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Justin J. Welter

Publications and source records attributed to Justin J. Welter.

2 recordsLinked to original sources

Direct Measurement of the Singlet Lifetime and Photoexcitation Behavior of the Boron Vacancy Center in Hexagonal Boron Nitride

Optically active spin defects in van der Waals (vdW) materials are a promising platform for quantum sensing, potentially enabling shorter standoff distances than defects in diamond and thus improved measurement signal-to-noise ratio (SNR) and spatial resolution. The most studied such defect is the negatively charged boron vacancy center ($V^{-}_{B}$) in hexagonal boron nitride (hBN), yet many of its electronic and spin transition rates and branching ratios remain unknown. Here, we use time-resolved photoluminescence (PL) measurements with a nanosecond rise-time 515 nm laser to directly measure the singlet state lifetime of a $V^{-}_{B}$ ensemble in neutron-irradiated, sub-micron flakes of hBN. We perform this measurement on 16 flakes at room temperature and obtain an average lifetime of 15(3) ns. Additionally, we probe the PL dynamics of thermal and optically polarized electronic spin distributions of the $V^{-}_{B}$ ensemble in a sub-micron hBN flake, and fit our results to a 9-level model to extract electronic transition rates. Lastly, we present PL measurements that potentially indicate optically-induced conversion of $V^{-}_{B}$ to another electronic state, or possibly the neutral charge state ($V^{0}_{B}$), in neutron-irradiated hBN flakes of size $>$ 1 $μ$m.

quant-ph

High-resolution, Wide-frequency-range Magnetic Spectroscopy with Solid-state Spin Ensembles

Quantum systems composed of solid-state electronic spins can be sensitive detectors of narrowband magnetic fields. A prominent example is the nitrogen-vacancy (NV) center in diamond, which has been employed for magnetic spectroscopy with high spatial and spectral resolution. However, NV-diamond spectroscopy protocols are typically based on dynamical decoupling sequences, which are limited to low-frequency signals ($\lesssim{20}\,$MHz) due to the technical requirements on microwave (MW) pulses used to manipulate NV electronic spins. In this work, we experimentally demonstrate a high-resolution magnetic spectroscopy protocol that integrates a quantum frequency mixing (QFM) effect in a dense NV ensemble with coherently averaged synchronized readout (CASR) to provide both a wide range of signal frequency detection and sub-Hz spectral resolution. We assess the sensitivity of this QFM-CASR protocol across a frequency range of 10$\,$MHz to 4$\,$GHz. By measuring the spectra of multi-frequency signals near 0.6, 2.4 and 4$\,$GHz, we demonstrate sub-Hz spectral resolution with a nT-scale noise floor for the target signal, and precise phase measurement with error $<1^\circ$. Compared to state-of-the-art NV-diamond techniques for narrowband magnetic spectroscopy, the QFM-CASR protocol greatly extends the detectable frequency range, enabling applications in high-frequency radio frequency (RF) and MW signal microscopy and analysis, as well as tesla-scale nuclear magnetic resonance (NMR) spectroscopy of small samples.

quant-ph