arXiv subjects

Johannes Deiglmayr

Publications and source records attributed to Johannes Deiglmayr.

26 records · Page 2Linked to original sources

arXiv2014

Manipulating Rydberg atoms close to surfaces at cryogenic temperatures

Helium atoms in Rydberg states have been manipulated coherently with microwave radiation pulses near a gold surface and near a superconducting NbTiN surface at a temperature of $3 \text{K}$. The experiments were carried out with a skimmed supersonic beam of metastable $(1\text{s})^1(2\text{s})^1\, {}^1\text{S}_0$ helium atoms excited with laser radiation to $n\text{p}$ Rydberg levels with principal quantum number $n$ between $30$ and $40$. The separation between the cold surface and the center of the collimated beam is adjustable down to $250 μ\text{m}$. Short-lived $n\text{p}$ Rydberg levels were coherently transferred to the long-lived $n\text{s}$ state to avoid radiative decay of the Rydberg atoms between the photoexcitation region and the region above the cold surfaces. Further coherent manipulation of the $n\text{s}$ Rydberg levels with pulsed microwave radiation above the surfaces enabled measurements of stray electric fields and allowed us to study the decoherence of the atomic ensemble. Adsorption of residual gas onto the surfaces and the resulting slow build-up of stray fields was minimized by controlling the temperature of the surface and monitoring the partial pressures of H$_2$O, N$_2$, O$_2$ and CO$_2$ in the experimental chamber during the cool-down. Compensation of the stray electric fields to levels below $100 \text{mV}/\text{cm}$ was achieved over a region of $6 \text{mm}$ along the beam-propagation direction which, for the $1770 \text{m}/\text{s}$ beam velocity, implies the possibility to preserve the coherence of the atomic sample for several microseconds above the cold surfaces.

physics.atom-ph↗

arXiv2012

Reactive collisions of trapped anions with ultracold atoms

We present a scheme to embed molecular anions in a gas of ultracold rubidium atoms as a route towards the preparation of cold molecular ions by collisional cooling with ultracold atoms. Associative detachment as an important loss process in collisions between OH- molecules and rubidium atoms is studied. The density distribution of trapped negative ions in the multipole radiofrequency trap is measured by photodetachment tomography, which allows us to derive absolute rate coefficients for the process. We define a regime where translational and internal cooling of molecular ions embedded into the ultracold atomic cloud can be achieved.

physics.atom-ph↗

arXiv2009

Core repulsion effects in alkali trimers

The present paper is related to a talk presented during the Symposium on Coherent Control and Ultracold Chemistry held during the Sixth Congress of the International Society for Theoretical Chemical Physics (ISTCP-VI, July 2008). The talk was entitled "Electronic structure properties of alkali dimers and trimers. Prospects for alignment of ultracold molecules". Here we report on the electrostatic repulsion forces of the ionic cores at short separation, involved when the potential energy surfaces of alkali trimers are calculated with a quantum chemistry approach based on effective large-core potentials for ionic core description. We demonstrate that such forces in the triatomic molecule can be obtained as the sum of three pairwise terms. We illustrate our results on the lowest electronic states of Cs$_3$, which are computed for the first time within a full configuration interaction based on a large Gaussian basis set. As a preliminary section, we also propose a brief introduction about the importance of alkali trimer systems in the context of cold and ultracold molecules.

physics.atm-clus↗

arXiv2009

Systematic trends in electronic properties of alkali hydrides

Obtaining ultracold samples of dipolar molecules is a current challenge which requires an accurate knowledge of their electronic properties to guide the ongoing experiments. Alkali hydride molecules have permanent dipole significantly larger than those of mixed alkali species and, as pointed out by Taylor-Juarros et al. [Eur. Phys. J. D 31, 213 (2004)] and by Juarros et al. [Phys. Rev. A 73, 041403 (2006)], are thus good candidates for molecule formation. In this paper, using a standard quantum chemistry approach based on pseudopotentials for atomic core representation, large Gaussian basis sets, and effective core polarization potential, we systematically investigate the electronic properties of the alkali hydrides LiH to CsH, in order to discuss general trends of their behavior. We computed (for the first time for NaH, KH, RbH, and CsH) the variation of their static polarizability with the internuclear distance. Moreover, in addition to potential curves, we determine accurate values of permanent and transition dipole moments for ground and excited states depending on the internuclear distance. The behavior of electronic properties of all alkali hydrides is compared to each other, in the light of the numerous other data available in the literature. Finally, the influence of the quality of the representation of the hydrogen electronic affinity in the approach on the results is discussed.

physics.atom-ph↗

arXiv2008

Calculations of static dipole polarizabilities of alkali dimers. Prospects for alignment of ultracold molecules

The rapid development of experimental techniques to produce ultracold alkali molecules opens the ways to manipulate them and to control their dynamics using external electric fields. A prerequisite quantity for such studies is the knowledge of their static dipole polarizabilities. In this paper, we computed the variations with internuclear distance and with vibrational index of the static dipole polarizability components of all homonuclear alkali dimers including Fr$_2$, and of all heteronuclear alkali dimers involving Li to Cs, in their electronic ground state and in their lowest triplet state. We use the same quantum chemistry approach than in our work on dipole moments (M. Aymar and O. Dulieu, J. Chem. Phys. 122, 204302 (2005)), based on pseudopotentials for atomic core representation, Gaussian basis sets, and effective potentials for core polarization. Polarizabilities are extracted from electronic energies using the finite-field method. For the heaviest species Rb$_2$, Cs$_2$ and Fr$_2$ and for all heteronuclear alkali dimers, such results are presented for the first time. The accuracy of our results on atomic and molecular static dipole polarizabilities is discussed by comparing our values with the few available experimental data and elaborate calculations. We found that for all alkali pairs, the parallel and perpendicular components of the ground state polarizabilities at the equilibrium distance $R_e$ scale as $(R_e)^3$, which can be related to a simple electrostatic model of an ellipsoidal charge distribution. Prospects for possible alignment and orientation effects with these molecules in forthcoming experiments are discussed.

physics.atom-ph↗

arXiv2008

Rabi oscillations between ground and Rydberg states and van der Waals blockade in a mesoscopic frozen Rydberg gas

We present a detailed analysis of our recent observation of synchronous Rabi oscillations between the electronic ground state and Rydberg states in a mesoscopic ensemble containing roughly 100 ultracold atoms [M. Reetz-Lamour \textit{et al.}, submitted, arXiv:0711.4321]. The mesoscopic cloud is selected out of a sample of laser-cooled Rb atoms by optical pumping. The atoms are coupled to a Rydberg state with principal quantum number around 30 by a two-photon scheme employing flat-top laser beams. The influence of residual spatial intensity fluctuations as well as sources of decoherence such as redistribution to other states, radiative lifetime, and laser bandwidth are analysed. The results open up new possibilities for the investigation of coherent many-body phenomena in dipolar Rydberg gases. As an example we demonstrate the van der Waals blockade, a variant of the dipole blockade, for a mesoscopic atom sample.

physics.atom-ph↗

arXiv2008

Rabi oscillations and excitation trapping in the coherent excitation of a mesoscopic frozen Rydberg gas

We demonstrate the coherent excitation of a mesoscopic ensemble of about 100 ultracold atoms to Rydberg states by driving Rabi oscillations from the atomic ground state. We employ a dedicated beam shaping and optical pumping scheme to compensate for the small transition matrix element. We study the excitation in a weakly interacting regime and in the regime of strong interactions. When increasing the interaction strength by pair state resonances we observe an increased excitation rate through coupling to high angular momentum states. This effect is in contrast to the proposed and previously observed interaction-induced suppression of excitation, the so-called dipole blockade.

physics.atom-ph↗

arXiv2007

A high resolution time-of-flight mass spectrometer for the detection of ultracold molecules

We have realized a high-resolution time-of-flight mass spectrometer combined with a magneto-optical trap. The spectrometer enables excellent optical access to the trapped atomic cloud using specifically devised acceleration and deflection electrodes. The ions are extracted along a laser beam axis and deflected onto an off axis detector. The setup is applied to detect atoms and molecules photoassociated from ultracold atoms. The detection is based on resonance-enhanced multi-photon ionization. Mass resolution up to m/Delta m_rms = 1000 at the mass of 133Cs is achieved. The performance of this spectrometer is demonstrated in the detection of photoassociated ultracold 7Li133Cs molecules near a large signal of 133Cs ions.

physics.atom-ph↗