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Lithium–sulfur batteries (LSB) show excellent potential as future energy storage devices with high energy density, but their slow redox kinetics and the shuttle effect seriously hinder their commercial application. Herein, a 0D@2D composite was obtained by anchoring polar nano-TiO2 onto a 2D layered g-C3N4 surface in situ, and a functional separator was prepared using multi-walled carbon nanotubes as a conductive substrate. Due to their long-range conductivity, multi-walled carbon nanotubes make up for the low conductivity of TiO2@g-C3N4 to some extent. A lithium–sulfur battery prepared with a modified separator exhibited excellent long-term cycle performance, a good lithium ion diffusion rate, and rapid redox kinetics. The initial specific discharge capacity of the composite was 1316 mAh g−1 at 1 C, and a high specific discharge capacity of 569.9 mAh g−1 was maintained after 800 cycles (the capacity decay rate per cycle was only 0.07%). Even at the high current density of 5 C, a specific capacity of 784 mAh g−1 was achieved. After 60 cycles at 0.5 C, the modified separator retained the discharge capacity of 718 mAh g−1 under a sulfur load of 2.58 mg cm−2. In summary, the construction of a heterojunction significantly improved the overall cycle stability of the battery and the utilization rate of active substances. Therefore, this study provides a simple and effective strategy for further improving the overall performance and commercial application of lithium–sulfur batteries. [ABSTRACT FROM AUTHOR]

The next generation of all-solid-state batteries can feature battery safety that is unparalleled among conventional liquid batteries. The garnet-type solid-state electrolyte Li7La3Zr2O12 (LLZO), in particular, is widely studied because of its high Li-ion conductivity and stability in air. However, the poor interface-contact between Li and the electrolyte (garnet) severely limits the development of solid electrolytes. In this study, we synthesize cubic phase Li6.4La3Zr1.4Ta0.6O12 (LLZTO) using a secondary sintering method. In addition, a thin aluminum nitride (AlN) layer is introduced between the metal (Li) and the solid electrolyte. Theoretical calculations show that AlN has a high affinity for Li. Furthermore, it is shown that the AlN coating can effectively reduce the interface impedance between Li and the solid electrolyte and improve the lithium-ion transport. The assembled symmetric Li cells can operate stably for more than 3600 h, unlike the symmetric cells without AlN coating, which short-circuited after only a few cycles. The hybrid solid-state battery with a modified layer, which is assembled using LiFePO4 (LFP), still has a capacity of 120 mAh g−1 after 200 cycles, with a capacity retention rate of 98%. This shows that the introduction of an AlN interlayer is very helpful to obtain a stable Li/solid-electrolyte interface, which improves the cycling stability of the battery. [ABSTRACT FROM AUTHOR]

Lithium-sulfur batteries exhibit great potential as one of the most promising energy storage devices due to their high theoretical energy density and specific capacity. However, the shuttle effect of the soluble polysulfide intermediates could lead to a severe self-discharge effect that hinders the development of lithium-sulfur batteries. In this paper, a battery separator has been prepared based on NiFe2O4/Ketjen Black (KB) modification by a simple method to solve the shuttle effect and improve the battery performance. The as-modified separator with the combination of small-size KB and NiFe2O4 nanoparticles can effectively use the physical and chemical double-layer adsorption to prevent polysulfide from the shuttle. Moreover, it can give full play to its catalytic effect to improve the conversion efficiency of polysulfide and activate the dead sulfur. The results show that the NiFe2O4/KB-modified separator battery still maintains a discharge capacity of 406.27 mAh/g after 1000 stable cycles at a high current density of 1 C. Furthermore, the coulombic efficiency remains at 99%, and the average capacity attenuation per cycle is only 0.051%. This simple and effective method can significantly improve the application capacity of lithium-sulfur batteries. [ABSTRACT FROM AUTHOR]

A novel, economic and environmentally friendly anticorrosion coating material for metals is introduced and investigated in this paper. For this purpose, camphor-sulfonic-acid/graphene-doped poly(o-toluidine) composites (MG/CSA@POT) were fabricated using in-situ polymerization with (NH4)2S2O8 as an oxidant. The structure and the morphology of MG/CSA@POT were analyzed using FTIR (Fourier-transform infrared spectroscopy), XRD (X-ray diffraction), and SEM (Scanning Electron Microscope). Multilayer graphene (MG)/CSA@POT-polyurethane composite coatings (MG/CSA@POT-WPU) were prepared on the surface of a carbon steel substrate by mixing MG/CSA@POT with waterborne polyurethane via blending. The corrosion performance of the MG/CSA@POT-WPU composite coatings in a 3.5% NaCl solution was studied with a corrosion electrochemical method. The results showed that 5-MG/CSA@POT-WPU had the best shielding effect on corrosive media and the lowest corrosion rate (1.02 × 10−6 mm/year) compared to other coatings while its inhibition efficiency reached 99.96%. [ABSTRACT FROM AUTHOR]

Electrolytic water splitting with evolution of both hydrogen (HER) and oxygen (OER) is an attractive way to produce clean energy hydrogen. It is critical to explore effective, but low-cost electrocatalysts for the evolution of oxygen (OER) owing to its sluggish kinetics for practical applications. Fe-based catalysts have advantages over Ni- and Co-based materials because of low costs, abundance of raw materials, and environmental issues. However, their inefficiency as OER catalysts has caused them to receive little attention. Herein, the FeS2/C catalyst with porous nanostructure was synthesized with rational design via the in situ electrochemical activation method, which serves as a good catalytic reaction in the OER process. The FeS2/C catalyst delivers overpotential values of only 291 mV and 338 mV current densities of 10 mA/cm2 and 50 mA/cm2, respectively, after electrochemical activation, and exhibits staying power for 15 h. [ABSTRACT FROM AUTHOR]

While the solidification macrostructure of continuous cast billets is an important factor influencing the final performance and rolling yield of oil casing steel, the continuous casting process parameters have a direct influence on the solidification structure. This study simulated the solidification process of the continuous casting round billets of oil casing steel using a cellular automaton–finite element (CAFE) model. According to the simulation results, at a superheat degree of 20–35 K, a casting speed of 1.9–2.1 m/min, and a secondary cooling specific water flow of 0.34–0.45 L/Kg, the solidification structure had a relatively high equiaxed crystal ratio and small average grain radius. Guided by the simulation results, this paper establishes optimal process schemes for producing 26CrMoVTiB steel round billets, comparatively analyzes the equiaxed crystal ratio and central shrinkage of round billets produced according to these schemes, and defines the optimal continuous casting process conditions, which are: superheat degree = 25 K, casting speed = 2.1 m/min, and specific water flow = 0.35 L/Kg. When adopting these process parameters, the 26CrMoVTiB steel round billets demonstrate a tiny central shrinkage and an equiaxed crystal ratio of 45.2%. [ABSTRACT FROM AUTHOR]

In this study, radial crystallization purification method under induction was proposed for preparing 6N,7N ultra-high purity gallium crystal seed. The effect of cooling temperature on the morphology of the crystal seed, as well as the cooling water temperature, flow rate, and the addition amount of crystal seed on the crystallization process was explored, and the best purification process parameters were obtained as follows: temperature of the crystal seed preparation, 278 K; temperature and flow rate of the cooling water, 293 K and 40 L·h−1, respectively; and number of added crystal seed, six. The effects of temperature and flow rate of the cooling water on the crystallization rate were investigated. The crystallization rate decreased linearly with increasing cooling water temperature, but increased exponentially with increasing cooling water flow. The governing equation of the crystallization rate was experimentally determined, and three purification schemes were proposed. When 4N crude gallium was purified by Scheme I, 6N high-purity gallium was obtained, and 7N high-purity gallium was obtained by Schemes II and III. The purity of high-purity gallium prepared by the three Schemes I, II, and III was 99.999987%, 99.9999958%, and 99.9999958%, respectively. [ABSTRACT FROM AUTHOR]

As one of the critical raw materials, very pure gallium is important for the semiconductor and photoelectric industry. Unfortunately, refining gallium to obtain a purity that exceeds 99.99999% is very difficult. In this paper, a new, facile and efficient continuous partial recrystallization method to prepare gallium of high purity is investigated. Impurity concentrations, segregation coefficients, and the purification effect were measured. The results indicated that the contaminating elements accumulated in the liquid phase along the crystal direction. The order of the removal ratio was Cu > Mg > Pb > Cr > Zn > Fe. This corresponded to the order of the experimentally obtained segregation coefficients for each impurity: Cu < Mg < Pb < Cr < Zn < Fe. The segregation coefficient of the impurities depended strongly on the crystallization rate. All observed impurity concentrations were substantially reduced, and the purity of the gallium obtained after our refinement exceeded 99.99999%. [ABSTRACT FROM AUTHOR]