Lothar Ratschbacher

Controlling chemical reactions of a single particle

Lothar Ratschbacher [1], Christoph Zipkes [1], Carlo Sias [1], Michael Köhl

Abstract

The control of chemical reactions is a recurring theme in physics and chemistry. Traditionally, chemical reactions have been investigated by tuning thermodynamic parameters, such as temperature or pressure. More recently, physical methods such as laser or magnetic field control have emerged to provide completely new experimental possibilities, in particular in the realm of cold collisions. The control of reaction pathways is also a critical component to implement molecular quantum information processing. For these undertakings, single particles provide a clean and well-controlled experimental system. Here, we report on the experimental tuning of the exchange reaction rates of a single trapped ion with ultracold neutral atoms by exerting control over both their quantum states. We observe the influence of the hyperfine interaction on chemical reaction rates and branching ratios, and monitor the kinematics of the reaction products. These investigations advance chemistry with single trapped particles towards achieving quantum-limited control of chemical reactions and indicate limits for buffer gas cooling of single ion clocks.

Kinetics of a single trapped ion in an ultracold buffer gas

Christoph Zipkes [1], Lothar Ratschbacher [1], Carlo Sias [1], Michael Köhl

Abstract

The immersion of a single ion confined by a radiofrequency trap in an ultracold atomic gas extends the concept of buffer gas cooling to a new temperature regime. The steady state energy distribution of the ion is determined by its kinetics in the radiofrequency field rather than the temperature of the buffer gas. Moreover, the finite size of the ultracold gas facilitates the observation of back-action of the ion onto the buffer gas. We numerically investigate the system's properties depending on atom-ion mass ratio, trap geometry, differential cross-section, and non-uniform neutral atom density distribution. Experimental results are well reproduced by our model considering only elastic collisions. We identify excess micromotion to set the typical scale for the ion energy statistics and explore the applicability of the mobility collision cross-section to the ultracold regime.

Hybrid quantum systems of atoms and ions

Christoph Zipkes [1], Lothar Ratschbacher [1], Stefan Palzer [1], Carlo Sias [1], Michael Köhl

Abstract

In recent years, ultracold atoms have emerged as an exceptionally controllable experimental system to investigate fundamental physics, ranging from quantum information science to simulations of condensed matter models. Here we go one step further and explore how cold atoms can be combined with other quantum systems to create new quantum hybrids with tailored properties. Coupling atomic quantum many-body states to an independently controllable single-particle gives access to a wealth of novel physics and to completely new detection and manipulation techniques. We report on recent experiments in which we have for the first time deterministically placed a single ion into an atomic Bose Einstein condensate. A trapped ion, which currently constitutes the most pristine single particle quantum system, can be observed and manipulated at the single particle level. In this single-particle/many-body composite quantum system we show sympathetic cooling of the ion and observe chemical reactions of single particles in situ.

Cold heteronuclear atom-ion collisions

Christoph Zipkes [1], Stefan Palzer [1], Lothar Ratschbacher [1], Carlo Sias [1], Michael Köhl

Abstract

We study cold heteronuclear atom ion collisions by immersing a trapped single ion into an ultracold atomic cloud. Using ultracold atoms as reaction targets, our measurement is sensitive to elastic collisions with extremely small energy transfer. The observed energy-dependent elastic atom-ion scattering rate deviates significantly from the prediction of Langevin but is in full agreement with the quantum mechanical cross section. Additionally, we characterize inelastic collisions leading to chemical reactions at the single particle level and measure the energy-dependent reaction rate constants. The reaction products are identified by in-trap mass spectrometry, revealing the branching ratio between radiative and non-radiative charge exchange processes.