The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties o...The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties of various glycol dimethyl ethers are screened,and diglyme(G2)is selected as the sole solvent for the electrolyte.Lithium bis(fluorosulfonyl)imide(LiFSI),a highly dissociative salt,is used as the primary salt;while lithium nitrate(LiNO_(3))and lithium difluorophosphate(LiDFP),which have small ionic sizes and strong binding energies,are added as secondary salts.The resulting electrolyte can modulate the electric double layer structure by NO_(3)^(-) and DFP^(-) on the cathode side,leading to an increased Liþconcentration that is originally repelled by the cathode.Additionally,the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable,thereby enhancing the electrochemical performance of the cells.As a result,cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 V.The LijjNCM811 cells maintain 80.2%capacity retention after 270 cycles at room temperature,with an average Coulombic efficiency of 99.5%,and exhibit 88.4%capacity retention after 200 cycles at -30℃.展开更多
The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vi...The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vital role of noble metals in electrocatalytic activity,this work focuses on the rational synthesis of Ni-noble metal composite nanocatalysts for overcoming the drawbacks of high cost and susceptible oxidized surfaces of noble metals.The inherent catalytic activity is improved by the altered electronic structure and effective active sites of the catalyst induced by the size effect of noble metal clusters.In particular,a series of Ni-noble metal nanocomposites are successfully synthesized by partially introducing noble metal into Ni with porous interfacial defects derived from Ni-Al layered double hydroxide(LDH).The Ni_(10)Pd_(1)nanocomposite exhibits high OER catalytic activity with an overpotential of 0.279 V at 10 m A/cm^(2),surpassing Ni_(10)Ag_(1)and Ni_(10)Au_(1)counterparts.Furthermore,the average diameter of Pd clusters gradually increases from 5.57 nm to 44.44 nm with the increased proportion of doped Pd,leading to the passivation of catalytic activity due to the exacerbated surface oxidation of Pd in the form of Pd^(2+).After optimization,Ni_(10)Pd_(1)delivers significantly enhanced OER and MOR electroactivities and long-term stability compared to that of Ni_(2)Pd_(1),Ni_(1)Pd_(1)and Ni_(1)Pd_(2),which is conducive to the effective utilization of Pd and alleviation of surface oxidation.展开更多
During restorative dental procedures,complete control over the operative site is critical for patient comfort,safety,and the operator’s access and visibility.The success of a fixed prosthesis depends on accurate impr...During restorative dental procedures,complete control over the operative site is critical for patient comfort,safety,and the operator’s access and visibility.The success of a fixed prosthesis depends on accurate impression making of the prepared finish lines on the abutment teeth.To optimise long-term outcomes for the fixed restoration,gingival retraction techniques should be used to decrease the marginal discrepancy among the restoration and the prepared abutment.Accurate marginal positioning of the restoration along the prepared finish line of the abutment is essential for therapeutic,preventive,and aesthetic purposes.展开更多
Rechargeable magnesium batteries(RMBs)are a cutting-edge energy storage solution,with several advantages over the state-of-art lithiumion batteries(LIBs).The use of magnesium(Mg)metal as an anode material provides a m...Rechargeable magnesium batteries(RMBs)are a cutting-edge energy storage solution,with several advantages over the state-of-art lithiumion batteries(LIBs).The use of magnesium(Mg)metal as an anode material provides a much higher gravimetric capacity compared to graphite,which is currently used as the anode material in LIBs.Despite the significant advances in electrolyte,the development of cathode material is limited to materials that operate at low average discharge voltage(<1.0 V vs.Mg/Mg^(2+)),and developing high voltage cathodes remains challenging.Only a few materials have been shown to intercalate Mg^(2+)ions reversibly at high voltage.This review focuses on the structural aspects of cathode material that can operate at high voltage,including the Mg^(2+)intercalation mechanism in relation to its electrochemical properties.The materials are categorized into transition metal oxides and polyanions and subcategorized by the intrinsic Mg^(2+)diffusion path.This review also provides insights into the future development of each material,aiming to stimulate and guide researchers working in this field towards further advancements in high voltage cathodes.展开更多
This review focuses on the significant impact of heteroatom doping in enhancing the electronic properties and electrochemical performance of carbon materials for supercapacitors(SCs).Incorporating heteroatoms such as ...This review focuses on the significant impact of heteroatom doping in enhancing the electronic properties and electrochemical performance of carbon materials for supercapacitors(SCs).Incorporating heteroatoms such as nitrogen,sulfur,phosphorus,fluorine,and boron modifies the carbon structure,creates defects and increases active sites,which improves electronic conductivity,ion accessibility,and surface wettability and reduces ion diffusion barriers.Additionally,certain heteroatoms can participate in electrochemical reactions,further enhancing SC performance.Although research in this area is still emerging,a deeper understanding of the mechanisms behind single and multi-doping systems is essential for developing next-generation materials.Future strategies for improving heteroatom-doped carbon materials include increasing heteroatom content to enhance specific capacitance,selecting suitable heteroatoms to expand the potential window and improve energy density,utilizing advanced in situ characterization techniques,and exploring the use of these materials in cost-effective SCs.The potential of heteroatom-doped carbon materials for SCs is promising,with their ability to improve energy density,power density,and cycling stability,making them competitive with other energy storage technologies.These advancements will be key to broadening their practical applications,including electric vehicles,portable electronics,and grid energy storage,and will contribute to more efficient,long-lasting,and environmentally friendly energy storage solutions.展开更多
Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising ph...Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising photocatalysts for H_(2)O_(2)production due to their unique electronic,optical properties,and tunable structures.However,the high exciton binding energy of CPs hinders efficient exciton dissociation and charge separation,limiting their photocatalytic performance.In this work,we synthesized scandium(Sc)atoms decorated CPs with enhanced ordered stacking and crystallinity by introducing benzaldehyde as an end-capping reagent.The strong interaction between charged Sc atoms and electrons facilitates exciton dissociation and improves charge transfer capability.Furthermore,the Lewis acidic nature of Sc atoms promotes oxygen adsorption and enhances the stabilization of superoxide anion intermediate(·O_(2)^(-)).As a result,the as-synthesized photocatalysts exhibit a high H_(2)O_(2)production rate of 18μmol h^(-1)in pure water,which is three times that of pristine CPs,This work provides valuable insights into the design of organic polymer photocatalysts for various photocatalytic reactions.展开更多
Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal s...Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal sites in 3D COFs predominantly exhibit symmetrical coordination,making them unsuitable for CO_(2)activation.Here,we design a 3D COF with 2,2'-pyridine linked around tetra-(4-anilyl)methane(TCM-Bpy-COF),where Co^(2+)is asymmetrically coordinated by bipyridine and acetates(TCMBpy-COF-CoAc).The TCM-Bpy-COF-CoAc exhibits outstanding photocatalytic CO_(2)reduction performance under weak visible light,achieving a CO evolution rate of 26,650μmol g^(-1)h^(-1)under 5 W of lightemitting-diode(LED)lamp and high apparent quantum efficiency.The performance far exceeds that of symmetrically coordinated bipyridine-Co-bipyridine TCM-Bpy-COF and surpasses most reported COF-based photocatalysts.In-situ spectral characterizations and theoretical calculations show that asymmetric N,O-coordination around the Co^(2+)center polarizes electron density and lowers reaction energy barriers of^(*)COOH intermediates,enhancing the conversion of CO_(2)to CO.This work inspires the design of 3D COF-based photocatalysts with highly catalytic efficiency.展开更多
Methane chemistry is one of the“Holy Grails of catalysis”.It is highly desirable but challenge to transform methane into value-added chemicals,because of its high C-H bonding energy(435 kJ/mol),lack ofπbonding or u...Methane chemistry is one of the“Holy Grails of catalysis”.It is highly desirable but challenge to transform methane into value-added chemicals,because of its high C-H bonding energy(435 kJ/mol),lack ofπbonding or unpaired electrons.Currently,commercial methane conversion is usually carried out in harsh conditions with enormous energy input.Photocatalytic partial oxidation of methane to liquid oxygenates(PPOMO)is a future-oriented technology towards realizing high efficiency and high selectivity under mild conditions.The selection of oxidant is crucial to the PPOMO performance.Hence,attentions are paid to the research progress of PPOMO with various oxidants(O_(2),H_(2)O,H_(2)O_(2)and other oxidants).Moreover,the activation of the selected oxidants is also highly emphasized.Meanwhile,we summarized the methane activation mechanisms focusing on the C-H bond that was broken mainly by·OH radical,O-specie or photogenerated hole(h+).Finally,the challenges and prospects in this subject are briefly discussed.展开更多
This study evaluated the simulation performance of mesoscale convective system(MCS)-induced precipitation,focusing on three selected cases that originated from the Yellow Sea and propagated toward the Korean Peninsula...This study evaluated the simulation performance of mesoscale convective system(MCS)-induced precipitation,focusing on three selected cases that originated from the Yellow Sea and propagated toward the Korean Peninsula.The evaluation was conducted for the European Centre for Medium-Range Weather Forecasts(ECMWF)and National Centers for Environmental Prediction(NCEP)analysis data,as well as the simulation result using them as initial and lateral boundary conditions for the Weather Research and Forecasting model.Particularly,temperature and humidity profiles from 3D dropsonde observations from the National Center for Meteorological Science of the Korea Meteorological Administration served as validation data.Results showed that the ECMWF analysis consistently had smaller errors compared to the NCEP analysis,which exhibited a cold and dry bias in the lower levels below 850 hPa.The model,in terms of the precipitation simulations,particularly for high-intensity precipitation over the Yellow Sea,demonstrated higher accuracy when applying ECMWF analysis data as the initial condition.This advantage also positively influenced the simulation of rainfall events on the Korean Peninsula by reasonably inducing convective-favorable thermodynamic features(i.e.,warm and humid lower-level atmosphere)over the Yellow Sea.In conclusion,this study provides specific information about two global analysis datasets and their impacts on MCS-induced heavy rainfall simulation by employing dropsonde observation data.Furthermore,it suggests the need to enhance the initial field for MCS-induced heavy rainfall simulation and the applicability of assimilating dropsonde data for this purpose in the future.展开更多
Molybdenum disulfide(MoS_(2))has garnered significant attention in the field of catalysis due to the high density of active sites in its unique two-dimensional(2D)structure,which could be developed into numerous high-...Molybdenum disulfide(MoS_(2))has garnered significant attention in the field of catalysis due to the high density of active sites in its unique two-dimensional(2D)structure,which could be developed into numerous high-performance catalysts.The synthesis of ultra-small MoS2 particles(<10 nm)is highly desired in various experimental studies.The ultra-small structure could often lead to a distinct S-Mo coordination state and nonstoichiometric composition in MoSx,minimizing in-plane active sites of the 2D structure and making it probable to regulate the atomic and electronic structure of its intrinsic active sites on a large extent,especially in MoSx clusters.This article summarizes the recent progress of catalysis over ultra-small undoped MoS_(2) particles for renewable fuel production.Through a systematic review of their synthesis,structural,and spectral characteristics,as well as the relationship between their catalytic performance and inherent defects,we aim to provide insights into catalysis over this matrix that may potentially enable advancement in the development of high-performance MoS_(2)-based catalysts for sustainable energy generation in the future.展开更多
Magnesium-ion batteries(MIBs)are promising candidates for lithium-ion batteries because of their abundance,non-toxicity,and favorable electrochemical properties.This review explores the reaction mechanisms and electro...Magnesium-ion batteries(MIBs)are promising candidates for lithium-ion batteries because of their abundance,non-toxicity,and favorable electrochemical properties.This review explores the reaction mechanisms and electrochemical characteristics of Mg-alloy anode materials.While Mg metal anodes provide high volumetric capacity and dendrite-free electrodeposition,their practical application is hindered by challenges such as sluggish Mg^(2+)ion diffusion and electrolyte compatibility.Alloy-type anodes that incorporate groups XIII,XIV,and XV elements have the potential to overcome these limitations.We review various Mg alloys,emphasizing their alloying/dealloying reaction mechanisms,their theoretical capacities,and the practical aspects of MIBs.Furthermore,we discuss the influence of the electrolyte composition on the reversibility and efficiency of these alloy anodes.Emphasis is placed on overcoming current limitations through innovative materials and structural engineering.This review concludes with perspectives on future research directions aimed at enhancing the performance and commercial viability of Mg alloy anodes and contributing to the development of high-capacity,safe,and cost-effective energy storage systems.展开更多
Dynamic transformation(DT)of austenite(γ)to ferrite(α)in the hot deformation of various carbon steels was widely investigated.However,the nature of DT remains unclear due to the lack of quantitative analysis of stre...Dynamic transformation(DT)of austenite(γ)to ferrite(α)in the hot deformation of various carbon steels was widely investigated.However,the nature of DT remains unclear due to the lack of quantitative analysis of stress partitioning between two phases and the uncertainty of local distribution of substitu-tional elements at the interface in multi-component carbon steels used in the previous studies.Therefore,in the present study,a binary Fe-Ni alloy withα+γduplex microstructure in equilibrium was prepared and isothermally compressed inα+γtwo-phase region to achieve a quantitative analysis of microstruc-ture evolution,stress partitioning,and thermodynamics during DT.γtoαDT during isothermal compres-sion andαtoγreverse transformation on isothermal annealing under unloaded condition after deforma-tion were accompanied by Ni partitioning.The lattice strains during thermomechanical processing were obtained via in-situ neutron diffraction measurement,based on which the stress partitioning behavior betweenγandαwas discussed by using the generalized Hooke’s law.A thermodynamic framework for the isothermal deformation in solids was established based on the basic laws of thermodynamics,and it was shown that the total Helmholtz free energy change in the deformable material during the isothermal process should be smaller than the work done to the deformable material.Under the present thermody-namic framework,the microstructure evolution in the isothermal compression of Fe-14Ni alloy was well explained by considering the changes in chemical free energy,plastic and elastic energies,and the work done to the material.In addition,the stabilization of the softαphase in Fe-14Ni alloy by deformation was rationalized since theγtoαtransformation decreased the total Helmholtz free energy by decreasing the elastic and dislocation energies.展开更多
The exploration of newer antibacterial strategies is driven by antibiotic‐resistant microbes that cause serious public health issues.In recent years,nanoscale materials have developed as an alternative method to figh...The exploration of newer antibacterial strategies is driven by antibiotic‐resistant microbes that cause serious public health issues.In recent years,nanoscale materials have developed as an alternative method to fight infections.Despite the fact that many nanomaterials have been discovered to be harmful,numerous researchers have shown a keen interest in nanoparticles(NPs)made of noble metals like silver,gold and platinum.To make environmentally safe NPs from plants,green chemistry and nanotechnology have been combined to address the issue of toxicity.The study of bimetallic nanoparticles(BNPs)has increased tremendously in the past 10 years.The production of BNPs mediated by natural extracts is straightforward,low cost and environmentally friendly.Due to their low toxicity,safety and biological stability,noble BNPs with silver,gold,platinum and palladium have the potential to be used in biomedical applications.They have a significant impact on human health and are used in medicine and pharmacy due to their biological characteristics,which include catalytic,antioxidant,antibacterial,antidiabetic,anticancer,hepatoprotective and regenerative activity.展开更多
The design of nanostructured materials occupies a privileged position in the development and management of affordable and effective technology in the antibacterial sector.Here,we discuss the antimicrobial properties o...The design of nanostructured materials occupies a privileged position in the development and management of affordable and effective technology in the antibacterial sector.Here,we discuss the antimicrobial properties of three carbonaceous nanoblades and nanodarts materials of graphene oxide(GO),reduced graphene oxide(RGO),and single-wall carbon nanotubes(SWCNTs)that have a mechano-bactericidal effect,and the ability to piercing or slicing bacterial membranes.To demonstrate the significance of size,morphology and composition on the antibacterial activity mechanism,the designed nanomaterials have been characterized.The minimum inhibitory concentration(MIC),standard agar well diffusion,and transmission electron microscopy were utilized to evaluate the antibacterial activity of GO,RGO,and SWCNTs.Based on the evidence obtained,the three carbonaceous materials exhibit activity against all microbial strains tested by completely encapsulating bacterial cells and causing morphological disruption by degrading the microbial cell membrane in the order of RGO>GO>SWCNTs.Because of the external cell wall structure and outer membrane proteins,the synthesized carbonaceous nanomaterials exhibited higher antibacterial activity against Gram-positive bacterial strains than Gram-negative and fungal microorganisms.RGO had the lowest MIC values(0.062,0.125,and 0.25 mg/mL against B.subtilis,S.aureus,and E.coli,respectively),as well as minimum fungal concentrations(0.5 mg/mL for both A.fumigatus and C.albicans).At 12 hr,the cell viability values against tested microbial strains were completely suppressed.Cell lysis and death occurred as a result of severe membrane damage caused by microorganisms perched on RGO nanoblades.Our work gives an insight into the design of effective graphene-based antimicrobial materials for water treatment and remediation.展开更多
Growing energy demand drives the rapid development of clean and reliable energy sources.In the past years,the exploration of novel materials with considerable efficiency and durability has drawn attention in the area ...Growing energy demand drives the rapid development of clean and reliable energy sources.In the past years,the exploration of novel materials with considerable efficiency and durability has drawn attention in the area of electrochemical energy conversion.Transition metal macrocyclic metallophthalocyanines(MPcs)-based catalysts with a peculiar 2D constitution have emerged with a promising future account of their highly structural tailorability and molecular functionality which greatly extend their functionalities as electrocatalytic materials for energy conversion.This review summarizes the systematic engineering of synthesis of MPcs and their analogs in detail,and mostly pays attention to the frontier research of MPc-based high-performance catalysts toward different electrocatalytic processes concerning hydrogen,oxygen,water,carbon dioxide,and nitrogen,with a particular focus on discussing the interrelationship between the electrocatalytic activity and component/structure,as well as functional applications of MPcs.Finally,we give the gaps that need to be addressed after much thought.展开更多
The development of superconducting joining technology for reacted magnesium diboride(MgB_(2))conductors remains a critical challenge for the advancement of cryogen-free MgB_(2)-based magnets for magnetic resonance ima...The development of superconducting joining technology for reacted magnesium diboride(MgB_(2))conductors remains a critical challenge for the advancement of cryogen-free MgB_(2)-based magnets for magnetic resonance imaging(MRI).Herein,the fabrication of superconducting joints using reacted carbon-doped multifilament MgB_(2)wires for MRI magnets is reported.To achieve successful superconducting joints,the powder-in-mold method was employed,which involved tuning the filament protection mechanism,the powder compaction pressure,and the heat treatment condition.The fabricated joints demonstrated clear superconducting-to-normal transitions in self-field,with effective magnetic field screening up to 0.5 T at 20 K.To evaluate the interface between one of the MgB_(2)filaments and the MgB_(2)bulk within the joint,serial sectioning was conducted for the first time in this type of superconducting joint.The serial sectioning revealed space formation at the interface,potentially caused by the volume shrinkage associated with the MgB_(2)formation or the combined effect of the volume shrinkage and the different thermal expansion coefficients of the MgB_(2)bulk,the filament,the mold,and the sealing material.These findings are expected to be pivotal in developing MgB_(2)superconducting joining technology for MRI magnet applications through interface engineering.展开更多
Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexi...Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexible cation(H_(2)imb)^(2+)((H_(2)imb)^(2+)=di-protonated 2,3-bis(imidazolin-2-yl)-2,3-dimethylbutane)has been developed.Electron-donating Cl−and(ZnCl4)2−are used to direct folding a flexible electron-deficient(H_(2)imb)^(2+)cation.Three complexes(H_(2)imb)(NO_(3))2(1),(H_(2)imb)Cl2·H_(2)O(2),and(H_(2)imb)ZnCl4(3)have been synthesized in which(H_(2)imb)^(2+)crystallize in an anti-conformation,88.8°-gauche,and 51.8°-gauche,respectively.In contrary to X-ray silent complex 1,X-ray induced photochromism has been achieved in both complex 2 and 3.An intermolecular charge-transfer mechanism has been elucidated and the anion directed folding of(H_(2)imb)^(2+)has been validated to be critical to yield colored long-lived charge-separated states.展开更多
A dye-sensitized photocatalyst combining Pt-loaded TiO_(2) and Ru(Ⅱ)tris-diimine sensitizer(RuP)was constructed and its activity for photochemical hydrogen evolution was compared with that of Pt-intercalated HCa_(2)N...A dye-sensitized photocatalyst combining Pt-loaded TiO_(2) and Ru(Ⅱ)tris-diimine sensitizer(RuP)was constructed and its activity for photochemical hydrogen evolution was compared with that of Pt-intercalated HCa_(2)Nb_(3)O_(10) nanosheets.When the sacrificial donor ethylenediaminetetraacetic acid(EDTA)disodium salt dihydrate was used,RuP/Pt/TiO_(2) showed higher activity than RuP/Pt/HCa_(2)Nb_(3)O_(10).In contrast,when NaI(a reversible electron donor)was used,RuP/Pt/TiO_(2) showed little activity due to back electron transfer to the electron acceptor(I_(3)-),which was gener-ated as the oxidation product of I-.By modification with anionic polymers(sodium poly(styrenesulfonate)or sodium polymethacrylate)that could inhibit the scavenging of conduction band electrons by I_(3)-,the H_(2) production activity from aqueous NaI was improved,but it did not exceed that of RuP/Pt/HCa_(2)Nb_(3)O_(10).Transient absorption measurements showed that the rate of semiconductor-to-dye back electron transfer was slower in the case of TiO_(2) than HCa_(2)Nb_(3)O_(10),but the electron transfer reaction to I3-was much faster.These results indicate that Pt/TiO_(2) is useful for reactions with sacrificial reductants(e.g.,EDTA),where the back electron transfer reaction to the more reducible product can be neglected.However,more careful design of the catalyst will be nec-essary when a reversible electron donor is employed.展开更多
The current global warming,coupled with the growing demand for energy in our daily lives,necessitates the development of more efficient and reliable energy storage devices.Lithium batteries(LBs)are at the forefront of...The current global warming,coupled with the growing demand for energy in our daily lives,necessitates the development of more efficient and reliable energy storage devices.Lithium batteries(LBs)are at the forefront of emerging power sources addressing these challenges.Recent studies have shown that integrating hexagonal boron nitride(h-BN)nanomaterials into LBs enhances the safety,longevity,and electrochemical performance of all LB components,including electrodes,electrolytes,and separators,thereby suggesting their potential value in advancing eco-friendly energy solutions.This review provides an overview of the most recent applications of h-BN nanomaterials in LBs.It begins with an informative introduction to h-BN nanomaterials and their relevant properties in the context of LB applications.Subsequently,it addresses the challenges posed by h-BN and discusses existing strategies to overcome these limitations,offering valuable insights into the potential of BN nanomaterials.The review then proceeds to outline the functions of h-BN in LB components,emphasizing the molecular-level mechanisms responsible for performance improvements.Finally,the review concludes by presenting the current challenges and prospects of integrating h-BN nanomaterials into battery research.展开更多
文摘The poor oxidation stability of ether-based solvents has long been a major challenge limiting their practical application.To enhance the oxidative stability of ether-based electrolytes,the physicochemical properties of various glycol dimethyl ethers are screened,and diglyme(G2)is selected as the sole solvent for the electrolyte.Lithium bis(fluorosulfonyl)imide(LiFSI),a highly dissociative salt,is used as the primary salt;while lithium nitrate(LiNO_(3))and lithium difluorophosphate(LiDFP),which have small ionic sizes and strong binding energies,are added as secondary salts.The resulting electrolyte can modulate the electric double layer structure by NO_(3)^(-) and DFP^(-) on the cathode side,leading to an increased Liþconcentration that is originally repelled by the cathode.Additionally,the oxidation stability of the electrolyte is improved and the formed electrode-electrolyte interphase is more uniform and stable,thereby enhancing the electrochemical performance of the cells.As a result,cells assembled with a total of 1 M ternary lithium salts in G2 solvent can operate at high voltage of 4.4 V.The LijjNCM811 cells maintain 80.2%capacity retention after 270 cycles at room temperature,with an average Coulombic efficiency of 99.5%,and exhibit 88.4%capacity retention after 200 cycles at -30℃.
基金support by the National Natural Science Foundation of China(Nos.U20A20123,51874357,22379166)Natural Science Foundation for Distinguished Young Scholars of Hunan Province(No.2022JJ10089)。
文摘The sluggish reaction kinetics of the oxygen evolution reaction(OER)and methanol oxidation reaction(MOR)remain obstacles to the commercial promotion of water splitting and direct methanol fuel cells.Considering the vital role of noble metals in electrocatalytic activity,this work focuses on the rational synthesis of Ni-noble metal composite nanocatalysts for overcoming the drawbacks of high cost and susceptible oxidized surfaces of noble metals.The inherent catalytic activity is improved by the altered electronic structure and effective active sites of the catalyst induced by the size effect of noble metal clusters.In particular,a series of Ni-noble metal nanocomposites are successfully synthesized by partially introducing noble metal into Ni with porous interfacial defects derived from Ni-Al layered double hydroxide(LDH).The Ni_(10)Pd_(1)nanocomposite exhibits high OER catalytic activity with an overpotential of 0.279 V at 10 m A/cm^(2),surpassing Ni_(10)Ag_(1)and Ni_(10)Au_(1)counterparts.Furthermore,the average diameter of Pd clusters gradually increases from 5.57 nm to 44.44 nm with the increased proportion of doped Pd,leading to the passivation of catalytic activity due to the exacerbated surface oxidation of Pd in the form of Pd^(2+).After optimization,Ni_(10)Pd_(1)delivers significantly enhanced OER and MOR electroactivities and long-term stability compared to that of Ni_(2)Pd_(1),Ni_(1)Pd_(1)and Ni_(1)Pd_(2),which is conducive to the effective utilization of Pd and alleviation of surface oxidation.
文摘During restorative dental procedures,complete control over the operative site is critical for patient comfort,safety,and the operator’s access and visibility.The success of a fixed prosthesis depends on accurate impression making of the prepared finish lines on the abutment teeth.To optimise long-term outcomes for the fixed restoration,gingival retraction techniques should be used to decrease the marginal discrepancy among the restoration and the prepared abutment.Accurate marginal positioning of the restoration along the prepared finish line of the abutment is essential for therapeutic,preventive,and aesthetic purposes.
基金supported by the Nano&Material Technology Development Program through the National Research Foundation of Korea(NRF)funded by the Ministry of Science and ICT(RS-2024-00446825)by the Technology Innovation Program(RS-2024-00418815)funded by the Ministry of Trade,Industry&Energy(MOTIE,Korea).
文摘Rechargeable magnesium batteries(RMBs)are a cutting-edge energy storage solution,with several advantages over the state-of-art lithiumion batteries(LIBs).The use of magnesium(Mg)metal as an anode material provides a much higher gravimetric capacity compared to graphite,which is currently used as the anode material in LIBs.Despite the significant advances in electrolyte,the development of cathode material is limited to materials that operate at low average discharge voltage(<1.0 V vs.Mg/Mg^(2+)),and developing high voltage cathodes remains challenging.Only a few materials have been shown to intercalate Mg^(2+)ions reversibly at high voltage.This review focuses on the structural aspects of cathode material that can operate at high voltage,including the Mg^(2+)intercalation mechanism in relation to its electrochemical properties.The materials are categorized into transition metal oxides and polyanions and subcategorized by the intrinsic Mg^(2+)diffusion path.This review also provides insights into the future development of each material,aiming to stimulate and guide researchers working in this field towards further advancements in high voltage cathodes.
基金supported by the Japan Society for the Promotion of Science(JSPS)KAKENHI Grant Number JP22F22368,JP20H00392,and JP23H05459.
文摘This review focuses on the significant impact of heteroatom doping in enhancing the electronic properties and electrochemical performance of carbon materials for supercapacitors(SCs).Incorporating heteroatoms such as nitrogen,sulfur,phosphorus,fluorine,and boron modifies the carbon structure,creates defects and increases active sites,which improves electronic conductivity,ion accessibility,and surface wettability and reduces ion diffusion barriers.Additionally,certain heteroatoms can participate in electrochemical reactions,further enhancing SC performance.Although research in this area is still emerging,a deeper understanding of the mechanisms behind single and multi-doping systems is essential for developing next-generation materials.Future strategies for improving heteroatom-doped carbon materials include increasing heteroatom content to enhance specific capacitance,selecting suitable heteroatoms to expand the potential window and improve energy density,utilizing advanced in situ characterization techniques,and exploring the use of these materials in cost-effective SCs.The potential of heteroatom-doped carbon materials for SCs is promising,with their ability to improve energy density,power density,and cycling stability,making them competitive with other energy storage technologies.These advancements will be key to broadening their practical applications,including electric vehicles,portable electronics,and grid energy storage,and will contribute to more efficient,long-lasting,and environmentally friendly energy storage solutions.
基金supported by the Natural Science Foundation of China(22408278,22275139,21971190,U21A2077)the Key Project of Natural Science Foundation of Tianjin City(Contract No.22JCZDJC00510)Key Laboratory of Functional Inorganic Material Chemistry(Heilongjiang University),Ministry of Education。
文摘Solar-driven hydrogen peroxide(H_(2)O_(2))production offers a sustainable and environmentally friendly alternative to the traditional anthraquinone oxidation method.Conjugated polymers(CPs)are emerging as promising photocatalysts for H_(2)O_(2)production due to their unique electronic,optical properties,and tunable structures.However,the high exciton binding energy of CPs hinders efficient exciton dissociation and charge separation,limiting their photocatalytic performance.In this work,we synthesized scandium(Sc)atoms decorated CPs with enhanced ordered stacking and crystallinity by introducing benzaldehyde as an end-capping reagent.The strong interaction between charged Sc atoms and electrons facilitates exciton dissociation and improves charge transfer capability.Furthermore,the Lewis acidic nature of Sc atoms promotes oxygen adsorption and enhances the stabilization of superoxide anion intermediate(·O_(2)^(-)).As a result,the as-synthesized photocatalysts exhibit a high H_(2)O_(2)production rate of 18μmol h^(-1)in pure water,which is three times that of pristine CPs,This work provides valuable insights into the design of organic polymer photocatalysts for various photocatalytic reactions.
基金financial support from the National Natural Science Foundation of China(No.22072183)the Natural Science Foundation of Hunan Province,China(No.2022JJ30690)supported in part by the High Performance Computing Center of Central South University。
文摘Three-dimensional(3D)covalent organic frameworks(COFs)have attracted extensive attention as photocatalysts for CO_(2)reduction reactions.Introducing metal atoms is essential for enhancing activity,but previous metal sites in 3D COFs predominantly exhibit symmetrical coordination,making them unsuitable for CO_(2)activation.Here,we design a 3D COF with 2,2'-pyridine linked around tetra-(4-anilyl)methane(TCM-Bpy-COF),where Co^(2+)is asymmetrically coordinated by bipyridine and acetates(TCMBpy-COF-CoAc).The TCM-Bpy-COF-CoAc exhibits outstanding photocatalytic CO_(2)reduction performance under weak visible light,achieving a CO evolution rate of 26,650μmol g^(-1)h^(-1)under 5 W of lightemitting-diode(LED)lamp and high apparent quantum efficiency.The performance far exceeds that of symmetrically coordinated bipyridine-Co-bipyridine TCM-Bpy-COF and surpasses most reported COF-based photocatalysts.In-situ spectral characterizations and theoretical calculations show that asymmetric N,O-coordination around the Co^(2+)center polarizes electron density and lowers reaction energy barriers of^(*)COOH intermediates,enhancing the conversion of CO_(2)to CO.This work inspires the design of 3D COF-based photocatalysts with highly catalytic efficiency.
基金the National Key R&D Program of China(No.2021YFA1500800)National Natural Science Foundation of China(No.22072106).
文摘Methane chemistry is one of the“Holy Grails of catalysis”.It is highly desirable but challenge to transform methane into value-added chemicals,because of its high C-H bonding energy(435 kJ/mol),lack ofπbonding or unpaired electrons.Currently,commercial methane conversion is usually carried out in harsh conditions with enormous energy input.Photocatalytic partial oxidation of methane to liquid oxygenates(PPOMO)is a future-oriented technology towards realizing high efficiency and high selectivity under mild conditions.The selection of oxidant is crucial to the PPOMO performance.Hence,attentions are paid to the research progress of PPOMO with various oxidants(O_(2),H_(2)O,H_(2)O_(2)and other oxidants).Moreover,the activation of the selected oxidants is also highly emphasized.Meanwhile,we summarized the methane activation mechanisms focusing on the C-H bond that was broken mainly by·OH radical,O-specie or photogenerated hole(h+).Finally,the challenges and prospects in this subject are briefly discussed.
基金supported by the Korea Meteorological Administration Research and Development Program “Developing Application Technology for Atmospheric Research Aircraft” (Grant No. KMA2018-00222)
文摘This study evaluated the simulation performance of mesoscale convective system(MCS)-induced precipitation,focusing on three selected cases that originated from the Yellow Sea and propagated toward the Korean Peninsula.The evaluation was conducted for the European Centre for Medium-Range Weather Forecasts(ECMWF)and National Centers for Environmental Prediction(NCEP)analysis data,as well as the simulation result using them as initial and lateral boundary conditions for the Weather Research and Forecasting model.Particularly,temperature and humidity profiles from 3D dropsonde observations from the National Center for Meteorological Science of the Korea Meteorological Administration served as validation data.Results showed that the ECMWF analysis consistently had smaller errors compared to the NCEP analysis,which exhibited a cold and dry bias in the lower levels below 850 hPa.The model,in terms of the precipitation simulations,particularly for high-intensity precipitation over the Yellow Sea,demonstrated higher accuracy when applying ECMWF analysis data as the initial condition.This advantage also positively influenced the simulation of rainfall events on the Korean Peninsula by reasonably inducing convective-favorable thermodynamic features(i.e.,warm and humid lower-level atmosphere)over the Yellow Sea.In conclusion,this study provides specific information about two global analysis datasets and their impacts on MCS-induced heavy rainfall simulation by employing dropsonde observation data.Furthermore,it suggests the need to enhance the initial field for MCS-induced heavy rainfall simulation and the applicability of assimilating dropsonde data for this purpose in the future.
基金support from the Tangshan Talent Funding Project(A202202007)the National Natural Science Foundation of China(21703065)+1 种基金the Natural Science Foundation of Hebei Province(B2018209267,E2022209039)the Basic Science Center Program for Ordered Energy Conversion of the National Natural Science Foundation of China(51888103).
文摘Molybdenum disulfide(MoS_(2))has garnered significant attention in the field of catalysis due to the high density of active sites in its unique two-dimensional(2D)structure,which could be developed into numerous high-performance catalysts.The synthesis of ultra-small MoS2 particles(<10 nm)is highly desired in various experimental studies.The ultra-small structure could often lead to a distinct S-Mo coordination state and nonstoichiometric composition in MoSx,minimizing in-plane active sites of the 2D structure and making it probable to regulate the atomic and electronic structure of its intrinsic active sites on a large extent,especially in MoSx clusters.This article summarizes the recent progress of catalysis over ultra-small undoped MoS_(2) particles for renewable fuel production.Through a systematic review of their synthesis,structural,and spectral characteristics,as well as the relationship between their catalytic performance and inherent defects,we aim to provide insights into catalysis over this matrix that may potentially enable advancement in the development of high-performance MoS_(2)-based catalysts for sustainable energy generation in the future.
基金supported by the Global Joint Research Program funded by the Pukyong National University(202411790001).
文摘Magnesium-ion batteries(MIBs)are promising candidates for lithium-ion batteries because of their abundance,non-toxicity,and favorable electrochemical properties.This review explores the reaction mechanisms and electrochemical characteristics of Mg-alloy anode materials.While Mg metal anodes provide high volumetric capacity and dendrite-free electrodeposition,their practical application is hindered by challenges such as sluggish Mg^(2+)ion diffusion and electrolyte compatibility.Alloy-type anodes that incorporate groups XIII,XIV,and XV elements have the potential to overcome these limitations.We review various Mg alloys,emphasizing their alloying/dealloying reaction mechanisms,their theoretical capacities,and the practical aspects of MIBs.Furthermore,we discuss the influence of the electrolyte composition on the reversibility and efficiency of these alloy anodes.Emphasis is placed on overcoming current limitations through innovative materials and structural engineering.This review concludes with perspectives on future research directions aimed at enhancing the performance and commercial viability of Mg alloy anodes and contributing to the development of high-capacity,safe,and cost-effective energy storage systems.
基金by JST FOREST Program(Grant No.JPMJFR203W,Japan)MEXT through Grant-in-Aid for Scientific Research(B)(No.19H02473,2019-2021)+2 种基金Grant-in-Aid for Scientific Research on Innovative Areas(Research in a proposed research area)(No.18H05456,2018-2022)the partial support through the research grant funded by the Amada Foundation(2022-2023)the financial support from the Amada Foundation(AF-2022017-B2).L.L.gratefully acknowledges the financial support provided by China Scholarship Council(No.201806295030)and thanks Dr.Elango Chandiran。
文摘Dynamic transformation(DT)of austenite(γ)to ferrite(α)in the hot deformation of various carbon steels was widely investigated.However,the nature of DT remains unclear due to the lack of quantitative analysis of stress partitioning between two phases and the uncertainty of local distribution of substitu-tional elements at the interface in multi-component carbon steels used in the previous studies.Therefore,in the present study,a binary Fe-Ni alloy withα+γduplex microstructure in equilibrium was prepared and isothermally compressed inα+γtwo-phase region to achieve a quantitative analysis of microstruc-ture evolution,stress partitioning,and thermodynamics during DT.γtoαDT during isothermal compres-sion andαtoγreverse transformation on isothermal annealing under unloaded condition after deforma-tion were accompanied by Ni partitioning.The lattice strains during thermomechanical processing were obtained via in-situ neutron diffraction measurement,based on which the stress partitioning behavior betweenγandαwas discussed by using the generalized Hooke’s law.A thermodynamic framework for the isothermal deformation in solids was established based on the basic laws of thermodynamics,and it was shown that the total Helmholtz free energy change in the deformable material during the isothermal process should be smaller than the work done to the deformable material.Under the present thermody-namic framework,the microstructure evolution in the isothermal compression of Fe-14Ni alloy was well explained by considering the changes in chemical free energy,plastic and elastic energies,and the work done to the material.In addition,the stabilization of the softαphase in Fe-14Ni alloy by deformation was rationalized since theγtoαtransformation decreased the total Helmholtz free energy by decreasing the elastic and dislocation energies.
文摘The exploration of newer antibacterial strategies is driven by antibiotic‐resistant microbes that cause serious public health issues.In recent years,nanoscale materials have developed as an alternative method to fight infections.Despite the fact that many nanomaterials have been discovered to be harmful,numerous researchers have shown a keen interest in nanoparticles(NPs)made of noble metals like silver,gold and platinum.To make environmentally safe NPs from plants,green chemistry and nanotechnology have been combined to address the issue of toxicity.The study of bimetallic nanoparticles(BNPs)has increased tremendously in the past 10 years.The production of BNPs mediated by natural extracts is straightforward,low cost and environmentally friendly.Due to their low toxicity,safety and biological stability,noble BNPs with silver,gold,platinum and palladium have the potential to be used in biomedical applications.They have a significant impact on human health and are used in medicine and pharmacy due to their biological characteristics,which include catalytic,antioxidant,antibacterial,antidiabetic,anticancer,hepatoprotective and regenerative activity.
基金supported by the Center for Functional Materials,National Institute for Materials Science,Japan,Egyptian Petroleum Research Institute,Egypt,and Nano-Environmental Uint,Theodor Bilharz Research Institute,Egypt。
文摘The design of nanostructured materials occupies a privileged position in the development and management of affordable and effective technology in the antibacterial sector.Here,we discuss the antimicrobial properties of three carbonaceous nanoblades and nanodarts materials of graphene oxide(GO),reduced graphene oxide(RGO),and single-wall carbon nanotubes(SWCNTs)that have a mechano-bactericidal effect,and the ability to piercing or slicing bacterial membranes.To demonstrate the significance of size,morphology and composition on the antibacterial activity mechanism,the designed nanomaterials have been characterized.The minimum inhibitory concentration(MIC),standard agar well diffusion,and transmission electron microscopy were utilized to evaluate the antibacterial activity of GO,RGO,and SWCNTs.Based on the evidence obtained,the three carbonaceous materials exhibit activity against all microbial strains tested by completely encapsulating bacterial cells and causing morphological disruption by degrading the microbial cell membrane in the order of RGO>GO>SWCNTs.Because of the external cell wall structure and outer membrane proteins,the synthesized carbonaceous nanomaterials exhibited higher antibacterial activity against Gram-positive bacterial strains than Gram-negative and fungal microorganisms.RGO had the lowest MIC values(0.062,0.125,and 0.25 mg/mL against B.subtilis,S.aureus,and E.coli,respectively),as well as minimum fungal concentrations(0.5 mg/mL for both A.fumigatus and C.albicans).At 12 hr,the cell viability values against tested microbial strains were completely suppressed.Cell lysis and death occurred as a result of severe membrane damage caused by microorganisms perched on RGO nanoblades.Our work gives an insight into the design of effective graphene-based antimicrobial materials for water treatment and remediation.
基金financially supported by the National Natural Science Foundation of China(51702291)the China Postdoctoral Science Foundation(2020M682352)+2 种基金the State Key Laboratory of Powder Metallurgy,Central South University,Changsha,Chinasupport from the Project of Zhongyuan Critical Metals Laboratory(GJJSGFYQ202336)the Youth Talent Program of Zhengzhou University(32340398)
文摘Growing energy demand drives the rapid development of clean and reliable energy sources.In the past years,the exploration of novel materials with considerable efficiency and durability has drawn attention in the area of electrochemical energy conversion.Transition metal macrocyclic metallophthalocyanines(MPcs)-based catalysts with a peculiar 2D constitution have emerged with a promising future account of their highly structural tailorability and molecular functionality which greatly extend their functionalities as electrocatalytic materials for energy conversion.This review summarizes the systematic engineering of synthesis of MPcs and their analogs in detail,and mostly pays attention to the frontier research of MPc-based high-performance catalysts toward different electrocatalytic processes concerning hydrogen,oxygen,water,carbon dioxide,and nitrogen,with a particular focus on discussing the interrelationship between the electrocatalytic activity and component/structure,as well as functional applications of MPcs.Finally,we give the gaps that need to be addressed after much thought.
基金the Japan Society for the Promotion of Science(JSPS)KAKENHI Grant Number JP18F18714Cryogenic Station,Research Network and Facility Services Division,National Institute for Materials Science(NIMS),Japansupported by the ARC Linkage Project(LP200200689)。
文摘The development of superconducting joining technology for reacted magnesium diboride(MgB_(2))conductors remains a critical challenge for the advancement of cryogen-free MgB_(2)-based magnets for magnetic resonance imaging(MRI).Herein,the fabrication of superconducting joints using reacted carbon-doped multifilament MgB_(2)wires for MRI magnets is reported.To achieve successful superconducting joints,the powder-in-mold method was employed,which involved tuning the filament protection mechanism,the powder compaction pressure,and the heat treatment condition.The fabricated joints demonstrated clear superconducting-to-normal transitions in self-field,with effective magnetic field screening up to 0.5 T at 20 K.To evaluate the interface between one of the MgB_(2)filaments and the MgB_(2)bulk within the joint,serial sectioning was conducted for the first time in this type of superconducting joint.The serial sectioning revealed space formation at the interface,potentially caused by the volume shrinkage associated with the MgB_(2)formation or the combined effect of the volume shrinkage and the different thermal expansion coefficients of the MgB_(2)bulk,the filament,the mold,and the sealing material.These findings are expected to be pivotal in developing MgB_(2)superconducting joining technology for MRI magnet applications through interface engineering.
基金supported by National Natural Science Foundation of China(No.92261109)Natural Science Foundation of Fujian Province(No.2020J05080)+3 种基金Project Funded by China Postdoctoral Science Foundation(No.2023M733496)Natural Science Foundation of Xiamen(No.3502Z20206080)Fujian Science&Technology Innovation Laboratory for Optoelectronic Information of China(No.2021ZR110)Recruitment Program of Global Youth Experts,Youth Innovation Promotion Association CAS(No.2021302).
文摘Electron-deficient viologens are widely used as ligands or structure-directing agents(SDAs)to synthesize crystalline X-ray induced photochromic materials.Here,a new rational strategy of anion-directed fold-ing a flexible cation(H_(2)imb)^(2+)((H_(2)imb)^(2+)=di-protonated 2,3-bis(imidazolin-2-yl)-2,3-dimethylbutane)has been developed.Electron-donating Cl−and(ZnCl4)2−are used to direct folding a flexible electron-deficient(H_(2)imb)^(2+)cation.Three complexes(H_(2)imb)(NO_(3))2(1),(H_(2)imb)Cl2·H_(2)O(2),and(H_(2)imb)ZnCl4(3)have been synthesized in which(H_(2)imb)^(2+)crystallize in an anti-conformation,88.8°-gauche,and 51.8°-gauche,respectively.In contrary to X-ray silent complex 1,X-ray induced photochromism has been achieved in both complex 2 and 3.An intermolecular charge-transfer mechanism has been elucidated and the anion directed folding of(H_(2)imb)^(2+)has been validated to be critical to yield colored long-lived charge-separated states.
文摘A dye-sensitized photocatalyst combining Pt-loaded TiO_(2) and Ru(Ⅱ)tris-diimine sensitizer(RuP)was constructed and its activity for photochemical hydrogen evolution was compared with that of Pt-intercalated HCa_(2)Nb_(3)O_(10) nanosheets.When the sacrificial donor ethylenediaminetetraacetic acid(EDTA)disodium salt dihydrate was used,RuP/Pt/TiO_(2) showed higher activity than RuP/Pt/HCa_(2)Nb_(3)O_(10).In contrast,when NaI(a reversible electron donor)was used,RuP/Pt/TiO_(2) showed little activity due to back electron transfer to the electron acceptor(I_(3)-),which was gener-ated as the oxidation product of I-.By modification with anionic polymers(sodium poly(styrenesulfonate)or sodium polymethacrylate)that could inhibit the scavenging of conduction band electrons by I_(3)-,the H_(2) production activity from aqueous NaI was improved,but it did not exceed that of RuP/Pt/HCa_(2)Nb_(3)O_(10).Transient absorption measurements showed that the rate of semiconductor-to-dye back electron transfer was slower in the case of TiO_(2) than HCa_(2)Nb_(3)O_(10),but the electron transfer reaction to I3-was much faster.These results indicate that Pt/TiO_(2) is useful for reactions with sacrificial reductants(e.g.,EDTA),where the back electron transfer reaction to the more reducible product can be neglected.However,more careful design of the catalyst will be nec-essary when a reversible electron donor is employed.
基金AP is grateful for the financial support of Science Foundation Ireland(SFI)under grant number 18/SIRG/5621 and Enterprise Ireland under grant number CS20212089DG is grateful to the Australian Research Council(ARC)for a support in the frame of an ARC Laureate project No FL160100089.Open access funding provided by IReL.
文摘The current global warming,coupled with the growing demand for energy in our daily lives,necessitates the development of more efficient and reliable energy storage devices.Lithium batteries(LBs)are at the forefront of emerging power sources addressing these challenges.Recent studies have shown that integrating hexagonal boron nitride(h-BN)nanomaterials into LBs enhances the safety,longevity,and electrochemical performance of all LB components,including electrodes,electrolytes,and separators,thereby suggesting their potential value in advancing eco-friendly energy solutions.This review provides an overview of the most recent applications of h-BN nanomaterials in LBs.It begins with an informative introduction to h-BN nanomaterials and their relevant properties in the context of LB applications.Subsequently,it addresses the challenges posed by h-BN and discusses existing strategies to overcome these limitations,offering valuable insights into the potential of BN nanomaterials.The review then proceeds to outline the functions of h-BN in LB components,emphasizing the molecular-level mechanisms responsible for performance improvements.Finally,the review concludes by presenting the current challenges and prospects of integrating h-BN nanomaterials into battery research.
