Nitrogen-vacancy (NV) centers in nanodiamonds have emerged as a promising quantum sensing platform for biomedical imaging applications, yet random orientations of individual particles present significant challenges in large-scale sensor calibration. In this study, we demonstrate a novel approach to simultaneously determine each particle's crystallographic axes and the surrounding local vector magnetic field. Specifically, a minimum of four distinct bias fields is required to unambiguously extract both the orientation and the local field. We validate our method experimentally using NV centers in two scenarios: (1) in a bulk diamond with known crystal orientation as a proof of concept, and (2) on various single nanodiamonds to mimic real-world applications. Our work represents a crucial step towards unlocking the full potential of nanodiamonds for advanced applications such as in-situ biomedical imaging and nanoscale sensing in complex environments.
Nitrogen-vacancy (NV) centers in nanodiamonds have emerged as a promising quantum sensing platform for biomedical imaging applications, yet random orientations of individual particles present significant challenges in large-scale sensor calibration. In this study, we demonstrate a novel approach to simultaneously determine each particle's crystallographic axes and the surrounding local vector magnetic field. Specifically, a minimum of four distinct bias fields is required to unambiguously extract both the orientation and the local field. We validate our method experimentally using NV centers in two scenarios: (1) in a bulk diamond with known crystal orientation as a proof of concept, and (2) on various single nanodiamonds to mimic real-world applications. Our work represents a crucial step towards unlocking the full potential of nanodiamonds for advanced applications such as in-situ biomedical imaging and nanoscale sensing in complex environments.
Nitrogen-vacancy (NV) centers in bulk diamond, as an excellent spin-based vector quantum sensor, require precise determination of the axis orientation information. Here, we efficiently visualize and completely determine the NV axis orientation in bulk diamond, assisted by a radially polarized beam. We observe the rotational asymmetric fluorescence pattern of NV centers in bulk diamond, which is quite different from that in nanodiamonds. Our theoretical calculations show this difference is mainly due to the fact that the ratio between the longitudinal and transverse electric field components of the focused radially polarized beam is greatly weakened in bulk diamond. This fluorescence pattern asymmetry can uniquely determine both the azimuth angle and the polar angle without degeneracy in bulk diamond. Then, we verify these theories in bulk diamond with different orientations and nanodiamonds. The experimental result is consistent with that of the traditional method by measuring a series of optically detected magnetic resonance (ODMR) spectra, and the error is less than 3.0 degrees. Our method can be easily extended to other solid-state spin systems and shows great potential in quantum sensing of vector magnetic fields and nanoscale dynamic processes.
Individual, scannable nitrogen vacancy (NV) centers in single crystal diamond nanostructures enable nanoscale, quantitative imaging of magnetic stray fields. Nevertheless, important parameters like distance between the NV center and the sample and the orientation of the NV high symmetry axis are often not known precisely and enter data evaluation as free fitting parameters. We here use scanning NV imaging on micro-patterned, perpendicularly magnetized stripes and discs. From these measurements, we directly infer NV - sample distance d_NV and the NV's azimuthal orientation without the need for an external vector magnet control. We determine d_NV = 31.5 nm, while we infer the azimuthal orientation with a precision of 3°. We additionally employ commercially available silicon needles to image the apex topography of our diamond nanostructures to detect surface contamination. Simultaneously, monitoring NV fluorescence as a function of the needle's position allows us to estimate the lateral placement of the NV inside the diamond nanostructure.
Nitrogen-vacancy (NV) centers in diamond provide a solid-state platform for quantum sensing. While optically detected magnetic resonance techniques offer high sensitivity, their reliance on microwaves introduces heating and stray electromagnetic fields that can perturb nearby samples. Optical approaches based on cross-relaxation between differently oriented NV centers remove this constraint but have so far required stringent alignment of the external field with crystallographic axes, restricting their practicality. Here we introduce a general framework for microwave-free vector magnetometry at near-zero field that leverages Bayesian inference to extract both the magnetic field vector and the NV orientation directly from photoluminescence maps. An analytical model of cross-relaxation resonances enables efficient inference under arbitrary field and orientation configurations, while naturally incorporating the discrete degeneracies of the NV symmetry. We experimentally demonstrate robust orientation determination and vector-field reconstruction, establishing a general route toward compact and alignment-free NV magnetometers for practical sensing applications.
Quantum sensors based on nitrogen vacancy (NV) centers in diamond have been a central topic in the sensing community for more than a decade. The extraordinary properties at room temperature of the spin system in diamond have made it one of the most prominent quantum platforms for the development of commercial quantum sensors. In particular, the sensitivity of the electronic spin in NV centers has made diamond-based magnetic sensors of special interest for their potential application in medical, industrial or navigation solutions. However, the use of these sensors for universal vector magnetometry was constrained by the need for previous knowledge on the field being measured to fully exploit their benefits. In this work, we show a method to perform unconditional vector magnetometry without the need of external information on the magnetic field, based only on the spatial arrangement of the diamond and the microwave antenna combination. While previous NV-based vector magnetometry methods require partial knowledge of the magnetic field (e.g. a calibrated bias field), we exploit the possibilities of selecting particular directions of the spins in the diamond with elliptically polarized microwave fields. We prove that our method allows to estimate both magnitude and direction of external magnetic fields without further assumptions or constraints.
Abstract Powered by the mutual developments in instrumentation, materials and theoretical descriptions, sensing and imaging capabilities of quantum emitters in solids have significantly increased in the past two decades. Quantum emitters in solids, whose properties resemble those of atoms and ions, provide alternative ways to probing natural and artificial nanoscopic systems with minimum disturbance and ultimate spatial resolution. Among those emerging quantum emitters, the nitrogen vacancy (NV) color center in diamond is an outstanding example due to its intrinsic properties at room temperature (highly-luminescent, photo-stable, biocompatible, highly-coherent spin states). This review article summarizes recent advances and achievements in using NV centers within nano- and single crystal diamonds in sensing and imaging. We also highlight prevalent challenges and material aspects for different types of diamond and outline the main parameters to consider when using color centers as sensors. As a novel sensing resource, we highlight the properties of NV centers as light emitting electrical dipoles and their coupling to other nanoscale dipoles e.g. graphene.
The recent decade has witnessed exciting developments in quantum science and technology. Quantum sensing is a rapidly growing branch, which exploits the fragility of quantum systems to detect small external signals. The extreme control at the single-atom level and the remarkably long coherence time of engineered quantum systems enable unprecedented sensitivity and precision, beating the performance of classical techniques. The nitrogen-vacancy (NV) center in diamond is one of the most promising quantum sensors. Its unique advantages have attracted considerable attention, including a long spin coherence time throughout a broad temperature range, nanoscale resolution limited by the sensor-sample distance, convenient optical control of its spin states and remarkably versatile sensing capabilities. Its properties are well studied under a bias magnetic field oriented along its quantization axis. However, its sensing capabilities in the presence of an off-axis magnetic field are much less explored. My research aims to unlock the full potential of NV quantum sensor by developing new sensing modalities under a magnetic field acting perpendicular to the NV axis, and furthermore, integrating them into a scanning probe microscope. In this dissertation, I will report our progress toward building a scanning NV multimodal quantum imaging platform, which will open up exciting opportunities in measuring nanoscale phenomena. The first chapter provides an introduction to the background of quantum sensing with NV centers, followed by a discussion on its basic properties and established sensing techniques. The second and third chapters are dedicated to two experiments performed under a perpendicular magnetic field where traditional NV magnetometry based on the Zeeman effect fails. In the second chapter, I will introduce a new sensing strategy that uses the entanglement between the electron and nuclear spins to restore the magnetic field sensitivity under this unfavored condition. This allows us to sense small changes in the magnetic field angle relative to the NV axis, and to detect anisotropic magnetic noise in the local environment. In the third chapter, I will present our latest development of scanning NV electrometry, where a single NV at the apex of a diamond scanning probe images external alternating (AC) and direct (DC) electric fields with sub-100 nm resolution. In the last chapter, I will discuss our efforts on four experiments that were left unfinished. I will present the results we have achieved, analyze the challenges that we faced and propose potential solutions to overcome them.