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Quantum Simulation and Nanoscale Sensing of Many-Body Phenomena with Solid-State Spin Defects

G. He

Published Jun 10, 2026• 0 citations
Publisher

Abstract

Emergent phenomena in interacting quantum systems arise from collective behavior that cannot be reduced to single-particle physics. Understanding these phenomena requires platforms capable of both synthesizing many-body states under controlled conditions and probing them at the microscopic scale where correlations originate. Solid-state spin defects, including nitrogen-vacancy (NV) centers in diamond and negatively charged boron vacancy centers in hexagonal boron nitride (hBN), offer precisely this dual capability. In the first part of this dissertation, a strongly interacting NV ensemble is subjected to periodic and quasi-periodic drives to access a long-lived prethermal regime and realize a discrete time quasicrystal (DTQC). In the second part, the boron vacancy center in hBN is developed as a two-dimensional quantum sensor through coherence characterization and isotope engineering, then deployed inside a diamond anvil cell to image stress and magnetism simultaneously at gigapascal pressures, resolving a pressure-induced magnetic phase transition in a Cr$_{1+\delta}$Te$_2$/hBN heterostructure. Moreover, NV scanning cross-relaxometry enables nanoscale mapping of spin defects in hBN, while noise spectroscopy is applied to probe superconducting fluctuations and vortex dynamics in a cuprate thin film. Together, these results demonstrate that solid-state spins provide a versatile experimental framework in which quantum simulation, sensor development, and materials characterization inform and reinforce one another.

DOI
10.7936/rmaz-1251

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Emergent phenomena in interacting quantum systems arise from collective behavior that cannot be reduced to single-particle physics. Understanding these phenomena requires platforms capable of both synthesizing many-body states under controlled conditions and probing them at the microscopic scale where correlations originate. Solid-state spin defects, including nitrogen-vacancy (NV) centers in diamond and negatively charged boron vacancy centers in hexagonal boron nitride (hBN), offer precisely this dual capability. In the first part of this dissertation, a strongly interacting NV ensemble is subjected to periodic and quasi-periodic drives to access a long-lived prethermal regime and realize a discrete time quasicrystal (DTQC). In the second part, the boron vacancy center in hBN is developed as a two-dimensional quantum sensor through coherence characterization and isotope engineering, then deployed inside a diamond anvil cell to image stress and magnetism simultaneously at gigapascal pressures, resolving a pressure-induced magnetic phase transition in a Cr1+δ_{1+\delta}1+δ​Te2_22​/hBN heterostructure. Moreover, NV scanning cross-relaxometry enables nanoscale mapping of spin defects in hBN, while noise spectroscopy is applied to probe superconducting fluctuations and vortex dynamics in a cuprate thin film. Together, these results demonstrate that solid-state spins provide a versatile experimental framework in which quantum simulation, sensor development, and materials characterization inform and reinforce one another.
Abstract Advances in hybrid quantum systems and their precise control are pivotal for developing advanced quantum technologies. Two-dimensional (2D) materials with optically accessible spin defects have emerged as a promising platform for building integrated quantum spin systems due to their exceptional flexibility and scalability. However, experimentally realizing such systems and demonstrating their superiority remains challenging. Here, we present a hybrid spin system operating under ambient conditions, integrating boron vacancy ( VB−{{\rm{V}}}_{{\rm{B}}}^{-}VB−​ V B − ) spins in 2D hexagonal boron nitride flakes with a single nitrogen vacancy (NV) center in 3D single-crystal diamonds. This combined system achieves full controllability and exhibits enhanced performance for nanoscale magnetic sensing, including an improved dynamic range. Moreover, we investigate the rich many-body spin dynamics within the hybrid system, which enables us to estimate the concentration of VB−{{\rm{V}}}_{{\rm{B}}}^{-}VB−​ V B − spins. This work provides a critical foundation for advancing the development of 2D-3D integrated quantum spin systems.
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.
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.
Nitrogen-Vacancy (NV) centers in diamond have been established as exceptionally versatile probes for quantum technologies from sensing to simulation.Owing to the versatility of diamond fabrication, NVs can be integrated into probes with nanoscale resolution and superb sensitivity.\nHowever, because the diamond is host to many other types of defects, the local environment of the NV is unique for each NV, which poses challenges for any devices instrumenting NVs.\nThis thesis contributes to the future of NV technologies along two essential directions.\nFirst, we work towards a more complete understanding of the local charge and strain environments of the NV.\nIn addition to permitting the calibration of these effects for NV probes, we suggest potential uses for the local charges and strain that had previously been considered hindrances.\nSecond, we develop new technologies for NV sensing and simulation.\nOur work integrating NVs into diamond anvil cells opens the door to detecting high pressure phenomena using the NVs as all-in-one sensors.\nFinally, our study of the coherence regimes of the local defect environment of the NV is a step towards versatile quantum simulation in dimensions lower than three.
Optically addressable solid-state spin defects have emerged as powerful multimodal quantum sensors, with nitrogen-vacancy (NV) centers in bulk diamond providing benchmark quantum control and sensitivity under ambient conditions. Embedding such defects in nanodiamonds (NDs) extends these capabilities to mobile probes capable of accessing complex biological and nanoscale environments. Reduced dimensions, however, introduce constraints beyond volumetric spin impurities, notably enhanced lattice strain and surface-induced noise sources, which shorten NV spin relaxation times (T1 and T2) and destabilize the NV charge state, as well as resulting in pronounced particle-to-particle variability in NDs typically produced by top-down approaches. These effects complicate both sensing performance and the quantitative interpretation of multimodal signals in realistic environments. This article provides a structured perspective on the physical mechanisms by which material properties constrain NV behavior in NDs, together with mitigation strategies that shape the robust use of these mobile quantum sensors for biosensing and nanoscale science.
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.