Under steady-state conditions, the general currents of EE reactions at disk,hemispherical and spherical microelectrodes are derived.From these equations, some electrode reaction parameters can be very simply obtained.
The development of shape-customizable and bulk flexible electrochemical devices through processing technologies as versatile as those used for plastics promises to revolutionize the future of battery technology.Howeve...The development of shape-customizable and bulk flexible electrochemical devices through processing technologies as versatile as those used for plastics promises to revolutionize the future of battery technology.However,this pursuit has been fundamentally hindered by the absence of transformative battery materials capable of delivering the necessary electrochemical functions,robust interface adhesion,and,crucially,the suitable rheological properties required for on-demand shaping.In this work,we introduce a concept of a multifunctional plasticine electrode matrix(PEM)featuring nano-interpenetrating networks(nano-IPN)to address this challenge.Utilizing the nonflammable liquid-electrolyte hydration combined with conductive nanomaterials,we have realized a PEM in the form of a multifunctional nanocomposite that integrates ion and electron conduction,component binding,non-flammability,and plasticine-like moldability.With this PEM,we have successfully fabricated a variety of bulk-flexible electrodes with high mass loading of active material(AM)(>70 wt%)using industry-friendly extrusion and compression molding techniques.Moreover,these high AM-loading composite electrodes achieve an unparalleled bulk conformability and flexibility,remaining structurally intact even under severe mechanical stress.Ultimately,we have successfully produced shape-patternable and flexible batteries via extrusion molding.This study underscores the potential of the PEM to revolutionize battery microstructures,interfaces,manufacturing processes,and performance characteristics.展开更多
The development of low-energy consumption and environmentally friendly electrodeposition of metal/alloy films or coatings is presently one of the primary topics for the research community.For this purpose,deep eutecti...The development of low-energy consumption and environmentally friendly electrodeposition of metal/alloy films or coatings is presently one of the primary topics for the research community.For this purpose,deep eutectic solvents(DESs)are valued as electrolytes for their advantages of low operating temperature and wide electrochemical windows.At present,there is large amount of literature on this emerging field,but there are no specialized reviews of these studies.Here,after a brief introduction of DESs’concept and history,we comprehensively reviewed the lastest progress on the metal/alloy electrodeposition in DESs.Additionally,we discussed the key influence factors of the electrodeposition process and analyzed the corresponding mechanisms.Based on these,we emphasized the importance of the establishment of predictive models for dealing with the challenges in large-scale applications.展开更多
Metal coating is a prevalent strategy for enhancing surface properties.Among the numerous methods for preparing coatings,electrodeposition stands out due to its simplicity,cost-effectiveness,and high efficiency,making...Metal coating is a prevalent strategy for enhancing surface properties.Among the numerous methods for preparing coatings,electrodeposition stands out due to its simplicity,cost-effectiveness,and high efficiency,making it widely utilized in various metal coating applications.By meticulously selecting appropriate electrolytes and electrodeposition parameters,metal coatings with diverse structures and morphologies can be obtained,and tailored to meet specific performance requirements.As the demand for superior metal coating performance continues to rise,it is imperative to summarize and forecast electrodeposition techniques to meet the criteria for high quality and precision.This review delves into the electrodeposition preparation of several typical metal coatings in diverse electrolyte systems,including aqueous solutions,ionic liquids,deep eutectic solvents,and molten salts.We also examine the electrodeposition process on the cathode,elucidate the correlation between parameters and coating quality,and suggest future research directions.This review aims to provide valuable insights and guidance for the electrodeposition preparation of metal coatings.展开更多
Supercapacitors are efficient and versatile energy storage devices,offering remarkable power density,fast charge/discharge rates,and exceptional cycle life.As research continues to push the boundaries of their perform...Supercapacitors are efficient and versatile energy storage devices,offering remarkable power density,fast charge/discharge rates,and exceptional cycle life.As research continues to push the boundaries of their performance,electrode fabrication techniques are critical aspects influencing the overall capabilities of supercapacitors.Herein,we aim to shed light on the advantages offered by dry electrode processing for advanced supercapacitors.Notably,our study explores the performance of these electrodes in three different types of electrolytes:organic,ionic liquids,and quasi-solid states.By examining the impact of dry electrode processing on various electrode and electrolyte systems,we show valuable insights into the versatility and efficacy of this technique.The supercapacitors employing dry electrodes demonstrated significant improvements compared with conventional wet electrodes,with a lifespan extension of+45%in organic,+192%in ionic liquids,and+84%in quasi-solid electrolytes.Moreover,the increased electrode densities achievable through the dry approach directly translate to improved volumetric outputs,enhancing energy storage capacities within compact form factors.Notably,dry electrode-prepared supercapacitors outperformed their wet electrode counterparts,exhibiting a higher energy density of 6.1 Wh cm^(-3)compared with 4.7 Wh cm^(-3)at a high power density of 195Wcm^(-3),marking a substantial 28%energy improvement in the quasi-solid electrolyte.展开更多
The kinetics of the deposition of lithium on aluminium electrode has been studied by cyclic voltammetry.The deposition of lithium on aluminium electrode was found to be controlled by the diffusion of lithium within t...The kinetics of the deposition of lithium on aluminium electrode has been studied by cyclic voltammetry.The deposition of lithium on aluminium electrode was found to be controlled by the diffusion of lithium within the β-LiAl alloy probably through the vacancy mechanism. The limiting operating potential and current for prepanng the lithium aluminium electrodes were given.展开更多
The electrode process of pyrite in diethyldithiocarbamate (DDTC) solution pH 11.4 was investigated by using cyclic voltammetry, potentiost atic and chronopotentiometry. Tetraethylthioram disulphide(TETD) was electrode...The electrode process of pyrite in diethyldithiocarbamate (DDTC) solution pH 11.4 was investigated by using cyclic voltammetry, potentiost atic and chronopotentiometry. Tetraethylthioram disulphide(TETD) was electrodepo sited on pyrite electrode surface as the electrode potential is higher than 0.2 V. The relationship of the current density caused by diffusion and reaction time can be ascertained as i =1/(9.08×10 -5 +4.77×10 -3 t 0.5 ) , and the diffusion coefficient of DDTC on pyrite surface is about 3.72×10 - 6 cm 2/s. At pH 11.4, the thickness of TETD adsorbed on pyr ite surface is about 1.63 molecule layer. The electrochemical dynamics equation of the reduction of TETD on pyrite surface is given as η =0.116-0.064log[1- ( t/τ ) 0.5 ]. The kinetic parameters were determined as follows: the ex change current density ( i 0) is 3.08 μA/cm 2; the transmission coeffi cient( α ) is 0.462.展开更多
In this study,the characteristics and solidification behavior of Ti-48Al-3Nb-1.5Ta powder produced by supreme-speed plasma rotating electrode process(SS-PREP®)were investigated.The microstructure,phase and charac...In this study,the characteristics and solidification behavior of Ti-48Al-3Nb-1.5Ta powder produced by supreme-speed plasma rotating electrode process(SS-PREP®)were investigated.The microstructure,phase and characteristics were analyzed by scanning electron microscopy,X-ray diffraction and other methods.The atomization mechanism is direct drop formation.The relationship between the particle size and cooling rate is vc=3.14×10^(-7)·d^(-2)+1.18×10^(-2)·d^(3/2),and the relationship between secondary dendrite arm space and the particle size isλ=0.028d+0.11,as well as the relationship between SDAS and cooling rate isλ=4.84×10^(-5)·T^(-1.43).With increase in particle size,the surface structure gradually changes from the featureless smooth structure to dendritic and cellular dendritic morphology,and the flow ability becomes better.The carbides mainly exist within 5 nm of the surface and the oxidation layer is about 20 nm thick.Ti-48Al-3Nb-1.5Ta powder was mainly composed ofα2 phase andγphase.With increase in particle size,the content ofγphase increases,and the hardness decreases accordingly.The 106–250μm particles are composed of multiple grains with the grain size of 70–80μm.The microstructure,phase composition and hardness of different TiAl powders with the same size are similar,but the elastic modulus is different.展开更多
The electrochemical behaviour of Ti(Ⅲ) and Ti(Ⅱ) in LiCl-KCl eutectic system has been studied by cyclic voltammetry and chronoamperometry.The cathodic reduction of Ti(Ⅲ) and Ti(Ⅱ) has been found to be stepwise:Ti(...The electrochemical behaviour of Ti(Ⅲ) and Ti(Ⅱ) in LiCl-KCl eutectic system has been studied by cyclic voltammetry and chronoamperometry.The cathodic reduction of Ti(Ⅲ) and Ti(Ⅱ) has been found to be stepwise:Ti(Ⅲ)+e=Ti(Ⅱ),Ti(Ⅱ)+2e =Ti.The reductions are diffusion controlled.When an equilibrium between Ti subchlorides and excess metallic Ti was estab- lished by reaction 2TiCl_3+Ti=3TiCl_2 in LiCl-KCl melt at 475℃,then the average valence of Ti is less than 2.1.In this system the diffusion coefficient for Ti(Ⅱ) ion was calculated as D=2.5×10^(-5)cm^2·s^(-1).The chronoamperometric studies showed that the initial nucleation stage and growth of nuclei were observed when Ti ions were electrodeposited on low carbon steel substrate. The investigation of nucleation of metal may provide the method for obtaining smooth,coherent and adherent deposits of titanium.展开更多
The electrode process of diethyldithiocarbamate on the surface of pyrrhotite was studied using systematic electrochemical analysis, including cyclic voltammetry, chronopotentiometry and galvanostatic. Experimental res...The electrode process of diethyldithiocarbamate on the surface of pyrrhotite was studied using systematic electrochemical analysis, including cyclic voltammetry, chronopotentiometry and galvanostatic. Experimental results show that tetraethylthioram disulphide（TETD） is electrodeposited on pyrrhotite electrode surface in the presence of 1.0×10^-4 mol/L diethyldithiocarbamate when the electrode potential is higher than 0.25 V. The electrochemical kinetics parameters of the electrode process of diethyldithiocarbamate on surface of pyrrhotite are calculated as follows： the exchange current density is 2.48μA/cm^2 , and the transmission coefficient is 0.46. The electrodeposition includes two steps electrochemical reaction. The first reaction is electrochemical adsorption of diethyldithiocarbamatc ion, then the adsorbed ion associates with a diethyldithiocarbamate ion from the solution and forms tetraethylthioram disulphide on the surface of pyrrhotite.展开更多
TiO2 nanotube （TINT） electrodes anodized in fluorinated organic solutions were successfully prepared on Ti sheets. Field-emission scanning electron microscopy （FE-SEM） and X-ray diffraction （XRD） were performed ...TiO2 nanotube （TINT） electrodes anodized in fluorinated organic solutions were successfully prepared on Ti sheets. Field-emission scanning electron microscopy （FE-SEM） and X-ray diffraction （XRD） were performed to characterize the TiNT electrodes. The linear voltammetry results under irradiation showed that the TiNT electrode annealed at 450℃ presented the highest photoelectrochemical activity. By combining photocatalytic with electrochemical process, a significantly synergetic effect on ammonia degradation was observed with Na2SO4 as supporting electrolyte at pH 10.7. Furthermore, the photoelectrocatalytic efficiency on the ammonia degradation was greatly enhanced in presence of chloride ions without the limitation ofpH. The degradation rate was improved by 14.8 times reaching 4.98 × 10^-2 min^-1 at pH 10.7 and a faster degradation rate of 6.34 × 10^-2 min^-1 was obtained at pH 3.01. The in situ photoelectrocatalytic generated active chlorine was proposed to be responsible for the improved efficiency. On the other hand, an enhanced degradation of ammonia using TiNT electrode fabricated in fluorinated organic solution was also confirmed compared to TiNT electrode anodized in fluorinated water solution and TiO2 film electrode fabricated by sol-gel method. Finally, the effect of chloride concentration was also discussed.展开更多
Fabrication of stable,reproducible and reusable reference electrodes for low energy and high-temperature steam splitting is of great interest for hydrogen fuel production without anthropogenic carbon dioxide(CO2)emiss...Fabrication of stable,reproducible and reusable reference electrodes for low energy and high-temperature steam splitting is of great interest for hydrogen fuel production without anthropogenic carbon dioxide(CO2)emission.This study has been conducted for the detection of suitable material for the fabrication of novel reference electrode.In the present scenario,this research is designed to fabricate a novel nickel reference electrode by using operating conditions of eutectic molten hydroxide(NaOH-KOH,49-51 mol%)at temperature 300℃in an ion-conducting membrane of alumina and mullite tube.Afterwards,the designed nickel reference electrode has been examined for its reusability and stability by using electrochemical technique and cyclic voltammetry.Five scans of cyclic voltammetry are performed for both membrane fabricated reference electrode.A slight positive shift in oxidation peaks is observed for mullite membrane electrode(64 mV from scan 1 to 5).The stability measurements are noted by changing the scan rate between 50 and 150 mV s−1.Furthermore,the results show that the Ni/Ni(OH)2 reference electrode covered with a mullite membrane is stable and reusable at 300℃temperature without any deterioration.The stability and reusability of prepared nickel reference electrode covered by mullite tube in the eutectic molten hydroxide were up to 9 days to carry out an electrochemical investigation,while for alumina tube reference electrode the stability and reliability were up to 3 days.The internal electrolytic material and ionic conductance can play an important role for future studies with this reference electrode along with optimisation of temperature and scan rate parameters.展开更多
The electrode process of Y^(3+)ion on molybdenum and nickel electrodes has been studied by cyclic voltammetry and chronopotentiometry in the YCl_3-NaCl-KCl melt.The overall charge transfer process is a two-step reacti...The electrode process of Y^(3+)ion on molybdenum and nickel electrodes has been studied by cyclic voltammetry and chronopotentiometry in the YCl_3-NaCl-KCl melt.The overall charge transfer process is a two-step reaction:Y^(3+)+e=Y^(2+);Y^(2+)+2e=Y.Yttrium reduced on the nickel electrode can form a series of Ni-Y alloys.X-ray diffraction analysis was employed to determine the alloy compositions formed under different con- ditions.展开更多
The reduction of yttrium ion on copper electrode in NaCl-KCl-YCl3 molten salts has been investigated.The results indicate that several humps for formation of intermetallic compounds occur before metallic yttrium is pr...The reduction of yttrium ion on copper electrode in NaCl-KCl-YCl3 molten salts has been investigated.The results indicate that several humps for formation of intermetallic compounds occur before metallic yttrium is produced. The formation of intermetallic compounds is controlled by diffusion of yttrium into copper electrode. The application of theoretical results to diffusion of yttrium atoms into copper substrate is discussed also.展开更多
In this study, the electrochemical reduction of Y(Ⅲ)on nickel electrode has been investigated. The resultsshow that there are several plateaus for formation of intermetallic compounds preceding reduction peak ofyttri...In this study, the electrochemical reduction of Y(Ⅲ)on nickel electrode has been investigated. The resultsshow that there are several plateaus for formation of intermetallic compounds preceding reduction peak ofyttrium. A linear relationship between the current and t￣(-1/2) has been obtained, showing that Cottrell's law isobeyed.展开更多
The electrode process of galena in diethyldithiocarbamate (DDTC) solution at pH 11.4 has been investigated using cyclic voltammetry, potentiostatic and chronopotentiometry. Electrodeposit of PbD 2 on galena electrode ...The electrode process of galena in diethyldithiocarbamate (DDTC) solution at pH 11.4 has been investigated using cyclic voltammetry, potentiostatic and chronopotentiometry. Electrodeposit of PbD 2 on galena electrode surface can occur while the electrode potential is higher than -0.05?V. The relationship between the current density caused by diffusion and reaction time has been ascertained, and the diffusion coefficient of DDTC on galena surface in DDTC solution is about 1.12×10 -6 cm 2/s. A passive PbD 2 film covers the surface of galena electrode.展开更多
The surface microstructure and the surface segregation of FGH 95 nickel-basedsuperalloy powders prepared through plasma rotating electrode processing (PREP) have beeninvestigated by using SEM and AES. The results indi...The surface microstructure and the surface segregation of FGH 95 nickel-basedsuperalloy powders prepared through plasma rotating electrode processing (PREP) have beeninvestigated by using SEM and AES. The results indicate that the surface microstructure of powderschanges from dendrite into cellular stricture as the particle size of powders decrease, and thepredominant precipitates solidified on the particle surfaces were identified as MC' type carbidesenriched with Nb and Ti. It was also indicated that along with the depth of particle surfaces, thesegregation layer of S, C and O elements are thick, and that of Ti, Cr elements are thin for largesire powders while they are in reverse for median size particles.展开更多
In order to investigate the influence of processing parameters on the granularity distribution of superalloy powders during the atomization of plasma rotating electrode processing (PREP), in this paper FGH95 superallo...In order to investigate the influence of processing parameters on the granularity distribution of superalloy powders during the atomization of plasma rotating electrode processing (PREP), in this paper FGH95 superalloy powders is prepared under different processing conditions by PREP and the influence of PREP processing parameters on the granularity distribution of FGH95 superalloy powders is discussed based on fractal geometry theory. The results show that with the increase of rotating velocity of the self-consuming electrode, the fractal dimension of the granularity distribution increases linearly, which results in the increase of the proportion of smaller powders. The change of interval between plasma gun and the self-consuming electrode has a little effect on the granularity distribution, also the fractal dimension of the granularity distribution changed a little correspondingly.展开更多
Al-Cu-Y alloys were prepared by molten salt electrolysis in fluoride-oxide system composed of electrolyte（Na3 AlF6-AlF3-LiF-MgF2） and oxide（Al2 O3-CuO-Y2 O3）. Cathodic reduction process of Al2 O3,CuO and Y2 O3 wer...Al-Cu-Y alloys were prepared by molten salt electrolysis in fluoride-oxide system composed of electrolyte（Na3 AlF6-AlF3-LiF-MgF2） and oxide（Al2 O3-CuO-Y2 O3）. Cathodic reduction process of Al2 O3,CuO and Y2 O3 were analyzed by cyclic voltammetry and chronoamperometry. Components and phase composition of alloy samples prepared by potentiostatic electrolysis were characterized by scanning electron microscopy and energy dispersive spectroscopy. The results show that the Al-Cu-Y alloy can be prepared in the AIF3-NaF-5 wt%LiF-5 wt%MgF2（NaF/AlF3 = 2.2, molecular ratio） eutectic system with mixed oxide（Al2 O3-CuO-Y2 O3） through 2 h at the conditions of a temperature of 1208 K, cell voltage3.0 V, cathode current density 0.7 A/cm^2. Al（Ⅲ） and Cu（Ⅱ） ions can be reduced to zero valence Al（0） and Cu（0） directly on carbonaceous electrode surface by instantaneous nucleation, respectively, the reduction process is controlled by diffusion. The reduction potential of Y（Ⅲ） ions is close to the active ions of fluoride melts, but strengthened phase AI3 Y can be formed through electrochemical reduction and alloyed process with active Al（Ⅲ） and Cu（Ⅱ） ions, meanwhile, the Al2 Cu and Al3 Y phases are distributed at the grain boundary of Al matrix.展开更多
The electrode kinetics of cerium on aluminium electrode and its effects on the behavior of the lithium-aluminium anode were studied by using cyclic voltammetry and chronoamperometry. The electrochemical properties and...The electrode kinetics of cerium on aluminium electrode and its effects on the behavior of the lithium-aluminium anode were studied by using cyclic voltammetry and chronoamperometry. The electrochemical properties and physical behavior of lithium-aluminium anode were improved by adding cerium into aluminium before lithium was deposited. Some parameters for preparing lithium-aluminium electrodes were also given.展开更多
文摘Under steady-state conditions, the general currents of EE reactions at disk,hemispherical and spherical microelectrodes are derived.From these equations, some electrode reaction parameters can be very simply obtained.
基金financial support from the National Natural Science Foundation of China(52473248,52203123,52125301,22279070 and U21A20170)the State Key Laboratory of Polymer Materials Engineering(Grant No:sklpme 2023-1-05 and sklpme 2024-2-04)+3 种基金the Ministry of Science and Technology of China(No.2019YFA0705703)the Sichuan Science and Technology Program(2023NSFSC0991 and 2025ZNSFSC1411)the Fundamental Research Funds for the Central Universitiespartially sponsored by the Double First-Class Construction Funds of Sichuan University.
文摘The development of shape-customizable and bulk flexible electrochemical devices through processing technologies as versatile as those used for plastics promises to revolutionize the future of battery technology.However,this pursuit has been fundamentally hindered by the absence of transformative battery materials capable of delivering the necessary electrochemical functions,robust interface adhesion,and,crucially,the suitable rheological properties required for on-demand shaping.In this work,we introduce a concept of a multifunctional plasticine electrode matrix(PEM)featuring nano-interpenetrating networks(nano-IPN)to address this challenge.Utilizing the nonflammable liquid-electrolyte hydration combined with conductive nanomaterials,we have realized a PEM in the form of a multifunctional nanocomposite that integrates ion and electron conduction,component binding,non-flammability,and plasticine-like moldability.With this PEM,we have successfully fabricated a variety of bulk-flexible electrodes with high mass loading of active material(AM)(>70 wt%)using industry-friendly extrusion and compression molding techniques.Moreover,these high AM-loading composite electrodes achieve an unparalleled bulk conformability and flexibility,remaining structurally intact even under severe mechanical stress.Ultimately,we have successfully produced shape-patternable and flexible batteries via extrusion molding.This study underscores the potential of the PEM to revolutionize battery microstructures,interfaces,manufacturing processes,and performance characteristics.
基金financially supported from the National Natural Science Foundation of China(Nos.52274291,52204305)Beijing Institute of Technology Research Fund Program for Young Scholars,China(No.1740011182102).
文摘The development of low-energy consumption and environmentally friendly electrodeposition of metal/alloy films or coatings is presently one of the primary topics for the research community.For this purpose,deep eutectic solvents(DESs)are valued as electrolytes for their advantages of low operating temperature and wide electrochemical windows.At present,there is large amount of literature on this emerging field,but there are no specialized reviews of these studies.Here,after a brief introduction of DESs’concept and history,we comprehensively reviewed the lastest progress on the metal/alloy electrodeposition in DESs.Additionally,we discussed the key influence factors of the electrodeposition process and analyzed the corresponding mechanisms.Based on these,we emphasized the importance of the establishment of predictive models for dealing with the challenges in large-scale applications.
基金financial support from the Project supported by the Southern Marine Science and Engineering Guangdong Lab-oratory(Zhuhai)(No.SML2023SP242)the National Natural Sci-ence Foundation of China(Nos.52274291 and 52204305)the Beijing Institute of Technology Research Fund Program for Young Scholars(No.1740011182102).
文摘Metal coating is a prevalent strategy for enhancing surface properties.Among the numerous methods for preparing coatings,electrodeposition stands out due to its simplicity,cost-effectiveness,and high efficiency,making it widely utilized in various metal coating applications.By meticulously selecting appropriate electrolytes and electrodeposition parameters,metal coatings with diverse structures and morphologies can be obtained,and tailored to meet specific performance requirements.As the demand for superior metal coating performance continues to rise,it is imperative to summarize and forecast electrodeposition techniques to meet the criteria for high quality and precision.This review delves into the electrodeposition preparation of several typical metal coatings in diverse electrolyte systems,including aqueous solutions,ionic liquids,deep eutectic solvents,and molten salts.We also examine the electrodeposition process on the cathode,elucidate the correlation between parameters and coating quality,and suggest future research directions.This review aims to provide valuable insights and guidance for the electrodeposition preparation of metal coatings.
基金funding of the joint Polish-German project SUPILMIX(PR-1173/27)by the German Research Foundation(DFG,Deutsche Forschungsgemeinschaft)+1 种基金funding from the Alexander von Humboldt Foundation.D.L.the German Chemical Industry Fund for the financial support through a Liebig Fellowship.
文摘Supercapacitors are efficient and versatile energy storage devices,offering remarkable power density,fast charge/discharge rates,and exceptional cycle life.As research continues to push the boundaries of their performance,electrode fabrication techniques are critical aspects influencing the overall capabilities of supercapacitors.Herein,we aim to shed light on the advantages offered by dry electrode processing for advanced supercapacitors.Notably,our study explores the performance of these electrodes in three different types of electrolytes:organic,ionic liquids,and quasi-solid states.By examining the impact of dry electrode processing on various electrode and electrolyte systems,we show valuable insights into the versatility and efficacy of this technique.The supercapacitors employing dry electrodes demonstrated significant improvements compared with conventional wet electrodes,with a lifespan extension of+45%in organic,+192%in ionic liquids,and+84%in quasi-solid electrolytes.Moreover,the increased electrode densities achievable through the dry approach directly translate to improved volumetric outputs,enhancing energy storage capacities within compact form factors.Notably,dry electrode-prepared supercapacitors outperformed their wet electrode counterparts,exhibiting a higher energy density of 6.1 Wh cm^(-3)compared with 4.7 Wh cm^(-3)at a high power density of 195Wcm^(-3),marking a substantial 28%energy improvement in the quasi-solid electrolyte.
文摘The kinetics of the deposition of lithium on aluminium electrode has been studied by cyclic voltammetry.The deposition of lithium on aluminium electrode was found to be controlled by the diffusion of lithium within the β-LiAl alloy probably through the vacancy mechanism. The limiting operating potential and current for prepanng the lithium aluminium electrodes were given.
文摘The electrode process of pyrite in diethyldithiocarbamate (DDTC) solution pH 11.4 was investigated by using cyclic voltammetry, potentiost atic and chronopotentiometry. Tetraethylthioram disulphide(TETD) was electrodepo sited on pyrite electrode surface as the electrode potential is higher than 0.2 V. The relationship of the current density caused by diffusion and reaction time can be ascertained as i =1/(9.08×10 -5 +4.77×10 -3 t 0.5 ) , and the diffusion coefficient of DDTC on pyrite surface is about 3.72×10 - 6 cm 2/s. At pH 11.4, the thickness of TETD adsorbed on pyr ite surface is about 1.63 molecule layer. The electrochemical dynamics equation of the reduction of TETD on pyrite surface is given as η =0.116-0.064log[1- ( t/τ ) 0.5 ]. The kinetic parameters were determined as follows: the ex change current density ( i 0) is 3.08 μA/cm 2; the transmission coeffi cient( α ) is 0.462.
基金financially supported by the Key R&D Program of Shaanxi(Program No.2022GY-388).
文摘In this study,the characteristics and solidification behavior of Ti-48Al-3Nb-1.5Ta powder produced by supreme-speed plasma rotating electrode process(SS-PREP®)were investigated.The microstructure,phase and characteristics were analyzed by scanning electron microscopy,X-ray diffraction and other methods.The atomization mechanism is direct drop formation.The relationship between the particle size and cooling rate is vc=3.14×10^(-7)·d^(-2)+1.18×10^(-2)·d^(3/2),and the relationship between secondary dendrite arm space and the particle size isλ=0.028d+0.11,as well as the relationship between SDAS and cooling rate isλ=4.84×10^(-5)·T^(-1.43).With increase in particle size,the surface structure gradually changes from the featureless smooth structure to dendritic and cellular dendritic morphology,and the flow ability becomes better.The carbides mainly exist within 5 nm of the surface and the oxidation layer is about 20 nm thick.Ti-48Al-3Nb-1.5Ta powder was mainly composed ofα2 phase andγphase.With increase in particle size,the content ofγphase increases,and the hardness decreases accordingly.The 106–250μm particles are composed of multiple grains with the grain size of 70–80μm.The microstructure,phase composition and hardness of different TiAl powders with the same size are similar,but the elastic modulus is different.
文摘The electrochemical behaviour of Ti(Ⅲ) and Ti(Ⅱ) in LiCl-KCl eutectic system has been studied by cyclic voltammetry and chronoamperometry.The cathodic reduction of Ti(Ⅲ) and Ti(Ⅱ) has been found to be stepwise:Ti(Ⅲ)+e=Ti(Ⅱ),Ti(Ⅱ)+2e =Ti.The reductions are diffusion controlled.When an equilibrium between Ti subchlorides and excess metallic Ti was estab- lished by reaction 2TiCl_3+Ti=3TiCl_2 in LiCl-KCl melt at 475℃,then the average valence of Ti is less than 2.1.In this system the diffusion coefficient for Ti(Ⅱ) ion was calculated as D=2.5×10^(-5)cm^2·s^(-1).The chronoamperometric studies showed that the initial nucleation stage and growth of nuclei were observed when Ti ions were electrodeposited on low carbon steel substrate. The investigation of nucleation of metal may provide the method for obtaining smooth,coherent and adherent deposits of titanium.
文摘The electrode process of diethyldithiocarbamate on the surface of pyrrhotite was studied using systematic electrochemical analysis, including cyclic voltammetry, chronopotentiometry and galvanostatic. Experimental results show that tetraethylthioram disulphide（TETD） is electrodeposited on pyrrhotite electrode surface in the presence of 1.0×10^-4 mol/L diethyldithiocarbamate when the electrode potential is higher than 0.25 V. The electrochemical kinetics parameters of the electrode process of diethyldithiocarbamate on surface of pyrrhotite are calculated as follows： the exchange current density is 2.48μA/cm^2 , and the transmission coefficient is 0.46. The electrodeposition includes two steps electrochemical reaction. The first reaction is electrochemical adsorption of diethyldithiocarbamatc ion, then the adsorbed ion associates with a diethyldithiocarbamate ion from the solution and forms tetraethylthioram disulphide on the surface of pyrrhotite.
基金supported by the National Natural Science Foundation of China (Nos. 21277134, 21107103)the State Key Laboratory of Environmental, Criteria and Risk Assessment Chinese Research Academy of Environmental Sciences
文摘TiO2 nanotube （TINT） electrodes anodized in fluorinated organic solutions were successfully prepared on Ti sheets. Field-emission scanning electron microscopy （FE-SEM） and X-ray diffraction （XRD） were performed to characterize the TiNT electrodes. The linear voltammetry results under irradiation showed that the TiNT electrode annealed at 450℃ presented the highest photoelectrochemical activity. By combining photocatalytic with electrochemical process, a significantly synergetic effect on ammonia degradation was observed with Na2SO4 as supporting electrolyte at pH 10.7. Furthermore, the photoelectrocatalytic efficiency on the ammonia degradation was greatly enhanced in presence of chloride ions without the limitation ofpH. The degradation rate was improved by 14.8 times reaching 4.98 × 10^-2 min^-1 at pH 10.7 and a faster degradation rate of 6.34 × 10^-2 min^-1 was obtained at pH 3.01. The in situ photoelectrocatalytic generated active chlorine was proposed to be responsible for the improved efficiency. On the other hand, an enhanced degradation of ammonia using TiNT electrode fabricated in fluorinated organic solution was also confirmed compared to TiNT electrode anodized in fluorinated water solution and TiO2 film electrode fabricated by sol-gel method. Finally, the effect of chloride concentration was also discussed.
文摘Fabrication of stable,reproducible and reusable reference electrodes for low energy and high-temperature steam splitting is of great interest for hydrogen fuel production without anthropogenic carbon dioxide(CO2)emission.This study has been conducted for the detection of suitable material for the fabrication of novel reference electrode.In the present scenario,this research is designed to fabricate a novel nickel reference electrode by using operating conditions of eutectic molten hydroxide(NaOH-KOH,49-51 mol%)at temperature 300℃in an ion-conducting membrane of alumina and mullite tube.Afterwards,the designed nickel reference electrode has been examined for its reusability and stability by using electrochemical technique and cyclic voltammetry.Five scans of cyclic voltammetry are performed for both membrane fabricated reference electrode.A slight positive shift in oxidation peaks is observed for mullite membrane electrode(64 mV from scan 1 to 5).The stability measurements are noted by changing the scan rate between 50 and 150 mV s−1.Furthermore,the results show that the Ni/Ni(OH)2 reference electrode covered with a mullite membrane is stable and reusable at 300℃temperature without any deterioration.The stability and reusability of prepared nickel reference electrode covered by mullite tube in the eutectic molten hydroxide were up to 9 days to carry out an electrochemical investigation,while for alumina tube reference electrode the stability and reliability were up to 3 days.The internal electrolytic material and ionic conductance can play an important role for future studies with this reference electrode along with optimisation of temperature and scan rate parameters.
文摘The electrode process of Y^(3+)ion on molybdenum and nickel electrodes has been studied by cyclic voltammetry and chronopotentiometry in the YCl_3-NaCl-KCl melt.The overall charge transfer process is a two-step reaction:Y^(3+)+e=Y^(2+);Y^(2+)+2e=Y.Yttrium reduced on the nickel electrode can form a series of Ni-Y alloys.X-ray diffraction analysis was employed to determine the alloy compositions formed under different con- ditions.
文摘The reduction of yttrium ion on copper electrode in NaCl-KCl-YCl3 molten salts has been investigated.The results indicate that several humps for formation of intermetallic compounds occur before metallic yttrium is produced. The formation of intermetallic compounds is controlled by diffusion of yttrium into copper electrode. The application of theoretical results to diffusion of yttrium atoms into copper substrate is discussed also.
文摘In this study, the electrochemical reduction of Y(Ⅲ)on nickel electrode has been investigated. The resultsshow that there are several plateaus for formation of intermetallic compounds preceding reduction peak ofyttrium. A linear relationship between the current and t￣(-1/2) has been obtained, showing that Cottrell's law isobeyed.
文摘The electrode process of galena in diethyldithiocarbamate (DDTC) solution at pH 11.4 has been investigated using cyclic voltammetry, potentiostatic and chronopotentiometry. Electrodeposit of PbD 2 on galena electrode surface can occur while the electrode potential is higher than -0.05?V. The relationship between the current density caused by diffusion and reaction time has been ascertained, and the diffusion coefficient of DDTC on galena surface in DDTC solution is about 1.12×10 -6 cm 2/s. A passive PbD 2 film covers the surface of galena electrode.
基金This work is financially supported by The National Defence Committee of ChineseTechnology(No.95-YJ-20)
文摘The surface microstructure and the surface segregation of FGH 95 nickel-basedsuperalloy powders prepared through plasma rotating electrode processing (PREP) have beeninvestigated by using SEM and AES. The results indicate that the surface microstructure of powderschanges from dendrite into cellular stricture as the particle size of powders decrease, and thepredominant precipitates solidified on the particle surfaces were identified as MC' type carbidesenriched with Nb and Ti. It was also indicated that along with the depth of particle surfaces, thesegregation layer of S, C and O elements are thick, and that of Ti, Cr elements are thin for largesire powders while they are in reverse for median size particles.
文摘In order to investigate the influence of processing parameters on the granularity distribution of superalloy powders during the atomization of plasma rotating electrode processing (PREP), in this paper FGH95 superalloy powders is prepared under different processing conditions by PREP and the influence of PREP processing parameters on the granularity distribution of FGH95 superalloy powders is discussed based on fractal geometry theory. The results show that with the increase of rotating velocity of the self-consuming electrode, the fractal dimension of the granularity distribution increases linearly, which results in the increase of the proportion of smaller powders. The change of interval between plasma gun and the self-consuming electrode has a little effect on the granularity distribution, also the fractal dimension of the granularity distribution changed a little correspondingly.
基金Project supported by the National Natural Science Foundation of China(51564015)
文摘Al-Cu-Y alloys were prepared by molten salt electrolysis in fluoride-oxide system composed of electrolyte（Na3 AlF6-AlF3-LiF-MgF2） and oxide（Al2 O3-CuO-Y2 O3）. Cathodic reduction process of Al2 O3,CuO and Y2 O3 were analyzed by cyclic voltammetry and chronoamperometry. Components and phase composition of alloy samples prepared by potentiostatic electrolysis were characterized by scanning electron microscopy and energy dispersive spectroscopy. The results show that the Al-Cu-Y alloy can be prepared in the AIF3-NaF-5 wt%LiF-5 wt%MgF2（NaF/AlF3 = 2.2, molecular ratio） eutectic system with mixed oxide（Al2 O3-CuO-Y2 O3） through 2 h at the conditions of a temperature of 1208 K, cell voltage3.0 V, cathode current density 0.7 A/cm^2. Al（Ⅲ） and Cu（Ⅱ） ions can be reduced to zero valence Al（0） and Cu（0） directly on carbonaceous electrode surface by instantaneous nucleation, respectively, the reduction process is controlled by diffusion. The reduction potential of Y（Ⅲ） ions is close to the active ions of fluoride melts, but strengthened phase AI3 Y can be formed through electrochemical reduction and alloyed process with active Al（Ⅲ） and Cu（Ⅱ） ions, meanwhile, the Al2 Cu and Al3 Y phases are distributed at the grain boundary of Al matrix.
文摘The electrode kinetics of cerium on aluminium electrode and its effects on the behavior of the lithium-aluminium anode were studied by using cyclic voltammetry and chronoamperometry. The electrochemical properties and physical behavior of lithium-aluminium anode were improved by adding cerium into aluminium before lithium was deposited. Some parameters for preparing lithium-aluminium electrodes were also given.
