For the diagnostics and health management of lithium-ion batteries,numerous models have been developed to understand their degradation characteristics.These models typically fall into two categories:data-driven models...For the diagnostics and health management of lithium-ion batteries,numerous models have been developed to understand their degradation characteristics.These models typically fall into two categories:data-driven models and physical models,each offering unique advantages but also facing limitations.Physics-informed neural networks(PINNs)provide a robust framework to integrate data-driven models with physical principles,ensuring consistency with underlying physics while enabling generalization across diverse operational conditions.This study introduces a PINN-based approach to reconstruct open circuit voltage(OCV)curves and estimate key ageing parameters at both the cell and electrode levels.These parameters include available capacity,electrode capacities,and lithium inventory capacity.The proposed method integrates OCV reconstruction models as functional components into convolutional neural networks(CNNs)and is validated using a public dataset.The results reveal that the estimated ageing parameters closely align with those obtained through offline OCV tests,with errors in reconstructed OCV curves remaining within 15 mV.This demonstrates the ability of the method to deliver fast and accurate degradation diagnostics at the electrode level,advancing the potential for precise and efficient battery health management.展开更多
Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-car...Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-carbon emissions and no chlorine gas evolution.The clean production stems from the choice of a molten NaCl-Na_(2)CO_(3) electrolyte to prevent chlorine gas evolution,an inert nickel-based anode to produce oxygen,and a liquid metal cathode to make the cathodic product sit at the bottom of the electrolytic cell.We achieve a current efficiency of>90%for the electrolytic production of liquid Na-Sn alloy.Later,Mg-Sn alloy is prepared using the obtained Na-Sn alloy to displace Mg from molten NaCl-MgCl_(2) with a displacement efficiency of>96%.Further,Na and Mg are separated from the electrolytic Na-Sn and displaced Mg-Sn alloys by vacuum distillation with a recovery rate of>92%and Sn can be reused.Using this electrolysisdisplacement-distillation(EDD)approach,we prepare Mg from seawater.The CO_(2)emission of the EDD approach is~20.6 kg CO_(2)per kg Mg,which is less than that of the Australian Magnesium(AM)electrolysis process(~25.0 kg CO_(2)per kg Mg)and less than half that of the Pidgeon process(~45.2 kg CO_(2)per kg Mg).展开更多
Improving the volumetric energy density of supercapacitors is essential for practical applications,which highly relies on the dense storage of ions in carbon-based electrodes.The functional units of carbon-based elect...Improving the volumetric energy density of supercapacitors is essential for practical applications,which highly relies on the dense storage of ions in carbon-based electrodes.The functional units of carbon-based electrode exhibit multi-scale structural characteristics including macroscopic electrode morphologies,mesoscopic microcrystals and pores,and microscopic defects and dopants in the carbon basal plane.Therefore,the ordered combination of multi-scale structures of carbon electrode is crucial for achieving dense energy storage and high volumetric performance by leveraging the functions of various scale structu re.Considering that previous reviews have focused more on the discussion of specific scale structu re of carbon electrodes,this review takes a multi-scale perspective in which recent progresses regarding the structureperformance relationship,underlying mechanism and directional design of carbon-based multi-scale structures including carbon morphology,pore structure,carbon basal plane micro-environment and electrode technology on dense energy storage and volumetric property of supercapacitors are systematically discussed.We analyzed in detail the effects of the morphology,pore,and micro-environment of carbon electrode materials on ion dense storage,summarized the specific effects of different scale structures on volumetric property and recent research progress,and proposed the mutual influence and trade-off relationship between various scale structures.In addition,the challenges and outlooks for improving the dense storage and volumetric performance of carbon-based supercapacitors are analyzed,which can provide feasible technical reference and guidance for the design and manufacture of dense carbon-based electrode materials.展开更多
Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batterie...Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batteries for mitigating range anxiety and slow charging issues in new energy vehicles.Herein,a thick silicon/carbon composite electrode with vertically aligned channels in the thickness direction(VC-SC)is constructed by employing a bubble formation method.Both experimental characterizations and theoretical simulations confirm that the obtained vertical channel structure can effectively address the problem of sluggish ion transport caused by high tortuosity in conventional thick electrodes,conspicuously enhance reaction kinetics,reduce polarization and side reactions,mitigate stress,increase the utilization of active materials,and promote cycling stability of the thick electrode.Consequently,when paired with LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622),the VC-SC||NCM622 pouch type full cell(~6.0 mAh cm^(-2))exhibits significantly improved rate performance and capacity retention compared with the SC||NCM622 full cell with the conventional silicon/carbon composite electrode without channels(SC)as the anode.The assembled VC-SC||NCM622 pouch full cell with a high energy density of 490.3 Wh kg^(-1)also reveals a remarkable fast charging capability at a high current density of 2.0 mA cm^(-2),with a capacity retention of 72.0%after 500 cycles.展开更多
Introduction The generation of biological wastes such as cow dung and aloe vera waste(AVW)causes a serious ecological pollution.The microbial electrolytic cell coupled with anaerobic digestion(MEC-AD)system can make a...Introduction The generation of biological wastes such as cow dung and aloe vera waste(AVW)causes a serious ecological pollution.The microbial electrolytic cell coupled with anaerobic digestion(MEC-AD)system can make a rational utilization of these biodegradable organic wastes,which is of vital importance for alleviating environmental deterioration and reducing resource waste.Electrode materials and accelerants are the two major factors that affect methane production in the MEC-AD system.They affect microbial attachment and electron transfer in the MEC-AD system.Bio-based carbon materials are carbon materials prepared from biomass as raw materials.They have characteristics such as a rich pore structure,good chemical stability,biocompatibility,and controllable surface properties,which can be used as accelerants and electrodes in the MEC-AD system to optimize its performance.This study was to investigate the influence of biomass-derived carbon as an electrode and accelerant on the performance of the MEC-AD system,and the mechanism for increasing the production of biogas and methane was also analyzed,thus providing a basis for the multifunctional application of biomass-derived carbon in the MEC-AD system.Methods A series of experimental methods were adopted to study the MEC-AD system.Two types of bio-based carbon,i.e.,aloe vera waste derived spherical carbon(AVW-SC)and porous carbon(AVW-PC),were synthesized via hydrothermal carbonization.The raw AVW material was washed with water,dried,ground,and subjected to hydrothermal treatment to obtain AVW-SC.After activating AVW-SC with KOH,it was carbonized in a tube furnace to obtain AVW-PC.In the preparation of the electrodes,bio-based carbon(AVW-SC and AVW-PC)was mixed with 5%polytetrafluoroethylene powder in ethanol and deionized water,and then ground in a ball mill for 4 h to form a slurry.The slurry was evenly sprayed on the Ti mesh,dried and sintered in N2 atmosphere at 360℃to obtain Ti-SC and Ti-PC electrodes.Four groups of experiments were conducted to determine the optimal voltage,compare different carbon electrodes,and explore the optimal coating amount.The MEC-AD reactor adopted 500 mL wide-mouthed glass bottles with a working volume of 400 mL.Each MEC-AD system received a co-substrate mixture of cattle dung and aloe vera waste and inoculum of sewage sludge in a mass ratio of 3:7.Afterward,they were placed at(36±1)℃for 35 d.The biogas was collected by a water displacement method.The materials were analyzed by characterization techniques such as X-ray diffraction(XRD)and scanning electron microscopy(SEM),and electrochemical tests were conducted on different electrodes.The composition,pH,TS,VS,TCOD and nutrient content of biogas were analyzed by standard chemical methods.Microbial community analysis was conducted using high-throughput sequencing technology.The modified Gompertz model was adopted to predict the kinetic parameters,and the coulombic efficiency and methane recovery rate were calculated according to a specific formula.Results and discussion The result shows that AVW-SC is spherical and closely aggregated,while AVW-PC has a three-dimensional network structure,with average pore diameter of 9.77 nm.The electron exchange capacity(EEC)of AVW-PC(i.e.,0.75μmol·e-/g)is higher than that of AVW-SC(i.e.,0.15μmol·e-/g),indicating a better electron exchange capacity.These results indicate that AVW-PC provides more substrate and bacteria accumulation sites,and has better electron-donating and electron-accepting ability,thus improving the digestion efficiency.In the MEC-AD system,using Ti mesh as an electrode,the effect of different voltages(i.e.,0,0.4,0.6,0.8 V and 1.2 V)on the system performance is investigated,obtaining the optimum biogas production and organic matter degradation rate at 0.8 V.AVW-SC and AVW-PC are respectively coated on Ti mesh as electrodes.The results show that the MEC-AD system with AVW-PC coated Ti mesh as the electrode has a better performance.The electrochemical analysis shows that the electrode coated with AVW-PC has a larger specific capacitance and a smaller charge transfer resistance,indicating that AVW-PC can improve the electrochemical properties and electron transfer ability of MEC-AD system.The influence of coating amount(i.e.,0.025,0.05,0.10,0.15,and 0.20 g)of AVW-PC on the MEC-AD system is investigated.At a coating amount of AVW-PC of 0.1 g,the cumulative biogas production and methane content of the Ti_(0.8)-PC_90.1) group both reach the maximum values.Different doses of AVW-PC(i.e.,0.10%,0.15%,0.20%,and 0.25%)are added as accelerants in Ti_(0.8)-PC_90.1).At the addition amount of AVW-PC of 0.20%,the Ti_(0.8)-PC_90.1)/PC0.2 group performs the optimum biogas production(i.e.,633.63 mL/g VS),methane content(i.e.,65.85%),and total nutrient content of biogas residue(i.e.,42.30 g/kg).In Ti_(0.8)-PC_90.1)/PC0.2,Bacteroidales,Pseudomonadales,Oscillospirales,Methanobacteraceae,Methanospirillaceae,Methanosarcinacea and Methanosaetaceae significantly increase.The increase in microbial diversity promotes interspecific hydrogen transfer(IHT),interspecific acetic transfer(IAT),and direct interspecific electron transfer(DIET),thereby enhancing methanogenic efficiency.Conclusions AVW-SC and AVW-PC were utilized as electrodes and accelerants to enhance methane yield in MEC-AD system.The Ti mesh electrode coated with different concentrations of AVW-PC achieved the optimal biogas production at 0.8 V.Specifically,the Ti_(0.8)-PC_90.1) combination could generate the maximum total amount of biogas and methane proportion.The Ti_(0.8)-PC_90.1)/PC0.2 combination exhibited the optimum performance(i.e.,biogas yield of 633.63 mL/g VS,methane content of 65.85%and total nutritional content of 42.30 g/kg).High abundances of Bacteroidales,Pseudomonadales,Oscillospirales,Methanobacteraceae,Methanospirillaceae,Methanosarcinaceae,and Methanosaetaceae appeared in the Ti_(0.8)-PC_90.1)/PC0.2 group,compared to other groups.In addition,an increased microbial diversity led to an enhanced methane production through processes like DIET.This research could highlight the potential significance of AVW-PC as both electrode and accelerator for increasing methane production and provide a perspective for improving MEC-AD performance through multiple applications of biomass-derived carbon.展开更多
As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation ...As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation and fragmentation.This ultimately leads to a decrease in cell capacity.The trends of volume expansion and capacity change of the SiO/graphite(SiO/C)composite electrode during cycling were investigated via in situ expansion monitoring.First,a series of expansion test schemes were designed,and the linear relationship between negative electrode expansion and cell capacity degradation was quantitatively analyzed.Then,the effects of different initial pressures on the long-term cycling performance of the cell were evaluated.Finally,the mechanism of their effects was analyzed by scanning electron microscope.The results show that after 50 cycles,the cell capacity decreases from 2.556 mAh to 1.689 mAh,with a capacity retention ratio(CRR)of only 66.08%.A linear relationship between the capacity retention ratio and thickness expansion was found.Electrochemical measurements and scanning electron microscope images demonstrate that intense stress inhibits the lithiation of the negative electrode and that the electrode is more susceptible to irreversible damage during cycling.Overall,these results reveal the relationship between the cycling performance of SiO and the internal pressure of the electrode from a macroscopic point of view,which provides some reference for the application of SiO/C composite electrodes in lithium-ion batteries.展开更多
Rapid developments in lithium-ion battery(LIB)technology have been fueled by the expanding market for electric vehicles and increased demands for energy storage.Recently,thick electrode fabrication by solvent-free met...Rapid developments in lithium-ion battery(LIB)technology have been fueled by the expanding market for electric vehicles and increased demands for energy storage.Recently,thick electrode fabrication by solvent-free methods has emerged as a promising strategy for enhancing the energy density of LIBs.However,as electrode thickness increases,the tortuosity of lithium-ion transport also increases,resulting in severe polarization and poor electrochemical performance.Here,we investigate the effect of conductive agent morphology on the structural and electrochemical properties of 250μm thick lithium iron phosphate(LFP)/conductive agent/polytetrafluoroethylene(PTFE)-based electrodes.Three commercially available conductive additives,namely 0D Super P,1D multi-walled carbon nanotubes(MWCNTs),and 2D graphene nanoplatelets(GNPs),were incorporated into LFP-based electrodes.The MWCNT-incorporated electrode with a high loading mass(42 mg cm^(-2))exhibited a high porosity(ε=51%)and low tortuosity(τ=4.02)owing to its highly interconnected fibrous network of MWCNTs.Due to the fast lithium-ion transport kinetics in the MWCNT-incorporated electrode,the electrochemical performances exhibited a high specific capacity of 157 mAh g^(-1)at 0.1 C and an areal capacity of 7.16 mAh cm^(-2)at 0.1 C with a high-rate capability and excellent cycling stability over 300 cycles at 0.1 C.This study provides a guidance for utilizing conductive agents to apply in the low tortuous thick electrode fabricated by a solvent-free process.Additionally,this work paves the way to achieve scalable and sustainable dry processing techniques for developing next-generation energy storage technologies.展开更多
Silver nanowires(Ag NWs)have promising application potential in electronic displays because of their superior flexibility and transparency.Doping Ni in Ag NWs has proven to be an effective strategy to im-prove its wor...Silver nanowires(Ag NWs)have promising application potential in electronic displays because of their superior flexibility and transparency.Doping Ni in Ag NWs has proven to be an effective strategy to im-prove its work function.However,AgNi NWs-based electrodes suffer from poor electrical conductivity under air exposure due to the low-conductivity NiO generated on its surface.Here,Cu was further doped in AgNi NWs to form AgNiCu NWs and regulate its surface oxide under long-term air exposure.Finally,it is demonstrated that the conductivity of AgNiCu NWs can acquire an improved tolerable tempera-ture(over 240℃)and prolonged high-temperature tolerance time(over 150 min)by finely regulating the doping content Cu,indicating an enhanced air-stable conductivity.The optimized AgNiCu NWs also achieve superior transparent conductivity as pure Ag NWs and high work function as AgNi NWs,which has been successfully applied in constructing an n-type photodiode with an effective rectification effect.展开更多
Amidst the ever-growing interest in high-mass-loading Li battery electrodes,a persistent challenge has been the insufficient continuity of their ion/electron conduction pathways.Here,we propose cellulose elementary fi...Amidst the ever-growing interest in high-mass-loading Li battery electrodes,a persistent challenge has been the insufficient continuity of their ion/electron conduction pathways.Here,we propose cellulose elementary fibrils(CEFs)as a class of deagglomerated binder for high-mass-loading electrodes.Derived from natural wood,CEF represents the most fundamental unit of cellulose with nanoscale diameter.The preparation of the CEFs involves the modulation of intermolecular hydrogen bonding by the treatment with a proton acceptor and a hydrotropic agent.This elementary deagglomeration of the cellulose fibers increases surface area and anionic charge density,thus promoting uniform dispersion with carbon conductive additives and suppressing interfacial side reactions at electrodes.Consequently,a homogeneous redox reaction is achieved throughout the electrodes.The resulting CEF-based cathode(overlithiated layered oxide(OLO)is chosen as a benchmark electrode active material)exhibits a high areal-mass-loading(50 mg cm^(-2),equivalent to an areal capacity of 12.5 mAh cm^(-2))and a high specific energy density(445.4 Wh kg–1)of a cell,which far exceeds those of previously reported OLO cathodes.This study highlights the viability of the deagglomerated binder in enabling sustainable high-mass-loading electrodes that are difficult to achieve with conventional synthetic polymer binders.展开更多
High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic system...High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic systems remains challenging.Here,we conduct comprehensive investigations into the electrochemical properties and structu ral evolution of(CrMnCoNiZn)_(3)O_(4)(HESO)to clarify lithium storage mechanisms.Density functional theory(DFT)calculations reveal that polycationic synergy modulates the electronic structure and d-band centers of HESO,delivering fast electrode kinetics.Exhaustive in-and exsitu analyses demonstrate that the residual crystalline phases acting as seed crystals maintain the spinel/rock-salt lattice persistence under the entropy stabilization effect,lattice distortion effect,and cation synergy,which guide cation crystallization upon the electric field to drive reversible lithium storage.Such properties underlie the HESO electrode with an exceptional rate and long-term capability.This work clarifies the roles of cationic synergy and seed-crystal-driven structural reversibility,providing a blueprint for designing high-performance HEO negative electrodes for next-generation lithium-ion batteries(LIBs).展开更多
Boron-doped diamond(BDD)is a well-known anode material with a high pollutant degradation ability for electrochemical oxidation wastewater treatment.Nevertheless,the cost of production and mechanical strength of BDD me...Boron-doped diamond(BDD)is a well-known anode material with a high pollutant degradation ability for electrochemical oxidation wastewater treatment.Nevertheless,the cost of production and mechanical strength of BDD membranes remain unsatisfactory.Magnetic BDD particles derived from industrial waste may represent a promising alternative to BDD membranes,although the challenge remains in assembling these particles into a usable electrode.In this study,magnetic BDD particles were attracted to a Ti/RuO_(2)-IrO_(2)electrode using a magnet,thus constituting a novel 2.5-dimensional(2.5D)electrode.To ascertain the structure-activity relationship of the novel electrode,essential characterizations,multi-physics simulations,pollutant degradation and electrosynthesis experiments were conducted.The results indicate that an appropriate quantity of BDD particles(0.1 g/cm^(2))can enhance the number of active sites by approximately 20%.A strong synergistic effect was observed between the Ti/Ti/RuO_(2)-IrO_(2)and BDD particles in the degradation of various pollutants,including azo dye,p-benzoquinone,succinic acid and four kinds of real wastewaters,as well as glycerol conversion.The joint active sites on the interface between Ti/RuO_(2)-IrO_(2)and BDD particles,as well as the inner active sites on BDD particles,have been identified as crucial in the mineralization of pollutants and the generation of value-added products.The optimal amount of BDD particles(0.1 g/cm^(2))is sufficient to preserve the joint active sites and to maintain an adequate polarization on the BDD particles.Nevertheless,the hybrid feature of the 2.5D electrode is diminished when a greater quantity of BDD particles(0.3 g/cm^(2))is loaded.展开更多
Silicon monoxide(SiO)is highly attractive as an anode material for high-energy lithium-ion batteries(LIBs)due to its significantly higher specific capacity.However,its practical application is hindered by substantial ...Silicon monoxide(SiO)is highly attractive as an anode material for high-energy lithium-ion batteries(LIBs)due to its significantly higher specific capacity.However,its practical application is hindered by substantial volume expansion during cycling,which leads to material pulverization and an unstable solid electrolyte interphase(SEI)layer.Inspired by the natural root fixation in soil,we designed a root-like topological structure binder,cassava starch-citric acid(CS-CA),based on the synergistic action of covalent and hydrogen bonds.The abundant-OH and-COOH groups in CS-CA molecules effectively form hydrogen bonds with the-OH groups on the SiO surface,significantly enhancing the interfacial interaction between CS-CA and SiO.The root-like topological structure of CS-CA with a high tolerance alleviates the mechanical stress generated by the volume changes of SiO.More encouragingly,the hydrogen bond action among CS-CA molecules produces a self-healing effect,which is advantageous for repairing damaged electrodes and preserving their structural integrity.As such,the CS-CA/SiO electrode exhibits exceptional cycling performance(963.1 mA h g^(-1)after 400 cycles at 2 A g^(-1))and rate capability(558.9 mA h g^(-1)at 5 A g^(-1)).This innovative,topologically interconnected,root-inspired binder will greatly advance the practical application of long-lasting micron-sized SiO anodes.展开更多
Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous deman...Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous demand for sustainable energy storage while limiting Li sources for Li-based batteries.However,the much larger size of the K-ion usually leads to the serious electrodes'volumetric expansion with rapid capacity fading,making the pursuit of electrodes for potassium storage with high capacity and high stability a significant challenge.The polymer electrode materials have been considered promising materials to address these issues due to their porous characteristics,insolubility in electrolytes,and flexible structural design at a molecular level.In this review,we outline the recent advancements in redox-active polymer electrodes,including anode and cathode,materials for K-based batteries,including crystalline porous coordination polymers,crystalline covalent organic polymers,amorphous polymers,and polymer composites.We discuss the electrode designs,electrochemical performances,and K-ion storage mechanism,with a focus on their structure-function correlations.With this knowledge,we propose the perspectives and challenges in designing advanced polymer electrode materials for K-based batteries.We expect this review will shed light on the further development of reliable polymer electrode materials.展开更多
Rechargeable magnesium batteries(RMBs)have attracted much attention due to the high theoretical capacity(3833 mAh cm−3)of magnesium metal negative electrode and abundant resources.However,the preparation of ultra-thin...Rechargeable magnesium batteries(RMBs)have attracted much attention due to the high theoretical capacity(3833 mAh cm−3)of magnesium metal negative electrode and abundant resources.However,the preparation of ultra-thin magnesium foils faces the problems of rolling difficulty and high processing cost,while the use of thick magnesium foils leads to low utilization of magnesium and reduces the energy density.To tackle the above problems,we successfully prepared ultra-thin magnesium foils based on electrolytic process and investigated the effect of different substrates.The magnesium foils prepared using Mo substrate have more uniform surface morphology and lower surface roughness,which is attributed to the lower magnesium nucleation overpotential of Mo substrate.Meanwhile,density functional theory calculations show that the adsorption energy of Mo on Mg is more negative,which is conducive to achieving uniform nucleation and deposition of Mg.The Mg deposition on Mo substrate undergoes the characteristic stages of transient nucleation,nucleus accretion,multidirectional heterotopic growth,and columnar crystal stacking,and ultimately the formation of a dense deposited layer.In addition,the prepared ultra-thin Mg foil with Mo substrate can stably cycle for 1000 h at 3 mA cm^(-2) with high utilization of 50% in the symmetric cell.This study develops a facile method for the preparation of ultra-thin Mg foils,which opens up a new path for developing high-performance ultra-thin negative electrodes for RMBs.展开更多
Anion exchange membrane fuel cells(AEMFCs)are considered a more affordable technology compared to proton exchange membrane fuel cells(PEMFCs),but the performance and durability of AEMFCs are still not competent with P...Anion exchange membrane fuel cells(AEMFCs)are considered a more affordable technology compared to proton exchange membrane fuel cells(PEMFCs),but the performance and durability of AEMFCs are still not competent with PEMFCs owing to the more challenging water management,which severely hinders its development and real-life applications.In this study,we introduce the strategy to boost the performance and stability of the membrane electrode assembly(MEA)of AEMFCs by regulating the hydrophilicity of the anode and cathode ionomers.Two poly(biphenyl alkylene)ionomers with different hydrophilicity are synthesized and used to fabricate MEAs with asymmetric or symmetric ionomer configurations in the anodic and cathodic catalyst layers(CLs)for AEMFCs.Molecular dynamics(MD)simulations have revealed different diffusion rates of water in the hydrophobic anode and the hydrophilic cathode,which show the potential of this design to improve water management in AEMFCs,The effectiveness of this design is also confirmed by experimental results that the MEA with this asymmetric configuration exhibits the highest power and current densities of 1.58 W cm^(-2)or 5.58 A cm^(-2),respectively,among all configurations.Furthermore,this configuration also enhances the durability,with the MEA showing a voltage decay rate of only 313.1μV h^(-1)after 500 h of in-situ durability test at 0.2 A cm^(-2).This study provides new insights into the rational design of more efficient water management in MEA for high-performance AEMFCs.展开更多
Multifunctional flexible sensors as wearable electronic systems have attracted considerable attention for mimicking human skin to sense ambient stimuli.However,sensors need to have high resolution,stability and sensit...Multifunctional flexible sensors as wearable electronic systems have attracted considerable attention for mimicking human skin to sense ambient stimuli.However,sensors need to have high resolution,stability and sensitivity to realize fully biomimetic skin.Here,an assembled and welded Ag/W composite nanowire flexible electrode was prepared for body motion monitoring and flexible heaters.This Ag/W composite nanowire flexible electrode has a high transmittance of 90.1%(at 121Ω·sq^(−1) sheet resistance)and a low sheet resistance of 27Ω·sq^(−1)(at 60.1%transmittance).Although the transparency of this electrode is not high,the fluctuation in relative resistance change rate at 10%strain is only 5%after 1000 tensile cycles.It can be employed to monitor human body motions,including bending of fingers,arms,wrists,and throat action.Meanwhile,the Ag/W nanowires composite film heater achieves a steady-state temperature of up to 100℃ at a constant voltage of 3.5 V and an instantaneous heating rate of up to 36.5℃·s^(−1).展开更多
基金supported by the Beijing Natural Science Foundation(Grant No.L223013)。
文摘For the diagnostics and health management of lithium-ion batteries,numerous models have been developed to understand their degradation characteristics.These models typically fall into two categories:data-driven models and physical models,each offering unique advantages but also facing limitations.Physics-informed neural networks(PINNs)provide a robust framework to integrate data-driven models with physical principles,ensuring consistency with underlying physics while enabling generalization across diverse operational conditions.This study introduces a PINN-based approach to reconstruct open circuit voltage(OCV)curves and estimate key ageing parameters at both the cell and electrode levels.These parameters include available capacity,electrode capacities,and lithium inventory capacity.The proposed method integrates OCV reconstruction models as functional components into convolutional neural networks(CNNs)and is validated using a public dataset.The results reveal that the estimated ageing parameters closely align with those obtained through offline OCV tests,with errors in reconstructed OCV curves remaining within 15 mV.This demonstrates the ability of the method to deliver fast and accurate degradation diagnostics at the electrode level,advancing the potential for precise and efficient battery health management.
基金support from the National Natural Science Foundation of China(No’s.U22B2071,51874211,52031008)the Chilwee Group(CWDY-ZH-YJY-202101-001).
文摘Sodium(Na)and magnesium(Mg)are becoming important for making energy-storage batteries and structural materials.Herein,we develop a liquid-metal-electrode-assisted electrolysis route to producing Na and Mg with low-carbon emissions and no chlorine gas evolution.The clean production stems from the choice of a molten NaCl-Na_(2)CO_(3) electrolyte to prevent chlorine gas evolution,an inert nickel-based anode to produce oxygen,and a liquid metal cathode to make the cathodic product sit at the bottom of the electrolytic cell.We achieve a current efficiency of>90%for the electrolytic production of liquid Na-Sn alloy.Later,Mg-Sn alloy is prepared using the obtained Na-Sn alloy to displace Mg from molten NaCl-MgCl_(2) with a displacement efficiency of>96%.Further,Na and Mg are separated from the electrolytic Na-Sn and displaced Mg-Sn alloys by vacuum distillation with a recovery rate of>92%and Sn can be reused.Using this electrolysisdisplacement-distillation(EDD)approach,we prepare Mg from seawater.The CO_(2)emission of the EDD approach is~20.6 kg CO_(2)per kg Mg,which is less than that of the Australian Magnesium(AM)electrolysis process(~25.0 kg CO_(2)per kg Mg)and less than half that of the Pidgeon process(~45.2 kg CO_(2)per kg Mg).
基金funded by the Joint Fund for Regional Innovation and Development of National Natural Science Foundation of China(U21A20143)the National Science Fund for Excellent Young Scholars(52322607)the Excellent Youth Foundation of Heilongjiang Scientific Committee(YQ2022E028)。
文摘Improving the volumetric energy density of supercapacitors is essential for practical applications,which highly relies on the dense storage of ions in carbon-based electrodes.The functional units of carbon-based electrode exhibit multi-scale structural characteristics including macroscopic electrode morphologies,mesoscopic microcrystals and pores,and microscopic defects and dopants in the carbon basal plane.Therefore,the ordered combination of multi-scale structures of carbon electrode is crucial for achieving dense energy storage and high volumetric performance by leveraging the functions of various scale structu re.Considering that previous reviews have focused more on the discussion of specific scale structu re of carbon electrodes,this review takes a multi-scale perspective in which recent progresses regarding the structureperformance relationship,underlying mechanism and directional design of carbon-based multi-scale structures including carbon morphology,pore structure,carbon basal plane micro-environment and electrode technology on dense energy storage and volumetric property of supercapacitors are systematically discussed.We analyzed in detail the effects of the morphology,pore,and micro-environment of carbon electrode materials on ion dense storage,summarized the specific effects of different scale structures on volumetric property and recent research progress,and proposed the mutual influence and trade-off relationship between various scale structures.In addition,the challenges and outlooks for improving the dense storage and volumetric performance of carbon-based supercapacitors are analyzed,which can provide feasible technical reference and guidance for the design and manufacture of dense carbon-based electrode materials.
基金National Key R&D Program of China,Grant/Award Number:2023YFB2503900National Natural Science Foundation of China,Grant/Award Number:12172143Shenzhen Science and Technology Program,Grant/Award Numbers:JCYJ20220818100418040,JCYJ20220530160816038。
文摘Constructing silicon(Si)-based composite electrodes that possess high energy density,long cycle life,and fast charging capability simultaneously is critical for the development of high performance lithium-ion batteries for mitigating range anxiety and slow charging issues in new energy vehicles.Herein,a thick silicon/carbon composite electrode with vertically aligned channels in the thickness direction(VC-SC)is constructed by employing a bubble formation method.Both experimental characterizations and theoretical simulations confirm that the obtained vertical channel structure can effectively address the problem of sluggish ion transport caused by high tortuosity in conventional thick electrodes,conspicuously enhance reaction kinetics,reduce polarization and side reactions,mitigate stress,increase the utilization of active materials,and promote cycling stability of the thick electrode.Consequently,when paired with LiNi_(0.6)Co_(0.2)Mn_(0.2)O_(2)(NCM622),the VC-SC||NCM622 pouch type full cell(~6.0 mAh cm^(-2))exhibits significantly improved rate performance and capacity retention compared with the SC||NCM622 full cell with the conventional silicon/carbon composite electrode without channels(SC)as the anode.The assembled VC-SC||NCM622 pouch full cell with a high energy density of 490.3 Wh kg^(-1)also reveals a remarkable fast charging capability at a high current density of 2.0 mA cm^(-2),with a capacity retention of 72.0%after 500 cycles.
文摘Introduction The generation of biological wastes such as cow dung and aloe vera waste(AVW)causes a serious ecological pollution.The microbial electrolytic cell coupled with anaerobic digestion(MEC-AD)system can make a rational utilization of these biodegradable organic wastes,which is of vital importance for alleviating environmental deterioration and reducing resource waste.Electrode materials and accelerants are the two major factors that affect methane production in the MEC-AD system.They affect microbial attachment and electron transfer in the MEC-AD system.Bio-based carbon materials are carbon materials prepared from biomass as raw materials.They have characteristics such as a rich pore structure,good chemical stability,biocompatibility,and controllable surface properties,which can be used as accelerants and electrodes in the MEC-AD system to optimize its performance.This study was to investigate the influence of biomass-derived carbon as an electrode and accelerant on the performance of the MEC-AD system,and the mechanism for increasing the production of biogas and methane was also analyzed,thus providing a basis for the multifunctional application of biomass-derived carbon in the MEC-AD system.Methods A series of experimental methods were adopted to study the MEC-AD system.Two types of bio-based carbon,i.e.,aloe vera waste derived spherical carbon(AVW-SC)and porous carbon(AVW-PC),were synthesized via hydrothermal carbonization.The raw AVW material was washed with water,dried,ground,and subjected to hydrothermal treatment to obtain AVW-SC.After activating AVW-SC with KOH,it was carbonized in a tube furnace to obtain AVW-PC.In the preparation of the electrodes,bio-based carbon(AVW-SC and AVW-PC)was mixed with 5%polytetrafluoroethylene powder in ethanol and deionized water,and then ground in a ball mill for 4 h to form a slurry.The slurry was evenly sprayed on the Ti mesh,dried and sintered in N2 atmosphere at 360℃to obtain Ti-SC and Ti-PC electrodes.Four groups of experiments were conducted to determine the optimal voltage,compare different carbon electrodes,and explore the optimal coating amount.The MEC-AD reactor adopted 500 mL wide-mouthed glass bottles with a working volume of 400 mL.Each MEC-AD system received a co-substrate mixture of cattle dung and aloe vera waste and inoculum of sewage sludge in a mass ratio of 3:7.Afterward,they were placed at(36±1)℃for 35 d.The biogas was collected by a water displacement method.The materials were analyzed by characterization techniques such as X-ray diffraction(XRD)and scanning electron microscopy(SEM),and electrochemical tests were conducted on different electrodes.The composition,pH,TS,VS,TCOD and nutrient content of biogas were analyzed by standard chemical methods.Microbial community analysis was conducted using high-throughput sequencing technology.The modified Gompertz model was adopted to predict the kinetic parameters,and the coulombic efficiency and methane recovery rate were calculated according to a specific formula.Results and discussion The result shows that AVW-SC is spherical and closely aggregated,while AVW-PC has a three-dimensional network structure,with average pore diameter of 9.77 nm.The electron exchange capacity(EEC)of AVW-PC(i.e.,0.75μmol·e-/g)is higher than that of AVW-SC(i.e.,0.15μmol·e-/g),indicating a better electron exchange capacity.These results indicate that AVW-PC provides more substrate and bacteria accumulation sites,and has better electron-donating and electron-accepting ability,thus improving the digestion efficiency.In the MEC-AD system,using Ti mesh as an electrode,the effect of different voltages(i.e.,0,0.4,0.6,0.8 V and 1.2 V)on the system performance is investigated,obtaining the optimum biogas production and organic matter degradation rate at 0.8 V.AVW-SC and AVW-PC are respectively coated on Ti mesh as electrodes.The results show that the MEC-AD system with AVW-PC coated Ti mesh as the electrode has a better performance.The electrochemical analysis shows that the electrode coated with AVW-PC has a larger specific capacitance and a smaller charge transfer resistance,indicating that AVW-PC can improve the electrochemical properties and electron transfer ability of MEC-AD system.The influence of coating amount(i.e.,0.025,0.05,0.10,0.15,and 0.20 g)of AVW-PC on the MEC-AD system is investigated.At a coating amount of AVW-PC of 0.1 g,the cumulative biogas production and methane content of the Ti_(0.8)-PC_90.1) group both reach the maximum values.Different doses of AVW-PC(i.e.,0.10%,0.15%,0.20%,and 0.25%)are added as accelerants in Ti_(0.8)-PC_90.1).At the addition amount of AVW-PC of 0.20%,the Ti_(0.8)-PC_90.1)/PC0.2 group performs the optimum biogas production(i.e.,633.63 mL/g VS),methane content(i.e.,65.85%),and total nutrient content of biogas residue(i.e.,42.30 g/kg).In Ti_(0.8)-PC_90.1)/PC0.2,Bacteroidales,Pseudomonadales,Oscillospirales,Methanobacteraceae,Methanospirillaceae,Methanosarcinacea and Methanosaetaceae significantly increase.The increase in microbial diversity promotes interspecific hydrogen transfer(IHT),interspecific acetic transfer(IAT),and direct interspecific electron transfer(DIET),thereby enhancing methanogenic efficiency.Conclusions AVW-SC and AVW-PC were utilized as electrodes and accelerants to enhance methane yield in MEC-AD system.The Ti mesh electrode coated with different concentrations of AVW-PC achieved the optimal biogas production at 0.8 V.Specifically,the Ti_(0.8)-PC_90.1) combination could generate the maximum total amount of biogas and methane proportion.The Ti_(0.8)-PC_90.1)/PC0.2 combination exhibited the optimum performance(i.e.,biogas yield of 633.63 mL/g VS,methane content of 65.85%and total nutritional content of 42.30 g/kg).High abundances of Bacteroidales,Pseudomonadales,Oscillospirales,Methanobacteraceae,Methanospirillaceae,Methanosarcinaceae,and Methanosaetaceae appeared in the Ti_(0.8)-PC_90.1)/PC0.2 group,compared to other groups.In addition,an increased microbial diversity led to an enhanced methane production through processes like DIET.This research could highlight the potential significance of AVW-PC as both electrode and accelerator for increasing methane production and provide a perspective for improving MEC-AD performance through multiple applications of biomass-derived carbon.
基金supported by the Fundamental Research Funds for the Central Universities(WK2090000055)Anhui Provincial Natural Science Foundation of China(2308085QG231).
文摘As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation and fragmentation.This ultimately leads to a decrease in cell capacity.The trends of volume expansion and capacity change of the SiO/graphite(SiO/C)composite electrode during cycling were investigated via in situ expansion monitoring.First,a series of expansion test schemes were designed,and the linear relationship between negative electrode expansion and cell capacity degradation was quantitatively analyzed.Then,the effects of different initial pressures on the long-term cycling performance of the cell were evaluated.Finally,the mechanism of their effects was analyzed by scanning electron microscope.The results show that after 50 cycles,the cell capacity decreases from 2.556 mAh to 1.689 mAh,with a capacity retention ratio(CRR)of only 66.08%.A linear relationship between the capacity retention ratio and thickness expansion was found.Electrochemical measurements and scanning electron microscope images demonstrate that intense stress inhibits the lithiation of the negative electrode and that the electrode is more susceptible to irreversible damage during cycling.Overall,these results reveal the relationship between the cycling performance of SiO and the internal pressure of the electrode from a macroscopic point of view,which provides some reference for the application of SiO/C composite electrodes in lithium-ion batteries.
基金supported by the Materials/Parts Technology Development Programs(RS-2024-00466920,RS-2024-00432627,and RS-2024-00421058)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea).
文摘Rapid developments in lithium-ion battery(LIB)technology have been fueled by the expanding market for electric vehicles and increased demands for energy storage.Recently,thick electrode fabrication by solvent-free methods has emerged as a promising strategy for enhancing the energy density of LIBs.However,as electrode thickness increases,the tortuosity of lithium-ion transport also increases,resulting in severe polarization and poor electrochemical performance.Here,we investigate the effect of conductive agent morphology on the structural and electrochemical properties of 250μm thick lithium iron phosphate(LFP)/conductive agent/polytetrafluoroethylene(PTFE)-based electrodes.Three commercially available conductive additives,namely 0D Super P,1D multi-walled carbon nanotubes(MWCNTs),and 2D graphene nanoplatelets(GNPs),were incorporated into LFP-based electrodes.The MWCNT-incorporated electrode with a high loading mass(42 mg cm^(-2))exhibited a high porosity(ε=51%)and low tortuosity(τ=4.02)owing to its highly interconnected fibrous network of MWCNTs.Due to the fast lithium-ion transport kinetics in the MWCNT-incorporated electrode,the electrochemical performances exhibited a high specific capacity of 157 mAh g^(-1)at 0.1 C and an areal capacity of 7.16 mAh cm^(-2)at 0.1 C with a high-rate capability and excellent cycling stability over 300 cycles at 0.1 C.This study provides a guidance for utilizing conductive agents to apply in the low tortuous thick electrode fabricated by a solvent-free process.Additionally,this work paves the way to achieve scalable and sustainable dry processing techniques for developing next-generation energy storage technologies.
基金supported by the National Natural Science Foundation of China(Nos.62374035,92263106,12061131009)the Science and Technology Commission of Shanghai Municipality(No.21520712600).
文摘Silver nanowires(Ag NWs)have promising application potential in electronic displays because of their superior flexibility and transparency.Doping Ni in Ag NWs has proven to be an effective strategy to im-prove its work function.However,AgNi NWs-based electrodes suffer from poor electrical conductivity under air exposure due to the low-conductivity NiO generated on its surface.Here,Cu was further doped in AgNi NWs to form AgNiCu NWs and regulate its surface oxide under long-term air exposure.Finally,it is demonstrated that the conductivity of AgNiCu NWs can acquire an improved tolerable tempera-ture(over 240℃)and prolonged high-temperature tolerance time(over 150 min)by finely regulating the doping content Cu,indicating an enhanced air-stable conductivity.The optimized AgNiCu NWs also achieve superior transparent conductivity as pure Ag NWs and high work function as AgNi NWs,which has been successfully applied in constructing an n-type photodiode with an effective rectification effect.
基金supported by the Institute of Civil Military Technology Cooperation funded by the Defense Acquisition Program Administration and Ministry of Trade,Industry and Energy of Korean government under grant No 23-CM-AI-08.
文摘Amidst the ever-growing interest in high-mass-loading Li battery electrodes,a persistent challenge has been the insufficient continuity of their ion/electron conduction pathways.Here,we propose cellulose elementary fibrils(CEFs)as a class of deagglomerated binder for high-mass-loading electrodes.Derived from natural wood,CEF represents the most fundamental unit of cellulose with nanoscale diameter.The preparation of the CEFs involves the modulation of intermolecular hydrogen bonding by the treatment with a proton acceptor and a hydrotropic agent.This elementary deagglomeration of the cellulose fibers increases surface area and anionic charge density,thus promoting uniform dispersion with carbon conductive additives and suppressing interfacial side reactions at electrodes.Consequently,a homogeneous redox reaction is achieved throughout the electrodes.The resulting CEF-based cathode(overlithiated layered oxide(OLO)is chosen as a benchmark electrode active material)exhibits a high areal-mass-loading(50 mg cm^(-2),equivalent to an areal capacity of 12.5 mAh cm^(-2))and a high specific energy density(445.4 Wh kg–1)of a cell,which far exceeds those of previously reported OLO cathodes.This study highlights the viability of the deagglomerated binder in enabling sustainable high-mass-loading electrodes that are difficult to achieve with conventional synthetic polymer binders.
基金supported by the National Natural Science Foundation of China(No.22271101)the R&D Program of Guangzhou(2024A04J2497)+1 种基金the Key Laboratory of Polymer Chemistry&Physics of Ministry of Educationsupported by the High Performance Computing Platform of SCUT。
文摘High-entropy oxides(HEOs),offering reversible lithium storage and moderate operating potential,are considered promising negative electrodes.However,the intricate lithium storage mechanism within HE polycationic systems remains challenging.Here,we conduct comprehensive investigations into the electrochemical properties and structu ral evolution of(CrMnCoNiZn)_(3)O_(4)(HESO)to clarify lithium storage mechanisms.Density functional theory(DFT)calculations reveal that polycationic synergy modulates the electronic structure and d-band centers of HESO,delivering fast electrode kinetics.Exhaustive in-and exsitu analyses demonstrate that the residual crystalline phases acting as seed crystals maintain the spinel/rock-salt lattice persistence under the entropy stabilization effect,lattice distortion effect,and cation synergy,which guide cation crystallization upon the electric field to drive reversible lithium storage.Such properties underlie the HESO electrode with an exceptional rate and long-term capability.This work clarifies the roles of cationic synergy and seed-crystal-driven structural reversibility,providing a blueprint for designing high-performance HEO negative electrodes for next-generation lithium-ion batteries(LIBs).
基金the National Natural Science Foundation of China(Nos.21706153,52270078)Natural Science Basic Research Program of Shaanxi Province(Nos.2018JQ2066,2022JM065)。
文摘Boron-doped diamond(BDD)is a well-known anode material with a high pollutant degradation ability for electrochemical oxidation wastewater treatment.Nevertheless,the cost of production and mechanical strength of BDD membranes remain unsatisfactory.Magnetic BDD particles derived from industrial waste may represent a promising alternative to BDD membranes,although the challenge remains in assembling these particles into a usable electrode.In this study,magnetic BDD particles were attracted to a Ti/RuO_(2)-IrO_(2)electrode using a magnet,thus constituting a novel 2.5-dimensional(2.5D)electrode.To ascertain the structure-activity relationship of the novel electrode,essential characterizations,multi-physics simulations,pollutant degradation and electrosynthesis experiments were conducted.The results indicate that an appropriate quantity of BDD particles(0.1 g/cm^(2))can enhance the number of active sites by approximately 20%.A strong synergistic effect was observed between the Ti/Ti/RuO_(2)-IrO_(2)and BDD particles in the degradation of various pollutants,including azo dye,p-benzoquinone,succinic acid and four kinds of real wastewaters,as well as glycerol conversion.The joint active sites on the interface between Ti/RuO_(2)-IrO_(2)and BDD particles,as well as the inner active sites on BDD particles,have been identified as crucial in the mineralization of pollutants and the generation of value-added products.The optimal amount of BDD particles(0.1 g/cm^(2))is sufficient to preserve the joint active sites and to maintain an adequate polarization on the BDD particles.Nevertheless,the hybrid feature of the 2.5D electrode is diminished when a greater quantity of BDD particles(0.3 g/cm^(2))is loaded.
基金supported by the National Natural Science Foundation of China(Grant Nos.22378342,92372101,52162036,and 21875155)the Fundamental Research Funds for the Central Universities(20720220010)+3 种基金the National Key Research and Development Program of China(2021YFA1201502)the Natural Science Foundation of Sichuan Province(Grant No.2024NSFSC1160)the Postdoctoral Fellowship Program of CPSF(Grant No.GZB20230608)support of Nanqiang Young Top-notch Talent Fellowship in Xiamen University。
文摘Silicon monoxide(SiO)is highly attractive as an anode material for high-energy lithium-ion batteries(LIBs)due to its significantly higher specific capacity.However,its practical application is hindered by substantial volume expansion during cycling,which leads to material pulverization and an unstable solid electrolyte interphase(SEI)layer.Inspired by the natural root fixation in soil,we designed a root-like topological structure binder,cassava starch-citric acid(CS-CA),based on the synergistic action of covalent and hydrogen bonds.The abundant-OH and-COOH groups in CS-CA molecules effectively form hydrogen bonds with the-OH groups on the SiO surface,significantly enhancing the interfacial interaction between CS-CA and SiO.The root-like topological structure of CS-CA with a high tolerance alleviates the mechanical stress generated by the volume changes of SiO.More encouragingly,the hydrogen bond action among CS-CA molecules produces a self-healing effect,which is advantageous for repairing damaged electrodes and preserving their structural integrity.As such,the CS-CA/SiO electrode exhibits exceptional cycling performance(963.1 mA h g^(-1)after 400 cycles at 2 A g^(-1))and rate capability(558.9 mA h g^(-1)at 5 A g^(-1)).This innovative,topologically interconnected,root-inspired binder will greatly advance the practical application of long-lasting micron-sized SiO anodes.
基金financially supported by the Guangdong Basic and Applied Basic Research Foundation(Nos.2022B1515020001,2024A1515010277)the National Natural Science Foundation of China(Nos.22109052,52202221)+1 种基金Guangzhou Science and Technology Program(No.2024A04J3899)the Fundamental Research Funds for the Central Universities(No.21624410)。
文摘Benefiting from the low cost and high abundance of potassium resources,K-based batteries have attracted numerous research interest as a more sustainable battery chemist,particularly when considering the enormous demand for sustainable energy storage while limiting Li sources for Li-based batteries.However,the much larger size of the K-ion usually leads to the serious electrodes'volumetric expansion with rapid capacity fading,making the pursuit of electrodes for potassium storage with high capacity and high stability a significant challenge.The polymer electrode materials have been considered promising materials to address these issues due to their porous characteristics,insolubility in electrolytes,and flexible structural design at a molecular level.In this review,we outline the recent advancements in redox-active polymer electrodes,including anode and cathode,materials for K-based batteries,including crystalline porous coordination polymers,crystalline covalent organic polymers,amorphous polymers,and polymer composites.We discuss the electrode designs,electrochemical performances,and K-ion storage mechanism,with a focus on their structure-function correlations.With this knowledge,we propose the perspectives and challenges in designing advanced polymer electrode materials for K-based batteries.We expect this review will shed light on the further development of reliable polymer electrode materials.
基金supported by the National Natural Science Foundation of China(No.U2037601)the National Key Research and Development Program(No.2023YFB3809500)the Chongqing Technology Innovation and Application Development Project(No.CSTB2022TIAD-KPX0028).
文摘Rechargeable magnesium batteries(RMBs)have attracted much attention due to the high theoretical capacity(3833 mAh cm−3)of magnesium metal negative electrode and abundant resources.However,the preparation of ultra-thin magnesium foils faces the problems of rolling difficulty and high processing cost,while the use of thick magnesium foils leads to low utilization of magnesium and reduces the energy density.To tackle the above problems,we successfully prepared ultra-thin magnesium foils based on electrolytic process and investigated the effect of different substrates.The magnesium foils prepared using Mo substrate have more uniform surface morphology and lower surface roughness,which is attributed to the lower magnesium nucleation overpotential of Mo substrate.Meanwhile,density functional theory calculations show that the adsorption energy of Mo on Mg is more negative,which is conducive to achieving uniform nucleation and deposition of Mg.The Mg deposition on Mo substrate undergoes the characteristic stages of transient nucleation,nucleus accretion,multidirectional heterotopic growth,and columnar crystal stacking,and ultimately the formation of a dense deposited layer.In addition,the prepared ultra-thin Mg foil with Mo substrate can stably cycle for 1000 h at 3 mA cm^(-2) with high utilization of 50% in the symmetric cell.This study develops a facile method for the preparation of ultra-thin Mg foils,which opens up a new path for developing high-performance ultra-thin negative electrodes for RMBs.
基金supported by the National Key R&D Program of China(No.2023YFB4004700)。
文摘Anion exchange membrane fuel cells(AEMFCs)are considered a more affordable technology compared to proton exchange membrane fuel cells(PEMFCs),but the performance and durability of AEMFCs are still not competent with PEMFCs owing to the more challenging water management,which severely hinders its development and real-life applications.In this study,we introduce the strategy to boost the performance and stability of the membrane electrode assembly(MEA)of AEMFCs by regulating the hydrophilicity of the anode and cathode ionomers.Two poly(biphenyl alkylene)ionomers with different hydrophilicity are synthesized and used to fabricate MEAs with asymmetric or symmetric ionomer configurations in the anodic and cathodic catalyst layers(CLs)for AEMFCs.Molecular dynamics(MD)simulations have revealed different diffusion rates of water in the hydrophobic anode and the hydrophilic cathode,which show the potential of this design to improve water management in AEMFCs,The effectiveness of this design is also confirmed by experimental results that the MEA with this asymmetric configuration exhibits the highest power and current densities of 1.58 W cm^(-2)or 5.58 A cm^(-2),respectively,among all configurations.Furthermore,this configuration also enhances the durability,with the MEA showing a voltage decay rate of only 313.1μV h^(-1)after 500 h of in-situ durability test at 0.2 A cm^(-2).This study provides new insights into the rational design of more efficient water management in MEA for high-performance AEMFCs.
基金supported by the National Natural Science Foundation of China(Nos.51905103,52275177).
文摘Multifunctional flexible sensors as wearable electronic systems have attracted considerable attention for mimicking human skin to sense ambient stimuli.However,sensors need to have high resolution,stability and sensitivity to realize fully biomimetic skin.Here,an assembled and welded Ag/W composite nanowire flexible electrode was prepared for body motion monitoring and flexible heaters.This Ag/W composite nanowire flexible electrode has a high transmittance of 90.1%(at 121Ω·sq^(−1) sheet resistance)and a low sheet resistance of 27Ω·sq^(−1)(at 60.1%transmittance).Although the transparency of this electrode is not high,the fluctuation in relative resistance change rate at 10%strain is only 5%after 1000 tensile cycles.It can be employed to monitor human body motions,including bending of fingers,arms,wrists,and throat action.Meanwhile,the Ag/W nanowires composite film heater achieves a steady-state temperature of up to 100℃ at a constant voltage of 3.5 V and an instantaneous heating rate of up to 36.5℃·s^(−1).
