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Physics Letters B

Laser-controlled production of Rydberg positronium via charge exchange collisions

Andrew J. Speck, C. H. Storry, Eric A. Hessels, G. Gabrielse

Published Aug 5, 2004• 28 citations
Publisher

Abstract

Lasers are used to choose the binding energies of highly excited positronium atoms (Ps*) created via charge exchange collisions. The lasers directly excite cesium (Cs) atoms to highly excited states (Cs*). These large Cs*atoms have a large cross section for resonant charge exchange collisions with trapped positrons. Highly excited Ps* is formed with a binding energy that is determined by the initial laser excitation. These Ps* should have a large cross section for resonant charge exchange collisions with trapped antiprotons—suggesting a possible new way to produce cold antihydrogen.

DOI
10.1016/j.physletb.2004.07.044

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Lasers are used to choose the binding energies of highly excited positronium atoms (Ps*) created via charge exchange collisions. The lasers directly excite cesium (Cs) atoms to highly excited states (Cs*). These large Csatoms have a large cross section for resonant charge exchange collisions with trapped positrons. Highly excited Ps is formed with a binding energy that is determined by the initial laser excitation. These Ps* should have a large cross section for resonant charge exchange collisions with trapped antiprotons—suggesting a possible new way to produce cold antihydrogen.
Abstract Lasers are used to control the production of highly excited positronium atoms (Ps*). The laser light excites Cs atoms to Rydberg states that have a large cross section for resonant charge-exchange collisions with cold trapped positrons. For each trial with 30 million trapped positrons, more than 700 000 of the created Ps* have trajectories near the axis of the apparatus, and are detected using Stark ionization. This number of Ps* is 500 times higher than realized in an earlier proof-of-principle demonstration (2004 Phys. Lett. B 597 257). A second charge exchange of these near-axis Ps* with trapped antiprotons could be used to produce cold antihydrogen, and this antihydrogen production is expected to be increased by a similar factor.
Laser-controlled charge exchange is a promising method for producing cold antihydrogen. Caesium atoms in Rydberg states collide with positrons and create positronium. These positronium atoms then interact with antiprotons, forming antihydrogen. Laser excitation of the caesium atoms is essential to increase the cross section of the charge-exchange collisions. This method was demonstrated in 2004 by the ATRAP collaboration by using an available copper vapour laser. For a second generation of charge-exchange experiments we have designed a new semiconductor laser system that features several improvements compared to the copper vapour laser. We describe this new laser system and show the results from the excitation of caesium atoms to Rydberg states within the strong magnetic fields in the ATRAP apparatus.
Our ATRAP collaboration has now demonstrated a second technique for antihydrogen (H̄) production. Lasers are used for the first time to control the production of H̄ atoms in our cryogenic apparatus at CERN. As suggested in ref. [2] and first reported in ref. [1], lasers excite a thermal beam of cesium (Cs) atoms to a Rydberg state. In a first charge exchange collision one of these laser‐excited Cs atoms (Cs*) and a cold e+ produces positronium (Ps). Our measurements at Harvard([3]) and at CERN([1]) confirm CTMC simulations([2]) that the laser‐selected binding energy in the Cs atom is preserved by the collision and results in Ps with the selected binding energy. A second charge exchange is between one of these Ps atoms and a trapped p̄ . H̄ is produced by this second collision and is expected to again have the same binding energy. One advantage of this technique as discussed in ref. [2] is that the H̄ produced is expected to be extremely cold, at the temperature of the trapped p̄ , allowing for possible confinement of the H̄ atoms in a magnetic trap.
Lasers are used for the first time to control the production of antihydrogen (H ). Sequential, resonant charge exchange collisions are involved in a method that is very different than the only other method used so far-producing slow H during positron cooling of antiprotons in a nested Penning trap. Two attractive features are that the laser frequencies determine the H binding energy, and that the production of extremely cold H should be possible in principle-likely close to what is needed for confinement in a trap, as needed for precise laser spectroscopy.
An efficient method for production of cold antihydrogen $(\mathrm{H}\ifmmode\bar\else\textasciimacron\fi{})$ is proposed. Alkali-metal atoms laser excited to a Rydberg state are charge exchanged with cold trapped positrons, producing Rydberg states of positronium. In a second Rydberg-state charge exchange, the positronium atoms give up their Rydberg positrons to cold trapped antiprotons, producing Rydberg states of $\mathrm{H}\ifmmode\bar\else\textasciimacron\fi{}$. These $\mathrm{H}\ifmmode\bar\else\textasciimacron\fi{}$ atoms soon decay down to the ground state, and, because they are cold, could be trapped in a magnetic trap. The efficiency of the process results from the extremely large cross sections for Rydberg charge exchange. Classical trajectory Monte Carlo calculations indicate an $\mathrm{H}\ifmmode\bar\else\textasciimacron\fi{}$ instantaneous production rate of 106/{}^{6}/6/s.
Antihydrogen production by charge exchange reaction between positronium (Ps) atoms and antiprotons requires an efficient excitation of Ps atoms up to high-nnn levels (Rydberg levels). In this study it is assumed that a Ps cloud is produced within a relatively strong uniform magnetic field (1T)(1\phantom{\rule{0.3em}{0ex}}\mathrm{T})(1T) and with a relatively high temperature (100K)(100\phantom{\rule{0.3em}{0ex}}\mathrm{K})(100K). Consequently, the structure of energy levels are deeply modified by Zeeman and motional Stark effects. A two-step laser light excitation, the first one from ground to n=3n=3n=3 and the second from this level to a Rydberg level, is proposed and the physics of the problem is discussed. We derive a simple formula giving the absorption probability with substantially incoherent laser pulses. A 30% population deposition in high-nnn states can be reached with feasible lasers suitably tailored in power and spectral bandwidth.