David R. Leibrandt

Integrated photonics in trapped-ion systems are critical for the realization of applications such as portable optical atomic clocks and scalable quantum computers. However, system-level integration of all required functionalities remains a key challenge. In this work, we demonstrate an autonomously operating optical clock having a short-term frequency instability of $3.14(5)\times 10^{-14} / \sqrtτ$ using an ensemble of four $^{171}\textrm{Yb}^{+}$ ions trapped in a multi-site surface-electrode trap at room temperature. All clock operations are performed with light delivered via on-chip waveguides. We showcase the system's resilience through sustained, autonomous operation featuring automated ion shuttling and reloading to mitigate ion loss during interleaved clock measurements. This work paves the way beyond component-level functionality to establish a viable and robust architecture for the next generation of portable, multi-ion quantum sensors and computers.

We report a single-ion optical atomic clock with fractional frequency uncertainty of $5.5\times10^{-19}$ and fractional frequency stability of $3.5 \times10^{-16}/\sqrt{τ/\mathrm{s}}$, based on quantum logic spectroscopy of a single $^{27}$Al$^+$ ion. A co-trapped $^{25}$Mg$^+$ ion provides sympathetic cooling and quantum logic readout of the $^{27}$Al$^+$ $^1$S$_0\leftrightarrow^3$P$_0$ clock transition. A Rabi probe duration of 1 s, enabled by laser stability transfer from a remote cryogenic silicon cavity across a 3.6 km fiber link, results in a threefold reduction in instability compared to previous $^{27}$Al$^+$ clocks. Systematic uncertainties are lower due to an improved ion trap electrical design, which reduces excess micromotion, and a new vacuum system, which reduces collisional shifts. We also perform a direction-sensitive measurement of the ac magnetic field due to the RF ion trap, eliminating systematic uncertainty due to field orientation.

In quantum logic spectroscopy (QLS), one species of trapped ion is used as a sensor to detect the state of an otherwise inaccessible ion species. This extends precision measurements to a broader class of atomic and molecular systems for applications like atomic clocks and tests of fundamental physics. Here, we develop a new technique based on a Schrödinger cat interferometer to address the problem of scaling QLS to larger ion numbers. We demonstrate the basic features of this method using various combinations of $^{25}\text{Mg}^+$ logic ions and $^{27}\text{Al}^+$ spectroscopy ions. We observe higher detection efficiency by increasing the number of $^{25}\text{Mg}^+$ ions. Applied to multiple $^{27}\text{Al}^+$, this method will improve the stability of high-accuracy optical clocks and could enable Heisenberg-limited QLS.

We use quantum-logic spectroscopy (QLS) and interrogate rotational transitions of a single CaH+ ion with a highly coherent frequency comb, achieving a fractional statistical uncertainty for a transition line center of 4 x 10^-13. We also improve the resolution in measurement of the Stark effect due to the radio-frequency (rf) electric field experienced by a molecular ion in an rf Paul trap, which we characterize and model. This allows us to determine the electric dipole moment of CaH+ by systematically displacing the ion to sample different known rf electric fields and measuring the resultant shifts in transition frequency.

We propose a many-ion optical atomic clock based on three-dimensional Coulomb crystals of order one thousand Sn$^{2+}$ ions confined in a linear RF Paul trap. Sn$^{2+}$ has a unique combination of features that is not available in previously considered ions: a $^1$S$_0$ $\leftrightarrow$ $^3$P$_0$ clock transition between two states with zero electronic and nuclear angular momentum (I = J = F = 0) making it immune to nonscalar perturbations, a negative differential polarizability making it possible to operate the trap in a manner such that the two dominant shifts for three-dimensional ion crystals cancel each other, and a laser-accessible transition suitable for direct laser cooling and state readout. We present calculations of the differential polarizability, other relevant atomic properties, and the motion of ions in large Coulomb crystals, in order to estimate the achievable accuracy and precision of Sn$^{2+}$ Coulomb-crystal clocks.

Spectroscopy is a powerful tool for studying molecules and is commonly performed on large thermal molecular ensembles that are perturbed by motional shifts and interactions with the environment and one another, resulting in convoluted spectra and limited resolution. Here, we use generally applicable quantum-logic techniques to prepare a trapped molecular ion in a single quantum state, drive terahertz rotational transitions with an optical frequency comb, and read out the final state non-destructively, leaving the molecule ready for further manipulation. We resolve rotational transitions to 11 significant digits and derive the rotational constant of CaH+ to be B_R = 142501777.9(1.7) kHz. Our approach suits a wide range of molecular ions, including polyatomics and species relevant for tests of fundamental physics, chemistry, and astrophysics.

Laser cooling and trapping of atoms and atomic ions has led to numerous advances including the observation of exotic phases of matter, development of exquisite sensors and state-of-the-art atomic clocks. The same level of control in molecules could also lead to profound developments such as controlled chemical reactions and sensitive probes of fundamental theories, but the vibrational and rotational degrees of freedom in molecules pose a formidable challenge for controlling their quantum mechanical states. Here, we use quantum-logic spectroscopy (QLS) for preparation and nondestructive detection of quantum mechanical states in molecular ions. We develop a general technique to enable optical pumping and preparation of the molecule into a pure initial state. This allows for the observation of high-resolution spectra in a single ion (here CaH+) and coherent phenomena such as Rabi flopping and Ramsey fringes. The protocol requires a single, far-off resonant laser, which is not specific to the molecule, so that many other molecular ions, including polyatomic species, could be treated with the same methods in the same apparatus by changing the molecular source. Combined with long interrogation times afforded by ion traps, a broad range of molecular ions could be studied with unprecedented control and precision, representing a critical step towards proposed applications, such as precision molecular spectroscopy, stringent tests of fundamental physics, quantum computing, and precision control of molecular dynamics.

We report a demonstration and quantitative characterization of one-dimensional cavity cooling of a single trapped 88Sr+ ion in the resolved sideband regime. We measure the spectrum of cavity transitions, the rates of cavity heating and cooling, and the steady-state cooling limit. The cavity cooling dynamics and cooling limit of 22.5(3) motional quanta, limited by the moderate coupling between the ion and the cavity, are consistent with a simple model [Phys. Rev. A 64, 033405] without any free parameters, validating the rate equation model for cavity cooling.

We demonstrate loading by laser ablation of $^{88}$Sr$^+$ ions into a mm-scale surface-electrode ion trap. The laser used for ablation is a pulsed, frequency-tripled Nd:YAG with pulse energies of 1-10 mJ and durations of 3-5 ns. An additional laser is not required to photoionize the ablated material. The efficiency and lifetime of several candidate materials for the laser ablation target are characterized by measuring the trapped ion fluorescence signal for a number of consecutive loads. Additionally, laser ablation is used to load traps with a trap depth (40 meV) below where electron impact ionization loading is typically successful ($\gtrsim$ 500 meV).

We demonstrate a method for loading surface electrode ion traps by electron impact ionization. The method relies on the property of surface electrode geometries that the trap depth can be increased at the cost of more micromotion. By introducing a buffer gas, we can counteract the rf heating assocated with the micromotion and benefit from the larger trap depth. After an initial loading of the trap, standard compensation techniques can be used to cancel the stray fields resulting from charged dielectric and allow for the loading of the trap at ultra-high vacuum.