Abstract We simulated the motion of BaH + molecular ions which are sympathetically cooled by laser-cooled Ba + ions in linear quadrupole and octupole radiofrequency (RF) ion traps. By varying the trap voltages, we studied the velocity distribution of hydrogen atoms that would be produced upon threshold photodissociation of the BaH + . We found that hydrogen with a kinetic energy below 30 mK × k B can be produced in both traps, making the scheme suitable for loading hybrid ion–atom traps such as those used to synthesize and trap antihydrogen or study ultracold atom–ion collisions. We discuss how the dynamics of RF traps could be exploited to produce hydrogen below this limit by either driving the photodissociation transition with a small laser beam aligned along the axis of the trap, or by pulsing the laser during the micromotion turning points.
This dissertation details of the construction of and experiments performed in a hybrid system consisting of a cold neutral atomic magneto-optical trap (MOT) contained within a linear radio-frequency quadrupole ion trap (LQT). The combination of these two workhorses of atomic physics facilitates a variety of developing science such as the controlled investigation of ion-neutral quantum chemistry and the production of ground-state molecular ions. While the primary focus of this work is the production of ultracold molecular ions via sympathetic cooling, there has been investigation of cold (T ~ mK) ion-neutral charge exchange processes in two different ion-neutral pair systems. In addition, a possible method of producing ultracold homonuclear molecular ions via a photo-associative ionization (PAI) pathway is studied in the MOT. The LQT traps ions in spatial overlap with a 40Ca MOT constituting an ultracold buffer gas purposed to sympathetically cool molecular ions.An effective, general method of producing ground-state molecular ions would open a field of physics allowing, for example, precise measurements of molecular transitions which are uniquely sensitive to parity violation, or the possible variation of fundamental constants. Another promising application of cold molecular ions is an implementation of a quantum computing architecture by coupling micro-fabricated strip-line resonators to the microwave rotational transition found in many diatomic molecular ions. The molecular ion BaCl+ is chosen to be used in proof-of-principle sympathetic cooling experiments. Ultimately, a vibrational internal state thermometry experiment shows that the Ca MOT performs very efficiently at quenching the vibrational motion of the BaCl+ molecular ion.As a product of overcoming experimental challenges, this thesis discusses several experiments to characterize trapping and reaction dynamics in the hybrid system. For example, charge transfer measurements are performed with two different laser-cooled atomic ion species, Yb+ and Ba+, which are allowed and disallowed ground-state reaction, respectively. Controlled measurements of these inelastic processes test the cutting edge of quantum theory of ion-neutral interaction in both the ground-state and under optical excitation.
The study of ion-molecule reactions plays a vital role in cold chemistry, thus implying the need of well-controlled ion ensembles in a cold environment. The internal and external degrees of freedom of molecular ions, trapped in multipole radio frequency ion traps, can be cooled via collisions with neutral atoms [1]. Usually the coolant undergoes collisions with a thermal shield mounted on a cryostat attaining temperatures of about 4 K. To overcome this lower temperature limit two approaches have been proposed. Firstly, using a laser-cooled buffer-gas localized at the center of the ion cloud [2]. Secondly, sympathetic cooling via a second laser cooled molecular anion like C
2− [3]. This, in addition to its potential role in forming carbon chain anions in the interstellar medium, makes C
2− an important molecule in anion research. In this contribution we present a newly developed 16-pole cryogenic radio frequency wire trap for spectroscopic and kinetic studies of molecular anions. First results of quenching rates of the first excited vibrational level of C
2− due to collisions with H
2 are presented. Furthermore, possible reaction pathways with H
2 are discussed and recent spectroscopic measurements of the second electronic excited state of C
2− are presented. References: [1] R. Wester , J. Phys. B 42, 154001 (2009) [2] B. Höltkemeier et al., Phys. Rev. A 94, 062703, (2016) [3] P. Yzombard et al., Phys. Rev. Lett. 114, 213001 (2015)