Quantum-enhanced sensing with spin-bearing defects in solids is important for measuring magnetic fields at the atomic scale, but progress is impeded by the difficulty of accessing ensembles of strongly coupled spins that can be entangled deterministically. This study exploits an optically dark electronic-nuclear spin defect near a single nitrogen-vacancy center in diamond to create an entangled state of two electronic spins, and measure the amplitude of time-varying magnetic fields with superior performance. With their stability under optical illumination, dark electronic spins can be repeatedly measured through the N-$V$ center to further improve the signal-to-noise ratio.
Quantum-enhanced sensing with spin-bearing defects in solids is important for measuring magnetic fields at the atomic scale, but progress is impeded by the difficulty of accessing ensembles of strongly coupled spins that can be entangled deterministically. This study exploits an optically dark electronic-nuclear spin defect near a single nitrogen-vacancy center in diamond to create an entangled state of two electronic spins, and measure the amplitude of time-varying magnetic fields with superior performance. With their stability under optical illumination, dark electronic spins can be repeatedly measured through the N-V center to further improve the signal-to-noise ratio.
A promising approach for multi-qubit quantum registers is to use optically addressable spins to control multiple dark electron-spin defects in the environment. While recent experiments have observed signatures of coherent interactions with such dark spins, it is an open challenge to realize the individual control required for quantum information processing. Here, we demonstrate the heralded initialisation, control and entanglement of individual dark spins associated to multiple P1 centers, which are part of a spin bath surrounding a nitrogen-vacancy center in diamond. We realize projective measurements to prepare the multiple degrees of freedom of P1 centers-their Jahn-Teller axis, nuclear spin and charge state-and exploit these to selectively access multiple P1s in the bath. We develop control and single-shot readout of the nuclear and electron spin, and use this to demonstrate an entangled state of two P1 centers. These results provide a proof-of-principle towards using dark electron-nuclear spin defects as qubits for quantum sensing, computation and networks.
The performance of solid-state quantum sensors based on electronic spin defects is often limited by the presence of environmental spin impurities that cause decoherence. A promising approach to improve these quantum sensors is to convert environment spins into useful resources for sensing, in particular, entangled states. However, the sensitivity enhancement that can be achieved from entangled states is limited by experimental constraints, such as control errors, decoherence, and time overheads. Here we experimentally demonstrate the efficient use of an unknown electronic spin defect in the proximity of a nitrogen-vacancy center in diamond to achieve both an entangled quantum sensor and a quantum memory for readout. We show that, whereas entanglement alone does not provide an enhancement in sensitivity, combining both entanglement and repetitive readout achieves an enhancement in performance over the use of a single-spin sensor, and more broadly we discuss regimes where sensitivity could be enhanced. Our results critically highlight the challenges in improving quantum sensors using entangled states of electronic spins, while providing an important benchmark in the quest for entanglement-assisted metrology.
Abstract Quantum sensing exploits the strong sensitivity of quantum systems to measure small external signals. The nitrogen-vacancy (NV) center in diamond is one of the most promising platforms for real-world quantum sensing applications, predominantly used as a magnetometer. However, its magnetic field sensitivity vanishes when a bias magnetic field acts perpendicular to the NV axis. Here, we introduce a different sensing strategy assisted by the nitrogen nuclear spin that uses the entanglement between the electron and nuclear spins to restore the magnetic field sensitivity. This, in turn, allows us to detect small changes in the magnetic field angle relative to the NV axis. Furthermore, based on the same underlying principle, we show that the NV coupling strength to magnetic noise, and hence its coherence time, exhibits a strong asymmetric angle dependence. This allows us to uncover the directional properties of the local magnetic environment and to realize maximal decoupling from anisotropic noise.
Nitrogen-vacancy centers in diamond are sensitive probes of time-varying magnetic fields that can be used to identify unknown spin defects in their nearby environment. Performing spectral quantum measurements on such single quantum probes enables gaining information about the internal structure and dynamics of nearby spin defects that would otherwise be inaccessible through direct or indirect measurements with classical probes. Here, we identify a system composed of two electron-nuclear spin defects in a diamond crystal by performing a series of spectral identification measurements using a single nitrogen-vacancy center in diamond. Besides enabling the identification of new spin defects and studies of their formation mechanisms, these techniques will be useful for scaling up quantum systems by converting environmental spin defects into quantum resources.
The ability to measure and manipulate the quantum state of a single spin in a solid state system opens up a broad range of powerful applications ranging from nano probes to quantum information processing. Over the past few years, a number of ground breaking experiments have been conducted on paramagnetic nitrogen vacancy defect centers in diamond, including up to 3-qubit entanglement, single-shot-readout of a nuclear spin, selective access of two coupled centers and magnetic, electric and thermographic sensing at the nanoscale with promising properties in some cases exceeding most currently known techniques. Yet, almost all of the experiments conducted so far focus on centers deeply buried in the diamond, which is undesirable especially for sensing applications, but also in terms of scalability and electronic access to the information. In this work we focus on the spin physics of centers only few nanometers below the surface, where the unique properties of the center are strongly influenced by the external environment. We coherently manipulated and detected single spins at ambient temperature by combining optically detected magnetic resonance with single molecule spectroscopy using a confocal microscope. We measured the spin dephasing behavior and the phase relaxation time and examined the primary sources of decoherence. Furthermore, we observed effects of water, atmosphere and paramagnetic molecules on the coherence and readability of spins in nanodiamonds and demonstrated ways to preserve the coherence using external magnetic fields and a number of different dynamic decoupling pulse sequences. In addition, we measured couplings to proximal nuclear spins by continuous wave spectroscopy and to molecules on the surface by double electron electron resonance. Also, we demonstrate execution of the refined Deutsch-Jozsa algorithm on a nitrogen vacancy center in a nanodiamond. Finally, we propose new technological approach for realtime measurements of magnetic fields using a single spin in diamond. In test measurements using external fields and spatially resolved measurements of the field from a magnetic microwire a sensitivity of a few uT / sqrt(Hz) was achieved.
Quantum sensing has witnessed rapid development and transition from laboratories to practical applications in the past decade. Applications of quantum sensors, ranging from nanotechnologies to biosensing, are expected to benefit from quantum sensors' unprecedented spatial resolution and sensitivity. Solid-state spin systems are particularly attractive platforms for quantum sensing technologies because room temperature operation is viable while reaching the quantum limits of sensitivity. Among various solid-state spin systems, nitrogen-vacancy (NV) centers in diamond demonstrated high-fidelity initialization, coherent control, and high contrast readout of the electron spin state. However, electron spin coherence due to noise from the surrounding spin bath and this environment effect limits the sensitivity of NV centers. Thus, a critical task in NV center-based quantum sensing is sensitivity enhancement through coherence protection. Several strategies, such as dynamical decoupling techniques, feedback control, and nuclear spin-assisted sensing protocols, have been developed and realized for this task. Among these strategies, nuclear spin-assisted protocols have demonstrated greater enhancement of electron spin coherence. In addition, the electron and nuclear spin pair of an NV center in diamond naturally allows the application of the nuclear spin-assisted sensitivity enhancement protocol. Owing to long nuclear coherence times, further enhancement of sensitivity can be achieved by exploiting active nuclear spins (e.g., 14N, 13C) in the proximity of an NV center as memory ancillas when coupled with the NV center. Here, we review the spin properties of NV centers, mechanisms of the nuclear spin-assisted protocol and its gate variation, and the status of quantum sensing applications in high-resolution nuclear spin spectroscopy, atomic imaging, and magnetic field sensing. We discuss the potential for commercialization, current challenges in sensitivity enhancement, and conclude with future research directions for promoting the development of nuclear spin-assisted protocol and its integration into industrial applications.