4.8 Article

Picosecond Lifetimes with High Quantum Yields from Single-Photon-Emitting Colloidal Nanostructures at Room Temperature

Journal

ACS NANO
Volume 10, Issue 4, Pages 4806-4815

Publisher

AMER CHEMICAL SOC
DOI: 10.1021/acsnano.6b01729

Keywords

self-assembled nanostructures; plasmon-enhanced fluorescence; single-photon emission; fluorescence correlation spectroscopy; dark-field microscopy

Funding

  1. Agence Nationale de la Recherche [ANR 11 BS10 002 02, ANR 11 JS10 002 01]
  2. LABEX WIFI (Laboratory of Excellence within the French Program Investments for the Future) [ANR-10-LABX-24, ANR-10-IDEX-0001-02 PSL*]
  3. Region Ile-de-France
  4. European Commission [ERC StG 278242]
  5. A*MIDEX project - Investissements d'Avenir French Government program [ANR-11-IDEX-0001-02]

Ask authors/readers for more resources

Minimizing the luminescence lifetime while maintaining a high emission quantum yield is paramount in optimizing the excitation cross-section, radiative decay rate, and brightness of quantum solid-state light sources, particularly at room temperature, where nonradiative processes can dominate. We demonstrate here that DNA-templated 60 and 80 nm diameter gold nanoparticle dimers, featuring one fluorescent molecule, provide single-photon emission with lifetimes that can fall below 10 ps and typical quantum yields in a 45-70% range. Since these colloidal nanostructures are obtained as a purified aqueous suspension, fluorescence spectroscopy can be performed on both fixed and freely diffusing nanostructures to quantitatively estimate the distributions of decay rate and fluorescence intensity enhancements. These data are in excellent agreement with theoretical calculations and demonstrate that millions of bright fluorescent nanostructures, with radiative lifetimes below 100 ps, can be produced in parallel.

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