Layered buserite Mg-Mn oxide cathode for aqueous rechargeable Mg-ion battery

Owing to the features(high safety,inexpensive and environmental friendliness)of aqueous rechargeable Mg-ion batteries(ARMIBs),they have drawn extensive attention in the future energy storage systems.However,the poor Mg^(2+)migration kinetics during the Mg^(2+)intercalation/extraction still hinders the progress of developing suitable cathode materials.Herein,a layered buserite Mg-Mn oxide(MMO)material with large interlayer space(~9.70A)and low-crystalline structure is studied as a high-performance cathode in ARMIBs.Compared with the counterpart,the Mg^(2+)migration kinetics of the MMO cathode can be enhanced by its unique structure(bigger interlayer spacing and low-crystalline structure).The layered buserite MMO as a high-performance ARMIBs cathode exhibits high Mg storage capacity(50 mAg^(-1):169.3 mAh g^(-1)),excellent rate capability(1000 mAg^(-1):98.3 mAh g^(-1)),and fast Mg^(2+)migration(an average diffusion coefficient:~4.21×10-^(10)cm^(2)s^(-1))in 0.5 M MgCl_(2)aqueous electrolyte.Moreover,the MMO-1//AC full battery achieved a high discharge capacity(100 mAg^(-1):111 mAh g^(-1)),and an ignored fading over 5000 cycles(1000 mAg^(-1)).Therefore,layered Mg-Mn oxide with large interlayer space may break a new path to develop the promising ARMIBs.

Density Functional Theory Calculations for the Evaluation of FePS3 as a Promising Anode for Mg Ion Batteries

FePS3,a classical 2D layered material with transition metal phosphorous trichalcogenides,was investigated as an anode material for Mg ion batteries.We used density functional theory to calculate the Mg storage properties of FePS3,such as Mg adsorption energy,theoretical specific capacity,average voltage,diffusion energy barriers,volume change,and electronic conductivity.The theoretical specific capacity of the FePS3 monolayer is 585.6 mA h/g with a relatively low average voltage of 0.483 V(vs.Mg/Mg^2+),which is favorable to a high energy density.The slight change in volume and good electronic conductivity of bulk FePS 3 are beneficial to electrode stability during cycling.

Adsorption equilibrium, kinetics, and dynamic separation of Ca2+ and Mg2+ ions from phosphoric acid–nitric acid aqueous solution by strong acid cation resin

The separation of Ca2+and Mg2+ions from phosphoric acid-nitric acid aqueous solution is very significant for the neutralization process of nitrophosphate fertilizer.This paper studied the adsorption equilibrium,kinetics,and dynamic separation of Ca2+and Mg2+ions by strong acid cation resin,and the effects of phosphoric acid and nitric acid on the adsorption process were investigated.The results reveal that the adsorption process of Ca2+and Mg2+ions in pure water on resin is in good agreement with the Langmuir isotherm model and their maximal adsorption capacities are 1.86 mmol·g-1 and 1.83 mmol·g-1,respectively.The adsorption kinetics of Ca2+and Mg2+ions on resin fits better with the pseudo-first-order model,and the adsorption equilibrium in pure water is reached within 10 min contact time,while at the present of phosphoric acid,the adsorption rate of Ca2+and Mg2+ions on resin will go down.The dynamic separation experiments demonstrate that the designed column adsorption is able to undertake the separation of metal ions from the mix acids aqueous solution,but the dynamic operation should control the flow rate of mix acid solution.Besides nitric acid solution was proved to be effective to completely regenerate the spent resin and achieve the recyclable operation of separation process.

Shape controllable synthesis and enhanced upconversion photoluminescence ofβ-NaGdF4:Yb^3+,Er^3+nanocrystals by introducing Mg(^2+)

Different concentrations of Mg^（2＋） -doped hexagonal phase NaGdF_4：Yb^（3＋）, Er^（3＋）nanocrystals（NCs） were synthesized by a modified solvothermal method. Successful codoping of Mg^（2＋）ions in upconversion nanoparticles（UCNPs） was supported by XRD, SEM, EDS, and PL analyses. The effects of Mg^（2＋）doping on the morphology and the intensity of the upconversion（UC） emission were discussed in detail. It turned out that with the concentration of Mg^（2＋）increasing, the morphology of the nanoparticles turn to change gradually and the UC emission was increasing gradually as well. Notably the UC fluorescence intensities of Er^（3＋）were gradually improved owing to the codoped Mg^（2＋）and then achieved a maximum level as the concentration of Mg^（2＋）ions was 60 mol% from the amendment of the crystal structure of β-NaGdF_4：Yb^（3＋）,Er^（3＋）nanoparticles. Moreover, the UC luminescence properties of the rare-earth（Yb3＋, Er^（3＋）） ions codoped NaGdF_4 nanocrystals were investigated in detail under 980-nm excitation.

Understanding the low temperature electrochemistry of magnesium-lithium hybrid ion battery in all-phenyl-complex solutions

Magnesium-lithium hybrid ion batteries have emerged as a new class of energy storage systems owing to dendrite free cycling of magnesium anode and possibility of practice of numerous conventional lithium cathodes.In present work,we used hybrid ion strategy to analyze the performance of lithium titanate based lithium cathode,magnesium metal anode,and all-phenyl complex(APC)electrolytes at different temperatures(25℃,10℃,0℃,-10℃,and-20℃).The hybrid ion battery exhibited excellent rate performance(228 m Ah g^(-1)/20 m A g^(-1) and 163 mAh g^(-1)/1000 mA g^(-1))with stable voltage plateaus at 0.90 and 0.75 V,which corresponds to specific energy of 178 Wh kg^(-1) at room temperature(25℃).Experimental results revealed that APC-THF solutions have strong potential to suppress the freezing of electrolyte solutions owing to low boiling point of THF.The low temperature electrochemical testing revealed the reversible capacities of 213.4,165.5,143.8,133.2 and 78.56 mAh g^(-1) at 25,10,0,-10,and-20℃,respectively.Furthermore,ex-situ XRD,SEM,and EIS tests were carried out to understand the reaction kinetics of both Mg2+and Li+ions inside the lithium titanate cathode.We hope this work will shed light on low temperature prospective of electrochemical devices for use in cold environments.

Dealloying induced nanoporosity evolution of less noble metals in Mg ion batteries

Rechargeable Mg ion batteries(MIBs)have aroused great interests,and using alloy-type anodes and conventional electrolytes offers an effective way to develop high energy density Mg battery systems.However,the dealloying-induced nanoporosity evolution of alloy-type anodes during the charging process has received less attention.Herein,using a magnetron-sputtered Mg;Bi;film as an example,we investigate its electrochemical dealloying and associated structural evolution in an all-phenyl-complex electrolyte by in-situ and ex-situ characterizations.The microstructures and length scales of nanoporous Bi can be facilely regulated by changing electrochemical parameters,and there exists a good linear correlation between the surface diffusivity of Bi and the applied current density/potential scan rate on a logarithm scale.More importantly,the self-supporting nanoporous Bi electrodes deliver satisfactory Mg storage performance and alloy-type anodes show good compatibility with conventional electrolytes.Furthermore,the charging-induced dealloying in MIBs is a general strategy to fabricate nanoporous less noble metals like Sn,Pb,In,Cu,Zn and Al,which shows advantages over chemical dealloying in aqueous solutions.Our findings highlight the significance of nanoporosity evolution of alloy-type anodes during dealloying,and open opportunities for the fabrication of nanoporous reactive metals.

Lithium Ion Extraction from the High Ration Mg/Li Salt Lake Brine with Ionic Liquid in Triisobutyl Phosphate and Kerosene

1 Introduction As the lightest metal with the unique properties of energy production and storage,lithium is regarded as the new century energy metal.Lithium and its compounds were widely used in various industrial fields,especially in

Is proton a charge carrier for δ-MnO_(2) cathode in aqueous rechargeable magnesium-ion batteries?

Manganese dioxide(MnO_(2)) is considered as a potential cathode material for aqueous magnesium-ion batteries. However, the charge/discharge mechanism of MnO_(2)in aqueous electrolyte is still unclear. In present study, highly porous δ-MnO_(2) is investigated, which delivers a high capacity of 252.1 m Ah g^(-1) at 0.05 A g^(-1) and excellent rate capability, i.e., 109.7 m Ah g^(-1) at 1 A g^(-1), but a low-capacity retention of 54.4% after 800 cycles at 1 A g^(-1). The two-step discharging process, namely a consequent H^(+) and Mg^(2+) insertion reaction, is verified, by comparing the electrochemical performance of δ-MnO_(2) in 1 M MgCl_(2) and 1 M MnCl_(2) aqueous electrolyte and analyzing detailedly the Mg content and the bonding state of Mn at different charge/discharge state. Furthermore, partial irreversibility of Mg^(-1) ion insertion/extraction is observed, which may be one of the major reasons leading to capacity decay.

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.

On the bramble way to Mg metal anodes in secondary Mg ion batteries

As a prospective alternative to lithium-ion batteries,rechargeable magnesium metal batteries(RMBs)have many unparalleled advantages,including direct use of Mg metal as the electrode;large nature abundance;intrinsically safe merits;high theoretical volumetric capacity.Nonetheless,there exist a large number of challenges on electrodes for their applications.Among them,surface passivation,uneven deposition/dissolution,and corrosion are critical issues that severely hinder the development of Mg anodes in RMBs.This review gives a specific comprehensive,and in-depth summary of mechanisms relative to these problems.Subsequently,it displays the protection progresses of the Mg metal anode via three-dimensional host nanostructure fabrication,Mg alloys anode design,current collector modification,artificial solid-electrolyte interphase construction,and electrolyte optimization.Finally,future perspectives and outlooks in developing the other blossom of these strategies for rechargeable Mg batteries are also discussed.This overview provides significant guidance for designing and fabricating high-performance Mg metal anodes in secondary Mg batteries and boosting their commercial applications.

High Rate Performance of Aqueous Magnesium-iron-ion Batteries Based on Fe_(2)O_(3)@GH as the Anode

Aqueous Mg-ion batteries(MIBs)are safe,non-toxic and low-cost.Magnesium has a high theoretical specific capacity with its ion radius close to that of lithium.Therefore,aqueous magnesium ion batteries have great research advantages in green energy.To acquire the best electrode materials for aqueous magnesium ion batteries,it is necessary for the structural design in material.Fe_(2)O_(3)is an anode material commonly used in Li-ion battery.However,the nano-cube Fe_(2)O_(3)combined with graphene hydrogels(GH)can be successfully prepared and employed as an anode,which is seldom researched in the aqueous batteries system.The Fe_(2)O_(3)/GH is used as anode in the dual MgSO_(4)+FeSO_(4)aqueous electrolyte,avoiding the irreversible deintercalation of magnesium ions.In addition,the Fe element in anode material can form the Fe^(3+)/Fe^(2+)and Fe^(2+)/Fe^(3+)redox pairs in the MgSO_(4)+FeSO_(4)electrolyte.Thus,the reversible insertion/(de)insertion of magnesium and iron ions into/from the host anode material can be simultaneously achieved.After the initial charge,the anodic structure is changed to be more stable,avoiding the formation of MgO.The Fe_(2)O_(3)/GH demonstrates high rate properties and reversible capacities of 198,151,121,80,75 and 27 mAh g^(−1)at 50,100,200,300,500 and 1000 mA g^(−1)correspondingly.