Accessible hotspots for single-protein SERS in DNA-origami assembled gold nanorod dimers with tip-to-tip alignment.

The label-free identification of individual proteins from liquid samples by surface-enhanced Raman scattering (SERS) spectroscopy is a highly desirable goal in biomedical diagnostics. However, the small Raman scattering cross-section of most (bio-)molecules requires a means to strongly amplify their Raman signal for successful measurement, especially for single molecules. This amplification can be achieved in a plasmonic hotspot that forms between two adjacent gold nanospheres. However, the small (≈1-2 nm) gaps typically required for single-molecule measurements are not accessible for most proteins. A useful strategy would thus involve dimer structures with gaps large enough to accommodate single proteins, whilst providing sufficient field enhancement for single-molecule SERS. Here, we report on using a DNA origami scaffold for tip-to-tip alignment of gold nanorods with an average gap size of 8 nm. The gaps are accessible to streptavidin and thrombin, which are captured at the plasmonic hotspot by specific anchoring sites on the origami template. The field enhancement achieved for the nanorod dimers is sufficient for single-protein SERS spectroscopy with sub-second integration times. This design for SERS probes composed of DNA origami with accessible hotspots promotes future use for single-molecule biodiagnostics in the near-infrared range.

Single-Step Plasmonic Dimer Printing by Gold Nanorod Splitting with Light.

Optical printing is a flexible strategy to precisely pattern plasmonic nanoparticles for the realization of nanophotonic devices. However, the generation of strongly coupled plasmonic dimers by sequential particle printing can be a challenge. Here, we report an approach to generate and pattern dimer nanoantennas in a single step by optical splitting of individual gold nanorods with laser light. We show that the two particles that constitute the dimer can be separated by sub-nanometer distances. The nanorod splitting process is explained by a combination of plasmonic heating, surface tension, optical forces, and inhomogeneous hydrodynamic pressure introduced by a focused laser beam. This realization of optical dimer formation and printing from a single nanorod provides a means for dimer patterning with high accuracy for nanophotonic applications.

Monitoring the surface quality of silver plasmon waveguides with nonlinear photoemission electron microscopy and in-situ ion sputtering.

We use photoemission electron microscopy (PEEM) with single- and two-photon excitation to study the properties of surface plasmon polaritons (SPPs) in tapered silver stripe waveguides. Arrays of waveguides with different widths, grating coupler geometries, and taper angles are fabricated using electron beam lithography (EBL) on Si and indium-tin-oxide (ITO)-covered glass substrates. The presence of propagating SPP modes is indicated by modulations of the non-linear photoemission intensity which run along the length of the waveguide - the result of interfering SPPs reflected from the edges. Surface roughness also results in the presence of random emission hot spots and strong edge diffraction, which hinders an analysis of the effect of waveguide geometry on SPP propagation length and nanofocusing. Accordingly, we develop a relatively simple, in-situ method of reducing the surface roughness by argon ion sputtering using low-energy (∼ 300eV) ions. Surface roughness is qualitatively assessed by the ratio of the photoemission from the central interference fringes to that from the edges, and from the hot spot intensity. The improvement of the surface quality is a critical step for reducing radiative losses and therefore increasing the propagation length of plasmonic waveguides.