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Conference on Lasers and Electro-Optics

Fluorescence enhancement of Er3+-ions using reverse hybrid plasmonic nano-focusing

Nicholas A. Güsken, Ming Fu, Maximilian Zapf, Michael P. Nielsen, Paul M. Dichtl, Robert Röder, Stefan Alexander Maier, Carsten Ronning, Mark L. Brongersma, Rupert F. Oulton

Published Jan 1, 2022• 0 citations
Publisher

Abstract

We report the broadband fluorescence enhancement of erbium ions embedded in a single non-resonant reverse nano-focusing waveguide. We measure a large radiative Purcell enhancement of a total emission rate enhancement of > 250 across the entire measured spectrum including the prominent telecoms C-band. Further, we observe the enhancement of single electric dipole transitions from Stark-split levels at room temperature.

DOI
10.1364/cleo_qels.2022.ff3c.4

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We report the broadband fluorescence enhancement of erbium ions embedded in a single non-resonant reverse nano-focusing waveguide. We measure a large radiative Purcell enhancement of a total emission rate enhancement of > 250 across the entire measured spectrum including the prominent telecoms C-band. Further, we observe the enhancement of single electric dipole transitions from Stark-split levels at room temperature.
We report the broadband luminescence enhancement of erbium ions embedded in a non-resonant hybrid waveguide photon-emitter interface on silicon. The measured emission rate enhancement of > 300 is enabled by a large radiative Purcell factor across the spectrum in the telecommunications C-band. This enables the shortening of the lifetime of erbium from 3 ms to 8 μs, effectively providing brighter on-chip photon sources. The platform efficiently collects the photon emission of erbium in a single-mode waveguide and out-couples it to a low-loss photonic waveguide using a reverse nano-focusing method. This hybrid approach opens a large range of possible emitter-waveguide platform combinations for heterogeneous and hybrid quantum emitter integration, towards scalable on-chip quantum networks.
Abstract Since Purcell’s seminal report 75 years ago, electromagnetic resonators have been used to control light-matter interactions to make brighter radiation sources and unleash unprecedented control over quantum states of light and matter. Indeed, optical resonators such as microcavities and plasmonic antennas offer excellent control but only over a limited spectral range. Strategies to mutually tune and match emission and resonator frequency are often required, which is intricate and precludes the possibility of enhancing multiple transitions simultaneously. In this letter, we report a strong radiative emission rate enhancement of Er 3+ -ions across the telecommunications C-band in a single plasmonic waveguide based on the Purcell effect. Our gap waveguide uses a reverse nanofocusing approach to efficiently enhance, extract and guide emission from the nanoscale to a photonic waveguide while keeping plasmonic losses at a minimum. Remarkably, the large and broadband Purcell enhancement allows us to resolve Stark-split electric dipole transitions, which are typically only observed under cryogenic conditions. Simultaneous radiative emission enhancement of multiple quantum states is of great interest for photonic quantum networks and on-chip data communications.
Single quantum emitters embedded in solid-state hosts are an ideal platform for realizing quantum information processors and quantum network nodes. Among the currently investigated candidates, Er^{3+} ions are particularly appealing due to their 1.5 μm optical transition in the telecom band as well as their long spin coherence times. However, the long lifetimes of the excited state-generally in excess of 1 ms-along with the inhomogeneous broadening of the optical transition result in significant challenges. Photon emission rates are prohibitively small, and different emitters generally create photons with distinct spectra, thereby preventing multiphoton interference-a requirement for building large-scale, multinode quantum networks. Here we solve this challenge by demonstrating for the first time linear Stark tuning of the emission frequency of a single Er^{3+} ion. Our ions are embedded in a lithium niobate crystal and couple evanescently to a silicon nanophotonic crystal cavity that provides a strong increase of the measured decay rate. By applying an electric field along the crystal c axis, we achieve a Stark tuning greater than the ion's linewidth without changing the single-photon emission statistics of the ion. These results are a key step towards rare earth ion-based quantum networks.
Erbium-doped solid-state crystals present an attractive platform for quantum communication, combining the telecom C-band spin–photon interface and long coherence times of erbium (Er3+) with the versatility of solid-state hosts. However, across commonly investigated materials, Er3+ is a “dim” ion, with low optical emission rates of kilohertz at most. This makes implementing quantum information transfer protocols (e.g., quantum teleportation) at usable rates a major challenge. One route to increasing Er3+ radiative rates is by careful selection of crystal hosts: the crystal field around an Er3+ ion may hybridize states of different parity, potentially increasing the radiative rate of its telecom transition. Here, using high-throughput computational methods, the radiative rates of Er3+ embedded in 9215 materials are estimated. The computation shows that careful host selection could increase Er3+ radiative rates by an order of magnitude compared to commonly studied hosts. Calculated results are compared with experimental radiative rates in a subset of materials, finding notable clustering but weak correlation. Nevertheless, the “brightest” candidates combined with suitable nanophotonics engineering could push Er3+-based quantum memories into the megahertz bandwidth regime.
Single quantum emitters coupled to optical cavities in the Purcell regime can be used as high-efficiency spin-photon interfaces that are essential for building a quantum network. Furthermore, the dynamical control of the spontaneous emission rate of quantum emitters can have important implications in quantum technologies, e.g. for shaping the emitted photons waveform, or for driving coherently the optical transition while preventing photon emission. Here we demonstrate the dynamical Purcell-enhanced emission of a mesoscopic ensemble of erbium ions doped into nanocrystals coupled to a fully-tunable high-finesse fiber-based optical microcavity. Erbium has excellent optical and spin coherence properties at cryogenic temperatures and, in addition, has a transition in the telecom band that can facilitate integration into existing commercial telecom fibers. We show that we can tune the cavity on and out of resonance at a rate of above 8 KHz, which is two orders of magnitude faster that the natural lifetime of the erbium ions (55 Hz), and a factor of five faster than the Purcell enhanced emission (1.8 KHz). This allows us to shape in real time the Purcell enhanced emission of the ions and to achieve full control over the emitted photon’s waveforms. With moderate improvements in our detection efficiency and cavity finesse, this capability will allow for the generation of single telecom photons with controllable wave-shape from single erbium ions and for the realization of quantum processing between rare-earth ion qubits using dipolar interactions.
The interaction of single quantum emitters with an optical cavity enables the realization of efficient spin-photon interfaces, an essential resource for quantum networks. The dynamical control of the spontaneous emission rate of quantum emitters in cavities has important implications in quantum technologies, e.g., for shaping the emitted photons' waveform or for driving coherently the optical transition while preventing photon emission. Here we demonstrate the dynamical control of the Purcell enhanced emission of a small ensemble of erbium ions doped into a nanoparticle. By embedding the nanoparticles into a fully tunable high finesse fiber based optical microcavity, we demonstrate a median Purcell factor of 15 for the ensemble of ions. We also show that we can dynamically control the Purcell enhanced emission by tuning the cavity on and out of resonance, by controlling its length with sub-nanometer precision on a time scale more than two orders of magnitude faster than the natural lifetime of the erbium ions. This capability opens prospects for the realization of efficient nanoscale quantum interfaces between solid-state spins and single telecom photons with controllable waveform, for non-destructive detection of photonic qubits, and for the realization of quantum gates between rare-earth ion qubits coupled to an optical cavity.