Layered transition metal oxides have emerged as promising cathode materials for sodium ion batteries.However,irreversible phase transitions cause structural distortion and cation rearrangement,leading to sluggish Na+d...Layered transition metal oxides have emerged as promising cathode materials for sodium ion batteries.However,irreversible phase transitions cause structural distortion and cation rearrangement,leading to sluggish Na+dynamics and rapid capacity decay.In this study,we propose a medium-entropy cathode by simultaneously introducing Fe,Mg,and Li dopants into a typical P2-type Na_(0.75)Ni_(0.25)Mn_(0.75)O_(2)cathode.The modified Na_(0.75)Ni_(0.2125)Mn_(0.6375)Fe_(0.05)Mg_(0.05)Li_(0.05)O_(2)cathode predominantly exhibits a main P2 phase(93.5%)with a minor O3 phase(6.5%).Through spectroscopy techniques and electrochemical investigations,we elucidate the redox mechanisms of Ni^(2+/3+/4+),Mn^(3+/4+),Fe^(3+/4+),and O_(2)-/O_(2)^(n-)during charging/discharging.The medium-entropy doping mitigates the detrimental P2-O_(2)phase transition at high-voltage,replacing it with a moderate and reversible structural evolution(P2-OP4),thereby enhancing structural stability.Consequently,the modified cathode exhibits a remarkable rate capacity of 108.4 mAh·g^(-1)at 10C,with a capacity retention of 99.0%after 200 cycles at 1C,82.5%after 500 cycles at 5C,and 76.7%after 600 cycles at 10C.Furthermore,it also demonstrates superior electrochemical performance at high cutoff voltage of 4.5 V and extreme temperature(55 and 0℃).This work offers solutions to critical challenges in sodium ion batteries cathode materials.展开更多
Nickel-rich(Ni≥90%)layered oxides materials have emerged as a promising candidate for nextgeneration high-energy-density lithium-ion batteries(LIBs).However,their widespread application is hindered by structural fati...Nickel-rich(Ni≥90%)layered oxides materials have emerged as a promising candidate for nextgeneration high-energy-density lithium-ion batteries(LIBs).However,their widespread application is hindered by structural fatigue and lattice oxygen loss.In this work,an epitaxial surface rock-salt nanolayer is successfully developed on the LiNi_(0.9)Co_(0.1)O_(2)sub-surface via heteroatom anchoring utilizing high-valence element molybdenum modification.This in-situ formed conformal buffer phase with a thickness of 1.2 nm effectively suppresses the continuous interphase side-reactions,and thus maintains the excellent structure integrity at high voltage.Furthermore,theoretical calculations indicate that the lattice oxygen reversibility in the anion framework of the optimized sample is obviously enhanced due to the higher content of O 2p states near the Fermi level than that of the pristine one.Meanwhile,the stronger Mo-O bond further reduces cell volume alteration,which improves the bulk structure stability of modified materials.Besides,the detailed charge compensation mechanism suggests that the average oxidation state of Ni is reduced,which induces more active Li+participating in the redox reactions,boosting the cell energy density.As a result,the uniquely designed cathode materials exhibit an extraordinary discharge capacity of 245.4 mAh g^(-1)at 0.1 C,remarkable rate performance of 169.3 mAh g^(-1)at 10 C at 4.5 V,and a high capacity retention of 70.5% after 1000 cycles in full cells at a high cut-off voltage of 4.4 V.This strategy provides an valuable insight into constructing distinctive heterostructure on highperformance Ni-rich layered cathodes for LIBs.展开更多
Layer-structured Ruddlesden–Popper(RP)perovskites(RPPs)with decent stability have captured the imagination of the photovoltaic research community and bring hope for boosting the development of perovskite solar cell(P...Layer-structured Ruddlesden–Popper(RP)perovskites(RPPs)with decent stability have captured the imagination of the photovoltaic research community and bring hope for boosting the development of perovskite solar cell(PSC)technology.However,two-dimensional(2D)or quasi-2D RP PSCs are encountered with some challenges of the large exciton binding energy,blocked charge transport and poor film quality,which restrict their photovoltaic performance.Fortunately,these issues can be readily resolved by rationally designing spacer cations of RPPs.This review mainly focuses on how to design the molecular structures of organic spacers and aims to endow RPPs with outstanding photovoltaic applications.We firstly elucidated the important roles of organic spacers in impacting crystallization kinetics,charge transporting ability and stability of RPPs.Then we brought three aspects to attention for designing organic spacers.Finally,we presented the specific molecular structure design strategies for organic spacers of RPPs aiming to improve photovoltaic performance of RP PSCs.These proposed strategies in this review will provide new avenues to develop novel organic spacers for RPPs and advance the development of RPP photovoltaic technology for future applications.展开更多
Lithium metal batteries(LMBs)with high energy density are impeded by the instability of solid electrolyte interface(SEI)and the uncontrolled growth of lithium(Li)dendrite.To mitigate these challenges,optimizing the SE...Lithium metal batteries(LMBs)with high energy density are impeded by the instability of solid electrolyte interface(SEI)and the uncontrolled growth of lithium(Li)dendrite.To mitigate these challenges,optimizing the SEI structure and Li deposition behavior is the key to stable LMBs.This study novelty proposes a facile synthesis of MgF_(2)/carbon(C)nanocomposite through the mechanochemical reaction between metallic Mg and polytetrafluoroethylene(PTFE)powders,and its modified polypropylene(PP)separator enhances LMB performance.The in-situ formed highly conductive fluorine-doped C species play a crucial role in facilitating ion/electron transport,thereby accelerating electrochemical kinetics and altering Li deposition direction.During cycling,the in-situ reaction between MgF_(2)and Li leads to the formation of LiMg alloy,along with a LiF-rich SEI layer,which reduces the nucleation overpotential and reinforces the interphase strength,leading to homogeneous Li deposition with dendrite-free feature.Benefiting from these merits,the Li metal is densely and uniformly deposited on the MgF_(2)/C@PP separator side rather than on the current collector side.Furthermore,the symmetric cell with MgF_(2)/C@PP exhibits superb Li plating/stripping performance over 2800 h at 1 mA cm^(-2)and 2 mA h cm^(-2).More importantly,the assembled Li@MgF_(2)/C@PPILiFePO4full cell with a low negative/positive ratio of 3.6delivers an impressive cyclability with 82.7%capacity retention over 1400 cycles at 1 C.展开更多
The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure wa...The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure was composed of FCC solid solution,Cr_(23)C_(6) carbide phases,and Mn_(2)SiO_(4) oxy-silicon phase.The relative density,hardness,tensile strength,and elongation of SiC@HEA composites with 1.0 wt.%SiC were 98.5%,HV 358.0,712.3 MPa,and 36.2%,respectively.The core−shell structure had a significant deflecting effect on the cracks.This effect allowed the composites to effectively maintain the excellent plasticity of the matrix.As a result,the core−shell SiC@HEA composites obtained superior strength and plasticity with multiple mechanisms.展开更多
Electric vehicles are pivotal in the global shift toward decarbonizing road transport,with lithium-ion batteries at the heart of this technological evolution.However,the pursuit of batteries capable of extremely fast ...Electric vehicles are pivotal in the global shift toward decarbonizing road transport,with lithium-ion batteries at the heart of this technological evolution.However,the pursuit of batteries capable of extremely fast charging that also satisfy high energy and safety criteria,poses a significant challenge to current lithium-ion batteries technologies.Additionally,the increasing demand for aluminum(Al)and copper(Cu)in electrification,solar energy technologies,and vehicle light-eighting is driving these metals toward near-critical status in the medium term.This study introduces metalized polythylene terephthalate(mPET)polymer films by depositing an Al or Cu thin layer onto two sides of a polyethylene terephthalate film—named mPET/Al and mPET/Cu,as lightweight,cost-effective alternatives to traditional metal current collectors in lithium-ion batteries.We have fabricated current collectors that significantly reduce weight(by 73%),thickness(by 33%),and cost(by 85%)compared with traditional metal foil counterparts.These advancements have the potential to enhance energy density to 280 Wh kg^(-1) at the electrode level under 10-min charging at 6 C.Through testing,including a novel extremely fast charging protocol across various C-rates and long-term cycling(up to 1000 cycles)in different cell configurations,the superior performance of these metalized polymer films has been demonstrated.Notably,mPET/Cu and mPET/Al films exhibited comparable capacities to conventional cells under extremely fast charging,with the mPET cells showing a 27%improvement in energy density at 6 C and maintaining significant energy density after 1000 cycles.This study underscores the potential of mPET films to revolutionize the roll-to-roll battery manufacturing process and significantly advance the performance metrics of lithium-ion batteries in electric vehicles applications.展开更多
Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing co...Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing commercialization efforts using ASTM-certified pathways(e.g.,lipid conversion,Fischer-Tropsch synthesis),production capacities are still inadequate due to limited feedstock supply and high production costs.New conversion technologies that utilize lignocellulosic feedstocks are needed to meet these challenges and satisfy the rapidly growing market.Combining bio-and chemo-catalytic approaches can leverage advantages from both methods,i.e.,high product selectivity via biological conversion,and the capability to build C-C chains more efficiently via chemical catalysis.Herein,conversion routes,catalysis,and processes for such pathways are discussed,while key challenges and meaningful R&D opportunities are identified to guide future research activities in the space.Bio-and chemo-catalytic conversion primarily utilize the carbohydrate fraction of lignocellulose,leaving lignin as a waste product.This makes lignin conversion to SAF critical in order to utilize whole biomass,thereby lowering overall production costs while maximizing carbon efficiencies.Thus,lignin valorization strategies are also reviewed herein with vital research areas identified,such as facile lignin depolymerization approaches,highly integrated conversion systems,novel process configurations,and catalysts for the selective cleavage of aryl C-O bonds.The potential efficiency improvements available via integrated conversion steps,such as combined biological and chemo-catalytic routes,along with the use of different parallel pathways,are identified as key to producing all components of a cost-effective,100%SAF.展开更多
Traditional electrode manufacturing for lithium-ion batteries is well established,reliable,and has already reached high processing speeds and improvements in production costs.For modern electric vehicles,however,the n...Traditional electrode manufacturing for lithium-ion batteries is well established,reliable,and has already reached high processing speeds and improvements in production costs.For modern electric vehicles,however,the need for batteries with high gravimetric and volumetric energy densities at cell level is increasing;and new production concepts are required for this purpose.During the last decade,laser processing of battery materials emerged as a promising processing tool for either improving manufacturing flexibility and product reliability or enhancing battery performances.Laser cutting and welding already reached a high level of maturity and it is obvious that in the near future they will become frequently implemented in battery production lines.This review focuses on laser texturing of electrode materials due to its high potential for significantly enhancing battery performances beyond state-of-the-art.Technical approaches and processing strategies for new electrode architectures and concepts will be presented and discussed with regard to energy and power density requirements.The boost of electrochemical performances due to laser texturing of energy storage materials is currently proven at the laboratory scale.However,promising developments in high-power,ultrafast laser technology may push laser structuring of batteries to the next technical readiness level soon.For demonstration in pilot lines adapted to future cell production,process upscaling regarding footprint area and processing speed are the main issues as well as the economic aspects with regards to CapEx amortization and the benefits resulting from the next generation battery.This review begins with an introduction of the three-dimensional battery and thick film concept,made possible by laser texturing.Laser processing of electrode components,namely current collectors,anodes,and cathodes will be presented.Different types of electrode architectures,such as holes,grids,and lines,were generated;their impact on battery performances are illustrated.The usage of high-energy materials,which are on the threshold of commercialization,is highlighted.Battery performance increase is triggered by controlling lithium-ion diffusion kinetics in liquid electrolyte filled porous electrodes.This review concludes with a discussion of various laser parameter tasks for process upscaling in a new type of extreme manufacturing.展开更多
Herein, a low-cost, biodegradable, and high-performance microwave shielding graphite/starch material was fabricated via constructing a cation-π interaction between ammonium ions and graphite. The graphite flakes and ...Herein, a low-cost, biodegradable, and high-performance microwave shielding graphite/starch material was fabricated via constructing a cation-π interaction between ammonium ions and graphite. The graphite flakes and starch were firstly mixed with distilled water containing ammonium hydroxide to form graphite/starch slurry under an ultrasonic assistant. The cation-π interaction could improve delamination degree and dispersion of graphite in starch matrix. The slurry was first used as a coating material on the surface of wood and paper to develop shielding packages. The effect of coating thickness and coating layers on EM shielding property of the materials was investigated. Second, the composites with a high orientation of graphite were fabricated by compression at high pressures. The electrical conductivity and EM shielding effectiveness(SET) of the materials were greatly enhanced by construction of cation-πinteraction and orientation of graphite. Specifically, the EM SETvalues increased from 56.9 to 66.8 d B for the composites with 50 wt.% graphite and 2.0 mm in thickness by constructing cation-π interaction. The EM SETvalues raised from 17.4 to 66.8 d B via the graphite orientation in the materials with the same components and thickness. The shielding mechanism of the compressed composites with orientation dispersion of graphite was also discussed in comparison to the coating layer with random dispersion of graphite.展开更多
There is an increasing demand for rechargeable batteries in high-performance energy storage systems.The current dominating Li-ion batteries are limited by price,resource availability,as well as their theoretical capac...There is an increasing demand for rechargeable batteries in high-performance energy storage systems.The current dominating Li-ion batteries are limited by price,resource availability,as well as their theoretical capacities.So that the community has started to explore alternative battery chemistries.As a promising multivalent battery type,rechargeable magnesium batteries(RMBs)have attracted increasing attention because of high safety,high volumetric energy density,and low cost thanks to abundant resource of Mg.However,the development of high-performance anodes is still hampered by formation of passivating layers on the Mg surface.Additionally,dendrites can also grow under certain conditions with pure Mg anodes,which requires further studies for reliable operation window and substitutes.Therefore,this review specifically aims to provide an overview on the often overlooked yet very important anode materials of RMBs,with the hope to inspire more attention and research efforts for the achievement of over-all better performance of future RMBs.c 2020 Published by Elsevier B.V.on behalf of Chongqing University.展开更多
Herein, the electrochemical performance and the mechanism of potassium insertion/deinsertion in orthorhombic V_(2)O_(5) nanoparticles are studied. The V2O5 electrode displays an initial potassiation/depotassiation cap...Herein, the electrochemical performance and the mechanism of potassium insertion/deinsertion in orthorhombic V_(2)O_(5) nanoparticles are studied. The V2O5 electrode displays an initial potassiation/depotassiation capacity of 200 mAh g^(−1)/217 mAh g^(−1) in the voltage range 1.5–4.0 V vs. K^(+)/K at C/12 rate, suggesting fast kinetics for potassium insertion/deinsertion. However, the capacity quickly fades during cycling, reaching 54 mAh g^(−1) at the 31st cycle. Afterwards, the capacity slowly increases up to 80 mAh g^(−1) at the 200th cycle. The storage mechanism upon K ions insertion into V2O5 is elucidated. In operando synchrotron diffraction reveals that V_(2)O_(5) first undergoes a solid solution to form K_(0.6)V_(2)O_(5) phase and then, upon further K ions insertion, it reveals coexistence of a solid solution and a two-phase reaction. During K ions deinsertion, the coexistence of solid solution and the two-phase reaction is identified together with an irreversible process. In operando XAS confirms the reduction/oxidation of vanadium during the K insertion/extraction with some irreversible contributions. This is consistent with the results obtained from synchrotron diffraction, ex situ Raman, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Moreover, ex situ XPS confirms the “cathode electrolyte interphase” (CEI) formation on the electrode and the decomposition of CEI film during cycling.展开更多
Density functional methods have been used for the calculation of electronic structures, electronic transitions, vertical electron affinities and intermolecular reorganization energies for tri-aryl substituted dibenzot...Density functional methods have been used for the calculation of electronic structures, electronic transitions, vertical electron affinities and intermolecular reorganization energies for tri-aryl substituted dibenzothiophenes. These model compounds were then compared to the predicted values for dibenzo[b,d]thiophen-2-yltriphenylsilane (DBTSI 2) and to dibenzo[b,d]thiophene-2,8-diylbis(diphenylphosphine oxide) (PO15), known electron transport molecules. The results indicate that these model compounds can be used in a blue OLED system.展开更多
Objective.Laser-treated surfaces for ventricular assist devices.Impact Statement.This work has scientific impact since it proposes a biofunctional surface created with laser processing in bioinert titanium.Introductio...Objective.Laser-treated surfaces for ventricular assist devices.Impact Statement.This work has scientific impact since it proposes a biofunctional surface created with laser processing in bioinert titanium.Introduction.Cardiovascular diseases are the world’s leading cause of death.An especially debilitating heart disease is congestive heart failure.Among the possible therapies,heart transplantation and mechanical circulatory assistance are the main treatments for its severe form at a more advanced stage.The development of biomaterials for ventricular assist devices is still being carried out.Although polished titanium is currently employed in several devices,its performance could be improved by enhancing the bioactivity of its surface.Methods.Aiming to improve the titanium without using coatings that can be detached,this work presents the formation of laser-induced periodic surface structures with a topology suitable for cell adhesion and neointimal tissue formation.The surface was modified by femtosecond laser ablation and cell adhesion was evaluated in vitro by using fibroblast cells.Results.The results indicate the formation of the desired topology,since the cells showed the appropriate adhesion compared to the control group.Scanning electron microscopy showed several positive characteristics in the cells shape and their surface distribution.The in vitro results obtained with different topologies point that the proposed LIPSS would provide enhanced cell adhesion and proliferation.Conclusion.The laser processes studied can create new interactions in biomaterials already known and improve the performance of biomaterials for use in ventricular assist devices.展开更多
This paper presents a systematic investigation of the microstructure and magnetocaloric properties of melt-extracted Sm_(20)Gd_(20)Dy_(20)Co_(20)Al_(20)high-entropy microwires.The fabricated wires exhibited an amorpho...This paper presents a systematic investigation of the microstructure and magnetocaloric properties of melt-extracted Sm_(20)Gd_(20)Dy_(20)Co_(20)Al_(20)high-entropy microwires.The fabricated wires exhibited an amorphous structure,and the temperature interval of the undercooled liquid AT was 45 K.The microwires underwent a second-order magnetic transition from a ferromagnetic to a paramagnetic state near the Curie temperature(T_(C)=52 K),The maximum magnetic entropy change(-ΔS_M^(max)),the relative cooling power and the refrigeration capacity reached 6.34 J·kg^(-1)·K^(-1).422.09 J·kg^(-1)and 332.94 J·kg^(-1),respectively,under a magnetic field change of 5 T.In addition,the temperature-averaged entropy changes with two temperature lifts(3 and 10 K)were 6.32 and 6.27 J·kg^(-1)·K^(-1),respectively.The good magnetocalorie performance highlights the significant potential for the Sm_(20)Gd_(20)Dy_(20)Co_(20)Al_(20)microwires to be used as magnetic refrigerant materials in low-temperature region applications.This work will serve as a valuable reference for future investigations on low-temperature high-entropy magnetocaloric materials.展开更多
In order to achieve combined mechanical and electrical properties,multi-walled carbon nanotubes(MWCNTs)reinforced Cu/Ti_(3)SiC_(2)/C nanocomposites were further processed by high-pressure torsion(HPT).The maximum micr...In order to achieve combined mechanical and electrical properties,multi-walled carbon nanotubes(MWCNTs)reinforced Cu/Ti_(3)SiC_(2)/C nanocomposites were further processed by high-pressure torsion(HPT).The maximum microhardness values of central and edge from the composites with 1 wt.%MWCNTs reached HV 130.0 and HV 363.5,which were 43.9%and 39.5%higher than those of the original samples,respectively.With the same content of MWCNTs,its electrical conductivity achieved 3.42×10^(7) S/m,which was increased by 78.1%compared with that of original samples.The synergistic improvement of mechanical and electrical properties is attributed to the obtained microstructure with increased homogenization and refinement,as well as improved interfacial bonding and reduced porosity.The strengthening mechanisms include dispersion and refinement strengthening for mechanical properties,as well as reduced electron scattering for electrical properties.展开更多
In order to obtain Mg alloys with fine microstructures and high mechanical performances,a novel friction-based processing method,name as“constrained friction processing(CFP)”,was investigated.Via CFP,defect-free Mg-...In order to obtain Mg alloys with fine microstructures and high mechanical performances,a novel friction-based processing method,name as“constrained friction processing(CFP)”,was investigated.Via CFP,defect-free Mg-Zn-Ca rods with greatly refined grains and high mechanical properties were produced.Compared to the previous as-cast microstructure,the grain size was reduced from more than 1 mm to around 4μm within 3 s by a single process cycle.The compressive yield strength was increased by 350%while the ultimate compressive strength by 53%.According to the established material flow behaviors by“tracer material”,the plastic material was transported by shear deformation.From the base material to the rod,the material experienced three stages,i.e.deformation by the tool,upward flow with additional tilt,followed by upward transportation.The microstructural evolution was revealed by“stop-action”technique.The microstructural development at regions adjacent to the rod is mainly controlled by twinning,dynamic recrystallization(DRX)as well as particle stimulated nucleation,while that within the rod is related to DRX combined with grain growth.展开更多
This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The...This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The addition of non-halogen flame retardants(FRs)including aluminum trihydroxide(ATH),triphenyl phosphate(TPP),and diammonium phosphate(DAP)leads to markedly enhanced thermal sta-bility and fire resistance of the PU/nSiO_(2)/FRs nanocomposites,resulting in achieving UL-94 HB standard.In particular,the nanocomposites met the UL-94 V-0 criteria thanks to the inclusion of DAP at 25 phr.The LOI value of the nanocomposites reached 26%which is much higher than that of PU/nSiO_(2)nanocompos-ite,about 20%.In order to further understand the fire-proof mechanism,the residue char layer remaining of the PU/nSiO_(2)/FRs nanocomposites after being burned was also investigated by scanning electron mi-croscopy(SEM)and Fourier transform infrared(FTIR).In addition,the microstructure,thermal stability,thermal conductivity,and mechanical properties of nanocomposites were also evaluated in this study.展开更多
The numerical simulation of arc was carried out for both conventional melt inert gas(MIG)welding and ultrasonic assisted melt inert gas(U-MIG)welding.Based on the model established by Fluent,the arc shape,temperature ...The numerical simulation of arc was carried out for both conventional melt inert gas(MIG)welding and ultrasonic assisted melt inert gas(U-MIG)welding.Based on the model established by Fluent,the arc shape,temperature field,and potential distribution were simulated.The study found that the shape of the arc changed when ultrasonic was added radially;the high-temperature area of the arc stretched,and the temperature peak increased.But as the current increased,the increase in temperature decreased.In addition,under the same conditions,the potential of U-MIG decreased and the pressure on the workpiece increased.To verify the accuracy of the simulation results,welding experiments under identical conditions were carried out,and a high-speed camera was used to collect dynamic pictures of the arc.The simulation results were in a favorable agreement with the experimental results,which provided a certain reference value for ultrasonic assisted arc welding.展开更多
Lithium metal(LM)is a promising anode for next-generation batteries due to its high theoretical capacity and low electrode potential.Nonetheless,side reactions,volume change,and unwanted lithium dendrite growth seriou...Lithium metal(LM)is a promising anode for next-generation batteries due to its high theoretical capacity and low electrode potential.Nonetheless,side reactions,volume change,and unwanted lithium dendrite growth seriously limit the practical application of LM.Herein,with the aid of a hard template approach,a novel lithiophilic CoF_(2)-carbon hollow sphere(CoF_(2)@C-HS)composite material is successfully prepared via a facile in-situ fluorination and etching strategy.The lithiophilic CoF_(2) acts as nucleation sites to reduce nucleation overpotential as well as induces the spatial Li deposition and the formation of LiFrich solid electrolyte interphase(SEI),and the hollow carbon matrix can enhance the electrical conductivity and offer free space for LM deposition.Theoretical simulations reveal that the synergistic effect of lithiophilic CoF_(2) and hollow carbon matrix homogenizes the electric field distribution and Li~+flux.Benefiting from these advantages,the CoF_(2)@C-HS-modified copper substrate electrode delivers an enhanced Coulombic efficiency(CE)of 93.7%for 280 cycles at 1 mA cm^(-2)and 1 mA h cm^(-2).The symmetrical cell using CoF_(2)@C-HS can stably cycle more than 1800 h with a low voltage hysteresis of 11 mV at a current density of 0.5 MA cm^(-2)and an areal capacity of 0.5 mA h cm^(-2).Moreover,the Li@CoF_(2)@C-HS composite anode enables more than 300 stable cycles at 1 C with a capacity retention of 95%in LiFePO_(4)-based full cell and 110 stable cycles at 1 C in LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)-based highvoltage full cell.This work might shed a new light on designing lithiophilic hosts to spatially confine LM deposition,realizing dendrite-free LM anodes and the practical applications of LM batteries.展开更多
The evaluation of plant-based feedstocks is an important aspect of biorefining.Nicotiana glauca is a solanaceous,non-food crop that produces large amounts of biomass and is well adapted to grow in suboptimal condition...The evaluation of plant-based feedstocks is an important aspect of biorefining.Nicotiana glauca is a solanaceous,non-food crop that produces large amounts of biomass and is well adapted to grow in suboptimal conditions.In the present article,compatible sequential solvent extractions were applied to N.glauca leaves to enable the generation of enriched extracts containing higher metabolite content comparing to direct leaf extracts.Typically,between 60 to 100 metabolite components were identified within the fractions.The occurrence of plant fatty acids,fatty acid alcohols,alkanes,sterols and terpenoids was detected by gas liquid chromatography-mass spectrometry(GC-MS)and metabolite identification was confirmed by comparison of physico-chemical properties displayed by available authentic standards.Collectively,co-products such waxes,oils,fermentable sugars,and terpenoids were all identified and quantified.The enriched fractions of N.glauca revealed a high level of readily extractable hydrocarbons,oils and high value co-products.In addition,the saccharification yield and cell wall composition analyses in the stems revealed the potential of the residue material as a promising lignocellulosic substrate for the production of fermentable sugars.In conclusion a multifractional cascade for valuable compounds/commodities has been development,that uses N.glauca biomass.These data have enabled the evaluation of N.glauca material as a potential feedstock for biorefining.展开更多
基金supported by the National Natural Science Foundation of China(No.21805018)by Sichuan Science and Technology Program(Nos.2022ZHCG0018,2023NSFSC0117 and 2023ZHCG0060)Yibin Science and Technology Program(No.2022JB005)and China Postdoctoral Science Foundation(No.2022M722704).
文摘Layered transition metal oxides have emerged as promising cathode materials for sodium ion batteries.However,irreversible phase transitions cause structural distortion and cation rearrangement,leading to sluggish Na+dynamics and rapid capacity decay.In this study,we propose a medium-entropy cathode by simultaneously introducing Fe,Mg,and Li dopants into a typical P2-type Na_(0.75)Ni_(0.25)Mn_(0.75)O_(2)cathode.The modified Na_(0.75)Ni_(0.2125)Mn_(0.6375)Fe_(0.05)Mg_(0.05)Li_(0.05)O_(2)cathode predominantly exhibits a main P2 phase(93.5%)with a minor O3 phase(6.5%).Through spectroscopy techniques and electrochemical investigations,we elucidate the redox mechanisms of Ni^(2+/3+/4+),Mn^(3+/4+),Fe^(3+/4+),and O_(2)-/O_(2)^(n-)during charging/discharging.The medium-entropy doping mitigates the detrimental P2-O_(2)phase transition at high-voltage,replacing it with a moderate and reversible structural evolution(P2-OP4),thereby enhancing structural stability.Consequently,the modified cathode exhibits a remarkable rate capacity of 108.4 mAh·g^(-1)at 10C,with a capacity retention of 99.0%after 200 cycles at 1C,82.5%after 500 cycles at 5C,and 76.7%after 600 cycles at 10C.Furthermore,it also demonstrates superior electrochemical performance at high cutoff voltage of 4.5 V and extreme temperature(55 and 0℃).This work offers solutions to critical challenges in sodium ion batteries cathode materials.
基金financially supported by the National Natural Science Foundation of China(No.52202228,52402298)funded by the Science Research Project of Hebei Education Department(No.BJK2022011)+3 种基金the Central Funds Guiding the Local Science and Technology Development of Hebei Province(No.236Z4404G)the Beijing Tianjin Hebei Basic Research Cooperation Special Project(No.E2024202273)the Science and Technology Correspondent Project of Tianjin(24YDTPJC00240)supported by the U.S.Department of Energy’s Office of Science,Office of Basic Energy Science,Materials Sciences and Engineering Division。
文摘Nickel-rich(Ni≥90%)layered oxides materials have emerged as a promising candidate for nextgeneration high-energy-density lithium-ion batteries(LIBs).However,their widespread application is hindered by structural fatigue and lattice oxygen loss.In this work,an epitaxial surface rock-salt nanolayer is successfully developed on the LiNi_(0.9)Co_(0.1)O_(2)sub-surface via heteroatom anchoring utilizing high-valence element molybdenum modification.This in-situ formed conformal buffer phase with a thickness of 1.2 nm effectively suppresses the continuous interphase side-reactions,and thus maintains the excellent structure integrity at high voltage.Furthermore,theoretical calculations indicate that the lattice oxygen reversibility in the anion framework of the optimized sample is obviously enhanced due to the higher content of O 2p states near the Fermi level than that of the pristine one.Meanwhile,the stronger Mo-O bond further reduces cell volume alteration,which improves the bulk structure stability of modified materials.Besides,the detailed charge compensation mechanism suggests that the average oxidation state of Ni is reduced,which induces more active Li+participating in the redox reactions,boosting the cell energy density.As a result,the uniquely designed cathode materials exhibit an extraordinary discharge capacity of 245.4 mAh g^(-1)at 0.1 C,remarkable rate performance of 169.3 mAh g^(-1)at 10 C at 4.5 V,and a high capacity retention of 70.5% after 1000 cycles in full cells at a high cut-off voltage of 4.4 V.This strategy provides an valuable insight into constructing distinctive heterostructure on highperformance Ni-rich layered cathodes for LIBs.
基金funding from National Science Foundation of China(52202337 and 22178015)the Young Taishan Scholars Program of Shandong Province(tsqn202211082)+1 种基金Natural Science Foundation of Shandong Province(ZR2023MB051)Independent Innovation Research Project of China University of Petroleum(East China)(22CX06023A).
文摘Layer-structured Ruddlesden–Popper(RP)perovskites(RPPs)with decent stability have captured the imagination of the photovoltaic research community and bring hope for boosting the development of perovskite solar cell(PSC)technology.However,two-dimensional(2D)or quasi-2D RP PSCs are encountered with some challenges of the large exciton binding energy,blocked charge transport and poor film quality,which restrict their photovoltaic performance.Fortunately,these issues can be readily resolved by rationally designing spacer cations of RPPs.This review mainly focuses on how to design the molecular structures of organic spacers and aims to endow RPPs with outstanding photovoltaic applications.We firstly elucidated the important roles of organic spacers in impacting crystallization kinetics,charge transporting ability and stability of RPPs.Then we brought three aspects to attention for designing organic spacers.Finally,we presented the specific molecular structure design strategies for organic spacers of RPPs aiming to improve photovoltaic performance of RP PSCs.These proposed strategies in this review will provide new avenues to develop novel organic spacers for RPPs and advance the development of RPP photovoltaic technology for future applications.
基金financially supported by the Natural Science Foundation of China(52277218)the Hubei Provincial Natural Science Foundation of China(2024AFA094)+1 种基金the Excellent Discipline Cultivation Project by JHUN(2023XKZ009)the Graduate Student Innovation Fund of JHUN(KYCXJJ202422).
文摘Lithium metal batteries(LMBs)with high energy density are impeded by the instability of solid electrolyte interface(SEI)and the uncontrolled growth of lithium(Li)dendrite.To mitigate these challenges,optimizing the SEI structure and Li deposition behavior is the key to stable LMBs.This study novelty proposes a facile synthesis of MgF_(2)/carbon(C)nanocomposite through the mechanochemical reaction between metallic Mg and polytetrafluoroethylene(PTFE)powders,and its modified polypropylene(PP)separator enhances LMB performance.The in-situ formed highly conductive fluorine-doped C species play a crucial role in facilitating ion/electron transport,thereby accelerating electrochemical kinetics and altering Li deposition direction.During cycling,the in-situ reaction between MgF_(2)and Li leads to the formation of LiMg alloy,along with a LiF-rich SEI layer,which reduces the nucleation overpotential and reinforces the interphase strength,leading to homogeneous Li deposition with dendrite-free feature.Benefiting from these merits,the Li metal is densely and uniformly deposited on the MgF_(2)/C@PP separator side rather than on the current collector side.Furthermore,the symmetric cell with MgF_(2)/C@PP exhibits superb Li plating/stripping performance over 2800 h at 1 mA cm^(-2)and 2 mA h cm^(-2).More importantly,the assembled Li@MgF_(2)/C@PPILiFePO4full cell with a low negative/positive ratio of 3.6delivers an impressive cyclability with 82.7%capacity retention over 1400 cycles at 1 C.
基金supported by Key Laboratory of Infrared Imaging Materials and Detectors,Shanghai Institute of Technical Physics,Chinese Academy of Sciences(No.IIMDKFJJ-21-10)China Postdoctoral Science Foundation(No.2018T110993)。
文摘The novel core−shell SiC@CoCrFeNiMn high-entropy alloy(HEA)matrix composites(SiC@HEA)were successfully prepared via mechanical ball milling and vacuum hot-pressing sintering(VHPS).After sintering,the microstructure was composed of FCC solid solution,Cr_(23)C_(6) carbide phases,and Mn_(2)SiO_(4) oxy-silicon phase.The relative density,hardness,tensile strength,and elongation of SiC@HEA composites with 1.0 wt.%SiC were 98.5%,HV 358.0,712.3 MPa,and 36.2%,respectively.The core−shell structure had a significant deflecting effect on the cracks.This effect allowed the composites to effectively maintain the excellent plasticity of the matrix.As a result,the core−shell SiC@HEA composites obtained superior strength and plasticity with multiple mechanisms.
文摘Electric vehicles are pivotal in the global shift toward decarbonizing road transport,with lithium-ion batteries at the heart of this technological evolution.However,the pursuit of batteries capable of extremely fast charging that also satisfy high energy and safety criteria,poses a significant challenge to current lithium-ion batteries technologies.Additionally,the increasing demand for aluminum(Al)and copper(Cu)in electrification,solar energy technologies,and vehicle light-eighting is driving these metals toward near-critical status in the medium term.This study introduces metalized polythylene terephthalate(mPET)polymer films by depositing an Al or Cu thin layer onto two sides of a polyethylene terephthalate film—named mPET/Al and mPET/Cu,as lightweight,cost-effective alternatives to traditional metal current collectors in lithium-ion batteries.We have fabricated current collectors that significantly reduce weight(by 73%),thickness(by 33%),and cost(by 85%)compared with traditional metal foil counterparts.These advancements have the potential to enhance energy density to 280 Wh kg^(-1) at the electrode level under 10-min charging at 6 C.Through testing,including a novel extremely fast charging protocol across various C-rates and long-term cycling(up to 1000 cycles)in different cell configurations,the superior performance of these metalized polymer films has been demonstrated.Notably,mPET/Cu and mPET/Al films exhibited comparable capacities to conventional cells under extremely fast charging,with the mPET cells showing a 27%improvement in energy density at 6 C and maintaining significant energy density after 1000 cycles.This study underscores the potential of mPET films to revolutionize the roll-to-roll battery manufacturing process and significantly advance the performance metrics of lithium-ion batteries in electric vehicles applications.
基金supported by the Center for Bioenergy Innovation(CBI)supported by the Office of Biological and Environmental Research in the DOE Office of Science and led by Oak Ridge National Laboratory.Oak Ridge National Laboratory is managed by UT-Battelle,LLC for the US DOE under Contract Number DE-AC05-00OR22725+2 种基金authored in part by the Na-tional Renewable Energy Laboratory,operated by Alliance for Sustainable Energy,LLC,for the U.S.Department of Energy(DOE)under Contract No.DE-LC-000L054provided by the U.S.Department of Energy(DOE),Office of Energy Efficiency and Renewable Energy(EERE),and Bioenergy Technologies Office(BETO)at the Pacific Northwest National Laboratory(PNNL)under Contract No.DE-AC05-76RL01830supported by Laboratory Directed Research and Development(LDRD)funding from Argonne National Laboratory,provided by the Director,Office of Science,of the U.S.Department of Energy under Contract No.DE-AC02-06CH11357。
文摘Sustainable aviation fuel(SAF)production from biomass and biowaste streams is an attractive option for decarbonizing the aviation sector,one of the most-difficult-to-electrify transportation sectors.Despite ongoing commercialization efforts using ASTM-certified pathways(e.g.,lipid conversion,Fischer-Tropsch synthesis),production capacities are still inadequate due to limited feedstock supply and high production costs.New conversion technologies that utilize lignocellulosic feedstocks are needed to meet these challenges and satisfy the rapidly growing market.Combining bio-and chemo-catalytic approaches can leverage advantages from both methods,i.e.,high product selectivity via biological conversion,and the capability to build C-C chains more efficiently via chemical catalysis.Herein,conversion routes,catalysis,and processes for such pathways are discussed,while key challenges and meaningful R&D opportunities are identified to guide future research activities in the space.Bio-and chemo-catalytic conversion primarily utilize the carbohydrate fraction of lignocellulose,leaving lignin as a waste product.This makes lignin conversion to SAF critical in order to utilize whole biomass,thereby lowering overall production costs while maximizing carbon efficiencies.Thus,lignin valorization strategies are also reviewed herein with vital research areas identified,such as facile lignin depolymerization approaches,highly integrated conversion systems,novel process configurations,and catalysts for the selective cleavage of aryl C-O bonds.The potential efficiency improvements available via integrated conversion steps,such as combined biological and chemo-catalytic routes,along with the use of different parallel pathways,are identified as key to producing all components of a cost-effective,100%SAF.
基金The research to anode material development received funding from the German Research Foundation(DFG,project No.392322200)the development of cathode materials and upscaling strategies was funded by the Federal Ministry of Education and Research(Project NextGen-3DBat,03XP0198F).
文摘Traditional electrode manufacturing for lithium-ion batteries is well established,reliable,and has already reached high processing speeds and improvements in production costs.For modern electric vehicles,however,the need for batteries with high gravimetric and volumetric energy densities at cell level is increasing;and new production concepts are required for this purpose.During the last decade,laser processing of battery materials emerged as a promising processing tool for either improving manufacturing flexibility and product reliability or enhancing battery performances.Laser cutting and welding already reached a high level of maturity and it is obvious that in the near future they will become frequently implemented in battery production lines.This review focuses on laser texturing of electrode materials due to its high potential for significantly enhancing battery performances beyond state-of-the-art.Technical approaches and processing strategies for new electrode architectures and concepts will be presented and discussed with regard to energy and power density requirements.The boost of electrochemical performances due to laser texturing of energy storage materials is currently proven at the laboratory scale.However,promising developments in high-power,ultrafast laser technology may push laser structuring of batteries to the next technical readiness level soon.For demonstration in pilot lines adapted to future cell production,process upscaling regarding footprint area and processing speed are the main issues as well as the economic aspects with regards to CapEx amortization and the benefits resulting from the next generation battery.This review begins with an introduction of the three-dimensional battery and thick film concept,made possible by laser texturing.Laser processing of electrode components,namely current collectors,anodes,and cathodes will be presented.Different types of electrode architectures,such as holes,grids,and lines,were generated;their impact on battery performances are illustrated.The usage of high-energy materials,which are on the threshold of commercialization,is highlighted.Battery performance increase is triggered by controlling lithium-ion diffusion kinetics in liquid electrolyte filled porous electrodes.This review concludes with a discussion of various laser parameter tasks for process upscaling in a new type of extreme manufacturing.
基金financially supported by the National Natural Science Foundation of China(No.52173264)the Natural Scienceof Chongqing(No.cstc2020jcyjmsxmX0401)。
文摘Herein, a low-cost, biodegradable, and high-performance microwave shielding graphite/starch material was fabricated via constructing a cation-π interaction between ammonium ions and graphite. The graphite flakes and starch were firstly mixed with distilled water containing ammonium hydroxide to form graphite/starch slurry under an ultrasonic assistant. The cation-π interaction could improve delamination degree and dispersion of graphite in starch matrix. The slurry was first used as a coating material on the surface of wood and paper to develop shielding packages. The effect of coating thickness and coating layers on EM shielding property of the materials was investigated. Second, the composites with a high orientation of graphite were fabricated by compression at high pressures. The electrical conductivity and EM shielding effectiveness(SET) of the materials were greatly enhanced by construction of cation-πinteraction and orientation of graphite. Specifically, the EM SETvalues increased from 56.9 to 66.8 d B for the composites with 50 wt.% graphite and 2.0 mm in thickness by constructing cation-π interaction. The EM SETvalues raised from 17.4 to 66.8 d B via the graphite orientation in the materials with the same components and thickness. The shielding mechanism of the compressed composites with orientation dispersion of graphite was also discussed in comparison to the coating layer with random dispersion of graphite.
基金the German Research Foundation DFG project(LI 2839/1-1)National Natural Science Foundation of China(51971044)MF acknowledges funding from EU research and innovation framework programme via ttE-MAGIC,project(ID:824066)。
文摘There is an increasing demand for rechargeable batteries in high-performance energy storage systems.The current dominating Li-ion batteries are limited by price,resource availability,as well as their theoretical capacities.So that the community has started to explore alternative battery chemistries.As a promising multivalent battery type,rechargeable magnesium batteries(RMBs)have attracted increasing attention because of high safety,high volumetric energy density,and low cost thanks to abundant resource of Mg.However,the development of high-performance anodes is still hampered by formation of passivating layers on the Mg surface.Additionally,dendrites can also grow under certain conditions with pure Mg anodes,which requires further studies for reliable operation window and substitutes.Therefore,this review specifically aims to provide an overview on the often overlooked yet very important anode materials of RMBs,with the hope to inspire more attention and research efforts for the achievement of over-all better performance of future RMBs.c 2020 Published by Elsevier B.V.on behalf of Chongqing University.
基金This work contributes to the research performed at CELEST(Center for Electrochemical Energy Storage Ulm-Karlsruhe)and was funded by the German Research Foundation(DFG)under Project ID 390874152(POLiS Cluster of Excellence)Our research work has gained benefit from beamtime allocation(2017092405-qfu)at BL04-MSPD at ALBA Synchrotron,Barcelona,Spain and(I-20170977)at PETRA-III beamline P65 at DESY,Hamburg,Germany.The in operando XAS work was performed by using the Biologic potentiostat of PETRA-Ⅲ beamline P02.1.We thank Dr.Francois Fauth from Experiments Division at ALBA for his technical help during synchrotron diffraction measurement.We appreciate Dr.Anna-Lena Hansen(IAM-ESS)for the helpful discussion regarding to the crystal sturcture of V_(2)O_(5).Dr.Kristina Pfeifer(IAM-ESS),Dr.Noha Sabi(IAM-ESS),and Dr.Thomas Bergfeldt(IAM-AWP)are gratefully acknowledged for SEM/EDX,FTIR,and ICP-OES measurements,respectively.The TEM characterization was carried out at the Karlsruhe Nano Micro Facility(KNMF),a Helmholtz research infrastructure operated at the KIT.
文摘Herein, the electrochemical performance and the mechanism of potassium insertion/deinsertion in orthorhombic V_(2)O_(5) nanoparticles are studied. The V2O5 electrode displays an initial potassiation/depotassiation capacity of 200 mAh g^(−1)/217 mAh g^(−1) in the voltage range 1.5–4.0 V vs. K^(+)/K at C/12 rate, suggesting fast kinetics for potassium insertion/deinsertion. However, the capacity quickly fades during cycling, reaching 54 mAh g^(−1) at the 31st cycle. Afterwards, the capacity slowly increases up to 80 mAh g^(−1) at the 200th cycle. The storage mechanism upon K ions insertion into V2O5 is elucidated. In operando synchrotron diffraction reveals that V_(2)O_(5) first undergoes a solid solution to form K_(0.6)V_(2)O_(5) phase and then, upon further K ions insertion, it reveals coexistence of a solid solution and a two-phase reaction. During K ions deinsertion, the coexistence of solid solution and the two-phase reaction is identified together with an irreversible process. In operando XAS confirms the reduction/oxidation of vanadium during the K insertion/extraction with some irreversible contributions. This is consistent with the results obtained from synchrotron diffraction, ex situ Raman, X-ray photoelectron spectroscopy (XPS), and transmission electron microscopy (TEM). Moreover, ex situ XPS confirms the “cathode electrolyte interphase” (CEI) formation on the electrode and the decomposition of CEI film during cycling.
文摘Density functional methods have been used for the calculation of electronic structures, electronic transitions, vertical electron affinities and intermolecular reorganization energies for tri-aryl substituted dibenzothiophenes. These model compounds were then compared to the predicted values for dibenzo[b,d]thiophen-2-yltriphenylsilane (DBTSI 2) and to dibenzo[b,d]thiophene-2,8-diylbis(diphenylphosphine oxide) (PO15), known electron transport molecules. The results indicate that these model compounds can be used in a blue OLED system.
文摘Objective.Laser-treated surfaces for ventricular assist devices.Impact Statement.This work has scientific impact since it proposes a biofunctional surface created with laser processing in bioinert titanium.Introduction.Cardiovascular diseases are the world’s leading cause of death.An especially debilitating heart disease is congestive heart failure.Among the possible therapies,heart transplantation and mechanical circulatory assistance are the main treatments for its severe form at a more advanced stage.The development of biomaterials for ventricular assist devices is still being carried out.Although polished titanium is currently employed in several devices,its performance could be improved by enhancing the bioactivity of its surface.Methods.Aiming to improve the titanium without using coatings that can be detached,this work presents the formation of laser-induced periodic surface structures with a topology suitable for cell adhesion and neointimal tissue formation.The surface was modified by femtosecond laser ablation and cell adhesion was evaluated in vitro by using fibroblast cells.Results.The results indicate the formation of the desired topology,since the cells showed the appropriate adhesion compared to the control group.Scanning electron microscopy showed several positive characteristics in the cells shape and their surface distribution.The in vitro results obtained with different topologies point that the proposed LIPSS would provide enhanced cell adhesion and proliferation.Conclusion.The laser processes studied can create new interactions in biomaterials already known and improve the performance of biomaterials for use in ventricular assist devices.
基金financially supported by the National Natural Science Foundation of China(No.51827801)the support by the Overseas Visiting Study Program of Harbin Institute of Technology。
文摘This paper presents a systematic investigation of the microstructure and magnetocaloric properties of melt-extracted Sm_(20)Gd_(20)Dy_(20)Co_(20)Al_(20)high-entropy microwires.The fabricated wires exhibited an amorphous structure,and the temperature interval of the undercooled liquid AT was 45 K.The microwires underwent a second-order magnetic transition from a ferromagnetic to a paramagnetic state near the Curie temperature(T_(C)=52 K),The maximum magnetic entropy change(-ΔS_M^(max)),the relative cooling power and the refrigeration capacity reached 6.34 J·kg^(-1)·K^(-1).422.09 J·kg^(-1)and 332.94 J·kg^(-1),respectively,under a magnetic field change of 5 T.In addition,the temperature-averaged entropy changes with two temperature lifts(3 and 10 K)were 6.32 and 6.27 J·kg^(-1)·K^(-1),respectively.The good magnetocalorie performance highlights the significant potential for the Sm_(20)Gd_(20)Dy_(20)Co_(20)Al_(20)microwires to be used as magnetic refrigerant materials in low-temperature region applications.This work will serve as a valuable reference for future investigations on low-temperature high-entropy magnetocaloric materials.
基金supported by Key Laboratory of Infrared Imaging Materials and Detectors,Shanghai Institute of Technical Physics,Chinese Academy of Sciences(No.IIMDKFJJ-21-10)China Postdoctoral Science Foundation(No.2018T110993).
文摘In order to achieve combined mechanical and electrical properties,multi-walled carbon nanotubes(MWCNTs)reinforced Cu/Ti_(3)SiC_(2)/C nanocomposites were further processed by high-pressure torsion(HPT).The maximum microhardness values of central and edge from the composites with 1 wt.%MWCNTs reached HV 130.0 and HV 363.5,which were 43.9%and 39.5%higher than those of the original samples,respectively.With the same content of MWCNTs,its electrical conductivity achieved 3.42×10^(7) S/m,which was increased by 78.1%compared with that of original samples.The synergistic improvement of mechanical and electrical properties is attributed to the obtained microstructure with increased homogenization and refinement,as well as improved interfacial bonding and reduced porosity.The strengthening mechanisms include dispersion and refinement strengthening for mechanical properties,as well as reduced electron scattering for electrical properties.
基金the China Scholarship Council for the award of fellowship and funding(No.202006230137)。
文摘In order to obtain Mg alloys with fine microstructures and high mechanical performances,a novel friction-based processing method,name as“constrained friction processing(CFP)”,was investigated.Via CFP,defect-free Mg-Zn-Ca rods with greatly refined grains and high mechanical properties were produced.Compared to the previous as-cast microstructure,the grain size was reduced from more than 1 mm to around 4μm within 3 s by a single process cycle.The compressive yield strength was increased by 350%while the ultimate compressive strength by 53%.According to the established material flow behaviors by“tracer material”,the plastic material was transported by shear deformation.From the base material to the rod,the material experienced three stages,i.e.deformation by the tool,upward flow with additional tilt,followed by upward transportation.The microstructural evolution was revealed by“stop-action”technique.The microstructural development at regions adjacent to the rod is mainly controlled by twinning,dynamic recrystallization(DRX)as well as particle stimulated nucleation,while that within the rod is related to DRX combined with grain growth.
基金funded by the Vietnam National University Ho Chi Minh City(VNU-HCM)under grant number C2022-18-41.
文摘This study focuses on the improvement of the thermal stability and flame-retardant performance of polyurethane(PU)foam by using effective flame-retardant additives and nano silica(nSiO_(2))particles from rice husk.The addition of non-halogen flame retardants(FRs)including aluminum trihydroxide(ATH),triphenyl phosphate(TPP),and diammonium phosphate(DAP)leads to markedly enhanced thermal sta-bility and fire resistance of the PU/nSiO_(2)/FRs nanocomposites,resulting in achieving UL-94 HB standard.In particular,the nanocomposites met the UL-94 V-0 criteria thanks to the inclusion of DAP at 25 phr.The LOI value of the nanocomposites reached 26%which is much higher than that of PU/nSiO_(2)nanocompos-ite,about 20%.In order to further understand the fire-proof mechanism,the residue char layer remaining of the PU/nSiO_(2)/FRs nanocomposites after being burned was also investigated by scanning electron mi-croscopy(SEM)and Fourier transform infrared(FTIR).In addition,the microstructure,thermal stability,thermal conductivity,and mechanical properties of nanocomposites were also evaluated in this study.
基金the National Natural Science Foundation of China(No.51665037)。
文摘The numerical simulation of arc was carried out for both conventional melt inert gas(MIG)welding and ultrasonic assisted melt inert gas(U-MIG)welding.Based on the model established by Fluent,the arc shape,temperature field,and potential distribution were simulated.The study found that the shape of the arc changed when ultrasonic was added radially;the high-temperature area of the arc stretched,and the temperature peak increased.But as the current increased,the increase in temperature decreased.In addition,under the same conditions,the potential of U-MIG decreased and the pressure on the workpiece increased.To verify the accuracy of the simulation results,welding experiments under identical conditions were carried out,and a high-speed camera was used to collect dynamic pictures of the arc.The simulation results were in a favorable agreement with the experimental results,which provided a certain reference value for ultrasonic assisted arc welding.
基金supported by the Natural Science Foundation of China (52277218)the Hubei Provincial Natural Science Foundation of China (2024AFA094)+1 种基金the Excellent Discipline Cultivation Project by JHUN (2023XKZ009)supported by the U.S.Department of Energy,Office of Science,Office of Basic Energy Sciences,Materials Sciences and Engineering Division under contract number DE-AC05-00OR22725。
文摘Lithium metal(LM)is a promising anode for next-generation batteries due to its high theoretical capacity and low electrode potential.Nonetheless,side reactions,volume change,and unwanted lithium dendrite growth seriously limit the practical application of LM.Herein,with the aid of a hard template approach,a novel lithiophilic CoF_(2)-carbon hollow sphere(CoF_(2)@C-HS)composite material is successfully prepared via a facile in-situ fluorination and etching strategy.The lithiophilic CoF_(2) acts as nucleation sites to reduce nucleation overpotential as well as induces the spatial Li deposition and the formation of LiFrich solid electrolyte interphase(SEI),and the hollow carbon matrix can enhance the electrical conductivity and offer free space for LM deposition.Theoretical simulations reveal that the synergistic effect of lithiophilic CoF_(2) and hollow carbon matrix homogenizes the electric field distribution and Li~+flux.Benefiting from these advantages,the CoF_(2)@C-HS-modified copper substrate electrode delivers an enhanced Coulombic efficiency(CE)of 93.7%for 280 cycles at 1 mA cm^(-2)and 1 mA h cm^(-2).The symmetrical cell using CoF_(2)@C-HS can stably cycle more than 1800 h with a low voltage hysteresis of 11 mV at a current density of 0.5 MA cm^(-2)and an areal capacity of 0.5 mA h cm^(-2).Moreover,the Li@CoF_(2)@C-HS composite anode enables more than 300 stable cycles at 1 C with a capacity retention of 95%in LiFePO_(4)-based full cell and 110 stable cycles at 1 C in LiNi_(0.8)Co_(0.1)Mn_(0.1)O_(2)(NCM811)-based highvoltage full cell.This work might shed a new light on designing lithiophilic hosts to spatially confine LM deposition,realizing dendrite-free LM anodes and the practical applications of LM batteries.
基金Open Access funding enabled and organized by Projekt DEALThe research from the MultiBioPro project leading to these results has received funding from the European Union’s Seventh Framework Programme for research,technological development and demonstration under grant agreement 311804Further funding from the BBSRC 21EBTA-Celfacto project is acknowledged by PDF.
文摘The evaluation of plant-based feedstocks is an important aspect of biorefining.Nicotiana glauca is a solanaceous,non-food crop that produces large amounts of biomass and is well adapted to grow in suboptimal conditions.In the present article,compatible sequential solvent extractions were applied to N.glauca leaves to enable the generation of enriched extracts containing higher metabolite content comparing to direct leaf extracts.Typically,between 60 to 100 metabolite components were identified within the fractions.The occurrence of plant fatty acids,fatty acid alcohols,alkanes,sterols and terpenoids was detected by gas liquid chromatography-mass spectrometry(GC-MS)and metabolite identification was confirmed by comparison of physico-chemical properties displayed by available authentic standards.Collectively,co-products such waxes,oils,fermentable sugars,and terpenoids were all identified and quantified.The enriched fractions of N.glauca revealed a high level of readily extractable hydrocarbons,oils and high value co-products.In addition,the saccharification yield and cell wall composition analyses in the stems revealed the potential of the residue material as a promising lignocellulosic substrate for the production of fermentable sugars.In conclusion a multifractional cascade for valuable compounds/commodities has been development,that uses N.glauca biomass.These data have enabled the evaluation of N.glauca material as a potential feedstock for biorefining.
