Dry Sliding of Nitrided NiTiHf

The unlubricated friction and wear properties of the superelastic material NiTiHf, treated by either gas nitriding or plasma nitriding, have been investigated. Pin-on-disk testing of the studied materials was performed at sliding speeds from 0.01 to 1 m/s at normal loads of 1, 5, or 10 N. For all of the studied friction pairs (NiTiHf pins vs. nitrided disks) over the given parameters, the steady-state coefficients of friction varied from 0.7 to 1.6, and those of the control (NiTiHf on NiTiHf) varied from 0.5 to 1.2. Pin wear factors ranged from approximately 10^?6 against the NiTiHf and plasma-nitrided disks to approximately 10^?4 for the gas-nitrided disks. The plasma-nitrided disks provided wear protection in several cases and tended to wear by adhesion. The gas-nitrided treatment generated the most pin wear but essentially no disk wear except under the most severe of the studied conditions (1 N load and 1 m/s sliding speed). The results of this study are expected to provide guidance for design of aerospace components such as gears and fasteners.     

Corrosion of structural constituents of 2017 aluminium alloy in acidic solutions containing inhibitors

The objective of this study is to establish the corrosion behaviour of the most important structural constituents of the aluminium alloy 2017 in orthophosphoric acid solutions containing heteropolyoxomolybdate, tungstate and vanadate. These are potential candidates for replacing toxic hexavalent chromium species in stripping solution for anodic coatings. The corrosion rate of the alloy is estimated with linear polarisation method. It decreases from 0.58 mA cm⁻² in uninhibited solution to 0.10 mA cm⁻² in a solution containing heteropolyoxomolybdate species. Microscopic studies reveal that heteropolyoxomolybdate species inhibit corrosion of the matrix and intermetallic Al₁₅(Fe,Mn)₃(Si,Cu)₂ but not Mg₂Si. Intermetallic Al₂Cu remains not corroded. Heteropolyoxotungstate species virtually do not inhibit the corrosion of the alloy. The solution containing vanadium species is not stable with time and the corrosion rate is not determined. Nevertheless, corrosion of the matrix is inhibited, but intermetallics Al₁₅(Fe,Mn)₃(Si,Cu)₂ together with Mg₂Si are dissolved. X-ray photoelectron spectroscopy is used for examination of a corrosion product precipitated on the surface.     

Fabrication of Ni3AI by hot pressing from element powders

Ni3Al intermetaUic was synthesized by hot pressing from element powders of nickel, aluminum, and boron. The influences of parameters on the properties of Ni3Al were investigated. The parameters include the particle size of nickel powder, adding or without boron powder, hot pressing temperature, etc. The properties include the density of hot-pressed samples, resultant redo of Ni3A1 phase, and bending strength. The microstructures of hot-pressed samples were investigated by X-ray diffraction and scan electronic microscopy, and the properties, such as density and bending strength, were also measured. The results show that a higher bending strength was obtained under the same hot pressing conditions by the fine nickel powder than the coarse one, and there is little difference about density. Boron powder added in this process accelerates the formation of Ni3Al and markedly increases the hot pressed density. In the temperature range of this study, the density increases along with the hot pressing temperature. Full dense Ni3Al samples were obtained under the condition of 860℃, 10 min, 45 MPa from Ni-22.89A1-0.5B powder.     

Debye temperature, self-diffusion and elastic constants of intermetallic compounds

The Debye temperature of a material is a suitable parameter to describe phenomena of solid-state physics which are associated with lattice vibrations. It basically depends on the elastic constants. In recent work a simple method was put forward that allows one to derive precise Debye temperatures of crystals with cubic, hexagonal and tetragonal symmetry from the elastic constants. The type of chemical binding does not play any role. It is one aim of the present work to apply this method to various intermetallic compounds, i.e. to critically analyse published Debye temperatures and to calculate hitherto unknown values. It is a further aim to show that the activation energy of self-diffusion is also connected with the elastic constants by a simple law at least for the cubic B2 and L1₂ intermetallics, as it was recently found for face-centred cubic metals. Some consequences for high-temperature plasticity are discussed.     

MOF‐Confined Sub‐2 nm Atomically Ordered Intermetallic PdZn Nanoparticles as High‐Performance Catalysts for Selective Hydrogenation of Acetylene

Controllable synthesis of ultrasmall atomically ordered intermetallic nanoparticles is a challenging task, owing to the high temperature commonly required for the formation of intermetallic phases. Here, a metal–organic framework (MOF)‐confined co‐reduction strategy is developed for the preparation of sub‐2 nm intermetallic PdZn nanoparticles, by employing the well‐defined porous structures of calcinated ZIF‐8 (ZIF‐8C) and an in situ co‐reduction therein. HAADF‐STEM, HRTEM, and EDS characterizations reveal the homogeneous dispersion of these sub‐2 nm intermetallic PdZn nanoparticles within the ZIF‐8C frameworks. XRD, XPS, and EXAFS measurements further confirm the atomically ordered intermetallic phase nature of these sub‐2 nm PdZn nanoparticles. Selective hydrogenation of acetylene evaluation results show the excellent catalytic properties of the sub‐2 nm intermetallic PdZn, which result from the energetically more favorable path for acetylene hydrogenation and ethylene desorption over the ultrasmall particles than over larger‐sized intermetallic PdZn as revealed by density functional theory (DFT) calculations. Moreover, this protocol is also extendable for the preparation of sub‐2 nm intermetallic PtZn nanoparticles and is expected to provide a novel methodology in synthesizing ultrasmall atomically ordered intermetallic nanomaterials by rationally functionalizing MOFs.     

Fe-Al金属间化合物氢脆效应研究现状

Fe-Al金属间化合物具有良好的抗氧化、抗硫化腐蚀性能以及高温结构性质,而且质轻价廉,在航空航天、汽车工业、能量转换系统、过滤材料等领域具有广阔的应用前景,但在室温下易发生环境脆化,这也是其未能得到大规模应用的主要原因。本文在介绍Fe-Al金属间化合物特性的基础上,重点综述了Fe-Al金属间化合物氢脆行为及其机制的实验和理论研究进展,提出了今后的研究方向。     

Local Photothermal Control of Phase Transitions for On-Demand Room-Temperature Rewritable Magnetic Patterning

The ability to make controlled patterns of magnetic structures within a nonmagnetic background is essential for several types of existing and proposed technologies. Such patterns provide the foundation of magnetic memory and logic devices, allow the creation of artificial spin-ice lattices, and enable the study of magnon propagation. Here, a novel approach for magnetic patterning that allows repeated creation and erasure of arbitrary shapes of thin-film ferromagnetic structures is reported. This strategy is enabled by epitaxial Fe_0.52Rh_0.48 thin films designed so that both ferromagnetic and antiferromagnetic phases are bistable at room temperature. Starting with the film in a uniform antiferromagnetic state, the ability to write arbitrary patterns of the ferromagnetic phase is demonstrated by local heating with a focused laser. If desired, the results can then be erased by cooling below room temperature and the material repeatedly re-patterned.     

Stabilization of Sn Anode through Structural Reconstruction of a Cu–Sn Intermetallic Coating Layer

The metallic tin (Sn) anode is a promising candidate for next-generation lithium-ion batteries (LIBs) due to its high theoretical capacity and electrical conductivity. However, Sn suffers from severe mechanical degradation caused by large volume changes during lithiation/delithiation, which leads to a rapid capacity decay for LIBs application. Herein, a Cu–Sn (e.g., Cu₃Sn) intermetallic coating layer (ICL) is rationally designed to stabilize Sn through a structural reconstruction mechanism. The low activity of the Cu–Sn ICL against lithiation/delithiation enables the gradual separation of the metallic Cu phase from the Cu–Sn ICL, which provides a regulatable and appropriate distribution of Cu to buffer volume change of Sn anode. Concurrently, the homogeneous distribution of the separated Sn together with Cu promotes uniform lithiation/delithiation, mitigating the internal stress. In addition, the residual rigid Cu–Sn intermetallic shows terrific mechanical integrity that resists the plastic deformation during the lithiation/delithiation. As a result, the Sn anode enhanced by the Cu–Sn ICL shows a significant improvement in cycling stability with a dramatically reduced capacity decay rate of 0.03% per cycle for 1000 cycles. The structural reconstruction mechanism in this work shines a light on new materials and structural design that can stabilize high-performance and high-volume-change electrodes for rechargeable batteries and beyond.     

Main recent contributions to SHS from France

Both in situ TRXRD and IR thermography, on the one hand, and different levels of modeling, on the other, have generated a strong progress in the knowledge and control of numerous SHS reactions. The SHS of simple binary materials, such as intermetallics (FeAl, MoSi₂, NbAl₃, etc.), oxides (e.g. ZrO₂), carbides (e.g. SiC) or nitrides, more complex materials, such as mullite, SiAlONs, MAX phases, composites (SiO₂-Al₂O₃, NiAl-ZrO₂), powders in their more complicated states, such as well controlled microstructures, fully densified intermetallics, smart composites, and hard coatings carried out by GFA researchers greatly contributed to the worldwide competition to harness the potential of SHS. On the occasion of the 40th anniversary of SHS, this paper is giving an overview of the main results obtained by GFA over the last ten years. Dominique Vrel (LIMHP UPR 1311 CNRS-Paris XIII, Villetaneuse)