Inherent complexity of plant metabolites necessitates the use of multi-dimensional information to accomplish comprehensive profiling and confirmative identification.A dimension-enhanced strategy,by offline two-dimensi...Inherent complexity of plant metabolites necessitates the use of multi-dimensional information to accomplish comprehensive profiling and confirmative identification.A dimension-enhanced strategy,by offline two-dimensional liquid chromatography/ion mobility-quadrupole time-of-flight mass spectrometry(2 D-LC/IM-QTOF-MS)enabling four-dimensional separations(2 D-LC,IM,and MS),is proposed.In combination with in-house database-driven automated peak annotation,this strategy was utilized to characterize ginsenosides simultaneously from white ginseng(WG)and red ginseng(RG).An offline 2 DLC system configuring an Xbridge Amide column and an HSS T3 column showed orthogonality 0.76 in the resolution of ginsenosides.Ginsenoside analysis was performed by data-independent high-definition MSE(HDMSE)in the negative ESI mode on a Vion?IMS-QTOF hybrid high-resolution mass spectrometer,which could better resolve ginsenosides than MSEand directly give the CCS information.An in-house ginsenoside database recording 504 known ginsenosides and 58 reference compounds,was established to assist the identification of ginsenosides.Streamlined workflows,by applying UNIFI?to automatedly annotate the HDMSEdata,were proposed.We could separate and characterize 323 ginsenosides(including 286 from WG and 306 from RG),and 125 thereof may have not been isolated from the Panax genus.The established 2 D-LC/IM-QTOF-HDMSEapproach could also act as a magnifier to probe differentiated components between WG and RG.Compared with conventional approaches,this dimensionenhanced strategy could better resolve coeluting herbal components and more efficiently,more reliably identify the multicomponents,which,we believe,offers more possibilities for the systematic exposure and confirmative identification of plant metabolites.展开更多
Developing a new strategy for the synthesis of high-nuclear transition metal(TM)cluster substituted polyoxometalates(POMs)provides an avenue for new materials with unique functions.Herein,the synergetic coordination s...Developing a new strategy for the synthesis of high-nuclear transition metal(TM)cluster substituted polyoxometalates(POMs)provides an avenue for new materials with unique functions.Herein,the synergetic coordination strategy of 1,2,4-1H-triazole(Htrz),ethylenediamine(en),and a lacunary POM was applied to construct a highnuclear Ni cluster substituted POM.As a result,a{Ni_(30)}cluster substituted POM,[Ni(trz)3]2@[Ni_(30)(H2O)16]POM.展开更多
Aggregation-induced emission(AIE)polymers have been extensively studied;however,the integration of AIE units into polyelectrolytes remains largely limited by the laborious multistep synthesis of pre-designed emissive ...Aggregation-induced emission(AIE)polymers have been extensively studied;however,the integration of AIE units into polyelectrolytes remains largely limited by the laborious multistep synthesis of pre-designed emissive monomers.Herein,we report a one-pot multicomponent polymerization method that directly produces main-chain charged polyelectrolytes with intrinsic AIE characteristics from non-emissive building blocks.By optimizing the monomer structures and reaction conditions,a series of soluble high-molecular-weight polymers with welldefined backbones were obtained in high yields.The resulting polyelectrolytes displayed robust AIE behavior,exhibiting fluorescence enhancement up to about 60-fold in an aqueous environment,and maintained excellent thermal stability.Owing to their cationic backbones,these polymers interact strongly with microbial surfaces and exhibit remarkable antimicrobial activities.This study establishes a synthetically efficient route to AIE polyelectrolytes and highlights their potential applications as multifunctional materials for bioimaging,antimicrobial therapy,and other applications.展开更多
This study investigates the microstructure and co-precipitation behavior of multicomponent(Ni(Al,Mn)and Cu)nanoparticles in the weld heat-affected zones of high-strength low-carbon steel.Through thermal simulations,th...This study investigates the microstructure and co-precipitation behavior of multicomponent(Ni(Al,Mn)and Cu)nanoparticles in the weld heat-affected zones of high-strength low-carbon steel.Through thermal simulations,the intercritical,fine-grained,and coarsegrained heat-affected zones were systematically characterized to elucidate the interplay between the microstructure,precipitation,and mechanical properties.At a heat input of 30 kJ·cm^(−1),Ni(Al,Mn)nanoparticles dissolve in the intercritical heat-affected zone,followed by dense reprecipitation coupled with significant coarsening of Cu particles during cooling,thereby retaining high strength but reducing impact toughness to(142±10)J(compared to(205±8)J of the base metal).The fine-grained heat-affected zone,under the same heat input,exhibits a refined ferritic-bainite matrix with a few fine Ni(Al,Mn)and slightly coarsened Cu particles,thus enhancing plastic deformation capacity and resulting in superior impact toughness of(196±7)J.Despite complete dissolution of original precipitates at peak temperatures in the coarse-grained heat-affected zone,re-precipitated nanoparticles provide effective strengthening effect,compensating for grain coarsening and dislocation recovery and resulting in an impressive impact toughness of(186±6)J.The toughening mechanism is primarily attributed to the synergistic actions of the matrix,precipitates,and deformation twins.These findings provide mechanistic and quantitative insights for developing processing-microstructure-property relationships in different welding heat-affected zones,and this framework can be further utilized to optimize welding parameters for tailored applications.展开更多
The complex interactions and conflicting performance demands in multi-component composites pose significant challenges for achieving balanced multi-property optimization through conventional trial-and-error approaches...The complex interactions and conflicting performance demands in multi-component composites pose significant challenges for achieving balanced multi-property optimization through conventional trial-and-error approaches.Machine learning(ML)offers a promising solution,markedly improving materials discovery efficiency.However,the high dimensionality of feature spaces in such systems has long impeded effective ML-driven feature representation and inverse design.To overcome this,we present an Intelligent Screening System(ISS)framework to accelerate the discovery of optimal formulations balancing four key properties in 15-component PTFE-based copper-clad laminate composites(PTFE-CCLCs).ISS adopts modular descriptors based on the physical information of component volume fractions,thereby simplifying the feature representation.By leveraging the inverse prediction capability of ML models and constructing a performance-driven virtual candidate database,ISS significantly reduced the computational complexity associated with high-dimensional spaces.Experimental validation confirmed that ISSoptimized formulations exhibited superior synergy,notably resolving the trade-off between thermal conductivity and peel strength,and outperform many commercial counterparts.Despite limited data and inherent process variability,ISS achieved an average prediction accuracy of 76.5%,with thermal conductivity predictions exceeding 90%,demonstrating robust reliability.This work provides an innovative,efficient strategy for multifunctional optimization and accelerated discovery in ultra-complex composite systems,highlighting the integration of ML and advanced materials design.展开更多
The development of a new precipitation-strengthened Ni-based superalloy relies on a seemingly contradictory yet crucial trade-off between‘easy-to-deform’and‘high strength’.Commercial Haynes 282(Ni-20Cr-10Co-8.5Mo-...The development of a new precipitation-strengthened Ni-based superalloy relies on a seemingly contradictory yet crucial trade-off between‘easy-to-deform’and‘high strength’.Commercial Haynes 282(Ni-20Cr-10Co-8.5Mo-2.1Ti-1.5Al)has a good balance of mechanical properties and formability,but it still faces growing concerns regarding material cost and applicability due to the high concentration of Co(∼10 wt%).Therefore,it is necessary to develop Co-free,easy-to-deform and low-cost alloys with thermomechanical processing capabilities and mechanical properties comparable to those of Haynes 282.Both Ni and Fe are selected to replace Co,because the atomic sizes of Fe,Ni and Co are almost identical(∼0.125 nm).Moreover,the moduli of Co and Fe are all 82 GPa,which is only 7%higher than that of Ni(76 GPa).The effects of Co substitution by Ni/Fe on the alloy microstructures and mechanical properties are investigated.Substitution of Co with Ni/Fe does not change the size and volume fraction of theγ′phase,nor does it change the partitioning behavior of elements between theγmatrix andγ′phase.The substitution of Co with Ni/Fe only slightly changes the type of precipitates on grain boundaries(GBs).The newly developed‘Co-free 282’low-cost alloys are not susceptible to stress-accelerated GB oxidation and exhibit great mechanical properties(tensile and creep),which are comparable to the 282 alloy.Current findings not only broaden the alloy selection for applications in extreme environments,but also represent an important trend in the field of precipitation-strengthened superalloys and high/medium entropy alloys to reduce the dependence on strategic high-cost metal Co.展开更多
Switchable polymerization is emerging as a powerful tool to construct block copolymers directly from mixtures of monomers.However,current achievements typically iterate between two polymerization cycles to afford prod...Switchable polymerization is emerging as a powerful tool to construct block copolymers directly from mixtures of monomers.However,current achievements typically iterate between two polymerization cycles to afford products with fixed sequences and compositions.Herein,we report the triethylborane/1,8-diazabicyclo[5.4.0]undec-7-ene(Et_3B/DBU)pair-mediated four-component switchable polymerization of propylene oxide(PO),CO_(2),phthalic anhydride(PA),and racemic lactide(rac-LA),which enables the on-demand synthesis of four different block copolymers,i.e.,poly(propylene phthalate)-b-polylactide(PPE-b-PLA),PPE-b-PLA-b-poly(propylene carbonate)(PPC),PPE-b-PPC-b-PLA,and PPE-b-PPCb-poly(propylene oxide)(PPO),through rationally modulating the Lewis pair(LP)ratio.Core to this protocol is that increasing the loading of Et_(3)B accelerates the ring-opening of PO while impeding the reactivity of rac-LA,thus allowing for fine-tuning of the thermodynamic and kinetic of the switchable polymerization.Therefore,the four polymerization cycles involving PO/PA ring-opening copolymerization(ROCOP),PO/CO_(2) ROCOP,rac-LA ring-opening polymerization(ROP),and PO ROP can be connected and discriminated in precisely programmed manners.展开更多
The article concluded that network pharmacology provides new ideas and insights into the molecular mechanism of traditional Chinese medicine(TCM)treatment of cancer.TCM is a new choice and hot spot in the field of can...The article concluded that network pharmacology provides new ideas and insights into the molecular mechanism of traditional Chinese medicine(TCM)treatment of cancer.TCM is a new choice and hot spot in the field of cancer treatment.We have also previously published studies on TCM and network pharmacology.In this letter,we summarize the new paradigm of network pharmacology in cancer treatment mechanisms.展开更多
Multicomponent(Hf-Zr-Ta)B_(2)potentially provides improved ablation resistance compared with silicon-based ceramics.Here we deposited(Hf_(0.5-x/2)Zr_(0.5-x/2)Ta_(x))B_(2)(x=0,0.1,and 0.2)coatings onto C/C com-posites,...Multicomponent(Hf-Zr-Ta)B_(2)potentially provides improved ablation resistance compared with silicon-based ceramics.Here we deposited(Hf_(0.5-x/2)Zr_(0.5-x/2)Ta_(x))B_(2)(x=0,0.1,and 0.2)coatings onto C/C com-posites,and investigated their ablation behaviors under an oxyacetylene torch with a heat flux of 2.4 MW m^(-2).It was observed that the x=0.1 oxide scale bulged but was denser,and the x=0.2 oxide scale was blown away due to the formation of excessive liquid.Based on these findings,we further de-veloped a duplex(Hf-Zr-Ta)B_(2)coating that showed a linear recession rate close to zero(0.11μm s^(-1))after two 120-s ablation cycles.It is identified that the resulting oxide scale is mainly composed of(Hf,Zr)_(6)Ta_(2)O_(17)and(Hf,Zr,Ta)O_(2)by performing aberration-corrected(scanning)transmission electron microscopy.The protective mechanism is related to the peritectic transformation of orthorhombic-(Hf,Zr)_(6)Ta_(2)O_(17)to tetragonal-(Hf,Zr,Ta)O_(2)plus Ta-dominated liquid.This study contributes to the develop-ment of Ta-containing multicomponent UHTC bulk and coatings for ultra-high temperature applications.展开更多
Novel hydrogen storage materials have propelled progress in hydrogen storage technologies.Magnesium hydride(MgH_(2))is a highly promising candidate.Nevertheless,several drawbacks,including the need for elevated therma...Novel hydrogen storage materials have propelled progress in hydrogen storage technologies.Magnesium hydride(MgH_(2))is a highly promising candidate.Nevertheless,several drawbacks,including the need for elevated thermal conditions,sluggish dehydrogena-tion kinetics,and high thermodynamic stability,limit its practical application.One effective method of addressing these challenges is cata-lyst doping,which effectively boosts the hydrogen storage capability of Mg-based materials.Herein,we review recent advancements in catalyst-doped MgH_(2) composites,with particular focus on multicomponent and high-entropy catalysts.Structure-property relationships and catalytic mechanisms in these doping strategies are also summarized.Finally,based on existing challenges,we discuss future research directions for the development of Mg-based hydrogen storage systems.展开更多
Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structur...Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structural studies of other physicochemical properties are con-ducted on a series of materials obtained by the sol-gel method with different ratios of Gd and Sm cations.It is documented that changing the x value,and the resulting adjustment of the average ionic radius,have a significant impact on the crystal structure,stability,as well as on the total conductivity and thermomechanical properties of the materials,with the best results obtained for the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)composition.Oxygen electrodes are prepared using the selected compound,allowing to obtain low polarization resistance values,such as 0.086Ω·cm^(2)at 800℃.Systematic studies of electrocatalytic activity are conducted using La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(_(0.2))O_(3−δ)as the electrolyte for all electrodes,and Ce_(0.8)Gd_(0.2)O_(2−δ)electrolyte for the best performing Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes.The electrochemical data are analyzed using the distribution of relaxation times method.Also,the influence of the preparation method of the electrode material is in-ve`stigated using the electrospinning technique.Finally,the performance of the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes is tested in a Ni-YSZ(yttria-stabilized zirconia)anode-supported cell with a Ce_(0.8)Gd_(0.2)O_(2−δ)buffer layer,in the fuel cell and electrolyzer operating modes.With the electrospun electrode,a power density of 462 mW·cm^(−2)is obtained at 700℃,with a current density of ca.0.2 A·cm^(−2)at 1.3 V for the electrolysis at the same temperature,indicating better performance compared to the sol-gel-based electrode.展开更多
A series of CeO_(2)@MnO_(2)composites was prepared by deposition-precipitation methods.These materials were used to activate sodium persulfate(PDS)for the oxidation of tetracycline.It is found that the composites,espe...A series of CeO_(2)@MnO_(2)composites was prepared by deposition-precipitation methods.These materials were used to activate sodium persulfate(PDS)for the oxidation of tetracycline.It is found that the composites,especially the CeO_(2)@MnO_(2)-1:4 composites,exhibit better tetracycline removal rates than the pure components.X-ray diffraction(XRD),Raman and scanning electron microscopy(SEM)analyses all indicate that the composite has been successfully prepared with high purity and high crystalline.The XPS analysis shows that the strong interaction between the components promotes the electron transfer.Additionally,the kinetic rate constants of CeO_(2)@MnO_(2)-1:4 after 60 min are 3.8 and 12.7 times higher than pure CeO_(2)and MnO_(2),respectively.CeO_(2)@MnO_(2-)1:4 composite also exhibits excellent catalytic activity for individual and hybrid pollutants.The effects of wastewater matrix,pH,circulation and ion stre ngth on the degradation of tetracycline were investigated.It is found that CeO_(2)@MnO_(2)-1:4 composite has good practical application prospects.CeO_(2)@MnO_(2)composites with synergistic adsorption catalysis can activate PDS and peroxymo no sulfate(PMS)for efficient organic catalytic oxidation.This paper provides the theoretical basis and data support for the practical application of the CeO_(2)@MnO_(2)composite materials.展开更多
Despite their attractive features of high energy density,low cost,and safety,polysulfide/iodide flow batteries(SIFBs)are hampered by the sluggish kinetics of the iodide redox couple,which restricts overall performance...Despite their attractive features of high energy density,low cost,and safety,polysulfide/iodide flow batteries(SIFBs)are hampered by the sluggish kinetics of the iodide redox couple,which restricts overall performance.Multicomponent sulfides are demonstrated as promising catalysts for accelerating I^(-)/I_(3)^(-) redox reactions.Concurrently,the enhanced configurational entropy arising from multinary compositions drives synergistic effects among constituent elements,establishing a viable pathway to optimize catalytic performance.Building on these foundations,this work introduces a targeted orbital hybridization-optimized electron density strategy to enhance the catalytic activity.Implementing this concept,we developed an in-situ solvothermal synthesis process for an entropy-enhanced AgCuZnSnS_(4) loaded graphite felt(ACZTS/GF)electrode.The engineered electrode demonstrates exceptional electrocatalytic performance with improved bulk conductivity and interfacial charge transfer kinetics within a SIFB.The cell achieves a high energy efficiency of 88.5%at 20 mA·cm^(−2) with 10%state-of-charge.Furthermore,the battery delivers a maximum power density of 119.8 mW·cm^(−2) and exhibits excellent long-term cycling stability.These significant results stem from orbital hybridization-driven electronic state optimization and entropy effect-induced synergistic catalysis.展开更多
Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes si...Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes since the concept of gut-brain axis(GBA)has been proposed.Here we present a microchip model co-culturing intestinal cells(Caco2),microbes(E.coli),and GBM cells(U87)to study inflammatory responses of GBM by investigating the tryptophan metabolism.E.coli after encapsulating with alginate hydrogel microparticles(AHMPs)was seeded in the microchip where Caco2 was located,forming the simulated system of intestinal physiology and avoiding excessive reproduction of microbes.Continuous flow was applied to maintain the cell viability,induce the morphogenesis,and simulate the tryptophan transportation in GBA.The morphological alterations of Caco2 and U87 were characterized by fluorescence imaging and the tryptophan metabolism,especially the tryptophan-kynurenine pathway,was analyzed by LC-MS.Above these results of molecular analysis and cell behavior,we can conclude that GBM inflammation is induced by tryptophan accumulation.This microchip-based model generally provides an alternative method for in vitro research of interactions in GBA.展开更多
Objectives:To assess the effects of a wearable-sensorassisted multicomponent exercise program on physical fitness,cognition and quality of life in a practical setting involving frail older adults.Methods:Frail older a...Objectives:To assess the effects of a wearable-sensorassisted multicomponent exercise program on physical fitness,cognition and quality of life in a practical setting involving frail older adults.Methods:Frail older adults(n=130)were randomly divided into a control(CG,n=68)group and an exercise group(EG,n=62)in a 12-week intervention,which included stride gait training with wearable sensors;aerobic exercise;and resistance,flexibility,balance,and cognitive training.Primary outcomes(physical fitness)were evaluated via the SPPB and SFT.Secondary outcomes(cognitive ability,quality of life and frailty)were evaluated via the MoCA-BC,SF-36 and Fried frailty criteria,respectively.Results:After the 12-week intervention,the EG demonstrated significant improvements(p<0.05)vs.the CG in gait speed(β_(3)=0.424,coefficient of interaction effect between group and time from the generalized linear mixed model),chair stand(β_(3)=0.501)and total score(β_(3)=65.466)of SPPB and all SFT components including 6MWT(walked distance,β_(3)=1.098;walking speed,β_(3)=0.105;stride length,β_(3)=0.041),back scratch(β_(3)=4.926),chair sit and reach(β_(3)=3.762),30s arm curl(β_(3)=6.124),30s sit-to-stand(β_(3)=3.04),and TUG(β_(3)=−6.712).The MoCA-BC total,verbal fluency and delayed recall scores;the physical function,general health,vitality,and mental health scores of the SF-36;and the frailty phenotype in the EG were significantly improved compared with those of the CG.Conclusions:The progressive wearable-sensor-assisted multicomponent exercise program designed in this study enhanced physical fitness,cognitive ability and quality of life and slowed down the progression of frailty in frail older adults,supporting its potential as a feasible communitybased health intervention.展开更多
We demonstrate a case study of Ce-doped yttrium aluminum garnet(YAG)phosphor to illustrate a novel plasma route for the synthesis of multicomponent materials with addressing morphology and structural control.The prese...We demonstrate a case study of Ce-doped yttrium aluminum garnet(YAG)phosphor to illustrate a novel plasma route for the synthesis of multicomponent materials with addressing morphology and structural control.The presented strategy was started directly from liquid precursors without any precipitating agents,and an innovative growth mechanism was proposed to explain the formation of monodispersed spherical particles with an adjusted size distribution.Homogeneous elemental distribution close to that of liquid precursors was also achieved due to the thermal nonequilibrium effect in plasma.Benefiting from the structural feature of the obtained product,a low transformation temperature of 1100℃for YAG phase was obtained and final products exhibit the highest photoluminescence intensity with rather low Ce doping of 0.5 wt.%,together with excellent thermal stability of 92%preservation of initial emission at 473 K.This work well illustrates the advance of plasma strategy in formation of multicomponent com-pounds with excellent performances,and its potential for large-scale production due to the transient and in-flight synthesis process.展开更多
Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great signif...Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great significance.In this work,trialdehydes,diamines,and trimethylsilyl cyanide could easily undergo multicomponent polymerization under mild conditions,producing hyperbranched poly(α-aminonitrile)s with high molecular weights(M_(w) up to 4.87×10^(4))in good yields(up to 85%).The hyperbranched poly(α-aminonitrile)s have good solubility in commonly used organic solvents,high thermal stability as well as morphological stability.Furthermore,due to the numerous aldehyde groups in their branched chains,these hb-poly(α-aminonitrile)s can undergo one-pot,two-step,four-component post-polymerization with high efficiency.This work not only confirms the efficiency of our established catalyst-free multicomponent polymerization of aldehydes,amines and trimethylsilyl cyanide,but also provides a versatile and powerful platform for the preparation of functional hyperbranched polymeric materials.展开更多
This study reports the response of helium(He)ion irradiation on binary-phase structured alloy V_(34)Ti_(25)Cr_(10)Ni_(30)Pd1.The alloy consists of a VCr matrix with nano-sized TiNi precipitates and a B2 TiNi matrix wi...This study reports the response of helium(He)ion irradiation on binary-phase structured alloy V_(34)Ti_(25)Cr_(10)Ni_(30)Pd1.The alloy consists of a VCr matrix with nano-sized TiNi precipitates and a B2 TiNi matrix with nano-sized VCr precipitates.VCr is chemical-disordered and TiNi has a B2-ordered structure.The alloy was subjected to 400 keV He ion irradiation with a fluence of 1×10^(17)ions cm^(−2)at 450℃.The results show He bubbles within the chemical-disordered VCr matrix exhibit a near-spherical shape with a smaller size and higher density compared to that in chemical-ordered TiNi phase with a larger size,lower density,and faceted shape.This indicates the chemical-disordered VCr phase effectively suppresses He accumulation compared to the B2-ordered TiNi phase,emphasizing the dominance of chemical struc-tures in He bubble formation.The calculation of density functional theory(DFT)shows that Ti and Ni have lower vacancy formation energy than that of V and Cr,respectively,which results in the increased vacancy production in TiNi.Consequently,He bubbles in TiNi have a larger bubble size consistent with experimental observations of radiation-induced Ni segregation.These findings elucidate the roles of or-dered and disordered chemical structures in He bubble evolution,offering insights for the development of gas ion irradiation-resistant materials.展开更多
Premature adiabatic shear localization caused by strain softening is a roadblock for the application of body-centered cubic(BCC)structured high-entropy alloy(HEAs)in the impact field.A micron-scale orthorhombic-phase(...Premature adiabatic shear localization caused by strain softening is a roadblock for the application of body-centered cubic(BCC)structured high-entropy alloy(HEAs)in the impact field.A micron-scale orthorhombic-phase(O-phase)strengthened TiZrVNbAl alloy was developed to delay adiabatic shear failure and enhance dynamic ductility.The O-phase can not only reduce the slip length,but also promote the pinning and tangling of the dislocations near the phase boundaries.The introduction of the O-phase transformed the strain hardening rate from negative to positive,resulting in a significantly improved dynamic shear resistance.Meanwhile,slip transfer across the O-phase via dislocation cutting mechanisms and a reduction of slip band spacing guaranteed dynamic deformation uniformity.Benefiting from the introduction of the O-phase,the alloy exhibits an excellent stored energy density(∼446 J/cm^(3),surpass the reported BCC-HEAs and typical titanium alloys),a large dynamic fracture strain(∼42%)and a considerable dynamic specific yield strength(∼241 MPa cm^(3)g^(-1)).The present study presents an effective approach for developing BCC-HEAs with excellent dynamic shear resistance and plasticity.展开更多
Exploration of new green polymerization strategies for the construction of conjugated polymers is important but challengeable.In this work,a multicomponent polymerization of acetylarenes,alkynones and ammonium acetate...Exploration of new green polymerization strategies for the construction of conjugated polymers is important but challengeable.In this work,a multicomponent polymerization of acetylarenes,alkynones and ammonium acetate for in situ construction of conjugated poly(triarylpyridine)s was developed.The polymerization reactions of diacetylarenes,aromatic dialkynones and NH_(4)OAc were performed in dimethylsulfoxide(DMSO)under heating in the presence of potassium tert-butoxide(t-BuOK),affording four conjugated poly(2,4,6-triarylpyridine)s(PTAPs)in satisfactory yields.The resulting PTAPs have good solubility in common organic solvents and high thermal stability with 5%weight loss temperatures reaching up to 460℃.They are also electrochemically active.The PTAPs incorporating tetraphenylethene units manifest aggregation-induced emission features.Moreover,through simply being doped into poly(vinyl alcohol)(PVA)matrix,the polymer and model compound containing triphenylamine moieties exhibit room-temperature phosphorescence properties with ultralong lifetimes up to 696.2 ms and high quantum yields up to 28.7%.This work not only provides a facile green synthetic route for conjugated polymers but also offers new insights into the design of advanced materials with unique photophysical properties.展开更多
基金the National Natural Science Foundation of China(Grant No.81872996)the State Key Research and Development Project(Grant No.2017YFC1702104)+1 种基金the State Key Project for the Creation of Major New Drugs(2018ZX09711001-009-010)the Tianjin Municipal Education Commission Research Project(Grant No.2017ZD07)。
文摘Inherent complexity of plant metabolites necessitates the use of multi-dimensional information to accomplish comprehensive profiling and confirmative identification.A dimension-enhanced strategy,by offline two-dimensional liquid chromatography/ion mobility-quadrupole time-of-flight mass spectrometry(2 D-LC/IM-QTOF-MS)enabling four-dimensional separations(2 D-LC,IM,and MS),is proposed.In combination with in-house database-driven automated peak annotation,this strategy was utilized to characterize ginsenosides simultaneously from white ginseng(WG)and red ginseng(RG).An offline 2 DLC system configuring an Xbridge Amide column and an HSS T3 column showed orthogonality 0.76 in the resolution of ginsenosides.Ginsenoside analysis was performed by data-independent high-definition MSE(HDMSE)in the negative ESI mode on a Vion?IMS-QTOF hybrid high-resolution mass spectrometer,which could better resolve ginsenosides than MSEand directly give the CCS information.An in-house ginsenoside database recording 504 known ginsenosides and 58 reference compounds,was established to assist the identification of ginsenosides.Streamlined workflows,by applying UNIFI?to automatedly annotate the HDMSEdata,were proposed.We could separate and characterize 323 ginsenosides(including 286 from WG and 306 from RG),and 125 thereof may have not been isolated from the Panax genus.The established 2 D-LC/IM-QTOF-HDMSEapproach could also act as a magnifier to probe differentiated components between WG and RG.Compared with conventional approaches,this dimensionenhanced strategy could better resolve coeluting herbal components and more efficiently,more reliably identify the multicomponents,which,we believe,offers more possibilities for the systematic exposure and confirmative identification of plant metabolites.
基金financially supported by the National Natural Science Foundation of China(21773247,21521061,21875252)the Natural Science Foundation of Fujian Province(2006L2005).
文摘Developing a new strategy for the synthesis of high-nuclear transition metal(TM)cluster substituted polyoxometalates(POMs)provides an avenue for new materials with unique functions.Herein,the synergetic coordination strategy of 1,2,4-1H-triazole(Htrz),ethylenediamine(en),and a lacunary POM was applied to construct a highnuclear Ni cluster substituted POM.As a result,a{Ni_(30)}cluster substituted POM,[Ni(trz)3]2@[Ni_(30)(H2O)16]POM.
基金supported by the National Natural Science Foundation of China(No.22431004)Fund of Guangdong Provincial Key Laboratory of Luminescence from Molecular Aggregates(No.2023B1212060003)。
文摘Aggregation-induced emission(AIE)polymers have been extensively studied;however,the integration of AIE units into polyelectrolytes remains largely limited by the laborious multistep synthesis of pre-designed emissive monomers.Herein,we report a one-pot multicomponent polymerization method that directly produces main-chain charged polyelectrolytes with intrinsic AIE characteristics from non-emissive building blocks.By optimizing the monomer structures and reaction conditions,a series of soluble high-molecular-weight polymers with welldefined backbones were obtained in high yields.The resulting polyelectrolytes displayed robust AIE behavior,exhibiting fluorescence enhancement up to about 60-fold in an aqueous environment,and maintained excellent thermal stability.Owing to their cationic backbones,these polymers interact strongly with microbial surfaces and exhibit remarkable antimicrobial activities.This study establishes a synthetically efficient route to AIE polyelectrolytes and highlights their potential applications as multifunctional materials for bioimaging,antimicrobial therapy,and other applications.
基金supported by the National Natural Science Foundation of China(No.U2330110)Youth Science Foundation Project(Category A)of Liaoning Province,China(No.2025JH6/101100006).
文摘This study investigates the microstructure and co-precipitation behavior of multicomponent(Ni(Al,Mn)and Cu)nanoparticles in the weld heat-affected zones of high-strength low-carbon steel.Through thermal simulations,the intercritical,fine-grained,and coarsegrained heat-affected zones were systematically characterized to elucidate the interplay between the microstructure,precipitation,and mechanical properties.At a heat input of 30 kJ·cm^(−1),Ni(Al,Mn)nanoparticles dissolve in the intercritical heat-affected zone,followed by dense reprecipitation coupled with significant coarsening of Cu particles during cooling,thereby retaining high strength but reducing impact toughness to(142±10)J(compared to(205±8)J of the base metal).The fine-grained heat-affected zone,under the same heat input,exhibits a refined ferritic-bainite matrix with a few fine Ni(Al,Mn)and slightly coarsened Cu particles,thus enhancing plastic deformation capacity and resulting in superior impact toughness of(196±7)J.Despite complete dissolution of original precipitates at peak temperatures in the coarse-grained heat-affected zone,re-precipitated nanoparticles provide effective strengthening effect,compensating for grain coarsening and dislocation recovery and resulting in an impressive impact toughness of(186±6)J.The toughening mechanism is primarily attributed to the synergistic actions of the matrix,precipitates,and deformation twins.These findings provide mechanistic and quantitative insights for developing processing-microstructure-property relationships in different welding heat-affected zones,and this framework can be further utilized to optimize welding parameters for tailored applications.
基金financially supported by the National Key Research and Development Project of China(No.2022YFB3806900)。
文摘The complex interactions and conflicting performance demands in multi-component composites pose significant challenges for achieving balanced multi-property optimization through conventional trial-and-error approaches.Machine learning(ML)offers a promising solution,markedly improving materials discovery efficiency.However,the high dimensionality of feature spaces in such systems has long impeded effective ML-driven feature representation and inverse design.To overcome this,we present an Intelligent Screening System(ISS)framework to accelerate the discovery of optimal formulations balancing four key properties in 15-component PTFE-based copper-clad laminate composites(PTFE-CCLCs).ISS adopts modular descriptors based on the physical information of component volume fractions,thereby simplifying the feature representation.By leveraging the inverse prediction capability of ML models and constructing a performance-driven virtual candidate database,ISS significantly reduced the computational complexity associated with high-dimensional spaces.Experimental validation confirmed that ISSoptimized formulations exhibited superior synergy,notably resolving the trade-off between thermal conductivity and peel strength,and outperform many commercial counterparts.Despite limited data and inherent process variability,ISS achieved an average prediction accuracy of 76.5%,with thermal conductivity predictions exceeding 90%,demonstrating robust reliability.This work provides an innovative,efficient strategy for multifunctional optimization and accelerated discovery in ultra-complex composite systems,highlighting the integration of ML and advanced materials design.
基金supported by the National Natural Science Foundation of China(Grant Nos.52471019 and 52571019)the Zhejiang Provincial Natural Science Foundation of China under Grant No.LR24E010001.
文摘The development of a new precipitation-strengthened Ni-based superalloy relies on a seemingly contradictory yet crucial trade-off between‘easy-to-deform’and‘high strength’.Commercial Haynes 282(Ni-20Cr-10Co-8.5Mo-2.1Ti-1.5Al)has a good balance of mechanical properties and formability,but it still faces growing concerns regarding material cost and applicability due to the high concentration of Co(∼10 wt%).Therefore,it is necessary to develop Co-free,easy-to-deform and low-cost alloys with thermomechanical processing capabilities and mechanical properties comparable to those of Haynes 282.Both Ni and Fe are selected to replace Co,because the atomic sizes of Fe,Ni and Co are almost identical(∼0.125 nm).Moreover,the moduli of Co and Fe are all 82 GPa,which is only 7%higher than that of Ni(76 GPa).The effects of Co substitution by Ni/Fe on the alloy microstructures and mechanical properties are investigated.Substitution of Co with Ni/Fe does not change the size and volume fraction of theγ′phase,nor does it change the partitioning behavior of elements between theγmatrix andγ′phase.The substitution of Co with Ni/Fe only slightly changes the type of precipitates on grain boundaries(GBs).The newly developed‘Co-free 282’low-cost alloys are not susceptible to stress-accelerated GB oxidation and exhibit great mechanical properties(tensile and creep),which are comparable to the 282 alloy.Current findings not only broaden the alloy selection for applications in extreme environments,but also represent an important trend in the field of precipitation-strengthened superalloys and high/medium entropy alloys to reduce the dependence on strategic high-cost metal Co.
基金financially supported by National Key R&D Program Young Scientists Project(No.2023YFC3903100)the National Natural Science Foundation of China(No.22322503)analytical and testing assistance from the Analysis and Testing Center of HUST。
文摘Switchable polymerization is emerging as a powerful tool to construct block copolymers directly from mixtures of monomers.However,current achievements typically iterate between two polymerization cycles to afford products with fixed sequences and compositions.Herein,we report the triethylborane/1,8-diazabicyclo[5.4.0]undec-7-ene(Et_3B/DBU)pair-mediated four-component switchable polymerization of propylene oxide(PO),CO_(2),phthalic anhydride(PA),and racemic lactide(rac-LA),which enables the on-demand synthesis of four different block copolymers,i.e.,poly(propylene phthalate)-b-polylactide(PPE-b-PLA),PPE-b-PLA-b-poly(propylene carbonate)(PPC),PPE-b-PPC-b-PLA,and PPE-b-PPCb-poly(propylene oxide)(PPO),through rationally modulating the Lewis pair(LP)ratio.Core to this protocol is that increasing the loading of Et_(3)B accelerates the ring-opening of PO while impeding the reactivity of rac-LA,thus allowing for fine-tuning of the thermodynamic and kinetic of the switchable polymerization.Therefore,the four polymerization cycles involving PO/PA ring-opening copolymerization(ROCOP),PO/CO_(2) ROCOP,rac-LA ring-opening polymerization(ROP),and PO ROP can be connected and discriminated in precisely programmed manners.
文摘The article concluded that network pharmacology provides new ideas and insights into the molecular mechanism of traditional Chinese medicine(TCM)treatment of cancer.TCM is a new choice and hot spot in the field of cancer treatment.We have also previously published studies on TCM and network pharmacology.In this letter,we summarize the new paradigm of network pharmacology in cancer treatment mechanisms.
基金supported by the National Key R&D Pro-gram of China(Grant No.2021YFA0715803)the National Natural Science Foundation of China(Grant Nos.52293373,52130205,and 52302091)+1 种基金the Joint Fund of Henan Province Science and Technol-ogy R&D Program(No.225200810002)the ND Basic Research Funds of Northwestern Polytechnical University(No.G2022WD).
文摘Multicomponent(Hf-Zr-Ta)B_(2)potentially provides improved ablation resistance compared with silicon-based ceramics.Here we deposited(Hf_(0.5-x/2)Zr_(0.5-x/2)Ta_(x))B_(2)(x=0,0.1,and 0.2)coatings onto C/C com-posites,and investigated their ablation behaviors under an oxyacetylene torch with a heat flux of 2.4 MW m^(-2).It was observed that the x=0.1 oxide scale bulged but was denser,and the x=0.2 oxide scale was blown away due to the formation of excessive liquid.Based on these findings,we further de-veloped a duplex(Hf-Zr-Ta)B_(2)coating that showed a linear recession rate close to zero(0.11μm s^(-1))after two 120-s ablation cycles.It is identified that the resulting oxide scale is mainly composed of(Hf,Zr)_(6)Ta_(2)O_(17)and(Hf,Zr,Ta)O_(2)by performing aberration-corrected(scanning)transmission electron microscopy.The protective mechanism is related to the peritectic transformation of orthorhombic-(Hf,Zr)_(6)Ta_(2)O_(17)to tetragonal-(Hf,Zr,Ta)O_(2)plus Ta-dominated liquid.This study contributes to the develop-ment of Ta-containing multicomponent UHTC bulk and coatings for ultra-high temperature applications.
基金financially supported by the National Key Research and Development Program of China (No. 2021YFB4000604)the National Natural Science Foundation of China (No. 52271220)+2 种基金the 111 Project (No. B12015)the Fundamental Research Funds for the Central UniversitiesHaihe Laboratory of Sustainable Chemical Transformations, Guangxi Collaborative Innovation Centre of Structure and Property for New Energy and Materials, Science Research and Technology Development Project of Guilin (No. 20210102-4)
文摘Novel hydrogen storage materials have propelled progress in hydrogen storage technologies.Magnesium hydride(MgH_(2))is a highly promising candidate.Nevertheless,several drawbacks,including the need for elevated thermal conditions,sluggish dehydrogena-tion kinetics,and high thermodynamic stability,limit its practical application.One effective method of addressing these challenges is cata-lyst doping,which effectively boosts the hydrogen storage capability of Mg-based materials.Herein,we review recent advancements in catalyst-doped MgH_(2) composites,with particular focus on multicomponent and high-entropy catalysts.Structure-property relationships and catalytic mechanisms in these doping strategies are also summarized.Finally,based on existing challenges,we discuss future research directions for the development of Mg-based hydrogen storage systems.
基金funded by the National Science Centre,Poland,on the basis of the decision number UMO-2020/37/B/ST8/02097supported by the program“Excellence Initiative-Research University”for the AGH University of Krakow(IDUB AGH,No.501.696.7996,Action 4,ID 9880).
文摘Multicomponent Gd_(1−x)Sm_(x)Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)double perovskites are optimized for application in terms of chemical composi-tion and morphology for the use as oxygen electrodes in solid oxide cells.Structural studies of other physicochemical properties are con-ducted on a series of materials obtained by the sol-gel method with different ratios of Gd and Sm cations.It is documented that changing the x value,and the resulting adjustment of the average ionic radius,have a significant impact on the crystal structure,stability,as well as on the total conductivity and thermomechanical properties of the materials,with the best results obtained for the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)composition.Oxygen electrodes are prepared using the selected compound,allowing to obtain low polarization resistance values,such as 0.086Ω·cm^(2)at 800℃.Systematic studies of electrocatalytic activity are conducted using La_(0.8)Sr_(0.2)Ga_(0.8)Mg_(_(0.2))O_(3−δ)as the electrolyte for all electrodes,and Ce_(0.8)Gd_(0.2)O_(2−δ)electrolyte for the best performing Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes.The electrochemical data are analyzed using the distribution of relaxation times method.Also,the influence of the preparation method of the electrode material is in-ve`stigated using the electrospinning technique.Finally,the performance of the Gd_(0.75)Sm_(0.2)5Ba_(0.5)Sr_(0.5)CoCuO_(5+δ)electrodes is tested in a Ni-YSZ(yttria-stabilized zirconia)anode-supported cell with a Ce_(0.8)Gd_(0.2)O_(2−δ)buffer layer,in the fuel cell and electrolyzer operating modes.With the electrospun electrode,a power density of 462 mW·cm^(−2)is obtained at 700℃,with a current density of ca.0.2 A·cm^(−2)at 1.3 V for the electrolysis at the same temperature,indicating better performance compared to the sol-gel-based electrode.
基金Project supported by the Science and Technology Project of Henan Province(242102321048,242102321045,232102320211)National Natural Science Foundation of China(22206080)+2 种基金Natural Science Foundation of Jiangsu(SBK2022041070)International Science and Technology Cooperation Projects of Henan Province(232102521009)Natural Science Youth Foundation of Henan Province(232300420336)。
文摘A series of CeO_(2)@MnO_(2)composites was prepared by deposition-precipitation methods.These materials were used to activate sodium persulfate(PDS)for the oxidation of tetracycline.It is found that the composites,especially the CeO_(2)@MnO_(2)-1:4 composites,exhibit better tetracycline removal rates than the pure components.X-ray diffraction(XRD),Raman and scanning electron microscopy(SEM)analyses all indicate that the composite has been successfully prepared with high purity and high crystalline.The XPS analysis shows that the strong interaction between the components promotes the electron transfer.Additionally,the kinetic rate constants of CeO_(2)@MnO_(2)-1:4 after 60 min are 3.8 and 12.7 times higher than pure CeO_(2)and MnO_(2),respectively.CeO_(2)@MnO_(2-)1:4 composite also exhibits excellent catalytic activity for individual and hybrid pollutants.The effects of wastewater matrix,pH,circulation and ion stre ngth on the degradation of tetracycline were investigated.It is found that CeO_(2)@MnO_(2)-1:4 composite has good practical application prospects.CeO_(2)@MnO_(2)composites with synergistic adsorption catalysis can activate PDS and peroxymo no sulfate(PMS)for efficient organic catalytic oxidation.This paper provides the theoretical basis and data support for the practical application of the CeO_(2)@MnO_(2)composite materials.
基金supported by the National Natural Science Foundation of China(Nos.22171180,22461142137,and 22478242)the Shanghai Municipal Science and Technology Major Project,China.
文摘Despite their attractive features of high energy density,low cost,and safety,polysulfide/iodide flow batteries(SIFBs)are hampered by the sluggish kinetics of the iodide redox couple,which restricts overall performance.Multicomponent sulfides are demonstrated as promising catalysts for accelerating I^(-)/I_(3)^(-) redox reactions.Concurrently,the enhanced configurational entropy arising from multinary compositions drives synergistic effects among constituent elements,establishing a viable pathway to optimize catalytic performance.Building on these foundations,this work introduces a targeted orbital hybridization-optimized electron density strategy to enhance the catalytic activity.Implementing this concept,we developed an in-situ solvothermal synthesis process for an entropy-enhanced AgCuZnSnS_(4) loaded graphite felt(ACZTS/GF)electrode.The engineered electrode demonstrates exceptional electrocatalytic performance with improved bulk conductivity and interfacial charge transfer kinetics within a SIFB.The cell achieves a high energy efficiency of 88.5%at 20 mA·cm^(−2) with 10%state-of-charge.Furthermore,the battery delivers a maximum power density of 119.8 mW·cm^(−2) and exhibits excellent long-term cycling stability.These significant results stem from orbital hybridization-driven electronic state optimization and entropy effect-induced synergistic catalysis.
基金supported by the National Key R&D Program of China(No.2021YFF0600700)the National Natural Science Foundation of China(No.22034005)+1 种基金Research Projects of Putian University(No.2024172)the Startup Fund for Advanced Talents of Putian University(No.2024046)。
文摘Inflammation is often accompanied by glioblastoma cells(GBMs)and is considered a key factor for GBM growth.This feature is believed to be connected with the tryptophan pathway mainly affected by intestinal microbes since the concept of gut-brain axis(GBA)has been proposed.Here we present a microchip model co-culturing intestinal cells(Caco2),microbes(E.coli),and GBM cells(U87)to study inflammatory responses of GBM by investigating the tryptophan metabolism.E.coli after encapsulating with alginate hydrogel microparticles(AHMPs)was seeded in the microchip where Caco2 was located,forming the simulated system of intestinal physiology and avoiding excessive reproduction of microbes.Continuous flow was applied to maintain the cell viability,induce the morphogenesis,and simulate the tryptophan transportation in GBA.The morphological alterations of Caco2 and U87 were characterized by fluorescence imaging and the tryptophan metabolism,especially the tryptophan-kynurenine pathway,was analyzed by LC-MS.Above these results of molecular analysis and cell behavior,we can conclude that GBM inflammation is induced by tryptophan accumulation.This microchip-based model generally provides an alternative method for in vitro research of interactions in GBA.
基金supported by the project of Guangzhou Sports Science and Technology Collaborative Innovation Center(No.SL2022B04J00034)National Key Research and Development Program of China(No.2020YFC2002900)。
文摘Objectives:To assess the effects of a wearable-sensorassisted multicomponent exercise program on physical fitness,cognition and quality of life in a practical setting involving frail older adults.Methods:Frail older adults(n=130)were randomly divided into a control(CG,n=68)group and an exercise group(EG,n=62)in a 12-week intervention,which included stride gait training with wearable sensors;aerobic exercise;and resistance,flexibility,balance,and cognitive training.Primary outcomes(physical fitness)were evaluated via the SPPB and SFT.Secondary outcomes(cognitive ability,quality of life and frailty)were evaluated via the MoCA-BC,SF-36 and Fried frailty criteria,respectively.Results:After the 12-week intervention,the EG demonstrated significant improvements(p<0.05)vs.the CG in gait speed(β_(3)=0.424,coefficient of interaction effect between group and time from the generalized linear mixed model),chair stand(β_(3)=0.501)and total score(β_(3)=65.466)of SPPB and all SFT components including 6MWT(walked distance,β_(3)=1.098;walking speed,β_(3)=0.105;stride length,β_(3)=0.041),back scratch(β_(3)=4.926),chair sit and reach(β_(3)=3.762),30s arm curl(β_(3)=6.124),30s sit-to-stand(β_(3)=3.04),and TUG(β_(3)=−6.712).The MoCA-BC total,verbal fluency and delayed recall scores;the physical function,general health,vitality,and mental health scores of the SF-36;and the frailty phenotype in the EG were significantly improved compared with those of the CG.Conclusions:The progressive wearable-sensor-assisted multicomponent exercise program designed in this study enhanced physical fitness,cognitive ability and quality of life and slowed down the progression of frailty in frail older adults,supporting its potential as a feasible communitybased health intervention.
基金supported by the National Natu-ral Science Foundation of China(No.52174342)the Beijing Nat-ural Science Foundation(No.2232044)the Beijing Munic-ipal Education Commission Research Plan General Project(No.KM202410005009).
文摘We demonstrate a case study of Ce-doped yttrium aluminum garnet(YAG)phosphor to illustrate a novel plasma route for the synthesis of multicomponent materials with addressing morphology and structural control.The presented strategy was started directly from liquid precursors without any precipitating agents,and an innovative growth mechanism was proposed to explain the formation of monodispersed spherical particles with an adjusted size distribution.Homogeneous elemental distribution close to that of liquid precursors was also achieved due to the thermal nonequilibrium effect in plasma.Benefiting from the structural feature of the obtained product,a low transformation temperature of 1100℃for YAG phase was obtained and final products exhibit the highest photoluminescence intensity with rather low Ce doping of 0.5 wt.%,together with excellent thermal stability of 92%preservation of initial emission at 473 K.This work well illustrates the advance of plasma strategy in formation of multicomponent com-pounds with excellent performances,and its potential for large-scale production due to the transient and in-flight synthesis process.
基金financially supported by the Scientific Research Start-up Fund Project of Anhui Polytechnic University for Introducing Talents(No.2022YQQ081)Natural Science Research Project of Anhui Educational Committee(No.2024AH050133)the National Natural Science Foundation of China(No.22001078).
文摘Functional hyperbranched polymers,as an important class of materials,are widely applied in diverse areas.Therefore,the development of simple and efficient reactions to prepare hyperbranched polymers is of great significance.In this work,trialdehydes,diamines,and trimethylsilyl cyanide could easily undergo multicomponent polymerization under mild conditions,producing hyperbranched poly(α-aminonitrile)s with high molecular weights(M_(w) up to 4.87×10^(4))in good yields(up to 85%).The hyperbranched poly(α-aminonitrile)s have good solubility in commonly used organic solvents,high thermal stability as well as morphological stability.Furthermore,due to the numerous aldehyde groups in their branched chains,these hb-poly(α-aminonitrile)s can undergo one-pot,two-step,four-component post-polymerization with high efficiency.This work not only confirms the efficiency of our established catalyst-free multicomponent polymerization of aldehydes,amines and trimethylsilyl cyanide,but also provides a versatile and powerful platform for the preparation of functional hyperbranched polymeric materials.
基金supported by the National Magnetic Con-finement Fusion Energy Research Project from the Ministry of Science and Technology of China(No.2022YFE03030004 and 2019YFE03120003)the National Natural Science Foundation of China(No.12275010,12275176,12275001,12335017,11921006,U21B2082,U22B2064 and U20B2025)+3 种基金the Beijing Municipal Natural Science Foundation(No.1222023)the Shenzhen Science and Technology Program(No.RCYX20210609103904028)Engang Fu acknowledges the support from the Science Fund or Creative Research Groups of NSFC,the Ion Beam Materials Laboratory(IBML)and Electron Microscopy Laboratory(EML)the High-performance Computing Platform(HPC)at Peking University.Xing Liu acknowledges the discussion with Prof.Ning Gao and Dr.Yifan Zhang.
文摘This study reports the response of helium(He)ion irradiation on binary-phase structured alloy V_(34)Ti_(25)Cr_(10)Ni_(30)Pd1.The alloy consists of a VCr matrix with nano-sized TiNi precipitates and a B2 TiNi matrix with nano-sized VCr precipitates.VCr is chemical-disordered and TiNi has a B2-ordered structure.The alloy was subjected to 400 keV He ion irradiation with a fluence of 1×10^(17)ions cm^(−2)at 450℃.The results show He bubbles within the chemical-disordered VCr matrix exhibit a near-spherical shape with a smaller size and higher density compared to that in chemical-ordered TiNi phase with a larger size,lower density,and faceted shape.This indicates the chemical-disordered VCr phase effectively suppresses He accumulation compared to the B2-ordered TiNi phase,emphasizing the dominance of chemical struc-tures in He bubble formation.The calculation of density functional theory(DFT)shows that Ti and Ni have lower vacancy formation energy than that of V and Cr,respectively,which results in the increased vacancy production in TiNi.Consequently,He bubbles in TiNi have a larger bubble size consistent with experimental observations of radiation-induced Ni segregation.These findings elucidate the roles of or-dered and disordered chemical structures in He bubble evolution,offering insights for the development of gas ion irradiation-resistant materials.
基金supported by the YEQISUN Joint Funds of the National Natural Science Foundation of China(Grant No.U2241234)the National Natural Science Foundation of China(Grant No.52301127).
文摘Premature adiabatic shear localization caused by strain softening is a roadblock for the application of body-centered cubic(BCC)structured high-entropy alloy(HEAs)in the impact field.A micron-scale orthorhombic-phase(O-phase)strengthened TiZrVNbAl alloy was developed to delay adiabatic shear failure and enhance dynamic ductility.The O-phase can not only reduce the slip length,but also promote the pinning and tangling of the dislocations near the phase boundaries.The introduction of the O-phase transformed the strain hardening rate from negative to positive,resulting in a significantly improved dynamic shear resistance.Meanwhile,slip transfer across the O-phase via dislocation cutting mechanisms and a reduction of slip band spacing guaranteed dynamic deformation uniformity.Benefiting from the introduction of the O-phase,the alloy exhibits an excellent stored energy density(∼446 J/cm^(3),surpass the reported BCC-HEAs and typical titanium alloys),a large dynamic fracture strain(∼42%)and a considerable dynamic specific yield strength(∼241 MPa cm^(3)g^(-1)).The present study presents an effective approach for developing BCC-HEAs with excellent dynamic shear resistance and plasticity.
基金supported by the National Natural Science Foundation of China(No.22071166)the Priority Academic Program Development of Jiangsu High Education Institutions(PAPD).
文摘Exploration of new green polymerization strategies for the construction of conjugated polymers is important but challengeable.In this work,a multicomponent polymerization of acetylarenes,alkynones and ammonium acetate for in situ construction of conjugated poly(triarylpyridine)s was developed.The polymerization reactions of diacetylarenes,aromatic dialkynones and NH_(4)OAc were performed in dimethylsulfoxide(DMSO)under heating in the presence of potassium tert-butoxide(t-BuOK),affording four conjugated poly(2,4,6-triarylpyridine)s(PTAPs)in satisfactory yields.The resulting PTAPs have good solubility in common organic solvents and high thermal stability with 5%weight loss temperatures reaching up to 460℃.They are also electrochemically active.The PTAPs incorporating tetraphenylethene units manifest aggregation-induced emission features.Moreover,through simply being doped into poly(vinyl alcohol)(PVA)matrix,the polymer and model compound containing triphenylamine moieties exhibit room-temperature phosphorescence properties with ultralong lifetimes up to 696.2 ms and high quantum yields up to 28.7%.This work not only provides a facile green synthetic route for conjugated polymers but also offers new insights into the design of advanced materials with unique photophysical properties.
