Exploring the dynamics of inelastic and reactive collisions on the quantum level is a fundamental goal in quantum chemistry. Such collisions are of particular importance in connection with Rydberg atoms in dense environments since they may considerably influence both the lifetime and the quantum state of the scattered Rydberg atoms. Here, we report on the study of state-changing collisions between Rydberg atoms and ground state atoms. We employ high-resolution momentum spectroscopy to identify the final states. In contrast to previous studies, we find that the outcome of such collisions is not limited to a single hydrogenic manifold. We observe a redistribution of population over a wide range of final states. We also find that even the decay to states with the same angular momentum quantum number as the initial state, but different principal quantum number is possible. We model the underlying physical process in the framework of a short-lived Rydberg quasi-molecular complex, where a charge exchange process gives rise to an oscillating electric field that causes transitions within the Rydberg manifold. The distribution of final states shows a diffusive-like behavior.
Combining ultracold atomic gases with the peculiar properties of Rydberg excited atoms gained a lot of theoretical and experimental attention in recent years. Embedded in the ultracold gas, an interaction between the Rydberg atom and the surrounding ground state atoms arises through the scattering of the Rydberg electron from an intruding perturber atom. This peculiar interaction gives rise to a plenitude of previously unobserved effects. Within the framework of the present thesis, this interaction is studied in detail for Rydberg
P-states in rubidium. Due to their long lifetime, atoms in Rydberg states are subject to scattering with the surrounding ground state atoms in the ultracold cloud. By measuring their lifetime as a function of the ground state atom flux, we are able to obtain the total inelastic scattering cross section as well as the partial cross section for associative ionisation. The fact that the latter is three orders of magnitude larger than the size of the formed molecular ion indicates the presence of an efficient mass transport mechanism that is mediated by the Rydberg–ground state interaction. The immense acceleration of the collisional process shows a close analogy to a catalytic process. The increase of the scattering cross section renders associative ionisation an important process that has to be considered for experiments in dense ultracold systems. The interaction of the Rydberg atom with a ground state perturber gives rise to a highly oscillatory potential that supports molecular bound states. These so-called ultralong-range Rydberg molecules are studied with high resolution time-of-flight spectroscopy, where we are able to determine the binding energies and lifetimes of the molecular states between the two fine structure split
25P-states. Inside an electric field, we observe a broadening of the molecular lines that indicates the presence of a permanent electric dipole moment, induced by the mixing with high angular momentum states. Due to the mixing of the ground state atom’s hyperfine states by the molecular interaction, we are able to observe a spin-flip of the perturber upon creation of a Rydberg molecule. Furthermore, an incidental near-degeneracy in the underlying level scheme of the
25P-state gives rise to highly entangled states between the Rydberg fine structure state and the perturber’s hyperfine structure. These mechanisms can be used to manipulate the quantum state of a remote particle over distances that exceed by far the typical contact interaction range. Apart from the ultralong-range Rydberg molecules that predominantly consist of only one low angular momentum state, a class of Rydberg molecules is predicted to exist that strongly mixes the high angular momentum states of the degenerate hydrogenic manifolds. These states, the so-called trilobite- and butterfly Rydberg molecules, show very peculiar properties that cannot be observed for conventional molecules. Here we present the first experimental observation of butterfly Rydberg molecules. In addition to an extensive spectroscopy that reveals the binding energy, we are also able to observe the rotational structure of these exotic molecules. The arising pendular states inside an electric field allow us, in comparison to the model of a dipolar rotor, to extract the precise bond length and dipole moment of the molecule. With the information obtained in the present study, it is possible to photoassociate butterfly molecules with a selectable bond length, vibrational state, rotational state, and orientation inside an electric field. By shedding light on various previously unrevealed aspects, the experiments presented in this thesis significantly deepen our knowledge on the Rydberg–ground state interaction and the peculiar effects arising from it. The obtained spectroscopic information on Rydberg molecules and the changed reaction dynamics for molecular ion creation will surely provide valuable data for quantum chemical simulations and provide necessary data to plan future experiments. Beyond that, our study reveals that the hyperfine interaction in Rydberg molecules and the peculiar properties of butterfly states provide very promising new ways to alter the short- and long-range interactions in ultracold many-body systems. In this sense the investigated Rydberg–ground state interaction not only lies right at the interface between quantum chemistry, quantum many-body systems, and Rydberg physics, but also creates many new and fascinating possibilities by combining these fields.
The theory of collisions of Rydberg atoms with rare-gas atoms is generalized to include the effects of an applied static electric field. Two effects occur. First, the field causes the states to split, and the increased energy separations lead to a decrease in the inelastic cross sections. Second, there is a change in the form of the wave functions, because the various Stark states in the field have electron charge distributions that may be localized in very different regions of space. The present work focuses on this second effect. With the description of the initial and final Stark states of the Rydberg atom by the proper electronic wave functions obtained in parabolic coordinates, cross sections are obtained for a variety of specific transitions of Rydberg atoms (
n=10,15,and20) caused by collisions. The calculations are strictly valid for hydrogen, but exhibit general features that are expected to apply to other Rydberg atoms as well. The results show a dramatic effect on the cross section for particular transitions depending on the degree of overlap of the initial and final charge distributions. In addition, it is observed that transitions are favored that involve small changes in the azimuthal quantum number
m. The origin of this tendency is discussed.
For $20\ensuremath{\le}n\ensuremath{\le}45$, two types of quasielastic state-changing-collisional (QESCC) processes, i.e., (i)
l-changing and (ii)
n-and
l-changing processes, have been theoretically investigated based on the free-electron model in which an excited Rydberg electron behaves as if it were "free" and slow with its interaction with a rare-gas atom playing a decisive role. It is shown that a parameter ${u}_{min}[=\frac{\ensuremath{\nu}{\ensuremath{\nu}}^{\ensuremath{'}}\ensuremath{\Delta}E{a}_{0}}{(\ensuremath{\hbar}V)}]$ is quite useful for characterizing both of these QESCC processes in a unified way where $\ensuremath{\nu}(\ensuremath{\simeq}{\ensuremath{\nu}}^{\ensuremath{'}})$ is an effective principal quantum number of the initial (final) state, $\ensuremath{\Delta}E$ is an energy defect, and
V is a relative velocity. It is theoretically found that higher-angular-momentum states are dominantly populated in the final channel of these QESCC processes with $1<{u}_{min}\ensuremath{\lesssim}\ensuremath{\nu}$ such as in the
n- and
l-changing collision of
Rb∗∗(ns)+He. This is in contrast with the uniform distribution over the final angular-momentum states for the usual
l-changing processes, i.e., ${u}_{min}\ensuremath{\lesssim}1$. The calculated cross sections of these QESCC processes with $1<{u}_{min}\ensuremath{\lesssim}\ensuremath{\nu}$ are found to be in reasonable agreement with experimental findings available at present.
Using state-selective field ionization, the state distributions of Rydberg atoms in cold Rydberg gases are measured for various initially excited Rydberg levels, populations, and evolution times. We provide direct experimental evidence for
l-changing collisions that we previously observed indirectly [S. K. Dutta, D. Feldbaum, A. Walz-Flannigan, J. R. Guest, and G. Raithel, Phys. Rev. Lett. 86, 3993 (2001)]. We also observe
n-mixing and find that its effects are largely in agreement with recent theoretical work on
n-changing collisions between electrons and Rydberg atoms, thus enabling an estimation of the electron temperature. Unexpectedly large populations of atoms are found in states with principal quantum numbers much lower than that of the initially excited atoms. We explain this observation by collisions between high-
l Rydberg atoms, which are highly polar and can collide due to static electric-dipole forces between them.
State changing of high-Rydberg atoms by collisions with rare-gas atoms have been theoretically investigated using the free-electron model. The non-selective character of transitions arising from the short range of the interaction between the high-Rydberg atoms and the rare-gas atoms is found to be strongly modified in the following two cases. First, for the high-Rydberg atoms in the circular states with | m |= l ≃ n , it has been found that transitions take place overwhelmingly between the circular states. This propensity rule originates from a highly anisotropic electron-density distribution of the initial circular states. Second, for the high-Rydberg states with large quantum defects (modulo 1), suppression of the yield of the lower angular momentum states have been observed. This cancels out the fair enhancement of the production of the high-Rydberg states with small | m | seen for the hydrogenic case with small quantum defects. It leads to the m distribution of the final states apparently proportional to their statistical weight.