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Sample records for battery electrodes

  1. Composite electrodes for lithium batteries.

    Energy Technology Data Exchange (ETDEWEB)

    Hackney, S. A.; Johnson, C. S.; Kahaian, A. J.; Kepler, K. D.; Shao-Horn, Y.; Thackeray, M. M.; Vaughey, J. T.

    1999-02-03

    The stability of composite positive and negative electrodes for rechargeable lithium batteries is discussed. Positive electrodes with spinel-type structures that are derived from orthorhombic-LiMnO{sub 2} and layered-MnO{sub 2} are significantly more stable than standard spinel Li[Mn{sub 2}]O{sub 4} electrodes when cycled electrochemically over both the 4-V and 3-V plateaus in lithium cells. Transmission electron microscope data of cycled electrodes have indicated that a composite domain structure accounts for this greater electrochemical stability. The performance of composite Cu{sub x}Sn materials as alternative negative electrodes to amorphous SnO{sub x} electrodes for lithium-ion batteries is discussed in terms of the importance of the concentration of the electrochemically inactive copper component in the electrode.

  2. Negative electrodes for Na-ion batteries.

    Science.gov (United States)

    Dahbi, Mouad; Yabuuchi, Naoaki; Kubota, Kei; Tokiwa, Kazuyasu; Komaba, Shinichi

    2014-08-07

    Research interest in Na-ion batteries has increased rapidly because of the environmental friendliness of sodium compared to lithium. Throughout this Perspective paper, we report and review recent scientific advances in the field of negative electrode materials used for Na-ion batteries. This paper sheds light on negative electrode materials for Na-ion batteries: carbonaceous materials, oxides/phosphates (as sodium insertion materials), sodium alloy/compounds and so on. These electrode materials have different reaction mechanisms for electrochemical sodiation/desodiation processes. Moreover, not only sodiation-active materials but also binders, current collectors, electrolytes and electrode/electrolyte interphase and its stabilization are essential for long cycle life Na-ion batteries. This paper also addresses the prospect of Na-ion batteries as low-cost and long-life batteries with relatively high-energy density as their potential competitive edge over the commercialized Li-ion batteries.

  3. Electrode materials for rechargeable battery

    Energy Technology Data Exchange (ETDEWEB)

    Johnson, Christopher; Kang, Sun-Ho

    2015-09-08

    A positive electrode is disclosed for a non-aqueous electrolyte lithium rechargeable cell or battery. The electrode comprises a lithium containing material of the formula Na.sub.yLi.sub.xNi.sub.zMn.sub.1-z-z'M.sub.z'O.sub.d, wherein M is a metal cation, x+y>1, 0electrode material can be synthesized using an ion-exchange reaction with a lithium salt in an organic-based solvent to partially replace sodium ions of a precursor material with lithium ions.

  4. Long life lithium batteries with stabilized electrodes

    Science.gov (United States)

    Amine, Khalil; Liu, Jun; Vissers, Donald R.; Lu, Wenquan

    2009-03-24

    The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In some embodiments the additives include a substituted or unsubstituted cyclic or spirocyclic hydrocarbon containing at least one oxygen atom and at least one alkenyl or alkynyl group. When used in electrochemical devices with, e.g., lithium manganese oxide spinel electrodes or olivine or carbon-coated olivine electrodes, the new electrolytes provide batteries with improved calendar and cycle life.

  5. Electrode structures and surfaces for Li batteries

    Energy Technology Data Exchange (ETDEWEB)

    Thackeray, Michael M.; Kang, Sun-Ho; Balasubramanian, Mahalingam; Croy, Jason

    2017-03-14

    This invention relates to methods of preparing positive electrode materials for electrochemical cells and batteries. It relates, in particular, to a method for fabricating lithium-metal-oxide electrode materials for lithium cells and batteries. The method comprises contacting a hydrogen-lithium-manganese-oxide material with one or more metal ions, preferably in an acidic solution, to insert the one or more metal ions into the hydrogen-lithium-manganese-oxide material; heat-treating the resulting product to form a powdered metal oxide composition; and forming an electrode from the powdered metal oxide composition.

  6. Nanowire Electrodes for Advanced Lithium Batteries

    Directory of Open Access Journals (Sweden)

    Lei eHuang

    2014-10-01

    Full Text Available Since the commercialization of lithium ion batteries (LIBs in the past two decades, rechargeable LIBs have become widespread power sources for portable devices used in daily life. However, current demands require higher energy density and power density of batteries. The electrochemical energy storage performance of LIBs could be improved by applying nanomaterial electrodes, but their fast capacity fading is still one of the key limitations and the mechanism needs to be clearly understood. Single nanowire electrode devices are considered as a versatile platform for in situ probing the direct relationship between electrical transport, structure change, and other properties of the single nanowire electrode along with the charge/discharge process. The results indicate the conductivity decrease of the nanowire electrode and the structural disorder/destruction during electrochemical reactions which limit the cycling performance of LIBs. Based on the in situ observations, some feasible structure architecture strategies, including prelithiation, coaxial structure, nanowire arrays and hierarchical structure architecture, are proposed and utilized to restrain the conductivity decrease and structural disorder/destruction. Further, the applications of nanowire electrodes in some beyond Li-ion batteries, such as Li-S and Li-air battery, are also described.

  7. Nickel electrode for alkaline batteries

    Energy Technology Data Exchange (ETDEWEB)

    Charkey, A.; Januszkiewicz, S.

    1985-10-08

    A nickel electrode including a conductive support and a layer on the support including a mixture of a nickel active material and a graphite diluent containing a spinel type oxide, the spinel type oxide having the formula M/sub 2/Co/sub 2/O/sub 4/, where M/sub 2/ is Co, Ni, Mn, Fe, Cu, Zn or Cd, or combinations thereof, and having a weight which is in the range of 1-30 percent of the weight of the diluent.

  8. Improved zinc electrode and rechargeable zinc-air battery

    Science.gov (United States)

    Ross, P.N. Jr.

    1988-06-21

    The invention comprises an improved rechargeable zinc-air cell/battery having recirculating alkaline electrolyte and a zinc electrode comprising a porous foam support material which carries the active zinc electrode material. 5 figs.

  9. Graphene-based battery electrodes having continuous flow paths

    Science.gov (United States)

    Zhang, Jiguang; Xiao, Jie; Liu, Jun; Xu, Wu; Li, Xiaolin; Wang, Deyu

    2014-05-24

    Some batteries can exhibit greatly improved performance by utilizing electrodes having randomly arranged graphene nanosheets forming a network of channels defining continuous flow paths through the electrode. The network of channels can provide a diffusion pathway for the liquid electrolyte and/or for reactant gases. Metal-air batteries can benefit from such electrodes. In particular Li-air batteries show extremely high capacities, wherein the network of channels allow oxygen to diffuse through the electrode and mesopores in the electrode can store discharge products.

  10. Phase Transformation Dynamics in Porous Battery Electrodes

    CERN Document Server

    Ferguson, Todd R

    2014-01-01

    Porous electrodes composed of multiphase active materials are widely used in Li-ion batteries, but their dynamics are poorly understood. Two-phase models are largely empirical, and no models exist for three or more phases. Using a modified porous electrode theory based on non-equilibrium thermodynamics, we show that experimental phase behavior can be accurately predicted from free energy models, without artificially placing phase boundaries or fitting the open circuit voltage. First, we simulate lithium intercalation in porous iron phosphate, a popular two-phase cathode, and show that the zero-current voltage gap, sloping voltage plateau and under-estimated exchange currents all result from size-dependent nucleation and mosaic instability. Next, we simulate porous graphite, the standard anode with three stable phases, and reproduce experimentally observed fronts of color-changing phase transformations. These results provide a framework for physics-based design and control for electrochemical systems with comp...

  11. Long life lithium batteries with stabilized electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Amine, Khalil; Liu, Jun; Vissers, Donald R; Lu, Wenquan

    2015-04-21

    The present invention relates to non-aqueous electrolytes having electrode stabilizing additives, stabilized electrodes, and electrochemical devices containing the same. Thus the present invention provides electrolytes containing an alkali metal salt, a polar aprotic solvent, and an electrode stabilizing additive. In certain electrolytes, the alkali metal salt is a bis(chelato)borate and the additives include substituted or unsubstituted linear, branched or cyclic hydrocarbons comprising at least one oxygen atom and at least one aryl, alkenyl or alkynyl group. In other electrolytes, the additives include a substituted aryl compound or a substituted or unsubstituted heteroaryl compound wherein the additive comprises at least one oxygen atom. There are also provided methods of making the electrolytes and batteries employing the electrolytes. The invention also provides for electrode materials. Cathodes of the present invention may be further stabilized by surface coating the particles of the spinel or olivine with a material that can neutralize acid or otherwise lessen or prevent leaching of the manganese or iron ions. In some embodiments the coating is polymeric and in other embodiments the coating is a metal oxide such as ZrO.sub.2, TiO.sub.2, ZnO, WO.sub.3, Al.sub.2O.sub.3, MgO, SiO.sub.2, SnO.sub.2 AlPO.sub.4, Al(OH).sub.3, a mixture of any two or more thereof.

  12. Electrode pattern design for GaAs betavoltaic batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen Haiyang; Yin Jianhua; Li Darang, E-mail: haiyangchen@bit.edu.cn [School of Mechanical Engineering, Beijing Institute of Technology, Beijing 100081 (China)

    2011-08-15

    The sensitivities of betavoltaic batteries and photovoltaic batteries to series and parallel resistance are studied. Based on the study, an electrode pattern design principle of GaAs betavoltaic batteries is proposed. GaAs PIN junctions with and without the proposed electrode pattern are fabricated and measured under the illumination of {sup 63}Ni. Results show that the proposed electrode can reduce the backscattering and shadowing for the beta particles from {sup 63}Ni to increase the GaAs betavoltaic battery short circuit currents effectively but has little impact on the fill factors and ideal factors.

  13. Electrode pattern design for GaAs betavoltaic batteries

    Institute of Scientific and Technical Information of China (English)

    Chen Haiyang; Yin Jianhua; Li Darang

    2011-01-01

    The sensitivities of betavoltaic batteries and photovoltaic batteries to series and parallel resistance are studied.Based on the study,an electrode pattern design principle ofGaAs betavoltaic batteries is proposed.GaAs PIN junctions with and without the proposed electrode pattern are fabricated and measured under the illumination of 63Ni.Results show that the proposed electrode can reduce the backscattering and shadowing for the beta particles from 63Ni to increase the GaAs betavoltaic battery short circuit currents effectively but has little impact on the fill factors and ideal factors.

  14. Lithium metal oxide electrodes for lithium batteries

    Science.gov (United States)

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kang, Sun-Ho

    2010-06-08

    An uncycled preconditioned electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula xLi.sub.2-yH.sub.yO.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 in which 0lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. The xLi.sub.2-yH.sub.y.xM'O.sub.2.(1-x)Li.sub.1-zH.sub.zMO.sub.2 material is prepared by preconditioning a precursor lithium metal oxide (i.e., xLi.sub.2M'O.sub.3.(1-x)LiMO.sub.2) with a proton-containing medium with a pH<7.0 containing an inorganic acid. Methods of preparing the electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

  15. Coupled diffusion and mechanics in battery electrodes

    Science.gov (United States)

    Eshghinejad, Ahmadreza

    We are living in a world with continuous production and consumption of energy. The energy production in the past decades has started to move away from petrochemical sources toward sustainable sources such as solar, wind and geothermal. Also, the energy consumption is further adapting to the sustainable sources. For instance, in recent years electric vehicles are growing fast that can consume sustainable electric energy stored in their batteries. In this direction, in order to further move toward sustainable energy, materials are becoming increasingly important for storing electric energy. Although, currently the technologies such as Li-ion batteries and solid-oxide fuel cells are commercially available for energy applications, improvements are crucial for the next generation of many other technologies producing or consuming sustainable energies. A critical aspect of the electrochemical activities involved in energy storage technologies such as Li-ion batteries and solid-oxide fuel cells is the diffusion of ions into the electrode materials. This process ultimately governs various functional properties of the batteries such as capacity and charging/discharging rates. The first goal of this dissertation is to develop mathematical tools to analyze the ionic diffusion and investigate its coupling with mechanics in electrodes. For this purpose, a thermodynamics-based modeling framework is developed and numerically solved using two numerical methods to analyze ionic diffusion in heterogeneous and structured electrodes. The next goal of this dissertation is to develop and analyze characterization techniques to probe the electrochemical processes at the nano-scale. To this end, the mathematical models are first employed to model a previously developed Atomic Force Microscopy based technique to probe local electrochemical activities called Electrochemical Strain Microscopy (ESM). This method probes the activities by inducing AC electric field to perturb ionic activities and

  16. A method for making electrodes for lead storage batteries

    Energy Technology Data Exchange (ETDEWEB)

    Ivaki, T.; Kobayasi, K.

    1983-06-04

    Powder, acid resistant thermoplastic resin is applied to a greased electrode of a lead storage battery. The electrode is heated until the resin melts, cooled, producing a film of hardened resin with fine cracks in the absence of pores. The electrode has a long service life with cycling.

  17. Zinc electrode and rechargeable zinc-air battery

    Science.gov (United States)

    Ross, Jr., Philip N.

    1989-01-01

    An improved zinc electrode is disclosed for a rechargeable zinc-air battery comprising an outer frame and a porous foam electrode support within the frame which is treated prior to the deposition of zinc thereon to inhibit the formation of zinc dendrites on the external surface thereof. The outer frame is provided with passageways for circulating an alkaline electrolyte through the treated zinc-coated porous foam. A novel rechargeable zinc-air battery system is also disclosed which utilizes the improved zinc electrode and further includes an alkaline electrolyte within said battery circulating through the passageways in the zinc electrode and an external electrolyte circulation means which has an electrolyte reservoir external to the battery case including filter means to filter solids out of the electrolyte as it circulates to the external reservoir and pump means for recirculating electrolyte from the external reservoir to the zinc electrode.

  18. Understanding the Effects of Electrode Formulation on the Mechanical Strength of Composite Electrodes for Flexible Batteries.

    Science.gov (United States)

    Gaikwad, Abhinav M; Arias, Ana Claudia

    2017-02-22

    Flexible lithium-ion batteries are necessary for powering the next generation of wearable electronic devices. In most designs, the mechanical flexibility of the battery is improved by reducing the thickness of the active layers, which in turn reduces the areal capacity and energy density of the battery. The performance of a battery depends on the electrode composition, and in most flexible batteries, standard electrode formulation is used, which is not suitable for flexing. Even with considerable efforts made toward the development of flexible lithium-ion batteries, the formulation of the electrodes has received very little attention. In this study, we investigate the relation between the electrode formulation and the mechanical strength of the electrodes. Peel and drag tests are used to compare the adhesion and cohesion strength of the electrodes. The strength of an electrode is sensitive to the particle size and the choice of polymeric binder. By optimizing the electrode composition, we were able to fabricate a high areal capacity (∼2 mAh/cm(2)) flexible lithium-ion battery with conventional metal-based current collectors that shows superior electrochemical and mechanical performance in comparison to that of batteries with standard composition.

  19. AC impedance study of degradation of porous nickel battery electrodes

    Science.gov (United States)

    Lenhart, Stephen J.; Macdonald, D. D.; Pound, B. G.

    1987-01-01

    AC impedance spectra of porous nickel battery electrodes were recorded periodically during charge/discharge cycling in concentrated KOH solution at various temperatures. A transmission line model (TLM) was adopted to represent the impedance of the porous electrodes, and various model parameters were adjusted in a curve fitting routine to reproduce the experimental impedances. Degradation processes were deduced from changes in model parameters with electrode cycling time. In developing the TLM, impedance spectra of planar (nonporous) electrodes were used to represent the pore wall and backing plate interfacial impedances. These data were measured over a range of potentials and temperatures, and an equivalent circuit model was adopted to represent the planar electrode data. Cyclic voltammetry was used to study the characteristics of the oxygen evolution reaction on planar nickel electrodes during charging, since oxygen evolution can affect battery electrode charging efficiency and ultimately electrode cycle life if the overpotential for oxygen evolution is sufficiently low.

  20. Electrode assembly for a lithium ion battery, process for the production of such electrode assembly, and lithium ion battery comprising such electrode assemblies

    NARCIS (Netherlands)

    Mulder, F.M.; Wagemaker, M.

    2013-01-01

    The invention provides an electrode assembly for a lithium ion battery, the electrode assembly comprising a lithium storage electrode layer on a current collector, wherein the lithium storage electrode layer is a porous layer having a porosity in the range of -35 %, with pores having pore widths in

  1. A method for connecting electrodes in a storage battery

    Energy Technology Data Exchange (ETDEWEB)

    Toda, K.; Karasava, S.

    1983-07-14

    The electrode units, placed into the body of a storage battery (AB), are electrically connected by welding connecting elements which pass through the partitions in the body. The processing is conducted with heating and pressure simultaneously.

  2. Porous graphite electrodes for rechargeable ion-transfer batteries

    Energy Technology Data Exchange (ETDEWEB)

    Novak, P.; Scheifele, W.; Haas, O. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1997-06-01

    The influence of preparation pressure and pore-forming additives on the properties of graphite-based, Li{sup +}-intercalating electrodes for ion-transfer batteries have been investigated. The electrochemical performance of graphite electrodes could be improved by adjusting the porosity. Specific charge of >300 Ah/kg (with respect to the graphite mass) could be achieved. (author) 4 figs., 2 refs.

  3. Graphene Sandwiched Mesostructured Li-Ion Battery Electrodes.

    Science.gov (United States)

    Liu, Jinyun; Zheng, Qiye; Goodman, Matthew D; Zhu, Haoyue; Kim, Jinwoo; Krueger, Neil A; Ning, Hailong; Huang, Xingjiu; Liu, Jinhuai; Terrones, Mauricio; Braun, Paul V

    2016-09-01

    A deterministic graphene-sandwiched Li-ion battery electrode consisting of an integrated 3D mesostructure of electrochemically active materials and graphene is presented. As demonstrations, electrodes with active nanomaterials that coat (V2 O5 @graphene@V2 O5 cathode) or are coated by (graphene@Si@graphene anode) graphene are fabricated. These electrodes exhibit high capacities and ultralong cycle lives (the cathode can be cycled over 2000 times with minimal capacity fade).

  4. Preparation and Electrode Performance of Ferrihydrites For Rechargeable Lithium Batteries

    Institute of Scientific and Technical Information of China (English)

    WANG Hong; LAI Xiao-yong; XIA Wei; YU Ran-bo; MAO Dan; XING Chao-jian; YAO Jian-xi; WANG Dan; LI Xiao-tian

    2008-01-01

    @@ Now LiCoO2 is the most widely used electrode material in commercial rechargeable lithium-based batteries; however, the toxicity of cobalt and the scarcity of cobalt sources, as well as the limited charge/discharge capacity(130-140 mA·h·g-1) of LiCoO2 electrode drive many efforts to develop various alternative electrode materials, including diverse transition metal oxides and their lithiated counterparts[1-3].

  5. Electrode Materials for Lithium/Sodium-Ion Batteries

    DEFF Research Database (Denmark)

    Shen, Yanbin

    2014-01-01

    Shen systematically investigated the controlled synthesis of electrode materials for lithium/sodium ion batteries. She also investigated their formation mechanisms and structural evolution during the operation of batteries using in situ/operando X-ray diffraction techniques. The research findings...... provide insights into formation mechanisms of Li4Ti5O12 anode material from both hydrothermal and solid-state reaction. The results also contribute to a thorough understanding of the intercalation and decay mechanisms of O3/P2 layered sodium cathode materials in sodium ion batteries.......The synthesis of electrode materials for lithium/sodium ion batteries and their structural stability during lithium/sodium insertion/extraction are the two essential issues that have limited battery application in the fields requiring long cycle life and high safety. During her PhD studies, Yanbin...

  6. Recovery Of Electrodic Powder From Spent Lithium Ion Batteries (LIBs

    Directory of Open Access Journals (Sweden)

    Shin S.M.

    2015-06-01

    Full Text Available This study was focused on recycling process newly proposed to recover electrodic powder enriched in cobalt (Co and lithium (Li from spent lithium ion battery. In addition, this new process was designed to prevent explosion of batteries during thermal treatment under inert atmosphere. Spent lithium ion batteries (LIBs were heated over the range of 300°C to 600°C for 2 hours and each component was completely separated inside reactor after experiment. Electrodic powder was successfully recovered from bulk components containing several pieces of metals through sieving operation. The electrodic powder obtained was examined by X-ray diffraction (XRD, energy dispersive X-ray spectroscopy (EDS, and atomic absorption spectroscopy (AA and furthermore image of the powder was taken by scanning electron microscopy (SEM. It was finally found that cobalt and lithium were mainly recovered to about 49 wt.% and 4 wt.% in electrodic powder, respectively.

  7. Coated magnetic particles in electrochemical systems: Synthesis, modified electrodes, alkaline batteries, and paste electrodes

    Science.gov (United States)

    Unlu, Murat

    Magnetic field effects on electrochemical reactions have been studied and shown to influence kinetics and dynamics. Recently, our group has introduced a novel method to establish magnetic field effects by incorporating inert, magnetic microparticles onto the electrode structure. This modification improved several electrochemical systems including modified electrodes, alkaline batteries, and fuel cells. This dissertation describes the applicability of magnetic microparticles and the understanding of magnetic field effects in modified electrodes, alkaline batteries, and paste electrodes. Magnetic effects are studied on electrodes that are coated with an ion exchange polymer that embeds chemically inert, commercial, magnetic microparticles. The flux (electrolysis current) of redox probe to the magnetically modified system is compared to a similar non-magnetic electrode. Flux enhancements of 60% are achieved at magnetically modified electrode as compared to non-magnetic controls. In addition to modifying electrode surfaces, the incorporation of magnetic microparticles into the electrode material itself establishes a 20% increase in flux. Possible magnetic field effects are evaluated. Study of samarium cobalt modified electrolytic manganese dioxide, EMD electrodes further establish a magnetic effect on alkaline cathode performance. Magnetic modification improves alkaline battery performance in primary and secondary applications. The reaction mechanism is examined through voltammetric methods. This work also includes coating protocols to produce inert magnetic microparticles with high magnetic content. Magnetite powders are encapsulated in a polymer matrix by dispersion polymerization. Composite particles are examined in proton exchange membrane fuel cells to study carbon monoxide tolerance.

  8. Stabilization of insertion electrodes for lithium batteries.

    Energy Technology Data Exchange (ETDEWEB)

    Thackeray, M. M.

    1998-09-03

    This paper discusses the techniques that are being employed to stabilize LiMn{sub 2}O{sub 4} spinel and composite Li{sub x}MnO{sub 2} positive electrodes. The critical role that spinel domains play in stabilizing these electrodes for operation at both 4 V and 3 V is highlighted. The concept of using an intermetallic electrode MM{prime} where M is an active alloying element and M{prime} is an inactive element (or elements) is proposed as an alternative negative electrode (to carbon) for lithium-ion cells. An analogy to metal oxide insertion electrodes, such as MnO{sub 2}, in which Mn is the electrochemically active ion and O is the inactive ion, is made. Performance data are given for the copper-tin electrode system, which includes the intermetallic phases eta-Cu{sub 6}Sn{sub 5} and Li{sub 2}CuSn.

  9. Vertically Aligned Carbon Nanotube Electrodes for Lithium-Ion Batteries

    Science.gov (United States)

    2011-01-01

    37] Z. Yang, H. Wu, Mater. Chem. Phys. 71 (2001) 7. [38] D. Linden , T.B. Reddy, Handbook of Batteries , 3rd ed., McGraw-Hill Co., Inc., New York, 2005. ...Lithium-ion Energy storage Battery a b s t r a c t As portable electronics becomemore advanced and alternative energy demands becomemore prevalent, the...aligned carbon nanotube electrodes for lithium-ion batteries 5a. CONTRACT NUMBER 5b. GRANT NUMBER 5c. PROGRAM ELEMENT NUMBER 6. AUTHOR( S ) 5d. PROJECT

  10. Reliable reference electrodes for lithium-ion batteries

    KAUST Repository

    La Mantia, F.

    2013-06-01

    Despite the high attention drawn to the lithium-ion batteries by the scientific and industrial community, most of the electrochemical characterization is carried out using poor reference electrodes or even no reference electrode. In this case, the performances of the active material are inaccurate, especially at high current densities. In this work we show the error committed in neglecting the polarizability of lithium counter electrodes, and we propose two reference electrodes to use in organic electrolytes based on lithium salts, namely Li4Ti5O12 and LiFePO 4. In particular, it was observed that, the polarizability of the metallic lithium counter electrode has a relevant stochastic component, which renders measurements at high current densities (above 1 mA·cm - 2) in two electrode cells non reproducible.

  11. Lithium metal oxide electrodes for lithium batteries

    Science.gov (United States)

    Thackeray, Michael M.; Kim, Jeom-Soo; Johnson, Christopher S.

    2008-01-01

    An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.xbatteries containing the electrodes.

  12. Hierarchically structured nanocarbon electrodes for flexible solid lithium batteries

    KAUST Repository

    Wei, Di

    2013-09-01

    The ever increasing demand for storage of electrical energy in portable electronic devices and electric vehicles is driving technological improvements in rechargeable batteries. Lithium (Li) batteries have many advantages over other rechargeable battery technologies, including high specific energy and energy density, operation over a wide range of temperatures (-40 to 70. °C) and a low self-discharge rate, which translates into a long shelf-life (~10 years) [1]. However, upon release of the first generation of rechargeable Li batteries, explosions related to the shorting of the circuit through Li dendrites bridging the anode and cathode were observed. As a result, Li metal batteries today are generally relegated to non-rechargeable primary battery applications, because the dendritic growth of Li is associated with the charging and discharging process. However, there still remain significant advantages in realizing rechargeable secondary batteries based on Li metal anodes because they possess superior electrical conductivity, higher specific energy and lower heat generation due to lower internal resistance. One of the most practical solutions is to use a solid polymer electrolyte to act as a physical barrier against dendrite growth. This may enable the use of Li metal once again in rechargeable secondary batteries [2]. Here we report a flexible and solid Li battery using a polymer electrolyte with a hierarchical and highly porous nanocarbon electrode comprising aligned multiwalled carbon nanotubes (CNTs) and carbon nanohorns (CNHs). Electrodes with high specific surface area are realized through the combination of CNHs with CNTs and provide a significant performance enhancement to the solid Li battery performance. © 2013 Elsevier Ltd.

  13. Organometallic-inorganic hybrid electrodes for lithium-ion batteries

    Science.gov (United States)

    Huang, Qian; Lemmon, John P.; Choi, Daiwon; Cosimbescu, Lelia

    2016-09-13

    Disclosed are embodiments of active materials for organometallic and organometallic-inorganic hybrid electrodes and particularly active materials for organometallic and organometallic-inorganic hybrid cathodes for lithium-ion batteries. In certain embodiments the organometallic material comprises a ferrocene polymer.

  14. Microwave synthesis of electrode materials for lithium batteries

    Indian Academy of Sciences (India)

    M Harish Bhat; B P Chakravarthy; P A Ramakrishnan; A Levasseur; K J RAO

    2000-12-01

    A novel microwave method is described for the preparation of electrode materials required for lithium batteries. The method is simple, fast and carried out in most cases with the same starting material as in conventional methods. Good crystallinity has been noted and lower temperatures of reaction has been inferred in cases where low temperature products have been identified.

  15. A method for connecting electrodes in a storage battery

    Energy Technology Data Exchange (ETDEWEB)

    Sakurai, T.; Nakadzima, T.; Toda, K.

    1983-07-14

    Groups of electrodes are placed in the body of a storage battery (AB) divided by partitions. The storage cells are connected using connecting elements passed through openings in the partitions. The elements to be connected are heated with pressure which melts them.

  16. Lithium sulfide compositions for battery electrolyte and battery electrode coatings

    Science.gov (United States)

    Liang, Chengdu; Liu, Zengcai; Fu, Wunjun; Lin, Zhan; Dudney, Nancy J; Howe, Jane Y; Rondinone, Adam J

    2013-12-03

    Methods of forming lithium-containing electrolytes are provided using wet chemical synthesis. In some examples, the lithium containing electroytes are composed of .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7. The solid electrolyte may be a core shell material. In one embodiment, the core shell material includes a core of lithium sulfide (Li.sub.2S), a first shell of .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7, and a second shell including one or .beta.-Li.sub.3PS.sub.4 or Li.sub.4P.sub.2S.sub.7 and carbon. The lithium containing electrolytes may be incorporated into wet cell batteries or solid state batteries.

  17. High voltage and high specific capacity dual intercalating electrode Li-ion batteries

    Science.gov (United States)

    West, William C. (Inventor); Blanco, Mario (Inventor)

    2010-01-01

    The present invention provides high capacity and high voltage Li-ion batteries that have a carbonaceous cathode and a nonaqueous electrolyte solution comprising LiF salt and an anion receptor that binds the fluoride ion. The batteries can comprise dual intercalating electrode Li ion batteries. Methods of the present invention use a cathode and electrode pair, wherein each of the electrodes reversibly intercalate ions provided by a LiF salt to make a high voltage and high specific capacity dual intercalating electrode Li-ion battery. The present methods and systems provide high-capacity batteries particularly useful in powering devices where minimizing battery mass is important.

  18. Toward Uniformly Dispersed Battery Electrode Composite Materials: Characteristics and Performance.

    Science.gov (United States)

    Kwon, Yo Han; Huie, Matthew M; Choi, Dalsu; Chang, Mincheol; Marschilok, Amy C; Takeuchi, Kenneth J; Takeuchi, Esther S; Reichmanis, Elsa

    2016-02-10

    Battery electrodes are complex mesoscale systems comprised of electroactive components, conductive additives, and binders. In this report, methods for processing electrodes with dispersion of the components are described. To investigate the degree of material dispersion, a spin-coating technique was adopted to provide a thin, uniform layer that enabled observation of the morphology. Distinct differences in the distribution profile of the electrode components arising from individual materials physical affinities were readily identified. Hansen solubility parameter (HSP) analysis revealed pertinent surface interactions associated with materials dispersivity. Further studies demonstrated that HSPs can provide an effective strategy to identify surface modification approaches for improved dispersions of battery electrode materials. Specifically, introduction of surfactantlike functionality such as oleic acid (OA) capping and P3HT-conjugated polymer wrapping on the surface of nanomaterials significantly enhanced material dispersity over the composite electrode. The approach to the surface treatment on the basis of HSP study can facilitate design of composite electrodes with uniformly dispersed morphology and may contribute to enhancing their electrical and electrochemical behaviors. The conductivity of the composites and their electrochemical performance was also characterized. The study illustrates the importance of considering electronic conductivity, electron transfer, and ion transport in the design of environments incorporating active nanomaterials.

  19. High efficiency iron electrode and additives for use in rechargeable iron-based batteries

    Energy Technology Data Exchange (ETDEWEB)

    Narayan, Sri R.; Prakash, G. K. Surya; Aniszfeld, Robert; Manohar, Aswin; Malkhandi, Souradip; Yang, Bo

    2017-02-21

    An iron electrode and a method of manufacturing an iron electrode for use in an iron-based rechargeable battery are disclosed. In one embodiment, the iron electrode includes carbonyl iron powder and one of a metal sulfide additive or metal oxide additive selected from the group of metals consisting of bismuth, lead, mercury, indium, gallium, and tin for suppressing hydrogen evolution at the iron electrode during charging of the iron-based rechargeable battery. An iron-air rechargeable battery including an iron electrode comprising carbonyl iron is also disclosed, as is an iron-air battery wherein at least one of the iron electrode and the electrolyte includes an organosulfur additive.

  20. Rechargeable aluminum batteries with conducting polymers as positive electrodes.

    Energy Technology Data Exchange (ETDEWEB)

    Hudak, Nicholas S.

    2013-12-01

    This report is a summary of research results from an Early Career LDRD project con-ducted from January 2012 to December 2013 at Sandia National Laboratories. Demonstrated here is the use of conducting polymers as active materials in the posi-tive electrodes of rechargeable aluminum-based batteries operating at room tempera-ture. The battery chemistry is based on chloroaluminate ionic liquid electrolytes, which allow reversible stripping and plating of aluminum metal at the negative elec-trode. Characterization of electrochemically synthesized polypyrrole films revealed doping of the polymers with chloroaluminate anions, which is a quasi-reversible reac-tion that facilitates battery cycling. Stable galvanostatic cycling of polypyrrole and polythiophene cells was demonstrated, with capacities at near-theoretical levels (30-100 mAh g-1) and coulombic efficiencies approaching 100%. The energy density of a sealed sandwich-type cell with polythiophene at the positive electrode was estimated as 44 Wh kg-1, which is competitive with state-of-the-art battery chemistries for grid-scale energy storage.

  1. Electrochemistry of Some New Alkaline Battery Electrodes

    Science.gov (United States)

    1976-02-01

    Charging Efficiencies for AFAPL and Aircraft Cells 20 4. Slow Scan Cyclic Voltametry of 30% KOH Solutions at the Nickel Hydroxide Electrode 21 5...in our laboratory has offered a partial explanation for this effect. Using cyclic voltametric studies it was revealed that presence of cobalt...observed between charge and discharge peak potentials. In the presence of Ca. 10% cobalt hydroxide, this difference is only 75 mV. The cyclic voltametric

  2. Multi-component intermetallic electrodes for lithium batteries

    Science.gov (United States)

    Thackeray, Michael M; Trahey, Lynn; Vaughey, John T

    2015-03-10

    Multi-component intermetallic negative electrodes prepared by electrochemical deposition for non-aqueous lithium cells and batteries are disclosed. More specifically, the invention relates to composite intermetallic electrodes comprising two or more compounds containing metallic or metaloid elements, at least one element of which can react with lithium to form binary, ternary, quaternary or higher order compounds, these compounds being in combination with one or more other metals that are essentially inactive toward lithium and act predominantly, but not necessarily exclusively, to the electronic conductivity of, and as current collection agent for, the electrode. The invention relates more specifically to negative electrode materials that provide an operating potential between 0.05 and 2.0 V vs. metallic lithium.

  3. Characterization of gas diffusion electrodes for metal-air batteries

    Science.gov (United States)

    Danner, Timo; Eswara, Santhana; Schulz, Volker P.; Latz, Arnulf

    2016-08-01

    Gas diffusion electrodes are commonly used in high energy density metal-air batteries for the supply of oxygen. Hydrophobic binder materials ensure the coexistence of gas and liquid phase in the pore network. The phase distribution has a strong influence on transport processes and electrochemical reactions. In this article we present 2D and 3D Rothman-Keller type multiphase Lattice-Boltzmann models which take into account the heterogeneous wetting behavior of gas diffusion electrodes. The simulations are performed on FIB-SEM 3D reconstructions of an Ag model electrode for predefined saturation of the pore space with the liquid phase. The resulting pressure-saturation characteristics and transport correlations are important input parameters for modeling approaches on the continuum scale and allow for an efficient development of improved gas diffusion electrodes.

  4. Metal | polypyrrole battery with the air regenerated positive electrode

    Science.gov (United States)

    Grgur, Branimir N.

    2014-12-01

    Recharge characteristics of the battery based on the electrochemically synthesized polypyrrole cathode and aluminum, zinc, or magnesium anode in 2 M NH4Cl are investigated. It is shown that polypyrrole electrode can be regenerated by the reoxidation with the dissolved oxygen from the air. Using the polypyrrole synthesized on high surface graphite-felt electrode under modest discharge conditions, stable discharge voltage of 1.1 V is obtained. Such behavior is explained by the complex interaction of polypyrrole and hydrogen peroxide produced by the oxygen reduction reaction. The electrochemical characteristics are compared with the zinc-manganese dioxide and zinc-air systems.

  5. Electrochemical Impedance of a Battery Electrode with Anisotropic Active Particles

    CERN Document Server

    Song, J

    2013-01-01

    Electrochemical impedance spectra for battery electrodes are usually interpreted using models that assume isotropic active particles, having uniform current density and symmetric diffusivities. While this can be reasonable for amorphous or polycrystalline materials with randomly oriented grains, modern electrode materials increasingly consist of highly anisotropic, single-crystalline, nanoparticles, with different impedance characteristics. In this paper, analytical expressions are derived for the impedance of anisotropic particles with tensorial diffusivities and orientation-dependent surface reaction rates and capacitances. The resulting impedance spectrum contains clear signatures of the anisotropic material properties and aspect ratio, as well as statistical variations in any of these parameters.

  6. A device for forming storage battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Yasuda, K.; Inaba, Y.; Kitamura, E.; Oda, S.; Ota, K.

    1983-07-20

    The compound, which basically contains CdO, is continuously applied to a base strip which has a porous structure. The strip is passed along the surface of a roller, on the surface of which cylindrical electricity conducting rods are installed in a direction transverse to the length of the strip. The rods have axles parallel to the roller axis. The diameter of the rods is one tenth to one twentieth of the diameter of the roller. The length of the rods is greater than the width of the strip. The electrodes are formed at a current with a density of approximately 170 milliamperes per square centimeter.

  7. Azimuthal swirl in liquid metal electrodes and batteries

    Science.gov (United States)

    Ashour, Rakan; Kelley, Douglas

    2016-11-01

    Liquid metal batteries consist of two molten metals with different electronegativity separated by molten salt. In these batteries, critical performance related factors such as the limiting current density are governed by fluid mixing in the positive electrode. In this work we present experimental results of a swirling flow in a layer of molten lead-bismuth alloy driven by electrical current. Using in-situ ultrasound velocimetery, we show that poloidal circulation appears at low current density, whereas azimuthal swirl becomes dominant at higher current density. The presence of thermal gradients produces buoyant forces, which are found to compete with those produced by current injection. Taking the ratio of the characteristic electromagnetic to buoyant flow velocity, we are able to predict the current density at which the flow becomes electromagnetically driven. Scaling arguments are also used to show that swirl is generated through self-interaction between the electrical current in the electrode with its own magnetic field.

  8. A lithium electrode with a zinc substrate for secondary batteries

    Science.gov (United States)

    Matsuda, Y.; Morita, M.; Katsuma, H.

    1983-03-01

    Koch (1981) and Abraham (1982) have reported work concerning the development of a lithium secondary battery using an organic electrolyte. An efficient Li electrode is a vital factor in connection with the realization of the considered rechargeable batteries. In order to obtain good efficiency in charge-discharge cycling operations, it has been proposed to employ Li negative plates with metal substrates. High coulombic efficiency was achieved using an Al substrate, which forms an alloy with deposited Li during the period of charging. The present investigation is concerned with the charge-discharge characteristics of a Li electrode with a Zn substrate in propylene carbonate solution containing LiClO4 or LiBF4. It is found that the efficiency in the case of a plate with a Zn substrate, which alloys easily with deposited Li, is as high as that obtained in connection with the use of an Al substrate.

  9. Effect of Calendering on Electrode Wettability in Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Yangping eSheng

    2014-12-01

    Full Text Available Controlling the wettability between the porous electrode and the electrolyte in lithium ion batteries can improve both the manufacturing process and the electrochemical performance of the cell. The wetting rate, which is the electrolyte transport rate in the porous electrode, can be quantified using the wetting balance. The effect of the calendering process on the wettability of anode electrodes was investigated. A graphite anode film with an as-coated thickness of 59 μm was used as baseline electrode film and was calendered to produce films with thickness ranging from 55 to 41 µm. Results show that wettability is improved by light calendering from an initial thickness of 59 μm to a calendered thickness of 53 μm where the wetting rate increased from 0.375 to 0.589 mm/s0.5. Further calendering below 53 µm resulted in a decrease in wetting rates to a minimum observed value of 0.206 mm/s0.5 at a calendered thickness of 41 μm. Under the same electrolyte, wettability of the electrode is controlled to a great extent by the pore structure in the electrode film which includes parameters such as porosity, pore size distribution, pore geometry and topology. Relations between the wetting behavior and the pore structure as characterized by mercury intrusion and electron microscopy exist and can be used to manipulate the wetting behavior of electrodes.

  10. Nanostructured Ion Storage Electrode Materials for Lithium Batteries and Supercapacitors

    Institute of Scientific and Technical Information of China (English)

    S.R.S.Prabaharan

    2007-01-01

    1 Results Performance of lithium-ion batteries, electrochemical capacitors, and other electric-energy storage devices is not only determined simply by macroscopic chemical composition of their electrode, but also strongly affected by shape and size of the active materials. Nanostructured materials are distinguished from conventional polycrystalline materials by the nanometer size of the structural units that compose them, and they often exhibit properties that are drastically different from the conventi...

  11. Understanding electrode materials of rechargeable lithium batteries via DFT calculations

    Institute of Scientific and Technical Information of China (English)

    Tianran Zhang; Daixin Li; Zhanliang Tao; Jun Chenn

    2013-01-01

    Rechargeable lithium batteries have achieved a rapid advancement and commercialization in the past decade owing to their high capacity and high power density. Different functional materials have been put forward progressively, and each possesses distinguishing structural features and electrochemical properties. In virtue of density functional theory (DFT) calculations, we can start from a specific structure to get a deep comprehension and accurate prediction of material properties and reaction mechanisms. In this paper, we review the main progresses obtained by DFT calculations in the electrode materials of rechargeable lithium batteries, aiming at a better understanding of the common electrode materials and gaining insights into the battery performance. The applications of DFT calculations involve in the following points of crystal structure modeling and stability investigations of delithiated and lithiated phases, average lithium intercalation voltage, prediction of charge distributions and band structures, and kinetic studies of lithium ion diffusion processes, which can provide atomic understanding of the capacity, reaction mechanism, rate capacity, and cycling ability. The results obtained from DFT are valuable to reveal the relationship between the structure and the properties, promoting the design of new electrode materials.

  12. High-performance battery electrodes via magnetic templating

    Science.gov (United States)

    Sander, J. S.; Erb, R. M.; Li, L.; Gurijala, A.; Chiang, Y.-M.

    2016-08-01

    In lithium-ion batteries, the critical need for high-energy-density, low-cost storage for applications ranging from wearable computing to megawatt-scale stationary storage has created an unmet need for facile methods to produce high-density, low-tortuosity, kinetically accessible storage electrodes. Here we show that magnetic control of sacrificial features enables the creation of directional pore arrays in lithium-ion electrodes. The directional pores result in faster charge transport kinetics and enable electrodes with more than threefold higher area capacity (for example, >12 mAh cm-2 versus charge-discharge rates. We demonstrate these capabilities in laboratory cells under various test conditions, including an electric vehicle model drive cycle.

  13. Advanced Electrodes for High Power Li-ion Batteries

    Directory of Open Access Journals (Sweden)

    Christian M. Julien

    2013-03-01

    Full Text Available While little success has been obtained over the past few years in attempts to increase the capacity of Li-ion batteries, significant improvement in the power density has been achieved, opening the route to new applications, from hybrid electric vehicles to high-power electronics and regulation of the intermittency problem of electric energy supply on smart grids. This success has been achieved not only by decreasing the size of the active particles of the electrodes to few tens of nanometers, but also by surface modification and the synthesis of new multi-composite particles. It is the aim of this work to review the different approaches that have been successful to obtain Li-ion batteries with improved high-rate performance and to discuss how these results prefigure further improvement in the near future.

  14. Development of a benchmarking model for lithium battery electrodes

    Science.gov (United States)

    Bergholz, Timm; Korte, Carsten; Stolten, Detlef

    2016-07-01

    This paper presents a benchmarking model to enable systematic selection of anode and cathode materials for lithium batteries in stationary applications, hybrid and battery electric vehicles. The model incorporates parameters for energy density, power density, safety, lifetime, costs and raw materials. Combinations of carbon anodes, Li4Ti5O12 or TiO2 with LiFePO4 cathodes comprise interesting combinations for application in hybrid power trains. Higher cost and raw material prioritization of stationary applications hinders the breakthrough of Li4Ti5O12, while a combination of TiO2 and LiFePO4 is suggested. The favored combinations resemble state-of-the-art materials, whereas novel cell chemistries must be optimized for cells in battery electric vehicles. In contrast to actual research efforts, sulfur as a cathode material is excluded due to its low volumetric energy density and its known lifetime and safety issues. Lithium as anode materials is discarded due to safety issues linked to electrode melting and dendrite formation. A high capacity composite Li2MnO3·LiNi0.5Co0.5O2 and high voltage spinel LiNi0.5Mn1.5O4 cathode with silicon as anode material promise high energy densities with sufficient lifetime and safety properties if electrochemical and thermal stabilization of the electrolyte/electrode interfaces and bulk materials is achieved. The model allows a systematic top-down orientation of research on lithium batteries.

  15. A method for connecting electrodes in a storage battery

    Energy Technology Data Exchange (ETDEWEB)

    Toda, K.; Karasava, S.

    1983-07-14

    Groups of electrodes are placed into a common casing for the storage battery (AB) divided by partitions. The groups are electrically connected, inserting connecting elements into openings in the partitions and melting them with compression and heating. One of the connecting elements is made in the form of a cylinder with a flat face, while the other is made in the form of a cylinder with a head which has the form of a segment turned by its convex side towards the flat face of the first cylinder in the cross section.

  16. Composite Metal-hydrogen Electrodes for Metal-Hydrogen Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Ruckman, M W; Wiesmann, H; Strongin, M; Young, K; Fetcenko, M

    1997-04-01

    The purpose of this project is to develop and conduct a feasibility study of metallic thin films (multilayered and alloy composition) produced by advanced sputtering techniques for use as anodes in Ni-metal hydrogen batteries. The anodes could be incorporated in thin film solid state Ni-metal hydrogen batteries that would be deposited as distinct anode, electrolyte and cathode layers in thin film devices. The materials could also be incorporated in secondary consumer batteries (i.e. type AF(4/3 or 4/5)) which use electrodes in the form of tapes. The project was based on pioneering studies of hydrogen uptake by ultra-thin Pd-capped metal-hydrogen ratios exceeding and fast hydrogen charging and Nb films, these studies suggested that materials with those of commercially available metal hydride materials discharging kinetics could be produced. The project initially concentrated on gas phase and electrochemical studies of Pd-capped niobium films in laboratory-scale NiMH cells. This extended the pioneering work to the wet electrochemical environment of NiMH batteries and exploited advanced synchrotron radiation techniques not available during the earlier work to conduct in-situ studies of such materials during hydrogen charging and discharging. Although batteries with fast charging kinetics and hydrogen-metal ratios approaching unity could be fabricated, it was found that oxidation, cracking and corrosion in aqueous solutions made pure Nb films-and multiiayers poor candidates for battery application. The project emphasis shifted to alloy films based on known elemental materials used for NiMH batteries. Although commercial NiMH anode materials contain many metals, it was found that 0.24 µm thick sputtered Zr-Ni films cycled at least 50 times with charging efficiencies exceeding 95% and [H]/[M] ratios of 0.7-1.0. Multilayered or thicker Zr-Ni films could be candidates for a thin film NiMH battery that may have practical applications as an integrated power source for

  17. Phase transitions in insertion electrodes for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Thackeray, M. M.

    2000-02-02

    Phase transitions that occur during lithium insertion into layered and framework structures are discussed in the context of their application as positive and negative electrodes in lithium-ion batteries. The discussion is focused on the two-dimensional structures of graphite, LiNi{sub 1{minus}x}M{sub x}O{sub 2} (M = Co, Ti and Mg), and Li{sub 1.2}V{sub 3}O{sub 8}; examples of framework structures with a three-dimensional interstitial space for Li{sup +}-ion transport include the spinel oxides and intermetallic compounds with zinc-blende-type structures. The phase transitions are discussed in terms of their tolerance to lithium insertion and extraction and to the chemical stability of the electrodes in the cell environment.

  18. Electrochemical Techniques for Intercalation Electrode Materials in Rechargeable Batteries.

    Science.gov (United States)

    Zhu, Yujie; Gao, Tao; Fan, Xiulin; Han, Fudong; Wang, Chunsheng

    2017-03-16

    Understanding of the thermodynamic and kinetic properties of electrode materials is of great importance to develop new materials for high performance rechargeable batteries. Compared with computational understanding of physical and chemical properties of electrode materials, experimental methods provide direct and convenient evaluation of these properties. Often, the information gained from experimental work can not only offer feedback for the computational methods but also provide useful insights for improving the performance of materials. However, accurate experimental quantification of some properties can still be challenging. Among them, chemical diffusion coefficient is one representative example. It is one of the most crucial parameters determining the kinetics of intercalation compounds, which are by far the dominant electrode type used in rechargeable batteries. Therefore, it is of significance to quantitatively evaluate this parameter. For this purpose, various electrochemical techniques have been invented, for example, galvanostatic intermittent titration technique (GITT), potentiostatic intermittent titration technique (PITT), electrochemical impedance spectroscopy (EIS), and cyclic voltammetry (CV). One salient advantage of these electrochemical techniques over other characterization techniques is that some implicit thermodynamic and kinetic quantities can be linked with the readily measurable electrical signals, current, and voltage, with very high precision. Nevertheless, proper application of these techniques requires not just an understanding of the structure and chemistry of the studied materials but sufficient knowledge of the physical model for ion transport within solid host materials and the analysis method to solve for chemical diffusion coefficient. Our group has been focusing on using various electrochemical techniques to investigate battery materials, as well as developing models for studying some emerging materials. In this Account, the

  19. Improved Positive Electrode Materials for Lithium-ion Batteries

    Science.gov (United States)

    Conry, Thomas Edward

    The introduction of the first commercially produced Li-ion battery by Sony in 1990 sparked a period of unprecedented growth in the consumer electronics industry. Now, with increasing efforts to move away from fossil-fuel-derived energy sources, a substantial amount of current research is focused on the development of an electrified transportation fleet. Unfortunately, existent battery technologies are unable to provide the necessary performance for electric vehicles (EV's) and plug-in hybrid electric vehicles (PHEV's) vehicles at a competitive cost. The cost and performance metrics of current Li-ion batteries are mainly determined by the positive electrode materials. The work here is concerned with understanding the structural and electrochemical consequences of cost-lowering mechanisms in two separate classes of Li-ion cathode materials; the LiMO2 (M = Ni, Mn, Co) layered oxides and the LiMPO4 olivine materials; with the goal of improving performance. Al-substitution for Co in LiNizMnzCo1-2zO 2 ("NMC") materials not only decreases the costly Co-content, but also improves the safety aspects and, notably, enhances the cycling stability of the layered oxide electrodes. The structural and electrochemical effects of Al-substitution are investigated here in a model NMC compound, LiNi0.45 Mn0.45Co0.1-yAlyO2. In addition to electrochemical measurements, various synchrotron-based characterization methods are utilized, including high-resolution X-ray diffraction (XRD), in situ X-ray diffraction, and X-ray absorption spectroscopy (XAS). Al-substitution causes a slight distortion of the as-synthesized hexagonal layered oxide lattice, lowering the inherent octahedral strain within the transition metal layer. The presence of Al also is observed to limit the structural variation of the NMC materials upon Li-deintercalation, as well as extended cycling of the electrodes. Various olivine materials, LiMPO4 ( M=Fe,Co) are produced using a custom-built spray pyrolysis system. Spray

  20. Fabrication of a three-electrode battery using hydrogen-storage materials

    Science.gov (United States)

    Roh, Chi-Woo; Seo, Jung-Yong; Moon, Hyung-Seok; Park, Hyun-Young; Nam, Na-Yun; Cho, Sung Min; Yoo, Pil J.; Chung, Chan-Hwa

    2015-04-01

    In this study, an energy storage device using a three-electrode battery is fabricated. The charging process takes place during electrolysis of the alkaline electrolyte where hydrogen is stored at the palladium bifunctional electrode. Upon discharging, power is generated by operating the alkaline fuel cell using hydrogen which is accumulated in the palladium hydride bifunctional electrode during the charging process. The bifunctional palladium electrode is prepared by electrodeposition using a hydrogen bubble template followed by a galvanic displacement reaction of platinum in order to functionalize the electrode to work not only as a hydrogen storage material but also as an anode in a fuel cell. This bifunctional electrode has a sufficiently high surface area and the platinum catalyst populates at the surface of electrode to operate the fuel cell. The charging and discharging performance of the three-electrode battery are characterized. In addition, the cycle stability is investigated.

  1. Effect of surface modification of metal hydride electrode on performance of MH/Ni batteries

    Institute of Scientific and Technical Information of China (English)

    YANG Kai; WU Feng; CHEN Shi; ZHANG Cun-zhong

    2007-01-01

    A novel method was applied to the surface modification of the metal hydride(MH) electrode of MH/Ni batteries. Both sides of the electrode were plated with a thin silver film about 0.1μm thick using vacuum evaporation plating technology, and the effect of the electrode on the performance of MH/Ni batteries was examined. It is found that the surface modification can enhance the electrode conductivity and decrease the battery ohimic resistance. After surface modification, the discharge capacity at 5C (7.5A) is increased by 212 mA·h and the discharge voltage is increased by 0.11 V, the resistance of the batteries is also decreased by 32%. The batteries with modified electrode exhibit satisfactory durability. The remaining capacity of the modified batteries is 89% of the initial capacity even after 500 cycles. The inner pressure of the batteries during overcharging is lowered and the charging efficiency of the batteries is improved.

  2. Organic Materials as Electrodes for Li-ion Batteries

    Science.gov (United States)

    2015-09-04

    Several organic compounds were synthesized , characterized and tested in battery configurations. The details are given for each class of materials...batteries. Several organic compounds were synthesized , characterized and tested in battery configurations. The details are given for each class of materials... synthesized , characterized and tested in battery configurations. The details are given below for each class of materials.Various macrocycles, their synthesis

  3. Recent research progress on iron- and manganese-based positive electrode materials for rechargeable sodium batteries.

    Science.gov (United States)

    Yabuuchi, Naoaki; Komaba, Shinichi

    2014-08-01

    Large-scale high-energy batteries with electrode materials made from the Earth-abundant elements are needed to achieve sustainable energy development. On the basis of material abundance, rechargeable sodium batteries with iron- and manganese-based positive electrode materials are the ideal candidates for large-scale batteries. In this review, iron- and manganese-based electrode materials, oxides, phosphates, fluorides, etc, as positive electrodes for rechargeable sodium batteries are reviewed. Iron and manganese compounds with sodium ions provide high structural flexibility. Two layered polymorphs, O3- and P2-type layered structures, show different electrode performance in Na cells related to the different phase transition and sodium migration processes on sodium extraction/insertion. Similar to layered oxides, iron/manganese phosphates and pyrophosphates also provide the different framework structures, which are used as sodium insertion host materials. Electrode performance and reaction mechanisms of the iron- and manganese-based electrode materials in Na cells are described and the similarities and differences with lithium counterparts are also discussed. Together with these results, the possibility of the high-energy battery system with electrode materials made from only Earth-abundant elements is reviewed.

  4. Nanostructured Lead Compounds in Electrode Materials of a Lead-Acid Battery

    Directory of Open Access Journals (Sweden)

    A.P. Kuzmenko

    2016-11-01

    Full Text Available The nanostructure and phase composition of the electrode material of lead-acid batteries, formed by chemical transformations with involvement of sulfuric acid solutions of various concentrations, water and carbon dioxide have been studied.

  5. Surface modifications of electrode materials for lithium ion batteries

    Science.gov (United States)

    Fu, L. J.; Liu, H.; Li, C.; Wu, Y. P.; Rahm, E.; Holze, R.; Wu, H. Q.

    2006-02-01

    Since the birth of the lithium ion battery in the early 1990s, its development has been very rapid and it has been widely applied as power source for a lot of light and high value electronics due to its significant advantages over traditional rechargeable battery systems. Recent research demonstrates the importance of surface structural features of electrode materials for their electrochemical performance, and in this paper the latest progress on this aspect is reviewed. Electrode materials are either anodic or cathodic ones. The former mainly include graphitic carbons, whose surfaces can be modified by mild oxidation, deposition of metals and metal oxides, coating with polymers and other kinds of carbons. Through these modifications, the surface structures of the graphitic carbon anodes are improved, and these improvements include: (1) smoothing the active edge surfaces by removing some reactive sites and/or defects on the graphite surface, (2) forming a dense oxide layer on the graphite surface, and (3) covering active edge structures on the graphite surface. Meanwhile, other accompanying changes occur: (1) production of nanochannels/micropores, (2) an increase in the electronic conductivity, (3) an inhibition of structural changes during cycling, (4) a reduction of the thickness of the SEI (solid-electrolyte-interface) layer, and (5) an increase in the number of host sites for lithium storage. As a result, the direct contact of graphite with the electrolyte solution is prevented, its surface reactivity with electrolytes, the decomposition of electrolytes, the co-intercalation of the solvated lithium ions and the charge-transfer resistance are decreased, and the movement of graphene sheets is inhibited. When the surfaces of cathode materials, mainly including LiCoO 2, LiNiO 2 and LiMn 2O 4, are coated with oxides such as MgO, Al 2O 3, ZnO, SnO 2, ZrO 2, Li 2Oṡ2B 2O 3 glass and other electroactive oxides, the coating can prevent their direct contact with the

  6. Communications: Elementary oxygen electrode reactions in the aprotic Li-air battery

    Science.gov (United States)

    Hummelshøj, J. S.; Blomqvist, J.; Datta, S.; Vegge, T.; Rossmeisl, J.; Thygesen, K. S.; Luntz, A. C.; Jacobsen, K. W.; Nørskov, J. K.

    2010-02-01

    We discuss the electrochemical reactions at the oxygen electrode of an aprotic Li-air battery. Using density functional theory to estimate the free energy of intermediates during the discharge and charge of the battery, we introduce a reaction free energy diagram and identify possible origins of the overpotential for both processes. We also address the question of electron conductivity through the Li2O2 electrode and show that in the presence of Li vacancies Li2O2 becomes a conductor.

  7. Benefits of Nanostructuring Electrodes for High-Energy and High-Power Lithium Batteries

    Institute of Scientific and Technical Information of China (English)

    Joachim; Maier

    2007-01-01

    1 Results One of the greatest challenges for our society is providing powerful electrochemical energy storage devices with both high energy and high power densities. Rechargeable lithium-based batteries are amongst the most promising candidates in terms of energy density,the achievement of high power density is hindered by kinetic problems of the electrode materials.This contribution that emphasizes the power of nanostructuring for electrodes in lithium-based batteries,deals with several nanostructured ...

  8. Thick electrodes for Li-ion batteries: A model based analysis

    OpenAIRE

    2016-01-01

    Li-ion batteries are commonly used in portable electronic devices due to their outstanding energy and power density. A remaining issue which hinders the breakthrough e.g. in the automotive sector is the high production cost. For low power applications, such as stationary storage, batteries with electrodes thicker than 300 \\textmu m were suggested. High energy densities can be attained with only a few electrode layers which reduces production time and cost. However, mass and charge transpor...

  9. Communications: Elementary oxygen electrode reactions in the aprotic Li-air battery

    DEFF Research Database (Denmark)

    Hummelshøj, Jens Strabo; Blomquist, Jakob; Datta, Soumendu;

    2010-01-01

    We discuss the electrochemical reactions at the oxygen electrode of an aprotic Li-air battery. Using density functional theory to estimate the free energy of intermediates during the discharge and charge of the battery, we introduce a reaction free energy diagram and identify possible origins...

  10. Development of Nanoporous Carbide-Derived Carbon Electrodes for High-Performance Lithium-Ion Batteries

    Science.gov (United States)

    2011-09-01

    Advanced Energy Materials, vol. 22, pp. E28-E62, 2010. [2] D. Linden and T. B. Reddy, Handbook of Batteries , 3rd. New York: McGraw-Hill, 2002...Electrodes for High-Performance Lithium-Ion Batteries 5. FUNDING NUMBERS 6. AUTHOR( S ) Kamryn M. Sakamoto 7. PERFORMING ORGANIZATION NAME( S ) AND...5 accumulations, each at ~30 s ). 36 C. MACCOR BATTERY TESTER The button-type coin cells that were constructed were tested and cycled. The

  11. Particulate inverse opal carbon electrodes for lithium-ion batteries.

    Science.gov (United States)

    Kang, Da-Young; Kim, Sang-Ok; Chae, Yu Jin; Lee, Joong Kee; Moon, Jun Hyuk

    2013-01-29

    Inverse opal carbon materials were used as anodes for lithium ion batteries. We applied particulate inverse opal structures and their dispersion in the formation of anode electrodes via solution casting. We prepared aminophenyl-grafted inverse opal carbons (a-IOC), inverse opal carbons with mesopores (mIOC), and bare inverse opal carbons (IOC) and investigated the electrochemical behavior of these samples as anode materials. Surface modification by aminophenyl groups was confirmed by XPS measurements. TEM images showed mesopores, and the specific area of mIOC was compared with that of IOC using BET analysis. A half-cell test was performed to compare a-IOC with IOC and mIOC with IOC. In the case of the a-IOC structure, the cell test revealed no improvement in the reversible specific capacity or the cycle performance. The mIOC cell showed a reversible specific capacity of 432 mAh/g, and the capacity was maintained at 88%-approximately 380 mAh/g-over 20 cycles.

  12. Battery electrodes: Properties and performance. (Latest citations from the EI Compendex*plus database). Published Search

    Energy Technology Data Exchange (ETDEWEB)

    NONE

    1996-12-01

    The bibliography contains citations concerning battery electrodes relative to research and development. Topics discuss electrode technology, chemical solutions, materials improvement, reactions, and rechargeability and reliability. Electrochemical and thermodynamic characteristics, materials testing and evaluation, and corrosion protection are also included. (Contains 50-250 citations and includes a subject term index and title list.) (Copyright NERAC, Inc. 1995)

  13. Surface modification of battery electrodes via electroless deposition with improved performance for Na-ion batteries.

    Science.gov (United States)

    Lahiri, Abhishek; Olschewski, Mark; Gustus, René; Borisenko, Natalia; Endres, Frank

    2016-06-01

    Sodium-ion batteries (SIBs) are emerging as potential stationary energy storage devices due to the abundance and low cost of sodium. A simple and energy efficient strategy to develop electrodes for SIBs with a high charge/discharge rate is highly desirable. Here we demonstrate that by surface modification of Ge, using electroless deposition in SbCl3/ionic liquids, the stability and performance of the anode can be improved. This is due to the formation of GexSb1-x at the surface leading to better diffusion of Na, and the formation of a stable twin organic and inorganic SEI which protects the electrode. By judicious control of the surface modification, an improvement in the capacity to between 50% and 300% has been achieved at high current densities (0.83-8.4 A g(-1)) in an ionic liquid electrolyte NaFSI-[Py1,4]FSI. The results clearly demonstrate that an electroless deposition based surface modification strategy in ionic liquids offers exciting opportunities in developing superior energy storage devices.

  14. Gradient porous electrode architectures for rechargeable metal-air batteries

    Energy Technology Data Exchange (ETDEWEB)

    Dudney, Nancy J.; Klett, James W.; Nanda, Jagjit; Narula, Chaitanya Kumar; Pannala, Sreekanth

    2016-03-22

    A cathode for a metal air battery includes a cathode structure having pores. The cathode structure has a metal side and an air side. The porosity decreases from the air side to the metal side. A metal air battery and a method of making a cathode for a metal air battery are also disclosed.

  15. Effect of Calendering on Electrode Wettability in Lithium-Ion Batteries

    OpenAIRE

    Yangping eSheng; Christopher R. Fell; Yong Kyu Son; Bernhard M. Metz; Junwei eJiang; Benjamin C. Church

    2014-01-01

    Controlling the wettability between the porous electrode and the electrolyte in lithium-ion batteries can improve both the manufacturing process and the electrochemical performance of the cell. The wetting rate, which is the electrolyte transport rate in the porous electrode, can be quantified using the wetting balance. The effect of the calendering process on the wettability of anode electrodes was investigated. A graphite anode film with an as-coated thickness of 59 μm was used as baseline ...

  16. Consistency Research of Negative Electrode Pasting for MH/Ni High Power Battery

    Institute of Scientific and Technical Information of China (English)

    Zhang Zhong; Liu Dong; Cao Shengbiao; Li Jianping; Jia Chunming

    2004-01-01

    It is discovered that the consistency of negative electrode is one of the main influences on battery performance, since the main raw material in negative electrode is metal hydride powder, ingredients, particle distribution and density of the powder could influence the pasting consistency in some aspects.With the study of MH powder characteristics, through the modification of the coating die, the consistency of negative electrode is improved efficiently.

  17. Nanostructured Composite Electrodes for Lithium Batteries (Final Technical Report)

    Energy Technology Data Exchange (ETDEWEB)

    Meilin Liu, James Gole

    2006-12-14

    The objective of this study was to explore new ways to create nanostructured electrodes for rechargeable lithium batteries. Of particular interests are unique nanostructures created by electrochemical deposition, etching and combustion chemical vapor deposition (CCVD). Three-dimensional nanoporous Cu6Sn5 alloy has been successfully prepared using an electrochemical co-deposition process. The walls of the foam structure are highly-porous and consist of numerous small grains. This represents a novel way of creating porous structures that allow not only fast transport of gas and liquid but also rapid electrochemical reactions due to high surface area. The Cu6Sn5 samples display a reversible capacity of {approx}400 mAhg-1. Furthermore, these materials exhibit superior rate capability. At a current drain of 10 mA/cm2(20C rate), the obtainable capacity was more than 50% of the capacity at 0.5 mA/cm2 (1C rate). Highly open and porous SnO2 thin films with columnar structure were obtained on Si/SiO2/Au substrates by CCVD. The thickness was readily controlled by the deposition time, varying from 1 to 5 microns. The columnar grains were covered by nanoparticles less than 20 nm. These thin film electrodes exhibited substantially high specific capacity. The reversible specific capacity of {approx}3.3 mAH/cm2 was demonstrated for up to 80 cycles at a charge/discharge rate of 0.3 mA/cm2. When discharged at 0.9 mA/cm2, the capacity was about 2.1 mAH/cm2. Tin dioxide box beams or tubes with square or rectangular cross sections were synthesized using CCVD. The cross-sectional width of the SnO2 tubules was tunable from 50 nm to sub-micrometer depending on synthesis temperature. The tubes are readily aligned in the direction perpendicular to the substrate surface to form tube arrays. Silicon wafers were electrochemically etched to produce porous silicon (PS) with honeycomb-type channels and nanoporous walls. The diameters of the channels are about 1 to 3 microns and the depth of the

  18. Study on microstructures of electrodes in lithium-ion batteries using variational multi-scale enrichment

    Science.gov (United States)

    Lee, Sangmin; Sastry, Ann Marie; Park, Jonghyun

    2016-05-01

    Performance and degradation of a Li-ion battery reflect the transport and kinetics of related species within the battery's electrode microstructures. The variational multi-scale principle is adapted to a Li-ion battery system in order to improve the predictions of battery performance by including multi-scale and multiphysics phenomena among the particle aggregates in the electrode; this physics cannot be addressed by conventional homogenized approaches. The developed model is verified through the direct numerical solutions and compared with the conventional pseudo-2D (P2D) model method. The developed model has revealed more dynamic battery behaviors related to the variation of the microstructure-such as particle shape, tortuosity, and material composition-while the corresponding result from P2D shows a monotonous change within different structures.

  19. Recovery Of Electrodic Powder From Spent Nickel-Metal Hydride Batteries (NiMH

    Directory of Open Access Journals (Sweden)

    Shin S.M.

    2015-06-01

    Full Text Available This study was focused on recycling process newly proposed to recover electrodic powder enriched in nickel (Ni and rare earth elements (La and Ce from spent nickel-metal hydride batteries (NiMH. In addition, this new process was designed to prevent explosion of batteries during thermal treatment under inert atmosphere. Spent nickel metal hydride batteries were heated over range of 300°C to 600°C for 2 hours and each component was completely separated inside reactor after experiment. Electrodic powder was successfully recovered from bulk components containing several pieces of metals through sieving operation. The electrodic powder obtained was examined by X-ray diffraction (XRD and energy dispersive X-ray spectroscopy (EDX and image of the powder was taken by scanning electron microscopy (SEM. It was finally found that nickel and rare earth elements were mainly recovered to about 45 wt.% and 12 wt.% in electrodic powder, respectively.

  20. Development of Magnesium-Insertion Positive Electrode for Rechargeable Magnesium Batteries

    Institute of Scientific and Technical Information of China (English)

    Huatang YUAN; Lifang JIAO; Jiansheng CAO; Xiusheng LIU; Ming ZHAO; Yongmei WANG

    2004-01-01

    Magnesium-based rechargeable batteries might be an interesting future alternative to lithium-based batteries. It is so far well known that Mg2+ ion insertion into ion-transfer hosts proceeds slowly compared with Li+, so it is necessary to realize fast Mg2+ transport in the host in addition to other requirements as practical cathode materials for magnesium batteries. Positive electrode materials based on inorganic transition-metal oxides, sulfides, and borides are the only ones used up to now to insert magnesium ions. In this paper, the available results of research on materials suitable as possible, for secondary magnesium batteries, are reviewed.

  1. High rate, long cycle life battery electrode materials with an open framework structure

    Energy Technology Data Exchange (ETDEWEB)

    Wessells, Colin; Huggins, Robert; Cui, Yi; Pasta, Mauro

    2015-02-10

    A battery includes a cathode, an anode, and an aqueous electrolyte disposed between the cathode and the anode and including a cation A. At least one of the cathode and the anode includes an electrode material having an open framework crystal structure into which the cation A is reversibly inserted during operation of the battery. The battery has a reference specific capacity when cycled at a reference rate, and at least 75% of the reference specific capacity is retained when the battery is cycled at 10 times the reference rate.

  2. Novel air electrode for metal-air battery with new carbon material and method of making same

    Science.gov (United States)

    Ross, P.N. Jr.

    1988-06-21

    This invention relates to a rechargeable battery or fuel cell. More particularly, this invention relates to a novel air electrode comprising a new carbon electrode support material and a method of making same. 3 figs.

  3. High Reversibility of Soft Electrode Materials in All-solid-state Batteries

    Directory of Open Access Journals (Sweden)

    Atsushi eSakuda

    2016-05-01

    Full Text Available All-solid-state batteries using inorganic solid electrolytes (SEs are considered to be ideal batteries for electric vehicles (EVs and plug-in hybrid electric vehicles (PHEVs because they are potentially safer than conventional lithium-ion batteries (LIBs. In addition, all-solid-state batteries are expected to have long battery lives owing to the inhibition of chemical side reactions because only lithium ions move through the typically used inorganic SEs. The development of high-energy (more than 300 Wh kg-1 secondary batteries has been eagerly anticipated for years. The application of high-capacity electrode active materials is essential for fabricating such batteries. Recently, we proposed metal polysulfides as new electrode materials. These materials show higher conductivity and density than sulfur, which is advantageous for fabricating batteries with relatively higher energy density. Lithium niobium sulfides, such as Li3NbS4, have relatively high density, conductivity, and rate capability among metal polysulfide materials, and batteries with these materials have capacities high enough to potentially exceed the gravimetric energy density of conventional LIBs.Favorable solid-solid contact between the electrode and electrolyte particles is a key factor for fabricating high performance all-solid-state batteries. Conventional oxide-based positive electrode materials tend to be given rise to cracks during fabrication and/or charge-discharge processes. Here we report all-solid-state cells using lithium niobium sulfide as a positive electrode material, where favorable solid-solid contact was established by using lithium sulfide electrode materials because of their high processability. Cracks were barely observed in the electrode particles in the all-solid-state cells before or after charging and discharging with a high capacity of approx. 400 mAh g-1, suggesting that the lithium niobium sulfide electrode charged and discharged without experiencing

  4. Evaluation of electrode materials for all-copper hybrid flow batteries

    Science.gov (United States)

    Leung, Puiki; Palma, Jesus; Garcia-Quismondo, Enrique; Sanz, Laura; Mohamed, M. R.; Anderson, Marc

    2016-04-01

    This work evaluates a number of two- and three-dimensional electrodes for the reactions of an all-copper hybrid flow battery. Half- and full-cell experiments are conducted by minimizing the crossover effect of the copper(II) species. The battery incorporates a Nafion® cation exchange membrane and the negative electrolyte is maintained at the monovalent (colourless) state by the incorporating copper turnings in the electrolyte reservoir. Under such conditions, the half-cell coulombic efficiencies of the negative electrode reactions are all higher than 90% regardless of electrode materials and the state-of-charge (SOC). With charge-discharge cycling the half-cell from a 0% SOC, the coulombic efficiencies of the positive electrode reactions are lower than 76% with the planar carbon electrode, which further decrease in shorter charge-discharge cycles. Polarization and half-cell charge-discharge experiments suggest that the high-surface-area electrodes effectively reduce the overpotentials and improve the coulombic efficiencies of both electrode reactions. When copper fibres and carbon felt are used as the negative and positive electrodes, the average coulombic and voltage efficiencies of an all-copper flow battery are as high as c.a. 99% and c.a. 60% at 50 mA cm-2 for 35 cycles.

  5. Lithium-free transition metal monoxides for positive electrodes in lithium-ion batteries

    Science.gov (United States)

    Jung, Sung-Kyun; Kim, Hyunchul; Cho, Min Gee; Cho, Sung-Pyo; Lee, Byungju; Kim, Hyungsub; Park, Young-Uk; Hong, Jihyun; Park, Kyu-Young; Yoon, Gabin; Seong, Won Mo; Cho, Yongbeom; Oh, Myoung Hwan; Kim, Haegyeom; Gwon, Hyeokjo; Hwang, Insang; Hyeon, Taeghwan; Yoon, Won-Sub; Kang, Kisuk

    2017-01-01

    Lithium-ion batteries based on intercalation compounds have dominated the advanced portable energy storage market. The positive electrode materials in these batteries belong to a material group of lithium-conducting crystals that contain redox-active transition metal and lithium. Materials without lithium-conducting paths or lithium-free compounds could be rarely used as positive electrodes due to the incapability of reversible lithium intercalation or the necessity of using metallic lithium as negative electrodes. These constraints have significantly limited the choice of materials and retarded the development of new positive electrodes in lithium-ion batteries. Here, we demonstrate that lithium-free transition metal monoxides that do not contain lithium-conducting paths in their crystal structure can be converted into high-capacity positive electrodes in the electrochemical cell by initially decorating the monoxide surface with nanosized lithium fluoride. This unusual electrochemical behaviour is attributed to a surface conversion reaction mechanism in contrast with the classic lithium intercalation reaction. Our findings will offer a potential new path in the design of positive electrode materials in lithium-ion batteries.

  6. Effect of electrode manufacturing defects on electrochemical performance of lithium-ion batteries: Cognizance of the battery failure sources

    Science.gov (United States)

    Mohanty, D.; Hockaday, E.; Li, J.; Hensley, D. K.; Daniel, C.; Wood, D. L.

    2016-04-01

    During LIB electrode manufacturing, it is difficult to avoid the certain defects that diminish LIB performance and shorten the life span of the batteries. This study provides a systematic investigation correlating the different plausible defects (agglomeration/blisters, pinholes/divots, metal particle contamination, and non-uniform coating) in a LiNi0.5Mn0.3Co0.2O2 positive electrode with its electrochemical performance. In addition, an infrared thermography technique was demonstrated as a nondestructive tool to detect these defects. The findings show that cathode agglomerates aggravated cycle efficiency, and resulted in faster capacity fading at high current density. Electrode pinholes showed substantially lower discharge capacities at higher current densities than baseline NMC 532electrodes. Metal particle contaminants have an extremely negative effect on performance, at higher C-rates. The electrodes with more coated and uncoated interfaces (non-uniform coatings) showed poor cycle life compared with electrodes with fewer coated and uncoated interfaces. Further, microstructural investigation provided evidence of presence of carbon-rich region in the agglomerated region and uneven electrode coating thickness in the coated and uncoated interfacial regions that may lead to the inferior electrochemical performance. This study provides the importance of monitoring and early detection of the electrode defects during LIB manufacturing processes to minimize the cell rejection rate after fabrication and testing.

  7. A highly permeable and enhanced surface area carbon-cloth electrode for vanadium redox flow batteries

    Science.gov (United States)

    Zhou, X. L.; Zhao, T. S.; Zeng, Y. K.; An, L.; Wei, L.

    2016-10-01

    In this work, a high-performance porous electrode, made of KOH-activated carbon-cloth, is developed for vanadium redox flow batteries (VRFBs). The macro-scale porous structure in the carbon cloth formed by weaving the carbon fibers in an ordered manner offers a low tortuosity (∼1.1) and a broad pore distribution from 5 μm to 100 μm, rendering the electrode a high hydraulic permeability and high effective ionic conductivity, which are beneficial for the electrolyte flow and ion transport through the porous electrode. The use of KOH activation method to create nano-scale pores on the carbon-fiber surfaces leads to a significant increase in the surface area for redox reactions from 2.39 m2 g-1 to 15.4 m2 g-1. The battery assembled with the present electrode delivers an energy efficiency of 80.1% and an electrolyte utilization of 74.6% at a current density of 400 mA cm-2, as opposed to an electrolyte utilization of 61.1% achieved by using a conventional carbon-paper electrode. Such a high performance is mainly attributed to the combination of the excellent mass/ion transport properties and the high surface area rendered by the present electrode. It is suggested that the KOH-activated carbon-cloth electrode is a promising candidate in redox flow batteries.

  8. Graphene Oxide-Based Electrode Inks for 3D-Printed Lithium-Ion Batteries.

    Science.gov (United States)

    Fu, Kun; Wang, Yibo; Yan, Chaoyi; Yao, Yonggang; Chen, Yanan; Dai, Jiaqi; Lacey, Steven; Wang, Yanbin; Wan, Jiayu; Li, Tian; Wang, Zhengyang; Xu, Yue; Hu, Liangbing

    2016-04-06

    All-component 3D-printed lithium-ion batteries are fabricated by printing graphene-oxide-based composite inks and solid-state gel polymer electrolyte. An entirely 3D-printed full cell features a high electrode mass loading of 18 mg cm(-2) , which is normalized to the overall area of the battery. This all-component printing can be extended to the fabrication of multidimensional/multiscale complex-structures of more energy-storage devices.

  9. Thick electrodes for Li-ion batteries: A model based analysis

    Science.gov (United States)

    Danner, Timo; Singh, Madhav; Hein, Simon; Kaiser, Jörg; Hahn, Horst; Latz, Arnulf

    2016-12-01

    Li-ion batteries are commonly used in portable electronic devices due to their outstanding energy and power density. A remaining issue which hinders the breakthrough e.g. in the automotive sector is the high production cost. For low power applications, such as stationary storage, batteries with electrodes thicker than 300 μm were suggested. High energy densities can be attained with only a few electrode layers which reduces production time and cost. However, mass and charge transport limitations can be severe at already small C-rates due to long transport pathways. In this article we use a detailed 3D micro-structure resolved model to investigate limiting factors for battery performance. The model is parametrized with data from the literature and dedicated experiments and shows good qualitative agreement with experimental discharge curves of thick NMC-graphite Li-ion batteries. The model is used to assess the effect of inhomogeneities in carbon black distribution and gives answers to the possible occurrence of lithium plating during battery charge. Based on our simulations we can predict optimal operation strategies and improved design concepts for future Li-ion batteries employing thick electrodes.

  10. XPS investigations of electrolyte/electrode interactions for various Li-ion battery materials

    Energy Technology Data Exchange (ETDEWEB)

    Oswald, S.; Mikhailova, D.; Scheiba, F.; Reichel, P.; Fiedler, A.; Ehrenberg, H. [IFW Dresden, Dresden (Germany)

    2011-05-15

    For future Li-ion battery applications the search for both new design concepts and materials is necessary. The electrodes of the batteries are always in contact with electrolytes, which are responsible for the transport of Li ions during the charging and discharging process. A broad range of materials is considered for both electrolytes and electrodes so that very different chemical interactions between them can occur, while good cycling behavior can only be obtained for stable solid-electrolyte interfaces. X-ray photoelectron spectroscopy (XPS) was used to study the most relevant interactions between various electrode materials in contact with different electrolyte solutions. It is shown how XPS can provide useful information on reactivities and thus preselect suitable electrode/electrolyte combinations, prior to electrochemical performance tests. (orig.)

  11. Studies on the oxygen reduction catalyst for zinc-air battery electrode

    Science.gov (United States)

    Wang, Xianyou; Sebastian, P. J.; Smit, Mascha A.; Yang, Hongping; Gamboa, S. A.

    In this paper, perovskite type La 0.6Ca 0.4CoO 3 as a catalyst of oxygen reduction was prepared, and the structure and performance of the catalysts was examined by means of IR, X-ray diffraction (XRD), and thermogravimetric (TG). Mixed catalysts doped, some metal oxides were put also used. The cathodic polarization curves for oxygen reduction on various catalytic electrodes were measured by linear sweep voltammetry (LSV). A Zn-air battery was made with various catalysts for oxygen reduction, and the performance of the battery was measured with a BS-9300SM rechargeable battery charge/discharge device. The results showed that the perovskite type catalyst (La 0.6Ca 0.4CoO 3) doped with metal oxide is an excellent catalyst for the zinc-air battery, and can effectively stimulate the reduction of oxygen and improve the properties of zinc-air batteries, such as discharge capacity, etc.

  12. Reversible and irreversible dilation of lithium-ion battery electrodes investigated by in-situ dilatometry

    Science.gov (United States)

    Sauerteig, Daniel; Ivanov, Svetlozar; Reinshagen, Holger; Bund, Andreas

    2017-02-01

    The technique of electrochemical in-situ dilatometry is applied to study the intercalation induced macroscopic expansion of electrodes for lithium-ion batteries. A full cell setup is used to investigate the expansion under real conditions. This method enables in-situ measurement of expansion under defined pressure, using conventional electrodes, separators and electrolytes. To understand the influence of the microstructure, the swelling behavior of different LiNi1/3 Mn1/3 Co1/3 O2 (NMC) positive electrodes and graphite negative electrodes is measured and systematically analyzed. A theoretical approach for assessment of reversible electrode displacement in a full cell is developed, by using a low number of material specific input parameters. Electrochemical in-situ dilatometry is able to show differences in irreversible dilation depending on electrode design and therefore it is a powerful technique for stability and lifetime assessment.

  13. Oriented nanotube electrodes for lithium ion batteries and supercapacitors

    Science.gov (United States)

    Frank, Arthur J.; Zhu, Kai; Wang, Qing

    2013-03-05

    An electrode having an oriented array of multiple nanotubes is disclosed. Individual nanotubes have a lengthwise inner pore defined by interior tube walls which extends at least partially through the length of the nanotube. The nanotubes of the array may be oriented according to any identifiable pattern. Also disclosed is a device featuring an electrode and methods of fabrication.

  14. A method for making nickel electrodes for alkaline storage batteries

    Energy Technology Data Exchange (ETDEWEB)

    Okhira, T.; Inaba, K.; Kumano, Y.; Yamaga, M.

    1983-07-14

    A nitrate or chloride of ruthenium is added to an aqueous NiNO3 solution and then a porous plate is submerged into it, which serves as the electrode base. Electrolysis is then performed using the plate as the cathode. The electrode is caked. It has excellent electrical characteristics.

  15. Infiltrated Porous Polymer Sheets as Free-Standing Flexible Lithium-Sulfur Battery Electrodes.

    Science.gov (United States)

    Wu, Feixiang; Zhao, Enbo; Gordon, Daniel; Xiao, Yiran; Hu, Chenchen; Yushin, Gleb

    2016-08-01

    Free-standing, high-capacity Li2 S electrodes with capacity loadings in the range from 1.5 to 3.8 mA h cm(-2) are produced by using infiltration of active materials into porous carbonized biomass sheets. The proposed electrode design can be effectively utilized for the low-cost fabrication of flexible lithium batteries with high specific energy.

  16. Electrochemical impedance characterization of FeSn{sub 2} electrodes for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chamas, M.; Lippens, P-E.; Jumas, J-C. [Institut Charles Gerhardt, Equipe Agregats Interfaces et Materiaux pour l' Energie, UMR 5253 CNRS, Universite Montpellier 2, Place Eugene Bataillon, 34095 Montpellier cedex 5 (France); Hassoun, J., E-mail: jusef.hassoun@uniroma1.it [Dipartemento di Chimica, Universita di Roma, ' La Sapienza' , 00185 Rome (Italy); Panero, S.; Scrosati, B. [Dipartemento di Chimica, Universita di Roma, ' La Sapienza' , 00185 Rome (Italy)

    2011-07-30

    Highlights: > In this paper we study a tin based, FeSn{sub 2}, high capacity lithium-alloying electrode. > The electrochemical performance of this electrode in lithium batteries is remarkably influenced by the current rate. > This aspect is investigated by electrochemical techniques such as galvanostatic cycling and impedance spectroscopy. > The results demonstrated that the good electrochemical behavior of the electrode at the higher currents is due to the formation of a stable solid electrolyte interphase (SEI) film. - Abstract: This work reports the electrochemical characterization of a micro-scale FeSn{sub 2} electrode in a lithium battery. The electrode is proposed as anode material for advanced lithium ion batteries due to its characteristics of high capacity (500 mAh g{sup -1}) and low working voltage (0.6 V vs. Li). The electrochemical alloying process is studied by cyclic voltammetry and galvanostatic cycling while the interfacial properties are investigated by electrochemical impedance spectroscopy. The impedance measurements in combination with the galvanostatic cycling tests reveal relatively low overall impedance values and good electrochemical performance for the electrode, both in terms of delivered capacity and cycling stability, even at the higher C-rate regimes.

  17. The Influence of Electrode and Channel Configurations on Flow Battery Performance

    Energy Technology Data Exchange (ETDEWEB)

    Darling, RM; Perry, ML

    2014-05-21

    Flow batteries with flow-through porous electrodes are compared to cells with porous electrodes adjacent to either parallel or interdigitated channels. Resistances and pressure drops are measured for different configurations to augment the electrochemical data. Cell tests are done with an electrolyte containing VO2+ and VO2+ in sulfuric acid that is circulated through both anode and cathode from a single reservoir. Performance is found to depend sensitively on the combination of electrode and flow field. Theoretical explanations for this dependence are provided. Scale-up of flow through and interdigitated designs to large active areas is also discussed. (C) 2014 The Electrochemical Society. All rights reserved.

  18. Performance characteristics of lead oxides in pasted lead/acid battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Afifi, S.E. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt)); Saba, A.E. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt)); Shenouda, A.Y. (Electrometallurgy Lab., Central Metallurgical Research and Development Inst., Cairo (Egypt))

    1993-10-15

    The performance characteristics of lead oxides used for the pasted type of lead/acid battery plate have been investigated. The [alpha]- and [beta]-PbO polymorphs have been prepared carefully and used for pasting model electrodes. The factors that may affect the electrical capacity of such electrodes have been studied. These are: the type of oxide; percentage of free lead; additives such as carboxymethyl cellulose, zeolite and graphite. Lead hydroxide has also been studied with special attention. Photomicrographs have been taken to examine the crystal forms that develop on the electrode surface. Finally, some industrial samples have been investigated. (orig.)

  19. Spinel electrodes from the Li-Mn-O system for rechargeable lithium battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Thackeray, M.M.; de Kock, A.; Rossouw, M.H.; Liles, D. (Div. of Materials Science and Technology, CSIR, Pretoria 0001 (ZA)); Bittihn, R.; Hoge, D. (VARTA Batterie AG Research Center, D-6233 Kelkheim (DE))

    1992-02-01

    The electrochemical and structural properties of spinel phases in the Li-Mn-O system are discussed as insertion electrodes for rechargeable lithium batteries. In this paper the performance of button-type cells containing electrodes from the Li{sub 2}O yMnO{sub 2} system, e.g., the stoichiometric spinel Li{sub 4}Mn{sup 5}O{sub 12}(y = 2.5) and the defect spinel Li{sub 2}Mn{sub 4}O{sub 9}(y = 4.0), is highlighted and compared with a cell containing a standard LiMn{sub 2}O{sub 4} spinel electrode.

  20. High rate capability pure Sn-based nano-architectured electrode assembly for rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Bazin, L.; Mitra, S.; Taberna, P.L.; Gressier, M.; Menu, M.J.; Barnabe, A.; Simon, P. [CIRIMAT-UMR 5085- Universite Paul Sabatier, route de Narbonne, 31062 Toulouse Cedex 4 (France); Poizot, P.; Tarascon, J.-M. [LRCS-UMR 6007-Universite de Picardie Jules Verne, 33 rue Saint-Leu, 80039 Amiens (France)

    2009-03-15

    New high surface area nano-architectured copper current collectors have been designed based on simple electrodeposition method. The nano-architectured electrode design not only increases the effective surface area of the electrode but it is also very suitable for sustaining the mechanical and structural strain during electrochemical reaction. In this work, a nano-architectured Sn anode for Li-ion battery, based on Li-Sn alloying reaction, delivers very high cycle life and good power performance compared to planar tin films. This electrode could be successfully used in the field of 3D microbatteries. (author)

  1. Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries using Synchrotron Radiation Techniques

    Energy Technology Data Exchange (ETDEWEB)

    Mehta, Apurva; Stanford Synchrotron Radiation Lightsource; Doeff, Marca M.; Chen, Guoying; Cabana, Jordi; Richardson, Thomas J.; Mehta, Apurva; Shirpour, Mona; Duncan, Hugues; Kim, Chunjoong; Kam, Kinson C.; Conry, Thomas

    2013-04-30

    We describe the use of synchrotron X-ray absorption spectroscopy (XAS) and X-ray diffraction (XRD) techniques to probe details of intercalation/deintercalation processes in electrode materials for Li ion and Na ion batteries. Both in situ and ex situ experiments are used to understand structural behavior relevant to the operation of devices.

  2. High surface area carbon for bifunctional air electrodes applied in zinc-air batteries

    Energy Technology Data Exchange (ETDEWEB)

    Arai, H. [on leave from NTT Laboratories (Japan); Mueller, S.; Haas, O. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    Bifunctional air electrodes with high surface area carbon substrates showed low reduction overpotential, thus are promising for enhancing the energy efficiency and power capability of zinc-air batteries. The improved performance is attributed to lower overpotential due to diffusion of the reaction intermediate, namely the peroxide ion. (author) 1 fig., 2 refs.

  3. Impedance Simulation of a Li-Ion Battery with Porous Electrodes and Spherical Li+ Intercalation Particles

    NARCIS (Netherlands)

    Huang, R.W.J.M.; Chung, F.; Kelder, E.M.

    2006-01-01

    We present a semimathematical model for the simulation of the impedance spectra of a rechargeable lithium batteries consisting of porous electrodes with spherical Li+ intercalation particles. The particles are considered to have two distinct homogeneous phases as a result of the intercalation and de

  4. Geometric Characteristics of Three Dimensional Reconstructed Anode Electrodes of Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Cheolwoong Lim

    2014-04-01

    Full Text Available The realistic three dimensional (3D microstructure of lithium ion battery (LIB electrode plays a key role in studying the effects of inhomogeneous microstructures on the performance of LIBs. However, the complexity of realistic microstructures imposes a significant computational cost on numerical simulation of large size samples. In this work, we used tomographic data obtained for a commercial LIB graphite electrode to evaluate the geometric characteristics of the reconstructed electrode microstructure. Based on the analysis of geometric properties, such as porosity, specific surface area, tortuosity, and pore size distribution, a representative volume element (RVE that retains the geometric characteristics of the electrode material was obtained for further numerical studies. In this work, X-ray micro-computed tomography (CT with 0.56 μm resolution was employed to capture the inhomogeneous porous microstructures of LIB anode electrodes. The Sigmoid transform function was employed to convert the initial raw tomographic images to binary images. Moreover, geometric characteristics of an anode electrode after 2400 cycles at the charge/discharge rate of 1 C were compared with those of a new anode electrode to investigate morphological change of the electrode. In general, the cycled electrode shows larger porosity, smaller tortuosity, and similar specific surface area compared to the new electrode.

  5. Electrochemical behavior of LiCoO2 as aqueous lithium-ion battery electrodes

    KAUST Repository

    Ruffo, Riccardo

    2009-02-01

    Despite the large number of studies on the behavior of LiCoO2 in organic electrolytes and its recent application as a positive electrode in rechargeable water battery prototypes, a little information is available about the lithium intercalation reaction in this layered compound in aqueous electrolytes. This work shows that LiCoO2 electrodes can be reversibly cycled in LiNO3 aqueous electrolytes for tens of cycles at remarkably high rates with impressive values specific capacity higher than 100 mAh/g, and with a coulomb efficiency greater than 99.7%. Stable and reproducible cycling measurements have been made using a simple cell design that can be easily applied to the study of other intercalation materials, assuming that they are stable in water and that their intercalation potential range matches the electrochemical stability window of the aqueous electrolyte. The experimental arrangement uses a three-electrode flooded cell in which another insertion compound acts as a reversible source and sink of lithium ions, i.e., as the counter electrode. A commercial reference electrode is also present. Both the working and the counter electrodes have been prepared as thin layers on a metallic substrate using the procedures typical for the study of electrodes for lithium-ion batteries in organic solvent electrolytes. © 2008 Elsevier B.V. All rights reserved.

  6. Solvent-Free Manufacturing of Electrodes for Lithium-ion Batteries

    Science.gov (United States)

    Ludwig, Brandon; Zheng, Zhangfeng; Shou, Wan; Wang, Yan; Pan, Heng

    2016-03-01

    Lithium ion battery electrodes were manufactured using a new, completely dry powder painting process. The solvents used for conventional slurry-cast electrodes have been completely removed. Thermal activation time has been greatly reduced due to the time and resource demanding solvent evaporation process needed with slurry-cast electrode manufacturing being replaced by a hot rolling process. It has been found that thermal activation time to induce mechanical bonding of the thermoplastic polymer to the remaining active electrode particles is only a few seconds. Removing the solvent and drying process allows large-scale Li-ion battery production to be more economically viable in markets such as automotive energy storage systems. By understanding the surface energies of various powders which govern the powder mixing and binder distribution, bonding tests of the dry-deposited particles onto the current collector show that the bonding strength is greater than slurry-cast electrodes, 148.8 kPa as compared to 84.3 kPa. Electrochemical tests show that the new electrodes outperform conventional slurry processed electrodes, which is due to different binder distribution.

  7. Failure mechanisms of single-crystal silicon electrodes in lithium-ion batteries

    Science.gov (United States)

    Shi, Feifei; Song, Zhichao; Ross, Philip N.; Somorjai, Gabor A.; Ritchie, Robert O.; Komvopoulos, Kyriakos

    2016-06-01

    Long-term durability is a major obstacle limiting the widespread use of lithium-ion batteries in heavy-duty applications and others demanding extended lifetime. As one of the root causes of the degradation of battery performance, the electrode failure mechanisms are still unknown. In this paper, we reveal the fundamental fracture mechanisms of single-crystal silicon electrodes over extended lithiation/delithiation cycles, using electrochemical testing, microstructure characterization, fracture mechanics and finite element analysis. Anisotropic lithium invasion causes crack initiation perpendicular to the electrode surface, followed by growth through the electrode thickness. The low fracture energy of the lithiated/unlithiated silicon interface provides a weak microstructural path for crack deflection, accounting for the crack patterns and delamination observed after repeated cycling. On the basis of this physical understanding, we demonstrate how electrolyte additives can heal electrode cracks and provide strategies to enhance the fracture resistance in future lithium-ion batteries from surface chemical, electrochemical and material science perspectives.

  8. The Science of Electrode Materials for Lithium Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fultz, Brent

    2007-03-15

    Rechargeable lithium batteries continue to play the central role in power systems for portable electronics, and could play a role of increasing importance for hybrid transportation systems that use either hydrogen or fossil fuels. For example, fuel cells provide a steady supply of power, whereas batteries are superior when bursts of power are needed. The National Research Council recently concluded that for dismounted soldiers "Among all possible energy sources, hybrid systems provide the most versatile solutions for meeting the diverse needs of the Future Force Warrior. The key advantage of hybrid systems is their ability to provide power over varying levels of energy use, by combining two power sources." The relative capacities of batteries versus fuel cells in a hybrid power system will depend on the capabilities of both. In the longer term, improvements in the cost and safety of lithium batteries should lead to a substantial role for electrochemical energy storage subsystems as components in fuel cell or hybrid vehicles. We have completed a basic research program for DOE BES on anode and cathode materials for lithium batteries, extending over 6 years with a 1 year phaseout period. The emphasis was on the thermodynamics and kinetics of the lithiation reaction, and how these pertain to basic electrochemical properties that we measure experimentally — voltage and capacity in particular. In the course of this work we also studied the kinetic processes of capacity fade after cycling, with unusual results for nanostructued Si and Ge materials, and the dynamics underlying electronic and ionic transport in LiFePO4. This document is the final report for this work.

  9. Multilayered Electride Ca2N Electrode via Compression Molding Fabrication for Sodium Ion Batteries.

    Science.gov (United States)

    Chen, Guanghai; Bai, Ying; Li, Hui; Li, Yu; Wang, Zhaohua; Ni, Qiao; Liu, Lu; Wu, Feng; Yao, Yugui; Wu, Chuan

    2017-03-01

    Pursuing for novel electrode materials is significant for the progress of sodium ion batteries (SIBs). Here, a multilayered electride prepared by simple thermal decomposition of solid Ca3N2, namely Ca2N, is introduced as a new anode material of SIBs for the first time, and a compression molding electrode fabricated by pressing Ca2N powder into nickel foam is applied to protect Ca2N from trace moisture and oxygen. The as-prepared electrode delivers an initial discharge capacity of 1110.5 mAh g(-1) and a reversible discharge capacity of ∼320 mAh g(-1). These results suggest that Ca2N has a great potential for sodium ion batteries.

  10. Effects of Nanoparticle Geometry and Size Distribution on Diffusion Impedance of Battery Electrodes

    CERN Document Server

    Song, J

    2012-01-01

    The short diffusion lengths in insertion battery nanoparticles render the capacitive behavior of bounded diffusion, which is rarely observable with conventional larger particles, now accessible to impedance measurements. Coupled with improved geometrical characterization, this presents an opportunity to measure solid diffusion more accurately than the traditional approach of fitting Warburg circuit elements, by properly taking into account the particle geometry and size distribution. We revisit bounded diffusion impedance models and incorporate them into an overall impedance model for different electrode configurations. The theoretical models are then applied to experimental data of a silicon nanowire electrode to show the effects of including the actual nanowire geometry and radius distribution in interpreting the impedance data. From these results, we show that it is essential to account for the particle shape and size distribution to correctly interpret impedance data for battery electrodes. Conversely, it...

  11. LDHs as electrode materials for electrochemical detection and energy storage: supercapacitor, battery and (bio)-sensor.

    Science.gov (United States)

    Mousty, Christine; Leroux, Fabrice

    2012-11-01

    From an exhaustive overview based on applicative academic literature and patent domain, the relevance of Layered Double Hydroxide (LDHs) as electrode materials for electrochemical detection of organic molecules having environmental or health impact and energy storage is evaluated. Specifically the focus is driven on their application as supercapacitor, alkaline or lithium battery and (bio)-sensor. Inherent to the high versatility of their chemical composition, charge density, anion exchange capability, LDH-based materials are extensively studied and their performances for such applications are reported. Indeed the analytical characteristics (sensitivity and detection limit) of LDH-based electrodes are scrutinized, and their specific capacity or capacitance as electrode battery or supercapacitor materials, are detailed.

  12. Electrochemical Investigation of Carbon as Additive to the Negative Electrode of Lead-Acid Battery

    Directory of Open Access Journals (Sweden)

    Fernandez Matthew M.

    2015-01-01

    Full Text Available The increasing demand of cycle life performance of Pb-acid batteries requires the improvement of the negative Pb electrode’s charge capacity. Electrochemical investigations were performed on Pb electrode and Pb+Carbon (Carbon black and Graphite electrodes to evaluate the ability of the additives to enhance the electrochemical faradaic reactions that occur during the cycle of Pb-acid battery negative electrode. The electrodes were characterized through Cyclic Voltammetry (CV, Potentiodynamic Polarization (PP, and Electrochemical Impedance Spectroscopy (EIS. CV revealed that the addition of carbon on the Pb electrode increased anodic and cathodicreactions by tenfold. The kinetics of PbSO4 passivation measured through PPrevealed that the addition of Carbon on the Pb electrode accelerated the oxide formation by tenfold magnitude. The Nyquist plot measured through EIS suggest that the electrochemical mechanism and reaction kinetics is under charge-transfer. From the equivalent circuit and physical model, Pb+CB1 electrode has the lowest EIS parameters while Pb+G has the highest which is attributed to faster faradaic reaction.The Nyquist plot of the passivated Pb+CB1 electrode showed double semicircular shape. The first layer represents to the bulk passive PbSO4 layer and the second layer represents the Carbon+PbSO4 layer. The enhancements upon addition of carbon on the Pb electrode were attributed to the additive’s electrical conductivity and total surface area. The electrochemical active sites for the PbSO4 to nucleate and spread increases upon addition of electrical conductive and high surface area carbon additives.

  13. Quantitative Analysis of Three-dimensional Microstructure of Li-ion Battery Electrodes

    Science.gov (United States)

    Liu, Zhao

    Li-ion batteries (LIBs) have attracted considerable attention in the past two decades due to their widespread applications in portable electronics, and their growing use in electric vehicles and large-scale grid storage. Increasing battery energy density and powder density while maintaining long life, along with battery safety, are the biggest challenges that limit their further development. Various approaches with materials and chemistry have been employed to improve performance. However, one less-studied aspect that also impacts performance is the electrode microstructure. In particular, three-dimensional (3D) electrode microstructural data for LIB electrodes, which were not widely available prior to this thesis, can provide important input for understanding and improving LIB performance. The focus of this thesis is to apply 3D tomographic techniques, together with electrochemical performance data, to obtain LIB microstructure-performance correlations. Two advanced 3D structural analysis techniques, focused ion beam-scanning electron microscopy (FIB-SEM) and transmission X-ray microscopy (TXM) nanotomography, are used to quantify LIB electrode microstructure. 3D characterization of LIB electrode microstructure is used to obtain a deeper understanding of mechanisms that limit LIB performance. Microstructural characterization before and after cycling is used to explore capacity loss mechanisms. It is hoped that the results can guide electrode microstructures design to improve performance and stability. Two types of commercial electrodes, LiCoO2 and LiCoO 2/Li(Ni1/3Mn1/3Co1/3)O2, are studied using FIB-SEM and TXM. Both methods were found to be applicable to quantifying the oxide particle microstructure, including volume fraction, surface area, and particle size distribution, and results agreed well. However, structural inhomogeneity found in these commercial samples, limited the capability to resolve microstructural changes during cycling. In order to also quantify

  14. A flexible Li-ion battery with design towards electrodes electrical insulation

    Science.gov (United States)

    Vieira, E. M. F.; Ribeiro, J. F.; Sousa, R.; Correia, J. H.; Goncalves, L. M.

    2016-08-01

    The application of micro electromechanical systems (MEMS) technology in several consumer electronics leads to the development of micro/nano power sources with high power and MEMS integration possibility. This work presents the fabrication of a flexible solid-state Li-ion battery (LIB) (~2.1 μm thick) with a design towards electrodes electrical insulation, using conventional, low cost and compatible MEMS fabrication processes. Kapton® substrate provides flexibility to the battery. E-beam deposited 300 nm thick Ge anode was coupled with LiCoO2/LiPON (cathode/solid-state electrolyte) in a battery system. LiCoO2 and LiPON films were deposited by RF-sputtering with a power source of 120 W and 100 W, respectively. LiCoO2 film was annealed at 400 °C after deposition. The new design includes Si3N4 and LiPO thin-films, providing electrode electrical insulation and a battery chemical stability safeguard, respectively. Microstructure and battery performance were investigated by scanning electron microscopy, electric resistivity and electrochemical measurements (open circuit potential, charge/discharge cycles and electrochemical impedance spectroscopy). A rechargeable thin-film and lightweight flexible LIB using MEMS processing compatible materials and techniques is reported.

  15. Multiscale simulation process and application to additives in porous composite battery electrodes

    Science.gov (United States)

    Wieser, Christian; Prill, Torben; Schladitz, Katja

    2015-03-01

    Structure-resolving simulation of porous materials in electrochemical cells such as fuel cells and lithium ion batteries allows for correlating electrical performance with material morphology. In lithium ion batteries characteristic length scales of active material particles and additives range several orders of magnitude. Hence, providing a computational mesh resolving all length scales is not reasonably feasible and requires alternative approaches. In the work presented here a virtual process to simulate lithium ion batteries by bridging the scales is introduced. Representative lithium ion battery electrode coatings comprised of μm-scale graphite particles as active material and a nm-scale carbon/polymeric binder mixture as an additive are imaged with synchrotron radiation computed tomography (SR-CT) and sequential focused ion beam/scanning electron microscopy (FIB/SEM), respectively. Applying novel image processing methodologies for the FIB/SEM images, data sets are binarized to provide a computational grid for calculating the effective mass transport properties of the electrolyte phase in the nanoporous additive. Afterwards, the homogenized additive is virtually added to the micropores of the binarized SR-CT data set representing the active particle structure, and the resulting electrode structure is assembled to a virtual half-cell for electrochemical microheterogeneous simulation. Preliminary battery performance simulations indicate non-negligible impact of the consideration of the additive.

  16. Design of Hydrogen Storage Alloys/Nanoporous Metals Hybrid Electrodes for Nickel-Metal Hydride Batteries

    Science.gov (United States)

    Li, M. M.; Yang, C. C.; Wang, C. C.; Wen, Z.; Zhu, Y. F.; Zhao, M.; Li, J. C.; Zheng, W. T.; Lian, J. S.; Jiang, Q.

    2016-06-01

    Nickel metal hydride (Ni-MH) batteries have demonstrated key technology advantages for applications in new-energy vehicles, which play an important role in reducing greenhouse gas emissions and the world’s dependence on fossil fuels. However, the poor high-rate dischargeability of the negative electrode materials—hydrogen storage alloys (HSAs) limits applications of Ni-MH batteries in high-power fields due to large polarization. Here we design a hybrid electrode by integrating HSAs with a current collector of three-dimensional bicontinuous nanoporous Ni. The electrode shows enhanced high-rate dischargeability with the capacity retention rate reaching 44.6% at a discharge current density of 3000 mA g‑1, which is 2.4 times that of bare HSAs (18.8%). Such a unique hybrid architecture not only enhances charge transfer between nanoporous Ni and HSAs, but also facilitates rapid diffusion of hydrogen atoms in HSAs. The developed HSAs/nanoporous metals hybrid structures exhibit great potential to be candidates as electrodes in high-performance Ni-MH batteries towards applications in new-energy vehicles.

  17. Vanadium based amorphous mixed oxides used as negative electrodes of lithium batteries; Oxydes mixtes amorphes a base de vanadium comme electrodes negatives de batteries au lithium

    Energy Technology Data Exchange (ETDEWEB)

    Guyomard, D.; Leroux, F.; Sigala, C.; Le Gal La Salle, A.; Piffard, Y. [Institut des Materiaux de Nantes, 44 (France). Laboratoire de Chimie des Solides

    1996-12-31

    This paper presents recent results concerning the chemical and electrochemical synthesis, the electrochemical properties and the characterization of two new families of amorphous oxides of formula Li{sub x}MVO{sub 4} (1electrodes in high performance lithium-ion batteries. (J.S.) 19 refs.

  18. Novel configuration of bifunctional air electrodes for rechargeable zinc-air batteries

    Science.gov (United States)

    Li, Po-Chieh; Chien, Yu-Ju; Hu, Chi-Chang

    2016-05-01

    A novel configuration of two electrodes containing electrocatalysts for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) pressed into a bifunctional air electrode is designed for rechargeable Zn-air batteries. MOC/25BC carbon paper (MOC consisting of α-MnO2 and XC-72 carbon black) and Fe0.1Ni0.9Co2O4/Ti mesh on this air electrode mainly serve as the cathode for the ORR and the anode for the OER, respectively. The morphology and physicochemical properties of Fe0.1Ni0.9Co2O4 are investigated through scanning electron microscopy, inductively coupled plasma-mass spectrometry, and X-ray diffraction. Electrochemical studies comprise linear sweep voltammetry, rotating ring-disk electrode voltammetry, and the full-cell charge-discharge-cycling test. The discharge peak power density of the Zn-air battery with the unique air electrode reaches 88.8 mW cm-2 at 133.6 mA cm-2 and 0.66 V in an alkaline electrolyte under an ambient atmosphere. After 100 charge-discharge cycles at 10 mA cm-2, an increase of 0.3 V between charge and discharge cell voltages is observed. The deep charge-discharge curve (10 h in each step) indicates that the cell voltages of discharge (1.3 V) and charge (1.97 V) remain constant throughout the process. The performance of the proposed rechargeable Zn-air battery is superior to that of most other similar batteries reported in recent studies.

  19. Modelling of cycling of lithium battery with microporous carbon electrode

    Directory of Open Access Journals (Sweden)

    D. Portnyagin

    2008-12-01

    Full Text Available Charge/discharge cycles of lithium cell with microporous carbon electrode under potentiodynamic control have been modelled. Predictions of the models with variable and constant diffusion coefficient neglecting the electric field inside the particle (CPM, DFM are compared to the predictions of the models with variable and constant diffusion coefficient in which electrostatic interaction inside the particles of carbon electrode (CPME, DFME is taken into account. There is observed a considerable difference between both. Electrostatic interactions of lithium ions with each other and the charge distributed inside the particle promote intercalation during the discharge of the cell and deintercalation during the charge. The dependance of the effect of hysteresis during the cycling of the cell on the rate of change of the applied voltage is studied. The larger is the speed of change of the applied voltage the more effective is hysteresis. We have also obtained concentration profiles at different stages of charge/discharge process.

  20. Towards ultrathick battery electrodes: aligned carbon nanotube-enabled architecture.

    Science.gov (United States)

    Evanoff, Kara; Khan, Javed; Balandin, Alexander A; Magasinski, Alexandre; Ready, W Jud; Fuller, Thomas F; Yushin, Gleb

    2012-01-24

    Vapor deposition techniques were utilized to synthesize very thick (∼1 mm) Li-ion battery anodes consisting of vertically aligned carbon nanotubes coated with silicon and carbon. The produced anode demonstrated ultrahigh thermal (>400 W·m(-1) ·K(-1)) and high electrical (>20 S·m(-1)) conductivities, high cycle stability, and high average capacity (>3000 mAh·g(Si) (-1)). The processes utilized allow for the conformal deposition of other materials, thus making it a promising architecture for the development of Li-ion anodes and cathodes with greatly enhanced electrical and thermal conductivities.

  1. A method for making electrodes for an alkaline storage battery

    Energy Technology Data Exchange (ETDEWEB)

    Isikava, T.; Ivaki, T.; Matsumoto, I.; Yanagikhara, N.

    1983-02-16

    The surface of a porous of a foam metal plate filled with an active mass is covered by a mixture of a fiberous material with an electrolyte resistant powder of a thermoplastic resin. Heating the plate to a temperature close to the melting point of the resin, the powder and fiberous material is melted. Fibers of polyacrylnitrile or carbon and polyethylene powder are used. The produced electrode has a long service life.

  2. Kinetic characteristics of mixed conductive electrodes for lithium ion batteries

    Science.gov (United States)

    Ma, Jianxin; Wang, Chunsheng; Wroblewski, Shannon

    The rate performances of four mixed conductive electrodes (Li 4/3Ti 5/3O 4, LiFePO 4, LiCoO 2 and LiCo 1/3Ni 1/3Mn 1/3O 2) were investigated using galvanostatic charge/discharge, electrochemical impedance Spectroscopy (EIS) and galvanostatic intermittent titration (GITT). These four electrode materials can be roughly divided into two groups according to the structure change during Li intercalation/extraction, i.e. the phase transition materials (Li 4/3Ti 5/3O 4 and LiFePO 4) and mixed phase transformation and solid solution materials (LiNi 1/3Mn 1/3Co 1/3O 2 and LiCoO 2). Both the ionic conductivity and phase transition kinetics have a strong impact on the rate capability of the electrode material in addition to the generally accepted factors such as particle size and electronic conductivity. The rate capabilities of Li 4/3Ti 5/3O 4 and LiFePO 4, which have an extended flat region in the charge/discharge curves, mainly depended on their phase transition kinetics. The rate performance of the solid solution materials were controlled by the ionic conductivity, with some influence from the electronic conductivity.

  3. Characteristics of graphite felt electrode electrochemically oxidized for vanadium redox battery application

    Institute of Scientific and Technical Information of China (English)

    LI Xiao-gang; HUANG Ke-long; LIU Su-qin; TAN Ning; CHEN Li-quan

    2007-01-01

    The graphite felt was oxidized at a positive electrode potential in sulfuric acid solution. The electrochemical performance of the treated graphite felt served as electrode for vanadium redox battery was investigated with FT-IR, SEM, XPS, BET, cyclic voltammetry and testing VRB system, respectively. The results show that the molar ratio of O to C increases from 0.085 to 0.15 due to the increase of -COOH functional groups during electrochemical oxidation treatment, and the GF surface is eroded by electrochemical oxidation, resulting in the surface area increase from 0.33 m2/g to 0.49 m2/g. The VRB with modified GF electrode exhibits excellent performance under a current density of 30 mA/cm2. The average current efficiency reaches 94% and average voltage efficiency reaches 85%. The improvement of electrochemical activity for the electrode is ascribed to the increase of the number of -COOH group and the special surface of GF.

  4. Polyacrylate bound TiSb2 electrodes for Li-ion batteries

    Science.gov (United States)

    Gómez-Cámer, Juan Luis; Novák, Petr

    2015-01-01

    Crystalline TiSb2 electrodes prepared using two different binders, PVDF and lithium polyacrylate (LiPAA), were examined as negative electrodes in Li-ion batteries. The cycle life of the electrodes is strongly influenced by the choice of the binder, reaching ca. 120 cycles with LiPAA vs. ca. 90 cycles achieved with the common binder PVDF. Moreover, rate capability is improved using LiPAA binder. The reduction in TiSb2 particle size is shown to influence the average practical specific charge at high charge/discharge rates. The reasons for this improvement are discussed and the optimized electrode was demonstrated in full Li-ion cells.

  5. Aging in chemically prepared divalent silver oxide electrodes for silver/zinc reserve batteries

    Science.gov (United States)

    Smith, David F.; Brown, Curtis

    The instability of silver(II) oxide electrodes used in silver/zinc reserve batteries is the well known cause of capacity loss and delayed activation in reserve batteries after they are stored in the dry, unactivated state for extended periods of time. Metal contaminants in sintered/electroformed electrodes destabilize the oxide and the solid state reaction between AgO and elemental silver results in the formation of the lower capacity monovalent oxide Ag 2O. Chemically prepared (CP) AgO can be used to avoid the metal contaminants and to minimize the interfacial contact area between AgO and Ag, thus minimizing the affects of aging on the electrodes. Electrodes were fabricated with CP AgO and polytetrafluoroethylene (PTFE) binder and expanded silver metal current collectors. Experimentally, both electrode active material compacts (AgO and binder only) and electrodes complete with AgO/binder and silver current collector were tested to evaluate the influence of the current collector on aging. The electrode samples were discharged at a constant rate of 50 mA cm -2 before and after storage at 60°C for 21 days as well as after storage at room ambient temperature conditions for 91 months. The results indicate that the affects of aging upon the AgO/binder compacts are insignificant for long term storage at room temperature. However, thermally accelerated aging at high temperature (60°C) affects both transient and stabilized load voltage as well as capacity. In terms of capacity, the AgO/binder mix itself looses about 5% capacity after 21 days dry storage at 60°C while electrodes complete with current collector loose about 8%. The 60% increase in capacity loss is attributed to the solid state reaction between AgO and elemental silver.

  6. Silicon oxycarbide glass-graphene composite paper electrode for long-cycle lithium-ion batteries

    Science.gov (United States)

    David, Lamuel; Bhandavat, Romil; Barrera, Uriel; Singh, Gurpreet

    2016-03-01

    Silicon and graphene are promising anode materials for lithium-ion batteries because of their high theoretical capacity; however, low volumetric energy density, poor efficiency and instability in high loading electrodes limit their practical application. Here we report a large area (approximately 15 cm × 2.5 cm) self-standing anode material consisting of molecular precursor-derived silicon oxycarbide glass particles embedded in a chemically-modified reduced graphene oxide matrix. The porous reduced graphene oxide matrix serves as an effective electron conductor and current collector with a stable mechanical structure, and the amorphous silicon oxycarbide particles cycle lithium-ions with high Coulombic efficiency. The paper electrode (mass loading of 2 mg cm-2) delivers a charge capacity of ~588 mAh g-1electrode (~393 mAh cm-3electrode) at 1,020th cycle and shows no evidence of mechanical failure. Elimination of inactive ingredients such as metal current collector and polymeric binder reduces the total electrode weight and may provide the means to produce efficient lightweight batteries.

  7. Conformal coating of thin polymer electrolyte layer on nanostructured electrode materials for three-dimensional battery applications.

    Science.gov (United States)

    Gowda, Sanketh R; Reddy, Arava Leela Mohana; Shaijumon, Manikoth M; Zhan, Xiaobo; Ci, Lijie; Ajayan, Pulickel M

    2011-01-12

    Various three-dimensional (3D) battery architectures have been proposed to address effective power delivery in micro/nanoscale devices and for increasing the stored energy per electrode footprint area. One step toward obtaining 3D configurations in batteries is the formation of core-shell nanowires that combines electrode and electrolyte materials. One of the major challenges however in creating such architectures has been the coating of conformal thin nanolayers of polymer electrolytes around nanostructured electrodes. Here we show conformal coatings of 25-30 nm poly(methyl methacralate) electrolyte layers around individual Ni-Sn nanowires used as anodes for Li ion battery. This configuration shows high discharge capacity and excellent capacity retention even at high rates over extended cycling, allowing for scalable increase in areal capacity with electrode thickness. Our results demonstrate conformal nanoscale anode-electrolyte architectures for an efficient Li ion battery system.

  8. Lithium iron phosphate battery electrode integrity following high speed pulsed laser cutting

    Science.gov (United States)

    Lutey, Adrian H. A.; Fiorini, Maurizio; Fortunato, Alessandro; Carmignato, Simone

    2015-05-01

    Laser exposures are performed on lithium iron phosphate battery electrodes at with process parameters based on those leading to the smallest heat affected zone for low power laser exposure at . Scanning electron microscopy and Raman analysis are performed along the resulting cut edges to characterize macroscopic, chemical and microstructural changes resulting from laser exposure. The increase in velocity with respect to previous studies is found to limit macroscopic changes to areas directly exposed to the laser beam and greatly suppress or completely eliminate microstructural and chemical changes resulting from thermal conduction effects in the metallic conductor layers. These results confirm laser technology as a viable, more flexible solution to mechanical blanking devices for the cutting of lithium iron phosphate battery electrode films.

  9. Nanoscale Imaging of Lithium Ion Distribution During In Situ Operation of Battery Electrode and Electrolyte

    CERN Document Server

    Holtz, Megan E; Gunceler, Deniz; Gao, Jie; Sundararaman, Ravishankar; Schwarz, Kathleen A; Arias, Tomás A; Abruña, Héctor D; Muller, David A

    2013-01-01

    A major challenge in the development of new battery materials is understanding their fundamental mechanisms of operation and degradation. Their microscopically inhomogeneous nature calls for characterization tools that provide operando and localized information from individual grains and particles. Here we describe an approach that images the nanoscale distribution of ions during electrochemical charging of a battery in a transmission electron microscope liquid flow cell. We use valence energy-loss spectroscopy to track both solvated and intercalated ions, with electronic structure fingerprints of the solvated ions identified using an ab initio non-linear response theory. Equipped with the new electrochemical cell holder, nanoscale spectroscopy and theory, we have been able to determine the lithiation state of a LiFePO4 electrode and surrounding aqueous electrolyte in real time with nanoscale resolution during electrochemical charge and discharge. We follow lithium transfer between electrode and electrolyte a...

  10. Thermodynamic analysis and effect of crystallinity for silicon monoxide negative electrode for lithium ion batteries

    Science.gov (United States)

    Yasuda, Kouji; Kashitani, Yusuke; Kizaki, Shingo; Takeshita, Kohki; Fujita, Takehisa; Shimosaki, Shinji

    2016-10-01

    The electrochemical behavior of SiO negative electrodes for lithium ion batteries is thermodynamically and experimentally investigated. The analysis of the reaction pathway and the calculation of the reaction potentials during the Li insertion/extraction reactions are carried out by the construction of the ternary phase diagram for the Li-Si-O system. In the initial reaction of Li insertion, metallic Si and lithium silicates are formed above 0.37 V vs. Li/Li+ as a conversion reaction of the SiO negative electrode. Further Li insertion produces Li-Si alloys as reversible reaction phases. The decomposition of the Li4SiO4 phase begins before the formation of the Li-Si alloy is completed. The measured electrode behavior of the SiO negative electrode basically agrees with the thermodynamic calculations, especially at a low reaction rate; deviations can be ascribed to kinetic factors and electrode resistance. The values of over 1898 mA h g-1 and 71.0% were obtained for the discharge capacity and the coulombic efficiency, respectively. Furthermore, the overvoltage for an amorphous SiO electrode was smaller than that for a disproportionated SiO electrode into Si and SiO2 phases.

  11. Mechanism of Silicon Electrode Aging upon Cycling in Full Lithium-Ion Batteries.

    Science.gov (United States)

    Delpuech, Nathalie; Dupre, Nicolas; Moreau, Philippe; Bridel, Jean-Sebastian; Gaubicher, Joel; Lestriez, Bernard; Guyomard, Dominique

    2016-04-21

    Understanding the aging mechanism of silicon-based negative electrodes for lithium-ion batteries upon cycling is essential to solve the problem of low coulombic efficiency and capacity fading and further to implement this new high-capacity material in commercial cells. Nevertheless, such studies have so far focused on half cells in which silicon is cycled versus an infinite reservoir of lithium. In the present work, the aging mechanism of silicon-based electrodes is studied upon cycling in a full Li-ion cell configuration with LiCoO2 as the positive electrode. Postmortem analyses of both electrodes clearly indicate that neither one of them contains lithium and that no discernible degradation results from the cycling. The aging mechanism can be explained by the reduction of solvent molecules. Electrons extracted from the positive electrode are responsible for an internal imbalance in the cell, which results in progressive slippage of the electrodes and reduces the compositional range of cyclable lithium ions for both electrodes.

  12. Nanocomposite Electrodes for Advanced Lithium Batteries: The LiFePO4 Cathode

    Science.gov (United States)

    2001-11-01

    The LiFePO4 Cathode DISTRIBUTION: Approved for public release, distribution unlimited This paper is part of the following report: TITLE: Nanophase and...Nanocomposite Electrodes for Advanced Lithium Batteries: The LiFePO4 Cathode Shoufeng Yang, Yanning Song, Peter Y. Zavalij and M. Stanley Whittingham...Institute for Materials Research, Binghamton University, Binghamton, NY 13902-1600, U.S.A. ABSTRACT LiFePO4 was successfully synthesized by high temperature

  13. Enhanced performance of VRLA batteries with a novel spirally-wound electrode design

    Science.gov (United States)

    Wang, J.; Liu, H. K.; Dou, S. X.; Zhong, S.; Zhu, Y.; Fu, C.

    A spirally-wound electrode has been designed, constructed and applied to VRLA cells. Because of its unique construction: high strength, light-weight lead-coated glass fibre mesh as the grid, comparatively thin plates and sufficient internal compression, this new design provides significant advantages over the conventional prismatic type of VRLA battery. The total weight of grids and top lead used in a battery can be reduced by 40% compared with conventional cast grids. There was no positive active-material softening and expansion until after over 300 deep cycles. Substantial improvement in sustaining the cycleability has been achieved. This technique also provides a convenient process for manufacturing a spirally-wound VRLA battery in a simple and cost competitive way.

  14. Radiation effects on the electrode and electrolyte of a lithium-ion battery

    Science.gov (United States)

    Tan, Chuting; Lyons, Daniel J.; Pan, Ke; Leung, Kwan Yee; Chuirazzi, William C.; Canova, Marcello; Co, Anne C.; Cao, Lei R.

    2016-06-01

    The performance degradation and durability of a Li-ion battery is a major concern when it is operated under radiation conditions, for instance, in deep space exploration, in high radiation field, or rescuing or sampling equipment in a post-nuclear accident scenario. This paper examines the radiation effects on the electrode and electrolyte materials separately and their effects on a battery's capacity loss and resistance increase. A60Co irradiator (34.3 krad/h) was used to provide 0.8, 4.1, and 9.8 Mrad dose to LiFePO4 electrodes and 0.8, 1.6, and 5.7 Mrad to 1 M LiPF6 in 1:1 wt% EC:DMC electrolytes. This study shows that the coin cells assembled with irradiated components have higher failure rate (ca. 70%) than that of control group (ca. 14%). A significant battery capacity fade post irradiation was observed. The electrolyte also shows a darkened color a few weeks or months after irradiation. The discovery of this latent effect may be significant because a battery may degrade significantly even showing no sign of degradation immediately after exposure. We investigated electrolyte composition by Fourier transform infrared spectroscopy, ultraviolet-visible spectroscopy, and nuclear magnetic resonance spectroscopy prior and post irradiation. Polymerization reactions and HF formation are considered as the cause of the discoloration.

  15. Conical surface structures on model thin-film electrodes and tape-cast electrode materials for lithium-ion batteries

    Science.gov (United States)

    Kohler, R.; Proell, J.; Bruns, M.; Ulrich, S.; Seifert, H. J.; Pfleging, W.

    2013-07-01

    Three-dimensional structures in cathode materials for lithium-ion batteries were investigated in this study. For this purpose, laser structuring of lithium cobalt oxide was investigated at first for a thin-film model system and in a second step for conventional tape-cast electrode materials. The model thin-film cathodes with a thickness of 3 μm were deposited using RF magnetron sputtering on stainless steel substrates. The films were structured via excimer laser radiation with a wavelength of 248 nm. By adjusting the laser fluence, self-organized conical microstructures were formed. Using conventional electrodes, tape-cast cathodes made of LiCoO2 with a film thickness of about 80 μm on aluminum substrates were studied. It was shown that self-organizing surface structures could be formed by adjustment of the laser parameters. To investigate the formation mechanisms of the conical topography, the element composition was studied by time-of-flight secondary ion mass spectrometry and X-ray photoelectron spectroscopy. Electrochemical cycling using a lithium anode and conventional electrolyte was applied to study the influence of the laser processing procedures on cell performance. For the model electrode system, a significantly higher discharge capacity of 80 mAh/g could be obtained after 110 cycles by laser structuring compared to 8 mAh/g of the unstructured thin film. On conventional tape-cast electrodes self-organized surface structures could also increase the cycling stability resulting in an 80 % increase in capacity after 110 cycles in comparison to the unstructured electrode.

  16. Advanced porous electrodes with flow channels for vanadium redox flow battery

    Science.gov (United States)

    Bhattarai, Arjun; Wai, Nyunt; Schweiss, Ruediger; Whitehead, Adam; Lim, Tuti M.; Hng, Huey Hoon

    2017-02-01

    Improving the overall energy efficiency by reducing pumping power and improving flow distribution of electrolyte, is a major challenge for developers of flow batteries. The use of suitable channels can improve flow distribution through the electrodes and reduce flow resistance, hence reducing the energy consumption of the pumps. Although several studies of vanadium redox flow battery have proposed the use of bipolar plates with flow channels, similar to fuel cell designs, this paper presents the use of flow channels in the porous electrode as an alternative approach. Four types of electrodes with channels: rectangular open channel, interdigitated open cut channel, interdigitated circular poked channel and cross poked circular channels, are studied and compared with a conventional electrode without channels. Our study shows that interdigitated open channels can improve the overall energy efficiency up to 2.7% due to improvement in flow distribution and pump power reduction while interdigitated poked channel can improve up to 2.5% due to improvement in flow distribution.

  17. Surface modification of positive electrode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Julien, C.M., E-mail: Christian.Julien@upmc.fr [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Mauger, A. [Institut de Minéralogie de Physique des Matériaux et de Cosmochimie (IMPMC), UPMC Univ. Paris 6, 4 place Jussieu, 75005 Paris (France); Groult, H. [Sorbonne Universités, UPMC Univ. Paris 6, Physicochimie des Electrolytes et Nanosystèmes Interfaciaux (PHENIX), UMR 8234, 75005 Paris (France); Zaghib, K. [Energy Storage and Conversion, Research Institute of Hydro-Québec, Varennes, Québec J3X 1S1 (Canada)

    2014-12-01

    The advanced lithium-ion batteries are critically important for a wide range of applications, from portable electronics to electric vehicles. The research on their electrodes aims to increase the energy density and the power density, improve the calendar and the cycling life, without sacrificing the safety issues. A constant progress through the years has been obtained owing to the surface treatment of the particles, in particular the coating of the nanoparticles with a layer that protects the core region from side reactions with the electrolyte, prevents the loss of oxygen, and the dissolution of the metal ions in the electrolyte, or simply improve the conductivity of the powder. The purpose of the present work is to present the different surface modifications that have been tried for three families of positive electrodes: layered, spinel and olivine frameworks that are currently considered as promising materials. The role of the different coats used to improve either the surface conductivity, or the thermal stability, or the structural integrity is discussed. - Highlights: • Report the various surface modifications tried for the positive electrodes of Li-ion batteries. • The role of different coats used to improve the conductivity, or the thermal stability, or the structural integrity. • Improvement of electrochemical properties of electrodes after coating or surface treatment.

  18. Microwave-treated graphite felt as the positive electrode for all-vanadium redox flow battery

    Science.gov (United States)

    Wu, Xiaoxin; Xu, Hongfeng; Xu, Pengcheng; Shen, Yang; Lu, Lu; Shi, Jicheng; Fu, Jie; Zhao, Hong

    2014-10-01

    An environmental, economic, and highly effective method based on microwave treatment was firstly used to improve the electrochemical activity of graphite felt as the positive electrode in all vanadium redox flow battery (VRFB). The graphite felt was treated by microwave and characterized by Fourier transform infrared and scanning electron microscopy. The electrochemical performance of the prepared electrode was evaluated with cyclic voltammetry and electrochemical impedance spectroscopy. Results show that graphite felt treated by microwave for 15 min at 400 °C exhibits excellent electro-catalytic activity and reactive velocity to vanadium redox couples. The coulombic, voltage, and energy efficiency of the VRFB with as-prepared electrodes at 50 mA cm-2 are 96.9%, 75.5%, and 73.2%, respectively; these values are much higher than those of cell-assembled conventionally and thermally treated graphite felt electrodes. The microwave-treated graphite felt will carry more hydrophilic groups, such as -OH, on its defects, and rough degree of the surface which should be advantageous in facilitating the redox reaction of vanadium ions, leading to the efficient operation of a vanadium redox flow battery. Moreover, microwave treatment can be easily scaled up to treat graphite felt for VRFB in large quantities.

  19. The fabrication of a bifunctional oxygen electrode without carbon components for alkaline secondary batteries

    Science.gov (United States)

    Price, Stephen W. T.; Thompson, Stephen J.; Li, Xiaohong; Gorman, Scott F.; Pletcher, Derek; Russell, Andrea E.; Walsh, Frank C.; Wills, Richard G. A.

    2014-08-01

    The fabrication of a gas diffusion electrode (GDE) without carbon components is described. It is therefore suitable for use as a bifunctional oxygen electrode in alkaline secondary batteries. The electrode is fabricated in two stages (a) the formation of a PTFE-bonded nickel powder layer on a nickel foam substrate and (b) the deposition of a NiCo2O4 spinel electrocatalyst layer by dip coating in a nitrate solution and thermal decomposition. The influence of modifications to the procedure on the performance of the GDEs in 8 M NaOH at 333 K is described. The GDEs can support current densities up to 100 mA cm-2 with state-of-the-art overpotentials for both oxygen evolution and oxygen reduction. Stable performance during >50 successive, 1 h oxygen reduction/evolution cycles at a current density of 50 mA cm-2 has been achieved.

  20. A high-performance dual-scale porous electrode for vanadium redox flow batteries

    Science.gov (United States)

    Zhou, X. L.; Zeng, Y. K.; Zhu, X. B.; Wei, L.; Zhao, T. S.

    2016-09-01

    In this work, we present a simple and cost-effective method to form a dual-scale porous electrode by KOH activation of the fibers of carbon papers. The large pores (∼10 μm), formed between carbon fibers, serve as the macroscopic pathways for high electrolyte flow rates, while the small pores (∼5 nm), formed on carbon fiber surfaces, act as active sites for rapid electrochemical reactions. It is shown that the Brunauer-Emmett-Teller specific surface area of the carbon paper is increased by a factor of 16 while maintaining the same hydraulic permeability as that of the original carbon paper electrode. We then apply the dual-scale electrode to a vanadium redox flow battery (VRFB) and demonstrate an energy efficiency ranging from 82% to 88% at current densities of 200-400 mA cm-2, which is record breaking as the highest performance of VRFB in the open literature.

  1. Graphite felt modified with bismuth nanoparticles as negative electrode in a vanadium redox flow battery.

    Science.gov (United States)

    Suárez, David J; González, Zoraida; Blanco, Clara; Granda, Marcos; Menéndez, Rosa; Santamaría, Ricardo

    2014-03-01

    A graphite felt decorated with bismuth nanoparticles was studied as negative electrode in a vanadium redox flow battery (VRFB). The results confirm the excellent electrochemical performance of the bismuth modified electrode in terms of the reversibility of the V(3+) /V(2+) redox reactions and its long-term cycling performance. Moreover a mechanism that explains the role that Bi nanoparticles play in the redox reactions in this negative half-cell is proposed. Bi nanoparticles favor the formation of BiHx , an intermediate that reduces V(3+) to V(2+) and, therefore, inhibits the competitive irreversible reaction of hydrogen formation (responsible for the commonly observed loss of Coulombic efficiency of VRFBs). Thus, the total charge consumed during the cathodic sweep in this electrode is used to reduce V(3+) to V(2+) , resulting in a highly reversible and efficient process.

  2. Highly accurate apparatus for electrochemical characterization of the felt electrodes used in redox flow batteries

    Science.gov (United States)

    Park, Jong Ho; Park, Jung Jin; Park, O. Ok; Jin, Chang-Soo; Yang, Jung Hoon

    2016-04-01

    Because of the rise in renewable energy use, the redox flow battery (RFB) has attracted extensive attention as an energy storage system. Thus, many studies have focused on improving the performance of the felt electrodes used in RFBs. However, existing analysis cells are unsuitable for characterizing felt electrodes because of their complex 3-dimensional structure. Analysis is also greatly affected by the measurement conditions, viz. compression ratio, contact area, and contact strength between the felt and current collector. To address the growing need for practical analytical apparatus, we report a new analysis cell for accurate electrochemical characterization of felt electrodes under various conditions, and compare it with previous ones. In this cell, the measurement conditions can be exhaustively controlled with a compression supporter. The cell showed excellent reproducibility in cyclic voltammetry analysis and the results agreed well with actual RFB charge-discharge performance.

  3. A novel slurry concept for the fabrication of lithium-ion battery electrodes with beneficial properties

    Science.gov (United States)

    Bitsch, Boris; Dittmann, Jens; Schmitt, Marcel; Scharfer, Philip; Schabel, Wilhelm; Willenbacher, Norbert

    2014-11-01

    A novel slurry concept for the fabrication of Li-ion battery electrodes focusing on water based formulations is presented. Taking advantage of capillary forces inferred by adding a small fraction of a second fluid immiscible with the bulk continuous phase the low shear viscosity can be varied in a wide range without conventional polymeric rheology control agents disturbing the electric properties of the dry electrode. The new slurries provide superior storage stability and excellent shape accuracy of the final dry film. This reduces waste cut-off at the edges and increases the density of active ingredients, thus improving cost-efficiency. The viscosity at high shear rates remains unaffected, thus the slurries can be processed and coated using established equipment and process parameters. Adhesion to the conductor foil and electrochemical properties of the electrode layers and corresponding cells are similar to those made from conventional slurries.

  4. Transient three-dimensional thermal model for batteries with thin electrodes

    Science.gov (United States)

    Taheri, Peyman; Yazdanpour, Maryam; Bahrami, Majid

    2013-12-01

    A three-dimensional analytical model is proposed to investigate the thermal response of batteries, with a plurality of thin electrodes, to heat generation during their operation. The model is based on integral-transform technique that gives a closed-form solution for the fundamental problem of unsteady heat conduction in batteries with orthotropic thermal conductivities, where the heat generation is a function of both temperature and depth-of-discharge. The full-field solutions take the form of a rapidly converging triple infinite sum whose leading terms provide a very simple yet accurate approximation of the battery thermal behavior with modest numerical effort. The accuracy of the proposed model is tested through comparison with numerical simulations. The method is used to describe spatial and temporal temperature evolution in a sample pouch type lithium-ion polymer battery during galvanostatic discharge processes while subjected to convective-radiative cooling at its surfaces (the most practical case is considered, when surrounding medium is at a constant ambient temperature). In the simulations, emphasis is placed on the maintenance of the battery operational temperature below a critical temperature. Through definition of a surface-averaged Biot number, certain conditions are highlighted, under which a two-dimensional thermal analysis is applicable.

  5. Vertical distribution of overpotentials and irreversible charge losses in lithium ion battery electrodes.

    Science.gov (United States)

    Klink, Stefan; Schuhmann, Wolfgang; La Mantia, Fabio

    2014-08-01

    Porous lithium ion battery electrodes are characterized using a vertical distribution of cross-currents. In an appropriate simplification, this distribution can be described by a transmission line model (TLM) consisting of infinitely thin electrode layers. To investigate the vertical distribution of currents, overpotentials, and irreversible charge losses in a porous graphite electrode in situ, a multi-layered working electrode (MWE) was developed as the experimental analogue of a TLM. In this MWE, each layer is in ionic contact but electrically insulated from the other layers by a porous separator. It was found that the negative graphite electrodes get lithiated and delithiated stage-by-stage and layer-by-layer. Several mass-transport- as well as non-mass-transport-limited processes could be identified. Local current densities can reach double the average, especially on the outermost layer at the beginning of each intercalation stage. Furthermore, graphite particles close to the counter electrode act as "electrochemical sieve" reducing the impurities present in the electrolyte such as water.

  6. SnCo nanowire array as negative electrode for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Ferrara, Germano; Inguanta, Rosalinda; Piazza, Salvatore; Sunseri, Carmelo [Universita degli Studi di Palermo, Dipartimento di Ingegneria Chimica dei Processi e dei Materiali, Viale delle Scienze Ed. 6, 90128 Palermo (Italy); Damen, Libero; Arbizzani, Catia; Mastragostino, Marina [Universita degli Studi di Bologna, Dipartimento di Scienza dei Metalli, Elettrochimica e Tecniche Chimiche, Via San Donato 15, 40127 Bologna (Italy)

    2011-02-01

    Amorphous SnCo alloy nanowires (NWs) grown inside the channels of polycarbonate membranes by potentiostatic codeposition of the two metals (SnCo-PM) were tested vs. Li by repeated galvanostatic cycles in ethylene carbonate-dimethylcarbonate - LiPF{sub 6} for use as negative electrode in lithium ion batteries. These SnCo electrodes delivered an almost constant capacity value, near to the theoretical for an atomic ratio Li/Sn of 4.4 over more than 35 lithiation-delithiation cycles at 1 C. SEM images of fresh and cycled electrodes showed that nanowires remain partially intact after repeated lithiation-delithiation cycles; indeed, several wires expanded and became porous. Results of amorphous SnCo nanowires grown inside anodic alumina membranes (SnCo-AM) are also reported. The comparison of the two types of NW electrodes demonstrates that the morphology of the SnCo-PM is more suitable than that of the SnCo-AM for electrode stability over cycling. Optimization of NW technology should thus be a promising route to enhancing the mechanical strength and durability of tin-based electrodes. (author)

  7. Electrospun carbon nanofibers/electrocatalyst hybrids as asymmetric electrodes for vanadium redox flow battery

    Science.gov (United States)

    Wei, Guanjie; Fan, Xinzhuang; Liu, Jianguo; Yan, Chuanwei

    2015-05-01

    To improve the electrochemical activity of polyacrylonitrile (PAN)-based electrospun carbon nanofibers (ECNFs) toward vanadium redox couples, the multi-wall carbon nanotubes (CNTs) and Bi-based compound as electrocatalyst have been embedded in the ECNFs to make composite electrode, respectively. The morphology and electrochemical properties of pristine ECNFs, CNTs/ECNFs and Bi/ECNFs have been characterized. Among the three kinds of electrodes, the CNTs/ECNFs show best electrochemical activity toward VO2+/VO2+ redox couple, while the Bi/ECNFs present the best electrochemical activity toward V2+/V3+ redox couple. Furthermore, the high overpotential of hydrogen evolution on Bi/ECNFs makes the side-reaction suppressed. Because of the large property difference between the two composite electrodes, the CNTs/ECNFs and Bi/ECNFs are designed to act as positive and negative electrode for vanadium redox flow battery (VRFB), respectively. It not only does improve the kinetics of two electrode reactions at the same time, but also reduce the kinetics difference between them. Due to the application of asymmetric electrodes, performance of the cell is improved greatly.

  8. Elegant design of electrode and electrode/electrolyte interface in lithium-ion batteries by atomic layer deposition

    Science.gov (United States)

    Liu, Jian; Sun, Xueliang

    2015-01-01

    Lithium-ion batteries (LIBs) are very promising power supply systems for a variety of applications, such as electric vehicles, plug-in hybrid electric vehicles, grid energy storage, and microelectronics. However, to realize these practical applications, many challenges need to be addressed in LIBs, such as power and energy density, cycling lifetime, safety, and cost. Atomic layer deposition (ALD) is emerging as a powerful technique for solving these problems due to its exclusive advantages over other film deposition counterparts. In this review, we summarize the state-of-the-art progresses of employing ALD to design novel nanostructured electrode materials and solid-state electrolytes and to tailor electrode/electrolyte interface by surface coatings in order to prevent unfavorable side reactions and achieve optimal performance of the electrode. Insights into the future research and development of the ALD technique for LIB applications are also discussed. We expect that this review article will provide resourceful information to researchers in both fields of LIBs and ALD and also will stimulate more insightful studies of using ALD for the development of next-generation LIBs.

  9. Chemical and microstructural transformations in lithium iron phosphate battery electrodes following pulsed laser exposure

    Energy Technology Data Exchange (ETDEWEB)

    Lutey, Adrian H.A., E-mail: adrian.lutey2@unibo.it [DIN, Università di Bologna, viale Risorgimento, 2, Bologna (Italy); Fiorini, Maurizio [DICAM, Università di Bologna, via Terracini, 28, Bologna (Italy); Fortunato, Alessandro; Ascari, Alessandro [DIN, Università di Bologna, viale Risorgimento, 2, Bologna (Italy)

    2014-12-15

    Highlights: • Lithium iron phosphate battery electrodes are exposed to pulsed laser radiation. • Raman spectroscopy is performed on regions approaching the incisions and cuts. • Chemical and microstructural changes in the active electrode layers are limited to the visible HAZ. • Some oxidation and degradation of the olive LiFePO{sub 4} cathode active material takes place in the HAZ. • The anode polycrystalline graphite structure becomes less ordered (higher D/G ratio) in the HAZ. - Abstract: Multi-layer lithium iron phosphate (LFP) battery electrodes are exposed to nanosecond pulsed laser radiation of wavelength 1064 nm. Test parameters are chosen to achieve characteristic interaction types ranging from partial incision of the active coating layers only to complete penetration of the electrodes with high visual cut quality. Raman spectroscopy is performed on unexposed regions and at points approaching each incision, highlighting changes in chemical composition and microstructure in the heat affected zone (HAZ). Thermogravimetric analysis is performed on the unexposed electrode active materials to distinguish the development of compositional changes under conditions of slow heating below the melting and sublimation temperatures. A brief theoretical description of the physical phenomena taking place during laser exposure is provided in terms of direct ablation during each laser pulse and vaporization or thermal degradation due to conductive heat transfer on a much longer time-scale, with characteristics of the HAZ reported in terms of these changes. For all laser exposures carried out in the study, chemical and microstructural changes are limited to the visible HAZ. Some degree of oxidation and LFP olivine phase degradation is observed in the cathode, while the polycrystalline graphite structure becomes less ordered in the anode. Where complete penetration is achieved, melting of the cathode active layer and combustion of the anode active layer take place

  10. Operando studies of all-vanadium flow batteries: Easy-to-make reference electrode based on silver-silver sulfate

    Science.gov (United States)

    Ventosa, Edgar; Skoumal, Marcel; Vázquez, Francisco Javier; Flox, Cristina; Morante, Joan Ramon

    2014-12-01

    In-depth evaluation of the electrochemical performance of all-vanadium redox flow batteries (VRFBs) under operando conditions requires the insertion of a reliable reference electrode in the battery cell. In this work, an easy-to-make reference electrode based on silver-silver sulfate is proposed and described for VRFBs. The relevance and feasibility of the information obtained by inserting the reference electrode is illustrated with the study of ammoxidized graphite felts. In this case, we show that the kinetic of the electrochemical reaction VO2+/VO2+ is slower than that of V2+/V3+ at the electrode. While the slow kinetics at the positive electrode limits the voltage efficiency, the operating potential of the negative electrode, which is outside the stability widow of water, reduces the coulombic efficiency due to the hydrogen evolution.

  11. From biomass to a renewable LixC6O6 organic electrode for sustainable Li-ion batteries.

    Science.gov (United States)

    Chen, Haiyan; Armand, Michel; Demailly, Gilles; Dolhem, Franck; Poizot, Philippe; Tarascon, Jean-Marie

    2008-01-01

    Li-ion batteries presently operate on inorganic insertion compounds. The abundance and materials life-cycle costs of such batteries may present issues in the long term with foreseeable large-scale applications. To address the issue of sustainability of electrode materials, a radically different approach from the conventional route has been adopted to develop new organic electrode materials. The oxocarbon salt Li2C6O6 is synthesized through potentially low-cost processes free of toxic solvents and by enlisting the use of natural organic sources (CO2-harvesting entities). It contains carbonyl groups as redox centres and can electrochemically react with four Li ions per formula unit. Such battery processing comes close to both sustainable and green chemistry concepts, which are not currently present in Li-ion cell technology. The consideration of renewable resources in designing electrode materials could potentially enable the realization of green and sustainable batteries within the next decade.

  12. Multi-band reflectance spectroscopy of carbonaceous lithium iron phosphate battery electrodes versus state of charge

    Science.gov (United States)

    Norris, R.; Iyer, K.; Chabot, V.; Nieva, P.; Yu, A.; Khajepour, A.; Wang, J.

    2014-03-01

    This study aims to expand the body of knowledge about the optical properties of battery cathode materials. Although some studies have been conducted on the optical properties of Lithium Iron Phosphate (LiFePO4), to the authors' knowledge, this is the first study of its kind on electrodes extracted from commercially available LiFePO4 batteries. The use of Vis/NIR and FTIR spectroscopy provides for a methodology to study the optical properties of LiFePO4 and may allow for the characterization of other properties such as particle size and the proportions of LiFePO4 versus FePO4 material. Knowledge of these properties is important for the development of a mechanism to measure the state-of charge (SOC) in lithium ion batteries. These properties are also important in a host of other applications including battery modeling and materials characterization. Cylindrical LiFePO4 batteries (from A123 Systems Inc.) were acquired from the commercial market and charged to 10 different states between 30% and 80% of their nominal capacity using a constant-current, constant-voltage (CCCV) cycling method. Visual inspection of the extracted electrodes shows that the LiFePO4/C-cathodes display subtle changes in color (shades of grey) with respect to SOC. Vis/NIR measurements support the visual observation of uniform intensity variations versus SOC. FTIR measurements show an absorbance signature that varies with SOC and is distinct from results found in the literature for similar LiFePO4-based material systems, supporting the uniqueness of the absorbance fingerprint.

  13. In-situ Spectroscopic and Structural Studies of Electrode Materials for Advanced Battery Applications

    Energy Technology Data Exchange (ETDEWEB)

    Daniel A Scherson

    2013-03-14

    Techniques have been developed and implemented to gain insight into fundamental factors that affect the performance of electrodes in Li and Li-ion batteries and other energy storage devices. These include experimental strategies for monitoring the Raman scattering spectra of single microparticles of carbon and transition metal oxides as a function of their state of charge. Measurements were performed in electrolytes of direct relevance to Li and Li-Ion batteries both in the static and dynamic modes. In addition, novel strategies were devised for performing conventional experiments in ultrahigh vacuum environments under conditions which eliminate effects associated with presence of impurities, using ultrapure electrolytes, both of the polymeric and ionic liquid type that display no measurable vapor pressure. Also examined was the reactivity of conventional non aqueous solvent toward ultrapure Li films as monitored in ultrahigh vacuum with external reflection Fourier transform infrared spectroscopy. Also pursued were efforts toward developing applying Raman-scattering for monitoring the flow of charge of a real Li ion battery. Such time-resolved, spatially-resolved measurements are key to validating the results of theoretical simulations involving real electrode structures.

  14. Bridging Redox Species-Coated Graphene Oxide Sheets to Electrode for Extending Battery Life Using Nanocomposite Electrolyte.

    Science.gov (United States)

    Huang, Yi Fu; Ruan, Wen Hong; Lin, Dong Ling; Zhang, Ming Qiu

    2017-01-11

    Substituting conventional electrolyte for redox electrolyte has provided a new intriguing method for extending battery life. The efficiency of utilizing the contained redox species (RS) in the redox electrolyte can benefit from increasing the specific surface area of battery electrodes from the electrode side of the electrode-electrolyte interface, but is not limited to that. Herein, a new strategy using nanocomposite electrolyte is proposed to enlarge the interface with the aid of nanoinclusions from the electrolyte side. To do this, graphene oxide (GO) sheets are first dispersed in the electrolyte solution of tungstosilicic salt/lithium sulfate/poly(vinyl alcohol) (SiWLi/Li2SO4/PVA), and then the sheets are bridged to electrode, after casting and evaporating the solution on the electrode surface. By applying in situ conductive atomic force microscopy and Raman spectra, it is confirmed that the GO sheets doped with RS of SiWLi/Li2SO4 can be bridged and electrically reduced as an extended electrode-electrolyte interface. As a result, the RS-coated GO sheets bridged to LiTi2(PO4)3//LiMn2O4 battery electrodes are found to deliver extra energy capacity (∼30 mAh/g) with excellent electrochemical cycling stability, which successfully extends the battery life by over 50%.

  15. Capillary suspensions as beneficial formulation concept for high energy density Li-ion battery electrodes

    Science.gov (United States)

    Bitsch, Boris; Gallasch, Tobias; Schroeder, Melanie; Börner, Markus; Winter, Martin; Willenbacher, Norbert

    2016-10-01

    We introduce a novel formulation concept to prepare high capacity graphite electrodes for lithium ion batteries. The concept is based on the capillary suspension phenomenon: graphite and conductive agent are dispersed in an aqueous binder solution and the organic solvent octanol is added as immiscible, secondary fluid providing the formation of a sample-spanning network resulting in unique stability and coating properties. No additional processing steps compared to conventional slurry preparation are required. The resulting ultra-thick electrodes comprise mass loadings of about 16.5 mg cm-2, uniform layer thickness, and superior edge contours. The adjustment of mechanical energy input ensures uniform distribution of the conductive agent and sufficient electronic conductivity of the final dry composite electrode. The resulting pore structure is due to the stable network provided by the secondary fluid which evaporates residue-free during drying. Constant current-constant potential (CC-CP) cycling clearly indicates that the corresponding microstructure significantly improves the kinetics of reversible Li+ (de-) intercalation. A double layer electrode combining a conventionally prepared layer coated directly onto the Cu current collector with an upper layer stabilized with octanol was prepared applying wet-on-wet coating. CC-CP cycling data confirms that staged porosity within the electrode cross section results in superior electrochemical performance.

  16. Recent improvements in PbO2 nanowire electrodes for lead-acid battery

    Science.gov (United States)

    Moncada, Alessandra; Piazza, Salvatore; Sunseri, Carmelo; Inguanta, Rosalinda

    2015-02-01

    Lead oxide nanowires are an attractive alternative to conventional pasted electrodes, owing to their high surface area leading to high specific energy batteries. Here, we report the performance of template electrodeposited PbO2 nanowires used as positive electrodes. Nanostructured electrodes were tested at constant charge/discharge rate from 2 C to 10 C, with a cut-off potential of 1.2 V and discharge depth up to 90% of the gravimetric charge. These new type of electrodes are able to work at very high C-rate without fading, reaching an efficiency of about 90% with a very good cycling stability. In particular, after an initial stabilization, a specific capacity of about 200 mAh g-1, very close to the theoretical one of 224 mAh g-1, was drained for more than 1000 cycles at a C-rate higher than 1 C with an efficiency close to 90%. This behaviour significantly distinguishes PbO2 nanostructured electrodes from the conventional ones with pasted active material. In addition, discharge at a quasi-constant voltage of about 2.1 V, without reaching the cut-off potential also at high C-rate, occurs. This implies a quasi-constant energy supply during fast discharge. According to these findings, innovative applications as hybrid or electrical mobility or buffer in renewable energy plants can be envisaged.

  17. Water-activated graphite felt as a high-performance electrode for vanadium redox flow batteries

    Science.gov (United States)

    Kabtamu, Daniel Manaye; Chen, Jian-Yu; Chang, Yu-Chung; Wang, Chen-Hao

    2017-02-01

    A simple, green, novel, time-efficient, and potentially cost-effective water activation method was employed to enhance the electrochemical activity of graphite felt (GF) electrodes for vanadium redox flow batteries (VRFBs). The GF electrode prepared with a water vapor injection time of 5 min at 700 °C exhibits the highest electrochemical activity for the VO2+/VO2+ couple among all the tested electrodes. This is attributed to the small, controlled amount of water vapor that was introduced producing high contents of oxygen-containing functional groups, such as sbnd OH groups, on the surface of the GF fibers, which are known to be electrochemically active sites for vanadium redox reactions. Charge-discharge tests further confirm that only 5 min of GF water activation is required to improve the efficiency of the VRFB cell. The average coulombic efficiency, voltage efficiency, and energy efficiency are 95.06%, 87.42%, and 83.10%, respectively, at a current density of 50 mA cm-2. These voltage and energy efficiencies are determined to be considerably higher than those of VRFB cells assembled using heat-treated GF electrodes without water activation and pristine GF electrodes.

  18. Local state-of-charge mapping of lithium-ion battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Nanda, Jagjit [Materials Science and Technology Division, Oak Ridge National Laboratory, Oak Ridge, TN (United States); Remillard, Jeffrey; O' Neill, Ann; Bernardi, Dawn; Ro, Tina; Nietering, Kenneth E.; Miller, Ted J. [Research and Advanced Engineering, Ford Motor Co., Dearborn, MI (United States); Go, Joo-Young [SB LiMotive, R and D Team, Gyeonggi-do (Korea, Republic of)

    2011-09-09

    Current lithium-ion battery technology is gearing towards meeting the robust demand of power and energy requirements for all-electric transportation without compromising on the safety, performance, and cycle life. The state-of-charge (SOC) of a Li-ion cell can be a macroscopic indicator of the state-of-health of the battery. The microscopic origin of the SOC relates to the local lithium content in individual electrode particles and the effective ability of Li-ions to transport or shuttle between the redox couples through the cell geometric boundaries. Herein, micrometer-resolved Raman mapping of a transition-metal-based oxide positive electrode, Li{sub 1-x}(Ni{sub y}Co{sub z}Al{sub 1-y-z})O{sub 2}, maintained at different SOCs, is shown. An attempt has been made to link the underlying changes to the composition and structural integrity at the individual particle level. Furthermore, an SOC distribution at macroscopic length scale of the electrodes is presented. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  19. Fabrication and characterization of three-dimensional carbon electrodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Teixidor, Genis Turon; Zaouk, Rabih B.; Park, Benjamin Y.; Madou, Marc J. [Department of Mechanical and Aerospace Engineering, 4200 Engineering Gateway Building, University of California, Irvine, Irvine, CA 92697 (United States)

    2008-09-01

    This paper presents fabrication and testing results of three-dimensional carbon anodes for lithium-ion batteries, which are fabricated through the pyrolysis of lithographically patterned epoxy resins. This technique, known as Carbon-MEMS, provides great flexibility and an unprecedented dimensional control in shaping carbon microstructures. Variations in the pattern density and in the pyrolysis conditions result in anodes with different specific and gravimetric capacities, with a three to six times increase in specific capacity with respect to the current thin-film battery technology. Newly designed cross-shaped Carbon-MEMS arrays have a much higher mechanical robustness (as given by their moment of inertia) than the traditionally used cylindrical posts, but the gravimetric analysis suggests that new designs with thinner features are required for better carbon utilization. Pyrolysis at higher temperatures and slower ramping up schedules reduces the irreversible capacity of the carbon electrodes. We also analyze the addition of Meso-Carbon Micro-Beads (MCMB) particles on the reversible and irreversible capacities of new three-dimensional, hybrid electrodes. This combination results in a slight increase in reversible capacity and a big increase in the irreversible capacity of the carbon electrodes, mostly due to the non-complete attachment of the MCMB particles. (author)

  20. Biomimetic Ant-Nest Electrode Structures for High Sulfur Ratio Lithium-Sulfur Batteries.

    Science.gov (United States)

    Ai, Guo; Dai, Yiling; Mao, Wenfeng; Zhao, Hui; Fu, Yanbao; Song, Xiangyun; En, Yunfei; Battaglia, Vincent S; Srinivasan, Venkat; Liu, Gao

    2016-09-14

    The lithium-sulfur (Li-S) rechargeable battery has the benefit of high gravimetric energy density and low cost. Significant research currently focuses on increasing the sulfur loading and sulfur/inactive-materials ratio, to improve life and capacity. Inspired by nature's ant-nest structure, this research results in a novel Li-S electrode that is designed to meet both goals. With only three simple manufacturing-friendly steps, which include slurry ball-milling, doctor-blade-based laminate casting, and the use of the sacrificial method with water to dissolve away table salt, the ant-nest design has been successfully recreated in an Li-S electrode. The efficient capabilities of the ant-nest structure are adopted to facilitate fast ion transportation, sustain polysulfide dissolution, and assist efficient precipitation. High cycling stability in the Li-S batteries, for practical applications, has been achieved with up to 3 mg·cm(-2) sulfur loading. Li-S electrodes with up to a 85% sulfur ratio have also been achieved for the efficient design of this novel ant-nest structure.

  1. Reinstating lead for high-loaded efficient negative electrode for rechargeable sodium-ion battery

    Science.gov (United States)

    Darwiche, Ali; Dugas, Romain; Fraisse, Bernard; Monconduit, Laure

    2016-02-01

    Due to its weight and toxicity, Pb is usually not considered as possible anode for Li- and Na-ion (NIBs) batteries. Nevertheless the toxicity is related to specific applications and its recycling is more than 99% which is one of the highest recycling rates on the planet where no other power source is utilized in more applications with such sustainability. For this reason, we have investigated micrometric lead particles as electrode for NIBs in an ether-based electrolyte (1 M NaPF6 in diglyme). The cyclability, coulombic efficiency and rate capability of lead were unexpected. A high loaded lead electrode with 98%wt of Pb and only 1% of carbon additive showed i) a capacity retention of 464 mA h/g after 50 cycles with only 1.5% of capacity loss, which represents a high volumetric capacity of 5289 mA h/cm3 due to the high density of Pb and ii) a very interesting capacity retention even at high current rate (1950 mA/g). In situ XRD study confirmed a sodiation-desodiation process in four steps. Preliminary tests in Pb//Na3V2(PO4)2F3 full cells showed promising results demonstrating that Pb could be a practical candidate for future high energy density Na-ion batteries with an efficient sodiated or non sodiated positive electrode.

  2. The application of phase contrast X-ray techniques for imaging Li-ion battery electrodes

    Science.gov (United States)

    Eastwood, D. S.; Bradley, R. S.; Tariq, F.; Cooper, S. J.; Taiwo, O. O.; Gelb, J.; Merkle, A.; Brett, D. J. L.; Brandon, N. P.; Withers, P. J.; Lee, P. D.; Shearing, P. R.

    2014-04-01

    In order to accelerate the commercialization of fuel cells and batteries across a range of applications, an understanding of the mechanisms by which they age and degrade at the microstructural level is required. Here, the most widely commercialized Li-ion batteries based on porous graphite based electrodes which de/intercalate Li+ ions during charge/discharge are studied by two phase contrast enhanced X-ray imaging modes, namely in-line phase contrast and Zernike phase contrast at the micro (synchrotron) and nano (laboratory X-ray microscope) level, respectively. The rate of charge cycling is directly dependent on the nature of the electrode microstructure, which are typically complex multi-scale 3D geometries with significant microstructural heterogeneities. We have been able to characterise the porosity and the tortuosity by micro-CT as well as the morphology of 5 individual graphite particles by nano-tomography finding that while their volume varied significantly their sphericity was surprisingly similar. The volume specific surface areas of the individual grains measured by nano-CT are significantly larger than the total volume specific surface area of the electrode from the micro-CT imaging, which can be attributed to the greater particle surface area visible at higher resolution.

  3. Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes

    Science.gov (United States)

    Reddy, Arava Leela Mohana; Nagarajan, Subbiah; Chumyim, Porramate; Gowda, Sanketh R.; Pradhan, Padmanava; Jadhav, Swapnil R.; Dubey, Madan; John, George; Ajayan, Pulickel M.

    2012-12-01

    Current lithium batteries operate on inorganic insertion compounds to power a diverse range of applications, but recently there is a surging demand to develop environmentally friendly green electrode materials. To develop sustainable and eco-friendly lithium ion batteries, we report reversible lithium ion storage properties of a naturally occurring and abundant organic compound purpurin, which is non-toxic and derived from the plant madder. The carbonyl/hydroxyl groups present in purpurin molecules act as redox centers and reacts electrochemically with Li-ions during the charge/discharge process. The mechanism of lithiation of purpurin is fully elucidated using NMR, UV and FTIR spectral studies. The formation of the most favored six membered binding core of lithium ion with carbonyl groups of purpurin and hydroxyl groups at C-1 and C-4 positions respectively facilitated lithiation process, whereas hydroxyl group at C-2 position remains unaltered.

  4. All-vanadium redox flow batteries with graphite felt electrodes treated by atmospheric pressure plasma jets

    Science.gov (United States)

    Chen, Jian-Zhang; Liao, Wei-Yang; Hsieh, Wen-Yen; Hsu, Cheng-Che; Chen, Yong-Song

    2015-01-01

    Graphite felts modified with atmospheric pressure plasma jets (APPJs) are applied as electrodes in an all-vanadium redox flow battery (VRFB). APPJ flow penetrates deeply into the graphite felt, improving significantly the wettability of the graphite felt inside out and, thereby, enhancing graphite fiber-electrolyte contact during battery operation. The energy efficiency of a VRFB was improved from 62% (untreated) to 76% (APPJ-treated with the scan mode) at a current density of 80 mA cm-2, an improvement of 22%. The efficiency improvement is attributed to the oxygen-containing groups and nitrogen doping introduced by N2 APPJs on the fiber surfaces of graphite felt, both of which enhance electrochemical reactivity.

  5. Lithium storage mechanisms in purpurin based organic lithium ion battery electrodes.

    Science.gov (United States)

    Reddy, Arava Leela Mohana; Nagarajan, Subbiah; Chumyim, Porramate; Gowda, Sanketh R; Pradhan, Padmanava; Jadhav, Swapnil R; Dubey, Madan; John, George; Ajayan, Pulickel M

    2012-01-01

    Current lithium batteries operate on inorganic insertion compounds to power a diverse range of applications, but recently there is a surging demand to develop environmentally friendly green electrode materials. To develop sustainable and eco-friendly lithium ion batteries, we report reversible lithium ion storage properties of a naturally occurring and abundant organic compound purpurin, which is non-toxic and derived from the plant madder. The carbonyl/hydroxyl groups present in purpurin molecules act as redox centers and reacts electrochemically with Li-ions during the charge/discharge process. The mechanism of lithiation of purpurin is fully elucidated using NMR, UV and FTIR spectral studies. The formation of the most favored six membered binding core of lithium ion with carbonyl groups of purpurin and hydroxyl groups at C-1 and C-4 positions respectively facilitated lithiation process, whereas hydroxyl group at C-2 position remains unaltered.

  6. Comparison of three-dimensional analysis and stereological techniques for quantifying lithium-ion battery electrode microstructures.

    Science.gov (United States)

    Taiwo, Oluwadamilola O; Finegan, Donal P; Eastwood, David S; Fife, Julie L; Brown, Leon D; Darr, Jawwad A; Lee, Peter D; Brett, Daniel J L; Shearing, Paul R

    2016-09-01

    Lithium-ion battery performance is intrinsically linked to electrode microstructure. Quantitative measurement of key structural parameters of lithium-ion battery electrode microstructures will enable optimization as well as motivate systematic numerical studies for the improvement of battery performance. With the rapid development of 3-D imaging techniques, quantitative assessment of 3-D microstructures from 2-D image sections by stereological methods appears outmoded; however, in spite of the proliferation of tomographic imaging techniques, it remains significantly easier to obtain two-dimensional (2-D) data sets. In this study, stereological prediction and three-dimensional (3-D) analysis techniques for quantitative assessment of key geometric parameters for characterizing battery electrode microstructures are examined and compared. Lithium-ion battery electrodes were imaged using synchrotron-based X-ray tomographic microscopy. For each electrode sample investigated, stereological analysis was performed on reconstructed 2-D image sections generated from tomographic imaging, whereas direct 3-D analysis was performed on reconstructed image volumes. The analysis showed that geometric parameter estimation using 2-D image sections is bound to be associated with ambiguity and that volume-based 3-D characterization of nonconvex, irregular and interconnected particles can be used to more accurately quantify spatially-dependent parameters, such as tortuosity and pore-phase connectivity.

  7. Flexible carbon nanotube--Cu2O hybrid electrodes for li-ion batteries.

    Science.gov (United States)

    Goyal, Anubha; Reddy, Arava L M; Ajayan, Pulickel M

    2011-06-20

    This study demonstrates the formation of a flexible and free-standing carbon nanotube-copper oxide-poly(vinylidene fluoride) (CNT-Cu(2) O-PVDF) nanocomposite and its application as an electrode-separator material for Li-ion batteries. Binder-free hybrid electrodes are obtained by conformally coating CNTs with Cu(2) O via electrodeposition and then embedding the resulting architecture into a porous poly(vinylidene fluoride-hexafluoropropylene) PVDF-HFP-SiO(2) polymer electrolyte membrane. The synergistic presence of high-capacity transition metal oxides and conductive CNTs results in twice the reversible areal capacity of 2.3 mAh cm(-2) as compared to 1.2 mAh cm(-2) for pure CNTs.

  8. Virus-Assembled Flexible Electrode-Electrolyte Interfaces for Enhanced Polymer-Based Battery Applications

    Directory of Open Access Journals (Sweden)

    Ayan Ghosh

    2012-01-01

    Full Text Available High-aspect-ratio cobalt-oxide-coated Tobacco mosaic virus (TMV- assembled polytetrafluoroethylene (PTFE nonstick surfaces were integrated with a solvent-free polymer electrolyte to create an anode-electrolyte interface for use in lithium-ion batteries. The virus-assembled PTFE surfaces consisted primarily of cobalt oxide and were readily intercalated with a low-molecular-weight poly (ethylene oxide (PEO based diblock copolymer electrolyte to produce a solid anode-electrolyte system. The resulting polymer-coated virus-based system was then peeled from the PTFE backing to produce a flexible electrode-electrolyte component. Electrochemical studies indicated the virus-structured metal-oxide PEO-based interface was stable and displayed robust charge transfer kinetics. Combined, these studies demonstrate the development of a novel solid-state electrode architecture with a unique peelable and flexible processing attribute.

  9. On the use of transition metal oxysalts as conversion electrodes in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Aragon, Maria Jose; Leon, Bernardo; Perez Vicente, Carlos; Tirado, Jose L. [Laboratorio de Quimica Inorganica, Universidad de Cordoba, Edificio C3, Campus de Rabanales, 14071 Cordoba (Spain)

    2009-04-01

    Transition metal oxysalts are evaluated as conversion electrode material. Anhydrous iron oxalate is investigated and a comparison with manganese carbonate is carried out to envisage the possible extension of these studies to a vast number of transition metal oxysalts. The dehydration process is studied by thermal analysis to prepare the anhydrous oxysalts. Both manganese carbonate and iron oxalate are interesting candidates for the active material of the negative electrode of lithium-ion batteries. A higher reversible capacity and lower irreversible capacity are observed for the oxalate compound. The reversible capacity cannot be exclusively ascribed to redox processes involving iron. The low temperature synthesis of these materials makes them an inexpensive option for this purpose. (author)

  10. High performance electrodes in vanadium redox flow batteries through oxygen-enriched thermal activation

    Science.gov (United States)

    Pezeshki, Alan M.; Clement, Jason T.; Veith, Gabriel M.; Zawodzinski, Thomas A.; Mench, Matthew M.

    2015-10-01

    The roundtrip electrochemical energy efficiency is improved from 63% to 76% at a current density of 200 mA cm-2 in an all-vanadium redox flow battery (VRFB) by utilizing modified carbon paper electrodes in the high-performance no-gap design. Heat treatment of the carbon paper electrodes in a 42% oxygen/58% nitrogen atmosphere increases the electrochemically wetted surface area from 0.24 to 51.22 m2 g-1, resulting in a 100-140 mV decrease in activation overpotential at operationally relevant current densities. An enriched oxygen environment decreases the amount of treatment time required to achieve high surface area. The increased efficiency and greater depth of discharge doubles the total usable energy stored in a fixed amount of electrolyte during operation at 200 mA cm-2.

  11. B4C as a stable non-carbon-based oxygen electrode material for lithium-oxygen batteries

    Energy Technology Data Exchange (ETDEWEB)

    Song, Shidong; Xu, Wu; Cao, Ruiguo; Luo, Langli; Engelhard, Mark H.; Bowden, Mark E.; Liu, Bin; Estevez, Luis; Wang, Chong-Min; Zhang, Ji-Guang

    2017-01-19

    Lithium-oxygen (Li-O2) batteries have extremely high theoretical specific capacities and energy densities when compared with Li-ion batteries. However, the instability of both electrolyte and carbon-based oxygen electrode related to the nucleophilic attack of reduced oxygen species during oxygen reduction reaction and the electrochemical oxidation during oxygen evolution reaction are recognized as the major challenges in this field. Here we report the application of boron carbide (B4C) as the non-carbon based oxygen electrode material for aprotic Li-O2 batteries. B4C has high resistance to chemical attack, good conductivity, excellent catalytic activity and low density that are suitable for battery applications. The electrochemical activity and chemical stability of B4C are systematically investigated in aprotic electrolyte. Li-O2 cells using B4C based air electrodes exhibit better cycling stability than those used TiC based air electrode in 1 M LiTf-Tetraglyme electrolyte. The degradation of B4C based electrode is mainly due to be the loss of active sites on B4C electrode during cycles as identified by the structure and composition characterizations. These results clearly demonstrate that B4C is a very promising alternative oxygen electrode material for aprotic Li-O2 batteries. It can also be used as a standard electrode to investigate the stability of electrolytes.

  12. A multiscale description of the electronic transport within the hierarchical architecture of a composite electrode for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Badot, Jean-Claude [Laboratoire de Chimie de la Matiere Condensee de Paris ENSCP, CNRS Paris Cedex 5, (France); Ligneel, Enc; Guyomard, Dominigve; Lestriez, Bernard [Institut des Materiaux Jean Rouxel (IMN) Universite de Nantes, CNRS, Nantes (France); Dubrunfaut, Olivier [Laboratoire de Genie Electrique de Paris, SUPELEC Univ. Paris 06, University Paris-Sud, CNRS, Gif-sur-Yvette (France)

    2009-09-09

    The broadband dielectric spectroscopy technique is applied, for the first time, to a composite material used as an electrode for lithium battery. The electrical properties (permittivity and conductivity) are measured from low (a few Hz) to microwave (a few GHz) frequencies. The results demonstrate that the broadband dielectric spectroscopy technique is very sensitive to the different scales of the electrode architecture involved in electronic transport, from interatomic distances to macroscopic sizes, as well as to the morphology at these scales, coarse or fine distribution of the constituents. This work opens up new prospects for a more fundamental understanding and more rational optimization of the electronic transport in composite electrodes for lithium batteries and other electrochemical energy storage technologies (including other batteries, supercapacitors, low- and medium-temperature fuel cells), electrochemical sensors and conductor-insulator composite materials. (Abstract Copyright [2009], Wiley Periodicals, Inc.)

  13. Current-induced transition from particle-by-particle to concurrent intercalation in phase-separating battery electrodes

    KAUST Repository

    Li, Yiyang

    2014-09-14

    ©2014 Macmillan Publishers Limited. All rights reserved. Many battery electrodes contain ensembles of nanoparticles that phase-separate on (de)intercalation. In such electrodes, the fraction of actively intercalating particles directly impacts cycle life: a vanishing population concentrates the current in a small number of particles, leading to current hotspots. Reports of the active particle population in the phase-separating electrode lithium iron phosphate (LiFePO 4; LFP) vary widely, ranging from near 0% (particle-by-particle) to 100% (concurrent intercalation). Using synchrotron-based X-ray microscopy, we probed the individual state-of-charge for over 3,000 LFP particles. We observed that the active population depends strongly on the cycling current, exhibiting particle-by-particle-like behaviour at low rates and increasingly concurrent behaviour at high rates, consistent with our phase-field porous electrode simulations. Contrary to intuition, the current density, or current per active internal surface area, is nearly invariant with the global electrode cycling rate. Rather, the electrode accommodates higher current by increasing the active particle population. This behaviour results from thermodynamic transformation barriers in LFP, and such a phenomenon probably extends to other phase-separating battery materials. We propose that modifying the transformation barrier and exchange current density can increase the active population and thus the current homogeneity. This could introduce new paradigms to enhance the cycle life of phase-separating battery electrodes.

  14. The reaction current distribution in battery electrode materials revealed by XPS-based state-of-charge mapping.

    Science.gov (United States)

    Pearse, Alexander J; Gillette, Eleanor; Lee, Sang Bok; Rubloff, Gary W

    2016-07-28

    Morphologically complex electrochemical systems such as composite or nanostructured lithium ion battery electrodes exhibit spatially inhomogeneous internal current distributions, particularly when driven at high total currents, due to resistances in the electrodes and electrolyte, distributions of diffusion path lengths, and nonlinear current-voltage characteristics. Measuring and controlling these distributions is interesting from both an engineering standpoint, as nonhomogenous currents lead to lower utilization of electrode material, as well as from a fundamental standpoint, as comparisons between theory and experiment are relatively scarce. Here we describe a new approach using a deliberately simple model battery electrode to examine the current distribution in a electrode material limited by poor electronic conductivity. We utilize quantitative spatially resolved X-ray photoelectron spectroscopy to measure the spatial distribution of the state-of-charge of a V2O5 model electrode as a proxy measure for the current distribution on electrodes discharged at varying current densities. We show that the current at the electrode-electrolyte interface falls off with distance from the current collector, and that the current distribution is a strong function of total current. We compare the observed distributions with a simple analytical model which reproduces the dependence of the distribution on total current, but fails to predict the correct length scale. A more complete numerical simulation suggests that dynamic changes in the electronic conductivity of the V2O5 concurrent with lithium insertion may contribute to the differences between theory and experiment. Our observations should help inform design criteria for future electrode architectures.

  15. Environmentally-friendly aqueous Li (or Na)-ion battery with fast electrode kinetics and super-long life

    OpenAIRE

    Dong, Xiaoli; Chen, Long; Liu, Jingyuan; Haller, Servane; Wang, Yonggang; Xia, Yongyao

    2016-01-01

    Current rechargeable batteries generally display limited cycle life and slow electrode kinetics and contain environmentally unfriendly components. Furthermore, their operation depends on the redox reactions of metal elements. We present an original battery system that depends on the redox of I−/I3 − couple in liquid cathode and the reversible enolization in polyimide anode, accompanied by Li+ (or Na+) diffusion between cathode and anode through a Li+/Na+ exchange polymer membrane. There are n...

  16. Harvesting Energy from Salinity Differences Using Battery Electrodes in a Concentration Flow Cell.

    Science.gov (United States)

    Kim, Taeyoung; Rahimi, Mohammad; Logan, Bruce E; Gorski, Christopher A

    2016-09-06

    Salinity-gradient energy (SGE) technologies produce carbon-neutral and renewable electricity from salinity differences between seawater and freshwater. Capacitive mixing (CapMix) is a promising class of SGE technologies that captures energy using capacitive or battery electrodes, but CapMix devices have produced relatively low power densities and often require expensive materials. Here, we combined existing CapMix approaches to develop a concentration flow cell that can overcome these limitations. In this system, two identical battery (i.e., faradaic) electrodes composed of copper hexacyanoferrate (CuHCF) were simultaneously exposed to either high (0.513 M) or low (0.017 M) concentration NaCl solutions in channels separated by a filtration membrane. The average power density produced was 411 ± 14 mW m(-2) (normalized to membrane area), which was twice as high as previously reported values for CapMix devices. Power production was continuous (i.e., it did not require a charging period and did not vary during each step of a cycle) and was stable for 20 cycles of switching the solutions in each channel. The concentration flow cell only used inexpensive materials and did not require ion-selective membranes or precious metals. The results demonstrate that the concentration flow cell is a promising approach for efficiently harvesting energy from salinity differences.

  17. Mitigating mechanical failure of crystalline silicon electrodes for lithium batteries by morphological design.

    Science.gov (United States)

    An, Yonghao; Wood, Brandon C; Ye, Jianchao; Chiang, Yet-Ming; Wang, Y Morris; Tang, Ming; Jiang, Hanqing

    2015-07-21

    Although crystalline silicon (c-Si) anodes promise very high energy densities in Li-ion batteries, their practical use is complicated by amorphization, large volume expansion and severe plastic deformation upon lithium insertion. Recent experiments have revealed the existence of a sharp interface between crystalline Si (c-Si) and the amorphous LixSi alloy during lithiation, which propagates with a velocity that is orientation dependent; the resulting anisotropic swelling generates substantial strain concentrations that initiate cracks even in nanostructured Si. Here we describe a novel strategy to mitigate lithiation-induced fracture by using pristine c-Si structures with engineered anisometric morphologies that are deliberately designed to counteract the anisotropy in the crystalline/amorphous interface velocity. This produces a much more uniform volume expansion, significantly reducing strain concentration. Based on a new, validated methodology that improves previous models of anisotropic swelling of c-Si, we propose optimal morphological designs for c-Si pillars and particles. The advantages of the new morphologies are clearly demonstrated by mesoscale simulations and verified by experiments on engineered c-Si micropillars. The results of this study illustrate that morphological design is effective in improving the fracture resistance of micron-sized Si electrodes, which will facilitate their practical application in next-generation Li-ion batteries. The model and design approach present in this paper also have general implications for the study and mitigation of mechanical failure of electrode materials that undergo large anisotropic volume change upon ion insertion and extraction.

  18. Conductive Polymer-Coated VS4 Submicrospheres As Advanced Electrode Materials in Lithium-Ion Batteries.

    Science.gov (United States)

    Zhou, Yanli; Li, Yanlu; Yang, Jing; Tian, Jian; Xu, Huayun; Yang, Jian; Fan, Weiliu

    2016-07-27

    VS4 as an electrode material in lithium-ion batteries holds intriguing features like high content of sulfur and one-dimensional structure, inspiring the exploration in this field. Herein, VS4 submicrospheres have been synthesized via a simple solvothermal reaction. However, they quickly degrade upon cycling as an anode material in lithium-ion batteries. So, three conductive polymers, polythiophene (PEDOT), polypyrrole (PPY), and polyaniline (PANI), are coated on the surface to improve the electron conductivity, suppress the diffusion of polysulfides, and modify the interface between electrode/electrolyte. PANI is the best in the polymers. It improves the Coulombic efficiency to 86% for the first cycle and keeps the specific capacity at 755 mAh g(-1) after 50 cycles, higher than the cases of naked VS4 (100 mAh g(-1)), VS4@PEDOT (318 mAh g(-1)), and VS4@PPY (448 mAh g(-1)). The good performances could be attributed to the improved charge-transfer kinetics and the strong interaction between PANI and VS4 supported by theoretical simulation. The discharge voltage ∼2.0 V makes them promising cathode materials.

  19. Plasma processes in the preparation of lithium-ion battery electrodes and separators

    Science.gov (United States)

    Nava-Avendaño, J.; Veilleux, J.

    2017-04-01

    Lithium-ion batteries (LIBs) are the energy storage devices that dominate the portable electronic market. They are now also considered and used for electric vehicles and are foreseen to enable the smart grid. Preparing batteries with high energy and power densities, elevated cycleability and improved safety could be achieved by controlling the microstructure of the electrode materials and the interaction they have with the electrolyte over the working potential window. Selecting appropriate precursors, reducing the preparation steps and selecting more efficient synthesis methods could also significantly reduce the costs of LIB components. Implementing plasma technologies can represent a high capital investment, but the versatility of the technologies allows the preparation of powdered nanoparticles with different morphologies, as well as with carbon and metal oxide coatings. Plasma technologies can also enable the preparation of binder-free thin films and coatings for LIB electrodes, and the treatment of polymeric membranes to be used as separators. This review paper aims at highlighting the different thermal and non-thermal plasma technologies recently used to synthesize coated and non-coated active materials for LIB cathodes and anodes, and to modify the surface of separators.

  20. Flexible Paper Electrodes for Li-Ion Batteries Using Low Amount of TEMPO-Oxidized Cellulose Nanofibrils as Binder.

    Science.gov (United States)

    Lu, Huiran; Behm, Mårten; Leijonmarck, Simon; Lindbergh, Göran; Cornell, Ann

    2016-07-20

    Flexible Li-ion batteries attract increasing interest for applications in bendable and wearable electronic devices. TEMPO-oxidized cellulose nanofibrils (TOCNF), a renewable material, is a promising candidate as binder for flexible Li-ion batteries with good mechanical properties. Paper batteries can be produced using a water-based paper making process, avoiding the use of toxic solvents. In this work, finely dispersed TOCNF was used and showed good binding properties at concentrations as low as 4 wt %. The TOCNF was characterized using atomic force microscopy and found to be well dispersed with fibrils of average widths of about 2.7 nm and lengths of approximately 0.1-1 μm. Traces of moisture, trapped in the hygroscopic cellulose, is a concern when the material is used in Li-ion batteries. The low amount of binder reduces possible moisture and also increases the capacity of the electrodes, based on total weight. Effects of moisture on electrochemical battery performance were studied on electrodes dried at 110 °C in a vacuum for varying periods. It was found that increased drying time slightly increased the specific capacities of the LiFePO4 electrodes, whereas the capacities of the graphite electrodes decreased. The Coulombic efficiencies of the electrodes were not much affected by the varying drying times. Drying the electrodes for 1 h was enough to achieve good electrochemical performance. Addition of vinylene carbonate to the electrolyte had a positive effect on cycling for both graphite and LiFePO4. A failure mechanism observed at high TOCNF concentrations is the formation of compact films in the electrodes.

  1. Characterization of the 3-dimensional microstructure of a graphite negative electrode from a Li-ion battery

    DEFF Research Database (Denmark)

    Shearing, P.R.; Howard, L.E.; Jørgensen, Peter Stanley

    2010-01-01

    The 3-dimensional microstructure of a porous electrode from a lithium-ion battery has been characterized for the first time. We use X-ray tomography to reconstruct a 43 × 348 × 478 μm sample volume with voxel dimensions of 480 nm, subsequent division of the reconstructed volumes into sub-volumes ......The 3-dimensional microstructure of a porous electrode from a lithium-ion battery has been characterized for the first time. We use X-ray tomography to reconstruct a 43 × 348 × 478 μm sample volume with voxel dimensions of 480 nm, subsequent division of the reconstructed volumes into sub...

  2. Tunable Reaction Potentials in Open Framework Nanoparticle Battery Electrodes for Grid-Scale Energy Storage

    KAUST Repository

    Wessells, Colin D.

    2012-02-28

    The electrical energy grid has a growing need for energy storage to address short-term transients, frequency regulation, and load leveling. Though electrochemical energy storage devices such as batteries offer an attractive solution, current commercial battery technology cannot provide adequate power, and cycle life, and energy efficiency at a sufficiently low cost. Copper hexacyanoferrate and nickel hexacyanoferrate, two open framework materials with the Prussian Blue structure, were recently shown to offer ultralong cycle life and high-rate performance when operated as battery electrodes in safe, inexpensive aqueous sodium ion and potassium ion electrolytes. In this report, we demonstrate that the reaction potential of copper-nickel alloy hexacyanoferrate nanoparticles may be tuned by controlling the ratio of copper to nickel in these materials. X-ray diffraction, TEM energy dispersive X-ray spectroscopy, and galvanostatic electrochemical cycling of copper-nickel hexacyanoferrate reveal that copper and nickel form a fully miscible solution at particular sites in the framework without perturbing the structure. This allows copper-nickel hexacyanoferrate to reversibly intercalate sodium and potassium ions for over 2000 cycles with capacity retentions of 100% and 91%, respectively. The ability to precisely tune the reaction potential of copper-nickel hexacyanoferrate without sacrificing cycle life will allow the development of full cells that utilize the entire electrochemical stability window of aqueous sodium and potassium ion electrolytes. © 2012 American Chemical Society.

  3. Tunable reaction potentials in open framework nanoparticle battery electrodes for grid-scale energy storage.

    Science.gov (United States)

    Wessells, Colin D; McDowell, Matthew T; Peddada, Sandeep V; Pasta, Mauro; Huggins, Robert A; Cui, Yi

    2012-02-28

    The electrical energy grid has a growing need for energy storage to address short-term transients, frequency regulation, and load leveling. Though electrochemical energy storage devices such as batteries offer an attractive solution, current commercial battery technology cannot provide adequate power, and cycle life, and energy efficiency at a sufficiently low cost. Copper hexacyanoferrate and nickel hexacyanoferrate, two open framework materials with the Prussian Blue structure, were recently shown to offer ultralong cycle life and high-rate performance when operated as battery electrodes in safe, inexpensive aqueous sodium ion and potassium ion electrolytes. In this report, we demonstrate that the reaction potential of copper-nickel alloy hexacyanoferrate nanoparticles may be tuned by controlling the ratio of copper to nickel in these materials. X-ray diffraction, TEM energy dispersive X-ray spectroscopy, and galvanostatic electrochemical cycling of copper-nickel hexacyanoferrate reveal that copper and nickel form a fully miscible solution at particular sites in the framework without perturbing the structure. This allows copper-nickel hexacyanoferrate to reversibly intercalate sodium and potassium ions for over 2000 cycles with capacity retentions of 100% and 91%, respectively. The ability to precisely tune the reaction potential of copper-nickel hexacyanoferrate without sacrificing cycle life will allow the development of full cells that utilize the entire electrochemical stability window of aqueous sodium and potassium ion electrolytes.

  4. Synthesis and characterization of high performance electrode materials for lithium ion batteries

    Science.gov (United States)

    Hong, Jian

    Lithium-ion batteries have revolutionized portable electronics. Electrode reactions in these electrochemical systems are based on reversible intercalation of Li+ ions into the host electrode material with a concomitant addition/removal of electrons into the host. If such batteries are to find a wider market such as the automotive industry, less expensive and higher capacity electrode materials will be required. The olivine phase lithium iron phosphate has attracted the most attention because of its low cost and safety (high thermal and chemical stability). However, it is an intriguing fundamental problem to understand the fast electrochemical response from the poorly electronic conducting two-phase LiFePO4/FePO 4 system. This thesis focuses on determining the rate-limit step of LiFePO4. First, a LiFePO4 material, with vanadium substituting on the P-site, was synthesized, and found that the crystal structure change may cause high lithium diffusivity. Since an accurate Li diffusion coefficient cannot be measured by traditional electrochemical method in a three-electrode cell due to the phase transformation during measurement, a new method to measure the intrinsic electronic and ionic conductivity of mixed conductive LiFePO 4 was developed. This was based on the conductivity measurements of mixed conductive solid electrolyte using electrochemical impedance spectroscopy (EIS) and blocking electrode. The effects of ionic/electronic conductivity and phase transformation on the rate performance of LiFePO4 were also first investigated by EIS and other electrochemical technologies. Based on the above fundamental kinetics studies, an optimized LiFePO4 was used as a target to deposit 1mum LiFePO4 thin film at Oak Ridge National Laboratory using radio frequency (RF) magnetron sputtering. Similar to the carbon coated LiFePO4 powder electrode, the carbon-contained RF LiFePO4 film with no preferential orientation showed excellent capacity and rate capability both at 25°C and -20

  5. High rate capabilities Fe3O4-based Cu nano-architectured electrodes for lithium-ion battery applications.

    Science.gov (United States)

    Taberna, P L; Mitra, S; Poizot, P; Simon, P; Tarascon, J-M

    2006-07-01

    All battery technologies are known to suffer from kinetic problems linked to the solid-state diffusion of Li in intercalation electrodes, the conductivity of the electrolyte in some cases and the quality of interfaces. For Li-ion technology the latter effect is especially acute when conversion rather than intercalation electrodes are used. Nano-architectured electrodes are usually suggested to enhance kinetics, although their realization is cumbersome. To tackle this issue for the conversion electrode material Fe3O4, we have used a two-step electrode design consisting of the electrochemically assisted template growth of Cu nanorods onto a current collector followed by electrochemical plating of Fe3O4. Using such electrodes, we demonstrate a factor of six improvement in power density over planar electrodes while maintaining the same total discharge time. The capacity at the 8C rate was 80% of the total capacity and was sustained over 100 cycles. The origin of the large hysteresis between charge and discharge, intrinsic to conversion reactions, is discussed and approaches to reduce it are proposed. We hope that such findings will help pave the way for the use of conversion reaction electrodes in future-generation Li-ion batteries.

  6. Pie-like electrode design for high-energy density lithium-sulfur batteries

    Science.gov (United States)

    Li, Zhen; Zhang, Jin Tao; Chen, Yu Ming; Li, Ju; Lou, Xiong Wen (David)

    2015-11-01

    Owing to the overwhelming advantage in energy density, lithium-sulfur (Li-S) battery is a promising next-generation electrochemical energy storage system. Despite many efforts in pursuing long cycle life, relatively little emphasis has been placed on increasing the areal energy density. Herein, we have designed and developed a `pie' structured electrode, which provides an excellent balance between gravimetric and areal energy densities. Combining lotus root-like multichannel carbon nanofibers `filling' and amino-functionalized graphene `crust', the free-standing paper electrode (S mass loading: 3.6 mg cm-2) delivers high specific capacity of 1,314 mAh g-1 (4.7 mAh cm-2) at 0.1 C (0.6 mA cm-2) accompanied with good cycling stability. Moreover, the areal capacity can be further boosted to more than 8 mAh cm-2 by stacking three layers of paper electrodes with S mass loading of 10.8 mg cm-2.

  7. The negative electrode development for a Ni-MH battery prototype

    Energy Technology Data Exchange (ETDEWEB)

    Cuscueta, D.J., E-mail: cuscueta@cab.cnea.gov.a [Centro Atomico Bariloche-CNEA, Instituto Balseiro-UNCu, CONICET, Av. Bustillo 9500 (8400) San Carlos de Bariloche, R.N. (Argentina); Ghilarducci, A.A.; Salva, H.R. [Centro Atomico Bariloche-CNEA, Instituto Balseiro-UNCu, CONICET, Av. Bustillo 9500 (8400) San Carlos de Bariloche, R.N. (Argentina); Milocco, R.H. [Grupo Control Automatico y Sistemas (GCAyS), Depto. Electrotecnia, Facultad de Ingenieria, Universidad Nacional del Comahue, Buenos Aires 1400 (8300) Neuquen (Argentina); Castro, E.B. [Instituto de Investigaciones Fisicoquimicas Teoricas y Aplicadas (INIFTA) - Universidad Nacional La Plata. Suc 4, CC16 (1900), La Plata, Bs As (Argentina)

    2009-10-01

    The negative electrode development for a nickel-metal hydride battery (Ni-MH) prototype was performed with the following procedure: (1) the Lm{sub 0.95}Ni{sub 3.8}Co{sub 0.3}Mn{sub 0.3}Al{sub 0.4} (Lm=lanthanum rich mischmetal) intermetallic alloy was elaborated by melting the pure elements in an induction furnace inside a boron nitride crucible under an inert atmosphere, (2) the obtained alloy was crushed and sieved between 44 and 74 mum and mixed with teflonized carbon; (3) the compound was assembled together with a current collector and pressed in a cylindrical matrix. The obtained electrode presented a disc shape, with 11 mm diameter and approximately 1 mm thickness. The crystalline structure of the hydrogen storage alloy was examined using X-ray diffractometry. The measured hcp lattice volume was 1.78% larger than the precursor LaNi{sub 5} intermetallic alloy, increasing the available space for hydrogen movement. Energy dispersive spectroscopy (EDS) and scanning electronic microscopy (SEM) measurements were used before and after hydriding in order to verify the alloy sample homogeneity. The negative electrode was electrochemically tested by using a laboratory cell. It activates almost totally in its first cycle, which is an excellent characteristic from the commercial point of view. The maximum discharge capacity reached was 314.2 mA h/g in the 10th cycle.

  8. Heterogeneous WSx/WO₃ Thorn-Bush Nanofiber Electrodes for Sodium-Ion Batteries.

    Science.gov (United States)

    Ryu, Won-Hee; Wilson, Hope; Sohn, Sungwoo; Li, Jinyang; Tong, Xiao; Shaulsky, Evyatar; Schroers, Jan; Elimelech, Menachem; Taylor, André D

    2016-03-22

    Heterogeneous electrode materials with hierarchical architectures promise to enable considerable improvement in future energy storage devices. In this study, we report on a tailored synthetic strategy used to create heterogeneous tungsten sulfide/oxide core-shell nanofiber materials with vertically and randomly aligned thorn-bush features, and we evaluate them as potential anode materials for high-performance Na-ion batteries. The WSx (2 ≤ x ≤ 3, amorphous WS3 and crystalline WS2) nanofiber is successfully prepared by electrospinning and subsequent calcination in a reducing atmosphere. To prevent capacity degradation of the WSx anodes originating from sulfur dissolution, a facile post-thermal treatment in air is applied to form an oxide passivation surface. Interestingly, WO3 thorn bundles are randomly grown on the nanofiber stem, resulting from the surface conversion. We elucidate the evolving morphological and structural features of the nanofibers during post-thermal treatment. The heterogeneous thorn-bush nanofiber electrodes deliver a high second discharge capacity of 791 mAh g(-1) and improved cycle performance for 100 cycles compared to the pristine WSx nanofiber. We show that this hierarchical design is effective in reducing sulfur dissolution, as shown by cycling analysis with counter Na electrodes.

  9. Environmentally-friendly aqueous Li (or Na)-ion battery with fast electrode kinetics and super-long life.

    Science.gov (United States)

    Dong, Xiaoli; Chen, Long; Liu, Jingyuan; Haller, Servane; Wang, Yonggang; Xia, Yongyao

    2016-01-01

    Current rechargeable batteries generally display limited cycle life and slow electrode kinetics and contain environmentally unfriendly components. Furthermore, their operation depends on the redox reactions of metal elements. We present an original battery system that depends on the redox of I(-)/I3 (-) couple in liquid cathode and the reversible enolization in polyimide anode, accompanied by Li(+) (or Na(+)) diffusion between cathode and anode through a Li(+)/Na(+) exchange polymer membrane. There are no metal element-based redox reactions in this battery, and Li(+) (or Na(+)) is only used for charge transfer. Moreover, the components (electrolyte/electrode) of this system are environment-friendly. Both electrodes are demonstrated to have very fast kinetics, which gives the battery a supercapacitor-like high power. It can even be cycled 50,000 times when operated within the electrochemical window of 0 to 1.6 V. Such a system might shed light on the design of high-safety and low-cost batteries for grid-scale energy storage.

  10. A review of thermal performance improving methods of lithium ion battery: Electrode modification and thermal management system

    Science.gov (United States)

    Zhao, Rui; Zhang, Sijie; Liu, Jie; Gu, Junjie

    2015-12-01

    Lithium ion (Li-ion) battery has emerged as an important power source for portable devices and electric vehicles due to its superiority over other energy storage technologies. A mild temperature variation as well as a proper operating temperature range are essential for a Li-ion battery to perform soundly and have a long service life. In this review paper, the heat generation and dissipation of Li-ion battery are firstly analyzed based on the energy conservation equations, followed by an examination of the hazardous effects of an above normal operating temperature. Then, advanced techniques in respect of electrode modification and systematic battery thermal management are inspected in detail as solutions in terms of reducing internal heat production and accelerating external heat dissipation, respectively. Specifically, variable parameters like electrode thickness and particle size of active material, along with optimization methods such as coating, doping, and adding conductive media are discussed in the electrode modification section, while the current development in air cooling, liquid cooling, heat pipe cooling, and phase change material cooling systems are reviewed in the thermal management part as different ways to improve the thermal performance of Li-ion batteries.

  11. Binder-Free and Carbon-Free Nanoparticle Batteries: A Method for Nanoparticle Electrodes without Polymeric Binders or Carbon Black

    KAUST Repository

    Ha, Don-Hyung

    2012-10-10

    In this work, we have developed a new fabrication method for nanoparticle (NP) assemblies for Li-ion battery electrodes that require no additional support or conductive materials such as polymeric binders or carbon black. By eliminating these additives, we are able to improve the battery capacity/weight ratio. The NP film is formed by using electrophoretic deposition (EPD) of colloidally synthesized, monodisperse cobalt NPs that are transformed through the nanoscale Kirkendall effect into hollow Co 3O 4. EPD forms a network of NPs that are mechanically very robust and electrically connected, enabling them to act as the Li-ion battery anode. The morphology change through cycles indicates stable 5-10 nm NPs form after the first lithiation remained throughout the cycling process. This NP-film battery made without binders and conductive additives shows high gravimetric (>830 mAh/g) and volumetric capacities (>2100 mAh/cm 3) even after 50 cycles. Because similar films made from drop-casting do not perform well under equal conditions, EPD is seen as the critical step to create good contacts between the particles and electrodes resulting in this significant improvement in battery electrode assembly. This is a promising system for colloidal nanoparticles and a template for investigating the mechanism of lithiation and delithiation of NPs. © 2012 American Chemical Society.

  12. Electrode property of single-walled carbon nanotubes in all-solid-state lithium ion battery using polymer electrolyte

    Science.gov (United States)

    Sakamoto, Y.; Ishii, Y.; Kawasaki, S.

    2016-07-01

    Electrode properties of single-walled carbon nanotubes (SWCNTs) in an all-solid-state lithium ion battery were investigated using poly-ethylene oxide (PEO) solid electrolyte. Charge-discharge curves of SWCNTs in the solid electrolyte cell were successfully observed. It was found that PEO electrolyte decomposes on the surface of SWCNTs.

  13. Metal hydride-based materials towards high performance negative electrodes for all-solid-state lithium-ion batteries.

    Science.gov (United States)

    Zeng, Liang; Kawahito, Koji; Ikeda, Suguru; Ichikawa, Takayuki; Miyaoka, Hiroki; Kojima, Yoshitsugu

    2015-06-18

    Electrode performances of MgH2-LiBH4 composite materials for lithium-ion batteries have been studied using LiBH4 as the solid-state electrolyte, which shows a high reversible capacity of 1650 mA h g(-1) with an extremely low polarization of 0.05 V, durable cyclability and robust rate capability.

  14. Investigation of electrolyte wetting in lithium ion batteries: Effects of electrode pore structures and solution

    Science.gov (United States)

    Sheng, Yangping

    Beside natural source energy carriers such as petroleum, coal and natural gas, the lithium ion battery is a promising man-made energy carrier for the future. This is a similar process evolved from horse-powered era to engine driven age. There are still a lot of challenges ahead like low energy density, low rate performance, aging problems, high cost and safety etc. In lithium ion batteries, investigation about manufacturing process is as important as the development of material. The manufacturing of lithium ion battery, including production process (slurry making, coating, drying etc.), and post-production (slitting, calendering etc.) is also complicated and critical to the overall performance of the battery. It includes matching the capacity of anode and cathode materials, trial-and-error investigation of thickness, porosity, active material and additive loading, detailed microscopic models to understand, optimize, and design these systems by changing one or a few parameters at a time. In the manufacturing, one of the most important principles is to ensure good wetting properties between porous solid electrodes and liquid electrolyte. Besides the material surface properties, it is the process of electrolyte transporting to fill the pores in the electrode after injection is less noticed in academic, where only 2-3 drops of electrolyte are needed for lab coin cell level. In industry, the importance of electrolyte transport is well known and it is considered as part of electrolyte wetting (or initial wetting in some situations). In consideration of practical usage term, electrolyte wetting is adopted to use in this dissertation for electrolyte transporting process, although the surface chemistry about wetting is not covered. An in-depth investigation about electrolyte wetting is still missing, although it has significant effects in manufacturing. The electrolyte wetting is determined by properties of electrolyte and electrode microstructure. Currently, only viscosity

  15. In Situ Radiographic Investigation of (De)Lithiation Mechanisms in a Tin-Electrode Lithium-Ion Battery.

    Science.gov (United States)

    Sun, Fu; Markötter, Henning; Zhou, Dong; Alrwashdeh, Saad Sabe Sulaiman; Hilger, Andre; Kardjilov, Nikolay; Manke, Ingo; Banhart, John

    2016-05-10

    The lithiation and delithiation mechanisms of multiple-Sn particles in a customized flat radiography cell were investigated by in situ synchrotron radiography. For the first time, four (de)lithiation phenomena in a Sn-electrode battery system are highlighted: 1) the (de)lithiation behavior varies between different Sn particles, 2) the time required to lithiate individual Sn particles is markedly different from the time needed to discharge the complete battery, 3) electrochemical deactivation of originally electrochemically active particles is reported, and 4) a change of electrochemical behavior of individual particles during cycling is found and explained by dynamic changes of (de)lithiation pathways amongst particles within the electrode. These unexpected findings fundamentaly expand the understanding of the underlying (de)lithiation mechanisms inside commercial lithium-ion batteries (LIBs) and would open new design principles for high-performance next-generation LIBs.

  16. Quantification of preferred orientation in graphite electrodes for Li-ion batteries with a novel X-ray-diffraction-based method

    Science.gov (United States)

    Malifarge, Simon; Delobel, Bruno; Delacourt, Charles

    2017-03-01

    To answer the demand of increased autonomy in transportation applications, the energy density of battery electrode need to be enhanced. The porous electrode microstructure needs to be controlled to optimize battery performance and prevent electrode degradation (e.g., Li plating). Graphite negative electrodes generally consist of anisotropic particles that exhibit a preferred orientation. Graphite particles tend to stack perpendicular to ionic pathways which results in transport issues and reduces overall battery power capability. In this context, a method based on X-ray diffraction is described to quantify the preferred orientation of graphite particles in actual electrodes. A step orientation-distribution function is used to describe the pole-density profile of the diffracting graphite crystallites. A fraction of graphite particles oriented parallel to the electrode current collector within a tilt tolerance is derived from the step function. An application of this method is presented on a set of graphite electrodes that underwent different calendering conditions.

  17. Method for producing La/Ce/MM/Y base alloys, resulting alloys and battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Gschneidner, Jr., Karl A.; Schmidt, Frederick A.

    2016-12-20

    A carbothermic reduction method is provided for reducing a La-, Ce-, MM-, and/or Y-containing oxide in the presence of carbon and a source of a reactant element comprising Si, Ge, Sn, Pb, As, Sb, Bi, and/or P to form an intermediate alloy material including a majority of La, Ce, MM, and/or Y and a minor amount of the reactant element. The intermediate material is useful as a master alloy for in making negative electrode materials for a metal hydride battery, as hydrogen storage alloys, as master alloy additive for addition to a melt of commercial Mg and Al alloys, steels, cast irons, and superalloys; or in reducing Sm.sub.2O.sub.3 to Sm metal for use in Sm--Co permanent magnets.

  18. Experimental and theoretical investigations of functionalized boron nitride as electrode materials for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Fan; Nemeth, Karoly; Bareño, Javier; Dogan, Fulya; Bloom, Ira D.; Shaw, Leon L.

    2016-01-01

    The feasibility of synthesizing functionalized h-BN (FBN) via the reaction between molten LiOH and solid h-BN is studied for the first time and its first ever application as an electrode material in Li-ion batteries is evaluated. Density functional theory (DFT) calculations are performed to provide mechanistic understanding of the possible electrochemical reactions derived from the FBN. Various materials characterizations reveal that the melt-solid reaction can lead to exfoliation and functionalization of h-BN simultaneously, while electrochemical analysis proves that the FBN can reversibly store charges through surface redox reactions with good cycle stability and coulombic efficiency. DFT calculations have provided physical insights into the observed electrochemical properties derived from the FBN.

  19. Metal hydrides used as negative electrode materials for Li-ion batteries

    Science.gov (United States)

    Sartori, Sabrina; Cuevas, Fermin; Latroche, Michel

    2016-02-01

    Energy is a key issue for future generation. Researches are conducted worldwide to develop new efficient means for energy conversion and storage. Electrochemical storage is foreseen as an efficient way to handle intermittent renewable energy production. The most advanced batteries are nowadays based on lithium-ion technology though their specific capacities should be significantly increased to bring solution to mass storage. Conversion reactions are one way to step forward larger capacities at the anode. We here review the possibility to use metallic or complex hydrides as negative electrode using conversion reaction of hydride with lithium. Moreover, promising alloying of lithium with the metallic species might provide additional reversible capacities. Both binary and ternary systems are reviewed and results are compared in the frame of the electrochemical application.

  20. Hydrogen evolution at the negative electrode of the all-vanadium redox flow batteries

    Science.gov (United States)

    Sun, Che-Nan; Delnick, Frank M.; Baggetto, Loïc; Veith, Gabriel M.; Zawodzinski, Thomas A.

    2014-02-01

    This work demonstrates a quantitative method to determine the hydrogen evolution rate occurring at the negative carbon electrode of the all vanadium redox flow battery (VRFB). Two carbon papers examined by buoyancy measurements yield distinct hydrogen formation rates (0.170 and 0.005 μmol min-1 g-1). The carbon papers have been characterized using electron microscopy, nitrogen gas adsorption, capacitance measurement by electrochemical impedance spectroscopy (EIS), and X-ray photoelectron spectroscopy (XPS). We find that the specific electrochemical surface area (ECSA) of the carbon material has a strong influence on the hydrogen generation rate. This is discussed in light of the use of high surface area material to obtain high reaction rates in the VRFB.

  1. S-functionalized MXenes as electrode materials for Li-ion batteries

    KAUST Repository

    Zhu, Jiajie

    2016-09-03

    MXenes are promising electrode materials for Li-ion batteries because of their high Li capacities and cycling rates. We use density functional theory to investigate the structural and energy storage properties of Li decorated Zr2C and Zr2CX2 (X = F, O and S). We find for Zr2C and Zr2CS2 high Li specific capacities and low diffusion barriers. To overcome the critical drawbacks of the OH, F, and O groups introduced during the synthesis we propose substitution by S groups and demonstrate that an exchange reaction is indeed possible. Zr2CS2 shows a similar Li specific capacity as Zr2CO2 but a substantially reduced diffusion barrier. © 2016 Elsevier Ltd

  2. Atomic-scale structure evolution in a quasi-equilibrated electrochemical process of electrode materials for rechargeable batteries.

    Science.gov (United States)

    Gu, Lin; Xiao, Dongdong; Hu, Yong-Sheng; Li, Hong; Ikuhara, Yuichi

    2015-04-01

    Lithium-ion batteries have proven to be extremely attractive candidates for applications in portable electronics, electric vehicles, and smart grid in terms of energy density, power density, and service life. Further performance optimization to satisfy ever-increasing demands on energy storage of such applications is highly desired. In most of cases, the kinetics and stability of electrode materials are strongly correlated to the transport and storage behaviors of lithium ions in the lattice of the host. Therefore, information about structural evolution of electrode materials at an atomic scale is always helpful to explain the electrochemical performances of batteries at a macroscale. The annular-bright-field (ABF) imaging in aberration-corrected scanning transmission electron microscopy (STEM) allows simultaneous imaging of light and heavy elements, providing an unprecedented opportunity to probe the nearly equilibrated local structure of electrode materials after electrochemical cycling at atomic resolution. Recent progress toward unraveling the atomic-scale structure of selected electrode materials with different charge and/or discharge state to extend the current understanding of electrochemical reaction mechanism with the ABF and high angle annular dark field STEM imaging is presented here. Future research on the relationship between atomic-level structure evolution and microscopic reaction mechanisms of electrode materials for rechargeable batteries is envisaged.

  3. Nickel Hexacyanoferrate Nanoparticle Electrodes For Aqueous Sodium and Potassium Ion Batteries

    KAUST Repository

    Wessells, Colin D.

    2011-12-14

    The electrical power grid faces a growing need for large-scale energy storage over a wide range of time scales due to costly short-term transients, frequency regulation, and load balancing. The durability, high power, energy efficiency, and low cost needed for grid-scale storage pose substantial challenges for conventional battery technology.(1, 2)Here, we demonstrate insertion/extraction of sodium and potassium ions in a low-strain nickel hexacyanoferrate electrode material for at least five thousand deep cycles at high current densities in inexpensive aqueous electrolytes. Its open-framework structure allows retention of 66% of the initial capacity even at a very high (41.7C) rate. At low current densities, its round trip energy efficiency reaches 99%. This low-cost material is readily synthesized in bulk quantities. The long cycle life, high power, good energy efficiency, safety, and inexpensive production method make nickel hexacyanoferrate an attractive candidate for use in large-scale batteries to support the electrical grid. © 2011 American Chemical Society.

  4. Carbon−Silicon Core−Shell Nanowires as High Capacity Electrode for Lithium Ion Batteries

    KAUST Repository

    Cui, Li-Feng

    2009-09-09

    We introduce a novel design of carbon-silicon core-shell nanowires for high power and long life lithium battery electrodes. Amorphous silicon was coated onto carbon nanofibers to form a core-shell structure and the resulted core-shell nanowires showed great performance as anode material. Since carbon has a much smaller capacity compared to silicon, the carbon core experiences less structural stress or damage during lithium cycling and can function as a mechanical support and an efficient electron conducting pathway. These nanowires have a high charge storage capacity of ∼2000 mAh/g and good cycling life. They also have a high Coulmbic efficiency of 90% for the first cycle and 98-99.6% for the following cycles. A full cell composed of LiCoO2 cathode and carbon-silicon core-shell nanowire anode is also demonstrated. Significantly, using these core-shell nanowires we have obtained high mass loading and an area capacity of ∼4 mAh/cm2, which is comparable to commercial battery values. © 2009 American Chemical Society.

  5. Crystalline-Amorphous Core−Shell Silicon Nanowires for High Capacity and High Current Battery Electrodes

    KAUST Repository

    Cui, Li-Feng

    2009-01-14

    Silicon is an attractive alloy-type anode material for lithium ion batteries because of its highest known capacity (4200 mAh/g). However silicon\\'s large volume change upon lithium insertion and extraction, which causes pulverization and capacity fading, has limited its applications. Designing nanoscale hierarchical structures is a novel approach to address the issues associated with the large volume changes. In this letter, we introduce a core-shell design of silicon nanowires for highpower and long-life lithium battery electrodes. Silicon crystalline- amorphous core-shell nanowires were grown directly on stainless steel current collectors by a simple one-step synthesis. Amorphous Si shells instead of crystalline Si cores can be selected to be electrochemically active due to the difference of their lithiation potentials. Therefore, crystalline Si cores function as a stable mechanical support and an efficient electrical conducting pathway while amorphous shells store Li ions. We demonstrate here that these core-shell nanowires have high charge storage capacity (̃1000 mAh/g, 3 times of carbon) with ̃90% capacity retention over 100 cycles. They also show excellent electrochemical performance at high rate charging and discharging (6.8 A/g, ̃20 times of carbon at 1 h rate). © 2009 American Chemical Society.

  6. NMR study of electrode materials for lithium ion-batteries; Etude par RMN de materiaux d'electrode pour batteries lithium-ion

    Energy Technology Data Exchange (ETDEWEB)

    Chazel, C.

    2006-01-15

    This work is devoted to the study of LiMO{sub 2} et LiM{sub 2}O{sub 4} (M: transition metal) intercalation compounds used as electrode material for lithium-ion batteries. Solid state NMR allows one to characterise the local environment of the lithium ions present in these phases by the use of the hyperfine interactions due to the presence of some electron spin density coming from localised electrons (Fermi-contact shift) or itinerant electrons (Knight shift) on the lithium nucleus. By following the transformation of the LiNiO{sub 2} layered phase into the LiNi{sub 2}O{sub 4} spinel material using lithium NMR, we studied the nature of the asymmetric signal observed for LiNiO{sub 2}, and the influence of the departure from the ideal stoichiometry; we showed a coupled ion/electron hopping in Li{sub X}NiO{sub 2} phases linked to Li/vacancy and Ni{sup 3+}/Ni{sup 4+} ordering, and finally showed the existence of structural defects within the LiNi{sub 2}O{sub 4} spinel phase obtained by thermal treatment of Li{sub 0.5}NiO{sub 2}. Lithium NMR of the intercalated materials obtained from the LiTi{sub 2}O{sub 4} and Li{sub 4}Ti{sub 5}O{sub 12} spinels showed a metallic behaviour for Li{sub 2}Ti{sub 2}O{sub 4} with a Knight shift of the NMR signal similar to that of LiTi{sub 2}O{sub 4}, and signals intermediate in nature between Knight and Fermi-contact shifts for Li{sub 7}Ti{sub 5}O{sub 12}. (author)

  7. Copper hexacyanoferrate battery electrodes with long cycle life and high power

    KAUST Repository

    Wessells, Colin D.

    2011-11-22

    Short-term transients, including those related to wind and solar sources, present challenges to the electrical grid. Stationary energy storage systems that can operate for many cycles, at high power, with high round-trip energy efficiency, and at low cost are required. Existing energy storage technologies cannot satisfy these requirements. Here we show that crystalline nanoparticles of copper hexacyanoferrate, which has an ultra-low strain open framework structure, can be operated as a battery electrode in inexpensive aqueous electrolytes. After 40,000 deep discharge cycles at a 17g-C rate, 83% of the original capacity of copper hexacyanoferrate is retained. Even at a very high cycling rate of 83g-C, two thirds of its maximum discharge capacity is observed. At modest current densities, round-trip energy efficiencies of 99% can be achieved. The low-cost, scalable, room-temperature co-precipitation synthesis and excellent electrode performance of copper hexacyanoferrate make it attractive for large-scale energy storage systems. © 2011 Macmillan Publishers Limited. All rights reserved.

  8. Pyrometallurgical Extraction of Valuable Elements in Ni-Metal Hydride Battery Electrode Materials

    Science.gov (United States)

    Jiang, Yin-ju; Deng, Yong-chun; Bu, Wen-gang

    2015-10-01

    Gas selective reduction-oxidation (redox) and melting separation were consecutively applied to electrode materials of AB5-type Ni-metal hydride batteries leading to the production of a Ni-Co alloy and slag enriched with rare earth oxides (REO). In the selective redox process, electrode materials were treated with H2/H2O at 1073 K and 1173 K (800 °C and 900 °C). Active elements such as REs, Al, and Mn were oxidized whereas relatively inert elements such as Ni and Co were transformed into their elemental states in the treated materials. SiO2 and Al2O3 powders were added into the treated materials as fluxes which were then melted at 1823 K (1550 °C) to yield a Ni-Co alloy and a REO-SiO2-Al2O3-MnO slag. The high-purity Ni-Co alloy produced can be used as a raw material for AB5-type hydrogen-storage alloy. The REO content in slag was very high, i.e., 48.51 pct, therefore it can be used to recycle rare earth oxides.

  9. Manufacturing of advanced Li(NiMnCo)O2 electrodes for lithium-ion batteries

    Science.gov (United States)

    Smyrek, P.; Pröll, J.; Rakebrandt, J.-H.; Seifert, H. J.; Pfleging, W.

    2015-03-01

    Lithium-ion batteries require an increase in cell life-time as well as an improvement in cycle stability in order to be used as energy storage systems, e.g. for stationary devices or electric vehicles. Nowadays, several cathode materials such as Li(NiMnCo)O2 (NMC) are under intense investigation to enhanced cell cycling behavior by simultaneously providing reasonable costs. Previous studies have shown that processing of three-dimensional (3D) micro-features in electrodes using nanosecond laser radiation further increases the active surface area and therefore, the lithium-ion diffusion cell kinetics. Within this study, NMC cathodes were prepared by tape-casting and laser-structured using nanosecond laser radiation. Furthermore, laser-induced breakdown spectroscopy (LIBS) was used in a first experimental attempt to analyze the lithium distribution in unstructured NMC cathodes at different state-of-charges (SOC). LIBS will be applied to laser-structured cathodes in order to investigate the lithium distribution at different SOC. The results will be compared to those obtained for unstructured electrodes to examine advantages of 3D micro-structures with respect to lithium-ion diffusion kinetics.

  10. Electrospun FeS2@Carbon Fiber Electrode as a High Energy Density Cathode for Rechargeable Lithium Batteries.

    Science.gov (United States)

    Zhu, Yujie; Fan, Xiulin; Suo, Liumin; Luo, Chao; Gao, Tao; Wang, Chunsheng

    2016-01-26

    In this study, an FeS2@carbon fiber electrode is developed with FeS2 nanoparticles either embedded in or attached to carbon fibers by using an electrospinning method. By applying this binder-free, metal-current-collector-free FeS2@carbon fiber electrode, both the redox reaction and capacity decay mechanisms for the Li-FeS2 system are revealed by changing the electrolyte (conventional carbonate electrolyte and a "solvent-in-salt"-type Li-S battery electrolyte) and working voltage ranges (1.0-3.0 V and 1.5-3.0 V vs Li/Li(+)). The FeS2@carbon fiber electrode shows stable cycling performance in both the conventional carbonate electrolyte and the solvent-in-salt-type Li-S battery electrolyte in the voltage range of 1.5-3.0 V. Electrochemical tests in the solvent-in-salt-type Li-S battery electrolyte indicate that the Li-FeS2 system becomes a hybrid of the Li-S cell and Li-iron sulfide cell after the initial cycle. Based on the understanding on the capacity decay mechanisms, the cycling stability of the Li-FeS2 system in the voltage range of 1.0-3.0 V is then significantly enhanced by coating the FeS2@carbon fiber electrode with a thin layer of Al2O3. The Al2O3-coated electrode demonstrates excellent cycling performance with high discharge energy densities at both the material level (∼1300 Wh/kg-FeS2) and the electrode level (∼1000 Wh/kg-FeS2 electrode).

  11. Liquid-Metal Electrode to Enable Ultra-Low Temperature Sodium-Beta Alumina Batteries for Renewable Energy Storage

    Energy Technology Data Exchange (ETDEWEB)

    Lu, Xiaochuan; Li, Guosheng; Kim, Jin Yong; Mei, Donghai; Lemmon, John P.; Sprenkle, Vincent L.; Liu, Jun

    2014-08-01

    Metal electrodes have a high capacity for energy storage but have found limited applications in batteries because of dendrite formation and other problems. In this paper, we report a new alloying strategy that can significantly reduce the melting temperature and improve wetting with the electrolyte to allow the use of liquid metal as anode in sodium-beta alumina batteries (NBBs) at much lower temperatures (e.g., 95 to 175°C). Commercial NBBs such as sodium-sulfur (Na-S) battery and sodium-metal halide (ZEBRA) batteries typically operate at relatively high temperatures (e.g., 300-350°C) due to poor wettability of sodium on the surface of β"-Al2O3. Our combined experimental and computational studies suggest that Na-Cs alloy can replace pure sodium as the anode material, which provides a significant improvement in wettability, particularly at lower temperatures (i.e., <200°C). Single cells with the Na-Cs alloy anode exhibit excellent cycling life over those with pure sodium anode at 175 and 150°C. The cells can even operate at 95°C, which is below the melting temperature of pure sodium. These results demonstrate that NBB can be operated at ultra lower temperatures with successfully solving the wetting issue. This work also suggests a new strategy to use liquid metal as the electrode materials for advanced batteries that can avoid the intrinsic safety issues associated with dendrite formation on the anode.

  12. Phase Boundary Propagation in Li-Alloying Battery Electrodes Revealed by Liquid-Cell Transmission Electron Microscopy.

    Science.gov (United States)

    Leenheer, Andrew J; Jungjohann, Katherine L; Zavadil, Kevin R; Harris, Charles T

    2016-06-28

    Battery cycle life is directly influenced by the microstructural changes occurring in the electrodes during charge and discharge cycles. Here, we image in situ the nanoscale phase evolution in negative electrode materials for Li-ion batteries using a fully enclosed liquid cell in a transmission electron microscope (TEM) to reveal early degradation that is not evident in the charge-discharge curves. To compare the electrochemical phase transformation behavior between three model materials, thin films of amorphous Si, crystalline Al, and crystalline Au were lithiated and delithiated at controlled rates while immersed in a commercial liquid electrolyte. This method allowed for the direct observation of lithiation mechanisms in nanoscale negative electrodes, revealing that a simplistic model of a surface-to-interior lithiation front is insufficient. For the crystalline films, a lithiation front spread laterally from a few initial nucleation points, with continued grain nucleation along the growing interface. The intermediate lithiated phases were identified using electron diffraction, and high-resolution postmortem imaging revealed the details of the final microstructure. Our results show that electrochemically induced solid-solid phase transformations can lead to highly concentrated stresses at the laterally propagating phase boundary which should be considered for future designs of nanostructured electrodes for Li-ion batteries.

  13. PbO2-modified graphite felt as the positive electrode for an all-vanadium redox flow battery

    Science.gov (United States)

    Wu, Xiaoxin; Xu, Hongfeng; Lu, Lu; Zhao, Hong; Fu, Jie; Shen, Yang; Xu, Pengcheng; Dong, Yiming

    2014-03-01

    A novel approach for enhancing the electrochemical performance of graphite felt electrodes by employing non-precious metal oxides is designed for an all-vanadium redox flow battery (VRFB). Lead dioxide (PbO2) is prepared through pulse electrodeposition method and characterized by X-ray diffraction (XRD) and scanning electron microscopy (SEM). The electrochemical performance of the prepared electrode is evaluated through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Results show that PbO2 exhibits excellent electro-catalytic activity and reactive velocity to vanadium redox couples. The coulombic efficiency (CE), voltage efficiency (VE), and energy efficiency (EE) of the vanadium redox flow battery with as-prepared electrodes at 70 mA cm-2 are 99.5%, 82.4%, and 82.0%, respectively; these values are much higher than those of a cell assembled with bare graphite felt electrodes. The outstanding electro-catalytic activity and mechanical stability of PbO2 are advantageous in facilitating the redox reaction of vanadium ions, leading to the efficient operation of a vanadium redox flow battery.

  14. Quantitative probe of the transition metal redox in battery electrodes through soft x-ray absorption spectroscopy

    Science.gov (United States)

    Li, Qinghao; Qiao, Ruimin; Wray, L. Andrew; Chen, Jun; Zhuo, Zengqing; Chen, Yanxue; Yan, Shishen; Pan, Feng; Hussain, Zahid; Yang, Wanli

    2016-10-01

    Most battery positive electrodes operate with a 3d transition-metal (TM) reaction centre. A direct and quantitative probe of the TM states upon electrochemical cycling is valuable for understanding the detailed cycling mechanism and charge diffusion in the electrodes, which is related with many practical parameters of a battery. This review includes a comprehensive summary of our recent demonstrations of five different types of quantitative analysis of the TM states in battery electrodes based on soft x-ray absorption spectroscopy and multiplet calculations. In LiFePO4, a system of a well-known two-phase transformation type, the TM redox could be strictly determined through a simple linear combination of the two end-members. In Mn-based compounds, the Mn states could also be quantitatively evaluated, but a set of reference spectra with all the three possible Mn valences needs to be deliberately selected and considered in the fitting. Although the fluorescence signals suffer the self-absorption distortion, the multiplet calculations could consider the distortion effect, which allows a quantitative determination of the overall Ni oxidation state in the bulk. With the aid of multiplet calculations, one could also achieve a quasi-quantitative analysis of the Co redox evolution in LiCoO2 based on the energy position of the spectroscopic peak. The benefit of multiplet calculations is more important for studying electrode materials with TMs of mixed spin states, as exemplified by the quantitative analysis of the mixed spin Na2-x Fe2(CN)6 system. At the end, we showcase that such quantitative analysis could provide valuable information for optimizing the electrochemical performance of Na0.44MnO2 electrodes for Na-ion batteries. The methodology summarized in this review could be extended to other energy application systems with TM redox centre for detailed analysis, for example, fuel cell and catalytic materials.

  15. Method of fabricating electrodes including high-capacity, binder-free anodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Ban, Chunmei; Wu, Zhuangchun; Dillon, Anne C.

    2017-01-10

    An electrode (110) is provided that may be used in an electrochemical device (100) such as an energy storage/discharge device, e.g., a lithium-ion battery, or an electrochromic device, e.g., a smart window. Hydrothermal techniques and vacuum filtration methods were applied to fabricate the electrode (110). The electrode (110) includes an active portion (140) that is made up of electrochemically active nanoparticles, with one embodiment utilizing 3d-transition metal oxides to provide the electrochemical capacity of the electrode (110). The active material (140) may include other electrochemical materials, such as silicon, tin, lithium manganese oxide, and lithium iron phosphate. The electrode (110) also includes a matrix or net (170) of electrically conductive nanomaterial that acts to connect and/or bind the active nanoparticles (140) such that no binder material is required in the electrode (110), which allows more active materials (140) to be included to improve energy density and other desirable characteristics of the electrode. The matrix material (170) may take the form of carbon nanotubes, such as single-wall, double-wall, and/or multi-wall nanotubes, and be provided as about 2 to 30 percent weight of the electrode (110) with the rest being the active material (140).

  16. Relating the 3D electrode morphology to Li-ion battery performance; a case for LiFePO4

    Science.gov (United States)

    Liu, Zhao; Verhallen, Tomas W.; Singh, Deepak P.; Wang, Hongqian; Wagemaker, Marnix; Barnett, Scott

    2016-08-01

    One of the main goals in lithium ion battery electrode design is to increase the power density. This requires insight in the relation between the complex heterogeneous microstructure existing of active material, conductive additive and electrolyte providing the required electronic and Li-ion transport. FIB-SEM is used to determine the three phase 3D morphology, and Li-ion concentration profiles obtained with Neutron Depth Profiling (NDP) are compared for two cases, conventional LiFePO4 electrodes and better performing carbonate templated LiFePO4 electrodes. This provides detailed understanding of the impact of key parameters such as the tortuosity for electron and Li-ion transport though the electrodes. The created hierarchical pore network of the templated electrodes, containing micron sized pores, appears to be effective only at high rate charge where electrolyte depletion is hindering fast discharge. Surprisingly the carbonate templating method results in a better electronic conductive CB network, enhancing the activity of LiFePO4 near the electrolyte-electrode interface as directly observed with NDP, which in a large part is responsible for the improved rate performance both during charge and discharge. The results demonstrate that standard electrodes have a far from optimal charge transport network and that significantly improved electrode performance should be possible by engineering the microstructure.

  17. Laser-perforated carbon paper electrodes for improved mass-transport in high power density vanadium redox flow batteries

    Science.gov (United States)

    Mayrhuber, I.; Dennison, C. R.; Kalra, V.; Kumbur, E. C.

    2014-08-01

    In this study, we demonstrate up to 30% increase in power density of carbon paper electrodes for vanadium redox flow batteries (VRFB) by introducing perforations into the structure of electrodes. A CO2 laser was used to generate holes ranging from 171 to 421 μm diameter, and hole densities from 96.8 to 649.8 holes cm-2. Perforation of the carbon paper electrodes was observed to improve cell performance in the activation region due to thermal treatment of the area around the perforations. Results also demonstrate improved mass transport, resulting in enhanced peak power and limiting current density. However, excessive perforation of the electrode yielded a decrease in performance due to reduced available surface area. A 30% increase in peak power density (478 mW cm-2) was observed for the laser perforated electrode with 234 μm diameter holes and 352.8 holes cm-2 (1764 holes per 5 cm2 electrode), despite a 15% decrease in total surface area compared to the raw un-perforated electrode. Additionally, the effect of perforation on VRFB performance was studied at different flow rates (up to 120 mL min-1) for the optimized electrode architecture. A maximum power density of 543 mW cm-2 was achieved at 120 mL min-1.

  18. A new strategy for integrating abundant oxygen functional groups into carbon felt electrode for vanadium redox flow batteries

    Science.gov (United States)

    Kim, Ki Jae; Lee, Seung-Wook; Yim, Taeeun; Kim, Jae-Geun; Choi, Jang Wook; Kim, Jung Ho; Park, Min-Sik; Kim, Young-Jun

    2014-11-01

    The effects of surface treatment combining corona discharge and hydrogen peroxide (H2O2) on the electrochemical performance of carbon felt electrodes for vanadium redox flow batteries (VRFBs) have been thoroughly investigated. A high concentration of oxygen functional groups has been successfully introduced onto the surface of the carbon felt electrodes by a specially designed surface treatment, which is mainly responsible for improving the energy efficiency of VRFBs. In addition, the wettability of the carbon felt electrodes also can be significantly improved. The energy efficiency of the VRFB cell employing the surface modified carbon felt electrodes is improved by 7% at high current density (148 mA cm-2). Such improvement is attributed to the faster charge transfer and better wettability allowed by surface-active oxygen functional groups. Moreover, this method is much more competitive than other surface treatments in terms of processing time, production costs, and electrochemical performance.

  19. Effects of additional multiwall carbon nanotubes on impact behaviors of LiNi0.5Mn0.3Co0.2O2 battery electrodes

    Science.gov (United States)

    Le, Anh V.; Wang, Meng; Shi, Yang; Noelle, Daniel; Qiao, Yu; Lu, Weiyi

    2015-08-01

    This work introduces a new mechanically triggered thermal runaway mitigation mechanism. The homogenizer of electrode failure (HEF), multiwall carbon nanotube (MWCNT), was added into LiNi0.5Mn0.3Co0.2O2 (NMC532) battery electrodes. We have studied the effect of the HEF additive on the internal electrical resistance and the mechanical impact resistance of the electrodes. The additional MWCNTs reduced the internal electrical resistance of electrodes before mechanical abuse. Upon mechanical abuse, they could mitigate internal shorting and thermal runaway at normal battery working temperature.

  20. Origins of Large Voltage Hysteresis in High-Energy-Density Metal Fluoride Lithium-Ion Battery Conversion Electrodes.

    Science.gov (United States)

    Li, Linsen; Jacobs, Ryan; Gao, Peng; Gan, Liyang; Wang, Feng; Morgan, Dane; Jin, Song

    2016-03-02

    Metal fluorides and oxides can store multiple lithium ions through conversion chemistry to enable high-energy-density lithium-ion batteries. However, their practical applications have been hindered by an unusually large voltage hysteresis between charge and discharge voltage profiles and the consequent low-energy efficiency (hysteresis are rarely studied and poorly understood. Here we employ in situ X-ray absorption spectroscopy, transmission electron microscopy, density functional theory calculations, and galvanostatic intermittent titration technique to first correlate the voltage profile of iron fluoride (FeF3), a representative conversion electrode material, with evolution and spatial distribution of intermediate phases in the electrode. The results reveal that, contrary to conventional belief, the phase evolution in the electrode is symmetrical during discharge and charge. However, the spatial evolution of the electrochemically active phases, which is controlled by reaction kinetics, is different. We further propose that the voltage hysteresis in the FeF3 electrode is kinetic in nature. It is the result of ohmic voltage drop, reaction overpotential, and different spatial distributions of electrochemically active phases (i.e., compositional inhomogeneity). Therefore, the large hysteresis can be expected to be mitigated by rational design and optimization of material microstructure and electrode architecture to improve the energy efficiency of lithium-ion batteries based on conversion chemistry.

  1. Effect of local velocity on diffusion-induced stress in large-deformation electrodes of lithium-ion batteries

    Science.gov (United States)

    Li, Yong; Zhang, Kai; Zheng, Bailin; Yang, Fuqian

    2016-07-01

    In this work, the contribution of local velocity to the resultant flux of lithium in lithium-ion battery is introduced into the diffusion equation to describe the migration of lithium in the active material of electrodes. The effect of the local velocity on the stress evolution in a spherical electrode made of silicon is analyzed, using the derived diffusion equation and nonlinear theory of elasticity. Two boundary conditions at the surface of the electrode, which represent two extreme conditions of real electrode materials, are used in the stress analysis: one is stress-free, and the other is immobile. The numerical results with the stress-free boundary condition suggest that the effect of the local velocity on the distribution of radial stress and hoop stress increases with the increase of time and the effect of the local velocity on the distribution of lithium is relatively small. In comparison with the results without the effect of the local velocity, the effect of the local velocity is negligible for the immobile boundary condition. The numerical result shows that the use of the immobile boundary condition leads to the decrease of von-Mises stress, which likely will retard the mechanical degradation of electrode and improve the electrochemical performance of lithium-ion battery.

  2. Carbon felt and carbon fiber - A techno-economic assessment of felt electrodes for redox flow battery applications

    Science.gov (United States)

    Minke, Christine; Kunz, Ulrich; Turek, Thomas

    2017-02-01

    Carbon felt electrodes belong to the key components of redox flow batteries. The purpose of this techno-economic assessment is to uncover the production costs of PAN- and rayon-based carbon felt electrodes. Raw material costs, energy demand and the impact of processability of fiber and felt are considered. This innovative, interdisciplinary approach combines deep insights into technical, ecologic and economic aspects of carbon felt and carbon fiber production. Main results of the calculation model are mass balances, cumulative energy demands (CED) and the production costs of conventional and biogenic carbon felts supplemented by market assessments considering textile and carbon fibers.

  3. Manufacturing of Protected Lithium Electrodes for Advanced Lithium-Air, Lithium-Water & Lithium-Sulfur Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Visco, Steven J

    2015-11-30

    The global demand for rechargeable batteries is large and growing rapidly. Assuming the adoption of electric vehicles continues to increase, the need for smaller, lighter, and less expensive batteries will become even more pressing. In this vein, PolyPlus Battery Company has developed ultra-light high performance batteries based on its proprietary protected lithium electrode (PLE) technology. The Company’s Lithium-Air and Lithium-Seawater batteries have already demonstrated world record performance (verified by third party testing), and we are developing advanced lithium-sulfur batteries which have the potential deliver high performance at low cost. In this program PolyPlus Battery Company teamed with Corning Incorporated to transition the PLE technology from bench top fabrication using manual tooling to a pre- commercial semi-automated pilot line. At the inception of this program PolyPlus worked with a Tier 1 battery manufacturing engineering firm to design and build the first-of-its-kind pilot line for PLE production. The pilot line was shipped and installed in Berkeley, California several months after the start of the program. PolyPlus spent the next two years working with and optimizing the pilot line and now produces all of its PLEs on this line. The optimization process successfully increased the yield, throughput, and quality of PLEs produced on the pilot line. The Corning team focused on fabrication and scale-up of the ceramic membranes that are key to the PLE technology. PolyPlus next demonstrated that it could take Corning membranes through the pilot line process to produce state-of-the-art protected lithium electrodes. In the latter part of the program the Corning team developed alternative membranes targeted for the large rechargeable battery market. PolyPlus is now in discussions with several potential customers for its advanced PLE-enabled batteries, and is building relationships and infrastructure for the transition into manufacturing. It is likely

  4. Ultra-fast dry microwave preparation of SnSb used as negative electrode material for Li-ion batteries

    Science.gov (United States)

    Antitomaso, P.; Fraisse, B.; Sougrati, M. T.; Morato-Lallemand, F.; Biscaglia, S.; Aymé-Perrot, D.; Girard, P.; Monconduit, L.

    2016-09-01

    Tin antimonide alloy was obtained for the first time using a very simple dry microwave route. Up to 1 g of well crystallized SnSb can be easily prepared in 90 s under air in an open crucible. A full characterization by X-ray diffraction and 119Sn Mössbauer spectroscopy demonstrated the benefit of carbon as susceptor, which avoid any oxide contamination. The microwave-prepared SnSb was tested as negative electrode material in Li batteries. Interesting results in terms of capacity and rate capability were obtained with up to 700 mAh/g sustained after 50 cycles at variable current. These results pave the way for the introduction of microwave synthesis as realistic route for a rapid, low cost and up-scalable production of electrode material for Li batteries or other large scale application types.

  5. Nitrogen-Doped Carbon Nanotube/Graphite Felts as Advanced Electrode Materials for Vanadium Redox Flow Batteries.

    Science.gov (United States)

    Wang, Shuangyin; Zhao, Xinsheng; Cochell, Thomas; Manthiram, Arumugam

    2012-08-16

    Nitrogen-doped carbon nanotubes have been grown, for the first time, on graphite felt (N-CNT/GF) by a chemical vapor deposition approach and examined as an advanced electrode for vanadium redox flow batteries (VRFBs). The unique porous structure and nitrogen doping of N-CNT/GF with increased surface area enhances the battery performance significantly. The enriched porous structure of N-CNTs on graphite felt could potentially facilitate the diffusion of electrolyte, while the N-doping could significantly contribute to the enhanced electrode performance. Specifically, the N-doping (i) modifies the electronic properties of CNT and thereby alters the chemisorption characteristics of the vanadium ions, (ii) generates defect sites that are electrochemically more active, (iii) increases the oxygen species on CNT surface, which is a key factor influencing the VRFB performance, and (iv) makes the N-CNT electrochemically more accessible than the CNT.

  6. 锂离子电池电极材料选择%Electrode Materials for Lithium Ion Battery

    Institute of Scientific and Technical Information of China (English)

    张临超; 陈春华

    2011-01-01

    It has been 20 years since lithium ion battery appeared as a commercial product. Different kinds of new electrode materials are urgently needed to meet the demands of the society. In this review, some knowledge about lithium ion battery is first given. Then we focus on several new positive/negative electrode materials reported up to date. When they were used as lithium ion battery electrode materials, how they are synthesized, the main improvement methods and their electrochemical performance will be presented. Finally, we give a short summary of the advantages/disadvantages of these new electrode materials. Furthermore, an outlook for the potential applications of lithium ion batteries in the future is proposed.%商用锂离子电池发展至今已有20年,为了满足不同方面的社会需求,人们迫切需要新型锂离子电池电极材料.本文首先简要介绍了锂离子电池的相关知识,随后对多种新型锂离子电池正负极材料的制备、改进方法及电化学性能做了详细介绍,最后对各种电极材料的优缺点进行了简要的总结.本文还对锂离子电池在未来的应用进行了展望,以期待锂离子电池更好地为人类服务.

  7. Development of Novel Metal Hydride-Carbon Nanomaterial Based Nanocomposites as Anode Electrode Materials for Lithium Ion Battery

    Science.gov (United States)

    2014-06-30

    Final Progress Report (27-02-2012 To 26-02-2014) Project Title:- Development of novel metal hydride -carbon nanomaterial based nanocomposites as...anode electrode materials for Lithium ion battery Objectives:- The aim of this study is to develop metal hydride –carbon nanomaterial based...be as follows:- Milestone I • Synthesis of nanosized metal hydrides (NMH)-carbon nanotubes (CNT) hybridizing with G (NMH- CNT-G) nanocomposites

  8. Mass spectrometry investigations on electrolyte degradation products for the development of nanocomposite electrodes in lithium ion batteries.

    Science.gov (United States)

    Gireaud, Laurent; Grugeon, Sylvie; Pilard, Serge; Guenot, Pierre; Tarascon, Jean-Marie; Laruelle, Stephane

    2006-06-01

    In the continuing challenge to find new routes to improve the performance of commercial lithium ion batteries cycling in alkyl carbonate-based electrolyte solutions, original designs, and new electrode materials are under active worldwide investigation. Our group has focused on the electrochemical behavior of a new generation of nanocomposite electrodes showing improved capacities (up to 3 times the capacity of conventional electrode materials). However, moving down to "nanometric-scale" active materials leads to a significant increase in electrolyte degradation, compared to that taking place within commercial batteries. Postmortem electrolyte studies on experimental coin cells were conducted to understand the degradation mechanisms. Structural analysis of the organic degradation products were investigated using a combination of complementary high-resolution mass spectrometry techniques: desorption under electron impact, electrospray ionization, and gas chromatography coupled to a mass spectrometer equipped with electron impact and chemical ionization ion sources. Numerous organic degradation products such as ethylene oxide oligomers (with methyl, hydroxyl, phosphate, and methyl carbonate endings) have been characterized. In light of our findings, possible chemical or electrochemical pathways are proposed to account for their formation. A thorough knowledge of these degradation mechanisms will enable us to propose new electrolyte formulations to optimize nanocomposite-based lithium ion battery performance.

  9. Bicontinuous gyroid nickel network derived from a block copolymer template for three-dimensional MnO₂ electrodes as nanostructured, dimensionally-stabilized lithium-ion battery anodes

    NARCIS (Netherlands)

    Tillmann, Selina; Cekic-Laskovic, Isadora; Winter, Martin; Loos, Katja

    2016-01-01

    To improve lithium-ion batteries further, novel concepts for the reproducible preparation of highly structured bicontinuous battery electrodes are required. With this in mind, the main focus of this work is set on the block copolymer template-directed synthesis of metal nanofoams suitable for the ra

  10. High-performance graphene/sulphur electrodes for flexible Li-ion batteries using the low-temperature spraying method

    KAUST Repository

    Kumar, Pushpendra

    2015-01-01

    Elementary sulphur (S) has been shown to be an excellent cathode material in energy storage devices such as Li-S batteries owing to its very high capacity. The major challenges associated with the sulphur cathodes are structural degradation, poor cycling performance and instability of the solid-electrolyte interphase caused by the dissolution of polysulfides during cycling. Tremendous efforts made by others have demonstrated that encapsulation of S materials improves their cycling performance. To make this approach practical for large scale applications, the use of low-cost technology and materials has become a crucial and new focus of S-based Li-ion batteries. Herein, we propose to use a low temperature spraying process to fabricate graphene/S electrode material, where the ink is composed of graphene flakes and the micron-sized S particles prepared by grinding of low-cost S powders. The S particles are found to be well hosted by highly conductive graphene flakes and consequently superior cyclability (∼70% capacity retention after 250 cycles), good coulombic efficiency (∼98%) and high capacity (∼1500 mA h g-1) are obtained. The proposed approach does not require high temperature annealing or baking; hence, another great advantage is to make flexible Li-ion batteries. We have also demonstrated two types of flexible batteries using sprayed graphene/S electrodes. © The Royal Society of Chemistry 2015.

  11. Olivine-Based Blended Compounds as Positive Electrodes for Lithium Batteries

    Directory of Open Access Journals (Sweden)

    Christian M. Julien

    2016-05-01

    Full Text Available Blended cathode materials made by mixing LiFePO4 (LFP with LiMnPO4 (LMP or LiNi1/3Mn1/3Co1/3O2 (NMC that exhibit either high specific energy and high rate capability were investigated. The layered blend LMP–LFP and the physically mixed blend NMC–LFP are evaluated in terms of particle morphology and electrochemical performance. Results indicate that the LMP–LFP (66:33 blend has a better discharge rate than the LiMn1−yFeyPO4 with the same composition (y = 0.33, and NMC–LFP (70:30 delivers a remarkable stable capacity over 125 cycles. Finally, in situ voltage measurement methods were applied for the evaluation of the phase evolution of blended cathodes and gradual changes in cell behavior upon cycling. We also discuss through these examples the promising development of blends as future electrodes for new generations of Li-ion batteries.

  12. Pulsed laser deposited FeOF as negative electrodes for rechargeable Li batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yu Le; Wang Haoxuan; Liu Zhiyan [Shanghai Key laboratory of Molecular Catalysts and Innovative Materials, Department of Chemistry and Laser Chemistry Institute, Fudan University, Shanghai, 200433 (China); Fu Zhengwen, E-mail: zwfu@fudan.edu.c [Shanghai Key laboratory of Molecular Catalysts and Innovative Materials, Department of Chemistry and Laser Chemistry Institute, Fudan University, Shanghai, 200433 (China)

    2010-12-30

    FeOF thin film has been successfully fabricated by reactive pulsed laser deposition for the first time, and its electrochemical behavior was examined as a negative electrode active material in lithium-ion batteries. The electrochemical properties of the as-deposited FeOF thin film during the first charging and discharging have been investigated by the galvanostatic cycling and cyclic voltammetry measurements. By using ex situ X-ray diffraction (XRD), X-ray photoelectron spectra (XPS), scanning electron microscopy (SEM), transmission electron microscopy (TEM), and selected-area electron diffraction measurements (SAED), it can be found that FeOF was initially decomposed into Fe{sup 0}, LiF, and Fe{sub 2}O{sub 3} after discharging to 1.0 V. The newly formed Fe{sub 2}O{sub 3} is then subsequently reduced into Li{sub 2}O and Fe{sup 0} after further discharging to 0.01 V. In the subsequent cycle, the reduction peaks at 0.76 V and the oxidation-reduction peaks at 1.6 and 1.9 V could be attributed to the reversible decomposition and formation of Li{sub 2}O with the conversion reaction of Fe{sub 2}O{sub 3} into Fe.

  13. CuSbS2 as a negative electrode material for sodium ion batteries

    Science.gov (United States)

    Marino, C.; Block, T.; Pöttgen, R.; Villevieille, C.

    2017-02-01

    CuSbS2 was tested as a negative electrode material for sodium-ion batteries. The material synthesized by ball milling offers a specific charge of 730 mAh g-1, close to the theoretical value (751 mAh g-1), over a few cycles. The reaction mechanism was investigated by means of operando X-ray diffraction, 121Sb Mössbauer spectroscopy, and Cu K-edge X-ray absorption spectroscopy. These studies reveal a sodiation mechanism that involves an original conversion reaction in two steps, through the formation of a ternary phase, CuSb(1-x)S(2-y), as well as a NaxS alloy and Sb, followed by an alloying reaction involving the previously formed Sb. The desodiation process ends with the reformation of the ternary phase, CuSb(1-x‧)S(2-y‧), deficient in Sb and S; this phase is responsible for the good reversibility observed upon cycling.

  14. Effects of surface tension and electrochemical reactions in Li-ion battery electrode nanoparticles

    Science.gov (United States)

    Stein, Peter; Zhao, Ying; Xu, Bai-Xiang

    2016-11-01

    The size- and shape-dependency of the chemo-mechanical behavior of spherical and ellipsoidal nanoparticles in Li-ion battery electrodes are investigated by a stress-assisted diffusion model and 3D finite element simulations. The model features surface tension, a direct coupling between diffusion and elasticity, concentration-dependent diffusivity, and a Butler-Volmer relation for the description of electrochemical reactions that is modified to account for mechanical effects. Simulation results on spherical particles reveal that surface tension causes additional pressure fields in the particles, shifting the stress state towards the compressive regime. This provides mechanical stabilization, allowing, in principle, for higher charge/discharge rates. However, due to this pressure the attainable lithiation for a given potential difference is reduced during insertion, whereas a higher amount of ions is given off during extraction. Ellipsoidal particles with an aspect ratio deviating from that of a sphere with the same volume expose a larger surface area to the intercalation reactions. Consequently, they exhibit accelerated (dis)charge rates. However, due to the enhanced pressure in regions with high curvature, the accessible capacity of ellipsoidal particles is less than that of spherical particles.

  15. Performance and cycle life of carbon- and conductive-based air electrodes for rechargeable Zn-air battery applications

    Science.gov (United States)

    Chellapandi Velraj, Samgopiraj

    The development of high-performance, cyclically stable bifunctional air electrodes are critical to the commercial deployment of rechargeable Zn-air batteries. The carbon material predominantly used as support material in the air electrodes due to its higher surface area and good electrical conductivity suffers from corrosion at high oxygen evolution overpotentials. This study addresses the carbon corrosion issues and suggests alternate materials to replace the carbon as support in the air electrode. In this study, Sm0.5Sr0.5CoO3-delta with good electrochemical performance and cyclic lifetime was identified as an alternative catalyst material to the commonly used La0.4Ca 0.6CoO3 catalyst for the carbon-based bifunctional electrodes. Also, a comprehensive study on the effects of catalyst morphology, testing conditions on the cycle life as well as the relevant degradation mechanism for the carbon-based electrode was conducted in this dissertation. The cyclic life of the carbon-based electrodes was strongly dependent on the carbon support material, while the degradation mechanisms were entirely controlled by the catalyst particle size/morphology. Some testing conditions like resting time and electrolyte concentration did not change the cyclic life or degradation mechanism of the carbon-based electrode. The current density used for cyclic testing was found to dictate the degradation mechanism leading to the electrode failure. An alternate way to circumvent the carbon corrosion is to replace the carbon support with a suitable electrically-conductive ceramic material. In this dissertation, LaNi0.9Mn0.1O3, LaNi 0.8Co0.2O3, and NiCo2O4 were synthesized and evaluated as prospective support materials due to their good electrical conductivity and their ability to act as the catalyst needed for the bifunctional electrode. The carbon-free electrodes had remarkably higher catalytic activity for oxygen evolution reaction (OER) when compared to the carbon-based electrode. However

  16. Polyaniline silver nanoparticle coffee waste extracted porous graphene oxide nanocomposite structures as novel electrode material for rechargeable batteries

    Science.gov (United States)

    Sundriyal, Poonam; Bhattacharya, Shantanu

    2017-03-01

    The exploration of new and advanced electrode materials are required in electronic and electrical devices for power storage applications. Also, there has been a continuous endeavour to formulate strategies for extraction of high performance electrode materials from naturally obtained waste products. In this work, we have developed an in situ hybrid nanocomposite from coffee waste extracted porous graphene oxide (CEPG), polyaniline (PANI) and silver nanoparticles (Ag) and have found this novel composite to serve as an efficient electrode material for batteries. The successful interaction among the three phases of the nano-composite i.e. CEPG–PANI–Ag have been thoroughly understood through RAMAN, Fourier transform infrared and x-ray diffraction spectroscopy, morphological studies through field emission scanning electron microscope and transmission electron microscope. Thermo-gravimetric analysis of the nano-composite demonstrates higher thermal stability up-to a temperature of 495 °C. Further BET studies through nitrogen adsorption–desorption isotherms confirm the presence of micro/meso and macro-pores in the nanocomposite sample. The cyclic-voltammetry (CV) analysis performed on CEPG–PANI–Ag nanocomposite exhibits a purely faradic behaviour using nickel foam as a current collector thus suggests the prepared nanocomposite as a battery electrode material. The nanocomposite reports a maximum specific capacity of 1428 C g‑1 and excellent cyclic stability up-to 5000 cycles.

  17. Importance of open pore structures with mechanical integrity in designing the cathode electrode for lithium-sulfur batteries

    Science.gov (United States)

    Kim, C.-S.; Guerfi, A.; Hovington, P.; Trottier, J.; Gagnon, C.; Barray, F.; Vijh, A.; Armand, M.; Zaghib, K.

    2013-11-01

    The robustness of conductive networks and the accessibility of electrolyte into the network are important factors in designing the cathode electrode for lithium/sulfur (Li/S) batteries containing liquid electrolytes that involve liquid phase electrochemical reactions. We show that the performance of Li/S cells can be significantly improved by simply optimizing the electrode processing conditions to have open pore structures and mechanical integrity of the electrode architecture. It is demonstrated that the capacity of 1000 mAh g-1 at 0.1 C and the stable capacity retention of >700 mAh g-1 after 200 cycles at 0.5 C can be achieved with relatively high sulfur content of 68%. 417 Wh kg-1 in specific energy and 623 Wh l-1 in energy density are achievable with this new technology.

  18. Asymmetric pathways in the electrochemical conversion reaction of NiO as battery electrode with high storage capacity

    Science.gov (United States)

    Boesenberg, Ulrike; Marcus, Matthew A.; Shukla, Alpesh K.; Yi, Tanghong; McDermott, Eamon; Teh, Pei Fen; Srinivasan, Madhavi; Moewes, Alexander; Cabana, Jordi

    2014-11-01

    Electrochemical conversion reactions of transition metal compounds create opportunities for large energy storage capabilities exceeding modern Li-ion batteries. However, for practical electrodes to be envisaged, a detailed understanding of their mechanisms is needed, especially vis-à-vis the voltage hysteresis observed between reduction and oxidation. Here, we present such insight at scales from local atomic arrangements to whole electrodes. NiO was chosen as a simple model system. The most important finding is that the voltage hysteresis has its origin in the differing chemical pathways during reduction and oxidation. This asymmetry is enabled by the presence of small metallic clusters and, thus, is likely to apply to other transition metal oxide systems. The presence of nanoparticles also influences the electrochemical activity of the electrolyte and its degradation products and can create differences in transport properties within an electrode, resulting in localized reactions around converted domains that lead to compositional inhomogeneities at the microscale.

  19. Bismuth nanoparticle decorating graphite felt as a high-performance electrode for an all-vanadium redox flow battery.

    Science.gov (United States)

    Li, Bin; Gu, Meng; Nie, Zimin; Shao, Yuyan; Luo, Qingtao; Wei, Xiaoliang; Li, Xiaolin; Xiao, Jie; Wang, Chongmin; Sprenkle, Vincent; Wang, Wei

    2013-03-13

    Employing electrolytes containing Bi(3+), bismuth nanoparticles are synchronously electrodeposited onto the surface of a graphite felt electrode during operation of an all-vanadium redox flow battery (VRFB). The influence of the Bi nanoparticles on the electrochemical performance of the VRFB is thoroughly investigated. It is confirmed that Bi is only present at the negative electrode and facilitates the redox reaction between V(II) and V(III). However, the Bi nanoparticles significantly improve the electrochemical performance of VRFB cells by enhancing the kinetics of the sluggish V(II)/V(III) redox reaction, especially under high power operation. The energy efficiency is increased by 11% at high current density (150 mA·cm(-2)) owing to faster charge transfer as compared with one without Bi. The results suggest that using Bi nanoparticles in place of noble metals offers great promise as high-performance electrodes for VRFB application.

  20. Strong dependency of lithium diffusion on mechanical constraints in high-capacity Li-ion battery electrodes

    Institute of Scientific and Technical Information of China (English)

    Yi-Fan Gao; Min Zhou

    2012-01-01

    The effect of external constraints on Li diffusion in high-capacity Li-ion battery electrodes is investigated using a coupled finite deformation theory.It is found that thinfilm electrodes on rigid substrates experience much slower diffusion rates compared with free-standing films with the same material properties and geometric dimensions.More importantly,the study reveals that mechanical driving forces tend to retard diffusion in highly-constrained thin films when lithiation-induced softening is considered,in contrast to the fact that mechanical driving forces always enhance diffusion when deformation is fully elastic.The results provide further proof that nano-particles are a better design option for nextgeneration alloy-based electrodes compared with thin films.

  1. Asymmetric pathways in the electrochemical conversion reaction of NiO as battery electrode with high storage capacity.

    Science.gov (United States)

    Boesenberg, Ulrike; Marcus, Matthew A; Shukla, Alpesh K; Yi, Tanghong; McDermott, Eamon; Teh, Pei Fen; Srinivasan, Madhavi; Moewes, Alexander; Cabana, Jordi

    2014-11-20

    Electrochemical conversion reactions of transition metal compounds create opportunities for large energy storage capabilities exceeding modern Li-ion batteries. However, for practical electrodes to be envisaged, a detailed understanding of their mechanisms is needed, especially vis-à-vis the voltage hysteresis observed between reduction and oxidation. Here, we present such insight at scales from local atomic arrangements to whole electrodes. NiO was chosen as a simple model system. The most important finding is that the voltage hysteresis has its origin in the differing chemical pathways during reduction and oxidation. This asymmetry is enabled by the presence of small metallic clusters and, thus, is likely to apply to other transition metal oxide systems. The presence of nanoparticles also influences the electrochemical activity of the electrolyte and its degradation products and can create differences in transport properties within an electrode, resulting in localized reactions around converted domains that lead to compositional inhomogeneities at the microscale.

  2. Influence of inactive electrode components on degradation phenomena in nano-Si electrodes for Li-ion batteries

    Science.gov (United States)

    Jeschull, Fabian; Lindgren, Fredrik; Lacey, Matthew J.; Björefors, Fredrik; Edström, Kristina; Brandell, Daniel

    2016-09-01

    The electrode morphology and electrochemistry of silicon nanocomposite electrodes containing either carboxymethyl cellulose (CMC-Na) or poly(acrylic acid) (PAA) binders are examined in context of their working surface area. Using porous carbon (Ketjenblack) additives, coatings with poor adhesion properties and deep cracks were obtained. The morphology is also reflected in the electrochemical behavior under capacity-limited conditions. Mapping the differential capacity versus potential over all cycles yields detailed insights into the degradation processes and shows the onset of cell failure with the emergence of lithium-rich silicon alloys at low potentials, well before capacity fading is observed. Fading occurs faster with electrodes containing PAA binder. The surface area of the electrode components is a major cause of increased irreversible reaction and capacity fade. Synchrotron-based X-ray photoelectron spectroscopy on aged, uncycled electrodes revealed accelerated conversion of the native SiOx-layer to detrimental SiOxFy in presence of Ketjenblack. In contrast, a conventional carbon black better preserved the SiOx-layer. This effect is attributed to preferred adsorption of binder on high surface area electrode components and highlights the role of binders as 'artificial SEI-layers'. This work demonstrates that optimization of nanocomposites requires careful balancing of the surface areas and amounts of all the electrode components applied.

  3. Composite metal-hydrogen electrodes for metal-hydrogen batteries. Final report, October 1, 1993--April 15, 1997

    Energy Technology Data Exchange (ETDEWEB)

    Ruckman, M.W.; Strongin, M.; Weismann, H. [and others

    1997-04-01

    The purpose of this project is to develop and conduct a feasibility study of metallic thin films (multilayered and alloy composition) produced by advanced sputtering techniques for use as anodes in Ni-metal hydrogen batteries that would be deposited as distinct anode, electrolyte and cathode layers in thin film devices. The materials could also be incorporated in secondary consumer batteries (i.e. type AF(4/3 or 4/5)) which use electrodes in the form of tapes. The project was based on pioneering studies of hydrogen uptake by ultra-thin Pd-capped Nb films, these studies suggested that materials with metal-hydrogen ratios exceeding those of commercially available metal hydride materials and fast hydrogen charging and discharging kinetics could be produced. The project initially concentrated on gas phase and electrochemical studies of Pd-capped niobium films in laboratory-scale NiMH cells. This extended the pioneering work to the wet electrochemical environment of NiMH batteries and exploited advanced synchrotron radiation techniques not available during the earlier work to conduct in-situ studies of such materials during hydrogen charging and discharging. Although batteries with fast charging kinetics and hydrogen-metal ratios approaching unity could be fabricated, it was found that oxidation, cracking and corrosion in aqueous solutions made pure Nb films and multilayers poor candidates for battery application. The project emphasis shifted to alloy films based on known elemental materials used for NiMH batteries. Although commercial NiMH anode materials contain many metals, it was found that 0.24 {mu}m thick sputtered Zr-Ni films cycled at least 50 times with charging efficiencies exceeding 95% and [H]/[M] ratios of 0.7-1.0. Multilayered or thicker Zr-Ni films could be candidates for a thin film NiMH battery that may have practical applications as an integrated power source for modern electronic devices.

  4. Solid state NMR and pair distribution function studies of silicon electrodes for lithium-ion batteries

    Science.gov (United States)

    Key, Baris

    The universally used negative electrode material in a LIB is carbon, because of its moderate capacity (372 mAhg-1 for graphite), cyclability and high rate capability. However, new, low cost, safe electrode materials with higher capacities are still urgently required for both portable and transportation applications. Silicon anodes are particularly attractive alternatives to carbon with extremely high gravimetric energy densities (3572 mAhg-1). Compared to graphite, silicon has a massive volumetric capacity of 8322 mAhcm-3 (calculated based on the original volume of silicon) which is approximately ten times that graphite. At room temperature, upon electrochemical lithiation, silicon undergoes a crystalline to amorphous phase transition forming a lithiated amorphous silicide phase. Unfortunately, due to the amorphous nature of the lithiated silicides, it is not possible to monitor all the structural changes that occur during lithium insertion/removal with conventional methods such as diffraction. The short range order of the amorphous materials remains unknown, preventing attempts to optimize performance based on electrochemical-structure correlations. In this work, a combination of local structure probes, ex-situ 7Li nuclear magnetic resonance (NMR) studies and pair distribution function (PDF) analysis of X-ray data was applied to investigate the changes in short range order that occur during the initial charge and discharge cycles. The distinct electrochemical profiles observed subsequent to the 1 st discharge have been shown to be associated with the formation of distinct amorphous lithiated silicide structures. A (de)lithiation model consisting of four different mechanisms, each being valid for regions of the charge or discharge process is proposed to explain the hysteresis and the steps in the electrochemical profile observed during lithiation and delithiation of Si. A spontaneous reaction of the fully lithiated lithium silicide with the electrolyte is directly

  5. Conversion Reaction Mechanisms in Lithium Ion Batteries: Study of the Binary Metal Fluoride Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Feng; Robert, Rosa; Chernova, Natasha A.; Pereira, Nathalie; Omenya, Fredrick; Badway, Fadwa; Hua, Xiao; Ruotolo, Michael; Zhang, Ruigang; Wu, Lijun; Volkov, Vyacheslav; Su, Dong; Key, Baris; Whittingham, M. Stanley; Grey, Clare P.; Amatucci, Glenn G.; Zhu, Yimei; Graetz, Jason (Binghamton); (Rutgers); (BNL); (Cambridge); (SBU)

    2015-10-15

    Materials that undergo a conversion reaction with lithium (e.g., metal fluorides MF{sub 2}: M = Fe, Cu, ...) often accommodate more than one Li atom per transition-metal cation, and are promising candidates for high-capacity cathodes for lithium ion batteries. However, little is known about the mechanisms involved in the conversion process, the origins of the large polarization during electrochemical cycling, and why some materials are reversible (e.g., FeF{sub 2}) while others are not (e.g., CuF{sub 2}). In this study, we investigated the conversion reaction of binary metal fluorides, FeF{sub 2} and CuF{sub 2}, using a series of local and bulk probes to better understand the mechanisms underlying their contrasting electrochemical behavior. X-ray pair-distribution-function and magnetization measurements were used to determine changes in short-range ordering, particle size and microstructure, while high-resolution transmission electron microscopy (TEM) and electron energy-loss spectroscopy (EELS) were used to measure the atomic-level structure of individual particles and map the phase distribution in the initial and fully lithiated electrodes. Both FeF{sub 2} and CuF{sub 2} react with lithium via a direct conversion process with no intercalation step, but there are differences in the conversion process and final phase distribution. During the reaction of Li{sup +} with FeF{sub 2}, small metallic iron nanoparticles (<5 nm in diameter) nucleate in close proximity to the converted LiF phase, as a result of the low diffusivity of iron. The iron nanoparticles are interconnected and form a bicontinuous network, which provides a pathway for local electron transport through the insulating LiF phase. In addition, the massive interface formed between nanoscale solid phases provides a pathway for ionic transport during the conversion process. These results offer the first experimental evidence explaining the origins of the high lithium reversibility in FeF{sub 2}. In contrast

  6. Exploring 3D microstructural evolution in Li-Sulfur battery electrodes using in-situ X-ray tomography

    Science.gov (United States)

    Yermukhambetova, Assiya; Tan, Chun; Daemi, Sohrab R.; Bakenov, Zhumabay; Darr, Jawwad A.; Brett, Daniel J. L.; Shearing, Paul R.

    2016-10-01

    Lithium sulfur (Li-S) batteries offer higher theoretical specific capacity, lower cost and enhanced safety compared to current Li-ion battery technology. However, the multiple reactions and phase changes in the sulfur conversion cathode result in highly complex phenomena that significantly impact cycling life. For the first time to the authors’ knowledge, a multi-scale 3D in-situ tomography approach is used to characterize morphological parameters and track microstructural evolution of the sulfur cathode across multiple charge cycles. Here we show the uneven distribution of the sulfur phase fraction within the electrode thickness as a function of charge cycles, suggesting significant mass transport limitations within thick-film sulfur cathodes. Furthermore, we report a shift towards larger particle sizes and a decrease in volume specific surface area with cycling, suggesting sulfur agglomeration. Finally, we demonstrate the nano-scopic length-scale required for the features of the carbon binder domain to become discernible, confirming the need for future work on in-situ nano-tomography. We anticipate that X-ray tomography will be a powerful tool for optimization of electrode structures for Li-S batteries.

  7. Three dimensional Graphene aerogels as binder-less, freestanding, elastic and high-performance electrodes for lithium-ion batteries

    Science.gov (United States)

    Chen, Zhihang; Li, Hua; Tian, Ran; Duan, Huanan; Guo, Yiping; Chen, Yujie; Zhou, Jie; Zhang, Chunmei; DUGNANI, Roberto; Liu, Hezhou

    2016-01-01

    In this work it is shown how porous graphene aerogels fabricated by an eco-friendly and simple technological process, could be used as electrodes in lithium- ion batteries. The proposed graphene framework exhibited excellent performance including high reversible capacities, superior cycling stability and rate capability. A significantly lower temperature (75 °C) than the one currently utilized in battery manufacturing was utilized for self-assembly hence providing potential significant savings to the industrial production. After annealing at 600 °C, the formation of Sn-C-O bonds between the SnO2 nanoparticles and the reduced graphene sheets will initiate synergistic effect and improve the electrochemical performance. The XPS patterns revealed the formation of Sn-C-O bonds. Both SEM and TEM imaging of the electrode material showed that the three dimensional network of graphene aerogels and the SnO2 particles were distributed homogeneously on graphene sheets. Finally, the electrochemical properties of the samples as active anode materials for lithium-ion batteries were tested and examined by constant current charge–discharge cycling and the finding fully described in this manuscript. PMID:27265146

  8. Three dimensional Graphene aerogels as binder-less, freestanding, elastic and high-performance electrodes for lithium-ion batteries

    Science.gov (United States)

    Chen, Zhihang; Li, Hua; Tian, Ran; Duan, Huanan; Guo, Yiping; Chen, Yujie; Zhou, Jie; Zhang, Chunmei; Dugnani, Roberto; Liu, Hezhou

    2016-06-01

    In this work it is shown how porous graphene aerogels fabricated by an eco-friendly and simple technological process, could be used as electrodes in lithium- ion batteries. The proposed graphene framework exhibited excellent performance including high reversible capacities, superior cycling stability and rate capability. A significantly lower temperature (75 °C) than the one currently utilized in battery manufacturing was utilized for self-assembly hence providing potential significant savings to the industrial production. After annealing at 600 °C, the formation of Sn-C-O bonds between the SnO2 nanoparticles and the reduced graphene sheets will initiate synergistic effect and improve the electrochemical performance. The XPS patterns revealed the formation of Sn-C-O bonds. Both SEM and TEM imaging of the electrode material showed that the three dimensional network of graphene aerogels and the SnO2 particles were distributed homogeneously on graphene sheets. Finally, the electrochemical properties of the samples as active anode materials for lithium-ion batteries were tested and examined by constant current charge-discharge cycling and the finding fully described in this manuscript.

  9. Si–Cu alloy nanowires grown by oblique angle deposition as a stable negative electrode for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Polat, B. D.; Keles, O.; Chen, Z. H.; Amine, K.

    2016-03-29

    Thin films having nanocolumnar arrays made of various Si–Cu atomic ratios (90–10, 80–20, 70–30 %) are fabricated by an ion-assisted oblique angle co-deposition technique to produce stable negative electrodes for lithium-ion batteries. Cu is added into the electrode because of its ductility and electron conductivity. Cu plays a crucial role in holding the electrode together, minimizing overall capacity loss and enabling faster electron transfer. Plus, Cu is inactive versus Li?; therefore, Si–Cu variation is expected to affect the electrochemical performances of the electrodes. In this work, the effect of Si–Cu atomic ratios on the morphologies and the structures of the electrodes are studied. Plus, the uses of these nanocolumns with different Cu contents are evaluated as anodes by electrochemical tests. The morphological analyses demonstrate that an increase in Si–Cu atomic ratio affects the width of the nanocolumns and the homogeneity of the thin film morphology. The increase in Cu content dramatically improves the capacity retention of Si–Cu anodes, whereas it decreases the initial discharge capacity.

  10. High performance screen-printed electrodes prepared by a green solvent approach for lithium-ion batteries

    Science.gov (United States)

    Gören, A.; Mendes, J.; Rodrigues, H. M.; Sousa, R. E.; Oliveira, J.; Hilliou, L.; Costa, C. M.; Silva, M. M.; Lanceros-Méndez, S.

    2016-12-01

    New inks based on lithium iron phosphate and graphite for cathode and anode, respectively, were developed for printable lithium-ion batteries using the "green solvent" N,N‧-dimethylpropyleneurea (DMPU) and poly(vinylidene fluoride), PVDF, as a binder. The results were compared with the ones from inks developed with the conventionally used solvent N-methyl-2-pyrrolidone, NMP. The rheological properties of the PVDF/DMPU binder solution shows a more pronounced shear thinning behavior than the PVDF/NMP solution. Cathode inks prepared with 2.25 mL and 2.50 mL of DMPU for 1 g of electrode mass show an apparent viscosity of 3 Pa s and 2 Pa s for a shear rate of 100 s-1, respectively, being therefore processable by screen-printing or doctor blade techniques. The electrodes prepared with DMPU and processed by screen-printing show a capacity of 52 mAh g-1 at 2C for the cathode and 349 mAh g-1 at C/5 for the anode, after 45 charge-discharge cycles. The electrochemical performance of both electrodes was evaluated in a full-cell and after 9 cycles, the discharge capacity value is 81 mAh g-1, showing a discharge capacity retention of 64%. The new inks presented in this work are thus suitable for the development of printed batteries and represent a step forward towards more environmental friendly processes.

  11. Preliminary study on zinc-air battery using zinc regeneration electrolysis with propanol oxidation as a counter electrode reaction

    Science.gov (United States)

    Wen, Yue-Hua; Cheng, Jie; Ning, Shang-Qi; Yang, Yu-Sheng

    A zinc-air battery using zinc regeneration electrolysis with propanol oxidation as a counter electrode reaction is reported in this paper. It possesses functions of both zincate reduction and electrochemical preparation, showing the potential for increasing the electronic energy utilization. Charge/discharge tests and scanning electron microscopy (SEM) micrographs reveal that when a nickel sheet plated with the high-H 2-overpotential metal, cadmium, was used as the negative substrate electrode, the dendritic formation and hydrogen evolution are suppressed effectively, and granular zinc deposits become larger but relatively dense with the increase of charge time. The performance of batteries is favorable even if the charge time is as long as 5 h at the current density of 20 mA cm -2. Better discharge performance is achieved using a 'cavity-opening' configuration for the discharge cell rather than a 'gas-introducing' configuration. The highest energy efficiency is up to 59.2%. That is, the energy consumed by organic electro-synthesis can be recovered by 59.2%. Cyclic voltammograms show that the sintered nickel electrode exhibits a good electro-catalysis activity for the propanol oxidation. The increase of propanol concentration conduces to an enhancement in the organic electro-synthesis efficiency. The organic electro-synthesis current efficiency of 82% can be obtained.

  12. A Long-Life Lithium Ion Battery with Enhanced Electrode/Electrolyte Interface by Using an Ionic Liquid Solution.

    Science.gov (United States)

    Elia, Giuseppe Antonio; Ulissi, Ulderico; Mueller, Franziska; Reiter, Jakub; Tsiouvaras, Nikolaos; Sun, Yang-Kook; Scrosati, Bruno; Passerini, Stefano; Hassoun, Jusef

    2016-05-10

    In this paper, we report an advanced long-life lithium ion battery, employing a Pyr14 TFSI-LiTFSI non-flammable ionic liquid (IL) electrolyte, a nanostructured tin carbon (Sn-C) nanocomposite anode, and a layered LiNi1/3 Co1/3 Mn1/3 O2 (NMC) cathode. The IL-based electrolyte is characterized in terms of conductivity and viscosity at various temperatures, revealing a Vogel-Tammann-Fulcher (VTF) trend. Lithium half-cells employing the Sn-C anode and NMC cathode in the Pyr14 TFSI-LiTFSI electrolyte are investigated by galvanostatic cycling at various temperatures, demonstrating the full compatibility of the electrolyte with the selected electrode materials. The NMC and Sn-C electrodes are combined into a cathode-limited full cell, which is subjected to prolonged cycling at 40 °C, revealing a very stable capacity of about 140 mAh g(-1) and retention above 99 % over 400 cycles. The electrode/electrolyte interface is further characterized through a combination of electrochemical impedance spectroscopy (EIS) and scanning electron microscopy (SEM) investigations upon cell cycling. The remarkable performances reported here definitively indicate that IL-based lithium ion cells are suitable batteries for application in electric vehicles.

  13. Studies on two classes of positive electrode materials for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wilcox, James Douglas [Univ. of California, Berkeley, CA (United States)

    2008-12-01

    The development of advanced lithium-ion batteries is key to the success of many technologies, and in particular, hybrid electric vehicles. In addition to finding materials with higher energy and power densities, improvements in other factors such as cost, toxicity, lifetime, and safety are also required. Lithium transition metal oxide and LiFePO4/C composite materials offer several distinct advantages in achieving many of these goals and are the focus of this report. Two series of layered lithium transition metal oxides, namely LiNi1/3Co1/3-yMyMn1/3O2 (M=Al, Co, Fe, Ti) and LiNi0.4Co0.2-yMyMn0.4O2 (M = Al, Co, Fe), have been synthesized. The effect of substitution on the crystal structure is related to shifts in transport properties and ultimately to the electrochemical performance. Partial aluminum substitution creates a high-rate positive electrode material capable of delivering twice the discharge capacity of unsubstituted materials. Iron substituted materials suffer from limited electrochemical performance and poor cycling stability due to the degradation of the layered structure. Titanium substitution creates a very high rate positive electrode material due to a decrease in the anti-site defect concentration. LiFePO4 is a very promising electrode material but suffers from poor electronic and ionic conductivity. To overcome this, two new techniques have been developed to synthesize high performance LiFePO4/C composite materials. The use of graphitization catalysts in conjunction with pyromellitic acid leads to a highly graphitic carbon coating on the surface of LiFePO4 particles. Under the proper conditions, the room temperature electronic conductivity can be improved by nearly five orders of magnitude over untreated materials. Using Raman spectroscopy, the improvement in conductivity and rate performance of

  14. A binder-free sulfur/reduced graphene oxide aerogel as high performance electrode materials for lithium sulfur batteries

    Science.gov (United States)

    Nitze, Florian; Agostini, Marco; Lundin, Filippa; Palmqvist, Anders E. C.; Matic, Aleksandar

    2016-12-01

    Societies’ increasing need for energy storage makes it necessary to explore new concepts beyond the traditional lithium ion battery. A promising candidate is the lithium-sulfur technology with the potential to increase the energy density of the battery by a factor of 3–5. However, so far the many problems with the lithium-sulfur system have not been solved satisfactory. Here we report on a new approach utilizing a self-standing reduced graphene oxide based aerogel directly as electrodes, i.e. without further processing and without the addition of binder or conducting agents. We can thereby disrupt the common paradigm of “no battery without binder” and can pave the way to a lithium-sulfur battery with a high practical energy density. The aerogels are synthesized via a one-pot method and consist of more than 2/3 sulfur, contained inside a porous few-layered reduced graphene oxide matrix. By combining the graphene-based aerogel cathode with an electrolyte and a lithium metal anode, we demonstrate a lithium-sulfur cell with high areal capacity (more than 3 mAh/cm2 after 75 cycles), excellent capacity retention over 200 cycles and good sulfur utilization. Based on this performance we estimate that the energy density of this concept-cell can significantly exceed the Department of Energy (DEO) 2020-target set for transport applications.

  15. Fabrication of ordered NiO coated Si nanowire array films as electrodes for a high performance lithium ion battery.

    Science.gov (United States)

    Qiu, M C; Yang, L W; Qi, X; Li, Jun; Zhong, J X

    2010-12-01

    Highly ordered NiO coated Si nanowire array films are fabricated as electrodes for a high performance lithium ion battery via depositing Ni on electroless-etched Si nanowires and subsequently annealing. The structures and morphologies of as-prepared films are characterized by X-ray diffraction, scanning electron microscopy, and transmission electron microscopy. When the potential window versus lithium was controlled, the coated NiO can be selected to be electrochemically active to store and release Li+ ions, while highly conductive crystalline Si cores function as nothing more than a stable mechanical support and an efficient electrical conducting pathway. The hybrid nanowire array films exhibit superior cyclic stability and reversible capacity compared to that of NiO nanostructured films. Owing to the ease of large-scale fabrication and superior electrochemical performance, these hybrid nanowire array films will be promising anode materials for high performance lithium-ion batteries.

  16. High-performance graphene/sulphur electrodes for flexible Li-ion batteries using the low-temperature spraying method

    Science.gov (United States)

    Kumar, Pushpendra; Wu, Feng-Yu; Hu, Lung-Hao; Ali Abbas, Syed; Ming, Jun; Lin, Chia-Nan; Fang, Jason; Chu, Chih-Wei; Li, Lain-Jong

    2015-04-01

    Elementary sulphur (S) has been shown to be an excellent cathode material in energy storage devices such as Li-S batteries owing to its very high capacity. The major challenges associated with the sulphur cathodes are structural degradation, poor cycling performance and instability of the solid-electrolyte interphase caused by the dissolution of polysulfides during cycling. Tremendous efforts made by others have demonstrated that encapsulation of S materials improves their cycling performance. To make this approach practical for large scale applications, the use of low-cost technology and materials has become a crucial and new focus of S-based Li-ion batteries. Herein, we propose to use a low temperature spraying process to fabricate graphene/S electrode material, where the ink is composed of graphene flakes and the micron-sized S particles prepared by grinding of low-cost S powders. The S particles are found to be well hosted by highly conductive graphene flakes and consequently superior cyclability (~70% capacity retention after 250 cycles), good coulombic efficiency (~98%) and high capacity (~1500 mA h g-1) are obtained. The proposed approach does not require high temperature annealing or baking; hence, another great advantage is to make flexible Li-ion batteries. We have also demonstrated two types of flexible batteries using sprayed graphene/S electrodes.Elementary sulphur (S) has been shown to be an excellent cathode material in energy storage devices such as Li-S batteries owing to its very high capacity. The major challenges associated with the sulphur cathodes are structural degradation, poor cycling performance and instability of the solid-electrolyte interphase caused by the dissolution of polysulfides during cycling. Tremendous efforts made by others have demonstrated that encapsulation of S materials improves their cycling performance. To make this approach practical for large scale applications, the use of low-cost technology and materials has become

  17. Crystallographic origin of cycle decay of the high-voltage LiNi0.5Mn1.5O4 spinel lithium-ion battery electrode.

    Science.gov (United States)

    Pang, Wei Kong; Lu, Cheng-Zhang; Liu, Chia-Erh; Peterson, Vanessa K; Lin, Hsiu-Fen; Liao, Shih-Chieh; Chen, Jin-Ming

    2016-06-29

    High-voltage spinel LiNi0.5Mn1.5O4 (LNMO) is considered a potential high-power-density positive electrode for lithium-ion batteries, however, it suffers from capacity decay after extended charge-discharge cycling, severely hindering commercial application. Capacity fade is thought to occur through the significant volume change of the LNMO electrode occurring on cycling, and in this work we use operando neutron powder diffraction to compare the structural evolution of the LNMO electrode in an as-assembled 18650-type battery containing a Li4Ti5O12 negative electrode with that in an identical battery following 1000 cycles at high-current. We reveal that the capacity reduction in the battery post cycling is directly proportional to the reduction in the maximum change of the LNMO lattice parameter during its evolution. This is correlated to a corresponding reduction in the MnO6 octahedral distortion in the spinel structure in the cycled battery. Further, we find that the rate of lattice evolution, which reflects the rate of lithium insertion and removal, is ∼9 and ∼10% slower in the cycled than in the as-assembled battery during the Ni(2+)/Ni(3+) and Ni(3+)/Ni(4+) transitions, respectively.

  18. Effect of Electrode Dimensionality and Morphology on the Performance of Cu2Sb Thin Film Electrodes for Li-Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Trahey, Lynn; Kung, Harold H; Thackeray, Michael; Vaughey, John T.

    2011-08-09

    Although graphitic carbons have been commercially used in lithium-ion batteries for many years, their low crystallographic density limits their use in applications where space is at a premium. Among the alternative anode materials being considered for these applications are Zintl phases and intermetallic insertion anodes. Historically, main-group-metal-based anode materials have had problems with respect to volume expansion experienced on lithiation and its effect on cycle life. In this paper, we report the role of morphology and electrode dimensionality in extending the cycle life of the intermetallic insertion anode Cu₂Sb. We have found that controlling the surface area of the active material and building internal volume into the electrode structure significantly decreases the capacity fade on cycling. The decrease in fade rate may be due to the active material gradient identified within the structure produced by the electrodeposition process. This enhancement in cycling can be attributed to keeping the displaced copper closer to the active particles and to reducing the diffusion distances within the electrode.

  19. Facile synthetic route towards nanostructured Fe–TiO2(B), used as negative electrode for Li-ion batteries

    OpenAIRE

    Grosjean, Remi; Fehse, Marcus; Pigeot-Remy, Stéphanie; Stievano, Lorenzo; Monconduit, Laure; Cassaignon, Sophie

    2015-01-01

    International audience; We present here a novel simple method for the synthesis of highly pure TiO2(B). The fast microwave-assisted synthetic route allows facile scale-up of the process. Aiming at an application of the titania polymorph as negative electrode for Li-ion batteries, we have prepared a Fe-containing TiO2(B) and tested the electrochemical performances of both pure and Fe-containing materials. Fe insertion in TiO2(B) allows enhancing capacity and rate capability.

  20. Bio-mass derived mesoporous carbon as superior electrode in all vanadium redox flow battery with multicouple reactions

    Science.gov (United States)

    Ulaganathan, Mani; Jain, Akshay; Aravindan, Vanchiappan; Jayaraman, Sundaramurthy; Ling, Wong Chui; Lim, Tuti Mariana; Srinivasan, Madapusi P.; Yan, Qingyu; Madhavi, Srinivasan

    2015-01-01

    We first report the multi-couple reaction in all vanadium redox flow batteries (VRFB) while using bio-mass (coconut shell) derived mesoporous carbon as electrode. The presence of V3+/V4+ redox couple certainly supplies the additional electrons for the electrochemical reaction and subsequently provides improved electrochemical performance of VRFB system. The efficient electro-catalytic activity of such coconut shell derived high surface area mesoporous carbon is believed for the improved cell performance. Extensive power and electrochemical studies are performed for VRFB application point of view and described in detail.

  1. Self-assembly of virus-structured high surface area nanomaterials and their application as battery electrodes.

    Science.gov (United States)

    Royston, Elizabeth; Ghosh, Ayan; Kofinas, Peter; Harris, Michael T; Culver, James N

    2008-02-05

    High area nickel and cobalt surfaces were assembled using modified Tobacco mosaic virus (TMV) templates. Rod-shaped TMV templates (300 x 18 nm) engineered to encode unique cysteine residues were self-assembled onto gold patterned surfaces in a vertically oriented fashion, producing a >10-fold increase in surface area. Electroless deposition of ionic metals onto surface-assembled virus templates produced uniform metal coatings up to 40 nm in thickness. Within a nickel-zinc battery system, the incorporation of virus-assembled electrode surfaces more than doubled the total electrode capacity. When combined, these findings demonstrate that surface-assembled virus templates provide a robust platform for the fabrication of oriented high surface area materials.

  2. A flexible sulfur-graphene-polypropylene separator integrated electrode for advanced Li-S batteries.

    Science.gov (United States)

    Zhou, Guangmin; Li, Lu; Wang, Da-Wei; Shan, Xu-Yi; Pei, Songfeng; Li, Feng; Cheng, Hui-Ming

    2015-01-27

    A flexible Li-S battery based on an integrated structure of sulfur and graphene on a separator is developed. The internal graphene current collector offers a continuous conductive pathway, a modified interface with sulfur, and a good barrier to and an effective reservoir for dissolved polysulfides, consequently improving the capacity and cyclic life of the Li-S battery.

  3. Iron titanium phosphates as high-specific-capacity electrode materials for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Essehli, R., E-mail: essehli.rachid@yahoo.fr [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); ESECO SYSTEMS 270 rue Thomas Edison, Atelier Relais No 6, 34400 Lunel (France); El Bali, B. [Laboratory of Mineral Solid and Analytical Chemistry (LMSAC), Department of Chemistry, Faculty of Sciences, University Mohamed I, PO. Box 717, 60000 Oujda (Morocco); Faik, A. [CIC energigune, Parque Tecnológico de Álava, Albert Einstein 48, 01510 Miñano, Álava (Spain); Naji, M. [CNRS, UPR3079 CEMHTI, 1D avenue de la Recherche Scientifique, 45071 Orléans cedex 2 (France); Benmokhtar, S. [LCPGM, Laboratoire de Chimie-Physique Générale des Matériaux, Département de Chimie, Université Hassan II-Mohammedia, Faculté des Sciences Ben M’Sik, Casablanca (Morocco); Zhong, Y.R.; Su, L.W.; Zhou, Z. [Institute of New Energy Material Chemistry, Synergetic Innovation Center of Chemical Science and Engineering (Tianjin), Nankai University, Tianjin 300071 (China); Kim, J.; Kang, K. [Department of Materials Science and Engineering, Seoul National University, Gwanak-ro, Gwanak-gu, Seoul 151-742 (Korea, Republic of); Dusek, M. [Institute of Physics of the ASCR, v.v.i., Na Slovance 2, 182 21 Praha 8 (Czech Republic)

    2014-02-05

    Highlights: • Iron Titanium Phosphates as High-Specific-Capacity. • Electrode Materials for Lithium ion Batteries. • During the following cycles, good reversible capacity retention and better cyclabilit. • Ex-situ XRD analysis during the first discharge shows an amorphization of this anode material. -- Abstract: Two iron titanium phosphates, Fe{sub 0.5}TiOPO{sub 4} and Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3}, were prepared, and their crystal structures and electrochemical performances were compared. The electrochemical measurements of Fe{sub 0.5}TiOPO{sub 4} as an anode of a lithium ion cell showed that upon the first discharge down to 0.5 V, the cell delivered a capacity of 560 mA h/g, corresponding to the insertion of 5 Li’s per formula unit Fe{sub 0.5}TiOPO{sub 4}. Ex-situ XRD reveals a gradual evolution of the structure during cycling of the material, with lower crystallinity after the first discharge cycle. By correlating the electrochemical performances with the structural studies, new insights are achieved into the electrochemical behaviour of the Fe{sub 0.5}TiOPO{sub 4} anode material, suggesting a combination of intercalation and conversion reactions. The Nasicon-type Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} consists of a three-dimensional network made of corners and edges sharing [TiO{sub 6}] and [FeO{sub 6}] octahedra and [PO{sub 4}] tetrahedra leading to the formation of trimmers [FeTi{sub 2}O{sub 12}]. The first discharge of lithium ion cells based on Fe{sub 0.5}Ti{sub 2}(PO{sub 4}){sub 3} materials showed electrochemical activity of Ti{sup 4+}/Ti{sup 3+} and Fe{sup 2+}/Fe{sup 0} couples in the 2.5–1 V region. Below this voltage, the discharge profiles are typical of phosphate systems where Li{sub 3}PO{sub 4} is a product of the electrochemical reaction with lithium; moreover, the electrolyte solvent is reduced. An initial capacities as high as 1100 mA h g{sup −1} can be obtained at deep discharge. However, there is an irreversible capacity

  4. In situ scanning tunneling microscopy studies of the SEI formation on graphite electrodes for Li+-ion batteries

    Science.gov (United States)

    Seidl, Lukas; Martens, Slađana; Ma, Jiwei; Stimming, Ulrich; Schneider, Oliver

    2016-07-01

    The SEI-formation on graphitic electrodes operated as an Li+-ion battery anode in a standard 1 M LiPF6 EC/DMC (1 : 1) electrolyte has been studied in situ by EC-STM. Two different modes of in situ study were applied, one, which allowed to follow topographic and crystallographic changes (solvent cointercalation, graphite exfoliation, SEI precipitation on the HOPG basal plane) of the graphite electrode during SEI-formation, and the second, which gave an insight into the SEI precipitation on the HOPG basal plane in real time. From the in situ EC-STM studies, not only conclusions about the SEI-topography could be drawn, but also about the formation mechanism and the chemical composition, which strongly depend on the electrode potential. It was shown that above 1.0 V vs. Li/Li+ the SEI-formation is still reversible, since the molecular structure of the solvent molecules remains intact during an initial reduction step. During further reduction, the molecular structures of the solvents are destructed, which causes the irreversible charge loss. The STM studies were completed by electrochemical methods, like cyclic voltammetry, the potentiostatic intermittent titration technique and charge/discharge tests of MCMB electrodes.

  5. Leaching lithium from the anode electrode materials of spent lithium-ion batteries by hydrochloric acid (HCl).

    Science.gov (United States)

    Guo, Yang; Li, Feng; Zhu, Haochen; Li, Guangming; Huang, Juwen; He, Wenzhi

    2016-05-01

    Spent lithium-ion batteries (LIBs) are considered as an important secondary resource for its high contents of valuable components, such as lithium and cobalt. Currently, studies mainly focus on the recycling of cathode electrodes. There are few studies concentrating on the recovery of anode electrodes. In this work, based on the analysis result of high amount of lithium contained in the anode electrode, the acid leaching process was applied to recycle lithium from anode electrodes of spent LIBs. Hydrochloric acid was introduced as leaching reagent, and hydrogen peroxide as reducing agent. Within the range of experiment performed, hydrogen peroxide was found to have little effect on lithium leaching process. The highest leaching recovery of 99.4wt% Li was obtained at leaching temperature of 80°C, 3M hydrochloric acid and S/L ratio of 1:50g/ml for 90min. The graphite configuration with a better crystal structure obtained after the leaching process can also be recycled.

  6. Amorphous Li-Al-Based Compounds: A Novel Approach for Designing High Performance Electrode Materials for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Franziska Thoss

    2013-11-01

    Full Text Available A new amorphous compound with the initial atomic composition Al43Li43Y6Ni8 applied as electrode material for Li-ion batteries is investigated. Unlike other amorphous compounds so-far investigated as anode materials, it already contains Li as a base element in the uncycled state. The amorphous compound powder is prepared by high energy ball milling of a master alloy. It shows a strongly enhanced specific capacity in contrast to amorphous alloys without Li in the initial state. Therewith, by enabling a reversible (delithiation of metallic electrodes without the phase transition caused volume changes it offers the possibility of much increased specific capacities than conventional graphite anodes. According to the charge rate (C-rate, the specific capacity is reversible over 20 cycles at minimum in contrast to conventional crystalline intermetallic phases failing by volume changes. The delithiation process occurs quasi-continuously over a voltage range of nearly 4 V, while the lithiation is mainly observed between 0.1 V and 1.5 V. That way, the electrode is applicable for different potential needs. The electrode stays amorphous during cycling, thus avoiding volume changes. The cycling performance is further enhanced by a significant amount of Fe introduced as wear debris from the milling tools, which acts as a promoting element.

  7. Vertically aligned N-doped coral-like carbon fiber arrays as efficient air electrodes for high-performance nonaqueous Li-O2 batteries.

    Science.gov (United States)

    Shui, Jianglan; Du, Feng; Xue, Chenming; Li, Quan; Dai, Liming

    2014-03-25

    High energy efficiency and long cycleability are two important performance measures for Li-air batteries. Using a rationally designed oxygen electrode based on a vertically aligned nitrogen-doped coral-like carbon nanofiber (VA-NCCF) array supported by stainless steel cloth, we have developed a nonaqueous Li-O2 battery with an energy efficiency as high as 90% and a narrow voltage gap of 0.3 V between discharge/charge plateaus. Excellent reversibility and cycleability were also demonstrated for the newly developed oxygen electrode. The observed outstanding performance can be attributed to its unique vertically aligned, coral-like N-doped carbon microstructure with a high catalytic activity and an optimized oxygen/electron transportation capability, coupled with the microporous stainless steel substrate. These results demonstrate that highly efficient and reversible Li-O2 batteries are feasible by using a rationally designed carbon-based oxygen electrode.

  8. Ab initio study of radiation effects on the Li4Ti5O12 electrode used in lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Adib Samin

    2015-04-01

    Full Text Available Lithium-ion batteries are currently in wide use owing to their high energy density and enhanced capabilities. Li4Ti5O12 is a promising anode material for lithium-ion batteries because of its advantageous properties. Lithium-ion batteries could be exposed to radiation occurring in various conditions such as during outer space exploration and nuclear accidents. In this study, we apply density functional theory to explore the effect of radiation damage on this electrode and, ultimately, on the performance of the battery. It was found that radiation could affect the structural stability of the material. Furthermore, the electrode was shown to undergo a transition from insulator to metal, following the defects due to radiation. In addition, the effect of radiation on the intercalation potential was found to be highly dependent on the nature of the defect induced.

  9. The performance of Ebonex ® electrodes in bipolar lead-acid batteries

    Science.gov (United States)

    Ellis, Keith; Hill, Andrew; Hill, John; Loyns, Andrew; Partington, Tom

    Recent work by Atraverda on the production of an Ebonex ® material that can be cheaply formulated and manufactured to form bipolar substrate plates for bipolar lead-acid batteries is described. In addition, data obtained by Atraverda from laboratory lead-acid batteries is presented indicating that weight savings of around 40% for a bipolar 36 V design (20 Ah capacity, 5 h rate, 9 kW) are potentially achievable in comparison to more conventional designs containing monopolar lead grids. Results indicate that their use as bipolar substrate materials will provide light-weight, long-lasting lead-acid batteries suitable for automotive, standby and power tool applications.

  10. High-rate, long-life Ni-Sn nanostructured electrodes for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Hassoun, J.; Panero, S.; Scrosati, B. [Department of Chemistry, University of Rome ' ' La Sapienza' ' , P.le Aldo Moro 5, 00185 Rome (Italy); Simon, P.; Taberna, P.L. [CIRIMAT-UMR 5085 - Universite Paul Sabatier, route de Narbonne, 31062 Toulouse, Cedex 4 (France)

    2007-06-18

    Ni{sub 3}Sn{sub 4} intermetallic electrodes prepared into a revolutionary nanostructure, obtained by electrodeposition on a nanoarchitectured Cu substrate, are described. This structure controls the volume stress that accompanies the electrochemical process yielding a performance rarely observed with lithium metal storage electrodes. The new electrode shows impressive electrochemical behavior and cycles in lithium cells for more than 200 cycles with a stable high capacity. (Abstract Copyright [2007], Wiley Periodicals, Inc.)

  11. Olivine electrode engineering impact on the electrochemical performance of lithium-ion batteries.

    Energy Technology Data Exchange (ETDEWEB)

    Lu, W.; Jansen, A.; Dees, D.; Henriksen, G.; Chemical Sciences and Engineering Division

    2010-08-01

    High energy and power density lithium iron phosphate was studied for hybrid electric vehicle applications. This work addresses the effects of porosity in a composite electrode using a four-point probe resistivity analyzer, galvanostatic cycling, and electrochemical impedance spectroscopy (EIS). The four-point probe result indicates that the porosity of composite electrode affects the electronic conductivity significantly. This effect is also observed from the cell's pulse current discharge performance. Compared to the direct current (dc) methods used, the EIS data are more sensitive to electrode porosity, especially for electrodes with low porosity values.

  12. A finite element simulation on transient large deformation and mass diffusion in electrodes for lithium ion batteries

    Science.gov (United States)

    An, Yonghao; Jiang, Hanqing

    2013-10-01

    Lithium-ion batteries have attracted great deal of attention recently. Silicon is one of the most promising anode materials for high-performance lithium-ion batteries, due to its highest theoretical specific capacity. However, the short lifetime confined by mechanical failure in the silicon anode is now considered to be the biggest challenge in desired applications. High stress induced by the huge volume change due to lithium insertion/extraction is the main reason underlying this problem. Some theoretical models have been developed to address this issue. In order to properly implement these models, we develop a finite element based numerical method using a commercial software package, ABAQUS, as a platform at the continuum level to study fully coupled large deformation and mass diffusion problem. Using this method, large deformation, elasticity-plasticity of the electrodes, various spatial and temporal conditions, arbitrary geometry and dimension could be fulfilled. The interaction between anode and other components of the lithium ion batteries can also be studied as an integrated system. Several specific examples are presented to demonstrate the capability of this numerical platform.

  13. Atomic and Molecular Layer Deposition for Enhanced Lithium Ion Battery Electrodes and Development of Conductive Metal Oxide/Carbon Composites

    Science.gov (United States)

    Travis, Jonathan

    The performance and safety of lithium-ion batteries (LIBs) are dependent on interfacial processes at the positive and negative electrodes. For example, the surface layers that form on cathodes and anodes are known to affect the kinetics and capacity of LIBs. Interfacial reactions between the electrolyte and the electrodes are also known to initiate electrolyte combustion during thermal runaway events that compromise battery safety. Atomic layer deposition (ALD) and molecular layer deposition (MLD) are thin film deposition techniques based on sequential, self-limiting surface reactions. ALD and MLD can deposit ultrathin and conformal films on high aspect ratio and porous substrates such as composite particulate electrodes in lithium-ion batteries. The effects of electrode surface modification via ALD and MLD are studied using a variety of techniques. It was found that sub-nm thick coatings of Al2O 3 deposited via ALD have beneficial effects on the stability of LIB anodes and cathodes. These same Al2O3 ALD films were found to improve the safety of graphite based anodes through prevention of exothermic solid electrolyte interface (SEI) degradation at elevated temperatures. Ultrathin and conformal metal alkoxide polymer films known as "metalcones" were grown utilizing MLD techniques with trimethylaluminum (TMA) or titanium tetrachloride (TiCl4) and organic diols or triols, such as ethylene glycol (EG), glycerol (GL) or hydroquinone (HQ), as the reactants. Pyrolysis of these metalcone films under inert gas conditions led to the development of conductive metal oxide/carbon composites. The composites were found to contain sp2 carbon using micro-Raman spectroscopy in the pyrolyzed films with pyrolysis temperatures ≥ 600°C. Four point probe measurements demonstrated that the graphitic sp2 carbon domains in the metalcone films grown using GL and HQ led to significant conductivity. The pyrolysis of conformal MLD films to obtain conductive metal oxide/carbon composite films

  14. Nano-structures Enhanced Novel Composite Electrode Material for Batteries Project

    Data.gov (United States)

    National Aeronautics and Space Administration — Integrate advanced nanotechnology with energy storage technology to develop advanced cathode material for use in Li-ion batteries while maintaining high level of...

  15. Complementary X-ray and neutron radiography study of the initial lithiation process in lithium-ion batteries containing silicon electrodes

    Science.gov (United States)

    Sun, Fu; Markötter, Henning; Manke, Ingo; Hilger, André; Alrwashdeh, Saad S.; Kardjilov, Nikolay; Banhart, John

    2017-03-01

    Complementary in operando X-ray radiography and neutron radiography measurements were conducted to investigate and visualize the initial lithiation in silicon-electrode lithium-ion batteries. By means of X-ray radiography, a significant volume expansion of Si particles and the Si electrode during the first discharge was observed. In addition, many Si particles were found that never undergo electrochemical reactions. These findings were confirmed by neutron radiography, which, for the first time, showed the process of Li alloying with the Si electrode during initial lithiation. These results demonstrate that complementary X-ray and neutron radiography is a powerful tool to investigate the lithiation mechanisms inside Si-electrode based lithium-ion batteries.

  16. Graphite as negative electrode in Li-ion batteries; Le graphite comme electrode negative dans les accumulateurs Li-ion

    Energy Technology Data Exchange (ETDEWEB)

    Fischer, F.; Monnier, A. [Timcal SA (France)

    1996-12-31

    The last developments in lithium batteries design have demonstrated the advantages of graphite: competitive cost, flat output curve, high capacity thanks to the obtention of a final compound close to LiC{sub 6}, good behaviour during cycling and a high mass energy. However, these advantages are slightly tarnished by parasite secondary reactions during the evolution of the element. Two different cases are encountered: the formation of a passivation layer (loss of Li ions and formation of irreversible bounds) and the formation of a passivation layer with a reaction between graphite and the solvent (partial destruction of the graphite crystal lattice). In the first case, the theoretical graphite insertion capacity remains at 372 mAh/g while in the second case the insertion capacity is greatly reduced. Abstract only. (J.S.)

  17. Etched colloidal LiFePO4 nanoplatelets toward high-rate capable Li-ion battery electrodes.

    Science.gov (United States)

    Paolella, Andrea; Bertoni, Giovanni; Marras, Sergio; Dilena, Enrico; Colombo, Massimo; Prato, Mirko; Riedinger, Andreas; Povia, Mauro; Ansaldo, Alberto; Zaghib, Karim; Manna, Liberato; George, Chandramohan

    2014-12-10

    LiFePO4 has been intensively investigated as a cathode material in Li-ion batteries, as it can in principle enable the development of high power electrodes. LiFePO4, on the other hand, is inherently "plagued" by poor electronic and ionic conductivity. While the problems with low electron conductivity are partially solved by carbon coating and further by doping or by downsizing the active particles to nanoscale dimensions, poor ionic conductivity is still an issue. To develop colloidally synthesized LiFePO4 nanocrystals (NCs) optimized for high rate applications, we propose here a surface treatment of the NCs. The particles as delivered from the synthesis have a surface passivated with long chain organic surfactants, and therefore can be dispersed only in aprotic solvents such as chloroform or toluene. Glucose that is commonly used as carbon source for carbon-coating procedure is not soluble in these solvents, but it can be dissolved in water. In order to make the NCs hydrophilic, we treated them with lithium hexafluorophosphate (LiPF6), which removes the surfactant ligand shell while preserving the structural and morphological properties of the NCs. Only a roughening of the edges of NCs was observed due to a partial etching of their surface. Electrodes prepared from these platelet NCs (after carbon coating) delivered a capacity of ∼ 155 mAh/g, ∼ 135 mAh/g, and ∼ 125 mAh/g, at 1 C, 5 C, and 10 C, respectively, with significant capacity retention and remarkable rate capability. For example, at 61 C (10.3 A/g), a capacity of ∼ 70 mAh/g was obtained, and at 122 C (20.7 A/g), the capacity was ∼ 30 mAh/g. The rate capability and the ease of scalability in the preparation of these surface-treated nanoplatelets make them highly suitable as electrodes in Li-ion batteries.

  18. Tin transition metal carbon alloys for lithium-ion battery negative electrodes

    Science.gov (United States)

    Todd, Andrew Douglas William

    Tin-transition metal (for M = Ti, V, Cr, Mn, Fe, Co, Ni, and Cu) and tin-transition metal-carbon (for M = Ti, V and Co) alloys were studied using combinatorial materials science techniques and high throughput characterization methods to identify the optimum transition metal to use as an alloy for Li-ion battery negative electrodes. Amorphous composition ranges were found in the Sn-Ti, Sn-V, Sn-Cr, and Sn-Co systems with the amorphous range forming with the lowest concentration of transition metal for Co. No composition from the Sn-M systems showed stable charge-discharge cycling. Of the tin-transition metal-carbon alloys studied, it was determined that the Sn-Co-C system had compositions for which the charge-discharge cycling was stable and the specific capacities were close to 600 mAh/g. It is speculated that the Sn-Co-C system remains amorphous over many charge-discharge cycles because of a lack of stable, room temperature Co-carbides. Mossbauer effect spectroscopy was performed on a Sn1-xCo x library and a [Sn0.63Co0.37]1- yCy library to help understand the local environment of the tin atoms in these materials and it was determined that the carbon did not have a great effect. Small angle neutron scattering (SANS) measurements were used to compare Sn-Co-C materials produced by mechanical attriting to Sn-Co-C materials produced by sputter deposition. These results revealed differences in the nanostructure. The attrited [Sn0.5Co0.5]1- yCy (for y = 0, 0.1, 0.2, 0.3, 0.4, 0.5, 0.6, 0.7, and 0.8) materials were found to have a SnCo grain size on the order of 60 A while the sputtered [Sn0.45Co0.55 ]1-yCy (for y = 0.02, 0.10, 0.21, 0.34, 0.56, and 0.74) materials were found to be amorphous or have a SnCo grain size near 10 A, depending on composition. This difference in nanostructure may explain why the mechanically attrited samples could not attain their theoretical specific capacity while the sputtered samples were much closer to doing so. Porosity detected in the

  19. Quality control tool of electrode coating for lithium-ion batteries based on X-ray radiography

    Science.gov (United States)

    Etiemble, A.; Besnard, N.; Adrien, J.; Tran-Van, P.; Gautier, L.; Lestriez, B.; Maire, E.

    2015-12-01

    A simple and efficient method, based on X-ray radiography, is developed to check the quality (homogeneity of the thickness, presence of defects) of NMC-, LFP- and NMC/LFP-based electrode coating for Li-ion batteries at the scale of several cm2 with a resolution of 20 μm. As a first step, the attenuation coefficient of NMC- and LFP-based coating is experimentally determined according to the Beer-Lambert law. Then, the attenuation coefficient of each active material is estimated from these experimental results and X-ray attenuation databases, which allows establishing an attenuation law for any coating composition. Finally, thanks to this relationship, the thickness can be evaluated in each spot of the film and the defects, such as pinholes or broad edges with gradual decrease of the thickness coating, can be detected. The analysis of NMC-, LFP- and NMC/LFP-based electrodes shows that the coating quality decreases as coating thickness increases and as the nanometric vs. micrometric material content increases in the coating composition. This reveals detrimental aspects of nanomaterials with respect to their use in composite electrode manufactured through conventional slot-die or casting process.

  20. Resolving Losses at the Negative Electrode in All-Vanadium Redox Flow Batteries Using Electrochemical Impedance Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Che Nan [ORNL; Delnick, Frank M [ORNL; Aaron, D [University of Tennessee, Knoxville (UTK); Mench, Matthew M [ORNL; Zawodzinski, Thomas A [ORNL

    2014-01-01

    We present an in situ electrochemical technique for the quantitative measurement and resolution of the ohmic, charge transfer and diffusion overvoltages at the negative electrode of an all-vanadium redox flow battery (VRFB) using electrochemical impedance spectroscopy (EIS). The mathematics describing the complex impedance of the V+2/V+3 redox reaction is derived and matches the experimental data. The voltage losses contributed by each process have been resolved and quantified at various flow rates and electrode thicknesses as a function of current density during anodic and cathodic polarization. The diffusion overvoltage was affected strongly by flow rate while the charge transfer and ohmic losses were invariant. On the other hand, adopting a thicker electrode significantly changed both the charge transfer and diffusion losses due to increased surface area. Furthermore, the Tafel plot obtained from the impedance resolved charge transfer overvoltage yielded the geometric exchange current density, anodic and cathodic Tafel slopes (135 5 and 121 5 mV/decade respectively) and corresponding transfer coefficients = 0.45 0.02 and = 0.50 0.02 in an operating cell.

  1. Novel architecture of composite electrode for optimization of lithium battery performance

    Energy Technology Data Exchange (ETDEWEB)

    Guy, D.; Lestriez, B.; Gaudefroy, V.; Guyomard, D. [Laboratoire de Chimie des Solides, Institut des Materiaux Jean Rouxel, CNRS, Universite de Nantes, B.P. 32229, 44322 Nantes Cedex 3 (France); Bouchet, R. [Laboratoire Madirel, Universite de Marseille, Centre Sr Jerome, Av. Escadrille Normandie Niemen, 13397 Marseille Cedex 20 (France)

    2006-06-19

    We show that the polymeric binder of the composite electrode may have an important role on the lithium trivanadate Li{sub 1.2}V{sub 3}O{sub 8} electrode performance. We describe a new tailored polymeric binder combination with controlled polymer-filler (carbon black) interactions that allows the preparation of new and more efficient electrode architecture. Using this polymeric binder, composite electrodes based on Li{sub 1.2}V{sub 3}O{sub 8} display a room temperature cycling capacity of 280mAhg{sup -1} (C/5 rate, 3.3-2V) instead of 150mAhg{sup -1} using a standard-type (poly(vinylidene fluoride)-hexafluoropropylene (PVdF-HFP) binder) composite electrode. We have coupled scanning electron microscopy (SEM) observations, galvanostatic cycling and electrochemical impedance spectroscopy in order to define and understand the impact of the microstructure of the composite electrode on its electrochemical performance. Derived from these studies, the main key factors that provide efficient charge carrier collection within the composite electrode complex medium are discussed. (author)

  2. Interfacial behaviours between lithium ion conductors and electrode materials in various battery systems

    Energy Technology Data Exchange (ETDEWEB)

    Wu, Bingbin; Wang, Shanyu; Evans IV, Willie J.; Deng, Daniel Z.; Yang, Jihui; Xiao, Jie

    2016-01-01

    In recent years room temperature Li+ ion conductors have been intensively revisited in order to develop safe lithium ion (Li-ion) batteries and beyond that can be deployed in the electrical vehicles. Through careful modification on materials synthesis, promising solid Li+ conductors with high ionic conductivity, competitve with liquid electrolytes, have been demonstrated. However, the integration of those highly conductive solid electrolytes into the whole system is still very challenging mainly due to the high impedance existing in the different interfaces throughout the entire battery structure. Herein , this review paper focuses on the overview of the interfacial behaviors between Li+ conductors and cathode/anode materials. The origin, evolution and potential solutions to reuce these interfacial impedances are reviewed for various battery systems spanning from Li-ion, lithium sulfur (Li-S), lithium oxygen (Li-O2) batteries to lithium metal protection. The predicted gravimetric and volumetric energy densities at different scenarios are also discussed along with the prospectives for further development of solid state batteries.

  3. Laser printing and femtosecond laser structuring of electrode materials for the manufacturing of 3D lithium-ion micro-batteries

    Science.gov (United States)

    Smyrek, P.; Kim, H.; Zheng, Y.; Seifert, H. J.; Piqué, A.; Pfleging, W.

    2016-04-01

    Recently, three-dimensional (3D) electrode architectures have attracted great interest for the development of lithium-ion micro-batteries applicable for Micro-Electro-Mechanical Systems (MEMS), sensors, and hearing aids. Since commercial available micro-batteries are mainly limited in overall cell capacity by their electrode footprint, new processing strategies for increasing both capacity and electrochemical performance have to be developed. In case of such standard microbatteries, two-dimensional (2D) electrode arrangements are applied with thicknesses up to 200 μm. These electrode layers are composed of active material, conductive agent, graphite, and polymeric binder. Nevertheless, with respect to the type of active material, the active material to conductive agent ratio, and the film thickness, such thick-films suffer from low ionic and electronic conductivities, poor electrolyte accessibility, and finally, limited electrochemical performance under challenging conditions. In order to overcome these drawbacks, 3D electrode arrangements are under intense investigation since they allow the reduction of lithium-ion diffusion pathways in between inter-digitated electrodes, even for electrodes with enhanced mass loadings. In this paper, we present how to combine laser-printing and femtosecond laser-structuring for the development of advanced 3D electrodes composed of Li(Ni1/3Mn1/3Co1/3)O2 (NMC). In a first step, NMC thick-films were laser-printed and calendered to achieve film thicknesses in the range of 50 μm - 80 μm. In a second step, femtosecond laser-structuring was carried out in order to generate 3D architectures directly into thick-films. Finally, electrochemical cycling of laser-processed films was performed in order to evaluate the most promising 3D electrode designs suitable for application in long life-time 3D micro-batteries.

  4. Method of preparing graphene-sulfur nanocomposites for rechargeable lithium-sulfur battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Liu, Jun; Lemmon, John P; Yang, Zhenguo; Cao, Yuliang; Li, Xiaolin

    2015-04-07

    A method of preparing a graphene-sulfur nanocomposite for a cathode in a rechargeable lithium-sulfur battery comprising thermally expanding graphite oxide to yield graphene layers, mixing the graphene layers with a first solution comprising sulfur and carbon disulfide, evaporating the carbon disulfide to yield a solid nanocomposite, and grinding the solid nanocomposite to yield the graphene-sulfur nanocomposite. Rechargeable-lithium-sulfur batteries having a cathode that includes a graphene-sulfur nanocomposite can exhibit improved characteristics. The graphene-sulfur nanocomposite can be characterized by graphene sheets with particles of sulfur adsorbed to the graphene sheets. The sulfur particles have an average diameter of less than 50 nm.

  5. Molecular Layer Deposition for Surface Modification of Lithium-Ion Battery Electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Ban, Chunmei [Center of Chemistry and Nanoscience, National Renewable Energy Laboratory, Golden CO 80401 USA; George, Steven M. [Department of Chemistry and Biochemistry, University of Colorado at Boulder, Boulder CO 80309 USA; Department of Mechanical Engineering, University of Colorado at Boulder, Boulder CO 80309 USA

    2016-10-21

    Inspired by recent successes in applying molecular layer deposition (MLD) to stabilize lithium-ion (Li-ion) electrodes, this review presents the MLD process and its outstanding attributes for electrochemical applications. The review discusses various MLD materials and their implementation in Li-ion electrodes. The rationale behind these emerging uses of MLD is examined to motivate future efforts on the fundamental understanding of interphase chemistry and the development of new materials for enhanced electrochemical performance.

  6. A long-life lithium ion sulfur battery exploiting high performance electrodes.

    Science.gov (United States)

    Moreno, Noelia; Agostini, Marco; Caballero, Alvaro; Morales, Julián; Hassoun, Jusef

    2015-10-04

    A novel lithium ion sulfur battery is formed by coupling an activated ordered mesoporous carbon-sulfur (AOMC-S) cathode and a nanostructured tin-carbon anode. The lithium ion cell has improved reversibility, high energy content and excellent cycle life.

  7. Graphene-sulfur nanocomposites for rechargeable lithium-sulfur battery electrodes

    Science.gov (United States)

    Liu, Jun; Lemmon, John P; Yang, Zhenguo; Cao, Yuiliang; Li, Xiaolin

    2014-06-17

    Rechargeable lithium-sulfur batteries having a cathode that includes a graphene-sulfur nanocomposite can exhibit improved characteristics. The graphene-sulfur nanocomposite can be characterized by graphene sheets with particles of sulfur adsorbed to the graphene sheets. The sulfur particles have an average diameter less than 50 nm..

  8. New highly active oxygen reduction electrode for PEM fuel cell and Zn/air battery applications (NORA). Final report

    Energy Technology Data Exchange (ETDEWEB)

    Thiele, D.; Zuettel, A.

    2008-04-15

    This illustrated final report for the Swiss Federal Office of Energy (SFOE) presents the results of a project concerning a new, highly active oxygen reduction electrode for PEM fuel cell and zinc/air battery applications. The goal of this project was, according to the authors, to increase the efficiency of the oxygen reduction reaction by lowering the activation polarisation through the right choice of catalyst and by lowering the concentration polarisation. In this work, carbon nanotubes are used as support material. The use of these nanotubes grown on perovskites is discussed. Theoretical considerations regarding activation polarisation are discussed and alternatives to the use of platinum are examined. The results of experiments carried out are presented in graphical and tabular form. The paper is completed with a comprehensive list of references.

  9. Intercalation driven porosity effects on the electro-chemo-thermo-mechanical response in continuum models for battery material electrodes

    CERN Document Server

    Wang, Zhenlin; Garikipati, Krishna

    2016-01-01

    We present a coupled continuum formulation for the electrostatic, chemical, thermal and mechanical processes in battery materials. Our treatment applies on the macroscopic scale, at which electrodes can be modelled as porous materials made up of active particles held together by binders and perfused by the electrolyte. Starting with the description common to the field, in terms of reaction-transport partial differential equations for ions, variants of the classical Poisson equation for electrostatics, and the heat equation, we add mechanics to the problem. Our main contribution is to model the evolution of porosity as a consequence of strains induced by intercalation, thermal expansion and mechanical stresses. Recognizing the potential for large local deformations, we have settled on the finite strain framework. In this first communication we have carried out a detailed computational study on the influence of the dynamically evolving porosity, via the electrostatic and reaction-transport coefficients, upon io...

  10. Degradation of Li/S Battery Electrodes On 3D Current Collectors Studied Using X-ray Phase Contrast Tomography.

    Science.gov (United States)

    Zielke, L; Barchasz, C; Waluś, S; Alloin, F; Leprêtre, J-C; Spettl, A; Schmidt, V; Hilger, A; Manke, I; Banhart, J; Zengerle, R; Thiele, S

    2015-06-04

    Lithium/sulphur batteries are promising candidates for future energy storage systems, mainly due to their high potential capacity. However low sulphur utilization and capacity fading hinder practical realizations. In order to improve understanding of the system, we investigate Li/S electrode morphology changes for different ageing steps, using X-ray phase contrast tomography. Thereby we find a strong decrease of sulphur loading after the first cycle, and a constant loading of about 15% of the initial loading afterwards. While cycling, the mean sulphur particle diameters decrease in a qualitatively similar fashion as the discharge capacity fades. The particles spread, migrate into the current collector and accumulate in the upper part again. Simultaneously sulphur particles lose contact area with the conducting network but regain it after ten cycles because their decreasing size results in higher surface areas. Since the capacity still decreases, this regain could be associated with effects such as surface area passivation and increasing charge transfer resistance.

  11. Microwave-assisted preparation of carbon nanofiber-functionalized graphite felts as electrodes for polymer-based redox-flow batteries

    Science.gov (United States)

    Schwenke, A. M.; Janoschka, T.; Stolze, C.; Martin, N.; Hoeppener, S.; Schubert, U. S.

    2016-12-01

    A simple and fast microwave-assisted protocol to functionalize commercially available graphite felts (GFs) with carbon nanofibers (CNFs) for the application as electrode materials in redox-flow batteries (RFB) is demonstrated. As catalyst for the CNF synthesis nickel acetate is applied and ethanol serves as the carbon source. By the in-situ growth of CNFs, the active surface of the electrodes is increased by a factor of 50, which is determined by the electrochemical double layer capacities of the obtained materials. Furthermore, the morphology of the CNF-coating is investigated by scanning electron microscopy. Subsequently, the functionalized electrodes are applied in a polymer-based redox-flow battery (pRFB) using a TEMPO- and a viologen polymer as active materials. Due to the increased surface area as compared to an untreated graphite felt electrode, the current rating is improved by about 45% at 80 mA cm-2 and, furthermore, a decrease in overpotentials is observed. Thus, using this microwave-assisted synthesis approach, CNF-functionalized composite electrodes are prepared with a very simple protocol suitable for real life applications and an improvement of the overall performance of the polymer-based redox-flow battery is demonstrated.

  12. Stability of carbon electrodes for aqueous lithium-air secondary batteries

    Science.gov (United States)

    Ohkuma, Hirokazu; Uechi, Ichiro; Matsui, Masaki; Takeda, Yasuo; Yamamoto, Osamu; Imanishi, Nobuyuki

    2014-01-01

    The air electrode performance of various carbon materials, such as Ketjen black (KB), acetylene black (AB and AB-S), Vulcan XC-72R (VX), and vapor grown carbon fiber (VGCF) with and without La0.6Sr0.4Co0.2Fe0.8O3 (LSCF) catalyst were examined in an aqueous solution of saturated LiOH with 10 M LiCl in the current density range 0.2-2.0 mA cm-2. The best performance for oxygen reduction and evolution reactions was observed for the KB electrode, which has the highest surface area among the carbon materials examined. A steady over-potential of 0.2 V was obtained for the oxygen reduction reaction using the KB electrode without the catalyst, while the over-potential was 0.15 V for KB with the LSCF catalyst at 2.0 mA cm-2. The over-potentials for the oxygen evolution reaction were slightly higher than those for the oxygen reduction reaction, and gradually increased with the polarization period. Analysis of the gas in the cell after polarization above 0.4 V revealed the evolution of a small amount of CO during the oxygen evolution reaction by the decomposition of carbon in the electrode. The amount of CO evolved was significantly decreased by the addition of LSCF to the carbon electrode.

  13. Rechargeable aqueous lithium-air batteries with an auxiliary electrode for the oxygen evolution

    Science.gov (United States)

    Sunahiro, S.; Matsui, M.; Takeda, Y.; Yamamoto, O.; Imanishi, N.

    2014-09-01

    A rechargeable aqueous lithium-air cell with a third auxiliary electrode for the oxygen evolution reaction was developed. The cell consists of a lithium metal anode, a lithium conducting solid electrolyte of Li1+x+yAlx(Ti,Ge)2-xSiyP3-yO12, a carbon black oxygen reduction air electrode, a RuO2 oxygen evolution electrode, and a saturated aqueous solution of LiOH with 10 M LiCl. The cell was successfully operated for several cycles at 0.64 mA cm-2 and 25 °C under air, where the capacity of air electrode was 2000 mAh gcathod-1. The cell performance was degraded gradually by cycling under open air. The degradation was reduced under CO2-free air and pure oxygen. The specific energy density was calculated to be 810 Wh kg-1 from the weight of water, lithium, oxygen, and carbon in the air electrode.

  14. Iron-Air Rechargeable Battery

    Science.gov (United States)

    Narayan, Sri R. (Inventor); Prakash, G.K. Surya (Inventor); Kindler, Andrew (Inventor)

    2014-01-01

    Embodiments include an iron-air rechargeable battery having a composite electrode including an iron electrode and a hydrogen electrode integrated therewith. An air electrode is spaced from the iron electrode and an electrolyte is provided in contact with the air electrode and the iron electrodes. Various additives and catalysts are disclosed with respect to the iron electrode, air electrode, and electrolyte for increasing battery efficiency and cycle life.

  15. Silver nanoparticle-decorated carbon nanotubes as bifunctional gas-diffusion electrodes for zinc-air batteries

    Science.gov (United States)

    Wang, T.; Kaempgen, M.; Nopphawan, P.; Wee, G.; Mhaisalkar, S.; Srinivasan, M.

    Thin, lightweight, and flexible gas-diffusion electrodes (GDEs) based on freestanding entangled networks of single-walled carbon nanotubes (SWNTs) decorated with Ag nanoparticles (AgNPs) are tested as the air-breathing cathode in a zinc-air battery. The SWNT networks provide a highly porous surface for active oxygen absorption and diffusion. The high conductivity of SWNTs coupled with the catalytic activity of AgNPs for oxygen reduction leads to an improvement in the performance of the zinc-air cell. By modulating the pH value and the reaction time, different sizes of AgNPs are decorated uniformly on the SWNTs, as revealed by transmission electron microscopy and powder X-ray diffraction. AgNPs with sizes of 3-5 nm double the capacity and specific energy of a zinc-air battery as compared with bare SWNTs. The simplified, lightweight architecture shows significant advantages over conventional carbon-based GDEs in terms of weight, thickness and conductivity, and hence may be useful for mobile and portable applications.

  16. Hierarchical sulfur electrodes as a testing platform for understanding the high-loading capability of Li-S batteries

    Science.gov (United States)

    Chung, Sheng-Heng; Chang, Chi-Hao; Manthiram, Arumugam

    2016-12-01

    Lithium-sulfur (Li-S) batteries are considered as an attractive electrochemical energy storage system due to the high theoretical capacity of sulfur (1,675 mA h g-1). However, high-loading sulfur cathodes would need to be employed for the Li-S cells to be practical, but the resulting poor cell cyclability and severe electrode degradation hamper their development. Here, we present a hierarchical sulfur cathode as a testing platform for understanding the high-loading capability of Li-S batteries. The hierarchical cathode presents good electrochemical utilization of above 70%, stable cyclability for 500-1,000 cycles, and high sulfur loadings of 4.2-10.0 mg cm-2. The exploration of the activation and the polysulfide-retention processes of the high-loading cathodes illustrates that the electrochemical stability mainly results from the stabilization of dissolved polysulfides within the cathode region as the electrochemically active catholyte. Therefore, the utilization of stabilized polysulfide migration might be a meaningful opportunity for designing high-loading cathodes and further improving their electrochemical stability and long-term cyclability.

  17. Synthetic silver oxide and mercury-free zinc electrodes for silver-zinc reserve batteries

    Science.gov (United States)

    Smith, David F.; Gucinski, James A.

    Reserve activated silver oxide-zinc cells were constructed with synthetic silver oxide (Ag 2O) electrodes with Pb-treated zinc electrodes produced by a non-electrolytic process. The cells were tested before and after thermally accelerated aging. At discharge rates up to 80 mA cm -2, the discharge was limited by the Ag 2O electrode, with a coulombic efficiency between 89-99%. At higher rates, the cells are apparently zinc-limited. Test cells were artificially aged at 90°C for 19 h and discharged at 21°C at 80 mA cm -2. No capacity loss was measured, but a delayed activation rise time was noted (192 ms fresh vs. 567 ms aged). The delay is thought to be caused by zinc passivation due to the outgassing of cell materials.

  18. Double-plasma enhanced carbon shield for spatial/interfacial controlled electrodes in lithium ion batteries via micro-sized silicon from wafer waste

    Science.gov (United States)

    Chen, Bing-Hong; Chuang, Shang-I.; Duh, Jenq-Gong

    2016-11-01

    Using spatial and interfacial control, the micro-sized silicon waste from wafer slurry could greatly increase its retention potential as a green resource for silicon-based anode in lithium ion batteries. Through step by step spatial and interfacial control for electrode, the cyclability of recycled waste gains potential performance from its original poor retention property. In the stages of spatial control, the electrode stabilizers of active, inactive and conductive additives were mixed into slurries for maintaining architecture and conductivity of electrode. In addition, a fusion electrode modification of interfacial control combines electrolyte additive, technique of double-plasma enhanced carbon shield (D-PECS) to convert the chemical bond states and to alter the formation of solid electrolyte interphases (SEIs) in the first cycle. The depth profiles of chemical composition from external into internal electrode illustrate that the fusion electrode modification not only forms a boundary to balance the interface between internal and external electrodes but also stabilizes the SEIs formation and soothe the expansion of micro-sized electrode. Through these effect approaches, the performance of micro-sized Si waste electrode can be boosted from its serious capacity degradation to potential retention (200 cycles, 1100 mAh/g) and better meet the requirements for facile and cost-effective in industrial production.

  19. Alkylphosphate-based nonflammable gel electrolyte for LiMn 2O 4 positive electrode in lithium-ion battery

    Science.gov (United States)

    Yoshimoto, Nobuko; Gotoh, Daisuke; Egashira, Minato; Morita, Masayuki

    Polymeric gel containing alkylphosphate has been examined as nonflammable gel electrolyte for LiMn 2O 4 positive electrode of lithium-ion battery (LIB). The gel was composed of a polymer matrix of poly(vinylidenefluoride- co-hexafluoropropylene) (PVdF-HFP) and a liquid component consisting of ternary solvent of trimethyl phosphate (TMP) mixed with ethylene carbonate (EC) and diethyl carbonate (DEC) that dissolves lithium salt (LiPF 6 or LiBF 4). The gel composition of 0.8 M (mol dm -3) LiX (X = PF 6 and BF 4) dissolved in EC + DEC + TMP (55:25:20) with PVdF-HFP showed excellent nonflammable characteristics and high ionic conductivity of ca. 3.1 mS cm -1 at room temperature (20 °C). The charge-discharge cycling test of LiMn 2O 4 positive electrode gave good reversibility with high capacitance in the gel electrolyte. With respect to the electrolyte salt, LiBF 4 was better than LiPF 6 due to its thermal stability during the gel preparation.

  20. Improvement of the Performance of Graphite Felt Electrodes for Vanadium-Redox-Flow-Batteries by Plasma Treatment

    Directory of Open Access Journals (Sweden)

    Eva-Maria Hammer

    2014-02-01

    Full Text Available In the frame of the present contribution oxidizing plasma pretreatment is used for the improvement of the electrocatalytic activity of graphite felt electrodes for Vanadium-Redox-Flow-Batteries (VRB. The influence of the working gas media on the catalytic activity and the surface morphology is demonstrated. The electrocatalytical properties of the graphite felt electrodes were examined by cyclic voltammetry and electrochemical impedance spectroscopy. The obtained results show that a significant improvement of the redox reaction kinetics can be achieved for all plasma modified samples using different working gasses (Ar, N2 and compressed air in an oxidizing environment. Nitrogen plasma treatment leads to the highest catalytical activities at the same operational conditions. Through a variation of the nitrogen plasma treatment duration a maximum performance at about 14 min cm-2 was observed, which is also represented by a minimum of 90 Ω in the charge transfer resistance obtained by EIS measurements. The morphology changes of the graphitized surface were followed using SEM.

  1. Ultra-light Hierarchical Graphene Electrode for Binder-Free Supercapacitors and Lithium-Ion Battery Anodes.

    Science.gov (United States)

    Zuo, Zicheng; Kim, Tae Young; Kholmanov, Iskandar; Li, Huifeng; Chou, Harry; Li, Yuliang

    2015-10-01

    A mild and environmental-friendly method is developed for fabricating a 3D interconnected graphene electrode with large-scale continuity. Such material has interlayer pores between reduced graphene oxide nanosheets and in-plane pores. Hence, a specific surface area up to 835 m(2) g(-1) and a high powder conductivity up to 400 S m(-1) are achieved. For electrochemical applications, the interlayer pores can serve as "ion-buffering reservoirs" while in-plane ones act as "channels" for shortening the mass cross-plane diffusion length, reducing the ion response time, and prevent the interlayer restacking. As binder-free supercapacitor electrode, it delivers a specific capacitance up to 169 F g(-1) with surface-normalized capacitance close to 21 μF cm(-2) (intrinsic capacitance) and power density up to 7.5 kW kg(-1), in 6 m KOH aqueous electrolyte. In the case of lithium-ion battery anode, it shows remarkable advantages in terms of the initiate reversible Coulombic efficiency (61.3%), high specific capacity (932 mAh g(-1) at 100 mA g(-1)), and robust long-term retention (93.5% after 600 cycles at 2000 mAh g(-1)).

  2. USE OF BATTERY CARBON AS ELECTRODES IN ARC DISCHARGE METHOD FOR FABRICATION OF CARBON-MODIFIED TIO2

    Directory of Open Access Journals (Sweden)

    Isya Fitria Andhika

    2016-09-01

    Full Text Available Fabrication with carbon-modified TiO2 by arc discharge method in liquid medium has been studied. This research was performed in two steps including fabrication and characterization. This fabrication was done by arcdischarge method with graphite electrodes from dry cell batteries and liquid medium suspension of TiO2 in ethanol 30, 50 and 70 %. A strong current was applied to electrode as 10 -50 A (20-40 V. Nanocomposites formed on the liquid medium surface were collected and characterized using X-ray diffraction (XRD,scanning electron microscope (SEM dan energy dispersive spectroscopy (EDS to determine crystallinity, surface morphology and the constituent elements, respectively. XRD data shows that the most effective fabrication TiO2/Karbon by liquid medium in ethanol 50 % indicated from the formation of a new peak with high intensity of TiC on 2Ɵ= 36.02 °. SEM data shows that the morphology of each aggregated TiO2/Karbon compared to the morphology of TiO2. In addition, EDS data shows the presence of the element carbon, titanium and oxygen in the same area indicating that the successful formation of composite material between TiO2 dan carbon.

  3. Bismuth Nanoparticle Decorating Graphite Felt as a High-Performance Electrode for an All-Vanadium Redox Flow Battery

    Energy Technology Data Exchange (ETDEWEB)

    Li, Bin; Gu, Meng; Nie, Zimin; Shao, Yuyan; Luo, Qingtao; Wei, Xiaoliang; Li, Xiaolin; Xiao, Jie; Wang, Chong M.; Sprenkle, Vincent L.; Wang, Wei

    2013-02-04

    The selection of electrode materials plays a great role in improving performances of all vanadium redox flow batteries (VRBs). Low-cost graphite felt (GF) as traditional electrode material has to be modified to address its issue of low electrocatalytic activity. In our paper, low-cost and highly conductive bismuth nanoparticles, as a powerful alternative electrocatalyst to noble metal, are proposed and synchronously electro-deposited onto the surface of GF while running flow cells employing the electrolytes containing suitable Bi3+. Although bismuth is proved to only take effect on the redox reaction of V(II)/V(III) and present at negative half-cell side, the whole cell electrochemical performances are significantly improved. In particular, the energy efficiency is increased by 11% owing to faster charge transfer as compared with one without Bi at high charge/discharge rate of 150 mA/cm2, which is prone to reduce stack size, thus dramatically reducing the cost. The excellent results show great promise of Bi nano-catalysts in the commercialization of VRBs in terms of product cost as well as electrochemical properties.

  4. Conductive Polymer Binder for High-Tap-Density Nanosilicon Material for Lithium-Ion Battery Negative Electrode Application.

    Science.gov (United States)

    Zhao, Hui; Wei, Yang; Qiao, Ruimin; Zhu, Chenhui; Zheng, Ziyan; Ling, Min; Jia, Zhe; Bai, Ying; Fu, Yanbao; Lei, Jinglei; Song, Xiangyun; Battaglia, Vincent S; Yang, Wanli; Messersmith, Phillip B; Liu, Gao

    2015-12-09

    High-tap-density silicon nanomaterials are highly desirable as anodes for lithium ion batteries, due to their small surface area and minimum first-cycle loss. However, this material poses formidable challenges to polymeric binder design. Binders adhere on to the small surface area to sustain the drastic volume changes during cycling; also the low porosities and small pore size resulting from this material are detrimental to lithium ion transport. This study introduces a new binder, poly(1-pyrenemethyl methacrylate-co-methacrylic acid) (PPyMAA), for a high-tap-density nanosilicon electrode cycled in a stable manner with a first cycle efficiency of 82%-a value that is further improved to 87% when combined with graphite material. Incorporating the MAA acid functionalities does not change the lowest unoccupied molecular orbital (LUMO) features or lower the adhesion performance of the PPy homopolymer. Our single-molecule force microscopy measurement of PPyMAA reveals similar adhesion strength between polymer binder and anode surface when compared with conventional polymer such as homopolyacrylic acid (PAA), while being electronically conductive. The combined conductivity and adhesion afforded by the MAA and pyrene copolymer results in good cycling performance for the high-tap-density Si electrode.

  5. Electrochemical modification of a pyrolytic graphite sheet for improved negative electrode performance in the vanadium redox flow battery

    Science.gov (United States)

    Kabir, Humayun; Gyan, Isaiah O.; Francis Cheng, I.

    2017-02-01

    The vanadium redox flow battery is a promising technology for buffering renewable energies. It is recognized that negative electrode is the limitation in this device where there are problems of slow heterogeneous electron transfer (HET) of V3+/2+ and parasitic H2 evolution. Any methods aimed at addressing one of these barriers must assess the effects on the other. We examine electrochemical enhancement of a common commercially available material. Treatment of Panasonic pyrolytic graphite sheets is through oxidation at 2.1 V vs. Ag/AgCl for 1 min in 1 M H2SO4. This increases the standard HET rate for V3+/2+ from 3.2 × 10-7 to 1 × 10-3 cm/s, one of the highest in literature and shifts voltammetric reductive peak potential from -1.0 V to -0.65 V in 50 mM V3+ in 1 M H2SO4. Infrared analysis of the surfaces indicates formation of Csbnd OH, Cdbnd O, and Csbnd O functionalities. These groups catalyze HET with V3+/2+ as hypothesized by Skyllas-Kasacos. Also of significance is that electrode modification decreases the fraction of the current directed towards H2 evolution. This proportion decreases by two orders of a magnitude from 12% to 0.1% as measured at the respective voltammetric peak potentials of -1.0 V (pristine) and -0.65 V (modified).

  6. Virus-Assembled Flexible Electrode-Electrolyte Interfaces for Enhanced Polymer-Based Battery Applications

    OpenAIRE

    Ayan Ghosh; Juchen Guo; Brown, Adam D.; Elizabeth Royston; Chunsheng Wang; Peter Kofinas; James N. Culver

    2012-01-01

    High-aspect-ratio cobalt-oxide-coated Tobacco mosaic virus (TMV-) assembled polytetrafluoroethylene (PTFE) nonstick surfaces were integrated with a solvent-free polymer electrolyte to create an anode-electrolyte interface for use in lithium-ion batteries. The virus-assembled PTFE surfaces consisted primarily of cobalt oxide and were readily intercalated with a low-molecular-weight poly (ethylene oxide) (PEO) based diblock copolymer electrolyte to produce a solid anode-electrolyte system. The ...

  7. Improved Mechanical Integrity of ALD-Coated Composite Electrodes for Li-Ion Batteries

    Science.gov (United States)

    2011-01-01

    potential of these coatings for high-energy density Li-ion batteries suitable for vehicular applications. © 2010 The Electrochemical Society . DOI: 10.1149...and 80 mN, and the complete delami- * Electrochemical Society Student Member. ** Electrochemical Society Active member. z E-mail: Anne.dillon@nrel.gov...28.00 © The Electrochemical Society A29 Downloaded 23 Dec 2010 to 24.9.104.47. Redistribution subject to ECS license or copyright; see http

  8. Electrode materials for lithium-ion batteries characterized by electrochemical impedance spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Schweikert, N.; Indris, S. [Karlsruher Institut fuer Technologie (KIT), Karlsruhe (Germany); Krueger, S.; Roling, B. [Marburg Univ. (Germany)

    2010-07-01

    In order to characterize the electrochemical properties of Li{sub 4}Ti{sub 5}O{sub 12} electrochemical impedance spectroscopy (EIS) was used. Long-term measurements were performed in order to identify interfacial reactions, loss mechanisms and degradation processes. By performing impedance measurements at different Li contents, the dependency on the state-of-charge (SOC) of the Li/Li{sub 4+x}Ti{sub 5}O{sub 12} battery was investigated. (orig.)

  9. Proposal of simple and novel method of capacity fading analysis using pseudo-reference electrode in lithium ion cells: Application to solvent-free lithium ion polymer batteries

    Science.gov (United States)

    Shono, Kumi; Kobayashi, Takeshi; Tabuchi, Masato; Ohno, Yasutaka; Miyashiro, Hajime; Kobayashi, Yo

    2014-02-01

    We propose a simple procedure for introducing a pseudo-reference electrode (PRE) to lithium ion batteries using isometric lithium metal placed between the cathode and anode, and we successfully obtained the cathode and anode voltage profiles, individual interfacial impedances, and the misalignment of the operation range between the cathode and anode after cycle operation. The proposed procedure is applicable to lithium ion battery systems using a solid electrolyte to prepare two cells with a lithium counter electrode. We determined the capacity decrease of a solvent-free lithium ion polymer battery consisting of a LiNi1/3Mn1/3Co1/3O2 (NMC), a polyether-based solid polymer electrolyte (SPE), and a graphite (Gr) with the proposed PRE over 1000 cycles. The capacity retention of the [Gr|SPE|NMC] cell reached 50% at the 1000th cycle upon the optimization of cell preparation, and we found that the main factor of the capacity decrease was the continuous irreversible loss of active lithium at the graphite anode, not the oxidation of the SPE. Our findings suggest that we should reconsider combining a polyether-based SPE with a conventionally used 4 V class cathode and a graphite anode to develop an innovative, safe, and low-cost battery for the expected large lithium ion battery systems for stationary use.

  10. Carbon-based air electrodes carrying MnO 2 in zinc-air batteries

    Science.gov (United States)

    Wei, Zidong; Huang, Wenzhang; Zhang, Shengtao; Tan, Jun

    Catalysts prepared from the carbon black impregnated with manganous nitrate solution and then heated at temperature from 270°C to 450°C were investigated. It was found that the impregnated catalysts heated at temperature of 340°C exhibited the best catalytic activity for oxygen reduction in alkaline electrolyte. It was also found that the XRD spectra of pyrolytic MnO 2 from manganous nitrate over 340°C were different from those below 340°C. The enhanced catalysis of air electrodes was ascribed to the formation of MnO 2 crystal with d-value of 2.72 Å as the impregnated-catalysts was heated at temperature of 340°C. The other factors in preparation of air electrodes were also discussed.

  11. Carbon nanotubes functionalized by salts containing stereogenic heteroatoms as electrodes in their battery cells

    Directory of Open Access Journals (Sweden)

    Zdanowska Sandra

    2016-12-01

    Full Text Available This paper concentrates on electrochemical properties of groups of multi-walled carbon nanotubes (MWCNT functionalized with substituents containing a stereogenic heteroatom bonded covalently to the surface of the carbon nanotube. This system was tested in Swagelok-type cells. The cells comprised a system (functionalized CNT with salts containing S and P atoms with a working electrode, microfiber separators soaked with electrolyte solution, and a lithium foil counter/reference (commercial LiCoO2 electrode. The electrolyte solution was 1 M LiPF6 in propylene carbonate. Using standard techniques (cyclic voltammetry/chronopotentiometry, galvanostatic cycling was performed on the cells at room temperature with a CH Instruments Model 600E potentiostat/galvanostat electrochemical measurements. Methods of functionalization CNT were compared in terms of the electrochemical properties of the studied systems. In all systems, the process of charge/discharge was observed.

  12. Nanoscience Supporting the Research on the Negative Electrodes of Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Alain Mauger

    2015-12-01

    Full Text Available Many efforts are currently made to increase the limited capacity of Li-ion batteries using carbonaceous anodes. The way to reach this goal is to move to nano-structured material because the larger surface to volume ratio of particles and the reduction of the electron and Li path length implies a larger specific capacity. Additionally, nano-particles can accommodate such a dilatation/contraction during cycling, resulting in a calendar life compatible with a commercial use. In this review attention is focused on carbon, silicon, and Li4Ti5O12 materials, because they are the most promising for applications.

  13. Lithium Storage Mechanisms in Purpurin Based Organic Lithium Ion Battery Electrodes

    Science.gov (United States)

    2012-12-11

    elucidated using NMR, UV and FTIR spectral studies. The formation of the most favored six membered binding core of lithium ion with carbonyl groups of purpurin...purpurin, which has been extracted from a common plant Madder, most often used as a dye for fabrics. The extracted and chemically lithiated purpurin...proposed based on detailed NMR spectral analysis of the lithiated purpurin electrode (ELP) as well as CLP, and were supported by UV-vis and FTIR studies

  14. Disulfide-Bridged (Mo3S11) Cluster Polymer: Molecular Dynamics and Application as Electrode Material for a Rechargeable Magnesium Battery.

    Science.gov (United States)

    Truong, Quang Duc; Kempaiah Devaraju, Murukanahally; Nguyen, Duc N; Gambe, Yoshiyuki; Nayuki, Keiichiro; Sasaki, Yoshikazu; Tran, Phong D; Honma, Itaru

    2016-09-14

    Exploring novel electrode materials is critical for the development of a next-generation rechargeable magnesium battery with high volumetric capacity. Here, we showed that a distinct amorphous molybdenum sulfide, being a coordination polymer of disulfide-bridged (Mo3S11) clusters, has great potential as a rechargeable magnesium battery cathode. This material provided good reversible capacity, attributed to its unique structure with high flexibility and capability of deformation upon Mg insertion. Free-terminal disulfide moiety may act as the active site for reversible insertion and extraction of magnesium.

  15. Electrochemical performance of electroless nickel plated silicon electrodes for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Cetinkaya, T., E-mail: tcetinkaya@sakarya.edu.tr; Uysal, M.; Akbulut, H.

    2015-04-15

    Highlights: • Si/Ni composite powders were produced via electroless plating method. • Increasing content of the nickel on the surface of the silicon powders caused increasing discharge capacity. • The Si/Ni composite electrode produced using 40 g/L NiCl{sub 2} exhibited 246 mAh/g discharge capacity after 30 cycles. - Abstract: In this study, nickel plated silicon powders were produced using an electroless deposition process. The nickel content on the surface of silicon powders was changed by using different concentrations of NiCl{sub 2} in the plating bath. The surface morphology of the produced Ni plated composite powders was characterized using scanning electron microscopy (SEM). Energy dispersive spectroscopy (EDS) was used to determine the elemental surface composition of the composites. X-ray diffraction (XRD) analysis was performed to investigate the structure of the nickel plated silicon powders. Electrochemical cycling test of the nickel plated silicon electrodes were performed at a constant current of 100 mA/g in CR2016 test cells. In order to investigate electrochemical reactions of the nickel plated silicon powders with electrolyte, cyclic voltammetry test was performed at a scan rate of 0.1 mV/s. Among the used concentrations, the nickel plated silicon electrode produced using 40 g/L NiCl{sub 2} had a 246 mAh/g discharge capacity after 30 cycles.

  16. Synergistic effect of carbon nanofiber/nanotube composite catalyst on carbon felt electrode for high-performance all-vanadium redox flow battery.

    Science.gov (United States)

    Park, Minjoon; Jung, Yang-jae; Kim, Jungyun; Lee, Ho il; Cho, Jeaphil

    2013-10-01

    Carbon nanofiber/nanotube (CNF/CNT) composite catalysts grown on carbon felt (CF), prepared from a simple way involving the thermal decomposition of acetylene gas over Ni catalysts, are studied as electrode materials in a vanadium redox flow battery. The electrode with the composite catalyst prepared at 700 °C (denoted as CNF/CNT-700) demonstrates the best electrocatalytic properties toward the V(2+)/V(3+) and VO(2+)/VO2(+) redox couples among the samples prepared at 500, 600, 700, and 800 °C. Moreover, this composite electrode in the full cell exhibits substantially improved discharge capacity and energy efficiency by ~64% and by ~25% at 40 mA·cm(-2) and 100 mA·cm(-2), respectively, compared to untreated CF electrode. This outstanding performance is due to the enhanced surface defect sites of exposed edge plane in CNF and a fast electron transfer rate of in-plane side wall of the CNT.

  17. Tapioca binder for porous zinc anodes electrode in zinc–air batteries

    Directory of Open Access Journals (Sweden)

    Mohamad Najmi Masri

    2015-07-01

    Full Text Available Tapioca was used as a binder for porous Zn anodes in an electrochemical zinc-air (Zn-air battery system. The tapioca binder concentrations varied to find the optimum composition. The effect of the discharge rate at 100 mA on the constant current, current–potential and current density–power density of the Zn-air battery was measured and analyzed. At concentrations of 60–80 mg cm−3, the tapioca binder exhibited the optimum discharge capability, with a specific capacity of approximately 500 mA h g−1 and a power density of 17 mW cm−2. A morphological analysis proved that at this concentration, the binder is able to provide excellent binding between the Zn powders. Moreover, the structure of Zn as the active material was not affected by the addition of tapioca as the binder, as shown by the X-ray diffraction analysis. Furthermore, the conversion of Zn into ZnO represents the full utilization of the active material, which is a good indication that tapioca can be used as the binder.

  18. Electrode and solid electrolyte thin films for secondary lithium-ion batteries

    Science.gov (United States)

    Chen, C. H.; Kelder, E. M.; Schoonman, J.

    Electrostatic spray deposition (ESD) was employed to prepare thin layers of Li 1.2Mn 2O 4 (nominal composition) and BPO 4:0.035Li 2O for all-solid-state thin film lithium-ion batteries. The relationships between layer morphologies and deposition conditions such as solvent composition of the precursor solutions and substrate temperature were investigated. It was found that a low substrate temperature and/or high boiling point of the solvent may lead to a relatively dense structure. Reticular porous structures are formed, if films were deposited at 250°C and a mixture of 85 vol.% butyl carbitol and 15 vol.% ethanol was used as the solvent. The Li 1.2Mn 2O 4 layers, formed in the 250-400°C temperature range, were amorphous or micro-crystalline. After annealing beyond 600 °C, they could be crystallized into a spinel-structured material. Glassy BPO 4:0.035Li 2O layers could fill the pores of porous Li 1.2Mn 2O 4 layers to form a dense intermediate electrolyte layer. Thin-film rocking-chair batteries, Li 1.2Mn 2O 4|BPO 4:0.035Li 2O|Li 1.2Mn 2O 4|Al, were prepared and revealed an open-circuit voltage of about 1.2 V after charging.

  19. Mesoporous Li4Ti5O12 nanoclusters anchored on super-aligned carbon nanotubes as high performance electrodes for lithium ion batteries

    Science.gov (United States)

    Sun, Li; Kong, Weibang; Wu, Hengcai; Wu, Yang; Wang, Datao; Zhao, Fei; Jiang, Kaili; Li, Qunqing; Wang, Jiaping; Fan, Shoushan

    2015-12-01

    Mesoporous lithium titanate (LTO) nanoclusters are in situ synthesized in a network of super aligned carbon nanotubes (SACNTs) via a solution-based method followed by heat treatment in air. In the LTO-CNT composite, SACNTs not only serve as the skeleton to support a binder-free electrode, but also render the composite with high conductivity, flexibility, and mechanical strength. The homogeneously dispersed LTO nanoclusters among the SACNTs allow each LTO grain to effectively access the electrolyte and the conductive network, benefiting both ion and electron transport. By the incorporation of LTO into the CNT network, mechanical reinforcement is also achieved. When serving as a negative electrode for lithium ion batteries, such a robust composite-network architecture provides the electrodes with effective charge transport and structural integrity, leading to high-performance flexible electrodes with high capacity, high rate capability, and excellent cycling stability.Mesoporous lithium titanate (LTO) nanoclusters are in situ synthesized in a network of super aligned carbon nanotubes (SACNTs) via a solution-based method followed by heat treatment in air. In the LTO-CNT composite, SACNTs not only serve as the skeleton to support a binder-free electrode, but also render the composite with high conductivity, flexibility, and mechanical strength. The homogeneously dispersed LTO nanoclusters among the SACNTs allow each LTO grain to effectively access the electrolyte and the conductive network, benefiting both ion and electron transport. By the incorporation of LTO into the CNT network, mechanical reinforcement is also achieved. When serving as a negative electrode for lithium ion batteries, such a robust composite-network architecture provides the electrodes with effective charge transport and structural integrity, leading to high-performance flexible electrodes with high capacity, high rate capability, and excellent cycling stability. Electronic supplementary information

  20. Hydrogen diffusion in La{sub 1.5}Nd{sub 0.5}MgNi{sub 9} alloy electrodes of the Ni/MH battery

    Energy Technology Data Exchange (ETDEWEB)

    Volodin, A.A. [Institute of Problems of Chemical Physics of RAS, Chernogolovka (Russian Federation); Denys, R.V. [Institute for Energy Technology, P.O. Box 40, Kjeller NO2027 (Norway); Tsirlina, G.A. [Department of Electrochemistry, Moscow State University, Moscow (Russian Federation); Tarasov, B.P. [Institute of Problems of Chemical Physics of RAS, Chernogolovka (Russian Federation); Fichtner, M. [Institute of Nanotechnology, Karlsruhe Institute of Technology, Karlsruhe (Germany); Yartys, V.A., E-mail: volodymyr.yartys@ife.no [Institute for Energy Technology, P.O. Box 40, Kjeller NO2027 (Norway)

    2015-10-05

    Highlights: • Hydrogen diffusion in the La{sub 1.5}Nd{sub 0.5}MgNi{sub 9} alloy electrode was studied. • Various techniques of low amplitude potentiostatic data treatment were used. • D{sub H} demonstrates a maximum (2 × 10{sup −11} cm{sup 2}/s) at 85% of discharge of the electrode. • Maximum is associated with a conversion of β-hydride into a solid α-solution. • Optimization of material and electrode will allow high discharge rates. - Abstract: Hydrogen diffusion in the La{sub 1.5}Nd{sub 0.5}MgNi{sub 9} battery electrode material has been studied using low amplitude potentiostatic experiments. Complex diffusion behavior is examined in frames of electroanalytical models proposed for the lithium intercalation materials. Hydrogen diffusion coefficient D{sub H} changes with hydrogen content in the metal hydride anode electrode and has a maximum of ca. 2 × 10{sup −11} cm{sup 2}/s at ca. 85% of discharge. Such a behavior differs from the trends known for the transport in lithium battery materials, but qualitatively agrees with the data for the highly concentrated β-PdH{sub x}.

  1. LiFePO 4 water-soluble binder electrode for Li-ion batteries

    Science.gov (United States)

    Guerfi, A.; Kaneko, M.; Petitclerc, M.; Mori, M.; Zaghib, K.

    A new water-soluble elastomer from ZEON Corp. was evaluated as binder with LiFePO 4 cathode material in Li-ion batteries. The mechanical characteristic of this cathode was compared to that with PVdF-based cathode binder. The elastomer-based cathode shows high flexibility with good adhesion. The electrochemical performance was also evaluated and compared to PVdF-based cathodes at 25 and at 60 °C. A lower irreversible capacity loss was obtained with the elastomer-based cathode, however, aging at 60 °C shows a comparable cycle life to that observed with PVdF-based cathodes. The LiFePO 4-WSB at high rate shows a good performance with 120 mAh g -1 at 10 C rate at 60 °C.

  2. LiFePO{sub 4} water-soluble binder electrode for Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Guerfi, A.; Petitclerc, M.; Zaghib, K. [Institut de Recherche d' Hydro-Quebec, 1800 Lionel-Boulet, Varennes, Que. J3X 1S1 (Canada); Kaneko, M.; Mori, M. [ZEON Corporation, R and D Center, 1-2-1 Yako, Kawasaki, Kanagawa 210-9507 (Japan)

    2007-01-01

    A new water-soluble elastomer from ZEON Corp. was evaluated as binder with LiFePO{sub 4} cathode material in Li-ion batteries. The mechanical characteristic of this cathode was compared to that with PVdF-based cathode binder. The elastomer-based cathode shows high flexibility with good adhesion. The electrochemical performance was also evaluated and compared to PVdF-based cathodes at 25 and at 60{sup o}C. A lower irreversible capacity loss was obtained with the elastomer-based cathode, however, aging at 60{sup o}C shows a comparable cycle life to that observed with PVdF-based cathodes. The LiFePO{sub 4}-WSB at high rate shows a good performance with 120mAhg{sup -1} at 10C rate at 60{sup o}C. (author)

  3. Optical Characterization of Commercial Lithiated Graphite Battery Electrodes and in Situ Fiber Optic Evanescent Wave Spectroscopy.

    Science.gov (United States)

    Ghannoum, AbdulRahman; Norris, Ryan C; Iyer, Krishna; Zdravkova, Liliana; Yu, Aiping; Nieva, Patricia

    2016-07-27

    Optical characterization of graphite anodes in lithium ion batteries (LIB) is presented here for potential use in estimating their state of charge (SOC). The characterization is based on reflectance spectroscopy of the anode of commercial LIB cells and in situ optical measurements using an embedded optical fiber sensor. The optical characterization of the anode using wavelengths ranging from 500 to 900 nm supports the dominance of graphite over the solid electrolyte interface in governing the anode's reflectance properties. It is demonstrated that lithiated graphite's reflectance has a significant change in the near-infrared band, 750-900 nm, compared with the visible spectrum as a function of SOC. An embedded optical sensor is used to measure the transmittance of graphite anode in the near-infrared band, and the results suggest that a unique inexpensive method may be developed to estimate the SOC of a LIB.

  4. Why LiFePO4 is a safe battery electrode: Coulomb repulsion induced electron-state reshuffling upon lithiation.

    Science.gov (United States)

    Liu, Xiaosong; Wang, Yung Jui; Barbiellini, Bernardo; Hafiz, Hasnain; Basak, Susmita; Liu, Jun; Richardson, Thomas; Shu, Guojiun; Chou, Fangcheng; Weng, Tsu-Chien; Nordlund, Dennis; Sokaras, Dimosthenis; Moritz, Brian; Devereaux, Thomas P; Qiao, Ruimin; Chuang, Yi-De; Bansil, Arun; Hussain, Zahid; Yang, Wanli

    2015-10-21

    LiFePO4 is a battery cathode material with high safety standards due to its unique electronic structure. We performed systematic experimental and theoretical studies based on soft X-ray emission, absorption, and hard X-ray Raman spectroscopy of LixFePO4 nanoparticles and single crystals. The results clearly show a non-rigid electron-state reconfiguration of both the occupied and unoccupied Fe-3d and O-2p states during the (de)lithiation process. We focus on the energy configurations of the occupied states of LiFePO4 and the unoccupied states of FePO4, which are the critical states where electrons are removed and injected during the charge and discharge process, respectively. In LiFePO4, the soft X-ray emission spectroscopy shows that, due to the Coulomb repulsion effect, the occupied Fe-3d states with the minority spin sit close to the Fermi level. In FePO4, the soft X-ray absorption and hard X-ray Raman spectroscopy show that the unoccupied Fe-3d states again sit close to the Fermi level. These critical 3d electron state configurations are consistent with the calculations based on modified Becke and Johnson potentials GGA+U (MBJGGA+U) framework, which improves the overall lineshape prediction compared with the conventionally used GGA+U method. The combined experimental and theoretical studies show that the non-rigid electron state reshuffling guarantees the stability of oxygen during the redox reaction throughout the charge and discharge process of LiFePO4 electrodes, leading to the intrinsic safe performance of the electrodes.

  5. Nitrogen-Doped Porous Carbon Nanosheets from Eco-Friendly Eucalyptus Leaves as High Performance Electrode Materials for Supercapacitors and Lithium Ion Batteries.

    Science.gov (United States)

    Mondal, Anjon Kumar; Kretschmer, Katja; Zhao, Yufei; Liu, Hao; Wang, Chengyin; Sun, Bing; Wang, Guoxiu

    2016-12-31

    Nitrogen-doped porous carbon nanosheets were prepared from eucalyptus tree leaves by simply mixing the leaf powders with KHCO3 and subsequent carbonisation. Porous carbon nanosheets with a high specific surface area of 2133 m(2)  g(-1) were obtained and applied as electrode materials for supercapacitors and lithium ion batteries. For supercapacitor applications, the porous carbon nanosheet electrode exhibited a supercapacitance of 372 F g(-1) at a current density of 500 mA g(-1) in 1 m H2 SO4 aqueous electrolyte and excellent cycling stability over 15 000 cycles. In organic electrolyte, the nanosheet electrode showed a specific capacitance of 71 F g(-1) at a current density of 2 Ag(-1) and stable cycling performance. When applied as the anode material for lithium ion batteries, the as-prepared porous carbon nanosheets also demonstrated a high specific capacity of 819 mA h g(-1) at a current density of 100 mA g(-1) , good rate capability, and stable cycling performance. The outstanding electrochemical performances for both supercapacitors and lithium ion batteries are derived from the large specific surface area, porous nanosheet structure and nitrogen doping effects. The strategy developed in this paper provides a novel route to utilise biomass-derived materials for low-cost energy storage systems.

  6. Bulk-Type All-Solid-State Lithium-Ion Batteries: Remarkable Performances of a Carbon Nanofiber-Supported MgH2 Composite Electrode.

    Science.gov (United States)

    Zeng, Liang; Ichikawa, Takayuki; Kawahito, Koji; Miyaoka, Hiroki; Kojima, Yoshitsugu

    2017-01-25

    Magnesium hydride, MgH2, a recently developed compound for lithium-ion batteries, is considered to be a promising conversion-type negative electrode material due to its high theoretical lithium storage capacity of over 2000 mA h g(-1), suitable working potential, and relatively small volume expansion. Nevertheless, it suffers from unsatisfactory cyclability, poor reversibility, and slow kinetics in conventional nonaqueous electrolyte systems, which greatly limit the practical application of MgH2. In this work, a vapor-grown carbon nanofiber was used to enhance the electrical conductivity of MgH2 using LiBH4 as the solid-state electrolyte. It shows that a reversible capacity of over 1200 mA h g(-1) with an average voltage of 0.5 V (vs Li/Li(+)) can be obtained after 50 cycles at a current density of 1000 mA g(-1). In addition, the capacity of MgH2 retains over 1100 mA h g(-1) at a high current density of 8000 mA g(-1), which indicates the possibility of using MgH2 as a negative electrode material for high power and high capacity lithium-ion batteries in future practical applications. Moreover, the widely studied sulfide-based solid electrolyte was also used to assemble battery cells with MgH2 electrode in the same system, and the electrochemical performance was as good as that using LiBH4 electrolyte.

  7. Nanoscale Polysulfides Reactors Achieved by Chemical Au-S Interaction: Improving the Performance of Li-S Batteries on the Electrode Level.

    Science.gov (United States)

    Fan, Chao-Ying; Xiao, Pin; Li, Huan-Huan; Wang, Hai-Feng; Zhang, Lin-Lin; Sun, Hai-Zhu; Wu, Xing-Long; Xie, Hai-Ming; Zhang, Jing-Ping

    2015-12-23

    In this work, the chemical interaction of cathode and lithium polysulfides (LiPSs), which is a more targeted approach for completely preventing the shuttle of LiPSs in lithium-sulfur (Li-S) batteries, has been established on the electrode level. Through simply posttreating the ordinary sulfur cathode in atmospheric environment just for several minutes, the Au nanoparticles (Au NPs) were well-decorated on/in the surface and pores of the electrode composed of commercial acetylene black (CB) and sulfur powder. The Au NPs can covalently stabilize the sulfur/LiPSs, which is advantageous for restricting the shuttle effect. Moreover, the LiPSs reservoirs of Au NPs with high conductivity can significantly control the deposition of the trapped LiPSs, contributing to the uniform distribution of sulfur species upon charging/discharging. The slight modification of the cathode with <3 wt % Au NPs has favorably prospered the cycle capacity and stability of Li-S batteries. Moreover, this cathode exhibited an excellent anti-self-discharge ability. The slight decoration for the ordinary electrode, which can be easily accessed in the industrial process, provides a facile strategy for improving the performance of commercial carbon-based Li-S batteries toward practical application.

  8. Hydrothermal synthesis of LiMn2O4 onto carbon fiber paper current collector for binder free lithium-ion battery positive electrodes

    Science.gov (United States)

    Waller, Gordon Henry; Lai, Samson Yuxiu; Rainwater, Ben Harris; Liu, Meilin

    2014-04-01

    Concerns over the safety and high cost of lithium ion batteries, especially those containing cobalt-based active materials, limit their use to applications where energy density requirements cannot be met by any other materials. Manganese-spinel based positive electrode materials represent a promising candidate for lithium ion batteries because of their lower cost, lower toxicity, and greater resistance to thermal runaway than cobalt-based active materials. Although LiMn2O4 has a well-known issue of capacity fading, investigations into nanostructured composites composed of surface modified spinel phases have demonstrated outstanding performance, suggesting that LiMn2O4 has potential to be a viable positive electrode for safe, inexpensive, high power, and long lifetime lithium-ion batteries. Here we report a low-temperature hydrothermal process for growth of conformal coatings of highly crystalline LiMn2O4 directly onto a carbon fiber current collector, completely eliminating the process steps and materials associated with the conventional tape casting approach (binders, solvents, and metal foils). The prepared electrodes tested at a rate of 1 C showed an initial discharge capacity of 125 mAh g-1 and an average energy efficiency of 92.4% over 100 cycles.

  9. Three-Dimensional Array of TiN@Pt3Cu Nanowires as an Efficient Porous Electrode for the Lithium-Oxygen Battery.

    Science.gov (United States)

    Luo, Wen-Bin; Pham, Thien Viet; Guo, Hai-Peng; Liu, Hua-Kun; Dou, Shi-Xue

    2017-02-28

    The nonaqueous lithium-oxygen battery is a promising candidate as a next-generation energy storage system because of its potentially high energy density (up to 2-3 kW kg(-1)), exceeding that of any other existing energy storage system for storing sustainable and clean energy to reduce greenhouse gas emissions and the consumption of nonrenewable fossil fuels. To achieve high round-trip efficiency and satisfactory cycling stability, the air electrode structure and the electrocatalysts play important roles. Here, a 3D array composed of one-dimensional TiN@Pt3Cu nanowires was synthesized and employed as a whole porous air electrode in a lithium-oxygen battery. The TiN nanowire was primarily used as an air electrode frame and catalyst support to provide a high electronic conductivity network because of the high-orientation one-dimensional crystalline structure. Meanwhile, deposited icosahedral Pt3Cu nanocrystals exhibit highly efficient catalytic activity owing to the abundant {111} active lattice facets and multiple twin boundaries. This porous air electrode comprises a one-dimensional TiN@Pt3Cu nanowire array that demonstrates excellent energy conversion efficiency and rate performance in full discharge and charge modes. The discharge capacity is up to 4600 mAh g(-1) along with an 84% conversion efficiency at a current density of 0.2 mA cm(-2), and when the current density increased to 0.8 mA cm(-2), the discharge capacity is still greater than 3500 mAh g(-1) together with a nearly 70% efficiency. This designed array is a promising bifunctional porous air electrode for lithium-oxygen batteries, forming a continuous conductive and high catalytic activity network to facilitate rapid gas and electrolyte diffusion and catalytic reaction throughout the whole energy conversion process.

  10. Solid-state sodium batteries using polymer electrolytes and sodium intercalation electrode materials

    Energy Technology Data Exchange (ETDEWEB)

    Ma, Y. [Univ. of California, Berkeley, CA (United States). Dept. of Materials Science and Mineral Engineering]|[Lawrence Berkeley National Lab., CA (United States). Materials Sciences Div.

    1996-08-01

    Solid-state sodium cells using polymer electrolytes (polyethylene oxide mixed with sodium trifluoromethanesulfonate: PEO{sub n}NaCF{sub 3}SO{sub 3}) and sodium cobalt oxide positive electrodes are characterized in terms of discharge and charge characteristics, rate capability, cycle life, and energy and power densities. The P2 phase Na{sub x}CoO{sub 2} can reversibly intercalate sodium in the range of x = 0.3 to 0.9, giving a theoretical specific energy of 440 Wh/kg and energy density of 1,600 Wh/l. Over one hundred cycles to 60% depth of discharge have been obtained at 0.5 mA/cm{sup 2}. Experiments show that the electrolyte/Na interface is stable and is not the limiting factor to cell cycle life. Na{sub 0.7}CoO{sub 2} composite electrodes containing various amounts of carbon black additive are investigated. The transport properties of polymer electrolytes are the critical factors for performance. These properties (the ionic conductivity, salt diffusion coefficient, and ion transference number) are measured for the PEO{sub n}NaCF{sub 3}SO{sub 3} system over a wide range of concentrations at 85 C. All the three transport properties are very salt-concentration dependent. The ionic conductivity exhibits a maximum at about n = 20. The transference number, diffusion coefficient, and thermodynamic factor all vary with salt concentration in a similar fashion, decreasing as the concentration increases, except for a local maximum. These results verify that polymer electrolytes cannot be treated as ideal solutions. The measured transport-property values are used to analyze and optimize the electrolytes by computer simulation and also cell testing. Salt precipitation is believed to be the rate limiting process for cells using highly concentrated solutions, as a result of lower values of these properties, while salt depletion is the limiting factor when a dilute solution is used.

  11. High capacity hydrogen storage alloy negative electrodes for use in nickel–metal hydride batteries

    Energy Technology Data Exchange (ETDEWEB)

    Inoue, Hiroshi, E-mail: inoue-h@chem.osakafu-u.ac.jp; Kotani, Norihiro; Chiku, Masanobu; Higuchi, Eiji

    2015-10-05

    Highlights: • Rare earth-free TiV{sub 2.1−x}Cr{sub x}Ni{sub 0.3} (x = 0.4–1.0) alloys were prepared by arc-melting. • All alloys were composed of two phases, bcc phase and TiNi-based phase. • The higher Cr content, the lower discharge capacity, the higher cycle durability. • The lower charge-transfer resistance led to the higher HRD. • The TiV{sub 1.6}Cr{sub 0.5}Ni{sub 0.3} alloy electrode had the highest HRD. - Abstract: Rare earth-free V-based TiV{sub 2.1−x}Cr{sub x}Ni{sub 0.3} (x = 0.4–1.0) alloys were prepared by arc-melting. All alloys were composed of two phases, the primary phase in which the V and Cr constituents were mainly distributed and the secondary phase in which the Ti and Ni constituents were mainly distributed. When the Cr content was increased, the maximum discharge capacity was decreased, but charge–discharge cycle durability was improved. The lower the charge-transfer resistance and the higher the specific discharge current at which the positive shift of potential at degree of discharge of 50% stagnates, the higher the HRD. In the present study, the TiV{sub 1.6}Cr{sub 0.5}Ni{sub 0.3} alloy electrode had the highest HRD.

  12. Layered double hydroxides as electrode materials for Ni based batteries and as novel inorganic/organic hybrid materials

    Energy Technology Data Exchange (ETDEWEB)

    Caravaggio, G.

    2002-07-01

    This study examined the electrochemical properties of layered double hydroxides (LDH) in half-cells to determine if they can be used in nickel-cadmium (Ni-Cd) and nickel-metal hydride (NiMH) batteries. The LDHs were prepared by coprecipitation and were characterized by X-ray diffraction analysis. The nickel-aluminium LDHs were found to be the most stable during potassium hydroxide electrolyte discharge because the aluminium acted in a two fold manner. The high charge to radius ratio increased the electrostatic interaction between the anions and the metal layers. The acidity of the hydroxyl groups was due to the high exchange of electrons. The powders had lower discharge capacity compared to commercial electrode materials because of their low density. The nickel-vanadium LDHs exchanged only up to 1.2 electrons and were stable only up to a maximum of 14 days in electrolytic solutions of the cells. Zinc-aluminium LDHs were also synthesized and intercalated with phenyl phosphonic acid or 1,4-phenylene bis phosphonic acid to create microporous materials. X-ray diffraction, infra-red spectroscopy and nuclear magnetic resonance was used to characterize the compounds and determine crystallographic spacing. Grafting of both phosphonates to the metal layers had occurred and both materials showed little or no microporosity.

  13. Electrochemical properties of LaMO3 (M=Co or Fe) as the negative electrode in a hydrogen battery

    Science.gov (United States)

    Lim, D.-K.; Im, H.-N.; Kim, J.; Song, S.-J.

    2013-01-01

    Undoped orthorthombic LaFeO3 and monoclinic LaCoO3 oxides were selected as an anode material for Ni-H battery due to their high electron conductivity by multivalent transition status of B-site cation. Both groups of oxides were prepared by a conventional solid-state reaction method, and their electrochemical charge/discharge properties were investigated. The electrochemical kinetic properties, exchange current density, and proton diffusivity were also extracted using linear polarization measurement and the potential-step method. X-ray photoelectron spectroscopy (XPS) analysis was used to measure the oxidation state of the transition metal in the specimens. A non-linear least-square fitting deconvoluted the peaks, suggesting that the valence state of Fe and Co in the sample was mainly +3. The hydrogen diffusion rate was also estimated using the potential-step method, giving 5.42×10-16 and 5.72×10-16 cm2 s-1 for LaCoO3 and LaFeO3, respectively which are an order of magnitude larger than that of Sr doped LaFeO3 oxide electrodes.

  14. Li2CuVO4: A high capacity positive electrode material for Li-ion batteries

    Science.gov (United States)

    Ben Yahia, Hamdi; Shikano, Masahiro; Yamaguchi, Yoichi

    2016-07-01

    The new compound Li2CuVO4 was synthesized by a solid state reaction route, and its crystal structure was determined from single crystal X-ray diffraction data. Li2CuVO4 was characterized by galvanometric cycling, cycle voltammetry, and electrochemical impedance spectroscopy. The structure of Li2CuVO4 is isotypic to Pmn21-Li3VO4. It can be described as a disordered wurtzite structure with rows of Li1/Cu1 atoms alternating with rows of (Li2/Cu2)-V-(Li2/Cu2) atoms along [100]. All cations are tetrahedrally coordinated. The lithium and copper atoms are statistically disordered over two crystallographic sites. The electrochemical cycling between 2.0 and 4.7 V indicates that almost two lithium atoms could be extracted and re-intercalated. This delivers a maximum discharge capacity of 257 mA h g-1 at a C/50 rate (theoretical capacity = 139 mA h g-1 for one lithium). Li2CuVO4 shows also high rate capability with a capacity of 175 mA h g-1 at 1C rate. This demonstrates that Cu-based compounds can be very interesting as electrodes for Li-ion batteries if Cu-dissolution is avoided.

  15. Nano-sized structured layered positive electrode materials to enable high energy density and high rate capability lithium batteries

    Science.gov (United States)

    Deng, Haixia; Belharouak, Ilias; Amine, Khalil

    2012-10-02

    Nano-sized structured dense and spherical layered positive active materials provide high energy density and high rate capability electrodes in lithium-ion batteries. Such materials are spherical second particles made from agglomerated primary particles that are Li.sub.1+.alpha.(Ni.sub.xCo.sub.yMn.sub.z).sub.1-tM.sub.tO.sub.2-dR.sub.d- , where M is selected from can be Al, Mg, Fe, Cu, Zn, Cr, Ag, Ca, Na, K, In, Ga, Ge, V, Mo, Nb, Si, Ti, Zr, or a mixture of any two or more thereof, R is selected from F, Cl, Br, I, H, S, N, or a mixture of any two or more thereof, and 0.ltoreq..alpha..ltoreq.0.50; 0

  16. EELS spectroscopy of iron fluorides and FeFx/C nanocomposite electrodes used in Li-ion batteries.

    Science.gov (United States)

    Cosandey, Frederic; Al-Sharab, Jafar F; Badway, Fadwa; Amatucci, Glenn G; Stadelmann, Pierre

    2007-04-01

    A new type of positive electrode for Li-ion batteries has been developed recently based on FeF3/C and FeF2/C nanocomposites. The microstructural and redox evolution during discharge and recharge processes was followed by electron energy loss spectroscopy (EELS) to determine the valence state of Fe by measuring the Fe L3 line energy shift and from Fe L3/L2 line intensity ratios. In addition, transition metal fluorides were found to be electron beam sensitive, and the effect of beam exposure on EELS spectra was also investigated. The EELS results indicate that for both FeF3/C and FeF2/C nanocomposite systems, a complete reduction of iron to FeO is observed upon discharge to 1.5 V with the formation of a finer FeO/LiF subnanocomposite ( approximately 7 nm). Upon complete recharging to 4.5 V, EELS data reveal a reoxidation process to a Fe2+ state with the formation of a carbon metal fluoride nanocomposite related to the FeF2 structure.

  17. The Effect of Insertion Species on Nanostructured Open Framework Hexacyanoferrate Battery Electrodes

    KAUST Repository

    Wessells, Colin D.

    2012-01-01

    Recent battery research has focused on the high power and energy density needed for portable electronics and vehicles, but the requirements for grid-scale energy storage are different, with emphasis on low cost, long cycle life, and safety. Open framework materials with the Prussian Blue crystal structure offer the high power capability, ultra-long cycle life, and scalable, low cost synthesis and operation that are necessary for storage systems to integrate transient energy sources, such as wind and solar, with the electrical grid. We have demonstrated that two open framework materials, copper hexacyanoferrate and nickel hexacyanoferrate, can reversibly intercalate lithium, sodium, potassium, and ammonium ions at high rates. These materials can achieve capacities of up to 60 mAhg. The porous, nanoparticulate morphology of these materials, synthesized by the use of simple and inexpensive methods, results in remarkable rate capabilities: e.g. copper hexacyanoferrate retains 84 of its maximum capacity during potassium cycling at a very high (41.7C) rate, while nickel hexacyanoferrate retains 66 of its maximum capacity while cycling either sodium or potassium at this same rate. These materials show excellent stability during the cycling of sodium and potassium, with minimal capacity loss after 500 cycles. © 2011 The Electrochemical Society.

  18. Biomineralized Sn-based multiphasic nanostructures for Li-ion battery electrodes.

    Science.gov (United States)

    Lim, Ah-Hyeon; Shim, Hyun-Woo; Seo, Seung-Deok; Lee, Gwang-Hee; Park, Kyung-Soo; Kim, Dong-Wan

    2012-08-07

    A method for preparing multiphasic hollow rods consisting of nanoscale Sn-based materials through a thermochemical reduction process involving bacteria and Sn oxides is reported. This facile process involves the bacteria-mediated synthesis of SnO(2) nanoparticles that form on bacterial surfaces used as templates at room temperature. The subsequent template removal proceeds via a reduction of the heat-treated SnO(2) nanoparticles at 400 °C under reduction atmosphere, leaving free-standing hollow nanocomposite rods. These unique hollow nanocomposite rods have multiple components, including amorphous carbon, metal oxides (SnO(2) and SnO), and metallic Sn, and retain the original rod shapes. The systematic phase and morphological evolutions of the bacteria@SnO(2) composite rods are investigated by performing controlled thermochemical reduction at various temperatures. In addition, the application of multiphasic hollow nanocomposite rods as anode materials for rechargeable Li-ion batteries is evaluated. These materials exhibit excellent electrochemical performance, with capacities of about 505 and 350 mA h g(-1) at current densities of 157 and 392 mA g(-1), respectively.

  19. Effect of mesocelluar carbon foam electrode material on performance of vanadium redox flow battery

    Science.gov (United States)

    Jeong, Sanghyun; An, Sunhyung; Jeong, Jooyoung; Lee, Jinwoo; Kwon, Yongchai

    2015-03-01

    Languid reaction rate of VO2+/VO2+ redox couple is a problem to solve for improving performance of vanadium redox flow battery (VRFB). To facilitate the slow reaction materials including large pore sized mesocellular carbon foam (MSU-F-C and Pt/MSU-F-C) are used as new catalyst. Their catalytic activity and reaction reversibility are estimated and compared with other catalysts, while cycle tests of charge-discharge and polarization curve tests are implemented to evaluate energy efficiency (EE) and maximum power density (MPD). Their crystal structure, specific surface area and catalyst morphology are measured by XRD, BET and TEM. The new catalysts indicate high peak current ratio, small peak potential difference and high electron transfer rate constant, proving that their catalytic activity and reaction reversibility are superior. Regarding the charge-discharge and polarization curve tests, the VRFB single cells including new catalysts show high EE as well as low overpotential and internal resistance and high MPD. Such excellent results are due to mostly unique characteristics of MSU-F-C having large interconnected mesopores, high surface area and large contents of hydroxyl groups that serve as active sites for VO2+/VO2+ redox reaction and platinums (Pts) supporting the MSU-F-C. Indeed, employment of the catalysts including MSU-F-C leads to enhancement in performance of VRFB by facilitating the slow VO2+/VO2+ redox reaction.

  20. Carbon- and Binder-Free NiCo2O4 Nanoneedle Array Electrode for Sodium-Ion Batteries: Electrochemical Performance and Insight into Sodium Storage Reaction

    Science.gov (United States)

    Lee, Jong-Won; Shin, Hyun-Sup; Lee, Chan-Woo; Jung, Kyu-Nam

    2016-02-01

    Sodium (Na)-ion batteries (NIBs) have attracted significant interest as an alternative chemistry to lithium (Li)-ion batteries for large-scale stationary energy storage systems. Discovering high-performance anode materials is a great challenge for the commercial success of NIB technology. Transition metal oxides with tailored nanoarchitectures have been considered as promising anodes for NIBs due to their high capacity. Here, we demonstrate the fabrication of a nanostructured oxide-only electrode, i.e., carbon- and binder-free NiCo2O4 nanoneedle array (NCO-NNA), and its feasibility as an anode for NIBs. Furthermore, we provide an in-depth experimental study of the Na storage reaction (sodiation and desodiation) in NCO-NNA. The NCO-NNA electrode is fabricated on a conducting substrate by a hydrothermal method with subsequent heat treatment. When tested in an electrochemical Na half-cell, the NCO-NNA electrode exhibits excellent Na storage capability: a charge capacity as high as 400 mAh g-1 is achieved at a current density of 50 mA g-1. It also shows a greatly improved cycle life (~215 mAh g-1 after 50 cycles) in comparison to a conventional powder-type electrode (~30 mAh g-1). However, the Na storage performance is still inferior to that of Li, which is mainly due to sluggish kinetics of sodiation-desodiation accompanied by severe volume change.

  1. Bipolar lead acid batteries with ceramic partitioning walls. Forming and characterization of negative electrodes; Bipolaera blybatterier med keramiska mellanvaeggar. Tillverkning och karaktaerisering av negativa elektroder

    Energy Technology Data Exchange (ETDEWEB)

    Nilsson, Ove; Haraldsen, Britta [Chalmers Univ. of Technology, Goeteborg (Sweden). Environmental Inorganic Chemistry

    2001-01-01

    Bipolar electrodes are built with positive and negative paste on each side of a partitioning wall (PW). The PW must be dimensional stable and shall not allow electrolyte to flow through. The process of lead infiltration in porous ceramic plates is studied in this report in combination with different methods of forming pos. and neg. halves. Plante formed negative paste can not withstand a high pressure - relief details must be included in the design. The expanders in NAM are necessary to maintain the capacity. Positive Plante formed electrodes are not proper formed due to a too high current density. Furthermore, they are very brittle. The usefulness of paste plates has been shown and the future work will be directed towards such bipolar electrodes to be included in prototype batteries.

  2. New hydrogen titanium phosphate sulfate electrodes for Li-ion and Na-ion batteries

    Science.gov (United States)

    Zhao, Ran; Mieritz, Daniel; Seo, Dong-Kyun; Chan, Candace K.

    2017-03-01

    NASICON-type materials with general formula AxM2(PO4)3 (A = Li or Na, M = Ti, V, and Fe) are promising candidates for Li- and Na-ion batteries due to their open three-dimensional framework structure. Here we report the electrochemical properties of hydrogen titanium phosphate sulfate, H0.4Ti2(PO4)2.4(SO4)0.6 (HTPS), a new mixed polyanion material with NASICON structure. Micron-sized HTPS aggregates with crystallite grain size of ca. 23 nm are synthesized using a sol-gel synthesis in an acidic medium. The properties of the as-synthesized HTPS, ball-milled HTPS, and samples prepared as carbon composites using an in-situ glucose decomposition reaction are investigated. A capacity of 148 mAh g-1 corresponding to insertion of 2 Li+ per formula unit is observed in the ball-milled HTPS over the potential window of 1.5-3.4 V vs. Li/Li+. Lithiation at ca. 2.8 and 2.5 V is determined to occur through filling of the M1 and M2 sites, respectively. Powder X-ray diffraction (PXRD), scanning electron microscopy (SEM) and X-ray photoelectron spectroscopy (XPS) are used characterize the HTPS before and after cycling. Evaluation of the HTPS in a Na-ion cell is also performed. A discharge capacity of 93 mAh g-1 with sodiation at ca. 2.9 and 2.2 V vs. Na/Na+ is observed.

  3. Development of non-flammable lithium secondary battery with room-temperature ionic liquid electrolyte: Performance of electroplated Al film negative electrode

    Energy Technology Data Exchange (ETDEWEB)

    Ui, Koichi; Yamamoto, Keigo; Ishikawa, Kohei; Minami, Takuto; Takeuchi, Ken; Itagaki, Masayuki; Watanabe, Kunihiro; Koura, Nobuyuki [Faculty of Science and Technology, Tokyo University of Science, Noda, Chiba 278-8510 (Japan)

    2008-08-15

    The negative electrode performance of the electroplated Al film electrode in the LiCl saturated AlCl{sub 3}-1-ethyl-3-methylimizadolium chloride (EMIC) + SOCl{sub 2} melt as the electrolyte for use in non-flammable lithium secondary batteries was evaluated. In the cyclic voltammogram of the electroplated Al film electrode in the melt, the oxidation and reduction waves corresponding to the electrochemical insertion/extraction reactions of the Li{sup +} ion were observed at 0-0.80 V vs. Li{sup +}/Li, which suggested that the electroplated Al film electrode operated well in the electrolyte. The almost flat potential profiles at about 0.40 V vs. Li{sup +}/Li on discharging were shown. The discharge capacity and charge-discharge efficiency was 236 mAh g{sup -1} and 79.2% for the 1st cycle and it maintained 232 mAh g{sup -1} and 77.9% after the 10th cycle. In addition, the initial charge-discharge efficiencies of the electroplated Al film electrode were higher than that of carbon electrodes. The main cathodic polarization reaction was the insertion of Li{sup +} ions, and side reactions hardly occurred due to the decomposition reaction of the melt because the Li content corresponding to the electricity was almost totally inserted into the film after charging. (author)

  4. Li-rich Li-Si alloy as a lithium-containing negative electrode material towards high energy lithium-ion batteries.

    Science.gov (United States)

    Iwamura, Shinichiroh; Nishihara, Hirotomo; Ono, Yoshitaka; Morito, Haruhiko; Yamane, Hisanori; Nara, Hiroki; Osaka, Tetsuya; Kyotani, Takashi

    2015-01-28

    Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell.

  5. Original implementation of Electrochemical Impedance Spectroscopy (EIS) in symmetric cells: Evaluation of post-mortem protocols applied to characterize electrode materials for Li-ion batteries

    Science.gov (United States)

    Gordon, Isabel Jiménez; Genies, Sylvie; Si Larbi, Gregory; Boulineau, Adrien; Daniel, Lise; Alias, Mélanie

    2016-03-01

    Understanding ageing mechanisms of Li-ion batteries is essential for further optimizations. To determine performance loss causes, post-mortem analyses are commonly applied. For each type of post-mortem test, different sample preparation protocols are adopted. However, reports on the reliability of these protocols are rare. Herein, Li-ion pouch cells with LiNi1/3Mn1/3Co1/3O2 - polyvinylidene fluoride positive electrode, graphite-carboxymethyl cellulose-styrene rubber negative electrode and LiPF6 - carbonate solvents mixture electrolyte, are opened and electrodes are recovered following a specified protocol. Negative and positive symmetric cells are assembled and their impedances are recorded. A signal analysis is applied to reconstruct the Li-ion pouch cell impedance from the symmetric cells, then comparison against the pouch cell true impedance allows the evaluation of the sample preparation protocols. The results are endorsed by Transmission Electronic Microscopy (TEM) and Gas Chromatography - Mass Spectrometry (GC-MS) analyses. Carbonate solvents used to remove the salt impacts slightly the surface properties of both electrodes. Drying electrodes under vacuum at 25 °C produces an impedance increase, particularly very marked for the positive electrode. Drying at 50 °C under vacuum or/and exposition to the anhydrous room atmosphere is very detrimental.

  6. Sn-0.4BPO 4 composite as a promising negative electrode for rechargeable lithium batteries

    Science.gov (United States)

    Aboulaich, Abdelmaula; Womes, Manfred; Olivier-Fourcade, Josette; Willmann, Patrick; Jumas, Jean-Claude

    2010-01-01

    The structural and textural properties of a Sn-0.4BPO 4 composite material synthesized by ex situ dispersion of β-Sn in a BPO 4 matrix were investigated by using several complementary techniques to study the global order (XRD, TGA-DSC, SEM-XEDS) and the local order (FT-IR, 119Sn Mössbauer spectroscopy and X-ray absorption spectroscopy). The results reveal that the composite material consists of three main components: an electrochemically active species "Sn", an inactive matrix "BPO 4", and an amorphous Sn(II) borophosphate which acts as a link between the two former and which improves the cohesion of the composite. The electrochemical performances of the composite material were tested in Swagelok-type cells with metallic Li as counter-electrode. It shows a high reversible capacity of about 500 mAh g -1 at a C/20 rate, and a very good stability under cycling even at very fast rates of C or C/1.3.

  7. Carbothermal synthesis of Sn-based composites as negative electrode for lithium-ion batteries

    Science.gov (United States)

    Mouyane, M.; Ruiz, J.-M.; Artus, M.; Cassaignon, S.; Jolivet, J.-P.; Caillon, G.; Jordy, C.; Driesen, K.; Scoyer, J.; Stievano, L.; Olivier-Fourcade, J.; Jumas, J.-C.

    The composite [Sn-BPO 4/ xC] to be used as negative electrode material for the storage of electrochemical energy was obtained by dispersing electroactive tin species onto a BPO 4 buffer matrix by carbothermal reduction of a mixture of SnO 2 and nanosized BPO 4. This composite material was thoroughly characterized by X-ray diffraction, Scanning Electron Microscopy, 119Sn Mössbauer spectroscopy and Raman spectroscopy. The electrochemical tests of this new material highlight its very interesting electrochemical properties, i.e., a discharge capacity of 850 mAh g -1 for the first cycle and reversible capacity around 585 mAh g -1 at C/5 rate. These electrochemical performances are attributed to the very high dispersion and stabilisation of tin metal particles onto the BPO 4 matrix. The irreversible capacity observed for the first charge/discharge cycle is due the reduction of interfacial Sn II species and to the passivation of the anode surface by liquid electrolyte decomposition (formation of the SEI layer).

  8. In situ and operando atomic force microscopy of high-capacity nano-silicon based electrodes for lithium-ion batteries

    Science.gov (United States)

    Breitung, Ben; Baumann, Peter; Sommer, Heino; Janek, Jürgen; Brezesinski, Torsten

    2016-07-01

    Silicon is a promising next-generation anode material for high-energy-density lithium-ion batteries. While the alloying of nano- and micron size silicon with lithium is relatively well understood, the knowledge of mechanical degradation and structural rearrangements in practical silicon-based electrodes during operation is limited. Here, we demonstrate, for the first time, in situ and operando atomic force microscopy (AFM) of nano-silicon anodes containing polymer binder and carbon black additive. With the help of this technique, the surface topography is analyzed while electrochemical reactions are occurring. In particular, changes in particle size as well as electrode structure and height are visualized with high resolution. Furthermore, the formation and evolution of the solid-electrolyte interphase (SEI) can be followed and its thickness determined by phase imaging and nano-indentation, respectively. Major changes occur in the first lithiation cycle at potentials below 0.6 V with respect to Li/Li+ due to increased SEI formation - which is a dynamic process - and alloying reactions. Overall, these results provide insight into the function of silicon-based composite electrodes and further show that AFM is a powerful technique that can be applied to important battery materials, without restriction to thin film geometries.Silicon is a promising next-generation anode material for high-energy-density lithium-ion batteries. While the alloying of nano- and micron size silicon with lithium is relatively well understood, the knowledge of mechanical degradation and structural rearrangements in practical silicon-based electrodes during operation is limited. Here, we demonstrate, for the first time, in situ and operando atomic force microscopy (AFM) of nano-silicon anodes containing polymer binder and carbon black additive. With the help of this technique, the surface topography is analyzed while electrochemical reactions are occurring. In particular, changes in particle

  9. Novel lead-graphene and lead-graphite metallic composite materials for possible applications as positive electrode grid in lead-acid battery

    Science.gov (United States)

    Yolshina, L. A.; Yolshina, V. A.; Yolshin, A. N.; Plaksin, S. V.

    2015-03-01

    Novel lead-graphene and lead-graphite metallic composites which melt at temperature of the melting point of lead were investigated as possible positive current collectors for lead acid batteries in sulfuric acid solution. Scanning electron microscopy, Raman spectroscopy, difference scanning calorimetry, cyclic voltammetry and prolonged corrosion tests were employed to characterize the effect of the newly proposed lead-carbon metallic composites on the structure and electrochemical properties of positive grid material. Both lead-graphene and lead-graphite metallic composite materials show the similar electrochemical characteristics to metallic lead in the voltage range where the positive electrodes of lead acid batteries operate. It has been shown that carbon both as graphene and graphite does not participate in the electrochemical process but improve corrosion and electrochemical characteristics of both metallic composite materials. No products of interaction of lead with sulfuric acid were formed on the surface of graphene and graphite so as it was not found additional peaks of carbon discharge on voltammograms which could be attributed to the carbon. Graphene inclusions in lead prevent formation of leady oxide nanocrystals which deteriorate discharge characteristics of positive electrode of LAB. Both lead-graphene alloy and lead-graphite metallic composite proved excellent electrochemical and corrosion behavior and can be used as positive grids in lead acid batteries of new generation.

  10. Carbon electrode with NiO and RuO2 nanoparticles improves the cycling life of non-aqueous lithium-oxygen batteries

    Science.gov (United States)

    Tan, P.; Shyy, W.; Wu, M. C.; Huang, Y. Y.; Zhao, T. S.

    2016-09-01

    Carbon has been regarded as one of the most attractive cathode materials for non-aqueous lithium-oxygen batteries due to its excellent conductivity, high specific area, large porosity, and low cost. However, a key disadvantage of carbon electrodes lies in the fact that carbon may react with Li2O2 and electrolyte to form irreversible side products (e.g. Li2CO3) at the active surfaces, leading to a high charge voltage and a short cycling life. In this work, we address this issue by decorating NiO and RuO2 nanoparticles onto carbon surfaces. It is demonstrated that the NiO-RuO2 nanoparticle-decorated carbon electrode not only catalyzes both the oxygen reduction and evolution reactions, but also promotes the decomposition of side products. As a result, the battery fitted with the novel carbon cathode delivers a capacity of 3653 mAh g-1 at a current density of 400 mA g-1, with a charge plateau of 4.01 V. This performance is 440 mV lower than that of the battery fitted with a pristine carbon cathode. The present cathode is also able to operate for 50 cycles without capacity decay at a fixed capacity of 1000 mAh g-1, which is more than twice the cycle number of that of the pristine carbon cathode.

  11. High-resolution chemical analysis on cycled LiFePO4 battery electrodes using energy-filtered transmission electron microscopy

    Science.gov (United States)

    Sugar, Joshua D.; El Gabaly, Farid; Chueh, William C.; Fenton, Kyle R.; Tyliszczak, Tolek; Kotula, Paul G.; Bartelt, Norman C.

    2014-01-01

    We demonstrate an ex situ method for analyzing the chemistry of battery electrode particles after electrochemical cycling using the transmission electron microscope (TEM). The arrangement of particles during our analysis is the same as when the particles are being cycled. We start by sectioning LiFePO4 battery electrodes using an ultramicrotome. We then show that mapping of the Fe2+ and Fe3+ oxidation state using energy-filtered TEM (EFTEM) and multivariate statistical analysis techniques can be used to determine the spatial distribution of Li in the particles. This approach is validated by comparison with scanning transmission X-ray microscopy (STXM) analysis of the same samples [Chueh et al. Nanoletters, 13 (3) (2013) 866-72]. EFTEM uses a parallel electron beam and reduces the electron-beam dose (and potential beam-induced damage) to the sample when compared to alternate techniques that use a focused probe (e.g. STEM-EELS). Our analysis confirms that under the charging conditions of the analyzed battery, mixed phase particles are rare and thus Li intercalation is limited by the nucleation of new phases.

  12. Electrochemical and thermodynamic studies of the electrode materials for lithium ion batteries

    Science.gov (United States)

    Bang, Hyun Joo

    profiles observed during the charge and discharge processes are related to the Li insertion/extraction reaction in the spinel host structure for both materials. The reversible heat generation due to the lithium insertion/extraction reaction in the host electrode is estimated on the basis of the cell entropy change. The heat generation calculated from DeltaS and the open circuit potential results is consistent with the heat profile (exothermic/endothermic) generated during the charge/discharge process and with the magnitude of the heat generation from the experimental results obtained from the IMC at a slow charge/discharge rate. The irreversible heat generation dependence on the current rate is discussed at different discharge rates.

  13. Multi-layer electrode with nano-Li4Ti5O12 aggregates sandwiched between carbon nanotube and graphene networks for high power Li-ion batteries.

    Science.gov (United States)

    Choi, Jin-Hoon; Ryu, Won-Hee; Park, Kyusung; Jo, Jeong-Dai; Jo, Sung-Moo; Lim, Dae-Soon; Kim, Il-Doo

    2014-12-05

    Self-aggregated Li4Ti5O12 particles sandwiched between graphene nanosheets (GNSs) and single-walled carbon nanotubes (SWCNTs) network are reported as new hybrid electrodes for high power Li-ion batteries. The multi-layer electrodes are fabricated by sequential process comprising air-spray coating of GNSs layer and the following electrostatic spray (E-spray) coating of well-dispersed colloidal Li4Ti5O12 nanoparticles, and subsequent air-spray coating of SWCNTs layer once again. In multi-stacked electrodes of GNSs/nanoporous Li4Ti5O12 aggregates/SWCNTs networks, GNSs and SWCNTs serve as conducting bridges, effectively interweaving the nanoporous Li4Ti5O12 aggregates, and help achieve superior rate capability as well as improved mechanical stability of the composite electrode by holding Li4Ti5O12 tightly without a binder. The multi-stacked electrodes deliver a specific capacity that maintains an impressively high capacity of 100 mA h g(-1) at a high rate of 100C even after 1000 cycles.

  14. In situ SEM observation of the Si negative electrode reaction in an ionic-liquid-based lithium-ion secondary battery.

    Science.gov (United States)

    Tsuda, Tetsuya; Kanetsuku, Tsukasa; Sano, Teruki; Oshima, Yoshifumi; Ui, Koichi; Yamagata, Masaki; Ishikawa, Masashi; Kuwabata, Susumu

    2015-06-01

    By exploiting characteristics such as negligible vapour pressure and ion-conductive nature of an ionic liquid (IL), we established an in situ scanning electron microscope (SEM) method to observe the electrode reaction in the IL-based Li-ion secondary battery (LIB). When 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)amide ([C2mim][FSA]) with lithium bis(trifluoromethanesulfonyl)amide (Li[TFSA]) was used as the electrolyte, the Si negative electrode exhibited a clear morphology change during the charge process, without any solid electrolyte interphase (SEI) layer formation, while in the discharge process, the appearance was slightly changed, suggesting that a morphology change is irreversible in the charge-discharge process. On the other hand, the use of 1-ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)amide ([C2mim][TFSA]) with Li[TFSA] did not induce a change in the Si negative electrode. It is interesting to note this distinct contrast, which could be attributed to SEI layer formation from the electrochemical breakdown of [C2mim](+) at the Si negative electrode|separator interface in the [C2mim][TFSA]-based LIB. This in situ SEM observation technique could reveal the effect of the IL species electron-microscopically on the Si negative electrode reaction.

  15. Multi-layer electrode with nano-Li4Ti5O12 aggregates sandwiched between carbon nanotube and graphene networks for high power Li-ion batteries

    Science.gov (United States)

    Choi, Jin-Hoon; Ryu, Won-Hee; Park, Kyusung; Jo, Jeong-Dai; Jo, Sung-Moo; Lim, Dae-Soon; Kim, Il-Doo

    2014-12-01

    Self-aggregated Li4Ti5O12 particles sandwiched between graphene nanosheets (GNSs) and single-walled carbon nanotubes (SWCNTs) network are reported as new hybrid electrodes for high power Li-ion batteries. The multi-layer electrodes are fabricated by sequential process comprising air-spray coating of GNSs layer and the following electrostatic spray (E-spray) coating of well-dispersed colloidal Li4Ti5O12 nanoparticles, and subsequent air-spray coating of SWCNTs layer once again. In multi-stacked electrodes of GNSs/nanoporous Li4Ti5O12 aggregates/SWCNTs networks, GNSs and SWCNTs serve as conducting bridges, effectively interweaving the nanoporous Li4Ti5O12 aggregates, and help achieve superior rate capability as well as improved mechanical stability of the composite electrode by holding Li4Ti5O12 tightly without a binder. The multi-stacked electrodes deliver a specific capacity that maintains an impressively high capacity of 100 mA h g-1 at a high rate of 100C even after 1000 cycles.

  16. The interaction of consecutive process steps in the manufacturing of lithium-ion battery electrodes with regard to structural and electrochemical properties

    Science.gov (United States)

    Bockholt, Henrike; Indrikova, Maira; Netz, Andreas; Golks, Frederik; Kwade, Arno

    2016-09-01

    The individual steps in the electrode manufacturing process, e.g., conductive additives addition, mixing, and calendering, strongly affect the electrochemical and mechanical properties of the electrodes. LiNi1/3Co1/3Mn1/3O2 (NCM) cathode electrodes with conductive additive variations are fabricated using a reference and an intensive mixing process, and are subsequently calendered to different porosities. It is found that graphite reduces the pore size of NCM electrodes, in contrast to the carbon black that establishes additional nanoscale pores. Electrodes manufactured with reference mixing result in a porous carbon black network with good overall electric pathways, whereas those manufactured with intensive processing result in a dense carbon black network, leading to good short-range contacts, but a lack of long-range contacts. In this case, the addition of graphite as a conductive additive is identified to establish important additional long-range contacts. Due to the structural differences achieved by the compared processing routes, the calendering process can have a positive or negative impact on battery performance.

  17. A Metal-Free, Free-Standing, Macroporous Graphene@g-C₃N₄ Composite Air Electrode for High-Energy Lithium Oxygen Batteries.

    Science.gov (United States)

    Luo, Wen-Bin; Chou, Shu-Lei; Wang, Jia-Zhao; Zhai, Yu-Chun; Liu, Hua-Kun

    2015-06-01

    The nonaqueous lithium oxygen battery is a promising candidate as a next-generation energy storage system because of its potentially high energy density (up to 2-3 kW kg(-1)), exceeding that of any other existing energy storage system for storing sustainable and clean energy to reduce greenhouse gas emissions and the consumption of nonrenewable fossil fuels. To achieve high energy density, long cycling stability, and low cost, the air electrode structure and the electrocatalysts play important roles. Here, a metal-free, free-standing macroporous graphene@graphitic carbon nitride (g-C3N4) composite air cathode is first reported, in which the g-C3N4 nanosheets can act as efficient electrocatalysts, and the macroporous graphene nanosheets can provide space for Li2O2 to deposit and also promote the electron transfer. The electrochemical results on the graphene@g-C3N4 composite air electrode show a 0.48 V lower charging plateau and a 0.13 V higher discharging plateau than those of pure graphene air electrode, with a discharge capacity of nearly 17300 mA h g(-1)(composite) . Excellent cycling performance, with terminal voltage higher than 2.4 V after 105 cycles at 1000 mA h g(-1)(composite) capacity, can also be achieved. Therefore, this hybrid material is a promising candidate for use as a high energy, long-cycle-life, and low-cost cathode material for lithium oxygen batteries.

  18. Review of Electrode Materials for Sodium Ion Batteries%钠离子电池电极材料研究进展

    Institute of Scientific and Technical Information of China (English)

    贾旭平; 陈梅

    2012-01-01

    钠是地球上储量较丰富的元素之一,与锂的化学性能类似,因此也可能适用于锂离子电池体系。钠离子电池相比锂离子电池有诸多优势,如成本低,安全性好,随着研究的深入,钠离子电池将越来越具有成本效益,并有望在未来取代锂离子电池而被广泛应用。介绍了钠离子电池正极材料、负极材料的最新研究进展,分析了该电池未来的研究发展方向。%Sodium is one of the more abundant elements on Earth and exhibits similar chemical properties to Li,indicating that Na chemistry could be applied to a similar battery system.Sodium ion batteries have various kinds of advantages,such as low cost,excellent safety,and etc.,which may take place of lithium ion batteries in the future based on successful development.The development of electrode materials of sodium ion batteries was reviewed,and its future development direction was proposed.

  19. Polyvinyl Alcohol-derived carbon nanofibers/carbon nanotubes/sulfur electrode with honeycomb-like hierarchical porous structure for the stable-capacity lithium/sulfur batteries

    Science.gov (United States)

    Deng, Nanping; Kang, Weimin; Ju, Jingge; Fan, Lanlan; Zhuang, Xupin; Ma, Xiaomin; He, Hongsheng; Zhao, Yixia; Cheng, Bowen

    2017-04-01

    The honeycomb-like hierarchical porous carbon nanofibers (PCNFs)-carbon nanotubes (CNTs)-sulfur(S) composite electrode is successfully desgined and prepared through ball-milling and heating method, in which the PCNFs are carbonized from fibers in the membrane composed of Polyvinyl Alcohol and Polytetrafluoroethylene by electro-blown spinning technology. The prepared PCNFs-CNTs-S composite are regarded as cathode for lithium-sulfur battery. The tailored porous structure and CNTs in the composite facilitate construction of a high electrical conductive pathway and store more S/polysulfides, and the dissoluble loss of intermediate S species in electrolyte can also be restrained because of acidized PVA-based porous carbon nanofibers. Meanwhile, the porous strcucture and CNTs can effectively alleviate volume changes in battery cycling process. Moreover, the presence of LiNO3 in electrolyte helps the electrochemical oxidation of Li2S and LiNO3-derived surface film effectively suppresses the migration of soluble polysulfide to the Li anode surface. Therefore, the obtained PCNFs-CNTs-S cathode exhibits excellent performance in Li-S battery with a high initial discharge capacity as high as 1302.9 mAh g-1, and super stable capacity retention with 809.1 mAh g-1 after 300 cycles at the current density of 837.5 mA g-1 (0.5 C). And the rate capability of PCNFs-CNTs-S electrode is much better than those of CNTs-S and PCNFs-S electrodes.

  20. Graphite-silicon-polyacrylate negative electrodes in ionic liquid electrolyte for safer rechargeable Li-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Yabuuchi, Naoaki; Shimomura, Keiji; Shimbe, Yukako; Ozeki, Tomoaki; Komaba, Shinichi [Department of Applied Chemistry, Tokyo University of Science, 1-3 Kagurazaka, Shinjuku, Tokyo 162-8601 (Japan); Son, Jin-Young; Oji, Hiroshi [Japan Synchrotron Radiation Research Institute/SPring-8, 1-1-1 Kouto, Sayo, Hyogo 679-5198 (Japan); Katayama, Yasushi; Miura, Takashi [Department of Applied Chemistry, Faculty of Science and Technology, Keio University, 3-14-1 Hiyoshi, Kohoku, Kanagawa 223-8522 (Japan)

    2011-10-15

    Graphite/silicon composite electrodes are prepared with PANa polymer as a binder. Morphological characters and electrode performance are compared with those of PVdF. The PANa layer behaves like SEI at the interface with ionic liquid, resulting in the highly reversible electrode performance. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  1. Complete Decomposition of Li 2 CO 3 in Li–O 2 Batteries Using Ir/B 4 C as Noncarbon-Based Oxygen Electrode

    Energy Technology Data Exchange (ETDEWEB)

    Song, Shidong; Xu, Wu; Zheng, Jianming; Luo, Langli; Engelhard, Mark H.; Bowden, Mark E.; Liu, Bin; Wang, Chong-Min; Zhang, Ji-Guang

    2017-02-10

    Incomplete decomposition of Li2CO3 during charge process is a critical barrier for rechargeable Li-O2 batteries. Here we report complete decomposition of Li2CO3 in Li-O2 batteries using ultrafine iridium-decorated boron carbide (Ir/B4C) nanocomposite as oxygen electrode. The systematic investigation on charging the Li2CO3 preloaded Ir/B4C electrode in an ether-based electrolyte demonstrates that Ir/B4C electrode can decompose Li2CO3 with an efficiency close to 100% at below 4.37 V. In contrast, the bare B4C without Ir electrocatalyst can only decompose 4.7% of preloaded Li2CO3. The reaction mechanism of Li2CO3 decomposition in the presence of Ir/B4C electrocatalyst has been further investigated. A Li-O2 battery using Ir/B4C as oxygen electrode material shows highly enhanced cycling stability than that using bare B4C oxygen electrode. These results clearly demonstrate that Ir/B4C is an effecitive oxygen electrode amterial to completely decompose Li2CO3 at relatively low charge voltages and is of significant importance in improving the cycle performanc of aprotic Li-O2 batteries.

  2. Electrochemical properties of lithium air batteries with Pt100-xRux (0 ≤ x ≤ 100) electrocatalysts for air electrodes

    Science.gov (United States)

    Yui, Yuhki; Sakamoto, Shuhei; Nohara, Masaya; Hayashi, Masahiko; Nakamura, Jiro; Komatsu, Takeshi

    2017-02-01

    Electrochemical properties of lithium air secondary battery cells with Pt100-xRux (0 ≤ x ≤ 100) electrocatalysts, prepared by the formic acid reduction method and loaded into air electrodes were examined in 1 mol/l LiTFSA/TEGDME electrolyte solution. Among the cells, the one with the Pt10Ru90 (x = 90)/carbon sample showed the largest discharge capacity of 1014 mAh/g and the lowest average charge voltage of 3.74 V. In addition, the x = 90 sample showed comparatively good cycle stability with discharge capacity of over 800 mAh/g at the 8th cycle. As a result, x = 90 was confirmed to be the optimized composition as the electrocatalyst for the air electrode.

  3. Exploration of Ca0.5Ti2(PO4)3@carbon Nanocomposite as the High-Rate Negative Electrode for Na-Ion Batteries.

    Science.gov (United States)

    Wei, Zhixuan; Meng, Xing; Yao, Ye; Liu, Qiang; Wang, Chunzhong; Wei, Yingjin; Du, Fei; Chen, Gang

    2016-12-28

    Exploring suitable electrode materials with high specific capacity and high-rate capability is a challenging goal for the development of Na-ion batteries. Here, we report a NASICON-structured compound, Ca0.5Ti2(PO4)3, with respect to its synthesis and electrochemical properties. The electrode is found to enable fast Na(+) ion diffusion owing to the rich crystallographic vacancies, affording a reversible capacity of 264 mA h g(-1) between 3.0 and 0.01 V. In particular, the hybrid Ca0.5Ti2(PO4)3@carbon exhibits remarkable rate performance with a discharge capacity of nearly 45 mA h g(-1) at a current density of 20 A g(-1), which is attributed to the pseudocapacitive effect.

  4. Effects of electrode properties and fabricated pressure on Li ion diffusion and diffusion-induced stresses in cylindrical Li-ion batteries

    Science.gov (United States)

    Zhang, Tao; Guo, Zhansheng

    2014-03-01

    The effects of electrode properties and fabricated pressure on Li ion diffusion and diffusion-induced stress in a cylindrical Li-ion battery are studied. It is found that hydrostatic pressure or elastic modulus variation in the active layer have little effect on the distribution of Li ions for a higher diffusivity coefficient, but both can facilitate Li ion diffusion for a lower diffusivity coefficient. The elastic modulus variation has a significant effect on the distribution of stress and hydrostatic pressure can reduce the surface stress for the lower diffusivity coefficient. A higher charging rate causes a more transient response in the stress history, but a linear charging history is observed for slow charging rates. A higher charging rate would not inflict extra damage on the electrode for the higher diffusivity coefficient and the stress history becomes highly transient and charging rate dependent for the lower diffusivity coefficient. The effect of fabricated pressure can be neglected.

  5. Aligned carbon nanotube-silicon sheets: a novel nano-architecture for flexible lithium ion battery electrodes.

    Science.gov (United States)

    Fu, Kun; Yildiz, Ozkan; Bhanushali, Hardik; Wang, Yongxin; Stano, Kelly; Xue, Leigang; Zhang, Xiangwu; Bradford, Philip D

    2013-09-25

    Aligned carbon nanotube sheets provide an engineered scaffold for the deposition of a silicon active material for lithium ion battery anodes. The sheets are low-density, allowing uniform deposition of silicon thin films while the alignment allows unconstrained volumetric expansion of the silicon, facilitating stable cycling performance. The flat sheet morphology is desirable for battery construction.

  6. MXenes: A New Family of Two-Dimensional Materials and its Application as Electrodes for Li-ion Batteries

    Science.gov (United States)

    Abdelmalak, Michael Naguib

    Two-dimensional, 2D, materials, such as graphene, possess a unique morphology compared to their 3D counterparts, from which interesting and novel properties arise. Currently, the number of non-oxide materials that have been exfoliated is limited to two fairly small groups, viz. hexagonal, van der Waals bonded structures (e.g. graphene and BN) and layered transition metal chalcogenides. The MAX phases are a well established family of layered ternary transition metal carbides and/or nitrides, with a composition of Mn +1AXn, where M is an early transition metal, A is one of A group elements, X is C and/or N; with n = 1, 2, or 3. The aim of this work is to exfoliate the MAX phases and produce 2D layers of transition metals carbides and/or nitrides by the selective etching of the A layers from the MAX phases. We labeled the resulting 2D M n+1Xn layers "MXenes" to emphasize the loss of the A group element from the MAX phases and the suffix "ene" to emphasize their 2D nature and their similarity to graphene. The etching process was carried out using aqueous hydrofluoric acid at room temperature. Thirteen different MXenes were produced as a result of this work, viz., Ti2C, Nb2C, V2C, Mo2C, (Ti0.5,Nb0.5)2C, (Ti 0.5,V0.5)2C, Ti3C2, (Ti 0.5,V0.5)3C2, (V0.5,Cr 0.5)3C2, Ti3CN, Ta4C 3, Nb4C3 and (Nb0.5,V0.5) 4C3. The as-synthesized MXenes were terminated with a mixture of OH, O, and/or F groups. Sonicating MXenes resulted in separating the stacked layers to a small extent. When Ti3C2 was intercalated with dimethylsulfoxide, however, followed by sonication in water, large-scale delamination occurred, which resulted in aqueous colloidal solutions that could in turn be fabricated into MXene "paper". MXenes were found to be electrically conductive, hydrophilic and stable in aqueous environments, a rare combination indeed, with huge potential in many applications, from energy storage, to sensors to catalysts. This work focused on the use of MXenes as electrode materials in Li

  7. A microwave synthesis of mesoporous NiCo2O4 nanosheets as electrode materials for lithium-ion batteries and supercapacitors.

    Science.gov (United States)

    Mondal, Anjon Kumar; Su, Dawei; Chen, Shuangqiang; Kretschmer, Katja; Xie, Xiuqiang; Ahn, Hyo-Jun; Wang, Guoxiu

    2015-01-12

    A facile microwave method was employed to synthesize NiCo2 O4 nanosheets as electrode materials for lithium-ion batteries and supercapacitors. The structure and morphology of the materials were characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy and Brunauer-Emmett-Teller methods. Owing to the porous nanosheet structure, the NiCo2 O4 electrodes exhibited a high reversible capacity of 891 mA h g(-1) at a current density of 100 mA g(-1) , good rate capability and stable cycling performance. When used as electrode materials for supercapacitors, NiCo2 O4 nanosheets demonstrated a specific capacitance of 400 F g(-1) at a current density of 20 A g(-1) and superior cycling stability over 5000 cycles. The excellent electrochemical performance could be ascribed to the thin porous structure of the nanosheets, which provides a high specific surface area to increase the electrode-electrolyte contact area and facilitate rapid ion transport.

  8. Highly enhanced electrochemical activity of Ni foam electrodes decorated with nitrogen-doped carbon nanotubes for non-aqueous redox flow batteries

    Science.gov (United States)

    Lee, Jungkuk; Park, Min-Sik; Kim, Ki Jae

    2017-02-01

    Nitrogen-doped carbon nanotubes (NCNTs) are directly grown on the surface of a three-dimensional (3D) Ni foam substrate by floating catalytic chemical vapor deposition (FCCVD). The electrochemical properties of the 3D NCNT-Ni foam are thoroughly examined as a potential electrode for non-aqueous redox flow batteries (RFBs). During synthesis, nitrogen atoms can be successfully doped onto the carbon nanotube (CNT) lattices by forming an abundance of nitrogen-based functional groups. The 3D NCNT-Ni foam electrode exhibits excellent electrochemical activities toward the redox reactions of [Fe (bpy)3]2+/3+ (in anolyte) and [Co(bpy)3]+/2+ (in catholyte), which are mainly attributed to the hierarchical 3D structure of the NCNT-Ni foam electrode and the catalytic effect of nitrogen atoms doped onto the CNTs; this leads to faster mass transfer and charge transfer during operation. As a result, the RFB cell assembled with 3D NCNT-Ni foam electrodes exhibits a high energy efficiency of 80.4% in the first cycle; this performance is maintained up to the 50th cycle without efficiency loss.

  9. Numerical and experimental evaluation of the relationship between porous electrode structure and effective conductivity of ions and electrons in lithium-ion batteries

    Science.gov (United States)

    Inoue, Gen; Kawase, Motoaki

    2017-02-01

    This study aims to develop a correlation equation between a porous electrode structure and the effective conductivity so as to design an optimal structure for a thick electrode layer of a high-capacity battery. We carried out a three-dimensional reconstruction of a lithium cobalt oxide and graphite electrode based on the cross-sectional images obtained via focused ion beam-scanning electron microscopy (FIB-SEM). The Li ion and electron conductivities are evaluated based on the effective conductive path determined from simulation and these values are compared with the experimental results obtained by electrochemical impedance spectroscopy carries out with a symmetric cell and the direct conductivity measurement under compression. Moreover, the amount of binder and the diameter of the active material particles are increased and decreased numerically using an actual reconstructed electrode structure, and the effect of those structures on the effective conductivity is examined. The most dominant factors that degrade ionic conductivity are the binder distribution and the particle morphology, respectively, in the cathode and anode, and a correlation equation with the function of porosity is obtained. These values are compared with those obtained by theoretical model equations, and the difference between the current effective ionic conductivity and the physical limiting value is determined.

  10. Influence of the structure of the anion in an ionic liquid electrolyte on the electrochemical performance of a silicon negative electrode for a lithium-ion battery

    Science.gov (United States)

    Yamaguchi, Kazuki; Domi, Yasuhiro; Usui, Hiroyuki; Shimizu, Masahiro; Matsumoto, Kuninobu; Nokami, Toshiki; Itoh, Toshiyuki; Sakaguchi, Hiroki

    2017-01-01

    We investigated the influence of the anions in ionic liquid electrolytes on the electrochemical performance of a silicon (Si) negative electrode for a lithium-ion battery. While the electrode exhibited poor cycle stability in tetrafluoroborate-based and propylene carbonate-based electrolytes, better cycle performance was achieved in bis(fluorosulfonyl)amide (FSA-)- and bis(trifluoromethanesulfonyl)amide (TFSA-)-based electrolytes, in which the discharge capacity of a Si electrode was more than 1000 mA h g-1 at the 100th cycle. It is considered that a surface film derived from FSA-- and TFSA--based electrolytes effectively suppressed continuous decomposition of the electrolyte. In a capacity limitation test, a discharge capacity of 1000 mA h g-1 was maintained even after about the 1600th cycle in the FSA--based electrolyte, which corresponds to a cycle life almost twice as long as that in TFSA--based electrolyte. This result should be explained by the high structural stability of FSA--derived surface film. In addition, better rate capability with a discharge capacity of 700 mA h g-1 was obtained at a high current rate of 6 C (21 A g-1) in FSA--based electrolyte, which was 7-fold higher than that in TFSA--based electrolyte. These results clarified that FSA--based ionic liquid electrolyte is the most promising candidate for Si-based negative electrodes.

  11. Beneficial effects of activated carbon additives on the performance of negative lead-acid battery electrode for high-rate partial-state-of-charge operation

    Science.gov (United States)

    Xiang, Jiayuan; Ding, Ping; Zhang, Hao; Wu, Xianzhang; Chen, Jian; Yang, Yusheng

    2013-11-01

    Experiments are made with negative electrode of 2 V cell and 12 V lead-acid battery doped with typical activated carbon additives. It turns out that the negative electrode containing tens-of-micron-sized carbon particles in NAM exhibits markedly increased HRPSoC cycle life than the one containing carbon particles with much smaller size of several microns or the one containing no activated carbon. The improved performance is mainly attributed to the optimized NAM microstructure and the enhanced electrode reaction kinetics by introducing appropriate activated carbon. The beneficial effects can be briefly summarized from three aspects. First, activated carbon acts as new porous-skeleton builder to increase the porosity and active surface of NAM, and thus facilitates the electrolyte diffusion from surface to inner and provides more sites for crystallization/dissolution of lead sulfate; second, activated carbon plays the role of electrolyte supplier to provide sufficient H2SO4 in the inner of plate when the diffusion of H2SO4 from plate surface cannot keep pace of the electrode reaction; Third, activated carbon acts as capacitive buffer to absorb excess charge current which would otherwise lead to insufficient NAM conversion and hydrogen evolution.

  12. Surface properties and graphitization of polyacrylonitrile based fiber electrodes affecting the negative half-cell reaction in vanadium redox flow batteries

    Science.gov (United States)

    Langner, J.; Bruns, M.; Dixon, D.; Nefedov, A.; Wöll, Ch.; Scheiba, F.; Ehrenberg, H.; Roth, C.; Melke, J.

    2016-07-01

    Carbon felt electrodes for vanadium redox flow batteries are obtained by the graphitization of polyacrylonitrile based felts at different temperatures. Subsequently, the surface of the felts is modified via thermal oxidation at various temperatures. A single-cell experiment shows that the voltage efficiency is increased by this treatment. Electrode potentials measured with reference electrode setup show that this voltage efficiency increase is caused mainly by a reduction of the overpotential of the negative half-cell reaction. Consequently, this reaction is investigated further by cyclic voltammetry and the electrode activity is correlated with structural and surface chemical properties of the carbon fibers. By Raman, X-ray photoelectron and near edge X-ray absorption fine structure spectroscopy the role of edge sites and oxygen containing functional groups (OCFs) for the electrochemical activity are elucidated. A significant activity increase is observed in correlation with these two characteristics. The amount of OCFs is correlated with structural defects (e.g. edge sites) of the carbon fibers and therefore decreases with an increasing graphitization degree. Thus, for the same thermal oxidation temperature carbon fibers graphitized at a lower temperature show higher activities than those graphitized at a higher temperature.

  13. LiNi 0.8 Co 0.2 O 2 -based high power lithium-ion battery positive electrodes analyzed by x-ray photoelectron spectroscopy: 1. Fresh electrode

    Energy Technology Data Exchange (ETDEWEB)

    Haasch, Richard T.; Abraham, Daniel A.

    2016-12-01

    High-power lithium-ion batteries are rapidly replacing the nickel metal hydride batteries currently used for energy storage in hybrid electric vehicles. Widespread commercialization of these batteries for vehicular applications is, however, limited by calendar-life performance, thermal abuse characteristics, and cost. The Advanced Technology Development Program was established by the U.S. Department of Energy to address these limitations. An important objective of this program was the development and application of diagnostic tools that provide unique ways to investigate the phenomena that limit lithium-ion cell life, performance, and safety characteristics. This report introduces a set of six Surface Science Spectra xray photoelectron spectroscopy (XPS) comparison records of data collected from positive electrodes (cathode) harvested from cylindrically wound, 18650-type, 1 A h capacity cells. The cathodes included in this study are (1) fresh, (2) following three formation cycles, (3) following calendar-life test for 12 weeks at 40 C, 60% state-of-charge (SOC), (4) following calendar-life test for 8 weeks at 50 C, 60% SOC, (5) following calendar-life test for 8 weeks at 60 C, 60% SOC, and (6) following calendar-life test for 2 weeks at 70 C, 60% SOC.

  14. Mechanical measurements on lithium phosphorous oxynitride coated silicon thin film electrodes for lithium-ion batteries during lithiation and delithiation

    Science.gov (United States)

    Al-Obeidi, Ahmed; Kramer, Dominik; Boles, Steven T.; Mönig, Reiner; Thompson, Carl V.

    2016-08-01

    The development of large stresses during lithiation and delithiation drives mechanical and chemical degradation processes (cracking and electrolyte decomposition) in thin film silicon anodes that complicate the study of normal electrochemical and mechanical processes. To reduce these effects, lithium phosphorous oxynitride (LiPON) coatings were applied to silicon thin film electrodes. Applying a LiPON coating has two purposes. First, the coating acts as a stable artificial solid electrolyte interphase. Second, it limits mechanical degradation by retaining the electrode's planar morphology during cycling. The development of stress in LiPON-coated electrodes was monitored using substrate curvature measurements. LiPON-coated electrodes displayed highly reproducible cycle-to-cycle behavior, unlike uncoated electrodes which had poorer coulombic efficiency and exhibited a continual loss in stress magnitude with continued cycling due to film fracture. The improved mechanical stability of the coated silicon electrodes allowed for a better investigation of rate effects and variations of mechanical properties during electrochemical cycling.

  15. Understanding the Size-Dependent Sodium Storage Properties of Na2C6O6-Based Organic Electrodes for Sodium-Ion Batteries.

    Science.gov (United States)

    Wang, Yaqun; Ding, Yu; Pan, Lijia; Shi, Ye; Yue, Zhuanghao; Shi, Yi; Yu, Guihua

    2016-05-11

    Organic electroactive materials represent a new generation of sustainable energy storage technology due to their unique features including environmental benignity, material sustainability, and highly tailorable properties. Here a carbonyl-based organic salt Na2C6O6, sodium rhodizonate (SR) dibasic, is systematically investigated for high-performance sodium-ion batteries. A combination of structural control, electrochemical analysis, and computational simulation show that rational morphological control can lead to significantly improved sodium storage performance. A facile antisolvent method was developed to synthesize microbulk, microrod, and nanorod structured SRs, which exhibit strong size-dependent sodium ion storage properties. The SR nanorod exhibited the best performance to deliver a reversible capacity of ∼190 mA h g(-1) at 0.1 C with over 90% retention after 100 cycles. At a high rate of 10 C, 50% of the capacity can be obtained due to enhanced reaction kinetics, and such high electrochemical activity maintains even at 80 °C. These results demonstrate a generic design route toward high-performance organic-based electrode materials for beyond Li-ion batteries. Using such a biomass-derived organic electrode material enables access to sustainable energy storage devices with low cost, high electrochemical performance and thermal stability.

  16. Toward highly stable solid-state unconventional thin-film battery-supercapacitor hybrid devices: Interfacing vertical core-shell array electrodes with a gel polymer electrolyte

    Science.gov (United States)

    Pandey, Gaind P.; Klankowski, Steven A.; Liu, Tao; Wu, Judy; Li, Jun

    2017-02-01

    A novel solid-state battery-supercapacitor hybrid device is fabricated for high-performance electrical energy storage using a Si anode and a TiO2 cathode in conjunction with a flexible, solid-like gel polymer electrolyte film as the electrolyte and separator. The electrodes were fabricated as three-dimensional nanostructured vertical arrays by sputtering active materials as conformal shells on vertically aligned carbon nanofibers (VACNFs) which serve as the current collector and structural template. Such nanostructured vertical core-shell array-electrodes enable short Li-ion diffusion path and large pseudocapacitive contribution by fast surface reactions, leading to the hybrid features of batteries and supercapacitors that can provide high specific energy over a wide range of power rates. Due to the improved mechanical stability of the infiltrated composite structure, the hybrid cell shows excellent cycling stability and is able to retain more than 95% of the original capacity after 3500 cycles. More importantly, this solid-state device can stably operate in a temperature range from -20 to 60 °C with a very low self-discharge rate and an excellent shelf life. This solid-state architecture is promising for the development of highly stable thin-film hybrid energy storage devices for unconventional applications requiring largely varied power, wider operation temperature, long shelf-life and higher safety standards.

  17. Free-standing electrodes composed of carbon-coated Li4Ti5O12 nanosheets and reduced graphene oxide for advanced sodium ion batteries

    Science.gov (United States)

    Xu, Guobao; Tian, Ye; Wei, Xiaolin; Yang, Liwen; Chu, Paul K.

    2017-01-01

    A free-standing electrode composed of carbon-coated Li4Ti5O12 nanosheets and reduced graphene oxide (designated as LTO-C/RGO) is fabricated for Na storage by modified vacuum filtration and subsequent annealing. In this process, graphene oxide with negative charges and LTO-C nanosheets with abundant charged ions are self-assembled into the nanocomposite based on the screening effect of electrostatic repulsion. The unique structure of the confined LTO-C nanosheets in a highly conductive interconnected RGO network not only promotes the reaction kinetics and structural stability of the electrodes during Na+ insertion/extraction, but also provides plenty of interfacial sites for Na+ adsorption giving rise to additional interfacial Na storage. The free-standing LTO-C/RGO anode for sodium ion battery exhibits a high capacity of 166 mAhg-1 at 1 C, good rate capability of 98.7 mAhg-1 at 5 C, and superior cyclic performance of 114 mAhg-1 at 2 C after 600 cycles. The materials boasting superior Na storage have large potential in high-performance sodium ion batteries in portable, flexible and wearable electronics.

  18. Thin film rechargeable electrodes based on conductive blends of nanostructured olivine LiFePO4 and sucrose derived nanocarbons for lithium ion batteries.

    Science.gov (United States)

    Praveen, P; Jyothsna, U; Nair, Priya; Ravi, Soumya; Balakrishnan, A; Subramanian, K R V; Nair, A Sreekumaran; Nair, V Shantikumar; Sivakumar, N

    2013-08-01

    The present study provides the first reports of a novel approach of electrophoretic co-deposition technique by which titanium foils are coated with LiFePO4-carbon nanocomposites synthesized by sol gel route and processed into high-surface area cathodes for lithium ion batteries. The study elucidates how sucrose additions as carbon source can affect the surface morphology and the redox reaction behaviors underlying these cathodes and thereby enhance the battery performance. The phase and morphological analysis were done using XRD and XPS where the LiFePO4 formed was confirmed to be a high purity orthorhombic system. From the analysis of the relevant electrochemical parameters using cyclic voltammetry and electrochemical impedance spectroscopy, a 20% increment and 90% decrement in capacity and impedance values were observed respectively. The composite electrodes also exhibited a specific capacity of 130 mA h/g. It has been shown that cathodes based on such composite systems can allow significant room for improvement in the cycling performance at the electrode/electrolyte interface.

  19. 锂离子液流电池电极悬浮液研究进展%Research progress of electrode suspensions of lithium-ion flow batteries

    Institute of Scientific and Technical Information of China (English)

    冯彩梅; 陈永翀; 韩立; 巩宇; Cserháti Csaba; Csik Attila

    2015-01-01

    The research progress in electrode suspensions of lithium-ion flow battery (LFB) was reviewed. LFB combines the working principles of lithium-ion battery and the structure characteristics of redox flow battery, with the independent power output and storage capacity, large energy density and comparatively low cost. LFB is suitable for the application in the future grid energy storage systems. For the LFB, the electrode suspension is one of the most important functional materials, because its conductive and rheological properties determine the energy density and rate performance of the battery. The technical bottlenecks and the research focuses were analyzed on the basis of the experimental data. The conductive mechanism, the specific capacity and the rheological properties are the important research contents of the electrode suspension for the establishment of a unified evaluation system.%锂离子液流电池将锂离子电池的工作原理与传统液流电池的结构特点相结合,是一种正处于基础技术开发阶段的新型电化学储能电池技术,具有输出功率和储能容量彼此独立、成本较低等特点,适用于未来电网储能领域。电极悬浮液作为实现锂离子液流电池充放电功能的主体材料,其导电性能和流动性能是影响锂离子液流电池倍率特性和能量密度的重要因素。论文结合实验数据对该方向面临的主要技术问题及研究重点进行了分析,认为电极悬浮液的研究需要从导电机理、质量比容量、流变性能等方面进一步深入研究,并建立标准评价体系。

  20. Li distribution characterization in Li-ion batteries positive electrodes containing LixNi0.8Co0.15Al0.05O2 secondary particles (0.75 ⩽ x ⩽ 1.0)

    Science.gov (United States)

    Mima, K.; Gonzalez-Arrabal, R.; Azuma, H.; Yamazaki, A.; Okuda, C.; Ukyo, Y.; Sawada, H.; Fujita, K.; Kato, Y.; Perlado, J. M.; Nakai, S.

    2012-11-01

    The elemental distribution of as-received (non-charged) and charged Li-ion battery positive electrodes containing LixNi0.8Co0.15Al0.05O2 (0.75 ⩽ x ⩽ 1.0) microparticles as active material is characterized by combining μ-PIXE and μ-PIGE techniques. PIGE measurements evidence that the Li distribution is inhomogeneous (existence of Li-rich and Li-depleted regions) in as-received electrodes corresponding with the distribution of secondary particles but it is homogeneous within the studied individual secondary micro-particles. The dependence of the Li distribution on electrode thickness and on charging conditions is characterized by measuring the Li distribution maps in specifically fabricated cross-sectional samples. These data show that decreasing the electrode thickness down to 35 μm and charging the batteries at slow rate give rise to more homogeneous Li depth profiles.

  1. Mathematical Modeling of Electrolyte Flow Dynamic Patterns and Volumetric Flow Penetrations in the Flow Channel over Porous Electrode Layered System in Vanadium Flow Battery with Serpentine Flow Field Design

    OpenAIRE

    Ke, Xinyou; Prahl, Joseph M.; Alexander, J. Iwan D.; Savinell, Robert F.

    2016-01-01

    In this work, a two-dimensional mathematical model is developed to study the flow patterns and volumetric flow penetrations in the flow channel over the porous electrode layered system in vanadium flow battery with serpentine flow field design. The flow distributions at the interface between the flow channel and porous electrode are examined. It is found that the non-linear pressure distributions can distinguish the interface flow distributions under the ideal plug flow and ideal parabolic fl...

  2. Synthesis, Characterization and Density Functional Study of LiMn1.5Ni 0.5O4 Electrode for Lithium ion Battery

    Directory of Open Access Journals (Sweden)

    M. Aruna Bharathi

    2014-04-01

    Full Text Available This paper analyses material issues of development of Li-ion batteries to store electrical energy. The performance of the battery is improved by developing the high energy density cathode materials at Nano level. This paper explains the synthesis of most interesting cathode material Lithium Manganese Spinel and its derivatives like transition metal oxide (LiNi0.5Mn1.5O4 using Co-Precipitation chemical method; it is one of the eco-friendly ,effective, economic and easy preparation method. The structural features of LiNi0.5Mn1.5O4 was characterized by XRD – analysis indicated that prepared sample mainly belong to cubic crystal form with Fd3m space group ,with lattice parameter a  8.265 and average crystal size of 31.59 nm and compared the experimental results with computation details from first principle computation methods with Quantum wise Atomistix Tool Kit (ATK,Virtual Nano Lab. First principle computation methods provide important role in emerging and optimizing this electrode material. In this study we present an overview of the computation approach aimed at building LiNi0.5Mn1.5O4 crystal as cathode for Lithium ion battery. We show each significant property can be related to the structural component in the material and can be computed from first principle. By direct comparison with experimental results, we assume to interpret that first principle computation can help to accelerate the design & development of LiNi0.5Mn1.5O4 as cathode material of lithium ion battery for energy storage.

  3. Ionic Liquid-Organic Carbonate Electrolyte Blends To Stabilize Silicon Electrodes for Extending Lithium Ion Battery Operability to 100 °C.

    Science.gov (United States)

    Ababtain, Khalid; Babu, Ganguli; Lin, Xinrong; Rodrigues, Marco-Tulio F; Gullapalli, Hemtej; Ajayan, Pulickel M; Grinstaff, Mark W; Arava, Leela Mohana Reddy

    2016-06-22

    Fabrication of lithium-ion batteries that operate from room temperature to elevated temperatures entails development and subsequent identification of electrolytes and electrodes. Room temperature ionic liquids (RTILs) can address the thermal stability issues, but their poor ionic conductivity at room temperature and compatibility with traditional graphite anodes limit their practical application. To address these challenges, we evaluated novel high energy density three-dimensional nano-silicon electrodes paired with 1-methyl-1-propylpiperidinium bis(trifluoromethanesulfonyl)imide (Pip) ionic liquid/propylene carbonate (PC)/LiTFSI electrolytes. We observed that addition of PC had no detrimental effects on the thermal stability and flammability of the reported electrolytes, while largely improving the transport properties at lower temperatures. Detailed investigation of the electrochemical properties of silicon half-cells as a function of PC content, temperature, and current rates reveal that capacity increases with PC content and temperature and decreases with increased current rates. For example, addition of 20% PC led to a drastic improvement in capacity as observed for the Si electrodes at 25 °C, with stability over 100 charge/discharge cycles. At 100 °C, the capacity further increases by 3-4 times to 0.52 mA h cm(-2) (2230 mA h g(-1)) with minimal loss during cycling.

  4. Tuning the Activity of Oxygen in LiNi0.8Co0.15Al0.05O2 Battery Electrodes.

    Science.gov (United States)

    Karki, Khim; Huang, Yiqing; Hwang, Sooyeon; Gamalski, Andrew D; Whittingham, M Stanley; Zhou, Guangwen; Stach, Eric A

    2016-10-06

    Layered transition metal oxides such as LiNi0.8Co 0.15Al0.05O2 (NCA) are highly desirable battery electrodes. However, these materials suffer from thermal runaway caused by deleterious oxygen loss and surface phase transitions when in highly overcharged and overheated conditions, prompting serious safety concerns. Using in situ environmental transmission electron microscopy techniques, we demonstrate that surface oxygen loss and structural changes in the highly overcharged NCA particles are suppressed by exposing them to an oxygen-rich environment. The onset temperature for the loss of oxygen from the electrode particle is delayed to 350 °C at oxygen gas overpressure of 400 mTorr. Similar heating of the particles in a reducing hydrogen gas demonstrated a quick onset of oxygen loss at 150 °C and rapid surface degradation of the particles. The results reported here illustrate the fundamental mechanism governing the failure processes of electrode particles and highlight possible strategies to circumvent such issues.

  5. Polyoxometalate flow battery

    Science.gov (United States)

    Anderson, Travis M.; Pratt, Harry D.

    2016-03-15

    Flow batteries including an electrolyte of a polyoxometalate material are disclosed herein. In a general embodiment, the flow battery includes an electrochemical cell including an anode portion, a cathode portion and a separator disposed between the anode portion and the cathode portion. Each of the anode portion and the cathode portion comprises a polyoxometalate material. The flow battery further includes an anode electrode disposed in the anode portion and a cathode electrode disposed in the cathode portion.

  6. Performance study of magnesium-sulfur battery using a graphene based sulfur composite cathode electrode and a non-nucleophilic Mg electrolyte

    Science.gov (United States)

    Vinayan, B. P.; Zhao-Karger, Zhirong; Diemant, Thomas; Chakravadhanula, Venkata Sai Kiran; Schwarzburger, Nele I.; Cambaz, Musa Ali; Behm, R. Jürgen; Kübel, Christian; Fichtner, Maximilian

    2016-02-01

    Here we report for the first time the development of a Mg rechargeable battery using a graphene-sulfur nanocomposite as the cathode, a Mg-carbon composite as the anode and a non-nucleophilic Mg based complex in tetraglyme solvent as the electrolyte. The graphene-sulfur nanocomposites are prepared through a new pathway by the combination of thermal and chemical precipitation methods. The Mg/S cell delivers a higher reversible capacity (448 mA h g-1), a longer cyclability (236 mA h g-1 at the end of the 50th cycle) and a better rate capability than previously described cells. The dissolution of Mg polysulfides to the anode side was studied by X-ray photoelectron spectroscopy. The use of a graphene-sulfur composite cathode electrode, with the properties of a high surface area, a porous morphology, a very good electronic conductivity and the presence of oxygen functional groups, along with a non-nucleophilic Mg electrolyte gives an improved battery performance.Here we report for the first time the development of a Mg rechargeable battery using a graphene-sulfur nanocomposite as the cathode, a Mg-carbon composite as the anode and a non-nucleophilic Mg based complex in tetraglyme solvent as the electrolyte. The graphene-sulfur nanocomposites are prepared through a new pathway by the combination of thermal and chemical precipitation methods. The Mg/S cell delivers a higher reversible capacity (448 mA h g-1), a longer cyclability (236 mA h g-1 at the end of the 50th cycle) and a better rate capability than previously described cells. The dissolution of Mg polysulfides to the anode side was studied by X-ray photoelectron spectroscopy. The use of a graphene-sulfur composite cathode electrode, with the properties of a high surface area, a porous morphology, a very good electronic conductivity and the presence of oxygen functional groups, along with a non-nucleophilic Mg electrolyte gives an improved battery performance. Electronic supplementary information (ESI) available

  7. A density functional theory study of the carbon-coating effects on lithium iron borate battery electrodes.

    Science.gov (United States)

    Loftager, Simon; García-Lastra, Juan María; Vegge, Tejs

    2017-01-18

    Lithium iron borate (LiFeBO3) is a promising cathode material due to its high theoretical specific capacity, inexpensive components and small volume change during operation. Yet, challenges related to severe air- and moisture-induced degradation have prompted the utilization of a protective coating on the electrode which also improves the electronic conductivity. However, not much is known about the preferential geometries of the coating as well as how these coating-electrode interfaces influence the lithium diffusion between the coating and the electrode. Here, we therefore present a density functional theory (DFT) study of the anchoring configurations of carbon coating on the LiFeBO3 electrode and its implications on the interfacial lithium diffusion. Due to large barriers associated with Li-ion diffusion through a parallel-oriented pristine graphene coating on the FeBO3 and LiFeBO3 electrode surfaces, large structural defects in the graphene coating are required for fast Li-ion diffusion. However, such defects are expected to exist only in small concentrations due to their high formation energies. Alternative coating geometries were therefore investigated, and the configuration in which the coating layers were anchored normal to the electrode surface at B and O atoms was found to be most stable. Nudged elastic band (NEB) calculations of the lithium diffusion barriers across the interface between the optimally oriented coating layers and the electrode show no kinetic limitations for lithium extraction and insertion. Additionally, this graphite-coating configuration showed partial blocking of electrode-degrading species.

  8. Integrated fast assembly of free-standing lithium titanate/carbon nanotube/cellulose nanofiber hybrid network film as flexible paper-electrode for lithium-ion batteries.

    Science.gov (United States)

    Cao, Shaomei; Feng, Xin; Song, Yuanyuan; Xue, Xin; Liu, Hongjiang; Miao, Miao; Fang, Jianhui; Shi, Liyi

    2015-05-27

    A free-standing lithium titanate (Li4Ti5O12)/carbon nanotube/cellulose nanofiber hybrid network film is successfully assembled by using a pressure-controlled aqueous extrusion process, which is highly efficient and easily to scale up from the perspective of disposable and recyclable device production. This hybrid network film used as a lithium-ion battery (LIB) electrode has a dual-layer structure consisting of Li4Ti5O12/carbon nanotube/cellulose nanofiber composites (hereinafter referred to as LTO/CNT/CNF), and carbon nanotube/cellulose nanofiber composites (hereinafter referred to as CNT/CNF). In the heterogeneous fibrous network of the hybrid film, CNF serves simultaneously as building skeleton and a biosourced binder, which substitutes traditional toxic solvents and synthetic polymer binders. Of importance here is that the CNT/CNF layer is used as a lightweight current collector to replace traditional heavy metal foils, which therefore reduces the total mass of the electrode while keeping the same areal loading of active materials. The free-standing network film with high flexibility is easy to handle, and has extremely good conductivity, up to 15.0 S cm(-1). The flexible paper-electrode for LIBs shows very good high rate cycling performance, and the specific charge/discharge capacity values are up to 142 mAh g(-1) even at a current rate of 10 C. On the basis of the mild condition and fast assembly process, a CNF template fulfills multiple functions in the fabrication of paper-electrode for LIBs, which would offer an ever increasing potential for high energy density, low cost, and environmentally friendly flexible electronics.

  9. Liquid-metal electrode to enable ultra-low temperature sodium-beta alumina batteries for renewable energy storage.

    Science.gov (United States)

    Lu, Xiaochuan; Li, Guosheng; Kim, Jin Y; Mei, Donghai; Lemmon, John P; Sprenkle, Vincent L; Liu, Jun

    2014-01-01

    Commercial sodium-sulphur or sodium-metal halide batteries typically need an operating temperature of 300-350 °C, and one of the reasons is poor wettability of liquid sodium on the surface of beta alumina. Here we report an alloying strategy that can markedly improve the wetting, which allows the batteries to be operated at much lower temperatures. Our combined experimental and computational studies suggest that addition of caesium to sodium can markedly enhance the wettability. Single cells with Na-Cs alloy anodes exhibit great improvement in cycling life over those with pure sodium anodes at 175 and 150 °C. The cells show good performance even at as low as 95 °C. These results demonstrate that sodium-beta alumina batteries can be operated at much lower temperatures with successfully solving the wetting issue. This work also suggests a strategy to use liquid metals in advanced batteries that can avoid the intrinsic safety issues associated with dendrite formation.

  10. On the Zinc Air Battery Electrode Surface Seepage Phenomenon%锌空气电池电极表面渗液现象的研究

    Institute of Scientific and Technical Information of China (English)

    杨永青; 徐献芝; 李清宇; 刘晓毅

    2012-01-01

    渗液问题是锌空气电池的主要问题之一.本文通过如下实验:聚四氟乙烯膜(PTFE,poly tetra fluoro ethylene)表面特性实验、电池风冷放电、空气电极电压实验和类列斯实验,对可能影响电池渗液的因素进行了研究.这些因素包括:PTFE膜、温度、电压、电荷总量、电解质溶液.实验结果表明:PTFE膜经过KOH溶液浸泡一段时间后,其接触角会显著变小,疏水性变差;温度和电压会对渗液现象产生影响;在各类电解质溶液中,KOH溶液渗液最严重;放电过程中的电荷总量对渗液问题基本没影响.实验结果分析得出,这类电池渗液主要是由于上述因素导致电解液表面张力变化,引起气液界面移动导致的.%Seepage is one of the main problems of zinc air battery. Factors that may affect the battery seepage were investigated through following experiments: PTFE (poly tetra fluoro ethylene) film surface properties experiment, battery cooling discharge experiment, air electrode voltage experiment and Antilliean electro-osmosis test. These involved factors include PTFE film, temperature, voltaget charge quantity and electrolyte solution. Experimental results show that after soak in KOH solution for a period of time, the contact angle of PTFE film becomes significantly small and its hydrophobic property deteriorates; temperature and voltage indeed have influence on seepage phenomenon; KOH solution seepage is the most serious in all kinds of electrolyte solution) the total charge in discharge process basically has no influence on seepage. Based on analysis of experimental results, it is concluded that the battery seepage is caused by the change of electrolyte solution surface tension induced by above factors, which results in gas-liquid interface movement, Above results are valuable for improving the performance of zinc air battery.

  11. Mesoporous MnCo2O4 with a flake-like structure as advanced electrode materials for lithium-ion batteries and supercapacitors.

    Science.gov (United States)

    Mondal, Anjon Kumar; Su, Dawei; Chen, Shuangqiang; Ung, Alison; Kim, Hyun-Soo; Wang, Guoxiu

    2015-01-19

    A mesoporous flake-like manganese-cobalt composite oxide (MnCo2O4) is synthesized successfully through the hydrothermal method. The crystalline phase and morphology of the materials are characterized by X-ray diffraction, field-emission scanning electron microscopy, transmission electron microscopy, and Brunauer-Emmett-Teller methods. The flake-like MnCo2O4 is evaluated as the anode material for lithium-ion batteries. Owing to its mesoporous nature, it exhibits a high reversible capacity of 1066 mA h g(-1), good rate capability, and superior cycling stability. As an electrode material for supercapacitors, the flake-like MnCo2O4 also demonstrates a high supercapacitance of 1487 F g(-1) at a current density of 1 A g(-1), and an exceptional cycling performance over 2000 charge/discharge cycles.

  12. Mathematical Modeling of Electrolyte Flow Dynamic Patterns and Volumetric Flow Penetrations in the Flow Channel over Porous Electrode Layered System in Vanadium Flow Battery with Serpentine Flow Field Design

    CERN Document Server

    Ke, Xinyou; Alexander, J Iwan D; Savinell, Robert F

    2016-01-01

    In this work, a two-dimensional mathematical model is developed to study the flow patterns and volumetric flow penetrations in the flow channel over the porous electrode layered system in vanadium flow battery with serpentine flow field design. The flow distributions at the interface between the flow channel and porous electrode are examined. It is found that the non-linear pressure distributions can distinguish the interface flow distributions under the ideal plug flow and ideal parabolic flow inlet boundary conditions. However, the volumetric flow penetration within the porous electrode beneath the flow channel through the integration of interface flow velocity reveals that this value is identical under both ideal plug flow and ideal parabolic flow inlet boundary conditions. The volumetric flow penetrations under the advection effects of flow channel and landing/rib are estimated. The maximum current density achieved in the flow battery can be predicted based on the 100% amount of electrolyte flow reactant ...

  13. Microstructure formation of lithium-ion battery electrodes during drying - An ex-situ study using cryogenic broad ion beam slope-cutting and scanning electron microscopy (Cryo-BIB-SEM)

    Science.gov (United States)

    Jaiser, Stefan; Kumberg, Jana; Klaver, Jop; Urai, Janos L.; Schabel, Wilhelm; Schmatz, Joyce; Scharfer, Philip

    2017-03-01

    Properties of lithium-ion battery electrodes relate to the complex microstructure that develops during solvent removal. We use cryogenic scanning electron microscopy in combination with broad ion beam slope-cutting (Cryo-BIB-SEM) for the ex-situ imaging of film formation in battery electrodes. Drying of anode films is quenched by cryo-preservation in slushy nitrogen at systematically increasing drying times, followed by SEM imaging under cryogenic conditions. Energy dispersive x-ray spectroscopy (EDS) and image processing of segmented cross-sections are used to analyze the development of component gradients with time. We find electrode films to shrink homogeneously and not in a top-down consolidation process as previously hypothesized. Binder gradients evolve in the liquid phase and initiate solvent diffusion from the bulk to the surface, thereby dragging binder towards the surface. Capillary transport is identified as a fundamental process that directly impacts drying kinetics and binder distribution.

  14. LiCoO2 electrode/electrolyte interface of Li-ion batteries investigated by electrochemical impedance spectroscopy

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    The storage behavior and the first delithiation of LiCoO2 electrode in 1 mol/L LiPF6-EC:DMC:DEC electrolyte were investigated by electrochemical impedance spectroscopy (EIS). It has found that, along with the increase of storage time, the thickness of SEI film increases, and some organic carbonate lithium compounds are formed due to spontaneous reactions occurring between the LiCoO2 electrode and the electrolyte. When electrode potential is changed from 3.8 to 3.95 V, the reversible breakdown of the resistive SEI film occurs, which is attributed to the reversible dissolution of the SEI film component. With the increase of electrode potential, the thickness of SEI film increases rapidly above 4.2 V, due to overcharge reactions. The inductive loop observed in impedance spectra of the LiCoO2 electrode in Li/LiCoO2 cells is attributed to the formation of a Li1-xCoO2/LiCoO2 concentration cell. Moreover, it has been demonstrated that the lithium-ion insertion-deinsertion in LiCoO2 hosts can be well described by both Langmuir and Frumkin insertion isotherms, and the symmetry factor of charge transfer has been evaluated at 0.5.

  15. Superior cycle stability and high rate capability of Zn-Al-In-hydrotalcite as negative electrode materials for Ni-Zn secondary batteries

    Science.gov (United States)

    Wang, Ruijuan; Yang, Zhanhong; Yang, Bin; Wang, Tingting; Chu, Zhihao

    2014-04-01

    Zn-Al-In layered double hydroxides (LDHs) are synthesized by hydrothermal method and investigated as negative electrode materials for Ni-Zn batteries. The Fourier transform infrared spectra (FT-IR), X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM) images show the as-prepared samples are well-crystallized and hexagon structure. The electrochemical performances of Zn-Al-LDHs and Zn-Al-In-LDHs with different Zn/Al/In molar ration are investigated by the cyclic voltammograms (CV), Tafel polarization and galvanostatic charge-discharge measurements. Zn-Al-LDHs shows good stability in the first 300-cycles. However, during the subsequent cycles, the discharge capacity decreases with increasing of the cycles. Compared with Zn-Al-LDHs, Zn-Al-In-LDHs with different Zn/Al/In molar rations, especially the sample of Zn/Al/In = 3:0.75:0.25 (molar ration) have higher discharge capacity and more stable cycling performances. This battery can undergo at least 800 charge-discharge cycles at constant current of 1C without dendrite and short circuits. The discharge capacity of Zn-Al-In-LDHs after the 800th cycle remains about 380 mAh g-1. Zn-Al-In-LDHs possess a high rate capability to meet the needs of high-storage applications.

  16. 锂离子电池碳负极材料研究进展%Advances of Negative Electrode Material for Lithium Ion Battery

    Institute of Scientific and Technical Information of China (English)

    孙学亮; 秦秀娟; 卜立敏; 吴伟

    2011-01-01

    The latest research advances on carbon anode materials for Li-ion batteries are reviewed. The MCMB, natural graphite, amorphous carbon materials and surface modification of natural graphite are included. Surface modification of natural graphite is an important means to improve the anode material properties of Li-ion battery. Through the modified treatment, the irreversible capacity of graphite electrode can be effectively reduced, so that the reversible capacity and coulomb efficiency have a great degree of improvement. On account of surface modification of natural graphite possess general advantages of cost and performance, in future it will be the main Li-ion battery anode materials in industrial applications.%综述锂离子电池碳负极材料的研究进展,主要包括中间相碳微球、天然石墨、无定形碳负极材料以及天然石墨表面改性.对天然石墨表面改性是改善锂离子电池负极材料性能的重要手段,通过改性处理,可有效降低石墨电极的不可逆容量,从而使可逆容最和库仑效率有较大程度的提高.由于表面改性天然石墨具有成本和性能方面的综合优势,是今后较长一段时间内,工业化应用的锂离子电池主要负极材料.

  17. Effect of Porosity on the Thick Electrodes for High Energy Density Lithium Ion Batteries for Stationary Applications

    Directory of Open Access Journals (Sweden)

    Madhav Singh

    2016-11-01

    Full Text Available A series of 250–350 μ m-thick single-sided lithium ion cell graphite anodes and lithium nickel manganese cobalt oxide (NMC cathodes with constant area weight, but varying porosity were prepared. Over this wide thickness range, micron-sized carbon fibers were used to stabilize the electrode structure and to improve electrode kinetics. By choosing the proper porosities for the anode and cathode, kinetic limitations and aging losses during cell cycling could be minimized and energy density improved. The cell (C38%-A48% exhibits the highest energy density, 441 Wh/L at the C/10 rate, upon cycling at elevated temperature and different C-rates. The cell (C38%-A48% showed 9% higher gravimetric energy density at C/10 in comparison to the cell with as-coated electrodes.

  18. The self-discharge mechanism of AB{sub 5}-type hydride electrodes in Ni/MH batteries

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Chunsheng [Center for Manufacturing Research and Department of Chemical Engineering, Tennessee Technological University, Cookeville, TN 38505 (United States); Marrero-Rivera, Mariza; Serafini, Daniel A.; Baricuatro, Jack H.; Soriaga, Manuel P. [Department of Chemistry, Texas A and M University, College Station, TX 77843 (United States); Srinivasan, Supramaniam [Center for Energy and Environmental Studies, Princeton University, Princeton, NJ 08544 (United States)

    2006-04-15

    A new strategy in the study of the self-discharge mechanism of metal-hydride electrodes has been developed. The self-discharge behavior of a LaNi{sub 3.55}Co{sub 0.75}Mn{sub 0.4}Al{sub 0.3} electrode in alkaline solution, with and without ZnO additive, was investigated. Experimental results showed that the self-discharge rate (hydrogen desorption) within the single-phase region is controlled by the difference between the equilibrium hydrogen partial pressure at the electrode and the actual hydrogen partial pressure in the cell. Dissolved oxygen was also found to exert a strong influence on the self-discharge rate in the single-phase region. In the two-phase region, the self-discharge is limited by the rate of phase transformation. A four-step mechanism for the self-discharge process is proposed. (author)

  19. A density functional theory study of the carbon-coating effects on lithium iron borate battery electrodes

    DEFF Research Database (Denmark)

    Loftager, Simon; García Lastra, Juan Maria; Vegge, Tejs

    2016-01-01

    a density functional theory (DFT) study of the anchoring configurations of carbon coating on the LiFeBO3 electrode and its implications on the interfacial lithium diffusion. Due to large barriers associated with Li-ion diffusion through a parallel-oriented pristine graphene coating on the FeBO3 and LiFeBO3...... electrode surfaces, large structural defects in the graphene coating are required for fast Li-ion diffusion. However, such defects are expected to exist only in small concentrations due to their high formation energies. Alternative coating geometries were therefore investigated, and the configuration...

  20. A density functional theory study of the carbon-coating effects on lithium iron borate battery electrodes

    DEFF Research Database (Denmark)

    Loftager, Simon; García Lastra, Juan Maria; Vegge, Tejs

    2017-01-01

    a density functional theory (DFT) study of the anchoring configurations of carbon coating on the LiFeBO3 electrode and its implications on the interfacial lithium diffusion. Due to large barriers associated with Li-ion diffusion through a parallel-oriented pristine graphene coating on the FeBO3 and LiFeBO3...... electrode surfaces, large structural defects in the graphene coating are required for fast Li-ion diffusion. However, such defects are expected to exist only in small concentrations due to their high formation energies. Alternative coating geometries were therefore investigated, and the configuration...

  1. Glyoxalated polyacrylamide as a covalently attachable and rapidly cross-linkable binder for Si electrode in lithium ion batteries

    Science.gov (United States)

    Yoo, Jung-Keun; Jeon, Jaebeom; Kang, Kisuk; Jung, Yeon Sik

    2017-03-01

    Recently, investigation of Si-based anode materials for rechargeable battery applications garnered much interest due to its exceptionally high capacity. High-capacity Si anode ( 4,200 mAhg-1) is highly desirable for the replacement of conventional graphite anode (batteries. We herein demonstrate highly cross-linked polymeric binder (glyoxalated polyacrylamide) with an enhanced mechanical property by applying wet-strengthening chemistry used in paper industry. We found that the degree of cross-linking can be systematically adjusted by controlling the acidity of the slurry and has a profound effect on the cell performance using Si anode. The enhanced cycle performance of Si nanoparticles obtained by treating the binder at pH 4 can be explained by its strong interaction between the binder and Si surface and current collector, and also rigidity of binder by cross-linking.

  2. Study of AB{sub 2} alloy electrodes for Ni/MH battery prepared by centrifugal casting and gas atomization

    Energy Technology Data Exchange (ETDEWEB)

    Young, K., E-mail: kwoyoung@yahoo.co [Energy Conversion Devices Inc./Ovonic Battery Company, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Koch, J.; Ouchi, T. [Energy Conversion Devices Inc./Ovonic Battery Company, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States); Banik, A. [Special Metal Corporation, 100 Industry Lane, Princeton, KY 42445 (United States); Fetcenko, M.A. [Energy Conversion Devices Inc./Ovonic Battery Company, 2983 Waterview Drive, Rochester Hills, MI 48309 (United States)

    2010-04-30

    Centrifugal casting and gas atomization processes were applied on multiple phase AB{sub 2} alloys and compared to the conventional melt-and-cast. Four different compositions were chosen for this study. The roles of Zr, Mn, Cr, and Ni in various battery aspects are identified. Cooling speed was found to be crucial for the C14 and C15 phase abundances. As the cooling speed increased from 10{sup 2} to 10{sup 4} degrees per second, a higher percentage of C15 was found. The centrifugal casting process provided better cycle life and low temperature performance with the only trade-off being slower activation. The gas atomization process can achieve lower production cost due to the elimination of a grinding procedure and extended cycle life, but suffers from higher bulk oxygen content and thicker surface oxide, and thus inferior in all battery performance characteristics other than cycle life and charge retention.

  3. Alkylphosphate-based nonflammable gel electrolyte for LiMn{sub 2}O{sub 4} positive electrode in lithium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Yoshimoto, Nobuko; Gotoh, Daisuke; Egashira, Minato; Morita, Masayuki [Graduate School of Science and Engineering, Yamaguchi University, 2-16-1 Tokiwadai, Ube 755-8611 (Japan)

    2008-12-01

    Polymeric gel containing alkylphosphate has been examined as nonflammable gel electrolyte for LiMn{sub 2}O{sub 4} positive electrode of lithium-ion battery (LIB). The gel was composed of a polymer matrix of poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-HFP) and a liquid component consisting of ternary solvent of trimethyl phosphate (TMP) mixed with ethylene carbonate (EC) and diethyl carbonate (DEC) that dissolves lithium salt (LiPF{sub 6} or LiBF{sub 4}). The gel composition of 0.8 M (mol dm{sup -3}) LiX (X = PF{sub 6} and BF{sub 4}) dissolved in EC + DEC + TMP (55:25:20) with PVdF-HFP showed excellent nonflammable characteristics and high ionic conductivity of ca. 3.1 mS cm{sup -1} at room temperature (20 C). The charge-discharge cycling test of LiMn{sub 2}O{sub 4} positive electrode gave good reversibility with high capacitance in the gel electrolyte. With respect to the electrolyte salt, LiBF{sub 4} was better than LiPF{sub 6} due to its thermal stability during the gel preparation. (author)

  4. Preparation, structure, and electrochemistry of layered polyanionic hydroxysulfates: LiMSO4OH (M = Fe, Co, Mn) electrodes for Li-ion batteries.

    Science.gov (United States)

    Subban, Chinmayee V; Ati, Mohamed; Rousse, Gwenaëlle; Abakumov, Artem M; Van Tendeloo, Gustaaf; Janot, Raphaël; Tarascon, Jean-Marie

    2013-03-01

    The Li-ion rechargeable battery, due to its high energy density, has driven remarkable advances in portable electronics. Moving toward more sustainable electrodes could make this technology even more attractive to large-volume applications. We present here a new family of 3d-metal hydroxysulfates of general formula LiMSO4OH (M = Fe, Co, and Mn) among which (i) LiFeSO4OH reversibly releases 0.7 Li(+) at an average potential of 3.6 V vs Li(+)/Li(0), slightly higher than the potential of currently lauded LiFePO4 (3.45 V) electrode material, and (ii) LiCoSO4OH shows a redox activity at 4.7 V vs Li(+)/Li(0). Besides, these compounds can be easily made at temperatures near 200 °C via a synthesis process that enlists a new intermediate phase of composition M3(SO4)2(OH)2 (M = Fe, Co, Mn, and Ni), related to the mineral caminite. Structurally, we found that LiFeSO4OH is a layered phase unlike the previously reported 3.2 V tavorite LiFeSO4OH. This work should provide an impetus to experimentalists for designing better electrolytes to fully tap the capacity of high-voltage Co-based hydroxysulfates, and to theorists for providing a means to predict the electrochemical redox activity of two polymorphs.

  5. A numerical model for a soluble lead-acid flow battery comprising a three-dimensional honeycomb-shaped positive electrode

    Science.gov (United States)

    Oury, Alexandre; Kirchev, Angel; Bultel, Yann

    2014-01-01

    A novel reactor design is proposed for the soluble lead-acid flow battery (SLFB), in which a three-dimensional honeycomb-shaped positive PbO2-electrode is sandwiched between two planar negative electrodes. A two-dimensional stationary model is developed to predict the electrochemical behaviour of the cell, especially the current distribution over the positive structure and the cell voltage, as a function of the honeycomb dimensions and the electrolyte composition. The model includes several experimentally-based parameters measured over a wide range of electrolyte compositions. The results show that the positive current distribution is almost entirely determined by geometrical effects, with little influence from the hydrodynamic. It is also suggested that an increase in the electrolyte acidity diminishes the overvoltage during discharge but leads at the same time to a more heterogeneous reaction rate distribution on account of the faster kinetics of PbO2 dissolution. Finally, the cycling of experimental mono-cells is performed and the voltage response is in fairly good accordance with the model predictions.

  6. The Influence of Electrode Microstructure on the Performance of Free-Standing Cathode for Aprotic Lithium-Oxygen Battery

    Science.gov (United States)

    Shen, Chen; Wen, Zhaoyin; Wang, Fan; Wu, Xiangwei; Chen, Chunhua

    2016-10-01

    Free-standing NiCo2O4@Ni cathodes for aprotic lithium-oxygen batteries were synthesized through a simple hydrothermal process followed by heat treatment in the air. The morphology of the NiCo2O4 deposit changed from nanosheet to nanowire with the increase of hydrothermal time. Further observation revealed that the nanosheet/nanowire NiCo2O4 were assembled by nanoparticles with a size of 10-20 nm. The directional assembly of the nanoparticles were not affected by the reaction time. The influence of catalyst microstructure on the electrochemical performance of Li-O2 batteries was studied. The results of battery tests in pure oxygen indicate that the cathode material with a high specific surface area, large pore volume and broad pore size distribution can facilitate the discharge reaction, leading to an improved cell performance. As a result, the cathode based on the NiCo2O4 nanowire array delivered a specific discharge capacity of 1682 mAh g-1 at 30 mA g-1 and a stable cyclability of 50 cycles with a capacity limitation of 500 mAh g-1.

  7. Simultaneous fluorination of active material and conductive agent for improving the electrochemical performance of LiNi0.5Mn1.5O4 electrode for lithium-ion batteries

    Science.gov (United States)

    Song, Min Sang; Kim, Dae Sik; Park, Eunjun; Choi, Jae Man; Kim, Hansu

    2016-09-01

    High-voltage cathode materials have gained much attention as one of the promising electrode materials to increase power density of lithium ion batteries by raising the working voltage. However, the use of such high-voltage cathode materials is still challenging, because their working voltage is close to the electrochemical oxidation potential of organic electrolyte used in lithium ion batteries. In this work, we demonstrated that simultaneous fluorination of LiNi0.5Mn1.5O4 (LNMO) particles as well as conductive agent in the electrode could significantly improve the electrochemical stability of LNMO cathode. The resulting electrode showed better cycle performance both at room temperature and elevated temperature compared to both bare LNMO electrode and the electrode with only LNMO fluorinated. These results showed that direct fluorination of high voltage cathode can reduce the side reaction of high voltage cathode electrode with the electrolyte, thereby stabilizing the surface of carbon black as well as that of high voltage cathode material.

  8. 有机电解液型锂空气电池空气电极研究进展%Research progress on air electrode in organic electrolyte lithium-air battery

    Institute of Scientific and Technical Information of China (English)

    罗仲宽; 尹春丽; 吴其兴; 王芳; 黄洋; 李豪君; 魏蒙蒙

    2015-01-01

    Due to the advantages of ultra-high energy density, lithium-air batteries based on organic electrolyte system have received widespread concern. To seek after a high-performance, safety and applicable lithium-air battery, a lot of scholars have conducted numerous research works on cathode materials, catalysts, electrolyte, and lithium cathode. Air electrode optimization and electrolyte stability are the keys to obtaining high performance lithium-air batteries. We review some of the latest research progress on air electrode reaction mechanisms, influence factors of air electrode, materials for air cathode and catalysts in organic electrolyte lithium-air batteries. Meanwhile, advantages and disadvantages of all kinds of porous materials and catalysts, as well as impact on the electrochemical performance of batteries, were analysed. Based on these studies, we put forward the future direction for air electrodes of lithium-air batteries is to build a unique porous electrode structure with new composite oxide catalysts, to achieve high-capacity, long-life lithium-air batteries.%有机电解液体系的锂空气电池因其超高能量密度受到广泛关注。为寻求高性能、安全实用的锂空气电池,国内外就正极材料、催化剂、电解液和锂负极等开展了大量研究,其中空气电极的优化、电解液的稳定性是锂空气电池高性能发挥的关键。介绍了近年有机电解液锂空气电池空气电极上的反应机理、空气电极影响因素、正极材料和催化剂等最新研究进展,分析了各类多孔材料和催化剂的优缺点,及其对电池电化学性能的影响,结合本课题组研究成果,指出了锂空气电池空气电极的发展方向,即结合新型复合氧化物催化剂,构筑独特的多孔电极结构,以实现高容量、长寿命的锂空气电池。

  9. In-plane vacancy-enabled high-power Si-graphene composite electrode for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Xin; Hayner, Cary M.; Kung, Mayfair C.; Kung, Harold H. [Department of Chemical and Biological Engineering, Northwestern University, Evanston, Illinois, 60208 (United States)

    2011-11-15

    Introducing a high density of in-plane, nanometer-sized carbon vacancies in graphene sheets greatly enhances ion diffusion across the sheets in a Si-graphene composite. The flexible, self-supporting three-dimensional conducting graphenic scaffold incorporating Si nanoparticles exhibit excellent rate performance and tolerance to structural deformation, which represents an attractive high power-high capacity anode material for Li-ion batteries. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  10. Silver decorated LaMnO3 nanorod/graphene composite electrocatalysts as reversible metal-air battery electrodes

    Science.gov (United States)

    Hu, Jie; Liu, Qiunan; Shi, Lina; Shi, Ziwei; Huang, Hao

    2017-04-01

    Perovskite LaMnO3 nanorod/reduced graphene oxides (LMO-NR/RGO) decorated with Ag nanoparticles are studied as a bifunctional catalyst for oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) in alkaline electrolyte. LMO-NR/RGO composites are synthesized by using cetyltrimethyl ammonium bromide (CTAB) as template via a simple hydrothermal reaction followed by heat treatment; overlaying of Ag nanoparticles is obtained through a traditional silver mirror reaction. Electron microscopy reveals that LMO-NR is embedded between the sheets of RGO, and the material is homogeneously overlaid with Ag nanoparticles. The unique composite morphology of Ag/LMO-NR/RGO not only enhances the electron transport property by increasing conductivity but also facilitates the diffusion of electrolytes and oxygen. As confirmed by electrochemical testing, Ag/LMO-NR/RGO exhibits very strong synergy with Ag nanoparticles, LMO-NR, and RGO, and the catalytic activities of Ag/LMO-NR/RGO during ORR and OER are significantly improved. With the novel catalyst, the homemade zinc-air battery can be reversibly charged and discharged and display a stable cycle performance, indicating the great potential of this composite as an efficient bifunctional electrocatalyst for metal-air batteries.

  11. Thermophysical properties of LiCoO₂-LiMn₂O₄ blended electrode materials for Li-ion batteries.

    Science.gov (United States)

    Gotcu, Petronela; Seifert, Hans J

    2016-04-21

    Thermophysical properties of two cathode types for lithium-ion batteries were measured by dependence on temperature. The cathode materials are commercial composite thick films containing LiCoO2 and LiMn2O4 blended active materials, mixed with additives (binder and carbon black) deposited on aluminium current collector foils. The thermal diffusivities of the cathode samples were measured by laser flash analysis up to 673 K. The specific heat data was determined based on measured composite specific heat, aluminium specific heat data and their corresponding measured mass fractions. The composite specific heat data was measured using two differential scanning calorimeters over the temperature range from 298 to 573 K. For a comprehensive understanding of the blended composite thermal behaviour, measurements of the heat capacity of an additional LiMn2O4 sample were performed, and are the first experimental data up to 700 K. Thermal conductivity of each cathode type and their corresponding blended composite layers were estimated from the measured thermal diffusivity, the specific heat capacity and the estimated density based on metallographic methods and structural investigations. Such data are highly relevant for simulation studies of thermal management and thermal runaway in lithium-ion batteries, in which the bulk properties are assumed, as a common approach, to be temperature independent.

  12. The microstructure matters: breaking down the barriers with single crystalline silicon as negative electrode in Li-ion batteries

    Science.gov (United States)

    Sternad, M.; Forster, M.; Wilkening, M.

    2016-08-01

    Silicon-based microelectronics forms a major foundation of our modern society. Small lithium-ion batteries act as the key enablers of its success and have revolutionised portable electronics used in our all everyday’s life. While large-scale LIBs are expected to help establish electric vehicles, on the other end of device size chip-integrated Si-based μ-batteries may revolutionise microelectronics once more. In general, Si is regarded as one of the white hopes since it offers energy densities being ten times higher than conventional anode materials. The use of monocrystalline, wafer-grade Si, however, requires several hurdles to be overcome since it its volume largely expands during lithiation. Here, we will show how 3D patterned Si wafers, prepared by the sophisticated techniques from semiconductor industry, are to be electrochemically activated to overcome these limitations and to leverage their full potential being reflected in stable charge capacities (>1000 mAhg–1) and high Coulomb efficiencies (98.8%).

  13. The microstructure matters: breaking down the barriers with single crystalline silicon as negative electrode in Li-ion batteries.

    Science.gov (United States)

    Sternad, M; Forster, M; Wilkening, M

    2016-08-17

    Silicon-based microelectronics forms a major foundation of our modern society. Small lithium-ion batteries act as the key enablers of its success and have revolutionised portable electronics used in our all everyday's life. While large-scale LIBs are expected to help establish electric vehicles, on the other end of device size chip-integrated Si-based μ-batteries may revolutionise microelectronics once more. In general, Si is regarded as one of the white hopes since it offers energy densities being ten times higher than conventional anode materials. The use of monocrystalline, wafer-grade Si, however, requires several hurdles to be overcome since it its volume largely expands during lithiation. Here, we will show how 3D patterned Si wafers, prepared by the sophisticated techniques from semiconductor industry, are to be electrochemically activated to overcome these limitations and to leverage their full potential being reflected in stable charge capacities (>1000 mAhg(-1)) and high Coulomb efficiencies (98.8%).

  14. Glyoxalated polyacrylamide as a covalently attachable and rapidly cross-linkable binder for Si electrode in lithium ion batteries

    Science.gov (United States)

    Yoo, Jung-Keun; Jeon, Jaebeom; Kang, Kisuk; Jung, Yeon Sik

    2017-01-01

    Recently, investigation of Si-based anode materials for rechargeable battery applications garnered much interest due to its exceptionally high capacity. High-capacity Si anode ( 4,200 mAhg-1) is highly desirable for the replacement of conventional graphite anode (storage applications such as in electric vehicles (EVs) and energy storage systems (ESSs) for renewable energy sources. However, Si-based anodes suffer from poor cycling stability due to their large volumetric changes during repeated Li insertion. Therefore, development of highly efficient binder materials that can suppress the volume change of Si is one of the most essential parts of improving the performance of batteries. We herein demonstrate highly cross-linked polymeric binder (glyoxalated polyacrylamide) with an enhanced mechanical property by applying wet-strengthening chemistry used in paper industry. We found that the degree of cross-linking can be systematically adjusted by controlling the acidity of the slurry and has a profound effect on the cell performance using Si anode. The enhanced cycle performance of Si nanoparticles obtained by treating the binder at pH 4 can be explained by its strong interaction between the binder and Si surface and current collector, and also rigidity of binder by cross-linking. [Figure not available: see fulltext.

  15. High-rate and ultralong cycle-life LiFePO4 nanocrystals coated by boron-doped carbon as positive electrode for lithium-ion batteries

    Science.gov (United States)

    Feng, Jinpeng; Wang, Youlan

    2016-12-01

    An evolutionary modification approach, boron-doped carbon coating, has been used to improve the electrochemical performances of positive electrodes for lithium-ion batteries, and demonstrates apparent and significant modification effects. In this study, the boron-doped carbon coating is firstly adopted and used to decorate the performance of LiFePO4. The obtained composite exhibits a unique core-shell structure with an average diameter of 140 nm and a 4 nm thick boron-doped carbon shell that uniformly encapsulates the core. Owing to the boron element which could induce high amount of defects in the carbon, the electronic conductivity of LiFePO4 is greatly ameliorated. Thus, the boron-doped composite shows superior rate capability and cycle stability than the undoped sample. For instance, the reversible specific capacity of LiFePO4@B0.4-C can reach 164.1 mAh g-1 at 0.1C, which is approximately 96.5% of the theoretical capacity (170 mAh g-1). Even at high rate of 10C, it still shows a high specific capacity of 126.8 mAh g-1 and can be maintained at 124.5 mAh g-1 after 100 cycles with capacity retention ratio of about 98.2%. This outstanding Li-storage property enable the present design strategy to open up the possibility of fabricating the LiFePO4@B-C composite for high-performance lithium-ion batteries.

  16. Production of Sn–Cu/MWCNT composite electrodes for Li-ion batteries by using electroless tin coating

    Energy Technology Data Exchange (ETDEWEB)

    Uysal, Mehmet, E-mail: mehmetu@sakarya.edu.tr; Cetinkaya, Tugrul; Kartal, Muhammet, E-mail: kartal@sakarya.edu.tr; Alp, Ahmet; Akbulut, Hatem

    2014-12-01

    Cycling stability of pure tin electrodes were aimed to improve by using a suitable combination of copper and multiwalled carbon nanotubes (MWCNTs). For this purpose, firstly Sn–Cu composite powders were produced using an electroless process. Then, Sn–Cu/MWCNT composite electrodes were prepared with dispersing different amounts of MWCNT (10 wt.%, 20 wt.%, 40 wt.%) by high energy mechanical milling method. The surface morphology of the produced Sn–Cu/MWCNT composite powders was characterized using scanning electron microscopy (SEM), and energy dispersive spectroscopy (EDS) was used to determine the elemental surface composition of the composites. X-ray diffraction (XRD) analysis was performed to investigate the structure of the Sn–Cu/MWCNT composite powders. The electrochemical performance of Sn–Cu/MWCNT composite electrodes has been investigated by charge/discharge tests and cyclic voltammetry experiments. The cell discharge capacities were determined at a constant current in voltage range between 0.02 V and 1.5 V. AC Electrochemical Impedance Spectroscopy (EIS) analysis was also carried out to measure resistivity and Li-diffusion in the assembled cells. The amounts of MWCNTs were shown to be a crucial factor to improve Sn–Cu/MWCNT composite anodes for cyclability and reversible capacity. - Highlights: • Sn–Cu/MWCNT anodes were produced by high energy mechanical milling and electroless method. • MWCNT increases electronic contact between current collector and active material. • The discharge capacity of Sn–Cu/40MWCNT composite was found to be 439 mAh g{sup −1} even after 30 cycles.

  17. Accelerating rate calorimetry studies of the reactions between ionic liquids and charged lithium ion battery electrode materials

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Yadong; Dahn, J.R. [Department of Physics and Atmospheric Science, Dalhousie University, Halifax, NS (Canada); Zaghib, K.; Guerfi, A. [Institut de Recherche d' Hydro-Quebec, 1800 Lionel-Boulet, Varennes, Que. (Canada); Bazito, Fernanda F.C.; Torresi, Roberto M. [Instituto de Quimica Universidade de Sao Paulo, CP 26077, 05513-970 Sao Paulo (Brazil)

    2007-06-30

    Using accelerating rate calorimetry (ARC), the reactivity between six ionic liquids (with and without added LiPF{sub 6}) and charged electrode materials is compared to the reactivity of standard carbonate-based solvents and electrolytes with the same electrode materials. The charged electrode materials used were Li{sub 1}Si, Li{sub 7}Ti{sub 4}O{sub 12} and Li{sub 0.45}CoO{sub 2}. The experiments showed that not all ionic liquids are safer than conventional electrolytes/solvents. Of the six ionic liquids tested, 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMI-FSI) shows the worst safety properties, and is much worse than conventional electrolyte. 1-Ethyl-3-methylimidazolium bis(trifluoromethanesulfonyl)imide (EMI-TFSI) and 1-propyl-1-methylpyrrolidinium bis(fluorosulfonyl)imide (Py13-FSI) show similar reactivity to carbonate-based electrolyte. The three ionic liquids 1-butyl-2,3-dimethylimidazolium bis(trifluoromethanesulfonyl)imide (BMMI-TFSI), 1-butyl-1-methylpiperidinium bis(trifluoromethanesulfonyl)imide (Pp14-TFSI) and N-trimethyl-N-butylammonium bis(trifluoromethanesulfonyl)imide (TMBA-TFSI) show similar reactivity and are much safer than the conventional carbonate-based electrolyte. A comparison of the reactivity of ionic liquids with common anions and cations shows that ionic liquids with TFSI{sup -} are safer than those with FSI{sup -}, and liquids with EMI{sup +} are worse than those with BMMI{sup +}, Py13{sup +}, Pp14{sup +} and TMBA{sup +}. (author)

  18. X-ray absorption near-edge structure study on positive electrodes of degraded lithium-ion battery

    Science.gov (United States)

    Shikano, Masahiro; Kobayashi, Hironori; Koike, Shinji; Sakaebe, Hikari; Saito, Yoshiyasu; Hori, Hironobu; Kageyama, Hiroyuki; Tatsumi, Kuniaki

    18650-type cylindrical cells using LiNi 1/3Mn 1/3Co 1/3O 2 (NMC) and hard carbon as positive and negative electrode material, respectively, were fabricated and degraded by cycle tests. The capacity of the cells remained more than 95% and 85% after cycle tests at 25 and 50 °C, respectively. After the cycle tests, Li-deficient cubic phase was observed on the surface of NMC. This phenomenon should be related to the degradation mechanism of this type of cell.

  19. Metal Foam as Positive Electrode Current Collector for LiFePO4-Based Li-Ion Battery

    Science.gov (United States)

    Yang, Gui Fu; Song, Jae Sun; Kim, Hyung Yoon; Joo, Seung Ki

    2013-10-01

    In order to improve the kinetic performance of LiFePO4-based Li-ion batteries, three dimensional metal foams were used as positive current collector. In the case of conventional Ni foam, the organic electrolyte of the cell was decomposed with the ionization of Ni during charge and discharge. The low tolerance of Ni was solved by using NiCrAl foam which was manufactured by alloying NiCrAl powder with Ni foam. From the electrochemical analysis, it shows that the kinetic performance of the cell by using a three dimensional NiCrAl foam was much superior to that in the case of conventional foil type.

  20. Electrolytes for advanced batteries

    Energy Technology Data Exchange (ETDEWEB)

    Blomgren, G.E. [Energizer, Westlake, OH (United States)

    1999-09-01

    The choices of the components of the electrolyte phase for advanced batteries (lithium and lithium ion batteries) are very sensitive to the electrodes which are used. There are also a number of other requirements for the electrolyte phase, which depend on the cell design and the materials chosen for the battery. The difficulty of choice is compounded when the cell is a rechargeable one. This paper looks at each of these requirements and the degree to which they are met for lithium and lithium ion batteries. The discussion is broken into sections on anode or negative electrode stability requirements, cathode or positive electrode stability requirements, conductivity needs, viscosity and wetting requirements. The effects of these properties and interactions on the performance of batteries are also discussed. (orig.)

  1. Performance comparisons and resistance modeling for multi-segment electrode designs of power-oriented lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Y.-S. [Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 621, Taiwan (China); Chang, K.-H. [Department of Chemical Engineering, National Tsing Hua University, Hsin-Chu 30013, Taiwan (China); Department of Chemical Engineering, National Chung Cheng University, Chia-Yi 621, Taiwan (China); Hu, C.-C., E-mail: cchu@che.nthu.edu.t [Department of Chemical Engineering, National Tsing Hua University, Hsin-Chu 30013, Taiwan (China); Cheng, T.-T. [E-ONE MOLI ENERGY CORP, Southern Taiwan Science Park, No. 10, Dali 2nd Rd., Shanhua, Tainan 74144, Taiwan (China)

    2010-09-01

    This study investigates the influence of tab position and quantity as well as multi-segment electrodes in cell design for the performance of an 18650 power-oriented lithium-ion cell. The resistances of cells with traditional and center-tab designs are simulated by a simplified model. It shows that tab position significantly influences the cell resistance even when other components in the cell are fixed. The performances of both center-tab and traditional designs are compared by the cell direct-current resistance (DCR), body temperature, and 15 A cycling test to demonstrate the impact of cell design. The multi-tab design also shows better performance than the single-tab design for power cells; however there are diminishing returns for cells with three or more tabs as the additional tabs do not significantly reduce the cell resistance. The two-tab design is concluded to be the best choice for an 18650 power cell considering the process ability and overall high-rate performance. The difference in the waste power between the center-tab and the traditional designs, which is transformed into heat, is the main reason for the poor high-rate cycling performance as expected. Such modeling provides a quick design reference for a power cell with new size to get the most suitable electrode design.

  2. A desalination battery.

    Science.gov (United States)

    Pasta, Mauro; Wessells, Colin D; Cui, Yi; La Mantia, Fabio

    2012-02-08

    Water desalination is an important approach to provide fresh water around the world, although its high energy consumption, and thus high cost, call for new, efficient technology. Here, we demonstrate the novel concept of a "desalination battery", which operates by performing cycles in reverse on our previously reported mixing entropy battery. Rather than generating electricity from salinity differences, as in mixing entropy batteries, desalination batteries use an electrical energy input to extract sodium and chloride ions from seawater and to generate fresh water. The desalination battery is comprised by a Na(2-x)Mn(5)O(10) nanorod positive electrode and Ag/AgCl negative electrode. Here, we demonstrate an energy consumption of 0.29 Wh l(-1) for the removal of 25% salt using this novel desalination battery, which is promising when compared to reverse osmosis (~ 0.2 Wh l(-1)), the most efficient technique presently available.

  3. A Desalination Battery

    KAUST Repository

    Pasta, Mauro

    2012-02-08

    Water desalination is an important approach to provide fresh water around the world, although its high energy consumption, and thus high cost, call for new, efficient technology. Here, we demonstrate the novel concept of a "desalination battery", which operates by performing cycles in reverse on our previously reported mixing entropy battery. Rather than generating electricity from salinity differences, as in mixing entropy batteries, desalination batteries use an electrical energy input to extract sodium and chloride ions from seawater and to generate fresh water. The desalination battery is comprised by a Na 2-xMn 5O 10 nanorod positive electrode and Ag/AgCl negative electrode. Here, we demonstrate an energy consumption of 0.29 Wh l -1 for the removal of 25% salt using this novel desalination battery, which is promising when compared to reverse osmosis (∼ 0.2 Wh l -1), the most efficient technique presently available. © 2012 American Chemical Society.

  4. Flame treatment of graphene oxides: cost-effective production of nanoporous graphene electrode for Lithium-ion batteries

    Science.gov (United States)

    Jiang, Hao-Bo; Zhang, Yong-Lai; Zhang, Yi; Liu, Yan; Fu, Xiu-Yan; Liu, Yu-Qing; Wang, Chun-Dong; Sun, Hong-Bo

    2015-12-01

    A facile production of highly porous graphene foam by using flame treatment of graphene oxide (GO) is proposed. Highly porous architectures with randomly distributed micro-crack and micro-slit were produced due to the high temperature induced ruinous reduction and rapid expansion of GO. Synchronously, abundant oxygen-containing groups (OCGs) on GO sheets could be effectively removed after flame treatment, which renders significantly increased conductivity to the resultant flame reduced GO (FR-GO). The synergistic effect of micro/nanostructuring and the OCGs removal makes FR-GO a promising candidate for electrode materials. Compared with chemically reduced GO (CR-GO), FR-GO delivers much higher specific capacity. It gives us some hints that flame treatment of graphene-based material is a smart strategy for cost-effective production of anode materials for commercial application.

  5. The mechanism of the sodiation and desodiation in Super P carbon electrode for sodium-ion battery

    Science.gov (United States)

    Wu, Chun-Ming; Pan, Ping-I.; Cheng, Yin-Wei; Liu, Chuan-Pu; Chang, Chia-Chin; Avdeev, Maxim; Lin, Shih-kang

    2017-02-01

    The sodiation and desodiation of sodium (Na) into the Super-P carbon anode material were investigated using electrochemical analyses, high-resolution transmission electron microscopy (HRTEM), and neutron powder diffraction (NPD). In the sodiated Super-P carbon, sodium is stored both in the graphite interlayer space of carbon nano-particles and pores between the particles. Sodium metal clusters found in micro-pores between the carbon particles are responsible for the large irreversible capacity of the Super-P electrode. The graphite interlayer distance increases on sodiation from 3.57 Å to two distinct values of ∼3.84 and 4.41 Å. The mechanism of the process is discussed.

  6. Hybrid nanostructured microporous carbon-mesoporous carbon doped titanium dioxide/sulfur composite positive electrode materials for rechargeable lithium-sulfur batteries

    Science.gov (United States)

    Zegeye, Tilahun Awoke; Kuo, Chung-Feng Jeffrey; Wotango, Aselefech Sorsa; Pan, Chun-Jern; Chen, Hung-Ming; Haregewoin, Atetegeb Meazah; Cheng, Ju-Hsiang; Su, Wei-Nien; Hwang, Bing-Joe

    2016-08-01

    Herein, we design hybrid nanostructured microporous carbon-mesoporous carbon doped titanium dioxide/sulfur composite (MC-Meso C-doped TiO2/S) as a positive electrode material for lithium-sulfur batteries. The hybrid MC-Meso C-doped TiO2 host material is produced by a low-cost, hydrothermal and annealing process. The resulting conductive material shows dual microporous and mesoporous behavior which enhances the effective trapping of sulfur and polysulfides. The hybrid MC-Meso C-doped TiO2/S composite material possesses rutile TiO2 nanotube structure with successful carbon doping while sulfur is uniformly distributed in the hybrid MC-Meso C-doped TiO2 composite materials after the melt-infusion process. The electrochemical measurement of the hybrid material also shows improved cycle stability and rate performance with high sulfur loading (61.04%). The material delivers an initial discharge capacity of 802 mAh g-1 and maintains it at 578 mAh g-1 with a columbic efficiency greater than 97.1% after 140 cycles at 0.1 C. This improvement is thought to be attributed to the unique hybrid nanostructure of the MC-Meso C-doped TiO2 host and the good dispersion of sulfur in the narrow pores of the MC spheres and the mesoporous C-doped TiO2 support.

  7. Morphology-Tuned Synthesis of NiCo2 O4 -Coated 3D Graphene Architectures Used as Binder-Free Electrodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Zhang, Chunfei; Yu, Jong-Sung

    2016-03-18

    Nanostructured NiCo2O4 is directly grown on the surface of three-dimensional graphene-coated nickel foam (3D-GNF) by a facile electrodeposition technique and subsequent annealing. The resulting NiCo2O4 possesses a distinct flower or sheet morphology, tuned by potential or current variation electrodeposition, which are used as binder-free lithium-ion battery anodes for the first time. Both samples exhibit high lithium storage capacity, profiting from the unique binder-free electrode structures. The flower-type NiCo2O4 demonstrates high reversible discharge capacity (1459 mAh g(-1) at 200 mA g(-1)) and excellent cyclability with around 71% retention of the reversible capacity after 60 cycles, which are superior to the sheet-type NiCo2O4. Such superb performance can be attributed to high volume utilization efficiency with unique morphological character, a well-preserved connection between the active materials and the current collector, a short lithium-ion diffusion path, and fast electrolyte transfer in the binder-free NiCo2O4 coated 3D graphene structure. The simple preparation process and easily controllable morphology make the binder-free NiCo2O4/3D-GNF hybrid a potential material for commercial applications.

  8. Ion-exchange synthesis and improved Li insertion property of lithiated H2Ti12O25 as a negative electrode material for lithium-ion batteries

    Directory of Open Access Journals (Sweden)

    Kunimitsu Kataoka

    2016-03-01

    Full Text Available We successfully prepared the lithiated H2Ti12O25 sample by the H+/Li+ ion exchange synthetic technique in the molten LiNO3 at 270 °C using H2Ti12O25 as a starting compound. Chemical composition of the obtained lithiated H2Ti12O25 sample was determined to be H1.05Li0.35Ti12O25-δ having δ = 0.3 by ICP-AES and DTA-TG analyses. The H+/Li+ ion exchange was also confirmed by powder XRD, 1H-MAS NMR, and 7Li-MAS NMR measurements. Electrochemical Li insertion and extraction measurements revealed that the initial coulombic efficiency was improved from 88% in H2Ti12O25 to 93% in the lithiated H2Ti12O25 sample. In addition, superior capacity retention properties for the charge and discharge cycling performance and good charge rate capability of the present lithiated H2Ti12O25 were confirmed in the electrochemical measurements. Accordingly, the lithiated H2Ti12O25 is suggested to be one of the promising high-voltage and high-capacity oxide negative electrodes in advanced lithium-ion batteries.

  9. Synthesis and Characterization of Stable and Binder-Free Electrodes of TiO2 Nanofibers for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Phontip Tammawat

    2013-01-01

    Full Text Available An electrospinning technique was used to fabricate TiO2 nanofibers for use as binder-free electrodes for lithium-ion batteries. The as-electrospun nanofibers were calcined at 400–1,000°C and characterized using X-ray diffraction (XRD, scanning electron microscopy (SEM, and transmission electron microscopy (TEM. SEM and TEM images showed that the fibers have an average diameter of ~100 nm and are composed of nanocrystallites and grains, which grow in size as the calcination temperature increases. The electrochemical properties of the nanofibers were evaluated using galvanostatic cycling and electrochemical impedance spectroscopy. The TiO2 nanofibers calcined at 400°C showed higher electronic conductivity, higher discharge capacity, and better cycling performance than the nanofibers calcined at 600, 800, and 1,000°C. The TiO2 nanofibers calcined at 400°C delivered an initial reversible capacity of 325 mAh·g−1 approaching their theoretical value at 0.1 C rate and over 175 mAh·g−1 at 0.3 C rate with limited capacity fading and Coulombic efficiency between 96 and 100%.

  10. Peapod-like V2O3 nanorods encapsulated into carbon as binder-free and flexible electrodes in lithium-ion batteries

    Science.gov (United States)

    Li, Xingxing; Fu, Jijiang; Pan, Zhiguo; Su, Jianjun; Xu, Jiangwen; Gao, Biao; Peng, Xiang; Wang, Lei; Zhang, Xuming; Chu, Paul K.

    2016-11-01

    Designing and fabricating electrodes with excellent mechanical flexibility and superior electrochemical performance for high-performance lithium ion battery (LIBs) is challenging. Herein, ultralong peapod-like nanowires (NWs) composed of short vanadium sesquioxide nanorods (V2O3 NRs) encapsulated with carbon are produced as high-performance anode materials. The freestanding and flexible film has a high capacity of 210 mAh g-1 at a current density of 0.1 C, and exhibits appreciable rate capability with 68% capacitance retention when the current density is increased from 0.1 to 1 C, and excellent long-term cycling stability without apparent capacity fading after 125 cycles, which is better then that of the active carbon mixed V2O3 NRs and bare V2O3 NRs. The outstanding electrochemical performance is attributed to proper accommodation of the volume expansion of the vanadium oxide in the carbon in the lithiation/delithiation process as well as the outer conductive three-dimensional (3D) carbon network. The formation mechanism of the peapod-like structure is investigated by thermogravimetric analysis connected to a mass spectrometer (MS). The ultralong peapod-like nanostructure overcomes the physical and chemical drawbacks of vanadium oxide and has large potential applicability for flexible energy-storage devices.

  11. Multi-Electrode Resistivity Probe for Investigation of Local Temperature Inside Metal Shell Battery Cells via Resistivity: Experiments and Evaluation of Electrical Resistance Tomography

    Directory of Open Access Journals (Sweden)

    Xiaobin Hong

    2015-01-01

    Full Text Available Direct Current (DC electrical resistivity is a material property that is sensitive to temperature changes. In this paper, the relationship between resistivity and local temperature inside steel shell battery cells (two commercial 10 Ah and 4.5 Ah lithium-ion cells is innovatively studied by Electrical Resistance Tomography (ERT. The Schlumberger configuration in ERT is applied to divide the cell body into several blocks distributed in different levels, where the apparent resistivities are measured by multi-electrode surface probes. The investigated temperature ranges from −20 to 80 °C. Experimental results have shown that the resistivities mainly depend on temperature changes in each block of the two cells used and the function of the resistivity and temperature can be fitted to the ERT-measurement results in the logistical-plot. Subsequently, the dependence of resistivity on the state of charge (SOC is investigated, and the SOC range of 70%–100% has a remarkable impact on the resistivity at low temperatures. The proposed approach under a thermal cool down regime is demonstrated to monitor the local transient temperature.

  12. Progress on electrode materials for lead acid flow battery based on electrolyte with soluble lead%全沉积型铅酸液流电池电极材料研究进展

    Institute of Scientific and Technical Information of China (English)

    刘旭东; 毕孝国; 牛微

    2012-01-01

    A novel lead acid flow battery with no separator and a single electrolyte, lead (II) in organic acid, was described. The function and performance requirements of the electrode of lead acid flow battery were summed. The progress and recent development of the study on the electrode materials were reviewed. The results suggest that the most prospective electrode materials are the graphite felt and carbon foam and the study on the electrode modification is very important.%全沉积型铅酸液流电池是以可溶性二价铅离子在有机酸中的电沉积/溶解反应为充放电基础的新型储能装置.归纳了全沉积型铅酸液流电池电极的功能和性能要求,介绍了电极材料的研究进展情况.分析得到了当前最具应用前景的电极材料是碳素类和泡沫材料类,尤其是石墨毡和碳泡沫电极表面的改性研究是液流电池的一个重要研究方向.

  13. 正极配方设计对锂离子电池寿命的影响研究%Influence of cathode electrode formula design on cycle life performance of LiFePO4 battery

    Institute of Scientific and Technical Information of China (English)

    吴静; 王炜娜; 李锦

    2013-01-01

    The resistivity and infiltration of electrode plate was researched through four-probe method and other analytical method,and the positive electrode formula was optimized.The result show that type A LiFePO4 material and 18650 batteries which adopted type A material exhibit more excellent performance.The addition of VGCF to original high compact electrode formula improves the conductivity and infiltration of electrode plate,and enhances cycle life of the high specific energy battery.%通过采用四探针等手段对极片的电阻率、浸润性等进行了研究分析,并对高比能量电池的正极配方进行了优化.测试结果显示:A型号磷酸铁锂材料及其所制备的18650试验电池性能更为优越,特选取A作为高比能量电池正极活性物质;在原有高压实极片电极配方基础上添加了一定量的导电碳纤维,提高了极片的电导率及浸润性,进而提高了高比能电池的循环寿命.

  14. Alloys of clathrate allotropes for rechargeable batteries

    Science.gov (United States)

    Chan, Candace K; Miller, Michael A; Chan, Kwai S

    2014-12-09

    The present disclosure is directed at an electrode for a battery wherein the electrode comprises clathrate alloys of silicon, germanium or tin. In method form, the present disclosure is directed at methods of forming clathrate alloys of silicon, germanium or tin which methods lead to the formation of empty cage structures suitable for use as electrodes in rechargeable type batteries.

  15. Batteries: Imaging degradation

    Science.gov (United States)

    Shearing, Paul R.

    2016-11-01

    The degradation and failure of Li-ion batteries is strongly associated with electrode microstructure change upon (de)lithiation. Now, an operando X-ray tomography approach is shown to correlate changes in the microstructure of electrodes to cell performance, and thereby predict degradation pathways.

  16. Research of new AB type hydrogen storage materials that can be used as a negative electrode in nickel -metal hydride battery; Recherche de nouveaux composes intermetalliques hydrurables de type AB utilisables comme electrode negative d`accumulateur nickel-hydrure

    Energy Technology Data Exchange (ETDEWEB)

    Jordy, Ch.

    1994-12-15

    The aim of this work is to determine new AB type hydrogen storage materials that can be used as a negative electrode in nickel-metal hydride battery. The main requested solid-gas hydrogenation properties are as follows : a reversible capacity higher than 400 mAh/g and a plateau pressure close to 0, 01 MPa at 25 deg C. Binary intermetallic compounds have been selected according to their high hydrogen capacity. The thermodynamic properties of the hydride have to be adjusted by partial substitution of the A and/or B elements. The selected binary intermetallic rate to the substitution was based on known thermodynamic models and on criteria on hydrogen atom occupation in interstitial sites. The only alloys, which could have interest, are the one which are homogeneous. Amongst them, the compounds Ti(Fe{sub 1-x}) where M=Ni,Co,Mn,Cr, showed a solid-gas capacity higher than 400 mAh/g and a plateau pressure close to 0,01 MPa at 25 deg C. Nevertheless, the electrochemical capacity is extremely low due to the iron corrosion in concentrated KOH. The electrochemical capacities of (Ti{sub 1-x-y} Zr{sub x}M{sub y})Ni compounds for M=V and Si are the most promising in the AB type since a 350 m Ah/g reversible capacity has been measured bY THE CONSTANT POTENTIAL METHOD. We also showed that the partial zirconium substitution made the martensitic transformation temperature higher. (author)

  17. Intrinsic thermodynamic and kinetic properties of Sb electrodes for Li-ion and Na-ion batteries: Experiment and Theory

    Energy Technology Data Exchange (ETDEWEB)

    Baggetto, Loic [ORNL; Ganesh, Panchapakesan [ORNL; Sun, Che Nan [ORNL; Meisner, Roberta Ann [ORNL; Zawodzinski, Thomas A [ORNL; Veith, Gabriel M [ORNL

    2013-01-01

    energy barrier for near-neighbor vacancy motion, predominant in these close-packed phases is about twice for Na than for Li. Our analysis tries to relate the lower intrinsic diffusivity of Na compared to Li with the long-range strain propagation induced by the former, thereby leading to an intrinsic origin of differences in rates, mechanical properties and amorphization. Finally, the surface chemistry of Sb electrodes cycled in NaClO4 dissolved in pure PC with(out) the addition of 5wt% EC or FEC shows presence of ethers and NaF for the EC- and FEC-based electrolytes, respectively, and SEI films rich in Na-based carbonates.

  18. Studies on performance and electrode materials for vanadium flow battery%全钒液流电池性能及电极材料研究

    Institute of Scientific and Technical Information of China (English)

    杜涛; 廖小东; 郝彰翔; 李爱魁; 滕隽

    2013-01-01

    The performance of graphite felt before and after the activation were compared, and the electrochemical performance of vanadium flow battery was studied by the charging and discharging instrument with the graphite felt after activation as electrode. The constant current charging and discharging experiments show that the activation of graphite felt can be increased by sulfuric acid. The energy efficiency deceases with the higher charging-discharging current, and the maximal energy efficiency achieve 75.2%; the columb efficiency increases with the higher charging-discharging current and the maximal efficiency can achieve 95.01%. The internal communication decreases with the higher SOC.%进行了石墨毡活化前后的性能比较,利用充放电仪器研究了经浓硫酸活化的聚丙烯腈基石墨毡作为电极的全钒液流电池的电化学性能.结果表明:(1)对石墨毡进行浓硫酸活化可增强其化学活性;(2)电池的库仑效率随着充放电电流的增加先增大后减小,最高可达95,01%;(3)电池的能量效率随着充放电电流的增加而减小,最高可达75.20%;(4)电池的交流内阻随电池SOC增加而减小.

  19. Nanostructuring effect of multi-walled carbon nanotubes on electrochemical properties of carbon foam as constructive electrode for lead acid battery

    Science.gov (United States)

    Kumar, Rajeev; Kumari, Saroj; Mathur, Rakesh B.; Dhakate, Sanjay R.

    2015-01-01

    In the present study, nanostructuring effect of multi-walled carbon nanotubes (MWCNTs) on electrochemical properties of coal tar pitch (CTP) based carbon foam (CFoam) was investigated. The different weight fractions of MWCNTs were mixed with CTP and foam was developed from the mixture of CTP and MWCNTs by sacrificial template technique and heat treated at 1,400 and 2,500 °C in inert atmosphere. These foams were characterized by scanning electron microscopy, X-ray diffraction, and potentiostat PARSTAT for cyclic voltammetry. It was observed that, bulk density of CFoam increases with increasing MWCNTs content and decreases after certain amount. The MWCNTs influence the morphology of CFoam and increase the width of ligaments as well as surface area. During the heat treatment, stresses exerting at MWCNTs/carbon interface accelerate ordering of the graphene layer which have positive effect on the electrochemical properties of CFoam. The current density increases from 475 to 675 mA/cm2 of 1,400 °C heat treated and 95 to 210 mA/cm2 of 2,500 °C heat-treated CFoam with 1 wt% MWCNTs. The specific capacitance was decreases with increasing the scan rate from 100 to 1,000 mV/s. In case of 1 % MWCNTs content CFoam the specific capacitance at the scan rate 100 mV/s was increased from 850 to 1,250 μF/cm2 and 48 to 340 μF/cm2 of CFoam heat treated at 1,400 °C and 2,500 °C respectively. Thus, the higher value surface area and current density of MWCNTs-incorporated CFoam heat treated to 1,400 °C can be suitable for lead acid battery electrode with improved charging capability.

  20. The influence of cycling temperature and cycling rate on the phase specific degradation of a positive electrode in lithium ion batteries: A post mortem analysis

    Science.gov (United States)

    Darma, Mariyam Susana Dewi; Lang, Michael; Kleiner, Karin; Mereacre, Liuda; Liebau, Verena; Fauth, Francois; Bergfeldt, Thomas; Ehrenberg, Helmut

    2016-09-01

    The influence of cycling temperatures and cycling rates on the cycling stability of the positive electrode (cathode) of commercial batteries are investigated. The cathode is a mixture of LiMn2O4 (LMO), LiNi0.5Co0.2Mn0.3O2 (NCM) and LiNi0.8Co0.15Al0.05O2 (NCA). It is found that increasing the cycling temperature from 25 °C to 40 °C is detrimental to the long term cycling stability of the cathode. Contrastingly, the improved cycling stability is observed for the cathodes cycled at higher charge/discharge rate (2C/3C instead of 1C/2C). The microstructure analysis by X-ray powder diffraction reveals that a significant capacity fading and an increased overvoltage is observed for NCM and NCA in all the fatigued cathodes. After high number of cycling (above 1500 cycles), NCM becomes partially inactive. In contrast to NCM and NCA, LMO shows a good cycling stability at 25 °C. A pronounced degradation of LMO is only observed for the fatigued cathodes cycled at 40 °C. The huge capacity losses of NCM and NCA are most likely because the blended cathodes were cycled up to 4.12 V vs. the graphite anode during the cycle-life test (corresponds to 4.16 V vs. Li+/Li); which is beyond the stability limit of the layered oxides below 4.05 V vs. Li+/Li.

  1. Electrode for a lithium cell

    Science.gov (United States)

    Thackeray, Michael M.; Vaughey, John T.; Dees, Dennis W.

    2008-10-14

    This invention relates to a positive electrode for an electrochemical cell or battery, and to an electrochemical cell or battery; the invention relates more specifically to a positive electrode for a non-aqueous lithium cell or battery when the electrode is used therein. The positive electrode includes a composite metal oxide containing AgV.sub.3O.sub.8 as one component and one or more other components consisting of LiV.sub.3O.sub.8, Ag.sub.2V.sub.4O.sub.11, MnO.sub.2, CF.sub.x, AgF or Ag.sub.2O to increase the energy density of the cell, optionally in the presence of silver powder and/or silver foil to assist in current collection at the electrode and to improve the power capability of the cell or battery.

  2. The Li-Se battery and its C/Se composite electrode:Opportunities and challenges%锂硒电池及碳/硒电极:机遇与挑战

    Institute of Scientific and Technical Information of China (English)

    李静; 张辰; 陶莹; 凌国维; 杨全红

    2016-01-01

    硒是硫的同族元素,具有较高的电导率、与硫相当的体积比容量,是一种新型锂离子电池正极材料。然而锂硒电池在充放电过程中存在的穿梭效应较大地影响了锂硒电池的电化学性能。目前已有一些关于抑制锂硒电池穿梭效应、提升锂硒电池电化学性能的研究。本文综述了锂硒电池的研究现状,着重介绍了硒碳复合电极的进展,论述了其主要优势及存在的问题,并展望了石墨烯在锂硒电池中的应用,最后对提升锂硒电池电化学性能的关键因素进行了分析。%Selenium is a novel and promising cathode material in lithium ion batteries owing to its high electronic conductivity and a theoretical volumetric capacity comparable to that of S. As a congener of sulfur ( S) , Se has a similar lithiation mechanism to S in charge/discharge when used as the cathode material of a Li-Se battery. However, similar to the Li-S battery, the Li-Se battery suf-fers from a shuttle effect that leads to poor cycle performance and low Coulombic efficiency. This review summarizes recent devel-opments, highlights the excellent performance of Li-Se batteries and focuses on improvements to the carbon/Se composite electrode. The main obstacles are also discussed. The use of porous carbons, especially graphene-based materials, for improving the perform-ance of the Se electrode in high performance Li-Se batteries is highlighted and discussed.

  3. Amorphous LiCoO2sbnd Li2SO4 active materials: Potential positive electrodes for bulk-type all-oxide solid-state lithium batteries with high energy density

    Science.gov (United States)

    Nagao, Kenji; Hayashi, Akitoshi; Deguchi, Minako; Tsukasaki, Hirofumi; Mori, Shigeo; Tatsumisago, Masahiro

    2017-04-01

    Newly amorphous Li2-x/100Cox/100S1-x/100O4-x/50 (xLiCoO2·(100-x)Li2SO4 (mol%)) positive electrode active materials are synthesized using mechanochemical techniques. SEM observation indicates that average radii of the Li1.2Co0.8S0.2O2.4 (80LiCoO2·20Li2SO4 (mol%)) particles are about 3 μm. HR-TEM images indicate that the particles comprise nano-crystalline and amorphous phases. The crystalline phase is attributable to cubic LiCoO2 phase. These active materials exhibit a high electronic conductivity of around 10-5-10-1 S cm-1 and an ionic conductivity of around 10-7-10-6 S cm-1 at room temperature. Bulk-type all-oxide solid-state cells (Lisbnd In alloy/Li3BO3-based glass-ceramic electrolyte/amorphous Li2-x/100Cox/100S1-x/100O4-x/50) are fabricated by pressing at room temperature without high temperature sintering. Although the cell with the milled LiCoO2 shows no capacity, the cell using the Li1.2Co0.8S0.2O2.4 electrode with no conductive components (ca. 150 μm thickness) operates as a secondary battery at 100 °C, with an average discharge potential of 3.3 V (vs. Li+/Li) and discharge capacity of 163 mAh g-1. A positive electrode with large amounts of active materials is suitable for achieving high energy density in all-solid-state batteries. These newly synthesized amorphous Li2-x/100Cox/100S1-x/100O4-x/50 electrodes with ionic and electronic conductivities and good processability meet that demand.

  4. Methods on Investigating Properties of Electrode/Electrolyte Interfaces in Lithium-Ion Batteries%锂离子电池电极界面特性研究方法

    Institute of Scientific and Technical Information of China (English)

    秦银平; 庄全超; 史月丽; 江利; 孙智; 孙世刚

    2011-01-01

    The rechargeable lithium-ion battery has been extensively used in mobile communication and portable instruments due to its many advantages, such as high volumetric and gravimetric energy density and low self-discharge rate. In addition, it is the most promising candidate as the power source for (hybrid) electric vehicles and stationary energy storage. The properties of electrode/electrolyte interfaces play an important role in the electrochemical performance of the electrode material and a battery, such as the capacities, irreversible charge "loss", rate capability and cyclability. In present paper, the methods to investigate the properties of electrode/electrolyte interfaces, for example, traditional electrochemical methods, microscopy methods, spectroscopic methods, electrochemical quartz crystal microgravimetry (EQCM) are summarized. The principles, advantages and disadvantages of these methods and their applications in investigating the properties of electrode/electrolyte interfaces, especially the progress in the combination of these methods to investigate the properties of electrode/electrolyte interfaces, are introduced in detail, and these methods will be considerable to study the new materials or the traditional materials for lithium-ion batteries in the future.%电极界面特性是影响锂离子电池充放电循环容量与稳定性的重要因素.本文总结了目前对电极界面特性进行研究的方法,主要包括传统的电化学方法、显微方法、谱学方法、电化学石英微晶天平等,重点论述了上述研究方法的原理、优缺点和在研究电极界面特性中的应用,以及这些方法相结合所取得的一些研究进展,并指出在今后的工作中,无论是对新材料的研究还是传统材料的研究,这些方法都仍将发挥重要作用.

  5. Mesoporous and Nanostructured TiO2 layer with Ultra-High Loading on Nitrogen-Doped Carbon Foams as Flexible and Free-Standing Electrodes for Lithium-Ion Batteries.

    Science.gov (United States)

    Chu, Shiyong; Zhong, Yijun; Cai, Rui; Zhang, Zhaobao; Wei, Shenying; Shao, Zongping

    2016-12-01

    A simple and green method is developed for the preparation of nanostructured TiO2 supported on nitrogen-doped carbon foams (NCFs) as a free-standing and flexible electrode for lithium-ion batteries (LIBs), in which the TiO2 with 2.5-4 times higher loading than the conventional TiO2 -based flexible electrodes acts as the active material. In addition, the NCFs act as a flexible substrate and efficient conductive networks. The nanocrystalline TiO2 with a uniform size of ≈10 nm form a mesoporous layer covering the wall of the carbon foam. When used directly as a flexible electrode in a LIB, a capacity of 188 mA h g(-1) is achieved at a current density of 200 mA g(-1) for a potential window of 1.0-3.0 V, and a specific capacity of 149 mA h g(-1) after 100 cycles at a current density of 1000 mA g(-1) is maintained. The highly conductive NCF and flexible network, the mesoporous structure and nanocrystalline size of the TiO2 phase, the firm adhesion of TiO2 over the wall of the NCFs, the small volume change in the TiO2 during the charge/discharge processes, and the high cut-off potential contribute to the excellent capacity, rate capability, and cycling stability of the TiO2 /NCFs flexible electrode.

  6. Life cycle assessment of sodium-ion batteries

    OpenAIRE

    2016-01-01

    Sodium-ion batteries are emerging as potential alternatives to lithium-ion batteries. This study presents a prospective life cycle assessment for the production of a sodium-ion battery with a layered transition metal oxide as a positive electrode material and hard carbon as a negative electrode material on the battery component level. The complete and transparent inventory data are disclosed, which can easily be used as a basis for future environmental assessments. Na-ion batteries are found ...

  7. LiNi 0.8 Co 0.2 O 2 -based high power lithium-ion battery positive electrodes analyzed by x-ray photoelectron spectroscopy: 2. Following 3 formation cycles

    Energy Technology Data Exchange (ETDEWEB)

    Haasch, Richard T.; Abraham, Daniel A.

    2016-12-01

    High-power lithium-ion batteries are rapidly replacing the nickel metal hydride batteries currently used for energy storage in hybrid electric vehicles. Widespread commercialization of these batteries for vehicular applications is, however, limited by calendar-life performance, thermal abuse characteristics, and cost. The Advanced Technology Development Program was established by the U.S. Department of Energy to address these limitations. An important objective of this program was the development and application of diagnostic tools that provide unique ways to investigate the phenomena that limit lithium-ion cell life, performance, and safety characteristics. This report introduces a set of six Surface Science Spectra xray photoelectron spectroscopy (XPS) comparison records of data collected from positive electrodes (cathode) harvested from cylindrically wound, 18650-type, 1 A h capacity cells. The cathodes included in this study are (1) fresh, (2) following three formation cycles, (3) following calendar-life test for 12 weeks at 40 C, 60% state-of-charge (SOC), (4) following calendar-life test for 8 weeks at 50 C, 60% SOC, (5) following calendar-life test for 8 weeks at 60 C, 60% SOC, and (6) following calendar-life test for 2 weeks at 70 C, 60% SOC.

  8. Introduction to a series of LiNi 0.8 Co 0.2 O 2 -based high-power lithium-ion battery positive electrodes analyzed by x-ray photoelectron spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Haasch, Richard T.; Abraham, Daniel A.

    2016-12-01

    High-power lithium-ion batteries are rapidly replacing the nickel metal hydride batteries currently used for energy storage in hybrid electric vehicles. Widespread commercialization of these batteries for vehicular applications is, however, limited by calendar-life performance, thermal abuse characteristics, and cost. The Advanced Technology Development Program was established by the U.S. Department of Energy to address these limitations. An important objective of this program was the development and application of diagnostic tools that provide unique ways to investigate the phenomena that limit lithium-ion cell life, performance, and safety characteristics. This report introduces a set of six Surface Science Spectra xray photoelectron spectroscopy (XPS) comparison records of data collected from positive electrodes (cathode) harvested from cylindrically wound, 18650-type, 1 A h capacity cells. The cathodes included in this study are (1) fresh, (2) following three formation cycles, (3) following calendar-life test for 12 weeks at 40 C, 60% state-of-charge (SOC), (4) following calendar-life test for 8 weeks at 50 C, 60% SOC, (5) following calendar-life test for 8 weeks at 60 C, 60% SOC, and (6) following calendar-life test for 2 weeks at 70 C, 60% SOC.

  9. Batteries: Overview of Battery Cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Doeff, Marca M

    2010-07-12

    hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and electric vehicles (EVs); a market predicted to be potentially ten times greater than that of consumer electronics. In fact, only Liion batteries can meet the requirements for PHEVs as set by the U.S. Advanced Battery Consortium (USABC), although they still fall slightly short of EV goals. In the case of Li-ion batteries, the trade-off between power and energy shown in Figure 1 is a function both of device design and the electrode materials that are used. Thus, a high power battery (e.g., one intended for an HEV) will not necessarily contain the same electrode materials as one designed for high energy (i.e., for an EV). As is shown in Figure 1, power translates into acceleration, and energy into range, or miles traveled, for vehicular uses. Furthermore, performance, cost, and abuse-tolerance requirements for traction batteries differ considerably from those for consumer electronics batteries. Vehicular applications are particularly sensitive to cost; currently, Li-ion batteries are priced at about $1000/kWh, whereas the USABC goal is $150/kWh. The three most expensive components of a Li-ion battery, no matter what the configuration, are the cathode, the separator, and the electrolyte. Reduction of cost has been one of the primary driving forces for the investigation of new cathode materials to replace expensive LiCoO{sub 2}, particularly for vehicular applications. Another extremely important factor is safety under abuse conditions such as overcharge. This is particularly relevant for the large battery packs intended for vehicular uses, which are designed with multiple cells wired in series arrays. Premature failure of one cell in a string may cause others to go into overcharge during passage of current. These considerations have led to the development of several different types of cathode materials, as will be covered in the next section. Because there is not yet one ideal material that can

  10. Batteries: Overview of Battery Cathodes

    Energy Technology Data Exchange (ETDEWEB)

    Doeff, Marca M

    2010-07-12

    hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and electric vehicles (EVs); a market predicted to be potentially ten times greater than that of consumer electronics. In fact, only Liion batteries can meet the requirements for PHEVs as set by the U.S. Advanced Battery Consortium (USABC), although they still fall slightly short of EV goals. In the case of Li-ion batteries, the trade-off between power and energy shown in Figure 1 is a function both of device design and the electrode materials that are used. Thus, a high power battery (e.g., one intended for an HEV) will not necessarily contain the same electrode materials as one designed for high energy (i.e., for an EV). As is shown in Figure 1, power translates into acceleration, and energy into range, or miles traveled, for vehicular uses. Furthermore, performance, cost, and abuse-tolerance requirements for traction batteries differ considerably from those for consumer electronics batteries. Vehicular applications are particularly sensitive to cost; currently, Li-ion batteries are priced at about $1000/kWh, whereas the USABC goal is $150/kWh. The three most expensive components of a Li-ion battery, no matter what the configuration, are the cathode, the separator, and the electrolyte. Reduction of cost has been one of the primary driving forces for the investigation of new cathode materials to replace expensive LiCoO{sub 2}, particularly for vehicular applications. Another extremely important factor is safety under abuse conditions such as overcharge. This is particularly relevant for the large battery packs intended for vehicular uses, which are designed with multiple cells wired in series arrays. Premature failure of one cell in a string may cause others to go into overcharge during passage of current. These considerations have led to the development of several different types of cathode materials, as will be covered in the next section. Because there is not yet one ideal material that can

  11. Fabrication of 3D core-shell multiwalled carbon nanotube@RuO2 lithium-ion battery electrodes through a RuO2 atomic layer deposition process.

    Science.gov (United States)

    Gregorczyk, Keith E; Kozen, Alexander C; Chen, Xinyi; Schroeder, Marshall A; Noked, Malachi; Cao, Anyuan; Hu, Liangbing; Rubloff, Gary W

    2015-01-27

    Pushing lithium-ion battery (LIB) technology forward to its fundamental scaling limits requires the ability to create designer heterostructured materials and architectures. Atomic layer deposition (ALD) has recently been applied to advanced nanostructured energy storage devices due to the wide range of available materials, angstrom thickness control, and extreme conformality over high aspect ratio nanostructures. A class of materials referred to as conversion electrodes has recently been proposed as high capacity electrodes. RuO2 is considered an ideal conversion material due to its high combined electronic and ionic conductivity and high gravimetric capacity, and as such is an excellent material to explore the behavior of conversion electrodes at nanoscale thicknesses. We report here a fully characterized atomic layer deposition process for RuO2, electrochemical cycling data for ALD RuO2, and the application of the RuO2 to a composite carbon nanotube electrode scaffold with nucleation-controlled RuO2 growth. A growth rate of 0.4 Å/cycle is found between ∼ 210-240 °C. In a planar configuration, the resulting RuO2 films show high first cycle electrochemical capacities of ∼ 1400 mAh/g, but the capacity rapidly degrades with charge/discharge cycling. We also fabricated core/shell MWCNT/RuO2 heterostructured 3D electrodes, which show a 50× increase in the areal capacity over their planar counterparts, with an areal lithium capacity of 1.6 mAh/cm(2).

  12. Direct observation of electronic conductivity transitions and solid electrolyte interphase stability of Na2Ti3O7 electrodes for Na-ion batteries

    Science.gov (United States)

    Zarrabeitia, Maider; Nobili, Francesco; Muñoz-Márquez, Miguel Ángel; Rojo, Teófilo; Casas-Cabanas, Montse

    2016-10-01

    This communication reports the first experimental evidence of an interesting change of transport properties, and particularly of electron conductivity, during the Na+ insertion/extraction process in Na2Ti3O7 negative electrodes. Probed by electrochemical impedance spectroscopy, for 0.0 ≤ x electrochemical cycling and negatively contributes on the capacity fading observed for this electrode material.

  13. Li/Ag2VO2PO4 batteries: the roles of composite electrode constituents on electrochemistry

    Energy Technology Data Exchange (ETDEWEB)

    Bock, David C.; Bruck, Andrea M.; Pelliccione, Christopher J.; Zhang, Yiman; Takeuchi, Kenneth J.; Marschilok, Amy C.; Takeuchi, Esther S. (BNL); (SBU)

    2016-11-01

    Silver vanadium phosphorous oxide, Ag2V2OPO4, was used as a model system to systematically study the impact on the constituents of a composite electrode, including polymeric and conductive additives, on electrochemistry. Three different electrode compositions were investigated.

  14. Carbon and Binder-Free Air Electrodes Composed of Co3O 4 Nanofibers for Li-Air Batteries with Enhanced Cyclic Performance.

    Science.gov (United States)

    Lee, Chan Kyu; Park, Yong Joon

    2015-12-01

    In this study, to fabricate a carbon free (C-free) air electrode, Co3O4 nanofibers were grown directly on a Ni mesh to obtain Co3O4 with a high surface area and good contact with the current collector (the Ni mesh). In Li-air cells, any C present in the air electrode promotes unwanted side reactions. Therefore, the air electrode composed of only Co3O4 nanofibers (i.e., C-free) was expected to suppress these side reactions, such as the decomposition of the electrolyte and formation of Li2CO3, which would in turn enhance the cyclic performance of the cell. As predicted, the Co3O4-nanofiber electrode successfully reduced the accumulation of reaction products during cycling, which was achieved through the suppression of unwanted side reactions. In addition, the cyclic performance of the Li-air cell was superior to that of a standard electrode composed of carbonaceous material.

  15. Air and metal hydride battery

    Energy Technology Data Exchange (ETDEWEB)

    Lampinen, M.; Noponen, T. [Helsinki Univ. of Technology, Otaniemi (Finland). Lab. of Applied Thermodynamics

    1998-12-31

    The main goal of the air and metal hydride battery project was to enhance the performance and manufacturing technology of both electrodes to such a degree that an air-metal hydride battery could become a commercially and technically competitive power source for electric vehicles. By the end of the project it was possible to demonstrate the very first prototype of the air-metal hydride battery at EV scale, achieving all the required design parameters. (orig.)

  16. Progress in electrode materials and electrolyte for aqueous Li-ion battery%水基锂离子电池电极材料及电解液的进展

    Institute of Scientific and Technical Information of China (English)

    尚雨; 金英学; 谭广慧; 邓超

    2013-01-01

    The advantages and mechanism of aqueous Li-ion battery were introduced.The cathode materials for aqueous Li-ion battery such as LiMn2O4,LiCoO2 and LiFe0.5 Mn0.5 PO4/C,the anode materials such as vanadium oxides,activated carbon,polyaniline and the composite membrane coated Li metal were discussed.The preparation method and electrochemical performance of electrode materials were concluded.The electrochemical performance of battery using different electrolytes was summarized.It was pointed out that increasing specific capacity and cycle stability were the development directions of aqueous Li-ion battery.%介绍了水基锂离子电池的优点和原理,探讨了水基锂离子电池中的正极材料:LiMn2 O4、LiCoO2和LiFe0.5 Mn0.5 PO4/C,负极材料:钒的氧化物、活性碳(AC)、聚苯胺(PANI)及复合膜包覆型金属锂.归纳了电极材料的合成方法和电化学性能.综述了使用不同电解液电池的电化学性能,提出水基锂离子电池目前的发展方向是提高比容量和循环稳定性.

  17. Hydrogenation of the rare earth alloys for production negative electrodes of nickel-metal hydride batteries; Hidrogenacao de ligas a base de terras raras para fabricacao de eletrodos negativos de baterias de niquel-hidreto metalico

    Energy Technology Data Exchange (ETDEWEB)

    Casini, Julio Cesar Serafim

    2011-07-01

    In this work were studied of La{sub 0.7-x}Mg{sub x} Pr{sub 0.3}Al{sub 0.3}Mn{sub 0.4}Co{sub 0.5}Ni{sub 3.8} (X = 0 and 0.7) alloys for negative electrodes of the nickel-metal hydride batteries. The hydrogenation of the alloys was performed varying pressing of H{sub 2} (2 and 10 bar) and temperature (room and 500 Degree-Celsius ). The discharge capacity of the nic kel-metal hydride batteries were analyzed in ARBIN BT- 4 electrical test equipment. The as-cast alloys were analyzed by scanning electron microscopy (SEM), energy disperse spectroscopy (EDX) and X-Ray diffraction. The increasing Mg addition in the alloy increases maximum discharge capacity but decrease cycle life of the batteries. The maximum discharge capacity was obtained with the Mg{sub 0.7}Pr{sub 0.3}Al{sub 0.3}Mn{sub 0.4}Co{sub 0.5}Ni{sub 3.8} alloy (60 mAh) and the battery which presented the best performance was La{sub 0.4}Mg{sub 0.3}Pr{sub 0.3}Al{sub 0.3}Mn{sub 0.4}Co{sub 0.5}Ni{sub 3.8} alloy (53 mAh and 150 cycles). The H{sub 2} capability of absorption was diminished for increased Mg addition and no such effect occurs for Mg{sub 0.7}Pr{sub 0.3}Al{sub 0.3}Mn{sub 0.4}Co{sub 0.5}Ni{sub 3.8} alloy. (author)

  18. 基于转化反应机制的锂离子电池电极材料研究进展%Progress of Electrode Materials Entailing Conversion Reaction for Li-ion Batteries

    Institute of Scientific and Technical Information of China (English)

    吴超; 崔永丽; 庄全超; 徐守冬; 沈明芳; 史月丽; 孙智

    2011-01-01

    基于转化反应机制实现储锂功能的电极材料的研究和开发是提高锂离子电池性能,尤其是其可逆循环容量的重要方法,对于锂离子电池未来的发展有着非常重要的意义。本文综述近年来基于转化反应机制实现储锂功能的锂离子电池电极材料的研究进展,介绍了转化反应机制等新概念,重点讨论了基于转化反应机制实现储锂功能的简单过渡金属化合物电极材料的电化学性能、电极界面特性及其电化学性能改进的方法,最后展望了基于转化反应机制实现储锂功能的锂离子电池电极材料的未来发展。%The development of electrode materials entailing conversion reactions were very important methods for improving the performance of Li-ion batteries,especially for improving its reversible capacity upon cycling.In this paper,the progresses of the use of transition metal compounds that react with Li through conversion reactions as both positive and negative electrode materials in Li-ion batteries were reviewed,the mechanisms of the conversion reactions were introduced,and several factors currently handicapping the applicability of electrode materials entailing conversion reactions were also discussed.Emphasis was put on the electrochemical behavior,the properties of electrode/electrolyte interfaces and the methods for improving the performance of these transition metal compounds entailing conversion reactions.At last,the directions of future research of electrode materials through conversion reactions were put forward.

  19. Spatial atomic layer deposition on flexible porous substrates: ZnO on anodic aluminum oxide films and Al{sub 2}O{sub 3} on Li ion battery electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Sharma, Kashish [Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309 (United States); Routkevitch, Dmitri; Varaksa, Natalia [InRedox, Longmont, Colorado 80544 (United States); George, Steven M., E-mail: Steven.George@Colorado.Edu [Department of Chemistry and Biochemistry, University of Colorado, Boulder, Colorado 80309 and Department of Mechanical Engineering, University of Colorado, Boulder, Colorado 80309 (United States)

    2016-01-15

    Spatial atomic layer deposition (S-ALD) was examined on flexible porous substrates utilizing a rotating cylinder reactor to perform the S-ALD. S-ALD was first explored on flexible polyethylene terephthalate polymer substrates to obtain S-ALD growth rates on flat surfaces. ZnO ALD with diethylzinc and ozone as the reactants at 50 °C was the model S-ALD system. ZnO S-ALD was then performed on nanoporous flexible anodic aluminum oxide (AAO) films. ZnO S-ALD in porous substrates depends on the pore diameter, pore aspect ratio, and reactant exposure time that define the gas transport. To evaluate these parameters, the Zn coverage profiles in the pores of the AAO films were measured using energy dispersive spectroscopy (EDS). EDS measurements were conducted for different reaction conditions and AAO pore geometries. Substrate speeds and reactant pulse durations were defined by rotating cylinder rates of 10, 100, and 200 revolutions per minute (RPM). AAO pore diameters of 10, 25, 50, and 100 nm were utilized with a pore length of 25 μm. Uniform Zn coverage profiles were obtained at 10 RPM and pore diameters of 100 nm. The Zn coverage was less uniform at higher RPM values and smaller pore diameters. These results indicate that S-ALD into porous substrates is feasible under certain reaction conditions. S-ALD was then performed on porous Li ion battery electrodes to test S-ALD on a technologically important porous substrate. Li{sub 0.20}Mn{sub 0.54}Ni{sub 0.13}Co{sub 0.13}O{sub 2} electrodes on flexible metal foil were coated with Al{sub 2}O{sub 3} using 2–5 Al{sub 2}O{sub 3} ALD cycles. The Al{sub 2}O{sub 3} ALD was performed in the S-ALD reactor at a rotating cylinder rate of 10 RPM using trimethylaluminum and ozone as the reactants at 50 °C. The capacity of the electrodes was then tested versus number of charge–discharge cycles. These measurements revealed that the Al{sub 2}O{sub 3} S-ALD coating on the electrodes enhanced the capacity stability. This S

  20. First-cycle defect evolution of Li1-xNi1/3Mn1/3Co1/3O2 lithium ion battery electrodes investigated by positron annihilation spectroscopy

    Science.gov (United States)

    Seidlmayer, Stefan; Buchberger, Irmgard; Reiner, Markus; Gigl, Thomas; Gilles, Ralph; Gasteiger, Hubert A.; Hugenschmidt, Christoph

    2016-12-01

    In this study the structure and evolution of vacancy type defects in lithium ion batteries are investigated in respect of crystallographic properties. The relation between positron annihilation and electronic structure is discussed in terms of structural dynamics during the lithiation process. Samples of Li1-xNi1/3Mn1/3Co1/3O2 (NMC-111) electrodes with decreasing lithium content (x = 0-0.7) covering the whole range of state of charge were electrochemically prepared for the non-destructive analysis using positron coincidence Doppler broadening spectroscopy (CDBS). The positron measurements allowed us to observe the evolution of the defect structure caused by the delithiation process in the NMC-111 electrodes. The combination of CDBS with X-ray diffraction for the characterization of the lattice structures enabled the analysis of the well-known kinetic-hindrance-effect in the first charge-discharge cycle and possible implications of vacancy ordering. In particular, CDBS revealed the highest degree of relithiation after discharge to 3.0 V at 55 °C. For the first time, we report on the successful application of CDBS on NMC-111 electrodes yielding new insights in the important role of defects caused by the delithiation process and the kinetic hindrance effect.

  1. 钛基聚阴离子型离子电池电极材料的研究进展%Study Progress in Ti-based Polyanionic Compound as Electrode Material for Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    孙艳茹; 彭祥倩; 朱明英; 盖利刚

    2015-01-01

    As ion battery has received much attention, it becomes a hot research topic to find a suitable electrode material. Ti-based polyanionic ion electrode materials have attracted increasing interest due to their excellent thermal stability and stable three-dimensional framework. This paper reviews several types of Ti-base polyanionic electrode materials, especially titanium pyrophosphate and Nasicon-type phosphate,and presents some major issues in the following research.%随着离子电池受到越来越多的重视,寻找合适的电极材料成为研究的热点。钛基聚阴离子型电极材料由于其热稳定性好、三维框架稳定等优良特性引起人们的关注。本文介绍了几种钛基聚阴离子型离子电池电极材料的研究现状,重点分析了焦磷酸钛和Nasicon型磷酸盐这两类材料的结构及其作为电极材料的研究进展,并提出了今后需要研究的一些主要问题。

  2. Structure analyses using X-ray photoelectron spectroscopy and X-ray absorption near edge structure for amorphous MS3 (M: Ti, Mo) electrodes in all-solid-state lithium batteries

    Science.gov (United States)

    Matsuyama, Takuya; Deguchi, Minako; Mitsuhara, Kei; Ohta, Toshiaki; Mori, Takuya; Orikasa, Yuki; Uchimoto, Yoshiharu; Kowada, Yoshiyuki; Hayashi, Akitoshi; Tatsumisago, Masahiro

    2016-05-01

    Electronic structure changes of sulfurs in amorphous TiS3 and MoS3 for positive electrodes of all-solid-state lithium batteries are examined by X-ray photoelectron spectroscopy (XPS) and the X-ray absorption near edge structure (XANES). The all-solid-state cell with amorphous TiS3 electrode shows the reversible capacity of about 510 mAh g-1 for 10 cycles with sulfur-redox in amorphous TiS3 during charge-discharge process. On the other hand, the cell with amorphous MoS3 shows the 1st reversible capacity of about 720 mAh g-1. The obtained capacity is based on the redox of both sulfur and molybdenum in amorphous MoS3. The irreversible capacity of about 50 mAh g-1 is observed at the 1st cycle, which is attributed to the irreversible electronic structure change of sulfur during the 1st cycle. The electronic structure of sulfur in amorphous MoS3 after the 10th charge is similar to that after the 1st charge. Therefore, the all-solid-state cell with amorphous MoS3 electrode shows relatively good cyclability after the 1st cycle.

  3. A new NASICON-type polyanion, Li{sub x}Ni{sub 2}(MoO{sub 4}){sub 3} as 3-V class positive electrode material for rechargeable lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Begam, K.M.; Michael, M.S.; Prabaharan, S.R.S. [Advanced Power Sources Laboratory, Multimedia University, Faculty of Engineering, Center for Smart Systems and Innovation, Cyberjaya 63100 (Malaysia); Taufiq-Yap, Y.H. [Department of Chemistry, Universiti Putra Malaysia, 43400 Serdang, Selangor D.H. (Malaysia)

    2004-08-31

    This paper presents our success in synthesizing a new framework type Li{sub x}Ni{sub 2}(MoO{sub 4}){sub 3} (0=electrode material in rechargeable lithium-containing batteries. The morphology of the heated product was found to be composed of soft agglomerates embedded by submicrometre spherical grains. The electrode-active character of the new material was examined in a two-electrode configuration employing a Li{sup +} non-aqueous electrolyte environment. Slow scan cyclic voltammetry (SSCV) revealed the redox property of the material between the voltage window 3.5 and 1.5 V. Galvanostatic tests exhibited a well discernible discharge-charge profile with a reversible capacity of 170 mA h/g over the potential window of 3.5-1.5 V.

  4. Studies on the electrode material for the all vanadium redox flow battery%全钒氧化还原流体电池电极材料的研究

    Institute of Scientific and Technical Information of China (English)

    李俊杰; 朱扬清; 杨华铨

    2001-01-01

    Various electrode material has been studied at 1.1 mol/L VOSO4 solution in 2 mol/L H2SO4 as electrolyte,using both cycilic voltammetry and A.C.impedance.The research result:the property of carbon electrodes is better then metals.Carbon electrodes may be used in vanadium battery.%选用不同类型的电极材料在1.1 mol/L VOSO4和2 mol/L H2SO4组成的电解液中进行循环伏安、交流阻抗研究,观察电极材料氧化还原的可逆性,研究结果表明:碳材料的电极比金属电极的性能好,可望用碳类材料作钒电池的电极材料.

  5. Button batteries

    Science.gov (United States)

    Swallowing batteries ... These devices use button batteries: Calculators Cameras Hearing aids Penlights Watches ... If a person puts the battery up their nose and breathes it further in, ... problems Cough Pneumonia (if the battery goes unnoticed) ...

  6. Understanding Structure-Function Relationship in Hybrid Co3O4-Fe2O3/C Lithium-Ion Battery Electrodes.

    Science.gov (United States)

    Sultana, Irin; Rahman, Md Mokhlesur; Ramireddy, Thrinathreddy; Sharma, Neeraj; Poddar, Debasis; Khalid, Abbas; Zhang, Hongzhou; Chen, Ying; Glushenkov, Alexey M

    2015-09-23

    A range of high-capacity Li-ion anode materials (conversion reactions with lithium) suffer from poor cycling stability and limited high-rate performance. These issues can be addressed through hybridization of multiple nanostructured components in an electrode. Using a Co3O4-Fe2O3/C system as an example, we demonstrate that the cycling stability and rate performance are improved in a hybrid electrode. The hybrid Co3O4-Fe2O3/C electrode exhibits long-term cycling stability (300 cycles) at a moderate current rate with a retained capacity of approximately 700 mAh g(-1). The reversible capacity of the Co3O4-Fe2O3/C electrode is still about 400 mAh g(-1) (above the theoretical capacity of graphite) at a high current rate of ca. 3 A g(-1), whereas Co3O4-Fe2O3, Fe2O3/C, and Co3O4/C electrodes (used as controls) are unable to operate as effectively under identical testing conditions. To understand the structure-function relationship in the hybrid electrode and the reasons for the enhanced cycling stability, we employed a combination of ex situ and in situ techniques. Our results indicate that the improvements in the hybrid electrode originate from the combination of sequential electrochemical activity of the transition metal oxides with an enhanced electronic conductivity provided by percolating carbon chains.

  7. Direct Observation of Active Material Concentration Gradients and Crystallinity Breakdown in LiFePO4 Electrodes During Charge/Discharge Cycling of Lithium Batteries.

    Science.gov (United States)

    Roberts, Matthew R; Madsen, Alex; Nicklin, Chris; Rawle, Jonathan; Palmer, Michael G; Owen, John R; Hector, Andrew L

    2014-04-03

    The phase changes that occur during discharge of an electrode comprised of LiFePO4, carbon, and PTFE binder have been studied in lithium half cells by using X-ray diffraction measurements in reflection geometry. Differences in the state of charge between the front and the back of LiFePO4 electrodes have been visualized. By modifying the X-ray incident angle the depth of penetration of the X-ray beam into the electrode was altered, allowing for the examination of any concentration gradients that were present within the electrode. At high rates of discharge the electrode side facing the current collector underwent limited lithium insertion while the electrode as a whole underwent greater than 50% of discharge. This behavior is consistent with depletion at high rate of the lithium content of the electrolyte contained in the electrode pores. Increases in the diffraction peak widths indicated a breakdown of crystallinity within the active material during cycling even during the relatively short duration of these experiments, which can also be linked to cycling at high rate.

  8. 全钒液流电池用PTFE-碳纳米管电极的性能%Characteristics of graphite based composite electrodes containing carbon nanotubes for vanadium redox flow batteries

    Institute of Scientific and Technical Information of China (English)

    李丹丹; 褚有群; 李雯雯; 马淳安

    2013-01-01

      以聚四氟乙烯(PTFE)为黏结剂制备了不同组分的石墨粉(GP)和多壁碳纳米管(MWCNT)复合电极,采用恒电位阶跃、循环伏安、电化学阻抗谱及恒电流充放电等方法系统考察了 GP-MWCNT 复合电极在全钒液流电池(VRFB)体系中的电化学性能。实验结果表明:复合电极中MWCNT含量的增加有利于VRFB正、负极反应的进行,纯MWCNT电极表现出最优的电化学性能;以纯MWCNT电极为正、负极构建的VRFB电池在30 mA/cm2的恒电流充放电条件下表现出了良好的稳定性和电化学性能,电流效率、电压效率和能量效率分别为96%、87%和84%。%Graphite (GP) based composite electrodes containing multi-walled carbon nanotube (MWCNT) were prepared for vanadium redox flow batteries (VRFB) using polytetrafluoroethylene (PTFE) as binding agent. Electrochemical performance of the GP-MWCNT composite electrodes was characterized by chronoamperometry, cyclic voltammetry and electrochemical impedance spectroscopy. The results showed that both positive and negative electrode reactions of VRFB benefited from the use of more MWCNT in the composite electrode, and the best electrochemical performance was obtained with pure MWCNT electrode. A VRFB was therefore constructed using pure MWCNT electrodes as both the positive and negative electrodes. Preliminary charge/discharge tests at a current density of 30 mA/cm2 demonstrated that the VRFB had a good stability and electrochemical performance. The current efficiency, voltage efficiency and energy efficiency were 96%, 87%and 84%, respectively.

  9. Lithium Ion Battery Anode Aging Mechanisms

    Directory of Open Access Journals (Sweden)

    Victor Agubra

    2013-03-01

    Full Text Available Degradation mechanisms such as lithium plating, growth of the passivated surface film layer on the electrodes and loss of both recyclable lithium ions and electrode material adversely affect the longevity of the lithium ion battery. The anode electrode is very vulnerable to these degradation mechanisms. In this paper, the most common aging mechanisms occurring at the anode during the operation of the lithium battery, as well as some approaches for minimizing the degradation are reviewed.

  10. Lithium Ion Battery Anode Aging Mechanisms

    OpenAIRE

    Victor Agubra; Jeffrey Fergus

    2013-01-01

    Degradation mechanisms such as lithium plating, growth of the passivated surface film layer on the electrodes and loss of both recyclable lithium ions and electrode material adversely affect the longevity of the lithium ion battery. The anode electrode is very vulnerable to these degradation mechanisms. In this paper, the most common aging mechanisms occurring at the anode during the operation of the lithium battery, as well as some approaches for minimizing the degradation are reviewed.

  11. Electrochemical and impedance investigation of the effect of lithium malonate on the performance of natural graphite electrodes in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Xiao-Guang; Dai, Sheng [Chemical Sciences Division, Oak Ridge National Laboratory, One Bethel Valley Road, Oak Ridge, TN 37831 (United States)

    2010-07-01

    Lithium malonate (LM) was coated on the surface of a natural graphite (NG) electrode, which was then tested as the negative electrode in the electrolytes of 0.9 M LiPF{sub 6}/EC-PC-DMC (1/1/3, w/w/w) and 1.0 M LiBF{sub 4}/EC-PC-DMC (1/1/3, w/w/w) under a current density of 0.075 mA cm{sup -2}. LM was also used as an additive to the electrolyte of 1.0 M LiPF{sub 6}/EC-DMC-DEC (1/1/1, v/v/v) and tested on a bare graphite electrode. It was found that both the surface coating and the additive approach were effective in improving first charge-discharge capacity and coulomb efficiency. Electrochemical impedance spectra showed that the decreased interfacial impedance was coupled with improved coulomb efficiency of the cells using coated graphite electrodes. Cyclic voltammograms (CVs) on fresh bare and coated natural graphite electrodes confirmed that all the improvement in the half-cell performance was due to the suppression of the solvent decomposition through the surface modification with LM. The CV data also showed that the carbonate electrolyte with LM as the additive was not stable against oxidation, which resulted in lower capacity of the full cell with commercial graphite and LiCoO{sub 2} electrodes. (author)

  12. Electrochemical and impedance investigation of the effect of lithium malonate on the performance of natural graphite electrodes in lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Sun, Xiao-Guang [ORNL; Dai, Sheng [ORNL

    2010-01-01

    Lithium malonate (LM) was coated on the surface of a natural graphite (NG) electrode, which was then tested as the negative electrode in the electrolytes of 0.9 M LiPF6/EC-PC-DMC (1/1/3, by weight) and 1.0 M LiBF4/EC-PC-DMC (1/1/3, by weight) under a current density of 0.075 mA cm-2. LM was also used as an additive to the electrolyte of 1.0 M LiPF6/EC-DMC-DEC (1/1/1, by volume) and tested on a bare graphite electrode. It was found that both the surface coating and the additive approach were effective in improving first charge discharge capacity and coulomb efficiency. Electrochemical impedance spectra showed that the decreased interfacial impedance was coupled with improved coulomb efficiency of the cells using coated graphite electrodes. Cyclic voltammograms (CVs) on fresh bare and coated natural graphite electrodes confirmed that all the improvement in the half-cell performance was due to the suppression of the solvent decomposition through the surface modification with LM. The CV data also showed that the carbonate electrolyte with LM as the additive was not stable against oxidation, which resulted in lower capacity of the full cell with commercial graphite and LiCoO2 electrodes.

  13. Secondary alkaline batteries

    Science.gov (United States)

    McBreen, J.

    1984-03-01

    The overall reactions (charge/discharge characteristics); electrode structures and materials; and cell construction are studied for nickel oxide-cadmium, nickel oxide-iron, nickel oxide-hydrogen, nickel oxide-zinc, silver oxide-zinc, and silver oxide-cadmium, silver oxide-iron, and manganese dioxide-zinc batteries.

  14. Sealed nickel-cadmium battery

    Energy Technology Data Exchange (ETDEWEB)

    1989-08-15

    Overcharge protection, and especially the chargeability of a sealed Ni/Cd battery with high currents is improved by rolling a carbon-containing powdered material into the surface of the negative electrode, which material catalyzes the reduction of oxygen. Wetting of the electrode with a Tylose dispersion prior to application of the powder (by powdering, vibration or in an agitator) improves the adhesion of the powder. The cadmium electrode thus prepared combines in itself the functions of a negative principal electrode and of an auxiliary oxygen electrode.

  15. Self-assembled sulfur/reduced graphene oxide nanoribbon paper as a free-standing electrode for high performance lithium-sulfur batteries.

    Science.gov (United States)

    Liu, Yang; Wang, Xuzhen; Dong, Yanfeng; Tang, Yongchao; Wang, Luxiang; Jia, Dianzeng; Zhao, Zongbin; Qiu, Jieshan

    2016-10-25

    Flexible, interconnected sulfur/reduced graphene oxide nanoribbon paper (S/RGONRP) is synthesized through S(2-) reduction and evaporation induced self-assembly processes. The in situ formed sulfur atoms chemically bonded with the surface of reduced graphene oxide nanoribbons and were physically trapped by the compact assembly, which make the hybrid a suitable cathode material for lithium-sulfur batteries.

  16. An ionization chamber with magnetic levitated electrodes

    CERN Document Server

    Kawaguchi, T

    1999-01-01

    A new type of ionization chamber which has magnetically levitated electrodes has been developed. The electrodes are supplied voltages for the repelling of ions by a battery which is also levitated with the electrodes. The characteristics of this ionization chamber are investigated in this paper.

  17. Recovery of Cobalt from Spent Forth Nickel Electrode Plates of Secondary Batteries%从二次电池废泡沫式镍极板中回收钴

    Institute of Scientific and Technical Information of China (English)

    江丽; 张志清; 陈刚; 周晓明; 盘晓然

    2001-01-01

    A hydrometallurgical process for recovery of Co2+ from P507 loading Co2+and Cd2+ has been investigated.The P507 is intermediate product in the course of separating nickel from spent forth nickel electrode plate yielded in producing secondary batteries.Optimium conditions for extraction Co2+ and Cd2+ with P204 are given.%研究了用P204从负载Co2+和Cd2+的P507有机溶液中回收Co2+的工艺。此P507有机溶液是用P507从二次电池废泡沫式镍极板中回收镍流程中的中间产物。给出了P204萃取分离钴、隔的最佳工艺条件。

  18. Bastões de grafite reciclados de baterias comuns e seu uso como eletrodo modificado em hidrogenação eletrocatalítica de alguns substratos orgânicos Graphite sticks recycled from common batteries and their use as a modified electrode in electrocatalytic hydrogenation of some organic substrates

    Directory of Open Access Journals (Sweden)

    Renata C. Z. Lofrano

    2002-12-01

    Full Text Available This paper presents some results on the employ of recycled graphite electrode obtained from used common 1.5 V batteries in the preparation of modified electrode and the electrocatalytical hydrogenation of benzaldehyde and of n-valeraldehyde. This inexpensive and easy to obtain electrode was prepared by coating it with a 1:1 mixed film of poly-(allylfenil ether: poly-[allyl p-(2-ethylammonium benzene ether] and introduction of dispersed platinum particles by ion exchange and reduction of PtCl4-2. Electroreduction of H+ from aqueous H2SO4 using the proposed electrode hydrogenated the substrates in a way comparable with that of vitreous carbon electrode.

  19. 自由基聚合物——一类新颖的高性能二次电池材料%Radical Polymer —A New Class of High Performance Electrode Materials for Rechargeable Batteries

    Institute of Scientific and Technical Information of China (English)

    赵瑞瑞; 朱利敏; 杨汉西

    2011-01-01

    Radical polymers are aliphatic or nonconjugated polymers bearing organic redox radicals as pendant groups on their structural unit. These radical sites populated in large densities allow the electrochemical redox reaction taking place through the polymer layer by redox gradient-driven electron transport and behave as electroactive centers. Since radical polymer can be designed with a large population of redox radicals and electron exchange between the radical sites are usually very fast, they are considered as a new class of charge storage and transport materials with the possibility to provide high electrical storage capacity and high charge-discharge rate capability. Particularly, these polymers are completely organic with the advantage of being fully substainable, they are ideal for the displacement of inorganic materials in diverse applications such as electrochemical supercapacitors,photovoltaic cells and rechargeable batteries. This paper is intended to review the structural characteristics,electrochemical reaction mechanisms and current development status of the radical polymers as electode-active materials, with focus on the technological challenges and ongoing research strategies of these novel electrode materials as used for construction of high capacity and high rate rechargeable batteries. Also, the problems in the development of radical polymer electrodes are discussed.%自由基聚合物是一种新近发展迅速的电荷储存与传输材料,在电化学超级电容器、光电转换器件、二次电池等方面具有诱人的应用前景.本文着重介绍这类新颖电极材料的结构特征、电化学反应机制,以及国内外的研究发展现状;分析了采用自由基聚合物构建新型二次电池的技术途径和发展趋势.

  20. 全钒离子氧化还原液流电池电极活性物质的研究%Study on Electrode Active Materials for all Vanadium Redox Flow Battery

    Institute of Scientific and Technical Information of China (English)

    张环华; 肖楚民; 张平民

    2000-01-01

    介绍了以VOSO4为原料,电解制备全钒离子氧化还原液流电池的正极活性物质V(Ⅴ)盐和负极活性物V(Ⅱ)盐,并用循环伏安法研究了它们在石墨电极上的电化学性质。结果表明,在硫酸溶液中,作为全钒电池的正极和负极V(Ⅴ)/V(Ⅳ)和V(Ⅲ)/V(Ⅱ)电对在石墨电极上的氧化还原反应均为单电子准可逆过程.%Electrolytic method to prepare positive and negative active materials from VOSO4 sulphuric acid solution for all vanadium redox flow battery is described. V(Ⅴ)salt is obtained in anode area and V(Ⅱ) salt is in cathode area. The electrochemical behaviour of the two series salt on graphite electrode have also been studied by cyclic voltammetry. The results showed that the redox reactions of V(Ⅴ)/V(Ⅳ) and V(Ⅲ)/V(Ⅱ) couples in sulfuric adid,which are used for anolyte and catholyte in a redox flow battery,is qusi-reversible.

  1. Effects of Propylene Carbonate Content in CsPF6-Containing Electrolytes on the Enhanced Performances of Graphite Electrode for Lithium-Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zheng, Jianming; Yan, Pengfei; Cao, Ruiguo; Xiang, Hongfa; Engelhard, Mark H.; Polzin, Bryant; Wang, Chong M.; Zhang, Jiguang; Xu, Wu

    2016-02-10

    Cesium salt has been demonstrated as an efficient electrolyte additive in suppressing the lithium (Li) dendrite formation and directing the formation of an ultrathin and stable solid electrolyte interphase (SEI) even in propylene carbonate (PC)-ethylene carbonate (EC)-based electrolytes. Here, we further investigate the effect of PC content in the presence of CsPF6 additive (0.05 M) on the performances of graphite electrode in Li||graphite half cells and in graphite||LiNi0.80Co0.15Al0.05O2 (NCA) full cells. It is found that the performance of graphite electrode is also affected by PC content even though CsPF6 additive is present in the electrolytes. An optimal PC content of 20% by weight in the solvent mixtures is identified. The enhanced electrochemical performance of graphite electrode is attributed to the synergistic effects of the Cs+ additive and the PC solvent. The formation of a robust, ultrathin and compact SEI layer containing lithium-enriched species on the graphite electrode, directed by Cs+, effectively suppresses the PC co-intercalation and thus prevents the graphite exfoliation. This SEI layer is only permeable for de-solvated Li+ ions and allows fast Li+ ion transport through it, which therefore largely alleviates the Li dendrite formation on graphite electrode during lithiation even at high current densities. The presence of low-melting-point PC solvent also enables the sustainable operation of the graphite||NCA full cells under a wide spectrum of temperatures. The fundamental findings of this work shed light on the importance of manipulating/maintaining the electrode/electrolyte interphasial stability in a variety of energy storage devices.

  2. Design and Evaluation of a Three Dimensionally Ordered Macroporous Structure within a Highly Patterned Cylindrical Sn-Ni Electrode for Advanced Lithium Ion Batteries

    Directory of Open Access Journals (Sweden)

    Yongcheng Jin

    2013-01-01

    Full Text Available A 3-dimensionally ordered macroporous (3DOM structure within a highly patterned cylindrical Sn-Ni alloy electrode was tailored by using various monodispersed polystyrene (PS templates via a colloidal crystal templating process coupled with an electroplating process. The pore size and the wall thickness in the “inverse opal” 3DOM structure were increased with increasing the size of the PS template beads used in this study. The electrochemical performance of prepared electrodes was examined in order to reveal the correlation between the rate capability and the 3DOM structure. Except the electrode with 1.2 μm pores, the discharge capacities gradually decreased with increasing the current density, showing a capacity conservation ratio of 87% for the electrode with 0.5 μm pores and that of 84% for the electrode with 3.0 μm pores when the current density increased from 0.05 mA cm−2 to 2.0 mA cm−2. The reason for this difference is attributed to the fact that the wall thickness of less than 0.5 μm in the electrode with 1.2 μm pores has a short Li+ diffusion distance in solid-state walls. In addition, it is expected that high regularity of 3DOM structure plays a great role on rate capability. Consequently, the 3DOM structure prepared from 1.2 μm PS template beads was favorable for improving the rate capability.

  3. In-situ, Real-Time Monitoring of Mechanical and Chemical Structure Changes in a V2O5 Battery Electrode Using a MEMS Optical Sensor

    Energy Technology Data Exchange (ETDEWEB)

    Jung, H. [University of Maryland; Gerasopoulos, K. [University of Maryland; Gnerlich, Markus [University of Maryland; Talin, A. Alec [Sandia National Laboratories; Ghodssi, Reza [University of Maryland

    2014-06-01

    This work presents the first demonstration of a MEMS optical sensor for in-situ, real-time monitoring of both mechanical and chemical structure evolutions in a V2O5 lithium-ion battery (LIB) cathode during battery operation. A reflective membrane forms one side of a Fabry-Perot (FP) interferometer, while the other side is coated with V2O5 and exposed to electrolyte in a half-cell LIB. Using one microscope and two laser sources, both the induced membrane deflection and the corresponding Raman intensity changes are observed during lithium cycling. Results are in good agreement with the expected mechanical behavior and disorder change of the V2O5 layers, highlighting the significant potential of MEMS as enabling tools for advanced scientific investigations.

  4. A hierarchical three-dimensional NiCo2O4 nanowire array/carbon cloth as an air electrode for nonaqueous Li-air batteries.

    Science.gov (United States)

    Liu, Wei-Ming; Gao, Ting-Ting; Yang, Yin; Sun, Qian; Fu, Zheng-Wen

    2013-10-14

    A 3D NiCo2O4 nanowire array/carbon cloth (NCONW/CC) was employed as the cathode for Li-air batteries with a non-aqueous electrolyte. After its discharge, novel porous ball-like Li2O2 was found to be deposited on the tip of NiCo2O4 nanowires. The special structure of Li2O2 and active sites of catalysts are also discussed.

  5. 新型光辅助充电锂离子电池用电极材料%New kind of electrode materials used for photo-rechargeable lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    谢潇怡; 吴锋; 吴伯荣

    2011-01-01

    The solar cells and lithium-ion secondary battery has been commercialized today, but both of them have their own development space. Because there are respective irreplaceable advantages and unsolvable weaknesses in the two battery systems, the photo-rechargeable lithium-ion battery is emerging. The relative literatures were reviewed, but up till now, there was no significant progress in this field of electrode materials. A lot of materials have been investigated, and the results show that there are momentous factors to take into account, such as matching of the energy levels, high redox potentials of the photo-convert carriers, surface roughness of the materials and the particle size. To sum it up, there is a long and formidable way to find high performance material for the photo-rechargeable lithium-ion batteries.%在太阳电池和锂离子电池已经商业化的今天,各自都还有发展空间.鉴于两大电池体系有各自不可替代的优势及无法解决的弱点,可光辅助充电的锂离子电池将它们有机结合起来形成了新型电池.纵观各项相关文献,目前为止,相关电极材料鲜有显著的研究进展.科学家们使用了很多材料进行探索,但是实验结果表明,材料间的能级匹配、光生载流子的高氧化还原电位、材料的表面粗糙度和粒子的粒径大小等等都是需要考虑的重要因素.最终要找到一个既具有高光电转换效率又具有高储存容量的材料还有艰难而漫长的道路.

  6. Computer Aided Battery Engineering Consortium

    Energy Technology Data Exchange (ETDEWEB)

    Pesaran, Ahmad

    2016-06-07

    A multi-national lab collaborative team was assembled that includes experts from academia and industry to enhance recently developed Computer-Aided Battery Engineering for Electric Drive Vehicles (CAEBAT)-II battery crush modeling tools and to develop microstructure models for electrode design - both computationally efficient. Task 1. The new Multi-Scale Multi-Domain model framework (GH-MSMD) provides 100x to 1,000x computation speed-up in battery electrochemical/thermal simulation while retaining modularity of particles and electrode-, cell-, and pack-level domains. The increased speed enables direct use of the full model in parameter identification. Task 2. Mechanical-electrochemical-thermal (MECT) models for mechanical abuse simulation were simultaneously coupled, enabling simultaneous modeling of electrochemical reactions during the short circuit, when necessary. The interactions between mechanical failure and battery cell performance were studied, and the flexibility of the model for various batteries structures and loading conditions was improved. Model validation is ongoing to compare with test data from Sandia National Laboratories. The ABDT tool was established in ANSYS. Task 3. Microstructural modeling was conducted to enhance next-generation electrode designs. This 3- year project will validate models for a variety of electrodes, complementing Advanced Battery Research programs. Prototype tools have been developed for electrochemical simulation and geometric reconstruction.

  7. Anodes - Materials for negative electrodes in electrochemical energy technology

    Science.gov (United States)

    Holze, Rudolf

    2014-06-01

    The basic concepts of electrodes and electrochemical cells (including both galvanic and electrolytic ones) are introduced and illustrated with practical examples. Particular attention is paid to negative electrodes in primary and secondary cells, fuel cell electrodes and electrodes in redox flow batteries. General features and arguments pertaining to selection, optimization and further development are highlighted.

  8. Coated carbon nanotube array electrodes

    Science.gov (United States)

    Ren, Zhifeng; Wen, Jian; Chen, Jinghua; Huang, Zhongping; Wang, Dezhi

    2008-10-28

    The present invention provides conductive carbon nanotube (CNT) electrode materials comprising aligned CNT substrates coated with an electrically conducting polymer, and the fabrication of electrodes for use in high performance electrical energy storage devices. In particular, the present invention provides conductive CNTs electrode material whose electrical properties render them especially suitable for use in high efficiency rechargeable batteries. The present invention also provides methods for obtaining surface modified conductive CNT electrode materials comprising an array of individual linear, aligned CNTs having a uniform surface coating of an electrically conductive polymer such as polypyrrole, and their use in electrical energy storage devices.

  9. Electrochemical Activity of a La0.9Ca0.1Co1−xFexO3 Catalyst for a Zinc Air Battery Electrode

    OpenAIRE

    Seungwook Eom; Seyoung Ahn; Sanghwan Jeong

    2015-01-01

    The optimum composition of cathode catalyst has been studied for rechargeable zinc air battery application. La0.9Ca0.1Co1−xFexO3  (x=0–0.4) perovskite powders were prepared using the citrate method. The substitution ratio of Co2+ with Fe3+ cations was controlled in the range of 0–0.4. The optimum substitution ratio of Fe3+ cations was determined by electrochemical measurement of the air cathode composed of the catalyst, polytetrafluoroethylene (PTFE) binder, and Vulcan XC-72 carbon. The subst...

  10. Flexible lithium-ion planer thin-film battery

    KAUST Repository

    Kutbee, Arwa T.

    2016-02-03

    Commercialization of wearable electronics requires miniaturized, flexible power sources. Lithium ion battery is a strong candidate as the next generation high performance flexible battery. The development of flexible materials for battery electrodes suffers from the limited material choices. In this work, we present a flexible inorganic lithium-ion battery with no restrictions on the materials used. The battery showed an enhanced normalized capacity of 146 ??Ah/cm2.

  11. Anode properties and morphology evolution of three-dimensional lithium-ion battery electrodes comprising Ni-coated Si microchannel plates

    Energy Technology Data Exchange (ETDEWEB)

    Wang, Fei; Zhu, Shanshan; Li, Mai; Lou, Xuefeng; Hui, Keshuang; Xu, Shaohui; Yang, Pingxiong [Laboratory of Polar Materials and Devices, Ministry of Education, Department of Electronic Engineering, East China Normal University, Shanghai 200241 (China); Wang, Lianwei, E-mail: lwwang@ee.ecnu.edu.cn [Laboratory of Polar Materials and Devices, Ministry of Education, Department of Electronic Engineering, East China Normal University, Shanghai 200241 (China); Chen, Yiwei [Department of Physics, East China Normal University, Shanghai 200241 (China); Chu, Paul K. [Department of Physics and Material Sciences, City University of Hong Kong, Tat Chee Avenue, Kowloon, Hong Kong (China)

    2013-06-25

    Highlights: ► Decreasing the Li insertion/extraction level will improve the cyclic performances. ► The morphology of the Ni/Si-MCP after the galvanostatic cycles was examined. ► The mechanism of electrode fading was investigated and described. -- Abstract: Using lithium foils as the counter electrodes and Ni-coated Si microchannel plates (Si-MCPs) as the matrix and active materials, half-cells were fabricated and tested. Galvanostatic charge–discharge (C–D) measurements were conducted at 100 mA g{sup −1} between 0.05 and 1.5 V. By decreasing the Li insertion/extraction level, the Ni/Si-MCP anode retained the reversible discharge capacity of 1000 mA h g{sup −1} for 80 cycles and 500 mA h g{sup −1} for 104 cycles, respectively. The morphology of the Ni/Si-MCP after the galvanostatic cycles was examined by scanning electron microscope (SEM). Based on the results of electrochemical impedance spectroscopy (EIS) and energy-dispersive X-ray spectroscopy (EDS), the mechanism of electrode fading was investigated and described.

  12. Microstructural analysis of the ageing of pseudo-binary (Ti,Zr)Ni intermetallic compounds as negative electrodes of Ni-MH batteries

    Energy Technology Data Exchange (ETDEWEB)

    Guiose, B. [Equipe de Chimie Metallurgique des Terres Rares, ICMPE, UMR7182, CNRS, 2-8 rue Henri Dunant, 94320 Thiais Cedex (France); Cuevas, F. [Equipe de Chimie Metallurgique des Terres Rares, ICMPE, UMR7182, CNRS, 2-8 rue Henri Dunant, 94320 Thiais Cedex (France)], E-mail: cuevas@icmpe.cnrs.fr; Decamps, B.; Leroy, E.; Percheron-Guegan, A. [Equipe de Chimie Metallurgique des Terres Rares, ICMPE, UMR7182, CNRS, 2-8 rue Henri Dunant, 94320 Thiais Cedex (France)

    2009-04-01

    Ageing of Ti{sub 1.02-x}Zr{sub x}Ni{sub 0.98} (0 {<=} x {<=} 0.48) compounds during the electrochemical cycling in aqueous KOH electrolyte has been investigated. Microstructural and chemical characterisation, mostly conducted by transmission electron microscopy, show that for all electrodes their activation results from calendar KOH corrosion. After activation, Zr substituted compounds attain much higher capacity ({approx}350 mAh g{sup -1}) than the binary TiNi compound ({approx}150 mAh g{sup -1}) but their cycle-life is poor. The mechanism of electrode degradation differs for the binary and the substituted compounds. For TiNi, degradation is due to KOH corrosion whereas, for substituted compounds, it mainly results from the loss of electrical contact due to particle pulverisation. For all electrodes, KOH corrosion produces a double surface layer formed by an inner two-phase (Ni-NiO) nanocrystalline layer and an outer (Ti,Zr)O{sub 2} amorphous layer.

  13. Fully Coupled Simulation of Lithium Ion Battery Cell Performance

    Energy Technology Data Exchange (ETDEWEB)

    Trembacki, Bradley L. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Murthy, Jayathi Y. [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States); Roberts, Scott Alan [Sandia National Lab. (SNL-NM), Albuquerque, NM (United States)

    2015-09-01

    Lithium-ion battery particle-scale (non-porous electrode) simulations applied to resolved electrode geometries predict localized phenomena and can lead to better informed decisions on electrode design and manufacturing. This work develops and implements a fully-coupled finite volume methodology for the simulation of the electrochemical equations in a lithium-ion battery cell. The model implementation is used to investigate 3D battery electrode architectures that offer potential energy density and power density improvements over traditional layer-by-layer particle bed battery geometries. Advancement of micro-scale additive manufacturing techniques has made it possible to fabricate these 3D electrode microarchitectures. A variety of 3D battery electrode geometries are simulated and compared across various battery discharge rates and length scales in order to quantify performance trends and investigate geometrical factors that improve battery performance. The energy density and power density of the 3D battery microstructures are compared in several ways, including a uniform surface area to volume ratio comparison as well as a comparison requiring a minimum manufacturable feature size. Significant performance improvements over traditional particle bed electrode designs are observed, and electrode microarchitectures derived from minimal surfaces are shown to be superior. A reduced-order volume-averaged porous electrode theory formulation for these unique 3D batteries is also developed, allowing simulations on the full-battery scale. Electrode concentration gradients are modeled using the diffusion length method, and results for plate and cylinder electrode geometries are compared to particle-scale simulation results. Additionally, effective diffusion lengths that minimize error with respect to particle-scale results for gyroid and Schwarz P electrode microstructures are determined.

  14. A comparative study on the impact of different glymes and their derivatives as electrolyte solvents for graphite co-intercalation electrodes in lithium-ion and sodium-ion batteries.

    Science.gov (United States)

    Jache, Birte; Binder, Jan Oliver; Abe, Takeshi; Adelhelm, Philipp

    2016-06-07

    The abundance of sodium has recently sparked considerable interest in sodium-ion batteries (NIBs). Their similarity to conventional lithium-ion technology is obvious; however, the cell chemistry often significantly deviates. Graphite, although being the standard negative electrode in Li-ion batteries, is largely inactive for Na-ion storage in conventional non-aqueous carbonate-based electrolytes, for example. Very recently, it has been demonstrated that graphite can be activated for Na-ion storage in cells with ether-based electrolytes. The storage mechanism is based on co-intercalation of solvent molecules along with the Na-ions, forming ternary graphite intercalation compounds (t-GICs). This process is highly reversible but yet poorly understood. Here, we provide a comprehensive study on the formation and the stability of t-GICs. A series of ether solvents are being discussed: linear glymes with different chain lengths (mono-, di-, tri-, and tetraglyme), several derivatives with side groups as well as tetrahydrofuran (THF) as a cyclic ether and one crown ether. We show that the redox potentials shift depending on the ether chain length and mixing of ethers might enable tailoring of the redox behaviour. The inferior behaviour of triglyme is likely due to the less ideal ion coordination. Complementary experiments with lithium are made and demonstrate the superior behaviour of sodium. We find that the increase in graphene layer spacing during intercalation only slightly depends on the chain length and is in the range of 250%, and still mechanical stability is preserved. We further show the t-GICs possess chemical stability and demonstrate that the kinetically favoured charge transfer is probably due to the absence of a solid electrolyte interphase.

  15. Characterization and analysis of the negative electrode active materials in spent lithium-ion secondary batteries%废锂离子电池负极活性材料的分析测试

    Institute of Scientific and Technical Information of China (English)

    夏静; 张哲鸣; 贺文智; 李光明; 李心砚; 王琢璞; 李舒

    2013-01-01

    目前关于废锂离子电池资源化的研究主要集中在正极贵金属和负极铜材料的分离回收和精制方面,但对负极活性材料的资源化研究很少。本文采用XRD、SEM、GC-MS、ICP-AES等检测手段对废锂离子电池负极活性材料中石墨的结构、有机物的种类以及Li、Gu等金属的含量进行测试分析。结果显示,其主要组分石墨的本体结构基本无变化,仍保持完整的层状结构,但是其中含有一定量的有机物质,如有机电解质及增塑剂等。经过提纯,可以将其作为石墨原料进行资源化再利用;此外,稀有金属Li含量较高,为31.03 mg/g,分离回收的价值较高。%At present,the research on spent lithium-ion secondary batteries is mainly focused on the separation recovery and refinery of precious metals in positive materials and copper in negative materials. But the research on negative active materials is rare. In this paper,the negative electrode active materials in spent lithium-ion secondary batteries are tested by XRD、SEM、GC-MS、ICP-AES, including the structure of graphite,the kinds of organic matter,and metal contents. The results show that there is basically no change in the graphite material body structure,it still keeps the complete layer structure. However,it contains a certain amount of organic material,such as organic electrolyte and plasticizer,etc. It can be reused after purification. What is more,the concentration of Li is high,with the value of 31.03 mg/g. Regarding the recovery of negative electrode active materials,the separation recycling of Li also should be concerned.

  16. Electrochemical Activity of a La0.9Ca0.1Co1−xFexO3 Catalyst for a Zinc Air Battery Electrode

    Directory of Open Access Journals (Sweden)

    Seungwook Eom

    2015-01-01

    Full Text Available The optimum composition of cathode catalyst has been studied for rechargeable zinc air battery application. La0.9Ca0.1Co1−xFexO3  (x=0–0.4 perovskite powders were prepared using the citrate method. The substitution ratio of Co2+ with Fe3+ cations was controlled in the range of 0–0.4. The optimum substitution ratio of Fe3+ cations was determined by electrochemical measurement of the air cathode composed of the catalyst, polytetrafluoroethylene (PTFE binder, and Vulcan XC-72 carbon. The substitution by Fe enhanced the electrochemical performances of the catalysts. Considering oxygen reduction/evolution reactions and cyclability, we achieved optimum substitution level of x=0.1 in La0.9Ca0.1Co1−xFexO3.

  17. In situ La, Ce, and Nd L-edge X-ray absorption fine structure study of an intermetallic metal hydride electrode in an operating alkaline battery

    Energy Technology Data Exchange (ETDEWEB)

    Tryk, D.A.; Bae, I.T.; Scherson, D. [Case Western Reserve Univ., Cleveland, OH (United States). Dept. of Chemistry; Antonio, M.R. [Argonne National Lab., IL (United States). Chemistry Division; Jordan, G.W.; Huston, E.L. [Energizer Power Systems, Gainesville, FL (United States)

    1995-05-01

    The X-ray absorption fine structure of a technologically important MmL{sub 5} intermetallic compound (Mm = La{sub 0.52}Ce{sub 0.34}Nd{sub 0.10}Pr{sub 0.04}, L{sub 5} Ni{sub 3.5}Ca{sub 0.8}Mn{sub 0.3}Al{sub 0.4}) in the form of a hydrogen storage cathode was recorded in situ in the region 5440-6290 eV using an electrochemical cell which is essentially a fully functioning alkaline battery. Significant differences were observed in the X-ray absorption near edge structure (XANES) of all of the absorption edges (La, Ce, and Nd) between the uncharged and fully charged states. In particular, a clear increase in the intensity of the La and Nd L{sub III}-edge resonances (due to 2P{sub 3/2} {r_arrow} 5d electronic transitions) was found upon charging the cell. This phenomenon was attributed to an increase in the density of empty d-like states near the Fermi level following hydrogen injection into the lattice. Furthermore, the behavior of the Ca L{sub II,III}-edges of this battery material upon charging was nearly the same as that observed for the gas phase hydrogenation of the Ce{sub 2}Fe{sub 17} and Ce{sub 2}Fe{sub 14}B intermetallics reported in the literature.

  18. Separators for Lithium Ion Batteries

    Institute of Scientific and Technical Information of China (English)

    G.C.Li; H.P.Zhang; Y.P.Wu

    2007-01-01

    1 Results A separator for rechargeable batteries is a microporous membrane placed between electrodes of opposite polarity, keeping them apart to prevent electrical short circuits and at the same time allowing rapid transport of lithium ions that are needed to complete the circuit during the passage of current in an electrochemical cell, and thus plays a key role in determining the performance of the lithium ion battery. Here provides a comprehensive overview of various types of separators for lithium io...

  19. Tension Control System of Electrode of Zinc-Air Battery Fuzzy PID Control System Research%锌空电池极片张力PID控制系统研究

    Institute of Scientific and Technical Information of China (English)

    肖艳军; 王旭; 陈宏; 朱瑞峰

    2013-01-01

    锌空电池作为一种高效、无污染和可回收利用能源,成为当今世界电池领域开发的热点,有巨大市场前景.在锌空电池生产线中,张力对保证产品质量有重要的作用.按照张力产生原因不同,对锌空电池极片生产线控制系统进行模糊控制器的设计.以电池极片生产线的张力控制为研究对象,以开卷机构为例,建立张力控制系统的数学模型;并将模糊PID算法应用于张力控制系统中,仿真研究结果表明在控制器中引入模糊PID控制,系统的性能得到了很大的改善,能很好的实现恒张力运行.%As an efficient,no pollution and recycled kind of energy,Zn-air battery is regarded as the hotspot of its field and has market prospects.Tension in zinc-air battery production line plays an important role in ensuring the quality of products.It makes tension control of electrode of zinc-air battery production line as research object.According to the different cause of tension,designing fuzzy controller of the control system.Taking uncoiling mechanism as an example,it establishes a mathematical model of the tension control system; and applies fuzzy PID algorithm to tension control system.Simulation results show that using fuzzy PID control in the controller,the performance of the system gets a big improvement; it can realize controlling of constant tension.

  20. High-intensity ultrasonication as a way to prepare graphene/amorphous iron oxyhydroxide hybrid electrode with high capacity in lithium battery.

    Science.gov (United States)

    González, José R; Menéndez, Rosa; Alcántara, Ricardo; Nacimiento, Francisco; Tirado, José L; Zhecheva, Ekaterina; Stoyanova, Radostina

    2015-05-01

    The preparation of graphene/iron oxyhydroxide hybrid electrode material with very homogeneous distribution and close contact of graphene and amorphous iron oxyhydroxide nanoparticles has been achieved by using high-intensity ultrasonication. Due to the negative charge of the graphene surface, iron ions are attracted toward the surface of dispersed graphene, according to the zeta potential measurements. The anchoring of the FeO(OH) particles to the graphene layers has been revealed by using mainly TEM, XPS and EPR. TEM observations show that the size of the iron oxide particles is about 4 nm. The ultrasonication treatment is the key parameter to achieve small particle size in these graphene/iron oxyhydroxide hybrid materials. The electrochemical behavior of composite graphene/amorphous iron oxyhydroxide prepared by using high-intensity ultrasonication is outstanding in terms of gravimetric capacity and cycling stability, particularly when metallic foam is used as both the substrate and current collector. The XRD-amorphous character of iron oxyhydroxide in the hybrid electrode material and the small particle size contribute to achieve the improved electrochemical performance.