scholarly journals Идентификация NV-центров в синтетических флуоресцентных наноалмазах и контроль дефектности кристаллитов методом электронного парамагнитного резонанса

2022 ◽  
Vol 130 (2) ◽  
pp. 332
Author(s):  
В.Ю. Осипов ◽  
К.В. Богданов ◽  
F. Treussart ◽  
A. Rampersaud ◽  
А.В. Баранов
Keyword(s):  
Surface Defects ◽  
Diamond Particle ◽  
Local Environment ◽  
Nitrogen Vacancy ◽  
Paramagnetic Resonance ◽  
Near Surface ◽  
Nv Center ◽  
Integrated Intensity ◽  
Diamond Powders ◽  
Nv Centers

A 100 nm synthetic diamond particle with a large (> 4 ppm) amount of nitrogen vacancy (NV) centers has been studied. The latter exhibit lines associated with forbidden Delta m_s = 2 and allowed Delta m_s = 1 transitions in the electron paramagnetic resonance (EPR) spectra of the ground state of the NV(-) center. The luminescence intensity of particles in the range 550-800 nm increases with an increase in the irradiation dose of 5 MeV electrons and correlates with the integrated intensity of the EPR line with a g-factor g = 4.27.This value is used to estimate the concentration of NV(-) centers and to select diamond powders with the highest fluorescence intensity. The dependence of the EPR signal intensity of the Delta m_s = 2 transition of the NV(-) center on the microwave power has the form of a curve with saturation and subsequent decay, and rather well characterizes the crystal quality of the local environment of the centers under study in these particles. The intensity of the x,y Delta m_s = 1 transition (at ~281.2 mT, 9.444 GHz) turns out to be more sensitive to changes in particle size in the submicron range and the appearance of near-surface defects obtained during mechanical processing.

scholarly journals Readout and control of an endofullerene electronic spin

2020 ◽  
Vol 11 (1) ◽  
Author(s):  
Dinesh Pinto ◽  
Domenico Paone ◽  
Bastian Kern ◽  
Tim Dierker ◽  
René Wieczorek ◽  
...  
Keyword(s):  
Self Assembly ◽  
Large Scale ◽  
Dipolar Interaction ◽  
Nitrogen Vacancy ◽  
Zero Field ◽  
Zero Field Splitting ◽  
Paramagnetic Resonance ◽  
Near Surface ◽  
Atomic Spins ◽  
And Control

AbstractAtomic spins for quantum technologies need to be individually addressed and positioned with nanoscale precision. C60 fullerene cages offer a robust packaging for atomic spins, while allowing in-situ physical positioning at the nanoscale. However, achieving single-spin level readout and control of endofullerenes has so far remained elusive. In this work, we demonstrate electron paramagnetic resonance on an encapsulated nitrogen spin (14N@C60) within a C60 matrix using a single near-surface nitrogen vacancy (NV) center in diamond at 4.7 K. Exploiting the strong magnetic dipolar interaction between the NV and endofullerene electronic spins, we demonstrate radio-frequency pulse controlled Rabi oscillations and measure spin-echos on an encapsulated spin. Modeling the results using second-order perturbation theory reveals an enhanced hyperfine interaction and zero-field splitting, possibly caused by surface adsorption on diamond. These results demonstrate the first step towards controlling single endofullerenes, and possibly building large-scale endofullerene quantum machines, which can be scaled using standard positioning or self-assembly methods.

scholarly journals Monitoring Dark-State Dynamics of a Single Nitrogen-Vacancy Center in Nanodiamond by Auto-Correlation Spectroscopy: Photonionization and Recharging

Nanomaterials ◽  
2021 ◽  
Vol 11 (4) ◽  
pp. 979
Author(s):  
Mengdi Zhang ◽  
Bai-Yan Li ◽  
Jing Liu
Keyword(s):  
Laser Power ◽  
Time Course ◽  
Correlation Spectroscopy ◽  
Nitrogen Vacancy ◽  
Transition Time ◽  
Dark State ◽  
Auto Correlation ◽  
Nv Center ◽  
Photon Process ◽  
Nv Centers

In this letter, the photon-induced charge conversion dynamics of a single Nitrogen-Vacancy (NV) center in nanodiamond between two charge states, negative (NV−) and neutral (NV0), is studied by the auto-correlation function. It is observed that the ionization of NV− converts to NV0, which is regarded as the dark state of the NV−, leading to fluorescence intermittency in single NV centers. A new method, based on the auto-correlation calculation of the time-course fluorescence intensity from NV centers, was developed to quantify the transition kinetics and yielded the calculation of transition rates from NV− to NV0 (ionization) and from NV0 to NV− (recharging). Based on our experimental investigation, we found that the NV−-NV0 transition is wavelength-dependent, and more frequent transitions were observed when short-wavelength illumination was used. From the analysis of the auto-correlation curve, it is found that the transition time of NV− to NV0 (ionization) is around 0.1 μs, but the transition time of NV0 to NV− (recharging) is around 20 ms. Power-dependent measurements reveal that the ionization rate increases linearly with the laser power, while the recharging rate has a quadratic increase with the laser power. This difference suggests that the ionization in the NV center is a one-photon process, while the recharging of NV0 to NV− is a two-photon process. This work, which offers theoretical and experimental explanations of the emission property of a single NV center, is expected to help the utilization of the NV center for quantum information science, quantum communication, and quantum bioimaging.

NV-Diamond Magnetometer Using Electron Irradiation

2013 ◽  
Vol 1511 ◽  
Author(s):  
Edwin Kim ◽  
Victor M. Acosta ◽  
Erik Bauch ◽  
Dmitry Budker ◽  
Philip R. Hemmer
Keyword(s):  
Electron Spin ◽  
Electron Irradiation ◽  
Spin Transition ◽  
High Sensitivity ◽  
Future Generation ◽  
Nitrogen Vacancy ◽  
Logic Device ◽  
Wide Range ◽  
Nv Center ◽  
Nv Centers

ABSTRACTNitrogen-vacancy (NV) center in diamond is an emerging system for quantum-logic device and sensor applications. The key feature of the NV center is the ability of spin manipulation at room temperature. We apply a wide range of electron irradiation to generate the NV centers in nitrogen-rich diamond for creating best sensitivity. The NV0 and NV─ concentrations in electron irradiated diamond are determined from optical spectra. Additionally, electron spin resonance (ESR) has also proven to be an effective method for probing the electron spin transition between |ms=±1> and |ms=0> states of the NV centers. A study of ESR frequency shift and signal broadening and magnetometer sensitivity as a function of electron irradiation dose has been conducted. The research presented herein is a demonstration of minimum detectable magnetic field tailoring required for future-generation high-sensitivity diamond magnetometry.

scholarly journals Nitrogen-vacancy centers in diamond for nanoscale magnetic resonance imaging applications

2019 ◽  
Vol 10 ◽  
pp. 2128-2151 ◽  
Author(s):  
Alberto Boretti ◽  
Lorenzo Rosa ◽  
Jonathan Blackledge ◽  
Stefania Castelletto
Keyword(s):  
Magnetic Resonance Imaging ◽  
Magnetic Resonance ◽  
High Resolution ◽  
Point Defect ◽  
Nitrogen Vacancy ◽  
Resonance Imaging ◽  
Magnetic Imaging ◽  
Nv Center ◽  
Nitrogen Vacancy Centers ◽  
Nv Centers

The nitrogen-vacancy (NV) center is a point defect in diamond with unique properties for use in ultra-sensitive, high-resolution magnetometry. One of the most interesting and challenging applications is nanoscale magnetic resonance imaging (nano-MRI). While many review papers have covered other NV centers in diamond applications, there is no survey targeting the specific development of nano-MRI devices based on NV centers in diamond. Several different nano-MRI methods based on NV centers have been proposed with the goal of improving the spatial and temporal resolution, but without any coordinated effort. After summarizing the main NV magnetic imaging methods, this review presents a survey of the latest advances in NV center nano-MRI.

Nanoscale Nuclear Magnetic Resonance with a Nitrogen-Vacancy Spin Sensor

Science ◽  
2013 ◽  
Vol 339 (6119) ◽  
pp. 557-560 ◽  
Author(s):  
H. J. Mamin ◽  
M. Kim ◽  
M. H. Sherwood ◽  
C. T. Rettner ◽  
K. Ohno ◽  
...  
Keyword(s):  
Nuclear Magnetic Resonance ◽  
Magnetic Resonance ◽  
Proton Spin ◽  
Nitrogen Vacancy ◽  
Detection Methods ◽  
Near Surface ◽  
Organic Sample ◽  
Nv Center ◽  
Field Fluctuations ◽  
Nuclear Magnetic

Extension of nuclear magnetic resonance (NMR) to nanoscale samples has been a longstanding challenge because of the insensitivity of conventional detection methods. We demonstrated the use of an individual, near-surface nitrogen-vacancy (NV) center in diamond as a sensor to detect proton NMR in an organic sample located external to the diamond. Using a combination of electron spin echoes and proton spin manipulation, we showed that the NV center senses the nanotesla field fluctuations from the protons, enabling both time-domain and spectroscopic NMR measurements on the nanometer scale.

Electron Channelling Contrast Imaging of Dislocations

1990 ◽  
Vol 48 (1) ◽  
pp. 600-601
Author(s):  
J.T. Czernuszka ◽  
N.J. Long ◽  
P.B. Hirsch
Keyword(s):  
Field Emission ◽  
Secondary Electron ◽  
Surface Defects ◽  
Spot Size ◽  
Beam Divergence ◽  
Contrast Imaging ◽  
Scattered Electron ◽  
Near Surface ◽  
Filter System ◽  
Electron Channelling

In the 1970s there was considerable interest in the development of the electron channelling contrast imaging (ECCI) technique for imaging near surface defects in bulk (electron opaque) specimens. The predictions of the theories were realised experimentally by Morin et al., who used a field emission gun (FEG) operating at 40-50kV and an energy filter such that only electrons which had lost no more than a few 100V were detected. This paper presents the results of a set of preliminary experiments which show that an energy filter system is unneccessary to image and characterise the Burgers vectors of dislocations in bulk specimens. The examples in the paper indicatethe general versatility of the technique.A VG HB501 STEM with a FEG was operated at 100kV. A single tilt cartridge was used in the reflection position of the microscope. A retractable back-scattered electron detector was fitted into the secondary electron port and positioned to within a few millimetres of the specimen. The image was acquired using a Synoptics Synergy framestore and digital scan generator and subsequently processed using Semper 6. The beam divergence with the specimen in this position was 2.5 mrads with a spot size of approximately 4nm. Electron channelling patterns were used to orientate the sample.

Direct Plan View FIB Liftout for Near-Surface Defect Analysis in TEM

2013 ◽  
Author(s):  
Max L. Lifson ◽  
Carla M. Chapman ◽  
D. Philip Pokrinchak ◽  
Phyllis J. Campbell ◽  
Greg S. Chrisman ◽  
...  
Keyword(s):  
Failure Analysis ◽  
Silicon Germanium ◽  
Focused Ion Beam ◽  
Surface Defects ◽  
Ion Beam ◽  
Misfit Dislocations ◽  
Tem Analysis ◽  
Plan View ◽  
Near Surface ◽  
Straightforward Method

Abstract Plan view TEM imaging is a powerful technique for failure analysis and semiconductor process characterization. Sample preparation for near-surface defects requires additional care, as the surface of the sample needs to be protected to avoid unintentionally induced damage. This paper demonstrates a straightforward method to create plan view samples in a dual beam focused ion beam (FIB) for TEM studies of near-surface defects, such as misfit dislocations in heteroepitaxial growths. Results show that misfit dislocations are easily imaged in bright-field TEM and STEM for silicon-germanium epitaxial growth. Since FIB tools are ubiquitous in semiconductor failure analysis labs today, the plan view method presented provides a quick to implement, fast, consistent, and straightforward method of generating samples for TEM analysis. While this technique has been optimized for near-surface defects, it can be used with any application requiring plan view TEM analysis.

scholarly journals Sensing Electrochemical Signals Using a Nitrogen-Vacancy Center in Diamond

Nanomaterials ◽  
2021 ◽  
Vol 11 (2) ◽  
pp. 358
Author(s):  
Hossein T. Dinani ◽  
Enrique Muñoz ◽  
Jeronimo R. Maze
Keyword(s):  
Electric Field ◽  
Electron Spin ◽  
Electrolyte Solution ◽  
High Sensitivity ◽  
Theoretical Work ◽  
Coherence Time ◽  
Nitrogen Vacancy ◽  
Local Concentration ◽  
Concentration Of Ions ◽  
Nv Center

Chemical sensors with high sensitivity that can be used under extreme conditions and can be miniaturized are of high interest in science and industry. The nitrogen-vacancy (NV) center in diamond is an ideal candidate as a nanosensor due to the long coherence time of its electron spin and its optical accessibility. In this theoretical work, we propose the use of an NV center to detect electrochemical signals emerging from an electrolyte solution, thus obtaining a concentration sensor. For this purpose, we propose the use of the inhomogeneous dephasing rate of the electron spin of the NV center (1/T2★) as a signal. We show that for a range of mean ionic concentrations in the bulk of the electrolyte solution, the electric field fluctuations produced by the diffusional fluctuations in the local concentration of ions result in dephasing rates that can be inferred from free induction decay measurements. Moreover, we show that for a range of concentrations, the electric field generated at the position of the NV center can be used to estimate the concentration of ions.

scholarly journals High-Quality Green-Emitting Nanodiamonds Fabricated by HPHT Sintering of Polycrystalline Shockwave Diamonds

2020 ◽  
Vol 15 (1) ◽  
Author(s):  
Vladimir Yu. Osipov ◽  
Fedor M. Shakhov ◽  
Kirill V. Bogdanov ◽  
Kazuyuki Takai ◽  
Takuya Hayashi ◽  
...  
Keyword(s):  
Polycrystalline Diamond ◽  
Particle Beam ◽  
Production Method ◽  
High Energy ◽  
Nitrogen Vacancy ◽  
High Energy Particle ◽  
Paramagnetic Resonance ◽  
Precursor Material ◽  
Mean Size ◽  
Characteristic Features

Abstract We demonstrate a high-pressure, high-temperature sintering technique to form nitrogen-vacancy-nitrogen centres in nanodiamonds. Polycrystalline diamond nanoparticle precursors, with mean size of 25 nm, are produced by the shock wave from an explosion. These nanoparticles are sintered in the presence of ethanol, at a pressure of 7 GPa and temperature of 1300 °C, to produce substantially larger (3–4 times) diamond crystallites. The recorded spectral properties demonstrate the improved crystalline quality. The types of defects present are also observed to change; the characteristic spectral features of nitrogen-vacancy and silicon-vacancy centres present for the precursor material disappear. Two new characteristic features appear: (1) paramagnetic substitutional nitrogen (P1 centres with spin ½) with an electron paramagnetic resonance characteristic triplet hyperfine structure due to the I = 1 magnetic moment of the nitrogen nuclear spin and (2) the green spectral photoluminescence signature of the nitrogen-vacancy-nitrogen centres. This production method is a strong alternative to conventional high-energy particle beam irradiation. It can be used to easily produce purely green fluorescing nanodiamonds with advantageous properties for optical biolabelling applications.

Sign in / Sign up

Export Citation Format

Share Document