FeS_(2)is a promising anode material for potassium-ion batteries(PIBs),with the advantages of low cost and high capacity.However,it still faces challenges of capacity fading and poor rate performance in potassium stor...FeS_(2)is a promising anode material for potassium-ion batteries(PIBs),with the advantages of low cost and high capacity.However,it still faces challenges of capacity fading and poor rate performance in potassium storage.Rational structural design is one way to overcome these drawbacks.In this work,MIL-88B-Fe-derived FeS_(2)nanoparticles/N-doped carbon nanofibers(M-FeS_(2)@CNFs)with expansion buffer capability are designed and synthesized for high-performance PIB anodes via electrospinning and subsequent sulfurization.The uniformly distributed cavity-type porous structure effectively mitigates the severe aggregation problem of FeS_(2)nanoparticles during cycling and buffers the volume change,further enhancing the potassium storage capacity.Meanwhile,the robust KF-rich solid electrolyte interphase induced by methyl trifluoroethylene carbonate(FEMC)additive improves the cycling stability of the M-FeS_(2)@CNF anode.In the electrolyte with 3 wt%FEMC,the M-FeS_(2)@CNF anode shows a reversible specific capacity of 592.7 mA h g^(-1)at 0.1 A g^(-1),an excellent rate capability of 327.1 mA h g^(-1)at 5 A g^(-1),and a retention rate 80.7%over 1000 cycles at 1 A g^(-1).More importantly,when assembled with a K_(1.84)Ni[Fe(CN)_(6)]_(0.88)·0.49H_(2)O cathode,the full battery manifests excellent cycle stability and high rate performance.This study demonstrates the significant importance of the synergistic effect of structural regulation and electrolyte optimization in achieving high cycling stability of PIBs.展开更多
The distinguishing feature of Fe_(3)GeTe_(2)lies in its robu st in-plane chemical bonds within layers,which are interconnected by the weak van der Waals forces between adjacent layers,offering a stable framework chara...The distinguishing feature of Fe_(3)GeTe_(2)lies in its robu st in-plane chemical bonds within layers,which are interconnected by the weak van der Waals forces between adjacent layers,offering a stable framework characterized by enhanced interlayer spacing,thereby facilitating the migration of large-sized alkali metal ions.However,to date,there have been no reported studies on the ion storage performance of Fe_(3)GeTe_(2).In this study,Fe_(3)GeTe_(2)is synthesized via the chemical vapor transport method to assess its sodium/potassium storage capabilities.Fe_(3)GeTe_(2)is characterized by its impressive conductivity,a distinctive layered architecture,and a notably wide interlayer spacing,all of these attributes collectively contributing to its superior ion storage proficiency in both sodium-ion batteries(SIBs)and potassiumion batteries(PIBs).Specifically,it demonstrates exceptional electrochemical performance,maintaining a capacity of 291.8 mA h g^(-1)at 5 A g^(-1)in SIBs and 125.0 mA h g^(-1)over 6000 cycles at 3 A g^(-1)in PIBs.A series of in/ex situ characterizations uncover the reaction mechanism of Fe_(3)GeTe_(2)in the both systems,involving a combined process of intercalation,conversion,and alloying.Theoretical calculations provide further insights into the high ion adsorption affinity and diffusion kinetics of Fe_(3)GeTe_(2)in these systems.Analytical findings reveal its superior electrochemical performance in SIBs compared to PIBs,owing to higher diffusion kinetics and reactivity.This research establishes both experimental evidence and theoretical underpinnings for the utilization of Fe_(3)GeTe_(2)in SIBs and PIBs,opening up a new avenue for the utilization of germanium-based ternary materials in the field of energy storage.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
Transition metal selenides are considered promising electrochemical energy storage materials due to their excellent rate properties and high capacity based on multi-step conversion reactions.However,its practical appl...Transition metal selenides are considered promising electrochemical energy storage materials due to their excellent rate properties and high capacity based on multi-step conversion reactions.However,its practical applications are hampered by poor conductivity and large volume variation for Na^(+)storage,which resulting fast capacity decay.Herein,a facile metal-organic framework(MOF)derived method is explored to embed Cu_(2-x)Se@C particles into a carbon nanobelts matrix.Such carbon encapsulated nanobelts'structural moderate integral electronic conductivity and maintained the structure from collapsing during Na^(+)insertion/extraction.Furthermore,the porous structure of these nanobelts endows enough void space to mitigate volume stress and provide more diffusion channels for Na^(+)/electrons transporting.Due to the unique structure,these Cu_(2-x)Se@C nanobelts achieved ultra-stable cycling performance(170.7 m Ah/g at1.0 A/g after 1000 cycles)and superior rate capability(94.6 m Ah/g at 8 A/g)for sodium-ion batteries.The kinetic analysis reveals that these Cu_(2-x)Se@C nanobelts with considerable pesoudecapactive contribution benefit the rapid sodiation/desodiation.This rational design strategy broadens an avenue for the development of metal selenide materials for energy storage devices.展开更多
Aqueous zinc-ion batteries(ZIBs)are promising candidates for next-generation energy storage,but the problems related to Zn dendrites and side reactions severely hinder their practical applications.Herein,a self-recogn...Aqueous zinc-ion batteries(ZIBs)are promising candidates for next-generation energy storage,but the problems related to Zn dendrites and side reactions severely hinder their practical applications.Herein,a self-recognition separator based on a Bi-based metal-organic framework(GF@CAU-17)is developed for ion management to achieve highly reversible Zn anodes.The GF@CAU-17 has self-recognition behavior to customize selective Zn^(2+)channels,effectively repelling SO_(4)^(2-)and H_(2)O,but facilitating Zn^(2+)conduction.The inherent properties of CAU-17 result in the repulsion of SO_(4)^(2-)ions while disrupting the hydrogen bond network among free H_(2)O molecules,restraining side reactions and by-products.Simultaneously,the zincophilic characteristic of CAU-17 expedites the desolvation of[Zn(H_(2)O)6]^(2+),leading to a self-expedited Zn^(2+)ion pumping effect that dynamically produces a steady and homogeneous Zn^(2+)ion flux,and thereby alleviates concentration polarization.Consequently,a symmetric cell based on the GF@CAU-17 separator can achieve a long lifespan of 4450 h.Moreover,the constructed Zn//GF@CAU-17//MnO_(2)cell delivers a high specific capacity of 221.8 mAh g^(-1)and 88.0%capacity retention after 2000 cycles.展开更多
SnO_(2)-based anodes for lithium-ion batteries(LIBs)experience volume expansion,leading to rapid capacity decay and low conductivity.To address this problem,a composite consists of C/SnO_(2) with a core-shell structur...SnO_(2)-based anodes for lithium-ion batteries(LIBs)experience volume expansion,leading to rapid capacity decay and low conductivity.To address this problem,a composite consists of C/SnO_(2) with a core-shell structure and a carbonized nitrogen-doped Co-metal organic framework(Co-MOF)(NC)supported on carbon cloth(CC)was designed and prepared,which was denoted as C/SnO_(2)@NC@CC.C/SnO_(2)@NC@CC could be used directly as a flexible anode for LIBs.The combination of core-shell structure centered on carbon spheres,carbonized nitrogen-doped Co-MOF,and CC not only restricts the volume expansion but also functions as conductive networks to improve the electrical conductivity.C/SnO_(2)@NC@CC exhibits excellent electrochemical performance with charge and discharge specific capacities of 2066.0 and 2077.1 mAh/g,respectively,after 120 cycles at a current density of 0.5 A/g.展开更多
This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated thro...This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated through an innovative strategy involving Sn electrodeposition,oxidation,and MnO_(2)-layer preparation.The structure of the anode was characterized,and the oxygen evolution performance was evaluated in a H_(2)SO_(4) solution.The results show that compared with the Ti/SnO_(2)/MnO_(2) anode prepared by the conventional brushing-annealing process,the Ti/SnO_(x)/MnO_(2) anode fabricated through the innovative procedure exhibits a lower oxygen evolution potential and a nearly 40%longer accelerated lifespan.The superior oxygen evolution performance of the Ti/SnO_(x)/MnO_(2) anode is attributed to the distinctive SnO_(x) intermediate layer fabricated through Sn electrodeposition followed by oxidation,which indicates the great potential of the anode as a dimensionally stable anode for metal electrowinning and hydrogen production by electrolysis,etc.展开更多
Conversion-type anode materials are highly desirable for Na-ion batteries(NIBs)due to their high theoretical capacity.Nevertheless,the active materials undergo severe expansion and pulverization during the sodiation,r...Conversion-type anode materials are highly desirable for Na-ion batteries(NIBs)due to their high theoretical capacity.Nevertheless,the active materials undergo severe expansion and pulverization during the sodiation,resulting in inferior cycling stability.Herein,a self-supporting three-dimensional(3D)graphene sponge decorated with Fe_(2)O_(3)nanocubes(rGO@Fe_(2)O_(3))is constructed.Specifically,the 3D graphene sponge with resilience and high porosity benefits to accommodate the volume expansion of the Fe_(2)O_(3)nanocubes and facilitates the rapid electrons/ions transport,enabling spatial confinement to achieve outstanding results.Besides,the free-standing rGO@Fe_(2)O_(3)can be directly used as an electrode without additional binders and conductive additives,which helps to obtain a higher energy density.Based on the total mass of the rGO@Fe_(2)O_(3)material,the rGO@Fe_(2)O_(3)anode presents a specific capacity of 859 mAh/g at 0.1 A/g.It also delivers an impressive cycling performance(327 mAh/g after 2000 cycles at 1 A/g)and a superior rate capacity(162mAh/g at 20 A/g).The coin-type Na_(3)V_(2)(PO_(4))_(3)@C//rGO@Fe_(2)O_(3)NIB exhibits an energy density of 265.3Wh/kg.This unique 3D ionic/electronic conductive network may provide new strategies to design advanced conversion-type anode materials for high-performance NIBs.展开更多
In sulfide-based all-solid-state lithium batteries(ASLBs),the development of high-capacity anode materials with stable interfaces to sulfide solid-state electrolytes(SSEs)is critical.Here,In_(2)O_(3)is explored as an ...In sulfide-based all-solid-state lithium batteries(ASLBs),the development of high-capacity anode materials with stable interfaces to sulfide solid-state electrolytes(SSEs)is critical.Here,In_(2)O_(3)is explored as an anode material for ASLBs for the first time,demonstrating exceptional interfacial stability and electrochemical performance.The In_(2)O_(3)anode,with a substantial mass loading of 7.64 mg cm^(-2),sustains a charge-specific capacity of528.0 mAh g^(-1)(4.03 mAh cm^(-2))at a current density of0.76 mA cm^(-2)over 500 cycles,with a capacity retention of 81.2%.Additionally,it exhibits remarkable long-term cycling stability(2900 cycles)under a high current density of 3.82 mA cm^(-2),with an exceptionally low decay rate of0.016%per cycle.The charge-discharge mechanism of the In_(2)O_(3)anode is elucidated in detail,revealing that the electrochemical evolution of In_(2)O_(3)in ASLBs involves notonly the alloying/dealloying process of indium(In)but also a conversion reaction between In and Li_(2)O.Notably,as cycling progresses,the conversion reaction of In and Li_(2)O diminishes,with the reversible alloy ing/dealloy ing process becoming predominant.This work offers valuable insights for advancing oxide anode materials in sulfide-based ASLBs.展开更多
Aqueous zinc-ion batteries (AZIBs) are fundamentally challenged by the instability of the electrode/electrolyte interface,predominantly due to irreversible zinc (Zn) deposition and hydrogen evolution.Particularly,the ...Aqueous zinc-ion batteries (AZIBs) are fundamentally challenged by the instability of the electrode/electrolyte interface,predominantly due to irreversible zinc (Zn) deposition and hydrogen evolution.Particularly,the intricate mechanisms behind the electrochemical discrepancies induced by interfacial Zn^(2+)-solvation and deposition behavior demand comprehensive investigation.Organic molecules endowed with special functional groups (such as hydroxyl,carboxyl,etc.) have the potential to significantly optimize the solvation structure of Zn^(2+)and regulate the interfacial electric double layer (EDL).By increasing nucleation overpotential and decreasing interfacial free energy,these functional groups facilitate a lower critical nucleation radius,thereby forming an asymptotic nucleation model to promote uniform Zn deposition.Herein,this study presents a pioneering approach by introducing trace amounts of n-butanol as solvation regulators to engineer the homogenized Zn (H-Zn) anode with a uniform and dense structure.The interfacial reaction and structure evolution are explored by in/ex-situ experimental techniques,indicating that the H-Zn anode exhibits dendrite-free growth,no by-products,and weak hydrogen evolution,in sharp contrast to the bare Zn.Consequently,the H-Zn anode achieves a remarkable Zn utilization rate of approximately 20% and simultaneously sustains a prolonged cycle life exceeding 500 h.Moreover,the H-Zn//NH_(4)V_(4)O^(10)(NVO) full battery showcases exceptional cycle stability,retaining 95.04%capacity retention after 400 cycles at a large current density of 5 A g^(-1).This study enlightens solvation-regulated additives to develop Zn anode with superior utilization efficiency and extended operational lifespan.展开更多
Pb?Ag?PbO2 composite anodes with different mass fractions(1%,2%,3%,4%and 5%)ofβ-PbO2 were prepared by powder-pressed(PP)method.The galvanostatic polarization curves,Tafel curves and anodic polarization curves were te...Pb?Ag?PbO2 composite anodes with different mass fractions(1%,2%,3%,4%and 5%)ofβ-PbO2 were prepared by powder-pressed(PP)method.The galvanostatic polarization curves,Tafel curves and anodic polarization curves were tested in sulfuric acid solution.The morphologies and phase compositions of the anodic layers formed after galvanostatic polarization were investigated by using scanning electron microscope(SEM)and X-ray diffractometer(XRD),respectively.The results showed thatβ-PbO2 can improve the electrocatalytic activity of anodic oxide.The anode containing 3%β-PbO2 had the lowest overpotential of oxygen evolution reaction(OER)and the best corrosion resistance.The morphologies of the anode surfaces were gradually transformed from regular crystals to amorphous ones as the content ofβ-PbO2 increased in anodes.展开更多
A comparative study on the corrosion resistance of 17Ni/（NiFe2O4-10NiO） cermet inert anode prepared in differentsintering atmospheres was conducted in Na3AlF6-Al2O3 melt. The results indicate that the corrosion rate...A comparative study on the corrosion resistance of 17Ni/（NiFe2O4-10NiO） cermet inert anode prepared in differentsintering atmospheres was conducted in Na3AlF6-Al2O3 melt. The results indicate that the corrosion rates of NiFe2O4-based cermetanodes prepared in the vacuum and the atmosphere with oxygen content of 2×10^-3 （volume fraction） are 6.46 and 2.71 cm/a,respectively. Though there is a transition layer with lots of holes or pores, a densified layer is formed on the surface of anode due tosome reactions producing aluminates. For the anode prepared in the atmosphere with oxygen content of 2×10^-3, the thickness of thedensification layer （about 50 μm） is thicker than that （about 30 μm） formed on the surface of anode prepared in the vacuum. Thecontents of NiO and Fe（II） in NiFe2xO4-y-z increase with the decrease of oxygen content in sintering atmosphere, which reduces thecorrosion resistance of the material.展开更多
NiFe2O4-10NiO-based cermet inert anodes for aluminium electrolysis were prepared and their properties were investigated in a lab-scale electrolysis cell. The results show that the inert anodes exhibit good performance...NiFe2O4-10NiO-based cermet inert anodes for aluminium electrolysis were prepared and their properties were investigated in a lab-scale electrolysis cell. The results show that the inert anodes exhibit good performance during electrolysis in molten salt cryolite at 960 °C, but according to the analyses of phase compositions and microstructures through XRD, SEM/EDX and metallographic analysis, the metal in the anodes is preferentially corroded and many pores are produced on the anode surface after electrolysis. The preferential dissolution of Fe in the NiFe2O4 phase may lead to the non-uniform corrosion of NiFe2O4 grains. Moreover, a dense protective layer of NiFe2O4-NiAl2O4-FeAl2O4 is formed on the anode surface, which originates from the reaction of Al2O3 dissolved in the electrolyte with NiO or FeO, the annexation of NiFe2O4-NiAl2O4-FeAl2O4 to NiO and volume expansion. Thus, the dense NiFe2O4-NiAl2O4-FeAl2O4 layer inhibits the metal loss and ceramic-phase corrosion on the surface of the cermet inert anodes.展开更多
A novel SnO2-based gas anode was developed for aluminum electrolysis in molten cryolite at 850 ＆#176;C to reduce energy consumption and decrease CO2 emissions. Hydrogen was introduced into the anode, participating in...A novel SnO2-based gas anode was developed for aluminum electrolysis in molten cryolite at 850 ＆#176;C to reduce energy consumption and decrease CO2 emissions. Hydrogen was introduced into the anode, participating in the anode reaction. Carbon and aluminum were used as the cathode and reference electrodes, respectively. Cyclic voltammetry was applied in the cell to investigate the electrochemical behavior of oxygen ion on platinum and SnO2-based materials. The potential for oxygen evolution on these electrode materials was determined. Then, galvanostatic electrolysis was performed on the gas anode, showing a significant depolarization effect （a decrease of ~0.8 V of the anode potential） after the introduction of hydrogen, compared with no gas introduction or the introduction of argon. The results indicate the involvement of hydrogen in the anode reaction （three-phase-boundary reaction including gas, electrolyte and electrode） and give the possibility for the utilization of reducing gas anodes for aluminum electrolysis.展开更多
It is urgent to solve the problems of the dramatic volume expansion and pulverization of SnO_2 anodes during cycling process in battery systems. To address this issue, we design a hybrid structure of N-doped carbon fi...It is urgent to solve the problems of the dramatic volume expansion and pulverization of SnO_2 anodes during cycling process in battery systems. To address this issue, we design a hybrid structure of N-doped carbon fibers@SnO_2 nanoflowers(NC@SnO_2) to overcome it in this work. The hybrid NC@SnO_2 is synthesized through the hydrothermal growth of SnO_2 nanoflowers on the surface of N-doped carbon fibers obtained by electrospinning. The NC is introduced not only to provide a support framework in guiding the growth of the SnO_2 nanoflowers and prevent the flower-like structures from agglomeration, but also serve as a conductive network to accelerate electronic transmission along one-dimensional structure effectively. When the hybrid NC@SnO_2 was served as anode, it exhibits a high discharge capacity of 750 Ah g^(-1) at 1 A g^(-1) after 100 cycles in Li-ion battery and 270 mAh g^(-1) at 100 mA g^(-1) for 100 cycles in Na-ion battery, respectively.展开更多
Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion di usion k...Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion di usion kinetics. An SnS_2@carbon hollow nanospheres(SnS_2@C) has been designed and fabricated via a facile solvothermal route, followed by an annealing treatment. The SnS_2@C hybrid possesses an ideal hollow structure, rich active sites, a large electrode/electrolyte interface, a shortened ion transport pathway, and, importantly, a bu er space for volume change, generated from the repeated insertion/extraction of sodium ions. These merits lead to the significant reinforcement of structural integrity during electrochemical reactions and the improvement in sodium storage properties, with a high specific reversible capacity of 626.8 mAh g^(-1) after 200 cycles at a current density of 0.2 A g^(-1) and superior high-rate performance(304.4 mAh g^(-1) at 5 A g^(-1)).展开更多
Sodium-ion batteries(SIBs)have attracted significant attention with respect to renewable energy power generation systems because of the abundant reserves of sodium on earth.However,anode materials are presently limite...Sodium-ion batteries(SIBs)have attracted significant attention with respect to renewable energy power generation systems because of the abundant reserves of sodium on earth.However,anode materials are presently limited by low energy density,poor rate performance and inferior cycling stability.In recent years,tin disulfide(SnS_(2))with a particular layered structure has been considered as a promising anode material for SIBs due to its high theoretical capacity and low cost.Herein,a nervoussystem-like structured SnS_(2)/CNTs composite was successfully synthesized via a hydrothermal method.The SnS_(2)sheets were strung with carbon nanotubes(CNTs)to form a hierarchical porous structure,which is effective for electrolyte diffusion and electronic transmission.The large distance of the(001)plane(0.5899 nm)of SnS_(2)favors Na+insertion-extraction dynamics.Benefitting from these structural characteristics,SnS_(2)/CNTs electrodes exhibit high specific capacity,excellent rate performance and superior cycling stability.A high charge capacity of 642 mAh·g^(-1)was released at 0.2 A·g^(-1),and then,a high reversible capacity of 427 mAh·g^(-1)was retained after 100 cycles.Even charged at 2 A·g^(-1),the SnS_(2)/CNTS electrode maintained a capacity of 282 mAh·g^(-1).The nervous-system-like structure of the SnS_(2)/CNTs composite provides a novel strategy for the development of SIBs with high electrochemical performance.展开更多
Self-organized titanium dioxide(TiO_(2))nanotubes,which are prepared by electrochemical anodizing,have been widely researched as promising anodes for Liion batteries.Both nanotubular morphology and bulk structure of T...Self-organized titanium dioxide(TiO_(2))nanotubes,which are prepared by electrochemical anodizing,have been widely researched as promising anodes for Liion batteries.Both nanotubular morphology and bulk structure of TiO_(2)nanotubes can be easily changed by adjusting the anodizing and annealing parameters.This is provided to investigate different phenomena by selectively adjusting a specific parameter of the Li^(+)insertion mechanism.In this paper,we reviewed how the morphology and crystallography of TiO_(2)nano tubes influence the electrochemical performance of Li^(+)batteries.In particular,electrochemical performances of amorphous and anatase titanium dioxide nanotube anodes were compared in detail.As we all know,TiO_(2)nanotube anodes have the advantages of nontoxicity,good stability,high safety and large specific surface area,in lithium-ion batteries.However,they suffer from poor electronic conductivity,inferior ion diffusivity and low theoretical capacity(335 mAh·g^(-1)),which limit their practical application.Generally,there are two ways to overcome the shortcomings of titanium dioxide nanotube anodes,including doping and synthesis composites.The achievements and existing problems associated with doped TiO_(2)nanotube anodes and composite material anodes are summarized in the present review.Based on the analysis of lithium insertion mechanism of titanium dioxide nanotube electrodes,the prospects and possible research directions of TiO_(2)anodes in lithiumion batteries are discussed.展开更多
TiO_(2)-based materials have been considered as one of most promising alternatives for high-performance Li(Na)-ion batteries because of the low cost,simple composition,easy synthesis,good environmental protection,exce...TiO_(2)-based materials have been considered as one of most promising alternatives for high-performance Li(Na)-ion batteries because of the low cost,simple composition,easy synthesis,good environmental protection,excellent safety and relatively high specific capacity.Nonetheless,the inferior electronic conductivity and poor ion diffusion coefficients are the biggest bottlenecks that restrict the popular application.Much effort has been focused on resolving these problems toward large-scale applications,and numerous significant advances have been accomplished.In the present work,a comprehensive overview of structure characteristics,electrochemical reaction mechanism and modification strategies of TiO_(2)-based materials was presented.The recent advances of various efficient ways for improving conductivity,Li(Na)storage capacity,rate capability and cycle stability are systematically summarized,including surface engineering,constructing composite and element doping,etc.Constructing TiO_(2)-based materials with novel porous heterogeneous core-shell structures have been regarded as one of the most effective ways to resolve these challenges.Finally,the future research directions and development prospects of TiO_(2)-based anode materials used in the manufacture of high-performance Li(Na)-ion batteries are prospected.This review can provide important comprehension for the construction and optimization of highperformance of TiO_(2)-based anode materials.展开更多
基金supported by the National Natural Science Foundation of China(22179063,22479078,and 22409093)the Natural Science Foundation of Jiangsu Province of China(BK20240579)。
文摘FeS_(2)is a promising anode material for potassium-ion batteries(PIBs),with the advantages of low cost and high capacity.However,it still faces challenges of capacity fading and poor rate performance in potassium storage.Rational structural design is one way to overcome these drawbacks.In this work,MIL-88B-Fe-derived FeS_(2)nanoparticles/N-doped carbon nanofibers(M-FeS_(2)@CNFs)with expansion buffer capability are designed and synthesized for high-performance PIB anodes via electrospinning and subsequent sulfurization.The uniformly distributed cavity-type porous structure effectively mitigates the severe aggregation problem of FeS_(2)nanoparticles during cycling and buffers the volume change,further enhancing the potassium storage capacity.Meanwhile,the robust KF-rich solid electrolyte interphase induced by methyl trifluoroethylene carbonate(FEMC)additive improves the cycling stability of the M-FeS_(2)@CNF anode.In the electrolyte with 3 wt%FEMC,the M-FeS_(2)@CNF anode shows a reversible specific capacity of 592.7 mA h g^(-1)at 0.1 A g^(-1),an excellent rate capability of 327.1 mA h g^(-1)at 5 A g^(-1),and a retention rate 80.7%over 1000 cycles at 1 A g^(-1).More importantly,when assembled with a K_(1.84)Ni[Fe(CN)_(6)]_(0.88)·0.49H_(2)O cathode,the full battery manifests excellent cycle stability and high rate performance.This study demonstrates the significant importance of the synergistic effect of structural regulation and electrolyte optimization in achieving high cycling stability of PIBs.
基金supported by the Natural Science Foundation of Henan Province(222300420083)the Opening Foundation of State Key Laboratory of Chemistry and Utilization of Carbonbased Energy Resource of Xinjiang University(KFKT2021004)supported by the National Supercomputing Center in Zhengzhou and the Shanxi Supercomputing Center。
文摘The distinguishing feature of Fe_(3)GeTe_(2)lies in its robu st in-plane chemical bonds within layers,which are interconnected by the weak van der Waals forces between adjacent layers,offering a stable framework characterized by enhanced interlayer spacing,thereby facilitating the migration of large-sized alkali metal ions.However,to date,there have been no reported studies on the ion storage performance of Fe_(3)GeTe_(2).In this study,Fe_(3)GeTe_(2)is synthesized via the chemical vapor transport method to assess its sodium/potassium storage capabilities.Fe_(3)GeTe_(2)is characterized by its impressive conductivity,a distinctive layered architecture,and a notably wide interlayer spacing,all of these attributes collectively contributing to its superior ion storage proficiency in both sodium-ion batteries(SIBs)and potassiumion batteries(PIBs).Specifically,it demonstrates exceptional electrochemical performance,maintaining a capacity of 291.8 mA h g^(-1)at 5 A g^(-1)in SIBs and 125.0 mA h g^(-1)over 6000 cycles at 3 A g^(-1)in PIBs.A series of in/ex situ characterizations uncover the reaction mechanism of Fe_(3)GeTe_(2)in the both systems,involving a combined process of intercalation,conversion,and alloying.Theoretical calculations provide further insights into the high ion adsorption affinity and diffusion kinetics of Fe_(3)GeTe_(2)in these systems.Analytical findings reveal its superior electrochemical performance in SIBs compared to PIBs,owing to higher diffusion kinetics and reactivity.This research establishes both experimental evidence and theoretical underpinnings for the utilization of Fe_(3)GeTe_(2)in SIBs and PIBs,opening up a new avenue for the utilization of germanium-based ternary materials in the field of energy storage.
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supported by the National Key Research and Development Program of China(No.2022YFB2502000)the National Natural Science Foundation of China(Nos.U21A2033251771076,52301266,42203047)+2 种基金R&D Program in Key Areas of Guangdong Province(No.2020B0101030005)Science and Technology Planning Project of Guangzhou(No.2024A04J9999)GDUT Large-Scale Instruments Open Foundation(No.ATC2022201)。
文摘Transition metal selenides are considered promising electrochemical energy storage materials due to their excellent rate properties and high capacity based on multi-step conversion reactions.However,its practical applications are hampered by poor conductivity and large volume variation for Na^(+)storage,which resulting fast capacity decay.Herein,a facile metal-organic framework(MOF)derived method is explored to embed Cu_(2-x)Se@C particles into a carbon nanobelts matrix.Such carbon encapsulated nanobelts'structural moderate integral electronic conductivity and maintained the structure from collapsing during Na^(+)insertion/extraction.Furthermore,the porous structure of these nanobelts endows enough void space to mitigate volume stress and provide more diffusion channels for Na^(+)/electrons transporting.Due to the unique structure,these Cu_(2-x)Se@C nanobelts achieved ultra-stable cycling performance(170.7 m Ah/g at1.0 A/g after 1000 cycles)and superior rate capability(94.6 m Ah/g at 8 A/g)for sodium-ion batteries.The kinetic analysis reveals that these Cu_(2-x)Se@C nanobelts with considerable pesoudecapactive contribution benefit the rapid sodiation/desodiation.This rational design strategy broadens an avenue for the development of metal selenide materials for energy storage devices.
基金supported by the National Natural Science Foundation of China(22272150)the Major Program of Zhejiang Provincial Natural Science Foundation of China(LD22B030002)+2 种基金the Zhejiang Provincial Ten Thousand Talent Program(2021R51009)the Zhejiang Provincial Natural Science of China(LZ23B030001)the Key Science and Technology Project of Jinhua City(2022-1-083,2023-1-093).
文摘Aqueous zinc-ion batteries(ZIBs)are promising candidates for next-generation energy storage,but the problems related to Zn dendrites and side reactions severely hinder their practical applications.Herein,a self-recognition separator based on a Bi-based metal-organic framework(GF@CAU-17)is developed for ion management to achieve highly reversible Zn anodes.The GF@CAU-17 has self-recognition behavior to customize selective Zn^(2+)channels,effectively repelling SO_(4)^(2-)and H_(2)O,but facilitating Zn^(2+)conduction.The inherent properties of CAU-17 result in the repulsion of SO_(4)^(2-)ions while disrupting the hydrogen bond network among free H_(2)O molecules,restraining side reactions and by-products.Simultaneously,the zincophilic characteristic of CAU-17 expedites the desolvation of[Zn(H_(2)O)6]^(2+),leading to a self-expedited Zn^(2+)ion pumping effect that dynamically produces a steady and homogeneous Zn^(2+)ion flux,and thereby alleviates concentration polarization.Consequently,a symmetric cell based on the GF@CAU-17 separator can achieve a long lifespan of 4450 h.Moreover,the constructed Zn//GF@CAU-17//MnO_(2)cell delivers a high specific capacity of 221.8 mAh g^(-1)and 88.0%capacity retention after 2000 cycles.
基金National Natural Science Foundation of China(No.61376017)。
文摘SnO_(2)-based anodes for lithium-ion batteries(LIBs)experience volume expansion,leading to rapid capacity decay and low conductivity.To address this problem,a composite consists of C/SnO_(2) with a core-shell structure and a carbonized nitrogen-doped Co-metal organic framework(Co-MOF)(NC)supported on carbon cloth(CC)was designed and prepared,which was denoted as C/SnO_(2)@NC@CC.C/SnO_(2)@NC@CC could be used directly as a flexible anode for LIBs.The combination of core-shell structure centered on carbon spheres,carbonized nitrogen-doped Co-MOF,and CC not only restricts the volume expansion but also functions as conductive networks to improve the electrical conductivity.C/SnO_(2)@NC@CC exhibits excellent electrochemical performance with charge and discharge specific capacities of 2066.0 and 2077.1 mAh/g,respectively,after 120 cycles at a current density of 0.5 A/g.
文摘This work is devoted to the development of a low cost dimensionally stable anode with high oxygen evolution catalytic activity for practical applications.For this purpose,a Ti/SnO_(x)/MnO_(2) anode was fabricated through an innovative strategy involving Sn electrodeposition,oxidation,and MnO_(2)-layer preparation.The structure of the anode was characterized,and the oxygen evolution performance was evaluated in a H_(2)SO_(4) solution.The results show that compared with the Ti/SnO_(2)/MnO_(2) anode prepared by the conventional brushing-annealing process,the Ti/SnO_(x)/MnO_(2) anode fabricated through the innovative procedure exhibits a lower oxygen evolution potential and a nearly 40%longer accelerated lifespan.The superior oxygen evolution performance of the Ti/SnO_(x)/MnO_(2) anode is attributed to the distinctive SnO_(x) intermediate layer fabricated through Sn electrodeposition followed by oxidation,which indicates the great potential of the anode as a dimensionally stable anode for metal electrowinning and hydrogen production by electrolysis,etc.
基金supported by National Natural Science Foundation of China(Nos.52307239,52102300,52207234)the Natural Science Foundation of Hubei Province(Nos.2022CFB1003,2021CFA025).
文摘Conversion-type anode materials are highly desirable for Na-ion batteries(NIBs)due to their high theoretical capacity.Nevertheless,the active materials undergo severe expansion and pulverization during the sodiation,resulting in inferior cycling stability.Herein,a self-supporting three-dimensional(3D)graphene sponge decorated with Fe_(2)O_(3)nanocubes(rGO@Fe_(2)O_(3))is constructed.Specifically,the 3D graphene sponge with resilience and high porosity benefits to accommodate the volume expansion of the Fe_(2)O_(3)nanocubes and facilitates the rapid electrons/ions transport,enabling spatial confinement to achieve outstanding results.Besides,the free-standing rGO@Fe_(2)O_(3)can be directly used as an electrode without additional binders and conductive additives,which helps to obtain a higher energy density.Based on the total mass of the rGO@Fe_(2)O_(3)material,the rGO@Fe_(2)O_(3)anode presents a specific capacity of 859 mAh/g at 0.1 A/g.It also delivers an impressive cycling performance(327 mAh/g after 2000 cycles at 1 A/g)and a superior rate capacity(162mAh/g at 20 A/g).The coin-type Na_(3)V_(2)(PO_(4))_(3)@C//rGO@Fe_(2)O_(3)NIB exhibits an energy density of 265.3Wh/kg.This unique 3D ionic/electronic conductive network may provide new strategies to design advanced conversion-type anode materials for high-performance NIBs.
基金financially supported by the National Natural Science Foundation of China(No.22301151)the Natural Science Foundation of Inner Mongolia Autonomous Region of China(No.2022QN05024)+1 种基金the Science and Technology Projects of Inner Mongolia Autonomous Region(No.2024SKYPT0011)the Science and Technology Planning Project of Hohhot,China(No.2024-JieBangGuaShuai-Gao-4)
文摘In sulfide-based all-solid-state lithium batteries(ASLBs),the development of high-capacity anode materials with stable interfaces to sulfide solid-state electrolytes(SSEs)is critical.Here,In_(2)O_(3)is explored as an anode material for ASLBs for the first time,demonstrating exceptional interfacial stability and electrochemical performance.The In_(2)O_(3)anode,with a substantial mass loading of 7.64 mg cm^(-2),sustains a charge-specific capacity of528.0 mAh g^(-1)(4.03 mAh cm^(-2))at a current density of0.76 mA cm^(-2)over 500 cycles,with a capacity retention of 81.2%.Additionally,it exhibits remarkable long-term cycling stability(2900 cycles)under a high current density of 3.82 mA cm^(-2),with an exceptionally low decay rate of0.016%per cycle.The charge-discharge mechanism of the In_(2)O_(3)anode is elucidated in detail,revealing that the electrochemical evolution of In_(2)O_(3)in ASLBs involves notonly the alloying/dealloying process of indium(In)but also a conversion reaction between In and Li_(2)O.Notably,as cycling progresses,the conversion reaction of In and Li_(2)O diminishes,with the reversible alloy ing/dealloy ing process becoming predominant.This work offers valuable insights for advancing oxide anode materials in sulfide-based ASLBs.
基金National Natural Science Foundation of China (52301273, 52072411)Science and Technology Innovation Program of Hunan Province (2024RC3222)+3 种基金Key project of scientific research project of Hunan Provincial Department of Education (22A0479)China Postdoctoral Science Foundation (2024M753668)Central South University Innovation-Driven Research Programme (2023CXQD038)Hunan Provincial Postgraduate Research Innovation Programme(CX20240970)。
文摘Aqueous zinc-ion batteries (AZIBs) are fundamentally challenged by the instability of the electrode/electrolyte interface,predominantly due to irreversible zinc (Zn) deposition and hydrogen evolution.Particularly,the intricate mechanisms behind the electrochemical discrepancies induced by interfacial Zn^(2+)-solvation and deposition behavior demand comprehensive investigation.Organic molecules endowed with special functional groups (such as hydroxyl,carboxyl,etc.) have the potential to significantly optimize the solvation structure of Zn^(2+)and regulate the interfacial electric double layer (EDL).By increasing nucleation overpotential and decreasing interfacial free energy,these functional groups facilitate a lower critical nucleation radius,thereby forming an asymptotic nucleation model to promote uniform Zn deposition.Herein,this study presents a pioneering approach by introducing trace amounts of n-butanol as solvation regulators to engineer the homogenized Zn (H-Zn) anode with a uniform and dense structure.The interfacial reaction and structure evolution are explored by in/ex-situ experimental techniques,indicating that the H-Zn anode exhibits dendrite-free growth,no by-products,and weak hydrogen evolution,in sharp contrast to the bare Zn.Consequently,the H-Zn anode achieves a remarkable Zn utilization rate of approximately 20% and simultaneously sustains a prolonged cycle life exceeding 500 h.Moreover,the H-Zn//NH_(4)V_(4)O^(10)(NVO) full battery showcases exceptional cycle stability,retaining 95.04%capacity retention after 400 cycles at a large current density of 5 A g^(-1).This study enlightens solvation-regulated additives to develop Zn anode with superior utilization efficiency and extended operational lifespan.
基金Project(2017YFB0305401)supported by the National Key R&D Program of ChinaProjects(51874369,51474245,51871249)supported by the National Natural Science Foundation of China+1 种基金Project(2018JJ3659)supported by the Natural Science Foundation of Hunan Province,ChinaProject(2018RS3007)supported by Huxiang Young Talents Plan,China
文摘Pb?Ag?PbO2 composite anodes with different mass fractions(1%,2%,3%,4%and 5%)ofβ-PbO2 were prepared by powder-pressed(PP)method.The galvanostatic polarization curves,Tafel curves and anodic polarization curves were tested in sulfuric acid solution.The morphologies and phase compositions of the anodic layers formed after galvanostatic polarization were investigated by using scanning electron microscope(SEM)and X-ray diffractometer(XRD),respectively.The results showed thatβ-PbO2 can improve the electrocatalytic activity of anodic oxide.The anode containing 3%β-PbO2 had the lowest overpotential of oxygen evolution reaction(OER)and the best corrosion resistance.The morphologies of the anode surfaces were gradually transformed from regular crystals to amorphous ones as the content ofβ-PbO2 increased in anodes.
基金Project(51474238)supported by the National Natural Science Foundation of China
文摘A comparative study on the corrosion resistance of 17Ni/（NiFe2O4-10NiO） cermet inert anode prepared in differentsintering atmospheres was conducted in Na3AlF6-Al2O3 melt. The results indicate that the corrosion rates of NiFe2O4-based cermetanodes prepared in the vacuum and the atmosphere with oxygen content of 2×10^-3 （volume fraction） are 6.46 and 2.71 cm/a,respectively. Though there is a transition layer with lots of holes or pores, a densified layer is formed on the surface of anode due tosome reactions producing aluminates. For the anode prepared in the atmosphere with oxygen content of 2×10^-3, the thickness of thedensification layer （about 50 μm） is thicker than that （about 30 μm） formed on the surface of anode prepared in the vacuum. Thecontents of NiO and Fe（II） in NiFe2xO4-y-z increase with the decrease of oxygen content in sintering atmosphere, which reduces thecorrosion resistance of the material.
基金Project (2012FJ6123) supported by the Project of Science and Technology of Hunan Province,ChinaProject supported by Post-Doctoral Foundation of Central South University,China+1 种基金Project (CL12100) supported the Undergraduate Innovative Training of Central South University,ChinaProject (2282013bkso13) supported by Free Exploration Plan of Central South University,China
文摘NiFe2O4-10NiO-based cermet inert anodes for aluminium electrolysis were prepared and their properties were investigated in a lab-scale electrolysis cell. The results show that the inert anodes exhibit good performance during electrolysis in molten salt cryolite at 960 °C, but according to the analyses of phase compositions and microstructures through XRD, SEM/EDX and metallographic analysis, the metal in the anodes is preferentially corroded and many pores are produced on the anode surface after electrolysis. The preferential dissolution of Fe in the NiFe2O4 phase may lead to the non-uniform corrosion of NiFe2O4 grains. Moreover, a dense protective layer of NiFe2O4-NiAl2O4-FeAl2O4 is formed on the anode surface, which originates from the reaction of Al2O3 dissolved in the electrolyte with NiO or FeO, the annexation of NiFe2O4-NiAl2O4-FeAl2O4 to NiO and volume expansion. Thus, the dense NiFe2O4-NiAl2O4-FeAl2O4 layer inhibits the metal loss and ceramic-phase corrosion on the surface of the cermet inert anodes.
基金Project(51404001)supported by the National Natural Science Foundation of ChinaProject([2014]1685)supported by the Scientific Research Foundation for the Returned Overseas Chinese Scholars,Ministry of Education,China
文摘A novel SnO2-based gas anode was developed for aluminum electrolysis in molten cryolite at 850 ＆#176;C to reduce energy consumption and decrease CO2 emissions. Hydrogen was introduced into the anode, participating in the anode reaction. Carbon and aluminum were used as the cathode and reference electrodes, respectively. Cyclic voltammetry was applied in the cell to investigate the electrochemical behavior of oxygen ion on platinum and SnO2-based materials. The potential for oxygen evolution on these electrode materials was determined. Then, galvanostatic electrolysis was performed on the gas anode, showing a significant depolarization effect （a decrease of ~0.8 V of the anode potential） after the introduction of hydrogen, compared with no gas introduction or the introduction of argon. The results indicate the involvement of hydrogen in the anode reaction （three-phase-boundary reaction including gas, electrolyte and electrode） and give the possibility for the utilization of reducing gas anodes for aluminum electrolysis.
基金supported by the National Natural Science Foundation of China (Grant No. 51302079)the National Natural Science Foundation of Hunan Province (Grant No. 2017JJ1008)
文摘It is urgent to solve the problems of the dramatic volume expansion and pulverization of SnO_2 anodes during cycling process in battery systems. To address this issue, we design a hybrid structure of N-doped carbon fibers@SnO_2 nanoflowers(NC@SnO_2) to overcome it in this work. The hybrid NC@SnO_2 is synthesized through the hydrothermal growth of SnO_2 nanoflowers on the surface of N-doped carbon fibers obtained by electrospinning. The NC is introduced not only to provide a support framework in guiding the growth of the SnO_2 nanoflowers and prevent the flower-like structures from agglomeration, but also serve as a conductive network to accelerate electronic transmission along one-dimensional structure effectively. When the hybrid NC@SnO_2 was served as anode, it exhibits a high discharge capacity of 750 Ah g^(-1) at 1 A g^(-1) after 100 cycles in Li-ion battery and 270 mAh g^(-1) at 100 mA g^(-1) for 100 cycles in Na-ion battery, respectively.
基金the National Natural Science Foundation of China (Grant No. 21701144)the China Postdoctoral Science Foundation (Grant Nos. 2016M592303 and 2017T100536)
文摘Constructing unique and highly stable structures with plenty of electroactive sites in sodium storage materials is a key factor for achieving improved electrochemical properties through favorable sodium ion di usion kinetics. An SnS_2@carbon hollow nanospheres(SnS_2@C) has been designed and fabricated via a facile solvothermal route, followed by an annealing treatment. The SnS_2@C hybrid possesses an ideal hollow structure, rich active sites, a large electrode/electrolyte interface, a shortened ion transport pathway, and, importantly, a bu er space for volume change, generated from the repeated insertion/extraction of sodium ions. These merits lead to the significant reinforcement of structural integrity during electrochemical reactions and the improvement in sodium storage properties, with a high specific reversible capacity of 626.8 mAh g^(-1) after 200 cycles at a current density of 0.2 A g^(-1) and superior high-rate performance(304.4 mAh g^(-1) at 5 A g^(-1)).
基金financially supported by the National Natural Science Foundation of China(Nos.51704124,51762017 and 11602094)the Key Planned Science and Technology Project of Xiangxi Tujia&Miao Autonomous Prefecture(No.2018GX2001)+2 种基金the Program of Youth Talent Support for Hunan Province(No.2018RS3098)the Key Program of Hunan Provincial Education Department(No.18A285)the Natural Science Foundation of Hunan Province(Nos.2018JJ3415 and 2019JJ50485)。
文摘Sodium-ion batteries(SIBs)have attracted significant attention with respect to renewable energy power generation systems because of the abundant reserves of sodium on earth.However,anode materials are presently limited by low energy density,poor rate performance and inferior cycling stability.In recent years,tin disulfide(SnS_(2))with a particular layered structure has been considered as a promising anode material for SIBs due to its high theoretical capacity and low cost.Herein,a nervoussystem-like structured SnS_(2)/CNTs composite was successfully synthesized via a hydrothermal method.The SnS_(2)sheets were strung with carbon nanotubes(CNTs)to form a hierarchical porous structure,which is effective for electrolyte diffusion and electronic transmission.The large distance of the(001)plane(0.5899 nm)of SnS_(2)favors Na+insertion-extraction dynamics.Benefitting from these structural characteristics,SnS_(2)/CNTs electrodes exhibit high specific capacity,excellent rate performance and superior cycling stability.A high charge capacity of 642 mAh·g^(-1)was released at 0.2 A·g^(-1),and then,a high reversible capacity of 427 mAh·g^(-1)was retained after 100 cycles.Even charged at 2 A·g^(-1),the SnS_(2)/CNTS electrode maintained a capacity of 282 mAh·g^(-1).The nervous-system-like structure of the SnS_(2)/CNTs composite provides a novel strategy for the development of SIBs with high electrochemical performance.
基金the National Natural Science Foundation of China(No.61376017)the Fundamental Research Funds for the Central Universities and Graduate Student Innovation Fund of Donghua University(No.CUSFDH-D-2020094)the Shanghai Sailing Program(No.17YF1400600)。
文摘Self-organized titanium dioxide(TiO_(2))nanotubes,which are prepared by electrochemical anodizing,have been widely researched as promising anodes for Liion batteries.Both nanotubular morphology and bulk structure of TiO_(2)nanotubes can be easily changed by adjusting the anodizing and annealing parameters.This is provided to investigate different phenomena by selectively adjusting a specific parameter of the Li^(+)insertion mechanism.In this paper,we reviewed how the morphology and crystallography of TiO_(2)nano tubes influence the electrochemical performance of Li^(+)batteries.In particular,electrochemical performances of amorphous and anatase titanium dioxide nanotube anodes were compared in detail.As we all know,TiO_(2)nanotube anodes have the advantages of nontoxicity,good stability,high safety and large specific surface area,in lithium-ion batteries.However,they suffer from poor electronic conductivity,inferior ion diffusivity and low theoretical capacity(335 mAh·g^(-1)),which limit their practical application.Generally,there are two ways to overcome the shortcomings of titanium dioxide nanotube anodes,including doping and synthesis composites.The achievements and existing problems associated with doped TiO_(2)nanotube anodes and composite material anodes are summarized in the present review.Based on the analysis of lithium insertion mechanism of titanium dioxide nanotube electrodes,the prospects and possible research directions of TiO_(2)anodes in lithiumion batteries are discussed.
基金financially supported by the National Natural Science Foundation of China(No.51774002)the Key Program for International S&T Cooperation Projects of China(No.2017YFE0124300)the“333 Talent Project”of Hebei Province(No.A202005018)。
文摘TiO_(2)-based materials have been considered as one of most promising alternatives for high-performance Li(Na)-ion batteries because of the low cost,simple composition,easy synthesis,good environmental protection,excellent safety and relatively high specific capacity.Nonetheless,the inferior electronic conductivity and poor ion diffusion coefficients are the biggest bottlenecks that restrict the popular application.Much effort has been focused on resolving these problems toward large-scale applications,and numerous significant advances have been accomplished.In the present work,a comprehensive overview of structure characteristics,electrochemical reaction mechanism and modification strategies of TiO_(2)-based materials was presented.The recent advances of various efficient ways for improving conductivity,Li(Na)storage capacity,rate capability and cycle stability are systematically summarized,including surface engineering,constructing composite and element doping,etc.Constructing TiO_(2)-based materials with novel porous heterogeneous core-shell structures have been regarded as one of the most effective ways to resolve these challenges.Finally,the future research directions and development prospects of TiO_(2)-based anode materials used in the manufacture of high-performance Li(Na)-ion batteries are prospected.This review can provide important comprehension for the construction and optimization of highperformance of TiO_(2)-based anode materials.
