
1.State Key Laboratory of Surface Physics and Department of Physics, Fudan University, Shanghai 200433, China
2.Shanghai Institute for Advanced Communication and Data Science, Shanghai University, Shanghai 200444, China
3.Key Laboratory of Specialty Fiber Optics and Optical Access Networks, Joint International Research Laboratory of Specialty Fiber Optics and Advanced Communication, Shanghai University, Shanghai 200444, China
4.Department of Chemistry and State Key Laboratory of Molecular Engineering of Polymers, Fudan University, Shanghai 200433, China
5.Institute for Nanoelectronic Devices and Quantum Computing, Fudan University, Shanghai 200433, China
6.Collaborative Innovation Center of Advanced Microstructures, Nanjing 210093, China
7.Multiscale Research Institute of Complex Systems, Fudan University, Shanghai 200433, China
Lei Zhou (phzhou@fudan.edu.cn)
Yan-Wen Tan (ywtan@fudan.edu.cn)
Published:31 May 2021,
Published Online:14 April 2021,
Received:18 October 2020,
Revised:13 March 2021,
Accepted:29 March 2021
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Zhao, W. Q. et al. Engineering single-molecule fluorescence with asymmetric nano-antennas. Light: Science & Applications, 10, 858-866 (2021).
Zhao, W. Q. et al. Engineering single-molecule fluorescence with asymmetric nano-antennas. Light: Science & Applications, 10, 858-866 (2021). DOI: 10.1038/s41377-021-00522-9.
As a powerful tool for studying molecular dynamics in bioscience
single-molecule fluorescence detection provides dynamical information buried in ensemble experiments. Fluorescence in the near-infrared (NIR) is particularly useful because it offers higher signal-to-noise ratio and increased penetration depth in tissue compared with visible fluorescence. The low quantum yield of most NIR fluorophores
however
makes the detection of single-molecule fluorescence difficult. Here
we use asymmetric plasmonic nano-antenna to enhance the fluorescence intensity of AIEE1000
a typical NIR dye
by a factor up to 405. The asymmetric nano-antenna achieve such an enhancement mainly by increasing the quantum yield (to ~80%) rather than the local field
which degrades the molecules' photostability. Our coupled-mode-theory analysis reveals that the enhancements stem from resonance-matching between antenna and molecule and
more importantly
from optimizing the coupling between the near- and far-field modes with designer asymmetric structures. Our work provides a universal scheme for engineering single-molecule fluorescence in the near-infrared regime.
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