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1. Ratchet loading and multi-ensemble operation in an optical lattice clock

   https://doi.org/10.1088/2058-9565/ad6286  

   Hassan, Youssef S; Kobayashi, Takumi; Bothwell, Tobias; Seigel, Jacob L; Hunt, Benjamin D; Beloy, Kyle; Gibble, Kurt; Grogan, Tanner; Ludlow, Andrew D (August 2024, Quantum Science and Technology)

   Abstract We demonstrate programmable control over the spatial distribution of ultra-cold atoms confined in an optical lattice. The control is facilitated through a combination of spatial manipulation of the magneto-optical trap and atomic population shelving to a metastable state. We first employ the technique to load an extended (5 mm) atomic sample with uniform density in an optical lattice clock (OLC), reducing atomic interactions and realizing remarkable frequency homogeneity across the atomic cloud. We also prepare multiple spatially separated atomic ensembles, and realize multi-ensemble clock operation within the standard one-dimensional (1D) OLC architecture. Leveraging this technique, we prepare two oppositely spin-polarized ensembles that are independently addressable, offering a platform for implementing spectroscopic protocols for enhanced tracking of local oscillator phase. Finally, we demonstrate a relative fractional frequency instability at one second of $2.4\left(1\right)\times {10}^{-17}$between two ensembles, useful for characterization of intra-lattice differential systematics. 

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2. Spin-dynamics of pairs of submerged-4f-shell atoms in cylindrically symmetric harmonic traps: connecting multi-channel models to effective analytical approaches

   https://doi.org/10.1088/1367-2630/adc764  

   Li, Hui; Tiesinga, Eite; Li, Ming; Kotochigova, Svetlana (April 2025, New Journal of Physics)

   Abstract We study spin dynamics and quantum magnetism with ultracold highly-magnetic atoms. In particular, we focus on the interactions among rare-earth atoms localized in a site of an optical-lattice potential, modeled as a cylindrically symmetric harmonic oscillator in the presence of a weak external magnetic field. The interactions between the atoms are modeled using a multi-channel Hamiltonian containing multiple spin–spin and anisotropic spin–orbit interactions with strengths that depend on the separation between the atoms. We studied the eigenenergies of the atom pair in a site for different lattice geometries and magnetic field strengths. In parallel, we compared these energies to those found from a simplified approach, where the complex-collisional physics is replaced by a two-length-scale pseudopotential containing the contact and magnetic dipole–dipole interactions. The eigenenergies of this model can be computed analytically within the Born approximation as well as non-perturbatively for strong contact interactions. We have shown that the pseudopotential model can accurately represent the multi-channel Hamiltonian in certain parameter regimes of the shape of the site of an optical lattice. The pseudopotential forms the starting point for many-body, condensed matter simulations involving many atom pairs in different sites of an optical lattice. 

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3. Parallel single-shot measurement and coherent control of solid-state spins below the diffraction limit

   https://doi.org/10.1126/science.abc7821  

   Chen, Songtao; Raha, Mouktik; Phenicie, Christopher M.; Ourari, Salim; Thompson, Jeff D. (October 2020, Science)

   Solid-state spin defects are a promising platform for quantum science and technology. The realization of larger-scale quantum systems with solid-state defects will require high-fidelity control over multiple defects with nanoscale separations, with strong spin-spin interactions for multi-qubit logic operations and the creation of entangled states. We demonstrate an optical frequency-domain multiplexing technique, allowing high-fidelity initialization and single-shot spin measurement of six rare-earth (Er³⁺) ions, within the subwavelength volume of a single, silicon photonic crystal cavity. We also demonstrate subwavelength control over coherent spin rotations by using an optical AC Stark shift. Our approach may be scaled to large numbers of ions with arbitrarily small separation and is a step toward realizing strongly interacting atomic defect ensembles with applications to quantum information processing and fundamental studies of many-body dynamics. 

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4. Discovery of atomic clock-like spin defects in simple oxides from first principles

   https://doi.org/10.1038/s41467-024-49057-8  

   Davidsson, Joel; Onizhuk, Mykyta; Vorwerk, Christian; Galli, Giulia (December 2024, Nature Communications)

   Abstract Virtually noiseless due to the scarcity of spinful nuclei in the lattice, simple oxides hold promise as hosts of solid-state spin qubits. However, no suitable spin defect has yet been found in these systems. Using high-throughput first-principles calculations, we predict spin defects in calcium oxide with electronic properties remarkably similar to those of the NV center in diamond. These defects are charged complexes where a dopant atom — Sb, Bi, or I — occupies the volume vacated by adjacent cation and anion vacancies. The predicted zero phonon line shows that the Bi complex emits in the telecommunication range, and the computed many-body energy levels suggest a viable optical cycle required for qubit initialization. Notably, the high-spin nucleus of each dopant strongly couples to the electron spin, leading to many controllable quantum levels and the emergence of atomic clock-like transitions that are well protected from environmental noise. Specifically, the Hanh-echo coherence time increases beyond seconds at the clock-like transition in the defect with²⁰⁹Bi. Our results pave the way to designing quantum states with long coherence times in simple oxides, making them attractive platforms for quantum technologies. 

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5. Quantum Metrology with a Molecular Lattice Clock and State-Selected Photodissociation of Ultracold Molecules

   Lee, C.-H. (January 2020, Columbia University thesis)

   Over the past few decades, rapid development of laser cooling techniques and narrow-linewidth lasers have allowed atom-based quantum clocks to achieve unprecedented precision. Techniques originally developed for atomic clocks can be extended to ultracold molecules, with applications ranging from quantum-state-controlled ultracold chemistry to searches for new physics. Because of the richness of molecular structure, quantum metrology based on molecules provides possibilities for testing physics that is beyond the scope of traditional atomic clocks. This thesis presents the work performed to establish a state-of-the-art quantum clock based on ultracold molecules. The molecular clock is based on a frequency difference between two vibrational levels in the electronic ground state of 88Sr2 diatomic molecules. Such a clock allows us test molecular QED, improve constraints on nanometer-scale gravity, and potentially provide a model-independent test of temporal variations of the proton-electron mass ratio. Trap-insensitive spectroscopy is crucial for extending coherent molecule-light interactions and achieving a high quality factor Q. We have demonstrated a magic wavelength technique for molecules by manipulating the optical lattice frequency near narrow polarizability resonances. This general technique allows us to increase the coherence time to tens of ms, an improvement of a factor of several thousand, and to narrow the linewidth of a 25 THz vibrational transition initially to 30 Hz. This width corresponds to the quality factor Q = 8 × 10^11. Besides the molecular quantum metrology, investigations of novel phenomena in state-selected photodissociation are also described in this thesis, including magnetic-field control of photodissociation and observation of the crossover from ultracold to quasiclassical chemistry. 

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