Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials ...Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials for SIBs are mainly used as cathodes because of their relatively high redox potentials(>1 V).Organic electrodes with low redox potential that can be used as anode are rare.Herein,a novel organic anode material (tetrasodium 1,4,5,8-naphthalenetetracarboxylate,Na_(4)TDC) has been developed with low redox potential (<0.7 V) and excellent cyclic stability.Its three-sodium storage mechanism was demonstrated with various in-situ/ex-situ spectroscopy and theoretical calculations,showing a high capacity of 208 mAh/g and an average decay rate of merely 0.022%per cycle.Moreover,the Na_(4)TDC-hard carbon composite can further acquire improved capacity and cycling stability for 1200 cycles even with a high mass loading of up to 20 mg cm^(-2).By pairing with a thick Na_(3)V_(2)(PO_(4))_(3)cathode (20.6 mg cm^(-2)),the as-fabricated full cell exhibited high operating voltage (2.8 V),excellent rate performance and cycling stability with a high capacity retention of 88.7% after 200 cycles,well highlighting the Na_(4)TDC anode material for SIBs.展开更多
Carbon materials are widely recognized as highly promising electrode materials for various energy storage system applications.Coal tar residues(CTR),as a type of carbon-rich solid waste with high value-added utilizati...Carbon materials are widely recognized as highly promising electrode materials for various energy storage system applications.Coal tar residues(CTR),as a type of carbon-rich solid waste with high value-added utilization,are crucially important for the development of a more sustainable world.In this study,we employed a straightforward direct carbonization method within the temperature range of 700-1000℃to convert the worthless solid waste CTR into economically valuable carbon materials as anodes for potassium-ion batteries(PIBs).The effect of carbonization temperature on the microstructure and the potassium ions storage properties of CTR-derived carbons(CTRCs)were systematically explored by structural and morphological characterization,alongside electrochemical performances assessment.Based on the co-regulation between the turbine layers,crystal structure,pore structure,functional groups,and electrical conductivity of CTR-derived carbon carbonized at 900℃(CTRC-900H),the electrode material with high reversible capacity of 265.6m Ah·g^(-1)at 50 m A·g^(-1),a desirable cycling stability with 93.8%capacity retention even after 100 cycles,and the remarkable rate performance for PIBs were obtained.Furthermore,cyclic voltammetry(CV)at different scan rates and galvanostatic intermittent titration technique(GITT)have been employed to explore the potassium ions storage mechanism and electrochemical kinetics of CTRCs.Results indicate that the electrode behavior is predominantly governed by surface-induced capacitive processes,particularly under high current densities,with the potassium storage mechanism characterized by an“adsorption-weak intercalation”mechanism.This work highlights the potential of CTR-based carbon as a promising electrode material category suitable for high-performance PIBs electrodes,while also provides valuable insights into the new avenues for the high value-added utilization of CTR.展开更多
Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein...Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein,we comprehensively review recent advancements in the design and development of carbon-based anode materials for PIBs anodes,covering graphite,hard carbon,alloy and conversion materials with carbon,and carbon host for K metal deposition.Chemical strategies such as structural engineering,heteroatom-doping,and surface modifications are highlighted to improve electrochemical performances as well as to resolve technical challenges,such as electrode instability,low initial Coulombic efficiency,and electrolyte compatibility.Furthermore,we discuss the fundamental understanding of potassium-ion storage mechanisms of carbon-based materials and their correlation with electrochemical performance.Finally,we present the current challenges and future research directions for the practical implementation of carbon-based anodes to enhance their potential as next-generation energy storage materials for PIBs.This review aims to provide our own insights into innovative design strategies for advanced PIB's anode through the chemical and engineering strategies.展开更多
The discovery of novel materials with compelling properties is more accessible with the help of advanced computational algorithms.Recent experimental synthesis of the biphenylene network(C_(6))motivated us to discover...The discovery of novel materials with compelling properties is more accessible with the help of advanced computational algorithms.Recent experimental synthesis of the biphenylene network(C_(6))motivated us to discover new BN-doped biphenylene networks(C_(4)BN,C_(2)B_(2)N_(2),and B_(4)N_(4))and their applications in Li(K)-ion batteries using an evolutionary algorithm and the first-principles calculations.The thermodynamic,thermal,and mechanical stability calculations and decomposition energy suggest the experimental synthesis of predicted biphenylene networks.Adding BN in the biphenylene networks shows a transition from metal to semimetal to semiconductor.The BN biphenylene network shows an HSE06 band gap of 3.06 eV,smaller than h-BN.The C_(4)BN and C_(2)B_(2)N_(2)biphenylene networks offer Li(K)adsorption energy of-0.56 eV(-0.81 eV)and-0.14 eV(-0.28 eV),respectively,with a low diffusion barrier of 178 meV(58 meV)and 251 meV(79 meV),and a large diffusion constant of 8.50×10^(-5)cm^(2)=s(8.78×10^(-3)cm^(2)=s)and 5.33×10^(-6)cm^(2)=s(4.12×10^(-3)cm^(2)=s),respectively.The calculated Li(K)theoretical capacity of C_(4)BN and C_(2)B_(2)N_(2)biphenylene networks is 940.21 mA h g^(-1)(899.01 mA h g^(-1))and 768.08 mA h g^(-1)(808.47 mA h g^(-1)),with a low open circuit voltage of 0.34 V(0.23 V),and 0.17 V(0.13 V),resulting in very high energy density of 2576.18 mW h g^(-1)(2445.31 mW h g^(-1))and 2181.35 mW h g^(-1)(2263.72 mW h g^(-1)),respectively.Only a slight volume change of 1.6%confirms the robustness of BN-doped carbon-based biphenylene networks.Our findings present novel 2D BN-doped biphenylene networks and a pathway toward their applications in metal-ion batteries.展开更多
Conjugated microporous polymers(CMPs)have attracted considerable attention as potential organic anode materials for sodium-ion batteries(SIBs)due to their flexible chemical structure,high porosity,environmental friend...Conjugated microporous polymers(CMPs)have attracted considerable attention as potential organic anode materials for sodium-ion batteries(SIBs)due to their flexible chemical structure,high porosity,environmental friendliness,and cost effectiveness.However,the inherent shortcomings of organic electrodes,such as low conductivity,high solubility in electrolyte,narrow material utilization,etc.,limit their further development.In this work,we successfully prepared a novel porous polyimide PPD containing multicarbonyl active centers via the polycondensation of pyromellitic dianhydride(PMDA)and2,6-diaminoanthraquinone(DAAQ).The stable conjugated structure and multiple redox centers give the polymer high reversible specific capacity(244.6 m Ah/g after 100 cycles at 100 m A/g),ultra-long cycle stability(100.7 m Ah/g after 2000 cycles at 1.0 A/g),and predominant rate capability.Meanwhile,the sodium storage mechanism of the electrode materials during the charging and discharging process is investigated by ex-situ XPS/FTIR analysis.Due to the exceptional electrochemical properties and simple synthesis method,this work may shed light on the preparation of polyimide-based anodes for high specific capacity and rate capability secondary batteries.展开更多
Conversion-alloying anode materials are competitive candidates for high-energy-density sodium-ion batteries(SIBs).However,the sluggish dynamics and severe volume expansion during Na insertion/extraction become the key...Conversion-alloying anode materials are competitive candidates for high-energy-density sodium-ion batteries(SIBs).However,the sluggish dynamics and severe volume expansion during Na insertion/extraction become the key bottlenecks hindering their application in SIBs.Herein,SnTe nanoparticles are anchored on reduced graphene oxide(rGO)and encapsulated by nitrogen-doped carbon(NC)to construct SnTe@rGO@NC composite as anode for SIBs,where hierarchical confinement effect can provide a buffer area to accommodate huge volume expansion as well as enhance electronic conductivity and Na-ion transfer kinetics behavior,confirmed by density functional theory(DFT)calculation and experimental study.Meanwhile,structural stability and interfacial charge transfer of the composite can be further improved by the strong chemical bonds of C-Sn and C-Te.High-angle annular dark field scanning transmission electron microscopy visually at atomic scale declares that SnTe@rGO@NC proceeds conversion-alloying dual-mechanism for Na-ion storage employing Sn as redox center(4SnTe+23Na^(+)+23e^(-)→Na_(15)Sn_(4)+4Na_(2)Te).Thus,SnTe@rGO@NC architecture displays a high reversible specific capacity of 261.5 mAh·g^(-1)at 50 mA·g^(-1),superior rate capability and excellent cycling stability with long-term lifespan over 1000 cycles at 200 mA·g^(-1).The multi-physicochemical encapsulation strategy sheds light on the development of a high-performance conversion-alloying anode for SIBs.展开更多
Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the futur...Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the future development of PIBs.Bismuth-based anode materials demonstrate great potential for storing potassium ions(K^(+))due to their layered structure,high theoretical capacity based on the alloying reaction mechanism,and safe operating voltage.However,the large radius of K^(+)inevitably induces severe volume expansion in depotassiation/potassiation,and the sluggish kinetics of K^(+)insertion/extraction limits its further development.Herein,we summarize the strategies used to improve the potassium storage properties of various types of materials and introduce recent advances in the design and fabrication of favorable structural features of bismuth-based materials.Firstly,this review analyzes the structure,working mechanism and advantages and disadvantages of various types of materials for potassium storage.Then,based on this,the manuscript focuses on summarizing modification strategies including structural and morphological design,compositing with other materials,and electrolyte optimization,and elucidating the advantages of various modifications in enhancing the potassium storage performance.Finally,we outline the current challenges of bismuth-based materials in PIBs and put forward some prospects to be verified.展开更多
The urgent demand for clean energy solutions has intensified the search for advanced storage materials,with rechargeable alkali-ion batteries(AIBs)playing a pivotal role in electrochemical energy storage.Enhancing ele...The urgent demand for clean energy solutions has intensified the search for advanced storage materials,with rechargeable alkali-ion batteries(AIBs)playing a pivotal role in electrochemical energy storage.Enhancing electrode performance is critical to addressing the increasing need for high-energy and high-power AIBs.Next-generation anode materials face significant challenges,including limited energy storage capacities and complex reaction mechanisms that complicate structural modeling.Sn-based materials have emerged as promising candidates for AIBs due to their inherent advantages.Recent research has increasingly focused on the development of heterojunctions as a strategy to enhance the performance of Sn-based anode materials.Despite significant advances in this field,comprehensive reviews summarizing the latest developments are still sparse.This review provides a detailed overview of recent progress in Sn-based heterojunction-type anode materials.It begins with an explanation of the concept of heterojunctions,including their fabrication,characterization,and classification.Cutting-edge research on Sn-based heterojunction-type anodes for AIBs is highlighted.Finally,the review summarizes the latest advancements in heterojunction technology and discusses future directions for research and development in this area.展开更多
The scarcity and high cost of lithium resources drive the search for sustainable alternatives,positioning potassium-ion batteries(KIBs)as promising energy storage solutions due to the natural abundance and advantageou...The scarcity and high cost of lithium resources drive the search for sustainable alternatives,positioning potassium-ion batteries(KIBs)as promising energy storage solutions due to the natural abundance and advantageous electrochemical properties of the potassium.This study investigates the enhancement of KIB anodes through phase transformation and electronic structure engineering of monolayer 1T-MoS_(2),achieved via doping with highly electronegative non-metal elements:carbon(C),nitrogen(N),oxygen(O),and fluorine(F).Density functional theory(DFT)simulations reveal that electronegative atom doping enhances phase stability,structural robustness,and thermal resilience,which are key properties for highperformance KIB anodes.Among the doped configurations,F and N-doped 1T-MoS_(2)(MoS_(2-)F and MoS_(2)-N)exhibit superior electrochemical performance,showing optimal adsorption energies and significantly improved electronic conductivity,attributable to favorable charge redistribution and increased active potassium adsorption sites.Specifically,MoS_(2)-F and MoS_(2)-N achieve the highest specific capacities of339.65 and 339.17 mAh/g,respectively,while maintaining stability within an ideal open circuit voltage range,outperforming undoped MoS_(2).This work undersco res the potential of electronegative atom doping in 1T-MoS_(2)to enable sustainable,high-capacity energy storage solutions,offering key advancements in the electrochemical and structural properties of KIB anodes.展开更多
Lithium metal is one of the most promising anodes for lithium batteries because of their high theoretical specific capacity and the low electrochemical potential.However,the commercialization of lithium metal anodes(L...Lithium metal is one of the most promising anodes for lithium batteries because of their high theoretical specific capacity and the low electrochemical potential.However,the commercialization of lithium metal anodes(LMAs)is facing significant obstacles,such as uncontrolled lithium dendrite growth and unstable solid electrolyte interface,leading to inferior Coulombic efficiency,unsatisfactory cycling stability and even serious safety issues.Introducing low-cost natural clay-based materials(NCBMs)in LMAs is deemed as one of the most effective methods to solve aforementioned issues.These NCBMs have received considerable attention for stabilizing LMAs due to their unique structure,large specific surface areas,abundant surface groups,high mechanical strength,excellent thermal stability,and environmental friendliness.Considering the rapidly growing research enthusiasm for this topic in the last several years,here,we review the recent progress on the application of NCBMs in stable and dendrite-free LMAs.The different structures and modification methods of natural clays are first summarized.In addition,the relationship between their modification methods and nano/microstructures,as well as their impact on the electrochemical properties of LMAs are systematically discussed.Finally,the current challenges and opportunities for application of NCBMs in stable LMAs are also proposed to facilitate their further development.展开更多
Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of pota...Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of potassium ions,most conventional anode materials undergo severe volume expansion,making it difficult to achieve stable and reversible energy storage.Therefore,developing high-performance anode materials is one of the critical factors in developing PIBs.In this sense,antimony(Sb)-based anode materials with high theoretical capacity and safe reaction potentials have a broad potential for application in PIBs.However,overcoming the rapid capacity decay induced by the large radius of potassium ions is still an issue that needs to be focused on.This paper reviews the latest research on different types of Sb-based anode materials and provides an in-depth analysis of their optimization strategies.We focus on material selection,structural design,and storage mechanisms to develop a detailed description of the material.In addition,the current challenges still faced by Sb-based anode materials are summarized,and some further optimization strategies have been added.We hope to provide some insights for researchers developing Sb-based anode materials for next-generation advanced PIBs.展开更多
High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanopartic...High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanoparticles serve as catalytic agents,significantly enhancing conductivity,shortening diffusion paths,and accelerating reaction kinetics.Simultaneously,the sulfurized polyacrylonitrile fibers form a three-dimensional matrix that not only provides a continuous network for rapid electron transfer but also prevents zinc sulfide nanoparticle aggregation and mitigates volume changes during charge-discharge cycles.Moreover,the heterointerface structure at the junction of zinc sulfide nanoparticles and the sulfurized polyacrylonitrile matrix increases the availability of active sites and facilitates both ion adsorption and electron transfer.As an anode material for lithium-ion batteries,the zinc sulfide/sulfurized polyacrylonitrile hybrid demonstrates a high reversible capacity of 1178 mAh g^(-1)after 100 cycles at a current density of 0.2 A g^(-1),maintaining a capacity of 788 mAh g^(-1)after 200 cycles at 1 A g^(-1).It also exhibits excellent sodium storage capabilities,retaining a capacity of 625 mAh g^(-1)after 150 cycles at 0.2 A g^(-1).Furthermore,ex-situ X-ray photoelectron spectroscopy,X-ray diffraction,7Li solid-state magic angle spinning nuclear magnetic resonance,and in situ Raman are employed to investigate the reaction mechanisms of the zinc sulfide/sulfurized polyacrylonitrile hybrid anode,providing valuable insights that pave the way for the advancement of hybrid anode materials in lithium-ion batteries and sodium-ion batteries.展开更多
Tin dioxide(SnO_(2))with a high theoretical specific capacity of 1494 mAh g^(-1)is a promising candidate anode material for lithium storage.However,the shortcomings of serious volume expansion and low conductivity lim...Tin dioxide(SnO_(2))with a high theoretical specific capacity of 1494 mAh g^(-1)is a promising candidate anode material for lithium storage.However,the shortcomings of serious volume expansion and low conductivity limit its wide application.Herein,coaxial nano-multilayered C/SnO_(2)/TiO_(2)composites were fabricated via layerby-layer self-assembly of TiO_(2)and SnO_(2)-gel layers on the natural cellulose filter paper,followed by thermal treatment under a nitrogen atmosphere.Through engineering design of the assembly process,the optimal C/SinO_(2)/TiO_(2)composite features five alternating SnO_(2)and TiO_(2)nanolayers,with TiO_(2)as the outside shell(denoted as C/TSTST).This unique structure endows the C/TSTST with excellent structural stability and electrochemical kinetics,making it a high-performance anode for lithium-ion batteries(LIBs).The C/TSTST composite delivers a high reversible capacity of 676 mAh g^(-1)at 0.1 A g^(-1)after 200 cycles and retains a capacity of 504 mAh g^(-1)at 1.0 A g^(-1),which can be recovered to 781 mAh g^(-1)at 0.1 A g^(-1)The significantly enhanced electrochemical performance is attributed to the hierarchical hybrid structure,where the carbon core combined with coaxial TiO_(2)nanolayers serves as a structural scaffold,ameliorating volume change of SnO_(2)while creating abundant interfacial defects for enhanced lithium storage and rapid charge transport.These findings are further demonstrated by the density functional theory(DFT)calculations.This work provides an efficient strategy for designing coaxial nano-multilayered transition metal oxide-related electrode materials,offering new insights into high-performance LIBs anodes.展开更多
A facile way was used to synthesize Cu2O/reduced graphene oxide （rGO） composites with octahedron-like morphology in aqueous solution without any surfactant. TEM images of the obtained Cu2O/rGOs reveal that the Cu2O ...A facile way was used to synthesize Cu2O/reduced graphene oxide （rGO） composites with octahedron-like morphology in aqueous solution without any surfactant. TEM images of the obtained Cu2O/rGOs reveal that the Cu2O particles and rGO distribute hierarchically and the primary Cu2O particles are encapsulated well in the graphene nanosheets. The electrochemical performance of Cu2O/rGOs is enhanced compared with bare Cu2O when they are employed as anode materials for lithium ion batteries. The Cu2O/rGO composites maintain a reversible capacity of 348.4 mA？h/g after 50 cycles at a current density of 100 mA/g. In addition, the composites retain 305.8 mA？h/g after 60 cycles at various current densities of 50, 100, 200, 400 and 800 mA/g.展开更多
The electrochemical performance of Ta-doped Li4Ti5O12 in the form of Li4Ti4.95Ta0.05O12 was characterized.X-ray diffraction（XRD） and scanning electron microscopy（SEM） were employed to characterize the structure an...The electrochemical performance of Ta-doped Li4Ti5O12 in the form of Li4Ti4.95Ta0.05O12 was characterized.X-ray diffraction（XRD） and scanning electron microscopy（SEM） were employed to characterize the structure and morphology of Li4Ti4.95Ta0.05O12.Ta-doping does not change the phase composition and particle morphology,while improves remarkably its cycling stability at high charge/discharge rate.Li4Ti4.95Ta0.05O12 exhibits an excellent rate capability with a reversible capacity of 116.1 mA·h/g at 10C and even 91.0 mA·h/g at 30C.The substitution of Ta for Ti site can enhance the electronic conductivity of Li4Ti5O12 via the generation of mixing Ti4＋/Ti3＋,which indicates that Li4Ti4.95Ta0.05O12 is a promising candidate material for anodes in lithium-ion battery application.展开更多
Co-P （4.9% P） powders with a chain-like morphology were prepared by a novel chemical reduction method. The Co-P and germanium powders were mixed at various mass ratios to form Co-P composite electrodes. Charge and d...Co-P （4.9% P） powders with a chain-like morphology were prepared by a novel chemical reduction method. The Co-P and germanium powders were mixed at various mass ratios to form Co-P composite electrodes. Charge and discharge test and electrochemical impedance spectroscopy （EIS） were carried out to investigate the electrochemical performance, which can be significantly improved by the addition of germanium. For instance, when the mass ratio of Co-P powders to germanium is 5：1, the sample electrode shows a reversible discharge capacity of 350.3 mA·h/g and a high capacity retention rate of 95.9% after 50 cycles. The results of cyclic voltammmetry （CV） show the reaction mechanism of Co/Co（OH）2 within Co-P composite electrodes and EIS indicates that this electrode shows a low charge-transfer resistance, facilitating the oxidation of Co to Co（OH）2.展开更多
A facile ultrasonic method was used to synthesize CoO/graphene nanohybrids by employing Co4（CO）12 as a cobalt precursor. The nanohybrids were characterized by SEM, TEM and XPS, and the results show that CoO nanopart...A facile ultrasonic method was used to synthesize CoO/graphene nanohybrids by employing Co4（CO）12 as a cobalt precursor. The nanohybrids were characterized by SEM, TEM and XPS, and the results show that CoO nanoparticles （3-5 nm） distribute uniformly on the surface of graphene. The CoO/graphene nanohybrids display high performance as an anode material for lithium-ion battery, such as high reversible lithium storage capacity （650 mA-h/g after 50 cycles, almost twice that of commercial graphite anode）, high coulombic efficiency （over 95%） and excellent cycling stability. The extraordinary performance arises from the structure of the nanohybrids： the nanosized CoO particles with high dispersity on conductive graphene substrates are beneficial for lithium-ion insertion/extraction, shortening diffusion length for lithium ions and improving conductivity, thus the lithium storage performance was improved.展开更多
With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ...With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ion battery is promising to replace the lithium-ion battery in the field of large-scale energy storage by virtue of its low price and environmental friendliness.At present,the research on the anode materials of potassium ion batteries mainly focuses on carbon materials and the design of various nanostructured metal-based materials.Problems such as poor rate performance and inferior cycle life caused by electrode structure comminution during charge and discharge have not been solved.Quantum dots/nanodots materials are a new type of nanomaterials that can effectively improve the utilization of electrode materials and reduce production costs.In addition,quantum dots/nanodots materials can enhance the electrode reaction kinetics,reduce the stress generated in cycling,and effectively alleviate the agglomeration and crushing of electrode materials.In this review,we will systematically introduce the synthesis methods,K+storage properties and K+storage mechanisms of carbon quantum dots and carbon-based transition metal compound quantum dots composites.This review will have significant references for potassium ion battery researchers.展开更多
Since lithium-ion batteries(LIBs) have been substantially researched in recent years, they now possess exceptional energy and power densities, making them the most suited energy storage technology for use in developed...Since lithium-ion batteries(LIBs) have been substantially researched in recent years, they now possess exceptional energy and power densities, making them the most suited energy storage technology for use in developed and developing industries like stationary storage and electric cars, etc. Concerns about the cost and availability of lithium have prompted research into alternatives, such as sodium-ion batteries(SIBs), which use sodium instead of lithium as the charge carrier. This is especially relevant for stationary applications, where the size and weight of battery are less important. The working efficiency and capacity of these batteries are mainly dependent on the anode, cathode, and electrolyte. The anode,which is one of these components, is by far the most important part of the rechargeable battery.Because of its characteristics and its structure, the anode has a tremendous impact on the overall performance of the battery as a whole. Keeping the above in view, in this review we critically reviewed the different types of anodes and their performances studied to date in LIBs and SIBs. The review article is divided into three main sections, namely:(i) intercalation reaction-based anode materials;(ii) alloying reaction-based anode materials;and(iii) conversion reaction-based anode materials, which are further classified into a number of subsections based on the type of material used. In each main section, we have discussed the merits and challenges faced by their particular system. Afterward, a brief summary of the review has been discussed. Finally, the road ahead for better application of Li/Na-ion batteries is discussed, which seems to mainly depend on exploring the innovative materials as anode and on the inoperando characterization of the existing materials for making them more capable in terms of application in rechargeable batteries.展开更多
Aluminum is an innovative anode material for seawater battery. But large polarization and low electrochemical activity restrict its application. In this research, A1-Mg-Sn-Hg-Ce anode materials were prepared and the m...Aluminum is an innovative anode material for seawater battery. But large polarization and low electrochemical activity restrict its application. In this research, A1-Mg-Sn-Hg-Ce anode materials were prepared and the microstructures were investigated by scanning electron microscopy （SEM）. The electrochemical properties of A1-Mg-Sn-Hg-Ce anode materials were measured by potentiodynamic polarization and potential-time discharge in a 4.5 wt.%NaOH solution at 353 K. The results indicated that the increasing content of cerium addition refined the grain structure of A1-Mg-Sn-Hg alloy and promoted the uniform distribution of Sn and Hg elements in A1 matrix. The morphology of second phases changed from disperse granular to intergranulate strip with the increasing content of cerium addition in AI-Mg-Sn-Hg alloy. During the half-cell tests at a 650 mA/cm3 current density, the discharge activity of AI-Mg-Sn-Hg-Ce alloy was improved with the increasing content of cerium addition. The average discharge potential of AI-Mg-Sn-Hg-0.3 wt.%Ce alloy was -1.721 V （vs. SCE）, which was more negative than -1.406 V （vs. SCE） in AZglD. The best corrosion resistance occurred in A1-Mg-Sn-Hg-0.05 wt.%Ce alloy with the corrosion current density, 18.84± 2.21 mA/cm2. The corrosion behaviours of A1-Mg-Sn-Hg-Ce alloys were also analyzed.展开更多
基金National Key Research and Development Program of China (2022YFB2402200)National Natural Science Foundation of China (22225201,22379028)+2 种基金Fundamental Research Funds for the Central Universities (20720220010)Shanghai Pilot Program for Basic Research–Fudan University 21TQ1400100 (21TQ009)Key Basic Research Program of Science and Technology Commission of Shanghai Municipality (23520750400)。
文摘Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials for SIBs are mainly used as cathodes because of their relatively high redox potentials(>1 V).Organic electrodes with low redox potential that can be used as anode are rare.Herein,a novel organic anode material (tetrasodium 1,4,5,8-naphthalenetetracarboxylate,Na_(4)TDC) has been developed with low redox potential (<0.7 V) and excellent cyclic stability.Its three-sodium storage mechanism was demonstrated with various in-situ/ex-situ spectroscopy and theoretical calculations,showing a high capacity of 208 mAh/g and an average decay rate of merely 0.022%per cycle.Moreover,the Na_(4)TDC-hard carbon composite can further acquire improved capacity and cycling stability for 1200 cycles even with a high mass loading of up to 20 mg cm^(-2).By pairing with a thick Na_(3)V_(2)(PO_(4))_(3)cathode (20.6 mg cm^(-2)),the as-fabricated full cell exhibited high operating voltage (2.8 V),excellent rate performance and cycling stability with a high capacity retention of 88.7% after 200 cycles,well highlighting the Na_(4)TDC anode material for SIBs.
基金financially supported by the Research Project Supported by Shanxi Scholarship Council of China(No.2022-049)the Natural Science Foundation of Shanxi Province,China(No.20210302123167)。
文摘Carbon materials are widely recognized as highly promising electrode materials for various energy storage system applications.Coal tar residues(CTR),as a type of carbon-rich solid waste with high value-added utilization,are crucially important for the development of a more sustainable world.In this study,we employed a straightforward direct carbonization method within the temperature range of 700-1000℃to convert the worthless solid waste CTR into economically valuable carbon materials as anodes for potassium-ion batteries(PIBs).The effect of carbonization temperature on the microstructure and the potassium ions storage properties of CTR-derived carbons(CTRCs)were systematically explored by structural and morphological characterization,alongside electrochemical performances assessment.Based on the co-regulation between the turbine layers,crystal structure,pore structure,functional groups,and electrical conductivity of CTR-derived carbon carbonized at 900℃(CTRC-900H),the electrode material with high reversible capacity of 265.6m Ah·g^(-1)at 50 m A·g^(-1),a desirable cycling stability with 93.8%capacity retention even after 100 cycles,and the remarkable rate performance for PIBs were obtained.Furthermore,cyclic voltammetry(CV)at different scan rates and galvanostatic intermittent titration technique(GITT)have been employed to explore the potassium ions storage mechanism and electrochemical kinetics of CTRCs.Results indicate that the electrode behavior is predominantly governed by surface-induced capacitive processes,particularly under high current densities,with the potassium storage mechanism characterized by an“adsorption-weak intercalation”mechanism.This work highlights the potential of CTR-based carbon as a promising electrode material category suitable for high-performance PIBs electrodes,while also provides valuable insights into the new avenues for the high value-added utilization of CTR.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.RS-2024-00453815)Korea Institute of Energy Technology Evaluation and Planning(KETEP)grant funded by the Korea government(MOTIE)(20228510070100)。
文摘Recently,potassium-ion batteries(PIBs)have received significant attention in the energy storage field owing to their high-power output,fast charging capability,natural abundance,and environmental sustainability.Herein,we comprehensively review recent advancements in the design and development of carbon-based anode materials for PIBs anodes,covering graphite,hard carbon,alloy and conversion materials with carbon,and carbon host for K metal deposition.Chemical strategies such as structural engineering,heteroatom-doping,and surface modifications are highlighted to improve electrochemical performances as well as to resolve technical challenges,such as electrode instability,low initial Coulombic efficiency,and electrolyte compatibility.Furthermore,we discuss the fundamental understanding of potassium-ion storage mechanisms of carbon-based materials and their correlation with electrochemical performance.Finally,we present the current challenges and future research directions for the practical implementation of carbon-based anodes to enhance their potential as next-generation energy storage materials for PIBs.This review aims to provide our own insights into innovative design strategies for advanced PIB's anode through the chemical and engineering strategies.
基金the Khalifa University of Science and Technology through the internal grant RIG-2023-01.
文摘The discovery of novel materials with compelling properties is more accessible with the help of advanced computational algorithms.Recent experimental synthesis of the biphenylene network(C_(6))motivated us to discover new BN-doped biphenylene networks(C_(4)BN,C_(2)B_(2)N_(2),and B_(4)N_(4))and their applications in Li(K)-ion batteries using an evolutionary algorithm and the first-principles calculations.The thermodynamic,thermal,and mechanical stability calculations and decomposition energy suggest the experimental synthesis of predicted biphenylene networks.Adding BN in the biphenylene networks shows a transition from metal to semimetal to semiconductor.The BN biphenylene network shows an HSE06 band gap of 3.06 eV,smaller than h-BN.The C_(4)BN and C_(2)B_(2)N_(2)biphenylene networks offer Li(K)adsorption energy of-0.56 eV(-0.81 eV)and-0.14 eV(-0.28 eV),respectively,with a low diffusion barrier of 178 meV(58 meV)and 251 meV(79 meV),and a large diffusion constant of 8.50×10^(-5)cm^(2)=s(8.78×10^(-3)cm^(2)=s)and 5.33×10^(-6)cm^(2)=s(4.12×10^(-3)cm^(2)=s),respectively.The calculated Li(K)theoretical capacity of C_(4)BN and C_(2)B_(2)N_(2)biphenylene networks is 940.21 mA h g^(-1)(899.01 mA h g^(-1))and 768.08 mA h g^(-1)(808.47 mA h g^(-1)),with a low open circuit voltage of 0.34 V(0.23 V),and 0.17 V(0.13 V),resulting in very high energy density of 2576.18 mW h g^(-1)(2445.31 mW h g^(-1))and 2181.35 mW h g^(-1)(2263.72 mW h g^(-1)),respectively.Only a slight volume change of 1.6%confirms the robustness of BN-doped carbon-based biphenylene networks.Our findings present novel 2D BN-doped biphenylene networks and a pathway toward their applications in metal-ion batteries.
基金supported by National Natural Science Foundation,China(Nos.52071132,U21A20284 and 52261135632)Natural Science Foundation of Henan,China(Nos.232300421080,242300421035)+2 种基金Program for Innovative Team(in Science and Technology)in University of Henan Province,China(No.24IRTSTHN006)Key Scientific Research Programs in Universities of Henan Province,China–Special Projects for Basic Research(No.23ZX008)the Natural Science Foundation of Hunan Province,China(No.2023JJ50287)。
文摘Conjugated microporous polymers(CMPs)have attracted considerable attention as potential organic anode materials for sodium-ion batteries(SIBs)due to their flexible chemical structure,high porosity,environmental friendliness,and cost effectiveness.However,the inherent shortcomings of organic electrodes,such as low conductivity,high solubility in electrolyte,narrow material utilization,etc.,limit their further development.In this work,we successfully prepared a novel porous polyimide PPD containing multicarbonyl active centers via the polycondensation of pyromellitic dianhydride(PMDA)and2,6-diaminoanthraquinone(DAAQ).The stable conjugated structure and multiple redox centers give the polymer high reversible specific capacity(244.6 m Ah/g after 100 cycles at 100 m A/g),ultra-long cycle stability(100.7 m Ah/g after 2000 cycles at 1.0 A/g),and predominant rate capability.Meanwhile,the sodium storage mechanism of the electrode materials during the charging and discharging process is investigated by ex-situ XPS/FTIR analysis.Due to the exceptional electrochemical properties and simple synthesis method,this work may shed light on the preparation of polyimide-based anodes for high specific capacity and rate capability secondary batteries.
基金supported by Guangdong Basic and Applied Basic Research Foundation(Nos.2021A1515110164 and 2022A1515010208)the National Natural Science Foundation of China(No.52207248)the Open Testing Foundation of Analytical&Testing Center of Northwestern Polytechnical University(No.2022T024).
文摘Conversion-alloying anode materials are competitive candidates for high-energy-density sodium-ion batteries(SIBs).However,the sluggish dynamics and severe volume expansion during Na insertion/extraction become the key bottlenecks hindering their application in SIBs.Herein,SnTe nanoparticles are anchored on reduced graphene oxide(rGO)and encapsulated by nitrogen-doped carbon(NC)to construct SnTe@rGO@NC composite as anode for SIBs,where hierarchical confinement effect can provide a buffer area to accommodate huge volume expansion as well as enhance electronic conductivity and Na-ion transfer kinetics behavior,confirmed by density functional theory(DFT)calculation and experimental study.Meanwhile,structural stability and interfacial charge transfer of the composite can be further improved by the strong chemical bonds of C-Sn and C-Te.High-angle annular dark field scanning transmission electron microscopy visually at atomic scale declares that SnTe@rGO@NC proceeds conversion-alloying dual-mechanism for Na-ion storage employing Sn as redox center(4SnTe+23Na^(+)+23e^(-)→Na_(15)Sn_(4)+4Na_(2)Te).Thus,SnTe@rGO@NC architecture displays a high reversible specific capacity of 261.5 mAh·g^(-1)at 50 mA·g^(-1),superior rate capability and excellent cycling stability with long-term lifespan over 1000 cycles at 200 mA·g^(-1).The multi-physicochemical encapsulation strategy sheds light on the development of a high-performance conversion-alloying anode for SIBs.
基金supported by the National Natural Science Foundation of China(22209057)the Guangzhou Basic and Applied Basic Research Foundation(2024A04J0839).
文摘Potassium-ion batteries(PIBs)are considered as a promising energy storage system owing to its abundant potassium resources.As an important part of the battery composition,anode materials play a vital role in the future development of PIBs.Bismuth-based anode materials demonstrate great potential for storing potassium ions(K^(+))due to their layered structure,high theoretical capacity based on the alloying reaction mechanism,and safe operating voltage.However,the large radius of K^(+)inevitably induces severe volume expansion in depotassiation/potassiation,and the sluggish kinetics of K^(+)insertion/extraction limits its further development.Herein,we summarize the strategies used to improve the potassium storage properties of various types of materials and introduce recent advances in the design and fabrication of favorable structural features of bismuth-based materials.Firstly,this review analyzes the structure,working mechanism and advantages and disadvantages of various types of materials for potassium storage.Then,based on this,the manuscript focuses on summarizing modification strategies including structural and morphological design,compositing with other materials,and electrolyte optimization,and elucidating the advantages of various modifications in enhancing the potassium storage performance.Finally,we outline the current challenges of bismuth-based materials in PIBs and put forward some prospects to be verified.
文摘The urgent demand for clean energy solutions has intensified the search for advanced storage materials,with rechargeable alkali-ion batteries(AIBs)playing a pivotal role in electrochemical energy storage.Enhancing electrode performance is critical to addressing the increasing need for high-energy and high-power AIBs.Next-generation anode materials face significant challenges,including limited energy storage capacities and complex reaction mechanisms that complicate structural modeling.Sn-based materials have emerged as promising candidates for AIBs due to their inherent advantages.Recent research has increasingly focused on the development of heterojunctions as a strategy to enhance the performance of Sn-based anode materials.Despite significant advances in this field,comprehensive reviews summarizing the latest developments are still sparse.This review provides a detailed overview of recent progress in Sn-based heterojunction-type anode materials.It begins with an explanation of the concept of heterojunctions,including their fabrication,characterization,and classification.Cutting-edge research on Sn-based heterojunction-type anodes for AIBs is highlighted.Finally,the review summarizes the latest advancements in heterojunction technology and discusses future directions for research and development in this area.
基金financial support provided by the NORPART-2021/10355 project,funded by the Norwegian Directorate for Higher Education and Skills(HK-Dir)。
文摘The scarcity and high cost of lithium resources drive the search for sustainable alternatives,positioning potassium-ion batteries(KIBs)as promising energy storage solutions due to the natural abundance and advantageous electrochemical properties of the potassium.This study investigates the enhancement of KIB anodes through phase transformation and electronic structure engineering of monolayer 1T-MoS_(2),achieved via doping with highly electronegative non-metal elements:carbon(C),nitrogen(N),oxygen(O),and fluorine(F).Density functional theory(DFT)simulations reveal that electronegative atom doping enhances phase stability,structural robustness,and thermal resilience,which are key properties for highperformance KIB anodes.Among the doped configurations,F and N-doped 1T-MoS_(2)(MoS_(2-)F and MoS_(2)-N)exhibit superior electrochemical performance,showing optimal adsorption energies and significantly improved electronic conductivity,attributable to favorable charge redistribution and increased active potassium adsorption sites.Specifically,MoS_(2)-F and MoS_(2)-N achieve the highest specific capacities of339.65 and 339.17 mAh/g,respectively,while maintaining stability within an ideal open circuit voltage range,outperforming undoped MoS_(2).This work undersco res the potential of electronegative atom doping in 1T-MoS_(2)to enable sustainable,high-capacity energy storage solutions,offering key advancements in the electrochemical and structural properties of KIB anodes.
基金supported by the Henan Province Science and Technology Research Project(No.232102241006)the National Key Research and Development Program of China(No.2020YFB1713500)+2 种基金Opening Project of National Joint Engineering Research Center for Abrasion Control and Molding of Metal Materials&Henan Key Laboratory of High-temperature Structural and Functional Materials,Henan University of Science and Technology(No.HKDNM2019013)the Open Fund of State Key Laboratory of Advanced Refractories(No.SKLAR202210)the Major Science and Technology Projects of Henan Province(No.221100230200)。
文摘Lithium metal is one of the most promising anodes for lithium batteries because of their high theoretical specific capacity and the low electrochemical potential.However,the commercialization of lithium metal anodes(LMAs)is facing significant obstacles,such as uncontrolled lithium dendrite growth and unstable solid electrolyte interface,leading to inferior Coulombic efficiency,unsatisfactory cycling stability and even serious safety issues.Introducing low-cost natural clay-based materials(NCBMs)in LMAs is deemed as one of the most effective methods to solve aforementioned issues.These NCBMs have received considerable attention for stabilizing LMAs due to their unique structure,large specific surface areas,abundant surface groups,high mechanical strength,excellent thermal stability,and environmental friendliness.Considering the rapidly growing research enthusiasm for this topic in the last several years,here,we review the recent progress on the application of NCBMs in stable and dendrite-free LMAs.The different structures and modification methods of natural clays are first summarized.In addition,the relationship between their modification methods and nano/microstructures,as well as their impact on the electrochemical properties of LMAs are systematically discussed.Finally,the current challenges and opportunities for application of NCBMs in stable LMAs are also proposed to facilitate their further development.
基金financially supported by the National Natural Science Foundation of China(No.22209057)the Guangzhou Basic and Applied Basic Research Foundation(No.2024A04J0839)。
文摘Thanks to its abundant reserves,relatively high energy density,and low reduction potential,potassium ion batteries(PIBs)have a high potential for large-scale energy storage applications.Due to the large radius of potassium ions,most conventional anode materials undergo severe volume expansion,making it difficult to achieve stable and reversible energy storage.Therefore,developing high-performance anode materials is one of the critical factors in developing PIBs.In this sense,antimony(Sb)-based anode materials with high theoretical capacity and safe reaction potentials have a broad potential for application in PIBs.However,overcoming the rapid capacity decay induced by the large radius of potassium ions is still an issue that needs to be focused on.This paper reviews the latest research on different types of Sb-based anode materials and provides an in-depth analysis of their optimization strategies.We focus on material selection,structural design,and storage mechanisms to develop a detailed description of the material.In addition,the current challenges still faced by Sb-based anode materials are summarized,and some further optimization strategies have been added.We hope to provide some insights for researchers developing Sb-based anode materials for next-generation advanced PIBs.
基金supported by“regional innovation mega project”program through the Korea Innovation Foundation funded by Ministry of Science and ICT(Project Number:2023-DD-UP-0026)the Energy Technology Evaluation and Planning(KETEP)and the Ministry of Trade,Industry&Energy(MOTIE)(No.RS-2024-00509401,RS-2023-00217581)“Regional Innovation Strategy(RIS)”through the National Research Foundation of Korea(NRF)funded by the Ministry of Education(MOE)(2021RIS-001).
文摘High-performance lithium-ion batteries and sodium-ion batteries have been developed utilizing a hybrid anode material composed of zinc sulfide/sulfurized polyacrylonitrile.The in situ-generated zinc sulfide nanoparticles serve as catalytic agents,significantly enhancing conductivity,shortening diffusion paths,and accelerating reaction kinetics.Simultaneously,the sulfurized polyacrylonitrile fibers form a three-dimensional matrix that not only provides a continuous network for rapid electron transfer but also prevents zinc sulfide nanoparticle aggregation and mitigates volume changes during charge-discharge cycles.Moreover,the heterointerface structure at the junction of zinc sulfide nanoparticles and the sulfurized polyacrylonitrile matrix increases the availability of active sites and facilitates both ion adsorption and electron transfer.As an anode material for lithium-ion batteries,the zinc sulfide/sulfurized polyacrylonitrile hybrid demonstrates a high reversible capacity of 1178 mAh g^(-1)after 100 cycles at a current density of 0.2 A g^(-1),maintaining a capacity of 788 mAh g^(-1)after 200 cycles at 1 A g^(-1).It also exhibits excellent sodium storage capabilities,retaining a capacity of 625 mAh g^(-1)after 150 cycles at 0.2 A g^(-1).Furthermore,ex-situ X-ray photoelectron spectroscopy,X-ray diffraction,7Li solid-state magic angle spinning nuclear magnetic resonance,and in situ Raman are employed to investigate the reaction mechanisms of the zinc sulfide/sulfurized polyacrylonitrile hybrid anode,providing valuable insights that pave the way for the advancement of hybrid anode materials in lithium-ion batteries and sodium-ion batteries.
基金financially supported by the National Natural Science Foundation of China(Nos.22302133 and 22405161)Central Guidance on Local Science and Technology Development Fund of Hebei Province,China(No.236Z4406G)+5 种基金the Natural Science Foundation of Hebei Education Department,China(No.BJ2025100)the Natural Science Foundation of Hebei Province,China(No.B2021210001)the Natural Science Foundation of Xinjiang Uygur Autonomous Region(No.2024D01A157)the Key R&D Plan of Karamay(No.2024zdyf0009)Karamay Innovation Environment Construction Plan(Innovative Talents)Project(No.2024hjcxrc0029)the Research Foundation of China University of Petroleum-Beijing at Karamay(No.XQZX20240023)
文摘Tin dioxide(SnO_(2))with a high theoretical specific capacity of 1494 mAh g^(-1)is a promising candidate anode material for lithium storage.However,the shortcomings of serious volume expansion and low conductivity limit its wide application.Herein,coaxial nano-multilayered C/SnO_(2)/TiO_(2)composites were fabricated via layerby-layer self-assembly of TiO_(2)and SnO_(2)-gel layers on the natural cellulose filter paper,followed by thermal treatment under a nitrogen atmosphere.Through engineering design of the assembly process,the optimal C/SinO_(2)/TiO_(2)composite features five alternating SnO_(2)and TiO_(2)nanolayers,with TiO_(2)as the outside shell(denoted as C/TSTST).This unique structure endows the C/TSTST with excellent structural stability and electrochemical kinetics,making it a high-performance anode for lithium-ion batteries(LIBs).The C/TSTST composite delivers a high reversible capacity of 676 mAh g^(-1)at 0.1 A g^(-1)after 200 cycles and retains a capacity of 504 mAh g^(-1)at 1.0 A g^(-1),which can be recovered to 781 mAh g^(-1)at 0.1 A g^(-1)The significantly enhanced electrochemical performance is attributed to the hierarchical hybrid structure,where the carbon core combined with coaxial TiO_(2)nanolayers serves as a structural scaffold,ameliorating volume change of SnO_(2)while creating abundant interfacial defects for enhanced lithium storage and rapid charge transport.These findings are further demonstrated by the density functional theory(DFT)calculations.This work provides an efficient strategy for designing coaxial nano-multilayered transition metal oxide-related electrode materials,offering new insights into high-performance LIBs anodes.
基金Project (2014CB643406) supported by the National Basic Research Program of ChinaProject (2011FJ1005) supported by Major Special Project of Science and Technology of Hunan Province,China
文摘A facile way was used to synthesize Cu2O/reduced graphene oxide （rGO） composites with octahedron-like morphology in aqueous solution without any surfactant. TEM images of the obtained Cu2O/rGOs reveal that the Cu2O particles and rGO distribute hierarchically and the primary Cu2O particles are encapsulated well in the graphene nanosheets. The electrochemical performance of Cu2O/rGOs is enhanced compared with bare Cu2O when they are employed as anode materials for lithium ion batteries. The Cu2O/rGO composites maintain a reversible capacity of 348.4 mA？h/g after 50 cycles at a current density of 100 mA/g. In addition, the composites retain 305.8 mA？h/g after 60 cycles at various current densities of 50, 100, 200, 400 and 800 mA/g.
文摘The electrochemical performance of Ta-doped Li4Ti5O12 in the form of Li4Ti4.95Ta0.05O12 was characterized.X-ray diffraction（XRD） and scanning electron microscopy（SEM） were employed to characterize the structure and morphology of Li4Ti4.95Ta0.05O12.Ta-doping does not change the phase composition and particle morphology,while improves remarkably its cycling stability at high charge/discharge rate.Li4Ti4.95Ta0.05O12 exhibits an excellent rate capability with a reversible capacity of 116.1 mA·h/g at 10C and even 91.0 mA·h/g at 30C.The substitution of Ta for Ti site can enhance the electronic conductivity of Li4Ti5O12 via the generation of mixing Ti4＋/Ti3＋,which indicates that Li4Ti4.95Ta0.05O12 is a promising candidate material for anodes in lithium-ion battery application.
基金Project supported by the Priority Academic Program Development of Jiangsu Higher Education Institutions of ChinaProject(CXLX11_0359)supported by Research Innovative Projects for Average College Graduate Students of 2011 in Jiangsu Province,China+2 种基金Project(RERU2011010)supported by Open Subject of State Key Laboratory of Rare Earth Resource Utilization,ChinaProject(51201089)supported by the National Natural Science Foundation of ChinaProject(CPSF2012M521064)supported by China Postdoctoral Science Foundation
文摘Co-P （4.9% P） powders with a chain-like morphology were prepared by a novel chemical reduction method. The Co-P and germanium powders were mixed at various mass ratios to form Co-P composite electrodes. Charge and discharge test and electrochemical impedance spectroscopy （EIS） were carried out to investigate the electrochemical performance, which can be significantly improved by the addition of germanium. For instance, when the mass ratio of Co-P powders to germanium is 5：1, the sample electrode shows a reversible discharge capacity of 350.3 mA·h/g and a high capacity retention rate of 95.9% after 50 cycles. The results of cyclic voltammmetry （CV） show the reaction mechanism of Co/Co（OH）2 within Co-P composite electrodes and EIS indicates that this electrode shows a low charge-transfer resistance, facilitating the oxidation of Co to Co（OH）2.
基金Project (4340142501) supported by Start-up Funds of Chair Professor, Tongji University, ChinaProject (51173135) supported by the National Natural Science Foundation of China
文摘A facile ultrasonic method was used to synthesize CoO/graphene nanohybrids by employing Co4（CO）12 as a cobalt precursor. The nanohybrids were characterized by SEM, TEM and XPS, and the results show that CoO nanoparticles （3-5 nm） distribute uniformly on the surface of graphene. The CoO/graphene nanohybrids display high performance as an anode material for lithium-ion battery, such as high reversible lithium storage capacity （650 mA-h/g after 50 cycles, almost twice that of commercial graphite anode）, high coulombic efficiency （over 95%） and excellent cycling stability. The extraordinary performance arises from the structure of the nanohybrids： the nanosized CoO particles with high dispersity on conductive graphene substrates are beneficial for lithium-ion insertion/extraction, shortening diffusion length for lithium ions and improving conductivity, thus the lithium storage performance was improved.
基金financial support from the Doctoral Foundation of Henan University of Engineering(No.D2022025)National Natural Science Foundation of China(No.U2004162)+1 种基金National Natural Science Foundation of China(No.52302138)Key Project for Science and Technology Development of Henan Province(No.232102320221)。
文摘With the rapid development of electric vehicles,hybrid electric vehicles and smart grids,people's demand for large-scale energy storage devices is increasingly intense.As a new type of secondary battery,potassium ion battery is promising to replace the lithium-ion battery in the field of large-scale energy storage by virtue of its low price and environmental friendliness.At present,the research on the anode materials of potassium ion batteries mainly focuses on carbon materials and the design of various nanostructured metal-based materials.Problems such as poor rate performance and inferior cycle life caused by electrode structure comminution during charge and discharge have not been solved.Quantum dots/nanodots materials are a new type of nanomaterials that can effectively improve the utilization of electrode materials and reduce production costs.In addition,quantum dots/nanodots materials can enhance the electrode reaction kinetics,reduce the stress generated in cycling,and effectively alleviate the agglomeration and crushing of electrode materials.In this review,we will systematically introduce the synthesis methods,K+storage properties and K+storage mechanisms of carbon quantum dots and carbon-based transition metal compound quantum dots composites.This review will have significant references for potassium ion battery researchers.
文摘Since lithium-ion batteries(LIBs) have been substantially researched in recent years, they now possess exceptional energy and power densities, making them the most suited energy storage technology for use in developed and developing industries like stationary storage and electric cars, etc. Concerns about the cost and availability of lithium have prompted research into alternatives, such as sodium-ion batteries(SIBs), which use sodium instead of lithium as the charge carrier. This is especially relevant for stationary applications, where the size and weight of battery are less important. The working efficiency and capacity of these batteries are mainly dependent on the anode, cathode, and electrolyte. The anode,which is one of these components, is by far the most important part of the rechargeable battery.Because of its characteristics and its structure, the anode has a tremendous impact on the overall performance of the battery as a whole. Keeping the above in view, in this review we critically reviewed the different types of anodes and their performances studied to date in LIBs and SIBs. The review article is divided into three main sections, namely:(i) intercalation reaction-based anode materials;(ii) alloying reaction-based anode materials;and(iii) conversion reaction-based anode materials, which are further classified into a number of subsections based on the type of material used. In each main section, we have discussed the merits and challenges faced by their particular system. Afterward, a brief summary of the review has been discussed. Finally, the road ahead for better application of Li/Na-ion batteries is discussed, which seems to mainly depend on exploring the innovative materials as anode and on the inoperando characterization of the existing materials for making them more capable in terms of application in rechargeable batteries.
基金supported by National Natural Science Foundation of China(51101171)the Specialized Research Fund for the Doctor Program of Higher Education(20110162120051)
文摘Aluminum is an innovative anode material for seawater battery. But large polarization and low electrochemical activity restrict its application. In this research, A1-Mg-Sn-Hg-Ce anode materials were prepared and the microstructures were investigated by scanning electron microscopy （SEM）. The electrochemical properties of A1-Mg-Sn-Hg-Ce anode materials were measured by potentiodynamic polarization and potential-time discharge in a 4.5 wt.%NaOH solution at 353 K. The results indicated that the increasing content of cerium addition refined the grain structure of A1-Mg-Sn-Hg alloy and promoted the uniform distribution of Sn and Hg elements in A1 matrix. The morphology of second phases changed from disperse granular to intergranulate strip with the increasing content of cerium addition in AI-Mg-Sn-Hg alloy. During the half-cell tests at a 650 mA/cm3 current density, the discharge activity of AI-Mg-Sn-Hg-Ce alloy was improved with the increasing content of cerium addition. The average discharge potential of AI-Mg-Sn-Hg-0.3 wt.%Ce alloy was -1.721 V （vs. SCE）, which was more negative than -1.406 V （vs. SCE） in AZglD. The best corrosion resistance occurred in A1-Mg-Sn-Hg-0.05 wt.%Ce alloy with the corrosion current density, 18.84± 2.21 mA/cm2. The corrosion behaviours of A1-Mg-Sn-Hg-Ce alloys were also analyzed.
