Supercapacitors (SCs), one of the most popular types of energy-storage devices, present lots of advantages, such as large power density and fast charge/discharge capability. Being the promising SCs electrode materials, metal–organic frameworks (MOFs) and their derivatives have gained ever-increasing attention due to their large specific surface area, controllable porous structure and rich diversity. Herein, the recent development of MOFs-based materials and their application in SCs as the electrode are reviewed and summarized. The preparation method, the morphology of the materials and the electrical performance of various MOFs and their derivatives (such as carbon, metal oxide/hydroxide and metal sulfide) are briefly discussed. Most of recent works concentrate on Ni-, Co- and Mn-MOFs and their composites/derivatives. Conclusions and our outlook for the researches are also given, which would be a valuable guideline for the rational design of MOFs materials for SCs in the near future.

In this study, a combination of Al–12Si and Al–20Si (Al–(12-20)Si) alloys was fabricated by selective laser melting (SLM) as a result of increased component requirements such as geometrical complexity and high dimensional accuracy. The microstructure and mechanical properties of the SLM Al–(12-20)Si in as-produced as well as in heat-treated conditions were investigated. The Al–(12-20)Si interface was in the as-built condition and it gradually became blurry until it disappeared after heat treatment at 673 K for 6 h. This Al–(12-20)Si bi-material displayed excellent mechanical properties. The hardness of the Al–20Si alloy side was significantly higher than that of the Al–12Si alloy side and the disparity between both sides gradually decreased and tended to be consistent after heat treatment at 673 K for 6 h. The tensile strength and elongation of the Al–(12-20Si) bi-material lies in between the Al–12Si and Al–20Si alloys and fracture occurs in the Al–20Si side. The present results provide new insights into the fabrication of bi-materials using SLM.

To develop promising adsorbent candidates for adsorptive denitrogenation, we screened the adsorption of NO, NO₂, and NH₃ in 19 M-HKUST-1 (M = Be, Fe, Ni, Cr, Co, Cu, V, Zn, Mo, Mn, W, Sn, Ti, Cd, Mg, Sc, Ca, Sr, and Ba) systematically using first-principle calculations. Of these, four variants of M-HKUST-1 (M = Ni, Co, V, and Sc) yield more negative adsorption Gibbs free energy ΔG_ads than the original Cu-HKUST-1 for three adsorbates, suggesting stronger adsorbate binding. Ti-HKUST-1, Sc-HKUST-1, and Be-HKUST-1 are predicted to have the largest NO, NO₂, and NH₃ adsorption energies within the screened M-HKUST-1 series, respectively. With the one exception of NO₂ dissociation on V-HKUST-1, dissociative adsorption of NO, NO₂, and NH₃ molecules on the other considered M-HKUST-1 is energetically less favorable than molecular adsorption thermodynamically. The barrier calculations show that the dissociation is difficult to occur on Cu-HKUST-1 kinetically due to the very large dissociation barrier. Electronic analysis is provided to explain the bond nature between the adsorbates and M-HKUST-1. Note that the isostructural substitution of Cu to the other metals is a major simplification of the system, representing the ideal situation; however, the present study provides interesting targets for experimental synthesis and testing.

The Al-20Si-5Fe-3Cu-1Mg alloy was fabricated using selective laser melting (SLM). The microstructure and properties of the as-prepared SLM, post-treated SLM, and SLM with substrate plate heating are studied. The as-prepared SLM sample shows a non-uniform microstructure with four different phases: fcc-αAl, eutectic Al-Si, Al₂MgSi, and δ-Al₄FeSi₂. With thermal treatment, the phases become coarser and the δ-Al₄FeSi₂ phase transforms partially to β-Al₅FeSi. The sample produced with SLM substrate plate heating shows a relatively uniform microstructure without a distinct difference between hatch overlaps and track cores. Room temperature compression test results show that an as-prepared SLM sample reaches a maximum strength (862 MPa) compared to the heat-treated (524 MPa) and substrate plate heated samples (474 MPa) due to the presence of fine microstructure and the internal stresses. The reduction in strength of the sample produced with substrate plate heating is due to the coarsening of the microstructure, but the plastic deformation shows an improvement (20%). The present observations suggest that substrate plate heating can be effectively employed not only to minimize the internal stresses (by impacting the cooling rate of the process) but can also be used to modulate the mechanical properties in a controlled fashion.