The growing concern for energy efficiency and the increasing deployment of intermittent renewable energies has led to the development of technologies for capturing,storing,and discharging energy.Supercapacitors can be...The growing concern for energy efficiency and the increasing deployment of intermittent renewable energies has led to the development of technologies for capturing,storing,and discharging energy.Supercapacitors can be considered where batteries do not meet the requirements.However,supercapacitors in systems with a slower charge/discharge cycle,such as photovoltaic systems(PVS),present other obstacles that make replacing batteries more challenging.An extensive literature review unveils a knowledge gap regarding a methodological comparison of batteries and supercapacitors.In this study,we address the technological feasibility of intermittent renewable energy generation systems,focusing on storage solutions for PVS energy.We propose a framework according to one of the essential parameters for their application in PVS:Energy Density or Specific Energy(Wh/kg).Through computational modelling,issues related to the intermittency and seasonality of the solar energy source are addressed,evaluating the possible benefits of implementing batteries,supercapacitors,and hybrid solutions in renewable energy generation systems.Also,the characteristics of two hypothetical configurations of photovoltaic systems,off-grid and on-grid,were analysed.This analysis highlights the characteristics of totally isolated systems(e.g.,on an island or remote village)and systems connected to the grid(e.g.,solar farms),where eliminating the use of batteries can bring significant benefits,in addition to tax incentives,which are decisive in the investment decision-making process.The results clarify the viability of PVS and allow an understanding of parameters that can support the technical decision process between isolated or non-isolated systems,reflecting economic and financial issues.展开更多
In order to meet the demands of new-generation electric vehicles that require high power output(over 15 kW/kg),it is crucial to increase the energy density of car-bon-based supercapacitors to a level comparable to tha...In order to meet the demands of new-generation electric vehicles that require high power output(over 15 kW/kg),it is crucial to increase the energy density of car-bon-based supercapacitors to a level comparable to that of batteries,while maintaining a high power density.We re-port a porous carbon material produced by immersing pop-lar wood(PW)sawdust in a solution of KOH and graphene oxide(GO),followed by carbonization.The resulting mater-ial has exceptional properties as an electrode for high-en-ergy supercapacitors.Compared to the material prepared by the direct carbonization of PW,its electrical conductivity was in-creased from 0.36 to 26.3 S/cm.Because of this and a high microporosity of over 80%,which provides fast electron channels and a large ion storage surface,when used as the electrodes for a symmetric supercapacitor,it gave a high energy density of 27.9 Wh/kg@0.95 kW/kg in an aqueous electrolyte of 1.0 mol/L Na_(2)SO_(4).The device also had battery-level energy storage with maximum energy densities of 73.9 Wh/kg@2.0 kW/kg and 67.6 Wh/kg@40 kW/kg,an ultrahigh power density,in an organic electrolyte of 1.0 mol/L TEABF4/AN.These values are comparable to those of 30−45 Wh/kg for Pb-acid batteries and 30−55 Wh/kg for aqueous lithium batteries.This work indicates a way to prepare carbon materials that can be used in supercapacit-ors with ultrahigh energy and power densities.展开更多
Herein,we developed three-dimensional pristine titanium dioxide(TiO_(2))photo-electrocatalyst material(PEM)with homogeneous distribution of oxygen vacancies(OV)for lithium-oxygen(Li-O_(2))battery system(denoted as LOB...Herein,we developed three-dimensional pristine titanium dioxide(TiO_(2))photo-electrocatalyst material(PEM)with homogeneous distribution of oxygen vacancies(OV)for lithium-oxygen(Li-O_(2))battery system(denoted as LOBs)under illumination.This rationally designed OV-TiO_(2)photoelectrode-catalyst has exhibited excellent capacity,small overpotential,long-term cycle stability,and higher rate capability performance according to our electrochemical experiment study.In short,OV as photoinduced charge separation centers(inert surface atomic modification method)fascinate the effective separation of electrons(e^(−))and holes(h^(+)).In turn,induced e−and h+are beneficial to the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)process.More importantly,machine learning(ML)algorithms to analyze and optimize battery performance are innovative in the photoelectrical field.The utility of ML analysis is extensively shown to be effective in learning the in/output connection of interest.Based on ML analysis results,the OV-TiO_(2)cathode is indeed the key point to extend the LOB life span.More importantly,our brilliant anatase OV-TiO_(2)revealed the optimization of electrode material for high performance and reversibility in LOBs.We expect that it will bring special OV-TiO_(2)and some other hierarchical hollow nanomaterials,a big step toward battery technology no matter in cost-effectiveness and environmentally friendly aspects.展开更多
In order to address the widespread data shortage problem in battery research,this paper proposes a generative adversarial network model that combines it with deep convolutional networks,the Wasserstein distance,and th...In order to address the widespread data shortage problem in battery research,this paper proposes a generative adversarial network model that combines it with deep convolutional networks,the Wasserstein distance,and the gradient penalty to achieve data augmentation.To lower the threshold for implementing the proposed method,transfer learning is further introduced.The W-DC-GAN-GP-TL framework is thereby formed.This framework is evaluated on 3 different publicly available datasets to judge the quality of generated data.Through visual comparisons and the examination of two visualization methods(probability density function(PDF)and principal component analysis(PCA)),it is demonstrated that the generated data is hard to distinguish from the real data.The application of generated data for training a battery state model using transfer learning is further evaluated.Specifically,Bi-GRU-based and Transformer-based methods are implemented on 2 separate datasets for estimating state of health(SOH)and state of charge(SOC),respectively.The results indicate that the proposed framework demonstrates satisfactory performance in different scenarios:for the data replacement scenario,where real data are removed and replaced with generated data,the state estimator accuracy decreases only slightly;for the data enhancement scenario,the estimator accuracy is further improved.The estimation accuracy of SOH and SOC is as low as 0.69%and 0.58%root mean square error(RMSE)after applying the proposed framework.This framework provides a reliable method for enriching battery measurement data.It is a generalized framework capable of generating a variety of time series data.展开更多
Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systemat...Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systematic strategy that rationally optimizes electronic structures and mesoscale transport properties.In this work,we propose an autogenously transformed CoWO_(4)/WO_(2) heterojunction catalyst,integrating a strong polysulfide-adsorbing intercalation catalyst with a metallic-phase promoter for enhanced activity.CoWO_(4) effectively captures polysulfides,while the CoWO_(4)/WO_(2) interface facilitates their S-S bond activation on heterogenous catalytic sites.Benefiting from its directional intercalation channels,CoWO_(4) not only serves as a dynamic Li-ion reservoir but also provides continuous and direct pathways for rapid Li-ion transport.Such synergistic interactions across the heterojunction interfaces enhance the catalytic activity of the composite.As a result,the CoWO_(4)/WO_(2) heterostructure demonstrates significantly enhanced catalytic performance,delivering a high capacity of 1262 mAh g^(−1) at 0.1 C.Furthermore,its rate capability and high sulfur loading performance are markedly improved,surpassing the limitations of its single-component counterparts.This study provides new insights into the catalytic mechanisms governing Li-S chemistry and offers a promising strategy for the rational design of high-performance Li-S battery catalysts.展开更多
Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from...Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from the cathode side.These challenges lead to poor cycle stability and severe self-discharge.From the fabrication and cost point of view,it is technologically more viable to deploy electrolyte engineering than electrode protection strategies.More importantly,a synchronous method for modulation of both cathode and anode is pivotal,which has been often neglected in prior studies.In this work,cationic poly(allylamine hydrochloride)(Pah^(+))is adopted as a low-cost dual-function electrolyte additive for ZIBs.We elaborate the synchronous effect by Pah^(+)in stabilizing Zn anode and immobilizing polyiodide anions.The fabricated Zn-iodine coin cell with Pah^(+)(ZnI_(2) loading:25 mg cm^(−2))stably cycles 1000 times at 1 C,and a single-layered 3.4 cm^(2) pouch cell(N/P ratio~1.5)with the same mass loading cycles over 300 times with insignificant capacity decay.展开更多
Single-atom catalysts(SACs)have garnered significant attention in lithium-sulfur(Li-S)batteries for their potential to mitigate the severe polysulfide shuttle effect and sluggish redox kinetics.However,the development...Single-atom catalysts(SACs)have garnered significant attention in lithium-sulfur(Li-S)batteries for their potential to mitigate the severe polysulfide shuttle effect and sluggish redox kinetics.However,the development of highly efficient SACs and a comprehensive understanding of their structure-activity relationships remain enormously challenging.Herein,a novel kind of Fe-based SAC featuring an asymmetric FeN_(5)-TeN_(4) coordination structure was precisely designed by introducing Te atom adjacent to the Fe active center to enhance the catalytic activity.Theoretical calculations reveal that the neighboring Te atom modulates the local coordination environment of the central Fe site,elevating the d-band center closer to the Fermi level and strengthening the d-p orbital hybridization between the catalyst and sulfur species,thereby immobilizing polysulfides and improving the bidirectional catalysis of Li-S redox.Consequently,the Fe-Te atom pair catalyst endows Li-S batteries with exceptional rate performance,achieving a high specific capacity of 735 mAh g^(−1) at 5 C,and remarkable cycling stability with a low decay rate of 0.038%per cycle over 1000 cycles at 1 C.This work provides fundamental insights into the electronic structure modulation of SACs and establishes a clear correlation between precisely engineered atomic configurations and their enhanced catalytic performance in Li-S electrochemistry.展开更多
Wide-temperature applications of sodium-ion batteries(SIBs)are severely limited by the sluggish ion insertion/diffusion kinetics of conversion-type anodes.Quantum-sized transition metal dichalcogenides possess unique ...Wide-temperature applications of sodium-ion batteries(SIBs)are severely limited by the sluggish ion insertion/diffusion kinetics of conversion-type anodes.Quantum-sized transition metal dichalcogenides possess unique advantages of charge delocalization and enrich uncoordinated electrons and short-range transfer kinetics,which are crucial to achieve rapid low-temperature charge transfer and high-temperature interface stability.Herein,a quantum-scale FeS_(2) loaded on three-dimensional Ti_(3)C_(2) MXene skeletons(FeS_(2) QD/MXene)fabricated as SIBs anode,demonstrating impressive performance under wide-temperature conditions(−35 to 65).The theoretical calculations combined with experimental characterization interprets that the unsaturated coordination edges of FeS_(2) QD can induce delocalized electronic regions,which reduces electrostatic potential and significantly facilitates efficient Na+diffusion across a broad temperature range.Moreover,the Ti_(3)C_(2) skeleton reinforces structural integrity via Fe-O-Ti bonding,while enabling excellent dispersion of FeS_(2) QD.As expected,FeS_(2) QD/MXene anode harvests capacities of 255.2 and 424.9 mAh g^(−1) at 0.1 A g^(−1) under−35 and 65,and the energy density of FeS_(2) QD/MXene//NVP full cell can reach to 162.4 Wh kg^(−1) at−35,highlighting its practical potential for wide-temperatures conditions.This work extends the uncoordinated regions induced by quantum-size effects for exceptional Na^(+)ion storage and diffusion performance at wide-temperatures environment.展开更多
Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental ...Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.展开更多
High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical ...High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical strength,and outstanding catalytic activity.These distinctive characteristics render HEMs highly suitable for various battery components,such as electrodes,electrolytes,and catalysts.This review systematically examines recent advances in the application of HEMs for energy storage,beginning with fundamental concepts,historical development,and key definitions.Three principal categories of HEMs,namely high-entropy alloys,high-entropy oxides,and highentropy MXenes,are analyzed with a focus on electrochemical performance metrics such as specific capacity,energy density,cycling stability,and rate capability.The underlying mechanisms by which these materials enhance battery performance are elucidated in the discussion.Furthermore,the pivotal role of machine learning in accelerating the discovery and optimization of novel high-entropy battery materials is highlighted.The review concludes by outlining future research directions and potential breakthroughs in HEM-based battery technologies.展开更多
Micro-sized anatase TiO_(2) displays inferior capacity as cathode material for magnesium ion batteries because of the higher diffusion energy barrier of Mg^(2+)in anatase TiO_(2) lattice.Herein,we report that nanosize...Micro-sized anatase TiO_(2) displays inferior capacity as cathode material for magnesium ion batteries because of the higher diffusion energy barrier of Mg^(2+)in anatase TiO_(2) lattice.Herein,we report that nanosized anatase TiO_(2) exposed(001)facet doubles the capacity compared to the micro-sized sample ascribed to the interfacial Mg^(2+)ion storage.First-principles calculations reveal that the diffusion energy barrier of Mg^(2+)on the(001)facet is significantly lower than those in the bulk phase and on(100)facet,and the adsorption energy of Mg^(2+)on the(001)facet is also considerably lower than that on(100)facet,which guarantees superior interfacial Mg^(2+)storage of(001)facet.Moreover,anatase TiO_(2) exposed(001)facet displays a significantly higher capacity of 312.9 mAh g^(−1) in Mg-Li dual-salt electrolyte compared to 234.3 mAh g^(−1) in Li salt electrolyte.The adsorption energies of Mg^(2+)on(001)facet are much lower than the adsorption energies of Li+on(001)facet,implying that the Mg^(2+)ion interfacial storage is more favorable.These results highlight that controlling the crystal facet of the nanocrystals effectively enhances the interfacial storage of multivalent ions.This work offers valuable guidance for the rational design of high-capacity storage systems.展开更多
Nitrogen-doped carbon materials with a large specific surface area,high conductivity,and adjustable microstructures have many prospects for energy-related applications.This is especially true for N-doped nanocarbons u...Nitrogen-doped carbon materials with a large specific surface area,high conductivity,and adjustable microstructures have many prospects for energy-related applications.This is especially true for N-doped nanocarbons used in the electrocatalytic oxygen reduction reaction(ORR)and supercapacitors.Here,we report a low-cost,environmentally friendly,large-scale mechanochemical method of preparing N-doped porous carbons(NPCs)with hierarchical micro-mesopores and a large surface area via ball-milling polymerization followed by pyrolysis.The optimized NPC prepared at 1000°C(NPC-1000)offers excellent ORR activity with an onset potential(Eonset)and half-wave potential(E1/2)of 0.9 and 0.82 V,respectively(vs.a reversible hydrogen electrode),which are only approximately 30 mV lower than that of Pt/C.The rechargeable Zn–air battery assembled using NPC-1000 and the NiFe-layered double hydroxide as bifunctional ORR and oxygen evolution reaction electrodes offered superior cycling stability and comparable discharge performance to RuO2 and Pt/C.Moreover,the supercapacitor electrode equipped with NPC prepared at 800℃ exhibited a high specific capacity(431 F g^−1 at 10 mV s^−1),outstanding rate,performance,and excellent cycling stability in an aqueous 6-M KOH solution.This work demonstrates the potential of the mechanochemical preparation method of porous carbons,which are important for energy conversion and storage.展开更多
Lightweight and flexible self-charging power systems with synchronous energy harvesting and energy storage abilities are highly desired in the era of the internet of things and artificial intelligences,which can provi...Lightweight and flexible self-charging power systems with synchronous energy harvesting and energy storage abilities are highly desired in the era of the internet of things and artificial intelligences,which can provide stable,sustainable,and autonomous power sources for ubiquitous,distributed,and low-power wearable electronics.However,there is a lack of comprehensive review and challenging discussion on the state-of-the-art of the triboelectric nanogenetor(TENG)-based self-charging power textiles,which have a great possibility to become the future energy autonomy power sources.Herein,the recent progress of the self-charging power textiles hybridizing fiber/fabric based TENGs and fiber/fabric shaped batteries/supercapacitors is comprehensively summarized from the aspect of textile structural designs.Based on the current research status,the key bottlenecks and brighter prospects of self-charging power textiles are also discussed in the end.It is hoped that the summary and prospect of the latest research of self-charging power textiles can help relevant researchers accurately grasp the research progress,focus on the key scientific and technological issues,and promote further research and practical application process.展开更多
Lithium-ion hybrid supercapacitors(Li-HSCs) and dual-ion batteries(DIBs) are two types of energy storage devices that have attracted extensive research interest in recent years. Li-HSCs and DIBs have similarities in d...Lithium-ion hybrid supercapacitors(Li-HSCs) and dual-ion batteries(DIBs) are two types of energy storage devices that have attracted extensive research interest in recent years. Li-HSCs and DIBs have similarities in device structure, tendency for ion migration, and energy storage mechanisms at the negative electrode. However, these devices have differences in energy storage mechanisms and working potentials at the positive electrode. Here, we first realize the integration of a Li-HSC and a DIB to form a dual-ion hybrid supercapacitor(DIHSC), by employing mesocarbon microbead(MCMB)-based porous graphitic carbon(PGC) with a partially graphitized structure and porous structure as a positive electrode material. The MCMB-PGC-based DIHSC exhibits a novel dual-ion battery-capacitor hybrid mechanism: it exhibits excellent electronic double-layer capacitor(EDLC) behavior like a Li-HSC in the low-middle wide potential range and anion intercalation/de-intercalation behavior like a DIB in the high-potential range. Two types of mechanisms are observed in the electrochemical characterization process, and the energy density of the new DIHSC is significantly increased.展开更多
A novel process is reported which produces an asymmetric supercapacitor through the complete recycling of end-of-life lithium ion batteries.The electrodic powder recovered by industrial scale mechanical treatment of s...A novel process is reported which produces an asymmetric supercapacitor through the complete recycling of end-of-life lithium ion batteries.The electrodic powder recovered by industrial scale mechanical treatment of spent batteries was leached and the dissolved metals were precipitated as mixed metals carbonates.Nanowires battery-type positive electrodes were produced by electrodeposition into nanoporous alumina templates from the electrolytic baths prepared by dissolution of the precipitated carbonates.The impact of the different metals contained in the electrodic powder was evaluated by benchmarking the electrochemical performances of the recovered nanowires-based electrodes against electrodes produced by using high-purity salts.Presence of inactive Cu in the nanowires lowered the final capacitance of the electrodes while Ni showed a synergistic effect with cobalt providing a higher capacitance with respect to synthetic Co electrodes.The carbonaceous solid recovered after leaching was indepth characterized and tested as negative electrode.Both the chemical and electrochemical characterization indicate that the recovered graphite is characterized by the presence of oxygen functionalities introduced by the leaching treatment.This has led to the obtainment of a recovered graphite characterized by an XPS C/O ratio,Raman spectrum and morphology close to literature reports for reduced graphene oxide.The asymmetric supercapacitor assembled using the recovered nanowires-based positive electrodes and graphite as negative electrodes has shown a specific capacitance of 42 F g^(-1), computed including the whole weight of the positive electrode and recovered graphite,providing a maximum energy density of ~9 Wh kg^(-1) and a power density of 416 W kg^(-1) at 2.5 mA cm^(-2).展开更多
As promising energy storage systems,lithium-sulfur(Li-S)batteries have attracted significant attention because of their ultra-high energy densities.However,Li-S battery suffers problems related to the complex phase co...As promising energy storage systems,lithium-sulfur(Li-S)batteries have attracted significant attention because of their ultra-high energy densities.However,Li-S battery suffers problems related to the complex phase conversion that occurs during the charge-discharge process,particularly the deposition of solid Li2S from the liquid-phase polysulfides,which greatly limits its practical application.In this paper,edge-rich MoS2/C hollow microspheres(Edg-MoS2/C HMs)were designed and used to functionalize separator for Li-S battery,resulting in the uniform deposition of Li2S.The microspheres were fabricated through the facile hydrothermal treatment of MoO3-aniline nanowires and a subsequent carbonization process.The obtained Edg-MoS2/C HMs have a strong chemical absorption capability and high density of Li2S binding sites,and exhibit excellent electrocatalytic performance and can effectively hinder the polysulfide shuttle effect and guide the uniform nucleation and growth of Li2S.Furthermore,we demonstrate that the Edg-MoS2/C HMs can effectively regulate the deposition of Li2S and significantly improve the reversibility of the phase conversion of the active sulfur species,especially at high sulfur loadings and high C-rates.As a result,a cell containing a separator functionalized with Edg-MoS2/C HMs exhibited an initial discharge capacity of 935 mAh g-1 at 1.0 C and maintained a capacity of 494 mAh g-1 after 1000 cycles with a sulfur loading of 1.7 mg cm-2.Impressively,at a high sulfur loading of 6.1 mg cm-2 and high rate of 0.5 C,the cell still delivered a high reversible discharge capacity of 478 mAh g-1 after 300 cycles.This work provides fresh insights into energy storage systems related to complex phase conversions.展开更多
Metal–organic frameworks(MOFs),which are generally considered to be crystalline materials comprising metal centers and organic ligands,have attracted growing attention because of their controllable structures and hig...Metal–organic frameworks(MOFs),which are generally considered to be crystalline materials comprising metal centers and organic ligands,have attracted growing attention because of their controllable structures and high porosity.MOFs based on transition metals(Fe,Co,Ni)are highly effi cient electrode materials for electrochemical energy storage.In this review,the characteristics of Fe-MOFs,Co-MOFs,Ni-MOFs,and their derivatives are summarized,and the relationships between the structures and performance are unveiled in depth.Additionally,their applications in lithium–ion batteries,lithium–sulfur batteries,and supercapacitors are discussed.This review sheds light on the development of MOFs and their derivatives to realize excellent electrochemical performance.展开更多
Transition metal oxides(TMO) bring a novel direction for the development of energy store materials due to their excellent stability. They not only have high capacity and good cycle performance, but also are cheap and ...Transition metal oxides(TMO) bring a novel direction for the development of energy store materials due to their excellent stability. They not only have high capacity and good cycle performance, but also are cheap and easily available. Zinc oxide(Zn O) as an important part of TMO have gradually attracted attention in the research of electrochemistry. Zn O, as a metal semiconductor with the advantages of wide band gap, possesses high ion migration rate, good chemical stability, simple preparation and low cost, and is widely used in various fields. However, poor conductivity, low permittivity and quick capacity decays quickly impede the commercial application of these electrodes. In recent years, in order to improve the structural stability, ion diffusion and conductivity of zinc oxides-based anodes, various strategies have been raised, such as structural design, surface modification and composition control. In this paper, the recent advances of zinc oxides-based materials for batteries and hybrid supercapacitors(SCs) were introduced. We comprehensively reviewed the prepared process, reaction mechanism and electrochemical performance and discussed the shortcoming of zinc oxides-based nanomaterials. In particular, several insights toward the future research development, practical applications and commercialization of energy storage devices are also proposed for improving the performance of zinc oxides-based materials.展开更多
With the increasing popularity of new en ergy electric vehicles,the dema nd for lithium-ion batteries(LIBs)has been growing rapidly,which will produce a large number of spent LIBs.Therefore,recycling of spe nt LIBs ha...With the increasing popularity of new en ergy electric vehicles,the dema nd for lithium-ion batteries(LIBs)has been growing rapidly,which will produce a large number of spent LIBs.Therefore,recycling of spe nt LIBs has become an urge nt task to be solved,otherwise it will inevitably lead to serious environmental pollution.Herein,a unique recycling strategy is proposed to achieve the concurrent reuse of cathode and anode in the spent graphite/LiFePO_(4) batteries.Along with such recycling process,a unique cathode composed of recycled LFP/graphite(RLFPG)with cation/anion-co-storage ability is designed for new-type dual-ion battery(DIB).As a result,the recycle-derived DIB of Li/RLFPG is established with good electrochemical performance,such as an initial discharge capacity of 117.4 mA h g^(-1) at 25 mA g^(-1) and 78% capacity retention after 1000 cycles at 100 mA g^(-1).The working mechanism of Li/RLFPG DIB is also revealed via in situ X-ray diffraction and electrode kinetics studies.This work not only presents a farreaching significance for large-scale recycling of spent LIBs in the future,but also proposed a sustainable and econo mical method to design n ew-type sec on dary batteries as recycling of spe nt LIBs.展开更多
Joint time–frequency analysis is an emerging method for interpreting the underlying physics in fuel cells,batteries,and supercapacitors.To increase the reliability of time–frequency analysis,a theoretical correlatio...Joint time–frequency analysis is an emerging method for interpreting the underlying physics in fuel cells,batteries,and supercapacitors.To increase the reliability of time–frequency analysis,a theoretical correlation between frequency-domain stationary analysis and time-domain transient analysis is urgently required.The present work formularizes a thorough model reduction of fractional impedance spectra for electrochemical energy devices involving not only the model reduction from fractional-order models to integer-order models and from high-to low-order RC circuits but also insight into the evolution of the characteristic time constants during the whole reduction process.The following work has been carried out:(i)the model-reduction theory is addressed for typical Warburg elements and RC circuits based on the continued fraction expansion theory and the response error minimization technique,respectively;(ii)the order effect on the model reduction of typical Warburg elements is quantitatively evaluated by time–frequency analysis;(iii)the results of time–frequency analysis are confirmed to be useful to determine the reduction order in terms of the kinetic information needed to be captured;and(iv)the results of time–frequency analysis are validated for the model reduction of fractional impedance spectra for lithium-ion batteries,supercapacitors,and solid oxide fuel cells.In turn,the numerical validation has demonstrated the powerful function of the joint time–frequency analysis.The thorough model reduction of fractional impedance spectra addressed in the present work not only clarifies the relationship between time-domain transient analysis and frequency-domain stationary analysis but also enhances the reliability of the joint time–frequency analysis for electrochemical energy devices.展开更多
基金the financial support from:“Ministerio de Ciencia,Innovación y Universidades”of Spain(PID2021-127713OA-I00,PID2021-123511OB-C33,PID2021-124139NBC22-CIN/AEI/10.13039/501100011033/FEDER,EU,TED2021-129851B-I00-/AEI/10.13039/501100011033/Unión Europea NextGenerationEU/PRTR and RED2022-134219-T)“Ministerio da Educacao-MEC”of Brazil(CAPES PDPG-POSDOC 88887.807971/2023-00).
文摘The growing concern for energy efficiency and the increasing deployment of intermittent renewable energies has led to the development of technologies for capturing,storing,and discharging energy.Supercapacitors can be considered where batteries do not meet the requirements.However,supercapacitors in systems with a slower charge/discharge cycle,such as photovoltaic systems(PVS),present other obstacles that make replacing batteries more challenging.An extensive literature review unveils a knowledge gap regarding a methodological comparison of batteries and supercapacitors.In this study,we address the technological feasibility of intermittent renewable energy generation systems,focusing on storage solutions for PVS energy.We propose a framework according to one of the essential parameters for their application in PVS:Energy Density or Specific Energy(Wh/kg).Through computational modelling,issues related to the intermittency and seasonality of the solar energy source are addressed,evaluating the possible benefits of implementing batteries,supercapacitors,and hybrid solutions in renewable energy generation systems.Also,the characteristics of two hypothetical configurations of photovoltaic systems,off-grid and on-grid,were analysed.This analysis highlights the characteristics of totally isolated systems(e.g.,on an island or remote village)and systems connected to the grid(e.g.,solar farms),where eliminating the use of batteries can bring significant benefits,in addition to tax incentives,which are decisive in the investment decision-making process.The results clarify the viability of PVS and allow an understanding of parameters that can support the technical decision process between isolated or non-isolated systems,reflecting economic and financial issues.
文摘In order to meet the demands of new-generation electric vehicles that require high power output(over 15 kW/kg),it is crucial to increase the energy density of car-bon-based supercapacitors to a level comparable to that of batteries,while maintaining a high power density.We re-port a porous carbon material produced by immersing pop-lar wood(PW)sawdust in a solution of KOH and graphene oxide(GO),followed by carbonization.The resulting mater-ial has exceptional properties as an electrode for high-en-ergy supercapacitors.Compared to the material prepared by the direct carbonization of PW,its electrical conductivity was in-creased from 0.36 to 26.3 S/cm.Because of this and a high microporosity of over 80%,which provides fast electron channels and a large ion storage surface,when used as the electrodes for a symmetric supercapacitor,it gave a high energy density of 27.9 Wh/kg@0.95 kW/kg in an aqueous electrolyte of 1.0 mol/L Na_(2)SO_(4).The device also had battery-level energy storage with maximum energy densities of 73.9 Wh/kg@2.0 kW/kg and 67.6 Wh/kg@40 kW/kg,an ultrahigh power density,in an organic electrolyte of 1.0 mol/L TEABF4/AN.These values are comparable to those of 30−45 Wh/kg for Pb-acid batteries and 30−55 Wh/kg for aqueous lithium batteries.This work indicates a way to prepare carbon materials that can be used in supercapacit-ors with ultrahigh energy and power densities.
基金supported by the Australian Research Council Discovery Program(No.DP220103416)Australian Research Council Future Fellowships(Nos.FT200100730 and FT210100804)National Natural Science Foundation of China(Nos.52474431,51874051 and 52111530139).
文摘Herein,we developed three-dimensional pristine titanium dioxide(TiO_(2))photo-electrocatalyst material(PEM)with homogeneous distribution of oxygen vacancies(OV)for lithium-oxygen(Li-O_(2))battery system(denoted as LOBs)under illumination.This rationally designed OV-TiO_(2)photoelectrode-catalyst has exhibited excellent capacity,small overpotential,long-term cycle stability,and higher rate capability performance according to our electrochemical experiment study.In short,OV as photoinduced charge separation centers(inert surface atomic modification method)fascinate the effective separation of electrons(e^(−))and holes(h^(+)).In turn,induced e−and h+are beneficial to the oxygen reduction reaction(ORR)and oxygen evolution reaction(OER)process.More importantly,machine learning(ML)algorithms to analyze and optimize battery performance are innovative in the photoelectrical field.The utility of ML analysis is extensively shown to be effective in learning the in/output connection of interest.Based on ML analysis results,the OV-TiO_(2)cathode is indeed the key point to extend the LOB life span.More importantly,our brilliant anatase OV-TiO_(2)revealed the optimization of electrode material for high performance and reversibility in LOBs.We expect that it will bring special OV-TiO_(2)and some other hierarchical hollow nanomaterials,a big step toward battery technology no matter in cost-effectiveness and environmentally friendly aspects.
基金funded by the Bavarian State Ministry of Science,Research and Art(Grant number:H.2-F1116.WE/52/2)。
文摘In order to address the widespread data shortage problem in battery research,this paper proposes a generative adversarial network model that combines it with deep convolutional networks,the Wasserstein distance,and the gradient penalty to achieve data augmentation.To lower the threshold for implementing the proposed method,transfer learning is further introduced.The W-DC-GAN-GP-TL framework is thereby formed.This framework is evaluated on 3 different publicly available datasets to judge the quality of generated data.Through visual comparisons and the examination of two visualization methods(probability density function(PDF)and principal component analysis(PCA)),it is demonstrated that the generated data is hard to distinguish from the real data.The application of generated data for training a battery state model using transfer learning is further evaluated.Specifically,Bi-GRU-based and Transformer-based methods are implemented on 2 separate datasets for estimating state of health(SOH)and state of charge(SOC),respectively.The results indicate that the proposed framework demonstrates satisfactory performance in different scenarios:for the data replacement scenario,where real data are removed and replaced with generated data,the state estimator accuracy decreases only slightly;for the data enhancement scenario,the estimator accuracy is further improved.The estimation accuracy of SOH and SOC is as low as 0.69%and 0.58%root mean square error(RMSE)after applying the proposed framework.This framework provides a reliable method for enriching battery measurement data.It is a generalized framework capable of generating a variety of time series data.
基金support of the National Natural Science Foundation of China(22075131 and 22078265)the Shaanxi Fundamental Science Research Project for Mathematics and Physics under Grants(No.22JSZ005)the State-Key Laboratory of Multiphase Complex Systems(No.MPCS-2021-A).
文摘Lithium-sulfur(Li-S)batteries require efficient catalysts to accelerate polysulfide conversion and mitigate the shuttle effect.However,the rational design of catalysts remains challenging due to the lack of a systematic strategy that rationally optimizes electronic structures and mesoscale transport properties.In this work,we propose an autogenously transformed CoWO_(4)/WO_(2) heterojunction catalyst,integrating a strong polysulfide-adsorbing intercalation catalyst with a metallic-phase promoter for enhanced activity.CoWO_(4) effectively captures polysulfides,while the CoWO_(4)/WO_(2) interface facilitates their S-S bond activation on heterogenous catalytic sites.Benefiting from its directional intercalation channels,CoWO_(4) not only serves as a dynamic Li-ion reservoir but also provides continuous and direct pathways for rapid Li-ion transport.Such synergistic interactions across the heterojunction interfaces enhance the catalytic activity of the composite.As a result,the CoWO_(4)/WO_(2) heterostructure demonstrates significantly enhanced catalytic performance,delivering a high capacity of 1262 mAh g^(−1) at 0.1 C.Furthermore,its rate capability and high sulfur loading performance are markedly improved,surpassing the limitations of its single-component counterparts.This study provides new insights into the catalytic mechanisms governing Li-S chemistry and offers a promising strategy for the rational design of high-performance Li-S battery catalysts.
基金supported by the financial support from the National Research Foundation,Singapore,under its Singapore-China Joint Flagship Project(Clean Energy).
文摘Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from the cathode side.These challenges lead to poor cycle stability and severe self-discharge.From the fabrication and cost point of view,it is technologically more viable to deploy electrolyte engineering than electrode protection strategies.More importantly,a synchronous method for modulation of both cathode and anode is pivotal,which has been often neglected in prior studies.In this work,cationic poly(allylamine hydrochloride)(Pah^(+))is adopted as a low-cost dual-function electrolyte additive for ZIBs.We elaborate the synchronous effect by Pah^(+)in stabilizing Zn anode and immobilizing polyiodide anions.The fabricated Zn-iodine coin cell with Pah^(+)(ZnI_(2) loading:25 mg cm^(−2))stably cycles 1000 times at 1 C,and a single-layered 3.4 cm^(2) pouch cell(N/P ratio~1.5)with the same mass loading cycles over 300 times with insignificant capacity decay.
基金supported by the National Natural Science Foundation(52302284,22002086,22204096)Shanghai Sailing Program(23YF1412200)the Fundamental Research Funds for the Central Universities(22120240314).
文摘Single-atom catalysts(SACs)have garnered significant attention in lithium-sulfur(Li-S)batteries for their potential to mitigate the severe polysulfide shuttle effect and sluggish redox kinetics.However,the development of highly efficient SACs and a comprehensive understanding of their structure-activity relationships remain enormously challenging.Herein,a novel kind of Fe-based SAC featuring an asymmetric FeN_(5)-TeN_(4) coordination structure was precisely designed by introducing Te atom adjacent to the Fe active center to enhance the catalytic activity.Theoretical calculations reveal that the neighboring Te atom modulates the local coordination environment of the central Fe site,elevating the d-band center closer to the Fermi level and strengthening the d-p orbital hybridization between the catalyst and sulfur species,thereby immobilizing polysulfides and improving the bidirectional catalysis of Li-S redox.Consequently,the Fe-Te atom pair catalyst endows Li-S batteries with exceptional rate performance,achieving a high specific capacity of 735 mAh g^(−1) at 5 C,and remarkable cycling stability with a low decay rate of 0.038%per cycle over 1000 cycles at 1 C.This work provides fundamental insights into the electronic structure modulation of SACs and establishes a clear correlation between precisely engineered atomic configurations and their enhanced catalytic performance in Li-S electrochemistry.
基金supported by the National Nature Science Foundation of China(Nos.52202335 and 52171227)Natural Science Foundation of Jiangsu Province(No.BK20221137)National Key R&D Program of China(2024YFE0108500).
文摘Wide-temperature applications of sodium-ion batteries(SIBs)are severely limited by the sluggish ion insertion/diffusion kinetics of conversion-type anodes.Quantum-sized transition metal dichalcogenides possess unique advantages of charge delocalization and enrich uncoordinated electrons and short-range transfer kinetics,which are crucial to achieve rapid low-temperature charge transfer and high-temperature interface stability.Herein,a quantum-scale FeS_(2) loaded on three-dimensional Ti_(3)C_(2) MXene skeletons(FeS_(2) QD/MXene)fabricated as SIBs anode,demonstrating impressive performance under wide-temperature conditions(−35 to 65).The theoretical calculations combined with experimental characterization interprets that the unsaturated coordination edges of FeS_(2) QD can induce delocalized electronic regions,which reduces electrostatic potential and significantly facilitates efficient Na+diffusion across a broad temperature range.Moreover,the Ti_(3)C_(2) skeleton reinforces structural integrity via Fe-O-Ti bonding,while enabling excellent dispersion of FeS_(2) QD.As expected,FeS_(2) QD/MXene anode harvests capacities of 255.2 and 424.9 mAh g^(−1) at 0.1 A g^(−1) under−35 and 65,and the energy density of FeS_(2) QD/MXene//NVP full cell can reach to 162.4 Wh kg^(−1) at−35,highlighting its practical potential for wide-temperatures conditions.This work extends the uncoordinated regions induced by quantum-size effects for exceptional Na^(+)ion storage and diffusion performance at wide-temperatures environment.
基金supported by the National Natural Science Foundation of China(52002297)National Key R&D Program of China(2022VFB2404800)+1 种基金Wuhan Yellow Crane Talents Program,China Postdoctoral Science Foundation(No.2024M752495)the Postdoctoral Fellowship Program of CPSF(No.GZB20230552).
文摘Aqueous alkali metal-ion batteries(AAMIBs)have been recognized as emerging electrochemical energy storage technologies for grid-scale applications owning to their intrinsic safety,cost-effectiveness,and environmental sustainability.However,the practical application of AAMIBs is still severely constrained by the tendency of aqueous electrolytes to freeze at low temperatures and decompose at high temperatures,limiting their operational temperature range.Considering the urgent need for energy systems with higher adaptability and resilience at various application scenarios,designing novel electrolytes via structure modulation has increasingly emerged as a feasible and economical strategy for the performance optimization of wide-temperature AAMIBs.In this review,the latest advancement of wide-temperature electrolytes for AAMIBs is systematically and comprehensively summarized.Specifically,the key challenges,failure mechanisms,correlations between hydrogen bond behaviors and physicochemical properties,and thermodynamic and kinetic interpretations in aqueous electrolytes are discussed firstly.Additionally,we offer forward-looking insights and innovative design principles for developing aqueous electrolytes capable of operating across a broad temperature range.This review is expected to provide some guidance and reference for the rational design and regulation of widetemperature electrolytes for AAMIBs and promote their future development.
基金supported by the Fujian Provincial Science and Technology Planning Project(No.2022HZ027006,No.2024HZ021023)National Natural Science Foundation of China(No.U22A20118).
文摘High-entropy materials(HEMs)have attracted considerable research attention in battery applications due to exceptional properties such as remarkable structural stability,enhanced ionic conductivity,superior mechanical strength,and outstanding catalytic activity.These distinctive characteristics render HEMs highly suitable for various battery components,such as electrodes,electrolytes,and catalysts.This review systematically examines recent advances in the application of HEMs for energy storage,beginning with fundamental concepts,historical development,and key definitions.Three principal categories of HEMs,namely high-entropy alloys,high-entropy oxides,and highentropy MXenes,are analyzed with a focus on electrochemical performance metrics such as specific capacity,energy density,cycling stability,and rate capability.The underlying mechanisms by which these materials enhance battery performance are elucidated in the discussion.Furthermore,the pivotal role of machine learning in accelerating the discovery and optimization of novel high-entropy battery materials is highlighted.The review concludes by outlining future research directions and potential breakthroughs in HEM-based battery technologies.
基金supported by the National Key R&D Program of China(No.2023YFB3809500)the Fundamental Research Funds for the Central Universities(No.2024CDJXY003)+1 种基金the Venture&Innovation Support Program for Chongqing Overseas Returnees(cx2023087)The Chongqing Technology Innovation and Application Development Project(No.2024TIAD-KPX0003).
文摘Micro-sized anatase TiO_(2) displays inferior capacity as cathode material for magnesium ion batteries because of the higher diffusion energy barrier of Mg^(2+)in anatase TiO_(2) lattice.Herein,we report that nanosized anatase TiO_(2) exposed(001)facet doubles the capacity compared to the micro-sized sample ascribed to the interfacial Mg^(2+)ion storage.First-principles calculations reveal that the diffusion energy barrier of Mg^(2+)on the(001)facet is significantly lower than those in the bulk phase and on(100)facet,and the adsorption energy of Mg^(2+)on the(001)facet is also considerably lower than that on(100)facet,which guarantees superior interfacial Mg^(2+)storage of(001)facet.Moreover,anatase TiO_(2) exposed(001)facet displays a significantly higher capacity of 312.9 mAh g^(−1) in Mg-Li dual-salt electrolyte compared to 234.3 mAh g^(−1) in Li salt electrolyte.The adsorption energies of Mg^(2+)on(001)facet are much lower than the adsorption energies of Li+on(001)facet,implying that the Mg^(2+)ion interfacial storage is more favorable.These results highlight that controlling the crystal facet of the nanocrystals effectively enhances the interfacial storage of multivalent ions.This work offers valuable guidance for the rational design of high-capacity storage systems.
基金financial support from NSFC(51602332)the National Key Research and Development Program of China(2016YFB0700204)+4 种基金Science and Technology Commission of Shanghai Municipality(15520720400,16DZ2260603)Equipment Research Program(6140721050215)the National 1000 Youth Talents program of Chinafinancial support from Ningbo 3315 programDST Solar Energy Harnessing Centre(DST/TMD/SERI/HUB/1(C)),DST Materials for Energy Storage program,Ministry of Electronics and Information Technology(India)(Project ID:ELE1819353MEITNAK)
文摘Nitrogen-doped carbon materials with a large specific surface area,high conductivity,and adjustable microstructures have many prospects for energy-related applications.This is especially true for N-doped nanocarbons used in the electrocatalytic oxygen reduction reaction(ORR)and supercapacitors.Here,we report a low-cost,environmentally friendly,large-scale mechanochemical method of preparing N-doped porous carbons(NPCs)with hierarchical micro-mesopores and a large surface area via ball-milling polymerization followed by pyrolysis.The optimized NPC prepared at 1000°C(NPC-1000)offers excellent ORR activity with an onset potential(Eonset)and half-wave potential(E1/2)of 0.9 and 0.82 V,respectively(vs.a reversible hydrogen electrode),which are only approximately 30 mV lower than that of Pt/C.The rechargeable Zn–air battery assembled using NPC-1000 and the NiFe-layered double hydroxide as bifunctional ORR and oxygen evolution reaction electrodes offered superior cycling stability and comparable discharge performance to RuO2 and Pt/C.Moreover,the supercapacitor electrode equipped with NPC prepared at 800℃ exhibited a high specific capacity(431 F g^−1 at 10 mV s^−1),outstanding rate,performance,and excellent cycling stability in an aqueous 6-M KOH solution.This work demonstrates the potential of the mechanochemical preparation method of porous carbons,which are important for energy conversion and storage.
基金the support received from National Natural Science Foundation of China(Grant No.22109012)the Beijing Municipal Natural Science Foundation(Grant No.2212052)the Fundamental Research Funds for the Central Universities(Grant No.E1E46805).
文摘Lightweight and flexible self-charging power systems with synchronous energy harvesting and energy storage abilities are highly desired in the era of the internet of things and artificial intelligences,which can provide stable,sustainable,and autonomous power sources for ubiquitous,distributed,and low-power wearable electronics.However,there is a lack of comprehensive review and challenging discussion on the state-of-the-art of the triboelectric nanogenetor(TENG)-based self-charging power textiles,which have a great possibility to become the future energy autonomy power sources.Herein,the recent progress of the self-charging power textiles hybridizing fiber/fabric based TENGs and fiber/fabric shaped batteries/supercapacitors is comprehensively summarized from the aspect of textile structural designs.Based on the current research status,the key bottlenecks and brighter prospects of self-charging power textiles are also discussed in the end.It is hoped that the summary and prospect of the latest research of self-charging power textiles can help relevant researchers accurately grasp the research progress,focus on the key scientific and technological issues,and promote further research and practical application process.
基金supported by the National Natural Science Foundation of China (grant no. 51672151).
文摘Lithium-ion hybrid supercapacitors(Li-HSCs) and dual-ion batteries(DIBs) are two types of energy storage devices that have attracted extensive research interest in recent years. Li-HSCs and DIBs have similarities in device structure, tendency for ion migration, and energy storage mechanisms at the negative electrode. However, these devices have differences in energy storage mechanisms and working potentials at the positive electrode. Here, we first realize the integration of a Li-HSC and a DIB to form a dual-ion hybrid supercapacitor(DIHSC), by employing mesocarbon microbead(MCMB)-based porous graphitic carbon(PGC) with a partially graphitized structure and porous structure as a positive electrode material. The MCMB-PGC-based DIHSC exhibits a novel dual-ion battery-capacitor hybrid mechanism: it exhibits excellent electronic double-layer capacitor(EDLC) behavior like a Li-HSC in the low-middle wide potential range and anion intercalation/de-intercalation behavior like a DIB in the high-potential range. Two types of mechanisms are observed in the electrochemical characterization process, and the energy density of the new DIHSC is significantly increased.
文摘A novel process is reported which produces an asymmetric supercapacitor through the complete recycling of end-of-life lithium ion batteries.The electrodic powder recovered by industrial scale mechanical treatment of spent batteries was leached and the dissolved metals were precipitated as mixed metals carbonates.Nanowires battery-type positive electrodes were produced by electrodeposition into nanoporous alumina templates from the electrolytic baths prepared by dissolution of the precipitated carbonates.The impact of the different metals contained in the electrodic powder was evaluated by benchmarking the electrochemical performances of the recovered nanowires-based electrodes against electrodes produced by using high-purity salts.Presence of inactive Cu in the nanowires lowered the final capacitance of the electrodes while Ni showed a synergistic effect with cobalt providing a higher capacitance with respect to synthetic Co electrodes.The carbonaceous solid recovered after leaching was indepth characterized and tested as negative electrode.Both the chemical and electrochemical characterization indicate that the recovered graphite is characterized by the presence of oxygen functionalities introduced by the leaching treatment.This has led to the obtainment of a recovered graphite characterized by an XPS C/O ratio,Raman spectrum and morphology close to literature reports for reduced graphene oxide.The asymmetric supercapacitor assembled using the recovered nanowires-based positive electrodes and graphite as negative electrodes has shown a specific capacitance of 42 F g^(-1), computed including the whole weight of the positive electrode and recovered graphite,providing a maximum energy density of ~9 Wh kg^(-1) and a power density of 416 W kg^(-1) at 2.5 mA cm^(-2).
基金financially supported by National Natural Science Foundation of China (No. 51672083)Program of Shanghai Academic/Technology Research Leader (18XD1401400)+3 种基金Basic Research Program of Shanghai (17JC1404702)Leading talents in Shanghai in 2018The 111 project (B14018)the Fundamental Research Funds for the Central Universities (222201718002)
文摘As promising energy storage systems,lithium-sulfur(Li-S)batteries have attracted significant attention because of their ultra-high energy densities.However,Li-S battery suffers problems related to the complex phase conversion that occurs during the charge-discharge process,particularly the deposition of solid Li2S from the liquid-phase polysulfides,which greatly limits its practical application.In this paper,edge-rich MoS2/C hollow microspheres(Edg-MoS2/C HMs)were designed and used to functionalize separator for Li-S battery,resulting in the uniform deposition of Li2S.The microspheres were fabricated through the facile hydrothermal treatment of MoO3-aniline nanowires and a subsequent carbonization process.The obtained Edg-MoS2/C HMs have a strong chemical absorption capability and high density of Li2S binding sites,and exhibit excellent electrocatalytic performance and can effectively hinder the polysulfide shuttle effect and guide the uniform nucleation and growth of Li2S.Furthermore,we demonstrate that the Edg-MoS2/C HMs can effectively regulate the deposition of Li2S and significantly improve the reversibility of the phase conversion of the active sulfur species,especially at high sulfur loadings and high C-rates.As a result,a cell containing a separator functionalized with Edg-MoS2/C HMs exhibited an initial discharge capacity of 935 mAh g-1 at 1.0 C and maintained a capacity of 494 mAh g-1 after 1000 cycles with a sulfur loading of 1.7 mg cm-2.Impressively,at a high sulfur loading of 6.1 mg cm-2 and high rate of 0.5 C,the cell still delivered a high reversible discharge capacity of 478 mAh g-1 after 300 cycles.This work provides fresh insights into energy storage systems related to complex phase conversions.
基金supported by the National Natural Science Foundation of China (Nos. NSFC-U1904215)the Top-notch Academic Programs Project of Jiangsu Higher Education Institutions (TAPP)+2 种基金the Natural Science Foundation of Jiangsu Province (No. BK20200044)Program for Young Changjiang Scholars of the Ministry of Education,China (No. Q2018270)the Priority Academic Program Development of Jiangsu Higher Education Institutions
文摘Metal–organic frameworks(MOFs),which are generally considered to be crystalline materials comprising metal centers and organic ligands,have attracted growing attention because of their controllable structures and high porosity.MOFs based on transition metals(Fe,Co,Ni)are highly effi cient electrode materials for electrochemical energy storage.In this review,the characteristics of Fe-MOFs,Co-MOFs,Ni-MOFs,and their derivatives are summarized,and the relationships between the structures and performance are unveiled in depth.Additionally,their applications in lithium–ion batteries,lithium–sulfur batteries,and supercapacitors are discussed.This review sheds light on the development of MOFs and their derivatives to realize excellent electrochemical performance.
基金financially supported by the National Natural Science Foundation of China (Nos.U1960107 and 51774002)the “333 Talent Project of Hebei Province (No.A202005018)the Fundamental Research Funds for the Central Universities (Nos.N2123034 and N2123001)。
文摘Transition metal oxides(TMO) bring a novel direction for the development of energy store materials due to their excellent stability. They not only have high capacity and good cycle performance, but also are cheap and easily available. Zinc oxide(Zn O) as an important part of TMO have gradually attracted attention in the research of electrochemistry. Zn O, as a metal semiconductor with the advantages of wide band gap, possesses high ion migration rate, good chemical stability, simple preparation and low cost, and is widely used in various fields. However, poor conductivity, low permittivity and quick capacity decays quickly impede the commercial application of these electrodes. In recent years, in order to improve the structural stability, ion diffusion and conductivity of zinc oxides-based anodes, various strategies have been raised, such as structural design, surface modification and composition control. In this paper, the recent advances of zinc oxides-based materials for batteries and hybrid supercapacitors(SCs) were introduced. We comprehensively reviewed the prepared process, reaction mechanism and electrochemical performance and discussed the shortcoming of zinc oxides-based nanomaterials. In particular, several insights toward the future research development, practical applications and commercialization of energy storage devices are also proposed for improving the performance of zinc oxides-based materials.
基金support from the National Natural Science Foundation of China(No.91963118)the Science Technology Program of Jilin Province(No.20200201066JC)the 111 Project(No.B13013).
文摘With the increasing popularity of new en ergy electric vehicles,the dema nd for lithium-ion batteries(LIBs)has been growing rapidly,which will produce a large number of spent LIBs.Therefore,recycling of spe nt LIBs has become an urge nt task to be solved,otherwise it will inevitably lead to serious environmental pollution.Herein,a unique recycling strategy is proposed to achieve the concurrent reuse of cathode and anode in the spent graphite/LiFePO_(4) batteries.Along with such recycling process,a unique cathode composed of recycled LFP/graphite(RLFPG)with cation/anion-co-storage ability is designed for new-type dual-ion battery(DIB).As a result,the recycle-derived DIB of Li/RLFPG is established with good electrochemical performance,such as an initial discharge capacity of 117.4 mA h g^(-1) at 25 mA g^(-1) and 78% capacity retention after 1000 cycles at 100 mA g^(-1).The working mechanism of Li/RLFPG DIB is also revealed via in situ X-ray diffraction and electrode kinetics studies.This work not only presents a farreaching significance for large-scale recycling of spent LIBs in the future,but also proposed a sustainable and econo mical method to design n ew-type sec on dary batteries as recycling of spe nt LIBs.
基金support from the National Science Foundation of China(22078190)the National Key R&D Plan of China(2020YFB1505802).
文摘Joint time–frequency analysis is an emerging method for interpreting the underlying physics in fuel cells,batteries,and supercapacitors.To increase the reliability of time–frequency analysis,a theoretical correlation between frequency-domain stationary analysis and time-domain transient analysis is urgently required.The present work formularizes a thorough model reduction of fractional impedance spectra for electrochemical energy devices involving not only the model reduction from fractional-order models to integer-order models and from high-to low-order RC circuits but also insight into the evolution of the characteristic time constants during the whole reduction process.The following work has been carried out:(i)the model-reduction theory is addressed for typical Warburg elements and RC circuits based on the continued fraction expansion theory and the response error minimization technique,respectively;(ii)the order effect on the model reduction of typical Warburg elements is quantitatively evaluated by time–frequency analysis;(iii)the results of time–frequency analysis are confirmed to be useful to determine the reduction order in terms of the kinetic information needed to be captured;and(iv)the results of time–frequency analysis are validated for the model reduction of fractional impedance spectra for lithium-ion batteries,supercapacitors,and solid oxide fuel cells.In turn,the numerical validation has demonstrated the powerful function of the joint time–frequency analysis.The thorough model reduction of fractional impedance spectra addressed in the present work not only clarifies the relationship between time-domain transient analysis and frequency-domain stationary analysis but also enhances the reliability of the joint time–frequency analysis for electrochemical energy devices.
