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

被引:54
作者
Bidault, Sebastien [1 ]
Devilez, Alexis [2 ]
Maillard, Vincent [1 ]
Lermusiaux, Laurent [1 ]
Guigner, Jean-Michel [3 ]
Bonod, Nicolas [2 ]
Wenger, Jerome [2 ]
机构
[1] PSL Res Univ, CNRS, INSERM, Inst Langevin,ESPCI Paris, 1 Rue Jussieu, F-75005 Paris, France
[2] Aix Marseille Univ, CNRS, UMR 7249, Inst Fresnel,Cent Marseille, F-13013 Marseille, France
[3] Univ Paris 06, Sorbonne Univ, CNRS, MNHN,IMPMC,IRD UMR 206,UMR 7590, Paris, France
关键词
self-assembled nanostructures; plasmon-enhanced fluorescence; single-photon emission; fluorescence correlation spectroscopy; dark-field microscopy; MOLECULE FLUORESCENCE; SPONTANEOUS EMISSION; ENHANCEMENT; NANOANTENNAS; PHOTOSTABILITY; NANOPARTICLES; EXCITATION; EXCITONS; EMITTERS;
D O I
10.1021/acsnano.6b01729
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
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.
引用
收藏
页码:4806 / 4815
页数:10
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