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Demonstrates the growth of molecular emitter crystals for integrated photonics, suggesting improved optical coherence and device integration.
Organic molecules embedded in an organic matrix exhibit lifetime-limited optical coherence and bright emission at cryogenic temperatures below 3 K. Here, we present a simple vapor-phase growth method for synthesizing optically thin DBT-doped anthracene crystals that are compatible with integrated nanophotonics. The crystals are 200 nm thick with sub-nm surface roughness and a tunable lateral dimension of up to 200 μm. The molecular transitions remain narrow and spectrally stable, with inhomogeneous broadening below 100 GHz, comparable to DBT in bulk anthracene. The dopant density is tunable up to several hundred molecules per μm 2, ensuring emitters within the near-field of nanophotonic structures. We demonstrate that the crystals can be micropositioned onto integrated photonic devices with the molecular dipole aligned to the optical mode. This approach opens a path toward on-chip single-photon sources and collective many-emitter effects.
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Keni et al. (2026) studied this question.
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