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We demonstrate a method of imaging spatially varying magnetic fields using a thin layer of nitrogen-vacancy (NV) centers at the surface of a diamond chip. Fluorescence emitted by the two-dimensional NV ensemble is detected by a CCD array, from which a vector magnetic field pattern is reconstructed. As a demonstration, ac current is passed through wires placed on the diamond chip surface, and the resulting ac magnetic field patterns are imaged using an echo-based technique with sub-micron resolution over a \(140 \mu m\) x \(140 \mu m\) field of view, giving single-pixel sensitivity \(\sim 100 nT / \sqrt{Hz}\). We discuss ongoing efforts to further improve the sensitivity, as well as potential bioimaging applications such as real-time imaging of activity in functional, cultured networks of neurons., Engineering and Applied Sciences, Physics, Other Research Unit

We describe a method to enhance the sensitivity of precision measurements that takes advantage of the environment of a quantum sensor to amplify the response of the sensor to weak external perturbations. An individual qubit is used to sense the dynamics of surrounding ancillary qubits, which are in turn affected by the external field to be measured. The resulting sensitivity enhancement is determined by the number of ancillas that are coupled strongly to the sensor qubit; it does not depend on the exact values of the coupling strengths and is resilient to many forms of decoherence. The method achieves nearly Heisenberg-limited precision measurement, using a novel class of entangled states. We discuss specific applications to improve clock sensitivity using trapped ions and magnetic sensing based on electronic spins in diamond., Physics

We present an experimental and theoretical study of electronic spin decoherence in ensembles of nitrogen-vacancy (NV) color centers in bulk high-purity diamond at room temperature. Under appropriate conditions, we find ensemble NV spin coherence times (\(T_2\)) comparable to that of single NV with \(T_2>600 \mu s\) for a sample with natural abundance of \(^{13}\)C and paramagnetic impurity density ∼1015 cm\(^{−3}\). We also observe a sharp decrease in the coherence time with misalignment of the static magnetic field relative to the NV electronic spin axis, consistent with theoretical modeling of NV coupling to a \(^{13}\)C nuclear-spin bath. The long coherence times and increased signal-to-noise provided by room-temperature NV ensembles will aid many applications of NV centers in precision magnetometry and quantum information., Engineering and Applied Sciences, Physics, Other Research Unit

We consider a protocol for the control of few-qubit registers comprising one electronic spin embedded in a nuclear spin bath. We show how to isolate a few proximal nuclear spins from the rest of the bath and use them as building blocks for a potentially scalable quantum information processor. We describe how coherent control techniques based on magnetic resonance methods can be adapted to these solid-state spin systems, to provide not only efficient, high fidelity manipulation but also decoupling from the spin bath. As an example, we analyze feasible performances and practical limitations in the realistic setting of nitrogen-vacancy centers in diamond., Physics

We investigate the coherence properties of individual nuclear spin quantum bits in diamond [Dutt et al., Science, 316, 1312 (2007)] when a proximal electronic spin associated with a nitrogen-vacancy (NV) center is being interrogated by optical radiation. The resulting nuclear spin dynamics are governed by time-dependent hyperfine interaction associated with rapid electronic transitions, which can be described by a spin-fluctuator model. We show that due to a process analogous to motional averaging in nuclear magnetic resonance, the nuclear spin coherence can be preserved after a large number of optical excitation cycles. Our theoretical analysis is in good agreement with experimental results. It indicates a novel approach that could potentially isolate the nuclear spin system completely from the electronic environment., Physics

Periodically driven (Floquet) quantum systems have recently been a focus of nonequilibrium physics by virtue of their rich dynamics. Time-periodic systems not only exhibit symmetries that resemble those in spatially periodic systems, but also display novel behavior that arises from symmetry breaking. Characterization of such dynamical symmetries is crucial, but often challenging due to limited driving strength and lack of an experimentally accessible characterization technique. Here, we show how to reveal dynamical symmetries, namely, parity, rotation, and particle-hole symmetries, by observing symmetry-induced Floquet selection rules. Notably, we exploit modulated driving to reach the strong light-matter coupling regime, and we introduce a protocol to experimentally extract the transition matrix elements between Floquet states from the system coherent evolution. By using nitrogen-vacancy centers in diamond as an experimental test bed, we execute our protocol to observe symmetry-protected dark states and dark bands, and coherent destruction of tunneling. Our work shows how one can exploit the quantum control toolkit to study dynamical symmetries that arise in the topological phases of strongly driven Floquet systems. [ABSTRACT FROM AUTHOR]

Characterizing out-of-equilibrium many-body dynamics is a complex but crucial task for quantum applications and understanding fundamental phenomena. A central question is the role of localization in quenching thermalization in many-body systems and whether such localization survives in the presence of interactions. Probing this question in real systems necessitates the development of an experimentally measurable metric that can distinguish between different types of localization. While it is known that the localized phase of interacting systems [many-body localization (MBL)] exhibits a long-time logarithmic growth in entanglement entropy that distinguishes it from the noninteracting case of Anderson localization (AL), entanglement entropy is difficult to measure experimentally. Here, we present a novel correlation metric, capable of distinguishing MBL from AL in high-temperature spin systems. We demonstrate the use of this metric to detect localization in a natural solid-state spin system using nuclear magnetic resonance (NMR). We engineer the natural Hamiltonian to controllably introduce disorder and interactions, and observe the emergence of localization. In particular, while our correlation metric saturates for AL, it slowly keeps increasing for MBL, demonstrating analogous features to entanglement entropy, as we show in simulations. Our results show that our NMR techniques, akin to measuring out-of-time correlations, are well suited for studying localization in spin systems. [ABSTRACT FROM AUTHOR]

Precise characterization of a system's Hamiltonian is crucial to its high-fidelity control that would enable many quantum technologies, ranging from quantum computation to communication and sensing. In particular, nonsecular parts of the Hamiltonian are usually more difficult to characterize, even if they can give rise to subtle but non-negligible effects. Here we present a strategy for the precise estimation of the transverse hyperfine coupling between an electronic and a nuclear spin, exploiting effects due to nominally forbidden transitions during the Rabi nutation of the nuclear spin. We applied the method to precisely determine the transverse coupling between a nitrogen-vacancy center electronic spin and its nitrogen nuclear spin. In addition, we show how this transverse hyperfine coupling, which has been often neglected in experiments, is crucial to achieving large enhancements of the nuclear Rabi nutation rate. [ABSTRACT FROM AUTHOR]

How a many-body quantum system thermalizes--or fails to do so--under its own interaction is a fundamental yet elusive concept. Here we demonstrate nuclear magnetic resonance observation of the emergence of prethermalization by measuring out-of-time ordered correlations. We exploit Hamiltonian engineering techniques to tune the strength of spin-spin interactions and of a transverse magnetic field in a spin chain system, as well as to invert the Hamiltonian sign to reveal out-of-time ordered correlations. At large fields, we observe an emergent conserved quantity due to prethermalization, which can be revealed by an early saturation of correlations. Our experiment not only demonstrates a new protocol to measure out-of-time ordered correlations, but also provides new insights in the study of quantum thermodynamics. [ABSTRACT FROM AUTHOR]

The field of nanoscale magnetic resonance imaging (NanoMRI) was started 30 years ago. It was motivated by the desire to image single molecules and molecular assemblies, such as proteins and virus particles, with near-atomic spatial resolution and on a length scale of 100 nm. Over the years, the NanoMRI field has also expanded to include the goal of useful high-resolution nuclear magnetic resonance (NMR) spectroscopy of molecules under ambient conditions, including samples up to the micron-scale. The realization of these goals requires the development of spin detection techniques that are many orders of magnitude more sensitive than conventional NMR and MRI, capable of detecting and controlling nanoscale ensembles of spins. Over the years, a number of different technical approaches to NanoMRI have emerged, each possessing a distinct set of capabilities for basic and applied areas of science. The goal of this roadmap article is to report the current state of the art in NanoMRI technologies, outline the areas where they are poised to have impact, identify the challenges that lie ahead, and propose methods to meet these challenges. This roadmap also shows how developments in NanoMRI techniques can lead to breakthroughs in emerging quantum science and technology applications., (Creative Commons Attribution license.)

Recent advances in engineering and control of nanoscale quantum sensors have opened new paradigms in precision metrology. Unfortunately, hardware restrictions often limit the sensor performance. In nanoscale magnetic resonance probes, for instance, finite sampling times greatly limit the achievable sensitivity and spectral resolution. Here we introduce a technique for coherent quantum interpolation that can overcome these problems. Using a quantum sensor associated with the nitrogen vacancy center in diamond, we experimentally demonstrate that quantum interpolation can achieve spectroscopy of classical magnetic fields and individual quantum spins with orders of magnitude finer frequency resolution than conventionally possible. Not only is quantum interpolation an enabling technique to extract structural and chemical information from single biomolecules, but it can be directly applied to other quantum systems for superresolution quantum spectroscopy.