No Arabic abstract
Treatment of lab-grown diamond by electron irradiation and annealing has enabled quantum sensors based on negatively-charged nitrogen-vacancy (NV$^text{-}$) centers to demonstrate record sensitivities. cite{Clevenson2015,Wolf2015,Barry2016,Chatzidrosos2017}. Here we investigate the irradiation and annealing process applied to 28 diamond samples using a new ambient-temperature, all-optical approach. As the presence of the neutrally-charged nitrogen-vacancy (NV$^text{0}$) center is deleterious to sensor performance, this photoluminescence decomposition analysis (PDA) is first employed to determine the concentration ratio of NV$^text{-}$ to NV$^0$ in diamond samples from the measured photoluminescence spectrum. The analysis hinges on (i) isolating each NV charge states emission spectrum and (ii) measuring the NV$^text{-}$ to NV$^0$ emission ratio, which is found to be 2.5$pm$0.5 under low-intensity 532 nm illumination. Using the PDA method, we measure the effects of irradiation and annealing on conversion of substitutional nitrogen to NV centers. Combining these measurements with a phenomenological model for diamond irradiation and annealing, we extract an estimated monovacancy creation rate of $0.52pm 0.26$ cm$^{text{-1}}$ for 1 MeV electron irradiation and an estimated monovacancy diffusion coefficient of 1.8 nm$^2$/s at 850~$^circ$C. Finally we find that irradiation doses $gtrsim 10^{18}$ e$^text{-}$/cm$^2$ deteriorate the NV$^text{-}$ decoherence time $T_2$ whereas $T_1$ is unaffected up to the the maximum investigated dose of $5times 10^{18}$ e$^text{-}$/cm$^2$.
Using pulsed photoionization the coherent spin manipulation and echo formation of ensembles of NV- centers in diamond are detected electrically realizing contrasts of up to 17 %. The underlying spin-dependent ionization dynamics are investigated experimentally and compared to Monte-Carlo simulations. This allows the identification of the conditions optimizing contrast and sensitivity which compare favorably with respect to optical detection.
We investigate the magnetic field dependent photo-physics of individual Nitrogen-Vacancy (NV) color centers in diamond under cryogenic conditions. At distinct magnetic fields, we observe significant reductions in the NV photoluminescence rate, which indicate a marked decrease in the optical readout efficiency of the NVs ground state spin. We assign these dips to excited state level anti-crossings, which occur at magnetic fields that strongly depend on the effective, local strain environment of the NV center. Our results offer new insights into the structure of the NVs excited states and a new tool for their effective characterization. Using this tool, we observe strong indications for strain-dependent variations of the NVs orbital g-factor, obtain new insights into NV charge state dynamics, and draw important conclusions regarding the applicability of NV centers for low-temperature quantum sensing.
We present an enhancement of spin properties of the shallow (<5nm) NV centers by using ALD to deposit titanium oxide layer on the diamond surface. With the oxide layer of an appropriate thickness, increases about 2 up to 3.5 times of both relaxation time and evolution time were achieved and the shallow NV center charge states stabilized as well. Moreover, the coherence time kept almost unchanged. This surface coating technique could produce a protective coating layer of controllable thickness without any damages to the solid quantum system surface, making it possible to prolong T1 time and T2* time, which would be a possible approach to the further packaging technique for the applicating solid quantum devices.
We demonstrate electrical detection of the $^{14}$N nuclear spin coherence of NV centers at room temperature. Nuclear spins are candidates for quantum memories in quantum-information devices and quantum sensors, and hence the electrical detection of nuclear spin coherence is essential to develop and integrate such quantum devices. In the present study, we used a pulsed electrically detected electron-nuclear double resonance technique to measure the Rabi oscillations and coherence time ($T_2$) of $^{14}$N nuclear spins in NV centers at room temperature. We observed $T_2 approx$ 0.9 ms at room temperature. Our results will pave the way for the development of novel electron- and nuclear-spin-based diamond quantum devices.
A single Nitrogen Vacancy (NV) center hosted in a diamond nanocrystal is positioned at the extremity of a SiC nanowire. This novel hybrid system couples the degrees of freedom of two radically different systems, i.e. a nanomechanical oscillator and a single quantum object. The dynamics of the nano-resonator is probed through time resolved nanocrystal fluorescence and photon correlation measurements, conveying the influence of a mechanical degree of freedom given to a non-classical photon emitter. Moreover, by immersing the system in a strong magnetic field gradient, we induce a magnetic coupling between the nanomechanical oscillator and the NV electronic spin, providing nanomotion readout through a single electronic spin. Spin-dependent forces inherent to this coupling scheme are essential in a variety of active cooling and entanglement protocols used in atomic physics, and should now be within the reach of nanomechanical hybrid systems.