Na_(3)V_(2)(PO_(4))_(2)O_(2)F (VP) is recognized as a promising cathode material for sodium-ion batteries due to its stable structural framework and high specific capacity.Density functional theory (DFT) and finite el...Na_(3)V_(2)(PO_(4))_(2)O_(2)F (VP) is recognized as a promising cathode material for sodium-ion batteries due to its stable structural framework and high specific capacity.Density functional theory (DFT) and finite element simulations show that incorporating SO_(4)^(2-)into VP decreases its band gap,lowers the migration energy barrier,and ensures a uniform Na+concentration gradient and stress distribution during charge and discharge cycles.Consequently,the average Na+diffusion coefficient of Na_(3)V_(2)(PO_(4))_(1.95)(SO_(4))_(0.05)O_(2)F(VPS-1) is roughly double that of VP,leading to enhanced rate capability (80 C,75.5 mAh g^(-1)) and cycling stability (111.0 mAh g^(-1)capacity after 1000 cycles at 10 C current density) for VPS-1.VPS-1 exhibits outstanding fast-charging capabilities,achieving an 80%state of charge in just 8.1 min.The assembled VPS-1//SbSn/NPC full cell demonstrated stable cycling over 200 cycles at a high 5 C current,maintaining an average coulombic efficiency of 95.35%.展开更多
Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-stat...Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-state lithium batteries(ASSLBs)compared to the overly reactive metallic lithium anode and the mechanically weak silicon anode.This study finds that the pre-lithiated Al anode demonstrates outstanding interfacial stability with the Li_6PS_5Cl(LPSCl)electrolyte,maintaining stable cycling for over 1200 h under conditions of deep charge-discharge.This paper combines the pre-lithiated Al anode with a high-nickel cathode,LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2),paired with the highly ionic conductive LPSCl electrolyte,to design an ASSLB with high energy density and stability.Using anode pre-lithiation techniques,along with dual-reinforcement technology between the electrolyte and the cathode active material,the ASSLB achieves stable cycling for 1000 cycles at a 0.2C rate,with a capacity retention rate of up to 82.2%.At a critical negative-to-positive ratio of 1.1,the battery's specific energy reaches up to 375 Wh kg^(-1),and it maintains over 85.9%of its capacity after 100 charge-discharge cycles.This work provides a new approach and an excellent solution for developing low-cost,high-stability all-solid-state batteries.展开更多
Flat-panel X-ray sources(FPXSs)have many advantages in terms of compactness and low-dose imaging,enhancing their capability for novel X-ray applications.Experimental analysis of the X-ray characteristics and optimizin...Flat-panel X-ray sources(FPXSs)have many advantages in terms of compactness and low-dose imaging,enhancing their capability for novel X-ray applications.Experimental analysis of the X-ray characteristics and optimizing the anode panel of an FPXS are time-consuming,expensive,and sometimes impractical.In this study,a FPXS was prepared using a ZnO nanowire cold cathode and a molybdenum film anode target.Monte Carlo(MC)simulations were utilized to optimize the anode panel and obtain the average fluence,average energy,and spatial distribution of the X-rays for the ZnO nanowire FPXS.The accuracy of the MC simulations was verified by comparing the measured and simulated energy spectra.Optimization of the anode target considers the material,thickness,and morphology,whereas optimization of the substrate focuses on the material and thickness.The results show that the difference between the positions of the K-shell peaks in the measured and simulated energy spectra is within 0.26 keV.At the acceleration voltages of 30 kV,60 kV,and 90 kV,the optimal thicknesses of the tungsten array anode were 0.65μm,2.45μm,and 5μm,respectively,while the molybdenum array anode has the optimal thicknesses of 1.45μm,5.25μm,and 24μm,respectively.The microsemi-ellipsoidal anode with a recessed design showed a 5%increase in the transmitted X-ray fluence compared with the film target.The sapphire substrate with a thickness of 0.78 mm exhibits a mechanical strength comparable to that of a glass substrate with a thickness of 3 mm,implying that the former can increase the average X-ray fluence by reducing the filtration of X-rays.The findings of this study provide valuable guidance for the fabrication and optimization of the ZnO nanowire FPXS.展开更多
Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphi...Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphite.This study utilizes the porous“defect advantage”of a cathode carbon block matrix to prepare silicon-doped and asphalt-coated detoxified and purified waste graphitization cathode carbon blocks for use as high-performance silicon/carbon composite anode materials.The results show that the uniformly silicondoped silicon/carbon composite material features a unique amorphous carbon-encapsulated“locked silicon”structure,which effectively addresses issues such as cathode volume expansion,excessive growth of the solid electrolyte interphase(SEI)film,and poor electrical contact between active materials.Consequently,electrochemical performance is enhanced.After assembly in a half-cell,the PSCC/10%Si@C(purified waste graphitization cathode carbon/10%Si@C)material exhibits optimal electrochemical stability,with an initial charging specific capacity of 514.5 mAh/g at 0.1 C(1 C=170 mA/g)and a capacity retention rate of 95.1%after 100 cycles.At a charge rate of 2.0 C,a specific capacity of 216.9 mAh/g is achieved.This technology provides a new pathway for the economical and high-value utilization of waste cathode carbon blocks and the development of low-cost,high-performance anode materials.展开更多
Flow anodic oxidation system has demonstrated to be a promising and environmental benign water treatment technology because of its advantages of high contaminant removal efficiency and low energy consumption.However,t...Flow anodic oxidation system has demonstrated to be a promising and environmental benign water treatment technology because of its advantages of high contaminant removal efficiency and low energy consumption.However,traditional setup needs an external unit for flow anode material separation and recovery,which inevitably increases the capital cost and hinders its continuous operation.Herein,a specific porous cathode is introduced to achieve continuous water purification with high contaminant removal in a flow anodic oxidation system.The efuent concentration of carbamazepine(CBZ),a common and model contaminant widely detected in natural water environment,was reduced by 99%.The linear sweep voltammetry(LSV)and quenching tests demonstrated that HO·was the dominant reactive species.While the removal of contaminants was inhibited in practical surface water,largely related to the quenching by dissolved organic matter and bicarbonate,the flow anodic oxidation process was competent in alleviating the ecotoxicity following oxidation.Our study constructs a modular device for cost-effective continuous water purification and provides insight into the mechanisms of flow andic oxidation.展开更多
Binders could play crucial or even decisive roles in the fabrication of low-cost, stable and high-capacity electrodes. This is especially the case for the silicon (Si) anodes and sulfur (S) cathodes that undergo large...Binders could play crucial or even decisive roles in the fabrication of low-cost, stable and high-capacity electrodes. This is especially the case for the silicon (Si) anodes and sulfur (S) cathodes that undergo large volume change and active material loss in lithium-ion batteries during prolonged cycles. Herein, a hydrophilic polymer poly(methyl vinyl ether-alt-maleic acid) (PMVEMA) was explored as a dual-functional aqueous binder for the preparation of high-performance silicon anode and sulfur cathode. Benefiting from the dual functions of PMVEMA, i.e., the excellent dispersion ability and strong binding forces, the as-prepared electrodes exhibit improved capacity, rate capability and long-term cycling performance. In particular, the as-prepared Si electrode delivers a high initial discharge capacity of 1346.5 mAh g^(−1) at a high rate of 8.4 A/g and maintains 834.5 mAh g^(−1) after 300 cycles at 4.2 A/g, while the as-prepared S cathode exhibits enhanced cycling performance with high remaining discharge capacities of 663.4 mAh g^(−1) after 100 cycles at 0.2 C and 487.07 mAh g^(−1) after 300 cycles at 1 C, respectively. These encouraging results suggest that PMVEMA could be a universal binder to facilitate the green manufacture of both anode and cathode for high-capacity energy storage systems.展开更多
To control the power hierarchy design of lithium-ion battery(LIB)builtup sets for electric vehicles(EVs),we offer intensive theoretical and experimental sets of choice anode/cathode architectonics that can be modulate...To control the power hierarchy design of lithium-ion battery(LIB)builtup sets for electric vehicles(EVs),we offer intensive theoretical and experimental sets of choice anode/cathode architectonics that can be modulated in full-scale LIB built-up models.As primary structural tectonics,heterogeneous composite superstructures of full-cell-LIB(anode//cathode)electrodes were designed in closely packed flower agave rosettes TiO2@C(FRTO@C anode)and vertical-star-tower LiFePO4@C(VST@C cathode)building blocks to regulate the electron/ion movement in the three-dimensional axes and orientation pathways.The superpower hierarchy surfaces and multi-directional orientation components may create isosurface potential electrodes with mobile electron movements,in-to-out interplay electron dominances,and electron/charge cloud distributions.This study is the first to evaluate the hotkeys of choice anode/cathode architectonics to assemble different LIB-electrode platforms with high-mobility electron/ion flows and high-performance capacity functionalities.Density functional theory calculation revealed that the FRTO@C anode and VST-(i)@C cathode architectonics are a superior choice for the configuration of full-scale LIB built-up models.The integrated FRTO@C//VST-(i)@C full-scale LIB retains a huge discharge capacity(~94.2%),an average Coulombic efficiency of 99.85%after 2000 cycles at 1 C,and a high energy density of 127 Wh kg?1,thereby satisfying scale-up commercial EV requirements.展开更多
Sodium-ion batteries(SIBs) have gained more scientists’ interest, owing to some facts such as the natural abundance of Na, the similarities of physicochemical characteristics between Li and Na. The irreversible Na+io...Sodium-ion batteries(SIBs) have gained more scientists’ interest, owing to some facts such as the natural abundance of Na, the similarities of physicochemical characteristics between Li and Na. The irreversible Na+ions consumption during the first cycle of charge/discharge process(due to the formation of the solid electrolyte interface(SEI) on the electrode surface and other irreversible reactions) is the factor that determines high performance SIBs and largely reduces the capacity of the full cell SIBs. Thus, the initial coulombic efficiency(ICE) of SIBs for both anode and cathode materials, is a key parameter for high performance SIBs, and the point is to increase the transport rate of the Na+ions. Therefore, developing SIBs with high ICE and rate performance becomes vital to boost the commercialization of SIBs. Here we provide a review on the methods to improve the ICE and the rate performance, by summarizing some methods of improving the ICE and rate performance of the anode and cathode materials for SIBs, and end by a conclusion with some perspectives and recommendations.展开更多
Metal anodes based on plating/stripping electrochemistry,for instance,common alkaline metal lithium(Li),sodium(Na),potassium(K),polyvalent metal magnesium(Mg),aluminum(Al),calcium(Ca)and zinc(Zn)are imminently evoked ...Metal anodes based on plating/stripping electrochemistry,for instance,common alkaline metal lithium(Li),sodium(Na),potassium(K),polyvalent metal magnesium(Mg),aluminum(Al),calcium(Ca)and zinc(Zn)are imminently evoked and increasingly researched for future generation high-energy-density rechargeable batteries due to their large theoretical capacity,low electrochemical potential,and superior electronic conductivity in recent years.However,the uncontrolled dendrite formation issue induces low Coulombic efficiency,short lifespan,and hazardous security risks,hindering the actual applications of metal batteries.Among various solutions,the utilization of ferro-/piezoelectric materials for metal anodes displays active effects on decreasing local current density,suppressing dendrite growth,and tolerating volume expansion benefits from the unique ferro-/piezoelectric polarization effect.This review presents the research progress of ferro-/piezoelectric polarization effect for regulating the dendritic growth of metal anodes for the first time.First,the current challenges and strategies of metal anodes are proposed.Then,ferro-/piezoelectric materials and their working principle are discussed.Finally,the recent research progress of ferroelectric and piezoelectric materials on dynamic regulation of dendrite growth is summarized,and the future perspectives are prospected.We hope this review could draw more attention in designing metal anodes with self-polarization materials and promoting their practical applications.展开更多
This work presents a method to solve the weak solubility of zinc chloride(ZnCl_2) in the ethanol by adding some reasonable water into an ethanol electrolyte containing ZnCl_2 and myristic acid(CH_3(CH_2)_(12)COOH).A r...This work presents a method to solve the weak solubility of zinc chloride(ZnCl_2) in the ethanol by adding some reasonable water into an ethanol electrolyte containing ZnCl_2 and myristic acid(CH_3(CH_2)_(12)COOH).A rapid one-step electrodeposition process was developed to fabricate anodic(2.5 min) and cathodic(40 s) superhydrophobic surfaces of copper substrate(contact angle more than 150°) in an aqueous ethanol electrolyte.Morphology,composition,chemical structure and superhydrophobicity of these superhydrophobic surfaces were investigated by SEM,FTIR,XRD,and contact angle measurement,respectively.The results indicate that water ratio of the electrolyte can reduce the required deposition time,superhydrophobic surface needs over 30 min with anhydrous electrolyte,while it needs only 2.5 min with electrolyte including 10 mL water,and the maximum contact angle of anodic surface is 166° and that of the cathodic surface is 168°.Two copper electrode surfaces have different reactions in the process of electrodeposition time,and the anodic copper surface covers copper myristate(Cu[CH_3(CH_2)_(12)COO]_2) and cupric chloride(CuCl);while,zinc myristate(Zn[CH_3(CH_2)_(12)COO]_2) and pure zinc(Zn) appear on the cathodic surface.展开更多
Poly(ethylene oxide)(PEO)-based solid polymer electrolyte is always the most promising candidate for preparing thinner, lighter and safer lithium-ion batteries. However, the lithium dendrites growth of lithium anode a...Poly(ethylene oxide)(PEO)-based solid polymer electrolyte is always the most promising candidate for preparing thinner, lighter and safer lithium-ion batteries. However, the lithium dendrites growth of lithium anode and the high-voltage oxidation of cathode are easy to cause the PEO-based battery failure.The way to deal with the different challenges on both sides of the anode and cathode is pursued all the time. In this study, we reported a new strategy to construct the PVDF/PEO/PVDF three-layer structure for solid polymer electrolyte(marked as PVDF@PEO) using PVDF as the functional “skin”. The PVDF@PEO electrolyte can effectively prevent from the lithium dendrites, and shows a stable cycling life over1000 h in the Li/PVDF@PEO/Li cell. In addition, the PVDF@PEO electrolyte exhibits higher oxidation resistance and can be matched with high-voltage LiCoO_(2) cathode. The Li/PVDF@PEO/LiCoO_(2) cell delivered a specific capacity of about 150 m Ah g^(-1) over 150 cycles and maintained good cycling stability. Our research provides insights that the polymer electrolytes constructed with PVDF functional “skin” can simultaneously meet the challenges of both anode and cathode in solid-state lithium-ion batteries(SSLIBs).展开更多
Dual ion batteries(DIBs) exhibit broad application prospects in the field of electrical energy storage(EES)devices with excellent properties,such as high voltage,high energy density,and low cost.In the graphitebased D...Dual ion batteries(DIBs) exhibit broad application prospects in the field of electrical energy storage(EES)devices with excellent properties,such as high voltage,high energy density,and low cost.In the graphitebased DIBs,high voltage is needed to store enough anions with the formation of anion intercalation compound XCn(X=AlCl4-,PF6-,TFSI-,etc.).Hence,it is difficult for graphite-based DIBs to match proper anodes and electrolytes.Here,an Se/graphene composite is prepared via a convenient method,and assembled into a dual-ion full battery(DIFB) as anode with graphite cathode and 1 mol/L NaPF6 in EC:EMC(1:1,v:v).This DIFB has achieved a high discharge capacity of 75.9 mAh/g and high medium output voltage of 3.5 V at 0.1 A/g.Actually,the suitable anode materials,such as the present Se/graphene composite,are extremely important for the development and application of graphite-based DIBs.This study is enlightening for the design of future low-cost EES devices including graphite-based DIBs.展开更多
In this paper, the effects of zinc （Zn） and magnesium （Mg） addition on the performance of an aluminum-based sacrificial anode in seawater were investigated using a potential measurement method. Anodic efficiency, ...In this paper, the effects of zinc （Zn） and magnesium （Mg） addition on the performance of an aluminum-based sacrificial anode in seawater were investigated using a potential measurement method. Anodic efficiency, protection efficiency, and polarized potential were the parameters used. The percentages of Zn and Mg in the anodes were varied from 2% to 8% Zn and 1% to 4% Mg. The alloys produced were tested as sacrificial anodes for the protection of mild steel in seawater at room temperature. Current efficiency as high as 88.36% was obtained in alloys containing 6% Zn and 1% Mg. The polarization potentials obtained for the coupled （steel/Al-based alloys） are as given in the Pourbaix diagrams, with steel lying within the immunity region/cathodic region and the sacrificial anodes within the anodic region. The protection offered by the sacrificial anodes to the steel after the 7th and 8th week was measured and protection efficiency values as high as 99.66% and 99.47% were achieved for the A1-6%Zn-l%Mg cast anode. The microstructures of the cast anodes comprise of intermetallic structures of hexagonal Mg3Zn2 and body-centered cubic A12Mg3Zn3. These are probably responsible for the breakdown of the passive alumina film, thus enhancing the anode efficiency.展开更多
The energy density of commercial lithium(Li)ion batteries with graphite anode is reaching the limit.It is believed that directly utilizing Li metal as anode without a host could enhance the battery’s energy density t...The energy density of commercial lithium(Li)ion batteries with graphite anode is reaching the limit.It is believed that directly utilizing Li metal as anode without a host could enhance the battery’s energy density to the maximum extent.However,the poor reversibility and infinite volume change of Li metal hinder the realistic implementation of Li metal in battery community.Herein,a commercially viable hybrid Li-ion/metal battery is realized by a coordinated strategy of symbiotic anode and prelithiated cathode.To be specific,a scalable template-removal method is developed to fabricate the porous graphite layer(PGL),which acts as a symbiotic host for Li ion intercalation and subsequent Li metal deposition due to the enhanced lithiophilicity and sufficient ion-conducting pathways.A continuous dissolution-deintercalation mechanism during delithiation process further ensures the elimination of dead Li.As a result,when the excess plating Li reaches 30%,the PGL could deliver an ultrahigh average Coulombic efficiency of 99.5% for 180 cycles with a capacity of 2.48 m Ah cm^(-2) in traditional carbonate electrolyte.Meanwhile,an air-stable recrystallized lithium oxalate with high specific capacity(514.3 m Ah g^(-1))and moderate operating potential(4.7-5.0 V)is introduced as a sacrificial cathode to compensate the initial loss and provide Li source for subsequent cycles.Based on the prelithiated cathode and initial Li-free symbiotic anode,under a practical-level3 m Ah capacity,the assembled hybrid Li-ion/metal full cell with a P/N ratio(capacity ratio of Li Ni_(0.8)Co_(0.1)Mn_(0.1)O_(2) to graphite)of 1.3exhibits significantly improved capacity retention after 300 cycles,indicating its great potential for high-energy-density Li batteries.展开更多
Vacuum space between Ar atoms in unlighted HCFL lamps is an electric insulator, because vacuum fills up with strong negative electric field from orbital electrons in 3p6 electron shell of Ar atoms. Vacuum space in lig...Vacuum space between Ar atoms in unlighted HCFL lamps is an electric insulator, because vacuum fills up with strong negative electric field from orbital electrons in 3p6 electron shell of Ar atoms. Vacuum space in lighted FL lamps changes to the neutral vacuum that provides a superconductive vacuum for moving electrons at above room temperature. The complications of lighting mechanisms of HCFL lamps for more than 80 years have clearly solved with coexistence of disparate external and internal electric circuits for each half cycle. External electric circuit acts as two roles. One helps for formation of internal electric circuit in Ar gas space by electric field. Other picks up induced voltages from capacitor CFL. HCFL lamp only lights up with moving electrons in internal DC driving circuit. Electrons in HCFL lamp only move from cathode to anode, which respectively have negative and positive potentials against grand (V = 0), and which are formed with volumes of heated corona light (4G) at around W-filament metal electrodes with a help of heated BaO particles. The HCFL lamp that emits thermoelectrons is a false story. Here we have totally revised the fundamentals of the lighting mechanism of the established HCFL lamps for last 80 years.展开更多
Experimental investigations and associated methods are provided to characterize the mechanical properties of a lithium-ion battery accounting for operating temperature variation and thermal effects. Material propertie...Experimental investigations and associated methods are provided to characterize the mechanical properties of a lithium-ion battery accounting for operating temperature variation and thermal effects. Material properties for LiFeP04 cathode and anode samples taken from an off-the-shelf battery are evaluated in new and fatigued （subjec- ted to charging and discharging cycles） conditions.展开更多
Current aqueous battery electrolytes,including conve ntional hydrogel electrolytes,exhibit unsatisfactory water retention capabilities.The sustained water loss will lead to subsequent polarization and increased intern...Current aqueous battery electrolytes,including conve ntional hydrogel electrolytes,exhibit unsatisfactory water retention capabilities.The sustained water loss will lead to subsequent polarization and increased internal resistance,ultimately resulting in battery failure.Herein,a double network(DN) orga no hydrogel electrolyte based on dimethyl sulfoxide(DMSO)/H_(2)O binary solvent was proposed.Through directionally reconstructing hydrogen bonds and reducing active H_(2)O molecules,the water retention ability and cathode/anode interfaces were synergistic enhanced.As a result,the synthesized DN organohydrogel demonstrates exceptional water retention capabilities,retaining approximately 75% of its original weight even after the exposure to air for 20 days.The Zn MnO_(2) battery delivers an outstanding specific capacity of275 mA h g^(-1) at 1 C,impressive rate performance with 85 mA h g^(-1) at 30 C,and excellent cyclic stability(95% retention after 6000 cycles at 5 C).Zn‖Zn symmetric battery can cycle more than 5000 h at 1 mA cm^(-2) and 1 mA h cm^(-2) without short circuiting.This study will encourage the further development of functional organohydrogel electrolytes for advanced energy storage devices.展开更多
It is still challenging to obtain broadband emission covering visible light spectrum as much as possible with negligible angular dependence. In this work, we demonstrate a low driving voltage top-emitting white organi...It is still challenging to obtain broadband emission covering visible light spectrum as much as possible with negligible angular dependence. In this work, we demonstrate a low driving voltage top-emitting white organic light-emitting diode （TEWOLED） based on complementary blue and yellow phosphor emitters with negligible angular dependence. The bottom copper anode with medium reflectance, which is compatible with the standard complementary metal oxide semiconductor （CMOS） technology below 0.13 μm, and the semitransparent multi- layer Cs2CO3/AI/Cu cathode as a top electrode, are introduced to realize high-performance TEWOLED. Our TEWOLED achieves high efficiencies of 15.4callA and 12.1 1m/W at a practical brightness of lO00cd/m2 at low voltage of 4 V.展开更多
The crevice corrosion behavior of XTO steel was investigated with a wedge-shaped crevice assembly under -1000 m V （SCE） cathodic polarization in the solutions with various HCO3 concentrations. The potential, current...The crevice corrosion behavior of XTO steel was investigated with a wedge-shaped crevice assembly under -1000 m V （SCE） cathodic polarization in the solutions with various HCO3 concentrations. The potential, current, pH and the oxygen content within the crevice were measured with or without outside coupled specimen. The results indicated that the polarization potential of XTO steel in the crevice dropped with the increase of time under the cathodic polarization. There was a remarkable influence of HCO3 concentration on the potential of XTO steel in the crevice. When HCO3 concentration was up to 0.125%, the surface of the metal was covered with the corrosion products that resulted in the polarization extent of XTO steel decreased. The pH value in the crevice rose and it dropped gradually from the crevice mouth to the bottom under the cathodic polarization. With the increasing of HCO3 concentration, the hydrolyzation reaction of metal in the crevice bottom aggravated. Most of the dissolved oxygen in the crevice was consumed by the cathodic current. The maximum cathodic current on the metal surface was at the crevice mouth and it was much more than that at the crevice bottom.展开更多
基金National Natural Science Foundation of China (52372224 and 52072299)Major Project of Shaanxi Coal Joint Fund of Shaanxi Provincial Science and Technology Department (2019JLZ-07)。
文摘Na_(3)V_(2)(PO_(4))_(2)O_(2)F (VP) is recognized as a promising cathode material for sodium-ion batteries due to its stable structural framework and high specific capacity.Density functional theory (DFT) and finite element simulations show that incorporating SO_(4)^(2-)into VP decreases its band gap,lowers the migration energy barrier,and ensures a uniform Na+concentration gradient and stress distribution during charge and discharge cycles.Consequently,the average Na+diffusion coefficient of Na_(3)V_(2)(PO_(4))_(1.95)(SO_(4))_(0.05)O_(2)F(VPS-1) is roughly double that of VP,leading to enhanced rate capability (80 C,75.5 mAh g^(-1)) and cycling stability (111.0 mAh g^(-1)capacity after 1000 cycles at 10 C current density) for VPS-1.VPS-1 exhibits outstanding fast-charging capabilities,achieving an 80%state of charge in just 8.1 min.The assembled VPS-1//SbSn/NPC full cell demonstrated stable cycling over 200 cycles at a high 5 C current,maintaining an average coulombic efficiency of 95.35%.
基金the technical support for Nano-X from Suzhou Institute of Nano-Tech and NanoBionics,Chinese Academy of Sciences(SINANO)supported by the National Key R&D Program of China(2021YFB3800300)+2 种基金the National Natural Science Foundation of China(22179059,22239002,92372201)the science and technology innovation fund for emission peak and carbon neutrality of Jiangsu province(BK20231512,BK20220034)the Key R&D project funded by department of science and technology of Jiangsu Province(BE2020003)。
文摘Aluminum(Al)exhibits excellent electrical conductivity,mechanical ductility,and good chemical compatibility with high-ionic-conductivity electrolytes.This makes it more suitable as an anode material for all-solid-state lithium batteries(ASSLBs)compared to the overly reactive metallic lithium anode and the mechanically weak silicon anode.This study finds that the pre-lithiated Al anode demonstrates outstanding interfacial stability with the Li_6PS_5Cl(LPSCl)electrolyte,maintaining stable cycling for over 1200 h under conditions of deep charge-discharge.This paper combines the pre-lithiated Al anode with a high-nickel cathode,LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2),paired with the highly ionic conductive LPSCl electrolyte,to design an ASSLB with high energy density and stability.Using anode pre-lithiation techniques,along with dual-reinforcement technology between the electrolyte and the cathode active material,the ASSLB achieves stable cycling for 1000 cycles at a 0.2C rate,with a capacity retention rate of up to 82.2%.At a critical negative-to-positive ratio of 1.1,the battery's specific energy reaches up to 375 Wh kg^(-1),and it maintains over 85.9%of its capacity after 100 charge-discharge cycles.This work provides a new approach and an excellent solution for developing low-cost,high-stability all-solid-state batteries.
基金supported by the National Key Research and Development Program of China(Nos.2022YFA1204203 and 2022YFA1204201)Opening Fund of the State Key Laboratory of Optoelectronic Materials and Technologies at Sun Yat-sen University(No.OEMT-2023-KF-01)+1 种基金National Natural Science Foundation of China(Nos.61971463,82272131,and 82202960)the Guangdong Basic and Applied Basic Research Foundation(No.2023A1515010537).
文摘Flat-panel X-ray sources(FPXSs)have many advantages in terms of compactness and low-dose imaging,enhancing their capability for novel X-ray applications.Experimental analysis of the X-ray characteristics and optimizing the anode panel of an FPXS are time-consuming,expensive,and sometimes impractical.In this study,a FPXS was prepared using a ZnO nanowire cold cathode and a molybdenum film anode target.Monte Carlo(MC)simulations were utilized to optimize the anode panel and obtain the average fluence,average energy,and spatial distribution of the X-rays for the ZnO nanowire FPXS.The accuracy of the MC simulations was verified by comparing the measured and simulated energy spectra.Optimization of the anode target considers the material,thickness,and morphology,whereas optimization of the substrate focuses on the material and thickness.The results show that the difference between the positions of the K-shell peaks in the measured and simulated energy spectra is within 0.26 keV.At the acceleration voltages of 30 kV,60 kV,and 90 kV,the optimal thicknesses of the tungsten array anode were 0.65μm,2.45μm,and 5μm,respectively,while the molybdenum array anode has the optimal thicknesses of 1.45μm,5.25μm,and 24μm,respectively.The microsemi-ellipsoidal anode with a recessed design showed a 5%increase in the transmitted X-ray fluence compared with the film target.The sapphire substrate with a thickness of 0.78 mm exhibits a mechanical strength comparable to that of a glass substrate with a thickness of 3 mm,implying that the former can increase the average X-ray fluence by reducing the filtration of X-rays.The findings of this study provide valuable guidance for the fabrication and optimization of the ZnO nanowire FPXS.
基金supported by the National Natural Science Foundation of China(No.52274346).
文摘Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphite.This study utilizes the porous“defect advantage”of a cathode carbon block matrix to prepare silicon-doped and asphalt-coated detoxified and purified waste graphitization cathode carbon blocks for use as high-performance silicon/carbon composite anode materials.The results show that the uniformly silicondoped silicon/carbon composite material features a unique amorphous carbon-encapsulated“locked silicon”structure,which effectively addresses issues such as cathode volume expansion,excessive growth of the solid electrolyte interphase(SEI)film,and poor electrical contact between active materials.Consequently,electrochemical performance is enhanced.After assembly in a half-cell,the PSCC/10%Si@C(purified waste graphitization cathode carbon/10%Si@C)material exhibits optimal electrochemical stability,with an initial charging specific capacity of 514.5 mAh/g at 0.1 C(1 C=170 mA/g)and a capacity retention rate of 95.1%after 100 cycles.At a charge rate of 2.0 C,a specific capacity of 216.9 mAh/g is achieved.This technology provides a new pathway for the economical and high-value utilization of waste cathode carbon blocks and the development of low-cost,high-performance anode materials.
基金financially supported by the Basic Science Center Project of the National Natural Science Foundation of China(No.52388101)Program for Guangdong Introducing Innovative and Entrepreneurial Teams(No.2019ZT08L213)the National Natural Science Foundation of China(No.52100030)。
文摘Flow anodic oxidation system has demonstrated to be a promising and environmental benign water treatment technology because of its advantages of high contaminant removal efficiency and low energy consumption.However,traditional setup needs an external unit for flow anode material separation and recovery,which inevitably increases the capital cost and hinders its continuous operation.Herein,a specific porous cathode is introduced to achieve continuous water purification with high contaminant removal in a flow anodic oxidation system.The efuent concentration of carbamazepine(CBZ),a common and model contaminant widely detected in natural water environment,was reduced by 99%.The linear sweep voltammetry(LSV)and quenching tests demonstrated that HO·was the dominant reactive species.While the removal of contaminants was inhibited in practical surface water,largely related to the quenching by dissolved organic matter and bicarbonate,the flow anodic oxidation process was competent in alleviating the ecotoxicity following oxidation.Our study constructs a modular device for cost-effective continuous water purification and provides insight into the mechanisms of flow andic oxidation.
基金This work was financially supported by the Australian Research Council(ARC)Discovery Projects(DP210103266 and DPI 701048343)the Griffith University Ph.D.Scholarships.
文摘Binders could play crucial or even decisive roles in the fabrication of low-cost, stable and high-capacity electrodes. This is especially the case for the silicon (Si) anodes and sulfur (S) cathodes that undergo large volume change and active material loss in lithium-ion batteries during prolonged cycles. Herein, a hydrophilic polymer poly(methyl vinyl ether-alt-maleic acid) (PMVEMA) was explored as a dual-functional aqueous binder for the preparation of high-performance silicon anode and sulfur cathode. Benefiting from the dual functions of PMVEMA, i.e., the excellent dispersion ability and strong binding forces, the as-prepared electrodes exhibit improved capacity, rate capability and long-term cycling performance. In particular, the as-prepared Si electrode delivers a high initial discharge capacity of 1346.5 mAh g^(−1) at a high rate of 8.4 A/g and maintains 834.5 mAh g^(−1) after 300 cycles at 4.2 A/g, while the as-prepared S cathode exhibits enhanced cycling performance with high remaining discharge capacities of 663.4 mAh g^(−1) after 100 cycles at 0.2 C and 487.07 mAh g^(−1) after 300 cycles at 1 C, respectively. These encouraging results suggest that PMVEMA could be a universal binder to facilitate the green manufacture of both anode and cathode for high-capacity energy storage systems.
文摘To control the power hierarchy design of lithium-ion battery(LIB)builtup sets for electric vehicles(EVs),we offer intensive theoretical and experimental sets of choice anode/cathode architectonics that can be modulated in full-scale LIB built-up models.As primary structural tectonics,heterogeneous composite superstructures of full-cell-LIB(anode//cathode)electrodes were designed in closely packed flower agave rosettes TiO2@C(FRTO@C anode)and vertical-star-tower LiFePO4@C(VST@C cathode)building blocks to regulate the electron/ion movement in the three-dimensional axes and orientation pathways.The superpower hierarchy surfaces and multi-directional orientation components may create isosurface potential electrodes with mobile electron movements,in-to-out interplay electron dominances,and electron/charge cloud distributions.This study is the first to evaluate the hotkeys of choice anode/cathode architectonics to assemble different LIB-electrode platforms with high-mobility electron/ion flows and high-performance capacity functionalities.Density functional theory calculation revealed that the FRTO@C anode and VST-(i)@C cathode architectonics are a superior choice for the configuration of full-scale LIB built-up models.The integrated FRTO@C//VST-(i)@C full-scale LIB retains a huge discharge capacity(~94.2%),an average Coulombic efficiency of 99.85%after 2000 cycles at 1 C,and a high energy density of 127 Wh kg?1,thereby satisfying scale-up commercial EV requirements.
基金financially supported by National Key Research and Development Program of China (No.2019YFC1907805)National Natural Science Foundation of China (No.52004338)+1 种基金Hunan Provincial Natural Science Foundation of China (No.2020JJ5696)Guangdong Provincial Department of Natural Resources (No.2020-011)。
文摘Sodium-ion batteries(SIBs) have gained more scientists’ interest, owing to some facts such as the natural abundance of Na, the similarities of physicochemical characteristics between Li and Na. The irreversible Na+ions consumption during the first cycle of charge/discharge process(due to the formation of the solid electrolyte interface(SEI) on the electrode surface and other irreversible reactions) is the factor that determines high performance SIBs and largely reduces the capacity of the full cell SIBs. Thus, the initial coulombic efficiency(ICE) of SIBs for both anode and cathode materials, is a key parameter for high performance SIBs, and the point is to increase the transport rate of the Na+ions. Therefore, developing SIBs with high ICE and rate performance becomes vital to boost the commercialization of SIBs. Here we provide a review on the methods to improve the ICE and the rate performance, by summarizing some methods of improving the ICE and rate performance of the anode and cathode materials for SIBs, and end by a conclusion with some perspectives and recommendations.
基金financially supported by the National Natural Science Foundation of China(No.21571132)。
文摘Metal anodes based on plating/stripping electrochemistry,for instance,common alkaline metal lithium(Li),sodium(Na),potassium(K),polyvalent metal magnesium(Mg),aluminum(Al),calcium(Ca)and zinc(Zn)are imminently evoked and increasingly researched for future generation high-energy-density rechargeable batteries due to their large theoretical capacity,low electrochemical potential,and superior electronic conductivity in recent years.However,the uncontrolled dendrite formation issue induces low Coulombic efficiency,short lifespan,and hazardous security risks,hindering the actual applications of metal batteries.Among various solutions,the utilization of ferro-/piezoelectric materials for metal anodes displays active effects on decreasing local current density,suppressing dendrite growth,and tolerating volume expansion benefits from the unique ferro-/piezoelectric polarization effect.This review presents the research progress of ferro-/piezoelectric polarization effect for regulating the dendritic growth of metal anodes for the first time.First,the current challenges and strategies of metal anodes are proposed.Then,ferro-/piezoelectric materials and their working principle are discussed.Finally,the recent research progress of ferroelectric and piezoelectric materials on dynamic regulation of dendrite growth is summarized,and the future perspectives are prospected.We hope this review could draw more attention in designing metal anodes with self-polarization materials and promoting their practical applications.
基金Projects(11304243,11102164)supported by the National Natural Science Foundation of ChinaProject(2014JQ1039)supported by the Natural Science Foundation of Shannxi Province,China+3 种基金Project(12JK0966)supported by the Shaanxi Provincial Education Department,ChinaProject(2013QDJ037)supported by the Xi’an University of Science and Technology Dr Scientific Research Fund,ChinaProject(3102016ZY027)supported by the Fundamental Research Funds for the Central Universities of ChinaProject(13GH014602)supported by the Program of New Staff and Research Area Project of NPU,China
文摘This work presents a method to solve the weak solubility of zinc chloride(ZnCl_2) in the ethanol by adding some reasonable water into an ethanol electrolyte containing ZnCl_2 and myristic acid(CH_3(CH_2)_(12)COOH).A rapid one-step electrodeposition process was developed to fabricate anodic(2.5 min) and cathodic(40 s) superhydrophobic surfaces of copper substrate(contact angle more than 150°) in an aqueous ethanol electrolyte.Morphology,composition,chemical structure and superhydrophobicity of these superhydrophobic surfaces were investigated by SEM,FTIR,XRD,and contact angle measurement,respectively.The results indicate that water ratio of the electrolyte can reduce the required deposition time,superhydrophobic surface needs over 30 min with anhydrous electrolyte,while it needs only 2.5 min with electrolyte including 10 mL water,and the maximum contact angle of anodic surface is 166° and that of the cathodic surface is 168°.Two copper electrode surfaces have different reactions in the process of electrodeposition time,and the anodic copper surface covers copper myristate(Cu[CH_3(CH_2)_(12)COO]_2) and cupric chloride(CuCl);while,zinc myristate(Zn[CH_3(CH_2)_(12)COO]_2) and pure zinc(Zn) appear on the cathodic surface.
基金supported by the National Key Research and Development Program of China(2021YFB3800300,2018YFE0206900)the National Natural Science Foundation of China(52072138)the technical support from the Analytical and Testing Center of Huazhong University of Science and Technology(HUST)。
文摘Poly(ethylene oxide)(PEO)-based solid polymer electrolyte is always the most promising candidate for preparing thinner, lighter and safer lithium-ion batteries. However, the lithium dendrites growth of lithium anode and the high-voltage oxidation of cathode are easy to cause the PEO-based battery failure.The way to deal with the different challenges on both sides of the anode and cathode is pursued all the time. In this study, we reported a new strategy to construct the PVDF/PEO/PVDF three-layer structure for solid polymer electrolyte(marked as PVDF@PEO) using PVDF as the functional “skin”. The PVDF@PEO electrolyte can effectively prevent from the lithium dendrites, and shows a stable cycling life over1000 h in the Li/PVDF@PEO/Li cell. In addition, the PVDF@PEO electrolyte exhibits higher oxidation resistance and can be matched with high-voltage LiCoO_(2) cathode. The Li/PVDF@PEO/LiCoO_(2) cell delivered a specific capacity of about 150 m Ah g^(-1) over 150 cycles and maintained good cycling stability. Our research provides insights that the polymer electrolytes constructed with PVDF functional “skin” can simultaneously meet the challenges of both anode and cathode in solid-state lithium-ion batteries(SSLIBs).
基金financial support by the National Natural Science Foundation of China(No.91963118)Fundamental Research Funds for the Central Universities(No.2412019ZD010)。
文摘Dual ion batteries(DIBs) exhibit broad application prospects in the field of electrical energy storage(EES)devices with excellent properties,such as high voltage,high energy density,and low cost.In the graphitebased DIBs,high voltage is needed to store enough anions with the formation of anion intercalation compound XCn(X=AlCl4-,PF6-,TFSI-,etc.).Hence,it is difficult for graphite-based DIBs to match proper anodes and electrolytes.Here,an Se/graphene composite is prepared via a convenient method,and assembled into a dual-ion full battery(DIFB) as anode with graphite cathode and 1 mol/L NaPF6 in EC:EMC(1:1,v:v).This DIFB has achieved a high discharge capacity of 75.9 mAh/g and high medium output voltage of 3.5 V at 0.1 A/g.Actually,the suitable anode materials,such as the present Se/graphene composite,are extremely important for the development and application of graphite-based DIBs.This study is enlightening for the design of future low-cost EES devices including graphite-based DIBs.
文摘In this paper, the effects of zinc （Zn） and magnesium （Mg） addition on the performance of an aluminum-based sacrificial anode in seawater were investigated using a potential measurement method. Anodic efficiency, protection efficiency, and polarized potential were the parameters used. The percentages of Zn and Mg in the anodes were varied from 2% to 8% Zn and 1% to 4% Mg. The alloys produced were tested as sacrificial anodes for the protection of mild steel in seawater at room temperature. Current efficiency as high as 88.36% was obtained in alloys containing 6% Zn and 1% Mg. The polarization potentials obtained for the coupled （steel/Al-based alloys） are as given in the Pourbaix diagrams, with steel lying within the immunity region/cathodic region and the sacrificial anodes within the anodic region. The protection offered by the sacrificial anodes to the steel after the 7th and 8th week was measured and protection efficiency values as high as 99.66% and 99.47% were achieved for the A1-6%Zn-l%Mg cast anode. The microstructures of the cast anodes comprise of intermetallic structures of hexagonal Mg3Zn2 and body-centered cubic A12Mg3Zn3. These are probably responsible for the breakdown of the passive alumina film, thus enhancing the anode efficiency.
基金the support by the Key-Area Research and Development Program of Guangdong Province(No.2020B090919003)the National Nature Science Foundation of China(Nos.51872157 and 52072208)+4 种基金the Shenzhen Technical Plan Project(Nos.JCYJ20170817161753629 and JCYJ20170412170911187)the Special Fund Project for Strategic Emerging Industry Development of Shenzhen(No.20170428145209110)the Local Innovative and Research Teams Project of Guangdong Pearl River Talents Program(No.2017BT01N111)the Support Plan for Shenzhen Manufacturing Innovation Center(No.20200627215553988)the Key projects for core technology research of Dongguan(No.2019622119003)。
文摘The energy density of commercial lithium(Li)ion batteries with graphite anode is reaching the limit.It is believed that directly utilizing Li metal as anode without a host could enhance the battery’s energy density to the maximum extent.However,the poor reversibility and infinite volume change of Li metal hinder the realistic implementation of Li metal in battery community.Herein,a commercially viable hybrid Li-ion/metal battery is realized by a coordinated strategy of symbiotic anode and prelithiated cathode.To be specific,a scalable template-removal method is developed to fabricate the porous graphite layer(PGL),which acts as a symbiotic host for Li ion intercalation and subsequent Li metal deposition due to the enhanced lithiophilicity and sufficient ion-conducting pathways.A continuous dissolution-deintercalation mechanism during delithiation process further ensures the elimination of dead Li.As a result,when the excess plating Li reaches 30%,the PGL could deliver an ultrahigh average Coulombic efficiency of 99.5% for 180 cycles with a capacity of 2.48 m Ah cm^(-2) in traditional carbonate electrolyte.Meanwhile,an air-stable recrystallized lithium oxalate with high specific capacity(514.3 m Ah g^(-1))and moderate operating potential(4.7-5.0 V)is introduced as a sacrificial cathode to compensate the initial loss and provide Li source for subsequent cycles.Based on the prelithiated cathode and initial Li-free symbiotic anode,under a practical-level3 m Ah capacity,the assembled hybrid Li-ion/metal full cell with a P/N ratio(capacity ratio of Li Ni_(0.8)Co_(0.1)Mn_(0.1)O_(2) to graphite)of 1.3exhibits significantly improved capacity retention after 300 cycles,indicating its great potential for high-energy-density Li batteries.
文摘Vacuum space between Ar atoms in unlighted HCFL lamps is an electric insulator, because vacuum fills up with strong negative electric field from orbital electrons in 3p6 electron shell of Ar atoms. Vacuum space in lighted FL lamps changes to the neutral vacuum that provides a superconductive vacuum for moving electrons at above room temperature. The complications of lighting mechanisms of HCFL lamps for more than 80 years have clearly solved with coexistence of disparate external and internal electric circuits for each half cycle. External electric circuit acts as two roles. One helps for formation of internal electric circuit in Ar gas space by electric field. Other picks up induced voltages from capacitor CFL. HCFL lamp only lights up with moving electrons in internal DC driving circuit. Electrons in HCFL lamp only move from cathode to anode, which respectively have negative and positive potentials against grand (V = 0), and which are formed with volumes of heated corona light (4G) at around W-filament metal electrodes with a help of heated BaO particles. The HCFL lamp that emits thermoelectrons is a false story. Here we have totally revised the fundamentals of the lighting mechanism of the established HCFL lamps for last 80 years.
基金the National Science Foundation and Advanced Technologies(NFSAT),the grant No.TFP-12-06supported by Clarkson University Mechanical and Aeronautical Engineering Department,and Clarkson University Center for Advanced Material Processing
文摘Experimental investigations and associated methods are provided to characterize the mechanical properties of a lithium-ion battery accounting for operating temperature variation and thermal effects. Material properties for LiFeP04 cathode and anode samples taken from an off-the-shelf battery are evaluated in new and fatigued （subjec- ted to charging and discharging cycles） conditions.
基金Joint Funds of the National Natural Science Foundation of China (U22A20140)University of Jinan Disciplinary Cross-Convergence Construction Project 2023 (XKJC-202309, XKJC-202307)+4 种基金Jinan City-School Integration Development Strategy Project (JNSX2023015)Independent Cultivation Program of Innovation Team of Ji’nan City (202333042)Youth Innovation Group Plan of Shandong Province (2022KJ095)Shenzhen Stable Support Plan Program for Higher Education Institutions Research Program (20220816131408001)Shenzhen Science and Technology Program (JCYJ20230807091802006)。
文摘Current aqueous battery electrolytes,including conve ntional hydrogel electrolytes,exhibit unsatisfactory water retention capabilities.The sustained water loss will lead to subsequent polarization and increased internal resistance,ultimately resulting in battery failure.Herein,a double network(DN) orga no hydrogel electrolyte based on dimethyl sulfoxide(DMSO)/H_(2)O binary solvent was proposed.Through directionally reconstructing hydrogen bonds and reducing active H_(2)O molecules,the water retention ability and cathode/anode interfaces were synergistic enhanced.As a result,the synthesized DN organohydrogel demonstrates exceptional water retention capabilities,retaining approximately 75% of its original weight even after the exposure to air for 20 days.The Zn MnO_(2) battery delivers an outstanding specific capacity of275 mA h g^(-1) at 1 C,impressive rate performance with 85 mA h g^(-1) at 30 C,and excellent cyclic stability(95% retention after 6000 cycles at 5 C).Zn‖Zn symmetric battery can cycle more than 5000 h at 1 mA cm^(-2) and 1 mA h cm^(-2) without short circuiting.This study will encourage the further development of functional organohydrogel electrolytes for advanced energy storage devices.
基金Supported by the National Basic Research Program of China under Grant No 2010CB327701the National Natural Science Foundation of China under Grant No 61275033
文摘It is still challenging to obtain broadband emission covering visible light spectrum as much as possible with negligible angular dependence. In this work, we demonstrate a low driving voltage top-emitting white organic light-emitting diode （TEWOLED） based on complementary blue and yellow phosphor emitters with negligible angular dependence. The bottom copper anode with medium reflectance, which is compatible with the standard complementary metal oxide semiconductor （CMOS） technology below 0.13 μm, and the semitransparent multi- layer Cs2CO3/AI/Cu cathode as a top electrode, are introduced to realize high-performance TEWOLED. Our TEWOLED achieves high efficiencies of 15.4callA and 12.1 1m/W at a practical brightness of lO00cd/m2 at low voltage of 4 V.
基金the National R&D Infrastructure and Facility Development Program of China(No.2005DKA10400)Financial support from the National Key Technology R&D Program of China (No.2006BAKO2B01-06)is also acknowledged.
文摘The crevice corrosion behavior of XTO steel was investigated with a wedge-shaped crevice assembly under -1000 m V （SCE） cathodic polarization in the solutions with various HCO3 concentrations. The potential, current, pH and the oxygen content within the crevice were measured with or without outside coupled specimen. The results indicated that the polarization potential of XTO steel in the crevice dropped with the increase of time under the cathodic polarization. There was a remarkable influence of HCO3 concentration on the potential of XTO steel in the crevice. When HCO3 concentration was up to 0.125%, the surface of the metal was covered with the corrosion products that resulted in the polarization extent of XTO steel decreased. The pH value in the crevice rose and it dropped gradually from the crevice mouth to the bottom under the cathodic polarization. With the increasing of HCO3 concentration, the hydrolyzation reaction of metal in the crevice bottom aggravated. Most of the dissolved oxygen in the crevice was consumed by the cathodic current. The maximum cathodic current on the metal surface was at the crevice mouth and it was much more than that at the crevice bottom.
