- Iskandar, W;
- Gatton, AS;
- Gaire, B;
- Sturm, FP;
- Larsen, KA;
- Champenois, EG;
- Shivaram, N;
- Moradmand, A;
- Williams, JB;
- Berry, B;
- Severt, T;
- Ben-Itzhak, I;
- Metz, D;
- Sann, H;
- Weller, M;
- Schoeffler, M;
- Jahnke, T;
- Dörner, R;
- Slaughter, D;
- Weber, Th
We have conducted an experimental study on the photo double ionization (PDI) of carbon-dioxide dimers at photon energies of 37 and 55 eV and oxygen dimers at photon energies of 38, 41.5, and 46 eV, while focusing on the dissociation dynamics upon single-photon absorption. The investigation was performed by applying the cold-target recoil-ion momentum spectroscopy method in order to collect and record the three-dimensional momenta of the ionic fragments and emitted electrons from the dissociating dimer in coincidence. The kinetic-energy release upon fragmentation and the electron angular distributions in the laboratory and body-fixed frames, as well as the relative electron-electron emission angle, show unambiguous experimental evidence of intermolecular Coulombic decay (ICD) in carbon-dioxide dimers upon photoionization below and above the double-ionization threshold of CO2 monomers. The PDI of oxygen dimers is less conclusive and shows contributions from ICD and knock-off ionization mechanisms. As for atomic dimers, the present results reveal that ICD in CO2 dimers after valence PDI can also serve as a source for low-energy electrons, known to be very relevant in biological systems, cells, and tissues.