A new class of tunable hypersonic phononic crystals based on polymer-tethered colloids.

The design and engineering of hybrid materials exhibiting tailored phononic band gaps are fundamentally relevant to innovative material technologies in areas ranging from acoustics to thermo-optic devices. Phononic hybridization gaps, originating from the anti-crossing between local resonant and propagating modes, have attracted particular interest because of their relative robustness to structural disorder and the associated benefit to 'manufacturability'. Although hybridization gap materials are well known, their economic fabrication and efficient control of the gap frequency have remained elusive because of the limited property variability and expensive fabrication methodologies. Here we report a new strategy to realize hybridization gap materials by harnessing the 'anisotropic elasticity' across the particle-polymer interface in densely polymer-tethered colloidal particles. Theoretical and Brillouin scattering analysis confirm both the robustness to disorder and the tunability of the resulting hybridization gap and provide guidelines for the economic synthesis of new materials with deliberately controlled gap position and width frequencies.

Collective hypersonic excitations in strongly multiple scattering colloids.

Unprecedented low-dispersion high-frequency acoustic excitations are observed in dense suspensions of elastically hard colloids. The experimental phononic band structure for SiO(2) particles with different sizes and volume fractions is well represented by rigorous full-elastodynamic multiple-scattering calculations. The slow phonons, which do not relate to particle resonances, are localized in the surrounding liquid medium and stem from coherent multiple scattering that becomes strong in the close-packing regime. Such rich phonon-matter interactions in nanostructures, being still unexplored, can open new opportunities in phononics.

Optically tunable surfaces with trapped particles in microcavities.

We introduce optically tunable surfaces based upon metallic gold nanoparticles trapped in open, water-filled gold cavities. The optical properties of the surfaces change dramatically with the presence and location of the particles inside the cavities. The precise position of the particles is shown to be controllable through optical forces exerted by external illumination, thus leading to all-optical tunability, whereby the optical response of the surfaces is tuned through externally applied light. We discuss the performance of the cavity-particle complex in detail and provide theoretical support for its application as a novel concept of a large-scale optically tunable system.

The "music" of core-shell spheres and hollow capsules: influence of the architecture on the mechanical properties at the nanoscale.

We report on the first measurement of elastic vibrational modes in core-shell spheres (silica-poly(methyl methacrylate), SiO2-PMMA) and corresponding spherical hollow capsules (PMMA) with different particle size and shell thickness using Brillouin light scattering, supported by numerical calculations. These localized modes allow access to the mechanical moduli down to a few tens of nanometers. We observe reduced mechanical strength of the porous silica core, and for the core-shell spheres a striking increase of the moduli in both the SiO2 core and the PMMA shell. The peculiar behavior of the vibrational modes in the hollow capsules is attributed to antagonistic dependence on overall size and layer thickness in agreement with theoretical predictions.

Plasmon guided modes in nanoparticle metamaterials.

Surface modes in nanostructured metallic metamaterial films are reported showing larger confinement than plasmons in metallic waveguides of similar dimensions, but in contrast to plasmons, the new modes have TE polarization. The metamaterial, formed by planar arrays of nearly-touching metallic nanoparticles, behaves as a high-index dielectric for the noted polarization, thus yielding well confined guided modes. Our results for silver particles in silica support a new paradigm for TE surface-wave guiding in unconnected nanostructured metallic systems complementary to TM plasmon waves in continuous metal surfaces.

Simultaneous occurrence of structure-directed and particle-resonance-induced phononic gaps in colloidal films.

We report on the observation of two hypersonic phononic gaps of different nature in three-dimensional colloidal films of nanospheres using Brillouin light scattering. One is a Bragg gap occurring at the edge of the first Brillouin zone along a high-symmetry crystal direction. The other is a hybridization gap in crystalline and amorphous films, originating from the interaction of the band of quadrupole particle eigenmodes with the acoustic effective-medium band, and its frequency position compares well with the computed lowest eigenfrequency. Structural disorder eliminates the Bragg gap, while the hybridization gap is robust.

Widening of phononic transmission gaps via Anderson localization.

We demonstrate the existence of strong Anderson localization in certain disordered phononic systems. As a result, the transmission coefficient of elastic waves through a slab of the material practically vanishes, whatever the angle of incidence, over a region of frequency much wider than the absolute frequency gap of the corresponding ordered system. The phenomenon can be of use in the design of phononic systems with very wide absolute transmission gaps.