We applied time-resolved near-field optical microscopic measurements with ultrashort light pulses of ~16 fs duration to observe plasmon dephasing processes in single gold nanorods. The correlation widths of the time-resolved signals obtained at each position on the nanorods were broadened compared with the auto-correlation width of the pulse because of the plasmon lifetime.The correlation width maps of the rods showed spatially oscillating patterns that look similar to the plasmon mode structures observed in the static near-field optical images. The spatial variation of the correlation widths was explained as arising from the position dependent contribution of the resonant plasmon excitation in the time-resolved signals relative to that of the non-resonant excitation. This finding indicates that the dephasing times of the resonant plasmon modes were constant regardless of the excitation position. This result is understood to be a consequence of the spatial coherence of the plasmon mode that causes the local excitation to be immediately delocalized across the rod after irradiation. A comparison between the timeresolved signals of the inner parts and the outer parts of the nanorods suggests that the nonresonant contribution to the time-resolved signals may be driven by the lower-order plasmon modes having resonances in a much longer wavelength region.

We investigated the spectral and spatial characteristics of plasmons induced in chemically synthesized triangular gold nano- and microplates by aperture-type scanning near-field optical microscopy. Near-field transmission images taken at plasmon resonance wavelengths showed two-dimensional oscillating patterns inside the plates. These spatial features were well reproduced by the square moduli of calculated eigen functions confined in the two-dimensional triangular potential well. From the irreducible representations of the eigen functions, it was found that both the out-of-plane modes and in-plane modes were clearly visualized in the near-field images. We compared near-field transmission images of a triangular nanoplate to those of a truncated one with a similar dimension and revealed that the fine details of the geometrical shape of the apex on the plate strongly influence the experimentally observed eigen mode structures. We also performed near-field transmission measurements of micrometer-scale triangular plates and found that wavy patterns were observed along the edges of the plates. The wavy features can be interpreted as the superposition of eigen modes with similar eigen energy. These findings prove that near-field transmission imaging enables one to directly visualize plasmonic eigen modes confined in the particle and provide fruitful information not only for a deeper understanding of plasmons but also for the application of the design and active control of plasmonic optical fields.

A detailed characterization of plasmon modes is important not only for a deeper understanding of plasmons but also for their practical applications. In this study, we investigated the three-dimensional near-field characteristics of high-order plasmon modes excited in a gold hexagonal nanoplate. From the near-field spectroscopic images, we found that both in-plane and out-of-plane plasmon modes observed near 900 nm were spectrally and spatially overlapped. We performed three-dimensional near-field measurement to reveal the optical characteristics of the overlapped modes in detail. We found that the steric near-field distribution near the nanoplate strongly depended on the plasmon mode, and the out-of-plane mode confines electromagnetic fields more tightly than the in-plane mode. We also found that the in-plane mode was dominantly visualized as the probe tip–sample distance increased. These findings demonstrate that the three-dimensional near-field technique enables selective visualization of a single plasmon mode even if multiple modes are spatially and spectrally overlapped.

We report a visible-light-induced copper-catalyzed highly enantioselective umpolung allylic acylation reaction with acylsilanes as acyl anion equivalents. Triplet-quenching experiments and DFT calculations supported our reaction design, which is based on copper-to-acyl metal-to-ligand charge transfer (MLCT) photoexcitation that generates a charge-separated triplet state as a highly reactive intermediate. According to the calculations, the allylic phosphate substrate in the excited state undergoes novel molecular activation into an allylic radical weakly bound to the copper complex. The allyl radical fragment undergoes copper-mediated regio- and stereocontrolled coupling with the acyl group under the influence of the chiral N-heterocyclic carbene ligand.

Precise understanding of the spatiotemporal characteristics of plasmons is essential for the development of applications of plasmonic nanoparticles. In this study, we investigated the spatiotemporal properties of high-order plasmon modes induced in a gold triangular nanoplate by static and dynamic near-field measurements. The near-field transmission measurements revealed that in-plane and out-of-plane polarized plasmon modes were simultaneously excited and these modes spectroscopically and spatially overlapped. The superposition of these modes was visualized in the near-field two-photon excitation image of the nanoplate. We performed time-resolved autocorrelation measurements on the nanoplate and found that the correlation width was broader than the excitation pulse due to the plasmon dephasing process. From the correlation width map of the nanoplate, we experimentally demonstrated that the out-of-plane plasmon mode exhibits a longer dephasing time than the in-plane plasmon mode. These findings indicate that the out-of-plane mode is desirable for improving the performance of plasmons in various applications.