EPJ Web of Conferences
Volume 34, 2012From Quantum Chemistry to Astrophysics: A Tribute to Pierre Valiron
|Number of page(s)||3|
|Section||Atomic and molecular physics|
|Published online||04 October 2012|
Antiprotonic helium atomcules
Department of Microelectronics and Information Technology, Royal Institute of Technology (KTH), Electrum 229, SE-16440 Kista, Sweden
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About 3% of antiprotons () stopped in helium are long-lived with microsecond lifetimes, against picoseconds in all other materials. This unusual longevity has been ascribed to the trapping of on metastable bound states in He+ helium atom-molecules thus named atomcules. Apart from their unique dual structure investigated by laser spectroscopy – a near-circular quasi-classical Rydberg atom with l ~ n – 1 ~ 37 or a special diatomic molecule with a negatively charged nucleus in high rotational state with J = l – the chemical physics aspects of their interaction with other atoms or molecules constitute an interesting topic for molecular physics. While atomcules may resist to million collisions in helium, molecular contaminants such as H2 are likely to destroy them in a single one, down to very low temperatures. In the Born-Oppenheimer framework, we interpret the molecular interaction obtained by ab initio quantum chemical calculations in terms of classical reactive channels, with activation barriers accounting for the experiments carried out in He and H2. From classical trajectory Monte Carlo simulations, we show that the thermalization stage strongly quenches initial populations, thus reduced to a recovered 3 % trapping fraction. This work illustrates the pertinence of chemical physics concepts to the study of exotic processes involving antimatter. New insights into the physico-chemistry of cold interstellar radicals are anticipated.
© Owned by the authors, published by EDP Sciences, 2012
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