The advantages of sodium-ion batteries(SIBs)for large-scale energy storage are well known.Among possible anode materials,hard carbon(HC)stands out as the most viable commercial option because of its superior performan...The advantages of sodium-ion batteries(SIBs)for large-scale energy storage are well known.Among possible anode materials,hard carbon(HC)stands out as the most viable commercial option because of its superior performance.However,there is still disagreement regarding the sodium storage mechanism in the low-voltage plateau region of HC anodes,and the structure-performance relationship between its complex multiscale micro/nanostructure and electrochemical behavior remains unclear.This paper summarizes current research progress and the major problems in understanding HC’s microstructure and sodium storage mechanism,and the relationship between them.Findings about a universal sodium storage mechanism in HC,including predictions about micropore-capacity relationships,and the opportunities and challenges for using HC anodes in commercial SIBs are presented.展开更多
Metal-organic frameworks(MOFs)are import-ant as possible energy storage materials.Nitrogen-doped iron-cobalt MOFs were synthesized by a one-pot solvo-thermal method using CoCl_(3)·6H_(2)O and FeCl_(3)·6H_(2)...Metal-organic frameworks(MOFs)are import-ant as possible energy storage materials.Nitrogen-doped iron-cobalt MOFs were synthesized by a one-pot solvo-thermal method using CoCl_(3)·6H_(2)O and FeCl_(3)·6H_(2)O dis-solved in N,N-dimethylformamide,and were converted into Fe-Co embedded in N-doped porous carbon polyhedra by pyrolysis in a nitrogen atmosphere.During pyrolysis,the or-ganic ligands transformed into N-doped porous carbon which improved their structural stability and also their electrical contact with other materials.The Fe and Co are tightly bound together because of their encapsulation by the carbon nitride and are well dispersed in the carbon matrix,and improve the material’s conductivity and stability and provide additional capacity.When used as the anode for lithium-ion batteries,the material gives an initial capacity of up to 2230.7 mAh g^(-1)and a reversible capa-city of 1146.3 mAh g^(-1)is retained after 500 cycles at a current density of 0.5 A g^(-1),making it an excellent candidate for this purpose.展开更多
As an emerging electrochemical energy storage technology,potassium-ion batteries(PIBs),which are considered a“beyond Li-ion”battery system,have attracted tremendous attention due to their potential for providing a h...As an emerging electrochemical energy storage technology,potassium-ion batteries(PIBs),which are considered a“beyond Li-ion”battery system,have attracted tremendous attention due to their potential for providing a high energy density,and having abundant resource,and a low cost.However,their commercialization is hindered by the lack of practical anode materials.Among various reported anodes,conventional carbon materials,including graphite,soft carbon,and hard carbon,have emerged as promising candidates because of their abundance,low cost,high conductivity,and tunable structures.However,these materials have problems such as a low initial Coulombic efficiency,significant volume expansion,and unsatisfactory cyclability and rate performance.Various strategies to solve these have been explored,including optimizing the interlayer spacing,structural design,surface coating,constructing a multifunctional framework,and forming composites.This review provides a comprehensive overview of the recent progress in conventional carbon anodes,highlighting structural design strategies,mechanisms for improving the electrochemical performance,and underscores the critical role of these materials in promoting the practical application of PIBs.展开更多
Transition metal sulfides are considered promising anode materials for sodium-ion batteries(SIBs)due to their high theoretical capacity and low synthesis cost.However,is-sues such as poor cyclic stability and rate per...Transition metal sulfides are considered promising anode materials for sodium-ion batteries(SIBs)due to their high theoretical capacity and low synthesis cost.However,is-sues such as poor cyclic stability and rate performance,arising from volume expansion and structural degradation,remain sig-nificant challenges.We report a novel FeS_(2)/CoS_(2) heterostruc-ture embedded in a 3D carbon aerogel matrix(FeS_(2)/CoS_(2)@C)synthesized by a cross-linking and vulcanization process.The resulting core-shell structure,with bimetallic FeS_(2)/CoS_(2) nano-particles encapsulated in a conductive carbon shell,effectively reduces the adverse effects of volume changes during sodiation/desodiation cycles.The 3D porous carbon network increases both ion and electron diffusion,while preventing agglomeration of the active material and maintaining interface integrity.The FeS_(2)/CoS_(2)@C composite has an outstanding electrochemical performance,including a high specific capacity of 725 mAh g^(-1)at 0.5 A g^(-1)and an exceptional rate capability of 572 mAh g^(-1)at 10 A g^(-1).It also has remarkable cycling stability with no signific-ant capacity decay over 1000 cycles at 5 A g^(-1).展开更多
Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes i...Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes it attractive as an anode of Li-ion batteries.Herein,through a one-pot facile high-temperature annealing route,using SBA15 as the silicon source,and embedding tin dioxide SnO_(2)particles into carbon coated SiO_(x),the mesoporous SiO_(x)-SnO_(2)@C rod composite was prepared and tested as the anode material.The results revealed that the SnO_(2)particles were distributed uniformly in the wall,which could further improve their volume energy densities.The coated carbon plays a role in maintaining structural integrality during lithiation,and the rich mesopores structure can release the expanded volume and enhance Li-ion transfer.At 0.1 A·g^(-1),the gravimetric and volumetric capacities of the composite were as high as 1271 mAh·g^(-1)and 1573 mAh·cm^(-3),respectively.After 200 cycles,the 95%capacity could be retained compared with that upon the 2nd cycle at 0.5 A·g^(-1).And the rod morphology was well kept,except that the diameter of the rod was 3 times larger than its original size after the cell was discharged into 0.01 V.展开更多
Sodium-ion batteries(SIBs)have emerged as a promising contender for next-gener-ation energy storage systems.Hard carbon is re-garded as the most promising anode for commer-cial SIB,however,the large number of defects ...Sodium-ion batteries(SIBs)have emerged as a promising contender for next-gener-ation energy storage systems.Hard carbon is re-garded as the most promising anode for commer-cial SIB,however,the large number of defects on its surface cause irreversible electrolyte consump-tion and an uneven solid electrolyte interphase film.An advanced molecular engineering strategy to coat hard carbon with polycyclic aromatic mo-lecules is reported.Specifically,polystyrene-based carbon microspheres(CSs)were first synthesized and then coated with polycyclic aromatic mo-lecules derived from coal tar pitch by spray-drying and followed by oxidation.Compared to the traditional CVD coating meth-od,this molecular framework strategy has been shown to reduce the number of defects on the surface of CSs without sacrifi-cing internal storage sites and suppressing transport kinetics in hosting the sodium ions.Besides the lower surface defect con-centration,the synthesized hybrid carbon microspheres(HCSs)have a larger grain size and more abundant closed pores,and have a higher reversible sodium storage capacity.A HCS-P-60%electrode has a capacity of 332.3 mAh g^(-1)with an initial Cou-lombic efficiency of 88.5%.It also has a superior rate performance of 246.6 mAh g^(-1)at 2 C and a 95.2%capacity retention after 100 cycles at 0.2 C.This work offers new insights into designing high-performance hard carbon microsphere anodes,advan-cing the commercialization of sodium-ion batteries.展开更多
Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit...Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.展开更多
Biomass-derived hard carbons,usually prepared by pyrolysis,are widely considered the most promising anode materials for sodium-ion bat-teries(SIBs)due to their high capacity,low poten-tial,sustainability,cost-effectiv...Biomass-derived hard carbons,usually prepared by pyrolysis,are widely considered the most promising anode materials for sodium-ion bat-teries(SIBs)due to their high capacity,low poten-tial,sustainability,cost-effectiveness,and environ-mental friendliness.The pyrolysis method affects the microstructure of the material,and ultimately its so-dium storage performance.Our previous work has shown that pyrolysis in a sealed graphite vessel im-proved the sodium storage performance of the car-bon,however the changes in its microstructure and the way this influences the sodium storage are still unclear.A series of hard carbon materials derived from corncobs(CCG-T,where T is the pyrolysis temperature)were pyrolyzed in a sealed graphite vessel at different temperatures.As the pyrolysis temperature increased from 1000 to 1400℃ small carbon domains gradually transformed into long and curved domains.At the same time,a greater number of large open pores with uniform apertures,as well as more closed pores,were formed.With the further increase of pyrolysis temperature to 1600℃,the long and curved domains became longer and straighter,and some closed pores gradually became open.CCG-1400,with abundant closed pores,had a superior SIB performance,with an initial reversible ca-pacity of 320.73 mAh g^(-1) at a current density of 30 mA g^(-1),an initial Coulomb efficiency(ICE)of 84.34%,and a capacity re-tention of 96.70%after 100 cycles.This study provides a method for the precise regulation of the microcrystalline and pore structures of hard carbon materials.展开更多
Solid-state Na metal batteries(SSNBs),known for the low cost,high safety,and high energy density,hold a significant position in the next generation of rechargeable batteries.However,the urgent challenge of poor interf...Solid-state Na metal batteries(SSNBs),known for the low cost,high safety,and high energy density,hold a significant position in the next generation of rechargeable batteries.However,the urgent challenge of poor interfacial contact in solid-state electrolytes has hindered the commercialization of SSNBs.Driven by the concept of intimate electrode-electrolyte interface design,this study employs a combination of sodium-potassium(NaK)alloy and carbon nanotubes to prepare a semi-solid NaK(NKC)anode.Unlike traditional Na anodes,the paintable paste-like NKC anode exhibits superior adhesion and interface compatibility with both current collectors and gel electrolytes,significantly enhancing the physical contact of the electrode-electrolyte interface.Additionally,the filling of SiO_(2) nanoparticles improves the wettability of NaK alloy on gel polymer electrolytes,further achieving a conformal interface contact.Consequently,the overpotential of the NKC symmetric cell is markedly lower than that of the Na symmetric cell when subjected to a long cycle of 300 hrs.The full cell coupled with Na_(3)V_(2)(PO_(4))_(2) cathodes had an initial discharge capacity of 106.8 mAh·g^(-1) with a capacity retention of 89.61%after 300 cycles,and a high discharge capacity of 88.1 mAh·g^(-1) even at a high rate of 10 C.The outstanding electrochemical performance highlights the promising application potential of the NKC electrode.展开更多
A process was proposed to convert and separate selenium and arsenic in copper anode slime(CAS) by low-temperature alkali fusion process.Central composite design was employed to optimize the effective parameters,in whi...A process was proposed to convert and separate selenium and arsenic in copper anode slime(CAS) by low-temperature alkali fusion process.Central composite design was employed to optimize the effective parameters,in which Na OH/CAS mass ratio,fusion temperature and fusion time were selected as variables,and the conversion ratio of selenium and arsenic as responses.Second-order polynomial models of high significance and 3D response surface plots were constructed to show the relationship between the responses and the variables.Optimum area of >90% selenium conversion ratio and >90% arsenic conversion ratio was obtained by the overlaid contours at Na OH/CAS mass ratio of 0.65-0.75,fusion temperature of 803-823 K and fusion time of 20-30 min.The models are validated by experiments in the optimum area,and the results demonstrate that these models are reliable and accurate in predicting the fusion process.展开更多
The application of microwave irradiation for pretreatment of copper anode slime with high nickel content prior to pressure sulfuric acid leaching has been proposed.The microwave-assisted pretreatment is a rapid and ef...The application of microwave irradiation for pretreatment of copper anode slime with high nickel content prior to pressure sulfuric acid leaching has been proposed.The microwave-assisted pretreatment is a rapid and efficient process.Through the technology of microwave assisted pretreatment-pressure leaching of copper anode slime,copper,tellurium,selenium and nickel are almost completely recovered.Under optimal conditions,the leaching efficiencies of copper,tellurium,selenium and nickel are 97.12%,95.97%,95.37% and 93.90%,respectively.The effect of microwave radiation on the temperature of copper anode slime and leaching solution is investigated.It is suggested that the enhancement on the recoveries of copper,tellurium and selenium can be attributed to the temperature gradient which is caused by shallow microwave penetration depth and super heating occurring at the solid–liquid interface.The kinetic study shows that the pressure leaching of copper anode slime,with and without microwave assisted pretreatment,are both controlled by chemical reactions on the surfaces of particles.It is found that the activation energy calculated for microwave-assisted pretreatment-pressure leaching(49.47 kJ/mol) is lower than that for pressure leaching which is without microwave assisted pretreatment(60.57 kJ/mol).展开更多
A study was carried out on kinetics of oxygen evolution on lead alloy anodes in sulphuric acidicelectrolyte. The influence of alloy elements Ca, Ag and Sn on the overpotential of oxygen evolution was investigated. All...A study was carried out on kinetics of oxygen evolution on lead alloy anodes in sulphuric acidicelectrolyte. The influence of alloy elements Ca, Ag and Sn on the overpotential of oxygen evolution was investigated. All anodes had been subjected to a pre-polarization before the measurement of potential-currentcurves for oxygen evolution. The overpotential of oxygen evolution was found to be decreased when the alloyanode contained Ca and Ag, whereas it remained unchanged when the alloy anode contained Sn. For oxygenevolution on lead alloy anodes the TAFEL equation was valid. The b vulue for Ph and Ph-Ca anodes was approx. 100, for Ph-Ag, Ph-Ag-Ca anodes it was approx. 140. The a value for Ph Ca, Ph-Ag, Ph-Ag-Ca anodes decreased with the increase of Ca or/and Ag content. The a and b value was not influenced by Sn in theanodes.展开更多
In an anode baking horizontal flue ring furnace, the temperature distribution is one of the key factors influencing the quality of baked anode and is closely correlated with the gas flow. To understand the gas flow di...In an anode baking horizontal flue ring furnace, the temperature distribution is one of the key factors influencing the quality of baked anode and is closely correlated with the gas flow. To understand the gas flow distribution in the flue, Navier Stokes equation with " k ε " two equation turbulence model was adopted and the simulation on the gas flow was performed. The numerical simulation results showed that the even direction of gas flow should be considered in the design of flue baffles and the gas flow distribution was really uneven in the flue in practical use. By adjusting the number and location of flue baffles rationally, the even distribution of gas flow can be improved obviously.展开更多
An attempt was made to build up a thick and compact oxide layer rapidly by pre-treating the Pb-Ag-Nd anode in fluoride-containing H2SO4 solution. The passivation reaction of Pb-Ag-Nd anode during pre-treatment process...An attempt was made to build up a thick and compact oxide layer rapidly by pre-treating the Pb-Ag-Nd anode in fluoride-containing H2SO4 solution. The passivation reaction of Pb-Ag-Nd anode during pre-treatment process was investigated using cyclic voltammetry, linear scanning voltammetry, environmental scanning electron microscopy and X-ray diffraction analysis. The results show that Pb F2 and PbSO4 are formed near the potential of Pb/PbSO4 couple. The pre-treatment in fluoride-containing H2SO4 solution contributes to the formation of a thick, compact and adherent passive film. Furthermore, pre-treatment in fluoride-containing H2SO4 solution also facilitates the formation of PbO2 on the anodic layer, and the reason could be attributed to the formation of more PbF2 and PbSO4 during the pre-treatment which tend to transform to PbO2 during the following electrowinning process. In addition, the anodic layer on anode with pre-treatment in fluoride-containing H2SO4 solution is thick and compact, and its predominant composition is β-PbO2. In summary, the pre-treatment in fluoride-containing H2SO4 solution benefits the formation of a desirable protective layer in a short time.展开更多
A new type of lead-based porous anode in zinc electrowinning was prepared by negative pressure infiltration. The anodic polarization potential and corrosion rate were studied and compared with those of traditional fia...A new type of lead-based porous anode in zinc electrowinning was prepared by negative pressure infiltration. The anodic polarization potential and corrosion rate were studied and compared with those of traditional fiat anodes （Pb-0.8%Ag） used in industry. The anode corrosion rate was determined by anode actual current density and microstructure. The results show that the anodic oxygen evolution potential decreases first and then increases with the decrease of pore diameter. The anodic potential decreases to the lowest value of 1.729 V at the pore diameter of 1.25-1.60 mm. The porous anode can decrease its actual current density and thus decrease the anodic corrosion rate. When the pore diameter is 1.60-2.00 mm, the anodic relative corrosion rate reaches the lowest value of 52.1%.展开更多
W-doped Li4TisO12 in the form of Li4Ti4.95W0.osO12 was firstly synthesized via solid state reaction. X-ray diffraction （XRD） and scanning electron microscope （gEM） were employed to characterize the structure and m...W-doped Li4TisO12 in the form of Li4Ti4.95W0.osO12 was firstly synthesized via solid state reaction. X-ray diffraction （XRD） and scanning electron microscope （gEM） were employed to characterize the structure and morphology of Li4Ti4.psW0.05Ol2. W-doping does not change the phase composition and particle morphology, while remarkably improves its cycling stability at high charge/discharge rate. Li4Ti4.95W0.05O12 exhibits an excellent rate capability with a reversible capacity of 131.2 mA.h/g at 10C and even 118.6 mA.h/g at 20C. The substitution of W for Ti site can enhance the electronic conductivity of Li4TisO12 via the generation of mixing Ti4＋/Ti3＋, which indicates that Li4Ti4.psW0.05O12 is promising as a high rate anode for the lithium-ion batteries.展开更多
Mg-6%Al-5%Pb(mass fraction) anodes with different contents of zinc were prepared by melting and casting.The electrochemical discharge behavior of these anodes in 3.5% NaCl solutions was investigated by galvanostatic t...Mg-6%Al-5%Pb(mass fraction) anodes with different contents of zinc were prepared by melting and casting.The electrochemical discharge behavior of these anodes in 3.5% NaCl solutions was investigated by galvanostatic test and electrochemical impedance spectroscopy(EIS).The microstructures and the corroded surfaces of these anodes were studied by scanning electron microscopy(SEM) and emission spectrum analysis(ESA).The phase structures and the corrosion products of the anodes were analyzed by X-ray diffraction(XRD).The results show that zinc promotes the grain refinement of Mg-6%Al-5%Pb anode and makes the average discharge potential of Mg-6%Al-5%Pb anode more negative during galvanostatic test.Mg-6%Al-5%Pb anode with the addition of 1%(mass fraction) zinc has the best electrochemical performance.The activation mechanism of zinc to Mg-6%Al-5%Pb anode is as follows:The hydrolyzation of dissolved Zn2+ ions reduces the pH value of the solution near the surface of the anode and accelerates the dissolution of Mg(OH)2 film;The precipitated Zn(OH)2 with similar structure as Mg(OH)2 combines with Mg(OH)2 film easily and makes it break down.展开更多
Developing high-performance lithium ion batteries(LIBs)using manganese oxides as anodes is attractive due to their high theoretical capacity and abundant resources.Herein,we report a facile synthesis of hierarchical s...Developing high-performance lithium ion batteries(LIBs)using manganese oxides as anodes is attractive due to their high theoretical capacity and abundant resources.Herein,we report a facile synthesis of hierarchical spherical MnO2 containing coherent amorphous/crystalline domained by a simple yet effective redox precipitation reaction at room temperature.Further,flower-like CoMn2O4 constructed by single-crystalline spinel nanosheets has been fabricated using MnO2 as precursor.This mild methodology avoids undesired particle aggregation and loss of active surface area in conventional hydrothermal or solid-state processes.Moreover,both MnO2 and CoMn2O4 nanosheets manifest superior lithium-ion storage properties,rendering them promising applications in LIBs and other energy-related fields.展开更多
A new anodic material of ternary Pb-0.8%Ag-(0-5.0%)Bi alloy for zinc electrowinning was obtained by doping Bi.The anodic oxygen evolution potential,corrosion rate,surface products after polarization,and microstructure...A new anodic material of ternary Pb-0.8%Ag-(0-5.0%)Bi alloy for zinc electrowinning was obtained by doping Bi.The anodic oxygen evolution potential,corrosion rate,surface products after polarization,and microstructures before and after polarization were studied and compared with those of Pb-0.8%Ag anode used in industry.The results show the anodic overpotential decreases with the increase of Bi content in the alloys.When the content of Bi is 1.0%(mass fraction),the anodic overpotential is 40-50 mV lower than that of Pb-0.8%Ag anode.While the corrosion rate decreases and then increases with the increase of Bi content.The Pb-0.8%Ag-0.1%Bi anode has the lowest corrosion rate(0.090 6 mg/(h·cm2).Doping Bi influences the structure of the anodic layer,but does not change the phase.The Pb-0.8%Ag-1.0%Bi anode layer is of a more fine-grained structure compared with Pb-0.8%Ag anode.展开更多
Potassium-ion batteries(PIBs)hold promise for large-scale energy storage,necessitating the development of high-performance anode materials.Carbons with the advantage of structural versatility,are recognized as the mos...Potassium-ion batteries(PIBs)hold promise for large-scale energy storage,necessitating the development of high-performance anode materials.Carbons with the advantage of structural versatility,are recognized as the most promising anode materials for their commercialization,however the relationship between the carbon anode structure and its electrochemical performance remains unclear.A series of pitch-based soft carbons with different structures were fabricated using carbonization temperatures in the range 600–1400℃,and their changes in carbon configuration and K-storage performance as a function of carbonization temperature were investigated.Correlations between the carbon crystal size and the low-potential plateau region capacity and between the degree of structural disorder of the carbons with their sloping region capacity were revealed.Among all samples,that obtained by carbonization at 700℃had a relatively high degree of disorder and a large interlayer spacing,and had a high reversible capacity of 329.4 mAh g^(-1) with a high initial coulombic efficiency of 72.81%,and maintained a high capacity of 144.2 mAh g^(-1) at the current rate of 5 C.These findings improve our fundamental understanding of the K-storage process in carbon anodes,and thus facilitate the advance of PIBs.展开更多
文摘The advantages of sodium-ion batteries(SIBs)for large-scale energy storage are well known.Among possible anode materials,hard carbon(HC)stands out as the most viable commercial option because of its superior performance.However,there is still disagreement regarding the sodium storage mechanism in the low-voltage plateau region of HC anodes,and the structure-performance relationship between its complex multiscale micro/nanostructure and electrochemical behavior remains unclear.This paper summarizes current research progress and the major problems in understanding HC’s microstructure and sodium storage mechanism,and the relationship between them.Findings about a universal sodium storage mechanism in HC,including predictions about micropore-capacity relationships,and the opportunities and challenges for using HC anodes in commercial SIBs are presented.
文摘Metal-organic frameworks(MOFs)are import-ant as possible energy storage materials.Nitrogen-doped iron-cobalt MOFs were synthesized by a one-pot solvo-thermal method using CoCl_(3)·6H_(2)O and FeCl_(3)·6H_(2)O dis-solved in N,N-dimethylformamide,and were converted into Fe-Co embedded in N-doped porous carbon polyhedra by pyrolysis in a nitrogen atmosphere.During pyrolysis,the or-ganic ligands transformed into N-doped porous carbon which improved their structural stability and also their electrical contact with other materials.The Fe and Co are tightly bound together because of their encapsulation by the carbon nitride and are well dispersed in the carbon matrix,and improve the material’s conductivity and stability and provide additional capacity.When used as the anode for lithium-ion batteries,the material gives an initial capacity of up to 2230.7 mAh g^(-1)and a reversible capa-city of 1146.3 mAh g^(-1)is retained after 500 cycles at a current density of 0.5 A g^(-1),making it an excellent candidate for this purpose.
文摘As an emerging electrochemical energy storage technology,potassium-ion batteries(PIBs),which are considered a“beyond Li-ion”battery system,have attracted tremendous attention due to their potential for providing a high energy density,and having abundant resource,and a low cost.However,their commercialization is hindered by the lack of practical anode materials.Among various reported anodes,conventional carbon materials,including graphite,soft carbon,and hard carbon,have emerged as promising candidates because of their abundance,low cost,high conductivity,and tunable structures.However,these materials have problems such as a low initial Coulombic efficiency,significant volume expansion,and unsatisfactory cyclability and rate performance.Various strategies to solve these have been explored,including optimizing the interlayer spacing,structural design,surface coating,constructing a multifunctional framework,and forming composites.This review provides a comprehensive overview of the recent progress in conventional carbon anodes,highlighting structural design strategies,mechanisms for improving the electrochemical performance,and underscores the critical role of these materials in promoting the practical application of PIBs.
文摘Transition metal sulfides are considered promising anode materials for sodium-ion batteries(SIBs)due to their high theoretical capacity and low synthesis cost.However,is-sues such as poor cyclic stability and rate performance,arising from volume expansion and structural degradation,remain sig-nificant challenges.We report a novel FeS_(2)/CoS_(2) heterostruc-ture embedded in a 3D carbon aerogel matrix(FeS_(2)/CoS_(2)@C)synthesized by a cross-linking and vulcanization process.The resulting core-shell structure,with bimetallic FeS_(2)/CoS_(2) nano-particles encapsulated in a conductive carbon shell,effectively reduces the adverse effects of volume changes during sodiation/desodiation cycles.The 3D porous carbon network increases both ion and electron diffusion,while preventing agglomeration of the active material and maintaining interface integrity.The FeS_(2)/CoS_(2)@C composite has an outstanding electrochemical performance,including a high specific capacity of 725 mAh g^(-1)at 0.5 A g^(-1)and an exceptional rate capability of 572 mAh g^(-1)at 10 A g^(-1).It also has remarkable cycling stability with no signific-ant capacity decay over 1000 cycles at 5 A g^(-1).
文摘Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes it attractive as an anode of Li-ion batteries.Herein,through a one-pot facile high-temperature annealing route,using SBA15 as the silicon source,and embedding tin dioxide SnO_(2)particles into carbon coated SiO_(x),the mesoporous SiO_(x)-SnO_(2)@C rod composite was prepared and tested as the anode material.The results revealed that the SnO_(2)particles were distributed uniformly in the wall,which could further improve their volume energy densities.The coated carbon plays a role in maintaining structural integrality during lithiation,and the rich mesopores structure can release the expanded volume and enhance Li-ion transfer.At 0.1 A·g^(-1),the gravimetric and volumetric capacities of the composite were as high as 1271 mAh·g^(-1)and 1573 mAh·cm^(-3),respectively.After 200 cycles,the 95%capacity could be retained compared with that upon the 2nd cycle at 0.5 A·g^(-1).And the rod morphology was well kept,except that the diameter of the rod was 3 times larger than its original size after the cell was discharged into 0.01 V.
文摘Sodium-ion batteries(SIBs)have emerged as a promising contender for next-gener-ation energy storage systems.Hard carbon is re-garded as the most promising anode for commer-cial SIB,however,the large number of defects on its surface cause irreversible electrolyte consump-tion and an uneven solid electrolyte interphase film.An advanced molecular engineering strategy to coat hard carbon with polycyclic aromatic mo-lecules is reported.Specifically,polystyrene-based carbon microspheres(CSs)were first synthesized and then coated with polycyclic aromatic mo-lecules derived from coal tar pitch by spray-drying and followed by oxidation.Compared to the traditional CVD coating meth-od,this molecular framework strategy has been shown to reduce the number of defects on the surface of CSs without sacrifi-cing internal storage sites and suppressing transport kinetics in hosting the sodium ions.Besides the lower surface defect con-centration,the synthesized hybrid carbon microspheres(HCSs)have a larger grain size and more abundant closed pores,and have a higher reversible sodium storage capacity.A HCS-P-60%electrode has a capacity of 332.3 mAh g^(-1)with an initial Cou-lombic efficiency of 88.5%.It also has a superior rate performance of 246.6 mAh g^(-1)at 2 C and a 95.2%capacity retention after 100 cycles at 0.2 C.This work offers new insights into designing high-performance hard carbon microsphere anodes,advan-cing the commercialization of sodium-ion batteries.
基金supported by the National Natural Science Foundation of China(22472023,22202037)the Jilin Province Science and Technology Development Program(20250102077JC)the Fundamental Research Funds for the Central Universities(2412024QD014,2412023QD019).
文摘Direct ethanol fuel cells(DEFCs)are a promising alternative to conventional energy sources,offering high energy density,environmental sustainability,and operational safety.Compared to methanol fuel cells,DEFCs exhibit lower toxicity and a more mature preparation process.Unlike hydrogen fuel cells,DEFCs provide superior storage and transport feasibility,as well as cost-effectiveness,significantly enhancing their commercial viability.However,the stable C-C bond in ethanol creates a high activation energy barrier,often resulting in incomplete electrooxidation.Current commercial platinum(Pt)-and palladium(Pd)-based catalysts demonstrate low C-C bond cleavage efficiency(<7.5%),severely limiting DEFC energy output and power density.Furthermore,high catalyst costs and insufficient activity impede large-scale commercialization.Recent advances in DEFC anode catalyst design have focused on optimizing material composition and elucidating catalytic mechanisms.This review systematically examines developments in ethanol electrooxidation catalysts over the past five years,highlighting strategies to improve C1 pathway selectivity and C-C bond activation.Key approaches,such as alloying,nanostructure engineering,and interfacial synergy effects,are discussed alongside their mechanistic implications.Finally,we outline current challenges and future prospects for DEFC commercialization.
文摘Biomass-derived hard carbons,usually prepared by pyrolysis,are widely considered the most promising anode materials for sodium-ion bat-teries(SIBs)due to their high capacity,low poten-tial,sustainability,cost-effectiveness,and environ-mental friendliness.The pyrolysis method affects the microstructure of the material,and ultimately its so-dium storage performance.Our previous work has shown that pyrolysis in a sealed graphite vessel im-proved the sodium storage performance of the car-bon,however the changes in its microstructure and the way this influences the sodium storage are still unclear.A series of hard carbon materials derived from corncobs(CCG-T,where T is the pyrolysis temperature)were pyrolyzed in a sealed graphite vessel at different temperatures.As the pyrolysis temperature increased from 1000 to 1400℃ small carbon domains gradually transformed into long and curved domains.At the same time,a greater number of large open pores with uniform apertures,as well as more closed pores,were formed.With the further increase of pyrolysis temperature to 1600℃,the long and curved domains became longer and straighter,and some closed pores gradually became open.CCG-1400,with abundant closed pores,had a superior SIB performance,with an initial reversible ca-pacity of 320.73 mAh g^(-1) at a current density of 30 mA g^(-1),an initial Coulomb efficiency(ICE)of 84.34%,and a capacity re-tention of 96.70%after 100 cycles.This study provides a method for the precise regulation of the microcrystalline and pore structures of hard carbon materials.
基金National Natural Science Foundation of China (52073253)。
文摘Solid-state Na metal batteries(SSNBs),known for the low cost,high safety,and high energy density,hold a significant position in the next generation of rechargeable batteries.However,the urgent challenge of poor interfacial contact in solid-state electrolytes has hindered the commercialization of SSNBs.Driven by the concept of intimate electrode-electrolyte interface design,this study employs a combination of sodium-potassium(NaK)alloy and carbon nanotubes to prepare a semi-solid NaK(NKC)anode.Unlike traditional Na anodes,the paintable paste-like NKC anode exhibits superior adhesion and interface compatibility with both current collectors and gel electrolytes,significantly enhancing the physical contact of the electrode-electrolyte interface.Additionally,the filling of SiO_(2) nanoparticles improves the wettability of NaK alloy on gel polymer electrolytes,further achieving a conformal interface contact.Consequently,the overpotential of the NKC symmetric cell is markedly lower than that of the Na symmetric cell when subjected to a long cycle of 300 hrs.The full cell coupled with Na_(3)V_(2)(PO_(4))_(2) cathodes had an initial discharge capacity of 106.8 mAh·g^(-1) with a capacity retention of 89.61%after 300 cycles,and a high discharge capacity of 88.1 mAh·g^(-1) even at a high rate of 10 C.The outstanding electrochemical performance highlights the promising application potential of the NKC electrode.
基金Project(51234009)supported by the National Natural Science Foundation of ChinaProject(2014DFA90520)supported by International Cooperation Program of Ministry of Science of ChinaProject(2013A100003)supported by the Production,Teaching and Research Program of Guangdong Province,China
文摘A process was proposed to convert and separate selenium and arsenic in copper anode slime(CAS) by low-temperature alkali fusion process.Central composite design was employed to optimize the effective parameters,in which Na OH/CAS mass ratio,fusion temperature and fusion time were selected as variables,and the conversion ratio of selenium and arsenic as responses.Second-order polynomial models of high significance and 3D response surface plots were constructed to show the relationship between the responses and the variables.Optimum area of >90% selenium conversion ratio and >90% arsenic conversion ratio was obtained by the overlaid contours at Na OH/CAS mass ratio of 0.65-0.75,fusion temperature of 803-823 K and fusion time of 20-30 min.The models are validated by experiments in the optimum area,and the results demonstrate that these models are reliable and accurate in predicting the fusion process.
基金Project(2012BAE06B05)supported by the National Science and Technology Support Program of ChinaProject(N130602004)supported by the Fundamental Research Funds for the Central Universities of China
文摘The application of microwave irradiation for pretreatment of copper anode slime with high nickel content prior to pressure sulfuric acid leaching has been proposed.The microwave-assisted pretreatment is a rapid and efficient process.Through the technology of microwave assisted pretreatment-pressure leaching of copper anode slime,copper,tellurium,selenium and nickel are almost completely recovered.Under optimal conditions,the leaching efficiencies of copper,tellurium,selenium and nickel are 97.12%,95.97%,95.37% and 93.90%,respectively.The effect of microwave radiation on the temperature of copper anode slime and leaching solution is investigated.It is suggested that the enhancement on the recoveries of copper,tellurium and selenium can be attributed to the temperature gradient which is caused by shallow microwave penetration depth and super heating occurring at the solid–liquid interface.The kinetic study shows that the pressure leaching of copper anode slime,with and without microwave assisted pretreatment,are both controlled by chemical reactions on the surfaces of particles.It is found that the activation energy calculated for microwave-assisted pretreatment-pressure leaching(49.47 kJ/mol) is lower than that for pressure leaching which is without microwave assisted pretreatment(60.57 kJ/mol).
文摘A study was carried out on kinetics of oxygen evolution on lead alloy anodes in sulphuric acidicelectrolyte. The influence of alloy elements Ca, Ag and Sn on the overpotential of oxygen evolution was investigated. All anodes had been subjected to a pre-polarization before the measurement of potential-currentcurves for oxygen evolution. The overpotential of oxygen evolution was found to be decreased when the alloyanode contained Ca and Ag, whereas it remained unchanged when the alloy anode contained Sn. For oxygenevolution on lead alloy anodes the TAFEL equation was valid. The b vulue for Ph and Ph-Ca anodes was approx. 100, for Ph-Ag, Ph-Ag-Ca anodes it was approx. 140. The a value for Ph Ca, Ph-Ag, Ph-Ag-Ca anodes decreased with the increase of Ca or/and Ag content. The a and b value was not influenced by Sn in theanodes.
文摘In an anode baking horizontal flue ring furnace, the temperature distribution is one of the key factors influencing the quality of baked anode and is closely correlated with the gas flow. To understand the gas flow distribution in the flue, Navier Stokes equation with " k ε " two equation turbulence model was adopted and the simulation on the gas flow was performed. The numerical simulation results showed that the even direction of gas flow should be considered in the design of flue baffles and the gas flow distribution was really uneven in the flue in practical use. By adjusting the number and location of flue baffles rationally, the even distribution of gas flow can be improved obviously.
基金Projects(51204208,51374240)supported by the National Natural Science Foundation of ChinaProject(2014zzts028)supported by the Fundamental Research Funds for the Central Universities of Central South University,China
文摘An attempt was made to build up a thick and compact oxide layer rapidly by pre-treating the Pb-Ag-Nd anode in fluoride-containing H2SO4 solution. The passivation reaction of Pb-Ag-Nd anode during pre-treatment process was investigated using cyclic voltammetry, linear scanning voltammetry, environmental scanning electron microscopy and X-ray diffraction analysis. The results show that Pb F2 and PbSO4 are formed near the potential of Pb/PbSO4 couple. The pre-treatment in fluoride-containing H2SO4 solution contributes to the formation of a thick, compact and adherent passive film. Furthermore, pre-treatment in fluoride-containing H2SO4 solution also facilitates the formation of PbO2 on the anodic layer, and the reason could be attributed to the formation of more PbF2 and PbSO4 during the pre-treatment which tend to transform to PbO2 during the following electrowinning process. In addition, the anodic layer on anode with pre-treatment in fluoride-containing H2SO4 solution is thick and compact, and its predominant composition is β-PbO2. In summary, the pre-treatment in fluoride-containing H2SO4 solution benefits the formation of a desirable protective layer in a short time.
基金Project(2007SK2009) supported by the Science and Technology Research Project of Hunan Province, China
文摘A new type of lead-based porous anode in zinc electrowinning was prepared by negative pressure infiltration. The anodic polarization potential and corrosion rate were studied and compared with those of traditional fiat anodes （Pb-0.8%Ag） used in industry. The anode corrosion rate was determined by anode actual current density and microstructure. The results show that the anodic oxygen evolution potential decreases first and then increases with the decrease of pore diameter. The anodic potential decreases to the lowest value of 1.729 V at the pore diameter of 1.25-1.60 mm. The porous anode can decrease its actual current density and thus decrease the anodic corrosion rate. When the pore diameter is 1.60-2.00 mm, the anodic relative corrosion rate reaches the lowest value of 52.1%.
文摘W-doped Li4TisO12 in the form of Li4Ti4.95W0.osO12 was firstly synthesized via solid state reaction. X-ray diffraction （XRD） and scanning electron microscope （gEM） were employed to characterize the structure and morphology of Li4Ti4.psW0.05Ol2. W-doping does not change the phase composition and particle morphology, while remarkably improves its cycling stability at high charge/discharge rate. Li4Ti4.95W0.05O12 exhibits an excellent rate capability with a reversible capacity of 131.2 mA.h/g at 10C and even 118.6 mA.h/g at 20C. The substitution of W for Ti site can enhance the electronic conductivity of Li4TisO12 via the generation of mixing Ti4＋/Ti3＋, which indicates that Li4Ti4.psW0.05O12 is promising as a high rate anode for the lithium-ion batteries.
基金Project(JPPT-115-168) supported by the National Key Science and Technological Program of China
文摘Mg-6%Al-5%Pb(mass fraction) anodes with different contents of zinc were prepared by melting and casting.The electrochemical discharge behavior of these anodes in 3.5% NaCl solutions was investigated by galvanostatic test and electrochemical impedance spectroscopy(EIS).The microstructures and the corroded surfaces of these anodes were studied by scanning electron microscopy(SEM) and emission spectrum analysis(ESA).The phase structures and the corrosion products of the anodes were analyzed by X-ray diffraction(XRD).The results show that zinc promotes the grain refinement of Mg-6%Al-5%Pb anode and makes the average discharge potential of Mg-6%Al-5%Pb anode more negative during galvanostatic test.Mg-6%Al-5%Pb anode with the addition of 1%(mass fraction) zinc has the best electrochemical performance.The activation mechanism of zinc to Mg-6%Al-5%Pb anode is as follows:The hydrolyzation of dissolved Zn2+ ions reduces the pH value of the solution near the surface of the anode and accelerates the dissolution of Mg(OH)2 film;The precipitated Zn(OH)2 with similar structure as Mg(OH)2 combines with Mg(OH)2 film easily and makes it break down.
基金Project(JCYJ20170817110251498)supported by the Basic Research Project of the Science and Technology Innovation Commission of Shenzhen,ChinaProject(2016TQ03C919)supported by the Guangdong Special Support for the Science and Technology Leading Young Scientist,ChinaProject(21603094)supported by the National Natural Science Foundation of China
文摘Developing high-performance lithium ion batteries(LIBs)using manganese oxides as anodes is attractive due to their high theoretical capacity and abundant resources.Herein,we report a facile synthesis of hierarchical spherical MnO2 containing coherent amorphous/crystalline domained by a simple yet effective redox precipitation reaction at room temperature.Further,flower-like CoMn2O4 constructed by single-crystalline spinel nanosheets has been fabricated using MnO2 as precursor.This mild methodology avoids undesired particle aggregation and loss of active surface area in conventional hydrothermal or solid-state processes.Moreover,both MnO2 and CoMn2O4 nanosheets manifest superior lithium-ion storage properties,rendering them promising applications in LIBs and other energy-related fields.
基金Project(2007SK2009)supported by the Science and Technology Research Project of Hunan Province,China
文摘A new anodic material of ternary Pb-0.8%Ag-(0-5.0%)Bi alloy for zinc electrowinning was obtained by doping Bi.The anodic oxygen evolution potential,corrosion rate,surface products after polarization,and microstructures before and after polarization were studied and compared with those of Pb-0.8%Ag anode used in industry.The results show the anodic overpotential decreases with the increase of Bi content in the alloys.When the content of Bi is 1.0%(mass fraction),the anodic overpotential is 40-50 mV lower than that of Pb-0.8%Ag anode.While the corrosion rate decreases and then increases with the increase of Bi content.The Pb-0.8%Ag-0.1%Bi anode has the lowest corrosion rate(0.090 6 mg/(h·cm2).Doping Bi influences the structure of the anodic layer,but does not change the phase.The Pb-0.8%Ag-1.0%Bi anode layer is of a more fine-grained structure compared with Pb-0.8%Ag anode.
文摘Potassium-ion batteries(PIBs)hold promise for large-scale energy storage,necessitating the development of high-performance anode materials.Carbons with the advantage of structural versatility,are recognized as the most promising anode materials for their commercialization,however the relationship between the carbon anode structure and its electrochemical performance remains unclear.A series of pitch-based soft carbons with different structures were fabricated using carbonization temperatures in the range 600–1400℃,and their changes in carbon configuration and K-storage performance as a function of carbonization temperature were investigated.Correlations between the carbon crystal size and the low-potential plateau region capacity and between the degree of structural disorder of the carbons with their sloping region capacity were revealed.Among all samples,that obtained by carbonization at 700℃had a relatively high degree of disorder and a large interlayer spacing,and had a high reversible capacity of 329.4 mAh g^(-1) with a high initial coulombic efficiency of 72.81%,and maintained a high capacity of 144.2 mAh g^(-1) at the current rate of 5 C.These findings improve our fundamental understanding of the K-storage process in carbon anodes,and thus facilitate the advance of PIBs.
