The optical trapping of Au nanoparticles with dimensions as small as 10 nm in the gap of plasmonic dipole antennas is demonstrated. Single nanoparticle trapping events are recorded in real time by monitoring the Rayleigh scattering spectra of individual plasmonic antennas. Numerical simulations are also performed to interpret the experimental results, indicating the possibility to trap nanoparticles only a few nanometers in size. This work unveils the potential associated with the integration of plasmonic trapping with localized surface plasmon resonance based sensing techniques, in order to deliver analyte to specific, highly sensitive regions ("hot spots").
We present single molecule tip-enhanced resonance Raman spectra from brilliant cresyl blue (BCB) submonolayers adsorbed on a planar Au surface with Ag tips. A gap of 1 nm between a Ag tip and the Au substrate was employed to create a highly enhanced electric field and to generate Raman scattering from an area of ∼100 nm 2 . Three lines of evidence are presented to prove the single molecule sensitivity of our experiments: (1) Extremely diluted samples were used. Estimations show that at most a few molecules were excited by the Ag tip. (2) Spectroscopic fluctuations, including intensity fluctuations, frequency shifts, and line shape changes were observed. A histogram analysis of the intensity fluctuations of two different BCB coverages was carried out. The results clearly show the features of single molecule behavior. (3) Discrete signal losses also were observed. This is because of photochemical processes involving single molecules. Besides BCB, which shows a strong resonant absorption at 633 nm (the wavelength of the excitation laser), a self-assembled monolayer of benzenethiol, which does not strongly absorb at 633 nm, was studied. Good quality spectra were recorded with a short exposure time (10 s) and time-dependent spectral changes were also observed.
Plasmon‐enhanced upconversion luminescence of NaYF4: Yb3+/Er3+ co‐doped nanocrystals is investigated using a 3D plasmonic antenna architecture: a disk‐coupled dots‐on‐pillar antenna array (D2PA). By tuning and optimizing the resonance frequency of the D2PA structure for upconversion luminescence, a 310‐fold luminescence enhancement and an 8‐fold reduction of the luminescence decay time are observed.
We studied the influence of nanosteps on signal intensity in gap-mode tip-enhanced Raman spectroscopy (TERS). A benzenethiol monolayer adsorbed on an Au substrate was investigated. The correlation between the TERS signal and the local topography on the substrate shows that a 2 nm high sharp step on the Au surface can significantly increase the enhancement. Furthermore, theoretical models were built, and the numerical simulation results were consistent with our experimental results. The findings provide evidence that nanoscale roughness can play a crucial role in the "hot sites" corresponding to single-molecule surface-enhanced Raman spectroscopy (SERS).
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