Cavity quantum electrodynamics with single perovskite quantum dots

Fuente: arXiv
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Main Authors: Said, Zakaria, Trouche, Marina Cagnon, Borel, Antoine, Amara, Mohamed-Raouf, Reichel, Jakob, Voisin, Christophe, Diederichs, Carole, Chassagneux, Yannick
Format: Preprint
Published: 2025
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author Said, Zakaria
Trouche, Marina Cagnon
Borel, Antoine
Amara, Mohamed-Raouf
Reichel, Jakob
Voisin, Christophe
Diederichs, Carole
Chassagneux, Yannick
author_facet Said, Zakaria
Trouche, Marina Cagnon
Borel, Antoine
Amara, Mohamed-Raouf
Reichel, Jakob
Voisin, Christophe
Diederichs, Carole
Chassagneux, Yannick
contents Quantum emitters of single indistinguishable photons play a key role in quantum technologies. Among condensed matter systems, colloidal perovskite quantum dots have emerged as promising candidates, exhibiting high-purity single photon emission at room temperature and two-photon interference visibilities up to 0.5 at cryogenic temperatures. Achieving deterministic coupling of individual perovskite quantum dots to photonic structures is now a critical step towards harnessing cavity quantum electrodynamics (cQED) effects, such as the Purcell effect, to enhance single photon emission rate and indistinguishability. Here, we demonstrate the deterministic and reversible coupling of individual CsPbBr$_{3}$ perovskite quantum dots to a tunable, high-quality factor, low mode volume fiber-based Fabry-Pérot microcavity at 10~\si{\kelvin}. By spatially and spectrally tuning the cavity mode in resonance with the quantum dot emission, we observe up to a twofold increase in single photon emission rates. We build on the original multiplet excitonic fine structure to assess the vacuum Rabi coupling strength ($g \simeq$ 40~\si{\micro eV}) from the shaping of the spectral profile of the emission upon increasing the electromagnetic confinement. This approach also made it possible to delineate the contributions of spectral diffusion and pure dephasing to the total linewidth of emission, paving the way to a fully optimized control of the emission properties of cavity coupled perovskite quantum dots.
format Preprint
id arxiv_https___arxiv_org_abs_2503_20411
institution arXiv
publishDate 2025
record_format arxiv
spellingShingle Cavity quantum electrodynamics with single perovskite quantum dots
Said, Zakaria
Trouche, Marina Cagnon
Borel, Antoine
Amara, Mohamed-Raouf
Reichel, Jakob
Voisin, Christophe
Diederichs, Carole
Chassagneux, Yannick
Quantum Physics
Quantum emitters of single indistinguishable photons play a key role in quantum technologies. Among condensed matter systems, colloidal perovskite quantum dots have emerged as promising candidates, exhibiting high-purity single photon emission at room temperature and two-photon interference visibilities up to 0.5 at cryogenic temperatures. Achieving deterministic coupling of individual perovskite quantum dots to photonic structures is now a critical step towards harnessing cavity quantum electrodynamics (cQED) effects, such as the Purcell effect, to enhance single photon emission rate and indistinguishability. Here, we demonstrate the deterministic and reversible coupling of individual CsPbBr$_{3}$ perovskite quantum dots to a tunable, high-quality factor, low mode volume fiber-based Fabry-Pérot microcavity at 10~\si{\kelvin}. By spatially and spectrally tuning the cavity mode in resonance with the quantum dot emission, we observe up to a twofold increase in single photon emission rates. We build on the original multiplet excitonic fine structure to assess the vacuum Rabi coupling strength ($g \simeq$ 40~\si{\micro eV}) from the shaping of the spectral profile of the emission upon increasing the electromagnetic confinement. This approach also made it possible to delineate the contributions of spectral diffusion and pure dephasing to the total linewidth of emission, paving the way to a fully optimized control of the emission properties of cavity coupled perovskite quantum dots.
title Cavity quantum electrodynamics with single perovskite quantum dots
topic Quantum Physics
url https://arxiv.org/abs/2503.20411