The in-gas-jet laser spectroscopy method relies on the production of uniform and low-temperature gas jets to fully resolve the atomic hyperfine structure and efficiently determine fundamental nuclear properties of short-lived isotopes from, e.g., the hardly accessible actinide and transactinide elements. In this article we present the studies devoted to designing, producing, and characterizing the flow properties of a convergent-divergent (de Laval) hypersonic nozzle with a superior performance for laser spectroscopy applications. A novel flow mapping technique, based on resonance ionization spectroscopy (RIS), has been employed to characterize the local flow properties of an argon gas jet formed by this nozzle, revealing a 61.5-mm long, highly collimated atomic jet at a uniform low temperature of 16.6(5) K [Mach 8.11(12)] that will enable laser spectroscopy experiments on heavy-exotic nuclei with an unprecedented spectral resolution and a high efficiency. These results have been compared with those obtained by planar laser induced fluorescence spectroscopy (PLIFS) studies and show a good agreement between the two techniques and a significant improvement in efficiency of the RIS mapping method with respect to PLIFS. The data are compared to state-of-the-art fluid-dynamics calculations that were carried out to obtain the nozzle contour and simulate its performance, as well as to explain the observation of a possible onset of argon nucleation.

We present the first results obtained from the S${}^3$ Low-Energy Branch, the gas cell setup at SPIRAL2-GANIL, which will be installed behind the S${}^3$ spectrometer for atomic and nuclear spectroscopy studies of exotic nuclei. The installation is currently being commissioned offline, with the aim to establish optimum conditions for the operation of the radio frequency quadrupole ion guides, mass separation and ion bunching, providing high-efficiency and low-energy spatial spread for the isotopes of interest. Transmission and mass-resolving power measurements are presented for the different components of the S${}^3$-LEB setup. In addition, a single-longitudinal-mode, injection-locked, pumped pulsed-titanium–sapphire laser system has been recently implemented and is used for the first proof-of-principle measurements in an offline laser laboratory. Laser spectroscopy measurements of erbium, which is the commissioning case of the S${}^3$ spectrometer, are presented using the $4f^{12}6s^2$${}^3{H}_6\to 4f^{12}{(}^{3}H)6s6p$ optical transition.

RAdiation-Detected Resonance Ionization Spectroscopy (RADRIS) is a versatile method for highly sensitive laser spectroscopy studies of the heaviest actinides. Most of these nuclides need to be produced at accelerator facilities in fusion-evaporation reactions and are studied immediately after their production and separation from the primary beam due to their short half-lives and low production rates of only a few atoms per second or less. Only recently, the first laser spectroscopic investigation of nobelium ($Z=102$) was performed by applying the RADRIS technique in a buffer-gas-filled stopping cell at the GSI in Darmstadt, Germany. To expand this technique to other nobelium isotopes and for the search for atomic levels in the heaviest actinide element, lawrencium ($Z=103$), the sensitivity of the RADRIS setup needed to be further improved. Therefore, a new movable double-detector setup was developed, which enhances the overall efficiency by approximately 65% compared to the previously used single-detector setup. Further development work was performed to enable the study of longer-lived (t${}_{1/2}>1$ h) and shorter-lived nuclides (t${}_{1/2}<1$ s) with the RADRIS method. With a new rotatable multi-detector design, the long-lived isotope ${}^{254}$Fm (t${}_{1/2}=3.2 \mathrm{h}$) becomes within reach for laser spectroscopy. Upcoming experiments will also tackle the short-lived isotope ${}^{251}$No (t${}_{1/2}=0.8 \mathrm{s}$) by applying a newly implemented short RADRIS measurement cycle.