Identification and Control of Electron-Nuclear Spin Defects in Diamond.

We experimentally demonstrate an approach to scale up quantum devices by harnessing spin defects in the environment of a quantum probe. We follow this approach to identify, locate, and control two electron-nuclear spin defects in the environment of a single nitrogen-vacancy center in diamond. By performing spectroscopy at various orientations of the magnetic field, we extract the unknown parameters of the hyperfine and dipolar interaction tensors, which we use to locate the two spin defects and design control sequences to initialize, manipulate, and readout their quantum state. Finally, we create quantum coherence among the three electron spins, paving the way for the creation of genuine tripartite entanglement. This approach will be useful in assembling multispin quantum registers for applications in quantum sensing and quantum information processing.

2000-Times Repeated Imaging of Strontium Atoms in Clock-Magic Tweezer Arrays.

We demonstrate single-atom resolved imaging with a survival probability of 0.99932(8) and a fidelity of 0.99991(1), enabling us to perform repeated high-fidelity imaging of single atoms in tweezers thousands of times. We further observe lifetimes under laser cooling of more than seven minutes, an order of magnitude longer than in previous tweezer studies. Experiments are performed with strontium atoms in 813.4 nm tweezer arrays, which is at a magic wavelength for the clock transition. Tuning to this wavelength is enabled by off-magic Sisyphus cooling on the intercombination line, which lets us choose the tweezer wavelength almost arbitrarily. We find that a single not retroreflected cooling beam in the radial direction is sufficient for mitigating recoil heating during imaging. Moreover, this cooling technique yields temperatures below 5 µK, as measured by release and recapture. Finally, we demonstrate clock-state resolved detection with average survival probability of 0.996(1) and average state detection fidelity of 0.981(1). Our work paves the way for atom-by-atom assembly of large defect-free arrays of alkaline-earth atoms, in which repeated interrogation of the clock transition is an imminent possibility.

Temperature calibration formula for activated charcoal radon collectors.

Radon adsorption by activated charcoal collectors such as PicoRad radon detectors is known to be largely affected by temperature and relative humidity. Quantitative models are, however, still needed for accurate radon estimation in a variable environment. Here we introduce a temperature calibration formula based on the gas adsorption theory to evaluate the radon concentration in air from the average temperature, collection time, and liquid scintillation count rate. On the basis of calibration experiments done by using the 25 m³ radon chamber available at the National Institute of Radiological Sciences in Japan, we found that the radon adsorption efficiency may vary up to a factor of two for temperatures typical of indoor conditions. We expect our results to be useful for establishing standardized protocols for optimized radon assessment in dwellings and workplaces.