Light Detection and Ranging (LiDAR) is a primary sensor for autonomous vehicles to recognize surroundings. It detects near-infrared (NIR) light pulses, typically at 905nm, which is emitted and reflected by surrounding objects. Here, the fact of the matter is that conventional black or dark-tone cars with extremely low NIR reflection are hard to be detected by LiDAR and endanger the future highway. In this work, we propose to use platelet-shaped effect pigments with visible absorption and NIR reflectivity. Copper(Ⅱ) oxide and Silicon dioxide multilayer are theoretically investigated with different numbers of layers and thicknesses. The optimized structures appear various dark-tone colors with high NIR-reflectivity over 90%.

Ceria (CeO2) possesses a distinctive redox property due to a reversible conversion to its nonstoichiometric oxide and has been considered as a promising catalyst in the oxidative coupling of methane. Since a heterogeneously catalytic process usually takes place only on the surface of catalysts, it is reasonably expected that the performance of a catalyst, such as CeO2, highly relies on its size- and shape-dependent surface structure. We report our recent progress in achieving exclusive crystal facet-terminated CeO2 nanocrystals using a shape-controlled synthesis protocol in a one-pot colloidal system. We modified a two-phase solvothermal approach to fabricate cubic and truncated octahedral CeO2 nanocrystals with a size-control. During the two-phase solvothermal process, we propose that the Ce-precursors transfer from the aqueous layer to the interface of the organic phase, promoted by the capping ligands (as known as phase-transfer catalysts), for the oxidation and nucleation, and subsequently form CeO2 nanocrystals in the organic layer. As different capping ligands favor binding on diverse crystal facets, tuning the composition of the capping ligand with a precise control could generate nanocrystals that are dominated by a single type of facets with a relatively narrow size distribution.

Metallic palladium (Pd) is used for hydrogen storage and detection. Fabrication of a nanoporous (NP) Pd structure can increase the specific surface area leading to a significant improvement in the sensitivity. In our previous study, we succeeded in forming a NP-Pd film by dealloying an Al-Pd alloy film using citric acid as a chelating agent. This method was environmentally friendly but had a long reaction time and a considerable amount of Al remained after dealloying; hence, the Pd purity was reduced. In this study, we succeeded in forming a higher purity NP-Pd film faster by dealloying the nitrogen-containing Al-Pd (Al-Pd-N) film using ethylene-diamine-tetraacetic-acid (EDTA) as a chelating material.

In a deep geological repository (DGR) scenario, uranium oxidized in aqueous systems will be stabilized as UO22+ (hexavalent uranium), as a consequence of tetravalent uranium oxidation by radiolytic byproducts. Uranyl cationic species (UO22+) in different speciation forms are expected to be found at the whole pH range conditions. The importance of UO22+ lies in its potential incorporation of trace radioelements onto secondary uranyl phases. In view of the difficulty of U chemistry in natural groundwater, it is necessary to improve speciation assessment techniques so as to understand chemical processes. Raman spectroscopy has been shown as a powerful tool to analyze the speciation of various actinyl (UO22+,NpO2+ and PuO22+) and to determine the distribution of those elements which are more likely to be stable in a near-field groundwater environment. Therefore, the aim of this work is to follow UO22+ changes as a consequence of γ radiation in aqueous media under DGR conditions, and to understand the behavior of UO22+ as a function of aqueous media, which help to understand and predict the potential precipitation of the solid phases formed. In this work, the use of Raman spectroscopy adapted to the empirical analysis of different nuclear applications for initial uranium concentrations 0.04M at ambient atmosphere is shown, i.e. as monitoring tool for UO22+ precipitation as a function of pH, studying UO2(NO3)2·6H2O stability in aqueous solutions representative of groundwater, in particular at ionic strength I = 0.02 – 0.4 M and pH from 7 to 13.2; and to evaluate the effect of γ radiation fields. At 10−4-10-3 M of radiolytically formed H2O2 concentration, the amount of uranium in solution decreased, as a results of secondary phases precipitation. The results obtained will be useful to the performance assessment studies of the Spent Nuclear Fuel (SNF) stored in DGRs. The work performed provides a partial picture of secondary phase formations, as a result of corrosion of SNF in a DGR.

Ion beam analyses were completed on single crystal LiD (lithium hydride with deuterium on the hydrogen sites) to determine products of hydrolysis with decarbonated H2O (with protium-hydrogen) in an inert gas. Rutherford backscattering spectrometry showed movement of oxygen into the bulk of LiD samples. Hydrolysis rates for the single crystal LiD showed relatively slow initial growth of an oxygen-containing layer. Final growth rates varied widely with H2O level, from 1010 to 1015 (atoms/cm2)/min. at 5.6 and 28 mmol/min. H2O respectively. Simulations of spectra show the hydrolysis product to be LiOH. Elastic recoil detection identifies the hydrogen in the hydroxide layer upon dosing with H2O (with natural, protiated hydrogen) as primarily protium. Micrographs showed island growth occurring initially, with convergence to a full-coverage hydrolysis layer.

Crack initiation in zirconium alloys is an important issue for the safety of water-cooled fission reactors. Zirconium hydrides that precipitate in service are potential crack nucleation sites. In this work, the deformation and cracking of zirconium hydrides was studied during room temperature deformation of a Zircaloy-4 tensile sample up to fracture. The sample contained a hydrogen concentration of 100 ± 20 ppm. The main aims of this study were to better understand the mechanisms behind the hydride fracture in a polycrystalline matrix, and to identify at which point in the deformation of the Zr matrix the first hydrides break. Cracks thus nucleated may coalesce and propagate through the hydrided Zr-alloy. Scanning electron microscopy (SEM) images of a number of hydrides, both intergranular and intragranular, were taken at discrete increments of deformation during an interrupted tensile test. The results show that cracks in hydrides tend to always occur normal to the applied load, signalling the importance of the external stress. However, evidence is also provided to support the hypothesis that internal stresses generated by microstructural constraints may lead to the fracture of some intergranular hydrides.

Investigations of the crystallization of aluminosilicate phases within Hanford nuclear waste glasses typically involve subjecting samples to the canister centerline cooling (CCC) schedule. This cooling schedule is representative of the slowest cooling thermal profile which these glasses will experience after the glass is poured into the high level waste (HLW) container. However, few investigations have observed how the crystallization behavior changes by varying the heat treatment schedule. In the present study, three Hanford HLW glasses are subjected to CCC and isothermal heat treatments (IHT) to better understand the evolution of phases and the chemical partitioning due to temperature schedule. Samples were characterized using electron probe microanalysis, X-ray diffraction, micro X-ray fluorescence, and micro X-ray absorption spectroscopy. From IHT, eucryptite and apatite phases were observed which were not observed during CCC. Spatially-resolved measurements demonstrated that the oxidation state of the iron was similar among glass and crystal, and we suggest a mechanism to describe the compositional fluctuations near the crystal-glass interface which influence crystallization.

The present research was aimed to study the degradation of 2-Chlorophenol through the use of bismuth molybdate (γ-Bi2MoO6) structures supported on graphene oxide (GO) which is intended to control the recombination of charge carriers. γ-Bi2MoO6/GO systems were doped with nitrogen via chemical reaction, to reduce their energy gap, improving their photocatalytic activity. Structural and physicochemical characterization of the resulting catalysts were performed using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), and UV-Vis. The obtained compounds show good photo catalytic performance when using visible energy to degrade 2-Chlorophenol, obtaining 80% of degradation in 65 min.