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Measurement of the excited-state transverse hyperfine coupling in NV centers via dynamic nuclear polarization

MetadataDetails
Publication Date2016-12-14
JournalDSpace@MIT (Massachusetts Institute of Technology)
AuthorsFrancesco Poggiali, Nicole Fabbri, Paola Cappellaro
Citations3
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Technical Analysis and Documentation: NV Center Quantum Sensing Platforms

Section titled “Technical Analysis and Documentation: NV Center Quantum Sensing Platforms”

This documentation analyzes the methods and requirements detailed in “Measurement of the excited-state transverse hyperfine coupling in NV centers via dynamic nuclear polarization” (Poggiali et al., 2017) and connects them directly to the advanced MPCVD diamond solutions available through 6CCVD.


The research successfully characterized a critical parameter for Nitrogen-Vacancy (NV) center quantum control, directly enabling enhanced initialization and operation of nuclear spin qubits.

  • Core Achievement: First direct experimental measurement of the excited-state transverse hyperfine coupling ($C_{\perp}$) between the NV electronic spin and the substitutional 14N nuclear spin.
  • Resulting Parameter: $C_{\perp}$ was precisely determined as $(-23 \pm 3)$ MHz, significantly deviating from prior theoretical assumptions of isotropic coupling.
  • Methodological Breakthrough: The determination relies on precisely monitoring the transient behavior of Dynamic Nuclear Polarization (DNP) near the Excited State Level Anti-Crossing (ESLAC).
  • Material Requirement: The experiment necessitated extremely high-purity, low-strain Electronic Grade Single Crystal Diamond (SCD) with minimal nitrogen background (< 5 ppb 14N) to isolate single NV centers.
  • Application Relevance: Accurate knowledge of $C_{\perp}$ is vital for optimizing protocols requiring fast and highly accurate control of nuclear spins, accelerating progress in quantum computing, enhanced NMR, and quantum sensing applications.
  • 6CCVD Value Proposition: 6CCVD provides the necessary Electronic Grade SCD substrates, offering unmatched purity control, custom crystal orientation, and specialized processing (metalization, polishing) required for scaling similar quantum hardware.

The following critical parameters and hard data points were extracted from the study detailing the NV spin system and experimental conditions.

ParameterValueUnitContext
Measured Transverse Coupling (C⊥)-23 $\pm$ 3MHzExcited-state 14N hyperfine coupling
Ground State Zero-Field Splitting (Dg)2.87GHzUsed for Hamiltonian model
Excited State Zero-Field Splitting (De)1.42GHzUsed for Hamiltonian model
Nuclear Quadrupole Interaction (Q)-4.945MHz14N nucleus
ESLAC Magnetic Field (B)$\approx 510$GLocation of Excited State Level Anti-Crossing
Operating Magnetic Field Range200 to 420GApplied external field B
NV Center Nitrogen Concentration (14N)< 5ppbRequired for electronic grade bulk diamond
Optical Excitation Wavelength532nmSpin polarization laser
Ramsey MW Pulse Duration25 - 50nsUsed to drive electronic spin transitions
DNP Characteristic Time Constant ($\tau$)1 to 5$\mu$sTime scale of nuclear polarization process

The determination of the excited-state transverse hyperfine coupling relies on controlling the NV center’s environment and utilizing highly precise spin manipulation sequences, necessitating robust material properties.

  1. High-Purity Material Sourcing: Experiments were performed on electronic grade bulk diamond with natural 1.1% 13C abundance and extremely low nitrogen concentration (< 5 ppb) to ensure the isolation of single NV centers free from proximal spin noise.
  2. Spin Initialization: The NV electronic spin (S=1) was polarized to the ms = 0 ground state sublevel via continuous 532 nm optical pumping (Green Laser).
  3. Dynamic Nuclear Polarization (DNP) Induction: The system was subjected to optical pumping for variable durations (0.5 $\mu$s to 17.5 $\mu$s) while precisely tuned to magnetic fields (200 G to 420 G) near the ESLAC ($\approx 510$ G).
  4. Spin Control and Readout: Ramsey spectroscopy involving microwave ($\pi$/2 pulses) and radiofrequency ($\pi$ pulses) driving was used to coherently manipulate the electronic and 14N nuclear spins.
  5. Hyperfine Population Measurement: Fourier analysis of the Ramsey signal components yielded the relative probability (PmI) of the three 14N nuclear spin projections ($m_{I} = 0, \pm 1$).
  6. Data Modeling: The time evolution of $P_{+1}$ was compared against a numerical simulation derived from the generalized Liouville master equation to extract the unknown transverse coupling $C_{\perp}$ as the only adjustable parameter.

6CCVD is an expert provider of MPCVD diamond necessary to replicate, optimize, and scale this advanced quantum research. Our ability to control material purity, crystal dimensions, and surface functionalization directly addresses the stringent requirements of NV center platforms.

The precise measurement of the excited-state Hamiltonian requires high-purity, low-strain diamond with controlled defect density.

Research Requirement6CCVD Material SolutionTechnical Advantage
Isolation of Single NVsElectronic Grade Single Crystal Diamond (SCD)Ultra-low [N] concentration (< 1 ppb unintentional, down to 5 ppb intentional) for high-fidelity qubits.
High Resolution DNPIsotopically Pure SCD (12C)Reduces background spin noise from 13C (natural abundance is 1.1%), leading to significantly enhanced T2 coherence times and improved spectral resolution.
Potential for ScalingOptical Grade Polycrystalline Diamond (PCD)Available in large area wafers (up to 125mm) for high-throughput screening and integration into commercial devices.
Bulk IntegrationCustom Substrate ThicknessesSCD plates available up to 500 $\mu$m thick, allowing deep-bulk NV implantation or controlled surface NV generation.

The integration of NV quantum platforms often demands specialized physical and electrical interfaces. 6CCVD supports the full transition from fundamental research to integrated devices.

  • Precision Polishing: To enable high-fidelity optical addressing via confocal microscopy, 6CCVD guarantees ultra-smooth surfaces, providing Ra < 1 nm on SCD wafers and Ra < 5 nm on inch-sized PCD wafers.
  • Custom Metalization Schemes: The experimental setup utilized a wire antenna for MW/RF delivery. For on-chip integration, 6CCVD offers internal capabilities for depositing custom metal films (Au, Pt, Pd, Ti, W, Cu) for lithographically defined microwave guides (CPWs) and electrodes.
  • Custom Dimensions and Orientation: SCD wafers can be supplied in custom dimensions and specific crystallographic orientations (e.g., [111] required for magnetic field alignment) tailored to bespoke quantum experiments.

This research demonstrates the necessity of high-precision materials engineering to extract fundamental physics data.

  • Material Selection Expertise: 6CCVD’s in-house PhD team provides consultative support for engineers and scientists. We specialize in assisting with NV center material design, ensuring optimal [N] concentration, isotopic purity, and substrate characteristics needed for similar Dynamic Nuclear Polarization (DNP) or Quantum Sensing projects.
  • Global Logistics: We ensure reliable global supply chain management with flexible shipping options (DDU default, DDP available) to deliver high-value diamond materials worldwide.

For custom specifications or material consultation, visit 6ccvd.com or contact our engineering team directly.

View Original Abstract

Precise knowledge of a quantum system’s Hamiltonian is a critical pre-requisite for its use in many quantum information technologies. Here, we report a method for the precise characterization of the non-secular part of the excited-state Hamiltonian of an electronic-nuclear spin system in diamond. The method relies on the investigation of the dynamic nuclear polarization mediated by the electronic spin, which is currently exploited as a primary tool for initializing nuclear qubits and performing enhanced nuclear magnetic resonance. By measuring the temporal evolution of the population of the ground-state hyperfine levels of a nitrogen-vacancy center, we obtain the first direct estimation of the excited-state transverse hyperfine coupling between its electronic and nitrogen nuclear spin. Our method could also be applied to other electron-nuclear spin systems, such as those related to defects in silicon carbide.