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Sample records for air electrode material

  1. Method of making an air electrode material having controlled sinterability

    DOEpatents

    Vasilow, Theodore R.; Kuo, Lewis J. H.; Ruka, Roswell J.

    1994-01-01

    A tubular, porous ceramic electrode structure (3) is made from the sintered admixture of doped lanthanum manganite and an additive containing cerium where a solid electrolyte (4), substantially surrounds the air electrode, and a porous outer fuel electrode (7) substantially surrounds the electrolyte, to form a fuel cell (1).

  2. 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.

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

    NASA Astrophysics Data System (ADS)

    Ross, Philip N., Jr.

    1988-06-01

    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.

  4. 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

  5. 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.

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

    DOEpatents

    Ross, Jr., Philip N.

    1990-01-01

    A novel carbonaceous electrode support material is disclosed characterized by a corrosion rate of 0.03 wt. %/hour or less when measured a5 550 millivolts vs. a Hg/HgO electrode in a 30 wt. % KOH electrolyte a5 30.degree. C. The electrode support material comprises a preselected carbon black material which has been heat-treated by heating the material to a temperature of from about 2500.degree. to about 3000.degree. C. over a period of from about 1 to about 5 hours in an inert atmosphere and then maintaining the preselected carbon black material at this temperature for a period of at least about 1 hour, and preferably about 2 hours, in the inert atmosphere. A carbonaceous electrode suitable for use as an air electrode in a metal-air cell may be made from the electrode support material by shaping and forming it into a catalyst support and then impregnating it with a catalytically active material capable of catalyzing the reaction with oxygen at the air electrode of metal-air cell.

  7. Low cost stable air electrode material for high temperature solid oxide electrolyte electrochemical cells

    DOEpatents

    Kuo, Lewis J. H.; Singh, Prabhakar; Ruka, Roswell J.; Vasilow, Theodore R.; Bratton, Raymond J.

    1997-01-01

    A low cost, lanthanide-substituted, dimensionally and thermally stable, gas permeable, electrically conductive, porous ceramic air electrode composition of lanthanide-substituted doped lanthanum manganite is provided which is used as the cathode in high temperature, solid oxide electrolyte fuel cells and generators. The air electrode composition of this invention has a much lower fabrication cost as a result of using a lower cost lanthanide mixture, either a natural mixture or an unfinished lanthanide concentrate obtained from a natural mixture subjected to incomplete purification, as the raw material in place of part or all of the higher cost individual lanthanum. The mixed lanthanide primarily contains a mixture of at least La, Ce, Pr, and Nd, or at least La, Ce, Pr, Nd and Sm in its lanthanide content, but can also include minor amounts of other lanthanides and trace impurities. The use of lanthanides in place of some or all of the lanthanum also increases the dimensional stability of the air electrode. This low cost air electrode can be fabricated as a cathode for use in high temperature, solid oxide fuel cells and generators.

  8. Low cost stable air electrode material for high temperature solid oxide electrolyte electrochemical cells

    DOEpatents

    Kuo, L.J.H.; Singh, P.; Ruka, R.J.; Vasilow, T.R.; Bratton, R.J.

    1997-11-11

    A low cost, lanthanide-substituted, dimensionally and thermally stable, gas permeable, electrically conductive, porous ceramic air electrode composition of lanthanide-substituted doped lanthanum manganite is provided which is used as the cathode in high temperature, solid oxide electrolyte fuel cells and generators. The air electrode composition of this invention has a much lower fabrication cost as a result of using a lower cost lanthanide mixture, either a natural mixture or an unfinished lanthanide concentrate obtained from a natural mixture subjected to incomplete purification, as the raw material in place of part or all of the higher cost individual lanthanum. The mixed lanthanide primarily contains a mixture of at least La, Ce, Pr, and Nd, or at least La, Ce, Pr, Nd and Sm in its lanthanide content, but can also include minor amounts of other lanthanides and trace impurities. The use of lanthanides in place of some or all of the lanthanum also increases the dimensional stability of the air electrode. This low cost air electrode can be fabricated as a cathode for use in high temperature, solid oxide fuel cells and generators. 4 figs.

  9. Solid oxide fuel cells, and air electrode and electrical interconnection materials therefor

    DOEpatents

    Bates, J.L.

    1992-09-01

    In one aspect of the invention, an air electrode material for a solid oxide fuel cell comprises Y[sub 1[minus]a]Q[sub a]MnO[sub 3], where Q is selected from the group consisting of Ca and Sr or mixtures thereof and a' is from 0.1 to 0.8. Preferably, a' is from 0.4 to 0.7. In another aspect of the invention, an electrical interconnection material for a solid oxide fuel cell comprises Y[sub 1[minus]b]Ca[sub b]Cr[sub 1[minus]c]Al[sub c]O[sub 3], where b' is from 0.1 to 0.6 and c' is from 0 to 9.3. Preferably, b' is from 0.3 to 0.5 and c' is from 0.05 to 0.1. A composite solid oxide electrochemical fuel cell incorporating these materials comprises: a solid oxide air electrode and an adjacent solid oxide electrical interconnection which commonly include the cation Y, the air electrode comprising Y[sub 1[minus]a]Q[sub a]MnO[sub 3], where Q is selected from the group consisting of Ca and Sr or mixtures thereof and a' is from 0.1 to 0.8, the electrical interconnection comprising Y[sub 1[minus]b]Ca[sub b]Cr[sub 1[minus]c]Al[sub c]O[sub 3], where b' is from 0.1 to 0.6 and c' is from 0.0 to 0.3; a yttrium stabilized solid electrolyte comprising (1[minus]d)ZrO[sub 2]-(d)Y[sub 2]O[sub 3] where d' is from 0.06 to 0.5; and a solid fuel electrode comprising X-ZrO[sub 2], where X' is an elemental metal. 5 figs.

  10. Solid oxide fuel cells, and air electrode and electrical interconnection materials therefor

    DOEpatents

    Bates, J. Lambert

    1992-01-01

    In one aspect of the invention, an air electrode material for a solid oxide fuel cell comprises Y.sub.1-a Q.sub.a MnO.sub.3, where "Q" is selected from the group consisting of Ca and Sr or mixtures thereof and "a" is from 0.1 to 0.8. Preferably, "a" is from 0.4 to 0.7. In another aspect of the invention, an electrical interconnection material for a solid oxide fuel cell comprises Y.sub.1-b Ca.sub.b Cr.sub.1-c Al.sub.c O.sub.3, where "b" is from 0.1 to 0.6 and "c" is from 0 to 9.3. Preferably, "b" is from 0.3 to 0.5 and "c" is from 0.05 to 0.1. A composite solid oxide electrochemical fuel cell incorporating these materials comprises: a solid oxide air electrode and an adjacent solid oxide electrical interconnection which commonly include the cation Y, the air electrode comprising Y.sub.1-a Q.sub.a MnO.sub.3, where "Q" is selected from the group consisting of Ca and Sr or mixtures thereof and "a" is from 0.1 to 0.8, the electrical interconnection comprising Y.sub.1-b Ca.sub.b Cr.sub.1-c Al.sub.c O.sub.3, where "b" is from 0.1 to 0.6 and "c" is from 0.0 to 0.3; a yttrium stabilized solid electrolyte comprising (1-d)ZrO.sub.2 -(d)Y.sub.2 O.sub.3 where "d" is from 0.06 to 0.5; and a solid fuel electrode comprising X-ZrO.sub.2, where "X" is an elemental metal.

  11. Improved zinc electrode and rechargeable zinc-air battery

    DOEpatents

    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.

  12. In Situ-Grown ZnCo2O4 on Single-Walled Carbon Nanotubes as Air Electrode Materials for Rechargeable Lithium-Oxygen Batteries.

    PubMed

    Liu, Bin; Xu, Wu; Yan, Pengfei; Bhattacharya, Priyanka; Cao, Ruiguo; Bowden, Mark E; Engelhard, Mark H; Wang, Chong-Min; Zhang, Ji-Guang

    2015-11-01

    The development of highly efficient catalysts is critical for the practical application of lithium-oxygen (Li-O2) batteries. Nanosheet-assembled ZnCo2O4 (ZCO) microspheres and thin films grown in situ on single-walled carbon nanotube (ZCO/SWCNT) composites as high-performance air electrode materials for Li-O2 batteries are reported. The in situ grown ZCO/SWCNT electrodes delivered high discharge capacities, decreased the onset of the oxygen evolution reaction by 0.9 V during the charging process, and led to longer cycling stability. These results indicate that in situ grown ZCO/SWCNT composites can be used as highly efficient air electrode materials for oxygen reduction and evolution reactions. The enhanced catalytic activity displayed by the uniformly dispersed ZCO catalyst on nanostructured electrodes is expected to inspire further development of other catalyzed electrodes for Li-O2 batteries and other applications. PMID:26457378

  13. In Situ-Grown ZnCo2O4 on Single-Walled Carbon Nanotubes as Air Electrode Materials for Rechargeable Lithium–Oxygen Batteries

    SciTech Connect

    Liu, Bin; Xu, Wu; Yan, Pengfei; Bhattacharya, Priyanka; Cao, Ruiguo; Bowden, Mark E.; Engelhard, Mark H.; Wang, Chong M.; Zhang, Jiguang

    2015-10-12

    Although lithium-oxygen (Li-O2) batteries have great potential to be used as one of the next generation energy storage systems due to their ultrahigh theoretical specific energy, there are still many significant barriers before their practical applications. These barriers include electrolyte and electrode instability, poor ORR/OER efficiency and cycling capability, etc. Development of a highly efficient catalyst will not only enhance ORR/OER efficiency, it may also improve the stability of electrolyte because the reduced charge voltage. Here we report the synthesis of nano-sheet-assembled ZnCo2O4 spheres/single walled carbon nanotubes (ZCO/SWCNTs) composites as high performance air electrode materials for Li-O2 batteries. The ZCO catalyzed SWCNTs electrodes delivered high discharge capacities, decreased the onset of oxygen evolution reaction by 0.9 V during charge processes, and led to more stable cycling stability. These results indicate that ZCO/SWCNTs composite can be used as highly efficient air electrode for oxygen reduction and evolution reactions. The highly enhanced catalytic activity by uniformly dispersed ZnCo2O4 catalyst on nanostructured electrodes is expected to inspire

  14. Development of self-supporting air electrode SOFC

    SciTech Connect

    Nagata, M.; Iwasawa, C.; Yamaoka, S.; Seino, Y.; Ono, M.

    1995-12-31

    The authors are studying a self-supporting SOFC using the spray coating method, etc. A high-performance self-supporting air electrode has successfully been produced by the extrusion-sintering method, and a cell with its electrolyte and fuel electrode manufactured by the plasma spray coating method on the air electrode proved to have good performance. The maximum output density of a single cell is 0.31W/cm{sup 2}. Furthermore, the authors are developing a FGM (Functionally Gradient Material) film as the fuel electrode produced by the plasma spray coating method.

  15. Air plasma jet with hollow electrodes at atmospheric pressure

    SciTech Connect

    Hong, Yong Cheol; Uhm, Han Sup

    2007-05-15

    Atmospheric-pressure plasma jet with air is produced through hollow electrodes and dielectric with a hole of 1 mm diam. The plasma jet device is operated by injecting pressurized air into the electrode hole. The air plasma jet device at average powers less than 5 W exhibits a cold plasma jet of about 2 cm in length and near the room temperature, being low enough to treat thermally sensitive materials. Preliminary studies on the discharge characteristics and application tests are also presented by comparing the air plasma jet with the nitrogen and argon plasma jet.

  16. Redox electrode materials for supercapatteries

    NASA Astrophysics Data System (ADS)

    Yu, Linpo; Chen, George Z.

    2016-09-01

    Redox electrode materials, including transition metal oxides and electronically conducting polymers, are capable of faradaic charge transfer reactions, and play important roles in most electrochemical energy storage devices, such as supercapacitor, battery and supercapattery. Batteries are often based on redox materials with low power capability and safety concerns in some cases. Supercapacitors, particularly those based on redox inactive materials, e.g. activated carbon, can offer high power output, but have relatively low energy capacity. Combining the merits of supercapacitor and battery into a hybrid, the supercapattery can possess energy as much as the battery and output a power almost as high as the supercapacitor. Redox electrode materials are essential in the supercapattery design. However, it is hard to utilise these materials easily because of their intrinsic characteristics, such as the low conductivity of metal oxides and the poor mechanical strength of conducting polymers. This article offers a brief introduction of redox electrode materials, the basics of supercapattery and its relationship with pseudocapacitors, and reviews selectively some recent progresses in the relevant research and development.

  17. Air plasma jet with hollow electrodes at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Hong, Yong Cheol; Uhm, Han Sup

    2007-05-01

    Atmospheric-pressure plasma jet with air is produced through hollow electrodes and dielectric with a hole of 5W exhibits a cold plasma jet of about 2cm in length and near the room temperature, being low enough to treat thermally sensitive materials. Preliminary studies on the discharge characteristics and application tests are also presented by comparing the air plasma jet with the nitrogen and argon plasma jet.

  18. Air electrode composition for solid oxide fuel cell

    DOEpatents

    Kuo, Lewis; Ruka, Roswell J.; Singhal, Subhash C.

    1999-01-01

    An air electrode composition for a solid oxide fuel cell is disclosed. The air electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO.sub.3. The A-site of the air electrode composition comprises a mixed lanthanide in combination with rare earth and alkaline earth dopants. The B-site of the composition comprises Mn in combination with dopants such as Mg, Al, Cr and Ni. The mixed lanthanide comprises La, Ce, Pr and, optionally, Nd. The rare earth A-site dopants preferably comprise La, Nd or a combination thereof, while the alkaline earth A-site dopant preferably comprises Ca. The use of a mixed lanthanide substantially reduces raw material costs in comparison with compositions made from high purity lanthanum starting materials. The amount of the A-site and B-site dopants is controlled in order to provide an air electrode composition having a coefficient of thermal expansion which closely matches that of the other components of the solid oxide fuel cell.

  19. Air electrode composition for solid oxide fuel cell

    DOEpatents

    Kuo, L.; Ruka, R.J.; Singhal, S.C.

    1999-08-03

    An air electrode composition for a solid oxide fuel cell is disclosed. The air electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO{sub 3}. The A-site of the air electrode composition comprises a mixed lanthanide in combination with rare earth and alkaline earth dopants. The B-site of the composition comprises Mn in combination with dopants such as Mg, Al, Cr and Ni. The mixed lanthanide comprises La, Ce, Pr and, optionally, Nd. The rare earth A-site dopants preferably comprise La, Nd or a combination thereof, while the alkaline earth A-site dopant preferably comprises Ca. The use of a mixed lanthanide substantially reduces raw material costs in comparison with compositions made from high purity lanthanum starting materials. The amount of the A-site and B-site dopants is controlled in order to provide an air electrode composition having a coefficient of thermal expansion which closely matches that of the other components of the solid oxide fuel cell. 3 figs.

  20. 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.

  1. Bifunctional air electrodes containing elemental iron powder charging additive

    DOEpatents

    Liu, Chia-tsun; Demczyk, Brian G.; Gongaware, Paul R.

    1982-01-01

    A bifunctional air electrode for use in electrochemical energy cells is made, comprising a hydrophilic layer and a hydrophobic layer, where the hydrophilic layer essentially comprises a hydrophilic composite which includes: (i) carbon; (ii) elemental iron particles having a particle size of between about 25 microns and about 700 microns diameter; (iii) an oxygen evolution material; (iv) a nonwetting agent; and (v) a catalyst, where at least one current collector is formed into said composite.

  2. Advances in electrode materials for AMTEC

    NASA Astrophysics Data System (ADS)

    Ryan, M. A.; Williams, R. M.; Lara, L.; Fiebig, B. G.; Cortez, R. H.; Kisor, A. K.; Shields, V. B.; Homer, M. L.

    2001-02-01

    A mixed conducting electrode for the Alkali Metal Thermal to Electric Converter (AMTEC) has been made and tested. The electrode is made from a slurry of metal and TiO2 powders which is applied to the electrolyte and fired to sinter the electrode material. During the first 48-72 hours of operation in a SETC, the electrode takes up Na from low pressure sodium vapor to make a metal-Na-Ti-O compound. This compound is electronically conducting and ionically conducting to sodium; electronic conduction is also provided by the metal in the electrode. With a mixed conducting electrode made from robust, low vapor pressure materials, the promise for improved performance and lifetime is high. .

  3. LOWER TEMPERATURE ELECTROLYTE AND ELECTRODE MATERIALS

    SciTech Connect

    Keqin Huang

    2003-04-30

    A thorough literature survey on low-temperature electrolyte and electrode materials for SOFC is given in this report. Thermodynamic stability of selected electrolyte and its chemical compatibility with cathode substrate were evaluated. Preliminary electrochemical characterizations were conducted on symmetrical cells consisting of the selected electrolyte and various electrode materials. Feasibility of plasma spraying new electrolyte material thin-film on cathode substrate was explored.

  4. Architecture engineering of supercapacitor electrode materials

    NASA Astrophysics Data System (ADS)

    Chen, Kunfeng; Li, Gong; Xue, Dongfeng

    2016-02-01

    The biggest challenge for today’s supercapacitor systems readily possessing high power density is their low energy density. Their electrode materials with controllable structure, specific surface area, electronic conductivity, and oxidation state, have long been highlighted. Architecture engineering of functional electrode materials toward powerful supercapacitor systems is becoming a big fashion in the community. The construction of ion-accessible tunnel structures can microscopically increase the specific capacitance and materials utilization; stiff 3D structures with high specific surface area can macroscopically assure high specific capacitance. Many exciting findings in electrode materials mainly focus on the construction of ice-folded graphene paper, in situ functionalized graphene, in situ crystallizing colloidal ionic particles and polymorphic metal oxides. This feature paper highlights some recent architecture engineering strategies toward high-energy supercapacitor electrode systems, including electric double-layer capacitance (EDLC) and pseudocapacitance.

  5. Oxide modified air electrode surface for high temperature electrochemical cells

    DOEpatents

    Singh, Prabhakar; Ruka, Roswell J.

    1992-01-01

    An electrochemical cell is made having a porous cermet electrode (16) and a porous lanthanum manganite electrode (14), with solid oxide electrolyte (15) between them, where the lanthanum manganite surface next to the electrolyte contains a thin discontinuous layer of high surface area cerium oxide and/or praseodymium oxide, preferably as discrete particles (30) in contact with the air electrode and electrolyte.

  6. 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.

  7. Reversibly immobilized biological materials in monolayer films on electrodes

    SciTech Connect

    Weaver, P.F.; Frank, A.J.

    1991-04-08

    A method is provided for reversibly binding charged biological particles in a fluid medium to an electrode surface. The method comprises treating (e.g., derivatizing) the electrode surface with an electrochemically active material; connecting the electrode to an electrical potential; and exposing the fluid medium to the electrode surface in a manner such that the charged particles become adsorbed on the electrode surface.

  8. LOWER TEMPERATURE ELECTROLYTE AND ELECTRODE MATERIALS

    SciTech Connect

    Keqin Huang

    2001-04-30

    A thorough literature survey on low-temperature electrolyte and electrode materials for solid oxide fuel cells (SOFC) is presented. Preliminary results of co-sintering LaGaO{sub 3} (LSGM) film on the cathode substrate were also reported. The chemical stability of LSGM in various SOFC environments was thermodynamically assessed and verified by the molten-salt technique.

  9. Gallium Nitride Crystals: Novel Supercapacitor Electrode Materials.

    PubMed

    Wang, Shouzhi; Zhang, Lei; Sun, Changlong; Shao, Yongliang; Wu, Yongzhong; Lv, Jiaxin; Hao, Xiaopeng

    2016-05-01

    A type of single-crystal gallium nitride mesoporous membrane is fabricated and its supercapacitor properties are demonstrated for the first time. The supercapacitors exhibit high-rate capability, stable cycling life at high rates, and ultrahigh power density. This study may expand the range of crystals as high-performance electrode materials in the field of energy storage.

  10. Lanthanum manganite-based air electrode for solid oxide fuel cells

    DOEpatents

    Ruka, Roswell J.; Kuo, Lewis; Li, Baozhen

    1999-01-01

    An air electrode material for a solid oxide fuel cell is disclosed. The electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO.sub.3. The A-site of the air electrode material preferably comprises La, Ca, Ce and at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd. The B-site of the electrode material comprises Mn with substantially no dopants. The ratio of A:B is preferably slightly above 1. A preferred air electrode composition is of the formula La.sub.w Ca.sub.x Ln.sub.y Ce.sub.z MnO.sub.3, wherein Ln comprises at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd, w is from about 0.55 to about 0.56, x is from about 0.255 to about 0.265, y is from about 0.175 to about 0.185, and z is from about 0.005 to about 0.02. The air electrode material possesses advantageous chemical and electrical properties as well as favorable thermal expansion and thermal cycle shrinkage characteristics.

  11. Lanthanum manganite-based air electrode for solid oxide fuel cells

    DOEpatents

    Ruka, R.J.; Kuo, L.; Li, B.

    1999-06-29

    An air electrode material for a solid oxide fuel cell is disclosed. The electrode material is based on lanthanum manganite having a perovskite-like crystal structure ABO[sub 3]. The A-site of the air electrode material preferably comprises La, Ca, Ce and at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd. The B-site of the electrode material comprises Mn with substantially no dopants. The ratio of A:B is preferably slightly above 1. A preferred air electrode composition is of the formula La[sub w]Ca[sub x]Ln[sub y]Ce[sub z]MnO[sub 3], wherein Ln comprises at least one lanthanide selected from Sm, Gd, Dy, Er, Y and Nd, w is from about 0.55 to about 0.56, x is from about 0.255 to about 0.265, y is from about 0.175 to about 0.185, and z is from about 0.005 to about 0.02. The air electrode material possesses advantageous chemical and electrical properties as well as favorable thermal expansion and thermal cycle shrinkage characteristics. 10 figs.

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

    NASA Astrophysics Data System (ADS)

    Chellapandi Velraj, Samgopiraj

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

  13. 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.

  14. 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.

  15. Vanadium based materials as electrode materials for high performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Yan, Yan; Li, Bing; Guo, Wei; Pang, Huan; Xue, Huaiguo

    2016-10-01

    As a kind of supercapacitors, pseudocapacitors have attracted wide attention in recent years. The capacitance of the electrochemical capacitors based on pseudocapacitance arises mainly from redox reactions between electrolytes and active materials. These materials usually have several oxidation states for oxidation and reduction. Many research teams have focused on the development of an alternative material for electrochemical capacitors. Many transition metal oxides have been shown to be suitable as electrode materials of electrochemical capacitors. Among them, vanadium based materials are being developed for this purpose. Vanadium based materials are known as one of the best active materials for high power/energy density electrochemical capacitors due to its outstanding specific capacitance and long cycle life, high conductivity and good electrochemical reversibility. There are different kinds of synthetic methods such as sol-gel hydrothermal/solvothermal method, template method, electrospinning method, atomic layer deposition, and electrodeposition method that have been successfully applied to prepare vanadium based electrode materials. In our review, we give an overall summary and evaluation of the recent progress in the research of vanadium based materials for electrochemical capacitors that include synthesis methods, the electrochemical performances of the electrode materials and the devices.

  16. 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.

  17. 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.

  18. 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

  19. Screening of redox couples and electrode materials

    NASA Technical Reports Server (NTRS)

    Giner, J.; Swette, L.; Cahill, K.

    1976-01-01

    Electrochemical parameters of selected redox couples that might be potentially promising for application in bulk energy storage systems were investigated. This was carried out in two phases: a broad investigation of the basic characteristics and behavior of various redox couples, followed by a more limited investigation of their electrochemical performance in a redox flow reactor configuration. In the first phase of the program, eight redox couples were evaluated under a variety of conditions in terms of their exchange current densities as measured by the rotating disk electrode procedure. The second phase of the program involved the testing of four couples in a redox reactor under flow conditions with a varity of electrode materials and structures.

  20. Improving Electrode Durability of PEF Chamber by selecting suitable material

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Corrosion resistance of four materials - titanium, platinized titanium, stainless steel, and boron carbide - as electrodes in a Pulsed Electric Field (PEF) system was studied to reduce electrode material migration into the food by electrode corrosion. The PEF process conditions were 28 kV/cm field s...

  1. Conductor-polymer composite electrode materials

    DOEpatents

    Ginley, D.S.; Kurtz, S.R.; Smyrl, W.H.; Zeigler, J.M.

    1984-06-13

    A conductive composite material useful as an electrode, comprises a conductor and an organic polymer which is reversibly electrochemically dopable to change its electrical conductivity. Said polymer continuously surrounds the conductor in intimate electrical contact therewith and is prepared by electrochemical growth on said conductor or by reaction of its corresponding monomer(s) on said conductor which has been pre-impregnated or pre-coated with an activator for said polymerization. Amount of the conductor is sufficient to render the resultant composite electrically conductive even when the polymer is in an undoped insulating state.

  2. 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.

  3. Carbon-based electrode materials for DNA electroanalysis.

    PubMed

    Kato, Dai; Niwa, Osamu

    2013-01-01

    This review addresses recent studies of newly developed carbon-based electrode materials and their use for DNA electroanalysis. Recently, new carbon materials including carbon nanotubes (CNT), graphene and diamond-based nanocarbon electrodes have been actively developed as sensing platforms for biomolecules, such as DNA and proteins. Electrochemical techniques using these new material-based electrodes can provide very simple and inexpensive sensing platforms, and so are expected to be used as one of the "post-light" DNA analysis methods, which include coulometric detection, amperometric detection with electroactive tags or intercalators, and potentiometric detection. DNA electroanalysis using these new carbon materials is summarized in view of recent advances on electrodes.

  4. Extrusion of electrode material by liquid injection into extruder barrel

    DOEpatents

    Keller, D.G.; Giovannoni, R.T.; MacFadden, K.O.

    1998-03-10

    An electrode sheet product is formed using an extruder having a feed throat and a downstream section by separately mixing an active electrode material and a solid polymer electrolyte composition that contains lithium salt. The active electrode material is fed into the feed throat of the extruder, while a portion of at least one fluid component of the solid polymer electrolyte composition is introduced to the downstream section. The active electrode material and the solid polymer electrolyte composition are compounded in a downstream end of the extruder. The extruded sheets, adhered to current collectors, can be formed into battery cells. 1 fig.

  5. Extrusion of electrode material by liquid injection into extruder barrel

    DOEpatents

    Keller, David Gerard; Giovannoni, Richard Thomas; MacFadden, Kenneth Orville

    1998-01-01

    An electrode sheet product is formed using an extruder having a feed throat and a downstream section by separately mixing an active electrode material and a solid polymer electrolyte composition that contains lithium salt. The active electrode material is fed into the feed throat of the extruder, while a portion of at least one fluid component of the solid polymer electrolyte composition is introduced to the downstream section. The active electrode material and the solid polymer electrolyte composition are compounded in a downstream end of the extruder. The extruded sheets, adhered to current collectors, can be formed into battery cells.

  6. Aqueous processing of composite lithium ion electrode material

    DOEpatents

    Li, Jianlin; Armstrong, Beth L; Daniel, Claus; Wood, III, David L

    2015-02-17

    A method of making a battery electrode includes the steps of dispersing an active electrode material and a conductive additive in water with at least one dispersant to create a mixed dispersion; treating a surface of a current collector to raise the surface energy of the surface to at least the surface tension of the mixed dispersion; depositing the dispersed active electrode material and conductive additive on a current collector; and heating the coated surface to remove water from the coating.

  7. Multi-walled carbon nanotubes as electrode material for microbial fuel cells.

    PubMed

    Thepsuparungsikul, N; Phonthamachai, N; Ng, H Y

    2012-01-01

    The microbial fuel cell (MFC) is a novel and innovative technology that could allow direct harvesting of energy from wastewater through microbial activity with simultaneous oxidation of organic matter in wastewater. Among all MFC parts, electrode materials play a crucial role in electricity generation. A variety of electrode materials have been used, including plain graphite, carbon paper and carbon cloth. However, these electrode materials generated only limited electricity or power. Recently, many research studies have been conducted on carbon nanotubes (CNTs) because of their unique physical and chemical properties that include high conductivity, high surface area, corrosion resistance, and electrochemical stability. These properties make them extremely attractive for fabricating electrodes and catalyst supports. In this study, CNT-based electrodes had been developed to improve MFC performance in terms of electricity generation and treatment efficiency. Multi-walled carbon nanotubes (MWCNTs) with carboxyl groups have been employed to fabricate electrodes for single-chamber air-cathode MFCs. The quality of the prepared MWCNTs-based electrodes was evaluated by morphology, electrical conductivity and specific surface area using a field emission scanning electron microscope, four-probe method and Brunauer-Emmerr-Teller method, respectively. The performance of MFCs equipped with MWCNT-based electrodes was evaluated by chemical analysis and electrical monitoring and calculation. In addition, the performance of these MFCs, using MWCNTs as electrodes, was compared against that using commercial carbon cloth.

  8. Multi-walled carbon nanotubes as electrode material for microbial fuel cells.

    PubMed

    Thepsuparungsikul, N; Phonthamachai, N; Ng, H Y

    2012-01-01

    The microbial fuel cell (MFC) is a novel and innovative technology that could allow direct harvesting of energy from wastewater through microbial activity with simultaneous oxidation of organic matter in wastewater. Among all MFC parts, electrode materials play a crucial role in electricity generation. A variety of electrode materials have been used, including plain graphite, carbon paper and carbon cloth. However, these electrode materials generated only limited electricity or power. Recently, many research studies have been conducted on carbon nanotubes (CNTs) because of their unique physical and chemical properties that include high conductivity, high surface area, corrosion resistance, and electrochemical stability. These properties make them extremely attractive for fabricating electrodes and catalyst supports. In this study, CNT-based electrodes had been developed to improve MFC performance in terms of electricity generation and treatment efficiency. Multi-walled carbon nanotubes (MWCNTs) with carboxyl groups have been employed to fabricate electrodes for single-chamber air-cathode MFCs. The quality of the prepared MWCNTs-based electrodes was evaluated by morphology, electrical conductivity and specific surface area using a field emission scanning electron microscope, four-probe method and Brunauer-Emmerr-Teller method, respectively. The performance of MFCs equipped with MWCNT-based electrodes was evaluated by chemical analysis and electrical monitoring and calculation. In addition, the performance of these MFCs, using MWCNTs as electrodes, was compared against that using commercial carbon cloth. PMID:22437017

  9. Reversibly immobilized biological materials in monolayer films on electrodes

    SciTech Connect

    Weaver, Paul F.; Frank, Arthur J.

    1993-01-01

    Methods and techniques are described for reversibly binding charged biological particles in a fluid medium to an electrode surface. The methods are useful in a variety of applications. The biological materials may include microbes, proteins, and viruses. The electrode surface may consist of reversibly electroactive materials such as polyvinylferrocene, silicon-linked ferrocene or quinone.

  10. Reversibly immobilized biological materials in monolayer films on electrodes

    DOEpatents

    Weaver, P.F.; Frank, A.J.

    1993-05-04

    Methods and techniques are described for reversibly binding charged biological particles in a fluid medium to an electrode surface. The methods are useful in a variety of applications. The biological materials may include microbes, proteins, and viruses. The electrode surface may consist of reversibly electroactive materials such as polyvinylferrocene, silicon-linked ferrocene or quinone.

  11. Materials analyses and electrochemical impedance of implantable metal electrodes.

    PubMed

    Howlader, Matiar M R; Ul Alam, Arif; Sharma, Rahul P; Deen, M Jamal

    2015-04-21

    Implantable electrodes with high flexibility, high mechanical fixation and low electrochemical impedance are desirable for neuromuscular activation because they provide safe, effective and stable stimulation. In this paper, we report on detailed materials and electrical analyses of three metal implantable electrodes - gold (Au), platinum (Pt) and titanium (Ti) - using X-ray photoelectron spectroscopy (XPS), scanning acoustic microscopy, drop shape analysis and electrochemical impedance spectroscopy. We investigated the cause of changes in electrochemical impedance of long-term immersed Au, Pt and Ti electrodes on liquid crystal polymers (LCPs) in phosphate buffered saline (PBS). We analyzed the surface wettability, surface and interface defects and the elemental depth profile of the electrode-adhesion layers on the LCP. The impedance of the electrodes decreased at lower frequencies, but increased at higher frequencies compared with that of the short-term immersion. The increase of impedances was influenced by the oxidation of the electrode/adhesion-layers that affected the double layer capacitance behavior of the electrode/PBS. The oxidation of the adhesion layer for all the electrodes was confirmed by XPS. Alkali ions (sodium) were adsorbed on the Au and Pt surfaces, but diffused into the Ti electrode and LCPs. The Pt electrode showed a higher sensitivity to surface and interface defects than that of Ti and Au electrodes. These findings may be useful when designing electrodes for long-term implantable devices.

  12. Modified lithium vanadium oxide electrode materials products and methods

    DOEpatents

    Thackeray, Michael M.; Kahaian, Arthur J.; Visser, Donald R.; Dees, Dennis W.; Benedek, Roy

    1999-12-21

    A method of improving certain vanadium oxide formulations is presented. The method concerns fluorine doping formulations having a nominal formula of LiV.sub.3 O.sub.8. Preferred average formulations are provided wherein the average oxidation state of the vanadium is at least 4.6. Herein preferred fluorine doped vanadium oxide materials, electrodes using such materials, and batteries including at least one electrode therein comprising such materials are provided.

  13. 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.

  14. 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.

  15. 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.

  16. Recirculating electric air filter

    DOEpatents

    Bergman, W.

    1985-01-09

    An electric air filter cartridge has a cylindrical inner high voltage electrode, a layer of filter material, and an outer ground electrode formed of a plurality of segments moveably connected together. The outer electrode can be easily opened to remove or insert filter material. Air flows through the two electrodes and the filter material and is exhausted from the center of the inner electrode.

  17. Post-test evaluation of the oxygen electrode from a solid oxide electrolysis stack and electrode materials development.

    SciTech Connect

    Mawdsley, J. R.; Carter, J. D.; Yildiz, B.; Call, A. V.; Kropf, A. J.; Ferrandon, M. S.; Myers, D. J.; Maroni, V. A.

    2009-05-01

    The conclusions of this paper are: (1) stack degradation analysis - significant sources of degradation have been identified, (a) oxygen electrode delamination off the electrolyte and (b) chromium contamination of the oxygen electrode and bond layer; (2) electrode materials development - improved electrode materials have been demonstrated, Pr{sub 2}NiO{sub 4} oxygen electrodes show state-of-the-art performance without optimization of fabrication parameters.

  18. Fuel cell electrode interconnect contact material encapsulation and method

    DOEpatents

    Derose, Anthony J.; Haltiner, Jr., Karl J.; Gudyka, Russell A.; Bonadies, Joseph V.; Silvis, Thomas W.

    2016-05-31

    A fuel cell stack includes a plurality of fuel cell cassettes each including a fuel cell with an anode and a cathode. Each fuel cell cassette also includes an electrode interconnect adjacent to the anode or the cathode for providing electrical communication between an adjacent fuel cell cassette and the anode or the cathode. The interconnect includes a plurality of electrode interconnect protrusions defining a flow passage along the anode or the cathode for communicating oxidant or fuel to the anode or the cathode. An electrically conductive material is disposed between at least one of the electrode interconnect protrusions and the anode or the cathode in order to provide a stable electrical contact between the electrode interconnect and the anode or cathode. An encapsulating arrangement segregates the electrically conductive material from the flow passage thereby, preventing volatilization of the electrically conductive material in use of the fuel cell stack.

  19. Effect of oxidation of carbon material on suspension electrodes for flow electrode capacitive deionization.

    PubMed

    Hatzell, Kelsey B; Hatzell, Marta C; Cook, Kevin M; Boota, Muhammad; Housel, Gabrielle M; McBride, Alexander; Kumbur, E Caglan; Gogotsi, Yury

    2015-03-01

    Flow electrode deionization (FCDI) is an emerging area for continuous and scalable deionization, but the electrochemical and flow properties of the flow electrode need to be improved to minimize energy consumption. Chemical oxidation of granular activated carbon (AC) was examined here to study the role of surface heteroatoms on rheology and electrochemical performance of a flow electrode (carbon slurry) for deionization processes. Moreover, it was demonstrated that higher mass densities could be used without increasing energy for pumping when using oxidized active material. High mass-loaded flow electrodes (28% carbon content) based on oxidized AC displayed similar viscosities (∼21 Pa s) to lower mass-loaded flow electrodes (20% carbon content) based on nonoxidized AC. The 40% increased mass loading (from 20% to 28%) resulted in a 25% increase in flow electrode gravimetric capacitance (from 65 to 83 F g(-1)) without sacrificing flowability (viscosity). The electrical energy required to remove ∼18% of the ions (desalt) from of the feed solution was observed to be significantly dependent on the mass loading and decreased (∼60%) from 92 ± 7 to 28 ± 2.7 J with increased mass densities from 5 to 23 wt %. It is shown that the surface chemistry of the active material in a flow electrode effects the electrical and pumping energy requirements of a FCDI system.

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

    DOE PAGES

    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

  1. Electrode materials for coal-fired MHD generators

    NASA Astrophysics Data System (ADS)

    Perkins, R. A.

    1980-10-01

    Metallic materials are evaluated as electrodes for coal fired MHD generators. A laboratory test that simulates the electrochemical and corrosive environment was developed and used to characterize electrode behavior in a diffuse current flow (nonarcing) mode of operation. High current density requires that an electron transport mechanism of current flow be maintained. With inert, stable electrodes, anode polarization occurs and ionic conduction prevails, limiting current to low values. The nature of this behavior and approaches to overcoming anodic polarization are studied as a function of electrode material, slag composition, and temperature. By operating at high temperatures and with controlled slag chemistries to produce a very fluid slag, depolarization may be achieved by mechanical mixing. Interrupted current flow are required to aid in breaking down anodic polarization.

  2. Recent advances in material science for developing enzyme electrodes.

    PubMed

    Sarma, Anil Kumar; Vatsyayan, Preety; Goswami, Pranab; Minteer, Shelley D

    2009-04-15

    The enzyme-modified electrode is the fundamental component of amperometric biosensors and biofuel cells. The selection of appropriate combinations of materials, such as: enzyme, electron transport mediator, binding and encapsulation materials, conductive support matrix and solid support, for construction of enzyme-modified electrodes governs the efficiency of the electrodes in terms of electron transfer kinetics, mass transport, stability, and reproducibility. This review investigates the varieties of materials that can be used for these purposes. Recent innovation in conductive electro-active polymers, functionalized polymers, biocompatible composite materials, composites of transition metal-based complexes and organometallic compounds, sol-gel and hydro-gel materials, nanomaterials, other nano-metal composites, and nano-metal oxides are reviewed and discussed here. In addition, the critical issues related to the construction of enzyme electrodes and their application for biosensor and biofuel cell applications are also highlighted in this article. Effort has been made to cover the recent literature on the advancement of materials sciences to develop enzyme electrodes and their potential applications for the construction of biosensors and biofuel cells.

  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. Graphene oxide - Polyvinyl alcohol nanocomposite based electrode material for supercapacitors

    NASA Astrophysics Data System (ADS)

    Pawar, Pranav Bhagwan; Shukla, Shobha; Saxena, Sumit

    2016-07-01

    Supercapacitors are high capacitive energy storage devices and find applications where rapid bursts of power are required. Thus materials offering high specific capacitance are of fundamental interest in development of these electrochemical devices. Graphene oxide based nanocomposites are mechanically robust and have interesting electronic properties. These form potential electrode materials efficient for charge storage in supercapacitors. In this perspective, we investigate low cost graphene oxide based nanocomposites as electrode material for supercapacitor. Nanocomposites of graphene oxide and polyvinyl alcohol were synthesized in solution phase by integrating graphene oxide as filler in polyvinyl alcohol matrix. Structural and optical characterizations suggest the formation of graphene oxide and polyvinyl alcohol nanocomposites. These nanocomposites were found to have high specific capacitance, were cyclable, ecofriendly and economical. Our studies suggest that nanocomposites prepared by adding 0.5% wt/wt of graphene oxide in polyvinyl alcohol can be used an efficient electrode material for supercapacitors.

  5. 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.

  6. Electrode materials and lithium battery systems

    DOEpatents

    Amine, Khalil; Belharouak, Ilias; Liu, Jun

    2011-06-28

    A material comprising a lithium titanate comprising a plurality of primary particles and secondary particles, wherein the average primary particle size is about 1 nm to about 500 nm and the average secondary particle size is about 1 .mu.m to about 4 .mu.m. In some embodiments the lithium titanate is carbon-coated. Also provided are methods of preparing lithium titanates, and devices using such materials.

  7. New electrode materials for dielectric elastomer actuators

    NASA Astrophysics Data System (ADS)

    Yuan, Wei; Lam, Tuling; Biggs, James; Hu, Liangbing; Yu, Zhibin; Ha, Soonmok; Xi, Dongjuan; Senesky, Matthew K.; Grüner, George; Pei, Qibing

    2007-04-01

    Dielectric elastomer actuators exert strain due to an applied electric field. With advantageous properties such as high efficiency and their light weight, these actuators are attractive for a variety of applications ranging from biomimetic robots, medical prosthetics to conventional pumps and valves. The performance and reliability however, are limited by dielectric breakdown which occurs primarily from localized defects inherently present in the polymer film during actuation. These defects lead to electric arcing, causing a short circuit that shuts down the entire actuator and can lead to actuator failure at fields significantly lower than the intrinsic strength of the material. This limitation is particularly a problem in actuators using large-area films. Our recent studies have shown that the gap between the strength of the intrinsic material and the strength of large-area actuators can be reduced by electrically isolating defects in the dielectric film. As a result, the performance and reliability of dielectric elastomers actuators can be substantially improved.

  8. Recirculating electric air filter

    DOEpatents

    Bergman, Werner

    1986-01-01

    An electric air filter cartridge has a cylindrical inner high voltage eleode, a layer of filter material, and an outer ground electrode formed of a plurality of segments moveably connected together. The outer electrode can be easily opened to remove or insert filter material. Air flows through the two electrodes and the filter material and is exhausted from the center of the inner electrode.

  9. Conductive Carbon Coatings for Electrode Materials

    SciTech Connect

    Doeff, Marca M.; Kostecki, Robert; Wilcox, James; Lau, Grace

    2007-07-13

    A simple method for optimizing the carbon coatings on non-conductive battery cathode material powders has been developed at Lawrence Berkeley National Laboratory. The enhancement of the electronic conductivity of carbon coating enables minimization of the amount of carbon in the composites, allowing improvements in battery rate capability without compromising energy density. The invention is applicable to LiFePO{sub 4} and other cathode materials used in lithium ion or lithium metal batteries for high power applications such as power tools and hybrid or plug-in hybrid electric vehicles. The market for lithium ion batteries in consumer applications is currently $5 billion/year. Additionally, lithium ion battery sales for vehicular applications are projected to capture 5% of the hybrid and electric vehicle market by 2010, and 36% by 2015 (http://www.greencarcongress.com). LiFePO{sub 4} suffers from low intrinsic rate capability, which has been ascribed to the low electronic conductivity (10{sup -9} S cm{sup -1}). One of the most promising approaches to overcome this problem is the addition of conductive carbon. Co-synthesis methods are generally the most practical route for carbon coating particles. At the relatively low temperatures (<800 C) required to make LiFePO{sub 4}, however, only poorly conductive disordered carbons are produced from organic precursors. Thus, the carbon content has to be high to produce the desired enhancement in rate capability, which decreases the cathode energy density.

  10. 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.

  11. Electrode material comprising graphene-composite materials in a graphite network

    DOEpatents

    Kung, Harold H.; Lee, Jung K.

    2014-07-15

    A durable electrode material suitable for use in Li ion batteries is provided. The material is comprised of a continuous network of graphite regions integrated with, and in good electrical contact with a composite comprising graphene sheets and an electrically active material, such as silicon, wherein the electrically active material is dispersed between, and supported by, the graphene sheets.

  12. 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.

  13. Highly Conductive, Air-Stable Silver Nanowire@Iongel Composite Films toward Flexible Transparent Electrodes.

    PubMed

    Xiong, Weiwei; Liu, Hongliang; Chen, Yongzhen; Zheng, Meiling; Zhao, Yuanyuan; Kong, Xiangbin; Wang, Ying; Zhang, Xiqi; Kong, Xiangyu; Wang, Pengfei; Jiang, Lei

    2016-09-01

    A new type of flexible transparent electrode is designed, by employing wettability-induced selective electroless-welding of silver nanowire (AgNW) networks, together with a thin conductive iongel as the protective layer. The obtained electrode exhibits high optical transmittance, and excellent air-stability without sacrificing conductivity. PMID:27296551

  14. Method for making carbon super capacitor electrode materials

    DOEpatents

    Firsich, D.W.; Ingersoll, D.; Delnick, F.M.

    1998-07-07

    A method is described for making near-net-shape, monolithic carbon electrodes for energy storage devices. The method includes the controlled pyrolysis and activation of a pressed shape of methyl cellulose powder with pyrolysis being carried out in two stages; pre-oxidation, preferably in air at a temperature between 200--250 C, followed by carbonization under an inert atmosphere. An activation step to adjust the surface area of the carbon shape to a value desirable for the application being considered, including heating the carbon shape in an oxidizing atmosphere to a temperature of at least 300 C, follows carbonization. 1 fig.

  15. Method for making carbon super capacitor electrode materials

    DOEpatents

    Firsich, David W.; Ingersoll, David; Delnick, Frank M.

    1998-01-01

    A method for making near-net-shape, monolithic carbon electrodes for energy storage devices. The method includes the controlled pyrolysis and activation of a pressed shape of methyl cellulose powder with pyrolysis being carried out in two stages; pre-oxidation, preferably in air at a temperature between 200.degree.-250.degree. C., followed by carbonization under an inert atmosphere. An activation step to adjust the surface area of the carbon shape to a value desirable for the application being considered, including heating the carbon shape in an oxidizing atmosphere to a temperature of at least 300.degree. C., follows carbonization.

  16. 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.

  17. Methods for making lithium vanadium oxide electrode materials

    DOEpatents

    Schutts, Scott M.; Kinney, Robert J.

    2000-01-01

    A method of making vanadium oxide formulations is presented. In one method of preparing lithium vanadium oxide for use as an electrode material, the method involves: admixing a particulate form of a lithium compound and a particulate form of a vanadium compound; jet milling the particulate admixture of the lithium and vanadium compounds; and heating the jet milled particulate admixture at a temperature below the melting temperature of the admixture to form lithium vanadium oxide.

  18. Material for electrodes of low temperature plasma generators

    DOEpatents

    Caplan, Malcolm; Vinogradov, Sergel Evge'evich; Ribin, Valeri Vasil'evich; Shekalov, Valentin Ivanovich; Rutberg, Philip Grigor'evich; Safronov, Alexi Anatol'evich

    2008-12-09

    Material for electrodes of low temperature plasma generators. The material contains a porous metal matrix impregnated with a material emitting electrons. The material uses a mixture of copper and iron powders as a porous metal matrix and a Group IIIB metal component such as Y.sub.2O.sub.3 is used as a material emitting electrons at, for example, the proportion of the components, mass %: iron: 3-30; Y.sub.2O.sub.3:0.05-1; copper: the remainder. Copper provides a high level of heat conduction and electric conductance, iron decreases intensity of copper evaporation in the process of plasma creation providing increased strength and lifetime, Y.sub.2O.sub.3 provides decreasing of electronic work function and stability of arc burning. The material can be used for producing the electrodes of low temperature AC plasma generators used for destruction of liquid organic wastes, medical wastes, and municipal wastes as well as for decontamination of low level radioactive waste, the destruction of chemical weapons, warfare toxic agents, etc.

  19. Material for electrodes of low temperature plasma generators

    DOEpatents

    Caplan, Malcolm; Vinogradov, Sergel Evge'evich; Ribin, Valeri Vasil'evich; Shekalov, Valentin Ivanovich; Rutberg, Philip Grigor'evich; Safronov, Alexi Anatol'evich; Shiryaev, Vasili Nikolaevich

    2010-03-02

    Material for electrodes of low temperature plasma generators. The material contains a porous metal matrix impregnated with a material emitting electrons. The material uses a mixture of copper and iron powders as a porous metal matrix and a Group IIIB metal component such as Y.sub.2O.sub.3 is used as a material emitting electrons at, for example, the proportion of the components, mass %: iron:3-30; Y.sub.2O.sub.3:0.05-1; copper: the remainder. Copper provides a high level of heat conduction and electric conductance, iron decreases intensity of copper evaporation in the process of plasma creation providing increased strength and lifetime, Y.sub.2O.sub.3 provides decreasing of electronic work function and stability of arc burning. The material can be used for producing the electrodes of low temperature AC plasma generators used for destruction of liquid organic wastes, medical wastes, municipal wastes as well as for decontamination of low level radioactive waste, the destruction of chemical weapons, warfare toxic agents, etc.

  20. High performance lithium insertion negative electrode materials for electrochemical devices

    NASA Astrophysics Data System (ADS)

    Channu, V. S. Reddy; Rambabu, B.; Kumari, Kusum; Kalluru, Rajmohan R.; Holze, Rudolf

    2016-11-01

    Spinel LiCrTiO4 oxides to be used as electrode materials for a lithium ion battery and an asymmetric supercapacitor were synthesized using a soft-chemical method with and without chelating agents followed by calcination at 700 °C for 10 h. Structural and morphological properties were studied with powder X-ray diffraction, scanning electron and transmission electron microscopy. Particles of 50-10 nm in size are observed in the microscopic images. The presence of Cr and Ti is confirmed from the EDS spectrum. Electrochemical properties of LiCrTiO4 electrode were examined in a lithium ion battery. The electrode prepared with oxalic acid-assisted LiCrTiO4 shows higher specific capacity.This LiCrTiO4 is also used as anode material for an asymmetric hybrid supercapacitor. The cell exhibits a specific capacity of 65 mAh/g at 1 mA/cm2. The specific capacity decreases with increasing current densities.

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

    NASA Astrophysics Data System (ADS)

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

    2014-09-01

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

  2. Iridium oxide-polymer nanocomposite electrode materials for water oxidation.

    PubMed

    Lattach, Youssef; Rivera, Juan Francisco; Bamine, Tahya; Deronzier, Alain; Moutet, Jean-Claude

    2014-08-13

    Nanocomposite anode materials for water oxidation have been readily synthesized by electrodeposition of iridium oxide nanoparticles into poly(pyrrole-alkylammonium) films, previously deposited onto carbon electrodes by oxidative electropolymerization of a pyrrole-alkylammonium monomer. The nanocomposite films were characterized by electrochemistry, transmission electron microscopy, and atomic force microscopy. They showed an efficient electrocatalytic activity toward the oxygen evolution reaction. Data from Tafel plots have demonstrated that the catalytic activity of the iridium oxide nanoparticles is maintained following their inclusion in the polymer matrix. Bulk electrolysis of water at carbon foam modified electrodes have shown that the iridium oxide-polymer composite presents a higher catalytic activity and a better operational stability than regular oxide films.

  3. Spiral configuration of electrodes and dielectric material for sensing an environmental property

    NASA Technical Reports Server (NTRS)

    Laue, Eric G. (Inventor); Stephens, James B. (Inventor)

    1989-01-01

    A reliable moisture-indicating capactive sensor is provided with wire electrodes at least one of which includes a coating of moisture-absorbing dielectric material by spirally twisting the wire electrodes about each other, thereby establishing a pair of electrodes in contact with opposite surfaces of a layer of dielectric material, and assuring consistent contact of each electrode with the dielectric material despite changes in environmental conditions.

  4. Anodes - Materials for negative electrodes in electrochemical energy technology

    NASA Astrophysics Data System (ADS)

    Holze, Rudolf

    2014-06-01

    The basic concepts of electrodes and electrochemical cells (including both galvanic and electrolytic ones) are introduced and illustrated with practical examples. Particular attention is paid to negative electrodes in primary and secondary cells, fuel cell electrodes and electrodes in redox flow batteries. General features and arguments pertaining to selection, optimization and further development are highlighted.

  5. A study of the glow discharge characteristics of contact electrodes at atmospheric pressure in air

    SciTech Connect

    Liu, Wenzheng Sun, Guangliang Li, Chuanhui; Zhang, Rongrong

    2014-04-15

    Electric field distributions and discharge properties of rod-rod contact electrodes were studied under the condition of DBD for the steady generation of atmospheric pressure glow discharge plasma (APGD) in air. We found that under the effect of the initial electrons generated in a nanometer-scale gap, the rod-rod cross-contact electrodes yielded APGD plasma in air. Regarding the rod-rod cross-contact electrodes, increasing the working voltage expanded the strong electric field area of the gas gap so that both discharge area and discharge power increased, and the increase in the number of contact points kept the initial discharge voltage unchanged and caused an increase in the plasma discharge area and discharge power. A mesh-like structure of cross-contact electrodes was designed and used to generate more APGD plasma, suggesting high applicability.

  6. Electrode electrolyte interlayers containing cerium oxide for electrochemical fuel cells

    DOEpatents

    Borglum, Brian P.; Bessette, Norman F.

    2000-01-01

    An electrochemical cell is made having a porous fuel electrode (16) and a porous air electrode (13), with solid oxide electrolyte (15) therebetween, where the air electrode surface opposing the electrolyte has a separate, attached, dense, continuous layer (14) of a material containing cerium oxide, and where electrolyte (16) contacts the continuous oxide layer (14), without contacting the air electrode (13).

  7. A novel carbon electrode material for highly improved EDLC performance.

    PubMed

    Fang, Baizeng; Binder, Leo

    2006-04-20

    Porous materials, developed by grafting functional groups through chemical surface modification with a surfactant, represent an innovative concept in energy storage. This work reports, in detail, the first practical realization of a novel carbon electrode based on grafting of vinyltrimethoxysilane (vtmos) functional group for energy storage in electric double layer capacitor (EDLC). Surface modification with surfactant vtmos enhances the hydrophobisation of activated carbon and the affinity toward propylene carbonate (PC) solvent, which improves the wettability of activated carbon in the electrolyte solution based on PC solvent, resulting in not only a lower resistance to the transport of electrolyte ions within micropores of activated carbon but also more usable surface area for the formation of electric double layer, and accordingly, higher specific capacitance, energy density, and power capability available from the capacitor based on modified carbon. Especially, the effects from surface modification become superior at higher discharge rate, at which much better EDLC performance (i.e., much higher energy density and power capability) has been achieved by the modified carbon, suggesting that the modified carbon is a novel and very promising electrode material of EDLC for large current applications where both high energy density and power capability are required. PMID:16610885

  8. 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).

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

    NASA Astrophysics Data System (ADS)

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

    2010-02-01

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

  10. 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

  11. Novel materials for negative electrodes in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Pereira, Nathalie

    Carbonaceous materials are currently utilized as negative electrodes in commercial rechargeable Li-ion batteries. However, their low capacity prompted the search for alternative materials of higher capacity and good cycling stability in order to maximize the battery energy density and cycle life. Lithium alloys have long been considered as alternative negative electrode materials to substitute for the carbonaceous materials currently used in commercial rechargeable Li-ion batteries. However, they suffer from cracking caused by the large volume changes occurring during lithiation and delithiation. To better understand the alloys failure mechanism, various elements were tested and those that can alloy with lithium electrochemically were identified. Silicon showed extremely high capacity but poor cycle life. To investigate to which extent multiphase materials may improve cycle life, several binary metal-silicides were explored in search for improved cycling stability. Mg 2Si was the only compound of high capacity but it exhibited poor cycle life. Both addition of a matrix and decrease in particle size have been demonstrated to improve cycle life. Each effect has been investigated separately. Using tin-based powders of different size oxidized to various extent, we showed an increase in oxygen content, a particle size decrease and the formation of converted Sn-Sb compounds improved cycling stability. The effect of the matrix nature on the electrochemical properties was explored using Zn-based conversion materials. Upon reaction with lithium, ZnO and ZnS electrodes generated LiZn and a Li2O and Li2S matrix, respectively. The reversible process was identified as the Li-Zn alloying reaction, as obtained in pure metallic Zn electrodes. ZnO and ZnS failure mechanisms were also similar to metallic Zn. However, ZnS showed improved cycle life. LiZnN has been isolated by way of an electrochemical conversion reaction of Zn3N2 with lithium. We showed Zn3N 2 reversibly reacts with

  12. Application of infrared spectroscopy to monitoring gas insulated high-voltage equipment: electrode material-dependent SF(6) decomposition.

    PubMed

    Kurte, R; Beyer, C; Heise, H M; Klockow, D

    2002-08-01

    Sulfur hexafluoride is a chemically inert gas which is used in gas insulated substations (GIS) and other high-voltage equipment, leading to a significant enhancement of apparatus lifetime and reductions in installation size and maintenance requirements compared to conventional air insulated substations. However, component failures due to aging of the gas through electrical discharges may occur, and on-site monitoring for risk assessment is needed. Infrared spectroscopy was used for the analysis of gaseous by-products generated from electrical discharges in sulfur hexafluoride gas. An infrared monitoring system was developed using a micro-cell coupled to an FTIR spectrometer by silver halide fibers. Partial least-squares calibration was applied by using a limited number of optimally selected spectral variables. Emphasis was placed on the determination of main decomposition products, such as SOF(2), SOF(4), and SO(2)F(2). Besides the different electrical conditions, the material of the plane counter electrode of the discharge chamber was also varied between silver, aluminum, copper, tungsten, or tungsten/copper alloy. For the spark experiments the point electrode was the same material as chosen for the plane electrode, whereas for partial discharges a stainless steel needle was employed. Complementary investigations on the chemical composition within the solid counter electrode material by secondary neutral mass spectrometry (SNMS) were also carried out. Under sparking conditions, the electrode material plays an important role in the decomposition rates of the gas-phase, but no relevant material dependence could be observed under partial discharge conditions. PMID:12185577

  13. 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.

  14. Characteristics of radio-frequency, atmospheric-pressure glow discharges with air using bare metal electrodes

    SciTech Connect

    Wang Huabo; Sun Wenting; Li Heping; Bao Chengyu; Zhang Xiaozhang

    2006-10-16

    In this letter, an induced gas discharge approach is proposed and described in detail for obtaining a uniform atmospheric-pressure glow discharge with air in a {gamma} mode using water-cooled, bare metal electrodes driven by radio-frequency (13.56 MHz) power supply. A preliminary study on the discharge characteristics of the air glow discharge is also presented in this study. With this induced gas discharge approach, radio-frequency, atmospheric-pressure glow discharges using bare metal electrodes with other gases which cannot be ignited directly as the plasma working gas, such as nitrogen, oxygen, etc., can also be obtained.

  15. 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.

  16. Nanostructured Mo-based electrode materials for electrochemical energy storage.

    PubMed

    Hu, Xianluo; Zhang, Wei; Liu, Xiaoxiao; Mei, Yueni; Huang, Yunhui

    2015-04-21

    The development of advanced energy storage devices is at the forefront of research geared towards a sustainable future. Nanostructured materials are advantageous in offering huge surface to volume ratios, favorable transport features, and attractive physicochemical properties. They have been extensively explored in various fields of energy storage and conversion. This review is focused largely on the recent progress in nanostructured Mo-based electrode materials including molybdenum oxides (MoO(x), 2 ≤ x ≤ 3), dichalconides (MoX2, X = S, Se), and oxysalts for rechargeable lithium/sodium-ion batteries, Mg batteries, and supercapacitors. Mo-based compounds including MoO2, MoO3, MoO(3-y) (0 < y < 1), MMo(x)O(y) (M = Fe, Co, Ni, Ca, Mn, Zn, Mg, or Cd; x = 1, y = 4; x = 3, y = 8), MoS2, MoSe2, (MoO2)2P2O7, LiMoO2, Li2MoO3, etc. possess multiple valence states and exhibit rich chemistry. They are very attractive candidates for efficient electrochemical energy storage systems because of their unique physicochemical properties, such as conductivity, mechanical and thermal stability, and cyclability. In this review, we aim to provide a systematic summary of the synthesis, modification, and electrochemical performance of nanostructured Mo-based compounds, as well as their energy storage applications in lithium/sodium-ion batteries, Mg batteries, and pseudocapacitors. The relationship between nanoarchitectures and electrochemical performances as well as the related charge-storage mechanism is discussed. Moreover, remarks on the challenges and perspectives of Mo-containing compounds for further development in electrochemical energy storage applications are proposed. This review sheds light on the sustainable development of advanced rechargeable batteries and supercapacitors with nanostructured Mo-based electrode materials.

  17. Work function determination of promising electrode materials for thermionic converters

    NASA Technical Reports Server (NTRS)

    Jacobson, D.

    1977-01-01

    Work performed on this contract was primarily for the evaluation of selected electrode materials for thermionic energy converters. The original objective was to characterize selected nickel based superalloys up to temperatures of 1400 K. It was found that an early selection, Inconel 800 produced a high vapor pressure which interfered with the vacuum emission measurements. The program then shifted to two other areas. The first area was to obtain emission from the superalloys in a cesiated atmosphere. The cesium plasma helps to suppress the vaporization interference. The second area involved characterization of the Lanthanum-Boron series as thermionic emitters. These final two areas resulted in three journal publications which are attached to this report.

  18. 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.

  19. High valence transition metal doped strontium ferrites for electrode materials in symmetrical SOFCs

    NASA Astrophysics Data System (ADS)

    Fernández-Ropero, A. J.; Porras-Vázquez, J. M.; Cabeza, A.; Slater, P. R.; Marrero-López, D.; Losilla, E. R.

    2014-03-01

    In this paper we report the successful incorporation of high valence transition metals, i.e. Cr, Mo, W, V, Nb, Ti, Zr into SrFeO3-δ perovskite materials, for potential applications as symmetric electrode materials for Solid Oxide Fuel Cells. It is observed that the doping leads to a change from an orthorhombic structure (with partial ordering of oxygen vacancies) to a cubic one (with the oxygen vacancies disordered). These electrodes are chemically compatibles with Ce0.9Gd0.1O1.95 (CGO) and La0.8Sr0.2Ga0.8Mg0.2O3-δ (LSGM) electrolytes at least up to 1100 °C. Thermal annealing experiments in 5% H2-Ar at 800 °C also show the stability of the doped samples in reducing conditions, suggesting that they may be suitable for both cathode and anode applications. In contrast, reduction of undoped SrFeO3-δ leads to the observation of extra peaks indicating the formation of the brownmillerite structure with the associated oxygen vacancy ordering. The performance of these electrodes was examined on dense electrolyte pellets of CGO and LSGM in air and 5% H2-Ar. In both atmospheres an improvement in the area specific resistances (ASR) values is observed for the doped samples with respect to the parent compound. Thus, the results show that high valence transition metals can be incorporated into SrFeO3-δ-based materials and can have a beneficial effect on the electrochemical performance, making them potentially suitable for use as cathode and anode materials in symmetrical SOFC.

  20. Characteristics of a nanosecond discharge in atmospheric air with a liquid electrolytic electrode

    NASA Astrophysics Data System (ADS)

    Shuaibov, A. K.; Shevera, I. V.; Kozak, Ya. Yu.; Kentesh, G. V.

    2014-06-01

    The spatial, electric, and radiative characteristics of a pulse-periodic nanosecond discharge between an electrode based on a system of blades and the distilled water surface as well as an aqueous solution of zinc sulfate in atmospheric air are considered.

  1. 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.

  2. 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.

  3. 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.

  4. SOFC chromite sintering and electrolyte/air-electrode interface reactions

    SciTech Connect

    Bates, J.L.; Chick, L.A.; Youngblood, G.E.

    1992-04-01

    Air sintering of chromites was investigated in La(Sr)CrO[sub 3], La(Ca)CrO[sub 3], and Y(Ca)CrO[sub 3]. Effects of alkaline earth dopant level and chromium enrichment/depletion on chromite sintered densities and microstructures are discussed. Ac impedance spectroscopy and dc polarization coupled with an unbonded interface cell were used to examine SOFC (solid oxide fuel cells) electrochemical reactions at solid-solid-gas interfaces, particularly for La[sub 1-x]Sr[sub x]MnO[sub 3]. 5 refs.

  5. SOFC chromite sintering and electrolyte/air-electrode interface reactions

    SciTech Connect

    Bates, J.L.; Chick, L.A.; Youngblood, G.E.

    1992-04-01

    Air sintering of chromites was investigated in La(Sr)CrO{sub 3}, La(Ca)CrO{sub 3}, and Y(Ca)CrO{sub 3}. Effects of alkaline earth dopant level and chromium enrichment/depletion on chromite sintered densities and microstructures are discussed. Ac impedance spectroscopy and dc polarization coupled with an unbonded interface cell were used to examine SOFC (solid oxide fuel cells) electrochemical reactions at solid-solid-gas interfaces, particularly for La{sub 1-x}Sr{sub x}MnO{sub 3}. 5 refs.

  6. 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

  7. Effects of atmospheric air plasma treatment of graphite and carbon felt electrodes on the anodic current from Shewanella attached cells.

    PubMed

    Epifanio, Monica; Inguva, Saikumar; Kitching, Michael; Mosnier, Jean-Paul; Marsili, Enrico

    2015-12-01

    The attachment of electrochemically active microorganisms (EAM) on an electrode is determined by both the chemistry and topography of the electrode surface. Pre-treatment of the electrode surface by atmospheric air plasma introduces hydrophilic functional groups, thereby increasing cell attachment and electroactivity in short-term experiments. In this study, we use graphite and carbon felt electrodes to grow the model EAM Shewanella loihica PV-4 at oxidative potential (0.2 V vs. Ag/AgCl). Cell attachment and electroactivity are measured through electrodynamic methods. Atmospheric air plasma pre-treatment increases cell attachment and current output at graphite electrodes by 25%, while it improves the electroactivity of the carbon felt electrodes by 450%. Air plasma pre-treatment decreased the coulombic efficiency on both carbon felt and graphite electrodes by 60% and 80%, respectively. Microbially produced flavins adsorb preferentially at the graphite electrode, and air plasma pre-treatment results in lower flavin adsorption at both graphite and carbon felt electrodes. Results show that air plasma pre-treatment is a feasible option to increase current output in bioelectrochemical systems.

  8. Effects of Electrode Material on the Voltage of a Tree-Based Energy Generator

    PubMed Central

    2015-01-01

    The voltage between a standing tree and its surrounding soil is regarded as an innovative renewable energy source. This source is expected to provide a new power generation system for the low-power electrical equipment used in forestry. However, the voltage is weak, which has caused great difficulty in application. Consequently, the development of a method to increase the voltage is a key issue that must be addressed in this area of applied research. As the front-end component for energy harvesting, a metal electrode has a material effect on the level and stability of the voltage obtained. This study aimed to preliminarily ascertain the rules and mechanisms that underlie the effects of electrode material on voltage. Electrodes of different materials were used to measure the tree-source voltage, and the data were employed in a comparative analysis. The results indicate that the conductivity of the metal electrode significantly affects the contact resistance of the electrode-soil and electrode-trunk contact surfaces, thereby influencing the voltage level. The metal reactivity of the electrode has no significant effect on the voltage. However, passivation of the electrode materials markedly reduces the voltage. Suitable electrode materials are demonstrated and recommended. PMID:26302491

  9. Monte Carlo modelling the dosimetric effects of electrode material on diamond detectors.

    PubMed

    Baluti, Florentina; Deloar, Hossain M; Lansley, Stuart P; Meyer, Juergen

    2015-03-01

    Diamond detectors for radiation dosimetry were modelled using the EGSnrc Monte Carlo code to investigate the influence of electrode material and detector orientation on the absorbed dose. The small dimensions of the electrode/diamond/electrode detector structure required very thin voxels and the use of non-standard DOSXYZnrc Monte Carlo model parameters. The interface phenomena was investigated by simulating a 6 MV beam and detectors with different electrode materials, namely Al, Ag, Cu and Au, with thickens of 0.1 µm for the electrodes and 0.1 mm for the diamond, in both perpendicular and parallel detector orientation with regards to the incident beam. The smallest perturbations were observed for the parallel detector orientation and Al electrodes (Z = 13). In summary, EGSnrc Monte Carlo code is well suited for modelling small detector geometries. The Monte Carlo model developed is a useful tool to investigate the dosimetric effects caused by different electrode materials. To minimise perturbations cause by the detector electrodes, it is recommended that the electrodes should be made from a low-atomic number material and placed parallel to the beam direction.

  10. 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.

  11. CMOS compatible electrode materials selection in oxide-based memory devices

    NASA Astrophysics Data System (ADS)

    Zhuo, V. Y.-Q.; Li, M.; Guo, Y.; Wang, W.; Yang, Y.; Jiang, Y.; Robertson, J.

    2016-07-01

    Electrode materials selection guidelines for oxide-based memory devices are constructed from the combined knowledge of observed device operation characteristics, ab-initio calculations, and nano-material characterization. It is demonstrated that changing the top electrode material from Ge to Cr to Ta in the Ta2O5-based memory devices resulted in a reduction of the operation voltages and current. Energy Dispersed X-ray (EDX) Spectrometer analysis clearly shows that the different top electrode materials scavenge oxygen ions from the Ta2O5 memory layer at various degrees, leading to different oxygen vacancy concentrations within the Ta2O5, thus the observed trends in the device performance. Replacing the Pt bottom electrode material with CMOS compatible materials (Ru and Ir) further reduces the power consumption and can be attributed to the modification of the Schottky barrier height and oxygen vacancy concentration at the electrode/oxide interface. Both trends in the device performance and EDX results are corroborated by the ab-initio calculations which reveal that the electrode material tunes the oxygen vacancy concentration via the oxygen chemical potential and defect formation energy. This experimental-theoretical approach strongly suggests that the proper selection of CMOS compatible electrode materials will create the critical oxygen vacancy concentration to attain low power memory performance.

  12. Surface and interface engineering of electrode materials for lithium-ion batteries.

    PubMed

    Wang, Kai-Xue; Li, Xin-Hao; Chen, Jie-Sheng

    2015-01-21

    Lithium-ion batteries are regarded as promising energy storage devices for next-generation electric and hybrid electric vehicles. In order to meet the demands of electric vehicles, considerable efforts have been devoted to the development of advanced electrode materials for lithium-ion batteries with high energy and power densities. Although significant progress has been recently made in the development of novel electrode materials, some critical issues comprising low electronic conductivity, low ionic diffusion efficiency, and large structural variation have to be addressed before the practical application of these materials. Surface and interface engineering is essential to improve the electrochemical performance of electrode materials for lithium-ion batteries. This article reviews the recent progress in surface and interface engineering of electrode materials including the increase in contact interface by decreasing the particle size or introducing porous or hierarchical structures and surface modification or functionalization by metal nanoparticles, metal oxides, carbon materials, polymers, and other ionic and electronic conductive species.

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

    NASA Astrophysics Data System (ADS)

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

    2016-09-01

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

  14. Metallic sulfide additives for positive electrode material within a secondary electrochemical cell

    DOEpatents

    Walsh, William J.; McPheeters, Charles C.; Yao, Neng-ping; Koura, Kobuyuki

    1976-01-01

    An improved active material for use within the positive electrode of a secondary electrochemical cell includes a mixture of iron disulfide and a sulfide of a polyvalent metal. Various metal sulfides, particularly sulfides of cobalt, nickel, copper, cerium and manganese, are added in minor weight proportion in respect to iron disulfide for improving the electrode performance and reducing current collector requirements.

  15. Method for determining trace quantities of chloride in polymeric materials using ion selective electrodes: Final report

    SciTech Connect

    Salary, J.

    1987-02-01

    A method for determining trace quantities of chloride in polymeric materials has been developed. Ion-selective electrodes and the standard addition method were used in all the analyses. The ion-selective electrode method was compared with neutron activation, ion chromatography and chloridometer titration. The ion-selective electrode technique results for chloride were similar to those of neutron activation, which is the acknowledged referee method. This ion-selective electrode method showed the highest standard recovery when compared with the ion chromatography and chloridometer titration methods.

  16. Air electrode material for high temperature electrochemical cells

    DOEpatents

    Ruka, Roswell J.

    1985-01-01

    Disclosed is a solid solution with a perovskite-like crystal structure having the general formula La.sub.1-x-w (M.sub.L).sub.x (Ce).sub.w (M.sub.S1).sub.1-y (M.sub.S2).sub.y O.sub.3 where M.sub.L is Ca, Sr, Ba, or mixtures thereof, M.sub.S1 is Mn, Cr, or mixtures thereof and M.sub.S2 is Ni, Fe, Co, Ti, Al, In, Sn, Mg, Y, Nb, Ta, or mixtures thereof, w is about 0.05 to about 0.25, x+w is about 0.1 to about 0.7, and y is 0 to about 0.5. In the formula, M.sub.L is preferably Ca, w is preferably 0.1 to 0.2, x+w is preferably 0.4 to 0.7, and y is preferably 0. The solid solution can be used in an electrochemical cell where it more closely matches the thermal expansion characteristics of the support tube and electrolyte of the cell.

  17. 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

  18. 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.

  19. A comparison of two rocket borne Langmuir probes having electrodes of different materials

    NASA Technical Reports Server (NTRS)

    Schutz, S. R.; Smith, L. G.

    1975-01-01

    The behavior of two types of Langmuir probes, one with electrodes made of low-sulfur stainless steel and one with electrodes made of aluminum coated with Aquadag, has been compared on two rocket flights. Each rocket payload included one Langmuir probe of each type. The electron temperatures measured with the stainless-steel electrodes were about 15% higher than the electron temperatures measured with the Aquadag-coated electrodes at 150 km on ascent and about 10% higher at 180 km. These results imply that the use of Aquadag coated electrodes or electrodes of other carefully chosen materials permits greater reliability in the measurement of electron temperatures in the ionosphere by the Langmuir probe technique.

  20. Electrochemical degradation of trichloroacetic acid in aqueous media: influence of the electrode material.

    PubMed

    Esclapez, M D; Díez-García, M I; Sàez, V; Bonete, P; González-García, José

    2013-01-01

    The electrochemical degradation of trichloroacetic acid (TCAA) in water has been analysed through voltammetric studies with a rotating disc electrode and controlled-potential bulk electrolyses. The influence of the mass-transport conditions and initial concentration of TCAA for titanium, stainless steel and carbon electrodes has been studied. It is shown that the electrochemical reduction of TCAA takes place prior to the massive hydrogen evolution in the potential window for all electrode materials studied. The current efficiency is high (> 18%) compared with those normally reported in the literature, and the fractional conversion is above 50% for all the electrodes studied. Only dichloroacetic acid (DCAA) and chloride anions were routinely detected as reduction products for any of the electrodes, and reasonable values of mass balance error were obtained. Of the three materials studied, the titanium cathode gave the best results. PMID:23530352

  1. Method for producing electrodes using microscale or nanoscale materials obtained from hydrogendriven metallurgical reactions

    DOEpatents

    Reilly, James J.; Adzic, Gordana D.; Johnson, John R.; Vogt, Thomas; McBreen, James

    2003-09-02

    A method is provided for producing electrodes using microscale and nanoscale metal materials formed from hydrogen driven metallurgical processes; such a the HD (hydriding, dehydriding) process, the HDDR (hydriding, dehydriding, disproportionation, and recombination) process, and variants thereof.

  2. 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.

  3. A Metal-Free, Free-Standing, Macroporous Graphene@g-C₃N₄ Composite Air Electrode for High-Energy Lithium Oxygen Batteries.

    PubMed

    Luo, Wen-Bin; Chou, Shu-Lei; Wang, Jia-Zhao; Zhai, Yu-Chun; Liu, Hua-Kun

    2015-06-01

    The nonaqueous lithium oxygen battery is a promising candidate as a next-generation energy storage system because of its potentially high energy density (up to 2-3 kW kg(-1)), exceeding that of any other existing energy storage system for storing sustainable and clean energy to reduce greenhouse gas emissions and the consumption of nonrenewable fossil fuels. To achieve high energy density, long cycling stability, and low cost, the air electrode structure and the electrocatalysts play important roles. Here, a metal-free, free-standing macroporous graphene@graphitic carbon nitride (g-C3N4) composite air cathode is first reported, in which the g-C3N4 nanosheets can act as efficient electrocatalysts, and the macroporous graphene nanosheets can provide space for Li2O2 to deposit and also promote the electron transfer. The electrochemical results on the graphene@g-C3N4 composite air electrode show a 0.48 V lower charging plateau and a 0.13 V higher discharging plateau than those of pure graphene air electrode, with a discharge capacity of nearly 17300 mA h g(-1)(composite) . Excellent cycling performance, with terminal voltage higher than 2.4 V after 105 cycles at 1000 mA h g(-1)(composite) capacity, can also be achieved. Therefore, this hybrid material is a promising candidate for use as a high energy, long-cycle-life, and low-cost cathode material for lithium oxygen batteries.

  4. 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.

  5. Production and study of megawatt air-nitrogen plasmatron with divergent channel of an output electrode

    NASA Astrophysics Data System (ADS)

    Isakaev, E. H.; Chinnov, V. F.; Tyuftyaev, A. S.; Gadzhiev, M. Kh; Sargsyan, M. A.; Konovalov, P. V.

    2015-11-01

    Megawatt generator of high-enthalpy air plasma jet (H ≥ 30 kJ/g) is constructed. Plasmatron belongs to the class of plasma torches with thermionic cathode, tangential swirl flow and divergent channel of an output electrode-anode. Plasma torch ensures the formation of the slightly divergent (2α = 12°) air plasma jet with the diameter D = 50 mm. The current-voltage characteristics of the plasma torch has virtually unchanged voltage relative to its current with enhanced (compared with arcs in cylindrical channels) stable combustion zone. Preliminary analysis of the obtained air plasma spectra shows that at a current of 1500 A near-axis zone of the plasma jet is characterized by a temperature of up to 15000 K, and the peripheral radiating area has a temperature of 8000-9000 K.

  6. Design rules for electrode arrangement in an air-breathing alkaline direct methanol laminar flow fuel cell

    NASA Astrophysics Data System (ADS)

    Thorson, Michael R.; Brushett, Fikile R.; Timberg, Chris J.; Kenis, Paul J. A.

    2012-11-01

    The influence of electrode length on performance is investigated in an air-breathing alkaline direct methanol laminar flow fuel cell (LFFC). Depletion of methanol at the electrode surface along the direction of flow hinders reaction kinetics and consequently also cell performance. Reducing the electrode length can decrease the influence of boundary layer depletion, and thereby, improve both the current and power densities. Here, the effect of boundary layer depletion was found to play a significant effect on performance within the first 18 mm of an electrode length. To further utilize the increased power densities provided by shorter electrode lengths, alternative electrode aspect ratios (electrode length-to-width) and electrode arrangements were explored experimentally. Furthermore, by fitting an empirical model based on experimentally obtained data, we demonstrate that a configuration comprised of a series of short electrodes and operated at low flow rates can achieve higher current and power outputs. The analysis of optimal electrode aspect ratio and electrode arrangements can also be applied to other microfluidic reactor designs in which reaction depletion boundary layers occur due to surface reactions.

  7. The differing behavior of electrosurgical devices made of various electrode materials operating under plasma conditions

    NASA Astrophysics Data System (ADS)

    Stalder, K. R.; Ryan, T. P.; Gaspredes, J.; Woloszko, J.

    2015-03-01

    Coblation® is an electrosurgical technology which employs electrically-excited electrodes in the presence of saline solution to produce a localized and ionized plasma that can cut, ablate, and otherwise treat tissues for many different surgical needs. To improve our understanding of how Coblation plasmas develop from devices made from different electrode materials we describe several experiments designed to elucidate material effects. Initial experiments studied simple, noncommercial cylindrical electrode test devices operating in buffered isotonic saline without applied suction. The applied RF voltage, approximately 300 V RMS, was sufficient to form glow discharges around the active electrodes. The devices exhibited significantly different operating characteristics, which we ascribe to the differing oxidation tendencies and other physical properties of the electrode materials. Parameters measured include RMS voltage and current, instantaneous voltage and current, temporally-resolved light emission and optical emission spectra, and electrode mass-loss measurements. We correlate these measured properties with some of the bulk characteristics of the electrode materials such as work functions, standard reduction potentials and sputter yields.

  8. Direct laser immobilization of photosynthetic material on screen printed electrodes for amperometric biosensor

    SciTech Connect

    Boutopoulos, Christos; Zergioti, Ioanna; Touloupakis, Eleftherios; Pezzotti, Ittalo; Giardi, Maria Teresa

    2011-02-28

    This letter demonstrates the direct laser printing of photosynthetic material onto low cost nonfunctionalized screen printed electrodes for the fabrication of photosynthesis-based amperometric biosensors. The high kinetic energy of the transferred material induces direct immobilization of the thylakoids onto the electrodes without the use of linkers. This type of immobilization is able to establish efficient electrochemical contact between proteins and electrode, stabilizing the photosynthetic biomolecule and transporting electrons to the solid state device with high efficiency. The functionality of the laser printed biosensors was evaluated by the detection of a common herbicide such as Linuron.

  9. Effect of top electrode material on radiation-induced degradation of ferroelectric thin film structures

    NASA Astrophysics Data System (ADS)

    Brewer, Steven J.; Deng, Carmen Z.; Callaway, Connor P.; Paul, McKinley K.; Fisher, Kenzie J.; Guerrier, Jonathon E.; Rudy, Ryan Q.; Polcawich, Ronald G.; Jones, Jacob L.; Glaser, Evan R.; Cress, Cory D.; Bassiri-Gharb, Nazanin

    2016-07-01

    The effects of gamma irradiation on the dielectric and piezoelectric responses of Pb[Zr0.52Ti0.48]O3 (PZT) thin film stacks were investigated for structures with conductive oxide (IrO2) and metallic (Pt) top electrodes. The samples showed, generally, degradation of various key dielectric, ferroelectric, and electromechanical responses when exposed to 2.5 Mrad (Si) 60Co gamma radiation. However, the low-field, relative dielectric permittivity, ɛr, remained largely unaffected by irradiation in samples with both types of electrodes. Samples with Pt top electrodes showed substantial degradation of the remanent polarization and overall piezoelectric response, as well as pinching of the polarization hysteresis curves and creation of multiple peaks in the permittivity-electric field curves post irradiation. The samples with oxide electrodes, however, were largely impervious to the same radiation dose, with less than 5% change in any of the functional characteristics. The results suggest a radiation-induced change in the defect population or defect energy in PZT with metallic top electrodes, which substantially affects motion of internal interfaces such as domain walls. Additionally, the differences observed for stacks with different electrode materials implicate the ferroelectric-electrode interface as either the predominant source of radiation-induced effects (Pt electrodes) or the site of healing for radiation-induced defects (IrO2 electrodes).

  10. Chemical and physical characterization of electrode materials of spent sealed Ni-Cd batteries.

    PubMed

    Nogueira, C A; Margarido, F

    2007-01-01

    The present work aimed at the chemical and physical characterization of spent sealed MONO-type Ni-Cd batteries, contributing to a better definition of the recycling process of these spent products. The electrode material containing essentially nickel, cadmium and some cobalt corresponds to approximately 49% of the weight of the batteries. The remaining components are the steel parts from the external case and the supporting grids (40%) containing Fe and Ni, the electrolyte (9%) and the plastic components (2%). Elemental quantitative analysis showed that the electrodes are highly concentrated in metals. The phase identification achieved by X-ray powder diffraction combined with chemical analysis and leaching tests allowed the authors to proceed with the composition of the electrode materials as following: cathode: 28.7% metallic Ni, 53.3% Ni(OH)2, 6.8% Cd(OH)2 and 2.8% Co(OH)2; anode: 39.4% metallic Ni and 57.0% Cd(OH)2. The morphology of the electrodes was studied by microscopic techniques and two phases were observed in the electrodes: (1) a bright metallic phase constituted of small nickel grains that acts as conductor, and (2) the main hydroxide phase of the active electrodes into which the nickel grains are dispersed. The disaggregation of the electrode particles from the supporting plates was easily obtained during the dismantling procedures, indicating that a substantial percentage of the electrodes can be efficiently separated by wet sieving after shredding the spent batteries.

  11. Chemical and physical characterization of electrode materials of spent sealed Ni-Cd batteries.

    PubMed

    Nogueira, C A; Margarido, F

    2007-01-01

    The present work aimed at the chemical and physical characterization of spent sealed MONO-type Ni-Cd batteries, contributing to a better definition of the recycling process of these spent products. The electrode material containing essentially nickel, cadmium and some cobalt corresponds to approximately 49% of the weight of the batteries. The remaining components are the steel parts from the external case and the supporting grids (40%) containing Fe and Ni, the electrolyte (9%) and the plastic components (2%). Elemental quantitative analysis showed that the electrodes are highly concentrated in metals. The phase identification achieved by X-ray powder diffraction combined with chemical analysis and leaching tests allowed the authors to proceed with the composition of the electrode materials as following: cathode: 28.7% metallic Ni, 53.3% Ni(OH)2, 6.8% Cd(OH)2 and 2.8% Co(OH)2; anode: 39.4% metallic Ni and 57.0% Cd(OH)2. The morphology of the electrodes was studied by microscopic techniques and two phases were observed in the electrodes: (1) a bright metallic phase constituted of small nickel grains that acts as conductor, and (2) the main hydroxide phase of the active electrodes into which the nickel grains are dispersed. The disaggregation of the electrode particles from the supporting plates was easily obtained during the dismantling procedures, indicating that a substantial percentage of the electrodes can be efficiently separated by wet sieving after shredding the spent batteries. PMID:17166709

  12. Germanium as negative electrode material for sodium-ion batteries

    SciTech Connect

    Baggetto, Loic; Keum, Jong Kahk; Browning, Jim; Veith, Gabriel M

    2013-01-01

    Germanium electrodes show a reversible Na-ion reaction at potentials of 0.15 and 0.6 V during discharge and charge, respectively. The reaction is accompanied with a reversible capacity close to 350 mAh g-1, which matches the value expected for the formation of NaGe. The electrode capacity retention is stable over 15 cycles but declines somewhat rapidly afterwards. This decline is typical for alloying systems undergoing large volume expansion, and calls for engineering solutions to confine the mechanical stress and control the electrolyte decomposition reactions that are likely to be the main sources of degradations. The rate performance results highlight the huge potential of nanosized germanium as a potential Na-ion anode. The reaction kinetics is found to be very good with about 220 mAh g-1 delivered at 170 C. Finally, the preliminary XRD results do not reveal the formation of crystalline phases at full (dis)charge.

  13. Making Li-air batteries rechargeable: material challenges

    SciTech Connect

    Shao, Yuyan; Ding, Fei; Xiao, Jie; Zhang, Jian; Xu, Wu; Park, Seh Kyu; Zhang, Jiguang; Wang, Yong; Liu, Jun

    2013-02-25

    A Li-air battery could potentially provide three to five times higher energy density/specific energy than conventional batteries, thus enable the driving range of an electric vehicle comparable to a gasoline vehicle. However, making Li-air batteries rechargeable presents significant challenges, mostly related with materials. Herein, we discuss the key factors that influence the rechargeability of Li-air batteries with a focus on nonaqueous system. The status and materials challenges for nonaqueous rechargeable Li-air batteries are reviewed. These include electrolytes, cathode (electocatalysts), lithium metal anodes, and oxygen-selective membranes (oxygen supply from air). The perspective of rechargeable Li-air batteries is provided.

  14. Unconventional supercapacitors from nanocarbon-based electrode materials to device configurations.

    PubMed

    Liu, Lili; Niu, Zhiqiang; Chen, Jun

    2016-07-25

    As energy storage devices, supercapacitors that are also called electrochemical capacitors possess high power density, excellent reversibility and long cycle life. The recent boom in electronic devices with different functions in transparent LED displays, stretchable electronic systems and artificial skin has increased the demand for supercapacitors to move towards light, thin, integrated macro- and micro-devices with transparent, flexible, stretchable, compressible and/or wearable abilities. The successful fabrication of such supercapacitors depends mainly on the preparation of innovative electrode materials and the design of unconventional supercapacitor configurations. Tremendous research efforts have been recently made to design and construct innovative nanocarbon-based electrode materials and supercapacitors with unconventional configurations. We review here recent developments in supercapacitors from nanocarbon-based electrode materials to device configurations. The advances in nanocarbon-based electrode materials mainly include the assembly technologies of macroscopic nanostructured electrodes with different dimensions of carbon nanotubes/nanofibers, graphene, mesoporous carbon, activated carbon, and their composites. The electrodes with macroscopic nanostructured carbon-based materials overcome the issues of low conductivity, poor mechanical properties, and limited dimensions that are faced by conventional methods. The configurational design of advanced supercapacitor devices is presented with six types of unconventional supercapacitor devices: flexible, micro-, stretchable, compressible, transparent and fiber supercapacitors. Such supercapacitors display unique configurations and excellent electrochemical performance at different states such as bending, stretching, compressing and/or folding. For example, all-solid-state simplified supercapacitors that are based on nanostructured graphene composite paper are able to maintain 95% of the original capacity at

  15. Unconventional supercapacitors from nanocarbon-based electrode materials to device configurations.

    PubMed

    Liu, Lili; Niu, Zhiqiang; Chen, Jun

    2016-07-25

    As energy storage devices, supercapacitors that are also called electrochemical capacitors possess high power density, excellent reversibility and long cycle life. The recent boom in electronic devices with different functions in transparent LED displays, stretchable electronic systems and artificial skin has increased the demand for supercapacitors to move towards light, thin, integrated macro- and micro-devices with transparent, flexible, stretchable, compressible and/or wearable abilities. The successful fabrication of such supercapacitors depends mainly on the preparation of innovative electrode materials and the design of unconventional supercapacitor configurations. Tremendous research efforts have been recently made to design and construct innovative nanocarbon-based electrode materials and supercapacitors with unconventional configurations. We review here recent developments in supercapacitors from nanocarbon-based electrode materials to device configurations. The advances in nanocarbon-based electrode materials mainly include the assembly technologies of macroscopic nanostructured electrodes with different dimensions of carbon nanotubes/nanofibers, graphene, mesoporous carbon, activated carbon, and their composites. The electrodes with macroscopic nanostructured carbon-based materials overcome the issues of low conductivity, poor mechanical properties, and limited dimensions that are faced by conventional methods. The configurational design of advanced supercapacitor devices is presented with six types of unconventional supercapacitor devices: flexible, micro-, stretchable, compressible, transparent and fiber supercapacitors. Such supercapacitors display unique configurations and excellent electrochemical performance at different states such as bending, stretching, compressing and/or folding. For example, all-solid-state simplified supercapacitors that are based on nanostructured graphene composite paper are able to maintain 95% of the original capacity at

  16. Compliant Electrode and Composite Material for Piezoelectric Wind and Mechanical Energy Conversions

    NASA Technical Reports Server (NTRS)

    Chen, Bin (Inventor)

    2015-01-01

    A thin film device for harvesting energy from wind. The thin film device includes one or more layers of a compliant piezoelectric material formed from a composite of a polymer and an inorganic material, such as a ceramic. Electrodes are disposed on a first side and a second side of the piezoelectric material. The electrodes are formed from a compliant material, such as carbon nanotubes or graphene. The thin film device exhibits improved resistance to structural fatigue upon application of large strains and repeated cyclic loadings.

  17. The Science of Electrode Materials for Lithium Batteries - Progress Report

    SciTech Connect

    Brent Fultz

    2003-08-15

    OAK-B135 (IPLD Cleared) Basic materials science research on materials for anodes and cathodes in electrochemical cells. The work is a mix of electrochemical measurements and analysis of the materials by transmission electron microscopy and x-ray diffractometry. The emphasis is on the thermodynamics and kinetics of how lithium is intercalated and de-intercalleted into anode and cathod materials.

  18. Porous hollow carbon spheres for electrode material of supercapacitors and support material of dendritic Pt electrocatalyst

    NASA Astrophysics Data System (ADS)

    Fan, Yang; Liu, Pei-Fang; Huang, Zhong-Yuan; Jiang, Tong-Wu; Yao, Kai-Li; Han, Ran

    2015-04-01

    Porous hollow carbon spheres (PHCSs) are prepared through hydrothermal carbonization of alginic acid and subsequent chemical activation by KOH. The porosity of the alginic acid derived PHCSs can be finely modulated by varying activation temperature in the range of 600-900 °C. The PHCSs activated at 900 °C possess the largest specific surface area (2421 m2 g-1), well-balanced micro- and mesoporosity, as well as high content of oxygen-containing functional groups. As the electrode material for supercapacitors, the PHCSs exhibit superior capacitive performance with specific capacitance of 314 F g-1 at current density of 1 A g-1. Pt nanodendrites supported on the PHCSs are synthesized by polyol reduction method which exhibit high electrocatalytic activity towards methanol oxidation reaction (MOR). Moreover, CO-poisoning tolerance of the Pt nanodendrites is greatly enhanced owing to the surface chemical property of the PHCSs support.

  19. 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.

  20. Understanding the influence of the electrode material on microbial fuel cell performance

    NASA Astrophysics Data System (ADS)

    Sanchez, David V. P.

    In this thesis, I deploy sets of electrodes into microbial fuel cells (MFC), characterize their performance, and evaluate the influence of both platinum catalysts and carbon-based electrodes on current production. The platinum work centers on improving current production by optimizing the use of the catalyst using nano-fabrication techniques. The carbon-electrode work seeks to determine the influence of the bare electrode on biofilm-anode current production. The development of electrodes for MFCs has boomed over the past decade, however, experiments aimed at identifying how catalyst deposition methods and electrode properties influence current production have been limited. The research conducted here is an attempt to expand this knowledge base for platinum catalysts and carbon electrodes. In the initial chapters (4 and 5), I discuss our attempt to decrease catalyst loadings while increasing current production through the use of platinum nanoparticles. The results demonstrate that incorporating platinum nanoparticles throughout the anode and cathode is an efficient means of increasing MFC current production relative to surface deposition because it increases catalyst surface area. The later chapters (chapters 6 and 7) develop an understanding of the importance of electrode properties (i.e. surface area, activation resistance, conductivity, surface morphology) by electrochemically evaluating well-studied anode-respiring pure cultures on different carbon electrode architectures. Two different architectures are produced by using tubular and platelet shaped constituent materials (i.e. carbon fibers and graphene nanoplatelets) and the morphologies of the electrodes are varied by altering the size of the constituent material. The electrodes are characterized and evaluated in MFCs using either Shewanella oneidensis MR-1 or Geobacter sulfurreducens as the innoculant because their bioelectrochemical physiologies are the most documented in the literature. Using the

  1. Characterization of desalination performance of CDI electrode materials using extended electroimpedance spectroscopy

    NASA Astrophysics Data System (ADS)

    Rios Perez, Carlos; Wilkes, Ellen; Hidrovo, Carlos

    2015-11-01

    A comprehensive characterization of porous materials developed for capacitive deionization (CDI) electrodes is very important for the future of this desalination technology. Traditional methods assess the adsorption performance of the electrodes using gas adsorption techniques and electrochemical tests. However, these results fail at comparing quantitatively the performance of different electrode materials. This presentation proposes using a combination of extended electroimpedance spectroscopy (EIS) tests and BET analysis to appraise the amount of salt adsorbed in a flow-by CDI system. The extended EIS experiments were analyzed using an equivalent circuit with three characteristic tiers that represent the dominant ionic migration processes with different time-scales: electro adsorption of ions in the micropores, migration of ion from bulk solution through macropores, adsorption of ions from the bulk solution. The results obtained show a very good agreement between characterization and desalination performance experiments for three commercial electrodes with different structure topology.

  2. Simultaneous measurements of wire electrode surface contamination and corona discharge characteristics in an air-cleaning electrostatic precipitator

    SciTech Connect

    Kanazawa, Seiji; Ohkubo, Toshikazu; Nomoto, Yukiharu; Adachi, Takayoshi; Chang, J.S.

    1997-01-01

    Contamination of the corona wire in a wire-to-plate type air-cleaning electrostatic precipitator is studied experimentally. In order to enhance the contamination of wire, air containing dusts is directly supplied to a part of the wire electrode. Spores of Lycopodium and cigarette smoke particles are used as test dusts. Simultaneous measurements of wire electrode optical images and corona discharge modes are carried out during contamination processes. Results show that corona discharge modes and optical emission from the wire electrode change with time due to the surface contamination. In the case of cigarette smoke, after a time elapsed, streamer coronas appear due to the buildup of smoke particles on the wire surface. After the first streamer generation, the corona current fluctuates with time because the formation and diminution of the projections occur alternately at the different parts on the wire electrode surface.

  3. Ifluence of outer electrode material on ozone production in coaxial negative corona discharge fed by oxygen

    NASA Astrophysics Data System (ADS)

    Orszagh, J.; Skalny, J. D.; Mason, N. J.

    2008-07-01

    The "electric odour", observed by Van Marum when oxygen was passing trough electric spark in 1785, has been later (1839), identified by Ch. F. Schonbeim as a new chemical compound named ozone (Stolarski 1999). Almost from those times ozone is widely used chemical compound. The effect of outer electrode material on the ozone production in negative corona discharge have been studied. Two electrodes with the same dimensions were used in the experiment. One was made of stainless steel other one of brass. First the outer electrode was mechanically cleaned to remove the layer of oxides. The reactor have been filled by pure oxygen and closed. Then the measurement (1 hour measurement of discharge current at the constant voltage and time dependence of ozone concentration in the reactor) was repeated 5 times without cleaning the surface to see the ageing effects. Especially the influence of electrode oxidation on ozone concentration was studied. The experiments have been carried out at atmospheric pressure and ambient temperature. The ozone concentration was measured by UV spectroscopy method directly in the discharge reactor. As one can expect the brass surface was oxidizing faster. After five measurements the electrode surface was covered by layer of greenish oxides. On the other hand the steel electrode surface had no visible oxides layer. The oxidation of the outer electrode had little systematic effect on the ozone concentration but in case of brass electrode the results were scattered in the range from 8000 ppm to 15000 ppm of ozone. It seems that the more oxides are created on the surface the less ozone is produced or the faster the ozone decomposition processes are (see Fig. 1). On the other hand in case of stainless steel electrode the ozone concentrations were comparable in all 5 measurements. Overall ozone concentration was higher in steel electrode. Figure 1: Time dependence of ozone concentration.

  4. 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

  5. Enhanced control of electrochemical response in metallic materials in neural stimulation electrode applications

    SciTech Connect

    Watkins, K.G.; Steen, W.M.; Manna, I.

    1996-12-31

    New means have been investigated for the production of electrode devices (stimulation electrodes) which could be implanted in the human body in order to control pain, activate paralysed limbs or provide electrode arrays for cochlear implants for the deaf or for the relief of tinitus. To achieve this ion implantation and laser materials processing techniques were employed. Ir was ion implanted in Ti-6Al-4V alloy and the surface subsequently enriched in the noble metal by dissolution in sulphuric acid. For laser materials processing techniques, investigation has been carried out on the laser cladding and laser alloying of Ir in Ti wire. A particular aim has been the determination of conditions required for the formation of a two phase Ir, Ir-rich, and Ti-rich microstructure which would enable subsequent removal of the non-noble phase to leave a highly porous noble metal with large real surface area and hence improved charge carrying capacity compared with conventional non porous electrodes. Evaluation of the materials produced has been carried out using repetitive cyclic voltammetry, amongst other techniques. For laser alloyed Ir on Ti wire, it has been found that differences in the melting point and density of the materials makes control of the cladding or alloying process difficult. Investigation of laser process parameters for the control of alloying and cladding in this system was carried out and a set of conditions for the successful production of two phase Ir-rich and Ti-rich components in a coating layer with strong metallurgical bonding to the Ti alloy substrate was derived. The laser processed material displays excellent potential for further development in providing stimulation electrodes with the current carrying capacity of Ir but in a form which is malleable and hence capable of formation into smaller electrodes with improved spatial resolution compared with presently employed electrodes.

  6. Zinc/air battery R and D research and development of bifunctional oxygen electrode: Tasks I and II, Final report

    SciTech Connect

    Klein, M.; Viswanathan, S.

    1986-12-01

    Studies were conducted of the bifunctional oxygen electrode. The development of a rechargeable metal-oxygen (air) cell has been hampered to a great extent by the lack of a stable and cost effective oxygen electrode capable of use during both charge and discharge. The first type of bifunctional electrode consists of two distinct catalytifc layers. The oxygen reduction catalyst layer containing a supported gold catalyst is in contact with a hydrophilic nickel layer in which evolution of oxygen takes place. Loadings of gold from 0.5 to 1.0 mg/cm/sup 2/ were investigated; carbon, graphite, metal, and spinel oxides were evaluated as substrates. The second part of the research effort was centered on developing a reversible oxygen electrode containing only one catalytic layer for both reduction and evolution of oxygen. The work was directed specifically to the study of perovskite type of oxides with the composition AA/sup 1/BO/sub 3/ where A is an element of the lanthanide series, A/sup 1/ is an alkaline earth metal and B, a first row transition element. Initial polarization data obtained in unscrubbed air gave a value of approximately 200 millivolts vs Hg/HgO reference electrode at a current density of 50 ma/cm/sup 2/. Electrodes were made both by roll-bonding and by pelletizing techniques and tested for polarization and cycle life. This study also indicates the optimum process conditions for the manufacture of oxides and fabrication of electrodes.

  7. Investigation on the Charging Process of Li2O2-Based Air Electrodes in Li-O2 Batteries with Organic Carbonate Electrolytes

    SciTech Connect

    Xu, Wu; Viswanathan, Vilayanur V.; Wang, Deyu; Towne, Silas A.; Xiao, Jie; Nie, Zimin; Hu, Dehong; Zhang, Jiguang

    2011-04-15

    The charge processes of Li-O2 batteries were investigated by analyzing the gas evolution by in situ gas chromatography-mass spectroscopy (GC/MS) technique. The mixture of Li2O2/Fe3O4/Super P carbon/polyvinylidene fluoride (PVDF) was used as the starting air electrode material and 1M LiTFSI in carbonate-based solvents was used as electrolyte. It was found that Li2O2 is reactive to 1-methyl-2-pyrrolidinone and PVDF binder used in the electrode preparation. During the 1st charge (up to 4.6 V), O2 was the main component in the gases released. The amount of O2 measured by GC/MS was consistent with the amount of Li2O2 decomposed in the electrochemical process as measured by the charge capacity, indicative of the good chargeability of Li2O2. However, after the cell was discharged to 2.0 V in O2 atmosphere and re-charged to ~ 4.6 V in the second cycle, CO2 was dominant in the released gases. Further analysis of the discharged air electrode by X-ray diffraction and Fourier transform infrared spectroscopy indicated that lithium-containing carbonate species (lithium alkyl carbonate and/or Li2CO3) were the main reaction products. Therefore, compatible electrolyte and electrodes as well as the electrode preparation procedures need to be developed for long term operation of rechargeable Li-O2 or Li-air batteries.

  8. Nanostructured pseudocapacitive materials decorated 3D graphene foam electrodes for next generation supercapacitors.

    PubMed

    Patil, Umakant; Lee, Su Chan; Kulkarni, Sachin; Sohn, Ji Soo; Nam, Min Sik; Han, Suhyun; Jun, Seong Chan

    2015-04-28

    Nowadays, advancement in performance of proficient multifarious electrode materials lies conclusively at the core of research concerning energy storage devices. To accomplish superior capacitance performance the requirements of high capacity, better cyclic stability and good rate capability can be expected from integration of electrochemical double layer capacitor based carbonaceous materials (high power density) and pseudocapacitive based metal hydroxides/oxides or conducting polymers (high energy density). The envisioned three dimensional (3D) graphene foams are predominantly advantageous to extend potential applicability by offering a large active surface area and a highly conductive continuous porous network for fast charge transfer with decoration of nanosized pseudocapacitive materials. In this article, we review the latest methodologies and performance evaluation for several 3D graphene based metal oxides/hydroxides and conducting polymer electrodes with improved electrochemical properties for next-generation supercapacitors. The most recent research advancements of our and other groups in the field of 3D graphene based electrode materials for supercapacitors are discussed. To assess the studied materials fully, a careful interpretation and rigorous scrutiny of their electrochemical characteristics is essential. Auspiciously, both nano-structuration as well as confinement of metal hydroxides/oxides and conducting polymers onto a conducting porous 3D graphene matrix play a great role in improving the performance of electrodes mainly due to: (i) active material access over large surface area with fast charge transportation; (ii) synergetic effect of electric double layer and pseudocapacitive based charge storing.

  9. Nanostructured pseudocapacitive materials decorated 3D graphene foam electrodes for next generation supercapacitors

    NASA Astrophysics Data System (ADS)

    Patil, Umakant; Lee, Su Chan; Kulkarni, Sachin; Sohn, Ji Soo; Nam, Min Sik; Han, Suhyun; Jun, Seong Chan

    2015-04-01

    Nowadays, advancement in performance of proficient multifarious electrode materials lies conclusively at the core of research concerning energy storage devices. To accomplish superior capacitance performance the requirements of high capacity, better cyclic stability and good rate capability can be expected from integration of electrochemical double layer capacitor based carbonaceous materials (high power density) and pseudocapacitive based metal hydroxides/oxides or conducting polymers (high energy density). The envisioned three dimensional (3D) graphene foams are predominantly advantageous to extend potential applicability by offering a large active surface area and a highly conductive continuous porous network for fast charge transfer with decoration of nanosized pseudocapacitive materials. In this article, we review the latest methodologies and performance evaluation for several 3D graphene based metal oxides/hydroxides and conducting polymer electrodes with improved electrochemical properties for next-generation supercapacitors. The most recent research advancements of our and other groups in the field of 3D graphene based electrode materials for supercapacitors are discussed. To assess the studied materials fully, a careful interpretation and rigorous scrutiny of their electrochemical characteristics is essential. Auspiciously, both nano-structuration as well as confinement of metal hydroxides/oxides and conducting polymers onto a conducting porous 3D graphene matrix play a great role in improving the performance of electrodes mainly due to: (i) active material access over large surface area with fast charge transportation; (ii) synergetic effect of electric double layer and pseudocapacitive based charge storing.

  10. A review of air pollutant damage to materials

    SciTech Connect

    Yocom, J.E.; Stankunas, A.R.; Bradow, F.V.P.

    1982-06-01

    Report prepared as U.S. contribution to Panel 3 of NATO Committee on Challenges of Modern Society Pilot Study on Air Pollution Control Strategies and Impact Modeling. Panel 3 focuses on air pollutant impact and will publish 4 reports on air pollutants effects; this is the first in the series and covers effects on materials. Reviewed here are physical and economic effects of sulfur oxides, particulate matter, nitrogen oxide, ozone, hydrogen sulfides, fluoride, and ammonia on metals, textiles, paint, building materials, leathers, paper and elastomers. Report is summary of pertinent information in EPA's air quality criteria and EPA-Funded NAS review documents.

  11. Pr4Ni3O10+δ: A new promising oxygen electrode material for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Vibhu, Vaibhav; Rougier, Aline; Nicollet, Clément; Flura, Aurélien; Fourcade, Sébastien; Penin, Nicolas; Grenier, Jean-Claude; Bassat, Jean-Marc

    2016-06-01

    The present work is focused on the study of Pr4Ni3O10+δ as a new cathode material for Solid Oxide Fuel Cells (SOFCs). The structural study leads to an indexation in orthorhombic structure with Fmmm space group, this structure being thermally stable throughout the temperature range up to 1000 °C under air and oxygen. The variation of oxygen content (10+δ) as a function of temperature under different atmospheres show that Pr4Ni3O10+δ is always oxygen over-stoichiometric, which further suggests its MIEC properties. The polarization resistance (Rp) of Pr4Ni3O10+δ electrode is measured for GDC/co-sintered and two-step sintered half cells. The Rp for co-sintered sample is found to be 0.16 Ω cm2 at 600 °C under air, which is as low as the one of highest performing Pr2NiO4+δ nickelate (Rp = 0.15 Ω cm2 at 600 °C). Moreover, an anode supported (Ni-YSZ//YSZ) single cell including GDC//Pr4Ni3O10+δ co-sintered electrode shows a maximum power density of 1.60 W cm-2 at 800 °C and 0.68 W cm-2 at 700 °C. Here, the work is emphasized on the very close electrochemical performance of Pr4Ni3O10+δ compared to the one of Pr2NiO4+δ with higher chemical stability, which gives great interests to consider this material as a very interesting oxygen-electrode for SOFCs.

  12. Investigation of materials for inert electrodes in aluminum electrodeposition cells

    SciTech Connect

    Haggerty, J. S.; Sadoway, D. R.

    1987-09-14

    Work was divided into major efforts. The first was the growth and characterization of specimens; the second was Hall cell performance testing. Cathode and anode materials were the subject of investigation. Preparation of specimens included growth of single crystals and synthesis of ultra high purity powders. Special attention was paid to ferrites as they were considered to be the most promising anode materials. Ferrite anode corrosion rates were studied and the electrical conductivities of a set of copper-manganese ferrites were measured. Float Zone, Pendant Drop Cryolite Experiments were undertaken because unsatisfactory choices of candidate materials were being made on the basis of a flawed set of selection criteria applied to an incomplete and sometimes inaccurate data base. This experiment was then constructed to determine whether the apparatus used for float zone crystal growth could be adapted to make a variety of important based melts and their interactions with candidate inert anode materials. The third major topic was Non Consumable Anode (Data Base, Candidate Compositions), driven by our perception that the basis for prior selection of candidate materials was inadequate. Results are presented. 162 refs., 39 figs., 18 tabs.

  13. Generating diffuse discharge via repetitive nanosecond pulses and line-line electrodes in atmospheric air.

    PubMed

    Li, Lee; Liu, Yun-Long; Ge, Ya-Feng; Bin, Yu; Huang, Jia-Jia; Lin, Fo-Chan

    2013-10-01

    Diffuse discharge in atmospheric air can generate extremely high power density and large-scale non-thermal plasma. An achievable method of generating diffuse discharge is reported in this paper. Based on the resonance theory, a compact high-voltage repetitive nanosecond pulse generator (HRNPG) has been developed as discharge excitation source. The HRNPG mainly consists of repetitive charging circuit, Tesla transformer and sharpening switch. With the voltage lower than 1.0 kV, the primary repetitive charging circuit comprises two fast thyristors as low-voltage switches. A spiral Tesla transformer is designed to provide a peak transformation ratio of more than 100. The HRNPG prototype is capable of generating a pulse with over 100 kV peak voltage and ~30 ns rise-time at the repetition frequency of 500 Hz. Using the copper line electrodes with a diameter of 0.4 mm, the gaps with highly non-uniform electric field are structured. With the suitable gap spacing and applied pulse, the glow-like diffuse discharge has been generated in line-type and ring-type electrode pairs. Some typical images are presented. PMID:24182161

  14. Generating diffuse discharge via repetitive nanosecond pulses and line-line electrodes in atmospheric air.

    PubMed

    Li, Lee; Liu, Yun-Long; Ge, Ya-Feng; Bin, Yu; Huang, Jia-Jia; Lin, Fo-Chan

    2013-10-01

    Diffuse discharge in atmospheric air can generate extremely high power density and large-scale non-thermal plasma. An achievable method of generating diffuse discharge is reported in this paper. Based on the resonance theory, a compact high-voltage repetitive nanosecond pulse generator (HRNPG) has been developed as discharge excitation source. The HRNPG mainly consists of repetitive charging circuit, Tesla transformer and sharpening switch. With the voltage lower than 1.0 kV, the primary repetitive charging circuit comprises two fast thyristors as low-voltage switches. A spiral Tesla transformer is designed to provide a peak transformation ratio of more than 100. The HRNPG prototype is capable of generating a pulse with over 100 kV peak voltage and ~30 ns rise-time at the repetition frequency of 500 Hz. Using the copper line electrodes with a diameter of 0.4 mm, the gaps with highly non-uniform electric field are structured. With the suitable gap spacing and applied pulse, the glow-like diffuse discharge has been generated in line-type and ring-type electrode pairs. Some typical images are presented.

  15. Generating diffuse discharge via repetitive nanosecond pulses and line-line electrodes in atmospheric air

    NASA Astrophysics Data System (ADS)

    Li, Lee; Liu, Yun-Long; Ge, Ya-Feng; Bin, Yu; Huang, Jia-Jia; Lin, Fo-Chan

    2013-10-01

    Diffuse discharge in atmospheric air can generate extremely high power density and large-scale non-thermal plasma. An achievable method of generating diffuse discharge is reported in this paper. Based on the resonance theory, a compact high-voltage repetitive nanosecond pulse generator (HRNPG) has been developed as discharge excitation source. The HRNPG mainly consists of repetitive charging circuit, Tesla transformer and sharpening switch. With the voltage lower than 1.0 kV, the primary repetitive charging circuit comprises two fast thyristors as low-voltage switches. A spiral Tesla transformer is designed to provide a peak transformation ratio of more than 100. The HRNPG prototype is capable of generating a pulse with over 100 kV peak voltage and ˜30 ns rise-time at the repetition frequency of 500 Hz. Using the copper line electrodes with a diameter of 0.4 mm, the gaps with highly non-uniform electric field are structured. With the suitable gap spacing and applied pulse, the glow-like diffuse discharge has been generated in line-type and ring-type electrode pairs. Some typical images are presented.

  16. [Electrode configuration as a factor affecting electricity generation in air-cathode microbial fuel cell].

    PubMed

    You, Shi-Jie; Zhao, Qing-Liang; Jiang, Jun-Qiu

    2006-11-01

    In air-cathode microbial fuel cell (ACMFC), oxygen diffused into the reactor from cathode without PEM can be reduced as electron acceptor via aerobic respiration by facultative microorganisms, resulting in either a decreasing of power generation or electron loss. In this study, ACMFC1 and ACMFC2 with different electrode configuration were compared to examine power density and electron recovery from glucose. The results showed that ACMFC1 generated a maximum power density of 3 070mW/m3 with internal resistance of 302.141 and anode potential of -323mV; while maximum power density of 9 800mW/m3 for ACMFC2 was obtained with internal resistance of 107.79omega and anode potential of -442mV. ACMFC2 could sustain generating electricity for nearly 220 h (ERE of 30.1%), comparing with ACMFC1 of less than 50 h (ERE of 9.78%) under batch operation. Therefore, an improved design for electrode configuration of ACMFC can be performed to generate higher power with low internal resistance, meanwhile, achieve increasing electron recovery simultaneously.

  17. Development of Nano-structured Electrode Materials for High Performance Energy Storage System

    NASA Astrophysics Data System (ADS)

    Huang, Zhendong

    Systematic studies have been done to develop a low cost, environmental-friendly facile fabrication process for the preparation of high performance nanostructured electrode materials and to fully understand the influence factors on the electrochemical performance in the application of lithium ion batteries (LIBs) or supercapacitors. For LIBs, LiNi1/3Co1/3Mn1/3O2 (NCM) with a 1D porous structure has been developed as cathode material. The tube-like 1D structure consists of inter-linked, multi-facet nanoparticles of approximately 100-500nm in diameter. The microscopically porous structure originates from the honeycomb-shaped precursor foaming gel, which serves as self-template during the stepwise calcination process. The 1D NCM presents specific capacities of 153, 140, 130 and 118mAh·g-1 at current densities of 0.1C, 0.5C, 1C and 2C, respectively. Subsequently, a novel stepwise crystallization process consisting of a higher crystallization temperature and longer period for grain growth is employed to prepare single crystal NCM nanoparticles. The modified sol-gel process followed by optimized crystallization process results in significant improvements in chemical and physical characteristics of the NCM particles. They include a fully-developed single crystal NCM with uniform composition and a porous NCM architecture with a reduced degree of fusion and a large specific surface area. The NCM cathode material with these structural modifications in turn presents significantly enhanced specific capacities of 173.9, 166.9, 158.3 and 142.3mAh·g -1 at 0.1C, 0.5C, 1C and 2C, respectively. Carbon nanotube (CNT) is used to improve the relative low power capability and poor cyclic stability of NCM caused by its poor electrical conductivity. The NCM/CNT nanocomposites cathodes are prepared through simply mixing of the two component materials followed by a thermal treatment. The CNTs were functionalized to obtain uniformly-dispersed MWCNTs in the NCM matrix. The electrochemical

  18. Magnetically Diffused Radial Electric-Arc Air Heater Employing Water-Cooled Copper Electrodes

    NASA Technical Reports Server (NTRS)

    Mayo, R. F.; Davis, D. D., Jr.

    1962-01-01

    A magnetically rotated electric-arc air heater has been developed that is novel in that an intense magnetic field of the order of 10,000 to 25,000 gauss is employed. This field is supplied by a coil that is connected in series with the arc. Experimentation with this heater has shown that the presence of an intense magnetic field transverse to the arc results in diffusion of the arc and that the arc has a positive effective resistance. With the field coil in series with the arc, highly stable arc operation is obtained from a battery power supply. External ballast is not required to stabilize the arc when it is operating at maximum power level. The electrode erosion rate is so low that the airstream contamination is no more than 0.07 percent and may be substantially less.

  19. Bifunctional Manganese Ferrite/Polyaniline Hybrid as Electrode Material for Enhanced Energy Recovery in Microbial Fuel Cell.

    PubMed

    Khilari, Santimoy; Pandit, Soumya; Varanasi, Jhansi L; Das, Debabrata; Pradhan, Debabrata

    2015-09-23

    Microbial fuel cells (MFCs) are emerging as a sustainable technology for waste to energy conversion where electrode materials play a vital role on its performance. Platinum (Pt) is the most common material used as cathode catalyst in the MFCs. However, the high cost and low earth abundance associated with Pt prompt the researcher to explore inexpensive catalysts. The present study demonstrates a noble metal-free MFC using a manganese ferrite (MnFe2O4)/polyaniline (PANI)-based electrode material. The MnFe2O4 nanoparticles (NPs) and MnFe2O4 NPs/PANI hybrid composite not only exhibited superior oxygen reduction reaction (ORR) activity for the air cathode but also enhanced anode half-cell potential upon modifying carbon cloth anode in the single-chambered MFC. This is attributed to the improved extracellular electron transfer of exoelectrogens due to Fe(3+) in MnFe2O4 and its capacitive nature. The present work demonstrates for the first time the dual property of MnFe2O4 NPs/PANI, i.e., as cathode catalyst and an anode modifier, thereby promising cost-effective MFCs for practical applications. PMID:26315619

  20. Layered double hydroxide materials coated carbon electrode: New challenge to future electrochemical power devices

    NASA Astrophysics Data System (ADS)

    Djebbi, Mohamed Amine; Braiek, Mohamed; Namour, Philippe; Ben Haj Amara, Abdesslem; Jaffrezic-Renault, Nicole

    2016-11-01

    Layered double hydroxides (LDHs) have been widely used in the past years due to their unique physicochemical properties and promising applications in electroanalytical chemistry. The present paper is going to focus exclusively on magnesium-aluminum and zinc-aluminum layered double hydroxides (MgAl & ZnAl LDHs) in order to investigate the property and structure of active cation sites located within the layer structure. The MgAl and ZnAl LDH nanosheets were prepared by the constant pH co-precipitation method and uniformly supported on carbon-based electrode materials to fabricate an LDH electrode. Characterization by powder x-ray diffraction, Fourier transform infrared spectroscopy, scanning electron microscopy and transmission electron microscopy revealed the LDH form and well-crystallized materials. Wetting surface properties (hydrophilicity and hydrophobicity) of both prepared LDHs were recorded by contact angle measurement show hydrophilic character and basic property. The electrochemical performance of these hybrid materials was investigated by mainly cyclic voltammetry, electrochemical impedance spectroscopy and chronoamperometry techniques to identify the oxidation/reduction processes at the electrode/electrolyte interface and the effect of the divalent metal cations in total reactivity. The hierarchy of the modified electrode proves that the electronic conductivity of the bulk material is considerably dependent on the divalent cation and affects the limiting parameter of the overall redox process. However, MgAl LDH shows better performance than ZnAl LDH, due to the presence of magnesium cations in the layers. Following the structural, morphological and electrochemical behavior studies of both synthesized LDHs, the prepared LDH modified electrodes were tested through microbial fuel cell configuration, revealing a remarkable, potential new pathway for high-performance and cost-effective electrode use in electrochemical power devices.

  1. 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.

  2. Graphene-carbon nanotube hybrid materials and use as electrodes

    DOEpatents

    Tour, James M.; Zhu, Yu; Li, Lei; Yan, Zheng; Lin, Jian

    2016-09-27

    Provided are methods of making graphene-carbon nanotube hybrid materials. Such methods generally include: (1) associating a graphene film with a substrate; (2) applying a catalyst and a carbon source to the graphene film; and (3) growing carbon nanotubes on the graphene film. The grown carbon nanotubes become covalently linked to the graphene film through carbon-carbon bonds that are located at one or more junctions between the carbon nanotubes and the graphene film. In addition, the grown carbon nanotubes are in ohmic contact with the graphene film through the carbon-carbon bonds at the one or more junctions. The one or more junctions may include seven-membered carbon rings. Also provided are the formed graphene-carbon nanotube hybrid materials.

  3. A Metal-Free, Free-Standing, Macroporous Graphene@g-C₃N₄ Composite Air Electrode for High-Energy Lithium Oxygen Batteries.

    PubMed

    Luo, Wen-Bin; Chou, Shu-Lei; Wang, Jia-Zhao; Zhai, Yu-Chun; Liu, Hua-Kun

    2015-06-01

    The nonaqueous lithium oxygen battery is a promising candidate as a next-generation energy storage system because of its potentially high energy density (up to 2-3 kW kg(-1)), exceeding that of any other existing energy storage system for storing sustainable and clean energy to reduce greenhouse gas emissions and the consumption of nonrenewable fossil fuels. To achieve high energy density, long cycling stability, and low cost, the air electrode structure and the electrocatalysts play important roles. Here, a metal-free, free-standing macroporous graphene@graphitic carbon nitride (g-C3N4) composite air cathode is first reported, in which the g-C3N4 nanosheets can act as efficient electrocatalysts, and the macroporous graphene nanosheets can provide space for Li2O2 to deposit and also promote the electron transfer. The electrochemical results on the graphene@g-C3N4 composite air electrode show a 0.48 V lower charging plateau and a 0.13 V higher discharging plateau than those of pure graphene air electrode, with a discharge capacity of nearly 17300 mA h g(-1)(composite) . Excellent cycling performance, with terminal voltage higher than 2.4 V after 105 cycles at 1000 mA h g(-1)(composite) capacity, can also be achieved. Therefore, this hybrid material is a promising candidate for use as a high energy, long-cycle-life, and low-cost cathode material for lithium oxygen batteries. PMID:25688745

  4. Synthesis and evaluation of polythiocyanogen (SCN) x as a rechargeable lithium-ion battery electrode material

    NASA Astrophysics Data System (ADS)

    Krishnan, Palanichamy; Advani, Suresh G.; Prasad, Ajay K.

    Polythiocyanogen, (SCN) x, is a promising lithium-ion battery electrode material due to its high theoretical capacity (462 mAh g -1), safe operation, inexpensive raw materials, and a simple and less energy-intensive manufacturing process. The (SCN) x was prepared from the solution of trithiocyanate (SCN) 3 - in methylene dichloride (MDC), which was prepared by electrochemical oxidation of ammonium thiocyanate (NH 4SCN) in a two-phase electrolysis medium of 1.0 M NH 4SCN in 0.50 M H 2SO 4 + MDC. The (SCN) 3 - underwent auto catalytic polymerization to (SCN) x during MDC removal. Battery electrodes with (SCN) x as the active material were prepared, and tested in Swagelok cells using lithium foil as the counter and reference electrode. The cells delivered capacities in the range of 200-275 mAh g -1 at the discharge-charge rate of 0.2 C. The cells were tested up to 20 cycles and showed repeatable performance with a coulombic efficiency of 97% at the 20th cycle. The results presented here indicate that (SCN) x is a promising lithium-ion battery electrode-material candidate for further studies.

  5. 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.

  6. APEX (Air Pollution Exercise) Volume 20: Reference Materials.

    ERIC Educational Resources Information Center

    Environmental Protection Agency, Research Triangle Park, NC. Office of Manpower Development.

    The Reference Materials Manual is part of a set of 21 manuals (AA 001 009-001 029) used in APEX (Air Pollution Exercise), a computerized college and professional level "real world" game simulation of a community with urban and rural problems, industrial activities, and air pollution difficulties. For the purposes of the gaming exercise, APEX…

  7. 33 CFR 183.112 - Flotation material and air chambers.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... SECURITY (CONTINUED) BOATING SAFETY BOATS AND ASSOCIATED EQUIPMENT Flotation Requirements for Inboard Boats, Inboard/Outdrive Boats, and Airboats § 183.112 Flotation material and air chambers. (a)...

  8. 33 CFR 183.112 - Flotation material and air chambers.

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... SECURITY (CONTINUED) BOATING SAFETY BOATS AND ASSOCIATED EQUIPMENT Flotation Requirements for Inboard Boats, Inboard/Outdrive Boats, and Airboats § 183.112 Flotation material and air chambers. (a)...

  9. 33 CFR 183.112 - Flotation material and air chambers.

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... SECURITY (CONTINUED) BOATING SAFETY BOATS AND ASSOCIATED EQUIPMENT Flotation Requirements for Inboard Boats, Inboard/Outdrive Boats, and Airboats § 183.112 Flotation material and air chambers. (a)...

  10. 33 CFR 183.112 - Flotation material and air chambers.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... SECURITY (CONTINUED) BOATING SAFETY BOATS AND ASSOCIATED EQUIPMENT Flotation Requirements for Inboard Boats, Inboard/Outdrive Boats, and Airboats § 183.112 Flotation material and air chambers. (a)...

  11. Metal-air cell with ion exchange material

    SciTech Connect

    Friesen, Cody A.; Wolfe, Derek; Johnson, Paul Bryan

    2015-08-25

    Embodiments of the invention are related to anion exchange membranes used in electrochemical metal-air cells in which the membranes function as the electrolyte material, or are used in conjunction with electrolytes such as ionic liquid electrolytes.

  12. Recent Advances in Polymeric Materials Used as Electron Mediators and Immobilizing Matrices in Developing Enzyme Electrodes

    PubMed Central

    Moyo, Mambo; Okonkwo, Jonathan O.; Agyei, Nana M.

    2012-01-01

    Different classes of polymeric materials such as nanomaterials, sol-gel materials, conducting polymers, functional polymers and biomaterials have been used in the design of sensors and biosensors. Various methods have been used, for example from direct adsorption, covalent bonding, crossing-linking with glutaraldehyde on composites to mixing the enzymes or use of functionalized beads for the design of sensors and biosensors using these polymeric materials in recent years. It is widely acknowledged that analytical sensing at electrodes modified with polymeric materials results in low detection limits, high sensitivities, lower applied potential, good stability, efficient electron transfer and easier immobilization of enzymes on electrodes such that sensing and biosensing of environmental pollutants is made easier. However, there are a number of challenges to be addressed in order to fulfill the applications of polymeric based polymers such as cost and shortening the long laboratory synthetic pathways involved in sensor preparation. Furthermore, the toxicological effects on flora and fauna of some of these polymeric materials have not been well studied. Given these disadvantages, efforts are now geared towards introducing low cost biomaterials that can serve as alternatives for the development of novel electrochemical sensors and biosensors. This review highlights recent contributions in the development of the electrochemical sensors and biosensors based on different polymeric material. The synergistic action of some of these polymeric materials and nanocomposites imposed when combined on electrode during sensing is discussed. PMID:22368503

  13. Rock-salt-type lithium metal sulphides as novel positive-electrode materials

    PubMed Central

    Sakuda, Atsushi; Takeuchi, Tomonari; Okamura, Kazuhiro; Kobayashi, Hironori; Sakaebe, Hikari; Tatsumi, Kuniaki; Ogumi, Zempachi

    2014-01-01

    One way of increasing the energy density of lithium-ion batteries is to use electrode materials that exhibit high capacities owing to multielectron processes. Here, we report two novel materials, Li2TiS3 and Li3NbS4, which were mechanochemically synthesised at room temperature. When used as positive-electrode materials, Li2TiS3 and Li3NbS4 charged and discharged with high capacities of 425 mA h g−1 and 386 mA h g−1, respectively. These capacities correspond to those resulting from 2.5- and 3.5-electron processes. The average discharge voltage was approximately 2.2 V. It should be possible to prepare a number of high-capacity materials on the basis of the concept used to prepare Li2TiS3 and Li3NbS4. PMID:24811191

  14. 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.

  15. An ion-selective electrode method for determination of chlorine in geological materials

    USGS Publications Warehouse

    Aruscavage, P. J.; Campbell, E.Y.

    1983-01-01

    A method is presented for the determination of chlorine in geological materials, in which a chloride-selective ion electrode is used after decomposition of the sample with hydrofluoric acid and separation of chlorine in a gas-diffusion cell. Data are presented for 30 geological standard materials. The relative standard deviation of the method is estimated to be better than 8% for amounts of chloride of 10 ??g and greater. ?? 1983.

  16. BiOCl micro-assembles consisting of ultrafine nanoplates: A high performance electro-catalyst for air electrode of Al-air batteries

    NASA Astrophysics Data System (ADS)

    Yuan, Jinlan; Wang, Jin; She, Yiyi; Hu, Jing; Tao, Pengpeng; Lv, Fucong; Lu, Zhouguang; Gu, Yingying

    2014-10-01

    BiOCl micro-assembles appearing spherical and plate-like in shape consisting of ultrafine nanoplates were successfully synthesized by a simple hydrothermal method. The obtained BiOCl micro-assembles were characterized as oxygen reduction reaction (ORR) catalyst for air electrode of aluminum air batteries by using linear polarization and constant-current discharge techniques. The effect of precursor concentration on the electrochemical properties of the air electrodes based on the synthesized BiOCl micro-assembles was intensively investigated. The results demonstrated that the BiOCl catalyst exhibited promising ORR performance. Koutecky-Levich analysis indicated that a two-electron reaction was favored for the ORR mechanism of the BiOCl (0.18) sample.

  17. 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

  18. Nanostructured core-shell electrode materials for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Jiang, Long-bo; Yuan, Xing-zhong; Liang, Jie; Zhang, Jin; Wang, Hou; Zeng, Guang-ming

    2016-11-01

    Core-shell nanostructure represents a unique system for applications in electrochemical energy storage devices. Owing to the unique characteristics featuring high power delivery and long-term cycling stability, electrochemical capacitors (ECs) have emerged as one of the most attractive electrochemical storage systems since they can complement or even replace batteries in the energy storage field, especially when high power delivery or uptake is needed. This review aims to summarize recent progress on core-shell nanostructures for advanced supercapacitor applications in view of their hierarchical architecture which not only create the desired hierarchical porous channels, but also possess higher electrical conductivity and better structural mechanical stability. The core-shell nanostructures include carbon/carbon, carbon/metal oxide, carbon/conducting polymer, metal oxide/metal oxide, metal oxide/conducting polymer, conducting polymer/conducting polymer, and even more complex ternary core-shell nanoparticles. The preparation strategies, electrochemical performances, and structural stabilities of core-shell materials for ECs are summarized. The relationship between core-shell nanostructure and electrochemical performance is discussed in detail. In addition, the challenges and new trends in core-shell nanomaterials development have also been proposed.

  19. PEDOT-based composites as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Zhao, Zhiheng; Richardson, Georgia F.; Meng, Qingshi; Zhu, Shenmin; Kuan, Hsu-Chiang; Ma, Jun

    2016-01-01

    Poly (3, 4-ethylenedioxythiophene) (denoted PEDOT) already has a brief history of being used as an active material in supercapacitors. It has many advantages such as low-cost, flexibility, and good electrical conductivity and pseudocapacitance. However, the major drawback is low stability, which means an obvious capacitance drop after a certain number of charge-discharge cycles. Another disadvantage is its limited capacitance and this becomes an issue for industrial applications. To solve these problems, there are several approaches including the addition of conducting nanofillers to increase conductivity, and mixing or depositing metal oxide to enhance capacitance. Furthermore, expanding the surface area of PEDOT is one of the main methods to improve its performance in energy storage applications through special processes; for example using a three-dimensional substrate or preparing PEDOT aerogel through freeze drying. This paper reviews recent techniques and outcomes of PEDOT based composites for supercapacitors, as well as detailed calculations about capacitances. Finally, this paper outlines the new direction and recent challenges of PEDOT based composites for supercapacitor applications.

  20. Novel Carbon-based Electrode Materials for Up-scaled Microfluidic Fuel Cells

    NASA Astrophysics Data System (ADS)

    Fuerth, Dillon Adam

    In this work, a MFC fabrication procedure including two non-conventional techniques (partial baking and cap-sealing) were employed for the development of an up-scaled microfluidic fuel cell (MFC). Novel carbon-based electrode materials were employed, including carbon foam, fibre, and cloth, the results from which were compared with traditionally-employed carbon paper. The utilization of carbon cloth led to 15% of the maximum power that resulted from carbon paper; however, carbon fibre led to a 24.6% higher power density than carbon paper (normalized by electrode volume). When normalized by projected electrode area, the utilization of carbon foams resulted in power densities up to 42.5% higher than that from carbon paper. The impact of catalyst loading on MFC performance was also investigated, with an increase from 10.9 to 48.3 mgPt cm-2 resulting in a 195% increase in power density.

  1. Method of preparing an electrode material of lithium-aluminum alloy

    DOEpatents

    Settle, Jack L.; Myles, Kevin M.; Battles, James E.

    1976-01-01

    A solid compact having a uniform alloy composition of lithium and aluminum is prepared as a negative electrode for an electrochemical cell. Lithium losses during preparation are minimized by dissolving aluminum within a lithium-rich melt at temperatures near the liquidus temperatures. The desired alloy composition is then solidified and fragmented. The fragments are homogenized to a uniform composition by annealing at a temperature near the solidus temperature. After comminuting to fine particles, the alloy material can be blended with powdered electrolyte and pressed into a solid compact having the desired electrode shape. In the preparation of some electrodes, an electrically conductive metal mesh is embedded into the compact as a current collector.

  2. Synthesis of nitrogen-doped porous carbon nanofibers as an efficient electrode material for supercapacitors.

    PubMed

    Chen, Li-Feng; Zhang, Xu-Dong; Liang, Hai-Wei; Kong, Mingguang; Guan, Qing-Fang; Chen, Ping; Wu, Zhen-Yu; Yu, Shu-Hong

    2012-08-28

    Supercapacitors (also known as ultracapacitors) are considered to be the most promising approach to meet the pressing requirements of energy storage. Supercapacitive electrode materials, which are closely related to the high-efficiency storage of energy, have provoked more interest. Herein, we present a high-capacity supercapacitor material based on the nitrogen-doped porous carbon nanofibers synthesized by carbonization of macroscopic-scale carbonaceous nanofibers (CNFs) coated with polypyrrole (CNFs@polypyrrole) at an appropriate temperature. The composite nanofibers exhibit a reversible specific capacitance of 202.0 F g(-1) at the current density of 1.0 A g(-1) in 6.0 mol L(-1) aqueous KOH electrolyte, meanwhile maintaining a high-class capacitance retention capability and a maximum power density of 89.57 kW kg(-1). This kind of nitrogen-doped carbon nanofiber represents an alternative promising candidate for an efficient electrode material for supercapacitors.

  3. Materials and fabrication of electrode scaffolds for deposition of MnO2 and their true performance in supercapacitors

    NASA Astrophysics Data System (ADS)

    Cao, Jianyun; Li, Xiaohong; Wang, Yaming; Walsh, Frank C.; Ouyang, Jia-Hu; Jia, Dechang; Zhou, Yu

    2015-10-01

    MnO2 is a promising electrode material for high energy supercapacitors because of its large pseudo-capacitance. However, MnO2 suffers from low electronic conductivity and poor cation diffusivity, which results in poor utilization and limited rate performance of traditional MnO2 powder electrodes, obtained by pressing a mixed paste of MnO2 powder, conductive additive and polymer binder onto metallic current collectors. Developing binder-free MnO2 electrodes by loading nanoscale MnO2 deposits on pre-fabricated device-ready electrode scaffolds is an effective way to achieve both high power and energy performance. These electrode scaffolds, with interconnected skeletons and pore structures, will not only provide mechanical support and electron collection as traditional current collectors but also fast ion transfer tunnels, leading to high MnO2 utilization and rate performance. This review covers design strategies, materials and fabrication methods for the electrode scaffolds. Rational evaluation of the true performance of these electrodes is carried out, which clarifies that some of the electrodes with as-claimed exceptional performances lack potential in practical applications due to poor mass loading of MnO2 and large dead volume of inert scaffold materials/void spaces in the electrode structure. Possible ways to meet this challenge and bring MnO2 electrodes from laboratory studies to real-world applications are considered.

  4. Loading and utilization of active material in nickel composite electrodes: optimization

    SciTech Connect

    Lee, W.W.; Ferrando, W.A.; Sutula, R.A.

    1984-12-01

    As an attempt to reduce nickel battery weight, the nickel composite electrode, has been under development. Investigations were undertaken to determine the optimum conditions for loading and utilizing nickel hydroxide active material in nickel composite electrodes. The main emphasis was placed on the improvement of both loading efficiency by electrochemical impregnation and utilization efficiency of the Ni(OH)2 active material. The efficiencies were examined as functions of such electrochemical conditions as current density, nickel concentration, pH, temperature of the impregnating bath, the continuity of current flow and manner of adding Co(OH)S additive. Also studied was the loading efficiency of chemical impregnation (polarization method) and the suspension method which enables a direct loading of externally prepared active material into the composite body. The most important factor for a quick utilization of the active material was found to be the additive distribution. A model of the additive distribution in the active material is proposed to account for different patterns of utilization exhibited by the electrodes.

  5. 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

  6. Evaluation of materials proposed for the construction of the plasma electrode Pockels cell (PEPC) on beamlet

    SciTech Connect

    Roberts, D.; Robb, C.; DeYoreo, J.; Atherton, J.

    1992-11-01

    The proposed upgrade of the NOVA laser system at Lawrence Livermore National Laboratory employs a multipass architecture that requires an optical switch to emit the laser light at the appropriate fluence. This Pockels cell-based optical switch does not use traditional ring or thin-film electrodes because of the large aperture and high fluence of the laser system. Rather, it uses a plasma electrode Pockels cell with a KD*P crystal as the electro-optical medium. A discharge plasma is formed on each side of the electro-optic crystal and high voltage is applied across the crystal through the plasma electrode to initiate optical switching. In October 1991 we began evaluating materials suggested for the large aperture plasma electrode optical switch. Previous experiments suggested that switching performance could be significantly affected by the deterioration of cell materials. The final prototype switch tested used polyethylene for the switch body, Mykroy for the mid-plane and a silicone vulcanite to encapsulate the KD*P crystal. The encapsulant easily compensated for the effect of assembling the optical switch and we measured no strain-induced birefringence in the crystal after encapsulation. Oxygen was eventually added to the plasma to react with the sputtered carbon from the cathode and produce a gaseous effluent. As an added benefit, the production of ozone absorbed most of the ultra violet radiation affecting the encapsulant. All the materials tested decomposed and produced volatiles, although we have seen no change in the damage threshold of exposed optical surfaces tested to date. The following is an evaluation of the recommended materials for major cell components using published manufacturers data, experimental results from our Material Evaluation Apparatus, and outgassing performance and sputtering data produced at the Laboratory`s Vacuum Process Lab.

  7. Nickel-Tin Electrode Materials for Nonaqueous Li-Ion Cells

    NASA Technical Reports Server (NTRS)

    Ehrlich, Grant M.; Durand, Christopher

    2005-01-01

    Experimental materials made from mixtures of nickel and tin powders have shown promise for use as the negative electrodes of rechargeable lithium-ion electrochemical power cells. During charging (or discharging) of a lithium-ion cell, lithium ions are absorbed into (or desorbed from, respectively) the negative electrode, typically through an intercalation or alloying process. The negative electrodes (for this purpose, designated as anodes) in state-of-the-art Li-ion cells are made of graphite, in which intercalation occurs. Alternatively, the anodes can be made from metals, in which alloying can occur. For reasons having to do with the electrochemical potential of intercalated lithium, metallic anode materials (especially materials containing tin) are regarded as safer than graphite ones; in addition, such metallic anode materials have been investigated in the hope of obtaining reversible charge/discharge capacities greater than those of graphite anodes. However, until now, each of the tin-containing metallic anode formulations tested has been found to be inadequate in some respect.

  8. Film of lignocellulosic carbon material for self-supporting electrodes in electric double-layer capacitors

    NASA Astrophysics Data System (ADS)

    Funabashi, Tsubasa; Mizuno, Jun; Sato, Masamichi; Kitajima, Masao; Matsuura, Makoto; Shoji, Shuichi

    2013-09-01

    A novel thin, wood-based carbon material with heterogeneous pores, film of lignocellulosic carbon material (FLCM), was successfully fabricated by carbonizing softwood samples of Picea jezoensis (Jezo spruce). Simultaneous increase in the specific surface area of FLCM and its affinity for electrolyte solvents in an electric double-layer capacitor (EDLC) were achieved by the vacuum ultraviolet/ozone (VUV/O3) treatment. This treatment increased the specific surface area of FLCM by 50% over that of original FLCM. The results obtained in this study confirmed that FLCM is an appropriate self-supporting EDLC electrode material without any warps and cracks.

  9. Recent development of carbon electrode materials and their bioanalytical and environmental applications.

    PubMed

    Zhang, Wei; Zhu, Shuyun; Luque, Rafael; Han, Shuang; Hu, Lianzhe; Xu, Guobao

    2016-02-01

    Carbon materials have been extensively investigated due to their diversity, favorable properties, and active applications including electroanalytical chemistry. This critical review discusses new synthetic methods, novel carbon materials, new properties and electroanalytical applications of carbon materials particularly related to the preparation as well as bioanalytical and environmental applications of highly oriented pyrolytic graphite, graphene, carbon nanotubes, various carbon films (e.g. pyrolyzed carbon films, boron-doped diamond films and diamond-like carbon films) and screen printing carbon electrodes. Future perspectives in the field have also been discussed (366 references).

  10. Equivalent ambipolar carrier injection of electrons and holes with Au electrodes in air-stable field effect transistors

    SciTech Connect

    Kanagasekaran, Thangavel E-mail: Shimotani@m.tohoku.ac.jp Ikeda, Susumu; Kumashiro, Ryotaro; Shimotani, Hidekazu E-mail: Shimotani@m.tohoku.ac.jp Shang, Hui; Tanigaki, Katsumi E-mail: Shimotani@m.tohoku.ac.jp

    2015-07-27

    Carrier injection from Au electrodes to organic thin-film active layers can be greatly improved for both electrons and holes by nano-structural surface control of organic semiconducting thin films using long-chain aliphatic molecules on a SiO{sub 2} gate insulator. In this paper, we demonstrate a stark contrast for a 2,5-bis(4-biphenylyl)bithiophene (BP2T) active semiconducting layer grown on a modified SiO{sub 2} dielectric gate insulator between two different modifications of tetratetracontane and poly(methyl methacrylate) thin films. Important evidence that the field effect transistor (FET) characteristics are independent of electrode metals with different work functions is given by the observation of a conversion of the metal-semiconductor contact from the Schottky limit to the Bardeen limit. An air-stable light emitting FET with an Au electrode is demonstrated.

  11. Synthesis and electrochemical characterization of Ni-B/ZIF-8 as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Li, Zhen; Gao, Yilong; Wu, Jianxiang; Zhang, Wei; Tan, Yueyue; Tang, Bohejin

    2016-09-01

    Ni-B/Zeolitic Imidazolate Frameworks-8 (Ni-B/ZIF-8) is synthesized via a series of solvothermal, incipient wetness impregnation and chemical reduction methods. The ZIF-8 serves as the host for the growth of Ni-B forming a Ni-B/ZIF-8 composite. Characterization by X-ray diffraction and Transmission electron microscope reveals the dispersion of Ni-B in ZIF-8. As electrode materials for supercapacitors, ZIF-8, Ni-B and Ni-B/ZIF-8 electrodes exhibit specific capacitances of 147, 563 and 866 F g-1, respectively at a scan rate of 5 mV s-1 and good stability over 500 cycles. In particular, Ni-B/ZIF-8 is a promising material for supercapacitors.

  12. 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.

  13. Electrodes and electrochemical storage cells utilizing tin-modified active materials

    DOEpatents

    Anani, Anaba; Johnson, John; Lim, Hong S.; Reilly, James; Schwarz, Ricardo; Srinivasan, Supramaniam

    1995-01-01

    An electrode has a substrate and a finely divided active material on the substrate. The active material is ANi.sub.x-y-z Co.sub.y Sn.sub.z, wherein A is a mischmetal or La.sub.1-w M.sub.w, M is Ce, Nd, or Zr, w is from about 0.05 to about 1.0, x is from about 4.5 to about 5.5, y is from 0 to about 3.0, and z is from about 0.05 to about 0.5. An electrochemical storage cell utilizes such an electrode as the anode. The storage cell further has a cathode, a separator between the cathode and the anode, and an electrolyte.

  14. Synthesis and electrochemical characterization of Ni-B/ZIF-8 as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Li, Zhen; Gao, Yilong; Wu, Jianxiang; Zhang, Wei; Tan, Yueyue; Tang, Bohejin

    2016-07-01

    Ni-B/Zeolitic Imidazolate Frameworks-8 (Ni-B/ZIF-8) is synthesized via a series of solvothermal, incipient wetness impregnation and chemical reduction methods. The ZIF-8 serves as the host for the growth of Ni-B forming a Ni-B/ZIF-8 composite. Characterization by X-ray diffraction and Transmission electron microscope reveals the dispersion of Ni-B in ZIF-8. As electrode materials for supercapacitors, ZIF-8, Ni-B and Ni-B/ZIF-8 electrodes exhibit specific capacitances of 147, 563 and 866 F g-1, respectively at a scan rate of 5 mV s-1 and good stability over 500 cycles. In particular, Ni-B/ZIF-8 is a promising material for supercapacitors.

  15. 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.

  16. NOVEL ELECTRODE MATERIALS FOR LOW-TEMPERATURE SOLID-OXIDE FUEL CELLS

    SciTech Connect

    X. Lu; C. Xia; Y. Liu; W. Rauch; M. Liu

    2002-12-01

    Composite electrodes consisting of silver and bismuth vanadates exhibit remarkable catalytic activity for oxygen reduction at 500-550 C and greatly reduce the cathode-electrolyte (doped ceria) resistances of low temperature SOFCs, down to about 0.53 {Omega}cm{sup 2} at 500 C and 0.21 {Omega}cm{sup 2} at 550 C. The observed power densities of 231, 332, and 443 mWcm{sup -2} at 500, 525 and 550 C, respectively, make it possible to operate SOFCs at temperatures about 500 C. Using in situ potential dependent FTIR emission spectroscopy, we have found evidence for two, possibly three distinct di-oxygen species present on the electrode surface. We have successfully identified which surface oxygen species is present under a particular electrical or chemical condition and have been able to deduce the reaction mechanisms. This technique will be used to probe the gas-solid interactions at or near the TPB and on the surfaces of mixed-conducting electrodes in an effort to understand the molecular processes relevant to the intrinsic catalytic activity. Broad spectral features are assigned to the polarization-induced changes in the optical properties of the electrode surface layer. The ability of producing vastly different microstructures and morphologies of the very same material is critical to the fabrication of functionally graded electrodes for solid-state electrochemical devices, such as SOFCs and lithium batteries. By carefully adjusting deposition parameters of combustion CVD, we have successfully produced oxide nano-powders with the size of 30 {approx} 200 nm. Porous films with various microstructures and morphologies are also deposited on several substrates by systematic adjustment of deposition parameters. Symmetrical cells were fabricated by depositing cathode materials on both sides of GDC electrolytes.

  17. Review of air-coupled ultrasonic materials characterization.

    PubMed

    Chimenti, D E

    2014-09-01

    This article presents a review of air-coupled ultrasonics employed in the characterization or nondestructive inspection of industrial materials. Developments in air-coupled transduction and electronics are briefly treated, although the emphasis here is on methods of characterization and inspection, and in overcoming limitations inherent in the use of such a tenuous sound coupling medium as air. The role of Lamb waves in plate characterization is covered, including the use of air-coupled acoustic beams to measure the elastic and/or viscoelastic properties of a material. Air-coupled acoustic detection, when other methods are employed to generate high-amplitude sound beams is also reviewed. Applications to civil engineering, acoustic tomography, and the characterization of both paper and wood are dealt with here. A brief summary of developments in air-coupled acoustic arrays and the application of air-coupled methods in nonlinear ultrasonics complete the review. In particular, the work of Professor Bernard Hosten and his collaborators at Bordeaux is carefully examined. PMID:24650685

  18. 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##

  19. The effect of electrode material on the electrogenerated chemiluminescence of luminol

    SciTech Connect

    Vitt, J.E.; Johnson, D.C. ); Engstrom, R.C. )

    1991-06-01

    This paper reports on the oxidation of luminol and its concomitant electrogenerated chemiluminescence (ECL) which were studied at several electrode materials by voltammetry and chronoamperometry. The ECL intensity (I{sub ECL}) was inversely related to the activity of the electrodes. The lowest I{sub ECL}) was measured when luminol was oxidized to 3-aminophthalate (n {approx equal}4 eq mol{sup {minus}1}) at a nearly mass-transport limited rate at glassy carbon. The ECL kinetics were studied and the order of the reaction with respect to luminol was 3/2 at concentrations to ca. 1 mM when O{sub 2} was the coreactant. In the presence of H{sub 2}O{sub 2}, the ECL reaction was first order with respect to luminol. A reaction mechanism is proposed that is consistent with the inetic data and the inverse relationship between electrode activity and I{sub ECL}. The implications of these results are discussed with respect to imaging the spatial distribution of current density at electrode surfaces, including that of PbO{sub 2} films activated by adsorbed Bi(V). A value of 6.6 {times} 10{sup {minus}6} cm{sup 2} s{sup {minus}1} was determined for the diffusion coefficient of luminol in 0.1M NaOH.

  20. Oxygen-doped porous silicon carbide spheres as electrode materials for supercapacitors.

    PubMed

    Kim, Myeongjin; Ju, Hyun; Kim, Jooheon

    2016-01-28

    Oxygen-containing functional groups were introduced onto the surface of the micro- and meso-porous silicon carbide sphere (MMPSiC) in order to investigate the relationship between the electric double layer properties and pseudo-capacitive properties; the degree of oxidation of MMPSiC was also optimized. Although the oxygenated surface functionalities can lead to a decrease in the surface area of MMPSiC, the oxygen functional groups attached to the external surface can participate in the redox reaction, resulting in the enhancement of the total super-capacitive performance. The MMPSiC electrode oxidized for 24 h exhibits a high charge storage capacity with a specific capacitance of 301.1 F g(-1) at a scan rate of 5 mV s(-1), with 86.8% rate performance from 5 to 500 mV s(-1) in 1 M KCl aqueous electrolyte. This outstanding capacitive performance of the MMPSiC electrode oxidized for 24 h can be attributed to the harmonious synergistic effect between the electric double layer capacitive contribution of MMPSiC and the pseudo-capacitive contribution of the oxygen-containing functional groups. These encouraging results demonstrate that the MMPSiC electrode oxidized for 24 h is a promising candidate for high performance electrode materials for supercapacitors. PMID:26752728

  1. Electrical characterization of conductive textile materials and its evaluation as electrodes for venous occlusion plethysmography.

    PubMed

    Goy, C B; Dominguez, J M; Gómez López, M A; Madrid, R E; Herrera, M C

    2013-08-01

    The ambulatory monitoring of biosignals involves the use of sensors, electrodes, actuators, processing tools and wireless communication modules. When a garment includes these elements with the purpose of recording vital signs and responding to specific situations it is call a 'Smart Wearable System'. Over the last years several authors have suggested that conductive textile material (e-textiles) could perform as electrode for these systems. This work aims at implementing an electrical characterization of e-textiles and an evaluation of their ability to act as textile electrodes for lower extremity venous occlusion plethysmography (LEVOP). The e-textile electrical characterization is carried out using two experimental set-ups (in vitro evaluation). Besides, LEVOP records are obtained from healthy volunteers (in vivo evaluation). Standard Ag/AgCl electrodes are used for comparison in all tests. Results shown that the proposed e-textiles are suitable for LEVOP recording and a good agreement between evaluations (in vivo and in vitro) is found. PMID:23875930

  2. 77 FR 17394 - Hazardous Materials: Approval and Communication Requirements for the Safe Transportation of Air...

    Federal Register 2010, 2011, 2012, 2013, 2014

    2012-03-26

    ...: Approval and Communication Requirements for the Safe Transportation of Air Bag Inflators, Air Bag Modules... the Hazardous Materials Regulations applicable to air bag inflators, air bag modules, and seat-belt... material appropriately classified as a ] UN3268 air bag inflator, air bag module, or seat-belt...

  3. Study on electrical characteristics of barrier-free atmospheric air diffuse discharge generated by nanosecond pulses and long wire electrodes

    SciTech Connect

    Li, Lee Liu, Yun-Long; Teng, Yun; Liu, Lun; Pan, Yuan

    2014-07-15

    In room-temperature atmospheric air, the large-scale diffuse plasmas can be generated via high-voltage nanosecond pulses with short rise-time and wire electrodes. Diffuse discharge with the wire electrode length up to 110.0 cm and the discharge spacing of several centimeters has been investigated in this paper. Electrical characteristics of diffuse discharge have been analyzed by their optical photographs and measuring of the voltage and current waveforms. Experimental results show the electrode spacing, and the length of wire electrodes can influence the intensity and mode transition of diffuse discharge. The characteristic of current waveforms is that there are several current oscillation peaks at the time of applied pulsed voltage peak, and at the tail of applied pulse, the conduction current component will compensate the displacement one so that the measured current is unidirectional in diffuse discharge mode. The transition from diffuse discharge to arc discharge is always with the increasing of conduction current density. As for nanosecond pulses with long tail, the long wire electrodes are help for generating non-equilibrium diffuse plasmas.

  4. A high-power low-temperature air plasma generator with a divergent channel of the output electrode

    NASA Astrophysics Data System (ADS)

    Gadzhiev, M. Kh.; Isakaev, E. Kh.; Tyuftyaev, A. S.; Yusupov, D. I.

    2016-01-01

    We have developed and studied a powerful high-enthalpy (H ≥ 20 kJ/g) air plasma jet generator with a divergent channel of the output electrode, which belongs to the class of dc plasmatrons with a thermionic cathode. The plasma generator possesses an efficiency of about 80% and ensures the formation of slightly divergent (2± = 12°) plasma jet with diameter D = 50 mm and a mass-average temperature of 6000-9000 K.

  5. Nitrogen-doped porous graphitic carbon as an excellent electrode material for advanced supercapacitors.

    PubMed

    Sun, Li; Tian, Chungui; Fu, Yu; Yang, Ying; Yin, Jie; Wang, Lei; Fu, Honggang

    2014-01-01

    An advanced supercapacitor material based on nitrogen-doped porous graphitic carbon (NPGC) with high a surface area was synthesized by means of a simple coordination-pyrolysis combination process, in which tetraethyl orthosilicate (TEOS), nickel nitrate, and glucose were adopted as porogent, graphitic catalyst precursor, and carbon source, respectively. In addition, melamine was selected as a nitrogen source owing to its nitrogen-enriched structure and the strong interaction between the amine groups and the glucose unit. A low-temperature treatment resulted in the formation of a NPGC precursor by combination of the catalytic precursor, hydrolyzed TEOS, and the melamine-glucose unit. Following pyrolysis and removal of the catalyst and porogent, the NPGC material showed excellent electrical conductivity owing to its high crystallinity, a large Brunauer-Emmett-Teller surface area (SBET =1027 m(2)  g(-1) ), and a high nitrogen level (7.72 wt %). The unusual microstructure of NPGC materials could provide electrochemical energy storage. The NPGC material, without the need for any conductive additives, showed excellent capacitive behavior (293 F g(-1) at 1 A g(-1) ), long-term cycling stability, and high coulombic efficiency (>99.9 % over 5000 cycles) in KOH when used as an electrode. Notably, in a two-electrode symmetric supercapacitor, NPGC energy densities as high as 8.1 and 47.5 Wh kg(-1) , at a high power density (10.5 kW kg(-1) ), were achieved in 6 M KOH and 1 M Et4 NBF4 -PC electrolytes, respectively. Thus, the synthesized NPGC material could be a highly promising electrode material for advanced supercapacitors and other conversion devices.

  6. 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.

  7. Metal-Air Batteries

    SciTech Connect

    Zhang, Jiguang; Bruce, Peter G.; Zhang, Gregory

    2011-08-01

    Metal-air batteries have much higher specific energies than most currently available primary and rechargeable batteries. Recent advances in electrode materials and electrolytes, as well as new designs on metal-air batteries, have attracted intensive effort in recent years, especially in the development of lithium-air batteries. The general principle in metal-air batteries will be reviewed in this chapter. The materials, preparation methods, and performances of metal-air batteries will be discussed. Two main metal-air batteries, Zn-air and Li-air batteries will be discussed in detail. Other type of metal-air batteries will also be described.

  8. Nickel cobalt oxide nanowire-reduced graphite oxide composite material and its application for high performance supercapacitor electrode material.

    PubMed

    Wang, Xu; Yan, Chaoyi; Sumboja, Afriyanti; Lee, Pooi See

    2014-09-01

    In this paper, we report a facile synthesis method of mesoporous nickel cobalt oxide (NiCo2O4) nanowire-reduced graphite oxide (rGO) composite material by urea induced hydrolysis reaction, followed by sintering at 300 degrees C. P123 was used to stabilize the GO during synthesis, which resulted in a uniform coating of NiCo2O4 nanowire on rGO sheet. The growth mechanism of the composite material is discussed in detail. The NiCo2O4-rGO composite material showed an outstanding electrochemical performance of 873 F g(-1) at 0.5 A g(-1) and 512 F g(-1) at 40 A g(-1). This method provides a promising approach towards low cost and large scale production of supercapacitor electrode material.

  9. 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

  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. Development of materials for open-cycle magnetohydrodynamics (MHD): ceramic electrode. Final report

    SciTech Connect

    Bates, J.L.; Marchant, D.D.

    1986-09-01

    Pacific Northwest Laboratory, supported by the US Department of Energy, developed advanced materials for use in open-cycle, closed cycle magnetohydrodynamics (MHD) power generation, an advanced energy conversion system in which the flow of electrically conducting fluid interacts with an electric field to convert the energy directly into electricity. The purpose of the PNL work was to develop electrodes for the MHD channel. Such electrodes must have: (1) electrical conductivity above 0.01 (ohm-cm)/sup -1/ from near room temperature to 1900/sup 0/K, (2) resistance to both electrochemical and chemical corrosion by both slag and potassium seed, (3) resistance to erosion by high-velocity gases and particles, (4) resistance to thermal shock, (5) adequate thermal conductivity, (6) compatibility with other channel components, particularly the electrical insulators, (7) oxidation-reduction stability, and (8) adequate thermionic emission. This report describes the concept and development of high-temperature, graded ceramic composite electrode materials and their electrical and structural properties. 47 refs., 16 figs., 13 tabs.

  12. In-situ electrochemical route to aerogel electrode materials of graphene and hexagonal CeO₂.

    PubMed

    Chen, Kunfeng; Xue, Dongfeng

    2015-05-15

    We reported a one-step in-situ electrochemical route to synthesize 3D aerogel electrode materials including graphene and hexagonal CeO2 composites. The graphene/CeO2 aerogel can be formed via freeze-drying graphene/CeO2 colloidal solution that was obtained by electrochemical exfoliation of graphite anode and in-situ deposition of CeO2 nanoparticles on graphene sheets in mixing electrolyte of (NH4)2SO4/Ce(NO3)3 and (NH4)2SO4/(NH4)2Ce(NO3)6. The as-obtained CeO2 nanoparticles were closely contacted with graphene, which can enhance the synergistic effect between graphene and CeO2. It is interesting that the as-obtained CeO2 products possessed hexagonal crystal structure that was rarely reported. The Faradaic reactivity of the graphene/CeO2 composites as supercapacitor was enhanced with the increase of the concentration of Ce salts in initial electrolyte. The introduction of CeO2 to graphene electrode can lead to the presence of additional pseudocapacitance besides the electric double-layer capacitance. This simple one-step in-situ electrochemical route can be extended to synthesize various graphene/metal oxide aerogel electrode materials for electric energy storage.

  13. Nanosecond-pulse gliding discharges between point-to-point electrodes in open air

    NASA Astrophysics Data System (ADS)

    Zhang, Cheng; Shao, Tao; Yan, Ping; Zhou, Yuanxiang

    2014-06-01

    In this paper, gliding discharges with a point-to-point electrode geometry were produced by a repetitively pulsed power supply with a rise time of ˜100 ns and a full-width at half-maximum of ˜200 ns. The characteristics of such discharges were investigated by measuring their voltage-current waveforms and taking photographs of their discharge images. Experimental results showed that once the breakdown occurred, the nanosecond-pulse gliding discharges went into a stable stage at all air gaps, behaving in a mode of repetitive sparks. Under certain conditions, a non-stable stage would appear some time after the discharge went into the stable stage, in which the gliding discharges transitioned from repetitive sparks to diffuse discharges. Furthermore, several factors (gap spacing, pulse repetition frequency (PRF) and gas flow rate) influencing the discharge characteristics were investigated. It was observed that both the breakdown voltage and ignition voltage increased with the gap spacing, and a diffuse discharge was absent when the gap spacing was less than 6 mm. The breakdown voltage decreased with the increase in the PRF and its decrease ratio was larger in large gap spacing than in small gap spacing. Discharges would transit from repetitive sparks to diffuse discharges as the flow rate increased. Furthermore, a comparison of nanosecond-pulse and ac gliding discharges was conducted with respect to the power supply. The consumption and energy, the relationship between the power supply and the load, and the time interval between two pulses were three main factors which could lead to different characteristics between the nanosecond-pulse and ac gliding discharges.

  14. MHD air preheaters: Preliminary firing tests for materials selection

    SciTech Connect

    Valente, T. )

    1994-11-01

    The development of power generation by MHD involves many basic and engineering questions. A critical problem is the selection, design and fabrication of construction materials for components, particularly for the air preheaters. Their durability and reliability must be guaranteed for thousands of hours. Open-cycle MHD power plants have indirect air preheating using Cowper-type regenerators. The maximum temperature that can be obtained with the preheating system depends upon the thermo-mechanical properties of the materials used. Commercially available magnesia, alumina and zirconia were fired at 1800, 1850, 1950 and 2000 C with 12-h soak times. The results show that the magnesia-based materials with a high content of pure periclase magnesia are the most promising for air preheater application in a MHD power plant with an indirect preheating system. Four samples behaved well after the 2000 C firing test. Further thermomechanical tests are necessary to select the most suitable materials and to decide the maximum working temperature of the materials. If direct preheating is used, the materials selected might not be the most suitable.

  15. CO2 Activated Carbon Aerogel with Enhanced Electrochemical Performance as a Supercapacitor Electrode Material.

    PubMed

    Lee, Eo Jin; Lee, Yoon Jae; Kim, Jeong Kwon; Hong, Ung Gi; Yi, Jongheop; Yoon, Jung Rag; Song, In Kyu

    2015-11-01

    Carbon aerogel (CA) was prepared by a sol-gel polymerization of resorcinol and formaldehyde in ambient conditions. A series of activated carbon aerogels (ACA-X, X = 1, 2, 3, 4, 5, and 6 h) were then prepared by CO2 activation of CA with a variation of activation time (X) for use as an electrode material for supercapacitor. Specific capacitances of CA and ACA-X electrodes were measured by cyclic voltammetry and galvanostatic charge/discharge methods in 6 M KOH electrolyte. Among the samples, ACA-5 h showed the highest BET surface area (2574 m2/g) and the highest specific capacitance (100 F/g). It was found that CO2 activation was a very efficient method for enhancing physicochemical property and supercapacitive electrochemical performance of activated carbon aerogel.

  16. CO2 Activated Carbon Aerogel with Enhanced Electrochemical Performance as a Supercapacitor Electrode Material.

    PubMed

    Lee, Eo Jin; Lee, Yoon Jae; Kim, Jeong Kwon; Hong, Ung Gi; Yi, Jongheop; Yoon, Jung Rag; Song, In Kyu

    2015-11-01

    Carbon aerogel (CA) was prepared by a sol-gel polymerization of resorcinol and formaldehyde in ambient conditions. A series of activated carbon aerogels (ACA-X, X = 1, 2, 3, 4, 5, and 6 h) were then prepared by CO2 activation of CA with a variation of activation time (X) for use as an electrode material for supercapacitor. Specific capacitances of CA and ACA-X electrodes were measured by cyclic voltammetry and galvanostatic charge/discharge methods in 6 M KOH electrolyte. Among the samples, ACA-5 h showed the highest BET surface area (2574 m2/g) and the highest specific capacitance (100 F/g). It was found that CO2 activation was a very efficient method for enhancing physicochemical property and supercapacitive electrochemical performance of activated carbon aerogel. PMID:26726618

  17. Nomex-derived activated carbon fibers as electrode materials in carbon based supercapacitors

    NASA Astrophysics Data System (ADS)

    Leitner, K.; Lerf, A.; Winter, M.; Besenhard, J. O.; Villar-Rodil, S.; Suárez-García, F.; Martínez-Alonso, A.; Tascón, J. M. D.

    Electrochemical characterization has been carried out for electrodes prepared of several activated carbon fiber samples derived from poly (m-phenylene isophthalamide) (Nomex) in an aqueous solution. Depending on the burn-off due to activation the BET surface area of the carbons was in the order of 1300-2800 m 2 g -1, providing an extensive network of micropores. Their capability as active material for supercapacitors was evaluated by using cyclic voltammetry and impedance spectroscopy. Values for the capacitance of 175 F g -1 in sulfuric acid were obtained. Further on, it was observed that the specific capacitance and the performance of the electrode increase significantly with increasing burn-off degree. We believe that this fact can be attributed to the increase of surface area and porosity with increasing burn-off.

  18. End-of-life Zn-MnO2 batteries: electrode materials characterization.

    PubMed

    Cabral, Marta; Pedrosa, F; Margarido, F; Nogueira, C A

    2013-01-01

    Physical and chemical characterization of several sizes and shapes of alkaline and saline spent Zn-MnO2 batteries was carried out, aiming at contributing for a better definition of the applicable recycling processes. The characterization essays included the mass balance of the components, cathode and anode elemental analysis, the identification of zinc and manganese bearing phases and the morphology analysis of the electrode particles. The electrode materials correspond to 64-79% of the total weigh of the batteries, with the cathodes having clearly the highest contribution (usually more than 50%). The steel components, mainly from the cases, are also important (17-30%). Elemental analysis showed that the electrodes are highly concentrated in zinc (from 48-87% in anodes) and manganese (from 35-50% in cathodes). X-Ray powder diffraction allowed for identifying several phases in the electrodes, namely zinc oxide, in the anodes of all the types of saline and alkaline batteries tested, while zinc hydroxide chloride and ammine zinc chloride only appear in some types of saline batteries. The manganese found in the cathode materials is present as two main phases, MnO x Mn2O3 and ZnO x Mn2O3, the latter corroborating that zinc migration from anode to cathode occurs during the batteries lifespan. A unreacted MnO2 phase was also found presenting a low crystalline level. Leaching trials with diluted HCI solutions of alkaline and saline battery samples showed that all zinc species are reactive attaining easily over than 90% leaching yields, and about 30% of manganese, present as Mn(II/III) forms. The MnO2 phase is less reactive and requires higher temperatures to achieve a more efficient solubilization.

  19. Identification and Mitigation of Generated Solid By-Products during Advanced Electrode Materials Processing.

    PubMed

    Tsai, Candace S J; Dysart, Arthur D; Beltz, Jay H; Pol, Vilas G

    2016-03-01

    A scalable, solid-state elevated-temperature process was developed to produce high-capacity carbonaceous electrode materials for energy storage devices via decomposition of a starch-based precursor in an inert atmosphere. In a separate study, it is shown that the fabricated carbonaceous architectures are useful as an excellent electrode material for lithium-ion, sodium-ion, and lithium-sulfur batteries. This article focuses on the study and analysis of the formed nanometer-sized by-products during the lab-scale synthesis of the carbon material. The material production process was studied in operando (that is, during the entire duration of heat treatment). The unknown downstream particles in the process exhaust were collected and characterized via aerosol and liquid suspensions, and they were quantified using direct-reading instruments for number and mass concentrations. The airborne emissions were collected using the Tsai diffusion sampler (TDS) for characterization and further analysis. Released by-product aerosols collected in a deionized (DI) water trap were analyzed, and the aerosols emitted from the post-water-suspension were collected and characterized. After long-term sampling, individual particles in the nanometer size range were observed in the exhaust aerosol with layer-structured aggregates formed on the sampling substrate. Upon the characterization of the released aerosol by-products, methods were identified to mitigate possible human and environmental exposures upon industrial implementation. PMID:26716402

  20. Stepwise charging and calcination atmosphere effects for iron and nickel substituted lithium manganese oxide positive electrode material

    NASA Astrophysics Data System (ADS)

    Tabuchi, Mitsuharu; Kageyama, Hiroyuki; Shibuya, Hideka; Doumae, Kyosuke; Yuge, Ryota; Tamura, Noriyuki

    2016-05-01

    Fe- and Ni-substituted Li2MnO3 (Li1+x(FeyNiyMn1-2y)1-xO2, 0 < x < 1/3, y = 0.1, 0.15, 0.2) was prepared using coprecipitation-calcination. Its electrochemical properties were sensitive to the calcining atmosphere or the charging mode. Calcination in N2 atmosphere or selecting stepwise charging mode respectively engender better electrochemical performance than calcination in an air atmosphere or selecting galvanostatic charging mode. In fact, the sample for which y = 0.15 calcined in N2 atmosphere exhibited higher discharge capacity than that for the sample calcined in air atmosphere when stepwise charging mode was selected. By selecting stepwise charging mode instead of galvanostatic charging mode, the initial discharge capacity was increased and cyclability was improved. Among the samples calcined in N2 atmosphere, samples for which y = 0.1 and 0.15 were found to have attractive composition as positive electrode materials by selecting stepwise charging mode.

  1. Solution-based chemical synthesis of electrode materials for electrochemical power sources

    NASA Astrophysics Data System (ADS)

    Jeong, Yeon Uk

    The popularity of portable electronic devices and the desire for clean-air vehicles have created enormous interest in electrochemical power sources. Lithium-ion batteries offering higher energy density compared to other rechargeable battery systems are becoming the choice of a power source for portables. On the other hand, electrochemical supercapacitors offering higher power density compared to batteries are appealing for hybrid electric vehicles. However, both the lithium-ion and supercapacitor technologies are hampered by the high cost and toxicity of the currently used electrode materials. This dissertation explores alternate low cost materials for lithium-ion batteries and supercapacitors by employing novel solution-based chemical synthesis procedures. Manganese oxides are attractive alternates for lithium-ion cells as Mn is inexpensive and environmentally benign. Several NaxMnO 2+delta oxides crystallizing in different structures have been synthesized in this study by reducing sodium permanganate with sodium iodide in aqueous medium followed by firing the reduction product. While the hexagonal Na 0.7MnO2+delta (delta ≈ 0.3) transforms to a spinel-like phase during ion exchange with lithium salts, the layered and tunnel Na 0.5MnO2+delta are quite stable to ion-exchange reactions. The ion-exchanged layered and tunnel Na0.5-xLixMnO 2+delta exhibit initial capacities of, respectively, 225 and 170 mA/g. While it is difficult to maintain a high capacity with good cyclability with the tunnel structure, the layered material is found to exhibit good cyclability. Amorphous RuO2·xH2O has been shown in the literature to exhibit a high capacitance of 720 F/g in electrochemical redox capacitors. With an objective to lower the cost per F capacitance, (i) substitutions of low cost Cr and W for Ru, (ii) coating of RuO2·xH 2O on low cost oxides, and (iii) other low cost transition metal oxides and sulfides in various electrolytes have been pursued in this study. Ru1-xCrxO2

  2. Time-lag properties of corona streamer discharges between impulse sphere and dc needle electrodes under atmospheric air conditions

    NASA Astrophysics Data System (ADS)

    Okano, Daisuke

    2013-02-01

    In this study of corona streamer discharges from an impulse generator using a dc power supply, the relationship of the discharge time-lag with the dc bias voltage between the sphere-to-needle electrodes under atmospheric conditions is investigated. Devices utilizing corona discharges have been used to purify air or water, destroy bacteria, and to remove undesirable substances, and in order to achieve fast response times and high power efficiencies in such devices, it is important to minimize the time-lag of the corona discharge. Our experimental results show that (a) the discharge path of a negatively biased needle electrode will be straighter than that of a positively biased needle and (b) the discharge threshold voltage in both the positive and the negative needle electrodes is nearly equal to 33 kV. By expressing the discharge voltage as a power function of time-lag, the extent of corona generation can be quantitatively specified using the exponent of this power function. The observed behavior of a corona streamer discharge between the negative spherical and the positive needle electrodes indicates that the largest power exponent is associated with the shortest time-lag, owing to the reduction in the statistical time-lag in the absence of a formative time-lag.

  3. Transitions from near-surface to interior redox upon lithiation in conversion electrode materials.

    PubMed

    He, Kai; Xin, Huolin L; Zhao, Kejie; Yu, Xiqian; Nordlund, Dennis; Weng, Tsu-Chien; Li, Jing; Jiang, Yi; Cadigan, Christopher A; Richards, Ryan M; Doeff, Marca M; Yang, Xiao-Qing; Stach, Eric A; Li, Ju; Lin, Feng; Su, Dong

    2015-02-11

    Nanoparticle electrodes in lithium-ion batteries have both near-surface and interior contributions to their redox capacity, each with distinct rate capabilities. Using combined electron microscopy, synchrotron X-ray methods and ab initio calculations, we have investigated the lithiation pathways that occur in NiO electrodes. We find that the near-surface electroactive (Ni(2+) → Ni(0)) sites saturated very quickly, and then encounter unexpected difficulty in propagating the phase transition into the electrode (referred to as a "shrinking-core" mode). However, the interior capacity for Ni(2+) → Ni(0) can be accessed efficiently following the nucleation of lithiation "fingers" that propagate into the sample bulk, but only after a certain incubation time. Our microstructural observations of the transition from a slow shrinking-core mode to a faster lithiation finger mode corroborate with synchrotron characterization of large-format batteries and can be rationalized by stress effects on transport at high-rate discharge. The finite incubation time of the lithiation fingers sets the intrinsic limitation for the rate capability (and thus the power) of NiO for electrochemical energy storage devices. The present work unravels the link between the nanoscale reaction pathways and the C-rate-dependent capacity loss and provides guidance for the further design of battery materials that favors high C-rate charging.

  4. Transitions from near-surface to interior redox upon lithiation in conversion electrode materials

    SciTech Connect

    He, Kai; Xin, Huolin L.; Zhao, Kejie; Yu, Xiqian; Norlund, Dennis; Weng, Tsu-Chien; Li, Jing; Jiang, Yi; Cadigan, Christopher A.; Richards, Ryan M.; Doeff, Marca M.; Yang, Xiao-Qing; Stach, Eric A.; Li, Ju; Lin, Feng; Su, Dong

    2015-01-29

    Nanoparticle electrodes in lithium-ion batteries have both near-surface and interior contributions to their redox capacity, each with distinct rate capabilities. Using combined electron microscopy, synchrotron X-ray methods and ab initio calculations, we have investigated the lithiation pathways that occur in NiO electrodes. We find that the near-surface electroactive (Ni²⁺→Ni⁰) sites saturated very quickly, and then encounter unexpected difficulty in propagating the phase transition into the electrode (referred to as a “shrinking-core” mode). However, the interior capacity for Ni²⁺→Ni⁰ can be accessed efficiently following the nucleation of lithiation “fingers” which propagate into the sample bulk, but only after a certain incubation time. Our microstructural observations of the transition from a slow shrinking-core mode to a faster lithiation finger mode corroborate with synchrotron characterization of large-format batteries, and can be rationalized by stress effects on transport at high-rate discharge. The finite incubation time of the lithiation fingers sets the intrinsic limitation for the rate capability (and thus the power) of NiO for electrochemical energy storage devices. The present work unravels the link between the nanoscale reaction pathways and the C-rate-dependent capacity loss, and provides guidance for the further design of battery materials that favors high C-rate charging.

  5. Transitions from near-surface to interior redox upon lithiation in conversion electrode materials

    DOE PAGES

    He, Kai; Xin, Huolin L.; Zhao, Kejie; Yu, Xiqian; Norlund, Dennis; Weng, Tsu-Chien; Li, Jing; Jiang, Yi; Cadigan, Christopher A.; Richards, Ryan M.; et al

    2015-01-29

    Nanoparticle electrodes in lithium-ion batteries have both near-surface and interior contributions to their redox capacity, each with distinct rate capabilities. Using combined electron microscopy, synchrotron X-ray methods and ab initio calculations, we have investigated the lithiation pathways that occur in NiO electrodes. We find that the near-surface electroactive (Ni²⁺→Ni⁰) sites saturated very quickly, and then encounter unexpected difficulty in propagating the phase transition into the electrode (referred to as a “shrinking-core” mode). However, the interior capacity for Ni²⁺→Ni⁰ can be accessed efficiently following the nucleation of lithiation “fingers” which propagate into the sample bulk, but only after a certain incubationmore » time. Our microstructural observations of the transition from a slow shrinking-core mode to a faster lithiation finger mode corroborate with synchrotron characterization of large-format batteries, and can be rationalized by stress effects on transport at high-rate discharge. The finite incubation time of the lithiation fingers sets the intrinsic limitation for the rate capability (and thus the power) of NiO for electrochemical energy storage devices. The present work unravels the link between the nanoscale reaction pathways and the C-rate-dependent capacity loss, and provides guidance for the further design of battery materials that favors high C-rate charging.« less

  6. Material properties of the Pt electrode deposited on nafion membrane by the impregnation-reduction method.

    PubMed

    Rashid, Muhammad; Jun, Tae-Sun; Kim, Yong Shin

    2013-05-01

    Platinum nanoparticles (Pt NPs) were chemically deposited on a Nafion polymer electrolyte membrane by the impregnation-reduction (I-R) procedure to prepare an active electrode for solid electrochemical sensors. Various analysis methods such as SEM, EDX, XRD and cyclic voltammogram (CV) measurements were employed in order to characterize microstructures and electrochemical properties of the Pt layer. At the conditions ([Pt(NH3)4Cl2] = 10 mM, [NaBH4] = 60 mM, 50 degrees C), the porous Pt thin-film, consisting of sphere-like particles formed by the agglomeration of primary polycrystalline Pt NPs with an average crystal size of 13-18 nm, was obtained and confirmed to have a large surface area (roughness factor = 267) and strong adhesion due to the formation of interfacial Pt-Nafion composites. The secondary globular particles were found to have an average diameter of 215 nm and irregular protuberances on the surface. Furthermore, this electrode exhibited well-resolved CV peaks for the hydrogen redox reactions in an acid solution, suggesting the existence of different adsorption sites and good electrochemical behaviors. Pt/Nafion electrodes were prepared under different conditions in [Pt(NH3)4Cl2], [NaBH4] and reaction temperature, and their material properties were discussed from the viewpoint of a Pt growth mechanism. PMID:23858916

  7. Specific features of operation of a membrane-electrode assembly of an air-hydrogen fuel cell

    NASA Astrophysics Data System (ADS)

    Nechitailov, A. A.; Glebova, N. V.; Koshkina, D. V.; Tomasov, A. A.; Zelenina, N. K.; Terukova, E. E.

    2013-09-01

    Specific features of the operation of the membrane-electrode assembly with high catalytic activity that are a part of the simplified design of a low-temperature air-hydrogen fuel cell under conditions of forced and natural convection of air on the cathode are studied. The governing effect of water balance on the specific power of the fuel cell in the stationary mode (˜1 h) is shown, and the range of the operating conditions of the cell with self-control is determined. The power of the fuel cell at an efficiency of ˜50% and the surface density of platinum on a cathode of ≈0.2 mg/cm2 is 200-250 and 100 mW/cm2 in the forced and natural air-convection modes, respectively, which is comparable with the advanced results.

  8. 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.

  9. Penternary chalcogenides nanocrystals as catalytic materials for efficient counter electrodes in dye-synthesized solar cells

    NASA Astrophysics Data System (ADS)

    Özel, Faruk; Sarılmaz, Adem; Istanbullu, Bilal; Aljabour, Abdalaziz; Kuş, Mahmut; Sönmezoğlu, Savaş

    2016-07-01

    The penternary chalcogenides Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 were successfully synthesized by hot-injection method, and employed as a catalytic materials for efficient counter electrodes in dye-synthesized solar cells (DSSCs). The structural, compositional, morphological and optical properties of these pentenary semiconductors were characterized by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), energy-dispersive spectrometer (EDS) and ultraviolet-visible (UV–Vis) spectroscopy. The Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 nanocrystals had a single crystalline, kesterite phase, adequate stoichiometric ratio, 18–25 nm particle sizes which are forming nanospheres, and band gap energy of 1.18 and 1.45 eV, respectively. Furthermore, the electrochemical impedance spectroscopy and cyclic voltammograms indicated that Cu2CoSn(SeS)4 nanocrystals as counter electrodes exhibited better electrocatalytic activity for the reduction of iodine/iodide electrolyte than that of Cu2ZnSn(SeS)4 nanocrystals and conventional platinum (Pt). The photovoltaic results demonstrated that DSSC with a Cu2CoSn(SeS)4 nanocrystals-based counter electrode achieved the best efficiency of 6.47%, which is higher than the same photoanode employing a Cu2ZnSn(SeS)4 nanocrystals (3.18%) and Pt (5.41%) counter electrodes. These promising results highlight the potential application of penternary chalcogen Cu2CoSn(SeS)4 nanocrystals in low-cost, high-efficiency, Pt-free DSSCs.

  10. Penternary chalcogenides nanocrystals as catalytic materials for efficient counter electrodes in dye-synthesized solar cells.

    PubMed

    Özel, Faruk; Sarılmaz, Adem; İstanbullu, Bilal; Aljabour, Abdalaziz; Kuş, Mahmut; Sönmezoğlu, Savaş

    2016-01-01

    The penternary chalcogenides Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 were successfully synthesized by hot-injection method, and employed as a catalytic materials for efficient counter electrodes in dye-synthesized solar cells (DSSCs). The structural, compositional, morphological and optical properties of these pentenary semiconductors were characterized by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), energy-dispersive spectrometer (EDS) and ultraviolet-visible (UV-Vis) spectroscopy. The Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 nanocrystals had a single crystalline, kesterite phase, adequate stoichiometric ratio, 18-25 nm particle sizes which are forming nanospheres, and band gap energy of 1.18 and 1.45 eV, respectively. Furthermore, the electrochemical impedance spectroscopy and cyclic voltammograms indicated that Cu2CoSn(SeS)4 nanocrystals as counter electrodes exhibited better electrocatalytic activity for the reduction of iodine/iodide electrolyte than that of Cu2ZnSn(SeS)4 nanocrystals and conventional platinum (Pt). The photovoltaic results demonstrated that DSSC with a Cu2CoSn(SeS)4 nanocrystals-based counter electrode achieved the best efficiency of 6.47%, which is higher than the same photoanode employing a Cu2ZnSn(SeS)4 nanocrystals (3.18%) and Pt (5.41%) counter electrodes. These promising results highlight the potential application of penternary chalcogen Cu2CoSn(SeS)4 nanocrystals in low-cost, high-efficiency, Pt-free DSSCs. PMID:27380957

  11. Penternary chalcogenides nanocrystals as catalytic materials for efficient counter electrodes in dye-synthesized solar cells

    PubMed Central

    Özel, Faruk; Sarılmaz, Adem; İstanbullu, Bilal; Aljabour, Abdalaziz; Kuş, Mahmut; Sönmezoğlu, Savaş

    2016-01-01

    The penternary chalcogenides Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 were successfully synthesized by hot-injection method, and employed as a catalytic materials for efficient counter electrodes in dye-synthesized solar cells (DSSCs). The structural, compositional, morphological and optical properties of these pentenary semiconductors were characterized by X-ray diffraction (XRD), Raman spectroscopy, transmission electron microscopy (TEM), energy-dispersive spectrometer (EDS) and ultraviolet-visible (UV–Vis) spectroscopy. The Cu2CoSn(SeS)4 and Cu2ZnSn(SeS)4 nanocrystals had a single crystalline, kesterite phase, adequate stoichiometric ratio, 18–25 nm particle sizes which are forming nanospheres, and band gap energy of 1.18 and 1.45 eV, respectively. Furthermore, the electrochemical impedance spectroscopy and cyclic voltammograms indicated that Cu2CoSn(SeS)4 nanocrystals as counter electrodes exhibited better electrocatalytic activity for the reduction of iodine/iodide electrolyte than that of Cu2ZnSn(SeS)4 nanocrystals and conventional platinum (Pt). The photovoltaic results demonstrated that DSSC with a Cu2CoSn(SeS)4 nanocrystals-based counter electrode achieved the best efficiency of 6.47%, which is higher than the same photoanode employing a Cu2ZnSn(SeS)4 nanocrystals (3.18%) and Pt (5.41%) counter electrodes. These promising results highlight the potential application of penternary chalcogen Cu2CoSn(SeS)4 nanocrystals in low-cost, high-efficiency, Pt-free DSSCs. PMID:27380957

  12. Electrode including porous particles with embedded active material for use in a secondary electrochemical cell

    DOEpatents

    Vissers, Donald R.; Nelson, Paul A.; Kaun, Thomas D.; Tomczuk, Zygmunt

    1978-04-25

    Particles of carbonaceous matrices containing embedded electrode active material are prepared for vibratory loading within a porous electrically conductive substrate. In preparing the particles, active materials such as metal chalcogenides, solid alloys of alkali or alkaline earth metals along with other metals and their oxides in powdered or particulate form are blended with a thermosetting resin and particles of a volatile to form a paste mixture. The paste is heated to a temperature at which the volatile transforms into vapor to impart porosity at about the same time as the resin begins to cure into a rigid, solid structure. The solid structure is then comminuted into porous, carbonaceous particles with the embedded active material.

  13. Method of preparing porous, active material for use in electrodes of secondary electrochemical cells

    DOEpatents

    Vissers, Donald R.; Nelson, Paul A.; Kaun, Thomas D.; Tomczuk, Zygmunt

    1977-01-01

    Particles of carbonaceous matrices containing embedded electrode active material are prepared for vibratory loading within a porous electrically conductive substrate. In preparing the particles, active materials such as metal chalcogenides, solid alloys of alkali or alkaline earth metals along with other metals and their oxides in powdered or particulate form are blended with a thermosetting resin and particles of a volatile to form a paste mixture. The paste is heated to a temperature at which the volatile transforms into vapor to impart porosity at about the same time as the resin begins to cure into a rigid, solid structure.The solid structure is then comminuted into porous, carbonaceous particles with the embedded active material.

  14. 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

  15. 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.

  16. 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.

  17. 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.

  18. Effect of Structure on the Storage Characteristics of ManganeseOxide Electrode Materials

    SciTech Connect

    Park, Yong Joon; Doeff, Marca M.

    2006-01-31

    Eleven types of manganese-containing electrode materialswere subjected to long-term storage at 55oC in 1M LiPF6 ethylenecarbonate/dimethyl carbonate (EC/DMC) solutions. The amount of manganesedissolution observed depended upon the sample surface area, the averageMn oxidation state, the structure, and substitution levels of themanganese oxide. In some cases, structural changes such as solvateformation were exacerbated by the high temperature storage, andcontributed to capacity fading upon cycling even in the absence ofsignificant Mn dissolution. The most stable materials appear to beTi-substituted tunnel structures and mixed metal layered oxides with Mnin the +4 oxidation state.

  19. A blister-test apparatus for studies on the adhesion of materials used for neural electrodes.

    PubMed

    Ordonez, Juan; Boehler, Christian; Schuettler, Martin; Stieglitz, Thomas

    2011-01-01

    A blister test apparatus has been developed, which allows a quantitative adhesion analysis of thin-film metallizations on polymers manufactured in cleanroom conditions suitable for micromachining of neural electrode arrays. The device is capable of pressurizing metallic membranes at wafer level, monitoring the pressure and the height of the developing blister while detecting the moment of delamination, allowing the calculation of the adhesion energy between metal film and polymer. The machine is designed for quantitative long-term studies of materials used in neural microelectrode arrays.

  20. 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

  1. 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

  2. Comparative electrochemical studies of a nanostructured vanadium oxide electrode material in aqueous electrolyte

    NASA Astrophysics Data System (ADS)

    Soghomonian, Victoria; Yuan, Qifan; Ren, Shaola; Zukowski, Julia

    Electrochemical energy storage plays an increasing role in energy solutions. We report on a new hydrothermally synthesized vanadium oxide nanostructured material and study its performance as electrode material for insertion of various ions from aqueous solutions. The as-synthesized product is in the form of nanosheets forming quasi-spherical 3-dimensional objects. Variable temperature resistivity measurements indicate a thermally activated behavior. Electrodes are constructed, and comparative electrochemical insertion reactions of Li, Na, K and NH4 cations, over different cycle numbers, investigated. Concomitantly, morphological and microstructural changes are characterized by scanning electron microscopy, providing physical input to the observed electrochemical behavior. Specific charge is calculated. For Li and K, the specific charge decreases as the cycle number increases, while the reverse is observed for Na and NH4 cations. The trends are correlated to the morphological changes observed. The specific charge in the case of ammonium reaches 180 mAh/g after 20 cycles and continues increasing, indicating that ammonium cations may be considered as viable charge carriers for electrical energy storage system, and moreover in an aqueous electrolyte. We acknowledge support from the National Science Foundation, Grant No. DMR-1206338.

  3. Facile synthesis of birnessite-type manganese oxide nanoparticles as supercapacitor electrode materials.

    PubMed

    Liu, Lihu; Luo, Yao; Tan, Wenfeng; Zhang, Yashan; Liu, Fan; Qiu, Guohong

    2016-11-15

    Manganese oxides are environmentally benign supercapacitor electrode materials and, in particular, birnessite-type structure shows very promising electrochemical performance. In this work, nanostructured birnessite was facilely prepared by adding dropwise NH2OH·HCl to KMnO4 solution under ambient temperature and pressure. In order to fully exploit the potential of birnessite-type manganese oxide electrode materials, the effects of specific surface area, pore size, content of K(+), and manganese average oxidation state (Mn AOS) on their electrochemical performance were studied. The results showed that with the increase of NH2OH·HCl, the Mn AOS decreased and the corresponding pore sizes and specific surface area of birnessite increased. The synthesized nanostructured birnessite showed the highest specific capacitance of 245Fg(-1) at a current density of 0.1Ag(-1) within a potential range of 0-0.9V, and excellent cycle stability with a capacitance retention rate of 92% after 3000 cycles at a current density of 1.0Ag(-1). The present work implies that specific capacitance is mainly affected by specific surface area and pore volume, and provides a new method for the facile preparation of birnessite-type manganese oxide with excellent capacitive performance.

  4. Bridging Oriented Copper Nanowire-Graphene Composites for Solution-Processable, Annealing-Free, and Air-Stable Flexible Electrodes.

    PubMed

    Zhang, Wang; Yin, Zhenxing; Chun, Alvin; Yoo, Jeeyoung; Kim, Youn Sang; Piao, Yuanzhe

    2016-01-27

    One-dimensional flexible metallic nanowires (NWs) are of considerable interest for next-generation wearable devices. The unavoidable challenge for a wearable electrode is the assurance of high conductivity, flexibility, and durability with economically feasible materials and simple manufacturing processes. Here, we use a straightforward solvothermal method to prepare a flexible conductive material that contains reduced graphene oxide (RGO) nanosheets bridging oriented copper NWs. The GO-assistance route can successfully meet the criteria listed above and help the composite films maintain high conductivity and durable flexibility without any extra treatment, such as annealing or acid processes. The composite film exhibits a high electrical performance (0.808 Ω·sq(-1)) without considerable change over 30 days under ambient conditions. Moreover, the Cu NW-RGO composites can be deposited on polyester cloth as a lightweight wearable electrode with high durability and simple processability and are very promising for a wide variety of electronic devices. PMID:26720592

  5. Three-dimensional silicon/carbon core-shell electrode as an anode material for lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Kim, Jung Sub; Pfleging, Wilhelm; Kohler, Robert; Seifert, Hans Jürgen; Kim, Tae Yong; Byun, Dongjin; Jung, Hun-Gi; Choi, Wonchang; Lee, Joong Kee

    2015-04-01

    Practical application of silicon anodes for lithium-ion batteries has been mainly hindered because of their low electrical conductivity and large volume change (ca. 300%) occurring during the lithiation and delithiation processes. Thus, the surface engineering of active particles (material design) and the modification of electrode structure (electrode design) of silicon are necessary to alleviate these critical limiting factors. Silicon/carbon core-shell particles (Si@C, material design) are prepared by the thermal decomposition and subsequent three-dimensional (3D) electrode structures (electrode design) with a channel width of 15 μm are incorporated using the laser ablation process. The electrochemical characteristics of 3D Si@C used as the anode material for lithium-ion batteries are investigated to identify the effects of material and electrode design. By the introduction of a carbon coating and the laser structuring, an enhanced performance of Si anode materials exhibiting high specific capacity (>1200 mAh g-1 over 300 cycles), good rate capability (1170 mAh g-1 at 8 A g-1), and stable cycling is achieved. The morphology of the core-shell active material combined with 3D channel architecture can minimize the volume expansion by utilizing the void space during the repeated cycling.

  6. Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation

    PubMed Central

    Jewell, Eifion; Philip, Bruce; Greenwood, Peter

    2016-01-01

    Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices. PMID:27355967

  7. Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation.

    PubMed

    Jewell, Eifion; Philip, Bruce; Greenwood, Peter

    2016-06-27

    Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices.

  8. Improved Manufacturing Performance of Screen Printed Carbon Electrodes through Material Formulation.

    PubMed

    Jewell, Eifion; Philip, Bruce; Greenwood, Peter

    2016-01-01

    Printed carbon graphite materials are the primary common component in the majority of screen printed sensors. Screen printing allows a scalable manufacturing solution, accelerating the means by which novel sensing materials can make the transition from laboratory material to commercial product. A common bottleneck in any thick film printing process is the controlled drying of the carbon paste material. A study has been undertaken which examines the interaction between material solvent, printed film conductivity and process consistency. The study illustrates that it is possible to reduce the solvent boiling point to significantly increase process productivity while maintaining process consistency. The lower boiling point solvent also has a beneficial effect on the conductivity of the film, reducing the sheet resistance. It is proposed that this is a result of greater film stressing increasing charge percolation through greater inter particle contact. Simulations of material performance and drying illustrate that a multi layered printing provides a more time efficient manufacturing method. The findings have implications for the volume manufacturing of the carbon sensor electrodes but also have implications for other applications where conductive carbon is used, such as electrical circuits and photovoltaic devices. PMID:27355967

  9. 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.

  10. TOPICAL REVIEW: Electrode materials: a challenge for the exploitation of protonic solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Fabbri, Emiliana; Pergolesi, Daniele; Traversa, Enrico

    2010-08-01

    High temperature proton conductor (HTPC) oxides are attracting extensive attention as electrolyte materials alternative to oxygen-ion conductors for use in solid oxide fuel cells (SOFCs) operating at intermediate temperatures (400-700 °C). The need to lower the operating temperature is dictated by cost reduction for SOFC pervasive use. The major stake for the deployment of this technology is the availability of electrodes able to limit polarization losses at the reduced operation temperature. This review aims to comprehensively describe the state-of-the-art anode and cathode materials that have so far been tested with HTPC oxide electrolytes, offering guidelines and possible strategies to speed up the development of protonic SOFCs.

  11. Secondary Electron Emission from Dielectric Materials of a Hall Thruster with Segmented Electrodes

    SciTech Connect

    A. Dunaevsky; Y. Raitses; N.J. Fisch

    2003-02-12

    The discharge parameters in Hall thrusters depend strongly on the yield of secondary electron emission from channel walls. Comparative measurements of the yield of secondary electron emission at low energies of primary electrons were performed for several dielectric materials used in Hall thrusters with segmented electrodes. The measurements showed that at low energies of primary electrons the actual energetic dependencies of the total yield of secondary electron emission could differ from fits, which are usually used in theoretical models. The observed differences might be caused by electron backscattering, which is dominant at lower energies and depends strongly on surface properties. Fits based on power or linear laws are relevant at higher energies of primary electrons, where the bulk material properties play a decisive role.

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

    SciTech Connect

    Wilcox, James Douglas

    2008-12-01

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

  13. Niobium doped lanthanum calcium ferrite perovskite as a novel electrode material for symmetrical solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Kong, Xiaowei; Zhou, Xiaoliang; Tian, Yu; Wu, Xiaoyan; Zhang, Jun; Zuo, Wei

    2016-09-01

    Development of cost-effective and efficient electrochemical catalysts for the fuel cells electrode is of prime importance to emerging renewable energy technologies. Here, we report for the first time the novel La0.9Ca0.1Fe0.9Nb0.1O3-δ (LCFNb) perovskite with good potentiality for the electrode material of the symmetrical solid oxide fuel cells (SSOFC). The Sc0.2Zr0.8O2-δ (SSZ) electrolyte supported symmetrical cells with impregnated LCFNb and LCFNb/SDC (Ce0.8Sm0.2O2-δ) electrodes achieve relatively high power outputs with maximum power densities (MPDs) reaching up to 392 and 528.6 mW cm-2 at 850 °C in dry H2, respectively, indicating the excellent electro-catalytic activity of LCFNb towards both hydrogen oxidation and oxygen reduction. Besides, the MPDs of the symmetrical cells with LCFNb/SDC composite electrodes in CO and syngas (CO: H2 = 1:1) are almost identical to those in H2, implying that LCFNb material has similar catalytic activities to carbon monoxide compared with hydrogen. High durability in both H2, CO and syngas during the short term stability tests for 50 h are also obtained, showing desirable structure stability, and carbon deposition resistance of LCFNb based electrodes. The present results indicate that the LCFNb perovskite with remarkable cell performance is a promising electrode material for symmetrical SOFCs.

  14. Effect of bipolar electrode material on the reclamation of urban wastewater by an integrated electrodisinfection/electrocoagulation process.

    PubMed

    Llanos, Javier; Cotillas, Salvador; Cañizares, Pablo; Rodrigo, Manuel A

    2014-04-15

    This work presents an integrated electrodisinfection/electrocoagulation (ED-EC) process for urban wastewater reuse that employs iron bipolar electrodes. Boron doped diamond (BDD) was used as the anode and stainless steel (SS) as the cathode. A perforated iron plate was introduced between the anode and cathode to function as a bipolar electrode. This ED-EC combined cell makes it possible to conduct the simultaneous removal of microbiological content and elimination of turbidity from urban wastewater. The results show that current densities greater than or equal to 6.70 A m(-2) enable complete disinfection of the effluent and the removal of more than 90% of its initial turbidity. Hypochlorite and chloramines formed during the ED-EC process were found to be the main compounds responsible for the disinfection process. Furthermore, a cell configuration of cathode (inlet)-anode (outlet) improves the process performance by enhancing turbidity removal. Finally, the influence of the bipolar electrode material (iron or aluminium) was assessed. The results indicate that the efficiency of the electrodisinfection process depends mainly on the anodic material and is not influenced by the material of the bipolar electrode. In contrast, the removal of turbidity is more efficient when using iron as a bipolar electrode, especially at low current densities, due to the formation of a passive layer on the aluminium that hinders the dissolution of the bipolar electrode. PMID:24531029

  15. 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

  16. 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

  17. 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.

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

    NASA Astrophysics Data System (ADS)

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

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

  19. Performance of low cost scalable air-cathode microbial fuel cell made from clayware separator using multiple electrodes.

    PubMed

    Ghadge, Anil N; Ghangrekar, Makarand M

    2015-04-01

    Performance of scalable air-cathode microbial fuel cell (MFC) of 26 L volume, made from clayware cylinder with multiple electrodes, was evaluated. When electrodes were connected in parallel with 100 Ω resistance (R ext), power of 11.46 mW was produced which was 4.48 and 3.73 times higher than individual electrode pair and series connection, respectively. Coulombic efficiency of 5.10 ± 0.13% and chemical oxygen demand (COD) removal of 78.8 ± 5.52% was observed at R ext of 3 Ω. Performance under different organic loading rates (OLRs) varying from 0.75 to 6.0 g CODL(-1)d(-1) revealed power of 17.85 mW (47.28 mA current) at OLR of 3.0 g CODL(-1)d(-1). Internal resistance (R int) of 5.2 Ω observed is among the least value reported in literature. Long term operational stability (14 months) demonstrates the technical viability of clayware MFC for practical applications and potential benefits towards wastewater treatment and electricity recovery. PMID:25693451

  20. Electrode materials, thermal annealing sequences, and lateral/vertical phase separation of polymer solar cells from multiscale molecular simulations.

    PubMed

    Lee, Cheng-Kuang; Wodo, Olga; Ganapathysubramanian, Baskar; Pao, Chun-Wei

    2014-12-10

    The nanomorphologies of the bulk heterojunction (BHJ) layer of polymer solar cells are extremely sensitive to the electrode materials and thermal annealing conditions. In this work, the correlations of electrode materials, thermal annealing sequences, and resultant BHJ nanomorphological details of P3HT:PCBM BHJ polymer solar cell are studied by a series of large-scale, coarse-grained (CG) molecular simulations of system comprised of PEDOT:PSS/P3HT:PCBM/Al layers. Simulations are performed for various configurations of electrode materials as well as processing temperature. The complex CG molecular data are characterized using a novel extension of our graph-based framework to quantify morphology and establish a link between morphology and processing conditions. Our analysis indicates that vertical phase segregation of P3HT:PCBM blend strongly depends on the electrode material and thermal annealing schedule. A thin P3HT-rich film is formed on the top, regardless of bottom electrode material, when the BHJ layer is exposed to the free surface during thermal annealing. In addition, preferential segregation of P3HT chains and PCBM molecules toward PEDOT:PSS and Al electrodes, respectively, is observed. Detailed morphology analysis indicated that, surprisingly, vertical phase segregation does not affect the connectivity of donor/acceptor domains with respective electrodes. However, the formation of P3HT/PCBM depletion zones next to the P3HT/PCBM-rich zones can be a potential bottleneck for electron/hole transport due to increase in transport pathway length. Analysis in terms of fraction of intra- and interchain charge transports revealed that processing schedule affects the average vertical orientation of polymer chains, which may be crucial for enhanced charge transport, nongeminate recombination, and charge collection. The present study establishes a more detailed link between processing and morphology by combining multiscale molecular simulation framework with an

  1. Influence of air flow parameters on nanosecond repetitively pulsed discharges in a pin-annular electrode configuration

    NASA Astrophysics Data System (ADS)

    Heitz, Sylvain A.; Moeck, Jonas P.; Schuller, Thierry; Veynante, Denis; Lacoste, Deanna A.

    2016-04-01

    The effect of various air flow parameters on the plasma regimes of nanosecond repetitively pulsed (NRP) discharges is investigated at atmospheric pressure. The two electrodes are in a pin-annular configuration, transverse to the mean flow. The voltage pulses have amplitudes up to 15 kV, a duration of 10 ns and a repetition frequency ranging from 15 to 30 kHz. The NRP corona to NRP spark (C-S) regime transition and the NRP spark to NRP corona (S-C) regime transition are investigated for different steady and harmonically oscillating flows. First, the strong effect of a transverse flow on the C-S and S-C transitions, as reported in previous studies, is verified. Second, it is shown that the azimuthal flow imparted by a swirler does not affect the regime transition voltages. Finally, the influence of low frequency harmonic oscillations of the air flow, generated by a loudspeaker, is studied. A strong effect of frequency and amplitude of the incoming flow modulation on the NRP plasma regime is observed. Results are interpreted based on the cumulative effect of the NRP discharges and an analysis of the residence times of fluid particles in the inter-electrode region.

  2. Biochar as a sustainable electrode material for electricity production in microbial fuel cells.

    PubMed

    Huggins, Tyler; Wang, Heming; Kearns, Joshua; Jenkins, Peter; Ren, Zhiyong Jason

    2014-04-01

    Wood-based biochars were used as microbial fuel cell electrodes to significantly reduce cost and carbon footprint. The biochar was made using forestry residue (BCc) and compressed milling residue (BCp). Side-by-side comparison show the specific area of BCp (469.9m(2)g(-1)) and BCc (428.6cm(2)g(-1)) is lower than granular activated carbon (GAC) (1247.8m(2)g(-1)) but higher than graphite granule (GG) (0.44m(2)g(-1)). Both biochars showed power outputs of 532±18mWm(-2) (BCp) and 457±20mWm(-2) (BCc), comparable with GAC (674±10mWm(-2)) and GG (566±5mWm(-2)). However, lower material expenses made their power output cost 17-35US$W(-1), 90% cheaper than GAC (402US$W(-1)) or GG (392US$W(-1)). Biochar from waste also reduced the energy and carbon footprint associated with electrode manufacturing and the disposal of which could have additional agronomic benefits.

  3. Enhanced Conductivity and Electrochemical Performance of Electrode Material Based on Multifunctional Dye Doped Polypyrrole.

    PubMed

    Zang, Limin; Qiu, Jianhui; Yang, Chao; Sakai, Eiichi

    2016-03-01

    Polypyrrole were prepared via in-situ chemical oxidative polymerization in the presence of multisulfonate acid dye (acid violet 19). In this work, acid violet 19 could play the role as dopant, surfactant and physical cross-linker for pyrrole polymerization, and had impact on the morphology, dispersion stability, thermal stability, electrical conductivity and electrochemical behavior of the samples. The thermal stability of the dye doped polypyrrole was enhanced than pure polypyrrole due to the strong interactions between polypyrrole and acid violet 19. The dispersion stability of the samples in water was also improved by incorporating an appropriate amount of acid violet 19. The sample with 20% of acid violet 19 showed granular morphology with the smallest diameter of -50 nm and possessed the maximum electrical conductivity of 39.09 S/cm. The as-prepared multifunctional dye doped polypyrrole samples were used to fabricate electrodes and exhibited a mass specific capacitance of 379-206 F/g in the current density range of 0.2-1.0 A/g. The results indicated that the multifunctional dye could improve the performances of polypyrrole as electrode material for supercapacitors. PMID:27455670

  4. Activated carbon made from cow dung as electrode material for electrochemical double layer capacitor

    NASA Astrophysics Data System (ADS)

    Bhattacharjya, Dhrubajyoti; Yu, Jong-Sung

    2014-09-01

    Cow dung is one of the most abundant wastes generated on earth and has been traditionally used as fertilizer and fuel in most of the developing countries. In this study activated carbon is synthesized from cow dung by a modified chemical activation method, where partially carbonized cow dung is treated with KOH in different ratio. The synthesized activated carbon possesses irregular surface morphology with high surface area in the range of 1500-2000 m2 g-1 with proper amount of micropore and mesopore volume. In particular, we demonstrate that the surface morphology and porosity parameters change with increase in KOH ratio. These activated carbons are tested as electrode material in two-electrode symmetric supercapacitor system in non-aqueous electrolyte and found to exhibit high specific capacitance with excellent retention of it at high current density and for long term operation. In particular, the activated carbon synthesized at 2:1 ratio of KOH and the pre-carbonized char shows the best performance with specific capacitance of 124 F g-1 at 0.1 A g-1 and retains up to 117 F g-1 at 1.0 A g-1 current density. The performance is attributed to high surface area along with optimum amount of micropore and mesopore volume.

  5. 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.

  6. A novel high capacity positive electrode material with tunnel-type structure for aqueous sodium-ion batteries

    DOE PAGES

    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

  7. 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

  8. Novel Electrode Materials for Low-Temperature Solid-Oxide Fuel Cells

    SciTech Connect

    Shaowu Zha; Meilin Liu

    2005-03-23

    morphologies of the very same material is critical to the fabrication of functionally graded electrodes for solid-state electrochemical devices such as SOFCs and lithium batteries. By carefully adjusting deposition parameters, we have successfully produced oxide nano-powders with the size of 30 {approx} 200 nm. Porous films with various microstructures and morphologies are also deposited on several substrates by systematic adjustment of the deposition parameters. Highly porous, excellently bonded and nano-structured electrodes fabricated by combustion CVD exhibit extremely high surface area and remarkable catalytic activities. Using in situ potential dependent FTIR emission spectroscopy, we have found evidence for two, possibly three distinct di-oxygen species present on the electrode surface. We have successfully identified which surface oxygen species is present under a particular electrical or chemical condition and have been able to deduce the reaction mechanisms. This technique will be used to probe the gas-solid interactions at or near the TPB and on the surfaces of mixed-conducting electrodes in an effort to understand the molecular processes relevant to the intrinsic catalytic activity. Broad spectral features are assigned to the electrochemical-polarization-induced changes in the optical properties of the electrode surface layer.

  9. Novel synthesis of Ni-ferrite (NiFe{sub 2}O{sub 4}) electrode material for supercapacitor applications

    SciTech Connect

    Venkatachalam, V.; Jayavel, R.

    2015-06-24

    Novel nanocrystalline NiFe{sub 2}O{sub 4} has been synthesized through combustion route using citric acid as a fuel. Phase of the synthesized material was analyzed using powder X-ray diffraction. The XRD study revealed the formation of spinel phase cubic NiFe{sub 2}O{sub 4} with high crystallinity. The average crystallite size of NiFe{sub 2}O{sub 4} nanomaterial was calculated from scherrer equation. The electrochemical properties were realized by cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy. The electrode material shows a maximum specific capacitance of 454 F/g with pseudocapacitive behavior. High capacitance retention of electrode material over 1000 continuous charging-discharging cycles suggests its excellent electrochemical stability. The results revealed that the nickel ferrite electrode is a potential candidate for energy storage applications in supercapacitor.

  10. 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

    2014-10-14

    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.

  11. Novel synthesis of Ni-ferrite (NiFe2O4) electrode material for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Venkatachalam, V.; Jayavel, R.

    2015-06-01

    Novel nanocrystalline NiFe2O4 has been synthesized through combustion route using citric acid as a fuel. Phase of the synthesized material was analyzed using powder X-ray diffraction. The XRD study revealed the formation of spinel phase cubic NiFe2O4 with high crystallinity. The average crystallite size of NiFe2O4 nanomaterial was calculated from scherrer equation. The electrochemical properties were realized by cyclic voltammetry, chronopotentiometry and electrochemical impedance spectroscopy. The electrode material shows a maximum specific capacitance of 454 F/g with pseudocapacitive behavior. High capacitance retention of electrode material over 1000 continuous charging-discharging cycles suggests its excellent electrochemical stability. The results revealed that the nickel ferrite electrode is a potential candidate for energy storage applications in supercapacitor.

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

    NASA Astrophysics Data System (ADS)

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

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

  13. Fast fabrication of copper nanowire transparent electrodes by a high intensity pulsed light sintering technique in air.

    PubMed

    Ding, Su; Jiu, Jinting; Tian, Yanhong; Sugahara, Tohru; Nagao, Shijo; Suganuma, Katsuaki

    2015-12-14

    Copper nanowire transparent electrodes have received increasing interest due to the low price and nearly equal electrical conductivity compared with other TEs based on silver nanowires and indium tin oxide (ITO). However, a post-treatment at high temperature in an inert atmosphere or a vacuum environment was necessary to improve the conductivity of Cu NW TEs due to the easy oxidation of copper in air atmosphere, which greatly cancelled out the low price advantage of Cu NWs. Here, a high intensity pulsed light technique was introduced to sinter and simultaneously deoxygenate these Cu NWs into a highly conductive network at room temperature in air. The strong light absorption capacity of Cu NWs enabled the welding of the nanowires at contact spots, as well as the removal of the thin layer of residual organic compounds, oxides and hydroxide of copper even in air. The Cu NW TE with a sheet resistance of 22.9 Ohm sq(-1) and a transparency of 81.8% at 550 nm has been successfully fabricated within only 6 milliseconds exposure treatment, which is superior to other films treated at high temperature in a hydrogen atmosphere. The HIPL process was simple, convenient and fast to fabricate easily oxidized Cu NW TEs in large scale in an air atmosphere, which will largely extend the application of cheap Cu NW TEs.

  14. A large-area diffuse air discharge plasma excited by nanosecond pulse under a double hexagon needle-array electrode.

    PubMed

    Liu, Zhi-Jie; Wang, Wen-Chun; Yang, De-Zheng; Wang, Sen; Zhang, Shuai; Tang, Kai; Jiang, Peng-Chao

    2014-01-01

    A large-area diffuse air discharge plasma excited by bipolar nanosecond pulse is generated under a double hexagon needle-array electrode at atmospheric pressure. The images of the diffuse discharge, electric characteristics, and the optical emission spectra emitted from the diffuse air discharge plasma are obtained. Based on the waveforms of pulse voltage and current, the power consumption, and the power density of the diffuse air discharge plasma are investigated under different pulse peak voltages. The electron density and the electron temperature of the diffuse plasma are estimated to be approximately 1.42×10(11) cm(-3) and 4.4 eV, respectively. The optical emission spectra are arranged to determine the rotational and vibrational temperatures by comparing experimental with simulated spectra. Meanwhile, the rotational and vibrational temperatures of the diffuse discharge plasma are also discussed under different pulse peak voltages and pulse repetition rates, respectively. In addition, the diffuse air discharge plasma can form an area of about 70×50 mm(2) on the surface of dielectric layer and can be scaled up to the required size.

  15. Fast fabrication of copper nanowire transparent electrodes by a high intensity pulsed light sintering technique in air.

    PubMed

    Ding, Su; Jiu, Jinting; Tian, Yanhong; Sugahara, Tohru; Nagao, Shijo; Suganuma, Katsuaki

    2015-12-14

    Copper nanowire transparent electrodes have received increasing interest due to the low price and nearly equal electrical conductivity compared with other TEs based on silver nanowires and indium tin oxide (ITO). However, a post-treatment at high temperature in an inert atmosphere or a vacuum environment was necessary to improve the conductivity of Cu NW TEs due to the easy oxidation of copper in air atmosphere, which greatly cancelled out the low price advantage of Cu NWs. Here, a high intensity pulsed light technique was introduced to sinter and simultaneously deoxygenate these Cu NWs into a highly conductive network at room temperature in air. The strong light absorption capacity of Cu NWs enabled the welding of the nanowires at contact spots, as well as the removal of the thin layer of residual organic compounds, oxides and hydroxide of copper even in air. The Cu NW TE with a sheet resistance of 22.9 Ohm sq(-1) and a transparency of 81.8% at 550 nm has been successfully fabricated within only 6 milliseconds exposure treatment, which is superior to other films treated at high temperature in a hydrogen atmosphere. The HIPL process was simple, convenient and fast to fabricate easily oxidized Cu NW TEs in large scale in an air atmosphere, which will largely extend the application of cheap Cu NW TEs. PMID:26536570

  16. Few-layer MoS2-anchored graphene aerogel paper for free-standing electrode materials.

    PubMed

    Lee, Wee Siang Vincent; Peng, Erwin; Loh, Tamie Ai Jia; Huang, Xiaolei; Xue, Jun Min

    2016-04-21

    To reduce the reliance on polymeric binders, conductive additives, and metallic current collectors during the electrode preparation process, as well as to assess the true performance of lithium ion battery (LIB) anodes, a free-standing electrode has to be meticulously designed. Graphene aerogel is a popular scaffolding material that has been widely used with embedded nanoparticles for application in LIB anodes. However, the current graphene aerogel/nanoparticle composite systems still involve decomposition into powder and the addition of additives during electrode preparation because of the thick aerogel structure. To further enhance the capacity of the system, MoS2 was anchored onto a graphene aerogel paper and the composite was used directly as an LIB anode. The resultant additive-free MoS2/graphene aerogel paper composite exhibited long cyclic performance with 101.1% retention after 700 cycles, which demonstrates the importance of free-standing electrodes in enhancing cyclic stability. PMID:27020143

  17. Few-layer MoS2-anchored graphene aerogel paper for free-standing electrode materials.

    PubMed

    Lee, Wee Siang Vincent; Peng, Erwin; Loh, Tamie Ai Jia; Huang, Xiaolei; Xue, Jun Min

    2016-04-21

    To reduce the reliance on polymeric binders, conductive additives, and metallic current collectors during the electrode preparation process, as well as to assess the true performance of lithium ion battery (LIB) anodes, a free-standing electrode has to be meticulously designed. Graphene aerogel is a popular scaffolding material that has been widely used with embedded nanoparticles for application in LIB anodes. However, the current graphene aerogel/nanoparticle composite systems still involve decomposition into powder and the addition of additives during electrode preparation because of the thick aerogel structure. To further enhance the capacity of the system, MoS2 was anchored onto a graphene aerogel paper and the composite was used directly as an LIB anode. The resultant additive-free MoS2/graphene aerogel paper composite exhibited long cyclic performance with 101.1% retention after 700 cycles, which demonstrates the importance of free-standing electrodes in enhancing cyclic stability.

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

    PubMed

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

    2011-01-12

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

  19. Nano-graphite functionalized mesocellular carbon foam with enhanced intra-penetrating electrical percolation networks for high performance electrochemical energy storage electrode materials.

    PubMed

    Jo, Changshin; An, Sunhyung; Kim, Younghoon; Shim, Jongmin; Yoon, Songhun; Lee, Jinwoo

    2012-04-28

    Mesocellular carbon foam (MSU-F-C) is functionalized with hollow nanographite by a simple solution-phase method to enhance the intrapenetrating electrical percolation network. The electrical conductivity of the resulting material, denoted as MSU-F-C-G, is increased by a factor of 20.5 compared with the pristine MSU-F-C. Hollow graphite nanoparticles are well-dispersed in mesocellular carbon foam, as confirmed by transmission electron microscopy (TEM), and the d spacing of the (002) planes is 0.343 nm, which is only slightly larger than that of pure graphite (0.335 nm), suggesting a random combination of graphitic and turbostratic stacking. After nanographitic functionalization, the BET surface area and total pore volume decreased from 928 m(2) g(-1) and 1.5 cm(3) g(-1) to 394 m(2) g(-1) and 0.7 cm(3) g(-1), respectively. Thermogravimetric analysis in air shows that the thermal stability of MSU-F-C-G is improved relative to that of MSU-F-C, and the one-step weight loss indicates that the nanographite is homogeneously functionalized on the MSU-F-C particles. When the resulting mesocellular carbon materials are used as electrode materials for an electric double layer capacitor (EDLC), the specific capacitances (C(sp)) of the MSU-F-C and MSU-F-C-G electrodes at 4 mV s(-1) are 109 F g(-1) and 93 F g(-1), respectively. The MSU-F-C-G electrode exhibited a very high area capacitance (C(area), 23.5 μF cm(-2)) compared with that of the MSU-F-C electrode (11.7 μF cm(-2)), which is attributed to the enhanced intraparticle conductivity by the nanographitic functionalization. MSU-F-C-G exhibited high capacity retention (52%) at a very high scan rate of 512 mV s(-1), while only a 23% capacity retention at 512 mV s(-1) was observed in the case of the MSU-F-C electrode. When applied as an anode in a lithium ion battery, a significant increase in the initial efficiency (44%), high reversible discharge capacity (580 mA h g(-1)) in the lower voltage region, and a higher rate

  20. Nano-graphite functionalized mesocellular carbon foam with enhanced intra-penetrating electrical percolation networks for high performance electrochemical energy storage electrode materials.

    PubMed

    Jo, Changshin; An, Sunhyung; Kim, Younghoon; Shim, Jongmin; Yoon, Songhun; Lee, Jinwoo

    2012-04-28

    Mesocellular carbon foam (MSU-F-C) is functionalized with hollow nanographite by a simple solution-phase method to enhance the intrapenetrating electrical percolation network. The electrical conductivity of the resulting material, denoted as MSU-F-C-G, is increased by a factor of 20.5 compared with the pristine MSU-F-C. Hollow graphite nanoparticles are well-dispersed in mesocellular carbon foam, as confirmed by transmission electron microscopy (TEM), and the d spacing of the (002) planes is 0.343 nm, which is only slightly larger than that of pure graphite (0.335 nm), suggesting a random combination of graphitic and turbostratic stacking. After nanographitic functionalization, the BET surface area and total pore volume decreased from 928 m(2) g(-1) and 1.5 cm(3) g(-1) to 394 m(2) g(-1) and 0.7 cm(3) g(-1), respectively. Thermogravimetric analysis in air shows that the thermal stability of MSU-F-C-G is improved relative to that of MSU-F-C, and the one-step weight loss indicates that the nanographite is homogeneously functionalized on the MSU-F-C particles. When the resulting mesocellular carbon materials are used as electrode materials for an electric double layer capacitor (EDLC), the specific capacitances (C(sp)) of the MSU-F-C and MSU-F-C-G electrodes at 4 mV s(-1) are 109 F g(-1) and 93 F g(-1), respectively. The MSU-F-C-G electrode exhibited a very high area capacitance (C(area), 23.5 μF cm(-2)) compared with that of the MSU-F-C electrode (11.7 μF cm(-2)), which is attributed to the enhanced intraparticle conductivity by the nanographitic functionalization. MSU-F-C-G exhibited high capacity retention (52%) at a very high scan rate of 512 mV s(-1), while only a 23% capacity retention at 512 mV s(-1) was observed in the case of the MSU-F-C electrode. When applied as an anode in a lithium ion battery, a significant increase in the initial efficiency (44%), high reversible discharge capacity (580 mA h g(-1)) in the lower voltage region, and a higher rate

  1. The performance of La0.6Sr1.4MnO4 layered perovskite electrode material for intermediate temperature symmetrical solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Zhou, Jun; Chen, Gang; Wu, Kai; Cheng, Yonghong

    2014-12-01

    A layered perovskite electrode material, La0.6Sr1.4MnO4+δ (LSMO4), has been studied for intermediate temperature symmetrical solid oxide fuel cells (IT-SSOFCs) on La0.9Sr0.1Ga0.8Mg0.2O3-δ (LSGM) electrolyte. The chemical compatibility tests indicate that no reaction occurred between LSMO4 oxide and LSGM electrolyte at temperature up to 1000 °C both in air and 5% H2. The lower conductivity in 5% H2 and higher conduction activation energy than those in air would be caused by poorer overlap of both σ and π bonds. DFT + U calculations also show that oxygen vacancies which formed in reducing atmosphere may block the 3D hopping path for electrons or holes through Mn-O-Mn chains. For LSMO4 electrode, SEM results indicate that the electrode formed good contact with the electrolyte after being sintered at 900 °C for 2 h. At 800 °C, the polarization resistance of the LSMO4 cathode is about 0.87 Ω cm2 in air, while the polarization resistance of the LSMO4 anode is about 2.07 Ω cm2 in 5% H2. LSMO4 exhibits better electrochemical activity for oxygen reduction than that for hydrogen oxidation. A cell with LSGM electrolyte, LSMO4-LSGM mixture as anode and cathode simultaneously displays a maximum power density of 59 mW cm-2 at 800 °C.

  2. Polyaniline nanofiber/large mesoporous carbon composites as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Liu, Huan; Xu, Bin; Jia, Mengqiu; Zhang, Mei; Cao, Bin; Zhao, Xiaonan; Wang, Yu

    2015-03-01

    A composite of polyaniline nanofiber/large mesoporous carbon (PANI-F/LMC) hybrid was prepared by an in situ chemical oxidative polymerization of aniline monomer with nano-CaCO3 templated LMC as host matrix for supercapacitors. The morphology, composition and electronic structure of the composites (PANI-F/LMC) together with pure PANI nanofibers and the LMC were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), FT-IR, X-ray diffraction (XRD) and X-ray photoelectron spectroscopy (XPS). It is found that the PANI nanofibers were incorporated into the large mesochannels of LMC with interpenetrating framework formed. Such unique structure endows the PANI-F/LMC composite with a high capacitance of 473 F g-1 at a current load of 0.1 A g-1 with good rate performance and cycling stability, suggesting its potential application in the electrode material for supercapacitors.

  3. 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

  4. 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%.

  5. Few-layer MoS2-anchored graphene aerogel paper for free-standing electrode materials

    NASA Astrophysics Data System (ADS)

    Lee, Wee Siang Vincent; Peng, Erwin; Loh, Tamie Ai Jia; Huang, Xiaolei; Xue, Jun Min

    2016-04-01

    To reduce the reliance on polymeric binders, conductive additives, and metallic current collectors during the electrode preparation process, as well as to assess the true performance of lithium ion battery (LIB) anodes, a free-standing electrode has to be meticulously designed. Graphene aerogel is a popular scaffolding material that has been widely used with embedded nanoparticles for application in LIB anodes. However, the current graphene aerogel/nanoparticle composite systems still involve decomposition into powder and the addition of additives during electrode preparation because of the thick aerogel structure. To further enhance the capacity of the system, MoS2 was anchored onto a graphene aerogel paper and the composite was used directly as an LIB anode. The resultant additive-free MoS2/graphene aerogel paper composite exhibited long cyclic performance with 101.1% retention after 700 cycles, which demonstrates the importance of free-standing electrodes in enhancing cyclic stability.To reduce the reliance on polymeric binders, conductive additives, and metallic current collectors during the electrode preparation process, as well as to assess the true performance of lithium ion battery (LIB) anodes, a free-standing electrode has to be meticulously designed. Graphene aerogel is a popular scaffolding material that has been widely used with embedded nanoparticles for application in LIB anodes. However, the current graphene aerogel/nanoparticle composite systems still involve decomposition into powder and the addition of additives during electrode preparation because of the thick aerogel structure. To further enhance the capacity of the system, MoS2 was anchored onto a graphene aerogel paper and the composite was used directly as an LIB anode. The resultant additive-free MoS2/graphene aerogel paper composite exhibited long cyclic performance with 101.1% retention after 700 cycles, which demonstrates the importance of free-standing electrodes in enhancing cyclic

  6. 10 CFR 835.209 - Concentrations of radioactive material in air.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ... 10 Energy 4 2010-01-01 2010-01-01 false Concentrations of radioactive material in air. 835.209... External Exposure § 835.209 Concentrations of radioactive material in air. (a) The derived air... exposures to airborne radioactive material. (b) The estimation of internal dose shall be based on...

  7. Electrolyte optimization and electrode material evaluation for the vanadium redox battery

    NASA Astrophysics Data System (ADS)

    Kazacos, Michael

    1990-05-01

    The preparation of the electrolyte for the all vanadium redox flow battery was investigated using both chemical and electrolytic reduction of V2O5 powder. Oxalic acid and SO2 reduction were found to be unsuitable as only the V(IV) state could be produced directly. With suspended powder hydrolysis, however, vanadium sulphate of any oxidation state, in this case 50 percent V(IV) plus 50 percent V(III) in sulphuric acid can readily be prepared from V2O5 powder, thus allowing a significant reduction in the cost of the vanadium battery electrolyte. Results from conductivity and electrolyte stability tests at elevated temperature have led to modification of the electrolyte composition for the vanadium redox cell, from the 2 M V plus 2 M H2SO4, originally employed, to the use of 3 M H2SO4, much higher energy efficiencies and greater electrolyte stability was demonstrated with the 3 M H2SO4 supporting electrolyte. Spectroscopy and electrolyte conductivity were demonstrated as suitable techniques for state-of-charge monitoring. A number of electrode materials were also evaluated and a Toray graphite bonded to a carbon plastic electrode was selected for further prototype development. Energy efficiencies of between 83 and 86 percent obtained for a current density of 30 mA/sq cm for a temperature range of 5 to 45 C, and between 0 and 100 percent state-of-charge. A wide range of construction materials was tested for long term stability in the vanadium redox electrolyte.

  8. Graphene nanoplatelets with selectively functionalized edges as electrode material for electrochemical energy storage.

    PubMed

    Bhattacharjya, Dhrubajyoti; Jeon, In-Yup; Park, Hyean-Yeol; Panja, Tandra; Baek, Jong-Beom; Yu, Jong-Sung

    2015-05-26

    In recent years, graphene-based materials have been in the forefront as electrode material for electrochemical energy generation and storage. Despite this prevalent interest, synthesis procedures have not attained three important efficiency requirements, that is, cost, energy, and eco-friendliness. In this regard, in the present work, graphene nanoplatelets with selectively functionalized edges (XGnPs) are prepared through a simple, eco-friendly and efficient method, which involves ball milling of graphite in the presence of hydrogen (H2), bromine (Br2), and iodine (I2). The resultant HGnP, BrGnP, and IGnP reveal significant exfoliation of graphite layers, as evidenced by high BET surface area of 414, 595, and 772 m(2) g(-1), respectively, in addition to incorporation of H, Br, and I along with other oxygen-containing functional groups at the graphitic edges. The BrGnP and IGnP are also found to contain 4.12 and 2.20 at % of Br and I, respectively in the graphene framework. When tested as supercapacitor electrode, all XGnPs show excellent electrochemical performance in terms of specific capacitance and durability at high current density and long-term operation. Among XGnPs, IGnP delivers superior performance of 172 F g(-1) at 1 A g(-1) compared with 150 F g(-1) for BrGnP and 75 F g(-1) for HGnP because the large surface area and high surface functionality in the IGnP give rise to the outstanding capacitive performance. Moreover, all XGnPs show excellent retention of capacitance at high current density of 10 A g(-1) and for long-term operation up to 1000 charge-discharge cycles.

  9. Impedance spectroscopic analysis of composite electrode from activated carbon/conductive materials/ruthenium oxide for supercapacitor applications

    SciTech Connect

    Taer, E.; Awitdrus,; Farma, R.; Deraman, M. Talib, I. A.; Ishak, M. M.; Omar, R.; Dolah, B. N. M.; Basri, N. H.; Othman, M. A. R.; Kanwal, S.

    2015-04-16

    Activated carbon powders (ACP) were produced from the KOH treated pre-carbonized rubber wood sawdust. Different conductive materials (graphite, carbon black and carbon nanotubes (CNTs)) were added with a binder (polivinylidene fluoride (PVDF)) into ACP to improve the supercapacitive performance of the activated carbon (AC) electrodes. Symmetric supercapacitor cells, fabricated using these AC electrodes and 1 molar H{sub 2}SO{sub 4} electrolyte, were analyzed using a standard electrochemical impedance spectroscopy technique. The addition of graphite, carbon black and CNTs was found effective in reducing the cell resistance from 165 to 68, 23 and 49 Ohm respectively, and increasing the specific capacitance of the AC electrodes from 3 to 7, 17, 32 F g{sup −1} respectively. Since the addition of CNTs can produce the highest specific capacitance, CNTs were chosen as a conductive material to produce AC composite electrodes that were added with 2.5 %, 5 % and 10 % (by weight) electro-active material namely ruthenium oxide; PVDF binder and CNTs contents were kept at 5 % by weight in each AC composite produced. The highest specific capacitance of the cells obtained in this study was 86 F g{sup −1}, i.e. for the cell with the resistance of 15 Ohm and composite electrode consists of 5 % ruthenium oxide.

  10. Impedance spectroscopic analysis of composite electrode from activated carbon/conductive materials/ruthenium oxide for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Taer, E.; Deraman, M.; Talib, I. A.; Awitdrus, Farma, R.; Ishak, M. M.; Omar, R.; Dolah, B. N. M.; Basri, N. H.; Othman, M. A. R.; Kanwal, S.

    2015-04-01

    Activated carbon powders (ACP) were produced from the KOH treated pre-carbonized rubber wood sawdust. Different conductive materials (graphite, carbon black and carbon nanotubes (CNTs)) were added with a binder (polivinylidene fluoride (PVDF)) into ACP to improve the supercapacitive performance of the activated carbon (AC) electrodes. Symmetric supercapacitor cells, fabricated using these AC electrodes and 1 molar H2SO4 electrolyte, were analyzed using a standard electrochemical impedance spectroscopy technique. The addition of graphite, carbon black and CNTs was found effective in reducing the cell resistance from 165 to 68, 23 and 49 Ohm respectively, and increasing the specific capacitance of the AC electrodes from 3 to 7, 17, 32 F g-1 respectively. Since the addition of CNTs can produce the highest specific capacitance, CNTs were chosen as a conductive material to produce AC composite electrodes that were added with 2.5 %, 5 % and 10 % (by weight) electro-active material namely ruthenium oxide; PVDF binder and CNTs contents were kept at 5 % by weight in each AC composite produced. The highest specific capacitance of the cells obtained in this study was 86 F g-1, i.e. for the cell with the resistance of 15 Ohm and composite electrode consists of 5 % ruthenium oxide.

  11. Synthesis of an organic conductive porous material using starch aerogels as template for chronic invasive electrodes.

    PubMed

    Starbird, Ricardo; García-González, Carlos A; Smirnova, Irina; Krautschneider, Wolfgang H; Bauhofer, Wolfgang

    2014-04-01

    We report the development of an organic conducting mesoporous material, as coat for invasive electrodes, by a novel methodology based on the use of starch aerogel as template. The poly(3,4-ethylenedioxythiophene) (PEDOT) aerogel was synthesized by polymerization of 3,4-ethylenedioxythiophene within a saturated starch aerogel with iron (III) p-toluenesulfonate (oxidizing agent) and subsequent removal of the polysaccharide template, followed by supercritical CO2 drying. The chemical structure and oxidation state of the resulting material were studied by Raman spectroscopy. The morphology and surface properties of the obtained nanoporous material were investigated by scanning electron microscopy (SEM), micro computed tomography (μCT) and nitrogen adsorption-desorption techniques. The composition and thermal behaviour were evaluated by energy dispersive spectroscopy (EDS) and thermogravimetric analysis (TGA) respectively. A preliminary biocompatibility test verified the non-cytotoxic effects of the PEDOT aerogel. The large surface area and wide pore size distribution of the PEDOT conductive aerogel, along with its electrical properties, enable it to be used as extracellular matrix scaffold for biomedical applications.

  12. Evaluation of Niobium as Candidate Electrode Material for DC High Voltage Photoelectron Guns

    NASA Technical Reports Server (NTRS)

    BastaniNejad, M.; Mohamed, Abdullah; Elmustafa, A. A.; Adderley, P.; Clark, J.; Covert, S.; Hansknecht, J.; Hernandez-Garcia, C.; Poelker, M.; Mammei, R.; Surles-Law, K.; Williams, P.

    2012-01-01

    The field emission characteristics of niobium electrodes were compared to those of stainless steel electrodes using a DC high voltage field emission test apparatus. A total of eight electrodes were evaluated: two 304 stainless steel electrodes polished to mirror-like finish with diamond grit and six niobium electrodes (two single-crystal, two large-grain, and two fine-grain) that were chemically polished using a buffered-chemical acid solution. Upon the first application of high voltage, the best large-grain and single-crystal niobium electrodes performed better than the best stainless steel electrodes, exhibiting less field emission at comparable voltage and field strength. In all cases, field emission from electrodes (stainless steel and/or niobium) could be significantly reduced and sometimes completely eliminated, by introducing krypton gas into the vacuum chamber while the electrode was biased at high voltage. Of all the electrodes tested, a large-grain niobium electrode performed the best, exhibiting no measurable field emission (< 10 pA) at 225 kV with 20 mm cathode/anode gap, corresponding to a field strength of 18:7 MV/m.

  13. Laboratory-scale testing of non-consumable anode materials: Inert Electrodes Program

    SciTech Connect

    Marschman, S.C.

    1989-03-01

    Development of inert anode materials for use in the electrolytic production of aluminum is one of the major goals of the Inert Electrodes Program sponsored by the US Department of Energy, Office of Industrial Programs, at Pacific Northwest Laboratory. The objectives of the Materials Development and Testing Task include the selection, fabrication, and evaluation of candidate non-consumable anode materials. Research performed in FY 1987 focused primarily on the development and evaluation of cermets that are based on the two-phase oxide system NiO/endash/NiFe/sub 2/O/sub 4/ and contain a third, electrically conductive metal phase composed primarily of copper and nickel. The efforts of this task were focused on three areas: materials fabrication, small-scale materials testing, and laboratory-scale testing. This report summarizes the development and testing results of the laboratory-scale testing effort during FY 1987. The laboratory-scale electrolysis testing effort was instrumental in partially determining electrolysis cell operating parameters. Although not optimized, NiO/endash/NiFe/sub 2/O/sub 4//endash/Cu-based cermets were successfully operated for 20 h in cryolite-based electrolytes ranging in bath ratios from 1.1 to 1.35, in electrolytes that contained 1.5 wt % LiF, and at conditions slightly less than Al/sub 2/O/sub 3/ saturation. The operating conditions that lead to anode degradation have been partly identified, and rudimentary control methods have been developed to ensure proper operation of small electrolysis cells using nonconsumable anodes. 11 figs., 1 tab.

  14. Amorphous carbon nitride as an alternative electrode material in electroanalysis: simultaneous determination of dopamine and ascorbic acid.

    PubMed

    Medeiros, Roberta A; Matos, Roberto; Benchikh, Abdelkader; Saidani, Boualem; Debiemme-Chouvy, Catherine; Deslouis, Claude; Rocha-Filho, Romeu C; Fatibello-Filho, Orlando

    2013-10-01

    Boron-doped diamond (BDD) films are excellent electrode materials, whose electrochemical activity for some analytes can be tuned by controlling their surface termination, most commonly either to predominantly hydrogen or oxygen. This tuning can be accomplished by e.g. suitable cathodic or anodic electrochemical pretreatments. Recently, it has been shown that amorphous carbon nitride (a-CNx) films may present electrochemical characteristics similar to those of BDD, including the influence of surface termination on their electrochemical activity toward some analytes. In this work, we report for the first time a complete electroanalytical method using an a-CNx electrode. Thus, an a-CNx film deposited on a stainless steel foil by DC magnetron sputtering is proposed as an alternative electrode for the simultaneous determination of dopamine (DA) and ascorbic acid (AA) in synthetic biological samples by square-wave voltammetry. The obtained results are compared with those attained using a BDD electrode. For both electrodes, a same anodic pretreatment in 0.1 mol L(-1) KOH was necessary to attain an adequate and equivalent separation of the DA and AA oxidation potential peaks of about 330 mV. The detection limits obtained for the simultaneous determination of these analytes using the a-CNx electrode were 0.0656 μmol L(-1) for DA and 1.05 μmol L(-1) for AA, whereas with the BDD electrode these values were 0.283 μmol L(-1) and 0.968 μmol L(-1), respectively. Furthermore, the results obtained in the analysis of the analytes in synthetic biological samples were satisfactory, attesting the potential application of the a-CNx electrode in electroanalysis.

  15. Lactose electroisomerization into lactulose: effect of the electrode material, active membrane surface area-to-electrode surface area ratio, and interelectrode-membrane distance.

    PubMed

    Aït-Aissa, Amara; Aïder, Mohammed

    2014-01-01

    The aim of the present work was to study and develop an innovative, clean, and environmentally friendly process for lactulose synthesis by electroactivation of lactose. In this work, the electrode material (type 304 stainless steel, titanium, and copper), dimensionless interelectrode-membrane distance at the cathodic compartment (0.36, 0.68, and 1), and the membrane:electrode surface area ratio (0.23, 0.06, and 0.015) were considered to be the factors that could affect the kinetic conversion of lactose into lactulose. The reactions were conducted under an initial lactose concentration of 0.15mol/L at 10°C, Froude number (mixing speed) of 2.05×10(-2), and electric current intensity of 300mA for 30min. The highest lactulose formation yield of 32.50% (0.05mol/L) was obtained by using a copper electrode, interelectrode-membrane distance of 0.36, and membrane:electrode surface area ratio of 0.23. The 2-parameter Langmuir, Freundlich, and Temkin isotherm models were used for the prediction of the lactose isomerization kinetics as well as the 3-parameter Langmuir-Freundlich isotherm model. It was shown that the lactose isomerization kinetics into lactulose followed the Temkin and Langmuir-Freundlich models with coefficients of determination of 0.99 and 0.90 and a relative error of 1.42 to 1.56% and 4.27 to 4.37%, respectively. PMID:24931526

  16. Synthesis of NiMnO3/C nano-composite electrode materials for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Kakvand, Pejman; Safi Rahmanifar, Mohammad; El-Kady, Maher F.; Pendashteh, Afshin; Kiani, Mohammad Ali; Hashami, Masumeh; Najafi, Mohsen; Abbasi, Ali; Mousavi, Mir F.; Kaner, Richard B.

    2016-08-01

    Demand for high-performance energy storage materials has motivated research activities to develop nano-engineered composites that benefit from both high-rate and high-capacitance materials. Herein, NiMnO3 (NMO) nanoparticles have been synthesized through a facile co-precipitation method. As-prepared NMO samples are then employed for the synthesis of nano-composites with graphite (Gr) and reduced graphene oxide (RGO). Various samples, including pure NMO, NMO-graphite blend, as well as NMO/Gr and NMO/RGO nano-composites have been electrochemically investigated as active materials in supercapacitors. The NMO/RGO sample exhibited a high specific capacitance of 285 F g-1 at a current density of 1 A g-1, much higher than the other samples (237 F g-1 for NMO/Gr, 170 F g-1 for NMO-Gr and 70 F g-1 for NMO). Moreover, the NMO/RGO nano-composite has shown excellent cycle stability with a 93.5% capacitance retention over 1000 cycles at 2 A g-1 and still delivered around 87% of its initial capacitance after cycling for 4000 cycles. An NMO/RGO composite was assessed in practical applications by assembling NMO/RGO//NMO/RGO symmetric devices, exhibiting high specific energy (27.3 Wh kg-1), high specific power (7.5 kW kg-1), and good cycle stability over a broad working voltage of 1.5 V. All the obtained results demonstrate the promise of NMO/RGO nano-composite as a high-performance electrode material for supercapacitors.

  17. Synthesis of NiMnO3/C nano-composite electrode materials for electrochemical capacitors.

    PubMed

    Kakvand, Pejman; Rahmanifar, Mohammad Safi; El-Kady, Maher F; Pendashteh, Afshin; Kiani, Mohammad Ali; Hashami, Masumeh; Najafi, Mohsen; Abbasi, Ali; Mousavi, Mir F; Kaner, Richard B

    2016-08-01

    Demand for high-performance energy storage materials has motivated research activities to develop nano-engineered composites that benefit from both high-rate and high-capacitance materials. Herein, NiMnO3 (NMO) nanoparticles have been synthesized through a facile co-precipitation method. As-prepared NMO samples are then employed for the synthesis of nano-composites with graphite (Gr) and reduced graphene oxide (RGO). Various samples, including pure NMO, NMO-graphite blend, as well as NMO/Gr and NMO/RGO nano-composites have been electrochemically investigated as active materials in supercapacitors. The NMO/RGO sample exhibited a high specific capacitance of 285 F g(-1) at a current density of 1 A g(-1), much higher than the other samples (237 F g(-1) for NMO/Gr, 170 F g(-1) for NMO-Gr and 70 F g(-1) for NMO). Moreover, the NMO/RGO nano-composite has shown excellent cycle stability with a 93.5% capacitance retention over 1000 cycles at 2 A g(-1) and still delivered around 87% of its initial capacitance after cycling for 4000 cycles. An NMO/RGO composite was assessed in practical applications by assembling NMO/RGO//NMO/RGO symmetric devices, exhibiting high specific energy (27.3 Wh kg(-1)), high specific power (7.5 kW kg(-1)), and good cycle stability over a broad working voltage of 1.5 V. All the obtained results demonstrate the promise of NMO/RGO nano-composite as a high-performance electrode material for supercapacitors.

  18. Synthesis of NiMnO3/C nano-composite electrode materials for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Kakvand, Pejman; Safi Rahmanifar, Mohammad; El-Kady, Maher F.; Pendashteh, Afshin; Kiani, Mohammad Ali; Hashami, Masumeh; Najafi, Mohsen; Abbasi, Ali; Mousavi, Mir F.; Kaner, Richard B.

    2016-08-01

    Demand for high-performance energy storage materials has motivated research activities to develop nano-engineered composites that benefit from both high-rate and high-capacitance materials. Herein, NiMnO3 (NMO) nanoparticles have been synthesized through a facile co-precipitation method. As-prepared NMO samples are then employed for the synthesis of nano-composites with graphite (Gr) and reduced graphene oxide (RGO). Various samples, including pure NMO, NMO-graphite blend, as well as NMO/Gr and NMO/RGO nano-composites have been electrochemically investigated as active materials in supercapacitors. The NMO/RGO sample exhibited a high specific capacitance of 285 F g‑1 at a current density of 1 A g‑1, much higher than the other samples (237 F g‑1 for NMO/Gr, 170 F g‑1 for NMO-Gr and 70 F g‑1 for NMO). Moreover, the NMO/RGO nano-composite has shown excellent cycle stability with a 93.5% capacitance retention over 1000 cycles at 2 A g‑1 and still delivered around 87% of its initial capacitance after cycling for 4000 cycles. An NMO/RGO composite was assessed in practical applications by assembling NMO/RGO//NMO/RGO symmetric devices, exhibiting high specific energy (27.3 Wh kg‑1), high specific power (7.5 kW kg‑1), and good cycle stability over a broad working voltage of 1.5 V. All the obtained results demonstrate the promise of NMO/RGO nano-composite as a high-performance electrode material for supercapacitors.

  19. Synthesis of NiMnO3/C nano-composite electrode materials for electrochemical capacitors.

    PubMed

    Kakvand, Pejman; Rahmanifar, Mohammad Safi; El-Kady, Maher F; Pendashteh, Afshin; Kiani, Mohammad Ali; Hashami, Masumeh; Najafi, Mohsen; Abbasi, Ali; Mousavi, Mir F; Kaner, Richard B

    2016-08-01

    Demand for high-performance energy storage materials has motivated research activities to develop nano-engineered composites that benefit from both high-rate and high-capacitance materials. Herein, NiMnO3 (NMO) nanoparticles have been synthesized through a facile co-precipitation method. As-prepared NMO samples are then employed for the synthesis of nano-composites with graphite (Gr) and reduced graphene oxide (RGO). Various samples, including pure NMO, NMO-graphite blend, as well as NMO/Gr and NMO/RGO nano-composites have been electrochemically investigated as active materials in supercapacitors. The NMO/RGO sample exhibited a high specific capacitance of 285 F g(-1) at a current density of 1 A g(-1), much higher than the other samples (237 F g(-1) for NMO/Gr, 170 F g(-1) for NMO-Gr and 70 F g(-1) for NMO). Moreover, the NMO/RGO nano-composite has shown excellent cycle stability with a 93.5% capacitance retention over 1000 cycles at 2 A g(-1) and still delivered around 87% of its initial capacitance after cycling for 4000 cycles. An NMO/RGO composite was assessed in practical applications by assembling NMO/RGO//NMO/RGO symmetric devices, exhibiting high specific energy (27.3 Wh kg(-1)), high specific power (7.5 kW kg(-1)), and good cycle stability over a broad working voltage of 1.5 V. All the obtained results demonstrate the promise of NMO/RGO nano-composite as a high-performance electrode material for supercapacitors. PMID:27324723

  20. Ionic Liquid Directed Mesoporous Carbon Nanoflakes as an Effiencient Electrode material.

    PubMed

    Kong, Lirong; Chen, Wei

    2015-12-10

    Supercapacitors are considered to be the most promising approach to meet the pressing requirements for energy storage devices. The electrode materials for supercapacitors have close relationship with their electrochemical properties and thus become the key point to improve their energy storage efficiency. Herein, by using poly (vinylidene fluoride-co-hexafluoropropylene) and ionic liquid as the dual templates, polyacrylonitrile as the carbon precursor, a flake-like carbon material was prepared by a direct carbonization method. In this method, poly (vinylidene fluoride-co-hexafluoropropylene) worked as the separator for the formation of isolated carbon flakes while aggregated ionic liquid worked as the pore template. The obtained carbon flakes exhibited a specific capacitance of 170 F/g at 0.1 A/g, a high energy density of 12.2 Wh/kg and a high power density of 5 kW/kg at the current of 10 A/g. It also maintained a high capacitance retention capability with almost no declination after 500 charge-discharge cycles. The ionic liquid directed method developed here also provided a new idea for the preparation of hierarchically porous carbon nanomaterials.

  1. Hexagonal CeO2 nanostructures: an efficient electrode material for supercapacitors.

    PubMed

    Maheswari, Nallappan; Muralidharan, Gopalan

    2016-09-28

    Cerium oxide (CeO2) has emerged as a new and promising pseudocapacitive material due to its prominent valance states and extensive applications in various fields. In the present study, hexagonal CeO2 nanostructures have been prepared via the hydrothermal method employing cationic surfactant cetyl trimethyl ammonium bromide (CTAB). CTAB ensures a slow rate of hydrolysis to form small sized CeO2 nanostructures. The role of calcination temperature on the morphological, structural, electrochemical properties and cyclic stability has been assessed for supercapacitor applications. The mesoscopic hexagonal architecture endows the CeO2 with not only a higher specific capacity, but also with an excellent rate capability and cyclability. When the charge/discharge current density is increased from 2 to 10 A g(-1) the reversible charge capacity decreased from 927 F g(-1) to 475 F g(-1) while 100% capacity retention at a high current density of 20 A g(-1) even after 1500 cycles could be achieved. Furthermore, the asymmetric supercapacitor based on CeO2 exhibited a significantly higher energy density of 45.6 W h kg(-1) at a power density of 187.5 W kg(-1) with good cyclic stability. The electrochemical richness of the CeO2 nanostructure makes it a suitable electrode material for supercapacitor applications.

  2. Sodium titanate nanotubes as negative electrode materials for sodium-ion capacitors.

    PubMed

    Yin, Jiao; Qi, Li; Wang, Hongyu

    2012-05-01

    The lithium-based energy storage technology is currently being considered for electric automotive industry and even electric grid storage. However, the hungry demand for vast energy sources in the modern society will conflict with the shortage of lithium resources on the earth. The first alternative choice may be sodium-related materials. Herein, we propose an electric energy storage system (sodium-ion capacitor) based on porous carbon and sodium titanate nanotubes (Na-TNT, Na(+)-insertion compounds) as positive and negative electrode materials, respectively, in conjunction with Na(+)-containing non-aqueous electrolytes. As a low-voltage (0.1-2 V) sodium insertion nanomaterial, Na-TNT was synthesized via a simple hydrothermal reaction. Compared with bulk sodium titanate, the predominance of Na-TNT is the excellent rate performance, which exactly caters to the need for electrochemical capacitors. The sodium-ion capacitors exhibited desirable energy density and power density (34 Wh kg(-1), 889 W kg(-1)). Furthermore, the sodium-ion capacitors had long cycling life (1000 cycles) and high coulombic efficiency (≈ 98 % after the second cycle). More importantly, the conception of sodium-ion capacitor has been put forward.

  3. The Production and Characterization of Ceramic Carbon Electrode Materials for CuCl-HCl Electrolysis

    NASA Astrophysics Data System (ADS)

    Edge, Patrick

    Current H2 gas supplies are primarily produced through steam methane reforming and other fossil fuel based processes. This lack of viable large scale and environmentally friendly H2 gas production has hindered the wide spread adoption of H2 fuel cells. A potential solution to this problem is the Cu-Cl hybrid thermochemical cycle. The cycle captures waste heat to drive two thermochemical steps creating CuCl as well as O2 gas and HCl from CuCl2 and water. The CuCl is oxidized in HCl to produce H2 gas and regenerate CuCl2, this process occurs at potentials well below those required for water electrolysis. The electrolysis process occurs in a traditional PEM fuel-cell. In the aqueous anolyte media Cu(I) will form anionic complexes such as CuCl 2 - or CuCl32-. The slow transport of these species to the anode surface limits the overall electrolysis process. To improve this transport process we have produced ceramic carbon electrode (CCE) materials through a sol-gel method incorporating a selection of amine containing silanes with increasing numbers of primary and secondary amines. When protonated these amines allow for improved transport of anionic copper complexes. The electrochemical and physical characterization of these CCE materials in a half and full-cell electrolysis environment will be presented. Electrochemical analysis was performed using cell polarization, cyclic voltammetry, and electrochemical impedance spectroscopy.

  4. Kinetic modelling of molten carbonate fuel cells: Effects of cathode water and electrode materials

    NASA Astrophysics Data System (ADS)

    Arato, E.; Audasso, E.; Barelli, L.; Bosio, B.; Discepoli, G.

    2016-10-01

    Through previous campaigns the authors developed a semi-empirical kinetic model to describe MCFC performance for industrial and laboratory simulation. Although effective in a wide range of operating conditions, the model was validated for specific electrode materials and dry feeding cathode compositions. The new aim is to prove that with appropriate improvements it is possible to apply the model to MCFC provided by different suppliers and to new sets of reactant gases. Specifically, this paper describes the procedures to modify the model to switch among different materials and identify a new parameter taking into account the effects of cathode water vapour. The new equation is integrated as the kinetic core within the SIMFC (SIMulation of Fuel Cells) code, an MCFC 3D model set up by the PERT group of the University of Genova, for reliability test. Validation is performed using data collected through tests carried out at the University of Perugia using single cells. The results are discussed giving examples of the simulated performance with varying operating conditions. The final formulation average percentage error obtained for all the simulated cases with respect to experimental results is maintained around 1%, despite the difference between the basic and the new conditions and facilities.

  5. Ionic Liquid Directed Mesoporous Carbon Nanoflakes as an Effiencient Electrode material

    PubMed Central

    Kong, Lirong; Chen, Wei

    2015-01-01

    Supercapacitors are considered to be the most promising approach to meet the pressing requirements for energy storage devices. The electrode materials for supercapacitors have close relationship with their electrochemical properties and thus become the key point to improve their energy storage efficiency. Herein, by using poly (vinylidene fluoride-co-hexafluoropropylene) and ionic liquid as the dual templates, polyacrylonitrile as the carbon precursor, a flake-like carbon material was prepared by a direct carbonization method. In this method, poly (vinylidene fluoride-co-hexafluoropropylene) worked as the separator for the formation of isolated carbon flakes while aggregated ionic liquid worked as the pore template. The obtained carbon flakes exhibited a specific capacitance of 170 F/g at 0.1 A/g, a high energy density of 12.2 Wh/kg and a high power density of 5 kW/kg at the current of 10 A/g. It also maintained a high capacitance retention capability with almost no declination after 500 charge-discharge cycles. The ionic liquid directed method developed here also provided a new idea for the preparation of hierarchically porous carbon nanomaterials. PMID:26656464

  6. An Approach to Preparing Ni-P with Different Phases for Use as Supercapacitor Electrode Materials.

    PubMed

    Wang, Dan; Kong, Ling-Bin; Liu, Mao-Cheng; Luo, Yong-Chun; Kang, Long

    2015-12-01

    Herein, we describe a simple two-step approach to prepare nickel phosphide with different phases, such as Ni2 P and Ni5 P4 , to explain the influence of material microstructure and electrical conductivity on electrochemical performance. In this approach, we first prepared a Ni-P precursor through a ball milling process, then controlled the synthesis of either Ni2 P or Ni5 P4 by the annealing method. The as-prepared Ni2 P and Ni5 P4 are investigated as supercapacitor electrode materials for potential energy storage applications. The Ni2 P exhibits a high specific capacitance of 843.25 F g(-1) , whereas the specific capacitance of Ni5 P4 is 801.5 F g(-1) . Ni2 P possesses better cycle stability and rate capability than Ni5 P4 . In addition, the Fe2 O3 //Ni2 P supercapacitor displays a high energy density of 35.5 Wh kg(-1) at a power density of 400 W kg(-1) and long cycle stability with a specific capacitance retention rate of 96 % after 1000 cycles, whereas the Fe2 O3 //Ni5 P4 supercapacitor exhibits a high energy density of 29.8 Wh kg(-1) at a power density of 400 W kg(-1) and a specific capacitance retention rate of 86 % after 1000 cycles. PMID:26477441

  7. Development of a Northern Continental Air Standard Reference Material.

    PubMed

    Rhoderick, George C; Kitzis, Duane R; Kelley, Michael E; Miller, Walter R; Hall, Bradley D; Dlugokencky, Edward J; Tans, Pieter P; Possolo, Antonio; Carney, Jennifer

    2016-03-15

    The National Institute of Standards and Technology (NIST) recently began to develop standard mixtures of greenhouse gases as part of a broad program mandated by the 2009 United States Congress to support research in climate change. To this end, NIST developed suites of gravimetrically assigned primary standard mixtures (PSMs) comprising carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-natural air balance at ambient mole fraction levels. In parallel, the National Oceanic and Atmospheric Administration (NOAA) in Boulder, Colorado, charged 30 aluminum gas cylinders with northern hemisphere air at Niwot Ridge, Colorado. These mixtures, which constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSMs. NOAA-assigned values are also provided as information in support of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Program for CO2, CH4, and N2O, since NOAA serves as the WMO Central Calibration Laboratory (CCL) for CO2, CH4, and N2O. Relative expanded uncertainties at the 95% confidence interval are <±0.06% of the certified values for CO2 and N2O and <0.2% for CH4, which represents the smallest relative uncertainties specified to date for a gaseous SRM produced by NIST. Agreement between the NOAA (WMO/GAW) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and 0.06% for CO2, CH4, and N2O, respectively. This collaborative development effort also represents the first of its kind for a gaseous SRM developed by NIST. PMID:26890890

  8. Development of a Northern Continental Air Standard Reference Material.

    PubMed

    Rhoderick, George C; Kitzis, Duane R; Kelley, Michael E; Miller, Walter R; Hall, Bradley D; Dlugokencky, Edward J; Tans, Pieter P; Possolo, Antonio; Carney, Jennifer

    2016-03-15

    The National Institute of Standards and Technology (NIST) recently began to develop standard mixtures of greenhouse gases as part of a broad program mandated by the 2009 United States Congress to support research in climate change. To this end, NIST developed suites of gravimetrically assigned primary standard mixtures (PSMs) comprising carbon dioxide (CO2), methane (CH4), and nitrous oxide (N2O) in a dry-natural air balance at ambient mole fraction levels. In parallel, the National Oceanic and Atmospheric Administration (NOAA) in Boulder, Colorado, charged 30 aluminum gas cylinders with northern hemisphere air at Niwot Ridge, Colorado. These mixtures, which constitute NIST Standard Reference Material (SRM) 1720 Northern Continental Air, were certified by NIST for ambient mole fractions of CO2, CH4, and N2O relative to NIST PSMs. NOAA-assigned values are also provided as information in support of the World Meteorological Organization (WMO) Global Atmosphere Watch (GAW) Program for CO2, CH4, and N2O, since NOAA serves as the WMO Central Calibration Laboratory (CCL) for CO2, CH4, and N2O. Relative expanded uncertainties at the 95% confidence interval are <±0.06% of the certified values for CO2 and N2O and <0.2% for CH4, which represents the smallest relative uncertainties specified to date for a gaseous SRM produced by NIST. Agreement between the NOAA (WMO/GAW) and NIST values based on their respective calibration standards suites is within 0.05%, 0.13%, and 0.06% for CO2, CH4, and N2O, respectively. This collaborative development effort also represents the first of its kind for a gaseous SRM developed by NIST.

  9. Iron-Air Rechargeable Battery

    NASA Technical Reports Server (NTRS)

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

    2014-01-01

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

  10. Influence Of Adsorbent Materials On Streamers Propagation In Air And Induced Chemical Efficiency

    NASA Astrophysics Data System (ADS)

    Guaitella, O.; Marinov, I.; Dong, B.; Rousseau, A.

    2010-07-01

    Atmospheric pressure plasmas are now used in many different applications from odor treatment to biomedicine as well as surface functionalization or molecules synthesis. Dielectric barrier discharge (DBD) is a widely used source for this application because of safety reasons, low energetic cost, and randomly distributed treatment over the whole reac- tor volume (Kogelschatz 2003, Kim 2004, Roth et al. 1998, Guaitella et al. 2008). DBD used for air treatment of volatile organic compounds (VOC) produce filamentary plasmas which have to be combined with porous catalytic surfaces. Filaments have then to ramp in contact with a complex dielectric surface, or even go through small diameter holes which could constraint the filaments. As a consequence, the breakdown, and the development of the filaments could be strongly modified by the surface, and the species adsorbed on it. The aim of this work is to discriminate in the plasma/catalyst coupling performed for VOC abatement in DBD, what is a consequence of surface chemistry on the adsorbent ma- terial from what is due to modifications of filaments behavior. The same dielectric surfaces (pyrex, quartz, TiO2 and Al2O3) are then used in different experimental setups. A classical study on VOC removal is first performed downstream a DBD with or without catalyst. These results are compared to surface chemistry directly measured onto the surfaces by DRIFT method. Then, the physical properties of filaments generated on the same surfaces are analyzed with three different experiments. A double electrode surface DBD discharge allows studying the influence of photo-desorption of charges stored onto the surface on the filament breakdown. Then the dynamic of charge deposition is obtained by electrical measurement on a devoted multiple ground electrodes reactor. Finally, the velocity and electric field are measured for air streamers forced to propagate inside capillary tube. All these experiments performed with the same dielectric

  11. Generation of large-scale, barrier-free diffuse plasmas in air at atmospheric pressure using array wire electrodes and nanosecond high-voltage pulses

    NASA Astrophysics Data System (ADS)

    Teng, Yun; Li, Lee; Liu, Yun-Long; Liu, Lun; Liu, Minghai

    2014-10-01

    This paper introduces a method to generate large-scale diffuse plasmas by using a repetition nanosecond pulse generator and a parallel array wire-electrode configuration. We investigated barrier-free diffuse plasmas produced in the open air in parallel and cross-parallel array line-line electrode configurations. We found that, when the distance between the wire-electrode pair is small, the discharges were almost extinguished. Also, glow-like diffuse plasmas with little discharge weakening were obtained in an appropriate range of line-line distances and with a cathode-grounding cross-electrode configuration. As an example, we produced a large-scale, stable diffuse plasma with volumes as large as 18 × 15 × 15 cm3, and this discharge region can be further expanded. Additionally, using optical and electrical measurements, we showed that the electron temperature was higher than the gas temperature, which was almost the same as room temperature. Also, an array of electrode configuration with more wire electrodes had helped to prevent the transition from diffuse discharge to arc discharge. Comparing the current waveforms of configurations with 1 cell and 9 cells, we found that adding cells significantly increased the conduction current and the electrical energy delivered in the electrode gaps.

  12. Generation of large-scale, barrier-free diffuse plasmas in air at atmospheric pressure using array wire electrodes and nanosecond high-voltage pulses

    SciTech Connect

    Teng, Yun; Li, Lee Liu, Yun-Long; Liu, Lun; Liu, Minghai

    2014-10-15

    This paper introduces a method to generate large-scale diffuse plasmas by using a repetition nanosecond pulse generator and a parallel array wire-electrode configuration. We investigated barrier-free diffuse plasmas produced in the open air in parallel and cross-parallel array line-line electrode configurations. We found that, when the distance between the wire-electrode pair is small, the discharges were almost extinguished. Also, glow-like diffuse plasmas with little discharge weakening were obtained in an appropriate range of line-line distances and with a cathode-grounding cross-electrode configuration. As an example, we produced a large-scale, stable diffuse plasma with volumes as large as 18 × 15 × 15 cm{sup 3}, and this discharge region can be further expanded. Additionally, using optical and electrical measurements, we showed that the electron temperature was higher than the gas temperature, which was almost the same as room temperature. Also, an array of electrode configuration with more wire electrodes had helped to prevent the transition from diffuse discharge to arc discharge. Comparing the current waveforms of configurations with 1 cell and 9 cells, we found that adding cells significantly increased the conduction current and the electrical energy delivered in the electrode gaps.

  13. Development of Novel Electrode Materials for the Electrocatalysis of Oxygen-Transfer and Hydrogen-Transfer Reactions

    SciTech Connect

    Brett Kimball Simpson

    2002-08-27

    Throughout this thesis, the fundamental aspects involved in the electrocatalysis of anodic O-transfer reactions and cathodic H-transfer reactions have been studied. The investigation into anodic O-transfer reactions at undoped and Fe(III)[doped MnO{sub 2} films] revealed that MnO{sub 2} film electrodes prepared by a cycling voltammetry deposition show improved response for DMSO oxidation at the film electrodes vs. the Au substrate. Doping of the MnO{sub 2} films with Fe(III) further enhanced electrode activity. Reasons for this increase are believed to involve the adsorption of DMSO by the Fe(III) sites. The investigation into anodic O-transfer reactions at undoped and Fe(III)-doped RuO{sub 2} films showed that the Fe(III)-doped RuO{sub 2}-film electrodes are applicable for anodic detection of sulfur compounds. The Fe(III) sites in the Fe-RuO{sub 2} films are speculated to act as adsorption sites for the sulfur species while the Ru(IV) sites function for anodic discharge of H{sub 2}O to generate the adsorbed OH species. The investigation into cathodic H-transfer reactions, specifically nitrate reduction, at various pure metals and their alloys demonstrated that the incorporation of metals into alloy materials can create a material that exhibits bifunctional properties for the various steps involved in the overall nitrate reduction reaction. The Sb{sub 10}Sn{sub 20}Ti{sub 70}, Cu{sub 63}Ni{sub 37} and Cu{sub 25}Ni{sub 75} alloy electrodes exhibited improved activity for nitrate reduction as compared to their pure component metals. The Cu{sub 63}Ni{sub 37} alloy displayed the highest activity for nitrate reduction. The final investigation was a detailed study of the electrocatalytic activity of cathodic H-transfer reactions (nitrate reduction) at various compositions of Cu-Ni alloy electrodes. Voltammetric response for NO{sub 3}{sup -} at the Cu-Ni alloy electrode is superior to the response at the pure Cu and Ni electrodes. This is explained on the basis of the

  14. Novel shielding materials for space and air travel.

    PubMed

    Vana, N; Hajek, M; Berger, T; Fugger, M; Hofmann, P

    2006-01-01

    The reduction of dose onboard spacecraft and aircraft by appropriate shielding measures plays an essential role in the future development of space exploration and air travel. The design of novel shielding strategies and materials may involve hydrogenous composites, as it is well known that liquid hydrogen is most effective in attenuating charged particle radiation. As precursor for a later flight experiment, the shielding properties of newly developed hydrogen-rich polymers and rare earth-doped high-density rubber were tested in various ground-based neutron and heavy ion fields and compared with aluminium and polyethylene as reference materials. Absorbed dose, average linear energy transfer and gamma-equivalent neutron absorbed dose were determined by means of LiF:Mg,Ti thermoluminescence dosemeters and CR-39 plastic nuclear track detectors. First results for samples of equal aerial density indicate that selected hydrogen-rich plastics and rare-earth-doped rubber may be more effective in attenuating cosmic rays by up to 10% compared with conventional aluminium shielding. The appropriate adaptation of shielding thicknesses may thus allow reducing the biologically relevant dose. Owing to the lower density of the plastic composites, mass savings shall result in a significant reduction of launch costs. The experiment was flown as part of the European Space Agency's Biopan-5 mission in May 2005.

  15. A novel high capacity positive electrode material with tunnel-type structure for aqueous sodium-ion batteries

    SciTech Connect

    Wang, Yuesheng; Mu, Linqin; Liu, Jue; Yang, Zhenzhong; Yu, Xiqian; Gu, Lin; Hu, Yong -Sheng; Li, Hong; Yang, Xiao -Qing; Chen, Liquan; Huang, Xuejie

    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. 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.

  16. 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.

  17. Studies on supercapacitor electrode material from activated lignin-derived mesoporous carbon.

    PubMed

    Saha, Dipendu; Li, Yunchao; Bi, Zhonghe; Chen, Jihua; Keum, Jong K; Hensley, Dale K; Grappe, Hippolyte A; Meyer, Harry M; Dai, Sheng; Paranthaman, M Parans; Naskar, A K

    2014-01-28

    We synthesized mesoporous carbon from pre-cross-linked lignin gel impregnated with a surfactant as the pore-forming agent and then activated the carbon through physical and chemical methods to obtain activated mesoporous carbon. The activated mesoporous carbons exhibited 1.5- to 6-fold increases in porosity with a maximum Brunauer-Emmett-Teller (BET) specific surface area of 1148 m(2)/g and a pore volume of 1.0 cm(3)/g. Both physical and chemical activation enhanced the mesoporosity along with significant microporosity. Plots of cyclic voltammetric data with the capacitor electrode made from these carbons showed an almost rectangular curve depicting the behavior of ideal double-layer capacitance. Although the pristine mesoporous carbon exhibited a range of surface-area-based capacitance similar to that of other known carbon-based supercapacitors, activation decreased the surface-area-based specific capacitance and enhanced the gravimetric specific capacitance of the mesoporous carbons. A vertical tail in the lower-frequency domain of the Nyquist plot provided additional evidence of good supercapacitor behavior for the activated mesoporous carbons. We have modeled the equivalent circuit of the Nyquist plot with the help of two constant phase elements (CPE). Our work demonstrated that biomass-derived mesoporous carbon materials continue to show potential for use in specific electrochemical applications.

  18. Studies on Supercapacitor Electrode Material from Activated Lignin-Derived Mesoporous Carbon

    SciTech Connect

    Saha, Dipendu; Li, Yunchao; Bi, Zhonghe; Chen, Jihua; Keum, Jong Kahk; Hensley, Dale K; Grappe, Hippolyte A.; Meyer III, Harry M; Dai, Sheng; Paranthaman, Mariappan Parans; Naskar, Amit K

    2014-01-01

    We synthesized mesoporous carbon from pre-cross-linked lignin gel impregnated with a surfactant as the pore-forming agent, and then activated the carbon through physical and chemical methods to obtain activated mesoporous carbon. The activated mesoporous carbons exhibited 1.5- to 6-fold increases in porosity with a maximum BET specific surface area of 1148 m2/g and a pore volume of 1.0 cm3/g. Slow physical activation helped retain dominant mesoporosity; however, aggressive chemical activation caused some loss of the mesopore volume fraction. Plots of cyclic voltammetric data with the capacitor electrode made from these carbons showed an almost rectangular curve depicting the behavior of ideal double-layer capacitance. Although the pristine mesoporous carbon exhibited the same range of surface-area-based capacitance as that of other known carbon-based supercapacitors, activation decreased the surface-area-based specific capacitance and increased the gravimetric-specific capacitance of the mesoporous carbons. Surface activation lowered bulk density and electrical conductivity. Warburg impedance as a vertical tail in the lower frequency domain of Nyquist plots supported good supercapacitor behavior for the activated mesoporous carbons. Our work demonstrated that biomass-derived mesoporous carbon materials continue to show potential for use in specific electrochemical applications.

  19. Understanding sodium versus lithium intercalation potentials of electrode materials for alkali-ion batteries

    NASA Astrophysics Data System (ADS)

    Arroyo-de Dompablo, M. Elena

    2014-08-01

    Differences in average voltages for the alkali ion intercalation (Li, Na) in a variety of electrode materials are investigated. The average Li and Na insertion potentials in the cavities of ◻ReO3-perovskite, ramsdellite-◻Ti2O4, layered-◻2A2Ti3O7 (A = Li, Na) and NASICON-◻Na3Ti2(PO4)3 have been calculated by first principles calculations at the density functional theory level. The results identify the type of site occupied by the inserted ion as the relevant structural parameter. Occupation of large sites (c.n. = 12, 8) might yield Na insertion voltages higher than Li ones. On the other extreme, occupation of tetrahedral sites raises the Li insertion voltage as much as 0.8 V above the Na one. For octahedral sites the higher polarizing character of Li ions vs. Na ions acts as a key-factor to bring the Li intercalation voltage above that of Na intercalation.

  20. Sensitive determination of carbendazim in orange juice by electrode modified with hybrid material.

    PubMed

    Razzino, Claudia A; Sgobbi, Lívia F; Canevari, Thiago C; Cancino, Juliana; Machado, Sergio A S

    2015-03-01

    This paper describes the application of a glassy carbon electrode modified with a thin film of mesoporous silica/multiwalled carbon nanotubes for voltammetric determination of the fungicide carbendazim (CBZ). The hybrid material, (SiO2/MWCNT), was obtained by a sol-gel process using HF as the catalyst. The amperometric response to CBZ was measured at +0.73 V vs. Ag/AgCl by square wave voltammetry at pH 8.0. SiO2/MWCNT/GCE responded to CBZ in the linear range from 0.2 to 4.0 μmol L(-1). The calculated detection limit was 0.056 μmol L(-1), obtained using statistical methods. The SiO2/MWCNT/GCE sensor presented as the main characteristics high sensitivity, low detection limit and robustness, allowing CBZ determination in untreated real samples. In addition, this strategy afforded remarkable selectivity for CBZ against ascorbic and citric acid which are the main compounds of the orange juice. The excellent sensitivity and selectivity yielded feasible application for CBZ detection in orange juice sample.

  1. Solid Liquid Interdiffusion Bonding of Zn4Sb3 Thermoelectric Material with Cu Electrode

    NASA Astrophysics Data System (ADS)

    Lin, Y. C.; Lee, K. T.; Hwang, J. D.; Chu, H. S.; Hsu, C. C.; Chen, S. C.; Chuang, T. H.

    2016-10-01

    The ZnSb intermetallic compound may have thermoelectric applications because it is low in cost and environmentally friendly. In this study, a Zn4Sb3 thermoelectric element coated with a Ni barrier layer and a Ag reaction layer was bonded with a Ag-coated Cu electrode using a Ag/Sn/Ag solid-liquid interdiffusion bonding process. The results indicated that a Ni5Zn21 intermetallic phase formed easily at the Zn4Sb3/Ni interface, leading to sound adhesion. In addition, Sn film was found to react completely with the Ag layer to form a Ag3Sn intermetallic layer having a melting point of 480°C. The resulting Zn4Sb3 thermoelectric module can be applied at the optimized operation temperature (400°C) of Zn4Sb3 material as a thermoelectric element. The bonding strengths ranged from 14.9 MPa to 25.0 MPa, and shear tests revealed that the Zn4Sb3/Cu-joints fractured through the interior of the thermoelectric elements.

  2. Electrochemical Properties of Graphene Oxide/Resol Composites as Electrode Materials for Supercapacitor Applications.

    PubMed

    Park, Geon Woo; Jeon, Sang Kwon; Yang, Jin Yong; Choi, Sung Dae; Kim, Geon Joong

    2016-05-01

    RGO/Resol carbon composites were prepared from a mixture of reduced GO and a low-molecular-weight phenolic resin (Resol) solution. The effects of the calcination temperature, amount of Resol added and KOH treatment on the electrochemical performance of the RGO/Resol composites were investigated. The physical and electrochemical properties of the composite materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET) surface areas measurements, and cyclic voltammetry (CV). The relationships between their physical properties and their electrochemical performance were examined for use as super-capacitors (SCs). The RGO/Resol composite calcined at 400 degrees C after the KOH loading showed dramatically improved electrochemical properties, showing a high BET surface and capacitance of 2190 m2/g and 220 F/g, respectively. The RGO/Resol composites calcined after the KOH treatment showed much better capacitor performance than those treated only thermally at the same temperature without KOH impregnation. The fabrication of high surface electrodes was essential for improving the SCs properties. PMID:27483752

  3. Effect of the graphite electrode material on the characteristics of molten salt electrolytically produced carbon nanomaterials

    SciTech Connect

    Kamali, Ali Reza Schwandt, Carsten; Fray, Derek J.

    2011-10-15

    The electrochemical erosion of a graphite cathode during the electrolysis of molten lithium chloride salt may be used for the preparation of nano-structured carbon materials. It has been found that the structures and morphologies of these carbon nanomaterials are dependent on those of the graphite cathodes employed. A combination of tubular and spherical carbon nanostructures has been produced from a graphite with a microstructure of predominantly planar micro-sized grains and a minor fraction of more irregular nano-sized grains, whilst only spherical carbon nanostructures have been produced from a graphite with a microstructure of primarily nano-sized grains. Based on the experimental results, a best-fit regression equation is proposed that relates the crystalline domain size of the graphite reactants and the carbon products. The carbon nanomaterials prepared possess a fairly uniform mesoporosity with a sharp peak in pore size distribution at around 4 nm. The results are of crucial importance to the production of carbon nanomaterials by way of the molten salt electrolytic method. - Highlights: {yields} Carbon nanomaterials are synthesised by LiCl electrolysis with graphite electrodes. {yields} The degree of crystallinity of graphite reactant and carbon product are related. {yields} A graphite reactant is identified that enables the preparation of carbon nanotubes. {yields} The carbon products possess uniform mesoporosity with narrow pore size distribution.

  4. Electrochemical Properties of Graphene Oxide/Resol Composites as Electrode Materials for Supercapacitor Applications.

    PubMed

    Park, Geon Woo; Jeon, Sang Kwon; Yang, Jin Yong; Choi, Sung Dae; Kim, Geon Joong

    2016-05-01

    RGO/Resol carbon composites were prepared from a mixture of reduced GO and a low-molecular-weight phenolic resin (Resol) solution. The effects of the calcination temperature, amount of Resol added and KOH treatment on the electrochemical performance of the RGO/Resol composites were investigated. The physical and electrochemical properties of the composite materials were characterized by scanning electron microscopy (SEM), X-ray diffraction (XRD), Brunauer, Emmett and Teller (BET) surface areas measurements, and cyclic voltammetry (CV). The relationships between their physical properties and their electrochemical performance were examined for use as super-capacitors (SCs). The RGO/Resol composite calcined at 400 degrees C after the KOH loading showed dramatically improved electrochemical properties, showing a high BET surface and capacitance of 2190 m2/g and 220 F/g, respectively. The RGO/Resol composites calcined after the KOH treatment showed much better capacitor performance than those treated only thermally at the same temperature without KOH impregnation. The fabrication of high surface electrodes was essential for improving the SCs properties.

  5. Solid Liquid Interdiffusion Bonding of Zn4Sb3 Thermoelectric Material with Cu Electrode

    NASA Astrophysics Data System (ADS)

    Lin, Y. C.; Lee, K. T.; Hwang, J. D.; Chu, H. S.; Hsu, C. C.; Chen, S. C.; Chuang, T. H.

    2016-06-01

    The ZnSb intermetallic compound may have thermoelectric applications because it is low in cost and environmentally friendly. In this study, a Zn4Sb3 thermoelectric element coated with a Ni barrier layer and a Ag reaction layer was bonded with a Ag-coated Cu electrode using a Ag/Sn/Ag solid-liquid interdiffusion bonding process. The results indicated that a Ni5Zn21 intermetallic phase formed easily at the Zn4Sb3/Ni interface, leading to sound adhesion. In addition, Sn film was found to react completely with the Ag layer to form a Ag3Sn intermetallic layer having a melting point of 480°C. The resulting Zn4Sb3 thermoelectric module can be applied at the optimized operation temperature (400°C) of Zn4Sb3 material as a thermoelectric element. The bonding strengths ranged from 14.9 MPa to 25.0 MPa, and shear tests revealed that the Zn4Sb3/Cu-joints fractured through the interior of the thermoelectric elements.

  6. Borophene as an extremely high capacity electrode material for Li-ion and Na-ion batteries.

    PubMed

    Zhang, Xiaoming; Hu, Junping; Cheng, Yingchun; Yang, Hui Ying; Yao, Yugui; Yang, Shengyuan A

    2016-08-18

    "Two-dimensional (2D) materials as electrodes" is believed to be the trend for future Li-ion and Na-ion battery technologies. Here, by using first-principles methods, we predict that the recently reported borophene (2D boron sheets) can serve as an ideal electrode material with high electrochemical performance for both Li-ion and Na-ion batteries. The calculations are performed on two experimentally stable borophene structures, namely β12 and χ3 structures. The optimized Li and Na adsorption sites are identified, and the host materials are found to maintain good electric conductivity before and after adsorption. Besides advantages including small diffusion barriers and low average open-circuit voltages, most remarkably, the storage capacity can be as high as 1984 mA h g(-1) in β12 borophene and 1240 mA h g(-1) in χ3 borophene for both Li and Na, which are several times higher than the commercial graphite electrode and are the highest among all the 2D materials discovered to date. Our results highly support that borophenes can be appealing anode materials for both Li-ion and Na-ion batteries with extremely high power density. PMID:27502997

  7. Effect of electrode geometry on high energy spark discharges in air

    NASA Astrophysics Data System (ADS)

    Belmouss, Mounia

    The government, aerospace, and transportation industries are deeply invested in developing new technologies to improve the performance and maneuverability of current and future aircraft while reducing aerodynamic noise and environmental impact. One of the key pathways to meet these goals is through aerodynamic flow control, which can involve suppressing or inducing separation, transition and management of turbulence in boundary layers, increasing the lift and reducing the drag of airfoils, and gas mixing to control fluctuating forces and aerodynamic noise [1]. In this dissertation, the complex flow field following a spark discharge is studied for a range of geometries and discharge characteristics, and the possibilities for using the induced flow for aerodynamic control are assessed. This work shows the influence of the electrode configuration on the fluid dynamics following the spark discharge and how the hot gas evolution gives rise to various physical phenomena (i.e. generation of turbulence, inducing vorticity, and gas mixing) that can be used to modify the flow-field structure near the boundary layer on an aerodynamic surface.

  8. An adhesive conducting electrode material based on commercial mesoporous titanium dioxide as a support for Horseradish peroxidase for bioelectrochemical applications.

    PubMed

    Rahemi, Vanoushe; Trashin, Stanislav; Meynen, Vera; De Wael, Karolien

    2016-01-01

    An adhesive conducting electrode material containing of graphite, biocompatible ion exchange polymer nafion(®) and commercial mesoporous TiO2 impregnated with horseradish peroxidase (HRP) is prepared and characterized by amperometric, UV-vis and N2 sorption methods. The factors influencing the performance of the resulting biosensor are studied in detail. The optimal electrode material consists of 45% graphite, 50% impregnated HRP-TiO2 and 5% nafion(®). The optimum conditions for H2O2 reduction are an applied potential of -0.3 V and 0.1 mM hydroquinone. Sensitivity and limit of detection in the optimum conditions are 1 A M(-1) cm(-2) and 1 µM correspondingly. The N2 sorption results show that the pore volume of TiO2 decreases sharply upon adsorption of HRP. The preparation process of the proposed enzyme electrode is straightforward and potentially can be used for preparation of carbon paste electrodes for bioelectrochemical detections. PMID:26695318

  9. Highly Flexible Freestanding Porous Carbon Nanofibers for Electrodes Materials of High-Performance All-Carbon Supercapacitors.

    PubMed

    Liu, Ying; Zhou, Jinyuan; Chen, Lulu; Zhang, Peng; Fu, Wenbin; Zhao, Hao; Ma, Yufang; Pan, Xiaojun; Zhang, Zhenxing; Han, Weihua; Xie, Erqing

    2015-10-28

    Highly flexible porous carbon nanofibers (P-CNFs) were fabricated by electrospining technique combining with metal ion-assistant acid corrosion process. The resultant fibers display high conductivity and outstanding mechanical flexibility, whereas little change in their resistance can be observed under repeatedly bending, even to 180°. Further results indicate that the improved flexibility of P-CNFs can be due to the high graphitization degree caused by Co ions. In view of electrode materials for high-performance supercapacitors, this type of porous nanostructure and high graphitization degree could synergistically facilitate the electrolyte ion diffusion and electron transportation. In the three electrodes testing system, the resultant P-CNFs electrodes can exhibit a specific capacitance of 104.5 F g(-1) (0.2 A g(-1)), high rate capability (remain 56.5% at 10 A g(-1)), and capacitance retention of ∼94% after 2000 cycles. Furthermore, the assembled symmetric supercapacitors showed a high flexibility and can deliver an energy density of 3.22 Wh kg(-1) at power density of 600 W kg(-1). This work might open a way to improve the mechanical properties of carbon fibers and suggests that this type of freestanding P-CNFs be used as effective electrode materials for flexible all-carbon supercapacitors.

  10. Bioelectricity generation in continuously-fed microbial fuel cell: effects of anode electrode material and hydraulic retention time.

    PubMed

    Akman, Dilek; Cirik, Kevser; Ozdemir, Sebnem; Ozkaya, Bestamin; Cinar, Ozer

    2013-12-01

    The main aim of this study is to investigate the bioelectricity production in continuously-fed dual chambered microbial fuel cell (MFC). Initially, MFC was operated with different anode electrode material at constant hydraulic retention time (HRT) of 2d to evaluate the effect of electrode material on electricity production. Pt electrode yielded about 642 mW/m(2) power density, which was 4 times higher than that of the MFC with the mixed metal oxide titanium (Ti-TiO2). Further, MFC equipped with Pt electrode was operated at varying HRT (2-0.5d). The power density generation increased with decreasing HRT, corresponding to 1313 mW/m(2) which was maximum value obtained during this study. Additionally, decreasing HRT from 2 to 0.5d resulted in increasing effluent dissolved organic carbon (DOC) concentration from 1.92 g/L to 2.23 g/L, corresponding to DOC removal efficiencies of 46% and 38%, respectively.

  11. Impedance spectroscopy study of a catechol-modified activated carbon electrode as active material in electrochemical capacitor

    NASA Astrophysics Data System (ADS)

    Cougnon, C.; Lebègue, E.; Pognon, G.

    2015-01-01

    Modified activated carbon (Norit S-50) electrodes with electrochemical double layer (EDL) capacitance and redox capacitance contributions to the electric charge storage were tested in 1 M H2SO4 to quantify the benefit and the limitation of the surface redox reactions on the electrochemical performances of the resulting pseudo-capacitive materials. The electrochemical performances of an electrochemically anodized carbon electrode and a catechol-modified carbon electrode, which make use both EDL capacitance of the porous structure of the carbon and redox capacitance, were compared to the performances obtained for the pristine carbon. Nitrogen gas adsorption measurements have been used for studying the impact of the grafting on the BET surface area, pore size distribution, pore volume and average pore diameter. The electrochemical behavior of carbon materials was studied by cyclic voltammetry and electrochemical impedance spectroscopy (EIS). The EIS data were discussed by using a complex capacitance model that allows defining the characteristic time constant, the global capacitance and the frequency at which the maximum charge stored is reached. The EIS measurements were achieved at different dc potential values where a redox activity occurs and the evolution of the capacitance and the capacitive relaxation time with the electrode potential are presented. Realistic galvanostatic charge/discharge measurements performed at different current rates corroborate the results obtained by impedance.

  12. Screening of Novel Li-Air Battery Catalyst Materials by a Thin Film Combinatorial Materials Approach.

    PubMed

    Hauck, John G; McGinn, Paul J

    2015-06-01

    A combinatorial synthesis and high-throughput screening process was developed for the investigation of potential oxygen reduction reaction (ORR) and oxygen evolution reaction (OER) catalysts for use as Li-air battery cathode materials. Libraries of discrete ternary metal alloy compositions were deposited via thin-film sputtering. The samples were electrochemically tested in parallel using cyclic voltammetry in O2-saturated KOH electrolyte. Compositions were ranked by ORR and OER onset potentials with respect to an internal Pt reference. Results from the Pt-Mn-Co, Cr-Mn-Co, Pd-Mn-Co, and Pd-Mn-Ru systems are reported. Many alloy compositions showed marked improvement in catalytic activity compared to pure Pt. Among the systems considered, Pt12Mn44Co44, Pd43Co57 and Pd36Mn28Ru36 in particular exhibited lower overpotentials for oxygen reactions, which occur at the cathode in Li-air batteries.

  13. Rapid synthesis of monodispersed highly porous spinel nickel cobaltite (NiCo2O4) electrode material for supercapacitors

    NASA Astrophysics Data System (ADS)

    Naveen, A. Nirmalesh; Selladurai, S.

    2015-06-01

    Monodispersed highly porous spinel nickel cobaltite electrode material was successfully synthesized in a short time using combustion technique. Single phase cubic nature of the spinel nickel cobaltite with average crystallite size of 24 nm was determined from X-ray diffraction study. Functional groups present in the compound were determined from FTIR study and it further confirms the spinel formation. FESEM images reveal the porous nature of the prepared material and uniform size distribution of the particles. Electrochemical evaluation was performed using Cyclic Voltammetry (CV) technique, Chronopotentiometry (CP) and Electrochemical Impedance Spectroscopy (EIS). Results reveal the typical pseudocapacitive behaviour of the material. Maximum capacitance of 754 F/g was calculated at the scan rate of 5 mV/s, high capacitance was due to the unique porous morphology of the electrode. Nyquist plot depicts the low resistance and good electrical conductivity of nickel cobaltite. It has been found that nickel cobaltite prepared by this typical method will be a potential electrode material for supercapcitor application.

  14. Nanostructured carbon materials based electrothermal air pump actuators

    NASA Astrophysics Data System (ADS)

    Liu, Qing; Liu, Luqi; Kuang, Jun; Dai, Zhaohe; Han, Jinhua; Zhang, Zhong

    2014-05-01

    Actuator materials can directly convert different types of energy into mechanical energy. In this work, we designed and fabricated electrothermal air pump-type actuators by utilization of various nanostructured carbon materials, including single wall carbon nanotubes (SWCNTs), reduced graphene oxide (r-GO), and graphene oxide (GO)/SWCNT hybrid films as heating elements to transfer electrical stimulus into thermal energy, and finally convert it into mechanical energy. Both the actuation displacement and working temperature of the actuator films show the monotonically increasing trend with increasing driving voltage within the actuation process. Compared with common polymer nanocomposites based electrothermal actuators, our actuators exhibited better actuation performances with a low driving voltage (<10 V), large generated stress (tens of MPa), high gravimetric density (tens of J kg-1), and short response time (few hundreds of milliseconds). Besides that, the pump actuators exhibited excellent stability under cyclic actuation tests. Among these actuators, a relatively larger actuation strain was obtained for the r-GO film actuator due to the intrinsic gas-impermeability nature of graphene platelets. In addition, the high modulus of the r-GO and GO/SWCNT films also guaranteed the large generated stress and high work density. Specifically, the generated stress and gravimetric work density of the GO/SWCNT hybrid film actuator could reach up to more than 50 MPa and 30 J kg-1, respectively, under a driving voltage of 10 V. The resulting stress value is at least two orders of magnitude higher than that of natural muscles (~0.4 MPa).Actuator materials can directly convert different types of energy into mechanical energy. In this work, we designed and fabricated electrothermal air pump-type actuators by utilization of various nanostructured carbon materials, including single wall carbon nanotubes (SWCNTs), reduced graphene oxide (r-GO), and graphene oxide (GO)/SWCNT hybrid

  15. HSPES membrane electrode assembly

    NASA Technical Reports Server (NTRS)

    Kindler, Andrew (Inventor); Yen, Shiao-Ping (Inventor)

    2000-01-01

    An improved fuel cell electrode, as well as fuel cells and membrane electrode assemblies that include such an electrode, in which the electrode includes a backing layer having a sintered layer thereon, and a non-sintered free-catalyst layer. The invention also features a method of forming the electrode by sintering a backing material with a catalyst material and then applying a free-catalyst layer.

  16. The impedance response of LaY2Ni9 negative electrode materials after activation

    NASA Astrophysics Data System (ADS)

    Boussami, S.; Khaldi, C.; Lamloumi, J.; Mathlouthi, H.; Takenouti, H.; Vivier, V.

    2013-10-01

    The electrochemical impedance responses of the LaY2Ni9 alloy electrode after activation at different states of charge (SOC), immersion time in 7 M KOH and room temperature was studied. Electrochemical impedance spectrum of the metal hydride electrode obtained was interpreted by an equivalent circuit modeling including the different electrochemical processes taking place on the interface between the MH electrode and the electrolyte. The results indicate that the electrochemical reaction activity of hydride electrode was markedly enhanced with increasing state of charge. The hydrogen diffuses in the bulk of the alloy and this process is not the limiting step for the hydrogen absorption. During a long immersion time a continuous nanocrystalline corrosion scale appears and the modification of passive film toward more organized structure is concluded.

  17. Beneficial effects of air inclusions on the performance of ethylene vinyl acetate (EVA) mouthguard material

    PubMed Central

    Westerman, B; Stringfellow, P; Eccleston, J

    2002-01-01

    Objective: To investigate the impact characteristics of an ethylene vinyl acetate (EVA) mouthguard material with regulated air inclusions, which included various air cell volumes and wall thickness between air cells. In particular, the aim was to identify the magnitude and direction of forces within the impacts. Method: EVA mouthguard material, 4 mm thick and with and without air inclusions, was impacted with a constant force impact pendulum with an energy of 4.4 J and a velocity of 3 m/s. Transmitted forces through the EVA material were measured using an accelerometer, which also allowed the determination of force direction and magnitude within the impacts. Results: Statistically significant reductions in the transmitted forces were observed with all the air inclusion materials when compared with EVA without air inclusions. Maximum transmitted force through one air inclusion material was reduced by 32%. Force rebound was eliminated in one material, and reduced second force impulses were observed in all the air inclusion materials. Conclusion: The regulated air inclusions improved the impact characteristics of the EVA mouthguard material, the material most commonly used in mouthguards world wide. PMID:11867493

  18. An effect of the electrode material on space charge relaxation in ferroelectric copolymers of vinylidene fluoride

    SciTech Connect

    Kochervinskii, Valentin Pavlov, Alexey; Pakuro, Natalia; Bessonova, Natalia; Shmakova, Nina; Malyshkina, Inna; Bedin, Sergey

    2015-12-28

    Processes of relaxation of space charges formed by impurities carriers in isotropic films of vinylidene fluoride and tetrafluoroethylene copolymers of the composition 71/29 and 94/6 were studied. Al and Au symmetric electrodes deposited by evaporation in vacuum have been used. In the case of Al electrodes at temperatures above 100 °C, giant low frequency dielectric dispersion was observed, while it is absent in films with Au electrodes. Causes of this phenomenon were studied by the X-ray photoelectron spectroscopy. It was shown that at Al deposition, new functional groups, such as Al-C, Al-F, and Al{sub 2}O{sub 3}, which are not characteristic of the copolymer film surface, formed. They were supposed to be traps for impurity carriers and because of this the electrode became partially blocked. This led to appearance of the giant electrode polarization on the metal-polymer boundary, which did not take place in the case of Au electrodes. Parameters of the Au4f line for the copolymer with different contents of fluorine atoms in the chain were analyzed. An increase in the number of these atoms was shown to result in the line shift to higher energies. This phenomenon was associated with an increase in the shift of the electron density from Au atoms to the F ones which has a high affinity to electrons.

  19. Graphene coated with controllable N-doped carbon layer by molecular layer deposition as electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Chen, Yao; Gao, Zhe; Zhang, Bin; Zhao, Shichao; Qin, Yong

    2016-05-01

    In this work, graphene is coated with nitrogen-doped carbon layer, which is produced by a carbonization process of aromatic polyimide (PI) films deposited on the surfaces of graphene by molecular layer deposition (MLD). The utilization of MLD not only allows uniform coating of PI layers on the surfaces of pristine graphene without any surface treatment, but also enables homogenous dispersion of doped nitrogen atoms in the carbonized products. The as-prepared N-doped carbon layer coated graphene (NC-G) exhibited remarkable capacitance performance as electrode materials for supercapacitor, showing a high specific capacitance of 290.2 F g-1 at current density of 1 A g-1 in 6 M KOH aqueous electrolyte, meanwhile maintaining good rate performance and stable cycle capability. The NC-G synthesized by this way represents an alternative promising candidate as electrode material for supercapacitors.

  20. Hierarchically ordered mesoporous carbon/graphene composites as supercapacitor electrode materials.

    PubMed

    Song, Yanjie; Li, Zhu; Guo, Kunkun; Shao, Ting

    2016-08-25

    Hierarchically ordered mesoporous carbon/graphene (OMC/G) composites have been fabricated by means of a solvent-evaporation-induced self-assembly (EISA) method. The structures of these composites are characterized by X-ray diffraction, transmission electron microscopy, Raman spectroscopy and nitrogen adsorption-desorption at 77 K. These results indicate that OMC/G composites possess the hierarchically ordered hexagonal p6mm mesostructure with the lattice unit parameter and pore diameter close to 10 nm and 3 nm, respectively. The specific surface area of OMC/G composites after KOH activation is high up to 2109.2 m(2) g(-1), which is significantly greater than OMC after activation (1474.6 m(2) g(-1)). Subsequently, the resulting OMC/G composites as supercapacitor electrode materials exhibit an outstanding capacitance as high as 329.5 F g(-1) in 6 M KOH electrolyte at a current density of 0.5 A g(-1), which is much higher than both OMC (234.2 F g(-1)) and a sample made by mechanical mixing of OMC with graphene (217.7 F g(-1)). In addition, the obtained OMC/G composites display good cyclic stability, and the final capacitance retention is approximately 96% after 5000 cycles. These ordered mesopores in the OMC/G composites are beneficial to the accessibility and rapid diffusion of the electrolyte, while graphene in OMC/G composites can also facilitate the transport of electrons during the processes of charging and discharging owing to its high conductivity, thereby leading to an excellent energy storage performance. The method demonstrated in this work would open up a new route to design and develop graphene-based architectures for supercapacitor applications. PMID:27523568

  1. Hierarchically ordered mesoporous carbon/graphene composites as supercapacitor electrode materials.

    PubMed

    Song, Yanjie; Li, Zhu; Guo, Kunkun; Shao, Ting

    2016-08-25

    Hierarchically ordered mesoporous carbon/graphene (OMC/G) composites have been fabricated by means of a solvent-evaporation-induced self-assembly (EISA) method. The structures of these composites are characterized by X-ray diffraction, transmission electron microscopy, Raman spectroscopy and nitrogen adsorption-desorption at 77 K. These results indicate that OMC/G composites possess the hierarchically ordered hexagonal p6mm mesostructure with the lattice unit parameter and pore diameter close to 10 nm and 3 nm, respectively. The specific surface area of OMC/G composites after KOH activation is high up to 2109.2 m(2) g(-1), which is significantly greater than OMC after activation (1474.6 m(2) g(-1)). Subsequently, the resulting OMC/G composites as supercapacitor electrode materials exhibit an outstanding capacitance as high as 329.5 F g(-1) in 6 M KOH electrolyte at a current density of 0.5 A g(-1), which is much higher than both OMC (234.2 F g(-1)) and a sample made by mechanical mixing of OMC with graphene (217.7 F g(-1)). In addition, the obtained OMC/G composites display good cyclic stability, and the final capacitance retention is approximately 96% after 5000 cycles. These ordered mesopores in the OMC/G composites are beneficial to the accessibility and rapid diffusion of the electrolyte, while graphene in OMC/G composites can also facilitate the transport of electrons during the processes of charging and discharging owing to its high conductivity, thereby leading to an excellent energy storage performance. The method demonstrated in this work would open up a new route to design and develop graphene-based architectures for supercapacitor applications.

  2. Layer by Layer Ex-Situ Deposited Cobalt-Manganese Oxide as Composite Electrode Material for Electrochemical Capacitor

    PubMed Central

    Rusi; Chan, P. Y.; Majid, S. R.

    2015-01-01

    The composite metal oxide electrode films were fabricated using ex situ electrodeposition method with further heating treatment at 300°C. The obtained composite metal oxide film had a spherical structure with mass loading from 0.13 to 0.21 mg cm-2. The structure and elements of the composite was investigated using X-ray diffraction (XRD) and energy dispersive X-ray (EDX). The electrochemical performance of different composite metal oxides was studied by cyclic voltammetry (CV) and galvanostatic charge-discharge (CD). As an active electrode material for a supercapacitor, the Co-Mn composite electrode exhibits a specific capacitance of 285 Fg-1 at current density of 1.85 Ag-1 in 0.5M Na2SO4 electrolyte. The best composite electrode, Co-Mn electrode was then further studied in various electrolytes (i.e., 0.5M KOH and 0.5M KOH/0.04M K3Fe(CN) 6 electrolytes). The pseudocapacitive nature of the material of Co-Mn lead to a high specific capacitance of 2.2 x 103 Fg-1 and an energy density of 309 Whkg-1 in a 0.5MKOH/0.04MK3Fe(CN) 6 electrolyte at a current density of 10 Ag-1. The specific capacitance retention obtained 67% of its initial value after 750 cycles. The results indicate that the ex situ deposited composite metal oxide nanoparticles have promising potential in future practical applications. PMID:26158447

  3. Wurtzite copper-zinc-tin sulfide as a superior counter electrode material for dye-sensitized solar cells

    PubMed Central

    2013-01-01

    Wurtzite and kesterite Cu2ZnSnS4 (CZTS) nanocrystals were employed as counter electrode (CE) materials for dye-sensitized solar cells (DSSCs). Compared to kesterite CZTS, the wurtzite CZTS exhibited higher electrocatalytic activity for catalyzing reduction of iodide electrolyte and better conductivity. Accordingly, the DSSC with wurtzite CZTS CE generated higher power conversion efficiency (6.89%) than that of Pt (6.23%) and kesterite CZTS (4.89%) CEs. PMID:24191954

  4. Wurtzite copper-zinc-tin sulfide as a superior counter electrode material for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Kong, Jun; Zhou, Zheng-Ji; Li, Mei; Zhou, Wen-Hui; Yuan, Sheng-Jie; Yao, Rong-Yue; Zhao, Yang; Wu, Si-Xin

    2013-11-01

    Wurtzite and kesterite Cu2ZnSnS4 (CZTS) nanocrystals were employed as counter electrode (CE) materials for dye-sensitized solar cells (DSSCs). Compared to kesterite CZTS, the wurtzite CZTS exhibited higher electrocatalytic activity for catalyzing reduction of iodide electrolyte and better conductivity. Accordingly, the DSSC with wurtzite CZTS CE generated higher power conversion efficiency (6.89%) than that of Pt (6.23%) and kesterite CZTS (4.89%) CEs.

  5. Metallized graphite as an improved cathode material for aluminium/air batteries

    NASA Astrophysics Data System (ADS)

    Mukherjee, Ambick; N. Basumallick, Indra

    1993-06-01

    This paper reports the fabrication of metallized (Pt, Ni, Cu, Fe, Co) graphite cathodes by an electrodeposition method from an appropriate electrolytic bath, together with the performance characteristics of specially-designed aluminium/air cells that utilize these cathodes. In these cells, the aluminium electrodes were separated by a glass-jacket separator. The latter prevents mixing of hydrogen gas evolved due to the corrosion of the aluminium electrode. While the open-circuit voltage of the cells is virtually invariant, the short-circuit current and discharge behaviour are markedly dependent upon the choice of catalytic metal. The discharge profiles are improved markedly for cells with a Pt-, Ni- or Cu-coated graphite air cathode, but the reverse is found for Fe- and Co-coated cathodes. The behaviour is explained in terms of chemisorption and the better catalytic activity of Pt, Ni and Cu. These results suggest that Ni- and Cu-coated graphite air cathodes are promising low-cost and efficiennt electrodes for aluminium/air batteries.

  6. Preparation and photoelectrocatalytic performance of N-doped TiO2/NaY zeolite membrane composite electrode material.

    PubMed

    Cheng, Zhi-Lin; Han, Shuai

    2016-01-01

    A novel composite electrode material based on a N-doped TiO2-loaded NaY zeolite membrane (N-doped TiO2/NaY zeolite membrane) for photoelectrocatalysis was presented. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) and X-ray photoelectron spectroscopy (XPS) characterization techniques were used to analyze the structure of the N-doped TiO2/NaY zeolite membrane. The XRD and SEM results verified that the N-doped TiO2 nanoparticles with the size of ca. 20 nm have been successfully loaded on the porous stainless steel-supported NaY zeolite membrane. The UV-vis result showed that the N-doped TiO2/NaY zeolite membrane exhibited a more obvious red-shift than that of N-TiO2 nanoparticles. The XPS characterization revealed that the doping of N element into TiO2 was successfully achieved. The photoelectrocatalysis performance of the N-doped TiO2/NaY zeolite membrane composite electrode material was evaluated by phenol removal and also the effects of reaction conditions on the catalytic performance were investigated. Owing to exhibiting an excellent catalytic activity and good recycling stability, the N-doped TiO2/NaY zeolite membrane composite electrode material was of promising application for photoelectrocatalysis in wastewater treatment. PMID:26877029

  7. Transition-Metal Carbodiimides as Molecular Negative Electrode Materials for Lithium- and Sodium-Ion Batteries with Excellent Cycling Properties.

    PubMed

    Sougrati, Moulay T; Darwiche, Ali; Liu, Xiaohiu; Mahmoud, Abdelfattah; Hermann, Raphael P; Jouen, Samuel; Monconduit, Laure; Dronskowski, Richard; Stievano, Lorenzo

    2016-04-11

    We report evidence for the electrochemical activity of transition-metal carbodiimides versus lithium and sodium. In particular, iron carbodiimide, FeNCN, can be efficiently used as negative electrode material for alkali-metal-ion batteries, similar to its oxide analogue FeO. Based on (57)Fe Mössbauer and infrared spectroscopy (IR) data, the electrochemical reaction mechanism can be explained by the reversible transformation of the Fe-NCN into Li/Na-NCN bonds during discharge and charge. These new electrode materials exhibit higher capacity compared to well-established negative electrode references such as graphite or hard carbon. Contrary to its oxide analogue, iron carbodiimide does not require heavy treatments (such as nanoscale tailoring, sophisticated textures, or coating) to obtain long cycle life with current density as high as 9 A g(-1) for hundreds of charge-discharge cycles. Similar to the iron compound, several other transition-metal carbodiimides M(x)(NCN)y with M=Mn, Cr, Zn can cycle successfully versus lithium and sodium. Their electrochemical activity and performance open the way to the design of a novel family of anode materials.

  8. Transition-Metal Carbodiimides as Molecular Negative Electrode Materials for Lithium- and Sodium-Ion Batteries with Excellent Cycling Properties

    DOE PAGES

    Sougrati, Moulay T.; Darwiche, Ali; Liu, Xiaohiu; Mahmoud, Abdelfattah; Hermann, Raphael P.; Jouen, Samuel; Monconduit, Laure; Dronskowski, Richard; Stievano, Lorenzo

    2016-03-16

    Here we report evidence for the electrochemical activity of transition-metal carbodiimides versus lithium and sodium. In particular, iron carbodiimide, FeNCN, can be efficiently used as a negative electrode material for alkali-metal-ion batteries, similar to its oxide analogue FeO. Based on 57Fe M ssbauer and infrared spectroscopy (IR) data, the electrochemical reaction mechanism can be explained by the reversible transformation of the Fe NCN into Li/Na NCN bonds during discharge and charge. These new electrode materials exhibit higher capacity compared to well-established negative electrode references such as graphite or hard carbon. Contrary to its oxide analogue, iron carbodiimide does not requiremore » heavy treatments (nanoscale tailoring, sophisticated textures, coating etc.) to obtain long cycle life with density current as high as 9 A/g-1 for hundreds of charge/discharge cycles. Similar to the iron compound, several other transition-metal carbodiimides Mx(NCN)y with M = Mn, Cr, Zn can cycle successfully versus lithium and sodium. Ultimately, their electrochemical activity and performances open the way to the design of a novel family of anode materials.« less

  9. Preparation and photoelectrocatalytic performance of N-doped TiO2/NaY zeolite membrane composite electrode material.

    PubMed

    Cheng, Zhi-Lin; Han, Shuai

    2016-01-01

    A novel composite electrode material based on a N-doped TiO2-loaded NaY zeolite membrane (N-doped TiO2/NaY zeolite membrane) for photoelectrocatalysis was presented. X-ray diffraction (XRD), scanning electron microscopy (SEM), UV-visible (UV-vis) and X-ray photoelectron spectroscopy (XPS) characterization techniques were used to analyze the structure of the N-doped TiO2/NaY zeolite membrane. The XRD and SEM results verified that the N-doped TiO2 nanoparticles with the size of ca. 20 nm have been successfully loaded on the porous stainless steel-supported NaY zeolite membrane. The UV-vis result showed that the N-doped TiO2/NaY zeolite membrane exhibited a more obvious red-shift than that of N-TiO2 nanoparticles. The XPS characterization revealed that the doping of N element into TiO2 was successfully achieved. The photoelectrocatalysis performance of the N-doped TiO2/NaY zeolite membrane composite electrode material was evaluated by phenol removal and also the effects of reaction conditions on the catalytic performance were investigated. Owing to exhibiting an excellent catalytic activity and good recycling stability, the N-doped TiO2/NaY zeolite membrane composite electrode material was of promising application for photoelectrocatalysis in wastewater treatment.

  10. Improved electrochemical performance of boron-doped SiO negative electrode materials in lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Woo, Jihoon; Baek, Seong-Ho; Park, Jung-Soo; Jeong, Young-Min; Kim, Jae Hyun

    2015-12-01

    We introduce a one-step process that consists of thermal disproportionation and impurity doping to enhance the reversible capacity and electrical conductivity of silicon monoxide (SiO)-based negative electrode materials in Li-ion batteries. Transmission electron microscope (TEM) results reveal that thermally treated SiO at 900 °C (H-SiO) consists of uniformly dispersed nano-crystalline Si (nc-Si) in an amorphous silicon oxide (SiOx) matrix. Compared to that of prinstine SiO, the electrochemical performance of H-SiO shows improved specific capacity, due mainly to the increased reversible capacity by nc-Si and to the reduced volume expansion by thermally disproportionated SiOx matrix. Further electrochemical improvements can be obtained by boron-doping on SiO (HB-SiO) using solution dopant during thermal disproportionation. HB-SiO electrode without carbon coating exhibits significantly enhanced specific capacity superior to that of undoped H-SiO electrode, having 947 mAh g-1 at 0.5C rate and excellent capacity retention of 93.3% over 100 cycles. Electrochemical impedance spectroscopy (EIS) measurement reveals that the internal resistance of the HB-SiO electrode is significantly reduced by boron doping.

  11. Scrubbing of contaminants from contaminated air streams with aerogel materials with optional photocatalytic destruction

    DOEpatents

    Attia, Yosry A.

    2000-01-01

    Disclosed is a method for separating a vaporous or gaseous contaminant from an air stream contaminated therewith. This method includes the steps of: (a) passing said contaminated air into a contact zone in which is disposed an aerogel material capable of selecting adsorbing said contaminant from air and therein contacting said contaminated air with an aerogel material; and (b) withdrawing from said zone, air depleted of said contaminant. For present purposes, "contaminant" means a material not naturally occurring in ambient air and/or a material naturally occurring in air but present at a concentration above that found in ambient air. Thus, the present invention scrubs (or treats) air for the purpose of returning it to its ambient composition. Also disclosed herein is a process for the photocatalytic destruction of contaminants from an air stream wherein the contaminated air stream is passed into a control cell or contact zone in which is disposed a photocatalytic aerogel and exposing said aerogel to ultraviolet (UV) radiation for photocatalytically destroying the adsorbed contaminant, and withdrawing from said cell an exhaust air stream depleted in said contaminant.

  12. 49 CFR 175.25 - Notification at air passenger facilities of hazardous materials restrictions.

    Code of Federal Regulations, 2014 CFR

    2014-10-01

    ... 49 Transportation 2 2014-10-01 2014-10-01 false Notification at air passenger facilities of... MATERIALS REGULATIONS CARRIAGE BY AIRCRAFT General Information and Regulations § 175.25 Notification at air... engages in for-hire air transportation of passengers must display notices of the requirements...

  13. A perovskite oxide with high conductivities in both air and reducing atmosphere for use as electrode for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Lan, Rong; Cowin, Peter I.; Sengodan, Sivaprakash; Tao, Shanwen

    2016-08-01

    Electrode materials which exhibit high conductivities in both oxidising and reducing atmospheres are in high demand for solid oxide fuel cells (SOFCs) and solid oxide electrolytic cells (SOECs). In this paper, we investigated Cu-doped SrFe0.9Nb0.1O3‑δ finding that the primitive perovskite oxide SrFe0.8Cu0.1Nb0.1O3‑δ (SFCN) exhibits a conductivity of 63 Scm‑1and 60 Scm‑1 at 415 °C in air and 5%H2/Ar respectively. It is believed that the high conductivity in 5%H2/Ar is related to the exsolved Fe (or FeCu alloy) on exposure to a reducing atmosphere. To the best of our knowledge, the conductivity of SrFe0.8Cu0.1Nb0.1O3‑δ in a reducing atmosphere is the highest of all reported oxides which also exhibit a high conductivity in air. Fuel cell performance using SrFe0.8Cu0.1Nb0.1O3‑δ as the anode, (Y2O3)0.08(ZrO2)0.92 as the electrolyte and La0.8Sr0.2FeO3‑δ as the cathode achieved a power density of 423 mWcm‑2 at 700 °C indicating that SFCN is a promising anode for SOFCs.

  14. A perovskite oxide with high conductivities in both air and reducing atmosphere for use as electrode for solid oxide fuel cells.

    PubMed

    Lan, Rong; Cowin, Peter I; Sengodan, Sivaprakash; Tao, Shanwen

    2016-08-22

    Electrode materials which exhibit high conductivities in both oxidising and reducing atmospheres are in high demand for solid oxide fuel cells (SOFCs) and solid oxide electrolytic cells (SOECs). In this paper, we investigated Cu-doped SrFe0.9Nb0.1O3-δ finding that the primitive perovskite oxide SrFe0.8Cu0.1Nb0.1O3-δ (SFCN) exhibits a conductivity of 63 Scm(-1)and 60 Scm(-1) at 415 °C in air and 5%H2/Ar respectively. It is believed that the high conductivity in 5%H2/Ar is related to the exsolved Fe (or FeCu alloy) on exposure to a reducing atmosphere. To the best of our knowledge, the conductivity of SrFe0.8Cu0.1Nb0.1O3-δ in a reducing atmosphere is the highest of all reported oxides which also exhibit a high conductivity in air. Fuel cell performance using SrFe0.8Cu0.1Nb0.1O3-δ as the anode, (Y2O3)0.08(ZrO2)0.92 as the electrolyte and La0.8Sr0.2FeO3-δ as the cathode achieved a power density of 423 mWcm(-2) at 700 °C indicating that SFCN is a promising anode for SOFCs.

  15. A perovskite oxide with high conductivities in both air and reducing atmosphere for use as electrode for solid oxide fuel cells

    PubMed Central

    Lan, Rong; Cowin, Peter I.; Sengodan, Sivaprakash; Tao, Shanwen

    2016-01-01

    Electrode materials which exhibit high conductivities in both oxidising and reducing atmospheres are in high demand for solid oxide fuel cells (SOFCs) and solid oxide electrolytic cells (SOECs). In this paper, we investigated Cu-doped SrFe0.9Nb0.1O3−δ finding that the primitive perovskite oxide SrFe0.8Cu0.1Nb0.1O3−δ (SFCN) exhibits a conductivity of 63 Scm−1and 60 Scm−1 at 415 °C in air and 5%H2/Ar respectively. It is believed that the high conductivity in 5%H2/Ar is related to the exsolved Fe (or FeCu alloy) on exposure to a reducing atmosphere. To the best of our knowledge, the conductivity of SrFe0.8Cu0.1Nb0.1O3−δ in a reducing atmosphere is the highest of all reported oxides which also exhibit a high conductivity in air. Fuel cell performance using SrFe0.8Cu0.1Nb0.1O3−δ as the anode, (Y2O3)0.08(ZrO2)0.92 as the electrolyte and La0.8Sr0.2FeO3−δ as the cathode achieved a power density of 423 mWcm−2 at 700 °C indicating that SFCN is a promising anode for SOFCs. PMID:27545200

  16. Interesting electrochemical properties of novel three-dimensional Ag3PO4 tetrapods as a new super capacitor electrode material

    NASA Astrophysics Data System (ADS)

    Li, Shouguang; Teng, Fei; Chen, Mindong; Li, Na; Hua, Xia; Wang, Kai; Li, Min

    2014-05-01

    The novel three-dimensional (3D) silver phosphate tetrapods (TA) are synthesized and employed as a super capacitor electrode material. The electrochemical properties are investigated by cyclic voltammetry (CV), chronopotentiometry (CP) and electrochemical impedance spectroscopy (EIS). It is interesting that compared with irregular silver phosphate particles (IA), TA shows a higher capacitance (250 vs. 160 F g-1), and a higher coulombic efficiency (80% vs. 74%), which is mainly ascribed to the 3D microstructure and its high conductivity. To the best of our knowledge, this is the first report on silver phosphate as a super capacitor material.

  17. 49 CFR 175.25 - Notification at air passenger facilities of hazardous materials restrictions.

    Code of Federal Regulations, 2011 CFR

    2011-10-01

    ... 49 Transportation 2 2011-10-01 2011-10-01 false Notification at air passenger facilities of... MATERIALS REGULATIONS CARRIAGE BY AIRCRAFT General Information and Regulations § 175.25 Notification at air passenger facilities of hazardous materials restrictions. (a) Each person who engages in for-hire...

  18. 49 CFR 175.25 - Notification at air passenger facilities of hazardous materials restrictions.

    Code of Federal Regulations, 2012 CFR

    2012-10-01

    ... 49 Transportation 2 2012-10-01 2012-10-01 false Notification at air passenger facilities of... MATERIALS REGULATIONS CARRIAGE BY AIRCRAFT General Information and Regulations § 175.25 Notification at air passenger facilities of hazardous materials restrictions. (a) Each person who engages in for-hire...

  19. The effect of electrode material on the motion of a plasma piston in rail accelerators

    NASA Astrophysics Data System (ADS)

    Bobashev, S. V.; Zhukov, B. G.; Kurakin, R. O.; Ponyaev, S. A.; Reznikov, B. I.

    2015-10-01

    The acceleration of a plasma piston in the channels of rail accelerators with copper and graphite electrodes is studied experimentally. It is found that the plasma velocity is reduced by 15-20% (at equal discharge currents) when graphite electrodes are used instead of copper ones. This may be attributed to an increase in the erosion graphite mass that is drawn into motion by the plasma piston. It is concluded based on the interpretation of the obtained data that the current flow in the channels of rail accelerators is governed at high plasma speeds by the processes of thermoautoelectron emission.

  20. Avoiding Errors in Electrochemical Measurements: Effect of Frit Material on the Performance of Reference Electrodes with Porous Frit Junctions.

    PubMed

    Mousavi, Maral P S; Saba, Stacey A; Anderson, Evan L; Hillmyer, Marc A; Bühlmann, Philippe

    2016-09-01

    In many commercially available and in-house-prepared reference electrodes, nanoporous glass frits (often of the brand named Vycor) contain the electrolyte solution that forms a salt bridge between the sample and the reference solution. Recently, we showed that in samples with low ionic strength, the half-cell potentials of reference electrodes comprising nanoporous Vycor frits are affected by the sample and can shift in response to the sample composition by more than 50 mV (which can cause up to 900% error in potentiometric measurements). It was confirmed that the large potential variations result from electrostatic screening of ion transfer through the frit due to the negatively charged surfaces of the glass nanopores. Since the commercial production of porous Vycor glass was recently discontinued, new materials have been used lately as porous frits in commercially available reference electrodes, namely frits made of Teflon, polyethylene, or one of two porous glasses sold under the brand names CoralPor and Electro-porous KT. In this work, we studied the effect of the frit characteristics on the performance of reference electrodes, and show that the unwanted changes in the reference potential are not unique to electrodes with Vycor frits. Increasing the pore size in the glass frits from the <10 nm into the 1 μm range or switching to polymeric frits with pores in the 1 to 10 μm range nearly eliminates the potential variations caused by electrostatic screening of ion transport through the frit pores. Unfortunately, bigger frit pores result in larger flow rates of the reference solution through the pores, which can result in the contamination of test solutions. PMID:27464837

  1. Fabrication of a flexible and conductive lyocell fabric decorated with graphene nanosheets as a stable electrode material.

    PubMed

    Mengal, Naveed; Sahito, Iftikhar Ali; Arbab, Alvira Ayoub; Sun, Kyung Chul; Qadir, Muhammad Bilal; Memon, Anam Ali; Jeong, Sung Hoon

    2016-11-01

    Textile electrodes are highly desirable for wearable electronics as they offer light-weight, flexibility, cost effectiveness and ease of fabrication. Here, we propose the use of lyocell fabric as a flexible textile electrode because of its inherently super hydrophilic characteristics and increased moisture uptake. A highly concentrated colloidal solution of graphene oxide nanosheets (GONs) was coated on to lyocell fabric and was then reduced in to graphene nanosheets (GNs) using facile chemical reduction method. The proposed textile electrode has a very high surface conductivity with a very low value of surface resistance of only 40Ωsq(-1), importantly without use of any binding or adhesive material in the processing step. Atomic force spectroscopy (AFM) and Transmission electron microscopy (TEM) were conducted to study the topographical properties and sheet exfoliation of prepared GONs. The surface morphology, structural characterization and thermal stability of the fabricated textile electrode were studied by field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), X ray photon spectroscopy (XPS), Raman spectroscopy, Wide angle X ray diffraction spectroscopy (WAXD) and Thermogravimetric analysis (TGA) respectively. These results suggest that the GONs is effectively adhered on to the lyocell fabric and the conversion of GONs in to GNs by chemical reduction has no adverse effect on the crystalline structure of textile substrate. The prepared graphene coated conductive lyocell fabric was found stable in water and electrolyte solution and it maintained nearly same surface electrical conductivity at various bending angles. The electrical resistance results suggest that this lyocell based textile electrode (L-GNs) is a promising candidate for flexible and wearable electronics and energy harvesting devices. PMID:27516245

  2. Avoiding Errors in Electrochemical Measurements: Effect of Frit Material on the Performance of Reference Electrodes with Porous Frit Junctions.

    PubMed

    Mousavi, Maral P S; Saba, Stacey A; Anderson, Evan L; Hillmyer, Marc A; Bühlmann, Philippe

    2016-09-01

    In many commercially available and in-house-prepared reference electrodes, nanoporous glass frits (often of the brand named Vycor) contain the electrolyte solution that forms a salt bridge between the sample and the reference solution. Recently, we showed that in samples with low ionic strength, the half-cell potentials of reference electrodes comprising nanoporous Vycor frits are affected by the sample and can shift in response to the sample composition by more than 50 mV (which can cause up to 900% error in potentiometric measurements). It was confirmed that the large potential variations result from electrostatic screening of ion transfer through the frit due to the negatively charged surfaces of the glass nanopores. Since the commercial production of porous Vycor glass was recently discontinued, new materials have been used lately as porous frits in commercially available reference electrodes, namely frits made of Teflon, polyethylene, or one of two porous glasses sold under the brand names CoralPor and Electro-porous KT. In this work, we studied the effect of the frit characteristics on the performance of reference electrodes, and show that the unwanted changes in the reference potential are not unique to electrodes with Vycor frits. Increasing the pore size in the glass frits from the <10 nm into the 1 μm range or switching to polymeric frits with pores in the 1 to 10 μm range nearly eliminates the potential variations caused by electrostatic screening of ion transport through the frit pores. Unfortunately, bigger frit pores result in larger flow rates of the reference solution through the pores, which can result in the contamination of test solutions.

  3. Fabrication of a flexible and conductive lyocell fabric decorated with graphene nanosheets as a stable electrode material.

    PubMed

    Mengal, Naveed; Sahito, Iftikhar Ali; Arbab, Alvira Ayoub; Sun, Kyung Chul; Qadir, Muhammad Bilal; Memon, Anam Ali; Jeong, Sung Hoon

    2016-11-01

    Textile electrodes are highly desirable for wearable electronics as they offer light-weight, flexibility, cost effectiveness and ease of fabrication. Here, we propose the use of lyocell fabric as a flexible textile electrode because of its inherently super hydrophilic characteristics and increased moisture uptake. A highly concentrated colloidal solution of graphene oxide nanosheets (GONs) was coated on to lyocell fabric and was then reduced in to graphene nanosheets (GNs) using facile chemical reduction method. The proposed textile electrode has a very high surface conductivity with a very low value of surface resistance of only 40Ωsq(-1), importantly without use of any binding or adhesive material in the processing step. Atomic force spectroscopy (AFM) and Transmission electron microscopy (TEM) were conducted to study the topographical properties and sheet exfoliation of prepared GONs. The surface morphology, structural characterization and thermal stability of the fabricated textile electrode were studied by field emission scanning electron microscopy (FE-SEM), Fourier transform infrared spectroscopy (FT-IR), X ray photon spectroscopy (XPS), Raman spectroscopy, Wide angle X ray diffraction spectroscopy (WAXD) and Thermogravimetric analysis (TGA) respectively. These results suggest that the GONs is effectively adhered on to the lyocell fabric and the conversion of GONs in to GNs by chemical reduction has no adverse effect on the crystalline structure of textile substrate. The prepared graphene coated conductive lyocell fabric was found stable in water and electrolyte solution and it maintained nearly same surface electrical conductivity at various bending angles. The electrical resistance results suggest that this lyocell based textile electrode (L-GNs) is a promising candidate for flexible and wearable electronics and energy harvesting devices.

  4. Air emissions from exposed contaminated sediments and dredged material

    SciTech Connect

    Valsaraj, K.T.; Ravikrishna, R.; Reible, D.D.; Thibodeaux, L.J.; Choy, B.; Price, C.B.; Brannon, J.M.; Myers, T.E.; Yost, S.

    1999-01-01

    The sediment-to-air fluxes of two polycyclic aromatic hydrocarbons (phenanthrene and pyrene) and a heterocyclic aromatic hydrocarbon (dibenzofuran) from a laboratory-contaminated sediment and those of three polycyclic aromatic hydrocarbons (naphthalene, phenanthrene, and pyrene) from three field sediments were investigated in experimental microcosms. The flux was dependent on the sediment moisture content, air-filled porosity, and the relative humidity of the air flowing over the sediment surface. The mathematical model predictions of flux from the laboratory-spiked sediment agreed with observed values. The fluxes of compounds with higher hydrophobicity were more air-side resistance controlled. Conspicuous differences were observed between the fluxes from the laboratory-spiked and two of the three field sediments. Two field sediments showed dramatic increases in mass-transfer resistances with increasing exposure time and had significant fractions of oil and grease. The proposed mathematical model was inadequate for predicting the flux from the latter field sediments. Sediment reworking enhanced the fluxes from the field sediments due to exposure of fresh solids to the air. Variations in flux from the lab-spiked sediment as a result of change in air relative humidity were due to differences in retardation of chemicals on a dry or wet surface sediment. High moisture in the air over the dry sediment increased the competition for sorption sites between water and contaminant and increased the contaminant flux.

  5. The preparation and performance of calcium carbide-derived carbon/polyaniline composite electrode material for supercapacitors

    NASA Astrophysics Data System (ADS)

    Zheng, Liping; Wang, Ying; Wang, Xianyou; Li, Na; An, Hongfang; Chen, Huajie; Guo, Jia

    Calcium carbide (CaC 2)-derived carbon (CCDC)/polyaniline (PANI) composite materials are prepared by in situ chemical oxidation polymerization of an aniline solution containing well-dispersed CCDC. The structure and morphology of CCDC/PANI composite are characterized by Fourier infrared spectroscopy (FTIR), scanning electron microscope (SEM), transmission electron microscopy (TEM) and N 2 sorption isotherms. It has been found that PANI was uniformly deposited on the surface and the inner pores of CCDC. The supercapacitive behaviors of the CCDC/PANI composite materials are investigated with cyclic voltammetry (CV), galvanostatic charge/discharge and cycle life measurements. The results show that the CCDC/PANI composite electrodes have higher specific capacitances than the as grown CCDC electrodes and higher stability than the conducting polymers. The capacitance of CCDC/PANI composite electrode is as high as 713.4 F g -1 measured by cyclic voltammetry at 1 mV s -1. Besides, the capacitance retention of coin supercapacitor remained 80.1% after 1000 cycles.

  6. A Graphene Composite Material with Single Cobalt Active Sites: A Highly Efficient Counter Electrode for Dye-Sensitized Solar Cells.

    PubMed

    Cui, Xiaoju; Xiao, Jianping; Wu, Yihui; Du, Peipei; Si, Rui; Yang, Huaixin; Tian, Huanfang; Li, Jianqi; Zhang, Wen-Hua; Deng, Dehui; Bao, Xinhe

    2016-06-01

    The design of catalysts that are both highly active and stable is always challenging. Herein, we report that the incorporation of single metal active sites attached to the nitrogen atoms in the basal plane of graphene leads to composite materials with superior activity and stability when used as counter electrodes in dye-sensitized solar cells (DSSCs). A series of composite materials based on different metals (Mn, Fe, Co, Ni, and Cu) were synthesized and characterized. Electrochemical measurements revealed that CoN4 /GN is a highly active and stable counter electrode for the interconversion of the redox couple I(-) /I3 (-) . DFT calculations revealed that the superior properties of CoN4 /GN are due to the appropriate adsorption energy of iodine on the confined Co sites, leading to a good balance between adsorption and desorption processes. Its superior electrochemical performance was further confirmed by fabricating DSSCs with CoN4  /GN electrodes, which displayed a better power conversion efficiency than the Pt counterpart. PMID:27089044

  7. A Graphene Composite Material with Single Cobalt Active Sites: A Highly Efficient Counter Electrode for Dye-Sensitized Solar Cells.

    PubMed

    Cui, Xiaoju; Xiao, Jianping; Wu, Yihui; Du, Peipei; Si, Rui; Yang, Huaixin; Tian, Huanfang; Li, Jianqi; Zhang, Wen-Hua; Deng, Dehui; Bao, Xinhe

    2016-06-01

    The design of catalysts that are both highly active and stable is always challenging. Herein, we report that the incorporation of single metal active sites attached to the nitrogen atoms in the basal plane of graphene leads to composite materials with superior activity and stability when used as counter electrodes in dye-sensitized solar cells (DSSCs). A series of composite materials based on different metals (Mn, Fe, Co, Ni, and Cu) were synthesized and characterized. Electrochemical measurements revealed that CoN4 /GN is a highly active and stable counter electrode for the interconversion of the redox couple I(-) /I3 (-) . DFT calculations revealed that the superior properties of CoN4 /GN are due to the appropriate adsorption energy of iodine on the confined Co sites, leading to a good balance between adsorption and desorption processes. Its superior electrochemical performance was further confirmed by fabricating DSSCs with CoN4  /GN electrodes, which displayed a better power conversion efficiency than the Pt counterpart.

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

    SciTech Connect

    Visco, Steven J

    2015-11-30

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

  9. Study of electrochemical properties of thin film materials obtained using plasma technologies for production of electrodes for pacemakers

    NASA Astrophysics Data System (ADS)

    Obrezkov, O. I.; Vinogradov, V. P.; Krauz, V. I.; Mozgrin, D. V.; Guseva, I. A.; Andreev, E. S.; Zverev, A. A.; Starostin, A. L.

    2016-09-01

    Studies of thin film materials (TFM) as coatings of tips of pacemaker electrodes implanted into the human heart have been performed. TFM coatings were deposited in vacuum by arc magnetron discharge plasma, by pulsed discharge of “Plasma Focus”, and by electron beam evaporation. Simulation of electric charge transfer to the heart in physiological blood- imitator solution and determination of electrochemical properties of the coatings were carried out. TFM of highly developed surface of contact with tissue was produced by argon plasma spraying of titanium powder with subsequent coating by titanium nitride in vacuum arc assisted by Ti ion implantation. The TFM coatings of pacemaker electrode have passed necessary clinical tests and were used in medical practice. They provide low voltage myocardium stimulation thresholds within the required operating time.

  10. Electrochemical investigation of functionalized graphene aerogel with different amount of p-phenylenediamine as an advanced electrode material for supercapacitors

    NASA Astrophysics Data System (ADS)

    Gholipour-Ranjbar, Habib; Ganjali, Mohammad Reza; Norouzi, Parviz; Naderi, Hamid Reza

    2016-07-01

    Graphene aerogel has attracted great attention as a new and efficient electrode material for supercapacitors. It can be expected that functionalization of graphene aerogels can further improve their capability. In this study, graphene aerogel functionalized with different amount of p-phenylenediamine (PPD) and the effect of PPD amount on the supercapacitive performance of functionalized graphene aerogel (FGA) was investigated. Structural characterizations showed that PPD molecules initiated graphene aerogel sheets assembly into three-dimensional structures and also increasing PPD amount led to increase in surface area. Electrochemical investigations proved that the FGA with larger pore size showed enhanced supercapacitive performance compared with the FGA with smaller pore size. The optimized FGA-based electrode exhibited outstanding specific capacitance (SC) of 385 F g‑1 at a discharge current density of 1 A g‑1, good rate capability (215 F g‑1 at 20 A g‑1), and exceptionally high cyclic stability by displaying 25% increase in SC after 5000 cycle.

  11. Method of preparing a positive electrode for an electrochemical cell

    DOEpatents

    Tomczuk, Zygmunt

    1979-01-01

    A method of preparing an electrochemical cell including a metal sulfide as the positive electrode reactant and lithium alloy as the negative electrochemical reactant with an alkali metal, molten salt electrolyte is disclosed which permits the assembly to be accomplished in air. The electrode reactants are introduced in the most part as a sulfide of lithium and the positive electrode metal in a single-phase compound. For instance, Li.sub.2 FeS.sub.2 is a single-phase compound that is produced by the reaction of Li.sub.2 S and FeS. This compound is an intermediate in the positive electrode cycle from FeS.sub.2 to Fe and Li.sub.2 S. Its use minimizes volumetric changes from the assembled to the charged and discharged conditions of the electrode and minimizes electrode material interaction with air and moisture during assembly.

  12. Layered electrode for electrochemical cells

    DOEpatents

    Swathirajan, Swathy; Mikhail, Youssef M.

    2001-01-01

    There is provided an electrode structure comprising a current collector sheet and first and second layers of electrode material. Together, the layers improve catalyst utilization and water management.

  13. Applying a tapered electrode on a porous ceramic support tube by masking a band inside the tube and drawing in electrode material from the outside of the tube by suction

    DOEpatents

    Vasilow, T.R.; Zymboly, G.E.

    1991-12-17

    An electrode is deposited on a support by providing a porous ceramic support tube having an open end and closed end; masking at least one circumferential interior band inside the tube; evacuating air from the tube by an evacuation system, to provide a permeability gradient between the masked part and unmasked part of the tube; applying a liquid dispersion of solid electrode particles to the outside surface of the support tube, where liquid flows through the wall, forming a uniform coating over the unmasked support part and a tapered coating over the masked part. 2 figures.

  14. Applying a tapered electrode on a porous ceramic support tube by masking a band inside the tube and drawing in electrode material from the outside of the tube by suction

    DOEpatents

    Vasilow, Theodore R.; Zymboly, Gregory E.

    1991-01-01

    An electrode is deposited on a support by providing a porous ceramic support tube (10) having an open end (14) and closed end (16); masking at least one circumferential interior band (18 and 18') inside the tube; evacuating air from the tube by an evacuation system (30), to provide a permeability gradient between the masked part (18 and 18') and unmasked part (20) of the tube; applying a liquid dispersion of solid electrode particles to the outside surface of the support tube, where liquid flows through the wall, forming a uniform coating (42) over the unmasked support part (20) and a tapered coating over the masked part (18 and 18').

  15. Air

    MedlinePlus

    ... do to protect yourself from dirty air . Indoor air pollution and outdoor air pollution Air can be polluted indoors and it can ... this chart to see what things cause indoor air pollution and what things cause outdoor air pollution! Indoor ...

  16. Surface loss probability of atomic hydrogen for different electrode cover materials investigated in H₂-Ar low-pressure plasmas

    SciTech Connect

    Sode, M. Schwarz-Selinger, T.; Jacob, W.; Kersten, H.

    2014-07-07

    In an inductively coupled H₂-Ar plasma at a total pressure of 1.5 Pa, the influence of the electrode cover material on selected line intensities of H, H₂, and Ar are determined by optical emission spectroscopy and actinometry for the electrode cover materials stainless steel, copper, tungsten, Macor{sup ®}, and aluminum. Hydrogen dissociation degrees for the considered conditions are determined experimentally from the measured emission intensity ratios. The surface loss probability β{sub H} of atomic hydrogen is correlated with the measured line intensities, and β{sub H} values are determined for the considered materials. Without the knowledge of the atomic hydrogen temperature, β{sub H} cannot be determined exactly. However, ratios of β{sub H} values for different surface materials are in first order approximation independent of the atomic hydrogen temperature. Our results show that β{sub H} of copper is equal to the value of stainless steel, β{sub H} of Macor{sup ®} and tungsten is about 2 times smaller and β{sub H} of aluminum about 5 times smaller compared with stainless steel. The latter ratio is in reasonable agreement with literature. The influence of the atomic hydrogen temperature T{sub H} on the absolute value is thoroughly discussed. For our assumption of T{sub H}=600 K, we determine a β{sub H} for stainless steel of 0.39±0.13.

  17. IAEA regulatory initiatives for the air transport of large quantities of radioactive materials

    SciTech Connect

    Luna, Robert E.; Wangler, Michael W.; Selling, Hendrik A.

    1992-01-01

    The International Atomic Energy Agency (IAEA) has been laboring since 1988 over a far reaching change to its model regulations (IAEA, 1990) for the transport of radioactive materials (RAM). This change could impact the manner in which certain classes of radioactive materials are shipped by air and change some of the basic tenets of radioactive material transport regulations around the world. This report discusses issues associated with air transport regulations.

  18. Li-Rich Li-Si Alloy As A Lithium-Containing Negative Electrode Material Towards High Energy Lithium-Ion Batteries

    PubMed Central

    Iwamura, Shinichiroh; Nishihara, Hirotomo; Ono, Yoshitaka; Morito, Haruhiko; Yamane, Hisanori; Nara, Hiroki; Osaka, Tetsuya; Kyotani, Takashi

    2015-01-01

    Lithium-ion batteries (LIBs) are generally constructed by lithium-including positive electrode materials, such as LiCoO2, and lithium-free negative electrode materials, such as graphite. Recently, lithium-free positive electrode materials, such as sulfur, are gathering great attention from their very high capacities, thereby significantly increasing the energy density of LIBs. Though the lithium-free materials need to be combined with lithium-containing negative electrode materials, the latter has not been well developed yet. In this work, the feasibility of Li-rich Li-Si alloy is examined as a lithium-containing negative electrode material. Li-rich Li-Si alloy is prepared by the melt-solidification of Li and Si metals with the composition of Li21Si5. By repeating delithiation/lithiation cycles, Li-Si particles turn into porous structure, whereas the original particle size remains unchanged. Since Li-Si is free from severe constriction/expansion upon delithiation/lithiation, it shows much better cyclability than Si. The feasibility of the Li-Si alloy is further examined by constructing a full-cell together with a lithium-free positive electrode. Though Li-Si alloy is too active to be mixed with binder polymers, the coating with carbon-black powder by physical mixing is found to prevent the undesirable reactions of Li-Si alloy with binder polymers, and thus enables the construction of a more practical electrochemical cell. PMID:25626879

  19. Electrochemical sensor for nitroaromatic type energetic materials using gold nanoparticles/poly(o-phenylenediamine-aniline) film modified glassy carbon electrode.

    PubMed

    Sağlam, Şener; Üzer, Ayşem; Tekdemir, Yasemin; Erçağ, Erol; Apak, Reşat

    2015-07-01

    In this work, a novel electrochemical sensor was developed for the detection of nitroaromatic explosive materials, based on a gold nanoparticle-modified glassy carbon (GC) electrode coated with poly(o-phenylenediamine-aniline film) (GC/P(o-PDA-co-ANI)-Aunano electrode). Nitroaromatic compounds were detected through their π-acceptor/donor interactions with o-phenylenediamine-aniline functionalities on the modified electrode surface. The enhanced sensitivities were achieved through π-π and charge-transfer (CT) interactions between the electron-deficient nitroaromatic compounds and σ-/π-donor amine/aniline groups linked to gold nanoparticles (Au-NPs), providing increased binding and preconcentration onto the modified GC-electrodes. Selective determination of nitroaromatic type explosives in the presence of nitramines was enabled by o-PDA and reusability of the electrode achieved by Au-NPs. Calibration curves of current intensity versus concentration were linear in the range of 2.5-40mgL(-1) for 2,4,6-trinitrotoluene (TNT) with a detection limit (LOD) of 2.1mgL(-1), 2-40mgL(-1) for 2,4-dinitrotoluene (DNT) (LOD=1.28mgL(-1)), 5-100mgL(-1) for tetryl (LOD=3.8mgL(-1)) with the use of the GC/P(o-PDA-co-ANI)-Aunano electrode. For sensor measurements, coefficients of variation of intra- and inter-assay measurements were 0.6% and 1.2%, respectively (N=5), confirming the high reproducibility of the proposed assay. Deconvolution of current contributions of synthetic (TNT+DNT) mixtures at peak potentials of constituents was performed by multiple linear regression analysis to provide high sensitivity for the determination of each constituent. Determination options for all possible mixture combinations of nitroaromatic explosives are presented in this work. The proposed methods were successfully applied to the analysis of nitroaromatics in military explosives, namely comp B, octol, and tetrytol. Method validation was performed against GC-MS on real post-blast residual samples

  20. Nitrogen-Doped Porous Carbons As Electrode Materials for High-Performance Supercapacitor and Dye-Sensitized Solar Cell.

    PubMed

    Wang, Lan; Gao, Zhiyong; Chang, Jiuli; Liu, Xiao; Wu, Dapeng; Xu, Fang; Guo, Yuming; Jiang, Kai

    2015-09-16

    Activated N-doped porous carbons (a-NCs) were synthesized by pyrolysis and alkali activation of graphene incorporated melamine formaldehyde resin (MF). The moderate N doping levels, mesopores rich porous texture, and incorporation of graphene enable the applications of a-NCs in surface and conductivity dependent electrode materials for supercapacitor and dye-sensitized solar cell (DSSC). Under optimal activation temperature of 700 °C, the afforded sample, labeled as a-NC700, possesses a specific surface area of 1302 m2 g(-1), a N fraction of 4.5%, and a modest graphitization. When used as a supercapacitor electrode, a-NC700 offers a high specific capacitance of 296 F g(-1) at a current density of 1 A g(-1), an acceptable rate capability, and a high cycling stability in 1 M H2SO4 electrolyte. As a result, a-NC700 supercapacitor delivers energy densities of 5.0-3.5 Wh kg(-1) under power densities of 83-1609 W kg(-1). Moreover, a-NC700 also demonstrates high electrocatalytic activity for I3- reduction. When employed as a counter electrode (CE) of DSSC, a power conversion efficiency (PCE) of 6.9% is achieved, which is comparable to that of the Pt CE based counterpart (7.1%). The excellent capacitive and photovoltaic performances highlight the potential of a-NCs in sustainable energy devices.

  1. Interconnecting Carbon Fibers with the In-situ Electrochemically Exfoliated Graphene as Advanced Binder-free Electrode Materials for Flexible Supercapacitor

    PubMed Central

    Zou, Yuqin; Wang, Shuangyin

    2015-01-01

    Flexible energy storage devices are highly demanded for various applications. Carbon cloth (CC) woven by carbon fibers (CFs) is typically used as electrode or current collector for flexible devices. The low surface area of CC and the presence of big gaps (ca. micro-size) between individual CFs lead to poor performance. Herein, we interconnect individual CFs through the in-situ exfoliated graphene with high surface area by the electrochemical intercalation method. The interconnected CFs are used as both current collector and electrode materials for flexible supercapacitors, in which the in-situ exfoliated graphene act as active materials and conductive “binders”. The in-situ electrochemical intercalation technique ensures the low contact resistance between electrode (graphene) and current collector (carbon cloth) with enhanced conductivity. The as-prepared electrode materials show significantly improved performance for flexible supercapacitors. PMID:26149290

  2. Interconnecting Carbon Fibers with the In-situ Electrochemically Exfoliated Graphene as Advanced Binder-free Electrode Materials for Flexible Supercapacitor.

    PubMed

    Zou, Yuqin; Wang, Shuangyin

    2015-07-07

    Flexible energy storage devices are highly demanded for various applications. Carbon cloth (CC) woven by carbon fibers (CFs) is typically used as electrode or current collector for flexible devices. The low surface area of CC and the presence of big gaps (ca. micro-size) between individual CFs lead to poor performance. Herein, we interconnect individual CFs through the in-situ exfoliated graphene with high surface area by the electrochemical intercalation method. The interconnected CFs are used as both current collector and electrode materials for flexible supercapacitors, in which the in-situ exfoliated graphene act as active materials and conductive "binders". The in-situ electrochemical intercalation technique ensures the low contact resistance between electrode (graphene) and current collector (carbon cloth) with enhanced conductivity. The as-prepared electrode materials show significantly improved performance for flexible supercapacitors.

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

    PubMed

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

    2015-12-01

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

  4. Novel GO-LaSmO2 Nanocomposite as an Effective Electrode Material for Hydrogen Fuel Cells

    NASA Astrophysics Data System (ADS)

    El-Amin, Ayman A.; Othman, Abdelhameed M.

    2016-04-01

    Nano-composites of lanthanum-samarium oxide (LaSmO2) were prepared in the absence and presence of graphene oxide (GO) and characterized as an effective electrode material for hydrogen fuel cells. X-ray and scanning electron microscope investigations revealed grain sizes of 8 nm for LaSmO2 and 12 nm for GO-LaSmO2 composites. The x-ray diffraction pattern showed sharp peaks, indicating a well-crystallized phase indexable to a rhombohedral structure with space group R 3 C , and their structural refinement performed in the hexagonal mode. The ionic conductivity of LaSmO2 was found to be 4.12 × 10-5 S/cm, while in the presence of GO it was enhanced to 5.32 × 10-5 S/cm. The mechanism of conduction in the proposed nano-materials was investigated based on frequency exponent S. The values of S were observed to decrease with increasing temperature. This result was found to be in good agreement with the correlated barrier hopping (CBH) model. The present work revealed GO to be a conductivity enhancer that caused the GO-LaSmO2 composite to be an effective electrode material for hydrogen fuel cells.

  5. Facile construction of 3D graphene/MoS2 composites as advanced electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Sun, Tianhua; Li, Zhangpeng; Liu, Xiaohong; Ma, Limin; Wang, Jinqing; Yang, Shengrong

    2016-11-01

    Flower-like molybdenum disulfide (MoS2) microstructures are synthesized based on three-dimensional graphene (3DG) skeleton via a simple and facile one-step hydrothermal method, aiming at constructing series of novel composite electrode materials of 3DG/MoS2 with high electrochemical performances for supercapacitors. The electrochemical properties of the samples are evaluated by cyclic voltammetry and galvanostatic charge/discharge tests. Specifically, the optimal 3DG/MoS2 composite exhibits remarkable performances with a high specific capacitance of 410 F g-1 at a current density of 1 A g-1 and an excellent cycling stability with ca. 80.3% capacitance retention after 10,000 continuous charge-discharge cycles at a high current density of 2 A g-1, making it adaptive for high-performance supercapacitors. The enhanced electrochemical performances can be ascribed to the combination of 3DG and flower-like MoS2, which provides excellent charge transfer network and electrolyte diffusion channels while effectively prevents the collapse, aggregation and morphology change of active materials during charge-discharge process. The results demonstrate that 3DG/MoS2 composite is one of the attractive electrode materials for supercapacitors.

  6. Effect of electrode material on characteristics of non-volatile resistive memory consisting of Ag2S nanoparticles

    NASA Astrophysics Data System (ADS)

    Jang, Jaewon

    2016-07-01

    In this study, Ag2S nanoparticles are synthesized and used as the active material for two-terminal resistance switching memory devices. Sintered Ag2S films are successfully crystallized on plastic substrates with synthesized Ag2S nanoparticles, after a relatively low-temperature sintering process (200 °C). After the sintering process, the crystallite size is increased from 6.8 nm to 80.3 nm. The high ratio of surface atoms to inner atoms of nanoparticles reduces the melting point temperature, deciding the sintering process temperature. In order to investigate the resistance switching characteristics, metal/Ag2S/metal structures are fabricated and tested. The effect of the electrode material on the non-volatile resistive memory characteristics is studied. The bottom electrochemically inert materials, such as Au and Pt, were critical for maintaining stable memory characteristics. By using Au and Pt inert bottom electrodes, we are able to significantly improve the memory endurance and retention to more than 103 cycles and 104 sec, respectively.

  7. High-energy metal air batteries

    DOEpatents

    Zhang, Ji-Guang; Xiao, Jie; Xu, Wu; Wang, Deyu; Williford, Ralph E.; Liu, Jun

    2013-07-09

    Disclosed herein are embodiments of lithium/air batteries and methods of making and using the same. Certain embodiments are pouch-cell batteries encased within an oxygen-permeable membrane packaging material that is less than 2% of the total battery weight. Some embodiments include a hybrid air electrode comprising carbon and an ion insertion material, wherein the mass ratio of ion insertion material to carbon is 0.2 to 0.8. The air electrode may include hydrophobic, porous fibers. In particular embodiments, the air electrode is soaked with an electrolyte comprising one or more solvents including dimethyl ether, and the dimethyl ether subsequently is evacuated from the soaked electrode. In other embodiments, the electrolyte comprises 10-20% crown ether by weight.

  8. High-energy metal air batteries

    DOEpatents

    Zhang, Ji-Guang; Xiao, Jie; Xu, Wu; Wang, Deyu; Williford, Ralph E.; Liu, Jun

    2014-07-01

    Disclosed herein are embodiments of lithium/air batteries and methods of making and using the same. Certain embodiments are pouch-cell batteries encased within an oxygen-permeable membrane packaging material that is less than 2% of the total battery weight. Some embodiments include a hybrid air electrode comprising carbon and an ion insertion material, wherein the mass ratio of ion insertion material to carbon is 0.2 to 0.8. The air electrode may include hydrophobic, porous fibers. In particular embodiments, the air electrode is soaked with an electrolyte comprising one or more solvents including dimethyl ether, and the dimethyl ether subsequently is evacuated from the soaked electrode. In other embodiments, the electrolyte comprises 10-20% crown ether by weight.

  9. New electrosurgical ball electrode with nonstick properties

    NASA Astrophysics Data System (ADS)

    Rondinone, Joseph; Brassell, James; Miller, Scott A., III; Thorne, Jonathan O.; Rondinone, David M.; Safabash, Jason; Vega, Felix

    1998-04-01

    A new electrosurgical ball electrode (SilverBulletTM) has been developed for applying radiofrequency (RF) energy to fuse biological and other materials to tissue surfaces. Specifically, the electrode was developed for use in conjunction with the Fusion Medical Technologies, Inc. gelatin patch (RapiSealTM) for use in pulmonary surgery to seal air leaks, and in solid abdominal organ surgeries to provide hemostatic tamponade. The new electrode allows for the application of RF energy in contact mode without the problems of the electrode sticking to the gelatin patch or the underlying tissue. Designed for use with commercially available electrosurgical handpieces, the electrode consists of a stainless steel connector that fits into the hand- piece, and an electrode assembly made from silver that includes a shank region, and a tip extension extending distally from the shank region. The distal tip of the tip extension is rounded and has a length of about 10 mm. The uniqueness of this electrode is the shank region which has a cross sectional area that is larger than the tip extension. The shank region acts as a heat sink to draw away heat from the tip extension while the tip extension itself remains sufficiently small to access desired target sites and display the desired energy transfer properties. In addition to the physical design, the use of silver as the core element provides a material with high electrical and thermal conductivities. The bulk of the electrode is appropriately insulated.

  10. Structural materials research for lighter-than-air systems

    NASA Technical Reports Server (NTRS)

    Alley, V. L., Jr.; Mchatton, A. D.

    1975-01-01

    Inflatable systems have widespread applications in military, government, and industrial sectors. Improvements in inflatable materials have followed each salient advancement in textiles. The new organic fiber, Kevlar, is a recent and most significant advancement that justified reexamination of old and new inflatable materials' applications. A fertile frontier exists in integrating Kevlar with various other material combinations, in optimization of geometric features, and in selection of thermomechanical characteristics' compatibility with the environment. Expectations regarding Kevlar have been justified by the performance of two experimental materials. Styrene-butadiene-styrene block copolymers appear promising as a constituent adhesive for low temperature applications. Biaxial testing for both strength and material elastic properties is a technology area needing greater awareness and technology growth along with improved facilities. Because of dramatic materials' advancements, inflatable systems appear to be moving toward an increased position in tomorrow's aerospace industry.

  11. Controlled porosity in electrodes

    SciTech Connect

    Chiang, Yet-Ming; Bae, Chang-Jun; Halloran, John William; Fu, Qiang; Tomsia, Antoni P.; Erdonmez, Can K.

    2015-06-23

    Porous electrodes in which the porosity has a low tortuosity are generally provided. In some embodiments, the porous electrodes can be designed to be filled with electrolyte and used in batteries, and can include low tortuosity in the primary direction of ion transport during charge and discharge of the battery. In some embodiments, the electrodes can have a high volume fraction of electrode active material (i.e., low porosity). The attributes outlined above can allow the electrodes to be fabricated with a higher energy density, higher capacity per unit area of electrode (mAh/cm.sup.2), and greater thickness than comparable electrodes while still providing high utilization of the active material in the battery during use. Accordingly, the electrodes can be used to produce batteries with high energy densities, high power, or both compared to batteries using electrodes of conventional design with relatively highly tortuous pores.

  12. FeS/nickel foam as stable and efficient counter electrode material for quantum dot sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Geng, Huifang; Zhu, Liqun; Li, Weiping; Liu, Huicong; Quan, Linlin; Xi, Fanxing; Su, Xunwen

    2015-05-01

    A stable and efficient FeS/nickel foam (NF) counter electrode for quantum dots-sensitized solar cells (QDSCs) is first fabricated by electrochemistry deposition and characterized with scanning electron microscope (SEM), X-ray photoelectron spectroscopy (XPS), current voltage and impedance spectroscopy. The QDSC based on FeS/NF CE achieves a power conversion efficiency (PCE) of 4.39% attributing to the high fill factor (FF) of 0.58, and the PCE is much higher than that of based on FeS/FTO CE (2.76%) and other reported FeS CEs (1.76% and 3.34%). The phenomenon that the electrode can transform between FeS/NF (in the polysulfide electrolyte) and Fe2O3/NF (in the air) spontaneously is first reported. And the excellent stability in photoelectric performance of the CE is also demonstrated in the present work. Therefore, the FeS/NF is very promising as a stable and efficient CE for QDSCs.

  13. Supercapacitor electrode based on mixtures of graphene/graphite and carbon nanotubes fabricated using a new dynamic air-brush deposition technique

    NASA Astrophysics Data System (ADS)

    Bondavalli, P.; Delfaure, C.; Pribat, D.; Legagneux, P.

    2013-09-01

    This contribution deals with the fabrication of electrode and supercapacitor cell using a new dynamic air-brush deposition technique. This method allows to achieve extremely (ou highly) uniform mats with finely tuned thickness and weight in a completely reproducible way. Using this deposition technique, we have analyzed the effect of mixture of CNTs and graphene/graphite on the electrode and cell properties (energy, power and capacitance). using a mixture of 75% of graphene/graphite and 25% of CNTs we increased the power by a factor 2.5 compared to bare CNTs based electrodes. We also analyzed the effect of the weight firstly on the capacitance and specific energy and then on the specific power. We were able to reach a specific power of 200kW/Kg and a specific energy of 9.1Wh/Kg with an electrode having a surface of 2cm2 and a weight of 0.25mg composed by 50% of CNTs and graphene/graphite (using a common aqueous electrolyte). using our deposition technique we are able to achieve supercapacitors with ad-hoc characteristics simply modulating the weight and the concentration of the mixture in a completely reproducible way.

  14. Nonlinear air-coupled emission: The signature to reveal and image microdamage in solid materials

    SciTech Connect

    Solodov, Igor; Busse, Gerd

    2007-12-17

    It is shown that low-frequency elastic vibrations of near-surface planar defects cause high-frequency ultrasonic radiation in surrounding air. The frequency conversion mechanism is concerned with contact nonlinearity of the defect vibrations and provides efficient generation of air-coupled higher-order ultraharmonics, ultrasubharmonics, and combination frequencies. The nonlinear air-coupled ultrasonic emission is applied for location and high-resolution imaging of damage-induced defects in a variety of solid materials.

  15. Production of atmospheric pressure diffuse nanosecond pulsed dielectric barrier discharge using the array needles-plate electrode in air

    SciTech Connect

    Yang Dezheng; Wang Wenchun; Jia Li; Nie Dongxia; Shi Hengchao

    2011-04-01

    In this paper, a bidirectional high pulse voltage with 20 ns rising time is employed to generate an atmospheric pressure diffuse dielectric barrier discharge using the array needles-plate electrode configuration. Both double needle and multiple needle electrode configurations nanosecond pulsed dielectric barrier discharges are investigated. It is found that a diffuse discharge plasma with low gas temperature can be obtained, and the plasma volume increases with the increase of the pulse peak voltage, but remains almost constant with the increase of the pulse repetition rate. In addition to showing the potential application on a topographically nonuniform surface treatment of the discharge, the multiple needle-plate electrode configuration with different needle-plate electrode gaps are also employed to generate diffuse discharge plasma.

  16. Production of an ion-exchange membrane-catalytic electrode bonded material for electrolytic cells

    NASA Technical Reports Server (NTRS)

    Takenaka, H.; Torikai, E.

    1986-01-01

    A good bond is achieved by placing a metal salt in solution on one side of a membrane and a reducing agent on the other side so that the reducing agent penetrates the membrane and reduces the metal. Thus, a solution containing Pt, Rh, etc., is placed on one side of the membrane and a reducing agent such as NaBH, is placed on the other side. The bonded metal layer obtained is superior in catalytic activity and is suitable as an electrode in a cell such as for solid polymer electrolyte water electrolysis.

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

    NASA Astrophysics Data System (ADS)

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

    2016-04-01

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

  18. Material Properties from Air Puff Corneal Deformation by Numerical Simulations on Model Corneas

    PubMed Central

    Dorronsoro, Carlos; de la Hoz, Andrés; Marcos, Susana

    2016-01-01

    Objective To validate a new method for reconstructing corneal biomechanical properties from air puff corneal deformation images using hydrogel polymer model corneas and porcine corneas. Methods Air puff deformation imaging was performed on model eyes with artificial corneas made out of three different hydrogel materials with three different thicknesses and on porcine eyes, at constant intraocular pressure of 15 mmHg. The cornea air puff deformation was modeled using finite elements, and hyperelastic material parameters were determined through inverse modeling, minimizing the difference between the simulated and the measured central deformation amplitude and central-peripheral deformation ratio parameters. Uniaxial tensile tests were performed on the model cornea materials as well as on corneal strips, and the results were compared to stress-strain simulations assuming the reconstructed material parameters. Results The measured and simulated spatial and temporal profiles of the air puff deformation tests were in good agreement (< 7% average discrepancy). The simulated stress-strain curves of the studied hydrogel corneal materials fitted well the experimental stress-strain curves from uniaxial extensiometry, particularly in the 0–0.4 range. Equivalent Young´s moduli of the reconstructed material properties from air-puff were 0.31, 0.58 and 0.48 MPa for the three polymer materials respectively which differed < 1% from those obtained from extensiometry. The simulations of the same material but different thickness resulted in similar reconstructed material properties. The air-puff reconstructed average equivalent Young´s modulus of the porcine corneas was 1.3 MPa, within 18% of that obtained from extensiometry. Conclusions Air puff corneal deformation imaging with inverse finite element modeling can retrieve material properties of model hydrogel polymer corneas and real corneas, which are in good correspondence with those obtained from uniaxial extensiometry

  19. Au-embedded ZnO/NiO hybrid with excellent electrochemical performance as advanced electrode materials for supercapacitor.

    PubMed

    Zheng, Xin; Yan, Xiaoqin; Sun, Yihui; Bai, Zhiming; Zhang, Guangjie; Shen, Yanwei; Liang, Qijie; Zhang, Yue

    2015-02-01

    Here we design a nanostructure by embedding Au nanoparticles into ZnO/NiO core-shell composites as supercapacitors electrodes materials. This optimized hybrid electrodes exhibited an excellent electrochemical performance including a long-term cycling stability and a maximum specific areal capacitance of 4.1 F/cm(2) at a current density of 5 mA/cm(2), which is much higher than that of ZnO/NiO hierarchical materials (0.5 F/cm(2)). Such an enhanced property is attributed to the increased electro-electrolyte interfaces, short electron diffusion pathways and good electrical conductivity. Apart from this, electrons can be temporarily trapped and accumulated at the Fermi level (EF') because of the localized schottky barrier at Au/NiO interface in charge process until fill the gap between ZnO and NiO, so that additional electrons can be released during discharge. These results demonstrate that suitable interface engineering may open up new opportunities in the development of high-performance supercapacitors.

  20. Absolute OH density measurements in an atmospheric pressure dc glow discharge in air with water electrode by broadband UV absorption spectroscopy

    NASA Astrophysics Data System (ADS)

    Xiong, Qing; Yang, Zhiqiang; Bruggeman, Peter J.

    2015-10-01

    Spatially resolved absolute OH radical density measurements are performed in an atmospheric pressure glow discharge generated in ambient air with water electrode by broadband UV absorption spectroscopy. The radial distributions of OH density and gas temperature are obtained for the positive column, anode and cathode regions both for water-cathode and water-anode discharges. It is found that for both polarities of the water electrode the radial profiles of the ground state OH density and gas temperature are significantly broader than the total discharge emission intensity and the emission intensity originating from OH(\\text{A}{}2{{\\text{ }Σ\\text{ }}+} ) only. Exceptional large OH densities exceeding 1023 m-3 are found. The OH kinetics are discussed in detail.

  1. 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.

  2. Recent advances in the efficient reduction of graphene oxide and its application as energy storage electrode materials

    NASA Astrophysics Data System (ADS)

    Kuila, Tapas; Mishra, Ananta Kumar; Khanra, Partha; Kim, Nam Hoon; Lee, Joong Hee

    2012-12-01

    Efficient reduction of graphene oxide (GO) by chemical, thermal, electrochemical, and photo-irradiation techniques has been reviewed. Particular emphasis has been directed towards the proposed reduction mechanisms of GO by different reducing agents and techniques. The advantages of using different kinds of reducing agents on the basis of their availability, cost-effectiveness, toxicity, and easy product isolation processes have also been studied extensively. We provide a detailed description of the improvement in physiochemical properties of reduced GO (RGO) compared to pure GO. For example, the electrical conductivity and electrochemical performance of electrochemically obtained RGO are much better than those of chemically or thermally RGO materials. We provide examples of how RGO has been used as supercapacitor electrode materials. Specific capacitance of GO increases after reduction and the value has been reported to be 100-300 F g-1. We conclude by proposing new environmentally friendly types of reducing agents that can efficiently remove oxygen functionalities from the surface of GO.

  3. Use of cooling air heat exchangers as replacements for hot section strategic materials

    NASA Technical Reports Server (NTRS)

    Gauntner, J. W.

    1983-01-01

    Because of financial and political constraints, strategic aerospace materials required for the hot section of future engines might be in short supply. As an alternative to these strategic materials, this study examines the use of a cooling air heat exchanger in combination with less advanced hot section materials. Cycle calculations are presented for future turbofan systems with overall pressure ratios to 65, bypass ratios near 13, and combustor exit temperatures to 3260 R. These calculations quantify the effect on TSFC of using a decreased materials technology in a turbofan system. The calculations show that the cooling air heat exchanger enables the feasibility of these engines.

  4. 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.

  5. A facile synthesis of graphene foam as electrode material for supercapacitor

    NASA Astrophysics Data System (ADS)

    Sivaprakash, S.; Sivaprakash, Prabhavathy

    2016-07-01

    We report here a versatile fabrication approach of graphene foam (GF) with three dimensional (3D) porous conductive networks which reveal great potential for application in energy storage devices. This facile fabrication technique is believed to be favorable for supercapacitor application as the 3D-GF comprises conductive continuous porous networks with large active surface area. Supercapacitors utilize this high surface area electrode to attain improved capacitance. The resulting graphene foam exhibited satisfactory double layer capacitive behavior with improved electrochemical performance having good electrochemical cycling stability and high specific capacitance of 310 F g-1 at current density of 5 A g-1 and 160 F g-1 at current density of 20 A g-1.

  6. Insulated ECG electrodes

    NASA Technical Reports Server (NTRS)

    Portnoy, W. M.; David, R. M.

    1973-01-01

    Insulated, capacitively coupled electrode does not require electrolyte paste for attachment. Other features of electrode include wide range of nontoxic material that may be employed for dielectric because of sputtering technique used. Also, electrode size is reduced because there is no need for external compensating networks with FET operational amplifier.

  7. Solid-state sodium batteries using polymer electrolytes and sodium intercalation electrode materials

    SciTech Connect

    Ma, Y. |

    1996-08-01

    Solid-state sodium cells using polymer electrolytes (polyethylene oxide mixed with sodium trifluoromethanesulfonate: PEO{sub n}NaCF{sub 3}SO{sub 3}) and sodium cobalt oxide positive electrodes are characterized in terms of discharge and charge characteristics, rate capability, cycle life, and energy and power densities. The P2 phase Na{sub x}CoO{sub 2} can reversibly intercalate sodium in the range of x = 0.3 to 0.9, giving a theoretical specific energy of 440 Wh/kg and energy density of 1,600 Wh/l. Over one hundred cycles to 60% depth of discharge have been obtained at 0.5 mA/cm{sup 2}. Experiments show that the electrolyte/Na interface is stable and is not the limiting factor to cell cycle life. Na{sub 0.7}CoO{sub 2} composite electrodes containing various amounts of carbon black additive are investigated. The transport properties of polymer electrolytes are the critical factors for performance. These properties (the ionic conductivity, salt diffusion coefficient, and ion transference number) are measured for the PEO{sub n}NaCF{sub 3}SO{sub 3} system over a wide range of concentrations at 85 C. All the three transport properties are very salt-concentration dependent. The ionic conductivity exhibits a maximum at about n = 20. The transference number, diffusion coefficient, and thermodynamic factor all vary with salt concentration in a similar fashion, decreasing as the concentration increases, except for a local maximum. These results verify that polymer electrolytes cannot be treated as ideal solutions. The measured transport-property values are used to analyze and optimize the electrolytes by computer simulation and also cell testing. Salt precipitation is believed to be the rate limiting process for cells using highly concentrated solutions, as a result of lower values of these properties, while salt depletion is the limiting factor when a dilute solution is used.

  8. Air-coupled ultrasonic evaluation of food materials.

    PubMed

    Pallav, P; Hutchins, D A; Gan, T H

    2009-02-01

    This research was performed with the aim of detecting foreign bodies and additives within food products, and to measure selected acoustic properties, without contact to the sample. This would allow use in manufacturing plants on production lines, where contacting the product for ultrasonic inspection would not be feasible. Images of internal structure are reported. The air-coupled system uses capacitive devices which are able to provide sufficient bandwidth for many measurements, including the detection of foreign bodies in cheese, the detection of deliberate additives to chocolate, the detection of fill level and content of metallic food cans, and measurements of frozen dough products. The approach demonstrates that ultrasound has the potential for application to many industrial food packaging environments where non-metallic objects within food need to be detected. PMID:18973911

  9. High frequency reference electrode

    DOEpatents

    Kronberg, James W.

    1994-01-01

    A high frequency reference electrode for electrochemical experiments comprises a mercury-calomel or silver-silver chloride reference electrode with a layer of platinum around it and a layer of a chemically and electrically resistant material such as TEFLON around the platinum covering all but a small ring or "halo" at the tip of the reference electrode, adjacent to the active portion of the reference electrode. The voltage output of the platinum layer, which serves as a redox electrode, and that of the reference electrode are coupled by a capacitor or a set of capacitors and the coupled output transmitted to a standard laboratory potentiostat. The platinum may be applied by thermal decomposition to the surface of the reference electrode. The electrode provides superior high-frequency response over conventional electrodes.

  10. High frequency reference electrode

    DOEpatents

    Kronberg, J.W.

    1994-05-31

    A high frequency reference electrode for electrochemical experiments comprises a mercury-calomel or silver-silver chloride reference electrode with a layer of platinum around it and a layer of a chemically and electrically resistant material such as TEFLON around the platinum covering all but a small ring or halo' at the tip of the reference electrode, adjacent to the active portion of the reference electrode. The voltage output of the platinum layer, which serves as a redox electrode, and that of the reference electrode are coupled by a capacitor or a set of capacitors and the coupled output transmitted to a standard laboratory potentiostat. The platinum may be applied by thermal decomposition to the surface of the reference electrode. The electrode provides superior high-frequency response over conventional electrodes. 4 figs.

  11. AIR EMISSIONS FROM LASER DRILLING OF PRINTED WIRING BOARD MATERIALS

    EPA Science Inventory

    The paper gives results of a study to characterize gases generated during laser drilling of printed wiring board (PWB) material and identifies the pollutants and generation rates found during the drilling process. Typically found in the missions stream were trace amounts of carbo...

  12. Magnetohydrodynamic electrode

    DOEpatents

    Marchant, David D.; Killpatrick, Don H.

    1978-01-01

    An electrode capable of withstanding high temperatures and suitable for use as a current collector in the channel of a magnetohydrodynamic (MHD) generator consists of a sintered powdered metal base portion, the upper surface of the base being coated with a first layer of nickel aluminide, an intermediate layer of a mixture of nickel aluminide - refractory ceramic on the first layer and a third or outer layer of a refractory ceramic material on the intermediate layer. The sintered powdered metal base resists spalling by the ceramic coatings and permits greater electrode compliance to thermal shock. The density of the powdered metal base can be varied to allow optimization of the thermal conductivity of the electrode and prevent excess heat loss from the channel.

  13. Solid-State Electrode Engineering and Material Processing for All-Solid-State Lithium and Lithium-Ion Batteries

    NASA Astrophysics Data System (ADS)

    Yersak, Thomas A.

    In this dissertation we demonstrate the full rechargeability of a FeS 2/lithium metal battery at 60°C. To enable the reversibility of the FeS2 redox chemistry we utilize a bulk all-solid-state battery architecture based upon the Li2S-P2S5 glass-ceramic electrolyte. The glass-ceramic electrolyte's non-volatility and non-flammability allows us to use a lithium metal anode safely, while its solid nature confines FeS2's intermediate electroactive species to prevent active material loss and capacity fade. Based only on the weight of the active materials our battery stands to triple the specific energy (Wh kg-1) of conventional state-of-the-art Li-ion batteries. We also observe ortho-FeS2 as a charge product and propose a new discharge mechanism which revises 30 years of research on the subject. Unfortunately, our laboratory FeS2/Li battery could not achieve a practical cell-level specific energy because the composite electrode was nearly 70 wt. % glass-ceramic electrolyte and carbon black. We also found that our batteries were not durable because the formation of lithium dendrites through the glass-ceramic electrolyte separator membrane frequently internally shorted test cells upon charge. The remainder of this dissertation outlines our work to develop an all-solid-state Li-ion battery to address the shorting issue and the work done to engineer better active material-electrolyte solid-solid interfaces in the composite electrode for high cell-level specific energy.

  14. Effect of dielectric material on bipolar nanosecond pulse diffuse dielectric barrier discharge in air at atmospheric pressure.

    PubMed

    Tang, Kai; Wang, Wenchun; Yang, Dezheng; Zhang, Shuai; Yang, Yang; Liu, Zhijie

    2013-08-01

    In this paper, dielectric plates made by ceramic, quartz and polytetrafluoroethylene (PTFE) respectively are employed to generate low gas temperature, diffuse dielectric barrier discharge plasma by using a needle-plate electrode configuration in air at atmospheric pressure. Both discharge images and the optical emission spectra are obtained while ceramic, quartz and PTFE are used as dielectric material. Plasma gas temperature is also calculated by comparing the experimental emission spectra with the best fitted spectra of N2 (C(3)Πu→B(3)Πg 1-3) and N2 (C(3)Πu→B(3)Πg 0-2). The effects of different pulse peak voltages and gas gap distances on the emission intensity of N2 (C(3)Πu→B(3)Πg, 0-0, 337.1 nm) and the plasma area on dielectric surface are investigated while ceramic, quartz and PTFE are used as dielectric material. It is found that the permittivity of dielectric material plays an important role in the discharge homogeneity, plasma gas temperature, emission spectra intensity of the discharge, etc. Dielectric with higher permittivity i.e., ceramic means brighter discharge luminosity and stronger emission spectra intensity of N2 (C(3)Πu→B(3)Πg, 0-0, 337.1 nm) among the three dielectric materials. However, more homogeneous, larger plasma area on dielectric surface and lower plasma gas temperature can be obtained under dielectric with lower permittivity i.e., PTFE. The emission spectra intensity and plasma gas temperature of the discharge while the dielectric plate is made by quartz are smaller than that while ceramic is used as dielectric material and bigger than that when PTFE is used as dielectric material.

  15. Effect of dielectric material on bipolar nanosecond pulse diffuse dielectric barrier discharge in air at atmospheric pressure

    NASA Astrophysics Data System (ADS)

    Tang, Kai; Wang, Wenchun; Yang, Dezheng; Zhang, Shuai; Yang, Yang; Liu, Zhijie

    2013-08-01

    In this paper, dielectric plates made by ceramic, quartz and polytetrafluoroethylene (PTFE) respectively are employed to generate low gas temperature, diffuse dielectric barrier discharge plasma by using a needle-plate electrode configuration in air at atmospheric pressure. Both discharge images and the optical emission spectra are obtained while ceramic, quartz and PTFE are used as dielectric material. Plasma gas temperature is also calculated by comparing the experimental emission spectra with the best fitted spectra of N2 (C3Πu → B3Πg 1-3) and N2 (C3Πu → B3Πg 0-2). The effects of different pulse peak voltages and gas gap distances on the emission intensity of N2 (C3Πu → B3Πg, 0-0, 337.1 nm) and the plasma area on dielectric surface are investigated while ceramic, quartz and PTFE are used as dielectric material. It is found that the permittivity of dielectric material plays an important role in the discharge homogeneity, plasma gas temperature, emission spectra intensity of the discharge, etc. Dielectric with higher permittivity i.e., ceramic means brighter discharge luminosity and stronger emission spectra intensity of N2 (C3Πu → B3Πg, 0-0, 337.1 nm) among the three dielectric materials. However, more homogeneous, larger plasma area on dielectric surface and lower plasma gas temperature can be obtained under dielectric with lower permittivity i.e., PTFE. The emission spectra intensity and plasma gas temperature of the discharge while the dielectric plate is made by quartz are smaller than that while ceramic is used as dielectric material and bigger than that when PTFE is used as dielectric material.

  16. Effect of dielectric material on bipolar nanosecond pulse diffuse dielectric barrier discharge in air at atmospheric pressure.

    PubMed

    Tang, Kai; Wang, Wenchun; Yang, Dezheng; Zhang, Shuai; Yang, Yang; Liu, Zhijie

    2013-08-01

    In this paper, dielectric plates made by ceramic, quartz and polytetrafluoroethylene (PTFE) respectively are employed to generate low gas temperature, diffuse dielectric barrier discharge plasma by using a needle-plate electrode configuration in air at atmospheric pressure. Both discharge images and the optical emission spectra are obtained while ceramic, quartz and PTFE are used as dielectric material. Plasma gas temperature is also calculated by comparing the experimental emission spectra with the best fitted spectra of N2 (C(3)Πu→B(3)Πg 1-3) and N2 (C(3)Πu→B(3)Πg 0-2). The effects of different pulse peak voltages and gas gap distances on the emission intensity of N2 (C(3)Πu→B(3)Πg, 0-0, 337.1 nm) and the plasma area on dielectric surface are investigated while ceramic, quartz and PTFE are used as dielectric material. It is found that the permittivity of dielectric material plays an important role in the discharge homogeneity, plasma gas temperature, emission spectra intensity of the discharge, etc. Dielectric with higher permittivity i.e., ceramic means brighter discharge luminosity and stronger emission spectra intensity of N2 (C(3)Πu→B(3)Πg, 0-0, 337.1 nm) among the three dielectric materials. However, more homogeneous, larger plasma area on dielectric surface and lower plasma gas temperature can be obtained under dielectric with lower permittivity i.e., PTFE. The emission spectra intensity and plasma gas temperature of the discharge while the dielectric plate is made by quartz are smaller than that while ceramic is used as dielectric material and bigger than that when PTFE is used as dielectric material. PMID:23673240

  17. Facile Self-Cross-Linking Synthesis of 3D Nanoporous Co3O4/Carbon Hybrid Electrode Materials for Supercapacitors.

    PubMed

    Wang, Ning; Liu, Qinglei; Kang, Danmiao; Gu, Jiajun; Zhang, Wang; Zhang, Di

    2016-06-29

    A hybrid electrode material with ultrafine Co3O4 nanoparticles embedded throughout a hierarchically nanoporous graphitic carbon matrix has been obtained via a facile self-cross-linking route. Sodium alginate, a biopolymer with an ability of cross-linking with multivalent cobalt cations to form ordered microcrystalline zones, is used as a carbon source to produce nanoporous carbon frameworks of the hybrids. Ultrafine Co3O4 nanoparticles with tunable particle size (3-30 nm) are in situ grown within the nanoporous graphitic carbon frameworks by a simple carbonization of Co-cross-linked alginate. The obtained hybrid electrodes exhibit high specific capacitance of 645, 548, 486, and 347 F/g at scan rates of 5, 10, 20, and 50 mV/s, respectively, and excellent cycle performance with only 1% fading in capacitance after 10 000 cycles at a high current density of 20 A/g. Such excellent capacitive performance is ascribed to the collaborative contributions of well-dispersed ultrafine Co3O4 nanoparticles and conductive nanoporous carbon frameworks. PMID:27266717

  18. Conductive porous sponge-like ionic liquid-graphene assembly decorated with nanosized polyaniline as active electrode material for supercapacitor

    NASA Astrophysics Data System (ADS)

    Halab Shaeli Iessa, K.; Zhang, Yan; Zhang, Guoan; Xiao, Fei; Wang, Shuai

    2016-01-01

    We report the development of three-dimensional (3D) porous sponge-like ionic liquid (IL)-graphene hybrid material by integrating IL molecules and graphene nanosheets via self-assembly process. The as-obtained IL-graphene architecture possesses high surface area, efficient electron transport network and fast charge transfer kinetics owing to its highly porous structure, and unique hydrophilic properties derived from the IL anion on its surface, which endows it with high desire for supercapacitor application. Redox-active polyaniline (PANI) nanorods are further decorated on IL-graphene scaffold by electropolymerization. When utilized as freestanding 3D electrode for supercapacitor, the resultant PANI modified IL-graphene (PANI-IL-graphene) electrode exhibits a specific capacitance up to 662 F g-1 at the current density of 1.0 A g-1, with a high capacitance retention of 73.7% as current densities increase from 1.0 to 20 A g-1, and the capacitance degradation is less than 7.0% after 5000 charge-discharge cycles at 10 A g-1.

  19. Direct Observation of Active Material Concentration Gradients and Crystallinity Breakdown in LiFePO4 Electrodes During Charge/Discharge Cycling of Lithium Batteries

    PubMed Central

    2014-01-01

    The phase changes that occur during discharge of an electrode comprised of LiFePO4, carbon, and PTFE binder have been studied in lithium half cells by using X-ray diffraction measurements in reflection geometry. Differences in the state of charge between the front and the back of LiFePO4 electrodes have been visualized. By modifying the X-ray incident angle the depth of penetration of the X-ray beam into the electrode was altered, allowing for the examination of any concentration gradients that were present within the electrode. At high rates of discharge the electrode side facing the current collector underwent limited lithium insertion while the electrode as a whole underwent greater than 50% of discharge. This behavior is consistent with depletion at high rate of the lithium content of the electrolyte contained in the electrode pores. Increases in the diffraction peak widths indicated a breakdown of crystallinity within the active material during cycling even during the relatively short duration of these experiments, which can also be linked to cycling at high rate. PMID:24790684

  20. Compartmented electrode structure

    DOEpatents

    Vissers, Donald R.; Shimotake, Hiroshi; Gay, Eddie C.; Martino, Fredric J.

    1977-06-14

    Electrodes for secondary electrochemical cells are provided with compartments for containing particles of the electrode reactant. The compartments are defined by partitions that are generally impenetrable to the particles of reactant and, in some instances, to the liquid electrolyte used in the cell. During cycling of the cell, reactant material initially loaded into a particular compartment is prevented from migrating and concentrating within the lower portion of the electrode or those portions of the electrode that exhibit reduced electrical resistance.

  1. Non-Print Instructional Materials for the Air Conditioning and Refrigeration Maintenance Field.

    ERIC Educational Resources Information Center

    Golitko, Raymond L., Ed.; And Others

    This catalog contains a listing of air conditioning/refrigeration maintenance audiovisual training materials from the Houston Community College System library media collection. The material is organized by subject heading. The media titles are listed in alphabetical order by title under each subject heading in the catalog. The citation for each…

  2. Aerosol jet printed p- and n-type electrolyte-gated transistors with a variety of electrode materials: exploring practical routes to printed electronics.

    PubMed

    Hong, Kihyon; Kim, Se Hyun; Mahajan, Ankit; Frisbie, C Daniel

    2014-11-12

    Printing electrically functional liquid inks is a promising approach for achieving low-cost, large-area, additive manufacturing of flexible electronic circuits. To print thin-film transistors, a basic building block of thin-film electronics, it is important to have several options for printable electrode materials that exhibit high conductivity, high stability, and low-cost. Here we report completely aerosol jet printed (AJP) p- and n-type electrolyte-gated transistors (EGTs) using a variety of different electrode materials including highly conductive metal nanoparticles (Ag), conducting polymers (polystyrenesulfonate doped poly(3,4-ethylendedioxythiophene, PEDOT:PSS), transparent conducting oxides (indium tin oxide), and carbon-based materials (reduced graphene oxide). Using these source-drain electrode materials and a PEDOT:PSS/ion gel gate stack, we demonstrated all-printed p- and n-type EGTs in combination with poly(3-hexythiophene) and ZnO semiconductors. All transistor components (including electrodes, semiconductors, and gate insulators) were printed by AJP. Both kinds of devices showed typical p- and n-type transistor characteristics, and exhibited both low-threshold voltages (<2 V) and high hole and electron mobilities. Our assessment suggests Ag electrodes may be the best option in terms of overall performance for both types of EGTs.

  3. Hierarchical Heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) as an Electrode Material for High-Performance Supercapacitors.

    PubMed

    Hu, Jiyu; Qian, Feng; Song, Guosheng; Wang, Linlin

    2016-12-01

    Hierarchical heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) were developed as an electrode material for supercapacitor with improved pseudocapacitive performance. Within these hierarchical heterostructures, the mesoporous NiCo2O4 nanosheet arrays directly grown on the Ni foam can not only act as an excellent pseudocapacitive material but also serve as a hierarchical scaffold for growing NiMoO4 or CoMoO4 electroactive materials (nanosheets). The electrode made of NiCo2O4@NiMoO4 presented a highest areal capacitance of 3.74 F/cm(2) at 2 mA/cm(2), which was much higher than the electrodes made of NiCo2O4@CoMoO4 (2.452 F/cm(2)) and NiCo2O4 (0.456 F/cm(2)), respectively. Meanwhile, the NiCo2O4@NiMoO4 electrode exhibited good rate capability. It suggested the potential of the hierarchical heterostructures of NiCo2O4@CoMoO4 as an electrode material in supercapacitors.

  4. Hierarchical Heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) as an Electrode Material for High-Performance Supercapacitors

    NASA Astrophysics Data System (ADS)

    Hu, Jiyu; Qian, Feng; Song, Guosheng; Wang, Linlin

    2016-05-01

    Hierarchical heterostructures of NiCo2O4@XMoO4 (X = Ni, Co) were developed as an electrode material for supercapacitor with improved pseudocapacitive performance. Within these hierarchical heterostructures, the mesoporous NiCo2O4 nanosheet arrays directly grown on the Ni foam can not only act as an excellent pseudocapacitive material but also serve as a hierarchical scaffold for growing NiMoO4 or CoMoO4 electroactive materials (nanosheets). The electrode made of NiCo2O4@NiMoO4 presented a highest areal capacitance of 3.74 F/cm2 at 2 mA/cm2, which was much higher than the electrodes made of NiCo2O4@CoMoO4 (2.452 F/cm2) and NiCo2O4 (0.456 F/cm2), respectively. Meanwhile, the NiCo2O4@NiMoO4 electrode exhibited good rate capability. It suggested the potential of the hierarchical heterostructures of NiCo2O4@CoMoO4 as an electrode material in supercapacitors.

  5. Preparation of Fiber Based Binder Materials to Enhance the Gas Adsorption Efficiency of Carbon Air Filter.

    PubMed

    Lim, Tae Hwan; Choi, Jeong Rak; Lim, Dae Young; Lee, So Hee; Yeo, Sang Young

    2015-10-01

    Fiber binder adapted carbon air filter is prepared to increase gas adsorption efficiency and environmental stability. The filter prevents harmful gases, as well as particle dusts in the air from entering the body when a human inhales. The basic structure of carbon air filter is composed of spunbond/meltblown/activated carbon/bottom substrate. Activated carbons and meltblown layer are adapted to increase gas adsorption and dust filtration efficiency, respectively. Liquid type adhesive is used in the conventional carbon air filter as a binder material between activated carbons and other layers. However, it is thought that the liquid binder is not an ideal material with respect to its bonding strength and liquid flow behavior that reduce gas adsorption efficiency. To overcome these disadvantages, fiber type binder is introduced in our study. It is confirmed that fiber type binder adapted air filter media show higher strip strength, and their gas adsorption efficiencies are measured over 42% during 60 sec. These values are higher than those of conventional filter. Although the differential pressure of fiber binder adapted air filter is relatively high compared to the conventional one, short fibers have a good potential as a binder materials of activated carbon based air filter.

  6. Entropy change characteristics of LiMn0.67Fe0.33PO4 and Li4Ti5O12 electrode materials

    NASA Astrophysics Data System (ADS)

    Jalkanen, K.; Vuorilehto, K.

    2015-01-01

    The combination of LiMn0.67Fe0.33PO4 positive and Li4Ti5O12 negative electrode is studied in terms of its entropy change behavior, which affects the reversible heat generation of a lithium-ion cell. This electrode combination is especially interesting for large applications, as it is proposed to be a very safe choice having still an adequate energy density. The entropy change of LiMn0.67Fe0.33PO4 and Li4Ti5O12 electrode materials is measured at different states of charge using a potentiometric method. The results are compared with conventional electrode materials, LiFePO4 and artificial graphite. The entropy change of LiMn0.67Fe0.33PO4 is found to follow the distinct plateaus of Fe2+/Fe3+ and Mn2+/Mn3+ redox couples and to be clearly different from LiFePO4. This difference is suggested to be due to single-phase solid solution regions, originating from effects of substituting Mn for Fe. For Li4Ti5O12, mostly a constant entropy change typical for a two-phase reaction is observed, except for the region near 0% state of charge. The data from individual electrodes is used to simulate and compare the entropy change behavior and thus the reversible heat generation rate of different electrode combinations.

  7. Electrical Characteristics, Electrode Sheath and Contamination Layer Behavior of a Meso-Scale Premixed Methane-Air Flame Under AC/DC Electric Fields

    NASA Astrophysics Data System (ADS)

    Chen, Qi; Yan, Limin; Zhang, Hao; Li, Guoxiu

    2016-05-01

    Electrical characteristics of a nozzle-attached meso-scale premixed methane-air flame under low-frequency AC (0-4300 V, 0-500 Hz) and DC (0-3300 V) electric fields were studied. I-V curves were measured under different experimental conditions to estimate the magnitude of the total current 100-102 μA, the electron density 1015-1016 m-3 and further the power dissipation ≤ 0.7 W in the reaction zone. At the same time, the meso-scale premixed flame conductivity 10-4-10-3 Ω-1·m-1 as a function of voltage and frequency was experimentally obtained and was believed to represent a useful order-of magnitude estimate. Moreover, the influence of the collision sheath relating to Debye length (31-98 μm) and the contamination layer of an active electrode on measurements was discussed, based on the combination of simulation and theoretical analysis. As a result, the electrode sheath dimension was evaluated to less than 0.5 mm, which indicated a complex effect of the collision sheath on the current measurements. The surface contamination effect of an active electrode was further analyzed using the SEM imaging method, which showed elements immigration during the contamination layer formation process. supported by National Natural Science Foundation of China (No. 51376021), and the Fundamental Research Fund for Major Universities (No. 2013JBM079)

  8. Electrical Characteristics, Electrode Sheath and Contamination Layer Behavior of a Meso-Scale Premixed Methane-Air Flame Under AC/DC Electric Fields

    NASA Astrophysics Data System (ADS)

    Chen, Qi; Yan, Limin; Zhang, Hao; Li, Guoxiu

    2016-05-01

    Electrical characteristics of a nozzle-attached meso-scale premixed methane-air flame under low-frequency AC (0-4300 V, 0-500 Hz) and DC (0-3300 V) electric fields were studied. I-V curves were measured under different experimental conditions to estimate the magnitude of the total current 100-102 μA, the electron density 1015-1016 m‑3 and further the power dissipation ≤ 0.7 W in the reaction zone. At the same time, the meso-scale premixed flame conductivity 10‑4-10‑3 Ω‑1·m‑1 as a function of voltage and frequency was experimentally obtained and was believed to represent a useful order-of magnitude estimate. Moreover, the influence of the collision sheath relating to Debye length (31–98 μm) and the contamination layer of an active electrode on measurements was discussed, based on the combination of simulation and theoretical analysis. As a result, the electrode sheath dimension was evaluated to less than 0.5 mm, which indicated a complex effect of the collision sheath on the current measurements. The surface contamination effect of an active electrode was further analyzed using the SEM imaging method, which showed elements immigration during the contamination layer formation process. supported by National Natural Science Foundation of China (No. 51376021), and the Fundamental Research Fund for Major Universities (No. 2013JBM079)

  9. Interphase evolution at two promising electrode materials for Li-ion batteries: LiFePO4 and LiNi1/2 Mn1/2O2.

    PubMed

    Dupré, Nicolas; Cuisinier, Marine; Martin, Jean-Frederic; Guyomard, Dominique

    2014-07-21

    The present review reports the characterization and control of interfacial processes occurring on olivine LiFePO(4) and layered LiNi(1/2) Mn(1/2)O(2), standing here as model compounds, during storage and electrochemical cycling. The formation and evolution of the interphase created by decomposition of the electrolyte is investigated by using spectroscopic tools such as magic-angle-spinning nuclear magnetic resonance ((7)Li,(19)F and (31)P) and electron energy loss spectroscopy, in parallel to X-ray photoelectron spectroscopy, to quantitatively describe the interphase and unravel its architecture. The influence of the pristine surface chemistry of the active material is carefully examined. The importance of the chemical history of the surface of the electrode material before any electrochemical cycling and the strong correlation between interface phenomena, the formation/evolution of an interphase, and the electrochemical behavior appear clearly from the use of these combined characterization probes. This approach allows identifying interface aging and failure mechanisms. Different types of surface modifications are then investigated, such as intrinsic modifications upon aging in air or methods based on the use of additives in the electrolyte or carbon coatings on the surface of the active materials. In each case, the species detected on the surface of the materials during storage and cycling are correlated with the electrochemical performance of the modified positive electrodes.

  10. Influence of the temperature of electrode material on its disintegration under the action of an arc discharge in hydrogen

    NASA Technical Reports Server (NTRS)

    Bolotov, A. V.; Yukhimchuk, S. A.

    1985-01-01

    An analysis is made of the electrophysical processes occurring at the end surface of rod electrodes during constant and alternating arc discharge in hydrogen. Experiments are reported on the effect of surface temperature of tungsten electrodes on their erosion. The influence of activating additions of thorium oxide, the structure of the tungsten, and the gas surrounding the electrode on the specific thermal loading and the erosion of the electrodes is discussed.

  11. Evaluation of air permeability in layered unsaturated materials.

    PubMed

    Switzer, Christine; Kosson, David S

    2007-03-20

    Field estimation of air permeability is important in the design and operation of soil-vapor extraction systems. Previous models have examined airflow in homogenous soils, incorporating leakage through a low-permeability cap either as a correction to the airflow equation or as a boundary condition. The dual leakage model solution developed here improves upon the previous efforts by adding a leaky lower boundary condition, allowing for the examination of airflow in heterogeneous layered soils. The dual leakage model is applied to the evaluation of pump tests at a pilot soil-vapor extraction system at the Savannah River Site in South Carolina. A thick, low-permeability, stiff clay layer divides the stratigraphy at the site into two units for evaluation. A modified version of the previous model, using the water table as the impermeable lower boundary, is used to evaluate the permeability of the low-permeability stiff clay layer (3.2 x 10(-10) cm(2)) and permeable sand (7.2 x 10(-7) cm(2)) beneath it. The stiff clay permeability estimate is used in the evaluation of the shallow unit. Permeability estimates of the shallow sand (3.8 x 10(-7) cm(2)) and kaolin cap (1.5 x 10(-9)cm(2)) were obtained with the dual leakage model. The shallow unit was evaluated using the previous model for comparison. The effects of anisotropy were investigated with a series of model simulations based on the shallow unit solution. The anisotropy sensitivity analysis suggests that increased anisotropy ratio or decreased axial permeability has a significant impact on the velocity profile at the lower boundary, especially at high values of the anisotropy ratio. This result may increase estimates of SVE removal rates for contaminants located at the interface of the lower boundary, typical of chlorinated solvent contamination.

  12. Consideration of Thiol and Carboxylic Acid Chemisorption on Various Electrode Materials by Thermodynamic Calculation

    NASA Astrophysics Data System (ADS)

    Yagyu, Shinjiro; Yoshitake, Michiko; Chikyow, Toyohiro

    Thiols and carboxylic acids are important molecules for the anchor of Self-Assemble Monolayer (SAM) on metal surface in organic devices. In order to consider whether carboxylate or thiolate adsorbs on various metals, adsorption energies of methanthiolate and acetate on various metals were thermodynamically calculated using basic quantities of formation enthalpies of metal oxides (Hf(MxOy)) and metal sulfide (Hf(MxSy)). The calculations were carried out for the adsorption on clean, O adsorbed, and OH adsorbed surface. The results suggested that methanethiolate adsorbs on all clean metals, and on O and OH adsorbed metals except Ti and Al (the high Hf(MxOy) metals). On the other hand, acetate adsorbed on all O and OH covered metals, and the clean metals except Au, Ag and Pt (the low Hf(MxOy) metals). As the modification of electrodes using SAM is carried out under atmospheric and liquid conditions, it is considered that thiols prefer the adsorption on the low Hf(MxOy) metals to the high Hf(MxOy) metals, on the contrary, carboxylic acids prefer the adsorption on the high Hf(MxOy) metals to the low Hf(MxOy) metals.

  13. Combination of porous silica monolith and gold thin films for electrode material of supercapacitor

    NASA Astrophysics Data System (ADS)

    Pastre, A.; Cristini-Robbe, O.; Boé, A.; Raulin, K.; Branzea, D.; El Hamzaoui, H.; Kinowski, C.; Rolland, N.; Bernard, R.

    2015-12-01

    An all-solid electrical double layer supercapacitor was prepared, starting from a porous silica matrix coated with a gold thin-film. The metallization of the silica xerogel was performed by an original wet chemical process, based on the controlled growth of gold nanoparticles on two opposite faces of the silica monolith as a seed layer, followed by an electroless deposition of a continuous gold thin film. The thickness of the metallic thin film was assessed to be 700 nm. The silica plays two major roles: (1) it is used as a porous matrix for the gold electrode, creating a large specific surface area, and (2) it acts as a separator (non-metallized part of the silica). The silica monolith was soaked in a polyvinyl alcohol and phosphoric acid mixture which is used as polymer electrolyte. Capacitance effect was demonstrated by cyclic voltammetry experiments. The specific capacitance was found to be equal to 0.95 mF cm- 2 (9.5 F g-1). No major degradation occurs within more than 3000 cycles.

  14. A highly flexible electrochemical flow cell designed for the use of model electrode materials on non-conventional substrates

    NASA Astrophysics Data System (ADS)

    Temmel, S. E.; Tschupp, S. A.; Schmidt, T. J.

    2016-04-01

    We present a novel electrochemical flow cell based on a wall-jet configuration to carry out electrochemical investigations under controlled mass transport conditions. The described setup can be applied for investigations similar to those performed with a common rotating disc electrode setup but allows the use of non-conductive and square substrates. This setup thus opens the possibility for the characterization of a new range of materials on a broad range of substrates. Cyclic voltammograms were recorded to assess the cleanliness and good saturation of the cell with inert gas. The performance of the flow cell regarding hydrodynamic experiments was evaluated by probing the oxygen reduction reaction on differently prepared platinum catalysts, including Pt on non-conductive substrates. The high reproducibility of the limiting currents for these samples demonstrates the good functionality, adaptability, and flexibility of the cell.

  15. Solid oxide fuel cell with single material for electrodes and interconnect

    DOEpatents

    McPheeters, Charles C.; Nelson, Paul A.; Dees, Dennis W.

    1994-01-01

    A solid oxide fuel cell having a plurality of individual cells. A solid oxide fuel cell has an anode and a cathode with electrolyte disposed therebetween, and the anode, cathode and interconnect elements are comprised of substantially one material.

  16. Optimized spherical manganese oxide-ferroferric oxide-tin oxide ternary composites as advanced electrode materials for supercapacitors

    NASA Astrophysics Data System (ADS)

    Zhu, Jian; Tang, Shaochun; Vongehr, Sascha; Xie, Hao; Meng, Xiangkang

    2015-09-01

    Inexpensive MnO2 is a promising material for supercapacitors (SCs), but its application is limited by poor electrical conductivity and low specific surface area. We design and fabricate hierarchical MnO2-based ternary composite nanostructures showing superior electrochemical performance via doping with electrochemically active Fe3O4 in the interior and electrically conductive SnO2 nanoparticles in the surface layer. Optimization composition results in a MnO2-Fe3O4-SnO2 composite electrode material with 5.9 wt.% Fe3O4 and 5.3 wt.% SnO2, leading to a high specific areal capacitance of 1.12 F cm-2 at a scan rate of 5 mV s-1. This is two to three times the values for MnO2-based binary nanostructures at the same scan rate. The low amount of SnO2 almost doubles the capacitance of porous MnO2-Fe3O4 (before SnO2 addition), which is attributed to an improved conductivity and remaining porosity. In addition, the optimal ternary composite has a good rate capability and an excellent cycling performance with stable capacitance retention of ˜90% after 5000 charge/discharge cycles at 7.5 mA cm-2. All-solid-state SCs are assembled with such electrodes using polyvinyl alcohol/Na2SO4 electrolyte. An integrated device made by connecting two identical SCs in series can power a light-emitting diode indicator for more than 10 min.

  17. Optimized spherical manganese oxide-ferroferric oxide-tin oxide ternary composites as advanced electrode materials for supercapacitors.

    PubMed

    Zhu, Jian; Tang, Shaochun; Vongehr, Sascha; Xie, Hao; Meng, Xiangkang

    2015-09-18

    Inexpensive MnO2 is a promising material for supercapacitors (SCs), but its application is limited by poor electrical conductivity and low specific surface area. We design and fabricate hierarchical MnO2-based ternary composite nanostructures showing superior electrochemical performance via doping with electrochemically active Fe3O4 in the interior and electrically conductive SnO2 nanoparticles in the surface layer. Optimization composition results in a MnO2-Fe3O4-SnO2 composite electrode material with 5.9 wt.% Fe3O4 and 5.3 wt.% SnO2, leading to a high specific areal capacitance of 1.12 F cm(-2) at a scan rate of 5 mV s(-1). This is two to three times the values for MnO2-based binary nanostructures at the same scan rate. The low amount of SnO2 almost doubles the capacitance of porous MnO2-Fe3O4 (before SnO2 addition), which is attributed to an improved conductivity and remaining porosity. In addition, the optimal ternary composite has a good rate capability and an excellent cycling performance with stable capacitance retention of ~90% after 5000 charge/discharge cycles at 7.5 mA cm(-2). All-solid-state SCs are assembled with such electrodes using polyvinyl alcohol/Na2SO4 electrolyte. An integrated device made by connecting two identical SCs in series can power a light-emitting diode indicator for more than 10 min. PMID:26314271

  18. Monitor of the concentration of particles of dense radioactive materials in a stream of air

    DOEpatents

    Yule, Thomas J.

    1979-01-01

    A monitor of the concentration of particles of radioactive materials such as plutonium oxide in diameters as small as 1/2 micron includes in combination a first stage comprising a plurality of virtual impactors, a second stage comprising a further plurality of virtual impactors, a collector for concentrating particulate material, a radiation detector disposed near the collector to respond to radiation from collected material and means for moving a stream of air, possibly containing particulate contaminants, through the apparatus.

  19. Nano-sized structured layered positive electrode materials to enable high energy density and high rate capability lithium batteries

    DOEpatents

    Deng, Haixia; Belharouak, Ilias; Amine, Khalil

    2012-10-02

    Nano-sized structured dense and spherical layered positive active materials provide high energy density and high rate capability electrodes in lithium-ion batteries. Such materials are spherical second particles made from agglomerated primary particles that are Li.sub.1+.alpha.(Ni.sub.xCo.sub.yMn.sub.z).sub.1-tM.sub.tO.sub.2-dR.sub.d- , where M is selected from can be Al, Mg, Fe, Cu, Zn, Cr, Ag, Ca, Na, K, In, Ga, Ge, V, Mo, Nb, Si, Ti, Zr, or a mixture of any two or more thereof, R is selected from F, Cl, Br, I, H, S, N, or a mixture of any two or more thereof, and 0.ltoreq..alpha..ltoreq.0.50; 0materials and their use in electrochemical devices are also described.

  20. A nickel hydroxide-coated 3D porous graphene hollow sphere framework as a high performance electrode material for supercapacitors.

    PubMed

    Zhang, Fengqiao; Zhu, Dong; Chen, Xi'an; Xu, Xin; Yang, Zhi; Zou, Chao; Yang, Keqin; Huang, Shaoming

    2014-03-01

    A three-dimensional (3D) porous graphene hollow sphere (PGHS) framework has been fabricated via a hard template method and used to anchor α-Ni(OH)2 nanoparticles with the size of about 4 nm through electrochemical deposition. It is found that a 3D PGHS framework can improve the capacitive performance of Ni(OH)2 effectively. In hybrid materials, α-Ni(OH)2 achieves the high specific capacitance of 2815 F g(-1) at a scan rate of 5 mV s(-1) and 1950 F g(-1) even at 200 mV s(-1) with a capacitance retention of about 70%, indicating that the α-Ni(OH)2-coated 3D PGHS framework exhibits high rate capability. The excellent performance of such hybrid material is believed to be due to the smaller size of Ni(OH)2 nanoparticles and the PGHS framework with large specific surface area promoting efficient electron transport and facilitating the electrolyte ions migration. These impressive results suggest that the composite is a promising electrode material for an efficient supercapacitor.

  1. Chemical and structural stability of lithium-ion battery electrode materials under electron beam.

    PubMed

    Lin, Feng; Markus, Isaac M; Doeff, Marca M; Xin, Huolin L

    2014-01-01

    The investigation of chemical and structural dynamics in battery materials is essential to elucidation of structure-property relationships for rational design of advanced battery materials. Spatially resolved techniques, such as scanning/transmission electron microscopy (S/TEM), are widely applied to address this challenge. However, battery materials are susceptible to electron beam damage, complicating the data interpretation. In this study, we demonstrate that, under electron beam irradiation, the surface and bulk of battery materials undergo chemical and structural evolution equivalent to that observed during charge-discharge cycling. In a lithiated NiO nanosheet, a Li2CO3-containing surface reaction layer (SRL) was gradually decomposed during electron energy loss spectroscopy (EELS) acquisition. For cycled LiNi(0.4)Mn(0.4)Co(0.18)Ti(0.02)O2 particles, repeated electron beam irradiation induced a phase transition from an layered structure to an rock-salt structure, which is attributed to the stoichiometric lithium and oxygen removal from 3a and 6c sites, respectively. Nevertheless, it is still feasible to preserve pristine chemical environments by minimizing electron beam damage, for example, using fast electron imaging and spectroscopy. Finally, the present study provides examples of electron beam damage on lithium-ion battery materials and suggests that special attention is necessary to prevent misinterpretation of experimental results.

  2. Chemical and Structural Stability of Lithium-Ion Battery Electrode Materials under Electron Beam

    PubMed Central

    Lin, Feng; Markus, Isaac M.; Doeff, Marca M.; Xin, Huolin L.

    2014-01-01

    The investigation of chemical and structural dynamics in battery materials is essential to elucidation of structure-property relationships for rational design of advanced battery materials. Spatially resolved techniques, such as scanning/transmission electron microscopy (S/TEM), are widely applied to address this challenge. However, battery materials are susceptible to electron beam damage, complicating the data interpretation. In this study, we demonstrate that, under electron beam irradiation, the surface and bulk of battery materials undergo chemical and structural evolution equivalent to that observed during charge-discharge cycling. In a lithiated NiO nanosheet, a Li2CO3-containing surface reaction layer (SRL) was gradually decomposed during electron energy loss spectroscopy (EELS) acquisition. For cycled LiNi0.4Mn0.4Co0.18Ti0.02O2 particles, repeated electron beam irradiation induced a phase transition from an layered structure to an rock-salt structure, which is attributed to the stoichiometric lithium and oxygen removal from 3a and 6c sites, respectively. Nevertheless, it is still feasible to preserve pristine chemical environments by minimizing electron beam damage, for example, using fast electron imaging and spectroscopy. Finally, the present study provides examples of electron beam damage on lithium-ion battery materials and suggests that special attention is necessary to prevent misinterpretation of experimental results. PMID:25027190

  3. Facile Green Synthesis of BCN Nanosheets as High-Performance Electrode Material for Electrochemical Energy Storage.

    PubMed

    Karbhal, Indrapal; Devarapalli, Rami Reddy; Debgupta, Joyashish; Pillai, Vijayamohanan K; Ajayan, Pulickel M; Shelke, Manjusha V

    2016-05-17

    Two-dimensional hexagonal boron carbon nitride (BCN) nanosheets (NSs) were synthesized by new approach in which a mixture of glucose and an adduct of boric acid (H3 BO3 ) and urea (NH2 CONH2 ) is heated at 900 °C. The method is green, scalable and gives a high yield of BCN NSs with average size of about 1 μm and thickness of about 13 nm. Structural characterization of the as-synthesized material was carried out by several techniques, and its energy-storage properties were evaluated electrochemically. The material showed excellent capacitive behaviour with a specific capacitance as high as 244 F g(-1) at a current density of 1 A g(-1) . The material retains up to 96 % of its initial capacity after 3000 cycles at a current density of 5 A g(-1) . PMID:27072914

  4. FTIR features of lithium-iron phosphates as electrode materials for rechargeable lithium batteries.

    PubMed

    Ait Salah, A; Jozwiak, P; Zaghib, K; Garbarczyk, J; Gendron, F; Mauger, A; Julien, C M

    2006-12-01

    The essential structural features of lithium-metal phosphates (LMP) have been studied using FTIR spectroscopy which is a sensitive tool to probe the local environment in the solid materials. Various LMP materials where M is iron have been investigated including phospho-olivine LiFePO(4), diphosphate LiFeP(2)O(7), Nasicon-type phosphate Li(3)Fe(2)(PO(4))(3) and dihydrate FePO(4).2H(2)O. Vitreous and amorphous materials are also considered. Analysis of internal and external modes of vibration allows to distinguish between the different phases and the type of cationic environment in the framework. Results corroborate the contribution of the main factors which are responsible for the complexity of the spectra, i.e. departure from ideal symmetry, interactions between polyhedra, bridging atoms and lattice distortion.

  5. Facile Green Synthesis of BCN Nanosheets as High-Performance Electrode Material for Electrochemical Energy Storage.

    PubMed

    Karbhal, Indrapal; Devarapalli, Rami Reddy; Debgupta, Joyashish; Pillai, Vijayamohanan K; Ajayan, Pulickel M; Shelke, Manjusha V

    2016-05-17

    Two-dimensional hexagonal boron carbon nitride (BCN) nanosheets (NSs) were synthesized by new approach in which a mixture of glucose and an adduct of boric acid (H3 BO3 ) and urea (NH2 CONH2 ) is heated at 900 °C. The method is green, scalable and gives a high yield of BCN NSs with average size of about 1 μm and thickness of about 13 nm. Structural characterization of the as-synthesized material was carried out by several techniques, and its energy-storage properties were evaluated electrochemically. The material showed excellent capacitive behaviour with a specific capacitance as high as 244 F g(-1) at a current density of 1 A g(-1) . The material retains up to 96 % of its initial capacity after 3000 cycles at a current density of 5 A g(-1) .

  6. Few layered vanadyl phosphate nano sheets-MWCNT hybrid as an electrode material for supercapacitor application

    NASA Astrophysics Data System (ADS)

    Dutta, Shibsankar; De, Sukanta

    2016-05-01

    It have been already seen that 2-dimensional nano materials are the suitable choice for the supercapacitor application due to their large specific surface area, electrochemical active sites, micromechanical flexibility, expedite ion migration channel properties. Free standing hybrid films of functionalized MWCNT (- COOH group) and α-Vanadyl phosphates (VOPO42H2O) are prepared by vacuum filtering. The surface morphology and microstructure of the samples are studied by transmission electron microscope, field emission scanning electron microscope, XRD, Electrochemical properties of hybrid films have been investigated systematically in 1M Na2SO4 aqueous electrolyte. The hybrid material exhibits a high specific capacitance 236 F/g with high energy density of 65.6 Wh/Kg and a power density of 1476 W/Kg.

  7. Preparation of energy storage material derived from a used cigarette filter for a supercapacitor electrode

    NASA Astrophysics Data System (ADS)

    Lee, Minzae; Kim, Gil-Pyo; Song, Hyeon Don; Park, Soomin; Yi, Jongheop

    2014-08-01

    We report on a one-step method for preparing nitrogen doped (N-doped) meso-/microporous hybrid carbon material (NCF) via the heat treatment of used cigarette filters under a nitrogen-containing atmosphere. The used cigarette filter, which is mostly composed of cellulose acetate fibers, can be transformed into a porous carbon material that contains both the mesopores and micropores spontaneously. The unique self-developed pore structure allowed a favorable pathway for electrolyte permeation and contact probability, resulting in the extended rate capability for the supercapacitor. The NCF exhibited a better rate capability and higher specific capacitance (153.8 F g-1) compared to that of conventional activated carbon (125.0 F g-1) at 1 A g-1. These findings indicate that the synergistic combination of well-developed meso-/micropores, an enlarged surface area and pseudocapacitive behavior leads to the desired supercapacitive performance. The prepared carbon material is capable of reproducing its electrochemical performance during the 6000 cycles required for charge and discharge measurements.

  8. Synthesis and Characterization of Novel Chromium-Free Nickel Alloy Electrode Materials

    NASA Astrophysics Data System (ADS)

    Nataraj, J. R.; Krishna, M.; Murthy, H. N. Narasimha; Prasad, C. S.; Bhanukiran, V. T.; Sharma, S. C.

    2013-07-01

    The synthesis of two Cr-free nickel-based alloys designated as 1S with 6.5 pct Mn and 2H without Mn of compositions varying between 40 to 43.5Ni, 20Mo, 22 to 25Fe, 10Cu, 6.5 to 0Mn, 1Ti, and 0.5Al (wt pct) as filler materials for TIG welding application was performed. New filler materials were developed to reduce carcinogenic hexavalent chromium (Cr6+) fumes generated during the welding of 300 series austenitic stainless steel. The Cr-free nickel alloys were characterized for microstructure and mechanical properties. The developed alloys showed good microstructure stability in as-cast and solution-treated conditions. A material properties simulation software JMatPro predicted that 2H alloy has 2 wt pct more γ (solid solution) phase than in 1S but has 2.2 wt pct less γ' (strengthening precipitates) phase than in 1S alloy. The tensile strength of 1S alloy was about 2.2 pct more than 2H. The solution treatment of both alloys decreased the hardness, tensile and yield strengths by about 21 pct but ductility improved by about 17 pct. Fracture studies of both alloys showed the ductile mode of failure.

  9. A difference in using atomic layer deposition or physical vapour deposition TiN as electrode material in metal-insulator-metal and metal-insulator-silicon capacitors.

    PubMed

    Groenland, A W; Wolters, R A M; Kovalgin, A Y; Schmitz, J

    2011-09-01

    In this work, metal-insulator-metal (MIM) and metal-insulator-silicon (MIS) capacitors are studied using titanium nitride (TiN) as the electrode material. The effect of structural defects on the electrical properties on MIS and MIM capacitors is studied for various electrode configurations. In the MIM capacitors the bottom electrode is a patterned 100 nm TiN layer (called BE type 1), deposited via sputtering, while MIS capacitors have a flat bottom electrode (called BE type 2-silicon substrate). A high quality 50-100 nm thick SiO2 layer, made by inductively-coupled plasma CVD at 150 degrees C, is deposited as a dielectric on top of both types of bottom electrodes. BE type 1 (MIM) capacitors have a varying from low to high concentration of structural defects in the SiO2 layer. BE type 2 (MIS) capacitors have a low concentration of structural defects and are used as a reference. Two sets of each capacitor design are fabricated with the TiN top electrode deposited either via physical vapour deposition (PVD, i.e., sputtering) or atomic layer deposition (ALD). The MIM and MIS capacitors are electrically characterized in terms of the leakage current at an electric field of 0.1 MV/cm (I leak) and for different structural defect concentrations. It is shown that the structural defects only show up in the electrical characteristics of BE type 1 capacitors with an ALD TiN-based top electrode. This is due to the excellent step coverage of the ALD process. This work clearly demonstrates the sensitivity to process-induced structural defects, when ALD is used as a step in process integration of conductors on insulation materials.

  10. Methods for and products of processing nanostructure nitride, carbonitride and oxycarbonitride electrode power materials by utilizing sol gel technology for supercapacitor applications

    DOEpatents

    Huang, Yuhong; Wei, Oiang; Chu, Chung-tse; Zheng, Haixing

    2001-01-01

    Metal nitride, carbonitride, and oxycarbonitride powder with high surface area (up to 150 m.sup.2 /g) is prepared by using sol-gel process. The metal organic precursor, alkoxides or amides, is synthesized firstly. The metal organic precursor is modified by using unhydrolyzable organic ligands or templates. A wet gel is formed then by hydrolysis and condensation process. The solvent in the wet gel is then be removed supercritically to form porous amorphous hydroxide. This porous hydroxide materials is sintered to 725.degree. C. under the ammonia flow and porous nitride powder is formed. The other way to obtain high surface area nitride, carbonitride, and oxycarbonitride powder is to pyrolyze polymerized templated metal amides aerogel in an inert atmosphere. The electrochemical capacitors are prepared by using sol-gel prepared nitride, carbonitride, and oxycarbonitride powder. Two methods are used to assemble the capacitors. Electrode is formed either by pressing the mixture of nitride powder and binder to a foil, or by depositing electrode coating onto metal current collector. The binder or coating is converted into a continuous network of electrode material after thermal treatment to provide enhanced energy and power density. Liquid electrolyte is soaked into porous electrode. The electrochemical capacitor assembly further has a porous separator layer between two electrodes/electrolyte and forming a unit cell.

  11. Advanced cathode materials for polymer electrolyte fuel cells based on pt/ metal oxides: from model electrodes to catalyst systems.

    PubMed

    Fabbri, Emiliana; Pătru, Alexandra; Rabis, Annett; Kötz, Rüdiger; Schmidt, Thomas J

    2014-01-01

    The development of stable catalyst systems for application at the cathode side of polymer electrolyte fuel cells (PEFCs) requires the substitution of the state-of-the-art carbon supports with materials showing high corrosion resistance in a strongly oxidizing environment. Metal oxides in their highest oxidation state can represent viable support materials for the next generation PEFC cathodes. In the present work a multilevel approach has been adopted to investigate the kinetics and the activity of Pt nanoparticles supported on SnO2-based metal oxides. Particularly, model electrodes made of SnO2 thin films supporting Pt nanoparticles, and porous catalyst systems made of Pt nanoparticles supported on Sb-doped SnO2 high surface area powders have been investigated. The present results indicate that SnO2-based supports do not modify the oxygen reduction reaction mechanism on the Pt nanoparticle surface, but rather lead to catalysts with enhanced specific activity compared to Pt/carbon systems. Different reasons for the enhancement in the specific activity are considered and discussed.

  12. RSM model to evaluate material removal rate in EDM of Ti-5Al-2.5Sn using graphite electrode

    NASA Astrophysics Data System (ADS)

    Ashikur Rahman Khan, Md; Rahman, M. M.; Kadirgama, K.; Ismail, A. R.

    2012-09-01

    The usage of electrical discharge machining (EDM) is increasing gradually owing to its capability to cut precisely, geometrically complex material regardless hardness. Many process parameters greatly affect the EDM performance and complicated mechanism of the process result the lag of established theory. Hence, it becomes important to select the proper parameter set for different machining stages in order to promote efficiency. In view of these barriers, it is attempted to establish a model which can accurately predict the material removal rate (MRR) of titanium alloy by correlating the process parameter. Effect of the parameters on MRR is investigated as well. Experiment is conducted utilizing the graphite electrode maintaining negative polarity. Analysis and modelling is carried out based on design of experiment as well as response surface methodology. The agreeable accuracy is obtained and thus the model can become a precise tool setting the EDM process cost effective and efficient. Moreover, high ampere, short pulse-off time and low servo-voltage combined with about 250 μs pulse-on time generate the highest MRR.

  13. Attenuation of intense sinusoidal waves in air-saturated, bulk porous materials

    NASA Technical Reports Server (NTRS)

    Kuntz, Herbert L.; Blackstock, David T.

    1987-01-01

    As intense, initially sinusoidal waves propagate in fluids, shocks form and excess attenuation of the wave occurs. Data are presented indicating that shock formation is not necessary for the occurrence of excess attenuation in nonlinear, lossy media, i.e., air-saturated, porous materials. An empirical equation is used to describe the excess attenuation of intense sinusoids in porous materials. The acoustic nonlinearity of and the excess attenuation in porous materials may be predicted directly from dc flow resistivity data. An empirical relationship is used to relate an acoustic nonlinearity parameter to the fundamental frequency and relative dc nonlinearity of two structurally different materials.

  14. Measurement of the resistivity of porous materials with an alternating air-flow method.

    PubMed

    Dragonetti, Raffaele; Ianniello, Carmine; Romano, Rosario A

    2011-02-01

    Air-flow resistivity is a main parameter governing the acoustic behavior of porous materials for sound absorption. The international standard ISO 9053 specifies two different methods to measure the air-flow resistivity, namely a steady-state air-flow method and an alternating air-flow method. The latter is realized by the measurement of the sound pressure at 2 Hz in a small rigid volume closed partially by the test sample. This cavity is excited with a known volume-velocity sound source implemented often with a motor-driven piston oscillating with prescribed area and displacement magnitude. Measurements at 2 Hz require special instrumentation and care. The authors suggest an alternating air-flow method based on the ratio of sound pressures measured at frequencies higher than 2 Hz inside two cavities coupled through a conventional loudspeaker. The basic method showed that the imaginary part of the sound pressure ratio is useful for the evaluation of the air-flow resistance. Criteria are discussed about the choice of a frequency range suitable to perform simplified calculations with respect to the basic method. These criteria depend on the sample thickness, its nonacoustic parameters, and the measurement apparatus as well. The proposed measurement method was tested successfully with various types of acoustic materials.

  15. Smart plastic antibody material (SPAM) tailored on disposable screen printed electrodes for protein recognition: application to myoglobin detection.

    PubMed

    Moreira, Felismina T C; Sharma, Sanjiv; Dutra, Rosa A F; Noronha, João P C; Cass, Anthony E G; Sales, M Goreti F

    2013-07-15

    This work introduces two major changes to the conventional protocol for designing plastic antibodies: (i) the imprinted sites were created with charged monomers while the surrounding environment was tailored using neutral material; and (ii) the protein was removed from its imprinted site by means of a protease, aiming at preserving the polymeric network of the plastic antibody. To our knowledge, these approaches were never presented before and the resulting material was named here as smart plastic antibody material (SPAM). As proof of concept, SPAM was tailored on top of disposable gold-screen printed electrodes (Au-SPE), following a bottom-up approach, for targeting myoglobin (Myo) in a point-of-care context. The existence of imprinted sites was checked by comparing a SPAM modified surface to a negative control, consisting of similar material where the template was omitted from the procedure and called non-imprinted materials (NIMs). All stages of the creation of the SPAM and NIM on the Au layer were followed by both electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). AFM imaging was also performed to characterize the topography of the surface. There are two major reasons supporting the fact that plastic antibodies were effectively designed by the above approach: (i) they were visualized for the first time by AFM, being present only in the SPAM network; and (ii) only the SPAM material was able to rebind to the target protein and produce a linear electrical response against EIS and square wave voltammetry (SWV) assays, with NIMs showing a similar-to-random behavior. The SPAM/Au-SPE devices displayed linear responses to Myo in EIS and SWV assays down to 3.5 μg/mL and 0.58 μg/mL, respectively, with detection limits of 1.5 and 0.28 μg/mL. SPAM materials also showed negligible interference from troponin T (TnT), bovine serum albumin (BSA) and urea under SWV assays, showing promising results for point-of-care applications when applied to spiked

  16. Use of cooling air heat exchangers as replacements for hot section strategic materials

    NASA Technical Reports Server (NTRS)

    Gauntner, J. W.

    1983-01-01

    Because of financial and political constraints, strategic aerospace materials required for the hot section of future engines might be in short supply. As an alternative to these strategic materials, this study examines the use of a cooling air heat exchanger in combination with less advanced hot section materials. Cycle calculations are presented for future turbofan systems with overall pressure ratios to 65, bypass ratios near 13, and combustor exit temperatures to 3260 R. These calculations quantify the effect on TSFC of using a decreased materials technology in a turbofan system. The calculations show that the cooling air heat exchanger enables the feasibility of these engines. Previously announced in STAR as N83-34946

  17. Material Development and Processing of Multiscale Structured Ceramics for SOFC-Electrodes

    NASA Astrophysics Data System (ADS)

    Neukam, M.; Pannerselvam, M.; Willert-Porada, M.

    2008-02-01

    NiO-ZrO2-cermets are used as anode material in Solid Oxide Fuel Cells. A sub-structured cermet consisting aligned lamella of NiO and 8Y-ZrO2 is obtained by melt processing of a eutectic powder mixture. Direct co-firing of such cermet powders with the ceramic electrolyte layer requires sintering temperatures above 1600 °C and leads to redistribution of NiO. Sintering with AlN as reactive component for in-situ formation of cubic ZrxOyNz, promotes joining of the sub-structured anode material with the solid electrolyte via the ionic conductive 8Y-ZrO2-grains at 1400-1550 °C. By decomposition of the Zr-oxynitride upon cooling, new porosity and the desired connectivity between the anode and the solid electrolyte is formed. A graded composite is obtained at an interface, which consists of e.g., ZrO2, Zr7O9.5N3, β-ZrAlON, NiAl2O4 and Ni, depending upon the sintering temperature.

  18. Evaluation of materials for sliding at 600F-1800F in air.

    NASA Technical Reports Server (NTRS)

    Finkin, E. F.; Calabrese, S. J.; Peterson, M. B.

    1972-01-01

    Oscillating sliding tests were conducted in air under the following operating conditions: 500 psi, 600 F; 500 psi, 1200 F; 500 psi, 1800 F; 1500 psi, 1800 F; 3000 psi, 1800 F. Sixteen materials combinations were tested including ceramics, alloys and eutectics, cermets, and combinations of these. Friction, wear and surface damage (including surface roughening) were studied. The most outstanding materials combination was found to be nickel-molybdenum-bonded titanium carbide cermet sliding against dense magnesia stabilized ZrO2.

  19. How to avoid indoor air quality (IAQ) claims through better design and materials selection

    SciTech Connect

    Halliwell, J.L.

    1994-12-31

    Over the past 5 years, there has been an explosion of complaints, claims and subsequent litigation resulting from unacceptable indoor air quality (IAQ) in buildings. Unlike asbestos claims that were directed primarily against manufacturers, IAQ litigation is often leveled against building owners, their architects, engineers, and contractors by building occupants. The problem is getting worse. EPA, citing that the air inside buildings is often as much as 100 times more polluted than the air outside, now considers indoor air pollution as one of the most severe environmental risks to Human Health in the US. The World Health Organization (WHO) estimates that approximately 30% of all new or renovated buildings have an indoor air quality problem. In the past, the importance of indoor air quality was overshadowed by concerns with the outdoor environment. The quality of the indoor air is now a major health and legal issue for building owners and their agents. This presentation will offer a brief overview of Halliwell Engineering Associates` 40 years of HVAC experience in analyzing and resolving IAQ problems in buildings. It will present some of the typical causes of IAQ complaints, common mistakes that designers make and how to avoid them. It will also present an overview of how construction materials often contribute to the problem by generating a large number of pollutants themselves, and what building owners can do to minimize that problem. Finally, they will provide specifics on how to ensure that the newly constructed space will not result in future IAQ complaints or claims.

  20. Work function determination of promising electrode materials for thermionic energy converters

    NASA Technical Reports Server (NTRS)

    Jacobson, D.; Storms, E.; Skaggs, B.; Kouts, T.; Jaskie, J.; Manda, M.

    1976-01-01

    The work function determinations of candidate materials for low temperature (1400 K) thermionics through vacuum emission tests are discussed. Two systems, a vacuum emission test vehicle and a thermionic emission microscope are used for emission measurements. Some nickel and cobalt based super alloys were preliminarily examined. High temperature physical properties and corrosion behavior of some super alloy candidates are presented. The corrosion behavior of sodium is of particular interest since topping cycles might use sodium heat transfer loops. A Marchuk tube was designed for plasma discharge studies with the carbide and possibly some super alloy samples. A series of metal carbides and other alloys were fabricated and tested in a special high temperature mass spectrometer. This information coupled with work function determinations was evaluated in an attempt to learn how electron bonding occurs in transition alloys.

  1. Moving Graphitic Carbon Nitride from Electrocatalysis and Photocatalysis to a Potential Electrode Material for Photoelectric Devices.

    PubMed

    Xu, Jingsan; Antonietti, Markus; Shalom, Menny

    2016-09-20

    Carbon nitride (g-CN) has attracted significant interest in the last years as a robust, low-cost alternative to metal-based materials in different fields due to its low price, environmentally benign character, simple synthesis and tunable properties. In particular, g-CN demonstrates promising activity in energy-related applications such as photo and heterogeneous catalysis, batteries and electrolysis. However, while g-CN is already well-established as a photocatalyst, its utilization in (opto)electronic devices is still at an early stage. This Focus Review concentrates on the utilization of g-CN in solar and photoelectrochemical cells, electrolyzers and light emitting diode alongside the recap of new synthetic approaches. This review is expected to provide useful insights into the design and fabrication of g-CN based photoelectronic devices as well as g-CN working principles, including the main challenges toward its integration in optoelectronic devices. PMID:27558641

  2. Moving Graphitic Carbon Nitride from Electrocatalysis and Photocatalysis to a Potential Electrode Material for Photoelectric Devices.

    PubMed

    Xu, Jingsan; Antonietti, Markus; Shalom, Menny

    2016-09-20

    Carbon nitride (g-CN) has attracted significant interest in the last years as a robust, low-cost alternative to metal-based materials in different fields due to its low price, environmentally benign character, simple synthesis and tunable properties. In particular, g-CN demonstrates promising activity in energy-related applications such as photo and heterogeneous catalysis, batteries and electrolysis. However, while g-CN is already well-established as a photocatalyst, its utilization in (opto)electronic devices is still at an early stage. This Focus Review concentrates on the utilization of g-CN in solar and photoelectrochemical cells, electrolyzers and light emitting diode alongside the recap of new synthetic approaches. This review is expected to provide useful insights into the design and fabrication of g-CN based photoelectronic devices as well as g-CN working principles, including the main challenges toward its integration in optoelectronic devices.

  3. Superior supercapacitor electrode material from hydrazine hydrate modified porous polyacrylonitrile fiber

    NASA Astrophysics Data System (ADS)

    Li, Ying; Lu, Chunxiang; Wang, Junzhong; Yan, Hua; Zhang, Shouchun

    2016-03-01

    A hierarchical porous carbon fiber with high nitrogen doping was fabricated for high-performance supercapacitor. For the purpose of high nitrogen retention, the porous polyacrylonitrile fiber was treated by hydrazine hydrate, and then underwent pre-oxidation, carbonization, and activation in sequence. The resulted material exhibited high nitrogen content of 7.82 at.%, large specific surface area of 1963.3m2 g‑1, total pore volume of 1.523cm3 g‑1, and the pores with size range of 1-4nm were account for 49.1%. Due to these features, the high reversible capacitance of 415F g‑1 and the good performance in heavy load discharge were obtained. In addition, the amazing cyclability was observed after 10,000 circles without capacitance fading.

  4. Investigation of a novel polymer foam material for air coupled ultrasonic transducer applications

    NASA Astrophysics Data System (ADS)

    Satyanarayan, L.; Weide, J. M. Vander; Declercq, N. F.; Berthelot, Y.

    This experimental study aims at investigating the use of porous polymer foam piezoelectrets as a potential transducer material for air coupled ultrasonic applications. When a voltage is applied, these materials exhibit a phenomenon similar to the inverse piezoelectric effect. The defining features of the piezo-like polymer foam are small, elliptically shaped and electrically polarized voids located inside the polymers. The sensitivity is related to the effective piezoelectric coupling coefficient d33 which is much higher than in traditional piezoelectric materials. The d33 values of the cellular polypropylene foams were estimated using a laser vibrometer at different input voltages for a continuous wave excitation. It was observed that the effective d33 coefficient strongly depends on the volume fraction of electrically charged voids in the material as the material compliance decreases with increased material voids. The change in acoustic impedance across the surface of the sample was measured with a high-resolution ultrasonic scanning system. Finally, these foams were used as prototype transducers for the transmit-receive mode in air; practical limitations imposed by acoustic attenuation in air were assessed.

  5. 10 CFR 835.209 - Concentrations of radioactive material in air.

    Code of Federal Regulations, 2012 CFR

    2012-01-01

    ... concentration (DAC) values given in appendices A and C of this part shall be used in the control of occupational... 10 Energy 4 2012-01-01 2012-01-01 false Concentrations of radioactive material in air. 835.209 Section 835.209 Energy DEPARTMENT OF ENERGY OCCUPATIONAL RADIATION PROTECTION Standards for Internal...

  6. 10 CFR 835.209 - Concentrations of radioactive material in air.

    Code of Federal Regulations, 2011 CFR

    2011-01-01

    ... concentration (DAC) values given in appendices A and C of this part shall be used in the control of occupational... 10 Energy 4 2011-01-01 2011-01-01 false Concentrations of radioactive material in air. 835.209 Section 835.209 Energy DEPARTMENT OF ENERGY OCCUPATIONAL RADIATION PROTECTION Standards for Internal...

  7. 10 CFR 835.209 - Concentrations of radioactive material in air.

    Code of Federal Regulations, 2013 CFR

    2013-01-01

    ... concentration (DAC) values given in appendices A and C of this part shall be used in the control of occupational... 10 Energy 4 2013-01-01 2013-01-01 false Concentrations of radioactive material in air. 835.209 Section 835.209 Energy DEPARTMENT OF ENERGY OCCUPATIONAL RADIATION PROTECTION Standards for Internal...

  8. 10 CFR 835.209 - Concentrations of radioactive material in air.

    Code of Federal Regulations, 2014 CFR

    2014-01-01

    ... concentration (DAC) values given in appendices A and C of this part shall be used in the control of occupational... 10 Energy 4 2014-01-01 2014-01-01 false Concentrations of radioactive material in air. 835.209 Section 835.209 Energy DEPARTMENT OF ENERGY OCCUPATIONAL RADIATION PROTECTION Standards for Internal...

  9. Iron aluminides and nickel aluminides as materials for chemical air separation

    DOEpatents

    Kang, D.

    1991-01-29

    The present invention is directed to a chemical air separation process using a molten salt solution of alkali metal nitrate and nitrite wherein the materials of construction of the containment for the process are chosen from intermetallic alloys of nickel and/or iron aluminide wherein the aluminum content is 28 atomic percent or greater to impart enhanced corrosion resistance.

  10. Iron aluminides and nickel aluminides as materials for chemical air separation

    DOEpatents

    Kang, Doohee

    1991-01-01

    The present invention is directed to a chemical air separation process using a molten salt solution of alkali metal nitrate and nitrite wherein the materials of construction of the containment for the process are chosen from intermetallic alloys of nickel and/or iron aluminide wherein the aluminum content is 28 atomic percent or greater to impart enhanced corrosion resistance.

  11. Effect of bedding material on air quality of bedded manure packs in livestock facilities

    Technology Transfer Automated Retrieval System (TEKTRAN)

    Bedding materials may affect air quality in livestock facilities. The objective of this study was to compare headspace concentrations of odorous volatile organic compounds (VOC), total reduce sulfur (TRS), CO2, CH4, and N2O when corn stover, bean stover, wheat straw, switch grass, pine wood chips, p...

  12. 5 CFR 842.405 - Air traffic controllers, firefighters, law enforcement officers, and nuclear materials couriers.

    Code of Federal Regulations, 2010 CFR

    2010-01-01

    ..., law enforcement officers, and nuclear materials couriers. 842.405 Section 842.405 Administrative Personnel OFFICE OF PERSONNEL MANAGEMENT (CONTINUED) CIVIL SERVICE REGULATIONS (CONTINUED) FEDERAL EMPLOYEES RETIREMENT SYSTEM-BASIC ANNUITY Computations § 842.405 Air traffic controllers, firefighters, law...

  13. Refrigeration and Air Conditioning Equipment, 11-9. Military Curriculum Materials for Vocational and Technical Education.

    ERIC Educational Resources Information Center

    Ohio State Univ., Columbus. National Center for Research in Vocational Education.

    This military-developed text consists of three blocks of instructional materials for use by those studying to become refrigeration and air conditioning specialists. Covered in the individual course blocks are the following topics: refrigeration and trouble analysis, thermodynamics, and principles of refrigeration; major components and domestic and…

  14. Modified by air plasma polymer tack membranes as drainage material for antiglaucomatous operations

    NASA Astrophysics Data System (ADS)

    Ryazantseva, T. V.; Kravets, L. I.; Elinson, V. M.

    2014-06-01

    The morphological and clinical studies of poly(ethylene terephthalate) track membranes modified by air plasma as drainage materials for antiglaucomatous operations were performed. It was demonstrated their compatibility with eye tissues. Moreover, it was shown that a new drainage has a good lasting hypotensive effect and can be used as operation for refractory glaucoma surgery.

  15. A hierarchical porous electrode using a micron-sized honeycomb-like carbon material for high capacity lithium-oxygen batteries.

    PubMed

    Li, Jing; Zhang, Huamin; Zhang, Yining; Wang, Meiri; Zhang, Fengxiang; Nie, Hongjiao

    2013-06-01

    A micron-sized honeycomb-like carbon material (MHC) is prepared in a facile way using nano-CaCO3 as a hard template. A novel electrode for lithium-oxygen batteries is fabricated and displays a superior discharge capacity as high as 5862 mA h g(-1). The higher electrode space utilization is attributed to its hierarchical pore structure, with intrinsic mesopores in the MHC particles for Li2O2 depositions and macropores among them for oxygen transport.

  16. Amine-Oxide Hybrid Materials for CO2 Capture from Ambient Air.

    PubMed

    Didas, Stephanie A; Choi, Sunho; Chaikittisilp, Watcharop; Jones, Christopher W

    2015-10-20

    Oxide supports functionalized with amine moieties have been used for decades as catalysts and chromatographic media. Owing to the recognized impact of atmospheric CO2 on global climate change, the study of the use of amine-oxide hybrid materials as CO2 sorbents has exploded in the past decade. While the majority of the work has concerned separation of CO2 from dilute mixtures such as flue gas from coal-fired power plants, it has been recognized by us and others that such supported amine materials are also perhaps uniquely suited to extract CO2 from ultradilute gas mixtures, such as ambient air. As unique, low temperature chemisorbents, they can operate under ambient conditions, spontaneously extracting CO2 from ambient air, while being regenerated under mild conditions using heat or the combination of heat and vacuum. This Account describes the evolution of our activities on the design of amine-functionalized silica materials for catalysis to the design, characterization, and utilization of these materials in CO2 separations. New materials developed in our laboratory, such as hyperbranched aminosilica materials, and previously known amine-oxide hybrid compositions, have been extensively studied for CO2 extraction from simulated ambient air (400 ppm of CO2). The role of amine type and structure (molecular, polymeric), support type and structure, the stability of the various compositions under simulated operating conditions, and the nature of the adsorbed CO2 have been investigated in detail. The requirements for an effective, practical air capture process have been outlined and the ability of amine-oxide hybrid materials to meet these needs has been discussed. Ultimately, the practicality of such a "direct air capture" process is predicated not only on the physicochemical properties of the sorbent, but also how the sorbent operates in a practical process that offers a scalable gas-solid contacting strategy. In this regard, the utility of low pressure drop monolith

  17. Amine-Oxide Hybrid Materials for CO2 Capture from Ambient Air.

    PubMed

    Didas, Stephanie A; Choi, Sunho; Chaikittisilp, Watcharop; Jones, Christopher W

    2015-10-20

    Oxide supports functionalized with amine moieties have been used for decades as catalysts and chromatographic media. Owing to the recognized impact of atmospheric CO2 on global climate change, the study of the use of amine-oxide hybrid materials as CO2 sorbents has exploded in the past decade. While the majority of the work has concerned separation of CO2 from dilute mixtures such as flue gas from coal-fired power plants, it has been recognized by us and others that such supported amine materials are also perhaps uniquely suited to extract CO2 from ultradilute gas mixtures, such as ambient air. As unique, low temperature chemisorbents, they can operate under ambient conditions, spontaneously extracting CO2 from ambient air, while being regenerated under mild conditions using heat or the combination of heat and vacuum. This Account describes the evolution of our activities on the design of amine-functionalized silica materials for catalysis to the design, characterization, and utilization of these materials in CO2 separations. New materials developed in our laboratory, such as hyperbranched aminosilica materials, and previously known amine-oxide hybrid compositions, have been extensively studied for CO2 extraction from simulated ambient air (400 ppm of CO2). The role of amine type and structure (molecular, polymeric), support type and structure, the stability of the various compositions under simulated operating conditions, and the nature of the adsorbed CO2 have been investigated in detail. The requirements for an effective, practical air capture process have been outlined and the ability of amine-oxide hybrid materials to meet these needs has been discussed. Ultimately, the practicality of such a "direct air capture" process is predicated not only on the physicochemical properties of the sorbent, but also how the sorbent operates in a practical process that offers a scalable gas-solid contacting strategy. In this regard, the utility of low pressure drop monolith

  18. Coupled modeling of water transport and air-droplet interaction in the electrode of a proton exchange membrane fuel cell

    NASA Astrophysics Data System (ADS)

    Esposito, Angelo; Pianese, Cesare; Guezennec, Yann G.

    In this work, an accurate and computationally fast model for liquid water transport within a proton exchange membrane fuel cell (PEMFC) electrode is developed by lumping the space-dependence of the relevant variables. Capillarity is considered as the main transport mechanism within the gas diffusion layer (GDL). The novelty of the model lies in the coupled simulation of the water transport at the interface between gas diffusion layer and gas flow channel (GFC). This is achieved with a phenomenological description of the process that allows its simulation with relative simplicity. Moreover, a detailed two-dimensional visualization of such interface is achieved via geometric simulation of water droplets formation, growth, coalescence and detachment on the surface of the GDL. The model is useful for optimization analysis oriented to both PEMFC design and balance of plant. Furthermore, the accomplishment of reduced computational time and good accuracy makes the model suitable for control strategy implementation to ensure PEM fuel cells operation within optimal electrode water content.

  19. A solvent-free microbial-activated air cathode battery paper platform made with pencil-traced graphite electrodes

    NASA Astrophysics Data System (ADS)

    Lee, Seung Ho; Ban, Ju Yeon; Oh, Chung-Hun; Park, Hun-Kuk; Choi, Samjin

    2016-06-01

    We present the fabrication of an ultra-low cost, disposable, solvent-free air cathode all-paper microbial fuel cell (MFC) that does not utilize any chemical treatments. The anode and cathode were fabricated by depositing graphite particles by drawing them on paper with a pencil (four strokes). Hydrophobic parchment paper was used as a proton exchange membrane (PEM) to allow only H+ to pass. Air cathode MFC technology, where O2 was used as an electron acceptor, was implemented on the paper platform. The bioelectric current was generated by an electrochemical process involving the redox couple of microbial-activated extracellular electron transferred electrons, PEM-passed H+, and O2 in the cathode. A fully micro-integrated pencil-traced MFC showed a fast start-time, producing current within 10 s after injection of bacterial cells. A single miniaturized all-paper air cathode MFC generated a maximum potential of 300 mV and a maximum current of 11 μA during 100 min after a single injection of Shewanella oneidensis. The micro-fabricated solvent-free air cathode all-paper MFC generated a power of 2,270 nW (5.68 mW/m2). The proposed solvent-free air cathode paper-based MFC device could be used for environmentally-friendly energy storage as well as in single-use medical power supplies that use organic matter.

  20. A solvent-free microbial-activated air cathode battery paper platform made with pencil-traced graphite electrodes

    PubMed Central

    Lee, Seung Ho; Ban, Ju Yeon; Oh, Chung-Hun; Park, Hun-Kuk; Choi, Samjin

    2016-01-01

    We present the fabrication of an ultra-low cost, disposable, solvent-free air cathode all-paper microbial fuel cell (MFC) that does not utilize any chemical treatments. The anode and cathode were fabricated by depositing graphite particles by drawing them on paper with a pencil (four strokes). Hydrophobic parchment paper was used as a proton exchange membrane (PEM) to allow only H+ to pass. Air cathode MFC technology, where O2 was used as an electron acceptor, was implemented on the paper platform. The bioelectric current was generated by an electrochemical process involving the redox couple of microbial-activated extracellular electron transferred electrons, PEM-passed H+, and O2 in the cathode. A fully micro-integrated pencil-traced MFC showed a fast start-time, producing current within 10 s after injection of bacterial cells. A single miniaturized all-paper air cathode MFC generated a maximum potential of 300 mV and a maximum current of 11 μA during 100 min after a single injection of Shewanella oneidensis. The micro-fabricated solvent-free air cathode all-paper MFC generated a power of 2,270 nW (5.68 mW/m2). The proposed solvent-free air cathode paper-based MFC device could be used for environmentally-friendly energy storage as well as in single-use medical power supplies that use organic matter. PMID:27333815

  1. A solvent-free microbial-activated air cathode battery paper platform made with pencil-traced graphite electrodes.

    PubMed

    Lee, Seung Ho; Ban, Ju Yeon; Oh, Chung-Hun; Park, Hun-Kuk; Choi, Samjin

    2016-06-23

    We present the fabrication of an ultra-low cost, disposable, solvent-free air cathode all-paper microbial fuel cell (MFC) that does not utilize any chemical treatments. The anode and cathode were fabricated by depositing graphite particles by drawing them on paper with a pencil (four strokes). Hydrophobic parchment paper was used as a proton exchange membrane (PEM) to allow only H(+) to pass. Air cathode MFC technology, where O2 was used as an electron acceptor, was implemented on the paper platform. The bioelectric current was generated by an electrochemical process involving the redox couple of microbial-activated extracellular electron transferred electrons, PEM-passed H(+), and O2 in the cathode. A fully micro-integrated pencil-traced MFC showed a fast start-time, producing current within 10 s after injection of bacterial cells. A single miniaturized all-paper air cathode MFC generated a maximum potential of 300 mV and a maximum current of 11 μA during 100 min after a single injection of Shewanella oneidensis. The micro-fabricated solvent-free air cathode all-paper MFC generated a power of 2,270 nW (5.68 mW/m(2)). The proposed solvent-free air cathode paper-based MFC device could be used for environmentally-friendly energy storage as well as in single-use medical power supplies that use organic matter.

  2. A solvent-free microbial-activated air cathode battery paper platform made with pencil-traced graphite electrodes.

    PubMed

    Lee, Seung Ho; Ban, Ju Yeon; Oh, Chung-Hun; Park, Hun-Kuk; Choi, Samjin

    2016-01-01

    We present the fabrication of an ultra-low cost, disposable, solvent-free air cathode all-paper microbial fuel cell (MFC) that does not utilize any chemical treatments. The anode and cathode were fabricated by depositing graphite particles by drawing them on paper with a pencil (four strokes). Hydrophobic parchment paper was used as a proton exchange membrane (PEM) to allow only H(+) to pass. Air cathode MFC technology, where O2 was used as an electron acceptor, was implemented on the paper platform. The bioelectric current was generated by an electrochemical process involving the redox couple of microbial-activated extracellular electron transferred electrons, PEM-passed H(+), and O2 in the cathode. A fully micro-integrated pencil-traced MFC showed a fast start-time, producing current within 10 s after injection of bacterial cells. A single miniaturized all-paper air cathode MFC generated a maximum potential of 300 mV and a maximum current of 11 μA during 100 min after a single injection of Shewanella oneidensis. The micro-fabricated solvent-free air cathode all-paper MFC generated a power of 2,270 nW (5.68 mW/m(2)). The proposed solvent-free air cathode paper-based MFC device could be used for environmentally-friendly energy storage as well as in single-use medical power supplies that use organic matter. PMID:27333815

  3. Effect of pH in a Pd-based ethanol membraneless air breathing nanofluidic fuel cell with flow-through electrodes

    NASA Astrophysics Data System (ADS)

    López-Rico, C. A.; Galindo-de-la-Rosa, J.; Ledesma-García, J.; Arriaga, L. G.; Guerra-Balcázar, M.; Arjona, N.

    2015-12-01

    In this work, a nanofluidic fuel cell (NFC) in which streams flow through electrodes was used to investigate the role of pH in the cell performance using ethanol as fuel and two Pd nanoparticles as electrocatalysts: one commercially available (Pd/C from ETEK) and other synthesized using ionic liquids (Pd/C IL). The cell performances for both electrocatalysts in acid/acid (anodic/cathodic) streams were of 18.05 and 9.55 mW cm-2 for Pd/C ETEK and Pd/C IL. In alkaline/alkaline streams, decrease to 15.94 mW cm-2 for Pd/C ETEK and increase to 15.37 mW cm-2 for Pd/C IL. In alkaline/acidic streams both electrocatalysts showed similar cell voltages (up to 1 V); meanwhile power densities were of 87.6 and 99.4 mW cm-2 for Pd/C ETEK and Pd/C IL. The raise in cell performance can be related to a decrease in activation losses, the combined used of alkaline and acidic streams and these high values compared with flow-over fuel cells can be related to the enhancement of the cathodic mass transport by using three dimensional porous electrodes and two sources of oxygen: from air and from a saturated solution.

  4. Effect of mesocelluar carbon foam electrode material on performance of vanadium redox flow battery

    NASA Astrophysics Data System (ADS)

    Jeong, Sanghyun; An, Sunhyung; Jeong, Jooyoung; Lee, Jinwoo; Kwon, Yongchai

    2015-03-01

    Languid reaction rate of VO2+/VO2+ redox couple is a problem to solve for improving performance of vanadium redox flow battery (VRFB). To facilitate the slow reaction materials including large pore sized mesocellular carbon foam (MSU-F-C and Pt/MSU-F-C) are used as new catalyst. Their catalytic activity and reaction reversibility are estimated and compared with other catalysts, while cycle tests of charge-discharge and polarization curve tests are implemented to evaluate energy efficiency (EE) and maximum power density (MPD). Their crystal structure, specific surface area and catalyst morphology are measured by XRD, BET and TEM. The new catalysts indicate high peak current ratio, small peak potential difference and high electron transfer rate constant, proving that their catalytic activity and reaction reversibility are superior. Regarding the charge-discharge and polarization curve tests, the VRFB single cells including new catalysts show high EE as well as low overpotential and internal resistance and high MPD. Such excellent results are due to mostly unique characteristics of MSU-F-C having large interconnected mesopores, high surface area and large contents of hydroxyl groups that serve as active sites for VO2+/VO2+ redox reaction and platinums (Pts) supporting the MSU-F-C. Indeed, employment of the catalysts including MSU-F-C leads to enhancement in performance of VRFB by facilitating the slow VO2+/VO2+ redox reaction.

  5. Porous silicon as a potential electrode material in a nerve repair setting: Tissue reactions.

    PubMed

    Johansson, Fredrik; Wallman, Lars; Danielsen, Nils; Schouenborg, Jens; Kanje, Martin

    2009-07-01

    We compared porous silicon (pSi) with smooth Si as chip-implant surfaces in a nerve regeneration setting. Silicon chips can be used for recording neural activity and are potential nerve interface devices. A silicon chip with one smooth and one porous side inserted into a tube was used to bridge a 5 mm defect in rat sciatic nerve. Six or 12 weeks later, new nerve structures surrounded by a perineurium-like capsule had formed on each side of the chip. The number of regenerated nerve fibers did not differ on either side of the chip as shown by immunostaining for neurofilaments. However, the capsule that had formed in contact with the chip was significantly thinner on the porous side than on the smooth side. Cellular protrusions had formed on the pSi side and the regenerated nerve tissue was found to attach firmly to this surface, while the tissue was hardly attached to the smooth silicon surface. We conclude that a pSi surface, due to its large surface area, diminished inflammatory response and firm adhesion to the tissue, should be a good material for the development of new implantable electronic nerve devices.

  6. Capacitive de-ionization electrode

    SciTech Connect

    Daily, III, William D.

    2013-03-19

    An electrode "cell" for use in a capacitive deionization (CDI) reactor consists of the electrode support structure, a non-reactive conductive material, the electrode accompaniment or substrate and a flow through screen/separator. These "layers" are repeated and the electrodes are sealed together with gaskets between two end plates to create stacked sets of alternating anode and cathode electrodes in the CDI reactor.

  7. Negative electrode composition

    DOEpatents

    Kaun, Thomas D.; Chilenskas, Albert A.

    1982-01-01

    A secondary electrochemical cell and a negative electrode composition for use therewith comprising a positive electrode containing an active material of a chalcogen or a transiton metal chalcogenide, a negative electrode containing a lithium-aluminum alloy and an amount of a ternary alloy sufficient to provide at least about 5 percent overcharge capacity relative to a negative electrode solely of the lithium-aluminum alloy, the ternary alloy comprising lithium, aluminum, and iron or cobalt, and an electrolyte containing lithium ions in contact with both of the positive and the negative electrodes. The ternary alloy is present in the electrode in the range of from about 5 percent to about 50 percent by weight of the electrode composition and may include lithium-aluminum-nickel alloy in combination with either the ternary iron or cobalt alloys. A plurality of series connected cells having overcharge capacity can be equalized on the discharge side without expensive electrical equipment.

  8. Hybrids of NiCo2O4 nanorods and nanobundles with graphene as promising electrode materials for supercapacitors.

    PubMed

    Wang, Zhuo; Zhang, Xin; Zhang, Zhongshen; Qiao, Nanli; Li, Yang; Hao, Zhengping

    2015-12-15

    High dispersion of NiCo2O4 nanorods and porous NiCo2O4 nanobundles decorated on RGO have been synthesized by a facile hydrothermal method, followed by calcination in one step. By adjusting the starting metal sources to realize the synthesis of different morphologies of NiCo2O4. The morphology and the microstructure of the as-prepared composites were characterized by X-ray diffraction (XRD), Brunauer-Emmett-Teller (BET) and transmission electron microscope (TEM) techniques. Among them, the porous RGO/NiCo2O4 nanobundles gives a higher specific capacitance of 1278F/g at 1A/g and 719F/g at 20A/g, showing a remarkable rate capability. The excellent electrochemical performances could ascribed to the unique structural feature with higher surface area. It could be anticipated that the synthesized electrode material will gain promising applications in supercapacitors and other devices because of their outstanding characteristics of controllable capacitance and facilely synthesized.

  9. New tris- and pentakis-fused donors containing extended tetrathiafulvalenes: New positive electrode materials for rechargeable batteries

    PubMed Central

    Iwamoto, Shintaro; Inatomi, Yuu; Ogi, Daisuke; Shibayama, Satoshi; Murakami, Yukiko; Kato, Minami; Takahashi, Kazuyuki; Tanaka, Kazuyoshi; Hojo, Nobuhiko

    2015-01-01

    Summary Derivatives of tris-fused TTF extended with two ethanediylidenes (5), tris- and pentakis-fused TTFs extended with two thiophene-2,5-diylidenes (6–9) were successfully synthesized. Cyclic voltammograms of the tetrakis(n-hexylthio) derivative of 5 and 7 (5d, 7d) consisted of two pairs of two-electron redox waves and two pairs of one-electron redox waves. On the other hand, four pairs of two-electron redox waves and two pairs of one-electron redox waves were observed for the tetrakis(n-hexylthio) derivative of 9 (9d). Coin-type cells using the bis(ethylenedithio) derivatives of 5 (5b), 6 (6b) and the tetrakis(methylthio) derivatives of 5 (5c) and 8 (8c) as positive electrode materials showed initial discharge capacities of 157–190 mAh g−1 and initial energy densities of 535–680 mAh g−1. The discharge capacities after 40 cycles were 64–86% of the initial discharge capacities. PMID:26199670

  10. Effect of the top electrode materials on the resistive switching characteristics of TiO{sub 2} thin film

    SciTech Connect

    Oh, Sang Chul; Jung, Ho Yong; Lee, Heon

    2011-06-15

    Various metals, such as Pt, stainless steel (SUS), Al, Ni, and Ti, were used as a top electrode (TE) to evaluate the dependency of the resistive switching characteristics on the TE of the metal/TiO{sub 2}/Pt structure. The variation of the chemical composition of TiO{sub 2} in the metal/TiO{sub 2}/Pt structure before and after switching was examined to identify the factors affecting the resistive switching characteristics of the samples with various TE materials. In the case of TE/TiO{sub 2}/Pt structures showing unstable resistive switching behavior, e.g., those with the Al, Ni, and Ti TEs, secondary ion mass spectrometry revealed an increase in the oxygen concentration at the interface area between the TE metal and TiO{sub 2}. This suggests that the oxidation reaction at the interface between the TE metal and TiO{sub 2} might cause the TE/TiO{sub 2}/Pt structure to exhibit unstable resistive switching characteristics. According to these results, the oxidation reaction at the interface between the metal TE and TiO{sub 2} thin film is a primary factor affecting the resistive switching characteristics of TiO{sub 2}-based Resistive Random Access Memory devices.

  11. Charge Carrier Transport Through the Interface Between Hybrid Electrodes and Organic Materials in Flexible Organic Light Emitting Diodes.

    PubMed

    Zhou, Huanyu; Cheong, Hahn-Gil; Park, Jin-Woo

    2016-05-01

    We investigated the electronic properties of composite-type hybrid transparent conductive electrodes (h-TCEs) based on Ag nanowire networks (AgNWs) and indium tin oxide (ITO). These h-TCEs were developed to replace ITO, and their mechanical flexibility is superior to that of ITO. However, the characteristics of charge carriers and the mechanism of charge-carrier transport through the interface between the h-TCE and an organic material are not well understood when the h-TCE is used as the anode in a flexible organic light-emitting diode (f-OLED). AgNWs were spin coated onto polymer substrates, and ITO was sputtered atop the AgNWs. The electronic energy structures of h-TCEs were investigated by ultraviolet photoelectron spectroscopy. f-OLEDs were fabricated on both h-TCEs and ITO for comparison. The chemical bond formation at the interface between the h-TCE and the organic layer in f-OLEDs was investigated by X-ray photoelectron spectroscopy. The performances of f-OLEDs were compared based on the analysis results. PMID:27483896

  12. Magnesium substitution to improve the electrochemical performance of layered Li2MnO3 positive-electrode material

    NASA Astrophysics Data System (ADS)

    Zhao, Wei; Xiong, Lilong; Xu, Youlong; Xiao, Xiang; Wang, Jisheng; Ren, Zaihuang

    2016-10-01

    Li2MnO3 has received lots of attention due to its large theoretical capacity. However, its application is obstructed by low practical capacity and poor cycling stability. Here, a new tactic of magnesium substitution for partial lithium to improve the electrochemical performance of Li2MnO3 by a traditional solid state reaction is presented. Sample with only 1% magnesium content delivers a large initial discharge capacity of 307.5 mAh g-1 which is much superior than the 241.9 mAh g-1 of pristine Li2MnO3. The cycling performance also get improved that the capacity retention is 84.5% for Li1.98Mg0.01MnO3 but only 77.7% for pristine counterpart after 30 cycles at 0.1 C. Moreover, the effective suppression of voltage decay has been achieved because of improved kinetic properties and leads to a tremendous progress in the energy density which is as much as 944 Wh kg-1 for Li1.98Mg0.01MnO3 compared with 747.1 Wh kg-1 of Li2MnO3. These achievements attained by Mg-doping make Li2MnO3 a promising positive-electrode material for the next generation of lithium ion batteries.

  13. Mesoporous activated carbon fiber as electrode material for high-performance electrochemical double layer capacitors with ionic liquid electrolyte

    NASA Astrophysics Data System (ADS)

    Xu, Bin; Wu, Feng; Chen, Renjie; Cao, Gaoping; Chen, Shi; Yang, Yusheng

    Activated carbon fibers (ACFs) with super high surface area and well-developed small mesopores have been prepared by pyrolyzing polyacrylonitrile fibers and NaOH activation. Their capacitive performances at room and elevated temperatures are evaluated in electrochemical double layer capacitors (EDLCs) using ionic liquid (IL) electrolyte composed of lithium bis(trifluoromethane sulfone)imide (LiN(SO 2CF 3) 2) and 2-oxazolidinone (C 3H 5NO 2). The surface area of the ACF is as high as 3291 m 2 g -1. The pore volume of the carbon reaches 2.162 cm 3 g -1, of which 66.7% is the contribution of the small mesopores of 2-5 nm. The unique microstructures enable the ACFs to have good compatibility with the IL electrolyte. The specific capacitance reaches 187 F g -1 at room temperature with good cycling and self-discharge performances. As the temperature increases to 60 °C, the capacitance increases to 196 F g -1, and the rate capability is dramatically improved. Therefore, the ACF can be a promising electrode material for high-performance EDLCs.

  14. New tris- and pentakis-fused donors containing extended tetrathiafulvalenes: New positive electrode materials for rechargeable batteries.

    PubMed

    Iwamoto, Shintaro; Inatomi, Yuu; Ogi, Daisuke; Shibayama, Satoshi; Murakami, Yukiko; Kato, Minami; Takahashi, Kazuyuki; Tanaka, Kazuyoshi; Hojo, Nobuhiko; Misaki, Yohji

    2015-01-01

    Derivatives of tris-fused TTF extended with two ethanediylidenes (5), tris- and pentakis-fused TTFs extended with two thiophene-2,5-diylidenes (6-9) were successfully synthesized. Cyclic voltammograms of the tetrakis(n-hexylthio) derivative of 5 and 7 (5d, 7d) consisted of two pairs of two-electron redox waves and two pairs of one-electron redox waves. On the other hand, four pairs of two-electron redox waves and two pairs of one-electron redox waves were observed for the tetrakis(n-hexylthio) derivative of 9 (9d). Coin-type cells using the bis(ethylenedithio) derivatives of 5 (5b), 6 (6b) and the tetrakis(methylthio) derivatives of 5 (5c) and 8 (8c) as positive electrode materials showed initial discharge capacities of 157-190 mAh g(-1) and initial energy densities of 535-680 mAh g(-1). The discharge capacities after 40 cycles were 64-86% of the initial discharge capacities. PMID:26199670

  15. NOVEL ELECTRODE MATERIALS FOR LOW-TEMPERATURE SOLID-OXIDE FUEL CELLS

    SciTech Connect

    Shaowu Zha; Luis Aguilar; Meilin Liu

    2003-12-01

    Fuel cell performance depends strongly on the anode microstructure, which is determined by the anode compositions and fabrication conditions. Four types of anodes with two kinds of NiO and GDC powders were investigated. By carefully adjusting the anode microstructure, the GDC electrolyte/anode interfacial polarization resistances reduced dramatically. The interfacial resistance at 600 C decreased from 1.61 {Omega} cm{sup 2} for the anodes prepared using commercially available powders to 0.06 {Omega} cm{sup 2} for those prepared using powders derived from a glycine-nitrate process. The critical issues facing the development of economically competitive SOFC systems include lowering the operation temperature and creating novel anode materials and microstructures capable of efficiently utilizing hydrocarbon fuels. Anode-supported SOFCs with an electrolyte of 20 {micro}m- thick Gd-doped ceria (GDC) were fabricated by co-pressing, and both Ni- and Cu-based anodes were prepared by a solution impregnation process. At 600 C, SOFCs fueled with humidified H{sub 2}, methane, and propane, reached peak power densities of 602, 519, and 433 mW/cm{sup 2}, respectively. Both microstructure and composition of the anodes, as fabricated using a solution impregnation technique, greatly influence fuel cell performance. Although steam reforming or partial oxidation is effective in avoiding carbon deposition of hydrocarbon fuels, it increases the operating cost and reduces the energy efficiency. A catalyst (1 %wt Pt dispersed on porous Gd-doped ceria) for pre-reforming of propane was developed with relatively low steam to carbon (S/C) ratio ({approx}0.5), coupled with direct utilization of the reformate in low-temperature SOFCs. Propane was converted to smaller molecules during pre-reforming, including H{sub 2}, CH{sub 4}, CO, and CO{sub 2}. A peak power density of 247 mW/cm{sup 2} was observed when pre-reformed propane was directly fed to an SOFC operated at 600 C. No carbon deposition

  16. Electrodes for microfluidic applications

    DOEpatents

    Crocker, Robert W.; Harnett, Cindy K.; Rognlien, Judith L.

    2006-08-22

    An electrode device for high pressure applications. These electrodes, designed to withstand pressure of greater than 10,000 psi, are adapted for use in microfluidic devices that employ electrokinetic or electrophoretic flow. The electrode is composed, generally, of an outer electrically insulating tubular body having a porous ceramic frit material disposed in one end of the outer body. The pores of the porous ceramic material are filled with an ion conductive polymer resin. A conductive material situated on the upper surface of the porous ceramic frit material and, thus isolated from direct contact with the electrolyte, forms a gas diffusion electrode. A metal current collector, in contact with the gas diffusion electrode, provides connection to a voltage source.

  17. Scalable Fabrication of Nanoporous Carbon Fiber Films as Bifunctional Catalytic Electrodes for Flexible Zn-Air Batteries.

    PubMed

    Liu, Qin; Wang, Yaobing; Dai, Liming; Yao, Jiannian

    2016-04-20

    A flexible nanoporous carbon-fiber film for wearable electronics is prepared by a facile and scalable method through pyrolysis of electrospun polyimide. It exhibits excellent bifunctional electrocatalytic activities for oxygen reduction and oxygen evolution. Flexible rechargeable zinc-air batteries based on the carbon-fiber film show high round-trip efficiency and mechanical stability.

  18. Determination of partition behavior of organic surrogates between paperboard packaging materials and air.

    PubMed

    Triantafyllou, V I; Akrida-Demertzi, K; Demertzis, P G

    2005-06-01

    The suitability of recycled paperboard packaging materials for direct food contact applications is a major area of investigation. Chemical contaminants (surrogates) partitioning between recycled paper packaging and foods may affect the safety and health of the consumer. The partition behavior of all possible organic compounds between cardboards and individual foodstuffs is difficult and too time consuming for being fully investigated. Therefore it may be more efficient to determine these partition coefficients indirectly through experimental determination of the partitioning behavior between cardboard samples and air. In this work, the behavior of organic pollutants present in a set of two paper and board samples intended to be in contact with foods was studied. Adsorption isotherms have been plotted and partition coefficients between paper and air have been calculated as a basis for the estimation of their migration potential into food. Values of partition coefficients (Kpaper/air) from 47 to 1207 were obtained at different temperatures. For the less volatile surrogates such as dibutyl phthalate and methyl stearate higher Kpaper/air values were obtained. The adsorption curves showed that the more volatile substances are partitioning mainly in air phase and increasing the temperature from 70 to 100 degrees C their concentrations in air (Cair) have almost doubled. The analysis of surrogates was performed with a method based on solvent extraction and gas chromatographic-flame ionization detection (GC-FID) quantification. PMID:15988989

  19. Paradoxical air embolism following contrast material injection through power injectors in patients with a patent foramen ovale.

    PubMed

    Yeddula, Kalpana; Ahmad, Iftikhar; Mohammed, Shafaath Husain Syed; Hedgire, Sandeep; Venkatesh, Vikram; Abbara, Suhny; Kalva, Sanjeeva P

    2012-12-01

    In patients with a patent foramen ovale, use of air filters during intravenous infusions is common, but they are not compatible with power injection. Therefore we aimed to assess the incidence of paradoxical air embolism on CT of the chest and brain following contrast material injection through a power injector in patients with a patent foramen ovale, without the use of a filter. In this IRB approved, HIPAA compliant retrospective study, two independent radiologists reviewed 289 CT scans of the chest (n = 233) and brain (n = 56) for vascular air embolism following contrast material injection through a power injector in 93 subjects (43 men, mean age 66 y) with a known patent foramen ovale. The location and amount of the air were assessed. The medical records were reviewed for embolic symptoms. The prevalence and location of right sided and systemic luminal air were determined and inter-observer agreement for detection of intraluminal vascular air was calculated. Vascular air embolism was observed in 19.3% (56/289) of the studies; small in 52 and moderate in 4. In 42 studies, intravascular air was seen in a single territory and 14 studies had intravascular air in multiple territories. None had air in the left side of the heart or brain to suggest paradoxical air embolism. The inter-observer agreement for detection of vascular air was moderate (k = 0.6). Paradoxical air embolism in patients with a patent foramen ovale following contrast material injection with a power injector is rare.

  20. A hierarchical three-dimensional NiCo2O4 nanowire array/carbon cloth as an air electrode for nonaqueous Li-air batteries.

    PubMed

    Liu, Wei-Ming; Gao, Ting-Ting; Yang, Yin; Sun, Qian; Fu, Zheng-Wen

    2013-10-14

    A 3D NiCo2O4 nanowire array/carbon cloth (NCONW/CC) was employed as the cathode for Li-air batteries with a non-aqueous electrolyte. After its discharge, novel porous ball-like Li2O2 was found to be deposited on the tip of NiCo2O4 nanowires. The special structure of Li2O2 and active sites of catalysts are also discussed.