L10 Phase Research Articles

Achieving a remarkable strength–ductility combination in a novel casting AlCoCrNi high entropy alloy

We prepared a novel cast high-entropy alloy (HEA) that comprises a dual-phase microstructure with L12 and B2 phases. Our designed HEA achieved a remarkable strength–ductility balance (tensile strength of ∼1025 MPa and uniform elongation of ∼30 %, which well outperforms many as-cast HEAs including arc-melting and directly cast HEAs.

Superior strain-hardening and strength-ductility synergy by hierarchical L12 phases in a highly (Al, Ti)-added medium-entropy alloy

A novel precipitate-strengthened Co–Cr–Ni medium-entropy alloy with a pure “FCC + L12” dual-phase structure is developed by adding a high concentration (6 at.%) of Al and Ti elements. After aging heat treatment at 700 °C for 4 h, the hierarchical L12 phases, composed of primary large-sized L12 phases (∼70 nm) and secondary L12 particles (∼14 nm), are achieved. The designed alloy featuring hierarchical L12 phases exhibits excellent strength-ductility combinations and strain-hardening ability, properties that are much improved over their counterparts with homogeneous dispersed L12 phases (∼13 nm) and without L12 phases. Especially, the yield strength (1320 MPa), ultimate tensile strength (1886 MPa), and average strain-hardening rate (5.15 GPa) are obtained in the alloy with hierarchical L12 precipitates deformed at cryogenic temperature. The Orowan bypass mechanism of the primary L12 phases, along with the shearing mechanism of the secondary L12 phases, collectively contributes to the exceptional strength of the alloy with hierarchical L12 precipitates. The penetration of dislocations and stacking faults (SFs) in the primary L12 phases, combined with hetero-deformation-induced (HDI) hardening attributed to these hierarchical L12 precipitates, may be a key factor in improving strain-hardening properties of the alloy.

Variation of the Passive Film on Compositionally Concentrated Dual-Phase Al0.3Cr0.5Fe2Mn0.25Mo0.15Ni1.5Ti0.3 and Implications for Corrosion

AbstractThe passive film on a dual-phase Al0.3Cr0.5Fe2Mn0.25Mo0.15Ni1.5Ti0.3 FCC + Heusler (L21) compositionally concentrated alloy formed during extended exposure to an applied potential in the passive range in dilute chloride solution was characterized. Each phase, with its own distinct composition of passivating elements, formed unique passive films separated by a heterophase interface. High-resolution, surface sensitive characterization enabled chemical analysis of the passive film formed over individual phases. The film formed over the L21 phase had a higher concentration of Al, Ni, and Ti, while the film formed over FCC phase was of similar thickness but contained comparatively higher Cr, Fe, and Mo concentrations, consistent with the differences in bulk microstructure composition. The passive film was continuous across phase boundaries and the distribution of passivating elements (Al, Cr, and Ti) indicated both phases were independently passivated. Spatially resolved analysis of the surface chemistry of the dual-phase CCA revealed that the cation with the highest composition in passive film formed on the FCC phase was Cr (52.4 at. pct) and for the L21 phase was Ti (53.1 at. pct) despite the bulk concentration of each element being below 20 at. pct in their respective phases. Al, Cr, and Ti were enriched in both phases within the passive film relative to their respective bulk compositions. In parallel studies, single-phase alloys with compositions representative of the FCC and L21 phases were synthesized to evaluate the corrosion behavior of each phase in isolation. The corrosion behavior of the dual-phase alloy showed passivity evidenced by a pitting potential of 0.615 VSCE in 0.01 M NaCl. The pitting potential and other electrochemical parameters suggested a combination of behaviors of both single-phase samples, suggesting that the global corrosion behavior may be represented by a composite theory applied to phases, their area fractions, and interphase length. However, the interphase in the dual-phase CCA was a local corrosion initiation site and may limit localized corrosion protectiveness. The alloy design implications for optimization of second phase structure and morphology are discussed.

A novel BCC-L21-BCC hierarchical heterostructure high entropy alloy with excellent corrosion resistance and mechanical properties in as-cast state

In this paper, a novel as-cast CrFeNiAl0.35Si0.1Ti0.1 high entropy alloy (HEA) with micron-to-nano hierarchical heterostructure was designed, and its microstructure, mechanical properties and corrosion resistance have been systematically investigated. It is found that, this novel HEA exhibits well-dispersed L21 phases with various sizes from micron-scale to nano-scale in the BCC matrix, while nano-sized BCC lamellas could also emerge in the L21 phase with large diameter. Moreover, this HEA exhibits not only excellent corrosion resistance in 3.5 wt.% NaCl solution that close to super-stainless steels, but also high mechanical properties combining yield strength of 1712±56 MPa, compressive plasticity of 21.2%±0.5% and hardness of ∼560 Hv. Such outstanding comprehensive properties for this HEA are possibly resulted from the complex hierarchical BCC-L21-BCC heterostructure with stable passive film and low diversity in work function between different phases. This work provides a novel route in the development of high-performance corrosion-resistant HEAs for structural and coating applications.

Enhancing mechanical and anti-corrosion properties in a L12 nanoprecipitates reinforced Fe35.4Ni24Cr21Co9Mo2Cu1.6Al3Ti4 multi-principal element alloy via tailoring grain size

A Fe35.4Ni24Cr21Co9Mo2Cu1.6Al3Ti4 multi-principal element alloy (MPEA) reinforced by L12 nanoprecipitates was fabricated with four different grain sizes (~19, ~50, ~127 and ~361 μm) to optimize mechanical and corrosion properties. All samples exhibit a similar microstructure, showing spherical L12 nanoprecipitates embedded in the FCC matrix at grain interiors, accompanied by a small fraction of plate-like L12 and B2-ordered phases at grain boundaries. As grain size decreases, both yield strength and ultimate tensile strength progressively increase, while ductility decreases. The sample with a grain size of ~50 μm demonstrates the most excellent combination of strength and ductility, displaying a yield strength of ~700MPa, an ultimate tensile strength of ~1130MPa, and a total elongation of ~29.4%. Concurrently, corrosion resistance in 3.5wt.% NaCl improves as grain size decreases from ~361 μm to ~50 μm, but notably deteriorates at ~19 μm. These results suggest that the L12 nanoprecipitates reinforced Fe35.4Ni24Cr21Co9Mo2Cu1.6Al3Ti4 MPEA with grain size of ~50 μm has achieved outstanding combination of mechanical and anti-corrosion properties. Precipitation strengthening and grain boundary strengthening are responsible for the enhanced mechanical properties in the studied samples. Electrochemical impedance spectroscopy (EIS) and X-ray photoelectron spectroscopy (XPS) revealed that the passive film on the ~50 μm grain size sample is the thickest (3.09nm), composed primarily of Cr2O3 and Fe2O3, which acts as an effective barrier against Cl- penetration. In a word, tailoring grain size proves to be an effective means to achieve enhanced mechanical and anti-corrosion properties.

Insight into the oxidation behavior and excellent internal oxidation and nitridation resistance of Fe71.5-x(Ni, Cr, Ti)28.5Alx complex concentrated alloys by advanced characterization

For precipitate-strengthened alloys, the decomposition of the precipitates at the subsurface during high-temperature oxidation is detrimental to mechanical properties. In this study, we adjusted Al concentrations in Fe71.5-x(Ni, Cr, Ti)28.5Alx (x = 8, 12, and 16 at. %) complex concentrated alloys (CCAs) to precipitate elongated cuboidal L21 with higher density and Al concentration, as well as reduced inter-precipitate spacing. This is more conducive to the rapid diffusion of Al to the matrix and grain boundaries, promoting the formation of a continuous and compact Al2O3 layer with random crystallographic orientation at 800 °C in air. This not only inhibits the further decomposition of the L21 phase but also avoids internal oxidation and nitridation.

A molecular dynamics study on mechanical performance and deformation mechanisms in nanotwinned NiCo-based alloys with nano-precipitates under high temperatures

Abstract Molecular dynamics simulations are performed to investigate the mechanical behavior of nanotwinned NiCo-based alloys containing coherent L12 nano-precipitates at different temperatures, as well as the interactions between the dislocations and nano-precipitates within the nanotwins. The simulation results demonstrate that both the yield stress and flow stress in the nanotwinned NiCo-based alloys with nano-precipitates decrease as the temperature rises, because the higher temperatures lead to the generation of more defects during yielding and lower dislocation density during plastic deformation. Moreover, the coherent L12 phase exhibits excellent thermal stability, which enables the hinderance of dislocation motion at elevated temperatures via the wrapping and cutting mechanisms of dislocations. The synergistic effect of nanotwins and nano-precipitates results in more significant strengthening behavior in the nanotwinned NiCo-based alloys under high temperatures. In addition, the high-temperature mechanical behavior of nanotwinned NiCo-based alloys with nano-precipitates is sensitive to the size and volume fraction of the microstructures. These findings could be helpful for the design of nanotwins and nano-precipitates to improve the high-temperature mechanical properties of NiCo-based alloys.

Microstructure and mechanical properties of an elevated temperature L12-type Ni-Co-Cr-Al-Ti-V-B-based high-entropy intermetallic

In this study, a novel L12-type Ni46.6Co23.3Cr10Al9Ti6V5B0.1 high-entropy intermetallic (HEI) with the excellent strength-ductility combination at 25 ℃ and 800 ℃ was prepared by vacuum arc melting. An ultrahigh volume fraction of cubical L12-type nanoparticles (~81%) was formed uniformly inside the grains after annealing. The intragranular L12 phase, FCC nanolayers, and intergranular blocky FCC precipitations constituted the heterogeneous structure. The annealed HEI exhibits high room-temperature yield strength (~711MPa) and ultimate tensile strength (~937MPa) with large tensile elongation (~17%). The room-temperature plasticity is superior to that of many other simple ordered intermetallics. The yield strength can still be maintained at ~740MPa with a total strain of about 6.7% when tested at 800°C, and its strength is higher than many L12 nanoparticle-strengthened high-entropy alloys. High strength is primarily attributed to the elevated volume fraction of L12 nanoparticles and the significant increase in the antiphase boundary energy caused by the addition of Ti and V elements. The stacking-fault (SF) networks, L-C locks, and K-W locks provide sustained work-hardening capacity, resulting in excellent yield strengths at 25 ℃ and 800 ℃. In addition, the favorable ductility is due to the formation of intragranular disordered FCC nanolayers and grain boundary FCC precipitations, which can avoid premature intergranular fracture.

Exceptional Strength-Ductility Combinations of a CoCrNi-Based Medium-Entropy Alloy via Short/Medium-Time Annealing after Hot-Rolling.

Strong yet ductile alloys have long been desired for industrial applications to enhance structural reliability. This work produced two (CoCrNi)93.5Al3Ti3C0.5 medium-entropy alloys with exceptional strength-ductility combinations, via short/medium (3 min/30 min) annealing times after hot-rolling. Three types of intergranular precipitates including MC, M23C6 carbides, and L12 phase were detected in both samples. Noticeably, the high-density of intragranular L12 precipitates were only found in the medium-time annealed sample. Upon inspection of the deformed substructure, it was revealed that the plane slip is the dominant deformation mechanism of both alloys. This is related to the lower stacking fault energy, higher lattice friction induced by the C solute, and slip-plane softening caused by intragranular dense L12 precipitates. Additionally, we noted that the stacking fault and twinning act as the mediated mechanisms in deformation of the short-time annealed alloy, while only the former mechanism was apparent in the medium-time annealed alloy. The inhibited twinning tendency can be attributed to the higher energy stacking faults and the increased critical twinning stress caused by intragranular dense L12 precipitates. Our present findings provide not only guidance for optimizing the mechanical properties of high/medium-entropy alloys, but also a fundamental understanding of deformation mechanisms.

Carbon-microalloying enhances strength-ductility synergy of (FeCoNi)90Al10 medium-entropy alloy via tailoring precipitation

The metastable high/medium-entropy alloys (H/MEAs) composing L12 nano-precipitates exhibit outstanding mechanical properties. In this work, the effect of carbon (C)-microalloying on the precipitation behavior and mechanical properties of (FeCoNi)90Al10 MEA was systematically investigated. With the addition of 0.2 at. % C, the yield strength of the alloy increased from 290.4 ± 1.3 MPa to 343.1 ± 2.8 MPa, the ultimate tensile strength increased from 648.5 ± 3.5 MPa to 686.1 ± 3.2 MPa, and the uniform elongation slightly increased after ageing for 45 min. C-microalloying resulted in a decrease of 0.85 kJ/mol and 0.26 kJ/mol in Gibbs free energy for face-centered cubic matrix to L12 and B2 phase transitions, facilitating the segregation of Al atom. This promoted the precipitation of L12 and B2 phases during ageing treatment, which enhanced ordering strengthening. The discontinuous precipitation was promoted at grain boundary after C-microalloying, providing an impetus for the movement of grain boundary. Meanwhile, the movement of grain boundary and the pinning of grain boundary by body-centered cubic precipitates resulted in the formation of grain boundary serration, which could release intergranular strain localization during deformation. Moreover, C-microalloying promoted the formation of planar slip and Taylor lattice during the deformation process, thus improving the plasticity. This finding provides a significant reference for C-microalloying and precipitate control of metastable MEAs.

Effect of Zn Addition on Phase Evolution in AlCrFeCoNiZn High‐Entropy Alloy

The addition of Zn to AlCrFeCoNi high‐entropy alloy (HEA) poses intriguing questions as to how it would affect phase evolution. Herein, the phase evolution in AlCrFeCoNiZn is studied using a combination of experimental techniques (X‐ray diffraction, scanning electron microscopy, energy‐dispersive spectroscopy, and differential scanning calorimetry) and computational (density‐functional theory [DFT], calculation of phase diagrams, and machine‐learning) methods. Mechanically alloyed and spark‐plasma‐sintered AlCrFeCoNiZn assumes a metastable single‐phase, body‐centered‐cubic (BCC) structure that undergoes diffusion‐controlled phase separation upon subsequent heat treatment to form separate (Al, Cr)‐rich, (Fe, Co)‐rich, and (Zn, Ni)‐rich phases. The formation of (Al, Cr)‐rich phase, not reported previously in AlCrFeCoNi‐based HEAs, is attributed to strong clustering tendency of Cr–Zn and Cr–Ni pairs, combined with the strong ordering of Zn–Ni pair, driving out Cr that in turn combines with Al to form a (Al, Cr)‐rich phase. In the DFT results, the formation of thermodynamically stable L12 phase is shown wherein Cr–Fe–Zn [Al–Ni‐Co] preferably occupy1a (000) [3c (0 ½ ½)] positions. The sluggish diffusional transformation to L12 phase from BCC precursors is attributed to the small stacking‐fault energy of AlCrFeCoNiZn. The equilibrated HEA exhibits a high microhardness of 8.24 GPa with an elastic modulus of 184 GPa.

Extending the Pre-ordered Precursor Reduction strategy to L10 ternary alloys: the case of MnFePt

L10 nanostructured alloys continue to attract a great deal of attention due to their advanced physico-chemical properties arising from the peculiar arrangement of the atoms in the tetragonal unit cell. Efforts have been focused on synthesizing and optimizing L10 3d-5d binary alloys, with the incorporation of a third element to enhance the chemical order degree and/or modulate the physical properties. Among the family members, magnetic L10 MnFePt ternary alloys are of great relevance owing to the possibility to tune the magnetic properties to meet the requirements of many applications including data storage/processing, sensors, catalysis, and biomedicine. In this work, a direct, effective and sustainable strategy, called Pre-ordered Precursor Reduction (PPR), was exploited for the first time to synthesize highly-ordered L10 MnFePt ternary alloy nanoparticles by thermal decomposition in reductive atmosphere of MnxFe1-x(H2O)6PtCl6 crystal salts whose crystallographic structure resembles the specific atomic arrangement of the L10 phase. Despite the higher complexity with respect to the binary system, the peculiar atomic arrangement of the elements in the precursor crystalline salt allows a great control over the structural and magnetic properties. By modulating the process conditions and the initial chemical composition it is possible to finely tune the magnetic properties thus proving the high versatility and efficiency of the PPR approach to synthesize highly ordered L10 ternary alloys with controlled properties.

Microstructure evolution and catalytic activity of AlCo1−xFeNiTiMox high entropy alloys fabricated by powder metallurgy route

This investigation presents the synthesis of equiatomic and non-equiatomic AlCo1−xFeNiTiMox (x = 0, 0.1, 0.25 and 1.0) high entropy alloys fabricated by mechanical alloying. Mo partially replaced Co. Classic thermodynamic calculations, such as mixing enthalpy (ΔHmix), configurational entropy (ΔSmix), the atomic size difference (δ), entropy to enthalpy ratio (Ω), electronegativity difference (△χ), and valence electron concentration (VEC) were used. Considering δ, Ω and VEC parameters, a BCC solid solution and an intermetallic phase can be predicted due to the partial replacement of Co by Mo. X-ray and electron diffraction of equiatomic HEA without Mo content revealed that after 35 h of milling, a Fe-type BCC lattice phase was formed in the alloy and two L21 phases, in addition to a minimal amount of FCC phase. As the Mo content increased, the Fe-type BCC phase was steadily replaced by the Mo-type BCC phase and the Fe-type FCC phase, and two L21 phases were also developed. When the 5 at% Mo-containing (x = 0.25) alloy was further milled for 80 h, the amount of phases remained almost the same; only the grain size was strongly reduced. The influence of the Mo addition on the properties of studied alloys was also confirmed in the decolourisation of Rhodamine B using a modified photo-Fenton process. The decolourisation efficiency within 20 min was 72% for AlCoFeNiTi and 87% for AlCo0.75FeNiTiMo0.25 using UV light with 365 nm wavelength.

Nanoindentation behaviors of the AlCoCrFeNi2.1 eutectic high-entropy alloy: The effects of crystal structures

The AlCoCrFeNi2.1 eutectic high-entropy alloy (EHEA), as a kind of in-situ composite materials, have achieved good match of strength and plasticity due to its typical eutectic lamella structures. Although many previous studies have investigated the indentation behaviors of the AlCoCrFeNi2.1 EHEA, there are still some controversies about the hardness characteristic of different crystal structures, requiring further clarification. Accordingly, in this study, nanoindentation tests were conducted to investigate the indentation behaviors of different crystal structures (primary L12 phase, primary B2 phase, and the eutectic phase region). The residual indentation and the crystallographic orientations were characterized by the laser scanning confocal microscope, scanning electron microscope, and electron backscatter diffraction. The hardness in different crystal structures were comparatively analyzed and the material deformation mechanisms were discussed correspondingly. The statistic results showed that the eutectic phase region had the lowest hardness, and primary B2 phase had the highest hardness. Furthermore, the slip lines in the primary L12 phase were evenly distributed near the residual indentation, but the slip lines in the eutectic phase region were concentrated near the phase boundaries. These findings are expected to deepen the understanding of the microscale deformation behaviors of EHEAs.

Tune Al/Ti to adjust FCC+L21 hetero-structured Ni-based high-entropy alloys for improved mechanical properties and wear resistance

Outstanding mechanical properties of Ni-based superalloy benefit from its coherent γ/γ’ structure via precipitation strengthening of γ matrix (FCC structure) by L12 Ni3Al-type γ’ phase. Back-stress strengthening is another effective strategy to further enhance the FCC+L12 structured Ni-based superalloy. In this work, we extend such approaches to high-entropy alloys (HEAs) by introducing different Al and Ti contents (5 at.% ∼18 at.%) into a Ni-based CrFe2Ni4 alloy to form FCC+L21 heterostructured AlxCrFe2Ni4Tiy HEAs. Detailed microstructural analysis indicates that L12 Ni3(Al,Ti)-type nanoparticles form in a (Ni,Fe,Cr)-rich FCC matrix. The volume fraction of L21 AlNi2Ti-type phase can be varied by adjusting the Al/Ti ratio and concentrations of Al and Ti. Higher Al and Ti contents promote L21 phase formation and higher Al/Ti ratio (>1) prohibits the high Ti-containing compounds such as D024η-Ni3Ti and C14 Laves Fe2Ti phases, which are hard but brittle. Corresponding Young's modulus, Poisson's ratio, hardness, and the bulk to shear modulus ratio (B/G) can be readily modified. Compressive tests demonstrate that Al1.5CrFe2Ni4Ti1.0 alloy with half FCC and half L21 phases possesses the optimal strength-ductility combination (with compressive yield strength of ∼1564 MPa and fracture strain of ∼28 %). DFT calculations were performed to elucidate relevant mechanisms. Sliding wear tests were also performed, which demonstrate superior wear resistance of the HEAs at both room and elevated temperatures, compared with a commercial Ni-based superalloy, UHT-Nickel.

Hierarchical ferrous medium entropy with heterogeneous precipitates embedded in core-shell grain structure for superior mechanical properties

Superalloys designed for high-temperature applications, featuring a face-centered cubic matrix and L12 precipitates, have shown excellent tensile properties at both room and elevated temperatures. However, the substantial Ni and Co, necessary for generating a high fraction of the ordered L12 phase within the matrix, results in high mass density and cost, subsequently limiting their widespread industrial application. It is important to increase Fe content over Ni and Co while preserving outstanding mechanical properties at ambient and high temperatures. In this study, we propose a novel approach to introduce a hierarchical structure in a 60-at%-Fe-based medium entropy alloy. The heterogeneous nano-precipitates embedded in harmonic (core-shell) grain structure reinforce mechanical contrast between soft and hard domains, achieving an excellent heterostructure. The present alloy incorporates hierarchical heterogeneity at multi-scales, combining heterogeneous grain at micrometers, precipitates at tens of nanometers, and elemental fluctuation at nanometers. This hierarchical structure shows superior mechanical properties at room and high temperatures comparable to those of conventional superalloys. Further, the high content of Fe in this alloy system shows excellent performance in alloy cost and mass density. This work suggests the unique hierarchical heterostructure to overcome the trade-off dilemma in alloy cost, mass density, and mechanical properties in room/elevated temperatures.

Complex precipitation behavior in a Co-free high entropy alloy during aging

High entropy alloys (HEAs) demonstrate high strength, thermal stability, and irradiation resistance, making them desirable for applications in nuclear reactors and other harsh environments. Many existing HEAs contain cobalt (Co), which makes them unsuitable for nuclear applications due to the long-term activation of Co. A previously studied Co-free alloy, (Fe0.3Ni0.3Mn0.3Cr0.1)88Ti4Al8, exhibits high strength but compromised ductility due to its network of brittle precipitates upon aging. This work investigates the formation mechanism and evolution of the precipitates, including L12 (Ni3Ti type, ordered face-centered cubic structure), B2 (NiAl type, ordered body-centered cubic structure), and Chi (FeCr-rich ordered α-Mn structure), in this alloy at 650 °C, the aging temperature that yields the alloy’s peak strength after 120 hours. Using ex-situ scanning electron microscopy, transmission electron microscopy, and atom probe tomography, the precipitates were characterized in terms of their composition, morphology, and crystal structure at various aging times. In addition, synchrotron-based, in-situ X-ray diffraction was used to probe the evolution of precipitates in the bulk during key phases of in-situ aging. The L12 precipitates exhibit complex growth and coarsening behavior – their coarsening starts after just 24 hours, and competition between the L12 and B2 phases arises after 72 hours leading to a decrease in L12 volume fraction. Conversely, B2 and Chi precipitates exhibit delayed nucleation and growth, and do not form in observable quantities until after 24 hours. Once formed, however, these precipitates quickly dominate the microstructure, with >50 % volume fraction after 120 hours, leading to the previously observed mechanical properties. This study provides a foundational understanding of the evolution of multi-precipitate structures in HEAs and guides future alloy development and optimization by tailoring the precipitates.

Investigation on the structural, elastic, electronic, thermodynamic, and vibrational properties of the full heusler Sc2XAl (X =Cd and Zn): An ab initio study

The structural, mechanical, electronic, thermodynamic, and phonon characteristics of Sc2CdAl and Sc2ZnAl in L21 phase were the main focuses on this investigation. The density of states (DOS) and electronic band spectra signify the metallic behavior of the L21 phase of both materials. The impact of atomic arrangement with respect to the Wyckoff sites on the mechanical stability were additionally studied. The elastic constants of Sc2CdAl and Sc2ZnAl alloys indicated that these alloys convened Born mechanical stability criteria. Using the density functional perturbation theory's first-principle linear response method, complete phonon spectra have been acquired. Moreover, the quasi-harmonic approximation, specific heat capacity at constant volume, the internal free energy, entropy, and vibrational free energy variations of Sc2CdAl and Sc2ZnAl as full Heusler alloys have been utilized in examination the change over the temperature between 0 and 800 K. Both alloys might find application in real industrial applications.

Enhancing oxidation resistance via grain boundary engineering in L12-strengthened medium entropy alloys

The concept of grain boundary engineering (GBE) has been successfully applied to L12-strengthened (CoCrNi)94Al3Ti3 medium entropy alloy, with the aim of improving the oxidation resistance by increasing the ratio of special boundaries and suppressing discontinuous precipitation. Surprisingly, our results reveal that GBE treatment not only slows down the oxidation kinetics and but also alters the oxide scale from TiO2 and multi-defect Cr2O3 to continuous and protective Cr2O3 and Al2O3, thereby contributing to an enhanced oxidation and anti-spalling resistance. The GBE treatment reduces the oxidation weight gain of the current alloy from 1.950 mg cm–2 to 1.211 mg cm–2 after 100 h of cyclic oxidation at 800 °C. The findings show that the extensive outward diffusion of Ti accelerates ion transport and promotes microporosity, thus leading to more defects being formed in the oxide film. The GBE treatment suppresses the discontinuous precipitation of the Ti-bearing L12 phase and breaks the random large angular grain boundaries network, inhibiting the diffusion of Ti and ultimately enhancing the oxidation properties of the alloy. The current work provides an idea of oxidation resistance enhancement for Ti-bearing L12-strengthened alloys without changing the alloy composition.

Effect of heat treatment on microstructure and mechanical properties of lightweight high-entropy alloy

High-performance lightweight materials are in demand for a wide range of critical applications in the automotive, aviation, and aerospace industries. However, it remains difficult to enhance the strength of these alloys without significantly reducing their tensile ductility. Here, using different heat treatment routes, we overcome this inherent strength and ductility trade-off dilemma by introducing low lattice misfit precipitates in a lightweight high-entropy alloy (LHEA). In particular, the A700 alloy exhibits a high yield strength of 609 MPa and a tensile ductility of ∼24 % at room temperature, benefitting from the highly dispersed, low lattice misfit L12 and nano-lamellar body-centered cubic (BCC) phases.