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
The existence of absorption and reflection of light underwater leads to problems such as color distortion and blue-green bias in underwater images.In this study,a depthwise separable convolution-based generative adver...The existence of absorption and reflection of light underwater leads to problems such as color distortion and blue-green bias in underwater images.In this study,a depthwise separable convolution-based generative adversarial network(GAN)algorithm was proposed.Taking GAN as the basic framework,it combined a depthwise separable convolution module,attention mechanism,and reconstructed convolution module to realize the enhancement of underwater degraded images.Multi-scale features were captured by the depthwise separable convolution module,and the attention mechanism was utilized to enhance attention to important features.The reconstructed convolution module further extracts and fuses local and global features.Experimental results showed that the algorithm performs well in improving the color bias and blurring of underwater images,with PSNR reaching 27.835,SSIM reaching 0.883,UIQM reaching 3.205,and UCIQE reaching 0.713.The enhanced image outperforms the comparison algorithm in both subjective and objective metrics.展开更多
With the legislative development,the organic and inorganic composition separation has become the primary requirement for sewer sediment disposal,however the relevant technology has been rarely reported and the driving...With the legislative development,the organic and inorganic composition separation has become the primary requirement for sewer sediment disposal,however the relevant technology has been rarely reported and the driving mechanism was still unclear.In this study,direct disintegration of biopolymers and indirect broken of connection point were investigated on the hydrolysis and component separation.Three typical sewer sediment treatment approaches,i.e.,alkaline,thermal and cation exchange treatments were proposed,which represented the hydrolysis-driving forces of chemical hydrolysis,physical hydrolysis and innovative cation bridging break-age.The results showed that the organic and inorganic separation rates of sewer sediment driven by alkaline,thermal and cation exchange treatments reached 21.26%,23.80%,and 19.56%-48.0%,respectively,compared to 4.43%in control.The secondary structure of proteins was disrupted,transitioning from𝛼α-helix to𝛽β-turn and random coil.Meanwhile,much biopolymers were released from solid to the liquid phase.From thermody-namic perspective,sewer sediment deposition was controlled by short-range interfacial interactions described by extended Derjaguin-Landau-Verwey-Overbeek theory.Additionally,the separation of organic and inorganic components was positively correlated with the thermodynamic parameters(Corr=0.87),highlighted the robust-ness of various driving forces.And the flocculation energy barriers were 2.40(alkaline),1.60 times(thermal),and 4.02–4.97 times(cation exchange)compared to control group.The findings revealed the contrition differ-ence of direct disintegration of gelatinous biopolymers and indirect breakage of composition connection sites in sediment composition separation,filling the critical gaps in understanding the specific mechanisms of sediment biopolymer disintegration and intermolecular connection breakage.展开更多
Lithium(Li)dendrites,resulting from poor ion desolvation and transport behavior at the anode/electrolyte interface during electrodeposition,severely impede the practicality of Li metal anodes.Inspired by the transmemb...Lithium(Li)dendrites,resulting from poor ion desolvation and transport behavior at the anode/electrolyte interface during electrodeposition,severely impede the practicality of Li metal anodes.Inspired by the transmembrane cascade transport mechanism of biological ion pumps,we design a biomimetic dual-cascade separator(BDS)based on gradient pore core–shell Gd_(2)O_(3)@ZIF-7 nanoparticles to stabilize Li metal anodes.The mesoporous Gd_(2)O_(3)core,via Lewis acidic surface,weakens Li^(+) -solvent interactions,thereby reconstructing the solvation structure and achieving pre-desolvation.The microporous ZIF-7 shell then promotes final desolvation through strong confinement effect and N-rich site coordination,while its nanochannels homogenize Li^(+) transport.This synergistic meso/microporous gradient creates a unique dual-cascade effect for ion desolvation and transport.Consequently,BDS achieves a low desolvation energy barrier,a high Li^(+) transference number(0.71),and dendrite-free Li deposition.The average Coulombic efficiency rises from 72.7%to 98.4%,the cycling performance of the Li||Li symmetrical cell improves by 3.2 times,and the capacity retention of LiFePO_4(LFP)||Li full cell increases from 38.3%to73.4%after 500 cycles.This work offers a novel separator design concept,deepens Li deposition understanding,and guides separators from passive protection to active regulation.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
The efficient flotation separation of rare earth elements(REEs)from gangue minerals is crucial in mineral processing.This study synthesized a quaternary ammonium salt ionic liquid collector,tetrabutylammonium salicylh...The efficient flotation separation of rare earth elements(REEs)from gangue minerals is crucial in mineral processing.This study synthesized a quaternary ammonium salt ionic liquid collector,tetrabutylammonium salicylhydroxamate(T-S),and investigated its performance in separating bastnaesite and fluorite.T-S was synthesized from salicylhydroxamic acid(SHA)and tetrabutylammonium chloride(TBAC),and its molecular structure was characterized using Fourier transform infrared(FTIR)spectroscopy.Microflotation tests indicate that T-S outperforms SHA and TBAC in both collecting ability and selectivity for bastnaesite.Adsorption,zeta potential,and infrared spectroscopy measurements reveal that T-S exhibits stronger adsorption on bastnaesite compared to SHA and TBAC.X-ray photoelectron spectroscopy(XPS)and molecular dynamics simulations(MDS)results confirm that chemical adsorption occurs between Ce on the bastnaesite surface and the-C(=O)NHOH groups of T-S.Moreover,the interaction between T-S and the bastnaesite surface is stronger than that with the fluorite surface.This work provides valuable insights for designing ionic liquid collectors for the flotation separation of bastnaesite and fluorite.展开更多
Bayan Obo rare earth mine is the largest light rare earth resource worldwide,primarily extracts rare earth elements(REEs)from mixed RE concentrates with bastnaesite and monazite.Nevertheless,the adoption of the concen...Bayan Obo rare earth mine is the largest light rare earth resource worldwide,primarily extracts rare earth elements(REEs)from mixed RE concentrates with bastnaesite and monazite.Nevertheless,the adoption of the concentrated sulfuric acid roasting metallurgical process has resulted in damage to the environment.Therefore,this paper adopted the method of selective mineral phase transformation(MPT)followed by enhanced micro-flotation.By determining the optimal MPT co nditions,the flotation recovery of bastnaesite-roasted products by the collector(phthalic acid,PA)is improved,and the enhanced separation of bastnaesite with monazite is realized.The results show that with the increase of roasting temperature and time,the bastnaesite decomposition product is CeOF and monazite does not change significantly.Subsequent micro-flotation exhibits a gradual decline in the PA consumption of bastnaesiteroasted products,while the flotation recovery of monazite-roasted products remains poor.The artificial mixed ore experiments result in a CeOF foam product with a content of 94.14%and a recovery of 85.80%,and a monazite tank product with a content of 73.53%and a recovery of 87.87%.Compared with the preroasting ore,the surface and interior of bastnaesite-roasted products develop numerous cracks and porosities,and no obvious structural damage is observed in monazite-roasted particles.As the roasting temperature increases,the mineral particles undergo recrystallization or closure,reducing the specific surface area of bastnaesite-roasted products and enhancing hydrophobicity,leading to diminished PA consumption.Fourier transform infrared and other flotation-relation tests show that PA is chemisorbed on the surface of CeOF.The MPT conditions are optimized in this study,which provides a reference for further advancing the efficient separation of bastnaesite and monazite.展开更多
Lithium-sulfur batteries(LSBs)represent a next-generation energy storage technology,but widespread applications are restricted by the shuttle of lithium polysulfides(LiPSs).The rational design of separators has been d...Lithium-sulfur batteries(LSBs)represent a next-generation energy storage technology,but widespread applications are restricted by the shuttle of lithium polysulfides(LiPSs).The rational design of separators has been demonstrated to be one of the most efficient and cost-effective strategies to curb the shuttle effect,and tremendous research progress has been achieved.The efficiency of a separator depends on its interaction with LiPSs,which is governed by the surface energy and binding strength.Despite several review works that have been reported to advance the separators,most of them primarily focus on active material innovation and construction.The most crucial issues of surface binding energy have not been systematically reviewed,limiting the precise design of efficient separators.In this review,fundamentals related to surface energy and binding interactions with LiPSs are comprehensively analyzed and discussed.With surface binding and energy main lines,the advancements in separator engineering strategies are elaborately summarized and discussed.Moreover,techniques for evaluating affinity to LiPSs are thoroughly analyzed to avoid any ambiguities in measurement.Based on the research context,valuable research directions are suggested to construct efficient separators.This work provides guidelines to regulate the surface binding and energy of separators for high-performance LSBs.展开更多
Developing advanced polymeric materials with enhanced mechanical properties and functionalities has been a long-standing goal in materials science.Recently,supramolecular polymeric materials (SPMs) have drawn increase...Developing advanced polymeric materials with enhanced mechanical properties and functionalities has been a long-standing goal in materials science.Recently,supramolecular polymeric materials (SPMs) have drawn increased attention due to their unique properties and potential applications in self-healing,shape memory,sensors,and flexible electronics.Here,we develop an ionic cluster-optimized microphase separation strategy to enhance the toughening and energy dissipation capabilities of polydisulfide-based supramolecular polymers.The mechanical properties,including Young’s modulus and toughness,are significantly improved by integrating the quadruple H-bonding 2-ureido-4-pyrimidone (UPy) induced microphase separation with iron(Ⅲ)-to-carboxylate ionic clusters.By combining established chemical approaches with adjustable polymer phase ratios,it is revealed that the synergistic effect of these factors expands the interchain spacing,facilitates the formation of microphase domains,and enhances the tolerance of polythioctic acid-based polymers to external mechanical and thermal stimuli,meeting the practical requirements for industrial plastic applications.Moreover,the UPy-functionalized polymers incorporating iron carboxylate clusters exhibit good one-way shape memory behavior with practical applicability at a relatively low recovery temperature.Our work demonstrates a novel strategy for constructing industrially viable shape memory dynamic SPMs and paves the way for future innovations in developing SPMs.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
Traditional fluorination strategies have attracted significant attention due to their ability to construct a fluorine-rich solid-electrolyte interphase(SEI)at the anode-electrolyte interface.However,the inhomogeneous ...Traditional fluorination strategies have attracted significant attention due to their ability to construct a fluorine-rich solid-electrolyte interphase(SEI)at the anode-electrolyte interface.However,the inhomogeneous distribution of LiF within the SEI layer remains a critical challenge that hinders the effective suppression of lithium dendrite growth.This work explores the synergy between HDBDPE(degradation products of decabromodiphenyl ethane)and MgF_(2),developing a fluorinated,flame-retardant separator with optimized ion channels,HDBDPE acts as both a low-toxicity flame retardant and an"F-element guide"through hydrogen bonding with MgF_(2),forming a uniform LiF SEI layer on the Li anode for rapid reaction kinetics.Moreover,under thermal runaway conditions,the MgF_(2)@HDBDPE/PP separator constructs a"high-efficiency flame-retardant barrier",effectively quenching free radicals and promoting the formation of MgBr_(2),thereby suppressing electrolyte combustion.As a result,both symmetric and full cells assembled with the MgF_(2)@HDBDPE/PP separator demonstrate superior cyclic stability and rate performance due to improved interfacial reactions.The MgF_(2)@HDBDPE/PP separator exhibits rapid flame retardancy under thermal runaway conditions.展开更多
To develop an efficient filter for removing white blood cells from whole blood,hydrophilic large-pore blended membranes of poly(vinylidene fluoride)(PVDF),polyvinyl pyrrolidone and polyethylene glycol,with good biocom...To develop an efficient filter for removing white blood cells from whole blood,hydrophilic large-pore blended membranes of poly(vinylidene fluoride)(PVDF),polyvinyl pyrrolidone and polyethylene glycol,with good biocompatibility,were prepared using the process of vapor-induced phase separation at various PVDF concentrations.The results demonstrated that at a PVDF mass concentration of 14%,the membrane had increased surface roughness,significantly enhanced hydrophilicity and wettability,and a wetting time of 8 s.The surface roughness of the membrane was also reduced to 31.637 nm.Furthermore,hemolysis rate and protein adsorption tests indicated that the blended membranes possessed excellent biocompatibility.They were reduced to 2.48%and 34.44μg·cm^(−2),respectively.The pore size of the fabricated membrane was relatively large,which reached approximately 8μm respectively,satisfying the filtration requirements.Lastly,the effects of different temperatures and multi-layered filters on leukocyte removal and the retention of red blood cells and platelets from whole blood were evaluated.The results revealed that the leukocyte removal rate was highest at 4℃ and with three membrane layers,the leukocyte removal rate was highest,reaching 98.36%,while the RBC and platelet content remained nearly unchanged compared with the original blood.This study provides a new approach for blood cell separation that is expected to play a significant role in medical fields such as blood transfusion demonstrating great potential for application and innovation.展开更多
The rapid decay of the surface wettability of plasma-treated polymers remains a critical limitation for their practical application in advanced materials.This study introduces a continuous atmospheric pressure plasma(...The rapid decay of the surface wettability of plasma-treated polymers remains a critical limitation for their practical application in advanced materials.This study introduces a continuous atmospheric pressure plasma(APP)technique for fabricating polyethylene(PE)separators with durable wettability,and elucidates the underlying mechanism.A systematic comparison of APP treatments with non-deposition and deposition gases,including Ar,Ar/O_(2),Ar/tetramethylcyclotetrasiloxane(TMCTS),and Ar/O_(2)/TMCTS,revealed the key impact factors in achieving durable wettability.Owing to the synergistic interactions of SiO_(x)C_(y)H_(z)nanoparticulate deposition,physical etching,and oxidative functionalization,the PE separator treated by Ar/O_(2)/TMCTS exhibited a 17.5-fold electrolyte wetting area compared to the original one.The improved surface energy and roughness of the SiO_(x)C_(y)H_(z)nanoparticle coating enhanced its electrochemical performance.The ionic conductivity increased by 1.9 times,while the charge transfer resistance decreased by 73.7%.Remarkably,owing to further oxidation of the SiO_(x)C_(y)H_(z)nanoparticle coating and the increase in its silica-like structure,the wetting area of the Ar/O_(2)/TMCTS-treated separator was still over 14-fold larger than that of the original separator after aging for 90 days.This study demonstrates an eco-friendly and scalable approach for fabricating high-performance battery separators and provides mechanistic insights into durable wettability by APP.展开更多
Lignocellulosic biomass is the most abundant re-newable resource on Earth,boasting advan-tages such as wide avail-ability and negative car-bon emissions.Especial-ly,efficient separation of lignocellulose into cellu-lo...Lignocellulosic biomass is the most abundant re-newable resource on Earth,boasting advan-tages such as wide avail-ability and negative car-bon emissions.Especial-ly,efficient separation of lignocellulose into cellu-lose,hemicellulose and lignin,and realizing val-orization of these compo-nents are more responsive to the development needs of biomass refinery and the green chem-istry era.This review outlines the main components of lignocellulose and briefly summerizes their utilization in chemical raw materials and energy production.It mainly focused on cur-rent advances in component separation methods of lignocellulose by organic solvents,ionic liquids and deep eutectic solvents.The design of separation methods,understanding of sepa-ration mechanisms,and optimization of reaction systems in each method are highlighted in detail.Furthermore,the ongoing challenges and future directions based on mechanism and in-dustrialization are critically discussed.Our goal is to elucidate the separation mechanisms and principles of method design,providing guidance for the development of highly efficient com-ponent separation methods of lignocellulose.展开更多
Methods of quantum information processing often appear in terms of specially selected states.For example,mutually unbiased bases(MUBs)and symmetric informationally complete measurements are widely applied.Finite frame...Methods of quantum information processing often appear in terms of specially selected states.For example,mutually unbiased bases(MUBs)and symmetric informationally complete measurements are widely applied.Finite frames have found use in many areas including quantum information.Due to its specific inner structure,a single equiangular tight frame(ETF)allows one to formulate criteria to detect non-classical correlations.This study aims to approach entanglement detection with the use of mutually unbiased ETFs.Such frames are an interesting generalization of widely recognized MUBs.It still uses rank-one operators,but the number of outcomes can exceed the dimensionality.Several approaches are considered including separability criteria and entanglement witnesses.Separability criteria for multipartite systems are finally obtained.展开更多
Zn-I_(2) batteries have emerged as promising next-generation energy storage systems owing to their inherent safety,environmental compatibility,rapid reaction kinetics,and small voltage hysteresis.Nevertheless,two crit...Zn-I_(2) batteries have emerged as promising next-generation energy storage systems owing to their inherent safety,environmental compatibility,rapid reaction kinetics,and small voltage hysteresis.Nevertheless,two critical challenges,i.e.,zinc dendrite growth and polyiodide shuttle effect,severely impede their commercial viability.To conquer these limitations,this study develops a multifunctional separator fabricated from straw-derived carboxylated nanocellulose,with its negative charge density further reinforced by anionic polyacrylamide incorporation.This modification simultaneously improves the separator’s mechanical properties,ionic conductivity,and Zn^(2+)ion transfer number.Remarkably,despite its ultrathin 20μm profile,the engineered separator demonstrates exceptional dendrite suppression and parasitic reaction inhibition,enabling Zn//Zn symmetric cells to achieve impressive cycle life(>1800 h at 2 m A cm^(-2)/2 m Ah cm^(-2))while maintaining robust performance even at ultrahigh areal capacities(25 m Ah cm^(-2)).Additionally,the separator’s anionic characteristic effectively blocks polyiodide migration through electrostatic repulsion,yielding Zn-I_(2) batteries with outstanding rate capability(120.7 m Ah g^(-1)at 5 A g^(-1))and excellent cyclability(94.2%capacity retention after 10,000 cycles).And superior cycling stability can still be achieved under zinc-deficient condition and pouch cell configuration.This work establishes a new paradigm for designing high-performance zinc-based energy storage systems through rational separator engineering.展开更多
Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional ...Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional groups of biochar exhibit varying degrees of influence on CO_(2)adsorption and separation performance under different adsorption conditions.Therefore,exploring the matching relationship between the physicochemical properties of biochar and its adsorption and separation performance at different adsorption conditions is essential for the development and optimization of carbon-based adsorbents.This study selected the high-performance extreme gradient boosting(XGB)algorithm from various algorithms and utilized it to develop CO_(2),N_(2),CH_(4)adsorption prediction models.Based on this,coupled prediction models were developed for CO_(2)/N_(2)and CO_(2)/CH_(4)adsorption selectivity.Furthermore,feature importance and partial dependence analysis were performed using SHAP values.The results indicate that during CO_(2)adsorption,the influence of the pore structure of biochar outweighs that of its chemical composition.Specifically,the pore structure of 0.4–0.6 nm is the most important property influencing CO_(2)adsorption at low and medium pressure(0–0.6 bar),and the pore structure of 0.6–0.8 nm,as well as the specific surface area contribute the most at high pressure(0.6–1 bar).During CO_(2)selective separation,the CO_(2)/N_(2)mixture is primarily separated through the selective adsorption of CO_(2)by nitrogen functional groups.In contrast,for CO_(2)/CH_(4)mixtures,pore structure<1 nm plays a more critical role in determining adsorption selectivity.In addition,molecular simulation studies further revealed the adsorption filling mechanisms of CO_(2)molecules within different pore sizes and functional groups.Finally,nitrogen-doped biochar was synthesized using de-alkalize lignin as the precursor,KOH as the activating agent,and urea as the nitrogen dopant.CO_(2),N_(2),and CH_(4)isothermal adsorption experiments were conducted,and the experimental results confirmed that the developed prediction models exhibit high accuracy(R^(2)>0.9).展开更多
Aqueous zinc-based batteries have emerged as promising candidates for large-scale energy storage owing to their inherent safety and cost-effectiveness.However,their widespread application is impeded by dendritic forma...Aqueous zinc-based batteries have emerged as promising candidates for large-scale energy storage owing to their inherent safety and cost-effectiveness.However,their widespread application is impeded by dendritic formation and parasitic reactions at zinc anodes.To address these issues,this study employs polyethyleneimine grafting and macropore filling to synergistically modify the cellulose separator.The zincophilic–NH_(2) and–NH–groups introduced by polyethyleneimine promote Zn^(2+)ion desolvation and nucleation processes.Concurrently,the nanocellulose incorporated into macropores not only significantly enhances mechanical properties but also compensates for macroporous defects within the cellulose separator.The optimized separator exhibits ultralow thickness(18μm),ultrahigh modulus(3.2 GPa),large ionic conductivity(19.0 mS cm^(-1)),high Zn^(2+)ion transfer number(0.63),and good biodegradability.Comprehensive experimental measurements and theoretical analysis reveal that the utilization of this separator contributes to significantly suppressed zinc dendrites and improved electrochemical kinetics.The assembled Zn//Zn cell demonstrates exceptional cycling stability(over 1000 h lifespan at10 m A cm^(-2)and 2 mAh cm^(-2)),and the Zn//MnO_(2) and Zn//I_(2) full batteries maintain excellent longterm cyclability under high cathode mass loadings.This work advances our understanding of multifunctional separator design for next-generation electrochemical energy storage systems.展开更多
The structural design and performance characteristics of the diaphragm have a decisive impact on the safety and electrochemical performance of lithium-ion batteries(LIBs).However,traditional polyolefin diaphragms stil...The structural design and performance characteristics of the diaphragm have a decisive impact on the safety and electrochemical performance of lithium-ion batteries(LIBs).However,traditional polyolefin diaphragms still face challenges in simultaneously improving the ion transport efficiency and thermal stability.Here,we report an in situ dynamic lithium compensation strategy for manufacturing a biobased furan aramid/ceramic diaphragm(BAS)with higher thermal stability and ion transport efficiency.Specifically,exchangeable carboxyl groups(–COOH)are introduced into the bio-based furan aramid(BA)framework,which are in situ converted into–COOLi groups to form lithium ions(Li^(+))transport channels,achieving dynamic compensation of active Li^(+).The dual transmission system of ion exchange and physical pore channels synergistically enhances the ionic conductivity of BAS to 1.536 mS cm^(-1).The high polarity structure of the furan ring and the electrolyte have excellent compatibility,significantly reducing the solid–liquid interfacial energy,making BAS have extremely high electrolyte wettability(contact angle of 0°).The BA amide group forms a multi-scale bonding network with the nano-ceramics.The BAS prepared by the water-coating process exhibits excellent thermal stability(with a thermal shrinkage rate of less than 1%after 1 h at 150℃).The LiFePO_(4)|Li half-cell assembled with BAS shows a capacity retention rate of up to 91.7%after 280 cycles at 1C,with a Coulomb efficiency of 99%,demonstrating excellent cycling stability.This design and development based on bio-materials provides a new approach for high safety and high energy density battery systems.展开更多
Traditional nanofiltration membranes face challenges such as membrane fouling and difficulties in achieving precise separation of small organic molecules.A promising solution to these issues is the preparation of thin...Traditional nanofiltration membranes face challenges such as membrane fouling and difficulties in achieving precise separation of small organic molecules.A promising solution to these issues is the preparation of thin-film nanocomposite membranes.In this study,Cu and Ag bimetals were incorporated into covalent organic frameworks to fabricate thin-film nanocomposite membranes.The hydrophilic monomer 1,3,5-tris(4-aminophenyl)benzene of covalent organic frameworks was introduced as a water phase monomer during interfacial polymerization to enhance the organic-inorganic compatibility.The incorporated covalent organic frameworks within the thin-film nanocomposite membrane loosened the selective layer,resulting in an enhanced permeability of 24.6 LMH bar^(-1).The membrane exhibited a rejection rate over 99.0%for Congo Red,Xylene Brilliant Cyanine G,and Reactive Blue,while exhibiting relatively low rejection rates of MgCl_(2) and NaCl.Moreover,the outstanding catalytic capability of the incorporated bimetals led to a 4-nitrophenol conversion rate of 84.38%,enabling simultaneous conversion and separation.The integration of covalent organic frameworks and bimetals also imparted robust antibacterial properties,significantly enhancing operational stability.In conclusion,the covalent organic framework-Cu/Ag-based thin-film nanocomposite membrane demonstrated superior catalytic and separation capabilities,presenting a promising alternative for advanced filtration applications.展开更多
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.
文摘The existence of absorption and reflection of light underwater leads to problems such as color distortion and blue-green bias in underwater images.In this study,a depthwise separable convolution-based generative adversarial network(GAN)algorithm was proposed.Taking GAN as the basic framework,it combined a depthwise separable convolution module,attention mechanism,and reconstructed convolution module to realize the enhancement of underwater degraded images.Multi-scale features were captured by the depthwise separable convolution module,and the attention mechanism was utilized to enhance attention to important features.The reconstructed convolution module further extracts and fuses local and global features.Experimental results showed that the algorithm performs well in improving the color bias and blurring of underwater images,with PSNR reaching 27.835,SSIM reaching 0.883,UIQM reaching 3.205,and UCIQE reaching 0.713.The enhanced image outperforms the comparison algorithm in both subjective and objective metrics.
基金supported by Shaanxi Key Research and Development Program(No.2024SF-YBXM-546)the National Natural Science Foundation of China(No.52470161)the State Key Laboratory of Pollution Control and Resource Reuse Foundation(No.PCRRF21007).
文摘With the legislative development,the organic and inorganic composition separation has become the primary requirement for sewer sediment disposal,however the relevant technology has been rarely reported and the driving mechanism was still unclear.In this study,direct disintegration of biopolymers and indirect broken of connection point were investigated on the hydrolysis and component separation.Three typical sewer sediment treatment approaches,i.e.,alkaline,thermal and cation exchange treatments were proposed,which represented the hydrolysis-driving forces of chemical hydrolysis,physical hydrolysis and innovative cation bridging break-age.The results showed that the organic and inorganic separation rates of sewer sediment driven by alkaline,thermal and cation exchange treatments reached 21.26%,23.80%,and 19.56%-48.0%,respectively,compared to 4.43%in control.The secondary structure of proteins was disrupted,transitioning from𝛼α-helix to𝛽β-turn and random coil.Meanwhile,much biopolymers were released from solid to the liquid phase.From thermody-namic perspective,sewer sediment deposition was controlled by short-range interfacial interactions described by extended Derjaguin-Landau-Verwey-Overbeek theory.Additionally,the separation of organic and inorganic components was positively correlated with the thermodynamic parameters(Corr=0.87),highlighted the robust-ness of various driving forces.And the flocculation energy barriers were 2.40(alkaline),1.60 times(thermal),and 4.02–4.97 times(cation exchange)compared to control group.The findings revealed the contrition differ-ence of direct disintegration of gelatinous biopolymers and indirect breakage of composition connection sites in sediment composition separation,filling the critical gaps in understanding the specific mechanisms of sediment biopolymer disintegration and intermolecular connection breakage.
基金the financial support from the National Natural Science Foundation of China(22408182)the Young Talents of Science and Technology in Universities of Inner Mongolia Autonomous Region(NJYT24024)the Natural Science Foundation of Inner Mongolia Autonomous Region(2023QN02007 and 2025QN02009)。
文摘Lithium(Li)dendrites,resulting from poor ion desolvation and transport behavior at the anode/electrolyte interface during electrodeposition,severely impede the practicality of Li metal anodes.Inspired by the transmembrane cascade transport mechanism of biological ion pumps,we design a biomimetic dual-cascade separator(BDS)based on gradient pore core–shell Gd_(2)O_(3)@ZIF-7 nanoparticles to stabilize Li metal anodes.The mesoporous Gd_(2)O_(3)core,via Lewis acidic surface,weakens Li^(+) -solvent interactions,thereby reconstructing the solvation structure and achieving pre-desolvation.The microporous ZIF-7 shell then promotes final desolvation through strong confinement effect and N-rich site coordination,while its nanochannels homogenize Li^(+) transport.This synergistic meso/microporous gradient creates a unique dual-cascade effect for ion desolvation and transport.Consequently,BDS achieves a low desolvation energy barrier,a high Li^(+) transference number(0.71),and dendrite-free Li deposition.The average Coulombic efficiency rises from 72.7%to 98.4%,the cycling performance of the Li||Li symmetrical cell improves by 3.2 times,and the capacity retention of LiFePO_4(LFP)||Li full cell increases from 38.3%to73.4%after 500 cycles.This work offers a novel separator design concept,deepens Li deposition understanding,and guides separators from passive protection to active regulation.
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Project supported by the National Key Research and Development Program of China(2022YFC2905800)National Natural Science Foundation of China(52374276,52274269)+2 种基金Yunnan Fundamental Re search Projects(202401AS070051)the Natural Science Foundation of Hubei Province of China(2024AFD123)Young Elite Scientists Sponsorship Program by CAST(YESS20200276)。
文摘The efficient flotation separation of rare earth elements(REEs)from gangue minerals is crucial in mineral processing.This study synthesized a quaternary ammonium salt ionic liquid collector,tetrabutylammonium salicylhydroxamate(T-S),and investigated its performance in separating bastnaesite and fluorite.T-S was synthesized from salicylhydroxamic acid(SHA)and tetrabutylammonium chloride(TBAC),and its molecular structure was characterized using Fourier transform infrared(FTIR)spectroscopy.Microflotation tests indicate that T-S outperforms SHA and TBAC in both collecting ability and selectivity for bastnaesite.Adsorption,zeta potential,and infrared spectroscopy measurements reveal that T-S exhibits stronger adsorption on bastnaesite compared to SHA and TBAC.X-ray photoelectron spectroscopy(XPS)and molecular dynamics simulations(MDS)results confirm that chemical adsorption occurs between Ce on the bastnaesite surface and the-C(=O)NHOH groups of T-S.Moreover,the interaction between T-S and the bastnaesite surface is stronger than that with the fluorite surface.This work provides valuable insights for designing ionic liquid collectors for the flotation separation of bastnaesite and fluorite.
基金Project supported by the National Key R&D Program of China(2022YFC2905800)the National Natural Science Foundation of China(52174242)the National Youth Talent Support Program(QNBJ-2023-03)。
文摘Bayan Obo rare earth mine is the largest light rare earth resource worldwide,primarily extracts rare earth elements(REEs)from mixed RE concentrates with bastnaesite and monazite.Nevertheless,the adoption of the concentrated sulfuric acid roasting metallurgical process has resulted in damage to the environment.Therefore,this paper adopted the method of selective mineral phase transformation(MPT)followed by enhanced micro-flotation.By determining the optimal MPT co nditions,the flotation recovery of bastnaesite-roasted products by the collector(phthalic acid,PA)is improved,and the enhanced separation of bastnaesite with monazite is realized.The results show that with the increase of roasting temperature and time,the bastnaesite decomposition product is CeOF and monazite does not change significantly.Subsequent micro-flotation exhibits a gradual decline in the PA consumption of bastnaesiteroasted products,while the flotation recovery of monazite-roasted products remains poor.The artificial mixed ore experiments result in a CeOF foam product with a content of 94.14%and a recovery of 85.80%,and a monazite tank product with a content of 73.53%and a recovery of 87.87%.Compared with the preroasting ore,the surface and interior of bastnaesite-roasted products develop numerous cracks and porosities,and no obvious structural damage is observed in monazite-roasted particles.As the roasting temperature increases,the mineral particles undergo recrystallization or closure,reducing the specific surface area of bastnaesite-roasted products and enhancing hydrophobicity,leading to diminished PA consumption.Fourier transform infrared and other flotation-relation tests show that PA is chemisorbed on the surface of CeOF.The MPT conditions are optimized in this study,which provides a reference for further advancing the efficient separation of bastnaesite and monazite.
基金supported by the National Natural Science Foundation of China (52172228)the Natural Science Foundation of Fujian Province (2024J01475 and 2023J05127)
文摘Lithium-sulfur batteries(LSBs)represent a next-generation energy storage technology,but widespread applications are restricted by the shuttle of lithium polysulfides(LiPSs).The rational design of separators has been demonstrated to be one of the most efficient and cost-effective strategies to curb the shuttle effect,and tremendous research progress has been achieved.The efficiency of a separator depends on its interaction with LiPSs,which is governed by the surface energy and binding strength.Despite several review works that have been reported to advance the separators,most of them primarily focus on active material innovation and construction.The most crucial issues of surface binding energy have not been systematically reviewed,limiting the precise design of efficient separators.In this review,fundamentals related to surface energy and binding interactions with LiPSs are comprehensively analyzed and discussed.With surface binding and energy main lines,the advancements in separator engineering strategies are elaborately summarized and discussed.Moreover,techniques for evaluating affinity to LiPSs are thoroughly analyzed to avoid any ambiguities in measurement.Based on the research context,valuable research directions are suggested to construct efficient separators.This work provides guidelines to regulate the surface binding and energy of separators for high-performance LSBs.
基金supported by the National Natural Science Foundation of China(No.22375063)Science and Technology Commission of Shanghai Municipality(No.23JC1401700)the Fundamental Research Funds for the Central Universities.
文摘Developing advanced polymeric materials with enhanced mechanical properties and functionalities has been a long-standing goal in materials science.Recently,supramolecular polymeric materials (SPMs) have drawn increased attention due to their unique properties and potential applications in self-healing,shape memory,sensors,and flexible electronics.Here,we develop an ionic cluster-optimized microphase separation strategy to enhance the toughening and energy dissipation capabilities of polydisulfide-based supramolecular polymers.The mechanical properties,including Young’s modulus and toughness,are significantly improved by integrating the quadruple H-bonding 2-ureido-4-pyrimidone (UPy) induced microphase separation with iron(Ⅲ)-to-carboxylate ionic clusters.By combining established chemical approaches with adjustable polymer phase ratios,it is revealed that the synergistic effect of these factors expands the interchain spacing,facilitates the formation of microphase domains,and enhances the tolerance of polythioctic acid-based polymers to external mechanical and thermal stimuli,meeting the practical requirements for industrial plastic applications.Moreover,the UPy-functionalized polymers incorporating iron carboxylate clusters exhibit good one-way shape memory behavior with practical applicability at a relatively low recovery temperature.Our work demonstrates a novel strategy for constructing industrially viable shape memory dynamic SPMs and paves the way for future innovations in developing SPMs.
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(52401283)National Natural Science Foundation of Jiangsu Province(BK20230933)+1 种基金Fundamental Research Funds for the Central Universities(No.30925010524)Young Faculty Development Fund of Nanjing University of Science and Technology。
文摘Traditional fluorination strategies have attracted significant attention due to their ability to construct a fluorine-rich solid-electrolyte interphase(SEI)at the anode-electrolyte interface.However,the inhomogeneous distribution of LiF within the SEI layer remains a critical challenge that hinders the effective suppression of lithium dendrite growth.This work explores the synergy between HDBDPE(degradation products of decabromodiphenyl ethane)and MgF_(2),developing a fluorinated,flame-retardant separator with optimized ion channels,HDBDPE acts as both a low-toxicity flame retardant and an"F-element guide"through hydrogen bonding with MgF_(2),forming a uniform LiF SEI layer on the Li anode for rapid reaction kinetics.Moreover,under thermal runaway conditions,the MgF_(2)@HDBDPE/PP separator constructs a"high-efficiency flame-retardant barrier",effectively quenching free radicals and promoting the formation of MgBr_(2),thereby suppressing electrolyte combustion.As a result,both symmetric and full cells assembled with the MgF_(2)@HDBDPE/PP separator demonstrate superior cyclic stability and rate performance due to improved interfacial reactions.The MgF_(2)@HDBDPE/PP separator exhibits rapid flame retardancy under thermal runaway conditions.
基金The National Key Research and Development Program of China(2020YFC0862903)Supported by Jiangsu Future Membrane Technology Innovation Center(BM2021804)National Foreign Expert Program(H20240294).
文摘To develop an efficient filter for removing white blood cells from whole blood,hydrophilic large-pore blended membranes of poly(vinylidene fluoride)(PVDF),polyvinyl pyrrolidone and polyethylene glycol,with good biocompatibility,were prepared using the process of vapor-induced phase separation at various PVDF concentrations.The results demonstrated that at a PVDF mass concentration of 14%,the membrane had increased surface roughness,significantly enhanced hydrophilicity and wettability,and a wetting time of 8 s.The surface roughness of the membrane was also reduced to 31.637 nm.Furthermore,hemolysis rate and protein adsorption tests indicated that the blended membranes possessed excellent biocompatibility.They were reduced to 2.48%and 34.44μg·cm^(−2),respectively.The pore size of the fabricated membrane was relatively large,which reached approximately 8μm respectively,satisfying the filtration requirements.Lastly,the effects of different temperatures and multi-layered filters on leukocyte removal and the retention of red blood cells and platelets from whole blood were evaluated.The results revealed that the leukocyte removal rate was highest at 4℃ and with three membrane layers,the leukocyte removal rate was highest,reaching 98.36%,while the RBC and platelet content remained nearly unchanged compared with the original blood.This study provides a new approach for blood cell separation that is expected to play a significant role in medical fields such as blood transfusion demonstrating great potential for application and innovation.
基金supported by the National Natural Science Foundation of China(No.12075054)the Fundamental Research Funds for the Central Universities(No.CUSF-DH-T-2024069)。
文摘The rapid decay of the surface wettability of plasma-treated polymers remains a critical limitation for their practical application in advanced materials.This study introduces a continuous atmospheric pressure plasma(APP)technique for fabricating polyethylene(PE)separators with durable wettability,and elucidates the underlying mechanism.A systematic comparison of APP treatments with non-deposition and deposition gases,including Ar,Ar/O_(2),Ar/tetramethylcyclotetrasiloxane(TMCTS),and Ar/O_(2)/TMCTS,revealed the key impact factors in achieving durable wettability.Owing to the synergistic interactions of SiO_(x)C_(y)H_(z)nanoparticulate deposition,physical etching,and oxidative functionalization,the PE separator treated by Ar/O_(2)/TMCTS exhibited a 17.5-fold electrolyte wetting area compared to the original one.The improved surface energy and roughness of the SiO_(x)C_(y)H_(z)nanoparticle coating enhanced its electrochemical performance.The ionic conductivity increased by 1.9 times,while the charge transfer resistance decreased by 73.7%.Remarkably,owing to further oxidation of the SiO_(x)C_(y)H_(z)nanoparticle coating and the increase in its silica-like structure,the wetting area of the Ar/O_(2)/TMCTS-treated separator was still over 14-fold larger than that of the original separator after aging for 90 days.This study demonstrates an eco-friendly and scalable approach for fabricating high-performance battery separators and provides mechanistic insights into durable wettability by APP.
基金supported by National Key Technolo-gy R&D Program of China(2023YFD1701505)De-velopment Projects in Anhui Province(2022107020013).
文摘Lignocellulosic biomass is the most abundant re-newable resource on Earth,boasting advan-tages such as wide avail-ability and negative car-bon emissions.Especial-ly,efficient separation of lignocellulose into cellu-lose,hemicellulose and lignin,and realizing val-orization of these compo-nents are more responsive to the development needs of biomass refinery and the green chem-istry era.This review outlines the main components of lignocellulose and briefly summerizes their utilization in chemical raw materials and energy production.It mainly focused on cur-rent advances in component separation methods of lignocellulose by organic solvents,ionic liquids and deep eutectic solvents.The design of separation methods,understanding of sepa-ration mechanisms,and optimization of reaction systems in each method are highlighted in detail.Furthermore,the ongoing challenges and future directions based on mechanism and in-dustrialization are critically discussed.Our goal is to elucidate the separation mechanisms and principles of method design,providing guidance for the development of highly efficient com-ponent separation methods of lignocellulose.
文摘Methods of quantum information processing often appear in terms of specially selected states.For example,mutually unbiased bases(MUBs)and symmetric informationally complete measurements are widely applied.Finite frames have found use in many areas including quantum information.Due to its specific inner structure,a single equiangular tight frame(ETF)allows one to formulate criteria to detect non-classical correlations.This study aims to approach entanglement detection with the use of mutually unbiased ETFs.Such frames are an interesting generalization of widely recognized MUBs.It still uses rank-one operators,but the number of outcomes can exceed the dimensionality.Several approaches are considered including separability criteria and entanglement witnesses.Separability criteria for multipartite systems are finally obtained.
基金the financial support from the Natural Science Foundation of Jiangsu Province(BK20231292)the Jiangsu Agricultural Science and Technology Innovation Fund(CX(24)3091)+6 种基金the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX25_1429)the National Key R&D Program of China(2024YFE0109200)the Fundamental Research Funds for the Central Universities(No.2024300440)Guangdong Basic and Applied Basic Research Foundation(2025A1515011098)the National Natural Science Foundation of China(12464032)the Natural Science Foundation of Jiangxi Province(20232BAB201032)Ji'an Science and Technology Plan Project(2024H-100301)。
文摘Zn-I_(2) batteries have emerged as promising next-generation energy storage systems owing to their inherent safety,environmental compatibility,rapid reaction kinetics,and small voltage hysteresis.Nevertheless,two critical challenges,i.e.,zinc dendrite growth and polyiodide shuttle effect,severely impede their commercial viability.To conquer these limitations,this study develops a multifunctional separator fabricated from straw-derived carboxylated nanocellulose,with its negative charge density further reinforced by anionic polyacrylamide incorporation.This modification simultaneously improves the separator’s mechanical properties,ionic conductivity,and Zn^(2+)ion transfer number.Remarkably,despite its ultrathin 20μm profile,the engineered separator demonstrates exceptional dendrite suppression and parasitic reaction inhibition,enabling Zn//Zn symmetric cells to achieve impressive cycle life(>1800 h at 2 m A cm^(-2)/2 m Ah cm^(-2))while maintaining robust performance even at ultrahigh areal capacities(25 m Ah cm^(-2)).Additionally,the separator’s anionic characteristic effectively blocks polyiodide migration through electrostatic repulsion,yielding Zn-I_(2) batteries with outstanding rate capability(120.7 m Ah g^(-1)at 5 A g^(-1))and excellent cyclability(94.2%capacity retention after 10,000 cycles).And superior cycling stability can still be achieved under zinc-deficient condition and pouch cell configuration.This work establishes a new paradigm for designing high-performance zinc-based energy storage systems through rational separator engineering.
基金supported by the Fundamental Research Funds for the Central Universities(No.2025JC008)the National Natural Science Foundation of China(grant number 52176105)+2 种基金the Science and Technology Project of Hebei Education Department-China(BJK2022063)the Hebei Natural Science Foundation-China(grant number E2025502038)the Funding Program for Cultivating Innovative Abilities of Graduate Students in Hebei Province of China(CXZZBS2025184).
文摘Biochar has been widely recognized as a promising solid CO_(2)adsorbent with economic and ecological benefits.Industrial CO_(2)emissions originate from diverse sources,while the pore structure and chemical functional groups of biochar exhibit varying degrees of influence on CO_(2)adsorption and separation performance under different adsorption conditions.Therefore,exploring the matching relationship between the physicochemical properties of biochar and its adsorption and separation performance at different adsorption conditions is essential for the development and optimization of carbon-based adsorbents.This study selected the high-performance extreme gradient boosting(XGB)algorithm from various algorithms and utilized it to develop CO_(2),N_(2),CH_(4)adsorption prediction models.Based on this,coupled prediction models were developed for CO_(2)/N_(2)and CO_(2)/CH_(4)adsorption selectivity.Furthermore,feature importance and partial dependence analysis were performed using SHAP values.The results indicate that during CO_(2)adsorption,the influence of the pore structure of biochar outweighs that of its chemical composition.Specifically,the pore structure of 0.4–0.6 nm is the most important property influencing CO_(2)adsorption at low and medium pressure(0–0.6 bar),and the pore structure of 0.6–0.8 nm,as well as the specific surface area contribute the most at high pressure(0.6–1 bar).During CO_(2)selective separation,the CO_(2)/N_(2)mixture is primarily separated through the selective adsorption of CO_(2)by nitrogen functional groups.In contrast,for CO_(2)/CH_(4)mixtures,pore structure<1 nm plays a more critical role in determining adsorption selectivity.In addition,molecular simulation studies further revealed the adsorption filling mechanisms of CO_(2)molecules within different pore sizes and functional groups.Finally,nitrogen-doped biochar was synthesized using de-alkalize lignin as the precursor,KOH as the activating agent,and urea as the nitrogen dopant.CO_(2),N_(2),and CH_(4)isothermal adsorption experiments were conducted,and the experimental results confirmed that the developed prediction models exhibit high accuracy(R^(2)>0.9).
基金the financial support from the Natural Science Foundation of Jiangsu Province(BK20231292)the Jiangsu Agricultural Science and Technology Innovation Fund(CX(24)3091)+7 种基金the National Key R&D Program of China(2024YFE0109200)the Fundamental Research Funds for the Central Universities(No.2024300440)the Guangdong Basic and Applied Basic Research Foundation(2025A1515011098)the Postgraduate Research&Practice Innovation Program of Jiangsu Province(KYCX24_1299)the National Natural Science Foundation of China(12464032)the Natural Science Foundation of Jiangxi Province(20232BAB201032)the Ji’an Science and Technology Plan Project(2024H-100301)supported by the high-performance computing campus level public platform of Jinggangshan University。
文摘Aqueous zinc-based batteries have emerged as promising candidates for large-scale energy storage owing to their inherent safety and cost-effectiveness.However,their widespread application is impeded by dendritic formation and parasitic reactions at zinc anodes.To address these issues,this study employs polyethyleneimine grafting and macropore filling to synergistically modify the cellulose separator.The zincophilic–NH_(2) and–NH–groups introduced by polyethyleneimine promote Zn^(2+)ion desolvation and nucleation processes.Concurrently,the nanocellulose incorporated into macropores not only significantly enhances mechanical properties but also compensates for macroporous defects within the cellulose separator.The optimized separator exhibits ultralow thickness(18μm),ultrahigh modulus(3.2 GPa),large ionic conductivity(19.0 mS cm^(-1)),high Zn^(2+)ion transfer number(0.63),and good biodegradability.Comprehensive experimental measurements and theoretical analysis reveal that the utilization of this separator contributes to significantly suppressed zinc dendrites and improved electrochemical kinetics.The assembled Zn//Zn cell demonstrates exceptional cycling stability(over 1000 h lifespan at10 m A cm^(-2)and 2 mAh cm^(-2)),and the Zn//MnO_(2) and Zn//I_(2) full batteries maintain excellent longterm cyclability under high cathode mass loadings.This work advances our understanding of multifunctional separator design for next-generation electrochemical energy storage systems.
基金the financial support from the National Natural Science Foundation of China(22293011,T2341001)the Major Science and Technology Project of Anhui Province(202203a06020010)+1 种基金the Horizontal Project Provided by Jiangsu Zhuogao New Materials Technology Co.,Ltd.(Td00923003H)Joint Laboratory by China Power Investment Ronghe New Energy Technology Co.,Ltd.and the Central Government Guiding Special Fund Project for Local Science and Technology Development(202407a12020008)。
文摘The structural design and performance characteristics of the diaphragm have a decisive impact on the safety and electrochemical performance of lithium-ion batteries(LIBs).However,traditional polyolefin diaphragms still face challenges in simultaneously improving the ion transport efficiency and thermal stability.Here,we report an in situ dynamic lithium compensation strategy for manufacturing a biobased furan aramid/ceramic diaphragm(BAS)with higher thermal stability and ion transport efficiency.Specifically,exchangeable carboxyl groups(–COOH)are introduced into the bio-based furan aramid(BA)framework,which are in situ converted into–COOLi groups to form lithium ions(Li^(+))transport channels,achieving dynamic compensation of active Li^(+).The dual transmission system of ion exchange and physical pore channels synergistically enhances the ionic conductivity of BAS to 1.536 mS cm^(-1).The high polarity structure of the furan ring and the electrolyte have excellent compatibility,significantly reducing the solid–liquid interfacial energy,making BAS have extremely high electrolyte wettability(contact angle of 0°).The BA amide group forms a multi-scale bonding network with the nano-ceramics.The BAS prepared by the water-coating process exhibits excellent thermal stability(with a thermal shrinkage rate of less than 1%after 1 h at 150℃).The LiFePO_(4)|Li half-cell assembled with BAS shows a capacity retention rate of up to 91.7%after 280 cycles at 1C,with a Coulomb efficiency of 99%,demonstrating excellent cycling stability.This design and development based on bio-materials provides a new approach for high safety and high energy density battery systems.
基金sponsored by the National Natural Science Foundation of China(Grant No.NSFC-22378160 and U23A20688).
文摘Traditional nanofiltration membranes face challenges such as membrane fouling and difficulties in achieving precise separation of small organic molecules.A promising solution to these issues is the preparation of thin-film nanocomposite membranes.In this study,Cu and Ag bimetals were incorporated into covalent organic frameworks to fabricate thin-film nanocomposite membranes.The hydrophilic monomer 1,3,5-tris(4-aminophenyl)benzene of covalent organic frameworks was introduced as a water phase monomer during interfacial polymerization to enhance the organic-inorganic compatibility.The incorporated covalent organic frameworks within the thin-film nanocomposite membrane loosened the selective layer,resulting in an enhanced permeability of 24.6 LMH bar^(-1).The membrane exhibited a rejection rate over 99.0%for Congo Red,Xylene Brilliant Cyanine G,and Reactive Blue,while exhibiting relatively low rejection rates of MgCl_(2) and NaCl.Moreover,the outstanding catalytic capability of the incorporated bimetals led to a 4-nitrophenol conversion rate of 84.38%,enabling simultaneous conversion and separation.The integration of covalent organic frameworks and bimetals also imparted robust antibacterial properties,significantly enhancing operational stability.In conclusion,the covalent organic framework-Cu/Ag-based thin-film nanocomposite membrane demonstrated superior catalytic and separation capabilities,presenting a promising alternative for advanced filtration applications.
