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The electron emission pattern of transfer-ionization in collisions of He$^{2+}$ with He was investigated for impact velocities between 0.53 a.u. and 0.77 a.u. (7 keV/u - 15 keV/u) employing recoil-ion momentum spectroscopy. This process is known to be dominated by the promotion of the 2p$\pi$ molecular orbital into the continuum which results in "banana" shaped areas of high electron momentum densities extending from the target to the projectile in velocity space in the collision plain. Asymmetries are explained by a coherent superposition of the 2p$\pi$ channel of the quasi molecular promotion with the 1s$\sigma$ channel. Here we report on an additional contribution of higher angular momentum molecular states for close collisions which emerge at smaller impact velocities. They show up as highly structured electron emission patterns in the plane perpendicular to the direction of impact.

Using the cold target recoil ion momentum spectroscopy (COLTRIMS) technique, we have measured the simultaneous projectile and target ionization in collisions of He$^+$ projectiles with a mixture of gaseous H$_2$ and D$_2$ for an incident projectile energy of 650 keV. Motivated by Cooper et al. [Phys. Rev. Lett. 100, 043204 (2008)], we look for differences in the ionization cross section of the two isotopes with the highest resolution and statistical significance. Contributions of the electron-electron and electron-nucleus interactions have been clearly separated kinematically by measuring the longitudinal and transverse momentum of the recoiling ion. We find no significant isotope effect in any of our momentum distributions., Comment: 13 pages, 6 figures

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., Comment: 6 pages, 4 figures

We have measured the molecular frame angular distributions of photoelectrons emitted from the Carbon K shell of fixed-in-space CO molecules for the case of simultaneous excitation of the remaining molecular ion. Normal and conjugate shake up states are observed. Photo electrons belonging to normal \Sigma -satellite lines show an angular distribution resembling that observed for the main photoline at the same electron energy. Surprisingly a similar shape is found for conjugate shake up states with \Pi -symmetry. In our data we identify shake rather than electron scattering (PEVE) as the mechanism producing the conjugate lines. The angular distributions clearly show the presence of a \Sigma -shape resonance for all of the satellite lines., Comment: 8 pages, 2 figures

Results of the most sophisticated measurements in coincidence of the angular resolved K-shell photo- and Auger-electrons, and of two atomic ions produced by dissociation of N2 molecule, are analyzed. Detection of photoelectrons at certain angles allows separating the Auger decay processes of the 1{\sigma}g and 1{\sigma}u core hole states. The Auger electron angular distributions for each of these hole states are measured as a function of the kinetic energy release of two atomic ions and are compared with the corresponding theoretical angular distributions. From that comparison one can disentangle the contributions of different repulsive doubly charged molecular ion states to the Auger decay. Different kinetic energy release values are directly related to the different internuclear distances. In this way one can trace experimentally the behavior of the potential energy curves of dicationic final states inside the Frank-Condon region. Presentation of the Auger electron angular distributions as a function of kinetic energy release of two atomic ions opens a new dimension in the study of Auger decay.

We investigate photo-double-ionization of H2 by circular polarized photons at hν=160eV. The previously observed two-center interference pattern in the angular distribution of the electron sum momentum is shown to depend strongly on the internuclear distance and the summed electron momenta.

Using the COLTRIMStechnique, scattering angle differential cross sections for single and double electron capture in collisions of protons and $He\sp{1,2+}$ 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.

Time ordering may be defined by first defining the limit of no time ordering (NTO) in terms of a time average of an external interaction, V(t). Previously, time correlation was defined in terms of a similar limit called the independent time approximation (ITA). Experimental evidence for time correlation has not yet been distinguished from experimental evidence for time ordering.

A small electrostatic storage ring is the central machine of the Frankfurt Ion stoRage Experiments (FIRE) which will be built up at the new Stern-Gerlach-Center of Frankfurt University. With ion energies up to 50 keV it enables the analysis of complex many-particle systems from atoms to very large bio molecules. The high luminosity of the beam allows measurements with many orders of magnitude better resolution compared to traditional measurements. It will be combined with existing experiments, like the reaction microscope COLTRIMS and the ECR ion source. In comparison to earlier designs, the ring lattice was modified in many details: Problems in earlier designs were related with e.g. the detection of light particles and highly charged ions with different charge states. Therefore, the deflectors were redesigned completely, allowing a more flexible positioning of the diagnostic elements. In this contribution, the final design of the storage ring is presented and the layout of all elements given.