Progress,challenges,and prospects of spent lithium-ion batteries recycling:A review

The recycling and reutilization of spent lithium-ion batteries(LIBs)have become an important measure to alleviate problems like resource scarcity and environmental pollution.Although some progress has been made,battery recycling technology still faces challenges in terms of efficiency,effectiveness and environmental sustainability.This review aims to systematically review and analyze the current status of spent LIB recycling,and conduct a detailed comparison and evaluation of different recycling processes.In addition,this review introduces emerging recycling techniques,including deep eutectic solvents,molten salt roasting,and direct regeneration,with the intent of enhancing recycling efficiency and diminishing environmental repercussions.Furthermore,to increase the added value of recycled materials,this review proposes the concept of upgrading recycled materials into high value-added functional materials,such as catalysts,adsorbents,and graphene.Through life cycle assessment,the paper also explores the economic and environmental impacts of current battery recycling and highlights the importance that future recycling technologies should achieve a balance between recycling efficiency,economics and environmental benefits.Finally,this review outlines the opportunities and challenges of recycling key materials for next-generation batteries,and proposes relevant policy recommendations to promote the green and sustainable development of batteries,circular economy,and ecological civilization.

Tuning interface mechanism of FeCo alloy embedded N,S-codoped carbon substrate for rechargeable Zn-air battery

The interface mechanism between catalyst and carbon substrate has been the focus of research.In this paper,the FeCo alloy embedded N,S co-doped carbon substrate bifunctional catalyst(FeCo/S-NC)is obtained by a simple one-step pyrolysis strategy.The experimental results and density functional theory(DFT)calculation show that the formation of FeCo alloy is conducive to promoting electron transfer,and the introduction of S atom can enhance the interaction between FeCo alloy and carbon substrate,thus inhibiting the migration and agglomeration of particles on the surface of carbon material.The FeCo/SNC catalysts show outstanding performance for oxygen reduction reaction(ORR)and oxygen evolution reaction(OER).FeCo/S-NC shows a high half-wave potential(E_(1/2)=0.8823 V)for ORR and a low overpotential at 10 mA cm^(-2)(E_(j=10)=299 mV)for OER.In addition,compared with Pt/C+RuO_(2) assembled Zn-air battery(ZAB),the FeCo/S-NC assembled ZAB exhibits a larger power density(198.8 mW cm^(-2)),a higher specific capacity(786.1 mA h g_(zn)~(-1)),and ultra-stable cycle performance.These results confirm that the optimized composition and the interfacial interaction between catalyst and carbon substrate synergistically enhance the electrochemical performance.

The mystic role of high-entropy designs in rechargeable metal-ion batteries:A review

Rechargeable metal-ion batteries, such as lithium-ion batteries(LIBs) and sodium-ion batteries(SIBs),have raised more attention because of the large demand for energy storage solutions. Undoubtedly, electrode materials and electrolytes are key parts of batteries, exhibiting critical influence on the reversible capacity and span life of the metal-ion battery. Nonetheless, researchers commonly express concerns regarding the stability of both electrodes and electrolytes. Given its commendable stability attributes,high-entropy materials have garnered widespread acclaim and have been applied in many fields since their inception, notably in energy storage. However, while certain high-entropy designs have achieved substantial breakthroughs, some have failed to meet anticipated outcomes within the high energy density energy storage materials. Moreover, there is a lack of comprehensive summary research on the corresponding mechanisms and design principles of high-entropy designs. This review examines the current high-entropy designs for cathodes, anodes, and electrolytes, aiming to summarize the design principle,potential mechanisms, and electrochemical performance. We focus on their structural characteristics,interface characteristics, and prospective development trends. At last, we provide a fair evaluation along-side succinct development suggestions.

Modification,application and expansion of electrode materials based on cobalt telluride

Metal(Li,Na,K,Al)-ion batteries and lithium-sulfur and lithium-tellurium batteries are gaining recognition for their eco-friendly characteristics,substantial energy density,and sustainable attributes.However,the overall performance of rechargeable batteries heavily depends on their electrode materials.Transition metal tellurides have recently gained significant attention due to their high electrical conductivity and density.Cobalt telluride has received the most extensive research due to its catalytic activity,unique magnetic properties,and diverse composition and crystal structure.Nevertheless,its limited conductivity and significant volume variation contribute to electrode structural deterioration and rapid capacity decline.This review comprehensively summarizes recent advances in rational design and synthesis of modified cobalt telluride-based electrodes,encompassing defect engineering(Te vacancies,cation vacancies,heterointerfaces,and homogeneous interfaces)and composite engineering(derived carbon from precursors,carbon fibers,Mxene,graphene nanosheets,etc.).Particularly,the intricate evolution mechanisms of the conversion reaction process during cycling are elucidated.Furthermore,these modified strategies applied to other transitional metal tellurides,such as iron telluride,nickel telluride,zinc telluride,copper telluride,molybdenum telluride,etc.,are also thoroughly summarized.Additionally,their application extends to emerging aqueous zinc-ion batteries.Finally,potential challenges and prospects are discussed to further propel the development of transition metal tellurides electrode materials for next-generation rechargeable batteries.

Rational construction and decoration of Li_(5)Cr_(7)Ti_(6)O_(25)@Cnanofibers as stable lithium storage materials

Li_(5)Cr_(7)Ti_(6)O_(25) is regarded as a promising anode material for Li-ion batteries(LIBs)because of its low cost and high theoretical capacity.However,the inherently poor conductivity significantly limits the enhancement of its rate capability and cycling stability,especially at high current densities.In this work,we construct one-dimensional Li_(5)Cr_(7)Ti_(6)O_(25)/C nanofibers by electrospinning method to enhance the kinetic,which realizes high cycling stability.Carbon coating enhances the structure stability,insertion/extraction reversibility of Li-ions and electrochemical reaction activity,and facilitates the transfer of Li-ions.Benefited from the unique architecture and component,the Li_(5)Cr_(7)Ti_(6)O_(25)/C(6.6 wt%)nanofiber shows an excellent rate capability with a reversible de-lithiation capacity of 370.8,290.6,269.2,254.3 and 244.9 m Ah g^(-1) at 200,300,500,800 and 1000 m A g^(-1),respectively.Even at a higher current density of 1 A g^(-1),Li_(5)Cr_(7)Ti_(6)O_(25)/C(6.6 wt%)nanofiber shows high cycling stability with an initial de-lithiation capacity of 237.8 m Ah g^(-1) and a capacity retention rate of about 84%after 500 cycles.The density functional theory calculation result confirms that the introduction of carbon on the surface of Li_(5)Cr_(7)Ti_(6)O_(25) changes the total density of states of Li_(5)Cr_(7)Ti_(6)O_(25),and thus improves electronic conductivity of the composite,resulting in a good electrochemical performance of Li_(5)Cr_(7)Ti_(6)O_(25)/C nanofibers.Li_(5)Cr_(7)Ti_(6)O_(25)/C nanofibers indicate a great potential as an anode material for the next generation of high-performance LIBs.

Regulating the electrochemical activity of Fe-Mn-Cu-based layer oxides as cathode materials for high-performance Na-ion battery

Fe-Mn based layer oxides cathode materials have attracted widespread attention as a potential candidate for sodium-ion batteries(SIBs)owing to the earth abundance,cost-effectiveness and acceptable specific capacity.However,the irreversible phase transition often brings rapid capacity decay,which seriously hinders the practical application in large-scale energy storage.Herein,we design a nickel-doped Na_(0.70)Fe_(0.10)Cu_(0.20)Ni_(0.05)Mn_(0.65)O_(2)(NFCNM-0.05)cathode material of SIBs with activated anionic redox reaction,and then inhibit the harmful phase transition.The ex-situ X-ray diffraction patterns demonstrate the NFCNM-0.05 always keeps the P2 phase during the sodiation/desodiation process,indicating a high structure stability.The ex-situ X-ray photoelectron spectroscopy implies the redox reactions between O2-and O-occur in the charging process,which offers extra specific capacity.Thus,the NFCNM-0.05 electrode delivers a high initial discharge capacity of 148 mA h g-1and remains a prominent cycling stability with an excellent capacity retention of 95.9%after 200 cycles at 1 C.In addition,the electrochemical impedance spectroscopy and galvanostatic intermittent titration technique show the NFCNM-0.05 electrode possesses fast ion diffusion ability,which is beneficial for the enhancement of rate performance.Even at 10 C,the NFCNM-0.05 can offer a reversible discharge capacity of 81 mA h g-1.DFT calculation demonstrates the doping of appropriate amount of Ni ions is benefit for the enhancement of the electrochemical performance of the layer oxides.This work provides an effective strategy to enhance the electrochemical performance of Fe-Mn based cathode materials of SIBs.

Understanding of the charge storage mechanism of MnO_(2)-based aqueous zinc-ion batteries:Reaction processes and regulation strategies

Though secondary aqueous Zn ion batteries(AZIBs)have been received broad concern in recent years,the development of suitable cathode materials of AZIBs is still a big challenge.The MnO_(2) has been deemed as one of most hopeful cathode materials of AZIBs on account of some extraordinary merits,such as richly natural resources,low toxicity,high discharge potential,and large theoretical capacity.However,the crystal structure diversity of MnO_(2) results in an obvious various of charge storage mechanisms,which can cause great differences in electrochemical performance.Furthermore,several challenges,including intrinsic poor conductivity,dissolution of manganese and sluggish ion transport dynamics should be conquered before real practice.This work focuses on the reaction mechanisms and recent progress of MnO_(2)-based materials of AZIBs.In this review,a detailed review of the reaction mechanisms and optimal ways for enhancing electrochemical performance for MnO_(2)-based materials is proposed.At last,a number of viewpoints on challenges,future development direction,and foreground of MnO_(2)-based materials of aqueous zinc ions batteries are put forward.This review clarifies reaction mechanism of MnO_(2)-based materials of AZIBs,and offers a new perspective for the future invention in MnO_(2)-based cathode materials,thus accelerate the extensive development and commercialization practice of aqueous zinc ions batteries.

Advancement of technology towards high-performance non-aqueous aluminum-ion batteries

Al-ion batteries(AIBs) have been identified as one of the most hopeful energy storage systems after Li-ion batteries on account for the ultrahigh volumetric capacity,high safety and low cost from the rich abundance of Al.Nonetheless,some inevitable shortcomings,such as the formation of passive oxide film,hydrogen side reactions and anode corrosion,finally limit the large-scale application of aqueous AIBs.The nonaqueous AIBs have been considered as one of most hopeful alternatives for high-powered electrochemical energy storage devices.Nonetheless,various technical and scientific obstacles should be resolved because nonaqueous AIBs are still nascent.Some significant efforts have aimed to resolve these issues towards large-scale applications,and some important advancement has been made.In the present review,we mainly intended to offer an overview of non-aqueous AIBs systems,and we comprehensively reviewed the recent research advancement of the cathode materials,anode materials electrolyte and collectors as well as the fundamental understanding of the functional mechanisms.In addition,we have also analyzed several technical challenges and summarized the strategies used for overcoming the challenges in improving the electrochemical properties,including morphology control,surface engineering,doping and construction of composite electrodes as well as the charge storage mechanisms of the materials with different crystal structures.At last,future research orientation and development prospect of the AIBs are proposed.

First-principles calculations of Ni–(Co)–Mn–Cu–Ti all-d-metal Heusler alloy on martensitic transformation,mechanical and magnetic properties

The martensitic transformation,mechanical,and magnetic properties of the Ni_(2)Mn_(1.5-x)Cu_(x)Ti_(0.5) (x=0.125,0.25,0.375,0.5) and Ni_(2-y)Co_(y)Mn_(1.5-x)Cu_(x)Ti_(0.5)[(x=0.125,y=0.125,0.25,0.375,0.5) and (x=0.125,0.25,0.375,y=0.625)]alloys were systematically studied by the first-principles calculations.For the formation energy,the martensite is smaller than the austenite,the Ni–(Co)–Mn–Cu–Ti alloys studied in this work can undergo martensitic transformation.The austenite and non-modulated (NM) martensite always present antiferromagnetic state in the Ni_(2)Mn_(1.5-x)Cu_(x)Ti_(0.5) and Ni_(2-y)Co_(y)Mn_(1.5-x)Cu_(x)Ti_(0.5) (y<0.625) alloys.When y=0.625 in the Ni_(2-y)Co_(y)Mn_(1.5-x)Cu_(x)Ti_(0.5) series,the austenite presents ferromagnetic state while the NM martensite shows antiferromagnetic state.Cu doping can decrease the thermal hysteresis and anisotropy of the Ni–(Co)–Mn–Ti alloy.Increasing Mn and decreasing Ti content can improve the shear resistance and normal stress resistance,but reduce the toughness in the Ni–Mn–Cu–Ti alloy.And the ductility of the Co–Cu co-doping alloy is inferior to that of the Ni–Mn–Cu–Ti and Ni–Co–Mn–Ti alloys.The electronic density of states was studied to reveal the essence of the mechanical and magnetic properties.

Defect Engineering of Disordered Carbon Anodes with Ultra-High Heteroatom Doping Through a Supermolecule-Mediated Strategy for Potassium-Ion Hybrid Capacitors

Amorphous carbons are promising anodes for high-rate potassium-ion batteries.Most low-temperature annealed amorphous carbons display unsatisfactory capacities.Heteroatom-induced defect engineering of amorphous carbons could enhance their reversible capacities.Nevertheless,most lignocellulose biomasses lack heteroatoms,making it a challenge to design highly heteroatom-doped carbons(>10 at%).Herein,we report a new preparation strategy for amorphous carbon anodes.Nitrogen/sulfur co-doped lignin-derived porous carbons(NSLPC)with ultra-high nitrogen doping levels(21.6 at%of N and 0.8 at%of S)from renewable lignin biomacromolecule precursors were prepared through a supramolecule-mediated pyrolysis strategy.This supermolecule/lignin composite decomposes forming a covalently bonded graphitic carbon/amorphous carbon intermediate product,which induces the formation of high heteroatom doping in the obtained NSLPC.This unique pyrolysis chemistry and high heteroatom doping of NSLPC enable abundant defective active sites for the adsorption of K+and improved kinetics.The NSLPC anode delivered a high reversible capacity of 419 mAh g^(-1)and superior cycling stability(capacity retention of 96.6%at 1 A g^(-1)for 1000 cycles).Potassiumion hybrid capacitors assembled by NSLPC anode exhibited excellent cycling stability(91%capacity retention for 2000 cycles)and a high energy density of 71 Wh kg^(-1)at a power density of 92 W kg^(-1).

Towards high-performance anodes:Design and construction of cobalt-based sulfide materials for sodium-ion batteries

Sodium-ion batteries are increasingly becoming important in the energy storage field owing to their low cost and high natural abundance of sodium.Cobalt-based sulfide materials have been extensively studied as anode materials owing to their remarkable Na storage capability.Nevertheless,the application of cobalt-based sulfides is hampered by their serious capacity degradation and unsatisfactory cycling stability due to severe structural changes during cycling.Therefore,it is important to comprehensively summarize advances in the understanding and modification of cobalt-based sulfides from various perspectives.In the present review,recent advances on various cobalt-based sulfides,such as CoS,CoS_(2),Co_(3)S_(4),Co_(9)S_(8),NiCo_(2)S_(4),CUCo_(2)S_(4),and SnCoS_(4),are outlined with particular attention paid to strategies that improve their sodium storage performance.First,the mechanisms of charge storage are introduced.Subsequently,the key barriers to their extensive application and corresponding strategies for designing high-performance cobalt-based sulfide anode materials are discussed.Finally,key developments are summarized and future research directions are proposed based on recent advancements,aiming to offer possible fascinating strategies for the future promotion of cobalt-based sulfides as anode materials applied in sodium-ion batteries.

Construction of metal-organic framework-derived Al-doped Na_(3)V_(2)(PO_(4))_(3)cathode materials for high-performance recharge-able Na-ion batteries

Na_(3)V_(2)(PO_(4))_(3)(NVP)has emerged as one of the most promising cathode materials for sodium-ion batteries(SIBs)owing to its high ionic conductivity and high theoretical energy density.However,the inherent inferior conductivity of NVP prevents its achievement of the theoretical energy density even at low rates,thereby limiting the practical application of NVP in massive energy storage.Here,Al^(3+)-doped Na_(3)V_(2−x)Al_(x)(PO_(4))_(3)(NVAP)materials derived from aluminum terephthalate(MIL-53(Al))were synthesized for the first time,and the effects of Al3+doping on the structural and electrochemical performances of NVP were investigated.The NVAP mate-rials,particularly Na_(3)V_(1.97)Al_(0.03)(PO_(4))_(3)(NVAP2),exhibited superior cycling performance and rate capabilities compared with the NVP material.NVAP2 exhibited a good rate capability,with high reversible discharge capacities of 111.6,110.3,108.9,106.6,103.4,96.9,and 88.7 mAh g^(−1)at 0.1,0.2,0.5,1,2,5,and 10C rates,respectively.Moreover,the NVAP2 material exhibited a prominent initial discharge capacity of 102.3 mAh g^(−1)and maintained an excellent capacity retention rate of 92.0%after 2000 cycles at 10C,indicating significant cycling stability.Overall,this work provides an efficient technique for enhancing the electrochemical proper-ties of cathode materials with a sodium superionic conductor structure for SIBs.

Enhanced Cycling Stability of LiCoO2 at 4.6 V by Multi-component Doping

Fig.1 3D X-ray tomography reconstruction and element distribution in Ti,Mg and Al co-doped LiCoO2.3D spatial distributions of (a) Al,(b) Co and (c) Ti probed by fluorescence-yield scanning transmission X-ray microscopy;elemental distributions of (d) Al,(e) Co and (f) Ti over the virtual x-z slice through the center of the particle;(g) identified and visualized subdomain formation Fig.2 (a) Comparison of cycling stabilities of Ti,Mg and Al co-doped LiCoO2 and pristine LiCoO2 half cells,charge-discharge profiles of (b) pristine LiCoO2 and (c) Ti,Mg and Al co-doped LiCoO2 half cells,(d) cycle stabilities of Ti,Mg and Al co-doped LiCoO2 and pristine LiCoO2 full batteries (graphite was used anode) and (e) discharge voltage of the full batteries and energy density of the both materials as a function of cycle number Layered lithium cobalt oxide (LiCoO2) with a theoretical capacity of 274 mAh·g^-1 has become a dominant cathode material for lithium-ion batteries of “3C” market (cellular phones,portable computers,camcorders)[1-2].Nevertheless,the actually attained capacity is merely about 140 mAh·g^-1 with a charge cut-off vol- tage of about 4.2 V (vs Li +/Li)[3].

Boron-doped high-entropy oxide toward high-rate and long-cycle layered cathodes for wide-temperature sodium-ion batteries

03-type layered metal oxides hold great promise for sodium-ion batteries cathodes owing to their energy density advantage.However,the severe irreversible phase transition and sluggish Na^(+)diffusion kinetics pose significant challenges to achieve high-performance layered cathodes.Herein,a boron-doped03-type high entropy oxide Na(Fe_(0.2)Co_(0.15)Cu_(0.05)Ni_(0.2)Mn_(0.2)Ti_(0.2))B_(0.02)O_(2)(NFCCNMT-B_(0.02))is designed and the covalent B-O bonds with high entropy configuration ensure a robust layered structure.The obtained cathode NFCCNMT-B_(0.02)exhibits impressive cycling performance(capacity retention of 95%and 82%after100 cycles and 300 cycles at 1 and 10 C,respectively)and outstanding rate capability(capacity of 83 mAh g^(-1)at 10 C).Furthermore,the NFCCNMT-B_(0.02)demonstrates a superior wide-temperature performance,maintaining the same capacity level(113,4 mAh g^(-1)@-20℃,121 mAh g^(-1)@25℃,and 119 mAh g^(-1)@60℃)and superior cycle stability(90%capacity retention after 100 cycles at 1 C at-20℃).The high-entropy configuration design with boron doping strategy contributes to the excellent sodium-ion storage performance.The high-entropy configuration design effectively suppresses irreversible phase transitions accompanied by small volume changes(ΔV=0.65 A3).B ions doping expands the Na layer distance and enlarges the P3 phase region,thereby enhancing Na^(+)diffusion kinetics.This work offers valuable insights into design of high-performance layered cathodes for sodium-ion batteries operating across a wide temperature.

Boosting overall saline water splitting by constructing a strain-engineered high-entropy electrocatalyst

High-entropy materials(HEMs),which are newly manufactured compounds that contain five or more metal cations,can be a platform with desired properties,including improved electrocatalytic performance owing to the inherent complexity.Here,a strain engineering methodology is proposed to design transition-metal-based HEM by Li manipulation(LiTM)with tunable lattice strain,thus tailoring the electronic structure and boosting electrocatalytic performance.As confirmed by the experiments and calculation results,tensile strain in the LiTM after Li manipulation can optimize the d-band center and increase the electrical conductivity.Accordingly,the asprepared LiTM-25 demonstrates optimized oxygen evolution reaction and hydrogen evolution reaction activity in alkaline saline water,requiring ultralow overpotentials of 265 and 42 mV at 10 mA cm−2,respectively.More strikingly,LiTM-25 retains 94.6%activity after 80 h of a durability test when assembled as an anion-exchange membrane water electrolyzer.Finally,in order to show the general efficacy of strain engineering,we incorporate Li into electrocatalysts with higher entropies as well.

Ultrafine nano-scale Cu_(2)Sb alloy confined in three-dimensional porous carbon as an anode for sodium-ion and potassium-ion batteries

Ultrafine nano-scale Cu2Sb alloy confined in a three-dimensional porous carbon was synthesized using NaCl template-assisted vacuum freeze-drying followed by high-temperature sintering and was evaluated as an anode for sodium-ion batteries(SIBs)and potassium-ion batteries(PIBs).The alloy exerts excellent cycling durability(the capacity can be maintained at 328.3 mA·h·g^(-1) after 100 cycles for SIBs and 260 mA·h·g^(-1) for PIBs)and rate capability(199 mA·h·g^(-1) at 5 A·g^(-1) for SIBs and 148 mA·h·g^(-1) at 5 A·g^(-1) for PIBs)because of the smooth electron transport path,fast Na/K ion diffusion rate,and restricted volume changes from the synergistic effect of three-dimensional porous carbon networks and the ultrafine bimetallic nanoalloy.This study provides an ingenious design route and a simple preparation method toward exploring a high-property electrode for K-ion and Na-ion batteries,and it also introduces broad application prospects for other electrochemical applications.

Approaching High-Performance Lithium Storage Materials by Constructing Hierarchical CoNiO_(2)@CeO_(2)Nanosheets

In this work,the hierarchical CoNiO_(2)@CeO_(2)nanosheet composites were successfully prepared by a one-step hydrothermal process with a subsequent annealing process for the first time.The CeO_(2)nanoparticles successfully deposit on the surface of CoNiO_(2)nanosheet,and benefit the improvement of electrical contact between CoNiO_(2)and CeO_(2).CeO_(2)modification improve the reversibility of insertion/extraction of Li-ions and electrochemical reaction activity,and promotes the transport of Li-ions.Benefited of the unique architecture and component,the CoNiO_(2)@CeO_(2)nanosheet composites show high-reversible capacities,excellent cycling stability and good rate capability.The CoNiO_(2)@CeO_(2)(5.0 wt%)shows a charge/discharge capacity of 867.1/843.2 m Ah g^(-1)after 600 cycles at 1 A g^(-1),but the pristine CoNiO_(2)@CeO_(2)nanosheet only delivers a charge/discharge capacity of 516.9/517.6 m Ah g^(-1)after 500 cycles.The first-principles calculation reveals that valid interfaces between CeO_(2)and NiCoO_(2)can be formed,and the formation process of the interfaces is exothermic.The strong interfacial interaction resulting in an excellent structure stability and thus a cycling stability of the CoNiO_(2)@CeO_(2)material.This work provides an effective strategy to develop highperformance anode materials for advanced a lithium-ion battery,and the CoNiO_(2)@CeO_(2)nanosheet shows a sizeable potential as an anode material for next generation of high-energy Li-ion batteries.

Approaching high-performance lithium storage materials by constructing Li_(2)ZnTi_(3)O_(8)@LiAlO_(2) composites

The Li_(2)ZnTi_(3)O_(8)@Li AlO_(2)was synthesized by a facile high-temperature solid-state route.The LiAlO_(2)modification does not alter the morphology and particle size of Li_(2)Zn Ti_(3)O_(8)(LZTO).The LiAlO_(2)modification improves the structure stability,intercalation/deintercalation reversibility of lithium-ions,and electrochemical reaction activity of Li_(2)Zn Ti_(3)O_(8),and promotes the transfer of lithium ions.Benefited from the unique component,Li_(2)Zn Ti_(3)O_(8)@Li AlO_(2)(8wt%) shows a good rate performance with charge capacities of 203.9,194.8,187.4,180.6,and177.1 mAh·g^(-1)at 0.5,1,2,3,and 5 C,respectively.Nevertheless,pure LZTO only delivers charge capacities of 134.5,109.7,89.4,79.9,and 72.9 mAh·g^(-1)at the corresponding rates.Even at large charge–discharge rate,the Li_(2)Zn Ti_(3)O_(8)@Li AlO_(2)(8wt%) composite indicates a good cycle performance with a high reversible charge/discharge capacity of 263.5/265.8 mAh·g^(-1)at 5 C after 150 cycles.The introduction of LiAlO_(2)on the surface of Li_(2)Zn Ti_(3)O_(8)enhances electronic conductivity of the composite,resulting in the good electrochemical performance of Li_(2)Zn Ti_(3)O_(8)@Li AlO_(2)composite.Li_(2)Zn Ti_(3)O_(8)@LiAlO_(2)(8wt%) composite shows a good potential as an anode material for the next generation of high-performance Li-ion batteries.

利用NH_(4)Cl焙烧-水浸工艺从低冰镍中提取金属并合成(Ni,Cu,Co)Fe_(2)O_(4)光催化剂

针对低冰Ni火法冶炼过程能耗高、Co损失大的问题,本文提出了NH_(4)Cl焙烧-水浸联合提取金属,再分离利用金属的工艺。通过正交试验,研究了NH_(4)Cl焙烧过程中不同因素对金属提取的影响,并确定了优化的工艺条件。结果表明,焙烧温度和NH_(4)Cl用量为主要的影响因素,最佳氯化条件为:低冰镍粒径<75μm,焙烧温度500℃,焙烧时间2.5 h,NH_(4)Cl用量250%,O_(2)流速20 mL/min。通过研究温度和时间对金属浸出的影响,确定了适宜的浸出条件为:温度90℃,时间2 h,这时Ni、Cu、Co和Fe的浸出率分别达到97.6%、96.2%、94.5%和29.2%。以浸出液为原料,以α-Fe_(2)O_(3)为载体与其他金属复合,合成了(Ni,Cu,Co)Fe_(2)O_(4)光催化剂。最佳制备条件确定为:沉淀温度25℃,Ni-Cu-Co与Fe的摩尔比1:3。制备的催化剂为40~60 nm的球形纳米颗粒,在120 min内对亚甲基蓝溶液的降解率可达99.8%。

Rapid lithium-ion insertion/extraction and migration behavior of Na_(2)WO_(4)-encapsulated lithium-rich layered oxide cathode

Due to the low cost,high working voltage and high storage capacity,Li-rich Mn-based layered compounds show promise as the cathode materials for lithiumion batteries(LIBs).However,the side reactions at the solid-liquid interface of the cathode will lead to rapid capacity decay and inferior rate performance.Herein,this article proposes a liquid-phase dispersion strategy to introduce a Na_(2)WO_(4)layer on the Li_(1.2)Ni_(0.13)-Co_(0.13)Mn_(0.54)O_(2) cathode,which can reduce the side effects between raw materials and electrolyte and promote the insertion/extraction rate of Li^(+),thus enhancing the material stability and rate performance.As a result,the capacity retention rate is 96.9%after 200 cycles under 2C.Moreover,the capacities are 177.5,149.5,111.1 and58.3 mAh·g^(-1)at 1C,2C,5C and 10C,implying a superior fast charging performance.The exceptional performance can be ascribed to both the increased conductivity and enhanced structural stability of the cathode material.What's more,based on the investigation of ion insertion/extraction behavior in electrode materials and the ion migration kinetics in the electrolyte,this study suggests that coating Li-rich Mn-based materials with Na_(2)WO_(4)can be a promising strategy to improve their performance in LIBs.