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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.

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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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Using a combination of Drude and critical points models, we show that the permittivity of several metals can be more efficiently described than using the well-known Drude–Lorentz model. The numerical implementation in a finite-difference time-domain code together with a non-uniform grid enables the study of thin metallic intermediate layers often neglected in simulations but found in realistic resonant structures.

Localized Surface Plasmons (LSP) on metallic nanoparticles of different shapes are investigated by extinction spectroscopy. Experimental results are compared to simulations by a Finite-Difference TimeDomain (FDTD) method. Three different shapes of nanoparticles are compared, oblates, prolates and ellipsoids, in terms of spectral tunability of the LSP resonance (LSPR). It is found that the complete geometry of the nanoparticle must be given to truly define the LSP resonance and that ellipsoids offer the widest spectral tunability.

We report on controlled nanoscale photopolymerization triggered by enhanced near fields of silver nanoparticles excited close to their dipolar plasmon resonance. By anisotropic polymerization, symmetry of the refractive index of the surrounding medium was broken: C infinity v symmetry turned to C2v symmetry. This allowed for spectral degeneracy breaking in particles plasmon resonance whose apparent peak became continuously tunable with the incident polarization. From the spectral peak, we deduced the refractive-index ellipsoid fabricated around the particles. In addition to this control of optical properties of metal nanoparticles, this method opens new routes for nanoscale photochemistry and provides a new way of quantification of the magnitude of near fields of localized surface plasmons.