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A Rydberg impurity in a dense background gas (Conference Presentation)

Tara Cubel Liebisch, Michael Schlagmüller, Felix Engel, Karl Westphal, K. S. Kleinbach, Fabian Böttcher, Robert Loew, Sebastian Hofferberth, Tilman Pfau, Jesús Pérez‐Ríos, Chris H. Greene

Published Aug 3, 2016• 0 citations
Publisher

Abstract

A single Rydberg atom impurity excited in a BEC is a system that can be utilized to measure the quantum mechanical properties of electron - neutral scattering andthe electron probability density of a Rydberg atom. The Rydberg electron – neutral atom scattering process, is a fundamental scattering process, which can be described via Fermi’s pseudopotential as V{vec{r},vec{R} )=2pi textit{a}[k(R)]delta^{(3)}(vec{r}-vec{R}). The scattering length is dependent on the momentum of the Rydberg electron, and therefore is dependent on the separation of the Rydberg electron from the ion core. At the classical outermost turning point of the electron, it has the slowest momentum leading to s-wave dominated scattering potentials 10’s of MHz in depth for n<40 (Greene et al. PRL 85 2458 (2000), Bendkowsky et al. PRL 105 163201 (2010)). In alkali atoms there is a shape resonance for p-wave scattering, which becomes relevant at ion-neutral separations of ~75nm (I.I. Fabrikant J.Phys B 19, 1527 (1985)). This shape resonance potential is several GHz deep, spanning the energy level spacing between n and n-1 principal quantum numbers. At high BEC densities of 5x10^14cm-3 the nearest neighbor spacing is less than 70nm. A Rydberg atom excited within a BEC, is an excitation of the Rydberg atom and all N neutral atoms located within the Rydberg orbit, described as nS+N x 5S. The nS+N x 5S state is density shifted from the Rydberg resonance. Not only does the distribution of atoms within the Rydberg orbit lead to a density shift, but, at these high densities, atoms excited in the nS+N x 5S state near the shape resonance potential cause large perturbations to the density shift, leading to a line broadening. Therefore the spectroscopic line shape of a Rydberg atom in a BEC allows us to probe the theoretically calculated p-wave shape resonance potential. Furthermore, we can observe and measure the dynamics of neutrals excited in the nS+N x 5S state. In the ultracold regime of a BEC, the background neutral atoms within the Rydberg orbit have kinetic energies of a few kHz, and experience large forces due to the GHz-deep shape resonance potentials. An atom dragged into this deep potential leads to an exothermic state-changing collision. We measure the timescale of this state-changing collision and compare to semi-classical calculations of the neutral atoms evolving in the potential of the two-particle nS+ 5S system. We also measure the change in energy from the original nS state to the product state, (n-4)L (L<3). On time scales shorter than the state-changing collisions, which for n<100 is on the order of 10 microseconds, the neutral atoms will evolve and collect in the shallower electron-neutral potentials, which mimic the electron probability density of the Rydberg atom.With n<100, the Rydberg atom has a diameter greater than 2 micrometers. With an imaging system with <1 micrometer resolution, we expect to observe a macroscopic change in the density profile of the BEC indicating an nS versus nD Rydberg state. The BEC would serve as a contrast agent for observing textbook atomic wavefunctions (Karpiuk et al. New Journal of Physics 17, 053046 (2015)).

DOI
10.1117/12.2227722

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A single Rydberg atom impurity excited in a BEC is a system that can be utilized to measure the quantum mechanical properties of electron - neutral scattering andthe electron probability density of a Rydberg atom. The Rydberg electron – neutral atom scattering process, is a fundamental scattering process, which can be described via Fermi’s pseudopotential as V{vec{r},vec{R} )=2pi textit{a}[k(R)]delta^{(3)}(vec{r}-vec{R}). The scattering length is dependent on the momentum of the Rydberg electron, and therefore is dependent on the separation of the Rydberg electron from the ion core. At the classical outermost turning point of the electron, it has the slowest momentum leading to s-wave dominated scattering potentials 10’s of MHz in depth for n<40 (Greene et al. PRL 85 2458 (2000), Bendkowsky et al. PRL 105 163201 (2010)). In alkali atoms there is a shape resonance for p-wave scattering, which becomes relevant at ion-neutral separations of ~75nm (I.I. Fabrikant J.Phys B 19, 1527 (1985)). This shape resonance potential is several GHz deep, spanning the energy level spacing between n and n-1 principal quantum numbers. At high BEC densities of 5x10^14cm-3 the nearest neighbor spacing is less than 70nm. A Rydberg atom excited within a BEC, is an excitation of the Rydberg atom and all N neutral atoms located within the Rydberg orbit, described as nS+N x 5S. The nS+N x 5S state is density shifted from the Rydberg resonance. Not only does the distribution of atoms within the Rydberg orbit lead to a density shift, but, at these high densities, atoms excited in the nS+N x 5S state near the shape resonance potential cause large perturbations to the density shift, leading to a line broadening. Therefore the spectroscopic line shape of a Rydberg atom in a BEC allows us to probe the theoretically calculated p-wave shape resonance potential. Furthermore, we can observe and measure the dynamics of neutrals excited in the nS+N x 5S state. In the ultracold regime of a BEC, the background neutral atoms within the Rydberg orbit have kinetic energies of a few kHz, and experience large forces due to the GHz-deep shape resonance potentials. An atom dragged into this deep potential leads to an exothermic state-changing collision. We measure the timescale of this state-changing collision and compare to semi-classical calculations of the neutral atoms evolving in the potential of the two-particle nS+ 5S system. We also measure the change in energy from the original nS state to the product state, (n-4)L (L<3). On time scales shorter than the state-changing collisions, which for n<100 is on the order of 10 microseconds, the neutral atoms will evolve and collect in the shallower electron-neutral potentials, which mimic the electron probability density of the Rydberg atom.With n<100, the Rydberg atom has a diameter greater than 2 micrometers. With an imaging system with <1 micrometer resolution, we expect to observe a macroscopic change in the density profile of the BEC indicating an nS versus nD Rydberg state. The BEC would serve as a contrast agent for observing textbook atomic wavefunctions (Karpiuk et al. New Journal of Physics 17, 053046 (2015)).
We present spectroscopy of a single Rydberg atom excited within a Bose-Einstein condensate. We not only observe the density shift as discovered by Amaldi and Segrè in 1934, but a line shape that changes with the principal quantum number n. The line broadening depends precisely on the interaction potential energy curves of the Rydberg electron with the neutral atom perturbers. In particular, we show the relevance of the triplet p-wave shape resonance in the e^{-}-Rb(5S) scattering, which significantly modifies the interaction potential. With a peak density of 5.5×10^{14} cm^{-3}, and therefore an interparticle spacing of 1300 a_{0} within a Bose-Einstein condensate, the potential energy curves can be probed at these Rydberg ion-neutral atom separations. We present a simple microscopic model for the spectroscopic line shape by treating the atoms overlapped with the Rydberg orbit as zero-velocity, uncorrelated, pointlike particles, with binding energies associated with their ion-neutral separation, and good agreement is found.
A single Rydberg excitation in the high-density and low-temperature environment of a Bose-Einstein condensate (BEC) leads to a fascinating testbed of low-energy electron-neutral and ion-neutral scattering. In particular the small interparticle spacing in a BEC makes it possible to study the role of ion-neutral interactions in l-changing collisions on time scales much shorter than the Rydberg lifetime. We take advantage of the mean field density shift, caused by elastic electron-neutral collisions, to probe density dependent shells of the 87^{87}87Rb BEC and thereby measure the l-changing collision time versus density and principal quantum number. We report on l-changing collisions due to inelastic scattering of the Rydberg electron with a neutral atom located near the Rydberg ionic core. We measure timescales of both the l-changing collision and the Rb2_{2}2​ molecule formation of less than one microsecond for n <<< 100 at the highest BEC densities. We extract a change in kinetic energy of the Rydberg atoms that matches well with the energy gap to the next-lowest manifold. We measure Rb2_{2}2​ signal that decreases with increasing principal quantum number. The mechanism and timescales of the l-changing collision are compared with simulations including the motion of the ionic core and neutral atoms, as well as the Rydberg electron.
Rydberg atoms immersed in a Bose-Einstein condensate interact with the quantum gas via electron-atom and ion-atom interaction. To suppress the typically dominant electron-neutral interaction, Rydberg states with a principal quantum number up to n=190 are excited from a dense and tightly trapped micron-sized condensate. This allows us to explore a regime where the Rydberg orbit exceeds the size of the atomic sample by far. In this case, a detailed line shape analysis of the Rydberg excitation spectrum provides clear evidence for ion-atom interaction at temperatures well below a microkelvin. Our results may open up ways to enter the quantum regime of ion-atom scattering for the exploration of charged quantum impurities and associated polaron physics.
Within a dense environment (ρ ≈ 10 14 atoms=cm 3 ) at ultracold temperatures (T < 1 μK), a single atom excited to a Rydberg state acts as a reaction center for surrounding neutral atoms.At these temperatures, almost all neutral atoms within the Rydberg orbit are bound to the Rydberg core and interact with the Rydberg atom.We have studied the reaction rate and products for nS 87 Rb Rydberg states, and we mainly observe a state change of the Rydberg electron to a high orbital angular momentum l, with the released energy being converted into kinetic energy of the Rydberg atom.Unexpectedly, the measurements show a threshold behavior at n ≈ 100 for the inelastic collision time leading to increased lifetimes of the Rydberg state independent of the densities investigated.Even at very high densities (ρ ≈ 4.8 × 10 14 cm -3 ), the lifetime of a Rydberg atom exceeds 10 μs at n > 140 compared to 1 μs at n ¼ 90.In addition, a second observed reaction mechanism, namely, Rb þ 2 molecule formation, was studied.Both reaction products are equally probable for n ¼ 40, but the fraction of Rb þ 2 created drops to below 10% for n ≥ 90.
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.
Rydberg atom, with a large principal quantum number n, has big size, long lifetime, strong long-range interactions, and so on. These properties make Rydberg atoms potential candidate of quantum gate and single-photon source. Rydberg electron can interact with nearby ground-state atom, which is polarized by the Rydberg electron and is bound to the orbit of Rydberg electrons forming Rydberg molecule. As the kinetic energy of the Rydberg electron is very low, only the lowest partial waves will contribute to the molecular potential.#br#In this paper, the low electron-atom scattering with the semi-classical approximation is introduced, and the pseudopotential of interaction between Rydberg electron and ground-state atom is used to describe the long-range Rydberg molecular potential. Molecular potential curves for cesium (nS, n=30-60) are plotted according to the results of numerical computation, from which the outermost potential depth De and the equilibrium distance r0 of long-range cesium Rydberg molecule are deduced. Potential curves of cesium Rydberg molecules are consistent with the distribution curves in radial probability densities of cesium Rydberg electrons. Dependences of De and r0 on the principal quantum number n are investigated, this has an important role for the experimental measurements. The size of a Rydberg molecule depends on the equilibrium distance r0 and is proportional to the square of effective principal quantum number (n-δ )2. The calculated outermost potential depth De of Rydberg molecule becomes smaller with the increase of principal quantum number n. Rydberg molecule is very sensitive to the external field and can be used to measure and monitor weak signals.