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arXiv:2512.09043 · Physical Review Letters

Dressed-state Hamiltonian engineering in a strongly interacting solid-state spin ensemble

Haoyang Gao, Nathaniel T. Leitao, Siddharth Dandavate, Lillian B. Hughes Wyatt, Piotr Put, Mathew Mammen, Leigh S. Martin, Hongkun Park, Ania C. Bleszynski Jayich, Mikhail D. Lukin

quant-phSubmitted Dec 9, 2025• Announced Dec 11, 2025• 2 citations
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Abstract

In quantum science applications, ranging from many-body physics to quantum metrology, dipolar interactions in spin ensembles are controlled via Floquet engineering. However, this technique typically reduces the interaction strength between spins, and effectively weakens the coupling to a target sensing field, limiting the metrological sensitivity. In this work, we develop and demonstrate a method for direct tuning of the native interaction in an ensemble of nitrogen-vacancy (NV) centers in diamond. Our approach utilizes dressed-state qubit encoding under a magnetic field perpendicular to the crystal lattice orientation. This method leads to a $3.2\times$ enhancement of the dimensionless coherence parameter $JT_2$ compared to state-of-the-art Floquet engineering, and a $2.6\times$ ($8.3~$dB) enhanced sensitivity in AC magnetometry. Utilizing the extended coherence we experimentally probe spin transport at intermediate to late times. Our results provide a powerful Hamiltonian engineering tool for future studies with NV ensembles and other interacting higher-spin ($S>\frac{1}{2}$) systems.

Comments
7 pages, 4 figures

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In quantum science applications, ranging from many-body physics to quantum metrology, dipolar interactions in spin ensembles are controlled via Floquet engineering. However, this technique typically reduces the interaction strength between spins, and effectively weakens the coupling to a target sensing field, limiting the metrological sensitivity. In this work, we develop and demonstrate a method for direct tuning of the native interaction in an ensemble of nitrogen-vacancy (NV) centers in diamond. Our approach utilizes dressed-state qubit encoding under a magnetic field perpendicular to the crystal lattice orientation. This method leads to a 3.2×3.2\times3.2× enhancement of the dimensionless coherence parameter JT2JT_2JT2​ compared to state-of-the-art Floquet engineering, and a 2.6×2.6\times2.6× (8.3 8.3~8.3 dB) enhanced sensitivity in AC magnetometry. Utilizing the extended coherence we experimentally probe spin transport at intermediate to late times. Our results provide a powerful Hamiltonian engineering tool for future studies with NV ensembles and other interacting higher-spin (S>12S>\frac{1}{2}S>21​) systems.
Improved control and manipulation of quantum systems lies at the heart of modern quantum science and technology, with broad applications ranging from quantum metrology to quantum information science and many-body physics. In this thesis, I will introduce a novel framework for robust Hamiltonian engineering in interacting spin systems, which enables the efficient design of Floquet engineering pulse sequences for qubit and qudit systems that out-perform state-of-the-art control methods by orders of magnitude. As applications of this framework, we utilize a high density ensemble of nitrogen vacancy (NV) centers in diamond, and demonstrate significantly improved control over the disordered, interacting many-body spin system. This enabled the first solid state spin ensemble quantum sensor operating beyond the sensitivity limit imposed by interactions between sensing particles, as well as the observation and understanding of novel dynamical many-body phenomena, including discrete time crystalline order and thermalization dynamics in long-range interacting XXZ spin models.
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.
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.
While quantum devices rely on interactions between constituent subsystems and with their environment to operate, native interactions alone often fail to deliver targeted performance. Coherent pulsed control provides the ability to tailor effective interactions, known as Hamiltonian engineering. We propose a Hamiltonian engineering method that maximizes desired interactions while mitigating deleterious ones by conducting a pulse sequence search using constrained optimization. The optimization formulation incorporates pulse sequence length and cardinality penalties consistent with linear or integer programming. We apply the general technique to magnetometry with solid state spin ensembles in which inhomogeneous interactions between sensing spins limit coherence. Defining figures of merit for broadband Ramsey magnetometry, we present novel pulse sequences which outperform known techniques for homonuclear spin decoupling in both spin-1/2 and spin-1 systems. When applied to nitrogen vacancy (NV) centers in diamond, this scheme partially preserves the Zeeman interaction while zeroing dipolar coupling between negatively charged NV − centers. Such a scheme is of interest for NV − magnetometers which have reached the NV − –NV − coupling limit. We discuss experimental implementation in NV ensembles, as well as applicability of the current approach to more general spin bath decoupling and superconducting qubit control.
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 Strong interactions between defect spins in many-body solid-state quantum systems are a crucial resource for exploring non-classical states. However, they face the key challenge of controlling interactions between the defect spins, since they are spatially fixed inside the host lattice. In this work, we present a dressed state approach to control the effective dipolar coupling between solid-state spins and demonstrate this scheme experimentally using two strongly-coupled nitrogen vacancy (NV) centers in diamond. Through Ramsey spectroscopy on the sensor spin, we detect the change of the effective dipolar field generated by the control spin prepared in different dressed states. To observe the change of interaction dynamics, we deploy spin-lock-based polarization transfer measurements between the two NV spins in different dressed states. This scheme allows us to control the distribution of interaction strengths in strongly interacting spin systems, which can be a valuable tool for generating multi-spin correlated states for quantum-enhanced sensing.