M. Weidemüller

We are developing a new hybrid atom-ion trap to study the interaction of ultracold rubidium atoms with mass-selected OH- molecules. The ions are trapped inside an octupole rf-trap made of thin wires instead of the commonly used rods. This ensures good optical access to the center of the trap where the ions can be overlapped with laser cooled rubidium atoms stored in a dark spontaneous force optical trap (dark SPOT). This setup provides high collision rates since the density in a dark SPOT is about one order of magnitude higher than in a standard magneto-optical trap. Further, inelastic collisions with excited atoms are suppressed since almost all atoms are in the ground state. Numerical simulations of our setup using SIMION predict that cooling of the ions is feasible.

We theoretically investigate the dynamics of a trapped ion immersed in a spatially localized buffer gas. For a homogeneous buffer gas, the ion reaches a stable equilibrium only if the mass ratio of the buffer gas atom to the ion is below a critical value. We show how this limitation can be overcome by using multipole traps and a spatially confined buffer gas. Using a generalized model for elastic collisions of the ion with the buffer gas atoms, the ion's energy distribution is derived for arbitrary buffer gas distributions and trap parameters. Three regimes characterized by the analytical form of the ion's energy distribution are found. Final ion temperatures down to the millikelvin regime can be achieved even for heavy buffer gases by actively controlling the size of the buffer gas or the trap voltage (forced sympathetic cooling).

We report on the realisation of a chip-based multipole ion trap manufactured using micro-electromechanical systems (MEMS) technology. It provides ion confinement in an almost field-free volume between two planes of radiofrequency electrodes, deposited on glass substrates, which allows for optical access to the trap. An analytical model of the effective trapping potential is presented and compared with numerical calculations. Stable trapping of argon ions is achieved and a lifetime of 16s is measured. Electrostatic charging of the chip surfaces is studied and found to agree with a numerical estimate.

We identify plain evaporation of ions as the fundamental loss mechanism out of a multipole ion trap. Using thermalized negative Cl- ions we find that the evaporative loss rate is proportional to a Boltzmann factor. This thermodynamic description sheds new light on the dynamics of particles in time-varying confining potentials. It specifically allows us to extract the effective depth of the ion trap as the activation energy for evaporation. As a function of the rf amplitude we find two distinct regimes related to the stability of motion of the trapped ions. For low amplitudes the entire trap allows for stable motion and the trap depth increases with the rf field. For larger rf amplitudes, however, rapid energy transfer from the field to the ion motion can occur at large trap radii, which leads to a reduction of the effective trapping volume. In this regime the trap depth decreases again with increasing rf amplitude. We give an analytical parameterization of the trap depth for various multipole traps that allows predictions of the most favorable trapping conditions.

The absolute photodetachment cross section of OH- anions at a rotational and translational temperature of 170K is determined by measuring the detachment-induced decay rate of the anions in a multipole radio-frequency ion trap. In comparison with previous results, the obtained cross section shows the importance of the initial rotational state distribution. Using a tomography scan of the photodetachment laser through the trapped ion cloud, the derived cross section is model-independent and thus features a small systematic uncertainty. The tomography also yields the column density of the OH- anions in the 22-pole ion trap in good agreement with the expected trapping potential of a large field free region bound by steep potential walls.