An efficient Hauser-base electrolyte for rechargeable magnesium batteries

Rechargeable magnesium batteries(RMBs)are considered the promising candidates for post lithium-ion batteries due to the abundant storage,high capacity,and dendrite-rare characteristic of Mg anode.However,the lack of practical electrolytes impedes the development and application of RMBs.Here,through a one-step reaction of LiCl congenital-containing Knochel–Hauser base TMPL(2,2,6,6-tetrame thylpiperidinylmagnesium chloride lithium chloride complex)with Lewis acid AlCl_(3),we successfully synthesized an efficient amino-magnesium halide TMPLA electrolyte.Raman and mass spectroscopy identified that the electrolyte comprises the typical di-nuclear copolymer[Mg_(2)Cl_(3)·6THF]+cation group and[(TMP)2AlCl_(2)]-anion group,further supported by the results of density functional theory calculations(DFT)and the Molecular dynamics(MD)simulations.The TMPLA electrolyte exhibits promising electrochemical performance,including available anodic stability(>2.65 V vs.SS),high ionic conductivity(6.05mS cm^(-1)),and low overpotential(<0.1 V)as well as appropriate Coulombic efficiency(97.3%)for Mg plating/stripping.Both the insertion Mo6S8cathode and conversion Cu S cathode delivered a desirable electrochemical performance with high capacity and good cycling stability based on the TMPLA electrolyte.In particular,when compatible with low cost and easily synthesized Cu S,the Cu S||Mg cell displayed an extremely high discharge capacity of 458.8 mAh g^(-1)for the first cycle and stabilized at 170.2 mAh g^(-1)with high Coulombic efficiency(99.1%)after 50 cycles at 0.05 C.Our work proposes an efficient electrolyte with impressive compatibility with Mg anode and insertion/conversion cathode for practical RMBs and provides a more profound knowledge of the Lewis acid–base reaction mechanisms.

Bi nanoparticles encapsulated in nitrogen-doped carbon as a long-life anode material for magnesium batteries

Bismuth has garnered significant interest as an anode material for magnesium batteries(MBs) because of its high volumetric specific capacity and low working potential. Nonetheless, the limited cycling performance(≤100 cycles) limits the practical application of Bi as anode for MBs. Therefore, the improvement of Bi cycling performance is of great significance to the development of MBs and is also full of challenges. Here, Bi nanoparticles encapsulated in nitrogen-doped carbon with single-atom Bi embedded(Bi@NC) are prepared and reported as an anode material for MBs. Bi@NC demonstrates impressive performance, with a high discharge capacity of 347.5 mAh g^(-1) and good rate capability(206.4 mAh g^(-1)@500 mA g^(-1)) in a fluoride alkyl magnesium salt electrolyte. In addition, Bi@NC exhibits exceptional long-term stability, enduring 400 cycles at 500 mA g^(-1). To the best of our knowledge, among reported Bi and Bi-based compounds for MBs, Bi@NC exhibits the longest cycle life in this work. The magnesium storage mechanism of Bi@NC is deeply studied through X-ray diffraction, transmission electron microscopy and X-ray photoelectron spectroscopy. This work provides some guidance for further improving the cycling performance of other alloy anodes in MBs.

Porous polymer electrolytes for long-cycle stable quasi-solid-state magnesium batteries

The development of applicable electrolytes is the key point for high-performance rechargeable magnesium batteries(RMBs).The use of liquid electrolyte is prone to safety problems caused by liquid electrolyte leakage.Polymer-based gel electrolytes with high ionic conductivity,great flexibility,easy processing,and high safety have been studied by many scholars in recent years.In this work,a novel porous poly(vinylidene fluoride-co-hexafluoropropylene)(PVDF-HFP)membrane is prepared by a phase inversion method.By immersing porous PVDF-HFP membranes in MgCl2-AlCl3/TEGDME(Tetraethylene glycol dimethyl ether)electrolytes,porous PVDF-HFP based electrolytes(PPEs)are formed.The PPE exhibits a high ionic conductivity(4.72×10^(-4) S cm-1,25℃),a high liquid electrolyte uptake of 162%,as well as a wide voltage window(3.1 V).The galvanostatic cycling test of Mg//Mg symmetric cell with PPE reveals that the reversible magnesium ion(Mg^(2+))plating/stripping occurs at low overpotentials(~0.13 V).Excellent long cycle stability(65.5 mAh g^(-1) over 1700 cycles)is achieved for the quasisolid-state RMB assembled with MoS2/C cathode and Mg anode.Compared with the liquid electrolyte,the PPE could effectively reduce the side reactions and make Mg^(2+)plating/stripping more uniformly on the Mg electrode side.This strategy herein provides a new route to fabricate high-performance RMB through suitable cathode material and polymer electrolyte with excellent performance.

High-rate performance magnesium batteries achieved by direct growth of honeycomb-like V_(2)O_(5)electrodes with rich oxygen vacancies

Rechargeable magnesium batteries(RMBs)have emerged as a promising next-generation electrochemical energy storage technology due to their superiority of low price and high safety.However,the practical applications of RMBs are severely limited by immature electrode materials.Especially,the high-rate cathode materials are highly desired.Herein,we propose a dualfunctional design of V_(2)O_(5)electrode with rational honeycomb-like structure and rich oxygen vacancies to enhance the kinetics synergistically.The result demonstrates that oxygen vacancies can not only boost the intrinsic electronic conductivity of V_(2)O_(5),but also enhance the Mg^(2+)diffusion kinetics inside the cathode,leading to the good high-rate performance.Moreover,ex-situ X-ray diffraction(XRD),transmission electron microscopy(TEM),and X-ray photoelectron spectroscopy(XPS)characterizations reveal that Mg^(2+)is mainly intercalated from the(101)plane of V_(2)O_(5)−X based on the insertion-type electrochemical mechanism;meanwhile,the highly reversible structure evolution during Mg^(2+)insertion/extraction is also verified.This work proposes that the dual-functional design of electrode has a great influence in enhancing the electrochemical performance of cathode materials for RMBs.

Boosting the cycling stability of rechargeable magnesium batteries by regulating the compatibility between nanostructural metal sulfide cathodes and non-nucleophilic electrolytes

Rechargeable magnesium batteries are attractive candidates for energy storage due to their high theoretical specific capacities,free of dendrite formation and natural abundance of magnesium.However,the development of magnesium secondary batteries is severely limited by the lack of high-performance cathode materials and the incompatibility of electrode materials with electrolytes.Herein,we report the application of CuS nanoflower cathode material based on the conversion reaction mechanism for highly reversible magnesium batteries with boosted electrochemical performances by adjusting the compatibility between the cathode and electrolyte.By applying non-nucleophilic electrolytes based on magnesium bis(hexamethyldisilazide)and magnesium chloride dissolved in the mixed solvent of tetrahydrofuran and N-butyl-N-methyl-piperidinium bis((trifluoromethyl)sulfonyl)imide(Mg(HMDS)_(2)-MgCl_(2)/THF-PP14TFSI)or magnesium bis(trifluoromethanesulfonyl)imide,magnesium chloride and aluminium chloride dissolved in dimethoxyethane(Mg(TFSI)2-MgCl_(2)-AlCl_(3)/DME),the magnesium batteries with CuS nanoflower cathode exhibit a high discharge capacity of~207 mAh·g^(–1)at 100 mA·g^(–1)and a long life span of 1,000 cycles at 500 mA·g^(–1).This work suggests that the rational regulation of compatibility between electrode and electrolyte plays a very important role in improving the performance of multi-valent ion secondary batteries.

Stable multi-electron reaction stimulated by W doping VS_(4)for enhancing magnesium storage performance

Rechargeable magnesium batteries(RMBs)hold promise for offering higher volumetric energy density and safety features,attracting increasing research interest as the next post lithium-ion batteries.Developing high performance cathode material by inducing multi-electron reaction process as well as maintaining structural stability is the key to the development and application of RMBs.Herein,multielectron reaction occurred in VS_(4)by simple W doping strategy.W doping induces valence of partial V as V^(2+)and V^(3+)in VS_(4)structure,and then stimulates electrochemical reaction involving multi-electrons in 0.5%W-V-S.The flower-like microsphere morphology as well as rich S vacancies is also modulated by W doping to neutralize structure change in such multi-electron reaction process.The fabricated 0.5%W-V-S delivers higher specific capacity(149.3 m A h g^(-1)at 50 m A g^(-1),which is 1.6 times higher than that of VS_(4)),superior rate capability(76 mA h g^(-1)at 1000 mA g^(-1)),and stable cycling performance(1500cycles with capacity retention ratio of 93.8%).Besides that,pesudocapaticance-like contribution analysis as well as galvanostatic intermittent titration technique(GITT)further confirms the enhanced Mg^(2+)storage kinetics during such multi-electron involved electrochemical reaction process.Such discovery provides new insights into the designing of multi-electron reaction process in cathode as well as neutralizing structural change during such reaction for realizing superior electrochemical performance in energy storage devices.

Low-temperatures synthesis of CuS nanospheres as cathode material for magnesium second batteries

Rechargeable magnesium batteries(RMBs),as one of the most promising candidates for efficient energy storage devices with high energy,power density and high safety,have attracted increasing attention.However,searching for suitable cathode materials with fast diffusion kinetics and exploring their magnesium storage mechanisms remains a great challenge.Cu S submicron spheres,made by a facile low-temperature synthesis strategy,were applied as the high-performance cathode for RMBs in this work,which can deliver a high specific capacity of 396mAh g^(-1)at 20 mA g^(-1) and a remarkable rate capacity of 250 m Ah g^(-1)at 1000 mA g^(-1).The excellent rate performance can be assigned to the nano needle-like particles on the surface of Cu S submicron spheres,which can facilitate the diffusion kinetics of Mg^(2+).Further storage mechanism investigations illustrate that the Cu S cathodes experience a two-step conversion reaction controlled by diffusion during the electrochemical reaction process.This work could make a contribution to the study of the enhancement of diffusion kinetics of Mg2+and the reaction mechanism of RMBs.

A critical review of vanadium-based electrode materials for rechargeable magnesium batteries

Rechargeable magnesium batteries(RMBs)are one of the most promising next-generation energy storage devices due to their high safety and low cost.With a large family and versatile advantageous structures,vanadium-based compounds are highly competitive as electrode materials of RMBs.This review summa-rizes the structural characteristics,electrochemical performance,and refinement methods of vanadium-based materials,including vanadium oxides,vanadium sulfides,vanadates,vanadium phosphates,and vanadium spinel compounds,as RMB cathodes.Although relatively less,vanadium-based materials as RMB anodes are also introduced.According to the application requirements of RMBs,present common strategies are concluded to improve the electrochemical performance of vanadium-based materials;the probably promising development directions are also proposed,which are not limited only to the elec-trode materials,but also the compatible electrolytes and separator materials.In the near future,RMBs are expected from their large-scale application,standing at the forefront of the energy storage era.

Hybrid solid electrolyte interphases formed in conventional carbonate electrolyte enable high-voltage and ultra-stable magnesium metal batteries

Magnesium metal batteries are considered as viable alternatives of lithium-ion batteries for their low cost and high capacity of magnesium.Nevertheless,the practical application of magnesium metal batteries is extremely challenging due to a lack of suitable electrolyte that can stabilize magnesium metal anode and high-voltage cathode simultaneously.Herein,we found that in-situ formed lithium/magnesium hybrid electrolyte interphases in conventional LiPF6-containing carbonate-based electrolyte can not only prevent the production of passivation layer on the magnesium metal anode,but also inhibit the oxidation of the electrolyte under high voltage.The symmetric magnesium‖magnesium battery can achieve reversible stripping/plating for 1600 and 600 h at 0.02 and 0.1 mA cm^(-2),respectively.In addition,when coupled with a carbon fiber cathode,the magnesium metal battery exhibited a capacity retention rate of 96.3% for 1000 cycles at a current density of 500 mA g^(-1)and presented a working voltage of ~3.1 V.This research paves a new and promising path to the commercialization process of rechargeable magnesium metal batteries.

Recent progress on selenium-based cathode materials for rechargeable magnesium batteries: A mini review

Rechargeable magnesium batteries have received increasing interest because of the prominent advantages, including high security, low cost, and high energy density. The development of rechargeable magnesium batteries is hindered by the sluggish Mg2+ion diffusion kinetics, which makes the exploration of high-performance cathode materials a problem. Recently researchers have exploited various seleniumbased cathodes for rechargeable magnesium batteries. Herein, we have critically reviewed these advancements, studying different types of reaction mechanisms and analyzing the electrochemical performance of cathode materials in rechargeable magnesium batteries. Besides, as key materials for rechargeable magnesium batteries, the exploit and optimization of electrolytes are discussed as well, including the selection of reagents, the effect of Li salts, and the compatibility between electrodes and electrolytes. Finally,promising directions are proposed for future rechargeable magnesium batteries based on selenium-based cathode materials.

The design of Co_(3)S_(4)@MXene heterostructure as sulfur host to promote the electrochemical kinetics for reversible magnesium-sulfur batteries

The rechargeable Mg-S batteries are attractive because of their resource abundances of Mg and S,high volumetric energy density,and less dendrite property of Mg anodes.However,the development is barred by the intrinsic low electronic conductivity of S and the discharge products as well as the lack of understanding the hidden electrochemical kinetics.Here,a Co_(3)S_(4)@MXene heterostructure is proposed as effective sulfur host for reversible Mg-S batteries.XPS results and density functional theory(DFT)calculation confirm that the chemical interaction between the decorated Co_(3)S_(4)nanocrystals host and polysulfide intermediates could well absorb and catalyze the polysulfides conversion,thus improve the electrochemical redox kinetics.Meanwhile,the MXene matrix could promote Mg ion diffusion dynamics greatly.As a result,the developed Mg-S batteries using the Co_(3)S_(4)@MXene-S as the cathode material could demonstrate high sulfur utilization with specific capacity of 1220 mAh g^(-1) and retain a capacity of 528 mAh g^(-1) after 100 cycles,together with a satisfactory rate performance even at 2 C.This work shed light on the advanced cathode design for reversible high energy Mg-S batteries.

A rapid solid-state synthesis of electrochemically active Chevrel phases （Mo6T8; T = S, Se） for rechargeable magnesium batteries

High energy mechanical milling （HEMM） of a stoichiometric mixture of molybdenum and metal chalcogenides （CuT and MOT2; T = S, Se） followed by heat treatment at elevated temperatures was successfully applied to synthesize Chevrel phases （Cu2Mo6T8; T = S, Se） as positive electrodes for rechargeable magnesium batteries. Differential scanning calorimetry （DSC）, thermogravimetric analyses （TGA）, X-ray diffraction （XRD）, and scanning electron microscopy （SEM） were used to understand the phase formation following milling and heat treatment. CuS and Mo were observed to react at 714-800 K and formed an intermediate ternary Chevrel phase （Cu1.83Mo3S4）, which further reacted with residual Mo and MoS2 to form the desired Cu2MosSs. Quantitative XRD analysis shows the formation of a -96%-98% Chevrel phase at 30 min following the milling and heat treatment. The electrochemical performance of de-cuprated Mo6S8 and Mo6Ses phases were evaluated by cyclic voltammetry （CV）, galvanostatic cycling, and electrochemical impedance spectroscopy （EIS）. The results of the CV and galvanostatic cycling data showed the expected anodic/cathodic behavior and a stable capacity after the first cycle with the formation of MgxMo6T8 （T = S, Se; 1 ≤ x 〈 2）. EIS at -0.1 V intervals for the Mo6Ss electrode during the first and second cycle shows that partial Mg-ion trapping resulted in an increase in charge transfer resistance Re. In contrast, the interfacial resistance Ri remained constant, and no significant trapping was evident during the galvanostatic cycling of the Mo6,Se8 electrode. Importantly, the ease of preparation, stable capacity, high Coulombic efficient35 and excellent rate capabilities render HEMM a viable route to laboratory-scale production of Chevrel phases for use as positive electrodes for rechargeable magnesium batteries.

Origin of Excellent Charge Storage Properties of Defective Tin Disulphide in Magnesium/Lithium-Ion Hybrid Batteries

Lithium-ion batteries(LIBs)are excellent electrochemical energy sources,albeit with existing challenges,including high costs and safety concerns.Magnesium-ion batteries(MIBs)are one of the potential alternatives.However,the performance of MIBs is poor due to their sluggish solid-state Mg^(2+) diffusion kinetics and severe electrode polarizability.Rechargeable magnesium-ion/lithium-ion(Mg^(2+)/Li^(+))hybrid batteries(MLHBs)with Mg^(2+) and Li+as the charge carriers create a synergy between LIBs and MIBs with significantly improved charge transport kinetics and reliable safety features.However,MLHBs are yet to reach a reasonable electrochemical performance as expected.This work reports a composite electrode material with highly defective two-dimensional(2D)tin sulphide nanosheets(SnS_(x))encapsulated in three-dimensional(3D)holey graphene foams(HGF)(SnS_(x)/HGF),which exhibits a specific capacity as high as 600 mAh g^(−1) at 50 mA g^(−1) and a compelling specific energy density of~330 Wh kg^(−1).The excellent electrochemical performance surpasses previously reported hybrid battery systems based on intercalation-type cathode materials under comparable conditions.The role played by the defects in the SnS_(x)/HGF composite is studied to understand the origin of the observed excellent electrochemical performance.It is found that it is closely related to the defect structure in SnS_(x),which offers percolation pathways for efficient ion transport and increased internal surface area assessable to the charge carriers.The defective sites also absorb structural stress caused by Mg^(2+) and Li+insertion.This work is an important step towards realizing high-capacity cathode materials with fast charge transport kinetics for hybrid batteries.

Multidimensional defects tailoring local electron and Mg^(2+) diffusion channels for boosting magnesium storage performance of WO_(3)/MoO_(2)

Defect engineering presents great promise in addressing lower specific capacity,sluggish diffusion kinetics and poor cycling life issues in energy storage devices.Herein,multidimensional(0D/2D/3D) structural defects are constructed in WO_(3)/MoO_(2) simultaneously via competing for and sharing with O atoms during simple hydrothermal process.OD and 2D defects tailor local electron,activating more sites and generating built-in electric fields to yield ion reservoir,meanwhile,3D defect owning lower anisotropic property tailors Mg^(2+) diffusion channels to fully exploit Mg^(2+) adsorbed sites induced by OD and 2D defects,enhance the kinetics and maintain structural stability.Benefitted from synergistic effect of 0D/2D/3D structural defects,the designed WO_(3)/MoO_(2) shows the higher specific capacity(112.8 mA h g^(-1) at 50 mA g^(-1) with average attenuation rate per cycle of 0.068%),superior rate capability and excellent cycling stability(specific capacity retention of 80% after 1500 cycles at 1000 mA g^(-1)).This strategy provides design ideas of introducing multidimensional structural defects for tailoring local electron and microstructure to improve energy storage property.

Reversible Magnesium Metal Anode Enabled by Cooperative Solvation/Surface Engineering in Carbonate Electrolytes

Magnesium metal anode holds great potentials toward future high energy and safe rechargeable magnesium battery technology due to its divalent redox and dendrite-free nature. Electrolytes based on Lewis acid chemistry enable the reversible Mg plating/stripping,while they fail to match most cathode materials toward highvoltage magnesium batteries. Herein,reversible Mg plating/stripping is achieved in conventional carbonate electrolytes enabled by the cooperative solvation/surface engineering. Strongly electronegative Cl from the MgCl_(2) additive of electrolyte impairs the Mg…O = C interaction to reduce the Mg^(2+) desolvation barrier for accelerated redox kinetics,while the Mg^(2+)-conducting polymer coating on the Mg surface ensures the facile Mg^(2+) migration and the e ective isolation of electrolytes. As a result,reversible plating and stripping of Mg is demonstrated with a low overpotential of 0.7 V up to 2000 cycles. Moreover,benefitting from the wide electrochemical window of carbonate electrolytes,high-voltage(> 2.0 V) rechargeable magnesium batteries are achieved through assembling the electrode couple of Mg metal anode and Prussian blue-based cathodes. The present work provides a cooperative engineering strategy to promote the application of magnesium anode in carbonate electrolytes toward high energy rechargeable batteries.

High area-capacity Mg batteries enabled by sulfur/copper integrated cathode design

Rechargeable Mg batteries potentially display lower cost and competitive energy density compared with their Li-ion counterparts.However,the practical implementation of high area-capacity cathodes still remains a formidably challenging task.This work presents the sulfur/copper integrated cathodes fabricated by the conventional blade-coating process and slurry-dipping method.The sulfur/copper foil integrated cathodes deliver a high area-capacity of 2.6 mAh cm^(-2)after 40 cycles,while the sulfur/copperfoam integrated cathode exhibits an ultrahigh area-capacity of 35.4 mAh cm^(-2),corresponding to 743.1 Wh L^(-1)at the electrode level(1.5 times higher than the LiCoO_(2)-graphite system).The in-situ formed copper sulfide intermediates with sufficient cation defects can act as functional intermediates to regulate the sulfur electrochemistry during the first discharge process.The subsequent cycles are operated by the reversible displacement reaction between Mg-ions and copper sulfide active substances.In particular,the copper ions prefer to extrude along the[001]direction in copper sulfides lattice and simultaneously the rock-salt MgS crystals are generated.Besides,the nonuniform surface topography of the cycled Mgmetal anode,caused by the spatial inhomogeneity in current distribution,is demonstrated to lead to the battery performance degradation for high area-capacity Mg batteries.

Mechanisms of electrochemical magnesium(de)alloying of Mg-Sn and Mg-Pb polymorphs

Different polymorphs of Mg-Sn and Mg-Pb intermetallic compounds were prepared by high-energy mechanical alloying and then investigated as active material in magnesium batteries. Beside thermodynamically stable Mg_(2)Sn and Mg_(2)Pb crystallizing in the anti-fluorite structure, other polymorphs Mg_(~2)Sn and Mg_(~2)Pb were prepared by increasing the ball-milling time. The first dealloying process is almost complete only for the cubic polymorphs, then similar capacities are observed during the subsequent alloying and dealloying sequences.Thanks to operando X-ray diffraction, the electrochemical mechanism is revealed and shows that the cubic polymorphs Mg_(2)Sn and Mg_(2)Pb tend to preferentially form during the alloying whatever the pristine intermetallic. Weak traces of Mg_(~2)Sn and Mg_(~2)Pb are observed during the alloying, suggesting that these polymorphs act as a by-product and/or an intermediate phases of the electrochemical process. Finally, the compatibility of cubic Mg_(2)Sn and Mg_(2)Pb with Mg(TFSI)_(2)-based electrolyte is confirmed in full cell vs. a positive electrode based on the Chevrel phase Mo6S8, although limited performance is achieved. This fundamental work provides new insights in the behavior of alloy-type negative electrodes for magnesium-ion batteries.

Rechargeable metal(Li, Na, Mg, Al)-sulfur batteries: Materials and advances

Energy and environmental issues are becoming more and more severe and renewable energy storage technologies are vital to solve the problem.Rechargeable metal(Li,Na,Mg,Al)-sulfur batteries with low-cost and earth-abundant elemental sulfur as the cathode are attracting more and more interest for electrical energy storage in recent years.Lithium-sulfur(Li-S),room-temperature sodium-sulfur(RT Na-S),magnesium-sulfur(Mg-S)and aluminum-sulfur(Al-S)batteries are the most prominent candidates among them.Many obvious obstacles are hampering the developments of metal-sulfur batteries.Li-S and Na-S batteries are encumbered mainly by anode dendrite issues,polysulfides shuttle and low conductivity of cathodes.Mg-S and Al-S batteries are short of suitable electrolytes.In this review,relationships between various employed nanostructured materials and electrochemical performances of metal-sulfur batteries have been demonstrated.Moreover,the selections of suitable electrolytes,anode protection,separator modifications and prototype innovations are all crucial to the developments of metal-sulfur batteries and are discussed at the same time.Herein,we give a review on the advances of Li-S,RT Na-S,Mg-S and Al-S batteries from the point of view of materials,and then focus on perspectives of their future developments.

Emerging rechargeable aqueous magnesium ion battery

Recently,aqueous rechargeable batteries have played an essential role in developing renewable energy due to the merits of low cost,high security,and high energy density.Among various aqueous-based batteries,aqueous magnesium ion batteries(AMIBs)have rich reserves and high theoretical specific capacity(3833 mAh cm3).However,for future industrialization,AMIBs still face many scientific issues to be solved,such as the slow diffusion of magnesium ions in the material structure,the desolvation penalty at electrode-electrolyte interfaces,the cost of water-in-salt electrolyte,the low voltage of traditional aqueous electrolyte,etc.And yet a comprehensive summary of the components of AMIBs is lacking in the research community.This review mainly introduces the exploration and development of AMIB systems and related components.We conduct an in-depth study of the cathode materials appropriate for magnesium ion batteries from their crystal structures,focusing primarily on layered structures,spinel structures,tunnel structures,and three-dimensional framework structures.We also investigate the anode materials,ranging from inorganic materials to organic materials,as well as the electrolyte materials(from the traditional electrolyte to water-in-salt electrolyte).Finally,some perspectives on ensuing optimization design for future research efforts in the AMIBs field are summarized.