ABSTRACT
We study the optical response of a metamaterial surface created by a lattice of split-ring resonators covered with a nematic liquid crystal and demonstrate millisecond timescale switching between electric and magnetic resonances of the metasurface. This is achieved due to a high sensitivity of liquid-crystal molecular reorientation to the symmetry of the metasurface as well as to the presence of a bias electric field. Our experiments are complemented by numerical simulations of the liquid-crystal reorientation.
Subject(s)
Liquid Crystals/chemistry , Liquid Crystals/radiation effects , Manufactured Materials , Models, Chemical , Refractometry/instrumentation , Computer Simulation , Computer-Aided Design , Electromagnetic Fields , Equipment Design , Equipment Failure Analysis , Light , Models, Theoretical , Molecular Conformation/radiation effectsABSTRACT
Locally probing chemical reactions or catalytic processes on surfaces under realistic reaction conditions has remained one of the main challenges in materials science and heterogeneous catalysis. Where conventional surface interrogation techniques usually require high-vacuum conditions or ensemble average measurements, plasmonic nanoparticles excel in extreme light focusing and can produce highly confined electromagnetic fields in subwavelength volumes without the need for complex near-field microscopes. Here, we demonstrate an all-optical probing technique based on plasmonic smart dust for monitoring local chemical reactions in real time. The silica shell-isolated gold nanoparticles that form the smart dust can work as strong light concentrators and optically report subtle environmental changes at their pinning sites on the probed surface during reaction processes. As a model system, we investigate the hydrogen dissociation and subsequent uptake trajectory in palladium with both "dust-on-film" and "film-on-dust" platforms. Using time-resolved single particle measurements, we demonstrate that our technique can in situ encode chemical reaction information as optical signals for a variety of surface morphologies. The presented technique offers a unique scheme for real-time, label-free, and high-resolution probing of local reaction kinetics in a plethora of important chemical reactions on surfaces, paving the way toward the development of inexpensive and high-output reaction sensors for real-world applications.
Subject(s)
Chemical Phenomena , Gold/chemistry , Hydrogen/chemistry , Silicon Dioxide/chemistry , Catalysis , Kinetics , MicroscopyABSTRACT
We theoretically calculate the electromagnetic response of metallic rod dimers for the arbitrary planar arrangement of rods in the dimer. It is shown that dimers without an in-plane symmetry axis exhibit elliptical dichroism and act as "atoms" in planar chiral metamaterials. Because of a very simple geometry of the rod dimer, such planar metamaterials are much easier to fabricate than conventional split-ring or gammadion-type structures and lend themselves to a simple analytical treatment based on a coupled dipole model. Dependencies of the metamaterial's directional asymmetry on the dimer's geometry are established analytically and confirmed in numerical simulations.
