We experimentally realize nano-antennas based on hybrid silicon-gold nanoparticles (NPs). The silicon particles covered by clusters of small metal NPs are fabricated from a liquid phase under the effect of the laser irradiation. The complex nanoclusters containing both Si and Au components provide the enhancement of the near-field intensity and the resonant light scattering associated with excitation of multipole resonances in NPs. A strong sensitivity of the resonant light absorption to the hybrid particle size and material parameters is experimentally documented and theoretically discussed. The results demonstrate a high potentiality of the hybrid NPs for the realization of functional optical devices and metasurfaces.

We show that the laser ablation method can be efficiently employed for the synthesis of silicon nanoparticles (NP), which are characterized by a strong resonant optical response in the visible spectral range. A single layer composed of silicon NPs has been deposited from the colloidal solution generated by laser ablation. The formation of hybrid silicon-gold NPs as a result of the laser action on a mixed colloidal solution is observed. These hybrid NPs are characterized by broadening of the near-field photoluminescence spectra compared to pure silicon NPs. These results may be used for the realization of functional metasurfaces consisting of randomly distributed resonant NPs.

We stabilize monoatomic carbon chains in water by attaching them to gold nanoparticles (NPs) by means of the laser ablation process. Resulting nanoobjects represent pairs of NPs connected by multiple straight carbon chains of several nanometer lengths. If NPs at the opposite ends of a chain differ in size, the structure acquires a dipole moment due to the difference in work functions of the two NPs. We take advantage of the dipole polarisation of carbon chains for ordering them by the external electric field. We deposit them on a glass substrate by the sputtering method in the presence of static electric fields of magnitudes up to 10⁵ V/m. The formation of one-dimensional carbyne quasi-crystals deposited on a substrate is evidenced by high-resolution TEM and X-ray diffraction measurements. The original kinetic model describing the dynamics of ballistically flowing nano-dipoles reproduces the experimental diagram of orientation of the deposited chains.