Single Nitrogen Vacancy Center In Nanodiamond Research Articles

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

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.

Removing Non-Size-Dependent Electron Spin Decoherence of Nanodiamond Quantum Sensors by Aerobic Oxidation

Fluorescent nanodiamonds (NDs) are crystal defect-based light-emitting nanoparticles that can be applied to quantum information science and quantum sensing. Of particular interest are nitrogen vacancy (NV) centers that allow optical access to their coherently controllable electron spin systems, leading to spin-photon quantum devices and nanoscale sensing of various physical parameters. However, the NV spin coherence time (T2) in NDs has been limited to one or two orders of magnitude shorter than those in bulk diamonds owing to the complicated surface effect that decoheres the NV spin systems. Here, we study the relation between the surface properties and T2 of single NV centers in NDs by systematically analyzing the effect of surface oxidation. We apply aerobic and acidic oxidation methods with various heating temperatures and processing times and find that aerobic oxidation most effectively oxidizes the surface and extends T2 by a factor of 1.6 to the original NDs. The ND-size dependence of T2 clearly shows that the surface oxidation removes a constant decoherence contribution irrespective of the ND size and that a new surface derived decoherence source emerges when the ND size reduces below 50 nm. The present results provide quantitative information on the decoherence sources of NV spin systems of NDs and will enable a strategic surface modification for better spin manipulations of NV centers in the context of quantum information science and nanoscale quantum sensing.

Monitoring spin coherence of single nitrogen-vacancy centers in nanodiamonds during pH changes in aqueous buffer solutions.

We report on the sensing stability of quantum nanosensors in aqueous buffer solutions for the two detection schemes of quantum decoherence spectroscopy and nanoscale thermometry. The electron spin properties of single nitrogen-vacancy (NV) centers in 25 nm-sized nanodiamonds have been characterized by observing individual nanodiamonds during a continuous pH change from 4 to 11. We have determined the stability of the NV quantum sensors during the pH change as the fluctuations of ±12% and ±0.2 MHz for the spin coherence time (T2) and the resonance frequency (ω0) of their mean values, which are comparable to the instrument error of the measurement system. We discuss the importance of characterizing the sensing stability during the pH change and how the present observation affects the measurement scheme of nanodiamond-based NV quantum sensing.

Coupling a Single Nitrogen-Vacancy Center in Nanodiamond to Superparamagnetic Nanoparticles

Single nitrogen-vacancy (NV) defect centers in diamond have been exploited as single photon sources and spin qubits due to their room-temperature robust quantum light emission and long electron spin coherence times. They were coupled to a manifold of structures, such as optical cavities, plasmonic waveguides, and even injected into living cells to study fundamental interactions of various nature at the nanoscale. Of particular interest are applications of NVs as quantum sensors for local nanomagnetometry. Here, we employ a nanomanipulation approach to couple a single NV center in a nanodiamond to a single few-nm superparamagnetic iron oxide nanoparticle in a controlled way. After measuring via relaxometry the magnetic particle spin-noise, we take advantage of the crystal strain ms = ± 1 spin level separation to detect the superparamagnetic particle’s effect in presence of a driving AC magnetic field. Our experiments provide detailed insight in the behavior of such particles with respect to high frequency fields. The approach can be extended to the investigation of increasingly complex, but controlled nanomagnetic hybrid particle assemblies. Moreover, our results suggest that superparamagnetic nanoparticles can amplify local magnetic interactions in order to improve the sensitivity of diamond nanosensors for specific measurement scenarios.

Photoluminescence Enhancement Dependent on the Orientations of Single NV Centers in Nanodiamonds on a Gold Film

We studied the orientations of single Nitrogen-Vacancy (NV) color centers in nanodiamonds on a gold film by defocused imaging with a scanning confocal microscopy system and an electron-multiplying charge-coupled device. It was demonstrated that the perpendicular oriented dipole of single NV color center showed shorter fluorescence lifetime and higher fluorescence intensity than any other oriented ones on account of higher coupling efficiency of local electronic field induced by the surface plasmon resonance on the gold film for a vertical transition dipole.

Energy transfer from a single nitrogen-vacancy center in nanodiamond to a graphene monolayer

In this work, we experimentally demonstrate energy transfer from a single negatively charged nitrogen-vacancy (NV) center in nanodiamond to a graphene monolayer. The mode values of lifetime and intensity of the fluorescence from the single NV center in nanodiamond on monolayer graphene are shorter and weaker than that on bare quartz substrate. The energy transfer efficiency is measured about 40%, consistent with our theoretical estimation.