Gabriella Kripkó-Koncz

Linear radio-frequency quadrupole (RFQ) traps are crucial for ion and phase-space manipulation across diverse physics platforms, including quantum information processing, precision atomic spectroscopy, and high-resolution mass or laser spectrometry. We present the design, electrostatic field optimization, and performance characterization of a scalable, multi-layer printed circuit board (PCB) linear RFQ trap. By utilizing a PCB-based "stacked-electrode" geometry to generate high-quality quadrupolar fields, this architecture suppresses higher-order multipole field components by up to an order of magnitude compared to planar "flat surface-electrode" designs and allows for reclaiming up to 60% of the radial pseudopotential-well depth of an ideal hyperbolic quadrupole. Following a thorough optimisation and characterization using both simulations and experiments, we demonstrate its suitability as a cooler buncher, showing rapid helium buffer-gas cooling with time constants between 34 +/- 3 us and 412 +/- 23 us, and achieving a highly compressed longitudinal phase-space emittance of only 58 +/- 4 eV*ns. The low beam emittance provides flexible control of the extracted bunch properties: weak extraction fields yield energy spreads down to 2.5 +/- 0.4 eV, whereas strong fields produce ultra-narrow temporal widths down to 2.6 +/- 0.3 ns. The results establish our PCB-RFQ platform as a versatile, scalable, and cost-effective alternative to traditionally machined rod-based RFQ assemblies for advanced ion-trapping, beam-preparation, or quantum applications.

Molecules have proven to be sensitive tools for studying physics beyond the standard model, with heavy and deformed nuclei offering decisive sensitivity to parity- and time-reversal-violating effects. However, almost all elements beyond lead, occupying the 6p~to~5f atomic orbitals, lack stable isotopes, hence molecules containing them are referred to as radioactive molecules. Among those, radium monofluoride has seen particular interest, but to date, research on radioactive molecules has mainly been limited to large-scale nuclear facilities. Here, we present a scheme that allows efficient and fast harvest of radioactive ions (including short-lived Ra), and show ion gas-phase reaction studies of singly and doubly charged Ra, Po, and Pb ions with SF$_6$ gas inside an ion trap. Our results show that the chemical reaction rate of Ra$^+$ is in line with trends of other alkaline earth elements, further support by quantum chemical computations. The reaction Ra$^{2+}$ + SF$_6$ $\rightarrow$ RaF${^+}$ + SF$_5^{+}$ achieves an almost unity conversion efficiency, making it particularly suitable for the application for studies in physics beyond the standard model. The scheme enables future decentralized research avenues with short-lived radioactive molecules for fundamental physics research at laboratories without the need for local nuclear reactors or accelerators.