With the rapid development of twodimensional MXene materials,numerous preparation strategies have been proposed to enhance synthesis efficiency,mitigate environmental impact,and enable scalability for large-scale prod...With the rapid development of twodimensional MXene materials,numerous preparation strategies have been proposed to enhance synthesis efficiency,mitigate environmental impact,and enable scalability for large-scale production.The compound etching approach,which relies on cationic oxidation of the A element of MAX phase precursors while anions typically adsorb onto MXene surfaces as functional groups,remains the main prevalent strategy.By contrast,synthesis methodologies utilizing elemental etching agents have been rarely reported.Here,we report a new elemental tellurium(Te)-based etching strategy for the preparation of MXene materials with tunable surface chemistry.By selectively removing the A-site element in MAX phases using Te,our approach avoids the use of toxic fluoride reagents and achieves tellurium-terminated surface groups that significantly enhance sodium storage performance.Experimental results show that Te-etched MXene delivers substantially higher capacities(exceeding 50%improvement over conventionally etched MXene)with superior rate capability,retaining high capacity at large current densities and demonstrating over 90%capacity retention after 1000 cycles.This innovative synthetic strategy provides new insight into controllable MXene preparation and performance optimization,while the as-obtained materials hold promises for high-performance sodium-ion batteries and other energy storage systems.展开更多
Thermal analysis technique has been used for a long time,in both ferrous and nonferrous industries for evaluating the metallurgical quality of the liquid metal before casting.However,obtaining a proper microstructure ...Thermal analysis technique has been used for a long time,in both ferrous and nonferrous industries for evaluating the metallurgical quality of the liquid metal before casting.However,obtaining a proper microstructure in a standard cup does not ensure that the microstructure is correct in real parts which may solidify at very different cooling rates.For this study,alloy A356 with different metal quality in terms of modification and grain refinement was tested.Different cooling rates were obtained by using cylindrical test samples with various diameters cast in sand and metallic moulds.The correlation between microstructure features such as grain size,modification rate and secondary dendrite arm spacing (SDAS) measured in the standard thermal analysis cup with those obtained in the cylindrical test parts has been investigated.Thus,knowing the thermal modulus and the mould type it is possible to establish the required grain size and modification rate in the standard cup in order to get a desired structure in a real part.Corrective actions can then be taken in order to improve the metallurgical quality before casting the part.展开更多
As one of the promising energy storage and conversion systems,supercapacitors(SCs)are highly favored owing to their high power density and good service life.Among all the key components of supercapacitor devices,the d...As one of the promising energy storage and conversion systems,supercapacitors(SCs)are highly favored owing to their high power density and good service life.Among all the key components of supercapacitor devices,the design and investigation of electrode materials play an essential role in determining the whole electrochemical charge storage performance.Recently,nanocarbon-based materials(e.g.,graphene,carbon dots,graphene quantum dots,etc.)have been widely used as SC electrode materials because of their good physical structure and chemical properties,providing a new route to further improve the energy density and life span of SCs.Here,we review the latest progress of nanocarbon-based materials(including nanocarbon and nanocarbon-based composite materials)as electrode materials in SCs application.The recent progress of carbon dots,graphene,carbon nanotubes,and other nanocarbon materials electrodes is summarized,while the capacitance and energy density of the above nanocarbon electrodes still need to be improved.Then,the preparation and performance of nanocarbonbased composite electrodes comprising transition metal oxides,conductive polymer,and metal-organic framework derived porous carbon are reviewed.Finally,we outline major challenges and propose some ideas on building better nanocarbon-based SC electrodes.展开更多
A melt maintained for hours in a press pour unit allowed the following changes over time from spheroidal graphite to compacted graphite iron by casting thermal cups at regular time intervals.This provided extensive ex...A melt maintained for hours in a press pour unit allowed the following changes over time from spheroidal graphite to compacted graphite iron by casting thermal cups at regular time intervals.This provided extensive experimental information for checking the possibility of simulating solidification of compacted graphite irons by means of a microstructure modelling approach.During solidification,compacted graphite develops very much as lamellar graphite but with much less branching.On this basis,a simulation of the thermal analysis records was developed which considers solidification proceeding in a pseudo binary Fe-C system.The simulated curves were compared with the experimental ones obtained from three representative alloys that cover the whole microstructure change during the holding of the melt.The most relevant result is that the parameter describing branching capability of graphite is the most important for reproducing the minimum eutectic temperature and the recalescence which are so characteristic of the solidification of compacted graphite cast irons.展开更多
The corrosion resistance of three Mg alloys containing rare-earth elements(WE43,EV31 and ZE41)was studied and compared to that of two Mg-Al alloys(AZ31 and AZ91)and of pure Mg(99.95 wt.%).Current-voltage curves and el...The corrosion resistance of three Mg alloys containing rare-earth elements(WE43,EV31 and ZE41)was studied and compared to that of two Mg-Al alloys(AZ31 and AZ91)and of pure Mg(99.95 wt.%).Current-voltage curves and electrochemical impedance measurements were performed with rotating disk electrodes in an aerated 0.1 M Na_(2)SO_(4)solution.For all the alloys,it was confirmed that the intermetallic particles acted as local cathodes and that more protective films were formed on the alloys surface by comparison with the pure Mg.Corrosion rates were determined from inductive coupled plasma-optical emission spectroscopy measurements and from the electrochemical measurements.Higher corrosion rates were observed for the rare-earth Mg alloys compared to the AZ series alloys.These data allowed the corrosion mechanisms to be discussed.展开更多
The characterization of the shells of snails Achatina achatina and Lanistes varicus indicates that they contain calcium carbonate (98%) essentially aragonite, and organic matter (2%). The heating at 500°C during ...The characterization of the shells of snails Achatina achatina and Lanistes varicus indicates that they contain calcium carbonate (98%) essentially aragonite, and organic matter (2%). The heating at 500°C during three hours (3 h) has destroyed their constitutive organic matter, converted the aragonite form completely into the calcite and reduced their specific surfaces. The effects of these modifications have been revealed in the adsorption in aqueous environment of methylene blue (MB) and methyl orange (MO) which are respectively cationic and anionic dyes. The results showed that the sorption of these dyes on the raw shells is more important than the heated shells. The methylene blue has more affinity for shells than methyl orange. Between these two types of snails, the shells of Lanistes varicus have a higher capacity of adsorption. This sorption of the methylene blue is more in relationship with the Freundlich model ( for EG and for EA) comparatively to Langmuir model If the shells of these snails were calcined before using for the cicatrizing of the human cutaneous wounds in Benin. In the case of the sorption of organic molecule, it will be necessary to avoid submitting them to a preliminary heat treatment.展开更多
Differential thermal analysis experiments have been performed on samples machined from Y2-blocks cast with different high-silicon spheroidal graphite irons. Depending on magnesium, silicon, cerium and antimony content...Differential thermal analysis experiments have been performed on samples machined from Y2-blocks cast with different high-silicon spheroidal graphite irons. Depending on magnesium, silicon, cerium and antimony content, the as-cast microstructure showed various levels of chunky graphite in the central part of the blocks. In contrast, the microstructure of the materials after remelting and resolidification during differential thermal analysis consisted of lamellar or compacted graphite. The formation of chunky graphite in the as-cast microstructure is rationalized using an index or silicon equivalent that has been recently suggested. The differences in the microstructures after differential thermal analysis are discussed in terms of available free magnesium. Emphasis is finally put on the striking differences in characteristic size of the microstructures made of compacted graphite as compared to lamellar graphite and chunky graphite. This leads to tentative conclusions about growth of compacted and chunky graphite which would be worthy of further experimental investigations.展开更多
We report a simple method for preparing copper（II） molybdate（CuMoO_4） powders via a combustion-like process. A gel was first prepared by the polymerizable complex method, where citric acid was used as a complexing...We report a simple method for preparing copper（II） molybdate（CuMoO_4） powders via a combustion-like process. A gel was first prepared by the polymerizable complex method, where citric acid was used as a complexing and polymerizing agent and nitric acid was used as an oxidizing agent. The thermal decomposition behavior of the（CuMo）-precursor gel was studied by thermogravimetry–differential thermal analysis（TG–DTA）, Fourier transform infrared spectroscopy（FTIR）, and X-ray diffraction（XRD）. We observed that the crystallization of CuMoO_4 powder was completed at 450°C. The obtained homogeneous powder was composed of grains with sizes in the range from 150 to 500 nm and exhibited a specific surface area of approximately 5 m^2/g. The average grain size increased with increasing annealing temperature. The as-prepared CuMoO_4 crystals showed a strong green photoluminescence emission at room temperature under excitation at 290 nm, which we mainly interpreted on the basis of the Jahn-Teller effect on [MoO_4^（2-）] complex anions. We also observed that the photoluminescence intensity increased with increasing crystallite size.展开更多
MoS_(2) is a promising anode material in sodium-ion battery technologies for possessing high theoretical capacity.However,the sluggish Na^(+) diffusion kinetics and low electronic conductivity hinder the promises.Here...MoS_(2) is a promising anode material in sodium-ion battery technologies for possessing high theoretical capacity.However,the sluggish Na^(+) diffusion kinetics and low electronic conductivity hinder the promises.Herein,a unique MoS_(2)/FeS_(2)/C heterojunction with abundant defects and hollow structure(MFCHHS)was constructed.The synergy of defect engineering in MoS_(2),FeS_(2),and the carbon layer of MFCHHS with a larger specific surface area provides multiple storage sites of Na^(+)corresponding to the surface-controlled process.The MoS_(2)/FeS_(2)/C heterostructure and rich defects in MoS_(2) and carbon layer lower the Na^(+) diffusion energy barrier.Additionally,the construction of MoS_(2)/FeS_(2) heterojunction promotes electron transfer at the interface,accompanying with excellent conductivity of the carbon layer to facilitate reversible electrochemical reactions.The abundant defects and mismatches at the interface of MoS_(2)/FeS_(2) and MoS_(2)/C heterojunctions could relieve lattice stress and volume change sequentially.As a result,the MFCHHS anode exhibits the high capacity of 613.1 mA h g^(-1)at 0.5 A g^(-1) and 306.1 mA h g^(-1) at 20 A g^(-1).The capacity retention of 85.0%after 1400 cycles at 5.0 A g^(-1) is achieved.The density functional theory(DFT)calculation and in situ transmission electron microscope(TEM),Raman,ex-situ X-ray photon spectroscopy(XPS)studies confirm the low volume change during intercalation/deintercalation process and the efficient Na^(+)storage in the layered structure of MoS_(2) and carbon layer,as well as the defects and heterostructures in MFCHHS.We believe this work could provide an inspiration for constructing heterojunction with abundant defects to foster fast electron and Na^(+) diffusion kinetics,resulting in excellent rate capability and cycling stability.展开更多
MAX phases are gaining attention as precursors of two-dimensional MXenes that are intensively pursued in applications for electrochemical energy storage.Here,we report the preparation of V_(2)SnC MAX phase by the molt...MAX phases are gaining attention as precursors of two-dimensional MXenes that are intensively pursued in applications for electrochemical energy storage.Here,we report the preparation of V_(2)SnC MAX phase by the molten salt method.V_(2)SnC is investigated as a lithium storage anode,showing a high gravimetric capacity of 490 mAh g−1 and volumetric capacity of 570 mAh cm^(−3) as well as superior rate performance of 95 mAh g^(−1)(110 mAh cm^(−3))at 50 C,surpassing the ever-reported performance of MAX phase anodes.Sup-ported by operando X-ray diffraction and density functional theory,a charge storage mechanism with dual redox reaction is proposed with a Sn-Li(de)alloying reaction that occurs at the edge sites of V_(2)SnC particles where Sn atoms are exposed to the electrolyte followed by a redox reaction that occurs at V_(2)C layers with Li.This study offers promise of using MAX phases with M-site and A-site elements that are redox active as high-rate lithium storage materials.展开更多
The study of pickling of the EL21T6 substrate in a nitric acid bath firstly provided knowledge of the influence of the different experimental parameters(concentration of acid,temperature and stirring of the solution)i...The study of pickling of the EL21T6 substrate in a nitric acid bath firstly provided knowledge of the influence of the different experimental parameters(concentration of acid,temperature and stirring of the solution)in relation to the etching rate.This experimental part led to the choice of standard pickling(T_(bath)=25℃,moderate stirring(250 rpm),[HNO_(3)]=1.20 mol/L,duration of 2 min)so as to obtain constant removal of material,even after several uses of the pickling bath.SEM observations also confirmed that in these operating conditions,pickling concerns both the grains of the matrix and the precipitates of type Mg3(Nd,Gd),leading to uniform removal of material from the surface.Working from a number of assumptions,thermodynamic and chemical kinetic studies then allowed a pickling mechanism to be proposed and led to obtaining values for the corresponding kinetic parameters(order of reaction,constant of mean rate,activation energy)to be obtained.展开更多
Energy storage and conversion have attained significant intere st owing to its important applications that reduce CO2 emission through employing green energy.Some promising technologies are included metalair batteries...Energy storage and conversion have attained significant intere st owing to its important applications that reduce CO2 emission through employing green energy.Some promising technologies are included metalair batteries,metal-sulfur batteries,metal-ion batteries,electrochemical capacitors,etc.Here,metal elements are involved with lithium,sodium,and magnesium.For these devices,electrode materials are of importance to obtain high performance.Two-dimensional(2 D) materials are a large kind of layered structured materials with promising future as energy storage materials,which include graphene,black phosporu s,MXenes,covalent organic frameworks(COFs),2 D oxides,2 D chalcogenides,and others.Great progress has been achieved to go ahead for 2 D materials in energy storage and conversion.More researchers will join in this research field.Under the background,it has motivated us to contribute with a roadmap on ’two-dimensional materials for energy storage and conversion.展开更多
Computational modeling methods,including molecular dynamics(MD)and Monte Carlo(MC)simulations,and density functional theory(DFT),are receiving booming interests for exploring charge storage mechanisms of electrochemic...Computational modeling methods,including molecular dynamics(MD)and Monte Carlo(MC)simulations,and density functional theory(DFT),are receiving booming interests for exploring charge storage mechanisms of electrochemical energy storage devices.These methods can effectively be used to obtain molecular scale local information or provide clear explanations for novel experimental findings that cannot be directly interpreted through experimental investigations.This short review is dedicated to emphasizing recent advances in computational simulation methods for exploring the charge storage mechanisms in typical nanoscale materials,such as nanoporous carbon materials,2 D MXene materials,and metal-organic framework electrodes.Beyond a better understanding of charge storage mechanisms and experimental observations,fast and accurate enough models would be helpful to provide theoretical guidance and experimental basis for the design of new high-performance electrochemical energy storage devices.展开更多
This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction b...This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction between accessories carbonates present in raw fibrous palygorskite clay and titanyl sulfate (TiOSO<sub>4</sub>) precursor under variable grinding conditions, essentially ball/solid matter mass ratio and rotation velocity. This yielded after air annealing at 600%C for 1 h to the immobilization of anatase TiO<sub>2</sub> nanoparticles (≈8 nm of average size) as evidenced by XRD and TEM analyses. Once the conditions of elaboration were optimized, the photocatalytic properties were evaluated under 3 conditions: artificial UV radiation, artificial solar radiation (UV + visible range) and under dynamic solar illumination taking into account the discontinuities of the solar resource. The results allowed the estimation and comparison of the catalyst’s capabilities and showed its ability to work under natural irradiation. The so developed supported photocatalysts TiO<sub>2</sub>/Palygorskite exhibited a good activity towards the removal of Orange G (OG) dye from aqueous media under artificial UV and natural solar radiations.展开更多
Fe（3–x）O4 raspberry shaped nanostructures/graphene nanocomposites were synthesized by a one-step polyol-solvothermal method to be tested as electrode materials for Li-ion battery（LIB）. Indeed, Fe（3–x）O4 raspbe...Fe（3–x）O4 raspberry shaped nanostructures/graphene nanocomposites were synthesized by a one-step polyol-solvothermal method to be tested as electrode materials for Li-ion battery（LIB）. Indeed, Fe（3–x）O4 raspberry shaped nanostructures consist of original oriented aggregates of Fe（3–x）O4 magnetite nanocrystals, ensuring a low oxidation state of magnetite and a hollow and porous structure, which has been easily combined with graphene sheets. The resulting nanocomposite powder displays a very homogeneous spatial distribution of Fe（3–x）O4 nanostructures at the surface of the graphene sheets. These original nanostructures and their strong interaction with the graphene sheets resulted in very small capacity fading upon Li＋ion intercalation. Reversible capacity, as high as 660 m Ah/g, makes this material promising for anode in Li-ion batteries application.展开更多
Structural analogues of bicyclic peroxides belonging to the G factors family have been synthesised under Mannieh type conditions, followed by an autoxidation step furnishing exclusively the peroxide. As electron trans...Structural analogues of bicyclic peroxides belonging to the G factors family have been synthesised under Mannieh type conditions, followed by an autoxidation step furnishing exclusively the peroxide. As electron transfer from heine or free iron to peroxide is the first step in the mode of action ofartemisinin -like compound, Fe（fl） induced reduction was studied and the reactivity of the intermediate C-centered radical formed was correlated to the antimalarial activity. Dissociative electron transfer was studied by electrochemistry and allowed the evaluation of the standard reduction potentials and other pertinent thermochemical information. These bicyclic peroxides were evaluated in vitro against Plasmodium falciparum and revealed moderate to good activity.展开更多
MXenes are two-dimensional transition metal carbides and/or nitrides with unique physiochemical properties and have attracted extensive interest in numerous fields.However,current MXene synthesis methods are limited b...MXenes are two-dimensional transition metal carbides and/or nitrides with unique physiochemical properties and have attracted extensive interest in numerous fields.However,current MXene synthesis methods are limited by hazardous synthesis conditions,high production costs,or difficulty in largescale production.Therefore,a general,safe,cost-effective,and scalable synthesis method for MXenes is crucial.Here,we report the fast synthesis of MXenes in the open air using a molten salt-shielded synthesis(MS^(3))method,which uses Lewis-acid salts as etchants and a low-melting-point eutectic salt mixture as the reaction medium and shield to prevent MXene oxidation at high temperatures.Carbide and nitride MXenes,including Ti_(3)C_(2)T_(x),Ti_(2)CT_(x),Ti_(3)CNT_(x),and Ti_(4)N_(3)T_(x),were successfully synthesized using the MS^(3)method.We also present the flexibility of the MS^(3)method by scaling the etching process to large batches of 20 and 60 g of Ti_(3)AlC_(2)MAX precursor in one pot.When used as negative electrodes,the prepared MS^(3)-MXenes delivered excellent electrochemical properties for high-rate Li-ion storage.展开更多
High volumetric energy density energy storage devices are needed for many applications ranging from miniaturized electronics to electric vehicles[1,2].Two-dimensional(2D)nanosheets,such as graphene,MoS2,and MXene are ...High volumetric energy density energy storage devices are needed for many applications ranging from miniaturized electronics to electric vehicles[1,2].Two-dimensional(2D)nanosheets,such as graphene,MoS2,and MXene are great candidates for assembling compact sheets[1–5],as their horizontal stacking can achieve interlayer distances close to the diameter of electrolyte ions[1,6].The electrolyte ions confined between interlayers of those materials significantly improve the pore and porous volume utilization,thus achieving compact energy storage realized by ion desolvation[1].展开更多
Recently,multivalent aqueous calcium-ion batteries(CIBs)have attracted considerable attention as a possible alternative to Li-ion batteries.However,traditional Ca-ion storage materials show either limited rate capabil...Recently,multivalent aqueous calcium-ion batteries(CIBs)have attracted considerable attention as a possible alternative to Li-ion batteries.However,traditional Ca-ion storage materials show either limited rate capabilities and poor cycle life or insufficient specific capacity.Here,we tackle these limitations by exploring materials having a large interlayer distance to achieve decent specific capacities and one-dimensional architecture with adequate Ca-ion passages that enable rapid reversible(de)intercalation processes.In this work,we report the high-yield,rapid,and low-cost synthesis of 1D metal oxides MV_(3)O_(8)(M=Li,K),CaV_(2)O_(6),and CaV_(6)O_(16)·7H_(2)O(CVO)via a molten salt method.Firstly,using 1D CVO as electrode materials,we show high capacity 205 mA h g^(-1),long cycle life(>97%capacity retention after 200 cycles at 3.0 C),and high-rate performance(117 mA h g^(-1) at 12 C)for Ca-ion(de)intercalation.This work represents a step forward for the development of the molten salt method to synthesize nanomaterials and to help pave the way for the future growth of Ca-ion batteries.展开更多
基金supported by the National Natural Science Foundation of China(52472228,22309202)Natural Science Foundation of Sichuan Province(2023NSFSC1942)the Gusu Leading Talents Program(ZXL2023190)。
文摘With the rapid development of twodimensional MXene materials,numerous preparation strategies have been proposed to enhance synthesis efficiency,mitigate environmental impact,and enable scalability for large-scale production.The compound etching approach,which relies on cationic oxidation of the A element of MAX phase precursors while anions typically adsorb onto MXene surfaces as functional groups,remains the main prevalent strategy.By contrast,synthesis methodologies utilizing elemental etching agents have been rarely reported.Here,we report a new elemental tellurium(Te)-based etching strategy for the preparation of MXene materials with tunable surface chemistry.By selectively removing the A-site element in MAX phases using Te,our approach avoids the use of toxic fluoride reagents and achieves tellurium-terminated surface groups that significantly enhance sodium storage performance.Experimental results show that Te-etched MXene delivers substantially higher capacities(exceeding 50%improvement over conventionally etched MXene)with superior rate capability,retaining high capacity at large current densities and demonstrating over 90%capacity retention after 1000 cycles.This innovative synthetic strategy provides new insight into controllable MXene preparation and performance optimization,while the as-obtained materials hold promises for high-performance sodium-ion batteries and other energy storage systems.
基金supported by the Basque Government (Project:Manufacturing 0.0 Etortek 2008)Spanish Government (Singular Strategic Project,PSE integrAuto)
文摘Thermal analysis technique has been used for a long time,in both ferrous and nonferrous industries for evaluating the metallurgical quality of the liquid metal before casting.However,obtaining a proper microstructure in a standard cup does not ensure that the microstructure is correct in real parts which may solidify at very different cooling rates.For this study,alloy A356 with different metal quality in terms of modification and grain refinement was tested.Different cooling rates were obtained by using cylindrical test samples with various diameters cast in sand and metallic moulds.The correlation between microstructure features such as grain size,modification rate and secondary dendrite arm spacing (SDAS) measured in the standard thermal analysis cup with those obtained in the cylindrical test parts has been investigated.Thus,knowing the thermal modulus and the mould type it is possible to establish the required grain size and modification rate in the standard cup in order to get a desired structure in a real part.Corrective actions can then be taken in order to improve the metallurgical quality before casting the part.
基金financially supported by the National Natural Science Foundation of China (Nos.52172033 and 22005280)Anhui Province Key Research and Development Plan Project International Science and Technology Cooperation Special Project (No.202004b11020015)
文摘As one of the promising energy storage and conversion systems,supercapacitors(SCs)are highly favored owing to their high power density and good service life.Among all the key components of supercapacitor devices,the design and investigation of electrode materials play an essential role in determining the whole electrochemical charge storage performance.Recently,nanocarbon-based materials(e.g.,graphene,carbon dots,graphene quantum dots,etc.)have been widely used as SC electrode materials because of their good physical structure and chemical properties,providing a new route to further improve the energy density and life span of SCs.Here,we review the latest progress of nanocarbon-based materials(including nanocarbon and nanocarbon-based composite materials)as electrode materials in SCs application.The recent progress of carbon dots,graphene,carbon nanotubes,and other nanocarbon materials electrodes is summarized,while the capacitance and energy density of the above nanocarbon electrodes still need to be improved.Then,the preparation and performance of nanocarbonbased composite electrodes comprising transition metal oxides,conductive polymer,and metal-organic framework derived porous carbon are reviewed.Finally,we outline major challenges and propose some ideas on building better nanocarbon-based SC electrodes.
文摘A melt maintained for hours in a press pour unit allowed the following changes over time from spheroidal graphite to compacted graphite iron by casting thermal cups at regular time intervals.This provided extensive experimental information for checking the possibility of simulating solidification of compacted graphite irons by means of a microstructure modelling approach.During solidification,compacted graphite develops very much as lamellar graphite but with much less branching.On this basis,a simulation of the thermal analysis records was developed which considers solidification proceeding in a pseudo binary Fe-C system.The simulated curves were compared with the experimental ones obtained from three representative alloys that cover the whole microstructure change during the holding of the melt.The most relevant result is that the parameter describing branching capability of graphite is the most important for reproducing the minimum eutectic temperature and the recalescence which are so characteristic of the solidification of compacted graphite cast irons.
基金The authors gratefully acknowledge the IRT Saint-Exupery Surfinnov project partners,especially Mapaero and Prodem companies,for the financial support.
文摘The corrosion resistance of three Mg alloys containing rare-earth elements(WE43,EV31 and ZE41)was studied and compared to that of two Mg-Al alloys(AZ31 and AZ91)and of pure Mg(99.95 wt.%).Current-voltage curves and electrochemical impedance measurements were performed with rotating disk electrodes in an aerated 0.1 M Na_(2)SO_(4)solution.For all the alloys,it was confirmed that the intermetallic particles acted as local cathodes and that more protective films were formed on the alloys surface by comparison with the pure Mg.Corrosion rates were determined from inductive coupled plasma-optical emission spectroscopy measurements and from the electrochemical measurements.Higher corrosion rates were observed for the rare-earth Mg alloys compared to the AZ series alloys.These data allowed the corrosion mechanisms to be discussed.
文摘The characterization of the shells of snails Achatina achatina and Lanistes varicus indicates that they contain calcium carbonate (98%) essentially aragonite, and organic matter (2%). The heating at 500°C during three hours (3 h) has destroyed their constitutive organic matter, converted the aragonite form completely into the calcite and reduced their specific surfaces. The effects of these modifications have been revealed in the adsorption in aqueous environment of methylene blue (MB) and methyl orange (MO) which are respectively cationic and anionic dyes. The results showed that the sorption of these dyes on the raw shells is more important than the heated shells. The methylene blue has more affinity for shells than methyl orange. Between these two types of snails, the shells of Lanistes varicus have a higher capacity of adsorption. This sorption of the methylene blue is more in relationship with the Freundlich model ( for EG and for EA) comparatively to Langmuir model If the shells of these snails were calcined before using for the cicatrizing of the human cutaneous wounds in Benin. In the case of the sorption of organic molecule, it will be necessary to avoid submitting them to a preliminary heat treatment.
文摘Differential thermal analysis experiments have been performed on samples machined from Y2-blocks cast with different high-silicon spheroidal graphite irons. Depending on magnesium, silicon, cerium and antimony content, the as-cast microstructure showed various levels of chunky graphite in the central part of the blocks. In contrast, the microstructure of the materials after remelting and resolidification during differential thermal analysis consisted of lamellar or compacted graphite. The formation of chunky graphite in the as-cast microstructure is rationalized using an index or silicon equivalent that has been recently suggested. The differences in the microstructures after differential thermal analysis are discussed in terms of available free magnesium. Emphasis is finally put on the striking differences in characteristic size of the microstructures made of compacted graphite as compared to lamellar graphite and chunky graphite. This leads to tentative conclusions about growth of compacted and chunky graphite which would be worthy of further experimental investigations.
基金supported by two French-Moroccan projects: Volubilis Partenariat Hubert Curien (PHC No.MA 09 205)Projet de Recherches Convention Internationale du CNRS (CNRS-CNRST No.w22572)
文摘We report a simple method for preparing copper（II） molybdate（CuMoO_4） powders via a combustion-like process. A gel was first prepared by the polymerizable complex method, where citric acid was used as a complexing and polymerizing agent and nitric acid was used as an oxidizing agent. The thermal decomposition behavior of the（CuMo）-precursor gel was studied by thermogravimetry–differential thermal analysis（TG–DTA）, Fourier transform infrared spectroscopy（FTIR）, and X-ray diffraction（XRD）. We observed that the crystallization of CuMoO_4 powder was completed at 450°C. The obtained homogeneous powder was composed of grains with sizes in the range from 150 to 500 nm and exhibited a specific surface area of approximately 5 m^2/g. The average grain size increased with increasing annealing temperature. The as-prepared CuMoO_4 crystals showed a strong green photoluminescence emission at room temperature under excitation at 290 nm, which we mainly interpreted on the basis of the Jahn-Teller effect on [MoO_4^（2-）] complex anions. We also observed that the photoluminescence intensity increased with increasing crystallite size.
基金the National Natural Science Foundation of China(NSFC)(22105059,22279112)the Talent Introduction Program of Hebei Agricultural University(YJ201810)+5 种基金the Youth Topnotch Talent Foundation of Hebei Provincial Universities(BJK2022023)the Natural Science Foundation of Hebei Province(B2022203018)the Fok Ying-Tong Education Foundation of China(171064)the Natural Science Foundation of Shandong Province,China(ZR2021QE192)the China Postdoctoral Science Foundation(2018M630747)the 333 Talent Program of Hebei Province(C20221018)for their support。
文摘MoS_(2) is a promising anode material in sodium-ion battery technologies for possessing high theoretical capacity.However,the sluggish Na^(+) diffusion kinetics and low electronic conductivity hinder the promises.Herein,a unique MoS_(2)/FeS_(2)/C heterojunction with abundant defects and hollow structure(MFCHHS)was constructed.The synergy of defect engineering in MoS_(2),FeS_(2),and the carbon layer of MFCHHS with a larger specific surface area provides multiple storage sites of Na^(+)corresponding to the surface-controlled process.The MoS_(2)/FeS_(2)/C heterostructure and rich defects in MoS_(2) and carbon layer lower the Na^(+) diffusion energy barrier.Additionally,the construction of MoS_(2)/FeS_(2) heterojunction promotes electron transfer at the interface,accompanying with excellent conductivity of the carbon layer to facilitate reversible electrochemical reactions.The abundant defects and mismatches at the interface of MoS_(2)/FeS_(2) and MoS_(2)/C heterojunctions could relieve lattice stress and volume change sequentially.As a result,the MFCHHS anode exhibits the high capacity of 613.1 mA h g^(-1)at 0.5 A g^(-1) and 306.1 mA h g^(-1) at 20 A g^(-1).The capacity retention of 85.0%after 1400 cycles at 5.0 A g^(-1) is achieved.The density functional theory(DFT)calculation and in situ transmission electron microscope(TEM),Raman,ex-situ X-ray photon spectroscopy(XPS)studies confirm the low volume change during intercalation/deintercalation process and the efficient Na^(+)storage in the layered structure of MoS_(2) and carbon layer,as well as the defects and heterostructures in MFCHHS.We believe this work could provide an inspiration for constructing heterojunction with abundant defects to foster fast electron and Na^(+) diffusion kinetics,resulting in excellent rate capability and cycling stability.
基金supported by the National Natural Science Foundation of China(Grants No.51902215,91426304,21671195,21805295,51902320,51902319,21875271,and U2004212)the China Postdoctoral Science Foundation(Grant No.2020M680082)+7 种基金the International Partnership Program of Chinese Academy of Sciences(Grants 174433KYSB20190019)the Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang(Grant No.2019R01003)the Ningbo top-talent team program for financial supportsupport from the Swedish Government Strategic Research Area in Materials Science on Functional Materials at Link?ping University(Faculty Grant SFO Mat LiU No.200900971)support of the electron microscopy laboratory in Link?ping(Grant KAW 2015.0043)an Academy Fellow Grant(P.E.,2020.0196)the Swedish Foundation for Strategic Research(SSF)through project funding(EM16-0004)a Research Infrastructure Fellow Grant(RIF 14-0074)。
文摘MAX phases are gaining attention as precursors of two-dimensional MXenes that are intensively pursued in applications for electrochemical energy storage.Here,we report the preparation of V_(2)SnC MAX phase by the molten salt method.V_(2)SnC is investigated as a lithium storage anode,showing a high gravimetric capacity of 490 mAh g−1 and volumetric capacity of 570 mAh cm^(−3) as well as superior rate performance of 95 mAh g^(−1)(110 mAh cm^(−3))at 50 C,surpassing the ever-reported performance of MAX phase anodes.Sup-ported by operando X-ray diffraction and density functional theory,a charge storage mechanism with dual redox reaction is proposed with a Sn-Li(de)alloying reaction that occurs at the edge sites of V_(2)SnC particles where Sn atoms are exposed to the electrolyte followed by a redox reaction that occurs at V_(2)C layers with Li.This study offers promise of using MAX phases with M-site and A-site elements that are redox active as high-rate lithium storage materials.
文摘The study of pickling of the EL21T6 substrate in a nitric acid bath firstly provided knowledge of the influence of the different experimental parameters(concentration of acid,temperature and stirring of the solution)in relation to the etching rate.This experimental part led to the choice of standard pickling(T_(bath)=25℃,moderate stirring(250 rpm),[HNO_(3)]=1.20 mol/L,duration of 2 min)so as to obtain constant removal of material,even after several uses of the pickling bath.SEM observations also confirmed that in these operating conditions,pickling concerns both the grains of the matrix and the precipitates of type Mg3(Nd,Gd),leading to uniform removal of material from the surface.Working from a number of assumptions,thermodynamic and chemical kinetic studies then allowed a pickling mechanism to be proposed and led to obtaining values for the corresponding kinetic parameters(order of reaction,constant of mean rate,activation energy)to be obtained.
基金supported by the National Natural Science Foundation of China (No. 21601148)the Natural Science Foundation of Fujian Province (No. 2017J05090)
文摘Energy storage and conversion have attained significant intere st owing to its important applications that reduce CO2 emission through employing green energy.Some promising technologies are included metalair batteries,metal-sulfur batteries,metal-ion batteries,electrochemical capacitors,etc.Here,metal elements are involved with lithium,sodium,and magnesium.For these devices,electrode materials are of importance to obtain high performance.Two-dimensional(2 D) materials are a large kind of layered structured materials with promising future as energy storage materials,which include graphene,black phosporu s,MXenes,covalent organic frameworks(COFs),2 D oxides,2 D chalcogenides,and others.Great progress has been achieved to go ahead for 2 D materials in energy storage and conversion.More researchers will join in this research field.Under the background,it has motivated us to contribute with a roadmap on ’two-dimensional materials for energy storage and conversion.
基金funding from the European Research Council(ERC)under the European Union’s Horizon 2020 research and innovation program(grant agreement no.714581)supported by the Fundamental Research Funds for the Central Universities(No.YJ201886)+1 种基金the National Natural Science Foundation of China(No.501902215)Sichuan Science and Technology Program(No.2020ZDZX0005)
文摘Computational modeling methods,including molecular dynamics(MD)and Monte Carlo(MC)simulations,and density functional theory(DFT),are receiving booming interests for exploring charge storage mechanisms of electrochemical energy storage devices.These methods can effectively be used to obtain molecular scale local information or provide clear explanations for novel experimental findings that cannot be directly interpreted through experimental investigations.This short review is dedicated to emphasizing recent advances in computational simulation methods for exploring the charge storage mechanisms in typical nanoscale materials,such as nanoporous carbon materials,2 D MXene materials,and metal-organic framework electrodes.Beyond a better understanding of charge storage mechanisms and experimental observations,fast and accurate enough models would be helpful to provide theoretical guidance and experimental basis for the design of new high-performance electrochemical energy storage devices.
文摘This study reports the successful synthesis of supported TiO<sub>2</sub>_Palygorskite nanocomposites by a one-pot dry mechanochemical route. Indeed, the elaboration procedure involved an in-situ reaction between accessories carbonates present in raw fibrous palygorskite clay and titanyl sulfate (TiOSO<sub>4</sub>) precursor under variable grinding conditions, essentially ball/solid matter mass ratio and rotation velocity. This yielded after air annealing at 600%C for 1 h to the immobilization of anatase TiO<sub>2</sub> nanoparticles (≈8 nm of average size) as evidenced by XRD and TEM analyses. Once the conditions of elaboration were optimized, the photocatalytic properties were evaluated under 3 conditions: artificial UV radiation, artificial solar radiation (UV + visible range) and under dynamic solar illumination taking into account the discontinuities of the solar resource. The results allowed the estimation and comparison of the catalyst’s capabilities and showed its ability to work under natural irradiation. The so developed supported photocatalysts TiO<sub>2</sub>/Palygorskite exhibited a good activity towards the removal of Orange G (OG) dye from aqueous media under artificial UV and natural solar radiations.
基金supported by the funding from the European Research Council(ERCAdvanced Grant,ERC-2011-AdG,Project 291543-IONACES)+2 种基金the Materials Institute Carnot Alsace(MICA)from the Direction Générale de l’Armement(DGA)French-German Research Institute of Saint-Louis(ISL)
文摘Fe（3–x）O4 raspberry shaped nanostructures/graphene nanocomposites were synthesized by a one-step polyol-solvothermal method to be tested as electrode materials for Li-ion battery（LIB）. Indeed, Fe（3–x）O4 raspberry shaped nanostructures consist of original oriented aggregates of Fe（3–x）O4 magnetite nanocrystals, ensuring a low oxidation state of magnetite and a hollow and porous structure, which has been easily combined with graphene sheets. The resulting nanocomposite powder displays a very homogeneous spatial distribution of Fe（3–x）O4 nanostructures at the surface of the graphene sheets. These original nanostructures and their strong interaction with the graphene sheets resulted in very small capacity fading upon Li＋ion intercalation. Reversible capacity, as high as 660 m Ah/g, makes this material promising for anode in Li-ion batteries application.
文摘Structural analogues of bicyclic peroxides belonging to the G factors family have been synthesised under Mannieh type conditions, followed by an autoxidation step furnishing exclusively the peroxide. As electron transfer from heine or free iron to peroxide is the first step in the mode of action ofartemisinin -like compound, Fe（fl） induced reduction was studied and the reactivity of the intermediate C-centered radical formed was correlated to the antimalarial activity. Dissociative electron transfer was studied by electrochemistry and allowed the evaluation of the standard reduction potentials and other pertinent thermochemical information. These bicyclic peroxides were evaluated in vitro against Plasmodium falciparum and revealed moderate to good activity.
基金supported by the National Natural Science Foundation of China(Grant No.52072252,No.51902215)Sichuan Science and Technology Program(No.2020ZDZX0005)+4 种基金the Fundamental Research Funds for the Central Universities(YJ201886)the Agence Nationale de la Recherche(Labex STORE-EX)for financial supportsupported by the Leading Innovative and Entrepreneur Team Introduction Program of Zhejiang(Grant No.2019R01003)Ningbo Top-talent Team Program,Ningbo Municipal Bureau of Science and Technology(Grant No.2018A610005)President’s International Fellowship Initiative of CAS(No.2021DE0002).
文摘MXenes are two-dimensional transition metal carbides and/or nitrides with unique physiochemical properties and have attracted extensive interest in numerous fields.However,current MXene synthesis methods are limited by hazardous synthesis conditions,high production costs,or difficulty in largescale production.Therefore,a general,safe,cost-effective,and scalable synthesis method for MXenes is crucial.Here,we report the fast synthesis of MXenes in the open air using a molten salt-shielded synthesis(MS^(3))method,which uses Lewis-acid salts as etchants and a low-melting-point eutectic salt mixture as the reaction medium and shield to prevent MXene oxidation at high temperatures.Carbide and nitride MXenes,including Ti_(3)C_(2)T_(x),Ti_(2)CT_(x),Ti_(3)CNT_(x),and Ti_(4)N_(3)T_(x),were successfully synthesized using the MS^(3)method.We also present the flexibility of the MS^(3)method by scaling the etching process to large batches of 20 and 60 g of Ti_(3)AlC_(2)MAX precursor in one pot.When used as negative electrodes,the prepared MS^(3)-MXenes delivered excellent electrochemical properties for high-rate Li-ion storage.
文摘High volumetric energy density energy storage devices are needed for many applications ranging from miniaturized electronics to electric vehicles[1,2].Two-dimensional(2D)nanosheets,such as graphene,MoS2,and MXene are great candidates for assembling compact sheets[1–5],as their horizontal stacking can achieve interlayer distances close to the diameter of electrolyte ions[1,6].The electrolyte ions confined between interlayers of those materials significantly improve the pore and porous volume utilization,thus achieving compact energy storage realized by ion desolvation[1].
基金This work was supported by the French Agence Nationale de la Recherche(Labex STOREX program)L.Liu is supported by the China Scholarship Council(CSC).
文摘Recently,multivalent aqueous calcium-ion batteries(CIBs)have attracted considerable attention as a possible alternative to Li-ion batteries.However,traditional Ca-ion storage materials show either limited rate capabilities and poor cycle life or insufficient specific capacity.Here,we tackle these limitations by exploring materials having a large interlayer distance to achieve decent specific capacities and one-dimensional architecture with adequate Ca-ion passages that enable rapid reversible(de)intercalation processes.In this work,we report the high-yield,rapid,and low-cost synthesis of 1D metal oxides MV_(3)O_(8)(M=Li,K),CaV_(2)O_(6),and CaV_(6)O_(16)·7H_(2)O(CVO)via a molten salt method.Firstly,using 1D CVO as electrode materials,we show high capacity 205 mA h g^(-1),long cycle life(>97%capacity retention after 200 cycles at 3.0 C),and high-rate performance(117 mA h g^(-1) at 12 C)for Ca-ion(de)intercalation.This work represents a step forward for the development of the molten salt method to synthesize nanomaterials and to help pave the way for the future growth of Ca-ion batteries.
