ABSTRACT
An experimental three dimensional characterization of the local refractive index sensitivity of plasmonic gold nanorods is performed by controlled apposition of lithographic nanostructures. We show up to seven times higher sensitivity values to local changes in the refractive index at the particle tip than center. In addition, successive deposition of defined nm-thin dielectric layers on nanorods covered with stripe masks allows us to study the sensitivity decrease normal to the particle surface separately for different particle sites. Clear trends to a stronger sensitivity decay at sites of higher local sensitivity are demonstrated experimentally and theoretically. Our sensitivity characterization provides an important tool to find the most suitable particle type and particle site for specific bio-sensing applications.
Subject(s)
Nanotubes/chemistry , Biosensing Techniques , Gold/chemistry , Metal Nanoparticles/chemistry , Microscopy, Electron, Scanning , Polymethyl Methacrylate/chemistry , Quartz Crystal Microbalance Techniques , Silicon Dioxide/chemistry , Surface Plasmon ResonanceABSTRACT
The spontaneous emission rate of a fluorophore provides a direct probe of the photonic local density of states at the fluorophore position. Here we exploit this capability to map the plasmonic modes of gold nanoparticles by imaging the fluorescence intensity in combined regular arrays of identical gold and fluorophore-doped polymer nanoparticles. By varying the distance between gold and polymer particles across the array, the fluorophore emission generates an optical Moiré pattern corresponding to a magnified spatial map of the plasmonic mode, which can be directly imaged with an optical microscope. Our results are corroborated by supplementary theoretical model calculations.
ABSTRACT
We investigate experimentally and theoretically few-particle effects in the optical spectra of single quantum dots (QDs). Photodepletion of the QD together with the slow hopping transport of impurity-bound electrons back to the QD are employed to efficiently control the number of electrons present in the QD. By investigating structurally identical QDs, we show that the spectral evolutions observed can be attributed to intrinsic, multi-particle-related effects, as opposed to extrinsic QD-impurity environment-related interactions. From our theoretical calculations we identify the distinct transitions related to excitons and excitons charged with up to five additional electrons, as well as neutral and charged biexcitons.
