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Exciton-polariton mediated interaction between two nitrogen-vacancy color centers in diamond using two-dimensional transition metal dichalcogenides

MetadataDetails
Publication Date2021-02-04
JournalPhysical review. B./Physical review. B
AuthorsJ. C. G. Henriques, Bruno Amorim, N. M. R. Peres
InstitutionsQuantaLab, University of Minho
Citations5
AnalysisFull AI Review Included
  • Enhanced Quantum Interaction: The study demonstrates a strong, tunable quantum interaction between two negatively charged Nitrogen-Vacancy (NV-) color centers in diamond.
  • Polariton Mediation: This interaction is mediated by Exciton-Polaritons (EPs) propagating in a proximal monolayer of a Transition Metal Dichalcogenide (TMD), such as WS2.
  • Long-Range Coupling: Due to the 2D nature of the polaritons, the NV- coupling (gij) and decay rates (Vij) exhibit a long-range spatial decay proportional to ρ-1/2, which significantly dominates the standard electrostatic dipole-dipole interaction (ρ-3) at distances up to 100 nm.
  • Superradiance Prediction: The model predicts the occurrence of Exciton-Polariton mediated Superradiance (Ī“ > 1) and Subradiance, which are highly sensitive to the NV- separation (ρ) and the orientation of their electric dipole moments.
  • Tunability: Interaction parameters and energy level renormalizations (Lamb shifts Ī”i) are extremely sensitive to the distance between the NV- centers and the TMD layer.
  • General Applicability: The derived quantum master equation framework is applicable to other solid-state emitters, including color centers in hexagonal boron nitride (hBN), facilitating the design of all-van der Waals quantum devices.
ParameterValueUnitContext
NV- Optical Transition Energy (ħω0)1.945eVEnergy difference between the NV- two-levels.
NV- Electric Dipole Moment (µ)1.5DMagnitude used for both dipoles in the optical transition.
TMD Exciton Energy (ħωex)1.94eVTypical A-exciton energy (WS2 parameters used).
Exciton Oscillator Strength (fex)0.39dimensionlessDescribes exciton coupling to the electric field.
Exciton Non-Radiative Decay Rate (γnr)1.99meVLoss rate for the exciton component.
Exciton Dephasing Rate (γd)0.04meVExciton dephasing rate.
TMD Effective Thickness (d)0.65nmThickness of the monolayer TMD.
NV- Energy Renormalization (Ī”i)~25µeVCalculated Lamb shift magnitude.
Polariton Wavelength (Ī»p)~37nmPolariton wavelength at the NV- transition energy (ħω0).
Interaction Decay Profile (gij, Vij)ρ-1/2N/ASpatial decay rate of exciton-polariton mediated coupling (ρ is in-plane separation).
Interaction Dominance Rangeρ > λp/10N/ARange where polariton interaction dominates over ρ-3 dipole-dipole interaction.
Superradiance Condition (Ī“)> 1N/AFigure of merit indicating coherent emission enhancement.
Operating TemperatureLowKParameters (Table I) derived for T = 4 K (WS2).
  1. System Configuration: Modeled two NV- centers (two-level systems) embedded in a diamond slab (dielectric constant ε1) positioned at distances z1 and z2 above a TMD monolayer (at z=0). The TMD rests on a second dielectric (ε2, taken as vacuum).
  2. Hamiltonian Formulation: The system dynamics are described by a modified Dicke Hamiltonian, including terms for the NV- centers (HNV), the TMD exciton-polaritons (Hex-p) modeled as independent bosons, and the dipole coupling interaction (Hint).
  3. TMD Optical Modeling: The TMD optical response is characterized by its frequency-dependent susceptibility χ(ω), which incorporates the exciton resonance (ωex) and intrinsic decay rates (γnr, γd). This susceptibility determines the optical conductivity σ(ω).
  4. Polariton Dispersion Relation: The exciton-polariton energy dispersion (ωq) is solved implicitly using the boundary conditions for the electric field at the TMD interface, requiring the real part of the susceptibility to be negative. An approximate analytical solution (Eq. 13) is used for large momenta (q).
  5. Quantum Master Equation Derivation: The dynamics of the NV- centers’ reduced density matrix ρ(t) are governed by the Lindblad equation, derived by tracing out the exciton-polariton degrees of freedom under the Born-Markov and rotating wave approximations.
  6. Green’s Function Formalism: The resulting effective parameters—Lamb shifts (Ī”i), collective decay rates (Vij), and coupling constants (gij)—are calculated explicitly using the exciton-polariton Green’s functions (retarded/advanced) and the electric field spectral function (Aαβ).
  7. Polariton-Pole Approximation: The exciton-polariton Green’s function is used as a polariton-pole approximation to the full electromagnetic Green’s function, valid when the NV- frequency is close to the polariton frequency and the centers are near the TMD.
  • Scalable Quantum Computing: The strong, long-range (ρ-1/2) polariton-mediated coupling provides a robust mechanism for implementing two-qubit gates and building scalable quantum registers using distant solid-state NV- qubits.
  • Quantum Nanophotonics and Light Sources: Control over collective emission phenomena (Superradiance and Subradiance) allows for the engineering of highly efficient, directional, and fast light emitters or quantum memories integrated into chip-scale devices.
  • Integrated Quantum Devices: The methodology supports the development of quantum optics devices built entirely from van der Waals heterostructures (e.g., hBN emitters coupled via TMDs), offering high integration density and material compatibility.
  • Tunable Quantum Sensors: The extreme sensitivity of the NV- energy shifts and decay rates to the distance and dielectric environment suggests applications in highly localized, tunable quantum sensing and microscopy of 2D materials and interfaces.
  • Solid-State Quantum Networks: The enhanced long-range interaction is critical for linking quantum nodes across a chip, forming the basis for solid-state quantum communication networks.
View Original Abstract

In this paper, starting from a quantum master equation, we discuss the interaction between two negatively charged nitrogen-vacancy color centers in diamond via exciton-polaritons propagating in a two-dimensional transition metal dichalcogenide layer in close proximity to a diamond crystal. We focus on the optical 1.945 eV transition and model the nitrogen-vacancy color centers as two-level (artificial) atoms. We find that the interaction parameters and the energy-level renormalization constants are extremely sensitive to the distance of the nitrogen-vacancy centers to the transition-metal dichalcogenide layer. Analytical expressions are obtained for the spectrum of the exciton-polaritons and for the damping constants entering the Lindblad equation. The conditions for occurrence of exciton mediated superradiance are discussed.

  1. 2017 - Quantum Optics and Nanophotonics