SiOx is attractive as an anode material for lithium-ion batteries(LIBs)due to its high capacity,low cost,and relatively higher cyclic stability than Si anode.However,the intrinsic low electronic conductivity,low initi...SiOx is attractive as an anode material for lithium-ion batteries(LIBs)due to its high capacity,low cost,and relatively higher cyclic stability than Si anode.However,the intrinsic low electronic conductivity,low initial coulombic efficiency(ICE),and volume expansion during cycles hinder its applications.In this review,we summarize advances in high performance SiOx anodes,mainly from two aspects:active material and binders.The future perspective is investigated at the end of this review.Our review provides strategical guidance for developing high performance SiOx anodes.展开更多
Pore structure engineering has been acknowledged as suitable approach to creating active sites and en-hancing ion transport capabilities of hard carbon anodes.However,conventional porous carbon materials exhibit high ...Pore structure engineering has been acknowledged as suitable approach to creating active sites and en-hancing ion transport capabilities of hard carbon anodes.However,conventional porous carbon materials exhibit high BET and surface defects.Additionally,the sodium storage mechanism predominantly occurs in the slope region.This contradicts practical application requirements because the capacity of the plateau region is crucial for determining the actual capacity of batteries.In our work,we prepared a novel“core-shell”carbon framework(CNA1200).Introducingclosedporesand carboxylgroupsinto coal-basedcarbon materials to enhance its sodium storage performance.The closed pore structure dominates in the“core”structure,which is attributed to the timely removal of sodium hydroxide(NaOH)to prevent further for-mation of active carbon structure.The presence of closed pores is beneficial for increasing sodium ion storage in the low-voltage plateau region.And the“shell”structure originates from coal tar pitch,it not only uniformly connects hard carbon particles together to improve cycling stability,but is also rich in carboxyl groups to enhance the reversible sodium storage performance in slope region.CNA1200 has ex-cellent electrochemical performance,it exhibits a specific capacity of 335.2 mAh g^(−1)at a current density of 20 mA g^(−1)with ICE=51.53%.In addition,CNA1200 has outstanding cycling stability with a capac-ity retention of 91.8%even when cycling over 200 times.When CNA1200 is used as anode paired with Na_(3)V_(2)(PO_(4))_(3)cathode,it demonstrates a capacity of 109.54 mAh g^(−1)at 0.1 C and capacity retention of 94.64%at 0.5 C.This work provides valuable methods for regulating the structure of sodium-ion battery(SIBs)anode and enhances the potential for commercialization.展开更多
This study exhibits a design of the discharge product film of a bulk AZ63-Ce-La-Ca(AZ63X)anode for Mg-air battery.An ideal discharge product film for Mg anode is that it could inhibit the anodic hydrogen evolution but...This study exhibits a design of the discharge product film of a bulk AZ63-Ce-La-Ca(AZ63X)anode for Mg-air battery.An ideal discharge product film for Mg anode is that it could inhibit the anodic hydrogen evolution but does not hinder the transfer of the electrons at the interface.Fortunately,the addition of Ce,La,and Ca into AZ63 alloy achieves this goal.The Mg-air battery with AZ63X anode in 3.5%Na Cl has an ultrahigh anodic efficiency of 85.7±1.7%and energy-density of 2431±53 mWh g^(-1)with the unique discharge product film,surpassing the values of most reported Mg-air batteries.Furthermore,the alloying elements reduce the anode delamination effect significantly by transforming the block Mg_(17)Al_(12)phase into the connected Mg_(17)Al_(12)structure and fine rod Al_(2)RE and Al_(2)Ca.展开更多
Solid-state lighting is now developing toward high-power and super-brightness,but is largely limited by the lack of highly robust and efficient color conversion materials that can be survived from high-power or high-p...Solid-state lighting is now developing toward high-power and super-brightness,but is largely limited by the lack of highly robust and efficient color conversion materials that can be survived from high-power or high-power density excitation,typically the red-emitting ones.In this work,we fabricated highly effi-cient and pore-free Sr_(0.5)Ca_(0.5)AlSiN_(3)∶Eu^(2+)(SCASN)red-emitting ceramics by spark plasma sintering of fine phosphor powders.These fine phosphor powders were prepared by treating the commercial phosphors with high-energy ball-milling,centrifugation and acid washing,leading to a particle size of 2.55μm and an internal quantum efficiency as high as 74.0%under 450 nm excitation.The phosphor powders can be densified into SCASN ceramics without using sintering additives at a temperature as low as 1475℃,and the ceramics show an internal quantum efficiency of 75.3%,which is 50%higher than those ceram-ics fabricated with untreated commercial powders.When excited by a high-power blue LED at a current density of 4 A/mm^(2),the SCASN ceramics have a maximum luminous flux of 660 lm(i.e.,26 Mcd/m^(2)).The phosphor ceramics can also withstand a high laser power density of 15.7 W/mm^(2),and exhibit an output luminance of 188 Mcd/m^(2).This work provides a general method to prepare fine phosphor powders that enable to fabricate high efficiency phosphor ceramics used in high-power solid-state lighting.展开更多
The energy density of thin-film lithium batteries(TFLBs)is predominantly determined by the average voltage and specific capacity,however,the mechanism of regulating the voltage plateaus of the film electrodes is not w...The energy density of thin-film lithium batteries(TFLBs)is predominantly determined by the average voltage and specific capacity,however,the mechanism of regulating the voltage plateaus of the film electrodes is not well understood.In this study,three boride films(Co–B,Fe–B,and Co–Fe–B alloys)with different thick-nesses were fabricated to enhance the specific capacity and voltage stability of TFLBs.By analyzing the cycling performance,redox peak evolution,and capacitive contribution,the thickness-dependent lithiation behavior of the thin/thick films was elucidated.Theoretical simulations and electrochemical analysis were conducted to investigate how the lithiation behaviors affected the voltage profiles of the film electrodes.In addition,the various-thickness CoB films were compared in all-solid-state TFLBs,demonstrating the universality and practicability of this simple regulation strategy to develop high-performance energy storage devices.展开更多
Balancing high display performance with energy efficiency is crucial for global sustainability.Lowering operating frequencies—such as enabling 1 Hz operation in fringe-field switching(FFS)liquid crystal displays—red...Balancing high display performance with energy efficiency is crucial for global sustainability.Lowering operating frequencies—such as enabling 1 Hz operation in fringe-field switching(FFS)liquid crystal displays—reduces power consumption but is hindered by image flicker.While negative dielectric anisotropy liquid crystals(nLCs)mitigate flicker,their high driving voltages and production costs limit adoption.Positive dielectric anisotropy liquid crystals(pLCs)offer lower operating voltages,faster response times,and broader applicability,making them a more viable alternative.This study introduces a novel approach to minimizing flexoelectric effects in pLCs by investigating how single components influence flexoelectric behavior in mixtures through an effective experimental methodology.Two innovative measurement techniques—(1)flexoelectric coefficient difference analysis and(2)displacement-current measurement(DCM)—are presented,marking the first application of DCM for verifying flexoelectric effects.The proposed system eliminates uncertainties associated with previous methods,providing a reliable framework for selecting liquid crystal components with minimal flexoelectric effects while preserving key electro-optic properties.Given pLCs'higher reliability,lower production costs,and broader material selection,these advancements hold significant potential for low-power displays.We believe this work enhances flexoelectric analysis in nematic liquid crystals and contributes to sustainable innovation in the display industry,aligning with global energy-saving goals.展开更多
Magnesium-lithium hybrid batteries(MLHBs)have gained increasing attention due to their combined advantages of rapid ion insertion/extraction cathode and magnesium metal anode.Herein,Sn S_(2)-SPAN hybrid cathode with s...Magnesium-lithium hybrid batteries(MLHBs)have gained increasing attention due to their combined advantages of rapid ion insertion/extraction cathode and magnesium metal anode.Herein,Sn S_(2)-SPAN hybrid cathode with strong C-Sn bond and rich defects is ingeniously constructed to realize Mg^(2+)/Li^(+)co-intercalation.The physical and chemical double-confinement synergistic engineering of sulfurized polyacrylonitrile can suppress the agglomeration of Sn S_(2)nanoparticles and the volume expansion,simultaneously promote charge transfer and enhance structural stability.The introduced abundant sulfur vacancies provide more active sites for Mg^(2+)/Li^(+)co-intercalation.Meanwhile,the beneficial effects of rich sulfur defects and C-Sn bond on enhanced electrochemical properties are further evidenced by density-functional theory(DFT)calculations.Therefore,compared with pristine SnS_(2),SnS_(2)-SPAN cathode displays high specific capacity(218 m Ah g^(-1)at 0.5A g^(-1)over 700 cycles)and ultra-long cycling life(101 m Ah g^(-1)at 5 A g^(-1)up to 28,000 cycles).And a high energy density of 307 Wh kg^(-1)can be realized by the Sn S_(2)-SPAN//Mg pouch cell.Such elaborate and simple design supplies a reference for the exploitation of advanced cathode materials with excellent electrochemical properties for MLHBs.展开更多
Improving the high-temperature performance of Inconel 718(IN718)alloys manufactured via laser powder bed fusion(LPBF)has been the most concerned issue in the industry.In this study,the effects of Ti_(2)AlC inoculants ...Improving the high-temperature performance of Inconel 718(IN718)alloys manufactured via laser powder bed fusion(LPBF)has been the most concerned issue in the industry.In this study,the effects of Ti_(2)AlC inoculants on microstructures and high-temperature mechanical properties of the as-built IN718 composites were investigated.According to statistical results of relative density and unmelted particle area in as-built alloys,the optimal energy of 112 J/mm^(3)was determined.It was observed that the precipitation of the MC carbide was significantly enhanced with the addition of Ti_(2)AlC,restricting the precipitation of the Laves phase.The MC particles were uniformly distributed along the subgrain boundaries,which contributed to the dispersion strengthening.Meanwhile,the MC particles served as nucleation sites for heterogeneous nucleation during the solidification process,facilitating the refinement of columnar and cellular grains.The simulated Scheil-Gulliver curves showed that the precipitation sequence of phases did not change with Ti_(2)AlC inoculants.The as-built 1%Ti_(2)AlC/IN718 sample demonstrated an ultimate tensile strength of 998.78 MPa and an elongation of 18.04%at 650℃,revealing a markedly improved mechanical performance compared with the LPBF-manufactured IN718 alloys.The high-temperature tensile strength of 1%Ti_(2)AlC/IN718 sample increased to 1197.99 MPa by heat treatment.It was suggested that dislocation strengthening and ordered strengthening were two most important reinforcement mechanisms.展开更多
The stretching-induced phase transition of biodegradable poly(butylene succinate)(PBS)was explored using a combination of mechanical testing and in situ wide angle X-ray diffraction characterization.The phase transiti...The stretching-induced phase transition of biodegradable poly(butylene succinate)(PBS)was explored using a combination of mechanical testing and in situ wide angle X-ray diffraction characterization.The phase transition fromαphase toβphase can be effectively triggered by severe stretching,in which the threshold strain is dependent on the PBS crystallites.Interestingly,thisα-βphase transition can be reversed immediately once mechanical stretching begins to be released.It should be pointed out that the finish ofβ-αphase transition reversed,corresponding to the disappearance of the generatedβphase,does not necessarily need the external stretching to completely release.For the relaxation-reversed phase transition,the evolution of the normalizedβ-phase fraction exhibited a similar correlation with the stress released.It was indicated that the decay kinetics followed a stretching-dominant mechanism,and the amount ofβphase generated just prior to relaxation had a negligible influence on the reversed phase transition.展开更多
Zn-Al eutectoid alloy(ZA22)has ultra-high damping property,but its mechanical properties are still relatively low.In order to simultaneously improve the tensile strength and plasticity,a novel Al matrix composite inoc...Zn-Al eutectoid alloy(ZA22)has ultra-high damping property,but its mechanical properties are still relatively low.In order to simultaneously improve the tensile strength and plasticity,a novel Al matrix composite inoculant containing in-situ formed Al_(2)O_(3) and Al3Zr particles was designed and used to reinforce the ZA22 alloy.The microstructure of the ZA22 alloy was significantly refined.Fine Al_(2)O_(3) particles were uniformly distributed in theαphase and the lamellar eutectoid structure,whereas Al3Zr particles were distributed in theαphase and at theα/ηinterface.Property tests showed that the tensile mechanical properties of the reinforced ZA22 alloys were significantly improved.The maximum tensile strength and elongation reached 355 MPa and 7.62%,which were 1.50 and 1.89 times those of the original ZA22 alloy,respectively.The increase in mechanical properties is attributed to the multiple strengthening and toughening factors constructed in the refined microstructure.展开更多
As a typical eutectic high-entropy alloy(EHEA),AlCoCrFeNi2.1 exhibits excellent casting properties.However,the imbalance between strength and plasticity hinders its application as an advanced structural material.In or...As a typical eutectic high-entropy alloy(EHEA),AlCoCrFeNi2.1 exhibits excellent casting properties.However,the imbalance between strength and plasticity hinders its application as an advanced structural material.In order to address this challenge,deep cryogenic treatment(DCT)as a new process applied in the field of EHEAs was proposed in this study.The effects of different DCT times on the microstructure and mechanical properties of AlCoCrFeNi2.1 EHEAs were studied,mainly focusing on the flake structure of FCC+B2 layer.The experimental results suggest that with the extension of the DCT time,the dislocation density in the FCC phase increases significantly.The spherical BCC precipitate phase is generated within the B2 phase,and the average size of this newly generated precipitate phase gradually decreases.Increasing the number of dislocations and precipitate phases is of great significance to improve the mechanical properties.The AlCoCrFeNi2.1 EHEA exhibits excellent comprehensive mechanical properties after DCT for 36 h.Compared with the as-cast state,the tensile strength at room temperature reaches 1,034.51 MPa,increased by 5.74%.The plasticity reaches 21.72%,which is increased by 11.79%.The results show that the tensile strength and ductility of AlCoCrFeNi2.1 EHEAs are balanced and improved after DCT,which are more suitable as advanced structural materials.In addition,the introduction of the DCT process to EHEAs solves the problem of environmental pollution caused by traditional heat treatment process.This study provides useful guidance for using the DCT process to strengthen the mechanical properties of“lamellar+block”type EHEAs.展开更多
Heteroatom-doped porous carbon materials have been widely studied due to their high specific surface area and high heteroatom content,but it is difficult to achieve high specific surface area and high heteroatom conte...Heteroatom-doped porous carbon materials have been widely studied due to their high specific surface area and high heteroatom content,but it is difficult to achieve high specific surface area and high heteroatom content at the same time.Herein,a simple method is introduced to prepare N/O co-doped hierarchical porous carbon materials(DNZKs).Phthalonitrile resins(DNZs)were prepared by using 1,3-bis(3,4-dicyanophenoxy)benzene as raw material and ZnCl_(2)/urea as composite curing agent,and then using KOH as activator to successfully prepare DNZKs with high specific surface area,developed pores and high N/O content.The porous carbon material(DNZK@400)obtained at a curing temperature of 400℃ has the highest N content(4.97%(mass)),a large specific surface area(2026 m^(2)·g^(-1)),a high micropore proportion(0.9),a high O content(7.53%(mass)),and the best specific capacitance(up to 567 F·g^(-1) at 0.1 A·g^(-1)),which can be attribute to the high temperature resistance of the nitrogencontaining aromatic heterocyclic structure in DNZs.When the mass ratio of resin and KOH is 1:1,the specific capacitance of the sample tested by the acid three-electrode system is obtained,and it is found that the material has high cycling stability(119%specific capacitance retention after 100,000 cycle tests).This work proposes a simple and easy-to-operate method for the preparation of multifunctional porous carbon.展开更多
The design of low-cost and high-performance cyclic olefin copolymers remains challenging.Ethylene copolymers with dicyclopentadiene(DCPD)were prepared using Ph_(2)C(Cp)(Flu)ZrCl_(2)(Cat.1),rac-Et(Ind)_(2)ZrCl_(2)(Cat....The design of low-cost and high-performance cyclic olefin copolymers remains challenging.Ethylene copolymers with dicyclopentadiene(DCPD)were prepared using Ph_(2)C(Cp)(Flu)ZrCl_(2)(Cat.1),rac-Et(Ind)_(2)ZrCl_(2)(Cat.2),Me_(2)C(Cp)(Flu)ZrCl_(2)(Cat.3)andMe_(2)Si(Ind)_(2)ZrCl_(2)(Cat.4)combined with[Ph_(3)C][B(C_(6)F_(5))_(4)]/iBu_(3)Al.Ni(acac)_(2)/iBu_(3)Al was then used to catalyze the hydrogenation of the intracyclic double bonds of ethylene/DCPD copolymers.The results showed that compared to C_(2) symmetric catalysts(Cat.2 and Cat.4),Cs symmetric catalysts(Cat.1 and Cat.3)facilitated the incorporation of copolymers with higher DCPD.1H-and ^(13)C-NMR spectra indicated that ethylene/DCPD copolymerization occurred via enhancement of the norbornene ring.Additionally,measurement of the reactivity ratios provided further confirmation that the copolymers had random sequence distributions.All these samples demonstrated transmittance values above 90%in the visible wavelength range from 400 nm to 800 nm.By changing the fraction of monomers,the glass transition temperature,refractive index,Young's modulus,and tensile strength of the copolymer increased as the incorporation of DCPD increased,whereas the Abbe number and elongation at break decreased.Compared with ethylene/norbornene and ethylene/tetracyclicdodecene copolymers,ethylene/DCPD copolymers,with excellent optical and mechanical properties,are promising materials.展开更多
The commercial viability of lithium-sulfur batteries is still challenged by the notorious lithium polysulfides(Li PSs)shuttle effect on the sulfur cathode and uncontrollable Li dendrites growth on the Li anode.Herein,...The commercial viability of lithium-sulfur batteries is still challenged by the notorious lithium polysulfides(Li PSs)shuttle effect on the sulfur cathode and uncontrollable Li dendrites growth on the Li anode.Herein,a bi-service host with Co-Fe binary-metal selenide quantum dots embedded in three-dimensional inverse opal structured nitrogen-doped carbon skeleton(3DIO FCSe-QDs@NC)is elaborately designed for both sulfur cathode and Li metal anode.The highly dispersed FCSe-QDs with superb adsorptive-catalytic properties can effectively immobilize the soluble Li PSs and improve diffusion-conversion kinetics to mitigate the polysulfide-shutting behaviors.Simultaneously,the 3D-ordered porous networks integrated with abundant lithophilic sites can accomplish uniform Li deposition and homogeneous Li-ion flux for suppressing the growth of dendrites.Taking advantage of these merits,the assembled Li-S full batteries with 3DIO FCSe-QDs@NC host exhibit excellent rate performance and stable cycling ability(a low decay rate of 0.014%over 2,000 cycles at 2C).Remarkably,a promising areal capacity of 8.41 mAh cm^(-2)can be achieved at the sulfur loading up to 8.50 mg cm^(-2)with an ultra-low electrolyte/sulfur ratio of 4.1μL mg^(-1).This work paves the bi-serve host design from systematic experimental and theoretical analysis,which provides a viable avenue to solve the challenges of both sulfur and Li electrodes for practical Li-S full batteries.展开更多
To solve the environmental pollution and low yield during the sythesis of zeolitic imidazolate frameworks(ZIFs)and their derived materials,a KOH-assisted aqueous strategy is proposed to synthesize cobalt zeolitic imid...To solve the environmental pollution and low yield during the sythesis of zeolitic imidazolate frameworks(ZIFs)and their derived materials,a KOH-assisted aqueous strategy is proposed to synthesize cobalt zeolitic imidazolate framework(ZIF-67)polyhedrons,which are used as precursors to prepare cobalt selenide/carbon composites with different crystal phases(Co_(0.85)Se,CoSe_2).When evaluated as anode material for lithium ion batteries,Co_(0.85)Se/C composites deliver a reversible capacity of 758.7 m A·h·g^(-1)with a capacity retention rate of 90.5%at 1.0 A·g^(-1)after 500 cycles,and the superior rate capability is 620 m A·h·g^(-1)at 2.0 A·g^(-1).The addition of KOH accelerates the production of ZIF-67 crystals by boosting deprotonation of dimethylimidazole,resulting in rapid growth and structures transition from two-dimensional to three-dimensional of ZIF-67 in aqueous solution,which greatly promotes the application of MOFs in the field of energy storage and conversion.展开更多
Sulfur-rich polymers have gained a great deal of attention as the next-generation active materials in lithium-sulfur(Li-S)batteries due to their low cost,environmental compatibility,naturally sulfur uniform dispersion...Sulfur-rich polymers have gained a great deal of attention as the next-generation active materials in lithium-sulfur(Li-S)batteries due to their low cost,environmental compatibility,naturally sulfur uniform dispersion,and distinctive structure covalently bonding with sulfur atoms.However,the poor electrical conductivity and undesirable additional shuttle effect still hinder the commercial application of sulfur-rich polymers.Herein,we report a flexible semi-immobilization strategy to prepare allylterminated hyperbranched poly(ethyleneimine)-functionalized reduced graphene oxide(A-PEI-EGO)as sulfur-rich copolymer backbone.The semi-immobilization strategy can effectively reconcile the demand for polymer skeleton and conductive substrates through forming quaternary ammonium groups and reducing oxygen-containing functional groups,resulting in enhanced skeleton adsorption capacity and substrate electronic conductivity,respectively.Furthermore,the stable covalent bonding connection based on polymer molecules(A-PEI)not only completely prevents the additional shuttle effect of lithiation organic molecules and even sulfur-rich oligomers,but provides more inverse vulcanization active sites.As a result,the as-prepared A-PEI-EGO-S cathodes display an initial discharge capacity of1338 m A h g^(-1)at a rate of 0.1 C and an outstanding cycling stability of 0.046%capacity decay per cycle over 600 cycles.Even under 6.2 mg cm^(-2)S-loaded and sparing electrolyte of 6μL mg^(-1),the A-PEI-EGO-S cathode can also achieve a superior cycling performance of 98%capacity retention after 60 cycles,confirming its application potential.展开更多
The organic carbon source coating LiFe_(x)Mn_(1-x)PO_(4)suffers from the problem of non-uniform carbon cladding.Too thick carbon cladding layer instead hinders the de-embedding of lithium ions.In this paper,we choose ...The organic carbon source coating LiFe_(x)Mn_(1-x)PO_(4)suffers from the problem of non-uniform carbon cladding.Too thick carbon cladding layer instead hinders the de-embedding of lithium ions.In this paper,we choose cornstalk as the carbon source,then LiFe_(0.5)Mn_(0.5)PO_(4)@cornstalk-C(LFMP@C-C)with 3D anchoring structure is prepared by the solvothermal method.The results show that the LFMP with cornstalk as the carbon source has better performance compared to the sucrose-coated LFMP material(LFMP@C).The discharge capacity of LFMP@C-C is 116 mAh/g for the first cycle at 1 C and the capacity retention rate is 94.0%after 500 cycles,and the discharge capacity of LFMP@C-C is more than 17.17%higher than that of LFMP@C.展开更多
The capacitance performances of poly（3,4-ethylenedioxythiophene）-poly（styrenesulfonate）（PEDOT-PSS） supramolecular hydrogels have been investigated systematically. The materials show a specific capacitance of 67 ...The capacitance performances of poly（3,4-ethylenedioxythiophene）-poly（styrenesulfonate）（PEDOT-PSS） supramolecular hydrogels have been investigated systematically. The materials show a specific capacitance of 67 F/g and display excellent rate capability at the scan rate as high as 5000 m V/s in the cyclic voltammogram measurements, accompanied by good cycle stability. On the basis of the measurements of the microscale morphologies, specific areas and electrical conductivities, the mechanisms for the improvement of the electrochemical properties are discussed and ascribed to the novel porous microstructures of the hydrogels and the synergetic effect of the rigid PEDOT and soft PSS components. Furthermore, polyaniline（PAn） is compounded with the PEDOT-PSS hydrogels through an interfacial polymerization process, endowing the hydrogel materials with a higher specific capacitance of 160 F/g at the scan rate of 5000 m V/s. The significance of this work lies in the demonstration of a novel method to solve the problems of conducting polymers in electrochemical applications.展开更多
In this work,azobenzene mesogen-containing tin thiolates have been synthesized,which possess ordered lamellar structures persistent to higher temperature and serve as liquid crystalline precursors.Based on the preorga...In this work,azobenzene mesogen-containing tin thiolates have been synthesized,which possess ordered lamellar structures persistent to higher temperature and serve as liquid crystalline precursors.Based on the preorganized tin thiolate precursors,Sn S nanocrystals encapsulated with in-situ N-doped carbon layer have been achieved through a simple solventless pyrolysis process with the azobenzene mesogenic thiolate precursor served as Sn,S,N,and C sources simultaneously.Thus prepared nanocomposite materials as anode of lithium ion batteries present a large specific capacity of 604.6 m Ah·g^（-1）at a current density of 100 m A·g^（-1）,keeping a high capacity retention up to 96% after 80 cycles,and display high rate capability due to the synergistic effect of well-dispersed Sn S nanocrystals and N-doped carbon layer.Such encouraging results shed a light on the controlled preparation of advanced nanocomposites based on liquid crystalline metallomesogen precursors and may boost their novel intriguing applications.展开更多
In recent years, tungsten disulfide(WS_(2)) and tungsten selenide(WSe_(2)) have emerged as favorable electrode materials because of their high theoretical capacity, large interlayer spacing, and high chemical activity...In recent years, tungsten disulfide(WS_(2)) and tungsten selenide(WSe_(2)) have emerged as favorable electrode materials because of their high theoretical capacity, large interlayer spacing, and high chemical activity;nevertheless, they have relatively low electronic conductivity and undergo large volume expansion during cycling, which greatly hinder them in practical applications. These drawbacks are addressed by combining a superior type of carbon material, graphene, with WS_(2) and WSe_(2) to form a WS_(2)/WSe_(2)@graphene nanocomposites.These materials have received considerable attention in electro-chemical energy storage applications such as lithium-ion batteries(LIBs), sodium-ion batteries(SIBs),and supercapacitors. Considering the rapidly growing research enthusiasm on this topic over the past several years, here the recent progress of WS_(2)/WSe_(2)@graphene nanocomposites in electrochemical energy storage applications is summarized. Furthermore, various methods for the synthesis of WS_(2)/WSe_(2)@graphene nanocomposites are reported and the relationships among these methods, nano/microstructures, and electrochemical performance are systematically summarized and discussed. In addition, the challenges and prospects for the future study and application of WS_(2)/WSe_(2)@graphene nanocomposites in electrochemical energy storage applications are proposed.展开更多
基金National Natural Science Foundation of China(No.21905194)Natural Science Foundation of the Jiangsu Higher Education Institution of China(No.23KJB150032).
文摘SiOx is attractive as an anode material for lithium-ion batteries(LIBs)due to its high capacity,low cost,and relatively higher cyclic stability than Si anode.However,the intrinsic low electronic conductivity,low initial coulombic efficiency(ICE),and volume expansion during cycles hinder its applications.In this review,we summarize advances in high performance SiOx anodes,mainly from two aspects:active material and binders.The future perspective is investigated at the end of this review.Our review provides strategical guidance for developing high performance SiOx anodes.
基金the National Natural Science Foundation of China(No.21978164,22078189 and 22105120)the Outstanding Youth Science Fund of Shaanxi Province(No.2021JC-046)and the Special Support Program for high level talents of Shaanxi Province+3 种基金the Innovation Support Program of Shaanxi Province(2021JZY-001)the Key Research and Development Program of Shaanxi Province(No.2020GY-243)the Special Research Fund of Education Department of Shaanxi(No.20JK0535)the National High-end Foreign Expert Project(No.GDW20186100428).
文摘Pore structure engineering has been acknowledged as suitable approach to creating active sites and en-hancing ion transport capabilities of hard carbon anodes.However,conventional porous carbon materials exhibit high BET and surface defects.Additionally,the sodium storage mechanism predominantly occurs in the slope region.This contradicts practical application requirements because the capacity of the plateau region is crucial for determining the actual capacity of batteries.In our work,we prepared a novel“core-shell”carbon framework(CNA1200).Introducingclosedporesand carboxylgroupsinto coal-basedcarbon materials to enhance its sodium storage performance.The closed pore structure dominates in the“core”structure,which is attributed to the timely removal of sodium hydroxide(NaOH)to prevent further for-mation of active carbon structure.The presence of closed pores is beneficial for increasing sodium ion storage in the low-voltage plateau region.And the“shell”structure originates from coal tar pitch,it not only uniformly connects hard carbon particles together to improve cycling stability,but is also rich in carboxyl groups to enhance the reversible sodium storage performance in slope region.CNA1200 has ex-cellent electrochemical performance,it exhibits a specific capacity of 335.2 mAh g^(−1)at a current density of 20 mA g^(−1)with ICE=51.53%.In addition,CNA1200 has outstanding cycling stability with a capac-ity retention of 91.8%even when cycling over 200 times.When CNA1200 is used as anode paired with Na_(3)V_(2)(PO_(4))_(3)cathode,it demonstrates a capacity of 109.54 mAh g^(−1)at 0.1 C and capacity retention of 94.64%at 0.5 C.This work provides valuable methods for regulating the structure of sodium-ion battery(SIBs)anode and enhances the potential for commercialization.
基金supported by the National Natural Science Foundation of China(52471095)National Key Research and Development Program of China(Grant No.2023YFC2811404)Natural Science Foundation of Xiamen,China(No.3502Z20227015)。
文摘This study exhibits a design of the discharge product film of a bulk AZ63-Ce-La-Ca(AZ63X)anode for Mg-air battery.An ideal discharge product film for Mg anode is that it could inhibit the anodic hydrogen evolution but does not hinder the transfer of the electrons at the interface.Fortunately,the addition of Ce,La,and Ca into AZ63 alloy achieves this goal.The Mg-air battery with AZ63X anode in 3.5%Na Cl has an ultrahigh anodic efficiency of 85.7±1.7%and energy-density of 2431±53 mWh g^(-1)with the unique discharge product film,surpassing the values of most reported Mg-air batteries.Furthermore,the alloying elements reduce the anode delamination effect significantly by transforming the block Mg_(17)Al_(12)phase into the connected Mg_(17)Al_(12)structure and fine rod Al_(2)RE and Al_(2)Ca.
基金supported by the National Key Research and Development Program(MOST,No.2022YFE0108800)the National Natural Science Foundation of China(Nos.52272165,U2005213 and 52172157)the Major Science and Technology Projects of Xiamen Science and Technology Bureau(No.3502Z20231018).
文摘Solid-state lighting is now developing toward high-power and super-brightness,but is largely limited by the lack of highly robust and efficient color conversion materials that can be survived from high-power or high-power density excitation,typically the red-emitting ones.In this work,we fabricated highly effi-cient and pore-free Sr_(0.5)Ca_(0.5)AlSiN_(3)∶Eu^(2+)(SCASN)red-emitting ceramics by spark plasma sintering of fine phosphor powders.These fine phosphor powders were prepared by treating the commercial phosphors with high-energy ball-milling,centrifugation and acid washing,leading to a particle size of 2.55μm and an internal quantum efficiency as high as 74.0%under 450 nm excitation.The phosphor powders can be densified into SCASN ceramics without using sintering additives at a temperature as low as 1475℃,and the ceramics show an internal quantum efficiency of 75.3%,which is 50%higher than those ceram-ics fabricated with untreated commercial powders.When excited by a high-power blue LED at a current density of 4 A/mm^(2),the SCASN ceramics have a maximum luminous flux of 660 lm(i.e.,26 Mcd/m^(2)).The phosphor ceramics can also withstand a high laser power density of 15.7 W/mm^(2),and exhibit an output luminance of 188 Mcd/m^(2).This work provides a general method to prepare fine phosphor powders that enable to fabricate high efficiency phosphor ceramics used in high-power solid-state lighting.
基金supported by National Natural Science Foundation of China(Grant Nos.52101273 and U22A20118)Natural Science Foundation of Fujian Province of China(Grant No.2022J01042)Fundamental Research Funds for Central Universities of China(Grant No.20720242002).
文摘The energy density of thin-film lithium batteries(TFLBs)is predominantly determined by the average voltage and specific capacity,however,the mechanism of regulating the voltage plateaus of the film electrodes is not well understood.In this study,three boride films(Co–B,Fe–B,and Co–Fe–B alloys)with different thick-nesses were fabricated to enhance the specific capacity and voltage stability of TFLBs.By analyzing the cycling performance,redox peak evolution,and capacitive contribution,the thickness-dependent lithiation behavior of the thin/thick films was elucidated.Theoretical simulations and electrochemical analysis were conducted to investigate how the lithiation behaviors affected the voltage profiles of the film electrodes.In addition,the various-thickness CoB films were compared in all-solid-state TFLBs,demonstrating the universality and practicability of this simple regulation strategy to develop high-performance energy storage devices.
基金supported by Basic Science Research Program through the National Research Foundation(NRF)of Korea,funded by the Ministry of Science and ICT(MSIT),Korea[2022R1A2C2091671]by ITECH R&D Program of MOTIE/KEIT(Ministry of Trade,Industry&Energy/Korea Evaluation Institute of Industrial Technology)[20016808].
文摘Balancing high display performance with energy efficiency is crucial for global sustainability.Lowering operating frequencies—such as enabling 1 Hz operation in fringe-field switching(FFS)liquid crystal displays—reduces power consumption but is hindered by image flicker.While negative dielectric anisotropy liquid crystals(nLCs)mitigate flicker,their high driving voltages and production costs limit adoption.Positive dielectric anisotropy liquid crystals(pLCs)offer lower operating voltages,faster response times,and broader applicability,making them a more viable alternative.This study introduces a novel approach to minimizing flexoelectric effects in pLCs by investigating how single components influence flexoelectric behavior in mixtures through an effective experimental methodology.Two innovative measurement techniques—(1)flexoelectric coefficient difference analysis and(2)displacement-current measurement(DCM)—are presented,marking the first application of DCM for verifying flexoelectric effects.The proposed system eliminates uncertainties associated with previous methods,providing a reliable framework for selecting liquid crystal components with minimal flexoelectric effects while preserving key electro-optic properties.Given pLCs'higher reliability,lower production costs,and broader material selection,these advancements hold significant potential for low-power displays.We believe this work enhances flexoelectric analysis in nematic liquid crystals and contributes to sustainable innovation in the display industry,aligning with global energy-saving goals.
基金financially supported by the National Key R&D Program of China(No.2023YFB3809500)National Natural Science Foundation of China(Grant No.51931006,52272240 and U22A20118)+2 种基金the Fundamental Research Funds for the Central Universities of China(Xiamen University:No.20720220074)Science and Technology Projects of Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province(HRTP-[2022]-22)the“Double-First Class”Foundation of Materials Intelligent Manufacturing Discipline of Xiamen University。
文摘Magnesium-lithium hybrid batteries(MLHBs)have gained increasing attention due to their combined advantages of rapid ion insertion/extraction cathode and magnesium metal anode.Herein,Sn S_(2)-SPAN hybrid cathode with strong C-Sn bond and rich defects is ingeniously constructed to realize Mg^(2+)/Li^(+)co-intercalation.The physical and chemical double-confinement synergistic engineering of sulfurized polyacrylonitrile can suppress the agglomeration of Sn S_(2)nanoparticles and the volume expansion,simultaneously promote charge transfer and enhance structural stability.The introduced abundant sulfur vacancies provide more active sites for Mg^(2+)/Li^(+)co-intercalation.Meanwhile,the beneficial effects of rich sulfur defects and C-Sn bond on enhanced electrochemical properties are further evidenced by density-functional theory(DFT)calculations.Therefore,compared with pristine SnS_(2),SnS_(2)-SPAN cathode displays high specific capacity(218 m Ah g^(-1)at 0.5A g^(-1)over 700 cycles)and ultra-long cycling life(101 m Ah g^(-1)at 5 A g^(-1)up to 28,000 cycles).And a high energy density of 307 Wh kg^(-1)can be realized by the Sn S_(2)-SPAN//Mg pouch cell.Such elaborate and simple design supplies a reference for the exploitation of advanced cathode materials with excellent electrochemical properties for MLHBs.
基金supported by the National Natural Science Foundation of China(Nos.52374396 and 52122409).
文摘Improving the high-temperature performance of Inconel 718(IN718)alloys manufactured via laser powder bed fusion(LPBF)has been the most concerned issue in the industry.In this study,the effects of Ti_(2)AlC inoculants on microstructures and high-temperature mechanical properties of the as-built IN718 composites were investigated.According to statistical results of relative density and unmelted particle area in as-built alloys,the optimal energy of 112 J/mm^(3)was determined.It was observed that the precipitation of the MC carbide was significantly enhanced with the addition of Ti_(2)AlC,restricting the precipitation of the Laves phase.The MC particles were uniformly distributed along the subgrain boundaries,which contributed to the dispersion strengthening.Meanwhile,the MC particles served as nucleation sites for heterogeneous nucleation during the solidification process,facilitating the refinement of columnar and cellular grains.The simulated Scheil-Gulliver curves showed that the precipitation sequence of phases did not change with Ti_(2)AlC inoculants.The as-built 1%Ti_(2)AlC/IN718 sample demonstrated an ultimate tensile strength of 998.78 MPa and an elongation of 18.04%at 650℃,revealing a markedly improved mechanical performance compared with the LPBF-manufactured IN718 alloys.The high-temperature tensile strength of 1%Ti_(2)AlC/IN718 sample increased to 1197.99 MPa by heat treatment.It was suggested that dislocation strengthening and ordered strengthening were two most important reinforcement mechanisms.
基金supported by the National Natural Science Foundation of China(No.52273025).
文摘The stretching-induced phase transition of biodegradable poly(butylene succinate)(PBS)was explored using a combination of mechanical testing and in situ wide angle X-ray diffraction characterization.The phase transition fromαphase toβphase can be effectively triggered by severe stretching,in which the threshold strain is dependent on the PBS crystallites.Interestingly,thisα-βphase transition can be reversed immediately once mechanical stretching begins to be released.It should be pointed out that the finish ofβ-αphase transition reversed,corresponding to the disappearance of the generatedβphase,does not necessarily need the external stretching to completely release.For the relaxation-reversed phase transition,the evolution of the normalizedβ-phase fraction exhibited a similar correlation with the stress released.It was indicated that the decay kinetics followed a stretching-dominant mechanism,and the amount ofβphase generated just prior to relaxation had a negligible influence on the reversed phase transition.
基金supported by the Foundation Strengthening Program of China(No.2019-JCJQ-ZD-142-00)the Natural Science Foundation of Hebei Province,China(No.E2021202017)the Foundation of Guangdong Academy of Sciences,China(No.2021GDASYL-20210102002)。
文摘Zn-Al eutectoid alloy(ZA22)has ultra-high damping property,but its mechanical properties are still relatively low.In order to simultaneously improve the tensile strength and plasticity,a novel Al matrix composite inoculant containing in-situ formed Al_(2)O_(3) and Al3Zr particles was designed and used to reinforce the ZA22 alloy.The microstructure of the ZA22 alloy was significantly refined.Fine Al_(2)O_(3) particles were uniformly distributed in theαphase and the lamellar eutectoid structure,whereas Al3Zr particles were distributed in theαphase and at theα/ηinterface.Property tests showed that the tensile mechanical properties of the reinforced ZA22 alloys were significantly improved.The maximum tensile strength and elongation reached 355 MPa and 7.62%,which were 1.50 and 1.89 times those of the original ZA22 alloy,respectively.The increase in mechanical properties is attributed to the multiple strengthening and toughening factors constructed in the refined microstructure.
基金financially supported by the National Natural Science Foundation of China(Nos.52301061,52204394)the Joint Fund Project of Science and Technology Plan of Liaoning Province(No.2023-MSLH-250)the Science and the Technology Program of Liaoning Provincial Department of Education(No.JYTQN2023286)。
文摘As a typical eutectic high-entropy alloy(EHEA),AlCoCrFeNi2.1 exhibits excellent casting properties.However,the imbalance between strength and plasticity hinders its application as an advanced structural material.In order to address this challenge,deep cryogenic treatment(DCT)as a new process applied in the field of EHEAs was proposed in this study.The effects of different DCT times on the microstructure and mechanical properties of AlCoCrFeNi2.1 EHEAs were studied,mainly focusing on the flake structure of FCC+B2 layer.The experimental results suggest that with the extension of the DCT time,the dislocation density in the FCC phase increases significantly.The spherical BCC precipitate phase is generated within the B2 phase,and the average size of this newly generated precipitate phase gradually decreases.Increasing the number of dislocations and precipitate phases is of great significance to improve the mechanical properties.The AlCoCrFeNi2.1 EHEA exhibits excellent comprehensive mechanical properties after DCT for 36 h.Compared with the as-cast state,the tensile strength at room temperature reaches 1,034.51 MPa,increased by 5.74%.The plasticity reaches 21.72%,which is increased by 11.79%.The results show that the tensile strength and ductility of AlCoCrFeNi2.1 EHEAs are balanced and improved after DCT,which are more suitable as advanced structural materials.In addition,the introduction of the DCT process to EHEAs solves the problem of environmental pollution caused by traditional heat treatment process.This study provides useful guidance for using the DCT process to strengthen the mechanical properties of“lamellar+block”type EHEAs.
基金supported by the National Natural Science Foundation of China(51673033 and 52073038)the Fundamental Research Funds for the Central Universities(DUT22LAB605).
文摘Heteroatom-doped porous carbon materials have been widely studied due to their high specific surface area and high heteroatom content,but it is difficult to achieve high specific surface area and high heteroatom content at the same time.Herein,a simple method is introduced to prepare N/O co-doped hierarchical porous carbon materials(DNZKs).Phthalonitrile resins(DNZs)were prepared by using 1,3-bis(3,4-dicyanophenoxy)benzene as raw material and ZnCl_(2)/urea as composite curing agent,and then using KOH as activator to successfully prepare DNZKs with high specific surface area,developed pores and high N/O content.The porous carbon material(DNZK@400)obtained at a curing temperature of 400℃ has the highest N content(4.97%(mass)),a large specific surface area(2026 m^(2)·g^(-1)),a high micropore proportion(0.9),a high O content(7.53%(mass)),and the best specific capacitance(up to 567 F·g^(-1) at 0.1 A·g^(-1)),which can be attribute to the high temperature resistance of the nitrogencontaining aromatic heterocyclic structure in DNZs.When the mass ratio of resin and KOH is 1:1,the specific capacitance of the sample tested by the acid three-electrode system is obtained,and it is found that the material has high cycling stability(119%specific capacitance retention after 100,000 cycle tests).This work proposes a simple and easy-to-operate method for the preparation of multifunctional porous carbon.
基金supported by the National Natural Science Foundation of China(Nos.52130307 and 5240031453).
文摘The design of low-cost and high-performance cyclic olefin copolymers remains challenging.Ethylene copolymers with dicyclopentadiene(DCPD)were prepared using Ph_(2)C(Cp)(Flu)ZrCl_(2)(Cat.1),rac-Et(Ind)_(2)ZrCl_(2)(Cat.2),Me_(2)C(Cp)(Flu)ZrCl_(2)(Cat.3)andMe_(2)Si(Ind)_(2)ZrCl_(2)(Cat.4)combined with[Ph_(3)C][B(C_(6)F_(5))_(4)]/iBu_(3)Al.Ni(acac)_(2)/iBu_(3)Al was then used to catalyze the hydrogenation of the intracyclic double bonds of ethylene/DCPD copolymers.The results showed that compared to C_(2) symmetric catalysts(Cat.2 and Cat.4),Cs symmetric catalysts(Cat.1 and Cat.3)facilitated the incorporation of copolymers with higher DCPD.1H-and ^(13)C-NMR spectra indicated that ethylene/DCPD copolymerization occurred via enhancement of the norbornene ring.Additionally,measurement of the reactivity ratios provided further confirmation that the copolymers had random sequence distributions.All these samples demonstrated transmittance values above 90%in the visible wavelength range from 400 nm to 800 nm.By changing the fraction of monomers,the glass transition temperature,refractive index,Young's modulus,and tensile strength of the copolymer increased as the incorporation of DCPD increased,whereas the Abbe number and elongation at break decreased.Compared with ethylene/norbornene and ethylene/tetracyclicdodecene copolymers,ethylene/DCPD copolymers,with excellent optical and mechanical properties,are promising materials.
基金financial support from the National Natural Science Foundation of China(Grant Nos.51871188 and 51931006)the Fundamental Research Funds for the Central Universities of China(Xiamen University:Nos.20720200068,20720190007 and 20720220074)+2 种基金Guangdong Basic and Applied Basic Research Foundation(No.2021A1515010139)Science and Technology Projects of Innovation Laboratory for Sciences and Technologies of Energy Materials of Fujian Province(HRTP-[2022]-22)the“Double-First Class”Foundation of Materials Intelligent Manufacturing Discipline of Xiamen University。
文摘The commercial viability of lithium-sulfur batteries is still challenged by the notorious lithium polysulfides(Li PSs)shuttle effect on the sulfur cathode and uncontrollable Li dendrites growth on the Li anode.Herein,a bi-service host with Co-Fe binary-metal selenide quantum dots embedded in three-dimensional inverse opal structured nitrogen-doped carbon skeleton(3DIO FCSe-QDs@NC)is elaborately designed for both sulfur cathode and Li metal anode.The highly dispersed FCSe-QDs with superb adsorptive-catalytic properties can effectively immobilize the soluble Li PSs and improve diffusion-conversion kinetics to mitigate the polysulfide-shutting behaviors.Simultaneously,the 3D-ordered porous networks integrated with abundant lithophilic sites can accomplish uniform Li deposition and homogeneous Li-ion flux for suppressing the growth of dendrites.Taking advantage of these merits,the assembled Li-S full batteries with 3DIO FCSe-QDs@NC host exhibit excellent rate performance and stable cycling ability(a low decay rate of 0.014%over 2,000 cycles at 2C).Remarkably,a promising areal capacity of 8.41 mAh cm^(-2)can be achieved at the sulfur loading up to 8.50 mg cm^(-2)with an ultra-low electrolyte/sulfur ratio of 4.1μL mg^(-1).This work paves the bi-serve host design from systematic experimental and theoretical analysis,which provides a viable avenue to solve the challenges of both sulfur and Li electrodes for practical Li-S full batteries.
基金financially supported by the National Key Research and Development Program of China (2017YFA0208200)the National Natural Science Foundation of China (52102100,22022505 and 21872069)+4 种基金the Natural Science Foundation of Jiangsu Province (BK20181469)Guangdong Basic and Applied Basic Research Foundation (2020A1515110035)the Fundamental Research Funds for the Central Universities (0205-14380266,0205-14380272)the Scientific and Technological Innovation Special Fund for Carbon Peak and Carbon Neutrality of Jiangsu Province (BK20220008)the 2021 Suzhou Gusu Leading Talents of Science and Technology Innovation and Entrepreneurship in Wujiang District。
文摘To solve the environmental pollution and low yield during the sythesis of zeolitic imidazolate frameworks(ZIFs)and their derived materials,a KOH-assisted aqueous strategy is proposed to synthesize cobalt zeolitic imidazolate framework(ZIF-67)polyhedrons,which are used as precursors to prepare cobalt selenide/carbon composites with different crystal phases(Co_(0.85)Se,CoSe_2).When evaluated as anode material for lithium ion batteries,Co_(0.85)Se/C composites deliver a reversible capacity of 758.7 m A·h·g^(-1)with a capacity retention rate of 90.5%at 1.0 A·g^(-1)after 500 cycles,and the superior rate capability is 620 m A·h·g^(-1)at 2.0 A·g^(-1).The addition of KOH accelerates the production of ZIF-67 crystals by boosting deprotonation of dimethylimidazole,resulting in rapid growth and structures transition from two-dimensional to three-dimensional of ZIF-67 in aqueous solution,which greatly promotes the application of MOFs in the field of energy storage and conversion.
基金the support from National Outstanding Youth Science Fund (52222314)the CNPC Innovation Found (2021DQ02-1001)+2 种基金the Liao Ning Revitalization Talents Program (XLYC1907144)the Xinghai Talent Cultivation Plan (X20200303)the Fundamental Research Funds for the Central Universities (DUT22JC02,DUT22LAB605)。
文摘Sulfur-rich polymers have gained a great deal of attention as the next-generation active materials in lithium-sulfur(Li-S)batteries due to their low cost,environmental compatibility,naturally sulfur uniform dispersion,and distinctive structure covalently bonding with sulfur atoms.However,the poor electrical conductivity and undesirable additional shuttle effect still hinder the commercial application of sulfur-rich polymers.Herein,we report a flexible semi-immobilization strategy to prepare allylterminated hyperbranched poly(ethyleneimine)-functionalized reduced graphene oxide(A-PEI-EGO)as sulfur-rich copolymer backbone.The semi-immobilization strategy can effectively reconcile the demand for polymer skeleton and conductive substrates through forming quaternary ammonium groups and reducing oxygen-containing functional groups,resulting in enhanced skeleton adsorption capacity and substrate electronic conductivity,respectively.Furthermore,the stable covalent bonding connection based on polymer molecules(A-PEI)not only completely prevents the additional shuttle effect of lithiation organic molecules and even sulfur-rich oligomers,but provides more inverse vulcanization active sites.As a result,the as-prepared A-PEI-EGO-S cathodes display an initial discharge capacity of1338 m A h g^(-1)at a rate of 0.1 C and an outstanding cycling stability of 0.046%capacity decay per cycle over 600 cycles.Even under 6.2 mg cm^(-2)S-loaded and sparing electrolyte of 6μL mg^(-1),the A-PEI-EGO-S cathode can also achieve a superior cycling performance of 98%capacity retention after 60 cycles,confirming its application potential.
基金supported by CITIC Dameng Mining Industries Limited-Guangxi University Joint Research Institute of manganese resources utilization and advanced materials technology,Guangxi University-CITIC Dameng Mining Industries Limited Joint base of postgraduate cultivation,National Natural Science Foundation of China(No.11364003)Guangxi Innovation Driven Development Project(Nos.AA17204100,AA18118052)the Natural Science Foundation of Guangxi Province(No.2018GXNSFAA138186)。
文摘The organic carbon source coating LiFe_(x)Mn_(1-x)PO_(4)suffers from the problem of non-uniform carbon cladding.Too thick carbon cladding layer instead hinders the de-embedding of lithium ions.In this paper,we choose cornstalk as the carbon source,then LiFe_(0.5)Mn_(0.5)PO_(4)@cornstalk-C(LFMP@C-C)with 3D anchoring structure is prepared by the solvothermal method.The results show that the LFMP with cornstalk as the carbon source has better performance compared to the sucrose-coated LFMP material(LFMP@C).The discharge capacity of LFMP@C-C is 116 mAh/g for the first cycle at 1 C and the capacity retention rate is 94.0%after 500 cycles,and the discharge capacity of LFMP@C-C is more than 17.17%higher than that of LFMP@C.
基金financially supported by the National Natural Science Foundation of China(Nos.21174059 and 21374046)China Postdoctoral Science Foundation(No.2013M530249)+1 种基金Program for Changjiang Scholars and Innovative Research Teams in Universities,Open Project of State Key Laboratory of Superamolecular Structure and Materials(No.SKLSSM201416)the Testing Foundation of Nanjing University
文摘The capacitance performances of poly（3,4-ethylenedioxythiophene）-poly（styrenesulfonate）（PEDOT-PSS） supramolecular hydrogels have been investigated systematically. The materials show a specific capacitance of 67 F/g and display excellent rate capability at the scan rate as high as 5000 m V/s in the cyclic voltammogram measurements, accompanied by good cycle stability. On the basis of the measurements of the microscale morphologies, specific areas and electrical conductivities, the mechanisms for the improvement of the electrochemical properties are discussed and ascribed to the novel porous microstructures of the hydrogels and the synergetic effect of the rigid PEDOT and soft PSS components. Furthermore, polyaniline（PAn） is compounded with the PEDOT-PSS hydrogels through an interfacial polymerization process, endowing the hydrogel materials with a higher specific capacitance of 160 F/g at the scan rate of 5000 m V/s. The significance of this work lies in the demonstration of a novel method to solve the problems of conducting polymers in electrochemical applications.
基金Project supported by the National Natural Science Foundation of China(Grant No.21574062)the Huaian High-Technology Research Institute of Nanjing University,China(Grant No.2011Q1)
文摘In this work,azobenzene mesogen-containing tin thiolates have been synthesized,which possess ordered lamellar structures persistent to higher temperature and serve as liquid crystalline precursors.Based on the preorganized tin thiolate precursors,Sn S nanocrystals encapsulated with in-situ N-doped carbon layer have been achieved through a simple solventless pyrolysis process with the azobenzene mesogenic thiolate precursor served as Sn,S,N,and C sources simultaneously.Thus prepared nanocomposite materials as anode of lithium ion batteries present a large specific capacity of 604.6 m Ah·g^（-1）at a current density of 100 m A·g^（-1）,keeping a high capacity retention up to 96% after 80 cycles,and display high rate capability due to the synergistic effect of well-dispersed Sn S nanocrystals and N-doped carbon layer.Such encouraging results shed a light on the controlled preparation of advanced nanocomposites based on liquid crystalline metallomesogen precursors and may boost their novel intriguing applications.
基金financially supported by the National Key Research and Development Program of China (No.2020YFB1713500)the Chinese 02 Special Fund (No.2017ZX02408003)+5 种基金Open Fund of State Key Laboratory of Advanced Refractories (No.SKLAR202210)the Opening Project of National Joint Engineering Research Center for Abrasion Control and Molding of Metal Materials &Henan Key Laboratory of High-temperature Structural and Functional MaterialsHenan University of Science and Technology (No.HKDNM2019013)the Foundation of Department of Science and Technology of Henan Province (No.212102210219)the Student Research Training Plan of Henan University of Science and Technology (No.2021035)the Undergraduate Innovation and Entrepreneurship Training Program of Henan Province (No.S202110464005)。
文摘In recent years, tungsten disulfide(WS_(2)) and tungsten selenide(WSe_(2)) have emerged as favorable electrode materials because of their high theoretical capacity, large interlayer spacing, and high chemical activity;nevertheless, they have relatively low electronic conductivity and undergo large volume expansion during cycling, which greatly hinder them in practical applications. These drawbacks are addressed by combining a superior type of carbon material, graphene, with WS_(2) and WSe_(2) to form a WS_(2)/WSe_(2)@graphene nanocomposites.These materials have received considerable attention in electro-chemical energy storage applications such as lithium-ion batteries(LIBs), sodium-ion batteries(SIBs),and supercapacitors. Considering the rapidly growing research enthusiasm on this topic over the past several years, here the recent progress of WS_(2)/WSe_(2)@graphene nanocomposites in electrochemical energy storage applications is summarized. Furthermore, various methods for the synthesis of WS_(2)/WSe_(2)@graphene nanocomposites are reported and the relationships among these methods, nano/microstructures, and electrochemical performance are systematically summarized and discussed. In addition, the challenges and prospects for the future study and application of WS_(2)/WSe_(2)@graphene nanocomposites in electrochemical energy storage applications are proposed.
