High-entropy perovskite ferroelectric materials have attracted significant attention due to their remarkably low remnant polarizations and narrow hysteresis.Thus,these materials offer high-energy density and efficienc...High-entropy perovskite ferroelectric materials have attracted significant attention due to their remarkably low remnant polarizations and narrow hysteresis.Thus,these materials offer high-energy density and efficiency,making them suitable for energy storage applications.Despite significant advancements in experimental research,understanding of the properties associated with structure remains incomplete.This study aims to study the structural,electric,and mechanical performances at various scales of the high-entropy(Na_(0.2)Bi_(0.2)Ca_(0.2)Sr_(0.2)Ba_(0.2))TiO_(3)(NBCSB)material.The results of first-principles calculations indicated that the pseudo-intralayer distortion was obviously smaller compared to the interlayer distortion.Among the various bonds,Bi-O,Ca-O,and Na-O experienced the greatest displacement.Similarly,the hybridization between O 2p and Ti 3d states with Bi 6p states was particularly strong,affecting both the ferroelectric polarization and relaxor behavior.The NBCSB materials produced using a typical solid-state process demonstrated exceptional performance in energy storage with a recoverable density of 1.53 J·cm^(-3)and a high efficiency of 89%when subjected to a small electric field of 120 kV·cm^(-1).In addition,these ceramics displayed a remarkable hardness of around 7.23 GPa.NBCSB ceramics exhibited exceptional relaxation characteristics with minimal hysteresis and low remanent polarization due to its nanoscale high dynamic polarization configuration with diverse symmetries(rhombohedral,tetragonal,and cubic)resulting from randomly dispersed A-site ions.The excellent mechanical property is related to the dislocation-blocking effect,solid solution strengthening effect,and domain boundary effect.The findings of this study offer a comprehensive and novel perspective on A-site disordered high-entropy relaxor ferroelectric ceramics.展开更多
The infamous type Ⅳ failure within the fine-grained heat-affected zone (FGHAZ) in G115 steel weldments seriously threatens the safe operation of ultra-supercritical (USC) power plants.In this work,the traditional the...The infamous type Ⅳ failure within the fine-grained heat-affected zone (FGHAZ) in G115 steel weldments seriously threatens the safe operation of ultra-supercritical (USC) power plants.In this work,the traditional thermo-mechanical treatment was modified via the replacement of hot-rolling with cold rolling,i.e.,normalizing,cold rolling,and tempering (NCT),which was developed to improve the creep strength of the FGHAZ in G115 steel weldments.The NCT treatment effectively promoted the dissolution of preformed M_(23)C_(6)particles and relieved the boundary segregation of C and Cr during welding thermal cycling,which accelerated the dispersed reprecipitation of M_(23)C_(6) particles within the fresh reaustenitized grains during post-weld heat treatment.In addition,the precipitation of Cu-rich phases and MX particles was promoted evidently due to the deformation-induced dislocations.As a result,the interacting actions between precipitates,dislocations,and boundaries during creep were reinforced considerably.Following this strategy,the creep rupture life of the FGHAZ in G115 steel weldments can be prolonged by 18.6%,which can further push the application of G115 steel in USC power plants.展开更多
Lithium-sulfur batteries(LSBs)boasting remarkable energy density have garnered significant attention within academic and industrial spheres.Nevertheless,the progression of LSBs remains constrained by the languid redox...Lithium-sulfur batteries(LSBs)boasting remarkable energy density have garnered significant attention within academic and industrial spheres.Nevertheless,the progression of LSBs remains constrained by the languid redox kinetics intrinsic to sulfur and the pronounced shuttle effect induced by lithium polysulfides(Li PSs),which seriously affecting the energy density,cycling life and rate capacity.The conceptualization and implementation of catalytic materials stand acknowledged as a propitious stratagem for orchestrating kinetic modulation,particularly in excavating the conversion of LiPSs and has evolved into a focal point for disposing.Among them,chalcogenide catalytic materials(CCMs)have shown satisfactory catalytic effects ascribe to the unique physicochemical properties,and have been extensively developed in recent years.Considering the lack of systematic summary regarding the development of CCMs and corresponding performance optimization strategies,herein,we initiate a comprehensive review regarding the recent progress of CCMs for effective collaborative immobilization and accelerated transformation kinetics of Li PSs.Following that,the modulation strategies to improve the catalytic activity of CCMs are summarized,including structural engineering(morphology engineering,surface/interface engineering,crystal engineering)and electronic engineering(doping and vacancy,etc.).Finally,the application prospect of CCMs in LSBs is clarified,and some enlightenment is provided for the reasonable design of CCMs serving practical LSBs.展开更多
In view of the problem that the practical teaching in engineering colleges is out of line with the needs of enterprises, this paper probes into the practical teaching model based on the pilot-scale industry-university...In view of the problem that the practical teaching in engineering colleges is out of line with the needs of enterprises, this paper probes into the practical teaching model based on the pilot-scale industry-university cooperation base. Through the exploration of the practical teaching mode of industry-university cooperation with the pilot-scale base as the core, the students' learning enthusiasm, practical ability, innovative thinking, professional quality and other aspects have been greatly improved, which meets the current demand of enterprises for applied engineering talents and has strong employment competitiveness.展开更多
This study aims to achieve a synergy of strength and ductility in magnesium-based nanocomposite materials through the design of a dual-heterostructure. Utilizing ball milling and hot extrusion, a nano-TiC/AZ61 composi...This study aims to achieve a synergy of strength and ductility in magnesium-based nanocomposite materials through the design of a dual-heterostructure. Utilizing ball milling and hot extrusion, a nano-TiC/AZ61 composite featuring particle-rare coarse grain (CG) and particle-rich fine grain (FG) zones was successfully fabricated. Experimental results demonstrated that compared with the homogeneous structure, the dual-heterostructure composite achieved a significant increase in elongation by 116 % and a remarkable 165 % improvement in the strength-ductility product (SDP), while maintaining a high ultimate tensile strength (UTS) of 417±4 MPa. This substantial performance enhancement is primarily attributed to the additional strain hardening induced by hetero-deformation-induced (HDI) strain hardening and crack-blunting capabilities, as elucidated by microstructural characterization and crystal plasticity finite element modeling (CPFEM). Notably, the strain hardening contribution from the CG zones at the early stage of deformation (≤ 45 % of total plastic deformation amount) is minimal but increases significantly during the subsequent deformation stages. The dislocation increment rate in CG zones (219 %) is observed to be more than double that in FG zones (95 %), attributed to the large grain size and low dislocation density in CG zones, which provide more space for dislocation storage. In addition, the aggravated deformation inhomogeneity as deformation progresses leads to an increase in geometrically necessary dislocations (GNDs) generation near the heterogeneous interface, thereby enhancing HDI hardening. Fracture mechanism analysis indicated that the cracks mainly initiate in the FG region and are effectively blunted upon their propagation to the CG region, necessitating increased energy consumption and indicating higher fracture toughness for the dual-heterostructure composites. This study validates the effectiveness of the dual-heterostructure design in magnesium-based composites, providing a novel understanding of the deformation mechanism through both experimental analysis and CPFEM, paving the way for the development of high-performance, lightweight structural materials.展开更多
In this work,the rare-earth doped ternary lead zirconate titanate ceramics with chemical formula of[0.3 Pb(Zn_(1/3)Nb_(2/3))O_(3)-0.7Pb(Zr_(0.52)Ti_(0.48))O_(3)]+x wt%CeO_(2)(x=0-0.5,abbreviated as 0.3PZN-0.7PZT-xCe)w...In this work,the rare-earth doped ternary lead zirconate titanate ceramics with chemical formula of[0.3 Pb(Zn_(1/3)Nb_(2/3))O_(3)-0.7Pb(Zr_(0.52)Ti_(0.48))O_(3)]+x wt%CeO_(2)(x=0-0.5,abbreviated as 0.3PZN-0.7PZT-xCe)were synthesized by a conventional solid-state reaction route,specific attentions was focused on the effects of CeO_(2)dopants on the structures and electrical properties of the 0.3PZN-0.7PZT ceramics,revealing the role conve rsion of CeO_(2)dopants with its doping amount(x).When less CeO_(2)(x≤0.2)is introduced into 0.3PZN-0.7PZT,the prepared ceramics are identified as the coexistence of rhombohedral and tetragonal phases,also involved with an increased grain size and a reduced atomic ratio of Pb/(Zr+Ti+Zn+Nb).The increased remanent polarization(Pr)and deceased coercive filed(Ec),as well as improved dielectric permittivity(er)and piezoelectric coefficient(d_(33))de monstrate the donor substitution of Ce^(3+)for Pb^(2+)at the A-site of perovskite lattice.Conversely,the introduction of excessive CeO_(2)(x>0.2)causes a reversal evolution in the electrical properties of ceramics,suggesting that some of the introduced cerium element tends to become Ce4+,which equivalently substitutes for Zr^(4+)at the B-site.Additionally,the diffused phase transition(DPT)behaviors of the 0.3PZN-0.7PZT-xCe ceramics were investigated by the modified Curie-Weiss Law.The sample with x=0.2 shows reduced DPT character and optimized electrical properties,including TC=297℃,εr=1400,d_(33)=480 pC/N,tanδ=1.6%,kp=65%,d_(33)·g_(33)=16.32×10^(-12)m^(2)/N,Pr=38.3μC/cm^(2)and Ec=1.02 kV/mm.These enhanced electrical properties not only are contributed by the donor substitution effect of Ce^(3+),but also benefit from the optimized morphotropic phase boundary that is close to the tetragonal-rich side.展开更多
To ensure the safety of power energy transmission channel and mitigate the harm caused by galloping of iced transmission lines,the axial time-delay velocity feedback strategy is adopted to suppress the galloping.The p...To ensure the safety of power energy transmission channel and mitigate the harm caused by galloping of iced transmission lines,the axial time-delay velocity feedback strategy is adopted to suppress the galloping.The par-tial differential equation of galloping with axial time-delay velocity feedback strategy is established based on the variational principle for Hamiltonian.Then,the partial differential equation of galloping is transformed into or-dinary differential equation based on normalization and the Galerkin method.The primary amplitude-frequency response equation,the first-order steady-state approximate solution,and the harmonic amplitude-frequency re-sponse equation are derived by the multiscale method.The impact of different parameters such as time-delay value,control coefficient,and amplitude of external excitation on the galloping response are analyzed.The am-plitude under the primary resonance exhibits periodicity as time-delay value varies.The amplitude diminishes with increased control coefficient and increases with external excitation.Comprehensive consideration of vari-ous influences of parameters on vibration characteristics is crucial when employing the axial time-delay velocity feedback strategy to suppress galloping.Therefore,to achieve the best vibration suppression effect,it is crucial to adjust the time-delay parameter for modifying the range and amplitude of the resonance zone.The conclusions obtained by this study are expected to advance the refinement of active control techniques for iced transmission lines,and may provide valuable insights for practical engineering applications.展开更多
Ruthenium(Ru)-based electrocatalysts show great promise as substitutes for platinum(Pt)for the alkaline hydrogen evolution reaction(HER)because of their efficient water dissociation capabilities.Nevertheless,the stron...Ruthenium(Ru)-based electrocatalysts show great promise as substitutes for platinum(Pt)for the alkaline hydrogen evolution reaction(HER)because of their efficient water dissociation capabilities.Nevertheless,the strong adsorption of Ru-OH intermediates(Ru-OHad)blocks the active site,leading to unsatisfactory HER performance.In this study,we report a universal ligand-exchange strategy for synthesizing a MOF-on-MOF-derived FeP-CoP heterostructure-anchored Ru single-atom site catalyst(Ru-FeP-CoP/NPC).The obtained catalyst shows a low overpotential(28 mV at 10 mA cm^(-2))and a high mass activity(9.29 A mg^(-1) at 100 mV),surpassing the performance of commercial Pt/C by a factor of 46.Theoretical studies show that regulating the local charge distribution of Ru single-atom sites could alleviate surrounding OH-blockages,accelerating water dissociation and facilitating hydrogen adsorption/desorption,thus enhancing HER activity.This work aims to inspire further design of highly active and durable electrocatalysts with tailored electronic properties for high-purity hydrogen production.展开更多
The rational construction of heterogeneous interfacial engineering presents a critical strategy for advancing efficient electrochemical water-splitting development.Here,a bimetallic sulfide-coupled MoNi alloy heterost...The rational construction of heterogeneous interfacial engineering presents a critical strategy for advancing efficient electrochemical water-splitting development.Here,a bimetallic sulfide-coupled MoNi alloy heterostructure catalyst(VMoS/MoNi)is synthesized via hydrothermal and sulfidation methods for high-performance alkaline water electrolysis.Benefiting from interfacial coupling within the VMoS/MoNi catalyst,the active sites are enriched,and electron transfer is promoted,leading to enhanced synergy and collaboration in electrocatalytic reactions.As a result,at 10 mA·cm^(-2),the VMoS/MoNi catalyst demonstrates excellent HER(26 mV)and OER(223 mV)performance.VMoS/MoNi catalysts used as double electrode in an alkaline electrolytic assembly are noteworthy for achieving a cell voltage of 1.56 V at 10 mA·cm^(-2),a significant improvement above most previously reported bifunctional electrocatalysts.This result provides further momentum for the design of heterostructure electrocatalysts,advancing the study of renewable energy conversion and storage.展开更多
Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising ph...Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising photocatalysts for H_(2)O_(2)production due to their unique electronic,optical properties,and tunable structures.However,the high exciton binding energy of CPs hinders efficient exciton dissociation and charge separation,limiting their photocatalytic performance.In this work,we synthesized scandium(Sc)atoms decorated CPs with enhanced ordered stacking and crystallinity by introducing benzaldehyde as an end-capping reagent.The strong interaction between charged Sc atoms and electrons facilitates exciton dissociation and improves charge transfer capability.Furthermore,the Lewis acidic nature of Sc atoms promotes oxygen adsorption and enhances the stabilization of superoxide anion intermediate(·O_(2)^(-)).As a result,the as-synthesized photocatalysts exhibit a high H_(2)O_(2)production rate of 18μmol h^(-1)in pure water,which is three times that of pristine CPs,This work provides valuable insights into the design of organic polymer photocatalysts for various photocatalytic reactions.展开更多
Molybdenum(Mo) alloys with different La_(2)O_(3)particle additions(0.6,0.9,1.5 wt.%) were prepared by powder metallurgy to investigate the effect of La_(2)O_(3)particles on microstructural evolution and creep behavior...Molybdenum(Mo) alloys with different La_(2)O_(3)particle additions(0.6,0.9,1.5 wt.%) were prepared by powder metallurgy to investigate the effect of La_(2)O_(3)particles on microstructural evolution and creep behavior of the alloy.Pure Mo,annealed at 1500℃ for 1 h,presented a fully recrystallized microstructure characterized by equiaxed grains.The alloys doped with La_(2)O_(3)particles(Mo-La_(2)O_(3)alloys),on the other hand,exhibited fibrous grains elongated in the rolling direction of the plate.In contrast to the shape of the grains,the average grain size of the alloys was found to be insensitive to the addition of La_(2)O_(3)particles.Nanosized La_(2)O_(3)particles with diameters ranging from 65 to 75 nm were distributed within the grain interior.Tensile creep tests showed that dislocation creep was the predominant deformation mode at intermediate creep rate(10^(-7)s^(-1)-10^(-4)s^(-1)) in the present alloys.The creep stress exponent and activation energy were found to decrease with increasing temperature,particularly within the low creep rate regime(<10^(-7)s^(-1)).The Mo-La_(2)O_(3)alloys exhibited remarkably greater apparent stress exponent and activation energy than pure Mo.A creep constitutive model based on the interaction between particles and dislocations was utilized to rationalize the nanoparticle-improved creep behavior.It was demonstrated that low relaxed efficiency of dislocation line energy,which is responsible for an enhanced climb resistance of dislocations,is the major creep strengthening mechanism in the Mo-La_(2)O_(3)alloys.In addition,the area reduction and creep fracture mode of the Mo-La_(2)O_(3)alloys were found to be a function of the creep rate and temperature,which can be explained by the effect of the two parameters on the creep and fracture mechanisms.展开更多
A method for reliability analysis of the competing failure with the probabilistic failure threshold value not the fixed threshold value is presented, which involves the random shocks and the degradation is independent...A method for reliability analysis of the competing failure with the probabilistic failure threshold value not the fixed threshold value is presented, which involves the random shocks and the degradation is independent and dependent respectively. Specifically, for the dependent condition, the effect due to the random shocks on the degradation is considered with a damage factor. In addition, the dependent competing failure model is applied to the reliability analysis of the k-out-of-n systems. Finally, two studied cases are presented to illustrate the proposed method, and the results show the proposed method is reasonable.展开更多
The internal mechanism of the high hydrophobicity of the coal samples from the Pingdingshan mining area was studied through industrial,element,and surface functional group analysis.Laboratory testing and molecular dyn...The internal mechanism of the high hydrophobicity of the coal samples from the Pingdingshan mining area was studied through industrial,element,and surface functional group analysis.Laboratory testing and molecular dynamics simulations were employed to study the impact of three types of surfactants on the surface adsorption properties and wettability of highly hydrophobic bituminous coal.The results show that the surface of highly hydrophobic bituminous coal is compact,rich in inorganic minerals,and poorly wettable and that coal molecules are dominated by hydrophobic functional groups of aromatic rings and aliphatic structures.The wetting performance of surfactants as the intermediate carrier to connect coal and water molecules is largely determined by the interaction force between surfactants and coal(Fs-c)and the interaction force between surfactants and water(Fs-w),which effectively improve the wettability of modified coal dust via modifying its surface electrical properties and surface energy.A new type of wetting agent with a dust removal rate of 89%has been developed through discovery of a compound wetting agent solution with optimal wetting and settling performance.This paper provides theoretical and technical support for removing highly hydrophobic bituminous coal dust in underground mining.展开更多
The oxide dispersion strengthened Mo alloys(ODS-Mo)prepared by traditional ball milling and subsequent sintering technique generally possess comparatively coarse Mo grains and large oxide particles at Mo grain boundar...The oxide dispersion strengthened Mo alloys(ODS-Mo)prepared by traditional ball milling and subsequent sintering technique generally possess comparatively coarse Mo grains and large oxide particles at Mo grain boundaries(GBs),which obviously suppress the corresponding strengthening effect of oxide addition.In this work,the Y_(2)O_(3) and TiC particles were simultaneously doped into Mo alloys using ball-milling and subsequent low temperature sintering.Accompanied by TiC addition,the Mo-Y_(2)O_(3) grains are sharply refined from 3.12 to 1.36μm.In particular,Y_(2)O_(3) and TiC can form smaller Y-Ti-O-C quaternary phase particles(~230 nm)at Mo GBs compared to single Y_(2)O_(3) particles(~420 nm),so as to these new formed Y-Ti-O-C particles can more effectively pin and hinder GBs movement.In addition to Y-Ti-O-C particles at GBs,Y_(2)O_(3),TiOx,and TiCx nanoparticles(<100 nm)also exist within Mo grains,which is significantly different from traditional ODS-Mo.The appearance of TiOx phase indicates that some active Ti within TiC can adsorb oxygen impurities of Mo matrix to form a new strengthening phase,thus strengthening and purifying Mo matrix.Furthermore,the pure Mo,Mo-Y_(2)O_(3),and Mo-Y_(2)O_(3)-TiC alloys have similar relative densities(97.4%-98.0%).More importantly,the Mo-Y_(2)O_(3)-TiC alloys exhibit higher hardness(HV0.2(425±25))compared to Mo-Y_(2)O_(3) alloys(HV0.2(370±25)).This work could provide a relevant strategy for the preparation of ultrafine Mo alloys by facile ball-milling.展开更多
Dwell fatigue effect is a long-standing problem threatening the long-term service reliability for fan blades and fan disks of an aircraft engine.To understand the basic mechanism of dwell fatigue damage,pure fatigue a...Dwell fatigue effect is a long-standing problem threatening the long-term service reliability for fan blades and fan disks of an aircraft engine.To understand the basic mechanism of dwell fatigue damage,pure fatigue and 60 s dwell fatigue properties of bimodal Ti-6Al-4V alloys with different volume fractions of the primaryα(α_(p))phase were examined comparatively.The results showed that both pure fatigue and dwell fatigue life decreased with increasing the volume fraction of theα_(p)phase and the dwell fatigue life was lower than the pure fatigue one.The quasi-in-situ test results and the quantitative characterization of damage behaviors of the local microstructure units defined by theα_(p)-secondaryα(α_(s))combination reveal that theα_(s)phase close to theα_(p)phase with extensively slip activities was gradually damaged under dwell fatigue loading,while that under pure fatigue loading was undamaged,demonstrating that the dwell loading induced the damage of theα_(s)phase,and further reduced the fatigue life.A stress relaxation-based model is proposed to describe the physical mechanism on dwell fatigue damage of the bimodal Ti-6Al-4V alloy,i.e.the elastic deformation of theα_(s)phase caused by the strain incompatibility would be gradually transformed into plastic deformation during the dwell stage,and thus promotes fatigue damage.The model provides new insights into the microscopic process of stress/strain transfer between the soft and hard microstructure units under dwell fatigue loading.展开更多
Phosphogypsum is a solid waste sourced from the wet-process phosphoric acid industry,which causes severe environmental damages.Its utilization was limited by its high decomposition temperature and high energy consumpt...Phosphogypsum is a solid waste sourced from the wet-process phosphoric acid industry,which causes severe environmental damages.Its utilization was limited by its high decomposition temperature and high energy consumption.Herein,an Fe-P slag,which is a solid waste that mainly comprises iron phosphide(FeP)and diiron phosphide(Fe_(2)P),can dramatically decrease the decomposition temperature of phosphogypsum.It was found that the Fe-P slag and CaSO_(4) can react as shown in the following reaction equation:2Fe_(1.5)P+3CaSO_(4)+6CO_(2)→Ca_(3)(PO_(4))_(2)+Fe_(3)O_(4)+3SO_(2)+6CO.Its reaction mechanism was further determined using the thermodynamic method.It was found that CaS was the key intermediate for this reaction.The CaSO_(4) conversion for this method can reach approximately 97%under the optimized roasting conditions:the molar ratio between Fe_(1.5) P and CaSO_(4) of 2:3,roasting temperature of 900℃,a roasting time of 8 h.展开更多
OER catalyst of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C(NiFeSC series)mixed crystal composite nanofibers was prepared by electrospinning and atmospheric heat treatment process.The testing results indicate that the diameters of Ni_(...OER catalyst of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C(NiFeSC series)mixed crystal composite nanofibers was prepared by electrospinning and atmospheric heat treatment process.The testing results indicate that the diameters of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite nanofibers is about 200 nm,the grains size is about 1-3 nm,and the fiber surface is rough.The electrochemical test results show that the heterojunction of the prepared Ni_(3)Fe/Ni_(4)S_(3)/Ni/C hybrid crystal composite nanofiber has synergistic effect with sulfide,and exhibits good electrocatalytic activity of water decomposition and OER in alkaline system.The OER electrocatalytic performance of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite electrode prepared via a heat treatment at 1000℃process was tested in 1 mol/L KOH electrolytes.The results show that the overpotential is about 298 mV,the Tafel slope is about 74 mV?dec-1,and the surface resistance is about 1.69Ω·cm^(2),at the current density of 10 mA·cm^(-2).展开更多
Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity.However,their cycling performance ...Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity.However,their cycling performance is impeded by their instability caused by the reaction mechanism.Herein,we report the engineering and synthesis of a novel hybrid architecture composed of MoO2.0N0.5 atomic nanoclusters bonded in nanosheets of N-doped carbon hierarchical hollow microspheres(MoO2.0N0.5/NC)as an anode material for sodium-ion batteries.The facile self-templating strategy for the synthesis of MoO2.0N0.5/NC involves chemical polymerization and subsequent one-step calcination treatments.The design is benefi-cial to improve the electrochemical kinetics,buffer the volume variation of electrodes during cycling,and provide more interfacial active sites for sodium uptake.Due to these unique structural and compositional merits,these MoO2.0N0.5/NC exhibits excellent sodium storage performance in terms of superior rate capability and stable long cycle life.The work shows a feasible and effective way to design novel host candidates and solve the long-term cycling stability issues for sodium-ion batteries.展开更多
Red emitting phosphors play a significant role in accelerating the improvement of illumination quality for white light emitting diodes(WLEDs).In this work,by using solid-state reaction method,an efficient novel Ba_(2)...Red emitting phosphors play a significant role in accelerating the improvement of illumination quality for white light emitting diodes(WLEDs).In this work,by using solid-state reaction method,an efficient novel Ba_(2)LuNbO_(6):Eu^(3+)phosphor with double-perovskite structure was successfully prepared.Here,a series of Ba_(2)LuNbO_(6):Eu^(3+)red phosphors can be efficiently pumped by the near-ultraviolet(UV)light and then present high-brightness at orange emission(598 nm,~5D_(0)→~7 F_(1))and red emission(610 nm,~5D_(0)→~7 F_(2)).The ratio values of 610 to 598 nm in Ba_(2)LuNbO_(6):Eu^(3+)phosphors exceed 1 when the content of Eu^(3+)is larger than 0.4 mol,because the occupation of Eu^(3+)ions is changed from Lu^(3+)ions with symmetric sites to Ba^(2+)ions with asymmetric sites.Besides,the optimized concentration of Eu^(3+)at the~5D_(0)→~7 F_(2)transitions is obtained when x=1,indicating that there is non-concentration quenching in Ba_(2)LuNbO_(6):Eu^(3+)phosphors.Moreover,the CIE chromaticity coordinates of Ba_(2)LuNbO_(6):Eu^(3+)was calculated to be(0.587,0.361),the color purity was calculated to be 72.26%and internal quenching efficiency(IQE)was measured to be 67%.Finally,the thermal stability of Ba_(2)LuNbO_(6):Eu^(3+)phosphors was also studied.Our work demonstrates that the novel double-perovskite red-emitting Ba_(2)LuNbO_(6):Eu^(3+)phosphors are prospective red emitting elements for WLEDs applications.展开更多
In the present study,porous bulk palladium samples were prepared by sodium chloride salt powder spacer incorporation and removal combined with dealloying.The obtained porous Pd bulks were characterized by X‐ray diffr...In the present study,porous bulk palladium samples were prepared by sodium chloride salt powder spacer incorporation and removal combined with dealloying.The obtained porous Pd bulks were characterized by X‐ray diffraction,field‐emission scanning electron microscopy and N2adsorption isotherm measurements.The prepared porous Pd bulk samples showed a hierarchical pore structure,a high porosity of^88%,a high surface area of^54m2/g,and a compression strength of^0.5MPa.Electrochemical measurements were performed to evaluate the electrocatalytic properties of the porous Pd bulk samples,revealing their effectiveness for ethanol oxidation.展开更多
基金supported by Guangdong Basic and Applied Basic Research Foundation and Project of General Colleges and Universities in Guangdong Province(Nos.2022A1515140002 and 2019GKQNCX127)the Special Innovation Projects of Department of Education’s of Guangdong Provincial(No.2018KTSCX220)+4 种基金the International Cooperation Project of Guangdong Province(No.2019A050510049)the Program for Innovative Research Team of Guangdong Province&Huizhou University(IRTHZU)Indigenous Innovation’s Capability Development Program of Huizhou University(No.HZU202014)the Open Project Program of Guangdong Provincial Key Laboratory of Electronic Functional Materials and Devices,Huizhou University(No.EFMD2022015M)the National Natural Science Foundation of China(No.12102068).
文摘High-entropy perovskite ferroelectric materials have attracted significant attention due to their remarkably low remnant polarizations and narrow hysteresis.Thus,these materials offer high-energy density and efficiency,making them suitable for energy storage applications.Despite significant advancements in experimental research,understanding of the properties associated with structure remains incomplete.This study aims to study the structural,electric,and mechanical performances at various scales of the high-entropy(Na_(0.2)Bi_(0.2)Ca_(0.2)Sr_(0.2)Ba_(0.2))TiO_(3)(NBCSB)material.The results of first-principles calculations indicated that the pseudo-intralayer distortion was obviously smaller compared to the interlayer distortion.Among the various bonds,Bi-O,Ca-O,and Na-O experienced the greatest displacement.Similarly,the hybridization between O 2p and Ti 3d states with Bi 6p states was particularly strong,affecting both the ferroelectric polarization and relaxor behavior.The NBCSB materials produced using a typical solid-state process demonstrated exceptional performance in energy storage with a recoverable density of 1.53 J·cm^(-3)and a high efficiency of 89%when subjected to a small electric field of 120 kV·cm^(-1).In addition,these ceramics displayed a remarkable hardness of around 7.23 GPa.NBCSB ceramics exhibited exceptional relaxation characteristics with minimal hysteresis and low remanent polarization due to its nanoscale high dynamic polarization configuration with diverse symmetries(rhombohedral,tetragonal,and cubic)resulting from randomly dispersed A-site ions.The excellent mechanical property is related to the dislocation-blocking effect,solid solution strengthening effect,and domain boundary effect.The findings of this study offer a comprehensive and novel perspective on A-site disordered high-entropy relaxor ferroelectric ceramics.
基金financially supported by the National Key R&D Program of China(No.2022YFB3705300)the National Natural Science Foundation of China(Nos.U1960204 and 51974199)the Postdoctoral Fellowship Program of CPSF(No.GZB20230515)。
文摘The infamous type Ⅳ failure within the fine-grained heat-affected zone (FGHAZ) in G115 steel weldments seriously threatens the safe operation of ultra-supercritical (USC) power plants.In this work,the traditional thermo-mechanical treatment was modified via the replacement of hot-rolling with cold rolling,i.e.,normalizing,cold rolling,and tempering (NCT),which was developed to improve the creep strength of the FGHAZ in G115 steel weldments.The NCT treatment effectively promoted the dissolution of preformed M_(23)C_(6)particles and relieved the boundary segregation of C and Cr during welding thermal cycling,which accelerated the dispersed reprecipitation of M_(23)C_(6) particles within the fresh reaustenitized grains during post-weld heat treatment.In addition,the precipitation of Cu-rich phases and MX particles was promoted evidently due to the deformation-induced dislocations.As a result,the interacting actions between precipitates,dislocations,and boundaries during creep were reinforced considerably.Following this strategy,the creep rupture life of the FGHAZ in G115 steel weldments can be prolonged by 18.6%,which can further push the application of G115 steel in USC power plants.
基金financially supported by the National Natural Science Foundation of China(No.U21A2077)the Taishan Scholar Project Foundation of Shandong Province(No.ts20190908)+1 种基金the Natural Science Foundation of Shandong Province(No.ZR2021ZD05)the China Postdoctoral Science Foundation(Nos.2023TQ0192,2023M742065)。
文摘Lithium-sulfur batteries(LSBs)boasting remarkable energy density have garnered significant attention within academic and industrial spheres.Nevertheless,the progression of LSBs remains constrained by the languid redox kinetics intrinsic to sulfur and the pronounced shuttle effect induced by lithium polysulfides(Li PSs),which seriously affecting the energy density,cycling life and rate capacity.The conceptualization and implementation of catalytic materials stand acknowledged as a propitious stratagem for orchestrating kinetic modulation,particularly in excavating the conversion of LiPSs and has evolved into a focal point for disposing.Among them,chalcogenide catalytic materials(CCMs)have shown satisfactory catalytic effects ascribe to the unique physicochemical properties,and have been extensively developed in recent years.Considering the lack of systematic summary regarding the development of CCMs and corresponding performance optimization strategies,herein,we initiate a comprehensive review regarding the recent progress of CCMs for effective collaborative immobilization and accelerated transformation kinetics of Li PSs.Following that,the modulation strategies to improve the catalytic activity of CCMs are summarized,including structural engineering(morphology engineering,surface/interface engineering,crystal engineering)and electronic engineering(doping and vacancy,etc.).Finally,the application prospect of CCMs in LSBs is clarified,and some enlightenment is provided for the reasonable design of CCMs serving practical LSBs.
文摘In view of the problem that the practical teaching in engineering colleges is out of line with the needs of enterprises, this paper probes into the practical teaching model based on the pilot-scale industry-university cooperation base. Through the exploration of the practical teaching mode of industry-university cooperation with the pilot-scale base as the core, the students' learning enthusiasm, practical ability, innovative thinking, professional quality and other aspects have been greatly improved, which meets the current demand of enterprises for applied engineering talents and has strong employment competitiveness.
基金support from the China Scholarship Council(No.202107000038)support from the National Natural Science Foundation of China(Nos.52004227,52061040,and 12222209)the China Postdoctoral Science Foundation(No:2021M692512).
文摘This study aims to achieve a synergy of strength and ductility in magnesium-based nanocomposite materials through the design of a dual-heterostructure. Utilizing ball milling and hot extrusion, a nano-TiC/AZ61 composite featuring particle-rare coarse grain (CG) and particle-rich fine grain (FG) zones was successfully fabricated. Experimental results demonstrated that compared with the homogeneous structure, the dual-heterostructure composite achieved a significant increase in elongation by 116 % and a remarkable 165 % improvement in the strength-ductility product (SDP), while maintaining a high ultimate tensile strength (UTS) of 417±4 MPa. This substantial performance enhancement is primarily attributed to the additional strain hardening induced by hetero-deformation-induced (HDI) strain hardening and crack-blunting capabilities, as elucidated by microstructural characterization and crystal plasticity finite element modeling (CPFEM). Notably, the strain hardening contribution from the CG zones at the early stage of deformation (≤ 45 % of total plastic deformation amount) is minimal but increases significantly during the subsequent deformation stages. The dislocation increment rate in CG zones (219 %) is observed to be more than double that in FG zones (95 %), attributed to the large grain size and low dislocation density in CG zones, which provide more space for dislocation storage. In addition, the aggravated deformation inhomogeneity as deformation progresses leads to an increase in geometrically necessary dislocations (GNDs) generation near the heterogeneous interface, thereby enhancing HDI hardening. Fracture mechanism analysis indicated that the cracks mainly initiate in the FG region and are effectively blunted upon their propagation to the CG region, necessitating increased energy consumption and indicating higher fracture toughness for the dual-heterostructure composites. This study validates the effectiveness of the dual-heterostructure design in magnesium-based composites, providing a novel understanding of the deformation mechanism through both experimental analysis and CPFEM, paving the way for the development of high-performance, lightweight structural materials.
基金Project supported by the Natural Science Foundation of Sichuan Province(2024NSFSC0219)。
文摘In this work,the rare-earth doped ternary lead zirconate titanate ceramics with chemical formula of[0.3 Pb(Zn_(1/3)Nb_(2/3))O_(3)-0.7Pb(Zr_(0.52)Ti_(0.48))O_(3)]+x wt%CeO_(2)(x=0-0.5,abbreviated as 0.3PZN-0.7PZT-xCe)were synthesized by a conventional solid-state reaction route,specific attentions was focused on the effects of CeO_(2)dopants on the structures and electrical properties of the 0.3PZN-0.7PZT ceramics,revealing the role conve rsion of CeO_(2)dopants with its doping amount(x).When less CeO_(2)(x≤0.2)is introduced into 0.3PZN-0.7PZT,the prepared ceramics are identified as the coexistence of rhombohedral and tetragonal phases,also involved with an increased grain size and a reduced atomic ratio of Pb/(Zr+Ti+Zn+Nb).The increased remanent polarization(Pr)and deceased coercive filed(Ec),as well as improved dielectric permittivity(er)and piezoelectric coefficient(d_(33))de monstrate the donor substitution of Ce^(3+)for Pb^(2+)at the A-site of perovskite lattice.Conversely,the introduction of excessive CeO_(2)(x>0.2)causes a reversal evolution in the electrical properties of ceramics,suggesting that some of the introduced cerium element tends to become Ce4+,which equivalently substitutes for Zr^(4+)at the B-site.Additionally,the diffused phase transition(DPT)behaviors of the 0.3PZN-0.7PZT-xCe ceramics were investigated by the modified Curie-Weiss Law.The sample with x=0.2 shows reduced DPT character and optimized electrical properties,including TC=297℃,εr=1400,d_(33)=480 pC/N,tanδ=1.6%,kp=65%,d_(33)·g_(33)=16.32×10^(-12)m^(2)/N,Pr=38.3μC/cm^(2)and Ec=1.02 kV/mm.These enhanced electrical properties not only are contributed by the donor substitution effect of Ce^(3+),but also benefit from the optimized morphotropic phase boundary that is close to the tetragonal-rich side.
基金supported by the National Natural Science Foundation of China(Grant No.51507106)China Postdoctoral Science Foundation(Grant No.2021M702371)。
文摘To ensure the safety of power energy transmission channel and mitigate the harm caused by galloping of iced transmission lines,the axial time-delay velocity feedback strategy is adopted to suppress the galloping.The par-tial differential equation of galloping with axial time-delay velocity feedback strategy is established based on the variational principle for Hamiltonian.Then,the partial differential equation of galloping is transformed into or-dinary differential equation based on normalization and the Galerkin method.The primary amplitude-frequency response equation,the first-order steady-state approximate solution,and the harmonic amplitude-frequency re-sponse equation are derived by the multiscale method.The impact of different parameters such as time-delay value,control coefficient,and amplitude of external excitation on the galloping response are analyzed.The am-plitude under the primary resonance exhibits periodicity as time-delay value varies.The amplitude diminishes with increased control coefficient and increases with external excitation.Comprehensive consideration of vari-ous influences of parameters on vibration characteristics is crucial when employing the axial time-delay velocity feedback strategy to suppress galloping.Therefore,to achieve the best vibration suppression effect,it is crucial to adjust the time-delay parameter for modifying the range and amplitude of the resonance zone.The conclusions obtained by this study are expected to advance the refinement of active control techniques for iced transmission lines,and may provide valuable insights for practical engineering applications.
基金supported by the National Natural Science Foundation of China(22369025)Yunnan Applied Basic Research Projects(202201AT070095,202301AT070098,202301AT070107,202401AT070438,202401AT070433)+2 种基金the 3rd Professional Degree Graduate Practice Innovation Project of Yunnan University(ZC-23235291,ZC-23234269,KC-23236398,KC-23234063)the Education Reform Research Project of Yunnan University(No.2021Z06)the Xingdian Talent Program of Yunnan Province,and the Yunnan Revitalization Talent Support Program.
文摘Ruthenium(Ru)-based electrocatalysts show great promise as substitutes for platinum(Pt)for the alkaline hydrogen evolution reaction(HER)because of their efficient water dissociation capabilities.Nevertheless,the strong adsorption of Ru-OH intermediates(Ru-OHad)blocks the active site,leading to unsatisfactory HER performance.In this study,we report a universal ligand-exchange strategy for synthesizing a MOF-on-MOF-derived FeP-CoP heterostructure-anchored Ru single-atom site catalyst(Ru-FeP-CoP/NPC).The obtained catalyst shows a low overpotential(28 mV at 10 mA cm^(-2))and a high mass activity(9.29 A mg^(-1) at 100 mV),surpassing the performance of commercial Pt/C by a factor of 46.Theoretical studies show that regulating the local charge distribution of Ru single-atom sites could alleviate surrounding OH-blockages,accelerating water dissociation and facilitating hydrogen adsorption/desorption,thus enhancing HER activity.This work aims to inspire further design of highly active and durable electrocatalysts with tailored electronic properties for high-purity hydrogen production.
基金supported by the National Natural Science Foundation of China(No.22369025)Yunnan Applied Basic Research Projects(Nos.202201AT070095,202301AT070098,202301AT070107,202401AT070438,and 202401AT070433)+2 种基金Education Reform Research Project of Yunnan University(No.2021Z06)Yunnan University Graduate Student Practice and Innovation Program(Nos.ZC-23234269,ZC-23235291,KC-23236398,and KC-23234063)Yunnan Revitalization Talent Support Program。
文摘The rational construction of heterogeneous interfacial engineering presents a critical strategy for advancing efficient electrochemical water-splitting development.Here,a bimetallic sulfide-coupled MoNi alloy heterostructure catalyst(VMoS/MoNi)is synthesized via hydrothermal and sulfidation methods for high-performance alkaline water electrolysis.Benefiting from interfacial coupling within the VMoS/MoNi catalyst,the active sites are enriched,and electron transfer is promoted,leading to enhanced synergy and collaboration in electrocatalytic reactions.As a result,at 10 mA·cm^(-2),the VMoS/MoNi catalyst demonstrates excellent HER(26 mV)and OER(223 mV)performance.VMoS/MoNi catalysts used as double electrode in an alkaline electrolytic assembly are noteworthy for achieving a cell voltage of 1.56 V at 10 mA·cm^(-2),a significant improvement above most previously reported bifunctional electrocatalysts.This result provides further momentum for the design of heterostructure electrocatalysts,advancing the study of renewable energy conversion and storage.
基金supported by the Natural Science Foundation of China(22408278,22275139,21971190,U21A2077)the Key Project of Natural Science Foundation of Tianjin City(Contract No.22JCZDJC00510)Key Laboratory of Functional Inorganic Material Chemistry(Heilongjiang University),Ministry of Education。
文摘Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising photocatalysts for H_(2)O_(2)production due to their unique electronic,optical properties,and tunable structures.However,the high exciton binding energy of CPs hinders efficient exciton dissociation and charge separation,limiting their photocatalytic performance.In this work,we synthesized scandium(Sc)atoms decorated CPs with enhanced ordered stacking and crystallinity by introducing benzaldehyde as an end-capping reagent.The strong interaction between charged Sc atoms and electrons facilitates exciton dissociation and improves charge transfer capability.Furthermore,the Lewis acidic nature of Sc atoms promotes oxygen adsorption and enhances the stabilization of superoxide anion intermediate(·O_(2)^(-)).As a result,the as-synthesized photocatalysts exhibit a high H_(2)O_(2)production rate of 18μmol h^(-1)in pure water,which is three times that of pristine CPs,This work provides valuable insights into the design of organic polymer photocatalysts for various photocatalytic reactions.
基金supported by the National Natural Science Foundation of China (Grant Nos.,51801147,and 51901173)supported by the International Joint Laboratory for Micro/Nano Manufacturing and Measurement Technologies。
文摘Molybdenum(Mo) alloys with different La_(2)O_(3)particle additions(0.6,0.9,1.5 wt.%) were prepared by powder metallurgy to investigate the effect of La_(2)O_(3)particles on microstructural evolution and creep behavior of the alloy.Pure Mo,annealed at 1500℃ for 1 h,presented a fully recrystallized microstructure characterized by equiaxed grains.The alloys doped with La_(2)O_(3)particles(Mo-La_(2)O_(3)alloys),on the other hand,exhibited fibrous grains elongated in the rolling direction of the plate.In contrast to the shape of the grains,the average grain size of the alloys was found to be insensitive to the addition of La_(2)O_(3)particles.Nanosized La_(2)O_(3)particles with diameters ranging from 65 to 75 nm were distributed within the grain interior.Tensile creep tests showed that dislocation creep was the predominant deformation mode at intermediate creep rate(10^(-7)s^(-1)-10^(-4)s^(-1)) in the present alloys.The creep stress exponent and activation energy were found to decrease with increasing temperature,particularly within the low creep rate regime(<10^(-7)s^(-1)).The Mo-La_(2)O_(3)alloys exhibited remarkably greater apparent stress exponent and activation energy than pure Mo.A creep constitutive model based on the interaction between particles and dislocations was utilized to rationalize the nanoparticle-improved creep behavior.It was demonstrated that low relaxed efficiency of dislocation line energy,which is responsible for an enhanced climb resistance of dislocations,is the major creep strengthening mechanism in the Mo-La_(2)O_(3)alloys.In addition,the area reduction and creep fracture mode of the Mo-La_(2)O_(3)alloys were found to be a function of the creep rate and temperature,which can be explained by the effect of the two parameters on the creep and fracture mechanisms.
基金the Special Research Fund for the National Natural Science Foundation of China(No.11272082)the Fundamental Research Funds for the Central Universities(No.E022050205)the Open Research Fund of Key Laboratory of Fluid and Power Machinery of Xihua University(No.szjj2013-03)
文摘A method for reliability analysis of the competing failure with the probabilistic failure threshold value not the fixed threshold value is presented, which involves the random shocks and the degradation is independent and dependent respectively. Specifically, for the dependent condition, the effect due to the random shocks on the degradation is considered with a damage factor. In addition, the dependent competing failure model is applied to the reliability analysis of the k-out-of-n systems. Finally, two studied cases are presented to illustrate the proposed method, and the results show the proposed method is reasonable.
文摘The internal mechanism of the high hydrophobicity of the coal samples from the Pingdingshan mining area was studied through industrial,element,and surface functional group analysis.Laboratory testing and molecular dynamics simulations were employed to study the impact of three types of surfactants on the surface adsorption properties and wettability of highly hydrophobic bituminous coal.The results show that the surface of highly hydrophobic bituminous coal is compact,rich in inorganic minerals,and poorly wettable and that coal molecules are dominated by hydrophobic functional groups of aromatic rings and aliphatic structures.The wetting performance of surfactants as the intermediate carrier to connect coal and water molecules is largely determined by the interaction force between surfactants and coal(Fs-c)and the interaction force between surfactants and water(Fs-w),which effectively improve the wettability of modified coal dust via modifying its surface electrical properties and surface energy.A new type of wetting agent with a dust removal rate of 89%has been developed through discovery of a compound wetting agent solution with optimal wetting and settling performance.This paper provides theoretical and technical support for removing highly hydrophobic bituminous coal dust in underground mining.
基金financially supported by the National Natural Science Foundation of China (Nos. 52171044 and 51804218)the Innovation and Entrepreneurship Training Program for College Students in Fujian Province, China (No. S202111312029)
文摘The oxide dispersion strengthened Mo alloys(ODS-Mo)prepared by traditional ball milling and subsequent sintering technique generally possess comparatively coarse Mo grains and large oxide particles at Mo grain boundaries(GBs),which obviously suppress the corresponding strengthening effect of oxide addition.In this work,the Y_(2)O_(3) and TiC particles were simultaneously doped into Mo alloys using ball-milling and subsequent low temperature sintering.Accompanied by TiC addition,the Mo-Y_(2)O_(3) grains are sharply refined from 3.12 to 1.36μm.In particular,Y_(2)O_(3) and TiC can form smaller Y-Ti-O-C quaternary phase particles(~230 nm)at Mo GBs compared to single Y_(2)O_(3) particles(~420 nm),so as to these new formed Y-Ti-O-C particles can more effectively pin and hinder GBs movement.In addition to Y-Ti-O-C particles at GBs,Y_(2)O_(3),TiOx,and TiCx nanoparticles(<100 nm)also exist within Mo grains,which is significantly different from traditional ODS-Mo.The appearance of TiOx phase indicates that some active Ti within TiC can adsorb oxygen impurities of Mo matrix to form a new strengthening phase,thus strengthening and purifying Mo matrix.Furthermore,the pure Mo,Mo-Y_(2)O_(3),and Mo-Y_(2)O_(3)-TiC alloys have similar relative densities(97.4%-98.0%).More importantly,the Mo-Y_(2)O_(3)-TiC alloys exhibit higher hardness(HV0.2(425±25))compared to Mo-Y_(2)O_(3) alloys(HV0.2(370±25)).This work could provide a relevant strategy for the preparation of ultrafine Mo alloys by facile ball-milling.
基金financially supported by the National Natural Science Foundation of China(Nos.51771207 and 52171128)the Fundamental Research Project of Shenyang National Laboratory for Materials Science(No.L2019R18)。
文摘Dwell fatigue effect is a long-standing problem threatening the long-term service reliability for fan blades and fan disks of an aircraft engine.To understand the basic mechanism of dwell fatigue damage,pure fatigue and 60 s dwell fatigue properties of bimodal Ti-6Al-4V alloys with different volume fractions of the primaryα(α_(p))phase were examined comparatively.The results showed that both pure fatigue and dwell fatigue life decreased with increasing the volume fraction of theα_(p)phase and the dwell fatigue life was lower than the pure fatigue one.The quasi-in-situ test results and the quantitative characterization of damage behaviors of the local microstructure units defined by theα_(p)-secondaryα(α_(s))combination reveal that theα_(s)phase close to theα_(p)phase with extensively slip activities was gradually damaged under dwell fatigue loading,while that under pure fatigue loading was undamaged,demonstrating that the dwell loading induced the damage of theα_(s)phase,and further reduced the fatigue life.A stress relaxation-based model is proposed to describe the physical mechanism on dwell fatigue damage of the bimodal Ti-6Al-4V alloy,i.e.the elastic deformation of theα_(s)phase caused by the strain incompatibility would be gradually transformed into plastic deformation during the dwell stage,and thus promotes fatigue damage.The model provides new insights into the microscopic process of stress/strain transfer between the soft and hard microstructure units under dwell fatigue loading.
基金financially supported by the National Natural Science Foundation of China (22108185, 51702027)the Fundamental Research Funds for the Central University in China(20826041B4126)project of Sichuan Chengdu Science and Technology Bureau (2019-YF05-02170-SN)
文摘Phosphogypsum is a solid waste sourced from the wet-process phosphoric acid industry,which causes severe environmental damages.Its utilization was limited by its high decomposition temperature and high energy consumption.Herein,an Fe-P slag,which is a solid waste that mainly comprises iron phosphide(FeP)and diiron phosphide(Fe_(2)P),can dramatically decrease the decomposition temperature of phosphogypsum.It was found that the Fe-P slag and CaSO_(4) can react as shown in the following reaction equation:2Fe_(1.5)P+3CaSO_(4)+6CO_(2)→Ca_(3)(PO_(4))_(2)+Fe_(3)O_(4)+3SO_(2)+6CO.Its reaction mechanism was further determined using the thermodynamic method.It was found that CaS was the key intermediate for this reaction.The CaSO_(4) conversion for this method can reach approximately 97%under the optimized roasting conditions:the molar ratio between Fe_(1.5) P and CaSO_(4) of 2:3,roasting temperature of 900℃,a roasting time of 8 h.
基金Funded by the Doctoral Fund of Chengdu University (2081919131)the Open Fund of Material Corrosion and Protection Key Laboratory of Sichuan Province (2021CL27)the Sichuan Science and Technology Program (2023YFG0229)。
文摘OER catalyst of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C(NiFeSC series)mixed crystal composite nanofibers was prepared by electrospinning and atmospheric heat treatment process.The testing results indicate that the diameters of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite nanofibers is about 200 nm,the grains size is about 1-3 nm,and the fiber surface is rough.The electrochemical test results show that the heterojunction of the prepared Ni_(3)Fe/Ni_(4)S_(3)/Ni/C hybrid crystal composite nanofiber has synergistic effect with sulfide,and exhibits good electrocatalytic activity of water decomposition and OER in alkaline system.The OER electrocatalytic performance of Ni_(3)Fe/Ni_(4)S_(3)/Ni/C composite electrode prepared via a heat treatment at 1000℃process was tested in 1 mol/L KOH electrolytes.The results show that the overpotential is about 298 mV,the Tafel slope is about 74 mV?dec-1,and the surface resistance is about 1.69Ω·cm^(2),at the current density of 10 mA·cm^(-2).
基金supports provided by the National Natural Science Foundation of China(U21A2077,21971145,21871164)the Taishan Scholar Project Foundation of Shandong Province(ts20190908)+2 种基金the Natural Science Foundation of Shandong Province(ZR2021ZD05,ZR2019MB024)Young Scholars Program of Shandong University(2017WLJH15)and Anhui Kemi Machinery Technology Co.,Ltd.for providing a Teflon-lined stainless steel autoclave.
文摘Transition metal nitrides have attracted considerable attention as great potential anode materials due to their excellent metallic conductivity and high theoretical specific capacity.However,their cycling performance is impeded by their instability caused by the reaction mechanism.Herein,we report the engineering and synthesis of a novel hybrid architecture composed of MoO2.0N0.5 atomic nanoclusters bonded in nanosheets of N-doped carbon hierarchical hollow microspheres(MoO2.0N0.5/NC)as an anode material for sodium-ion batteries.The facile self-templating strategy for the synthesis of MoO2.0N0.5/NC involves chemical polymerization and subsequent one-step calcination treatments.The design is benefi-cial to improve the electrochemical kinetics,buffer the volume variation of electrodes during cycling,and provide more interfacial active sites for sodium uptake.Due to these unique structural and compositional merits,these MoO2.0N0.5/NC exhibits excellent sodium storage performance in terms of superior rate capability and stable long cycle life.The work shows a feasible and effective way to design novel host candidates and solve the long-term cycling stability issues for sodium-ion batteries.
基金Project supported by the Excellent Youth Project of Yunnan Province Applied Basic Research Project(2019FI001)the National Natural Science Foundation of China(61775187,61965012,12064022)the Key Project of Yunnan Provincial Natural Science Foundation(202101AT070126)。
文摘Red emitting phosphors play a significant role in accelerating the improvement of illumination quality for white light emitting diodes(WLEDs).In this work,by using solid-state reaction method,an efficient novel Ba_(2)LuNbO_(6):Eu^(3+)phosphor with double-perovskite structure was successfully prepared.Here,a series of Ba_(2)LuNbO_(6):Eu^(3+)red phosphors can be efficiently pumped by the near-ultraviolet(UV)light and then present high-brightness at orange emission(598 nm,~5D_(0)→~7 F_(1))and red emission(610 nm,~5D_(0)→~7 F_(2)).The ratio values of 610 to 598 nm in Ba_(2)LuNbO_(6):Eu^(3+)phosphors exceed 1 when the content of Eu^(3+)is larger than 0.4 mol,because the occupation of Eu^(3+)ions is changed from Lu^(3+)ions with symmetric sites to Ba^(2+)ions with asymmetric sites.Besides,the optimized concentration of Eu^(3+)at the~5D_(0)→~7 F_(2)transitions is obtained when x=1,indicating that there is non-concentration quenching in Ba_(2)LuNbO_(6):Eu^(3+)phosphors.Moreover,the CIE chromaticity coordinates of Ba_(2)LuNbO_(6):Eu^(3+)was calculated to be(0.587,0.361),the color purity was calculated to be 72.26%and internal quenching efficiency(IQE)was measured to be 67%.Finally,the thermal stability of Ba_(2)LuNbO_(6):Eu^(3+)phosphors was also studied.Our work demonstrates that the novel double-perovskite red-emitting Ba_(2)LuNbO_(6):Eu^(3+)phosphors are prospective red emitting elements for WLEDs applications.
基金supported by the National Natural Science Foundation of China(11572057)the School Foundation of Chengdu University(2080516030)~~
文摘In the present study,porous bulk palladium samples were prepared by sodium chloride salt powder spacer incorporation and removal combined with dealloying.The obtained porous Pd bulks were characterized by X‐ray diffraction,field‐emission scanning electron microscopy and N2adsorption isotherm measurements.The prepared porous Pd bulk samples showed a hierarchical pore structure,a high porosity of^88%,a high surface area of^54m2/g,and a compression strength of^0.5MPa.Electrochemical measurements were performed to evaluate the electrocatalytic properties of the porous Pd bulk samples,revealing their effectiveness for ethanol oxidation.
