We investigate the origin of satellite features that appear in the high-resolution x-ray absorption spectra measured at the uranium M4 edge in compounds where the uranium atoms are in the U6+ oxidation state. We employ a material-specific Anderson impurity model derived from the electronic structure obtained by the density-functional theory.

A brief review of the status of our understanding of the occupation of the Pu 5f states is provided herein, with an emphasis upon experimental measurements.

It is of great significance to understand and monitor the condition of the commercial batteries in EVs/HEVs and stationary applications under their real working situations. Electrochemical impedance spectroscopy (EIS) has been proved to be a powerful technique for investigating the kinetics and redox reactions at the interfaces, as well as the diffusion behavior in the bulks of every electrochemical systems. Focusing on tracing the temperature of the commercial batteries during the EIS tests at different stages in a well-designed four-week driving simulation, the value of temperature profile during the EIS test as an enhanced indicator to help analyzing the formation of the passivation layers, electrolyte impedance development as well as lithium plating on the anode through EIS analysis have been found.

Stimuli-responsive materials with controlled reversible wettability find diverse application as self-cleaning surfaces, tunable optical lenses and microfluidic devices. We report on an electrochemical approach for dynamic control over the wetting properties of additive-free Cu/CuxO core-shell dendritic structures. By varying the oxidation state of the oxide shell phase, the entire wettability range spanning superhydrophobicity (contact angle > 150°) to superhydrophilicity (contact angle < 10°) can be precisely adjusted in-situ. During the wetting transitions, the surface transforms from a low adhesive rolling state (lotus effect) to high adhesive pinning state (petal effect), and eventually to superhydrophilic state with a water-absorbing ability (fish scale wetting). The wetting alteration is reversible via air-drying at room temperature or mild heat drying at 100°C. The reversibly redox-driven wettability switching is demonstrated for controllable oil-water separation with efficiency higher than 98 percent.

Overpotential losses on cathode during oxygen reduction reaction (ORR) causes serious performance depletion in microbial fuel cells (MFCs). High cost of existing platinum based noble catalysts is one of the main reason for growing interest in the research of low cost sustainable cathode catalysts to improve ORR in order to enhance power generation from MFCs. The present study demonstrates application of low-cost bimetallic ferrite, Co0.5Zn0.5Fe2O4, as a cathode catalyst in MFC. The electrochemical tests of cathode having this catalyst revealed an excellent cathodic current response of 25.76 mA with less charge transfer resistance of 0.7 mΩ, showing remarkable catalytic activity. The MFC using this catalyst on cathode could generate a power density of 172.1 ± 5.2 mW/m2, which was found to be about 10 times higher than the power density of 15.2 ± 1.3 mW/m2 obtained from a MFC using only acetelyne black (AB) on cathode and noted even higher than the power density produced by MFC with Pt/C cathode (151.3 ± 2.8 mW/m2). In addition, the wastewater treatment in terms of chemical oxygen demand (COD) removal efficiency of MFC with Co0.5Zn0.5Fe2O4 on cathode was found to be better (87 %) among the tested MFCs. Hence, the results obtained from this study illustrates the applicability of Co0.5Zn0.5Fe2O4 as an excellent and suitable cathode catalyst for scaling up of MFCs.

Anti-organic fouling performance of titanium dioxide (TiO2) can be enhanced by extending its light absorption and photocatalytic capability from ultra-violet to the visible range through hydrogenation. In this work, we aim at studying the impact of hydrogenation on the performance of both electron beam-deposited TiO2 thin films and hydrothermally grown TiO2 nanostructures on titanium substrates. Hydrogenation of these TiO2-deposited titanium substrates (TiO2/Ti) are achieved in relatively low-temperature low-pressure chemical vapor deposition chamber without any noble diatomic hydrogen dissociation catalyst, such as platinum. Our study shows that these hydrogenated TiO2/Ti have better light absorption ability and the titanium substrate itself serves as the active catalyst for hydrogen dissociation and diffusion. By applying hydrogenation to the TiO2 nanostructures, we can enhance photocatalytic performance by 50% through methylene blue degradation experiments. We have also evaluated the effect of hydrogenation on carrier density and mobility in TiO2/Ti. We recommend the hydrogenation of hydrothermally grown TiO2 nanostructure on titanium substrates for scalable photocatalytic applications.