For aqueous interfacial reactions involving H+and OH-, the interfacial pH varies dynamically during the reaction process, which is a key factor determining the reaction performance. Herein, the kinetic relevance betwe...For aqueous interfacial reactions involving H+and OH-, the interfacial pH varies dynamically during the reaction process, which is a key factor determining the reaction performance. Herein, the kinetic relevance between the interfacial pH and reaction rate is deciphered owing to the success in establishing the transport equations of H+/OH- in unbuffered solutions, and is charted as a current(j)–pH diagram in the form of an electrochemical response. The as-described j–pH interplay is experimentally verified by the oxygen reduction and hydrogen evolution reactions. This diagram serves to form a panoramic graphic view of pH function working on the interfacial reactions in conjunction with the Pourbaix’s potential–pH diagram, and particularly enables a kinetic understanding of the transport effect of H+and OH-on the reaction rate and valuable instruction toward associated pH control and buffering manipulation.展开更多
The interfacial reaction between Ti-6Al-4V alloy and ZrO2 ceramic mold with zirconia sol binder was investigated by keeping the 12 g alloy melt in a vacuum induction furnace for 15 s.The microstructures,element distri...The interfacial reaction between Ti-6Al-4V alloy and ZrO2 ceramic mold with zirconia sol binder was investigated by keeping the 12 g alloy melt in a vacuum induction furnace for 15 s.The microstructures,element distribution and phase constitution of the interface were identified by optical microscopy(OM),scanning electron microscopy(SEM)equipped with energy dispersive spectroscopy(EDS)and X-ray diffraction(XRD).The results show that the whole interface reaction layer can be divided into three regions:metal penetration layer,transition layer,and hardened layer according to the structure morphology,which has the characteristics of severe metal penetration,finer lamellar,and coarse oxygen-richαphase,respectively.The erosion of the alloy melt on the ceramic mold promotes the decomposition of zirconia,which leads to the increase of local Zr concentration,greatly increasing the activity coefficient of Ti,aggravating the occurrence of interfacial reaction.Thus,the interfacial reaction shows the characteristics of chain reaction.When the oxygen released by the dissolution of zirconia exceeds the local solid solubility,it precipitates in the form of bubbles,resulting in blowholes at the interface.The result also indicates that the zirconia mold with zirconia sol binder is not suitable for pouring heavy titanium alloy castings.展开更多
Diffusion couple experiments were performed to study the thermodynamic and kinetic mechanisms of interfacial reactions between the 316L stainless steel and the composite MnO-SiO_(2) oxide during isothermal heating at ...Diffusion couple experiments were performed to study the thermodynamic and kinetic mechanisms of interfacial reactions between the 316L stainless steel and the composite MnO-SiO_(2) oxide during isothermal heating at 1473 K(1200℃)for 1,3,5,and 10 h and at 1173,1273,1373,1473,and 1573 K(900,1000,1100,1200,and 1300℃)for 3 h.Compositional variations in the 316L stainless steel and the composite MnO-SiO_(2) oxide in the vicinity of the steel-oxide interface in each diffusion couple specimen were determined.Before and after isothermal heating,thermodynamic equilibria between the oxide and steel at the interface were estimated in accordance with the calculation of the Gibbs free energy change in the interfacial steel-oxide reactions.The diffusion coefficients of Mn,Cr,and Si in 316L stainless steel under different experimental conditions were quantitatively acquired.The results showed that solid-state interfacial reactions occurred between the Cr in the 316L stainless steel and composite MnO-SiO_(2) oxide during isothermal heating,which resulted in the depletion of Cr and accumulation of Si and Mn in the steel in the vicinity of the steel-oxide interface.The widths of the Crdepleted zone,Mn-accumulated zone and Si-accumulated zone all showed increasing trends with increasing isothermal heating temperature and time.The average values of the diffusion coefficients of Mn,Cr,and Si in the steel at 1473 K(1200℃)were 1.21×10^(^(-14))±2.96×10^(-15),1.69×10^(-14)±2.54×10^(-15),and 1.00×10^(-14)±1.96×10^(-15) m^(2)s^(-1),respectively,and they continued to increase with increasing isothermal heating temperature.展开更多
C_f/SiBCN ceramic composite was joined using Ni-19Cr-10Si(BNi5) and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 °C for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the C_f/SiBCN com...C_f/SiBCN ceramic composite was joined using Ni-19Cr-10Si(BNi5) and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 °C for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the C_f/SiBCN composite, with a contact angle of 13° and 4°, respectively. The microstructures of the brazed joints were investigated by electron-probe microanalysis(EPMA), and three-point bend test was conducted for the joints at room temperature. When being brazed with BNi5 filler alloy, no evident reaction layer was observed at the surface of the joined composite, and the joint microstructure was characterized by Ni_2Si matrix with scatteringly distributing mixture compounds of Cr_(23)C_6, Ni_2Si and CrB. While Ni-Cr-Pd(Si,B)brazing alloy was used, a Cr_(23)C_6 reaction layer with a thickness of 11 μm was formed at the surface of the base composite. In the central part of the brazed joint, the phases were composed of Ni(Cr,Si) solid solution and complex compounds including Pd_2Si,(Ni,Pd)_2Si and Ni-B. The strength of C_f/SiBCN joint brazed with BNi5 filler alloy was 62.9 MPa at room temperature, whereas that with Ni-Cr-Pd(Si,B) filler alloy was at the same level.展开更多
Silicon(Si)has been studied as a promising alloying type anode for lithium-ion batteries due to its high specific capacity,low operating potential and abundant resources.Nevertheless,huge volume expansion during alloy...Silicon(Si)has been studied as a promising alloying type anode for lithium-ion batteries due to its high specific capacity,low operating potential and abundant resources.Nevertheless,huge volume expansion during alloying/dealloying processes and low electronic conductivity of Si anodes restrict their electrochemical performance.Thus,carbon(C)materials with special physical and chemical properties are applied in Si anodes to effectively solve these problems.This review focuses on current status in the exploration of Si/C anodes,including the lithiation mechanism and solid electrolyte interface formation,various carbon sources in Si/C anodes,such as traditional carbon sources(graphite,pitch,biomass),and novel carbon sources(MXene,graphene,MOFs-derived carbon,graphdiyne,etc.),as well as interfacial bonding modes of Si and C in the Si/C anodes.Finally,we summarize and prospect the selection of carbonaceous materials,structural design and interface control of Si/C anodes,and application of Si/C anodes in all-solid-state lithium-ion batteries and sodium-ion batteries et al.This review will help researchers in the design of novel Si/C anodes for rechargeable batteries.展开更多
All-solid-state Li metal batteries(ASSLBs)using inorganic solid electrolyte(SE)are considered promising alternatives to conventional Li-ion batteries,offering improved safety and boosted energy density.While significa...All-solid-state Li metal batteries(ASSLBs)using inorganic solid electrolyte(SE)are considered promising alternatives to conventional Li-ion batteries,offering improved safety and boosted energy density.While significant progress has been made on improving the ionic conductivity of SEs,the degradation and instability of Li metal/inorganic SE interfaces have become the critical challenges that limit the coulombic efficiency,power performance,and cycling stability of ASSLBs.Understanding the mechanisms of complex/dynamic interfacial phenomena is of great importance in addressing these issues.Herein,recent studies on identifying,understanding,and solving interfacial issues on anode side in ASSLBs are comprehensively reviewed.Typical issues at Li metal/SE interface include Li dendrite growth/propagation,SE cracking,physical contact loss,and electrochemical reactions,which lead to high interfacial resistance and cell failure.The causes of these issues relating to the chemical,physical,and mechanical properties of Li metal and SEs are systematically discussed.Furthermore,effective mitigating strategies are summarized and their effects on suppressing interfacial reactions,improving interfacial Li-ion transport,maintaining interfacial contact,and stabilizing Li plating/stripping are highlighted.The in-depth mechanistic understanding of interfacial issues and complete investigations on current solutions provide foundations and guidance for future research and development to realize practical application of high-performance ASSLB.展开更多
Twin-roll casting has been recently revealed to be an effi cient technique to produce rejuvenated metallic glass(MG)strips.Due to the high melting point and high hardness,pure Mo is considered as a good roller materia...Twin-roll casting has been recently revealed to be an effi cient technique to produce rejuvenated metallic glass(MG)strips.Due to the high melting point and high hardness,pure Mo is considered as a good roller material as pure Cu.However,the wettability and interfacial reactions between MG melts and Cu or Mo remain largely unknown.In this work,a series of sessile droplet wetting experiments are designed to investigate the wettability and reactions between Zr_(41.2)Ti_(13.8)Cu_(12.5)Ni_(10)Be_(22.5)(Vit.1)or(Zr 0.401 Ti_(0.133)Cu_(0.118)Ni_(0.101)Be_(0.247))_(99)Nb_(1)(Nb1)MG melts and Cu/Mo substrates at temperatures of 1073,1123 and 1173 K.It is found that the wettability and interfacial reactions of the Vit.1 and Nb1 MG melts on the Cu substrates are very similar.The equilibrium contact angles are~30°at 1073 K and~25°-27°at 1123 K.The MG melts completely spread out on the Cu substrates at 1173 K.Cu substrates are slightly dissolved in the MG melts event at 1073 K,and a transitional reaction layer exists between the droplet and the Cu substrate.In comparison,the Vit.1 MG melt exhibits a much improved wettability on the Mo substrate.The equilibrium contact angle of the Vit.1/Mo is only 6°at 1073 K and 5°at 1123 K.No signifi cant diff usion of Mo into the droplet occurs even at 1173 K with a holding time of~30 min.The interfaces of the Vit.1/Mo samples are sharp,and no interfacial reaction layers form.These fi ndings indicate that pure Mo can be a good roller material for twin-roll casting at high temperatures,and the Mo-made rollers are expected of capability to produce MG strips with good quality.展开更多
Active soldering of 5A06 Al alloy was performed at 300 ℃ by using Sn-1Ti and Sn-1Ti-0.3Ga active solders, respectively. Theeffects of soldering time on the microstructure and mechanical properties of the joints were ...Active soldering of 5A06 Al alloy was performed at 300 ℃ by using Sn-1Ti and Sn-1Ti-0.3Ga active solders, respectively. Theeffects of soldering time on the microstructure and mechanical properties of the joints were investigated. The results showed that the Sn-1Tisolder broke the oxide film on the surface of the Al substrate and induced intergranular diffusion in the Al substrate. When Ga was added tothe solder, severe dissolution pits appeared in the Al substrate due to the action of Sn-1Ti-0.3Ga solder, and many Al particles were flakedfrom the matrix into the solder seam. Under thermal stress and the Ti adsorption effect, the oxide film cracked. With increasing solderingtime, the shear strength of 5A06 Al alloy joints soldered with Sn-1Ti and Sn-1Ti-0.3Ga active solders increased. When soldered for 90 min,the joint soldered with Sn-1Ti-0.3Ga solder had a higher shear strength of 22.12 MPa when compared to Sn-1Ti solder.展开更多
The tungsten particles reinforced Zr41.2Ti13.8Cu12.5Ni10Be22.5 (Vit 1 alloy) bulk metallic glass composites (BMGCs) were prepared by the melt infiltrating casting method with the infiltrating time of 1, 5 and 10 min, ...The tungsten particles reinforced Zr41.2Ti13.8Cu12.5Ni10Be22.5 (Vit 1 alloy) bulk metallic glass composites (BMGCs) were prepared by the melt infiltrating casting method with the infiltrating time of 1, 5 and 10 min, respectively. The changes of interfacial reaction and compression properties of the bulk metallic glass composites with different infiltrating times were studied. Results show that with the increase of infiltrating time, tiny nanocrystals are generated at the interfacial boundary of tungsten particles and the amorphous matrix, and the size of tiny crystals increases with the infiltrating time. When the infiltrating time is 10 min, polygonal crystals with a larger size are also generated within the amorphous matrix. The compressive strength of the composites also increases with the infiltrating time. When the infiltrating time is 10 min, the compressive strength of the composite reaches 2,030 MPa and the compression strain is 44%. The fracture morphology of the composite materials is in a vein-like pattern and the melting phenomenon is found on the fracture surface. In addition, the density of the shear bands during the compressive tests of the composite materials increases with the infiltrating time.展开更多
Anodic bonding of glass to Kovar alloy coated with Al film (Glass Al film/Kovar) was performed in the temperature range of 513 ～ 713?K under the static electric voltage of 500?V in order to investigate the interfacia...Anodic bonding of glass to Kovar alloy coated with Al film (Glass Al film/Kovar) was performed in the temperature range of 513 ～ 713?K under the static electric voltage of 500?V in order to investigate the interfacial phenomena of Al glass joint. The results reveal that Na and K ions within the glass are displaced by the applied field from the anode side surface of the glass to form depletion layers of them. The K ion depletion layer is narrow and followed by a K pile up layer, and both the two layers are formed within the Na depletion layer. The width of the Na and K depletion layers is increased with increasing bonding temperature and time. The activation energies for the growth of both depletion layers were close to that for Na diffusion in the glass. TEM observations reveal that Al film coated at the surface of Kovar alloy is oxidized to amorphous Al 2O 3 containing a few of Fe, Ni and Co by oxygen ions from the glass drifted by high electric field during bonding. The amount of Fe ions diffusing into the glass adjacent to the anode is significantly low due to the presence of Al film between Kovar alloy and the glass. As a result, the amorphous reaction layer of Fe Si O in the glass near the interface is avoided which is formed in Kovar glass joints.展开更多
The whisker/matrix interfaces in squeeze cast SiC w/AZ91 composites with different binders (silica binder, acid aluminum phosphate binder and without binder), were studied by transmission electron microscopy (TEM) and...The whisker/matrix interfaces in squeeze cast SiC w/AZ91 composites with different binders (silica binder, acid aluminum phosphate binder and without binder), were studied by transmission electron microscopy (TEM) and high resolution electron microscopy (HREM). The SiC w/AZ91 interface is very clean in the composites with no binders. For the composites with acid aluminum phosphate binders or silica binders, there exists fine discrete interfacial reaction products MgO at the interface, and a definite orientation relationship between MgO and SiC w. The interfacial reaction products MgO is unevenly distributed at different parts of the composite ingot with silica binder, and mainly distributed to the interface at the side part of the composite cylinder. While in the SiC w/AZ91 composite with acid aluminum phosphate binder, MgO particles are distributed evenly at the interface in almost all the parts of the composite ingot. [展开更多
Aqueous zinc(Zn)-ion batteries(AZIBs)are one of the most promising large-scale energy storage devices because of the excellent features of zinc metal anodes,including high theoretical capacity(5,855 mAh·cm^(–3)a...Aqueous zinc(Zn)-ion batteries(AZIBs)are one of the most promising large-scale energy storage devices because of the excellent features of zinc metal anodes,including high theoretical capacity(5,855 mAh·cm^(–3)and 820 mAh·g^(−1)),high safety,and natural abundance.Nevertheless,the large-scale applications of AZIBs are mainly limited by the severe interfacial side reactions of zinc metal anodes,which results in low plating/stripping Coulombic efficiency and poor cycling stability.To address this issue,we report an artificial Ta_(2)O_(5)protective layer on zinc foil(Ta_(2)O_(5)@Zn)for suppressing side reactions during Zn deposition/stripping.The results of density functional theory calculation and experiments indicate that Ta_(2)O_(5)@Zn anode can inhibit the side reactions between the electrolyte and zinc anode through the isolation effect.Benefiting from this advantage,the symmetric cells with Ta_(2)O_(5)@Zn anode delivered an ultralong lifespan of 3,000 h with a low overpotential at 0.25 mA·cm^(−2)for 0.05 mAh·cm^(−2).Furthermore,the full cells consisting of Ta_(2)O_(5)@Zn anode and MnO_(2)or NH_(4)V_(4)O_(10)cathode all present outstanding electrochemical performance,indicating its high reliability in practical applications.This strategy brings new opportunities for the future development of rechargeable AZIBs.展开更多
A novel melting infiltration by ultrasonic vibration was investigated and applied to fabricate Ti6Al4V(TC4)lattice structure-reinforced Mg-10Gd-2Y-1Zn-xZr(refer to VW92 hereafter,x=0,0.5 wt%)alloy matrix composites.Th...A novel melting infiltration by ultrasonic vibration was investigated and applied to fabricate Ti6Al4V(TC4)lattice structure-reinforced Mg-10Gd-2Y-1Zn-xZr(refer to VW92 hereafter,x=0,0.5 wt%)alloy matrix composites.The edge-to-edge matching model indicates that the well-matching and possible orientation relationships(ORs)between theα-Mg andα-Ti,[10-10]_(α-Mg)//[11-23]_(α-Ti) in(0002)_(α-Mg)//(10-10)_(α-Ti) possesses the smallest misfit of 0.4%(f_(r)),and thus theα-Mg grains can nucleate on the TC4 lattice structure.Interfacial reaction occurred in the TC4/VW92+0.5 wt%Zr composites,and the reaction product was confirmed to be Al_(2)Zr_(3),AlZr_(2) andα-Ti(Zr)particles formed by continuous solution of Zr-Ti.Among the interfacial products,the AlZr_(2) phase is a brittle phase with high-volume fraction,which is not conducive to the load transfer.But generally speaking,theα-Ti(Zr)and theα-Mg tend to form a coherent interface,which is beneficial for improving the interfacial bonding strength of composites.展开更多
The commercialization of nickel-rich LiNi_(0.8)Mn_(0.1)Co_(0.1)O_(2)(NMC811) has been hindered by its continuous loss of practical capacity and reduction in average working voltage.To address these issues,surface modi...The commercialization of nickel-rich LiNi_(0.8)Mn_(0.1)Co_(0.1)O_(2)(NMC811) has been hindered by its continuous loss of practical capacity and reduction in average working voltage.To address these issues,surface modification has been well-recognized as an effective strategy.Different from the coatings reported in literature to date,in this work,we for the first time report a sulfide coating,amorphous Li_(2)S via atomic layer deposition (ALD).Our study revealed that the conformal nano-Li_(2)S coating shows exceptional protection over the NMC811 cathodes,accounting for the dramatically boosted capacity retention from~11.6%to~71%and the evidently mitigated voltage reduction from 0.39 to 0.18 V after 500 charge–discharge cycles.In addition,the Li_(2)S coating remarkably improved the rate capability of the NMC811 cathode.Our investigation further revealed that all these beneficial effects of the ALD-deposited nano-Li_(2)S coating lie in the following aspects:(i) maintain the mechanical integrity of the NMC811 electrode:(ii) stabilize the NMC electrode/electrolyte interface:and (iii) suppress the irreversible phase transition of NMC structure.Particularly,this study also has revealed that the nano-Li_(2)S coating has played some unique role not associated with traditional non-sulfide coatings such as oxides.In this regard,we disclosed that the Li_(2)S layer has reacted with the released O_(2) from the NMC lattices,and thereby has dramatically mitigated electrolyte oxidation and electrode corrosion.Thus,this study is significant and has demonstrated that sulfides may be an important class of coating materials to tackle the issues of NMCs and other layered cathodes in lithium batteries.展开更多
The development of promising zinc anodes mainly suffers from their low plating/stripping coulombic efficiencies when using aqueous electrolyte,which are mainly associated with the interfacial formation of irreversible...The development of promising zinc anodes mainly suffers from their low plating/stripping coulombic efficiencies when using aqueous electrolyte,which are mainly associated with the interfacial formation of irreversible by-products.It is urgent to develop technologies that can solve this issue fundamentally.Herein,we report an artificial Sc_(2)O_(3) protective film to construct a new class of interface for Zn anode.The density functional theory simulation and experimental results have proven that the interfacial side reaction was inhibited via a stratified adsorption effect between this artificial layer and Zn anode.Benefiting from this novel structure,the Sc_(2)O_(3)-coated Zn anode can run for more than 100 cycles without short circuit and exhibit low voltage hysteresis,and the coulombic efficiency increases by 1.2%.Importantly,it shows a good application prospect when matched with two of popular manganese-based and vanadium-based cathodes.The excellent electrochemical performance of the Sc_(2)O_(3)-coated Zn anode highlights the importance of rational design of anode materials and demonstrates a good way for developing high-performance Zn anodes with long lifespan and high efficiency.展开更多
A novel liquid settling method was investigated and applied to fabricate TC4 spherical particle reinforced AZ91 alloy matrix composites.This method was called liquid state settling technique in which TC4 particles wou...A novel liquid settling method was investigated and applied to fabricate TC4 spherical particle reinforced AZ91 alloy matrix composites.This method was called liquid state settling technique in which TC4 particles would settle down under the force of gravity.High volume fraction(50%)particle reinforced AZ91 composites could be easily obtained via this novel method.This is difficult to achieve for other traditional liquid fabrication methods.In addition,there was a good dispersion of TC4 particles in the AZ91 matrix and no clusters were found,which indicate that this method was feasible.Interfacial reaction occurred and the reaction product was confirmed to be Al2Ti.Three kinds of pre-dispersion technologies were used before the settling process and different interfacial microstructures were found.Theoretical calculation and experimental results both indicated that the interfacial product which was embedded in the matrix strengthened the composites and improved the tensile strength.展开更多
Au nanostructures were prepared on uniform Cu_2O octahedra and rhombic dodecahedra via the galvanic replacement reaction between HAu Cl4 and Cu2O. The compositions and structures were studied by Scanning Electron Micr...Au nanostructures were prepared on uniform Cu_2O octahedra and rhombic dodecahedra via the galvanic replacement reaction between HAu Cl4 and Cu2O. The compositions and structures were studied by Scanning Electron Microscope(SEM), Transmission Electron Microscope(TEM), High-Resolution Transmission Electron Microscope(HRTEM), X-Ray Diffraction(XRD), X-Ray Absorption Spectroscopy(XAS), X-ray Photoelectron Spectroscopy(XPS) and in-situ DRIFTS spectroscopy of CO adsorption. Different from the formation of Au–Cu alloys on Cu_2O cubes by the galvanic replacement reaction(Chem Nano Mat 2(2016)861-865), metallic Au particles and positively-charged Au clusters form on Cu_2O octahedra and rhombic dodecahedra at very small Au loadings and only metallic Au particles form at large Au loadings. Metallic Au particles on Cu_2O octahedra and rhombic dodecahedra are more active in catalyzing the liquid phase aerobic oxidation reaction of benzyl alcohol than positively-charged Au clusters. These results demonstrate an obvious morphology effect of Cu_2O nanocrystals on the liquid–solid interfacial reactions and prove oxide morphology as an effective strategy to tune the surface reactivity and catalytic performance.展开更多
Ti_(3)AlC_(2)-reinforced Ag-based composites,which are used as sliding current collectors,electrical contacts,and electrode materials,exhibit remarkable performances.However,the interfacial reactions between Ag and Ti...Ti_(3)AlC_(2)-reinforced Ag-based composites,which are used as sliding current collectors,electrical contacts,and electrode materials,exhibit remarkable performances.However,the interfacial reactions between Ag and Ti_(3)AlC_(2) significantly degrade the electrical and thermal properties of these composites.To diminish these interfacial reactions,we fabricated carbon-coated Ti_(3)AlC_(2) particles(C@Ti_(3)AlC_(2))as reinforcement and prepared Ag–10wt%C@Ti_(3)AlC_(2) composites with carbon-layer thicknesses ranging from 50–200 nm.Compared with the uncoated Ag–Ti_(3)AlC_(2) composite,Ag–C@Ti_(3)AlC_(2) was found to have a better distribution of Ti_(3)AlC_(2) particles.With increases in the carbon-layer thickness,the Vickers hardness value and relative density of Ag–C@Ti_(3)AlC_(2) gradually decreases.With a carbon-layer thickness of 150 nm,we obtained the lowest resistivity of Ag–C@Ti_(3)AlC_(2) of 29.4135.5×10^(−9)Ω·m,which is half that of Ag–Ti_(3)AlC_(2)(66.7×10^(−9)Ω·m).The thermal conductivity of Ag–C@Ti_(3)AlC_(2) reached a maximum value of 135.5 W·m^(−1)·K^(−1) with a 200-nm carbon coating(~1.8 times that of Ag–Ti_(3)AlC_(2)).These results indicate that the carbon-coating method is a feasible strategy for improving the performance of Ag–C@Ti_(3)AlC_(2) composites.展开更多
Lean electrolyte usage in lithium–sulfur battery(LSB)meets the demand of the high energy density.However,lean condition makes the electrolyte-related interface discrete,leading to retardation of ion transfer that dep...Lean electrolyte usage in lithium–sulfur battery(LSB)meets the demand of the high energy density.However,lean condition makes the electrolyte-related interface discrete,leading to retardation of ion transfer that depends on interfaces.Consequently,electrochemical reactions face restraint.Herein,lithium polyacrylate acid(LiPAA)with short-chain anions(molecular weight of 2000)is introduced into the cathode.Because of the polysulfide(PS)-philic instinct of the short-chain PAA anions,short-chain PS is captured inside of the cathode.In addition,LiPAA supplies Li^(+)to the short-chain PS captured.The strong interaction between Li_(2)S_(4)and LiPAA effectively decreases Li_(2)S_(4)migration to the anode during discharging.In a sense,the ion mass transfer pattern is thus changed comparing to traditional long-way mode between cathode and anode.Galvanostatic intermittent titration technique(GITT)proves that the interfacial reaction resistance is greatly decreased in the region where Li_(2)S_(x)(x≤4)reduction contributes most.In the same time,the reversibility of electrochemical reduction/oxidation is improved.Owing to the accelerated Li_(2)S_(x)(x≤4)reduction,Li implanting of only 0.3 wt.%plus O introduction up to 1.4 wt.%enables the LSB perform well even with 1/4 of regular electrolyte dosage(5μL mg^(-1))and high-sulfur loading(4.2 mg cm^(-2)),increasing its rate capacity C_(0.8/0.5)from 52.6%(without the LiPAA)to 92.3%(with the LiP AA)as well as a capacity of 518.7 mAh g^(-1)after 400 cycles at 0.8 mA cm^(-2).展开更多
基金the National Natural Science Foundation of China(51525805,51727812,51808526)。
文摘For aqueous interfacial reactions involving H+and OH-, the interfacial pH varies dynamically during the reaction process, which is a key factor determining the reaction performance. Herein, the kinetic relevance between the interfacial pH and reaction rate is deciphered owing to the success in establishing the transport equations of H+/OH- in unbuffered solutions, and is charted as a current(j)–pH diagram in the form of an electrochemical response. The as-described j–pH interplay is experimentally verified by the oxygen reduction and hydrogen evolution reactions. This diagram serves to form a panoramic graphic view of pH function working on the interfacial reactions in conjunction with the Pourbaix’s potential–pH diagram, and particularly enables a kinetic understanding of the transport effect of H+and OH-on the reaction rate and valuable instruction toward associated pH control and buffering manipulation.
基金the National Natural Science Foundation of China(Grant No.51871184)the Natural Science Foundation of Shandong Province(Grant No.ZR2017MEE038)China Postdoctoral Science Foundation(No.2018M642683)。
文摘The interfacial reaction between Ti-6Al-4V alloy and ZrO2 ceramic mold with zirconia sol binder was investigated by keeping the 12 g alloy melt in a vacuum induction furnace for 15 s.The microstructures,element distribution and phase constitution of the interface were identified by optical microscopy(OM),scanning electron microscopy(SEM)equipped with energy dispersive spectroscopy(EDS)and X-ray diffraction(XRD).The results show that the whole interface reaction layer can be divided into three regions:metal penetration layer,transition layer,and hardened layer according to the structure morphology,which has the characteristics of severe metal penetration,finer lamellar,and coarse oxygen-richαphase,respectively.The erosion of the alloy melt on the ceramic mold promotes the decomposition of zirconia,which leads to the increase of local Zr concentration,greatly increasing the activity coefficient of Ti,aggravating the occurrence of interfacial reaction.Thus,the interfacial reaction shows the characteristics of chain reaction.When the oxygen released by the dissolution of zirconia exceeds the local solid solubility,it precipitates in the form of bubbles,resulting in blowholes at the interface.The result also indicates that the zirconia mold with zirconia sol binder is not suitable for pouring heavy titanium alloy castings.
基金supported by the National Natural Science Foundation of China(Grant Nos.U21A20113 and 52074198)also supported by the Project for Technology Talents ServinggEnterprises of Hubei Province(Grant No.KJRQ2023000073).
文摘Diffusion couple experiments were performed to study the thermodynamic and kinetic mechanisms of interfacial reactions between the 316L stainless steel and the composite MnO-SiO_(2) oxide during isothermal heating at 1473 K(1200℃)for 1,3,5,and 10 h and at 1173,1273,1373,1473,and 1573 K(900,1000,1100,1200,and 1300℃)for 3 h.Compositional variations in the 316L stainless steel and the composite MnO-SiO_(2) oxide in the vicinity of the steel-oxide interface in each diffusion couple specimen were determined.Before and after isothermal heating,thermodynamic equilibria between the oxide and steel at the interface were estimated in accordance with the calculation of the Gibbs free energy change in the interfacial steel-oxide reactions.The diffusion coefficients of Mn,Cr,and Si in 316L stainless steel under different experimental conditions were quantitatively acquired.The results showed that solid-state interfacial reactions occurred between the Cr in the 316L stainless steel and composite MnO-SiO_(2) oxide during isothermal heating,which resulted in the depletion of Cr and accumulation of Si and Mn in the steel in the vicinity of the steel-oxide interface.The widths of the Crdepleted zone,Mn-accumulated zone and Si-accumulated zone all showed increasing trends with increasing isothermal heating temperature and time.The average values of the diffusion coefficients of Mn,Cr,and Si in the steel at 1473 K(1200℃)were 1.21×10^(^(-14))±2.96×10^(-15),1.69×10^(-14)±2.54×10^(-15),and 1.00×10^(-14)±1.96×10^(-15) m^(2)s^(-1),respectively,and they continued to increase with increasing isothermal heating temperature.
基金financially supported by the National Natural Science Foundation of China (Contract Nos. 59905022, 50475160 and 51275497)Aeronautical Science Foundation of China (Grant 2008 ZE21005)
文摘C_f/SiBCN ceramic composite was joined using Ni-19Cr-10Si(BNi5) and Ni-33Cr-24Pd-3.5Si-0.5B filler alloys at 1170 °C for 10 min. Two kinds of Ni-based filler alloys exhibited good wettability on the C_f/SiBCN composite, with a contact angle of 13° and 4°, respectively. The microstructures of the brazed joints were investigated by electron-probe microanalysis(EPMA), and three-point bend test was conducted for the joints at room temperature. When being brazed with BNi5 filler alloy, no evident reaction layer was observed at the surface of the joined composite, and the joint microstructure was characterized by Ni_2Si matrix with scatteringly distributing mixture compounds of Cr_(23)C_6, Ni_2Si and CrB. While Ni-Cr-Pd(Si,B)brazing alloy was used, a Cr_(23)C_6 reaction layer with a thickness of 11 μm was formed at the surface of the base composite. In the central part of the brazed joint, the phases were composed of Ni(Cr,Si) solid solution and complex compounds including Pd_2Si,(Ni,Pd)_2Si and Ni-B. The strength of C_f/SiBCN joint brazed with BNi5 filler alloy was 62.9 MPa at room temperature, whereas that with Ni-Cr-Pd(Si,B) filler alloy was at the same level.
基金supported by the National Natural Science Foundation of China(5197219862133007)the Taishan Scholars Program of Shandong Province(tsqn201812002,ts20190908)+1 种基金the Shenzhen Fundamental Research Program(JCYJ20190807093405503)The Natural Science Foundation of Shandong Province(No.ZR2020JQ19)。
文摘Silicon(Si)has been studied as a promising alloying type anode for lithium-ion batteries due to its high specific capacity,low operating potential and abundant resources.Nevertheless,huge volume expansion during alloying/dealloying processes and low electronic conductivity of Si anodes restrict their electrochemical performance.Thus,carbon(C)materials with special physical and chemical properties are applied in Si anodes to effectively solve these problems.This review focuses on current status in the exploration of Si/C anodes,including the lithiation mechanism and solid electrolyte interface formation,various carbon sources in Si/C anodes,such as traditional carbon sources(graphite,pitch,biomass),and novel carbon sources(MXene,graphene,MOFs-derived carbon,graphdiyne,etc.),as well as interfacial bonding modes of Si and C in the Si/C anodes.Finally,we summarize and prospect the selection of carbonaceous materials,structural design and interface control of Si/C anodes,and application of Si/C anodes in all-solid-state lithium-ion batteries and sodium-ion batteries et al.This review will help researchers in the design of novel Si/C anodes for rechargeable batteries.
基金supported by the Outstanding Youth Fund Project by the Department of Science and Technology of Jiangsu Province(Grant No.BK20220045)the Key R&D Project funded by the Department of Science and Technology of Jiangsu Province(Grant No.BE2020003)+6 种基金Key Program-Automobile Joint Fund of National Natural Science Foundation of China(Grant No.U1964205)General Program of National Natural Science Foundation of China(Grant No.51972334)General Program of National Natural Science Foundation of Beijing(Grant No.2202058)Cultivation project of leading innovative experts in Changzhou City(CQ20210003)National Overseas High-level Expert recruitment Program(Grant No.E1JF021E11)Talent Program of Chinese Academy of Sciences,“Scientist Studio Program Funding”from Yangtze River Delta Physics Research Center,and Tianmu Lake Institute of Advanced Energy Storage Technologies(Grant No.TIESSS0001)Science and Technology Research Institute of China Three Gorges Corporation(Grant No.202103402)
文摘All-solid-state Li metal batteries(ASSLBs)using inorganic solid electrolyte(SE)are considered promising alternatives to conventional Li-ion batteries,offering improved safety and boosted energy density.While significant progress has been made on improving the ionic conductivity of SEs,the degradation and instability of Li metal/inorganic SE interfaces have become the critical challenges that limit the coulombic efficiency,power performance,and cycling stability of ASSLBs.Understanding the mechanisms of complex/dynamic interfacial phenomena is of great importance in addressing these issues.Herein,recent studies on identifying,understanding,and solving interfacial issues on anode side in ASSLBs are comprehensively reviewed.Typical issues at Li metal/SE interface include Li dendrite growth/propagation,SE cracking,physical contact loss,and electrochemical reactions,which lead to high interfacial resistance and cell failure.The causes of these issues relating to the chemical,physical,and mechanical properties of Li metal and SEs are systematically discussed.Furthermore,effective mitigating strategies are summarized and their effects on suppressing interfacial reactions,improving interfacial Li-ion transport,maintaining interfacial contact,and stabilizing Li plating/stripping are highlighted.The in-depth mechanistic understanding of interfacial issues and complete investigations on current solutions provide foundations and guidance for future research and development to realize practical application of high-performance ASSLB.
基金financially supported by the National Natural Science Foundation of China(Nos.51790484 and 52171164)the National Key Research and Development Program of China(No.2018YFB0703402)+3 种基金the Science and Technology on Transient Impact Laboratory(6142606192208)Liaoning Revitalization Talents Program(Nos.XLYC1802078 and XLYC1807062)the Chinese Academy of Sciences(No.ZDBS-LY-JSC023)the Youth Innovation Promotion Association CAS(No.2021188)。
文摘Twin-roll casting has been recently revealed to be an effi cient technique to produce rejuvenated metallic glass(MG)strips.Due to the high melting point and high hardness,pure Mo is considered as a good roller material as pure Cu.However,the wettability and interfacial reactions between MG melts and Cu or Mo remain largely unknown.In this work,a series of sessile droplet wetting experiments are designed to investigate the wettability and reactions between Zr_(41.2)Ti_(13.8)Cu_(12.5)Ni_(10)Be_(22.5)(Vit.1)or(Zr 0.401 Ti_(0.133)Cu_(0.118)Ni_(0.101)Be_(0.247))_(99)Nb_(1)(Nb1)MG melts and Cu/Mo substrates at temperatures of 1073,1123 and 1173 K.It is found that the wettability and interfacial reactions of the Vit.1 and Nb1 MG melts on the Cu substrates are very similar.The equilibrium contact angles are~30°at 1073 K and~25°-27°at 1123 K.The MG melts completely spread out on the Cu substrates at 1173 K.Cu substrates are slightly dissolved in the MG melts event at 1073 K,and a transitional reaction layer exists between the droplet and the Cu substrate.In comparison,the Vit.1 MG melt exhibits a much improved wettability on the Mo substrate.The equilibrium contact angle of the Vit.1/Mo is only 6°at 1073 K and 5°at 1123 K.No signifi cant diff usion of Mo into the droplet occurs even at 1173 K with a holding time of~30 min.The interfaces of the Vit.1/Mo samples are sharp,and no interfacial reaction layers form.These fi ndings indicate that pure Mo can be a good roller material for twin-roll casting at high temperatures,and the Mo-made rollers are expected of capability to produce MG strips with good quality.
基金the National Natural Science Foundation of China(No.52171045).
文摘Active soldering of 5A06 Al alloy was performed at 300 ℃ by using Sn-1Ti and Sn-1Ti-0.3Ga active solders, respectively. Theeffects of soldering time on the microstructure and mechanical properties of the joints were investigated. The results showed that the Sn-1Tisolder broke the oxide film on the surface of the Al substrate and induced intergranular diffusion in the Al substrate. When Ga was added tothe solder, severe dissolution pits appeared in the Al substrate due to the action of Sn-1Ti-0.3Ga solder, and many Al particles were flakedfrom the matrix into the solder seam. Under thermal stress and the Ti adsorption effect, the oxide film cracked. With increasing solderingtime, the shear strength of 5A06 Al alloy joints soldered with Sn-1Ti and Sn-1Ti-0.3Ga active solders increased. When soldered for 90 min,the joint soldered with Sn-1Ti-0.3Ga solder had a higher shear strength of 22.12 MPa when compared to Sn-1Ti solder.
基金This work was supported by the Liaoning Joint Fund of NSFC(No.U1908219).
文摘The tungsten particles reinforced Zr41.2Ti13.8Cu12.5Ni10Be22.5 (Vit 1 alloy) bulk metallic glass composites (BMGCs) were prepared by the melt infiltrating casting method with the infiltrating time of 1, 5 and 10 min, respectively. The changes of interfacial reaction and compression properties of the bulk metallic glass composites with different infiltrating times were studied. Results show that with the increase of infiltrating time, tiny nanocrystals are generated at the interfacial boundary of tungsten particles and the amorphous matrix, and the size of tiny crystals increases with the infiltrating time. When the infiltrating time is 10 min, polygonal crystals with a larger size are also generated within the amorphous matrix. The compressive strength of the composites also increases with the infiltrating time. When the infiltrating time is 10 min, the compressive strength of the composite reaches 2,030 MPa and the compression strain is 44%. The fracture morphology of the composite materials is in a vein-like pattern and the melting phenomenon is found on the fracture surface. In addition, the density of the shear bands during the compressive tests of the composite materials increases with the infiltrating time.
文摘Anodic bonding of glass to Kovar alloy coated with Al film (Glass Al film/Kovar) was performed in the temperature range of 513 ～ 713?K under the static electric voltage of 500?V in order to investigate the interfacial phenomena of Al glass joint. The results reveal that Na and K ions within the glass are displaced by the applied field from the anode side surface of the glass to form depletion layers of them. The K ion depletion layer is narrow and followed by a K pile up layer, and both the two layers are formed within the Na depletion layer. The width of the Na and K depletion layers is increased with increasing bonding temperature and time. The activation energies for the growth of both depletion layers were close to that for Na diffusion in the glass. TEM observations reveal that Al film coated at the surface of Kovar alloy is oxidized to amorphous Al 2O 3 containing a few of Fe, Ni and Co by oxygen ions from the glass drifted by high electric field during bonding. The amount of Fe ions diffusing into the glass adjacent to the anode is significantly low due to the presence of Al film between Kovar alloy and the glass. As a result, the amorphous reaction layer of Fe Si O in the glass near the interface is avoided which is formed in Kovar glass joints.
文摘The whisker/matrix interfaces in squeeze cast SiC w/AZ91 composites with different binders (silica binder, acid aluminum phosphate binder and without binder), were studied by transmission electron microscopy (TEM) and high resolution electron microscopy (HREM). The SiC w/AZ91 interface is very clean in the composites with no binders. For the composites with acid aluminum phosphate binders or silica binders, there exists fine discrete interfacial reaction products MgO at the interface, and a definite orientation relationship between MgO and SiC w. The interfacial reaction products MgO is unevenly distributed at different parts of the composite ingot with silica binder, and mainly distributed to the interface at the side part of the composite cylinder. While in the SiC w/AZ91 composite with acid aluminum phosphate binder, MgO particles are distributed evenly at the interface in almost all the parts of the composite ingot. [
基金the National Key Research and Development Program of China(No.2020YFB1713500)Open Fund of State Key Laboratory of Advanced Refractories(No.SKLAR202210)+1 种基金the Student Research Training Plan of Henan University of Science and Technology(Nos.2021026 and 2021035)the Undergraduate Innovation and Entrepreneurship Training Program of Henan Province(No.S202110464005).
文摘Aqueous zinc(Zn)-ion batteries(AZIBs)are one of the most promising large-scale energy storage devices because of the excellent features of zinc metal anodes,including high theoretical capacity(5,855 mAh·cm^(–3)and 820 mAh·g^(−1)),high safety,and natural abundance.Nevertheless,the large-scale applications of AZIBs are mainly limited by the severe interfacial side reactions of zinc metal anodes,which results in low plating/stripping Coulombic efficiency and poor cycling stability.To address this issue,we report an artificial Ta_(2)O_(5)protective layer on zinc foil(Ta_(2)O_(5)@Zn)for suppressing side reactions during Zn deposition/stripping.The results of density functional theory calculation and experiments indicate that Ta_(2)O_(5)@Zn anode can inhibit the side reactions between the electrolyte and zinc anode through the isolation effect.Benefiting from this advantage,the symmetric cells with Ta_(2)O_(5)@Zn anode delivered an ultralong lifespan of 3,000 h with a low overpotential at 0.25 mA·cm^(−2)for 0.05 mAh·cm^(−2).Furthermore,the full cells consisting of Ta_(2)O_(5)@Zn anode and MnO_(2)or NH_(4)V_(4)O_(10)cathode all present outstanding electrochemical performance,indicating its high reliability in practical applications.This strategy brings new opportunities for the future development of rechargeable AZIBs.
基金supported by the Guangdong Major Project of Basic and Applied Basic Research (2020B0301030006)the National Natural Science Foundation of China (52225101)+2 种基金the Scientific Research Foundation of Chongqing University of Technology (2020ZDZ006)the Science and Technology Research Program of the Chongqing Municipal Education Commission (KJZD-K202201108)the University Innovation Research Group of Chongqing (CXQT20023).
文摘A novel melting infiltration by ultrasonic vibration was investigated and applied to fabricate Ti6Al4V(TC4)lattice structure-reinforced Mg-10Gd-2Y-1Zn-xZr(refer to VW92 hereafter,x=0,0.5 wt%)alloy matrix composites.The edge-to-edge matching model indicates that the well-matching and possible orientation relationships(ORs)between theα-Mg andα-Ti,[10-10]_(α-Mg)//[11-23]_(α-Ti) in(0002)_(α-Mg)//(10-10)_(α-Ti) possesses the smallest misfit of 0.4%(f_(r)),and thus theα-Mg grains can nucleate on the TC4 lattice structure.Interfacial reaction occurred in the TC4/VW92+0.5 wt%Zr composites,and the reaction product was confirmed to be Al_(2)Zr_(3),AlZr_(2) andα-Ti(Zr)particles formed by continuous solution of Zr-Ti.Among the interfacial products,the AlZr_(2) phase is a brittle phase with high-volume fraction,which is not conducive to the load transfer.But generally speaking,theα-Ti(Zr)and theα-Mg tend to form a coherent interface,which is beneficial for improving the interfacial bonding strength of composites.
基金support from the Center for Advanced Surface Engineering, under the National Science Foundation Grant No. OIA-1457888the Arkansas EPSCoR Program, ASSET Ⅲ. X. M+1 种基金the financial support from the University of Arkansas, Fayetteville, AR, USAfunded by the U.S. Department of Energy (DOE), Vehicle Technologies Office。
文摘The commercialization of nickel-rich LiNi_(0.8)Mn_(0.1)Co_(0.1)O_(2)(NMC811) has been hindered by its continuous loss of practical capacity and reduction in average working voltage.To address these issues,surface modification has been well-recognized as an effective strategy.Different from the coatings reported in literature to date,in this work,we for the first time report a sulfide coating,amorphous Li_(2)S via atomic layer deposition (ALD).Our study revealed that the conformal nano-Li_(2)S coating shows exceptional protection over the NMC811 cathodes,accounting for the dramatically boosted capacity retention from~11.6%to~71%and the evidently mitigated voltage reduction from 0.39 to 0.18 V after 500 charge–discharge cycles.In addition,the Li_(2)S coating remarkably improved the rate capability of the NMC811 cathode.Our investigation further revealed that all these beneficial effects of the ALD-deposited nano-Li_(2)S coating lie in the following aspects:(i) maintain the mechanical integrity of the NMC811 electrode:(ii) stabilize the NMC electrode/electrolyte interface:and (iii) suppress the irreversible phase transition of NMC structure.Particularly,this study also has revealed that the nano-Li_(2)S coating has played some unique role not associated with traditional non-sulfide coatings such as oxides.In this regard,we disclosed that the Li_(2)S layer has reacted with the released O_(2) from the NMC lattices,and thereby has dramatically mitigated electrolyte oxidation and electrode corrosion.Thus,this study is significant and has demonstrated that sulfides may be an important class of coating materials to tackle the issues of NMCs and other layered cathodes in lithium batteries.
基金supported by the National Natural Science Foundation of China(Grant no.51932011)。
文摘The development of promising zinc anodes mainly suffers from their low plating/stripping coulombic efficiencies when using aqueous electrolyte,which are mainly associated with the interfacial formation of irreversible by-products.It is urgent to develop technologies that can solve this issue fundamentally.Herein,we report an artificial Sc_(2)O_(3) protective film to construct a new class of interface for Zn anode.The density functional theory simulation and experimental results have proven that the interfacial side reaction was inhibited via a stratified adsorption effect between this artificial layer and Zn anode.Benefiting from this novel structure,the Sc_(2)O_(3)-coated Zn anode can run for more than 100 cycles without short circuit and exhibit low voltage hysteresis,and the coulombic efficiency increases by 1.2%.Importantly,it shows a good application prospect when matched with two of popular manganese-based and vanadium-based cathodes.The excellent electrochemical performance of the Sc_(2)O_(3)-coated Zn anode highlights the importance of rational design of anode materials and demonstrates a good way for developing high-performance Zn anodes with long lifespan and high efficiency.
基金the National Natural Science Foundation of China(Grant No.51471059).
文摘A novel liquid settling method was investigated and applied to fabricate TC4 spherical particle reinforced AZ91 alloy matrix composites.This method was called liquid state settling technique in which TC4 particles would settle down under the force of gravity.High volume fraction(50%)particle reinforced AZ91 composites could be easily obtained via this novel method.This is difficult to achieve for other traditional liquid fabrication methods.In addition,there was a good dispersion of TC4 particles in the AZ91 matrix and no clusters were found,which indicate that this method was feasible.Interfacial reaction occurred and the reaction product was confirmed to be Al2Ti.Three kinds of pre-dispersion technologies were used before the settling process and different interfacial microstructures were found.Theoretical calculation and experimental results both indicated that the interfacial product which was embedded in the matrix strengthened the composites and improved the tensile strength.
基金supported by the National Basic Research Program of China(2013CB933104)the National Natural Science Foundation of China(21525313,21173204,21373192,U1332113)+1 种基金MOE Fundamental Research Funds for the Central Universities(WK2060030017)Collaborative Innovation Center of Suzhou Nano Science and Technology
文摘Au nanostructures were prepared on uniform Cu_2O octahedra and rhombic dodecahedra via the galvanic replacement reaction between HAu Cl4 and Cu2O. The compositions and structures were studied by Scanning Electron Microscope(SEM), Transmission Electron Microscope(TEM), High-Resolution Transmission Electron Microscope(HRTEM), X-Ray Diffraction(XRD), X-Ray Absorption Spectroscopy(XAS), X-ray Photoelectron Spectroscopy(XPS) and in-situ DRIFTS spectroscopy of CO adsorption. Different from the formation of Au–Cu alloys on Cu_2O cubes by the galvanic replacement reaction(Chem Nano Mat 2(2016)861-865), metallic Au particles and positively-charged Au clusters form on Cu_2O octahedra and rhombic dodecahedra at very small Au loadings and only metallic Au particles form at large Au loadings. Metallic Au particles on Cu_2O octahedra and rhombic dodecahedra are more active in catalyzing the liquid phase aerobic oxidation reaction of benzyl alcohol than positively-charged Au clusters. These results demonstrate an obvious morphology effect of Cu_2O nanocrystals on the liquid–solid interfacial reactions and prove oxide morphology as an effective strategy to tune the surface reactivity and catalytic performance.
基金financial support of the National Natural Science Foundation of China(Nos.51731004 and 51671054)the Natural Science Foundation of Jiangsu Province(No.BK20181285)the Fundamental Research Funds for the Central Universities,China(No.2242019K 40056).
文摘Ti_(3)AlC_(2)-reinforced Ag-based composites,which are used as sliding current collectors,electrical contacts,and electrode materials,exhibit remarkable performances.However,the interfacial reactions between Ag and Ti_(3)AlC_(2) significantly degrade the electrical and thermal properties of these composites.To diminish these interfacial reactions,we fabricated carbon-coated Ti_(3)AlC_(2) particles(C@Ti_(3)AlC_(2))as reinforcement and prepared Ag–10wt%C@Ti_(3)AlC_(2) composites with carbon-layer thicknesses ranging from 50–200 nm.Compared with the uncoated Ag–Ti_(3)AlC_(2) composite,Ag–C@Ti_(3)AlC_(2) was found to have a better distribution of Ti_(3)AlC_(2) particles.With increases in the carbon-layer thickness,the Vickers hardness value and relative density of Ag–C@Ti_(3)AlC_(2) gradually decreases.With a carbon-layer thickness of 150 nm,we obtained the lowest resistivity of Ag–C@Ti_(3)AlC_(2) of 29.4135.5×10^(−9)Ω·m,which is half that of Ag–Ti_(3)AlC_(2)(66.7×10^(−9)Ω·m).The thermal conductivity of Ag–C@Ti_(3)AlC_(2) reached a maximum value of 135.5 W·m^(−1)·K^(−1) with a 200-nm carbon coating(~1.8 times that of Ag–Ti_(3)AlC_(2)).These results indicate that the carbon-coating method is a feasible strategy for improving the performance of Ag–C@Ti_(3)AlC_(2) composites.
基金supported by National Nature Science Foundation of China(NSFC22078228)。
文摘Lean electrolyte usage in lithium–sulfur battery(LSB)meets the demand of the high energy density.However,lean condition makes the electrolyte-related interface discrete,leading to retardation of ion transfer that depends on interfaces.Consequently,electrochemical reactions face restraint.Herein,lithium polyacrylate acid(LiPAA)with short-chain anions(molecular weight of 2000)is introduced into the cathode.Because of the polysulfide(PS)-philic instinct of the short-chain PAA anions,short-chain PS is captured inside of the cathode.In addition,LiPAA supplies Li^(+)to the short-chain PS captured.The strong interaction between Li_(2)S_(4)and LiPAA effectively decreases Li_(2)S_(4)migration to the anode during discharging.In a sense,the ion mass transfer pattern is thus changed comparing to traditional long-way mode between cathode and anode.Galvanostatic intermittent titration technique(GITT)proves that the interfacial reaction resistance is greatly decreased in the region where Li_(2)S_(x)(x≤4)reduction contributes most.In the same time,the reversibility of electrochemical reduction/oxidation is improved.Owing to the accelerated Li_(2)S_(x)(x≤4)reduction,Li implanting of only 0.3 wt.%plus O introduction up to 1.4 wt.%enables the LSB perform well even with 1/4 of regular electrolyte dosage(5μL mg^(-1))and high-sulfur loading(4.2 mg cm^(-2)),increasing its rate capacity C_(0.8/0.5)from 52.6%(without the LiPAA)to 92.3%(with the LiP AA)as well as a capacity of 518.7 mAh g^(-1)after 400 cycles at 0.8 mA cm^(-2).
