| Literature DB >> 29969274 |
Simeon I Bogdanov1,2, Mikhail Y Shalaginov1,2, Alexei S Lagutchev1,2, Chin-Cheng Chiang1,2, Deesha Shah1,2, Alexandr S Baburin3,4, Ilya A Ryzhikov3,5, Ilya A Rodionov3,4, Alexander V Kildishev1,2, Alexandra Boltasseva1,2, Vladimir M Shalaev1,2.
Abstract
Solid-state quantum emitters are in high demand for emerging technologies such as advanced sensing and quantum information processing. Generally, these emitters are not sufficiently bright for practical applications, and a promising solution consists in coupling them to plasmonic nanostructures. Plasmonic nanostructures support broadband modes, making it possible to speed up the fluorescence emission in room-temperature emitters by several orders of magnitude. However, one has not yet achieved such a fluorescence lifetime shortening without a substantial loss in emission efficiency, largely because of strong absorption in metals and emitter bleaching. Here, we demonstrate ultrabright single-photon emission from photostable nitrogen-vacancy (NV) centers in nanodiamonds coupled to plasmonic nanocavities made of low-loss single-crystalline silver. We observe a 70-fold difference between the average fluorescence lifetimes and a 90-fold increase in the average detected saturated intensity. The nanocavity-coupled NVs produce up to 35 million photon counts per second, several times more than the previously reported rates from room-temperature quantum emitters.Entities:
Keywords: Quantum plasmonics; epitaxial silver; nanodiamonds; nanopatch antennas; nitrogen-vacancy centers; single-photon source
Year: 2018 PMID: 29969274 DOI: 10.1021/acs.nanolett.8b01415
Source DB: PubMed Journal: Nano Lett ISSN: 1530-6984 Impact factor: 11.189