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arXiv:2604.11743

Sub-nanosecond control for spin-defect quantum memories with a low-cost, compact FPGA platform

Victor Marcenac, Tommy Nguyen, Julie Chen, Weitao He, Enrique Garcia, Yuyang Han, Bethany E. Matthews, Tiamike Dudley, Andrew Mounce, Kai-Mei C. Fu, Maxwell F. Parsons

quant-phSubmitted Apr 13, 2026• Announced Apr 14, 2026• 0 citations
arXivHTMLPDF

Abstract

Dynamical decoupling techniques are widely used to characterize and control the environments of solid-state quantum defects, enabling solid-state quantum memories and nanoscale quantum sensors. However, resolution is often limited by the timing granularity of control hardware, which can undersample narrow spectral features and distort extracted parameters. Here, we demonstrate sub-nanosecond timing control on an inexpensive FPGA-based platform by extending the open-source QICK (Quantum Instrumentation Control Kit) framework using a waveform-offset method. This approach achieves an effective timing resolution of 200~ps on an RF system-on-chip device without modification to the underlying hardware. We apply this capability to dynamical decoupling spectroscopy of nitrogen-vacancy centers in diamond, enabling precise extraction of hyperfine couplings of individual $^{13}\mathrm{C}$ nuclear spins and resolving spectral features that are otherwise undersampled. These results demonstrate that high-resolution, device-level characterization of spin-based quantum memories can be achieved using flexible, inexpensive control hardware, providing a scalable alternative to commercial arbitrary waveform generators.

Comments
15 pages, 4 figures, submitted to QCE26

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Dynamical decoupling techniques are widely used to characterize and control the environments of solid-state quantum defects, enabling solid-state quantum memories and nanoscale quantum sensors. However, resolution is often limited by the timing granularity of control hardware, which can undersample narrow spectral features and distort extracted parameters. Here, we demonstrate sub-nanosecond timing control on an inexpensive FPGA-based platform by extending the open-source QICK (Quantum Instrumentation Control Kit) framework using a waveform-offset method. This approach achieves an effective timing resolution of 200~ps on an RF system-on-chip device without modification to the underlying hardware. We apply this capability to dynamical decoupling spectroscopy of nitrogen-vacancy centers in diamond, enabling precise extraction of hyperfine couplings of individual 13C^{13}\mathrm{C}13C nuclear spins and resolving spectral features that are otherwise undersampled. These results demonstrate that high-resolution, device-level characterization of spin-based quantum memories can be achieved using flexible, inexpensive control hardware, providing a scalable alternative to commercial arbitrary waveform generators.
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Abstract The Nitrogen-Vacancy (NV) defect in diamond is a unique quantum system that offers precision sensing of nanoscale physical quantities at room temperature beyond the current state-of-the-art. The benchmark parameters for nanoscale magnetometry applications are sensitivity, spectral resolution, and dynamic range. Under realistic conditions the NV sensors controlled by conventional sensing schemes suffer from limitations of these parameters. Here we experimentally show a new method called dynamical sensitivity control (DYSCO) that boost the benchmark parameters and thus extends the practical applicability of the NV spin for nanoscale sensing. In contrast to conventional dynamical decoupling schemes, where π pulse trains toggle the spin precession abruptly, the DYSCO method allows for a smooth, analog modulation of the quantum probe’s sensitivity. Our method decouples frequency selectivity and spectral resolution unconstrained over the bandwidth (1.85 MHz–392 Hz in our experiments). Using DYSCO we demonstrate high-accuracy NV magnetometry without |2π| ambiguities, an enhancement of the dynamic range by a factor of 4 · 103, and interrogation times exceeding 2 ms in off-the-shelf diamond. In a broader perspective the DYSCO method provides a handle on the inherent dynamics of quantum systems offering decisive advantages for NV centre based applications notably in quantum information and single molecule NMR/MRI.
Magnetic field fluctuations on nanometer length scales manifest in a diverse range of phenomena -- electron and spin dynamics in materials and devices, quantum many-body systems, and molecular chemistry. Measuring these phenomena requires sensors with a challenging combination of broad spectral bandwidth, high sensitivity, and nanoscale spatial resolution. Nitrogen-vacancy (NV) centers, atom-like quantum sensors in diamond, possess the requisite sensitivity and nanoscale sensing volume, but are typically limited in bandwidth by the practical speed of the applied quantum control sequence. Here, we overcome this limitation by exposing the NV qubit to a microwave dressing field during a dynamical decoupling sequence, which both amplifies and frequency-mixes target signals at arbitrary frequencies into the detection band of the dynamical decoupling protocol. We demonstrate this approach by using NV centers to detect both coherent and noisy nanoscale spin wave dynamics in a magnetic yttrium-iron-garnet (YIG) thin film over a broad frequency range. Our technique generalizes to other qubit platforms, providing a versatile framework for nanoscale spectroscopy across diverse physical and chemical systems.
Abstract 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 (≲ 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°. 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.