Nanophotonic Fabrication for Coupling to Single Organic Molecules

Dibenzoterrylene (DBT) is a polycyclic-aromatic hydrocarbon (C<inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">38</inf>H<inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">20</inf>) that displays Fourier-limited (≈40 MHz), fast (decay lifetime of 3.6 ns) and stable photon emission with an inhomogeneous distribution centered around 785 nm when hosted in a uniform anthracene crystal held at cryogenic temperature (< 4 K) [1]. It demonstrates near-unity quantum efficiency with ≈ 50% of all emissive pathways going via the narrow and coherent zero-phonon line (ZPL). Additionally, the ZPL lies close to resonance with rubidium transitions, making it compatible with atomic quantum technologies [2]. However, poor collection efficiencies and limited emission rates restrict the use of DBT as a single-photon source. This can be overcome by coupling DBT to nanophotonic structures, leading to preferential emission into a single photonic mode at an enhanced rate due to the Purcell effect.

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Published
2025-06-23
DOI
https://doi.org/10.1109/cleo/europe-eqec65582.2025.11110355
Primary Topic
Photonic and Optical Devices
Type
article
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article

Nanophotonic Fabrication for Coupling to Single Organic Molecules

Rowan A. Hoggarth, Alex S. Clark, Jieqing Mo, Michael J. Neville et al.
Photonic and Optical Devices
article

Nanophotonic Fabrication for Coupling to Single Organic Molecules

Rowan A. Hoggarth, Alex S. Clark, Jieqing Mo, Michael J. Neville, Granthick Barua
article en

Abstract

Dibenzoterrylene (DBT) is a polycyclic-aromatic hydrocarbon (C<inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">38</inf>H<inf xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink">20</inf>) that displays Fourier-limited (≈40 MHz), fast (decay lifetime of 3.6 ns) and stable photon emission with an inhomogeneous distribution centered around 785 nm when hosted in a uniform anthracene crystal held at cryogenic temperature (< 4 K) [1]. It demonstrates near-unity quantum efficiency with ≈ 50% of all emissive pathways going via the narrow and coherent zero-phonon line (ZPL). Additionally, the ZPL lies close to resonance with rubidium transitions, making it compatible with atomic quantum technologies [2]. However, poor collection efficiencies and limited emission rates restrict the use of DBT as a single-photon source. This can be overcome by coupling DBT to nanophotonic structures, leading to preferential emission into a single photonic mode at an enhanced rate due to the Purcell effect.

University of Bristol (GB)
Openalex Percentile: Top 79%
Photonic and Optical Devices
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Nanophotonic Fabrication for Coupling to Single Organic Molecules — Rowan A. Hoggarth, Alex S. Clark, et al. · (2025) | TGRS Research Map | TGRS