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We synthesized a mixture composed of gold nanoparticles of various shapes using the wet chemistry method. The final solution contained long nanorods, balls, disks and different spherical nanoparticles. To separate particles of individual shapes from the reaction mixture, the solution was centrifuged in a glucose density gradient. A distribution of nanoparticles based on their diameters was observed and each section was collected independently and each type of nanoobjects was characterised separately. Finally, the difference in nanoparticle shapes depending on the presence of Ag+ ions in the growth solution is reported and its influence on the separation is discussed.

Both nonlinear absorption and nonlinear refraction are effects that are potentially useful for a plethora of applications in photonics, nanophotonics and biophotonics. Despite substantial attention given to these phenomena by researchers studying the merits of disparate systems such as organic materials, hybrid materials, metal-containing molecules and nanostructures, it is virtually impossible to compare the results obtained on different materials when varying parameters of the light beams and different techniques are employed. We have attempted to address the problem by studying the properties of various systems in a systematic way, within a wide range of wavelengths, and including the regions of onephoton, two-photon and three-photon absorption. The objects of our studies have been typical nonlinear chromophores, such as π-conjugated molecules, oligomers and polymers, organometallics and coordination complexes containing transition metals, organometallic dendrimers, small metal-containing clusters, and nanoparticles of various kinds, including semiconductor quantum dots, plasmonic particles and rare-earth doped nanocrystals. We discuss herein procedures to quantify the nonlinear response of all of these systems, by defining and comparing the merit factors relevant for various applications.

The Z-scan technique was used to determine the spectral dependence of the nonlinear absorption in well-known DNA intercalators: ethidium bromide and its homodimer. It is found that the compounds show essentially the same features of their nonlinear absorption spectra with the magnitudes of the relevant cross sections scaling with molecular weight of chromophore compound.

A quantitative comparison of third-order nonlinear optical properties of colloidal gold nanoshells (NSs) and gold nanorods (NRs) in water solutions has been carried out using open- and closed-aperture Z-scan measurements, performed with femtosecond laser pulses over a broad range of wavelengths. Absorption saturation was found to be a dominant effect for all the studied nanoparticles; however, two-photon absorption (2PA) properties were also detected, and were clearly resolved especially at the shortest wavelengths used. The value of the merit factor σ2/M (2PA cross section scaled by the molecular weight) for the NRs (10×35 nm) at 530 nm is 7.5 (GM·mol/g), while for the NSs it is 1.9 (GM·mol/g) at the same wavelength.

We show how a single gold nanorod can serve as a multifunctional probe in an organized DNA matrix. Polarization analysis of two-photon luminescence excited with a femtosecond laser enables imaging of the orientation of a single nanorod, which reports the orientation of DNA strands. Carefully controlled photoinduced heating by the same laser is able to degrade the DNA matrix in a highly localized volume.

Deoxyribonucleic acid (DNA) chains can be engineered for diverse nanophotonics applications by the insertion of molecular groups in different spatial configurations. DNA chains can be assembled into wire-like structures, origami structures, photonic crystal-like assemblies, liquid-crystal phases, and thin films. These structures can be made to serve as scaffolds for the organization of various organic molecules and nanoparticles. The properties of nanostructures can be modified by the use of DNA and DNA modified by the surfactants.

Amyloid fibrils are peptide or protein aggregates possessing a cross-β-sheet structure. They possess intrinsic fluorescence property, which is still not fully understood. Herein, we compare structural and optical properties of fibrils formed from L- and D-enantiomers of the (105-115) fragment of transthyretin (TTR) and from their racemic mixture. Our results show that autofluorescence of fibrils obtained from enantiomers differs from that of fibrils from the racemic mixture. In order to elucidate the origin of observed differences, we analyzed the structure and morphology of fibrils and showed how variations in β-sheet organization influence optical properties of fibrils. We clarified the contribution of aromatic rings and the amyloid backbone to the final blue-green emission of fibrils. This work demonstrates how enantiomeric composition of amino acids allows us to modulate the self-assembly and final morphology of well-defined fibrillar bionanostructures with optical properties controlled by supramolecular organization.