Atom-at-a-time laser resonance ionization spectroscopy of nobelium

Abstract : Optical spectroscopy of a primordial isotope has traditionally formed the basis for understanding the atomic structure of an element. Such studies have been conducted for most elements1 and theoretical modelling can be performed to high precision2, 3, taking into account relativistic effects that scale approximately as the square of the atomic number. However, for the transfermium elements (those with atomic numbers greater than 100), the atomic structure is experimentally unknown. These radioactive elements are produced in nuclear fusion reactions at rates of only a few atoms per second at most and must be studied immediately following their production4, which has so far precluded their optical spectroscopy. Here we report laser resonance ionization spectroscopy of nobelium (No; atomic number 102) in single-atom-at-a-time quantities, in which we identify the ground-state transition 1S0 1P1. By combining this result with data from an observed Rydberg series, we obtain an upper limit for the ionization potential of nobelium. These accurate results from direct laser excitations of outer-shell electrons cannot be achieved using state-of-the-art relativistic many-body calculations5, 6, 7, 8 that include quantum electrodynamic effects, owing to large uncertainties in the modelled transition energies of the complex systems under consideration. Our work opens the door to high-precision measurements of various atomic and nuclear properties of elements heavier than nobelium, and motivates future theoretical work.
Type de document :
Article dans une revue
Nature, Nature Publishing Group, 2016, 538 (7626), pp.495 - 498. 〈10.1038/nature19345〉
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http://hal.in2p3.fr/in2p3-01399898
Contributeur : Michel Lion <>
Soumis le : lundi 21 novembre 2016 - 10:30:47
Dernière modification le : jeudi 1 février 2018 - 01:33:38

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M. Laatiaoui, W. Lauth, H. Backe, M. Block, D. Ackermann, et al.. Atom-at-a-time laser resonance ionization spectroscopy of nobelium. Nature, Nature Publishing Group, 2016, 538 (7626), pp.495 - 498. 〈10.1038/nature19345〉. 〈in2p3-01399898〉

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