ZnO@Bi5O7I Heterojunction Derived from ZIF-8@BiOI for Enhanced Photocatalytic Activity under Visible Light

In the study, ZIF-8@BIOI composites were synthesized by the hydrothermal method and then calcined to acquire the ZnO@Bi5O7I composite as a novel composite for the photocatalytic deterioration of the antibiotic tetracycline (TC). The prepared ZnO@Bi5O7I composites were physically and chemically characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), Brunauer–Emmet–Teller (BET) surface area, UV–Vis diffuse reflectance spectroscopy (DRS), emission fluorescence spectra, transient photocurrent response, electrochemical impedance spectra and Mott–Schottky. Among the composites formed an n–n heterojunction, which increased the separation efficiency of electrons and holes and the efficiency of charge transfer. After the photocatalytic degradation test of TC, it showed that ZnO@Bi5O7I (2:1) had the best photodegradation effect with an 86.2% removal rate, which provides a new approach to the treatment of antibiotics such as TC in wastewater.

Analysis of MEA’s durability under Accelerated Stress Tests that mimic realistic automotive operations

This work aims at studying MEA’s ageing under single operational “mode” accelerated stress tests (AST), that were specifically designed to replicate under hydrogen/air feeding the main stressors of realistic operations in the automotive sector. A methodology for developing AST is here presented and preliminary results about the activity included. In particular, low power and high power functioning have been mimicked in a Zero-Gradient hardware, which allows a reliable materials comparison. Quantities, measurable in-situ and operando, have been tracked during ageing, like cell power, polarization curves, Pt active area, oxygen mass transport resistance, Electrochemical Impedance Spectra. The final objective is to clarify the underlying ageing mechanisms and assess the contribution of each specific operation to the MEA lifetime, focusing in particular on the cathode catalyst layer durability. Moreover, the rate of voltage loss for the new ASTs has been successfully correlated to the degradation observed under a complete driving cycle protocol.

Vanadium and Tannic Acid-Based Composite Conversion Coating for 6063 Aluminum Alloy

In this study, a vanadium (V) and tannic acid-based composite conversion coating (VTACC) was prepared on 6063 aluminum alloy (AA6063) to increase its corrosion resistance. The surface morphology and compositions of the VTACCs were characterized using scanning electron microscopy (SEM), energy dispersive spectrometry (EDS), and X-ray photoelectron spectroscopy (XPS). The corrosion resistance of the coatings was investigated by linear polarization and electrochemical impedance spectra (EIS). The self-healing ability of the coating was detected by SEM, EDS, and scanning vibrating electrode technique (SVET) measurements. The coating mainly consisted of metal oxides, including Al2O3, VO2, V2O3, and V2O5, and metal organic complexes (Al and V-complexes). The electrochemical measurement results indicated that the best corrosion resistance of VTACC was acquired when the treatment time was 12 min. Furthermore, because a new coating with vanadium rich oxide was developed on the scratch area, artificial scratch VTACC surfaces were repaired after several days of immersion in 3.5-wt% NaCl solution.

Electrochemical behaviors and discharge performance of Mg-Sn binary alloys as anodes for Mg-air batteries

In this work, the self-corrosion and discharge performance of the as-cast Mg-xSn (x=1, 5, 9 wt.%) anodes for primary Mg-air batteries were studied through microstructure characterization, electrochemical testing and discharge experiments. With the increase of Sn content, the volume fraction of the Mg2Sn phase increases, promoting dendrite refining. According to the electrochemical test, the Mg-1Sn anode shows a higher open circuit potential, resulting in a stronger electrochemical activity. The polarization curve and electrochemical impedance spectra show the corrosion resistance order as Mg-1Sn>Mg-5Sn>Mg-9Sn. In the discharge measurement, the Mg-1Sn anode achieves the best average discharge voltage, anode efficiency, specific capacity, and energy density under all current densities tested. At 10 mA cm-2, the energy density of Mg-1Sn is 1239.621 mWh g-1, which is higher than the Mg-5Sn anode and Mg-9Sn anode, 37% and 25%, respectively. The optimal discharge performance of the Mg-1Sn anode is mainly attributed to the high electrochemical activity and the micron-sized Mg2Sn phase dispersed in the matrix, which facilitates more uniform dissolution.

Experimental Study on the Corrosion of Carbon Steel and Aluminum Alloy in Firefighting Protein Foam Concentrates

The corrosion of mild steel and Al alloy in Fomtec P 6% and 6% P Profoam 806 protein-based foam concentrates was investigated. Weight-loss data for steel showed corrosion penetration of 0.745 mipy in Fomtec and 2.269 mipy in Profoam, whereas for Al alloy the penetration levels were 0.474 and 1.093 mipy, respectively. Scanning electron microscopy and energy dispersive X-ray spectroscopy allowed characterization of the metallic surface covered or free from corrosion products. Values of corrosion potential, corrosion current density and corrosion penetration were calculated by using potentiodynamic polarization curves. Electrochemical impedance spectra illustrated the change in polarization resistance during anodic polarization. Data obtained by accelerated electrochemical methods confirm the greater aggressiveness of the Profoam concentrate compared to Fomtec concentrate.

One-Step Electrodeposition of Superhydrophobic Coating on 316L Stainless Steel

Superhydrophobic coatings were fabricated through a one-step electrochemical process onto the surface of 316L stainless steel samples. The presence of hierarchical structures at micro/nanoscale and manganese stearate into the coatings gave superhydrophobicity to the coating, with contact angle of ~160°, and self-cleaning ability. Corrosion resistance of 316L samples was also assessed also after the electrodeposition process through Electrochemical Impedance Spectra recorded in an aqueous solution mimicking seawater condition.

Creating and Preserving Nanoparticles during Co-Sintering of Solid Oxide Electrodes and Its Impact on Electrocatalytic Activity

A novel processing method that creates and preserves ceramic nanoparticles in solid oxide electrodes during co-sintering at traditional sintering temperatures is introduced. Specifically, carbon templated samarium-doped ceria nanoparticles (nSDC) were successfully integrated with commercial lanthanum strontium cobalt ferrite (LSCF) and commercial SDC powders, producing LSCF-SDC-nSDC cathodes upon processing. The effect of nSDC concentration on cathode electrocatalytic activity was investigated at low operational temperatures, 600 °C–700 °C, with symmetrical cells. Low nSDC loadings, ≤5 wt% nSDC, significantly decreased cell polarization resistance whereas higher loadings increased it. The best electrochemical performance was achieved with 5 wt% nSDC, lowering the polarization resistance by 41% at 600 °C. Fuel cell tests demonstrate that adding 5 wt% nSDC increased the maximum fuel cell power density by 38%. Electrochemical impedance spectra showed substantial improvements in both fuel cell polarization resistance and ohmic resistance, indicating that nSDC increased the electrocatalytically active area of the cathode. This work demonstrates a simple, novel method for effectively increasing electrocatalytic activity of solid oxide electrodes at low operational temperatures.