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Proposed rapid detection of nuclear spins with entanglement-enhancedn sensors

MetadataDetails
Publication Date2021-05-07
JournalarXiv (Cornell University)
AuthorsHideaki Hakoshima, Yuichiro Matsuzaki, T. Ishikawa
InstitutionsNational Institute of Advanced Industrial Science and Technology
AnalysisFull AI Review Included

This research proposes and theoretically validates a method for drastically accelerating Nuclear Magnetic Resonance (NMR) detection of distant nuclear spins using entangled Nitrogen-Vacancy (NV) centers in diamond.

  • Core Value Proposition: Overcomes the fundamental limitation of conventional NV-NMR, where the dipole-dipole interaction (scaling as r-3) makes detecting distant nuclear spins prohibitively slow.
  • Speed Enhancement: The proposed entanglement-enhanced protocol reduces the minimum detectable time by up to 107 times compared to conventional sensing using separable NV centers.
  • Mechanism: The enhancement is achieved by preparing the NV center probes in a highly entangled GHZ (Greenberger-Horne-Zeilinger) state, rather than separable states.
  • Application Range: This rapid detection capability is crucial when the distance between the NV sensor layer and the target nuclear spins (zmin) is large, specifically hundreds of nanometers (e.g., 1 µm).
  • Target State: The protocol is designed for detecting unpolarized nuclear spin ensembles, which is the standard assumption for room-temperature NMR.
  • Impact: Paves the way for practical, nanoscale NMR spectroscopy of distant targets, enabling new applications in material science and biology.

The following specifications are derived from the theoretical modeling comparing the conventional (separable) and proposed (GHZ) protocols.

ParameterValueUnitContext
Time Reduction Factor~107FactorAchieved at zmin = 1 µm (using NV1 parameters)
Minimum Detectable Time (Separable)~109sTime required to detect spins at zmin ≄ 500 nm
Minimum Detectable Time (GHZ, NV1)~60sTime required to detect spins at zmin = 1 µm
Dipole Interaction Scalingr-3N/ARate of decrease of coupling strength with distance (r)
Target Spin StateCompletely MixedN/AUnpolarized nuclear spin ensemble (M spins)
Probe Spin StateGHZ StateN/AEntangled state used for enhanced sensing (L NV centers)
Nuclear Spin Density (Protons)1.0 x 1022cm-3Density of the target ensemble
NV Center Density (NV1)1.1 x 1017cm-3Probe density (ρNV) used in modeling
NV Center Coherence Time (NV3)3.1 x 10-4sT2echo used for high-performance NV center modeling

The study employs theoretical modeling and perturbation analysis to compare two distinct protocols for detecting unpolarized nuclear spin ensembles (M spins) using L NV center probes.

  1. System Setup: The NV centers (probes) are modeled as being uniformly distributed within a semicylindrical volume, sensing nuclear spins located at a minimum distance zmin. The interaction is governed by the Zeeman and dipole-dipole Hamiltonian.
  2. Conventional Protocol (Separable States):
    • Probe State: Initialized in separable states (e.g., |+> āŠ— |+> …).
    • Sequence: Utilizes Periodic Dynamical Decoupling (PDD) sequences (NDD repetitions of evolution and Ļ€-pulses) to maximize signal coherence.
    • Metric: The minimum detectable time T(DD) is calculated by optimizing the interaction time (Ļ„) and the number of repetitions (NDD) to achieve a Signal-to-Noise Ratio (SNR) ≄ 1.
  3. Proposed Protocol (GHZ State):
    • Probe State: Initialized in a highly entangled GHZ state (e.g., (|00…0> + |11…1>)/√2).
    • Sequence: Uses a simple spin echo sequence (equivalent to PDD with NDD = 1). The total sequence involves evolution (Ļ„), Ļ€-pulse, evolution (Ļ„), and a second Ļ€-pulse.
    • Metric: The measurement probability p(GHZ) is calculated, and the minimum detectable time T(ent) is determined when the SNR ≄ 1.
  4. Analysis: The expectation values and variances for both protocols are derived using second-order perturbation formulas, incorporating the effects of NV center dephasing (T2echo).
  5. Optimization: Numerical optimization is performed on geometric factors (rmax, zmax) and interaction parameters (Ļ„, ω) to find the absolute minimum detectable time for both separable and GHZ protocols across varying zmin.

The development of rapid, entanglement-enhanced nanoscale NMR spectroscopy using NV centers has significant implications across several high-tech sectors:

  • Quantum Sensing and Metrology: Provides a practical demonstration of using quantum entanglement (GHZ states) to surpass the Standard Quantum Limit (SQL) in real-world sensing applications, enhancing magnetic field sensitivity.
  • Nanoscale NMR Spectroscopy: Enables chemical and structural analysis of extremely small sample volumes (micro- and nanometer scales) or thin films where the target spins are physically separated from the sensor layer.
  • Biological Imaging: Allows for the rapid detection and characterization of spin ensembles in distant biological structures, potentially improving the speed and resolution of NV-based bio-sensing.
  • Material Science: Facilitates the analysis of spin dynamics and chemical composition at interfaces or surfaces where the NV centers are embedded in a diamond substrate, and the target material is deposited hundreds of nanometers away.
  • Diamond Quantum Devices: Drives requirements for manufacturing high-quality diamond substrates with precisely controlled, high-density NV center ensembles capable of maintaining long coherence times (T2echo) necessary for entanglement protocols.
View Original Abstract

Recently, there have been significant developments to detect nuclear spins\nwith an nitrogen vacancy (NV) center in diamond. However, due to the nature of\nthe short range dipole-dipole interaction, it takes a long time to detect\ndistant nuclear spins with the NV centers. Here, we propose a rapid detection\nof nuclear spins with an entanglement between the NV centers. We show that the\nnecessary time to detect the nuclear spins with the entanglement is several\norders of magnitude shorter than that with separable NV centers. Our result\npave the way for new applications in nanoscale nuclear magnetic resonance\nspectroscopy.\n