As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation ...As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation and fragmentation.This ultimately leads to a decrease in cell capacity.The trends of volume expansion and capacity change of the SiO/graphite(SiO/C)composite electrode during cycling were investigated via in situ expansion monitoring.First,a series of expansion test schemes were designed,and the linear relationship between negative electrode expansion and cell capacity degradation was quantitatively analyzed.Then,the effects of different initial pressures on the long-term cycling performance of the cell were evaluated.Finally,the mechanism of their effects was analyzed by scanning electron microscope.The results show that after 50 cycles,the cell capacity decreases from 2.556 mAh to 1.689 mAh,with a capacity retention ratio(CRR)of only 66.08%.A linear relationship between the capacity retention ratio and thickness expansion was found.Electrochemical measurements and scanning electron microscope images demonstrate that intense stress inhibits the lithiation of the negative electrode and that the electrode is more susceptible to irreversible damage during cycling.Overall,these results reveal the relationship between the cycling performance of SiO and the internal pressure of the electrode from a macroscopic point of view,which provides some reference for the application of SiO/C composite electrodes in lithium-ion batteries.展开更多
The silicon-graphite(Si-C)composite electrode is considered a promising candidate for next-generation commercial electrodes due to its high capacity.However,lithium-ion batteries with silicon electrodes often experien...The silicon-graphite(Si-C)composite electrode is considered a promising candidate for next-generation commercial electrodes due to its high capacity.However,lithium-ion batteries with silicon electrodes often experience capacity fading and poor cyclic performance,primarily due to the mechanical degradation of the solid-electrolyte interphase(SEI).In this work,we present a homogenized constitutive model for Si-C composite electrodes under finite deformation,incorporating lithium-ion concentration-dependent properties.We perform a wrinkling analysis and systematically examine the influence of key parameters,such as modulus and thickness ratios,on the critical conditions for instability.Additionally,we investigate the ratcheting effect across varying silicon contents.Our findings reveal that maintaining the silicon content within an optimal range effectively reduces plastic accumulation during charge–discharge cycles.These insights provide crucial guidance for optimizing the design and fabrication of Si–C electrode systems,enhancing their durability and performance.展开更多
In order to investigate the effect of solid particles dopants on physicochemical properties of α-PbO2 electrodes, a-PbO2 composite electrodes doped with nano-TiO2 and nano-CeO2 particles were respectively prepared on...In order to investigate the effect of solid particles dopants on physicochemical properties of α-PbO2 electrodes, a-PbO2 composite electrodes doped with nano-TiO2 and nano-CeO2 particles were respectively prepared on A1/conductive coating electrodes in 4 mol/L NaOH solution with addition of PbO until saturation by anodic codeposition. The electrodeposition mechanism, morphology, composition and structure of the composite electrodes were characterized by cyclic voltarnmogram （CV）, SEM, EDAX and XRD. Results show that the doping solid particles can not change reaction mechanism of α-PbO2 electrode in alkaline or acid plating bath, but can improve deposition rate and reduce oxygen evolution potential. The doping solid particles can inhibit the growth of a-PbO2 unit cell and improve specific surface area. The diffraction peak intensity of a-PbO2-CeO2-TiO2 composite electrode is lower than that of pure a-PbO2 electrode. The electrocatalytic activity of a-PbO2-2.12%CEO2-3.71%TIO2 composite electrode is the best. The Guglielmi model for CeO2 and TiO2 codeposition with a-PbO2 is also pronosed.展开更多
Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for...Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for DC-SOFCs is a substantial scientific challenge.Herein we investigated the use of La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3)-δ−Ce_(0.8)Gd_(0.2)O_(1.9)(LSCM−GDC)composite electrodes as anodes for La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3)-δelectrolyte-based DC-SOFCs,with Camellia oleifera shell char as the carbon fuel.The LSCM−GDC-anode DC-SOFC delivered a maximum power density of 221 mW/cm^(2) at 800℃ and it significantly improved to 425 mW/cm^(2) after Ni nanoparticles were introduced into the LSCM−GDC anode through wet impregnation.The microstructures of the prepared anodes were characterized,and the stability of the anode in a DC-SOFC and the influence of catalytic activity on open circuit voltage were studied.The above results indicate that LSCM–GDC anode is promising to be applied in DC-SOFCs.展开更多
Composite electrodes prepared by cation exchange resins and activated carbon(AC)were used to adsorb Ⅴ(Ⅳ)in capacitive deionization(CDI).The electrode made of middle resin size(D860/AC M)had the largest specific surf...Composite electrodes prepared by cation exchange resins and activated carbon(AC)were used to adsorb Ⅴ(Ⅳ)in capacitive deionization(CDI).The electrode made of middle resin size(D860/AC M)had the largest specific surface area and mesoporous content than two other composite electrodes.Electrochemical analysis showed that D860/AC M presents higher specific capacitance and electrical double layer capacitor than the others,and significantly lower internal diffusion impedance.Thus,D860/AC M exhibits the highest adsorption capacity and rate of Ⅴ(Ⅳ)among three electrodes.The intra-particle diffusion model fits well in the initial adsorption stage,while the liquid film diffusion model is more suitable for fitting at the later stage.The pseudo-second-order kinetic model is suited for the entire adsorption process.The adsorption of Ⅴ(Ⅳ)on the composite electrode follows that of the Freundlich isotherm.Thermodynamic analysis indicates that the adsorption of Ⅴ(Ⅳ)is an exothermic process with entropy reduction,and the electric field force plays a dominant role in the CDI process.This work aims to improve our understanding of the ion adsorption behaviors and mechanisms on the composite electrodes in CDI.展开更多
The variation of the effective modulus of silicon composite electrodes,which is a fundamental feature to analyze the coupled mechanical–electrochemical behavior of Si-based electrodes in high-capacity lithium-ion bat...The variation of the effective modulus of silicon composite electrodes,which is a fundamental feature to analyze the coupled mechanical–electrochemical behavior of Si-based electrodes in high-capacity lithium-ion batteries,remains qualitatively controversial.To clarify the contradictory experimental results,numerical modeling of a representative volume element with silicon particles,carbon-binder domains(CBDs),and pores has been performed for the lithiation process.The key parameters for modulus variation were identified and evaluated.A mesostructure change is proposed to be a crucial mechanism that affects the modulus variation,and silicon softening is another key mechanism.Silicon softening and the decreasing CBD volume fraction collectively result in a decrease in the effective modulus of the composite,whereas an increase in the silicon volume fraction along with a decrease in porosity has the opposite effect.The findings of this work provide an in-depth and fundamental understanding of the mechanical properties of silicon composite electrodes.展开更多
The super volume changes and severe mechanical degradation have been a hindrance in the wide application of silicon based composite electrodes in commercial lithium-ion batteries(LIBs).Calendering,one procedure in pro...The super volume changes and severe mechanical degradation have been a hindrance in the wide application of silicon based composite electrodes in commercial lithium-ion batteries(LIBs).Calendering,one procedure in producing LIBs'electrodes,is indispensable to ensure low porosity and energy density.However,the repercussions of the calendering process on the physical characteristics related to the behavior of silicon(Si)based electrodes during the electrochemical reaction have not been well understood.Thus,on account of the deformation characteristic of cantilever electrodes,an in-situ technique is employed to analyze the repercussions of calendering status on the coupled electro-chemo-mechanical performances.During the electrochemical cycling,Young's modulus and diffusion-induced stress in composite electrodes are quantified.The results show that the swelling strain,the stress and the modulus of the Si-based electrode and the calendering degree are positively correlated.Meanwhile,the stress induced by diffusion in the active layer tends to increase in the stage of lithiation and reverses during the delithiation process.Accompany with the SEM analysis,we conclude that the calendering process can induce larger stress,driving the formation of cracks in electrodes.These findings can help understand how the calendering process could affect the capacity dissipating and lifetime of Si based electrodes.展开更多
The recently reported silicon/graphite(Si/Gr)composite electrode with a layered structure is a promising approach to achieve high capacity and stable cycling of Si-based electrodes in lithium-ion batteries.However,the...The recently reported silicon/graphite(Si/Gr)composite electrode with a layered structure is a promising approach to achieve high capacity and stable cycling of Si-based electrodes in lithium-ion batteries.However,there is still a need to clarify why particular layered structures are effective and why others are ineffective or even detrimental.In this work,an unreported mechanism dominated by the porosity evolution of electrodes is proposed for the degradation behavior of layered Si/Gr electrodes.First,the effect of layering sequence on the overall electrode performance is investigated experimentally,and the results suggest that the cycling performance of the silicon-on-graphite(SG)electrode is much superior to that of the graphite-on-silicon electrode.To explain this phenomenon,a coupled mechanical-electrochemical porous electrode model is developed,in which the porosity is affected by the silicon expansion and the local constraints.The modeling results suggest that the weaker constraint of the silicon layer in the SG electrode leads to a more insignificant decrease in porosity,and consequently,the more stable cycling performance.The findings of this work provide new insights into the structural design of Si-based electrodes.展开更多
Stretchable organic light-emitting diodes(OLEDs)are important components for flexible/wearable electronics.However,the efficiency of the existing stretchable OLEDs is still much lower as compared with their rigid coun...Stretchable organic light-emitting diodes(OLEDs)are important components for flexible/wearable electronics.However,the efficiency of the existing stretchable OLEDs is still much lower as compared with their rigid counterparts,one of the main reasons being the lack of ideal flexible transparent electrodes.Herein,we propose and develop a printed embedded metal composite electrode(PEMCE)strategy that enables the fabrication of ultra-thin,highly flexible transparent electrodes with robust mechanical properties.With the flexible transparent electrodes serves as the anodes,flexible/stretchable white OLEDs have been successfully constructed,achieving a current efficiency of up to 77.4 cd A^(-1)and a maximum luminance of 34787 cd m^(-2).The current efficiency of the resulting stretchable OLEDs is the highest ever reported for flexible/stretchable white OLEDs,which is about 1.2 times higher than that of the reference rigid devices based on ITO/glass electrodes.The excellent optoelectronic properties of the printed embedded transparent electrodes and the light extraction effect of the Ag-mesh account for the significant increase in current efficiency.Remarkably,the electroluminescence performance still retains~83%of the original luminance even after bending the device 2000 cycles at a radii of~0.5 mm.More importantly,the device can withstand tensile strains of up to~100%,and even mechanical deformation of 90%tensile strain does not result in a significant loss of electroluminescence performance with current efficiency and luminance maintained at over 85%.The results confirm that the PEMCE strategy is effective for constructing ultra-flexible transparent electrodes,showing great promise for use in a variety of flexible/stretchable electronics.展开更多
1 Results The phenomena that affect the membranes could be found in the electrodes when they operate at medium temperature,due to the utilisation of Nafion as an ionomer in the catalytic layer.An approach to improve t...1 Results The phenomena that affect the membranes could be found in the electrodes when they operate at medium temperature,due to the utilisation of Nafion as an ionomer in the catalytic layer.An approach to improve the mechanical properties of the ionomer in the catalytic layer was used: different inorganic compounds (zeolite,titania and zirconia),having different chemical-physical properties,were selected as inorganic fillers due to their water retention capacity and to act as mechanical reinforce by ...展开更多
A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity to...A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity towards VO^(2+)/VO_2^+redox couples in a VRFB was synthesized by a one-step hydrothermal process.The resulting GF-MNO electrodes possess improved electrochemical kinetic reversibility of the vanadium redox reactions compared to pristine GF electrodes,and the corresponding energy efficiency and discharge capacity at 150 m A cm^(-2)are increased by 12.5%and 40%,respectively.The discharge capacity is maintained at 4.8 A h L^(-1)at the ultrahigh current density of 250 m A cm^(-2).Above all,80%of the energy efficiency of the GF-MNO composite electrodes is retained after 120 charge-discharge cycles at 150 m A cm^(-2).Furthermore,these electrodes demonstrated that more evenly distributed catalytic active sites were obtained from the Mn O_2particles under acidic conditions.The proposed synthetic route is facile,and the raw materials are low cost and environmentally friendly.Therefore,these novel GF-MNO electrodes hold great promise in large-scale vanadium redox flow battery energy storage systems.展开更多
Lithium(Li)metal is the most promising electrode for next-gene ration rechargeable batteries.In order to push the commercialization of the lithium metal batteries,a kind of nitrogen(N)-doped composite graphene(NCG)ado...Lithium(Li)metal is the most promising electrode for next-gene ration rechargeable batteries.In order to push the commercialization of the lithium metal batteries,a kind of nitrogen(N)-doped composite graphene(NCG)adopted as the Li plating host was prepared to regulate Li metal nucleation and suppress dendrite growth.Furthermore,a new kind of sandwich-type composite lithium metal(STCL)electrode was developed to improve its application.The STCL electrode can be used as convenient as a piece of Li foil but no dendrite growth.In a symmetric battery,the STCL electrode cycled for more than 4500 h with the overpotential of less than 40 mV.And due to the creative design,the STCL promises the Li-S battery with a prolonged cycling lifespan.展开更多
Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique...Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique. The effects of current density on the chemical composition, electrocatalytic activity, and stability of the composite anode material were investigated by energy dispersive X-ray spectroscopy（EDXS）, anode polarization curves, quasi-stationary polarization（Tafel） curves, electrochemical impedance spectroscopy（EIS）, scanning electron microscopy（SEM）, and X-ray diffraction（XRD）. Results reveal that the composite electrode obtained at 1 A/dm2 possesses the lowest overpotential（0.610 V at 500 A/m2） for oxygen evolution, the best electrocatalytic activity, the longest service life（360 h at 40 °C in 150 g/L H2SO4 solution under 2 A/cm2）, and the lowest cell voltage（2.75 V at 500 A/m2）. Furthermore, with increasing current density, the coating exhibits grain growth and the decrease of content of Mn O2. Only a slight effect on crystalline structure is observed.展开更多
This work describes the electrochemical behaviour of ibuprofen on two types of multi-walled carbon nanotubes based composite electrodes, i.e., multi-walled carbon nanotubes-epoxy （MWCNT） and silver-modified zeolite-...This work describes the electrochemical behaviour of ibuprofen on two types of multi-walled carbon nanotubes based composite electrodes, i.e., multi-walled carbon nanotubes-epoxy （MWCNT） and silver-modified zeolite-multi-wailed carbon nanotubes-epoxy （AgZMWCNT） composites electrodes. The composite electrodes were obtained using two-roll mill procedure. SEM images of surfaces of the composites revealed a homogeneous distribution of the composite components within the epoxy matrix. AgZMWCNT composite electrode exhibited the better electrical conductivity and larger electroactive surface area. The electrochemical determination of ibuprofen （IBP） was achieved using AgZMWCNT by cyclic voltammetry, differential-pulsed voltammetry, square-wave voltammetry and chronoamperometry. The IBP degradation occurred on both composite electrodes under controlled electrolysis at 1.2 and 1.75 V vs. Ag/AgCl, and IBP concentration was determined comparatively by differential-pulsed voltammetry, under optimized conditions using AgZMWCNT electrode and UV-Vis spectrophotometry methods to determine the IBP degradation performance for each electrode. AgZMWCNT electrode exhibited a dual character allowing a double application in IBP degradation process and its control.展开更多
This article proposes a new type of electrode for micro-electro-discharge machining (micro-EDM) , which can produce ultra fine micro components from various kinds of materials including those that cannot be processed ...This article proposes a new type of electrode for micro-electro-discharge machining (micro-EDM) , which can produce ultra fine micro components from various kinds of materials including those that cannot be processed by the silicon or the Litho-graphie Galvanoformung Abformung (LIGA) processings. This electrode is made by way of the electrodeposition process on the basis of the difference between the discharging performance of the electrodeposited coating and that of the matrix to ensure uniform wear of ele...展开更多
Particle based models of composite anodes are useful tools for exploring the behavior of SOFC systems. As part of our efforts to develop models for understanding fuel cells, we have been building models of Ni-YSZ comp...Particle based models of composite anodes are useful tools for exploring the behavior of SOFC systems. As part of our efforts to develop models for understanding fuel cells, we have been building models of Ni-YSZ composite anodes using experimentally measured particle size distributions. The objectives of this study were to characterize the percolation threshold and conductivity of these models in comparison to simpler mono dispersed and biphasic particle size distributions from the literature. We found that the average values for the onset of percolation and the measured conductivity of the models with experimentally measured particle size distributions are similar to those for the simple distributions and the experimentally measured distributions. For all of the configurations evaluated, the onset of percolation in the Nickel phase occurred at a solid fraction of Nickel between 20% and 25%. This corresponded almost exactly to the point at which the coordination number between Nickel phase particles reached 2.2. The significant finding was that the variation in the value for the conductivity, as measured by the standard deviation of the results, was several orders of magnitude higher than for the simpler systems. We explored the validity of our assumptions, specifically the assumption of random particle placement, by building a particle model directly from FIB-SEM data. In this reconstruction, it was clear that the location of particles was not random. Particles of the same type and size had much likelihood of contact higher than would indicated by random location.展开更多
Owing to their very high theoretical capacity, lithium （Li） metal anodes regain widespread attentions for their promising applications for next-generation high-energy-density Li batteries （e.g., lithium-sulfur batt...Owing to their very high theoretical capacity, lithium （Li） metal anodes regain widespread attentions for their promising applications for next-generation high-energy-density Li batteries （e.g., lithium-sulfur batteries, lithium-oxygen batteries, solid-state lithium metal batter- ies）. However, the inherent bottleneck of Li metal anodes, especially the growth of Li dendrites and the related safety concerns, should be well addressed. Owing to their featured micro-/nano-porous structures and intriguing physical properties, nanocarbon materials have been applied as host materials for Li metal anodes. This review summarizes the recent progress in the development of porous nanocarbon materials for safe Li metal anodes. The perspectives regarding the challenges and future development of employing micro-/nano-porous carbon materials in Li metal anodes are also included.展开更多
The synthetic routes of porous carbons and the applications of the functional porous carbon-based composite electrode materials for lithium secondary batteries are reviewed. The synthetic methods have made great break...The synthetic routes of porous carbons and the applications of the functional porous carbon-based composite electrode materials for lithium secondary batteries are reviewed. The synthetic methods have made great breakthroughs to control the pore size and volume, wall thickness, surface area, and connectivity of porous carbons, which result in the development of functional porous carbon-based composite electrode materials. The effects of porous carbons on the electrochemical properties are further discussed. The porous carbons as ideal matrixes to incorporate active materials make a great improvement on the electrochemical properties because of high surface area and pore volume, excellent electronic conductivity, and strong adsorption capacity. Large numbers of the composite electrode materials have been used for the devices of electrochemical energy conversion and storage, such as lithium-ion batteries （LIBs）, Li-S batteries, and Li-O2 batteries. It is believed that functional porous carbon-based composite electrode materials will continuously contribute to the field of lithium secondary batteries.展开更多
Taking the nano-sized carbon black and aniline monomer as precursor and （NH4）2S2O6 as oxidant, the well coated C/polyaniline（C/PANI） composite materials were prepared by in situ polymerization of the aniline on th...Taking the nano-sized carbon black and aniline monomer as precursor and （NH4）2S2O6 as oxidant, the well coated C/polyaniline（C/PANI） composite materials were prepared by in situ polymerization of the aniline on the surface of well-dispersed nano-sized carbon black for supercapacitor. The micro-structure of the C/PANI composite electrode materials were analyzed by SEM. The electrochemical properties of C/ PANI and PANI composite electrode were characterized by means of the galvanostatic charge-discharge experiment, cyclic voltammetric measurement and impedance spectroscopy analysis. The results show that by adding the nano-sized carbon black in the process of chemical polymerization of the aniline, the polyaniline can be in situ polymerized and well-coated onto the carbon black particles, which may effectively improve the aggregation of particles and the electrolyte penetration. What’s more , the maximum of specific capacitance of C/PANI electrode 437.6F·g -1 can be attained. Compared with PANI electrode, C/PANI electrode shows more desired capacitance characteristics, smaller internal resistance and better cycle performance.展开更多
This article reported the electrochemical behaviors of a novel hollow carbon microspheres/manganese dioxide nanosheets(micro-HC/nano-MnO2) composite prepared by an in situ self-limiting deposition method under hydroth...This article reported the electrochemical behaviors of a novel hollow carbon microspheres/manganese dioxide nanosheets(micro-HC/nano-MnO2) composite prepared by an in situ self-limiting deposition method under hydrothermal condition. The results of scanning electron microscopy reveal that MnO2 nanosheets homogeneously grow onto the surface of micro-HC to form a loose-packed microstructure. The quantity of MnO2 required in the electrode layer has thereby been reduced significantly, and higher specific capacitances have been achieved. The micro-HC/nano-MnO2 electrode presents a high capacitance of 239.0 F g-1 at a current density of 5 m A cm-2, which is a strong promise for high-rate electrochemical capacitive energy storage applications.展开更多
基金supported by the Fundamental Research Funds for the Central Universities(WK2090000055)Anhui Provincial Natural Science Foundation of China(2308085QG231).
文摘As a negative electrode material for lithium-ion batteries,silicon monoxide(SiO)suffers from dramatic volume changes during cycling,causing excessive stress within the electrode and resulting in electrode deformation and fragmentation.This ultimately leads to a decrease in cell capacity.The trends of volume expansion and capacity change of the SiO/graphite(SiO/C)composite electrode during cycling were investigated via in situ expansion monitoring.First,a series of expansion test schemes were designed,and the linear relationship between negative electrode expansion and cell capacity degradation was quantitatively analyzed.Then,the effects of different initial pressures on the long-term cycling performance of the cell were evaluated.Finally,the mechanism of their effects was analyzed by scanning electron microscope.The results show that after 50 cycles,the cell capacity decreases from 2.556 mAh to 1.689 mAh,with a capacity retention ratio(CRR)of only 66.08%.A linear relationship between the capacity retention ratio and thickness expansion was found.Electrochemical measurements and scanning electron microscope images demonstrate that intense stress inhibits the lithiation of the negative electrode and that the electrode is more susceptible to irreversible damage during cycling.Overall,these results reveal the relationship between the cycling performance of SiO and the internal pressure of the electrode from a macroscopic point of view,which provides some reference for the application of SiO/C composite electrodes in lithium-ion batteries.
基金supported by the National Natural Science Foundation of China(Grants Nos.12172102 and 12372097)the Fundamental Research Funds for the Central Universities(Grant No.HIT.OCEF.2022013).
文摘The silicon-graphite(Si-C)composite electrode is considered a promising candidate for next-generation commercial electrodes due to its high capacity.However,lithium-ion batteries with silicon electrodes often experience capacity fading and poor cyclic performance,primarily due to the mechanical degradation of the solid-electrolyte interphase(SEI).In this work,we present a homogenized constitutive model for Si-C composite electrodes under finite deformation,incorporating lithium-ion concentration-dependent properties.We perform a wrinkling analysis and systematically examine the influence of key parameters,such as modulus and thickness ratios,on the critical conditions for instability.Additionally,we investigate the ratcheting effect across varying silicon contents.Our findings reveal that maintaining the silicon content within an optimal range effectively reduces plastic accumulation during charge–discharge cycles.These insights provide crucial guidance for optimizing the design and fabrication of Si–C electrode systems,enhancing their durability and performance.
基金Project(51004056) supported by the National Natural Science Foundation of ChinaProject(KKZ6201152009) supported by the Opening Foundation of Key Laboratory of Inorganic Coating Materials,Chinese Academy of Sciences+2 种基金Project(2010ZC052) supported by the Applied Basic Research Foundation of Yunnan Province,ChinaProject(20125314110011) supported by the Specialized Research Fund for the Doctoral Program of Higher EducationProject(2010247) supported by Analysis & Testing Foundation of Kunming University of Science and Technology,China
文摘In order to investigate the effect of solid particles dopants on physicochemical properties of α-PbO2 electrodes, a-PbO2 composite electrodes doped with nano-TiO2 and nano-CeO2 particles were respectively prepared on A1/conductive coating electrodes in 4 mol/L NaOH solution with addition of PbO until saturation by anodic codeposition. The electrodeposition mechanism, morphology, composition and structure of the composite electrodes were characterized by cyclic voltarnmogram （CV）, SEM, EDAX and XRD. Results show that the doping solid particles can not change reaction mechanism of α-PbO2 electrode in alkaline or acid plating bath, but can improve deposition rate and reduce oxygen evolution potential. The doping solid particles can inhibit the growth of a-PbO2 unit cell and improve specific surface area. The diffraction peak intensity of a-PbO2-CeO2-TiO2 composite electrode is lower than that of pure a-PbO2 electrode. The electrocatalytic activity of a-PbO2-2.12%CEO2-3.71%TIO2 composite electrode is the best. The Guglielmi model for CeO2 and TiO2 codeposition with a-PbO2 is also pronosed.
基金Project(2019YFC1907405)supported by the National Key R&D Program of ChinaProject(GJJ200809)supported by the Education Department Project Fund of Jiangxi Province,ChinaProject(2020BAB214021)supported by the Natural Science Foundation of Jiangxi Province,China。
文摘Direct carbon solid oxide fuel cells(DC-SOFCs)are promising,green,and efficient power-generating devices that are fueled by solid carbons and comprise all-solid-state structures.Developing suitable anode materials for DC-SOFCs is a substantial scientific challenge.Herein we investigated the use of La_(0.75)Sr_(0.25)Cr_(0.5)Mn_(0.5)O_(3)-δ−Ce_(0.8)Gd_(0.2)O_(1.9)(LSCM−GDC)composite electrodes as anodes for La_(0.9)Sr_(0.1)Ga_(0.8)Mg_(0.2)O_(3)-δelectrolyte-based DC-SOFCs,with Camellia oleifera shell char as the carbon fuel.The LSCM−GDC-anode DC-SOFC delivered a maximum power density of 221 mW/cm^(2) at 800℃ and it significantly improved to 425 mW/cm^(2) after Ni nanoparticles were introduced into the LSCM−GDC anode through wet impregnation.The microstructures of the prepared anodes were characterized,and the stability of the anode in a DC-SOFC and the influence of catalytic activity on open circuit voltage were studied.The above results indicate that LSCM–GDC anode is promising to be applied in DC-SOFCs.
基金financially supported by the National Natural Science Foundation of China(No.51874222).
文摘Composite electrodes prepared by cation exchange resins and activated carbon(AC)were used to adsorb Ⅴ(Ⅳ)in capacitive deionization(CDI).The electrode made of middle resin size(D860/AC M)had the largest specific surface area and mesoporous content than two other composite electrodes.Electrochemical analysis showed that D860/AC M presents higher specific capacitance and electrical double layer capacitor than the others,and significantly lower internal diffusion impedance.Thus,D860/AC M exhibits the highest adsorption capacity and rate of Ⅴ(Ⅳ)among three electrodes.The intra-particle diffusion model fits well in the initial adsorption stage,while the liquid film diffusion model is more suitable for fitting at the later stage.The pseudo-second-order kinetic model is suited for the entire adsorption process.The adsorption of Ⅴ(Ⅳ)on the composite electrode follows that of the Freundlich isotherm.Thermodynamic analysis indicates that the adsorption of Ⅴ(Ⅳ)is an exothermic process with entropy reduction,and the electric field force plays a dominant role in the CDI process.This work aims to improve our understanding of the ion adsorption behaviors and mechanisms on the composite electrodes in CDI.
基金supported by the National Natural Science Foundation of China (Grant Nos.12072183,11872236 and 12172205)the Key Research Project of Zhejiang Laboratory (No.2021PE0AC02).
文摘The variation of the effective modulus of silicon composite electrodes,which is a fundamental feature to analyze the coupled mechanical–electrochemical behavior of Si-based electrodes in high-capacity lithium-ion batteries,remains qualitatively controversial.To clarify the contradictory experimental results,numerical modeling of a representative volume element with silicon particles,carbon-binder domains(CBDs),and pores has been performed for the lithiation process.The key parameters for modulus variation were identified and evaluated.A mesostructure change is proposed to be a crucial mechanism that affects the modulus variation,and silicon softening is another key mechanism.Silicon softening and the decreasing CBD volume fraction collectively result in a decrease in the effective modulus of the composite,whereas an increase in the silicon volume fraction along with a decrease in porosity has the opposite effect.The findings of this work provide an in-depth and fundamental understanding of the mechanical properties of silicon composite electrodes.
基金supported by the National Natural Science Foundation of China(Grant Nos.12102264).
文摘The super volume changes and severe mechanical degradation have been a hindrance in the wide application of silicon based composite electrodes in commercial lithium-ion batteries(LIBs).Calendering,one procedure in producing LIBs'electrodes,is indispensable to ensure low porosity and energy density.However,the repercussions of the calendering process on the physical characteristics related to the behavior of silicon(Si)based electrodes during the electrochemical reaction have not been well understood.Thus,on account of the deformation characteristic of cantilever electrodes,an in-situ technique is employed to analyze the repercussions of calendering status on the coupled electro-chemo-mechanical performances.During the electrochemical cycling,Young's modulus and diffusion-induced stress in composite electrodes are quantified.The results show that the swelling strain,the stress and the modulus of the Si-based electrode and the calendering degree are positively correlated.Meanwhile,the stress induced by diffusion in the active layer tends to increase in the stage of lithiation and reverses during the delithiation process.Accompany with the SEM analysis,we conclude that the calendering process can induce larger stress,driving the formation of cracks in electrodes.These findings can help understand how the calendering process could affect the capacity dissipating and lifetime of Si based electrodes.
基金supported by the National Natural Science Foundation of China(Grant Nos.12072183,12472174,and 12421002).
文摘The recently reported silicon/graphite(Si/Gr)composite electrode with a layered structure is a promising approach to achieve high capacity and stable cycling of Si-based electrodes in lithium-ion batteries.However,there is still a need to clarify why particular layered structures are effective and why others are ineffective or even detrimental.In this work,an unreported mechanism dominated by the porosity evolution of electrodes is proposed for the degradation behavior of layered Si/Gr electrodes.First,the effect of layering sequence on the overall electrode performance is investigated experimentally,and the results suggest that the cycling performance of the silicon-on-graphite(SG)electrode is much superior to that of the graphite-on-silicon electrode.To explain this phenomenon,a coupled mechanical-electrochemical porous electrode model is developed,in which the porosity is affected by the silicon expansion and the local constraints.The modeling results suggest that the weaker constraint of the silicon layer in the SG electrode leads to a more insignificant decrease in porosity,and consequently,the more stable cycling performance.The findings of this work provide new insights into the structural design of Si-based electrodes.
基金National Natural Science Foundation of China,Grant/Award Numbers:21835003,21422402,21674050,62005126National Key Basic Research Program of China,Grant/Award Numbers:2014CB648300,2017YFB0404501+7 种基金Natural Science Foundation of Jiangsu Province,Grant/Award Numbers:BE2019120,BK20140060Program for Jiangsu Specially-Appointed Professor,Grant/Award Number:RK030STP15001Six Talent Peaks Project of Jiangsu Province,Grant/Award Number:TD-XCL-009333 Project of Jiangsu Province,Grant/Award Number:BRA2017402Leading Talent of Technological Innovation of National Ten-Thousands Talents Program of ChinaExcellent Scientific and Technological Innovative Teams of Jiangsu Higher Education Institutions,Grant/Award Number:TJ217038NUPT Scientific Foundation,Grant/Award Number:NY220152Priority Academic Program Development of Jiangsu Higher Education Institutions(PAPD)。
文摘Stretchable organic light-emitting diodes(OLEDs)are important components for flexible/wearable electronics.However,the efficiency of the existing stretchable OLEDs is still much lower as compared with their rigid counterparts,one of the main reasons being the lack of ideal flexible transparent electrodes.Herein,we propose and develop a printed embedded metal composite electrode(PEMCE)strategy that enables the fabrication of ultra-thin,highly flexible transparent electrodes with robust mechanical properties.With the flexible transparent electrodes serves as the anodes,flexible/stretchable white OLEDs have been successfully constructed,achieving a current efficiency of up to 77.4 cd A^(-1)and a maximum luminance of 34787 cd m^(-2).The current efficiency of the resulting stretchable OLEDs is the highest ever reported for flexible/stretchable white OLEDs,which is about 1.2 times higher than that of the reference rigid devices based on ITO/glass electrodes.The excellent optoelectronic properties of the printed embedded transparent electrodes and the light extraction effect of the Ag-mesh account for the significant increase in current efficiency.Remarkably,the electroluminescence performance still retains~83%of the original luminance even after bending the device 2000 cycles at a radii of~0.5 mm.More importantly,the device can withstand tensile strains of up to~100%,and even mechanical deformation of 90%tensile strain does not result in a significant loss of electroluminescence performance with current efficiency and luminance maintained at over 85%.The results confirm that the PEMCE strategy is effective for constructing ultra-flexible transparent electrodes,showing great promise for use in a variety of flexible/stretchable electronics.
文摘1 Results The phenomena that affect the membranes could be found in the electrodes when they operate at medium temperature,due to the utilisation of Nafion as an ionomer in the catalytic layer.An approach to improve the mechanical properties of the ionomer in the catalytic layer was used: different inorganic compounds (zeolite,titania and zirconia),having different chemical-physical properties,were selected as inorganic fillers due to their water retention capacity and to act as mechanical reinforce by ...
基金supported by the Ministry of Science and Technology of China (2016YFA0202500)the National Natural Science Foundation of China (51772093)the National key Research and Development Program of China (2017YFD0301507)
文摘A mild and simple synthesis process for large-scale vanadium redox flow batteries(VRFBs)energy storage systems is desirable.A graphite felt/Mn O_2(GF-MNO)composite electrode with excellent electrocatalytic activity towards VO^(2+)/VO_2^+redox couples in a VRFB was synthesized by a one-step hydrothermal process.The resulting GF-MNO electrodes possess improved electrochemical kinetic reversibility of the vanadium redox reactions compared to pristine GF electrodes,and the corresponding energy efficiency and discharge capacity at 150 m A cm^(-2)are increased by 12.5%and 40%,respectively.The discharge capacity is maintained at 4.8 A h L^(-1)at the ultrahigh current density of 250 m A cm^(-2).Above all,80%of the energy efficiency of the GF-MNO composite electrodes is retained after 120 charge-discharge cycles at 150 m A cm^(-2).Furthermore,these electrodes demonstrated that more evenly distributed catalytic active sites were obtained from the Mn O_2particles under acidic conditions.The proposed synthetic route is facile,and the raw materials are low cost and environmentally friendly.Therefore,these novel GF-MNO electrodes hold great promise in large-scale vanadium redox flow battery energy storage systems.
基金financially supported by the Beijing Municipal Science and Technology Project(Nos.Z171100000917021 and Z181100004518003)。
文摘Lithium(Li)metal is the most promising electrode for next-gene ration rechargeable batteries.In order to push the commercialization of the lithium metal batteries,a kind of nitrogen(N)-doped composite graphene(NCG)adopted as the Li plating host was prepared to regulate Li metal nucleation and suppress dendrite growth.Furthermore,a new kind of sandwich-type composite lithium metal(STCL)electrode was developed to improve its application.The STCL electrode can be used as convenient as a piece of Li foil but no dendrite growth.In a symmetric battery,the STCL electrode cycled for more than 4500 h with the overpotential of less than 40 mV.And due to the creative design,the STCL promises the Li-S battery with a prolonged cycling lifespan.
基金Projects(51004056,51004057)supported by the National Natural Science Foundation of ChinaProject(KKZ6201152009)supported by the Opening Foundation of Key Laboratory of Inorganic Coating Materials,Chinese Academy of Sciences+2 种基金Project(2010ZC052)supported by the Applied Basic Research Foundation of Yunnan Province,ChinaProject(20125314110011)supported by the Specialized Research Fund for the Doctoral Program of Higher Education,ChinaProject(2010247)supported by Analysis&Testing Foundation of Kunming University of Science and Technology,China
文摘Al/conductive coating/α-Pb O2-Ce O2-Ti O2/β-PbO 2-MnO 2-WC-Zr O2 composite electrode material was prepared on Al/conductive coating/α-PbO 2-Ce O2-Ti O2 substrate by electrochemical oxidation co-deposition technique. The effects of current density on the chemical composition, electrocatalytic activity, and stability of the composite anode material were investigated by energy dispersive X-ray spectroscopy（EDXS）, anode polarization curves, quasi-stationary polarization（Tafel） curves, electrochemical impedance spectroscopy（EIS）, scanning electron microscopy（SEM）, and X-ray diffraction（XRD）. Results reveal that the composite electrode obtained at 1 A/dm2 possesses the lowest overpotential（0.610 V at 500 A/m2） for oxygen evolution, the best electrocatalytic activity, the longest service life（360 h at 40 °C in 150 g/L H2SO4 solution under 2 A/cm2）, and the lowest cell voltage（2.75 V at 500 A/m2）. Furthermore, with increasing current density, the coating exhibits grain growth and the decrease of content of Mn O2. Only a slight effect on crystalline structure is observed.
基金supported by the strategic grant POSDRU/88/1.5/S/50783POSDRU/21/1.5/G/13798+1 种基金POSDRU/89/1.5/S/57649 co-financed by the European Social Fund - Investing in People,within the Sectoral Operational Programme Human Resources Development 2007-2013partially by the PN II-RU-PD129/2010 and PN II Ideas 165/2011
文摘This work describes the electrochemical behaviour of ibuprofen on two types of multi-walled carbon nanotubes based composite electrodes, i.e., multi-walled carbon nanotubes-epoxy （MWCNT） and silver-modified zeolite-multi-wailed carbon nanotubes-epoxy （AgZMWCNT） composites electrodes. The composite electrodes were obtained using two-roll mill procedure. SEM images of surfaces of the composites revealed a homogeneous distribution of the composite components within the epoxy matrix. AgZMWCNT composite electrode exhibited the better electrical conductivity and larger electroactive surface area. The electrochemical determination of ibuprofen （IBP） was achieved using AgZMWCNT by cyclic voltammetry, differential-pulsed voltammetry, square-wave voltammetry and chronoamperometry. The IBP degradation occurred on both composite electrodes under controlled electrolysis at 1.2 and 1.75 V vs. Ag/AgCl, and IBP concentration was determined comparatively by differential-pulsed voltammetry, under optimized conditions using AgZMWCNT electrode and UV-Vis spectrophotometry methods to determine the IBP degradation performance for each electrode. AgZMWCNT electrode exhibited a dual character allowing a double application in IBP degradation process and its control.
基金National Natural Science Foundation of China (50635040)
文摘This article proposes a new type of electrode for micro-electro-discharge machining (micro-EDM) , which can produce ultra fine micro components from various kinds of materials including those that cannot be processed by the silicon or the Litho-graphie Galvanoformung Abformung (LIGA) processings. This electrode is made by way of the electrodeposition process on the basis of the difference between the discharging performance of the electrodeposited coating and that of the matrix to ensure uniform wear of ele...
基金partially supported through a MURI from the United States Office of Naval Research
文摘Particle based models of composite anodes are useful tools for exploring the behavior of SOFC systems. As part of our efforts to develop models for understanding fuel cells, we have been building models of Ni-YSZ composite anodes using experimentally measured particle size distributions. The objectives of this study were to characterize the percolation threshold and conductivity of these models in comparison to simpler mono dispersed and biphasic particle size distributions from the literature. We found that the average values for the onset of percolation and the measured conductivity of the models with experimentally measured particle size distributions are similar to those for the simple distributions and the experimentally measured distributions. For all of the configurations evaluated, the onset of percolation in the Nickel phase occurred at a solid fraction of Nickel between 20% and 25%. This corresponded almost exactly to the point at which the coordination number between Nickel phase particles reached 2.2. The significant finding was that the variation in the value for the conductivity, as measured by the standard deviation of the results, was several orders of magnitude higher than for the simpler systems. We explored the validity of our assumptions, specifically the assumption of random particle placement, by building a particle model directly from FIB-SEM data. In this reconstruction, it was clear that the location of particles was not random. Particles of the same type and size had much likelihood of contact higher than would indicated by random location.
基金financially supported by the National Key Research and Development Program(Nos.2016YFA0202500,2015CB932500)the National Natural Scientific Foundation of China(Nos.21676160,21561130151)
文摘Owing to their very high theoretical capacity, lithium （Li） metal anodes regain widespread attentions for their promising applications for next-generation high-energy-density Li batteries （e.g., lithium-sulfur batteries, lithium-oxygen batteries, solid-state lithium metal batter- ies）. However, the inherent bottleneck of Li metal anodes, especially the growth of Li dendrites and the related safety concerns, should be well addressed. Owing to their featured micro-/nano-porous structures and intriguing physical properties, nanocarbon materials have been applied as host materials for Li metal anodes. This review summarizes the recent progress in the development of porous nanocarbon materials for safe Li metal anodes. The perspectives regarding the challenges and future development of employing micro-/nano-porous carbon materials in Li metal anodes are also included.
基金supported by the Programs of National 973 (2011CB935900)NSFC (51231003 and 21231005)+1 种基金111 Project (B12015)Tianjin High-Tech (10SYSYJC27600)
文摘The synthetic routes of porous carbons and the applications of the functional porous carbon-based composite electrode materials for lithium secondary batteries are reviewed. The synthetic methods have made great breakthroughs to control the pore size and volume, wall thickness, surface area, and connectivity of porous carbons, which result in the development of functional porous carbon-based composite electrode materials. The effects of porous carbons on the electrochemical properties are further discussed. The porous carbons as ideal matrixes to incorporate active materials make a great improvement on the electrochemical properties because of high surface area and pore volume, excellent electronic conductivity, and strong adsorption capacity. Large numbers of the composite electrode materials have been used for the devices of electrochemical energy conversion and storage, such as lithium-ion batteries （LIBs）, Li-S batteries, and Li-O2 batteries. It is believed that functional porous carbon-based composite electrode materials will continuously contribute to the field of lithium secondary batteries.
基金Project(2005CB623703) supported by the National Basic Research Program of China project(5JJ30103) supported bythe Natural Science Foundation of Hunan Province
文摘Taking the nano-sized carbon black and aniline monomer as precursor and （NH4）2S2O6 as oxidant, the well coated C/polyaniline（C/PANI） composite materials were prepared by in situ polymerization of the aniline on the surface of well-dispersed nano-sized carbon black for supercapacitor. The micro-structure of the C/PANI composite electrode materials were analyzed by SEM. The electrochemical properties of C/ PANI and PANI composite electrode were characterized by means of the galvanostatic charge-discharge experiment, cyclic voltammetric measurement and impedance spectroscopy analysis. The results show that by adding the nano-sized carbon black in the process of chemical polymerization of the aniline, the polyaniline can be in situ polymerized and well-coated onto the carbon black particles, which may effectively improve the aggregation of particles and the electrolyte penetration. What’s more , the maximum of specific capacitance of C/PANI electrode 437.6F·g -1 can be attained. Compared with PANI electrode, C/PANI electrode shows more desired capacitance characteristics, smaller internal resistance and better cycle performance.
基金supported by the National Natural Science Foundation of China (51203071, 51363014 and 51362018)China Postdoctoral Science Foundation (2014M552509)+1 种基金the Key Project of Chinese Ministry of Education (212183)the Natural Science Funds for Distinguished Young Scholars of Gansu Province (1111RJDA012)
文摘This article reported the electrochemical behaviors of a novel hollow carbon microspheres/manganese dioxide nanosheets(micro-HC/nano-MnO2) composite prepared by an in situ self-limiting deposition method under hydrothermal condition. The results of scanning electron microscopy reveal that MnO2 nanosheets homogeneously grow onto the surface of micro-HC to form a loose-packed microstructure. The quantity of MnO2 required in the electrode layer has thereby been reduced significantly, and higher specific capacitances have been achieved. The micro-HC/nano-MnO2 electrode presents a high capacitance of 239.0 F g-1 at a current density of 5 m A cm-2, which is a strong promise for high-rate electrochemical capacitive energy storage applications.
