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arXiv:1910.03005 · Advanced Optical Materials

Chip‐Compatible Quantum Plasmonic Launcher

Chin‐Cheng Chiang, Simeon Bogdanov, Oksana Makarova, Xiaohui Xu, Soham Saha, Deesha Shah, Zachariah O. Martin, Di Wang, Alexei Lagutchev, Alexander V. Kildishev, Alexandra E. Boltasseva, Vladimir M. Shalaev

Published Aug 2, 2020• 14 citations
arXivHTMLPDF

Abstract

Abstract Integrated on‐demand single‐photon sources are critical for the implementation of photonic quantum information processing systems. To enable practical quantum photonic devices, the emission rates of solid‐state quantum emitters need to be substantially enhanced and the emitted signal must be directly coupled to an on‐chip circuitry. The photon emission rate speed‐up is best achieved via coupling to plasmonic antennas, while on‐chip integration can be realized by directly coupling emitters to photonic waveguides. The realization of practical devices requires that both the emission speed‐up and efficient out‐coupling are achieved in a single architecture. Here, a novel architecture is proposed that combines chip compatibility with high radiative emission rates—a quantum plasmonic launcher. The proposed launchers contain single nitrogen‐vacancy (NV) centers in nanodiamonds as quantum emitters that offer record‐high average fluorescence lifetime shortening factors of about 7000 times. Nanodiamonds with single NVs are sandwiched between two silver films that couple more than half of the emission into in‐plane propagating surface plasmon polaritons. This simple, compact, and scalable architecture represents a crucial step toward the practical realization of high‐speed on‐chip quantum networks.

DOI
10.1002/adom.202000889

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Abstract Integrated on‐demand single‐photon sources are critical for the implementation of photonic quantum information processing systems. To enable practical quantum photonic devices, the emission rates of solid‐state quantum emitters need to be substantially enhanced and the emitted signal must be directly coupled to an on‐chip circuitry. The photon emission rate speed‐up is best achieved via coupling to plasmonic antennas, while on‐chip integration can be realized by directly coupling emitters to photonic waveguides. The realization of practical devices requires that both the emission speed‐up and efficient out‐coupling are achieved in a single architecture. Here, a novel architecture is proposed that combines chip compatibility with high radiative emission rates—a quantum plasmonic launcher. The proposed launchers contain single nitrogen‐vacancy (NV) centers in nanodiamonds as quantum emitters that offer record‐high average fluorescence lifetime shortening factors of about 7000 times. Nanodiamonds with single NVs are sandwiched between two silver films that couple more than half of the emission into in‐plane propagating surface plasmon polaritons. This simple, compact, and scalable architecture represents a crucial step toward the practical realization of high‐speed on‐chip quantum networks.
Solid-state quantum emitters are in high demand for emerging technologies such as advanced sensing and quantum information processing. Generally, these emitters are not sufficiently bright for practical applications, and a promising solution consists in coupling them to plasmonic nanostructures. Plasmonic nanostructures support broadband modes, making it possible to speed up the fluorescence emission in room-temperature emitters by several orders of magnitude. However, one has not yet achieved such a fluorescence lifetime shortening without a substantial loss in emission efficiency, largely because of strong absorption in metals and emitter bleaching. Here, we demonstrate ultrabright single-photon emission from photostable nitrogen-vacancy (NV) centers in nanodiamonds coupled to plasmonic nanocavities made of low-loss single-crystalline silver. We observe a 70-fold difference between the average fluorescence lifetimes and a 90-fold increase in the average detected saturated intensity. The nanocavity-coupled NVs produce up to 35 million photon counts per second, several times more than the previously reported rates from room-temperature quantum emitters.
Ultrafast emission rates obtained from quantum emitters coupled to plasmonic nanoantennas have recently opened fundamentally new possibilities in quantum information and sensing applications. Plasmonic nanoantennas greatly improve the brightness of quantum emitters by dramatically shortening their fluorescence lifetimes. Gap plasmonic nanocavities that support strongly confined modes are of particular interest for such applications. We demonstrate single-photon emission from nitrogen-vacancy (NV) centers in nanodiamonds coupled to nanosized gap plasmonic cavities with internal mode volumes about 10 000 times smaller than the cubic vacuum wavelength. The resulting structures features sub-nanosecond NV excited-state lifetimes and detected photon rates up to 50 million counts per second. Analysis of the fluorescence saturation allows the extraction of the multi-order excitation rate enhancement provided by the nanoantenna. Efficiency analysis shows that the NV center is producing up to 0.25 billion photons per second in the far-field.
Single-photon sources are essential for quantum technologies, supporting secure communication, quantum computing, and integrated photonic systems. Nitrogen-vacancy (NV) centers in nanodiamonds are robust emitters that operate at room temperature and can be positioned on-chip, but efficient coupling to photonic modes remains challenging. We present the design, fabrication, and experimental characterization of a silicon nitride photonic structure engineered to enhance and extract emission from NV centers. The device features a subwavelength gap between waveguides, a Bragg reflector for emission redirection, and an output waveguide for collection. Simulations guided the optimization of the geometry to increase the spontaneous emission rate through photonic confinement. Nanodiamonds were deposited into the gap using lithographic patterning and drop-casting. Fluorescence lifetime measurements confirm that the structure modifies the emission dynamics of the NV centers. The approach is compatible with scalable fabrication techniques and offers a practical route toward integrated, chip-based single-photon sources.
Abstract Striving for nanometer‐sized solid‐state single‐photon sources, we investigate atom‐like quantum emitters based on single germanium‐vacancy (GeV) centers isolated in crystalline nanodiamonds (NDs). Cryogenic characterization indicated symmetry‐protected and bright (>10 6 counts/s with off‐resonance excitation) zero‐phonon optical transitions with up to 6‐fold enhancement in energy splitting of their ground states as compared to that found for GeV centers in bulk diamonds (i.e. up to 870 GHz in highly strained NDs vs. 150 GHz in bulk). Utilizing lithographic alignment techniques, we demonstrate an integrated nanophotonic platform for deterministic interfacing plasmonic waveguides with isolated GeV centers in NDs, which enables 10‐fold enhancement of single‐photon decay rates along with the emission direction control by judiciously designing and positioning a Bragg reflector. This approach allows one to realize the unidirectional emission from single‐photon dipolar sources, thereby opening new perspectives for the realization of quantum optical integrated circuits.
Very recently, the interest for quantum technologies by the scientific community and industry has strongly increased. Different types of implementations have been proposed as a practical implementation for a quantum bit. In particular, quantum photonics is a strong candidate for such applications. We are interested in using single photons and single spins in diamond as a solid state host matrix (nanodiamonds or membranes). Integration of nanosources of light is currently a major bottleneck preventing the realisation of all-photonic chips for quantum technologies and nanophotonics applications. Ideally, one needs optical circuitry, on-chip photodetection and on-chip generation of quantum states of light (single photons, entangled photons…). Our recent work on a new platform for quantum photonics using integrated optics can offer an easier and robust way to create compact quantum circuits that can be on chip and scalable. In this context, the coupling between waveguides and single photon emitters is critical. The goal of our research is to efficiently couple single photon emitters with a new platform made of optical glass waveguides. These waveguides are based on the so-called ion-exchange glass technology and is know in the photonics industry for quite some time but has never been used in the context of quantum technologies. Efficient light-matter interface is of primordial importance in this system. To achieve this goal, several paths are undertaken such as the use of dielectric and plasmonic structuration in order to increase the light interaction with the waveguide or to develop fabrication techniques to insert the emitters directly inside the guide (for nanodiamonds). We will show what is our current state of the art for placing single emitters at the right place on our optical waveguides made of ion-exchange in glass and in particular what can be done to improve our first promising results in order to get near unity coupling between the optical bus and single photon emitters. We will show first results with semiconductor nanocrystals (NCs) but also using nitrogen-vacancy and silicon-vacancy defects in nanodiamond. The very first step in of our approach consists in the design of the structured waveguide using electromagnetic FDTD. We demonstrated that it is possible to achieve more than 90% coupling. In practice, before using coloured centres in diamond, we started working with CdSe/ZnS semiconductor nanocrystals. So far, we use straight waveguides defined to be single modes at the nominal wavelength of the emission line of the nanoemitters. The positioning of nanoemitters is still a challenge to be achieved. We developed an original technique based on photopolymerisation of light where the nanocrystals are grafted into a light sensitive polymer and can be placed at adequate positions.
Very recently, the interest for quantum technologies by the scientific community and industry has strongly increased. Different types of implementations have been proposed as a practical implementation for a quantum bit as trapped atoms, superconducting qubits and single photons. In particular, we are interested in using single photons and single spins in solid state host matrices such as diamond (nanodiamonds or membranes). Integration of nanosources of light is currently a major bottleneck preventing the realisation of all-photonic chips for quantum technologies and nanophotonics applications. Nanophotonics and integrated optics are vast growing fields with huge market potentials in particular for quantum technologies. Ideally, one needs optical circuitry, on-chip photodetection and on-chip generation of quantum states of light (single photons, entangled photons…). We want to present our recent work on using integrated optics that can offer an easier and robust way to create fixed and compact quantum circuits that can be on chip and scalable. In this context, the coupling between waveguides and single photon emitters is critical. The goal of our research is to efficiently couple single photon emitters with a new platform made of optical glass waveguides. To achieve this goal, several paths are undertaken such as the use of dielectric and plasmonic structuration in order to increase the light interaction with the waveguide or to develop fabrication techniques to insert the emitters directly inside the guide (for nanodiamonds). We will show what is our current state of the art for placing single emitters at the right place on our optical waveguides made of ion-exchange in glass and in particular what can be done to improve our first promising results in order to get near unity coupling between the optical bus and single photon emitters. We will show first results with semiconductor nanocrystals (NCs) but also using nitrogen-vacancy defects in diamond either under nanodiamond form or in thin membranes.