Lithium(Li)is a promising candidate for nextgeneration battery anode due to its high theoretical specific capacity and low reduction potential.However,safety issues derived from the uncontrolled growth of Li dendrite ...Lithium(Li)is a promising candidate for nextgeneration battery anode due to its high theoretical specific capacity and low reduction potential.However,safety issues derived from the uncontrolled growth of Li dendrite and huge volume change of Li hinder its practical application.C onstructing dendrite-free composite Li anodes can significantly alleviate the above problems.Copper(Cu)-based materials have bee n widely used as substrates of the composite electrodes due to their chemical stability,excellent conductivity,and good mechanical strength.Copper/lithium(Cu/Li)composite anodes significantly regulate the local current density and decrease Li nucleation overp otential,realizing the uniform and dendrite-free Li deposition.In this review,Cu/Li composite methods including electrodeposition,melting infusion,and mechanical rolling are systematically summarized and discussed.Additionally,design strategies of Cu-based current collectors for high performance Cu/Li composite anodes are illustrated.General challenges and future development for Cu/Li composite anodes are presented and postulated.We hope that this review can provide a comprehensive understanding of Cu/Li composite methods of the latest development of Li metal anode and stimulate more research in the future.展开更多
The composite powders,Sn nanoparticles embedded into the porous hydrogel-derived carbon(Sn@PHDC),were successfully prepared by polymerization and calcination processes,and the characterization results confirmed that S...The composite powders,Sn nanoparticles embedded into the porous hydrogel-derived carbon(Sn@PHDC),were successfully prepared by polymerization and calcination processes,and the characterization results confirmed that Sn nanoparticles were homogeneously dispersed in the porous hydrogel-derived pyrolytic carbon.The coin cell assembled with the Sn@PHDC-50 composite electrode presented good cyclic stability and rate performance when the weight ratio of Sn nanoparticles to hydrogel-derived pyrolytic carbon was maintained at 1:1.Moreover,the Sn@PHDC-50 electrode manifested a lower charge transfer resistance of 58.57 Ω and a higher lithium ions diffusion coefficient of 1.117×10^(-14) cm^(2)·s^(-1) than pure Sn and other Sn@PHDC electrodes.Those improvements can be partly ascribed to the fact that the hydrogelderived pyrolytic c arbon matrix can release the volume strain and enhance the electronic conductivity of the composite electrode,and partly to the fact that the porous hydrogelderived pyrolytic carbon matrix can suppress agglomerations of Sn nanoparticles and shorten Li^(+) diffusion paths.This work may provide a new appro ach for the improvement of Sn-based anode materials for lithium-ion batteries.展开更多
An A1/Pb-0.3%Ag alloy composite anode was produced via composite casting. Its electrocatalytic activity for the oxygen evolution reaction and corrosion resistance was evaluated by anodic polarization curves and accele...An A1/Pb-0.3%Ag alloy composite anode was produced via composite casting. Its electrocatalytic activity for the oxygen evolution reaction and corrosion resistance was evaluated by anodic polarization curves and accelerated corro- sion test, respectively. The microscopic morphologies of the anode section and anodic oxidation layer during accelerated corrosion test were obtained by scanning electron microscopy. It is found that the composite anode （hard anodizing） dis- plays a more compact interracial combination and a better adhesive strength than plating tin. Compared with industrial Pb-0.3%Ag anodes, the oxygen evolution overpotentials of A1/Pb-0.3%Ag alloy （hard anodizing） and A1/Pb-0.3%Ag alloy （plating tin） at 500 A.m-2 were lower by 57 and 14 mV, respectively. Furthermore, the corrosion rates of Pb-0.3%Ag alloy, A1/Pb-0.3%Ag alloy （hard anodizing）, and A1/Pb-0.3%Ag alloy （plating tin） were 13.977, 9.487, and 11.824 g.m-2.h-1, respectively, in accelerated corrosion test for 8 h at 2000 A-m-2. The anodic oxidation layer of A1/Pb-0.3%Ag alloy （hard anodizing） is more compact than Pb-0.3%Ag alloy and A1/Pb-0.3%Ag alloy （plating tin） after the test.展开更多
The necessity to explore high-efficiency and high-value utilization strategy for biomass-waste is desirable.Herein,the strategy for direct conversion biomass-waste(rice husks) to Si/C composite structure anode was bui...The necessity to explore high-efficiency and high-value utilization strategy for biomass-waste is desirable.Herein,the strategy for direct conversion biomass-waste(rice husks) to Si/C composite structure anode was built.The Si/C composite materials were successfully obtained via the typical thermal reduction with magnesium,and the Si nanopa rticle was uniformly embedded in carbon frame,as revealed by Raman,X-ray diffraction(XRD) and transmission electron microscope(TEM) measurement.The carbon structure among rice husks was effectively used as a protective layer to accommodate the volume variation of Si anode during the repeated lithiation/delithiation process.Benefitting from the structure design,the batteries show a superior electrochemical stability with the capacity retention rate above 90% after 150 cycles at the charge/discha rge rate of 0.5 C(1 C=600 mAh/g),and hold a high charge capacity of 420.7 mAh/g at the rate of 3 C.Therefore,our finding not only provides a promising design strategy for directly conversion biomass-waste to electrochemical storage materials but broadens the high-efficiency utilization method for other biomass by-products.展开更多
Homogeneous co-precipitation and hydrothermal treatment were used to prepare nano- and highly dispersed Ni O/YSZ(yttria-stabilized zirconia) composite powders. Composite powders of size less than 100 nm were successfu...Homogeneous co-precipitation and hydrothermal treatment were used to prepare nano- and highly dispersed Ni O/YSZ(yttria-stabilized zirconia) composite powders. Composite powders of size less than 100 nm were successfully prepared. This process did not require separate sintering of the YSZ and Ni O to be used as the raw materials for solid oxide fuel cells. The performance of a cell fabricated using the new powders(max.power density ~0.87 W/cm^2) was higher than that of a cell fabricated using conventional powders(max. power density ~0.73 W/cm^2). Co-precipitation and hydrothermal treatment proved to be very effective processes for reducing cell production costs as well as improving cell performance.展开更多
Geopolymers have been developed to various catalysts due to their advantages.However,low conductivity restricts their application in the electrocatalysis field.In this study,anα-Fe_(2)O_(3)/circulating fluidized bed ...Geopolymers have been developed to various catalysts due to their advantages.However,low conductivity restricts their application in the electrocatalysis field.In this study,anα-Fe_(2)O_(3)/circulating fluidized bed fly ash based geopolymer(CFAG)composite anode was fabricated using a facile dip-coating method by loadingα-Fe_(2)O_(3) in the matrix of CFAG.The effects ofα-Fe_(2)O_(3) content on the composition,surface morphology and electrochemical performance ofα-Fe_(2)O_(3)/CFAG composite anode were investigated.The X-ray diffraction(XRD)and scanning electron microscope(SEM)results demonstrated thatα-Fe_(2)O_(3) was successfully inlaid with the surface of amorphous CFAG matrix.The electrochemical measurements indicated thatα-Fe_(2)O_(3)/CFAG composite anode had higher oxygen evolution potential,greater electrochemical activity area,and smaller electrochemical impedance than CFAG.The as-prepared composite anode was applied for electrocatalytic degradation of indigo carmine dye wastewater.It was discovered that the highest degradation efficiency over 10α-Fe_(2)O_(3)/CFAG reached up 92.6%,and the degradation of indigo carmine followed pseudo-first-order kinetics.Furthermore,10α-Fe_(2)O_(3)/CFAG composite anode presented excellent stability after five cycles.The active hydroxyl radical was generated over theα-Fe_(2)O_(3)/CFAG composite anode,which acted as strong oxidizing agents in the electrocatalytic degradation process.展开更多
The properties of Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC-ZrO2 composite anode for zinc electrowinning were investigated. The electrochemical performance was studied by Tafel polarization curves（Tafel）, e...The properties of Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC-ZrO2 composite anode for zinc electrowinning were investigated. The electrochemical performance was studied by Tafel polarization curves（Tafel）, electrochemical impedance spectroscopy（EIS） and corrosion rate obtained in an acidic zinc sulfate electrolyte solution. Scanning electron microscopy（SEM）, X-ray diffraction（XRD）, and energy dispersive X-ray spectroscopy（EDXS） were used to observe the microstructural features of coating. Anodes of Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2, Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC, Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-ZrO2, and Pb-1%Ag anodes were also researched. The results indicated that the Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC-ZrO2 showed the best catalytic activity and corrosion resistant performance; the intensity of diffraction peak exhibited the highest value as well as a new PbWO4 phase; the content of WC and ZrO2 in coating showed the highest value as well as the finest grain size.展开更多
The graphene/mesocarbon microbead(MCMB)composite is assessed as an anode material with a high capacity for lithium-ion batteries.The composite electrode exhibits improved cycling stability and rate capability,deliveri...The graphene/mesocarbon microbead(MCMB)composite is assessed as an anode material with a high capacity for lithium-ion batteries.The composite electrode exhibits improved cycling stability and rate capability,delivering a high initial charge/discharge capacity of 421.4 mA·h/g/494.8 mA·h/g as well as an excellent capacity retention over 500 cycles at a current density of 40 mA/g.At a higher current density of 800 mA/g,the electrode still retains 35%of its initial capacity which exceeds the capacity retention of pure graphene or MCMB reference electrodes.Cyclic voltammetry and electrochemical impedance spectroscopy reveal that the composite electrode favors electrochemical kinetics as compared with graphene and MCMB separately.Superior electrochemical properties suggest a strong synergetic effect between highly conductive graphene and MCMB.展开更多
As lithium(Li)-ion batteries expand their applications,operating over a wide temperature range becomes increasingly important.However,the lowtemperature performance of conventional graphite anodes is severely hampered...As lithium(Li)-ion batteries expand their applications,operating over a wide temperature range becomes increasingly important.However,the lowtemperature performance of conventional graphite anodes is severely hampered by the poor diffusion kinetics of Li ions(Li^(+)).Here,zinc oxide(ZnO) nanoparticles are incorporated into the expanded graphite to improve Li^(+)diffusion kinetics,resulting in a significant improvement in lowtemperature performance.The ZnO-embedded expanded graphite anodes are investigated with different amounts of ZnO to establish the structurecharge storage mechanism-performance relationship with a focus on lowtemperature applications.Electrochemical analysis reveals that the ZnOembedded expanded graphite anode with nano-sized ZnO maintains a large portion of the diffusion-controlled charge storage mechanism at an ultra-low temperature of-50℃ Due to this significantly enhanced Li^(+)diffusion rate,a full cell with the ZnO-embedded expanded graphite anode and a LiNi_(0.88)Co_(0.09)Al_(0.03)O_(2)cathode delivers high capacities of 176 mAh g^(-1)at20℃ and 86 mAh g^(-1)at-50℃ at a high rate of 1 C.The outstanding low-temperature performance of the composite anode by improving the Li^(+)diffusion kinetics provides important scientific insights into the fundamental design principles of anodes for low-temperature Li-ion battery operation.展开更多
Solid-state electrolytes(SSEs)are a solution to safety issues related to flammable organic electrolytes for Li batteries.Insufficient contact between the anode and SSE results in high interface resistance,thus causing...Solid-state electrolytes(SSEs)are a solution to safety issues related to flammable organic electrolytes for Li batteries.Insufficient contact between the anode and SSE results in high interface resistance,thus causing the batteries to exhibit high charging and discharging overpotentials.Recently,we reduced the overpotential of Li stripping and plating by introducing a high proportion of dual-conductive phases into a composite anode.The current study investigates the interface resistance and stability of a composite electrode modified with Zn and a lower proportion of dual-conductive phases.Zn-cation-adsorbed Prussian blue is synthesized as an intermediate component for a Zn-modified composite electrode(Li-FeZnNC).The Li-FeZnNC symmetric cell presents a lower interface resistance and overpotential compared with Li-FeNC(without Zn modification)and Li-symmetric cells.The Li-FeZnNC symmetric cell shows high electrochemical stability during Li stripping and plating at different current densities and high stability for 200 h.Full batteries with a Li-FeZnNC composite anode,garnet-type SSE,and LiFePO4 cathode show low charging and discharging overpotentials,a capacity of 152 mAh g^(−1),and high stability for 200 cycles.展开更多
The escalating demand for fast-charging lithium-ion batteries(LIBs)has mirrored the rapid proliferation and widespread adoption of electric vehicles and portable electronic devices.Nonetheless,the sluggish diffusion k...The escalating demand for fast-charging lithium-ion batteries(LIBs)has mirrored the rapid proliferation and widespread adoption of electric vehicles and portable electronic devices.Nonetheless,the sluggish diffusion kinetics of lithium ions and electrode degradation in conventional graphite-based anodes pose formidable hurdles in achieving optimal fast-charging capabilities for LIBs.To overcome these challenges,the innovative concept of fast-charging composite anodes,a paradigm shift from traditional single-component designs,has emerged as a promising avenue to enhance the overall performance of LIBs under rapid charging conditions.This paper provides a comprehensive review of the recent advancements in fast-charging composite anodes for LIBs,with a pivotal emphasis on the design principles and material selection strategies employed in various composite anode formulations.Furthermore,it outlines the future prospects and research trajectories in this burgeoning field,offering insights into potential breakthroughs and directions for further exploration.展开更多
Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials ...Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials for SIBs are mainly used as cathodes because of their relatively high redox potentials(>1 V).Organic electrodes with low redox potential that can be used as anode are rare.Herein,a novel organic anode material (tetrasodium 1,4,5,8-naphthalenetetracarboxylate,Na_(4)TDC) has been developed with low redox potential (<0.7 V) and excellent cyclic stability.Its three-sodium storage mechanism was demonstrated with various in-situ/ex-situ spectroscopy and theoretical calculations,showing a high capacity of 208 mAh/g and an average decay rate of merely 0.022%per cycle.Moreover,the Na_(4)TDC-hard carbon composite can further acquire improved capacity and cycling stability for 1200 cycles even with a high mass loading of up to 20 mg cm^(-2).By pairing with a thick Na_(3)V_(2)(PO_(4))_(3)cathode (20.6 mg cm^(-2)),the as-fabricated full cell exhibited high operating voltage (2.8 V),excellent rate performance and cycling stability with a high capacity retention of 88.7% after 200 cycles,well highlighting the Na_(4)TDC anode material for SIBs.展开更多
The lithium(Li) metal anode is an integral component in an emerging high-energy-density rechargeable battery.A composite Li anode with a three-dimensional(3 D) host exhibits unique advantages in suppressing Li dendrit...The lithium(Li) metal anode is an integral component in an emerging high-energy-density rechargeable battery.A composite Li anode with a three-dimensional(3 D) host exhibits unique advantages in suppressing Li dendrites and maintaining dimensional stability.However,the fundamental understanding and regulation of solid electrolyte interphase(SEI),which directly dictates the behavior of Li plating/stripping,are rarely researched in composite Li metal anodes.Herein,the interaction between a polar polymer host and solvent molecules was proposed as an emerging but effective strategy to enable a stable SEI and a uniform Li deposition in a working battery.Fluoroethylene carbonate molecules in electrolytes are enriched in the vicinity of a polar polyacrylonitrile(PAN) host due to a strong dipole-dipole interaction,resulting in a LiF-rich SEI on Li metal to improve the uniformity of Li deposition.A composite Li anode with a PAN host delivers 145 cycles compared with 90 cycles when a non-polar host is employed.Moreover,60 cycles are demonstrated in a 1:0 Ah pouch cell without external pressure.This work provides a fresh guidance for designing practical composite Li anodes by unraveling the vital role of the synergy between a 3 D host and solvent molecules for regulating a robust SEI.展开更多
A stable lithium-metal anode is critical for high performance lithium-metal batteries. However, heterogeneous Li plating/stripping may induce lithium dendrites formation on bare lithium-metal anode, which lowers the c...A stable lithium-metal anode is critical for high performance lithium-metal batteries. However, heterogeneous Li plating/stripping may induce lithium dendrites formation on bare lithium-metal anode, which lowers the cell Coulombic efficiency and weakens battery safety. We found that bare Li metal surface becomes bumpy and cratered with numerous pits formation during Li stripping. These pits enhance electric field distortion and heterogeneous ion distribution during plating. Li plating preferentially happens on the edge of the pits, intensifying the voltage variation and Li dendrites growth, which leads to the cell rapid death or separator piercing. Herein, we propose a facile and mass-producible method to homogenize Li plating/stripping via adding lithiophilic particles into Li metal. Zinc particles were uniformly pressed in Li metal by a facile and scalable physical strategy of “rolling”, and transformed into LiZn alloy in situ through Li-Zn alloying at room temperature in a few minutes. The critical role of modified LiZn/Li composite anode in stabilizing electrode surface was revealed by both electrochemical test and simulation. Compared with bare Li anode, the evenly dispersed LiZn alloy particles in Li metal can effectively regulate the Li plating/stripping on electrode surface, reducing deepness of pits during stripping and directionally inducing Li plating to maintain electrode surface stability. On this basis, the pits depth of LiZn/Li composite during Li stripping is reduced to ∼ 15 μm, which is much shallower than that of bare Li metal of ∼ 40 μm. The LiZn/Li composite electrode can stably cycle for 600 h under Li plating/stripping capacity of 1 mAh·cm−2 and current density of 1 mA·cm−2 without any short circuit. Furthermore, assembled LiZn/Li||LiFePO4 full cell presents better cycling stability and rate performances than that of based on bare Li anode.展开更多
In order to address the issues of low initial Coulombic efficiency of SiO_(x)-C composite anode due to the formation of solid electrolyte interphase,irreversible conversion reaction,and large volume change,the prelith...In order to address the issues of low initial Coulombic efficiency of SiO_(x)-C composite anode due to the formation of solid electrolyte interphase,irreversible conversion reaction,and large volume change,the prelithiation method using metal lithium has been employed as one of effective solutions.However,violent side reactions with liquid electrolyte for prelithiation lead to low prelithiation efficiency and induce poor interface between the SiO_(x)-C electrode and liquid electrolyte.Here,a new prelithiation method with so called solid-state corrosion of lithium is developed.By replacing liquid electrolyte with solid-state electrolyte of carbon-incorporated lithium phosphorus oxynitride(LiCPON),not only various side reactions associated with metal lithium are avoided,but also the perfect interface is achieved from the decomposition products of LiCPON.The successful implementation of solid-state corrosion prelithiation can be confirmed by changes in optical image,scanning electron microscopy,and X-ray diffraction.Compared with pristine electrode,the initial Coulombic efficiency of the prelithiated electrode using solid electrolyte can be increased by about 10%,reaching 98.6%in half cell and 88.9%in full cell.Compared with prelithiated electrode using liquid electrolyte,the prelithiation efficiency of the prelithiated anode with solid-state corrosion can be increased from 25.7%to 82.8%.Solid-state corrosion of lithium is expected to become a useful method for prelithiation of SiO_(x)-C composite electrode with high initial Coulombic efficiency and large prelithiation efficiency.展开更多
A new type of high efficient Ti composite anodes for electrodeposition of MnO 2 was successfully developed and was widely satisfied with production in many factories in China. The process parameters of electrolysis i...A new type of high efficient Ti composite anodes for electrodeposition of MnO 2 was successfully developed and was widely satisfied with production in many factories in China. The process parameters of electrolysis in using the composite anodes were optimized and discussed.展开更多
Nb_2O_5/C nanosheets are successfully prepared through a mixing process and followed by heating treatment.Such Nb_2O_5/C based electrode exhibits high rate performance and remarkable cycling ability,showing a high and...Nb_2O_5/C nanosheets are successfully prepared through a mixing process and followed by heating treatment.Such Nb_2O_5/C based electrode exhibits high rate performance and remarkable cycling ability,showing a high and stable specific capacity of ~380mAhg^（-1） at the current density of 50 mAg^（-1）（much higher than the theoretical capacity of Nb_2O_5）.Further more,at a current density of 500mAg^（-1）,the nanocomposites electrode still exhibits a specific capacity of above 150 mAh g^（-1） after 100 cycles.These results suggest the Nb_2O_5/C nanocomposite is a high performance anode material for lithium-ion batteries.展开更多
Silicon-based material is considered to be one of the most promising anodes for the next-generation lithium-ion batteries(LIBs)due to its rich sources,nontoxicity,low cost and high theoretical specific capacity.Howeve...Silicon-based material is considered to be one of the most promising anodes for the next-generation lithium-ion batteries(LIBs)due to its rich sources,nontoxicity,low cost and high theoretical specific capacity.However,it cannot maintain a stable electrode structure during repeated charge/discharge cycles,and therefore long cycling life is difficult to be achieved.To address this problem,herein a simple and efficient method is developed for the fabrication of an integrated composite anode consisting of SiO-based active material and current collector,which exhibits a core-shell structure with nitrogen-doped carbon coating on SiO/P micro-particles.Without binder and conductive agent,the volume expansion of SiO active material in the integrated composite anode is suppressed to prevent its pulverization.At a current density of 500 mA·g−1,this integrated composite anode exhibits a reversible specific capacity of 458 mA·h·g−1 after 200 cycles.Furthermore,superior rate performance and cycling stability are also achieved.This work illustrates a potential method for the fabrication of integrated composite anodes with superior electrochemical properties for high-performance LIBs.展开更多
Na–CO_(2) batteries recently are emerging as promising energy-storage devices due to the abundance of Na in the earth’s crust and the clean utilization of greenhouse gas CO_(2) .However,similar to metallic Li,metall...Na–CO_(2) batteries recently are emerging as promising energy-storage devices due to the abundance of Na in the earth’s crust and the clean utilization of greenhouse gas CO_(2) .However,similar to metallic Li,metallic Na also suffers from a serious issue of dendrite growth upon repeated cycling,while a facile method to solve this issue is still lacking.In this work,we report an effective,environmentally friendly method to inhibit Na dendrite growth by in situ constructing a stable,NaF-rich solid electrolyte interface(SEI)layer on metallic Na via adding a small amount(~3 wt%)of fluorinated graphene(FG)in bulk Na.Inspired by the forging processing,a uniform Na/FG composite was obtained by melting and repetitive FG-adsorbing/hammering processes.The Na/FG–Na/FG half cell exhibits a low voltage hysteresis of 110–140 mV over 700 h at a current density up to 5 mA cm^(-2) with an areal capacity as high as 5 mAh cm^(-2).Na–CO_(2) full cell with the Na/FG anode is able to sustain a stable cycling of 391 cycles at a limited capacity of 1000 mAh g^(-1).Long cycle life of the cell can be attributed to the protecting effect of the in situ fabricated NaF-rich SEI layer on metallic Na.Both experiments and density functional theory(DFT)calculations confirm the formation of the NaF-rich SEI layer.The inhibition effect of the NaF-rich SEI layer for Na dendrites is verified by in situ optical microscopy observations.展开更多
In order to search for a suitable anode material used in zinc electrowinning in place of Pb-Ag alloy,Al/Pb-PANI（polyaniline）-WC（tungsten carbide） composite inert anodes were prepared on aluminum alloy substrate by...In order to search for a suitable anode material used in zinc electrowinning in place of Pb-Ag alloy,Al/Pb-PANI（polyaniline）-WC（tungsten carbide） composite inert anodes were prepared on aluminum alloy substrate by double pulse electrodeposition（DPE） of PANI and WC particles with Pb2＋ from an original plating bath.Thereafter,anodic polarization curves,cyclic voltammetry curves and Tafel polarization curves for the composite inert anodes obtained under different PANI concentrations in the original plating bath were measured,and the microstructural features were also investigated by scanning electron microscopy（SEM）.The results show that Al/Pb-PANI-WC composite inert anode obtained under PANI concentration of 20 g/L in the original plating bath possesses uniform microstructures and composition distributions,higher electrocatalytic activity,better reversibility of electrode reaction and corrosion resistance in a synthetic zinc electrowinning electrolyte of 50 g/L Zn2＋,150 g/L H2SO4 at 35 °C.Compared with Pb-1%Ag alloy,the overpotential of oxygen evolutions for the composite inert anode are decreased by 185 mV and 166 mV,respectively,under 500 A/m2 and 1000 A/m2.展开更多
基金supported by the National Key Research and Development Program of China(No.2021YFB2500200)the National Natural Science Foundation of China(No.52302243)China Postdoctoral Science Foundation(Nos.2022M721029 and 2022M721030)。
文摘Lithium(Li)is a promising candidate for nextgeneration battery anode due to its high theoretical specific capacity and low reduction potential.However,safety issues derived from the uncontrolled growth of Li dendrite and huge volume change of Li hinder its practical application.C onstructing dendrite-free composite Li anodes can significantly alleviate the above problems.Copper(Cu)-based materials have bee n widely used as substrates of the composite electrodes due to their chemical stability,excellent conductivity,and good mechanical strength.Copper/lithium(Cu/Li)composite anodes significantly regulate the local current density and decrease Li nucleation overp otential,realizing the uniform and dendrite-free Li deposition.In this review,Cu/Li composite methods including electrodeposition,melting infusion,and mechanical rolling are systematically summarized and discussed.Additionally,design strategies of Cu-based current collectors for high performance Cu/Li composite anodes are illustrated.General challenges and future development for Cu/Li composite anodes are presented and postulated.We hope that this review can provide a comprehensive understanding of Cu/Li composite methods of the latest development of Li metal anode and stimulate more research in the future.
基金financially supported by the National Natural Science Foundation of China (No.51874046)the Outstanding Youth Foundation of Hubei Province (No. 2020CFA090)+1 种基金Hebei Key Laboratory of Dielectric and Electrolyte Functional Material,Northeastern University at Qinhuangdao (No. HKDEFM2021202)the Young Top-notch Talent Cultivation Program of Hubei Province。
文摘The composite powders,Sn nanoparticles embedded into the porous hydrogel-derived carbon(Sn@PHDC),were successfully prepared by polymerization and calcination processes,and the characterization results confirmed that Sn nanoparticles were homogeneously dispersed in the porous hydrogel-derived pyrolytic carbon.The coin cell assembled with the Sn@PHDC-50 composite electrode presented good cyclic stability and rate performance when the weight ratio of Sn nanoparticles to hydrogel-derived pyrolytic carbon was maintained at 1:1.Moreover,the Sn@PHDC-50 electrode manifested a lower charge transfer resistance of 58.57 Ω and a higher lithium ions diffusion coefficient of 1.117×10^(-14) cm^(2)·s^(-1) than pure Sn and other Sn@PHDC electrodes.Those improvements can be partly ascribed to the fact that the hydrogelderived pyrolytic c arbon matrix can release the volume strain and enhance the electronic conductivity of the composite electrode,and partly to the fact that the porous hydrogelderived pyrolytic carbon matrix can suppress agglomerations of Sn nanoparticles and shorten Li^(+) diffusion paths.This work may provide a new appro ach for the improvement of Sn-based anode materials for lithium-ion batteries.
基金financially supported by the National Natural Science Foundation of China(No.51004056)the Opening Foundation of the Key Laboratory of Inorganic Coating Materials,Chinese Academy of Sciences(No.KKZ6201152009)+2 种基金the Specialized Research Fund for the Doctoral Program of Higher Education(No.20125314110011)the Applied Basic Research Foundation of Yunnan Province,China(No.2010ZC052)the Analysis and Testing Foundation of Kunming University of Science and Technology(Nos.2010203 and 2011173)
文摘An A1/Pb-0.3%Ag alloy composite anode was produced via composite casting. Its electrocatalytic activity for the oxygen evolution reaction and corrosion resistance was evaluated by anodic polarization curves and accelerated corro- sion test, respectively. The microscopic morphologies of the anode section and anodic oxidation layer during accelerated corrosion test were obtained by scanning electron microscopy. It is found that the composite anode （hard anodizing） dis- plays a more compact interracial combination and a better adhesive strength than plating tin. Compared with industrial Pb-0.3%Ag anodes, the oxygen evolution overpotentials of A1/Pb-0.3%Ag alloy （hard anodizing） and A1/Pb-0.3%Ag alloy （plating tin） at 500 A.m-2 were lower by 57 and 14 mV, respectively. Furthermore, the corrosion rates of Pb-0.3%Ag alloy, A1/Pb-0.3%Ag alloy （hard anodizing）, and A1/Pb-0.3%Ag alloy （plating tin） were 13.977, 9.487, and 11.824 g.m-2.h-1, respectively, in accelerated corrosion test for 8 h at 2000 A-m-2. The anodic oxidation layer of A1/Pb-0.3%Ag alloy （hard anodizing） is more compact than Pb-0.3%Ag alloy and A1/Pb-0.3%Ag alloy （plating tin） after the test.
基金The National Natural Science Foundation of China(Nos.51803054,51772093)the Natural Science Foundation of Hunan province(Nos.2019JJ20010,2020JJ3022,2019JJ50223)+1 种基金the“Double first-class”School Construction Project(No.SYL201802008)Outstanding Youth Foundation(No.19B270)from Education Department of Hunan Province。
文摘The necessity to explore high-efficiency and high-value utilization strategy for biomass-waste is desirable.Herein,the strategy for direct conversion biomass-waste(rice husks) to Si/C composite structure anode was built.The Si/C composite materials were successfully obtained via the typical thermal reduction with magnesium,and the Si nanopa rticle was uniformly embedded in carbon frame,as revealed by Raman,X-ray diffraction(XRD) and transmission electron microscope(TEM) measurement.The carbon structure among rice husks was effectively used as a protective layer to accommodate the volume variation of Si anode during the repeated lithiation/delithiation process.Benefitting from the structure design,the batteries show a superior electrochemical stability with the capacity retention rate above 90% after 150 cycles at the charge/discha rge rate of 0.5 C(1 C=600 mAh/g),and hold a high charge capacity of 420.7 mAh/g at the rate of 3 C.Therefore,our finding not only provides a promising design strategy for directly conversion biomass-waste to electrochemical storage materials but broadens the high-efficiency utilization method for other biomass by-products.
基金supported by Basic Science Research Program through the National Research Foundation of Korea (NRF) funded by the Ministry of Education, Science and Technology (2012R1A1A1013782)a fostering project funded by the Ministry of Education, Science and Technology (MEST)
文摘Homogeneous co-precipitation and hydrothermal treatment were used to prepare nano- and highly dispersed Ni O/YSZ(yttria-stabilized zirconia) composite powders. Composite powders of size less than 100 nm were successfully prepared. This process did not require separate sintering of the YSZ and Ni O to be used as the raw materials for solid oxide fuel cells. The performance of a cell fabricated using the new powders(max.power density ~0.87 W/cm^2) was higher than that of a cell fabricated using conventional powders(max. power density ~0.73 W/cm^2). Co-precipitation and hydrothermal treatment proved to be very effective processes for reducing cell production costs as well as improving cell performance.
基金This study was supported by the National Natural Science Foundation of China(No.21676209)Key Research Development Project of Shaanxi Province(No.2019GY-137)the Cultivating Fund of Excellent Doctorate Thesis of Xi’an University of Architecture and Technology(No.6040318008).
文摘Geopolymers have been developed to various catalysts due to their advantages.However,low conductivity restricts their application in the electrocatalysis field.In this study,anα-Fe_(2)O_(3)/circulating fluidized bed fly ash based geopolymer(CFAG)composite anode was fabricated using a facile dip-coating method by loadingα-Fe_(2)O_(3) in the matrix of CFAG.The effects ofα-Fe_(2)O_(3) content on the composition,surface morphology and electrochemical performance ofα-Fe_(2)O_(3)/CFAG composite anode were investigated.The X-ray diffraction(XRD)and scanning electron microscope(SEM)results demonstrated thatα-Fe_(2)O_(3) was successfully inlaid with the surface of amorphous CFAG matrix.The electrochemical measurements indicated thatα-Fe_(2)O_(3)/CFAG composite anode had higher oxygen evolution potential,greater electrochemical activity area,and smaller electrochemical impedance than CFAG.The as-prepared composite anode was applied for electrocatalytic degradation of indigo carmine dye wastewater.It was discovered that the highest degradation efficiency over 10α-Fe_(2)O_(3)/CFAG reached up 92.6%,and the degradation of indigo carmine followed pseudo-first-order kinetics.Furthermore,10α-Fe_(2)O_(3)/CFAG composite anode presented excellent stability after five cycles.The active hydroxyl radical was generated over theα-Fe_(2)O_(3)/CFAG composite anode,which acted as strong oxidizing agents in the electrocatalytic degradation process.
基金Funded by the National Natural Science Foundation of China(Nos.51564029,51504111,51504231,51364019)the Key Project of Yunnan Province Applied Basic Research Plan of China(No.2014FA024)
文摘The properties of Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC-ZrO2 composite anode for zinc electrowinning were investigated. The electrochemical performance was studied by Tafel polarization curves（Tafel）, electrochemical impedance spectroscopy（EIS） and corrosion rate obtained in an acidic zinc sulfate electrolyte solution. Scanning electron microscopy（SEM）, X-ray diffraction（XRD）, and energy dispersive X-ray spectroscopy（EDXS） were used to observe the microstructural features of coating. Anodes of Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2, Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC, Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-ZrO2, and Pb-1%Ag anodes were also researched. The results indicated that the Al/conductive coating/α-PbO2-CeO2-TiO2/β-PbO2-WC-ZrO2 showed the best catalytic activity and corrosion resistant performance; the intensity of diffraction peak exhibited the highest value as well as a new PbWO4 phase; the content of WC and ZrO2 in coating showed the highest value as well as the finest grain size.
基金Project supported by the National Natural Science Foundation of China(No.21573239)the Guangdong Provincial Project for Science and Technology(Nos.2014TX01N14,2015B010135008,and 2016B010114003)+1 种基金the Guangzhou Municipal Project for Science and Technology(No.201509010018)the K.C.WONG Education Foundation,China。
文摘The graphene/mesocarbon microbead(MCMB)composite is assessed as an anode material with a high capacity for lithium-ion batteries.The composite electrode exhibits improved cycling stability and rate capability,delivering a high initial charge/discharge capacity of 421.4 mA·h/g/494.8 mA·h/g as well as an excellent capacity retention over 500 cycles at a current density of 40 mA/g.At a higher current density of 800 mA/g,the electrode still retains 35%of its initial capacity which exceeds the capacity retention of pure graphene or MCMB reference electrodes.Cyclic voltammetry and electrochemical impedance spectroscopy reveal that the composite electrode favors electrochemical kinetics as compared with graphene and MCMB separately.Superior electrochemical properties suggest a strong synergetic effect between highly conductive graphene and MCMB.
基金supported by an Early Career Faculty Grant from NASA’s Space Technology Research Grants Program (80NSSC18K1509)supported by the Institute for Electronics and Nanotechnology Seed Grant and performed in part at the Georgia Tech Institute for Electronics and Nanotechnology, a member of the National Nanotechnology Coordinated Infrastructure (NNCI), which was supported by the National Science Foundation (ECCS-2025462)
文摘As lithium(Li)-ion batteries expand their applications,operating over a wide temperature range becomes increasingly important.However,the lowtemperature performance of conventional graphite anodes is severely hampered by the poor diffusion kinetics of Li ions(Li^(+)).Here,zinc oxide(ZnO) nanoparticles are incorporated into the expanded graphite to improve Li^(+)diffusion kinetics,resulting in a significant improvement in lowtemperature performance.The ZnO-embedded expanded graphite anodes are investigated with different amounts of ZnO to establish the structurecharge storage mechanism-performance relationship with a focus on lowtemperature applications.Electrochemical analysis reveals that the ZnOembedded expanded graphite anode with nano-sized ZnO maintains a large portion of the diffusion-controlled charge storage mechanism at an ultra-low temperature of-50℃ Due to this significantly enhanced Li^(+)diffusion rate,a full cell with the ZnO-embedded expanded graphite anode and a LiNi_(0.88)Co_(0.09)Al_(0.03)O_(2)cathode delivers high capacities of 176 mAh g^(-1)at20℃ and 86 mAh g^(-1)at-50℃ at a high rate of 1 C.The outstanding low-temperature performance of the composite anode by improving the Li^(+)diffusion kinetics provides important scientific insights into the fundamental design principles of anodes for low-temperature Li-ion battery operation.
基金supported by the Australian Research Council Discovery Projects(grant nos.DP200103315,DP200103332,DP220103669,and DP230100685)Linkage Projects(grant no.LP220200920).
文摘Solid-state electrolytes(SSEs)are a solution to safety issues related to flammable organic electrolytes for Li batteries.Insufficient contact between the anode and SSE results in high interface resistance,thus causing the batteries to exhibit high charging and discharging overpotentials.Recently,we reduced the overpotential of Li stripping and plating by introducing a high proportion of dual-conductive phases into a composite anode.The current study investigates the interface resistance and stability of a composite electrode modified with Zn and a lower proportion of dual-conductive phases.Zn-cation-adsorbed Prussian blue is synthesized as an intermediate component for a Zn-modified composite electrode(Li-FeZnNC).The Li-FeZnNC symmetric cell presents a lower interface resistance and overpotential compared with Li-FeNC(without Zn modification)and Li-symmetric cells.The Li-FeZnNC symmetric cell shows high electrochemical stability during Li stripping and plating at different current densities and high stability for 200 h.Full batteries with a Li-FeZnNC composite anode,garnet-type SSE,and LiFePO4 cathode show low charging and discharging overpotentials,a capacity of 152 mAh g^(−1),and high stability for 200 cycles.
基金supported by the National Natural Science Foundation of China(NSFC)under Grant No.22379093the Fundamental Research Funds for the Central Universities(22X010201631,23X010301599)the Youth Teacher Initiation Plan of Shanghai Jiao Tong University(23X010502207)。
文摘The escalating demand for fast-charging lithium-ion batteries(LIBs)has mirrored the rapid proliferation and widespread adoption of electric vehicles and portable electronic devices.Nonetheless,the sluggish diffusion kinetics of lithium ions and electrode degradation in conventional graphite-based anodes pose formidable hurdles in achieving optimal fast-charging capabilities for LIBs.To overcome these challenges,the innovative concept of fast-charging composite anodes,a paradigm shift from traditional single-component designs,has emerged as a promising avenue to enhance the overall performance of LIBs under rapid charging conditions.This paper provides a comprehensive review of the recent advancements in fast-charging composite anodes for LIBs,with a pivotal emphasis on the design principles and material selection strategies employed in various composite anode formulations.Furthermore,it outlines the future prospects and research trajectories in this burgeoning field,offering insights into potential breakthroughs and directions for further exploration.
基金National Key Research and Development Program of China (2022YFB2402200)National Natural Science Foundation of China (22225201,22379028)+2 种基金Fundamental Research Funds for the Central Universities (20720220010)Shanghai Pilot Program for Basic Research–Fudan University 21TQ1400100 (21TQ009)Key Basic Research Program of Science and Technology Commission of Shanghai Municipality (23520750400)。
文摘Sodium-ion batteries (SIBs) with organic electrodes are an emerging research direction due to the sustainability of organic materials based on elements like C,H,O,and sodium ions.Currently,organic electrode materials for SIBs are mainly used as cathodes because of their relatively high redox potentials(>1 V).Organic electrodes with low redox potential that can be used as anode are rare.Herein,a novel organic anode material (tetrasodium 1,4,5,8-naphthalenetetracarboxylate,Na_(4)TDC) has been developed with low redox potential (<0.7 V) and excellent cyclic stability.Its three-sodium storage mechanism was demonstrated with various in-situ/ex-situ spectroscopy and theoretical calculations,showing a high capacity of 208 mAh/g and an average decay rate of merely 0.022%per cycle.Moreover,the Na_(4)TDC-hard carbon composite can further acquire improved capacity and cycling stability for 1200 cycles even with a high mass loading of up to 20 mg cm^(-2).By pairing with a thick Na_(3)V_(2)(PO_(4))_(3)cathode (20.6 mg cm^(-2)),the as-fabricated full cell exhibited high operating voltage (2.8 V),excellent rate performance and cycling stability with a high capacity retention of 88.7% after 200 cycles,well highlighting the Na_(4)TDC anode material for SIBs.
基金supported by the National Natural Science Foundation of China (21825501 and U1932220)the National Key Research and Development Program (2016YFA0202500)+2 种基金the Seed Fund of Shanxi Research Institute for Clean Energy (SXKYJF015)the Scientific and technological Key Project of Shanxi Province (20191102003)the Tsinghua University Initiative Scientific Research Program.
文摘The lithium(Li) metal anode is an integral component in an emerging high-energy-density rechargeable battery.A composite Li anode with a three-dimensional(3 D) host exhibits unique advantages in suppressing Li dendrites and maintaining dimensional stability.However,the fundamental understanding and regulation of solid electrolyte interphase(SEI),which directly dictates the behavior of Li plating/stripping,are rarely researched in composite Li metal anodes.Herein,the interaction between a polar polymer host and solvent molecules was proposed as an emerging but effective strategy to enable a stable SEI and a uniform Li deposition in a working battery.Fluoroethylene carbonate molecules in electrolytes are enriched in the vicinity of a polar polyacrylonitrile(PAN) host due to a strong dipole-dipole interaction,resulting in a LiF-rich SEI on Li metal to improve the uniformity of Li deposition.A composite Li anode with a PAN host delivers 145 cycles compared with 90 cycles when a non-polar host is employed.Moreover,60 cycles are demonstrated in a 1:0 Ah pouch cell without external pressure.This work provides a fresh guidance for designing practical composite Li anodes by unraveling the vital role of the synergy between a 3 D host and solvent molecules for regulating a robust SEI.
基金This work is financially supported by the China Postdoctoral Science Foundation(No.2020M672268)the National Natural Science Foundations of China(Nos.5190070667,51807180,and 52002358).
文摘A stable lithium-metal anode is critical for high performance lithium-metal batteries. However, heterogeneous Li plating/stripping may induce lithium dendrites formation on bare lithium-metal anode, which lowers the cell Coulombic efficiency and weakens battery safety. We found that bare Li metal surface becomes bumpy and cratered with numerous pits formation during Li stripping. These pits enhance electric field distortion and heterogeneous ion distribution during plating. Li plating preferentially happens on the edge of the pits, intensifying the voltage variation and Li dendrites growth, which leads to the cell rapid death or separator piercing. Herein, we propose a facile and mass-producible method to homogenize Li plating/stripping via adding lithiophilic particles into Li metal. Zinc particles were uniformly pressed in Li metal by a facile and scalable physical strategy of “rolling”, and transformed into LiZn alloy in situ through Li-Zn alloying at room temperature in a few minutes. The critical role of modified LiZn/Li composite anode in stabilizing electrode surface was revealed by both electrochemical test and simulation. Compared with bare Li anode, the evenly dispersed LiZn alloy particles in Li metal can effectively regulate the Li plating/stripping on electrode surface, reducing deepness of pits during stripping and directionally inducing Li plating to maintain electrode surface stability. On this basis, the pits depth of LiZn/Li composite during Li stripping is reduced to ∼ 15 μm, which is much shallower than that of bare Li metal of ∼ 40 μm. The LiZn/Li composite electrode can stably cycle for 600 h under Li plating/stripping capacity of 1 mAh·cm−2 and current density of 1 mA·cm−2 without any short circuit. Furthermore, assembled LiZn/Li||LiFePO4 full cell presents better cycling stability and rate performances than that of based on bare Li anode.
基金supported by the National Natural Science Foundation of China(No.22279022)the Joint Funds of the National Natural Science Foundation of China(No.U20A20336)the Tianmu Lake Institute of Advanced Energy Storage Technologies Scientist Studio Program(No.TIESSS0002).
文摘In order to address the issues of low initial Coulombic efficiency of SiO_(x)-C composite anode due to the formation of solid electrolyte interphase,irreversible conversion reaction,and large volume change,the prelithiation method using metal lithium has been employed as one of effective solutions.However,violent side reactions with liquid electrolyte for prelithiation lead to low prelithiation efficiency and induce poor interface between the SiO_(x)-C electrode and liquid electrolyte.Here,a new prelithiation method with so called solid-state corrosion of lithium is developed.By replacing liquid electrolyte with solid-state electrolyte of carbon-incorporated lithium phosphorus oxynitride(LiCPON),not only various side reactions associated with metal lithium are avoided,but also the perfect interface is achieved from the decomposition products of LiCPON.The successful implementation of solid-state corrosion prelithiation can be confirmed by changes in optical image,scanning electron microscopy,and X-ray diffraction.Compared with pristine electrode,the initial Coulombic efficiency of the prelithiated electrode using solid electrolyte can be increased by about 10%,reaching 98.6%in half cell and 88.9%in full cell.Compared with prelithiated electrode using liquid electrolyte,the prelithiation efficiency of the prelithiated anode with solid-state corrosion can be increased from 25.7%to 82.8%.Solid-state corrosion of lithium is expected to become a useful method for prelithiation of SiO_(x)-C composite electrode with high initial Coulombic efficiency and large prelithiation efficiency.
文摘A new type of high efficient Ti composite anodes for electrodeposition of MnO 2 was successfully developed and was widely satisfied with production in many factories in China. The process parameters of electrolysis in using the composite anodes were optimized and discussed.
基金supported by the National Natural Science Foundation of China(Nos.51402103 and 51302079)
文摘Nb_2O_5/C nanosheets are successfully prepared through a mixing process and followed by heating treatment.Such Nb_2O_5/C based electrode exhibits high rate performance and remarkable cycling ability,showing a high and stable specific capacity of ~380mAhg^（-1） at the current density of 50 mAg^（-1）（much higher than the theoretical capacity of Nb_2O_5）.Further more,at a current density of 500mAg^（-1）,the nanocomposites electrode still exhibits a specific capacity of above 150 mAh g^（-1） after 100 cycles.These results suggest the Nb_2O_5/C nanocomposite is a high performance anode material for lithium-ion batteries.
基金This work was supported by the National Natural Science Foundation of China (Grant Nos. 21965007, 51671062 and 51871065)the Guangxi Natural Science Foundation (Grant No. 2018GXNSFFA281005)+2 种基金the Chinesisch-Deutsche Kooperationsgruppe (Grant No. GZ1528)the Innovation Project of GUET Graduate Education (Grant Nos. 2019YCXS115 and 2019YCXS111)the Guangxi Bagui Scholar Foundation, Guangxi Advanced Functional Materials Foundation and Application Talents Small Highlands.
文摘Silicon-based material is considered to be one of the most promising anodes for the next-generation lithium-ion batteries(LIBs)due to its rich sources,nontoxicity,low cost and high theoretical specific capacity.However,it cannot maintain a stable electrode structure during repeated charge/discharge cycles,and therefore long cycling life is difficult to be achieved.To address this problem,herein a simple and efficient method is developed for the fabrication of an integrated composite anode consisting of SiO-based active material and current collector,which exhibits a core-shell structure with nitrogen-doped carbon coating on SiO/P micro-particles.Without binder and conductive agent,the volume expansion of SiO active material in the integrated composite anode is suppressed to prevent its pulverization.At a current density of 500 mA·g−1,this integrated composite anode exhibits a reversible specific capacity of 458 mA·h·g−1 after 200 cycles.Furthermore,superior rate performance and cycling stability are also achieved.This work illustrates a potential method for the fabrication of integrated composite anodes with superior electrochemical properties for high-performance LIBs.
基金supported by the National Natural Science Foundation of China(No.51572238)Zhejiang Provincial Natural Science Foundation of China under Grant no.LY19E020013Hunan Provincial Science and Technology Major Project of China(2020GK1014).
文摘Na–CO_(2) batteries recently are emerging as promising energy-storage devices due to the abundance of Na in the earth’s crust and the clean utilization of greenhouse gas CO_(2) .However,similar to metallic Li,metallic Na also suffers from a serious issue of dendrite growth upon repeated cycling,while a facile method to solve this issue is still lacking.In this work,we report an effective,environmentally friendly method to inhibit Na dendrite growth by in situ constructing a stable,NaF-rich solid electrolyte interface(SEI)layer on metallic Na via adding a small amount(~3 wt%)of fluorinated graphene(FG)in bulk Na.Inspired by the forging processing,a uniform Na/FG composite was obtained by melting and repetitive FG-adsorbing/hammering processes.The Na/FG–Na/FG half cell exhibits a low voltage hysteresis of 110–140 mV over 700 h at a current density up to 5 mA cm^(-2) with an areal capacity as high as 5 mAh cm^(-2).Na–CO_(2) full cell with the Na/FG anode is able to sustain a stable cycling of 391 cycles at a limited capacity of 1000 mAh g^(-1).Long cycle life of the cell can be attributed to the protecting effect of the in situ fabricated NaF-rich SEI layer on metallic Na.Both experiments and density functional theory(DFT)calculations confirm the formation of the NaF-rich SEI layer.The inhibition effect of the NaF-rich SEI layer for Na dendrites is verified by in situ optical microscopy observations.
基金Project (51004056) supported by the National Natural Science Foundation of ChinaProject (KKZ6201152009) supported by the Opening Foundation of Key Laboratory of Inorganic Coating Materials, ChinaProjects (2011239, 2011240) supported by Analysis and Measurement Research Fund of Kunming University of Science and Technology,China
文摘In order to search for a suitable anode material used in zinc electrowinning in place of Pb-Ag alloy,Al/Pb-PANI（polyaniline）-WC（tungsten carbide） composite inert anodes were prepared on aluminum alloy substrate by double pulse electrodeposition（DPE） of PANI and WC particles with Pb2＋ from an original plating bath.Thereafter,anodic polarization curves,cyclic voltammetry curves and Tafel polarization curves for the composite inert anodes obtained under different PANI concentrations in the original plating bath were measured,and the microstructural features were also investigated by scanning electron microscopy（SEM）.The results show that Al/Pb-PANI-WC composite inert anode obtained under PANI concentration of 20 g/L in the original plating bath possesses uniform microstructures and composition distributions,higher electrocatalytic activity,better reversibility of electrode reaction and corrosion resistance in a synthetic zinc electrowinning electrolyte of 50 g/L Zn2＋,150 g/L H2SO4 at 35 °C.Compared with Pb-1%Ag alloy,the overpotential of oxygen evolutions for the composite inert anode are decreased by 185 mV and 166 mV,respectively,under 500 A/m2 and 1000 A/m2.
