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Sample records for alkaline battery electrodes

  1. A method for making an alkaline battery electrode plate

    NASA Technical Reports Server (NTRS)

    Chida, K.; Ezaki, T.

    1983-01-01

    A method is described for making an alkaline battery electrode plate where the desired active substances are filled into a nickel foam substrate. In this substrate an electrolytic oxidation reduction occurs in an alkaline solution containing lithium hydroxide.

  2. Additive for activating iron electrodes in alkaline batteries

    SciTech Connect

    Berger, G.; Haschka, F.

    1981-02-10

    An additive is disclosed for the iron electrodes of alkaline batteries which prevents and counteracts the tendency of iron electrodes to become passive and ineffective. The additive consists of sulfide, selenide or telluride which is sparingly soluble in the electrolyte and has a decomposition potential more electronegative than the final charging potential of the iron electrode. The additive may be placed in the active electrode material during manufacture but may also be placed in the battery during or after manufacture, for example in tablet form. The additive may also be introduced in a manner permitting subsequent activation by electrochemical methods. A number of examples is presented.

  3. Investigation of electrode materials for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Arcand, G. M.

    1971-01-01

    A number of amalgam electrode systems were investigated for possible use as high rate anodes and cathodes. The systems examined include: lithium, sodium, and potassium in Group 1, magnesium, calcium, and barium in Group 2, aluminum in Group 3, lead in Group 4, copper in Group 1b, and zinc and cadmium in Group 2b. The K(Hg) and Na(Hg) anodes in 10 VF and 15 VF (an unambiguous expression of concentration that indicates the number of formula weights of solute dissolved in a liter of solution) hydroxide solutions have proven satisfactory; some of these have produced current densities of more than 8 A/sq cm. None of the amalgam cathodes have approached this performance although the TI(Hg) has delivered 1 A/sq cm. Se(Hg) and Te(Hg) cathodes have given very stable discharges. Zn(Hg) and Cd(Hg) electrodes did not show good high rate characteristics, 200 to 300 mA/sq cm being about the maximum current densities obtainable. Both anodes are charged through a two-step process in which M(Hg) is first formed electrochemically and subsequently reduces Zn(II or Cd(II) to form the corresponding amalgam. The second step is extremely rapid for zinc and very slow for cadmium.

  4. Development of flexible secondary alkaline battery with carbon nanotube enhanced electrodes

    NASA Astrophysics Data System (ADS)

    Wang, Zhiqian; Mitra, Somenath

    2014-11-01

    We present the development of flexible secondary alkaline battery with rechargeability similar to that of conventional secondary alkaline batteries. Multiwalled carbon nanotubes (MWCNTs) were added to both electrodes to reduce internal resistance, and a cathode containing carbon black and purified MWCNTs was found to be most effective. A polyvinyl alcohol-poly (acrylic acid) copolymer separator served the dual functions of electrolyte storage and enhancing flexibility. Additives to the anode and cathode were effective in reducing capacity fades and improving rechargeability.

  5. Alkaline quinone flow battery.

    PubMed

    Lin, Kaixiang; Chen, Qing; Gerhardt, Michael R; Tong, Liuchuan; Kim, Sang Bok; Eisenach, Louise; Valle, Alvaro W; Hardee, David; Gordon, Roy G; Aziz, Michael J; Marshak, Michael P

    2015-09-25

    Storage of photovoltaic and wind electricity in batteries could solve the mismatch problem between the intermittent supply of these renewable resources and variable demand. Flow batteries permit more economical long-duration discharge than solid-electrode batteries by using liquid electrolytes stored outside of the battery. We report an alkaline flow battery based on redox-active organic molecules that are composed entirely of Earth-abundant elements and are nontoxic, nonflammable, and safe for use in residential and commercial environments. The battery operates efficiently with high power density near room temperature. These results demonstrate the stability and performance of redox-active organic molecules in alkaline flow batteries, potentially enabling cost-effective stationary storage of renewable energy. PMID:26404834

  6. Understanding the Factors Affecting the Formation of Carbonyl Iron Electrodes in Rechargeable Alkaline Iron Batteries

    SciTech Connect

    Manohar, AK; Yang, CG; Malkhandi, S; Yang, B; Prakash, GKS; Narayanan, SR

    2012-01-01

    Rechargeable iron-based alkaline batteries such as iron - air and nickel - iron batteries are attractive for large-scale electrical energy storage because iron is inexpensive, globally-abundant and environmentally-friendly. Further, the iron electrode is known for its robustness to repeated charge/discharge cycling. During manufacturing these batteries are charged and discharged 20 to 50 times during which the discharge capacity of the iron electrode increases gradually and attains a stable value. This process of achieving stable capacity is called formation. In this study we have focused our efforts on understanding the effect of electrode design on formation. We have investigated the role of wetting agent, pore-former additive, and sulfide additive on the formation of carbonyl iron electrodes. The wetting agent increased the rate of formation while the pore-former additive increased the final capacity. Sodium sulfide added to the electrolyte worked as a de-passivation agent and increased the final discharge capacity. We have proposed a phenomenological model for the formation process that predicts the rate of formation and final discharge capacity given the design parameters for the electrode. The understanding gained here will be useful in reducing the time lost in formation and in maximizing the utilization of the iron electrode. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.021301jes] All rights reserved.

  7. Electrodes for sealed secondary batteries

    NASA Technical Reports Server (NTRS)

    Boies, D. B.; Child, F. T.

    1972-01-01

    Self-supporting membrane electrode structures, in which active ingredients and graphite are incorporated in a polymeric matrix, improve performance of electrodes in miniature, sealed, alkaline storage batteries.

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

    NASA Astrophysics Data System (ADS)

    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.

  9. Alkaline battery operational methodology

    DOEpatents

    Sholklapper, Tal; Gallaway, Joshua; Steingart, Daniel; Ingale, Nilesh; Nyce, Michael

    2016-08-16

    Methods of using specific operational charge and discharge parameters to extend the life of alkaline batteries are disclosed. The methods can be used with any commercial primary or secondary alkaline battery, as well as with newer alkaline battery designs, including batteries with flowing electrolyte. The methods include cycling batteries within a narrow operating voltage window, with minimum and maximum cut-off voltages that are set based on battery characteristics and environmental conditions. The narrow voltage window decreases available capacity but allows the batteries to be cycled for hundreds or thousands of times.

  10. Enhancing the Performance of the Rechargeable Iron Electrode in Alkaline Batteries with Bismuth Oxide and Iron Sulfide Additives

    SciTech Connect

    Manohar, AK; Yang, CG; Malkhandi, S; Prakash, GKS; Narayanan, SR

    2013-09-07

    Iron-based alkaline rechargeable batteries have the potential of meeting the needs of large-scale electrical energy storage because of their low-cost, robustness and eco-friendliness. However, the widespread commercial deployment of iron-based batteries has been limited by the low charging efficiency and the poor discharge rate capability of the iron electrode. In this study, we have demonstrated iron electrodes containing bismuth oxide and iron sulfide with a charging efficiency of 92% and capable of being discharged at the 3C rate. Such a high value of charging efficiency combined with the ability to discharge at high rates is being reported for the first time. The bismuth oxide additive led to the in situ formation of elemental bismuth and a consequent increase in the overpotential for the hydrogen evolution reaction leading to an increase in the charging efficiency. We observed that the sulfide ions added to the electrolyte and iron sulfide added to the electrode mitigated-electrode passivation and allowed for continuous discharge at high rates. At the 3C discharge rate, a utilization of 0.2 Ah/g was achieved. The performance level of the rechargeable iron electrode demonstrated here is attractive for designing economically-viable large-scale energy storage systems based on alkaline nickel-iron and iron-air batteries. (C) 2013 The Electrochemical Society. All rights reserved.

  11. Alkaline battery, separator therefore

    NASA Technical Reports Server (NTRS)

    Schmidt, George F. (Inventor)

    1980-01-01

    An improved battery separator for alkaline battery cells has low resistance to electrolyte ion transfer and high resistance to electrode ion transfer. The separator is formed by applying an improved coating to an electrolyte absorber. The absorber, preferably, is a flexible, fibrous, and porous substrate that is resistant to strong alkali and oxidation. The coating composition includes an admixture of a polymeric binder, a hydrolyzable polymeric ester and inert fillers. The coating composition is substantially free of reactive fillers and plasticizers commonly employed as porosity promoting agents in separator coatings. When the separator is immersed in electrolyte, the polymeric ester of the film coating reacts with the electrolyte forming a salt and an alcohol. The alcohol goes into solution with the electrolyte while the salt imbibes electrolyte into the coating composition. When the salt is formed, it expands the polymeric chains of the binder to provide a film coating substantially permeable to electrolyte ion transfer but relatively impermeable to electrode ion transfer during use.

  12. Bifunctional alkaline oxygen electrodes

    NASA Technical Reports Server (NTRS)

    Swette, L.; Kackley, N.; Mccatty, S. A.

    1991-01-01

    The authors describe the identification and testing of electrocatalysts and supports for the positive electrode of moderate-temperature, single-unit, rechargeable alkaline fuel cells. Recent work on Na(x)Pt3O4, a potential bifunctional catalyst, is described, as well as the application of novel approaches to the development of more efficient bifunctional electrode structures. The three dual-character electrodes considered here showed similar superior performance; the Pt/RhO2 and Rh/RhO2 electrodes showed slightly better performance than the Pt/IrO2 electrode. It is concluded that Na(x)Pt3O4 continues to be a promising bifunctional oxygen electrode catalyst but requires further investigation and development.

  13. Modified carbon-free silver electrodes for the use as cathodes in lithium-air batteries with an aqueous alkaline electrolyte

    NASA Astrophysics Data System (ADS)

    Wittmaier, Dennis; Wagner, Norbert; Friedrich, K. Andreas; Amin, Hatem M. A.; Baltruschat, Helmut

    2014-11-01

    Gas diffusion electrodes with silver catalysts show a high activity towards oxygen reduction reaction in alkaline media but a rather poor activity towards oxygen evolution reaction. For the use in future lithium-air batteries with an aqueous alkaline electrolyte the activity of such electrodes must be improved significantly. As Co3O4 is a promising metal oxide catalyst for oxygen evolution in alkaline media, silver electrodes were modified with Co3O4. For comparison silver electrodes were also modified with IrO2. Due to the poor stability of carbon materials at high anodic potentials these gas diffusion electrodes were prepared without carbon support to improve especially the long-term stability. Gas diffusion electrodes were electrochemically investigated in an electrochemical half-cell arrangement. In addition to cyclic voltammograms electrochemical impedance spectroscopy (EIS) was carried out. SEM and XRD were used for the physical and morphological investigations. Investigations showed that silver electrodes containing 20 wt.% Co3O4 exhibited the highest performance and highest long-term stability. For comparison, rotating - ring - disc - electrode experiments have been performed using model electrodes with thin catalyst layers, showing that the amount of hydrogen peroxide evolved is negligible.

  14. Inorganic-organic separators for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W. (Inventor)

    1978-01-01

    A flexible separator is reported for use between the electrodes of Ni-Cd and Ni-Zn batteries using alkaline electrolytes. The separator was made by coating a porous substrate with a battery separator composition. The coating material included a rubber-based resin copolymer, a plasticizer and inorganic and organic fillers which comprised 55% by volume or less of the coating as finally dried. One or more of the filler materials, whether organic or inorganic, is preferably active with the alkaline electrolyte to produce pores in the separator coating. The plasticizer was an organic material which is hydrolyzed by the alkaline electrolyte to improve conductivity of the separator coating.

  15. Improved zinc electrode and rechargeable zinc-air battery

    SciTech Connect

    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.

  16. Rechargeable Zn-MnO sub 2 alkaline batteries

    SciTech Connect

    Wruck, W.J.; Reichman, B.; Bullock, K.R.; Kao, W.H. )

    1991-12-01

    In this paper progress in the development of rechargeable alkaline zinc-manganese dioxide cells is described. The advantages and limitations of the system are evaluated. Laboratory tests run on commercial primary alkaline cells as well as model simulations of a bipolar MnO{sub 2} electrode show that the rechargeable alkaline battery may be able to compete with lead-acid, nickel-cadmium, and secondary lithium cells for low- to moderate-rate applications. However, because of this poor performance at high rates and low temperatures, the alkaline MnO{sub 2} battery is not suitable for present automotive starting applications.

  17. Flexible separator for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.

    1977-01-01

    Device is fabricated from low-cost readily-available commercial-materials by automated methods utilizing conventional paper coating processes. Flexibility of unit prevents cracking and disintegration caused by electrode warpage and dendrite growth, major causes of early battery failure with present separators.

  18. Battery electrode growth accommodation

    DOEpatents

    Bowen, Gerald K.; Andrew, Michael G.; Eskra, Michael D.

    1992-01-01

    An electrode for a lead acid flow through battery, the grids including a plastic frame, a plate suspended from the top of the frame to hang freely in the plastic frame and a paste applied to the plate, the paste being free to allow for expansion in the planar direction of the grid.

  19. Grace DAKASEP alkaline battery separator

    NASA Technical Reports Server (NTRS)

    Giovannoni, R. T.; Lundquist, J. T.; Choi, W. M.

    1987-01-01

    The Grace DAKASEP separator was originally developed as a wicking layer for nickel-zinc alkaline batteries. The DAKASEP is a filled non-woven separator which is flexible and heat sealable. Through modification of formulation and processing variables, products with a variety of properties can be produced. Variations of DAKASEP were tested in Ni-H2, Ni-Zn, Ni-Cd, and primary alkaline batteries with good results. The properties of DAKASEP which are optimized for Hg-Zn primary batteries are shown in tabular form. This separator has high tensile strength, 12 micron average pore size, relatively low porosity at 46-48 percent, and consequently moderately high resistivity. Versions were produced with greater than 70 percent porosity and resistivities in 33 wt percent KOH as low as 3 ohm cm. Performance data for Hg-Zn E-1 size cells containing DAKASEP with the properties shown in tabular form, are more reproducible than data obtained with a competitive polypropylene non-woven separator. In addition, utilization of active material is in general considerably improved.

  20. Assembly and electrochemical properties of novel alkaline rechargeable Ni/Bi battery using Ni(OH)2 and (BiO)4CO3(OH)2 microspheres as electrode materials

    NASA Astrophysics Data System (ADS)

    Sun, Jinfeng; Wang, Jinqing; Li, Zhangpeng; Niu, Lengyuan; Hong, Wei; Yang, Shengrong

    2015-01-01

    In this work, Ni(OH)2 and (BiO)4CO3(OH)2 microspheres are synthesized by solvothermal method. Then, a novel alkaline rechargeable Ni/Bi battery is assembled for the first time using the synthesized Ni(OH)2 and (BiO)4CO3(OH)2 as the positive electrode and negative electrode materials, respectively. As a result, the assembled Ni/Bi battery delivers a high specific capacity of 113 mAh g-1 at a discharge rate of 0.2C based on the total mass of the electrode materials, as well as a high energy density of 92 Wh kg-1 at a power density of 27.3 W kg-1.

  1. Polyvinyl alcohol battery separator containing inert filler. [alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Hsu, L. C.; Manzo, M. A. (Inventor)

    1981-01-01

    A cross-linked polyvinyl alcohol battery separator is disclosed. A particulate filler, inert to alkaline electrolyte of an alkaline battery, is incorporated in the separator in an amount of 1-20% by weight, based on the weight of the polyvinyl alcohol, and is dispersed throughout the product. Incorporation of the filler enhances performance and increases cycle life of alkaline batteries when compared with batteries containing a similar separator not containing filler. Suitable fillers include titanates, silicates, zirconates, aluminates, wood floor, lignin, and titania. Particle size is not greater than about 50 microns.

  2. Composite seal reduces alkaline battery leakage

    NASA Technical Reports Server (NTRS)

    Clatterbuck, C. H.; Plitt, K. F.

    1965-01-01

    Composite seal consisting of rubber or plastic washers and a metal washer reduces alkaline battery leakage. Adhesive is applied to each washer interface, and the washers are held together mechanically.

  3. Zinc electrode and rechargeable zinc-air battery

    DOEpatents

    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.

  4. Positive Active Material For Alkaline Electrolyte Storage Battert Nickel Electrodes

    DOEpatents

    Bernard, Patrick; Baudry, Michelle

    2000-12-05

    A method of manufacturing a positive active material for nickel electrodes of alkaline storage batteries which consists of particles of hydroxide containing mainly nickel and covered with a layer of a hydroxide phase based on nickel and yttrium is disclosed. The proportion of the hydroxide phase is in the range 0.15% to 3% by weight of yttrium expressed as yttrium hydroxide relative to the total weight of particles.

  5. A universial gas absorber for sealed alkaline storage batteries

    SciTech Connect

    Tsenter, B.I.; Laurenov, V.M.

    1986-02-01

    The authors describe a universal gas absorber for all types of sealed alkaline storage batteries. The absorber is illustrated and consists of matrix-type nickel-gas cells which are connected in series, have a common gas compartment, and are electrolytically insulated from each other. The gas electrode of the nickel gas cell is bifunctional; it functions in oxygen ionization and in hydrogen ionization. The solid-phase nickel-oxide electrode is a powder-metallurgical design. Absorbers of the present type are universal, both in the sense that they will absorb oxygen, hydrogen, or a mixture of these gases, and in the sense that they can be used for sealed alkaline storage batteries of any type.

  6. Zinc electrode and rechargeable zinc-air battery

    SciTech Connect

    Ross, P.N. Jr.

    1989-06-27

    This patent describes an improved zinc electrode 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.

  7. Negative Electrode For An Alkaline Cell

    DOEpatents

    Coco, Isabelle; Cocciantelli, Jean-Michel; Villenave, Jean-Jacques

    1998-07-14

    The present invention concerns a negative electrode for an alkaline cell, comprising a current collector supporting a paste containing an electrochemically active material and a binder, characterized in that said binder is a polymer containing hydrophilic and hydrophobic groups, said polymer being selected from an acrylic homopolymer, copolymer and terpolymer, an unsaturated organic acid copolymer and an unsaturated acid anhydride copolymer.

  8. Fundamental principals of battery design: Porous electrodes

    NASA Astrophysics Data System (ADS)

    Qu, Deyang

    2014-06-01

    The fundamental aspects of a porous electrode from electrochemistry and material chemistry standpoints are discussed in the light of battery engineering designs. For example, the ionic diffusion, the electrode-electrolyte interface, interfacial charge transfer and electrode catalytic processes are discussed. The discussion of such fundamental electrochemical aspects is in conjunction with the design of batteries, e.g. the electrochemical assessable surface area for porous electrode, electrode catalytic reactions. The porous electrodes used as a gas diffusion electrode and the electrode in a supercapacitor are discussed to demonstrate the application of electrochemical principals in battery design.

  9. Batteries: from alkaline to zinc-air.

    PubMed

    Dondelinger, Robert M

    2004-01-01

    There is no perfect disposable battery--one that will sit on the shelf for 20 years, then continually provide unlimited current, at a completely constant voltage until exhausted, without producing heat. There is no perfect rechargeable battery--one with all of the above characteristics and will also withstand an infinite overcharge while providing an equally infinite cycle life. There are only compromises. Every battery selection is a compromise between the ideally required characteristics, the advantages, and the limitations of each battery type. General selection of a battery type to power a medical device is largely outside the purview of the biomed. Initially, these are engineering decisions made at the time of medical equipment design and are intended to be followed in perpetuity. However, since newer cell types evolve and the manufacturer's literature is fixed at the time of printing, some intelligent substitutions may be made as long as the biomed understands the characteristics of both the recommended cell and the replacement cell. For example, when the manufacturer recommends alkaline, it is usually because of the almost constant voltage it produces under the devices' design load. Over time, other battery types may be developed that will meet the intent of the manufacturer, at a lower cost, providing longer operational life, at a lower environmental cost, or with a combination of these advantages. In the Obstetrical Doppler cited at the beginning of this article, the user had put in carbon-zinc cells, and the biomed had unknowingly replaced them with carbonzinc cells. If the alkaline cells recommended by the manufacturer had been used, there would have been the proper output voltage at the battery terminals when the [table: see text] cells were at their half-life. Instead, the device refused to operate since the battery voltage was below presumed design voltage. While battery-type substitutions may be easily and relatively successfully made in disposable

  10. Oxygen electrodes for rechargeable alkaline fuel cells

    NASA Technical Reports Server (NTRS)

    Swette, Larry; Giner, Jose

    1987-01-01

    Electrocatalysts and supports for the positive electrode of moderate temperature single unit rechargeable alkaline fuel cells were investigated and developed. The electrocatalysts are defined as the material with a higher activity for the oxygen electrode reaction than the support. Advanced development will require that the materials be prepared in high surface area forms, and may also entail integration of various candidate materials. Eight candidate support materials and seven electrocatalysts were investigated. Of the 8 support, 3 materials meet the preliminary requirements in terms of electrical conductivity and stability. Emphasis is now on preparing in high surface area form and testing under more severe corrosion stress conditions. Of the 7 electrocatalysts prepared and evaluated, at least 5 materials remain as potential candidates. The major emphasis remains on preparation, physical characterization and electrochemical performance testing.

  11. Advanced inorganic separators for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W. (Inventor)

    1982-01-01

    A flexible, porous battery separator comprising a coating applied to a porous, flexible substrate is described. The coating comprises: (1) a thermoplastic rubber-based resin which is insoluble and unreactive in the alkaline electrolyte; (2) a polar organic plasticizer which is reactive with the alkaline electrolyte to produce a reaction product which contains a hydroxyl group and/or a carboxylic acid group; and (3) a mixture of polar particulate filler materials which are unreactive with the electrolyte, the mixture comprising at least one first filler material having a surface area of greater than 25 meters sq/gram, at least one second filler material having a surface area of 10 to 25 sq meters/gram, wherein the volume of the mixture of filler materials is less than 45% of the total volume of the fillers and the binder, the filler surface area per gram of binder is about 20 to 60 sq meters/gram, and the amount of plasticizer is sufficient to coat each filler particle. A method of forming the battery separator is also described.

  12. Fabrication of high-performance flexible alkaline batteries by implementing multiwalled carbon nanotubes and copolymer separator.

    PubMed

    Wang, Zhiqian; Wu, Zheqiong; Bramnik, Natalia; Mitra, Somenath

    2014-02-12

    A flexible alkaline battery with multiwalled carbon nanotube (MWCNT) enhanced composite electrodes and polyvinyl alcohol (PVA)-poly (acrylic acid) (PAA) copolymer separator has been developed. Purified MWCNTs appear to be the most effective conductive additive, while the flexible copolymer separator not only enhances flexibility but also serves as electrolyte storage. PMID:24510667

  13. Oxygen electrodes for rechargeable alkaline fuel cells

    NASA Technical Reports Server (NTRS)

    Swette, L.; Kackley, N.

    1989-01-01

    Electrocatalysts and supports for the positive electrode of moderate temperature single-unit rechargeable alkaline fuel cells are being investigated and developed. Candidate support materials were drawn from transition metal carbides, borides, nitrides and oxides which have high conductivity (greater than 1 ohm/cm). Candidate catalyst materials were selected largely from metal oxides of the form ABO sub x (where A = Pb, Cd, Mn, Ti, Zr, La, Sr, Na, and B = Pt, Pd, Ir, Ru, Ni (Co) which were investigated and/or developed for one function only, O2 reduction or O2 evolution. The electrical conductivity requirement for catalysts may be lower, especially if integrated with a higher conductivity support. All candidate materials of acceptable conductivity are subjected to corrosion testing. Materials that survive chemical testing are examined for electrochemical corrosion activity. For more stringent corrosion testing, and for further evaluation of electrocatalysts (which generally show significant O2 evolution at at 1.4 V), samples are held at 1.6 V or 0.6 V for about 100 hours. The surviving materials are then physically and chemically analyzed for signs of degradation. To evaluate the bifunctional oxygen activity of candidate catalysts, Teflon-bonded electrodes are fabricated and tested in a floating electrode configuration. Many of the experimental materials being studied have required development of a customized electrode fabrication procedure. In advanced development, the goal is to reduce the polarization to about 300 to 350 mV. Approximately six support materials and five catalyst materials were identified to date for further development. The test results will be described.

  14. Polyvinyl alcohol membranes as alkaline battery separators

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Gonzalez-Sanabria, O.; Manzo, M. A.

    1982-01-01

    Polyvinly alcohol (PVA) cross-linked with aldehyde reagents yields membranes that demonstrate properties that make them suitable for use as alkaline battery separators. Film properties can be controlled by the choice of cross-linker, cross-link density and the method of cross-linking. Three methods of cross-linking and their effects on film properties are discussed. Film properties can also be modified by using a copolymer of vinyl alcohol and acrylic acid as the base for the separator and cross-linking it similarly to the PVA. Fillers can be incorporated into the films to further modify film properties. Results of separator screening tests and cell tests for several variations of PBA films are discussed.

  15. Diffusion induced stresses in buckling battery electrodes

    NASA Astrophysics Data System (ADS)

    Bhandakkar, Tanmay K.; Johnson, Harley T.

    2012-06-01

    Highly networked nanostructured battery electrode materials offer the possibility of achieving both rapid battery charge-discharge rates and high storage capacity. Recently, lithium ion battery (LIB) electrodes based on a 2-D honeycomb architecture were shown to undergo remarkable and reversible morphological changes during the lithiation process. Charge-discharge rates in 3-D composite electrode have also been shown to benefit from sandwiching the electrolytically active material between highly conductive ion and electron transport pathways to reduce electrical resistance and solid-state diffusion lengths. In the present work we simulate and analyze the observed morphological changes in honeycomb electrodes, with and without the presence of conductive pathways, during the lithiation-delithiation process. Diffusion induced stresses are analyzed for such structures undergoing elastic-plastic deformation during cycling. The results show that such a periodic, nanostructured electrode geometry allows for the presence of buckling-like deformation modes, which effectively reduce the resulting mechanical stresses that lead to electrode failure.

  16. Separator for alkaline batteries and method of making same

    NASA Technical Reports Server (NTRS)

    Hoyt, H. E.; Pfluger, H. L. (Inventor)

    1970-01-01

    The preparation of membranes suitable for use as separators in concentrated alkaline battery cells by selective solvolysis of copolymers of methacrylate esters with acrylate esters followed by addition of a base and to the resultant products is described. The method of making copolymers by first copolymerizing a methacrylate ester (or esters) with a more readily hydrolyzable ester, followed by a selective saponification whereby the methacrylate ester moieties remain essentially intact and the readily hydrolyzable ester moiety is suponified and to the partial or complete neutralization of the relatively brittle copolymer acid with a base to make membranes which are sufficiently flexible in the dry state so that they may be wrapped around electrodes without damage by handling is described.

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

    NASA Astrophysics Data System (ADS)

    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.

  18. A facile chemical route for recovery of high quality zinc oxide nanoparticles from spent alkaline batteries.

    PubMed

    Deep, Akash; Sharma, Amit L; Mohanta, Girish C; Kumar, Parveen; Kim, Ki-Hyun

    2016-05-01

    Recycling of spent domestic batteries has gained a great environmental significance. In the present research, we propose a new and simple technique for the recovery of high-purity zinc oxide nanoparticles from the electrode waste of spent alkaline Zn-MnO2 batteries. The electrode material was collected by the manual dismantling and mixed with 5M HCl for reaction with a phosphine oxide reagent Cyanex 923® at 250°C for 30min. The desired ZnO nanoparticles were restored from the Zn-Cyanex 923 complex through an ethanolic precipitation step. The recovered particle product with about 5nm diameter exhibited fluorescent properties (emission peak at 400nm) when excited by UV radiation (excitation energy of 300nm). Thus, the proposed technique offered a simple and efficient route for recovering high purity ZnO nanoparticles from spent alkaline batteries. PMID:26851168

  19. Negative Electrodes for Li-Ion Batteries

    SciTech Connect

    Kinoshita, Kim; Zaghib, Karim

    2001-10-01

    Graphitized carbons have played a key role in the successful commercialization of Li-ion batteries. The physicochemical properties of carbon cover a wide range; therefore identifying the optimum active electrode material can be time consuming. The significant physical properties of negative electrodes for Li-ion batteries are summarized, and the relationship of these properties to their electrochemical performance in nonaqueous electrolytes, are discussed in this paper.

  20. Silver manganese oxide electrodes for lithium batteries

    DOEpatents

    Thackeray, Michael M.; Vaughey, John T.; Dees, Dennis W.

    2006-05-09

    This invention relates to electrodes for non-aqueous lithium cells and batteries with silver manganese oxide positive electrodes, denoted AgxMnOy, in which x and y are such that the manganese ions in the charged or partially charged electrodes cells have an average oxidation state greater than 3.5. The silver manganese oxide electrodes optionally contain silver powder and/or silver foil to assist in current collection at the electrodes and to improve the power capability of the cells or batteries. The invention relates also to a method for preparing AgxMnOy electrodes by decomposition of a permanganate salt, such as AgMnO4, or by the decomposition of KMnO4 or LiMnO4 in the presence of a silver salt.

  1. Long life lithium batteries with stabilized electrodes

    DOEpatents

    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.

  2. Redox polymer electrodes for advanced batteries

    DOEpatents

    Gregg, Brian A.; Taylor, A. Michael

    1998-01-01

    Advanced batteries having a long cycle lifetime are provided. More specifically, the present invention relates to electrodes made from redox polymer films and batteries in which either the positive electrode, the negative electrode, or both, comprise redox polymers. Suitable redox polymers for this purpose include pyridyl or polypyridyl complexes of transition metals like iron, ruthenium, osmium, chromium, tungsten and nickel; porphyrins (either free base or metallo derivatives); phthalocyanines (either free base or metallo derivatives); metal complexes of cyclams, such as tetraazacyclotetradecane; metal complexes of crown ethers and metallocenes such as ferrocene, cobaltocene and ruthenocene.

  3. Redox polymer electrodes for advanced batteries

    DOEpatents

    Gregg, B.A.; Taylor, A.M.

    1998-11-24

    Advanced batteries having a long cycle lifetime are provided. More specifically, the present invention relates to electrodes made from redox polymer films and batteries in which either the positive electrode, the negative electrode, or both, comprise redox polymers. Suitable redox polymers for this purpose include pyridyl or polypyridyl complexes of transition metals like iron, ruthenium, osmium, chromium, tungsten and nickel; porphyrins (either free base or metallo derivatives); phthalocyanines (either free base or metallo derivatives); metal complexes of cyclams, such as tetraazacyclotetradecane; metal complexes of crown ethers and metallocenes such as ferrocene, cobaltocene and ruthenocene. 2 figs.

  4. Light Weight Design Nickel-Alkaline Cells Using Fiber Electrodes

    NASA Technical Reports Server (NTRS)

    Pickett, David F.; Willis, Bob; Britton, Doris; Saelens, Johan

    2005-01-01

    Using fiber electrode technology, currently produced by Bekaert Corporation (Bekaert), Electro Energy, Inc., (EEI) Mobile Energy Products Group (formerly, Eagle-Picher Technologies, LLC., Power Systems Department) in Colorado Springs, CO has demonstrated that it is feasible to manufacture flight weight nickel-hydrogen cells having about twice the specific energy (80 vs. 40 watt-hr/kg) as state-of-the-art nickel-hydrogen cells that are flown on geosynchronous communications satellites. Although lithium-ion battery technology has made large in-roads to replace the nickel-alkaline technology (nickel-cadmium, nickel-metal hydride), the technology offered here competes with lithium-ion weight and offers alternatives not present in the lithium-ion chemistry such as ability to undergo continuous overcharge, reversal on discharge and sustain rate capability sufficient to start automotive and aircraft engines at subzero temperatures. In development to date seven 50 ampere-hour nickel-hydrogen have been constructed, acceptance tested and briefly tested in a low earth orbit (LEO) cycle regime. The effort was jointly funded by Electro Energy, Inc. and NASA Glenn Research Center, Cleveland, OH. Five of the seven cells have been shipped to NASA GRC for further cycle testing. Two of the cells experienced failure due to internal short circuits during initial cycle testing at EEL Destructive Physical Analysis (DPA) of one of the cells has shown the failure mode to be due to inadequate hydrogen catalyst electrodes that were not capacity balanced with the higher energy density nickel oxide electrodes. In the investigators opinion, rebuild of the cells using proper electrode balance would result in cells that could sustain over 30,000 cycles at moderate depths-of-discharge in a LEO regime or endure over 20 years of geosynchronous orbit (GEO) cycling while realizing a two-fold increase in specific energy for the battery or a 1.1 kg weight savings per 50 ampere-hour cell. Additional

  5. Negative electrodes for lithium cells and batteries

    DOEpatents

    Vaughey, John T.; Fransson, Linda M.; Thackeray, Michael M.

    2005-02-15

    A negative electrode is disclosed for a non-aqueous electrochemical cell. The electrode has an intermetallic compound as its basic structural unit with the formula M.sub.2 M' in which M and M' are selected from two or more metal elements including Si, and the M.sub.2 M' structure is a Cu.sub.2 Sb-type structure. Preferably M is Cu, Mn and/or Li, and M' is Sb. Also disclosed is a non-aqueous electrochemical cell having a negative electrode of the type described, an electrolyte and a positive electrode. A plurality of cells may be arranged to form a battery.

  6. Oxygen electrodes for rechargeable alkaline fuel cells, 3

    NASA Technical Reports Server (NTRS)

    Swette, L.; Kackley, N.; Mccatty, S. A.

    1991-01-01

    The investigation and development of electrocatalysts and supports for the positive electrode of moderate temperature single unit rechargeable alkaline fuel cells is described. Focus is on chemical and electrochemical stability and O2 reduction/evolution activity of the electrode in question.

  7. Polymeric metallic electrodes for rechargeable battery applications

    NASA Technical Reports Server (NTRS)

    Somoano, R.

    1982-01-01

    A review is presented on the status of plastic metal electrodes, emphasizing the use of polyacetylene as a prototype polymeric material. The electrochemical characteristics of polyacetylene are examined; and the potential use of this material, as well as other types of plastic metal electrodes, in batteries is evaluated. Several problem areas which must be solved before polyacetylene can be widely used in battery applications are discussed, including the problem of electrolyte stability, the problem that the depth of discharge and the energy density is limited by the metal-semiconductor transition, and also the poor electrochemical performance of impure material.

  8. Separator Materials Used in Secondary Alkaline Batteries Characterized and Evaluated

    NASA Technical Reports Server (NTRS)

    1996-01-01

    Nickel-cadmium (Ni/Cd) and nickel-hydrogen (Ni/H2) secondary alkaline batteries are vital to aerospace applications. Battery performance and cycle life are significantly affected by the type of separators used in those batteries. A team from NASA Lewis Research Center's Electrochemical Technology Branch developed standardized testing procedures to characterize and evaluate new and existing separator materials to improve performance and cycle life of secondary alkaline batteries. Battery separators must function as good electronic insulators and as efficient electrolyte reservoirs. At present, new types of organic and inorganic separator materials are being developed for Ni/Cd and Ni/H2 batteries. The separator material previously used in the NASA standard Ni/Cd was Pellon 2505, a 100-percent nylon-6 polymer that must be treated with zinc chloride (ZnCl2) to bond the fibers. Because of stricter Environmental Protection Agency regulation of ZnCl2 emissions, the battery community has been searching for new separators to replace Pellon 2505. As of today, two candidate separator materials have been identified; however, neither of the two materials have performed as well as Pellon 2505. The separator test procedures that were devised at Lewis are being implemented to expedite the search for new battery separators. The new test procedures, which are being carried out in the Separator Laboratory at Lewis, have been designed to guarantee accurate evaluations of the properties that are critical for sustaining proper battery operation. These properties include physical and chemical stability, chemical purity, gas permeability, electrolyte retention and distribution, uniformity, porosity, and area resistivity. A manual containing a detailed description of 12 separator test procedures has been drafted and will be used by the battery community to evaluate candidate separator materials for specific applications. These standardized procedures will allow for consistent, uniform

  9. Stability in alkaline aqueous electrolyte of air electrode protected with fluorinated interpenetrating polymer network membrane

    NASA Astrophysics Data System (ADS)

    Bertolotti, Bruno; Messaoudi, Houssam; Chikh, Linda; Vancaeyzeele, Cédric; Alfonsi, Séverine; Fichet, Odile

    2015-01-01

    We developed original anion exchange membranes to protect air electrodes operating in aqueous lithium-air battery configuration, i.e. supplied with atmospheric air and in concentrated aqueous lithium hydroxide. These protective membranes have an interpenetrating polymer network (IPN) architecture combining a hydrogenated cationic polyelectrolyte network based on poly(epichlorohydrin) (PECH) and a fluorinated neutral network based on perfluoropolyether (Fluorolink® MD700). Two phases, each one rich in one of the polymer, are co-continuous in the materials. This morphology allows combining their properties according to the weight proportions of each polymer. Thus, PECH/Fluorolink IPNs show ionic conductivity varying from 1 to 2 mS cm-1, water uptake from 30 to 90 wt.% and anionic transport number from 0.65 to 0.80 when the PECH proportion varies from 40 to 90 wt.%. These membranes have been systematically assembled on air electrodes. Air electrode protected with PECH/Fluorolink 70/30 IPN shows outstanding stability higher than 1000 h, i.e. a 20-fold increase in the lifetime of the non-modified electrode. This efficient membrane/air electrode assembly is promising for development of alkaline electrolyte based storage or production energy systems, such as metal air batteries or alkaline fuel cells.

  10. Performance of alkaline battery cells used in emergency locator transmitters

    NASA Technical Reports Server (NTRS)

    Haynes, G. A.; Sokol, S.; Motley, W. R., III; Mcclelland, E. L.

    1984-01-01

    The characteristics of battery power supplies for emergency locator transmitters (ELT's) were investigated by testing alkaline zinc/manganese dioxide cells of the type typically used in ELT's. Cells from four manufacturers were tested. The cells were subjected to simulated environmental and load conditions representative of those required for survival and operation. Battery cell characteristics that may contribute to ELT malfunctions and limitations were evaluated. Experimental results from the battery cell study are discussed, and an evaluation of ELT performance while operating under a representative worst-case environmental condition is presented.

  11. Lithium battery electrodes with ultra-thin alumina coatings

    SciTech Connect

    Se-Hee, Lee; George, Steven M.; Cavanagh, Andrew S.; Yoon Seok, Jung; Dillon, Anne C.

    2015-11-24

    Electrodes for lithium batteries are coated via an atomic layer deposition process. The coatings can be applied to the assembled electrodes, or in some cases to particles of electrode material prior to assembling the particles into an electrode. The coatings can be as thin as 2 .ANG.ngstroms thick. The coating provides for a stable electrode. Batteries containing the electrodes tend to exhibit high cycling capacities.

  12. Manganese oxide composite electrodes for lithium batteries

    DOEpatents

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

    2009-12-22

    An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor thereof a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0.5electrode and 0.ltoreq.y<1 in which the Li.sub.2MnO.sub.3 and LiMn.sub.2-yM.sub.yO.sub.4 components have layered and spinel-type structures, respectively, and in which M is one or more metal cations. The electrode is activated by removing lithia, or lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

  13. Oxygen electrodes for rechargeable alkaline fuel cells. II

    NASA Technical Reports Server (NTRS)

    Swette, L.; Kackley, N.

    1990-01-01

    The primary objective of this program is the investigation and development of electrocatalysts and supports for the positive electrode of moderate temperature, single-unit, rechargeable alkaline fuel cells. Approximately six support materials and five catalyst materials have been identified to date for further development.

  14. Oxygen electrodes for rechargeable alkaline fuel cells-II

    NASA Technical Reports Server (NTRS)

    Swette, L.; Kackley, N.

    1989-01-01

    The primary objective of this program is the investigation and development of electrocatalysts and supports for the positive electrode of moderate temperature single-unit rechargeable alkaline fuel cells. Approximately six support materials and five catalyst materials have been identified to date for further development.

  15. Nickel hydrogen bipolar battery electrode design

    NASA Technical Reports Server (NTRS)

    Puglisi, V. J.; Russell, P.; Verrier, D.; Hall, A.

    1985-01-01

    The preferred approach of the NASA development effort in nickel hydrogen battery design utilizes a bipolar plate stacking arrangement to obtain the required voltage-capacity configuration. In a bipolar stack, component designs must take into account not only the typical design considerations such as voltage, capacity and gas management, but also conductivity to the bipolar (i.e., intercell) plate. The nickel and hydrogen electrode development specifically relevant to bipolar cell operation is discussed. Nickel oxide electrodes, having variable type grids and in thicknesses up to .085 inch are being fabricated and characterized to provide a data base. A selection will be made based upon a system level tradeoff. Negative (hydrpogen) electrodes are being screened to select a high performance electrode which can function as a bipolar electrode. Present nickel hydrogen negative electrodes are not capable of conducting current through their cross-section. An electrode was tested which exhibits low charge and discharge polarization voltages and at the same time is conductive. Test data is presented.

  16. Electrodeposited inorganic separators for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Carson, W. N., Jr.; Consiglio, J. A.; Mc Quade, J. M.

    1970-01-01

    Coating electrodes of silver-cadmium cells with thermostable electrodeposits of calcium hydroxide or magnesium hydroxide reduces silver migration and increases cell life. Absence of organic matter enables assembled cells to be sterilized without oxidation of the material of the separators.

  17. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

    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.x<1 and .delta. is less than 0.2, and in which M is a non-lithium 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. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

  18. Manganese oxide composite electrodes for lithium batteries

    DOEpatents

    Thackeray, Michael M.; Johnson, Christopher S.; Li, Naichao

    2007-12-04

    An activated electrode for a non-aqueous electrochemical cell is disclosed with a precursor of a lithium metal oxide with the formula xLi.sub.2MnO.sub.3.(1-x)LiMn.sub.2-yM.sub.yO.sub.4 for 0electrode is activated by removing lithia, or lithium and lithia, from the precursor. A cell and battery are also disclosed incorporating the disclosed positive electrode.

  19. Life capability of the silver electrode in alkaline electrochemical cells

    NASA Technical Reports Server (NTRS)

    Frank, H. A.

    1976-01-01

    Estimates of silver electrode degradation rates were made by comparing the recently measured capacities with the reported early life capacities. Chemical analyses were carried out to determine the extent of silver loss from the electrode and its distribution throughout the cell components. The results established that the silver electrode is very stable when stored at reduced temperatures in the range of 0 to -51 C, in which it exhibits a permanent degradation in capacity of 0.5%/year. The results also indicated that the silver electrode is not quite as stable when operated and stored at room temperature, where it exhibits permanent degradation in the range of 3% to 14%/year. These results were employed in predicting the life capability of the proposed new Ag-H2 cell and also in assessing the merits of employing silver electrodes in long-life probe batteries.

  20. Aqueous Rechargeable Alkaline CoxNi2-xS2/TiO2 Battery.

    PubMed

    Liu, Jilei; Wang, Jin; Ku, Zhiliang; Wang, Huanhuan; Chen, Shi; Zhang, Lili; Lin, Jianyi; Shen, Ze Xiang

    2016-01-26

    An electrochemical energy storage system with high energy density, stringent safety, and reliability is highly desirable for next-generation energy storage devices. Here an aqueous rechargeable alkaline CoxNi2-xS2 // TiO2 battery system is designed by integrating two reversible electrode processes associated with OH(-) insertion/extraction in the cathode part and Li ion insertion/extraction in the anode part, respectively. The prototype CoxNi2-xS2 // TiO2 battery is able to deliver high energy/power densities of 83.7 Wh/kg at 609 W/kg (based on the total mass of active materials) and good cycling stabilities (capacity retention 75.2% after 1000 charge/discharge cycles). A maximum volumetric energy density of 21 Wh/l (based on the whole packaged cell) has been achieved, which is comparable to that of a thin-film battery and better than that of typical commercial supercapacitors, benefiting from the unique battery and hierarchical electrode design. This hybrid system would enrich the existing aqueous rechargeable LIB chemistry and be a promising battery technology for large-scale energy storage. PMID:26593375

  1. Solvent processible, high-performance partially fluorinated copoly(arylene ether) alkaline ionomers for alkaline electrodes

    NASA Astrophysics Data System (ADS)

    Zhou, Junfeng; Ünlü, Murat; Anestis-Richard, Irene; Kim, Hyea; Kohl, Paul A.

    2011-10-01

    A solvent processable, low water uptake, partially fluorinated copoly(arylene ether) functionalized with pendant quaternary ammonium groups (QAPAE) was synthesized and uses as the ionomer in alkaline electrodes on fuel cells. The quaternized polymers containing fluorinated biphenyl groups were synthesized via chloromethylation of copoly(arylene ether) followed by amination with trimethylamine. The resulting ionomers were very soluble in polar, aprotic solvents. Highly aminated ionomers had conductivities approaching 10 mS cm-1 at room temperature. Compared to previous ionomers based on quaternized poly(arylene ether sulfone) (QAPSF) with similar ion exchange capacity (IEC), the water uptake of QAPAE was significantly less due to the hydrophobic octafluoro-biphenyl groups in the backbone. The performance of the fuel cell electrodes made with the QAPAE ionomers was evaluated as the cathode on a hybrid AEM/PEM fuel cell. The QAPAE alkaline ionomer electrode with IEC = 1.22 meq g-1 had superior performance to the electrodes prepared with QAPSF, IEC = 1.21 meq g-1 at 25 and 60 °C in a H2/O2 fuel cell. The peak power densities at 60 °C were 315 mW cm-2 for QAPAE electrodes and 215 mW cm-2 for QAPSF electrodes.

  2. Graphene-based battery electrodes having continuous flow paths

    DOEpatents

    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.

  3. Hybrid Air-Electrode for Li/Air Batteries

    SciTech Connect

    Xiao, Jie; Xu, Wu; Wang, Deyu; Zhang, Jiguang

    2010-01-20

    A novel hybrid air-electrode is designed to improve the power density of Li/air batteries operating in an ambient environment. Three lithium insertion materials, MnO2, V2O5, and CFx (x = 1.0 to 1.15), are mixed with activated carbon to prepare different hybrid air-electrodes used in Li/air batteries. When compared with pure carbon-based Li/air batteries, the batteries using hybrid air-electrodes demonstrate significantly improved power capacities, especially for the CFx-based hybrid Li/air batteries. Because it is hydrophobic, CFx also facilitates the formation of air-flow channels in the carbon matrix, and alleviates air-electrode blocking problem during the discharge process. These hybrid air-electrodes provide a promising approach to improve the power density of Li/air batteries.

  4. Battery Electrode Materials with High Cycle Lifetimes

    SciTech Connect

    Prof. Brent Fultz

    2001-06-29

    In an effort to understand the capacity fade of nickel-metal hydride (Ni-MH) batteries, we performed a systematic study of the effects of solute additions on the cycle life of metal hydride electrodes. We also performed a series of measurements on hydrogen absorption capacities of novel carbon and graphite-based materials including graphite nanofibers and single-walled carbon nanotubes. Towards the end of this project we turned our attention to work on Li-ion cells with a focus on anode materials.

  5. Spinel electrodes for rechargeable lithium batteries.

    SciTech Connect

    Thackeray, M. M.

    1999-11-10

    This paper gives a historical account of the development of spinel electrodes for rechargeable lithium batteries. Research in the late 1970's and early 1980's on high-temperature . Li/Fe{sub 3}O{sub 4} cells led to the evaluation of lithium spinels Li[B{sub 2}]X{sub 4} at room temperature (B = metal cation). This work highlighted the importance of the [B{sub 2}]X{sub 4}spinel framework as a host electrode structure and the ability to tailor the cell voltage by selection of different B cations. Examples of lithium-ion cells that operate with spinel anode/spinel cathode couples are provided. Particular attention is paid to spinels within the solid solution system Li{sub 1+x}Mn{sub 2-x}O{sub 4} (0 {le} x {le} 0.33).

  6. Lightweight Fibrous Ni Electrodes For Ni/H2 Batteries

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1991-01-01

    Fibrous nickel plaque electrode material reduces weight of nickel/hydrogen batteries by 40 percent. Discharge voltage and discharge time of fibrous electrode greater than those of equivalent standard sintered-powder electrode. Expected to lead to improvements in performances, increases in energy densities, and decreases in costs of nickel electrodes.

  7. Long life lithium batteries with stabilized electrodes

    DOEpatents

    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.

  8. Advanced Flow Battery Electrodes: Low-cost, High-Performance 50-Year Electrode

    SciTech Connect

    2010-09-01

    GRIDS Project: Primus Power is developing zinc-based, rechargeable liquid flow batteries that could produce substantially more energy at lower cost than conventional batteries. A flow battery is similar to a conventional battery, except instead of storing its energy inside the cell it stores that energy for future use in chemicals that are kept in tanks that sit outside the cell. One of the most costly components in a flow battery is the electrode, where the electrochemical reactions actually occur. Primus Power is investigating and developing mixed-metal materials for their electrodes that could ultimately reduce the lifetime cost of flow batteries because they are more durable and long-lasting than electrodes found in traditional batteries. Using these electrodes, Primus Power’s flow batteries can be grouped together into robust, containerized storage pods for use by utilities, renewable energy developers, businesses, and campuses.

  9. Lithium electronic environments in rechargeable battery electrodes

    NASA Astrophysics Data System (ADS)

    Hightower, Adrian

    This work investigates the electronic environments of lithium in the electrodes of rechargeable batteries. The use of electron energy-loss spectroscopy (EELS) in conjunction with transmission electron microscopy (TEM) is a novel approach, which when coupled with conventional electrochemical experiments, yield a thorough picture of the electrode interior. Relatively few EELS experiments have been preformed on lithium compounds owing to their reactivity. Experimental techniques were established to minimize sample contamination and control electron beam damage to studied compounds. Lithium hydroxide was found to be the most common product of beam damaged lithium alloys. Under an intense electron beam, halogen atoms desorbed by radiolysis in lithium halides. EELS spectra from a number of standard lithium compounds were obtained in order to identify the variety of spectra encountered in lithium rechargeable battery electrodes. Lithium alloys all displayed characteristically broad Li K-edge spectra, consistent with transitions to continuum states. Transitions to bound states were observed in the Li K and oxygen K-edge spectra of lithium oxides. Lithium halides were distinguished by their systematic chemical shift proportional to the anion electronegativity. Good agreement was found with measured lithium halide spectra and electron structure calculations using a self-consistant multiscattering code. The specific electrode environments of LiC6, LiCoO2, and Li-SnO were investigated. Contrary to published XPS predictions, lithium in intercalated graphite was determined to be in more metallic than ionic. We present the first experimental evidence of charge compensation by oxygen ions in deintercalated LiCoO2. Mossbauer studies on cycled Li-SnO reveal severely defective structures on an atomic scale. Metal hydride systems are presented in the appendices of this thesis. The mechanical alloying of immiscible Fe and Mg powders resulted in single-phase bcc alloys of less than 20

  10. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

    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 0electrodes are disclosed, as are electrochemical cells and batteries containing the electrodes.

  11. A simple solvent method for the recovery of LixCoO2 and its applications in alkaline rechargeable batteries

    NASA Astrophysics Data System (ADS)

    Xu, Yanan; Song, Dawei; Li, Li; An, Cuihua; Wang, Yijing; Jiao, LiFang; Yuan, Huatang

    2014-04-01

    A simple solvent method is proposed for the recovery of waste LixCoO2 from lithium-ion batteries, which employs inexpensive DMF to remove the binder of PVDF. This method is convenient to manipulate and low-cost to apply. Electrochemical investigations indicate that recovered LixCoO2 materials with a small amount of S-doping exhibit excellent properties as negative materials for alkaline rechargeable Ni/Co batteries. At the discharge current density of 100 mA g-1, the LixCoO2 + 1% S electrode displays the max discharge capacity of 357 mAh g-1 and outstanding capacity retention rate of 85.5% after 100 cycles. It could overcome not only the sophisticated, energy-intensive shortcomings of conventional recycling methods, but also the high-cost restriction on alkaline rechargeable Ni/Co batteries.

  12. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Xun, Shidi; Battaglia, Vincent S; Zheng, Honghe

    2014-10-07

    A family of carboxylic acid group containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  13. The alkaline zinc electrode as a mixed potential system

    NASA Technical Reports Server (NTRS)

    Fielder, W. L.

    1979-01-01

    Cathodic and anodic processes for the alkaline zinc electrode in 0.01 molar zincate electrolyte (9 molar hydroxide) were investigated. Cyclic voltammograms and current-voltage curves were obtained by supplying pulses through a potentiostat to a zinc rotating disk electrode. The data are interpreted by treating the system as one with a mixed potential; the processes are termed The zincate and corrosion reactions. The relative proportions of the two processes vary with the supplied potential. For the cathodic region, the cathodic corrosion process predominates at higher potentials while both processes occur simultaneously at a lower potential (i.e., 50 mV). For the anodic region, the anodic zincate process predominates at higher potentials while the anodic corrosion process is dominant at lower potential (i.e., 50 mV) if H2 is present.

  14. Evaluation parameters for the alkaline fuel cell oxygen electrode

    NASA Technical Reports Server (NTRS)

    Singer, J.; Srinivasan, V.

    1985-01-01

    Studies were made of Pt- and Au-catalyzed porous electrodes, designed for the cathode of the alkaline H2/O2 fuel cell, employing cyclic voltammetry and the floating half-cell method. The purpose was to obtain parameters from the cyclic voltammograms which could predict performance in the fuel cell. It was found that a satisfactory relationship between these two types of measurement could not be established; however, useful observations were made of relative performance of several types of carbon used as supports for noble metal catalysts and of some Au catalysts. The best half-cell performance with H2/O2 in a 35 percent KOH electrolyte at 80 C was given by unsupported fine particle Au on Teflon; this electrode is used in the Orbiter fuel cell.

  15. Electrodes for H2 and O2 in alkaline media

    NASA Astrophysics Data System (ADS)

    Shinde, Sachin Maruti; Sharon, Madhuri; Sharon, Maheshwar

    2013-06-01

    Pumice plate and carbon felt are tried as electrode for the oxidation for hydrogen and reduction of oxygen in 30% KOH solution. Pumice plate is found to be not suitable for making large area electrode. Carbon felt after depositing conducting carbon by pyrolysis of camphor is found to be hydrophobic. This was used as an electrode for hydrogen oxidation process after depositing platinum (0.2 mg/cm2). This system gives current density of 9.0mA/cm2 and opens circuit potential of 0.423V VsZn/ZnO22-. It is observed that for oxygen reduction process, carbon felt deposited with conducting carbon is sufficient and there is no need to use any electrocatalyst. It is observed that with carbon felt a current density of 89.56mA/cm2 and open circuit potential 1.272 V VsZn/ZnO22- canbe obtained. An over potential of 37mV and 56mV were obtained with carbon felt electrode for hydrogen oxidation process and oxygen reduction process respectively. It is concluded that carbon felt coated with conducting carbon can be used for hydrogen/oxygen alkaline fuel cell.

  16. Intercalation compounds and electrodes for batteries

    DOEpatents

    Chiang, Yet-Ming; Sadoway, Donald R.; Jang, Young-Il; Huang, Biyan

    2004-09-07

    This invention concerns intercalation compounds and in particular lithium intercalation compounds which have improved properties for use in batteries. Compositions of the invention include particulate metal oxide material having particles of multicomponent metal oxide, each including an oxide core of at least first and second metals in a first ratio, and each including a surface coating of metal oxide or hydroxide that does not include the first and second metals in the first ratio formed by segregation of at least one of the first and second metals from the core. The core may preferably comprise Li.sub.x M.sub.y N.sub.z O.sub.2 wherein M and N are metal atom or main group elements, x, y and z are numbers from about 0 to about 1 and y and z are such that a formal charge on M.sub.y N.sub.z portion of the compound is (4-x), and having a charging voltage of at least about 2.5V. The invention may also be characterized as a multicomponent oxide microstructure usable as a lithium intercalation material including a multiphase oxide core and a surface layer of one material, which is a component of the multiphase oxide core, that protects the underlying intercalation material from chemical dissolution or reaction. In a particular preferred example the multicomponent oxide may be an aluminum-doped lithium manganese oxide composition. Such aluminum-doped lithium manganese oxide compositions, having an orthorhombic structure, also form a part of the invention. In addition, the invention includes articles, particularly electrodes, for batteries formed from the compositions of the invention, and batteries including such electrodes. The invention further relates to a composite intercalation material comprising at least two compounds in which at least one compound has an orthorhombic structure Li.sub.x Al.sub.y Mn.sub.1-y O.sub.2, where y is nonzero, or a mixture of orthorhombic and monoclinic Li.sub.x Al.sub.y Mn.sub.1-y O.sub.2.

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

    NASA Technical Reports Server (NTRS)

    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.

  18. An investigation of zinc electrodes relevant to zinc-air batteries

    SciTech Connect

    Choi, H.S.

    1986-12-01

    The particulate electrode (fluidized bed electrode or moving bed electrode) has been studied to evaluate its possible application to energy storage. The first part of this study is concerned with the effect of current fluctuation on the morphology of zinc electrodeposited on the rotating disc electrode from alkaline zincate electrolyte. The effect of the fluctuation on the morphology was examined by scanning electron microscopy. The deposits under the condition of fluctuating current density were smoother than those formed under constant current density. The second part is concerned with the electrodeposition of zinc from alkaline electrolyte with the cell employing a fluidized bed electrode which simulates the recharge process of the secondary battery employing a particulate electrode. Except at high current density, energy consumption per unit production was less than 3 to 4 kWh/kg which is the characteristic value of conventional electrowinning from acidic solution. A laboratory cell with a particulate zinc electrode and an air counter electrode was constructed and discharge characteristics were studied to evaluate the cell. Energy efficiencies during discharge at 5 and 2.5A were about 20 and 30% respectively.

  19. NiCd battery electrodes, C-150

    NASA Technical Reports Server (NTRS)

    Holleck, G.; Turchan, M.; Hopkins, J.

    1972-01-01

    Electrodes for a nongassing negative limited nickel-cadmium cell are discussed. The key element is the development of cadmium electrodes with high hydrogen overvoltage. For this, the following electrode structures were manufactured and their physical and electrochemical characteristics were evaluated: (1) silver-sinter-based Cd electrodes, (2) Teflon-bonded Cd electrodes, (3) electrodeposited Cd sponge, and (4) Cd-sinter structures.

  20. Cross-linked polyvinyl alcohol films as alkaline battery separators

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Manzo, M. A.; Gonzalez-Sanabria, O. D.

    1982-01-01

    Cross-linking methods were investigated to determine their effect on the performance of polyvinyl alcohol (PVA) films as alkaline battery separators. The following types of cross-linked PVA films are discussed: (1) PVA-dialdehyde blends post-treated with an acid or acid periodate solution (two-step method) and (2) PVA-dialdehyde blends cross-linked during film formation (drying) by using a reagent with both aldehyde and acid functionality (one-step method). Laboratory samples of each cross-linked type of film were prepared and evaluated in standard separator screening tests. The pilot-plant batches of films were prepared and compared to measure differences due to the cross-linking method. The pilot-plant materials were then tested in nickel oxide - zinc cells to compare the two methods with respect to performance characteristics and cycle life. Cell test results are compared with those from tests with Celgard.

  1. Cross-linked polyvinyl alcohol films as alkaline battery separators

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.; Manzo, M. A.; Gonzalez-Sanabria, O. D.

    1983-01-01

    Cross-linking methods have been investigated to determine their effect on the performance of polyvinyl alcohol (PVA) films as alkaline battery separators. The following types of cross-linked PVA films are discussed: (1) PVA-dialdehyde blends post-treated with an acid or acid periodate solution (two-step method) and (2) PVA-dialdehyde blends cross-linked during film formation (drying) by using a reagent with both aldehyde and acid functionality (one-step method). Laboratory samples of each cross-linked type of film were prepared and evaluated in standard separator screening tests. Then pilot-plant batches of films were prepared and compared to measure differences due to the cross-linking method. The pilot-plant materials were then tested in nickel oxide-zinc cells to compare the two methods with respect to performance characteristics and cycle life. Cell test results are compared with those from tests with Celgard.

  2. Rechargeability of alkaline Zn-MnO2 batteries: Experimental and mathematical studies

    NASA Astrophysics Data System (ADS)

    Ingale, Nilesh D.

    Batteries based on manganese dioxide (MnO2) cathodes are good candidates for grid-scale electrical energy storage, as MnO2 is low-cost, relatively energy dense, safe, water-compatible, and non-toxic. Alkaline Zn-MnO2 cells, if cycled at reduced depth of discharge (DOD), have been found to achieve substantial cycle life with battery costs projected to be in the range of $100 to 150/kWh (delivered). Commercialization of rechargeable Zn-MnO2 batteries has in the past been hampered due to poor cycle life. In view of this, the work reported here focuses on the long-term rechargeability of prismatic MnO2 cathodes at reduced DOD when exposed to the effects of Zn anodes and with no additives or specialty materials. Over 3000 cycles is shown to be obtainable at 10% DOD with energy efficiency >80%. The causes of capacity fade during long-term cycling are also investigated and appear to be mainly due to the formation of irreversible manganese oxides in the cathode. Analysis of the data indicates that capacity loss is rapid in the first 250 cycles, followed by a regime of stability that can last for thousands of cycles. A model has been developed that captures the behavior of the cells investigated using measured state of charge (SOC) data as input. An approximate economic analysis is also presented to evaluate the economic viability of Zn-MnO2 batteries based on the experiments reported here. The potential of Zn-MnO2 batteries as starting-lighting-ignition (SLI) batteries was also investigated. The impedance contributing parameters at high discharge rates were identified and their effect at high currents was investigated. It was found that prismatic configuration; optimized electrode thickness, electrolyte concentration and electrode size help to achieve high currents for short period of time. In this work, the potential of Zn-MnO 2 batteries for energy as well as power supply has been successfully investigated.

  3. Assemblies of protective anion exchange membrane on air electrode for its efficient operation in aqueous alkaline electrolyte

    NASA Astrophysics Data System (ADS)

    Bertolotti, Bruno; Chikh, Linda; Vancaeyzeele, Cédric; Alfonsi, Séverine; Fichet, Odile

    2015-01-01

    Aqueous alkaline metal-air batteries represent promising energy storage devices when supplied with atmospheric air. However, under this condition, the air electrode shows a very short life time (i.e. 50 h of operation in 5 M LiOH at -10 mA cm-2), mainly due to the precipitation of carbonates inside the electrode porosity. The air electrode can then be protected by an anion exchange membrane on the electrolyte side. In this paper, we demonstrate that the efficiency of this protective membrane depends on the assembly method on the electrode. When a modified poly(epichlorohydrin) (PECH) network is synthesized directly on the electrode, the polymer seeps inside the electrode porosity, and a suitable interface inducing negligible additional polarization in comparison with classical pressure-assembled membranes is obtained. This protected electrode shows improved stability of up to 160 h of operation in 5 M LiOH. This performance is improved to 350 h by adjusting the conductivity and the ionic exchange capacity. Finally, the interest of interpenetrating polymer network (IPN) architecture compared to a single network is confirmed. Indeed, an electrode protected with a PECH/poly(2-hydroxyethyl methacrylate) (PHEMA) IPN is stable for 650 h in 5 M LiOH. In addition, degradation process becomes reversible since the assembly can be regenerated, which is not possible for the bare electrode.

  4. Thermally Regenerative Battery with Intercalatable Electrodes and Selective Heating Means

    NASA Technical Reports Server (NTRS)

    Sharma, Pramod K. (Inventor); Narayanan, Sekharipuram R. (Inventor); Hickey, Gregory S. (Inventor)

    2000-01-01

    The battery contains at least one electrode such as graphite that intercalates a first species from the electrolyte disposed in a first compartment such as bromine to form a thermally decomposable complex during discharge. The other electrode can also be graphite which supplies another species such as lithium to the electrolyte in a second electrode compartment. The thermally decomposable complex is stable at room temperature but decomposes at elevated temperatures such as 50 C. to 150 C. The electrode compartments are separated by a selective ion permeable membrane that is impermeable to the first species. Charging is effected by selectively heating the first electrode.

  5. Hydrogen electrode in lead-hydrogen storage batteries. Influence of macroscopic electrode structure on the electrode's electrochemical activity

    SciTech Connect

    Burmistrov, O.A.; Lyzlov, N.Yu.

    1988-03-01

    Optimum matrix materials and features of a hydrogen gas electrode of lead-hydrogen storage batteries were examined. Carbon materials AG-3, SKT-6A and acetylene black were used as the current-collecting base of the electrode in contact with the sulfuric acid electrolyte. High-pressure polyethylene powder or fluoropolymer were used as wetproofing agents and as electrode binders. Platinum was applied to the electrodes, tested in a gaseous hydrogen saturated cell and linear-scan voltammograms of the electrodes were recorded. Polarization comparable with that found for the lead-dioxide electrode was produced when current was drawn from the hydrogen electrodes.

  6. Bending properties of nickel electrodes for nickel-hydrogen batteries

    NASA Astrophysics Data System (ADS)

    Lerch, Bradley

    1995-04-01

    Recent changes in manufacturing have resulted in nickel-hydrogen batteries which fail prematurely by electrical shorting. This is believed to be a result of a blistering problem in the nickel electrodes. This study investigates the bending properties of nickel electrodes in an attempt to correlate the bending properties with the propensity of the electrode to blister. Nickel electrodes from three different batches of material were tested in both the as-received and impregnated forms. Effects of specimen curvature and position within the electrode on the bending strength were studied and within-electrode and batch-to-batch variation were addressed. Two color imaging techniques were employed which allowed differentiation of phases within the electrodes. These techniques aided in distinguishing the relative amounts of nickel hydroxide surface loading on each electrode, relating surface loading to bend strength. Bend strength was found to increase with the amount of surface loading.

  7. Bending Properties of Nickel Electrodes for Nickel-Hydrogen Batteries

    NASA Technical Reports Server (NTRS)

    Lerch, Brad A.; Wilson, Richard M.; Keller, Dennis; Corner, Ralph

    1995-01-01

    Recent changes in manufacturing have resulted in nickel-hydrogen batteries that fail prematurely by electrical shorting, This failure is believed to be a result of a blistering problem in the nickel electrodes. In this study the bending properties of nickel electrodes are investigated in an attempt to correlate the bending properties of the electrode with its propensity to blister. Nickel electrodes from three different batches of material were tested in both the as-received and impregnated forms. The effects of specimen curvature and position within the electrode on the bending strength were studied, and within-electrode and batch-to-batch variations were addressed. Two color-imaging techniques were employed to differentiate between the phases within the electrodes. These techniques aided in distinguishing the relative amounts of nickel hyroxide surface loading on each electrode, thereby relating surface loading to bend strength. Bend strength was found to increase with the amount of surface loading.

  8. Bending properties of nickel electrodes for nickel-hydrogen batteries

    NASA Technical Reports Server (NTRS)

    Lerch, Bradley

    1995-01-01

    Recent changes in manufacturing have resulted in nickel-hydrogen batteries which fail prematurely by electrical shorting. This is believed to be a result of a blistering problem in the nickel electrodes. This study investigates the bending properties of nickel electrodes in an attempt to correlate the bending properties with the propensity of the electrode to blister. Nickel electrodes from three different batches of material were tested in both the as-received and impregnated forms. Effects of specimen curvature and position within the electrode on the bending strength were studied and within-electrode and batch-to-batch variation were addressed. Two color imaging techniques were employed which allowed differentiation of phases within the electrodes. These techniques aided in distinguishing the relative amounts of nickel hydroxide surface loading on each electrode, relating surface loading to bend strength. Bend strength was found to increase with the amount of surface loading.

  9. NiCd battery electrodes, C-150

    NASA Technical Reports Server (NTRS)

    Holleck, G.

    1971-01-01

    A research program to develop and evaluate electrodes for a nongassing negative limited nickel-cadmium cell is described. The concept of the negative limited cell and its implications on electrode structure are discussed. The key element is the development of a cadmium electrode with high hydrogen overvoltage. For this, Teflon-bonded Cd electrodes and silver-sinter based Gc electrodes were manufactured and in preliminary experiments their physical and electrochemical characteristics were evaluated. Hydrogen evolution on cadmium was found to occur approximately 100 mV more cathodic than on silver. Both electrode structures exhibit a fairly sharp potential rise at the end of the charging cycle and the advent of gas evolution occurs at potentials between -1.2 and -1.3 V versus a Hg/HgO reference electrode. These results are compared with conventional Ni-sinter based Cd electrodes.

  10. Positive electrodes of nickel-cadmium batteries

    NASA Technical Reports Server (NTRS)

    Wabner, D. W.; Kandler, L.; Krienke, W.

    1985-01-01

    Ni hydroxide sintered electrodes which are filled electrochemically are superior to chemically treated electrodes. In the electrochemical process, the hydroxide grows on the Ni grains and possesses a well-defined porous structure. Diffusion and conducting mechanisms are therefore facilitated.

  11. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Battaglia, Vincent S.; Park, Sang -Jae

    2015-10-06

    A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  12. Electronically conductive polymer binder for lithium-ion battery electrode

    SciTech Connect

    Liu, Gao; Xun, Shidi; Battaglia, Vincent S.; Zheng, Honghe; Wu, Mingyan

    2015-07-07

    A family of carboxylic acid groups containing fluorene/fluorenon copolymers is disclosed as binders of silicon particles in the fabrication of negative electrodes for use with lithium ion batteries. Triethyleneoxide side chains provide improved adhesion to materials such as, graphite, silicon, silicon alloy, tin, tin alloy. These binders enable the use of silicon as an electrode material as they significantly improve the cycle-ability of silicon by preventing electrode degradation over time. In particular, these polymers, which become conductive on first charge, bind to the silicon particles of the electrode, are flexible so as to better accommodate the expansion and contraction of the electrode during charge/discharge, and being conductive promote the flow battery current.

  13. Alkali metal ion battery with bimetallic electrode

    SciTech Connect

    Boysen, Dane A; Bradwell, David J; Jiang, Kai; Kim, Hojong; Ortiz, Luis A; Sadoway, Donald R; Tomaszowska, Alina A; Wei, Weifeng; Wang, Kangli

    2015-04-07

    Electrochemical cells having molten electrodes having an alkali metal provide receipt and delivery of power by transporting atoms of the alkali metal between electrode environments of disparate chemical potentials through an electrochemical pathway comprising a salt of the alkali metal. The chemical potential of the alkali metal is decreased when combined with one or more non-alkali metals, thus producing a voltage between an electrode comprising the molten the alkali metal and the electrode comprising the combined alkali/non-alkali metals.

  14. FeS anchored reduced graphene oxide nanosheets as advanced anode material with superior high-rate performance for alkaline secondary batteries

    NASA Astrophysics Data System (ADS)

    Shangguan, Enbo; Guo, Litan; Li, Fei; Wang, Qin; Li, Jing; Li, Quanmin; Chang, Zhaorong; Yuan, Xiao-Zi

    2016-09-01

    A new nanocomposite formulation of the iron-based anode for alkaline secondary batteries is proposed. For the first time, FeS nanoparticles anchored on reduced graphene oxide (RGO) nanosheets are synthesized via a facile, environmentally friendly direct-precipitation approach. In this nanocomposite, FeS nanoparticles are anchored uniformly and tightly on the surface of RGO nanosheets. As an alkaline battery anode, the FeS@RGO electrode delivers a superior high-rate charge/discharge capability and outstanding cycling stability, even at a condition without any conductive additives and a high electrode loading of ∼40 mg cm-2. At high charge/discharge rates of 5C, 10C and 20C (6000 mA g-1), the FeS@RGO electrode presents a specific capacity of ∼288, 258 and 220 mAh g-1, respectively. Moreover, the FeS@RGO electrode exhibits an admirable long cycling stability with a superior capacity retention of 87.6% for 300 cycles at a charge/discharge rate of 2C. The excellent electrochemical properties of the FeS@RGO electrode can be stemmed from the high specific surface area, peculiar electric conductivity and robust sheet-anchored structure of the FeS@RGO nanocomposite. By virtue of its superior fast charge/discharge properties, the FeS@RGO nanocomposite is suitable as an advanced anode material for high-performance alkaline secondary batteries.

  15. Synthesis of cobalt oxide-reduced graphene nanocomposite and its enhanced electrochemical properties as negative material for alkaline secondary battery

    NASA Astrophysics Data System (ADS)

    Xu, Yanan; Wang, Xiaofeng; An, Cuihua; Wang, Yijing; Jiao, Lifang; Yuan, Huatang

    2014-12-01

    A potential negative electrode material Co3O4@rGO is synthesized via a facile reflux condensation route. The electrochemical performances of Co3O4@rGO composite for alkaline rechargeable Ni/Co batteries have been systemically investigated for the first time. The reduced-graphene can remarkably enhance the electrochemical activity of Co3O4 materials, leading to a notable improvement of discharge capacity, cycle stability and rate capability. Interestingly, the maximum discharge capacity of Co3O4@rGO-20 (additive amount of GO is 20 mg) electrode can reach 511.4 mAh g-1 with the capacity retention of 89.1% after 100 cycles at a discharge current of 100 mA g-1. A properly electrochemical reaction mechanism of Co3O4@rGO electrode is also constructed in detail.

  16. Stabilization of insertion electrodes for lithium batteries.

    SciTech Connect

    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.

  17. Advanced inorganic separators for alkaline batteries and method of making the same

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W. (Inventor)

    1983-01-01

    A flexible, porous battery separator includes a coating applied to a porous, flexible substrate. The coating comprises: (1) a thermoplastic rubber-based resin which is insoluble and unreactive in the alkaline electrolyte, (2) a polar organic plasticizer which is reactive with the alkaline electrolyte to produce a reaction product which contains a hydroxyl group and/or a carboxylic acid group, and (3) a mixture of polar particulate filler materials which are unreactive with the electrode. The mixture comprises at least one first filler material having a surface area of greater than 25 sq meters/gram, at last one second filler material having a surface area of 10 to 25 sq meters/gram. The volume of the mixture of filler materials is less than 45% of the total volume of the fillers and the binder. The filler surface area per gram of binder is about 20 to 60 sq meters/gram, and the amount of plasticizer is sufficient to coat each filler particle.

  18. Reinforced Electrode Architecture for a Flexible Battery with Paperlike Characteristics

    SciTech Connect

    Gaikwad, AM; Chu, HN; Qeraj, R; Zamarayeva, AM; Steingart, DA

    2013-02-10

    Compliant energy storage has not kept pace with flexible electronics. Herein we demonstrate a technique to reinforce arbitrary battery electrodes by supporting them with mechanically tough, low-cost fibrous membranes, which also serve as the separator. The membranes were laminated to form a full cell, and this stacked membrane reinforcement bears the loads during flexing. This technique was used to make a high energy density, nontoxic Zn-MnO2 battery with printed current collectors. The Zn and MnO2 electrodes were prepared by using a solution-based embedding process. The cell had a nominal potential of 1.5 V and an effective capacity of approximately 3 mA h cm(-2). We investigated the effect of bending and fatigue on the electrochemical performance and mechanical integrity of the battery. The battery was able to maintain its capacity even after 1000 flex cycles to a bend radius of 2.54 cm. The battery showed an improvement in discharge capacity (ca. 10%) if the MnO2 electrode was flexed to tension as a result of the improvement of particle-to-particle contact. In a demonstration, the flexible battery was used to power a light-emitting diode display integrated with a strain sensor and microcontroller.

  19. Graphene-based integrated electrodes for flexible lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Shi, Ying; Wen, Lei; Zhou, Guangmin; Chen, Jing; Pei, Songfeng; Huang, Kun; Cheng, Hui-Ming; Li, Feng

    2015-06-01

    We have prepared flexible free-standing electrodes with anode and cathode active materials deposited on a highly conductive graphene membrane by a two-step filtration method. Compared with conventional electrodes using metal as current collectors, these electrodes have displayed stronger adhesion, superior electrochemical performance, higher energy density, and better flexibility. A full lithium ion battery assembled by adopting these graphene-based electrodes has showed high rate capability and long cyclic life. We have also assembled a thin, lightweight, and flexible lithium ion battery with poly-(dimethyl siloxane) sheets as packaging material to light a red light-emitting diode. This flexible battery can be easily bent without structural failure or performance loss and operated well under a bent state. The fabrication process of these graphene-based integrated electrodes only has two filtration steps; thus it is easy to scale up. These results suggest great potential for these graphene-based flexible batteries in lightweight, bendable, and wearable electronic devices.

  20. Recovery of pure ZnO nanoparticles from spent Zn-MnO₂ alkaline batteries.

    PubMed

    Deep, Akash; Kumar, Kamal; Kumar, Parveen; Kumar, Pawan; Sharma, Amit L; Gupta, Bina; Bharadwaj, Lalit M

    2011-12-15

    The recovery of pure ZnO (zinc oxide) nanoparticles from spent Zn-Mn dry alkaline batteries is reported. Spent batteries were dismantled to separate the contained valuable metals of the cell electrodes in the form of black powder. Treatment of this black powder with 5 mol L(-1) HCl produced leach liquor, primarily containing 2.90 g L(-1) Zn and 2.02 g L(-1) Mn. Selective and quantitative liquid-liquid extraction of Zn(II) was then carried out in three counter current steps by using Cyanex 923 (0.10 mol L(-1) in n-hexane). Zn(II) distributed in the organic phase as complex ZnCl(2)·2R (R = Cyanex 923 molecule). The metal loaded organic phase was subjected to combust at 600 °C to yield pure ZnO nanoparticles (40-50 nm). Important characteristics of the synthesized nanoparticles were investigated by field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDX), X-ray diffraction spectroscopy (XRD), and atomic force microscopy (AFM). PMID:22050779

  1. Disc electrode and busbar for an electrochemical battery

    SciTech Connect

    Goebel, F.; Batson, D.C.; McHugh, W.T.

    1993-07-13

    An electrochemical battery is described comprising: a case having a cover; a pair of positive and negative polarity terminals extending externally of the battery; a pair of busbar assemblies, one for each of the terminals and connected thereto within the case, each assembly comprising: a pair of inner busbars; and an outer busbar adjacent the inner busbars between the inner busbars and the case; a stack of separate partially open disc electrodes comprising a first plurality of anode elements and a second plurality of cathode elements, the respective anode and cathode elements having electrode tabs welded to the inner and outer busbars of corresponding assemblies; separator means positioned between adjacent pairs of the disc electrodes; and an electrolyte solution surrounding the disc electrodes, separator means and busbars.

  2. Secondary battery containing zinc electrode with modified separator and method

    DOEpatents

    Poa, D.S.

    1984-02-16

    A battery containing a zinc electrode with a porous separator between the anode and cathode. The separator is a microporous substrate carrying therewith an organic solvent of benzene, toluene or xylene with a tertiary organic amine therein, wherein the tertiary amine has three carbon chains each containing from six to eight carbon atoms. The separator reduces the rate of zinc dentrite growth in the separator during battery operation prolonging battery life by preventing short circuits. A method of making the separator is also disclosed.

  3. Secondary battery containing zinc electrode with modified separator and method

    DOEpatents

    Poa, David S.; Yao, Neng-Ping

    1985-01-01

    A battery containing a zinc electrode with a porous separator between the anode and cathode. The separator is a microporous substrate carrying therewith an organic solvent of benzene, toluene or xylene with a tertiary organic amine therein, wherein the tertiary amine has three carbon chains each containing from six to eight carbon atoms. The separator reduces the rate of zinc dentrite growth in the separator during battery operation prolonging battery life by preventing short circuits. A method of making the separator is also disclosed.

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

    NASA Astrophysics Data System (ADS)

    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.

  5. Frequency response measurements in battery electrodes

    NASA Technical Reports Server (NTRS)

    Thomas, Daniel L.

    1992-01-01

    Electrical impedance spectroscopy was used to investigate the behavior of porous zinc, silver, cadmium, and nickel electrodes. State of charge could be correlated with impedance data for all but the nickel electrodes. State of health was correlated with impedance data for two AgZn cells, one apparently good and the other bad. The impedance data was fit to equivalent circuit models.

  6. Bending Properties of Nickel Electrodes for Nickel-Hydrogen Batteries

    NASA Technical Reports Server (NTRS)

    Lerch, Brad A.; Wilson, Richard M.; Keller, Dennis; Corner, Ralph

    1996-01-01

    Recent changes in manufacturing have resulted in nickel-hydrogen batteries that fail prematurely by electrical shorting. This failure is believed to be a result of a blistering problem in the nickel electrodes. In this study, the bending properties of nickel electrodes are investigated in an attempt to correlate the bending properties of the electrode with its propensity to blister. Nickel electrodes from three different batches of material were tested in both the as-received and impregnated forms. The effects of specimen curvature and position within the electrode on the bending strength were studied, and within-electrode and batch-to-batch variations were addressed. Bend strength was found to increase with the amount of surface loading.

  7. High performance positive electrode for a lead-acid battery

    NASA Technical Reports Server (NTRS)

    Kao, Wen-Hong (Inventor); Bullock, Norma K. (Inventor); Petersen, Ralph A. (Inventor)

    1994-01-01

    An electrode suitable for use as a lead-acid battery plate is formed of a paste composition which enhances the performance of the plate. The paste composition includes a basic lead sulfate, a persulfate and water. The paste may also include lead oxide and fibers. An electrode according to the invention is characterized by good strength in combination with high power density, porosity and surface area.

  8. Non-gassing nickel-cadmium battery electrodes and cells

    NASA Technical Reports Server (NTRS)

    Luksha, E.; Gordy, D. J.

    1972-01-01

    The concept of a negative limited nongassing nickel-cadmium battery was demonstrated by constructing and testing practical size experimental cells of approximately 25 Ah capacity. These batteries operated in a gas-free manner and had measured energy densities of 10-11 Wh/lb. Thirty cells were constructed for extensive testing. Some small cells were tested for over 200 cycles at 100% depth. For example, a small cell with an electrodeposited cadmium active mass on a silver screen still had 55% of its theoretical capacity (initial efficiency was 85%). There was no evidence of deterioration of gassing properties with cycling of the nickel electrodes. The charge temperature was observed to be the most critical variable governing nickel electrode gassing. This variable was shown to be age dependent. Four types of cadmium electrodes were tested: an electrodeposited cadmium active mass on a cadmium or silver substrate, a porous sintered silver substrate based electrode, and a Teflon bonded pressed cadmium electrode. The electrodeposited cadmium mass on a silver screen was found to be the best all-around electrode from a performance point of view and from the point of view of manufacturing them in a size required for a 25 Ah size battery.

  9. Alkaline composite PEO-PVA-glass-fibre-mat polymer electrolyte for Zn-air battery

    NASA Astrophysics Data System (ADS)

    Yang, Chun-Chen; Lin, Sheng-Jen

    An alkaline composite PEO-PVA-glass-fibre-mat polymer electrolyte with high ionic conductivity (10 -2 S cm -1) at room temperature has been prepared and applied to solid-state primary Zn-air batteries. The electrolyte shows excellent mechanical strength. The electrochemical characteristics of the batteries were experimentally investigated by means of ac impedance spectroscopy and galvanostatic discharge. The results indicate that the PEO-PVA-glass-fibre-mat composite polymer electrolyte is a promising candidate for application in alkaline primary Zn-air batteries.

  10. Predoped conductive polymers as battery electrode materials

    SciTech Connect

    Jow, T.R.; Shacklette, L.W.

    1989-02-14

    An improved battery is described. The anode consists of one or more conjugated backbone polymers and one or more electroactive materials selected from the group consisting of metals which alloy with alkali metals and alkali metal cation inserting material. The electrolyte consists of an organic solvent and an alkali-metal salt. There is also a cathode alkali-metal cations from the electrolyte being inserted into the anode as a metal alloy or as an inserted ion in the alkali metal cation inserting material during the charging of the battery; the improvement comprises an anode in which the conjugated backbone polymers contained in the anode have been predoped with one or more alkali metal cations to the reduced state prior to incorporation of the anode into the battery.

  11. Workshop on electrodes for flowing solution batteries

    NASA Astrophysics Data System (ADS)

    Nanis, L.

    1981-02-01

    The electrochemical technology of aqueous secondary cells with flowing electrolyte solutions was addressed. Emphasis was placed on the significant parameters believed to govern the performance of the two basic types of electrodes now in use: a porous flow through electrode (PFTE), and an impervious flow by electrode. Progress, problems, and prospects were informally discussed. Key topics included: (current distribution in FTPE; conversion efficiency, segmented FTPE studies; general discussion on FTPE parameters; surface activation; application of FTPE to waste recovery; Exxon zinc bromine flow by system, FTPE in NASA redox energy storage; and application of FTPE in Lockheed zinc ferricyanide redox system). In generally comparing flow through to flow by electrodes, there were some surprising differences arising from experimental results that did not fit conventional thinking.

  12. Direct Solar Charging of an Organic-Inorganic, Stable, and Aqueous Alkaline Redox Flow Battery with a Hematite Photoanode.

    PubMed

    Wedege, Kristina; Azevedo, João; Khataee, Amirreza; Bentien, Anders; Mendes, Adélio

    2016-06-13

    The intermittent nature of the sunlight and its increasing contribution to electricity generation is fostering the energy storage research. Direct solar charging of an auspicious type of redox flow battery could make solar energy directly and efficiently dispatchable. The first solar aqueous alkaline redox flow battery using low cost and environmentally safe materials is demonstrated. The electrolytes consist of the redox couples ferrocyanide and anthraquinone-2,7-disulphonate in sodium hydroxide solution, yielding a standard cell potential of 0.74 V. Photovoltage enhancement strategies are demonstrated for the ferrocyanide-hematite junction by employing an annealing treatment and growing a layer of a conductive polyaniline polymer on the electrode surface, which decreases electron-hole recombination. PMID:27151516

  13. Lightweight fibrous nickel electrodes for nickel-hydrogen batteries

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1989-01-01

    The NASA Lewis Research Center is currently developing nickel electrodes for nickel-hydrogen batteries. These electrodes are lighter in weight and have higher energy densities than the heavier state-of-the-art sintered nickel electrodes. Lightweight fibrous materials or plaques are used as conductive supports for the nickel hydroxide active material. These materials are commercial products that are fabricated into nickel electrodes by electrochemically impregnating them with active material. Evaluation is performed in half cells structured in the bipolar configuration. Initial performance tests include capacity measurements at five discharge levels, C/2, 1.0C, 1.37C, 2.0C, and 2.74C. The electrodes that pass the initial tests are life cycle-tested in a low Earth orbit regime at 80 percent depth of discharge.

  14. Hierarchically porous graphene as a lithium-air battery electrode.

    PubMed

    Xiao, Jie; Mei, Donghai; Li, Xiaolin; Xu, Wu; Wang, Deyu; Graff, Gordon L; Bennett, Wendy D; Nie, Zimin; Saraf, Laxmikant V; Aksay, Ilhan A; Liu, Jun; Zhang, Ji-Guang

    2011-11-01

    The lithium-air battery is one of the most promising technologies among various electrochemical energy storage systems. We demonstrate that a novel air electrode consisting of an unusual hierarchical arrangement of functionalized graphene sheets (with no catalyst) delivers an exceptionally high capacity of 15000 mAh/g in lithium-O(2) batteries which is the highest value ever reported in this field. This excellent performance is attributed to the unique bimodal porous structure of the electrode which consists of microporous channels facilitating rapid O(2) diffusion while the highly connected nanoscale pores provide a high density of reactive sites for Li-O(2) reactions. Further, we show that the defects and functional groups on graphene favor the formation of isolated nanosized Li(2)O(2) particles and help prevent air blocking in the air electrode. The hierarchically ordered porous structure in bulk graphene enables its practical applications by promoting accessibility to most graphene sheets in this structure. PMID:21985448

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

    DOEpatents

    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.

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

    DOEpatents

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

    2014-10-28

    Method of forming lithium-containing electrolytes are provided using wet chemical synthesis. In some examples, the lithium containing electrolytes 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 of .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. Layered electrodes for lithium cells and batteries

    DOEpatents

    Johnson; Christopher S. , Thackeray; Michael M. , Vaughey; John T. , Kahaian; Arthur J. , Kim; Jeom-Soo

    2008-04-15

    Lithium metal oxide compounds of nominal formula Li.sub.2MO.sub.2, in which M represents two or more positively charged metal ions, selected predominantly and preferably from the first row of transition metals are disclosed herein. The Li.sub.2MO.sub.2 compounds have a layered-type structure, which can be used as positive electrodes for lithium electrochemical cells, or as a precursor for the in-situ electrochemical fabrication of LiMO.sub.2 electrodes. The Li.sub.2MO.sub.2 compounds of the invention may have additional functions in lithium cells, for example, as end-of-discharge indicators, or as negative electrodes for lithium cells.

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

    NASA Technical Reports Server (NTRS)

    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.

  19. Battery using a metal particle bed electrode

    SciTech Connect

    Evans, James V.; Savaskan, Gultekin

    1991-01-01

    A zinc-air battery in a case including a zinc particle bed supported adjacent the current feeder and diaphragm on a porous support plate which holds the particles but passes electrolyte solution. Electrolyte is recycled through a conduit between the support plate and top of the bed by convective forces created by a density of differential caused by a higher concentration of high density discharge products in the interstices of the bed than in the electrolyte recycle conduit.

  20. Battery using a metal particle bed electrode

    SciTech Connect

    Evans, J.V.; Savaskan, G.

    1991-04-09

    A zinc-air battery in a case is described including a zinc particle bed supported adjacent the current feeder and diaphragm on a porous support plate which holds the particles but passes electrolyte solution. Electrolyte is recycled through a conduit between the support plate and top of the bed by convective forces created by a density of differential caused by a higher concentration of high density discharge products in the interstices of the bed than in the electrolyte recycle conduit. 7 figures.

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

    PubMed

    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. PMID:26765041

  2. Lightweight nickel electrode for nickel hydrogen cells and batteries

    NASA Technical Reports Server (NTRS)

    Britton, D. L.

    1986-01-01

    The nickel electrode was identified as the heaviest component of the nickel hydrogen (NiH2) battery. The NASA Lewis Research Center is developing nickel electrodes for NiH2 battery devices which will be lighter in weight and have higher energy densities when cycled under a low Earth orbit regime at deep depths of discharge. Lightweight plaques are first exposed to 31 percent potassium hydroxide for 3 months to determine their suitability for use as electrode substrates from a chemical corrosion standpoint. Pore size distribution and porosity of the plaques are then measured. The lightweight plaques examined are nickel foam, nickel felt, nickel plastic and nickel plated graphite. Plaques are then electrochemically impregnated in an aqueous solution. Initial characterization tests of the impregnated plaques are performed at five discharge levels, C/2, 1.0 C, 1.37 C, 2.0C, and 2.74 C rates. Electrodes that passed the initial characterization screening test will be life cycle tested. Lightweight electrodes are approximately 30 to 50 percent lighter in weight than the sintered nickel electrode.

  3. Lightweight nickel electrode for nickel hydrogen cells and batteries

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1986-01-01

    The nickel electrode was identified as the heaviest component of the nickel hydrogen (NiH2) battery. The NASA Lewis Research Center is developing nickel electrodes for NiH2 battery devices which will be lighter in weight and have higher energy densities when cycled under a low Earth orbit regime at deep depths of discharge. Lightweight plaques are first exposed to 31 percent potassium hydroxide for 3 months to determine their suitability for use as electrode substrates from a chemical corrosion standpoint. Pore size distribution and porosity of the plaques are then measured. The lightweight plaques examined are nickel foam, nickel felt, nickel plastic and nickel plated graphite. Plaques are then electrochemically impregnated in an aqueous solution. Initial characterization tests of the impregnated plaques are performed at five discharge levels, C/2, 1.0 C, 1.37 C, 2.0 C, and 2.74 C rates. Electrodes that passed the initial characterization screening test will be life cycle tested. Lightweight electrodes are approximately 30 to 50 percent lighter in weight than the sintered nickel electrode.

  4. Towards uniformly dispersed battery electrode composite materials: Characteristics and performance

    DOE PAGESBeta

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

    2016-01-14

    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 formore » 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. In conclusion, the study illustrates the importance of considering electronic conductivity, electron transfer, and ion transport in the design of environments incorporating active nanomaterials.« less

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

    SciTech Connect

    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.

  6. Porosity measurements of electrodes used in lead-acid batteries

    NASA Astrophysics Data System (ADS)

    Ferg, E. E.; Loyson, P.; Rust, N.

    A method is presented that determines the porosity of a complete electrode plate used in lead-acid batteries. It requires only elementary equipment and is simple to operate, so that laboratory workers can use it as a routine method during manufacturing to determine the complete electrode's average porosity over a range of electrode sizes and types of both flat plate and tubular configuration. The method makes use of Archimedes' principle and uses glycerol as displacement medium. This allows for the porosity determination of both cured and formed positive and negative electrodes, without the detrimental effect of lead oxidation, which is common when using water as a displacement medium. The study showed that the method of using glycerol as a displacement medium gave on average, good repeatable results for both cured and formed positive and negative electrode plates used in the manufacture of automotive lead-acid batteries. The porosity results of the method were compared to the results obtained using Hg porosimetry, where a statistical paired t-test showed the two techniques to produce comparable results for all types of plates analyzed. The porosity of various plates was compared to the surface area of the respective active material of both positive and negative electrodes. These results showed unusual trends in that, depending on the manufacturing conditions, the surface area of formed positive electrodes could vary significantly from sample to sample of different batches without little change in its respective porosity. The surface area of different formed negative electrodes, however, would only vary slightly with significant changes in their corresponding porosity. The glycerol displacement method was also shown to be suitable to determine the effective porosity of cured and formed positive tubular electrodes.

  7. Effect of various alkaline metal ions on electrochemical behavior of lead electrode in sulfuric acid solution

    NASA Astrophysics Data System (ADS)

    Hirai, Nobumitsu; Yamamoto, Yui

    2015-10-01

    The effect of various alkaline metal ions on electrochemical behavior of lead electrode in sulfuric acid solution has been investigated. It was found that "the specific anodic oxidation peak" appears at the cathodic scan in cyclic voltammogram of lead electrode in sulfuric acid solution containing Li2SO4, K2SO4, Na2SO4, Rb2SO4, or Cs2SO4. The height of the specific anodic oxidation peak varies with the alkaline sulfate in the solution; K2SO4 >> Na2SO4 > Cs2SO4 > Rb2SO4 > Li2SO4. It should be note that alkaline ions exist in lead sulfate formed on lead electrode in sulfuric acid solution containing potassium sulfate when the electrode was immersed in the solution at the rest potential for more than 1 h.

  8. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2006-11-14

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0batteries are disclosed with anode, cathode and electrolyte as are batteries of several cells connected in parallel or series or both.

  9. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2004-01-13

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0batteries are disclosed with anode, cathode and electrolyte as are batteries of several cells connected in parallel or series or both.

  10. Environmental technology verification report: Rechargeable alkaline household battery system, Rayovac Corporation Renewal[trademark

    SciTech Connect

    Escarda, T.; Lewis, N.

    1999-03-01

    The EPA's ETV Program, in partnership with recognized testing organizations, objectively and systematically documents the performance of commercial ready technologies. Together, with the full participation of the technology developer, they develop plans, conduct tests, collect and analyze data, and report findings. Rayovac redesigned their alkaline household batteries so that they could be recharged. The additional charge cycles extend battery life by increasing the energy capacity, which benefits the environment by generating less waste. The design changes include increased void space, and addition of lead and silver. The Rayovac Renewal[trademark] Rechargeable Alkaline Battery System consists of rechargable alkaline zinc-manganese dioxide 1.5 volt batteries, in sizes AAA, AA, C, and D, and a recharging device for the batteries. Typical consumer applications of household batteries include toys and games, portable audio equipment, cameras, sporting goods equipment, test equipment, personal care products, hearing aids, portable data terminals, sub-notebook computers and personal digital assistants, watches, flashlights, lanterns, and cellular phones. Such applications typically require continuous currents of up to 400 milliamperes (mA), which is within the range of the Renewal[trademark] batteries, sized AA, C, and D. Size AAA can supply up to 150 mA continuous current, which is sufficient for applications such as clocks.

  11. Environmental technology verification report: Rechargeable alkaline household battery system, Rayovac Corporation Renewal{trademark}

    SciTech Connect

    Escarda, T.; Lewis, N.

    1999-03-01

    The EPA`s ETV Program, in partnership with recognized testing organizations, objectively and systematically documents the performance of commercial ready technologies. Together, with the full participation of the technology developer, they develop plans, conduct tests, collect and analyze data, and report findings. Rayovac redesigned their alkaline household batteries so that they could be recharged. The additional charge cycles extend battery life by increasing the energy capacity, which benefits the environment by generating less waste. The design changes include increased void space, and addition of lead and silver. The Rayovac Renewal{trademark} Rechargeable Alkaline Battery System consists of rechargable alkaline zinc-manganese dioxide 1.5 volt batteries, in sizes AAA, AA, C, and D, and a recharging device for the batteries. Typical consumer applications of household batteries include toys and games, portable audio equipment, cameras, sporting goods equipment, test equipment, personal care products, hearing aids, portable data terminals, sub-notebook computers and personal digital assistants, watches, flashlights, lanterns, and cellular phones. Such applications typically require continuous currents of up to 400 milliamperes (mA), which is within the range of the Renewal{trademark} batteries, sized AA, C, and D. Size AAA can supply up to 150 mA continuous current, which is sufficient for applications such as clocks.

  12. Silver-Copper Nanoalloy Catalyst Layer for Bifunctional Air Electrodes in Alkaline Media.

    PubMed

    Wu, Xiaoqiang; Chen, Fuyi; Jin, Yachao; Zhang, Nan; Johnston, Roy L

    2015-08-19

    A carbon-free and binder-free catalyst layer composed of a Ag-Cu nanoalloy on Ni foam was used as the air cathode in a zinc-air battery for the first time. The Ag-Cu catalyst was prepared using pulsed laser deposition. The structures of the catalysts were found to consist of crystalline Ag-Cu nanoalloy particles with an average size of 2.58 nm embedded in amorphous Cu films. As observed in the X-ray photoelectron spectra, the Ag 3d core levels shifted to higher binding energies, whereas the Cu 2p core levels shifted to lower binding energies, indicating alloying of the silver and copper. Rotating disk electrode measurements indicated that the oxygen reduction reaction (ORR) proceeded through a four-electron pathway on the Ag50Cu50 and Ag90Cu10 nanoalloy catalysts in alkaline solution. Moreover, the catalytic activity of Ag50Cu50 in the ORR is more efficient than that of Ag90Cu10. By performing charge and discharge cycling measurements, the Ag50Cu50 catalyst layer was confirmed to have a maximum power density of approximately 86.3 mW cm(-2) and an acceptable cell voltage at 0.863 V for current densities up to 100 mA cm(-2) in primary zinc-air batteries. In addition, a round-trip efficiency of approximately 50% at a current density of 20 mA cm(-2) was also obtained in the test. PMID:26200807

  13. High-performance battery electrodes via magnetic templating

    NASA Astrophysics Data System (ADS)

    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 <4 mAh cm‑2 in conventional electrodes) at practical charge–discharge rates. We demonstrate these capabilities in laboratory cells under various test conditions, including an electric vehicle model drive cycle.

  14. Multi-component intermetallic electrodes for lithium batteries

    DOEpatents

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. Self-Assembled Monolayers of n-Alkanethiols Suppress Hydrogen Evolution and Increase the Efficiency of Rechargeable Iron Battery Electrodes

    SciTech Connect

    Malkhandi, S; Yang, B; Manohar, AK; Prakash, GKS; Narayanan, SR

    2013-01-09

    Iron-based rechargeable batteries, because of their low cost, eco-friendliness, and durability, are extremely attractive for large-scale energy storage. A principal challenge in the deployment of these batteries is their relatively low electrical efficiency. The low efficiency is due to parasitic hydrogen evolution that occurs on the iron electrode during charging and idle stand. In this study, we demonstrate for the first time that linear alkanethiols are very effective in suppressing hydrogen evolution on alkaline iron battery electrodes. The alkanethiols form self-assembled monolayers on the iron electrodes. The degree of suppression of hydrogen evolution by the alkanethiols was found to be greater than 90%, and the effectiveness of the alkanethiol increased with the chain length. Through steady-state potentiostatic polarization studies and impedance measurements on high-purity iron disk electrodes, we show that the self-assembly of alkanethiols suppressed the parasitic reaction by reducing the interfacial area available for the electrochemical reaction. We have modeled the effect of chain length of the alkanethiol on the surface coverage, charge-transfer resistance, and double-layer capacitance of the interface using a simple model that also yields a value for the interchain interaction energy. We have verified the improvement in charging efficiency resulting from the use of the alkanethiols in practical rechargeable iron battery electrodes. The results of battery tests indicate that alkanethiols yield among the highest faradaic efficiencies reported for the rechargeable iron electrodes, enabling the prospect of a large-scale energy storage solution based on low-cost iron-based rechargeable batteries.

  17. Probing the electrochemical properties of biopolymer modified EMD nanoflakes through electrodeposition for high performance alkaline batteries.

    PubMed

    Biswal, Avijit; Minakshi, Manickam; Tripathy, Bankim Chandra

    2016-04-01

    In the present work, a novel biopolymer approach has been made to electrodeposit manganese dioxide from manganese sulphate in a sulphuric acid bath containing chitosan in the absence and presence of glutaraldehyde as a cross-linking agent. Galvanostatically synthesised electrolytic manganese dioxide (EMD) nanoflakes were used as electrode materials and their electrochemical properties with the influence of biopolymer chitosan were systematically characterized. The structural determination, surface morphology and porosity of nanostructured EMD were evaluated using X-ray diffraction, Fourier transform infrared spectroscopy, field emission scanning electron microscopy and nitrogen adsorption-desorption techniques. The results obtained were compared with that of blank EMD (polymer free). The results indicated that the EMD having chitosan cross-linked with glutaraldehyde possesses a reduced particle size and more porous structure than the blank and EMDs synthesized in the presence of chitosan but without glutaraldehyde. The results revealed that chitosan was unable to play any significant role on its own but chitosan in the presence of glutaraldehyde forms a cross-linking structure, which in turn influences the nucleation and growth of the EMDs during electrodeposition. EMDs obtained in the presence of chitosan (1 g dm(-3)) and glutaraldehyde (1% glutaraldehyde) exhibited a reversible and better discharge capacity upon cycling than the blank which showed its typical capacity fading behaviour with cycling. In addition, EMD synthesized in the presence of 1 g dm(-3) chitosan and 2% glutaraldehyde exhibited a superior electrochemical performance than the blank and lower amounts (1%; 1.5%) of glutaraldehyde, showing a stable discharge capacity of 60 mA h g(-1) recorded up to 40 cycles in alkaline KOH electrolyte for a Zn-MnO2 system. Our results demonstrate the potential of using polymer modified EMDs as a new generation of alkaline battery materials. The XPS data show that

  18. Aluminum-ferricyanide battery

    SciTech Connect

    Marsh, C.; Licht, S.L.

    1993-11-29

    A battery capable of producing high current densities with high charge capacity is described which includes an aluminum anode, a ferricyanide electrolyte and a second electrode capable of reducing ferricyanide electrolyte which is either dissolved in an alkaline solution or alkaline seawater solution. The performance of the battery is enhanced by high temperature and high electrolyte flow rates.

  19. Sandwich electrode designed for high performance lithium-ion battery.

    PubMed

    Zhao, Chunsong; Luo, Xi; Chen, Chengmeng; Wu, Hui

    2016-05-01

    We fabricated a sandwich structure Li-ion battery electrode by trapping micron-sized silicon between a copper current collector and a graphene coating. During dynamic electrochemical cycles, the volume change of the silicon can be buffered by the coating through the deformation of soft graphenes. This structure can effectively prevent the silicon particles from escaping from the current collector while keeping the buffered graphene coating integrated and unbroken during deformation. The electrodes could be maintained for 400 cycles at a constant charge capacity of 1000 mA h g(-1). PMID:27117447

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

    NASA Astrophysics Data System (ADS)

    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.

  1. Test Procedures for Characterizing, Evaluating, and Managing Separator Materials used in Secondary Alkaline Batteries

    NASA Technical Reports Server (NTRS)

    Guasp, Edwin; Manzo, Michelle A.

    1997-01-01

    Secondary alkaline batteries, such as nickel-cadmium and silver-zinc, are commonly used for aerospace applications. The uniform evaluation and comparison of separator properties for these systems is dependent upon the measurement techniques. This manual presents a series of standard test procedures that can be used to evaluate, compare, and select separator materials for use in alkaline batteries. Detailed test procedures evaluating the following characteristics are included in this manual: physical measurements of thickness and area weight, dimensional stability measurements, electrolyte retention, resistivity, permeability as measured via bubble pressure, surface evaluation via SEM, chemical stability, and tensile strength.

  2. Composite electrode for storage batteries and the like

    SciTech Connect

    Faber, P.

    1980-09-16

    A metal/synthetic-resin composite electrode for a storage battery or the like is comprised of a perforate metal support which is flanked on both sides by openworks of polyolefin, e.g., partially fluorinated polyolefin, which are welded together within the openings of the support and carry the active material. The polyolefin openworks, together with the active material, are covered in turn with polyester fabric or polyester felt permeable fine porous cover layers.

  3. Modelling of nickel-cadmium batteries using porous electrode theory

    NASA Technical Reports Server (NTRS)

    Timmerman, Paul J.; Di Stefano, Salvador; Glueck, Peter R.; Perrone, David E.

    1991-01-01

    A porous electrode modeling technique is discussed which is considered a viable means for quantitatively predicting Ni-Cd cell performance. The authors describe the integration of the cell model into a battery model useful in the design and operation of aerospace applications. Test data from a sealed boilerplate cell are presented for constant current charge and discharge conditions. Performance predictions for similar cases have been performed, and a comparison to the boilerplate data is made. Areas for further development are also noted.

  4. Microfibrous nickel substrates and electrodes for battery system applications

    NASA Astrophysics Data System (ADS)

    Zhu, Wenhua H.; Durben, Peter J.; Tatarchuk, Bruce J.

    The use of microfibrous nickel substrates is advantageous for increasing the surface area available for the deposition of active material and reducing the substrate weight and consequently, yields a higher specific capacity for nickel hydroxide electrodes. Porous, microfiber-based nickel substrates were produced by sintering a composite preform. The preforms, consisting of nickel fibers with diameters as small as 2 μm and cellulose fibers, were formed using a papermaking process. The fabricated nickel electrodes that included a supporting nickel mesh in the substrate tested in a 26% KOH half-cell delivered a specific capacity of more than 250 mAh/g of the electrode weight (i.e. fibrous substrate, nickel mesh, and active material) at a 1.0 C discharge rate. An Auburn electrode without a nickel mesh tested in the same half-cell attained a higher specific capacity of 268 mAh/g at a 1.37 C discharge rate. The substrates used in these electrodes had porosities of 95-97%, and greatly improved the specific capacity of the nickel electrode. With the use of the microfibrous electrode, improved specific energies of nickel-based cell and battery designs are possible. When assembled in a nickel-hydrogen (Ni-H 2) boilerplate cell, the specific capacity of nearly 230 mAh/g was observed for the nickel electrode at a 0.5 C rate during the 127th cycle test. The results of high specific capacity and quick rise in utilization of microfibrous nickel hydroxide electrodes make these electrodes good candidates for significantly improving the energy density and performance of nickel-hydrogen cells.

  5. Internally folded expanded metal electrode for battery construction

    NASA Technical Reports Server (NTRS)

    Korinek, Paul D. (Inventor); Morgan, Maurice C. (Inventor); Pierce, Doug C. (Inventor)

    1993-01-01

    A battery system is disclosed which includes folded grids of expanded metal inserted through non-conductive substrates and pasted with electrochemically active materials. In the most preferred embodiment, a frame is provided with a plastic insert, and slots are provided in the latter to receive the expanded metal grid. After suitable coinage of the grid and insertion through the plastic film, the grid is sealed and pasted on opposite sides with positive and negative active material. A battery is assembled using one or a plurality of the resulting electrode elements, with separators, to produce a high-power, lead-acid battery. The folded grid provides many of the design benefits of standard bipolar construction.

  6. Sandwich electrode designed for high performance lithium-ion battery

    NASA Astrophysics Data System (ADS)

    Zhao, Chunsong; Luo, Xi; Chen, Chengmeng; Wu, Hui

    2016-05-01

    We fabricated a sandwich structure Li-ion battery electrode by trapping micron-sized silicon between a copper current collector and a graphene coating. During dynamic electrochemical cycles, the volume change of the silicon can be buffered by the coating through the deformation of soft graphenes. This structure can effectively prevent the silicon particles from escaping from the current collector while keeping the buffered graphene coating integrated and unbroken during deformation. The electrodes could be maintained for 400 cycles at a constant charge capacity of 1000 mA h g-1.We fabricated a sandwich structure Li-ion battery electrode by trapping micron-sized silicon between a copper current collector and a graphene coating. During dynamic electrochemical cycles, the volume change of the silicon can be buffered by the coating through the deformation of soft graphenes. This structure can effectively prevent the silicon particles from escaping from the current collector while keeping the buffered graphene coating integrated and unbroken during deformation. The electrodes could be maintained for 400 cycles at a constant charge capacity of 1000 mA h g-1. Electronic supplementary information (ESI) available. See DOI: 10.1039/c5nr09049k

  7. Calcium-Antimony Alloys as Electrodes for Liquid Metal Batteries

    SciTech Connect

    Ouchi, T; Kim, H; Ning, XH; Sadoway, DR

    2014-08-08

    The performance of a calcium-antimony (Ca-Sb) alloy serving as the positive electrode in a Ca vertical bar vertical bar Sb liquid metal battery was investigated in an electrochemical cell, Ca(in Bi) vertical bar LiCl-NaCl-CaCl2 vertical bar Ca(in Sb). The equilibrium potential of the Ca-Sb electrode was found to lie on the interval, 1.2-0.95 V versus Ca, in good agreement with electromotive force (emf) measurements in the literature. During both alloying and dealloying of Ca at the Sb electrode, the charge transfer and mass transport at the interface are facile enough that the electrode potential varies linearly from 0.95 to 0.75 V vs Ca(s) as current density varies from 50 to 500 mA cm(-2). The discharge capacity of the Ca vertical bar vertical bar Sb cells increases as the operating temperature increases due to the higher solubility and diffusivity of Ca in Sb. The cell was successfully cycled with high coulombic efficiency (similar to 100%) and small fade rate (<0.01% cycle(-1)). These data combined with the favorable costs of these metals and salts make the Ca vertical bar vertical bar Sb liquid metal battery attractive for grid-scale energy storage. (C) The Author(s) 2014. Published by ECS. All rights reserved.

  8. Development of anion-conducting ionomer binder solutions for electrodes of solid alkaline fuel cells.

    PubMed

    Shin, Mun-Sik; Kang, Moon-Sung; Park, Jin-Soo

    2014-10-01

    For solid alkaline fuel cell applications, membrane-electrode assemblies (MEAs) should be prepared. Thus, in this study, anion-conducting ionomer binder was prepared for electrodes of MEAs. Specifically, we synthesized water soluble anionic binder solutions based on quaternized chitosan derivatives (QCDs) and cross-linked QCDs and prepared a novel electrode. The electrochemical and physicochemical properties of ionomer binder and electrode were investigated by FT-IR, NMR and ionic conductivity. The ionic conductivity of these cross-linked QCDs was 9.7 x 10(-3) S cm(-1) in deionized water at room temperature. The membrane electrode assemblies (MEAs) were prepared by a spray method and were investigated in terms of cyclic voltammetry, impedance and fuel cell performance. The MEA with the 35 wt% QCD ionomer showed the highest performance and confirmed the successful formation of ionomer binder at the electrode of the MEA by the on-site crosslinking reaction. PMID:25942868

  9. Electrochemical oxidation of hydrazine and its derivatives on the surface of metal electrodes in alkaline media

    NASA Astrophysics Data System (ADS)

    Asazawa, Koichiro; Yamada, Koji; Tanaka, Hirohisa; Taniguchi, Masatoshi; Oguro, Keisuke

    Electrochemical oxidation of hydrazine and its derivatives on the surface of various metal electrodes in alkaline media was investigated. A comparison of various polycrystalline metal electrodes (Ni, Co, Fe, Cu, Ag, Au, and Pt) showed that Co and Ni electrodes have a lower onset potential for hydrazine oxidation than the Pt electrode. The onset oxidation potential of APA (aminopolyacrylamide), a hydrazine derivative (-0.127 V vs. reversible hydrogen electrode, RHE), was similar to that of hydrazine hydrate (-0.178 V vs. RHE) in the case of the Co electrode. APA oxidation was possible because of hydrazine desorption that was caused by APA hydrolysis. The hydrolysis reaction was brought about by a heat treatment. This result suggests that the hydrazine hydrolysis reaction of hydrazine derivatives makes it possible to store hydrazine hydrate safely.

  10. Ultrafine polybenzimidazole (PBI) fibers. [separators for alkaline batteries and dfuel cells

    NASA Technical Reports Server (NTRS)

    Chenevey, E. C.

    1979-01-01

    Mats were made from ultrafine polybenzimidazole (PBI) fibers to provide an alternate to the use of asbestos as separators in fuel cells and alkaline batteries. To minimize distortion during mat drying, a process to provide a dry fibrid was developed. Two fibrid types were developed: one coarse, making mats for battery separators; the other fine, making low permeability matrices for fuel cells. Eventually, it was demonstrated that suitable mat fabrication techniques yielded fuel cell separators from the coarser alkaline battery fibrids. The stability of PBI mats to 45% KOH at 123 C can be increased by heat treatment at high temperatures. Weight loss data to 1000 hours exposure show the alkali resistance of the mats to be superior to that of asbestos.

  11. Hierarchically Porous Graphene as a Lithium-Air Battery Electrode

    SciTech Connect

    Xiao, Jie; Mei, Donghai; Li, Xiaolin; Xu, Wu; Wang, Deyu; Graff, Gordon L.; Bennett, Wendy D.; Nie, Zimin; Saraf, Laxmikant V.; Aksay, Ilhan A.; Liu, Jun; Zhang, Jiguang

    2011-11-09

    Functionalized graphene sheets (FGS) are successfully utilized as a novel air electrode for Li-O2 batteries. An extremely high capacity of 15,000 mAh/g was achieved by using the as-prepared graphene air electrode at a current density of 0.1 mA/cm2 in the pure oxygen environment. Although there is no pore in the two-dimensional FGS the as-prepared graphene air electrode consists of randomly arranged graphene nano-sheets which automatically form tunnels with different sizes. The large tunnels work as highways for the oxygen to quickly flow into the air electrode while the small pore-like tunnels can be considered as the numerous exits where the discharge products are accumulated. Combined with an appropriate electrolyte, the ideal discharge product Li2O2 is obtained without any carbonates byproducts in this system. Even when operated in ambient environment with a relative humidity of ~20% the specific capacity delivered from the pouch type cell achieves more than 5000 mAh/g making the graphene-based air electrode extremely attractive in the energy storage applications.

  12. Charging/discharging stability of a metal hydride battery electrode

    SciTech Connect

    Geng, M.; Han, J.; Feng, F.; Northwood, D.O.

    1999-07-01

    The metal hydride (MH) alloy powder for the negative electrode of the Ni/MH battery was first pulverized and oxidized by electrochemically charging and discharging for a number of cycles. The plate of the negative electrode of an experimental cell in this study was made from a mixture of a multicomponent AB{sub 5}-based alloy powder, nickel powder, and polytetra fluoroethylene (PTFE). The characteristics of the negative electrode, including discharge capacity, exchange current density, and hydrogen diffusivity, were studied by means of the electrochemical experiments and analysis in an experimental cell. The exchange current density of a Mm{sub 0.95}Ti{sub 0.05}Ni{sub 3.85}Co{sub 0.45}Mn{sub 0.35}Al{sub 0.35} alloy electrode increases with increasing number of charge/discharge cycles and then remains almost constant after 20 cycles. A microcracking activation, resulting from an increase in reaction surface area and an improvement in the electrode surface activation, increases the hydrogen exchange current densities. Measurement of hydrogen diffusivities for Mm{sub 0.95}Ti{sub 0.05}Ni{sub 3.85}Co{sub 0.45}Mn{sub 0.35}Al{sub 0.35} alloy powder shows that the ratio of D/a{sup 2} (D = hydrogen diffusivity; a = sphere radius) increases with increasing number of cycles but remains constant after 20 cycles.

  13. Laboratory study on the behaviour of spent AA household alkaline batteries in incineration

    SciTech Connect

    Almeida, Manuel F. Xara, Susana M.; Delgado, Julanda; Costa, Carlos A.

    2009-01-15

    The quantitative evaluation of emissions from incineration is essential when Life Cycle Assessment (LCA) studies consider this process as an end-of-life solution for some wastes. Thus, the objective of this work is to quantify the main gaseous emissions produced when spent AA alkaline batteries are incinerated. With this aim, batteries were kept for 1 h at 1273 K in a refractory steel tube hold in a horizontal electric furnace with temperature control. At one end of the refractory steel tube, a constant air flow input assures the presence of oxygen in the atmosphere and guides the gaseous emissions to a filter system followed by a set of two bubbler flasks having an aqueous solution of 10% (v/v) nitric acid. After each set of experiments, sulphur, chlorides and metals (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sb, Tl and Zn) were analyzed in both the solutions obtained from the steel tube washing and from the bubblers. Sulphur, chlorides and metals were quantified, respectively, using barium sulfate gravimetry, the Volhard method and atomic absorption spectrometry (AAS). The emissions of zinc, the most emitted metal, represent about 6.5% of the zinc content in the batteries. Emissions of manganese (whose oxide is the main component of the cathode) and iron (from the cathode collector) are negligible when compared with their amount in AA alkaline batteries. Mercury is the metal with higher volatility in the composition of the batteries and was collected even in the second bubbler flask. The amount of chlorides collected corresponds to about 36% of the chlorine in the battery sleeve that is made from PVC. A considerable part of the HCl formed in PVC plastic sleeve incineration is neutralized with KOH, zinc and manganese oxides and, thus, it is not totally released in the gas. Some of the emissions are predictable through a thermodynamic data analysis at temperatures in the range of 1200-1300 K taking into account the composition of the batteries. This analysis was done

  14. Laboratory study on the behaviour of spent AA household alkaline batteries in incineration.

    PubMed

    Almeida, Manuel F; Xará, Susana M; Delgado, Julanda; Costa, Carlos A

    2009-01-01

    The quantitative evaluation of emissions from incineration is essential when Life Cycle Assessment (LCA) studies consider this process as an end-of-life solution for some wastes. Thus, the objective of this work is to quantify the main gaseous emissions produced when spent AA alkaline batteries are incinerated. With this aim, batteries were kept for 1h at 1273K in a refractory steel tube hold in a horizontal electric furnace with temperature control. At one end of the refractory steel tube, a constant air flow input assures the presence of oxygen in the atmosphere and guides the gaseous emissions to a filter system followed by a set of two bubbler flasks having an aqueous solution of 10% (v/v) nitric acid. After each set of experiments, sulphur, chlorides and metals (As, Cd, Co, Cr, Cu, Fe, Hg, Mn, Ni, Pb, Sb, Tl and Zn) were analyzed in both the solutions obtained from the steel tube washing and from the bubblers. Sulphur, chlorides and metals were quantified, respectively, using barium sulfate gravimetry, the Volhard method and atomic absorption spectrometry (AAS). The emissions of zinc, the most emitted metal, represent about 6.5% of the zinc content in the batteries. Emissions of manganese (whose oxide is the main component of the cathode) and iron (from the cathode collector) are negligible when compared with their amount in AA alkaline batteries. Mercury is the metal with higher volatility in the composition of the batteries and was collected even in the second bubbler flask. The amount of chlorides collected corresponds to about 36% of the chlorine in the battery sleeve that is made from PVC. A considerable part of the HCl formed in PVC plastic sleeve incineration is neutralized with KOH, zinc and manganese oxides and, thus, it is not totally released in the gas. Some of the emissions are predictable through a thermodynamic data analysis at temperatures in the range of 1200-1300K taking into account the composition of the batteries. This analysis was done

  15. Phosphate glass electrode with good selectivity for alkaline-earth cations

    USGS Publications Warehouse

    Truesdell, A.H.; Pommer, A.M.

    1963-01-01

    A phosphate glass has been found to have a significant electrode specificity toward alkaline-earth ions. The order of selectivity is 2H + > Ba++ > Sr++ > Ca++ > 2K+ > 2Na+ > Mg++. Exchange properties are discussed in relation to possible structure. Its use to determine activity of Ca++ in natural systems containing Mg++ is suggested.

  16. Hydrophilic Electrode For An Alkaline Electrochemical Cell, And Method Of Manufacture

    DOEpatents

    Senyarich, Stephane; Cocciantelli, Jean-Michel

    2000-03-07

    A negative electrode for an alkaline electrochemical cell. The electrode comprises an active material and a hydrophilic agent constituted by small cylindrical rods of polyolefin provided with hydrophilic groups. The mean length of the rods is less than 50 microns and the mean diameter thereof is less than 20 microns. A method of manufacturing a negative electrode in which hydrophilic rods are made by fragmenting long polyolefin fibers having a mean diameter of less than 20 microns by oxidizing them, with the rods being mixed with the active material and the mixture being applied to a current conductor.

  17. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil

    2008-12-23

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2M'O.sub.3 in which 0batteries are disclosed with anode, cathode and electrolyte as are batteries of several cells connected in parallel or series or both.

  18. Lithium Metal Oxide Electrodes For Lithium Cells And Batteries

    DOEpatents

    Thackeray, Michael M.; Johnson, Christopher S.; Amine, Khalil; Kim, Jaekook

    2004-01-20

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0batteries are disclosed with anode, cathode and electrolyte as are batteries of several cells connected in parallel or series or both.

  19. Separator for alkaline electric batteries and method of making

    NASA Technical Reports Server (NTRS)

    Pfluger, H. L. (Inventor); Hoyt, H. E.

    1970-01-01

    Battery separator membranes of high electrolytic conductivity comprising a cellulose ether and a compatible metallic salt of water soluble aliphatic acids and their hydroxy derivatives are described. It was found that methyl cellulose can be modified by another class of materials, nonpolymeric in nature, to form battery separator membranes of low electrolytic resistance but which have the flexibility of membranes made of unmodified methyl cellulose, and which in many cases enhance flexibility over membranes made with unmodified methyl cellulose. Separator membranes for electrochemical cells comprising a cellulose ether and a modified selected from the group consisting of metallic salts of water soluble alphatic acids and their hydroxy derivatives and to electrochemical cells utilizing said membranes are described.

  20. Performance Enhancement and Side Reactions in Rechargeable Nickel-Iron Batteries with Nanostructured Electrodes.

    PubMed

    Lei, Danni; Lee, Dong-Chan; Magasinski, Alexandre; Zhao, Enbo; Steingart, Daniel; Yushin, Gleb

    2016-01-27

    We report for the first time a solution-based synthesis of strongly coupled nanoFe/multiwalled carbon nanotube (MWCNT) and nanoNiO/MWCNT nanocomposite materials for use as anodes and cathodes in rechargeable alkaline Ni-Fe batteries. The produced aqueous batteries demonstrate very high discharge capacities (800 mAh gFe(-1) at 200 mA g(-1) current density), which exceed that of commercial Ni-Fe cells by nearly 1 order of magnitude at comparable current densities. These cells also showed the lack of any "activation", typical in commercial batteries, where low initial capacity slowly increases during the initial 20-50 cycles. The use of a highly conductive MWCNT network allows for high-capacity utilization because of rapid and efficient electron transport to active metal nanoparticles in oxidized [such as Fe(OH)2 or Fe3O4] states. The flexible nature of MWCNTs accommodates significant volume changes taking place during phase transformation accompanying reduction-oxidation reactions in metal electrodes. At the same time, we report and discuss that high surface areas of active nanoparticles lead to multiple side reactions. Dissolution of Fe anodes leads to reprecipitation of significantly larger anode particles. Dissolution of Ni cathodes leads to precipitation of Ni metal on the anode, thus blocking transport of OH(-) anions. The electrolyte molarity and composition have a significant impact on the capacity utilization and cycling stability. PMID:26720271

  1. Development of a benchmarking model for lithium battery electrodes

    NASA Astrophysics Data System (ADS)

    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.

  2. FeS/C composite as high-performance anode material for alkaline nickel-iron rechargeable batteries

    NASA Astrophysics Data System (ADS)

    Shangguan, Enbo; Li, Fei; Li, Jing; Chang, Zhaorong; Li, Quanmin; Yuan, Xiao-Zi; Wang, Haijiang

    2015-09-01

    FeS and its composite, FeS/C, are synthesized via a simple calcination method followed by a co-precipitation process. The electrochemical properties of the bare FeS and FeS/C composite as anode materials for alkaline nickel-iron batteries are investigated. The results show that the FeS/C-3wt%Bi2O3-mixed electrode delivers a high specific capacity of 325 mAh g-1 at a current density of 300 mA g-1 with a faradaic efficiency of 90.3% and retains 99.2% of the initial capacity after 200 cycles. For the first time, it is demonstrated that even at a discharge rate as high as 1500 mA g-1 (5C) the FeS/C-3wt%Bi2O3-mixed electrode delivers a specific capacity of nearly 230 mAh g-1. SEM results confirm that after 200 discharge-charge cycles, the size of FeS/C particles reduces from 5 to 15 μm to less than 300 nm in diameter and the particles are highly dispersed on the surface of carbon black, which is likely caused by the dissolution-deposition process of Fe(OH)2 and Fe via intermediate iron species. As a result, the FeS/C composite exhibits considerably high charge efficiency, high discharge capacities, excellent rate capability and superior cycling stability. We believe that this composite is a potential candidate of high-performance anode materials for alkaline iron-based rechargeable batteries.

  3. Electrode performance of romanechite for rechargeable lithium batteries

    NASA Astrophysics Data System (ADS)

    Tsuda, Masayuki; Arai, Hajime; Nemoto, Yasue; Sakurai, Yoji

    We studied romanechite, (2×3) tunnel type manganese dioxide, as a positive electrode material for rechargeable lithium batteries. We synthesized the sample by soft chemical techniques, and its chemical composition was Ba 0.18MnO 2.10·0.42H 2O. We obtained a first discharge capacity of 120 mAh g -1 (energy density 264 mWh g -1). The capacity decreased with cycling. We examined the thermal behavior of this material, revealing its high thermal stability.

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

    SciTech Connect

    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

  5. Polypyrrole composite electrodes in an all-polymer battery system

    SciTech Connect

    Killian, J.G.; Coffey, B.M.; Gao, F.; Poehler, T.O.; Searson, P.C.

    1996-03-01

    The authors have fabricated an all-polymer battery utilizing the redox properties of electrically conducting polymers for the anode and cathode in conjunction with an ionic conducting polymer gel electrolyte. The anode and cathode consist of pyrrole electropolymerized onto a graphite fiber substrate resulting in a high-surface-area, composite electrode. A polymer gel electrolyte, based on polyacrylonitrile, was solution cast onto the electrodes to form an all-polymer cell. This system exhibits a specific charge capacity of 22 mAh/g based on the electroactive mass of the cathode and discharging the system to 0.4 V. These cells show no loss of capacity when cycled to 100 cycles.

  6. Ionic Conduction in Lithium Ion Battery Composite Electrode Governs Cross-sectional Reaction Distribution

    PubMed Central

    Orikasa, Yuki; Gogyo, Yuma; Yamashige, Hisao; Katayama, Misaki; Chen, Kezheng; Mori, Takuya; Yamamoto, Kentaro; Masese, Titus; Inada, Yasuhiro; Ohta, Toshiaki; Siroma, Zyun; Kato, Shiro; Kinoshita, Hajime; Arai, Hajime; Ogumi, Zempachi; Uchimoto, Yoshiharu

    2016-01-01

    Composite electrodes containing active materials, carbon and binder are widely used in lithium-ion batteries. Since the electrode reaction occurs preferentially in regions with lower resistance, reaction distribution can be happened within composite electrodes. We investigate the relationship between the reaction distribution with depth direction and electronic/ionic conductivity in composite electrodes with changing electrode porosities. Two dimensional X-ray absorption spectroscopy shows that the reaction distribution is happened in lower porosity electrodes. Our developed 6-probe method can measure electronic/ionic conductivity in composite electrodes. The ionic conductivity is decreased for lower porosity electrodes, which governs the reaction distribution of composite electrodes and their performances. PMID:27193448

  7. Ionic Conduction in Lithium Ion Battery Composite Electrode Governs Cross-sectional Reaction Distribution

    NASA Astrophysics Data System (ADS)

    Orikasa, Yuki; Gogyo, Yuma; Yamashige, Hisao; Katayama, Misaki; Chen, Kezheng; Mori, Takuya; Yamamoto, Kentaro; Masese, Titus; Inada, Yasuhiro; Ohta, Toshiaki; Siroma, Zyun; Kato, Shiro; Kinoshita, Hajime; Arai, Hajime; Ogumi, Zempachi; Uchimoto, Yoshiharu

    2016-05-01

    Composite electrodes containing active materials, carbon and binder are widely used in lithium-ion batteries. Since the electrode reaction occurs preferentially in regions with lower resistance, reaction distribution can be happened within composite electrodes. We investigate the relationship between the reaction distribution with depth direction and electronic/ionic conductivity in composite electrodes with changing electrode porosities. Two dimensional X-ray absorption spectroscopy shows that the reaction distribution is happened in lower porosity electrodes. Our developed 6-probe method can measure electronic/ionic conductivity in composite electrodes. The ionic conductivity is decreased for lower porosity electrodes, which governs the reaction distribution of composite electrodes and their performances.

  8. Ionic Conduction in Lithium Ion Battery Composite Electrode Governs Cross-sectional Reaction Distribution.

    PubMed

    Orikasa, Yuki; Gogyo, Yuma; Yamashige, Hisao; Katayama, Misaki; Chen, Kezheng; Mori, Takuya; Yamamoto, Kentaro; Masese, Titus; Inada, Yasuhiro; Ohta, Toshiaki; Siroma, Zyun; Kato, Shiro; Kinoshita, Hajime; Arai, Hajime; Ogumi, Zempachi; Uchimoto, Yoshiharu

    2016-01-01

    Composite electrodes containing active materials, carbon and binder are widely used in lithium-ion batteries. Since the electrode reaction occurs preferentially in regions with lower resistance, reaction distribution can be happened within composite electrodes. We investigate the relationship between the reaction distribution with depth direction and electronic/ionic conductivity in composite electrodes with changing electrode porosities. Two dimensional X-ray absorption spectroscopy shows that the reaction distribution is happened in lower porosity electrodes. Our developed 6-probe method can measure electronic/ionic conductivity in composite electrodes. The ionic conductivity is decreased for lower porosity electrodes, which governs the reaction distribution of composite electrodes and their performances. PMID:27193448

  9. An unusual electrical burn caused by alkaline batteries.

    PubMed

    Roan, Tyng-Luen; Yeong, Eng-Kean; Tang, Yueh-Bih

    2015-02-01

    Electrical burns caused by low-voltage batteries are rarely reported. We recently encountered a male patient who suffered from a superficial second-degree burn over his left elbow and back. The total body surface area of the burn was estimated to be 6%. After interviewing the patient, the cause was suspected to be related to the explosion of a music player on the left-side of his waist, carried on his belt while he was painting a bathroom wall. Elevated creatine kinase levels and hematuria indicated rhabdomyolysis and suggested an electrical burn. Initial treatment was done in the burn intensive care unit with fluid challenge and wound care. The creatine kinase level decreased gradually and the hematuria was gone after 4 days in the intensive care unit. He was then transferred to the general ward for further wound management and discharged from our burn center after a total of 11 days without surgical intervention. PMID:25678181

  10. Factors influence flexibility resistivity and zinc dendrite penetration rate of inorganic separators for alkaline batteries

    NASA Technical Reports Server (NTRS)

    Sheibley, D. W.

    1975-01-01

    Developmental work resulted in a formulation which can improve the flexibility of the inorganic-organic-type separator for silver-zinc and nickel-zinc alkaline batteries. The effects of various fillers and reactive organic additives on separator volume resistivity are described. The effects of various inert fillers on the zinc dendrite penetration rate of the separator are shown. Conclusions regarding the operating mechanism of the separator are presented.

  11. Seeking effective dyes for a mediated glucose-air alkaline battery/fuel cell

    NASA Astrophysics Data System (ADS)

    Eustis, Ross; Tsang, Tsz Ming; Yang, Brigham; Scott, Daniel; Liaw, Bor Yann

    2014-02-01

    A significant level of power generation from an abiotic, air breathing, mediated reducing sugar-air alkaline battery/fuel cell has been achieved in our laboratories at room temperature without complicated catalysis or membrane separation in the reaction chamber. Our prior studies suggested that mass transport limitation by the mediator is a limiting factor in power generation. New and effective mediators were sought here to improve charge transfer and power density. Forty-five redox dyes were studied to identify if any can facilitate mass transport in alkaline electrolyte solution; namely, by increasing the solubility and mobility of the dye, and the valence charge carried per molecule. Indigo dyes were studied more closely to understand the complexity involved in mass transport. The viability of water-miscible co-solvents was also explored to understand their effect on solubility and mass transport of the dyes. Using a 2.0 mL solution, 20% methanol by volume, with 100 mM indigo carmine, 1.0 M glucose and 2.5 M sodium hydroxide, the glucose-air alkaline battery/fuel cell attained 8 mA cm-2 at short-circuit and 800 μW cm-2 at the maximum power point. This work shall aid future optimization of mediated charge transfer mechanism in batteries or fuel cells.

  12. Polyphase alloys as rechargeable electrodes in advanced battery systems

    NASA Technical Reports Server (NTRS)

    Huggins, Robert A.

    1987-01-01

    The rechargeability of electrochemical cells is often limited by negative electrode problems. These may include loss of capacity, increased impedance, macroscopic shape change, dendrite growth, or a tendency for filamentary or whisker growth. In principle, these problems can be reduced or eliminated by the use of alloys that undergo either displacement or insertion reactions at reactant species activities less than unity, rather than pure elements. The fundamental reasons for some of these problems with elemental electrodes, as well as the basic principles involved in the different behavior of alloys, are briefly discussed. More information is now available concerning the thermodynamic and kinetic properties of a number of alloys of potential interest for use as electrodes in elevated temperature lithium battery systems. Recent results have extended these results down to ambient temperatures, indicating that some such materials may be of interest for use with new low temperature molten salt electrolytes, or with organic solvent electrolytes. The all solid mixed conductor matrix concept is also reviewed.

  13. All-solid-state Al-air batteries with polymer alkaline gel electrolyte

    NASA Astrophysics Data System (ADS)

    Zhang, Zhao; Zuo, Chuncheng; Liu, Zihui; Yu, Ying; Zuo, Yuxin; Song, Yu

    2014-04-01

    Aluminum-air (Al-air) battery is one of the most promising candidates for next-generation energy storage systems because of its high capacity and energy density, and abundance. The polyacrylic acid (PAA)-based alkaline gel electrolyte is used in all-solid-state Al-air batteries instead of aqueous electrolytes to prevent leakage. The optimal gel electrolyte exhibits an ionic conductivity of 460 mS cm-1, which is close to that of aqueous electrolytes. The Al-air battery peak capacity and energy density considering only Al can reach 1166 mAh g-1-Al and 1230 mWh g-1-Al, respectively, during constant current discharge. The battery prototype also exhibits a high power density of 91.13 mW cm-2. For the battery is a laminated structure, area densities of 29.2 mAh cm-2 and 30.8 mWh cm-2 are presented to appraise the performance of the whole cell. A novel design to inhibit anodic corrosion is proposed by separating the Al anode from the gel electrolyte when not in use, thereby effectively maintaining the available capacity of the battery.

  14. Surface functionality and electrochemical investigations of a graphitic electrode as a candidate for alkaline energy conversion and storage devices

    NASA Astrophysics Data System (ADS)

    Soliman, Ahmed B.; Abdel-Samad, Hesham S.; Abdel Rehim, Sayed S.; Hassan, Hamdy H.

    2016-02-01

    Graphite is a typical electrocatalyst support in alkaline energy conversion and storage devices such as fuel cells, supercapacitores and lithium ion batteries. The electrochemical behaviour of a graphite electrode in 0.5 M NaOH was studied to elucidate its surface structure/electrochemical activity relationship. Graphite voltammograms are characterized by an anodic shoulder AI and a cathodic peak CI in addition to the oxygen reduction reaction plateaus, PI and PII. AI and CI were attributed to oxidation and reduction of some graphite surface function groups, respectively. Rotating ring disk electrode (RRDE) study revealed two different oxygen types assigned as inner and outer oxygen. The inner oxygen was reduced via the more efficient 4-electron pathway. The outer oxygen reduction proceeded with a lower efficient 2-electron pathway. The calculated percentages of the 4-electron pathway were ranged from 70% to 90%. A full mechanism for the graphite surface function groups changes over the studied potential window was suggested through the combination between the voltammetric, FT-IR and Raman results.

  15. Surface functionality and electrochemical investigations of a graphitic electrode as a candidate for alkaline energy conversion and storage devices

    PubMed Central

    Soliman, Ahmed B.; Abdel-Samad, Hesham S.; Abdel Rehim, Sayed S.; Hassan, Hamdy H.

    2016-01-01

    Graphite is a typical electrocatalyst support in alkaline energy conversion and storage devices such as fuel cells, supercapacitores and lithium ion batteries. The electrochemical behaviour of a graphite electrode in 0.5 M NaOH was studied to elucidate its surface structure/electrochemical activity relationship. Graphite voltammograms are characterized by an anodic shoulder AI and a cathodic peak CI in addition to the oxygen reduction reaction plateaus, PI and PII. AI and CI were attributed to oxidation and reduction of some graphite surface function groups, respectively. Rotating ring disk electrode (RRDE) study revealed two different oxygen types assigned as inner and outer oxygen. The inner oxygen was reduced via the more efficient 4-electron pathway. The outer oxygen reduction proceeded with a lower efficient 2-electron pathway. The calculated percentages of the 4-electron pathway were ranged from 70% to 90%. A full mechanism for the graphite surface function groups changes over the studied potential window was suggested through the combination between the voltammetric, FT-IR and Raman results. PMID:26916054

  16. Surface functionality and electrochemical investigations of a graphitic electrode as a candidate for alkaline energy conversion and storage devices.

    PubMed

    Soliman, Ahmed B; Abdel-Samad, Hesham S; Abdel Rehim, Sayed S; Hassan, Hamdy H

    2016-01-01

    Graphite is a typical electrocatalyst support in alkaline energy conversion and storage devices such as fuel cells, supercapacitores and lithium ion batteries. The electrochemical behaviour of a graphite electrode in 0.5 M NaOH was studied to elucidate its surface structure/electrochemical activity relationship. Graphite voltammograms are characterized by an anodic shoulder AI and a cathodic peak CI in addition to the oxygen reduction reaction plateaus, PI and PII. AI and CI were attributed to oxidation and reduction of some graphite surface function groups, respectively. Rotating ring disk electrode (RRDE) study revealed two different oxygen types assigned as inner and outer oxygen. The inner oxygen was reduced via the more efficient 4-electron pathway. The outer oxygen reduction proceeded with a lower efficient 2-electron pathway. The calculated percentages of the 4-electron pathway were ranged from 70% to 90%. A full mechanism for the graphite surface function groups changes over the studied potential window was suggested through the combination between the voltammetric, FT-IR and Raman results. PMID:26916054

  17. Development and testing of an economic grid-scale flow-assisted zinc/nickel-hydroxide alkaline battery

    NASA Astrophysics Data System (ADS)

    Turney, Damon E.; Shmukler, Michael; Galloway, Kevin; Klein, Martin; Ito, Yasumasa; Sholklapper, Tal; Gallaway, Joshua W.; Nyce, Michael; Banerjee, Sanjoy

    2014-10-01

    An economic design for an alkaline zinc-anode flow-assisted battery without membrane separators was tested at grid-scale of 25 kWh with a string of thirty 833 Wh cells in series, and also at bench scale with individual 28 Wh cells. The bench-scale tests allowed optimization of parameters such as electrolyte flow, choice of hardware material, electrolyte composition, and charge/discharge protocol. The best-performing bench scale cell cycled for over 3300 cycles with energy efficiency above 80%, and was selected as the design basis for scale-up to the 25 kWh battery string. Testing of the grid-scale string demonstrated 1000+ cycles with round trip energy efficiency above 80%. Two challenges observed at the bench scale were overcome for successful scale-up, namely a) passivation of the anode surface, which occurred when the anode experienced voltages 100 mV above zinc's rest voltage, and b) zinc particulates that jammed the gap between the electrodes and caused cathode degradation and passivation of the anode surface. Best practices to overcome these challenges and achieve long cycle life are presented.

  18. Workshop on electrodes for flowing solution batteries. Summary report

    SciTech Connect

    Nanis, L.

    1981-02-01

    The electrochemical technology of aqueous secondary cells with flowing electrolyte solutions was the subject of a workshop sponsored by EPRI with the cooperation of DOE. The workshop was held in Tampa, Florida, 5-7 November 1979, and was attended by a select group drawn from advanced battery developers, government agencies, universities, and research organizations. The workshop general objectives were to look at the significant parameters believed to govern the performance of the two basic types of electrodes now in use; namely, a porous flow-through electrode (PFTE), and an impervious flow-by electrode. Progress, problems, and prospects were informally discussed. Brief critical reviews were given by session chairmen as a means of introducing each of the key topics (Current Distribution in FTPE, Conversion Efficiency, Segmented FTPE Studies, General Discussion on FTPF Parameters, Surface Activation, Application of FTPE to Waste Recovery, Exxon Zinc-Bromine Flow-By System, FTPE In NASA Redox Energy Storage, and Application of FTPE In Lockheed Zinc/Ferricyanide Redox System). The interaction of this diverse group of engineers and scientists was said by all to be of great benefit in widening understanding of the problems and possible future approaches to new work. The main needs for future work that were identified in the final discussion session among the participants were: (1) engineering analysis, (2) porous structures, (3) materials characteristics, and (4) chemical characteristics. In generally comparing flow-through to flow-by electrodes, there were some surprising differences arising from experimental results that did not fit conventional thinking.

  19. Evaluation residual moisture in lithium-ion battery electrodes and its effect on electrode performance

    DOE PAGESBeta

    Li, Jianlin; Daniel, Claus; Wood, III, David L.; An, Seong Jin

    2016-01-11

    Removing residual moisture in lithium-ion battery electrodes is essential for desired electrochemical performance. In this manuscript, the residual moisture in LiNi0.5Mn0.3Co0.2O2 cathodes produced by conventional solvent-based and aqueous processing is characterized and compared. The electrochemical performance has also been investigated for various residual moisture contents. As a result, it has been demonstrated that the residual moisture lowers the first cycle coulombic efficiency, but its effect on short term cycle life is insignificant.

  20. Alkaline battery containing a separator of a cross-linked copolymer of vinyl alcohol and unsaturated carboxylic acid

    NASA Technical Reports Server (NTRS)

    Hsu, L. C.; Philipp, W. H.; Sheibley, D. W.; Gonzalez-Sanabria, O. D. (Inventor)

    1985-01-01

    A battery separator for an alkaline battery is described. The separator comprises a cross linked copolymer of vinyl alcohol units and unsaturated carboxylic acid units. The cross linked copolymer is insoluble in water, has excellent zincate diffusion and oxygen gas barrier properties and a low electrical resistivity. Cross linking with a polyaldehyde cross linking agent is preferred.

  1. Synthesis of Graphene from a Used Battery Electrode

    NASA Astrophysics Data System (ADS)

    Kumar, M. K. Punith; Srivastava, Chandan

    2016-01-01

    Graphene was produced by electrochemical exfoliation of a used battery electrode. Aqueous solutions of cationic (cetyltrimethylammonium bromide), anionic (sodium dodecyl sulphate), and nonionic (poly vinyl pyrrolidone) surfactants, along with NaCl and combinations of these surfactants with NaCl, were used as the electrolyte. The following observations were made: (I) up to several micrometer sized graphene sheets were produced, (II) the addition of NaCl into the electrolytes significantly enhanced the yield of the exfoliated graphene, (III) the type of surfactant affected the defect density of the exfoliated product, and (IV) electrochemical impedance spectroscopy provided insight into the reason for the changes in the defect density ratio between the graphene samples.

  2. Charge control of nickel-cadmium batteries by coulometer and third electrode method

    NASA Technical Reports Server (NTRS)

    Ford, F.; Paulkovitch, J.

    1968-01-01

    Combined coulometer/third electrode control circuit for a nickel-cadmium battery included at least one cell of the third electrode type is illustrated. The coulometer/third electrode sensing circuit controls the series regulator as necessary to maintain the sensing voltage at the preset sensing level.

  3. Real-time materials evolution visualized within intact cycling alkaline batteries

    SciTech Connect

    Gallaway, JW; Erdonmez, CK; Zhong, Z; Croft, M; Sviridov, LA; Sholklapper, TZ; Turney, DE; Banerjee, S; Steingart, DA

    2014-01-01

    The scientific community has focused on the problem of inexpensive, safe, and sustainable large-scale electrical energy storage, which is needed for a number of emerging societal reasons such as stabilizing intermittent renewables-based generation like solar and wind power. The materials used for large-scale storage will need to be low cost, earth-abundant, and safe at the desired scale. The Zn-MnO2 "alkaline" battery chemistry is associated with one-time use, despite being rechargeable. This is due to material irreversibilities that can be triggered in either the anode or cathode. However, as Zn and MnO2 have high energy density and low cost, they are economically attractive even at limited depth of discharge. As received, a standard bobbin-type alkaline cell costs roughly $20 per kW h. The U. S. Department of Energy ARPA-E $100 per kW h cost target for grid storage is thus close to the cost of alkaline consumer primary cells if re-engineered and/or cycled at 5-20% nominal capacity. Herein we use a deeply-penetrating in situ technique to observe ZnO precipitation near the separator in an alkaline cell anode cycled at 5% DOD, which is consistent with cell failures observed at high cycle life. Alkaline cells designed to avoid such causes of cell failure could serve as a low-cost baseload for large-scale storage.

  4. Hierarchical Co@C Nanoflowers: Synthesis and Electrochemical Properties as an Advanced Negative Material for Alkaline Secondary Batteries.

    PubMed

    Li, Li; Ma, Jianmin; Zhang, Zichao; Cao, Bingqiang; Wang, Yijing; Jiao, Lifang; Yuan, Huatang

    2015-11-01

    Hierarchical Co@C nanoflowers have been facilely synthesized via a simple route based on a low-temperature solid-phase reaction. The obtained hierarchical Co@C nanoflowers, each constructed of a number of nanosheets, display a three-dimensional architecture with an average grain size of about 300 nm. The electrochemical properties of the Co@C nanoflowers as the negative material for Ni/Co cells have been systemically researched. In particular, Co@C material exhibits high discharge-specific capacity and good cycling stability. The discharge-specific capacity of our Co@C-3 electrode can reach 612.1 mA h g(-1), and the specific capacity of 415.3 mA h g(-1) is retained at a current density of 500 mA g(-1) after 120 cycles, indicating its great potential for high-performance Ni/Co batteries. Interestingly, the as-synthesized Co@C electrode also exhibits favorable rate capability. These desirable properties can be attributed to porous pathways, which allow fast transportation of ions and electrons and easy accessibility to the electrolyte. The dominant electrochemical mechanism of Co@C can be attributed to the reduction-oxidation reaction between metallic cobalt and cobalt hydroxide in alkaline solution. PMID:26460934

  5. Electrocatalytic Activity of Transition Metal Oxide-Carbon Composites for Oxygen Reduction in Alkaline Batteries and Fuel Cells

    SciTech Connect

    Malkhandi, S; Trinh, P; Manohar, AK; Jayachandrababu, KC; Kindler, A; Prakash, GKS; Narayanan, SR

    2013-06-07

    Conductive transition metal oxides (perovskites, spinels and pyrochlores) are attractive as catalysts for the air electrode in alkaline rechargeable metal-air batteries and fuel cells. We have found that conductive carbon materials when added to transition metal oxides such as calcium-doped lanthanum cobalt oxide, nickel cobalt oxide and calcium-doped lanthanum manganese cobalt oxide increase the electrocatalytic activity of the oxide for oxygen reduction by a factor of five to ten. We have studied rotating ring-disk electrodes coated with (a) various mass ratios of carbon and transition metal oxide, (b) different types of carbon additives and (c) different types of transition metal oxides. Our experiments and analysis establish that in such composite catalysts, carbon is the primary electro- catalyst for the two-electron electro-reduction of oxygen to hydroperoxide while the transition metal oxide decomposes the hydroperoxide to generate additional oxygen that enhances the observed current resulting in an apparent four-electron process. These findings are significant in that they change the way we interpret previous reports in the scientific literature on the electrocatalytic activity of various transition metal oxide- carbon composites for oxygen reduction, especially where carbon is assumed to be an additive that just enhances the electronic conductivity of the oxide catalyst. (C) 2013 The Electrochemical Society. All rights reserved.

  6. Progress towards high-power Li/CFx batteries: electrode architectures using carbon nanotubes with CFx.

    PubMed

    Zhang, Qing; Takeuchi, Kenneth J; Takeuchi, Esther S; Marschilok, Amy C

    2015-09-21

    Carbon monofluoride (CFx) has a high energy density, exceeding 2000 W h kg(-1), yet its application in primary lithium batteries is limited by its power capability. Multi-walled carbon nanotubes (CNTs) are appealing additives for high-power batteries, due to their outstanding electronic transport properties, high aspect ratio necessitating low volume fraction for percolation, and high tensile strength. This perspective describes the current state of the art in lithium-carbon monofluoride (Li/CFx) batteries and highlights the opportunities for the development of high-power Li/CFx batteries via utilization of carbon nanotubes. In this report, we generated several electrode architectures using CFx/CNT combinations, and demonstrated the effectiveness of CNTs in enhancing the rate capability and energy density of Li/CFx batteries. First, we investigated the resistivity of CFx combined with CNTs and compared the CFx/CNT composites with conventional carbon additives. Second, we built CFx-CNT electrodes without metallic current collectors using CNTs as substrates, and compared their electrochemical performance with conventional CFx electrodes using aluminum foil as a current collector. Furthermore, we fabricated multi-layered CNT-CFx-CNT composite electrodes (sandwich electrodes) and studied the impact of the structure on the performance of the electrode. Our work demonstrates some of the opportunities for utilization of CNTs in CFx electrodes and the resultant implementation of CFx as a battery cathode in next-generation high-power batteries. PMID:26280394

  7. The relationship between coefficient of restitution and state of charge of zinc alkaline primary LR6 batteries [Bouncing alkaline batteries: A basic solution

    SciTech Connect

    Bhadra, S.; Hertzberg, B. J.; Croft, M.; Gallaway, J. W.; Van Tassell, B. J.; Chamoun, M.; Erdonmez, C.; Zhong, Z.; Steingart, D. A.

    2015-03-13

    The coefficient of restitution of alkaline batteries had been shown to increase as a function of depth of discharge. In this work, using non-destructive mechanical testing, the change in coefficient of restitution is compared to in situ energy-dispersive x-ray diffraction data to determine the cause of the macroscopic change in coefficient of restitution. The increase in coefficient of restitution correlates to the formation of a percolation pathway of ZnO within the anode of the cell, and that the coefficient of restitution saturates at a value of 0.63 ± .05 at 50% state if charge when the anode has densified into porous ZnO solid. Of note is the sensitivity of coefficient of restitution to the amount of ZnO formation that rivals the sensitivity on in situ energy-dispersive x-ray diffraction spectroscopy.

  8. The relationship between coefficient of restitution and state of charge of zinc alkaline primary LR6 batteries [Bouncing alkaline batteries: A basic solution

    DOE PAGESBeta

    Bhadra, S.; Hertzberg, B. J.; Croft, M.; Gallaway, J. W.; Van Tassell, B. J.; Chamoun, M.; Erdonmez, C.; Zhong, Z.; Steingart, D. A.

    2015-03-13

    The coefficient of restitution of alkaline batteries had been shown to increase as a function of depth of discharge. In this work, using non-destructive mechanical testing, the change in coefficient of restitution is compared to in situ energy-dispersive x-ray diffraction data to determine the cause of the macroscopic change in coefficient of restitution. The increase in coefficient of restitution correlates to the formation of a percolation pathway of ZnO within the anode of the cell, and that the coefficient of restitution saturates at a value of 0.63 ± .05 at 50% state if charge when the anode has densified intomore » porous ZnO solid. Of note is the sensitivity of coefficient of restitution to the amount of ZnO formation that rivals the sensitivity on in situ energy-dispersive x-ray diffraction spectroscopy.« less

  9. Electrochromic & magnetic properties of electrode materials for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Zheng-Fei, Guo; Kun, Pan; Xue-Jin, Wang

    2016-01-01

    Progress in electrochromic lithium ion batteries (LIBs) is reviewed, highlighting advances and possible research directions. Methods for using the LIB electrode materials’ magnetic properties are also described, using several examples. Li4Ti5O12 (LTO) film is discussed as an electrochromic material and insertion compound. The opto-electrical properties of the LTO film have been characterized by electrical measurements and UV-Vis spectra. A prototype bi-functional electrochromic LIB, incorporating LTO as both electrochromic layer and anode, has also been characterized by charge- discharge measurements and UV-Vis transmittance. The results show that the bi-functional electrochromic LIB prototype works well. Magnetic measurement has proven to be a powerful tool to evaluate the quality of electrode materials. We introduce briefly the magnetism of solids in general, and then discuss the magnetic characteristics of layered oxides, spinel oxides, olivine phosphate LiFePO4, and Nasicon-type Li3Fe2(PO4)3. We also discuss what kind of impurities can be detected, which will guide us to fabricate high quality films and high performance devices. Project supported by the National High Technology Research and Development Program of China (Grant No. 2015AA034201) and the Chinese Universities Scientific Fund (Grant No. 2015LX002).

  10. Prismatic sealed nickel-cadmium batteries utilizing fiber structured electrodes. II - Applications as a maintenance free aircraft battery

    NASA Astrophysics Data System (ADS)

    Anderman, Menahem; Benczur-Urmossy, Gabor; Haschka, Friedrich

    Test data on prismatic sealed Ni-Cd batteries utilizing fiber structured electrodes (sealed FNC) is discussed. It is shown that, under a voltage limited charging scheme, the charge acceptance of the sealed FNC battery is far superior to that of the standard vented aircraft Ni-Cd batteries. This results in the sealed FNC battery maintaining its capacity over several thousand cycles without any need for electrical conditioning or water topping. APU start data demonstrate superior power capabilities over existing technologies. Performance at low temperature is presented. Abuse test results reveal a safe fail mechanism even under severe electrical abuse.

  11. Application of Carbon Nanomaterials in Lithium-Ion Battery Electrodes

    NASA Astrophysics Data System (ADS)

    Jaber-Ansari, Laila

    Carbon nanomaterials such as single-walled carbon nanotubes (SWCNTs) and graphene have emerged as leading additives for high capacity nanocomposite lithium ion battery electrodes due to their ability to improve electrode conductivity, current collection efficiency, and charge/discharge rate for high power applications. In this work, the these nanomaterials have been developed and their properties have been fine-tuned to help solve fundamental issues in conventional lithium ion battery electrodes. Towards this end, the application of SWCNTs in lithium-ion anodes has been studied. As-grown SWCNTs possess a distribution of physical and electronic structures, and it is of high interest to determine which subpopulations of SWCNTs possess the highest lithiation capacity and to develop processing methods that can enhance the lithiation capacity of underperforming SWCNT species. Towards this end, SWCNT electronic type purity is controlled via density gradient ultracentrifugation, enabling a systematic study of the lithiation of SWCNTs as a function of metal versus semiconducting content. Experimentally, vacuum filtered freestanding films of metallic SWCNTs are found to accommodate lithium with an order of magnitude higher capacity than their semiconducting counterparts. In contrast, SWCNT film densification leads to the enhancement of the lithiation capacity of semiconducting SWCNTs to levels comparable to metallic SWCNTs, which is corroborated by theoretical calculations. To understand the interaction of the graphene with lithium ions and electrolyte species during electrochemical we use Raman spectroscopy in a model system of monolayer graphene transferred on a Si(111) substrate and density functional theory (DFT) to investigate defect formation as a function of lithiation. This model system enables the early stages of defect formation to be probed in a manner previously not possible with commonly-used reduced graphene oxide or multilayer graphene substrates. Using ex

  12. Mechanics of high-capacity electrodes in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Ting, Zhu

    2016-01-01

    Rechargeable batteries, such as lithium-ion batteries, play an important role in the emerging sustainable energy landscape. Mechanical degradation and resulting capacity fade in high-capacity electrode materials critically hinder their use in high-performance lithium-ion batteries. This paper presents an overview of recent advances in understanding the electrochemically-induced mechanical behavior of the electrode materials in lithium-ion batteries. Particular emphasis is placed on stress generation and facture in high-capacity anode materials such as silicon. Finally, we identify several important unresolved issues for future research. Project support by the NSF (Grant Nos. CMMI 1100205 and DMR 1410936).

  13. Improved Positive Electrode Materials for Lithium-ion Batteries

    NASA Astrophysics Data System (ADS)

    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, Li

  14. Life cycle assessment of three different management options for spent alkaline batteries.

    PubMed

    Xará, Susana; Almeida, Manuel Fonseca; Costa, Carlos

    2015-09-01

    The potential environmental impact of Landfilling, Incineration and Recycling of spent household alkaline batteries collected in continental Portugal was compared using LCA methodology and the Recipe Impact Assessment method. Major contributors and improvement opportunities for each system were identified and scenarios for 2012 and 2016 legislation targets were evaluated. For 13 out of the 18 impact categories, the Recycling system is the worst alternative, Incineration is the worst option for 4 and Landfill is the worst option only for one impact category. However if additionally in each system the recovery of materials and energy is taken into account there is a noticeable advantage of the Recycling system for all the impact categories. The environmental profiles for 2012 and 2016 scenarios (25% and 45% recycling rates, respectively) show the dominance of the Recycling system for most of the impact categories. Based on the results of this study, it is questioned whether there are environmental benefits of recycling abroad the household alkaline batteries collected in continental Portugal and, since the low environmental performance of the Recycling system is particularly due to the international transport of the batteries to the recycling plant, is foreseen that a recycling facility located in Portugal, could bring a positive contribution to the environmental impact of the legislation compliance. PMID:26119009

  15. Process for the recycling of alkaline and zinc-carbon spent batteries

    NASA Astrophysics Data System (ADS)

    Ferella, Francesco; De Michelis, Ida; Vegliò, Francesco

    In this paper a recycling process for the recovery of zinc and manganese from spent alkaline and zinc-carbon batteries is proposed. Laboratory tests are performed to obtain a purified pregnant solution from which metallic zinc (purity 99.6%) can be recovered by electrolysis; manganese is recovered as a mixture of oxides by roasting of solid residue coming from the leaching stage. Nearly 99% of zinc and 20% of manganese are extracted after 3 h, at 80 °C with 10% w/v pulp density and 1.5 M sulphuric acid concentration. The leach liquor is purified by a selective precipitation of iron, whereas metallic impurities, such as copper, nickel and cadmium are removed by cementation with zinc powder. The solid residue of leaching is roasted for 30 min at 900 °C, removing graphite completely and obtaining a mixture of Mn 3O 4 and Mn 2O 3 with 70% grade of Mn. After that a technical-economic assessment is carried out for a recycling plant with a feed capacity of 5000 t y -1 of only alkaline and zinc-carbon batteries. This analysis shows the economic feasibility of that plant, supposing a battery price surcharge of 0.5 € kg -1, with a return on investment of 34.5%, gross margin of 35.8% and around 3 years payback time.

  16. Electrode-active material for electrochemical batteries and method of preparation

    DOEpatents

    Varma, R.

    1983-11-07

    A battery electrode material comprises a non-stoichiometric electrode-active material which forms a redox pair with the battery electrolyte, an electrically conductive polymer present in the range of from about 2% by weight to about 5% by weight of the electrode-active material, and a binder. The conductive polymer provides improved proton or ion conductivity and is a ligand resulting in metal ion or negative ion vacancies of less than about 0.1 atom percent. Specific electrodes of nickel and lead are disclosed.

  17. Electrode-active material for electrochemical batteries and method of preparation

    DOEpatents

    Varma, Ravi

    1987-01-01

    A battery electrode material comprising a non-stoichiometric electrode-active material which forms a redox pair with the battery electrolyte, an electrically conductive polymer present in the range of from about 2% by weight to about 5% by weight of the electrode-active material, and a binder. The conductive polymer provides improved proton or ion conductivity and is a ligand resulting in metal ion or negative ion vacancies of less than about 0.1 atom percent. Specific electrodes of nickel and lead are disclosed.

  18. Method and apparatus for indicating electric charge remaining in batteries based on electrode weight and center of gravity

    DOEpatents

    Rouhani, S. Zia

    1996-01-01

    In most electrochemical batteries which generate electricity through the reaction of a battery electrode with an electrolyte solution, the chemical composition, and thus the weight and density, of the electrode changes as the battery discharges. The invention measures a parameter of the battery which changes as the weight of the electrode changes as the battery discharges and relates that parameter to the value of the parameter when the battery is fully charged and when the battery is functionally discharged to determine the state-of-charge of the battery at the time the parameter is measured. In one embodiment, the weight of a battery electrode or electrode unit is measured to determine the state-of-charge. In other embodiments, where a battery electrode is located away from the geometrical center of the battery, the position of the center of gravity of the battery or shift in the position of the center of gravity of the battery is measured (the position of the center of gravity changes with the change in weight of the electrode) and indicates the state-of-charge of the battery.

  19. Method and apparatus for indicating electric charge remaining in batteries based on electrode weight and center of gravity

    DOEpatents

    Rouhani, S.Z.

    1996-12-03

    In most electrochemical batteries which generate electricity through the reaction of a battery electrode with an electrolyte solution, the chemical composition, and thus the weight and density, of the electrode changes as the battery discharges. The invention measures a parameter of the battery which changes as the weight of the electrode changes as the battery discharges and relates that parameter to the value of the parameter when the battery is fully charged and when the battery is functionally discharged to determine the state-of-charge of the battery at the time the parameter is measured. In one embodiment, the weight of a battery electrode or electrode unit is measured to determine the state-of-charge. In other embodiments, where a battery electrode is located away from the geometrical center of the battery, the position of the center of gravity of the battery or shift in the position of the center of gravity of the battery is measured (the position of the center of gravity changes with the change in weight of the electrode) and indicates the state-of-charge of the battery. 35 figs.

  20. Simultaneous recovery of zinc and manganese dioxide from household alkaline batteries through hydrometallurgical processing

    NASA Astrophysics Data System (ADS)

    de Souza, Cleusa Cristina Bueno Martha; Tenório, Jorge Alberto Soares

    This paper describes the leaching experiments and the electrowinning tests to recover Zn and Mn from spent household alkaline batteries. After the dismantling of the batteries, the black powder was analyzed and found to contain 21 wt.% Zn and 45%wt. Mn. Therefore, it was considered that recovery of these metals would be interesting due to their relatively large amounts in this kind of waste. Batch laboratory experiments were carried out to develop an acid leaching procedure and to determine appropriate leaching conditions to maximize zinc extraction and to study the leaching behavior of Mn. An experimental study was undertaken to evaluate the feasibility of simultaneous recovery of zinc and particulate manganese dioxide using a laboratory cell. The results from these electrowinning experiments are also presented in this paper.

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

    NASA Astrophysics Data System (ADS)

    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.

  2. Highly Oriented Carbon Nanotube Sheets for Rechargeable Lithium Oxygen Battery Electrodes.

    PubMed

    Ryu, Seongwoo; Kim, Byung Gon; Choi, Jang Wook; Lee, Haeshin

    2015-10-01

    Lithium oxygen batteries are one of the next generation rechargeable batteries. High energy density of lithium oxygen batteries have been considered as a very attractive power option for electric vehicles and many other electronic devices. However, they still faced substantial challenges such as short cycle life, large voltage hysteresis, low gravimetric and volumetric power. Here we developed a highly aligned CNT structured sheet for favorable lithium oxygen cathode electrodes. We fabricated highly oriented CNT sheets by rolling vertically aligned CNT arrays. Highly oriented CNT sheets provide excellent electrical conductivity with favorable mesoporous structure for cathode electrode. As a result, the CNT sheet performed maximum discharging capacity of 1810 mA/gc. We found that electrical conductivity and pore distribution plays important rolls for improving performance in lithium oxygen batteries. This study suggests new strategies of designing highly efficient porous carbon electrodes for lithium oxygen batteries. PMID:26726383

  3. Tin nanoparticle thin film electrodes fabricated by the vacuum filtration method for enhanced battery performance.

    PubMed

    Lee, Jae Hyun; Kong, Byung-Seon; Baek, Youn-Kyoung; Yang, Seung Bo; Jung, Hee-Tae

    2009-06-10

    A novel method for fabricating tin nanoparticle thin film electrodes that show good performance in lithium ion batteries during cycling is reported. The vacuum filtration method has the advantage of affording a high degree of dispersion of the electrode components, thereby providing good electrical contacts between the tin nanoparticles and the conductive carbon or current collector. The reversible capacity and initial Coulombic efficiency are 726 mA h g(-1) and 85.3%, respectively, with this thin film electrode. Cycle life performance tests under real battery conditions show that the battery capacity and reaction peaks remained stable for up to 50 cycles. SEM shows that the uniform morphology of the vacuum filtered film was maintained throughout the cycle life test. This novel vacuum filtration method for providing nanoparticle-based film electrodes has further potential applications for use in various devices such as high power, thin film batteries, supercapacitors and organic-inorganic hybrid photovoltaic cells. PMID:19448286

  4. Thin film lithium-based batteries and electrochromic devices fabricated with nanocomposite electrode materials

    DOEpatents

    Gillaspie, Dane T; Lee, Se-Hee; Tracy, C. Edwin; Pitts, John Roland

    2014-02-04

    Thin-film lithium-based batteries and electrochromic devices (10) are fabricated with positive electrodes (12) comprising a nanocomposite material composed of lithiated metal oxide nanoparticles (40) dispersed in a matrix composed of lithium tungsten oxide.

  5. High performance binderless TiO2 nanowire arrays electrode for lithium-ion battery

    NASA Astrophysics Data System (ADS)

    Li, Yueming; Lv, Xiaojun; Li, Jinghong

    2009-09-01

    Binderless lithium ion battery electrode fabricated by anodizing Ti foil, in which TiO2 nanowire serves as active materials and unreacted Ti foil as the current collector, exhibited high electrochemical performance.

  6. Characterization of solid electrode materials using chronoamperometry: A study of the alkaline γ-MnO 2 electrode

    NASA Astrophysics Data System (ADS)

    Malloy, Aaron P.; Donne, Scott W.

    Large voltage step chronoamperometry is shown to be a time-efficient means to examine solid electrode materials compared with conventional electrochemical methods such as linear sweep voltammetry (LSV) and step potential electrochemical spectroscopy (SPECS), all the while providing comparable information concerning the rate capability of a material and its capacity. The applicability of the technique is demonstrated through a study of the alkaline γ-MnO 2 electrode. By sampling the current (and hence the charge) at various times after the chronoamperometric voltage step, the compatibility between chronoamperometry and LSV is disclosed. Furthermore, modelling of the chronoamperometric data using two curves based on a spherical diffusion model representing fast and slow discharge processes are found to be statistically suitable. From this modelling, values of A√ D (where A is the electrochemically active surface area and D is the diffusion coefficient) for the two processes are 3.89 × 10 -4 and 0.70 × 10 -4 cm 3 s -1/2 g -1, respectively, both of which are comparable with A√ D data extracted from a SPECS experiment on an identical electrode.

  7. Application of Carbon Nanomaterials in Lithium-Ion Battery Electrodes

    NASA Astrophysics Data System (ADS)

    Jaber-Ansari, Laila

    Carbon nanomaterials such as single-walled carbon nanotubes (SWCNTs) and graphene have emerged as leading additives for high capacity nanocomposite lithium ion battery electrodes due to their ability to improve electrode conductivity, current collection efficiency, and charge/discharge rate for high power applications. In this work, the these nanomaterials have been developed and their properties have been fine-tuned to help solve fundamental issues in conventional lithium ion battery electrodes. Towards this end, the application of SWCNTs in lithium-ion anodes has been studied. As-grown SWCNTs possess a distribution of physical and electronic structures, and it is of high interest to determine which subpopulations of SWCNTs possess the highest lithiation capacity and to develop processing methods that can enhance the lithiation capacity of underperforming SWCNT species. Towards this end, SWCNT electronic type purity is controlled via density gradient ultracentrifugation, enabling a systematic study of the lithiation of SWCNTs as a function of metal versus semiconducting content. Experimentally, vacuum filtered freestanding films of metallic SWCNTs are found to accommodate lithium with an order of magnitude higher capacity than their semiconducting counterparts. In contrast, SWCNT film densification leads to the enhancement of the lithiation capacity of semiconducting SWCNTs to levels comparable to metallic SWCNTs, which is corroborated by theoretical calculations. To understand the interaction of the graphene with lithium ions and electrolyte species during electrochemical we use Raman spectroscopy in a model system of monolayer graphene transferred on a Si(111) substrate and density functional theory (DFT) to investigate defect formation as a function of lithiation. This model system enables the early stages of defect formation to be probed in a manner previously not possible with commonly-used reduced graphene oxide or multilayer graphene substrates. Using ex

  8. Carbon nanotube/Co3O4 composite for air electrode of lithium-air battery

    NASA Astrophysics Data System (ADS)

    Yoon, Taek Han; Park, Yong Joon

    2012-01-01

    A carbon nanotube [CNT]/Co3O4 composite is introduced as a catalyst for the air electrode of lithium-air [Li/air] batteries. Co3O4 nanoparticles are successfully attached to the sidewall of the CNT by a hydrothermal method. A high discharge capacity and a low overvoltage indicate that the CNT/Co3O4 composite is a very promising catalyst for the air electrode of Li/air batteries.

  9. Carbon nanotube/Co3O4 composite for air electrode of lithium-air battery

    PubMed Central

    2012-01-01

    A carbon nanotube [CNT]/Co3O4 composite is introduced as a catalyst for the air electrode of lithium-air [Li/air] batteries. Co3O4 nanoparticles are successfully attached to the sidewall of the CNT by a hydrothermal method. A high discharge capacity and a low overvoltage indicate that the CNT/Co3O4 composite is a very promising catalyst for the air electrode of Li/air batteries. PMID:22222030

  10. Carbon nanotube/Co3O4 composite for air electrode of lithium-air battery.

    PubMed

    Yoon, Taek Han; Park, Yong Joon

    2012-01-01

    A carbon nanotube [CNT]/Co3O4 composite is introduced as a catalyst for the air electrode of lithium-air [Li/air] batteries. Co3O4 nanoparticles are successfully attached to the sidewall of the CNT by a hydrothermal method. A high discharge capacity and a low overvoltage indicate that the CNT/Co3O4 composite is a very promising catalyst for the air electrode of Li/air batteries. PMID:22222030

  11. Investigation of the Alkaline Electrochemical Interface and Development of Composite Metal/Metal-Oxides for Hydrogen and Oxygen Electrodes

    NASA Astrophysics Data System (ADS)

    Bates, Michael

    Understanding the fundamentals of electrochemical interfaces will undoubtedly reveal a path forward towards a society based on clean and renewable energy. In particular, it has been proposed that hydrogen can play a major role as an energy carrier of the future. To fully utilize the clean energy potential of a hydrogen economy, it is vital to produce hydrogen via water electrolysis, thus avoiding co-production of CO2 inherent to reformate hydrogen. While significant research efforts elsewhere are focused on photo-chemical hydrogen production from water, the inherent low efficiency of this method would require a massive land-use footprint to achieve sufficient hydrogen production rates to integrate hydrogen into energy markets. Thus, this research has primarily focused on the water splitting reactions on base-metal catalysts in the alkaline environment. Development of high-performance base-metal catalysts will help move alkaline water electrolysis to the forefront of hydrogen production methods, and when paired with solar and wind energy production, represents a clean and renewable energy economy. In addition to the water electrolysis reactions, research was conducted to understand the de-activation of reversible hydrogen electrodes in the corrosive environment of the hydrogen-bromine redox flow battery. Redox flow batteries represent a promising energy storage option to overcome the intermittency challenge of wind and solar energy production methods. Optimization of modular and scalable energy storage technology will allow higher penetration of renewable wind and solar energy into the grid. In Chapter 1, an overview of renewable energy production methods and energy storage options is presented. In addition, the fundamentals of electrochemical analysis and physical characterization of the catalysts are discussed. Chapter 2 reports the development of a Ni-Cr/C electrocatalyst with unprecedented mass-activity for the hydrogen evolution reaction (HER) in alkaline

  12. Polymer nanofiber-guided uniform lithium deposition for battery electrodes.

    PubMed

    Liang, Zheng; Zheng, Guangyuan; Liu, Chong; Liu, Nian; Li, Weiyang; Yan, Kai; Yao, Hongbin; Hsu, Po-Chun; Chu, Steven; Cui, Yi

    2015-05-13

    Lithium metal is one of the most promising candidates as an anode material for next-generation energy storage systems due to its highest specific capacity (3860 mAh/g) and lowest redox potential of all. The uncontrolled lithium dendrite growth that causes a poor cycling performance and serious safety hazards, however, presents a significant challenge for the realization of lithium metal-based batteries. Here, we demonstrate a novel electrode design by placing a three-dimensional (3D) oxidized polyacrylonitrile nanofiber network on top of the current collector. The polymer fiber with polar surface functional groups could guide the lithium ions to form uniform lithium metal deposits confined on the polymer fiber surface and in the 3D polymer layer. We showed stable cycling of lithium metal anode with an average Coulombic efficiency of 97.4% over 120 cycles in ether-based electrolyte at a current density of 3 mA/cm(2) for a total of 1 mAh/cm(2) of lithium. PMID:25822282

  13. Sulfonated polyaniline, a conducting polymer electrode for ion transfer batteries

    SciTech Connect

    Barbero, C.; Miras, M.C.; Koetz, R.; Haas, O.

    1994-12-31

    Sulfonated polyaniline (SPAN) was synthesized by sulfonation of polyaniline base with f6ming sulfuric acid. The polymer films were characterized by XPS, FFIR and UV-vis-NIR. XPS in combination with FTIR shows that the preparation procedure leads to a ca. 47% sulfonation of an otherwise unchanged polyaniline backbone. Electrodes modified with SPAN films exhibited two redox steps in aqueous as well as in nonaqueous electrolytes. Probe Beam Deflection and Quartz Crystal Microbalance were used to study the ion exchange mechanism. Protons are predominantly expelled during the first and second oxidation steps in acidic aqueous solution, accompanied by a counterflux of solvent. In nonaqueous electrolyte, expulsion of cations seems to be the dominant flux during SPAN oxidation, while solvent counterflux plays a significant role. The specific charge of SPAN films was found to be ca. 37 Ah/kg in aqueous solution (only first redox process used) and ca. 68 Ah/kg in nonaqueous media (both redox processes). Based on their experimental results, an estimation for a practical SPAN/Li battery would have 50% more specific energy than a PANI/Li one.

  14. Nitrogen-doped carbonaceous catalysts for gas-diffusion cathodes for alkaline aluminum-air batteries

    NASA Astrophysics Data System (ADS)

    Davydova, E. S.; Atamanyuk, I. N.; Ilyukhin, A. S.; Shkolnikov, E. I.; Zhuk, A. Z.

    2016-02-01

    Cobalt tetramethoxyphenyl porphyrin and polyacrylonitrile - based catalysts for oxygen reduction reaction were synthesized and characterized by means of SEM, TEM, XPS, BET, limited evaporation method, rotating disc and rotating ring-disc electrode methods. Half-cell and Al-air cell tests were carried out to determine the characteristics of gas-diffusion cathodes. Effect of active layer thickness and its composition on the characteristics of the gas-diffusion cathodes was investigated. Power density of 300 mW cm-2 was achieved for alkaline Al-air cell with an air-breathing polyacrylonitrile-based cathode.

  15. Effect of the length and surface area on electrochemical performance of cobalt oxide nanowires for alkaline secondary battery application

    NASA Astrophysics Data System (ADS)

    Xu, Yanan; Wang, Xiaofeng; An, Cuihua; Wang, Yijing; Jiao, Lifang; Yuan, Huatang

    2014-12-01

    One-dimensional porous Co3O4 nanowires with different length have been successfully synthesized by thermal decomposition of Co-NA polymer precursors at various hydrothermal reaction times. The positive effects of longer nanowires and larger surface area on electrochemical performance of Co3O4 samples were investigated systematically. All the as-prepared Co3O4 samples display excellent discharge capacities and cycle stability on account of large surface area and porous structure, indicating great potential application of porous Co3O4 nanowires for alkaline rechargeable batteries. The Co3O4-24 h sample with the longest length shows the most outstanding electrochemical performance, and displays the maximum discharge capacity of 450.1 mAh g-1 with the capacity retention of 90.4% after 100 cycles at a current density of 100 mA g-1. Electrochemical reactions between Co and Co(OH)2 occurring on the Co3O4 electrodes are investigated by XRD, cyclic voltammetry (CV) and charge-discharge measurements.

  16. Optimized Silicon Electrode Architecture, Interface, and Microgeometry for Next-Generation Lithium-Ion Batteries.

    PubMed

    Molina Piper, Daniela; Evans, Tyler; Xu, Shanshan; Kim, Seul Cham; Han, Sang Sub; Liu, Ken Liang; Oh, Kyu Hwan; Yang, Ronggui; Lee, Se-Hee

    2016-01-01

    Optimized performance of silicon-ionic- liquid lithium-ion batteries through the implementation of a new electrode-microgeometry. The incorporation of 1D silicon nanowires into the cyclized-polyacrylonitrile-based electrode-architecture allows for greatly improved active material utilization, higher rate capabilities, and reduced interfacial reactions. PMID:26506084

  17. Si composite electrode with Li metal doping for advanced lithium-ion battery

    SciTech Connect

    Liu, Gao; Xun, Shidi; Battaglia, Vincent

    2015-12-15

    A silicon electrode is described, formed by combining silicon powder, a conductive binder, and SLMP.TM. powder from FMC Corporation to make a hybrid electrode system, useful in lithium-ion batteries. In one embodiment the binder is a conductive polymer such as described in PCT Published Application WO 2010/135248 A1.

  18. Corrosion and anodic behaviour of zinc and its ternary alloys in alkaline battery electrolytes

    NASA Astrophysics Data System (ADS)

    Suresh Kannan, A. R.; Muralidharan, S.; Sarangapani, K. B.; Balaramachandran, V.; Kapali, V.

    Several attempts are being made to avoid the use of mercury-bearing zinc/zinc alloys as anodes in alkaline power sources. The work presented here suggests the possible use of some ternary alloys based on zinc of purity 99.9 to 99.95 wt.% as anodes in 10 M NaOH solution with sodium citrate, sodium stannate and calcium oxide as complexing agents and inhibitors. The corrosion of zinc and its alloys in 10 M NaOH solution is under cathodic control; in other alkaline electrolytes, it is under anodic control. Anode efficiency of up to 99.0% is achieved. The corrosion rates of zinc and its alloys are found to be comparable with those of mercury-bearing zinc in the chosen electrolytes. It is concluded that both dry cells and Zn-air batteries can be constructed with the above anodes and alkaline electrolytes. Thus, the presence of mercury, either in the anode or in the electrolyte, is avoided.

  19. R&D on lithium batteries in the USA: high-energy electrode materials

    NASA Astrophysics Data System (ADS)

    Owens, Boone B.; Smyrl, William H.; Xu, Jun John

    Recent trends in R&D on lithium battery technology in the USA continue to focus on high-performance batteries, polymer electrolyte systems and the development and production of batteries for specialty markets. Research on sol-gel derived amorphous vanadium and manganese oxides as high capacity, high-energy electrode materials has shown these morphologies are capable of reversibly intercalating very large amounts of lithium and they are attractive cathode candidates. Methods to improve the kinetics of these positive electrodes are showing promise.

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

    DOEpatents

    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.

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

    PubMed

    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. PMID:27189079

  2. Electrochemical investigation of polyhalide ion oxidation-reduction on carbon nanotube electrodes for redox flow batteries

    SciTech Connect

    Shao, Yuyan; Engelhard, Mark H.; Lin, Yuehe

    2009-10-01

    Polyhalide ions (Br-/BrCl2-) are an important redox couple for redox flow batteries. The oxidation-reduction behavior of polyhalide ions on a carbon nanotube (CNT) electrode has been investigated with cyclic voltammetry and electrochemical impedance spectroscopy. The onset oxidation potential of Br-/BrCl2- is negatively shifted by >100 mV, and the redox current peaks are greatly enhanced on a CNT electrode compared with that on the most widely-used graphite electrode. The reaction resistance of the redox couple (Br-/BrCl2-) is decreased on a CNT electrode. The redox reversibility is increased on a CNT electrode even though it still needs further improvement. CNT is a promising electrode material for redox flow batteries.

  3. Distribution of current in the electrodes of lead-acid batteries: a thermographic analysis approach

    NASA Astrophysics Data System (ADS)

    Streza, M.; Nuţ, C.; Tudoran, C.; Bunea, V.; Calborean, A.; Morari, C.

    2016-02-01

    An experimental method for the investigation of the current distribution in the electrodes of lead-acid batteries has been developed. The information is extracted by analysing the heat dissipation in the electrode during the discharge by using a high-performance IR camera. The effect of the current in the metallic grid can be de-convoluted from the total heat produced in the electrode by numerical processing of the temperature distribution over the electrode surface. By its simplicity and effectiveness, the proposed method has the potential to become an important tool in optimising electrode geometry.

  4. Nanostructured electrode materials for Li-ion battery

    NASA Astrophysics Data System (ADS)

    Balaya, Palani; Saravanan, Kuppan; Hariharan, Srirama

    2010-04-01

    Nanostructured materials have triggered a great excitement in recent times due to both fundamental interest as well as technological impact relevant for lithium ion batteries (LIBs). Size reduction in nanocrystals leads to a variety of unexpected exciting phenomena due to enhanced surface-to-volume ratio and reduced transport length. We will consider a few examples of nanostructured electrode materials in the context of lithium batteries for achieving high storage and high rate performances: 1) LiFePO4 nanoplates synthesized using solvothermal method could store Li-ions comparable to its theoretical capacity at C/10, while at 30C, they exhibit storage capacity up to 45 mAh/g. Size reduction (~30 nm) at the b-axis favors the fast Li-ion diffusion. In addition to this, uniform ~5 nm carbon coating throughout the plates provides excellent electronically conducting path for electrons. This nano architecture enables fast insertion/extraction of both Li-ions as well as electrons; 2) Mesporous-TiO2 with high surface area (135m2/g) synthesized using soft-template method exhibits high volumetric density compared to commercial nanopowder (P25), with excellent Li-storage behavior. C16 meso-TiO2 synthesized from CTAB exhibits reversible storage capacity of 288mAh/g at 0.2C and 109 mAh/g at 30C; 3) Zero strain Li4Ti5O12 anode material has been synthesized using several wet chemical routes. The best condition has been optimized to achieve storage capability close to theoretical limit of 175mAh/g at C/10. At 10C, we could retain lithium storage up to 88 mAh/g; 4) We report our recent results on α-Fe2O3 and γ-Fe2O3 using conversion reaction, providing insight for a better storage capability in γ-phase than the α-phase at 2C resulting solely from the nanocrystallinity.

  5. Method of Making a Nickel Fiber Electrode for a Nickel Based Battery System

    NASA Technical Reports Server (NTRS)

    Britton, Doris L. (Inventor)

    2001-01-01

    The general purpose of the invention is to develop a high specific energy nickel electrode for a nickel based battery system. The invention discloses a method of producing a lightweight nickel electrode which can be cycled to deep depths of discharge (i.e., 40% or greater of electrode capacity). These deep depths of discharge can be accomplished by depositing the required amount of nickel hydroxide active material into a lightweight nickel fiber substrate.

  6. In situ preparation of 1D Co@C composite nanorods as negative materials for alkaline secondary batteries.

    PubMed

    An, Cuihua; Wang, Yijing; Xu, Yanan; Wang, Ying; Huang, Yanan; Jiao, Lifang; Yuan, Huatang

    2014-03-26

    Cobalt-based coordination compounds were successfully prepared via employing nitrilotriacetic acid (NTA) as a complexing agent through a mild surfactant-free solvothermal process. Cobalt ions are linked with the amino group or carboxyl groups of NTA to become one-dimensional nanorods that can be proved by Fourier transform infrared measurement findings. The morphologies of the precursor Co-NTA highly depend on the solvent composition, the reaction time and temperature. The probable growth mechanism has been proposed. After heat treatment, the Co-NTA precursor can be completely converted into Co@C nanorods assembled by numerous core-shell-like Co@C nanoparticles, which preserved the rodlike morphology. The as-prepared Co@C composites display a rodlike morphology with 4 μm length and 100 nm diameter. The electrochemical performances of this novel Co@C material as the alkaline secondary Ni/Co battery negative electrode have been systematically researched. The discharge capacity of the Co@C-1 composite electrode can attain 609 mAh g(-1) and retains about 383.3 mAh g(-1) after 120 cycles (the discharge current density of 500 mA g(-1)). The novel material exhibits a high discharge capacity of 610 and 470 mAh g(-1) at discharge currents of 100 and 1000 mA g(-1), respectively. This suggests that approximately 77% of the discharge capacity is kept when the discharge current density is increased to 1000 mA g(-1) (10 times the initial current density of 100 mA g(-1)). The excellent electrochemical properties could be ascribed to the porous channels of the novel Co@C materials, which is beneficial to electrolyte diffusion and electrons and ions transportation. PMID:24571638

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

    SciTech Connect

    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

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

    NASA Astrophysics Data System (ADS)

    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.

  9. Layered perovskite oxide: a reversible air electrode for oxygen evolution/reduction in rechargeable metal-air batteries.

    PubMed

    Takeguchi, Tatsuya; Yamanaka, Toshiro; Takahashi, Hiroki; Watanabe, Hiroshi; Kuroki, Tomohiro; Nakanishi, Haruyuki; Orikasa, Yuki; Uchimoto, Yoshiharu; Takano, Hiroshi; Ohguri, Nobuaki; Matsuda, Motofumi; Murota, Tadatoshi; Uosaki, Kohei; Ueda, Wataru

    2013-07-31

    For the development of a rechargeable metal-air battery, which is expected to become one of the most widely used batteries in the future, slow kinetics of discharging and charging reactions at the air electrode, i.e., oxygen reduction reaction (ORR) and oxygen evolution reaction (OER), respectively, are the most critical problems. Here we report that Ruddlesden-Popper-type layered perovskite, RP-LaSr3Fe3O10 (n = 3), functions as a reversible air electrode catalyst for both ORR and OER at an equilibrium potential of 1.23 V with almost no overpotentials. The function of RP-LaSr3Fe3O10 as an ORR catalyst was confirmed by using an alkaline fuel cell composed of Pd/LaSr3Fe3O10-2x(OH)2x·H2O/RP-LaSr3Fe3O10 as an open circuit voltage (OCV) of 1.23 V was obtained. RP-LaSr3Fe3O10 also catalyzed OER at an equilibrium potential of 1.23 V with almost no overpotentials. Reversible ORR and OER are achieved because of the easily removable oxygen present in RP-LaSr3Fe3O10. Thus, RP-LaSr3Fe3O10 minimizes efficiency losses caused by reactions during charging and discharging at the air electrode and can be considered to be the ORR/OER electrocatalyst for rechargeable metal-air batteries. PMID:23802735

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

    DOEpatents

    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.

  11. Electrode-active material for electrochemical batteries and method of preparation

    SciTech Connect

    Varma, R.

    1987-08-18

    A method is described of preparing a battery electrode comprising providing an electrode-active material selected from chalogen-containing compounds of Ni, Fe, Pb, Co, Cu and mixtures thereof for a positive electrode and selected from the group consisting of Li, Na, K, Ca, Mg, Mn, Zn, Cd, Cu, Si, Al, Pb and alloys thereof for the negative electrode, mixing a ligand in the form of an electrically conductive polymer with the electrode-active material wherein the polymer is present in the range of from about 2% by weight to about 5% by weight of the electrode-active material, to provide metal ion or negative ion vacancies in the range of from about 0.05 to about 0.1 atom percent, the ligands for a positive electrode being selected from the class consisting of polyacetylene polymers having molecular weights in excess of 10,000 and cyclic polyamide with 3-5 functional groups. The ligands for a negative electrode are selected from the class consisting of tertiary butyl cyclohexyl-15-crown-5, TTF-TCNQ, and polymers of polyethylene oxide and one or more of LiCF/sub 3/SO/sub 3/, LiBr, Na/sub 2/S, and NaCN, mixing a binder with the electrode-active material and polymer, and forming the mixed electrode-active material and polymer and binder into a battery electrode.

  12. Silver-silver sulfate reference electrodes for use in lead-acid batteries

    NASA Astrophysics Data System (ADS)

    Ruetschi, Paul

    Electrochemical properties of silver-silver sulfate reference electrodes for lead-acid batteries are described, and the following possible applications discussed: Determination of individual capacities of positive and negative plates. Monitoring individual electrode behavior during deep discharge and cell reversal. Optimization charge or discharge parameters, by controlling the current such that pre-determined limits of positive or negative half-cell potential are respected. Observation of acid concentration differences, for example due to acid stratification, by measuring diffusion potentials (concentration-cell voltages). Detection of defective cells, and defective plate sets, in a string of cells, at the end of their service life. Silver-silver sulfate reference electrodes, permanently installed in lead-acid cells, may be a means to improve battery management, and therewith to improve reliability and service life. In vented batteries, reference electrodes may be used to limit positive plate polarization during charge, or float-charge. Limiting the positive half-cell potential to an upper, pre-set value would permit to keep anodic corrosion as low as possible. During cycling, discharge could be terminated when the half-cell potential of the positive electrode has dropped to a pre-set limit. This would prevent excessive discharge of the positive electrodes, which could result in an improvement of cycle life. In valve-regulated batteries, reference electrodes may be used to adjust float-charge conditions such as to assure sufficient cathodic polarization of the negative electrodes, in order to avoid sulfation. The use of such reference electrodes could be beneficial particularly in multi-cell batteries, with overall voltages above 12 V, operated in a partial-state-of-charge.

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

    DOEpatents

    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.

  14. Organo-sulfur molecules enable iron-based battery electrodes to meet the challenges of large-scale electrical energy storage

    SciTech Connect

    Yang, B; Malkhandi, S; Manohar, AK; Prakash, GKS; Narayanan, SR

    2014-07-03

    Rechargeable iron-air and nickel-iron batteries are attractive as sustainable and inexpensive solutions for large-scale electrical energy storage because of the global abundance and eco-friendliness of iron, and the robustness of iron-based batteries to extended cycling. Despite these advantages, the commercial use of iron-based batteries has been limited by their low charging efficiency. This limitation arises from the iron electrodes evolving hydrogen extensively during charging. The total suppression of hydrogen evolution has been a significant challenge. We have found that organo-sulfur compounds with various structural motifs (linear and cyclic thiols, dithiols, thioethers and aromatic thiols) when added in milli-molar concentration to the aqueous alkaline electrolyte, reduce the hydrogen evolution rate by 90%. These organo-sulfur compounds form strongly adsorbed layers on the iron electrode and block the electrochemical process of hydrogen evolution. The charge-transfer resistance and double-layer capacitance of the iron/electrolyte interface confirm that the extent of suppression of hydrogen evolution depends on the degree of surface coverage and the molecular structure of the organo-sulfur compound. An unanticipated electrochemical effect of the adsorption of organo-sulfur molecules is "de-passivation" that allows the iron electrode to be discharged at high current values. The strongly adsorbed organo-sulfur compounds were also found to resist electro-oxidation even at the positive electrode potentials at which oxygen evolution can occur. Through testing on practical rechargeable battery electrodes we have verified the substantial improvements to the efficiency during charging and the increased capability to discharge at high rates. We expect these performance advances to enable the design of efficient, inexpensive and eco-friendly iron-based batteries for large-scale electrical energy storage.

  15. Nickel hydroxide deposited indium tin oxide electrodes as electrocatalysts for direct oxidation of carbohydrates in alkaline medium

    NASA Astrophysics Data System (ADS)

    Ganesh, V.; Farzana, S.; Berchmans, Sheela

    In this work, the direct electrochemical oxidation of carbohydrates using nickel hydroxide modified indium tin oxide (ITO) electrodes in alkaline medium is demonstrated; suggesting the feasibility of using carbohydrates as a novel fuel in alkaline fuel cells applications. The chosen monosaccharides are namely glucose and fructose; disaccharides such as sucrose and lactose; and sugar acid like ascorbic acid for this study. ITO electrodes are chemically modified using a hexagonal lyotropic liquid crystalline phase template electrodeposition of nickel. Structural morphology, growth, orientation and electrochemical behaviour of Ni deposits are characterized using SEM, XRD, XPS and cyclic voltammetry (CV), respectively. Further electrochemical potential cycling process in alkaline medium is employed to convert these Ni deposits into corresponding nickel hydroxide modified electrodes. These electrodes are used as novel platform to perform the electrocatalytic oxidation of various carbohydrates in alkaline medium. It was found that bare and Ni coated ITO electrodes are inactive towards carbohydrates oxidation. The heterogeneous rate constant values are determined and calculated to be two orders of magnitude higher in the case of template method when compared to non-template technique. The observed effect is attributed to the synergistic effect of higher surface area of these deposits and catalytic ability of Ni(II)/Ni(III) redox couple.

  16. High energy density micro-fiber based nickel electrode for aerospace batteries

    NASA Technical Reports Server (NTRS)

    Francisco, Jennifer; Chiappetti, Dennis; Coates, Dwaine

    1996-01-01

    The nickel electrode is the specific energy limiting component in battery systems such as nickel-hydrogen, nickel-metal hydride and nickel-zinc. Lightweight, high energy density nickel electrodes have been developed which deliver in excess of 180 mAh/g at the one-hour discharge rate. These electrodes are based on a highly porous, nickel micro-fiber (less than 10 micron diameter) substrate, electrochemically impregnated with nickel-hydroxide active material. Electrodes are being tested both as a flooded half-cell and in full nickel-hydrogen and nickel-metal hydride cells. The electrode technology developed is applicable to commercial nickel-based batteries for applications such as electric vehicles, cellular telephones and laptop computers and for low-cost, high energy density military and aerospace applications.

  17. High energy density micro-fiber based nickel electrode for aerospace batteries

    SciTech Connect

    Francisco, J.; Chiappetti, D.; Coates, D.

    1996-11-01

    The nickel electrode is the specific energy limiting component in battery systems such as nickel-hydrogen, nickel-metal hydride and nickel-zinc. Lightweight, high energy density nickel electrodes have been developed which deliver in excess of 180 mAh/g at the one-hour discharge rate. These electrodes are based on a highly porous, nickel micro-fiber (< 10 micron diameter) substrate, electrochemically impregnated with nickel-hydroxide active material. Electrodes are being tested both as a flooded half-cell and in full nickel-hydrogen and nickel-metal hydride cells. The electrode technology developed is applicable to commercial nickel-based batteries for applications such as electric vehicles, cellular telephones and laptop computers and for low-cost, high energy density military and aerospace applications.

  18. High energy density micro-fiber based nickel electrode for aerospace batteries

    SciTech Connect

    Francisco, J.; Chiappetti, D.; Coates, D.

    1996-02-01

    The nickel electrode is the specific energy limiting component in battery systems such as nickel-hydrogen, nickel-metal hydride and nickel-zinc. Lightweight, high energy density nickel electrodes have been developed which deliver in excess of 180 mAh/g at the one-hour discharge rate. These electrodes are based on a highly porous, nickel micro-fiber (less than 10 micron diameter) substrate, electrochemically impregnated with nickel-hydroxide active material. Electrodes are being tested both as a flooded half-cell and in full nickel-hydrogen and nickel-metal hydride cells. The electrode technology developed is applicable to commercial nickel-based batteries for applications such as electric vehicles, cellular telephones and laptop computers and for low-cost, high energy density military and aerospace applications.

  19. Formation of Nanocrystalline Surface of Cu-Sn Alloy Foam Electrochemically Produced for Li-Ion Battery Electrode.

    PubMed

    Ye, Bora; Kim, Sunjung

    2015-10-01

    Cu-Sn alloy foam is a promising electrode material for Li-ion batteries. In this study, Cu-Sn alloy foam was produced by diffusion-limited electrodeposition in alkaline electrolyte using polyurethane (PU) foam template. Our major concern is to form Cu-Sn alloy foam with nanocrystalline surface morphology by adjusting electrodeposition conditions such as deposition potential and metal ion concentration. Cu-Sn alloy layers comprising of nanoclusters such as nanospheres, nanoellipsoids, and nanoflakes were created depending on electrodeposition conditions. Larger surface area of nanocluster-interconnected Cu-Sn alloy layer was created when both Sn concentration and negative deposition potential were higher. After decomposing PU template thermally, Cu-Sn alloy foam of Cu, Cu6Sn5, and Cu3Sn phases was finally produced. PMID:26726491

  20. Electrodeposition of preferentially oriented zinc for flow-assisted alkaline batteries

    SciTech Connect

    Desai, D; Wei, X; Steingart, DA; Banerjee, S

    2014-06-15

    Preferred orientation of zinc deposits during charging is shown to significantly improve performance and cycle life in flow-assisted alkaline zinc batteries, which has not been demonstrated earlier. The preferred orientation of zinc deposits was investigated using X-ray diffraction (XRD). Compact zinc is found to have (11 (2) over bar2) preferred orientation on brass, which contributes to similar to 60% of the texture. The effect of charging current and zincate concentration on morphology was investigated in a rotating hull cell and correlated with anodic efficiency. Compact zinc deposits are found to have a fine-grained, bright finish and the highest anodic efficiency. Electrochemical impedance spectroscopy (EIS) proves that compact zinc corresponds to the minimum in the half-cell resistance. Morphological control using compact zinc could be accomplished using innovations such as pulse charging or enhanced mass-transfer to improve anode performance without affecting the cathode. (C) 2014 Elsevier B.V. All rights reserved.

  1. Electrodeposition of preferentially oriented zinc for flow-assisted alkaline batteries

    NASA Astrophysics Data System (ADS)

    Desai, Divyaraj; Wei, Xia; Steingart, Daniel A.; Banerjee, Sanjoy

    2014-06-01

    Preferred orientation of zinc deposits during charging is shown to significantly improve performance and cycle life in flow-assisted alkaline zinc batteries, which has not been demonstrated earlier. The preferred orientation of zinc deposits was investigated using X-ray diffraction (XRD). Compact zinc is found to have (11 2 bar 2) preferred orientation on brass, which contributes to ∼60% of the texture. The effect of charging current and zincate concentration on morphology was investigated in a rotating hull cell and correlated with anodic efficiency. Compact zinc deposits are found to have a fine-grained, bright finish and the highest anodic efficiency. Electrochemical impedance spectroscopy (EIS) proves that compact zinc corresponds to the minimum in the half-cell resistance. Morphological control using compact zinc could be accomplished using innovations such as pulse charging or enhanced mass-transfer to improve anode performance without affecting the cathode.

  2. Recovery of zinc and manganese from alkaline and zinc-carbon spent batteries

    NASA Astrophysics Data System (ADS)

    De Michelis, I.; Ferella, F.; Karakaya, E.; Beolchini, F.; Vegliò, F.

    This paper concerns the recovery of zinc and manganese from alkaline and zinc-carbon spent batteries. The metals were dissolved by a reductive-acid leaching with sulphuric acid in the presence of oxalic acid as reductant. Leaching tests were realised according to a full factorial design, then simple regression equations for Mn, Zn and Fe extraction were determined from the experimental data as a function of pulp density, sulphuric acid concentration, temperature and oxalic acid concentration. The main effects and interactions were investigated by the analysis of variance (ANOVA). This analysis evidenced the best operating conditions of the reductive acid leaching: 70% of manganese and 100% of zinc were extracted after 5 h, at 80 °C with 20% of pulp density, 1.8 M sulphuric acid concentration and 59.4 g L -1 of oxalic acid. Both manganese and zinc extraction yields higher than 96% were obtained by using two sequential leaching steps.

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

    NASA Astrophysics Data System (ADS)

    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.

  4. Visualization of Charge Distribution in a Lithium Battery Electrode

    SciTech Connect

    Liu, Jun; Kunz, Martin; Chen, Kai; Tamura, Nobumichi; Richardson, Thomas J.

    2010-07-02

    We describe a method for direct determination and visualization of the distribution of charge in a composite electrode. Using synchrotron X-ray microdiffraction, state-of-charge profiles in-plane and normal to the current collector were measured. In electrodes charged at high rate, the signatures of nonuniform current distribution were evident. The portion of a prismatic cell electrode closest to the current collector tab had the highest state of charge due to electronic resistance in the composite electrode and supporting foil. In a coin cell electrode, the active material at the electrode surface was more fully charged than that close to the current collector because the limiting factor in this case is ion conduction in the electrolyte contained within the porous electrode.

  5. Expansion and shrinkage of the sulfur composite electrode in rechargeable lithium batteries

    NASA Astrophysics Data System (ADS)

    He, Xiangming; Ren, Jianguo; Wang, Li; Pu, Weihua; Jiang, Changyin; Wan, Chunrong

    The expansion and shrinkage characteristics of sulfur composite cathode electrode in rechargeable lithium batteries have been investigated. It was found that the sulfur composites electrodes expanded when discharging and shrank when charging again. The thickness change of the electrode was measured to be about 22%. The thickness of lithium metal anodes was also changed when lithium deposition and dissolution, while the sulfur composites electrodes expanded and shrank conversely. The investigation showed that the thickness changes of lithium anode and sulfur composite cathode could be compensated with each other to keep the total thickness of the cell not to change so much.

  6. Thermal treatment for recovery of manganese and zinc from zinc-carbon and alkaline spent batteries

    SciTech Connect

    Belardi, G.; Lavecchia, R.; Medici, F.; Piga, L.

    2012-10-15

    Highlights: Black-Right-Pointing-Pointer We separated Zn from Mn in zinc-carbon and alkaline batteries after removal of Hg. Black-Right-Pointing-Pointer Almost total removal of Hg is achieved at low temperature in air. Black-Right-Pointing-Pointer Nitrogen atmosphere is needed to reduce zinc and to permit its volatilization. Black-Right-Pointing-Pointer A high grade Zn concentrate was obtained with a high recovery at 1000-1200 Degree-Sign C. Black-Right-Pointing-Pointer The grade of Mn in the residue was enhanced with complete recovery. - Abstract: The aim of this paper is the recovery of manganese and zinc from a mixture of zinc-carbon and alkaline spent batteries, containing 40.9% of Mn and 30.1% of Zn, after preliminary physical treatment followed by removal of mercury. Separation of the metals has been carried out on the basis of their different boiling points, being 357 Degree-Sign C and 906 Degree-Sign C the boiling point of mercury and zinc and 1564 Degree-Sign C the melting point of Mn{sub 2}O{sub 3}. Characterization by chemical analysis, TGA/DTA and X-ray powder diffraction of the mixture has been carried out after comminution sieving and shaking table treatment to remove the anodic collectors and most of chlorides contained in the mixture. The mixture has been roasted at various temperatures and resident times in a flow of air to set the best conditions to remove mercury that were 400 Degree-Sign C and 10 min. After that, the flow of air has been turned into a nitrogen one (inert atmosphere) and the temperatures raised, thus permitting the zinc oxide to be reduced to metallic zinc by the carbon present in the original mixture and recovered after volatilization as a high grade concentrate, while manganese was left in the residue. The recovery and the grade of the two metals, at 1000 Degree-Sign C and 30 min residence time, were 84% and 100% for zinc and 85% and 63% for manganese, respectively. The recovery of zinc increased to 99% with a grade of 97% at

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

    NASA Astrophysics Data System (ADS)

    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.

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

    DOE PAGESBeta

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

    2016-02-21

    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. Additionally, 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 NMCmore » 532 electrodes. 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. In conclusion, 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.« less

  9. EXAFS studies of battery materials

    SciTech Connect

    McBreen, J.

    1991-12-31

    X-ray absorption spectroscopy (XAS) has been used at extensively at Brookhaven National Laboratory (BNL) to study materials and electrodes of several battery systems. The power and the general applicability of the technique is illustrated by studies of several battery materials such as PEO-salt complexes, PbO{sub 2}, and in situ studies of mossy zinc deposition in alkaline electrolyte.

  10. EXAFS studies of battery materials

    SciTech Connect

    McBreen, J.

    1991-01-01

    X-ray absorption spectroscopy (XAS) has been used at extensively at Brookhaven National Laboratory (BNL) to study materials and electrodes of several battery systems. The power and the general applicability of the technique is illustrated by studies of several battery materials such as PEO-salt complexes, PbO{sub 2}, and in situ studies of mossy zinc deposition in alkaline electrolyte.

  11. The cell-in-series method: A technique for accelerated electrode degradation in redox flow batteries

    SciTech Connect

    Pezeshki, Alan M.; Sacci, Robert L.; Veith, Gabriel M.; Zawodzinski, Thomas A.; Mench, Matthew M.

    2015-11-21

    Here, we demonstrate a novel method to accelerate electrode degradation in redox flow batteries and apply this method to the all-vanadium chemistry. Electrode performance degradation occurred seven times faster than in a typical cycling experiment, enabling rapid evaluation of materials. This method also enables the steady-state study of electrodes. In this manner, it is possible to delineate whether specific operating conditions induce performance degradation; we found that both aggressively charging and discharging result in performance loss. Post-mortem x-ray photoelectron spectroscopy of the degraded electrodes was used to resolve the effects of state of charge (SoC) and current on the electrode surface chemistry. For the electrode material tested in this work, we found evidence that a loss of oxygen content on the negative electrode cannot explain decreased cell performance. Furthermore, the effects of decreased electrode and membrane performance on capacity fade in a typical cycling battery were decoupled from crossover; electrode and membrane performance decay were responsible for a 22% fade in capacity, while crossover caused a 12% fade.

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

    PubMed

    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

    2016-04-01

    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. PMID:26833897

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

    PubMed

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

    2010-02-21

    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 Li(2)O(2) electrode and show that in the presence of Li vacancies Li(2)O(2) becomes a conductor. PMID:20170208

  14. Magnetically aligned graphite electrodes for high-rate performance Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Billaud, Juliette; Bouville, Florian; Magrini, Tommaso; Villevieille, Claire; Studart, André R.

    2016-08-01

    As lithium-ion batteries become ubiquitous, the energy storage market is striving for better performance, longer lifetime and better safety of the devices. This race for performance is often focused on the search for new materials, whereas less effort has been dedicated to the electrode engineering. Enhancing the power density by increasing the amount of active material remains impractical since it impinges the transport of ions across the electrode during the charging and discharging processes. Here, we show that the electrochemical performance of a battery containing a thick (about 200 μm), highly loaded (about 10 mg cm‑2) graphite electrode can be remarkably enhanced by fabricating anodes with an out-of-plane aligned architecture using a low external magnetic field. The lower tortuosity resulting from such a simple and scalable magnetic alignment approach leads to a specific charge up to three times higher than that of non-architectured electrodes at a rate of 1C.

  15. Laboratory-scale evaluation of secondary alkaline zinc batteries for electric vehicles

    NASA Astrophysics Data System (ADS)

    Striebel, Kathryn A.; McLarnon, Frank R.; Cairns, Elton J.

    Two types of secondary zinc cell have been evaluated in our laboratory to assess their suitability to power an electric van. Single cells were charged and discharged with constant-current cycles as well as with controlled-power discharge profiles, scaled to the predicted mass of a full-size battery. Both cells were able to meet the requirements for power discharge specified by the so-called Simplified Federal Urban Driving Schedule (SFUDS) early in life (the first 15 cycles). The Zn/air cell achieved an average of 72 SFUDS repetions (7.2 h) per discharge. The Zn/NiOOH cell achieved an average of 51 SFUDS repetitions (5.1 h) per discharge. The bifunctional air electrodes did not reach oxygen-evolution potentials during the 8-s regenerative breaking portions of the SFUDS cycle.

  16. Characterization of the products attained from a thermal treatment of a mix of zinc-carbon and alkaline batteries.

    PubMed

    Kuo, Yi-Ming; Lin, Chitsan; Wang, Jian-Wen; Huang, Kuo-Lin; Tsai, Cheng-Hsien; Wang, Chih-Ta

    2016-01-01

    This study applies a thermal separation process (TSP) to recover Fe, Mn, and Zn from hazardous spent zinc-carbon and alkaline batteries. In the TSP, the batteries were heated together with a reducing additive and the metals in batteries, according to their boiling points and densities, were found to move into three major output materials: slag, ingot (mainly Fe and Mn), and particulate (particularly Zn). The slag well encapsulated the heavy metals of interest and can be recycled for road pavement or building materials. The ingot had high levels of Fe (522,000 mg/kg) and Mn (253,000 mg/kg) and can serve as an additive for stainless steel-making processes. The particulate phase had a Zn level of 694,000 mg/kg which is high enough to be directly sold for refinement. Overall, the TSP effectively recovered valuable metals from the hazardous batteries. PMID:26582065

  17. Aquagel electrode separator for use in batteries and supercapacitors

    DOEpatents

    Mayer, S.T.; Kaschmitter, J.L.; Pekala, R.W.

    1995-03-28

    An electrode separator is described for electrochemical energy storage devices, such as a high energy density capacitor incorporating a variety of carbon foam electrodes. The separator is derived from an aquagel of resorcinol-formaldehyde and related polymers and containing ionically conducting electrolyte in the pores thereof. 9 figures.

  18. Aquagel electrode separator for use in batteries and supercapacitors

    DOEpatents

    Mayer, Steven T.; Kaschmitter, James L.; Pekala, Richard W.

    1995-01-01

    An electrode separator for electrochemical energy storage devices, such as a high energy density capacitor incorporating a variety of carbon foam electrodes. The separator is derived from an aquagel of resorcinol-formaldehyde and related polymers and containing ionically conducting electrolyte in the pores thereof.

  19. Oriented nanotube electrodes for lithium ion batteries and supercapacitors

    DOEpatents

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  1. Mapping spatially inhomogeneous electrochemical reactions in battery electrodes using high energy X-rays.

    PubMed

    Borkiewicz, Olaf J; Chapman, Karena W; Chupas, Peter J

    2013-06-14

    The spatial distribution of a reaction through a lithium-ion battery electrode has been resolved using micro-beam high-energy X-ray scattering measurements coupled with Pair Distribution Function (PDF) analysis. The electrochemical reaction was most advanced at the interface between the electrode and electrolyte-soaked separator, with linear variation in reaction progress with distance from this interface. PMID:23598687

  2. 3D Interconnected Electrode Materials with Ultrahigh Areal Sulfur Loading for Li-S Batteries.

    PubMed

    Fang, Ruopian; Zhao, Shiyong; Hou, Pengxiang; Cheng, Min; Wang, Shaogang; Cheng, Hui-Ming; Liu, Chang; Li, Feng

    2016-05-01

    Sulfur electrodes based on a 3D integrated hollow carbon fiber foam (HCFF) are synthesized with high sulfur loadings of 6.2-21.2 mg cm(-2) . Benefiting from the high electrolyte absorbability of the HCFF and the multiple conductive channels, the obtained electrode demonstrates excellent cycling stability and a high areal capacity of 23.32 mAh cm(-2) , showing great promise in commercially viable Li-S batteries. PMID:26932832

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

    PubMed

    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. PMID:27168478

  4. Dry cell battery poisoning

    MedlinePlus

    Batteries - dry cell ... Acidic dry cell batteries contain: Manganese dioxide Ammonium chloride Alkaline dry cell batteries contain: Sodium hydroxide Potassium hydroxide Lithium dioxide dry cell batteries ...

  5. The cell-in-series method: A technique for accelerated electrode degradation in redox flow batteries

    DOE PAGESBeta

    Pezeshki, Alan M.; Sacci, Robert L.; Veith, Gabriel M.; Zawodzinski, Thomas A.; Mench, Matthew M.

    2015-11-21

    Here, we demonstrate a novel method to accelerate electrode degradation in redox flow batteries and apply this method to the all-vanadium chemistry. Electrode performance degradation occurred seven times faster than in a typical cycling experiment, enabling rapid evaluation of materials. This method also enables the steady-state study of electrodes. In this manner, it is possible to delineate whether specific operating conditions induce performance degradation; we found that both aggressively charging and discharging result in performance loss. Post-mortem x-ray photoelectron spectroscopy of the degraded electrodes was used to resolve the effects of state of charge (SoC) and current on the electrodemore » surface chemistry. For the electrode material tested in this work, we found evidence that a loss of oxygen content on the negative electrode cannot explain decreased cell performance. Furthermore, the effects of decreased electrode and membrane performance on capacity fade in a typical cycling battery were decoupled from crossover; electrode and membrane performance decay were responsible for a 22% fade in capacity, while crossover caused a 12% fade.« less

  6. Durability of carbon-plastic electrodes for zinc/bromine storage batteries

    NASA Astrophysics Data System (ADS)

    Arnold, C., Jr.

    1992-10-01

    In previous work, failure of early versions of the zinc/bromine battery was traced to degradation and warpage of the carbon-plastic electrode. These electrodes were fabricated from copolymers of ethylene and propylene (EP) containing structures that were found to be susceptible to degradation by the electrolyte. In this work, we evaluated two developmental electrodes from Johnson Controls Battery Group, Inc., in which the EP copolymer was replaced with a high-density polyethylene (HDPE) that contained glass-fiber reinforcing fillers. The glass fiber content of these two electrodes was different (19 vs. 31 percent). We determined the effect of electrolyte on sorption behavior, dimensional stability, chemical stability, and thermal, mechanical, and electrical properties under real-time and accelerated aging conditions. We also characterized unaged samples of both electrodes to determine their chemical composition and physical structure. We found that high glass content in the electrode minimizes sorption and increases dimensional stability. Both high and low glass content electrodes were found to be chemically and thermally stable toward the electrolyte. A slight decrease in the storage modulus (G') of both electrodes was attributed to sorption of non-ionic and hydrophobic ingredients in the electrolyte. The electrical conductivity of both electrodes appeared to improve (increase) upon exposure to the electrolyte. No time or temperature trends were observed for the chemical, thermal, or mechanical properties of electrodes made from HDPE. Since decreases in these properties were noted for electrodes made from EP copolymers under similar conditions, it appears that the HDPE-based electrodes have superior long-term stability in the ZnBr2 environment.

  7. High-performance of PbO2 nanowire electrodes for lead-acid battery

    NASA Astrophysics Data System (ADS)

    Moncada, A.; Mistretta, M. C.; Randazzo, S.; Piazza, S.; Sunseri, C.; Inguanta, R.

    2014-06-01

    PbO2 nanowires were obtained by template electrodeposition in polycarbonate membranes and tested as positive electrode for lead-acid battery. Nanowires were grown on the same material acting as current collector that was electrodeposited too. The nanostructured electrodes were assembled in a zero-gap configuration using commercial negative plate and separator. Cell performance was tested by galvanostatic charge/discharge cycles in a 5 M H2SO4 aqueous electrolyte. PbO2 nanostructured electrodes were able to deliver at 1C rate an almost constant capacity of about 190 mAh g-1 (85% of active material utilization), close to the theoretical value (224 mAh g-1). The nanowire array provides a very large surface area (about 70 times higher than the geometrical one) that enhances the specific capacity of the battery. SEM images of the as-prepared and cycled electrodes showed that nanowires morphology changes significantly after the initial cycles. Change of morphology led to the formation of very spongy structure, characterized by the presence of macro-voids, which ensured penetration of the electrolyte in the inner areas of the electrode. Besides, PbO2 nanowires showed a very good cycling stability, maintained for more than 1000 cycles. These findings indicate that this new type of electrode might be a promising substitute of positive plates in lead-acid battery.

  8. Recovery of manganese oxides from spent alkaline and zinc–carbon batteries. An application as catalysts for VOCs elimination

    SciTech Connect

    Gallegos, María V.; Falco, Lorena R.; Peluso, Miguel A.; Sambeth, Jorge E.; Thomas, Horacio J.

    2013-06-15

    Highlights: • Manganese oxides were synthesized using spent batteries as raw materials. • Spent alkaline and zinc–carbon size AA batteries were used. • A biohydrometallurgical process was employed to bio-lixiviate batteries. • Manganese oxides were active in the oxidation of VOCs (ethanol and heptane). - Abstract: Manganese, in the form of oxide, was recovered from spent alkaline and zinc–carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO{sub 4} solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnO{sub x} synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn{sub 2}O{sub 3} in the EMO and the CMO samples, together with some Mn{sup 4+} cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn{sub 3}O{sub 4}. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200 °C, while heptane requires more than 400 °C. The CMO has the highest oxide selectivity to CO{sub 2}. The results show that manganese oxides obtained using spent alkaline and zinc–carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs.

  9. Applications of porous electrodes to metal-ion removal and the design of battery systems

    SciTech Connect

    Trost, G.G.

    1983-09-01

    This dissertation treats the use of porous electrodes as electrochemical reactors for the removal of dilute metal ions. A methodology for the scale-up of porous electrodes used in battery applications is given. Removal of 4 ..mu..g Pb/cc in 1 M sulfuric acid was investigated in atmospheric and high-pressure, flow-through porous reactors. The atmospheric reactor used a reticulated vitreous carbon porous bed coated in situ with a mercury film. Best results show 98% removal of lead from the feed stream. Results are summarized in a dimensionless plot of Sherwood number vs Peclet number. High-pressure, porous-electrode experiments were performed to investigate the effect of pressure on the current efficiency. Pressures were varied up to 120 bar on electrode beds of copper or lead-coated spheres. The copper spheres showed high hydrogen evolution rates which inhibited lead deposition, even at high cathodic overpotentials. Use of lead spheres inhibited hydrogen evolution but often resulted in the formation of lead sulfate layers; these layers were difficult to reduce back to lead. Experimental data of one-dimensional porous battery electrodes are combined with a model for the current collector and cell connectors to predict ultimate specific energy and maximum specific power for complete battery systems. Discharge behavior of the plate as a whole is first presented as a function of depth of discharge. These results are combined with the voltage and weight penalties of the interconnecting bus and post, positive and negative active material, cell container, etc. to give specific results for the lithium-aluminum/iron sulfide high-temperature battery. Subject to variation is the number of positive electrodes, grid conductivity, minimum current-collector weight, and total delivered capacity. The battery can be optimized for maximum energy or power, or a compromise design may be selected.

  10. Thermal treatment for recovery of manganese and zinc from zinc-carbon and alkaline spent batteries.

    PubMed

    Belardi, G; Lavecchia, R; Medici, F; Piga, L

    2012-10-01

    The aim of this paper is the recovery of manganese and zinc from a mixture of zinc-carbon and alkaline spent batteries, containing 40.9% of Mn and 30.1% of Zn, after preliminary physical treatment followed by removal of mercury. Separation of the metals has been carried out on the basis of their different boiling points, being 357°C and 906°C the boiling point of mercury and zinc and 1564°C the melting point of Mn(2)O(3). Characterization by chemical analysis, TGA/DTA and X-ray powder diffraction of the mixture has been carried out after comminution sieving and shaking table treatment to remove the anodic collectors and most of chlorides contained in the mixture. The mixture has been roasted at various temperatures and resident times in a flow of air to set the best conditions to remove mercury that were 400°C and 10 min. After that, the flow of air has been turned into a nitrogen one (inert atmosphere) and the temperatures raised, thus permitting the zinc oxide to be reduced to metallic zinc by the carbon present in the original mixture and recovered after volatilization as a high grade concentrate, while manganese was left in the residue. The recovery and the grade of the two metals, at 1000°C and 30 min residence time, were 84% and 100% for zinc and 85% and 63% for manganese, respectively. The recovery of zinc increased to 99% with a grade of 97% at 1200°C and 30 min residence time, while the recovery and grade of manganese were 86% and 87%, respectively, at that temperature. Moreover, the chlorinated compounds that could form by the combustion of the plastics contained in the spent batteries, are destroyed at the temperature required by the process. PMID:22677015

  11. Reactivity of carbon in lithium-oxygen battery positive electrodes.

    PubMed

    Itkis, Daniil M; Semenenko, Dmitry A; Kataev, Elmar Yu; Belova, Alina I; Neudachina, Vera S; Sirotina, Anna P; Hävecker, Michael; Teschner, Detre; Knop-Gericke, Axel; Dudin, Pavel; Barinov, Alexei; Goodilin, Eugene A; Shao-Horn, Yang; Yashina, Lada V

    2013-10-01

    Unfortunately, the practical applications of Li-O2 batteries are impeded by poor rechargeability. Here, for the first time we show that superoxide radicals generated at the cathode during discharge react with carbon that contains activated double bonds or aromatics to form epoxy groups and carbonates, which limits the rechargeability of Li-O2 cells. Carbon materials with a low amount of functional groups and defects demonstrate better stability thus keeping the carbon will-o'-the-wisp lit for lithium-air batteries. PMID:24004050

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

    SciTech Connect

    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.

  13. Electrode architectures for efficient electronic and ionic transport pathways in high power lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Faulkner, Ankita Shah

    As the demand for clean energy sources increases, large investments have supported R&D programs aimed at developing high power lithium ion batteries for electric vehicles, military, grid storage and space applications. State of the art lithium ion technology cannot meet power demands for these applications due to high internal resistances in the cell. These resistances are mainly comprised of ionic and electronic resistance in the electrode and electrolyte. Recently, much attention has been focused on the use of nanoscale lithium ion active materials on the premise that these materials shorten the diffusion length of lithium ions and increase the surface area for electrochemical charge transfer. While, nanomaterials have allowed significant improvements in the power density of the cell, they are not a complete solution for commercial batteries. Due to their large surface area, they introduce new challenges such as a poor electrode packing densities, high electrolyte reactivity, and expensive synthesis procedures. Since greater than 70% of the cost of the electric vehicle is due to the cost of the battery, a cost-efficient battery design is most critical. To address the limitations of nanomaterials, efficient transport pathways must be engineered in the bulk electrode. As a part of nanomanufacturing research being conducted the Center for High-rate Nanomanufacturing at Northeastern University, the first aim of the proposed work is to develop electrode architectures that enhance electronic and ionic transport pathways in large and small area lithium ion electrodes. These architectures will utilize the unique electronic and mechanical properties of carbon nanotubes to create robust electrode scaffolding that improves electrochemical charge transfer. Using extensive physical and electrochemical characterization, the second aim is to investigate the effect of electrode parameters on electrochemical performance and evaluate the performance against standard commercial

  14. Imidazolium-based Block Copolymers as Solid-State Separators for Alkaline Fuel Cells and Lithium Ion Batteries

    NASA Astrophysics Data System (ADS)

    Nykaza, Jacob Richard

    In this study, polymerized ionic liquid (PIL) diblock copolymers were explored as solid-state polymer separators as an anion exchange membrane (AEM) for alkaline fuel cells AFCs and as a solid polymer electrolyte (SPE) for lithium-ion batteries. Polymerized ionic liquid (PIL) block copolymers are a distinct set of block copolymers that combine the properties of both ionic liquids (e.g., high conductivity, high electrochemical stability) and block copolymers (e.g., self-assembly into various nanostructures), which provides the opportunity to design highly conductive robust solid-state electrolytes that can be tuned for various applications including AFCs and lithium-ion batteries via simple anion exchange. A series of bromide conducting PIL diblock copolymers with an undecyl alkyl side chain between the polymer backbone and the imidazolium moiety were first synthesized at various compositions comprising of a PIL component and a non-ionic component. Synthesis was achieved by post-functionalization from its non-ionic precursor PIL diblock copolymer, which was synthesized via the reverse addition fragmentation chain transfer (RAFT) technique. This PIL diblock copolymer with long alkyl side chains resulted in flexible, transparent films with high mechanical strength and high bromide ion conductivity. The conductivity of the PIL diblock copolymer was three times higher than its analogous PIL homopolymer and an order of magnitude higher than a similar PIL diblock copolymer with shorter alkyl side chain length, which was due to the microphase separated morphology, more specifically, water/ion clusters within the PIL microdomains in the hydrated state. Due to the high conductivity and mechanical robustness of this novel PIL block copolymer, its application as both the ionomer and AEM in an AFC was investigated via anion exchange to hydroxide (OH-), where a maximum power density of 29.3 mW cm-1 (60 °C with H2/O2 at 25 psig (172 kPa) backpressure) was achieved. Rotating disk

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

    SciTech Connect

    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.

  16. New layered metal oxides as positive electrode materials for room-temperature sodium-ion batteries

    NASA Astrophysics Data System (ADS)

    Mu, Lin-Qin; Hu, Yong-Sheng; Chen, Li-Quan

    2015-03-01

    In order to achieve better Na storage performance, most layered oxide positive electrode materials contain toxic and expensive transition metals Ni and/or Co, which are also widely used for lithium-ion batteries. Here we report a new quaternary layered oxide consisting of Cu, Fe, Mn, and Ti transition metals with O3-type oxygen stacking as a positive electrode for room-temperature sodium-ion batteries. The material can be simply prepared by a high-temperature solid-state reaction route and delivers a reversible capacity of 94 mAh/g with an average storage voltage of 3.2 V. This paves the way for cheaper and non-toxic batteries with high Na storage performance. Project supported by the National Natural Science Foundation of China (Grant Nos. 51222210 and 11234013) and the One Hundred Talent Project of the Chinese Academy of Sciences.

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

    PubMed Central

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

    2016-01-01

    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. PMID:26984488

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

    PubMed

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

    2016-01-01

    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. PMID:26984488

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

    NASA Astrophysics Data System (ADS)

    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.

  20. Highly improved voltage efficiency of seawater battery by use of chloride ion capturing electrode

    NASA Astrophysics Data System (ADS)

    Kim, Kyoungho; Hwang, Soo Min; Park, Jeong-Sun; Han, Jinhyup; Kim, Junsoo; Kim, Youngsik

    2016-05-01

    Cost-effective and eco-friendly battery system with high energy density is highly desirable. Herein, we report a seawater battery with a high voltage efficiency, in which a chloride ion-capturing electrode (CICE) consisting of Ag foil is utilized as the cathode. The use of Ag as the cathode leads to a sharp decrease in the voltage gaps between charge and discharge curves, based on reversible redox reaction of Ag/AgCl (at ∼2.9 V vs. Na+/Na) in a seawater catholyte during cycling. The Ag/AgCl reaction proves to be highly reversible during battery cycling. The battery employing the Ag electrode shows excellent cycling performance with a high Coulombic efficiency (98.6-98.7%) and a highly improved voltage efficiency (90.3% compared to 73% for carbonaceous cathode) during 20 cycles (total 500 h). These findings demonstrate that seawater batteries using a CICE could be used as next-generation batteries for large-scale stationary energy storage plants.

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

    PubMed Central

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

    2016-01-01

    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. PMID:27297565

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

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

    2016-01-01

    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. PMID:27297565

  4. The Science of Electrode Materials for Lithium Batteries

    SciTech Connect

    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.

  5. Nafion coated sulfur-carbon electrode for high performance lithium-sulfur batteries

    NASA Astrophysics Data System (ADS)

    Tang, Qiwei; Shan, Zhongqiang; Wang, Li; Qin, Xue; Zhu, Kunlei; Tian, Jianhua; Liu, Xuesheng

    2014-01-01

    In this paper, a nafion coated electrode is prepared to improve the performance of lithium sulfur batteries. It is demonstrated from a series of measurements that the nafion layer is quite effective in reducing shuttle effect and enhancing the stability and the reversibility of the electrode. When measured under the rate of 0.2 C, the initial discharge capacity of the nafion coated electrode can reach 1084 mAh g-1, with a Columbic efficiency of about 100%. After 100 charge/discharge cycles, this electrode can also deliver a reversible capacity of as high as 879 mAh g-1. Significantly, the charge-transfer resistance of the electrode tends to be reducing after coated with an appropriate thickness of nafion film. The cation conductivity as well as anion inconductivity is considered to be the dominant factor for the superior electrochemical properties.

  6. Method of preparation of carbon materials for use as electrodes in rechargeable batteries

    DOEpatents

    Doddapaneni, N.; Wang, J.C.F.; Crocker, R.W.; Ingersoll, D.; Firsich, D.W.

    1999-03-16

    A method is described for producing carbon materials for use as electrodes in rechargeable batteries. Electrodes prepared from these carbon materials exhibit intercalation efficiencies of {approx_equal} 80% for lithium, low irreversible loss of lithium, long cycle life, are capable of sustaining a high rates of discharge and are cheap and easy to manufacture. The method comprises a novel two-step stabilization process in which polymeric precursor materials are stabilized by first heating in an inert atmosphere and subsequently heating in air. During the stabilization process, the polymeric precursor material can be agitated to reduce particle fusion and promote mass transfer of oxygen and water vapor. The stabilized, polymeric precursor materials can then be converted to a synthetic carbon, suitable for fabricating electrodes for use in rechargeable batteries, by heating to a high temperature in a flowing inert atmosphere. 4 figs.

  7. Method of preparation of carbon materials for use as electrodes in rechargeable batteries

    DOEpatents

    Doddapaneni, Narayan; Wang, James C. F.; Crocker, Robert W.; Ingersoll, David; Firsich, David W.

    1999-01-01

    A method of producing carbon materials for use as electrodes in rechargeable batteries. Electrodes prepared from these carbon materials exhibit intercalation efficiencies of .apprxeq.80% for lithium, low irreversible loss of lithium, long cycle life, are capable of sustaining a high rates of discharge and are cheap and easy to manufacture. The method comprises a novel two-step stabilization process in which polymeric precursor materials are stabilized by first heating in an inert atmosphere and subsequently heating in air. During the stabilization process, the polymeric precursor material can be agitated to reduce particle fusion and promote mass transfer of oxygen and water vapor. The stabilized, polymeric precursor materials can then be converted to a synthetic carbon, suitable for fabricating electrodes for use in rechargeable batteries, by heating to a high temperature in a flowing inert atmosphere.

  8. Surface modification of active material structures in battery electrodes

    DOEpatents

    Erickson, Michael; Tikhonov, Konstantin

    2016-02-02

    Provided herein are methods of processing electrode active material structures for use in electrochemical cells or, more specifically, methods of forming surface layers on these structures. The structures are combined with a liquid to form a mixture. The mixture includes a surface reagent that chemically reacts and forms a surface layer covalently bound to the structures. The surface reagent may be a part of the initial liquid or added to the mixture after the liquid is combined with the structures. In some embodiments, the mixture may be processed to form a powder containing the structures with the surface layer thereon. Alternatively, the mixture may be deposited onto a current collecting substrate and dried to form an electrode layer. Furthermore, the liquid may be an electrolyte containing the surface reagent and a salt. The liquid soaks the previously arranged electrodes in order to contact the structures with the surface reagent.

  9. Lightweight battery electrode and method of making it

    NASA Astrophysics Data System (ADS)

    Ferrando, William A.; Divecha, Amarnath P.

    1993-03-01

    A process for producing a lightweight electrode grid by exposing a heated mat of dense graphite fibers to Ni(CO)4 gas wherein the Ni(CO)4 decomposes upon contact with the graphite fibers depositing nickel metal coating on the graphic fibers is presented. The nickel coated graphite fibers are then sintered to form the grid. Nickel or cadmium electrodes are made by attaching a current collector to the grid and impregnating the grid with the appropriate nickel or cadmium active material.

  10. Effect of contact between a current collector and a polyacetylene electrode on electrochemical behavior in polyacetylene/lithium batteries

    NASA Astrophysics Data System (ADS)

    Chen, S.-A.; Chiou, Y.-C.

    1984-05-01

    Organic batteries with a polyacetylene film (PA) as the anode, a lithium strip as the cathode, and lithium perchlorate dissolved in propylene carbonate as the electrolyte are constructed. Charging and discharging characteristics of three batteries with different types of PA electrode are investigated. Type a PA electrode involves mechanical pressed contact of nickel gauze with the upper portion of the PA electrode; charging and discharging of the battery are difficult due to the semiconducting characteristic of the PA. Type b involves a PA film which has one side coated with a sputtered palladium (Pd) film; good contact of the Pd current collector with the PA electrode makes charging and discharging easily manageable. Type c involves an iodine-doped PA film; the battery is easily charged and discharged, but cleaning the surface of the lithium electrode is necessary after a few cycles.

  11. The effect of crystal orientation on the aluminum anodes of the aluminum-air batteries in alkaline electrolytes

    NASA Astrophysics Data System (ADS)

    Fan, Liang; Lu, Huimin; Leng, Jing; Sun, Zegao; Chen, Chunbo

    2015-12-01

    Recently, aluminum-air (Al-air) batteries have received attention from researchers as an exciting option for safe and efficient batteries. The electrochemical performance of Aluminum anode remains an active area of investigation. In this paper, the electrochemical properties of polycrystalline Al, Al (001), (110) and (111) single crystals are investigated using potentiodynamic polarization and electrochemical impedance spectroscopy (EIS) in 4 M NaOH and KOH. Hydrogen corrosion rates of the Al anodes are determined by hydrogen collection. Battery performance using the anodes is tested by constant current discharge at 10 mA cm-2. This is the first report showing that the electrochemical properties of Al are closely related to the crystallographic orientation in alkaline electrolytes. The (001) crystallographic plane has good corrosion resistance but (110) is more sensitive. Al (001) single crystals display higher anode efficiency and capacity density. Controlling the crystallographic orientation of the Al anode is another way to improve the performance of Al-air batteries in alkaline electrolytes.

  12. Production of zinc and manganese oxide particles by pyrolysis of alkaline and Zn-C battery waste.

    PubMed

    Ebin, Burçak; Petranikova, Martina; Steenari, Britt-Marie; Ekberg, Christian

    2016-05-01

    Production of zinc and manganese oxide particles from alkaline and zinc-carbon battery black mass was studied by a pyrolysis process at 850-950°C with various residence times under 1L/minN2(g) flow rate conditions without using any additive. The particular and chemical properties of the battery waste were characterized to investigate the possible reactions and effects on the properties of the reaction products. The thermodynamics of the pyrolysis process were studied using the HSC Chemistry 5.11 software. The carbothermic reduction reaction of battery black mass takes place and makes it possible to produce fine zinc particles by a rapid condensation, after the evaporation of zinc from a pyrolysis batch. The amount of zinc that can be separated from the black mass is increased by both pyrolysis temperature and residence time. Zinc recovery of 97% was achieved at 950°C and 1h residence time using the proposed alkaline battery recycling process. The pyrolysis residue is mainly MnO powder with a low amount of zinc, iron and potassium impurities and has an average particle size of 2.9μm. The obtained zinc particles have an average particle size of about 860nm and consist of hexagonal crystals around 110nm in size. The morphology of the zinc particles changes from a hexagonal shape to s spherical morphology by elevating the pyrolysis temperature. PMID:26547409

  13. Lead acid battery performance and cycle life increased through addition of discrete carbon nanotubes to both electrodes

    NASA Astrophysics Data System (ADS)

    Sugumaran, Nanjan; Everill, Paul; Swogger, Steven W.; Dubey, D. P.

    2015-04-01

    Contemporary applications are changing the failure mechanisms of lead acid batteries. Sulfation at the negative electrode, acid stratification, and dendrite formation now precede positive electrode failures such as grid corrosion and active material shedding. To attenuate these failures, carbon has been explored as a negative electrode additive to increase charge acceptance, eliminate sulfation, and extend cycle life. Frequently, however, carbon incorporation decreases paste density and hinders manufacturability. Discrete carbon nanotubes (dCNT), also known as Molecular Rebar®, are lead acid battery additives which can be stably incorporated into either electrode to increase charge acceptance and cycle life with no change to paste density and without impeding the manufacturing process. Here, full-scale automotive batteries containing dCNT in the negative electrode or both negative and positive electrodes are compared to control batteries. dCNT batteries show little change to Reserve Capacity, improved Cold Cranking, increased charge acceptance, and enhanced overall system efficiency. Life cycle tests show >60% increases when dCNT are incorporated into the negative electrode (HRPSoC/SBA) and up to 500% when incorporated into both electrodes (SBA), with water loss per cycle reduced >20%. Failure modes of cycled batteries are discussed and a hypothesis of dCNT action is introduced: the dCNT/Had Overcharge Reaction Mechanism.

  14. Advanced hydrogen electrode for hydrogen-bromide battery

    NASA Technical Reports Server (NTRS)

    Kosek, Jack A.; Laconti, Anthony B.

    1987-01-01

    Binary platinum alloys are being developed as hydrogen electrocatalysts for use in a hydrogen bromide battery system. These alloys were varied in terms of alloy component mole ratio and heat treatment temperature. Electrocatalyst evaluation, performed in the absence and presence of bromide ion, includes floating half cell polarization studies, electrochemical surface area measurements, X ray diffraction analysis, scanning electron microscopy analysis and corrosion measurements. Results obtained to date indicate a platinum rich alloy has the best tolerance to bromide ion poisoning.

  15. Battery and fuel cell electrodes containing stainless steel charging additive

    DOEpatents

    Zuckerbrod, David; Gibney, Ann

    1984-01-01

    An electrode for use in electrochemical energy cells is made, comprising a hydrophilic layer and a hydrophobic layer, where the hydrophilic layer comprises a hydrophilic composite which includes: (i) carbon particles; (ii) stainless steel particles; (iii) a nonwetting agent; and (iv) a catalyst, where at least one current collector contacts said composite.

  16. Microstructural effects on the average properties in porous battery electrodes

    NASA Astrophysics Data System (ADS)

    García-García, Ramiro; García, R. Edwin

    2016-03-01

    A theoretical framework is formulated to analytically quantify the effects of the microstructure on the average properties of porous electrodes, including reactive area density and the through-thickness tortuosity as observed in experimentally-determined tomographic sections. The proposed formulation includes the microstructural non-idealities but also captures the well-known perfectly spherical limit. Results demonstrate that in the absence of any particle alignment, the through-thickness Bruggeman exponent α, reaches an asymptotic value of α ∼ 2 / 3 as the shape of the particles become increasingly prolate (needle- or fiber-like). In contrast, the Bruggeman exponent diverges as the shape of the particles become increasingly oblate, regardless of the degree of particle alignment. For aligned particles, tortuosity can be dramatically suppressed, e.g., α → 1 / 10 for ra → 1 / 10 and MRD ∼ 40 . Particle size polydispersity impacts the porosity-tortuosity relation when the average particle size is comparable to the thickness of the electrode layers. Electrode reactivity density can be arbitrarily increased as the particles become increasingly oblate, but asymptotically reach a minimum value as the particles become increasingly prolate. In the limit of a porous electrode comprised of fiber-like particles, the area density decreases by 24% , with respect to a distribution of perfectly spherical particles.

  17. Calcium-bismuth electrodes for large-scale energy storage (liquid metal batteries)

    SciTech Connect

    Kim, H; Boysen, DA; Ouchi, T; Sadoway, DR

    2013-11-01

    Calcium is an attractive electrode material for use in grid-scale electrochemical energy storage due to its low electronegativity, earth abundance, and low cost. The feasibility of combining a liquid Ca-Bi positive electrode with a molten salt electrolyte for use in liquid metal batteries at 500-700 degrees C was investigated. Exhibiting excellent reversibility up to current densities of 200 mA cm(-2), the calcium bismuth liquid alloy system is a promising positive electrode candidate for liquid metal batteries. The measurement of low self-discharge current suggests that the solubility of calcium metal in molten salt electrolytes can be sufficiently suppressed to yield high coulombic efficiencies >98%. The mechanisms giving rise to Ca-Bi electrode overpotentials were investigated in terms of associated charge transfer and mass transport resistances. The formation of low density Ca11Bi10 intermetallics at the electrode electrolyte interface limited the calcium deposition rate capability of the electrodes; however, the co-deposition of barium into bismuth from barium-containing molten salts suppressed Ca-Bi intermetallic formation thereby improving the discharge capacity. (C) 2013 Elsevier B.V. All rights reserved.

  18. In Situ Powder Diffraction Studies of Electrode Materials in Rechargeable Batteries.

    PubMed

    Sharma, Neeraj; Pang, Wei Kong; Guo, Zaiping; Peterson, Vanessa K

    2015-09-01

    The ability to directly track the charge carrier in a battery as it inserts/extracts from an electrode during charge/discharge provides unparalleled insight for researchers into the working mechanism of the device. This crystallographic-electrochemical information can be used to design new materials or modify electrochemical conditions to improve battery performance characteristics, such as lifetime. Critical to collecting operando data used to obtain such information in situ while a battery functions are X-ray and neutron diffractometers with sufficient spatial and temporal resolution to capture complex and subtle structural changes. The number of operando battery experiments has dramatically increased in recent years, particularly those involving neutron powder diffraction. Herein, the importance of structure-property relationships to understanding battery function, why in situ experimentation is critical to this, and the types of experiments and electrochemical cells required to obtain such information are described. For each battery type, selected research that showcases the power of in situ and operando diffraction experiments to understand battery function is highlighted and future opportunities for such experiments are discussed. The intention is to encourage researchers to use in situ and operando techniques and to provide a concise overview of this area of research. PMID:26223736

  19. Effects of acetone on electrooxidation of 2-propanol in alkaline medium on the Pd/Ni-foam electrode

    NASA Astrophysics Data System (ADS)

    Cheng, Yuanhui; Liu, Yao; Cao, Dianxue; Wang, Guiling; Gao, Yinyi

    2011-03-01

    Acetone is the main product of 2-propanol electrooxidation in both acid and alkaline electrolytes; it always co-exists with 2-propanol in the reaction solution due to its liquid nature. Whether acetone will affect the electrooxidation of 2-propanol has not been well documented, which is a key issue that needs to be addressed for the direct 2-propanol fuel cell. In this study, the influence of acetone on the electrooxidation of 2-propanol in alkaline medium is investigated, using state-of-the-art Pd electrode, by cyclic voltammetry and chronoamperometry. The electrode is prepared using a chemical replacement method, by dipping nickel foam into acidified PdCl2 solution, and characterized by scanning electron microscopy. We found that the presence of acetone adversely affects electrooxidation performance of 2-propanol and substantially reduces the oxidation current of 2-propanol on Pd in alkaline medium. The acetone poisoning effect is interpreted by a competitive adsorption mechanism, in which acetone adsorbs onto Pd surface and occupies the active sites for 2-propanol electrooxidation, leading to a significant decrease in the number of these sites for 2-propanol electrooxidation. The results of this study point out that efficient electrocatalysts for 2-propanol electrooxidation in alkaline electrolytes must be non-adsorptive to acetone besides being highly active to 2-propanol oxidation.

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

    NASA Astrophysics Data System (ADS)

    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

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed Central

    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.

    2016-01-01

    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. PMID:27270184

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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

    2016-01-01

    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. PMID:27270184

  6. Mesoporous α-MnO 2/Pd catalyst air electrode for rechargeable lithium-air battery

    NASA Astrophysics Data System (ADS)

    Thapa, Arjun Kumar; Ishihara, Tatsumi

    Rechargeable lithium-air battery is studied using Pd/mesoporous α-MnO 2 air composite electrode. In the present work, we have studied the preparation and electrochemical performance of ordered mesoporous α-MnO 2 as a cathode catalyst for rechargeable Li-air batteries. α-MnO 2 was prepared by reduction of KMnO 4 solution in acidic aqueous solution followed by successive proton and alkali-ion exchange method. α-MnO 2 with high surface area of 33-133.0 m 2 g -1 was successively synthesized and used as an electrode catalyst for Li-air battery. It was found that the mixture of Pd and mesoporous α-MnO 2 electrode shows the high activity to oxidation and reduction of Li to form Li 2O 2 or Li 2O. Application of Pd/mesoporous α-MnO 2, which is mixed with teflonized acetylene binder (TAB), for air electrode is effective for decreasing the charge potential and also improved the energy efficiency as well as cyclability.

  7. Regulated Breathing Effect of Silicon Negative Electrode for Dramatically Enhanced Performance of Li-Ion Battery

    SciTech Connect

    Xiao, Xingcheng; Zhou, Weidong; Kim, Youngnam; Ryu, Ill; Gu, Meng; Wang, Chong M.; Liu, Gao; Liu, Zhongyi; Gao, Huajian

    2015-03-01

    Si is an attractive negative electrode material for lithium ion batteries due to its high specifi c capacity (≈3600 mAh g –1 ). However, the huge volume swelling and shrinking during cycling, which mimics a breathing effect at the material/electrode/cell level, leads to several coupled issues including fracture of Si particles, unstable solid electrolyte interphase, and low Coulombic effi ciency. In this work, the regulation of the breathing effect is reported by using Si–C yolk–shell nanocomposite which has been well-developed by other researchers. The focus is on understanding how the nanoscaled materials design impacts the mechanical and electrochemical response at electrode level. For the fi rst time, it is possible to observe one order of magnitude of reduction on breathing effect at the electrode level during cycling: the electrode thickness variation reduced down to 10%, comparing with 100% in the electrode with Si nanoparticles as active materials. The Si–C yolk–shell nanocomposite electrode exhibits excellent capacity retention and high cycle effi ciency. In situ transmission electron microscopy and fi nite element simulations consistently reveals that the dramatically enhanced performance is associated with the regulated breathing of the Si in the new composite, therefore the suppression of the overall electrode expansion.

  8. Characteristics of the high-rate discharge capability of a nickel/metal hydride battery electrode

    SciTech Connect

    Geng, M.; Han, J.; Feng, F.; Northwood, D.O.

    1999-10-01

    The high rate discharge capability of the negative electrode in a Ni/MH battery is mainly determined by the charge transfer process at the interface between the metal hydride (MH) alloy powder and the electrolyte, and the mass transfer process in the bulk MH alloy powder. In this study, the anodic polarization curves of a MH electrode were measured and analyzed. An alloy of nominal composition Mm{sub 0.95}Ti{sub 0.05}Ni{sub 3.85}Co{sub 0.45}Mn{sub 0.35}Al{sub 0.35} was used as the negative electrode material. With increasing number of charge/discharge cycles, the MH alloy powders microcrack into particles several micrometers in diameter. The decrease in the MH alloy particle size results in an increase in both the activation surface area and the exchange current density of the MH alloy electrode. The electrode overpotentials of the MH electrode decreases with increasing number of cycles at a large value of anodic polarization current. The decrease in electrode overpotential leads to an increase in the high rate discharge capability of the MH electrode. By using the limiting current, the hydrogen diffusion coefficient in the MH alloy was estimated to be 1.2 x 10{sup {minus}11}cm{sup 2}s{sup {minus}1} assuming an average particle radius of 5 {micro}m.

  9. Lightweight battery electrode and method of making it

    NASA Astrophysics Data System (ADS)

    Ferrando, William A.; Divecha, Amarnath P.

    1994-11-01

    A process is introduced for producing a lightweight electrode grid by exposing a compressed, heated mat of dense graphite fibers to Ni(CO)4 gas wherein the Ni(CO)4 decomposes upon contact with the graphite fibers depositing a nickel metal coating on the graphite fibers which strongly bonds the fibers together to form a compressed mat or grid of nickel metal coated fibers.

  10. Polyacrylate bound TiSb2 electrodes for Li-ion batteries

    NASA Astrophysics Data System (ADS)

    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.

  11. Composite polymer positive electrodes in solid-state lithium secondary batteries

    SciTech Connect

    Novak, P.; Inganas, O.; Bjorklund, R.

    1987-06-01

    The authors have developed composite polymer electrodes for use in all solid-state batteries in combination with Li. The composite is formed from water soluble polypyrrole which is combined with the solid polymer electrolyte polyethylene oxide. The composite electrode shows enhanced coulombic capacity as compared to an electrode composed only of the electroactive material, polypyrrole. Coulombic efficiency is good (90-95%) and energy efficiency is acceptable (80-85%) in galvanostatic studies. Charge retention is rather poor due to self-discharge. They have obtained proof that the electroactivity is due to polypyrrole, through the use of in situ spectroelectrochemical studies. They have characterized the composite electrode using scanning electron microscopy and conductive measurements.

  12. Combined operando studies of new electrode materials for Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Jumas, Jean-Claude; Sougrati, Moulay Tahar; Perea, Alexis; Aldon, Laurent; Olivier-Fourcade, Josette

    2013-04-01

    The performances of Li-ion batteries depend on many factors amongst which the important ones are the electrode materials and their structural and electronic evolution upon cycling. For a better understanding of lithium reactivity mechanism of many materials the combination of X-Ray Powder Diffraction (XRPD) and Transmission Mössbauer Spectroscopy (TMS) providing both structural and electronic information during the electrochemical cycling has been carried out. Thanks to the design of a specific electrochemical cell, derived from a conventional Swagelock cell, such measurements have been realised in operando mode. Two examples illustrate the greatness of combining XRPD and TMS for the study of LiFe0.75Mn0.25PO4 as positive electrode and TiSnSb as negative electrode. Different kinds of insertion or conversion reactions have been identified leading to a better optimization and design of performing electrodes.

  13. A stable graphite negative electrode for the lithium-sulfur battery.

    PubMed

    Jeschull, Fabian; Brandell, Daniel; Edström, Kristina; Lacey, Matthew J

    2015-12-14

    Efficient, reversible lithium intercalation into graphite in ether-based electrolytes is enabled through a protective electrode binder, polyacrylic acid sodium salt (PAA-Na). In turn, this enables the creation of a stable "lithium-ion-sulfur" cell, using a lithiated graphite negative electrode with a sulfur positive electrode, using the common DME:DOL solvent system suited to the electrochemistry of the lithium-sulfur battery. Graphite-sulfur lithium-ion cells show average coulombic efficiencies of ∼99.5%, compared with <95% for lithium-sulfur cells, and significantly better capacity retention, taking into account cell balancing considerations. The high efficiency derives from the considerably better interfacial stability of the graphite electrode, which suppresses the polysulfide redox shuttle and self-discharge. PMID:26451894

  14. Recovery of MnO2 from a spent alkaline battery leach solution via ozone treatment

    NASA Astrophysics Data System (ADS)

    Cruz-Díaz, Martín R.; Arauz-Torres, Yennifer; Caballero, Francisco; Lapidus, Gretchen T.; González, Ignacio

    2015-01-01

    This work investigates the reaction rate of Mn(II) to generate solid manganese dioxide (MnO2) as a function of the gaseous ozone mass flow rate (27.5-77 g h-1). The experimental studies were carried out in a semi-continuous reactor, using a synthetic solution (300 mL of 1 M H2SO4 with 6000 ppm of Mn(II) added as MnSO4) that simulated the composition of an acid leaching solution from spent alkaline battery material (SBM). It was observed that at 1.3-1.45 V/SHE and pH < 1.0 a selective formation of MnO2 powder was obtained; at values greater than 1.45 V/SHE, permanganate ion (MnO41-) was formed. On the other hand, a linear relation was perceived between the volumetric mass transfer coefficient (kLa) and the ozone mass flow rate (19.3-77 g h-1 in 600 mL of the 1 M H2SO4 solution). The rate constant (k) was determined in the presence and absence of nonporous plastic spheres (D = 3 mm). In both cases the rate of Mn(II) conversion increased proportionally with the ozone mass flow rate, although the conversions obtained with non-porous plastic spheres (x = 82%) were always higher than those without non-porous plastic spheres (x = 72%). A pseudo-homogenous mass transfer model adequately approximated the experimental data.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. Performance and mechanism of FeSb2 as negative electrode for Na-ion batteries

    NASA Astrophysics Data System (ADS)

    Darwiche, Ali; Toiron, Matthieu; Sougrati, Moulay T.; Fraisse, Bernard; Stievano, Lorenzo; Monconduit, Laure

    2015-04-01

    For the first time, cycling capability and life analysis of the FeSb2/Na battery are tested. Thanks to an appropriate carboxymethyl cellulose/carbon formulation, this electrode exhibits excellent electrochemical performances as negative electrode material for Sodium-Ion Batteries (SIB), sustaining a reversible capacity exceeding 540 and 440 mAh/g over more than 130 cycles at a current of 36 and 300 mA/g, respectively. Such performances overtake those of Sb in terms of cyclability under high rate, one of the best negative electrodes reported to date for SIB. In situ X-ray diffraction and low temperature Mössbauer spectroscopy analyses indicate that the reaction mechanism of the first sodiation of FeSb2 is based on a conversion reaction, leading to the formation of a very efficient Na3Sb/metallic Fe0 nanosized electrode with an excellent capacity retention at relatively high rate. The reaction mechanism after the first discharge is based on a reversible alloying reaction (2Na3Sb ↔ 2Sb + 6Na), where iron is no more involved. The role of Fe appears however to be crucial in the excellent cycling performances, likely due to the increase of the electronic conductivity brought both by its nanosized nature and its homogenous distribution in the electrode.

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

    PubMed Central

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

    2016-01-01

    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. PMID:27025781

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

    PubMed

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

    2016-01-01

    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(-1)electrode (∼393 mAh cm(-3)electrode) 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. PMID:27025781

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

    NASA Astrophysics Data System (ADS)

    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.

  20. Potentiostatic and ac impedance studies of the hydrogen electrodes used in Ni/H2 batteries

    NASA Technical Reports Server (NTRS)

    Le Helloco, Jean-Guy; Bojkov, Hristo; Parthasarathy, Arvind; Srinivasan, Supramaniam; Appleby, A. J.

    1992-01-01

    In a study of electrode activity for hydrogen evolution and hydrogen ionization, knowledge of the detailed kinetics and of the surface coverage by adsorbed hydrogen is essential. In the Ni/H2 battery, the hydrogen electrode is subjected to high hydrogen pressure; elucidation of the variation of kinetic parameters with hydrogen pressure is therefore of interest. Potentiostatic and ac impedance spectroscopic techniques were used in the present study. The equivalent circuit of the reaction, the kinetic parameters, and their pressure dependence have been determined.

  1. Hydraulically refueled battery employing a packed bed metal particle electrode

    SciTech Connect

    Siu, S.C.; Evans, J.W.

    1998-12-15

    A secondary zinc air cell, or another selected metal air cell, employing a spouted/packed metal particle bed and an air electrode is described. More specifically, two embodiments of a cell, one that is capable of being hydraulically recharged, and a second that is capable of being either hydraulically or electrically recharged. Additionally, each cell includes a sloped bottom portion to cause stirring of the electrolyte/metal particulate slurry when the cell is being hydraulically emptied and refilled during hydraulically recharging of the cell. 15 figs.

  2. Hydraulically refueled battery employing a packed bed metal particle electrode

    SciTech Connect

    Siu, Stanley C.; Evans, James W.

    1998-01-01

    A secondary zinc air cell, or another selected metal air cell, employing a spouted/packed metal particle bed and an air electrode. More specifically, two embodiments of a cell, one that is capable of being hydraulically recharged, and a second that is capable of being either hydraulically or electrically recharged. Additionally, each cell includes a sloped bottom portion to cause stirring of the electrolyte/metal particulate slurry when the cell is being hydraulically emptied and refilled during hydraulically recharging of the cell.

  3. Silicon Nanowire Fabric as a Lithium Ion Battery Electrode Material

    SciTech Connect

    Chockla, Aaron M.; Harris, Justin T.; Akhavan, Vahid A.; Bogart, Timothy D.; Holmberg, Vincent C.; Steinhagen, Chet; Mullins, C. Buddie; Stevenson, Keith J.; Korgel, Brian A.

    2011-11-09

    A nonwoven fabric with paperlike qualities composed of silicon nanowires is reported. The nanowires, made by the supercritical-fluid–liquid–solid process, are crystalline, range in diameter from 10 to 50 nm with an average length of >100 μm, and are coated with a thin chemisorbed polyphenylsilane shell. About 90% of the nanowire fabric volume is void space. Thermal annealing of the nanowire fabric in a reducing environment converts the polyphenylsilane coating to a carbonaceous layer that significantly increases the electrical conductivity of the material. This makes the nanowire fabric useful as a self-supporting, mechanically flexible, high-energy-storage anode material in a lithium ion battery. Anode capacities of more than 800 mA h g{sup –1} were achieved without the addition of conductive carbon or binder.

  4. Recovery of manganese oxides from spent alkaline and zinc-carbon batteries. An application as catalysts for VOCs elimination.

    PubMed

    Gallegos, María V; Falco, Lorena R; Peluso, Miguel A; Sambeth, Jorge E; Thomas, Horacio J

    2013-06-01

    Manganese, in the form of oxide, was recovered from spent alkaline and zinc-carbon batteries employing a biohydrometallurgy process, using a pilot plant consisting in: an air-lift bioreactor (containing an acid-reducing medium produced by an Acidithiobacillus thiooxidans bacteria immobilized on elemental sulfur); a leaching reactor (were battery powder is mixed with the acid-reducing medium) and a recovery reactor. Two different manganese oxides were recovered from the leachate liquor: one of them by electrolysis (EMO) and the other by a chemical precipitation with KMnO4 solution (CMO). The non-leached solid residue was also studied (RMO). The solids were compared with a MnOx synthesized in our laboratory. The characterization by XRD, FTIR and XPS reveal the presence of Mn2O3 in the EMO and the CMO samples, together with some Mn(4+) cations. In the solid not extracted by acidic leaching (RMO) the main phase detected was Mn3O4. The catalytic performance of the oxides was studied in the complete oxidation of ethanol and heptane. Complete conversion of ethanol occurs at 200°C, while heptane requires more than 400°C. The CMO has the highest oxide selectivity to CO2. The results show that manganese oxides obtained using spent alkaline and zinc-carbon batteries as raw materials, have an interesting performance as catalysts for elimination of VOCs. PMID:23562448

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Hexagonal BC3 as a Robust Electrode Material for Li, Na, and K Ion Batteries

    NASA Astrophysics Data System (ADS)

    Joshi, Rajendra; Ozdemir, Burak; Peralta, Juan; Barone, Veronica

    We propose hexagonal BC3 as a robust electrode material for Li, Na, and K ion batteries based on first-principles density functional theory calculations. We show that, by intercalating Li, Na, and K in BC3, it is possible to form Li1.5BC3, Na1BC3, and K1.5BC3 which correspond to a high theoretical capacity of 858 mA h/g, 572 mA h/g, 858 mA h/g, respectively. In addition, this material presents small open circuit voltage variations of 0.49, 0.12, and 0.16 V when used as electrode for Li, Na, and K ion batteries, respectively. NSF CBET-1335944, NSF DMR-0906617, DOE DE-FG02-10ER16203.

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

    PubMed

    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. PMID:26915951

  8. Effect of electrode compression on the wettability of lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lee, Sang Gun; Jeon, Dong Hyup

    2014-11-01

    Using the multiphase lattice Boltzmann method (LBM), the electrolyte transport dynamics in the two-dimensional electrode structure of a lithium-ion battery are simulated. The effect of the compression ratio of a porous electrode on wettability is explored with respect to variations of porosity and particle shape. The electrolyte distribution in the electrode and the electrolyte saturation profile are examined in order to evaluate the wetting capability at various compression ratios. The results show that wettability in the electrode decreases as the compression ratio increases. In a highly compressed electrode, the through-plane permeation of liquid electrolyte is small. Thus, the electrolytes are mainly observed at the interface of the electrode and separator. The anode has lower wettability than the cathode due to the deformation of particle shape during the manufacturing process. Therefore, particle shape has a strong effect on wettability. The two-dimensional LBM approach used in this study characterizes the electrolyte transport phenomena inside the electrode and allows us to compare the wettability between the cathode and anode at various compression ratios.

  9. Hydridable material for the negative electrode in a nickel-metal hydride storage battery

    DOEpatents

    Knosp, Bernard; Bouet, Jacques; Jordy, Christian; Mimoun, Michel; Gicquel, Daniel

    1997-01-01

    A monophase hydridable material for the negative electrode of a nickel-metal hydride storage battery with a "Lave's phase" structure of hexagonal C14 type (MgZn.sub.2) has the general formula: Zr.sub.1-x Ti.sub.x Ni.sub.a Mn.sub.b Al.sub.c Co.sub.d V.sub.e where ##EQU1##

  10. 3D Porous Sponge-Inspired Electrode for Stretchable Lithium-Ion Batteries.

    PubMed

    Liu, Wei; Chen, Zheng; Zhou, Guangmin; Sun, Yongming; Lee, Hye Ryoung; Liu, Chong; Yao, Hongbin; Bao, Zhenan; Cui, Yi

    2016-05-01

    A stretchable Li4 Ti5 O12 anode and a LiFePO4 cathode with 80% stretchability are prepared using a 3D interconnected porous polydimethylsiloxane sponge based on sugar cubes. 82% and 91% capacity retention for anode and cathode are achieved after 500 stretch-release cycles. Slight capacity decay of 6% in the battery using the electrode in stretched state is observed. PMID:26992146

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

    NASA Astrophysics Data System (ADS)

    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.

  12. Chemical modification approaches for improved performance of Na-ion battery electrodes

    NASA Astrophysics Data System (ADS)

    Byles, Bryan; Clites, Mallory; Pomerantseva, Ekaterina

    2015-08-01

    Na-ion batteries have received considerable attention in recent years but still face performance challenges such as limited cycle lifetime and low capacities at high current rates. In this work, we propose novel combinations of preand post-synthesis treatments to modify known Na-ion battery electrode materials to achieve enhanced electrochemical performance. We work with two model metal oxide materials to demonstrate the effectiveness of the different treatments. First, wet chemical preintercalation is combined with post-synthesis aging, hydrothermal treatment, and annealing of α-V2O5, resulting in enhanced capacity retention in a Na-ion battery system. The hydrothermal treatment resulted in an increased specific capacity of nearly 300 mAh/g. Second, post-synthesis acid leaching is performed on α- MnO2, also resulting in improved electrochemical capacity. The chemical, structural, and morphological changes brought about by the modifications are fully characterized.

  13. Assembly of a Robust and Economical MnO[subscript2]-Based Reference Electrode

    ERIC Educational Resources Information Center

    Masse´, Robert C.; Gerken, James B.

    2015-01-01

    There is a dearth of base-stable reference electrodes that are suitable for use by students in a teaching laboratory or undergraduate research context. To remedy this, we have developed a technique to produce reference electrodes suitable for alkaline environments. By utilizing components of a commercially available alkaline-type battery, an…

  14. Electrode-supported thin α-alumina separators for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Mi, Wanliang; Sharma, Gaurav; Dong, Xueliang; Jin, Yi; Lin, Y. S.

    2016-02-01

    Lithium ion batteries with an inorganic separator offer improved safety and enhanced reliability. The free-standing inorganic separators recently studied for lithium ion batteries are brittle and expensive. To address these issues, this paper reports the synthesis of a new and stable electrode-supported separator using a low-cost ceramic powder. Thin and porous α-Al2O3 separator films of thicknesses down to 40 μm were coated on Li4Ti5O12 (LTO) electrode by blade-coating a slurry of α-Al2O3, water and a small amount of polyvinyl alcohol (PVA). The performance of the LTO/Li cells with coated α-Al2O3 separator improves with decreasing PVA content. Cells with coated α-Al2O3 separator containing 0.4wt% PVA exhibit similar discharge capacity but better rate capability than those with commercial polypropylene (PP) or thick sintered α-Al2O3 separator. The coated α-Al2O3 separator does not react with LTO even after many charge/discharge cycles. Fabrication of the electrode-supported α-Al2O3 separator is scalable and cost-effective, offering high potential for practical application in industrial lithium ion battery manufacturing.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. Performance of AA5052 alloy anode in alkaline ethylene glycol electrolyte with dicarboxylic acids additives for aluminium-air batteries

    NASA Astrophysics Data System (ADS)

    Wang, DaPeng; Zhang, DaQuan; Lee, KangYong; Gao, LiXin

    2015-11-01

    Dicarboxylic acid compounds, i.e. succinic acid (SUA), adipic acid (ADA) and sebacic acid (SEA), are used as electrolyte additives in the alkaline ethylene glycol solution for AA5052 aluminium-air batteries. It shows that the addition of dicarboxylic acids lowers the hydrogen gas evolution rate of commercial AA5052 aluminium alloy anode. AA5052 aluminium alloy has wide potential window for electrochemical activity and better discharge performance in alkaline ethylene glycol solution containing dicarboxylic acid additives. ADA has the best inhibition effect for the self-corrosion of AA5052 anode among the three dicarboxylic acid additives. Fourier transform infrared spectroscopy (FT-IR) reveals that dicarboxylic acids and aluminium ions can form coordination complexes. Quantum chemical calculations shows that ADA has a smaller energy gap (ΔE, the energy difference between the lowest unoccupied orbital and the highest occupied orbital), indicating that ADA has the strongest interaction with aluminium ions.

  17. Carbon-Rich Active Materials with Macrocyclic Nanochannels for High-Capacity Negative Electrodes in All-Solid-State Lithium Rechargeable Batteries.

    PubMed

    Sato, Sota; Unemoto, Atsushi; Ikeda, Takuji; Orimo, Shin-Ichi; Isobe, Hiroyuki

    2016-07-01

    A high-capacity electrode active material with macrocyclic nanochannels is developed for a negative electrode of lithium batteries. With appropriate design of the molecular and crystal structures, a ubiquitous chemical commonly available in reagent stocks of any chemistry laboratories, naphthalene, was transformed into a high-performance electrode material for all-solid-state lithium batteries. PMID:27173002

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

    NASA Astrophysics Data System (ADS)

    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. Cu2Sb thin film electrodes prepared by pulsed laser deposition f or lithium batteries

    SciTech Connect

    Song, Seung-Wan; Reade, Ronald P.; Cairns, Elton J.; Vaughey, Jack T.; Thackeray, Michael M.; Striebel, Kathryn A.

    2003-08-01

    Thin films of Cu2Sb, prepared on stainless steel and copper substrates with a pulsed laser deposition technique at room temperature, have been evaluated as electrodes in lithium cells. The electrodes operate by a lithium insertion/copper extrusion reaction mechanism, the reversibility of which is superior when copper substrates are used, particularly when electrochemical cycling is restricted to the voltage range 0.65-1.4 V vs. Li/Li+. The superior performance of Cu2Sb films on copper is attributed to the more active participation of the extruded copper in the functioning of the electrode. The continual and extensive extrusion of copper on cycling the cells leads to the isolation of Li3Sb particles and a consequent formation of Sb. Improved cycling stability of both types of electrodes was obtained when cells were cycled between 0.65 and 1.4 V. A low-capacity lithium-ion cell with Cu2Sb and LiNi0.8Co0.15Al0.05O2 electrodes, laminated from powders, shows excellent cycling stability over the voltage range 3.15 - 2.2 V, the potential difference corresponding to approximately 0.65-1.4 V for the Cu2Sb electrode vs. Li/Li+. Chemical self-discharge of lithiated Cu2Sb electrodes by reaction with the electrolyte was severe when cells were allowed to relax on open circuit after reaching a lower voltage limit of 0.1 V. The solid electrolyte interphase (SEI) layer formed on Cu2Sb electrodes after cells had been cycled between 1.4 and 0.65 V vs. Li/Li+ was characterized by Fourier-transform infrared spectroscopy; the SEI layer contributes to the large irreversible capacity loss on the initial cycle of these cells. The data contribute to a better understanding of the electrochemical behavior of intermetallic electrodes in rechargeable lithium batteries.

  20. Rechargeable zinc cell with alkaline electrolyte which inhibits shape change in zinc electrode

    DOEpatents

    Adler, Thomas C.; McLarnon, Frank R.; Cairns, Elton J.

    1994-01-01

    An improved rechargeable zinc cell is described comprising a zinc electrode and another electrode such as, for example, a nickel-containing electrode, and having an electrolyte containing KOH and a combination of KF and K.sub.2 CO.sub.3 salts which inhibits shape change in the zinc electrode, i.e., the zinc electrode exhibits low shape change, resulting in an improved capacity retention of the cell over an number of charge-discharge cycles, while still maintaining high discharge rate characteristics.

  1. Rechargeable zinc cell with alkaline electrolyte which inhibits shape change in zinc electrode

    DOEpatents

    Adler, T.C.; McLarnon, F.R.; Cairns, E.J.

    1994-04-12

    An improved rechargeable zinc cell is described comprising a zinc electrode and another electrode such as, for example, a nickel-containing electrode, and having an electrolyte containing KOH and a combination of KF and K[sub 2]CO[sub 3] salts which inhibits shape change in the zinc electrode, i.e., the zinc electrode exhibits low shape change, resulting in an improved capacity retention of the cell over an number of charge-discharge cycles, while still maintaining high discharge rate characteristics. 8 figures.

  2. Performance of the “SiO”-carbon composite-negative electrodes for high-capacity lithium-ion batteries; prototype 14500 batteries

    NASA Astrophysics Data System (ADS)

    Yamada, Masayuki; Uchitomi, Kazutaka; Ueda, Atsushi; Matsumoto, Kazunobu; Ohzuku, Tsutomu

    2013-03-01

    Prototype 14500 batteries (14 mm dia. and 50 mm hgt.; AA size) consisted of the “SiO”-carbon composite-negative and LiCo1/3Ni1/3Mn1/3O2/LiCoO2 (7/3 by weight)-positive electrodes were designed, fabricated and examined in voltage ranging from 2.5 to 4.2 V at -20, -10, 0, and +23 °C. The batteries were stored and delivered 1 Ah at 200 mA and 0.96 Ah at 2 A, and the capacity remained after 300 cycles at 23 °C was 0.7 Ah. Abuse tests, such as overcharging to 12 V, nail penetration, and heating of fully charged batteries in an oven at 150 °C, were also carried out and shown that the batteries showed neither smoke nor fire for all the tests examined. The battery performance was compared to that of conventional batteries with graphite-negative electrodes in the same size and the characteristic features of the lithium-ion batteries with the SiO-carbon composite-negative electrodes were discussed from the experimental results.

  3. An in situ operando MEMS platform for characterization of Li-ion battery electrodes

    NASA Astrophysics Data System (ADS)

    Jung, H.; Gerasopoulos, K.; Zhang, X.; Ghodssi, R.

    2015-12-01

    This paper presents an in situ operando approach that allows characterization of lithium-ion battery electrodes. A MEMS sensor is designed and integrated with a commercially available Raman spectroscope to enable monitoring the stress and structural changes in the electrodes. An interferometric method with an enhanced image processing algorithm is applied for analyzing the crystal phase-dependent stress changes - contributing to higher sensitivity compared to a previously reported technique - while the structural changes are monitored using Raman spectroscopy. New capabilities of our platform are highlighted, allowing visual observation of crystal phase-dependent structural changes in the electrode. Simultaneous characterization of the stress and structural changes are achieved concurrently in situ operando. The results show excellent agreement with previous literature reports on both phenomena.

  4. Binder-free nitrogen-doped carbon nanotubes electrodes for lithium-oxygen batteries

    NASA Astrophysics Data System (ADS)

    Lin, Xiujing; Lu, Xu; Huang, Tao; Liu, Zhaolin; Yu, Aishui

    2013-11-01

    Here the binder-free nickel foam supported nitrogen-doped carbon nanotubes (N-CNTs@Ni) are synthesized by a floating catalyst chemical vapor deposition (FCCVD) method. Without any additional treatment, it could be employed as the air electrode in the lithium-oxygen batteries and delivers 1814 mAh g-1 (normalized to the weight of the air electrode) at the current density of 0.05 mA cm-2. The loose packing 3-dimension network structure facilitates the O2 diffusion in the inner electrode and provides enough void volume for the products deposition during discharge process. The improved contact between N-CNTs and the current collector Ni is beneficial to suppress the volume expansion and leads to less polarization as well as good cycling performance.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    Liu, Jian; Sun, Xueliang

    2015-01-16

    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. PMID:25514580

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed

    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. PMID:24989450

  11. Engineering study on TiSnSb-based composite negative electrode for Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Wilhelm, H. A.; Marino, C.; Darwiche, A.; Soudan, P.; Morcrette, M.; Monconduit, L.; Lestriez, B.

    2015-01-01

    Micrometric TiSnSb is a promising negative electrode material for Li-ion batteries when formulated with carboxymethyl cellulose (CMC) binder and a mixture of carbon black and carbon nanofibers, and cycled in a fluoroethylene carbonate (FEC)-containing electrolyte. Here, other binder systems were evaluated, polyacrylic acid (PAAH) mixed with CMC, CMC in buffered solution at pH 3 and amylopectin. However CMC showed the better performance in terms of cycle life of the electrode. Whatever the binder, cycle life decreases with increasing the active mass loading, which is attributed to both the precipitation of liquid electrolyte degradation products and to the loss of electrical contacts within the composite electrode and with the current collector as a consequence of the active particles volume variations. Furthermore, calendaring the electrode unfortunately decreases the cycle life. The rate performance was studied as a function of the active mass loading and was shown to be determined by the electrode polarization resistance. Finally, full cells cycling tests with Li1Ni1/3Co1/3Mn1/3O2 at the positive electrode were done. 60% of the capacity is retained after 200 cycles at the surface capacity of 2.7 mAh cm-2.

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

    NASA Astrophysics Data System (ADS)

    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.

  13. A lead-film electrode on an aluminium substrate to serve as a lead-acid battery plate

    NASA Astrophysics Data System (ADS)

    Yolshina, L. A.; Kudyakov, V. Ya; Zyryanov, V. G.

    Compact lead layers have been deposited on the surfaces of aluminium and aluminium alloys. These coatings are uniform in thickness and have high porosity. The lead-film electrode produced on aluminium plate can be used as the positive electrode in a lead-acid battery.

  14. Lead-acid bipolar battery assembled with primary chemically formed positive pasted electrode

    NASA Astrophysics Data System (ADS)

    Karami, H.; Shamsipur, M.; Ghasemi, S.; Mousavi, M. F.

    Primary chemically formed lead dioxide (PbO 2) was used as positive electrode in preparation of lead-acid bipolar batteries. Chemical oxidation was carried out by both mixing and dipping methods using an optimized amount of ammonium persulfate as a suitable oxidizing agent. X-ray diffraction studies showed that the weight ratio of β-PbO 2 to α-PbO 2 is more for mixing method before electrochemical forming. The electrochemical impedance spectroscopy (EIS) was used to investigate charge transfer resistance of the lead dioxide obtained by mixing and dipping methods before and after electrochemical forming. Four types of bipolar lead-acid batteries were produced with: (1) lead substrate and conventional electroforming; (2) carbon doped polyethylene substrate with conventional electroforming; (3) carbon doped polyethylene substrate with chemical forming after curing and drying steps in oxidant bath, followed by electrochemical forming, and (4) carbon doped polyethylene substrate with primary chemical oxidation in mixing step, followed by conventional electroforming. The capacity and cycle-life tests of the prepared bipolar batteries were performed by a home-made battery tester and using the pulsed current method. The prepared batteries showed low weight, high capacity, high energy density and high power density. The first capacities of bipolar batteries of type 1-4 were found to be 152, 150, 180 and 198 mAh g -1, respectively. The experimental results showed that the prepared 6 V bipolar batteries of type 1-4 have power density (per cell unit) of 59.7, 57.4, 78.46 and 83.30 mW g -1 (W kg -1), respectively.

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

    NASA Astrophysics Data System (ADS)

    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.

  16. Performance evaluation of a membraneless divergent electrode-flow-through (DEFT) alkaline electrolyser based on optimisation of electrolytic flow and electrode gap

    NASA Astrophysics Data System (ADS)

    Gillespie, M. I.; van der Merwe, F.; Kriek, R. J.

    2015-10-01

    A membraneless divergent electrode-flow-through (DEFT) alkaline electrolysis design and operating principle is investigated, which allows for the ohmic drop contribution and performance threshold limitations of a conventional membrane barrier to be overcome. Employing mesh electrodes of 30 mm diameter, operation of the electrolyser at an electrolytic flow velocity of 0.075-0.1 m s-1, resulted in an optimal electrode gap of ∼2.5 mm, while operating at greater velocities (>0.1-0.2 m s-1) allows for the employment of a smaller optimal gap of ∼0.8 mm. At an electrode gap of 2.5 mm and current densities of 3500 mA cm-2, hydrogen purity of 99.83% has been recorded. With pure nickel electrodes current densities of 101.19 mA cm-2 (at 1.80 VDC) and 326.33 mA cm-2 (at 2 VDC) have been achieved, while the use of superior catalysts, namely, RuO2/IrO2/TiO2 and Pt for the anode and cathode respectively, resulted in the current densities to increase to 219.99 mA cm-2 (at 1.8 VDC) and 474.40 mA cm-2 (at 2 VDC) at an electrode gap of 2.5 mm and a minimum flow velocity of 0.075 m s-1. The test rig is capable of generating hydrogen at a rate of 63.6 L/hr at normal temperature and pressure (NTP). The production rate follows current density linearly at high overpotentials.

  17. Chemically and compositionally modified solid solution disordered multiphase nickel hydroxide positive electrode for alkaline rechargeable electrochemical cells

    DOEpatents

    Ovshinsky, Stanford R.; Corrigan, Dennis; Venkatesan, Srini; Young, Rosa; Fierro, Christian; Fetcenko, Michael A.

    1994-01-01

    A high capacity, long cycle life positive electrode for use in an alkaline rechargeable electrochemical cell comprising: a solid solution nickel hydroxide material having a multiphase structure that comprises at least one polycrystalline .gamma.-phase including a polycrystalline .gamma.-phase unit cell comprising spacedly disposed plates with at least one chemical modifier incorporated around the plates, the plates having a range of stable intersheet distances corresponding to a 2.sup.+ oxidation state and a 3.5.sup.+, or greater, oxidation state; and at least one compositional modifier incorporated into the solid solution nickel hydroxide material to promote the multiphase structure.

  18. Manganese hexacyanomanganate open framework as a high-capacity positive electrode material for sodium-ion batteries

    NASA Astrophysics Data System (ADS)

    Lee, Hyun-Wook; Wang, Richard Y.; Pasta, Mauro; Woo Lee, Seok; Liu, Nian; Cui, Yi

    2014-10-01

    Potential applications of sodium-ion batteries in grid-scale energy storage, portable electronics and electric vehicles have revitalized research interest in these batteries. However, the performance of sodium-ion electrode materials has not been competitive with that of lithium-ion electrode materials. Here we present sodium manganese hexacyanomanganate (Na2MnII[MnII(CN)6]), an open-framework crystal structure material, as a viable positive electrode for sodium-ion batteries. We demonstrate a high discharge capacity of 209 mAh g-1 at C/5 (40 mA g-1) and excellent capacity retention at high rates in a propylene carbonate electrolyte. We provide chemical and structural evidence for the unprecedented storage of 50% more sodium cations than previously thought possible during electrochemical cycling. These results represent a step forward in the development of sodium-ion batteries.

  19. Manganese hexacyanomanganate open framework as a high-capacity positive electrode material for sodium-ion batteries.

    PubMed

    Lee, Hyun-Wook; Wang, Richard Y; Pasta, Mauro; Woo Lee, Seok; Liu, Nian; Cui, Yi

    2014-01-01

    Potential applications of sodium-ion batteries in grid-scale energy storage, portable electronics and electric vehicles have revitalized research interest in these batteries. However, the performance of sodium-ion electrode materials has not been competitive with that of lithium-ion electrode materials. Here we present sodium manganese hexacyanomanganate (Na2MnII[MnII(CN)6]), an open-framework crystal structure material, as a viable positive electrode for sodium-ion batteries. We demonstrate a high discharge capacity of 209 mAh g(-1) at C/5 (40 mA g(-1)) and excellent capacity retention at high rates in a propylene carbonate electrolyte. We provide chemical and structural evidence for the unprecedented storage of 50% more sodium cations than previously thought possible during electrochemical cycling. These results represent a step forward in the development of sodium-ion batteries. PMID:25311066

  20. Study of nickel hydroxide electrodes. 2: Oxidation products of nickel (2) hydroxides

    NASA Technical Reports Server (NTRS)

    Bode, H.; Demelt, K.; White, J.

    1986-01-01

    Pure phases of some oxidized Ni oxides were prepared galvanimetrically with the Ni(2) hydroxide electrode of an alkaline battery. The crystallographic data of these phases, their chemical behavior, and conditions of transition were studied.

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

    NASA Astrophysics Data System (ADS)

    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.

  2. Nickel-cadmium batteries: effect of electrode phase composition on acid leaching process.

    PubMed

    Nogueira, C A; Margarido, F

    2012-01-01

    At the end of their life, Ni-Cd batteries cause a number of environmental problems because of the heavy metals they contain. Because of this, recycling of Ni-Cd batteries has been carried out by dedicated companies using, normally, pyrometallurgical technologies. As an alternative, hydrometallurgical processes have been developed based on leaching operations using several types of leachants. The effect of factors like temperature, acid concentration, reaction time, stirring speed and grinding of material on the leaching yields of metals contained in anodic and cathodic materials (nickel, cadmium and cobalt) using sulphuric acid, is herein explained based on the structural composition of the electrode materials. The nickel, cobalt and cadmium hydroxide phases, even with a small reaction time (less than 15 minutes) and low temperature (50 degrees C) and acid concentration (1.1 M H2SO4), were efficiently leached. However, leaching of the nickel metallic phase was more difficult, requiring higher values of temperature, acid concentration and reaction time (e.g. 85 degrees C, 1.1 M H2SO4 and 5 h, respectively) in order to obtain a good leaching efficiency for anodic and cathodic materials (70% and 93% respectively). The stirring speed was not significant, whereas the grinding of electrode materials seems to promote the compaction of particles, which appears to be critical in the leaching of Ni degrees. These results allowed the identification and understanding of the relationship between the structural composition of electrode materials and the most important factors that affect the H2SO4 leaching of spent Ni-Cd battery electrodes, in order to obtain better metal-recovery efficiency. PMID:22519122

  3. Influence of the active mass particle suspension in electrolyte upon corrosion of negative electrode of a lead-acid battery

    NASA Astrophysics Data System (ADS)

    Kamenev, Yu.; Shtompel, G.; Ostapenko, E.; Leonov, V.

    2014-07-01

    The influence of the suspension of positive active mass particles in the electrolyte on the performance of the negative electrode in a lead-acid battery is studied. A significant increase in the rate of corrosion of the lead electrode is shown when slime particles get in contact with its surface, which may result in the rise of macro-defects on the lugs of the negative electrodes.

  4. Rechargeable Lithium-Air Batteries: Development of Ultra High Specific Energy Rechargeable Lithium-Air Batteries Based on Protected Lithium Metal Electrodes

    SciTech Connect

    2010-07-01

    BEEST Project: PolyPlus is developing the world’s first commercially available rechargeable lithium-air (Li-Air) battery. Li-Air batteries are better than the Li-Ion batteries used in most EVs today because they breathe in air from the atmosphere for use as an active material in the battery, which greatly decreases its weight. Li-Air batteries also store nearly 700% as much energy as traditional Li-Ion batteries. A lighter battery would improve the range of EVs dramatically. Polyplus is on track to making a critical breakthrough: the first manufacturable protective membrane between its lithium–based negative electrode and the reaction chamber where it reacts with oxygen from the air. This gives the battery the unique ability to recharge by moving lithium in and out of the battery’s reaction chamber for storage until the battery needs to discharge once again. Until now, engineers had been unable to create the complex packaging and air-breathing components required to turn Li-Air batteries into rechargeable systems.

  5. Ethanol oxidation on Pt single-crystal electrodes: surface-structure effects in alkaline medium.

    PubMed

    Busó-Rogero, Carlos; Herrero, Enrique; Feliu, Juan M

    2014-07-21

    Ethanol oxidation in 0.1 M NaOH on single-crystal electrodes has been studied using electrochemical and FTIR techniques. The results show that the activity order is the opposite of that found in acidic solutions. The Pt(111) electrode displays the highest currents and also the highest onset potential of all the electrodes. The onset potential for the oxidation of ethanol is linked to the adsorption of OH on the electrode surface. However, small (or even negligible) amounts of CO(ads) and carbonate are detected by FTIR, which implies that cleavage of the C-C bond is not favored in this medium. The activity of the electrodes diminishes quickly upon cycling. The diminution of the activity is proportional to the measured currents and is linked to the formation and polymerization of acetaldehyde, which adsorbs onto the electrode surface and prevents further oxidation. PMID:24782218

  6. Reductive atmospheric acid leaching of spent alkaline batteries in H2SO4/Na2SO3 solutions

    NASA Astrophysics Data System (ADS)

    Morcali, Mehmet Hakan

    2015-07-01

    This work studies the optimum reductive leaching process for manganese and zinc recovery from spent alkaline battery paste. The effects of reducing agents, acid concentration, pulp density, reaction temperature, and leaching time on the dissolution of manganese and zinc were investigated in detail. Manganese dissolution by reductive acidic media is an intermediate-controlled process with an activation energy of 12.28 kJ·mol-1. After being leached, manganese and zinc were selectively precipitated with sodium hydroxide. The zinc was entirely converted into zincate (Zn(OH){4/2-}) ions and thus did not co-precipitate with manganese hydroxide during this treatment (2.0 M NaOH, 90 min, 200 r/min, pH > 13). After the manganese was removed from the solution, the Zn(OH){4/2-} was precipitated as zinc sulfate in the presence of sulfuric acid. The results indicated that this process could be effective in recovering manganese and zinc from alkaline batteries.

  7. Negligible "negative space-charge layer effects" at oxide-electrolyte/electrode interfaces of thin-film batteries.

    PubMed

    Haruta, Masakazu; Shiraki, Susumu; Suzuki, Tohru; Kumatani, Akichika; Ohsawa, Takeo; Takagi, Yoshitaka; Shimizu, Ryota; Hitosugi, Taro

    2015-03-11

    In this paper, we report the surprisingly low electrolyte/electrode interface resistance of 8.6 Ω cm(2) observed in thin-film batteries. This value is an order of magnitude smaller than that presented in previous reports on all-solid-state lithium batteries. The value is also smaller than that found in a liquid electrolyte-based batteries. The low interface resistance indicates that the negative space-charge layer effects at the Li3PO(4-x)N(x)/LiCoO2 interface are negligible and demonstrates that it is possible to fabricate all-solid state batteries with faster charging/discharging properties. PMID:25710500

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

    SciTech Connect

    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.

  9. In situ investigation of working battery electrodes using synchrotron x-ray diffraction

    SciTech Connect

    Jisrawi, N.M.; Thurston, T.R.; Yang, X.Q.

    1996-12-31

    The results of an in situ investigation of the structural changes that occur during the operation of working battery electrodes using synchrotron radiation are presented. Two types of electrodes were investigated: an AB{sub 2}-type Laves phase alloy anode with the composition Zr{sub x}Ti{sub 1-x}M{sub 2} and a proprietary cell based on a Li{sub x}Mn{sub 2}O{sub 4} spinel compound cathode made by Gould electronics. For the Laves phase alloy compositions with x=0.25 and 0.5 and M=V{sub 0.5}N{sub 1.1}Mn{sub 0.2}Fe{sub 0.2} were examined. Cells made from two different batches of Li{sub x}Mn{sub 2}O{sub 4} material were investigated. The relationships between battery performance and structural changes will be discussed. In the later case, we also discuss the role of over-discharging on the Li{sub x}Mn{sub 2}O{sub 4} structure and on battery operation.

  10. Performance improvements of alkaline batteries by studying the effects of different kinds of surfactant and different derivatives of benzene on the electrochemical properties of electrolytic zinc

    NASA Astrophysics Data System (ADS)

    Ghavami, Robab Khayat; Rafiei, Zahra

    Electrolytic zinc powders were prepared in 12 M KOH, 4 wt.% zinc oxide solutions in the presence of different kinds of surfactant and organic additives using the galvanostatic technique. Then the electrochemical behavior of zinc was investigated using the sweep voltametry technique. Zinc samples electrolyzed in the presence of cationic cetyl trimethyl ammonium bromide (Zn-CTAB), have maximum corrosion rate. Furthermore, scanning electron microscopy revealed the highest surface area. Zinc deposited with anionic surfactants, sodium dodecyl benzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS), have high dendritic and secondary growth. More zinc ions electrolyzed on the cathode electrode in the presence of SDBS compared with SDS. We suppose the Benzene molecule in SDBS changes morphology, thus effects of the benzene molecule is investigated by utilizing several organic compounds during zinc electrodeposition. Naphthalene with 10 pi electrons at two fused rings decreases corrosion rate and needle growth of zinc deposited, compared to benzyl chloride which has 6 pi electrons. Enhanced delocalization of pi electrons by strongly activating group (-NH 2) in the aniline molecule increases the corrosion rate and dendrites compared with benzyl chloride, which has the weakly activating group (-CH 2Cl). The addition of chloro benzene with inactivating and electrodrawing group (-Cl) creates high surface area without any dendritic growth. The effects of electrolyte additives on the electrochemical capacity of AA-sized alkaline Zn-MnO 2 batteries are verified. The addition of Triton X-100 in anode gel resulted in maximum electrical capacity. Anionic (SDBS and SDS) additives gave higher electrical capacity than cationic (CTAB). Also, the reaction mechanism for zinc electrodeposition in alkaline electrolytes and its dependence upon the presence of organic additives are discussed in detail.

  11. Three-dimensional nanoporous gold-cobalt oxide electrode for high-performance electroreduction of hydrogen peroxide in alkaline medium

    NASA Astrophysics Data System (ADS)

    Li, Zhihao; He, Yanghua; Ke, Xi; Gan, Lin; Zhao, Jie; Cui, Guofeng; Wu, Gang

    2015-10-01

    Using a simple hydrothermal method combined with a post-annealing treatment, cobalt oxide (Co3O4) nanosheet arrays are grown on three-dimensional (3D) nanoporous gold (NPG) film supported on Ni foam substrates, in which NPG is fabricated by chemically dealloying electrodeposited Au-Sn alloy films. The morphology and structure of the Co3O4@NPG/Ni foam hybrids are characterized by scanning electron microscopy (SEM) and X-ray diffraction (XRD). The electrochemical activity of the Co3O4@NPG/Ni foam electrode toward hydrogen peroxide electroreduction in alkaline medium is studied by cyclic voltammetry (CV), linear sweep voltammetry (LSV), and chronoamperometry (CA). The results demonstrate that the Co3O4@NPG/Ni foam electrode possesses exceptionally high catalytic activity and excellent stability for the peroxide electroreduction, resulting mainly from the unique electrode architecture. The combined 3D hierarchical porous structures of NPG/Ni foam with the open and porous structures of Co3O4 nanosheet arrays facilitate the mass transport and charge transfer. Therefore, the metal oxides supported on 3D hierarchical porous NPG/Ni foam framework may hold great promise to be effective electrodes for electrocatalytic reduction of peroxide and other electrochemical reactions.

  12. Reduced order modeling of mechanical degradation induced performance decay in lithium-ion battery porous electrodes

    DOE PAGESBeta

    Barai, Pallab; Smith, Kandler; Chen, Chien -Fan; Kim, Gi -Heon; Mukherjee, Partha P.

    2015-06-17

    In this paper, a one-dimensional computational framework is developed that can solve for the evolution of voltage and current in a lithium-ion battery electrode under different operating conditions. A reduced order model is specifically constructed to predict the growth of mechanical degradation within the active particles of the carbon anode as a function of particle size and C-rate. Using an effective diffusivity relation, the impact of microcracks on the diffusivity of the active particles has been captured. Reduction in capacity due to formation of microcracks within the negative electrode under different operating conditions (constant current discharge and constant current constantmore » voltage charge) has been investigated. At the beginning of constant current discharge, mechanical damage to electrode particles predominantly occurs near the separator. As the reaction front shifts, mechanical damage spreads across the thickness of the negative electrode and becomes relatively uniform under multiple discharge/charge cycles. Mechanical degradation under different drive cycle conditions has been explored. It is observed that electrodes with larger particle sizes are prone to capacity fade due to microcrack formation. Finally, under drive cycle conditions, small particles close to the separator and large particles close to the current collector can help in reducing the capacity fade due to mechanical degradation.« less

  13. Reduced order modeling of mechanical degradation induced performance decay in lithium-ion battery porous electrodes

    SciTech Connect

    Barai, Pallab; Smith, Kandler; Chen, Chien -Fan; Kim, Gi -Heon; Mukherjee, Partha P.

    2015-06-17

    In this paper, a one-dimensional computational framework is developed that can solve for the evolution of voltage and current in a lithium-ion battery electrode under different operating conditions. A reduced order model is specifically constructed to predict the growth of mechanical degradation within the active particles of the carbon anode as a function of particle size and C-rate. Using an effective diffusivity relation, the impact of microcracks on the diffusivity of the active particles has been captured. Reduction in capacity due to formation of microcracks within the negative electrode under different operating conditions (constant current discharge and constant current constant voltage charge) has been investigated. At the beginning of constant current discharge, mechanical damage to electrode particles predominantly occurs near the separator. As the reaction front shifts, mechanical damage spreads across the thickness of the negative electrode and becomes relatively uniform under multiple discharge/charge cycles. Mechanical degradation under different drive cycle conditions has been explored. It is observed that electrodes with larger particle sizes are prone to capacity fade due to microcrack formation. Finally, under drive cycle conditions, small particles close to the separator and large particles close to the current collector can help in reducing the capacity fade due to mechanical degradation.

  14. Dry spun 3D woven carbon nanotube anode electrode for Li-lon batteries.

    PubMed

    Ryu, Seongwoo; Kim, Yunkyoung; Lee, Haeshin; Hong, Soon Hyung

    2014-12-01

    Although carbon nanotubes (CNTs) have extraordinary mechanical, thermal, and electrical properties, application of CNTs remains limited due to their unique nano-sized tubular forms. CNT electrodes have relatively high sheet resistance, which does not meet the industrial requirements of various electrode materials. Thus, there are still challenges for improving the performance of CNTs in real applications, particularly in terms of satisfying industrial requirements. In this study, to utilize CNTs in bulk scale electrode applications, we developed a dry spinning technique. The dry spinning technique is a solid state fiber spinning technique that provides an adjustable aligned structure. The dry spinning approach also offers a facile and inexpensive fabrication process, factors which are favorable for industrial scalability for fabricating electrodes. We demonstrate a multilayer stacking process for enhancing the performance for Li-ion batteries. Multi-layer CNT textiles have low sheet resistance and a 3D woven structure provides high surface area. The fabricated 3D woven structured electrode delivers a higher reversible capacity of more than 400 mA hr/g with high cycle stabilities. PMID:25971028

  15. Dispersion of Nanocrystalline Fe3O4 within Composite Electrodes: Insights on Battery-Related Electrochemistry.

    PubMed

    Bock, David C; Pelliccione, Christopher J; Zhang, Wei; Wang, Jiajun; Knehr, K W; Wang, Jun; Wang, Feng; West, Alan C; Marschilok, Amy C; Takeuchi, Kenneth J; Takeuchi, Esther S

    2016-05-11

    Aggregation of nanosized materials in composite lithium-ion-battery electrodes can be a significant factor influencing electrochemical behavior. In this study, aggregation was controlled in magnetite, Fe3O4, composite electrodes via oleic acid capping and subsequent dispersion in a carbon black matrix. A heat treatment process was effective in the removal of the oleic acid capping agent while preserving a high degree of Fe3O4 dispersion. Electrochemical testing showed that Fe3O4 dispersion is initially beneficial in delivering a higher functional capacity, in agreement with continuum model simulations. However, increased capacity fade upon extended cycling was observed for the dispersed Fe3O4 composites relative to the aggregated Fe3O4 composites. X-ray absorption spectroscopy measurements of electrodes post cycling indicated that the dispersed Fe3O4 electrodes are more oxidized in the discharged state, consistent with reduced reversibility compared with the aggregated sample. Higher charge-transfer resistance for the dispersed sample after cycling suggests increased surface-film formation on the dispersed, high-surface-area nanocrystalline Fe3O4 compared to the aggregated materials. This study provides insight into the specific effects of aggregation on electrochemistry through a multiscale view of mechanisms for magnetite composite electrodes. PMID:27096464

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

    NASA Astrophysics Data System (ADS)

    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. Raman diagnostics of LiCoO2 electrodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Gross, Toni; Hess, Christian

    2014-06-01

    LiCoO2 based electrode materials were characterized in detail using visible Raman spectroscopy. The studied materials comprise the active LiCoO2 material itself as well as electrochemically relevant composites of LiCoO2 with binder and conductive additives. Spatially resolved analysis, i.e. mapping of LiCoO2 composite electrodes reveals a significant variation of chemical composition across the electrode surface. Based on wavelength-dependent studies we demonstrate the presence of a resonance enhancement for LiCoO2 materials for green laser excitation allowing for in situ studies on the LiCoO2-based electrodes during lithium de-intercalation. During in situ experiments no significant structural changes occur consistent with the fact that visible Raman spectroscopy probes mainly the surface region of the LiCoO2 composite electrode. Our results demonstrate the potential of Raman spectroscopy for spatially resolved and in situ analysis of lithium-ion batteries.

  18. Electrochemical properties of monolithic nickel sulfide electrodes for use in sodium batteries

    SciTech Connect

    Go, Dae-Yeon; Park, Jinsoo; Noh, Pan-Jin; Cho, Gyu-Bong; Ryu, Ho-Suk; Nam, Tae-Hyeon; Ahn, Hyo-Jun; Kim, Ki-Won

    2014-10-15

    Highlights: • We succeeded in preparing monolithic Ni{sub 3}S{sub 2} integrated electrode through the sulfuration. • The sulfuration is a facile and useful method to synthesize metal sulfides with nanostructure. • As-prepared monolithic Ni{sub 3}S{sub 2} electrodes showed very stable and cycle performance over charge/discharge cycling. - Abstract: Monolithic nickel sulfide electrodes were prepared using a facile synthesis method, sulfuration and annealing. As-prepared Ni{sub 3}S{sub 2} electrodes were characterized by X-ray diffractometry and field emission scanning electron microscopy. Thermal stability was determined by thermal gravimetric analysis and differential scanning calorimetry. Electrochemical properties were measured by galvanostatic charge and discharge cycling for Na-ion batteries. Three kinds of Ni{sub 3}S{sub 2} electrodes were prepared by varying the sulfuration time (5, 15 and 25 min). The electrochemical results indicated that the capacities increased with an increase in sulfuration time and the cycle performance was stable as a result of monolithic integration of nanostructured Ni{sub 3}S{sub 2} on Ni plates, leading to low interfacial resistance.

  19. Electronic Structure at Electrode/Electrolyte Interfaces in Magnesium based Batteries

    NASA Astrophysics Data System (ADS)

    Balachandran, Janakiraman; Siegel, Donald

    2015-03-01

    Magnesium is a promising multivalent element for use in next generation electrochemical energy storage systems. However, a wide range of challenges such as low coulombic efficiency, low/varying capacity and cyclability need to be resolved in order to realize Mg based batteries. Many of these issues can be related to interfacial phenomena between the Mg anode and common electrolytes. Ab-initio based computational models of these interfaces can provide insights on the interfacial interactions that can be difficult to probe experimentally. In this work we present ab-initio computations of common electrolyte solvents (THF, DME) in contact with two model electrode surfaces namely -- (i) an ``SEI-free'' electrode based on Mg metal and, (ii) a ``passivated'' electrode consisting of MgO. We perform GW calculations to predict the reorganization of the molecular orbitals (HOMO/LUMO) upon contact with the these surfaces and their alignment with respect to the Fermi energy of the electrodes. These computations are in turn compared with more efficient GGA (PBE) & Hybrid (HSE) functional calculations. The results obtained from these computations enable us to qualitatively describe the stability of these solvent molecules at electrode-electrolyte interfaces

  20. Direct synthesis and coating of advanced nanocomposite negative electrodes for Li-ion batteries via electrospraying

    NASA Astrophysics Data System (ADS)

    Valvo, M.; García-Tamayo, E.; Lafont, U.; Kelder, E. M.

    A direct approach for the synthesis and coating of advanced nanocomposite negative electrodes via a single-step process at low temperature is presented. Metal-oxide/PVdF nanocomposites are obtained in one step by electrospray pyrolysis of precursor solutions containing dissolved metal salts together with polyvinylidene fluoride (PVdF) as binder. In this way, small oxide nanoparticles are generated and dispersed in situ in the binder creating nanocomposite structures, while being coated at once as thin electrode layers on stainless steel coin cell cans. The intimate contact between the nanoparticles and the binder favours enhanced adhesion of the materials in the overall electrode structure and adequate electrochemical performances are obtained without any conductive additive. Three nanocomposite oxide/PVdF materials (i.e. SnO 2, CoO and Fe 2O 3) are reported here as preliminary examples of negative electrodes. The results show that this approach is suitable, not only for the fabrication of nanocomposite electrodes for Li-ion batteries, but also for other novel applications.

  1. Dispersion of nanocrystalline Fe3O4 within composite electrodes: Insights on battery-related electrochemistry

    DOE PAGESBeta

    David C. Bock; Takeuchi, Kenneth J.; Pelliccione, Christopher J.; Zhang, Wei; Wang, Jiajun; Knehr, K. W.; Wang, Jun; Wang, Feng; West, Alan C.; Marschilok, Amy C.; et al

    2016-04-20

    Aggregation of nanosized materials in composite lithium-ion-battery electrodes can be a significant factor influencing electrochemical behavior. In this study, aggregation was controlled in magnetite, Fe3O4, composite electrodes via oleic acid capping and subsequent dispersion in a carbon black matrix. A heat treatment process was effective in the removal of the oleic acid capping agent while preserving a high degree of Fe3O4 dispersion. Electrochemical testing showed that Fe3O4 dispersion is initially beneficial in delivering a higher functional capacity, in agreement with continuum model simulations. However, increased capacity fade upon extended cycling was observed for the dispersed Fe3O4 composites relative to themore » aggregated Fe3O4 composites. X-ray absorption spectroscopy measurements of electrodes post cycling indicated that the dispersed Fe3O4 electrodes are more oxidized in the discharged state, consistent with reduced reversibility compared with the aggregated sample. Higher charge-transfer resistance for the dispersed sample after cycling suggests increased surface-film formation on the dispersed, high-surface-area nanocrystalline Fe3O4 compared to the aggregated materials. Furthermore, this study provides insight into the specific effects of aggregation on electrochemistry through a multiscale view of mechanisms for magnetite composite electrodes.« less

  2. Electrode-electrolyte interface in Li-ion batteries: current understanding and new insights.

    PubMed

    Gauthier, Magali; Carney, Thomas J; Grimaud, Alexis; Giordano, Livia; Pour, Nir; Chang, Hao-Hsun; Fenning, David P; Lux, Simon F; Paschos, Odysseas; Bauer, Christoph; Maglia, Filippo; Lupart, Saskia; Lamp, Peter; Shao-Horn, Yang

    2015-11-19

    Understanding reactions at the electrode/electrolyte interface (EEI) is essential to developing strategies to enhance cycle life and safety of lithium batteries. Despite research in the past four decades, there is still limited understanding by what means different components are formed at the EEI and how they influence EEI layer properties. We review findings used to establish the well-known mosaic structure model for the EEI (often referred to as solid electrolyte interphase or SEI) on negative electrodes including lithium, graphite, tin, and silicon. Much less understanding exists for EEI layers for positive electrodes. High-capacity Li-rich layered oxides yLi2-xMnO3·(1-y)Li1-xMO2, which can generate highly reactive species toward the electrolyte via oxygen anion redox, highlight the critical need to understand reactions with the electrolyte and EEI layers for advanced positive electrodes. Recent advances in in situ characterization of well-defined electrode surfaces can provide mechanistic insights and strategies to tailor EEI layer composition and properties. PMID:26510477

  3. Bipolar battery

    DOEpatents

    Kaun, Thomas D.

    1992-01-01

    A bipolar battery having a plurality of cells. The bipolar battery includes: a negative electrode; a positive electrode and a separator element disposed between the negative electrode and the positive electrode, the separator element electrically insulating the electrodes from one another; an electrolyte disposed within at least one of the negative electrode, the positive electrode and the separator element; and an electrode containment structure including a cup-like electrode holder.

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Designing an elastomeric binder for large-volume-change electrodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Chen, Zonghai

    It is of commercial importance to develop high capacity negative and positive electrode materials for lithium-ion batteries to meet the energy requirements of portable electronic devices. Excellent capacity retention has been achieved for thin sputtered films of amorphous Si, Ge and Si-Sn alloys even when cycled to 2000 mAh/g and above, which suggests that amorphous alloys are capable of extended cycling. However, PVDF-based composite electrodes incorporating a-Si0.64Sn0.36/Ag powder (10 wt% silver coating) (˜10mum) still suffer from severe capacity fading because of the huge volumetric changes of a-Si0.64Sn0.36/Ag during charge/discharge cycling. It is the objective of this thesis to understand the problem scientifically and to propose practical solutions to solve this problem. Mechanical studies of binders for lithium battery electrodes have never been reported in the literature. The mechanical properties of commonly used binders, such as poly(vinylidene fluoride) (PVDF), haven't been challenged because commercially used active materials, such as LiCoO2 and graphite, have small volumetric changes (<10%) during charge/discharge cycling. However, the recently proposed metallic alloys have huge volumetric changes (up to 250%) during cycling. In this case, the mechanical properties of the binder become critical. A tether model is proposed to qualitatively understand the capacity fading of high-volume-change electrodes, and to predict the properties of a good binder system. A crosslinking/coupling route was used to modify the binder system according to the requirements of the tether model. A poly(vinylidene fluoride-tetrafluoroethylenepropylene)-based elastomeric binder system was designed to successfully improve the capacity retention of a-Si0.64 Sn0.36/Ag composite electrodes. In this thesis, it has also proven nontrivial to maximize the capacity retention of large-volume-change electrodes even when a fixed elastomeric binder system was used. The parameters that

  7. Rechargeable zinc cell with alkaline electrolyte which inhibits shape change in zinc electrode

    DOEpatents

    Adler, Thomas C.; McLarnon, Frank R.; Cairns, Elton J.

    1995-01-01

    An improved rechargeable zinc cell is described comprising a zinc electrode and another electrode such as, for example, a nickel-containing electrode, and having an electrolyte containing one or more hydroxides having the formula M(OH), one or more fluorides having the formula MF, and one or more carbonates having the formula M.sub.2 CO.sub.3, where M is a metal selected from the group consisting of alkali metals. The electrolyte inhibits shape change in the zinc electrode, i.e., the zinc electrode exhibits low shape change, resulting in an improved capacity retention of the cell over an number of charge-discharge cycles, while still maintaining high discharge rate characteristics.

  8. High performance nano-Ni/Graphite electrode for electro-oxidation in direct alkaline ethanol fuel cells

    NASA Astrophysics Data System (ADS)

    Soliman, Ahmed B.; Abdel-Samad, Hesham S.; Abdel Rehim, Sayed S.; Ahmed, Mohamed A.; Hassan, Hamdy H.

    2016-09-01

    Ni/Graphite electrocatalysts (Ni/G) are successfully prepared through electrodeposition of Ni from acidic (pH = 0.8) and feebly acidic (pH = 5.5) aqueous Ni (II) baths. The efficiencies of such electrodes are investigated as anodes for direct alkaline ethanol fuel cells through their ethanol electrooxidation cyclic voltammetric (CV) response in alkaline medium. A direct proportionality between the amount of the electrodeposited Ni and its CV response is found. The amounts of the deposited Ni from the two baths are recorded using the Electrochemical Quartz Crystal Microbalance (eQCM). The Ni/G electrodes prepared from the feebly acidic bath show a higher electrocatalytic response than those prepared from the acidic bath. Surface morphology of the Ni particles electrodeposited from feebly acidic bath appears in a nano-scale dimension. Various electrochemical experiments are conducted to confirm that the Ni/G ethanol electrooxidation CV response greatly depends on the pH rather than nickel ion concentration of the deposition bath. The eQCM technique is used to detect the crystalline phases of nickel as α-Ni(OH)2/γ-NiOOH and β-Ni(OH)2/β-NiOOH and their in-situ inter-transformations during the potentiodynamic polarization.

  9. Composition and crystal structure of perovskite films attained from electrodes of used car battery

    NASA Astrophysics Data System (ADS)

    Dhiaputra, Ilham; Permana, Bayu; Maulana, Yusep; Inayatie, Yuniar Dwi; Purba, Yonatan R.; Bahtiar, Ayi

    2016-02-01

    Perovskite solar cells have been intensively investigated for high performance and low-cost solid-state solar cells. Perovskite based-lead materials are commonly used as active material for high power conversion efficiency solar cells. Herein, we report our study on the development of used electrodes car battery as a cheap raw lead material to be converted into lead (II) iodide PbI2 by using simple chemical method. We have successfully obtained PbI2 material with purity higher than 85% and its crystal structure is comparable with that of commercial product. The perovskite CH3NH3PbI3 film was prepared by spin-coating of PbI2 solution and followed by spin-coating two-times of methylamonium iodide (MAI) solution. In this paper, the crystal structure of perovskite film attained from used car battery is shown and compared with that of prepared from commercial PbI2. By utilizing the used car battery into perovskite valuable material for high performance solar cells, we can not only improve the economical value (added-value) of wasted car battery but also we can simultaneously save the environment.

  10. Performance of 2,4-dinitrophenol as a positive electrode in magnesium reserve batteries

    NASA Astrophysics Data System (ADS)

    Gopukumar, S.; Natarajan, S.; Thirunakaran, R.; Sakthivel, M.

    Magnesium is an interesting anode battery material with many advantages such as its high standard potential of (-2.37 V), low cost and good low-temperature performance due to an exothermic corrosion reaction during discharge. Organic aromatic nitro compounds undergo multi-electron transfers of up to 18 during discharge, and hence, give high specific energies (up to 2 A h/g) in comparison with conventional inorganic battery depolarizers such as MnO 2, HgO, CuO and AgO. Thus, it is worthwhile fabricating and studying the performance of a battery system combining magnesium and 2,4-dinitrophenol (DNP) using aqueous halide electrolytes like MgCl 2, MgBr 2 and Mg(ClO 4) 2.This paper describes the preparation of DNP cathodes after standardization of the cathode mixture. Mg/DNP cells (1 V, 1 A h) have been assembled using the above cathode in conjunction with magnesium alloy (AZ 31) anodes and discharged at different current densities (1.7, 3.3, 5, 6.6 mA/cm 2) in 2 M MgCl 2, MgBr 2 and Mg(Cl0 4) 2. Cyclic voltammograms of DNP have been recorded in 2 M Mg(ClO 4) 2 at various sweep rates and concentrations in order to understand the reduction behavior. The study suggests that DNP is a suitable organic compound for use as a positive electrode material in magnesium reserve batteries.

  11. A High-Performance Rechargeable Iron Electrode for Large-Scale Battery-Based Energy Storage

    SciTech Connect

    Manohar, AK; Malkhandi, S; Yang, B; Yang, C; Prakash, GKS; Narayanan, SR

    2012-01-01

    Inexpensive, robust and efficient large-scale electrical energy storage systems are vital to the utilization of electricity generated from solar and wind resources. In this regard, the low cost, robustness, and eco-friendliness of aqueous iron-based rechargeable batteries are particularly attractive and compelling. However, wasteful evolution of hydrogen during charging and the inability to discharge at high rates have limited the deployment of iron-based aqueous batteries. We report here new chemical formulations of the rechargeable iron battery electrode to achieve a ten-fold reduction in the hydrogen evolution rate, an unprecedented charging efficiency of 96%, a high specific capacity of 0.3 Ah/g, and a twenty-fold increase in discharge rate capability. We show that modifying high-purity carbonyl iron by in situ electro-deposition of bismuth leads to substantial inhibition of the kinetics of the hydrogen evolution reaction. The in situ formation of conductive iron sulfides mitigates the passivation by iron hydroxide thereby allowing high discharge rates and high specific capacity to be simultaneously achieved. These major performance improvements are crucial to advancing the prospect of a sustainable large-scale energy storage solution based on aqueous iron-based rechargeable batteries. (C) 2012 The Electrochemical Society. [DOI: 10.1149/2.034208jes] All rights reserved.

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

    NASA Astrophysics Data System (ADS)

    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.

  13. Lithium Batteries: Carbon-Rich Active Materials with Macrocyclic Nanochannels for High-Capacity Negative Electrodes in All-Solid-State Lithium Rechargeable Batteries (Small 25/2016).

    PubMed

    Sato, Sota; Unemoto, Atsushi; Ikeda, Takuji; Orimo, Shin-Ichi; Isobe, Hiroyuki

    2016-07-01

    On page 3381, S. Sato, S. Orimo, H. Isobe, and co-workers present the first macrocyclic material to be utilized in negative electrodes of all-solid-state, rechargeable lithium batteries. Assembled to align the molecular openings, the macrocycle paves paths for lithium to migrate to the π-stack intercalation sites for the storage. The macrocyclic nanochannel of a nanometer-scale diameter further provides extra spaces for the lithium storage to surpass conventional graphitic electrodes in the capacity. PMID:27364310

  14. Unraveling the storage mechanism in organic carbonyl electrodes for sodium-ion batteries

    PubMed Central

    Wu, Xiaoyan; Jin, Shifeng; Zhang, Zhizhen; Jiang, Liwei; Mu, Linqin; Hu, Yong-Sheng; Li, Hong; Chen, Xiaolong; Armand, Michel; Chen, Liquan; Huang, Xuejie

    2015-01-01

    Organic carbonyl compounds represent a promising class of electrode materials for secondary batteries; however, the storage mechanism still remains unclear. We take Na2C6H2O4 as an example to unravel the mechanism. It consists of alternating Na-O octahedral inorganic layer and π-stacked benzene organic layer in spatial separation, delivering a high reversible capacity and first coulombic efficiency. The experiment and calculation results reveal that the Na-O inorganic layer provides both Na+ ion transport pathway and storage site, whereas the benzene organic layer provides electron transport pathway and redox center. Our contribution provides a brand-new insight in understanding the storage mechanism in inorganic-organic layered host and opens up a new exciting direction for designing new materials for secondary batteries. PMID:26601260

  15. Cubic KTi2(PO4)3 as electrode materials for sodium-ion batteries.

    PubMed

    Han, Jin; Xu, Maowen; Niu, Yubin; Jia, Min; Liu, Ting; Li, Chang Ming

    2016-12-01

    A novel cubic KTi2(PO4)3 is successfully synthesized via a facile hydrothermal method combined with a subsequent annealing treatment and further used as electrode material for sodium-ion batteries for the first time. For comparison, carbon-coated KTi2(PO4)3 obtained by a normal cane sugar-assisted method reveals superior electrochemical performances in sodium-ion battery. Besides of the high coulombic efficiency of nearly 100% after 100 cycles, a stable capacity of 112mAhg(-1) can be achieved at 0.5C after 100 cycles, and still maintains to 105mAhg(-1) after 500 cycles with capacity retention of approximately 90%. PMID:27552414

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

    PubMed Central

    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. PMID:23233879

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

    NASA Astrophysics Data System (ADS)

    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.

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

    PubMed Central

    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.

    2016-01-01

    Summary 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. PMID:26999804

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

    PubMed

    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. PMID:26999804

  20. The structural and electrochemical dynamics of the electrode-electrolyte interphase of metal fluoride nanocomposite positive electrodes for lithium batteries

    NASA Astrophysics Data System (ADS)

    Gmitter, Andrew John

    Metal fluorides are attractive for use as positive electrodes in Li and Li-ion batteries because of their high gravimetric and volumetric energy densities. When synthesized into nanocomposites, these materials undergo conversion reactions and exhibit near theoretical specific capacity and good rate capability. Despite these positive attributes, metal fluorides nanocomposites generally exhibit unacceptable rates of capacity loss during cycling. This stands as a significant barrier to their realization as a viable battery technology. This thesis explored a candidate material, BiF3, and for the first time, the mechanisms by which metal fluoride nanocomposite positive electrode materials fail during cycling have been investigated. The chemistry of the electrode / electrolyte interface and its influence on the BiF3 material were of greatest interest. Early in the course of study, it was discovered that the Bi0 metal produced through the discharge reaction of BiF3 was a catalytically active site for the electrochemical reduction of ethylene carbonate (EC) at potentials exceeding 2 V vs. Li/Li+. This potential range is well above the values typically observed on carbonaceous negative electrodes on which preferential reduction of electrolyte species yields insoluble phases. These ionically conducting layers are deemed solid-electrolyte interphases (SEI), and in the case of carbonaceous materials, they are necessary for enabling functionality of the electrode and preventing deleterious interactions with the electrolyte. Thorough electrochemical and spectroscopic examinations identified Li2CO3 as the predominant SEI species formed on Bi0 from EC. In stark contrast to carbonaceous materials, the presence of SEI on Bi0 was detrimental to the cycling performance of BiF3. Elaboration of this topic identified instability of the SEI during the charging process of the BiF3 and the formation of BiOxF3-2x in the fully charged state. Electrolytes composed of linear

  1. Ag/C nanoparticles as an cathode catalyst for a zinc-air battery with a flowing alkaline electrolyte

    NASA Astrophysics Data System (ADS)

    Han, Jia-Jun; Li, Ning; Zhang, Tian-Yun

    The cyclic voltammetry indicated that the oxygen reduction reaction (ORR) proceeded by the four-electron pathway mechanism on larger Ag particles (174 nm), and that the ORR proceeded by the four-electron pathway and the two-electron pathway mechanisms on finer Ag particles (4.1 nm), simultaneously. The kinetics towards ORR was measured at a rotating disk electrode (RDE) with Ag/C electrode. The number of exchanged electrons for the ORR was found to be close to four on larger Ag particles (174 nm) and close to three on finer Ag particles (4.1 nm). The zinc-air battery with Ag/C catalysts (25.9 nm) was fabricated and examined.

  2. Prismatic sealed nickel-cadmium batteries utilizing fiber structured electrodes. I - New advances in cell design

    NASA Astrophysics Data System (ADS)

    Haschka, Friedrich; Benczur-Urmossy, Gabor; Anderman, Menahem

    Prismatic sealed Ni/Cd cells of fiber structured electrodes offer the potential to fully recharge a battery in a uniquely short time. It was demonstrated that the cells show excellent cycle life. The design is not restricted to 20 Ah rated capacity. Cells of 50 Ah have been built and tested in an electric hybrid vehicle. A specially designed ultra high-power cell of 45 Ah rated capacity for APU cranking in commerical aircraft supplies 50 percent more peak power than vented Ni/Cd sintered plate aircraft cells. The fiber structured sealed FNC-RECOM cell will not require any maintenance.

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

    PubMed

    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. PMID:21574248

  4. Amorphous Vanadium Oxide/Carbon Composite Positive Electrode for Rechargeable Aluminum Battery.

    PubMed

    Chiku, Masanobu; Takeda, Hiroki; Matsumura, Shota; Higuchi, Eiji; Inoue, Hiroshi

    2015-11-11

    Amorphous vanadium oxide/carbon composite (V2O5/C) was first applied to the positive electrode active material for rechargeable aluminum batteries. Electrochemical properties of V2O5/C were investigated by cyclic voltammetry and charge-discharge tests. Reversible reduction/oxidation peaks were observed for the V2O5/C electrode and the rechargeable aluminum cell showed the maximum discharge capacity over 200 mAh g(-1) in the first discharging. The XPS analyses after discharging and the following charging exhibited that the redox of vanadium ion in the V2O5/C active material occurred during discharging and charging, and the average valence of V changed between 4.14 and 4.85. PMID:26489385

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

    NASA Astrophysics Data System (ADS)

    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.

  6. Study of the influence of carbon on the negative lead-acid battery electrodes

    NASA Astrophysics Data System (ADS)

    Bača, Petr; Micka, Karel; Křivík, Petr; Tonar, Karel; Tošer, Pavel

    Experiments were made with negative lead-acid battery electrodes doped with different concentrations of powdered carbon. It turned out that the rate of formation decreased with the rising concentration of carbon added into the active material. During accelerated cycling in the PSoC regime, the cycle life showed a maximum at a concentration of carbon near 1%, whereas at lower or higher concentrations the cycle life was profoundly lower. A marked increase of the active mass resistance with the cycle number was recorded at carbon concentrations above 2%. Orientation experiments showed that compression of the lead-acid laboratory cells caused an increase of the cycle life of the negative electrode in the studied regime.

  7. Controlled electrochemical etching of nanoporous Si anodes and its discharge behavior in alkaline Si-air batteries.

    PubMed

    Park, Dong-Won; Kim, Soeun; Ocon, Joey D; Abrenica, Graniel Harne A; Lee, Jae Kwang; Lee, Jaeyoung

    2015-02-11

    We report the fabrication of nanoporous silicon (nPSi) electrodes via electrochemical etching to form a porous Si layer with controllable thickness and pore size. Varying the etching time and ethanolic HF concentration results in different surface morphologies, with various degrees of electrolyte access depending on the pore characteristics. Optimizing the etching condition leads to well-developed nPSi electrodes, which have thick porous layers and smaller pore diameter and exhibit improved discharge behavior as anodes in alkaline Si-air cells in contrast to flat Si anode. Although electrochemical etching is effective in improving the interfacial characteristics of Si in terms of high surface area, we observed that mild anodization occurs and produces an oxide overlayer. We then show that this oxide layer in nPSi anodes can be effectively removed to produce an nPSi anode with good discharge behavior in an actual alkaline Si-air cell. In the future, the combination of high surface area nPSi anodes with nonaqueous electrolytes (e.g., room-temperature ionic liquid electrolyte) to minimize the strong passivation behavior and self-discharge in Si could lead to Si-air cells with a stable voltage profile and high anode utilization. PMID:25594400

  8. Rapid charge and discharge property of high capacity lithium ion battery applying three-dimensionally patterned electrode

    NASA Astrophysics Data System (ADS)

    Izumi, Akira; Sanada, Masakazu; Furuichi, Koji; Teraki, Kuniko; Matsuda, Takeshi; Hiramatsu, Kenta; Munakata, Hirokazu; Kanamura, Kiyoshi

    2014-06-01

    The cells applied with a three-dimensionally (3D) patterned Li4Ti5O12 (LTO) electrode showed good performance as a rechargeable lithium-ion battery. The 3D-patterned electrode was fabricated with a printing apparatus and has many lined patterns with a high aspect ratio standing in line on a current collector. The cell using 3D-patterned electrode showed much better rate capability than that using a conventional flat electrode. In this research, cyclic voltammetry was carried out to investigate the mechanism realizing the high rates of charging and discharging in 3D-patterned electrode. Various types of line patterns were fabricated for 3D electrode by using LTO electrode slurry, and the influences of basic specifications of electrode structure (the space between two neighboring electrode lines, the height and width of electrode) on the charge and discharge characteristics were evaluated to optimize the electrode pattern. In addition, the electrode performance was discussed from the viewpoints of ohmic resistance and charge-transfer resistance of the cells with 3D-patterned and conventional flat electrodes.

  9. Preparation of nickel nanowire arrays electrode for urea electro-oxidation in alkaline medium

    NASA Astrophysics Data System (ADS)

    Guo, Fen; Ye, Ke; Cheng, Kui; Wang, Guiling; Cao, Dianxue

    2015-03-01

    Fully metallic nickel nanowire arrays (NWAs) electrode is prepared by electrodepositing nickel within the pores and over-plating on the surface of polycarbonate template (PCT) with subsequent dissolution of the template in dichloromethane. The as-prepared electrode is characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Urea electro-oxidation reaction in KOH solution on the nickel NWAs electrode is investigated by cyclic voltammetry (CV), chronoamperometry (CA) and electrochemical impedance spectroscopy (EIS) tests. The results show that the nickel NWAs electrode achieves an onset oxidation potential of 0.25 V (vs. Ag/AgCl) and a peak current density of 160 mA cm-2 in 5 mol L-1 KOH and 0.33 mol L-1 urea accompanied with considerable stability.

  10. Indigo carmine: An organic crystal as a positive-electrode material for rechargeable sodium batteries

    NASA Astrophysics Data System (ADS)

    Yao, Masaru; Kuratani, Kentaro; Kojima, Toshikatsu; Takeichi, Nobuhiko; Senoh, Hiroshi; Kiyobayashi, Tetsu

    2014-01-01

    Using sodium, instead of lithium, in rechargeable batteries is a way to circumvent the lithium's resource problem. The challenge is to find an electrode material that can reversibly undergo redox reactions in a sodium-electrolyte at the desired electrochemical potential. We proved that indigo carmine (IC, 5,5'-indigodisulfonic acid sodium salt) can work as a positive-electrode material in not only a lithium-, but also a sodium-electrolyte. The discharge capacity of the IC-electrode was ~100 mAh g-1 with a good cycle stability in either the Na or Li electrolyte, in which the average voltage was 1.8 V vs. Na+/Na and 2.2 V vs. Li+/Li, respectively. Two Na ions per IC are stored in the electrode during the discharge, testifying to the two-electron redox reaction. An X-ray diffraction analysis revealed a layer structure for the IC powder and the DFT calculation suggested the formation of a band-like structure in the crystal.

  11. Three dimensional studies of particle failure in silicon based composite electrodes for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Gonzalez, Joseph; Sun, Ke; Huang, Meng; Lambros, John; Dillon, Shen; Chasiotis, Ioannis

    2014-12-01

    Silicon based composite electrodes for lithium ion batteries are of significant interest because of their potential to be high capacity alternatives to the commonly used graphitic carbon anodes. A drawback to their use, however, is the Si particle debonding and fracture that occurs as a result of the volumetric expansion by the lithium host particles upon lithiation of the anode electrode. We use X-ray micro computed tomography to visualize the evolution of the internal microstructure of a silicon-based electrode before and after four lithiation steps during the first half cycle of the cell. We develop a novel threshold edge detect method to perform 3D volumetric measurements of silicon particle expansion. According to our results, 100% lithiation of the composite anode resulted in up to 290% volume expansion of individual Si particles. Furthermore, the global and localized image intensity histogram profiles from 3D data were used to analyze the silicon particle X-ray attenuation effects as a function of lithiation: a decreasing attenuation with lithiation and the propagation of the reaction front through a core-shell process between the original state and 25% lithiation of the silicon-based electrode have been observed.

  12. Indigo carmine: an organic crystal as a positive-electrode material for rechargeable sodium batteries.

    PubMed

    Yao, Masaru; Kuratani, Kentaro; Kojima, Toshikatsu; Takeichi, Nobuhiko; Senoh, Hiroshi; Kiyobayashi, Tetsu

    2014-01-01

    Using sodium, instead of lithium, in rechargeable batteries is a way to circumvent the lithium's resource problem. The challenge is to find an electrode material that can reversibly undergo redox reactions in a sodium-electrolyte at the desired electrochemical potential. We proved that indigo carmine (IC, 5,5'-indigodisulfonic acid sodium salt) can work as a positive-electrode material in not only a lithium-, but also a sodium-electrolyte. The discharge capacity of the IC-electrode was ~100 mAh g(-1) with a good cycle stability in either the Na or Li electrolyte, in which the average voltage was 1.8 V vs. Na(+)/Na and 2.2 V vs. Li(+)/Li, respectively. Two Na ions per IC are stored in the electrode during the discharge, testifying to the two-electron redox reaction. An X-ray diffraction analysis revealed a layer structure for the IC powder and the DFT calculation suggested the formation of a band-like structure in the crystal. PMID:24413423

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

    NASA Astrophysics Data System (ADS)

    Lutey, Adrian H. A.; Fiorini, Maurizio; Fortunato, Alessandro; Ascari, Alessandro

    2014-12-01

    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 near the cut edge due to thermal conduction from the metallic conductive layers. The presented results provide insight into the effects of laser processing on LFP electrode integrity.

  14. Electrochemical and spectroscopic studies of carbon electrodes in lithium battery electrolyte systems

    NASA Astrophysics Data System (ADS)

    Chusid, O.; Ein Ely, E.; Aurbach, D.; Babai, M.; Carmeli, Y.

    1993-03-01

    In this work we studied several parameters that influence the intercalation of lithium ions into carbons (e.g. carbon type, binder and solution composition). The carbons investigated included carbon blacks (e.g. acetylene black, Ketjen black), graphite and carbon fibers. The solvents used in this study include methyl formate, propylene and ethylene carbonate, ethers (e.g. tetrahydrofuran) and their mixtures. The salts included LiClO 4, LiAsF 6 and LiBF 4. CO 2 was tested as an additive. The electrochemical behavior of the electrodes in solutions was followed by chronopotentiometry in galvanostatic charge/discharge cycling and their surface chemistry in solutions was investigated using surface sensitive Fourier-transform infrared spectroscopy (FT-IR) in transmittance, attenuated total reflectance and diffuse reflectance modes. It was found that the solvents and salts are reduced on the carbon electrodes at low potentials to form surface films. In general, their surface chemistry is quite similar to that of lithium or noble metal electrodes at low potential (in the same solutions). The electrochemical behavior of the carbon electrodes in terms of degree of intercalation and its reversibility is strongly affected by their surface chemistry. Reversible intercalation was obtained with graphite in methyl formate solutions containing CO 2. Some degree of reversible intercalation was also obtained with graphite in ethers. The presence of propylene carbonate in solution is detrimental for lithium intercalation in graphite. Reversible lithium-carbon intercalation was also obtained with acetylene black and carbonized polyacrylonitrile. The binder types have a strong impact on the electrode's performance. Preliminary guidelines for optimizing the performance of carbon electrodes as anodes in rechargeable lithium battery are discussed.

  15. Method of manufacturing a polymer-consolidated cadmium electrode for an alkaline storage cell, and an electrode obtained by the method

    SciTech Connect

    Brezillon, J.L.; Dauchier, J.M.

    1987-09-01

    A method is described of manufacturing a polymer-consolidated cadmium electrode for an alkaline storage cell, the method comprising the steps of: mixing the following ingredients in water: a gelling agent; cadmium and cadmium oxide in powder form constituting the active material; and a copolymer of carboxylated styrene-butadiene at a concenration lying in the range 0.5% to 3% by weight of active materials; coating the resulting paste one a metal current collector; drying the coated current collector; and subjecting the resulting assembly to a temperature lying in the range 120/sup 0/C to 150/sup 0/C for a period of a few minutes in order to cause the polymer to cross-link.

  16. Investigation of Lithium-Air Battery Discharge Product Formed on Carbon Nanotube and Nanofiber Electrodes

    NASA Astrophysics Data System (ADS)

    Mitchell, Robert Revell, III

    Carbon nanotubes have been actively investigated for integration in a wide variety of applications since their discovery over 20 years ago. Their myriad desirable material properties including exceptional mechanical strength, high thermal conductivities, large surface-to-volume ratios, and considerable electrical conductivities, which are attributable to a quantum mechanical ability to conduct electrons ballistically, have continued to motivate interest in this material system. While a variety of synthesis techniques exist, carbon nanotubes and nanofibers are most often conveniently synthesized using chemical vapor deposition (CVD), which involves their catalyzed growth from transition metal nanoparticles. Vertically-aligned nanotube and nanofiber carpets produced using CVD have been utilized in a variety of applications including those related to energy storage. Li-air (Li-O2) batteries have received much interest recently because of their very high theoretical energy densities (3200 Wh/kgLi2O2 ). which make them ideal candidates for energy storage devices for future fully-electric vehicles. During operation of a Li-air battery O2 is reduced on the surface a porous air cathode, reacting with Li-ions to form lithium peroxide (Li-O2). Unlike the intercalation reactions of Li-ion batteries, discharge in a Li-air cell is analogous to an electrodeposition process involving the nucleation and growth of the depositing species on a foreign substrate. Carbon nanofiber electrodes were synthesized on porous substrates using a chemical vapor deposition process and then assembled into Li-O2 cells. The large surface to volume ratio and low density of carbon nanofiber electrodes were found to yield a very high gravimetric energy density in Li-O 2 cells, approaching 75% of the theoretical energy density for Li 2O2. Further, the carbon nanofiber electrodes were found to be excellent platforms for conducting ex situ electron microscopy investigations of the deposition Li2O2 phase

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

    NASA Astrophysics Data System (ADS)

    Li, Yiyang; El Gabaly, Farid; Ferguson, Todd R.; Smith, Raymond B.; Bartelt, Norman C.; Sugar, Joshua D.; Fenton, Kyle R.; Cogswell, Daniel A.; Kilcoyne, A. L. David; Tyliszczak, Tolek; Bazant, Martin Z.; Chueh, William C.

    2014-12-01

    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 (LiFePO4; 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.

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

    PubMed

    Li, Yiyang; El Gabaly, Farid; Ferguson, Todd R; Smith, Raymond B; Bartelt, Norman C; Sugar, Joshua D; Fenton, Kyle R; Cogswell, Daniel A; Kilcoyne, A L David; Tyliszczak, Tolek; Bazant, Martin Z; Chueh, William C

    2014-12-01

    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 (LiFePO4; 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. PMID:25218062

  19. Ultrafast Alkaline Ni/Zn Battery Based on Ni-Foam-Supported Ni3S2 Nanosheets.

    PubMed

    Hu, Pu; Wang, Tianshi; Zhao, Jingwen; Zhang, Chuanjian; Ma, Jun; Du, Huiping; Wang, Xiaogang; Cui, Guanglei

    2015-12-01

    Self-supported Ni3S2 ultrathin nanosheets were in situ formed by direct sulfurization of commercially available nickel foam using thioacetamide as sulfur source under hydrothermal process. The morphology and structure of the as-obtained sample were analyzed by using XRD, XPS, SEM, and TEM, revealing that an ultrathin nanosheets Ni3S2 were grown on the surface of Ni form. The as-obtained Ni3S2/Ni composite with uniform architecture was used as cathode material for alkaline Ni/Zn battery, which delivered high capacity of 125 mAh g(-1) after 100 cycles with no obvious capacity fading, extraordinary rate capability (68 mAh g(-1) at the current density of 5.0 A g(-1)), and high operating voltage (1.75 V). PMID:26599523

  20. The relationship between coefficient of restitution and state of charge of zinc alkaline primary LR6 batteries

    SciTech Connect

    Bhadra, S; Hertzberg, BJ; Hsieh, AG; Croft, M; Gallaway, JW; Van Tassell, BJ; Chamoun, M; Erdonmez, C; Zhong, Z; Sholklapper, T; Steingart, DA

    2015-01-01

    The coefficient of restitution of alkaline batteries has been shown to increase as a function of depth of discharge. In this work, using non-destructive mechanical testing, the change in coefficient of restitution is compared to in situ energy-dispersive X-ray diffraction data to determine the cause of the macroscopic change in coefficient of restitution. The increase in coefficient of restitution correlates to the formation of a percolation pathway of ZnO within the anode of the cell, and the coefficient of restitution levels off at a value of 0.66 +/- 0.02 at 50% state of charge when the anode has densified into porous ZnO solid. Of note is the sensitivity of coefficient of restitution to the amount of ZnO formation that rivals the sensitivity of in situ energy-dispersive X-ray diffraction.

  1. Electrodeposited nanostructured lead dioxide as a thin film electrode for a lightweight lead-acid battery

    NASA Astrophysics Data System (ADS)

    Egan, D. R. P.; Low, C. T. J.; Walsh, F. C.

    Thin films of nanostructured lead dioxide are investigated as a positive electrode material for a lightweight lead-acid battery. The films are obtained by constant current deposition from electrolytes of lead methanesulfonate in methanesulfonic acid. The films are tested in two conditions namely (a) cyclic voltammetry and (b) constant current battery cycling in sulfuric acid. The charge and discharge current density, charge density and charge efficiency are measured as a function of cycle number. The effect of deposition conditions, such as solution temperature (295 and 333 K), type of substrate and electrolyte additive (hexadecyltrimethylammonium hydroxide), on the electrochemical performance of the PbO 2 in sulfuric acid is investigated. It is found that the as-deposited lead dioxide film is compact and nanostructured β-phase structure. Following successive cycling in sulfuric acid, the compact thin film gradually transforms into a porous microstructure consisting of positive active material (PbO 2 and PbSO 4), several tens of nanometres size. The charge density, discharge density and peak discharge current density of the PbO 2 improve with cycling of the thin film electrode.

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

    PubMed

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

    2016-09-01

    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. PMID:27518198

  3. Recent achievements on inorganic electrode materials for lithium-ion batteries.

    PubMed

    Croguennec, Laurence; Palacin, M Rosa

    2015-03-11

    The lithium-ion battery technology is rooted in the studies of intercalation of guest ions into inorganic host materials developed ca. 40 years ago. It further turned into a commercial product, which will soon blow its 25th candle. Intense research efforts during this time have resulted in the development of a large spectrum of electrode materials together with deep understanding of the underlying structure-property relationships that govern their performance. This has enabled an ever increasing electrochemical yield together with the diversification of the technology into several subfamilies, tailoring materials to application requirements. The present paper aims at providing a global and critical perspective on inorganic electrode materials for lithium-ion batteries categorized by their reaction mechanism and structural dimensionality. Specific emphasis is put on recent research in the field, which beyond the chemistry and microstructure of the materials themselves also involves considering interfacial chemistry concepts alongside progress in characterization techniques. Finally a short personal perspective is provided on some plausible development of the field. PMID:25679823

  4. Ultrathin Graphite Foam: A Three-Dimensional Conductive Network for Battery Electrodes

    SciTech Connect

    Ji, HX; Zhang, LL; Pettes, MT; Li, HF; Chen, SS; Shi, L; Piner, R; Ruoff, RS

    2012-05-01

    We report the use of free-standing, lightweight, and highly conductive ultrathin graphite foam (UGF), loaded with lithium iron phosphate (LFP), as a cathode in a lithium ion battery. At a high charge/discharge current density of 1280 mA g(-1), the specific capacity of the LFP loaded on UGF was 70 mAh g(-1), while LFP loaded on Al foil failed. Accounting for the total mass of the electrode, the maximum specific capacity of the UGF/LFP cathode was 23% higher than that of the Al/LFP cathode and 170% higher than that of the Ni-foam/LFP cathode. Using UGF, both a higher rate capability and specific capacity can be achieved simultaneously, owing to its conductive (similar to 1.3 x 10(5) S m(-1) at room temperature) and three-dimensional lightweight (similar to 9.5 mg cm(-3)) graphitic structure. Meanwhile, UGF presents excellent electrochemical stability comparing to that of Al and Ni foils, which are generally used as conductive substrates in lithium ion batteries. Moreover, preparation of the UGF electrode was facile, cost-effective, and compatible with various electrochemically active materials.

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

    PubMed

    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. PMID:27377263

  6. Rechargeable lithium sulfide electrode for a polymer tin/sulfur lithium-ion battery

    NASA Astrophysics Data System (ADS)

    Hassoun, Jusef; Sun, Yang-Kook; Scrosati, Bruno

    In this work we investigate the electrochemical behavior of a new type of carbon-lithium sulfide composite electrode. Results based on cyclic voltammetry, charge (lithium removal)-discharge (lithium acceptance) demonstrate that this electrode has a good performance in terms of reversibility, cycle life and coulombic efficiency. XRD analysis performed in situ in a lithium cell shows that lithium sulfide can be converted into sulfur during charge and re-converted back into sulfide during the following discharge process. We also show that this electrochemical process can be efficiently carried out in polymer electrolyte lithium cells and thus, that the Li 2S-C composite can be successfully used as cathode for the development of novel types of rechargeable lithium-ion sulfur batteries where the reactive and unsafe lithium metal anode is replaced by a reliable, high capacity tin-carbon composite and the unstable organic electrolyte solution is replaced by a composite gel polymer membrane that is safe, highly conductive and able to control dendrite growth across the cell. This new Sn-C/Li 2S polymer battery operates with a capacity of 600 mAh g -1 and with an average voltage of 2 V, this leading to a value of energy density amounting to 1200 Wh kg -1.

  7. Nanostructured bilayered vanadium oxide electrodes for rechargeable sodium-ion batteries.

    SciTech Connect

    Tepavcevic, S.; Xiong, H.; Stamenkovic, V.R.; Zuo, X.; Balasubramanian, M.; Prakapenka, V.B.; Johnson, C.S.; Rajh, T. )

    2012-01-01

    Tailoring nanoarchitecture of materials offers unprecedented opportunities in utilization of their functional properties. Nanostructures of vanadium oxide, synthesized by electrochemical deposition, are studied as a cathode material for rechargeable Na-ion batteries. Ex situ and in situ synchrotron characterizations revealed the presence of an electrochemically responsive bilayered structure with adjustable intralayer spacing that accommodates intercalation of Na{sup +} ions. Sodium intake induces organization of overall structure with appearance of both long- and short-range order, while deintercalation is accompanied with the loss of long-range order, whereas short-range order is preserved. Nanostructured electrodes achieve theoretical reversible capacity for Na{sub 2}V{sub 2}O{sub 5} stoichiometry of 250 mAh/g. The stability evaluation during charge-discharge cycles at room temperature revealed an efficient 3 V cathode material with superb performance: energy density of {approx}760 Wh/kg and power density of 1200 W/kg. These results demonstrate feasibility of development of the ambient temperature Na-ion rechargeable batteries by employment of electrodes with tailored nanoarchitectures.

  8. Combined NMR and PDF studies of positive electrode materials for rechargeable lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Breger, Julien

    Layered lithium nickel manganese oxides are promising, inexpensive and nontoxic alternative positive electrodes materials to the commercial LiCoO 2 electrode used in Li-ion batteries. Among these materials, Li(NiMn) 0.5O2 is particularly attractive due to its high theoretical capacity (280 mAh/g). The motivation for the research presented here was to understand the detailed long-range and short-range structure of these materials, particularly Li(NiMn)0.5O2, both as-synthesised and upon cycling. It is indeed important to know what the cation environments are, especially for the Li ions, since they strongly affect the electrochemical performance. The local environments and short-range ordering of Li(NiMn)0.5O 2, a potential Li-ion battery positive electrode material, were investigated by using a combination of X-ray and neutron diffraction and isotopic substitution (NDIS) techniques, 6Li Magic Angle Spinning (MAS) NMR spectroscopy and, for the first time, X-ray and neutron Pair Distribution Function (PDF) analysis, associated with Reverse Monte Carlo (RMC) calculations. Two Li(NiMn) 0.5O2 samples were studied in detail: one obtained from regular solid-state synthesis (SS), and another one obtained from ion-exchange routes (IE). 6Li MAS NMR experiments showed less Li/Ni site exchange (between the Li and the Ni/Mn layers) for the IE compound than for the SS compound, explaining its improved Li diffusivity and rate capability. For the SS compound, the Ni/Ni and Mn/Mn repulsion seen by PDF/RMC and the Li/Mn proximity seen by NMR were consistent with an ordering scheme intermediate between the ideal structures proposed so far (the "honey-comb" and "flower" structures). Ordering of Ni and Mn atoms in the transition metal layers was also detected in IE-Li(NiMn)0.5O2: Ni atoms tend to be surrounded by more Mn atoms in the first coordination shell, while the second coordination shell shows that zigzag ordering scheme is preferred over the chain. Ex-situ neutron diffraction

  9. Structural and electrochemical study of positive electrode materials for rechargeable lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Jiang, Meng

    The research presented in this dissertation focuses on a combined study of the electrochemistry and the structure of positive electrode materials for Li ion batteries. Li ion batteries are one of the most advanced energy storage systems and have been the subject of numerous scientific studies in recent decades. They have been widely used for various mobile devices such as cell phones, laptop computers and power tools. They are also promising candidates as power sources for automotive applications. Although intensive research has been done to improve the performance of Li ion batteries, there are still many remaining challenges to overcome so that they can be used in a wider range of applications. In particular, cheaper and safer electrodes are required with much higher reversible capacity. The series of layered nickel manganese oxides [NixLi 1/3-2x/3Mn2/3- x/3]O2 (0 < x < 1/2) are promising alternatives for Li2CoO2, the commercial positive electrode materials in Li ion batteries, because of their lower cost and higher safety and abuse tolerance, when lithium is removed from their structure. Compounds with x<1/2, in which the total Li content is higher than transition metal content, are referred as "Li-excess" materials. The "Li2MnO3-like" region is always present in this type of materials, and the overcapacity is obtained in the first charge process, which is not reversible in the following cycles. A combined X-ray diffraction, solid state nuclear magnetic resonance and X-ray absorption spectroscopy study is performed to investigate the effect of synthetic methods on the structure, to probe the structural change of the materials during cycling and to understand the electrochemical reaction mechanism. The conversion compounds are also investigated because of their high capacities. Since the various compounds have different voltage windows, they can have potential applications as both cathodes and anodes. Solid state nuclear magnetic resonance is used to study the

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

    PubMed

    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. PMID:27362635

  11. Corrosion behavior of surface treated steel in liquid sodium negative electrode of liquid metal battery

    NASA Astrophysics Data System (ADS)

    Lee, Jeonghyeon; Shin, Sang Hun; Lee, Jung Ki; Choi, Sungyeol; Kim, Ji Hyun

    2016-03-01

    While liquid metal batteries are attractive options for grid-scale energy storage applications as they have flexible siting capacities and small footprints, the compatibility between structural materials such as current collectors and negative electrode such as sodium is one of major issues for liquid metal batteries. Non-metallic elements such as carbon, oxygen, and nitrogen in the liquid sodium influence the material behaviors of the cell construction materials in the battery system. In this study, the compatibility of structural materials with sodium is investigated in high temperature liquid sodium, and electrochemical impedance spectroscopy (EIS) is used to monitor in-situ the corrosion behavior at the surface of materials in sodium. Chemical vapor deposition (CVD) coatings of SiC and Si3N4 are applied as protective barriers against dissolution and corrosion on the steel surface. The results show that CVD coating of Si compounds can delay corrosion of steel in high temperature liquid sodium comparing to the result of as-received specimens, while SiC coating is more durable than Si3N4 coating in high temperature liquid sodium.

  12. Limitation of discharge capacity and mechanisms of air-electrode deactivation in silicon-air batteries.

    PubMed

    Jakes, Peter; Cohn, Gil; Ein-Eli, Yair; Scheiba, Frieder; Ehrenberg, Helmut; Eichel, Rüdiger-A

    2012-11-01

    The electrocatalytical process at the air cathode in novel silicon-air batteries using the room-temperature ionic liquid hydrophilic 1-ethyl-3-methylimidazolium oligofluorohydrogenate [EMI⋅2.3 HF⋅F] as electrolyte and highly doped silicon wafers as anodes is investigated by electrochemical means, X-ray photoelectron spectroscopy (XPS), and electron paramagnetic resonance (EPR) spectroscopy. The results obtained by XPS and EPR provide a model to describe the limited discharge capacity by means of a mechanism of air-electrode deactivation. In that respect, upon discharge the silicon-air battery's cathode is not only blocked by silicon oxide reduction products, but also experiences a major modification in the MnO₂ catalyst nature. The proposed modification of the MnO₂ catalyst by means of a MnF₂ surface layer greatly impacts the Si-air performance and describes a mechanism relevant for other metal-air batteries, such as the lithium-air. Moreover, the ability for this deactivation layer to form is greatly impacted by water in the electrolyte. PMID:23033259

  13. Role of electrical resistance of electrodes in modeling of discharging and charging of flooded lead-acid batteries

    NASA Astrophysics Data System (ADS)

    Gandhi, K. S.

    2015-03-01

    Electrical resistance of both the electrodes of a lead-acid battery increases during discharge due to formation of lead sulfate, an insulator. Work of Metzendorf [1] shows that resistance increases sharply at about 65% conversion of active materials, and battery stops discharging once this critical conversion is reached. However, these aspects are not incorporated into existing mathematical models. Present work uses the results of Metzendorf [1], and develops a model that includes the effect of variable resistance. Further, it uses a reasonable expression to account for the decrease in active area during discharge instead of the empirical equations of previous work. The model's predictions are compared with observations of Cugnet et al. [2]. The model is as successful as the non-mechanistic models existing in literature. Inclusion of variation in resistance of electrodes in the model is important if one of the electrodes is a limiting reactant. If active materials are stoichiometrically balanced, resistance of electrodes can be very large at the end of discharge but has only a minor effect on charging of batteries. The model points to the significance of electrical conductivity of electrodes in the charging of deep discharged batteries.

  14. Quantifying Bulk Electrode Strain and Material Displacement within Lithium Batteries via High‐Speed Operando Tomography and Digital Volume Correlation

    PubMed Central

    Finegan, Donal P.; Tudisco, Erika; Scheel, Mario; Robinson, James B.; Taiwo, Oluwadamilola O.; Eastwood, David S.; Lee, Peter D.; Di Michiel, Marco; Bay, Brian; Hall, Stephen A.; Hinds, Gareth; Brett, Dan J. L.

    2015-01-01

    Tracking the dynamic morphology of active materials during operation of lithium batteries is essential for identifying causes of performance loss. Digital volume correlation (DVC) is applied to high‐speed operando synchrotron X‐ray computed tomography of a commercial Li/MnO2 primary battery during discharge. Real‐time electrode material displacement is captured in 3D allowing degradation mechanisms such as delamination of the electrode from the current collector and electrode crack formation to be identified. Continuum DVC of consecutive images during discharge is used to quantify local displacements and strains in 3D throughout discharge, facilitating tracking of the progression of swelling due to lithiation within the electrode material in a commercial, spiral‐wound battery during normal operation. Displacement of the rigid current collector and cell materials contribute to severe electrode detachment and crack formation during discharge, which is monitored by a separate DVC approach. Use of time‐lapse X‐ray computed tomography coupled with DVC is thus demonstrated as an effective diagnostic technique to identify causes of performance loss within commercial lithium batteries; this novel approach is expected to guide the development of more effective commercial cell designs. PMID:27610334

  15. Synchrotron x-ray diffraction studies of the structural properties of electrode materials in operating battery cells

    SciTech Connect

    Thurston, T.R.; Jisrawi, N.M.; Mukerjee, S.; Yang, X.Q.; McBreen, J.; Daroux, M.L.; Xing, X.K.

    1996-07-01

    Hard x rays from a synchrotron source were utilized in diffraction experiments which probed the bulk of electrode materials while they were operating {ital in} {ital situ} in battery cells. Two technologically relevant electrode materials were examined; an {ital AB}{sub 2}-type anode in a nickel{endash}metal{endash}hydride cell and a LiMn{sub 2}O{sub 4} cathode in a Li-ion {open_quote}{open_quote}rocking chair{close_quote}{close_quote} cell. Structural features such as lattice expansions and contractions, phase transitions, and the formation of multiple phases were easily observed as either hydrogen or lithium was electrochemically intercalated in and out of the electrode materials. The relevance of this technique for future studies of battery electrode materials is discussed. {copyright} {ital 1996 American Institute of Physics.}

  16. Novel nitrogen-based organosulfur electrodes for advanced intermediate temperature batteries

    NASA Technical Reports Server (NTRS)

    Visco, S. J.; Dejonghe, L. C.

    1989-01-01

    Advanced secondary batteries operating at intermediate temperatures (100 to 200 C) have attracted considerable interest due to their inherent advantages (reduced corrosion and safety risks) over higher temperature systems. Current work in this laboratory has involved research on a class of intermediate temperature Na/beta double prime- alumina/RSSR batteries conceptually similar to Na/S cells, but operating within a temperature range of 100 to 150 C, and having an organosulfur rather than inorganic sulfur positive electrode. The organosulfur electrodes are based on the reversible, two electron eduction of organodisulfides to the corresponding thiolate anions, RSSR + 2 electrons yield 2RS(-), where R is an organic moiety. Among the advantages of such a generic redox couple for battery research is the ability to tailor the physical, chemical, and electrochemical properties of the RSSR molecule through choice of the organic moiety. The viscosity, liquidus range, dielectric constant, equivalent weight, and redox potential can in fact be verified in a largely predictable manner. The current work concerns the use of multiple nitrogen organosulfur molecules, chosen for application in Na/RSSR cells for their expected oxidizing character. In fact, a Na/RSSR cell containing one of these materials, the sodium salt of 5-mercapto 1-methyltetrazole, yielded the highest open circuit voltage obtained yet in the laboratory; 3.0 volts in the charged state and 2.6 volts at 100 percent discharge. Accordingly, the cycling behavior of a series of multiple nitrogen organodisulfides as well as polymeric organodisulfides are presented in this manuscript.

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

    NASA Astrophysics Data System (ADS)

    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

  18. Black Conductive Titanium Oxide High-Capacity Materials for Battery Electrodes

    SciTech Connect

    Han, W.

    2011-05-18

    Stoichiometric titanium dioxide (TiO{sub 2}) is one of the most widely studied transitionmetal oxides because of its many potential applications in photoelectrochemical systems, such as dye-sensitized TiO{sub 2} electrodes for photovoltaic solar cells, and water-splitting catalysts for hydrogen generation, and in environmental purification for creating or degrading specific compounds. However, TiO{sub 2} has a wide bandgap and high electrical resistivity, which limits its use as an electrode. A set of non-stoichiometric titanium oxides called the Magneli phases, having a general formula of Ti{sub n}O{sub 2n-1} with n between 4 and 10, exhibits lower bandgaps and resistivities, with the highest electrical conductivities reported for Ti{sub 4}O{sub 7}. These phases have been formulated under different conditions, but in all reported cases the resulting oxides have minimum grain sizes on the order of micrometers, regardless of the size of the starting titanium compounds. In this method, nanoparticles of TiO{sub 2} or hydrogen titanates are first coated with carbon using either wet or dry chemistry methods. During this process the size and shape of the nanoparticles are 'locked in.' Subsequently the carbon-coated nanoparticles are heated. This results in the transformation of the original TiO{sub 2} or hydrogen titanates to Magneli phases without coarsening, so that the original size and shape of the nanoparticles are maintained to a precise degree. People who work on batteries, fuel cells, ultracapacitors, electrosynthesis cells, electro-chemical devices, and soil remediation have applications that could benefit from using nanoscale Magneli phases of titanium oxide. Application of these electrode materials may not be limited to substitution for TiO{sub 2} electrodes. Combining the robustness and photosensitivity of TiO{sub 2} with higher electrical conductivity may result in a general electrode material.

  19. PEDOT:PSS as multi-functional composite material for enhanced Li-air-battery air electrodes

    NASA Astrophysics Data System (ADS)

    Yoon, Dae Ho; Yoon, Seon Hye; Ryu, Kwang-Sun; Park, Yong Joon

    2016-01-01

    We propose PEDOT:PSS as a multi-functional composite material for an enhanced Li-air-battery air electrode. The PEDOT:PSS layer was coated on the surface of carbon (graphene) using simple method. A electrode containing PEDOT:PSS-coated graphene (PEDOT electrode) could be prepared without binder (such as PVDF) because of high adhesion of PEDOT:PSS. PEDOT electrode presented considerable discharge and charge capacity at all current densities. These results shows that PEDOT:PSS acts as a redox reaction matrix and conducting binder in the air electrode. Moreover, after cycling, the accumulation of reaction products due to side reaction in the electrode was significantly reduced through the use of PEDOT:PSS. This implies that PEDOT:PSS coating layer can suppress the undesirable side reactions between the carbon and electrolyte (and/or Li2O2), which causes enhanced Li-air cell cyclic performance.

  20. PEDOT:PSS as multi-functional composite material for enhanced Li-air-battery air electrodes

    PubMed Central

    Yoon, Dae Ho; Yoon, Seon Hye; Ryu, Kwang-Sun; Park, Yong Joon

    2016-01-01

    We propose PEDOT:PSS as a multi-functional composite material for an enhanced Li-air-battery air electrode. The PEDOT:PSS layer was coated on the surface of carbon (graphene) using simple method. A electrode containing PEDOT:PSS-coated graphene (PEDOT electrode) could be prepared without binder (such as PVDF) because of high adhesion of PEDOT:PSS. PEDOT electrode presented considerable discharge and charge capacity at all current densities. These results shows that PEDOT:PSS acts as a redox reaction matrix and conducting binder in the air electrode. Moreover, after cycling, the accumulation of reaction products due to side reaction in the electrode was significantly reduced through the use of PEDOT:PSS. This implies that PEDOT:PSS coating layer can suppress the undesirable side reactions between the carbon and electrolyte (and/or Li2O2), which causes enhanced Li-air cell cyclic performance. PMID:26813852

  1. Development of an electrode for lead-acid batteries possessing a high electrochemical utilization factor and invariable cycling characteristics

    NASA Astrophysics Data System (ADS)

    Yolshina, L. A.; Kudyakov, V. Ya.; Zyryanov, V. G.

    Investigations have been carried out on the deposition of compact lead layers on the surfaces of various metallic substrates. It is shown that the lead coatings so obtained are non-uniform in thickness and feature high porosities. The lead-film electrode thus produced on the surface of a fine copper grid can be used as a positive electrode in the lead-acid battery.

  2. New insights into the electrode mechanism of lithium sulfur batteries via air-free post-test analysis.

    PubMed

    Chen, Lin; Dietz Rago, Nancy L; Bloom, Ira D; Shaw, Leon L

    2016-08-01

    Effects of the volume expansion and shrinkage of Li2S cathodes on electrochemical cycle life are investigated via post-test analysis without exposure to air. The engineered electrodes that confine volume changes within micro-reactors have significantly longer life than the electrodes without the micro-reactor structure, providing the first unambiguous evidence of the importance of confining volume changes for improved battery performance. PMID:27430393

  3. General approach for high-power li-ion batteries: multiscale lithographic patterning of electrodes.

    PubMed

    Choi, Sinho; Kim, Tae-Hee; Lee, Jung-In; Kim, Jieun; Song, Hyun-Kon; Park, Soojin

    2014-12-01

    We demonstrate multiscale patterned electrodes that provide surface-area enhancement and strong adhesion between electrode materials and current collector. The combination of multiscale structured current collector and active materials (anodes and cathodes) enables us to make high-performance Li-ion batteries (LIBs). When LiFePO4 (LFP) cathode and Li4 Ti5 O12 (LTO) anode materials are combined with patterned current collectors, their electrochemical performances are significantly improved, including a high rate capability (LiFePO4 : 100 mAh g(-1) , Li4 Ti5 O12 : 60 mAh g(-1) at 100C rate) and highly stable cycling (LiFePO4 : capacity retention of 99.8% after 50 cycles at 10C rate). Moreover, we successfully fabricate full cell system consisting of patterned LFP cathode and patterned LTO anode, exhibiting high-power battery performances [capacity of approximately 70 mAh g(-1) during 1000 cycles at 10C rate (corresponding to charging/discharging time of 6 min)]. We extend this idea to Si anode that exhibits a large volume change during lithiation/delithiation process. The patterned Si electrodes show significantly enhanced electrochemical performances, including a high specific capacity (825 mAh g(-1) ) at high rate of 5C and a stable cycling retention (88% after 100 cycle at a 0.1C rate). This simple strategy can be extended to other cathode and anode materials for practical LIB applications. PMID:25333718

  4. Synthesis and Defect Structure Analysis of Complex Oxides for Li-Ion Battery Electrodes

    NASA Astrophysics Data System (ADS)

    Hao, Xiaoguang

    Lithium-ion batteries have attracted increased attention for energy storage development due to the vast demand from portable electronics, (hybrid) electric vehicles and future power grids. The research in this dissertation is focused on the development of oxide electrodes for lithium-ion batteries with high power density and improved stability. One of the promising cathodes for lithium-ion batteries is lithium manganospinel (LiMn2O4). However, this compound suffers from manganese dissolution and a Jahn-Teller distortion due to Mn3+, especially in oxygen deficient LiMn2O4-delta. Hydrothermal based synthesis methods were developed to eliminate oxygen vacancies to enable high power in cathodes composed of nano-sized spinel particles. The relationship between oxygen defects and the capacity fading mechanism was demonstrated, and collapse of the mechanical structure was identified in defect-rich LiMn 2O4-delta. Next, the nickel substituted manganospinel, LiNi0.5Mn 1.5O4 shows unexpected high voltage side reactions. To overcome this drawback, a thin and chemically inert titanate was used as an artificial SEI (solid electrolyte interface) coating to prohibit transition-metal dissolution and parasitic side reactions, which led to a 200% improvement of the capacity retention at 55°C and negligible polarization losses. Finally, the spinel-structured lithium titanate (Li 4Ti5O12) is introduced as an anode material for lithium-ion batteries due to its higher operating potential and excellent structural stability compared to current graphite anodes. However, the poor electronic conductivity and low lithium diffusion coefficient hinder its wide application. Given these advantages, a facile, low-cost solution method is explored to synthesize nano-sized titanates. Rapid charge/ discharge was achieved up to rates of 100 C (36 second charge/ discharge) due to a shorter lithium mean-free path and better contact between the active material and conductive agents.

  5. Bi-functional air electrodes for metal-air batteries. Final report, September 15, 1993--December 14, 1994

    SciTech Connect

    Swette, L.L.; Manoukian, M.; LaConti, A.B.

    1995-12-01

    The program was directed to the need for development of bifunctional air electrodes for Zn-Air batteries for the consumer market. The Zn-Air system, widely used as a primary cell for hearing-aid batteries and as a remote-site power source in industrial applications, has the advantage of high energy density, since it consumes oxygen from the ambient air utilizing a thin, efficient fuel-cell-type gas-diffusion electrode, and is comparatively low in cost. The disadvantages of the current technology are a relatively low rate capability, and the lack of simple reversibility. {open_quotes}Secondary{close_quotes} Zn-Air cells require a third electrode for oxygen evolution or mechanical replacement of the Zinc anodes; thus the development of a bifunctional air electrode (i.e., an electrode that can alternately consume and evolve oxygen) would be a significant advance in Zn-Air cell technology. Evaluations of two carbon-free non-noble metal perovskite-type catalyst systems, La{sub 1-x}CA{sub x}CoO{sub 3} as bifunctional catalysts for potential application in Zn-air batteries were carried out. The technical objectives were to develop higher-surface-area materials and to fabricate reversible electrodes by modifying the hydrophobic/hydrophilic balance of the catalyst-binder structures.

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

    PubMed Central

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

    2015-01-01

    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. PMID:26608228

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

    PubMed

    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. PMID:26808095

  8. Grid indentation analysis of mechanical properties of composite electrodes in Li-ion batteries

    DOE PAGESBeta

    Vasconcelos, Luize Scalco de; Xu, Rong; Li, Jianlin; Zhao, Kejie

    2016-03-09

    We report that electrodes in commercial rechargeable batteries are microscopically heterogeneous materials. The constituent components, including active materials, polymeric binders, and porous conductive matrix, often have large variation in their mechanical properties, making the mechanical characterization of composite electrodes a challenging task. In a model system of LiNi0.5Mn0.3Co0.2O2 cathode, we employ the instrumented grid indentation to determine the elastic modulus and hardness of the constituent phases. The approach relies on a large array of nanoindentation experiments and statistical analysis of the resulting data provided that the maximum indentation depth is carefully chosen. The statistically extracted properties of the active particlesmore » and the surrounding medium are in good agreement with the tests of targeted indentation at selected sites. Lastly, the combinatory technique of grid indentation and statistical deconvolution represents a fast and reliable route to quantify the mechanical properties of composite electrodes that feed the parametric input for the mechanics models.« less

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

    NASA Astrophysics Data System (ADS)

    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.

  10. The effect of grain size on aluminum anodes for Al-air batteries in alkaline electrolytes

    NASA Astrophysics Data System (ADS)

    Fan, Liang; Lu, Huimin

    2015-06-01

    Aluminum is an ideal material for metallic fuel cells. In this research, different grain sizes of aluminum anodes are prepared by equal channel angular pressing (ECAP) at room temperature. Microstructure of the anodes is examined by electron backscatter diffraction (EBSD) in scanning electron microscope (SEM). Hydrogen corrosion rates of the Al anodes in 4 mol L-1 NaOH are determined by hydrogen collection method. The electrochemical properties of the aluminum anodes are investigated in the same electrolyte using electrochemical impedance spectroscopy (EIS) and polarization curves. Battery performance is also tested by constant current discharge at different current densities. Results confirm that the electrochemical properties of the aluminum anodes are related to grain size. Finer grain size anode restrains hydrogen evolution, improves electrochemical activity and increases anodic utilization rate. The proposed method is shown to effectively improve the performance of Al-air batteries.

  11. Use of a copper electrode in alkaline medium as an amperometric sensor for sulphite in a flow-through configuration.

    PubMed

    Corbo, Dennys; Bertotti, Mauro

    2002-10-01

    A flow injection analysis (FIA) method has been developed for the determination of sulphite in beverages. The method is based on the amperometric detection (0.60 V vs Ag/AgCl (sat. NaCl)) of the analyte at a copper surface in an alkaline medium (1 M NaOH solution) with a manifold that incorporates flow extraction of sulphite as SO2 through a PTFE membrane. Under optimal experimental conditions the peak current response increases linearly with sulphite concentration over the range from 1.0 to 5.0 mM. The repeatability of the electrode response in the FIA configuration was evaluated as 4% ( n =20), the limit of detection of the method was 0.04 mM (S/N =3) and the analytical frequency was 50 h(-1). Since ethanol is also electroactive and permeates through the PTFE membrane, a strategy involving in a first step measurements of only ethanol by manipulating the pH of the donor stream was employed for wine samples. Then, both ethanol and sulphite were measured at the copper electrode at 0.40 V vs Ag/AgCl (sat. NaCl) and the sulphite concentration was determined by difference. Results for 3 different beverage samples (alcoholic and non-alcoholic) showed excellent agreement with the ones obtained by using a recommended procedure for sulphite analysis. PMID:12373388

  12. Binder-free and carbon-free nanoparticle batteries: a method for nanoparticle electrodes without polymeric binders or carbon black.

    PubMed

    Ha, Don-Hyung; Islam, Mohammad A; Robinson, Richard D

    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(3)O(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. PMID:22963404

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

    PubMed

    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. PMID:26844298

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

    PubMed Central

    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. PMID:26844298

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

    NASA Astrophysics Data System (ADS)

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  17. Factors determining the packing-limitation of active materials in the composite electrode of lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Kitada, Koji; Murayama, Haruno; Fukuda, Katsutoshi; Arai, Hajime; Uchimoto, Yoshiharu; Ogumi, Zempachi; Matsubara, Eiichiro

    2016-01-01

    The factors limiting the capacity of highly dense electrodes are elucidated by using composite electrodes for lithium-ion batteries, which consist of active materials LiNi1/3Co1/3Mn1/3O2 (NCM), conductive additives and binders. Electrochemical tests of such 100-μm-thick electrodes in 1 M LiPF6 electrolyte indicate that a highly dense electrode (with 18% porosity) shows a capacity density significantly lower than the other sparse electrodes on 1C charging/discharging. Detailed analysis using position sensitive in situ X-ray diffraction indicates that, unlike the other sparse electrodes, NCM on the current-collector side barely functions for this dense electrode, due to the poor accessibility of Li+ to the inner part of the electrode. Interestingly, 2 M and 0.3 M electrolytes promote the discharge and charge reactions, respectively, over the entire area of the electrode, although they exhibit lower conductivity than the 1 M electrolyte, which indicates the importance of the initial amount of Li+ in the electrolyte impregnated in the electrode pores. Thus, for a high-energy-density cell, the initial amount of Li+ and the Li+ transport significantly affect the rate capability, which governs the practical capacity of the cell under constant-current operation.

  18. Energy Harvesting by Nickel Prussian Blue Analogue Electrode in Neutralization and Mixing Entropy Batteries.

    PubMed

    Gomes, Wellington J A S; de Oliveira, Cainã; Huguenin, Fritz

    2015-08-11

    Some industries usually reduce the concentration of protons in acidic wastewater by conducting neutralization reactions and/or adding seawater to industrial effluents. This work proposes a novel electrochemical system that can harvest energy originating from entropic changes due to alteration in the concentration of sodium ions along wastewater treatment. Preparation of a self-assembled material from nickel Prussian blue analogue (NPBA) was the first step to obtain such electrochemical system. Investigation into the electrochemical properties of this material helped to evaluate its potential use in neutralization and mixing entropy batteries. Assessment of parameters such as the potentiodynamic profile of the current density as a function of the concentration of protons and sodium ions, charge capacity, and cyclability as well as the reversibility of the sodium ion electroinsertion process aided estimation of the energy storage efficiency of the system. Frequency-domain measurements and models and the proposed charge compensation mechanism provided the rate constants at different dc potentials. After each charge/discharge cycle, the NPBA electrode harvested 12.4 kJ per mol of intercalated sodium ion in aqueous solutions of NaCl at concentrations of 20 mM and 3.0 M. The full electrochemical cell consisted of an NPBA positive electrode and a negative electrode of silver particles dispersed in a polypyrrole electrode. This cell extracted 16.8 kJ per mol of intercalated ion after each charge/discharge cycle. On the basis of these results, the developed electrochemical system should encourage wastewater treatment and help to achieve sustainable growth. PMID:26192558

  19. Strategies to improve the electrochemical performance of electrodes for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Yang, Ming-Che

    Lithium-ion batteries are widely used in consumer market because of their lightweight and rechargeable property. However, for the application as power sources of hybrid electric vehicles (HEVs), which need excellent cycling performance, high energy density, high power density, capacity, and low cost, new materials still need to be developed to meet the demands. In this dissertation work, three different strategies were developed to improve the properties of the electrode of lithium batteries. First, the voltage profile and lithium diffusion battier of LiM1/2Mn 3/2O4 (M=Ti, V, Cr, Fe, Co, Ni and Cu) were predicted by first principles theory. The computation results suggest that doping with Co or Cu can potentially lower Li diffusion barrier compared with Ni doping. Our experimental research has focused on LiNixCuyMn 2-x-yO4 (0

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

    NASA Astrophysics Data System (ADS)

    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

  1. LiCoO2 and SnO2 Thin Film Electrodes for Lithium-Ion Battery Applications

    NASA Technical Reports Server (NTRS)

    Maranchi, Jeffrey P.; Hepp, Aloysius F.; Kumta, Prashant N.

    2004-01-01

    There is an increasing need for small dimension, ultra-lightweight, portable power supplies due to the miniaturization of consumer electronic devices. Rechargeable thin film lithium-ion batteries have the potential to fulfill the growing demands for micro-energy storage devices. However, rechargeable battery technology and fabrication processes have not kept paced with the advances made in device technology. Economical fabrication methods lending excellent microstructural and compositional control in the thin film battery electrodes have yet to be fully developed. In this study, spin coating has been used to demonstrate the flexibility of the approach to produce both anode (SnO2) and cathode (LiCoO2) thin films. Results on the microstructure crystal structure and electrochemical properties of the thin film electrodes are described and discussed.

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

    PubMed

    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. PMID:27076373

  3. Investigation of the properties of polyacrylamide-polyaniline composite and its application as a battery electrode

    SciTech Connect

    Bhat, N.V.; Joshi, N.V. . Dept. of Chemical Technology)

    1993-11-20

    The composite films of polyacrylamide and polyaniline were prepared by polymerizing aniline using ammonium persulfate as an initiator in an aqueous solution containing poly-acrylamide. A film was then cast from this solution. The structural, dynamic mechanical, electrical, and thermal properties of these films have been studied. The infrared spectrum shows the presence of polyacrylamide as well as polyaniline in the composite film. The thermal analysis shows that the composite degrades slower than does the polyacrylamide alone. The dynamic mechanical analysis indicates that there is an increase in the glass transition temperature after the composite formation. The electrical conductivity has been found to increase by more than eight orders of magnitude. These composite films have also been suitably used as electrodes in secondary batteries.

  4. Nanostructured lithium-aluminum alloy electrodes for lithium-ion batteries.

    SciTech Connect

    Hudak, Nicholas S.; Huber, Dale L.

    2010-12-01

    Electrodeposited aluminum films and template-synthesized aluminum nanorods are examined as negative electrodes for lithium-ion batteries. The lithium-aluminum alloying reaction is observed electrochemically with cyclic voltammetry and galvanostatic cycling in lithium half-cells. The electrodeposition reaction is shown to have high faradaic efficiency, and electrodeposited aluminum films reach theoretical capacity for the formation of LiAl (1 Ah/g). The performance of electrodeposited aluminum films is dependent on film thickness, with thicker films exhibiting better cycling behavior. The same trend is shown for electron-beam deposited aluminum films, suggesting that aluminum film thickness is the major determinant in electrochemical performance regardless of deposition technique. Synthesis of aluminum nanorod arrays on stainless steel substrates is demonstrated using electrodeposition into anodic aluminum oxide templates followed by template dissolution. Unlike nanostructures of other lithium-alloying materials, the electrochemical performance of these aluminum nanorod arrays is worse than that of bulk aluminum.

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

    SciTech Connect

    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.

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

    NASA Astrophysics Data System (ADS)

    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.

  7. Research on spray-dried lithium titanate as electrode materials for lithium ion batteries

    NASA Astrophysics Data System (ADS)

    Wen, Zhaoyin; Gu, Zhonghua; Huang, Shahua; Yang, Jianhua; Lin, Zuxiang; Yamamoto, Osamu

    Li 4Ti 5O 12 has been considered as a promising electrode material for lithium secondary batteries. In this work a spray drying process was developed to prepare porous and spherical Li 4Ti 5O 12 powders with Li 2CO 3 and rutile type TiO 2 as precursors and PVB as forming agent of pores. The experimental results showed that porous and spherical morphology of the spray-dried powders was maintained during the sintering and the subsequent heat treatment. The oxygen atmosphere was demonstrated important to the electrochemical performance of the Li 4Ti 5O 12 powders. However, overtime heat treatment would result in superfluous loss of lithium content and therefore led to obvious decrease of charge and discharge capacities.

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

    NASA Astrophysics Data System (ADS)

    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.

  9. Highly stable and ultrafast electrode reaction of graphite for sodium ion batteries

    NASA Astrophysics Data System (ADS)

    Zhu, Zhiqiang; Cheng, Fangyi; Hu, Zhe; Niu, Zhiqiang; Chen, Jun

    2015-10-01

    Sodium ion battery is a potential sustainable energy storage system due to its abundance and low cost. To date, some Na-storage anode materials have achieved long life span, but the rate performance still remains insufficient. Herein, we show that in some linear ether-based electrolytes, graphite can not only render unprecedented cyclability (∼6000 cycles), but also exhibit ultrahigh rate capability (up to 10 A g-1), along with a reversible capacity of ∼110 mAh g-1. By combining electrochemical measurements and structural analysis (e.g. in situ Raman and ex situ XRD measurements), we reveal that graphite undergoes a stage-evolution mechanism induced by the insertion of solvated sodium ions. Furthermore, kinetic studies have shown that this process accompanies with an intercalation pseudocapacitive behavior, which should be responsible for the obtained superior electrode properties.

  10. Magnetite Nanocrystals as Anode Electrode Materials for Rechargeable Li-Ion Batteries.

    PubMed

    Ma, Xiaoling; Zeng, Guoping; Chen, Gongxuan; Huang, Yuanqiao; Wu, Tian

    2015-09-01

    Monodispersed magnetite (Fe3O4) nanocrystals were synthesized and their electrochemical properties as anode electrode materials for rechargeable lithium ion batteries were measured. The magnetite anodes, in the form of monodispersed nanospheres with average diameters (< 10 nm), show particle size effects. Specifically, the first discharge curves show that the nanocrystals can hold much more Li+ per formula unit than their counterparts in bulk before the reduction begins. The electrolyte decomposition takes place before the reduction reaction is completed. The cycling performance of the Fe3O4 nanocrystals after being heated at 300 degrees C for different lengths of time show that heating can improve the integration of the nanocrystals and increase their capacity retention in consequence. PMID:26716309

  11. A novel high capacity positive electrode material with tunnel-type structure for aqueous sodium-ion batteries

    DOE PAGESBeta

    Wang, Yuesheng; Mu, Linqin; Liu, Jue; Yang, Zhenzhong; Yu, Xiqian; Gu, Lin; Hu, Yong -Sheng; Li, Hong; Yang, Xiao -Qing; Chen, Liquan; et al

    2015-08-06

    In this study, aqueous sodium-ion batteries have shown desired properties of high safety characteristics and low-cost for large-scale energy storage applications such as smart grid, because of the abundant sodium resources as well as the inherently safer aqueous electrolytes. Among various Na insertion electrode materials, tunnel-type Na0.44MnO2 has been widely investigated as a positive electrode for aqueous sodium-ion batteries. However, the low achievable capacity hinders its practical applications. Here we report a novel sodium rich tunnel-type positive material with a nominal composition of Na0.66[Mn0.66Ti0.34]O2. The tunnel-type structure of Na0.44MnO2 obtained for this compound was confirmed by XRD and atomic-scale STEM/EELS.more » When cycled as positive electrode in full cells using NaTi2(PO4)3/C as negative electrode in 1M Na2SO4 aqueous electrolyte, this material shows the highest capacity of 76 mAh g-1 among the Na insertion oxides with an average operating voltage of 1.2 V at a current rate of 2C. These results demonstrate that Na0.66[Mn0.66Ti0.34]O2 is a promising positive electrode material for rechargeable aqueous sodium-ion batteries.« less

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

    PubMed

    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. PMID:25677246

  13. Carbon inverse opal entrapped with electrode active nanoparticles as high-performance anode for lithium-ion batteries

    PubMed Central

    Huang, Xin; Chen, Jing; Lu, Ziyang; Yu, Hong; Yan, Qingyu; Hng, Huey Hoon

    2013-01-01

    Enhancing ion and electron transport kinetics together with improving cycle life are important issues to be considered when developing high-performance Li ion batteries. Here we demonstrate a three dimensional ordered macroporous conductive electrode concept by entrapping electrode active nanoparticles in an interpenetrating macroporous carbon inverse opal. The electrodes are featured with simultaneously enhanced ion and electron transport kinetics as well as geometrically constrained active nanoparticles. The electrode can deliver up to 94.17% of theoretical capacity over 1000 discharge/charge cycles at a current density of 2.0 A g−1, and exhibits good rate capability in the high current density range of 1.0–10.0 A g−1. We hope that our findings will help pave the way for tailored design of many other sophisticated electrode materials in electrochemistry. PMID:23897089

  14. Characterization of Electrode Materials for Lithium Ion and Sodium Ion Batteries Using Synchrotron Radiation Techniques

    PubMed Central

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

    2013-01-01

    Intercalation compounds such as transition metal oxides or phosphates are the most commonly used electrode materials in Li-ion and Na-ion batteries. During insertion or removal of alkali metal ions, the redox states of transition metals in the compounds change and structural transformations such as phase transitions and/or lattice parameter increases or decreases occur. These behaviors in turn determine important characteristics of the batteries such as the potential profiles, rate capabilities, and cycle lives. The extremely bright and tunable x-rays produced by synchrotron radiation allow rapid acquisition of high-resolution data that provide information about these processes. Transformations in the bulk materials, such as phase transitions, can be directly observed using X-ray diffraction (XRD), while X-ray absorption spectroscopy (XAS) gives information about the local electronic and geometric structures (e.g. changes in redox states and bond lengths). In situ experiments carried out on operating cells are particularly useful because they allow direct correlation between the electrochemical and structural properties of the materials. These experiments are time-consuming and can be challenging to design due to the reactivity and air-sensitivity of the alkali metal anodes used in the half-cell configurations, and/or the possibility of signal interference from other cell components and hardware. For these reasons, it is appropriate to carry out ex situ experiments (e.g. on electrodes harvested from partially charged or cycled cells) in some cases. Here, we present detailed protocols for the preparation of both ex situ and in situ samples for experiments involving synchrotron radiation and demonstrate how these experiments are done. PMID:24300777

  15. Characterization of electrode materials for lithium ion and sodium ion batteries using synchrotron radiation techniques.

    PubMed

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

    2013-01-01

    Intercalation compounds such as transition metal oxides or phosphates are the most commonly used electrode materials in Li-ion and Na-ion batteries. During insertion or removal of alkali metal ions, the redox states of transition metals in the compounds change and structural transformations such as phase transitions and/or lattice parameter increases or decreases occur. These behaviors in turn determine important characteristics of the batteries such as the potential profiles, rate capabilities, and cycle lives. The extremely bright and tunable x-rays produced by synchrotron radiation allow rapid acquisition of high-resolution data that provide information about these processes. Transformations in the bulk materials, such as phase transitions, can be directly observed using X-ray diffraction (XRD), while X-ray absorption spectroscopy (XAS) gives information about the local electronic and geometric structures (e.g. changes in redox states and bond lengths). In situ experiments carried out on operating cells are particularly useful because they allow direct correlation between the electrochemical and structural properties of the materials. These experiments are time-consuming and can be challenging to design due to the reactivity and air-sensitivity of the alkali metal anodes used in the half-cell configurations, and/or the possibility of signal interference from other cell components and hardware. For these reasons, it is appropriate to carry out ex situ experiments (e.g. on electrodes harvested from partially charged or cycled cells) in some cases. Here, we present detailed protocols for the preparation of both ex situ and in situ samples for experiments involving synchrotron radiation and demonstrate how these experiments are done. PMID:24300777

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

    PubMed

    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. PMID:26082019

  17. A new class of lithium and sodium rechargeable batteries based on selenium and selenium-sulfur as a positive electrode.

    PubMed

    Abouimrane, Ali; Dambournet, Damien; Chapman, Karena W; Chupas, Peter J; Weng, Wei; Amine, Khalil

    2012-03-14

    A new class of selenium and selenium-sulfur (Se(x)S(y))-based cathode materials for room temperature lithium and sodium batteries is reported. The structural mechanisms for Li/Na insertion in these electrodes were investigated using pair distribution function (PDF) analysis. Not only does the Se electrode show promising electrochemical performance with both Li and Na anodes, but the additional potential for mixed Se(x)S(y) systems allows for tunable electrodes, combining the high capacities of S-rich systems with the high electrical conductivity of the d-electron containing Se. Unlike the widely studied Li/S system, both Se and Se(x)S(y) can be cycled to high voltages (up to 4.6 V) without failure. Their high densities and voltage output offer greater volumetric energy densities than S-based batteries, opening possibilities for new energy storage systems that can enable electric vehicles and smart grids. PMID:22364225

  18. Electrochemical characterisation of activated carbon particles used in redox flow battery electrodes

    NASA Astrophysics Data System (ADS)

    Radford, G. J. W.; Cox, J.; Wills, R. G. A.; Walsh, F. C.

    The Faradaic and non-Faradaic characteristics of a series of activated carbon particles (used to produce composite carbon-polymer electrodes for redox flow cells) have been determined using aqueous electrolytes (sulfuric acid and sodium polysulfide) at 295 K. The particles were mounted as a circular section (ca. 0.80 cm 2) shallow packed bed of 2.5 mm thickness in the direction of electrolyte flow (mean linear flow velocity ≈ 6 mm s -1). Cyclic voltammetry in deaerated, 1 mol dm -3 H 2SO 4 at 295 K indicated a specific capacitance in the range of 50-140 F g -1. Linear sweep voltammetry and galvanostatic step studies in an alkaline sodium polysulfide electrolyte (1.8 mol dm -3 Na 2S 2.11) have demonstrated marked differences amongst various types of activated carbon. Such differences are highlighted during galvanostatic charge-discharge cycling of half-cell electrodes in the polysulfide electrolyte. The electrochemical characteristics are compared to those based on (N 2 adsorption) gas porosimetry measurements.

  19. Electrical, mechanical and morphological properties of compressed carbon felt electrodes in vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Chang, Tien-Chan; Zhang, Jun-Pu; Fuh, Yiin-Kuen

    2014-01-01

    Experiments including electrical, mechanical and morphological aspects under compression in the range of 0-40% have been carried out on four potential materials for liquid diffusion layer (LDL) of vanadium redox flow battery (VRB) (including three widely used carbon felt and one recently utilized metal foam) in order to better understand the influence of the fundamental properties on the battery performance. We experimentally demonstrate that the electrical contact resistance is predominately determined by the clamping force. It is observed that increasing the stress applied on the carbon felt, which is of high interest for the durability of the membrane electrode assembly (MEA), has moreover a positive effect on their performance due to the reduced contact resistance. However, a simultaneously reduced porosity is also recorded and possibly detrimental to the mass transport of vanadium electrolyte. Moreover, the intrusion of carbon felts under compression is also characterized. Experimental results show that with the clamping force increases, both the porosity of the carbon felts underneath the rib and channel volume decrease, and this can be mainly attributed to the deformation of the carbon felts and resultant changed of the void volume as well as intrusion.

  20. Nickel hexacyanoferrate nanoparticle electrodes for aqueous sodium and potassium ion batteries.

    PubMed

    Wessells, Colin D; Peddada, Sandeep V; Huggins, Robert A; Cui, Yi

    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. PMID:22043814

  1. Properties of a carbon negative electrode in completely inorganic thin film Li-ion batteries with a LiCoO{sub 2} positive electrode

    SciTech Connect

    Goldner, R.B.; Slaven, S.; Liu, T.Y.

    1995-10-01

    Completely inorganic thin film lithium ion battery cells have been prepared by vapor deposition processes (vacuum evaporation and sputtering). The negative and positive electrodes were films of disordered carbon and lithium cobalt oxide, respectively. The results of battery charging/discharging and other measurements (e.g., in-situ lithium chemical diffusion constant measurements for the carbon films) indicate that disordered carbon films have a relatively high reversible charge capacity, (> 160 mC/cm{sup 2}-{mu}m, and possibly higher than 360 mC/cm{sup 2}-{mu}m, or > 296 and possibly 667 mAh/g, respectively, assuming the measured film density of 1.5g/cm{sup 3}), and a lithium chemical diffusion constant at room temperature {approximately}10{sup -9} cm{sup 2}/s. These results suggest that disordered carbon films should be good substitutes for metallic lithium in thin film rechargeable batteries.

  2. Determination of the zincate diffusion coefficient and its application to alkaline battery problems

    NASA Technical Reports Server (NTRS)

    May, C. E.; Kautz, Harold E.

    1978-01-01

    The diffusion coefficient for the zincate ion at 24 C was found to be 9.9 X 10 to the minus 7th power squared cm per sec + or - 30 percent in 45 percent potassium hydroxide and 1.4 x 10 to the minus 7 squared cm per sec + or - 25 percent in 40 percent sodium hydroxide. Comparison of these values with literature values at different potassium hydroxide concentrations show that the Stokes-Einstein equation is obeyed. The diffusion coefficient is characteristic of the zincate ion (not the cation) and independent of its concentration. Calculations with the measured value of the diffusion coefficient show that the zinc concentration in an alkaline zincate half cell becomes uniform throughout in tens of hours by diffusion alone. Diffusion equations are derived which are applicable to finite size chambers. Details and discussion of the experimental method are also given.

  3. Determination of the zincate diffusion coefficient and its application to alkaline battery problems

    NASA Technical Reports Server (NTRS)

    May, C. E.; Kautz, H. E.

    1978-01-01

    The diffusion coefficient for the zincate ion at 24 C was found to be 9.9 x 10 to the -7th power sq cm/sec + or - 30% in 45% potassium hydroxide and 1.4 x 10 to the -7th power sq cm/sec + or - 25% in 40% sodium hydroxide. Comparison of these values with literature values at different potassium hydroxide concentrations show that the Stokes-Einstein equation is obeyed. The diffusion coefficient is characteristic of the zincate ion (not the cation) and independent of its concentration. Calculations with the measured value of the diffusion coefficient show that the zinc concentration in an alkaline zincate half-cell becomes uniform throughout in tens of hours by diffusion alone. Diffusion equations are derived which are applicable to finite-size chambers. Details and discussion of the experimental method are also given.

  4. Transmission electron microscopy (TEM) investigations of Mn-oxide rich cathodic material from spent disposable alkaline batteries

    SciTech Connect

    Krekeler, Mark P.S.

    2008-11-15

    Transmission electron microscopy (TEM) techniques were used to investigate the spent cathodic material of a single common brand of disposable alkaline batteries. Mn-oxide particles are anhedral and irregular in shape and compose an estimated 99-95% of the <10 {mu}m size fraction of sample material. Diameters of particles vary widely and typically are between 50 nm and 3 {mu}m; however, most particles are approximately 200-400 nm in diameter. Chemical composition varies for Mn-oxide particles with concentrations being SiO{sub 2} (0.00-1.52 wt%), TiO{sub 2} (0.49-4.58 wt%), MnO (65.85-92.06 wt%), ZnO (1.00-7.53 wt%), K{sub 2}O (4.97-20.48 wt%) and SO{sub 3} (0.43-2.21 wt%). Discrete prismatic zinc crystals occur and vary from a maximum of approximately 0.8 {mu}m long x 0.15 {mu}m wide, to 100 nm long x 20 nm wide. Titanium metal was also observed in samples and composes approximately 0.25-1.0% of the <10 {mu}m size fraction of sample material. Results of this study suggest that battery components may be recycled in some special applications. Examples are low energy-low material requirement products such as paint pigments and Zn nanoparticles. This investigation provides detailed constraints on the nature of spent cathodic materials to improve existing recycling methods and develop new technologies.

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

    PubMed

    Wessells, Colin D; Huggins, Robert A; Cui, Yi

    2011-01-01

    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 17 C rate, 83% of the original capacity of copper hexacyanoferrate is retained. Even at a very high cycling rate of 83 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. PMID:22109524

  6. Physics of electron and lithium-ion transport in electrode materials for Li-ion batteries

    NASA Astrophysics Data System (ADS)

    Musheng, Wu; Bo, Xu; Chuying, Ouyang

    2016-01-01

    The physics of ionic and electrical conduction at electrode materials of lithium-ion batteries (LIBs) are briefly summarized here, besides, we review the current research on ionic and electrical conduction in electrode material incorporating experimental and simulation studies. Commercial LIBs have been widely used in portable electronic devices and are now developed for large-scale applications in hybrid electric vehicles (HEV) and stationary distributed power stations. However, due to the physical limits of the materials, the overall performance of today’s LIBs does not meet all the requirements for future applications, and the transport problem has been one of the main barriers to further improvement. The electron and Li-ion transport behaviors are important in determining the rate capacity of LIBs. Project supported by the National High Technology Research and Development Program of China (Grant No. 2015AA034201), the National Natural Science Foundation of China (Grant Nos. 11234013 and 11264014), the Natural Science Foundation of Jiangxi Province, China (Grant Nos. 20133ACB21010 and 20142BAB212002), and the Foundation of Jiangxi Education Committee, China (Grant Nos. GJJ14254 and KJLD14024). C. Y. Ouyang is also supported by the “Gan-po talent 555” Project of Jiangxi Province, China.

  7. Three-Dimensional Au Microlattices as Positive Electrodes for Li-O2 Batteries.

    PubMed

    Xu, Chen; Gallant, Betar M; Wunderlich, Phillip U; Lohmann, Timm; Greer, Julia R

    2015-06-23

    We demonstrate the feasibility of using a 3-dimensional gold microlattice with a periodic porous structure and independently tunable surface composition as a Li-O2 battery cathode. The structure provides a platform for studying electrochemical reactions in architected Li-O2 electrodes with large (300 μm) pore sizes. The lack of carbon and chemical binders in these Au microlattices enabled the investigation of chemical and morphological processes that occur on the surfaces of the microlattice during cycling. Li-O2 cells with Au microlattice cathodes were discharged in 0.5 M lithium-bis(trifluoromethane)sulfonamide (LiTFSI) in a 1,2-dimethoxyethane (DME) electrolyte, with lithium metal foil as the anode. SEM analysis of microlattice cathodes after first discharge revealed the presence of toroidal-shaped 500-700 nm particles covering the surface of the electrode, which disappeared upon subsequent charging. Raman and FTIR spectroscopy analysis determined these particulates to be Li2O2. The morphology of discharge products evolved with cycling into micrometer-sized clusters of arranged "platelets", with a higher amount of side reaction products such as Li2CO3 and LiOH. This work shows that properly designed 3-dimensional architected materials may provide a useful foundation for investigating fundamental surface electrochemistry while simultaneously enabling mechanical robustness and enhancing the surface area over a factor of 30 compared with a thin film with the same foot print. PMID:25950649

  8. The transformation of graphite electrode materials in lithium-ion batteries after cycling

    NASA Astrophysics Data System (ADS)

    Dai, Kehua; Wang, Zhihui; Ai, Guo; Zhao, Hui; Yuan, Wen; Song, Xiangyun; Battaglia, Vincent; Sun, Chengdong; Wu, Kai; Liu, Gao

    2015-12-01

    To reveal how graphite electrodes change with cycling in lithium-ion batteries, electrochemical experiments involving charge-discharge cycling at different current density conditions are performed on commercial pouch cells and the graphite electrodes after cycling. This research shows that the polyvinylidene fluoride (PVDF) binder does not degrade, confirmed by the stable molecular weight after different cycling conditions. Particle size analysis results indicate that the diameter of graphite particles after cycling is ∼10% larger than that of the graphite before cycling, which results in a ∼30% volume expansion after cycling. For the cells cycled at the same current density, the graphite particle size increases with cycle time. For the cells with the same cycle numbers, the graphite particle size is larger in the cells cycled at lower current density. X-ray diffraction characterization shows that the d-spacings of the graphite particles in all the cells at different cycling conditions are identical. These results suggest that the graphite particle size increase associated with cycling may arise specifically when primary particles inflate the secondary particle size, leading to dramatic volume expansion of graphite secondary particles.

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

    NASA Astrophysics Data System (ADS)

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

    NASA Astrophysics Data System (ADS)

    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.

  11. 3D Graphene Functionalized by Covalent Organic Framework Thin Film as Capacitive Electrode in Alkaline Media.

    PubMed

    Zha, Zeqi; Xu, Lirong; Wang, Zhikui; Li, Xiaoguang; Pan, Qinmin; Hu, Pingan; Lei, Shengbin

    2015-08-19

    To harness the electroactivity of anthraquinone as an electrode material, a great recent effort have been invested to composite anthraquinone with carbon materials to improve the conductivity. Here we report on a noncovalent way to modify three-dimensional graphene with anthraquinone moieties through on-surface synthesis of two-dimensional covalent organic frameworks. We incorporate 2,6-diamino-anthraquinone moieties into COF through Schiff-base reaction with benzene-1,3,5-tricarbaldehyde. The synthesized COF -graphene composite exhibits large specific capacitance of 31.7 mF/cm(2). Long-term galvanostatic charge/discharge cycling experiments revealed a decrease of capacitance, which was attributed to the loss of COF materials and electrostatic repulsion accumulated during charge-discharge circles which result in the poor electrical conductivity between 2D COF layers. PMID:26203782

  12. A zero-strain layered metal oxide as the negative electrode for long-life sodium-ion batteries.

    PubMed

    Wang, Yuesheng; Yu, Xiqian; Xu, Shuyin; Bai, Jianming; Xiao, Ruijuan; Hu, Yong-Sheng; Li, Hong; Yang, Xiao-Qing; Chen, Liquan; Huang, Xuejie

    2013-01-01

    Room-temperature sodium-ion batteries have shown great promise in large-scale energy storage applications for renewable energy and smart grid because of the abundant sodium resources and low cost. Although many interesting positive electrode materials with acceptable performance have been proposed, suitable negative electrode materials have not been identified and their development is quite challenging. Here we introduce a layered material, P2-Na0.66[Li0.22Ti0.78]O2, as the negative electrode, which exhibits only ~0.77% volume change during sodium insertion/extraction. The zero-strain characteristics ensure a potentially long cycle life. The electrode material also exhibits an average storage voltage of 0.75 V, a practical usable capacity of ca. 100 mAh g(-1), and an apparent Na(+) diffusion coefficient of 1 × 10(-10) cm(-2) s(-1) as well as the best cyclability for a negative electrode material in a half-cell reported to date. This contribution demonstrates that P2-Na0.66[Li0.22Ti0.78]O2 is a promising negative electrode material for the development of rechargeable long-life sodium-ion batteries. PMID:23978932

  13. Thin electrodes based on rolled Pb-Sn-Ca grids for VRLA batteries

    NASA Astrophysics Data System (ADS)

    Caballero, A.; Cruz, M.; Hernán, L.; Morales, J.; Sánchez, L.

    Electrodes 0.5 mm thick (i.e. much thinner than conventional ones) and suitable for lead-acid batteries were prepared by using a special pasting procedure that allows plate thickness to be readily controlled. Novel rolled grids of Pb-Sn-low Ca alloys (0.35 mm thick) were used as substrates. Preliminary galvanostatic corrosion tests of the grids revealed an increased corrosion rate relative to conventional casted grids of Pb-Sn alloys (1 mm thick). Cells made with these thin electrodes were cycled under different discharge regimes and the active material at different charge/discharge cycling stages was characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and chemical analysis. At a depth of discharge (DOD) of 100%, the cell exhibited a premature capacity loss after the fifth cycle and delivered only a 20% of its nominal capacity after the 10th. By contrast, cycling performance of the electrode was significantly improved at a DOD of 60%. The capacity loss observed at a DOD of 100% can be ascribed to a rapid growth of PbSO 4 crystals reaching several microns in size. Such large crystals tend to deposit onto the grid surface and form an insulating layer that hinders electron transfer at the active material/grid interface. For this reason, the cell fails after few cycles in spite of the high PbO 2 content in the positive active material (PAM). On the other hand, at 60% DOD the submicronic particles produced after formation of the PAM retain their small size, thereby ensuring reversibility in the PbO 2⇔PbSO 4 transformation.

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

    PubMed

    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). PMID:26700975

  15. Biomimetic nanostructuring of copper thin films enhances adhesion to the negative electrode laminate in lithium-ion batteries.

    PubMed

    Zheng, Ziyan; Wang, Zhihui; Song, Xiangyun; Xun, Shidi; Battaglia, Vincent; Liu, Gao

    2014-10-01

    Thin films of copper are widely used as current collectors for the negative electrodes in lithium-ion batteries. However, a major cause of battery failure is delamination between the current collector and the graphite anode. When silicon or tin is used as active material, delamination becomes a key issue owing to the large volume changes of these materials during lithation and delithation processes. Learning from Nature, we developed a new biomimetic approach based on the adhesion properties of the feet of geckos. The biomimetic approach improves adhesion between the laminate and the copper surface by introducing an array of Cu(OH)2 nanorods, which increases the surface area of the current collector. When graphite anode laminate is casted onto regular and a modified copper surfaces, the modified current collector displays superior adhesion to graphite and the PVDF binder-based electrode. The electrochemical performance of the batteries using these electrodes is not compromised by the additional chemistry of the Cu(OH)2 on the copper surface. The technique can lead to enhanced battery lifetimes over long-term cycling. PMID:25139044

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

    PubMed

    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. PMID:27357533

  17. Thermal-stability studies of electrode materials for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Jiang, Junwei

    2005-07-01

    The thermal stability of lithium-ion batteries has recently attracted attention for two major reasons. (1) Attempts to make large-size cells used in power tools, E-bikes and EVs. Large cells have lower surface area to volume ratios and hence heat dissipation is more problematic than 18650-size cells. Safety problems, therefore, for large cells are more serious. (2) Next generation high-capacity electrodes will increase the energy density of lithium-ion cells meaning even an 18650-size cell may face safety concerns. This thesis presents studies of the thermal stability of electrode materials in electrolytes to understand their reactivity. A search for new positive electrode materials with high thermal stability was made. The thermal stability of two common electrode materials (Li0.81 C6 and Li0.5CoO2) in lithium-ion cells was studied by Accelerating Rate Calorimeter (ARC). Li0.81C 6 has much lower reactivity with lithium bis(oxalato)borate (LiBOB) electrolyte compared to LiPF6 electrolyte. It is not the case, however, for Li0.5CoO2. Oven tests of full LiCoO 2/C 18650-size cells with LiBOB or LiPF6 electrolytes, confirmed the ARC results. ARC was then used to study the reactivity of existing electrode materials. The thermal stability of a negative electrode material was found to increase with the binding energy of Li atoms hosted in the material. Li0.5VO 2 (B) has a higher lithium binding energy (2.45 eV vs. Li) than Li 0.81C6 (0.1 eV vs. Li) and Li7Ti5O 12 (1.55 eV) and it shows the highest thermal stability in EC/DEC among the three materials. The reactivity of two existing positive electrode materials, LiMn2O4 and LiFePO4, was studied. Cell systems expected to be highly tolerant to thermal abuse were suggested: LiFePO 4/C or Li4Ti5O12 in LiBOB electrolytes. The system, x Li[Ni1/2Mn1/2]O2 • y LiCoO2 • z Li[Li1/3Mn2/3]O2 (x + y + z = 1), was explored for new positive electrode materials with large capacity and high thermal stability. Li[(Ni0.5Mn0.5) xCo1-x]O2 (0

  18. Effect of Polymer Electrode Morphology on Performance of a Lithium/Polypyrrole Battery. M.S. Thesis

    NASA Technical Reports Server (NTRS)

    Nicholson, Marjorie Anne

    1991-01-01

    A variety of conducting polymer batteries were described in the recent literature. In this work, a Li/Polypyrrole secondary battery is described. The effect of controlling the morphology of the polymer on enhancement of counterion diffusion in the polymer phase is explored. A method of preparing conducting polymers was developed which yields high surface area per unit volume of electrode material. A porous membrane is used as a template in which to electrochemically polymerize pyrrole, then the membrane is dissolved, leaving the polymer in a fibrillar form. Conventionally, the polymer is electrochemically polymerized as a dense polymer film on a smooth Pt disk electrode. Previous work has shown that when the polymer is electrochemically polymerized in fribrillar form, charge transport rates are faster and charge capacities are greater than for dense, conventionally grown films containing the same amount of polymer. The purpose is to expand previous work by further investigating the possibilities of the optimization of transport rates in polypyrrole films by controlling the morphology of the films. The utility of fibrillar polypyrrole as a cathode material in a lithium/polymer secondary battery is then assessed. The performance of the fibrillar battery is compared to the performance of an analogous battery which employed a conventionally grown polypyrrole film. The study includes a comparison of cyclic voltammetry, shape of charge/discharge curves, discharge time and voltage, cycle life, coulombic efficiencies, charge capacities, energy densities, and energy efficiencies.

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

    SciTech Connect

    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.

  20. A Convenient and Versatile Method To Control the Electrode Microstructure toward High-Energy Lithium-Ion Batteries.

    PubMed

    Zhao, Hui; Yang, Qing; Yuca, Neslihan; Ling, Min; Higa, Kenneth; Battaglia, Vincent S; Parkinson, Dilworth Y; Srinivasan, Venkat; Liu, Gao

    2016-07-13

    Control over porous electrode microstructure is critical for the continued improvement of electrochemical performance of lithium ion batteries. This paper describes a convenient and economical method for controlling electrode porosity, thereby enhancing material loading and stabilizing the cycling performance. Sacrificial NaCl is added to a Si-based electrode, which demonstrates an areal capacity of ∼4 mAh/cm(2) at a C/10 rate (0.51 mA/cm(2)) and an areal capacity of 3 mAh/cm(2) at a C/3 rate (1.7 mA/cm(2)), one of the highest material loadings reported for a Si-based anode at such a high cycling rate. X-ray microtomography confirmed the improved porous architecture of the SiO electrode with NaCl. The method developed here is expected to be compatible with the state-of-the-art lithium ion battery industrial fabrication processes and therefore holds great promise as a practical technique for boosting the electrochemical performance of lithium ion batteries without changing material systems. PMID:27336856