Search Results (7)

Different classes of solid electrolytes for all-solid-state batteries (ASSB) are currently being investigated, with each of them suitable for a different ASSB concept. Their combination in hybrid battery cells enables the use of their individual benefits while mitigating their disadvantages. The cubic stuffed garnet Li₇La₃Zr₂O₁₂ (LLZO), for example, is stable in contact with metallic lithium but has only moderate ionic conductivity, whereas the thiophosphate Li₁₀SnP₂S₁₂ (LSPS) is processable using conventional battery manufacturing technologies and has an excellent lithium-ion conductivity but an inferior electrochemical stability. In this work, we, therefore, present a layered hybrid all-solid-state full-cell concept that accommodates a lithium metal anode, a LiNi_0.8Co_0.1Mn_0.1O₂-based composite cathode with an LSPS catholyte (LSPS/NCM811) and a sintered monolithic LLZO separator. The electrochemical stability of LLZO and LSPS at cathodic potentials (up to 4.2 V) was investigated via cyclic voltammetry in test cells, as well as by cycling half cells with LSPS or a mixed LSPS/LLZO catholyte. Furthermore, the pressure-dependency of the galvanostatic cycling of a Li | LLZO | LSPS/NCM811 full cell was investigated, as well as the according effect of the Li | LLZO interface in symmetric test cells. An operation pressure of 12.5 MPa was identified as the optimal value, which assures both sufficient inter-layer contact and impeded lithium penetration through the separator and cell short-circuiting. Full article

One of the main sources of non-ferrous and precious metals is sulfide ores. This paper presents a review of the existing literature on the electrochemical properties of some of the most common industrial sulfides, such as pentlandite, chalcopyrite, sphalerite, galena, pyrrhotite, pyrite, etc. The study results of the surface redox transformations of minerals, galvanic effect, cathodic oxygen reduction reaction on the surface of sulfides are presented. The electrochemical properties of sulfide minerals are manifested both in the industrial processes of flotation and hydrometallurgy and in the natural geological setting or during the storage of sulfide-containing mining, mineral processing, and metallurgical industry waste. Full article

Removing CO₂ from natural gas or biogas in the presence of H₂S is technically challenging and expensive as it often requires separation of both acid gases from the gas, typically using an aqueous amine solution, followed by separation of CO₂ from H₂S and conversion of H₂S into solid S. In this work, the proof of concept of electrochemical, instead of thermal, regeneration of an aqueous amine solution is developed. This invention might be a very promising technology and has several advantages. It has H₂S versus CO₂ selectivity of 100%, can directly convert H₂S into S and H₂, and is economically competitive with CO₂ desorption energy around 100 kJmol⁻¹ and H₂S conversion around 200 kJmol⁻¹. If renewable energy is used for electrochemical regeneration, CO₂ emissions due to the CO₂ capture process can be significantly reduced. Full article

During Bayer alumina production with high-sulfur bauxite, the sulfide ions in the sodium aluminate solution caused serious corrosion to Q235 steel, which is the material of the tank equipment. This study investigates the effect of corrosion time on Q235 steel synergistic corrosion in sodium aluminate solution using the weight-loss method and electrochemical measurements. The results indicate that the corrosion rate decreases sharply, the rate equation satisfies the mathematical model of power function at the initial stage of corrosion, and the transformation of unstable iron sulfide to stable iron oxide at the later stage results in the decrease in sulfur content in the corrosion products and surface pseudo-passivation. There are two main types of corrosion products, as follows: one is the octahedral crystal particle, which is composed of Fe₂O₃, Fe₃O₄, Al₂O₃ and NaFeO₂, and the other is the interlayer corrosion between the surface layer and the matrix, which is composed of FeS, FeS₂ and MnS₂. At day 3, the dynamics of the Q235 steel electrode is controlled by charge transfer and ion diffusion. However, at other times the dynamics are mainly controlled by charge transfer. Full article

Efficient extraction of Ni, Co, Cu, and Mn from low-grade and refractory ores is a common technical challenge. The present study proposes an Acidithiobacillus ferrooxidans-coupled leaching of Ni, Cu, Co, and Mn from oceanic polymetallic nodules and low-grade nickel sulfide ore, and focuses on the electrochemical behavior of the ores in simulated bio-leaching solutions. In the dissolution of polymetallic nodules, A. ferrooxidans facilitates the diffusion of H⁺ and accelerates electron transfer, producing a decrease in charge transfer resistance and promoting the Mn(IV)-preceding reaction. The use of A. ferrooxidans is beneficial for lower impedance of sulfur-nickel ore, faster diffusion rate of product layer, and better transformation of the Fe³⁺/Fe²⁺ couple and S⁰/S²⁻ couple. A. ferrooxidans increases the potential difference between the nodule cathode and sulfide anode, and increases electron liberation from the sulfide ore. This motivates a significant increase in the average extraction rates of Ni, Co, Cu, and Mn in the bacterial solution. The bio-leaching efficiencies of Ni, Co, Cu, and Mn were as high as 95.4%, 97.8%, 92.2% and 97.3%, respectively, representing improvements of 17.1%, 11.5%, 14.3% and 12.9% relative to that of the germ- and Fe(III)-free acidic 9 K basic system. Full article

In this study, a biosensor, based on a glucose oxidase (GO_x) immobilized, carbon-coated tin sulfide (SnS) assembled on a glass carbon electrode (GCE) was developed, and its direct electrochemistry was investigated. The carbon coated SnS (C-SnS) nanoparticle was prepared through a simple two-step process, using hydrothermal and chemical vapor deposition methods. The large reactive surface area and unique electrical potential of C-SnS could offer a favorable microenvironment for facilitating electron transfer between enzymes and the electrode surface. The structure and sensor ability of the proposed GO_x/C-SnS electrode were characterized using scanning electron microscopy (SEM), X-ray diffraction (XRD), Raman spectroscopy, UV–vis spectroscopy, Fourier transform infrared spectroscopy (FTIR), and cyclic voltammetry study (CV). Full article

An electrode system to study the mechanism of fine microgram powder sulfide mineral dissolution was developed by using a relatively simple method that enables the attachment of micrograms of fine powder to a platinum plate surface. This system yields highly reproducible results and is sensitive compared with conventional electrode systems for various sulfide minerals such as pyrite, chalcopyrite, chalcocite, enargite, and tennantite. The leaching behavior of chalcopyrite was re-examined in a test of the application of this electrode system. Chalcopyrite dissolution is enhanced in specific potential regions because it is believed to be reduced to leachable chalcocite, but this result is inconclusive because it is difficult to detect the intermediate chalcocite. Powder chalcopyrite in the new powder electrode system was held at 0.45 V in the presence of copper ion and sulfuric acid media followed by an application of potential in the anodic direction. Besides the chalcopyrite oxidation peak, a small peak resulted at ∼0.55 V; this peak corresponds to reduced chalcocite, because it occurs at the same potential as the chalcocite oxidation peak. Full article