Synthesis and Ultrahigh Pressure Compression of High-Entropy Boride (Hf0.2Mo0.2Nb0.2Ta0.2Zr0.2)B2 to 220 GPa

The high-entropy boride (Hf_0.2Mo_0.2Nb_0.2Ta_0.2Zr_0.2)B₂ material was synthesized under high-pressures and high-temperatures in a large-volume Paris-Edinburgh (PE) press from a ball-milled powder mix of HfO₂, MoO₃, Nb₂O_5, Ta₂O₅, ZrO₂, carbon black, and boron carbide. The transformation process was monitored in situ by energy-dispersive x-ray diffraction with conversion starting at 1100 °C and completed by 2000 °C with the formation of a single hexagonal AlB₂-type phase. The synthesized sample was recovered, powdered, and mixed with platinum pressure marker and studied under high pressure by angle-dispersive x-ray diffraction in a diamond anvil cell. The hexagonal AlB₂-type phase of (Hf_0.2Mo_0.2Nb_0.2Ta_0.2Zr_0.2)B₂ was found to be stable up to the highest pressure of 220 GPa reached in this study (volume compression V/V₀ = 0.70). The third order Birch-Murnaghan equation of state fit to the high-pressure data up to 220 GPa results in an ambient pressure unit cell volume V0=28.16±0.04 Å3, bulkmodulus Ko = 407 ± 6 GPa, pressure derivative of bulk-modulus K0′ = 2.73 ± 0.045 GPa. Our study indicates that this high-entropy boride (Hf_0.2Mo_0.2Nb_0.2Ta_0.2Zr_0.2)B₂ material is stable to ultrahigh pressures and temperatures and exhibit high bulk modulus similar to other incompressible transition metal borides like ReB₂ and Os₂B₃.     

Phase Transformation Induced by High Pressure Torsion in the High-Entropy Alloy CrMnFeCoNi

The forward and reverse phase transformation from face-centered cubic (fcc) to hexagonal close-packed (hcp) in the equiatomic high-entropy alloy (HEA) CrMnFeCoNi has been investigated with diffraction of high-energy synchrotron radiation. The forward transformation has been induced by high pressure torsion at room and liquid nitrogen temperature by applying different hydrostatic pressures and large shear strains. The volume fraction of hcp phase has been determined by Rietveld analysis after pressure release and heating-up to room temperature as a function of hydrostatic pressure. It increases with pressure and decreasing temperature. Depending on temperature, a certain pressure is necessary to induce the phase transformation. In addition, the onset pressure depends on hydrostaticity; it is lowered by shear stresses. The reverse transformation evolves over a long period of time at ambient conditions due to the destabilization of the hcp phase. The effect of the phase transformation on the microstructure and texture development and corresponding microhardness of the HEA at room temperature is demonstrated. The phase transformation leads to an inhomogeneous microstructure, weakening of the shear texture, and a surprising hardness anomaly. Reasons for the hardness anomaly are discussed in detail.     

Corrosion Behavior of the AlCoCrFeNi2.1 Eutectic High-Entropy Alloy in Chloride-Containing Sulfuric Acid Solutions at Different Temperatures

In this work, the influence of temperature on the corrosion behavior of AlCoCrFeN_i2.1 eutectic high-entropy alloy in a chloride-containing sulfuric acid solution was investigated using electrochemical measurement, X-ray photoelectron spectroscopy, and scanning electron microscopy. Results show that the passive film of AlCoCrFeN_i2.1 is stable in chloride-containing sulfuric acid solutions at low temperatures, while an unstable film forms on the alloy at high temperatures. Furthermore, temperature changes the proportion of hydroxide and oxide in Fe and Cr, but it has no noticeable effect on Al and Ni, which is a significant factor on the passive behavior. L12 phase exhibits good corrosion resistance at different temperatures. Pitting occurred on B2 phase in the chloride-containing sulfuric acid solution at a low temperature of 5 °C, while pitting and dissolution take place on AlCoCrFeNi_2.1 in the acid solution at room temperature and above.     

Effects of W Alloying on the Lattice Distortion and Wear Behavior of Laser Cladding AlCoCrFeNiWx High-Entropy Alloy Coatings

Friction and wear properties of hot working die steel at above 800 °C are of particular interest for high temperature applications. Here, novel AlCoCrFeNiW_x high-entropy alloy (HEA) coatings have been fabricated on the surface of hot working die steel by laser cladding. The effects of the as-prepared AlCoCrFeNiW_x HEA coatings on the microstructure and high temperature friction and wear behavior of hot working die steel are investigated through scanning electron microscopy (SEM), electron probe microanalysis (EPMA), X-ray diffraction (XRD), and X-ray absorption fine structure (XAFS). Having benefited from the formation of W-rich intermetallic compounds after the addition of W elements, the high temperature wear resistance of the coatings is obviously improved, and friction coefficient shows a large fluctuation. The microstructural characteristics of the AlCoCrFeNiW_x HEA coatings after the high temperature wear resistance test shows a highly favorable impact on microstructure stability and wear resistance, due to its the strong lattice distortion effect of W element on BCC solid solutions and the second phase strengthening of the W-rich intermetallic compounds. These findings may provide a method to design the high temperature wear resistant coatings.     

Machine Learning-Based Strength Prediction for Refractory High-Entropy Alloys of the Al-Cr-Nb-Ti-V-Zr System

The aim of this work was to provide a guidance to the prediction and design of high-entropy alloys with good performance. New promising compositions of refractory high-entropy alloys with the desired phase composition and mechanical properties (yield strength) have been predicted using a combination of machine learning, phenomenological rules and CALPHAD modeling. The yield strength prediction in a wide range of temperatures (20–800 °C) was made using a surrogate model based on a support-vector machine algorithm. The yield strength at 20 °C and 600 °C was predicted quite precisely (the average prediction error was 11% and 13.5%, respectively) with a decrease in the precision to slightly higher than 20% at 800 °C. An Al₁₃Cr₁₂Nb₂₀Ti₂₀V₃₅ alloy with an excellent combination of ductility and yield strength at 20 °C (16.6% and 1295 MPa, respectively) and at 800 °C (more 50% and 898 MPa, respectively) was produced based on the prediction.     

Corrosion Behavior of Ultrafine-Grained CoCrFeMnNi High-Entropy Alloys Fabricated by High-Pressure Torsion

The influence of the nanocrystalline structure produced by severe plastic deformation (SPD) on the corrosion behavior of CoCrFeMnNi alloys with Cr contents ranging from 0 to 20 at.% was investigated in aqueous 0.5 M H₂SO₄ and 3.5% NaCl solutions. The resistance to general corrosion and pitting became higher in both the solutions, with higher passivation capability observed with increasing Cr content, and it is believed that the high corrosion resistance of CoCrFeMnNi alloys can be attributed to the incorporation of the Cr element. However, the impact of the nanocrystalline structure produced by SPD on the corrosion behavior was negligibly small. This is inconsistent with reports on nanocrystalline binary Fe–Cr alloys and stainless steels processed by SPD, where grain refinement by SPD results in higher corrosion resistance. The small change in the corrosion behavior with respect to grain refinement is discussed, based on the passivation process of Fe–Cr alloys and on the influence of the core effects of HEAs on the passivation process.     

Tribological Properties of High-Entropy Alloys under Dry Conditions for a Wide Temperature Range—A Review

High-entropy alloys (HEAs) are composed of multiple elements with equimolar or near equimolar composition that have superior mechanical and tribological properties. In this article, we present a review on the tribological performance of HEAs. The tribological properties of different HEAs systems have been evaluated, and it has been found that the wear rate strongly depends on the crystal structure of the phases. The most common structures are face-centered cubic (FCC), body-centered cubic (BCC), and dual-phase (FCC + BCC) alloys due to the high entropy of mixing instead of forming intermetallic phases. In general, HEAs with a BCC structure showed superior hardness and wear properties compared to FCC and FCC + BCC alloys. The lesser wear rate of HEAs with a BCC structure is attributed to the reductions in ductility, resulting in strong but brittle alloys. In addition to the crystal structure, the effect of temperature on the tribological performance of the HEAs is also discussed, which highlights their potential applications for high temperatures. Moreover, various other factors such as grain size, formation of an oxide layer, and wear mechanisms are discussed.     

Behavior of Biochar-Modified Cementitious Composites Exposed to High Temperatures

In this study, the effect of biochar on the high temperature resistance of cementitious paste was investigated using multiple experimental methods. The weight loss, cracks, residual compressive strength, and ultrasonic pulse velocity (UPV) of biochar cementitious paste with 2% and 5% biochar exposed to 300, 550 and 900 °C were measured. The products and microstructures of biochar cementitious paste exposed to high temperatures were analyzed by X-ray diffraction, Fourier transform infrared spectroscopy, thermogravimetric analysis, and scanning electron microscopy. The results showed that the cracks of specimens exposed to high temperatures decreased with increasing biochar content. The addition of 2% and 5% biochar increased the residual compressive strength of the specimens exposed to 300 °C and the relative residual compressive strength at 550 °C. As the exposure temperature increased, the addition of biochar compensated for the decreasing ultrasonic pulse velocity. The addition of biochar contributed to the release of free water and bound water, and reduced the vapor pressure of the specimen. The addition of biochar did not change the types of functional groups and crystalline phases of the products of cementitious materials exposed to high temperatures. Biochar particles were difficult to observe at 900 °C in scanning electron microscopy images. In summary, because biochar has internal pores, it can improve the high-temperature resistance of cement paste.     

Effect of Si and B on the Electrochemical Behavior of FeCoNiCr-Based High-Entropy Amorphous Alloys

The ability to produce high-entropy alloys with an amorphous structure, so-called high-entropy metallic glasses (HEMGs), offers the possibility to produce new compositions with good mechanical properties and resistance to corrosion. In this study, corrosion behavior was studied in two HEMGs, FeCoNiCrB and FeCoNiCr(BSi). In both cases, the total amount of metalloid atoms was kept constant at 20 at.%. The electrochemical behavior of these alloys was studied by means of linear polarization resistance (LPR) measurements and electrochemical impedance spectroscopy in a 3 wt.% NaCl solution. The effect of corrosion was characterized by using X-ray photoelectron spectroscopy (XPS) and the surface morphology was checked using a scanning electron microscope (SEM). The results show that samples with B but without Si exhibit better corrosion resistance due to its chemical homogeneity and lack of structural heterogeneity.     

Study on Durability and Pore Characteristics of Concrete under Salt Freezing Environment

The macroscopic mechanical properties and frost resistance durability of concrete are closely related to the changes in the internal pore structure. In this study, the two-dimensional and three-dimensional ICT (Industrial Computerized Tomography) pore characteristics of C30 concrete specimens before and after freezing and thawing in clean water, 5 wt.% NaCl, 5 wt.% CaCl₂, and 5 wt.% CH₃COOK solution environments are obtained through concrete frost resistance durability test and ICT scanning technology. The effects of pore structure changes on concrete frost resistance, durability, and compressive strength mechanical properties after freezing and thawing cycles in different salt solution environments are analyzed. This paper provides new means and ideas for the study of concrete pores. The results show that with the increase in the freezing and thawing times, the concrete porosity, two-dimensional pore area, three-dimensional pore volume, and pore number generally increase in any solution environment, resulting in the loss of concrete compressive strength, mortar spalling, and the decrease in the relative dynamic elastic modulus. Among them, the CH₃COOK solution has the least influence on the concrete pore changes; the NaCl solution has the greatest influence on the change in the concrete internal porosity. The damage of CaCl₂ solution to concrete is second only to the NaCl solution, followed by clean water. The increase in the concrete internal porosity from high to low is NaCl, CaCl₂, clean water, and CH₃COOK. The change in the pore volume of 0.1 to 1 mm³ after the freeze–thaw cycle is the main factor for reducing concrete strength. The test results have certain guiding value for the selection of deicing salt in engineering.     

Study on Mechanical Properties of Basalt Fiber Shotcrete in High Geothermal Environment

With the development of infrastructure, there are growing numbers of high geothermal environments, which, therefore, form a serious threat to tunnel structures. However, research on the changes in mechanical properties of shotcrete under high temperatures and humid environments are insufficient. In this paper, the combination of various temperatures (20 °C/40 °C/60 °C) and 55% relative humidity is used to simulate the effect of environment on the strength and stress–strain curve of basalt fiber reinforced shotcrete. Moreover, a constitutive model of shotcrete considering the effect of fiber content and temperature is established. The results show that the early mechanical properties of BFRS are improved with the increase in curing temperature, while the compressive strength at a later age decreases slightly. The 1-day and 7-day compressive strength of shotcrete at 40 °C and 60 °C increased by 10.5%, 41.1% and 24.1%, 66.8%, respectively. The addition of basalt fiber can reduce the loss of later strength, especially for flexural strength, with a increase rate of 11.9% to 39.5%. In addition, the brittleness of shotcrete increases during high temperature curing, so more transverse cracks are observed in the failure mode, and the peak stress and peak strain decrease. The addition of basalt fiber can improve the ductility and plasticity of shotcrete and increase the peak strain of shotcrete. The constitutive model is in good agreement with the experimental results.     

Microstructure and Thermal Analysis of Metastable Intermetallic Phases in High-Entropy Alloy CoCrFeMo0.85Ni

CoCrFeMoNi high entropy alloys (HEAs) exhibit several promising characteristics for potential applications of high temperature coating. In this study, metastable intermetallic phases and their thermal stability of high-entropy alloy CoCrFeMo_0.85Ni were investigated via thermal and microstructural analyses. Solidus and liquidus temperatures of CoCrFeMo_0.85Ni were determined by differential thermal analysis as 1323 °C and 1331 °C, respectively. Phase transitions also occur at 800 °C and 1212 °C during heating. Microstructure of alloy exhibits a single-phase face-centred cubic (FCC) matrix embedded with the mixture of (Co, Cr, Fe)-rich tetragonal phase and Mo-rich rhombohedron-like phase. The morphologies of two intermetallics show matrix-based tetragonal phases bordered by Mo-rich rhombohedral precipitates around their perimeter. The experimental results presented in our paper provide key information on the microstructure and thermal stability of our alloy, which will assist in the development of similar thermal spray HEA coatings.     

A Literature Review of Concrete Ability to Sustain Strength after Fire Exposure Based on the Heat Accumulation Factor

Concrete is susceptible to damage during and after high-temperature exposure (most frequently in fire). The concrete partial strength re-gain after a high-temperature exposure obtained by the rehydration process is undoubtedly an advantage of this construction material. However, to use fire-damaged concrete, one has to know why the strength deteriorates and what makes the partial re-gain. Within this framework, the paper aims to find what factors influence the strength re-gain. Moreover, an attempt is made to introduce a measure collecting various influences such as the modified heat accumulation factor—accounting only for that which is important for the process, the temperature decomposing cement paste (i.e., above 400 °C). Several factors, i.e., peak temperature, heating time and rate, cooling regime, post-fire re-curing, concrete composition, age of concrete at exposure, porosity, load level at exposure, and heat accumulation are presented by their influence on the relative residual compressive strength, i.e., a portion of initial strength that is obtained after temperature exposure and strength re-gain. Since the relative strength unifies various concretes, a more general assessment and discussion are presented based on the experimental results and correlation factors. As fundamental influences determining the residual strength, the heating time, peak temperature, cooling, or post-heating re-curing regimes are found with the load level at exposure being inadequately examined. This paper also shows the superiority of the modified heat accumulation factor, but the results obtained are not satisfactory, and additional experimental data are necessary to develop a theoretical model of the residual strength.     

Microstructure and Magnetic Field-Induced Strain of a Ni-Mn-Ga-Co-Gd High-Entropy Alloy

The effect of a high-entropy design on martensitic transformation and magnetic field-induced strain has been investigated in the present study for Ni-Mn-Ga-Co-Gd ferromagnetic shape-memory alloys. The purpose was to increase the martensitic transition temperature, as well as the magnetic field-induced strain, of these materials. The results show that there is a co-existence of β, γ, and martensite phases in the microstructure of the alloy samples. Additionally, the martensitic transformation temperature shows a markedly increasing trend for these high-entropy samples, with the largest value being approximately 500 °C. The morphology of the martensite exhibits typical twin characteristics of type L1₀. Moreover, the magnetic field-induced strain shows an increasing trend, which is caused by the driving force of the twin martensite re-arrangement strengthening.     

The Effect of Scandium on the Structure,Microstructure and Superconductivity of Equimolar Sc-Hf-Nb-Ta-Ti-Zr Refractory High-Entropy Alloys

In this study, we investigate the scandium-containing Sc-Hf-Nb-Ta-Ti-Zr system of refractory high-entropy alloys (HEAs). Using the arc-melting method, we synthesized nine equimolar alloys (five 4-, three 5- and one 6-component), with all of them containing Sc. The alloys were characterized by XRD, electron microscopy and EDS, while superconductivity was investigated via electrical resistivity, specific heat and the Meissner effect. The results were compared to the parent Hf-Nb-Ta-Ti-Zr refractory HEAs, forming a single-phase body-centered cubic (bcc) structure and quite homogeneous microstructure. The addition of Sc produces a two-phase structure in the Sc-Hf-Nb-Ta-Ti-Zr alloys, with one phase being bcc and the other hexagonal close-packed (hcp). The hcp phase absorbs practically all Sc, whereas the Sc-poor bcc phase is identical to the bcc phase in the Hf-Nb-Ta-Ti-Zr parent system. Upon the Sc addition, the microstructure becomes very inhomogeneous. Large bcc dendrites (10–100 µm) are homogeneous in the central parts, but become a fine dispersion of sub-micron precipitates of the bcc and hcp phases close to the edges. The interdendritic regions are also a fine dispersion of the two phases. Superconductivity of the Sc-Hf-Nb-Ta-Ti-Zr alloys originates from the bcc phase fraction, which demonstrates identical superconducting parameters as the bcc Hf-Nb-Ta-Ti-Zr parent alloys, while the Sc-containing hcp phase fraction is non-superconducting.     

Microstructure and Corrosive Wear Properties of CoCrFeNiMn High-Entropy Alloy Coatings

In order to improve the wear resistance of offshore drilling equipment, CoCrFeNiMn high-entropy alloy coatings were prepared by cold spraying (CS) and high-speed oxygen fuel spraying (HVOF), and the coatings were subjected to vacuum heat treatment at different temperatures (500 °C, 700 °C and 900 °C). The friction and wear experiments of the coatings before and after vacuum heat treatment were carried out in simulated seawater drilling fluid. The results show that CoCrFeNiMn high-entropy alloy coatings prepared by CS and HVOF have dense structure and bond well with the substrate. After vacuum heat treatment, the main peaks of all oriented FCC phases are broadened and the peak strength is obviously enhanced. The two types of coatings achieve maximum hardness after vacuum heat treatment at 500 °C; the Vickers microhardness of CS-500 °C and HVOF-500 °C are 487.6 and 352.4 HV_0.1, respectively. The wear rates of the two coatings at room temperature are very close. CS and HVOF coatings both have the lowest wear rate after vacuum heat treatment at 500 °C. The CS-500 °C coating has the lowest wear rate of 0.2152 mm³ m⁻¹ N⁻¹, about 4/5 (0.2651 mm³ m⁻¹ N⁻¹) of the HVOF-500 °C coating. The wear rates and wear amounts of the two coatings heat-treated at 700 °C and 900 °C decrease due to the decrease in microhardness. The wear mechanisms of the coatings before and after vacuum heat treatment are adhesive wear, abrasive wear, fatigue wear and oxidation wear.     

Microstructure and Mechanical Properties of Co32Cr28Ni32.94Al4.06Ti3 High-Entropy Alloy

High-entropy alloys have good application prospects in nuclear power plants due to their excellent mechanical properties and radiation resistance. In this paper, the microstructure of the Co₃₂Cr₂₈Ni₃₂.₉₄Al₄.₀₆Ti₃ high-entropy alloy was researched using metallurgical microscopy, X-ray diffraction, and scanning electron microscopy. The mechanical properties were tested using a Vickers microhardness tester and a tensile testing machine, respectively. The results showed that Co₃₂Cr₂₈Ni₃₂.₉₄Al₄.₀₆Ti₃ had a single-phase, disordered, face-centered, cubic solid-solution structure and was strengthened by solid solution. The alloy lattice parameter and density were estimated as 0.304 nm and 7.89 g/cm³, respectively. The test results indicated that the alloy had satisfactory mechanical properties with yield stress and tensile strength of about 530 MPa and 985 MPa, respectively.     

Synthesis and Properties of the Gallium-Containing Ruddlesden-Popper Oxides with High-Entropy B-Site Arrangement

For the first time, the possibility of obtaining B-site disordered, Ruddlesden–Popper type, high-entropy oxides has been proven, using as an example the LnSr(Co,Fe,Ga,Mn,Ni)O₄ series (Ln = La, Pr, Nd, Sm, or Gd). The materials were synthesized using the Pechini method, followed by sintering at a temperature of 1200 °C. The XRD analysis indicated the single-phase, I4/mmm structure of the Pr-, Nd-, and Sm-based materials, with a minor content of secondary phase precipitates in La- and Gd-based materials. The SEM + EDX analysis confirms the homogeneity of the studied samples. Based on the oxygen non-stoichiometry measurements, the general formula of LnSr(Co,Fe,Ga,Mn,Ni)O_4+δ, is established, with the content of oxygen interstitials being surprisingly similar across the series. The temperature dependence of the total conductivity is similar for all materials, with the highest conductivity value of 4.28 S/cm being reported for the Sm-based composition. The thermal expansion coefficient is, again, almost identical across the series, with the values varying between 14.6 and 15.2 × 10⁻⁶ K⁻¹. The temperature stability of the selected materials is verified using the in situ high-temperature XRD. The results indicate a smaller impact of the lanthanide cation type on the properties than has typically been reported for conventional Ruddlesden–Popper type oxides, which may result from the high-entropy arrangement of the B-site cations.     

Microstructure and Friction Properties of CoCrFeMnNiTix High-Entropy Alloy Coating by Laser Cladding

To enhance the friction and wear properties of 40Cr steel’s surface, CoCrFeMnNi high-entropy alloy (HEA) coatings with various Ti contents were prepared using laser cladding. X-ray diffraction (XRD), scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) were used to characterize the phase composition, microstructure, and chemical composition of the samples. The findings demonstrated that the CoCrFeMnNiTi_x HEA coatings formed a single FCC phase. Fe₂Ti, Ni₃Ti, and Co₂Ti intermetallic compounds were discovered in the coatings when the molar ratio of Ti content was greater than 0.5. The EDS findings indicated that Cr and Co/Ni/Ti were primarily enriched in the dendrite and interdendrite, respectively. Ti addition can effectively enhance the coating’s mechanical properties. The hardness test findings showed that when the molar ratio of Ti was 0.75, the coating’s microhardness was 511 HV0.5, which was 1.9 times the hardness of the 40Cr (256 HV0.5) substrate and 1.46 times the hardness of the CrCrFeMnNi HEA coating (348 HV0.5). The friction and wear findings demonstrated that the addition of Ti can substantially reduce the coating’s friction coefficient and wear rate. The coating’s wear resistance was the best when the molar ratio of Ti was 0.75, the friction coefficient was 0.296, and the wear amount was 0.001 g. SEM and 3D morphology test results demonstrated that the coating’s wear mechanism changed from adhesive wear and abrasive wear to fatigue wear and abrasive wear with the increase in Ti content.     

Lithium-Ion Batteries under Low-Temperature Environment: Challenges and Prospects

Lithium-ion batteries (LIBs) are at the forefront of energy storage and highly demanded in consumer electronics due to their high energy density, long battery life, and great flexibility. However, LIBs usually suffer from obvious capacity reduction, security problems, and a sharp decline in cycle life under low temperatures, especially below 0 °C, which can be mainly ascribed to the decrease in Li⁺ diffusion coefficient in both electrodes and electrolyte, poor transfer kinetics on the interphase, high Li⁺ desolvation barrier in the electrolyte, and severe Li plating and dendrite. Targeting such issues, approaches to improve the kinetics and stability of cathodes are also dissected, followed by the evaluation of the application prospects and modifications between various anodes and the strategies of electrolyte design including cosolvent, blended Li salts, high-concentration electrolyte, and additive introduction. Such designs elucidate the successful exploration of low-temperature LIBs with high energy density and long lifespan. This review prospects the future paths of research for LIBs under cold environments, aiming to provide insightful guidance for the reasonable design of LIBs under low temperature, accelerating their widespread application and commercialization.