arXiv subjects

Dominik Studer

Publications and source records attributed to Dominik Studer.

7 recordsLinked to original sources

arXiv2026

Measurement of the O$^{-}$ Photodetachment cross-section in the electrostatic storage ring FLSR

The achievable precision of photodetachment studies via tunable laser light has been investigated on circulating oxygen anions at the room-temperature electrostatic low-energy storage ring of Frankfurt University (FLSR) in preparation of investigations on molecular species. For this purpose, the FLSR, originally designed for reaction dynamics studies on positive ions, was upgraded by a source for anions, by the installation of a tunable high repetition rate laser system and by implementation of a transversal interaction region between laser and ion beam. Results on the electron affinity and the ground state fine structure of O$^{-}$, which both serve as a calibration standard, are discussed, exhibiting the performance and accuracy of this new spectroscopic application of the FLSR.

physics.atom-ph↗

arXiv2026

Laser Spectroscopy of Thulium Isotopes Near the (N=82) Shell Closure: Nuclear Moment and Charge Radius of ${}^{152\mathrm{m}}\mathrm{Tm}$

We report on resonance ionization laser spectroscopy measurements performed on both neutron-deficient and neutron-rich thulium ($\mathrm{Tm}, Z=69$) isotopes. Isotope shifts were determined for three atomic ground-state transitions at wavelengths of $389.8\,\mathrm{nm}$, $388.4\,\mathrm{nm}$, and $388.8\,\mathrm{nm}$ in the isotopes ${}^{152\mathrm{m}}\mathrm{Tm}$, ${}^{153}\mathrm{Tm}$, ${}^{154\mathrm{m}}\mathrm{Tm}$, and ${}^{169}\mathrm{Tm}$. In addition, for the $389.8\,\mathrm{nm}$ transition, measurements were extended to the isotope ${}^{170}\mathrm{Tm}$, and the hyperfine structure was partially resolved for all five isotopes. For this transition, the isotope shift could be determined for one more isotope, ${}^{154\mathrm{m}}\mathrm{Tm}$. From the extracted hyperfine coupling constants, the nuclear magnetic dipole moment for ${}^{152\mathrm{m}}\mathrm{Tm}$ was determined for the first time, resulting in $\mu\left({}^{152\mathrm{m}}\mathrm{Tm}\right) = 5.8(3) \mu_\mathrm{N}$. Furthermore, the mean-square nuclear charge radius $\delta\langle r^2\rangle^{152\mathrm{m},169} = -1.86(25)\,\mathrm{fm}^2$ for ${}^{152\mathrm{m}}\mathrm{Tm}$ was extracted from the measured isotope shifts.

nucl-ex↗

arXiv2022

High-resolution laser system for the S3-Low Energy Branch

In this paper we present the first high-resolution laser spectroscopy results obtained at the GISELE laser laboratory of the GANIL-SPIRAL2 facility, in preparation for the first experiments with the S$^3$-Low Energy Branch. Studies of neutron-deficient radioactive isotopes of erbium and tin represent the first physics cases to be studied at S$^3$. The measured isotope-shift and hyperfine structure data are presented for stable isotopes of these elements. The erbium isotopes were studied using the $4f^{12}6s^2$ $^3H_6 \rightarrow 4f^{12}(^3 H)6s6p$ $J = 5$ atomic transition (415 nm) and the tin isotopes were studied by the $5s^25p^2 (^3P_0) \rightarrow 5s^25p6s (^3P_1)$ atomic transition (286.4 nm), and are used as a benchmark of the laser setup. Additionally, the tin isotopes were studied by the $5s^25p6s (^3P_1) \rightarrow 5s^25p6p (^3P_2)$ atomic transition (811.6 nm), for which new isotope-shift data was obtained and the corresponding field-shift $F_{812}$ and mass-shift $M_{812}$ factors are presented.

nucl-ex↗

arXiv2020

Detection of missing low-lying atomic states in actinium

Two lowest-energy odd-parity atomic levels of actinium, 7s^27p 2P^o_1/2, 7s^27p 2P^o_3/2, were observed via two-step resonant laser-ionization spectroscopy and their respective energies were measured to be 7477.36(4) cm^-1 and 12 276.59(2) cm^-1. The lifetimes of these states were determined as 668(11) ns and 255(7) ns, respectively. In addition, these properties were calculated using a hybrid approach that combines configuration interaction and coupled-cluster methods in good agreement. The data are of relevance for understanding the complex atomic spectra of actinides and for developing efficient laser-cooling and ionization schemes for actinium, with possible applications for high-purity medicalisotope production and future fundamental physics experiments with this atom.

physics.atom-ph↗

arXiv2020

The electron affinity of astatine

One of the most important properties influencing the chemical behavior of an element is the energy released with the addition of an extra electron to the neutral atom, referred to as the electron affinity (EA). Among the remaining elements with unknown EA is astatine, the purely radioactive element 85. Astatine is the heaviest naturally occurring halogen and its isotope $^{211}$At is remarkably well suited for targeted radionuclide therapy of cancer. With the At$^-$ anion being involved in many aspects of current astatine labelling protocols, the knowledge of the electron affinity of this element is of prime importance. In addition, the EA can be used to deduce other concepts such as the electronegativity, thereby further improving the understanding of astatine's chemistry. Here, we report the first measurement of the EA for astatine to be 2.41578(7)eV. This result is compared to state-of-the-art relativistic quantum mechanical calculations, which require incorporation of the electron-electron correlation effects on the highest possible level. The developed technique of laser-photodetachment spectroscopy of radioisotopes opens the path for future EA measurements of other radioelements such as polonium, and eventually super-heavy elements, which are produced at a one-atom-at-a-time rate.

physics.atom-ph↗

arXiv2018

Laser spectroscopy of the 1001nm ground state transition in dysprosium

We present the first direct excitation of the presumably ultra-narrow $1001 \, \textrm{nm}$ ground state transition in atomic dysproium. By using resonance ionization spectroscopy with pulsed Ti:sapphire lasers at a hot cavity laser ion source, we were able to measure the isotopic shifts in the $1001 \, \textrm{nm}$ line between all seven stable isotopes. Furthermore, we determined the upper level energy from the atomic transition frequency of the $^{164} \textrm{Dy}$ isotope as $9991.004(1) \, \textrm{cm}^{-1}$ and confirm the level energy listed in the NIST database. Since a sufficiently narrow natural linewidth is an essential prerequisite for high precision spectroscopic investigations for fundamental questions we furthermore determined a lower limit of $2.9(1) \, μ\textrm{s}$ for the lifetime of the excited state.

physics.atom-ph↗

arXiv2017

Efficient and robust photo-ionization loading of beryllium ions

We demonstrate the efficient generation of Be$^+$ ions with a 60 ns and 150 nJ laser pulse near 235 nm for two-step photo-ionization, proven by subsequent counting the number of ions loaded into a linear Paul trap. The bandwidth and power of the laser pulse are chosen in such a way that a first, resonant step fully saturates the entire velocity distribution of beryllium atoms effusing from a thermal oven. The second excitation step is driven by the same light field causing efficient non-resonant ionization. Our ion-loading scheme is more than 15 times more efficient as compared to former pathways using two-photon continuous wave laser excitation.

physics.atom-ph↗