Short-lived isomers in Po-192 and Po-194

Isomeric states in Po194 and Po192 were studied at the velocity filter SHIP. The isotopes were produced in the fusion-evaporation reactions Pr141(Fe56, p2n)Po194 and Sm144(V51, p2n)Po192. Several new γ-ray transitions were attributed to the isomers and γ−γ coincidences for both isomers were studied for the first time. The 459-keV transition earlier, tentatively proposed as de-exciting the isomeric level in Po194, was replaced by a new 248-keV transition, and the spin of this isomer was reassigned from (11−) to (10−). The de-excitation of the (11−) isomeric level in Po192 by the 154-keV transition was confirmed and a parallel de-excitation by a 733-keV (E3) transition to (8+) level of the ground-state band was suggested. Moreover, side feeding to the (4+) level of the ground-state band was proposed. The paper also discusses strengths of transitions de-exciting 11− isomers in neighboring Po and Pb isotopes

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

Probing Sizes and Shapes of Nobelium Isotopes by Laser Spectroscopy

Until recently, ground-state nuclear moments of the heaviest nuclei could only be inferred from nuclear spectroscopy, where model assumptions are required. Laser spectroscopy in combination with modern atomic structure calculations is now able to probe these moments directly, in a comprehensive and nuclear-model-independent way. Here we report on unique access to the differential mean-square charge radii of 252, 253, 254No, and therefore to changes in nuclear size and shape. State-of-the-art nuclear density functional calculations describe well the changes in nuclear charge radii in the region of the heavy actinides, indicating an appreciable central depression in the deformed proton density distribution in 252, 254No isotopes. Finally, the hyperfine splitting of 253No was evaluated, enabling a complementary measure of its (quadrupole) deformation, as well as an insight into the neutron single-particle wave function via the nuclear spin and magnetic moment

Fusion reaction 48Ca+249Bk leading to formation of the element Ts (Z=117)

The heaviest currently known nuclei, which have up to 118 protons, have been produced in 48Ca induced reactions with actinide targets. Among them, the element tennessine (Ts), which has 117 protons, has been synthesized by fusing 48Ca with the radioactive target 249Bk, which has a half-life of 327 d. The experiment was performed at the gas-filled recoil separator TASCA. Two long and two short α decay chains were observed. The long chains were attributed to the decay of 294Ts. The possible origin of the short-decay chains is discussed in comparison with the known experimental data. They are found to fit with the decay chain patterns attributed to 293Ts. The present experimental results confirm the previous findings at the Dubna Gas-Filled Recoil Separator on the decay chains originating from the nuclei assigned to Ts

Levels in Th-223 populated by alpha decay of U-227

Levels in 223Th populated by the α decay of 227U were investigated using α−γ decay spectroscopy. The 227U isotope was produced in the fusion-evaporation reaction 22Ne+208Pb at the velocity filter separator for heavy-ion reaction products at Gesellschaft für Schwerionenforschung in Darmstadt (Germany). Several new excited levels and γ transitions were identified in 223Th. An improved α-decay scheme of 227U was suggested. The experimental α-decay energy spectrum of 227U was compared with the Monte Carlo simulation performed using the toolkit geant4.status: publishe

Investigation of electron capture decay of (258)Db and decay of (258)Rf

Electron capture decay of 258 Db was measured directly via delayed coincidences between K X-rays and/or conversion electrons (from the electron capture decay), and spontaneous fission or α decay of the daughter nuclide 258Rf. Delayed K X-rays were also measured in prompt coincidence with conversion electrons, showing that electron capture decay also populates excited levels in the daughter nucleus. Our data indicate electron capture decay from two states in 258Db, thus supporting the existence of two long-lived states in 258Db with some seconds half-life already known from α-decay studies. The analysis of correlations between photons, conversion electrons and fission events resulted in a strong evidence for population of two isomeric states in 258Rf by the electron capture decay of 258Db, with half-lives of T1/2=(15±10) μs and T1/2=(2.4+2.4−0.8) ms. A previously reported α branch of 258Rf was confirmed. However, we obtained a significantly lower branching ratio bα=(0.049±0.016). The technique is discussed as a possible new method for Z-identification of odd-odd superheavy nuclei.status: publishe

Isomeric states in 255Rf, 256Rf and 257Rf

status: publishe

Towards optical spectroscopy of the element nobelium (Z=102) in a buffer gas cell - First on-line experiments on Yb-155 at the velocity filter SHIP with a novel ion collection and atom re-evaporation method of high efficiency

For the investigation of the atomic level structure of heavy elements which can only be produced at on-line facilities such as GSI, a novel experimental procedure has been developed. It is based on Radiation Detected Resonance Ionization Spectroscopy (RADRIS) and can be applied to elements like nobelium produced at rates of a few ions per second. Fusion reaction products are separated from the primary beam by the velocity filter SHIP at GSI, stopped in a buffer gas cell, collected on a tantalum filament and then re-evaporated as atoms. The ions produced by resonance ionization with tunable laser beams are detected via their characteristic α decay. First on-line experiments on α-active 155Yb, which is supposed to have an atomic level structure similar to nobelium, were performed. These test experiments focused on the optimization of the collection and re-evaporation process of the radioactive ions, the laser ionization efficiency and the detection via α decay. An overall efficiency for RADRIS of 0.8% with respect to the target production rate was measured. While further improvements of this efficiency are in progress it should already be sufficient for the search for atomic levels in nobelium.status: publishe