (DCSs) for electrons scattering from partially aligned O2+ and CO2+ molecules using rescattering photoelectrons generated by infrared laser pulses. The extracted DCSs are in good agreement with those calculated theoretically, demonstrating that accurate DCSs for electron-ion scattering can be extracted from the laser-induced rescattering spectra, thus paving the way for dynamic imaging of chemical reactions by rescattering photoelectron spectroscopy.

Ion-ion coincidence studies on multiple ionizations of N(2) and O(2) molecules irradiated by extreme ultraviolet free-electron laser pulses.

We have investigated multiple ionization of N(2) and O(2) molecules by 52 nm extreme-ultraviolet light pulses at the free-electron laser facility SCSS in Japan. Coulomb break-up of parent ions with charge states up to 5+ is found by the ion-ion coincidence technique. The charge-state dependence of kinetic energy release distributions suggests that the electrons are emitted sequentially in competition with the elongation of the bond length.

Two-source double-slit interference in angle-resolved high-energy above-threshold ionization spectra of diatoms.

When an electron from a diatomic molecule undergoes tunneling-rescattering ionization, a novel form of destructive interference can be realized that involves all four geometric orbits that are available to the electron when it is freed, because both ionization and rescattering may take place at the same or at different centers. We find experimentally and confirm theoretically that in orientation-averaged angle-resolved high-order above-threshold ionization spectra the corresponding destructive interference is visible for O_{2} but not for N_{2}. This effect is different from the suppression of ionization that is well known to occur for O_{2}.