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Nano Letters

Plasmonic Nanocavity-Assisted Long-Range Dipole–Dipole Interactions for Rare-Earth Ions

Xin Xie, Bowen Kang, Huatian Hu, Lei Guo, Mengya Zhang, Chengxiang Gou, Ke Kang, Wangze Li, Huan Chen, Zhenglong Zhang

Published Feb 5, 2026• 0 citations
Publisher

Abstract

) exhibit sharp 4f-4f transitions that are highly sensitive to dipole-dipole interactions (DDIs), yet the intrinsic short-range of DDIs restricts their application in long-distance quantum coupling. Here, we demonstrate a plasmonic nanocavity pair that simultaneously couples to upconversion nanoparticles (UCNPs) and quantum dots (QDs), enabling enhanced emission and inter-emitter interaction. The combined effects of Purcell enhancement and surface plasmon polariton (SPP) propagation extend the DDI-mediated energy transfer over a record distance exceeding 7.5 μm, 2 orders of magnitude longer than conventional Förster resonance systems. Moreover, the polarization-controlled SPP propagation directs the in-plane energy redistribution, achieving anisotropic and tunable coupling. This work establishes a viable route toward controllable, long-range DDIs among rare-earth emitters, advancing integrated quantum photonic architectures.

DOI
10.1021/acs.nanolett.5c05665

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) exhibit sharp 4f-4f transitions that are highly sensitive to dipole-dipole interactions (DDIs), yet the intrinsic short-range of DDIs restricts their application in long-distance quantum coupling. Here, we demonstrate a plasmonic nanocavity pair that simultaneously couples to upconversion nanoparticles (UCNPs) and quantum dots (QDs), enabling enhanced emission and inter-emitter interaction. The combined effects of Purcell enhancement and surface plasmon polariton (SPP) propagation extend the DDI-mediated energy transfer over a record distance exceeding 7.5 μm, 2 orders of magnitude longer than conventional Förster resonance systems. Moreover, the polarization-controlled SPP propagation directs the in-plane energy redistribution, achieving anisotropic and tunable coupling. This work establishes a viable route toward controllable, long-range DDIs among rare-earth emitters, advancing integrated quantum photonic architectures.
Long-range dipole-dipole interactions (DDIs) are essential for enabling scalable quantum technologies. However, their practical realization is fundamentally limited by spatial rapid decay and environmental noise. In this study, we propose a plasmon-assisted microcavities platform that integrates a photonic cavity with a plasmonic antenna for enhanced energy transfer between donors and acceptors. Benefiting from the resonating of the acceptors within the microcavity after receiving energy, stable long-range DDIs with an interaction distance of ∼13.6 μm and lasing emission can be achieved at ambient temperature. The results of this study suggest the potential for long-range, efficient DDIs in on-chip quantum systems with potential applications in quantum sensing and energy harvesting.
Quantum light-matter interfaces connecting stationary qubits to photons will enable optical networks for quantum communications, precise global time keeping, photon switching and studies of fundamental physics. Rare-earth-ion-doped crystals are state-of-the-art materials for optical quantum memories and quantum transducers between optical photons, microwave photons and spin waves. Here we demonstrate coupling of an ensemble of neodymium rare-earth-ions to photonic nanocavities fabricated in the yttrium orthosilicate host crystal. Cavity quantum electrodynamics effects including Purcell enhancement (F=42) and dipole-induced transparency are observed on the highly coherent (4)I(9/2)-(4)F(3/2) optical transition. Fluctuations in the cavity transmission due to statistical fine structure of the atomic density are measured, indicating operation at the quantum level. Coherent optical control of cavity-coupled rare-earth ions is performed via photon echoes. Long optical coherence times (T2∼100 μs) and small inhomogeneous broadening are measured for the cavity-coupled rare-earth ions, thus demonstrating their potential for on-chip scalable quantum light-matter interfaces.
Near-infrared (NIR) emitters operating in the 650-900 nm range are highly attractive for imaging and sensing in turbid media; however, cadmium-free InP-based quantum dots (QDs) often suffer from limited brightness due to nonradiative pathways and inefficient photon outcoupling. In particular, heterostructured InP QDs can exhibit band alignments that induce partial spatial separation of charge carriers, leading to reduced electron-hole wavefunction overlap. This modifies intrinsic recombination dynamics and enhances the sensitivity of their emission to the surrounding photonic environment. Here, we investigate silver toroidal plasmonic nanoantenna dimers (Ag TPNDs) through finite-difference-time-domain (FDTD) simulations as a geometry-tunable platform for enhancing NIR emission of heterostructured InP-based QDs. The coupled toroidal geometry supports strongly confined bonding modes that generate intense nanogap hotspots, while its resonance can be systematically tuned through the toroid aspect ratio. By spectrally aligning the antenna response with QD emission bands (675-845 nm), we achieve large Purcell enhancements together with high quantum efficiencies, demonstrating efficient conversion of enhanced decay rates into radiative emission. We further show that nanometer-scale variations in emitter-antenna separation strongly modulate the radiative rates and spectral response. These results establish toroidal plasmonic nanodimers as a topology-driven platform for controlling emission in NIR quantum emitters and for advancing NIR nanophotonic applications.
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.
In this review article, we discuss the many-body interactions in plasmonic nanohybrids made of an ensemble of quantum emitters and metallic nanoparticles. A theory of the linear and nonlinear optical emission intensity was developed by using the many-body quantum mechanical density matrix method. The ensemble of quantum emitters and metallic nanoparticles interact with each other via the dipole-dipole interaction. Surfaces plasmon polaritons are located near to the surface of the metallic nanoparticles. We showed that the nonlinear Kerr intensity enhances due to the weak dipole-dipole coupling limits. On the other hand, in the strong dipole-dipole coupling limit, the single peak in the Kerr intensity splits into two peaks. The splitting of the Kerr spectrum is due to the creation of dressed states in the plasmonic nanohybrids within the strong dipole-dipole interaction. Further, we found that the Kerr nonlinearity is also enhanced due to the interaction between the surface plasmon polaritons and excitons of the quantum emitters. Next, we predicted the spontaneous decay rates are enhanced due to the dipole-dipole coupling. The enhancement of the Kerr intensity due to the surface plasmon polaritons can be used to fabricate nanosensors. The splitting of one peak (ON) two peaks (OFF) can be used to fabricate the nanoswitches for nanotechnology and nanomedical applications.
Spontaneous emission from ensembles of quantum emitters (QEs) such as atoms, molecules or semiconductor quantum dots can be greatly enhanced by cooperative effects arising from electromagnetic correlations. We describe a cooperative mechanism for emission of light by an ensemble of QEs based upon cooperative energy transfer from QEs to localized surface plasmons in metal-dielectric structures followed by plasmon radiation at a rate that scales with the ensemble size. For large QE ensembles saturating the plasmon mode volume, we derive universal, i.e. independent of local field distribution, expression for cooperative Purcell factor that can by far exceed the field enhancement limits for individual QE in a hot spot. We also derive radiated power spectrum that retains the plasmon resonance lineshape and, in contrast to common cooperative mechanisms, is insensitive to natural variations of QEs' emission frequencies.