This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0...This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.1)Mo_(0.05)O_(3-δ)(B S CNM_(0.05)),Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.05)Mo_(0.1)O_(3-δ)(BSCNM_(0.1)),and Ba_(0.6)Sr_(0.4)Co_(0.85)Mo_(0.15)O_(3-δ)(BSCM)—with Mo doping contents of 5mol%,10mol%,and15mol%,respectively,were successfully prepared using the sol-gel method.The effects of Mo doping on the crystal structure,conductivity,thermal expansion coefficient,oxygen reduction reaction(ORR)activity,and electrochemical performance were systematically evaluated using X-ray diffraction analysis,thermally induced characterization,electrochemical impedance spectroscopy,and single-cell performance tests.The results revealed that Mo doping could improve the conductivity of the materials,suppress their thermal expansion effects,and significantly improve the electrochemical performance.Surface chemical state analysis using X-ray photoelectron spectroscopy revealed that 5mol%Mo doping could facilitate a high adsorbed oxygen concentration leading to enhanced ORR activity in the materials.Density functional theory calculations confirmed that Mo doping promoted the ORR activity in the materials.At an operating temperature of 600℃,the BSCNM_(0.05)cathode material exhibited significantly enhanced electrochemical impedance characteristics,with a reduced area specific resistance of 0.048Ω·cm~2,which was lower than that of the undoped BSCN matrix material by 32.39%.At the same operating temperature,an anode-supported single cell using a BSCNM_(0.05)cathode achieved a peak power density of 1477 mW·cm^(-2),which was 30.71%,56.30%,and 171.50%higher than those of BSCN,BSCNM_(0.1),and B SCM,respectively.The improved ORR activity and electrochemical performance of BSCNM_(0.05)indicate that it can be used as a cathode material in low-temperature solid oxide fuel cells.展开更多
This paper discusses numerical methods for modelling cathodic protation (CP) using Boundary ElementMethods(BEM) for CP design analysis in comparision with the traditional methods and presentsseveral mathematical model...This paper discusses numerical methods for modelling cathodic protation (CP) using Boundary ElementMethods(BEM) for CP design analysis in comparision with the traditional methods and presentsseveral mathematical models (for CP design in 3-D infinite area) solvable by using BEM withmicrocomputer.展开更多
A novel three-dimensional hierarchical WO_(3)photoelectrode was prepared by solvothermal method,and ZnO was deposited on its surface by electrochemical method.The WO_(3)/ZnWO_(4)/ZnO multiphaseheterojunction photoelec...A novel three-dimensional hierarchical WO_(3)photoelectrode was prepared by solvothermal method,and ZnO was deposited on its surface by electrochemical method.The WO_(3)/ZnWO_(4)/ZnO multiphaseheterojunction photoelectrode was prepared by further annealing treatment to explore the photoinduced cathodic protection(CP)performance.Compared with WO_(3)and ZnO,the photoinduced CP and electron storage capacity performance of WO_(3)/ZnWO_(4)/ZnO is significantly improved in 3.5%NaCl solution without adding any hole scavenger.The electron storage capacity of the WO_(3)/ZnWO_(4)/ZnO heterojunction makes it possible to continuously protect metallic materials in the dark after switching off the light,which can realize long-term and effective photoinduced CP.展开更多
Metallic pipeline corrosion poses a significant challenge in the petrochemical industry. In this study, the design and control of a stand-alone photovoltaic (PV)-powered cathodic protection (CP) system based on the im...Metallic pipeline corrosion poses a significant challenge in the petrochemical industry. In this study, the design and control of a stand-alone photovoltaic (PV)-powered cathodic protection (CP) system based on the impressed current method were investigated. The proposed CP system was applied to a 250 km long steel-buried pipeline in the Sharm El-Sheikh region of Egypt. The system design involved the numerical modeling of the anode bed for the impressed current CP (ICCP) system and the sizing of the DC power source, including the PV array and battery bank. The system was designed and controlled to deliver a constant and continuous anode current to protect the underground pipeline from corrosion during daylight and nighttime. A maximum power point tracking (MPPT) algorithm based on the fractional open-circuit voltage (FOCV) technique was implemented to maximize power extraction from the PV array. Additionally, a proportional-integral (PI) controller was optimized and employed to achieve MPPT, while another PI controller managed the anode current of the CP system. Safe charging and discharging of the system’s battery are ensured via an ON-OFF controller. The parameters of the PI controllers were optimized using the particle swarm optimization (PSO) technique. Simulation results demonstrated that the proposed CP system achieved the required protection objectives successfully.展开更多
In this study,the pure erosion behaviour of pure iron and its erosion-corrosion behaviour under different anodic polarization currents were investigated in various cathodic reactions(oxygen reduction,hydrogen ion redu...In this study,the pure erosion behaviour of pure iron and its erosion-corrosion behaviour under different anodic polarization currents were investigated in various cathodic reactions(oxygen reduction,hydrogen ion reduction,and water reduction)using a cylindrical stirring system.The corrosion-enhanced erosion(C-E)rates were determined for each condition.The results revealed that pure iron displayed similar pure erosion behaviour across all three cathodic reactions.When the cathodic reactions involve hydrogen ion reduction or water reduction,the erosion-corrosion of pure iron manifested as uniform damage,with the reduction in hardness being the main cause of the C-E in this case.Conversely,in the case of oxy-gen reduction reaction as the cathodic reaction,the erosion-corrosion presented as pitting damage,with the reduction in hardness resulting from localized concentration of anodic current and the formation of easily worn protruding flaky iron structures at the edges of the pits as the main mechanism of the C-E.Moreover,linear and exponential relationships were found between the C-E rate and the anodic current density for uniform damage and pitting damage,respectively.Finally,the concept of surface equivalent hardness was proposed,along with the establishment of a mathematical model for surface equivalent hardness based on the relationships between the C-E rate and the anodic current density.Utilizing the surface equivalent hardness enables the evaluation of the erosion rate on material surfaces considering the coupled effect.展开更多
This work presents a study on the use of cathodic protection as a measure against corrosion in pipelines.The cathodic protection,compliant with the API 5L standard,is implemented here by applying an impressed current,...This work presents a study on the use of cathodic protection as a measure against corrosion in pipelines.The cathodic protection,compliant with the API 5L standard,is implemented here by applying an impressed current,while carefully considering several essential variables,such as soil characteristics,the type and color of the pipeline material,as well as the placement and size of the anode.Therefore,it is crucial to optimize the location and values of anodic overflows or ground resistances to ensure a uniform distribution of potential across the entire structure.In this method,impressed current protection uses an auxiliary anode and an external direct current source to induce a current through the electrolyte and the pipeline,thus countering the resistance of the steel.This approach is advantageous as it allows for the adjustment of electrical characteristics,particularly current levels,to meet specific needs.The factors essential to the effectiveness of cathodic protection systems,which optimize the distribution of protection potential across the structure,largely depend on the precise management of ground resistances during anodic discharge,particularly the attenuation coefficient(α).These factors were studied,and the results obtained were presented and discussed based on their influence.展开更多
A novel and long-lasting N_(3)BD/TiO_(2) composite photoanode with stable and superior photoelectrochemical and photoelectrochemical cathodic protection(PECCP)performances was achieved by synthesizing and depositing c...A novel and long-lasting N_(3)BD/TiO_(2) composite photoanode with stable and superior photoelectrochemical and photoelectrochemical cathodic protection(PECCP)performances was achieved by synthesizing and depositing covalent organic framework(N_(3)BD)on titanium oxide(TiO_(2))nanotube arrays.The composite's increased visible light absorption capability enhanced the galvanic corrosion protection of nickel-phosphorus alloy-coated magnesium alloy(Mg/Ni)through PECCP technology.The open circuit potential(OCP)drops of the Mg/Ni electrode coupling with the N_(3)BD/TiO_(2) composite were 310 and 630 mV at dark state and under illumination,respectively.They remained relatively stable under intermittent visible light irradiation within 72 h,demonstrating excellent long-term stability.The superior photoelectrochemical and PECCP properties of the N_(3)BD/TiO_(2) are attributed to forming S-scheme heterojunctions,which effectively promote the separation and transfer of photogenerated electron-hole pairs and retain a strong redox capacity.This finding provides new insight into the design and synthesis of COF-modified photoanode with highly efficient and stable photoelectrochemical and PECCP performances.展开更多
Thefield of energy storage devices is primarily dominated by lithium-ion batteries(LIBs)due to their mature manufacturing processes and stable performance.However,immature lithium recovery technology cannot stop the co...Thefield of energy storage devices is primarily dominated by lithium-ion batteries(LIBs)due to their mature manufacturing processes and stable performance.However,immature lithium recovery technology cannot stop the continuous increase in the cost of LIBs.Along with the rapid development of electric transportation,it has become inevitable to trigger a new round of competition in alternative energy storage systems.Some monovalent rechargeable metal ion batteries(sodium ion batteries(SIBs)and potassium ion batteries(PIBs),etc.)and multi-valent rechargeable metal-ion batteries(magnesium ion batteries(MIBs),calcium ion batteries(CIBs),zinc ion batteries(ZIBs),and aluminum ion batteries(AIBs),etc.)are potential candidates,which can replace LIBs in some of the scenarios to alleviate the pressure on supply.The cathode material plays a crucial role in determining the battery capacity.Transition metal compounds dominated by layered transition metal oxides as key cathode materials for secondary batteries play an important role in the advancement of various battery energy storage systems.In summary,this manuscript aims to review and summarize the research progress on transition metal compounds used as cathodes in different metal ion batteries,with the aim of providing valuable guidance for the exploration and design of high-performance integrated battery systems.展开更多
Constructing a photoanode with both high dark-state protection performance and high stability remains a top priority for photoelectrochemical cathodic protection technology,especially in a marine environment(dark-stat...Constructing a photoanode with both high dark-state protection performance and high stability remains a top priority for photoelectrochemical cathodic protection technology,especially in a marine environment(dark-state or rainy conditions)without hole scavenging agents.In this work,we developed a class of energy-storage quasi-planar heterojunctions(WO_(3)-Nb_(2)O_(5)-ZnIn_(2)S_(4))with directional paths(low onset potential and well-matched energy band)and embedded morphology.The co-design of embedded and directional paths reduces the carrier transport energy barrier at the composite interface,and increases the interface contact area,thereby achieving highly stable and sensitive dark-state energy storage and photoelectrochemical cathodic protection performance in 3.5 wt.%NaCl solution without hole scavenging agent(Dark-state energy storage efficiency increased by 43%.For carbon steel,the performance retention rate is 99.6%after 500 cycles,the performance retention rate is 89%after 5000 s).展开更多
Coupling with high-voltage oxide cathode is the key to achieve high-energy density sulfide-based all-solid-state lithium batteries.However,the complex interfacial issues including the space charge layer effect and und...Coupling with high-voltage oxide cathode is the key to achieve high-energy density sulfide-based all-solid-state lithium batteries.However,the complex interfacial issues including the space charge layer effect and undesirable side reaction between sulfide solid-state electrolytes and oxide cathode materials are the main constraints on the development of high-performance allsolid-state lithium batteries,which lead to the continuous decay of electrochemical performance.Herein,different from the complicated coating procedure,a LiPO_(2)F_(2)additive engineering was proposed to achieve high-performance all-solid-state lithium batteries.With the introduction of LiPO_(2)F_(2)additive,a protective cathode-electrolyte interphase consisting of LiPxOyFz,LiF,and Li_(3)PO_(4)could be in situ formed to improve the interfacial stability between LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)and Li_(5.5)PS_(4.5)Cl_(1.5)(LPSC).Benefiting from this,the NCM811/LPSC/Li all-solid-state lithium battery exhibited impressive cyclic stability with a capacity retention of 85.5%after 600 cycles(at 0.5 C).Diverse and comprehensive characterization,combined with finite element simulation and density functional theory calculation fully demonstrated the effective component,interfacial stabilization function and enhanced kinetic of LiPO_(2)F_(2)-derived cathode-electrolyte interphase.This work provides not only a feasible and effective method to stabilize the cathodic interface but also worthy insight into interfacial design for high-performance all-solid-state lithium batteries.展开更多
Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the...Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the cathode side,which strictly requires the development of high voltage,high capacity,and earth-abundant cathode material.Ni-Fe-Mn ternary layered oxide has been recognized as one of the most promising standard type of cathodes.However,the composition and phase structure on high-voltage characteristics have not been well investigated.Herein,selecting the typically high-voltage cathode of P2-Na_(0.67)Ni_(0.33)Mn_(0.67)O_(2)as a parent material,we fabricate ten Ni-Fe-Mn ternary layered oxides through replacing the Ni,Mn,or both Ni and Mn by Fe.The thermodynamically stable phase diagram for those materials is presented.The electrochemical properties for all the samples are investigated in detail.Three potential Ni-Fe-Mn ternary layered oxides are picked up considering the energy density,cycle stability,kinetics,cost price,and working voltage,which demonstrate great potential for surpassing the performance of lithium iron phosphate.The related electrochemical reaction and fading mechanism are well revealed.This work provides some new foundational Ni-Fe-Mn ternary layered materials for high-voltage sodium-ion batteries.展开更多
Photogenerated electrons generated by photoexcitation of semiconductor materials can be transferred to metal materials to provide corrosion protection.Conversely,the accumulation of photogenerated holes accelerates th...Photogenerated electrons generated by photoexcitation of semiconductor materials can be transferred to metal materials to provide corrosion protection.Conversely,the accumulation of photogenerated holes accelerates the recombination of photogenerated carriers.Consequently,the development of efficient strategies for the consumption of photogenerated holes has emerged as a critical challenge in the field of photoelectrochemical cathodic protection technology.In this paper,TiO_(2)/TiOBr heterojunction photoelectrode was firstly prepared by simple hydrothermal method,and NiCo-LDH(layered double hydroxide)was further deposited on TiO_(2)/TiOBr to obtain TiO_(2)/TiOBr/NiCo-LDH photoelectrode.The construction of a heterojunction between TiO_(2)and TiOBr promotes the separation of photogenerated carriers,while the deposition of NiCo-LDH reduces the overpotential for hole oxidation.Hence,the photoinduced potential drop and photoinduced current density of TiO_(2)/TiOBr/NiCo-LDH photoelectrode coupled with 316 L stainless steel in 3.5 wt%NaCl under simulated sunlight irradiation can be up to 303 mV and 25.87μA/cm^(2),respectively.This study provides a new idea for the design and preparation of TiO_(2)-based photoelectrodes with excellent photocathodic protection under visible light.展开更多
Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical b...Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical behaviors,yet has not been unraveled.Here we propose an NH_(4)^(+)-modulated cationic solvation strategy to optimize cathodic spatial charge distribution and achieve dynamic Zn^(2+)/NH_(4)^(+)co-storage for boosting Zinc hybrid capacitors.Owing to the hierarchical cationic solvated structure in hybrid Zn(CF_(3)SO_(3))_(2)–NH_4CF_(3)SO_(3)electrolyte,high-reactive Zn^(2+)and small-hydrate-sized NH_4(H_(2)O))(4)^(+)induce cathodic interfacial Helmholtz plane reconfiguration,thus effectively enhancing the spatial charge density to activate 20%capacity enhancement.Furthermore,cathodic interfacial adsorbed hydrated NH_(4)^(+)ions afford high-kinetics and ultrastable C···H(NH_(4)^(+))charge storage process due to a much lower desolvation energy barrier compared with heavy and rigid Zn(H_(2)O)_6^(2+)(5.81 vs.14.90 eV).Consequently,physical uptake and multielectron redox of Zn^(2+)/NH_(4)^(+)in carbon cathode enable the zinc capacitor to deliver high capacity(240 mAh g^(-1)at 0.5 A g^(-1)),large-current tolerance(130 mAh g^(-1)at 50 A g^(-1))and ultralong lifespan(400,000cycles).This study gives new insights into the design of cathode–electrolyte interfaces toward advanced zinc-based energy storage.展开更多
Correction to:Nano-Micro Letters(2025)17:117 https://doi.org/10.1007/s40820-025-01660-0 Following publication of the original article[1],the authors reported that the supplementary file needed to be updated because th...Correction to:Nano-Micro Letters(2025)17:117 https://doi.org/10.1007/s40820-025-01660-0 Following publication of the original article[1],the authors reported that the supplementary file needed to be updated because they mistakenly used the incorrect version.The original article[1]has been corrected.展开更多
The effect of 10% Si （mole fraction） addition on TiAlSiN coatings was studied. Ti0.5Al0.5N, Ti0.5Al0.4Si0.1N and Ti0.55Al0.35Si0.1N coatings were deposited on WC？Co substrates by cathodic arc evaporation. The mi...The effect of 10% Si （mole fraction） addition on TiAlSiN coatings was studied. Ti0.5Al0.5N, Ti0.5Al0.4Si0.1N and Ti0.55Al0.35Si0.1N coatings were deposited on WC？Co substrates by cathodic arc evaporation. The microstructure and mechanical properties were characterized by X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, scanning electron microscopy （SEM）, nano-indentation measurement and scratch test. The mechanisms of how Si affects the properties and failure modes of TiAlSiN coatings were also discussed. The results show that the addition of 10% Si results in the formation of nc-（Ti,Al,Si）N/a-Si3N4 nano-composite structure. The hardness and toughness of TiAlSiN coatings increase, whereas the coating adhesion strength decreases. Compared with Ti0.55Al0.35Si0.1N coating, Ti0.5Al0.4Si0.1N coating has higher hardness but lower toughness. The dominant failure mode of TiAlN coating is wedging spallation due to low toughness and strong interfacial adhesion. The dominant failure mode of TiAlSiN coatings is buckling spallation due to improved toughness and weakened interfacial adhesion.展开更多
A novel type of composite electrode based on nmltiwalled carbon nanotubes coated with sheet-like cobalt hydroxide particles was used in supercapacitors. Cobalt hydroxide cathodlcally deposited fiom Co（NO3）O2 solutio...A novel type of composite electrode based on nmltiwalled carbon nanotubes coated with sheet-like cobalt hydroxide particles was used in supercapacitors. Cobalt hydroxide cathodlcally deposited fiom Co（NO3）O2 solution with carbon nanotubes as matrix exhibited large pseudo-capacitance of 322 F/g in 1 mol/L KOH. To characterize the cobalt hydroxide nanocomposite electrode, a charge-discharge cycling test, cyclic voltammetry, and an impedance test were done. This cobalt hydroxide composite exhibiting excellent pseudo-capacitive behavior （i.c. high reversibility, high specific capacitance, low impedance）, was demonstrated to be a candidate for the application of electrochemical supercapacitors. A combined capacitor consisting of cobalt hydroxide composite as a cathode and activated carbon fiber as an anode was reported. The electrochemical pcrformance of the combined capacitor was characterized by cyclic voltammetry and a dc charge/discharge test. The combined capacitor showed ideal capacitor behavior with an extended operating voltage of 1.4 V. According to the extended operating voltage, the energy density of the combined capacitor at a current density of 100 mA/cm^2 was found to be 11 Wh/kg. The combined capacitor exhibited high-energy density and stable power characteristics,展开更多
Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity c...Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity carbon nanotubes(CNT)conductive materials,and electrode thickening.However,these methods are still limited due to the limitation in the capacity of high-nickel NCM,aggregation of CNT conductive materials,and nonuniform material distribution of thick-film electrodes,which ultimately damage the mechanical and electrical integrity of the electrode,leading to a decrease in electrochemical performance.Here,we present an integrated binder-CNT composite dispersion solution to realize a high-solids-content(>77 wt%)slurry for high-mass-loading electrodes and to mitigate the migration of binder and conductive additives.Indeed,the approach reduces solvent usage by approximately 30%and ensures uniform conductive additive-binder domain distribution during electrode manufacturing,resulting in improved coating quality and adhesive strength for high-mass-loading electrodes(>12 mAh cm^(−2)).In terms of various electrode properties,the presented electrode showed low resistance and excellent electrochemical properties despite the low CNT contents of 0.6 wt%compared to the pristine-applied electrode with 0.85 wt%CNT contents.Moreover,our strategy enables faster drying,which increases the coating speed,thereby offering potential energy savings and supporting carbon neutrality in wet-based electrode manufacturing processes.展开更多
A novel trace nickel(Ni)doped tungsten(W)matrix with coated Ni on W grains was prepared by powder metallurgy method.The introduction of Ni can inhibit the reaction between W and barium-calcium aluminates(Ba-Ca alumina...A novel trace nickel(Ni)doped tungsten(W)matrix with coated Ni on W grains was prepared by powder metallurgy method.The introduction of Ni can inhibit the reaction between W and barium-calcium aluminates(Ba-Ca aluminates)during the impregnation process of the matrix.After cathode activation,the surface Ba:O molar ratio is 0.88:1.00,much higher than the Ba dispenser cathode without Ni doping.The XPS results of the cathode surface showed that the metallic Ba appeared on the activated cathode surface,forming dipoles with oxygen,and effectively reducing the cathode surface work function.The pulse electron emission current density at 1100℃_(b)(brightness temperature)was 18.26 A/cm^(2),and the calculated work function was 1.97 eV.It has a low evaporation rate and the accelerated lifetime test predict a lifetime of over 160000 h.First-principles calculations showed that the charge transfer and dipole moment in the NiW-BaO system were both increased compared to the Ba dispenser cathode,thus improving the emission performance of the Ni-W mixed matrix cathode.展开更多
Long-life energy storage batteries are integral to energy storage systems and electric vehicles,with lithium-ion batteries(LIBs)currently being the preferred option for extended usage-life energy storage.To further ex...Long-life energy storage batteries are integral to energy storage systems and electric vehicles,with lithium-ion batteries(LIBs)currently being the preferred option for extended usage-life energy storage.To further extend the life span of LIBs,it is essential to intensify investments in battery design,manufacturing processes,and the advancement of ancillary materials.The pursuit of long durability introduces new challenges for battery energy density.The advent of electrode material offers effective support in enhancing the battery’s long-duration performance.Often underestimated as part of the cathode composition,the binder plays a pivotal role in the longevity and electrochemical performance of the electrode.Maintaining the mechanical integrity of the electrode through judicious binder design is a fundamental requirement for achieving consistent long-life cycles and high energy density.This paper primarily concentrates on the commonly employed cathode systems in lithium-ion batteries,elucidates the significance of binders for both,discusses the application status,strengths,and weaknesses of novel binders,and ultimately puts forth corresponding optimization strategies.It underscores the critical function of binders in enhancing battery performance and advancing the sustainable development of lithium-ion batteries,aiming to offer fresh insights and perspectives for the design of high-performance LIBs.展开更多
Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from...Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from the cathode side.These challenges lead to poor cycle stability and severe self-discharge.From the fabrication and cost point of view,it is technologically more viable to deploy electrolyte engineering than electrode protection strategies.More importantly,a synchronous method for modulation of both cathode and anode is pivotal,which has been often neglected in prior studies.In this work,cationic poly(allylamine hydrochloride)(Pah^(+))is adopted as a low-cost dual-function electrolyte additive for ZIBs.We elaborate the synchronous effect by Pah^(+)in stabilizing Zn anode and immobilizing polyiodide anions.The fabricated Zn-iodine coin cell with Pah^(+)(ZnI_(2) loading:25 mg cm^(−2))stably cycles 1000 times at 1 C,and a single-layered 3.4 cm^(2) pouch cell(N/P ratio~1.5)with the same mass loading cycles over 300 times with insignificant capacity decay.展开更多
基金financially supported by the National Natural Science Foundation of China(No.22309067)the Open Project Program of the State Key Laboratory of Materials-Oriented Chemical Engineering,China(No.KL21-05)the Marine Equipment and Technology Institute,Jiangsu University of Science and Technology,China(No.XTCX202404)。
文摘This study focused on improving the cathode performance of Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.15)O_(3-δ)(BSCN)-based perovskite materials through molybdenum(Mo)doping.Pure BSCN and Mo-modified-BSCN—Ea_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.1)Mo_(0.05)O_(3-δ)(B S CNM_(0.05)),Ba_(0.6)Sr_(0.4)Co_(0.85)Nb_(0.05)Mo_(0.1)O_(3-δ)(BSCNM_(0.1)),and Ba_(0.6)Sr_(0.4)Co_(0.85)Mo_(0.15)O_(3-δ)(BSCM)—with Mo doping contents of 5mol%,10mol%,and15mol%,respectively,were successfully prepared using the sol-gel method.The effects of Mo doping on the crystal structure,conductivity,thermal expansion coefficient,oxygen reduction reaction(ORR)activity,and electrochemical performance were systematically evaluated using X-ray diffraction analysis,thermally induced characterization,electrochemical impedance spectroscopy,and single-cell performance tests.The results revealed that Mo doping could improve the conductivity of the materials,suppress their thermal expansion effects,and significantly improve the electrochemical performance.Surface chemical state analysis using X-ray photoelectron spectroscopy revealed that 5mol%Mo doping could facilitate a high adsorbed oxygen concentration leading to enhanced ORR activity in the materials.Density functional theory calculations confirmed that Mo doping promoted the ORR activity in the materials.At an operating temperature of 600℃,the BSCNM_(0.05)cathode material exhibited significantly enhanced electrochemical impedance characteristics,with a reduced area specific resistance of 0.048Ω·cm~2,which was lower than that of the undoped BSCN matrix material by 32.39%.At the same operating temperature,an anode-supported single cell using a BSCNM_(0.05)cathode achieved a peak power density of 1477 mW·cm^(-2),which was 30.71%,56.30%,and 171.50%higher than those of BSCN,BSCNM_(0.1),and B SCM,respectively.The improved ORR activity and electrochemical performance of BSCNM_(0.05)indicate that it can be used as a cathode material in low-temperature solid oxide fuel cells.
文摘This paper discusses numerical methods for modelling cathodic protation (CP) using Boundary ElementMethods(BEM) for CP design analysis in comparision with the traditional methods and presentsseveral mathematical models (for CP design in 3-D infinite area) solvable by using BEM withmicrocomputer.
基金financially supported by the National Natural Science Foundation of China(No.41976036)the State Key Laboratory for Marine Corrosion and Protection,Luoyang Ship Material Research Institute(LSMRI)(Nos.KF190408 and KF190404)。
文摘A novel three-dimensional hierarchical WO_(3)photoelectrode was prepared by solvothermal method,and ZnO was deposited on its surface by electrochemical method.The WO_(3)/ZnWO_(4)/ZnO multiphaseheterojunction photoelectrode was prepared by further annealing treatment to explore the photoinduced cathodic protection(CP)performance.Compared with WO_(3)and ZnO,the photoinduced CP and electron storage capacity performance of WO_(3)/ZnWO_(4)/ZnO is significantly improved in 3.5%NaCl solution without adding any hole scavenger.The electron storage capacity of the WO_(3)/ZnWO_(4)/ZnO heterojunction makes it possible to continuously protect metallic materials in the dark after switching off the light,which can realize long-term and effective photoinduced CP.
文摘Metallic pipeline corrosion poses a significant challenge in the petrochemical industry. In this study, the design and control of a stand-alone photovoltaic (PV)-powered cathodic protection (CP) system based on the impressed current method were investigated. The proposed CP system was applied to a 250 km long steel-buried pipeline in the Sharm El-Sheikh region of Egypt. The system design involved the numerical modeling of the anode bed for the impressed current CP (ICCP) system and the sizing of the DC power source, including the PV array and battery bank. The system was designed and controlled to deliver a constant and continuous anode current to protect the underground pipeline from corrosion during daylight and nighttime. A maximum power point tracking (MPPT) algorithm based on the fractional open-circuit voltage (FOCV) technique was implemented to maximize power extraction from the PV array. Additionally, a proportional-integral (PI) controller was optimized and employed to achieve MPPT, while another PI controller managed the anode current of the CP system. Safe charging and discharging of the system’s battery are ensured via an ON-OFF controller. The parameters of the PI controllers were optimized using the particle swarm optimization (PSO) technique. Simulation results demonstrated that the proposed CP system achieved the required protection objectives successfully.
基金supported by the National Key Research and Development Program(No.2022YFC2806200)the National Key Research and Development Program(No.2023YFC2810800)the Natural Science Foundation of China(No.52001055).
文摘In this study,the pure erosion behaviour of pure iron and its erosion-corrosion behaviour under different anodic polarization currents were investigated in various cathodic reactions(oxygen reduction,hydrogen ion reduction,and water reduction)using a cylindrical stirring system.The corrosion-enhanced erosion(C-E)rates were determined for each condition.The results revealed that pure iron displayed similar pure erosion behaviour across all three cathodic reactions.When the cathodic reactions involve hydrogen ion reduction or water reduction,the erosion-corrosion of pure iron manifested as uniform damage,with the reduction in hardness being the main cause of the C-E in this case.Conversely,in the case of oxy-gen reduction reaction as the cathodic reaction,the erosion-corrosion presented as pitting damage,with the reduction in hardness resulting from localized concentration of anodic current and the formation of easily worn protruding flaky iron structures at the edges of the pits as the main mechanism of the C-E.Moreover,linear and exponential relationships were found between the C-E rate and the anodic current density for uniform damage and pitting damage,respectively.Finally,the concept of surface equivalent hardness was proposed,along with the establishment of a mathematical model for surface equivalent hardness based on the relationships between the C-E rate and the anodic current density.Utilizing the surface equivalent hardness enables the evaluation of the erosion rate on material surfaces considering the coupled effect.
文摘This work presents a study on the use of cathodic protection as a measure against corrosion in pipelines.The cathodic protection,compliant with the API 5L standard,is implemented here by applying an impressed current,while carefully considering several essential variables,such as soil characteristics,the type and color of the pipeline material,as well as the placement and size of the anode.Therefore,it is crucial to optimize the location and values of anodic overflows or ground resistances to ensure a uniform distribution of potential across the entire structure.In this method,impressed current protection uses an auxiliary anode and an external direct current source to induce a current through the electrolyte and the pipeline,thus countering the resistance of the steel.This approach is advantageous as it allows for the adjustment of electrical characteristics,particularly current levels,to meet specific needs.The factors essential to the effectiveness of cathodic protection systems,which optimize the distribution of protection potential across the structure,largely depend on the precise management of ground resistances during anodic discharge,particularly the attenuation coefficient(α).These factors were studied,and the results obtained were presented and discussed based on their influence.
基金supported by the Sichuan Science and Technology Program(No.2024NSFJQ0034)the National Natural Science Foundation of China(No.52271073)+1 种基金the Education and Teaching Reform Program for Graduate Students of Sichuan Province(No.YJGXM24-C047)the Innovation Team Funds of China West Normal University(No.KCXTD2024-1).
文摘A novel and long-lasting N_(3)BD/TiO_(2) composite photoanode with stable and superior photoelectrochemical and photoelectrochemical cathodic protection(PECCP)performances was achieved by synthesizing and depositing covalent organic framework(N_(3)BD)on titanium oxide(TiO_(2))nanotube arrays.The composite's increased visible light absorption capability enhanced the galvanic corrosion protection of nickel-phosphorus alloy-coated magnesium alloy(Mg/Ni)through PECCP technology.The open circuit potential(OCP)drops of the Mg/Ni electrode coupling with the N_(3)BD/TiO_(2) composite were 310 and 630 mV at dark state and under illumination,respectively.They remained relatively stable under intermittent visible light irradiation within 72 h,demonstrating excellent long-term stability.The superior photoelectrochemical and PECCP properties of the N_(3)BD/TiO_(2) are attributed to forming S-scheme heterojunctions,which effectively promote the separation and transfer of photogenerated electron-hole pairs and retain a strong redox capacity.This finding provides new insight into the design and synthesis of COF-modified photoanode with highly efficient and stable photoelectrochemical and PECCP performances.
基金support from the Nuclear Fuel Pellet Appearance Quality Inspection Device Project(20190304 A).
文摘Thefield of energy storage devices is primarily dominated by lithium-ion batteries(LIBs)due to their mature manufacturing processes and stable performance.However,immature lithium recovery technology cannot stop the continuous increase in the cost of LIBs.Along with the rapid development of electric transportation,it has become inevitable to trigger a new round of competition in alternative energy storage systems.Some monovalent rechargeable metal ion batteries(sodium ion batteries(SIBs)and potassium ion batteries(PIBs),etc.)and multi-valent rechargeable metal-ion batteries(magnesium ion batteries(MIBs),calcium ion batteries(CIBs),zinc ion batteries(ZIBs),and aluminum ion batteries(AIBs),etc.)are potential candidates,which can replace LIBs in some of the scenarios to alleviate the pressure on supply.The cathode material plays a crucial role in determining the battery capacity.Transition metal compounds dominated by layered transition metal oxides as key cathode materials for secondary batteries play an important role in the advancement of various battery energy storage systems.In summary,this manuscript aims to review and summarize the research progress on transition metal compounds used as cathodes in different metal ion batteries,with the aim of providing valuable guidance for the exploration and design of high-performance integrated battery systems.
基金financially supported by the Henan Province Key R&D and Promotion Project(Technology Research)(NO.232102230011)the Fundamental Research Fund of Henan Academy of Sciences(NO.230618026)+1 种基金Joint Fund of Henan Province Science and Technology R&D Program(NO.225200810120)High-level Talent Research Start-up Project Funding of Henan Academy of Sciences(NOs.231818022 and 232018001).
文摘Constructing a photoanode with both high dark-state protection performance and high stability remains a top priority for photoelectrochemical cathodic protection technology,especially in a marine environment(dark-state or rainy conditions)without hole scavenging agents.In this work,we developed a class of energy-storage quasi-planar heterojunctions(WO_(3)-Nb_(2)O_(5)-ZnIn_(2)S_(4))with directional paths(low onset potential and well-matched energy band)and embedded morphology.The co-design of embedded and directional paths reduces the carrier transport energy barrier at the composite interface,and increases the interface contact area,thereby achieving highly stable and sensitive dark-state energy storage and photoelectrochemical cathodic protection performance in 3.5 wt.%NaCl solution without hole scavenging agent(Dark-state energy storage efficiency increased by 43%.For carbon steel,the performance retention rate is 99.6%after 500 cycles,the performance retention rate is 89%after 5000 s).
基金support by the Department of Science&Technology of Zhejiang Province under grant no.2024C01095Zhejiang Provincial Natural Science Foundation of China under grant nos.LD22E020006 and LBMHD24E020001the National Natural Science Foundation of China(NSFC)under grant nos.21972127,U20A20253,and 22279116.
文摘Coupling with high-voltage oxide cathode is the key to achieve high-energy density sulfide-based all-solid-state lithium batteries.However,the complex interfacial issues including the space charge layer effect and undesirable side reaction between sulfide solid-state electrolytes and oxide cathode materials are the main constraints on the development of high-performance allsolid-state lithium batteries,which lead to the continuous decay of electrochemical performance.Herein,different from the complicated coating procedure,a LiPO_(2)F_(2)additive engineering was proposed to achieve high-performance all-solid-state lithium batteries.With the introduction of LiPO_(2)F_(2)additive,a protective cathode-electrolyte interphase consisting of LiPxOyFz,LiF,and Li_(3)PO_(4)could be in situ formed to improve the interfacial stability between LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)and Li_(5.5)PS_(4.5)Cl_(1.5)(LPSC).Benefiting from this,the NCM811/LPSC/Li all-solid-state lithium battery exhibited impressive cyclic stability with a capacity retention of 85.5%after 600 cycles(at 0.5 C).Diverse and comprehensive characterization,combined with finite element simulation and density functional theory calculation fully demonstrated the effective component,interfacial stabilization function and enhanced kinetic of LiPO_(2)F_(2)-derived cathode-electrolyte interphase.This work provides not only a feasible and effective method to stabilize the cathodic interface but also worthy insight into interfacial design for high-performance all-solid-state lithium batteries.
基金financially supported by the National Natural Science Foundation of China(Grant No.52402215)the Anhui Provincial Natural Science Foundation(2408085QB036)+1 种基金the Natural Science Research Project of Anhui Province Education Department(Grant Nos.2022AH050334,2022AH030046,2023AH051119)the Scientific Research Foundation of Anhui University of Technology for Talent Introduction(DT2200001211)。
文摘Sodium-ion batteries are the prominent device for stationary energy storage system and low-speed electric vehicles.However,the practical application is still limited by the unsatisfied performance and high cost of the cathode side,which strictly requires the development of high voltage,high capacity,and earth-abundant cathode material.Ni-Fe-Mn ternary layered oxide has been recognized as one of the most promising standard type of cathodes.However,the composition and phase structure on high-voltage characteristics have not been well investigated.Herein,selecting the typically high-voltage cathode of P2-Na_(0.67)Ni_(0.33)Mn_(0.67)O_(2)as a parent material,we fabricate ten Ni-Fe-Mn ternary layered oxides through replacing the Ni,Mn,or both Ni and Mn by Fe.The thermodynamically stable phase diagram for those materials is presented.The electrochemical properties for all the samples are investigated in detail.Three potential Ni-Fe-Mn ternary layered oxides are picked up considering the energy density,cycle stability,kinetics,cost price,and working voltage,which demonstrate great potential for surpassing the performance of lithium iron phosphate.The related electrochemical reaction and fading mechanism are well revealed.This work provides some new foundational Ni-Fe-Mn ternary layered materials for high-voltage sodium-ion batteries.
基金financially supported by the Natural Science Foundation of Shandong(No.ZR2023QD152)the National Natural Science Foundation of China(No.42476212).
文摘Photogenerated electrons generated by photoexcitation of semiconductor materials can be transferred to metal materials to provide corrosion protection.Conversely,the accumulation of photogenerated holes accelerates the recombination of photogenerated carriers.Consequently,the development of efficient strategies for the consumption of photogenerated holes has emerged as a critical challenge in the field of photoelectrochemical cathodic protection technology.In this paper,TiO_(2)/TiOBr heterojunction photoelectrode was firstly prepared by simple hydrothermal method,and NiCo-LDH(layered double hydroxide)was further deposited on TiO_(2)/TiOBr to obtain TiO_(2)/TiOBr/NiCo-LDH photoelectrode.The construction of a heterojunction between TiO_(2)and TiOBr promotes the separation of photogenerated carriers,while the deposition of NiCo-LDH reduces the overpotential for hole oxidation.Hence,the photoinduced potential drop and photoinduced current density of TiO_(2)/TiOBr/NiCo-LDH photoelectrode coupled with 316 L stainless steel in 3.5 wt%NaCl under simulated sunlight irradiation can be up to 303 mV and 25.87μA/cm^(2),respectively.This study provides a new idea for the design and preparation of TiO_(2)-based photoelectrodes with excellent photocathodic protection under visible light.
基金financially supported by the National Natural Science Foundation of China(Nos.22272118,22172111 and 22309134)the Science and Technology Commission of Shanghai Municipality,China(Nos.22ZR1464100,20ZR1460300 and 19DZ2271500)+3 种基金China Postdoctoral Science Foundation(2022M712402)Shanghai Rising-Star Program(23YF1449200)Zhejiang Provincial Science and Technology Project(2022C01182)the Fundamental Research Funds for the Central Universities(22120210529 and 2023-3-YB-07)。
文摘Compared with Zn^(2+),the current mainly reported charge carrier for zinc hybrid capacitors,small-hydrated-sized and light-weight NH_(4)^(+)is expected as a better one to mediate cathodic interfacial electrochemical behaviors,yet has not been unraveled.Here we propose an NH_(4)^(+)-modulated cationic solvation strategy to optimize cathodic spatial charge distribution and achieve dynamic Zn^(2+)/NH_(4)^(+)co-storage for boosting Zinc hybrid capacitors.Owing to the hierarchical cationic solvated structure in hybrid Zn(CF_(3)SO_(3))_(2)–NH_4CF_(3)SO_(3)electrolyte,high-reactive Zn^(2+)and small-hydrate-sized NH_4(H_(2)O))(4)^(+)induce cathodic interfacial Helmholtz plane reconfiguration,thus effectively enhancing the spatial charge density to activate 20%capacity enhancement.Furthermore,cathodic interfacial adsorbed hydrated NH_(4)^(+)ions afford high-kinetics and ultrastable C···H(NH_(4)^(+))charge storage process due to a much lower desolvation energy barrier compared with heavy and rigid Zn(H_(2)O)_6^(2+)(5.81 vs.14.90 eV).Consequently,physical uptake and multielectron redox of Zn^(2+)/NH_(4)^(+)in carbon cathode enable the zinc capacitor to deliver high capacity(240 mAh g^(-1)at 0.5 A g^(-1)),large-current tolerance(130 mAh g^(-1)at 50 A g^(-1))and ultralong lifespan(400,000cycles).This study gives new insights into the design of cathode–electrolyte interfaces toward advanced zinc-based energy storage.
文摘Correction to:Nano-Micro Letters(2025)17:117 https://doi.org/10.1007/s40820-025-01660-0 Following publication of the original article[1],the authors reported that the supplementary file needed to be updated because they mistakenly used the incorrect version.The original article[1]has been corrected.
文摘The effect of 10% Si （mole fraction） addition on TiAlSiN coatings was studied. Ti0.5Al0.5N, Ti0.5Al0.4Si0.1N and Ti0.55Al0.35Si0.1N coatings were deposited on WC？Co substrates by cathodic arc evaporation. The microstructure and mechanical properties were characterized by X-ray diffraction （XRD）, X-ray photoelectron spectroscopy （XPS）, scanning electron microscopy （SEM）, nano-indentation measurement and scratch test. The mechanisms of how Si affects the properties and failure modes of TiAlSiN coatings were also discussed. The results show that the addition of 10% Si results in the formation of nc-（Ti,Al,Si）N/a-Si3N4 nano-composite structure. The hardness and toughness of TiAlSiN coatings increase, whereas the coating adhesion strength decreases. Compared with Ti0.55Al0.35Si0.1N coating, Ti0.5Al0.4Si0.1N coating has higher hardness but lower toughness. The dominant failure mode of TiAlN coating is wedging spallation due to low toughness and strong interfacial adhesion. The dominant failure mode of TiAlSiN coatings is buckling spallation due to improved toughness and weakened interfacial adhesion.
文摘A novel type of composite electrode based on nmltiwalled carbon nanotubes coated with sheet-like cobalt hydroxide particles was used in supercapacitors. Cobalt hydroxide cathodlcally deposited fiom Co（NO3）O2 solution with carbon nanotubes as matrix exhibited large pseudo-capacitance of 322 F/g in 1 mol/L KOH. To characterize the cobalt hydroxide nanocomposite electrode, a charge-discharge cycling test, cyclic voltammetry, and an impedance test were done. This cobalt hydroxide composite exhibiting excellent pseudo-capacitive behavior （i.c. high reversibility, high specific capacitance, low impedance）, was demonstrated to be a candidate for the application of electrochemical supercapacitors. A combined capacitor consisting of cobalt hydroxide composite as a cathode and activated carbon fiber as an anode was reported. The electrochemical pcrformance of the combined capacitor was characterized by cyclic voltammetry and a dc charge/discharge test. The combined capacitor showed ideal capacitor behavior with an extended operating voltage of 1.4 V. According to the extended operating voltage, the energy density of the combined capacitor at a current density of 100 mA/cm^2 was found to be 11 Wh/kg. The combined capacitor exhibited high-energy density and stable power characteristics,
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korea government(MSIT)(No.2022M3H4A6A0103720142)the National Research Council of Science&Technology(NST)grant by the Korea government(MSIT)(No.GTL24011-000)+1 种基金the Technology Innovation Program(RS-2024-00404165)through the Korea Planning&Evaluation Institute of Industrial Technology(KEIT)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea)supported by the Samsung SDI Co.Ltd.and the Korea Institute of Science and Technology(KIST)institutional program(2E33942,2E3394B)。
文摘Strategies for achieving high-energy-density lithium-ion batteries include using high-capacity materials such as high-nickel NCM,increasing the active material content in the electrode by utilizing high-conductivity carbon nanotubes(CNT)conductive materials,and electrode thickening.However,these methods are still limited due to the limitation in the capacity of high-nickel NCM,aggregation of CNT conductive materials,and nonuniform material distribution of thick-film electrodes,which ultimately damage the mechanical and electrical integrity of the electrode,leading to a decrease in electrochemical performance.Here,we present an integrated binder-CNT composite dispersion solution to realize a high-solids-content(>77 wt%)slurry for high-mass-loading electrodes and to mitigate the migration of binder and conductive additives.Indeed,the approach reduces solvent usage by approximately 30%and ensures uniform conductive additive-binder domain distribution during electrode manufacturing,resulting in improved coating quality and adhesive strength for high-mass-loading electrodes(>12 mAh cm^(−2)).In terms of various electrode properties,the presented electrode showed low resistance and excellent electrochemical properties despite the low CNT contents of 0.6 wt%compared to the pristine-applied electrode with 0.85 wt%CNT contents.Moreover,our strategy enables faster drying,which increases the coating speed,thereby offering potential energy savings and supporting carbon neutrality in wet-based electrode manufacturing processes.
基金supported by the National Natural Science Foundation of China(Nos.U2341209 and 52130407).
文摘A novel trace nickel(Ni)doped tungsten(W)matrix with coated Ni on W grains was prepared by powder metallurgy method.The introduction of Ni can inhibit the reaction between W and barium-calcium aluminates(Ba-Ca aluminates)during the impregnation process of the matrix.After cathode activation,the surface Ba:O molar ratio is 0.88:1.00,much higher than the Ba dispenser cathode without Ni doping.The XPS results of the cathode surface showed that the metallic Ba appeared on the activated cathode surface,forming dipoles with oxygen,and effectively reducing the cathode surface work function.The pulse electron emission current density at 1100℃_(b)(brightness temperature)was 18.26 A/cm^(2),and the calculated work function was 1.97 eV.It has a low evaporation rate and the accelerated lifetime test predict a lifetime of over 160000 h.First-principles calculations showed that the charge transfer and dipole moment in the NiW-BaO system were both increased compared to the Ba dispenser cathode,thus improving the emission performance of the Ni-W mixed matrix cathode.
基金We would like to show gratitude to the Yunnan Province Basic Research Major Project(202501BC070006(Y.Wang))Key Industry Science and Technology Projects for University Services in Yunnan Province(FWCY ZNT2024002(Y.Wang))+3 种基金National Natural Science Foundation of China(22279070(L.Wang))and(U21A20170(X.He))the Ministry of Science and Technology of China(2019YFA0705703(L.Wang))Beijing Natural Science Foundation(L242005(X.He))Key Industry Science and Technology Projects for University Services in Yunnan Province(FWCY BSPY2024011(T.Lai)).
文摘Long-life energy storage batteries are integral to energy storage systems and electric vehicles,with lithium-ion batteries(LIBs)currently being the preferred option for extended usage-life energy storage.To further extend the life span of LIBs,it is essential to intensify investments in battery design,manufacturing processes,and the advancement of ancillary materials.The pursuit of long durability introduces new challenges for battery energy density.The advent of electrode material offers effective support in enhancing the battery’s long-duration performance.Often underestimated as part of the cathode composition,the binder plays a pivotal role in the longevity and electrochemical performance of the electrode.Maintaining the mechanical integrity of the electrode through judicious binder design is a fundamental requirement for achieving consistent long-life cycles and high energy density.This paper primarily concentrates on the commonly employed cathode systems in lithium-ion batteries,elucidates the significance of binders for both,discusses the application status,strengths,and weaknesses of novel binders,and ultimately puts forth corresponding optimization strategies.It underscores the critical function of binders in enhancing battery performance and advancing the sustainable development of lithium-ion batteries,aiming to offer fresh insights and perspectives for the design of high-performance LIBs.
基金supported by the financial support from the National Research Foundation,Singapore,under its Singapore-China Joint Flagship Project(Clean Energy).
文摘Aqueous Zn-iodine batteries(ZIBs)face the formidable challenges towards practical implementation,including metal corrosion and rampant dendrite growth on the Zn anode side,and shuttle effect of polyiodide species from the cathode side.These challenges lead to poor cycle stability and severe self-discharge.From the fabrication and cost point of view,it is technologically more viable to deploy electrolyte engineering than electrode protection strategies.More importantly,a synchronous method for modulation of both cathode and anode is pivotal,which has been often neglected in prior studies.In this work,cationic poly(allylamine hydrochloride)(Pah^(+))is adopted as a low-cost dual-function electrolyte additive for ZIBs.We elaborate the synchronous effect by Pah^(+)in stabilizing Zn anode and immobilizing polyiodide anions.The fabricated Zn-iodine coin cell with Pah^(+)(ZnI_(2) loading:25 mg cm^(−2))stably cycles 1000 times at 1 C,and a single-layered 3.4 cm^(2) pouch cell(N/P ratio~1.5)with the same mass loading cycles over 300 times with insignificant capacity decay.
