Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible s...Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.展开更多
The application of conventional manganese dioxide(MnO_(2))materials in sodium-ion supercapacitors(Na-SCs)is considerably limited by their low conductivity and structural instability.Biomimetic morphology engineering c...The application of conventional manganese dioxide(MnO_(2))materials in sodium-ion supercapacitors(Na-SCs)is considerably limited by their low conductivity and structural instability.Biomimetic morphology engineering can optimize the electrochemical performance of MnO_(2).Here,based on the metal-organic frameworks(MOFs)-derived method and electrochemical reconstruction,a coral-like MnO_(2)structure integrated with a functional nitrogen-doped carbon(NC)coating is designed for Na-SC application.The bioinspired coral-like structure captures numerous electrolyte ions and increases the Na+concentration on the electrode surface,which is beneficial for optimizing the Na+transport pathway and accelerating the electrode reaction kinetics.Moreover,the coral-like crosslinked structure effectively enhances the mechanical properties,enabling the maintenance of the structure of MnO_(2)-based electrodes during long-term operation.Furthermore,in/ex-situ characterizations are performed to elucidate the mechanism of lattice transformation during electrochemical phase reconstruction.Additionally,the theoretical calculation and simulation results reveal the ion/electron dynamics in the fabricated electrode.The prepared electrode demonstrates excellent capacitance storage ability(340.7 F g^(−1)at 0.5 A g^(−1))and cycling stability(85.1%capacitance retention after 10,000 cycles).The assembled hybrid device exhibits exceptional life-span(82.0%capacitance retention after 10,000 cycles)and exceptional energy density(36.5 Wh kg^(−1)).This study provides a reliable biomimetic morphology design strategy for MnO_(2)cathodes,paving the way for the fabrication of high-performance Na-SCs.展开更多
Transportation structures such as composite pavements and railway foundations typically consist of multi-layered media designed to withstand high bearing capacity.A theoretical understanding of load transfer mechanism...Transportation structures such as composite pavements and railway foundations typically consist of multi-layered media designed to withstand high bearing capacity.A theoretical understanding of load transfer mechanisms in these multi-layer composites is essential,as it offers intuitive insights into parametric influences and facilitates enhanced structural performance.This paper employs an improved transfer matrix method to address the limitations of existing theoretical approaches for analyzing multi-layer composite structures.By establishing a twodimensional composite pavement model,it investigates load transfer characteristics and validates the accuracy through finite element simulation.The proposed method offers a straightforward analytical approach for examining internal interactions between structural layers.Case studies indicate that the concrete surface layer is the main load-bearing layer for most vertical normal and shear stresses.The soil base layer reduces the overall mechanical response of the substructure,while horizontal actions increase the risk of interfacial slip and cracking.Structural optimization analysis demonstrates that increasing the thickness of the concrete surface layer,enhancing the thickness and stiffness of the soil base layer,or incorporating gradient layers can significantly mitigate these risks of interfacial slip and cracking.The findings of this study can guide the optimization design,parameter analysis,and damage prevention of multi-layer composite structures.展开更多
Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to conce...Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to concentration quenching has become a key research focus.In this work,we successfully synthesized KBi(MoO_(4))_(2):x Tb^(3+)(x=0-100 at%)(denoted as KBM:x Tb^(3+))phosphors via a high-temperature solid-state reaction.Remarkably,no concentration quenching was observed across the entire doping range.This anti-quenching behavior originates from the large Tb^(3+)-Tb^(3+)interionic distance(>5Å)inherent to the quasi-layered crystal structure,which effectively suppresses multipole-interaction-mediated energy migration.At full Tb^(3+)substitution(x=100 at%),the material undergoes a structural phase transition from the monoclinic KBM phase to the triclinicα-KTb(MoO_(4))_(2)(α-KTM)phase.Theα-KTM phosphor exhibits excellent thermal stability(activation energy=0.6129 eV)and a single-exponential decay profile,whereas KBM:x Tb^(3+)(x<100%)display double-exponential decay behaviors,attributed to dual energy transfer pathways.These findings provide new insights into the luminescence mechanisms of high-concentration rare-earth-doped systems and offer guidance for designing nextgeneration anti-quenching phosphors.展开更多
Understanding the evolution of microstructures in nuclear fuels under high-burn-up conditions is critical for extending fuel refueling cycles and enhancing nuclear reactor safety.In this study,a phase-field model is p...Understanding the evolution of microstructures in nuclear fuels under high-burn-up conditions is critical for extending fuel refueling cycles and enhancing nuclear reactor safety.In this study,a phase-field model is proposed to examine the evolution of high-burn-up structures in polycrystalline UO_(2).The formation and growth of recrystallized grains were initially investigated.It was demonstrated that recrystallization kinetics adhere to the Kolmogorov–Johnson–Mehl–Avrami(KJMA)equation,and that recrystallization represents a process of free-energy reduction.Subsequently,the microstructural evolution in UO_(2) was analyzed as the burn up increased.Gas bubbles acted as additional nucleation sites,thereby augmenting the recrystallization kinetics,whereas the presence of recrystallized grains accelerated bubble growth by increasing the number of grain boundaries.The observed variations in the recrystallization kinetics and porosity with burn-up closely align with experimental findings.Furthermore,the influence of grain size on microstructure evolution was investigated.Larger grain sizes were found to decrease porosity and the occurrence of high-burn-up structures.展开更多
The toughness of thermoplastic polymers such as polypropylene(PP)can be improved by adding elastomers-based toughening agents,and the phase morphology of these toughening agents is very important for the strength and ...The toughness of thermoplastic polymers such as polypropylene(PP)can be improved by adding elastomers-based toughening agents,and the phase morphology of these toughening agents is very important for the strength and toughness of PP.The low-temperature toughness of PP was improved by inserting high-density polyethylene(HDPE)between PP and polystyrene-b-ethylene-co-propyleneb-polystyrene(SEPS)to form an unusual SEPS@HDPE core–shell structure,with SEPS as the core and HDPE as the shell.Based on the microtopography and rheological behavior characterization,HDPE in PP/SEPS/HDPE composites was found to serve as an emulsifier,decrease the size of SEPS particles,and promote the homogeneous dispersion of dispersed phase particles in the matrix.An increase in the HDPE content shifted the toughening mechanism of PP composites from cavitation to matrix shear yielding.The reduction in the distance between the dispersed core–shell structure particles promoted shear yielding in the PP composites,leading to increased toughness.The creation of an intermediate HDPE layer with a moderate modulus was crucial for dispersing stress concentrations and significantly improving toughness without compromising the tensile strength.These findings will facilitate the fabrication of high-toughness PP products at low temperatures.展开更多
With the continuously increasing awareness of energy conservation and the intensifying impacts of global warming, Personal Thermal Management (PTM) technologies are increasingly recognized for their potential to ensur...With the continuously increasing awareness of energy conservation and the intensifying impacts of global warming, Personal Thermal Management (PTM) technologies are increasingly recognized for their potential to ensure human thermal comfort in extreme environments. Biomimetic structures have emerged as a novel source of inspiration for PTM applications. This review systematically summarizes the biomimetic structures, phase change materials, manufacturing methods, and the performance of multifunctional PTM wearables. Firstly, it analyzes the biomimetic structures with thermal regulation and encapsulated phase change material functionalities from different dimensions, highlighting their applications in PTM. Subsequently, it outlines the conventional manufacturing methods incorporating various biomimetic structures, offering strategies for the production of PTM wearables. The review also discusses the typical performance characteristics of multifunctional PTM wearables, addressing the current demands in thermal management. Finally, opportunities and challenges in PTM field are proposed, proposing new directions for future research.展开更多
LiFePO_(4)has normal olivine-structured(a-LFP)and high pressure(b-LFP)phases,with the former being one of the cathode materials for commercial Li-ion batteries.Despite extensive focus on the respective electrochemical...LiFePO_(4)has normal olivine-structured(a-LFP)and high pressure(b-LFP)phases,with the former being one of the cathode materials for commercial Li-ion batteries.Despite extensive focus on the respective electrochemical properties of the two phases,there is a lack of comparative studies on their electronic and magnetic properties,and the origin of the structural phase transition remains unclear.By combining first-principles calculations with molecular dynamics simulations,we find that the anisotropic compression of Li-O bonds drives the structural phase transition from a-LFP to b-LFP at a critical pressure of 20 GPa,while b-LFP undergoes a transition from semiconductor to metal due to Fe^(3+)generated during delithiation.Their antiferromagnetic(AFM)ground states are predicted to arise from the negative magnetic exchange interactions between nearest and next-nearest neighbor sites,with the corresponding N'eel temperature showing significant enhancement under pressure.Furthermore,compared with a-LFP,b-LFP shows increases in bulk,shear,and Young’s moduli of 8%,13%,and 12%,respectively.These findings enrich the physical property data of LiFePO_(4)phase compounds,providing knowledge for expanding the application scenarios of the a-LFP phase under special operating conditions such as high pressure.展开更多
Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the...Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the cathode side,which strictly requires the development of high voltage,high capacity,and earth-abundant cathode material.Ni-Fe-Mn ternary layered oxide has been recognized as one of the most promising standard type of cathodes.However,the composition and phase structure on high-voltage characteristics have not been well investigated.Herein,selecting the typically high-voltage cathode of P2-Na_(0.67)Ni_(0.33)Mn_(0.67)O_(2)as a parent material,we fabricate ten Ni-Fe-Mn ternary layered oxides through replacing the Ni,Mn,or both Ni and Mn by Fe.The thermodynamically stable phase diagram for those materials is presented.The electrochemical properties for all the samples are investigated in detail.Three potential Ni-Fe-Mn ternary layered oxides are picked up considering the energy density,cycle stability,kinetics,cost price,and working voltage,which demonstrate great potential for surpassing the performance of lithium iron phosphate.The related electrochemical reaction and fading mechanism are well revealed.This work provides some new foundational Ni-Fe-Mn ternary layered materials for high-voltage sodium-ion batteries.展开更多
The recovery and utilization of ubiquitous low-grade heat are crucial for mitigating the fossil energy crisis.However,uncontrolled spontaneous heat dissipation limits its practical application.Inspired by skeletal mus...The recovery and utilization of ubiquitous low-grade heat are crucial for mitigating the fossil energy crisis.However,uncontrolled spontaneous heat dissipation limits its practical application.Inspired by skeletal muscle thermogenesis,we develop a compressible wood phase change gel with mechano-controlled heat release by infiltrating xylitol gel into wood aerogel.The xylitol gel can store recovered low-grade heat for at least 1 month by leveraging its inherent energy barrier.The hierarchically aligned lamellar structure of wood aerogel facilitates mechanical adaptation,hydrogen bond formation,and energy dissipation between the wood aerogel and the xylitol gel,increasing the compressive strength and toughness of wood phase change gel fivefold compared to xylitol gel.This enhancement effect enables repetitive contact-separation motions between the wood phase change gel and the substrate during radial compression,overcoming the energy barrier and releasing approximately 178.6 J g−1 of heat.As a proof-of-concept,the wood phase change gel serves as the hot side in a thermoelectric generator,providing about 2.13 W m^(−2) of clean electricity by the controlled utilization of recovered solar heat.This study presents a sustainable method to achieve off-grid electricity generation through the controlled utilization of recovered low-grade heat.展开更多
A two-dimensional electromagnetic particle-in-cell simulation model is proposed to study the density evolution and collective stopping of electron beams in background plasmas.We show here the formation of the multi-la...A two-dimensional electromagnetic particle-in-cell simulation model is proposed to study the density evolution and collective stopping of electron beams in background plasmas.We show here the formation of the multi-layer structure of the relativistic electron beam in the plasma due to the different betatron frequency from the beam front to the beam tail.Meanwhile,the nonuniformity of the longitudinal wakefield is the essential reason for the multi-layer structure formation in beam phase space.The influences of beam parameters(beam radius and transverse density profile)on the formation of the multi-layer structure and collective stopping in background plasmas are also considered.展开更多
With the continuous improvement of China's science and technology, the design method of steel structure is also more and more, how to better apply the module building design method to the related buildings, is the...With the continuous improvement of China's science and technology, the design method of steel structure is also more and more, how to better apply the module building design method to the related buildings, is the current issue to focus on consideration. Therefore, this paper will focus on the design method of multi-layer steel structure module and steel frame composite building structure, and analyze and study its structure, so as to improve the utilization rate of steel structure and promote the development of the construction industry.展开更多
La0.7Ce0.3Ni3.75Mn0.35Al0.15Cu0.75-xFex （x=0-0.20） hydrogen storage alloys were synthesized by induction melting and subsequent annealing treatment, and phase structure and electrochemical characteristics were inves...La0.7Ce0.3Ni3.75Mn0.35Al0.15Cu0.75-xFex （x=0-0.20） hydrogen storage alloys were synthesized by induction melting and subsequent annealing treatment, and phase structure and electrochemical characteristics were investigated. All alloys consist of a single LaNi5 phase with CaCu5 structure, and the lattice constant a and the cell volume （V） of the LaNi5 phase increase with increasing x value. The maximum discharge capacity gradually decreases from 319.0 mA？h/g （x=0） to 291.9 mA？h/g （x=0.20） with the increase in x value. The high-rate dischargeability at the discharge current density of 1200 mA/g decreases monotonically from 53.1% （x=0） to 44.2% （x=0.20）. The cycling stability increases with increasing x from 0 to 0.20, which is mainly ascribed to the improvement of the pulverization resistance.展开更多
The microstructure and phase composition of as-cast Mg-9Er-6Y-xZn-0.6Zr （x=1, 2, 3, 4; normal mass fraction in %） alloys were investigated. In low Zn content, aside from the major second phase of Mg24（Er, Y, Zn）5,...The microstructure and phase composition of as-cast Mg-9Er-6Y-xZn-0.6Zr （x=1, 2, 3, 4; normal mass fraction in %） alloys were investigated. In low Zn content, aside from the major second phase of Mg24（Er, Y, Zn）5, there are a few lamellar phases that grow parallel with each other from the grain boundaries to the grain interior. With Zn content increasing, the Mg24（Er, Y, Zn）5 phase decreases, but the Mg12Zn（Y, Er） phase and lamellar phases continuously increase. When Zn content reaches 4% （normal mass fraction）, the Mg12Zn（Y, Er） phase mainly exists as large bulks, and some a-Mg grains are thoroughly penetrated by the lamellar phases. Moreover, the crystallography structures of the Mgl2Zn（Y, Er） and Mg24（Er, Y, Zn）5 phases are confirmed as 18R-type long-period stacking ordered structure and body-centred cubic structure, respectively.展开更多
To improve the electrochemical properties of rare-earth-Mg-Ni-based hydrogen storage alloys, the effects of stoichiometry and Cu-substitution on the phase structure and thermodynamic properties of the alloys were stud...To improve the electrochemical properties of rare-earth-Mg-Ni-based hydrogen storage alloys, the effects of stoichiometry and Cu-substitution on the phase structure and thermodynamic properties of the alloys were studied. Nonsubstituted Ml0.80Mg0.20（Ni2.90Co0.50-Mn0.30Al0.30）x （x=0.68, 0.70, 0.72, 0.74, 0.76） alloys and Cu-substituted Ml0.80Mg0.20（Ni2.90Co0.50-yCuyMn0.30Al0.30）0.70 （y=0, 0.10, 0.30, 0.50） alloys were prepared by induction melting. Phase structure analysis shows that the nonsubstituted alloys consist of a LaNi5 phase, a LaNi3 phase, and a minor La2Ni7 phase;in addition, in the case of Cu-substitution, the Nd2Ni7 phase appears and the LaNi3 phase vanishes. Ther-modynamic tests show that the enthalpy change in the dehydriding process decreases, indicating that hydride stability decreases with in-creasing stoichiometry and increasing Cu content. The maximum discharge capacity, kinetic properties, and cycling stability of the alloy electrodes all increase and then decrease with increasing stoichiometry or increasing Cu content. Furthermore, Cu substitution for Co ame-liorates the discharge capacity, kinetics, and cycling stability of the alloy electrodes.展开更多
The effects of the partial replacement of Co with Mo on the phase structure and electrochemical kinetic properties of La0.35Ce0.65Ni3.54Co0.80-xMn0.35Al0.32Mox （x=0.00, 0.10, 0.15, 0.20, 0.25） hydrogen storage alloy...The effects of the partial replacement of Co with Mo on the phase structure and electrochemical kinetic properties of La0.35Ce0.65Ni3.54Co0.80-xMn0.35Al0.32Mox （x=0.00, 0.10, 0.15, 0.20, 0.25） hydrogen storage alloys prepared by arc-melting method were sys-tematically studied in this paper. The X-ray diffraction （XRD） showed that after partial substitution of Mo for Co, the alloys remained a single LaNi5 phase with a hexagonal CaCu5-type structure. The P-C isotherms indicated that the equilibrium pressure gradually decreased with in-creasing of Mo content. Electrochemical studies showed that the substitution of Mo for Co could greatly increase discharge capacity, improve activation ability and reduce self-discharge of alloy electrodes. The alloy with x=0.25 exhibited a higher rate dischargeability （HRD1200= 50.9%）. Moreover, Mo is a vital element in favor of kinetic properties of AB5-type hydrogen storage alloys. As Mo content increased, the ex-change current density I0, the hydrogen diffusion rate gradually increased.展开更多
In this communication, the crystal structure of Cr_4AlB_4, a new MAB phase compound(where M is a transition metal, A is Al or Si, B is boron) discovered in Cr-Al-B system is reported. This new MAB phase was synthesize...In this communication, the crystal structure of Cr_4AlB_4, a new MAB phase compound(where M is a transition metal, A is Al or Si, B is boron) discovered in Cr-Al-B system is reported. This new MAB phase was synthesized from a mixture of CrB and Al powders at 1000?C and its crystal structure was determined by a combination of X-ray diffraction, first-principles calculations and energy dispersive X-ray spectroscopy(EDS). Cr_4AlB_4 crystallizes in an orthorhombic structure with Immm space group. The lattice constants are a = 2.9343(6) ?, b = 18.8911(0) ?, c = 2.9733(7) ?, and the atomic positions are Cr1 at 4 g(0, 0.2936(5),0), Cr2 at 4 h(0.5, 0.5859(7), 0), Al at 2 b(0, 0.5, 0.5), B1 at 4 h(0, 0.3839(8), 0.5) and B2 at 4 g(0.5, 0.6646(2),0.5).展开更多
Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bon...Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bonding temperature of 1273K Ni reacts with SiC and forms various Ni silicides con- taining graphite baside SiC. Ni3Si without graphite was formed at Ni side.The interface structure of SiC/Ni joint was SiC/Ni2Si + C/Ni31 Si12 + G/Ni3 Si/Ni. At the interface between SiC and Ni- 25at%Cr alloy the Ni silicide was only Ni2Si at the same bonding temperature,and further(Cr, Ni)7 (Si, C)3 carbide was formed between Ni silicide + graphite zone and Ni - 25at%Cr alloy.The interface structure of SiC/Ni - 25at%Cr alloy was SiC/Ni2Si + C/(Cr, Ni)7 (Si, C)3+Ni(ss. Cr, Si)/Ni - 25at%Cr.展开更多
The phase stability,elastic properties and electronic structures of three typical Mg-Y intermetallics including Mg_(24)Y_(5),Mg_(2)Y and MgY are systematically investigated using first-principles calculations based on...The phase stability,elastic properties and electronic structures of three typical Mg-Y intermetallics including Mg_(24)Y_(5),Mg_(2)Y and MgY are systematically investigated using first-principles calculations based on density functional theory.The optimized structural parameters including lattice constants and atomic coordinates are in good agreement with experimental values.The calculated cohesive energies and formation enthalpies show that either phase stability or alloying ability of the three intermetallics is gradually enhanced with increasing Y content.The single-crystal elastic constants C_(ij) of Mg-Y intermetallics are also calculated,and the bulk modulus B,shear modulus G,Young's modulus E,Poisson ratio v and anisotropy factor A of polycrystalline materials are derived.It is suggested that the resistances to volume and shear deformation as well as the stiffness of the three intermetallics are raised with increasing Y content.Besides,these intermetallics all exhibit ductile characteristics,and they are isotropic in compression but anisotropic to a certain degree in shear and stiffness.Comparatively,Mg_(24)Y_(5) presents a relatively higher ductility,while MgY has a relatively stronger anisotropy in shear and stiffness.Further analysis of electronic structures indicates that the phase stability of Mg-Y intermetallics is closely related with their bonding electrons numbers below Fermi level.Namely,the more bonding electrons number below Fermi level corresponds to the higher structural stability of Mg-Y intermetallics.展开更多
Microporous membranes of low-high density polyethylene and their blends were prepared bythermally-induced phase separation of polymer/long-aliphatic chain alcohol (diluent) mixtures.The microstructures of this particu...Microporous membranes of low-high density polyethylene and their blends were prepared bythermally-induced phase separation of polymer/long-aliphatic chain alcohol (diluent) mixtures.The microstructures of this particular membrane, which depends on the diluent properties,polymer concentration and cooling rate, were observed by scanning electron microscopy.'Beehive-type,'leafy-like, and lacy porous structure morphologies can be formed,depending onthe blend composition and phase separation conditions, which were discussed by the polymer anddiluent crystallization processes.展开更多
基金financially supported by the supported by Shandong Provincial Natural Science Foundation(ZR2024MB108)Taishan Young Scholar Program(tsqn202312312)Excellent Young Scholars of the Shandong Provincial Natural Science Foundation(Overseas)(2023HWYQ-112)。
文摘Conversion-type electrode materials hold significant promise for potassium-ion batteries(PIBs)due to their high theoretical capacities,yet their practical deployment is hindered by sluggish kinetics and irreversible structural degradation.To overcome these limitations,we propose a rationally engineered nanoreactor architecture that stabilizes defect-rich MoS_(2)via interlayer incorporation of a carbon monolayer,followed by encapsulation within a nitrogen-doped carbon shell,forming a MoSSe@NC heterostructure.This tailored structure synergistically accelerates both K^(+)diffusion kinetics and electron transfer,enabling unprecedented rate performance(107 mAh g^(-1)at 10 Ag^(-1))and ultralong cyclability(86.5%capacity retention after 1200 cycles at 3 A g^(-1)).Mechanistic insights reveal a distinctive“adsorption-conversion”pathway,where sulfur vacancies on exposed S-Mo-S basal planes act as preferential K^(+)adsorption sites,effectively suppressing parasitic phase transitions during intercalation.In situ X-ray diffraction and transmission electron microscopy corroborate the structural reversibility of the conversion reaction,with the carbon matrix dynamically accommodating strain while preserving electrode integrity.This work not only advances the understanding of defect-driven interfacial chemistry in conversion-type materials but also provides a versatile strategy for designing high-performance anodes in next-generation PIBs through heterostructure engineering.
基金supported by the National Natural Science Foundation of China(22409065)the Guangdong Basic and Applied Basic Research Foundation(2022A1515011906)+2 种基金the China Postdoctoral Science Foundation(2023M731153)the Research Fund Program of Guangdong Provincial Key Laboratory of Fuel Cell Technologythe Postdoctoral Fellowship Program of CPSF(GZC20230868).
文摘The application of conventional manganese dioxide(MnO_(2))materials in sodium-ion supercapacitors(Na-SCs)is considerably limited by their low conductivity and structural instability.Biomimetic morphology engineering can optimize the electrochemical performance of MnO_(2).Here,based on the metal-organic frameworks(MOFs)-derived method and electrochemical reconstruction,a coral-like MnO_(2)structure integrated with a functional nitrogen-doped carbon(NC)coating is designed for Na-SC application.The bioinspired coral-like structure captures numerous electrolyte ions and increases the Na+concentration on the electrode surface,which is beneficial for optimizing the Na+transport pathway and accelerating the electrode reaction kinetics.Moreover,the coral-like crosslinked structure effectively enhances the mechanical properties,enabling the maintenance of the structure of MnO_(2)-based electrodes during long-term operation.Furthermore,in/ex-situ characterizations are performed to elucidate the mechanism of lattice transformation during electrochemical phase reconstruction.Additionally,the theoretical calculation and simulation results reveal the ion/electron dynamics in the fabricated electrode.The prepared electrode demonstrates excellent capacitance storage ability(340.7 F g^(−1)at 0.5 A g^(−1))and cycling stability(85.1%capacitance retention after 10,000 cycles).The assembled hybrid device exhibits exceptional life-span(82.0%capacitance retention after 10,000 cycles)and exceptional energy density(36.5 Wh kg^(−1)).This study provides a reliable biomimetic morphology design strategy for MnO_(2)cathodes,paving the way for the fabrication of high-performance Na-SCs.
基金supported by Fundamental Research Funds for the Central Universities(No.lzujbky-2024-05)Innovation Foundation of Provincial Education Department of Gansu(2024B-005)+2 种基金Scientific Department of Gansu(24CXGA083,24CXGA024,JK2024-28,JK2024-32 and 23CXJA0007)Industrial Support Plan Project of Provincial Education Department of Gansu(2025CYZC-003 and CYZC-2024-10)the Hunan Natural Science Foundation Science and Education Joint Fund Project(2022JJ60109).
文摘Transportation structures such as composite pavements and railway foundations typically consist of multi-layered media designed to withstand high bearing capacity.A theoretical understanding of load transfer mechanisms in these multi-layer composites is essential,as it offers intuitive insights into parametric influences and facilitates enhanced structural performance.This paper employs an improved transfer matrix method to address the limitations of existing theoretical approaches for analyzing multi-layer composite structures.By establishing a twodimensional composite pavement model,it investigates load transfer characteristics and validates the accuracy through finite element simulation.The proposed method offers a straightforward analytical approach for examining internal interactions between structural layers.Case studies indicate that the concrete surface layer is the main load-bearing layer for most vertical normal and shear stresses.The soil base layer reduces the overall mechanical response of the substructure,while horizontal actions increase the risk of interfacial slip and cracking.Structural optimization analysis demonstrates that increasing the thickness of the concrete surface layer,enhancing the thickness and stiffness of the soil base layer,or incorporating gradient layers can significantly mitigate these risks of interfacial slip and cracking.The findings of this study can guide the optimization design,parameter analysis,and damage prevention of multi-layer composite structures.
基金supported by the Natural Science Research Project of Anhui Province Education Department for Excellent Young Scholars(Grant No.2024AH030007)the National Natural Science Foundation of China(Grant No.52202001)。
文摘Conventional Tb^(3+)-doped phosphors typically suffer from concentration quenching once the doping level exceeds a critical threshold.Consequently,the development of Tb^(3+)phosphors with intrinsic resistance to concentration quenching has become a key research focus.In this work,we successfully synthesized KBi(MoO_(4))_(2):x Tb^(3+)(x=0-100 at%)(denoted as KBM:x Tb^(3+))phosphors via a high-temperature solid-state reaction.Remarkably,no concentration quenching was observed across the entire doping range.This anti-quenching behavior originates from the large Tb^(3+)-Tb^(3+)interionic distance(>5Å)inherent to the quasi-layered crystal structure,which effectively suppresses multipole-interaction-mediated energy migration.At full Tb^(3+)substitution(x=100 at%),the material undergoes a structural phase transition from the monoclinic KBM phase to the triclinicα-KTb(MoO_(4))_(2)(α-KTM)phase.Theα-KTM phosphor exhibits excellent thermal stability(activation energy=0.6129 eV)and a single-exponential decay profile,whereas KBM:x Tb^(3+)(x<100%)display double-exponential decay behaviors,attributed to dual energy transfer pathways.These findings provide new insights into the luminescence mechanisms of high-concentration rare-earth-doped systems and offer guidance for designing nextgeneration anti-quenching phosphors.
基金supported by the National Natural Science Foundation of China(Grant Nos.U20B2013 and 12205286)the National Key Research and Development Program of China(Grant No.2022YFB1902401)。
文摘Understanding the evolution of microstructures in nuclear fuels under high-burn-up conditions is critical for extending fuel refueling cycles and enhancing nuclear reactor safety.In this study,a phase-field model is proposed to examine the evolution of high-burn-up structures in polycrystalline UO_(2).The formation and growth of recrystallized grains were initially investigated.It was demonstrated that recrystallization kinetics adhere to the Kolmogorov–Johnson–Mehl–Avrami(KJMA)equation,and that recrystallization represents a process of free-energy reduction.Subsequently,the microstructural evolution in UO_(2) was analyzed as the burn up increased.Gas bubbles acted as additional nucleation sites,thereby augmenting the recrystallization kinetics,whereas the presence of recrystallized grains accelerated bubble growth by increasing the number of grain boundaries.The observed variations in the recrystallization kinetics and porosity with burn-up closely align with experimental findings.Furthermore,the influence of grain size on microstructure evolution was investigated.Larger grain sizes were found to decrease porosity and the occurrence of high-burn-up structures.
基金supported by the Taiyuan Major Science and Technology Project Fund in 2021,Fund for Shanxi“1331 Project,”Key Research and Development Program of Shanxi Province(202102040201011)the Zhanjiang Marine Equipment and Marine Biological Industry Unveiled the Talent Team Project(2021E05034).
文摘The toughness of thermoplastic polymers such as polypropylene(PP)can be improved by adding elastomers-based toughening agents,and the phase morphology of these toughening agents is very important for the strength and toughness of PP.The low-temperature toughness of PP was improved by inserting high-density polyethylene(HDPE)between PP and polystyrene-b-ethylene-co-propyleneb-polystyrene(SEPS)to form an unusual SEPS@HDPE core–shell structure,with SEPS as the core and HDPE as the shell.Based on the microtopography and rheological behavior characterization,HDPE in PP/SEPS/HDPE composites was found to serve as an emulsifier,decrease the size of SEPS particles,and promote the homogeneous dispersion of dispersed phase particles in the matrix.An increase in the HDPE content shifted the toughening mechanism of PP composites from cavitation to matrix shear yielding.The reduction in the distance between the dispersed core–shell structure particles promoted shear yielding in the PP composites,leading to increased toughness.The creation of an intermediate HDPE layer with a moderate modulus was crucial for dispersing stress concentrations and significantly improving toughness without compromising the tensile strength.These findings will facilitate the fabrication of high-toughness PP products at low temperatures.
基金supported by Basic and Applied Basic Research Foundation of Guangdong Province(No.2024A1515010772)State Key Laboratory of Massive Personalized Customization System and Technology,No.H&C-MPC-2023-02-06(Q)+2 种基金“CUG scholar”Scientific Research Funds at China University of Geosciences,Wuhan(No.CUG2022185)Guangzhou Youth Top Talent ProgramChina College Student Innovation and Entrepreneurship Training Program(No.S202410491063).
文摘With the continuously increasing awareness of energy conservation and the intensifying impacts of global warming, Personal Thermal Management (PTM) technologies are increasingly recognized for their potential to ensure human thermal comfort in extreme environments. Biomimetic structures have emerged as a novel source of inspiration for PTM applications. This review systematically summarizes the biomimetic structures, phase change materials, manufacturing methods, and the performance of multifunctional PTM wearables. Firstly, it analyzes the biomimetic structures with thermal regulation and encapsulated phase change material functionalities from different dimensions, highlighting their applications in PTM. Subsequently, it outlines the conventional manufacturing methods incorporating various biomimetic structures, offering strategies for the production of PTM wearables. The review also discusses the typical performance characteristics of multifunctional PTM wearables, addressing the current demands in thermal management. Finally, opportunities and challenges in PTM field are proposed, proposing new directions for future research.
基金supported by the National Natural Science Foundation of China(Grant No.12304089)the start-up foundation from Shanghai University。
文摘LiFePO_(4)has normal olivine-structured(a-LFP)and high pressure(b-LFP)phases,with the former being one of the cathode materials for commercial Li-ion batteries.Despite extensive focus on the respective electrochemical properties of the two phases,there is a lack of comparative studies on their electronic and magnetic properties,and the origin of the structural phase transition remains unclear.By combining first-principles calculations with molecular dynamics simulations,we find that the anisotropic compression of Li-O bonds drives the structural phase transition from a-LFP to b-LFP at a critical pressure of 20 GPa,while b-LFP undergoes a transition from semiconductor to metal due to Fe^(3+)generated during delithiation.Their antiferromagnetic(AFM)ground states are predicted to arise from the negative magnetic exchange interactions between nearest and next-nearest neighbor sites,with the corresponding N'eel temperature showing significant enhancement under pressure.Furthermore,compared with a-LFP,b-LFP shows increases in bulk,shear,and Young’s moduli of 8%,13%,and 12%,respectively.These findings enrich the physical property data of LiFePO_(4)phase compounds,providing knowledge for expanding the application scenarios of the a-LFP phase under special operating conditions such as high pressure.
基金financially supported by the National Natural Science Foundation of China(Grant No.52402215)the Anhui Provincial Natural Science Foundation(2408085QB036)+1 种基金the Natural Science Research Project of Anhui Province Education Department(Grant Nos.2022AH050334,2022AH030046,2023AH051119)the Scientific Research Foundation of Anhui University of Technology for Talent Introduction(DT2200001211)。
文摘Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the cathode side,which strictly requires the development of high voltage,high capacity,and earth-abundant cathode material.Ni-Fe-Mn ternary layered oxide has been recognized as one of the most promising standard type of cathodes.However,the composition and phase structure on high-voltage characteristics have not been well investigated.Herein,selecting the typically high-voltage cathode of P2-Na_(0.67)Ni_(0.33)Mn_(0.67)O_(2)as a parent material,we fabricate ten Ni-Fe-Mn ternary layered oxides through replacing the Ni,Mn,or both Ni and Mn by Fe.The thermodynamically stable phase diagram for those materials is presented.The electrochemical properties for all the samples are investigated in detail.Three potential Ni-Fe-Mn ternary layered oxides are picked up considering the energy density,cycle stability,kinetics,cost price,and working voltage,which demonstrate great potential for surpassing the performance of lithium iron phosphate.The related electrochemical reaction and fading mechanism are well revealed.This work provides some new foundational Ni-Fe-Mn ternary layered materials for high-voltage sodium-ion batteries.
基金supported by the National Key R&D Program of China (2023YFD2201403)the National Natural Science Foundation of China (Grant Nos. 32171693, 32201482)+1 种基金the Heilongjiang Natural Science Foundation Outstanding Youth project (Grant No. YQ2022C002)College Students'Innovative Entrepreneurial Training Plan Program (202410225338)
文摘The recovery and utilization of ubiquitous low-grade heat are crucial for mitigating the fossil energy crisis.However,uncontrolled spontaneous heat dissipation limits its practical application.Inspired by skeletal muscle thermogenesis,we develop a compressible wood phase change gel with mechano-controlled heat release by infiltrating xylitol gel into wood aerogel.The xylitol gel can store recovered low-grade heat for at least 1 month by leveraging its inherent energy barrier.The hierarchically aligned lamellar structure of wood aerogel facilitates mechanical adaptation,hydrogen bond formation,and energy dissipation between the wood aerogel and the xylitol gel,increasing the compressive strength and toughness of wood phase change gel fivefold compared to xylitol gel.This enhancement effect enables repetitive contact-separation motions between the wood phase change gel and the substrate during radial compression,overcoming the energy barrier and releasing approximately 178.6 J g−1 of heat.As a proof-of-concept,the wood phase change gel serves as the hot side in a thermoelectric generator,providing about 2.13 W m^(−2) of clean electricity by the controlled utilization of recovered solar heat.This study presents a sustainable method to achieve off-grid electricity generation through the controlled utilization of recovered low-grade heat.
基金supported by National Natural Science Foundation of China(Nos.12075046 and 11775042)。
文摘A two-dimensional electromagnetic particle-in-cell simulation model is proposed to study the density evolution and collective stopping of electron beams in background plasmas.We show here the formation of the multi-layer structure of the relativistic electron beam in the plasma due to the different betatron frequency from the beam front to the beam tail.Meanwhile,the nonuniformity of the longitudinal wakefield is the essential reason for the multi-layer structure formation in beam phase space.The influences of beam parameters(beam radius and transverse density profile)on the formation of the multi-layer structure and collective stopping in background plasmas are also considered.
文摘With the continuous improvement of China's science and technology, the design method of steel structure is also more and more, how to better apply the module building design method to the related buildings, is the current issue to focus on consideration. Therefore, this paper will focus on the design method of multi-layer steel structure module and steel frame composite building structure, and analyze and study its structure, so as to improve the utilization rate of steel structure and promote the development of the construction industry.
基金Project (51001043) supported by the National Natural Science Foundation of ChinaProject (NCET2011) supported by Program for New Century Excellent Talents in University, China+4 种基金Project (201104390) supported by China Postdoctoral Science Special FoundationProject (20100470990) supported by China Postdoctoral Science FoundationProject (2012IRTSTHN007) supported by Program for Innovative Research Team (in Science and Technology) in the University of Henan Province, ChinaProject (2011J1003) supported by Baotou Science and Technology Project, ChinaProject (B2010-13) supported by the Doctoral Foundation of Henan Polytechnic University, China
文摘La0.7Ce0.3Ni3.75Mn0.35Al0.15Cu0.75-xFex （x=0-0.20） hydrogen storage alloys were synthesized by induction melting and subsequent annealing treatment, and phase structure and electrochemical characteristics were investigated. All alloys consist of a single LaNi5 phase with CaCu5 structure, and the lattice constant a and the cell volume （V） of the LaNi5 phase increase with increasing x value. The maximum discharge capacity gradually decreases from 319.0 mA？h/g （x=0） to 291.9 mA？h/g （x=0.20） with the increase in x value. The high-rate dischargeability at the discharge current density of 1200 mA/g decreases monotonically from 53.1% （x=0） to 44.2% （x=0.20）. The cycling stability increases with increasing x from 0 to 0.20, which is mainly ascribed to the improvement of the pulverization resistance.
基金Project(NCET-11-0554) supported by the Program for New Century Excellent Talents in University,ChinaProject(2011BAE22B04) supported by the National Key Technology R&D Program,ChinaProject(51271206) supported by the National Natural Science Foundation of China
文摘The microstructure and phase composition of as-cast Mg-9Er-6Y-xZn-0.6Zr （x=1, 2, 3, 4; normal mass fraction in %） alloys were investigated. In low Zn content, aside from the major second phase of Mg24（Er, Y, Zn）5, there are a few lamellar phases that grow parallel with each other from the grain boundaries to the grain interior. With Zn content increasing, the Mg24（Er, Y, Zn）5 phase decreases, but the Mg12Zn（Y, Er） phase and lamellar phases continuously increase. When Zn content reaches 4% （normal mass fraction）, the Mg12Zn（Y, Er） phase mainly exists as large bulks, and some a-Mg grains are thoroughly penetrated by the lamellar phases. Moreover, the crystallography structures of the Mgl2Zn（Y, Er） and Mg24（Er, Y, Zn）5 phases are confirmed as 18R-type long-period stacking ordered structure and body-centred cubic structure, respectively.
基金supported by the National Natural Science Foundation of China(Nos.21303157 and 21106123)the Natural Science Foundation of Hebei Province,China(No.B2012203104)+1 种基金the China Postdoctoral Science Foundation Project(2013M541201)the Research Fund for the Doctoral Program of Higher Education of China(20131333120008)
文摘To improve the electrochemical properties of rare-earth-Mg-Ni-based hydrogen storage alloys, the effects of stoichiometry and Cu-substitution on the phase structure and thermodynamic properties of the alloys were studied. Nonsubstituted Ml0.80Mg0.20（Ni2.90Co0.50-Mn0.30Al0.30）x （x=0.68, 0.70, 0.72, 0.74, 0.76） alloys and Cu-substituted Ml0.80Mg0.20（Ni2.90Co0.50-yCuyMn0.30Al0.30）0.70 （y=0, 0.10, 0.30, 0.50） alloys were prepared by induction melting. Phase structure analysis shows that the nonsubstituted alloys consist of a LaNi5 phase, a LaNi3 phase, and a minor La2Ni7 phase;in addition, in the case of Cu-substitution, the Nd2Ni7 phase appears and the LaNi3 phase vanishes. Ther-modynamic tests show that the enthalpy change in the dehydriding process decreases, indicating that hydride stability decreases with in-creasing stoichiometry and increasing Cu content. The maximum discharge capacity, kinetic properties, and cycling stability of the alloy electrodes all increase and then decrease with increasing stoichiometry or increasing Cu content. Furthermore, Cu substitution for Co ame-liorates the discharge capacity, kinetics, and cycling stability of the alloy electrodes.
基金supported by the National Natural Science Foundation of China (20673093)
文摘The effects of the partial replacement of Co with Mo on the phase structure and electrochemical kinetic properties of La0.35Ce0.65Ni3.54Co0.80-xMn0.35Al0.32Mox （x=0.00, 0.10, 0.15, 0.20, 0.25） hydrogen storage alloys prepared by arc-melting method were sys-tematically studied in this paper. The X-ray diffraction （XRD） showed that after partial substitution of Mo for Co, the alloys remained a single LaNi5 phase with a hexagonal CaCu5-type structure. The P-C isotherms indicated that the equilibrium pressure gradually decreased with in-creasing of Mo content. Electrochemical studies showed that the substitution of Mo for Co could greatly increase discharge capacity, improve activation ability and reduce self-discharge of alloy electrodes. The alloy with x=0.25 exhibited a higher rate dischargeability （HRD1200= 50.9%）. Moreover, Mo is a vital element in favor of kinetic properties of AB5-type hydrogen storage alloys. As Mo content increased, the ex-change current density I0, the hydrogen diffusion rate gradually increased.
基金financial supports from the National Natural Science Foundation of China under grant No.51672064 and No.U1435206
文摘In this communication, the crystal structure of Cr_4AlB_4, a new MAB phase compound(where M is a transition metal, A is Al or Si, B is boron) discovered in Cr-Al-B system is reported. This new MAB phase was synthesized from a mixture of CrB and Al powders at 1000?C and its crystal structure was determined by a combination of X-ray diffraction, first-principles calculations and energy dispersive X-ray spectroscopy(EDS). Cr_4AlB_4 crystallizes in an orthorhombic structure with Immm space group. The lattice constants are a = 2.9343(6) ?, b = 18.8911(0) ?, c = 2.9733(7) ?, and the atomic positions are Cr1 at 4 g(0, 0.2936(5),0), Cr2 at 4 h(0.5, 0.5859(7), 0), Al at 2 b(0, 0.5, 0.5), B1 at 4 h(0, 0.3839(8), 0.5) and B2 at 4 g(0.5, 0.6646(2),0.5).
文摘Bonding of SiC to SiC using Ni and Ni - 25at%Cr foils was performed at high temperature.Interface structures and reaction phases were investigated by EPMA analyses and XRD diffraction method, re- spectively. At a bonding temperature of 1273K Ni reacts with SiC and forms various Ni silicides con- taining graphite baside SiC. Ni3Si without graphite was formed at Ni side.The interface structure of SiC/Ni joint was SiC/Ni2Si + C/Ni31 Si12 + G/Ni3 Si/Ni. At the interface between SiC and Ni- 25at%Cr alloy the Ni silicide was only Ni2Si at the same bonding temperature,and further(Cr, Ni)7 (Si, C)3 carbide was formed between Ni silicide + graphite zone and Ni - 25at%Cr alloy.The interface structure of SiC/Ni - 25at%Cr alloy was SiC/Ni2Si + C/(Cr, Ni)7 (Si, C)3+Ni(ss. Cr, Si)/Ni - 25at%Cr.
基金This work was financially supported by the National Natural Science Foundation of China(No.51401036)the Hunan Provincial Natural Science Foundation of China(No.14JJ3086),the Research Foundation of Education Bureau of Hunan Province(No.12B001)the Key Laboratory of Efficient and Clean Energy Utilization,College of Hunan Province(No.2015NGQ005).
文摘The phase stability,elastic properties and electronic structures of three typical Mg-Y intermetallics including Mg_(24)Y_(5),Mg_(2)Y and MgY are systematically investigated using first-principles calculations based on density functional theory.The optimized structural parameters including lattice constants and atomic coordinates are in good agreement with experimental values.The calculated cohesive energies and formation enthalpies show that either phase stability or alloying ability of the three intermetallics is gradually enhanced with increasing Y content.The single-crystal elastic constants C_(ij) of Mg-Y intermetallics are also calculated,and the bulk modulus B,shear modulus G,Young's modulus E,Poisson ratio v and anisotropy factor A of polycrystalline materials are derived.It is suggested that the resistances to volume and shear deformation as well as the stiffness of the three intermetallics are raised with increasing Y content.Besides,these intermetallics all exhibit ductile characteristics,and they are isotropic in compression but anisotropic to a certain degree in shear and stiffness.Comparatively,Mg_(24)Y_(5) presents a relatively higher ductility,while MgY has a relatively stronger anisotropy in shear and stiffness.Further analysis of electronic structures indicates that the phase stability of Mg-Y intermetallics is closely related with their bonding electrons numbers below Fermi level.Namely,the more bonding electrons number below Fermi level corresponds to the higher structural stability of Mg-Y intermetallics.
文摘Microporous membranes of low-high density polyethylene and their blends were prepared bythermally-induced phase separation of polymer/long-aliphatic chain alcohol (diluent) mixtures.The microstructures of this particular membrane, which depends on the diluent properties,polymer concentration and cooling rate, were observed by scanning electron microscopy.'Beehive-type,'leafy-like, and lacy porous structure morphologies can be formed,depending onthe blend composition and phase separation conditions, which were discussed by the polymer anddiluent crystallization processes.
