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SPIE Nanophotonics

Cavity-enhanced organic single-photon emitters

Margarita Anna Zommere, Maja Colautti, Elena Fanella, Rocco Duquennoy, Sven Burger, Fridtjof Betz, Elisabetta Rosadoni, Andrea Ottomaniello, Virgilio Mattoli, Costanza Toninelli

Published Apr 10, 2026• 0 citations
Publisher
DOI
10.1117/12.3099825

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Single organic molecules are a well-established platform for high-quality single-photon generation: they can emit lifetime-limited photons with high purity and indistinguishability. However, their emission is accompanied by a pronounced red-shifted phonon sideband and higher-order vibrational peaks, which reduce the fraction of photons emitted into the desired narrowband zero-phonon line. The standard approach to suppressing this unwanted emission is to integrate the emitter into a monolithic photonic nanostructure that provides Purcell enhancement. However, incorporating organic materials using clean-room techniques has proven challenging, and has in fact so far prevented their integration into monolithic microcavities altogether. As a result, efficient, narrowband organic single-photon sources for applications in quantum information processing have remained elusive despite their considerable promise. Here, we propose three monolithic microcavity designs tailored to provide sufficient Purcell enhancement for organic quantum emitters. The Purcell effect induced by these cavities preferentially enhances emission into the 0-0 zero-phonon line, increasing spectral purity, photon extraction, and shortening the excited-state lifetime, which in turn relaxes the requirements for generating indistinguishable photons. The cavities have been optimized using Bayesian optimization and the adaptive Antoulas-Anderson (AAA) algorithm for rational approximation, which offer global optimization and the efficient reconstruction of spectra from scattering simulations, respectively. These structures are compatible with both standard clean-room processing and single-molecule preparation techniques. Therefore, they offer a clear route to realize high-quality, practically monochromatic organic single-photon light sources.
Single-photon emitters (SPEs) based on nitrogen-vacancy centers in nanodiamonds (neutral NV0 (wavelength 575 nm) and negative NV- (wavelength 637 nm)) represent promising platforms for quantum nanophotonics applications, yet their emission efficiencies remain constrained by weak light-matter interactions. Multi-layer metasurfaces (MLM) offer unprecedented degrees of freedom for efficient light manipulation beyond conventional single-material metasurfaces, enabling dual-resonance cavities that can simultaneously enhance pump excitation and SPE collection. However, traditional trial-and-error and forward optimization methods face significant challenges in designing these complex structures due to the vast parameter space and computational demands. Here, we present NanoPhotoNet-Inverse, an artificial intelligence-driven inverse design framework based on a hybrid deep neural network architecture. This model efficiently performs inverse design of two dual-resonance MLM cavities to amplify pump and SPE emissions of different vacancies in nanodiamond and improve SPE collection. Our approach achieves inverse design prediction efficiency exceeding 98.7%, demonstrating three orders of magnitude amplification in SPE count rate and 50 picosecond lifetime, significantly surpassing conventional cavity designs. These remarkable enhancements in emission rates and collection efficiency position our platform as a transformative technology for advancing quantum communication networks, quantum computing architectures, quantum sensing applications, and quantum cryptography systems. Therefore, it opens new pathways for intelligent photonic device engineering in quantum technologies.
Atom-like defects in hexagonal boron nitride (hBN) provide room-temperature single-photon emission and coherent spin states, making them attractive for quantum-computing and -sensing applications. However, their random spatial and spectral characteristics hamper deterministic coupling with nano-optical cavities, limiting their use as bright single-photon sources and sensitive quantum sensors. Here, we present tip-enhanced quantum-sensing spectroscopy of single-photon emitters in hBN. Through precise spatial positioning of individual emitters within tip-cavities with different plasmon resonances, we adaptively control the enhancement rates of both excitation and emission, as well as the single-photon purity. In this way, optimal selection of their relative contributions can effectively reconfigure solid-state single-photon sources, with simultaneous nano-spectroscopic space- and time-resolved analyses. Furthermore, we demonstrate tip-enhanced quantum-sensing with single spin defects through optically detected magnetic resonance (ODMR) experiments in tip-coupled hBN nanoflakes. Our approach provides a unique pathway toward highly-sensitive and deterministic quantum-sensing with room-temperature single-photon emitters.