Quantum sensing uses quantum systems as sensors to capture weak signals and is providing opportunities in science and technology. The biggest challenge in quantum sensing is decoherence due to the coupling between the sensor and the environment. The dissipation will destroy the quantum coherence and reduce the performance of the sensor. Here we show that quantum sensing can be realized under dissipation by engineering the steady state of the sensor. We demonstrate this protocol with a magnetometer based on ensemble nitrogen-vacancy centers in diamond, while neither high-quality initialization or readout of the sensor nor sophisticated dynamical decoupling sequences are required. Thus our method provides a concise and decoherence-resistant means of quantum sensing. The frequency resolution and precision of our magnetometer are far beyond the coherence time of the sensor. Furthermore, we show that the dissipation can be engineered to improve the performance of our sensor. By increasing the laser pumping, magnetic signals in a broad audio-frequency band from dc up to 140 kHz can be tackled by our method. Besides the potential applications in magnetic sensing and imaging on the microscopic scale, our results may provide opportunities for improvement of a variety of high-precision spectroscopies based on other quantum sensors.
Quantum sensing uses quantum systems as sensors to capture weak signals and is providing opportunities in science and technology. The biggest challenge in quantum sensing is decoherence due to the coupling between the sensor and the environment. The dissipation will destroy the quantum coherence and reduce the performance of the sensor. Here we show that quantum sensing can be realized under dissipation by engineering the steady state of the sensor. We demonstrate this protocol with a magnetometer based on ensemble nitrogen-vacancy centers in diamond, while neither high-quality initialization or readout of the sensor nor sophisticated dynamical decoupling sequences are required. Thus our method provides a concise and decoherence-resistant means of quantum sensing. The frequency resolution and precision of our magnetometer are far beyond the coherence time of the sensor. Furthermore, we show that the dissipation can be engineered to improve the performance of our sensor. By increasing the laser pumping, magnetic signals in a broad audio-frequency band from dc up to 140 kHz can be tackled by our method. Besides the potential applications in magnetic sensing and imaging on the microscopic scale, our results may provide opportunities for improvement of a variety of high-precision spectroscopies based on other quantum sensors.
In modern-day quantum metrology, quantum sensors are widely employed to detect weak magnetic fields or nanoscale signals. Quantum devices, exploiting quantum coherence, are inevitably connected to physical constants and can achieve accuracy, repeatability, and precision approaching fundamental limits. As a result, these sensors have shown utility in a wide range of research domains spanning both science and technology. A rapidly emerging quantum sensing platform employs atomic-scale defects in crystals. In particular, magnetometry using nitrogen-vacancy (NV) color centers in diamond has garnered increasing interest. NV systems possess a combination of remarkable properties, optical addressability, long coherence times, and biocompatibility. Sensors based on NV centers excel in spatial resolution and magnetic sensitivity. These diamond-based sensors promise comparable combination of high spatial resolution and magnetic sensitivity without cryogenic operation. The above properties of NV magnetometers promise increasingly integrated quantum measurement technology, as a result, they have been extensively developed with various protocols and find use in numerous applications spanning materials characterization, nuclear magnetic resonance (NMR), condensed matter physics, paleomagnetism, neuroscience and living systems biology, and industrial vector magnetometry. In this chapter, NV centers are explored for magnetic sensing in a number of contexts. In general, we introduce novel regimes for magnetic-field probes with NV ensembles. Specifically, NV centers are developed for sensitive magnetometers for applications where microwaves (MWs) are prohibitively invasive and operations need to be carried out under zero ambient magnetic field. The primary goal of our discussion is to improve the utility of these NV center-based magnetometers.
Quantum sensing with solid-state spins offers the promise of high spatial resolution, bandwidth, and dynamic range at sensitivities comparable to more mature quantum sensing technologies, such as atomic vapor cells and superconducting devices. However, despite comparable theoretical sensitivity limits, the performance of bulk solid-state quantum sensors has so far lagged behind these more mature alternatives. A recent review [Barry et al., Rev. Mod. Phys. 92, 015004 (2020)] suggests several paths to improve performance of magnetometers employing nitrogen-vacancy defects in diamond, the most-studied solid-state quantum sensing platform. Implementing several suggested techniques, we demonstrate the most sensitive nitrogen-vacancy-based bulk magnetometer reported to date. Our approach combines tailored diamond growth to achieve low strain and long intrinsic dephasing times, the use of double-quantum Ramsey and Hahn-echo magnetometry sequences for broadband and narrowband magnetometry, respectively, and P1 driving to further extend dephasing time. Notably, the device does not include a flux concentrator, preserving the fixed response of the nitrogen vacancies to magnetic field. The magnetometer realizes a minimum sensitivity of 460fTs1/2 in a broadband dc-sensitive mode and 210fTs1/2 in a narrowband ac mode. We describe the experimental setup in detail and highlight potential paths for future improvement.
Magnetic sensing and imaging instruments are important tools in biological and material sciences. There is an increasing demand for attaining higher sensitivity and spatial resolution, with implementations using a single qubit offering potential improvements in both directions. In this article we describe a scanning magnetometer based on the nitrogen-vacancy center in diamond as the sensor. By means of a quantum-assisted readout scheme together with advances in photon collection efficiency, our device exhibits an enhancement in signal to noise ratio of close to an order of magnitude compared to the standard fluorescence readout of the nitrogen-vacancy center. This is demonstrated by comparing non-assisted and assisted methods in a T1 relaxation time measurement.
Magnetic sensing and imaging instruments are important tools in biological and material sciences. There is an increasing demand for attaining higher sensitivity and spatial resolution, with implementations using a single qubit offering potential improvements in both directions. In this article we describe a scanning magnetometer based on the nitrogen-vacancy center in diamond as the sensor. By means of a quantum-assisted readout scheme together with advances in photon collection efficiency, our device exhibits an enhancement in signal to noise ratio of close to an order of magnitude compared to the standard fluorescence readout of the nitrogen-vacancy center. This is demonstrated by comparing non-assisted and assisted methods in a T1 relaxation time measurement.
Quantum sensors encompass a diverse class of devices that exploit quantum coherence to detect weak or nanoscale signals. As their behavior is tied to physical constants, quantum sensors can achieve accuracy, repeatability, and precision approaching fundamental limits [1, 2]. As a result, these sensors have shown utility in a wide range of applications in both science and engineering leading to innovations. Among many solid-state spin systems, nitrogen-vacancy (NV) centers in diamonds have attracted considerable attention as a leading platform in many fields of quantum technologies, from quantum sensing to information processing and communication applications. They have superior physical properties, and their quantum coherence is preserved even at room temperature. The energy levels of NV centers are sensitive to magnetic fields, electric fields, strain, and temperature, and the spatial resolution is scalable from nanometers to millimeters. Therefore, diamond quantum sensors are distinctive sensors with multimodality and span scalable application fields. To realize an ideal quantum sensor for applications, the technical challenges in the sensor materials and the quantum control techniques, such as coherent microwave spin manipulation, effective optical spin-state initialization, and readout, have been developed. This chapter briefly explains the sensing principle using NV centers and then introduces sensor systems for biomedical applications, and monitoring of batteries for electric vehicles and internal power devices.
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.