Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purificatio...Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purification processes in modern industries.This study investigated the enhanced kinetic separatio n of target metal ions from complex aqueous solutio ns at a liquid-liquid interface,focusing on the presence of coexisting salt cations.Employing a typical thin-layer organic oil film(TOOF)extraction as a model system,the research examines how background Al^(3+)ions influence the mass transfer and separation of ions.Notably,the co ncentration of Al^(3+)ions affects both the distribution of Er^(3+)ions at the oil-water interface and the arrangement and orientation of P507 extractant molecules through the formation of unique hydrogen-bonding interactions.These interactions influence the selectivity of mass transfer,facilitating the separation of Er^(3+)from Al^(3+)ions.Specifically,the hydration shell of Er^(3+)ions is disrupted due to the strong hydration capability of coexisting Al^(3+)ions,leading to a higher interfacial concentration of Er^(3+)ions and a more ordered interfacial orientation of P507 molecules.At lower concentrations of Al^(3+)ions,the diffusion rate of Er^(3+)ions near the interface is high,enhancing the sepa ration perfo rmance of these ions.In contrast,at higher concentrations of Al^(3+)ions,the competitive hydration by Al^(3+)ions increases,and the interfacial concentration of Er^(3+)ions decreases due to enhanced diffusion resistance,resulting in poorer separation performance.Furthermore,a thinner membrane is more effective than a thicker one in enriching target Er^(3+)ions at the interface and achieving an ordered interfacial orientation of P507 molecules,thereby enhancing the separation coefficient(β_(Er/Al)).This work provides novel insights into the behaviors of ions and extractants at oil-wate r interface and the kinetic separation selectivity under varying concentrations of coexisting salt cations.展开更多
The flotation separation of cassiterite and dravite was realized using lead complexes of benzohydroxamic acid(Pb-BHA)as a collector and sodium fluosilicate(SF)as a depressant.Zeta potential tests confirmed that SF ena...The flotation separation of cassiterite and dravite was realized using lead complexes of benzohydroxamic acid(Pb-BHA)as a collector and sodium fluosilicate(SF)as a depressant.Zeta potential tests confirmed that SF enabled the selective depression of dravite.The results of Fourier transform infrared(FTIR)spectroscopy analysis demonstrated that hydroxyl-containing groups in the hydrolysis products of SF selectively chemisorbed on the surface of dravite.X-ray photoelectron spectroscopy(XPS)analysis results further demonstrated the strong chemisorption of SF hydrolysis products(F-containing groups and hydroxyl-containing groups)on dravite(Mg sites).Consequently,the adsorption of Pb-BHA on dravite was selectively prevented.Based on the results,a selective depression model of SF on cassiterite and dravite was proposed.展开更多
A robust spontaneous exchange bias effect after zero-field cooling was observed in Co_(2)Sn_(1-x)Cr_(x)O_(4)system,which was driven by the transition from superspin-glass to superferromagnetic domain embedded in the f...A robust spontaneous exchange bias effect after zero-field cooling was observed in Co_(2)Sn_(1-x)Cr_(x)O_(4)system,which was driven by the transition from superspin-glass to superferromagnetic domain embedded in the ferrimagnetic matrix.Additionally,the exchange bias effect is gradually pronounced with the positive increase in the cooling field,known as the conventional exchange bias effect.However,as the cooling field gradually decreases and transits from positive to negative,the exchange bias effect can robustly remain positive in the low-negative-field region until the cooling field increases to be sufficiently large in the negative direction.展开更多
This paper examines a model that combines vortex generators and leading-edge tubercles for controlling the laminar separation bubble(LSB)over an airfoil at low Reynolds numbers(Re).This new concept of passive flow con...This paper examines a model that combines vortex generators and leading-edge tubercles for controlling the laminar separation bubble(LSB)over an airfoil at low Reynolds numbers(Re).This new concept of passive flow control technique utilizing a tubercle and vortex generator(VG)close to the leading edge was analyzed numerically for a NACA0015 airfoil.In this study,the Shear Stress Transport(SST)turbulence model was employed in the numerical modelling.Numerical modelling was completed using the ANSYS-Fluent 18.2 solver.Analyses were conducted to investigate the flow pattern and understand the underlying LSB control phenomena that enabled the new passive flow control method to provide this significant performance benefit.The findings indicated that the new concept of passive flow control technique suppressed the formation of an LSB at the suction surface of the NACA0015 airfoil,resulting in a higher lift coefficient and improved aerodynamic performance.Improvements in LSB dynamics and aerodynamic performance through the passive flow control method lead to increased energy output and enhanced stability.展开更多
This paper demonstrates the strategic molecular design of functional polymer monoliths comprised of mesoporous fibers with stimuli-responsive Joule-heating properties for the rapid and efficient recovery of viscous fu...This paper demonstrates the strategic molecular design of functional polymer monoliths comprised of mesoporous fibers with stimuli-responsive Joule-heating properties for the rapid and efficient recovery of viscous fuel oil from water.The mesoporous fibers were composed of carefully selected monomers,which spontaneously entangled with each other to form a spongy monolith in a one-pot synthesis process.The subsequent addition of polypyrrole nanoparticles to the polymer produced superwettable intertwined fibers with strain-responsive conductivity,allowing the monolith to be used as a compressible,fibrous,and porous adsorbent with a high-flux separation capability and a tunable electrical heating effect.This adsorbent was demonstrated to successfully separate different types of low-viscosity oil from water in a continuous,highly efficient process.It also induced a rapid increase in the temperature during the recovery of marine fuel oil(MFO380),with a minimal compression of 3%under an external voltage.The proposed adsorbent can thus be used for the effective recovery of various fuel oils and improved further by incorporating other synergistic components for various water-treatment systems.展开更多
Surface pretreatment can change the surface properties of minerals,placing them in either a favorable or an unfavorable state for flotation.To solve the separation problem associated with magnesite and dolomite,surfac...Surface pretreatment can change the surface properties of minerals,placing them in either a favorable or an unfavorable state for flotation.To solve the separation problem associated with magnesite and dolomite,surface pretreatment experiments with citric acid,tartaric acid,and tannic acid(TA)on magnesite and dolomite as well as flotation experiments on pretreated samples were performed in this study.Experimental results demonstrated that when citric acid and tartaric acid are used for surface pretreatment,the separation effect of magnesite and dolomite is poor.However,when TA is used,the separation effect of magnesite and dolomite improves.SEM and BET analysis indicated that surface pretreatment with TA changes the surface morphology of the two minerals,resulting in additional concave pores on the dolomite surface,and a significant increase in pore size and specific surface area.The adsorption quantity test and contact angle measurement demonstrated that after surface pretreatment with TA,the magnesite adsorption capacity on sodium oleate(NaOL)slightly decreases and the dolomite adsorption capacity on NaOL considerably decreases.XPS detection concluded that the surface pretreatment of TA on the magnesite surface mainly relies on physical adsorption with weak adsorption ability and poor ability to act on Mg sites.The TA surface pretreatment action on the dolomite surface is mainly through chemical adsorption,and it is strongly and selectively adsorbed on the Ca site of dolomite through O.Actual ore rough selection experiments reveal that TA pretreatment successfully removes dolomite from magnesite,resulting in a high-quality magnesite concentrate characterized by a MgO grade of 45.49%and a CaO grade of 0.75%.展开更多
Selective separation of phenanthrene(PHE)from aromatic isomer mixtures poses a significant challenge in industry due to the similar physical properties of PHE and its isomer anthracene(ANT).Herein,we report the self-a...Selective separation of phenanthrene(PHE)from aromatic isomer mixtures poses a significant challenge in industry due to the similar physical properties of PHE and its isomer anthracene(ANT).Herein,we report the self-assembly of a water-soluble Pd_(2)L_(2) cage 1 with a large hydrophobic cavity,formed from novel macrocyclic ligands(L)and cis-Pd(Ⅱ).Cage 1 can selectively encapsulate PHE instead of ANT.Based on host-vip recognition followed by extraction,we achieve a remarkable 99%purity of PHE separation from an equimolar mixture of PHE and ANT using cage 1 in aqueous solution.Importantly,the separation performance of PHE using cage 1 remains unaffected even after five extraction cycles,demonstrating its robustness.This work highlights the potential of supramolecular cages for efficient and cost-effective PHE separation from the isomer ANT in aqueous solutions using such promising host-vip strategy.展开更多
TiAl alloys with the(α2+γ)lamellar structure are highly valued for their excellent high-temperature strength and creep resistance.Understanding the formation mechanism of the lamellar structure is crucial for tuning...TiAl alloys with the(α2+γ)lamellar structure are highly valued for their excellent high-temperature strength and creep resistance.Understanding the formation mechanism of the lamellar structure is crucial for tuning the microstructure and properties.This work investigates the formation of lamellar structure in Ti-48AI-7Nb-2.5V-1Cr alloy,revealing the presence of hcp-based long-period superstructure(hcp-LPS)as a metastable phase during lamellar formation.The identification of hcp-LPS demonstrates that the necessary solute enrichment for the formation ofγlamellae occurs on the hexagonalαmatrix,implying that phase separation ofα→Al-richαlamellae+Al-depletedαlamellae is the first step of lamellar formation.Once phase separation is completed,all subsequent phase transitions occur within the Al-richαlamellae.Additionally,the formation of twin lamellae is further discussed.The formation of the twin lamellae occurs sequentially.Pre-existing lamella promotes the formation of later lamella by inducing so-lute enrichment in its surrounding region,and then the successive slip of Shockley partial dislocations with opposite Burgers vectors ensures special stacking of later lamellae.These findings not only con-tribute to the fundamental understanding of spinodal mechanisms in hexagonal crystals,but also provide novel insights into the formation of twin lamellae.展开更多
Due to complex ion-ion and ion-membrane interactions, creating innovative membrane structures to acquire favorable ion mixing effect and high separation performance remains a big challenge. Herein, we design covalent ...Due to complex ion-ion and ion-membrane interactions, creating innovative membrane structures to acquire favorable ion mixing effect and high separation performance remains a big challenge. Herein, we design covalent organic framework(COF) scaffold membrane with gate-lane nanostructure for efficient Li^(+)/Mg^(2+) separation. COF nanosheets, serving as the scaffold, are intercalated by polyethyleneimine(PEI) to form the permeating layer. Subsequently, PEI on the surface reacts with 1,4-phenylene diisocyanate to form the polyurea gating layer. The gating layer, bearing tailored smaller pore size,affords high rejection to co-ions(Mg^(2+)) and thus high Li^(+)/Mg^(2+) selectivity. The permeating layer, with asymmetric charge and spatial nanostructure for creating individual lanes of Li^(+) and Cl~-, facilitates Li^(+) transport and thus high Li^(+) permeability. The optimum COF scaffold membrane exhibits the permeance of 11.5 L m^(-2) h^(-1)/bar^(-1) and true selectivity of 231.9 with Li^(+) enrichment of 120.2% at the Mg^(2+)/Li^(+) mass ratio of 50, exceeding the ideal selectivity of 80.5 and outperforming all ever-reported positively charged nanofiltration membranes. Our work may stimulate the further thinking about how to design the hierarchical membrane structure to achieve favorable ion mixing effect and break the membrane permeability-selectivity trade-off in chemical separations.展开更多
Spin-density(charge)separation,marked by distinct propagation velocities of spin and density excitations,epitomizes strong correlations,historically confined to one-dimensional(1D)systems.The recent experimental work ...Spin-density(charge)separation,marked by distinct propagation velocities of spin and density excitations,epitomizes strong correlations,historically confined to one-dimensional(1D)systems.The recent experimental work of Dhar et al(2025 Nature 64253),using a weakly interacting 3D Bose-Einstein condensate of^(133)Cs atoms confined in a 2D optical lattice to realize spin-density separation and demonstrate boson anyonization,motivates a deeper exploration into how dimensionality and interactions govern quantum correlations.In this work,we investigate this in two-component bosonic mixtures with finite-range interactions,probing 1D and 3D dynamics.Using path integral effective field theory within the one-loop approximation,we derive analytical expressions for zero-temperature ground-state energy and quantum depletion,seamlessly recovering contact interaction results in the contact limit.By crafting an effective action for decoupled density and spin modes,we compute dynamic structure factors(DSFs),revealing how finite-range interactions sculpt spin-density separation.A pivotal finding is the dimensionality-driven divergence in DSF peak dynamics:in 1D,peaks ascend to higher frequencies with increasing interaction strength,yielding sharp responses;in 3D,peaks descend to lower frequencies,with broader density wave profiles.These insights highlight dimensionality's critical role in collective excitations and provide a robust theoretical blueprint for probing interaction-driven quantum phenomena via Bragg spectroscopy,paving new pathways for the exploration of dimensionally tuned quantum correlations in ultracold quantum gases.展开更多
Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms lig...Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms ligand bonds or hydrogen bonds with sulfur ions in lithium polysulfides(LiPSs),thus inhibiting the shuttle effect.Electrochemical analyses demonstrated that lithium‑sulfur(Li‑S)batteries employing the NH2‑SS interlayer exhibited discharge specific capacities of 1048 and 789 mAh·g^(-1) at 0.2C and 2C,respectively,and even at 4C,the initial discharge specific capacity remained at 590 mAh·g^(-1),outperforming the Li‑S battery with unmodified SS as the interlayer.展开更多
Covalent organic skeletons(COFs)have been widely used in gas separation due to their excellent pore structure,high crystallinity,and high specific surface area.In this work,Dha Tab-COF was synthesized by solvothermal ...Covalent organic skeletons(COFs)have been widely used in gas separation due to their excellent pore structure,high crystallinity,and high specific surface area.In this work,Dha Tab-COF was synthesized by solvothermal method and filled in polyether block polyamide(PEBAX)to form mixed matrix membranes(MMMs).Various characterization methods such as Fourier transform infrared spectroscopy(FT-IR),Xray photoelectron spectroscopy(XPS),scanning electron microscopy(SEM)and X-ray diffractometry(XRD)were used to characterize the structure of Dha Tab-COF as well as the MMMs.The effects of operating pressure,operating temperature and the content of Dha Tab-COF particles on the CO_(2)/CH_(4)separation performance of the membranes were investigated.The best separation performance with a CO_(2)permeability of 295.8 barrer(1 barrer=7.52×10^(-18)m^(3)·(STP)·m^(-2)·m·s^(-1)·Pa^(-1))and a CO_(2)/CH_(4)selectivity of 21.6 was achieved when the Dha Tab-COF content is 2%(mass),which were 45.7%and 108.1%higher than that of the pure PEBAX membrane,respectively.展开更多
The in-flight heating process of cerium dioxide(CeO_(2))powders was investigated through experiments and numerical simulations.In the experiment,CeO_(2)powder(average size of 30μm)was injected into radio-frequency(RF...The in-flight heating process of cerium dioxide(CeO_(2))powders was investigated through experiments and numerical simulations.In the experiment,CeO_(2)powder(average size of 30μm)was injected into radio-frequency(RF)argon plasma,and the temperatures were measured using a DPV-2000 monitor.A model combining the electromagnetism,thermal flow,and heat transfer characteristics of powder during in-flight heating in argon plasma was proposed.The melting processes of CeO_(2)powders of different diameters,with and without thermal resistance effect,were investigated.Results show that the heating process of CeO_(2)powder particles consists of three main stages,one of which is relevant to a dimensionless parameter known as the Biot number.When the Biot value≥0.1,thermal resistance increases significantly,especially for the larger powders.The predicted temperature of the particles at the outlet(1800–2880 K)is in good agreement with the experimental result.展开更多
Agglomeration supports the high-quality development of the manufacturing industry,and its associated resource and environmental effects play a crucial role in driving green economic development.Based on data from pref...Agglomeration supports the high-quality development of the manufacturing industry,and its associated resource and environmental effects play a crucial role in driving green economic development.Based on data from prefecture-level cities in China from 2005 to 2019,this study employs the inverse distance weighting method,the bivariate local indicator of spatial association model,the spatial Durbin model,and other techniques to explore the relationship between manufacturing agglomeration and PM_(2.5)concentrations,and to assess the impact of its manufacturing agglomeration.Four correlation patterns are observed:high-high,low-low,high-low,and low-high.Among these,high-high and low-low patterns dominate in terms of number of cities.These correlation patterns demonstrate strong temporal stability,with a clear“Matthew effect”.The effect of manufacturing agglomeration on PM_(2.5)levels is significantly negative and helps reduce concentrations regionally,indicating the need to further enhance agglomeration levels regionally.However,it can increase PM_(2.5)levels in neighboring areas due to a siphon effect,and the impact of varies across regions.Compared with levels in 2005-2013,the significance of the relationship between manufacturing agglomeration and PM_(2.5)weakened in the 2013-2019 period.Accordingly,this study proposes countermeasures and policy recommendations aimed at strengthening regional collaborative governance and inspiring differentiated agglomeration strategies to support sustainable economic development in China.展开更多
Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticle...Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticles were chlorinated by NaClO solution to get AgCl@SiO_(2)/CTS‑based chloramine nano‑hybrid materials,denoted as AgCl@SiO_(2)/CTS‑Cl.A transmission electron microscope was used to observe the morphology of the as‑prepared samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.At the same time,an X‑ray diffractometer and an infrared spectroscope were utilized to characterize their crystal and chemical structures.Besides,ζpotentials were measured to elucidate the surface modification of AgCl nanoparticles by—NH_(2),the antibacterial mechanism of AgCl@SiO_(2)/CTS‑Cl was investigated by scanning electron microscopy,and Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)were used as the to‑be‑tested strains to evaluate the antimicrobial activity of samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.Findings demonstrate that sample AgCl@SiO_(2)/CTS exhibits a chain‑like structure ascribed to the interaction between—NH_(2),and each AgCl@SiO_(2)/CTS hybrid nanoparticle contains several AgCl cores.In the meantime,sample AgCl@SiO_(2)/CTS‑Cl exhibits excellent antibacterial activity against E.coli and S.aureus,which is attributed to the synergistic antibacterial effect of Ag^(+)and Cl^(-).Sample AgCl@SiO_(2)/CTS‑Cl with a dosage of 640.00μg·mL^(-1) could completely kill the two kinds of tested bacteria in 12 h of incubation;it retains a high antibacterial efficiency even after 10 cycles of antibacterial tests.展开更多
Microporous polyimides(PIM-PIs)have emerged as promising high-performance membranes for gas separation.However,achieving an optimal balance between permeability and selectivity remains a major challenge.In this study,...Microporous polyimides(PIM-PIs)have emerged as promising high-performance membranes for gas separation.However,achieving an optimal balance between permeability and selectivity remains a major challenge.In this study,we designed and synthesized a series of PIM-PIs by combining rigid dianhydrides 9-bis(trifluoromethyl)-2,3,6,7-xanthenetetracarboxylic dianhydride(6FCDA)and 4,4′-(hexafluoroisopropylidene)diphthalic anhydride(6FDA)with contorted diamines,including 9,9-bis(4-aminophenyl)fluorene(FDA),9,9′-spirobifluorene-2,2′-diamine(SBFDA),and 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-5,5′-diamine-6,6′-diol(TSDA),to systematically elucidate the relationship between hierarchical microstructure and gas transport behavior.Comprehensive characterization revealed that the 6FCDA-based polymers exhibited a higher microporosity(V_(micro)/V_(total)up to 54.7%)and fractional free volume compared to their 6FDA counterparts.Gas permeation measurements showed that the 6FCDA/SBFDA membrane delivered a CO_(2)permeability of 386 Barrer and CO_(2)/CH_(4)selectivity of 30.2,exceeding the 2008 Robeson upper bound.Structure-property correlation analyses indicated that diffusion selectivity predominantly governed gas separation performance,with rigid,spirocyclic architectures suppressing chain packing to generate sub-5Åmicropores,as further validated by molecular simulations.The optimized 6FCDA/FDA membrane achieved a BET surface area of 423 m^(2)·g^(−1),while maintaining excellent mechanical strength and high thermal stability.This work establishes an effective monomer design strategy to overcome the permeability-selectivity trade-off through backbone rigidification,thereby advancing PIM-PIs for practical applications in natural gas purification and carbon capture.展开更多
The dependence of interface structure and mechanical properties on the modulation layer thickness of VN/TiN−Ni nano-multilayered films deposited on Si substrates using a reactive magnetron sputtering technique was sys...The dependence of interface structure and mechanical properties on the modulation layer thickness of VN/TiN−Ni nano-multilayered films deposited on Si substrates using a reactive magnetron sputtering technique was systematically investigated. The films were characterized using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, and nanoindentation. The results show that the TiN−Ni layer grows epitaxially on the VN layer, forming a coherent interface between the two sublayers. When the deposition time ratio of the two sublayers (TTiN−Ni꞉TVN) is 10꞉12, the films exhibit remarkable mechanical properties, with hardness, elastic modulus, and fracture toughness values of 25.9 GPa, 317 GPa, and 1.88 MPa·m^(1/2), respectively. Meanwhile, fracture toughness is improved by approximately 50% compared to the VN monolithic film. This enhancement is attributed to the coherent interface between the sublayers and the phase separation in the TiN−Ni layer.展开更多
Taking the view that pro-environmental behaviors can have spillover effects,this study examines how household waste separation(an environmental behavior with a high degree of difficulty)impacts consumers’water saving...Taking the view that pro-environmental behaviors can have spillover effects,this study examines how household waste separation(an environmental behavior with a high degree of difficulty)impacts consumers’water saving efforts(an environmental behavior with a low degree of difficulty).We assess the mediating effects of self-efficacy and ego depletion in this relationship and the moderating effect of the need for self-determination in the mediated relationships.The results show separating household waste significantly enhances consumers’water-saving efforts.Both self-efficacy and ego depletion partially mediate the relationship between household waste separation and efforts to reduce water consumption.Specifically,if consumers engage in pro environmental behaviors based on their internal,rather than external sense of moral identity,their sense of self-efficacy increases after separating household,which motivates them to engage in subsequent water-saving behaviors.In addition,consumers’sense of ego depletion declines when they engage in household waste separation,which increases subsequent water-saving behavior.Compared to low-level self-determination needs,high-level self-determination needs weaken the positive impact of household waste separation on consumers’perceived self-efficacy,but strengthens the negative impact of household waste separation on consumers’perceived ego depletion and promotes subsequent water-saving behavior.These findings suggest policymakers should pay attention to the spillover effects pro-environmental behaviors and use household waste separation policies to promote other pro-environmental behaviors such as reducing water consumption.展开更多
Rechargeable Zn/Sn-air batteries have received considerable attention as promising energy storage devices.However,the electrochemical performance of these batteries is significantly constrained by the sluggish electro...Rechargeable Zn/Sn-air batteries have received considerable attention as promising energy storage devices.However,the electrochemical performance of these batteries is significantly constrained by the sluggish electrocatalytic reaction kinetics at the cathode.The integration of light energy into Zn/Sn-air batteries is a promising strategy for enhancing their performance.However,the photothermal and photoelectric effects generate heat in the battery under prolonged solar irradiation,leading to air cathode instability.This paper presents the first design and synthesis of Ni_(2)-1,5-diamino-4,8-dihydroxyanthraquinone(Ni_(2)DDA),an electronically conductiveπ-d conjugated metal-organic framework(MOF).Ni_(2)DDA exhibits both photoelectric and photothermal effects,with an optical band gap of~1.14 eV.Under illumination,Ni_(2)DDA achieves excellent oxygen evolution reaction performance(with an overpotential of 245 mV vs.reversible hydrogen electrode at 10 mA cm^(−2))and photothermal stability.These properties result from the synergy between the photoelectric and photothermal effects of Ni_(2)DDA.Upon integration into Zn/Sn-air batteries,Ni_(2)DDA ensures excellent cycling stability under light and exhibits remarkable performance in high-temperature environments up to 80℃.This study experimentally confirms the stable operation of photo-assisted Zn/Sn-air batteries under high-temperature conditions for the first time and provides novel insights into the application of electronically conductive MOFs in photoelectrocatalysis and photothermal catalysis.展开更多
The efficient electrocatalytic oxidation of glycerol(GLY)is one of the most promising routes for the valorization of GLY.Doping has emerged as a powerful strategy to tailor the electrocatalytic performance of silver n...The efficient electrocatalytic oxidation of glycerol(GLY)is one of the most promising routes for the valorization of GLY.Doping has emerged as a powerful strategy to tailor the electrocatalytic performance of silver nanoclusters(Ag NCs),yet the effects of doping mode(surface vs.core)and the interface environment(e.g.,electrolyte concentration)on the electrocatalytic performance for Ag NCs toward GLY oxidation remain understood.In this work,surface-doped Ag_(4)M_(2)(SR)_(8) and core-doped Ag_(24)M(SR)_(18)(M=Ni,Pd,Pt;SR=SPhMe_(2))NCs were synthesized for electrocatalytic GLY oxidation.The results revealed a strong dependence of selectivity on doping mode and electrolyte concentration:under low KOH concentration,Pd-and Pt-doped Ag_(4)M_(2) NCs exhibited 100%selectivity toward oxalic acid(OA),whereas Pd-and Pt-doped Ag_(24)M NCs delivered>95%selectivity for formic acid(FA).In contrast,under high KOH concentration,Pd-and Pt-doped Ag_(4)M_(2) NCs gave rise to>80%FA,while Pd-and Pt-doped Ag_(24)M NCs produced>45%FA.Mechanism studies indicated that Ni doping predominantly enhanced catalytic activity via lowering the activation barrier of the initial reaction step(GLY→glyceraldehyde),whereas Pd and Pt doping modulated selectivity through reducing the energy barrier of the selective branch step(glyceric acid→OA,OA→FA).High KOH concentration promoted the oxidation by increasing the electrochemical active surface area and facilitating electron transfer of Ag NCs.This study provides clear guidance for designing high-performance Ag-based electrocatalysts for biomass valorization.展开更多
基金Project supported by the National Natural Science Foundation of China(52074031,51574213,51904027)the Fundamental Research Funds for the Central Universities of China(06500104)。
文摘Understanding the underlying mechanism that enhances the separation of specific target ions from complex background aqueous solutions is crucial for achieving controllable chemical reactions and industrial purification processes in modern industries.This study investigated the enhanced kinetic separatio n of target metal ions from complex aqueous solutio ns at a liquid-liquid interface,focusing on the presence of coexisting salt cations.Employing a typical thin-layer organic oil film(TOOF)extraction as a model system,the research examines how background Al^(3+)ions influence the mass transfer and separation of ions.Notably,the co ncentration of Al^(3+)ions affects both the distribution of Er^(3+)ions at the oil-water interface and the arrangement and orientation of P507 extractant molecules through the formation of unique hydrogen-bonding interactions.These interactions influence the selectivity of mass transfer,facilitating the separation of Er^(3+)from Al^(3+)ions.Specifically,the hydration shell of Er^(3+)ions is disrupted due to the strong hydration capability of coexisting Al^(3+)ions,leading to a higher interfacial concentration of Er^(3+)ions and a more ordered interfacial orientation of P507 molecules.At lower concentrations of Al^(3+)ions,the diffusion rate of Er^(3+)ions near the interface is high,enhancing the sepa ration perfo rmance of these ions.In contrast,at higher concentrations of Al^(3+)ions,the competitive hydration by Al^(3+)ions increases,and the interfacial concentration of Er^(3+)ions decreases due to enhanced diffusion resistance,resulting in poorer separation performance.Furthermore,a thinner membrane is more effective than a thicker one in enriching target Er^(3+)ions at the interface and achieving an ordered interfacial orientation of P507 molecules,thereby enhancing the separation coefficient(β_(Er/Al)).This work provides novel insights into the behaviors of ions and extractants at oil-wate r interface and the kinetic separation selectivity under varying concentrations of coexisting salt cations.
基金supported by the National Natural Science Foundation of China(No.52122406)the National Key Research Center and Development Program of the 14th Five-year Plan of China(Nos.2022YFC2905104,2022YFC2905105).
文摘The flotation separation of cassiterite and dravite was realized using lead complexes of benzohydroxamic acid(Pb-BHA)as a collector and sodium fluosilicate(SF)as a depressant.Zeta potential tests confirmed that SF enabled the selective depression of dravite.The results of Fourier transform infrared(FTIR)spectroscopy analysis demonstrated that hydroxyl-containing groups in the hydrolysis products of SF selectively chemisorbed on the surface of dravite.X-ray photoelectron spectroscopy(XPS)analysis results further demonstrated the strong chemisorption of SF hydrolysis products(F-containing groups and hydroxyl-containing groups)on dravite(Mg sites).Consequently,the adsorption of Pb-BHA on dravite was selectively prevented.Based on the results,a selective depression model of SF on cassiterite and dravite was proposed.
基金financially supported by the National Natural Science Foundation of China(Nos.11474111 and 11604281)the Young Elite Scientists Sponsorship Program by CAST(No.YESS20220618)the Hundreds of Talents program of Sun Yat-sen University(No.210192)
文摘A robust spontaneous exchange bias effect after zero-field cooling was observed in Co_(2)Sn_(1-x)Cr_(x)O_(4)system,which was driven by the transition from superspin-glass to superferromagnetic domain embedded in the ferrimagnetic matrix.Additionally,the exchange bias effect is gradually pronounced with the positive increase in the cooling field,known as the conventional exchange bias effect.However,as the cooling field gradually decreases and transits from positive to negative,the exchange bias effect can robustly remain positive in the low-negative-field region until the cooling field increases to be sufficiently large in the negative direction.
基金the Scientific Research Projects Unit of Erciyes University under contract no:FDS-2022-11532 and FOA-2025-14773.
文摘This paper examines a model that combines vortex generators and leading-edge tubercles for controlling the laminar separation bubble(LSB)over an airfoil at low Reynolds numbers(Re).This new concept of passive flow control technique utilizing a tubercle and vortex generator(VG)close to the leading edge was analyzed numerically for a NACA0015 airfoil.In this study,the Shear Stress Transport(SST)turbulence model was employed in the numerical modelling.Numerical modelling was completed using the ANSYS-Fluent 18.2 solver.Analyses were conducted to investigate the flow pattern and understand the underlying LSB control phenomena that enabled the new passive flow control method to provide this significant performance benefit.The findings indicated that the new concept of passive flow control technique suppressed the formation of an LSB at the suction surface of the NACA0015 airfoil,resulting in a higher lift coefficient and improved aerodynamic performance.Improvements in LSB dynamics and aerodynamic performance through the passive flow control method lead to increased energy output and enhanced stability.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(no.2022R1C1C1003149 and 2020R1A5A8018367)by the Korea Institute of Marine Science&Technology Promotion(KIMST)funded by the Ministry of Oceans and Fisheries,Korea(00254781)This research was alsosupported by Basic Science Research Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(no.RS-202400345266)。
文摘This paper demonstrates the strategic molecular design of functional polymer monoliths comprised of mesoporous fibers with stimuli-responsive Joule-heating properties for the rapid and efficient recovery of viscous fuel oil from water.The mesoporous fibers were composed of carefully selected monomers,which spontaneously entangled with each other to form a spongy monolith in a one-pot synthesis process.The subsequent addition of polypyrrole nanoparticles to the polymer produced superwettable intertwined fibers with strain-responsive conductivity,allowing the monolith to be used as a compressible,fibrous,and porous adsorbent with a high-flux separation capability and a tunable electrical heating effect.This adsorbent was demonstrated to successfully separate different types of low-viscosity oil from water in a continuous,highly efficient process.It also induced a rapid increase in the temperature during the recovery of marine fuel oil(MFO380),with a minimal compression of 3%under an external voltage.The proposed adsorbent can thus be used for the effective recovery of various fuel oils and improved further by incorporating other synergistic components for various water-treatment systems.
基金Project(BGRIMM-KJSKL-2024-07) supported by the Open Foundation of State Key Laboratory of Mineral Processing,ChinaProjects(52374259,52174239) supported by the National Natural Science Foundation of China。
文摘Surface pretreatment can change the surface properties of minerals,placing them in either a favorable or an unfavorable state for flotation.To solve the separation problem associated with magnesite and dolomite,surface pretreatment experiments with citric acid,tartaric acid,and tannic acid(TA)on magnesite and dolomite as well as flotation experiments on pretreated samples were performed in this study.Experimental results demonstrated that when citric acid and tartaric acid are used for surface pretreatment,the separation effect of magnesite and dolomite is poor.However,when TA is used,the separation effect of magnesite and dolomite improves.SEM and BET analysis indicated that surface pretreatment with TA changes the surface morphology of the two minerals,resulting in additional concave pores on the dolomite surface,and a significant increase in pore size and specific surface area.The adsorption quantity test and contact angle measurement demonstrated that after surface pretreatment with TA,the magnesite adsorption capacity on sodium oleate(NaOL)slightly decreases and the dolomite adsorption capacity on NaOL considerably decreases.XPS detection concluded that the surface pretreatment of TA on the magnesite surface mainly relies on physical adsorption with weak adsorption ability and poor ability to act on Mg sites.The TA surface pretreatment action on the dolomite surface is mainly through chemical adsorption,and it is strongly and selectively adsorbed on the Ca site of dolomite through O.Actual ore rough selection experiments reveal that TA pretreatment successfully removes dolomite from magnesite,resulting in a high-quality magnesite concentrate characterized by a MgO grade of 45.49%and a CaO grade of 0.75%.
基金supported by the National Key Research and Development Program of China(Nos.2022YFA1503300 and 2021YFA1500400)the National Natural Science Foundation of China(Nos.22171262,21825107 and 22171264)the Science Foundation of Fujian Province(Nos.2021J01516 and 2021J02016)。
文摘Selective separation of phenanthrene(PHE)from aromatic isomer mixtures poses a significant challenge in industry due to the similar physical properties of PHE and its isomer anthracene(ANT).Herein,we report the self-assembly of a water-soluble Pd_(2)L_(2) cage 1 with a large hydrophobic cavity,formed from novel macrocyclic ligands(L)and cis-Pd(Ⅱ).Cage 1 can selectively encapsulate PHE instead of ANT.Based on host-vip recognition followed by extraction,we achieve a remarkable 99%purity of PHE separation from an equimolar mixture of PHE and ANT using cage 1 in aqueous solution.Importantly,the separation performance of PHE using cage 1 remains unaffected even after five extraction cycles,demonstrating its robustness.This work highlights the potential of supramolecular cages for efficient and cost-effective PHE separation from the isomer ANT in aqueous solutions using such promising host-vip strategy.
基金supported by the National Science and Technology Major Project of China(No.J2019-VI-0011-0125)ND Basic Research Funds of China(No.G2022WD)Shaanxi Province Innovation Capability Support Program(No.2023-CX-TD-47).
文摘TiAl alloys with the(α2+γ)lamellar structure are highly valued for their excellent high-temperature strength and creep resistance.Understanding the formation mechanism of the lamellar structure is crucial for tuning the microstructure and properties.This work investigates the formation of lamellar structure in Ti-48AI-7Nb-2.5V-1Cr alloy,revealing the presence of hcp-based long-period superstructure(hcp-LPS)as a metastable phase during lamellar formation.The identification of hcp-LPS demonstrates that the necessary solute enrichment for the formation ofγlamellae occurs on the hexagonalαmatrix,implying that phase separation ofα→Al-richαlamellae+Al-depletedαlamellae is the first step of lamellar formation.Once phase separation is completed,all subsequent phase transitions occur within the Al-richαlamellae.Additionally,the formation of twin lamellae is further discussed.The formation of the twin lamellae occurs sequentially.Pre-existing lamella promotes the formation of later lamella by inducing so-lute enrichment in its surrounding region,and then the successive slip of Shockley partial dislocations with opposite Burgers vectors ensures special stacking of later lamellae.These findings not only con-tribute to the fundamental understanding of spinodal mechanisms in hexagonal crystals,but also provide novel insights into the formation of twin lamellae.
基金financial support from the National Natural Science Foundation of China (22338011, 22378299)Hainan Province Science and Technology Special Fund (ZDYF2025SHFZ025)+1 种基金Ningbo Key Research and Development Project (2022Z121)the China Postdoctoral Science Foundation (2025M771194)。
文摘Due to complex ion-ion and ion-membrane interactions, creating innovative membrane structures to acquire favorable ion mixing effect and high separation performance remains a big challenge. Herein, we design covalent organic framework(COF) scaffold membrane with gate-lane nanostructure for efficient Li^(+)/Mg^(2+) separation. COF nanosheets, serving as the scaffold, are intercalated by polyethyleneimine(PEI) to form the permeating layer. Subsequently, PEI on the surface reacts with 1,4-phenylene diisocyanate to form the polyurea gating layer. The gating layer, bearing tailored smaller pore size,affords high rejection to co-ions(Mg^(2+)) and thus high Li^(+)/Mg^(2+) selectivity. The permeating layer, with asymmetric charge and spatial nanostructure for creating individual lanes of Li^(+) and Cl~-, facilitates Li^(+) transport and thus high Li^(+) permeability. The optimum COF scaffold membrane exhibits the permeance of 11.5 L m^(-2) h^(-1)/bar^(-1) and true selectivity of 231.9 with Li^(+) enrichment of 120.2% at the Mg^(2+)/Li^(+) mass ratio of 50, exceeding the ideal selectivity of 80.5 and outperforming all ever-reported positively charged nanofiltration membranes. Our work may stimulate the further thinking about how to design the hierarchical membrane structure to achieve favorable ion mixing effect and break the membrane permeability-selectivity trade-off in chemical separations.
基金supported by the National Natural Science Foundation of China(Grant No.12574301)the Zhejiang Provincial Natural Science Foundation(Grant No.LZ25A040004)。
文摘Spin-density(charge)separation,marked by distinct propagation velocities of spin and density excitations,epitomizes strong correlations,historically confined to one-dimensional(1D)systems.The recent experimental work of Dhar et al(2025 Nature 64253),using a weakly interacting 3D Bose-Einstein condensate of^(133)Cs atoms confined in a 2D optical lattice to realize spin-density separation and demonstrate boson anyonization,motivates a deeper exploration into how dimensionality and interactions govern quantum correlations.In this work,we investigate this in two-component bosonic mixtures with finite-range interactions,probing 1D and 3D dynamics.Using path integral effective field theory within the one-loop approximation,we derive analytical expressions for zero-temperature ground-state energy and quantum depletion,seamlessly recovering contact interaction results in the contact limit.By crafting an effective action for decoupled density and spin modes,we compute dynamic structure factors(DSFs),revealing how finite-range interactions sculpt spin-density separation.A pivotal finding is the dimensionality-driven divergence in DSF peak dynamics:in 1D,peaks ascend to higher frequencies with increasing interaction strength,yielding sharp responses;in 3D,peaks descend to lower frequencies,with broader density wave profiles.These insights highlight dimensionality's critical role in collective excitations and provide a robust theoretical blueprint for probing interaction-driven quantum phenomena via Bragg spectroscopy,paving new pathways for the exploration of dimensionally tuned quantum correlations in ultracold quantum gases.
文摘Herein,3‑aminopropyltriethoxysilane(APTES)was used to modify F‑containing silica slag(SS)by simple grafting and served as a multifunctional barrier layer.The amino group(—NH2)in the amino‑modified SS(NH2‑SS)forms ligand bonds or hydrogen bonds with sulfur ions in lithium polysulfides(LiPSs),thus inhibiting the shuttle effect.Electrochemical analyses demonstrated that lithium‑sulfur(Li‑S)batteries employing the NH2‑SS interlayer exhibited discharge specific capacities of 1048 and 789 mAh·g^(-1) at 0.2C and 2C,respectively,and even at 4C,the initial discharge specific capacity remained at 590 mAh·g^(-1),outperforming the Li‑S battery with unmodified SS as the interlayer.
基金supported by the National Natural Science Foundation of China(No.22271022,No 22378327).
文摘Covalent organic skeletons(COFs)have been widely used in gas separation due to their excellent pore structure,high crystallinity,and high specific surface area.In this work,Dha Tab-COF was synthesized by solvothermal method and filled in polyether block polyamide(PEBAX)to form mixed matrix membranes(MMMs).Various characterization methods such as Fourier transform infrared spectroscopy(FT-IR),Xray photoelectron spectroscopy(XPS),scanning electron microscopy(SEM)and X-ray diffractometry(XRD)were used to characterize the structure of Dha Tab-COF as well as the MMMs.The effects of operating pressure,operating temperature and the content of Dha Tab-COF particles on the CO_(2)/CH_(4)separation performance of the membranes were investigated.The best separation performance with a CO_(2)permeability of 295.8 barrer(1 barrer=7.52×10^(-18)m^(3)·(STP)·m^(-2)·m·s^(-1)·Pa^(-1))and a CO_(2)/CH_(4)selectivity of 21.6 was achieved when the Dha Tab-COF content is 2%(mass),which were 45.7%and 108.1%higher than that of the pure PEBAX membrane,respectively.
基金National Natural Science Foundation of China(11875039)Shanxi Scholarship Council of China(2023-033)+2 种基金Fundamental Research Program of Shanxi Province(202303021221071)China Baowu Low Carbon Metallurgical Innovation Foundation(2022)2023 Anhui Major Industrial Innovation Plan Project。
文摘The in-flight heating process of cerium dioxide(CeO_(2))powders was investigated through experiments and numerical simulations.In the experiment,CeO_(2)powder(average size of 30μm)was injected into radio-frequency(RF)argon plasma,and the temperatures were measured using a DPV-2000 monitor.A model combining the electromagnetism,thermal flow,and heat transfer characteristics of powder during in-flight heating in argon plasma was proposed.The melting processes of CeO_(2)powders of different diameters,with and without thermal resistance effect,were investigated.Results show that the heating process of CeO_(2)powder particles consists of three main stages,one of which is relevant to a dimensionless parameter known as the Biot number.When the Biot value≥0.1,thermal resistance increases significantly,especially for the larger powders.The predicted temperature of the particles at the outlet(1800–2880 K)is in good agreement with the experimental result.
基金supported by the National Natural Science Foundation of China“Research on the Multi-scale Regional Industrial Spatial Evolution Mechanism,Resource and Environmental Effects,and Green Transformation in the Yellow River Basin”[Grant No.42371194]Taishan Scholar Foundation of Shandong Province[Grant Nos.tsqn202408148 and tstp20240821].
文摘Agglomeration supports the high-quality development of the manufacturing industry,and its associated resource and environmental effects play a crucial role in driving green economic development.Based on data from prefecture-level cities in China from 2005 to 2019,this study employs the inverse distance weighting method,the bivariate local indicator of spatial association model,the spatial Durbin model,and other techniques to explore the relationship between manufacturing agglomeration and PM_(2.5)concentrations,and to assess the impact of its manufacturing agglomeration.Four correlation patterns are observed:high-high,low-low,high-low,and low-high.Among these,high-high and low-low patterns dominate in terms of number of cities.These correlation patterns demonstrate strong temporal stability,with a clear“Matthew effect”.The effect of manufacturing agglomeration on PM_(2.5)levels is significantly negative and helps reduce concentrations regionally,indicating the need to further enhance agglomeration levels regionally.However,it can increase PM_(2.5)levels in neighboring areas due to a siphon effect,and the impact of varies across regions.Compared with levels in 2005-2013,the significance of the relationship between manufacturing agglomeration and PM_(2.5)weakened in the 2013-2019 period.Accordingly,this study proposes countermeasures and policy recommendations aimed at strengthening regional collaborative governance and inspiring differentiated agglomeration strategies to support sustainable economic development in China.
文摘Chitosan(CTS)was grafted onto the surface of amino‑functionalized silver chloride silicon dioxide(AgCl@SiO_(2)‑NH_(2))cores to obtain AgCl@SiO_(2)/CTS hybrid nanoparticles.The as‑obtained AgCl@SiO_(2)/CTS nanoparticles were chlorinated by NaClO solution to get AgCl@SiO_(2)/CTS‑based chloramine nano‑hybrid materials,denoted as AgCl@SiO_(2)/CTS‑Cl.A transmission electron microscope was used to observe the morphology of the as‑prepared samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.At the same time,an X‑ray diffractometer and an infrared spectroscope were utilized to characterize their crystal and chemical structures.Besides,ζpotentials were measured to elucidate the surface modification of AgCl nanoparticles by—NH_(2),the antibacterial mechanism of AgCl@SiO_(2)/CTS‑Cl was investigated by scanning electron microscopy,and Escherichia coli(E.coli)and Staphylococcus aureus(S.aureus)were used as the to‑be‑tested strains to evaluate the antimicrobial activity of samples AgCl@SiO_(2)/CTS and AgCl@SiO_(2)/CTS‑Cl.Findings demonstrate that sample AgCl@SiO_(2)/CTS exhibits a chain‑like structure ascribed to the interaction between—NH_(2),and each AgCl@SiO_(2)/CTS hybrid nanoparticle contains several AgCl cores.In the meantime,sample AgCl@SiO_(2)/CTS‑Cl exhibits excellent antibacterial activity against E.coli and S.aureus,which is attributed to the synergistic antibacterial effect of Ag^(+)and Cl^(-).Sample AgCl@SiO_(2)/CTS‑Cl with a dosage of 640.00μg·mL^(-1) could completely kill the two kinds of tested bacteria in 12 h of incubation;it retains a high antibacterial efficiency even after 10 cycles of antibacterial tests.
基金financially supported by the Sinopec Seed Program Project(No.223281)State Key Laboratory of Advanced Papermaking and Paper-based Materials(No.2024ZD06)+3 种基金Guangdong Basic and Applied Basic Research Foundation(Nos.2022A1515110543 and 2023A1515110170)the Natural Science Foundation of Guangdong Province(No.2024B1515040023)Guangjuyingcai program of Guangzhou(No.2024D03J0002)111 Project(No.B18023).
文摘Microporous polyimides(PIM-PIs)have emerged as promising high-performance membranes for gas separation.However,achieving an optimal balance between permeability and selectivity remains a major challenge.In this study,we designed and synthesized a series of PIM-PIs by combining rigid dianhydrides 9-bis(trifluoromethyl)-2,3,6,7-xanthenetetracarboxylic dianhydride(6FCDA)and 4,4′-(hexafluoroisopropylidene)diphthalic anhydride(6FDA)with contorted diamines,including 9,9-bis(4-aminophenyl)fluorene(FDA),9,9′-spirobifluorene-2,2′-diamine(SBFDA),and 3,3,3′,3′-tetramethyl-1,1′-spirobiindane-5,5′-diamine-6,6′-diol(TSDA),to systematically elucidate the relationship between hierarchical microstructure and gas transport behavior.Comprehensive characterization revealed that the 6FCDA-based polymers exhibited a higher microporosity(V_(micro)/V_(total)up to 54.7%)and fractional free volume compared to their 6FDA counterparts.Gas permeation measurements showed that the 6FCDA/SBFDA membrane delivered a CO_(2)permeability of 386 Barrer and CO_(2)/CH_(4)selectivity of 30.2,exceeding the 2008 Robeson upper bound.Structure-property correlation analyses indicated that diffusion selectivity predominantly governed gas separation performance,with rigid,spirocyclic architectures suppressing chain packing to generate sub-5Åmicropores,as further validated by molecular simulations.The optimized 6FCDA/FDA membrane achieved a BET surface area of 423 m^(2)·g^(−1),while maintaining excellent mechanical strength and high thermal stability.This work establishes an effective monomer design strategy to overcome the permeability-selectivity trade-off through backbone rigidification,thereby advancing PIM-PIs for practical applications in natural gas purification and carbon capture.
基金financially supported by the National Natural Science Foundation of China(No.51971148)the Key Project Foundation of Hanjiang Normal University,China(No.XJ2024A09)+1 种基金the Excellent Young and Middle-aged Science and Technology Innovation Team Project in Higher Education Institutions of Hubei Province,China(No.T2020024)the Shanghai Engineering Research Center of High-Performance Medical Device Materials,China(No.20DZ2255500)。
文摘The dependence of interface structure and mechanical properties on the modulation layer thickness of VN/TiN−Ni nano-multilayered films deposited on Si substrates using a reactive magnetron sputtering technique was systematically investigated. The films were characterized using X-ray diffraction, scanning electron microscopy, X-ray photoelectron spectroscopy, transmission electron microscopy, and nanoindentation. The results show that the TiN−Ni layer grows epitaxially on the VN layer, forming a coherent interface between the two sublayers. When the deposition time ratio of the two sublayers (TTiN−Ni꞉TVN) is 10꞉12, the films exhibit remarkable mechanical properties, with hardness, elastic modulus, and fracture toughness values of 25.9 GPa, 317 GPa, and 1.88 MPa·m^(1/2), respectively. Meanwhile, fracture toughness is improved by approximately 50% compared to the VN monolithic film. This enhancement is attributed to the coherent interface between the sublayers and the phase separation in the TiN−Ni layer.
基金supported by the National Social Science Fund of China[Grant No.25BGL131].
文摘Taking the view that pro-environmental behaviors can have spillover effects,this study examines how household waste separation(an environmental behavior with a high degree of difficulty)impacts consumers’water saving efforts(an environmental behavior with a low degree of difficulty).We assess the mediating effects of self-efficacy and ego depletion in this relationship and the moderating effect of the need for self-determination in the mediated relationships.The results show separating household waste significantly enhances consumers’water-saving efforts.Both self-efficacy and ego depletion partially mediate the relationship between household waste separation and efforts to reduce water consumption.Specifically,if consumers engage in pro environmental behaviors based on their internal,rather than external sense of moral identity,their sense of self-efficacy increases after separating household,which motivates them to engage in subsequent water-saving behaviors.In addition,consumers’sense of ego depletion declines when they engage in household waste separation,which increases subsequent water-saving behavior.Compared to low-level self-determination needs,high-level self-determination needs weaken the positive impact of household waste separation on consumers’perceived self-efficacy,but strengthens the negative impact of household waste separation on consumers’perceived ego depletion and promotes subsequent water-saving behavior.These findings suggest policymakers should pay attention to the spillover effects pro-environmental behaviors and use household waste separation policies to promote other pro-environmental behaviors such as reducing water consumption.
基金supported by the National Natural Science Foundation of China(No.62464010)Spring City Plan-Special Program for Young Talents(K202005007)+2 种基金Yunnan Talents Support Plan for Young Talents(XDYC-QNRC-2022-0482)Yunnan Local Colleges Applied Basic Research Projects(202101BA070001-138)Frontier Research Team of Kunming University 2023.
文摘Rechargeable Zn/Sn-air batteries have received considerable attention as promising energy storage devices.However,the electrochemical performance of these batteries is significantly constrained by the sluggish electrocatalytic reaction kinetics at the cathode.The integration of light energy into Zn/Sn-air batteries is a promising strategy for enhancing their performance.However,the photothermal and photoelectric effects generate heat in the battery under prolonged solar irradiation,leading to air cathode instability.This paper presents the first design and synthesis of Ni_(2)-1,5-diamino-4,8-dihydroxyanthraquinone(Ni_(2)DDA),an electronically conductiveπ-d conjugated metal-organic framework(MOF).Ni_(2)DDA exhibits both photoelectric and photothermal effects,with an optical band gap of~1.14 eV.Under illumination,Ni_(2)DDA achieves excellent oxygen evolution reaction performance(with an overpotential of 245 mV vs.reversible hydrogen electrode at 10 mA cm^(−2))and photothermal stability.These properties result from the synergy between the photoelectric and photothermal effects of Ni_(2)DDA.Upon integration into Zn/Sn-air batteries,Ni_(2)DDA ensures excellent cycling stability under light and exhibits remarkable performance in high-temperature environments up to 80℃.This study experimentally confirms the stable operation of photo-assisted Zn/Sn-air batteries under high-temperature conditions for the first time and provides novel insights into the application of electronically conductive MOFs in photoelectrocatalysis and photothermal catalysis.
基金support from the Jiangsu Natural Science Foundation of China(BK20230329)the National Natural Science Foundation of China(22401147,22361132540,and 22178161)the Russian Science Foundation(23-73-30007).
文摘The efficient electrocatalytic oxidation of glycerol(GLY)is one of the most promising routes for the valorization of GLY.Doping has emerged as a powerful strategy to tailor the electrocatalytic performance of silver nanoclusters(Ag NCs),yet the effects of doping mode(surface vs.core)and the interface environment(e.g.,electrolyte concentration)on the electrocatalytic performance for Ag NCs toward GLY oxidation remain understood.In this work,surface-doped Ag_(4)M_(2)(SR)_(8) and core-doped Ag_(24)M(SR)_(18)(M=Ni,Pd,Pt;SR=SPhMe_(2))NCs were synthesized for electrocatalytic GLY oxidation.The results revealed a strong dependence of selectivity on doping mode and electrolyte concentration:under low KOH concentration,Pd-and Pt-doped Ag_(4)M_(2) NCs exhibited 100%selectivity toward oxalic acid(OA),whereas Pd-and Pt-doped Ag_(24)M NCs delivered>95%selectivity for formic acid(FA).In contrast,under high KOH concentration,Pd-and Pt-doped Ag_(4)M_(2) NCs gave rise to>80%FA,while Pd-and Pt-doped Ag_(24)M NCs produced>45%FA.Mechanism studies indicated that Ni doping predominantly enhanced catalytic activity via lowering the activation barrier of the initial reaction step(GLY→glyceraldehyde),whereas Pd and Pt doping modulated selectivity through reducing the energy barrier of the selective branch step(glyceric acid→OA,OA→FA).High KOH concentration promoted the oxidation by increasing the electrochemical active surface area and facilitating electron transfer of Ag NCs.This study provides clear guidance for designing high-performance Ag-based electrocatalysts for biomass valorization.
