Model-Based Insight into Single-Molecule Plasmonic Mislocalization

被引:2
|
作者
Zuo, Tiancheng [1 ]
Goldwyn, Harrison J. [2 ]
Masiello, David J. [2 ]
Biteen, Julie S. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
[2] Univ Washington, Dept Chem, Seattle, WA 98195 USA
来源
JOURNAL OF PHYSICAL CHEMISTRY C | 2021年 / 125卷 / 44期
基金
美国国家科学基金会;
关键词
FLUORESCENCE; DNA; ENHANCEMENT; MICROSCOPY; DYE; NANOPARTICLES; DISTORTION; NANOSCALE; IMAGES;
D O I
10.1021/acs.jpcc.1c07989
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Noble metal nanoparticles act as visible-wavelength antennas that reshape the emission of nearby dye molecules. Because single-molecule imaging overcomes ensemble averaging, it is uniquely suited for understanding these plasmonic effects. We have engineered single-particle assemblies consisting of a gold nanodisk surrounded by ATTO590 dye molecules attached by double-stranded DNA linkers. These assemblies provide a controlled geometry that places plasmon-coupled dye molecules at specific radial positions in the plane of the nanodisk and provides the ground truth actual dye molecule position for further analysis. We modeled the molecule-nanoantenna interaction as two coupled dipoles and propagated their interfering fields through a diffraction-limited microscope to generate a coupled-dipole image that accurately recreates the distorted PSFs seen in numerical simulations of plasmon-enhanced single-molecule fluorescence. We fit simulated and experimental data to the model function as well as to a standard Gaussian function and evaluated the advantages of the model approach. Overall, we find that the image model can better recapture certain aspects of the dye molecule mislocalization, and we propose that remaining gaps can be addressed by integrating higher-order plasmon multipole effects into the nanodisk response as well as by simultaneously using both image and spectral information.
引用
收藏
页码:24531 / 24539
页数:9
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