Coherent Structural Dynamics of Rydberg-Excited Molecules

Ivan Mirgorodskiy, Florian Christaller, Christoph Braun +3 more

We study the impact of Rydberg molecule formation on the storage and retrieval of Rydberg polaritons in an ultracold atomic medium. We observe coherent revivals appearing in the storage and retrieval efficiency of stored photons that originate from simultaneous excitation of Rydberg atoms and Rydberg molecules in the system with subsequent interference between the possible storage paths. We show that over a large range of principal quantum numbers the observed results can be described by a two-state model including only the atomic Rydberg state and the Rydberg dimer molecule state. At higher principal quantum numbers the influence of polyatomic molecules becomes relevant and the dynamics of the system undergoes a transition from coherent evolution of a few-state system to an effective dephasing into a continuum of molecular states.

Gerard T. Higgins

Hanspeter Helm

Björn Butscher

In the course of this thesis the techniques of coherent state preparation and interrogation introduced by Stern, Rabi, Ramsey and others are extended to large samples of ultracold Rydberg atoms and molecules. The key technique to realize the coherent control is a Ramsey-like excitation scheme. To achieve this, a Rydberg interferometer is set up and successfully applied in the investigation of the recently discovered ultralong-range Rydberg molecules as well as for the exploration of the dynamics of atomic Rydberg states. Therby, the coherent control of Rydberg molecules is proven. This is a major step towards time resolved investigation of the dynamics of the exotic molecule and opens new opportunities for a more sophisticated understanding of the underlying binding mechanisms. The first experimental application of the interferometer has been given for ultralong-range Rydberg molecules. Following the work of Ramsey, an experimental sequence with two excitation pulses split in time was set up. Because the Rydberg molecules are coherently photoassociated in the experiment, an interference pattern known as Ramsey fringes is created. The loss of visibility of the Ramsey fringe pattern could be described in a two-level model and from these calculations, the lifetime of the molecules was determined interferometrically. Thus aside from being an elegant and unambiguous proof for the coherence of the photoassociation, the occurrence of Ramsey fringes also allows one to see the experiment as an atom-molecule interferometer. These experiments have paved the way towards experimental exploration of the dynamics of these exotic molecule. For another open question in the field of ultralong-range Rydberg molecules - their lifetime - the findings in this thesis brought clarity. From the density-dependent investigations it could be found that the lifetime of the vibrationally excited molecular state is systematically shorter than that of the molecular ground state. These findings confirm the theory that the excited molecular states are bound by quantum reflection: The shortened lifetime can be ascribed to the inward penetration of the bound atomic pair due to imperfect quantum reflection leading to the dissociation of the molecule. In the further course of this thesis, the idea of a Ramsey setup for Rydberg molecules has been extend to Rydberg atoms. With the introduction of a control parameter to tune the relative phase shift between the ground-state arm and the Rydberg arm, the so far empty interferometer has been extended to a full working interferometer. The measurements on the 43s-state in electric fields demonstrated the usability of the interferometer in a simple and well controllable system and the interferometric studies on the 46d-state in crossed external fields can be regarded as the first investigative application of the interferometer. The key point of the investigation is the link between the two observables of the Rydberg interferometer, phase shift and visibility, and the complex value describing the Rydberg state of interest. It was found that the phase shift of the Rydberg state mostly follows the adiabatic energy curves in the electric field calculated for these experimental parameters. However, in the region where avoided crossings du to crossed electric and magnetic field occur, the phase shift behaves substantially different. While the phase rises fast by pi near one avoided crossing, a 2pi jump occurs at another avoided crossing. Since the phase can only be determined in the interval between 0 and 2pi experimentally, the jump cannot be observed as function of the electric field. This limitation has been overcome by taking the phase shift as function of time for different electric fields, which allows to reconstruct the phase at the given field-on time independently. From these measurements, the occurrence of the 2pi jump could be validated. To explore the reasons underlying the behavior of the phase in the electric field, the dynamics of the system has been modeled theoretically. The experimental findings for the phase shift as well as for the visibility are thoroughly reproduced by theory. Especially the characteristic behavior of phase shift and visibility near the avoided crossings is also seen in the calculations. With the help of this modeling one can see the fast pi rise in analogy to the phase of a driven harmonic oscillator that changes from in-phase when the driving frequency is below the resonance of the oscillator and out-of-phase above. The 2pi jump, however, emerges from the complex dynamics of the several levels involved and can not be easily broken down to a two-level picture. Altogether, these findings confirm that the Rydberg interferometer can track the dynamics of the selected Rydberg state and enabled the tomography of the Rydberg state. Moreover, these measurements show the potential of the Rydberg interferometer as tool to explore the dynamic of quantum systems.

Todd A. Johnson, Erich Urban, Thomas Henage +4 more

Francisco Camargo

In this work I describe the excitation spectra of Rydberg atoms in ultracold gases of strontium and their decay mechanisms. In a few-body regime, we observe a highly structured spectrum re ecting excitation of ultralong-range molecules consisting of one or more ground-state atoms bound to the Rydberg core in potential wells formed by the Rydbergelectron wave function. In a many-body regime, with hundreds of ground-state atoms within the Rydberg orbital, the Rydberg atoms can be viewed as an impurity in a quantum gas, connecting to important concepts in condensed matter physics. The spectrum for impurity excitation displays signatures of polaronic states, in which the Rydberg atom signi cantly perturbs the density of the background gas. Additionally, decay channels of Rydberg excitations are examined by monitoring the time evolution of Rydberg populations. The measured lifetimes reveal new information on the decay processes of Rydberg molecules and place limits on the time scales over which studies involving Rydberg species in cold, dense atomic gases can be undertaken and limit the coherence times for such measurements.