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Quantum 2.0 Conference and Exhibition

A quantum network node based on SnV centers in diamond

David Hunger, Jeremias Resch, Ioannis Karapatzakis, Kerim Köster, Andras Lauko, Marcel Schrodin, Philipp Fuchs, Michael Kieschnick, Julia Heupel, Cyril Popov, Jan Meijer, Christoph Becher, Wolfgang Wernsdorfer

Published Jan 1, 2025• 0 citations
Publisher

Abstract

We report spin control of a tin vacancy center in diamond and observe a coherence time of up to 10 ms. We also control a nearby carbon nuclear spin with up to 1 s coherence. Finally, we incorporate SnV centers in a microcavity and achieve a cooperativity of 0.3, substantiating the potential of SnV centers in diamond for quantum network nodes.

DOI
10.1364/quantum.2025.qm3a.7

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arXiv:2106.00723•Physical Review X•Nov 30, 2021•84 citations
We report spin control of a tin vacancy center in diamond and observe a coherence time of up to 10 ms. We also control a nearby carbon nuclear spin with up to 1 s coherence. Finally, we incorporate SnV centers in a microcavity and achieve a cooperativity of 0.3, substantiating the potential of SnV centers in diamond for quantum network nodes.
Quantum emitters in diamond are a promising candidate for quantum network applications. Here, we show basic properties of tin-vacancy (SnV) centers in diamond, which we recently discovered. The SnV center shows a sharp zero phonon line and a high fluorescence intensity. The SnV center has a possibility to have a long spin coherence time in the Kelvin temperature range, in contrast to other group-IV color centers, i.e. silicon-vacancy and germanium-vacancy centers. We discuss important experiments regarding spin and optical properties of the SnV quantum emitter for further development towards quantum network.
Solid-state quantum emitters that couple coherent optical transitions to long-lived spin qubits are essential for quantum networks. Here we report on the spin and optical properties of individual tin-vacancy (SnV) centers in diamond nanostructures. Through cryogenic magneto-optical and spin spectroscopy, we verify the inversion-symmetric electronic structure of the SnV, identify spin-conserving and spin-flipping transitions, characterize transition linewidths, measure electron spin lifetimes, and evaluate the spin dephasing time. We find that the optical transitions are consistent with the radiative lifetime limit even in nanofabricated structures. The spin lifetime is phonon limited with an exponential temperature scaling leading to T_{1}>10 ms, and the coherence time, T_{2}^{*} reaches the nuclear spin-bath limit upon cooling to 2.9 K. These spin properties exceed those of other inversion-symmetric color centers for which similar values require millikelvin temperatures. With a combination of coherent optical transitions and long spin coherence without dilution refrigeration, the SnV is a promising candidate for feasable and scalable quantum networking applications.
The realization of quantum networks critically depends on establishing efficient, coherent light-matter interfaces. Optically active spins in diamond have emerged as promising quantum nodes based on their spin-selective optical transitions, long-lived spin ground states, and potential for integration with nanophotonics. Tin-vacancy (SnV -^{\,\textrm{-}}-) centers in diamond are of particular interest because they exhibit narrow-linewidth emission in nanostructures and possess long spin coherence times at temperatures above 1 K. However, a nanophotonic interface for SnV -^{\,\textrm{-}}- centers has not yet been realized. Here, we report cavity enhancement of the emission of SnV -^{\,\textrm{-}}- centers in diamond. We integrate SnV -^{\,\textrm{-}}- centers into one-dimensional photonic crystal resonators and observe a 40-fold increase in emission intensity. The Purcell factor of the coupled system is 25, resulting in channeling of the majority of photons (90%90\%90%) into the cavity mode. Our results pave the way for the creation of efficient, scalable spin-photon interfaces based on SnV -^{\,\textrm{-}}- centers in diamond.
Group-IV color centers in diamond are a promising light-matter interface for quantum networking devices.The negatively charged tin-vacancy center (SnV) is particularly interesting, as its large spin-orbit coupling offers strong protection against phonon dephasing and robust cyclicity of its optical transitions toward spin-photon-entanglement schemes.Here, we demonstrate multiaxis coherent control of the SnV spin qubit via an all-optical stimulated Raman drive between the ground and excited states.We use coherent population trapping and optically driven electronic spin resonance to confirm coherent access to the qubit at 1.7 K and obtain spin Rabi oscillations at a rate of Ω=2π ¼ 19.0ð1Þ MHz.All-optical Ramsey interferometry reveals a spin dephasing time of T Ã 2 ¼ 1.3ð3Þ μs, and four-pulse dynamical decoupling already extends the spin-coherence time to T 2 ¼ 0.30ð8Þ ms.Combined with transform-limited photons and integration into photonic nanostructures, our results make the SnV a competitive spin-photon building block for quantum networks.