Indistinguishable near infra-red single photons from an individual organic molecule
arXiv:1011.6152 · doi:10.1103/PhysRevA.82.063803
Abstract
By using the zero-phonon line emission of an individual organic molecule, we realized a source of indistinguishable single photons in the near infrared. A Hong-Ou-Mandel interference experiment is performed and a two-photon coalescence probability of higher than 50% at 2 K is obtained. The contribution of the temperature-dependent dephasing processes to the two-photon interference contrast is studied. We show that the molecule delivers nearly ideal indistinguishable single photons at the lowest temperatures when the dephasing is nearly lifetime limited. This source is used to generate post-selected polarization-entangled photon pairs, as a test-bench for applications in quantum information.
References in corpus (5)
- Tunable Indistinguishable Photons From Remote Quantum Dots
- Quantum Beat of Two Single Photons
- Indistinguishable photons from the resonance fluorescence of a single quantum dot in a microcavity
- Interference of Single Photons from Two Separate Semiconductor Quantum Dots
- Quantum Interference of Tunably Indistinguishable Photons from Remote Organic Molecules
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- Photon indistinguishability measurements under pulsed and continuous excitation
- Polymer-encapsulated organic nanocrystals for single photon emission
- Generation of polarization-entangled photon pairs from two interacting quantum emitters
- Sub-nanosecond coherent optical manipulation of a single aromatic molecule at cryogenic temperature
- Enhanced phonon lifetimes with optically controlled single molecules