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Optimization of the coherence properties of diamond samples with an intermediate concentration of NV centers

MetadataDetails
Publication Date2021-01-19
JournalResults in Physics
AuthorsO. R. Rubinas, V.V. Soshenko, S. V. Bolshedvorskii, A. I. Zeleneev, A.S. Galkin
InstitutionsP.N. Lebedev Physical Institute of the Russian Academy of Sciences, Texas A&M University
Citations15
AnalysisFull AI Review Included

This research investigates the optimization of nitrogen-vacancy (NV) center coherence properties in diamond samples characterized by an intermediate concentration of substitutional nitrogen (1017 - 1018 cm-3).

  • Core Challenge Addressed: Increasing NV concentration typically degrades coherence time (T2*) due to nitrogen-related impurities. This work demonstrates compensation for this degradation via optimized postprocessing.
  • Key Achievement (T2*): The dephasing time (T2*) was significantly improved, reaching 0.7 µs at the optimal electron dose, closely approaching the theoretical 13C decoherence limit (approximately 0.9 µs) for natural abundance diamond.
  • Optimal Processing Parameters: An optimal electron irradiation dose of approximately 15 · 1017 cm-2 was identified, maximizing the conversion efficiency of nitrogen donors into NV centers.
  • Sensitivity Enhancement: Optimal postprocessing procedures resulted in an estimated sensitivity improvement of approximately 2 times compared to non-optimal processes for DC magnetometry applications.
  • Conversion Mechanism: The improvement in T2* is achieved by converting substitutional nitrogen donors (C-defects, S=1/2) into NV centers, primarily the neutrally charged NV0 state.
  • Trade-off: While T2* is improved, the conversion process leaves only 15% of the total NV centers in the useful negative charge state (NV-) at the optimal dose, which does not solve the problem of sample absorption.
ParameterValueUnitContext
Investigated Nitrogen Concentration Range1017 - 1018cm-3Substitutional N donors (0.6 - 5.6 ppm)
Optimal Electron Irradiation Dose15 · 1017cm-2Dose maximizing T2* improvement
Electron Irradiation Energy3MeVUsed for vacancy creation
Annealing Temperature800°CPost-irradiation thermal treatment
Maximum Dephasing Time (T2*) Achieved0.7µsAt optimal dose (15·1017 cm-2)
13C Decoherence Limit (T2*)~0.9µsTheoretical limit for natural abundance diamond
Maximum Coherence Time (T2) Observed179.88µsObserved at 4·1017 cm-2 dose
Total NV Center Conversion Saturation (γ)48%Saturation level achieved via fitting model
Useful NV- Fraction (κ) at Optimal Dose15%Fraction of total NV centers in the negative charge state (NV-)
Sensitivity Improvement Factor~2TimesCompared to non-optimal postprocessing for DC magnetometry
NV- Absorption Peak637nmUsed for concentration measurement at -77 K
NV0 Absorption Peak575nmUsed for concentration measurement at -77 K

The study utilized a combination of diamond growth, postprocessing, and advanced spectroscopic techniques:

  1. Diamond Growth: Diamond plates were grown using the low strain High-Pressure High-Temperature (HPHT) technique.
  2. Postprocessing (Irradiation): Samples were irradiated with a 3 MeV electron beam, varying the dose from 2·1017 to 20·1017 cm-2 to control vacancy creation.
  3. Postprocessing (Annealing): All samples were annealed at 800 °C to mobilize vacancies, allowing them to combine with substitutional nitrogen donors to form NV centers.
  4. Substitutional Nitrogen Measurement (nc): Electron Paramagnetic Resonance (EPR) spectroscopy was employed, calibrated using a reference sample measured via Infrared (IR) spectroscopy (specifically the 1130 cm-1 absorption peak).
  5. NV Center Concentration Measurement (nNV- and nNV0): Optical transmission spectroscopy was performed at cryogenic temperature (-77 K) using a Vertex 80v Fourier-transform spectrometer to quantify the concentrations of the negative (NV-) and neutral (NV0) charge states.
  6. Dephasing Time (T2*) Measurement: The T2* time was determined by fitting the decay of Ramsey fringes, implemented using a π/2-τ-π/2 microwave sequence.
  7. Coherence Time (T2) Measurement: The T2 time was measured using the Hahn echo sequence (π/2-τ-π-τ-π/2) under a high magnetic field (~80 Gauss) to mitigate 13C interactions and observe the coherence decay.

The optimization of NV center coherence properties in high-density ensembles is critical for advancing several quantum and classical sensing technologies:

  • Quantum Magnetometry: Enabling high-sensitivity magnetometers, particularly for DC field measurements, where the signal-to-noise ratio is directly tied to the NV concentration and T2*.
  • Magnetic Field Imaging: Used in applications requiring high spatial resolution and sensitivity, such as mapping magnetic fields generated by biological samples or integrated circuits.
  • Solid-State Quantum Information Processing: High-coherence NV ensembles are fundamental components for developing quantum memory and robust solid-state qubits.
  • Gyroscopes and Accelerometers: NV centers are being explored for highly sensitive inertial sensing applications that rely on long spin coherence times.
  • Material Characterization: Utilizing NV ensembles for highly localized sensing of temperature, strain, and electric fields within materials.
  1. 2013 - Nanoscale magnetometry with NV centers in diamond [Crossref]
  2. 2012 - Magnetocardiography with a modular spin-exchange relaxation-free atomic magnetometer array [Crossref]
  3. 2008 - High-sensitivity diamond magnetometer with nanoscale resolution [Crossref]
  4. 2018 - Spin properties of NV centers in high-pressure, high-temperature grown diamond [Crossref]
  5. 2009 - Diamonds with a high density of nitrogen-vacancy centers for magnetometry applications [Crossref]
  6. 2018 - Ultralong Dephasing Times in Solid-State Spin Ensembles via Quantum Control
  7. 2014 - Statistical investigations on nitrogen-vacancy center creation [Crossref]
  8. 2016 - Electron spin decoherence of nitrogen-vacancy center coupled to multiple spin baths [Crossref]
  9. 2011 - Magnetic field imaging with nitrogen-vacancy ensembles [Crossref]