arXiv subjects

Ilja Fescenko

Publications and source records attributed to Ilja Fescenko.

At least 19 recordsLinked to original sources

arXiv2026

Probing GHz Spin Dynamics Across Magnetic Phase Transitions in CrCl3 Nanoflakes Using Nitrogen-Vacancy Microscopy

CrCl3, a layered van der Waals (vdW) magnet, exhibits in-plane magnetic anisotropy and enhanced interlayer coupling upon stacking, making it an ideal platform to host exotic nanoscale magnetic phenomena such as magnon hydrodynamics and meron-like topological spin defects. When interfaced with other vdW materials, its antiferromagnetic-to-ferromagnetic and ferromagnetic-to-paramagnetic phase transitions and magnetic anisotropy can be tuned by voltage, strain, and layer stacking. Understanding the spin dynamics of CrCl3 at its magnetic phase transitions is crucial to its applications in magnonics. Here, we investigate the spin dynamics of CrCl3 nanoflakes using cryogenic diamond quantum sensing microscopy, based on measuring optically detected magnetic resonance, Rabi oscillations, and spin-lattice relaxation time (T1) of shallow nitrogen vacancy (NV) centers in diamond. In the ferromagnetic regime, we observe a pronounced reduction in the NV spin resonance contrast, a collapse of the Rabi oscillations, and a strong enhancement by two orders of magnitude of the relaxation rate G1 = 1/T1. These observations indicate intensified spin fluctuations in the gigahertz range. Broadband ferromagnetic resonance spectroscopy on CrCl3 crystals reveals resonance frequencies in the 4-15 GHz range together with a linewidth of ~24 mT, further supporting the NV measurements. A phenomenological model of magnetic-noise-induced NV relaxation reproduces the temperature dependence of G1 by combining antiferromagnetic, ferromagnetic, and paramagnetic fluctuation channels, indicating that magnetic noise is strongest in the ferromagnetic regime and evolves markedly across the phase transition. These results are crucial for using CrCl3 in 2D magnonics and hybrid quantum-magnon systems.

cond-mat.mes-hall↗

arXiv2025

Earth's field diamond vector magnetometry with isotropic magnetic flux concentrators

Vector magnetometers based on the optically detected magnetic resonance (ODMR) of nitrogen-vacancy centers in diamond are being developed for applications such as navigation and geomagnetism. However, at low magnetic fields, such as that on Earth (~50 {\mu}T), diamond magnetometers suffer from spectral congestion whereby ODMR peaks are not easily resolved. Here, we experimentally investigate a potential solution of using an isotropic, three-dimensional magnetic flux concentrator to amplify Earth's field without altering its direction. The concentrator consists of six ferrite cones, in a face-centered cubic arrangement, centered about a diamond. We vary the direction of a 50 {\mu}T applied field and record and fit the resulting ODMR spectra. By comparing the fitted fields to those of a reference fluxgate magnetometer, we characterize the angular response of the diamond magnetometer and quantify absolute errors in the field magnitude and angle. We find that the enhancement factor is nearly isotropic, with a mean of 19.05 and a standard deviation of 0.16, when weighted by solid angle coverage. Gradient broadening of the ODMR lines is sufficiently small that the spectra are well resolved for nearly all field directions, alleviating spectral congestion. For ~98% of the total 4{\pi} solid angle, Cram\'er-Rao lower bounds for magnetic field estimation uncertainty are within a factor of 2 of those of the fully-resolved case, indicating minimal deadzones. We track the stability of the magnetometer over six hours and observe variations less than or approximately 40 nT/hour, limited by temperature drift. Our study presents a new route for diamond vector magnetometry at Earth's field, with potential applications in geomagnetic surveys, anomaly detection, and navigation.

physics.ins-det↗

arXiv2025

Nitrogen-Vacancy Magnetometry of Edge Magnetism in WS2 Flakes

Two-dimensional (2D) magnets are of significant interest both as a platform for exploring novel fundamental physics and for their potential in spintronic and optoelectronic devices. Recent bulk magnetometry studies have indicated a weak ferromagnetic response in WS2, and theoretical predictions suggest edge-localized magnetization in flakes with partial hydrogenation. Here, we use room-temperature wide-field quantum diamond magnetometry to image pristine and Fe-implanted WS2 flakes of varying thicknesses (45-160 nm), exfoliated from bulk crystals and transferred to NV-doped diamond substrates. We observe direct evidence of edge-localized stray magnetic fields, which scale linearly with applied external magnetic field (4.4-220 mT), reaching up to 4.7 uT. The edge signal shows a limited dependence on the flake thickness, consistent with dipolar field decay and sensing geometry. Magnetic simulations using five alternative models favor the presence of edge magnetization aligned along an axis slightly tilted from the normal to the WS2 flake plane, consistent with spin canting in antiferromagnetically coupled edge states. Our findings establish WS2 as a promising platform for edge-controlled 2D spintronics.

cond-mat.mes-hall↗

arXiv2025

Quantum diamond microscopy of individual vaterite microspheres containing magnetite nanoparticles

Biocompatible vaterite microspheres, renowned for their porous structure, are promising carriers for magnetic nanoparticles (MNPs) in biomedical applications such as targeted drug delivery and diagnostic imaging. Precise control over the magnetic moment of individual microspheres is crucial for these applications. This study employs widefield quantum diamond microscopy to map the stray magnetic fields of individual vaterite microspheres (3-10 um) loaded with Fe3O4 MNPs of varying sizes (5 nm, 10 nm, and 20 nm). By analyzing over 35 microspheres under a 222 mT external magnetizing field, we measured peak-to-peak stray field amplitudes of 41 uT for 5 nm and 10 nm superparamagnetic MNPs, reflecting their comparable magnetic response, and 12 uT for 20 nm ferrimagnetic MNPs, due to distinct magnetization behavior. Finite-element simulations confirm variations in MNP distribution and magnetization uniformity within the vaterite matrix, with each microsphere encapsulating thousands of MNPs to generate its magnetization. This high-resolution magnetic imaging approach yields critical insights into MNP-loaded vaterite, enabling optimized synthesis and magnetically controlled systems for precision therapies and diagnostics.

physics.bio-ph↗

arXiv2024

The impact of microwave phase noise on diamond quantum sensing

Precision optical measurements of the electron-spin precession of nitrogen-vacancy (NV) centers in diamond form the basis of numerous applications. The most sensitivity-demanding applications, such as femtotesla magnetometry, require the ability to measure changes in GHz spin transition frequencies at the sub-millihertz level, corresponding to a fractional resolution of better than 10^{-12}. Here we study the impact of microwave (MW) phase noise on the response of an NV sensor. Fluctuations of the phase of the MW waveform cause undesired rotations of the NV spin state. These fluctuations are imprinted in the optical readout signal and, left unmitigated, are indistinguishable from magnetic field noise. We show that the phase noise of several common commercial MW generators results in an effective pT s^{1/2}-range noise floor that varies with the MW carrier frequency and the detection frequency of the pulse sequence. The data are described by a frequency domain model incorporating the MW phase noise spectrum and the filter-function response of the sensing protocol. For controlled injection of white and random-walk phase noise, the observed NV magnetic noise floor is described by simple analytic expressions that accurately capture the scaling with pulse sequence length and the number of pi pulses. We outline several strategies to suppress the impact of MW phase noise and implement a version, based on gradiometry, that realizes a >10-fold suppression. Our study highlights an important challenge in the pursuit of sensitive diamond quantum sensors and is applicable to other qubit systems with a large transition frequency.

quant-ph↗

arXiv2024

Imaging Local Effects of Voltage and Boron Doping on Spin Reversal in Antiferromagnetic Magnetoelectric Cr2O3 Thin Films and Devices

Chromia (Cr2O3) is a magnetoelectric oxide which permits voltage-control of the antiferromagnetic (AFM) order, but it suffers technological constraints due to its low Neel Temperature (TN ~307 K) and the need of a symmetry breaking applied magnetic field to achieve reversal of the Neel vector. Recently, boron (B) doping of Cr2O3 films led to an increase TN > 400 K and allowed the realization of voltage magnetic-field free controlled N\'eel vector rotation. Here, we directly image the impact of B doping on the formation of AFM domains in Cr2O3 thin films and elucidate the mechanism of voltage-controlled manipulation of the spin structure using nitrogen vacancy (NV) scanning probe magnetometry. We find a stark reduction and thickness dependence of domain size in B-doped Cr2O3 (B:Cr2O3) films, explained by the increased germ density, likely associated with the B doping. By reconstructing the surface magnetization from the NV stray-field maps, we find a qualitative distinction between the undoped and B-doped Cr2O3 films, manifested by the histogram distribution of the AFM ordering, i.e., 180 degree domains for pure films, and 90 degree domains for B:Cr2O3 films. Additionally, NV imaging of voltage-controlled B-doped Cr2O3 devices corroborate the 90 degeree rotation of the AFM domains observed in magnetotransport measurement.

cond-mat.mtrl-sci↗

arXiv2024

Room Temperature Magnetic Skyrmions in Gradient-Composition Engineered CoPt Single Layers

Topologically protected magnetic skyrmions in magnetic materials are stabilized by interfacial or bulk Dzyaloshinskii-Moriya interaction (DMI). Interfacial DMI decays with increase of the magnetic layer thickness in just a few nanometers and bulk DMI typically stabilizes magnetic skyrmions at low temperatures. Consequently, more flexibility in manipulation of DMI is required for utilizing nanoscale skyrmions in energy efficient memory and logic devices at room temperature (RT). Here, we demonstrate the observation of RT skyrmions stabilized by gradient DMI (g-DMI) in composition gradient engineered CoPt single layer films by employing topological Hall effect, magnetic force microscopy, and nitrogen vacancy scanning magnetometry. Skyrmions remain stable at a wide range of applied magnetic fields and are confirmed to be nearly Bloch-type from micromagnetic simulation and analytical magnetization reconstruction. Furthermore, we observe skyrmion pairs which may be explained by skyrmion-antiskyrmion interactions. Our findings expand the family of magnetic materials hosting RT magnetic skyrmions by tuning g-DMI via gradient polarity and choice of magnetic elements.

cond-mat.mes-hall↗

arXiv2024

Magnetic Relaxometry of Methemoglobin by Widefield Nitrogen-Vacancy Microscopy

Hemoglobin (Hb) is a multifaceted protein, classified as a metalloprotein, chromoprotein, and globulin. It incorporates iron, which plays a crucial role in transporting oxygen within red blood cells. Hb functions by carrying oxygen from the respiratory organs to diverse tissues in the body, where it releases oxygen to fuel aerobic respiration, thus supporting the organism's metabolic processes. Hb can exist in several forms, primarily distinguished by the oxidation state of the iron in the heme group, including Methemoglobin (MetHb). Measuring the concentration of MetHb is crucial because it cannot transport oxygen, hence higher concentration of MetHb in the blood causes methemoglobinemia. Here, we use optically detected magnetic relaxometry of paramagnetic iron spins in MetHb drop-casted onto nanostructured diamond doped with shallow high density nitrogen vacancy (NV) spin qubits. We modify the MetHb concentration in the range of 6 x 10^6 - 1.8 x 10^7 adsorbed Fe+3 spins per um^2 and observe an increase of the NV relaxation rate G1 (= 1/T1, T1 is NV spin lattice relaxation time) up to 2 x 10^3 s^-1. NV magnetic relaxometry of MetHb in phosphate-buffered saline solution shows a similar effect with an increase of G1 to 6.7 x 10e3 s^-1 upon increasing the MetHb concentration to 100 uM. The increase of NV G1 is explained by the increased spin noise coming from the Fe+3 spins present in MetHb proteins. This study presents an additional usage of NV quantum sensors to detect paramagnetic centers of biomolecules at volumes below 100 picoliter.

physics.bio-ph↗

arXiv2023

Nitrogen-Vacancy Magnetic Relaxometry of Nanoclustered Cytochrome C Proteins

Nitrogen-vacancy (NV) magnetometry offers an alternative tool to detect paramagnetic centers in cells with a favorable combination of magnetic sensitivity and spatial resolution. Here, we employ NV magnetic relaxometry to detect cytochrome C (Cyt-C) nanoclusters. Cyt-C is a water-soluble protein that plays a vital role in the electron transport chain of mitochondria. Under ambient conditions, the heme group in Cyt-C remains in the Fe3+ state, which is paramagnetic. We vary the concentration of Cyt-C from 6 to 54 uM and observe a reduction of the NV spin-lattice relaxation time (T1) from 1.2 ms to 150 us, which is attributed to the spin noise originating from the Fe3+ spins. NV T1 imaging of Cyt-C drop-casted on a nanostructured diamond chip allows us to detect the relaxation rates from the adsorbed Fe3+ within Cyt-C.

physics.bio-ph↗

arXiv2023

Ultra-fast detection of the center frequency of a spectral line from amplitude-weighted average

Spectroscopy methods often require calculating the central frequency of a resonance line, that is usually implemented by finding a best fit to the spectrum by a line-shape function. Such an iterative procedure is slow and requires an initial guess. We report an analytical method for calculating the central frequency of a spectral line by using the mean value of its frequencies, which are weighted by corresponding normalized intensities. We use this method to calculate two-dimensional arrays of central frequencies from parallely measured magnetic resonance spectra, which are optically detected by a camera sensor in a thin layer of NV centers with superparamagnetic hemozoin crystals on top of it. We demonstrate that our analytical method is more than 800 times faster than the fitting procedure without significant loss of accuracy. For a 400x400 pixels sensing array, this method is almost instantaneous, while fitting with the Lorentz function requires several minutes of post-processing on a 4-core MacBook Pro. When a resonance is beyond the spectral range, the amplitude-weighted-mean method does not fail, but it alternates its center frequency proportionally to the mismatch distance. Our method will be useful for spectroscopic applications that require high performance of data processing, allowing their fast optimization, inline processing and real-time output of results. It can also be used for automatic analysis of single spectra, when accuracy of the frequency detection could be slightly (<10%) reduced for sake of stability and simplicity of the data processing.

physics.atom-ph↗

arXiv2023

Nitrogen-vacancy magnetometry of individual Fe-triazole spin crossover nanorods

[Fe(Htrz)2(trz)](BF4) (Fe-triazole) spin crossover molecules show thermal, electrical, and optical switching between high spin (HS) and low spin (LS) states, making them promising candidates for molecular spintronics. The LS and HS transitions originate from the electronic configurations of Fe(II), and are considered to be diamagnetic and paramagnetic respectively. The Fe(II) LS state has six paired electrons in the ground states with no interaction with the magnetic field and a diamagnetic behavior is usually observed. While the bulk magnetic properties of Fe-triazole compounds are widely studied by standard magnetometry techniques their properties at the individual level are missing. Here we use nitrogen vacancy (NV) based magnetometry to study the magnetic properties of the Fe-triazole LS state of nanoparticle clusters and individual nanorods of size varying from 20 to 1000 nm. Scanning electron microscopy (SEM) and Raman spectroscopy are performed to determine the size of the nanoparticles/nanorods and to confirm their respective spin state. The magnetic field patterns produced by the nanoparticles/nanorods are imaged by NV magnetic microscopy as a function of applied magnetic field (up to 350 mT) and correlated with SEM and Raman. We found that in most of the nanorods the LS state is slightly paramagnetic, possibly originating from the surface oxidation and/or the greater Fe(III) presence along the nanorod edges. NV measurements on the Fe-triazole LS state nanoparticle clusters revealed both diamagnetic and paramagnetic behavior. Our results highlight the potential of NV quantum sensors to study the magnetic properties of spin crossover molecules and molecular magnets.

cond-mat.mes-hall↗

arXiv2023

Nuclear quadrupole resonance spectroscopy with a femtotesla diamond magnetometer

Sensitive Radio-Frequency (RF) magnetometers that can detect oscillating magnetic fields at the femtotesla level are needed for demanding applications such as Nuclear Quadrupole Resonance (NQR) spectroscopy. RF magnetometers based on Nitrogen-Vacancy (NV) centers in diamond have been predicted to offer femtotesla sensitivity, but published experiments have largely been limited to the picotesla level. Here, we demonstrate a femtotesla RF magnetometer based on an NV-doped diamond membrane inserted between two ferrite flux concentrators. The device operates in bias magnetic fields of 2-10 microtesla and provides a ~300-fold amplitude enhancement within the diamond for RF magnetic fields in the 0.07-3.6 MHz range. The magnetometer's sensitivity is ~70 fT s^{1/2} at 0.35 MHz, and the noise floor decreases to below 2 fT after 1 hour of acquisition. We used this sensor to detect the 3.6 MHz NQR signal of 14N in sodium nitrite powder at room temperature. NQR signals are amplified by a resonant RF coil wrapped around the sample, allowing for higher signal-to-noise ratio detection. The diamond RF magnetometer's recovery time after a strong RF pulse is ~35 us, limited by the coil ring-down time. The sodium-nitrite NQR frequency shifts linearly with temperature as -1.00 +/- 0.02 kHz/K, the magnetization dephasing time is T2* = 887 +/- 51 us, and a spin-lock spin-echo pulse sequence extends the signal lifetime to 332 +/- 23 ms, all consistent with coil-based NQR studies. Our results expand the sensitivity frontier of diamond magnetometers to the femtotesla range, with potential applications in security, medical imaging, and materials science.

physics.ins-det↗

arXiv2022

Nanoscale imaging of antiferromagnetic domains in epitaxial films of Cr2O3 via scanning diamond magnetic probe microscopy

We report direct imaging of boundary magnetization associated with antiferromagnetic domains in magnetoelectric epitaxial Cr2O3 thin films using diamond nitrogen vacancy microscopy. We found a correlation between magnetic domain size and structural grain size which we associate with the domain formation process. We performed field cooling, i.e., cooling from above to below the N\'eel temperature in the presence of magnetic field, which resulted in the selection of one of the two otherwise degenerate 180 degree domains. Lifting of such a degeneracy is achievable with a magnetic field alone due to the Zeeman energy of a weak parasitic magnetic moment in Cr2O3 films that originates from defects and the imbalance of the boundary magnetization of opposing interfaces. This boundary magnetization couples to the antiferromagnetic order parameter enabling selection of its orientation. Nanostructuring the Cr2O3 film with mesa structures revealed reversible edge magnetic states with the direction of magnetic field during field cooling.

cond-mat.mtrl-sci↗

arXiv2021

Tunable magnetic field source for magnetic field imaging microscopy

In this work we present a novel, compact, power efficient magnetic field source design for magnetic field imaging microscopy. The device is based on a pair of diametrically magnetized permanent magnet cylinders with electro-mechanical rotation control and ferrite field concentrators. A Hall probe and NV centers in diamond are used to demonstrate a proof of concept of a proposed magnetic field setup and to characterise the homogeneity of the produced magnetic field on a micrometer scale. Numerical simulation results are compared with experimental results showing good agreement of the distribution of the magnetic field in the setup. As a result, a magnetic field source with a tunable field amplitude in the range from 1 mT to 222 mT is demonstrated, achieving a magnetic field homogeneity of 2 ppm/$\mu$m or 0.5 $\mu$T/$\mu$m at 222 mT in a 25$\times$25 $\mu$m field of view.

physics.app-ph↗

arXiv2021

NV microscopy of thermally controlled stresses caused by Cr$_2$O$_3$ thin films

Many modern applications, including quantum computing and quantum sensing, use substrate-film interfaces. Particularly, thin films of chromium or titanium and their oxides are commonly used to bind various structures, such as resonators, masks, or microwave antennas, to a diamond surface. Due to different thermal expansions of involved materials, such films and structures could produce significant stresses, which need to be measured or predicted. In this paper, we demonstrate imaging of stresses in the top layer of diamond with deposited structures of Cr$_2$O$_3$ at temperatures 19$^{\circ}$C and 37$^{\circ}$C by using stress-sensitive optically detected magnetic resonances (ODMR) in NV centers. We also calculated stresses in the diamond-film interface by using finite-element analysis and correlated them to measured ODMR frequency shifts. As predicted by the simulation, the measured high-contrast frequency-shift patterns are only due to thermal stresses, whose spin-stress coupling constant along the NV axis is 21$\pm$1 MHz/GPa, that is in agreement with constants previously obtained from single NV centers in diamond cantilever. We demonstrate that NV microscopy is a convenient platform for optically detecting and quantifying spatial distributions of stresses in diamond-based photonic devices with micrometer precision and propose thin films as a means for local application of temperature-controlled stresses. Our results also show that thin film structures produce significant stresses in diamond substrates, which should be accounted for in NV-based applications.

physics.app-ph↗

arXiv2019

Diamond magnetometer enhanced by ferrite flux concentrators

Magnetometers based on nitrogen-vacancy (NV) centers in diamond are promising room-temperature, solid-state sensors. However, their reported sensitivity to magnetic fields at low frequencies (<1 kHz) is presently >10 pT s^{1/2}, precluding potential applications in medical imaging, geoscience, and navigation. Here we show that high-permeability magnetic flux concentrators, which collect magnetic flux from a larger area and concentrate it into the diamond sensor, can be used to improve the sensitivity of diamond magnetometers. By inserting an NV-doped diamond membrane between two ferrite cones in a bowtie configuration, we realize a ~250-fold increase of the magnetic field amplitude within the diamond. We demonstrate a sensitivity of ~0.9 pT s^{1/2} to magnetic fields in the frequency range between 10 and 1000 Hz, using a dual-resonance modulation technique to suppress the effect of thermal shifts of the NV spin levels. This is accomplished using 200 mW of laser power and 20 mW of microwave power. This work introduces a new dimension for diamond quantum sensors by using micro-structured magnetic materials to manipulate magnetic fields.

physics.ins-det↗

arXiv2019

Influence of nanostructuring on silicon vacancy center spins in diamond pillars

Color centers in diamond micro and nano structures are under investigation for a plethora of applications. However, obtaining high quality color centers in small structures is challenging, and little is known about how properties such as spin population lifetimes change during the transition from bulk to micro and nano structures. In this manuscript, we studied various ways to prepare diamond samples containing silicon vacancy centers and measured how population lifetimes of orbital states change in pillars as we varied their dimensions from approximately 1 $\mu$m to 120 nm. We also researched the influence of the properties of the diamond substrate and the implantation and annealing methods on the silicon vacancy inhomogeneous linewidth and orbital lifetime. Our measurements show that nominally identical diamond samples can display significantly distinct inhomogeneous broadening. We observed weak indications that restricted vibrational modes in small structures may extend population lifetimes. However, imperfections in the crystal lattice or surface damage caused by etching reduce population lifetimes, especially in the smallest structures.

quant-ph↗

arXiv2019

Two-dimensional nuclear magnetic resonance spectroscopy with a microfluidic diamond quantum sensor

Quantum sensors based on nitrogen-vacancy centers in diamond have emerged as a promising detection modality for nuclear magnetic resonance (NMR) spectroscopy owing to their micron-scale detection volume and non-inductive based detection. A remaining challenge is to realize sufficiently high spectral resolution and concentration sensitivity for multidimensional NMR analysis of picoliter sample volumes. Here, we address this challenge by spatially separating the polarization and detection phases of the experiment in a microfluidic platform. We realize a spectral resolution of 0.65 +/- 0.05 Hz, an order-of-magnitude improvement over previous diamond NMR studies. We use the platform to perform two-dimensional correlation spectroscopy of liquid analytes within an effective ~20 picoliter detection volume. The use of diamond quantum sensors as in-line microfluidic NMR detectors is a significant step towards applications in mass-limited chemical analysis and single cell biology.

physics.ins-det↗