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

arXiv:1908.01591 · New Journal of Physics

Preparing single SiV − center in nanodiamonds for external, optical coupling with access to all degrees of freedom

Stefan Häußler, Lukas Hartung, Konstantin G. Fehler, Lukas Antoniuk, L. F. Kulikova, Валерий Александрович Давыдов, V. Agafonov, Fedor Jelezko, Alexander Kubanek

Published Oct 1, 2019• 21 citations
arXivHTMLPDF

Abstract

Abstract Optical coupling enables intermediate- and long-range interactions between distant quantum emitters. Such interaction may be the basic element in bottom-up approaches of coupled spin systems or for integrated quantum photonics and quantum plasmonics. Here, we prepare nanodiamonds carrying single, negatively-charged silicon-vacancy centers for evanescent optical coupling with access to all degrees of freedom by means of atomic force nanomanipulation. The color centers feature excellent optical properties, comparable to silicon-vacancy centers in bulk diamond, resulting in a resolvable fine structure splitting, a linewidth close to the Fourier-Transform limit under resonant excitation and a good polarization contrast. We determine the orbital relaxation time T 1 of the orbitally split ground states and show that all optical properties are conserved during translational nanomanipulation. Furthermore, we demonstrate the rotation of the nanodiamonds. In contrast to the translational operation, the rotation leads to a change in polarization contrast. We utilize the change in polarization contrast before and after nanomanipulation to determine the rotation angle. Finally, we evaluate the likelihood for indistinguishable, single photon emission of silicon-vacancy centers located in different nanodiamonds. Our work enables ideal evanescent, optical coupling of distant nanodiamonds containing silicon-vacancy centers with applications in the realization of quantum networks, quantum repeaters or complex quantum systems.

DOI
10.1088/1367-2630/ab4cf7

Related papers

Strongly Coupled Spins of Silicon-Vacancy Centers Inside a Nanodiamond with Sub-Megahertz Linewidth

Marco Klotz, Richard Waltrich, Niklas Lettner +2 more

The search for long-lived quantum memories, which can be efficiently interfaced with flying qubits is longstanding. One possible solution is to use the electron spin of a color center in diamond to mediate interaction between a long-lived nuclear spin and a photon. Realizing this in a nanodiamond furthermore facilitates the integration into photonic devices and enables the realization of hybrid quantum systems with access to quantum memories. Here, we investigated the spin environment of negatively-charged Silicon-Vacancy centers in a nanodiamond and demonstrate strong coupling of its electron spin, while the electron spin's decoherence rate remained below 1 MHz. We furthermore demonstrate multi-spin coupling with the potential to establish registers of quantum memories in nanodiamonds.

arXiv:2312.08967•Dec 14, 2023•0 citations

Two-Photon Interference from Silicon-Vacancy Centers in Remote Nanodiamonds

Richard Waltrich, Marco Klotz, V. Agafonov +1 more

The generation of indistinguishable photons is a key requirement for solid-state quantum emitters as a viable source for applications in quantum technologies. Restricting the dimensions of the solid-state host to a size well below the wavelength of light emitted by a defect-center enables efficient external optical coupling, for example for hybrid integration into photonic devices. However, stringent restrictions on the host dimensions result in severe limitations on the spectral properties reducing the indistinguishability of emitted photons. Here, we demonstrate two-photon interference from two negatively-charged Silicon-Vacancy centers located in remote nanodiamonds. The Hong-Ou-Mandel interference efficiency reaches 61% with a coalescence time window of 0.35 ns. We furthermore show a high yield of pairs of Silicon-Vacancy centers with indistinguishable optical transitions. Therefore, our work opens new paths in hybrid quantum technology based on indistinguishable single-photon emitters in nanodiamonds.

arXiv:2306.10524•Jun 18, 2023•0 citations

Evaluation of single silicon vacancy centers in nanodiamonds created by ion implantation at cryogenic temperatures

Konosuke Shimazaki, Kazuki Suzuki, Kengo Sakamoto +5 more

Abstract Silicon vacancy (SiV) centers in diamonds have attracted much attention because of their stability and narrow emission linewidth, and are promising for applications in quantum information technology. SiV-center-encapsulated nanodiamonds have also attracted much attention because of their potential to be coupled to various photonic devices. One efficient way to fabricate nanodiamonds that contain SiV centers is Si ion implantation into nanodiamonds. However, the evaluation of a single SiV center in a nanodiamond produced by this method at low temperatures has not been performed. In this study, we report on the optical properties of a single SiV center in a nanodiamond produced by ion implantation at cryogenic temperatures. The emission spectrum from a single SiV center ( g 2 ( 0 ) = 0.19 ) was observed with four distinct fine splittings of the zero-phonon line (ZPL) at 4 K. At an excitation power of 50 μ W, the full width at half maximum of the ZPL reached the spectrometer resolution limit (0.09 nm). The temperature dependence of the emission peak is consistent with that of the emission coming from an SiV center under high strain. The results obtained in this work suggest that nanodiamonds containing single SiV centers formed using this method will be an important building block for the realization of quantum information applications.

New Journal of Physics•Sep 1, 2024•5 citations

Optical driving, spin initialization and readout of single SiV− centers in a Fabry-Perot resonator

Gregor W. Bayer, Robert Berghaus, Selene Sachero +8 more

Abstract Large-scale quantum communication networks require quantum repeaters due to the signal attenuation in optical fibers. Ideal quantum repeater nodes efficiently link a quantum memory with photons serving as flying qubits. Color centers in diamond, particularly the negatively charged silicon vacancy center, are promising candidates to establish such nodes. Inefficient connection between the color center’s spin to the optical fiber networks is a major obstacle, that could be resolved by utilizing optical resonators. Here, we couple individual silicon vacancy centers incorporated in a nanodiamond to a hemispherical, stable Fabry-Perot microcavity, achieving Purcell-factors larger than 1. We demonstrate coherent optical driving between ground and excited state with a Rabi-frequency of 330 MHz, all-optical initialization and readout of the electron spin in magnetic fields of up to 3.2 T. Spin initialization within 67 ns with a 80 % fidelity and a lifetime of 350 ns are reached. Our demonstration opens the way to realize quantum repeater applications.

Communications Physics•Oct 16, 2023•25 citations

An integrated diamond nanophotonics platform for quantum optics

Ruffin E. Evans, Денис Дмитриевич Сукачев, Christian N. Nguyen +7 more

Efficient interfaces between optical photons and quantum bits are fundamental building blocks for quantum networks and large-scale quantum computers. We demonstrate an integrated platform for scalable quantum optics based on color centers coupled to diamond nanodevices. First, we incorporate nitrogen-vacancy (NV) centers in diamond into hybrid nanophotonic crystal cavities. Despite our progress towards coupling the NV to cavity photons, we find that the NV-cavity interface is limited by the imperfections of the color center's properties and its local environment. We approach this challenge first by characterizing and modifying the diamond surface to reduce the environmental noise affecting the NV optical transition. Subsequently, we develop a new approach that makes use of a quantum emitter with intrinsic protection from this noise: the silicon-vacancy (SiV) center in diamond. We demonstrate that SiV centers introduced through ion implantation feature highly coherent optical transitions, even inside nanostructures. By placing SiV centers inside all-diamond photonic crystal cavities, we achieve strong SiV-photon coupling with a cooperativity of greater than 20. Using this platform, we realize a quantum-optical switch controlled by the spin degree of freedom of a single SiV. By measuring intensity correlations of indistinguishable Raman photons emitted into a single waveguide, we observe a quantum interference effect resulting from the superradiant emission of two probabilistically entangled SiV centers. Finally, we demonstrate controllable photon-mediated interactions between the spin degrees of freedom of two cavity-coupled SiV centers. When the optical transitions of the two SiV centers are tuned into resonance, the coupling of each SiV to the common cavity mode results in a coherent interaction between the two SiVs, leading to the observation of super- and sub-radiant two-SiV states.

Bulletin of the American Physical Society•Mar 9, 2018•0 citations

Tunable cavity coupling of a single Sn - V − center in nanodiamond across the bad-emitter and bad-cavity regimes

Selene Sachero, Robert Berghaus, Florian Feuchtmayr +5 more

Efficient coupling between quantum emitters and optical cavities is essential for scalable quantum photonic technologies. Group-IV vacancy centers in diamond, particularly the negatively charged tin-vacancy center, have emerged as promising candidates due to their spectral stability, high Debye-Waller factor, and large orbital splitting in ground states. Here, we demonstrate controlled coupling of a single negatively charged tin-vacancy center hosted in a nanodiamond to a fully tunable Fabry-Pérot microcavity. At cryogenic temperatures, we access the weak-coupling regime and observe a transition from the bad-emitter regime to the bad-cavity regime as the optical transition of the color center narrows. At 4 K, a Purcell factor exceeding 1.7 is measured, confirming cavity-enhanced emission. The obtained results demonstrate the potential of Sn − V − centers in nanodiamonds as a coherent single-photon source for quantum networks.

arXiv:2507.06553•Physical Review Applied•Nov 20, 2025•0 citations
Abstract Optical coupling enables intermediate- and long-range interactions between distant quantum emitters. Such interaction may be the basic element in bottom-up approaches of coupled spin systems or for integrated quantum photonics and quantum plasmonics. Here, we prepare nanodiamonds carrying single, negatively-charged silicon-vacancy centers for evanescent optical coupling with access to all degrees of freedom by means of atomic force nanomanipulation. The color centers feature excellent optical properties, comparable to silicon-vacancy centers in bulk diamond, resulting in a resolvable fine structure splitting, a linewidth close to the Fourier-Transform limit under resonant excitation and a good polarization contrast. We determine the orbital relaxation time T 1 of the orbitally split ground states and show that all optical properties are conserved during translational nanomanipulation. Furthermore, we demonstrate the rotation of the nanodiamonds. In contrast to the translational operation, the rotation leads to a change in polarization contrast. We utilize the change in polarization contrast before and after nanomanipulation to determine the rotation angle. Finally, we evaluate the likelihood for indistinguishable, single photon emission of silicon-vacancy centers located in different nanodiamonds. Our work enables ideal evanescent, optical coupling of distant nanodiamonds containing silicon-vacancy centers with applications in the realization of quantum networks, quantum repeaters or complex quantum systems.
The search for long-lived quantum memories, which can be efficiently interfaced with flying qubits is longstanding. One possible solution is to use the electron spin of a color center in diamond to mediate interaction between a long-lived nuclear spin and a photon. Realizing this in a nanodiamond furthermore facilitates the integration into photonic devices and enables the realization of hybrid quantum systems with access to quantum memories. Here, we investigated the spin environment of negatively-charged Silicon-Vacancy centers in a nanodiamond and demonstrate strong coupling of its electron spin, while the electron spin's decoherence rate remained below 1 MHz. We furthermore demonstrate multi-spin coupling with the potential to establish registers of quantum memories in nanodiamonds.
The generation of indistinguishable photons is a key requirement for solid-state quantum emitters as a viable source for applications in quantum technologies. Restricting the dimensions of the solid-state host to a size well below the wavelength of light emitted by a defect-center enables efficient external optical coupling, for example for hybrid integration into photonic devices. However, stringent restrictions on the host dimensions result in severe limitations on the spectral properties reducing the indistinguishability of emitted photons. Here, we demonstrate two-photon interference from two negatively-charged Silicon-Vacancy centers located in remote nanodiamonds. The Hong-Ou-Mandel interference efficiency reaches 61% with a coalescence time window of 0.35 ns. We furthermore show a high yield of pairs of Silicon-Vacancy centers with indistinguishable optical transitions. Therefore, our work opens new paths in hybrid quantum technology based on indistinguishable single-photon emitters in nanodiamonds.
Abstract Silicon vacancy (SiV) centers in diamonds have attracted much attention because of their stability and narrow emission linewidth, and are promising for applications in quantum information technology. SiV-center-encapsulated nanodiamonds have also attracted much attention because of their potential to be coupled to various photonic devices. One efficient way to fabricate nanodiamonds that contain SiV centers is Si ion implantation into nanodiamonds. However, the evaluation of a single SiV center in a nanodiamond produced by this method at low temperatures has not been performed. In this study, we report on the optical properties of a single SiV center in a nanodiamond produced by ion implantation at cryogenic temperatures. The emission spectrum from a single SiV center ( g 2 ( 0 ) = 0.19 ) was observed with four distinct fine splittings of the zero-phonon line (ZPL) at 4 K. At an excitation power of 50 μ W, the full width at half maximum of the ZPL reached the spectrometer resolution limit (0.09 nm). The temperature dependence of the emission peak is consistent with that of the emission coming from an SiV center under high strain. The results obtained in this work suggest that nanodiamonds containing single SiV centers formed using this method will be an important building block for the realization of quantum information applications.
Abstract Large-scale quantum communication networks require quantum repeaters due to the signal attenuation in optical fibers. Ideal quantum repeater nodes efficiently link a quantum memory with photons serving as flying qubits. Color centers in diamond, particularly the negatively charged silicon vacancy center, are promising candidates to establish such nodes. Inefficient connection between the color center’s spin to the optical fiber networks is a major obstacle, that could be resolved by utilizing optical resonators. Here, we couple individual silicon vacancy centers incorporated in a nanodiamond to a hemispherical, stable Fabry-Perot microcavity, achieving Purcell-factors larger than 1. We demonstrate coherent optical driving between ground and excited state with a Rabi-frequency of 330 MHz, all-optical initialization and readout of the electron spin in magnetic fields of up to 3.2 T. Spin initialization within 67 ns with a 80 % fidelity and a lifetime of 350 ns are reached. Our demonstration opens the way to realize quantum repeater applications.
Efficient interfaces between optical photons and quantum bits are fundamental building blocks for quantum networks and large-scale quantum computers. We demonstrate an integrated platform for scalable quantum optics based on color centers coupled to diamond nanodevices. First, we incorporate nitrogen-vacancy (NV) centers in diamond into hybrid nanophotonic crystal cavities. Despite our progress towards coupling the NV to cavity photons, we find that the NV-cavity interface is limited by the imperfections of the color center's properties and its local environment. We approach this challenge first by characterizing and modifying the diamond surface to reduce the environmental noise affecting the NV optical transition. Subsequently, we develop a new approach that makes use of a quantum emitter with intrinsic protection from this noise: the silicon-vacancy (SiV) center in diamond. We demonstrate that SiV centers introduced through ion implantation feature highly coherent optical transitions, even inside nanostructures. By placing SiV centers inside all-diamond photonic crystal cavities, we achieve strong SiV-photon coupling with a cooperativity of greater than 20. Using this platform, we realize a quantum-optical switch controlled by the spin degree of freedom of a single SiV. By measuring intensity correlations of indistinguishable Raman photons emitted into a single waveguide, we observe a quantum interference effect resulting from the superradiant emission of two probabilistically entangled SiV centers. Finally, we demonstrate controllable photon-mediated interactions between the spin degrees of freedom of two cavity-coupled SiV centers. When the optical transitions of the two SiV centers are tuned into resonance, the coupling of each SiV to the common cavity mode results in a coherent interaction between the two SiVs, leading to the observation of super- and sub-radiant two-SiV states.
Efficient coupling between quantum emitters and optical cavities is essential for scalable quantum photonic technologies. Group-IV vacancy centers in diamond, particularly the negatively charged tin-vacancy center, have emerged as promising candidates due to their spectral stability, high Debye-Waller factor, and large orbital splitting in ground states. Here, we demonstrate controlled coupling of a single negatively charged tin-vacancy center hosted in a nanodiamond to a fully tunable Fabry-Pérot microcavity. At cryogenic temperatures, we access the weak-coupling regime and observe a transition from the bad-emitter regime to the bad-cavity regime as the optical transition of the color center narrows. At 4 K, a Purcell factor exceeding 1.7 is measured, confirming cavity-enhanced emission. The obtained results demonstrate the potential of Sn − V − centers in nanodiamonds as a coherent single-photon source for quantum networks.