In the development of rechargeable lithium ion batteries(LIBs),silicon anodes have attracted much attention because of their extremely high theoretical capacity,relatively low Li-insertion voltage and the availability...In the development of rechargeable lithium ion batteries(LIBs),silicon anodes have attracted much attention because of their extremely high theoretical capacity,relatively low Li-insertion voltage and the availability of silicon resources.However,their large volume expansion and fragile solid electrolyte interface(SEI)film hinder their commercial application.To solve these problems,Si has been combined with various carbon materials to increase their structural stability and improve their interface properties.The use of different carbon materials,such as amorphous carbon and graphite,as three-dimensional(3D)protective anode coatings that help buffer mechanical strain and isolate the electrolyte is detailed,and novel methods for applying the coatings are outlined.However,carbon materials used as a protective layer still have some disadvantages,necessitating their modification.Recent developments have focused on modifying the protective carbon shells,and substitutes for the carbon have been suggested.展开更多
This work adopts a multi⁃step etching⁃heat treatment strategy to prepare porous silicon microsphere com⁃posite with Sb⁃Sn surface modification and carbon coating(pSi/Sb⁃Sn@C),using industrial grade SiAl alloy micro⁃sp...This work adopts a multi⁃step etching⁃heat treatment strategy to prepare porous silicon microsphere com⁃posite with Sb⁃Sn surface modification and carbon coating(pSi/Sb⁃Sn@C),using industrial grade SiAl alloy micro⁃spheres as a precursor.pSi/Sb⁃Sn@C had a 3D structure with bimetallic(Sb⁃Sn)modified porous silicon micro⁃spheres(pSi/Sb⁃Sn)as the core and carbon coating as the shell.Carbon shells can improve the electronic conductivi⁃ty and mechanical stability of porous silicon microspheres,which is beneficial for obtaining a stable solid electrolyte interface(SEI)film.The 3D porous core promotes the diffusion of lithium ions,increases the intercalation/delithia⁃tion active sites,and buffers the volume expansion during the intercalation process.The introduction of active met⁃als(Sb⁃Sn)can improve the conductivity of the composite and contribute to a certain amount of lithium storage ca⁃pacity.Due to its unique composition and microstructure,pSi/Sb⁃Sn@C showed a reversible capacity of 1247.4 mAh·g^(-1) after 300 charge/discharge cycles at a current density of 1.0 A·g^(-1),demonstrating excellent rate lithium storage performance and enhanced electrochemical cycling stability.展开更多
Cycling and rate performance of natural graphite is still limited by the sluggish kinetics of lithium ions,which can be improved by surface modifications in previous research.Among these methods,amorphous carbon coati...Cycling and rate performance of natural graphite is still limited by the sluggish kinetics of lithium ions,which can be improved by surface modifications in previous research.Among these methods,amorphous carbon coating has been proved to be mature and efficient.However,the significance of coating uniformity in relation to solid electrolyte interphase(SEI)has been largely overlooked.In this study,the uniformity of amorphous carbon coating is adjusted by the particle size of pitch.When discharged-charged at 1 C,graphite half-cells with such uniform coating show 90.3%of the capacity at 0.1 C,while that is 82.1%for non-uniform coating.Additionally,improved initial coulombic efficiency and cycling stability are demonstrated.These can be attributed to graphite anodes featuring a uniform carbon coating that promotes effective and homogeneous LiF formation within the inorganic matrix.This leads to the establishment of a stabilized SEI,confirmed by time-of-flight secondary ion mass spectrometry(TOF-SIMS).This work provides valuable reference into the rational control of graphite interfaces for high electrochemical performance.展开更多
A novel synthesis method of carbon-coated LiNil/3Mnl/3COl/302 cathode material for lithium-ion battery was reported. The carbon coating was produced from a precursor, glucose, by microwave-pyrolysis method. The prepar...A novel synthesis method of carbon-coated LiNil/3Mnl/3COl/302 cathode material for lithium-ion battery was reported. The carbon coating was produced from a precursor, glucose, by microwave-pyrolysis method. The prepared powders were characterized by scanning electron microscopy （SEM）, X-ray diffraction （XRD）, X-ray fluorescence （XRF） and charge/discharge tests. XRD results indicate that the carbon coating does not change the phase structure of LiNil/3Mnl/3C01/302 material. SEM results show that the surface of spherical carbon-coated material becomes rough. Electrochemical performance results show that the carbon coating can improve the cycling performance of LiNii/3Mnl/3C01/302. The specific discharge capacity retention of the carbon-coated LiNi1/3Mnt/3Col/30z reached 85.0%-96.0% at the 50th cycle at 0.2C rate, and the specific discharge capacity retention is improved at a high rate.展开更多
Layered alkali-metal titanate materials are considered as attractive anodes for sodium ion batteries due to their favorable safety and low cost.However,their practical implementation faces major challenges of low elec...Layered alkali-metal titanate materials are considered as attractive anodes for sodium ion batteries due to their favorable safety and low cost.However,their practical implementation faces major challenges of low electronic conductivity and inevitable volume variation during Na^(+)intercalation and de-intercalation,which are generally difficult to conquer by a single modification method.Herein,a synergistic ally enhancing strategy to promote the electrochemical performance of Na_(2)Ti_(2)O_(5)nanowire array anode via simultaneous hydrogenation and carbon coating is developed.Hydrogenation leads to partially reduced titanium;together with conductive carbon layer,it endows Na_(2)Ti_(2)O_(5)with fast electron transport and structural stability.The resulting H-Na_(2)Ti_(2)O_(5)@C anode exhibits enhanced rate capability(8.0C,165 mAh·g^(-1))and stable cycle performance up to 1000 times in sodium-ion half-cells(the capacity of H-Na_(2)Ti_(2)O_(5)without carbon fades drastically after only 100 cycles).In addition,a newcoupling full cell is further designed with graphene hybridized high-voltage Na_(3)(VO_(0.5))_(2)(PO4)_(2)F_(2)as cathode,capable of delivering a high specific energy density of 212.1 Wh·kg^(-1)(based on the mass of both anode and cathode)and good rate and cycling stability.This work may offer inspiration for synergistic optimization of electrode materials for advanced electrochemical energy storage devices.展开更多
The tribology behaviors of Ti6Al7Nb,its alloy with N-ion implantation,and its alloy with diamond-like carbon(DLC)coating were investigated in artificial saliva.Fretting wear tests of untreated,N-ion implanted and DLC ...The tribology behaviors of Ti6Al7Nb,its alloy with N-ion implantation,and its alloy with diamond-like carbon(DLC)coating were investigated in artificial saliva.Fretting wear tests of untreated,N-ion implanted and DLC coated Ti6Al7Nb alloys plate against a Si3N4ball were carried out on a reciprocating sliding fretting wear test rig.Based on the analysis of X-ray diffraction,Raman spectroscopy,3-D profiler,SEM morphologies and frictional kinetics behavior analysis,the damage behavior of surface modification layer was discussed in detail.The results indicated that the fretting wear behavior of Ti6Al7Nb alloy with N-ion implantation was increased with the dose increase of the implanted nitrogen ions.Moreover,the DLC-coated Ti6Al7Nb alloy with low ion implantation could improve the fretting wear behavior greatly.In addition,the Ti6Al7Nb with DLC coating had better ncorrosion resistance due to the special compact structure.All results suggested that the Ti6Al7Nb with DLC coating had better wear resistance than that with N-ion implantation in artificial saliva.展开更多
The superlattice La-Y-Ni-based hydrogen storage alloys have high discharge capacity and are easy to prepare.However,there is still a gap in commercial applications because of the severe corrosion of the alloys in elec...The superlattice La-Y-Ni-based hydrogen storage alloys have high discharge capacity and are easy to prepare.However,there is still a gap in commercial applications because of the severe corrosion of the alloys in electrolyte and poor high-rate dischargeability(HRD).Therefore,(LaSmY)(NiMnAl)_(3.5) alloy was prepared by magnetic levitation induction melting,and then the alloy was coated with different contents(0.1 wt%-1.0 wt%) of nano-carbons by low-temperature sintering with sucrose as the carbon source in this work.The results show that the cyclic stability and HRD of the alloy first increase and then decrease with the increase of carbon contents.The kinetic results show that the electrocatalytic activity and conductivity of the alloy electrodes can be enhanced by carbon coating.The electrochemical properties of the alloy are the best when the carbon coating content is 0.3 wt%.Compared with the uncoated alloy,the maximum discharge capacity(C_(max)) improves from 354.5 to 359.0 mAh/g,the capacity retention rate after 300 cycles(S_(300)) enhances from 73.15% to 80.01%,and the HRD_(1200) of the alloy enhances from 74.39% to 74.39%.展开更多
To address the issues of large volume change and low conductivity of silicon(Si)materials,carbon coatings have been widely employed as surface protection agent and conductive medium to encapsulate the Si materials,whi...To address the issues of large volume change and low conductivity of silicon(Si)materials,carbon coatings have been widely employed as surface protection agent and conductive medium to encapsulate the Si materials,which can improve the electrochemical performance of Si-based electrodes.There has been a strong demand to gain a deeper understanding of the impact of efficient carbon coating over the lithiation and delithiation process of Si materials.Here,we report the first observation of the extended two-phase transformation of carbon-coated Si nanoparticles(Si/C)during electrochemical processes.The Si/C nanoparticles were prepared by sintering Si nanoparticles with polyvinylidene chloride precursor.The Si/C electrode underwent a two-phase transition during the first 20 cycles at 0.2 C,but started to engage in solid solution reaction when the ordered compact carbon coating began to crack.Under higher current density conditions,the electrode was also found to be involved in solid solution reaction,which,however,was due to the overwhelming demand of kinetic property rather than the breaking of the carbon coating.In comparison,the Si/C composites prepared with sucrose possessed more disordered and porous carbon structures,and presented solid solution reaction throughout the entire cycling process.展开更多
Earth-abundant magnetite(Fe_(3)O_(4))as cathode materials in aqueous zinc-ion batteries(ZIBs)is limited by its very low capacity and poor cycling.Here,a combined strategy based on carbon coating and electrolyte optimi...Earth-abundant magnetite(Fe_(3)O_(4))as cathode materials in aqueous zinc-ion batteries(ZIBs)is limited by its very low capacity and poor cycling.Here,a combined strategy based on carbon coating and electrolyte optimization is adopted to improve the performance of Fe_(3)O_(4).The Zn-Fe_(3)O_(4)@C batteries display specific capacities of 93 mAh g^(−1) and 81%capacity retention after 200 cycles.Such performance is attributed to the enhanced electrical conductivity and structural stability of Fe_(3)O_(4)@C nanocomposites with suppressed iron dissolution.Experimental analysis reveals that the charge storage is contributed by diffusion-limited redox reactions and surface-controlled pseudocapacitance.A stretchable Zn-Fe_(3)O_(4)@C battery is further fabricated,showing stable performance when it is bent or stretched.Fe_(3)O_(4) is a promising cathode material for cost-effective,safe,sustainable and wearable energy supplies.展开更多
Li_(3)FeF_(6)has been the focus of research of fluorine-based cathode materials for lithium-ion batteries.Because of the low electronic conductivity of Li3 FeF6,the decrease of particle size,by an energyconsuming long...Li_(3)FeF_(6)has been the focus of research of fluorine-based cathode materials for lithium-ion batteries.Because of the low electronic conductivity of Li3 FeF6,the decrease of particle size,by an energyconsuming long-time ball milling process with carbon,is necessary to achieve a high electrochemical performance.The most successful method to enhance electrochemical activity,carbon coating,seemed to be impracticable,so far,for sensitive fluorides like Li3 FeF6.In this work,carbon coating on Li3 FeF6 particles has been successfully achieved for the first time,while avoiding both extended hydrolysis and Fe(Ⅲ)-Fe(Ⅱ)reduction.The heat treatment and atmosphere,yielding the maximal transformation of organic carbon to both graphitised and disordered carbon,has been determined.Carbon coating,with a thickness of approximately 2.5 nm,has been achieved by controlled thermal decomposition of glucose,under air,at 300℃.Raman and X-ray photoelectron spectroscopy(XPS)experiments have proved the existence of carbon and Fe2O3 on the surface of Li3FeF6 nanoparticles.XPS spectroscopy indicates the presence of organic residues from glucose decomposition.Attempts to further reduce the orga nic carbon content results in a decrease of the amorphous carbon coating layer.Optimised carbon-coated Li3 FeF6 nanoparticles deliver 122 mA h g^(-1)(85%of theoretical capacity)significantly higher than that of a noncoated sample(58 mA h g^(-1)).Even more,a significant beneficial effect of carbon coating on both capacity retention and coulombic efficiency is observed.展开更多
Copper nanowires(CuNWs)are promising electrode materials,especially for used in flexible and transparent electrodes,due to their advantages of earth-abundant,low-cost,high conductivity and flexibility.However,the poor...Copper nanowires(CuNWs)are promising electrode materials,especially for used in flexible and transparent electrodes,due to their advantages of earth-abundant,low-cost,high conductivity and flexibility.However,the poor stability of CuNWs against oxidation and chemic-al corrosion seriously hinders their practical applications.Herein,we propose a facile strategy to improve the chemical stability of CuNWs by in situ coating of carbon protective layer on top of them through hydrothermal carbonization method.The influential factors on the growth of carbon film including the concentration of the glucose precursor(carbon source),hydrothermal temperature,and hydrothermal time are sys-tematically studied.By tailoring these factors,carbon layers with thickness of 3-8 nm can be uniformly grown on CuNWs with appropriate glucose concentration around 80 mg·mL−1,hydrothermal temperature of 160-170°C,and hydrothermal time of 1-3 h.The as-prepared carbon-coated CuNWs show excellent resistance against corrosion and oxidation,and are of great potential to use broadly in various optoelectronic devices.展开更多
Carbon-coating is a simple and practical method to improve the electrochemical performance of soft carbon anode for fast-charging lithium-ion battery,e.g.,reducing the loss of active lithium during the formation of th...Carbon-coating is a simple and practical method to improve the electrochemical performance of soft carbon anode for fast-charging lithium-ion battery,e.g.,reducing the loss of active lithium during the formation of the solid electrolyte interface(SEI)film,and thereby improving the initial coulombic efficiency.However,the systematic study of relationships between carbon-coating layer properties and electrochemical performances is still lacking.Therefore,two soft carbon materials with different carbon-coating layers were used as model materials,which were prepared by vapor-phase method and solid-phase method,respectively.SEM,TEM,XRD and Raman were conducted to characterize the structural evolution of the soft carbon in the coating process.CV,GCPL,EIS and GITT were conducted to analyze the electrochemical performance of carbon-coating soft carbon.This work provides a good guidance for the development of fast-charging soft carbon material.展开更多
Pyrolytic carbon(PyC) coatings are deposited on the Nextel-440 fiber fabrics by chemical vapor deposition(CVD).The dielectric properties of the Nextel-440 fiber fabrics with PyC coatings(Nextel-440/PyC) are investigat...Pyrolytic carbon(PyC) coatings are deposited on the Nextel-440 fiber fabrics by chemical vapor deposition(CVD).The dielectric properties of the Nextel-440 fiber fabrics with PyC coatings(Nextel-440/PyC) are investigated in a temperature range from room temperature to 700℃ in X-band. Compared with the permittivity of the original Nextel-440 received,the complex permittivity of the Nextel-440/PyC(the real part εand the imaginary part ε), is significantly improved: εof the Nextel-440/PyC has a positive temperature coefficient, in contrast, εof the Nextel-440/PyC exhibits a negative temperature coefficient. Moreover, the reflection loss in units of d B is calculated. The results indicate that the microwave absorbing properties of the Nextel-440/PyC coatings is enhanced at 700℃ compared with that at lower temperatures.展开更多
A series of silver-doped graphite-like carbon coatings was prepared on the surface of aluminum alloy using the magnetron sputtering method. The spontaneous escape behavior and inhibition mechanism of silver from graph...A series of silver-doped graphite-like carbon coatings was prepared on the surface of aluminum alloy using the magnetron sputtering method. The spontaneous escape behavior and inhibition mechanism of silver from graphite-like carbon coating were studied. The results showed that when the sample prepared with a 0.01-A current on the silver target was placed in an atmospheric environment for 0.5 h, an apparent silver escape phenomenon could be observed. However, the silver escape phenomenon was not observed for samples prepared with a 0.05-A current on the silver target if the sample was retained in a 10^（-1） Pa vacuum environment, even after 48 h. Compared with the sample placed in the atmospheric environment immediately after an ion plating process, the silver escape time lagged for 6 h. Nanometer-thick pure carbon coating coverage could effectively suppress silver escape. When the coating thickness reached700 nm, permanent retention of silver could be achieved in the silver-doped graphite-like carbon coating.As the silver residue content in the graphite-like carbon coating increased from 2.27 at.% to 5.35 at.%, the interfacial contact resistance of the coating decreased from 51mΩcm^2 to 6 mΩcm^2.展开更多
P-doping is an effective way to modulate the electronic structure and improve the Na+diffusion kinetics of TiO_(2), enabling enhanced electrochemical performance. However, it is a challenge to prepare TiO;with a high ...P-doping is an effective way to modulate the electronic structure and improve the Na+diffusion kinetics of TiO_(2), enabling enhanced electrochemical performance. However, it is a challenge to prepare TiO;with a high P-doping concentration starting from TiO_(2)in a crystalline state. In this work, we design a novel two-step route for constructing a carbon-coated anatase P-doping TiO_(2)nanospheres(denote as(PAn TSS)@NC) with high P-doping concentration, by utilizing amorphous TiO;nanospheres with the ultrahigh specific area as P-doping precursor firstly, and followed by carbon coating treatment. Experimental results demonstrate that P is successfully doped into the crystal lattice and carbon layer is well coated on the surface of TiO_(2), with P-doping and carbon-coating contents of ~13.5 wt% and 10.4 wt%, respectively,which results in the enhanced pseudocapacitive behavior as well as favorable Na+and electron transferring kinetics. The(P-AnTSS)@NC sample shows excellent rate and cycle performance, exhibiting specific capacities of 177 and 115 m Ah/g at 0.1 and 1.0 A/g after 150 and 2000 cycles, respectively.展开更多
It is imperative to develop a novel matching of metallic substrate and self-lubricating coating for aircraft spherical plain bearing in a wide range of service conditions.As a new type of superelastic material,60NiTi ...It is imperative to develop a novel matching of metallic substrate and self-lubricating coating for aircraft spherical plain bearing in a wide range of service conditions.As a new type of superelastic material,60NiTi alloy meets the performance requirements of aerospace bearing materials,but exhibits poor tribological performance,especially under the conditions of dry sliding friction.A Hydrogenated Diamond-Like Carbon(H-DLC)coating was deposited on the 60NiTi alloy to improve its tribological performance.The microstructure and mechanical behavior of the 60NiTi alloy and its H-DLC coating were explored.Results show that improvement of friction and wear performance of the H-DLC coating deposited on the 60NiTi substrate is mainly achieved by graphitization at the friction interface and the transfer film produced on the counterpart ball.The increased friction load leads to intensification of graphitization at the friction interface and formation of continuous and compact transfer film on the surface of the counterpart ball.展开更多
Carbon/carbon （C/C） composites were deposited with graphite-like carbon （GLC） coating, and then, Arg-Gly- Asp acid （RGD） peptides were successfully immobilized onto the functionalized GLC coating. GLC coating wa...Carbon/carbon （C/C） composites were deposited with graphite-like carbon （GLC） coating, and then, Arg-Gly- Asp acid （RGD） peptides were successfully immobilized onto the functionalized GLC coating. GLC coating was utilized to prevent carbon particles releasing and create a uniform surface condition for C/C composites. RGD peptides were utilized to improve biocompatibility of GLC coating. Surface chemical characterizations of functionalized GLC coating were detected by contact angle measurement, X-ray photoelectron spectroscopy and Raman spectra. Optical morphology of GLC coatings was observed by confocal laser scanning microscopy. In vitro biological performance was determined using samples seeded with MC3T3-E1 osteoblast-like cells and cultured for 1 week. Surface characterizations and morphological analysis indicated that C/C composites were covered by a dense and uniform GLC coating. Contact angle of GLC coating was reduced to 27.2° when it was functionalized by H202 oxidation at 40 ℃ for 1 h. In vitro cytological test showed that the RGD peptides immobilized GLC coating had a significant improvement in biocompatibility. It was suggested that RGD peptides provided GLC coating with a bioactive surface to improve cell adhesion and proliferation on C/C composites.展开更多
Changes to the microstructure of a hard carbon(HC)and its solid electrolyte interface(SEI)can be effective in improving the electrode kinetics.However,achieving fast charging using a simple and inexpensive strategy wi...Changes to the microstructure of a hard carbon(HC)and its solid electrolyte interface(SEI)can be effective in improving the electrode kinetics.However,achieving fast charging using a simple and inexpensive strategy without sacrificing its initial Coulombic efficiency remains a challenge in sodium ion batteries.A simple liquid-phase coating approach has been used to generate a pitch-derived soft carbon layer on the HC surface,and its effect on the porosity of HC and SEI chemistry has been studied.A variety of structural characterizations show a soft carbon coating can increase the defect and ultra-micropore contents.The increase in ultra-micropore comes from both the soft carbon coatings and the larger pores within the HC that are partially filled by pitch,which provides more Na+storage sites.In-situ FTIR/EIS and ex-situ XPS showed that the soft carbon coating induced the formation of thinner SEI that is richer in NaF from the electrolyte,which stabilized the interface and promoted the charge transfer process.As a result,the anode produced fastcharging(329.8 mAh g^(−1)at 30 mA g^(−1)and 198.6 mAh g^(−1)at 300 mA g^(−1))and had a better cycling performance(a high capacity retention of 81.4%after 100 cycles at 150 mA g^(−1)).This work reveals the critical role of coating layer in changing the pore structure,SEI chemistry and diffusion kinetics of hard carbon,which enables rational design of sodium-ion battery anode with enhanced fast charging capability.展开更多
Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes i...Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes it attractive as an anode of Li-ion batteries.Herein,through a one-pot facile high-temperature annealing route,using SBA15 as the silicon source,and embedding tin dioxide SnO_(2)particles into carbon coated SiO_(x),the mesoporous SiO_(x)-SnO_(2)@C rod composite was prepared and tested as the anode material.The results revealed that the SnO_(2)particles were distributed uniformly in the wall,which could further improve their volume energy densities.The coated carbon plays a role in maintaining structural integrality during lithiation,and the rich mesopores structure can release the expanded volume and enhance Li-ion transfer.At 0.1 A·g^(-1),the gravimetric and volumetric capacities of the composite were as high as 1271 mAh·g^(-1)and 1573 mAh·cm^(-3),respectively.After 200 cycles,the 95%capacity could be retained compared with that upon the 2nd cycle at 0.5 A·g^(-1).And the rod morphology was well kept,except that the diameter of the rod was 3 times larger than its original size after the cell was discharged into 0.01 V.展开更多
Solid-state batteries(SSBs)with high-capacity Si anodes have been regarded as one of the most promising candidates to meet the large scale energy storage and electrical vehicles due to its intrinsic safety and potenti...Solid-state batteries(SSBs)with high-capacity Si anodes have been regarded as one of the most promising candidates to meet the large scale energy storage and electrical vehicles due to its intrinsic safety and potential high energy density.However,Si suffers from poor electrical conductivity and huge volume change and particles fracture during lithiaiotn and delithiation,which induces low practical energy density.In addition,the SSBs are often operated at high temperature due to the poor physical contact and huge resistance between Si and solid-state electrolyte(SSE).To improve the bulk electronic/ionic conductivity of Si and its interfacial compatibility with SSE,herein,a binder free and self-supporting Si/C film was developed.The monolithic carbon not only enhance the electric conductivity but also release huge stress during lithiation and delithiation.In addition,paired with the flexible and soft poly(vinylidene fluoride)-co-hexafluoropropylene(PVDF-HFP)and Li_(1.3)A_(l0.3)Ti_(1.7)(PO_(4))_(3)(LATP)solid-state electrolyte,a LiF-rich and electrochemical stable solid-electrolyte interphase(SEI)layer is in-situ engineered.The fast bulk and interfacial ionic transportation as well as the mechanical integrity of MSi enable high performance SSBs at room temperature.As a result,high specific capacity of 2137 m Ah/g with an initial Coulombic efficiency of 83.2%is obtained at a rate of 0.5 A/g.Even at a high rate of 3 A/g,the specific capacity is1793 m Ah/g.At a rate of 1 A/g,the Si/C anode delivers a long cycling performance over 500 cycles while maintains a capacity of 1135 mAh/g.This work provides a new strategy that combines charge transfer kinetics and interfacial chemistry design toward high energy density Si-based SSBs.展开更多
文摘In the development of rechargeable lithium ion batteries(LIBs),silicon anodes have attracted much attention because of their extremely high theoretical capacity,relatively low Li-insertion voltage and the availability of silicon resources.However,their large volume expansion and fragile solid electrolyte interface(SEI)film hinder their commercial application.To solve these problems,Si has been combined with various carbon materials to increase their structural stability and improve their interface properties.The use of different carbon materials,such as amorphous carbon and graphite,as three-dimensional(3D)protective anode coatings that help buffer mechanical strain and isolate the electrolyte is detailed,and novel methods for applying the coatings are outlined.However,carbon materials used as a protective layer still have some disadvantages,necessitating their modification.Recent developments have focused on modifying the protective carbon shells,and substitutes for the carbon have been suggested.
文摘This work adopts a multi⁃step etching⁃heat treatment strategy to prepare porous silicon microsphere com⁃posite with Sb⁃Sn surface modification and carbon coating(pSi/Sb⁃Sn@C),using industrial grade SiAl alloy micro⁃spheres as a precursor.pSi/Sb⁃Sn@C had a 3D structure with bimetallic(Sb⁃Sn)modified porous silicon micro⁃spheres(pSi/Sb⁃Sn)as the core and carbon coating as the shell.Carbon shells can improve the electronic conductivi⁃ty and mechanical stability of porous silicon microspheres,which is beneficial for obtaining a stable solid electrolyte interface(SEI)film.The 3D porous core promotes the diffusion of lithium ions,increases the intercalation/delithia⁃tion active sites,and buffers the volume expansion during the intercalation process.The introduction of active met⁃als(Sb⁃Sn)can improve the conductivity of the composite and contribute to a certain amount of lithium storage ca⁃pacity.Due to its unique composition and microstructure,pSi/Sb⁃Sn@C showed a reversible capacity of 1247.4 mAh·g^(-1) after 300 charge/discharge cycles at a current density of 1.0 A·g^(-1),demonstrating excellent rate lithium storage performance and enhanced electrochemical cycling stability.
基金Project(52377220)supported by the National Natural Science Foundation of ChinaProject(kq2208265)supported by the Natural Science Foundation of Changsha,Hunan Province,ChinaProject supported by State Key Laboratory of Powder Metallurgy(Central South University,Changsha,China)。
文摘Cycling and rate performance of natural graphite is still limited by the sluggish kinetics of lithium ions,which can be improved by surface modifications in previous research.Among these methods,amorphous carbon coating has been proved to be mature and efficient.However,the significance of coating uniformity in relation to solid electrolyte interphase(SEI)has been largely overlooked.In this study,the uniformity of amorphous carbon coating is adjusted by the particle size of pitch.When discharged-charged at 1 C,graphite half-cells with such uniform coating show 90.3%of the capacity at 0.1 C,while that is 82.1%for non-uniform coating.Additionally,improved initial coulombic efficiency and cycling stability are demonstrated.These can be attributed to graphite anodes featuring a uniform carbon coating that promotes effective and homogeneous LiF formation within the inorganic matrix.This leads to the establishment of a stabilized SEI,confirmed by time-of-flight secondary ion mass spectrometry(TOF-SIMS).This work provides valuable reference into the rational control of graphite interfaces for high electrochemical performance.
基金Project(U1202272)supported by the National Natural Science Foundation of China
文摘A novel synthesis method of carbon-coated LiNil/3Mnl/3COl/302 cathode material for lithium-ion battery was reported. The carbon coating was produced from a precursor, glucose, by microwave-pyrolysis method. The prepared powders were characterized by scanning electron microscopy （SEM）, X-ray diffraction （XRD）, X-ray fluorescence （XRF） and charge/discharge tests. XRD results indicate that the carbon coating does not change the phase structure of LiNil/3Mnl/3C01/302 material. SEM results show that the surface of spherical carbon-coated material becomes rough. Electrochemical performance results show that the carbon coating can improve the cycling performance of LiNii/3Mnl/3C01/302. The specific discharge capacity retention of the carbon-coated LiNi1/3Mnt/3Col/30z reached 85.0%-96.0% at the 50th cycle at 0.2C rate, and the specific discharge capacity retention is improved at a high rate.
基金financially supported by the National Natural Science Foundation of China(Nos.52072136,51872104,51972257 and 52172229)the National Key R&D Program of China(No.2016YFA0202602)the Fundamental Research Funds for the Central Universities(No.WUT:2021IVA115)
文摘Layered alkali-metal titanate materials are considered as attractive anodes for sodium ion batteries due to their favorable safety and low cost.However,their practical implementation faces major challenges of low electronic conductivity and inevitable volume variation during Na^(+)intercalation and de-intercalation,which are generally difficult to conquer by a single modification method.Herein,a synergistic ally enhancing strategy to promote the electrochemical performance of Na_(2)Ti_(2)O_(5)nanowire array anode via simultaneous hydrogenation and carbon coating is developed.Hydrogenation leads to partially reduced titanium;together with conductive carbon layer,it endows Na_(2)Ti_(2)O_(5)with fast electron transport and structural stability.The resulting H-Na_(2)Ti_(2)O_(5)@C anode exhibits enhanced rate capability(8.0C,165 mAh·g^(-1))and stable cycle performance up to 1000 times in sodium-ion half-cells(the capacity of H-Na_(2)Ti_(2)O_(5)without carbon fades drastically after only 100 cycles).In addition,a newcoupling full cell is further designed with graphene hybridized high-voltage Na_(3)(VO_(0.5))_(2)(PO4)_(2)F_(2)as cathode,capable of delivering a high specific energy density of 212.1 Wh·kg^(-1)(based on the mass of both anode and cathode)and good rate and cycling stability.This work may offer inspiration for synergistic optimization of electrode materials for advanced electrochemical energy storage devices.
文摘The tribology behaviors of Ti6Al7Nb,its alloy with N-ion implantation,and its alloy with diamond-like carbon(DLC)coating were investigated in artificial saliva.Fretting wear tests of untreated,N-ion implanted and DLC coated Ti6Al7Nb alloys plate against a Si3N4ball were carried out on a reciprocating sliding fretting wear test rig.Based on the analysis of X-ray diffraction,Raman spectroscopy,3-D profiler,SEM morphologies and frictional kinetics behavior analysis,the damage behavior of surface modification layer was discussed in detail.The results indicated that the fretting wear behavior of Ti6Al7Nb alloy with N-ion implantation was increased with the dose increase of the implanted nitrogen ions.Moreover,the DLC-coated Ti6Al7Nb alloy with low ion implantation could improve the fretting wear behavior greatly.In addition,the Ti6Al7Nb with DLC coating had better ncorrosion resistance due to the special compact structure.All results suggested that the Ti6Al7Nb with DLC coating had better wear resistance than that with N-ion implantation in artificial saliva.
基金The financial supports provided by the National Key R&D Program of China (2019YFE0103600)。
文摘The superlattice La-Y-Ni-based hydrogen storage alloys have high discharge capacity and are easy to prepare.However,there is still a gap in commercial applications because of the severe corrosion of the alloys in electrolyte and poor high-rate dischargeability(HRD).Therefore,(LaSmY)(NiMnAl)_(3.5) alloy was prepared by magnetic levitation induction melting,and then the alloy was coated with different contents(0.1 wt%-1.0 wt%) of nano-carbons by low-temperature sintering with sucrose as the carbon source in this work.The results show that the cyclic stability and HRD of the alloy first increase and then decrease with the increase of carbon contents.The kinetic results show that the electrocatalytic activity and conductivity of the alloy electrodes can be enhanced by carbon coating.The electrochemical properties of the alloy are the best when the carbon coating content is 0.3 wt%.Compared with the uncoated alloy,the maximum discharge capacity(C_(max)) improves from 354.5 to 359.0 mAh/g,the capacity retention rate after 300 cycles(S_(300)) enhances from 73.15% to 80.01%,and the HRD_(1200) of the alloy enhances from 74.39% to 74.39%.
基金This study is funded by the Assistant Secretary for Energy Efficiency,Vehicle Technologies Office of the U.S.Department of Energy,under the Si Consortium Program.Electron microscopy experiments are conducted at the National Centre for Electron Microscopy and the Molecular Foundry located at Lawrence Berkeley National Laboratory is supported by the Director,Office of Science,Office of Basic Energy Sciences,the U.S.Department of Energy under Contract No.DE-AC02-05CH11231.
文摘To address the issues of large volume change and low conductivity of silicon(Si)materials,carbon coatings have been widely employed as surface protection agent and conductive medium to encapsulate the Si materials,which can improve the electrochemical performance of Si-based electrodes.There has been a strong demand to gain a deeper understanding of the impact of efficient carbon coating over the lithiation and delithiation process of Si materials.Here,we report the first observation of the extended two-phase transformation of carbon-coated Si nanoparticles(Si/C)during electrochemical processes.The Si/C nanoparticles were prepared by sintering Si nanoparticles with polyvinylidene chloride precursor.The Si/C electrode underwent a two-phase transition during the first 20 cycles at 0.2 C,but started to engage in solid solution reaction when the ordered compact carbon coating began to crack.Under higher current density conditions,the electrode was also found to be involved in solid solution reaction,which,however,was due to the overwhelming demand of kinetic property rather than the breaking of the carbon coating.In comparison,the Si/C composites prepared with sucrose possessed more disordered and porous carbon structures,and presented solid solution reaction throughout the entire cycling process.
基金This work was supported by National Natural Science Foundation of China(51873088)the Tianjin Municipal Science and Technology Commission(18JCZDJC38400)in China.
文摘Earth-abundant magnetite(Fe_(3)O_(4))as cathode materials in aqueous zinc-ion batteries(ZIBs)is limited by its very low capacity and poor cycling.Here,a combined strategy based on carbon coating and electrolyte optimization is adopted to improve the performance of Fe_(3)O_(4).The Zn-Fe_(3)O_(4)@C batteries display specific capacities of 93 mAh g^(−1) and 81%capacity retention after 200 cycles.Such performance is attributed to the enhanced electrical conductivity and structural stability of Fe_(3)O_(4)@C nanocomposites with suppressed iron dissolution.Experimental analysis reveals that the charge storage is contributed by diffusion-limited redox reactions and surface-controlled pseudocapacitance.A stretchable Zn-Fe_(3)O_(4)@C battery is further fabricated,showing stable performance when it is bent or stretched.Fe_(3)O_(4) is a promising cathode material for cost-effective,safe,sustainable and wearable energy supplies.
基金This work was financially supported by the“Agencia Estatal de Investigación/Fondo Europeo de Desarrollo Regional”(FEDER/UE)and“Comunidad de Madrid”(Nos.MAT2016-78632-C4-1-R and S2013/MIT-2753)Characterisation techniques for this research were partially financed by the EU funds(Nos.POPW.01.03.00-20.034/09-00 and POPW.01.03.00-20-004/11-00)。
文摘Li_(3)FeF_(6)has been the focus of research of fluorine-based cathode materials for lithium-ion batteries.Because of the low electronic conductivity of Li3 FeF6,the decrease of particle size,by an energyconsuming long-time ball milling process with carbon,is necessary to achieve a high electrochemical performance.The most successful method to enhance electrochemical activity,carbon coating,seemed to be impracticable,so far,for sensitive fluorides like Li3 FeF6.In this work,carbon coating on Li3 FeF6 particles has been successfully achieved for the first time,while avoiding both extended hydrolysis and Fe(Ⅲ)-Fe(Ⅱ)reduction.The heat treatment and atmosphere,yielding the maximal transformation of organic carbon to both graphitised and disordered carbon,has been determined.Carbon coating,with a thickness of approximately 2.5 nm,has been achieved by controlled thermal decomposition of glucose,under air,at 300℃.Raman and X-ray photoelectron spectroscopy(XPS)experiments have proved the existence of carbon and Fe2O3 on the surface of Li3FeF6 nanoparticles.XPS spectroscopy indicates the presence of organic residues from glucose decomposition.Attempts to further reduce the orga nic carbon content results in a decrease of the amorphous carbon coating layer.Optimised carbon-coated Li3 FeF6 nanoparticles deliver 122 mA h g^(-1)(85%of theoretical capacity)significantly higher than that of a noncoated sample(58 mA h g^(-1)).Even more,a significant beneficial effect of carbon coating on both capacity retention and coulombic efficiency is observed.
基金the National Natural Science Foundation of China(No.21403089)the Fundamental Research Funds for the Central Universities,China(No.2042020kf0195).
文摘Copper nanowires(CuNWs)are promising electrode materials,especially for used in flexible and transparent electrodes,due to their advantages of earth-abundant,low-cost,high conductivity and flexibility.However,the poor stability of CuNWs against oxidation and chemic-al corrosion seriously hinders their practical applications.Herein,we propose a facile strategy to improve the chemical stability of CuNWs by in situ coating of carbon protective layer on top of them through hydrothermal carbonization method.The influential factors on the growth of carbon film including the concentration of the glucose precursor(carbon source),hydrothermal temperature,and hydrothermal time are sys-tematically studied.By tailoring these factors,carbon layers with thickness of 3-8 nm can be uniformly grown on CuNWs with appropriate glucose concentration around 80 mg·mL−1,hydrothermal temperature of 160-170°C,and hydrothermal time of 1-3 h.The as-prepared carbon-coated CuNWs show excellent resistance against corrosion and oxidation,and are of great potential to use broadly in various optoelectronic devices.
基金Science and Technology Program of Zhejiang Province(2022C01071)Major Science and technology projects in Ningbo(2022Z026).
文摘Carbon-coating is a simple and practical method to improve the electrochemical performance of soft carbon anode for fast-charging lithium-ion battery,e.g.,reducing the loss of active lithium during the formation of the solid electrolyte interface(SEI)film,and thereby improving the initial coulombic efficiency.However,the systematic study of relationships between carbon-coating layer properties and electrochemical performances is still lacking.Therefore,two soft carbon materials with different carbon-coating layers were used as model materials,which were prepared by vapor-phase method and solid-phase method,respectively.SEM,TEM,XRD and Raman were conducted to characterize the structural evolution of the soft carbon in the coating process.CV,GCPL,EIS and GITT were conducted to analyze the electrochemical performance of carbon-coating soft carbon.This work provides a good guidance for the development of fast-charging soft carbon material.
基金supported by the National Natural Science Foundation of China(Grant No.51072165)the Fund of the State Key Laboratory of Solidification Processing in Northwestern Polytechnical University,China(Grant Nos.KP201307 and SKLSP201313)
文摘Pyrolytic carbon(PyC) coatings are deposited on the Nextel-440 fiber fabrics by chemical vapor deposition(CVD).The dielectric properties of the Nextel-440 fiber fabrics with PyC coatings(Nextel-440/PyC) are investigated in a temperature range from room temperature to 700℃ in X-band. Compared with the permittivity of the original Nextel-440 received,the complex permittivity of the Nextel-440/PyC(the real part εand the imaginary part ε), is significantly improved: εof the Nextel-440/PyC has a positive temperature coefficient, in contrast, εof the Nextel-440/PyC exhibits a negative temperature coefficient. Moreover, the reflection loss in units of d B is calculated. The results indicate that the microwave absorbing properties of the Nextel-440/PyC coatings is enhanced at 700℃ compared with that at lower temperatures.
基金financial support of the project from the National Natural Science Foundation of China (Nos. 51571114 and 51401106)the Natural Science Foundation of Jiangsu Province (No. BK20130935)
文摘A series of silver-doped graphite-like carbon coatings was prepared on the surface of aluminum alloy using the magnetron sputtering method. The spontaneous escape behavior and inhibition mechanism of silver from graphite-like carbon coating were studied. The results showed that when the sample prepared with a 0.01-A current on the silver target was placed in an atmospheric environment for 0.5 h, an apparent silver escape phenomenon could be observed. However, the silver escape phenomenon was not observed for samples prepared with a 0.05-A current on the silver target if the sample was retained in a 10^（-1） Pa vacuum environment, even after 48 h. Compared with the sample placed in the atmospheric environment immediately after an ion plating process, the silver escape time lagged for 6 h. Nanometer-thick pure carbon coating coverage could effectively suppress silver escape. When the coating thickness reached700 nm, permanent retention of silver could be achieved in the silver-doped graphite-like carbon coating.As the silver residue content in the graphite-like carbon coating increased from 2.27 at.% to 5.35 at.%, the interfacial contact resistance of the coating decreased from 51mΩcm^2 to 6 mΩcm^2.
基金supported by the National Natural Science Foundation of China (No. 21875071)the Guangdong key R&D Program of China (No. 2019B090908001)。
文摘P-doping is an effective way to modulate the electronic structure and improve the Na+diffusion kinetics of TiO_(2), enabling enhanced electrochemical performance. However, it is a challenge to prepare TiO;with a high P-doping concentration starting from TiO_(2)in a crystalline state. In this work, we design a novel two-step route for constructing a carbon-coated anatase P-doping TiO_(2)nanospheres(denote as(PAn TSS)@NC) with high P-doping concentration, by utilizing amorphous TiO;nanospheres with the ultrahigh specific area as P-doping precursor firstly, and followed by carbon coating treatment. Experimental results demonstrate that P is successfully doped into the crystal lattice and carbon layer is well coated on the surface of TiO_(2), with P-doping and carbon-coating contents of ~13.5 wt% and 10.4 wt%, respectively,which results in the enhanced pseudocapacitive behavior as well as favorable Na+and electron transferring kinetics. The(P-AnTSS)@NC sample shows excellent rate and cycle performance, exhibiting specific capacities of 177 and 115 m Ah/g at 0.1 and 1.0 A/g after 150 and 2000 cycles, respectively.
基金co-supported by the National Natural Science Foundation of China(No.51905466)the Aeronautical Science Foundation of China(No.201945099002)+1 种基金the Natural Science Foundation of Hebei Province,China(Nos.E2021203191 and E2020203184)the Youth Top Talent Project of Hebei Province Higher Education,China(No.BJ2019058).
文摘It is imperative to develop a novel matching of metallic substrate and self-lubricating coating for aircraft spherical plain bearing in a wide range of service conditions.As a new type of superelastic material,60NiTi alloy meets the performance requirements of aerospace bearing materials,but exhibits poor tribological performance,especially under the conditions of dry sliding friction.A Hydrogenated Diamond-Like Carbon(H-DLC)coating was deposited on the 60NiTi alloy to improve its tribological performance.The microstructure and mechanical behavior of the 60NiTi alloy and its H-DLC coating were explored.Results show that improvement of friction and wear performance of the H-DLC coating deposited on the 60NiTi substrate is mainly achieved by graphitization at the friction interface and the transfer film produced on the counterpart ball.The increased friction load leads to intensification of graphitization at the friction interface and formation of continuous and compact transfer film on the surface of the counterpart ball.
基金supported by the National Natural Science Foundation of China under Grant Nos.51202194 and 51221001the Programme of Introducing Talents of Discipline to Universities(‘‘111’’project of China)under Grant No.B08040
文摘Carbon/carbon （C/C） composites were deposited with graphite-like carbon （GLC） coating, and then, Arg-Gly- Asp acid （RGD） peptides were successfully immobilized onto the functionalized GLC coating. GLC coating was utilized to prevent carbon particles releasing and create a uniform surface condition for C/C composites. RGD peptides were utilized to improve biocompatibility of GLC coating. Surface chemical characterizations of functionalized GLC coating were detected by contact angle measurement, X-ray photoelectron spectroscopy and Raman spectra. Optical morphology of GLC coatings was observed by confocal laser scanning microscopy. In vitro biological performance was determined using samples seeded with MC3T3-E1 osteoblast-like cells and cultured for 1 week. Surface characterizations and morphological analysis indicated that C/C composites were covered by a dense and uniform GLC coating. Contact angle of GLC coating was reduced to 27.2° when it was functionalized by H202 oxidation at 40 ℃ for 1 h. In vitro cytological test showed that the RGD peptides immobilized GLC coating had a significant improvement in biocompatibility. It was suggested that RGD peptides provided GLC coating with a bioactive surface to improve cell adhesion and proliferation on C/C composites.
基金National Key Research and Development Program of China(2022YFE0206300)National Natural Science Foundation of China(U21A2081,22075074,22209047)+2 种基金Guangdong Basic and Applied Basic Research Foundation(2024A1515011620)Hunan Provincial Natural Science Foundation of China(2024JJ5068)Foundation of Yuelushan Center for Industrial Innovation(2023YCII0119)。
文摘Changes to the microstructure of a hard carbon(HC)and its solid electrolyte interface(SEI)can be effective in improving the electrode kinetics.However,achieving fast charging using a simple and inexpensive strategy without sacrificing its initial Coulombic efficiency remains a challenge in sodium ion batteries.A simple liquid-phase coating approach has been used to generate a pitch-derived soft carbon layer on the HC surface,and its effect on the porosity of HC and SEI chemistry has been studied.A variety of structural characterizations show a soft carbon coating can increase the defect and ultra-micropore contents.The increase in ultra-micropore comes from both the soft carbon coatings and the larger pores within the HC that are partially filled by pitch,which provides more Na+storage sites.In-situ FTIR/EIS and ex-situ XPS showed that the soft carbon coating induced the formation of thinner SEI that is richer in NaF from the electrolyte,which stabilized the interface and promoted the charge transfer process.As a result,the anode produced fastcharging(329.8 mAh g^(−1)at 30 mA g^(−1)and 198.6 mAh g^(−1)at 300 mA g^(−1))and had a better cycling performance(a high capacity retention of 81.4%after 100 cycles at 150 mA g^(−1)).This work reveals the critical role of coating layer in changing the pore structure,SEI chemistry and diffusion kinetics of hard carbon,which enables rational design of sodium-ion battery anode with enhanced fast charging capability.
文摘Due to the high capacity and moderate volume expansion of silicon protoxide SiO_(x)(160%)compared with that of Si(300%),reducing silicon dioxide SiO_(2)into SiO_(x)while maintaining its special nano-morphology makes it attractive as an anode of Li-ion batteries.Herein,through a one-pot facile high-temperature annealing route,using SBA15 as the silicon source,and embedding tin dioxide SnO_(2)particles into carbon coated SiO_(x),the mesoporous SiO_(x)-SnO_(2)@C rod composite was prepared and tested as the anode material.The results revealed that the SnO_(2)particles were distributed uniformly in the wall,which could further improve their volume energy densities.The coated carbon plays a role in maintaining structural integrality during lithiation,and the rich mesopores structure can release the expanded volume and enhance Li-ion transfer.At 0.1 A·g^(-1),the gravimetric and volumetric capacities of the composite were as high as 1271 mAh·g^(-1)and 1573 mAh·cm^(-3),respectively.After 200 cycles,the 95%capacity could be retained compared with that upon the 2nd cycle at 0.5 A·g^(-1).And the rod morphology was well kept,except that the diameter of the rod was 3 times larger than its original size after the cell was discharged into 0.01 V.
基金financially supported by the Natural Science Foundation of Fujian Province(No.2021J01333)the funding from the Fujian Education Department of China(No.JAT210582)。
文摘Solid-state batteries(SSBs)with high-capacity Si anodes have been regarded as one of the most promising candidates to meet the large scale energy storage and electrical vehicles due to its intrinsic safety and potential high energy density.However,Si suffers from poor electrical conductivity and huge volume change and particles fracture during lithiaiotn and delithiation,which induces low practical energy density.In addition,the SSBs are often operated at high temperature due to the poor physical contact and huge resistance between Si and solid-state electrolyte(SSE).To improve the bulk electronic/ionic conductivity of Si and its interfacial compatibility with SSE,herein,a binder free and self-supporting Si/C film was developed.The monolithic carbon not only enhance the electric conductivity but also release huge stress during lithiation and delithiation.In addition,paired with the flexible and soft poly(vinylidene fluoride)-co-hexafluoropropylene(PVDF-HFP)and Li_(1.3)A_(l0.3)Ti_(1.7)(PO_(4))_(3)(LATP)solid-state electrolyte,a LiF-rich and electrochemical stable solid-electrolyte interphase(SEI)layer is in-situ engineered.The fast bulk and interfacial ionic transportation as well as the mechanical integrity of MSi enable high performance SSBs at room temperature.As a result,high specific capacity of 2137 m Ah/g with an initial Coulombic efficiency of 83.2%is obtained at a rate of 0.5 A/g.Even at a high rate of 3 A/g,the specific capacity is1793 m Ah/g.At a rate of 1 A/g,the Si/C anode delivers a long cycling performance over 500 cycles while maintains a capacity of 1135 mAh/g.This work provides a new strategy that combines charge transfer kinetics and interfacial chemistry design toward high energy density Si-based SSBs.
