The future large-scale application of sodium-ion batteries(SIBs)is inseparable from their excellent electrochemical performance and reliable safety characteristics.At present,there are few studies focusing on their sa...The future large-scale application of sodium-ion batteries(SIBs)is inseparable from their excellent electrochemical performance and reliable safety characteristics.At present,there are few studies focusing on their safety performance.The analysis of thermal stability and structural changes within a single material cannot systematically describe the complex interplay of components within the battery system during the thermal runaway process.Furthermore,the reaction between the battery materials themselves and their counterparts within the system can stimulate more intense exothermic behavior,thereby affecting the safety of the entire battery system.Therefore,this study delved into the thermal generation and gas evolution characteristics of the positive electrode(Na_(x)Ni_(1/3)Fe_(1/3)Mn_(1/3)O_(2),NFM111)and the negative electrode(hard carbon,HC)in SIBs,utilizing various material combinations.Through the integration of microscopic and macroscopic characterization techniques,the underlying reaction mechanisms of the positive and negative electrode materials within the battery during the heating process were elucidated.Three important results are derived from this study:(Ⅰ)The instability of the solid electrolyte interphase(SEI)leads to its decomposition at temperatures below 100℃,followed by extensive decomposition within the range of 100-150℃,yielding heat and the formation of inorganic compounds,such as Na_(2)CO_(3)and Na_(2)O;(Ⅱ)The reaction between NFM111 and the electrolyte constitutes the primary exothermic event during thermal abuse,with a discernible reaction also occurring between sodium metal and the electrolyte throughout the heating process;(Ⅲ)The heat production and gas generation behaviors of multi-component reactions do not exhibit complete correlation,and the occurrence of gas production does not necessarily coincide with thermal behavior.The results presented in this study can provide useful guidance for the safety improvement of SIBs.展开更多
Thermal quenching(TQ)at elevated temperature is a major factor affecting the luminescent intensity and efficiency of phosphors.Improving the thermal stability of phosphors and weakening the TQ effect are of significan...Thermal quenching(TQ)at elevated temperature is a major factor affecting the luminescent intensity and efficiency of phosphors.Improving the thermal stability of phosphors and weakening the TQ effect are of significance for the high-quality illumination of phosphor-converted WLEDs.Here,a novel red-emitting phosphor K_(2)Zn(PO_(3))_(4)∶Mn^(2+)is synthesized by standard high temperature solid state reaction in ambient atmosphere,which is a new member of self-reduction system.An effective synthesis strategy is proposed to optimize its photoluminescent performances.Combined with X-ray photoelectron spectroscopy and X-ray absorption fine structure spectroscopy,oxygen vacancy defects introduced by Mn doping are proved to play an important role in the transition of Mn^(4+)→Mn^(2+).Thermoluminescence analysis reveals that the distribution of trap levels,especially the deep ones,is effectively regulated by the controllable crystallization and significantly affect the thermal stability of phosphors.Then a defect-assisted model is proposed to address the inner mechanism of the phenomenon.The carriers trapped by deep trap levels can be released under the high-temperature stimulus,which return back to the luminescent centers and participate in the radiative recombination to improve thermal stability.This study provides a new crystallographic idea and theoretical support for obtaining luminescent materials with high thermal stability.展开更多
A novel oxide-dispersion-strengthened(ODS)die steel was fabricated by mechanical alloying and hot consolidation.Annealing and quench-tempering treatments both obtained an ultra-fine grain structure(mean size:310-330 n...A novel oxide-dispersion-strengthened(ODS)die steel was fabricated by mechanical alloying and hot consolidation.Annealing and quench-tempering treatments both obtained an ultra-fine grain structure(mean size:310-330 nm)with an ultra-high density of ultra-fine Y-Al-O nano-oxides(number density:~(1-1.5)×10^(23)m^(−3),mean size:5.1-7.2 nm).Prolonged thermal exposure further induced the new,highly dense precipitation of ultra-fine Y-Zr-O nano-oxides.Both nano-oxides tended to be wrapped up with a B2-NiAl nano-shells.Although the quench-tempered sample showed much higher room-temperature strength(yield strength=1393±40 MPa and ultimate tensile strength=1774±11 MPa)and slightly lower elongation(elongation=13.6%±0.6%)than the annealed sample(YS=988±7 MPa,UTS=1490±12 MPa,and EL=15.2%±1.1%),both samples exhibited better strength-ductility synergy at room temperature and much higher thermal stabilities at high temperatures(600-700℃)than all those conventional hot-work die steels,which makes the new ODS steel highly promising for advanced hot-work mold and die applications at high temperatures above 600℃.展开更多
It is urgent to develop high-performance polyimide(PI)films that simultaneously exhibit high transparency,exceptional thermal stability,mechanical robustness,and low dielectric to fulfil the requirements of flexible d...It is urgent to develop high-performance polyimide(PI)films that simultaneously exhibit high transparency,exceptional thermal stability,mechanical robustness,and low dielectric to fulfil the requirements of flexible display technologies.Herein,a series of fluorinated polyimide films(FPIs)were fabricated by the condensation of 5,5′-(perfluoropropane-2,2-diyl)bis(isobenzofuran-1,3-dione)(6FDA)and the fluorinated triphenylmethane diamine monomer(EDA,MEDA and DMEDA)with heat-crosslinkable tetrafluorostyrene side groups,which was incorporated by different numbers of methyl groups pendant in the ortho position of amino groups.Subsequently,the FPI films underwent heating to produce crosslinking FPIs(C-FPIs)through the self-crosslinking of double bonds in the tetrafluorostyrene.The transparency,solvent resistance,thermal stability,mechanical robustness and dielectric properties of FPI and C-FPI films can be tuned by the number of methyl groups and crosslinking,which were deeply investigated by virtue of molecular dynamics(MD)simulations and density functional theory(DFT).As a result,all the films exhibited exceptional optically colorless and transparent,with transmittance in the visible region of 450-700 nm exceeding 79.9%,and the cut-off wavelengths(λ_(off))were nearly 350 nm.The thermal decomposition temperatures at 5% weight loss(T_(d5%))for all samples exceeded 504℃.These films exhibited a wide range of tunable tensile strength(46.5-75.1 MPa).Significantly,they showed exceptional dielectric properties with the dielectric constant of 2.3-2.5 at full frequency(10^(7)-20 Hz).This study not only highlights the relationship between the polymer molecular structure and properties,but offer insights for balancing optical transparency,heat resistance and low dielectric constant in PI films.展开更多
Low energy-storage density and inferior thermal stability are a long-term obstacle to the advancement of pulse power devices.Herein,these concerns are addressed by improving bandgap and fabricating polar nanoregions,a...Low energy-storage density and inferior thermal stability are a long-term obstacle to the advancement of pulse power devices.Herein,these concerns are addressed by improving bandgap and fabricating polar nanoregions,and the superior high efficiency of~86.7%,excellent thermal stability of~2%(31-160℃)and energy density of~6.8 J·cm^(-3)are achieved in Bi_(0.5)Na_(0.5)TiO_(3)-La_(0.1)Sr_(0.8)TiO_(3)-δ-NaNbO_(3)ceramics.The high breakdown strength(460 kV·cm^(-1))is ascribed to the broadened bandgap and refined grain.Slim ferroelectric loops originate from the construction of polar nanoregions(PNRs)in a pseudocubic matrix,and transmission electron microscope and piezoelectric force microscope measurements reveal the occurrence of PNRs.The phase-field stimulation and UV-Vis spectrophotometer measurement reveal that the increased grain boundary density and bandgap are beneficial for promoting breakdown strength.The strategy provides an efficient path to prepare Bi_(0.5)Na_(0.5)TiO_(3)La_(0.1)Sr_(0.8)TiO_(3)-δ-based ceramics with superior efficiency,high energy density and outstanding thermal stability.展开更多
High-efficient rubber antioxidants for enhanced heat resistance without compromising mechanical properties remain an enormous and long-term challenge for the rubber industry.Herein,we employed the in-situ growth of Ce...High-efficient rubber antioxidants for enhanced heat resistance without compromising mechanical properties remain an enormous and long-term challenge for the rubber industry.Herein,we employed the in-situ growth of Ce-doped Co-metal-organic framework(Ce Co-MOF)in dendritic mesoporous organosilica nanoparticles(DMONs@Ce Co-MOF,denoted as DCCM)to prepare a novel antioxidant that exhibit outstanding thermal stability.Dendritic mesoporous organosilica nanoparticles(DMONs)effectively alleviated the incompatibility of Ce Co-MOF in the polymer matrix,and the effective scavenging of free radicals was attributed to the various oxidation states of metal ions in Ce Co-MOF.Surprising,by adding only0.5 phr(parts per hundred of rubber)of DMONs@Ce Co-MOF to silicone rubber,(SR),the retention rate of tensile strength increased from 37.3%to 61.6%after aging 72 h at 250℃,and the retention rate of elongation at break of DCCM/SR1 composites reached 68%,which was 5.43 times of SR.The strategy of anchoring MOFs on the surface of silica also provides a viable method for preparing effective compound functionalized rubber antioxidant.展开更多
Achieving high thermal stability in the 6xxx series alloys remains a challenging task,which limits their engineering application.Herein,Al-Mg-Si-Cu alloys with various Mg/Si ratios(0.5,1,2,and 4)were fab-ricated by tw...Achieving high thermal stability in the 6xxx series alloys remains a challenging task,which limits their engineering application.Herein,Al-Mg-Si-Cu alloys with various Mg/Si ratios(0.5,1,2,and 4)were fab-ricated by twin-roll casting(TRC),and the microstructure evolution and mechanical properties during long-term thermal exposure of 150℃/1000 h were studied.The results disclosed that alloys with a high Mg/Si ratio exhibited better thermal stability.The alloys with the Mg/Si ratio of 2(Mg/Si∼2)achieved a stable high yield strength of∼330 MPa and meanwhile maintained a satisfactory fracture elongation(>10%)throughout the thermal exposure process.This excellent thermal stability can be attributed to the microstructure consisting of high-density L phases and fineα-AlFeSi phases,which was related to the optimized Mg/Si ratio.Specifically,L phases were dominated in peak-aged Mg/Si∼2 alloys,while the counterparts in alloys with the Mg/Si ratio of 1(Mg/Si∼1)wereβ’’and Q’phases.During the thermal exposure process,the L phases remained stable without coarsening,which was mainly due to the high coherence and low interfacial energy of the L-matrix interface.Meanwhile,the main Fe-containing phases in Mg/Si∼2 and Mg/Si∼1 alloys were fine near-spheroidalα-AlFeSi and large-size needle-likeβ-AlFeSi,re-spectively,which lead to a better ductility of Mg/Si∼2 alloys.This work may provide a strategy for the preparation of 6xxx series alloys with high thermal stability.展开更多
Nowadays,high-quality phosphor-converted white light-emitting diodes(pc-WLEDs)ought to include cyan-emitting phosphors allowing for full-spectrum light similar to sunlight.Herein,we report a garnetstructured Ce^(3+)-d...Nowadays,high-quality phosphor-converted white light-emitting diodes(pc-WLEDs)ought to include cyan-emitting phosphors allowing for full-spectrum light similar to sunlight.Herein,we report a garnetstructured Ce^(3+)-doped SrLu_(2)Ga_(1.5)Al_(2.5)SiO_(12)(SLGASO)phosphor that significantly compensates for the absence of cyan light,known as the"cyan cavity".The SLGASO host crystallizes into a cubic structure with the Ia3d space group.The cell parameters were determined using Rietveld refinement.Under430 nm blue excitation,SLGASO:Ce^(3+)emits intense cyan-green light in the 450-700 nm wavelength range.The representative SLGASO:0.07Ce^(3+)phosphor has an internal quantum efficiency(IQE)of 95.4%and excellent thermal stability,remaining 92.7%of its initial emission intensity at 152℃.After 155 d of immersion in water,the luminous intensity of SLGASO:0.07Ce^(3+)remains constant,confirming its waterproofness.Furthermore,a pc-WLED device with luminous efficiency(LE)of 101.58 lm/W,color rendering index(Ra)of 91,correlated color temperature(CCT)of 4536 K,and Commission Internationale de L'Eclairage(CIE)chromaticity coordinates of(0.3555,0.3390)was fabricated by combining asprepared cyan-green-emitting SLGASO:0.07Ce^(3+),yellow-emitting Y_(3)Al_(5)O_(12):Ce^(3+)(YAG:Ce^(3+)),and redemitting(Ca,Sr)AlSiN_(3):Eu^(2+)phosphors,as well as a 450 nm blue chip.These findings indicate that SLGASO:0.07Ce^(3+)phosphor can bridge the cyan gap and improve the performance of as-fabricated fullvisible-spectrum WLEDs.展开更多
Dye-based color films are increasingly considered as viable alternatives to pigment-based color films in complementary metal-oxide-semiconductor(CMOS) image sensors.Herein,a series of azo dyes utilizing 5-methyl-2-phe...Dye-based color films are increasingly considered as viable alternatives to pigment-based color films in complementary metal-oxide-semiconductor(CMOS) image sensors.Herein,a series of azo dyes utilizing 5-methyl-2-phenyl-4-(2-phenylhydrazono)-2,4-dihydro-3H-pyrazol-3-one as the coupling component and aromatic amines with various electron-withdrawing groups(NO_(2),CN,Br) as diazo components were designed and synthesized.The presence of intermolecular hydrogen bonding between the hydrogen atom on the N-H group and the oxygen atom of the C=O group of the hydrazo structure facilitates the formation of a stable six-membered ring.Additionally,the electron-withdrawing groups in the diazo component further stabilize this hydrogen-bonded structure.As a result,these azo dyes(P-2,P-3,P-4,P-5)exhibit not only excellent light stability but also ultra-highly thermal stability(T_(d)> 260℃).Therein,the synthesized dyes P-2 and P-3 with great bright yellow color(~400 nm),proper solubility(~6.00g/100 g)were selected to make for color films.And their dye-based color films displayed ultra-highly thermal and light stability(color difference ΔE<3).Notably,the increased planarity of the molecular structure by hydrogen bonding for the novel dyes ensures a balance between high transmittance(>90%) in the 550-780 nm wavelength range and the solvent resistance of the dye-based color films.This work contributes to the advancement of next-generation smart CMOS devices and offers valuable insights into the design of azo dyes for applications in the field of organic electronics.展开更多
The simultaneous integration of high energy density,low sensitivity,and thermal stability in energetic materials has constituted a century-long scientific challenge.Herein,we address this through a dualzwitterionic el...The simultaneous integration of high energy density,low sensitivity,and thermal stability in energetic materials has constituted a century-long scientific challenge.Herein,we address this through a dualzwitterionic electronic delocalization strategy,yielding TYX-3,the first bis-inner salt triazolo-tetrazine framework combining these mutually exclusive properties.Uniformπ-electron distribution and elevated bond dissociation energy confer exceptional thermal stability(T_(d)=365℃)with TATB-level insensitivity(impact sensitivity IS>40 J,friction sensitivity FS>360 N).Engineeredπ-stacked networks enable record density(1.99 g·cm^(-3))with detonation performance surpassing HMX benchmarks(detonation velocity 9315 m·s^(-1),detonation pressure 36.6 GPa).Practical implementation in Poly(3-nitratomethyl-3-methyloxetane)(PNMMFO)solid propellants demonstrates 5.4-fold safety enhancement over conventional HMX-based formulations while maintaining equivalent specific impulse.This work establishes a new design paradigm for energetic materials,overcoming the historical trade-offs between molecular stability and energy output through rational zwitterionic engineering.展开更多
Micrometer-sized,irregularly shaped Ti particles(0.5wt%and 1.0wt%)were mixed with an Al-Si-Mg-Zr matrix powder,and a novel Ti-modified Al-Si-Mg-Zr aluminum alloy was subsequently fabricated via laser-powder bed fusion...Micrometer-sized,irregularly shaped Ti particles(0.5wt%and 1.0wt%)were mixed with an Al-Si-Mg-Zr matrix powder,and a novel Ti-modified Al-Si-Mg-Zr aluminum alloy was subsequently fabricated via laser-powder bed fusion(L-PBF).The results demonstrated that the introduction of Ti particles promoted the formation of near-fully equiaxed grains in the alloy owing to the strong grain refinement of the primary(Al,Si)3(Ti,Zr)nanoparticles.Furthermore,the presence of(Al,Si)3(Ti,Zr)nanoparticles inhibited the decomposition of Si-rich cell boundaries and the precipitation of Si nanoparticles in theα-Al cells.The ultimate tensile strength(UTS),yield strength(YS),and elongation of the asbuilt 0.5wt%Ti(0.5Ti)alloy were(468±11),(350±1)MPa,and(10.0±1.4)%,respectively,which are comparable to those of the L-PBF Al-Si-Mg-Zr matrix alloy and significantly higher than those of traditional L-PBF Al-Si-Mg alloys.After direct aging treatment at 150°C,the precipitation of secondary nanoparticles notably enhanced the strength of the 0.5Ti alloy.Specifically,the 0.5Ti alloy achieved a maximum UTS of(479±11)MPa and YS of(376±10)MPa.At 250°C,the YS of the L-PBF Ti/Al-Si-Mg-Zr alloy was higher than that of the L-PBF Al-Si-Mg-Zr matrix alloy due to the retention of Si-rich cell boundaries,indicating a higher thermal stability.As the aging temperature was increased to 300°C,the dissolution of Si-rich cell boundaries,desolvation of solid-solution elements,and coarsening of nanoprecipitates led to a decrease in the UTS and YS of the alloy to below 300 and 200 MPa,respectively.However,the elongation increased significantly.展开更多
Commercial N52 sintered NdFeB magnets were processed by grain boundary diffusion(GBD)with Dy-Co-M(M=Cu,AI)alloys.The coercivity of magnets greatly increase to 17.62 and 18.83 kOe respectively when diffusing Dy_(58)Co_...Commercial N52 sintered NdFeB magnets were processed by grain boundary diffusion(GBD)with Dy-Co-M(M=Cu,AI)alloys.The coercivity of magnets greatly increase to 17.62 and 18.83 kOe respectively when diffusing Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)alloys,which are obviously higher than that of Dy58Co42GBD-treated magnet with 16.64 kOe,Further thermal stability studies indicate that the thermal stability of Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)GBD-treated magnets is further improved compared to the Dy58Co42GBD-treated magnet The results show that th e temperature coefficients of remanence(20-120℃)are reduced from-0.148%/℃to-0.134%/℃and-0.132%/℃by Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)GBD-treatment,respectively.Besides,the irreversible magnetic flux losses(120℃)for Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)diffusion magnets are 4.76%and 2.79%,respectively.Microstructural analyses demonstrate that the presence of Cu and Al elements reduces the excessive accumulation of Dy and Co on the surface in the diffusion magnets an d improves the diffusion depth and utilization of Dy and Co.Furthermore,the flow of Co from the triple junction phase to the thin grain boundary phase is promoted,which contributes to the uniform distribution of Co.In addition,the dynamic evolution of the magnetic domain structure during the temperature rise process was studied.This work provides insight into the preparation of high-performance and high-thermal stability magnets.展开更多
The thermal stability of lithium-ion battery separators is a critical determinant of battery safety and performance,especially in the context of rapidly expanding applications in electric vehicles and energy storage s...The thermal stability of lithium-ion battery separators is a critical determinant of battery safety and performance,especially in the context of rapidly expanding applications in electric vehicles and energy storage systems.While traditional polyolefin separators(PP/PE)dominate the market due to their cost-effectiveness and mechanical robustness,their inherent poor thermal stability poses significant safety risks under high-temperature conditions.This review provides a comprehensive analysis of recent advancements in enhancing separator thermal stability through coating materials(metal,ceramic,inorganic)and novel high-temperature-resistant polymers(e.g.,PVDF copolymers,PI,PAN).Notably,we critically evaluate the trade-offs between thermal resilience and electrochemical performance,such as the unintended increase in electronic conductivity from metal coatings(e.g.,Cu,MOFs)and reduced electrolyte wettability in ceramic coatings(e.g.,Al_(2)O_(3)).Innovations in hybrid coatings(e.g.,BN/PAN composites,gradient-structured MOFs)and scalable manufacturing techniques(e.g.,roll-to-roll electrospinning)are highlighted as promising strategies to balance these competing demands.Furthermore,a comparative analysis of next-generation high-temperature-resistant separators underscores their ionic conductivity,mechanical strength,and scalability,offering actionable insights for material selection.The review concludes with forward-looking perspectives on integrating machine learning for material discovery,optimizing interfacial adhesion in ceramic coatings,and advancing semi-/all-solid-state batteries to address both thermal and electrochemical challenges.This work aims to bridge the gap between laboratory innovations and industrial applications,fostering safer and more efficient lithium battery technologies.展开更多
Metal nanoparticle(NP_S)catalysts exhibit desirable activities in various catalytic reactions.However,the sintering of metal NPs at high-temperatures even in reducing atmospheres limits its practical application.In th...Metal nanoparticle(NP_S)catalysts exhibit desirable activities in various catalytic reactions.However,the sintering of metal NPs at high-temperatures even in reducing atmospheres limits its practical application.In this work,we successfully synthesized TPA-ZSM-5 with pit-type defects by treating the ZSM-5 with tetrahydroxy ammonium hydroxide(TPAOH),which was then used as a support to prepare Ag-based and Cu-based catalysts.Stability testing results show that the Ag/TPA-ZSM-5 catalyst treated at 800℃with H_(2) could maintain the high performance in NH_(3)-SCO and the Cu/TPA-ZSM-5 catalyst treated at 900℃ with N_(2) could maintained its excellent activity in NH_(3)-SCR,however,the activities of Ag/ZSM-5 and Cu/ZSM-5 were drastically decreased or even deactivated after high-temperature treatment.In addition,a series of characterization analyses revealed that the excellent thermal stability is attribute to the presence of pit-type defects in the TPA-ZSM-5 as physical barriers to slow down or even inhibit the Ag NPs and Cu NPs sintering process.The strategy of using the pit-type defects to inhibit the sintering of metal NPs and improve the thermal stability can greatly enhance the practical application of catalysts.展开更多
Sintered metals serving as thermal interface materials(TIMs)with superior thermal conductivities show the most promise in meeting the heat dissipation requirements of next-generation wide bandgap applications.Neverthe...Sintered metals serving as thermal interface materials(TIMs)with superior thermal conductivities show the most promise in meeting the heat dissipation requirements of next-generation wide bandgap applications.Nevertheless,their thermal stabilities during high-temperature service provide significant challenges.Herein,a facile approach was developed for one-step synthesis of single-phase Ag-Cu supersaturated solid-solution nanoparticle(Ag-Cu SS-NP)pastes with adjustable Cu contents(up to 37.7 at.%),and they exhibited ultrahigh resistance to oxidation and excellent sinterability.A paste composed of Ag-Cu SS-NPs was sintered in air at 250℃ for 20 min,and this resulted in a dense supersaturated structure with an impressive thermal conductivity of 157.8 W/(m K)and a room-temperature shear strength of 133.4 MPa.Microstructural analyses demonstrated that Cu had precipitated from the Ag lattice to form Cu nanoprecipitates,which refined the grain sizes and induced high-density dislocations during sintering.For the pinning effect of dislocations and grain boundaries by the Cu nanoprecipitates and coherent twins,the high-temperature(400℃)shear strength of sintered Ag-Cu SS-NP joints was significantly improved by 67%(58.6 MPa),meanwhile the shear strength after long-term aging at 200 and 300℃for 960 h were increased by 123%(140.3 MPa)and 80%(82.4 MPa)compared to those of sintered Ag NP joints,respectively.The remarkable thermal stability is far superior to traditional TIMs,so the Ag-Cu SS-NP paste exhibits excellent potential as a TIM for high-temperature power device applications.展开更多
The rapid expansion of the automotive sector has significantly increased the demand for highperformance lithium-ion batteries,positioning Ni-rich layered cathodes as a promising solution due to their high energy densi...The rapid expansion of the automotive sector has significantly increased the demand for highperformance lithium-ion batteries,positioning Ni-rich layered cathodes as a promising solution due to their high energy density and cost-efficiency.However,these cathodes face critical challenges,including thermal instability and structural degradation at an elevated temperature,which hinder their practical application.This study introduces an advanced surface reconstruction strategy combining a LiScF_(4)coating,Sc/F surface co-doping,and a cation-mixing layer to address these issues.The LiScF_(4)coating serves as a durable protective barrier,reducing electrolyte decomposition,minimizing transition metal dissolution,and enhancing lithium-ion transport.Sc/F surface co-doping stabilizes lattice oxygen by increasing the energy barrier for oxygen vacancy formation and minimizing oxygen release,thereby suppressing phase transitions and interfacial side reactions.Additionally,the cation-mixing layer improves interfacial stability by alleviating lattice strain and supporting reversible cation migration,ensuring prolonged durability during cycling and under high-temperature conditions.These integrated modifications work synergistically to mitigate various degradation mechanisms,significantly improving the thermal stability,structural integrity,and electrochemical performance of Ni-rich cathodes.This approach offers a viable pathway for incorporating Ni-rich cathodes into advanced lithium-ion batteries,making them well-suited for applications requiring high thermal stability.Moreover,this research provides valuable guidance for the development of a multi-component modification strategy,paving the way for future innovations in energy storage materials and advancing high-performance battery technology.展开更多
Nanocrystalline alloys often exhibit unusual thermal stability as a consequence of kinetic and thermodynamic barriers to grain growth.However,the physical mechanisms governing alloy stability need to be identified.In ...Nanocrystalline alloys often exhibit unusual thermal stability as a consequence of kinetic and thermodynamic barriers to grain growth.However,the physical mechanisms governing alloy stability need to be identified.In this work,we found that grain boundary(GB)relaxation renders Ni-W alloyed films relatively stable at low annealing temperature,while twinning-mediated grain growth occurs via dislocation-GB/twin boundary(TB)interactions as the annealing temperature increases.At a relatively low temperature,TB strengthening plays a dominant role in plastic deformation,whereas precipitation strengthening gradually controls the deformation mechanism with the increase of annealing temperature.Our findings provide evidence for improving mechanical property through alloying and microstructure design,and have a crucial guiding significance in material selection and miniaturized applications such as Micro Electro Mechanical Systems.展开更多
A novel Eu^(3+)-doped fluorapatite red phosphor Ca_(2)Y_(8)(BO_(4))_(2)(SiO_(4))_(4)F_(2)Eu^(3+)with pure phase was synthesized in this study.Density functional theory(DFT)calculation and diffuse reflection spectrum a...A novel Eu^(3+)-doped fluorapatite red phosphor Ca_(2)Y_(8)(BO_(4))_(2)(SiO_(4))_(4)F_(2)Eu^(3+)with pure phase was synthesized in this study.Density functional theory(DFT)calculation and diffuse reflection spectrum analysis reveal its potential as a matrix for phosphors excited by ultraviolet light.Eu^(3+)has a^(7)F_(0)→^(5)L_(6)transition at 394 nm,and the prepared phosphor exhibits a high emission intensity at 614 nm,which may be attributed to the^(5)D_(0)-^(7)F_(2)energy transition at the lower symmetry site of Eu^(3+).The optimal doping concentration of the phosphor is determined to be 11 mol%,with concentration quenching attributed to the exchange interaction mechanism.The overall color purity of the phosphor is up to 99.88%,with an internal quantum efficiency as high as 91.15%.Notably,Ca_(2)Y_(8)(BO_(4))_(2)(SiO_(4))_(4)F_(2):11 mol%Eu^(3+)(CYBSF:11 mol%Eu^(3+))phosphors exhibit good thermal stability,with a thermal quenching temperature(T1/2)of 552 K and the intensity of emission at 423 K still at 88.89%of that at 298 K.The activation energy of the phosphor is up to 0.30287 eV.Its comprehensive luminescence performance surpasses that of commercial red phosphor,making it suitable for near ultraviolet excited warm white light emitting diode(NUV-WLED)with a high color rendering index(Ra=82)and a correlated color temperature(CCT)of 4339 K.Moreover,the phosphor achieves latent fingerprint visualization and anti-counterfeiting ink on different material surfaces:glass,aluminum foil,plastic and paper.Overall,the fluorapatite CYBSF:11 mol%Eu^(3+)phosphor holds great potential for multimodal applications due to its high quantum efficiency and good thermal stability.展开更多
The substitution of Fe by Co in the 2:14:1 phase is an effective method to increase the Curie temperature and enhance the thermal stability of the Nd-Fe-B magnets.However,the accumulation of Co ele ment at the grain b...The substitution of Fe by Co in the 2:14:1 phase is an effective method to increase the Curie temperature and enhance the thermal stability of the Nd-Fe-B magnets.However,the accumulation of Co ele ment at the grain boundaries(GBs) changes the GBs from nonmagnetic to ferromagnetic and causes the thinlayer GBs to become rare,In this paper,the method of diffusing Tb element was chosen to improve the microstructure and temperature stability of high-Co magnets.Three original sintered Nd_(28.5)Dy_(3)-CO_(x)e_(bal)M_(0.6)B_(i)(x=0,6 wt%,12 wt%;M = Cu,Al,Zr) magnets with different Co contents were diffused with Tb by grain boundary diffusion(GBD).After GBD,high-Co magnets exhibit more continuously distributed thin-layer GBs,and their thermal stability is significantly improved.In high-Co magnets(x=6 wt%),the absolute value of the temperature coefficient of coercivity decreases from 0.603%/K to0.508%/K in the temperature range of 293-413 K,that of remanence decreases from 0.099%/K to 0.091%/K,and the coercivity increases from 18.44 to 25.04 kOe.Transmission electron microscopy(TEM)characterization reveals that there are both the 1:2 phase and the amorphous phase in the high-Co magnet before and after GBD,EDS elemental analysis shows that Tb element is more likely to preferentially replace the rare earth elements in the 2:14:1 main phase than in the 1:2 phase and the amorphous phase.The concentration of Tb at the edge of the main phase is much higher than that in the 1:2phase and amorphous phase,which is beneficial to the improvement of the microstructure.The preferential replacement of Tb elements at the edge of the 2:14:1 phase and thin-layer GBs with a more continuous distribution are synergistically responsible for improving the thermal stability of high-Co magnets.The study indicates that GBD is an effective method to improve the microstructure and thermal stability of high-Co magnets.展开更多
This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The...This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The addition of non-halogen flame retardants(FRs)including aluminum trihydroxide(ATH),triphenyl phosphate(TPP),and diammonium phosphate(DAP)leads to markedly enhanced thermal sta-bility and fire resistance of the PU/nSiO_(2)/FRs nanocomposites,resulting in achieving UL-94 HB standard.In particular,the nanocomposites met the UL-94 V-0 criteria thanks to the inclusion of DAP at 25 phr.The LOI value of the nanocomposites reached 26%which is much higher than that of PU/nSiO_(2)nanocompos-ite,about 20%.In order to further understand the fire-proof mechanism,the residue char layer remaining of the PU/nSiO_(2)/FRs nanocomposites after being burned was also investigated by scanning electron mi-croscopy(SEM)and Fourier transform infrared(FTIR).In addition,the microstructure,thermal stability,thermal conductivity,and mechanical properties of nanocomposites were also evaluated in this study.展开更多
基金supported by the National Natural Science Foundation of China(52404259)supported by Youth Innovation Promotion Association CAS(Y201768)。
文摘The future large-scale application of sodium-ion batteries(SIBs)is inseparable from their excellent electrochemical performance and reliable safety characteristics.At present,there are few studies focusing on their safety performance.The analysis of thermal stability and structural changes within a single material cannot systematically describe the complex interplay of components within the battery system during the thermal runaway process.Furthermore,the reaction between the battery materials themselves and their counterparts within the system can stimulate more intense exothermic behavior,thereby affecting the safety of the entire battery system.Therefore,this study delved into the thermal generation and gas evolution characteristics of the positive electrode(Na_(x)Ni_(1/3)Fe_(1/3)Mn_(1/3)O_(2),NFM111)and the negative electrode(hard carbon,HC)in SIBs,utilizing various material combinations.Through the integration of microscopic and macroscopic characterization techniques,the underlying reaction mechanisms of the positive and negative electrode materials within the battery during the heating process were elucidated.Three important results are derived from this study:(Ⅰ)The instability of the solid electrolyte interphase(SEI)leads to its decomposition at temperatures below 100℃,followed by extensive decomposition within the range of 100-150℃,yielding heat and the formation of inorganic compounds,such as Na_(2)CO_(3)and Na_(2)O;(Ⅱ)The reaction between NFM111 and the electrolyte constitutes the primary exothermic event during thermal abuse,with a discernible reaction also occurring between sodium metal and the electrolyte throughout the heating process;(Ⅲ)The heat production and gas generation behaviors of multi-component reactions do not exhibit complete correlation,and the occurrence of gas production does not necessarily coincide with thermal behavior.The results presented in this study can provide useful guidance for the safety improvement of SIBs.
文摘Thermal quenching(TQ)at elevated temperature is a major factor affecting the luminescent intensity and efficiency of phosphors.Improving the thermal stability of phosphors and weakening the TQ effect are of significance for the high-quality illumination of phosphor-converted WLEDs.Here,a novel red-emitting phosphor K_(2)Zn(PO_(3))_(4)∶Mn^(2+)is synthesized by standard high temperature solid state reaction in ambient atmosphere,which is a new member of self-reduction system.An effective synthesis strategy is proposed to optimize its photoluminescent performances.Combined with X-ray photoelectron spectroscopy and X-ray absorption fine structure spectroscopy,oxygen vacancy defects introduced by Mn doping are proved to play an important role in the transition of Mn^(4+)→Mn^(2+).Thermoluminescence analysis reveals that the distribution of trap levels,especially the deep ones,is effectively regulated by the controllable crystallization and significantly affect the thermal stability of phosphors.Then a defect-assisted model is proposed to address the inner mechanism of the phenomenon.The carriers trapped by deep trap levels can be released under the high-temperature stimulus,which return back to the luminescent centers and participate in the radiative recombination to improve thermal stability.This study provides a new crystallographic idea and theoretical support for obtaining luminescent materials with high thermal stability.
基金support from the National MCF Energy R&D Program of China(No.2018YFE0306100).
文摘A novel oxide-dispersion-strengthened(ODS)die steel was fabricated by mechanical alloying and hot consolidation.Annealing and quench-tempering treatments both obtained an ultra-fine grain structure(mean size:310-330 nm)with an ultra-high density of ultra-fine Y-Al-O nano-oxides(number density:~(1-1.5)×10^(23)m^(−3),mean size:5.1-7.2 nm).Prolonged thermal exposure further induced the new,highly dense precipitation of ultra-fine Y-Zr-O nano-oxides.Both nano-oxides tended to be wrapped up with a B2-NiAl nano-shells.Although the quench-tempered sample showed much higher room-temperature strength(yield strength=1393±40 MPa and ultimate tensile strength=1774±11 MPa)and slightly lower elongation(elongation=13.6%±0.6%)than the annealed sample(YS=988±7 MPa,UTS=1490±12 MPa,and EL=15.2%±1.1%),both samples exhibited better strength-ductility synergy at room temperature and much higher thermal stabilities at high temperatures(600-700℃)than all those conventional hot-work die steels,which makes the new ODS steel highly promising for advanced hot-work mold and die applications at high temperatures above 600℃.
基金financially supported by the Natural Science Foundation of Shandong Province(Nos.ZR2021ME055,ZR2022QB170 and ZR2022MB034)the Foundation(No.GZKF202128)of State Key Laboratory of Biobased Material and Green Papermaking,Qilu University of Technology,Shandong Academy of Sciencesthe Development Program Project of Young Innovation Team of Institutions of Higher Learning in Shandong Province.
文摘It is urgent to develop high-performance polyimide(PI)films that simultaneously exhibit high transparency,exceptional thermal stability,mechanical robustness,and low dielectric to fulfil the requirements of flexible display technologies.Herein,a series of fluorinated polyimide films(FPIs)were fabricated by the condensation of 5,5′-(perfluoropropane-2,2-diyl)bis(isobenzofuran-1,3-dione)(6FDA)and the fluorinated triphenylmethane diamine monomer(EDA,MEDA and DMEDA)with heat-crosslinkable tetrafluorostyrene side groups,which was incorporated by different numbers of methyl groups pendant in the ortho position of amino groups.Subsequently,the FPI films underwent heating to produce crosslinking FPIs(C-FPIs)through the self-crosslinking of double bonds in the tetrafluorostyrene.The transparency,solvent resistance,thermal stability,mechanical robustness and dielectric properties of FPI and C-FPI films can be tuned by the number of methyl groups and crosslinking,which were deeply investigated by virtue of molecular dynamics(MD)simulations and density functional theory(DFT).As a result,all the films exhibited exceptional optically colorless and transparent,with transmittance in the visible region of 450-700 nm exceeding 79.9%,and the cut-off wavelengths(λ_(off))were nearly 350 nm.The thermal decomposition temperatures at 5% weight loss(T_(d5%))for all samples exceeded 504℃.These films exhibited a wide range of tunable tensile strength(46.5-75.1 MPa).Significantly,they showed exceptional dielectric properties with the dielectric constant of 2.3-2.5 at full frequency(10^(7)-20 Hz).This study not only highlights the relationship between the polymer molecular structure and properties,but offer insights for balancing optical transparency,heat resistance and low dielectric constant in PI films.
基金supported by the National Natural Science Foundation of China(Nos.12364015 and 52176072)the Five-Year Action Plan for Shccig-Qinling Program and Key Project of Hubei Province Key Research and Development Plan(No.2021BCA140)+4 种基金the Industry and Education Combination Innovation Platform of Intelligent Manufacturing and Graduate Joint Training Base at Guizhou University(No.2020-520000-83-01-324061)the National Key Research and Development Plan(No.2022YFF0706500)Guizhou University Natural Science Special(special post)Research Fund(No.(2023)17)Guizhou Engineering Research Center for Smart Services(No.2203-520102-04-04-298868)the Construction of Science and Technology Platform of Guiyang(No.[2023]7-3).
文摘Low energy-storage density and inferior thermal stability are a long-term obstacle to the advancement of pulse power devices.Herein,these concerns are addressed by improving bandgap and fabricating polar nanoregions,and the superior high efficiency of~86.7%,excellent thermal stability of~2%(31-160℃)and energy density of~6.8 J·cm^(-3)are achieved in Bi_(0.5)Na_(0.5)TiO_(3)-La_(0.1)Sr_(0.8)TiO_(3)-δ-NaNbO_(3)ceramics.The high breakdown strength(460 kV·cm^(-1))is ascribed to the broadened bandgap and refined grain.Slim ferroelectric loops originate from the construction of polar nanoregions(PNRs)in a pseudocubic matrix,and transmission electron microscope and piezoelectric force microscope measurements reveal the occurrence of PNRs.The phase-field stimulation and UV-Vis spectrophotometer measurement reveal that the increased grain boundary density and bandgap are beneficial for promoting breakdown strength.The strategy provides an efficient path to prepare Bi_(0.5)Na_(0.5)TiO_(3)La_(0.1)Sr_(0.8)TiO_(3)-δ-based ceramics with superior efficiency,high energy density and outstanding thermal stability.
基金support from the Beijing Natural Science Foundation(No.JQ23035)。
文摘High-efficient rubber antioxidants for enhanced heat resistance without compromising mechanical properties remain an enormous and long-term challenge for the rubber industry.Herein,we employed the in-situ growth of Ce-doped Co-metal-organic framework(Ce Co-MOF)in dendritic mesoporous organosilica nanoparticles(DMONs@Ce Co-MOF,denoted as DCCM)to prepare a novel antioxidant that exhibit outstanding thermal stability.Dendritic mesoporous organosilica nanoparticles(DMONs)effectively alleviated the incompatibility of Ce Co-MOF in the polymer matrix,and the effective scavenging of free radicals was attributed to the various oxidation states of metal ions in Ce Co-MOF.Surprising,by adding only0.5 phr(parts per hundred of rubber)of DMONs@Ce Co-MOF to silicone rubber,(SR),the retention rate of tensile strength increased from 37.3%to 61.6%after aging 72 h at 250℃,and the retention rate of elongation at break of DCCM/SR1 composites reached 68%,which was 5.43 times of SR.The strategy of anchoring MOFs on the surface of silica also provides a viable method for preparing effective compound functionalized rubber antioxidant.
基金Financial supports are from the National Natural Science Foun-dation of China(Nos.52261015 and U22A20109)the Inner Mongolia Natural Science Foundation(No.2022QN05005)+2 种基金the Basic Scientific Research Expenses Program of Universities directly under Inner Mongolia Autonomous Region(No.JY20220109)the Scientific Research Project of Inner Mongolia University of Technology(No.ZZ202104)the Science Research Project of Hebei Education Department(No.BJK2024023 and BJK2024061).
文摘Achieving high thermal stability in the 6xxx series alloys remains a challenging task,which limits their engineering application.Herein,Al-Mg-Si-Cu alloys with various Mg/Si ratios(0.5,1,2,and 4)were fab-ricated by twin-roll casting(TRC),and the microstructure evolution and mechanical properties during long-term thermal exposure of 150℃/1000 h were studied.The results disclosed that alloys with a high Mg/Si ratio exhibited better thermal stability.The alloys with the Mg/Si ratio of 2(Mg/Si∼2)achieved a stable high yield strength of∼330 MPa and meanwhile maintained a satisfactory fracture elongation(>10%)throughout the thermal exposure process.This excellent thermal stability can be attributed to the microstructure consisting of high-density L phases and fineα-AlFeSi phases,which was related to the optimized Mg/Si ratio.Specifically,L phases were dominated in peak-aged Mg/Si∼2 alloys,while the counterparts in alloys with the Mg/Si ratio of 1(Mg/Si∼1)wereβ’’and Q’phases.During the thermal exposure process,the L phases remained stable without coarsening,which was mainly due to the high coherence and low interfacial energy of the L-matrix interface.Meanwhile,the main Fe-containing phases in Mg/Si∼2 and Mg/Si∼1 alloys were fine near-spheroidalα-AlFeSi and large-size needle-likeβ-AlFeSi,re-spectively,which lead to a better ductility of Mg/Si∼2 alloys.This work may provide a strategy for the preparation of 6xxx series alloys with high thermal stability.
基金supported by the National Natural Science Foundations of China(21801254,52002411,52272174,22205017,U1301242)China Postdoctoral Science Foundation(2022M720400,2023M743978)+1 种基金Specialized Research Fund for the Doctoral Program of Higher Education of China(20130171130001)the Ministry of Science,Technological Development,and Innovation of the Republic of Serbia(451-03-66/2024-03/200017)。
文摘Nowadays,high-quality phosphor-converted white light-emitting diodes(pc-WLEDs)ought to include cyan-emitting phosphors allowing for full-spectrum light similar to sunlight.Herein,we report a garnetstructured Ce^(3+)-doped SrLu_(2)Ga_(1.5)Al_(2.5)SiO_(12)(SLGASO)phosphor that significantly compensates for the absence of cyan light,known as the"cyan cavity".The SLGASO host crystallizes into a cubic structure with the Ia3d space group.The cell parameters were determined using Rietveld refinement.Under430 nm blue excitation,SLGASO:Ce^(3+)emits intense cyan-green light in the 450-700 nm wavelength range.The representative SLGASO:0.07Ce^(3+)phosphor has an internal quantum efficiency(IQE)of 95.4%and excellent thermal stability,remaining 92.7%of its initial emission intensity at 152℃.After 155 d of immersion in water,the luminous intensity of SLGASO:0.07Ce^(3+)remains constant,confirming its waterproofness.Furthermore,a pc-WLED device with luminous efficiency(LE)of 101.58 lm/W,color rendering index(Ra)of 91,correlated color temperature(CCT)of 4536 K,and Commission Internationale de L'Eclairage(CIE)chromaticity coordinates of(0.3555,0.3390)was fabricated by combining asprepared cyan-green-emitting SLGASO:0.07Ce^(3+),yellow-emitting Y_(3)Al_(5)O_(12):Ce^(3+)(YAG:Ce^(3+)),and redemitting(Ca,Sr)AlSiN_(3):Eu^(2+)phosphors,as well as a 450 nm blue chip.These findings indicate that SLGASO:0.07Ce^(3+)phosphor can bridge the cyan gap and improve the performance of as-fabricated fullvisible-spectrum WLEDs.
基金supported by the Program of the National Natural Science Foundation of China(No.22238002)the Fundamental Research Funds for the Central Universities(No.DUT22LAB610)+1 种基金Research and Innovation Team Project of Dalian University of Technology(No.DUT2022TB10)China Postdoctoral Science Foundation(No.2022M720639)。
文摘Dye-based color films are increasingly considered as viable alternatives to pigment-based color films in complementary metal-oxide-semiconductor(CMOS) image sensors.Herein,a series of azo dyes utilizing 5-methyl-2-phenyl-4-(2-phenylhydrazono)-2,4-dihydro-3H-pyrazol-3-one as the coupling component and aromatic amines with various electron-withdrawing groups(NO_(2),CN,Br) as diazo components were designed and synthesized.The presence of intermolecular hydrogen bonding between the hydrogen atom on the N-H group and the oxygen atom of the C=O group of the hydrazo structure facilitates the formation of a stable six-membered ring.Additionally,the electron-withdrawing groups in the diazo component further stabilize this hydrogen-bonded structure.As a result,these azo dyes(P-2,P-3,P-4,P-5)exhibit not only excellent light stability but also ultra-highly thermal stability(T_(d)> 260℃).Therein,the synthesized dyes P-2 and P-3 with great bright yellow color(~400 nm),proper solubility(~6.00g/100 g)were selected to make for color films.And their dye-based color films displayed ultra-highly thermal and light stability(color difference ΔE<3).Notably,the increased planarity of the molecular structure by hydrogen bonding for the novel dyes ensures a balance between high transmittance(>90%) in the 550-780 nm wavelength range and the solvent resistance of the dye-based color films.This work contributes to the advancement of next-generation smart CMOS devices and offers valuable insights into the design of azo dyes for applications in the field of organic electronics.
基金supported by the National Natural Science Foundation of China(Grant Nos.22105156,22175139,22171136,and 22302156)the China National Science Fund for Distinguished Young Scholars(Grant No.22325504)。
文摘The simultaneous integration of high energy density,low sensitivity,and thermal stability in energetic materials has constituted a century-long scientific challenge.Herein,we address this through a dualzwitterionic electronic delocalization strategy,yielding TYX-3,the first bis-inner salt triazolo-tetrazine framework combining these mutually exclusive properties.Uniformπ-electron distribution and elevated bond dissociation energy confer exceptional thermal stability(T_(d)=365℃)with TATB-level insensitivity(impact sensitivity IS>40 J,friction sensitivity FS>360 N).Engineeredπ-stacked networks enable record density(1.99 g·cm^(-3))with detonation performance surpassing HMX benchmarks(detonation velocity 9315 m·s^(-1),detonation pressure 36.6 GPa).Practical implementation in Poly(3-nitratomethyl-3-methyloxetane)(PNMMFO)solid propellants demonstrates 5.4-fold safety enhancement over conventional HMX-based formulations while maintaining equivalent specific impulse.This work establishes a new design paradigm for energetic materials,overcoming the historical trade-offs between molecular stability and energy output through rational zwitterionic engineering.
基金supported by the National Natural Science Foundation of China(Nos.52001140 and 52475361).
文摘Micrometer-sized,irregularly shaped Ti particles(0.5wt%and 1.0wt%)were mixed with an Al-Si-Mg-Zr matrix powder,and a novel Ti-modified Al-Si-Mg-Zr aluminum alloy was subsequently fabricated via laser-powder bed fusion(L-PBF).The results demonstrated that the introduction of Ti particles promoted the formation of near-fully equiaxed grains in the alloy owing to the strong grain refinement of the primary(Al,Si)3(Ti,Zr)nanoparticles.Furthermore,the presence of(Al,Si)3(Ti,Zr)nanoparticles inhibited the decomposition of Si-rich cell boundaries and the precipitation of Si nanoparticles in theα-Al cells.The ultimate tensile strength(UTS),yield strength(YS),and elongation of the asbuilt 0.5wt%Ti(0.5Ti)alloy were(468±11),(350±1)MPa,and(10.0±1.4)%,respectively,which are comparable to those of the L-PBF Al-Si-Mg-Zr matrix alloy and significantly higher than those of traditional L-PBF Al-Si-Mg alloys.After direct aging treatment at 150°C,the precipitation of secondary nanoparticles notably enhanced the strength of the 0.5Ti alloy.Specifically,the 0.5Ti alloy achieved a maximum UTS of(479±11)MPa and YS of(376±10)MPa.At 250°C,the YS of the L-PBF Ti/Al-Si-Mg-Zr alloy was higher than that of the L-PBF Al-Si-Mg-Zr matrix alloy due to the retention of Si-rich cell boundaries,indicating a higher thermal stability.As the aging temperature was increased to 300°C,the dissolution of Si-rich cell boundaries,desolvation of solid-solution elements,and coarsening of nanoprecipitates led to a decrease in the UTS and YS of the alloy to below 300 and 200 MPa,respectively.However,the elongation increased significantly.
基金Project supported by the National Key R&D Program of China(2022YFB3505003,2021YFB3502802)the Natural Science Foundation of Zhejiang Province(LQ23E010001)+3 种基金"Pioneer"and"Leading Goose"R&D program of Zhejiang(2022C01020)Key Research and Development Program of Ningbo City(2023Z093)Kunpeng Plan of Zhejiang ProvinceNingbo Top Talent Program。
文摘Commercial N52 sintered NdFeB magnets were processed by grain boundary diffusion(GBD)with Dy-Co-M(M=Cu,AI)alloys.The coercivity of magnets greatly increase to 17.62 and 18.83 kOe respectively when diffusing Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)alloys,which are obviously higher than that of Dy58Co42GBD-treated magnet with 16.64 kOe,Further thermal stability studies indicate that the thermal stability of Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)GBD-treated magnets is further improved compared to the Dy58Co42GBD-treated magnet The results show that th e temperature coefficients of remanence(20-120℃)are reduced from-0.148%/℃to-0.134%/℃and-0.132%/℃by Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)GBD-treatment,respectively.Besides,the irreversible magnetic flux losses(120℃)for Dy_(58)Co_(25)Cu_(17)and Dy_(58)Co_(25)Al_(17)diffusion magnets are 4.76%and 2.79%,respectively.Microstructural analyses demonstrate that the presence of Cu and Al elements reduces the excessive accumulation of Dy and Co on the surface in the diffusion magnets an d improves the diffusion depth and utilization of Dy and Co.Furthermore,the flow of Co from the triple junction phase to the thin grain boundary phase is promoted,which contributes to the uniform distribution of Co.In addition,the dynamic evolution of the magnetic domain structure during the temperature rise process was studied.This work provides insight into the preparation of high-performance and high-thermal stability magnets.
基金supported by Beijing Institute of Technology Student Innovation Training Program(BIT2024LH013).
文摘The thermal stability of lithium-ion battery separators is a critical determinant of battery safety and performance,especially in the context of rapidly expanding applications in electric vehicles and energy storage systems.While traditional polyolefin separators(PP/PE)dominate the market due to their cost-effectiveness and mechanical robustness,their inherent poor thermal stability poses significant safety risks under high-temperature conditions.This review provides a comprehensive analysis of recent advancements in enhancing separator thermal stability through coating materials(metal,ceramic,inorganic)and novel high-temperature-resistant polymers(e.g.,PVDF copolymers,PI,PAN).Notably,we critically evaluate the trade-offs between thermal resilience and electrochemical performance,such as the unintended increase in electronic conductivity from metal coatings(e.g.,Cu,MOFs)and reduced electrolyte wettability in ceramic coatings(e.g.,Al_(2)O_(3)).Innovations in hybrid coatings(e.g.,BN/PAN composites,gradient-structured MOFs)and scalable manufacturing techniques(e.g.,roll-to-roll electrospinning)are highlighted as promising strategies to balance these competing demands.Furthermore,a comparative analysis of next-generation high-temperature-resistant separators underscores their ionic conductivity,mechanical strength,and scalability,offering actionable insights for material selection.The review concludes with forward-looking perspectives on integrating machine learning for material discovery,optimizing interfacial adhesion in ceramic coatings,and advancing semi-/all-solid-state batteries to address both thermal and electrochemical challenges.This work aims to bridge the gap between laboratory innovations and industrial applications,fostering safer and more efficient lithium battery technologies.
基金supported by the National Natural Science Foundation of China(No.52370113)Yunnan Fundamental Research Projects(No.202101BE070001-001)。
文摘Metal nanoparticle(NP_S)catalysts exhibit desirable activities in various catalytic reactions.However,the sintering of metal NPs at high-temperatures even in reducing atmospheres limits its practical application.In this work,we successfully synthesized TPA-ZSM-5 with pit-type defects by treating the ZSM-5 with tetrahydroxy ammonium hydroxide(TPAOH),which was then used as a support to prepare Ag-based and Cu-based catalysts.Stability testing results show that the Ag/TPA-ZSM-5 catalyst treated at 800℃with H_(2) could maintain the high performance in NH_(3)-SCO and the Cu/TPA-ZSM-5 catalyst treated at 900℃ with N_(2) could maintained its excellent activity in NH_(3)-SCR,however,the activities of Ag/ZSM-5 and Cu/ZSM-5 were drastically decreased or even deactivated after high-temperature treatment.In addition,a series of characterization analyses revealed that the excellent thermal stability is attribute to the presence of pit-type defects in the TPA-ZSM-5 as physical barriers to slow down or even inhibit the Ag NPs and Cu NPs sintering process.The strategy of using the pit-type defects to inhibit the sintering of metal NPs and improve the thermal stability can greatly enhance the practical application of catalysts.
基金supported by the National Natural Science Foundation of China(Nos.52075125 and 52105331)the Guangdong Basic and Applied Basic Research Foundation(No.2023A1515010591)the Shenzhen Science and Technology Innovation Committee(Nos.JCYJ20210324124203009,JSGG20201102154600003,GXWD20231130103814001,and GXWD20220721182229001).
文摘Sintered metals serving as thermal interface materials(TIMs)with superior thermal conductivities show the most promise in meeting the heat dissipation requirements of next-generation wide bandgap applications.Nevertheless,their thermal stabilities during high-temperature service provide significant challenges.Herein,a facile approach was developed for one-step synthesis of single-phase Ag-Cu supersaturated solid-solution nanoparticle(Ag-Cu SS-NP)pastes with adjustable Cu contents(up to 37.7 at.%),and they exhibited ultrahigh resistance to oxidation and excellent sinterability.A paste composed of Ag-Cu SS-NPs was sintered in air at 250℃ for 20 min,and this resulted in a dense supersaturated structure with an impressive thermal conductivity of 157.8 W/(m K)and a room-temperature shear strength of 133.4 MPa.Microstructural analyses demonstrated that Cu had precipitated from the Ag lattice to form Cu nanoprecipitates,which refined the grain sizes and induced high-density dislocations during sintering.For the pinning effect of dislocations and grain boundaries by the Cu nanoprecipitates and coherent twins,the high-temperature(400℃)shear strength of sintered Ag-Cu SS-NP joints was significantly improved by 67%(58.6 MPa),meanwhile the shear strength after long-term aging at 200 and 300℃for 960 h were increased by 123%(140.3 MPa)and 80%(82.4 MPa)compared to those of sintered Ag NP joints,respectively.The remarkable thermal stability is far superior to traditional TIMs,so the Ag-Cu SS-NP paste exhibits excellent potential as a TIM for high-temperature power device applications.
基金supported by the National Natural Science Foundation of China(22179008)support from the Beijing Nova Program(20230484241)+1 种基金support from the China Postdoctoral Science Foundation(2024M754084)the Postdoctoral Fellowship Program of CPSF(GZB20230931)。
文摘The rapid expansion of the automotive sector has significantly increased the demand for highperformance lithium-ion batteries,positioning Ni-rich layered cathodes as a promising solution due to their high energy density and cost-efficiency.However,these cathodes face critical challenges,including thermal instability and structural degradation at an elevated temperature,which hinder their practical application.This study introduces an advanced surface reconstruction strategy combining a LiScF_(4)coating,Sc/F surface co-doping,and a cation-mixing layer to address these issues.The LiScF_(4)coating serves as a durable protective barrier,reducing electrolyte decomposition,minimizing transition metal dissolution,and enhancing lithium-ion transport.Sc/F surface co-doping stabilizes lattice oxygen by increasing the energy barrier for oxygen vacancy formation and minimizing oxygen release,thereby suppressing phase transitions and interfacial side reactions.Additionally,the cation-mixing layer improves interfacial stability by alleviating lattice strain and supporting reversible cation migration,ensuring prolonged durability during cycling and under high-temperature conditions.These integrated modifications work synergistically to mitigate various degradation mechanisms,significantly improving the thermal stability,structural integrity,and electrochemical performance of Ni-rich cathodes.This approach offers a viable pathway for incorporating Ni-rich cathodes into advanced lithium-ion batteries,making them well-suited for applications requiring high thermal stability.Moreover,this research provides valuable guidance for the development of a multi-component modification strategy,paving the way for future innovations in energy storage materials and advancing high-performance battery technology.
基金supported by the National Natural Science Foundation of China(Grant Nos.92163201,52431006,52441407,U23A6013,92360301 and U2330203)the Shaanxi Province Innovation Team Project(2024RS-CXTD-58)+2 种基金the Shaanxi Province Youth Innovation Team Project(22JP042)the Natural Science Basic Research Plan in Shaanxi Province(2022JQ-460)the Fundamental Research Funds for the Central Universities(xtr062024006,xtr022019004 and xzy022022024).
文摘Nanocrystalline alloys often exhibit unusual thermal stability as a consequence of kinetic and thermodynamic barriers to grain growth.However,the physical mechanisms governing alloy stability need to be identified.In this work,we found that grain boundary(GB)relaxation renders Ni-W alloyed films relatively stable at low annealing temperature,while twinning-mediated grain growth occurs via dislocation-GB/twin boundary(TB)interactions as the annealing temperature increases.At a relatively low temperature,TB strengthening plays a dominant role in plastic deformation,whereas precipitation strengthening gradually controls the deformation mechanism with the increase of annealing temperature.Our findings provide evidence for improving mechanical property through alloying and microstructure design,and have a crucial guiding significance in material selection and miniaturized applications such as Micro Electro Mechanical Systems.
基金supported by the National Natural Science Foundation of China(52372013)Natural Science Foundation of Shanghai(22ZR1460600)。
文摘A novel Eu^(3+)-doped fluorapatite red phosphor Ca_(2)Y_(8)(BO_(4))_(2)(SiO_(4))_(4)F_(2)Eu^(3+)with pure phase was synthesized in this study.Density functional theory(DFT)calculation and diffuse reflection spectrum analysis reveal its potential as a matrix for phosphors excited by ultraviolet light.Eu^(3+)has a^(7)F_(0)→^(5)L_(6)transition at 394 nm,and the prepared phosphor exhibits a high emission intensity at 614 nm,which may be attributed to the^(5)D_(0)-^(7)F_(2)energy transition at the lower symmetry site of Eu^(3+).The optimal doping concentration of the phosphor is determined to be 11 mol%,with concentration quenching attributed to the exchange interaction mechanism.The overall color purity of the phosphor is up to 99.88%,with an internal quantum efficiency as high as 91.15%.Notably,Ca_(2)Y_(8)(BO_(4))_(2)(SiO_(4))_(4)F_(2):11 mol%Eu^(3+)(CYBSF:11 mol%Eu^(3+))phosphors exhibit good thermal stability,with a thermal quenching temperature(T1/2)of 552 K and the intensity of emission at 423 K still at 88.89%of that at 298 K.The activation energy of the phosphor is up to 0.30287 eV.Its comprehensive luminescence performance surpasses that of commercial red phosphor,making it suitable for near ultraviolet excited warm white light emitting diode(NUV-WLED)with a high color rendering index(Ra=82)and a correlated color temperature(CCT)of 4339 K.Moreover,the phosphor achieves latent fingerprint visualization and anti-counterfeiting ink on different material surfaces:glass,aluminum foil,plastic and paper.Overall,the fluorapatite CYBSF:11 mol%Eu^(3+)phosphor holds great potential for multimodal applications due to its high quantum efficiency and good thermal stability.
基金supported by the National Key R&D Program of China (2021YFB3502902,2021YFB3503100,2022YFB3503300,2022YFB3505200)。
文摘The substitution of Fe by Co in the 2:14:1 phase is an effective method to increase the Curie temperature and enhance the thermal stability of the Nd-Fe-B magnets.However,the accumulation of Co ele ment at the grain boundaries(GBs) changes the GBs from nonmagnetic to ferromagnetic and causes the thinlayer GBs to become rare,In this paper,the method of diffusing Tb element was chosen to improve the microstructure and temperature stability of high-Co magnets.Three original sintered Nd_(28.5)Dy_(3)-CO_(x)e_(bal)M_(0.6)B_(i)(x=0,6 wt%,12 wt%;M = Cu,Al,Zr) magnets with different Co contents were diffused with Tb by grain boundary diffusion(GBD).After GBD,high-Co magnets exhibit more continuously distributed thin-layer GBs,and their thermal stability is significantly improved.In high-Co magnets(x=6 wt%),the absolute value of the temperature coefficient of coercivity decreases from 0.603%/K to0.508%/K in the temperature range of 293-413 K,that of remanence decreases from 0.099%/K to 0.091%/K,and the coercivity increases from 18.44 to 25.04 kOe.Transmission electron microscopy(TEM)characterization reveals that there are both the 1:2 phase and the amorphous phase in the high-Co magnet before and after GBD,EDS elemental analysis shows that Tb element is more likely to preferentially replace the rare earth elements in the 2:14:1 main phase than in the 1:2 phase and the amorphous phase.The concentration of Tb at the edge of the main phase is much higher than that in the 1:2phase and amorphous phase,which is beneficial to the improvement of the microstructure.The preferential replacement of Tb elements at the edge of the 2:14:1 phase and thin-layer GBs with a more continuous distribution are synergistically responsible for improving the thermal stability of high-Co magnets.The study indicates that GBD is an effective method to improve the microstructure and thermal stability of high-Co magnets.
基金funded by the Vietnam National University Ho Chi Minh City(VNU-HCM)under grant number C2022-18-41.
文摘This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The addition of non-halogen flame retardants(FRs)including aluminum trihydroxide(ATH),triphenyl phosphate(TPP),and diammonium phosphate(DAP)leads to markedly enhanced thermal sta-bility and fire resistance of the PU/nSiO_(2)/FRs nanocomposites,resulting in achieving UL-94 HB standard.In particular,the nanocomposites met the UL-94 V-0 criteria thanks to the inclusion of DAP at 25 phr.The LOI value of the nanocomposites reached 26%which is much higher than that of PU/nSiO_(2)nanocompos-ite,about 20%.In order to further understand the fire-proof mechanism,the residue char layer remaining of the PU/nSiO_(2)/FRs nanocomposites after being burned was also investigated by scanning electron mi-croscopy(SEM)and Fourier transform infrared(FTIR).In addition,the microstructure,thermal stability,thermal conductivity,and mechanical properties of nanocomposites were also evaluated in this study.
