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

Conference on Lasers and Electro-Optics

Spin Coherence in Single NV Centers Coupled to Controllably Assembled Nanopatch Antennas

Simeon Bogdanov, Oksana Makarova, Alexei Lagutchev, Deesha Shah, Chin‐Cheng Chiang, Aleksandr S. Baburin, I. A. Ryzhikov, Soham Saha, Ilya A. Rodionov, Alexandra E. Boltasseva, Vladimir M. Shalaev

Published Jan 1, 2019• 0 citations
Publisher

Abstract

We transfer a pre-characterized nanodiamond with a single nitrogen-vacancy (NV) center onto an epitaxial silver substrate and deterministically couple it to a nanopatch antenna. The NV retains its coherent spin dynamics in this process.
DOI
10.1364/cleo_qels.2019.fm1m.6

Related papers

Spin Coherence in Single NV Centers Coupled to Controllably Assembled Nanopatch Antennas

Simeon Bogdanov, Oksana Makarova, Alexei Lagutchev +8 more

We transfer a pre-characterized nanodiamond with a single nitrogen-vacancy (NV) center onto an epitaxial silver substrate and deterministically couple it to a nanopatch antenna. The NV retains its coherent spin dynamics in this process. © 2019 The Author(s)

Conference on Lasers and Electro-Optics•May 5, 2019•0 citations

Scalable universal quantum gates between nitrogen-vacancy centers in levitated nanodiamond arrays

Guangyu Zhang, Huaijin Zhang, Zhang-qi Yin

Nitrogen-vacancy (NV) centers in nanodiamond offer a promising platform for quantum information processing due to their room-temperature spin coherence and optical addressability. However, scalable quantum processors remain limited by the challenge of achieving strong, controllable interactions between distant NV spins. Here, we propose a scalable architecture utilizing optically levitated nanodiamond arrays, where torsional vibrations mediate the coherent coupling between the embedded NV centers. By optimizing the shape of ellipsoidal nanoparticles, we achieve a light-induced coupling strength exceeding 119 kHz between torsional modes of the distant levitated nanodiamonds, which are two orders of magnitude larger than the typical decoherence rates in this system. This strong interaction, combined with magnetic-field-enabled spin-torsion coupling, establishes an effective interaction between the spatially separated NV centers in the distant nanodiamonds. Numerical simulations confirm that dynamic decoupling can suppress both thermal noise and spin dephasing, enabling two-qubit gates with fidelity exceeding 99%. This work provides a foundation for reconfigurable quantum hybrid systems, with potential applications in rotational sensing and programmable quantum processing.

arXiv:2504.08194•Physical Review A•Aug 11, 2025•1 citation

Three-dimensional localization of spins in diamond using 12C implantation

Kenichi Ohno, F. Joseph Heremans, Charles F. de las Casas +4 more

We demonstrate three-dimensional localization of a single nitrogen-vacancy (NV) center in diamond by combining nitrogen doping during growth with a post-growth 12C implantation technique that facilitates vacancy formation in the crystal. We show that the NV density can be controlled by the implantation dose without necessitating increase of the nitrogen incorporation. By implanting a large 12C dose through nanoscale apertures, we can localize an individual NV center within a volume of (∼180 nm)3 at a deterministic position while repeatedly preserving a coherence time (T2) > 300 μs. This deterministic position control of coherent NV centers enables integration into NV-based nanostructures to realize scalable spin-sensing devices as well as coherent spin coupling mediated by photons and phonons.

arXiv:1405.7352•Applied Physics Letters•Aug 4, 2014•72 citations

Coupling of nitrogen-vacancy centers in a nanodiamond to a silver nanocube

Sebastain K.H. Andersen, Shailesh Kumar, Sergey I. Bozhevolnyi

Spontaneous emission (SE) of nitrogen-vacancy centers (NV-centers), which are contained in a single nanodiamond (ND), placed near a silver nanocube, is investigated both experimentally and theoretically. The ND-cube system is assembled with an atomic force microscope, allowing us to directly compare its SE properties to that of the isolated ND. It is demonstrated that the cube coupled NV-centers exhibit strongly polarized SE. For optimal pump laser polarization, the rate of photons is enhanced by a factor of 4.1, with the excited state lifetime being reduced by a factor of 4.1. The enhancement of photon rate is a consequence of local field enhancement of the pump laser, while the SE polarization and lifetime reduction results from coupling of NV-centers to the localized surface plasmon mode of the nanocube. The experimental observations are in qualitative agreement with the model of SE from randomly oriented electric dipoles, allowing us to reveal the underlying physics of the investigated configuration.

Optical Materials Express•Oct 5, 2016•18 citations

Deterministic fabrication of dielectric loaded waveguides coupled to single nitrogen vacancy centers in nanodiamonds

Hamidreza Siampour, Shailesh Kumar, Sergey I. Bozhevolnyi

We report on the fabrication of dielectric-loaded-waveguides which are excited by single-nitrogen-vacancy (NV) centers in nanodiamonds. The waveguides are deterministically written onto the pre-characterized nanodiamonds by using electron beam lithography of hydrogen silsesquioxane (HSQ) resist on silver-coated silicon substrate. Change in lifetime for NV-centers is observed after fabrication of waveguides and an antibunching in correlation measurement confirms that nanodiamonds contain single NV-centers.

•Jan 4, 2017•0 citations

Ultrabright Linearly Polarized Photon Generation from a Nitrogen Vacancy Center in a Nanocube Dimer Antenna

Sebastian K. H. Andersen, Shailesh Kumar, Sergey I. Bozhevolnyi

We demonstrate an exceptionally bright photon source based on a single nitrogen-vacancy center (NV center) in a nanodiamond (ND) placed in the nanoscale gap between two monocrystalline silver cubes in a dimer configuration. The system is operated near saturation at a stable photon rate of 850 kcps, while we further achieve strongly polarized emission and high single photon purity, evident by the measured autocorrelation with a g (2) (0) value of 0.08. These photon source features are key parameters for quantum technological applications, such as secure communication based on quantum key distribution. The cube antenna is assembled with an atomic force microscope, which allows us to predetermine the dipole orientation of the NV center and optimize cube positioning accordingly, while also tracking the evolution of emission parameters from isolated ND to the one- and two-cube configuration. The experiment is well described by finite element modeling, assuming an instrinsic quantum efficiency of 0.35. We attribute the large photon rate of the assembled photon source, to increased quantum efficiency of the NV center and high antenna efficiency.

arXiv:1706.09874•Nano Letters•May 4, 2017•87 citations
Nitrogen-vacancy (NV) centers in nanodiamond offer a promising platform for quantum information processing due to their room-temperature spin coherence and optical addressability. However, scalable quantum processors remain limited by the challenge of achieving strong, controllable interactions between distant NV spins. Here, we propose a scalable architecture utilizing optically levitated nanodiamond arrays, where torsional vibrations mediate the coherent coupling between the embedded NV centers. By optimizing the shape of ellipsoidal nanoparticles, we achieve a light-induced coupling strength exceeding 119 kHz between torsional modes of the distant levitated nanodiamonds, which are two orders of magnitude larger than the typical decoherence rates in this system. This strong interaction, combined with magnetic-field-enabled spin-torsion coupling, establishes an effective interaction between the spatially separated NV centers in the distant nanodiamonds. Numerical simulations confirm that dynamic decoupling can suppress both thermal noise and spin dephasing, enabling two-qubit gates with fidelity exceeding 99%. This work provides a foundation for reconfigurable quantum hybrid systems, with potential applications in rotational sensing and programmable quantum processing.
We demonstrate three-dimensional localization of a single nitrogen-vacancy (NV) center in diamond by combining nitrogen doping during growth with a post-growth 12C implantation technique that facilitates vacancy formation in the crystal. We show that the NV density can be controlled by the implantation dose without necessitating increase of the nitrogen incorporation. By implanting a large 12C dose through nanoscale apertures, we can localize an individual NV center within a volume of (∼180 nm)3 at a deterministic position while repeatedly preserving a coherence time (T2) > 300 μs. This deterministic position control of coherent NV centers enables integration into NV-based nanostructures to realize scalable spin-sensing devices as well as coherent spin coupling mediated by photons and phonons.
Spontaneous emission (SE) of nitrogen-vacancy centers (NV-centers), which are contained in a single nanodiamond (ND), placed near a silver nanocube, is investigated both experimentally and theoretically. The ND-cube system is assembled with an atomic force microscope, allowing us to directly compare its SE properties to that of the isolated ND. It is demonstrated that the cube coupled NV-centers exhibit strongly polarized SE. For optimal pump laser polarization, the rate of photons is enhanced by a factor of 4.1, with the excited state lifetime being reduced by a factor of 4.1. The enhancement of photon rate is a consequence of local field enhancement of the pump laser, while the SE polarization and lifetime reduction results from coupling of NV-centers to the localized surface plasmon mode of the nanocube. The experimental observations are in qualitative agreement with the model of SE from randomly oriented electric dipoles, allowing us to reveal the underlying physics of the investigated configuration.
We report on the fabrication of dielectric-loaded-waveguides which are excited by single-nitrogen-vacancy (NV) centers in nanodiamonds. The waveguides are deterministically written onto the pre-characterized nanodiamonds by using electron beam lithography of hydrogen silsesquioxane (HSQ) resist on silver-coated silicon substrate. Change in lifetime for NV-centers is observed after fabrication of waveguides and an antibunching in correlation measurement confirms that nanodiamonds contain single NV-centers.
We demonstrate an exceptionally bright photon source based on a single nitrogen-vacancy center (NV center) in a nanodiamond (ND) placed in the nanoscale gap between two monocrystalline silver cubes in a dimer configuration. The system is operated near saturation at a stable photon rate of 850 kcps, while we further achieve strongly polarized emission and high single photon purity, evident by the measured autocorrelation with a g (2) (0) value of 0.08. These photon source features are key parameters for quantum technological applications, such as secure communication based on quantum key distribution. The cube antenna is assembled with an atomic force microscope, which allows us to predetermine the dipole orientation of the NV center and optimize cube positioning accordingly, while also tracking the evolution of emission parameters from isolated ND to the one- and two-cube configuration. The experiment is well described by finite element modeling, assuming an instrinsic quantum efficiency of 0.35. We attribute the large photon rate of the assembled photon source, to increased quantum efficiency of the NV center and high antenna efficiency.