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arXiv:2512.02907

Tunable giant Purcell enhancement of quantum light emitters by means of acoustic graphene plasmons

Justin Gruber, Mahtab A. Khan, Dirk R. Englund, Michael N. Leuenberger

cond-mat.mes-hallquant-phSubmitted Dec 2, 2025• Announced Dec 3, 2025
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Abstract

Inspired by the remarkable ability of plasmons to boost radiative emission rates, we propose leveraging acoustic graphene plasmons (AGPs) to realize tunable, giant Purcell enhancements for single-photon, entangled-photon, and multipolar quantum emitters. These AGPs are localized inside a cavity defined by a graphene sheet and a metallic nanocube and filled with a dielectric of thickness of a few nanometers and consisting of stacked layers of 2D materials, containing impurities or defects that act as quantum light emitters. Through finite-difference time domain (FDTD) calculations, we show that this geometry can achieve giant Purcell enhancement factors over a large portion of the infrared (IR) spectrum, up to 6 orders of magnitude in the mid-IR and up to 4 orders of magnitude at telecommunications wavelengths, reaching quantum efficiencies of 95\% and 89\%, respectively, with high-mobility graphene. We obtain Purcell enhancement factors for single-photon electric dipole (E1), electric quadrupole (E2), and electric octupole (E3) transitions and two-photon spontaneous emission (2PSE) transitions, of the orders of $10^{4}$, $10^{7}$, $10^{9}$, and $10^9$, respectively, and a quantum efficiency of 79\% for entangled-photon emission with high-mobility graphene at a wavelength of $λ=1.55$ $μ$m. Importantly, AGP mode frequencies depend on the graphene Fermi energy, which can be tuned via electrostatic gating to modulate fluorescence enhancement in real time. As an example, we consider the Purcell enhancement of spontaneous single- and two-photon emissions from an erbium atom inside single-layer (SL) WS$_2$. Our results could be useful for electrically tunable quantum emitter devices with applications in quantum communication and quantum information processing.

Comments
18 pages, 10 figures

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The enhancement of two-photon spontaneous emission (2PSE) from trivalent and divalent rare earth ions in proximity to graphene and graphene nanoribbons is calculated for achievable experimental conditions using a combination of finite difference time domain simulations and direct computation of transition rates between energy levels in rare earths. For Er3+{\mathrm{Er}}^{3+}Er3+, we find that the 2PSE rate is initially 8 orders lower than the single-photon spontaneous emission rate but that, with enhancement, 2PSE can reach 2.5% of the overall decay. When graphene nanoribbons are used, we also show that the emission of free-space photon pairs from Er3+{\mathrm{Er}}^{3+}Er3+ at 3--3.2 $\ensuremath{\mu}\mathrm{m}$ via 2PSE can be increased by $\ensuremath{\sim}400$. Our calculations show significantly less relative graphene-enhanced 2PSE than previous works, and we attribute this variation to differences in emitter size and assumed graphene mobility. We also show that the internal energy structure of the ion can have an impact on the degree of 2PSE enhancement achievable and find that divalent rare earths are more favorable.
Combining the quantum optical properties of single-photon emitters with the strong near-field interactions available in nanophotonic and plasmonic systems is a powerful way of creating quantum manipulation and metrological functionalities. The ability to actively and dynamically modulate emitter-environment interactions is of particular interest in this regard. While thermal, mechanical and optical modulation have been demonstrated, electrical modulation has remained an outstanding challenge. Here we realize fast, all-electrical modulation of the near-field interactions between a nanolayer of erbium emitters and graphene, by in-situ tuning the Fermi energy of graphene. We demonstrate strong interactions with a >1000-fold increased decay rate for ~25% of the emitters, and electrically modulate these interactions with frequencies up to 300 kHz - orders of magnitude faster than the emitter's radiative decay (~100 Hz). This constitutes an enabling platform for integrated quantum technologies, opening routes to quantum entanglement generation by collective plasmon emission or photon emission with controlled waveform.
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.
Abstract 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.
The rate of spontaneous emission is known to depend on the environment of a emitter, and the enhancement of one-photon emission in a resonant cavity is known as the Purcell effect. Here we develop a theory of spontaneous two-photon emission for a general electromagnetic environment including inhomogeneous dispersive and absorptive media. This theory is used to evaluate the two-photon Purcell enhancement in the vicinity of metallic nanoparticles and demonstrates that the surface-plasmon resonances supported by these particles can increase the emission rate by more than two orders of magnitude. The control over two-photon Purcell enhancement given by tailored nanostructured environments could provide an emitter with any desired spectral response and may serve as an ultimate route for designing light sources with novel properties.
Single-photon sources that are bright, pure, and interference-ready are essential for quantum communication and photonic quantum information processing, but many solid-state platforms still rely on bulky optical excitation, careful alignment, and post-selection to achieve useful linewidth, stability, and brightness. Scalable quantum photonics instead requires turnkey quantum-light engines that can be triggered on demand, stabilized against environmental noise, and efficiently interfaced with fibers or photonic circuits. This review surveys recent progress in electronic and photonic integration of single quantum emitters in two-dimensional materials, focusing on localized excitonic emitters in transition metal dichalcogenides and defect-based color centers in hexagonal boron nitride. On the electronic side, we discuss electrical injection, fast modulation, electrostatic stabilization, and Stark tunability as routes to suppress blinking, spectral wandering, and charge-noise-induced broadening. On the photonic side, we review waveguide and resonator platforms that funnel emission into well-defined optical modes and, in some cases, enhance radiative rates through the Purcell effect. We connect these integration strategies to key source metrics, including single-photon purity, brightness, spectral stability, and photon indistinguishability. We conclude that the next stage of progress will depend on co-designed electronic and photonic architectures that jointly optimize on-demand operation, stabilization, tunability, and packaging-compatible optical interfacing.