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arXiv:2312.14313 · PRX Quantum

Lifetime Reduction of Single Germanium-Vacancy Centers in Diamond via a Tunable Open Microcavity

Rigel Zifkin, César Daniel Rodríguez Rosenblueth, Erika Janitz, Yannik Fontana, Lilian Childress

Published Jul 15, 2024• 13 citations
arXivHTMLPDF

Abstract

Coupling between a single quantum emitter and an optical cavity presents a key capability for future quantum networking applications. Here, we explore interactions between individual germanium-vacancy ( Ge V) defects in diamond and an open microcavity at cryogenic temperatures. Exploiting the tunability of our microcavity system to characterize and select emitters, we observe a Purcell-effect-induced lifetime reduction of up to 4.5±0.3 and extract coherent-coupling rates up to 360±20 MHz. Our results indicate that the Ge V defect has favorable optical properties for cavity coupling, with a quantum efficiency of at least 0.34±0.05 and likely much higher. Published by the American Physical Society 2024

DOI
10.1103/prxquantum.5.030308

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Quantum Photonic Devices•Sep 19, 2017•4 citations
Coupling between a single quantum emitter and an optical cavity presents a key capability for future quantum networking applications. Here, we explore interactions between individual germanium-vacancy ( Ge V) defects in diamond and an open microcavity at cryogenic temperatures. Exploiting the tunability of our microcavity system to characterize and select emitters, we observe a Purcell-effect-induced lifetime reduction of up to 4.5±0.3 and extract coherent-coupling rates up to 360±20 MHz. Our results indicate that the Ge V defect has favorable optical properties for cavity coupling, with a quantum efficiency of at least 0.34±0.05 and likely much higher. Published by the American Physical Society 2024
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Solid-state quantum emitters such as the N-VVV center in diamond have applications ranging from single-photon sources to quantum sensors, with some quantum properties preserved even under ambient conditions. A central challenge is to access these quantum properties efficiently, by catching as much emitted light as possible. In this study a tunable optical microcavity, with a mode volume as small as one wavelength cubed, is used to enhance spontaneous emission of single N-VVV centers in diamond, via the Purcell effect. This allows the authors to extract large amounts of light from several individually addressable emitters, and to control their spontaneous-emission rate.
The Nitrogen-Vacancy (NV) centre in diamond possesses an optical read out of its spin state and shows great promise for applications in solid state quantum technologies. Its broad phonon assisted emission spectrum, with only 4% of emission from the zero-phonon line, is a major drawback to this. The optical microcavity will be essential in efficiently interfacing these centres with photonic networks. Here we present investigations into the coupling of NV centres in nanodiamond to tunable open-microcavities, both at room temperature and at cryogenic temperatures. These structures will be shown to achieve good photon confinement, with mode volumes down to 5λ3. Room temperature studies on ensembles of NVs will illustrate the tunable spectral and spatial overlap between the emitter and the cavity mode. It will be shown that small enhancements are possible in this regime. After the preparation and characterisation of single emitters, low temperature coupling to the narrowed zero-phonon line will be the central theme of this thesis. Single photon emission into the cavity mode is verified. We observe the enhancement of the light-matter interaction in this regime, by a 39% increase in the emission rate when cavity-coupled, with the dependence on mode volume also demonstrated. These results are important for the realisation of a spin-photon interface in scalable quantum networks.
Recent demonstrations of entanglement between two remote Nitrogen-Vacancy centers, have opened the way for their use in distributed quantum networks. An efficient spin-photon interface will now be required to help realize this system as a technology. Here we demonstrate the tunable enhancement of the zero phonon line of a single nitrogen-vacancy colour centre in nanodiamond at cryogenic temperatures. A plano-hemispherical open cavity, fabricated using focused ion beam milling provides mode volumes as small as 1.25 cubic microns and quality factor Q ~ 3000. It will be shown how the open geometry and independently adjustable mirrors allows for precise placement of the emitter in the centre of the cavity mode, and crucially enables in-situ tuning of the cavity resonances. At optimal coupling, the signal from individual zero phonon line transitions is enhanced by a factor of 6.25 through the Purcell effect and the overall emission rate of the NV- centre is increased by 40% compared with that measured from the same centre in the absence of cavity field confinement. This Purcell enhancement is mapped out as a function of cavity mode volume. These results represent a proof of principle for a tunable cryogenic spin-photon interface. However by far the best NV optical and spin coherences are to be found in bulk material and efforts towards the production of diamond membranes are currently being made, with dimensions suitable for open-cavity coupling. Efforts towards this and preliminary results will also be discussed.
The Nitrogen-Vacancy (NV) centre in diamond possesses an optical read out of its spin state and shows great promise for applications in solid state quantum technologies. Its broad phonon assisted emission spectrum, with only 4p of emission from the zero-phonon line, is a major drawback to this. The optical microcavity will be essential in efficiently interfacing these centres with photonic networks. Here we present investigations into the coupling of NV centres in nanodiamond to tunable open-microcavities, both at room temperature and at cryogenic temperatures. These structures will be shown to achieve good photon confinement, with mode volumes down to 5λ3. Room temperature studies on ensembles of NVs will illustrate the tunable spectral and spatial overlap between the emitter and the cavity mode. It will be shown that small enhancements are possible in this regime. After the preparation and characterisation of single emitters, low temperature coupling to the narrowed zero-phonon line will be the central theme of this thesis. Single photon emission into the cavity mode is verified. We observe the enhancement of the light-matter interaction in this regime, by a 39p increase in the emission rate when cavity-coupled, with the dependence on mode volume also demonstrated. These results are important for the realisation of a spin-photon interface in scalable quantum networks.
A key requirement for many applications in solid-state quantum sciences is a high fluence of indistinguishable photons. The spontaneous emission of these photons is governed by the coupling of an excited quantum system to electromagnetic vacuum fluctuations. In our experiment, we enhance this coupling by engineering a tunable Fabry-Perot microcavity. The quantum system we study is the nitrogen-vacancy (NV) center in diamond, a workhorse for quantum science and engineering, due to its optical transitions and the coherent electron spin system it hosts. Our device consists of a high-quality, nano-fabricated, single-crystalline diamond membrane bonded to a planar mirror; the cavity is completed by a second, concave mirror. Using piezo positioners, we achieve full spectral and spatial tunability and freedom in selecting NVs with favorable emission properties in our low-temperature (4 Kelvin) experiments. Upon tuning of the cavity into resonance, we find significant enhancement of the 637 nm zero phonon line for several individual NVs which is accompanied by a strong reduction of the overall photoluminescence (PL) lifetime. We infer a 30-fold enhancement of the zero-phonon transition rate at best. The fraction of the PL emission associated to this resonant transition is thereby increased from 3% to 46%. Our results constitute a significant leap on the route towards the implementation of fast long-distance quantum networks, which are currently limited by the photon emission rate in their nodes. Furthermore, our versatile design is readily applicable to other solid-state quantum emitters like color centers in silicon carbide.