John M. Gray

We report precision measurements of the ratio of Landé $g$ factors between the $3^2D_{5/2}$ and $4^2S_{1/2}$ states of a single trapped $^{40}\text{Ca}^+$ ion. The measurements are performed in two distinct ion trap apparatus: a cryogenic surface electrode radiofrequency Paul trap and a room-temperature permanent magnet Penning trap. The Penning trap measurements yield a ratio of $0.599~488~813~3(2)$, which represents a more than 40-fold uncertainty reduction compared to previous work. The radiofrequency trap measurement yields a concurring value of $0.599~488~813(6)$. We estimate that systematic shifts for each system are well below the respective statistical uncertainty.

The trapped-ion quantum charge-coupled device (QCCD) architecture is a leading candidate for advanced quantum information processing. In current QCCD implementations, imperfect ion transport and anomalous heating can excite ion motion during a calculation. To counteract this, intermediate cooling is necessary to maintain high-fidelity gate performance. Cooling the computational ions sympathetically with ions of another species, a commonly employed strategy, creates a significant runtime bottleneck. Here, we demonstrate a different approach we call exchange cooling. Unlike sympathetic cooling, exchange cooling does not require trapping two different atomic species. The protocol introduces a bank of "coolant" ions which are repeatedly laser cooled. A computational ion can then be cooled by transporting a coolant ion into its proximity. We test this concept experimentally with two $^{40}\mathrm{Ca}^{+}$ ions, executing the necessary transport in 107 $\mathrm{μs}$, an order of magnitude faster than typical sympathetic cooling durations. We remove over 96%, and as many as 102(5) quanta, of axial motional energy from the computational ion. We verify that re-cooling the coolant ion does not decohere the computational ion. This approach validates the feasibility of a single-species QCCD processor, capable of fast quantum simulation and computation.

Trapping cold, chemically important molecules with electromagnetic fields is a useful technique to study small molecules and their interactions. Traps provide long interaction times that are needed to precisely examine these low density molecular samples. However, the trapping fields lead to non-uniform molecular density distributions in these systems. Therefore, it is important to be able to experimentally characterize the spatial density distribution in the trap. Ionizing molecules in different locations in the trap using resonance enhanced multiphoton ionization (REMPI) and detecting the resulting ions can be used to probe the density distribution even with the low density present in these experiments because of the extremely high efficiency of detection. Until recently, one of the most chemically important molecules, OH, did not have a convenient REMPI scheme. Here, we use a newly developed 1 + 1' REMPI scheme to detect trapped cold OH molecules. We use this capability to measure trap dynamics of the central density of the cloud and the density distribution. These types of measurements can be used to optimize loading of molecules into traps, as well as to help characterize the energy distribution, which is critical knowledge for interpreting molecular collision experiments.

We demonstrate sympathetic sideband cooling of a $^{40}$CaH$^{+}$ molecular ion co-trapped with a $^{40}$Ca$^{+}$ atomic ion in a linear Paul trap. Both axial modes of the two-ion chain are simultaneously cooled to near the ground state of motion. The center of mass mode is cooled to an average quanta of harmonic motion $\overline{n}_{\mathrm{COM}} = 0.13 \pm 0.03$, corresponding to a temperature of $12.47 \pm 0.03 ~μ$K. The breathing mode is cooled to $\overline{n}_{\mathrm{BM}} = 0.05 \pm 0.02$, corresponding to a temperature of $15.36 \pm 0.01~μ$K.