Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Log inSign up
Challenges
Datasets
Workspaces
Papers
Discussions
Leaderboard
Blog
Job Board
Q3AS

© 2026 Aqora Quantum S.A.S.

TermsPrivacyLegal Notice

arXiv:2308.13351 · Physical Review Applied

Optically detected magnetic resonance of nitrogen-vacancy centers in diamond under weak laser excitation

Yong-Hong Yu, Ruizhi Zhang, Yue Xu, Xiu-Qi Chen, Huijie Zheng, Quan Li, Ren‐Bao Liu, Xinyu Pan, Dmitry Budker, Gang‐Qin Liu

Published Apr 26, 2024• 23 citations
arXivHTMLPDF

Abstract

As promising quantum sensors, nitrogen-vacancy (N-$V$) 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-$V$-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 $\mathrm{N}\text{\ensuremath{-}}{V}^{\ensuremath{-}}$--${\mathrm{N}}^{+}$ pairs, which alters the local electric field environment. These results are useful for the understanding and development of N-$V$-based quantum sensing in light-sensitive applications.

DOI
10.1103/physrevapplied.21.044051

Related papers

Photoconversion of shallow nitrogen-vacancy centers in flat and nanostructured diamond under high-power laser irradiation

Federico Gorrini, C. Dorigoni, Domingo Olivares-Postigo +4 more

Shallow, negatively-charged Nitrogen-Vacancy centers (NV-) in diamond have been proposed for high-sensitivity magnetometry and spin-polarization transfer applications. However, surface effects tend to favor and stabilize the less useful neutral form, the NV0 centers. Here, we report the effects of green laser irradiation on ensembles of nanometer-shallow NV centers in flat and nanostructured diamond surfaces as a function of laser power in a range not previously explored (up to 150 mW/μm2). Raman spectroscopy, optically-detected-magnetic-resonance (ODMR) and charge-photoconversion fluorescence detection are applied to characterize the properties and dynamics of NV- and NV0 centers. We demonstrate that high laser power strongly promotes photoconversion of NV0 to NV- centers. Surprisingly, the excess NV- population is stable over a time scale of one hundred milliseconds after switching off the laser, resulting in long-lived enrichment of shallow NV-. The beneficial effect of photoconversion is less marked in nanostructured samples. Our results are important to inform the design of samples and experimental procedures for applications relying on ensembles of shallow NV- centers in diamond.

arXiv:2105.04939•May 11, 2021•0 citations

Laser-induced thermal effects on ODMR in NV-ensemble diamond at ambient and vacuum

Mohammed Attrash, Tamara Amro, Ilya Simanovsky +5 more

The spin dynamics of the negatively charged nitrogen-vacancy (NV⁻) centers in diamond are highly sensitive to quantum electromagnetic fluctuations arising from optical excitation, chemical interactions, and thermal processes. Here we investigated the optical and spin properties of ensembles of NV⁻ centers in diamond under continuous-wave (CW) and nanosecond pulsed laser excitation. Optical detection of magnetic resonance (ODMR) is employed to monitor laser induced shifts of the zero-field splitting parameter D under ambient and high-vacuum conditions. Increasing CW laser power results in a systematic downshift of the resonance frequency due to laser-induced heating. The effect is significantly enhanced under vacuum, where the shift in D reaches up to ~17 MHz, compared to ~5 MHz in air, emphasizing the role of environmental thermal dissipation. Under nanosecond pulsed excitation, increasing the pulse repetition rate similarly leads to resonance shifts and reduced ODMR contrast, consistent with cumulative thermal effects. Visible and infrared spectroscopy confirm power dependent modifications of NV emission. Time resolved photoluminescence measurements showed that the excited-state lifetime (~6 ns) remains nearly constant across the investigated excitation range, indicating that in this regime the dominant limitation is thermal loading of the spin resonance rather than a change in intrinsic radiative decay dynamics. These results provide a comprehensive characterization of thermal effects in high power optical excitation of NV ensembles and are directly relevant for high intensity NV-based sensing and spectroscopy, particularly in vacuum environments.

Diamond and Related Materials•Mar 26, 2026•0 citations

Optically detected magnetic resonance of nitrogen-vacancy centers in diamond using two-photon excitation

Lam T. Nguyen, Khanh Kieu

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.

quant-pharXiv:2604.15755•Apr 20, 2026•0 citations

Long-Lived Ensembles of Shallow NV– Centers in Flat and Nanostructured Diamonds by Photoconversion

Federico Gorrini, C. Dorigoni, Domingo Olivares-Postigo +4 more

Shallow, negatively charged nitrogen-vacancy centers (NV -) in diamond have been proposed for high-sensitivity magnetometry and spin-polarization transfer applications.However, surface effects tend to favor and stabilize the less useful neutral form, the NV 0 centers.Here, we report the effects of green laser irradiation on ensembles of nanometer-shallow NV centers in flat and nanostructured diamond surfaces as a function of laser power in a range not previously explored (up to 150 mW/μm 2 ).Fluorescence spectroscopy, optically detected magnetic resonance (ODMR), and charge-photoconversion detection are applied to characterize the properties and dynamics of NV -and NV 0 centers.We demonstrate that high laser power strongly promotes photoconversion of NV 0 to NV -centers.Surprisingly, the excess NV -population is stable over a timescale of 100 ms after switching off the laser, resulting in long-lived enrichment of shallow NV -.The beneficial effect of photoconversion is less marked in nanostructured samples.Our results are important to inform the design of samples and experimental procedures for applications relying on ensembles of shallow NV -centers in diamond.

ACS Applied Materials & Interfaces•Sep 1, 2021•21 citations

Characterization of low-nitrogen quantum diamond for pulsed magnetometry applications

Jiashen Tang, Connor Roncaioli, Andrew Mark Edmonds +4 more

Ensembles of nitrogen-vacancy (NV) centers in diamond are versatile quantum sensors with broad applications in the physical and life sciences. The concentration of neutral substitutional nitrogen ( [ N s 0 ]) strongly influences NV electronic spin coherence times, sensitivity, and optimal sensing strategies. Diamonds with [ N s 0 ] ∼ 1–10 ppm are a focus of recent material engineering efforts, with higher concentrations being favorable for continuous-wave optically detected magnetic resonance (CW-ODMR) and lower concentrations expected to benefit pulsed magnetometry techniques through extended NV spin coherence times and improved sensing duty cycles. In this work, we synthesize and characterize low- [ N s 0 ] ( ∼ 0.8 ppm), NV-enriched diamond material, engineered through low-strain chemical vapor deposition (CVD) growth on high-quality substrates, 12 C isotopic purification, and controlled electron irradiation and annealing. Our results demonstrate good strain homogeneity in diamonds grown on CVD substrates and spin-bath-limited NV dephasing times. By measuring NV spin and charge properties across a wide range of optical NV excitation intensity, we provide direct comparisons of photon-shot-noise-limited magnetic field sensitivity between the current low- [ N s 0 ] and previously studied higher- [ N s 0 ] ( ∼ 14 ppm) NV-diamond sensors. We show that low- [ N s 0 ] diamond can outperform higher- [ N s 0 ] diamond at moderate and low optical NV excitation intensity. Our results provide practical benchmarks and guidance for selecting NV-diamond sensors tailored to specific experimental constraints and sensing requirements.

arXiv:2509.06884•Frontiers in Quantum Science and Technology•Dec 9, 2025•0 citations

Optically detected magnetic resonance of nitrogen-vacancy centers in diamond using two-photon excitation

Lam T. Nguyen, Khanh Quoc Kieu

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 readout 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 relative distribution of NV centers in a bulk diamond and micro-sized diamonds. For the first time, to the best of our knowledge, ODMR traces of the nitrogen-vacancy center are observed with two-photon excitation, providing a promising tool for fast 3D quantum sensing and imaging.

Optics Letters•Jun 22, 2026•0 citations
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 N\ensuremath-V\ensuremath−\mathrm{N}\text{\ensuremath{-}}{V}^{\ensuremath{-}}N\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.
Shallow, negatively-charged Nitrogen-Vacancy centers (NV-) in diamond have been proposed for high-sensitivity magnetometry and spin-polarization transfer applications. However, surface effects tend to favor and stabilize the less useful neutral form, the NV0 centers. Here, we report the effects of green laser irradiation on ensembles of nanometer-shallow NV centers in flat and nanostructured diamond surfaces as a function of laser power in a range not previously explored (up to 150 mW/μm2). Raman spectroscopy, optically-detected-magnetic-resonance (ODMR) and charge-photoconversion fluorescence detection are applied to characterize the properties and dynamics of NV- and NV0 centers. We demonstrate that high laser power strongly promotes photoconversion of NV0 to NV- centers. Surprisingly, the excess NV- population is stable over a time scale of one hundred milliseconds after switching off the laser, resulting in long-lived enrichment of shallow NV-. The beneficial effect of photoconversion is less marked in nanostructured samples. Our results are important to inform the design of samples and experimental procedures for applications relying on ensembles of shallow NV- centers in diamond.
The spin dynamics of the negatively charged nitrogen-vacancy (NV⁻) centers in diamond are highly sensitive to quantum electromagnetic fluctuations arising from optical excitation, chemical interactions, and thermal processes. Here we investigated the optical and spin properties of ensembles of NV⁻ centers in diamond under continuous-wave (CW) and nanosecond pulsed laser excitation. Optical detection of magnetic resonance (ODMR) is employed to monitor laser induced shifts of the zero-field splitting parameter D under ambient and high-vacuum conditions. Increasing CW laser power results in a systematic downshift of the resonance frequency due to laser-induced heating. The effect is significantly enhanced under vacuum, where the shift in D reaches up to ~17 MHz, compared to ~5 MHz in air, emphasizing the role of environmental thermal dissipation. Under nanosecond pulsed excitation, increasing the pulse repetition rate similarly leads to resonance shifts and reduced ODMR contrast, consistent with cumulative thermal effects. Visible and infrared spectroscopy confirm power dependent modifications of NV emission. Time resolved photoluminescence measurements showed that the excited-state lifetime (~6 ns) remains nearly constant across the investigated excitation range, indicating that in this regime the dominant limitation is thermal loading of the spin resonance rather than a change in intrinsic radiative decay dynamics. These results provide a comprehensive characterization of thermal effects in high power optical excitation of NV ensembles and are directly relevant for high intensity NV-based sensing and spectroscopy, particularly in vacuum environments.
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.
Shallow, negatively charged nitrogen-vacancy centers (NV -) in diamond have been proposed for high-sensitivity magnetometry and spin-polarization transfer applications.However, surface effects tend to favor and stabilize the less useful neutral form, the NV 0 centers.Here, we report the effects of green laser irradiation on ensembles of nanometer-shallow NV centers in flat and nanostructured diamond surfaces as a function of laser power in a range not previously explored (up to 150 mW/μm 2 ).Fluorescence spectroscopy, optically detected magnetic resonance (ODMR), and charge-photoconversion detection are applied to characterize the properties and dynamics of NV -and NV 0 centers.We demonstrate that high laser power strongly promotes photoconversion of NV 0 to NV -centers.Surprisingly, the excess NV -population is stable over a timescale of 100 ms after switching off the laser, resulting in long-lived enrichment of shallow NV -.The beneficial effect of photoconversion is less marked in nanostructured samples.Our results are important to inform the design of samples and experimental procedures for applications relying on ensembles of shallow NV -centers in diamond.
Ensembles of nitrogen-vacancy (NV) centers in diamond are versatile quantum sensors with broad applications in the physical and life sciences. The concentration of neutral substitutional nitrogen ( [ N s 0 ]) strongly influences NV electronic spin coherence times, sensitivity, and optimal sensing strategies. Diamonds with [ N s 0 ] ∼ 1–10 ppm are a focus of recent material engineering efforts, with higher concentrations being favorable for continuous-wave optically detected magnetic resonance (CW-ODMR) and lower concentrations expected to benefit pulsed magnetometry techniques through extended NV spin coherence times and improved sensing duty cycles. In this work, we synthesize and characterize low- [ N s 0 ] ( ∼ 0.8 ppm), NV-enriched diamond material, engineered through low-strain chemical vapor deposition (CVD) growth on high-quality substrates, 12 C isotopic purification, and controlled electron irradiation and annealing. Our results demonstrate good strain homogeneity in diamonds grown on CVD substrates and spin-bath-limited NV dephasing times. By measuring NV spin and charge properties across a wide range of optical NV excitation intensity, we provide direct comparisons of photon-shot-noise-limited magnetic field sensitivity between the current low- [ N s 0 ] and previously studied higher- [ N s 0 ] ( ∼ 14 ppm) NV-diamond sensors. We show that low- [ N s 0 ] diamond can outperform higher- [ N s 0 ] diamond at moderate and low optical NV excitation intensity. Our results provide practical benchmarks and guidance for selecting NV-diamond sensors tailored to specific experimental constraints and sensing requirements.
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 readout 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 relative distribution of NV centers in a bulk diamond and micro-sized diamonds. For the first time, to the best of our knowledge, ODMR traces of the nitrogen-vacancy center are observed with two-photon excitation, providing a promising tool for fast 3D quantum sensing and imaging.