arXiv subjects

Andrej Denisenko

Publications and source records attributed to Andrej Denisenko.

At least 19 recordsLinked to original sources

arXiv2026

Revealing and reducing growth-induced interfacial disorder in preferentially aligned nitrogen-vacancy centers in diamond

Nitrogen-vacancy (NV) centers in chemical-vapor-deposition (CVD) diamond can form preferentially oriented ensembles with high sensing performance and low densities of lattice defects. Thin films of this material are a cornerstone of various imaging modalities. However, nitrogen injection needed to produce such films can transiently drive growth out of equilibrium, generating interfacial strain and spin defects that degrade NV coherence. Here, we investigate this disorder in $^{12}\text{C}$-enriched, preferentially oriented NV layers grown on (111) diamond using two nitrogen-injection procedures, combined with nanometer-scale selective plasma etching and NV spin-coherence measurements. Pulsed nitrogen injection produces a pronounced nitrogen overshoot within a 60--80 nm interfacial region, generating excessive amounts of defects. By contrast, smooth nitrogen delivery through mass flow controllers substantially suppresses interfacial disorder, yielding coherence properties close to the theoretical limit imposed by spin-bath noise. A 50-nm NV layer is used to demonstrate proton nuclear magnetic resonance detection. This work reveals the role of interfacial disorder associated with the nitrogen-doping procedure and provides a route to growing high-quality, thin NV-doped layers for quantum-sensing applications.

quant-ph↗

arXiv2026

Ramsey correlation spectroscopy with phase cycling using a single quantum sensor

Magnetic spectroscopy at the nanoscale provides unique insights into material properties and dynamics, with quantum sensors like nitrogen-vacancy (NV) centers being ideally suited for these scales. However, detecting low-frequency signals remains a challenge due to finite coherence times ($T_2^*$), as signals oscillating slower than $1/T_2^*$ decay before sufficient phase accumulation occurs. We present RESOLUTE (Ramsey corrElation SpectroscOpy puLse seqUence wiTh phasE cycling), a protocol that overcomes these limitations by combining Ramsey measurements with correlation spectroscopy. By storing accumulated phase as a population imbalance during a correlation period ($T_\mathrm{corr} < T_1$) between two sensing periods, RESOLUTE generates an effective coherence time $T_2^p > T_2^*$. This shifts the frequency-matching condition to the correlation time, enabling detection in the previously inaccessible spectral region between $1/T_1$ and $1/T_2^p$. We experimentally demonstrate an extension of the effective coherence time from $T_2^* = 0.38\,μs$ to $T_2^p = 5.1\,μs$, surpassing Hahn Echo measurements. The technique successfully detects $^{13}$C nuclear spin Larmor precession at fields as low as 49$\,$G ($\sim$50$\,$kHz). We further provide theoretical insight using Fisher information to characterize RESOLUTE's frequency estimation capabilities compared to existing protocols. Finally, by integrating adiabatic pulses and phase cycling, we demonstrate robust spin control and effective DC signal extraction. These advancements provide enhanced sensitivity to weak dipolar interactions, essential for single-molecule imaging and quantum sensing applications.

quant-ph↗

arXiv2026

Sensing single molecule magnets with nitrogen vacancy centers

Single-molecule magnets (SMMs) are molecules that can function as nanoscale magnets with potential use as magnetic memory bits. While SMMs can retain magnetization at low temperatures, characterizing them on surface and at room temperature remains challenging and requires specialized nanoscale techniques. Here, we use single nitrogen-vacancy (NV) centers in diamond as highly sensitive, broadband magnetic field sensors to detect the magnetic noise of cobalt-based SMMs deposited on a diamond surface. We measure the NV relaxation and decoherence times at 296 K and at 5-8 K, observing a significant influence of the SMMs on them. From this, we can infer the SMMs' magnetic noise spectral density (NSD) and underlying magnetic properties. Moreover, we observe the effect of an applied magnetic field on the SMMs' NSD at low temperatures. The method provides nanoscale sensitivity for characterizing SMMs under realistic conditions relevant to their use as surface-bound memory units.

quant-ph↗

arXiv2025

Witnessing non-stationary and non-Markovian environments with a quantum sensor

Quantum sensors offer exceptional sensitivity to nanoscale magnetic fluctuations, where non-stationary effects -- such as spin diffusion -- and non-Markovian dynamics arising from coupling to few environmental degrees of freedom play critical roles. Because fully reconstructing the microscopic structure of realistic spin baths is often infeasible, a practical challenge is to identify the dynamical features that are actually encoded in the sensor's decoherence signal. Here, we demonstrate how quantum sensors can operationally characterize the statistical nature of environmental noise, distinguishing between stationary and non-stationary behaviors, as well as Markovian and non-Markovian dynamics. Using nitrogen-vacancy (NV) centers in diamond as a platform, we develop a physical noise model that captures the essential dynamical features of realistic environments relevant to sensor observables -- independently of the microscopic bath details -- and provides analytical predictions for Ramsey decay across different regimes. These predictions are experimentally validated through controlled noise injection with tunable correlation properties. Our results showcase the capability of quantum sensors to isolate and identify key dynamical properties of complex environments, without requiring full microscopic bath reconstruction. This work clarifies the operational signatures of non-stationarity and non-Markovian behavior at the nanoscale and lays the foundation for strategies that mitigates decoherence while exploiting environmental dynamics for enhanced quantum sensing.

quant-ph↗

arXiv2025

Readout of a solid state spin ensemble at the projection noise limit

Spin ensembles are central to quantum science, from frequency standards and fundamental physics searches to magnetic resonance spectroscopy and quantum sensing. Their performance is ultimately constrained by spin projection noise, yet solid-state implementations have so far been limited by much 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 $^{14}$N nuclear spin bath at high magnetic fields and employing 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.

quant-ph↗

arXiv2025

Deformation-Driven Enhancement of Spin Defect Emission in Hexagonal Boron Nitride

The negatively charged boron vacancy (VB-) in hexagonal boron nitride (hBN) has been extensively investigated as it offers a novel playground for two-dimensional quantum sensing, with ultimate proximity to target samples. However, its practical sensitivity is limited by the intrinsically weak photoluminescence of the spin ensemble. Here, we report a photoluminescence enhancement of up to 30 times from VB- centers in suspended regions of hBN compared to those in substrate-supported areas. The key spin properties, such as the optically detected magnetic resonance (ODMR) contrast and linewidth, as well as the spin lifetime, of the VB- centers in this region are well preserved. Detailed investigations, including measurements of zero-field ODMR, Raman spectroscopy, and Kelvin probe force microscopy, reveal a correlation between emission enhancement and local deformation in the sample. It is concluded that the suspended regions exhibit higher local deformation compared to the supported areas, breaking the local symmetry and thereby activating otherwise forbidden or weak optical transitions of the VB- centers.

quant-ph↗

arXiv2025

Two-Photon Interference of Photons from Remote Tin-Vacancy Centers in Diamond

Scalable quantum networks rely on optical connections between long-lived qubits to distribute entanglement. Tin vacancies in diamond have emerged as promising long-lived qubits, offering extended spin coherence times at liquid helium temperatures and spin-dependent, highly coherent optical transitions for effective photon-based communication. Connecting remote nodes requires quantum interference of indistinguishable photons, which is challenging in an inhomogeneous solid-state environment. Here, we demonstrate a two-node experiment with tin vacancies in diamond, which exhibit a resonant frequency distribution spanning approximately 8 GHz. To overcome the frequency mismatch, we tune the resonant frequencies of one node using the Stark effect. We achieve tunability up to 4 GHz while maintaining optical coherence. As a demonstration, we achieve detuning-dependent remote two-photon interference between separate nodes, obtaining 80(6)% interference visibility without postprocessing when the defects' optical transitions are tuned into resonance, and 63(8)% with detuning up to 20 times their natural linewidths. These results highlight the potential of tin-vacancy centres in diamond for establishing robust optical links between remote quantum registers.

quant-ph↗

arXiv2025

Pulsed magnetic field gradient on a tip for nanoscale imaging of spins

Nanoscale magnetic resonance imaging (nanoMRI) aims at obtaining structure at the single molecule level. Most of the techniques for effecting a nanoMRI gradient use small permanent magnets. Here, we present a switchable magnetic field gradient on a tip, which is designed to provide a local and controllable magnetic field with a high gradient on the nanometer scale. We incorporate the gradient field with a nanoscale magnetic resonance sensor, a single nitrogen-vacancy (NV) center in diamond, to provide high-resolution magnetic resonance imaging. The device is a metal microwire deposited along a quartz tip, with the current flowing along the tip inducing a magnetic field around its apex. This field can be manipulated throughout a measurement by controlling the current along the wire. We achieved gradients as high as 1 $\mathrmμ\text{T/nm}$ at fields weaker than 200 $\mathrmμ\text{T}$. Such a gradient can facilitate electron spin mapping with 1 nm resolution using single NV sensors, allowing for nanoscale imaging of electrons. The ability to switch the current on and off and to position the device with high precision overcomes limitations such as limited emitter contrast and the flexibility in sample preparation. Moreover, we show that proximity of the metallic tip to the sensor modifies the Rabi power in a spatially dependent manner, providing regions with enhanced ($\times$3.5) and decreased Rabi power. This spatial gradient, induced by the tip, offers the opportunity for selective pulses on nearby spin species where the same microwave power will result in different spin manipulation characteristics.

cond-mat.mes-hall↗

arXiv2025

Blueprint for Diamond Magnetometry: Unraveling Quantum Dephasing of Nitrogen-Vacancy Center Ensembles in Diamond

Diamonds with nitrogen-vacancy (NV) center ensembles are one of the most promising solid-state quantum platforms for various sensing applications. The combination of a long spin dephasing time ($T_2^*$) and a high NV center concentration is crucial for pushing the sensitivity limits. In this work, we propose a systematic measurement approach to quantify the electron spin dephasing in NV center ensembles and analyze the contributions of various sources to the dephasing time, including NV-NV interactions, strain and electric field distributions, $^{13}$C nuclear spins, and P1 electron spins. Our method is validated using a series of high-performance diamond samples, providing a comprehensive understanding of dephasing mechanisms and revealing correlations between NV concentration and different dephasing sources. Based on these insights, we further evaluate and propose strategies to improve the achievable sensitivity limits for DC magnetic field measurements.

quant-ph↗

arXiv2024

Discovery of ST2 centers in natural and CVD diamond

The ST2 center is an optically addressable point defect in diamond that facilitates spin initialization and readout. However, while this study presents the discovery of ST2 centers first observed in a natural diamond and provides a reliable technique for artificially creating them, its chemical structure remains unknown. To assess the potential of ST2, we map out its basic optical characteristics, reveal its electronic level structure, and quantify the intrinsic transition rates. Furthermore, we investigate its response to microwaves, static magnetic fields, and the polarization of excitation laser light, revealing twelve inequivalent orientations of the ST2 center. Simultaneous exposure to microwaves and static magnetic fields also reveals an exceptionally wide acceptance angle for sensing strong magnetic fields, unlike the well-established NV center, which is sensitive only within a narrow cone aligned with its symmetry axis. This finding establishes the ST2 center as a highly promising candidate for nanoscale quantum sensing.

physics.optics↗

arXiv2024

Observation of liquid-solid transition of nanoconfined water at ambient temperature

Nanoconfined water plays an indispensable role in various phenomena in biology, chemistry, and engineering. It exhibits many abnormal properties compared to bulk water, especially under strong confinement. However, the origin of those anomalies is still elusive due to the lack of structural information on hydrogen-bonding networks. Considering the inhomogeneity of the nanocavity and the tiny amount of water molecules, conventional optical spectroscopies and nuclear magnetic resonance (NMR) fail to realize the structure analysis of nanoconfined water. Here, we addressed this issue by combining scanning probe microscopy (SPM) with advanced quantum sensing(QS) based on an atomic-size quantum sensor like nitrogen-vacancy (NV) center in diamond, which can apply the nanoscale-NMR for characterizing both the dynamics and structure of confined water at ambient conditions. We built a two-dimensional (2D) nanoconfined water system with a hexagonal-boron nitride (hBN) flake and a hydrophilic diamond surface. By using the SPM tip to measure the confinement size precisely, we observed a critical confinement size of ~2 nm, below which the water diffusion was significantly suppressed and the hydrogen-bonding network of water showed an ordered structure. Meanwhile, molecular dynamics (MD) simulation revealed a solid-like water contact layer on the diamond surface under strong confinement, which also reproduced the measured nanoscale-NMR spectra and confirmed the liquid-solid phase transition observed in the experiments. Notably, with this new SPM-QS platform, our results showed a promising way to elucidate the abnormal properties of nanoconfined water in future applications.

cond-mat.mes-hall↗

arXiv2024

Studying Critical Parameters of Superconductor via Diamond Quantum Sensors

Critical parameters are the key to superconductivity research, and reliable instrumentations can facilitate the study. Traditionally, one has to use several different measurement techniques to measure critical parameters separately. In this work, we develop the use of a single species of quantum sensor to determine and estimate several critical parameters with the help of independent simulation data. We utilize the nitrogen-vacancy (NV) center in the diamond, which recently emerged as a promising candidate for probing exotic features in condensed matter physics. The non-invasive and highly stable nature provides extraordinary opportunities to solve scientific problems in various systems. Using a high-quality single-crystalline YBa$_{2}$Cu$_{4}$O$_{8}$ (YBCO) as a platform, we demonstrate the use of diamond particles and a bulk diamond to probe the Meissner effect. The evolution of the vector magnetic field, the $H-T$ phase diagram, and the map of fluorescence contour are studied via NV sensing. Our results reveal different critical parameters, including lower critical field $H_{c1}$, upper critical field $H_{c2}$, and critical current density $j_{c}$, as well as verifying the unconventional nature of this high-temperature superconductor YBCO. Therefore, NV-based quantum sensing techniques have huge potential in condensed matter research.

cond-mat.mes-hall↗

arXiv2024

Three-dimensional imaging of integrated-circuit activity using quantum defects in diamond

The continuous scaling of semiconductor-based technologies to micron and sub-micron regimes has resulted in higher device density and lower power dissipation. Many physical phenomena such as self-heating or current leakage become significant at such scales, and mapping current densities to reveal these features is decisive for the development of modern electronics. However, advanced non-invasive technologies either offer low sensitivity or poor spatial resolution and are limited to two-dimensional spatial mapping. Here we use near-surface nitrogen-vacancy centres in diamond to probe Oersted fields created by current flowing within a multi-layered integrated circuit in pre-development. We show the reconstruction of the three-dimensional components of the current density with a magnitude down to about $\approx 10 \,\rm μA / μm^2$ and sub-micron spatial resolution at room temperature. We also report the localisation of currents in different layers and observe anomalous current flow in an electronic chip. Our method provides, therefore a decisive step toward three-dimensional current mapping in technologically relevant nanoscale electronics chips.

physics.app-ph↗

arXiv2023

Room temperature relaxometry of single nitrogen-vacancy centers in proximity to $α$-RuCl$_3$ nanoflakes

Investigating spin and charge noise in strongly correlated electron systems is a valuable way to analyze their physical properties and unlock new phases of matter. In this context, nitrogen-vacancy (NV) center-based magnetometry has been proven to be a versatile sensor for various classes of magnetic materials in broad temperature and frequency ranges. Here, we use longitudinal relaxation time $T_1$ of single NV centers to investigate the spin dynamics of nanometers-thin flakes of $α$-RuCl$_3$ at room temperature. We observe a significant reduction in the $T_1$ in the presence of $α$-RuCl$_3$ in proximity to our NVs, which we attribute to paramagnetic spin noise confined in the 2D hexagonal plane. Furthermore, the $T_1$ time exhibits an almost linear increase with an applied external magnetic field. We associate this trend with the alteration of spin and charge noise in $α$-RuCl$_3$ under an external magnetic field. These findings suggest that the influence of the room-temperature spin dynamics of $α$-RuCl$_3$ on the longitudinal relaxation time of the NV center can be used to gain information on the material itself and the technique to be used on other 2D materials.

cond-mat.mes-hall↗

arXiv2023

Quantum-Enhanced Diamond Molecular Tension Microscopy for Quantifying Cellular Forces

The constant interplay and information exchange between cells and their micro-environment are essential to their survival and ability to execute biological functions. To date, a few leading technologies such as traction force microscopy, have been broadly used in measuring cellular forces. However, the considerable limitations, regarding the sensitivity and ambiguities in data interpretation, are hindering our thorough understanding of mechanobiology. Herein, we propose an innovative approach, namely quantum-enhanced diamond molecular tension microscopy (QDMTM), to precisely quantify the integrin-based cell adhesive forces. Specifically, we construct a force sensing platform by conjugating the magnetic nanotags labeled, force-responsive polymer to the surface of diamond membrane containing nitrogen vacancy (NV) centers. Thus, the coupled mechanical information can be quantified through optical readout of spin relaxation of NV centers modulated by those magnetic nanotags. To validate QDMTM, we have carefully performed corresponding measurements both in control and real cell samples. Particularly, we have obtained the quantitative cellular adhesion force mapping by correlating the measurement with established theoretical model. We anticipate that our method can be routinely used in studying important issues like cell-cell or cell-material interactions and mechanotransduction.

q-bio.CB↗

arXiv2023

Dopant-assisted stabilization of negatively charged single nitrogen-vacancy centers in phosphorus-doped diamond at low temperatures

Charge state instabilities have been a bottleneck for the implementation of solid-state spin systems and pose a major challenge to the development of spin-based quantum technologies. Here we investigate the stabilization of negatively charged nitrogen-vacancy (NV$^-$) centers in phosphorus-doped diamond at liquid helium temperatures. Photoionization of phosphorous donors in conjunction with charge diffusion at the nanoscale enhances NV$^0$ to NV$^-$ conversion and stabilizes the NV$^-$ charge state without the need for an additional repump laser. The phosphorus-assisted stabilization is explored and confirmed both with experiments and our theoretical model. Stable photoluminescence-excitation spectra are obtained for NV$^-$ centers created during the growth. The fluorescence is continuously recorded under resonant excitation to real-time monitor the charge state and the ionization and recombination rates are extracted from time traces. We find a linear laser power dependence of the recombination rate as opposed to the conventional quadratic dependence, which is attributed to the photo-ionization of phosphorus atoms.

quant-ph↗

arXiv2023

Real-time frequency estimation of a qubit without single-shot-readout

Quantum sensors can potentially achieve the Heisenberg limit of sensitivity over a large dynamic range using quantum algorithms. The adaptive phase estimation algorithm (PEA) is one example that was proven to achieve such high sensitivities with single-shot readout (SSR) sensors. However, using the adaptive PEA on a non-SSR sensor is not trivial due to the low contrast nature of the measurement. The standard approach to account for the averaged nature of the measurement in this PEA algorithm is to use a method based on `majority voting'. Although it is easy to implement, this method is more prone to mistakes due to noise in the measurement. To reduce these mistakes, a binomial distribution technique from a batch selection was recently shown theoretically to be superior, as all ranges of outcomes from an averaged measurement are considered. Here we apply, for the first time, real-time non-adaptive PEA on a non-SSR sensor with the binomial distribution approach. We compare the mean square error of the binomial distribution method to the majority-voting approach using the nitrogen-vacancy center in diamond at ambient conditions as a non-SSR sensor. Our results suggest that the binomial distribution approach achieves better accuracy with the same sensing times. To further shorten the sensing time, we propose an adaptive algorithm that controls the readout phase and, therefore, the measurement basis set. We show by numerical simulation that adding the adaptive protocol can further improve the accuracy in a future real-time experiment.

quant-ph↗

arXiv2023

Spectroscopy Study on NV Sensors in Diamond-based High-pressure Devices

Recently, the negatively charged nitrogen-vacancy (NV) center has emerged as a robust and versatile quantum sensor in pressurized environments. There are two popular ways to implement NV sensing in a diamond anvil cell (DAC), which is a conventional workhorse in the high-pressure community: create implanted NV centers (INVs) at the diamond anvil tip or immerse NV-enriched nano-diamonds (NDs) in the pressure medium. Nonetheless, there are limited studies on comparing the local stress environments experienced by these sensor types as well as their performances as pressure gauges. In this work, by probing the NV energy levels with the optically detected magnetic resonance (ODMR) method, we experimentally reveal a dramatic difference in the partially reconstructed stress tensors of INVs and NDs incorporated in the same DAC. Our measurement results agree with computational simulations, concluding that INVs perceive a more non-hydrostatic environment dominated by a uniaxial stress along the DAC axis. This provides insights on the suitable choice of NV sensors for specific purposes and the stress distribution in a DAC. We further propose some possible methods, such as using NDs and nanopillars, to extend the maximum working pressure of quantum sensing based on ODMR spectroscopy, since the maximum working pressure could be restricted by non-hydrostaticity of the pressure environment. Moreover, we explore more sensing applications of the NV center by studying how pressure modifies different aspects of the NV system. We perform a photoluminescence study using both INVs and NDs to determine the pressure dependence of the zero-phonon line, which helps developing an all-optical pressure sensing protocol with the NV center. We also characterize the spin-lattice relaxation ($T_1$) time of INVs under pressure to lay a foundation for robust pulsed measurements with NV centers in pressurized environments.

cond-mat.mes-hall↗