Unveiling Local Optical Properties Using Nanoimaging Phase Mapping in High-Index Topological Insulator BiSe Resonant Nanostructures.

Topological insulators are materials characterized by an insulating bulk and high mobility topologically protected surface states, making them promising candidates for future optoelectronic and quantum devices. Although their electronic properties have been extensively studied, their mid-infrared (MIR) properties and prospective photonic capabilities have not been fully uncovered. Here, we use a combination of far-field and near-field nanoscale imaging and spectroscopy to study chemical vapor deposition-grown BiSe nanobeams (NBs).

Salt-induced stability and modified interfacial energetics in self-faceting emulsion droplets.

Hypothesis: The counterintuitive temperature-controlled self-faceting of water-suspended, surfactant-stabilized, liquid oil droplets provides new opportunities in engineering of smart liquids, the properties of which are controllable by external stimuli. However, many emulsions exhibiting self-faceting phenomena have limited stability due to surfactant precipitation. The emulsions' stability may be enhanced, and their inter-droplet electrostatic repulsion tuned, through controlled charge screening driven by varying-concentration added salts.

Chemical Vapor Deposition of Spherical Amorphous Selenium Mie Resonators for Infrared Meta-Optics.

Applying direct growth and deposition of optical surfaces holds great promise for the advancement of future nanophotonic technologies. Here, we report on a chemical vapor deposition (CVD) technique for depositing amorphous selenium (a-Se) spheres by desorption of selenium from BiSe and re-adsorption on the substrate. We utilize this process to grow scalable, large area Se spheres on several substrates and characterize their Mie-resonant response in the mid-infrared (MIR) spectral range.

Denser fluids of charge-stabilized colloids form denser sediments.

Granular matter, where solid-like elasticity emerges in the absence of crystalline order, has been actively studied over the last few decades, targeting fundamental physical understanding of granular packings and glasses, abundant in everyday life and technology. We employ charge-stabilized sub-micron particles in a solvent, known as colloids, to form granular packings through a well-controlled process, where initially homogeneous and thermodynamically equilibrated colloidal fluids form solid sediments, when subjected to an effective gravity in a centrifuge. We demonstrate that particles' volume fraction φj in these sediments increases linearly with that in the initial fluid φ0, setting an upper limit φRCP≈ 0.