Chris H. Greene

Barium Autoionization for Efficient Ion Trap Loading

Zachary J. Wall [1], Justin D. Piel [2], Samuel R. Vizvary [1], Michael Bareian [1], Steven Diaz [1], Elijah Mossman [1], Anthony Ransford [3], Chris H. Greene [2], Eric R. Hudson [1,4,5], Wesley C. Campbell [1,4,5]

Abstract

We report a theoretical and experimental investigation of autoionizing resonances from the $5d6p\,{}^3\mathrm{D}_1^o$ manifold in neutral barium for efficient loading of ion traps. Our calculations predict large resonant cross sections for many narrow autoionizing resonances, but we find experimentally that for most of these, Doppler broadening during trap loading depresses the effective cross sections that can be achieved in practice. We identify and demonstrate a strong, broad transition at $531\,\mathrm{nm}$, and show that it furnishes an order-of-magnitude increase in trap loading efficiency compared to other demonstrated resonances.

Energy scaling of cold atom-atom-ion three-body recombination

Artjom Krükow, Amir Mohammadi [1], Arne Härter, Johannes Hecker Denschlag [1], Jesús Pérez-Ríos, Chris H. Greene [2]

Abstract

We study three-body recombination of Ba$^+$ + Rb + Rb in the mK regime where a single $^{138}$Ba$^{+}$ ion in a Paul trap is immersed into a cloud of ultracold $^{87}$Rb atoms. We measure the energy dependence of the three-body rate coefficient $k_3$ and compare the results to the theoretical prediction, $k_3 \propto E_{\textrm{col}}^{-3/4}$ where $E_{\textrm{col}}$ is the collision energy. We find agreement if we assume that the non-thermal ion energy distribution is determined by at least two different micro-motion induced energy scales. Furthermore, using classical trajectory calculations we predict how the median binding energy of the formed molecules scales with the collision energy. Our studies give new insights into the kinetics of an ion immersed into an ultracold atom cloud and yield important prospects for atom-ion experiments targeting the s-wave regime.

Resonant structure of low-energy H3+ dissociative recombination

Annemieke Petrignani, Simon Altevogt, Max H. Berg, Dennis Bing, Henrik Buhr [2], Chris H. Greene [5], Manfred Grieser, Jens Hoffmann, Brandon Jordon-Thaden, Viatcheslav Kokoouline [4], Claude Krantz, Holger Kreckel [3], Mario B. Mendes, Oldrich Novotny, Steffen Novotny [1], Dmitry A. Orlov [1], Roland Repnow [1], Tobias Sorg [1], Julia Stuetzel, Andreas Wolf [1]

Abstract

New high-resolution dissociative recombination rate coefficients of rotationally cool and hot H3+ in the vibrational ground state have been measured with a 22-pole trap setup and a Penning ion source, respectively, at the ion storage ring TSR. The experimental results are compared with theoretical calculations to explore the dependence of the rate coefficient on ion temperature and to study the contributions of different symmetries to probe the rich predicted resonance spectrum. The break-up energy was investigated by fragment imaging to derive internal temperatures of the stored parent ions under differing experimental conditions. A systematic experimental assessment of heating effects is performed which, together with a survey of other recent storage-ring data, suggests that the present rotationally cool rate-coefficient measurement was performed at 380^{+50}_{-130} K and that this is the lowest rotational temperature so far realized in storage-ring rate-coefficient measurements on H3+. This partially supports the theoretical suggestion that higher temperatures than assumed in earlier experiments are the main cause for the large gap between the experimental and theoretical rate coefficients. For the rotationally hot rate-coefficient measurement a temperature of below 3250K is derived. From these higher-temperature results it is found that increasing the rotational ion temperature in the calculations cannot fully close the gap between the theoretical and experimental rate coefficients.