The experimentally determined scattering spectra of discrete, crystalline, gold nanorod dimers arranged side-to-side, end-to-end, at right angles in different orientations and also with longitudinal offsets are reported along with the electron micrographs of the individual dimers. The spectra exhibit both red-and blue-shifted surface plasmon resonances, consistent with the plasmon hybridization model. However, the plasmon coupling constant for gold dimers with less than a few nanometers separation between the particles does not obey the exponential dependence predicted by the Universal Plasmon Ruler equation. The experimentally determined spectra are compared with electrodynamic calculations and the interactions between the individual rod plasmons in different dimer orientations are elucidated.

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We present experimental data on the light scattering properties of linear chains of gold nanoparticles with up to six nanoparticles and an interparticle spacing of 1 nm. A red shift of the surface plasmon resonance with increasing chain length is observed. An exponential model applied to the experimental data allows determination of an asymptotic maximum resonance at a chain length of 10-12 particles. The optical data are compared with analytical and numerical calculation methods (EEM and BEM).