Two‐dimensional transition metal dichalcogenides (2D TMDs) present promising applications in various fields such as electronics, optoelectronics, memory devices, batteries, superconductors, and hydrogen evolution reactions due to their regulable energy band structures and unique properties. For emerging spintronics applications, materials with excellent room‐temperature ferromagnetism are required. Although most transition metal compounds do not possess room‐temperature ferromagnetism on their own, they are widely modified by researchers using the emerging strategies to engineer or modulate their intrinsic properties. This paper reviews recent enhancement approaches to induce magnetism in 2D TMDs, mainly using doping, vacancy defects, composite of heterostructures, phase modulation, and adsorption, and also by electron irradiation induction, O plasma treatment, etc. On this basis, the produced effects of these methods for the introduction of magnetism into 2D TMDs are compressively summarized and constructively discussed. For perspective, research on magnetic doping techniques for 2D TMDs materials should be directed toward more reliable and efficient directions, such as exploring advanced design strategies to combine dilute magnetic semiconductors, antiferromagnetic semiconductors, and superconductors to develop new types of heterojunctions; and advancing experimentation strategies to fabricate the designed materials and enable their functionalities with simultaneously pursuing the upscalable growth methods for high‐quality monolayers to multilayers.

Many urgently needed inconel superalloy parts with complex internal cavity geometry and high surface precision are difficult to prepare by traditional subtractive manufacturing methods because of its poor machinability. The additive manufacturing technology that has emerged in recent years became a research hotspot in the manufacture of refractory and difficult-to-process metals. In the present study, selective laser melting (SLM), a typical additive manufacture technology, was used to prepare Inconel 718 samples. The influences of input laser energy density ((E, J/mm³) on densification behavior, phases composition, microstructures, microhardness, and wear performance of the SLM as-built Inconel 718 samples were explored in detail. X-ray diffraction (XRD), optical microscopy (OM), scanning electron microscopy (SEM), and transmission electron microscopy (TEM) were used to examine the phase composition and microstructure evolutions. The results show that the formablity, microstructures and mechanical properties of the printed samples were all improved with the increase of E within the parameter setting range of this study. At a lower E, the poor surface morphology and balling effect occurred, the density, hardness, and wear resistance were all at a relatively lower level. When an E value of 190 J/mm was properly set, the surface open-pores and balling effect disappeared, the laser scanning tracks became smooth and continuous, the near-full dense (99.15%) and specimens with good metallurgical bonding and no critical defect were obtained, in which the average microhardness value reached 348 HV_0.2 and wear rate was 5.67 × 10⁻⁴ mm³/N·m. The homogeneity of the superalloy Inconel 718 was also explored.

Metal organic frameworks (MOFs) are widely used as precursors due to their tunable morphology and high specific surface area. Molybdenum nitride (MoN) and molybdenum carbide (Mo₂C) are promising catalyst materials with electronic structures similar to the noble metal platinum. However, the preparation and modification of the composite systems comprising MoN and Mo₂C are complex, often leading to significant agglomeration and limiting their application in various catalytic fields. In this work, we designed and developed a novel bimetallic Co-MOFs-Mo with a stable and unique framework morphology. By varying the organic ligand content, we controlled the morphology and enhanced the intrinsic electrocatalytic activity through Mo doping. Using the Co-MOFs-Mo sample as the Co source, we fabricated a Co-Mo_xN/Mo₂C catalytic material with a special framework structure. Compared to Mo₂N and Mo₂N/Mo₂C, this catalyst exhibits a larger specific surface area and superior performance in both hydrogen evolution reaction (HER) and oxygen evolution reaction (OER). The Co-Mo_xN/Mo₂C catalyst achieves an HER overpotential of 297 mV at a current density of 10 mA·cm^-2 and an OER overpotential of 480 mV at 20 mA·cm^-2. This research provides valuable insights into the rational design of molybdenum-based noble-metal-free catalyst materials.