Nanophotonic Enhancement of the Forster Resonance Energy-Transfer Rate with Single Nanoapertures

被引:91
作者
Ghenuche, Petru [1 ]
de Torres, Juan [1 ]
Moparthi, Satish Babu [1 ]
Grigoriev, Victor [1 ]
Wenger, Jerome [1 ]
机构
[1] Aix Marseille Univ, CNRS, Cent Marseille, Inst Fresnel,UMR 7249, F-13013 Marseille, France
关键词
FRET; plasmonics; LDOS; metal nanoaperture; zero mode waveguide; fluorescence enhancement; MODE WAVE-GUIDES; MOLECULE FLUORESCENCE; SPONTANEOUS EMISSION; DEPENDENCE; EFFICIENCY; DYNAMICS; DISTANCE; ANTENNAS; DONOR;
D O I
10.1021/nl5018145
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Tailoring the light matter interaction and the local density of optical states (LDOS) with nanophotonics provides accurate control over the luminescence properties of a single quantum emitter. This paradigm is also highly attractive to enhance the near-field Forster resonance energy transfer (FRET) between two fluorescent emitters. Despite the wide applications of FRET in nanosciences, using nanophotonics to enhance FRET has remained a debated and complex challenge. Here we demonstrate enhanced energy transfer within single donor acceptor fluorophore pairs confined in single gold nanoapertures. Experiments monitoring both the donor and the acceptor emission photodynamics clearly establish a linear dependence of the FRET rate on the LDOS in nanoapertures, demonstrating that nanophotonics can be used to intensify the near-field energy transfer. Strikingly, we observe a significant six-fold increase in the FRET rate for large donor acceptor separations exceeding 13 nm. Exciting opportunities are opened to investigate biochemical structures with donor acceptor distances much beyond the classical Forster radius. Importantly, our approach is fully compatible with the detection of single biomolecules freely diffusing in water solution under physiological conditions.
引用
收藏
页码:4707 / 4714
页数:8
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