The nanoscale manipulation of matter allows properties to be created in a material that would be difficult or even impossible to achieve in the bulk state. Progress towards such functional nanoscale architectures requires the development of methods to precisely locate nanoscale objects in three dimensions and for the formation of rigorous structure-function relationships across multiple size regimes (beginning from the nanoscale). Here, we use DNA as a programmable ligand to show that two- and three-dimensional mesoscale superlattice crystals with precisely engineered optical properties can be assembled from the bottom up. The superlattices can transition from exhibiting the properties of the constituent plasmonic nanoparticles to adopting the photonic properties defined by the mesoscale crystal (here a rhombic dodecahedron) by controlling the spacing between the gold nanoparticle building blocks. Furthermore, we develop a generally applicable theoretical framework that illustrates how crystal habit can be a design consideration for controlling far-field extinction and light confinement in plasmonic metamaterial superlattices.

Three-dimensional dielectric photonic crystals have well-established enhanced light-matter interactions via high Q factors. Their plasmonic counterparts based on arrays of nanoparticles, however, have not been experimentally well explored owing to a lack of available synthetic routes for preparing them. However, such structures should facilitate these interactions based on the small mode volumes associated with plasmonic polarization. Herein we report strong lightplasmon interactions within 3D plasmonic photonic crystals that have lattice constants and nanoparticle diameters that can be independently controlled in the deep subwavelength size regime by using a DNA-programmable assembly technique. The strong coupling within such crystals is probed with backscattering spectra, and the mode splitting (0.10 and 0.24 eV) is defined based on dispersion diagrams. Numerical simulations predict that the crystal photonic modes (Fabry-Perot modes) can be enhanced by coating the crystals with a silver layer, achieving moderate Q factors (∼10 2 ) over the visible and near-infrared spectrum.DNA-programmable assembly | 3D photonic crystals | plasmonics | deep subwavelength scale | strong coupling E nhancing light-matter interactions is essential in photonics, including areas such as nonlinear optics (1), quantum optics (2, 3), and high-Q lasing (4). In general, there are two ways of achieving this in optical cavities: (i) with long cavity lifetimes (high Q factors) and (ii) with strong photonic confinement (small mode volume, V) (2, 3). In particular, 3D dielectric photonic crystals, with symmetry-induced photonic band gaps (Bragg gaps), enhance light-matter interactions via high Q factors (4-6). However, the coupling strength between photons and electronic transitions within such systems is intrinsically weak owing to diffraction-limited photonic confinement (3, 7). Recently, it was suggested that a plasmonic counterpart of photonic crystals can prohibit light propagation and open a photonic band gap by strong coupling between surface plasmons and photonic modes (a polariton gap) if the crystal is in deep subwavelength size regime (8); these crystals have been referred to as polaritonic photonic crystals (PPCs) (9-12). This opens up the exciting possibility of combining plasmonics with 3D photonics in the strong coupling regime and optimizing the photonic crystals as small-mode-volume devices owing to the strong plasmonic mode confinement (13). However, such systems require control over the positioning of the plasmonic elements in the crystal on the nano-or deep subwavelength scale (8), and owing to this synthetic challenge such 3D PPCs have largely remained unexplored in the visible wavelength range.The recent discovery that DNA can be used to program the assembly of high-quality single crystals with well-defined crystal habits consisting of nanoparticles occupying sites in a preconceived lattice (14) opens up possibilities for fine tuning the interaction between light and highly organized collections of particles as a functi...

Capillary force-driven, large-area alignment of multi-segmented nanowires," ACM Nano, v. 8, no.2 (2014) pp. 1511-1516.

DNA-programmable assembly has been used to prepare superlattices composed of octahedral and spherical nanoparticles, respectively. These superlattices have the same body-centered cubic lattice symmetry and macroscopic rhombic dodecahedron crystal habit but tunable lattice parameters by virtue of the DNA length, allowing one to study and determine the effect of nanoscale structure and lattice parameter on the light-matter interactions in the superlattices. Backscattering measurements and finite-difference time-domain simulations have been used to characterize these two classes of superlattices. Superlattices composed of octahedral nanoparticles exhibit polarization-dependent backscattering but via a trend that is opposite to that observed in the polarization dependence for analogous superlattices composed of spherical nanoparticles. Electrodynamics simulations show that this polarization dependence is mainly due to the anisotropy of the nanoparticles and is observed only if the octahedral nanoparticles are well-aligned within the superlattices. Both plasmonic and photonic modes are identified in such structures, both of which can be tuned by controlling the size and shape of the nanoparticle building blocks, the lattice parameters, and the overall size of the three-dimensional superlattices (without changing habit).