High-entropy Alloys Research Articles

Enhancement in interfacial bonding quality of CoCrFeMnNi high-entropy alloy vacuum hot-compression bonding via surface shot peening

Vacuum hot-compression bonding (VHCB) is an advanced solid-state bonding technique. To expand its application in high-entropy alloys (HEAs), a new strategy to enhance the interfacial bonding quality of CoCrFeMnNi HEA VHCB joints by surface shot peening (SP) was proposed, and the effects of SP treatment on the interfacial bonding behavior and mechanical properties of VHCB joints were investigated. The results revealed that SP treatment introduced a nanocrystalline layer and plastic deformation layer with non-uniform strain on the specimen bonding surface, and a hierarchical grain size gradient fine microstructure was formed by a static recrystallization process under the thermal activation condition before VHCB. During the bonding process, the fine microstructure of the SP-treated layer was retained and provided a large number of grain boundaries and dislocations, which facilitated atomic diffusion and plastic flow in the interfacial region and promoted the closure of interfacial voids and the dissolution of interfacial oxide particles. Additionally, interfacial crystallographic and tensile test analyses indicated that the SP treatment induced a multiple interfacial grain boundary (IGB) migration mechanism in the VHCB joints, which dramatically improved the IGB migration level and ultimately led to a complete recovery of the mechanical properties of the CoCrFeMnNi HEA VHCB joints.

公式章 3 节 1Tribological and electrochemical behaviors of FeCoNiCrMox HEA coatings prepared by internal laser cladding on 316 L steel tube

In order to improve the performance of the inner wall of the 316 L hydraulic cylinder, FeCoNiCrMox (x = 0.2, 0.4, 0.6) high entropy alloy coatings were prepared by laser cladding. The effects of the Mo element on the phase, microstructure, hardness, and tribological as well as electrochemical behaviors of the coating were investigated. The results show that the coatings consist of the FCC phase. The FCC phase increases, and the grain orientation becomes more complex with increased Mo element content. The coatings are mainly composed of columnar and equiaxial crystals. Mo0.4 coating has the finest grain structure, resulting in the coating with a maximum hardness of 421.99 HV, 2.11 times that of the substrate. The nanoindentation test shows that the elastic modulus of the HEA coating increases with the increase of Mo content. The dry sliding wear test shows that adding the Mo element improves the wear performance of the coating. The wear volume loss and wear rate of Mo0.4 coating were the lowest, 12.242 mg and 2.88 × 10−4 mm3•N−1•m−1, respectively. In the 3.5 wt% NaCl solution, the polarization curves and EIS results indicated that adding the Mo element improved the corrosion resistance of the coating. The FeCoNiCrMox coatings significantly improved the hardness, tribological, and electrochemical behaviors of the 316 L substrate.

Crystal-Phase-Engineered High-Entropy Alloy Aerogels for Enhanced Ethylamine Electrosynthesis from Acetonitrile.

Crystal-phase engineering that promoting the rearrangement of active atoms to form new structural frameworks has achieved excellent result in the field of electrocatalysis and optimized the performance of various electrochemical reactions. Herein, for the first time, we found that the different components in metallic aerogels will affect the crystal-phase transformation, especially in high-entropy alloy aerogels (HEAAs), whose crystal-phase transformation during annealing is more difficult than medium-entropy alloy aerogels (MEAAs), but they still show better electrochemical performance. Specifically, PdPtCuCoNi HEAAs with the parent phase of face-centered cubic (FCC) PdCu possess excellent 89.24% of selectivity, 746.82mmol h-1 g-1 cat. of yield rate, and 90.75% of Faraday efficiency for ethylamine during acetonitrile reduction reaction (ARR), while maintaining stability under 50h of long-term testing and 10 consecutive electrolysis cycles. The structure-activity relationship indicates that crystal-phase regulation from amorphous state to FCC phase promotes the atomic rearrangement in HEAAs, thereby optimizing the electronic structure, and enhancing the adsorption strength of reaction intermediates, improving the catalytic performance. This study provides a new paradigm for developing novel ARR electrocatalysts, and also expands the potential of crystal-phase engineering in other application areas. This article is protected by copyright. All rights reserved.

Unique Hierarchically Structured High-Entropy Alloys with Multiple Adsorption Sites for Rechargeable Li-CO2 Batteries with High Capacity.

Lithium-carbon dioxide (Li-CO2) batteries offer the possibility of synchronous implementation of carbon neutrality and the development of advanced energy storage devices. The exploration of low-cost and efficient cathode catalysts is key to the improvement of Li-CO2 batteries. Herein, high-entropy alloys (HEAs)@C hierarchical nanosheet is synthesized from the simulation of the recycling solution of waste batteries to construct a cathode for the first time. Owing to the excellent electrical conductivity of the carbon material, the unique high-entropy effect of the HEAs, and the large number of catalytically active sites exposed by the hierarchical structure, the FeCoNiMnCuAl@C-based battery exhibits a superior discharge capability of 27664 mAh g-1 and outstanding durability of 134 cycles as well as low overpotential with 1.05V at a discharge/recharge rate of 100mA g-1. The adsorption capacity of different sites on the HEAs is deeply understood through density functional theory calculations combined with experiments. This work opens up the application of HEAs in Li-CO2 batteries catalytic cathodes and provides unique insights into the study of adsorption active sites in HEAs.

FeMnNiAlCr High-Entropy Alloys with High-Efficiency Surface Oxide Solar Absorbers for Concentrating Solar Power Systems

FeMnNiAlCr High-Entropy Alloys with High-Efficiency Surface Oxide Solar Absorbers for Concentrating Solar Power Systems

Dependence of Mechanical Properties and Deformation Behavior of TRIP-FeMnCoCrAl Dual-phase High-entropy Alloy on Grain Size and Strain Rate

Dependence of Mechanical Properties and Deformation Behavior of TRIP-FeMnCoCrAl Dual-phase High-entropy Alloy on Grain Size and Strain Rate

Comparison of the Sliding Wear of Single-Phase F.C.C Carbon-Doped Fe40.4Ni11.3Mn34.8Al7.5Cr6 and CoCrFeMnNi High-Entropy Alloys at Cryogenic Temperature

Comparison of the Sliding Wear of Single-Phase F.C.C Carbon-Doped Fe40.4Ni11.3Mn34.8Al7.5Cr6 and CoCrFeMnNi High-Entropy Alloys at Cryogenic Temperature

Microstructure and wear behaviour of AlCoCrFeNi-coated SS316L by atmospheric plasma spray process

ABSTRACT The capacity to endure harsh wear in demanding conditions in stainless steel drops under extreme nature and applications. Protecting the surface by providing a coating layer supports the usage in harsh conditions. In this work, SS316L is coated with AlCoCrFeNi high entropy alloy (HEA) by atmospheric plasma spray process and annealed at 600°C for 2 hours. The AlCoCrFeNi HEA exhibited spherical particles with bcc phase and 20 µm particle size. The coating morphology revealed uniform coating with a homogeneous distribution of HEA particles over a thickness of 150 µm. The coating post annealing offered improved microhardness by 12% than the coated sample before annealing. The wear test was executed by varying load, sliding distance and sliding velocity at normal temperature, 400°C and 600°C and the corresponding worn surface was analysed. The coated samples after annealing showed 57.6%, 87.5% and 65.4% improved wear resistance at normal temperature than the coated sample before annealing at minimum levels of load, sliding velocity and distance. The wear rate of coated and annealed samples revealed 5.2%, 4.5% and 4.4% better wear resistance at 400°C than the coated samples before annealing. The worn surface morphology showcased wear mechanisms to be delamination, abrasive wear, and oxide layer formation under all conditions.

Elemental Influence on Oxidation Behaviour of Cantor‐Based and Refractory High Entropy Alloys: a Critical Review

This article reviews the oxidation behaviour of the two most significant high entropy alloy systems (HEAs) namely Cantor‐based and refractory HEAs. HEAs have been extensively researched and show potential applications in various industries, including marine engine manufacturing, chemical industry, furnaces, ducting, heat exchangers, jet engines, steam turbines, nuclear reactors and electronic devices, among others. Effect of the presence of elements such as aluminium, manganese, chromium, silicon, tantalum, vanadium etc. are studied for catalysing the oxidation of HEAs. Aluminium, chromium and silicon are reportedly found to considerably impact the oxidation kinetics and enhance the oxidation resistance. However, silicon can positively or adversely affect the oxidation resistance depending on its concentration and alloy composition. Other elements like manganese tend to adversely impact the oxidation resistance of FeCoNi‐based HEAs. Refractory elements are typically found to be not suitable for oxidation studies due to the formation of non‐protective oxide layers. However, refractory HEAs offer interesting trends both in terms of enhancing or reducing oxidation resistance depending on the alloying elements. Similarly, findings related to other elements are also presented and elaborated.This article is protected by copyright. All rights reserved.

Kink bands promote exceptional fracture resistance in a NbTaTiHf refractory medium-entropy alloy.

Single-phase body-centered cubic (bcc) refractory medium- or high-entropy alloys can retain compressive strength at elevated temperatures but suffer from extremely low tensile ductility and fracture toughness. We examined the strength and fracture toughness of a bcc refractory alloy, NbTaTiHf, from 77 to 1473 kelvin. This alloy's behavior differed from that of comparable systems by having fracture toughness over 253 MPa·m1/2, which we attribute to a dynamic competition between screw and edge dislocations in controlling the plasticity at a crack tip. Whereas the glide and intersection of screw and mixed dislocations promotes strain hardening controlling uniform deformation, the coordinated slip of <111> edge dislocations with {110} and {112} glide planes prolongs nonuniform strain through formation of kink bands. These bands suppress strain hardening by reorienting microscale bands of the crystal along directions of higher resolved shear stress and continually nucleate to accommodate localized strain and distribute damage away from a crack tip.

Deciphering Indirect Nitrite Reduction to Ammonia in High-Entropy Electrocatalysts Using In Situ Raman and X-ray Absorption Spectroscopies.

This research adopts a new method combining calcination and pulsed laser irradiation in liquids to induce a controlled phase transformation of Fe, Co, Ni, Cu, and Mn transition-metal-based high-entropy Prussian blue analogs into single-phase spinel high-entropy oxide and face-centered cubic high-entropy alloy (HEA). The synthesized HEA, characterized by its highly conductive nature and reactive surface, demonstrates exceptional performance in capturing low-level nitrite (NO2 -) in an electrolyte, which leads to its efficient conversion into ammonium (NH4 +) with a Faradaic efficiency of 79.77% and N selectivity of 61.49% at -0.8 V versus Ag/AgCl. In addition, the HEA exhibits remarkable durability in the continuous nitrite reduction reaction (NO2 -RR), converting 79.35% of the initial NO2 - into NH4 + with an impressive yield of 1101.48 µm h-1 cm-2. By employing advanced X-ray absorption and in situ electrochemical Raman techniques, this study provides insights into the indirect NO2 -RR, highlighting the versatility and efficacy of HEA in sustainable electrochemical applications.

GPa-level pressure-induced enhanced corrosion resistance in TiZrTaNbSn biomedical high-entropy alloy

GPa-level pressure-induced enhanced corrosion resistance in TiZrTaNbSn biomedical high-entropy alloy

Powder Synthesis and Characterization of Al0.5CoCrFeNi High-Entropy Alloy for Additive Manufacturing Prepared by the Plasma Rotating Electrode Process

Powder Synthesis and Characterization of Al_0.5CoCrFeNi High-Entropy Alloy for Additive Manufacturing Prepared by the Plasma Rotating Electrode Process

High-Entropy Alloy Al0.2Co1.5CrFeNi1.5Ti0.5 Prepared from High-Entropy Oxide (Al0.2Co1.5CrFeNi1.5Ti0.5)3O4 by a Deoxidation Process via a CaH2-Assisted Molten Salt Method

High-entropy alloys (HEAs) have attracted a great deal of research interest these days because of their attractive properties. Low-temperature chemical synthesis methods are being developed to obtain nanoscale HEAs with low energy consumption. In this study, we prepared HEA Al0.2Co1.5CrFeNi1.5Ti0.5 nanoparticles from high-entropy oxide (HEO) (Al0.2Co1.5CrFeNi1.5Ti0.5)3O4 by a deoxidation process via a CaH2-assisted molten salt method at 600 °C. X-ray diffraction measurements demonstrated that the oxide precursor and the reduced product have single-phases of spinel structure and face-centered cubic structures, indicating the formation of HEO and HEA, respectively. The HEA nanoparticles exhibited superior catalytic performance in the liquid-phase hydrogenation of p-nitrophenol at room temperature with little leaching of the component elements. Scanning electron microscopy (SEM) with energy-dispersive X-ray spectrometry (EDX) exhibited a good distribution of constituent elements over the HEA nanoparticles in a micro-sized range. However, transmission electron microscopy (TEM) with EDX revealed a slight deviation of elemental distributions of Al and Ti from those of Co, Cr, Fe, and Ni in a nano-sized range, probably due to the incomplete reduction of aluminum and titanium oxides. The elemental homogeneity in the HEA nanoparticles could be improved by taking advantage of the HEO precursor with homogeneous elemental distributions, but the experimental results suggested the importance of the total reduction of oxide precursors to prepare homogeneous HEAs from HEOs.

Phase Evolution and Magnetic Characteristics of CoNiFeCrX (Cu, Al, Mo, Ti, and Pb) High Entropy Alloys

Phase Evolution and Magnetic Characteristics of CoNiFeCrX (Cu, Al, Mo, Ti, and Pb) High Entropy Alloys

Design of refractory high entropy alloys for extreme environment by using CALPHAD

Design of refractory high entropy alloys for extreme environment by using CALPHAD

Noble-Metal-Free High-Entropy Alloy Nanoparticles for Efficient Solar-Driven Photocatalytic CO2 Reduction.

Metal nanoparticle cocatalysts are widely investigated for their ability to enhance the performance of photocatalytic materials, however their practical application is often limited by the inherent instability under light irradiation. This challenge has catalyzed interest in exploring high-entropy alloys (HEAs), which, with their increased entropy and lower Gibbs free energy, provide superior stability. In this study, we successfully synthesized 3.5nm sized noble-metal-free nanoparticles (NPs) composed of a FeCoNiCuMn HEA. With theoretic calculation and experiments, the electronic structure of HEA in augmenting the catalytic CO2 reduction has been uncovered, including the individual roles of each element and the collective synergistic effects. We then investigated their photocatalytic CO2 reduction capabilities when immobilized on TiO2. HEA NPs significantly enhanced the CO2 photoreduction, achieving a 23-fold increase over pristine TiO2, with CO and CH4 production rates of 235.2µ mol g-1 h-1 and 19.9µ mol g-1 h-1, respectively. Meanwhile, HEA NPs showed excellent stability under simulated solar irradiation, as well high-energy X-ray irradiation. This research emphasizes the promising role of HEA nanoparticles, composed of earth-abundant elements, in revolutionizing the field of photocatalysis. This article is protected by copyright. All rights reserved.

Review on the Tensile Properties and Strengthening Mechanisms of Additive Manufactured CoCrFeNi-Based High-Entropy Alloys

The advent of high-entropy alloys (HEAs) provides new possibilities for the metallurgical community. CoCrFeNi-based alloys have been widely recognized to demonstrate superior mechanical properties, amongst the high-entropy alloy systems; in particular, they possess an outstanding tensile ductility and work-hardening capacity. Additive manufacturing (AM) uses a layer-by-layer material deposition approach to build parts directly from computer-aided design models, which are capable of producing near-net-shape HEAs with superior mechanical properties, surpassing traditional manufacturing methods that require a time-consuming post-treatment process, such as cutting, milling, and molding. Moreover, the rapid solidification inherent in AM processes induces the formation of high-density dislocations, which are capable of enhancing the mechanical properties of HEAs. This review comprehensively investigates and summarizes the diverse strengthening mechanisms within CoCrFeNi-based alloys produced using AM technologies, with a specific focus on their influence on tensile properties. A correlation is established between the AM processing parameters and the resultant phases and microstructures, as well as the mechanical properties of CoCrFeNi-based HEAs, which provide guidelines to achieve a superior strength–ductility synergy.

Microstructural evolution and mechanical behavior of novel TiZrTaxNbMo refractory high-entropy alloys

The refractory high-entropy alloy (RHEA) with a body-centered-cubic (BCC) solid-solution structure has excellent high-temperature softening resistance, which has attracted wide interest in the field of high-temperature alloys. However, its limited room-temperature plasticity has greatly hindered its engineering application. To obtain an excellent strength-plasticity matching relationship, in this reported study, the Ta content in the high-entropy alloy (HEA) was adjusted to rectify this shortcoming. A series of TiZrTaxNbMo (x = 1.0, 0.9, 0.8, 0.7, and 0.6 at. percent, at%) RHEAs were prepared using the vacuum arc-melting technique, and the microstructure and mechanical properties of these RHEA alloys were systematically investigated. The experimental results show that the TiZrTaxNbMo RHEAs are composed of main BCC1 and minor BCC2 phases, which exhibit a dendritic structure. By reducing the Ta content, the elemental segregation caused by the non-equilibrium solidification is reduced. In terms of mechanical properties, with the decrease of Ta content, the hardness and room-temperature yield strength of the alloy decreases slightly, but the room-temperature plasticity increases significantly. The Ta0.7 alloy has the highest plasticity (34.8 %), which is about twice that of the equimolar Ta 1.0 alloy, while the yield strength remained at 1297 MPa. The excellent mechanical properties of the alloys can be attributed to solid-solution strengthening and the formation of moderate amounts of interdendritic regions. The interaction between slip bands and dislocations formed during compression of the Ta0.7 alloy decreased its work hardening. Moreover, the theoretical model of solid-solution strengthening elucidates that the calculated values of the alloy’s yield strength are consistent with that obtained experimentally.

Competitive segregation to grain boundaries between Cr and Co in FeNiCrCo alloy

Alloying elements segregating to grain boundaries (GBs) is vital in determining structural stability and mechanical properties of alloys, especially in high‐entropy alloys (HEAs) that consist of multiple elements. However, some details remain unclear, such as the process of varied atoms (Cr and Co) cosegregation to GBs in FeNiCrCo alloy. Therefore, the competition and cooperation between Fe, Ni, Cr, and Co atoms segregating to GBs of FeNiCrCo alloy were investigated via molecular dynamic (MD) simulation. Five [110] symmetric tilt GBs of FeNiCrCo were applied to study the relation between the tendency of atomic segregation especially Cr and Co and GB characters including GB energy and GB excess free volume (GB excess volume). A competitive segregation phenomenon between Cr and Co atoms was discovered, which could be dominated by GB excess volume and different atomic radii among components.