Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synerg...Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synergy effects of interface-accelerating desolvation and spatial confinement have been demonstrated as the essential causation of this counterintuitive experimental phenomenon.At the molecular level,the imide ring(-CO-NR-CO-,in which R represents the phenyl)groups in an artificially introduced polyimide(PI)interlayer facilitate the strong electrostatic affinity towards Mg^(2+),which accelerates the desolvation process for Mg^(2+)solvation structures at the inner Helmholtz plane.At the nucleation scale,the wedge-like concave geometry formed at the PI/current collector interface provides energetically favorable sites for Mg nucleation.This unique architecture reduces the critical nucleus size,thereby significantly lowering nucleation energy barriers.As a result,the satisfactory Coulombic efficiency for Mg plating/stripping(98.22%)and cycle lifespan(1200 cycles,above 100 days)have been achieved,outperforming most of the previous results.This work pioneers a molecular-level understanding of separator-directed Mg deposition and resolves a long-standing confusion in Mg-metal batteries.展开更多
Recently, quantum Hall interface has become a popular subject of research;distinct from that of the quantum Hall edge, which is constrained by external background confinement, the interface has the freedom to move, li...Recently, quantum Hall interface has become a popular subject of research;distinct from that of the quantum Hall edge, which is constrained by external background confinement, the interface has the freedom to move, likely towards a string-like state. In disk geometry, it was known that the interface energy has an extra correction due to its curvature which depends on the size of the disk. In this work, we analytically calculate the energy of the integer quantum Hall interface on a cone surface which has the advantage of its curvature being more easily adjustable. By tuning the length and curvature of the interface by the cone angle parameter β, we analyze the dependence of the quantum Hall interface energy on the curvature and verify this geometric correction.Moreover, we find that the tip of the cone geometry has an extra contribution to the energy that reflects on the u_(2), u_(4) term.展开更多
Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purificatio...Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purification processes in modern industries.This study investigated the enhanced kinetic separatio n of target metal ions from complex aqueous solutio ns at a liquid-liquid interface,focusing on the presence of coexisting salt cations.Employing a typical thin-layer organic oil film(TOOF)extraction as a model system,the research examines how background Al^(3+)ions influence the mass transfer and separation of ions.Notably,the co ncentration of Al^(3+)ions affects both the distribution of Er^(3+)ions at the oil-water interface and the arrangement and orientation of P507 extractant molecules through the formation of unique hydrogen-bonding interactions.These interactions influence the selectivity of mass transfer,facilitating the separation of Er^(3+)from Al^(3+)ions.Specifically,the hydration shell of Er^(3+)ions is disrupted due to the strong hydration capability of coexisting Al^(3+)ions,leading to a higher interfacial concentration of Er^(3+)ions and a more ordered interfacial orientation of P507 molecules.At lower concentrations of Al^(3+)ions,the diffusion rate of Er^(3+)ions near the interface is high,enhancing the sepa ration perfo rmance of these ions.In contrast,at higher concentrations of Al^(3+)ions,the competitive hydration by Al^(3+)ions increases,and the interfacial concentration of Er^(3+)ions decreases due to enhanced diffusion resistance,resulting in poorer separation performance.Furthermore,a thinner membrane is more effective than a thicker one in enriching target Er^(3+)ions at the interface and achieving an ordered interfacial orientation of P507 molecules,thereby enhancing the separation coefficient(β_(Er/Al)).This work provides novel insights into the behaviors of ions and extractants at oil-wate r interface and the kinetic separation selectivity under varying concentrations of coexisting salt cations.展开更多
Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride he...Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures(denoted PtPdAu/BiTe)were synthesized using a visible-light-assisted strategy.The coupling alloy and interfacial effects of PtPdAu/BiTe significantly improved the performance and stability of both the ethanol oxidation reaction(EOR)and methanol oxidation reaction(MOR).Introducing a small amount of Au effectively enhanced the CO tolerance of PtPdAu/BiTe compared to dendritic platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures.PtPdAu/BiTe exhibited mass activities of 31.5 and 13.3 A·mg_(Pt)^(-1)in EOR and MOR,respectively,which were 34.4 and 13.2 times higher than those of commercial Pt black,revealing efficient Pt atom utilization.In-situ Fourier transform infrared spectroscopy demonstrated complete 12e^(-)and 6e^(-)oxidation of ethanol and methanol on PtPdAu/BiTe.The PtPdAu/BiTe/C achieved mass peak power densities of 131 and 156 mW·mg_(Pt)^(-1),which were 2.4 and 2.2 times higher than those of Pt/C in practical direct ethanol fuel cell(DEFC)and direct methanol fuel cell(DMFC),respectively,highlighting their potential application in DEFC and DMFC.This study introduces an effective strategy for designing efficient and highly CO tolerant anodic electrocatalysts for practical DEFC and DMFC applications.展开更多
Although the existence of glass–glass interfaces(GGIs)enables improved ductility of metallic nanoglasses(NGs),the excess free volumes at GGIs would cause the NGs to have a much-reduced mechanical strength.Herein,entr...Although the existence of glass–glass interfaces(GGIs)enables improved ductility of metallic nanoglasses(NGs),the excess free volumes at GGIs would cause the NGs to have a much-reduced mechanical strength.Herein,entropy-stabilized GGIs have been in-vestigated in Co–Fe–Ni–Zn–P NGs,which have a large entropy of mixing(1.32R,where R is the gas constant)and could be in a new glass phase,different from that of glassy grain interiors.Through quantitatively determining the activation energy of glass transition sep-arately for the GGIs and glassy grain interiors,the excess free volumes at GGIs are found to be reduced in comparison with those in the glassy grain interiors.The thermodynamically stable GGIs could be associated with increasing entropy of mixing in the GGI regions,which stabilizes the atomic structures of GGIs and enhances the glass forming ability of Co–Fe–Ni–Zn–P NGs.The influences of entropy-stabilized GGIs on the mechanical properties of Co–Fe–Ni–Zn–P NGs are further investigated by nanoindentation and creep tests under tensile deformation,demonstrating that there are notable enhancements in the ductility and mechanical strength for Co–Fe–Ni–Zn–P NGs.This work contributes to an in-depth understanding on the GGI phase in NGs and offers an alternative method for strengthening NGs through GGI engineering.展开更多
In order to maximize the advantages of high energy density in Li metal batteries,it is necessary to match cathode materials with high specific capacities.Ni-rich layered oxides have been shown to reversibly embed more...In order to maximize the advantages of high energy density in Li metal batteries,it is necessary to match cathode materials with high specific capacities.Ni-rich layered oxides have been shown to reversibly embed more Li+during charge and discharge processes due to the increased Ni content in their crystal structure,thereby providing higher energy density.However,a significant challenge associated with Ni-rich layered oxide cathodes is the crossover effect,which arises from the dissolution of Ni^(2+)from the cathode,leading to a rapid decline in battery capacity.Through the delocalization-induced effect of solvent molecules,Ni^(2+)is transformed into a fluorinated transition metal inorganic phase layer,thereby forming a corrosion-resistant Li metal interface.This prevents solvent molecules from being reduced and degraded by Li metal anode.The surface of the Li metal anode exhibits a smooth and flat deposition morphology after long-term cycling.Furthermore,the introduction of Ni^(2+)can enhance the concentration gradient of transition metal ions near the cathode,thereby suppressing the dissolution process of transition metal ions.Even the NCM955 cathode with a mass load of 22 mg cm^(−2)also has great capacity retention after cycling.The Ni^(2+)induced by high electronegative functional groups of solvent under the electron delocalization effect,preventing the Ni ions dissolution of cathode and constructing a corrosion-resistant Li metal interface layer.This work provides new insights into suppressing crossover effects in Li metal batteries with high nickel cathodes.展开更多
Based on the theoretical representation of piezoelectric quasicrystal,a generalized dynamic model is built to represent the transmission of wave aspects in surface acoustic pulse nano-devices.Surface elasticity,surfac...Based on the theoretical representation of piezoelectric quasicrystal,a generalized dynamic model is built to represent the transmission of wave aspects in surface acoustic pulse nano-devices.Surface elasticity,surface piezoelectricity,and surface permittivity help to include the surface effect,which equals additional thin sheets.It is shown that,under certain assumptions,this generalized dynamic model may be simplified to a few classical examples that are appropriate for both macro and nano-scale applications.In the current work,surface piezoelectricity is used to develop a theoretical model for shear horizontal(SH)waves where it contains the surface piezoelectricity theory and a linear spring model to quantitatively and qualitatively explore SH waves in an orthotropic piezoelectric quasicrystal layer overlying an elastic framework(Model I),a piezoelectric quasi-crystal nano substrate,and an orthotropic piezoelectric quasicrystal half-space(Model II).The theoretical model stimulates the numerical results,which establish the critical thickness.As the piezoelectric layer’s thickness gets closer to nanometres,surface energy must be included when analyzing dispersion properties.Furthermore,the effects of surface elasticity and density on wave velocity are investigated individually.The authors establish a parameter,precisely the ratio of the physical modulus along the width direction to along the direction of wave travel.The surface effect’s impact on the general char-acteristics of piezoelectric structures is seen as a spring force acting on bulk boundaries.Analytical presentation of frequency equations for both symmetric and anti-symmetric waves pertains to the case of an electrical short circuit in Model II.The project aims to analyze SH waves in orthogonal anisotropic,transversely isotropic piezoelectric layered nanostructures,providing a practical mathematical tool for surface effects analysis and adaptability to other wave types,including Rayleigh waves and acoustic surface waves.展开更多
Two-dimensional （2D） equations for multiferroic （MF） laminated plates with imperfect interfaces are established in this paper. The interface between two adjacent sublayers, which are not perfectly bonded together,...Two-dimensional （2D） equations for multiferroic （MF） laminated plates with imperfect interfaces are established in this paper. The interface between two adjacent sublayers, which are not perfectly bonded together, is modeled as a general spring-type layer. The mechanical displacements, and the electric and magnetic potentials of the two adjacent layers are assumed to be discontinuous at the interface. As an example, the influences of imperfect interfaces on the magnetoelectric （ME） coupling effects in an MF sandwich plate are investigated with the established 2D governing equations. Numerical results show that the imperfect interfaces have a significant impact on the ME coupling effects in MF laminated structures.展开更多
The influence of melt superheating treatment on the solid/liquid （S/L） interface morphology of directionally solidified Ni-based superalloy DZ125 is investigated to elucidate the relationship between melt characteri...The influence of melt superheating treatment on the solid/liquid （S/L） interface morphology of directionally solidified Ni-based superalloy DZ125 is investigated to elucidate the relationship between melt characteristic and S/L interface stability. The results indicate that the interface morphology is not only related to the withdrawal velocity （R） but also to the melt superheating temperature （Ts） when the thermal gradient of solidification interface remains constant for different Ts with appropriate superheating treatment regulation. The interface morphology changes from cell to plane at R of 1.1 μm/s when Ts increases from 1500°C to 1650°C, and maintains plane with further elevated Ts of 1750°C. However, the interface morphology changes from coarse dendrite to cell and then to cellular dendrite at R of 2.25 μm/s when Ts increases from 1500°C to 1650°C and then to 1750°C. It is proved that the solidification onset temperature and the solidification interval undergo the nonlinear variation when Ts increases from 1500°C to 1680°C, and the turning point is 1650°C at which the solidification onset temperature and the solidification interval are all minimum. This indicates that the melt superheating treatment enhances the solidification interface stability and has important effect on the solidification characteristics.展开更多
Ferromanganese crusts and nodules are important submarine mineral resources that contain various metal elements with significant economic value. In this study, polymetallic crusts and nodules obtained from the South C...Ferromanganese crusts and nodules are important submarine mineral resources that contain various metal elements with significant economic value. In this study, polymetallic crusts and nodules obtained from the South China Sea （SCS） were determined by using X-ray power diffraction （XRD）, Raman spectroscopy （RS）, Fourier transform infrared spectroscopy （FTIR）, and X-ray photoelectron spectroscopy （XPS） to systematically investigate and analyze the mineralogical and spectral characteristics of the Fe-Mn minerals. XRD measurements revealed that the SCS polymetallic crusts and nodules were composed of vernadite, quartz, and plagioclase. The nodules also contained todorokite. The Fe-phase minerals of the SCS crusts and nodules were composed of amorphous Fe oxide/hydroxide, and the Mn- and Fe-phases minerals exhibited relatively poor degrees of crystallization. FTIR results showed that the Fe-Mn minerals in the crusts and nodules included a large number of surface hydroxyl groups. These surface hydroxyl groups contained protons that could provide reactive sites for complexation of ore-forming elements in seawater. XPS results indicated that the surfaces of the Fe-Mn minerals mainly contained Fe, Mn, and O. Fe was present in the trivalent oxidation state, while Mn, which may contain several bivalent oxidation state, was present in the tetravalent and trivalent oxidation states. The SCS polymetallic crusts and nodules were compared with Pacific seamount crusts, and results showed that the surface hydroxyl （-OH） groups of the SCS crusts and nodules numbered more than the lattice oxygen （O^2-）. But the lattice oxygen of Pacific seamount crusts numbered more than the surface hydroxyl groups. This characteristic indicated that the degree of crystallization of Fe-Mn minerals from the Pacific Ocean was higher than that of minerals from the South China Sea. Comprehensive studies showed that ore-forming elements in the interface between seawater and the Fe-Mn minerals in the submarine ferromanganese crusts and nodules employed the following enrichment mechanisms： （1） the metal ion complexed with the surface hydroxyl of Fe-Mn minerals to form hydroxyl complexes, which were connected by coordination bonds or stable inner-sphere complexes that exchanged protons on the mineral surfaces; （2） the charged surfaces of the minerals and metal cations formed outer-sphere complexes, which made up the electrostatic double layer, through electrostatic adsorption; and （3） the metal cations isomorphously exchanged the Mn and Fe ions of the mineral lattice structure.展开更多
Inhibiting the “shuttle effect” of soluble polysulfides and improving reaction kinetics are the key factors necessary for further exploration of high-performance Li-S batteries. Herein, an effective interface engine...Inhibiting the “shuttle effect” of soluble polysulfides and improving reaction kinetics are the key factors necessary for further exploration of high-performance Li-S batteries. Herein, an effective interface engineering strategy is reported, wherein nitriding of an Ni-based precursor is controlled to enhance Li-S cell regulation. The resulting in-situ formed NiO-Ni_(3)N heterostructure interface not only has a stronger polysulfide adsorption effect than that of monomeric NiO or Ni_(3)N but also has a faster Li ion diffusion ability than a simple physical mixture. More importantly, this approach couples the respective advantages of NiO and Ni_(3)N to reduce polarization and facilitate electron transfer during polysulfide reactions and synergistically catalyze polysulfide conversion. In addition, ultrafine nanoparticles are thought to effectively improve the use of additive materials. In summary, Li-S batteries based on this NiO-Ni_(3)N heterostructure have the features of long cycle stability, rapid charging-discharging, and good performance under high sulfur loading.展开更多
The high-temperature mechanical behaviors of Multi-Layer Composite Panels(MCP)and Corrugated Sandwich Panels(CSP)of Continuous Glass Fiber-Reinforced Polypropylene(CGFRPP)are critical for their application in aerospac...The high-temperature mechanical behaviors of Multi-Layer Composite Panels(MCP)and Corrugated Sandwich Panels(CSP)of Continuous Glass Fiber-Reinforced Polypropylene(CGFRPP)are critical for their application in aerospace fields,which have been rarely mentioned in previous studies.High-temperature quasi-static tensile and compression tests on CGFRPP MCP are conducted first.The results showed that the tensile and compression strength,stiffness,and tensile modulus of MCP decreased with increasing temperature.The Gibson model was found to be more suitable for predicting the high-temperature mechanical performance of MCP after comparing the calculated results of different theoretical models with experimental data.Secondly,hightemperature planar compression tests were conducted on the CGFRPP CSP,revealing that the main failure modes were corrugated core buckling and delamination between the face panel and core material,with delamination being intensified at higher temperatures.Therefore,we proposed a strength theoretical model that considers structural buckling failure and interface delamination failure,and introduced the influence factor to evaluate the effect of interface delamination on structural strength.展开更多
In terfaces that exist in composites greatly influence their mechanical and conductive properties.There are usually three interface models to characterize the elastic and conductive properties of the interface in comp...In terfaces that exist in composites greatly influence their mechanical and conductive properties.There are usually three interface models to characterize the elastic and conductive properties of the interface in composites.For elastic problems,they are the interface stress model(ISM),linear spring model(LSM),and interphase model.For conductive problems,they are the high conducting(HC)interface model,low conducting(LC)interface model,and interphase model.For elastic problems with the interface effects,they can be divided into two types.The first kind of elastic problem concerns the solution of boundary value problems and aims to predict the effective properties of composites with interface effects.The second kind of elastic problem concerns the surface/interface stress effects on the elastic properties of nanostructured materials,which is usually characterized by the ISM.In this paper,three aspects in the elastic problems with interface effects are first reviewed,i.e.,equivalent relations among the three interface models,Eshelby formalism,and micromechanical frameworks.Special emphasis is placed on the ISM to show how classical models can be extended to the nano-scale by supplementing the interface elasticity to the basic equations of the classical elastic problems.Then,the conductive problems of the composites with the interface effects are also reviewed,and the general frameworks for predicting the effective conductivity of the composites are given.Finally,scaling laws depicting the size-dependent elastic and conductive properties of the composites are discussed.展开更多
Interface and scale effects are the two most important factors which strongly affect the structure and the properties of nano-/micro-crystals under pressure.We conduct an experiment under high pressure in situ alterna...Interface and scale effects are the two most important factors which strongly affect the structure and the properties of nano-/micro-crystals under pressure.We conduct an experiment under high pressure in situ alternating current impedance to elucidate the effects of interface on the structure and electrical transport behavior of two Zn Se samples with different sizes obtained by physical grinding.The results show that（i） two different-sized Zn Se samples undergo the same phase transitions from zinc blend to cinnabar-type phase and then to rock salt phase;（ii） the structural transition pressure of the859-nm Zn Se sample is higher than that of the sample of 478 nm,which indicates the strong scale effect.The pressure induced boundary resistance change is obtained by fitting the impedance spectrum,which shows that the boundary conduction dominates the electrical transport behavior of Zn Se in the whole experimental pressure range.By comparing the impedance spectra of two different-sized Zn Se samples at high pressure,we find that the resistance of the 478-nm Zn Se sample is lower than that of the 859-nm sample,which illustrates that the sample with smaller particle size has more defects which are due to physical grinding.展开更多
Classical micromechanical methods for calculating the effective moduli of a heteroge- neous material are generalized to include the interface(surface)effect.By using Hashin's Composite Sphere Assemblage(CSA)model,...Classical micromechanical methods for calculating the effective moduli of a heteroge- neous material are generalized to include the interface(surface)effect.By using Hashin's Composite Sphere Assemblage(CSA)model,a new expression of the bulk modulus for a particle-reinforced com- posite is derived.It is emphasized that the present study is within the finite-deformation framework such that the effective properties are not influenced by the interface stress itself solely,but influenced by the change of the interface stress due to changes of the shape and size of the interface.Hence some inadequacies in previous papers are pointed out.展开更多
The salt effects on molecular orientation at air/liquid methanol interface were investigated by the polarization-dependent sum frequency generation vibrational spectroscopy（SFG-VS）. We clarified that the average til...The salt effects on molecular orientation at air/liquid methanol interface were investigated by the polarization-dependent sum frequency generation vibrational spectroscopy（SFG-VS）. We clarified that the average tilting angle of the methyl group to be u = 308 58 at the air/pure methanol surface assuming a d-function orientational distribution. Upon the addition of 3 mol/L Na I, the methyl group tilts further away from the surface normal with a new u = 418 38. This orientational change does not explain the enhancement of the SFG-VS intensities when adding Na I, implying the number density of the methanol molecules with a net polar ordering in the surface region also changed with the Na I concentrations. These spectroscopic findings shed new light on the salt effects on the surfaces structures of the polar organic solutions. It was also shown that the accurate determination of the bulk refractive indices and Raman depolarization ratios for different salt concentrations is crucial to quantitatively interpret the SFG-VS data.展开更多
The dependences of Fermi-level pinning on interface state densities for the metal-dielectric, ploycrystalline silicon-dielectric, and metal silicide-dielectric interfaces are investigated by calculating their effectiv...The dependences of Fermi-level pinning on interface state densities for the metal-dielectric, ploycrystalline silicon-dielectric, and metal silicide-dielectric interfaces are investigated by calculating their effective work functions and their pinning factors. The Fermi-level pinning factors and effective work functions of the metal-dielectric interface are observed to be more susceptible to the increasing interface state densities, differing significantly from that of the ploycrystalline silicon-dielectric interface and the metal silicide-dielectric interface. The calculation results indicate that metal silicide gates with high-temperature resistance and low resistivity are a more promising choice for the design of gate materials in metal-oxide semiconductor（MOS） technology.展开更多
The catalytic performance of Molybdenum disulfide(MoS_(2)) has been still far from that of Pt-based catalysts for inadequate active sites and sluggish electron transfer kinetics. Through engineering the interface betw...The catalytic performance of Molybdenum disulfide(MoS_(2)) has been still far from that of Pt-based catalysts for inadequate active sites and sluggish electron transfer kinetics. Through engineering the interface between MoS_(2)-based materials and supported substrates, hybrid Ru-doped MoS_(2) on carbonized lignin(CL) is designed and prepared as efficient catalyst for hydrogen evolution reaction(HER). The CL substrate not only facilitates the growth of MoS_(2) nanoflowers, but also promotes the electron transfer. Ru doping increases active sites greatly for HER. The hybrid catalyst achieves a low onset overpotential of 25 mV and a low Tafel slope of 46 m V dec^(-1). The favorable HER activity ascribes to the interfacial interaction between MoS_(2) and CL. Density functional theory calculations further confirm the improved HER performance with doped Ru atoms. This study presents a prototype application to design electrocatalysts with enhanced carrier mobility and high-density active sites based on interface effect.展开更多
基金supported by the National Natural Science Foundation of China(22279068,52374306)the Taishan Scholars of Shandong Province(tsqn202408202)the Qingdao New Energy Shandong Laboratory Open Project(QNESL OP202312)。
文摘Preferential magnesium(Mg)electrodeposition on separators is a ubiquitous yet poorly understood phenomenon in rechargeable Mg-metal batteries,posing a fundamental challenge to their development.In this work,the synergy effects of interface-accelerating desolvation and spatial confinement have been demonstrated as the essential causation of this counterintuitive experimental phenomenon.At the molecular level,the imide ring(-CO-NR-CO-,in which R represents the phenyl)groups in an artificially introduced polyimide(PI)interlayer facilitate the strong electrostatic affinity towards Mg^(2+),which accelerates the desolvation process for Mg^(2+)solvation structures at the inner Helmholtz plane.At the nucleation scale,the wedge-like concave geometry formed at the PI/current collector interface provides energetically favorable sites for Mg nucleation.This unique architecture reduces the critical nucleus size,thereby significantly lowering nucleation energy barriers.As a result,the satisfactory Coulombic efficiency for Mg plating/stripping(98.22%)and cycle lifespan(1200 cycles,above 100 days)have been achieved,outperforming most of the previous results.This work pioneers a molecular-level understanding of separator-directed Mg deposition and resolves a long-standing confusion in Mg-metal batteries.
基金supported by the National Natural Science Foundation of China under Grant Nos. 12347101 and 12474140the Fundamental Research Funds for the Central Universities under Grant No. 2024CDJXY022+3 种基金supported by National Natural Science Foundation of China under Grant No. 61988102The Key Research and Development Program of Guangdong Province under Grant No. 2019B090917007the Science and Technology Planning Project of Guangdong Province under Grant No. 2019B090909011Guangdong Provincial Key Laboratory under Grant No. 2019B121203002。
文摘Recently, quantum Hall interface has become a popular subject of research;distinct from that of the quantum Hall edge, which is constrained by external background confinement, the interface has the freedom to move, likely towards a string-like state. In disk geometry, it was known that the interface energy has an extra correction due to its curvature which depends on the size of the disk. In this work, we analytically calculate the energy of the integer quantum Hall interface on a cone surface which has the advantage of its curvature being more easily adjustable. By tuning the length and curvature of the interface by the cone angle parameter β, we analyze the dependence of the quantum Hall interface energy on the curvature and verify this geometric correction.Moreover, we find that the tip of the cone geometry has an extra contribution to the energy that reflects on the u_(2), u_(4) term.
基金Project supported by the National Natural Science Foundation of China(52074031,51574213,51904027)the Fundamental Research Funds for the Central Universities of China(06500104)。
文摘Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purification processes in modern industries.This study investigated the enhanced kinetic separatio n of target metal ions from complex aqueous solutio ns at a liquid-liquid interface,focusing on the presence of coexisting salt cations.Employing a typical thin-layer organic oil film(TOOF)extraction as a model system,the research examines how background Al^(3+)ions influence the mass transfer and separation of ions.Notably,the co ncentration of Al^(3+)ions affects both the distribution of Er^(3+)ions at the oil-water interface and the arrangement and orientation of P507 extractant molecules through the formation of unique hydrogen-bonding interactions.These interactions influence the selectivity of mass transfer,facilitating the separation of Er^(3+)from Al^(3+)ions.Specifically,the hydration shell of Er^(3+)ions is disrupted due to the strong hydration capability of coexisting Al^(3+)ions,leading to a higher interfacial concentration of Er^(3+)ions and a more ordered interfacial orientation of P507 molecules.At lower concentrations of Al^(3+)ions,the diffusion rate of Er^(3+)ions near the interface is high,enhancing the sepa ration perfo rmance of these ions.In contrast,at higher concentrations of Al^(3+)ions,the competitive hydration by Al^(3+)ions increases,and the interfacial concentration of Er^(3+)ions decreases due to enhanced diffusion resistance,resulting in poorer separation performance.Furthermore,a thinner membrane is more effective than a thicker one in enriching target Er^(3+)ions at the interface and achieving an ordered interfacial orientation of P507 molecules,thereby enhancing the separation coefficient(β_(Er/Al)).This work provides novel insights into the behaviors of ions and extractants at oil-wate r interface and the kinetic separation selectivity under varying concentrations of coexisting salt cations.
基金supported by the National Natural Science Foundation of China(No.22465009)the Education Department of Guizhou Province(No.2021312)the Foundation of Guizhou Province(No.2019-5666).
文摘Alloying and interface effects are effective strategies for enhancing the performance of electrocatalysts in energy-related devices.Herein,dendritic Au-doped platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures(denoted PtPdAu/BiTe)were synthesized using a visible-light-assisted strategy.The coupling alloy and interfacial effects of PtPdAu/BiTe significantly improved the performance and stability of both the ethanol oxidation reaction(EOR)and methanol oxidation reaction(MOR).Introducing a small amount of Au effectively enhanced the CO tolerance of PtPdAu/BiTe compared to dendritic platinum-palladium alloy/dumbbell-like bismuth telluride heterostructures.PtPdAu/BiTe exhibited mass activities of 31.5 and 13.3 A·mg_(Pt)^(-1)in EOR and MOR,respectively,which were 34.4 and 13.2 times higher than those of commercial Pt black,revealing efficient Pt atom utilization.In-situ Fourier transform infrared spectroscopy demonstrated complete 12e^(-)and 6e^(-)oxidation of ethanol and methanol on PtPdAu/BiTe.The PtPdAu/BiTe/C achieved mass peak power densities of 131 and 156 mW·mg_(Pt)^(-1),which were 2.4 and 2.2 times higher than those of Pt/C in practical direct ethanol fuel cell(DEFC)and direct methanol fuel cell(DMFC),respectively,highlighting their potential application in DEFC and DMFC.This study introduces an effective strategy for designing efficient and highly CO tolerant anodic electrocatalysts for practical DEFC and DMFC applications.
基金This work has been endorsed by the Chengdu Guangming Paite Precious Metal Co.,Ltd.,the CDGM Glass Co.,Ltd.,China,and the Research Grants Council of Hong Kong Special Administrative Region,China(No.15233823).
文摘Although the existence of glass–glass interfaces(GGIs)enables improved ductility of metallic nanoglasses(NGs),the excess free volumes at GGIs would cause the NGs to have a much-reduced mechanical strength.Herein,entropy-stabilized GGIs have been in-vestigated in Co–Fe–Ni–Zn–P NGs,which have a large entropy of mixing(1.32R,where R is the gas constant)and could be in a new glass phase,different from that of glassy grain interiors.Through quantitatively determining the activation energy of glass transition sep-arately for the GGIs and glassy grain interiors,the excess free volumes at GGIs are found to be reduced in comparison with those in the glassy grain interiors.The thermodynamically stable GGIs could be associated with increasing entropy of mixing in the GGI regions,which stabilizes the atomic structures of GGIs and enhances the glass forming ability of Co–Fe–Ni–Zn–P NGs.The influences of entropy-stabilized GGIs on the mechanical properties of Co–Fe–Ni–Zn–P NGs are further investigated by nanoindentation and creep tests under tensile deformation,demonstrating that there are notable enhancements in the ductility and mechanical strength for Co–Fe–Ni–Zn–P NGs.This work contributes to an in-depth understanding on the GGI phase in NGs and offers an alternative method for strengthening NGs through GGI engineering.
基金the support from Yunnan Fundamental Research Projects(202301BE070001-029,202401CF070129,202501CF070181)National Natural Science Foundation of China(22209012,22479067)Kunming University of Science and Technology Analysis and Testing Fund Support Project(2023T20220172)。
文摘In order to maximize the advantages of high energy density in Li metal batteries,it is necessary to match cathode materials with high specific capacities.Ni-rich layered oxides have been shown to reversibly embed more Li+during charge and discharge processes due to the increased Ni content in their crystal structure,thereby providing higher energy density.However,a significant challenge associated with Ni-rich layered oxide cathodes is the crossover effect,which arises from the dissolution of Ni^(2+)from the cathode,leading to a rapid decline in battery capacity.Through the delocalization-induced effect of solvent molecules,Ni^(2+)is transformed into a fluorinated transition metal inorganic phase layer,thereby forming a corrosion-resistant Li metal interface.This prevents solvent molecules from being reduced and degraded by Li metal anode.The surface of the Li metal anode exhibits a smooth and flat deposition morphology after long-term cycling.Furthermore,the introduction of Ni^(2+)can enhance the concentration gradient of transition metal ions near the cathode,thereby suppressing the dissolution process of transition metal ions.Even the NCM955 cathode with a mass load of 22 mg cm^(−2)also has great capacity retention after cycling.The Ni^(2+)induced by high electronegative functional groups of solvent under the electron delocalization effect,preventing the Ni ions dissolution of cathode and constructing a corrosion-resistant Li metal interface layer.This work provides new insights into suppressing crossover effects in Li metal batteries with high nickel cathodes.
文摘Based on the theoretical representation of piezoelectric quasicrystal,a generalized dynamic model is built to represent the transmission of wave aspects in surface acoustic pulse nano-devices.Surface elasticity,surface piezoelectricity,and surface permittivity help to include the surface effect,which equals additional thin sheets.It is shown that,under certain assumptions,this generalized dynamic model may be simplified to a few classical examples that are appropriate for both macro and nano-scale applications.In the current work,surface piezoelectricity is used to develop a theoretical model for shear horizontal(SH)waves where it contains the surface piezoelectricity theory and a linear spring model to quantitatively and qualitatively explore SH waves in an orthotropic piezoelectric quasicrystal layer overlying an elastic framework(Model I),a piezoelectric quasi-crystal nano substrate,and an orthotropic piezoelectric quasicrystal half-space(Model II).The theoretical model stimulates the numerical results,which establish the critical thickness.As the piezoelectric layer’s thickness gets closer to nanometres,surface energy must be included when analyzing dispersion properties.Furthermore,the effects of surface elasticity and density on wave velocity are investigated individually.The authors establish a parameter,precisely the ratio of the physical modulus along the width direction to along the direction of wave travel.The surface effect’s impact on the general char-acteristics of piezoelectric structures is seen as a spring force acting on bulk boundaries.Analytical presentation of frequency equations for both symmetric and anti-symmetric waves pertains to the case of an electrical short circuit in Model II.The project aims to analyze SH waves in orthogonal anisotropic,transversely isotropic piezoelectric layered nanostructures,providing a practical mathematical tool for surface effects analysis and adaptability to other wave types,including Rayleigh waves and acoustic surface waves.
基金supported by the National Natural Science Foundation of China(11672265,11202182,11272281,11621062,and 11321202)the Fundamental Research Funds for the Central Universities(2016QNA4026 and 2016XZZX001-05)the open foundation of Zhejiang Provincial Top Key Discipline of Mechanical Engineering
文摘Two-dimensional （2D） equations for multiferroic （MF） laminated plates with imperfect interfaces are established in this paper. The interface between two adjacent sublayers, which are not perfectly bonded together, is modeled as a general spring-type layer. The mechanical displacements, and the electric and magnetic potentials of the two adjacent layers are assumed to be discontinuous at the interface. As an example, the influences of imperfect interfaces on the magnetoelectric （ME） coupling effects in an MF sandwich plate are investigated with the established 2D governing equations. Numerical results show that the imperfect interfaces have a significant impact on the ME coupling effects in MF laminated structures.
基金supports from the National Natural Science Foundation of China (Grant No. 50931004)the National Basic Research Program of China (Grant Nos. 2011CB610406 and 2010CB631202)the National High Technology Research and Development Program (Grant No. 2007AA03Z552)
文摘The influence of melt superheating treatment on the solid/liquid （S/L） interface morphology of directionally solidified Ni-based superalloy DZ125 is investigated to elucidate the relationship between melt characteristic and S/L interface stability. The results indicate that the interface morphology is not only related to the withdrawal velocity （R） but also to the melt superheating temperature （Ts） when the thermal gradient of solidification interface remains constant for different Ts with appropriate superheating treatment regulation. The interface morphology changes from cell to plane at R of 1.1 μm/s when Ts increases from 1500°C to 1650°C, and maintains plane with further elevated Ts of 1750°C. However, the interface morphology changes from coarse dendrite to cell and then to cellular dendrite at R of 2.25 μm/s when Ts increases from 1500°C to 1650°C and then to 1750°C. It is proved that the solidification onset temperature and the solidification interval undergo the nonlinear variation when Ts increases from 1500°C to 1680°C, and the turning point is 1650°C at which the solidification onset temperature and the solidification interval are all minimum. This indicates that the melt superheating treatment enhances the solidification interface stability and has important effect on the solidification characteristics.
基金The National Natural Science Foundation of China under contract Nos 40473024 and 40343019the research fund from State Key Laboratory for Mineral Deposits Research in Nanjing University under contract No.20-15-07+3 种基金the Investigation and Development of Marine Resources during the 12th Five Year Plan Project under contract No.DY125-13-R-05the Doctoral Program of Higher Education Research Fund under contract Nos 20040558049 and 20120171130005the Project of High Level Talents in Colleges of Guangdong Province(2011)the Fundamental Research Funds for Central Universities under contract Nos 16lgjc11,12lgjc05 and 09lgpy09
文摘Ferromanganese crusts and nodules are important submarine mineral resources that contain various metal elements with significant economic value. In this study, polymetallic crusts and nodules obtained from the South China Sea （SCS） were determined by using X-ray power diffraction （XRD）, Raman spectroscopy （RS）, Fourier transform infrared spectroscopy （FTIR）, and X-ray photoelectron spectroscopy （XPS） to systematically investigate and analyze the mineralogical and spectral characteristics of the Fe-Mn minerals. XRD measurements revealed that the SCS polymetallic crusts and nodules were composed of vernadite, quartz, and plagioclase. The nodules also contained todorokite. The Fe-phase minerals of the SCS crusts and nodules were composed of amorphous Fe oxide/hydroxide, and the Mn- and Fe-phases minerals exhibited relatively poor degrees of crystallization. FTIR results showed that the Fe-Mn minerals in the crusts and nodules included a large number of surface hydroxyl groups. These surface hydroxyl groups contained protons that could provide reactive sites for complexation of ore-forming elements in seawater. XPS results indicated that the surfaces of the Fe-Mn minerals mainly contained Fe, Mn, and O. Fe was present in the trivalent oxidation state, while Mn, which may contain several bivalent oxidation state, was present in the tetravalent and trivalent oxidation states. The SCS polymetallic crusts and nodules were compared with Pacific seamount crusts, and results showed that the surface hydroxyl （-OH） groups of the SCS crusts and nodules numbered more than the lattice oxygen （O^2-）. But the lattice oxygen of Pacific seamount crusts numbered more than the surface hydroxyl groups. This characteristic indicated that the degree of crystallization of Fe-Mn minerals from the Pacific Ocean was higher than that of minerals from the South China Sea. Comprehensive studies showed that ore-forming elements in the interface between seawater and the Fe-Mn minerals in the submarine ferromanganese crusts and nodules employed the following enrichment mechanisms： （1） the metal ion complexed with the surface hydroxyl of Fe-Mn minerals to form hydroxyl complexes, which were connected by coordination bonds or stable inner-sphere complexes that exchanged protons on the mineral surfaces; （2） the charged surfaces of the minerals and metal cations formed outer-sphere complexes, which made up the electrostatic double layer, through electrostatic adsorption; and （3） the metal cations isomorphously exchanged the Mn and Fe ions of the mineral lattice structure.
基金financial support of the Youth Project of the Provincial Natural Science Foundation of Anhui(No. 2008085QE267)the Doctoral Research Initiation Foundation of Anhui Normal University (No. 751973)+2 种基金the National Natural Science Foundation of China (No. 51972162)the Fundamental Research Funds for the Central Universities (No. 0213-14380196)the Science and Technology Project of Nanchang (No. 2017-SJSYS-008)。
文摘Inhibiting the “shuttle effect” of soluble polysulfides and improving reaction kinetics are the key factors necessary for further exploration of high-performance Li-S batteries. Herein, an effective interface engineering strategy is reported, wherein nitriding of an Ni-based precursor is controlled to enhance Li-S cell regulation. The resulting in-situ formed NiO-Ni_(3)N heterostructure interface not only has a stronger polysulfide adsorption effect than that of monomeric NiO or Ni_(3)N but also has a faster Li ion diffusion ability than a simple physical mixture. More importantly, this approach couples the respective advantages of NiO and Ni_(3)N to reduce polarization and facilitate electron transfer during polysulfide reactions and synergistically catalyze polysulfide conversion. In addition, ultrafine nanoparticles are thought to effectively improve the use of additive materials. In summary, Li-S batteries based on this NiO-Ni_(3)N heterostructure have the features of long cycle stability, rapid charging-discharging, and good performance under high sulfur loading.
基金co-supported by the National Natural Science Foundation of China(Nos.12372127,12202085,12302464)the Fundamental Research Funds for the Central Universities,China(No.2024CDJXY009)+1 种基金the Chongqing Outstanding Youth Fund,China(No.CSTB2024NSCQ-JQX0028)the Chongqing Natural Science Foundation,China(Nos.cstc2021ycjh-bgzxm0117,CSTB2022NSCQ-MSX0608)。
文摘The high-temperature mechanical behaviors of Multi-Layer Composite Panels(MCP)and Corrugated Sandwich Panels(CSP)of Continuous Glass Fiber-Reinforced Polypropylene(CGFRPP)are critical for their application in aerospace fields,which have been rarely mentioned in previous studies.High-temperature quasi-static tensile and compression tests on CGFRPP MCP are conducted first.The results showed that the tensile and compression strength,stiffness,and tensile modulus of MCP decreased with increasing temperature.The Gibson model was found to be more suitable for predicting the high-temperature mechanical performance of MCP after comparing the calculated results of different theoretical models with experimental data.Secondly,hightemperature planar compression tests were conducted on the CGFRPP CSP,revealing that the main failure modes were corrugated core buckling and delamination between the face panel and core material,with delamination being intensified at higher temperatures.Therefore,we proposed a strength theoretical model that considers structural buckling failure and interface delamination failure,and introduced the influence factor to evaluate the effect of interface delamination on structural strength.
基金the National Natural Science Foundation of China(Grant Nos.11988102,11872004,and 91848201).
文摘In terfaces that exist in composites greatly influence their mechanical and conductive properties.There are usually three interface models to characterize the elastic and conductive properties of the interface in composites.For elastic problems,they are the interface stress model(ISM),linear spring model(LSM),and interphase model.For conductive problems,they are the high conducting(HC)interface model,low conducting(LC)interface model,and interphase model.For elastic problems with the interface effects,they can be divided into two types.The first kind of elastic problem concerns the solution of boundary value problems and aims to predict the effective properties of composites with interface effects.The second kind of elastic problem concerns the surface/interface stress effects on the elastic properties of nanostructured materials,which is usually characterized by the ISM.In this paper,three aspects in the elastic problems with interface effects are first reviewed,i.e.,equivalent relations among the three interface models,Eshelby formalism,and micromechanical frameworks.Special emphasis is placed on the ISM to show how classical models can be extended to the nano-scale by supplementing the interface elasticity to the basic equations of the classical elastic problems.Then,the conductive problems of the composites with the interface effects are also reviewed,and the general frameworks for predicting the effective conductivity of the composites are given.Finally,scaling laws depicting the size-dependent elastic and conductive properties of the composites are discussed.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.11404133 and 11374121)the Program of Science and Technology Development Plan of Jilin Province,China(Grant No.20140520105JH)
文摘Interface and scale effects are the two most important factors which strongly affect the structure and the properties of nano-/micro-crystals under pressure.We conduct an experiment under high pressure in situ alternating current impedance to elucidate the effects of interface on the structure and electrical transport behavior of two Zn Se samples with different sizes obtained by physical grinding.The results show that（i） two different-sized Zn Se samples undergo the same phase transitions from zinc blend to cinnabar-type phase and then to rock salt phase;（ii） the structural transition pressure of the859-nm Zn Se sample is higher than that of the sample of 478 nm,which indicates the strong scale effect.The pressure induced boundary resistance change is obtained by fitting the impedance spectrum,which shows that the boundary conduction dominates the electrical transport behavior of Zn Se in the whole experimental pressure range.By comparing the impedance spectra of two different-sized Zn Se samples at high pressure,we find that the resistance of the 478-nm Zn Se sample is lower than that of the 859-nm sample,which illustrates that the sample with smaller particle size has more defects which are due to physical grinding.
基金The project supported by the National Natural Science Foundation of China(10032010,10372004)Shanghai Leading Academic Discipline
文摘Classical micromechanical methods for calculating the effective moduli of a heteroge- neous material are generalized to include the interface(surface)effect.By using Hashin's Composite Sphere Assemblage(CSA)model,a new expression of the bulk modulus for a particle-reinforced com- posite is derived.It is emphasized that the present study is within the finite-deformation framework such that the effective properties are not influenced by the interface stress itself solely,but influenced by the change of the interface stress due to changes of the shape and size of the interface.Hence some inadequacies in previous papers are pointed out.
基金supported by the National Natural Science Foundation of China (Nos. 21227802, 21303216 and 21473217)
文摘The salt effects on molecular orientation at air/liquid methanol interface were investigated by the polarization-dependent sum frequency generation vibrational spectroscopy（SFG-VS）. We clarified that the average tilting angle of the methyl group to be u = 308 58 at the air/pure methanol surface assuming a d-function orientational distribution. Upon the addition of 3 mol/L Na I, the methyl group tilts further away from the surface normal with a new u = 418 38. This orientational change does not explain the enhancement of the SFG-VS intensities when adding Na I, implying the number density of the methanol molecules with a net polar ordering in the surface region also changed with the Na I concentrations. These spectroscopic findings shed new light on the salt effects on the surfaces structures of the polar organic solutions. It was also shown that the accurate determination of the bulk refractive indices and Raman depolarization ratios for different salt concentrations is crucial to quantitatively interpret the SFG-VS data.
基金Project supported by the National Natural Science Foundation of China(Grant Nos.61376096,61327813,and 11234007)
文摘The dependences of Fermi-level pinning on interface state densities for the metal-dielectric, ploycrystalline silicon-dielectric, and metal silicide-dielectric interfaces are investigated by calculating their effective work functions and their pinning factors. The Fermi-level pinning factors and effective work functions of the metal-dielectric interface are observed to be more susceptible to the increasing interface state densities, differing significantly from that of the ploycrystalline silicon-dielectric interface and the metal silicide-dielectric interface. The calculation results indicate that metal silicide gates with high-temperature resistance and low resistivity are a more promising choice for the design of gate materials in metal-oxide semiconductor（MOS） technology.
基金supported by National Natural Science Foundation of China (21705036, 21975067, 11974105, and 11634001)National Basic Research Programs of China (2016YFA0300901)+3 种基金Natural Science Foundation of Hunan Province, China (2018JJ3035)Fundamental Research Funds for the Central Universities from Hunan Universityfinancially supported by the fund of Prof. Hong from University of Macao (SRG201600092-IAPME, MYRG2018-00079-IAPME, MYRG2019-00115-IAPME)the Science and Technology Development Fund, Macao SAR (FDCT081/2017/A2, FDCT0059/2018/A2, FDCT009/2017/AMJ)
文摘The catalytic performance of Molybdenum disulfide(MoS_(2)) has been still far from that of Pt-based catalysts for inadequate active sites and sluggish electron transfer kinetics. Through engineering the interface between MoS_(2)-based materials and supported substrates, hybrid Ru-doped MoS_(2) on carbonized lignin(CL) is designed and prepared as efficient catalyst for hydrogen evolution reaction(HER). The CL substrate not only facilitates the growth of MoS_(2) nanoflowers, but also promotes the electron transfer. Ru doping increases active sites greatly for HER. The hybrid catalyst achieves a low onset overpotential of 25 mV and a low Tafel slope of 46 m V dec^(-1). The favorable HER activity ascribes to the interfacial interaction between MoS_(2) and CL. Density functional theory calculations further confirm the improved HER performance with doped Ru atoms. This study presents a prototype application to design electrocatalysts with enhanced carrier mobility and high-density active sites based on interface effect.
