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arXiv:1901.08781 · Journal of Physics B Atomic Molecular and Optical Physics

Optical control of atom-ion collisions using a Rydberg state

Limei Wang, Markus Deiß, Georg A. Raithel, Johannes Hecker Denschlag

Published Mar 5, 2020• 15 citations
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Abstract

Abstract We present a method to control collisions between ultracold neutral atoms in the electronic ground state and trapped ions. During the collision, the neutral atom is resonantly excited by a laser to a low-field-seeking Rydberg state, which is repelled by the ion. As the atom is reflected from the ion, it is de-excited back into its electronic ground level. The efficiency of shielding is analyzed as a function of laser frequency and power, initial atom-ion collision energy, and collision angle. The suitability of several Rydberg levels of Na and Rb for shielding is discussed. Useful applications of shielding include the suppression of unwanted chemical reactions between atoms and ions, a prerequisite for controlled atom-ion interactions.

DOI
10.1088/1361-6455/ab7d24

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arXiv:1709.00775•Sep 3, 2017•2 citations
Abstract We present a method to control collisions between ultracold neutral atoms in the electronic ground state and trapped ions. During the collision, the neutral atom is resonantly excited by a laser to a low-field-seeking Rydberg state, which is repelled by the ion. As the atom is reflected from the ion, it is de-excited back into its electronic ground level. The efficiency of shielding is analyzed as a function of laser frequency and power, initial atom-ion collision energy, and collision angle. The suitability of several Rydberg levels of Na and Rb for shielding is discussed. Useful applications of shielding include the suppression of unwanted chemical reactions between atoms and ions, a prerequisite for controlled atom-ion interactions.
We present a method to control the cold collision between an ultracold atom and a trapped ion. A laser is used to excite the ground state atom to a repulsive Rydberg potential level at a certain atom-ion distance. In this way the ion is effectively surrounded by a potential wall that the atom cannot cross. Once the atom leaves the interaction area, it is de-excited back to its original level. The adiabaticity of the scheme is analyzed as a function of different parameters such as laser frequency, laser power, initial atom-ion collision energy, as well as the direction of the collisional process with respect to the light field. By controlling e.g. the laser power and the laser frequency, as well as by addressing different Rydberg states, the properties of this shielding effect can be widely tuned. In particular, unwanted chemical reactions between atoms and ion can efficiently be suppressed, which is an important step towards realization of diverse quantum technological applications for hybrid atom-ion systems.
We propose a method to suppress the chemical reactions between ultracold bosonic ground-state ^{23}Na^{87}Rb molecules based on optical shielding. By applying a laser with a frequency blue-detuned from the transition between the lowest rovibrational level of the electronic ground state X^{1}Σ^{+}(v_{X}=0,j_{X}=0), and the long-lived excited level b^{3}Π_{0}(v_{b}=0,j_{b}=1), the long-range dipole-dipole interaction between the colliding molecules can be engineered, leading to a dramatic suppression of reactive and photoinduced inelastic collisions, for both linear and circular laser polarizations. We demonstrate that the spontaneous emission from b^{3}Π_{0}(v_{b}=0,j_{b}=1) does not deteriorate the shielding process. This opens the possibility for a strong increase of the lifetime of cold molecule traps and for an efficient evaporative cooling. We also anticipate that the proposed mechanism is valid for alkali-metal diatomics with sufficiently large dipole-dipole interactions.
Atoms in highly excited Rydberg states possess physical characteristics quite unlike those associated with atoms in the ground or low-lying excited states. In particular, they are physically very large and are only very weakly bound. In consequence, collisions can lead to a wide variety of reaction processes many of which are unique to Rydberg species and have very large collision cross sections. In collisions with neutral targets, Rydberg atoms behave not as an atom but rather as a pair of well-separated independent scatterers, namely the core ion and the excited Rydberg electron. In the present article we discuss many of the different reactions that can occur when Rydberg atoms collide with neutral targets, focusing principally on reactions that are dominated by (binary) Rydberg electron-target interactions and include collisions with molecules that attach free low-energy electrons and with polar targets. In certain situations, however, interactions involving the Rydberg core ion are important. This is illustrated using as an example the destruction of ultralong-range Rydberg molecules excited in a cold dense gas.
We report on the observation of interactions between ultracold Rydberg atoms and ions in a Paul trap. The rate of observed inelastic collisions, which manifest themselves as charge transfer between the Rydberg atoms and ions, exceeds that of Langevin collisions for ground state atoms by about 3 orders of magnitude. This indicates a huge increase in interaction strength. We study the effect of the vacant Paul trap's electric fields on the Rydberg excitation spectra. To quantitatively describe the exhibited shape of the ion loss spectra, we need to include the ion-induced Stark shift on the Rydberg atoms. Furthermore, we demonstrate Rydberg excitation on a dipole-forbidden transition with the aid of the electric field of a single trapped ion. Our results confirm that interactions between ultracold atoms and trapped ions can be controlled by laser coupling to Rydberg states. Adding dynamic Rydberg dressing may allow for the creation of spin-spin interactions between atoms and ions, and the elimination of collisional heating due to ionic micromotion in atom-ion mixtures.
Abstract In excited molecules, the interaction between the covalent Rydberg and ion-pair channels forms a unique class of excited states, in which the infinite manifold of vibrational levels are the equivalent of atomic Rydberg states with a heavy electron mass. Production of the ion-pair states usually requires excitation through one or several interacting Rydberg states; these interacting channels lead to loss of flux, diminishing the rate of ion-pair production. Here, we develop an analytical, asymptotic charge-transfer model for the interaction between ultracold Rydberg molecular states, and employ this method to demonstrate the utility of off-resonant field control over the ion-pair formation, with near unity efficiency.
The control of the ultracold collisions between neutral atoms is an extensive and successful field of study. The tools developed allow for ultracold chemical reactions to be managed using magnetic fields, light fields and spin-state manipulation of the colliding particles among other methods. The control of chemical reactions in ultracold atom-ion collisions is a young and growing field of research. Recently, the collision energy and the ion electronic state were used to control atom-ion interactions. Here, we demonstrate spin-controlled atom-ion inelastic processes. In our experiment, both spin-exchange and charge-exchange reactions are controlled in an ultracold Rb-Sr+^++ mixture by the atomic spin state. We prepare a cloud of atoms in a single hyperfine spin-state. Spin-exchange collisions between atoms and ion subsequently polarize the ion spin. Electron transfer is only allowed for (RbSr)+^++ colliding in the singlet manifold. Initializing the atoms in various spin states affects the overlap of the collision wavefunction with the singlet molecular manifold and therefore also the reaction rate. We experimentally show that by preparing the atoms in different spin states one can vary the charge-exchange rate in agreement with theoretical predictions.