Ni-rich cathode material is one of the most promising materials for Li-ion batteries in electric vehicles.However,fading capacity,poor cyclic stability and high p H value are still major challenges,which suppress its ...Ni-rich cathode material is one of the most promising materials for Li-ion batteries in electric vehicles.However,fading capacity,poor cyclic stability and high p H value are still major challenges,which suppress its practical application.In this study,spherical LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)powders with 0.4 wt%TiO_(2)coating layer were prepared by impregnation-hydrolysis method.Scanning electron microscopy(SEM),high-resolution transmission electron microscopy(HRTEM)and X-ray diffraction(XRD)results show that TiO_(2)is uniformly coated on the surface of LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)particle and slightly embedded into LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)particles.After 100 cycles at 2.0 C,0.4 wt%TiO_(2)-coated LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode delivers much higher discharge capacity retention(77.0%)than the pristine LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode(63.3%).The excellent cycling performance of 0.4 wt%Ti O_(2)-coated LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode at a high discharge ratio is due to a TiO_(2)coating layer which can effectively reduce the direct contact between cathode material and electrolyte,suppress the oxidation of electrolyte,improve electrical conductivity of the electrode and increase the stability of the structure.展开更多
Lithium sulfur batteries(LSBs)are recognized as promising devices for developing next-generation energy storage systems.In addition,they are attractive rechargeable battery systems for replacing lithium-ion batteries(...Lithium sulfur batteries(LSBs)are recognized as promising devices for developing next-generation energy storage systems.In addition,they are attractive rechargeable battery systems for replacing lithium-ion batteries(LIBs)for commercial use owing to their higher theoretical energy density and lower cost compared to those of LIBs.However,LSBs are still beset with some persistent issues that prevent them from being used industrially,such as the unavoidable dissolution of lithium polysulfide intermediates during electrochemical reactions and large volume expansion(up to 80%)upon the formation of Li_(2)S,resulting in serious battery life and safety limitations.In the process of solving these problems,it is necessary to maintain a high sulfur content in the cathode materials to ensure that the LSBs have high energy densities and excellent cycle performance.In this review,the novel preparation methods and cathode materials used for preparing LSBs in recent years are reviewed considering the sulfur content and cycle performance.In addition,the problems and difficulties in practically applying cathode materials are described,and the development trend is discussed.展开更多
Plasma spray-physical vapor deposition(PS-PVD)as a novel process was used to prepare feather-like columnar thermal barrier coatings(TBCs).This special microstructure shows good strain tolerance and non-line-of-sight(N...Plasma spray-physical vapor deposition(PS-PVD)as a novel process was used to prepare feather-like columnar thermal barrier coatings(TBCs).This special microstructure shows good strain tolerance and non-line-of-sight(NLOS)deposition,giving great potential application in aero-engine.However,due to serious service environment of aero-engine,particle erosion performance is a weakness for PS-PVD 7YSZ TBCs.As a solution,an Al-modification approach was proposed in this investigation.Through in-situ reaction of Al and ZrO2,anα-Al2O3 overlay can be formed on the surface of 7YSZ columnar coating.The results demonstrate that this approach can improve particle erosion resistance since hardness improvement of Al-modified TBCs.Meanwhile,as another important performance of thermal cycle,it has a better optimization with 350-cycle water-quenching,compared with the as-sprayed TBCs.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
The construction of stable cathode electrolyte interphase(CEI)is the key to improve the NCM811 particle structure and interfacial stability via electrolyte engineering.In He’s work,lithium hexamethyldisilazide(LiHMDS...The construction of stable cathode electrolyte interphase(CEI)is the key to improve the NCM811 particle structure and interfacial stability via electrolyte engineering.In He’s work,lithium hexamethyldisilazide(LiHMDS)as the electrolyte additive is proposed to facilitate the generation of stable CEI on NCM811 cathode surface and eliminate H_(2)O and HF in the electrolyte at the same time,which boosts the cycling performance of Li||NCM811 battery up to 1000 or 500 cycles with 4.5 V cut-off voltage at 25 or 60℃.展开更多
This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other...This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other characterization techniques were applied to examine the influence of the ultrasonic power on the sonochemical growth of Y(OH)3 microparticles in direct contact with zinc powder.Electrochemical properties of zinc electrodes containing Y(OH)3 microparticles were discussed through the measurements of potentiodynamic polarization and cyclic voltammetry.Simultaneously,the test cells making use of such modified zinc powder were assembled to further evaluate the availability of Y(OH)3 microparticles in improving the cycle properties of zinc electrodes.It was found that good alkaline environment generated by ultrasonic irradiation of high power led to the formation of Y(OH)3 microparticles on the surface of modified zinc powder due to high-energy jets of immersion solution.In particular,the Y(OH)3 microparticles formed with the ultrasonic power of 440 W made the greatest contributions to hinder the corrosion of zinc electrode and the dissolution of zinc oxidation products in alkaline electrolyte as compared with other power parameters.Besides,the detections of assembled cells at a high discharge current density of 250 mA/cm2 revealed that the Y(OH)3 microparticles obtained with ultrasonic power of 440 W provided the alkaline zinc electrode with low capacity loss and persistent cycle behavior.The great improvement over the corrosion behavior and cycle properties of zinc electrode is possibly ascribed to the uniform distribution of Y(OH)3 microparticles on the surface of modified zinc powder.展开更多
Currently,developing supercapacitors with robust cycle stability and suitability for wide-temperature-range operations is still a huge challenge.In the present work,few-layer hexagonal boron nitride nanosheets(h-BNNSs...Currently,developing supercapacitors with robust cycle stability and suitability for wide-temperature-range operations is still a huge challenge.In the present work,few-layer hexagonal boron nitride nanosheets(h-BNNSs)with a thickness of 2−4 atomic layers were fabricated via vacuum freeze-drying and nitridation.Then,the h-BNNSs/reduced graphene oxide(rGO)composite were further prepared using a hydrothermal method.Due to the combination of two two-dimensional(2D)van der Waals-bonded materials,the as-prepared h-BNNSs/rGO electrode exhibited robustness to wide-temperature-range operations from−10 to 50℃.When the electrodes worked in a neutral aqueous electrolyte(1 M Na2SO4),they showed a great stable cycling performance with almost 107%reservation of the initial capacitance at 0℃ and 111% at 50℃ for 5000 charge−discharge cycles.展开更多
To solve low efficiency,environmental pollution,and toxicity for synthesizing zeolitic imidazolate frameworks(ZIFs)in organic solvents,a KOH-assisted aqueous strategy is proposed to synthesize bimetallic ZIFs polyhedr...To solve low efficiency,environmental pollution,and toxicity for synthesizing zeolitic imidazolate frameworks(ZIFs)in organic solvents,a KOH-assisted aqueous strategy is proposed to synthesize bimetallic ZIFs polyhedrons,which are used as precursors to prepare bimetallic selenide and N-doped carbon(NC)composites.Among them,Fe–Co–Se/NC retains the three-dimensional(3D)polyhedrons with mesoporous structure,and Fe–Co–Se nanoparticles are uniform in size and evenly distributed.When assessed as anode material for lithium-ion batteries,Fe–Co–Se/NC achieves an excellent initial specific capacity of 1165.9 m Ah·g^(-1)at 1.0 A·g^(-1),and the reversible capacity of Fe–Co–Se/NC anode is 1247.4 m Ah·g^(-1)after 550 cycles.It is attributed to that the uniform composite of bimetallic selenides and N-doped carbon can effectively tune redox active sites,the stable 3D structure of Fe–Co–Se/NCs guarantees the structural stability and wettability of the electrolyte,and the uniform distribution of Fe–Co–S nanoparticles in size esuppresses the volume expansion and accelerates the electrochemical reaction kinetics.展开更多
Sodium-ion battery is a potential application system for large-scale energy storage due to the advantage of higher nature abundance and lower production cost of sodium-based materials.However,there exist inevitably th...Sodium-ion battery is a potential application system for large-scale energy storage due to the advantage of higher nature abundance and lower production cost of sodium-based materials.However,there exist inevitably the safety problems such as flammability due to the use of the same type of organic liquid electrolyte with lithium-ion battery.Gel polymer electrolytes are being considered as an effective solution to replace conventional organic liquid electrolytes for building safer sodium-ion batteries.In this review paper,the authors present a comprehensive overview of the research progress in electrochemical and physical properties of the gel polymer electrolyte-based sodium batteries.The gel polymer electrolytes based on different polymer hosts namely poly(ethylene oxide),poly(acrylonitrile),poly(methyl methacrylate),poly(vinylidene fluoride),poly(vinylidene fluoride-hexafluoro propylene),and other new polymer networks are summarized.The ionic conductivity,ion transference number,electrochemical window,thermal stability,mechanical property,and interfacial issue with electrodes of gel polymer electrolytes,and the corresponding influence factors are described in detail.Furthermore,the ion transport pathway and ion conduction mechanism are analyzed and discussed.In addition,the advanced gel polymer electrolyte systems including flame-retardant polymer electrolytes,composite gel polymer electrolytes,copolymerization,single-ion conducting polymer electrolytes,etc.with more superior and functional performance are classified and summarized.Finally,the application prospects,development opportunities,remaining challenges,and possible solutions are discussed.展开更多
Layered oxide is a promising cathode material for sodium-ion batteries because of its high-capacity,high operating voltage,and simple synthesis.Cycling performance is an important criterion for evaluating the applicat...Layered oxide is a promising cathode material for sodium-ion batteries because of its high-capacity,high operating voltage,and simple synthesis.Cycling performance is an important criterion for evaluating the application prospects of batteries.However,facing challenges,including phase transitions,ambient stability,side reactions,and irreversible anionic oxygen activity,the cycling performance of layered oxide cathode materials still cannot meet the application requirements.Therefore,this review proposes several strategies to address these challenges.First,bulk doping is introduced from three aspects:cationic single doping,anionic single doping,and multi-ion doping.Second,homogeneous surface coating and concentration gradient modification are reviewed.In addition,methods such as mixed structure design,particle engineering,high-entropy material construction,and integrated modification are proposed.Finally,a summary and outlook provide a new horizon for developing and modifying layered oxide cathode materials.展开更多
Transition metal oxides have been actively exploited for application in lithium ion batteries due to their facile synthesis,high specific capacity,and environmental-friendly.In this paper,Fe3O4@TiO2@C yolk-shell(Y-S)s...Transition metal oxides have been actively exploited for application in lithium ion batteries due to their facile synthesis,high specific capacity,and environmental-friendly.In this paper,Fe3O4@TiO2@C yolk-shell(Y-S)spheres,used as anode material for lithium ion batteries,were successfully fabricated by Stober method.XRD patterns reveal that Fe3O4@TiO2@C Y-S spheres possess a good crystallinity.But the diffraction peaks’intensity of Fe3O4 crystals in the composites is much weaker than that of bare Fe3O4 spheres,indicating that the outer anatase TiO2@C layer can cover up the diffraction peaks of inner Fe3O4 spheres.The yolk-shell structure of Fe3O4@TiO2@C spheres is further characterized by TEM,HAADFSTEM,and EDS mapping.The yolk-shell structure is good for improving the cycling stability of the inner Fe3O4 spheres during lithium ions insertion-extraction processes.When tested at 200 mA/g,the Fe3O4@TiO2@C Y-S spheres can provide a stable discharge capacity of 450 mAh/g over 100 cycles,which is much better than that of bare Fe3O4 spheres and TiO2@C spheres.Furthermore,cyclic voltammetry curves show that the composites have a good cycling stability compared to bare Fe3O4 spheres.展开更多
The lithium–sulfur batteries show the great potential to be the most promising candidate for high energy applications. However, the shuttling of soluble polysulfides deteriorates the battery performance tremendously....The lithium–sulfur batteries show the great potential to be the most promising candidate for high energy applications. However, the shuttling of soluble polysulfides deteriorates the battery performance tremendously. To suppress the diffusion of soluble polysulfides, diatomite that has abundant natural three-dimensional ordered pores is incorporated into the cathode to trap polysulfides. The composite cathode material(S-DM-AB for short), including sulfur(S), diatomite(DM), and acetylene black(AB) is prepared by an impregnation method. For comparison, another composite cathode material(S-AB for short) including sulfur and acetylene black is also prepared by the same method. The battery with S-DMAB composite cathode material delivers a discharge capacity of 531.4 m Ah/g after 300 cycles at 2 C with a capacity retention of 51.6% at room temperature. By contrast, the battery with S-AB composite cathode material delivered a capacity of only 196.9 m Ah/g with a much lower capacity retention of 18.6% under the same condition. The addition of diatomite in the cathode is proved to be a cheap and effective way to improve the life time of the lithium sulfur batteries.展开更多
Achieving low charge overpotentials represents one of the most critical challenges for pursuing highperformance lithium-oxygen(Li-O_(2))batteries.Herein,we propose a strategy to realize low charge overpotentials by co...Achieving low charge overpotentials represents one of the most critical challenges for pursuing highperformance lithium-oxygen(Li-O_(2))batteries.Herein,we propose a strategy to realize low charge overpotentials by confining the growth of lithium peroxide(Li_(2)O_(2))inside mesoporous channels of cathodes(CMK-8).The CMK-8 cathode with tortuous pore structures can extend the diffusion distance of lithium superoxide(LiO_(2))in the mesoporous channels,facilitating the further reduction of LiO_(2) to lithium peroxide(Li_(2)O_(2))inside the pores and preventing them to be diffused out of the pores.Therefore,Li_(2)O_(2) is trapped in the mesoporous channels of CMK-8 cathodes,ensuring a good Li_(2)O_(2)/CMK-8 contact interface.The CMK-8 electrode exhibits a low charge overpotential of 0.43 V and a good cycle life for 72 cycles with a fixed capacity of 500 m Ah g^(-1) at 0.1 A g^(-1).This study proposes a strategy to achieve a low charge overpotential by confining Li_(2)O_(2) growth in the mesoporous channels of cathodes.展开更多
The effects of cycle potential window on electrochemical behaviors,structural characteristics,and surface changes in Li[Ni_(0.133)Li_(0.2)Co_(0.133)Mn_(0.533)]O_(2)(or 0.5 Li_(2)MnO_(3)·0.5 Li(Co_(0.333)Ni_(0.333...The effects of cycle potential window on electrochemical behaviors,structural characteristics,and surface changes in Li[Ni_(0.133)Li_(0.2)Co_(0.133)Mn_(0.533)]O_(2)(or 0.5 Li_(2)MnO_(3)·0.5 Li(Co_(0.333)Ni_(0.333)Mn_(0.333))O2)in lithium-ion battery were investigated.Two flat charge potential plateaus,~3.9 and~4.5 V,are observed in the initial charge curves of the cells.Sharp changes in specific capacity and columbic efficiency are presented at~4.5 V during the first cycle.XRD specific peaks show an obvious shift with the increase in charge cutoff potential.When the charge cutoff potential is above4.4 V,the cycle performance decreases with the increase in charge cutoff potentials.A film with the composition of C and O elements is observed on the cycled composite particle.展开更多
Aiming at solving the problem of high global warming potential of R134 a,a new mixed refrigerant R13 I1/R152 a(molar fraction ratio of 35:65)with no ozone depletion potential and low global warming potential was propo...Aiming at solving the problem of high global warming potential of R134 a,a new mixed refrigerant R13 I1/R152 a(molar fraction ratio of 35:65)with no ozone depletion potential and low global warming potential was proposed as a substitute for R134 a in automotive air conditioning.The computational models for the thermodynamic properties of R13 I1/R152 a were established by using the PR(Peng-Robinson)equation of state combined with the vdW mixing rule.Based on these models,the cycle performance of this working fluid was calculated,which was also compared with that of R134 a and R1234 yf under the different operating conditions.The results show that R13 I1/R152 a is a near azeotropic refrigerant whose temperature glide is approximately 0,and the saturated vapor pressure curve of which is equivalent to that of R134 a.Moreover,compared to R134 a,R13 I1/R152 a has an average 5.7%improvement in coefficient of performance as well as similar volumetric cooling capacity.The average coefficient of performance and volumetric cooling capacity of R13 I1/R152 a are significantly higher than those of R1234 yf by 13.8%and12.0%,respectively.However,the average discharge temperature of R13 I1/R152 a is approximately13.3 K higher than that of R134 a,but it is also within reasonable limits.Hence,the application of the proposed refrigerant R13 I1/R152 a in automotive air conditioning system is technically feasible.展开更多
Silicon monoxide(SiO)has aroused increased attention as one of the most promising anodes for high-energy density Li-ion batteries.To enhance the initial Coulombic efficiencies(ICE)and cycle stability of SiO-based anod...Silicon monoxide(SiO)has aroused increased attention as one of the most promising anodes for high-energy density Li-ion batteries.To enhance the initial Coulombic efficiencies(ICE)and cycle stability of SiO-based anodes,a new facile composition and electrode design strategy have been adapted to fabricate a SiO-Sn-Co/graphite(G)anode.It achieves a unique structure where tiny milled SiO-Sn-Co particles are dispersed among two graphite layers.In this hybrid electrode,Sn-Co alloys promoted Li;extraction kinetics,and the holistic reversibility of SiO and graphite enhanced the electrical conductivity.The SiO-Sn-Co/G electrode delivered an average ICE of 77.6%and a reversible capacity of 640 mAh g^(-1)at 800 mA g^(-1),and the capacity retention was above 98%after 100 cycles,which was much higher than that of the SiO with an ICE of 55.3%and a capacity retention of 50%.These results indicated that this was reliable method to improve the reversibility and cycle ability of the SiO anode.Furthermore,based on its easy and feasible fabrication process,it may provide a suitable choice to combine other alloy anodes with the graphite anode.展开更多
Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density ...Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density functional theory calcula-tions,the excellent performance of NH_(4)^(+)insertion in Prussian blue analogues(PBAs)is proposed,especially for copper hexacyanoferrate(CuHCF).In this work,we prove the outstanding cycling and rate performance of CuHCF via electrochemical analyses,delivering no capacity fading during ultra-long cycles of 3000 times and high capacity retention of 93.6%at 50 C.One of main contributions to superior performance from highly reversible redox reaction and structural change is verified during the ammoniation/de-ammoniation progresses.More importantly,we propose the NH_(4)^(+)diffusion mechanism in CuHCF based on con-tinuous formation and fracture of hydrogen bonds from a joint theoretical and experimental study,which is another essential reason for rapid charge transfer and superior NH_(4)^(+)storage.Lastly,a full cell by coupling CuHCF cathode and polyaniline anode is constructed to explore the practical application of CuHCF.In brief,the outstanding aqueous NH_(4)^(+)storage in cubic PBAs creates a blueprint for fast and sustainable energy storage.展开更多
The lithium-ion capacitor is a promising energy storage system with a higher energy density than traditional supercapacitors.However,its cycling and rate performances,which depend on the electrochemical properties of ...The lithium-ion capacitor is a promising energy storage system with a higher energy density than traditional supercapacitors.However,its cycling and rate performances,which depend on the electrochemical properties of the anode,are still required to be improved.In this work,soft carbon anodes reinforced using carbon-Si composites of various compositions were fabricated to investigate their beneficial influences on the performance of lithium-ion capacitors.The results showed that the specific capacities of the anodes increased significantly by 16.6 mAh g^(-1) with 1.0 wt% carbon-Si composite,while the initial discharge efficiency barely changed.The specific capacity of the anode with a 10.0 wt% carbon-Si composite reached 513.1 mAh g^(-1),and the initial discharge efficiency was 83.79%.Furthermore,the anodes with 7.5 wt% or lower amounts of carbon-Si composite demonstrated reduced charge transfer resistances,which caused an improvement in the rate performance of the lithium-ion capacitors.Moreover,the use of the optimized amount(7.5 wt%) of carbon-Si composite in the anode could significantly improve the cycling performance of the lithium-ion capacitor by compensating the consumption of active lithium.The capacity retention of the lithium-ion capacitor reached 95.14% at 20 C after 10,000 cycles,while the anode potential remained below 0.412 V,which is much lower than that of a soft carbon anode.展开更多
The shuttle effect of lithium polysulfides(UPSs)in lithium-sulfur batteries(LSBs)has been hampered their commercialization.Metal oxides as separator modifications can suppress the shuttle effect.Since there is no dire...The shuttle effect of lithium polysulfides(UPSs)in lithium-sulfur batteries(LSBs)has been hampered their commercialization.Metal oxides as separator modifications can suppress the shuttle effect.Since there is no direct electron transport between metal oxides and UPSs,absorbed UPSs should be diffused from the surface of metal oxides to the carbon matrix to go through redox reactions.If diffusivity of UPSs from metal oxides surface to carbon substrate is poor,it would hinder the redox reactions of LiPSs.Nevertheless,researchers tend to focus on the adsorption and overlook the diffusion of UPSs.Herein,same morphology and different crystal phase of TiO_(2) nanosheets grown on carbon nanotubes(CNTs@TiO_(2)-bronze and CNTs@TiO_(2)-anatase)have been designed via a simple approach.Compared with CNTs and CNTs@TiO_(2)-anatase composites,the battery with CNTs@TiO_(2)-bronze modified separator delivers higher specific capacities and stronger cycling stability,especially at high current rates(~472 mAh·g^(-1) at 2.0 C after 1,000 cycles).Adsorption tests,density functional theory calculations and electrochemical performance evaluations indicate that suitable diffusion and adsorption for LiPSs on the CNTs@TiO_(2)-B surface can effectively capture LiPSs and promote the redox reaction,leading to the superior cycling performances.展开更多
All-solid-state lithium batteries(ASSLB) are promising candidates for next-generation energy storage devices.Nevertheless,the large-scale commercial application of high energy density AS S LB with the polymer electrol...All-solid-state lithium batteries(ASSLB) are promising candidates for next-generation energy storage devices.Nevertheless,the large-scale commercial application of high energy density AS S LB with the polymer electrolyte still faces challenges.In this study,a thin solid polymer composite electrolyte(SPCE) is prepared through a facile and cost-effective strategy with an infiltration of thermoplastic polyurethane(TPU),lithium salt(LiTFSI or LiFSI),and halloysite nanotubes(HNTs) in a porous framework of polyethylene separator(PE)(TPU-HNTs-LiTFSI-PE or TPU-HNTs-LiFSI-PE).The composition,electrochemical performance,and especially the effect of anions(TFSI-and FSI-) on cycling performance are investigated.The results reveal that the flexible TPU-HNTs-LiTFSI-PE and TPU-HNTs-LiFSI-PE with a thickness of 34 μm exhibit wide electrochemical windows of 4.9 and 5.1 V(vs.Li+/Li) at 60℃,respectively.Reduction in FSI-tends to form more LiF and sulfur compounds at the interface between TPU-HNTs-LiFSI-PE and Li metal anode,thus enhancing the interfacial stability.As a result,cell composed of TPU-HNTs-LiFSI-PE exhibits a smaller increase in interfacial resistance of solid electrolyte interphase(SEI) with a distinct decrease in charge-transfer resistance during cycling.Li|Li symmetric cell with TPU-HNTs-LiFSI-PE could keep its stable overpotential profile for nearly 1300 h with a low hysteresis of approximately39 mV at a current density of 0.1 mA cm-2,while a sudden voltage rise with internal cell impedance-surge signals was observed within 600 h for cell composed of TPU-HNTs-LiTFSI-PE.The initial capacities of NCMITPU-HNTs-LiTFSIPEILi and NCMITPU-HNTs-LiFSI-PEILi cells were 149 and 114 mAh g-1,with capacity retention rates of 83.52% and89.99% after 300 cycles at 0.5 C,respectively.This study provides a valuable guideline for designing flexible SPCE,which shows great application prospect in the practice of ASSLB.展开更多
基金the National Natural Science Foundation of China(No.51701173)。
文摘Ni-rich cathode material is one of the most promising materials for Li-ion batteries in electric vehicles.However,fading capacity,poor cyclic stability and high p H value are still major challenges,which suppress its practical application.In this study,spherical LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)powders with 0.4 wt%TiO_(2)coating layer were prepared by impregnation-hydrolysis method.Scanning electron microscopy(SEM),high-resolution transmission electron microscopy(HRTEM)and X-ray diffraction(XRD)results show that TiO_(2)is uniformly coated on the surface of LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)particle and slightly embedded into LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)particles.After 100 cycles at 2.0 C,0.4 wt%TiO_(2)-coated LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode delivers much higher discharge capacity retention(77.0%)than the pristine LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode(63.3%).The excellent cycling performance of 0.4 wt%Ti O_(2)-coated LiNi_(0.)9Co_(0.08)Al_(0.02)O_(2)electrode at a high discharge ratio is due to a TiO_(2)coating layer which can effectively reduce the direct contact between cathode material and electrolyte,suppress the oxidation of electrolyte,improve electrical conductivity of the electrode and increase the stability of the structure.
基金the National Natural Science Foundation of China(52103093)the Young Elite Scientists Sponsorship Program by China Association for Science and Technology(2021QNRC001)+2 种基金the Jiangxi Provincial Natural Science Foundation(20212BAB214048)Science and Technology Support Project of Shangrao(2020L009,2021J006)Science and Technological Project of Education Department of Jiangxi(GJJ211704)for funding their contributions to this paper。
文摘Lithium sulfur batteries(LSBs)are recognized as promising devices for developing next-generation energy storage systems.In addition,they are attractive rechargeable battery systems for replacing lithium-ion batteries(LIBs)for commercial use owing to their higher theoretical energy density and lower cost compared to those of LIBs.However,LSBs are still beset with some persistent issues that prevent them from being used industrially,such as the unavoidable dissolution of lithium polysulfide intermediates during electrochemical reactions and large volume expansion(up to 80%)upon the formation of Li_(2)S,resulting in serious battery life and safety limitations.In the process of solving these problems,it is necessary to maintain a high sulfur content in the cathode materials to ensure that the LSBs have high energy densities and excellent cycle performance.In this review,the novel preparation methods and cathode materials used for preparing LSBs in recent years are reviewed considering the sulfur content and cycle performance.In addition,the problems and difficulties in practically applying cathode materials are described,and the development trend is discussed.
基金We would like to acknowledge the financial support from the National Natural Science Foundation of China(52172067)Guangdong Province Outstanding Youth Foundation(2021B1515020038)+1 种基金Guangdong Special Support Program(2019BT02C629)Guangdong Academy of Sciences Program(2020GDASYL-20200104030).
文摘Plasma spray-physical vapor deposition(PS-PVD)as a novel process was used to prepare feather-like columnar thermal barrier coatings(TBCs).This special microstructure shows good strain tolerance and non-line-of-sight(NLOS)deposition,giving great potential application in aero-engine.However,due to serious service environment of aero-engine,particle erosion performance is a weakness for PS-PVD 7YSZ TBCs.As a solution,an Al-modification approach was proposed in this investigation.Through in-situ reaction of Al and ZrO2,anα-Al2O3 overlay can be formed on the surface of 7YSZ columnar coating.The results demonstrate that this approach can improve particle erosion resistance since hardness improvement of Al-modified TBCs.Meanwhile,as another important performance of thermal cycle,it has a better optimization with 350-cycle water-quenching,compared with the as-sprayed TBCs.
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 the National Natural Science Foundation of China(Grant No.51971090 and U21A20311)。
文摘The construction of stable cathode electrolyte interphase(CEI)is the key to improve the NCM811 particle structure and interfacial stability via electrolyte engineering.In He’s work,lithium hexamethyldisilazide(LiHMDS)as the electrolyte additive is proposed to facilitate the generation of stable CEI on NCM811 cathode surface and eliminate H_(2)O and HF in the electrolyte at the same time,which boosts the cycling performance of Li||NCM811 battery up to 1000 or 500 cycles with 4.5 V cut-off voltage at 25 or 60℃.
基金supported by the Innovation Foundation of BUAA for Ph. D Graduates Provided by Beihang University in China
文摘This work focused on the zinc powder coated with Y(OH)3 microparticles by means of ultrasonic immersion for performance improvement of zinc electrodes in alkaline battery systems.Scanning electron microscopy and other characterization techniques were applied to examine the influence of the ultrasonic power on the sonochemical growth of Y(OH)3 microparticles in direct contact with zinc powder.Electrochemical properties of zinc electrodes containing Y(OH)3 microparticles were discussed through the measurements of potentiodynamic polarization and cyclic voltammetry.Simultaneously,the test cells making use of such modified zinc powder were assembled to further evaluate the availability of Y(OH)3 microparticles in improving the cycle properties of zinc electrodes.It was found that good alkaline environment generated by ultrasonic irradiation of high power led to the formation of Y(OH)3 microparticles on the surface of modified zinc powder due to high-energy jets of immersion solution.In particular,the Y(OH)3 microparticles formed with the ultrasonic power of 440 W made the greatest contributions to hinder the corrosion of zinc electrode and the dissolution of zinc oxidation products in alkaline electrolyte as compared with other power parameters.Besides,the detections of assembled cells at a high discharge current density of 250 mA/cm2 revealed that the Y(OH)3 microparticles obtained with ultrasonic power of 440 W provided the alkaline zinc electrode with low capacity loss and persistent cycle behavior.The great improvement over the corrosion behavior and cycle properties of zinc electrode is possibly ascribed to the uniform distribution of Y(OH)3 microparticles on the surface of modified zinc powder.
基金financially supported by the National Natural Science Foundation for Excellent Young Scholars of China (No. 51522402)the National Postdoctoral Program for Innovative Talents of China (No. BX20180034)+2 种基金the National Natural Science Foundation of China (No. 51902020)the Fundamental Research Funds for the Central Universities (No. FRF-TP-18-045A1)the China Postdoctoral Science Foundation (No. 2018M641192)
文摘Currently,developing supercapacitors with robust cycle stability and suitability for wide-temperature-range operations is still a huge challenge.In the present work,few-layer hexagonal boron nitride nanosheets(h-BNNSs)with a thickness of 2−4 atomic layers were fabricated via vacuum freeze-drying and nitridation.Then,the h-BNNSs/reduced graphene oxide(rGO)composite were further prepared using a hydrothermal method.Due to the combination of two two-dimensional(2D)van der Waals-bonded materials,the as-prepared h-BNNSs/rGO electrode exhibited robustness to wide-temperature-range operations from−10 to 50℃.When the electrodes worked in a neutral aqueous electrolyte(1 M Na2SO4),they showed a great stable cycling performance with almost 107%reservation of the initial capacitance at 0℃ and 111% at 50℃ for 5000 charge−discharge cycles.
基金financially supported by the National Natural Science Foundation of China(No.52102100)the Natural Science Foundation of Jiangsu Province(No.BK20181469)the Guangdong Basic and Applied Basic Research Foundation,China(No.2020A1515110035)。
文摘To solve low efficiency,environmental pollution,and toxicity for synthesizing zeolitic imidazolate frameworks(ZIFs)in organic solvents,a KOH-assisted aqueous strategy is proposed to synthesize bimetallic ZIFs polyhedrons,which are used as precursors to prepare bimetallic selenide and N-doped carbon(NC)composites.Among them,Fe–Co–Se/NC retains the three-dimensional(3D)polyhedrons with mesoporous structure,and Fe–Co–Se nanoparticles are uniform in size and evenly distributed.When assessed as anode material for lithium-ion batteries,Fe–Co–Se/NC achieves an excellent initial specific capacity of 1165.9 m Ah·g^(-1)at 1.0 A·g^(-1),and the reversible capacity of Fe–Co–Se/NC anode is 1247.4 m Ah·g^(-1)after 550 cycles.It is attributed to that the uniform composite of bimetallic selenides and N-doped carbon can effectively tune redox active sites,the stable 3D structure of Fe–Co–Se/NCs guarantees the structural stability and wettability of the electrolyte,and the uniform distribution of Fe–Co–S nanoparticles in size esuppresses the volume expansion and accelerates the electrochemical reaction kinetics.
基金supported by the National Natural Science Foundation of China(Nos.21771164,U1804129)the Natural Science Foundation of Henan Province(No.222300420525)the Zhongyuan Youth Talent Support Program of Henan Province
文摘Sodium-ion battery is a potential application system for large-scale energy storage due to the advantage of higher nature abundance and lower production cost of sodium-based materials.However,there exist inevitably the safety problems such as flammability due to the use of the same type of organic liquid electrolyte with lithium-ion battery.Gel polymer electrolytes are being considered as an effective solution to replace conventional organic liquid electrolytes for building safer sodium-ion batteries.In this review paper,the authors present a comprehensive overview of the research progress in electrochemical and physical properties of the gel polymer electrolyte-based sodium batteries.The gel polymer electrolytes based on different polymer hosts namely poly(ethylene oxide),poly(acrylonitrile),poly(methyl methacrylate),poly(vinylidene fluoride),poly(vinylidene fluoride-hexafluoro propylene),and other new polymer networks are summarized.The ionic conductivity,ion transference number,electrochemical window,thermal stability,mechanical property,and interfacial issue with electrodes of gel polymer electrolytes,and the corresponding influence factors are described in detail.Furthermore,the ion transport pathway and ion conduction mechanism are analyzed and discussed.In addition,the advanced gel polymer electrolyte systems including flame-retardant polymer electrolytes,composite gel polymer electrolytes,copolymerization,single-ion conducting polymer electrolytes,etc.with more superior and functional performance are classified and summarized.Finally,the application prospects,development opportunities,remaining challenges,and possible solutions are discussed.
基金the Fundamental Research Funds for the Central Universities,China(No.06500177)the National Natural Science Foundation of China Joint Fund Project(No.U1764255)。
文摘Layered oxide is a promising cathode material for sodium-ion batteries because of its high-capacity,high operating voltage,and simple synthesis.Cycling performance is an important criterion for evaluating the application prospects of batteries.However,facing challenges,including phase transitions,ambient stability,side reactions,and irreversible anionic oxygen activity,the cycling performance of layered oxide cathode materials still cannot meet the application requirements.Therefore,this review proposes several strategies to address these challenges.First,bulk doping is introduced from three aspects:cationic single doping,anionic single doping,and multi-ion doping.Second,homogeneous surface coating and concentration gradient modification are reviewed.In addition,methods such as mixed structure design,particle engineering,high-entropy material construction,and integrated modification are proposed.Finally,a summary and outlook provide a new horizon for developing and modifying layered oxide cathode materials.
基金supported by the Tianjin Committee of Science and Technology (No.14JCZDJC32400)Tianjin Science and Technology Innovation Platform Program (No.14TXGCCX00017)
文摘Transition metal oxides have been actively exploited for application in lithium ion batteries due to their facile synthesis,high specific capacity,and environmental-friendly.In this paper,Fe3O4@TiO2@C yolk-shell(Y-S)spheres,used as anode material for lithium ion batteries,were successfully fabricated by Stober method.XRD patterns reveal that Fe3O4@TiO2@C Y-S spheres possess a good crystallinity.But the diffraction peaks’intensity of Fe3O4 crystals in the composites is much weaker than that of bare Fe3O4 spheres,indicating that the outer anatase TiO2@C layer can cover up the diffraction peaks of inner Fe3O4 spheres.The yolk-shell structure of Fe3O4@TiO2@C spheres is further characterized by TEM,HAADFSTEM,and EDS mapping.The yolk-shell structure is good for improving the cycling stability of the inner Fe3O4 spheres during lithium ions insertion-extraction processes.When tested at 200 mA/g,the Fe3O4@TiO2@C Y-S spheres can provide a stable discharge capacity of 450 mAh/g over 100 cycles,which is much better than that of bare Fe3O4 spheres and TiO2@C spheres.Furthermore,cyclic voltammetry curves show that the composites have a good cycling stability compared to bare Fe3O4 spheres.
基金support from the National Natural Science Foundation of China(nos.21403202,21233006 and 21473164)the Key Program of the Natural Science Foundation of Hubei Province(no.2015CFA129)+1 种基金the Undergraduate Innovation Training Program of CUG(no.201610491138)the Excellent Youth of CUG Scholars
文摘The lithium–sulfur batteries show the great potential to be the most promising candidate for high energy applications. However, the shuttling of soluble polysulfides deteriorates the battery performance tremendously. To suppress the diffusion of soluble polysulfides, diatomite that has abundant natural three-dimensional ordered pores is incorporated into the cathode to trap polysulfides. The composite cathode material(S-DM-AB for short), including sulfur(S), diatomite(DM), and acetylene black(AB) is prepared by an impregnation method. For comparison, another composite cathode material(S-AB for short) including sulfur and acetylene black is also prepared by the same method. The battery with S-DMAB composite cathode material delivers a discharge capacity of 531.4 m Ah/g after 300 cycles at 2 C with a capacity retention of 51.6% at room temperature. By contrast, the battery with S-AB composite cathode material delivered a capacity of only 196.9 m Ah/g with a much lower capacity retention of 18.6% under the same condition. The addition of diatomite in the cathode is proved to be a cheap and effective way to improve the life time of the lithium sulfur batteries.
基金the financial support from the National Natural Science Foundation of China(91645102)the Singapore MOE grant(R143-000-A29-112)the Hundred Talents Sailing Project of Jiangxi province,China。
文摘Achieving low charge overpotentials represents one of the most critical challenges for pursuing highperformance lithium-oxygen(Li-O_(2))batteries.Herein,we propose a strategy to realize low charge overpotentials by confining the growth of lithium peroxide(Li_(2)O_(2))inside mesoporous channels of cathodes(CMK-8).The CMK-8 cathode with tortuous pore structures can extend the diffusion distance of lithium superoxide(LiO_(2))in the mesoporous channels,facilitating the further reduction of LiO_(2) to lithium peroxide(Li_(2)O_(2))inside the pores and preventing them to be diffused out of the pores.Therefore,Li_(2)O_(2) is trapped in the mesoporous channels of CMK-8 cathodes,ensuring a good Li_(2)O_(2)/CMK-8 contact interface.The CMK-8 electrode exhibits a low charge overpotential of 0.43 V and a good cycle life for 72 cycles with a fixed capacity of 500 m Ah g^(-1) at 0.1 A g^(-1).This study proposes a strategy to achieve a low charge overpotential by confining Li_(2)O_(2) growth in the mesoporous channels of cathodes.
基金financially supported by the HiTech Research and Development Program of China (No. 2011AA11A254)
文摘The effects of cycle potential window on electrochemical behaviors,structural characteristics,and surface changes in Li[Ni_(0.133)Li_(0.2)Co_(0.133)Mn_(0.533)]O_(2)(or 0.5 Li_(2)MnO_(3)·0.5 Li(Co_(0.333)Ni_(0.333)Mn_(0.333))O2)in lithium-ion battery were investigated.Two flat charge potential plateaus,~3.9 and~4.5 V,are observed in the initial charge curves of the cells.Sharp changes in specific capacity and columbic efficiency are presented at~4.5 V during the first cycle.XRD specific peaks show an obvious shift with the increase in charge cutoff potential.When the charge cutoff potential is above4.4 V,the cycle performance decreases with the increase in charge cutoff potentials.A film with the composition of C and O elements is observed on the cycled composite particle.
基金supported by the National Natural Science Foundation of China(22068024)。
文摘Aiming at solving the problem of high global warming potential of R134 a,a new mixed refrigerant R13 I1/R152 a(molar fraction ratio of 35:65)with no ozone depletion potential and low global warming potential was proposed as a substitute for R134 a in automotive air conditioning.The computational models for the thermodynamic properties of R13 I1/R152 a were established by using the PR(Peng-Robinson)equation of state combined with the vdW mixing rule.Based on these models,the cycle performance of this working fluid was calculated,which was also compared with that of R134 a and R1234 yf under the different operating conditions.The results show that R13 I1/R152 a is a near azeotropic refrigerant whose temperature glide is approximately 0,and the saturated vapor pressure curve of which is equivalent to that of R134 a.Moreover,compared to R134 a,R13 I1/R152 a has an average 5.7%improvement in coefficient of performance as well as similar volumetric cooling capacity.The average coefficient of performance and volumetric cooling capacity of R13 I1/R152 a are significantly higher than those of R1234 yf by 13.8%and12.0%,respectively.However,the average discharge temperature of R13 I1/R152 a is approximately13.3 K higher than that of R134 a,but it is also within reasonable limits.Hence,the application of the proposed refrigerant R13 I1/R152 a in automotive air conditioning system is technically feasible.
基金supported by the National Natural Science Foundation of China (No. 52071144, 51822104, 51831009, and 51621001)
文摘Silicon monoxide(SiO)has aroused increased attention as one of the most promising anodes for high-energy density Li-ion batteries.To enhance the initial Coulombic efficiencies(ICE)and cycle stability of SiO-based anodes,a new facile composition and electrode design strategy have been adapted to fabricate a SiO-Sn-Co/graphite(G)anode.It achieves a unique structure where tiny milled SiO-Sn-Co particles are dispersed among two graphite layers.In this hybrid electrode,Sn-Co alloys promoted Li;extraction kinetics,and the holistic reversibility of SiO and graphite enhanced the electrical conductivity.The SiO-Sn-Co/G electrode delivered an average ICE of 77.6%and a reversible capacity of 640 mAh g^(-1)at 800 mA g^(-1),and the capacity retention was above 98%after 100 cycles,which was much higher than that of the SiO with an ICE of 55.3%and a capacity retention of 50%.These results indicated that this was reliable method to improve the reversibility and cycle ability of the SiO anode.Furthermore,based on its easy and feasible fabrication process,it may provide a suitable choice to combine other alloy anodes with the graphite anode.
基金This work is sponsored by NSAF joint Fund(U1830106)Science and Technology Innovation 2025 Major Program of Ningbo(2018B10061)National Natural Science Foundation of China(U1632114,51901205),and K.C.Wong Magna Fund in Ningbo University.
文摘Aqueous ammonium ion batteries are regarded as eco-friendly and sustainable energy storage systems.And applicable host for NH_(4)^(+)in aqueous solution is always in the process of development.On the basis of density functional theory calcula-tions,the excellent performance of NH_(4)^(+)insertion in Prussian blue analogues(PBAs)is proposed,especially for copper hexacyanoferrate(CuHCF).In this work,we prove the outstanding cycling and rate performance of CuHCF via electrochemical analyses,delivering no capacity fading during ultra-long cycles of 3000 times and high capacity retention of 93.6%at 50 C.One of main contributions to superior performance from highly reversible redox reaction and structural change is verified during the ammoniation/de-ammoniation progresses.More importantly,we propose the NH_(4)^(+)diffusion mechanism in CuHCF based on con-tinuous formation and fracture of hydrogen bonds from a joint theoretical and experimental study,which is another essential reason for rapid charge transfer and superior NH_(4)^(+)storage.Lastly,a full cell by coupling CuHCF cathode and polyaniline anode is constructed to explore the practical application of CuHCF.In brief,the outstanding aqueous NH_(4)^(+)storage in cubic PBAs creates a blueprint for fast and sustainable energy storage.
基金financially supported by the National Natural Science Foundation of China (No.51721005)the Beijing Municipal Science and Technology Commission (No.Z171100000917007)
文摘The lithium-ion capacitor is a promising energy storage system with a higher energy density than traditional supercapacitors.However,its cycling and rate performances,which depend on the electrochemical properties of the anode,are still required to be improved.In this work,soft carbon anodes reinforced using carbon-Si composites of various compositions were fabricated to investigate their beneficial influences on the performance of lithium-ion capacitors.The results showed that the specific capacities of the anodes increased significantly by 16.6 mAh g^(-1) with 1.0 wt% carbon-Si composite,while the initial discharge efficiency barely changed.The specific capacity of the anode with a 10.0 wt% carbon-Si composite reached 513.1 mAh g^(-1),and the initial discharge efficiency was 83.79%.Furthermore,the anodes with 7.5 wt% or lower amounts of carbon-Si composite demonstrated reduced charge transfer resistances,which caused an improvement in the rate performance of the lithium-ion capacitors.Moreover,the use of the optimized amount(7.5 wt%) of carbon-Si composite in the anode could significantly improve the cycling performance of the lithium-ion capacitor by compensating the consumption of active lithium.The capacity retention of the lithium-ion capacitor reached 95.14% at 20 C after 10,000 cycles,while the anode potential remained below 0.412 V,which is much lower than that of a soft carbon anode.
基金supported by funding from the National Natural Science Foundation of China(NSFC)(No.51702236)Tianjin Municipal Science and Technology Commission(No.17JCZDJC38000).
文摘The shuttle effect of lithium polysulfides(UPSs)in lithium-sulfur batteries(LSBs)has been hampered their commercialization.Metal oxides as separator modifications can suppress the shuttle effect.Since there is no direct electron transport between metal oxides and UPSs,absorbed UPSs should be diffused from the surface of metal oxides to the carbon matrix to go through redox reactions.If diffusivity of UPSs from metal oxides surface to carbon substrate is poor,it would hinder the redox reactions of LiPSs.Nevertheless,researchers tend to focus on the adsorption and overlook the diffusion of UPSs.Herein,same morphology and different crystal phase of TiO_(2) nanosheets grown on carbon nanotubes(CNTs@TiO_(2)-bronze and CNTs@TiO_(2)-anatase)have been designed via a simple approach.Compared with CNTs and CNTs@TiO_(2)-anatase composites,the battery with CNTs@TiO_(2)-bronze modified separator delivers higher specific capacities and stronger cycling stability,especially at high current rates(~472 mAh·g^(-1) at 2.0 C after 1,000 cycles).Adsorption tests,density functional theory calculations and electrochemical performance evaluations indicate that suitable diffusion and adsorption for LiPSs on the CNTs@TiO_(2)-B surface can effectively capture LiPSs and promote the redox reaction,leading to the superior cycling performances.
基金financially supported by the National Natural Science Foundation of China(No.21673051)the Department of Science and Technology of Guangdong Province,China(No.2019A050510043)。
文摘All-solid-state lithium batteries(ASSLB) are promising candidates for next-generation energy storage devices.Nevertheless,the large-scale commercial application of high energy density AS S LB with the polymer electrolyte still faces challenges.In this study,a thin solid polymer composite electrolyte(SPCE) is prepared through a facile and cost-effective strategy with an infiltration of thermoplastic polyurethane(TPU),lithium salt(LiTFSI or LiFSI),and halloysite nanotubes(HNTs) in a porous framework of polyethylene separator(PE)(TPU-HNTs-LiTFSI-PE or TPU-HNTs-LiFSI-PE).The composition,electrochemical performance,and especially the effect of anions(TFSI-and FSI-) on cycling performance are investigated.The results reveal that the flexible TPU-HNTs-LiTFSI-PE and TPU-HNTs-LiFSI-PE with a thickness of 34 μm exhibit wide electrochemical windows of 4.9 and 5.1 V(vs.Li+/Li) at 60℃,respectively.Reduction in FSI-tends to form more LiF and sulfur compounds at the interface between TPU-HNTs-LiFSI-PE and Li metal anode,thus enhancing the interfacial stability.As a result,cell composed of TPU-HNTs-LiFSI-PE exhibits a smaller increase in interfacial resistance of solid electrolyte interphase(SEI) with a distinct decrease in charge-transfer resistance during cycling.Li|Li symmetric cell with TPU-HNTs-LiFSI-PE could keep its stable overpotential profile for nearly 1300 h with a low hysteresis of approximately39 mV at a current density of 0.1 mA cm-2,while a sudden voltage rise with internal cell impedance-surge signals was observed within 600 h for cell composed of TPU-HNTs-LiTFSI-PE.The initial capacities of NCMITPU-HNTs-LiTFSIPEILi and NCMITPU-HNTs-LiFSI-PEILi cells were 149 and 114 mAh g-1,with capacity retention rates of 83.52% and89.99% after 300 cycles at 0.5 C,respectively.This study provides a valuable guideline for designing flexible SPCE,which shows great application prospect in the practice of ASSLB.
