arXiv subjects

Simon A. Meynell

Publications and source records attributed to Simon A. Meynell.

15 recordsLinked to original sources

arXiv2026

Engineering and Probing a One-Dimensional Dipolar Spin Ensemble in Diamond

Dimensionality plays a central role in determining the collective behavior of interacting quantum systems. Engineering strongly interacting ensembles of solid-state spin defects in reduced dimensions remains a significant challenge at the interface between the applied and fundamental sciences. Here, we create and characterize a positionally disordered, quasi-one-dimensional spin chain in diamond, consisting of optically dark substitutional nitrogen defects (P1 centers) and optically addressable probe nitrogen-vacancy (NV) centers. Our approach exploits the preferential incorporation of nitrogen along step bunches formed during chemical vapor deposition to achieve both lateral and vertical confinement. Combining spatially resolved materials characterization with nanoscale quantum sensing, we establish the one-dimensional character of the optically dark, unpolarized P1 spin ensemble. We then use correlation spectroscopy to probe local spin autocorrelations and investigate infinite-temperature dipolar spin transport. Our results establish a materials-based route for engineering low-dimensional quantum spin systems.

quant-ph↗

arXiv2026

Harnessing diamond surface features for dense and aligned NV ensembles

Controlling nitrogen doping in diamond is key to advancing nitrogen-vacancy (NV) center devices. We harness the hillock, a typically undesirable surface feature, to incorporate high densities of grown-in, aligned NV-centers on a (001)-oriented substrate. Enhanced cathodoluminescence at hillock sidewalls is correlated via nanoSIMS to up to 1000x greater nitrogen incorporation compared to the planar film. We find that these hillocks are associated with stacking faults and edge-type dislocations, consistent with an origin in surface preparation rather than substrate screw dislocations. Yet, the growth is orderly enough that each of the four hillock sidewalls hosts a distinct NV orientation. A 1.7-2% grown-in NV/substitutional nitrogen (P1) ratio, 4x higher than typical (001)-oriented growth, is measured via NV decoherence analysis. By revealing that spontaneously formed hillocks act as natural laboratories for dense, aligned NV formation, this work motivates systematic investigation of facet-dependent nitrogen incorporation and preferential NV alignment in (001) diamond.

cond-mat.mtrl-sci↗

arXiv2026

Spectral tuning of single T centres by the Stark effect

Among the many solid-state emitters being explored for scalable quantum technologies, the silicon T centre is a leading candidate offering long-lived spin qubits, a telecommunications-band spin-photon interface, and integration with on-chip photonic circuits. However, nanophotonic integration broadens both the inhomogeneous spectral distribution and individual emitter linewidths. Here, we integrate single T centres into silicon nanophotonic cavities with p-i-n diodes for local electronic control. These devices enable Stark tuning up to 30 GHz, sufficient to bring 55(2)% of on-chip T centres into mutual resonance, and demonstrate tunable lifetime reduction across the cavity resonance. A model of the joint excitation probability shows an orders-of-magnitude increase in entanglement rate by tuning distinct emitters into mutual resonance. Luminescence modulation at high reverse biases reveals a transition to a dark charge state. Finally, bias-induced modulation of the optical transition splitting uncovers a potential mechanism for electrically driven excited-state spin mixing via spin-orbit coupling. Localized and individual spectral tuning increases the yield of performant silicon spin-photon interfaces and the number of devices per chip available for large-scale entanglement and quantum information technologies.

quant-ph↗

arXiv2025

Laser-induced spectral diffusion and excited-state mixing of silicon T centres

To find practical application as photon sources for entangled optical resource states or as spin-photon interfaces in entangled networks, semiconductor emitters must produce indistinguishable photons with high efficiency and spectral stability. Nanophotonic cavity integration increases efficiency and bandwidth, but it also introduces environmental charge instability and spectral diffusion. Among various candidates, silicon colour centres have emerged as compelling platforms for integrated-emitter quantum technologies. Here we investigate the dynamics of spectral wandering in nanophotonics-coupled, individual silicon T centres using spectral correlation measurements. We observe that spectral fluctuations are driven predominantly by the near-infrared excitation laser, consistent with a power-dependent Ornstein-Uhlenbeck process, and show that the spectrum is stable for up to 1.5 ms in the dark. We demonstrate a 35x narrowing of the emitter linewidth to 110 MHz using a resonance-check scheme and discuss the advantage for pairwise entanglement rates and optical resource state generators. Finally, we report laser-induced spin-mixing in the excited state and discuss potential mechanisms common to both phenomena. These effects must be considered in calibrating T centre devices for high-performance entanglement generation.

quant-ph↗

arXiv2025

Signal amplification in a solid-state quantum sensor via asymmetric time-reversal of many-body dynamics

Electronic spins of nitrogen vacancy (NV) centers in diamond constitute a promising system for micro- and nano-scale magnetic sensing, due to their operation under ambient conditions, ease of placement in close proximity to sensing targets, and biological compatibility. At high densities, the electronic spins interact through dipolar coupling, which typically limits but can also potentially enhance sensing performance. Here we report the experimental demonstration of many-body signal amplification in a solid-state, room temperature quantum sensor. Our approach utilizes time-reversed two-axis-twisting interactions, engineered through dynamical control of the quantization axis and Floquet engineering in a two-dimensional ensemble of NV centers. Strikingly, we observe that the optimal amplification occurs when the backward evolution time equals twice the forward evolution time, in sharp contrast to the conventional Loschmidt echo. These observations can be understood as resulting from an underlying time-reversed mirror symmetry of the microscopic dynamics, providing key insights into signal amplification and opening the door towards entanglement-enhanced practical quantum sensing.

quant-ph↗

arXiv2025

Spin squeezing in an ensemble of nitrogen-vacancy centers in diamond

Spin squeezed states provide a seminal example of how the structure of quantum mechanical correlations can be controlled to produce metrologically useful entanglement. Such squeezed states have been demonstrated in a wide variety of artificial quantum systems ranging from atoms in optical cavities to trapped ion crystals. By contrast, despite their numerous advantages as practical sensors, spin ensembles in solid-state materials have yet to be controlled with sufficient precision to generate targeted entanglement such as spin squeezing. In this work, we present the first experimental demonstration of spin squeezing in a solid-state spin system. Our experiments are performed on a strongly-interacting ensemble of nitrogen-vacancy (NV) color centers in diamond at room temperature, and squeezing (-0.5 $\pm$ 0.1 dB) is generated by the native magnetic dipole-dipole interaction between NVs. In order to generate and detect squeezing in a solid-state spin system, we overcome a number of key challenges of broad experimental and theoretical interest. First, we develop a novel approach, using interaction-enabled noise spectroscopy, to characterize the quantum projection noise in our system without directly resolving the spin probability distribution. Second, noting that the random positioning of spin defects severely limits the generation of spin squeezing, we implement a pair of strategies aimed at isolating the dynamics of a relatively ordered sub-ensemble of NV centers. Our results open the door to entanglement-enhanced metrology using macroscopic ensembles of optically active spins in solids.

quant-ph↗

arXiv2025

Electrically-triggered spin-photon devices in silicon

Quantum networking and computing technologies demand scalable hardware with high-speed control for large systems of quantum devices. Solid-state platforms have emerged as promising candidates, offering scalable fabrication for a wide range of qubits. Architectures based on spin-photon interfaces allow for highly-connected quantum networks over photonic links, enabling entanglement distribution for quantum networking and distributed quantum computing protocols. With the potential to address these demands, optically-active spin defects in silicon are one proposed platform for building quantum technologies. Here, we electrically excite the silicon T centre in integrated optoelectronic devices that combine nanophotonic waveguides and cavities with p-i-n diodes. We observe single-photon electroluminescence from a cavity-coupled T centre with $g^{(2)}(0)=0.05(2)$. Further, we use the electrically-triggered emission to herald the electron spin state, initializing it with $92(8)\%$ fidelity. This shows, for the first time, electrically-injected single-photon emission from a silicon colour centre and a new method of electrically-triggered spin initialization. These findings present a new telecommunications band light source for silicon and a highly parallel control method for T centre quantum processors, advancing the T centre as a versatile defect for scalable quantum technologies.

quant-ph↗

arXiv2024

A strongly interacting, two-dimensional, dipolar spin ensemble in (111)-oriented diamond

Systems of spins with strong dipolar interactions and controlled dimensionality enable new explorations in quantum sensing and simulation. In this work, we investigate the creation of strong dipolar interactions in a two-dimensional ensemble of nitrogen-vacancy (NV) centers generated via plasma-enhanced chemical vapor deposition (PECVD) on (111)-oriented diamond substrates. We find that diamond growth on the (111) plane yields high incorporation of spins, both nitrogen and NV centers, where the density of the latter is tunable via the miscut of the diamond substrate. Our process allows us to form dense, preferentially aligned, 2D NV ensembles with volume-normalized AC sensitivity down to $η_{AC}$ = 810 pT um$^{3/2}$ Hz$^{-1/2}$. Furthermore, we show that (111) affords maximally positive dipolar interactions amongst a 2D NV ensemble, which is crucial for leveraging dipolar-driven entanglement schemes and exploring new interacting spin physics.

quant-ph↗

arXiv2024

Role of Oxygen in Laser Induced Contamination at Diamond-Vacuum Interfaces

Many modern-day quantum science experiments rely on high-fidelity measurement of fluorescent signals emitted by the quantum system under study. A pernicious issue encountered when such experiments are conducted near a material interface in vacuum is "laser-induced contamination" (LIC): the gradual accretion of fluorescent contaminants on the surface where a laser is focused. Fluorescence from these contaminants can entirely drown out any signal from e.g. optically-probed color centers in the solid-state. Crucially, while LIC appears often in this context, it has not been systematically studied. In this work, we probe the onset and growth rate of LIC for a diamond nitrogen-vacancy center experiment in vacuum, and we correlate the contamination-induced fluorescence intensities to micron-scale physical build-up of contaminant on the diamond surface. Drawing upon similar phenomena previously studied in the space optics community, we use photo-catalyzed oxidation of contaminants as a mitigation strategy. We vary the residual oxygen pressure over 9 orders of magnitude and find that LIC growth is inhibited at near-atmospheric oxygen partial pressures, but the growth rate at lower oxygen pressure is non-monotonic. Finally, we discuss a model for the observed dependence of LIC growth rate on oxygen content and propose methods to extend in situ mitigation of LIC to a wider range of operating pressures.

quant-ph↗

arXiv2023

Long-lived coherences in strongly interacting spin ensembles

Periodic driving has emerged as a powerful tool to control, engineer, and characterize many-body quantum systems. However, the required pulse sequences are often complex, long, or require the ability to control the individual degrees of freedom. In this work, we study how a simple Carr-Purcell Meiboom-Gill (CPMG)-like pulse sequence can be leveraged to enhance the coherence of a large ensemble of spin qubits and serve as an important characterization tool. We implement the periodic drive on an ensemble of dense nitrogen-vacancy (NV) centers in diamond and examine the effect of pulse rotation offset as a control parameter on the dynamics. We use a single diamond sample prepared with several spots of varying NV density, which, in turn, varies the NV-NV dipolar interaction strength. Counter-intuitively, we find that rotation offsets deviating from the ideal π-pulse in the CPMG sequence (often classified as pulse errors) play a critical role in preserving coherence even at nominally zero rotation offset. The cause of the coherence preservation is an emergent effective field that scales linearly with the magnitude of the rotation offset. In addition to extending coherence, we compare the rotation offset dependence of coherence to numerical simulations to measure the disorder and dipolar contributions to the Hamiltonian to quantitatively extract the densities of the constituent spin species within the diamond.

quant-ph↗

arXiv2023

Diamond Surface Functionalization via Visible Light-Driven C-H Activation for Nanoscale Quantum Sensing

Nitrogen-vacancy centers in diamond are a promising platform for nanoscale nuclear magnetic resonance sensing. Despite significant progress towards using NV centers to detect and localize nuclear spins down to the single spin level, NV-based spectroscopy of individual, intact, arbitrary target molecules remains elusive. NV molecular sensing requires that target molecules are immobilized within a few nanometers of NV centers with long spin coherence time. The inert nature of diamond typically requires harsh functionalization techniques such as thermal annealing or plasma processing, limiting the scope of functional groups that can be attached to the surface. Solution-phase chemical methods can be more readily generalized to install diverse functional groups, but they have not been widely explored for single-crystal diamond surfaces. Moreover, realizing shallow NV centers with long spin coherence times requires highly ordered single-crystal surfaces, and solution-phase functionalization has not yet been shown to be compatible with such demanding conditions. In this work, we report a versatile strategy to directly functionalize C-H bonds on single-crystal diamond surfaces under ambient conditions using visible light. This functionalization method is compatible with charge stable NV centers within 10 nm of the surface with spin coherence times comparable to the state of the art. As a proof of principle, we use shallow ensembles of NV centers to detect nuclear spins from functional groups attached to the surface. Our approach to surface functionalization based on visible light-driven C-H bond activation opens the door to deploying NV centers as a broad tool for chemical sensing and single-molecule spectroscopy.

cond-mat.mtrl-sci↗

arXiv2023

Two-dimensional spin systems in PECVD-grown diamond with tunable density and long coherence for enhanced quantum sensing and simulation

Systems of spins engineered with tunable density and reduced dimensionality enable a number of advancements in quantum sensing and simulation. Defects in diamond, such as nitrogen-vacancy (NV) centers and substitutional nitrogen (P1 centers), are particularly promising solid-state platforms to explore. However, the ability to controllably create coherent, two-dimensional spin systems and characterize their properties, such as density, depth confinement, and coherence is an outstanding materials challenge. We present a refined approach to engineer dense ($\gtrsim$1 ppm$\cdot$nm), 2D nitrogen and NV layers in diamond using delta-doping during plasma-enhanced chemical vapor deposition (PECVD) epitaxial growth. We employ both traditional materials techniques, e.g. secondary ion mass spectrometry (SIMS), alongside NV spin decoherence-based measurements to characterize the density and dimensionality of the P1 and NV layers. We find P1 densities of 5-10 ppm$\cdot$nm, NV densities between 1 and 3.5 ppm$\cdot$nm tuned via electron irradiation dosage, and depth confinement of the spin layer down to 1.6 nm. We also observe high (up to 0.74) ratios of P1 to NV centers and reproducibly long NV coherence times, dominated by dipolar interactions with the engineered P1 and NV spin baths.

cond-mat.mtrl-sci↗

arXiv2022

Inducing Skyrmion Flop Transitions in Co$_8$Zn$_8$Mn$_4$ at Room Temperature

Magnetic skyrmions are topologically-protected spin textures that manifest in certain non-centrosymmetric ferromagnets under the right conditions of temperature and field. In thin film skyrmion hosts, demagnetization effects combined with geometric confinement can result in two distinct types of spin textures: those with their axis of symmetry in the plane of the film (IP) and those with their axis pointing out-of-plane (OOP). Here we present Lorentz transmission electron microscopy evidence in conjunction with numerical modeling showing a flop transition between IP and OOP skyrmions in Co$_8$Zn$_8$Mn$_4$ at room temperature. We show that this skyrmion flop transition is controllable via the angle of the external field relative to the film normal and we illustrate how this transition depends on thickness. Finally, we propose a skyrmion-writing device that utilizes the details of this transition.

cond-mat.mtrl-sci↗

arXiv2022

Probing many-body dynamics in a two dimensional dipolar spin ensemble

The most direct approach for characterizing the quantum dynamics of a strongly-interacting system is to measure the time-evolution of its full many-body state. Despite the conceptual simplicity of this approach, it quickly becomes intractable as the system size grows. An alternate framework is to think of the many-body dynamics as generating noise, which can be measured by the decoherence of a probe qubit. Our work centers on the following question: What can the decoherence dynamics of such a probe tell us about the many-body system? In particular, we utilize optically addressable probe spins to experimentally characterize both static and dynamical properties of strongly-interacting magnetic dipoles. Our experimental platform consists of two types of spin defects in diamond: nitrogen-vacancy (NV) color centers (probe spins) and substitutional nitrogen impurities (many-body system). We demonstrate that signatures of the many-body system's dimensionality, dynamics, and disorder are naturally encoded in the functional form of the NV's decoherence profile. Leveraging these insights, we directly characterize the two-dimensional nature of a nitrogen delta-doped diamond sample. In addition, we explore two distinct facets of the many-body dynamics: First, we address a persistent debate about the microscopic nature of spin dynamics in strongly-interacting dipolar systems. Second, we demonstrate direct control over the correlation time of the many-body system. Finally, we demonstrate polarization exchange between NV and P1 centers, opening the door to quantum sensing and simulation using two-dimensional spin-polarized ensembles.

quant-ph↗

arXiv2020

Engineering quantum-coherent defects: the role of substrate miscut in chemical vapor deposition diamond growth

The engineering of defects in diamond, particularly nitrogen-vacancy (NV) centers, is important for many applications in quantum science. A materials science approach based on chemical vapor deposition (CVD) growth of diamond and in-situ nitrogen doping is a promising path toward tuning and optimizing the desired properties of the embedded defects. Herein, with the coherence of the embedded defects in mind, we explore the effects of substrate miscut on the diamond growth rate, nitrogen density, and hillock defect density, and we report an optimal angle range between 0.66° < θ < 1.16° for the purposes of engineering coherent ensembles of NV centers in diamond. We provide a model that quantitatively describes hillock nucleation in the step-flow regime of CVD growth, shedding insight on the physics of hillock formation. We also report significantly enhanced incorporation of nitrogen at hillock defects, opening the possibility for templating hillock-defect-localized NV center ensembles for quantum applications.

physics.app-ph↗