The current artificial bone is unable to accurately replicate the inhomogeneity and anisotropy of human cancellous bone.To address this issue,we proposed a personalized approach based on clinical CT images to design m...The current artificial bone is unable to accurately replicate the inhomogeneity and anisotropy of human cancellous bone.To address this issue,we proposed a personalized approach based on clinical CT images to design mechanical equivalent porous structures for artificial femoral heads.Firstly,supported by Micro and clinical CT scans of 21 bone specimens,the anisotropic mechanical parameters of human cancellous bone in the femoral head were characterized using clinical CT values(Hounsfield unit).After that,the equivalent porous structure of cancellous bone was designed based on the gyroid surface,the influence of its degree of anisotropy and volume fraction on the macroscopic mechanical parameters was investigated by finite element analysis.Furthermore,a mapping relationship between CT values and the porous structure was established by jointly solving the mechanical parameters of the porous structure and human cancellous bone,allowing the design of personalized gradient porous structures based on clinical CT images.Finally,to verify the mechanical equivalence,implant press-in tests were conducted on 3D-printed artificial femoral heads and human femoral heads,the influence of the porous structure’s cell size in bone-implant interaction problems was also explored.Results showed that the minimum deviations of press-in stiffness(<15%)and peak load(<5%)both occurred when the cell size was 20%to 30%of the implant diameter.In conclusion,the designed porous structure can replicate the human cancellous bone-implant interaction at a high level,indicating its effectiveness in optimizing the mechanical performance of 3D-printed artificial femoral head.展开更多
With the impact of energy crisis and environmental problems,it is urgent to develop green sustainable energy.Osmotic energy stored in the salinity difference between seawater and river water is one of the sustainable,...With the impact of energy crisis and environmental problems,it is urgent to develop green sustainable energy.Osmotic energy stored in the salinity difference between seawater and river water is one of the sustainable,abundant,and renewable energy.However,the membranes used to capture osmotic energy by reverse electrodialysis(RED)always suffer from low ion selectivity,low stability and low power.Hydrogels with three-dimensional(3D)networks have shown great potential for ion transportation and energy conversion.In this work,based on the homogeneity and porosity characteristics of acrylamide(AM)hydrogel,as well as the remarkable stability and abundant negative charge of 3-sulfopropyl acrylate potassium salt(SPAK),a high-performance AM/SPAK cation-selective hydrogel membrane was successfully developed for harvesting osmotic energy.Compared to AM hydrogels,utilizing AM/SPAK as a monomer mixture greatly facilitated the preparation of homogeneous polymers,exhibiting a porous structure,exceptional ion selectivity,and remarkable stability.A maximum output power density of 13.73 W/m^(2)was achieved at a 50-fold NaCl concentration gradient,exceeding the commercial requirement of 5 W/m^(2).This work broadens the idea for the construction and application of composite hydrogel in high efficiency osmotic energy conversion.展开更多
Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium...Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium-deficient hydroxyapatite(CDHA)scaffolds with three-level hierarchical porous structure were fabricated by indirect 3D printing technology and particulate leaching method.The sacrificial template scaffolds were fabricated using a photo-curing 3D printer,which provided a prerequisite for the integral structure and interconnected macropores of CDHA scaffolds.Additionally,20 wt%pore former was incorporated into the slurry to enhance the content of smaller pores within the CDHA-2 scaffolds,and then the CDHA-2 scaffolds were sintered to remove the sacrificial template scaffolds and pore former.The obtained CDHA-2 scaffolds exhibited interconnected macropores(300-400μm),minor pores(∼10-100μm),and micropores(<10μm)distributed throughout the scaffolds,which could promote bone tissue ingrowth,increase surface roughness,and enhance protein adsorption of scaffolds.In vitro studies identified that CDHA-2 scaffolds had nanocrystal grains,high specific surface area,and outstanding protein adsorption capacity,which could provide a microenvironment for cell adhesion,spreading,and proliferation.In addition,the murine intramuscular implantation experiment suggested that CDHA-2 scaffolds exhibited excellent osteoinductivity and were superior to traditional BCP ceramics under conditions without the addition of live cells and exogenous growth factors.The rabbit calvarial defect repair results indicated that CDHA-2 scaffolds could enhance in situ bone regeneration.In conclusion,these findings demonstrated that the hierarchical porous structure of CDHA scaffolds was a pivotal factor in modulating osteoinductivity and bone regeneration,and CDHA-2 scaffolds were potential candidates for bone regeneration.展开更多
Faced with complex operational environments,liquid metal divertors are considered alternative solutions to traditional solid divertors.Experiments have been conducted using a self-designed embedded multichannel capill...Faced with complex operational environments,liquid metal divertors are considered alternative solutions to traditional solid divertors.Experiments have been conducted using a self-designed embedded multichannel capillary porous structure(EM-CPS)for plasma irradiation of lithium(Li)-prefilled EM-CPS in the high-density linear plasma device(SCU-PSI).The optical image analysis of the interaction region between the plasma and Li vapor shows that the region is not a regular geometric shape and the point of strongest light emission appears 1–2 cm in front of the target rather than on its surface.The irregularity is due to the uneven distribution and density of the Li vapor,as well as the radial and axial attenuation of the plasma.As the plasma discharge parameters increase,the vapor profile initially expands globally and then contracts locally,with the point of the strongest light emission gradually moving towards the target surface.The spectral lines of Li 670.78 nm and Ar 763.51 nm in the interaction region are produced by deexcitation.These lines gradually decrease in intensity along the axial direction,which is close to the trend of light emission intensity that initially increases and then decreases along the same direction.These findings provide a reference for studying the interaction mechanism between plasma and liquid Li capillary porous structures in linear plasma devices and future tokamak.展开更多
Flexible piezoresistive sensors based on biomimetic microstructures are prospective for broad application in motion monitoring.However,the design and preparation processes of most biomimetic microstructures in the exi...Flexible piezoresistive sensors based on biomimetic microstructures are prospective for broad application in motion monitoring.However,the design and preparation processes of most biomimetic microstructures in the existing studies are complicated,and there are few studies on pore size control.Herein,the porous structure of human bones was used as a biomimetic prototype,and optimally designed by creating a theoretical equivalent sensor model and a finite element model.Soluble raw materials such as sugar and salt in different particle sizes were pressed into porous templates.Based on the template method,porous structures in different pore sizes were prepared using polydimethylsiloxane(PDMS)polymer as the substrate.On this basis,graphene oxide conductive coating was prepared with the modified Hummers method and then deposited via dip coating onto the substrate.Finally,a PDMS-based porous structure biomimetic flexible piezoresistive sensor was developed.Mechanically,the deformation of the sensor under the same load increased with the pore size rising from 0.3 to 1.5 mm.Electrically,the resistance rang of the sensor was enlarged as the pore size rose.The resistance variation rates of samples with pore sizes of 0.3,1.0,and 1.5 mm at approximately the 200th cycle were 63%,79%,and 81%,respectively;at the 500th cycle,these values were 63%,77%,and 79%;and at the 1000th cycle,they stabilized at 63%,74%,and 76%.These results indicate that the fabricated sensor exhibits high stability and fatigue resistance.At the pressure of 0–25 kPa,the sensitivity rose from 0.0688 to 0.1260 kPa−1,and the performance was enhanced by 83%.After 1,000 cycles of compression testing,the signal output was stable,and no damage was caused to the substrate.Further application tests showed the biomimetic sensor accurately and effectively identified human joint motions and gestures,and has potential application value in human motion monitoring.展开更多
The development of sustainable electrode materials for energy storage systems has become very important and porous carbons derived from biomass have become an important candidate because of their tunable pore structur...The development of sustainable electrode materials for energy storage systems has become very important and porous carbons derived from biomass have become an important candidate because of their tunable pore structure,environmental friendliness,and cost-effectiveness.Recent advances in controlling the pore structure of these carbons and its relationship between to is energy storage performance are discussed,emphasizing the critical role of a balanced distribution of micropores,mesopores and macropores in determining electrochemical behavior.Particular attention is given to how the intrinsic components of biomass precursors(lignin,cellulose,and hemicellulose)influence pore formation during carbonization.Carbonization and activation strategies to precisely control the pore structure are introduced.Finally,key challenges in the industrial production of these carbons are outlined,and future research directions are proposed.These include the establishment of a database of biomass intrinsic structures and machine learning-assisted pore structure engineering,aimed at providing guidance for the design of high-performance carbon materials for next-generation energy storage devices.展开更多
Four types of Mg-5Zn porous scaffolds with different pore geometries,including body-centered cubic(bcc),the rhombic dodecahedron(RD),gyroid(G),and primitive(P)types,were designed and fabricated using selective laser m...Four types of Mg-5Zn porous scaffolds with different pore geometries,including body-centered cubic(bcc),the rhombic dodecahedron(RD),gyroid(G),and primitive(P)types,were designed and fabricated using selective laser melting.Their forming quality,compression mechanical properties,and degradation behavior were investigated.Results indicate that the fabricated scaffolds exhibit good dimensional accuracy,and the surface chemical polishing treatment significantly improves the forming quality and reduces porosity error in porous scaffolds.Compared to the ones with rod structures(bcc,RD),the scaffolds with surface structures(G,P)have less powder particle adhesion.The G porous scaffold exhibits the best forming quality for the same design porosity.The predominant failure mode of scaffolds during compression is a 45°shear fracture.At a porosity of 75%,the compression property of all scaffolds meets the compressive property requirements of cancellous bone,while bcc and G structures show relatively better compression property.After immersion in Hank's solution for 168 h,the B-2-75% pore structure scaffold exhibits severe localized corrosion,with fractures in partial pillar connections.In contrast,the G-3-75% pore structure scaffold mainly undergoes uniform corrosion,maintaining structural integrity,and its corrosion rate and loss of compressive properties are less than those of the B-2-75%structure.After comparison,the G-pore structure scaffold is preferred.展开更多
The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-...The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-heterostructured nanoporous CoFe/CoFe_(2)O_(4) and CeO_(2−x),in situ grown on nickel foam(NF),holds great promise as a high-efficient bifunctional electrocatalyst(named R-CoFe/Ce/NF)for water splitting.Experimental characterization verifies surface reconstruction from CoFe alloy/oxide to highly active CoFeOOH during in situ electrochemical polarization.By virtues of three-dimensional nanoporous architecture and abundant electroactive CoFeOOH/CeO_(2−x) heterostructure interfaces,the R-CoFe/Ce/NF electrode achieves low overpotentials for oxygen evolution(η_(10)=227 mV;η_(500)=450 mV)and hydrogen evolution(η_(10)=35 mV;η_(408)=560 mV)reactions with high normalized electrochemical active surface areas,respectively.Additionally,the alkaline full water splitting electrolyzer of R-CoFe/Ce/NF||R-CoFe/Ce/NF achieves a current density of 50 mA·cm^(−2) only at 1.75 V;the decline of activity is satisfactory after 100-h durability test at 300 mA·cm^(−2).Density functional theory also demonstrates that the electron can transfer from CeO_(2−x) by virtue of O atom to CoFeOOH at CoFeOOH/CeO_(2−x) heterointerfaces and enhancing the adsorption of reactant,thus optimizing electronic structure and Gibbs free energies for the improvement of the activity for water splitting.展开更多
Thick electrode,with its feasibility and cost-effectiveness in lithium-ion batteries(LIBs),has attracted significant attention as a promising approach maximizing the energy density of battery.Through raising the mass ...Thick electrode,with its feasibility and cost-effectiveness in lithium-ion batteries(LIBs),has attracted significant attention as a promising approach maximizing the energy density of battery.Through raising the mass loading of active materials without altering the fundamental chemical attributes,thick electrodes can boost the energy density of the batteries effectively.Nevertheless,as the thickness of the electrode increases,the ionic conductivity of the electrode decreases,leading to abominable polarization in the thickness direction,which severely hampers the practical application of a thick electrode.This work proposes a novel porous gradient design of high-performance thick electrodes for LIBs.By constructing a porous structure that serves as a fast transport pathway for lithium(Li)ions,the ion transport kinetics within thick electrodes are significantly enhanced.Meanwhile,a particle size gradient design is incorporated to further mitigate polarization effects within the electrode,leading to substantial improvements in reaction homogeneity and material utilization.Employing this strategy,we have fabricated a porous gradient nanocellulose-carbon-nanotube based thick electrode,which exhibits an impressive capacity retention of 86.7%at a high mass loading of LiCoO_(2)(LCO)active material(20 mg cm^(-2))and a high current density of 5mA cm^(-2).展开更多
This work examines the impact of incorporating the physiological conditions of human cancellous bone,by integrating similar porosity of porous Fe with the cancellous bone under dynamic immersion test.All of the porous...This work examines the impact of incorporating the physiological conditions of human cancellous bone,by integrating similar porosity of porous Fe with the cancellous bone under dynamic immersion test.All of the porous Fe specimens with~80%porosity were immersed in Simulated Body Fluid(SBF)with a flow rate of 0.3 ml/min integrated with cancellous bone for 7,14 and 28 days.Porous Fe with the lowest surface area has the highest degradation rate despite having the lowest relative weight loss.The relationship between fluid induced shear stress and weight loss of specimens have been established.展开更多
Ceramic spheres,typically with a particle diameter of less than 0.8 mm,are frequently utilized as a critical proppant material in hydraulic fracturing for petroleum and natural gas extraction.Porous ceramic spheres wi...Ceramic spheres,typically with a particle diameter of less than 0.8 mm,are frequently utilized as a critical proppant material in hydraulic fracturing for petroleum and natural gas extraction.Porous ceramic spheres with artificial inherent pores are an important type of lightweight proppant,enabling their transport to distant fracture extremities and enhancing fracture conductivity.However,the focus frequently gravitates towards the low-density advantage,often overlooking the pore geometry impacts on compressive strength by traditional strength evaluation.This paper numerically bypasses such limitations by using a combined finite and discrete element method(FDEM)considering experimental results.The mesh size of the model undergoes validation,followed by the calibration of cohesive element parameters via the single particle compression test.The stimulation elucidates that proppants with a smaller pore size(40μm)manifest crack propagation evolution at a more rapid pace in comparison to their larger-pore counterparts,though the influence of pore diameter on overall strength is subtle.The inception of pores not only alters the trajectory of crack progression but also,with an increase in porosity,leads to a discernible decline in proppant compressive strength.Intriguingly,upon crossing a porosity threshold of 10%,the decrement in strength becomes more gradual.A denser congregation of pores accelerates crack propagation,undermining proppant robustness,suggesting that under analogous conditions,hollow proppants might not match the strength of their porous counterparts.This exploration elucidates the underlying mechanisms of proppant failure from a microstructural perspective,furnishing pivotal insights that may guide future refinements in the architectural design of porous proppant.展开更多
As a catalyst of the air cathode in zinc-air batteries,tungstic acid ferrous(FeWO_(4)),a nanoscale transition metal tungstate,shows a broad application prospect in the oxygen reduction reaction(ORR).While FeWO_(4)poss...As a catalyst of the air cathode in zinc-air batteries,tungstic acid ferrous(FeWO_(4)),a nanoscale transition metal tungstate,shows a broad application prospect in the oxygen reduction reaction(ORR).While FeWO_(4)possesses favorable electrochemical properties and thermodynamic stability,its intrinsic semiconductor characteristics result in a relatively slow electron transfer rate,limiting the ORR catalytic activity.In this work,the electronic structure of FeWO_(4)is significantly modulated by introducing phosphorus(P)atoms with abundant valence electrons.The P doping can adjust the electronic structure of FeWO_(4)and then optimize oxygen-containing intermediates'absorption/desorption efficiency to achieve improved ORR activity.Furthermore,the sodium chloride template is utilized to construct a porous carbon framework for anchoring phosphorus-doped iron tungstate(P-FeWO_(4)/PNC).The porous carbon skeleton provides numerous active sites for the absorption/desorption and redox reactions on the P-FeWO_(4)/PNC surface and serves as mass transport channels for reactants and intermediates.The P-FeWO_(4)/PNC demonstrates ORR performance(E1/2=0.86 V vs.RHE).Furthermore,the zinc-air batteries incorporating the P-FeWO_(4)/PNC composite demonstrate an increased peak power density(172.2 mW·cm^(-2)),high specific capacity(810.1 mAh·g^(-1)),and sustained long-term cycling stability lasting up to 240 h.This research not only contributes to the advancement of cost-effective tungsten-based non-precious metallic ORR catalysts,but also guides their utilization in zinc-air batteries.展开更多
Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycl...Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycling stability and reaction kinetics.To address these challenges,we designed a core–shell heterostructure(VONC-T,T represents temperature)composed of a VN core and a porous carbon shell.This structure was synthesized via in-situ construction,involving optimized ratio of coating a zinc-based zeolitic imidazolate framework(ZIF-8)onto a vanadium-based metal-organic framework(MIL-47(V)),followed by a thermal treatment.This process ensures a high degree of interfacial stability between the core and shell,effectively mitigating the structural variation of VN during irreversible phase transitions and enhancing the overall structural stability.During thermal driving,the volatilization of zinc within the shell layer created a porous channel effect,which facilitating Zn^(2+)diffusion.The enhancement of Zn²⁺diffusion strengthens the efficient conversion of VN to amorphous VOx,labeled as VONC-T-a,which provides more active sites and consequently results in a high specific capacity.The optimized heterostructure of VONC-900-a presented high reversible capacity of 387.2 mAh g^(−1)at 0.2 A g^(−1)and demonstrated excellent rate performance,achieving 274.5 mAh g^(−1)at 20 A g^(−1),while maintaining a capacity retention rate of 93.3%after 5000 cycles at 10 A g^(−1).Density functional theory calculations confirmed improved reaction kinetics in the core–shell structure.This study not only highlights the potential of amorphous vanadium oxide core–shell heterostructure for AZIBs but also provides new insights into the conversion mechanisms of VN.展开更多
The bioinert nature of polyether ether ketone(PEEK)material limits the widespread clinical application of PEEK implants.Although the porous structure is considered to improve osseointegration of PEEK implants,it is ha...The bioinert nature of polyether ether ketone(PEEK)material limits the widespread clinical application of PEEK implants.Although the porous structure is considered to improve osseointegration of PEEK implants,it is hardly used due to its mechanical properties.This study investigated the combined influence of the porous structure and in vivo mechanical stimulation on implantation safety and bone growth based on finite element analysis of the biomechanical behavior of the implantation system.The combined control of pore size and screw preloads allows the porous PEEK implant to achieve good osseointegration while maintaining a relatively high safety level.A pore size of 600μm and a preload of 0.05 N·m are the optimal combination for the long-term stability of the implant,with which the safety factor of the implant is>2,and the predicted percentage of effective bone growth area of the bone-implant interface reaches 97%.For further clinical application,PEEK implants were fabricated with fused filament fabrication(FFF)three-dimensional(3D)printing,and clinical outcomes demonstrated better bone repair efficacy and long-term stability of porous PEEK implants compared to solid PEEK implants.Moreover,good osteointegration performance of 3D-printed porous PEEK implants was observed,with an average bone volume fraction>40%three months after implantation.In conclusion,3D-printed porous PEEK implants have great potential for clinical application,with validated implantation safety and good osseointegration.展开更多
Because of tempting magnetic-dielectric synergies and interfacial effects,designing a simple and low-cost route for producing multidimensional carbon-based magnetic nanocomposites is very important for the development...Because of tempting magnetic-dielectric synergies and interfacial effects,designing a simple and low-cost route for producing multidimensional carbon-based magnetic nanocomposites is very important for the development of microwave absorbers(MAs).In this paper,a facile and propagable Ni-nitrilotriacetic acid chelate(NAC)derived strategy was proposed to selectively fabricate zero-dimensional(0D)/one-dimensional(1D)porous Ni/C magnetic heterostructured nanorods(MHNRs)consisting of 1D carbon nanorod,lots of pores and 0D Ni nanoparticles via a combined hydrothermal and thermally treated methods.The porous Ni/C MHNRs displayed the progressively improved Ni and C crystallinity by controlling the temperature,which resulted in the tunable electromagnetic and microwave absorption properties(MAPs).Additionally,0D/1D porous CoNi/C and Co/C MHNRs could be selectively produced through this strategy by adopting CoNi-NAC and Co-NAC as precursors.Benefiting from desirable interface and magnetic/dielectric synergies,the acquired 0D/1D porous Ni/C,CoNi/C and Co/C MHNRs presented excellent MAPs and certain corrosion resistance properties.In especial,Co/C MHNRs displayed a strong absorption capacity(−47.89 dB),an ultrawide effective absorption bandwidth(8.40 GHz)and small matching thicknesses(∼2 mm),which were a desirable candidate for MAs.Consequently,a facile,low-cost and propagable metal-NAC derived strategy was proposed to synthesize 0D/1D porous carbon-based MHNRs,which presented an alternative technique to develop lightweight efficient MAs.展开更多
Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via lo...Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via low-temperature coprecipitation,exhibiting excellent performance for the selective hydrogenation of 5-hydroxymethylfurfural(HMF).A linear correlation is first observed between solvent polarity(E_(T)(30))and product selectivity within both polar aprotic and protic solvent classes,suggesting that solvent properties play a vital role in directing reaction pathways.Among these,1,4-dioxane(aprotic)favors the formation of 2,5-bis(hydroxymethyl)furan(BHMF)with 97.5%selectivity,while isopropanol(iPrOH,protic)promotes 2,5-dimethylfuran production with up to 99.5%selectivity.Mechanistic investigations further reveal that beyond polarity,proton-donating ability is critical in facilitating hydrodeoxygenation.iPrOH enables a hydrogen shuttle mechanism where protons assist in hydroxyl group removal,lowering the activation barrier.In contrast,1,4-dioxane,lacking hydrogen bond donors,stabilizes BHMF and hinders further conversion.Density functional theory calculations confirm a lower activation energy in iPrOH(0.60 eV)compared to 1,4-dioxane(1.07 eV).This work offers mechanistic insights and a practical strategy for solvent-mediated control of product selectivity in biomass hydrogenation,highlighting the decisive role of solvent-catalyst-substrate interactions.展开更多
Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is p...Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is proposed.The electric field applied between the template and the substrate drives the contact,tilting,filling,and holding processes.By accurately controlling the introduced included angle between the flexible template and the substrate,tilted nanostructures with a controllable angle are imprinted onto the substrate,although they are vertical on the template.By flexibly adjusting the electric field intensity and the included angle,large-area uniform-tilted,gradient-tilted,and high-angle-tilted nanostructures are fabricated.In contrast to traditional replication,the morphology of the nanoimprinting structure is extended to customized control.This work provides a cost-effective,efficient,and versatile technology for the fabrication of various large-area tilted metasurface structures.As an illustration,a tilted nanograting with a high coupling efficiency is fabricated and integrated into augmented reality displays,demonstrating superior imaging quality.展开更多
Vacancy defects,as fundamental disruptions in metallic lattices,play an important role in shaping the mechanical and electronic properties of aluminum crystals.However,the influence of vacancy position under coupled t...Vacancy defects,as fundamental disruptions in metallic lattices,play an important role in shaping the mechanical and electronic properties of aluminum crystals.However,the influence of vacancy position under coupled thermomechanical fields remains insufficiently understood.In this study,transmission and scanning electron microscopy were employed to observe dislocation structures and grain boundary heterogeneities in processed aluminum alloys,suggesting stress concentrations and microstructural inhomogeneities associated with vacancy accumulation.To complement these observations,first-principles calculations and molecular dynamics simulations were conducted for seven single-vacancy configurations in face-centered cubic aluminum.The stress response,total energy,density of states(DOS),and differential charge density were examined under varying compressive strain(ε=0–0.1)and temperature(0–600 K).The results indicate that face-centered vacancies tend to reduce mechanical strength and perturb electronic states near the Fermi level,whereas corner and edge vacancies appear to have weaker effects.Elevated temperatures may partially restore electronic uniformity through thermal excitation.Overall,these findings suggest that vacancy position exerts a critical but position-dependent influence on coupled structure-property relationships,offering theoretical insights and preliminary experimental support for defect-engineered aluminum alloy design.展开更多
A solid-phase sintering process for the low-cost fabrication of composite micro-channels was developed. Three kinds of composite micro-channels with metallic porous structures were designed. The sintering process was ...A solid-phase sintering process for the low-cost fabrication of composite micro-channels was developed. Three kinds of composite micro-channels with metallic porous structures were designed. The sintering process was studied and optimized to obtain porous-structured micro-channels with high porosity. The flow resistance and heat transfer performance in the composite micro-channels were investigated. The composite micro-channels show acceptable flow resistance, significant enhancement of heat transfer and dramatic improvement of flow boiling stability, which indicates a promising prospect for the application in forced convective heat transfer.展开更多
基金supported by the National Key R&D Program of China(Grant No.2021YFC2501700).
文摘The current artificial bone is unable to accurately replicate the inhomogeneity and anisotropy of human cancellous bone.To address this issue,we proposed a personalized approach based on clinical CT images to design mechanical equivalent porous structures for artificial femoral heads.Firstly,supported by Micro and clinical CT scans of 21 bone specimens,the anisotropic mechanical parameters of human cancellous bone in the femoral head were characterized using clinical CT values(Hounsfield unit).After that,the equivalent porous structure of cancellous bone was designed based on the gyroid surface,the influence of its degree of anisotropy and volume fraction on the macroscopic mechanical parameters was investigated by finite element analysis.Furthermore,a mapping relationship between CT values and the porous structure was established by jointly solving the mechanical parameters of the porous structure and human cancellous bone,allowing the design of personalized gradient porous structures based on clinical CT images.Finally,to verify the mechanical equivalence,implant press-in tests were conducted on 3D-printed artificial femoral heads and human femoral heads,the influence of the porous structure’s cell size in bone-implant interaction problems was also explored.Results showed that the minimum deviations of press-in stiffness(<15%)and peak load(<5%)both occurred when the cell size was 20%to 30%of the implant diameter.In conclusion,the designed porous structure can replicate the human cancellous bone-implant interaction at a high level,indicating its effectiveness in optimizing the mechanical performance of 3D-printed artificial femoral head.
基金financial support by the National Natural Science Foundation of China(No.21805017)。
文摘With the impact of energy crisis and environmental problems,it is urgent to develop green sustainable energy.Osmotic energy stored in the salinity difference between seawater and river water is one of the sustainable,abundant,and renewable energy.However,the membranes used to capture osmotic energy by reverse electrodialysis(RED)always suffer from low ion selectivity,low stability and low power.Hydrogels with three-dimensional(3D)networks have shown great potential for ion transportation and energy conversion.In this work,based on the homogeneity and porosity characteristics of acrylamide(AM)hydrogel,as well as the remarkable stability and abundant negative charge of 3-sulfopropyl acrylate potassium salt(SPAK),a high-performance AM/SPAK cation-selective hydrogel membrane was successfully developed for harvesting osmotic energy.Compared to AM hydrogels,utilizing AM/SPAK as a monomer mixture greatly facilitated the preparation of homogeneous polymers,exhibiting a porous structure,exceptional ion selectivity,and remarkable stability.A maximum output power density of 13.73 W/m^(2)was achieved at a 50-fold NaCl concentration gradient,exceeding the commercial requirement of 5 W/m^(2).This work broadens the idea for the construction and application of composite hydrogel in high efficiency osmotic energy conversion.
基金supported by the National Key Research and Development Program of China(No.2019YFA0110600)the Science and Technology Support Program of Sichuan Province(No.2019YJ0161).
文摘Hierarchical porous structure,which include macropores,minor pores,and micropores in scaffolds,are essential in the multiple biological functions of bone repair and regeneration.In this study,patientcustomized calcium-deficient hydroxyapatite(CDHA)scaffolds with three-level hierarchical porous structure were fabricated by indirect 3D printing technology and particulate leaching method.The sacrificial template scaffolds were fabricated using a photo-curing 3D printer,which provided a prerequisite for the integral structure and interconnected macropores of CDHA scaffolds.Additionally,20 wt%pore former was incorporated into the slurry to enhance the content of smaller pores within the CDHA-2 scaffolds,and then the CDHA-2 scaffolds were sintered to remove the sacrificial template scaffolds and pore former.The obtained CDHA-2 scaffolds exhibited interconnected macropores(300-400μm),minor pores(∼10-100μm),and micropores(<10μm)distributed throughout the scaffolds,which could promote bone tissue ingrowth,increase surface roughness,and enhance protein adsorption of scaffolds.In vitro studies identified that CDHA-2 scaffolds had nanocrystal grains,high specific surface area,and outstanding protein adsorption capacity,which could provide a microenvironment for cell adhesion,spreading,and proliferation.In addition,the murine intramuscular implantation experiment suggested that CDHA-2 scaffolds exhibited excellent osteoinductivity and were superior to traditional BCP ceramics under conditions without the addition of live cells and exogenous growth factors.The rabbit calvarial defect repair results indicated that CDHA-2 scaffolds could enhance in situ bone regeneration.In conclusion,these findings demonstrated that the hierarchical porous structure of CDHA scaffolds was a pivotal factor in modulating osteoinductivity and bone regeneration,and CDHA-2 scaffolds were potential candidates for bone regeneration.
基金supported by the National Key Research and Development Program of China(No.2022YFE03130000)。
文摘Faced with complex operational environments,liquid metal divertors are considered alternative solutions to traditional solid divertors.Experiments have been conducted using a self-designed embedded multichannel capillary porous structure(EM-CPS)for plasma irradiation of lithium(Li)-prefilled EM-CPS in the high-density linear plasma device(SCU-PSI).The optical image analysis of the interaction region between the plasma and Li vapor shows that the region is not a regular geometric shape and the point of strongest light emission appears 1–2 cm in front of the target rather than on its surface.The irregularity is due to the uneven distribution and density of the Li vapor,as well as the radial and axial attenuation of the plasma.As the plasma discharge parameters increase,the vapor profile initially expands globally and then contracts locally,with the point of the strongest light emission gradually moving towards the target surface.The spectral lines of Li 670.78 nm and Ar 763.51 nm in the interaction region are produced by deexcitation.These lines gradually decrease in intensity along the axial direction,which is close to the trend of light emission intensity that initially increases and then decreases along the same direction.These findings provide a reference for studying the interaction mechanism between plasma and liquid Li capillary porous structures in linear plasma devices and future tokamak.
基金supported by the National Natural Science Foundation of China(52175270)the Project of Scientifc and Technological Development Plan of Jilin Province(20220508130RC)+3 种基金the Science and Technology Development Program of Jilin Province(YDZJ202501ZYTS370)the Scientific Research Project of Education Department of Jilin Province(JJKH20251196KJ)the Scientific Research Project of Education Department of Jilin Province(JJKH20251195KJ)the Key Project of State Key Laboratory of Changchun City(23GZZ14).
文摘Flexible piezoresistive sensors based on biomimetic microstructures are prospective for broad application in motion monitoring.However,the design and preparation processes of most biomimetic microstructures in the existing studies are complicated,and there are few studies on pore size control.Herein,the porous structure of human bones was used as a biomimetic prototype,and optimally designed by creating a theoretical equivalent sensor model and a finite element model.Soluble raw materials such as sugar and salt in different particle sizes were pressed into porous templates.Based on the template method,porous structures in different pore sizes were prepared using polydimethylsiloxane(PDMS)polymer as the substrate.On this basis,graphene oxide conductive coating was prepared with the modified Hummers method and then deposited via dip coating onto the substrate.Finally,a PDMS-based porous structure biomimetic flexible piezoresistive sensor was developed.Mechanically,the deformation of the sensor under the same load increased with the pore size rising from 0.3 to 1.5 mm.Electrically,the resistance rang of the sensor was enlarged as the pore size rose.The resistance variation rates of samples with pore sizes of 0.3,1.0,and 1.5 mm at approximately the 200th cycle were 63%,79%,and 81%,respectively;at the 500th cycle,these values were 63%,77%,and 79%;and at the 1000th cycle,they stabilized at 63%,74%,and 76%.These results indicate that the fabricated sensor exhibits high stability and fatigue resistance.At the pressure of 0–25 kPa,the sensitivity rose from 0.0688 to 0.1260 kPa−1,and the performance was enhanced by 83%.After 1,000 cycles of compression testing,the signal output was stable,and no damage was caused to the substrate.Further application tests showed the biomimetic sensor accurately and effectively identified human joint motions and gestures,and has potential application value in human motion monitoring.
文摘The development of sustainable electrode materials for energy storage systems has become very important and porous carbons derived from biomass have become an important candidate because of their tunable pore structure,environmental friendliness,and cost-effectiveness.Recent advances in controlling the pore structure of these carbons and its relationship between to is energy storage performance are discussed,emphasizing the critical role of a balanced distribution of micropores,mesopores and macropores in determining electrochemical behavior.Particular attention is given to how the intrinsic components of biomass precursors(lignin,cellulose,and hemicellulose)influence pore formation during carbonization.Carbonization and activation strategies to precisely control the pore structure are introduced.Finally,key challenges in the industrial production of these carbons are outlined,and future research directions are proposed.These include the establishment of a database of biomass intrinsic structures and machine learning-assisted pore structure engineering,aimed at providing guidance for the design of high-performance carbon materials for next-generation energy storage devices.
基金Science and Technology Planning Project of Inner Mongolia Science and Technology Department(2022YFSH0021)Key Research and Development Program of Shaanxi Province(2024SF2-GJHX-14,2021SF-296)。
文摘Four types of Mg-5Zn porous scaffolds with different pore geometries,including body-centered cubic(bcc),the rhombic dodecahedron(RD),gyroid(G),and primitive(P)types,were designed and fabricated using selective laser melting.Their forming quality,compression mechanical properties,and degradation behavior were investigated.Results indicate that the fabricated scaffolds exhibit good dimensional accuracy,and the surface chemical polishing treatment significantly improves the forming quality and reduces porosity error in porous scaffolds.Compared to the ones with rod structures(bcc,RD),the scaffolds with surface structures(G,P)have less powder particle adhesion.The G porous scaffold exhibits the best forming quality for the same design porosity.The predominant failure mode of scaffolds during compression is a 45°shear fracture.At a porosity of 75%,the compression property of all scaffolds meets the compressive property requirements of cancellous bone,while bcc and G structures show relatively better compression property.After immersion in Hank's solution for 168 h,the B-2-75% pore structure scaffold exhibits severe localized corrosion,with fractures in partial pillar connections.In contrast,the G-3-75% pore structure scaffold mainly undergoes uniform corrosion,maintaining structural integrity,and its corrosion rate and loss of compressive properties are less than those of the B-2-75%structure.After comparison,the G-pore structure scaffold is preferred.
基金sponsored by the National Natural Science Foundation of China(Nos.5210125 and 52375422)the Science Research Project of Hebei Education Department(No.BJK2023058)the Natural Science Foundation of Hebei Province(Nos.E2020208069,B2020208083 and E202320801).
文摘The stability and electrocatalytic efficiency of transition metal oxides for water splitting is determined by geometric and electronic structure,especially under high current densities.Herein,a newly designed lamella-heterostructured nanoporous CoFe/CoFe_(2)O_(4) and CeO_(2−x),in situ grown on nickel foam(NF),holds great promise as a high-efficient bifunctional electrocatalyst(named R-CoFe/Ce/NF)for water splitting.Experimental characterization verifies surface reconstruction from CoFe alloy/oxide to highly active CoFeOOH during in situ electrochemical polarization.By virtues of three-dimensional nanoporous architecture and abundant electroactive CoFeOOH/CeO_(2−x) heterostructure interfaces,the R-CoFe/Ce/NF electrode achieves low overpotentials for oxygen evolution(η_(10)=227 mV;η_(500)=450 mV)and hydrogen evolution(η_(10)=35 mV;η_(408)=560 mV)reactions with high normalized electrochemical active surface areas,respectively.Additionally,the alkaline full water splitting electrolyzer of R-CoFe/Ce/NF||R-CoFe/Ce/NF achieves a current density of 50 mA·cm^(−2) only at 1.75 V;the decline of activity is satisfactory after 100-h durability test at 300 mA·cm^(−2).Density functional theory also demonstrates that the electron can transfer from CeO_(2−x) by virtue of O atom to CoFeOOH at CoFeOOH/CeO_(2−x) heterointerfaces and enhancing the adsorption of reactant,thus optimizing electronic structure and Gibbs free energies for the improvement of the activity for water splitting.
基金financially supported by the National Key R&D Program of China(2023YFB2503900)the National Natural Science Foundation of China(U22A20140,52072138)the Shenzhen Science and Technology Program(JCYJ20220818100418040,JCYJ20220530160816038)。
文摘Thick electrode,with its feasibility and cost-effectiveness in lithium-ion batteries(LIBs),has attracted significant attention as a promising approach maximizing the energy density of battery.Through raising the mass loading of active materials without altering the fundamental chemical attributes,thick electrodes can boost the energy density of the batteries effectively.Nevertheless,as the thickness of the electrode increases,the ionic conductivity of the electrode decreases,leading to abominable polarization in the thickness direction,which severely hampers the practical application of a thick electrode.This work proposes a novel porous gradient design of high-performance thick electrodes for LIBs.By constructing a porous structure that serves as a fast transport pathway for lithium(Li)ions,the ion transport kinetics within thick electrodes are significantly enhanced.Meanwhile,a particle size gradient design is incorporated to further mitigate polarization effects within the electrode,leading to substantial improvements in reaction homogeneity and material utilization.Employing this strategy,we have fabricated a porous gradient nanocellulose-carbon-nanotube based thick electrode,which exhibits an impressive capacity retention of 86.7%at a high mass loading of LiCoO_(2)(LCO)active material(20 mg cm^(-2))and a high current density of 5mA cm^(-2).
基金funded by the Ministry of Higher Education,Malaysia under the Fundamental Research Grant Scheme(FRGS/1/2018/TK03/UTM/02/8).
文摘This work examines the impact of incorporating the physiological conditions of human cancellous bone,by integrating similar porosity of porous Fe with the cancellous bone under dynamic immersion test.All of the porous Fe specimens with~80%porosity were immersed in Simulated Body Fluid(SBF)with a flow rate of 0.3 ml/min integrated with cancellous bone for 7,14 and 28 days.Porous Fe with the lowest surface area has the highest degradation rate despite having the lowest relative weight loss.The relationship between fluid induced shear stress and weight loss of specimens have been established.
基金the financial support provided by Tianfu Yongxing Laboratory Organized Research Project Funding(No.2023CXXM01)the ARC linkage program(No.LP200100420).
文摘Ceramic spheres,typically with a particle diameter of less than 0.8 mm,are frequently utilized as a critical proppant material in hydraulic fracturing for petroleum and natural gas extraction.Porous ceramic spheres with artificial inherent pores are an important type of lightweight proppant,enabling their transport to distant fracture extremities and enhancing fracture conductivity.However,the focus frequently gravitates towards the low-density advantage,often overlooking the pore geometry impacts on compressive strength by traditional strength evaluation.This paper numerically bypasses such limitations by using a combined finite and discrete element method(FDEM)considering experimental results.The mesh size of the model undergoes validation,followed by the calibration of cohesive element parameters via the single particle compression test.The stimulation elucidates that proppants with a smaller pore size(40μm)manifest crack propagation evolution at a more rapid pace in comparison to their larger-pore counterparts,though the influence of pore diameter on overall strength is subtle.The inception of pores not only alters the trajectory of crack progression but also,with an increase in porosity,leads to a discernible decline in proppant compressive strength.Intriguingly,upon crossing a porosity threshold of 10%,the decrement in strength becomes more gradual.A denser congregation of pores accelerates crack propagation,undermining proppant robustness,suggesting that under analogous conditions,hollow proppants might not match the strength of their porous counterparts.This exploration elucidates the underlying mechanisms of proppant failure from a microstructural perspective,furnishing pivotal insights that may guide future refinements in the architectural design of porous proppant.
基金supported by the National Natural Science Foundation of China(NSFC)(Nos.22178148 and 22278193)a Project Funded by the Priority Academic Program Development of Jiangsu Higher Education Institutions.
文摘As a catalyst of the air cathode in zinc-air batteries,tungstic acid ferrous(FeWO_(4)),a nanoscale transition metal tungstate,shows a broad application prospect in the oxygen reduction reaction(ORR).While FeWO_(4)possesses favorable electrochemical properties and thermodynamic stability,its intrinsic semiconductor characteristics result in a relatively slow electron transfer rate,limiting the ORR catalytic activity.In this work,the electronic structure of FeWO_(4)is significantly modulated by introducing phosphorus(P)atoms with abundant valence electrons.The P doping can adjust the electronic structure of FeWO_(4)and then optimize oxygen-containing intermediates'absorption/desorption efficiency to achieve improved ORR activity.Furthermore,the sodium chloride template is utilized to construct a porous carbon framework for anchoring phosphorus-doped iron tungstate(P-FeWO_(4)/PNC).The porous carbon skeleton provides numerous active sites for the absorption/desorption and redox reactions on the P-FeWO_(4)/PNC surface and serves as mass transport channels for reactants and intermediates.The P-FeWO_(4)/PNC demonstrates ORR performance(E1/2=0.86 V vs.RHE).Furthermore,the zinc-air batteries incorporating the P-FeWO_(4)/PNC composite demonstrate an increased peak power density(172.2 mW·cm^(-2)),high specific capacity(810.1 mAh·g^(-1)),and sustained long-term cycling stability lasting up to 240 h.This research not only contributes to the advancement of cost-effective tungsten-based non-precious metallic ORR catalysts,but also guides their utilization in zinc-air batteries.
基金financially supported by the National Key Research and Development Program of China(No.2022YFB4003801)the National Natural Science Foundation of China(No.52076091)We appreciate the analysis and characterization assistance of FESEM,XRD,and Raman from the Analytical and Testing Center at Huazhong University of Science&Technology.The author acknowledges the tubular furnace from Anhui Chem-n Instrument Co.,Ltd.
文摘Vanadium nitride(VN),a promising cathode material for aqueous zinc ion batteries(AZIBs),undergoes irreversible phase transitions accompanied by structural variation and sustained vanadium dissolution,which impair cycling stability and reaction kinetics.To address these challenges,we designed a core–shell heterostructure(VONC-T,T represents temperature)composed of a VN core and a porous carbon shell.This structure was synthesized via in-situ construction,involving optimized ratio of coating a zinc-based zeolitic imidazolate framework(ZIF-8)onto a vanadium-based metal-organic framework(MIL-47(V)),followed by a thermal treatment.This process ensures a high degree of interfacial stability between the core and shell,effectively mitigating the structural variation of VN during irreversible phase transitions and enhancing the overall structural stability.During thermal driving,the volatilization of zinc within the shell layer created a porous channel effect,which facilitating Zn^(2+)diffusion.The enhancement of Zn²⁺diffusion strengthens the efficient conversion of VN to amorphous VOx,labeled as VONC-T-a,which provides more active sites and consequently results in a high specific capacity.The optimized heterostructure of VONC-900-a presented high reversible capacity of 387.2 mAh g^(−1)at 0.2 A g^(−1)and demonstrated excellent rate performance,achieving 274.5 mAh g^(−1)at 20 A g^(−1),while maintaining a capacity retention rate of 93.3%after 5000 cycles at 10 A g^(−1).Density functional theory calculations confirmed improved reaction kinetics in the core–shell structure.This study not only highlights the potential of amorphous vanadium oxide core–shell heterostructure for AZIBs but also provides new insights into the conversion mechanisms of VN.
基金supported by the National Key R&D Program of China(No.2023YFB4603500)the Program for Innovation Team of Shaanxi Province(No.2023-CX-TD-17)+1 种基金the Fundamental Research Funds for the Central Universitiesthe Shaanxi Province Qinchuangyuan“Scientist+Engineer”Team Construction Project(No.2022KXJ-106).
文摘The bioinert nature of polyether ether ketone(PEEK)material limits the widespread clinical application of PEEK implants.Although the porous structure is considered to improve osseointegration of PEEK implants,it is hardly used due to its mechanical properties.This study investigated the combined influence of the porous structure and in vivo mechanical stimulation on implantation safety and bone growth based on finite element analysis of the biomechanical behavior of the implantation system.The combined control of pore size and screw preloads allows the porous PEEK implant to achieve good osseointegration while maintaining a relatively high safety level.A pore size of 600μm and a preload of 0.05 N·m are the optimal combination for the long-term stability of the implant,with which the safety factor of the implant is>2,and the predicted percentage of effective bone growth area of the bone-implant interface reaches 97%.For further clinical application,PEEK implants were fabricated with fused filament fabrication(FFF)three-dimensional(3D)printing,and clinical outcomes demonstrated better bone repair efficacy and long-term stability of porous PEEK implants compared to solid PEEK implants.Moreover,good osteointegration performance of 3D-printed porous PEEK implants was observed,with an average bone volume fraction>40%three months after implantation.In conclusion,3D-printed porous PEEK implants have great potential for clinical application,with validated implantation safety and good osseointegration.
基金financially supported by the National Natural Science Foundation of China(No.62105076)the Innovation Group of Guizhou University(No.[2024]08)+2 种基金the Platform of Science and Technology and Talent Team Plan of Guizhou Province(No.GCC[2023]007)the Guizhou Provincial Basic Research Program(No.ZK[2021]327)the Fok Ying Tung Education Foundation(No.171095)。
文摘Because of tempting magnetic-dielectric synergies and interfacial effects,designing a simple and low-cost route for producing multidimensional carbon-based magnetic nanocomposites is very important for the development of microwave absorbers(MAs).In this paper,a facile and propagable Ni-nitrilotriacetic acid chelate(NAC)derived strategy was proposed to selectively fabricate zero-dimensional(0D)/one-dimensional(1D)porous Ni/C magnetic heterostructured nanorods(MHNRs)consisting of 1D carbon nanorod,lots of pores and 0D Ni nanoparticles via a combined hydrothermal and thermally treated methods.The porous Ni/C MHNRs displayed the progressively improved Ni and C crystallinity by controlling the temperature,which resulted in the tunable electromagnetic and microwave absorption properties(MAPs).Additionally,0D/1D porous CoNi/C and Co/C MHNRs could be selectively produced through this strategy by adopting CoNi-NAC and Co-NAC as precursors.Benefiting from desirable interface and magnetic/dielectric synergies,the acquired 0D/1D porous Ni/C,CoNi/C and Co/C MHNRs presented excellent MAPs and certain corrosion resistance properties.In especial,Co/C MHNRs displayed a strong absorption capacity(−47.89 dB),an ultrawide effective absorption bandwidth(8.40 GHz)and small matching thicknesses(∼2 mm),which were a desirable candidate for MAs.Consequently,a facile,low-cost and propagable metal-NAC derived strategy was proposed to synthesize 0D/1D porous carbon-based MHNRs,which presented an alternative technique to develop lightweight efficient MAs.
基金the National Nature Science Foundation of China for Excellent Young Scientists Fund(32222058)Fundamental Research Foundation of CAF(CAFYBB2022QB001).
文摘Developing biomass platform compounds into high value-added chemicals is a key step in renewable resource utilization.Herein,we report porous carbon-supported Ni-ZnO nanoparticles catalyst(Ni-ZnO/AC)synthesized via low-temperature coprecipitation,exhibiting excellent performance for the selective hydrogenation of 5-hydroxymethylfurfural(HMF).A linear correlation is first observed between solvent polarity(E_(T)(30))and product selectivity within both polar aprotic and protic solvent classes,suggesting that solvent properties play a vital role in directing reaction pathways.Among these,1,4-dioxane(aprotic)favors the formation of 2,5-bis(hydroxymethyl)furan(BHMF)with 97.5%selectivity,while isopropanol(iPrOH,protic)promotes 2,5-dimethylfuran production with up to 99.5%selectivity.Mechanistic investigations further reveal that beyond polarity,proton-donating ability is critical in facilitating hydrodeoxygenation.iPrOH enables a hydrogen shuttle mechanism where protons assist in hydroxyl group removal,lowering the activation barrier.In contrast,1,4-dioxane,lacking hydrogen bond donors,stabilizes BHMF and hinders further conversion.Density functional theory calculations confirm a lower activation energy in iPrOH(0.60 eV)compared to 1,4-dioxane(1.07 eV).This work offers mechanistic insights and a practical strategy for solvent-mediated control of product selectivity in biomass hydrogenation,highlighting the decisive role of solvent-catalyst-substrate interactions.
基金supported by National Natural Science Foundation of China(No.52025055 and 52275571)Basic Research Operation Fund of China(No.xzy012024024).
文摘Tilted metasurface nanostructures,with excellent physical properties and enormous application potential,pose an urgent need for manufacturing methods.Here,electric-field-driven generative-nanoimprinting technique is proposed.The electric field applied between the template and the substrate drives the contact,tilting,filling,and holding processes.By accurately controlling the introduced included angle between the flexible template and the substrate,tilted nanostructures with a controllable angle are imprinted onto the substrate,although they are vertical on the template.By flexibly adjusting the electric field intensity and the included angle,large-area uniform-tilted,gradient-tilted,and high-angle-tilted nanostructures are fabricated.In contrast to traditional replication,the morphology of the nanoimprinting structure is extended to customized control.This work provides a cost-effective,efficient,and versatile technology for the fabrication of various large-area tilted metasurface structures.As an illustration,a tilted nanograting with a high coupling efficiency is fabricated and integrated into augmented reality displays,demonstrating superior imaging quality.
基金supported by the Research Project on Strengthening the Construction of an Important Ecological Security Barrier in Northern China by Higher Education Institutions in the Inner Mongolia Autonomous Region(STAQZX202313)the Inner Mongolia Autonomous Region Education Science‘14th Five-Year Plan’2024 Annual Research Project(NGJGH2024635).
文摘Vacancy defects,as fundamental disruptions in metallic lattices,play an important role in shaping the mechanical and electronic properties of aluminum crystals.However,the influence of vacancy position under coupled thermomechanical fields remains insufficiently understood.In this study,transmission and scanning electron microscopy were employed to observe dislocation structures and grain boundary heterogeneities in processed aluminum alloys,suggesting stress concentrations and microstructural inhomogeneities associated with vacancy accumulation.To complement these observations,first-principles calculations and molecular dynamics simulations were conducted for seven single-vacancy configurations in face-centered cubic aluminum.The stress response,total energy,density of states(DOS),and differential charge density were examined under varying compressive strain(ε=0–0.1)and temperature(0–600 K).The results indicate that face-centered vacancies tend to reduce mechanical strength and perturb electronic states near the Fermi level,whereas corner and edge vacancies appear to have weaker effects.Elevated temperatures may partially restore electronic uniformity through thermal excitation.Overall,these findings suggest that vacancy position exerts a critical but position-dependent influence on coupled structure-property relationships,offering theoretical insights and preliminary experimental support for defect-engineered aluminum alloy design.
基金Project(51146010)supported by the National Natural Science Foundation of ChinaProject(S2011040003189)supported by the Doctoral Research Fund of Guangdong Natural Science Foundation,ChinaProject supported by the Fundation of Key Laboratory of Surface Functional Structure Manufacturing of Guangdong Higher Education Institutes,South China University of Technology
文摘A solid-phase sintering process for the low-cost fabrication of composite micro-channels was developed. Three kinds of composite micro-channels with metallic porous structures were designed. The sintering process was studied and optimized to obtain porous-structured micro-channels with high porosity. The flow resistance and heat transfer performance in the composite micro-channels were investigated. The composite micro-channels show acceptable flow resistance, significant enhancement of heat transfer and dramatic improvement of flow boiling stability, which indicates a promising prospect for the application in forced convective heat transfer.
