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Jordan Austin-Frank Wilson

Publications and source records attributed to Jordan Austin-Frank Wilson.

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Correlated Plasmonic Excitation in Twisted Nematic Plasmonic Superlattices

Superlattices with twisted configurations, such as moire lattices, have recently been extensively exploited for their unique electronic, magnetic, and optical properties. One remarkable feature of nanoscale twisted superlattices is the distinct lattice symmetries and the continuous phase transitions between periodic or aperiodic phases, representing a unique opportunity to study many emerging physical phenomena. Here, we report a correlated light and matter interaction between the collective polarization effect of nematic plasmonic superstructures and the plasmonic excitation of individual constituent nanorods in reconfigurable twisted plasmonic superlattices. Using hybrid Fe3O4 and Au nanorods as building blocks, we assembled plasmonic nematic liquid crystals with unidirectionally aligned nanorods, which could be further assembled into moire plasmonic lattices through a vertical stacking assembly method. A twist angle dependent plasmonic excitation is recognized in the twisted bilayer of two plasmonic superlattices, featuring enhanced transverse and longitudinal plasmonic excitation at a twisting angle of 0 degree and 90 degree, respectively. Such correlated plasmonic excitation in twisted plasmonic superstructures is induced by the correlation between the collective polarization effect of the liquid crystal phases and the anisotropic plasmonic excitation of individual nanorods. The magnetic orientation control allows for precise alignment of hybrid Fe3O4 and Au nanorods in polymer substrates and enables the coding of nematic domains and plasmonic patterns in each sublattice. The correlated plasmonic excitation and light polarization create reconfigurable photonic moire superlattices with well-defined domain colors, feature sizes, periodicities, symmetries, and dimensions determined by twist angles and displacements in the twisted plasmonic lattices.

cond-mat.mtrl-sci

Shape-controlled growth of two-dimensional kagome-lattice colloidal crystals through nanoparticle capping

Organic capping ligands can selectively bind to crystal facets to modulate growth kinetics and are important in chemical synthesis of inorganic nanocrystals. Using the capping ligands for shape-controlled growth of colloidal crystals is challenging due to the size mismatch of molecules and nanoparticle building blocks. In existing synthetic pathways, colloidal crystal shapes are determined by their thermodynamically favored phases yet controlling their shapes independent of lattice symmetry is vital to study many solid-state properties. Here, we develop a nanoparticle capping strategy to control colloidal crystal shapes and structural heterogeneity. Au bipyramids were used as building blocks and assembled into rhombohedral colloidal crystals driven by DNA hybridization. In (111) planes of the crystals, bipyramids assembled into kagome lattices, featuring structure cavities organized in a hexagonal lattice. The rhombohedral crystals have truncated tetrahedral crystal habits, and the degree of truncation defines the exposed facets and crystal shapes. Our surface capping strategy is to introduce DNA-modified nanospheres as effective capping agents, which selectively register on the surface vacancies of the kagome facets and resemble the role of organic ligands in classic nanocrystal growth. Such selective capping is driven by maximizing DNA hybridization and leads to slower growth of the (111) kagome facets, changing the crystal shape from three-dimensional truncated tetrahedra to two-dimensional layered microplates with structural heterogeneity and shape anisotropy. This study underpins the importance of capping agents in colloidal crystal growth and inspires effective ways to control the growth kinetics and heterostructures of colloidal crystals.

cond-mat.soft