Precision Measurement of the First Ionization Potential of Nobelium.

One of the most important atomic properties governing an element's chemical behavior is the energy required to remove its least-bound electron, referred to as the first ionization potential. For the heaviest elements, this fundamental quantity is strongly influenced by relativistic effects which lead to unique chemical properties. Laser spectroscopy on an atom-at-a-time scale was developed and applied to probe the optical spectrum of neutral nobelium near the ionization threshold. The first ionization potential of nobelium is determined here with a very high precision from the convergence of measured Rydberg series to be 6.626 21±0.000 05 eV. This work provides a stringent benchmark for state-of-the-art many-body atomic modeling that considers relativistic and quantum electrodynamic effects and paves the way for high-precision measurements of atomic properties of elements only available from heavy-ion accelerator facilities.

Phase-imaging ion-cyclotron-resonance measurements for short-lived nuclides.

A novel approach based on the projection of the Penning-trap ion motion onto a position-sensitive detector opens the door to very accurate mass measurements on the ppb level even for short-lived nuclides with half-lives well below a second. In addition to the accuracy boost, the new method provides a superior resolving power by which low-lying isomeric states with excitation energy on the 10-keV level can be easily separated from the ground state. A measurement of the mass difference of ^{130}Xe and ^{129}Xe has demonstrated the great potential of the new approach.

Direct mapping of nuclear shell effects in the heaviest elements.

Quantum-mechanical shell effects are expected to strongly enhance nuclear binding on an "island of stability" of superheavy elements. The predicted center at proton number Z = 114, 120, or 126 and neutron number N = 184 has been substantiated by the recent synthesis of new elements up to Z = 118. However, the location of the center and the extension of the island of stability remain vague. High-precision mass spectrometry allows the direct measurement of nuclear binding energies and thus the determination of the strength of shell effects. Here, we present such measurements for nobelium and lawrencium isotopes, which also pin down the deformed shell gap at N = 152.

Octupolar-excitation Penning-trap mass spectrometry for Q-value measurement of double-electron capture in (164)Er.

The theory of octupolar-excitation ion-cyclotron-resonance mass spectrometry is presented which predicts an increase of up to several orders of magnitude in resolving power under certain conditions. The new method has been applied for a direct Penning-trap mass-ratio determination of the (164)Er-(164)Dy mass doublet. (164)Er is a candidate for the search for neutrinoless double-electron capture. However, the measured Q(ϵϵ) value of 25.07(12) keV results in a half-life of 10(30) years for a 1 eV Majorana-neutrino mass.

Resonant enhancement of neutrinoless double-electron capture in 152Gd.

In the search for the nuclide with the largest probability for neutrinoless double-electron capture, we have determined the Q(ϵϵ) value between the ground states of (152)Gd and (152)Sm by Penning-trap mass-ratio measurements. The new Q(ϵϵ) value of 55.70(18) keV results in a half-life of 10(26) yr for a 1 eV neutrino mass. With this smallest half-life among known 0νϵϵ transitions, (152)Gd is a promising candidate for the search for neutrinoless double-electron capture.

Direct mass measurements above uranium bridge the gap to the island of stability.

The mass of an atom incorporates all its constituents and their interactions. The difference between the mass of an atom and the sum of its building blocks (the binding energy) is a manifestation of Einstein's famous relation E = mc(2). The binding energy determines the energy available for nuclear reactions and decays (and thus the creation of elements by stellar nucleosynthesis), and holds the key to the fundamental question of how heavy the elements can be. Superheavy elements have been observed in challenging production experiments, but our present knowledge of the binding energy of these nuclides is based only on the detection of their decay products. The reconstruction from extended decay chains introduces uncertainties that render the interpretation difficult. Here we report direct mass measurements of trans-uranium nuclides. Located at the farthest tip of the actinide species on the proton number-neutron number diagram, these nuclides represent the gateway to the predicted island of stability. In particular, we have determined the mass values of (252-254)No (atomic number 102) with the Penning trap mass spectrometer SHIPTRAP. The uncertainties are of the order of 10 keV/c(2) (representing a relative precision of 0.05 p.p.m.), despite minute production rates of less than one atom per second. Our experiments advance direct mass measurements by ten atomic numbers with no loss in accuracy, and provide reliable anchor points en route to the island of stability.