Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoa...Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoanodes via an interface-engineered hydrothermal growth followed by rapid thermal annealing(RTA).A TiO_(2)interfacial layer plays a crucial role in ensuring homogeneous precursor deposition,enhancing light absorption,and forming efficient heterojunctions with Sb_(2)S_(3),thereby significantly improving charge separation and transport.RTA further improves crystallinity and interfacial contact,resulting in dense and uniform Sb_(2)S_(3)films with enlarged grains and fewer defects.The optimized Sb_(2)S_(3)photoanode achieves a photocurrent density of 2.51 mA/cm^(2)at 1.23 V vs.the reversible hydrogen electrode(RHE),one of the highest reported for Sb_(2)S_(3)without additional catalysts or passivation layers.To overcome the limitations of oxygen evolution reaction(OER),we employ the iodide oxidation reaction(IOR)as an alternative,significantly lowering the overpotential and improving charge transfer kinetics.Consequently,it produces a record photocurrent density of 8.9 mA/cm^(2)at 0.54 V vs.RHE.This work highlights the synergy between TiO_(2)interfacial engineering,RTA-induced crystallization,and IOR-driven oxidation,offering a promising pathway for efficient and scalable PEC hydrogen production.展开更多
In secondary Al-Si based alloys,microalloying with Mn and Cr can modify harmful platelet-type Alx Fey Siz intermetallic phases to less detrimentalα-Alx(Fe,Mn,Cr)_(y)Siz phase(script or polygonal morphologies).However...In secondary Al-Si based alloys,microalloying with Mn and Cr can modify harmful platelet-type Alx Fey Siz intermetallic phases to less detrimentalα-Alx(Fe,Mn,Cr)_(y)Siz phase(script or polygonal morphologies).However,theα-Alx(Fe,Mn,Cr)_(y)Siz phase morphology,phase composition and the addition of Fecorrecting elements can be influenced by solidification conditions.Therefore,this research is aimed to highlight the morphological evolution and mechanisms ofα-Alx(Fe,Mn,Cr)_(y)Si_(z)phase in a Cr added Al-9%Si-1%Fe-0.2%Cr(all weight percentage thereafter,unless otherwise stated)alloy with varying Mn concentrations(0.25%,0.5%,and 0.8%).Microstructure evolution of Fe intermetallic phases is investi-gated under different casting conditions using a wedge-shaped die,Cu-chill block and melt quenching experiments.Thermodynamic simulations have been performed using CALculation of PHAse Diagrams(CALPHAD)method and compared with the experimental results for phase composition and formation temperatures ofα-Alx(Fe,Mn,Cr)_(y)Siz phase.The results indicated that for 0.25Mn-0.2Cr addition to Al-9Si-1Fe alloy,compact morphology containing polygonal phases are formed in Cu-chill casting,while the wedge castings predominantly show a mixed structure with platelets and script type morphologies.Tensile tests revealed a higher elongation value of 6.6%for mixed structure with platelet and script phases,which is decreased to 4.2%for polygonal phases in Al-9Si-1Fe-0.2Cr-0.25Mn alloy.This study highlights the importance of solidification conditions on morphologies of Fe-intermetallic phases and the mechanical properties by comparing selected literature relevant to high pressure die-casting process.展开更多
In engineering structures, the application of advanced alloys, such as the VCoNi medium-entropy alloy (VCoNi-MEA), with remarkable tensile strength (> 1 GPa) and superior ductility necessitates the employment of di...In engineering structures, the application of advanced alloys, such as the VCoNi medium-entropy alloy (VCoNi-MEA), with remarkable tensile strength (> 1 GPa) and superior ductility necessitates the employment of dissimilar joints. This study pioneers the dissimilar joining of VCoNi-MEA and 17–4 precipitation hardening stainless steel (17–4PH STS) using state-of-the-art green laser beam welding (LBW). To evaluate and optimize the experimental parameters, two welding speeds (200 and 300 mm/s) along with post-weld heat treatment (PWHT) were incorporated. High-quality welded joints with a single-phase face-centered cubic (FCC) structure in the fusion zone (FZ), minimal precipitates (< 1.6 %), and no visible cracks were successfully created. The LBW process demonstrated effective low-heat input characteristics, evident from a considerably narrow heat-affected zone (HAZ). Control over FZ width and grain size was achieved, measuring 600 and 112 µm at low welding speed and 250 and 49 µm at high welding speed, respectively, significantly lower than previous studies. A remarkably high yield strength (YS) of ∼620 MPa and ultimate tensile strength (UTS) up to 845 MPa were observed in the as-welded conditions, improving to ∼645 and 875 MPa, respectively, after PWHT. This enhancement in mechanical properties is primarily attributed to lattice friction induced by V addition. PWHT also improved joint ductility, increasing from 3.5 % to 8.6 % (low-speed) and from 6.3 % to 9.2 % (high-speed). The reduction in crystallographic orientation achieved using a higher welding speed and PWHT emerged as a major reason for improved mechanical properties. Slip-based deformation mechanisms dominated across all conditions, featuring crystallographically aligned slip bands. Interactions between existing and additional slip bands formed a dense dislocation network crucial for enhanced elongation after PWHT. Thermodynamic parameters elucidating phase stability in the observed FZs and contributions to superior YS were calculated and comprehensively discussed.展开更多
This study comprehensively investigates the effects of annealing on the structural,electrochemical properties and passivation film characteristics of Ti_(20)Zr_(20)Hf_(20)Be_(20)Ni_(20)(at%)high-entropy metallic glass...This study comprehensively investigates the effects of annealing on the structural,electrochemical properties and passivation film characteristics of Ti_(20)Zr_(20)Hf_(20)Be_(20)Ni_(20)(at%)high-entropy metallic glass(HE-MG).Subjected to various annealing temperatures,the samples were analyzed in a 3.5 wt%NaCl solution to evaluate changes in their microstructure and assess their corrosion resistance.Findings reveal that the HE-MG undergoes multistage crystallization,displaying an amorphous matrix integrated with face centered cubic(FCC)and Ni_(7)Zr_(2)phases between 420 and 500℃,indicating robust thermal stability.Electrochemical assessments identify a critical temperature threshold:Below the glass transition temperature(Tg),the HE-MG maintains excellent corrosion resistance,promoting stable passivation layers.Above Tg,enhanced long-range atomic rearrangement during relaxation increases passivation layer defects and significantly diminishes corrosion resistance.X-ray photoelectron spectroscopy(XPS)analyses show that the primary components of the passivation layer are TiO_(2),ZrO_(2),HfO_(2)and BeO.Increased annealing temperatures lead to enhanced Be and Ni content and decreased Ti,Zr and Hf.Additionally,high mixing entropy and significant atomic size mismatch suppress long-range atomic rearrangement and crystallization.The crystallization begins above Tg by_(20)℃,with crystalline phases evenly distributed within the matrix without drastically affecting corrosion resistance.This investigation highlights the impact of thermal treatment on the properties of HE-MG,contributing valuable insights into optimizing their performance and applications.展开更多
Pure Mg boasting a relatively small corrosion rate is a potential biodegradable metal material for implants.However,its degradation behavior in the complex physiological environment is still a lack of understanding.In...Pure Mg boasting a relatively small corrosion rate is a potential biodegradable metal material for implants.However,its degradation behavior in the complex physiological environment is still a lack of understanding.In this work,we investigated the effect of corrosion product film layers on the degradation behavior of pure Mg in physiological environments.Pure Mg shows a faster corrosion rate in simulated body fluid(SBF)compared to NaCl solution.Hydrogen evolution experiments indicate that the degradation rate of pure Mg in SBF decreases rapidly within the first 12 h but stabilizes afterward.The rapid deposition of low-solubility calcium phosphate on the pure Mg in SBF provides protection to the substrate,resulting in a gradual decrease in the degradation rates.Consequently,the corrosion product film of pure Mg formed in SBF exhibits a layered structure,with the upper layer consisting of dense Ca_(3)(PO_(4))_(2)/Mg_(3)(PO_(4))_(2) and the lower layer consisting of Mg(OH)_(2)/MgO.Electrochemical impedance spectroscopy(EIS)shows that the resistance of the corrosion product film increases over time,indicating gradual strengthening of the corrosion resistance.The 4-week degradation results in the femoral marrow cavity of mice are consistent with the result in SBF in vitro.展开更多
Al_(2)O_(3)and MgO serve as the primary gangue components in sintered ores,and they are critical for the formation of CaO-Fe_(2)O_(3)-xAl_(2)O_(3)(wt%,C-F-xA)and CaO-Fe_(2)O_(3)-xM gO(wt%,C-F-xM)systems,respectively.I...Al_(2)O_(3)and MgO serve as the primary gangue components in sintered ores,and they are critical for the formation of CaO-Fe_(2)O_(3)-xAl_(2)O_(3)(wt%,C-F-xA)and CaO-Fe_(2)O_(3)-xM gO(wt%,C-F-xM)systems,respectively.In this study,a nonisothermal crystallization thermodynamics behavior of C-F-xA and C-F-xM systems was examined using differential scanning calorimetry,and a phase identification and microstructure analysis for C-F-xA and C-F-xM systems were carried out by X-ray diffraction and scanning electron microscopy.Results showed that in C-F-2A and C-F-2M systems,the increased cooling rates promoted the precipitation of CaFe_(2)O_(4)(CF)but inhibited the formation of Ca_(2)Fe_(2)O_(5)(C2F).In addition,C-F-2A system exhibited a lower theoretical initial crystallization temperature(1566 K)compared to the C-F system(1578 K).This temperature further decreases to 1554 K and 1528 K in the C-F-4A and C-F-8A systems,respectively.However,in C-F-xM system,the increased MgO content raised the crystallization temperature.This is because that the enhanced precipitation of MF(a spinel phase mainly comprised Fe_(3)O_(4)and MgFe_(2)O_(4))and C2F phases suppressed the CF precipitation reaction.In kinetic calculations,the Ozawa method revealed the apparent activation energies of the C-F-2A and C-F-2M systems.Malek's method revealed that the crystallization process in C-F-2A system initially followed a logarithmic law(lnαor lnα2),later transitioning to a reaction order law((1-α)-1or(1-α)^(-1/2),n=2/3)or the lnα2function of the exponential law.In C-F-2M system,it consistently followed the sequencef(α)=(1-α)^(2)(αis the crystallization conversion rate;n is the Avrami constant;?(α)is the differential equations for the model function of C_(2)F and CF crystallization processes).展开更多
Engineering point defects such as metal and oxygen vacancies play a crucial role in manipulating the electrical,optical,and catalytic properties of oxide semiconductors for solar water splitting.Herein,we synthesized ...Engineering point defects such as metal and oxygen vacancies play a crucial role in manipulating the electrical,optical,and catalytic properties of oxide semiconductors for solar water splitting.Herein,we synthesized nanoporous CuBi_(2)O_(4)(np-CBO)photocathodes and engineered their surface point defects via rapid thermal processing(RTP)in controlled atmospheres(O_(2),N_(2),and vacuum).We found that the O_(2)-RTP treatment of np-CBO increased the charge carrier density effectively without hampering the nanoporous morphology,which was attributed to the formation of copper vacancies(VCu).Further analyses revealed that the amounts of oxygen vacancies(Vo)and Cu^(1+)were reduced simultaneously,and the relative electrochemical active surface area increased after the O_(2)-RTP treatment.Notably,the point defects(VC_(u),Cu^(1+),and Vo)regulated np-CBO achieved a superb water-splitting photocurrent density of-1.81 m A cm^(-2) under simulated sunlight illumination,which is attributed to the enhanced charge transport and transfer properties resulting from the regulated surface point defects.Finally,the reversibility of the formation of the point defects was checked by sequential RTP treatments(O_(2)-N_(2)-O_(2)-N_(2)),demonstrating the strong dependence of photocurrent response on the RTP cycles.Conclusively,the surface point defect engineering via RTP treatment in a controlled atmosphere is a rapid and facile strategy to promote charge transport and transfer properties of photoelectrodes for efficient solar water-splitting.展开更多
The corrosion rates of additive-manufactured Mg alloys are higher than their as-cast counterparts,possibly due to increased kinetics for the hydrogen evolution reaction on secondary phases,which may include oxide incl...The corrosion rates of additive-manufactured Mg alloys are higher than their as-cast counterparts,possibly due to increased kinetics for the hydrogen evolution reaction on secondary phases,which may include oxide inclusions.Scanning Kelvin Probe Force Microscopy demonstrated that MgO inclusions could act as cathodes for Mg corrosion,but their low conductivity likely precludes this.However,the density of state calculations through density functional theory using hybrid HSE06 functional revealed overlapping electronic states at the Mg/MgO interface,which facilitates electron transfers and participates in redox reactions.Subsequent determination of the hydrogen absorption energy at the Mg/MgO interface reveals it to be an excellent catalytic site,with HER being found to be a factor of 23x more efficient at the interface than on metallic Mg.The results not only support the plausibility of the Mg/MgO interface being an effective cathode to the adjacent anodic Mg matrix during corrosion but also contribute to the understanding of the enhanced cathodic activities observed during the anodic dissolution of magnesium.展开更多
Since topological quantum materials may possess interesting properties and promote the application of electronic devices,the search for new topological quantum materials has become the focus and frontier of condensed ...Since topological quantum materials may possess interesting properties and promote the application of electronic devices,the search for new topological quantum materials has become the focus and frontier of condensed matter physics.Currently,it has been found that there are two interesting systems in topological quantum materials:topological superconducting materials and topological magnetic materials.Although research on these materials has made rapid progress,a systematic review of their synthesis,properties,and applications,particularly their synthesis,is still lacking.In this paper,we emphasize the experimental preparation of two typical topological quantum materials and then briefly introduce their potential physical properties and applications.Finally,we provide insights into current and future issues in the study of topological quantum material systems.展开更多
This study demonstrates that two-and three-dimensional spatially graded,truss-based polymeric-material metamaterials can be designed for beneficial impact mitigation and energy absorption capabilities.Through a combin...This study demonstrates that two-and three-dimensional spatially graded,truss-based polymeric-material metamaterials can be designed for beneficial impact mitigation and energy absorption capabilities.Through a combination of numerical and experimental techniques,we highlight the broad property space of periodic viscoelastic trusses,realized using 3D printing via selective laser sintering.Extending beyond periodic designs,we investigate the impact response of spatially variant viscoelastic lattices in both two and three dimensions.Our result reveal that introducing spatial variations in lattice topology allows for redirecting of the impact trajectory,opening new opportunities for engineering and tailoring lightweight materials with target impact functionality.This is achieved through the combined selection of base material and metamaterial design.展开更多
This study investigates the influence of CaO(0.5,1(wt.%))alloying on the microstructural evolution,texture development and deformation behavior of AZ61 magnesium alloy.The uniaxial tension tests at room(RT)and cryogen...This study investigates the influence of CaO(0.5,1(wt.%))alloying on the microstructural evolution,texture development and deformation behavior of AZ61 magnesium alloy.The uniaxial tension tests at room(RT)and cryogenic(CT,-150℃)temperature were performed to investigate the twinability and dislocation behavior and its consequent effect on flow stress,ductility and strain hardening rate.The results showed that the AZ61-1CaO exhibited superior strength/ductility synergy at RT with a yield strength(YS)of 223 MPa and a ductility of 23% as compared to AZ61(178 MPa,18.5%)and AZ61-0.5CaO(198 MPa,21%).Similar trend was witnessed for all the samples during CT deformation,where increase in the YS and decrease in ductility were observed.The Mtex tools based in-grain misorientation axis(IGMA)analysis of RT deformed samples revealed the higher activities of prismatic slip in AZ61-CaO,which led to superior ductility.Moreover,subsequent EBSD analysis of CT deformed samples showed the increased fraction of fine{10-12}tension twins and nucleation of multiple{10-12}twin variants caused by higher local stress concentration at the grain boundaries,which imposed the strengthening by twin-twin interaction.Lastly,the detailed investigations on strengthening contributors showed that the dislocation strengthening has the highest contribution towards strength in all samples.展开更多
Although hydrofluoric acid(HF)surface treatment is known to enhance the joining of metals with polymers,there is limited information on its effect on the joining of AZ31 alloy and carbon-fiber-reinforced plastics(CFRP...Although hydrofluoric acid(HF)surface treatment is known to enhance the joining of metals with polymers,there is limited information on its effect on the joining of AZ31 alloy and carbon-fiber-reinforced plastics(CFRPs)through laser-assisted metal and plastic direct joining(LAMP).This study uses the LAMP technique to produce AZ31-CFRP joints.The joining process involves as-received AZ31,HFpretreated AZ31,and thermally oxidized HF-pretreated AZ31 alloy sheets.Furthermore,the bonding strength of joints prepared with thermally oxidized AZ31 alloy sheets is examined to ascertain the combined effect of HF treatment and thermal oxidation on bonding strength.The microstructures,surface chemical interactions,and mechanical performances of joints are investigated under tensile shear loading.Various factors,such as bubble formation,CFRP resin decomposition,and mechanical interlocking considerably affect joint strength.Additionally,surface chemical interactions between the active species on metal parts and the polar amide along with carbonyl groups of polymer play a significant role in improving joint strength.Joints prepared with surface-pretreated AZ31 alloy sheets show significant improvements in bonding strength.展开更多
In the present research,the NaF assisted plasma electrolytic oxidation(PEO)is designed to fabricate the high-content ZnO nanoparti-cles doped coating on AZ31B alloy.The microstructure,phase constituents and corrosion ...In the present research,the NaF assisted plasma electrolytic oxidation(PEO)is designed to fabricate the high-content ZnO nanoparti-cles doped coating on AZ31B alloy.The microstructure,phase constituents and corrosion behavior of the PEO coatings are investigated systematically.The results reveal that the introduction of NaF promotes the formation of MgF2 nanophases in the passivation layer on Mg alloy,decreasing the breakdown voltage and discharge voltage.As a result,the continuous arcing caused by high discharge voltage is alleviated.With the increasing of NaF content,the Zn content in the PEO coating is enhanced and the pore size in the coating is decreased correspondingly.Due to the high-content ZnO doping,the PEO coating protected AZ31B alloy demonstrates the better corrosion resistance.Compared with the bare AZ31B alloy,the high-content ZnO doped PEO coated sample shows an increased corrosion potential from-1.465 V to-1.008 V,a decreased corrosion current density from 3.043×10^(-5) A·cm^(-2) to 3.960×10^(-8) A·cm^(-2) and an increased charge transfer resistance from 1.213×10^(2) ohm·cm^(2) to 2.598×10^(5) ohm·cm^(2).Besides,the high-content ZnO doped PEO coated sample also has the excellent corrosion resistance in salt solution,exhibiting no obvious corrosion after more than 2000 h neutral salt spraying and 28 days’immersion testing.The improved corrosion resistance can be ascribed to the relative uniform distribution of ZnO in PEO coating which can transform to Zn(OH)2 and form a continuous protective layer along the corrosion interface.展开更多
Electrochemical nitrate reduction(ENR)is an economical and eco-friendly method for converting industrial wastewater into valuable ammonia under atmospheric conditions.The main challenge lies in designing and developin...Electrochemical nitrate reduction(ENR)is an economical and eco-friendly method for converting industrial wastewater into valuable ammonia under atmospheric conditions.The main challenge lies in designing and developing highly durable ENR electrocatalysts.This study introduces defect-rich mesoporous CuO_(x) nanowires electrocatalyst synthesized using a novel solution-flame(sol-flame)hybrid method to control mesoporosity and introduce surface defects,thereby enhancing the electrochemical nitrate-toammonia production performance.We found surface defects(oxygen vacancies and Cu^(+))and unique mesoporous nanowire structure composed of tightly interconnected nanoparticles.The sol-flamesynthesized CuO_(x) nanowires(sf-CuO NWs)achieved superior ammonia yield rate(0.51 mmol h^(-1)cm^(-2)),faradaic efficiency(97.3%),and selectivity(86.2%)in 1 M KOH electrolyte(2000 ppm nitrate).This performance surpasses that of non-porous and less-defective CuO NWs and is attributed to the increased surface area and rapid electron transport facilitated by the distinctive morphology and generated defects.Theoretical calculation further suggests oxygen vacancies enhance NO_(3)^(-)adsorption on the sf-CuO NWs’surface and mitigate the competing hydrogen evolution reaction.This study outlines a strategic design and simple synthesis approach for nanowire electrocatalysts that boost the efficiency of electrochemical nitrate-to-ammonia conversion.展开更多
Immersion of scaffolds in Simulated Body Fluid(10SBF)is a standardized method for evaluating their bioactivity,simulating in vivo conditions where apatite deposits can be formed on the surface of scaffold,facilitating...Immersion of scaffolds in Simulated Body Fluid(10SBF)is a standardized method for evaluating their bioactivity,simulating in vivo conditions where apatite deposits can be formed on the surface of scaffold,facilitating bone integration and ensuring their suitability for bone implant purposes,ultimately contributing to long-term implant success.The effect of apatite deposition on bioactivity and cell behavior of TiO_(2)scaffolds was studied.Scaffolds were soaked in 10SBF for different durations to form HAP layer on their surface.The results proved the development of a hydroxyapatite film resembling the mineral composition of bone Extracellular Matrix(ECM)on the TiO_(2)scaffolds.The XRD test findings showed the presence of hydroxyapatite layer similar to bone at the depth of 10 nm.A decrease in the specific surface area(18.913 m^(2)g^(−1)),the total pore volume(0.045172 cm^(3)g^(−1)(at p/p0=0.990)),and the mean pore diameter(9.5537 nm),were observed by BET analysis which confirmed the formation of the apatite layer.It was found that titania scaffolds with HAP coating promoted human osteosarcoma bone cell(MG63)cell attachment and growth.It seems that immersing the scaffolds in 10SBF to form HAP coating before utilizing them for bone tissue engineering applications might be a good strategy to promote bioactivity,cell attachment,and implant fixation.展开更多
Single-phase face-centered cubic(fcc)high/medium-entropy alloys(H/MEAs)exhibit a much higher tendency to form nanoscale deformation twins than conventional fcc metals with similar low stacking fault energies(SFEs).Thi...Single-phase face-centered cubic(fcc)high/medium-entropy alloys(H/MEAs)exhibit a much higher tendency to form nanoscale deformation twins than conventional fcc metals with similar low stacking fault energies(SFEs).This extraordinary propensity for nanotwin formation in H/MEAs cannot therefore be ex-plained by their low SFEs alone.Here,using in situ compression tests of CrCoNi in comparison with Ag nanopillars inside a transmission electron microscope,we found that in the CrCoNi MEA,a high density of nanoscale twins continuously formed with an average thickness of 4.6 nm.In contrast,for similar experiments on Ag with almost identical SFE,following the nucleation of a few twins,they could further thicken to above one hundred nanometers by twin boundary migration.Molecular dynamics calculations indicated that in the highly-concentrated CrCoNi solid solution,the magnitude of the energy barriers for nucleating a stacking fault as a twin precursor in the pristine lattice and for the thickening of an existing twin both span a wide range and largely overlap with each other.Therefore,twin thickening through successive addition of atomic layers is prone to discontinuation,giving way to the nucleation of new twins at other sites where a lower energy barrier is encountered for partial-dislocation mediated fault formation.展开更多
As implanted bone fixation materials,magnesium(Mg)alloys have significant advantages because the density and elastic modulus are closest to those of the human bone and they can bio-degrade in the physiological environ...As implanted bone fixation materials,magnesium(Mg)alloys have significant advantages because the density and elastic modulus are closest to those of the human bone and they can bio-degrade in the physiological environment.However,Mg alloys degrade too rapidly and uncontrollably thus hampering clinical adoption.In this study,a highly corrosion-resistant zinc-phosphate-doped micro-arc oxidation(MAO)coating is prepared on the AZ31B alloy,and the degradation process is assessed in vitro.With increasing zinc phosphate concentrations,both the corrosion potentials and charge transfer resistance of the AZ31B alloy coated with MAO coatings increase gradually,while the corrosion current densities di-minish gradually.Immersion tests in the simulated body fluid(SBF)reveal that the increased zinc phos-phate concentration in MAO coating decreases the degradation rate,consequently reducing the release rates of Mg^(2+)and OH-in the physiological micro-environment,which obtains the lowest weight loss of only 5.22%after immersion for 56 days.Effective regulation of degradation provides a weak alkaline environment that is suitable for long-term cell growth and subsequent promotion of bone proliferation,differentiation,mineralization,and cytocompatibility.In addition,the zinc-phosphate-doped MAO coat-ings show an improved wear resistance as manifested by a wear rate of only 3.81 x 10^(-5) mm^(3) N^(-1) m^(-1).The results reveal a suitable strategy to improve the properties of biodegradable Mg alloys to balance tissue healing with mechanical degradation.展开更多
Achieving a delicate synergy between mechanical robustness and antifouling attributes in coatings remains a formidable challenge for marine applications. Inspired by the assembly of nacre, we present a novel approach ...Achieving a delicate synergy between mechanical robustness and antifouling attributes in coatings remains a formidable challenge for marine applications. Inspired by the assembly of nacre, we present a novel approach to fabricate a nacre-like metallic coating. This coating comprises an amorphous matrix with excellent anti-corrosion and anti-wear properties, as well as Cu-rich 3D interconnected channels for antifouling function. The coating is produced by high velocity oxygen fuel (HVOF) thermal spraying of surface-modified Fe-based amorphous powders with a Cu-layer. The resulting coating exhibits exceptional mechanical robustness, including high resistance to erosion, abrasion, and impact, surpassing conventional polymer antifouling coatings. Furthermore, the controlled Cu+ leaching capability of the in-situ constructed 3D interconnected diffusion channels, facilitated by the Cu-rich intersplats, contributes to the remarkable antifouling performance. This includes nearly 100 % resistance to bacterial adhesion after 1 day of immersion and over 98 % resistance to algal attachment after 7 d of immersion, resulting in a prolonged service lifetime. Notably, even after 200 cycles of wear damage, the Cu-modified amorphous coating still maintains its excellent antifouling properties. The Cu-rich intersplats play a critical role in transporting and sustainably leaching Cu ions, thereby accounting for the outstanding antifouling performance. Ultimately, we aim to advance the design of high-performance coatings suited for diverse marine applications, where both the mechanical robustness and antifouling properties are essential.展开更多
With the gradual reduction in high-quality iron ore resources,the global steel industry faces long-term challenges.For example,the continuous increase in the Al_(2)O_(3) content of iron ore has led to a decrease in th...With the gradual reduction in high-quality iron ore resources,the global steel industry faces long-term challenges.For example,the continuous increase in the Al_(2)O_(3) content of iron ore has led to a decrease in the metallurgical performance of sinter and fluctuations in slag properties.Considering calcium ferrite(CF)and composite CF(silico-ferrite of calcium and aluminum,SFCA)play a crucial role as a binding phase in high-alkalinity sinter and exhibit excellent physical strength and metallurgical performance,we propose incorporating excess Al_(2)O_(3) into SFCA to form a new binding phase with excellent properties for high-quality sinter preparation.In the synthesis of high-Al_(2)O_(3) SFCA,two high-Al_(2)O_(3) phases were identified as types A(Al_(1.2)Ca_(2.8)Fe_(8.7)O_(2)0Si_(0.8))and B(Ca_(4)Al_(4.18)Fe_(1.82)Si_(6)O_(26)).Results show that type A SFCA sample had a higher cell density(4.13 g/cm^(3))and longer Fe-O bond length(2.2193Å)than type B(3.46 g/cm^(3) and 1.9415Å),with a significantly greater lattice oxygen concentration(7.86%vs.1.85%),which demonstrates advantages in strength and reducibility.Type A SFCA sample contained a lower proportion of silicates,was predominantly composed of SFCA,and exhibited minimal porosity.Melting point and viscosity simulation tests indicate that type A SFCA sample formed a liquid phase at 880°C with a viscosity range of 0-0.35 Pa·s,which is notably lower than that of type B SFCA sample(1220°C and 0-20 Pa·s).This finding suggests that type A SFCA sample has a low initial melting temperature and viscosity,which facilitates increasing liquid-phase generation and improving flow properties.Such a condition enhances the adhesion to surrounding ore particles.Compressive strength tests reveal that type A SFCA sample(36.83-42.48 MPa)considerably outperformed type B SFCA sample(5.98-12.79 MPa)and traditional sinter(5.02-13.68 MPa).In addition,at 900°C,type A SFCA sample achieved a final reducibility of 0.89,which surpassed that of type B SFCA sample(0.83).In summary,type A SFCA sample demonstrates superior structural,thermophysical,and metallurgical properties,which highlights its promising potential for industrial applications.展开更多
Artificial Intelligence(AI)has revolutionized technological development globally,delivering relatively more accurate and reliable solutions to critical challenges across various research domains.This impact is particu...Artificial Intelligence(AI)has revolutionized technological development globally,delivering relatively more accurate and reliable solutions to critical challenges across various research domains.This impact is particularly notable within the field of materials science and engineering,where artificial intelligence has catalyzed the discovery of new materials,enhanced design simulations,influenced process controls,and facilitated operational analysis and predictions of material properties and behaviors.Consequently,these advancements have stream-lined the synthesis,simulation,and processing procedures,leading to material optimization for diverse appli-cations.A key area of interest within materials science is the development of hydrogen-based electrochemical systems,such as fuel cells and electrolyzers,as clean energy solutions,known for their promising high energy density and zero-emission operations.While artificial intelligence shows great potential in studying both fuel cells and electrolyzers,existing literature often separates them,with a clear gap in comprehensive studies on electrolyzers despite their similarities.This review aims to bridge that gap by providing an integrated overview of artificial intelligence’s role in both technologies.This review begins by explaining the fundamental concepts of artificial intelligence and introducing commonly used artificial intelligence-based algorithms in a simplified and clearly comprehensible way,establishing a foundational knowledge base for further discussion.Subsequently,it explores the role of artificial intelligence in materials science,highlighting the critical applications and drawing on examples from recent literature to build on the discussion.The paper then examines how artificial intelligence has propelled significant advancements in studying various types of fuel cells and electrolyzers,specifically emphasizing proton exchange membrane(PEM)based systems.It thoroughly explores the artificial intelligence tools and techniques for characterizing,manufacturing,testing,analyzing,and optimizing these systems.Additionally,the review critically evaluates the current research landscape,pinpointing progress and prevailing challenges.Through this thorough analysis,the review underscores the fundamental role of artificial intelligence in advancing the generation and utilization of clean energy,illustrating its transformative potential in this area of research.展开更多
基金supported by the National Research Foundation of Korea(NRF)grant fu nded by the Korean government(MSIT)(No.RS-2024-00335976)。
文摘Antimony sulfide(Sb_(2)S_(3))is a promising material for photoelectrochemical(PEC)devices that generate green hydrogen from sunlight and water.In this study,we present a synthesis of high-performance Sb_(2)S_(3)photoanodes via an interface-engineered hydrothermal growth followed by rapid thermal annealing(RTA).A TiO_(2)interfacial layer plays a crucial role in ensuring homogeneous precursor deposition,enhancing light absorption,and forming efficient heterojunctions with Sb_(2)S_(3),thereby significantly improving charge separation and transport.RTA further improves crystallinity and interfacial contact,resulting in dense and uniform Sb_(2)S_(3)films with enlarged grains and fewer defects.The optimized Sb_(2)S_(3)photoanode achieves a photocurrent density of 2.51 mA/cm^(2)at 1.23 V vs.the reversible hydrogen electrode(RHE),one of the highest reported for Sb_(2)S_(3)without additional catalysts or passivation layers.To overcome the limitations of oxygen evolution reaction(OER),we employ the iodide oxidation reaction(IOR)as an alternative,significantly lowering the overpotential and improving charge transfer kinetics.Consequently,it produces a record photocurrent density of 8.9 mA/cm^(2)at 0.54 V vs.RHE.This work highlights the synergy between TiO_(2)interfacial engineering,RTA-induced crystallization,and IOR-driven oxidation,offering a promising pathway for efficient and scalable PEC hydrogen production.
基金supported by the U.S.Department of Energy’s Office of Energy Efficiency and Renewable Energy(EERE)under the Advanced Manufacturing Office Award Number DE-EE0007897。
文摘In secondary Al-Si based alloys,microalloying with Mn and Cr can modify harmful platelet-type Alx Fey Siz intermetallic phases to less detrimentalα-Alx(Fe,Mn,Cr)_(y)Siz phase(script or polygonal morphologies).However,theα-Alx(Fe,Mn,Cr)_(y)Siz phase morphology,phase composition and the addition of Fecorrecting elements can be influenced by solidification conditions.Therefore,this research is aimed to highlight the morphological evolution and mechanisms ofα-Alx(Fe,Mn,Cr)_(y)Si_(z)phase in a Cr added Al-9%Si-1%Fe-0.2%Cr(all weight percentage thereafter,unless otherwise stated)alloy with varying Mn concentrations(0.25%,0.5%,and 0.8%).Microstructure evolution of Fe intermetallic phases is investi-gated under different casting conditions using a wedge-shaped die,Cu-chill block and melt quenching experiments.Thermodynamic simulations have been performed using CALculation of PHAse Diagrams(CALPHAD)method and compared with the experimental results for phase composition and formation temperatures ofα-Alx(Fe,Mn,Cr)_(y)Siz phase.The results indicated that for 0.25Mn-0.2Cr addition to Al-9Si-1Fe alloy,compact morphology containing polygonal phases are formed in Cu-chill casting,while the wedge castings predominantly show a mixed structure with platelets and script type morphologies.Tensile tests revealed a higher elongation value of 6.6%for mixed structure with platelet and script phases,which is decreased to 4.2%for polygonal phases in Al-9Si-1Fe-0.2Cr-0.25Mn alloy.This study highlights the importance of solidification conditions on morphologies of Fe-intermetallic phases and the mechanical properties by comparing selected literature relevant to high pressure die-casting process.
基金supported by the Nano&Material Technology Development Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Science and ICT(Nos.RS-2023-00234757 and RS-2024-00402289)。
文摘In engineering structures, the application of advanced alloys, such as the VCoNi medium-entropy alloy (VCoNi-MEA), with remarkable tensile strength (> 1 GPa) and superior ductility necessitates the employment of dissimilar joints. This study pioneers the dissimilar joining of VCoNi-MEA and 17–4 precipitation hardening stainless steel (17–4PH STS) using state-of-the-art green laser beam welding (LBW). To evaluate and optimize the experimental parameters, two welding speeds (200 and 300 mm/s) along with post-weld heat treatment (PWHT) were incorporated. High-quality welded joints with a single-phase face-centered cubic (FCC) structure in the fusion zone (FZ), minimal precipitates (< 1.6 %), and no visible cracks were successfully created. The LBW process demonstrated effective low-heat input characteristics, evident from a considerably narrow heat-affected zone (HAZ). Control over FZ width and grain size was achieved, measuring 600 and 112 µm at low welding speed and 250 and 49 µm at high welding speed, respectively, significantly lower than previous studies. A remarkably high yield strength (YS) of ∼620 MPa and ultimate tensile strength (UTS) up to 845 MPa were observed in the as-welded conditions, improving to ∼645 and 875 MPa, respectively, after PWHT. This enhancement in mechanical properties is primarily attributed to lattice friction induced by V addition. PWHT also improved joint ductility, increasing from 3.5 % to 8.6 % (low-speed) and from 6.3 % to 9.2 % (high-speed). The reduction in crystallographic orientation achieved using a higher welding speed and PWHT emerged as a major reason for improved mechanical properties. Slip-based deformation mechanisms dominated across all conditions, featuring crystallographically aligned slip bands. Interactions between existing and additional slip bands formed a dense dislocation network crucial for enhanced elongation after PWHT. Thermodynamic parameters elucidating phase stability in the observed FZs and contributions to superior YS were calculated and comprehensively discussed.
基金supported by the National Key R&D Program of China(No.2021YFE0100600)the National Natural Science Foundation of China(No.52371154)+2 种基金Guangdong Basic and Applied Basic Research Foundation(No.2023A1515012158)the Opening Project of the Key Laboratory of CNC Equipment Reliability,Ministry of Education,Jilin University(No.JLU-cncr-202307)the Knowledge Innovation Program of Wuhan-Basic Research(No.2022010801010087).
文摘This study comprehensively investigates the effects of annealing on the structural,electrochemical properties and passivation film characteristics of Ti_(20)Zr_(20)Hf_(20)Be_(20)Ni_(20)(at%)high-entropy metallic glass(HE-MG).Subjected to various annealing temperatures,the samples were analyzed in a 3.5 wt%NaCl solution to evaluate changes in their microstructure and assess their corrosion resistance.Findings reveal that the HE-MG undergoes multistage crystallization,displaying an amorphous matrix integrated with face centered cubic(FCC)and Ni_(7)Zr_(2)phases between 420 and 500℃,indicating robust thermal stability.Electrochemical assessments identify a critical temperature threshold:Below the glass transition temperature(Tg),the HE-MG maintains excellent corrosion resistance,promoting stable passivation layers.Above Tg,enhanced long-range atomic rearrangement during relaxation increases passivation layer defects and significantly diminishes corrosion resistance.X-ray photoelectron spectroscopy(XPS)analyses show that the primary components of the passivation layer are TiO_(2),ZrO_(2),HfO_(2)and BeO.Increased annealing temperatures lead to enhanced Be and Ni content and decreased Ti,Zr and Hf.Additionally,high mixing entropy and significant atomic size mismatch suppress long-range atomic rearrangement and crystallization.The crystallization begins above Tg by_(20)℃,with crystalline phases evenly distributed within the matrix without drastically affecting corrosion resistance.This investigation highlights the impact of thermal treatment on the properties of HE-MG,contributing valuable insights into optimizing their performance and applications.
基金supported by the National Natural Science Foundation of China(52127801)Postdoctoral Fellowship Program of CPSF under Grant Number GZC20231545,China Postdoctoral Science Foundation(2024T170557 and 2023M742224)+1 种基金Shanghai Post-doctoral Excellence Program(No.2023440)City University of Hong Kong Donation Grants(DON-RMG No.9229021 and 9220061).
文摘Pure Mg boasting a relatively small corrosion rate is a potential biodegradable metal material for implants.However,its degradation behavior in the complex physiological environment is still a lack of understanding.In this work,we investigated the effect of corrosion product film layers on the degradation behavior of pure Mg in physiological environments.Pure Mg shows a faster corrosion rate in simulated body fluid(SBF)compared to NaCl solution.Hydrogen evolution experiments indicate that the degradation rate of pure Mg in SBF decreases rapidly within the first 12 h but stabilizes afterward.The rapid deposition of low-solubility calcium phosphate on the pure Mg in SBF provides protection to the substrate,resulting in a gradual decrease in the degradation rates.Consequently,the corrosion product film of pure Mg formed in SBF exhibits a layered structure,with the upper layer consisting of dense Ca_(3)(PO_(4))_(2)/Mg_(3)(PO_(4))_(2) and the lower layer consisting of Mg(OH)_(2)/MgO.Electrochemical impedance spectroscopy(EIS)shows that the resistance of the corrosion product film increases over time,indicating gradual strengthening of the corrosion resistance.The 4-week degradation results in the femoral marrow cavity of mice are consistent with the result in SBF in vitro.
基金financially supported by the National Natural Science Foundation of China(Nos.52204331 and 52374315)the Major Industrial Innovation Plan of Anhui Provincial Development and the Reform Commission,China(No.AHZDCYCX-LSDT2023-01)。
文摘Al_(2)O_(3)and MgO serve as the primary gangue components in sintered ores,and they are critical for the formation of CaO-Fe_(2)O_(3)-xAl_(2)O_(3)(wt%,C-F-xA)and CaO-Fe_(2)O_(3)-xM gO(wt%,C-F-xM)systems,respectively.In this study,a nonisothermal crystallization thermodynamics behavior of C-F-xA and C-F-xM systems was examined using differential scanning calorimetry,and a phase identification and microstructure analysis for C-F-xA and C-F-xM systems were carried out by X-ray diffraction and scanning electron microscopy.Results showed that in C-F-2A and C-F-2M systems,the increased cooling rates promoted the precipitation of CaFe_(2)O_(4)(CF)but inhibited the formation of Ca_(2)Fe_(2)O_(5)(C2F).In addition,C-F-2A system exhibited a lower theoretical initial crystallization temperature(1566 K)compared to the C-F system(1578 K).This temperature further decreases to 1554 K and 1528 K in the C-F-4A and C-F-8A systems,respectively.However,in C-F-xM system,the increased MgO content raised the crystallization temperature.This is because that the enhanced precipitation of MF(a spinel phase mainly comprised Fe_(3)O_(4)and MgFe_(2)O_(4))and C2F phases suppressed the CF precipitation reaction.In kinetic calculations,the Ozawa method revealed the apparent activation energies of the C-F-2A and C-F-2M systems.Malek's method revealed that the crystallization process in C-F-2A system initially followed a logarithmic law(lnαor lnα2),later transitioning to a reaction order law((1-α)-1or(1-α)^(-1/2),n=2/3)or the lnα2function of the exponential law.In C-F-2M system,it consistently followed the sequencef(α)=(1-α)^(2)(αis the crystallization conversion rate;n is the Avrami constant;?(α)is the differential equations for the model function of C_(2)F and CF crystallization processes).
基金supported by the Basic Science Research Program through the National Research Foundation of Korea,funded by the Ministry of Science,ICT,and Future Planning(NRF Award No.NRF-2019R1A2C2002024 and 2021R1A4A1031357)supported by the Basic Science Research Program through NRF funded by the Ministry of Education(NRF Award No.NRF2020R1A6A1A03043435)。
文摘Engineering point defects such as metal and oxygen vacancies play a crucial role in manipulating the electrical,optical,and catalytic properties of oxide semiconductors for solar water splitting.Herein,we synthesized nanoporous CuBi_(2)O_(4)(np-CBO)photocathodes and engineered their surface point defects via rapid thermal processing(RTP)in controlled atmospheres(O_(2),N_(2),and vacuum).We found that the O_(2)-RTP treatment of np-CBO increased the charge carrier density effectively without hampering the nanoporous morphology,which was attributed to the formation of copper vacancies(VCu).Further analyses revealed that the amounts of oxygen vacancies(Vo)and Cu^(1+)were reduced simultaneously,and the relative electrochemical active surface area increased after the O_(2)-RTP treatment.Notably,the point defects(VC_(u),Cu^(1+),and Vo)regulated np-CBO achieved a superb water-splitting photocurrent density of-1.81 m A cm^(-2) under simulated sunlight illumination,which is attributed to the enhanced charge transport and transfer properties resulting from the regulated surface point defects.Finally,the reversibility of the formation of the point defects was checked by sequential RTP treatments(O_(2)-N_(2)-O_(2)-N_(2)),demonstrating the strong dependence of photocurrent response on the RTP cycles.Conclusively,the surface point defect engineering via RTP treatment in a controlled atmosphere is a rapid and facile strategy to promote charge transport and transfer properties of photoelectrodes for efficient solar water-splitting.
基金Agency for Science,Technology and Research(A*STAR),under the RIE2020 Advanced Manufacturing and Engineering(AME)Programmatic Grant(Grant no.A18B1b0061)。
文摘The corrosion rates of additive-manufactured Mg alloys are higher than their as-cast counterparts,possibly due to increased kinetics for the hydrogen evolution reaction on secondary phases,which may include oxide inclusions.Scanning Kelvin Probe Force Microscopy demonstrated that MgO inclusions could act as cathodes for Mg corrosion,but their low conductivity likely precludes this.However,the density of state calculations through density functional theory using hybrid HSE06 functional revealed overlapping electronic states at the Mg/MgO interface,which facilitates electron transfers and participates in redox reactions.Subsequent determination of the hydrogen absorption energy at the Mg/MgO interface reveals it to be an excellent catalytic site,with HER being found to be a factor of 23x more efficient at the interface than on metallic Mg.The results not only support the plausibility of the Mg/MgO interface being an effective cathode to the adjacent anodic Mg matrix during corrosion but also contribute to the understanding of the enhanced cathodic activities observed during the anodic dissolution of magnesium.
基金supported by National Natural Science Foundation of China(52373309).
文摘Since topological quantum materials may possess interesting properties and promote the application of electronic devices,the search for new topological quantum materials has become the focus and frontier of condensed matter physics.Currently,it has been found that there are two interesting systems in topological quantum materials:topological superconducting materials and topological magnetic materials.Although research on these materials has made rapid progress,a systematic review of their synthesis,properties,and applications,particularly their synthesis,is still lacking.In this paper,we emphasize the experimental preparation of two typical topological quantum materials and then briefly introduce their potential physical properties and applications.Finally,we provide insights into current and future issues in the study of topological quantum material systems.
文摘This study demonstrates that two-and three-dimensional spatially graded,truss-based polymeric-material metamaterials can be designed for beneficial impact mitigation and energy absorption capabilities.Through a combination of numerical and experimental techniques,we highlight the broad property space of periodic viscoelastic trusses,realized using 3D printing via selective laser sintering.Extending beyond periodic designs,we investigate the impact response of spatially variant viscoelastic lattices in both two and three dimensions.Our result reveal that introducing spatial variations in lattice topology allows for redirecting of the impact trajectory,opening new opportunities for engineering and tailoring lightweight materials with target impact functionality.This is achieved through the combined selection of base material and metamaterial design.
基金supported by the National Research Foundation of Korea(NRF)grants funded by the Korean government(MSIT)(No.2020R1C1C1004434 and No.RS-202400398068)Incheon National University Research Grant in 2022(2022-0120)。
文摘This study investigates the influence of CaO(0.5,1(wt.%))alloying on the microstructural evolution,texture development and deformation behavior of AZ61 magnesium alloy.The uniaxial tension tests at room(RT)and cryogenic(CT,-150℃)temperature were performed to investigate the twinability and dislocation behavior and its consequent effect on flow stress,ductility and strain hardening rate.The results showed that the AZ61-1CaO exhibited superior strength/ductility synergy at RT with a yield strength(YS)of 223 MPa and a ductility of 23% as compared to AZ61(178 MPa,18.5%)and AZ61-0.5CaO(198 MPa,21%).Similar trend was witnessed for all the samples during CT deformation,where increase in the YS and decrease in ductility were observed.The Mtex tools based in-grain misorientation axis(IGMA)analysis of RT deformed samples revealed the higher activities of prismatic slip in AZ61-CaO,which led to superior ductility.Moreover,subsequent EBSD analysis of CT deformed samples showed the increased fraction of fine{10-12}tension twins and nucleation of multiple{10-12}twin variants caused by higher local stress concentration at the grain boundaries,which imposed the strengthening by twin-twin interaction.Lastly,the detailed investigations on strengthening contributors showed that the dislocation strengthening has the highest contribution towards strength in all samples.
基金supported by the Nano&Material Technology Development Program through the National Research Foundation of Korea(NRF),funded by the Ministry of Science and ICT(RS-2023-00234757).
文摘Although hydrofluoric acid(HF)surface treatment is known to enhance the joining of metals with polymers,there is limited information on its effect on the joining of AZ31 alloy and carbon-fiber-reinforced plastics(CFRPs)through laser-assisted metal and plastic direct joining(LAMP).This study uses the LAMP technique to produce AZ31-CFRP joints.The joining process involves as-received AZ31,HFpretreated AZ31,and thermally oxidized HF-pretreated AZ31 alloy sheets.Furthermore,the bonding strength of joints prepared with thermally oxidized AZ31 alloy sheets is examined to ascertain the combined effect of HF treatment and thermal oxidation on bonding strength.The microstructures,surface chemical interactions,and mechanical performances of joints are investigated under tensile shear loading.Various factors,such as bubble formation,CFRP resin decomposition,and mechanical interlocking considerably affect joint strength.Additionally,surface chemical interactions between the active species on metal parts and the polar amide along with carbonyl groups of polymer play a significant role in improving joint strength.Joints prepared with surface-pretreated AZ31 alloy sheets show significant improvements in bonding strength.
基金supported by the 2022 Shenzhen sustainable supporting funds for colleges and universities(20220810143642004)Shenzhen Basic Research Project(JCYJ20200109144608205 and JCYJ20210324120001003)+5 种基金Peking University Shenzhen Graduate School Research Startup Fund of Introducing Talent(No.1270110273)Shenzhen postdoctoral research fund project after outbound(No.2129933651)Shenzhen-Hong Kong Research and Development Fund(No.SGDX20201103095406024)City University of Hong Kong Strategic Research Grants(SRG)(Nos.7005264 and 7005505)Guangdong-Hong Kong Technology Cooperation Funding Scheme(TCFS)(No.GHP/085/18SZ)IER Foundation(IERF2020001 and IERF2019002).
文摘In the present research,the NaF assisted plasma electrolytic oxidation(PEO)is designed to fabricate the high-content ZnO nanoparti-cles doped coating on AZ31B alloy.The microstructure,phase constituents and corrosion behavior of the PEO coatings are investigated systematically.The results reveal that the introduction of NaF promotes the formation of MgF2 nanophases in the passivation layer on Mg alloy,decreasing the breakdown voltage and discharge voltage.As a result,the continuous arcing caused by high discharge voltage is alleviated.With the increasing of NaF content,the Zn content in the PEO coating is enhanced and the pore size in the coating is decreased correspondingly.Due to the high-content ZnO doping,the PEO coating protected AZ31B alloy demonstrates the better corrosion resistance.Compared with the bare AZ31B alloy,the high-content ZnO doped PEO coated sample shows an increased corrosion potential from-1.465 V to-1.008 V,a decreased corrosion current density from 3.043×10^(-5) A·cm^(-2) to 3.960×10^(-8) A·cm^(-2) and an increased charge transfer resistance from 1.213×10^(2) ohm·cm^(2) to 2.598×10^(5) ohm·cm^(2).Besides,the high-content ZnO doped PEO coated sample also has the excellent corrosion resistance in salt solution,exhibiting no obvious corrosion after more than 2000 h neutral salt spraying and 28 days’immersion testing.The improved corrosion resistance can be ascribed to the relative uniform distribution of ZnO in PEO coating which can transform to Zn(OH)2 and form a continuous protective layer along the corrosion interface.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.-RS-2024-00335976)。
文摘Electrochemical nitrate reduction(ENR)is an economical and eco-friendly method for converting industrial wastewater into valuable ammonia under atmospheric conditions.The main challenge lies in designing and developing highly durable ENR electrocatalysts.This study introduces defect-rich mesoporous CuO_(x) nanowires electrocatalyst synthesized using a novel solution-flame(sol-flame)hybrid method to control mesoporosity and introduce surface defects,thereby enhancing the electrochemical nitrate-toammonia production performance.We found surface defects(oxygen vacancies and Cu^(+))and unique mesoporous nanowire structure composed of tightly interconnected nanoparticles.The sol-flamesynthesized CuO_(x) nanowires(sf-CuO NWs)achieved superior ammonia yield rate(0.51 mmol h^(-1)cm^(-2)),faradaic efficiency(97.3%),and selectivity(86.2%)in 1 M KOH electrolyte(2000 ppm nitrate).This performance surpasses that of non-porous and less-defective CuO NWs and is attributed to the increased surface area and rapid electron transport facilitated by the distinctive morphology and generated defects.Theoretical calculation further suggests oxygen vacancies enhance NO_(3)^(-)adsorption on the sf-CuO NWs’surface and mitigate the competing hydrogen evolution reaction.This study outlines a strategic design and simple synthesis approach for nanowire electrocatalysts that boost the efficiency of electrochemical nitrate-to-ammonia conversion.
文摘Immersion of scaffolds in Simulated Body Fluid(10SBF)is a standardized method for evaluating their bioactivity,simulating in vivo conditions where apatite deposits can be formed on the surface of scaffold,facilitating bone integration and ensuring their suitability for bone implant purposes,ultimately contributing to long-term implant success.The effect of apatite deposition on bioactivity and cell behavior of TiO_(2)scaffolds was studied.Scaffolds were soaked in 10SBF for different durations to form HAP layer on their surface.The results proved the development of a hydroxyapatite film resembling the mineral composition of bone Extracellular Matrix(ECM)on the TiO_(2)scaffolds.The XRD test findings showed the presence of hydroxyapatite layer similar to bone at the depth of 10 nm.A decrease in the specific surface area(18.913 m^(2)g^(−1)),the total pore volume(0.045172 cm^(3)g^(−1)(at p/p0=0.990)),and the mean pore diameter(9.5537 nm),were observed by BET analysis which confirmed the formation of the apatite layer.It was found that titania scaffolds with HAP coating promoted human osteosarcoma bone cell(MG63)cell attachment and growth.It seems that immersing the scaffolds in 10SBF to form HAP coating before utilizing them for bone tissue engineering applications might be a good strategy to promote bioactivity,cell attachment,and implant fixation.
基金supported by the National Natural Science Foundation of China(Nos.52231001,51971167,and 52031011)the Xi’an Science and Technology Plan(No.2017xasjl014)+4 种基金B.G.gratefully acknowledges the financial support of the project from the Ministry of Science and Technology of China(No.2017YFA0700703)the support by the National Natural Science Foundation of China(No.92060102)E.M.and J.D.acknowledge the support at CAID by XJTU.J.D.acknowledges support from the National Natural Science Foundation of China(No.12004294)the HPC platform of Xi’an Jiaotong Universitysupported by the Office of Science,Office of Basic Energy Sciences,Materials Sciences and Engineering Division,of the U.S.Department of Energy under Contract No.DE-AC02-05-CH11231.
文摘Single-phase face-centered cubic(fcc)high/medium-entropy alloys(H/MEAs)exhibit a much higher tendency to form nanoscale deformation twins than conventional fcc metals with similar low stacking fault energies(SFEs).This extraordinary propensity for nanotwin formation in H/MEAs cannot therefore be ex-plained by their low SFEs alone.Here,using in situ compression tests of CrCoNi in comparison with Ag nanopillars inside a transmission electron microscope,we found that in the CrCoNi MEA,a high density of nanoscale twins continuously formed with an average thickness of 4.6 nm.In contrast,for similar experiments on Ag with almost identical SFE,following the nucleation of a few twins,they could further thicken to above one hundred nanometers by twin boundary migration.Molecular dynamics calculations indicated that in the highly-concentrated CrCoNi solid solution,the magnitude of the energy barriers for nucleating a stacking fault as a twin precursor in the pristine lattice and for the thickening of an existing twin both span a wide range and largely overlap with each other.Therefore,twin thickening through successive addition of atomic layers is prone to discontinuation,giving way to the nucleation of new twins at other sites where a lower energy barrier is encountered for partial-dislocation mediated fault formation.
基金Shenzhen-Hong Kong Research and Development Fund(No.SGDX20201103095406024)2022 Shenzhen Sustainable Supporting Funds for Colleges and Universities(No.20220810143642004)+9 种基金Shenzhen Basic Research Project(Nos.JCYJ20200109144608205 and JCYJ20210324120001003)Guangdong Basic and Applied Basic Research Foundation(Nos.2020A1515011301 and 2021A1515012246)Peking University Shenzhen Graduate School Research Start-up Fund of Introducing Talent(No.1270110273)Shenzhen Postdoctoral Research Fund Project after Outbound(No.2129933651)China Postdoctoral Science Foundation(No.2023M730032)City University of Hong Kong Strategic Research Grants(SRG)(7005505)City University of Hong Kong Donation Research Grants(No.9220061 and DON-RMG No.9229021)Guangdong-Hong Kong Technology Cooperation Funding Scheme(TCFS)(No.GHP/085/18SZ)Shenzhen-Hong Kong Technology Cooperation Funding Scheme(TCFS)(No.GHP/149/20SZ and CityU 9440296)IER Foundation(Nos.IERF2020001 and IERF202102).
文摘As implanted bone fixation materials,magnesium(Mg)alloys have significant advantages because the density and elastic modulus are closest to those of the human bone and they can bio-degrade in the physiological environment.However,Mg alloys degrade too rapidly and uncontrollably thus hampering clinical adoption.In this study,a highly corrosion-resistant zinc-phosphate-doped micro-arc oxidation(MAO)coating is prepared on the AZ31B alloy,and the degradation process is assessed in vitro.With increasing zinc phosphate concentrations,both the corrosion potentials and charge transfer resistance of the AZ31B alloy coated with MAO coatings increase gradually,while the corrosion current densities di-minish gradually.Immersion tests in the simulated body fluid(SBF)reveal that the increased zinc phos-phate concentration in MAO coating decreases the degradation rate,consequently reducing the release rates of Mg^(2+)and OH-in the physiological micro-environment,which obtains the lowest weight loss of only 5.22%after immersion for 56 days.Effective regulation of degradation provides a weak alkaline environment that is suitable for long-term cell growth and subsequent promotion of bone proliferation,differentiation,mineralization,and cytocompatibility.In addition,the zinc-phosphate-doped MAO coat-ings show an improved wear resistance as manifested by a wear rate of only 3.81 x 10^(-5) mm^(3) N^(-1) m^(-1).The results reveal a suitable strategy to improve the properties of biodegradable Mg alloys to balance tissue healing with mechanical degradation.
基金supported by the National Key R&D Program of China(No.2021YFE0100600)the National Natural Science Foundation of China(Nos.92166103,U23A20621,and 92066202)+1 种基金the Top-Notch Young Talents Program of Hubei.Yasir is grateful for financial support from the Pakistan Science Foundation(Project Reference:PSF/CRP-18th Protocol(05))the State Key Laboratory of Materials Processing and Die&Mould Technology(Project Reference:2021-008).
文摘Achieving a delicate synergy between mechanical robustness and antifouling attributes in coatings remains a formidable challenge for marine applications. Inspired by the assembly of nacre, we present a novel approach to fabricate a nacre-like metallic coating. This coating comprises an amorphous matrix with excellent anti-corrosion and anti-wear properties, as well as Cu-rich 3D interconnected channels for antifouling function. The coating is produced by high velocity oxygen fuel (HVOF) thermal spraying of surface-modified Fe-based amorphous powders with a Cu-layer. The resulting coating exhibits exceptional mechanical robustness, including high resistance to erosion, abrasion, and impact, surpassing conventional polymer antifouling coatings. Furthermore, the controlled Cu+ leaching capability of the in-situ constructed 3D interconnected diffusion channels, facilitated by the Cu-rich intersplats, contributes to the remarkable antifouling performance. This includes nearly 100 % resistance to bacterial adhesion after 1 day of immersion and over 98 % resistance to algal attachment after 7 d of immersion, resulting in a prolonged service lifetime. Notably, even after 200 cycles of wear damage, the Cu-modified amorphous coating still maintains its excellent antifouling properties. The Cu-rich intersplats play a critical role in transporting and sustainably leaching Cu ions, thereby accounting for the outstanding antifouling performance. Ultimately, we aim to advance the design of high-performance coatings suited for diverse marine applications, where both the mechanical robustness and antifouling properties are essential.
基金financially supported by the National Natural Science Foundation of China(Nos.52204331 and 52374315)the Major Industrial Innovation Plan of the Anhui Provincial Development and Reform Commission,China(No.AHZDCYCX-LSDT2023-01).
文摘With the gradual reduction in high-quality iron ore resources,the global steel industry faces long-term challenges.For example,the continuous increase in the Al_(2)O_(3) content of iron ore has led to a decrease in the metallurgical performance of sinter and fluctuations in slag properties.Considering calcium ferrite(CF)and composite CF(silico-ferrite of calcium and aluminum,SFCA)play a crucial role as a binding phase in high-alkalinity sinter and exhibit excellent physical strength and metallurgical performance,we propose incorporating excess Al_(2)O_(3) into SFCA to form a new binding phase with excellent properties for high-quality sinter preparation.In the synthesis of high-Al_(2)O_(3) SFCA,two high-Al_(2)O_(3) phases were identified as types A(Al_(1.2)Ca_(2.8)Fe_(8.7)O_(2)0Si_(0.8))and B(Ca_(4)Al_(4.18)Fe_(1.82)Si_(6)O_(26)).Results show that type A SFCA sample had a higher cell density(4.13 g/cm^(3))and longer Fe-O bond length(2.2193Å)than type B(3.46 g/cm^(3) and 1.9415Å),with a significantly greater lattice oxygen concentration(7.86%vs.1.85%),which demonstrates advantages in strength and reducibility.Type A SFCA sample contained a lower proportion of silicates,was predominantly composed of SFCA,and exhibited minimal porosity.Melting point and viscosity simulation tests indicate that type A SFCA sample formed a liquid phase at 880°C with a viscosity range of 0-0.35 Pa·s,which is notably lower than that of type B SFCA sample(1220°C and 0-20 Pa·s).This finding suggests that type A SFCA sample has a low initial melting temperature and viscosity,which facilitates increasing liquid-phase generation and improving flow properties.Such a condition enhances the adhesion to surrounding ore particles.Compressive strength tests reveal that type A SFCA sample(36.83-42.48 MPa)considerably outperformed type B SFCA sample(5.98-12.79 MPa)and traditional sinter(5.02-13.68 MPa).In addition,at 900°C,type A SFCA sample achieved a final reducibility of 0.89,which surpassed that of type B SFCA sample(0.83).In summary,type A SFCA sample demonstrates superior structural,thermophysical,and metallurgical properties,which highlights its promising potential for industrial applications.
基金supported by the U.S.National Science Foundation(NSF)under The Faculty Early Career Development(CAREER)Program(Grant#2046060).
文摘Artificial Intelligence(AI)has revolutionized technological development globally,delivering relatively more accurate and reliable solutions to critical challenges across various research domains.This impact is particularly notable within the field of materials science and engineering,where artificial intelligence has catalyzed the discovery of new materials,enhanced design simulations,influenced process controls,and facilitated operational analysis and predictions of material properties and behaviors.Consequently,these advancements have stream-lined the synthesis,simulation,and processing procedures,leading to material optimization for diverse appli-cations.A key area of interest within materials science is the development of hydrogen-based electrochemical systems,such as fuel cells and electrolyzers,as clean energy solutions,known for their promising high energy density and zero-emission operations.While artificial intelligence shows great potential in studying both fuel cells and electrolyzers,existing literature often separates them,with a clear gap in comprehensive studies on electrolyzers despite their similarities.This review aims to bridge that gap by providing an integrated overview of artificial intelligence’s role in both technologies.This review begins by explaining the fundamental concepts of artificial intelligence and introducing commonly used artificial intelligence-based algorithms in a simplified and clearly comprehensible way,establishing a foundational knowledge base for further discussion.Subsequently,it explores the role of artificial intelligence in materials science,highlighting the critical applications and drawing on examples from recent literature to build on the discussion.The paper then examines how artificial intelligence has propelled significant advancements in studying various types of fuel cells and electrolyzers,specifically emphasizing proton exchange membrane(PEM)based systems.It thoroughly explores the artificial intelligence tools and techniques for characterizing,manufacturing,testing,analyzing,and optimizing these systems.Additionally,the review critically evaluates the current research landscape,pinpointing progress and prevailing challenges.Through this thorough analysis,the review underscores the fundamental role of artificial intelligence in advancing the generation and utilization of clean energy,illustrating its transformative potential in this area of research.
