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Physical Review A

Optically detected magnetic resonance in negatively charged nitrogen-vacancy centers in diamond under resonant optical excitation at cryogenic temperatures

Ахмеджанов Ринат Абдулхаевич, Л. А. Гущин, Н. А. Низов, В. А. Низов, D. A. Sobgayda, I. V. Zelensky, Philip Hemmer

Published Dec 28, 2016• 3 citations
Publisher

Abstract

We study optically detected magnetic resonance (ODMR) in diamond ${\mathrm{NV}}^{\ensuremath{-}}$ centers at cryogenic temperatures. We find that when we use resonant optical excitation at zero phonon line wavelength, turning on microwave radiation leads to an increase in fluorescence. This is different from the conventional case of nonresonant optical pumping where microwave radiation instead leads to a decrease in fluorescence. In addition, we observe a significant increase in contrast compared to the nonresonant ODMR. To explain this effect, we propose a theoretical model based on the interaction of the resonant optical radiation with different groups from the inhomogeneously broadened ensemble of ${\mathrm{NV}}^{\ensuremath{-}}$ centers. We find that the effect is temperature dependant and can only be observed at temperatures below 35 K.

DOI
10.1103/physreva.94.063859

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We study optically detected magnetic resonance (ODMR) in diamond NV\ensuremath−{\mathrm{NV}}^{\ensuremath{-}}NV\ensuremath− centers at cryogenic temperatures. We find that when we use resonant optical excitation at zero phonon line wavelength, turning on microwave radiation leads to an increase in fluorescence. This is different from the conventional case of nonresonant optical pumping where microwave radiation instead leads to a decrease in fluorescence. In addition, we observe a significant increase in contrast compared to the nonresonant ODMR. To explain this effect, we propose a theoretical model based on the interaction of the resonant optical radiation with different groups from the inhomogeneously broadened ensemble of NV\ensuremath−{\mathrm{NV}}^{\ensuremath{-}}NV\ensuremath− centers. We find that the effect is temperature dependant and can only be observed at temperatures below 35 K.
We study the spectroscopy of an ensemble of negatively charged nitrogen-vacancy centers in diamond at high temperatures between room temperature and 700K under high vacuum conditions. Spin resonances are studied using optical detection of magnetic resonance (ODMR), and optical spectroscopy is employed to study radiative transitions. Upon increasing the temperature, the intensity of radiative decay in visible and infrared decreased. In addition, the ODMR resonance frequencies were decreased, and the phonon line emission shifted to higher wavelengths. Density functional theory calculation of the zero-field splitting parameter (D) revealed that thermal expansion is not enough to explain the shift in the ODMR frequencies. Fitting the measured intensity of photo-luminescence with the theoretical predictions of the Mott–Seitz model yields the value of 0.22eV for the energy barrier associated with nonradiative decay.
As promising quantum sensors, nitrogen-vacancy (N-VVV) centers in diamond have been widely used in frontier studies in condensed-matter physics, material science, and life sciences. In practical applications, weak laser excitation is favorable as it reduces the side effects of laser irradiation, such as phototoxicity and heating. Here we report a combined theoretical and experimental study of (near) zero-field optically detected magnetic resonance (ODMR) of N-VVV-center ensembles under weak 532-nm laser excitation. In this region, both the width and splitting of the ODMR spectra decrease with increasing laser power. This power dependence is reproduced with a model that accounts for the laser-induced charge neutralization of $\mathrm{N}\text{\ensuremath{-}}{V}^{\ensuremath{-}}$--N+{\mathrm{N}}^{+}N+ pairs, which alters the local electric field environment. These results are useful for the understanding and development of N-VVV-based quantum sensing in light-sensitive applications.
We report a study of the 3E excited-state structure of single negatively charged nitrogen-vacancy (NV) defects in diamond, combining resonant excitation at cryogenic temperatures and optically detected magnetic resonance. A theoretical model is developed and shows excellent agreement with experimental observations. In addition, we show that the two orbital branches associated with the 3E excited state are averaged when operating at room temperature. This study leads to an improved physical understanding of the NV defect electronic structure, which is invaluable for the development of diamond-based quantum information processing.
We study the contrast for electrical and optical readout of NV centers in diamond in dependence of the optical excitation wavelength using different excitation schemes. While the optically detected magnetic resonance (ODMR) works efficiently between 480 and 580 nm, electrically detected magnetic resonance (EDMR) shows a strong dependence on the excitation dynamics. The highest, electrically detected contrast of -23% is achieved by resonantly exciting the zero-phonon line of the neutral charge state of NV at 575 nm. EDMR is also enhanced at 521 nm, possibly due to a further excited state of NV−^-−.
We study cross-relaxation resonances between differently oriented groups of nitrogen-vacancy (NV) centers at small external magnetic fields. These resonances are observed using resonant optical pumping on the NV-center zero phonon line. We suggest a magnetometry protocol that is based on measuring the positions of cross-relaxation resonances on the fluorescence scan. This protocol does not require microwave radiation and can be used to find all components of the unknown magnetic field vector. A room-temperature variant of the protocol with off-resonant optical pumping is also briefly discussed.
We demonstrate the use of two-photon excitation for observing the ground state optically detected magnetic resonance (ODMR) of nitrogen-vacancy centers in diamonds at room temperature. An ultrafast femtosecond laser at 1040 nm was used for excitation, while fluorescence signal read out was achieved through a combination of a PMT and a lock-in amplifier. The imaging capability of two-photon excitation fluorescence (2PEF) was utilized to map the distribution of NV centers in a bulk diamond and micro-sized diamonds. For the first time, ODMR traces of the nitrogen-vacancy center are observed with two-photon excitation, providing a promising tool for fast 3D quantum sensing and imaging.