arXiv subjects

Addison Hartman

Publications and source records attributed to Addison Hartman.

3 recordsLinked to original sources

arXiv2026

Experimental realization of a rotating radio-frequency ion trap for precision metrology

We discuss the experimental realization of the rotating radio-frequency (rrf) trap, proposed by Hasegawa and Bollinger [Phys. Rev. A 72, 043403 (2005)]. Compared to a traditional linear rf (lrf) Paul trap, the rrf trap is a closer analogy to the popular mechanical lecture demonstration for a Paul trap. In an ion trap with reslistic, non-ideal electrode geometry, the rrf trap averages over angular variations in the effective potential. This averaging provides more uniform confinement and reduces ion loss at equal confinement strength compared with the lrf trap. This feature makes the rrf trap configuration advantageous for precision metrology application, such as electron electric dipole moment (eEDM) measurements.

physics.atom-ph↗

arXiv2025

High-Efficiency Quantum-State Detection of ThF$^+$ with Resonance-Enhanced Multiphoton Asymmetric Dissociation

Efficient quantum-state detection is crucial for many precision control experiments, such as the ongoing effort to probe the electron's electric dipole moment using trapped molecular $^{232}\mathrm{ThF}^+$ ions at JILA. While quantum state detection through state-selective photodissociation has been successfully implemented on this molecule, progress has been hindered by low dissociation efficiency. In this work, we perform spectroscopy on the molecule to identify excited states that facilitate more efficient photodissociation. For the most favorable transition, we achieve a dissociation efficiency of 57(14)% with quantum state selectivity. Additionally, we discuss several state detection protocols that leverage favorable excited states that will facilitate simultaneous readout of all EDM relevant states, allowing further improvement of overall statistics.

physics.atom-ph↗

arXiv2024

State Selective Preparation and Nondestructive Detection of Trapped ${\rm O}_2^+$

The ability to prepare molecular ions in selected quantum states enables studies in areas such as chemistry, metrology, spectroscopy, quantum information, and precision measurements. Here, we demonstrate $(2+1)$ resonance-enhanced multiphoton ionization (REMPI) of oxygen, both in a molecular beam and in an ion trap. The two-photon transition in the REMPI spectrum is rotationally resolved, allowing ionization from a selected rovibrational state of O$_2$. Fits to this spectrum determine spectroscopic parameters of the O$_2$ $d\,^1\Pi_g$ state and resolve a discrepancy in the literature regarding its band origin. The trapped molecular ions are cooled by co-trapped atomic ions. Fluorescence mass spectrometry nondestructively demonstrates the presence of the photoionized O$_2^+$. We discuss strategies for maximizing the fraction of ions produced in the ground rovibrational state. For $(2+1)$ REMPI through the $d\,^1\Pi_g$ state, we show that the Q(1) transition is preferred for neutral O$_2$ at rotational temperatures below 50~K, while the O(3) transition is more suitable at higher temperatures. The combination of state-selective loading and nondestructive detection of trapped molecular ions has applications in optical clocks, tests of fundamental physics, and control of chemical reactions.

physics.chem-ph↗