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Picosecond Lifetimes with High Quantum Yields from Single-Photon-Emitting Colloidal Nanostructures at Room
Sébastien Bidault1, Alexis Devilez2, Vincent Maillard1
1ESPCI Paris, PSL Research University, CNRS, INSERM, Institut Langevin , 1 Rue Jussieu, F-75005 Paris, France.
ACS Nano
|March 15, 2016
Summary
Researchers created bright, single-photon emitting gold nanoparticle dimers using DNA. These nanostructures show short luminescence lifetimes below 10 ps and high quantum yields, enabling efficient light sources.
Area of Science:
- Nanophotonics
- Quantum Optics
- Biomolecular Engineering
Background:
- Optimizing solid-state light sources requires minimizing luminescence lifetime and maximizing quantum yield.
- Nonradiative processes significantly impact performance at room temperature.
- Fluorescent molecules coupled with plasmonic nanostructures offer enhanced optical properties.
Purpose of the Study:
- To demonstrate DNA-templated gold nanoparticle dimers as efficient single-photon emitters.
- To achieve ultrashort luminescence lifetimes and high quantum yields in nanostructure-based light sources.
- To enable parallel production of millions of bright fluorescent nanostructures.
Main Methods:
- Fabrication of 60 and 80 nm gold nanoparticle dimers templated by DNA.
- Incorporation of single fluorescent molecules within the nanoparticle dimers.
- Characterization using fluorescence spectroscopy on fixed and diffusing nanostructures.
- Quantitative estimation of decay rate and fluorescence intensity distributions.
Main Results:
- Achieved single-photon emission with luminescence lifetimes below 10 picoseconds (ps).
- Observed typical quantum yields in the range of 45-70%.
- Demonstrated excellent agreement between experimental data and theoretical calculations.
- Showcased parallel production of millions of bright nanostructures with radiative lifetimes under 100 ps.
Conclusions:
- DNA-templated gold nanoparticle dimers are effective for creating efficient single-photon emitters.
- Ultrashort luminescence lifetimes and high quantum yields are achievable, surpassing limitations of nonradiative decay.
- The developed method allows for scalable, parallel synthesis of advanced fluorescent nanostructures for light-source applications.

