DNA Origami Substrates for Highly Sensitive Surface-Enhanced Raman Scattering

DNA nanotechnology holds great promise for the fabrication of novel plasmonic nanostructures and the potential to carry out single-molecule measurements using optical spectroscopy. Here, we demonstrate for the first time that DNA origami nanostructures can be exploited as substrates for surface-enhanced Raman scattering (SERS). Gold nanoparticles (AuNPs) have been arranged into dimers to create intense Raman scattering hot spots in the interparticle gaps. AuNPs (15 nm) covered with TAMRA-modified DNA have been placed at a nominal distance of 25 nm to demonstrate the formation of Raman hot spots. To control the plasmonic coupling between the nanoparticles and thus the field enhancement in the hot spot, the size of AuNPs has been varied from 5 to 28 nm by electroless Au deposition. By the precise positioning of a specific number of TAMRA molecules in these hot spots, SERS with the highest sensitivity down to the few-molecule level is obtained

Polarization- and Wavelength-Dependent Surface-Enhanced Raman Spectroscopy Using Optically Anisotropic Rippled Substrates for Sensing

Anisotropic Ag nanoparticle arrays were created by metal evaporation on rippled silicon templates for sensing of molecules with surface-enhanced Raman spectroscopy. Our results show that these substrates can be used for analysis of complex molecular mixtures and discrimination of solvent molecules. These properties are due to their polarization and wavelength dependency that provide enhancement in a wide spectral range. The dielectric function parallel and perpendicular to the long axis of the nanostructures was determined via ellipsometry yielding two different plasmonic resonances. Polarized surface-enhanced raman scattering (SERS) was subsequently measured as a function of the polarization angle θ for a 4-mercaptobenzonitrile self-assembled monolayer covalently attached to the Ag surface. For 514 nm excitation a cos² θ-dependence and for 647 nm excitation a sin² θ-dependency were found, with the maxima expressing the resonances perpendicular and parallel to the ripples, respectively. Those results open the path for using such a substrate as a chemical sensor providing strong enhancement in a broad range of laser wavelengths on only one sensing surface and increasing the specificity by matching resonant Raman conditions