Oxygen-Bridged Cobalt-Chromium Atomic Pair in MOF-Derived Cobalt Phosphide Networks as Efficient Active Sites Enabling Synergistic Electrocatalytic Water Splitting in Alkaline Media.

Electrochemical water splitting offers a most promising pathway for "green hydrogen" generation. Even so, it remains a struggle to improve the electrocatalytic performance of non-noble metal catalysts, especially bifunctional electrocatalysts. Herein, aiming to accelerate the hydrogen and oxygen evolution reactions, an oxygen-bridged cobalt-chromium (Co-O-Cr) dual-sites catalyst anchored on cobalt phosphide synthesized through MOF-mediation are proposed. By utilizing the filling characteristics of 3d orbitals and modulated local electronic structure of the catalytic active site, the well-designed catalyst requires only an external voltage of 1.53 V to deliver the current density of 20 mA cm-2 during the process of water splitting apart from the superb HER and OER activity with a low overpotential of 87 and 203 mV at a current density of 10 mA cm-2 , respectively. Moreover, density functional theory (DFT) calculations are utilized to unravel mechanistic investigations, including the accelerated adsorption and dissociation process of H2 O on the Co-O-Cr moiety surface, the down-shifted d-band center, a lowered energy barrier for the OER and so on. This work offers a design direction for optimizing catalytic activity toward energy conversion.

Design Strategies for Perovskite-Type High-Entropy Oxides with Applications in Optics.

It is essential and challenging to develop advanced ceramic materials with thermal stability and high reflectivity for optical fields. Encouragingly, recent breakthroughs and significant advances in high-entropy ceramics have made high-entropy oxides a potential candidate material for optical applications. Therefore, in this study, we analyzed the effect of lattice distortion on the design of high-reflectivity, high-entropy oxides using first-principles calculations and aberration-corrected microscopy. In order to optimize the optical properties of the materials, a series of novel perovskite-type high-entropy oxides, (LaxK0.4-xCa0.2Sr0.2Ba0.2)TiO3+δ (x = 0.1, 0.15, 0.2, 0.25, 0.3), were designed and synthesized using solid-state sintering based on the charge conservation principle and bond energy principle. When the content of La in the A-site element was 30%, the optical reflectivity reached 94% by suppressing the oxygen vacancy. Furthermore, we have successfully prepared a series of coatings by air spraying based on the regulation of the mass ratio of resin and powder. Compared to the uncoated substrate, the backside temperature can be reduced by 41%. This work provides a feasible design route with the first clear guidelines for highly reflective high-entropy ceramic materials and enables highly stable material design in multielement spaces.

Arsenic release pathway and the interaction principle among major species in vacuum sulfide reduction roasting of copper smelting flue dust.

The efficient release of arsenic in copper smelting flue dust (CSFD) with complicated production conditions and composition under the premise of environmental safety is difficult for the copper smelting industry. The vacuum environment is conducive to the volatilization of low-boiling arsenic compounds, which is beneficial to the physical process and chemical reaction of increasing the volume. In the present study, combined with thermodynamic calculations, the roasting process of pyrite and CSFD mixed in proportion in vacuum was simulated. Additionally, the release process of arsenic and the interaction mechanism of the main phases were performed in detail. The addition of pyrite facilitated the decomposition of stable arsenate in CSFD into volatile arsenic oxides. The results indicated that exceeding 98% of arsenic in CSFD volatilized into the condenser, while the arsenic content in the residue was reduced to 0.32% under optimal conditions. Pyrite could reduce the oxygen potential during the chemical reaction with CSFD, reacting with sulfates in CSFD to convert into sulfides and magnetic iron oxide (Fe3O4) simultaneously, and Bi2O3 would be transformed into metallic Bi. These findings are significant for developing arsenic-containing hazardous waste treatment routes and the application of innovative technical approaches.

Thermal Stability, Optical and Electrical Properties of Substoichiometric Molybdenum Oxide.

Substoichiometric molybdenum oxide ceramics have aroused widespread interest owing to their promising optical and electrical performance. In this work, the thermal stability and decomposition mechanism of Mo9O26 and Mo4O11 at 700-1000 °C and 700-1100 °C were investigated, respectively. Based on this information, MoOx (2 < x < 3) bulk ceramics were prepared by spark plasma sintering (SPS). The results show that Mo9O26 is stable up to 790 °C in an argon atmosphere. As the temperature rises, it decomposes into Mo4O11. Mo4O11 can exist stably at 830 °C, beyond which it will convert to MoO2. The MoOx ceramic bulks with four different components (MoO2.9, MoO2.8, MoO2.7 and MoO2.6) were successfully sintered by SPS, and their relative density was greater than 96.4% as measured by the Archimedes principle. The reflectivity of MoOx ceramic bulk is low and only 6.3% when the composition is MoO2.8. The resistivity increases from 10-3 to 10-1 Ωcm with the increase in the O/Mo atomic ratio x. In general, the thermal stability information provides a theoretical basis for the processing of MoOx materials, such as the sintering of the MoOx target. The optical and electrical properties show that MoOx is a low-reflective conductive oxide material with great photoelectric application value.

Electrolysis Synthesis of Carbides and Carbon Dioxide Capture in Molten Salts.

The application of carbides in catalysis, batteries, aerospace fields, etc. has been continuously expanded and deepened, which is attributed to the diversified physicochemical properties of carbides via a tune-up of their morphology, composition, and microstructure. The emergence of MAX phases and high entropy carbides with unparalleled application potential undoubtedly further stimulates the research upsurge of carbides. The traditional pyrometallurgical or hydrometallurgical synthesis of carbides inevitably faces the shortcomings of complex process, unacceptable energy consumption, extreme environmental pollution, and beyond. The molten salt electrolysis synthesis method with the superiorities of straightforward route, high efficiency, and environmental friendliness has demonstrated its validity in the synthesis of various carbides, which naturally initiates more research. In particular, the process can achieve CO2 capture while synthesizing carbides based on the excellent CO2 capture capability of some molten salts, which is of great significance for carbon neutralization. In this paper, the synthesis mechanism of carbide by molten salt electrolysis, the process of CO2 capture and carbides conversion, the latest research progress in the synthesis of binary, ternary, multi-component, and composite carbides are reviewed. Finally, the challenges, development perspectives, and research directions of electrolysis synthesis of carbides in molten salts are featured.

Research on Spheroidization of Tungsten Powder from Three Different Raw Materials.

In this work, three kinds of tungsten powders with different particle sizes were spheroidized by radio-frequency (RF) inductively coupled plasma spheroidization. The spheroidization behavior of these tungsten powders was investigated and compared. The spheroidization effects of irregular tungsten powder improves with the decrease in degree of agglomeration and increases with primary particle size. Spherical tungsten powder from irregular powder with a primary particle size of 19.9 µm and an agglomeration coefficient of 1.59 had the best spheroidization effect; its apparent density, hall flow time, and spheroidization ratio are 9.36 g/cm3, 6.28 s/50 g, and 98%, respectively. The results show that irregular feedstock tungsten powder with a smaller primary particle size and higher agglomeration degree has a poor spheroidization effect because it is easily affected by the gas flow and deviates from the high temperature zone. On the contrary, irregular feedstock tungsten powder with larger primary particle sizes and lower agglomeration degrees has better spheroidization effects.

Enhanced Strength and Hardness of AS41 Magnesium Alloy Fabricated by Selective Laser Melting.

AS41 magnesium alloy possesses outstanding performance features such as light weight, high strength to toughness ratio and excellent heat resistance due to the addition of Si element, while traditional casting methods are prone to inducing large grain size and coarse Mg2Si phase. In this study, we first reported utilizing the selective laser melting (SLM) technique, fabricating AS41 samples and exploring the effect of laser energy densities on the metallurgical quality by characterizing and investigating the microstructure and mechanical properties. Results showed that the optimal laser energy density range was 60 to 100 J/mm3. Average grain size of only 2.9 µm was obtained with weak texture strength of 1.65 in {0001} orientation. Meanwhile, many dispersed secondary ß-Mg17Al12 and Mg2Si phases were distributed inside the α-Mg matrix. It was confirmed that the SLM process introduced more grain recrystallization, inducing giant high-angle grain boundaries (HAGBs) and hindering the movement of dislocations, therefore forming dislocation strengthening while achieving grain refinement strengthening. Finally, three times the ultimate tensile strength of 313.7 MPa and higher microhardness of 96.4 HV than those of the as-cast state were obtained, verifying that the combined effect of grain refinement, solid solution strengthening and precipitation strengthening was responsible for the increased strength. This work provides new insight and a new approach to preparing AS41 magnesium alloy.

Novel Efficient Reduction Route for Magnesium Production Using Silicothermic Process.

A novel efficient reduction route was developed for preparing porous pellets to enhance mass transfer during magnesium production, which can improve the reactivity of pellet reaction to improve the reduction efficiency. A porous pellet precursor was prepared at 150 MPa using NH4HCO3 as a pore-forming agent, and the reaction characteristics of the pellets with 0, 5%, 10%, 20%, and 30% pore-forming agents were measured under a high vacuum of approximately 10 Pa heat-treated from 100 °C to 1400 °C. The results showed that the instantaneous maximum reduction rate first increased and then decreased with the increase in pore-forming agents. When the reduction conversion was 80%, the reduction efficiency of pellets with 5% pore-forming agent was 36% greater than that without pore-forming agent pellets. When the reduction conversion was 90%, the reduction efficiency of pellets with 5% pore-forming agent was 29% greater than that without pore-forming agent pellets. The results indicate that the diffusion rate of magnesium vapor in pellets is significantly increased; the time of chemical reaction reaching equilibrium is shortened; the chemical reaction rate and the magnesium production efficiency are increased by adding a proper ratio of NH4HCO3 compared to that obtained without NH4HCO3 at the identical reduction temperature.

An Enhanced Positional Error Compensation Method for Rock Drilling Robots Based on LightGBM and RBFN.

Rock drilling robots are able to greatly reduce labor intensity and improve efficiency and quality in tunnel construction. However, due to the characteristics of the heavy load, large span, and multi-joints of the robot manipulator, the errors are diverse and non-linear, which pose challenges to the intelligent and high-precision control of the robot manipulator. In order to enhance the control accuracy, a hybrid positional error compensation method based on Radial Basis Function Network (RBFN) and Light Gradient Boosting Decision Tree (LightGBM) is proposed for the rock drilling robot. Firstly, the kinematics model of the robotic manipulator is established by applying MDH. Then a parallel difference algorithm is designed to modify the kinematics parameters to compensate for the geometric error. Afterward, non-geometric errors are analyzed and compensated by applying RBFN and lightGBM including features and kinematics model. Finally, the experiments of the error compensation by combing combining the geometric and non-geometric errors verify the performance of the proposed method.

Study on Hardness, Microstructure, Distribution of the Self-lubricating Phase, Friction and Wear Property of 1Cr13MoS after Heat Treatment.

1Cr13MoS is a kind of material with excellent corrosion resistance and good mechanical properties. Meanwhile, it also has good self-lubricating properties due to the presence of molybdenum disulfide phase inside the material and can be used as friction pair material in the pump. In this paper, the hardness, microstructure, distribution of the self-lubricating phase, friction and wear properties of 1Cr13MoS after heat treatment were studied. After quenching at 1000 °C and tempering at 520 °C, the hardness of 1Cr13MoS prepared by pyrometallurgy is higher than that of HB 350. The tempering sorbite structure is evenly distributed, and the self-lubricating phase MoS2 is discretely distributed on the substrate with the average size is about 6 µm, which leads to good friction and wear properties. It is worth noting that the 1Cr13MoS is actually operated as friction pair material on the water pump and has a significant wear improvement effect compared to the conventional 12% chrome steel series.

Extent of the Oxidative Side Reactions to Peptides and Proteins During the CuAAC Reaction.

The copper-catalyzed azide-alkyne cycloaddition (CuAAC) reaction is a powerful tool for bioconjugation of biomolecules, particularly proteins and peptides. The major drawback limiting the use of the CuAAC reaction in biological systems is the copper-mediated formation of reactive oxygen species (ROS), leading to the oxidative degradation of proteins or peptides. From the studies on a limited number of proteins and peptides, it is known that, in general, the copper mediated oxidative damage is associated with the copper coordination environment and solvent accessibility. However, there is a lack of data to help estimate the extent of copper-mediated oxidation on a wide range of proteins and peptides. To begin to address this need, we quantitatively measured the degree of copper-mediated oxidation on libraries of 1200 tetrapeptides and a model protein (bovine serum albumin, BSA) using liquid chromatography mass spectrometry (LC-MS). The collected data will be useful to researchers planning to use the CuAAC reaction for bioconjugaton on peptides or proteins.

[New approach in the explaining of the Morgan Law in genetics teaching].

Using the model of broad and narrow way, the paper introduces a new approach in the explaining of a few basic concepts in the Morgan Law. The paper introduces a thorough inquiry into the applying condition of the three-factor crosses, and finds the source of the difference between the crossover frequency (F(C)) and recombination frequency (F(R)) of the non-adjacent factors in the three-factor crosses in Neurospora crassa.