Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

Physical Review A

Photoinitiated collisions between cold Cs Rydberg atoms

K. Richard Overstreet, Arne Schwettmann, Jonathan Tallant, James P. Shaffer

Published Jul 27, 2007• 47 citations
Publisher

Abstract

Experimental studies of a photoinitiated collision in an ultracold Cs Rydberg gas are presented. The process is characterized by measuring the laser intensity dependence of the absorption, the number of particles leaving each collision, and the recoil velocity of the collision fragments. The results of the experiment are compared to ab initio Rydberg pair interaction potentials.

DOI
10.1103/physreva.76.011403

Related papers

Inelastic Collisions in an Ultracold Cs Rydberg Gas

K. Richard Overstreet, Arne Schwettmann, Jonathan Tallant +1 more

We present measurements of inelastic collisions between ultracold Cs Rydberg atoms using time-of-flight velocity distributions. The collision mechanism is identified by comparison to Rydberg atom pair potentials calculated using matrix diagonalization.

Frontiers in Optics•Jan 1, 2006•0 citations

Long Range Interactions and Inelastic Collisions in a Cold Cs Rydberg Gas

James P. Shaffer, K. Richard Overstreet, Jonathan Tallant +2 more

Studies of cold Cs Rydberg atom elastic and inelastic collisions will be presented. Elastic collisions are investigated by observing spectral line broadening and shifts. Inelastic collisions are examined by measuring photofragment angle and velocity distributions.

Frontiers in Optics•Jan 1, 2005•0 citations

Pulsed excitation of Rydberg-atom-pair states in an ultracold Cs gas

Heiner Saßmannshausen, Frédéric Merkt, Johannes Deiglmayr

Pulsed laser excitation of a dense ultracold Cs vapor has been used to study the pairwise interactions between Cs atoms excited to $n{p}_{3/2}$ Rydberg states of principal quantum numbers in the range $n=22--36$. Molecular resonances were observed that correspond to excitation of Rydberg-atom-pair states correlated not only to the $n{p}_{3/2}+n{p}_{3/2}$ dissociation asymptotes, but also to $n{s}_{1/2}+(n+1){s}_{1/2}, n{s}_{1/2}+{n}^{\ensuremath{'}}{f}_{j}$, and $(n\ensuremath{-}4){f}_{j}+(n\ensuremath{-}3){f}_{j}\phantom{\rule{4pt}{0ex}}(j=5/2,7/2)$ dissociation asymptotes. These pair resonances are interpreted as arising from dipole-dipole and higher-order long-range-interaction terms between the Rydberg atoms on the basis of (i) their spectral positions, (ii) their response to static and pulsed electric fields, and (iii) millimeter-wave spectra between pair states correlated to different pair-dissociation asymptotes. The Rydberg-atom-pair states were found to spontaneously decay by Penning ionization and the dynamics of the ionization process were investigated during the first 15 $\ensuremath{\mu}\mathrm{s}$ following initial photoexcitation. To interpret the experimental observations, a potential model was derived that is based on the numerical determination of the eigenvalues and eigenfunctions of the long-range interaction Hamiltonian. With this potential model, which does not include adjustable parameters, all experimental observations could be accounted for, and the results demonstrate that long-range-interaction models provide a global and accurate description of interactions in ultracold Rydberg gases and that they correctly account for, and enable the analysis of, phenomena as diverse as the formation of Rydberg macrodimers, Penning ionization in dense Rydberg gases, and Rydberg-excitation-blockade effects.

arXiv:1506.08853•Physical Review A•Sep 8, 2015•14 citations

Emission of fast atoms from a cold Rydberg gas

Brenton Knuffman, Georg A. Raithel

Rydberg-Rydberg collisions in a cold, dense Rydberg gas can lead to the conversion of internal energy into center-of-mass energy of the colliding atoms, resulting in Rydberg-atom velocities much larger than the initial velocities in the gas. We prepare cold Rydberg-atom gases by laser excitation of laser-cooled atom clouds and use time-of-flight measurements to demonstrate the production of fast Rydberg atoms. The velocity distributions of Rydberg atoms emerging from the Rydberg-atom gases are obtained. State-selective field ionization spectra indicate a correlation between the production of fast Rydberg atoms and the presence of Penning ionization signatures. The dependence of the yield of fast Rydberg atoms on Rydberg atom density is measured.

Physical Review A•Feb 16, 2006•19 citations

Experimental studies of cesium Rydberg atom pair interactions

K. Richard Overstreet

This thesis describes experimental studies of Rydberg atom pair interactions. A new technique is described that combines trapping of ultracold Cesium atoms with Rydberg tagging time-of-flight spectroscopy to attain a velocity resolution of 2.5 cm/s. Using this technique, observed molecular resonances in Cesium spectra are characterized as either dissociating photo-initiated collision processes or bound long range Rydberg atom-Rydberg atom molecules called macrodimers.

•Jan 1, 2009•0 citations

Rydberg Molecules for Ion-Atom Scattering in the Ultracold Regime

T. Schmid, C. Veit, N. Zuber +4 more

We propose a novel experimental method to extend the investigation of ion-atom collisions from the so far studied cold, essentially classical regime to the ultracold, quantum regime. The key aspect of this method is the use of Rydberg molecules to initialize the ultracold ion-atom scattering event. We exemplify the proposed method with the lithium ion-atom system, for which we present simulations of how the initial Rydberg molecule wave function, freed by photoionization, evolves in the presence of the ion-atom scattering potential. We predict bounds for the ion-atom scattering length from ab initio calculations of the interaction potential. We demonstrate that, in the predicted bounds, the scattering length can be experimentally determined from the velocity of the scattered wave packet in the case of ^{6}Li^{+}-^{6}Li and from the molecular ion fraction in the case of ^{7}Li^{+}-^{7}Li. The proposed method to utilize Rydberg molecules for ultracold ion-atom scattering, here particularized for the lithium ion-atom system, is readily applicable to other ion-atom systems as well.

arXiv:1709.10488•Physical Review Letters•Apr 12, 2018•47 citations
Experimental studies of a photoinitiated collision in an ultracold Cs Rydberg gas are presented. The process is characterized by measuring the laser intensity dependence of the absorption, the number of particles leaving each collision, and the recoil velocity of the collision fragments. The results of the experiment are compared to ab initio Rydberg pair interaction potentials.
Pulsed laser excitation of a dense ultracold Cs vapor has been used to study the pairwise interactions between Cs atoms excited to np3/2n{p}_{3/2}np3/2​ Rydberg states of principal quantum numbers in the range n=22−−36n=22--36n=22−−36. Molecular resonances were observed that correspond to excitation of Rydberg-atom-pair states correlated not only to the np3/2+np3/2n{p}_{3/2}+n{p}_{3/2}np3/2​+np3/2​ dissociation asymptotes, but also to $n{s}_{1/2}+(n+1){s}_{1/2}, n{s}_{1/2}+{n}^{\ensuremath{'}}{f}_{j}$, and $(n\ensuremath{-}4){f}_{j}+(n\ensuremath{-}3){f}_{j}\phantom{\rule{4pt}{0ex}}(j=5/2,7/2)$ dissociation asymptotes. These pair resonances are interpreted as arising from dipole-dipole and higher-order long-range-interaction terms between the Rydberg atoms on the basis of (i) their spectral positions, (ii) their response to static and pulsed electric fields, and (iii) millimeter-wave spectra between pair states correlated to different pair-dissociation asymptotes. The Rydberg-atom-pair states were found to spontaneously decay by Penning ionization and the dynamics of the ionization process were investigated during the first 15 $\ensuremath{\mu}\mathrm{s}$ following initial photoexcitation. To interpret the experimental observations, a potential model was derived that is based on the numerical determination of the eigenvalues and eigenfunctions of the long-range interaction Hamiltonian. With this potential model, which does not include adjustable parameters, all experimental observations could be accounted for, and the results demonstrate that long-range-interaction models provide a global and accurate description of interactions in ultracold Rydberg gases and that they correctly account for, and enable the analysis of, phenomena as diverse as the formation of Rydberg macrodimers, Penning ionization in dense Rydberg gases, and Rydberg-excitation-blockade effects.
Rydberg-Rydberg collisions in a cold, dense Rydberg gas can lead to the conversion of internal energy into center-of-mass energy of the colliding atoms, resulting in Rydberg-atom velocities much larger than the initial velocities in the gas. We prepare cold Rydberg-atom gases by laser excitation of laser-cooled atom clouds and use time-of-flight measurements to demonstrate the production of fast Rydberg atoms. The velocity distributions of Rydberg atoms emerging from the Rydberg-atom gases are obtained. State-selective field ionization spectra indicate a correlation between the production of fast Rydberg atoms and the presence of Penning ionization signatures. The dependence of the yield of fast Rydberg atoms on Rydberg atom density is measured.
We propose a novel experimental method to extend the investigation of ion-atom collisions from the so far studied cold, essentially classical regime to the ultracold, quantum regime. The key aspect of this method is the use of Rydberg molecules to initialize the ultracold ion-atom scattering event. We exemplify the proposed method with the lithium ion-atom system, for which we present simulations of how the initial Rydberg molecule wave function, freed by photoionization, evolves in the presence of the ion-atom scattering potential. We predict bounds for the ion-atom scattering length from ab initio calculations of the interaction potential. We demonstrate that, in the predicted bounds, the scattering length can be experimentally determined from the velocity of the scattered wave packet in the case of ^{6}Li^{+}-^{6}Li and from the molecular ion fraction in the case of ^{7}Li^{+}-^{7}Li. The proposed method to utilize Rydberg molecules for ultracold ion-atom scattering, here particularized for the lithium ion-atom system, is readily applicable to other ion-atom systems as well.