Based on the functionally graded materials （FGMs） design concept, the laminated-graded graphite/cermets self-lubricating composite was prepared to achieve the integration of mechanical prop- erties and lubrication p...Based on the functionally graded materials （FGMs） design concept, the laminated-graded graphite/cermets self-lubricating composite was prepared to achieve the integration of mechanical prop- erties and lubrication performance of the cermet. The effects of the layer number and thickness of graded structure on residual stresses in the gradient composites were investigated by finite element method （FEM）. From the FEM analyses, the optimal gradient structure design was obtained correspond- ing to the following parameters： the number of graded layers n = 2 and the thickness of graded structure t = I ram. According to the optimum design, a graded graphite/cermets self-lubricating material with two layers was fabricated by a typical powder metallurgy technique. Compared with the homogenous graphite/cermets composite, the surface hardness and indentation fracture toughness of graded compos- ite were increased by approximately 15.9% and 6.3%, respectively. The results of X-ray diffraction （XRD） stress measurement identified the existence of residual compressive stress on the surface of graded com- posite. Additionally, the friction and wear tests revealed that the wear resistance of the graphite/cermets self-lubricating composite was improved significantly via the graded structural design, whereas the coefficient of friction changed slightly.展开更多
Graphite,encompassing both natural graphite and synthetic graphite,and graphene,have been extensively utilized and investigated as anode materials and additives in lithium-ion batteries(LIBs).In the pursuit of carbon ...Graphite,encompassing both natural graphite and synthetic graphite,and graphene,have been extensively utilized and investigated as anode materials and additives in lithium-ion batteries(LIBs).In the pursuit of carbon neutrality,LIBs are expected to play a pivotal role in reducing CO_(2)emissions by decreasing reliance on fossil fuels and enabling the integration of renewable energy sources.Owing to their technological maturity and exceptional electrochemical performance,the global production of graphite and graphene for LIBs is projected to continue expanding.Over the past decades,numerous researchers have concentrated on reducing the material and energy input whilst optimising the electrochemical performance of graphite and graphene,through novel synthesis methods and various modifications at the laboratory scale.This review provides a comprehensive examination of the manufacturing methods,environmental impact,research progress,and challenges associated with graphite and graphene in LIBs from an industrial perspective,with a particular focus on the carbon footprint of production processes.Additionally,it considers emerging challenges and future development directions of graphite and graphene,offering significant insights for ongoing and future research in the field of green LIBs.展开更多
Fine-grained nuclear graphite is a key material in high-temperature gas-cooled reactors(HTGRs).During air ingress accidents,core graphite components undergo severe oxidation,threatening structural integrity.Therefore,...Fine-grained nuclear graphite is a key material in high-temperature gas-cooled reactors(HTGRs).During air ingress accidents,core graphite components undergo severe oxidation,threatening structural integrity.Therefore,understanding the oxidation behavior of nuclear graphite is essential for reactor safety.The influence of oxidation involves multiple factors,including temperature,sample size,oxidant,impurities,filler type and size,etc.The size of the filler particles plays a crucial role in this study.Five ultrafine-and superfine-grained nuclear graphite samples(5.9-34.4μm)are manufactured using identical raw materials and manufacturing processes.Isothermal oxidation tests conducted at 650℃-750℃ are used to study the oxidation behavior.Additionally,comprehensive characterization is performed to analyze the crystal structure,surface morphology,and nanoscale to microscale pore structure of the samples.Results indicate that oxidation behavior cannot be predicted solely based on filler grain size.Reactive site concentration,characterized by active surface area,dominates the chemical reaction kinetics,whereas pore tortuosity,quantified by the structural parameterΨ,plays a key role in regulating oxidant diffusion.These findings clarify the dual role of microstructure in oxidation mechanisms and establish a theoretical and experimental basis for the design of high-performance nuclear graphite capable of long-term service in high-temperature gas-cooled reactors.展开更多
In order to effectively prevent the contamination of carbon particle volatiles during high-purity SiC crystals are prepared using the physical vapor transport(PVT)method in ultra-high temperature environments(T³2...In order to effectively prevent the contamination of carbon particle volatiles during high-purity SiC crystals are prepared using the physical vapor transport(PVT)method in ultra-high temperature environments(T³2000℃),this study innovatively attempts to protect graphite materials with SiC reinforced pyrolytic graphite(PyG)coating.It is discovered by preparing the SiC particle layer,the degree of graphitization and stability of PyG coating can be improved.The corrosion test results demonstrated that the SiC reinforced PyG coating can maintain an intact coating with a high graphitization degree after the SiC vapour corrosion test of 2050℃-120 h.Conversely,the samples with and without PyG coating reveal porous and eroded surfaces.Furthermore,following the SiC vapour corrosion test,the PyG coating sample’s integral ratio of D-band and G-band(I_(D)/I_(G))of Raman spectrum test data,reduced by 6.5%,while the SiC reinforced PyG coating decreased by 17.2%,indicating its excellent corrosion resistance.The application of SiC reinforced pyrolytic graphite coating in preparing the SiC single crystal might received a theoretical foundation according to this work.展开更多
To enhance the electrochemical performance of lithium-ion battery anodes with higher silicon content,it is essential to engineer their microstructure for better lithium-ion transport and mitigated volume change as wel...To enhance the electrochemical performance of lithium-ion battery anodes with higher silicon content,it is essential to engineer their microstructure for better lithium-ion transport and mitigated volume change as well.Herein,we suggest an effective approach to control the micropore structure of silicon oxide(SiO_(x))/artificial graphite(AG)composite electrodes using a perforated current collector.The electrode features a unique pore structure,where alternating high-porosity domains and low-porosity domains markedly reduce overall electrode resistance,leading to a 20%improvement in rate capability at a 5C-rate discharge condition.Using microstructure-resolved modeling and simulations,we demonstrate that the patterned micropore structure enhances lithium-ion transport,mitigating the electrolyte concentration gradient of lithium-ion.Additionally,perforating current collector with a chemical etching process increases the number of hydrogen bonding sites and enlarges the interface with the SiO_(x)/AG composite electrode,significantly improving adhesion strength.This,in turn,suppresses mechanical degradation and leads to a 50%higher capacity retention.Thus,regularly arranged micropore structure enabled by the perforated current collector successfully improves both rate capability and cycle life in SiO_(x)/AG composite electrodes,providing valuable insights into electrode engineering.展开更多
Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphi...Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphite.This study utilizes the porous“defect advantage”of a cathode carbon block matrix to prepare silicon-doped and asphalt-coated detoxified and purified waste graphitization cathode carbon blocks for use as high-performance silicon/carbon composite anode materials.The results show that the uniformly silicondoped silicon/carbon composite material features a unique amorphous carbon-encapsulated“locked silicon”structure,which effectively addresses issues such as cathode volume expansion,excessive growth of the solid electrolyte interphase(SEI)film,and poor electrical contact between active materials.Consequently,electrochemical performance is enhanced.After assembly in a half-cell,the PSCC/10%Si@C(purified waste graphitization cathode carbon/10%Si@C)material exhibits optimal electrochemical stability,with an initial charging specific capacity of 514.5 mAh/g at 0.1 C(1 C=170 mA/g)and a capacity retention rate of 95.1%after 100 cycles.At a charge rate of 2.0 C,a specific capacity of 216.9 mAh/g is achieved.This technology provides a new pathway for the economical and high-value utilization of waste cathode carbon blocks and the development of low-cost,high-performance anode materials.展开更多
We adopted the solution impregnation route with aluminum dihydrogen phosphate solution as liquid medium for effective surface modification on graphite substrate.The mass ratio of graphite to Al(H_(2)PO_(4))_(3) change...We adopted the solution impregnation route with aluminum dihydrogen phosphate solution as liquid medium for effective surface modification on graphite substrate.The mass ratio of graphite to Al(H_(2)PO_(4))_(3) changed from 0.5:1 to 4:1,and the impregnation time changed from 1 to 7 h.The typical composite phase change thermal storage materials doped with the as-treated graphite were fabricated using form-stable technique.To investigate the oxidation and anti-oxidation behavior of the impregnated graphite at high temperatures,the samples were put into a muffle furnace for a cyclic heat test.Based on SEM,EDS,DSC techniques,analyses on the impregnated technique suggested an optimized processing conditions of a 3 h impregnation time with the ratio of graphite:Al(H_(2)PO_(4))_(3) as 1:3 for graphite impregnation treatment.Further investigations on high-temperature phase change heat storage materials doped by the treated graphite suggested excellent oxidation resistance and thermal cycling performance.展开更多
Lithium-ion batteries(LIBs)are an electrochemical energy storage technology that has been widely used for portable electrical devices,electric vehicles,and grid storage,etc.To satisfy the demand for user convenience e...Lithium-ion batteries(LIBs)are an electrochemical energy storage technology that has been widely used for portable electrical devices,electric vehicles,and grid storage,etc.To satisfy the demand for user convenience especially for electric vehicles,the development of a fast-charging technology for LIBs has become a critical focus.In commercial LIBs,the slow kinetics of Li+intercalation into the graphite anode from the electrolyte solution is known as the main restriction for fast-charging.We summarize the recent advances in obtaining fast-charging graphite-based anodes,mainly involving modifications of the electrolyte solution and graphite anode.Specifically,strategies for increasing the ionic conductivity and regulating the Li+solvation/desolvation state in the electrolyte solution,as well as optimizing the fabrication and the intrinsic activity of graphite-based anodes are discussed in detail.This review considers practical ways to obtain fast Li+intercalation kinetics into a graphite anode from the electrolyte as well as analysing progress in the commercialization of fast-charging LIBs.展开更多
Magnesium potassium phosphate cement(MKPC)coatings exhibit potential for carbon steel protection but face challenges in practical application due to the preparation process and properties.This study develops flake gra...Magnesium potassium phosphate cement(MKPC)coatings exhibit potential for carbon steel protection but face challenges in practical application due to the preparation process and properties.This study develops flake graphite(FG)-modified MKPC coatings via spraying process,investigating the effects of FG size and dosage on phase composition,microstructure,mechanical properties,corrosion protection,and thermal conductivity.Results show that a low FG dosage(5 wt%)synergistically optimizes multifunctional performance.Compared to unmodified MKPC,FG2-1 exhibited exceptional impact resistance,associated with a 57%reduction in corrosion current density(icorr),a 356.3% increase in low-frequency impedance modulus(Z_(0.01 Hz))and a 37% increase in thermal conductivity.However,the coating with a high FG dosage(15 wt%)degraded performance due to defect accumulation and reduced crystallinity of KMgPO_(4)·6H_(2)O.This work advances the rational design of multifunctional inorganic coatings for extreme service environments requiring coupled corrosion protection and thermal management.展开更多
High-performance graphite materials have important roles in aerospace and nuclear reactor technologies because of their outstanding chemical stability and high-temperature performance.Their traditional production meth...High-performance graphite materials have important roles in aerospace and nuclear reactor technologies because of their outstanding chemical stability and high-temperature performance.Their traditional production method relies on repeated impregnation-carbonization and graphitization,and is plagued by lengthy preparation cycles and high energy consumption.Phase transition-assisted self-pressurized selfsintering technology can rapidly produce high-strength graphite materials,but the fracture strain of the graphite materials produced is poor.To solve this problem,this study used a two-step sintering method to uniformly introduce micro-nano pores into natural graphite-based bulk graphite,achieving improved fracture strain of the samples without reducing their density and mechanical properties.Using natural graphite powder,micron-diamond,and nano-diamond as raw materials,and by precisely controlling the staged pressure release process,the degree of diamond phase transition expansion was effectively regulated.The strain-to-failure of the graphite samples reached 1.2%,a 35%increase compared to samples produced by fullpressure sintering.Meanwhile,their flexural strength exceeded 110 MPa,and their density was over 1.9 g/cm^(3).The process therefore produced both a high strength and a high fracture strain.The interface evolution and toughening mechanism during the two-step sintering process were investigated.It is believed that the micro-nano pores formed have two roles:as stress concentrators they induce yielding by shear and as multi-crack propagation paths they significantly lengthen the crack propagation path.The two-step sintering phase transition strategy introduces pores and provides a new approach for increasing the fracture strain of brittle materials.展开更多
CeO_(2) based semiconductor are widely used in solar-driven photothermal catalytic dry reforming of methane(DRM)reaction,but still suffer from low activity and low light utilization efficiency.This study developed gra...CeO_(2) based semiconductor are widely used in solar-driven photothermal catalytic dry reforming of methane(DRM)reaction,but still suffer from low activity and low light utilization efficiency.This study developed graphite-CeO_(2) interfaces to enhance solar-driven photothermal catalytic DRM.Compared with carbon nanotubes-modified CeO_(2)(CeO_(2)-CNT),graphite-modified CeO_(2)(CeO_(2)-GRA)constructed graphite-CeO_(2) interfaces with distortion in CeO_(2),leading to the formation abundant oxygen vacancies.These graphite-CeO_(2) interfaces with oxygen vacancies enhanced optical absorption and promoted the generation and separation of photogenerated carriers.The high endothermic capacity of graphite elevated the catalyst surface temperature from 592.1−691.3℃,boosting light-to-thermal conversion.The synergy between photogenerated carriers and localized heat enabled Ni/CeO_(2)-GRA to achieve a CO production rate of 9985.6 mmol/(g·h)(vs 7192.4 mmol/(g·h)for Ni/CeO_(2))and a light-to-fuel efficiency of 21.8%(vs 13.8%for Ni/CeO_(2)).This work provides insights for designing graphite-semiconductor interfaces to advance photothermal catalytic efficiency.展开更多
Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of t...Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of the graphite used in the fuel element for these reactors being susceptible to molten salt infiltration,carbon black(CB)was added to increase the density of the graphite,and a fuel element(TRISO(tri-structural isotropic)fuel particles were randomly distributed in the modified graphite matrix)was prepared by cold isostatic pressing process.An out-of-pile performance study shows that the densification and pore structure of the modified graphite matrix were improved,as was the resistance to molten salt infiltration.The median pore size of the modified graphite was reduced from 673 to 433 nm and the threshold pressure for molten salt(FLiBe,66%(molar fraction)LiF and 34%BeF_(2))infiltration was increased from 0.88 to 1.37 MPa.The isotropic CB made the graphite matrix less anisotropic,while its thermal conductivity and compressive strength were reduced due to the difficult graphitization of CB.Fuel elements containing 20%(volume fraction)TRISO particles were prepared.Numerical simulations show that the power and temperature distribution of the fuel were in line with the design requirements.The modified graphite matrix had a higher density,smaller pores,a lower anisotropy and a greater resistance to FLiBe infiltration.展开更多
The transverse rupture strength(TRS)is a key mechanical property for brittle Ti(C,N)-based cermets.However,the complicated structure with the ceramics hard phase and the metal binder phase makes it challenging to asce...The transverse rupture strength(TRS)is a key mechanical property for brittle Ti(C,N)-based cermets.However,the complicated structure with the ceramics hard phase and the metal binder phase makes it challenging to ascertain the essential impact on the TRS.To fundamentally understand the fracture in this system,herein,we present a theoretical model to investigate the essential TRS including friction stress at the phase boundary and Peierls stress of dislocations based on the first-principles method,in which the strain-stress method and Peierls-Nabarro method are employed.The traditional application of this method is analyzing the contributions to the yield strength(YS)in the constitution equation.In this article,we present a transformation of the TRS calculation into YS calculation in terms of some basic mechanical theories,thereby extending the applicability of this method to the calculation of TRS.And,the numerical valuations with good linear fit between the experimental TRS and calculated TRS including intrinsic strength,Hall-Petch effect,as well as dislocation density hardening provide solid evidence for the accuracy of our deductions and theoretical model.Finally,it is evident that the brittle components in cermets are not typically the ceramic phase itself.Our methodology illuminates a novel yet effective approach for analyzing fracture in Ti(C,N)-based cermets,which may be extended to other brittle materials in future.展开更多
The stability of matrix graphite under neutron irradiation and in corrosive environments is crucial for the safe operation of molten salt reactors(MSRs).Raman spectroscopy and a slow positron beam were employed to inv...The stability of matrix graphite under neutron irradiation and in corrosive environments is crucial for the safe operation of molten salt reactors(MSRs).Raman spectroscopy and a slow positron beam were employed to investigate the effects of He ion irradiation fluences and subsequent annealing on the microstructure and defects of the matrix graphite.He ions with 500 keV energy and fluences ranging from 1.1×10^(15)ions∕cm^(2)to 3.5×10^(17)ions∕cm^(2)were used to simulate neutron irradiation at 300 K.The samples with an irradiation fluence of 3.5×10^(16)ions∕cm^(2)were subjected to isochronal annealing at different temperatures(573 K,873 K and 1173 K)for 3 h.The Raman results revealed that the D peak gradually increased,whereas the intrinsic G peak decreased with increasing irradiation fluence.At the same irradiation fluence,the D peak gradually decreased,whereas the intrinsic G peak increased with increasing annealing temperature.Slow positron beam analysis demonstrated that the density or size of irradiation defects(vacancy type)increased with higher irradiation fluence,but decreased rapidly with increasing annealing temperature.The Raman spectral analysis of sample cross sections subjected to high irradiation fluences revealed the emergence of amorphization precisely at the depth where ion damage was most pronounced,whereas the surface retained its crystalline structure.Raman and positron annihilation analyses indicated that the matrix graphite exhibited good irradiation resistance to He ions at 300 K.However,vacancy-type defects induced by He ion irradiation exhibit poor thermal stability and can be easily removed during annealing.展开更多
The advancement of planar micro-supercapacitors(PMSCs)for micro-electromechanical systems(MEMS)has been significantly hindered by the challenge of achieving high energy and power densities.This study addresses this is...The advancement of planar micro-supercapacitors(PMSCs)for micro-electromechanical systems(MEMS)has been significantly hindered by the challenge of achieving high energy and power densities.This study addresses this issue by leveraging screen-printing technology to fabricate high-performance PMSCs using innovative composite ink.The ink,a synergistic blend of few-layer graphene(Gt),carbon black(CB),and NiCo_(2)O_(4),was meticulously mixed to form a conductive and robust coating that enhanced the capacitive performance of the PMSCs.The optimized ink formulation and printing process result in a micro-supercapacitor with an exceptional areal capacitance of 18.95 mF/cm^(2)and an areal energy density of 2.63μW·h/cm^(2)at a current density of 0.05 mA/cm^(2),along with an areal power density of 0.025 mW/cm^(2).The devices demonstrated impressive durability with a capacitance retention rate of 94.7%after a stringent 20000-cycle test,demonstrating their potential for long-term applications.Moreover,the PMSCs displayed excellent mechanical flexibility,with a capacitance decrease of only 3.43%after 5000 bending cycles,highlighting their suitability for flexible electronic devices.The ease of integrating these PMSCs into series and parallel configurations for customized power further underscores their practicality for integrated power supply solutions in various technologies.展开更多
The durability performance in molten aluminum with high chemical activity is considered to be a crucial factor for the application of traditional ceramicmatrix composites in the aluminum industry.Herein,novel Ti(C,N)c...The durability performance in molten aluminum with high chemical activity is considered to be a crucial factor for the application of traditional ceramicmatrix composites in the aluminum industry.Herein,novel Ti(C,N)cermet composites with excellent corrosion resistance,featuring distinct ratios of high-entropy alloy binders,were meticulously synthesized by spark plasma sintering(SPS).The synergetic effect of porosity and binder on the corrosion resistance was detailed analyzed.The results show that 8 wt%binder provides an optimum balance of porosity,hardness,fracture toughness and corrosion resistance of the cermets.The appealing corrosion resistance is intimately associated with the formation of a continuous layer consisting of Ti N/Al N,which is introduced through the decarburization of the Ti(C,N)cermets.Additionally,a corrosion mechanism is proposed to elucidate the formation of alternating morphologies within the reaction layers of the cermets.This work is beneficial for selecting structural materials for use in the aluminum industry.展开更多
As an alternative to lithium-ion batteries,aqueous zinc-graphite batteries(ZnGBs)are being explored as safer and low-cost options with the expectation of scalability to large energy storage systems.However,the current...As an alternative to lithium-ion batteries,aqueous zinc-graphite batteries(ZnGBs)are being explored as safer and low-cost options with the expectation of scalability to large energy storage systems.However,the currently adopted polyatomic and metal complex anion intercalation process at the graphite electrode in ZnGB exhibits poor electrochemical performances.Alternatively,incorporating halogen anions offers exceptional electrochemical performance to graphite electrodes due to their redox process.In this work,ZnGBs are assembled using a LiCl/ZnCl2/KBr^(-)based water-in-salt electrolyte,which efficiently supplies bromide(Br^(−))ions for conversion into Br_(x)^(−)and facilitates Br_(2)intercalation at the graphite electrode.The conversion and intercalation of bromine together enable the ZnGB to achieve a discharge capacity of 2.73 mAh/cm^(2)with 91.0%of coulombic efficiency(CE)while supporting high current density operations of up to 150 mA/cm^(2).With high energy density(4.56 Wh/cm^(2)),high power density(199.5 mW/cm^(2)),and excellent rate capability(∼93.0%CE at 150 mA/cm^(2)),the ZnGB is shown to operate efficiently for as much as 800 cycles.Beguilingly,an anode-free ZnGB offers enhanced stability for up to 1100 cycles without performance decay,matching the electrochemical performance of Zn metal electrodes.This work provides insights into the bromine reaction mechanism at graphite electrodes and the role of surface exfoliation in enabling efficient Br_(x)^(−)formation,along with Br_(2)intercalation,for achieving high-performance ZnGBs.展开更多
Mixed polyanion phosphate Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_(7)(NFPP)is regarded as the most promising cathode material for sodium-ion batteries(SIBs),due to its high structural stability and low-cost environmental frien...Mixed polyanion phosphate Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_(7)(NFPP)is regarded as the most promising cathode material for sodium-ion batteries(SIBs),due to its high structural stability and low-cost environmental friendliness.However,its intrinsic low conductivity and sluggish Na^(+)diffusion restricted the fast-charge and low-temperature sodium storage.Herein,an NFPP composite encapsulated by in-situ pyrolytic carbon and coupled with expanded graphite(NFPP@C/EG)was constructed via a sol-gel method followed by a ballmill procedure.Due to the dual-carbon modified strategy,this NFPP@C/EG only enhanced the electronic conductivity,but also endowed more channels for Na^(+)diffusion.As cathode for SIBs,the optimized NFPP(M-NFPP@C/EG)delivers excellent rate capability(capacity of~80.5 mAh/g at 50 C)and outstanding cycling stability(11000 cycles at 50 C with capacity retention of 89.85%).Additionally,cyclic voltammetry(CV)confirmed that its sodium storage behavior is pseudocapacitance-controlled,with in-situ electrochemical impedance spectroscopy(EIS)further elucidating improvements in electrode reaction kinetics.At lower temperatures(0℃),M-NFPP@C/EG demonstrated exceptional cycling performance(8800 cycles at 10 C with capacity retention of 95.81%).Moreover,pouch cells also exhibited excellent stability.This research demonstrates the feasibility of a dual carbon modification strategy in enhancing NFPP and proposes a low-cost,high-rate,and ultra-stable cathode material for SIBs.展开更多
Although graphite(G)materials dominate the commercial lithium-ion battery(LIBs)anode market due to their excellent overall performance,their limited rate performance and cycle life hinder applications in highperforman...Although graphite(G)materials dominate the commercial lithium-ion battery(LIBs)anode market due to their excellent overall performance,their limited rate performance and cycle life hinder applications in highperformance fields.To improve the cycling and rate performance of graphite anodes,this study first employed economical and eco-friendly tannic acid(TA)as a carbon coating precursor to coat graphite surfaces viaπ-πstacking interactions.In an oxygen-rich alkaline environment,tannic acid undergoes oxidation polymerization and crosslinks with formaldehyde to form a polymer matrix that coats the graphite surface.After subsequent carbonization,carbon-coated graphite material(G@C)was successfully synthesized.Carbon coatings on graphite effectively lower LIB resistance,enhance lithium-ion diffusion,and prevent exfoliation during cycling,thereby significantly boosting rate performance and prolonging the cycle life of graphite.After 500 cycles at 2C,the specific capacity of G@C was 103.7 mAh g^(-1),with a retention of 89%.However,G exhibited only 68.7 mAh g^(-1) and 85%retention under identical conditions.This carbon-coated graphite modification strategy offers a novel,green,and economical approach for designing and tailoring graphite anode materials for lithium-ion batteries with long cycle life and high rate.展开更多
基金financially supported by the Nation Natural Science Foundation of China (Grant No.51575368)
文摘Based on the functionally graded materials （FGMs） design concept, the laminated-graded graphite/cermets self-lubricating composite was prepared to achieve the integration of mechanical prop- erties and lubrication performance of the cermet. The effects of the layer number and thickness of graded structure on residual stresses in the gradient composites were investigated by finite element method （FEM）. From the FEM analyses, the optimal gradient structure design was obtained correspond- ing to the following parameters： the number of graded layers n = 2 and the thickness of graded structure t = I ram. According to the optimum design, a graded graphite/cermets self-lubricating material with two layers was fabricated by a typical powder metallurgy technique. Compared with the homogenous graphite/cermets composite, the surface hardness and indentation fracture toughness of graded compos- ite were increased by approximately 15.9% and 6.3%, respectively. The results of X-ray diffraction （XRD） stress measurement identified the existence of residual compressive stress on the surface of graded com- posite. Additionally, the friction and wear tests revealed that the wear resistance of the graphite/cermets self-lubricating composite was improved significantly via the graded structural design, whereas the coefficient of friction changed slightly.
基金supported by European Union's Horizon Europe,UK Research and Innovation(UKRI).
文摘Graphite,encompassing both natural graphite and synthetic graphite,and graphene,have been extensively utilized and investigated as anode materials and additives in lithium-ion batteries(LIBs).In the pursuit of carbon neutrality,LIBs are expected to play a pivotal role in reducing CO_(2)emissions by decreasing reliance on fossil fuels and enabling the integration of renewable energy sources.Owing to their technological maturity and exceptional electrochemical performance,the global production of graphite and graphene for LIBs is projected to continue expanding.Over the past decades,numerous researchers have concentrated on reducing the material and energy input whilst optimising the electrochemical performance of graphite and graphene,through novel synthesis methods and various modifications at the laboratory scale.This review provides a comprehensive examination of the manufacturing methods,environmental impact,research progress,and challenges associated with graphite and graphene in LIBs from an industrial perspective,with a particular focus on the carbon footprint of production processes.Additionally,it considers emerging challenges and future development directions of graphite and graphene,offering significant insights for ongoing and future research in the field of green LIBs.
基金supported by the National Key Research and Development Program of China(2024YFA1612900)the National Natural Science Foundation of China(Grant No.52103365 and No.12375270)the Guangdong Innovative and Entrepreneurial Research Team Program,China(Grant No.2021ZT09L227).
文摘Fine-grained nuclear graphite is a key material in high-temperature gas-cooled reactors(HTGRs).During air ingress accidents,core graphite components undergo severe oxidation,threatening structural integrity.Therefore,understanding the oxidation behavior of nuclear graphite is essential for reactor safety.The influence of oxidation involves multiple factors,including temperature,sample size,oxidant,impurities,filler type and size,etc.The size of the filler particles plays a crucial role in this study.Five ultrafine-and superfine-grained nuclear graphite samples(5.9-34.4μm)are manufactured using identical raw materials and manufacturing processes.Isothermal oxidation tests conducted at 650℃-750℃ are used to study the oxidation behavior.Additionally,comprehensive characterization is performed to analyze the crystal structure,surface morphology,and nanoscale to microscale pore structure of the samples.Results indicate that oxidation behavior cannot be predicted solely based on filler grain size.Reactive site concentration,characterized by active surface area,dominates the chemical reaction kinetics,whereas pore tortuosity,quantified by the structural parameterΨ,plays a key role in regulating oxidant diffusion.These findings clarify the dual role of microstructure in oxidation mechanisms and establish a theoretical and experimental basis for the design of high-performance nuclear graphite capable of long-term service in high-temperature gas-cooled reactors.
基金Project(U19A2099)supported by the National Natural Science Foundation of China。
文摘In order to effectively prevent the contamination of carbon particle volatiles during high-purity SiC crystals are prepared using the physical vapor transport(PVT)method in ultra-high temperature environments(T³2000℃),this study innovatively attempts to protect graphite materials with SiC reinforced pyrolytic graphite(PyG)coating.It is discovered by preparing the SiC particle layer,the degree of graphitization and stability of PyG coating can be improved.The corrosion test results demonstrated that the SiC reinforced PyG coating can maintain an intact coating with a high graphitization degree after the SiC vapour corrosion test of 2050℃-120 h.Conversely,the samples with and without PyG coating reveal porous and eroded surfaces.Furthermore,following the SiC vapour corrosion test,the PyG coating sample’s integral ratio of D-band and G-band(I_(D)/I_(G))of Raman spectrum test data,reduced by 6.5%,while the SiC reinforced PyG coating decreased by 17.2%,indicating its excellent corrosion resistance.The application of SiC reinforced pyrolytic graphite coating in preparing the SiC single crystal might received a theoretical foundation according to this work.
基金supported by the National Research Foundation of Korea(NRF)grant funded by the Korean government(MSIT)(No.NRF-2021M3H4A1A02048529)the Ministry of Trade,Industry and Energy(MOTIE)of the Korean government under grant No.RS-2022-00155854support from the DGIST Supercomputing and Big Data Center.
文摘To enhance the electrochemical performance of lithium-ion battery anodes with higher silicon content,it is essential to engineer their microstructure for better lithium-ion transport and mitigated volume change as well.Herein,we suggest an effective approach to control the micropore structure of silicon oxide(SiO_(x))/artificial graphite(AG)composite electrodes using a perforated current collector.The electrode features a unique pore structure,where alternating high-porosity domains and low-porosity domains markedly reduce overall electrode resistance,leading to a 20%improvement in rate capability at a 5C-rate discharge condition.Using microstructure-resolved modeling and simulations,we demonstrate that the patterned micropore structure enhances lithium-ion transport,mitigating the electrolyte concentration gradient of lithium-ion.Additionally,perforating current collector with a chemical etching process increases the number of hydrogen bonding sites and enlarges the interface with the SiO_(x)/AG composite electrode,significantly improving adhesion strength.This,in turn,suppresses mechanical degradation and leads to a 50%higher capacity retention.Thus,regularly arranged micropore structure enabled by the perforated current collector successfully improves both rate capability and cycle life in SiO_(x)/AG composite electrodes,providing valuable insights into electrode engineering.
基金supported by the National Natural Science Foundation of China(No.52274346).
文摘Waste graphitization cathode carbon blocks are a type of hazardous solid waste generated during the aluminum electrolysis process,and their proper disposal is a key step in the resource utilization of discarded graphite.This study utilizes the porous“defect advantage”of a cathode carbon block matrix to prepare silicon-doped and asphalt-coated detoxified and purified waste graphitization cathode carbon blocks for use as high-performance silicon/carbon composite anode materials.The results show that the uniformly silicondoped silicon/carbon composite material features a unique amorphous carbon-encapsulated“locked silicon”structure,which effectively addresses issues such as cathode volume expansion,excessive growth of the solid electrolyte interphase(SEI)film,and poor electrical contact between active materials.Consequently,electrochemical performance is enhanced.After assembly in a half-cell,the PSCC/10%Si@C(purified waste graphitization cathode carbon/10%Si@C)material exhibits optimal electrochemical stability,with an initial charging specific capacity of 514.5 mAh/g at 0.1 C(1 C=170 mA/g)and a capacity retention rate of 95.1%after 100 cycles.At a charge rate of 2.0 C,a specific capacity of 216.9 mAh/g is achieved.This technology provides a new pathway for the economical and high-value utilization of waste cathode carbon blocks and the development of low-cost,high-performance anode materials.
基金Funded by Scientific and Technological Innovation Project of Carbon Emission Peak and Carbon Neutrality of Jiangsu Province(No.BE2022028-4)。
文摘We adopted the solution impregnation route with aluminum dihydrogen phosphate solution as liquid medium for effective surface modification on graphite substrate.The mass ratio of graphite to Al(H_(2)PO_(4))_(3) changed from 0.5:1 to 4:1,and the impregnation time changed from 1 to 7 h.The typical composite phase change thermal storage materials doped with the as-treated graphite were fabricated using form-stable technique.To investigate the oxidation and anti-oxidation behavior of the impregnated graphite at high temperatures,the samples were put into a muffle furnace for a cyclic heat test.Based on SEM,EDS,DSC techniques,analyses on the impregnated technique suggested an optimized processing conditions of a 3 h impregnation time with the ratio of graphite:Al(H_(2)PO_(4))_(3) as 1:3 for graphite impregnation treatment.Further investigations on high-temperature phase change heat storage materials doped by the treated graphite suggested excellent oxidation resistance and thermal cycling performance.
文摘Lithium-ion batteries(LIBs)are an electrochemical energy storage technology that has been widely used for portable electrical devices,electric vehicles,and grid storage,etc.To satisfy the demand for user convenience especially for electric vehicles,the development of a fast-charging technology for LIBs has become a critical focus.In commercial LIBs,the slow kinetics of Li+intercalation into the graphite anode from the electrolyte solution is known as the main restriction for fast-charging.We summarize the recent advances in obtaining fast-charging graphite-based anodes,mainly involving modifications of the electrolyte solution and graphite anode.Specifically,strategies for increasing the ionic conductivity and regulating the Li+solvation/desolvation state in the electrolyte solution,as well as optimizing the fabrication and the intrinsic activity of graphite-based anodes are discussed in detail.This review considers practical ways to obtain fast Li+intercalation kinetics into a graphite anode from the electrolyte as well as analysing progress in the commercialization of fast-charging LIBs.
基金National Key Research and Development Program of China(2024YFB3714804)National Natural Science Foundation of China(52171277)+1 种基金Baima Lake Laboratory Joint Funds of the Zhejiang Provincial Natural Science Foundation of China(LBMHZ24E020001)Shanxi-Zheda Institute of Advanced Materials and Chemical Engineering(2022SZ-TD006).
文摘Magnesium potassium phosphate cement(MKPC)coatings exhibit potential for carbon steel protection but face challenges in practical application due to the preparation process and properties.This study develops flake graphite(FG)-modified MKPC coatings via spraying process,investigating the effects of FG size and dosage on phase composition,microstructure,mechanical properties,corrosion protection,and thermal conductivity.Results show that a low FG dosage(5 wt%)synergistically optimizes multifunctional performance.Compared to unmodified MKPC,FG2-1 exhibited exceptional impact resistance,associated with a 57%reduction in corrosion current density(icorr),a 356.3% increase in low-frequency impedance modulus(Z_(0.01 Hz))and a 37% increase in thermal conductivity.However,the coating with a high FG dosage(15 wt%)degraded performance due to defect accumulation and reduced crystallinity of KMgPO_(4)·6H_(2)O.This work advances the rational design of multifunctional inorganic coatings for extreme service environments requiring coupled corrosion protection and thermal management.
基金Natural Science Foundation of Shanghai(24ZR1400800)he Natural Science Foundation of China(U23A20685,52073058,91963204)+1 种基金the National Key R&D Program of China(2021YFB3701400)Shanghai Sailing Program(23YF1400200)。
文摘High-performance graphite materials have important roles in aerospace and nuclear reactor technologies because of their outstanding chemical stability and high-temperature performance.Their traditional production method relies on repeated impregnation-carbonization and graphitization,and is plagued by lengthy preparation cycles and high energy consumption.Phase transition-assisted self-pressurized selfsintering technology can rapidly produce high-strength graphite materials,but the fracture strain of the graphite materials produced is poor.To solve this problem,this study used a two-step sintering method to uniformly introduce micro-nano pores into natural graphite-based bulk graphite,achieving improved fracture strain of the samples without reducing their density and mechanical properties.Using natural graphite powder,micron-diamond,and nano-diamond as raw materials,and by precisely controlling the staged pressure release process,the degree of diamond phase transition expansion was effectively regulated.The strain-to-failure of the graphite samples reached 1.2%,a 35%increase compared to samples produced by fullpressure sintering.Meanwhile,their flexural strength exceeded 110 MPa,and their density was over 1.9 g/cm^(3).The process therefore produced both a high strength and a high fracture strain.The interface evolution and toughening mechanism during the two-step sintering process were investigated.It is believed that the micro-nano pores formed have two roles:as stress concentrators they induce yielding by shear and as multi-crack propagation paths they significantly lengthen the crack propagation path.The two-step sintering phase transition strategy introduces pores and provides a new approach for increasing the fracture strain of brittle materials.
文摘CeO_(2) based semiconductor are widely used in solar-driven photothermal catalytic dry reforming of methane(DRM)reaction,but still suffer from low activity and low light utilization efficiency.This study developed graphite-CeO_(2) interfaces to enhance solar-driven photothermal catalytic DRM.Compared with carbon nanotubes-modified CeO_(2)(CeO_(2)-CNT),graphite-modified CeO_(2)(CeO_(2)-GRA)constructed graphite-CeO_(2) interfaces with distortion in CeO_(2),leading to the formation abundant oxygen vacancies.These graphite-CeO_(2) interfaces with oxygen vacancies enhanced optical absorption and promoted the generation and separation of photogenerated carriers.The high endothermic capacity of graphite elevated the catalyst surface temperature from 592.1−691.3℃,boosting light-to-thermal conversion.The synergy between photogenerated carriers and localized heat enabled Ni/CeO_(2)-GRA to achieve a CO production rate of 9985.6 mmol/(g·h)(vs 7192.4 mmol/(g·h)for Ni/CeO_(2))and a light-to-fuel efficiency of 21.8%(vs 13.8%for Ni/CeO_(2)).This work provides insights for designing graphite-semiconductor interfaces to advance photothermal catalytic efficiency.
文摘Based on the service characteristics of fuel elements for molten salt reactors,they need to have a high power density,resistance to coolant infiltration,and excellent thermodynamic properties.To solve the problem of the graphite used in the fuel element for these reactors being susceptible to molten salt infiltration,carbon black(CB)was added to increase the density of the graphite,and a fuel element(TRISO(tri-structural isotropic)fuel particles were randomly distributed in the modified graphite matrix)was prepared by cold isostatic pressing process.An out-of-pile performance study shows that the densification and pore structure of the modified graphite matrix were improved,as was the resistance to molten salt infiltration.The median pore size of the modified graphite was reduced from 673 to 433 nm and the threshold pressure for molten salt(FLiBe,66%(molar fraction)LiF and 34%BeF_(2))infiltration was increased from 0.88 to 1.37 MPa.The isotropic CB made the graphite matrix less anisotropic,while its thermal conductivity and compressive strength were reduced due to the difficult graphitization of CB.Fuel elements containing 20%(volume fraction)TRISO particles were prepared.Numerical simulations show that the power and temperature distribution of the fuel were in line with the design requirements.The modified graphite matrix had a higher density,smaller pores,a lower anisotropy and a greater resistance to FLiBe infiltration.
基金financially supported by the National Key R&D Program of China(no.2022YFB3706600)the Central Fund to Guide Local Scientific and Technological Development,China(no.20231ZDH04044).
文摘The transverse rupture strength(TRS)is a key mechanical property for brittle Ti(C,N)-based cermets.However,the complicated structure with the ceramics hard phase and the metal binder phase makes it challenging to ascertain the essential impact on the TRS.To fundamentally understand the fracture in this system,herein,we present a theoretical model to investigate the essential TRS including friction stress at the phase boundary and Peierls stress of dislocations based on the first-principles method,in which the strain-stress method and Peierls-Nabarro method are employed.The traditional application of this method is analyzing the contributions to the yield strength(YS)in the constitution equation.In this article,we present a transformation of the TRS calculation into YS calculation in terms of some basic mechanical theories,thereby extending the applicability of this method to the calculation of TRS.And,the numerical valuations with good linear fit between the experimental TRS and calculated TRS including intrinsic strength,Hall-Petch effect,as well as dislocation density hardening provide solid evidence for the accuracy of our deductions and theoretical model.Finally,it is evident that the brittle components in cermets are not typically the ceramic phase itself.Our methodology illuminates a novel yet effective approach for analyzing fracture in Ti(C,N)-based cermets,which may be extended to other brittle materials in future.
基金supported by the National Natural Science Foundation of China(Nos.12005289,52072397)State Key Laboratory of Nuclear Detection and Electronics,University of Science and Technology of China(SKLPDE-KF-202316).
文摘The stability of matrix graphite under neutron irradiation and in corrosive environments is crucial for the safe operation of molten salt reactors(MSRs).Raman spectroscopy and a slow positron beam were employed to investigate the effects of He ion irradiation fluences and subsequent annealing on the microstructure and defects of the matrix graphite.He ions with 500 keV energy and fluences ranging from 1.1×10^(15)ions∕cm^(2)to 3.5×10^(17)ions∕cm^(2)were used to simulate neutron irradiation at 300 K.The samples with an irradiation fluence of 3.5×10^(16)ions∕cm^(2)were subjected to isochronal annealing at different temperatures(573 K,873 K and 1173 K)for 3 h.The Raman results revealed that the D peak gradually increased,whereas the intrinsic G peak decreased with increasing irradiation fluence.At the same irradiation fluence,the D peak gradually decreased,whereas the intrinsic G peak increased with increasing annealing temperature.Slow positron beam analysis demonstrated that the density or size of irradiation defects(vacancy type)increased with higher irradiation fluence,but decreased rapidly with increasing annealing temperature.The Raman spectral analysis of sample cross sections subjected to high irradiation fluences revealed the emergence of amorphization precisely at the depth where ion damage was most pronounced,whereas the surface retained its crystalline structure.Raman and positron annihilation analyses indicated that the matrix graphite exhibited good irradiation resistance to He ions at 300 K.However,vacancy-type defects induced by He ion irradiation exhibit poor thermal stability and can be easily removed during annealing.
基金supported by the Shanxi Province Central Guidance Fund for Local Science and Technology Development Project(YDZJSX2024D030)the National Natural Science Foundation of China(22075197,22278290)+2 种基金the Shanxi Province Key Research and Development Program Project(2021020660301013)the Shanxi Provincial Natural Science Foundation of China(202103021224079)the Research and Development Project of Key Core and Common Technology of Shanxi Province(20201102018).
文摘The advancement of planar micro-supercapacitors(PMSCs)for micro-electromechanical systems(MEMS)has been significantly hindered by the challenge of achieving high energy and power densities.This study addresses this issue by leveraging screen-printing technology to fabricate high-performance PMSCs using innovative composite ink.The ink,a synergistic blend of few-layer graphene(Gt),carbon black(CB),and NiCo_(2)O_(4),was meticulously mixed to form a conductive and robust coating that enhanced the capacitive performance of the PMSCs.The optimized ink formulation and printing process result in a micro-supercapacitor with an exceptional areal capacitance of 18.95 mF/cm^(2)and an areal energy density of 2.63μW·h/cm^(2)at a current density of 0.05 mA/cm^(2),along with an areal power density of 0.025 mW/cm^(2).The devices demonstrated impressive durability with a capacitance retention rate of 94.7%after a stringent 20000-cycle test,demonstrating their potential for long-term applications.Moreover,the PMSCs displayed excellent mechanical flexibility,with a capacitance decrease of only 3.43%after 5000 bending cycles,highlighting their suitability for flexible electronic devices.The ease of integrating these PMSCs into series and parallel configurations for customized power further underscores their practicality for integrated power supply solutions in various technologies.
基金financially supported by the National Natural Science Foundation of China(No.52271014)the Foundation of Education Bureau of Hunan Province(No.22B0163)Jiangxi Provincial Department of Education(No.GJJ2200819)。
文摘The durability performance in molten aluminum with high chemical activity is considered to be a crucial factor for the application of traditional ceramicmatrix composites in the aluminum industry.Herein,novel Ti(C,N)cermet composites with excellent corrosion resistance,featuring distinct ratios of high-entropy alloy binders,were meticulously synthesized by spark plasma sintering(SPS).The synergetic effect of porosity and binder on the corrosion resistance was detailed analyzed.The results show that 8 wt%binder provides an optimum balance of porosity,hardness,fracture toughness and corrosion resistance of the cermets.The appealing corrosion resistance is intimately associated with the formation of a continuous layer consisting of Ti N/Al N,which is introduced through the decarburization of the Ti(C,N)cermets.Additionally,a corrosion mechanism is proposed to elucidate the formation of alternating morphologies within the reaction layers of the cermets.This work is beneficial for selecting structural materials for use in the aluminum industry.
基金The authors acknowledge the University of Sharjah for financial support through a competitive research project grant(project number:23020406277)。
文摘As an alternative to lithium-ion batteries,aqueous zinc-graphite batteries(ZnGBs)are being explored as safer and low-cost options with the expectation of scalability to large energy storage systems.However,the currently adopted polyatomic and metal complex anion intercalation process at the graphite electrode in ZnGB exhibits poor electrochemical performances.Alternatively,incorporating halogen anions offers exceptional electrochemical performance to graphite electrodes due to their redox process.In this work,ZnGBs are assembled using a LiCl/ZnCl2/KBr^(-)based water-in-salt electrolyte,which efficiently supplies bromide(Br^(−))ions for conversion into Br_(x)^(−)and facilitates Br_(2)intercalation at the graphite electrode.The conversion and intercalation of bromine together enable the ZnGB to achieve a discharge capacity of 2.73 mAh/cm^(2)with 91.0%of coulombic efficiency(CE)while supporting high current density operations of up to 150 mA/cm^(2).With high energy density(4.56 Wh/cm^(2)),high power density(199.5 mW/cm^(2)),and excellent rate capability(∼93.0%CE at 150 mA/cm^(2)),the ZnGB is shown to operate efficiently for as much as 800 cycles.Beguilingly,an anode-free ZnGB offers enhanced stability for up to 1100 cycles without performance decay,matching the electrochemical performance of Zn metal electrodes.This work provides insights into the bromine reaction mechanism at graphite electrodes and the role of surface exfoliation in enabling efficient Br_(x)^(−)formation,along with Br_(2)intercalation,for achieving high-performance ZnGBs.
基金supported by the National Key Research and Development Program of China(No.2022YFB2502000)the National Natural Science Foundation of China(Nos.U21A20332,51771076,U21A200970,52301266)the Science and Technology Planning Project of Guangzhou(No.2024A04J3332)。
文摘Mixed polyanion phosphate Na_(4)Fe_(3)(PO_(4))_(2)P_(2)O_(7)(NFPP)is regarded as the most promising cathode material for sodium-ion batteries(SIBs),due to its high structural stability and low-cost environmental friendliness.However,its intrinsic low conductivity and sluggish Na^(+)diffusion restricted the fast-charge and low-temperature sodium storage.Herein,an NFPP composite encapsulated by in-situ pyrolytic carbon and coupled with expanded graphite(NFPP@C/EG)was constructed via a sol-gel method followed by a ballmill procedure.Due to the dual-carbon modified strategy,this NFPP@C/EG only enhanced the electronic conductivity,but also endowed more channels for Na^(+)diffusion.As cathode for SIBs,the optimized NFPP(M-NFPP@C/EG)delivers excellent rate capability(capacity of~80.5 mAh/g at 50 C)and outstanding cycling stability(11000 cycles at 50 C with capacity retention of 89.85%).Additionally,cyclic voltammetry(CV)confirmed that its sodium storage behavior is pseudocapacitance-controlled,with in-situ electrochemical impedance spectroscopy(EIS)further elucidating improvements in electrode reaction kinetics.At lower temperatures(0℃),M-NFPP@C/EG demonstrated exceptional cycling performance(8800 cycles at 10 C with capacity retention of 95.81%).Moreover,pouch cells also exhibited excellent stability.This research demonstrates the feasibility of a dual carbon modification strategy in enhancing NFPP and proposes a low-cost,high-rate,and ultra-stable cathode material for SIBs.
基金supported by the Science and Technology Projects of the State Grid Corporation of China(5500-202323102A-1-1-ZN).
文摘Although graphite(G)materials dominate the commercial lithium-ion battery(LIBs)anode market due to their excellent overall performance,their limited rate performance and cycle life hinder applications in highperformance fields.To improve the cycling and rate performance of graphite anodes,this study first employed economical and eco-friendly tannic acid(TA)as a carbon coating precursor to coat graphite surfaces viaπ-πstacking interactions.In an oxygen-rich alkaline environment,tannic acid undergoes oxidation polymerization and crosslinks with formaldehyde to form a polymer matrix that coats the graphite surface.After subsequent carbonization,carbon-coated graphite material(G@C)was successfully synthesized.Carbon coatings on graphite effectively lower LIB resistance,enhance lithium-ion diffusion,and prevent exfoliation during cycling,thereby significantly boosting rate performance and prolonging the cycle life of graphite.After 500 cycles at 2C,the specific capacity of G@C was 103.7 mAh g^(-1),with a retention of 89%.However,G exhibited only 68.7 mAh g^(-1) and 85%retention under identical conditions.This carbon-coated graphite modification strategy offers a novel,green,and economical approach for designing and tailoring graphite anode materials for lithium-ion batteries with long cycle life and high rate.
