The sub-diffraction imaging of the optical near-field in nanostructures, based on a photochemical technique, is reported. A photosensitive azobenzene-dye polymer is spin coated onto lithographic structures and is subsequently irradiated with laser light. Photoinduced mass transport creates topographic modifications at the polymer film surface that are then measured with atomic force microscopy (AFM). The AFM images correlate with rigorous theoretical calculations of the near-field intensities for a range of different nanostructures and illumination polarizations. This approach is a first step toward additional methods for resolving confined optical near fields, which can augment scanning probe methodologies for high spatial resolution of optical near fields.
We report on the emission of hybrid nanosources composed of gold nanoparticles coupled with quantum dots. The emission relies on energy transfer from the quantum dots to gold nanoparticles which could be de-excited through radiative plasmon relaxation. The dependence of the emission efficiency is studied systematically as a function of the size of gold nanoparticles and interdistance between gold nanoparticles and quantum dots. We demonstrate a size-dependent transition between quenching and enhancement and a nonradiative energy transfer from the quantum dots to the gold nanoparticles.
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