High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical ...High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical strength,and outstanding catalytic activity.These distinctive characteristics render HEMs highly suitable for various battery components,such as electrodes,electrolytes,and catalysts.This review systematically examines recent advances in the application of HEMs for energy storage,beginning with fundamental concepts,historical development,and key definitions.Three principal categories of HEMs,namely high-entropy alloys,high-entropy oxides,and highentropy MXenes,are analyzed with a focus on electrochemical performance metrics such as specific capacity,energy density,cycling stability,and rate capability.The underlying mechanisms by which these materials enhance battery performance are elucidated in the discussion.Furthermore,the pivotal role of machine learning in accelerating the discovery and optimization of novel high-entropy battery materials is highlighted.The review concludes by outlining future research directions and potential breakthroughs in HEM-based battery technologies.展开更多
Electroosmotic transport and entropy generation play a decisive role in regulating efficiency,stability,and energy cost of non-Newtonian nanoblood flows in stenosed arteries,particularly with tapered geometries.Thisst...Electroosmotic transport and entropy generation play a decisive role in regulating efficiency,stability,and energy cost of non-Newtonian nanoblood flows in stenosed arteries,particularly with tapered geometries.Thisstudy develops a unified model to analyze ZnO-Williamson nanoblood flow through a stenosed artery with converging,diverging,and non-tapered configurations,incorporating electroosmosis,viscous dissipation,and entropy production.The arterial walls are assumed to be electrically charged with a no-slip condition to induce electroosmotic propulsionalong the endothelial surface.The partial differential equations are nondimensionalized to a coupled system ofnonlinear ordinary differential equations,which are solved numerically using a MATLAB-based shooting technique.Parametric investigation is conducted for Brinkman,Grashof,and Weissenberg numbers,ZnO fractional volume,volumetric flow rate,and Helmholtz-Smoluchowski velocity to quantify their influences on axial velocity,wall shearstress,impedance resistance,temperature distribution,entropy generation,Bejan number,and streamline topology.The axial velocity decreases radially with increasing Brinkman number for all arterial geometries.Increasing ZnOnanoparticles improves thermal transport owing to enhanced effective thermal conductivity but simultaneously elevatesentropy generation due to increased viscous dissipation.Higher Weissenberg numbers suppress entropy production bypromoting elastic stress redistribution and lowering shear-induced irreversibility.Impedance resistance decreases withincreasing stenosis height but increases with stenosis shape parameter and ZnO fractional volume.Streamline analysisshows that buoyancy and viscoelasticity significantly distort flow near the stenosis,while increasing electroosmoticvelocity stabilizes streamlines,suppresses recirculation,and reduces local shear stress and pressure fluctuations.Inconclusion,electroosmotic actuation is most effective in reducing flow resistance in the converging tapered artery,particularly at lower ZnO volume fractions.Overall,the findings highlight the potential of optimized electroosmoticactuation and controlled nanoparticle loading to minimize thermodynamic losses,regulate shear stress,and improveflow uniformity in stenosed vessels,with promising implications for electro-assisted drug delivery,nanotherapeutics,and bio-inspired vascular microfluidic systems.展开更多
High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic f...High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic features enable forming-free resistive switching,multilevel conductance modulation,and synaptic plasticity,making HEOs attractive for neuromorphic computing.This review outlines recent progress in HEO-based memristors across materials engineering,switching mechanisms,and synaptic emulation.Particular attention is given to vacancy migration,phase transitions,and valence-state dynamics—mechanisms that underlie the switching behaviors observed in both amorphous and crystalline systems.Their relevance to neuromorphic functions such as short-term plasticity and spike-timing-dependent learning is also examined.While encouraging results have been achieved at the device level,challenges remain in conductance precision,variability control,and scalable integration.Addressing these demands a concerted effort across materials design,interface optimization,and task-aware modeling.With such integration,HEO memristors offer a compelling pathway toward energy-efficient and adaptable brain-inspired electronics.展开更多
(NbZrHfTi)C high-entropy ceramics,as an emerging class of ultra-high-temperature materials,have garnered significant interest due to their unique multi-principal-element crystal structure and exceptional hightemperatu...(NbZrHfTi)C high-entropy ceramics,as an emerging class of ultra-high-temperature materials,have garnered significant interest due to their unique multi-principal-element crystal structure and exceptional hightemperature properties.This study systematically investigates the mechanical properties of(NbZrHfTi)C high-entropy ceramics by employing first-principles density functional theory,combined with the Debye-Grüneisen model,to explore the variations in their thermophysical properties with temperature(0–2000 K)and pressure(0–30 GPa).Thermodynamically,the calculated mixing enthalpy and Gibbs free energy confirm the feasibility of forming a stable single-phase solid solution in(NbZrHfTi)C.The calculated results of the elastic stiffness constant indicate that the material meets the mechanical stability criteria of the cubic crystal system,further confirming the structural stability.Through evaluation of key mechanical parameters—bulk modulus,shear modulus,Young’s modulus,and Poisson’s ratio—we provide comprehensive insight into the macro-mechanical behaviour of the material and its correlation with the underlying microstructure.Notably,compared to traditional binary carbides and their average properties,(NbZrHfTi)C exhibits higher Vickers hardness(Approximately 28.5 GPa)and fracture toughness(Approximately 3.4 MPa⋅m^(1/2)),which can be primarily attributed to the lattice distortion and solid-solution strengthening mechanism.The study also utilizes the quasi-harmonic approximation method to predict the material’s thermophysical properties,including Debye temperature(initial value around 563 K),thermal expansion coefficient(approximately 8.9×10^(−6) K−1 at 2000 K),and other key parameters such as heat capacity at constant volume.The results show that within the studied pressure and temperature ranges,(NbZrHfTi)C consistently maintains a stable phase structure and good thermomechanical properties.The thermal expansion coefficient increasing with temperature,while heat capacity approaches the Dulong-Petit limit at elevated temperatures.These findings underscore the potential of(NbZrHfTi)C applications in ultra-high temperature thermal protection systems,cutting tool coatings,and nuclear structural materials.展开更多
High-entropy magnetocaloric alloys offer exceptional compositional flexibility and stability for magnetic refrigeration.However,enhancing their magnetic entropy change,working temperature range,and refrigeration capac...High-entropy magnetocaloric alloys offer exceptional compositional flexibility and stability for magnetic refrigeration.However,enhancing their magnetic entropy change,working temperature range,and refrigeration capacity remains challenging.In this study,we demonstrate that microalloying GdTbDyHo with only 0.4at%nonmagnetic Y effectively addresses this limitation.Our analysis indicates that Y uniformly dissolves into the hexagonal matrix lattice,disrupting the 4f–4f exchange interactions and inducing a local short-range order.This weakens the antiferromagnetic coupling,accelerates the antiferromagnetic–ferromagnetic transition,and broadensits range.Consequently,the peak magnetic entropy change increases from 8.2 to 8.7 J·kg^(−1)·K^(−1),the working temperature range expands from 77 to 89 K,and the refrigeration capacity improves by 23%,reaching 774 J·kg^(−1)(5 T)relative to the Y-free alloy,while the Néel temperature remains constant(~195 K).This study establishes nonmagnetic microalloying as a cost-effective and scalable strategy for designing high-performance magnetocaloric materials.展开更多
Conformational entropy,one of the central concepts of polymer physics,is the key to revealing physical characteristics of polymers.Despite an increased repertoire of conformational-entropy effects in the structural fo...Conformational entropy,one of the central concepts of polymer physics,is the key to revealing physical characteristics of polymers.Despite an increased repertoire of conformational-entropy effects in the structural formation,transition,and properties of polymer systems,the physical origin of conformational entropy remains less understood compared to interaction energy and other types of entropy.This review seeks to provide a conceptual framework unveiling several principles and rules of conformational entropy in governing the structures and properties of polymers,from the perspective of fundamental physics and statistical mechanics.First,we focus on the fundamentals of entropy in thermodynamics,leading to the theoretical basis for the elucidation of conformational entropy.Second,we delineate the physical nature of statistics and dissipation of conformational entropy and its essential dependence on the environmental heat bath.Next,we explore the principles of conformational entropy in driving the ordering transitions of various systems of polymers and their nanocomposites,elucidating the emergent and collective behaviors as well as the interplay between energetic interactions and entropy.Moreover,we demonstrate how the concept of conformational entropy is generalized to the biological systems and other soft matters.Finally,we discuss future directions to signify this framework originated from polymers.展开更多
This study explored the impact of sintering time and temperature on the synthesis and formation of high-entropy rare earth oxides(HEOs).By systematically varying the sintering conditions,a series of Lu_(2)Yb_(2)Tm_(2)...This study explored the impact of sintering time and temperature on the synthesis and formation of high-entropy rare earth oxides(HEOs).By systematically varying the sintering conditions,a series of Lu_(2)Yb_(2)Tm_(2)Er_(2)O_(12) samples was synthesized and their structural and chemical properties were analyzed using scanning electron microscopy(SEM)with energy-dispersive X-ray spectroscopy(EDS)elemental mapping,X-ray diffraction(XRD),high-resolution transmission electron microscopy(HRTEM),and X-ray photoelectron spectroscopy(XPS).According to XRD patterns,a single-phase cubic C-type structure is easier to form at higher sintering temperatures(1400-1500℃),with sharper peaks signifying better crystallinity.With longer sintering times improving grain development and homogeneity,SEM research reveals a change in morphology from spherical grains at lower temperatures(1100-1200℃)to blocky grains at higher temperatures(1300-1500℃).HRTEM pictures verified the nanoparticles'strong crystallinity,and at higher temperatures,the lattice fringes widen and become more distinct,indicating better atomic ordering and diffusion.Stable and uniform high-entropy oxide production is indicated by the XPS spectra,which shows uniform elemental distribution and consistent chemical states of the constituent elements with very slight variations in the oxygen peaks.The findings highlight how important the sintering temperature is for reaching the intended high-entropy phase,with higher temperatures promoting improved atomic diffusion and compositional homogeneity.The results open the door for the use of high-entropy rare earth oxides in sophisticated functional materials by offering insightful information on how to best synthesize them.展开更多
High-entropy oxides(HEOs)derive their exceptional properties from the atomic-level homogenization of multiple constituent elements within the crystal lattice,which induces a sophisticated local environment that fundam...High-entropy oxides(HEOs)derive their exceptional properties from the atomic-level homogenization of multiple constituent elements within the crystal lattice,which induces a sophisticated local environment that fundamentally reconfigures electron density distributions and coordination environment at active sites.However,the mechanisms by which multi-component systems in HEOs precisely regulate high-activity catalytic sites remain poorly understood.This work addresses this gap by designing medium-entropy perovskite oxides through the strategic incorporation of transition metals with distinct electronegativities and ionic radii,aiming to unravel how local environmental modifications impact the energy band location,coordination states,and adsorption behavior of the Co site.A family of A_(2)BO_(4)-type medium-entropy oxides PrSr(Fe_(0.2)Co_(0.2)Ni_(0.2)Cu_(0.2)M_(0.2))O_(4)(M=Sc,Cr,Mn)was successfully synthesized.Divergent atomic properties among Sc,Cr,and Mn(electronegativity,ionic size,and metal-oxygen bond strength)triggered pronounced electron redistribution,effectively tuning the d-band center of Co.Remarkably,Cr substitution significantly enhanced O_(2) adsorption at Co-active sites,as indicated by an elongated O-O bond length(1.234Å→1.279Å).Concurrently,Cr doping destabilized the M'-O-Cr bonds(M'=Fe,Co,Ni,Cu)and lowered the thermodynamic barrier for oxygen vacancy formation.Electrochemical tests revealed that PrSr(Fe_(0.2)Co_(0.2)Ni_(0.2)Cu_(0.2)Cr_(0.2))O_(4)(PSMO-Cr)exhibited the highest electrical conductivity and fastest oxygen surface exchange kinetics.At 700℃,the area-specific resistance(ASR)of the PSMO-Cr cathode was 0.07Ωcm^(2).Corresponding fuel cells achieved a maximum power density of 0.76 W cm^(-2).In electrolysis mode,the maximum current density reached 0.56 A cm^(-2) under 1.3 V at 700℃using PSMO-Cr as the anode.These results demonstrate that PSMO-Cr is a promising bifunctional catalyst for energy conversion applications.展开更多
Sintering and coking are critical barriers to achieving high performance in dry reforming of methane(DRM)catalysts.A finely dispersed and thermostable Ni-based catalyst is the key to address these issues.By leveraging...Sintering and coking are critical barriers to achieving high performance in dry reforming of methane(DRM)catalysts.A finely dispersed and thermostable Ni-based catalyst is the key to address these issues.By leveraging the intrinsic superiorities of high-entropy oxides in high-temperature stability and low atomic diffusivity,in this study,a highly dispersed Ni-based catalyst is synthesized via an entropycontrolled exsolution of active components.By increasing the number of transition-metal elements in spinel oxides,the active metalsupport interaction(MSI)can be continuously strengthened,which controls the exsolution and thermal stability of Ni-based active metal in harsh reaction conditions of DRM.An optimized medium-entropy spinel(Mg_(0.4)Ni_(0.2)Co_(0.2)Zn_(0.2))Al_(2)O_(4)with the exsolution of finely dispersed Ni–Co nanoparticles displayed superior activity and stability in thermal DRM at 800°C and photothermal DRM.This entropy-controlled MSI and exsolution principle provides a significant strategy for designing robust catalysts resistant to sintering and coking for high-temperature reactions like DRM in thermal and photothermal systems.展开更多
High entropy alloys(HEAs)have recently attracted significant attention due to their exceptional mechanical properties and potential applications across various fields.Friction stir welding and processing(FSW/P),as not...High entropy alloys(HEAs)have recently attracted significant attention due to their exceptional mechanical properties and potential applications across various fields.Friction stir welding and processing(FSW/P),as notable solid-state welding and processing techniques,have been proved effectiveness in enhancing microstructures and mechanical properties of HEAs.This review article summarizes the current status of FSW/P of HEAs.The welding materials and conditions used for FSW/P in HEAs are reviewed and discussed.The effects of FSW/P on the evolutions of grain structure,texture,dislocation,and secondary phase for different HEAs are highlighted.Furthermore,the influences of FSW/P on the mechanical properties of various HEAs are analyzed.Finally,potential applications,challenges,and future directions of FSW/P in HEAs are forecasted.Overall,FSW/P enable to refine grains of HEAs through dynamic recrystallization and to activate diverse deformation mechanisms of HEAs through tailoring phase structures,thereby significantly improving the strength,hardness,and ductility of both single-and dual-phase HEAs.Future progress in this field will rely on comprehensive optimization of processing parameters and alloy composition,integration of multi-scale modeling with advanced characterization for in-depth exploration of microstructural mechanisms,systematic evaluation of functional properties,and effective bridging of the gap between laboratory research and industrial application.The review aims to provide an overview of recent advancements in the FSW/P of HEAs and encourage further research in this area.展开更多
Selective laser melting(SLM),as an additive manufacturing technology,has garnered widespread attention for its capability to fabricate components with complex geometries and to tailor the microstructure and mechanical...Selective laser melting(SLM),as an additive manufacturing technology,has garnered widespread attention for its capability to fabricate components with complex geometries and to tailor the microstructure and mechanical properties under specific conditions.However,the intrinsic influence mechanism of microstructure formation under non-equilibrium solidification conditions in SLM processes has not been clearly revealed.In the present work,the influence of Al concentration and process parameters on the microstructure forming mechanism of Al_(x)CoCrFeNi HEAs prepared by SLM is investigated by molecular dynamics simulation method.The simulation results show that the difference in Al content significantly affects the microstructure formation of HEAs,including the growth rate and morphology of columnar crystals,stress distribution at grain boundaries,and defect structure.In addition,the results show that increasing the substrate temperature improves the solidification formability,reduces microstructural defects,and helps reduce residual stress in Al_(x)CoCrFeNi HEAs.By analyzing the influence of heat and solute flow in the molten pool on the growth of columnar crystals,it is found that spatial fluctuations in Al concentration during the non-equilibrium solidification process inhibit the high cooling rates induced by steep temperature gradients.These findings promote the understanding of the forming mechanism of microstructure in HEAs prepared by SLM and provide theoretical guidance for designing high-performance SLM-fabricated HEAs.展开更多
A fine-grained metastable dual-phase Fe_(40)Mn_(20)Co_(20)Cr_(15)Si_(5)high entropy alloy(CS-HEA)with excellent strength and ductility was successfully prepared by friction stir processing(FSP).The microstructural and...A fine-grained metastable dual-phase Fe_(40)Mn_(20)Co_(20)Cr_(15)Si_(5)high entropy alloy(CS-HEA)with excellent strength and ductility was successfully prepared by friction stir processing(FSP).The microstructural and mechanical properties of the fine-grained CS-HEA were characterized.The results showed that as-cast shrinkage cavities and elemental segregation were eliminated.The average grain size was refined from 121.1 to 5.4μm.The face-centered cubic phase fraction increased from 23%to 82%.During tensile deformation,dislocation slip dominated at strains ranging from 5%to 17%,followed by transformation induced plasticity(TRIP)from 17%to 26%,and twin induced plasticity(TWIP)from 26%to 37%.The yield strength,ultimate tensile strength,and elongation of the fine-grained CS-HEA were 503 MPa,1120 MPa,and 37%,respectively.The strength-ductility synergy of fine-grained CS-HEA was attributed to the combined effects of TRIP,TWIP,dislocation strengthening,and fine-grained strengthening.展开更多
Rising global temperatures alongside increasing energy demand highlight the imperative for sustainable and energy-efficient refrigeration technologies.Magnetic refrigeration,based on the magnetocaloric effect(MCE),pre...Rising global temperatures alongside increasing energy demand highlight the imperative for sustainable and energy-efficient refrigeration technologies.Magnetic refrigeration,based on the magnetocaloric effect(MCE),presents a compelling solid-state alternative to traditional vapor-compression systems.However,many high-performance magnetocaloric materials rely on critical elements such as rare earths,cobalt and germanium.Despite extensive compositional flexibility,high-entropy alloys(HEAs)have predominantly been investigated in equiatomic compositions incorporating significant quantities of highly critical elements to achieve large MCE or mixing rare-earth elements in majority proportions that only yield moderate MCE values,thereby failing to address issues of material criticality.In this study,we present a criticality-aware design strategy for the MnNiSi-HEA system,exemplifying a prototype of the latest third-generation HEAs.Various substitutional approaches were evaluated to achieve the coupling between magnetic and structural transitions.The most effective pathway,identified through the co-substitution of Fe and Cu reduces the structural transition temperature by over 900 K relative to MnNiSi while preserving the ferromagnetic characteristics of the low-temperature phase,successfully inducing a first-order magnetostructural transformation near room temperature.The resulting alloys,Mn_(0.5)Fe_(0.5)Ni_(1−x)Cu_(x)Si,exhibit coupled transitions spanning more than 100 K and demonstrate the highest MCE reported to date among HEAs free of cobalt,germanium and rare-earth elements,outperforming previous records by 360%.Complementary density functional theory calculations confirm the stability of the orthorhombic and hexagonal phases.Predictions of lattice entropy change closely match calorimetric measurements.This study establishes a new benchmark for low-criticality magnetocaloric HEAs,underscoring that optimal functional performance and sustainable material development can be achieved concomitantly.The proposed design methodology offers a valuable framework for advancing resource-resilient solid-state cooling materials and underscores the potential of HEAs as a platform for sustainable functional materials.展开更多
High‐entropy amorphous catalysts(HEACs)integrate multielement synergy with structural disorder,making them promising candidates for water splitting.Their distinctive features—including flexible coordination environm...High‐entropy amorphous catalysts(HEACs)integrate multielement synergy with structural disorder,making them promising candidates for water splitting.Their distinctive features—including flexible coordination environments,tunable electronic structures,abundant unsaturated active sites,and dynamic structural reassembly—collectively enhance electrochemical activity and durability under operating conditions.This review summarizes recent advances in HEACs for hydrogen evolution,oxygen evolution,and overall water splitting,highlighting their disorder-driven advantages over crystalline counterparts.Catalytic performance benchmarks are presented,and mechanistic insights are discussed,focusing on how multimetallic synergy,amorphization effect,and in‐situ reconstruction cooperatively regulate reaction pathways.These insights provide guidance for the rational design of next‐generation amorphous high‐entropy electrocatalysts with improved efficiency and durability.展开更多
Seismic resilience(SR)has emerged as a critical focus in earthquake engineering to evaluate the ability of structures to endure,recover from,and adapt to seismic events.This study presents an entropy-based multicriter...Seismic resilience(SR)has emerged as a critical focus in earthquake engineering to evaluate the ability of structures to endure,recover from,and adapt to seismic events.This study presents an entropy-based multicriteria approach for selecting optimal intensity measures(IMs)to assess SR of structures.Eight representative IMs,derived from time histories and response spectrum are evaluated.Incremental dynamic analysis is con-ducted on a reinforced concrete structure,using engineering demand parameters such as the maximum interstory drift and floor acceleration to generate fragility curves via a probabilistic seismic demand model.The optimal IMs are identified through a multi-criteria decision-making process,with scores calculated using the entropy weight method to incorporate factors such as efficiency,proficiency,and uncertainty based on infor-mation entropy.An effective SR framework is derived from fragility results.The findings indicate that peak ground velocity and spectral IMs are the most effective,while energy-related IMs underestimate SR.The study highlights the importance of optimizing IMs for more accurate seismic resilience assessments.The proposed entropy-based multi-criteria approach is shown to be both reliable and effective for selecting optimal IMs in this context.展开更多
Conversion of ammonia into hydrogen,a crucial pathway for the hydrogen economy,is severely constrained by the intricacy of the required equipment and the low efficiency.Herein,Pd@Pt Ni Co Ru Ir coreshell mesoporous bi...Conversion of ammonia into hydrogen,a crucial pathway for the hydrogen economy,is severely constrained by the intricacy of the required equipment and the low efficiency.Herein,Pd@Pt Ni Co Ru Ir coreshell mesoporous bifunctional electrocatalysts were fabricated via a one-step wet-chemical reduction approach.By utilizing the limiting effect of triblock copolymers,gradient distribution control of six metal elements(Pd core and Pt/Ni/Co/Ru/Ir high-entropy alloys shell) was achieved,where the high-entropy alloy shell forms high-density active sites through lattice distortion effect.With the help of lattice distortion and mesoporous-confinement-enabled interfacial coupling effects,Pd@Pt Ni Co Ru Ir catalyst exhibited exceptional bifunctional performance in alkaline media:A low hydrogen evolution reaction(HER) overpotential of 30.5 m V at 10 m A/cm^(2) and a high ammonia oxidation reaction(AOR) peak current density of 19.6 m A/cm^(2) at 0.7 V vs.RHE,representing a 3.83-fold enhancement over commercial Pt/C.Moreover,a rechargeable Zn-NH_(3) battery system was constructed and achieved 92.3 % Faradaic efficiency(FE) for NH_(3)-to-H_(2) conversion with outstanding stability at 16 m A/cm^(2),thereby providing an innovative solution for efficient ammonia decomposition-based hydrogen production.展开更多
Valence state engineering has emerged as a powerful strategy to optimize catalytic performance by modulating the electronic structure of metal active sites.However,the valence state regulation in high-entropy compound...Valence state engineering has emerged as a powerful strategy to optimize catalytic performance by modulating the electronic structure of metal active sites.However,the valence state regulation in high-entropy compounds(HECs)remains elusive due to their complex multi-element components and electronic interactions.Here,the valence states of different metals in twodimensional(2D)high entropy oxide(HEO)(FeNiMoRuV)O_(2-x)are precisely modulated through controlled pyrolysis of corresponding 2D high entropy hydroxide(HEHO)(FeNiMoRuV)(OH)_(2)under varying temperatures.Temperature-controlled pyrolysis selectively reduces the oxidation state of Ru,while simultaneously increasing the valence state of other constituent metals(Fe,Ni,Mo,and V),suggesting a competitive redox equilibrium.Notably,these low-valence Ru sites with oxygen vacancy in 2D HEO significantly reduce Ru-O bond energy and promote the generation of O-^(O)intermediates,thereby enabling oxygen evolution with a lattice oxygen mediated-oxygen vacancy site mechanism.2D HEO with low-valence Ru exhibits superior electrolytic water performance(HER/OER)compared to HEHO and other HEO with high-valence Ru,achieving a current density of 1000 mA cm^(-2)at 1.923 V,which exceeds the commercial Pt/C‖RuO_(2)system.Therefore,this study reveals the valence state regulatory mechanism of HECs and provides a solid hammer for the catalytic mechanism of valence state engineering.展开更多
In recent years,medium entropy alloys have become a research hotspot due to their excellent physical and chemical performances.By controlling reasonable elemental composition and processing parameters,the medium entro...In recent years,medium entropy alloys have become a research hotspot due to their excellent physical and chemical performances.By controlling reasonable elemental composition and processing parameters,the medium entropy alloys can exhibit similar properties to high entropy alloys and have lower costs.In this paper,a FeCoNi medium entropy alloy precursor was prepared via sol-gel and coprecipitation methods,respectively,and FeCoNi medium entropy alloys were prepared by carbothermal and hydrogen reduction.The phases and magnetic properties of FeCoNi medium entropy alloy were investigated.Results showed that FeCoNi medium entropy alloy was produced by carbothermal and hydrogen reduction at 1500℃.Some carbon was detected in the FeCoNi medium entropy alloy prepared by carbothermal reduction.The alloy prepared by hydrogen reduction was uniform and showed a relatively high purity.Moreover,the hydrogen reduction product exhibited better saturation magnetization and lower coercivity.展开更多
This study investigated the physicochemical properties,enzyme activities,volatile flavor components,microbial communities,and sensory evaluation of high-temperature Daqu(HTD)during the maturation process,and a standar...This study investigated the physicochemical properties,enzyme activities,volatile flavor components,microbial communities,and sensory evaluation of high-temperature Daqu(HTD)during the maturation process,and a standard system was established for comprehensive quality evaluation of HTD.There were obvious changes in the physicochemical properties,enzyme activities,and volatile flavor components at different storage periods,which affected the sensory evaluation of HTD to a certain extent.The results of high-throughput sequencing revealed significant microbial diversity,and showed that the bacterial community changed significantly more than did the fungal community.During the storage process,the dominant bacterial genera were Kroppenstedtia and Thermoascus.The correlation between dominant microorganisms and quality indicators highlighted their role in HTD quality.Lactococcus,Candida,Pichia,Paecilomyces,and protease activity played a crucial role in the formation of isovaleraldehyde.Acidic protease activity had the greatest impact on the microbial community.Moisture promoted isobutyric acid generation.Furthermore,the comprehensive quality evaluation standard system was established by the entropy weight method combined with multi-factor fuzzy mathematics.Consequently,this study provides innovative insights for comprehensive quality evaluation of HTD during storage and establishes a groundwork for scientific and rational storage of HTD and quality control of sauce-flavor Baijiu.展开更多
基金supported by the Fujian Provincial Science and Technology Planning Project(No.2022HZ027006,No.2024HZ021023)National Natural Science Foundation of China(No.U22A20118).
文摘High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical strength,and outstanding catalytic activity.These distinctive characteristics render HEMs highly suitable for various battery components,such as electrodes,electrolytes,and catalysts.This review systematically examines recent advances in the application of HEMs for energy storage,beginning with fundamental concepts,historical development,and key definitions.Three principal categories of HEMs,namely high-entropy alloys,high-entropy oxides,and highentropy MXenes,are analyzed with a focus on electrochemical performance metrics such as specific capacity,energy density,cycling stability,and rate capability.The underlying mechanisms by which these materials enhance battery performance are elucidated in the discussion.Furthermore,the pivotal role of machine learning in accelerating the discovery and optimization of novel high-entropy battery materials is highlighted.The review concludes by outlining future research directions and potential breakthroughs in HEM-based battery technologies.
基金funded by the Ministry of Higher Education,Malaysia,under the Fundamental Research Grant Scheme FRGS/1/2023/STG06/UM/02/4(Project FP069-2023)。
文摘Electroosmotic transport and entropy generation play a decisive role in regulating efficiency,stability,and energy cost of non-Newtonian nanoblood flows in stenosed arteries,particularly with tapered geometries.Thisstudy develops a unified model to analyze ZnO-Williamson nanoblood flow through a stenosed artery with converging,diverging,and non-tapered configurations,incorporating electroosmosis,viscous dissipation,and entropy production.The arterial walls are assumed to be electrically charged with a no-slip condition to induce electroosmotic propulsionalong the endothelial surface.The partial differential equations are nondimensionalized to a coupled system ofnonlinear ordinary differential equations,which are solved numerically using a MATLAB-based shooting technique.Parametric investigation is conducted for Brinkman,Grashof,and Weissenberg numbers,ZnO fractional volume,volumetric flow rate,and Helmholtz-Smoluchowski velocity to quantify their influences on axial velocity,wall shearstress,impedance resistance,temperature distribution,entropy generation,Bejan number,and streamline topology.The axial velocity decreases radially with increasing Brinkman number for all arterial geometries.Increasing ZnOnanoparticles improves thermal transport owing to enhanced effective thermal conductivity but simultaneously elevatesentropy generation due to increased viscous dissipation.Higher Weissenberg numbers suppress entropy production bypromoting elastic stress redistribution and lowering shear-induced irreversibility.Impedance resistance decreases withincreasing stenosis height but increases with stenosis shape parameter and ZnO fractional volume.Streamline analysisshows that buoyancy and viscoelasticity significantly distort flow near the stenosis,while increasing electroosmoticvelocity stabilizes streamlines,suppresses recirculation,and reduces local shear stress and pressure fluctuations.Inconclusion,electroosmotic actuation is most effective in reducing flow resistance in the converging tapered artery,particularly at lower ZnO volume fractions.Overall,the findings highlight the potential of optimized electroosmoticactuation and controlled nanoparticle loading to minimize thermodynamic losses,regulate shear stress,and improveflow uniformity in stenosed vessels,with promising implications for electro-assisted drug delivery,nanotherapeutics,and bio-inspired vascular microfluidic systems.
基金financially supported by the National Natural Science Foundation of China(Grant No.12172093)the Guangdong Basic and Applied Basic Research Foundation(Grant No.2021A1515012607)。
文摘High-entropy oxides(HEOs)have emerged as a promising class of memristive materials,characterized by entropy-stabilized crystal structures,multivalent cation coordination,and tunable defect landscapes.These intrinsic features enable forming-free resistive switching,multilevel conductance modulation,and synaptic plasticity,making HEOs attractive for neuromorphic computing.This review outlines recent progress in HEO-based memristors across materials engineering,switching mechanisms,and synaptic emulation.Particular attention is given to vacancy migration,phase transitions,and valence-state dynamics—mechanisms that underlie the switching behaviors observed in both amorphous and crystalline systems.Their relevance to neuromorphic functions such as short-term plasticity and spike-timing-dependent learning is also examined.While encouraging results have been achieved at the device level,challenges remain in conductance precision,variability control,and scalable integration.Addressing these demands a concerted effort across materials design,interface optimization,and task-aware modeling.With such integration,HEO memristors offer a compelling pathway toward energy-efficient and adaptable brain-inspired electronics.
基金supported by the National Natural Science Foundation of China(Nos.92166105 and 52005053)High-Tech Industry Science and Technology Innovation Leading Program of Hunan Province(No.2020GK2085)the Science and Technology Innovation Program of Hunan Province(No.2021RC3096).
文摘(NbZrHfTi)C high-entropy ceramics,as an emerging class of ultra-high-temperature materials,have garnered significant interest due to their unique multi-principal-element crystal structure and exceptional hightemperature properties.This study systematically investigates the mechanical properties of(NbZrHfTi)C high-entropy ceramics by employing first-principles density functional theory,combined with the Debye-Grüneisen model,to explore the variations in their thermophysical properties with temperature(0–2000 K)and pressure(0–30 GPa).Thermodynamically,the calculated mixing enthalpy and Gibbs free energy confirm the feasibility of forming a stable single-phase solid solution in(NbZrHfTi)C.The calculated results of the elastic stiffness constant indicate that the material meets the mechanical stability criteria of the cubic crystal system,further confirming the structural stability.Through evaluation of key mechanical parameters—bulk modulus,shear modulus,Young’s modulus,and Poisson’s ratio—we provide comprehensive insight into the macro-mechanical behaviour of the material and its correlation with the underlying microstructure.Notably,compared to traditional binary carbides and their average properties,(NbZrHfTi)C exhibits higher Vickers hardness(Approximately 28.5 GPa)and fracture toughness(Approximately 3.4 MPa⋅m^(1/2)),which can be primarily attributed to the lattice distortion and solid-solution strengthening mechanism.The study also utilizes the quasi-harmonic approximation method to predict the material’s thermophysical properties,including Debye temperature(initial value around 563 K),thermal expansion coefficient(approximately 8.9×10^(−6) K−1 at 2000 K),and other key parameters such as heat capacity at constant volume.The results show that within the studied pressure and temperature ranges,(NbZrHfTi)C consistently maintains a stable phase structure and good thermomechanical properties.The thermal expansion coefficient increasing with temperature,while heat capacity approaches the Dulong-Petit limit at elevated temperatures.These findings underscore the potential of(NbZrHfTi)C applications in ultra-high temperature thermal protection systems,cutting tool coatings,and nuclear structural materials.
基金financially supported by the National Sci-ence Foundation for Young Scientists of China(Nos.52201172,52201171,52401219)the National Science Fund for Distinguished Young Scholars(No.52225103)+4 种基金the National Natural Science Foundation of China(No.52130108)the National Key R&D Program of China(No.2022YFB4602101)the Joint Funds of the National Natural Science Foundation of China(No.U2441262)the Funds for International Cooperation and Exchange of the National Nat-ural Science Foundation of China(No.W2412068)the Fundamental Research Fund for the Central Universities of China(No.FRF-TP-22-001C2).
文摘High-entropy magnetocaloric alloys offer exceptional compositional flexibility and stability for magnetic refrigeration.However,enhancing their magnetic entropy change,working temperature range,and refrigeration capacity remains challenging.In this study,we demonstrate that microalloying GdTbDyHo with only 0.4at%nonmagnetic Y effectively addresses this limitation.Our analysis indicates that Y uniformly dissolves into the hexagonal matrix lattice,disrupting the 4f–4f exchange interactions and inducing a local short-range order.This weakens the antiferromagnetic coupling,accelerates the antiferromagnetic–ferromagnetic transition,and broadensits range.Consequently,the peak magnetic entropy change increases from 8.2 to 8.7 J·kg^(−1)·K^(−1),the working temperature range expands from 77 to 89 K,and the refrigeration capacity improves by 23%,reaching 774 J·kg^(−1)(5 T)relative to the Y-free alloy,while the Néel temperature remains constant(~195 K).This study establishes nonmagnetic microalloying as a cost-effective and scalable strategy for designing high-performance magnetocaloric materials.
基金financially supported by the National Natural Science Foundation of China (Nos. 22533003 and 22025302)financial support from the Ministry of Science and Technology of China (No. 2022YFA1203203)State Key Laboratory of Chemical Engineering (No. SKL-ChE23T01).
文摘Conformational entropy,one of the central concepts of polymer physics,is the key to revealing physical characteristics of polymers.Despite an increased repertoire of conformational-entropy effects in the structural formation,transition,and properties of polymer systems,the physical origin of conformational entropy remains less understood compared to interaction energy and other types of entropy.This review seeks to provide a conceptual framework unveiling several principles and rules of conformational entropy in governing the structures and properties of polymers,from the perspective of fundamental physics and statistical mechanics.First,we focus on the fundamentals of entropy in thermodynamics,leading to the theoretical basis for the elucidation of conformational entropy.Second,we delineate the physical nature of statistics and dissipation of conformational entropy and its essential dependence on the environmental heat bath.Next,we explore the principles of conformational entropy in driving the ordering transitions of various systems of polymers and their nanocomposites,elucidating the emergent and collective behaviors as well as the interplay between energetic interactions and entropy.Moreover,we demonstrate how the concept of conformational entropy is generalized to the biological systems and other soft matters.Finally,we discuss future directions to signify this framework originated from polymers.
基金Project supported by Natural Science Foundation of Zhejiang Province(LD21E080001)Zhejiang Provincial Ten Thousand Talent Program(ZJWR0302055)。
文摘This study explored the impact of sintering time and temperature on the synthesis and formation of high-entropy rare earth oxides(HEOs).By systematically varying the sintering conditions,a series of Lu_(2)Yb_(2)Tm_(2)Er_(2)O_(12) samples was synthesized and their structural and chemical properties were analyzed using scanning electron microscopy(SEM)with energy-dispersive X-ray spectroscopy(EDS)elemental mapping,X-ray diffraction(XRD),high-resolution transmission electron microscopy(HRTEM),and X-ray photoelectron spectroscopy(XPS).According to XRD patterns,a single-phase cubic C-type structure is easier to form at higher sintering temperatures(1400-1500℃),with sharper peaks signifying better crystallinity.With longer sintering times improving grain development and homogeneity,SEM research reveals a change in morphology from spherical grains at lower temperatures(1100-1200℃)to blocky grains at higher temperatures(1300-1500℃).HRTEM pictures verified the nanoparticles'strong crystallinity,and at higher temperatures,the lattice fringes widen and become more distinct,indicating better atomic ordering and diffusion.Stable and uniform high-entropy oxide production is indicated by the XPS spectra,which shows uniform elemental distribution and consistent chemical states of the constituent elements with very slight variations in the oxygen peaks.The findings highlight how important the sintering temperature is for reaching the intended high-entropy phase,with higher temperatures promoting improved atomic diffusion and compositional homogeneity.The results open the door for the use of high-entropy rare earth oxides in sophisticated functional materials by offering insightful information on how to best synthesize them.
基金supported by the National Natural Science Foundation of China(51872078,52272197,52572219)Heilongjiang Provincial Natural Science Foundation of China(LH2024E106)。
文摘High-entropy oxides(HEOs)derive their exceptional properties from the atomic-level homogenization of multiple constituent elements within the crystal lattice,which induces a sophisticated local environment that fundamentally reconfigures electron density distributions and coordination environment at active sites.However,the mechanisms by which multi-component systems in HEOs precisely regulate high-activity catalytic sites remain poorly understood.This work addresses this gap by designing medium-entropy perovskite oxides through the strategic incorporation of transition metals with distinct electronegativities and ionic radii,aiming to unravel how local environmental modifications impact the energy band location,coordination states,and adsorption behavior of the Co site.A family of A_(2)BO_(4)-type medium-entropy oxides PrSr(Fe_(0.2)Co_(0.2)Ni_(0.2)Cu_(0.2)M_(0.2))O_(4)(M=Sc,Cr,Mn)was successfully synthesized.Divergent atomic properties among Sc,Cr,and Mn(electronegativity,ionic size,and metal-oxygen bond strength)triggered pronounced electron redistribution,effectively tuning the d-band center of Co.Remarkably,Cr substitution significantly enhanced O_(2) adsorption at Co-active sites,as indicated by an elongated O-O bond length(1.234Å→1.279Å).Concurrently,Cr doping destabilized the M'-O-Cr bonds(M'=Fe,Co,Ni,Cu)and lowered the thermodynamic barrier for oxygen vacancy formation.Electrochemical tests revealed that PrSr(Fe_(0.2)Co_(0.2)Ni_(0.2)Cu_(0.2)Cr_(0.2))O_(4)(PSMO-Cr)exhibited the highest electrical conductivity and fastest oxygen surface exchange kinetics.At 700℃,the area-specific resistance(ASR)of the PSMO-Cr cathode was 0.07Ωcm^(2).Corresponding fuel cells achieved a maximum power density of 0.76 W cm^(-2).In electrolysis mode,the maximum current density reached 0.56 A cm^(-2) under 1.3 V at 700℃using PSMO-Cr as the anode.These results demonstrate that PSMO-Cr is a promising bifunctional catalyst for energy conversion applications.
基金supported by the National Key R&D Program of China(2023YFB4104600)National Natural Science Foundation of China(52572313)+1 种基金Tangshan Talent Funding Project(A202202007)Shenzhen Science and Technology Innovation Commission under Grant No.20231120185819001。
文摘Sintering and coking are critical barriers to achieving high performance in dry reforming of methane(DRM)catalysts.A finely dispersed and thermostable Ni-based catalyst is the key to address these issues.By leveraging the intrinsic superiorities of high-entropy oxides in high-temperature stability and low atomic diffusivity,in this study,a highly dispersed Ni-based catalyst is synthesized via an entropycontrolled exsolution of active components.By increasing the number of transition-metal elements in spinel oxides,the active metalsupport interaction(MSI)can be continuously strengthened,which controls the exsolution and thermal stability of Ni-based active metal in harsh reaction conditions of DRM.An optimized medium-entropy spinel(Mg_(0.4)Ni_(0.2)Co_(0.2)Zn_(0.2))Al_(2)O_(4)with the exsolution of finely dispersed Ni–Co nanoparticles displayed superior activity and stability in thermal DRM at 800°C and photothermal DRM.This entropy-controlled MSI and exsolution principle provides a significant strategy for designing robust catalysts resistant to sintering and coking for high-temperature reactions like DRM in thermal and photothermal systems.
基金supported by National Natural Science Foundation of China(Grant No.52171032)Hebei Natural Science Foundation(Grant No.E2023501002)Fundamental Research Funds for the Central Universities(Grant No.2024GFYD003)。
文摘High entropy alloys(HEAs)have recently attracted significant attention due to their exceptional mechanical properties and potential applications across various fields.Friction stir welding and processing(FSW/P),as notable solid-state welding and processing techniques,have been proved effectiveness in enhancing microstructures and mechanical properties of HEAs.This review article summarizes the current status of FSW/P of HEAs.The welding materials and conditions used for FSW/P in HEAs are reviewed and discussed.The effects of FSW/P on the evolutions of grain structure,texture,dislocation,and secondary phase for different HEAs are highlighted.Furthermore,the influences of FSW/P on the mechanical properties of various HEAs are analyzed.Finally,potential applications,challenges,and future directions of FSW/P in HEAs are forecasted.Overall,FSW/P enable to refine grains of HEAs through dynamic recrystallization and to activate diverse deformation mechanisms of HEAs through tailoring phase structures,thereby significantly improving the strength,hardness,and ductility of both single-and dual-phase HEAs.Future progress in this field will rely on comprehensive optimization of processing parameters and alloy composition,integration of multi-scale modeling with advanced characterization for in-depth exploration of microstructural mechanisms,systematic evaluation of functional properties,and effective bridging of the gap between laboratory research and industrial application.The review aims to provide an overview of recent advancements in the FSW/P of HEAs and encourage further research in this area.
基金supported by the National Natural Science Foundation of China(Grant No.12102133).
文摘Selective laser melting(SLM),as an additive manufacturing technology,has garnered widespread attention for its capability to fabricate components with complex geometries and to tailor the microstructure and mechanical properties under specific conditions.However,the intrinsic influence mechanism of microstructure formation under non-equilibrium solidification conditions in SLM processes has not been clearly revealed.In the present work,the influence of Al concentration and process parameters on the microstructure forming mechanism of Al_(x)CoCrFeNi HEAs prepared by SLM is investigated by molecular dynamics simulation method.The simulation results show that the difference in Al content significantly affects the microstructure formation of HEAs,including the growth rate and morphology of columnar crystals,stress distribution at grain boundaries,and defect structure.In addition,the results show that increasing the substrate temperature improves the solidification formability,reduces microstructural defects,and helps reduce residual stress in Al_(x)CoCrFeNi HEAs.By analyzing the influence of heat and solute flow in the molten pool on the growth of columnar crystals,it is found that spatial fluctuations in Al concentration during the non-equilibrium solidification process inhibit the high cooling rates induced by steep temperature gradients.These findings promote the understanding of the forming mechanism of microstructure in HEAs prepared by SLM and provide theoretical guidance for designing high-performance SLM-fabricated HEAs.
基金the funds of the National Natural Science Fund for Excellent Young Scholars of China(No.52222410)Shaanxi Province National Science Fund for Distinguished Young Scholars,China(No.2022JC-24)the National Natural Science Foundation of China(Nos.52227807,52034005)。
文摘A fine-grained metastable dual-phase Fe_(40)Mn_(20)Co_(20)Cr_(15)Si_(5)high entropy alloy(CS-HEA)with excellent strength and ductility was successfully prepared by friction stir processing(FSP).The microstructural and mechanical properties of the fine-grained CS-HEA were characterized.The results showed that as-cast shrinkage cavities and elemental segregation were eliminated.The average grain size was refined from 121.1 to 5.4μm.The face-centered cubic phase fraction increased from 23%to 82%.During tensile deformation,dislocation slip dominated at strains ranging from 5%to 17%,followed by transformation induced plasticity(TRIP)from 17%to 26%,and twin induced plasticity(TWIP)from 26%to 37%.The yield strength,ultimate tensile strength,and elongation of the fine-grained CS-HEA were 503 MPa,1120 MPa,and 37%,respectively.The strength-ductility synergy of fine-grained CS-HEA was attributed to the combined effects of TRIP,TWIP,dislocation strengthening,and fine-grained strengthening.
基金funded by the European Union within CoCoMag Project(Grant No.101099736)Project PID2023-146047OB-I00(from AEI/10.13039/501100011033)+3 种基金Project PPIT2024-31833,co-financed by EU,Ministerio de Hacienda y Función Publica,FEDER and Junta de Andalucía,and VII Plan Propio de Investigación from University of SevilleE.G.A.acknowledges an FPU scholarship(Ref.FPU23/03426)from the Spanish MICIUC.R.M.acknowledges financial support by the Ramón y Cajal program of the Spanish Ministry of Science and Innovation(Ref.RYC2021-031176-I)J.Y.L.acknowledges an EMERGIA 2021 fellowship from Junta de Andalucía(Ref.EMC21_00418).
文摘Rising global temperatures alongside increasing energy demand highlight the imperative for sustainable and energy-efficient refrigeration technologies.Magnetic refrigeration,based on the magnetocaloric effect(MCE),presents a compelling solid-state alternative to traditional vapor-compression systems.However,many high-performance magnetocaloric materials rely on critical elements such as rare earths,cobalt and germanium.Despite extensive compositional flexibility,high-entropy alloys(HEAs)have predominantly been investigated in equiatomic compositions incorporating significant quantities of highly critical elements to achieve large MCE or mixing rare-earth elements in majority proportions that only yield moderate MCE values,thereby failing to address issues of material criticality.In this study,we present a criticality-aware design strategy for the MnNiSi-HEA system,exemplifying a prototype of the latest third-generation HEAs.Various substitutional approaches were evaluated to achieve the coupling between magnetic and structural transitions.The most effective pathway,identified through the co-substitution of Fe and Cu reduces the structural transition temperature by over 900 K relative to MnNiSi while preserving the ferromagnetic characteristics of the low-temperature phase,successfully inducing a first-order magnetostructural transformation near room temperature.The resulting alloys,Mn_(0.5)Fe_(0.5)Ni_(1−x)Cu_(x)Si,exhibit coupled transitions spanning more than 100 K and demonstrate the highest MCE reported to date among HEAs free of cobalt,germanium and rare-earth elements,outperforming previous records by 360%.Complementary density functional theory calculations confirm the stability of the orthorhombic and hexagonal phases.Predictions of lattice entropy change closely match calorimetric measurements.This study establishes a new benchmark for low-criticality magnetocaloric HEAs,underscoring that optimal functional performance and sustainable material development can be achieved concomitantly.The proposed design methodology offers a valuable framework for advancing resource-resilient solid-state cooling materials and underscores the potential of HEAs as a platform for sustainable functional materials.
基金supported by the Australian Research Council(ARC)Projects(DP220101139,DP220101142,and LP240100542).
文摘High‐entropy amorphous catalysts(HEACs)integrate multielement synergy with structural disorder,making them promising candidates for water splitting.Their distinctive features—including flexible coordination environments,tunable electronic structures,abundant unsaturated active sites,and dynamic structural reassembly—collectively enhance electrochemical activity and durability under operating conditions.This review summarizes recent advances in HEACs for hydrogen evolution,oxygen evolution,and overall water splitting,highlighting their disorder-driven advantages over crystalline counterparts.Catalytic performance benchmarks are presented,and mechanistic insights are discussed,focusing on how multimetallic synergy,amorphization effect,and in‐situ reconstruction cooperatively regulate reaction pathways.These insights provide guidance for the rational design of next‐generation amorphous high‐entropy electrocatalysts with improved efficiency and durability.
基金partly supported by Engineering Partners Inter-national,LLC,Richfield,MN 55423(PC13803,482842-58309).
文摘Seismic resilience(SR)has emerged as a critical focus in earthquake engineering to evaluate the ability of structures to endure,recover from,and adapt to seismic events.This study presents an entropy-based multicriteria approach for selecting optimal intensity measures(IMs)to assess SR of structures.Eight representative IMs,derived from time histories and response spectrum are evaluated.Incremental dynamic analysis is con-ducted on a reinforced concrete structure,using engineering demand parameters such as the maximum interstory drift and floor acceleration to generate fragility curves via a probabilistic seismic demand model.The optimal IMs are identified through a multi-criteria decision-making process,with scores calculated using the entropy weight method to incorporate factors such as efficiency,proficiency,and uncertainty based on infor-mation entropy.An effective SR framework is derived from fragility results.The findings indicate that peak ground velocity and spectral IMs are the most effective,while energy-related IMs underestimate SR.The study highlights the importance of optimizing IMs for more accurate seismic resilience assessments.The proposed entropy-based multi-criteria approach is shown to be both reliable and effective for selecting optimal IMs in this context.
基金provided by the National Natural Science Foundation of China (No.52573275)Taishan Scholars Program of Shandong Province (No.tsqn202507205)+4 种基金Youth Innovation Team of Higher Education Institutions in Shandong Province (No.2023KJ105)Collaborative Innovation Center of Yellow River Basin Pharmaceutical Green Manufacturing and Engineering Equipment,University of Jinan,Jinan 250022,ChinaJinan City University Integration Development Strategy Project (No.JNSX2023021)supported by Talents’ plan Foundation of Guangdong Second Provincial General Hospital (No.2024D003)Science and Technology Projects in Guangzhou (No.2025A04J4629)。
文摘Conversion of ammonia into hydrogen,a crucial pathway for the hydrogen economy,is severely constrained by the intricacy of the required equipment and the low efficiency.Herein,Pd@Pt Ni Co Ru Ir coreshell mesoporous bifunctional electrocatalysts were fabricated via a one-step wet-chemical reduction approach.By utilizing the limiting effect of triblock copolymers,gradient distribution control of six metal elements(Pd core and Pt/Ni/Co/Ru/Ir high-entropy alloys shell) was achieved,where the high-entropy alloy shell forms high-density active sites through lattice distortion effect.With the help of lattice distortion and mesoporous-confinement-enabled interfacial coupling effects,Pd@Pt Ni Co Ru Ir catalyst exhibited exceptional bifunctional performance in alkaline media:A low hydrogen evolution reaction(HER) overpotential of 30.5 m V at 10 m A/cm^(2) and a high ammonia oxidation reaction(AOR) peak current density of 19.6 m A/cm^(2) at 0.7 V vs.RHE,representing a 3.83-fold enhancement over commercial Pt/C.Moreover,a rechargeable Zn-NH_(3) battery system was constructed and achieved 92.3 % Faradaic efficiency(FE) for NH_(3)-to-H_(2) conversion with outstanding stability at 16 m A/cm^(2),thereby providing an innovative solution for efficient ammonia decomposition-based hydrogen production.
基金supported by the National Natural Science Foundation of China(22205209)China Postdoctoral Science Foundation(2024T170837 and2022M722867)+2 种基金Joint Fund for Provincial Scientific Research and Development Plan of Henan Province(242301420039)the Key Research Projects of Higher Education Institutions of Henan Province(24A530009)Special Fund for Young Teachers from the Zhengzhou University(JC23257011)。
文摘Valence state engineering has emerged as a powerful strategy to optimize catalytic performance by modulating the electronic structure of metal active sites.However,the valence state regulation in high-entropy compounds(HECs)remains elusive due to their complex multi-element components and electronic interactions.Here,the valence states of different metals in twodimensional(2D)high entropy oxide(HEO)(FeNiMoRuV)O_(2-x)are precisely modulated through controlled pyrolysis of corresponding 2D high entropy hydroxide(HEHO)(FeNiMoRuV)(OH)_(2)under varying temperatures.Temperature-controlled pyrolysis selectively reduces the oxidation state of Ru,while simultaneously increasing the valence state of other constituent metals(Fe,Ni,Mo,and V),suggesting a competitive redox equilibrium.Notably,these low-valence Ru sites with oxygen vacancy in 2D HEO significantly reduce Ru-O bond energy and promote the generation of O-^(O)intermediates,thereby enabling oxygen evolution with a lattice oxygen mediated-oxygen vacancy site mechanism.2D HEO with low-valence Ru exhibits superior electrolytic water performance(HER/OER)compared to HEHO and other HEO with high-valence Ru,achieving a current density of 1000 mA cm^(-2)at 1.923 V,which exceeds the commercial Pt/C‖RuO_(2)system.Therefore,this study reveals the valence state regulatory mechanism of HECs and provides a solid hammer for the catalytic mechanism of valence state engineering.
基金financially supported by the National Natural Science Foundation of China(Nos.52074078 and 52374327)the Applied Fundamental Research Program of Liaoning Province,China(No.2023JH2/101600002)+3 种基金the Liaoning Provincial Natural Science Foundation,China(No.2022-YQ-09)the Shenyang Young Middle-Aged Scientific and Technological Innovation Talent Support Program,China(No.RC220491)the Liaoning Province Steel Industry-University-Research Innovation Alliance Cooperation Project of Bensteel Group,China(No.KJBLM202202)the Fundamental Research Funds for the Central Universities,China(Nos.N2201023 and N2325009)。
文摘In recent years,medium entropy alloys have become a research hotspot due to their excellent physical and chemical performances.By controlling reasonable elemental composition and processing parameters,the medium entropy alloys can exhibit similar properties to high entropy alloys and have lower costs.In this paper,a FeCoNi medium entropy alloy precursor was prepared via sol-gel and coprecipitation methods,respectively,and FeCoNi medium entropy alloys were prepared by carbothermal and hydrogen reduction.The phases and magnetic properties of FeCoNi medium entropy alloy were investigated.Results showed that FeCoNi medium entropy alloy was produced by carbothermal and hydrogen reduction at 1500℃.Some carbon was detected in the FeCoNi medium entropy alloy prepared by carbothermal reduction.The alloy prepared by hydrogen reduction was uniform and showed a relatively high purity.Moreover,the hydrogen reduction product exhibited better saturation magnetization and lower coercivity.
文摘This study investigated the physicochemical properties,enzyme activities,volatile flavor components,microbial communities,and sensory evaluation of high-temperature Daqu(HTD)during the maturation process,and a standard system was established for comprehensive quality evaluation of HTD.There were obvious changes in the physicochemical properties,enzyme activities,and volatile flavor components at different storage periods,which affected the sensory evaluation of HTD to a certain extent.The results of high-throughput sequencing revealed significant microbial diversity,and showed that the bacterial community changed significantly more than did the fungal community.During the storage process,the dominant bacterial genera were Kroppenstedtia and Thermoascus.The correlation between dominant microorganisms and quality indicators highlighted their role in HTD quality.Lactococcus,Candida,Pichia,Paecilomyces,and protease activity played a crucial role in the formation of isovaleraldehyde.Acidic protease activity had the greatest impact on the microbial community.Moisture promoted isobutyric acid generation.Furthermore,the comprehensive quality evaluation standard system was established by the entropy weight method combined with multi-factor fuzzy mathematics.Consequently,this study provides innovative insights for comprehensive quality evaluation of HTD during storage and establishes a groundwork for scientific and rational storage of HTD and quality control of sauce-flavor Baijiu.
