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arXiv:2609.16106

Direct Observation of Dipolar-Driven Anisotropic Quantum Projection Noise in a Solid-State Spin Ensemble

Tasuku Ono, Weijie Wu, Haopu Yang, Lillian B. Hughes Wyatt, Benjamin Brenner, Che Liu, Collin Fan, Chris R. Laumann, Jonathan N. Hallén, Emily J. Davis, Ania C. Bleszynski Jayich, Norman Y. Yao

quant-phcond-mat.dis-nncond-mat.mes-hallcond-mat.stat-mechSubmitted Sep 14, 2026• Announced Sep 16, 2026• 0 citations
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Abstract

The nitrogen-vacancy (NV) center in diamond is a prominent quantum-sensing platform. Combining readout at the quantum projection noise limit with strong dipolar interactions promises substantial gains in sensitivity. However, experimentally accessing this regime has remained a longstanding challenge. In this work, we demonstrate quantum-projection-noise-resolved readout of a strongly-interacting, two-dimensional ensemble of NV centers. Our approach leverages repetitive readout via the NV's intrinsic $^{15}$N nuclear memory at a moderate magnetic field ($\sim 0.3$ T), improving the readout fidelities by nearly an order of magnitude. This enables us to directly resolve the quantum projection noise of a coherent spin state and to watch the ensemble's intrinsic dipolar interactions shear this noise into an anisotropic profile. Our results open the door to direct measurements of spin squeezing and entanglement-enhanced sensing in the solid state.

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The nitrogen-vacancy (NV) center in diamond is a prominent quantum-sensing platform. Combining readout at the quantum projection noise limit with strong dipolar interactions promises substantial gains in sensitivity. However, experimentally accessing this regime has remained a longstanding challenge. In this work, we demonstrate quantum-projection-noise-resolved readout of a strongly-interacting, two-dimensional ensemble of NV centers. Our approach leverages repetitive readout via the NV's intrinsic 15^{15}15N nuclear memory at a moderate magnetic field (∼0.3\sim 0.3∼0.3 T), improving the readout fidelities by nearly an order of magnitude. This enables us to directly resolve the quantum projection noise of a coherent spin state and to watch the ensemble's intrinsic dipolar interactions shear this noise into an anisotropic profile. Our results open the door to direct measurements of spin squeezing and entanglement-enhanced sensing in the solid state.
Abstract Spin ensembles are central to quantum science, from fundamental physics searches to magnetic resonance spectroscopy and quantum sensing. The standard quantum limit for their performance is ultimately posed by spin projection noise, yet solid-state implementations have so far been limited by significantly larger photon shot noise. Here, we demonstrate a direct quantum non-demolition readout of a mesoscopic ensemble of nitrogen-vacancy (NV) centers in diamond that surpasses the photon shot-noise limit and approaches the intrinsic spin projection noise. By stabilizing the intrinsic 14 N nuclear spin bath at high magnetic fields and employing a repetitive nuclear-assisted spin readout, we achieve a noise reduction of 3.8 dB below the thermal projection noise level. This enables direct access to the intrinsic fluctuations of the spin ensemble, allowing us to directly observe the signatures of correlated spin states. Our results establish projection noise-limited readout as a practical tool for solid-state quantum sensors, opening pathways to quantum-enhanced metrology, direct detection of many-body correlations, and the implementation of spin squeezing in mesoscopic solid-state ensembles.
Solid-state spin ensembles have emerged as a leading platform for micro- and nanoscale sensing, combining high sensitivity, nanoscale spatial resolution, and operation under ambient conditions. At high spin densities, magnetic dipole–dipole interactions typically limit sensing performance by reducing coherence, but can in principle be harnessed to enhance sensitivity. Realizing such interaction-enhanced sensing in practice, however, remains challenging due to the intrinsic anisotropy of dipolar interactions and the random spatial distribution of spins. This thesis presents a series of experimental works that culminate in a practical interaction-enhanced magnetometer based on ensembles of nitrogen-vacancy (NV) centers in diamond. Our approach is based on collective, one-axis-twisting-like (OAT-like) dynamics engineered from native dipolar interactions using controlled nanoscale spin textures, in combination with a dressed-state qubit encoding that significantly extends the sensor coherence time. These results open the door to practical deployment of interaction-enhanced quantum sensors for nanoscale biological imaging and material characterization.
Many-body dynamics constitutes a promising approach for creating correlations between quantum particles which can be used for applications in sensing and metrology. However, utilizing this potential for substantial gains in practical settings is a challenging task with only a very few applications realized to date. Here, we demonstrate an approach to nanoscale magnetic sensing enabled by strongly interacting electronic spins in a room temperature solid. By coherently controlling collective many-body dynamics of a dipolar ensemble of ∼104\sim 10^4∼104 nitrogen-vacancy (NV) centres in diamond with pulsed magnetic field gradients, we demonstrate practical metrological gain up to 7.9(2) dB7.9(2)\,\mathrm{dB}7.9(2)dB for magnetic signal detection and 8.8(3) dB8.8(3)\,\mathrm{dB}8.8(3)dB for magnetic noise sensing, fully accounting for experimental overheads. Finally, we combine these methods to demonstrate a momentum-space-resolved sensing modality that enables detection of spatially correlated magnetic noise at continuously tunable length scales down to 50 nanometers. These observations open the door toward practical applications of interaction-enhanced quantum sensors for nanoscale biological imaging and material characterization.
Solid-state spin defects, particularly the nitrogen-vacancy (NV) center in diamond, have emerged as powerful platforms for exploring quantum many-body physics and quantum metrology. Their exceptional coherence properties and strong dipolar interactions offer unique opportunities to simulate complex quantum dynamics and engineer entangled states for enhanced sensing beyond the standard quantum limit. However, achieving scalable entanglement in these systems is notoriously difficult due to intrinsic disorder and the complex nature of long-range dipole-dipole interactions. This thesis presents both theoretical and experimental advancements in harnessing quantum dynamics in interacting spin ensembles for quantum-enhanced metrology. A central result is the experimental realization of spin squeezing in a dense ensemble of NV centers, demonstrating a clear path toward overcoming classical limits in solid-state platforms. To further formalize and scale these phenomena, this work develops theoretical frameworks for generating robust spin squeezing under realistic experimental conditions. We show that finite-temperature easy-plane magnetism can be actively leveraged to create scalable squeezed states for the dipolar spin systems on regular lattices. Building upon this, we further extend the result to spatially disordered quantum dipoles. We demonstrate that strongly coupled spin pairs suppress squeezing through dynamical heating, and we propose a selective shelving protocol to mitigate this problem. Furthermore, we also propose a universal protocol for quantum-enhanced sensing that exploits information scrambling, utilizing the natural, scrambling dynamics of strongly interacting many-body systems to effectively amplify weak external signals. Together, the findings detailed in this thesis establish a foundational paradigm for controlling and utilizing solid-state spin ensembles, paving the way for entanglement-enhanced quantum sensors.
Solid-state quantum sensors based on ensembles of nitrogen-vacancy (NV) centers in diamond have emerged as powerful platforms for high-precision metrology. Coupling the NV ensemble to a microwave cavity mode in a cavity quantum electrodynamics (cQED) configuration enables spin readout that surpasses the limitations of conventional optical detection, achieving sub-picotesla magnetic sensitivities. However, existing continuous-wave cQED approaches remain far from the intrinsic spin-projection-noise limit due to spin saturation and power broadening. Here, we introduce a dispersive cQED readout technique to overcome these fundamental limitations in NV ensemble sensing. We develop a comprehensive theoretical framework describing the dispersive interaction and analyze the time-domain dynamics of a strongly-coupled NV-cavity system. Our results indicate near-unity inverse readout fidelity and femtotesla-level sensitivity using a commercially available diamond NV ensemble. Importantly, the dispersive readout exhibits a distinct sensitivity scaling that improves as 1/N with increasing number of spins N, providing a practical pathway toward approaching the standard quantum limit for solid-state spin-ensemble sensors.
Controlling the dynamics of targeted quantum correlations is a central goal across many disciplines of quantum science. For applications in nanoscale quantum sensing, nitrogen-vacancy (NV) centers in diamond have recently emerged as a leading platform due to their atom-like nature, exquisite magnetic sensitivity and well-developed coherent control techniques under ambient conditions. However, harnessing the entanglement structure required to improve this sensitivity beyond the standard quantum limit (SQL) from the native dipolar interactions between NV centers is challenging due to their strong positional disorder, three-dimensional geometry and low-fidelity readout. Coupled tightly to proof of principle experimental demonstrations, this thesis provides a theoretical blueprint to realize practical, entanglement-enhanced quantum sensing in the solid-state via far-from-equilibrium dynamics of dense ensembles of NV centers in diamond. Our most fundamental contribution is to identify a universal mechanism exploiting the thermalization of long-wavelength spin textures to generate scalable spin squeezing in the absence of finite temperature symmetry breaking. We further develop a novel sensing protocol based on asymmetric time-reversal capable of rapidly breaking the SQL without high-fidelity readout. Challenging long-standing beliefs in the field, these results open the door to a new era of entanglement-enhanced sensing under ambient conditions, with applications ranging from nanoscale imaging of biological structures to covariance magnetometry of exotic quantum materials.