Revealing the Absence of Carbon in Aprotic Li–CO2 Batteries: A Mechanism Study Toward CO2 Reduction Under a Pure CO2 Environment

While attention is focused on Li–CO2 batteries due to their high energy density and ability to utilize carbon, their detailed cathodic reaction mechanism remains unclear. Thus far, the recognized reaction...

Cylindrical model of electrochromic colouration of hydrated vanadium pentoxide thin films with point contacts

This article analyses experiments on the kinetics of the internal electrochromism of thin (micron) films of hydrated vanadium pentoxide xerogel with point contacts. It describes a cylindrical model of electrochromic colouration, which was used to evaluate the concentration of the colour centres in the initial film and after additional hydrogenation of this film by plasmaimmersion ion implantation.When we compared the calculated values of the concentration of colour centres with the equilibrium concentration of protons in the xerogel, we saw that the mobility of the protons migrating from the depth of the film to the cathode region, which are involved in the electrochemical reaction, was not a determinant of the electrochromism kinetics.The rate of electrochromic colouration could be increased by the formation of layered film structures based on hydrated vanadium pentoxide, which have increased overall electron conductivity and, as a consequence, low faradaic resistance of the electrochromic cathodic reaction.

Aizoon Extract As a Novel Eco-friendly Corrosion Inhibitor For Stainless Steel430 in HCl Solution

Aizoon extract used as anti-corrosion for stainless steel430 (SS430) in 2M hydrochloric acid solution. The mass reduction, electrochemical impedance, and potentiodynamic polarization were carried out to demonstrate the performance of Aizoon extract as corrosion resistance for SS430. Polarization revealed that the Aizoon extract is mixed type inhibitor with superiority to inhibiting the cathodic reaction. The inhibition percentage reaches 93% at 300 ppm extract. Adsorption of the extract on SS430 surface is regular with Langmuir adsorption model. Thermodynamic factors for adsorption and activation processes for SS430 dissolution were estimated and discussed. Furthermore, the SS430 surface is characterized using different techniques. The surface morphology of SS430 was tested utilizing several techniques. The experimental data were supported by the theoretical data.

CORROSION INHIBITION OF CARBON STEEL IN HYDROCHLORIC ACID

The corrosion of carbon steel in 0.3 and 3% mass hydrochloric acid containing the concentration range 50-800 ppm of Thiourea (Th), Quinoline (Q), Dliethylamine (DEA) and Pyridine (P) were investigated using electrochemical methods. The investigation aims to mention the best organic inhibitor among several compounds to be used in synergic inhibitors. The inhibition efficiencies of thiourea and quinoline are better than pyridine and diethylamine in 0.3 mass% HCl. Thiourea is better than quinoline in 3 mass% HCl and its inhibition efficiency is 83.7%. Generally, the corrosion rate decreases with increasing inhibitors concentration. Diethylamine and pyridine are not effective. The polarization curves indicate that the used inhibitors influenced the cathodic reaction more than the anodic reaction and they are considered as a mixed type inhibitors

Electrophotocatalytic diamination of vicinal C–H bonds

The conversion of unactivated carbon-hydrogen (C–H) bonds to carbon–nitrogen (C–N) bonds is a highly valued transformation. Existing strategies typically accomplish such reactions at only a single C–H site because the first derivatization diminishes the reactivity of surrounding C–H bonds. Here, we show that alkylated arenes can undergo vicinal C–H diamination reactions to form 1,2-diamine derivatives through an electrophotocatalytic strategy, using acetonitrile as both solvent and nitrogen source. The reaction is catalyzed by a trisaminocyclopropenium (TAC) ion, which undergoes anodic oxidation to furnish a stable radical dication while the cathodic reaction reduces protons to molecular hydrogen. Irradiation of the TAC radical dication (wavelength of maximum absorption of 450 to 550 nanometers) with a white-light compact fluorescent light generates a strongly oxidizing photoexcited intermediate. Depending on the electrolyte used, either 3,4-dihydroimidazole or aziridine products are obtained.

Cathodic electroorganic reaction on silicon oxide dielectric electrode

The faradaic reaction at the insulator is counterintuitive. For this reason, electroorganic reactions at the dielectric layer have been scarcely investigated despite their interesting aspects and opportunities. In particular, the cathodic reaction at a silicon oxide surface under a negative potential bias remains unexplored. In this study, we utilize defective 200-nm-thick n+-Si/SiO2 as a dielectric electrode for electrolysis in an H-type divided cell to demonstrate the cathodic electroorganic reaction of anthracene and its derivatives. Intriguingly, the oxidized products are generated at the cathode. The experiments under various conditions provide consistent evidence supporting that the electrochemically generated hydrogen species, supposedly the hydrogen atom, is responsible for this phenomenon. The electrogenerated hydrogen species at the dielectric layer suggests a synthetic strategy for organic molecules.

Galvanic Corrosion Due to a Heterogeneous Sulfate Reducing Bacteria Biofilm

In this work, the galvanic corrosion behavior of sulfate reducing Desulfotomaculum nigrificans biofilm-covered and uncovered carbon steel was investigated using various electrochemical measurements. The results showed that the bare specimen in the abiotic solution functions as the anode; whereas the biofilm-covered specimen in the SRB-containing solution functions as the cathode after two electrodes being coupled. The anodic reaction of specimen in the biotic solution containing SRB was inhibited; whereas the cathodic reaction was considerably promoted after coupling. Hence, localized corrosion of specimen in the abiotic solution was observed due to the galvanic corrosion effect. SRB could still accelerate steel corrosion even after coupling, but the results indicate that the contribution of SRB to steel corrosion decreased. The localized corrosion of steel in the SRB-containing environments not only involved the SRB biofilm, but also a galvanic corrosion effect. The flow of electrons from the anodic dissolution of Fe in the abiotic solution to the SRB cells of cathodic area decreased the acceptance capacity of electrons by SRB from steel beneath biofilm. As a result, the steel corrosion beneath SRB biofilm decreased after coupling.