Optical transmission in triple-film hetero-opals

Angle-resolved transmission of s-polarized light in triple-film hetero-opals has been investigated in the spectral range including high-order photonic band gaps, and compared to the transmission of its constituent single-film opals. The interfaces do not destroy the predominantly ballistic light propagation over the studied frequency and angular ranges, but heterostructuring leads to a smoothed angular distribution of intensity of the transmitted light and to the reconstruction of the transmission minima dispersion. The interface transmission function has been extracted by comparing the transmission of the hetero-opal and its components in order to demonstrate the difference. This deviation from the superposition principle was provisionally assigned to light refraction and reflection at the photonic crystal interfaces and to the mismatch between mode group velocities in hetero-opal components

Order quantification of hexagonal periodic arrays fabricated by in situ solvent-assisted nanoimprint lithography of block copolymers

Directed self-assembly of block copolymer polystyrene-b-polyethylene oxide (PS-b-PEO) thin film was achieved by one-pot methodology of solvent vapour assisted nanoimprint lithography (SAIL).Comment: 12 pages, 4 figures, paper accepte

Long-Distance Indirect Excitation of Nanoplasmonic Resonances

In nanoscopic systems, size, geometry, and arrangement are the crucial determinants of the light-matter interaction and resulting nanoparticles excitation. At optical frequencies, one of the most prominent examples is the excitation of localized surface plasmon polaritons, where the electromagnetic radiation is coupled to the confined charge density oscillations. Here, we show that beyond direct near- and far-field excitation, a long-range, indirect mode of particle excitation is available in nanoplasmonic systems. In particular, in amorphous arrays of plasmonic nanodiscs we find strong collective and coherent influence on each particle from its entire active neighborhood. This dependency of the local field response on excitation conditions at distant areas brings exciting possibilities to engineer enhanced electromagnetic fields through controlled, spatially configured illumination

Facile electrochemical synthesis of Pd nanoparticles with enhanced electrocatalytic properties from surfactant-free electrolyte

Synthesis of low-dimensional metallic nanoparticles with a clean surface, high dispersibility, and enhanced atomic surface distribution is extremely important, as these factors strongly influence the electrocatalytic properties of the nanoparticles. In this study, the early stage electrochemical nucleation and growth of palladium nanoparticles (Pd NPs) under potentiostatic control has been investigated on a Au(111) textured substrate. The size distribution and structural characterization of the ex situ as-deposited Pd NPs by means of high-resolution field emission gun-scanning electron microscopy (FEG-SEM) at different stages combined with electrochemical measurements revealed that the cluster of nuclei grew independently through the reduction of metal ions. The electrodeposited Pd NPs were very pure, as confirmed by X-ray photoelectron spectroscopy (XPS), owing to the surfactant-free green electrodeposition process, and they exhibited a highly dispersed average particle size of 2–5 nm. The average nanoparticle size becomes smaller with higher overpotentials for the same deposition time. The synthesized Pd NPs demonstrated the largest specific surface area (four times that of commercial Pd−C) and electrocatalytic activity in ferrocyanide/ferricyanide redox and ethanol electrooxidation processes (35 times that of commercial Pd−C). This work represents an important step in achieving the fundamental understanding of nucleation and growth of nanoparticles correlating the electrocatalytic performances

Rechargeable Li-ion battery anode of indium oxide with visible to infra-red transparency

Unique bimodal distributions of single crystal epitaxially grown In2O3 nanodots on silicon are shown to have excellent IR transparency greater than 87% at 4 μm without sacrificing transparency in the visible region. These broadband antireflective nanodot dispersions are grown using a two-step metal deposition and oxidation by molecular beam epitaxy, and backscattered diffraction confirms a dominant (111) surface orientation. We detail the growth of a bimodal size distribution that facilitates good surface coverage (80%) while allowing a significant reduction in In2O3 refractive index. The (111) surface orientation of the nanodots, when fully ripened, allows minimum lattice mismatch strain between the In2O3 and the Si surface. This helps to circumvent potential interfacial weakening caused by volume contraction due to electrochemical reduction to lithium, or expansion during lithiation. Cycling under potentiodynamic conditions shows that the transparent anode of nanodots reversibly alloys lithium with good Coulombic efficiency, buffered by co-insertion into the silicon substrate. These properties could potentially lead to further development of similarly controlled dispersions of a range of other active materials to give transparent battery electrodes or materials capable of non-destructive in-situ spectroscopic characterization during charging and discharging

Plasmonic Nanowire Antennas: Experiment, Simulation, and Theory

Recent advances in nanolithography have allowed shifting of the resonance frequency of antennas into the optical and visible wavelength range with potential applications, for example, in single molecule spectroscopy by fluorescence and directionality enhancement of molecules. Despite such great promise, the analytical means to describe the properties of optical antennas is still lacking. As the phase velocity of currents at optical frequencies in metals is much below the speed of light, standard radio frequency (RF) antenna theory does not apply directly. For the fundamental linear wire antenna, we present an analytical description that overcomes this shortage and reveals profound differences between RF and plasmonic antennas. It is' fully supported by apertureless scanning near-field optical microscope measurements and finite-difference time-domain simulations. This theory is a starting point for the development of analytical models of more complex antenna structures

Quantitative and Direct Near-Field Analysis of Plasmonic-Induced Transparency and the Observation of a Plasmonic Breathing Mode

We investigated experimentally and numerically in the optical near-field a plasmonic model system similar to a dolmen-type structure for phenomena such as plasmon-induced transparency. Through engineering of coupling strength, structure orientation, and incident angle and phase of the excitation source it was possible to control near-field excitation of the dark modes. We showed that quantitative analysis of near-field amplitude and excitation strength provided essential information that allowed identifying the interaction between the bright and the dark mode and how it causes the formation of plasmon-induced transparency features and a Fano resonance. In addition, we introduced a mechanism to excite field distributions in plasmonic structures that cannot be accessed directly using far-field illumination and demonstrated the excitation of a dark mode akin to a symmetry-forbidden plasmonic breathing mode using a linearly polarized far-field source

Near-Field Dynamics of Optical Yagi-Uda Nanoantennas

We present near-field measurements of optical Yagi-Uda nanoantennas that are used in receiving mode. The eigenmode imaging of amplitude and phase by apertureless scanning near-field optical microscopy allows us to investigate the dynamics of the local out-of-plane electric field components and to visualize the temporal evolution of this time-harmonic reception process. The antenna directionality manifests itself by the dependence of the local field enhancement at the feed element on the illumination direction. Simulations taking into account the substrate confirm our observation of the directionality. Our work demonstrates the possibility to characterize multielement nanoantennas by electromagnetic antenna near-field scanners