We demonstrate a far-field single molecule super-resolution method that maps plasmonic near-fields. The method is largely invariant to fluorescence quenching (arising from probe proximity to a metal), has reduced point-spread-function distortion compared to fluorescent dyes (arising from strong coupling to nanoscopic metallic features), and has a large dynamic range (of 2 orders of magnitude) allowing mapping of plasmonic field-enhancements regions. The method takes advantage of the sensitivity of quantum dot (QD) stochastic blinking to plasmonic near-fields. The modulation of the blinking characteristics thus provides an indirect measure of the local field strength. Since QD blinking can be monitored in the far-field, the method can measure localized plasmonic near-fields at high throughput using a simple far-field optical setup. Using this method, propagation lengths and penetration depths were mapped-out for silver nanowires of different diameters and for different dielectric environments, with a spatial accuracy of ∼15 nm. We initially use sparse sampling to ensure single molecule localization for accurate characterization of the plasmonic near-field with plans to increase density of emitters in further studies. The measured propagation lengths and penetration depths values agree well with Maxwell finite-difference time-domain calculations and with published literature values. This method offers advantages such as low cost, high throughput, and superresolved mapping of localized plasmonic fields at high sensitivity and fidelity.
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http://dx.doi.org/10.1021/acsnano.6b03873 | DOI Listing |
In this Letter, we present a theoretical study based on the Lorentz function and harmonic oscillator model to explore temporal dynamics of charge transfer plasmon (CTP) resonances. By fitting scattering curves and near-field oscillations, we determine the dephasing time of CTP modes in conductively connected gold nanodisk dimers. We show that, compared with the well-known particle plasmon and dimer plasmon modes, the CTP mode has a narrow spectral width and longer lifetime.
View Article and Find Full Text PDFACS Nano
December 2024
Interdisciplinary Nanoscience Center, Aarhus University, Gustav Wieds Vej 14, Aarhus C 8000, Denmark.
Multivalency as an interaction principle is widely utilized in nature. It enables specific and strong binding by multiple weak interactions through enhanced avidity and is a core process in immune recognition and cellular signaling, which is also a current concept in drug design. Here, we use the high signals from plasmon-enhanced fluorescence of nanoparticles to extract binding kinetics and dynamics of multivalent interactions on the single-molecule level and in real time.
View Article and Find Full Text PDFNanophotonics
November 2024
Joint International Research Laboratory of Information Display and Visualization, School of Electronic Science and Engineering, Southeast University, Nanjing 210096, China.
Optical interconnects, leveraging surface plasmon modes, are revolutionizing high-performance computing and AI, overcoming the limitations of electrical interconnects in speed, energy efficiency, and miniaturization. These nanoscale photonic circuits integrate on-chip light manipulation and signal conversion, marking significant advancements in optoelectronics and data processing efficiency. Here, we present a novel plasmonic interconnect circuit, by introducing refractive index matching layer, the device supports both pure SPP and different hybrid modes, allowing selective excitation and transmission based on light wavelength and polarization, followed by photocurrent conversion.
View Article and Find Full Text PDFSmall
December 2024
Department of Chemistry, Yonsei University, Yonsei-ro 50, Seoul, 03722, Republic of Korea.
This study presents a synthesis method for Au tetrahedral nanoframes (Td NFs) through a rationally designed multiple-step process, followed by an investigation of their distinctively ordered self-assembly for enhanced performance in surface-enhanced Raman spectroscopy (SERS). Two distinct Au Td NF building blocks are synthesized, exhibiting mono-rim or dual-rim morphologies. The mono-rim structure lacks intra-nanogaps, whereas the dual-rim configuration features well-defined intra-nanogaps.
View Article and Find Full Text PDFNanophotonics
February 2024
School of Engineering, College of Engineering and Computer Science, Australian National University, Canberra, ACT 2601, Australia.
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