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Sample records for nickel oxide electrode

  1. Factors Affecting Nickel-oxide Electrode Capacity in Nickel-hydrogen Cells

    NASA Technical Reports Server (NTRS)

    Ritterman, P. F.

    1984-01-01

    The nickel-oxide electrode common to the nickel hydrogen and nickel cadmium cell is by design the limiting or capacity determining electrode on both charge and discharge. The useable discharge capacity from this electrode, and since it is the limiting electrode, the useable discharge capacity of the cell as well, can and is optimized by rate of charge, charge temperature and additives to electrode and electrolyte. Recent tests with nickel hydrogen cells and tests performed almost 25 years ago with nickel cadmium cells indicate an improvement of capacity as a result of using increased electrolyte concentration.

  2. Nickel anode electrode

    DOEpatents

    Singh, Prabhakar; Benedict, Mark

    1987-01-01

    A nickel anode electrode fabricated by oxidizing a nickel alloying material to produce a material whose exterior contains nickel oxide and whose interior contains nickel metal throughout which is dispersed the oxide of the alloying material and by reducing and sintering the oxidized material to form a product having a nickel metal exterior and an interior containing nickel metal throughout which is dispersed the oxide of the alloying material.

  3. Ruthenium oxide modified nickel electrode for ascorbic acid detection.

    PubMed

    Lee, Yuan-Gee; Liao, Bo-Xuan; Weng, Yu-Ching

    2017-04-01

    Electrodes of ruthenium oxide modified nickel were prepared by a thermal decomposition method. The stoichiometry of the modifier, RuOx, was quantitatively determined to be a meta-stable phase, RuO5. The electrodes were employed to sense ascorbic acid in alkaline solution with a high sensitivity, 296 μAcm(-2) mM(-1), and good selectivity for eight kinds of disturbing reagents. We found that the ascorbic acid was oxidized irreversibly in solution. To match with the variation of the morphology, the sensitivity reached a maximum when the RuOx segregated with a nano-crystalline feature. We find that the substrate oxidized as the deposited RuOx grew thicker. The feature of the deposited RuOx changed from nano-particles to small islands resulting from the wetting effect of the substrate oxide, NiO; meanwhile the sensitivity decreased dramatically. The endurance of the RuOx/Ni electrode also showed a good performance after 38 days of successive test.

  4. Electrocatalytic oxidation of formaldehyde on nickel ion implanted-modified indium tin oxide electrode

    NASA Astrophysics Data System (ADS)

    Yu, Yanan; Su, Wen; Yuan, Mengwei; Fu, Yingyi; Hu, Jingbo

    2015-07-01

    This work investigates formaldehyde (HCHO) oxidation on a novel nickel ion implanted-modified indium tin oxide electrode (NiNPs/ITO). The modified electrode exhibits high electrochemical activity with Ni ions at the fluences of 10 × 1016 ions cm-2. The size of nickel nanoparticles (NiNPs) is in the range of 15-40 nm determined by scanning electron microscope (SEM). The electrochemical behaviors of the modified electrode are characterized by cyclic voltammetry (CV). In alkaline medium (i.e. NaOH 0.1 M), a good redox behavior of Ni(III)/Ni(II) couple at the surface of modified electrodes can be observed. Electrochemical performances are measured by electrochemical impedance spectroscopy (EIS) and chronoamperometric. The NiNPs/ITO electrode shows prominent electrocatalytic activity towards the oxidation of formaldehyde with long-term stability, which can be a suitable electrode material in formaldehyde fuel cells.

  5. Fuel electrode containing pre-sintered nickel/zirconia for a solid oxide fuel cell

    DOEpatents

    Ruka, Roswell J.; Vora, Shailesh D.

    2001-01-01

    A fuel cell structure (2) is provided, having a pre-sintered nickel-zirconia fuel electrode (6) and an air electrode (4), with a ceramic electrolyte (5) disposed between the electrodes, where the pre-sintered fuel electrode (6) contains particles selected from the group consisting of nickel oxide, cobalt and cerium dioxide particles and mixtures thereof, and titanium dioxide particles, within a matrix of yttria-stabilized zirconia and spaced-apart filamentary nickel strings having a chain structure, and where the fuel electrode can be sintered to provide an active solid oxide fuel cell.

  6. Study of nickel electrode oxidation as a function of 80% depth of discharge cycling

    SciTech Connect

    Pickett, D.F. Jr.; Scoles, D.L.; Johnson, Z.W.; Hayden, J.W.; Pennington, R.D.

    1997-12-31

    Oxidation of nickel sinter used in nickel oxide electrodes in aerospace nickel cadmium cells leads to hydrogen gassing and the potential for cell rupture. The oxidation is directly related to loss of overcharge protection built into the cell during manufacturing. In nickel hydrogen cells, excessive oxidation of the nickel sinter can eventually lead to a burst before leak situation and is a potential source of failure. It is well known that nickel cadmium cells having nylon separators contribute to loss of overcharge via a hydrolysis reaction of the nylon in the potassium hydroxide electrolyte environment in the cell. The hydrolysis reaction produces lower chain organics which are oxidized by the positive electrode and oxygen. Oxidation of the organics diminishes the overcharge protection. With introduction of the Super NiCd{trademark} and the Magnum{trademark} nickel cadmium cells the nylon hydrolysis reaction is eliminated, but any reducing agent in the cell such as nickel or an organic additive can contribute to loss of overcharge protection. The present effort describes chemical analyses made to evaluate the extent of overcharge protection loss in nickel cadmium cells which do not have nylon hydrolysis, and quantifies the amount of hydrogen buildup in nickel hydrogen cells which are subjected to 80% depth of discharge cycling with and without the presence of cadmium in the positive electrode.

  7. Preparation of nickel nanowire arrays electrode for urea electro-oxidation in alkaline medium

    NASA Astrophysics Data System (ADS)

    Guo, Fen; Ye, Ke; Cheng, Kui; Wang, Guiling; Cao, Dianxue

    2015-03-01

    Fully metallic nickel nanowire arrays (NWAs) electrode is prepared by electrodepositing nickel within the pores and over-plating on the surface of polycarbonate template (PCT) with subsequent dissolution of the template in dichloromethane. The as-prepared electrode is characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM) and transmission electron microscopy (TEM). Urea electro-oxidation reaction in KOH solution on the nickel NWAs electrode is investigated by cyclic voltammetry (CV), chronoamperometry (CA) and electrochemical impedance spectroscopy (EIS) tests. The results show that the nickel NWAs electrode achieves an onset oxidation potential of 0.25 V (vs. Ag/AgCl) and a peak current density of 160 mA cm-2 in 5 mol L-1 KOH and 0.33 mol L-1 urea accompanied with considerable stability.

  8. Production method of nickel electrode

    NASA Technical Reports Server (NTRS)

    Ikeda, H.; Ohira, T.

    1982-01-01

    A nickel electrode having improved charging efficiency, an increased coefficient of discharging utilization, and large capacity is disclosed. Nickel hydroxide or nickel oxide is retained in a porous nickel substrate which is immersed in an aqueous solution of cobalt acetate with a pH 4.0 to 6.8. The electrode thus obtained is then immersed in an alkaline solution or heated to change cobalt acetate into cobalt hydroxide or cobalt oxide whereby the surface of nickel active material is covered with cobalt crystals and alloying of cobalt and nickel is promoted at the same time.

  9. Electrooxidation of aliphatic alcohols on electrodes consisting of hydrophobicized supports coated with nickel oxides

    SciTech Connect

    Chaenko, N.V.; Kornienko, V.L.; Avrutskaya, I.A.; Fioshin, M.Ya.

    1987-12-01

    Two methods are presented to intensify the electrooxidation of aliphatic alcohols with low water solubility and to simplify end-product separation. One method comprised direct addition of higher nickel oxides to the active material of the electrode to be fabricated; the other involved depositing a layer of higher nickel oxides on a hydrophobicized support consisting of a mixture of a conducting material and the FP-4D hydrophobicizer. Electrolysis was carried out in a diaphragm-free two-compartment cell, one reagent and the other the electrolyte. Results are shown of hexyl alcohol oxidation on various composition supports coated with higher nickel oxides.

  10. Effect of sinter fracture and ohmic resistance on capacity retention in the nickel oxide electrode

    NASA Technical Reports Server (NTRS)

    Lanzi, Oscar; Landau, Uziel

    1991-01-01

    The lifetime of batteries which utilize the nickel oxide electrode is often limited because this electrode loses a significant portion of its capacity as it is cycled. It is asserted that this capacity loss may often be attributed to cracking or separation of the conductive nickel sinter in the electrode, which forces electronic current to pass through the poorly conducting hydrated oxide and thus imposes a significant ohmic resistance. The model indicates that the oxide develops a nearly insulating layer which prevents complete discharge in the cycled electrode at usable rates. The capacity retention can be improved by reducing the cyclic stresses or strengthening the current collecting structure, redistributing it to provide a shorter current path through the solid phase, or by increasing the conductivity of the oxide to delay the formation of an insulating layer.

  11. Effect of sinter fracture and ohmic resistance on capacity retention in the nickel oxide electrode

    NASA Technical Reports Server (NTRS)

    Lanzi, Oscar; Landau, Uziel

    1991-01-01

    The lifetime of batteries which utilize the nickel oxide electrode is often limited because this electrode loses a significant portion of its capacity as it is cycled. It is asserted that this capacity loss may often be attributed to cracking or separation of the conductive nickel sinter in the electrode, which forces electronic current to pass through the poorly conducting hydrated oxide and thus imposes a significant ohmic resistance. The model indicates that the oxide develops a nearly insulating layer which prevents complete discharge in the cycled electrode at usable rates. The capacity retention can be improved by reducing the cyclic stresses or strengthening the current collecting structure, redistributing it to provide a shorter current path through the solid phase, or by increasing the conductivity of the oxide to delay the formation of an insulating layer.

  12. ESCA investigations on plastic-bonded nickel oxide electrodes

    NASA Astrophysics Data System (ADS)

    Jindra, J.; Krejčí, I.; Mrha, J.; Folkesson, B.; Johansson, L. Y.; Larsson, R.

    Electrode samples, prepared by a rolling technique from an active mass, graphite and Teflon mixture, were characterized by ESCA (X-ray photoelectron spectroscopy) before operation, after a short electrochemical formation, and after a certain number of charge—discharge cycles. The spectra of F 1s, C 1s, O 1s and Ni 2p 3/2 were measured in detail. A splitting of the F and C signals (from Teflon) in the Teflon—graphite mixture was interpreted as indicating different qualities of contacts between the Teflon and graphite particles. The change in character of this contact resulting from cycling of the electrode was followed and was considered to be the cause of the change of the electric resistance in the electrode. From the decrease of the intensity of the Ni signal one can conclude that part of the Ni(OH) 2/NiO(OH) system withdraws from the surface of the graphite particle structure during prolonged operation of the electrode. This effect is caused by a partial crystallization of the hydrated Ni(II)Ni(III) oxide system which, in its turn, causes discontinuities in the hydrogel to appear, reflected by an increase in the F 1s signal intensity.

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

    NASA Technical Reports Server (NTRS)

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

    1986-01-01

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

  14. Electrochemical degradation of 4-chlorophenol at nickel-antimony doped tin oxide electrode.

    PubMed

    Wang, Y H; Chan, K Y; Li, X Y; So, S K

    2006-11-01

    The effectiveness of a novel nickel-antimony doped tin oxide electrode for electrochemical degradation of organic pollutants was investigated using 4-chlorophenol (4-CP) as a model toxic organic. The experimental results demonstrate that the optimal Ni content was at Ni:Sn=1:500 in atomic ratio in the precursor coating solution, whereas the Sb:Sn ratio was set at 8:500. Using the electrode prepared with the optimal Ni doping ratio for 4-CP degradation, the charge-based efficiencies were up to 89 microg C(-1) for 4-CP destruction and 15 microg C(-1) for TOC removal, which were considerably higher than the efficiencies observed for other electrodes. It is suggested that the enhancement of the electrode for electrochemical oxidation of organics could be attributed to the production of hydroxyl radicals in anodic water electrolysis.

  15. Graphene-passivated nickel as an oxidation-resistant electrode for spintronics.

    PubMed

    Dlubak, Bruno; Martin, Marie-Blandine; Weatherup, Robert S; Yang, Heejun; Deranlot, Cyrile; Blume, Raoul; Schloegl, Robert; Fert, Albert; Anane, Abdelmadjid; Hofmann, Stephan; Seneor, Pierre; Robertson, John

    2012-12-21

    We report on graphene-passivated ferromagnetic electrodes (GPFE) for spin devices. GPFE are shown to act as spin-polarized oxidation-resistant electrodes. The direct coating of nickel with few layer graphene through a readily scalable chemical vapor deposition (CVD) process allows the preservation of an unoxidized nickel surface upon air exposure. Fabrication and measurement of complete reference tunneling spin valve structures demonstrate that the GPFE is maintained as a spin polarizer and also that the presence of the graphene coating leads to a specific sign reversal of the magneto-resistance. Hence, this work highlights a novel oxidation-resistant spin source which further unlocks low cost wet chemistry processes for spintronics devices.

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

    NASA Astrophysics Data System (ADS)

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

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

  17. Nickel gradient electrode

    SciTech Connect

    Zimmerman, A.H.

    1988-03-31

    This invention relates generally to rechargeable batteries, and, in particular, relates to batteries that use nickel electrodes. It provides an improved nickel electrode with a selected gradient of additive materials. The concentration of additives in the impregnating solution are controlled during impregnation such that an additive gradient is generated. In the situation where the highest ionic conductivity is needed at the current collector boundary with the active material, the electrochemical impregnating solution is initially high in additive, and at the end of impregnation has been adjusted to significantly lower additive concentration. For chemical impregnation, the electrodes are similarly dipped in solutions that are initially high in additive. This invention is suitable for conventional additives such as cobalt, cadmium, barium, manganese, and zinc. It is therefore one objective of the invention to provide an improved nickel electrode of a battery cell with an additive in the active material to increase the life of the battery cell. Another objective is to provide for an improved nickel electrode having a greater concentration of additive near the current collector of nickel.

  18. Study on the influences of reduction temperature on nickel-yttria-stabilized zirconia solid oxide fuel cell anode using nickel oxide-film electrode

    NASA Astrophysics Data System (ADS)

    Jiao, Zhenjun; Ueno, Ai; Suzuki, Yuji; Shikazono, Naoki

    2016-10-01

    In this study, the reduction processes of nickel oxide at different temperatures were investigated using nickel-film anode to study the influences of reduction temperature on the initial performances and stability of nickel-yttria-stabilized zirconia anode. Compared to conventional nickel-yttria-stabilized zirconia composite cermet anode, nickel-film anode has the advantage of direct observation at nickel-yttria-stabilized zirconia interface. The microstructural changes were characterized by scanning electron microscopy. The reduction process of nickel oxide is considered to be determined by the competition between the mechanisms of volume reduction in nickel oxide-nickel reaction and nickel sintering. Electrochemical impedance spectroscopy was applied to analyze the time variation of the nickel-film anode electrochemical characteristics. The anode performances and microstructural changes before and after 100 hours discharging and open circuit operations were analyzed. The degradation of nickel-film anode is considered to be determined by the co-effect between the nickel sintering and the change of nickel-yttria-stabilized zirconia interface bonding condition.

  19. 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.

  20. Performance of lightweight nickel electrodes

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1988-01-01

    The NASA Lewis Research Center is currently developing nickel electrodes for nickel-hydrogen (Ni-H2) batteries. These electrodes are lighter in weight and have higher energy densities than the heavier state-of-the-art (SOA) sintered nickel electrodes. In the present approach, lightweight materials or plaques are used as conductive supports for the nickel hydroxide active material. These plaques (fiber and felt, nickel plated plastic and graphite) are commercial products that are fabricated into nickel electrodes by electrochemically impregnating them with active material. Evaluation is performed in half cells structured in the bipolar configuration. Initial performance tests include capacity measurements at five discharge levels, C/2, 1.0C 1.37C, 2.0C and 2.74C. The electrodes that pass the initial tests are life cycle tested in a low Earth orbit regime at 80 percent depth of discharge. Different formulations of nickel fiber materials obtained from several manufacturers are currently being tested as possible candidates for nickel electrodes. One particular lightweight fiber mat electrode has accumulated over 3000 cycles to date, with stable capacity and voltage. Life and performance data of this electrode were investigated and presented. Good dimensional stability and active material adherence have been demonstrated in electrodes made from this lightweight plaque.

  1. Electro-oxidation and characterization of nickel foam electrode for removing boron.

    PubMed

    Kartikaningsih, Danis; Huang, Yao-Hui; Shih, Yu-Jen

    2017-01-01

    The electrocoagulation (EC) using metallic Ni foam as electrodes was studied for the removal of boron from solution. The electrolytic parameters were pH (4-12), current density (0.6-2.5 mA cm(-2)), and initial concentration of boron (10-100 mg L(-1)). Experimental results revealed that removal efficiency was maximized at pH 8-9, and decreased as the pH increased beyond that range. At particular onset potentials (0.5-0.8 V vs. Hg/HgO), the micro-granular nickel oxide that was created on the surface of the nickel metal substrate depended on pH, as determined by cyclic voltammetry. Most of the crystallites of the precipitates comprised a mixed phase of β-Ni(OH)2, a theophrastite phase, and NiOOH, as revealed by XRD and SEM analyses. A current density of 1.25 mA cm(-2) was effective in the EC of boron, and increasing the concentration of boric acid from 10 to 100 mg L(-1) did not greatly impair removal efficiency. A kinetic investigation revealed that the reaction followed a pseudo-second order rate model. The optimal conditions under which 99.2% of boron was removed from treated wastewater with 10 mg L(-1)-B, leaving less than 0.1 mg L(-1)-B in the electrolyte, were pH 8 and 1.25 mA cm(-2) for 120 min. Copyright © 2016 Elsevier Ltd. All rights reserved.

  2. Hybrid nickel manganese oxide nanosheet-3D metallic dendrite percolation network electrodes for high-rate electrochemical energy storage.

    PubMed

    Nguyen, Tuyen; Eugénio, Sónia; Boudard, Michel; Rapenne, Laetitia; Carmezim, M João; Silva, Teresa M; Montemor, M Fátima

    2015-08-07

    This work reports the fabrication, by electrodeposition and post-thermal annealing, of hybrid electrodes for high rate electrochemical energy storage composed of nickel manganese oxide (Ni0.86Mn0.14O) nanosheets over 3D open porous dendritic NiCu foams. The hybrid electrodes are made of two different percolation networks of nanosheets and dendrites, and exhibit a specific capacitance value of 848 F g(-1) at 1 A g(-1). The electrochemical tests revealed that the electrodes display an excellent rate capability, characterized by capacitance retention of approximately 83% when the applied current density increases from 1 A g(-1) to 20 A g(-1). The electrodes also evidenced high charge-discharge cycling stability, which attained 103% after 1000 cycles.

  3. Electrodeposition of palladium and reduced graphene oxide nanocomposites on foam-nickel electrode for electrocatalytic hydrodechlorination of 4-chlorophenol.

    PubMed

    Liu, Yong; Liu, Lan; Shan, Jun; Zhang, Jingdong

    2015-06-15

    A high-performance palladium (Pd) and reduced graphene oxide (RGO) composite electrode was prepared on foam-nickel (foam-Ni) via two-step electrodeposition processes. The scanning electron microscopic (SEM) observation showed that the obtained Pd/RGO/foam-Ni composite electrode displayed a uniform and compact morphology. The X-ray diffraction (XRD) and X-ray photoelectron spectroscopic (XPS) analysis confirmed the successful deposition of Pd and RGO on nickel substrate. The cyclic voltammetric (CV) measurements indicated that the presence of RGO greatly enhanced the active surface area of Pd particles deposited on foam-Ni. The as-deposited Pd/RGO/foam-Ni electrode was applied to electrocatalytic hydrodechlorination (ECH) of 4-chlorophenol (4-CP). Various factors influencing the dechlorination of 4-CP such as dechlorination current, initial concentration of 4-CP, Na2SO4 concentration and initial pH were systematically investigated. The thermodynamic analysis showed that the dechlorination reaction of 4-CP at different temperatures followed the first-order kinetics and the activation energy for 4-CP dechlorination on Pd/RGO/foam-Ni electrode was calculated to be 51.96 kJ mol(-1). Under the optimum conditions, the dechlorination efficiency of 4-CP could reach 100% after 60-min ECH treatment. Moreover, the prepared Pd/RGO/foam-Ni composite electrode showed good stability for recycling utilization in ECH of 4-CP. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. Application of Gold Electrodes for the Study of Nickel Based Homogeneous Catalysts for Hydrogen Oxidation

    SciTech Connect

    Nepomnyashchii, Alexander B.; Liu, Fei; Roberts, John A.; Parkinson, Bruce A.

    2013-08-12

    Gold and glassy carbon working electrode materials are compared as suitable substrates for the hydrogen oxidation reaction with Ni(PCy2Nt-Bu2)2(BF4)2 used as a catalyst. Voltammetric responses showing electrocatalytic hydrogen oxidation mediated by the homogeneous electrocatalyst Ni(PCy2Nt-Bu2)2(BF4)2 are identical at glassy carbon and gold electrodes, which shows that gold electrode can be used for hydrogen oxidation reaction. This work is supported as part of the Center for Molecular Electrocatalysis, an Energy Frontier Research Center funded by the US Department of Energy, Office of Science, Office of Basic Energy Sciences under FWP 56073.

  5. Disposable Non-Enzymatic Glucose Sensors Using Screen-Printed Nickel/Carbon Composites on Indium Tin Oxide Electrodes.

    PubMed

    Jeon, Won-Yong; Choi, Young-Bong; Kim, Hyug-Han

    2015-12-10

    Disposable screen-printed nickel/carbon composites on indium tin oxide (ITO) electrodes (DSPNCE) were developed for the detection of glucose without enzymes. The DSPNCE were prepared by screen-printing the ITO substrate with a 50 wt% nickel/carbon composite, followed by curing at 400 °C for 30 min. The redox couple of Ni(OH)₂/NiOOH was deposited on the surface of the electrodes via cyclic voltammetry (CV), scanning from 0-1.5 V for 30 cycles in 0.1 M NaOH solution. The DSPNCE were characterized by field-emission scanning electron microscopy (FE-SEM), X-ray photoelectron spectroscopy (XPS), and electrochemical methods. The resulting electrical currents, measured by CV and chronoamperometry at 0.65 V vs. Ag/AgCl, showed a good linear response with glucose concentrations from 1.0-10 mM. Also, the prepared electrodes showed no interference from common physiologic interferents such as uric acid (UA) or ascorbic acid (AA). Therefore, this approach allowed the development of a simple, disposable glucose biosensor.

  6. Non-Sintered Nickel Electrode

    DOEpatents

    Bernard, Patrick; Dennig, Corinne; Cocciantelli, Jean-Michel; Alcorta, Jose; Coco, Isabelle

    2002-01-01

    A non-sintered nickel electrode contains a conductive support and a paste comprising an electrochemically active material containing nickel hydroxide and a binder which is a mixture of an elastomer and a crystalline polymer. The proportion of the elastomer is in the range 25% to 60% by weight of the binder and the proportion of the crystalline polymer is in the range 40% to 75% by weight of the binder.

  7. Visibility and oxidation stability of hybrid-type copper mesh electrodes with combined nickel-carbon nanotube coating.

    PubMed

    Kim, Bu-Jong; Hwang, Young-Jin; Park, Jin-Seok

    2017-04-21

    Hybrid-type transparent conductive electrodes (TCEs) were fabricated by coating copper (Cu) meshes with carbon nanotube (CNT) via electrophoretic deposition, and with nickel (Ni) via electroplating. For the fabricated electrodes, the effects of the coating with CNT and Ni on their transmittance and reflectance in the visible-light range, electrical sheet resistance, and chromatic parameters (e.g., redness and yellowness) were characterized. Also, an oxidation stability test was performed by exposing the electrodes to air for 20 d at 85 °C and 85% temperature and humidity conditions, respectively. It was discovered that the CNT coating considerably reduced the reflectance of the Cu meshes, and that the Ni coating effectively protected the Cu meshes against oxidation. Furthermore, after the coating with CNT, both the redness and yellowness of the Cu mesh regardless of the Ni coating approached almost zero, indicating a natural color. The experiment results confirmed that the hybrid-type Cu meshes with combined Ni-CNT coating improved characteristics in terms of reflectance, sheet resistance, oxidation stability, and color, superior to those of the primitive Cu mesh, and also simultaneously satisfied most of the requirements for TCEs.

  8. The CMG Nickel Electrode

    NASA Technical Reports Server (NTRS)

    Depaul, R. A.; Gutridge, I.

    1981-01-01

    The development and design of the Controlled Microgeometry electrode are described. Advantages of the electrode over others in existance include a higher number of ampere hours per kilogram and the ability to make them over a wide range of thicknesses. The parameters that control the performance of the electrode can be individually controlled over a wide range. Therefore, the electrode may be designed to give the optimum performance for a given duty cycle.

  9. Development of a lightweight nickel electrode

    NASA Technical Reports Server (NTRS)

    Britton, D. L.; Reid, M. A.

    1984-01-01

    Nickel electrodes made using lightweight plastic plaque are about half the weight of electrodes made from state of the art sintered nickel plaque. This weight reduction would result in a significant improvement in the energy density of batteries using nickel electrodes (nickel hydrogen, nickel cadmium and nickel zinc). These lightweight electrodes are suitably conductive and yield comparable capacities (as high as 0.25 AH/gm (0.048 AH/sq cm)) after formation. These lightweight electrodes also show excellent discharge performance at high rates.

  10. Lightweight Electrode For Nickel/Hydrogen Cell

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1994-01-01

    Improved substrate for nickel electrode increases specific energy of nickel/hydrogen cell. Consists of 50 percent by weight nickel fiber, 35 percent nickel powder, and 15 percent cobalt powder. Porosity and thickness of nickel electrodes affect specific energy, initial performance, and cycle life of cell. Substrate easily manufactured with much larger porosities than those of heavy-sintered state-of-art nickel substrate.

  11. Cobalt improves nickel hydroxide electrodes for batteries

    NASA Technical Reports Server (NTRS)

    Lerner, S. R.; Seiger, H. N.

    1969-01-01

    Positive nickel hydroxide electrodes containing 20 mole percent of cobalt hydroxide are more efficient than when impregnated to the same degree by weight with nickel hydroxide alone. Charge-acceptance and oxygen-evolution tests indicate cobalt electrodes are more efficient than plain positive nickel hydroxide electrodes at all rates of charge.

  12. Migration of Co in nickel oxide/hydroxide of a nickel electrode in a Ni/H2 cell

    NASA Technical Reports Server (NTRS)

    Lim, Hong S.; Doty, Robert E.

    1993-01-01

    Cobalt redistribution in nickel active material has been reported. This redistribution was suspected to be related to capacity fading. The objective of this work is to establish a relationship between cobalt redistribution and capacity fading. Microscopic cobalt distribution in nickel active material was studied using three EDX techniques: line scan, point-by-point analysis, and dot maps. Results from this study are presented.

  13. Organic devices based on nickel nanowires transparent electrode

    PubMed Central

    Kim, Jeongmo; da Silva, Wilson Jose; bin Mohd Yusoff, Abd. Rashid; Jang, Jin

    2016-01-01

    Herein, we demonstrate a facile approach to synthesize long nickel nanowires and discuss its suitability to replace our commonly used transparent electrode, indium-tin-oxide (ITO), by a hydrazine hydrate reduction method where nickel ions are reduced to nickel atoms in an alkaline solution. The highly purified nickel nanowires show high transparency within the visible region, although the sheet resistance is slightly larger compared to that of our frequently used transparent electrode, ITO. A comparison study on organic light emitting diodes and organic solar cells, using commercially available ITO, silver nanowires, and nickel nanowires, are also discussed. PMID:26804335

  14. Organic devices based on nickel nanowires transparent electrode

    NASA Astrophysics Data System (ADS)

    Kim, Jeongmo; da Silva, Wilson Jose; Bin Mohd Yusoff, Abd. Rashid; Jang, Jin

    2016-01-01

    Herein, we demonstrate a facile approach to synthesize long nickel nanowires and discuss its suitability to replace our commonly used transparent electrode, indium-tin-oxide (ITO), by a hydrazine hydrate reduction method where nickel ions are reduced to nickel atoms in an alkaline solution. The highly purified nickel nanowires show high transparency within the visible region, although the sheet resistance is slightly larger compared to that of our frequently used transparent electrode, ITO. A comparison study on organic light emitting diodes and organic solar cells, using commercially available ITO, silver nanowires, and nickel nanowires, are also discussed.

  15. Advances in lightweight nickel electrode technology

    NASA Technical Reports Server (NTRS)

    Coates, Dwaine; Paul, Gary; Wheeler, James R.; Daugherty, Paul

    1989-01-01

    Studies are currently underway to further the development of lightweight nickel electrode technology. Work is focused primarily on the space nickel-hydrogen system and nickel-iron system but is also applicable to the nickel-cadmium and nickel-zinc systems. The goal is to reduce electrode weight while maintaining or improving performance thereby increasing electrode energy density. Two basic electrode structures are being investigated. The first is the traditional nickel sponge produced from sintered nickel-carbonyl powder and the second is a new material for this application which consists of a non-woven mat of nickel fiber. Electrodes are being manufactured, tested and evaluated at the electrode and cell level.

  16. Advances in lightweight nickel electrode technology

    NASA Technical Reports Server (NTRS)

    Coates, Dwaine; Paul, Gary; Daugherty, Paul

    1989-01-01

    Studies are currently underway to further the development of lightweight nickel electrode technology. Work is focused primarily on the space nickel-hydrogen system and nickel-iron system but is also applicable to the nickel-cadmium and nickel-zinc systems. The goal is to reduce electrode weight while maintaining or improving performance, thereby increasing electrode energy density. Two basic electrode structures are being investigated. The first is the traditional nickel sponge produced from sintered nickel-carbonyl powder. The second is a new material for this application which consists of a non-woven mat of nickel fiber. Electrodes are being manufactured, tested, and evaluated at the electrode and cell level.

  17. Degradation Mechanisms in Solid-Oxide Fuel and Electrolyzer Cells: Analytical Description of Nickel Agglomeration in a Ni /Y S Z Electrode

    NASA Astrophysics Data System (ADS)

    Kröll, L.; de Haart, L. G. J.; Vinke, I.; Eichel, R.-A.

    2017-04-01

    The microstructural evolution of a porous electrode consisting of a metal-ceramic matrix, consisting of nickel and yttria-stabilized zirconia (Y S Z ), is one of the main degradation mechanisms in a solid-oxide cell (SOC), in either fuel cell or electrolyzer mode. In that respect, the agglomeration of nickel particles in a SOC electrode leads to a decrease in the electronic conductivity as well as in the active catalytic area for the oxidation-reduction reaction of the fuel-water steam. An analytical model of the agglomeration behavior of a Ni /Y S Z electrode is proposed that allows for a quantitative description of the nickel agglomeration. The accuracy of the model is validated in terms of a comparison with experimental degradation measurements. The model is based on contact probabilities of nickel clusters in a porous network of nickel and Y S Z , derived from an algorithm of the agglomeration process. The iterative algorithm is converted into an analytical function, which involves structural parameters of the electrode, such as the porosity and the nickel content. Furthermore, to describe the agglomeration mechanism, the influence of the steam content and the flux rate are taken into account via reactions on the nickel surface. In the next step, the developed agglomeration model is combined with the mechanism of the Ostwald ripening. The calculated grain-size growth is compared to measurements at different temperatures and under low flux rates and low steam content, as well as under high flux rates and high steam content. The results confirm the necessity of connecting the two mechanisms and clarify the circumstances in which the single processes occur and how they contribute to the total agglomeration of the particles in the electrode.

  18. Electrochemical Imprinted Polycrystalline Nickel-Nickel Oxide Half-Nanotube-Modified Boron-Doped Diamond Electrode for the Detection of L-Serine.

    PubMed

    Dai, Wei; Li, Hongji; Li, Mingji; Li, Cuiping; Wu, Xiaoguo; Yang, Baohe

    2015-10-21

    This paper presents a novel and versatile method for the fabrication of half nanotubes (HNTs) using a flexible template-based nanofabrication method denoted as electrochemical imprinting. With use of this method, polycrystalline nickel and nickel(II) oxide (Ni-NiO) HNTs were synthesized using pulsed electrodeposition to transfer Ni, deposited by radio frequency magnetron sputtering on a porous polytetrafluoroethylene template, onto a boron-doped diamond (BDD) film. The Ni-NiO HNTs exhibited semicircular profiles along their entire lengths, with outer diameters of 50-120 nm and inner diameters of 20-50 nm. The HNT walls were formed of Ni and NiO nanoparticles. A biosensor for the detection of L-serine was fabricated using a BDD electrode modified with Ni-NiO HNTs, and the device demonstrated satisfactory analytical performance with high sensitivity (0.33 μA μM(-1)) and a low limit of detection (0.1 μM). The biosensor also exhibited very good reproducibility and stability, as well as a high anti-interference ability against amino acids such as L-leucine, L-tryptophan, L-cysteine, L-phenylalanine, L-arginine, and L-lysine.

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

    NASA Technical Reports Server (NTRS)

    Lerch, Bradley

    1995-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Lerch, Bradley

    1995-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1995-01-01

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

  2. Lightweight Nickel Electrode Development Program

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1998-01-01

    Because of its relatively high specific energy and excellent cycling capability, the nickel-hydrogen (Ni-H2) cell is used extensively to store energy in aerospace systems. For the past several years, the NASA Lewis Research Center has been developing the Ni-H2 cell to improve its components, design, and operating characteristics. The battery size and weight are crucial parameters in aerospace and spacecraft power systems for applications such as the International Space Station, space satellites, and space telescopes. The nickel electrode has been identified as the heaviest and most critical component of the Ni-H2 cell. Consequently, Lewis began and is leading a program to reduce the electrode's weight by using lightweight plaques.

  3. Aluminum-doped lithium nickel cobalt oxide electrodes for high-power lithium-ion batteries

    NASA Astrophysics Data System (ADS)

    Chen, C. H.; Liu, J.; Stoll, M. E.; Henriksen, G.; Vissers, D. R.; Amine, K.

    Non-doped and aluminum-doped LiNi 0.8Co 0.2O 2 cathodes from three industrial developers coupled with graphite anodes were made into lithium-ion cells for high-power applications. The powder morphology of the active cathode materials was examined by a scanning electron microscope. The electrochemical performance of these cells was investigated by hybrid pulse power characterization (HPPC) testing, accelerated aging, and AC impedance measurement of symmetric cells. Although all of the fresh cells are found to meet and exceed the power requirements set by PNGV, the power capability of those cells with non-doped LiNi 0.8Co 0.2O 2 cathodes fades rapidly due to the rise of the cell impedance. Al-doping is found very effective to suppress the cell impedance rise by stabilizing the charge-transfer impedance on the cathode side. The stabilization mechanism may be related to the low average oxidation state of nickel ions in the cathode. The powder morphology also plays a secondary role in determining the impedance stabilization.

  4. New Method for the Deposition of Nickel Oxide in Porous Scaffolds for Electrodes in Solid Oxide Fuel Cells and Electrolyzers.

    PubMed

    Ruiz-Trejo, Enrique; Puolamaa, Milla; Sum, Brian; Tariq, Farid; Yufit, Vladimir; Brandon, Nigel P

    2017-01-10

    A simple chemical bath deposition is used to coat a complex porous ceramic scaffold with a conformal Ni layer. The resulting composite is used as a solid oxide fuel cell electrode, and its electrochemical response is measured in humidified hydrogen. X-ray tomography is used to determine the microstructural characteristics of the uncoated and Ni-coated porous structure, which include the surface area to total volume, the radial pore size, and the size of the necks between the pores.

  5. Lightweight fibrous nickel electrodes for nickel-hydrogen batteries

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1989-01-01

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

  6. Mesoporous composite nickel cobalt oxide/graphene oxide synthesized via a template-assistant co-precipitation route as electrode material for supercapacitors

    NASA Astrophysics Data System (ADS)

    Xu, Yanjie; Wang, Lincai; Cao, Peiqi; Cai, Chuanlin; Fu, Yanbao; Ma, Xiaohua

    2016-02-01

    A simple co-precipitation method utilizing SDS (sodium dodecyl sulfate) as template and ammonia as precipitant is successfully employed to synthesize nickel cobalt oxide/graphene oxide (NiCo2O4/GO) composite. The as-prepared composite (NCG-10) exhibits a high capacitance of 1211.25 F g-1, 687 F g-1 at the current density of 1 A g-1, 10 A g-1 and good cycling ability which renders NCG-10 as promising electrode material for supercapacitors. An asymmetric supercapacitor (ASC) (full button cell) has been constructed with NCG-10 as positive electrode and lab-made reduced graphene oxide (rGO) as negative electrode. The fabricated NCG-10//rGO with an extended stable operational voltage of 1.6 V can deliver a high specific capacitance of 144.45 F g-1 at a current density of 1 A g-1. The as-prepared NCG-10//rGO demonstrates remarkable energy density (51.36 W h kg-1 at 1 A g-1), high power density (50 kW kg-1 at 20 A g-1). The retention of capacitance is 88.6% at the current density of 8 A g-1 after 2000 cycles. The enhanced capacitive performance can be attributed to the improved specific surface area and 3D open area of NCG-10 generated by the pores and channels with the substantial function of SDS.

  7. Exploring Lithium-Cobalt-Nickel-Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells

    SciTech Connect

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C.; Wu, Jinsong; Dravid, Vinayak P.; Yan, Pengfei; Wang, Chong-Min; Kim, Soo; Wolverton, Chris; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R.; Thackeray, Michael M.

    2016-10-19

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi(2)MnO(3)center dot(1-x)LiMO2 (M = Ni, Mn, or Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to that of manganese and nickel ions in close-packed oxides and (2) their higher potential (similar to 3.6 V vs Li0) relative to manganese oxide spinels (similar to 2.9 V vs Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO(2) (0 <= x <= 0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNi(x)O(2) structures when prepared in air between 400 and 800 degrees C and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentrations, offer the possibility of improving the cycling stability, energy, and power of high energy (>= 3.5 V) lithium-ion cells.

  8. Exploring Lithium-Cobalt-Nickel-Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells.

    PubMed

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C; Wu, Jinsong; Dravid, Vinayak P; Yan, Pengfei; Wang, Chongmin; Kim, Soo; Wolverton, Christopher; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R; Thackeray, Michael Makepeace

    2016-10-04

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3●(1-x)LiMO2 (M=Ni, Mn, Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to manganese and nickel ions in close-packed oxides and (2) their higher potential (~3.6 V vs. Li(0)) relative to manganese oxide spinels (~2.9 V vs. Li(0)) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we have revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0≤x≤0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures, when prepared in air between 400 and 800 °C, and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentration, offer the possibility of improving the cycling stability, energy, and power of high energy (≥3.5 V) lithium-ion cells.

  9. Exploring Lithium-Cobalt-Nickel-Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells

    DOE PAGES

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C.; ...

    2016-10-19

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi(2)MnO(3)center dot(1-x)LiMO2 (M = Ni, Mn, or Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to that of manganese and nickel ions in close-packed oxides and (2) their higher potential (similar to 3.6 V vs Li0) relative to manganese oxide spinels (similar tomore » 2.9 V vs Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO(2) (0 <= x <= 0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNi(x)O(2) structures when prepared in air between 400 and 800 degrees C and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentrations, offer the possibility of improving the cycling stability, energy, and power of high energy (>= 3.5 V) lithium-ion cells.« less

  10. Exploring Lithium-Cobalt-Nickel Oxide Spinel Electrodes for ≥3.5 V Li-Ion Cells

    SciTech Connect

    Lee, Eungje; Blauwkamp, Joel; Castro, Fernando C.; Wu, Jinsong; Dravid, Vinayak P.; Yan, Pengfei; Wang, Chongmin; Kim, Soo; Wolverton, Christopher; Benedek, Roy; Dogan, Fulya; Park, Joong Sun; Croy, Jason R.; Thackeray, Michael M.

    2016-10-19

    Recent reports have indicated that a manganese oxide spinel component, when embedded in a relatively small concentration in layered xLi2MnO3(1-x)LiMO2 (M=Ni, Mn, Co) electrode systems, can act as a stabilizer that increases their capacity, rate capability, cycle life, and first-cycle efficiency. These findings prompted us to explore the possibility of exploiting lithiated cobalt oxide spinel stabilizers by taking advantage of (1) the low mobility of cobalt ions relative to manganese and nickel ions in close-packed oxides and (2) their higher potential (~3.6 V vs. Li0) relative to manganese oxide spinels (~2.9 V vs. Li0) for the spinel-to-lithiated spinel electrochemical reaction. In particular, we have revisited the structural and electrochemical properties of lithiated spinels in the LiCo1-xNixO2 (0x0.2) system, first reported almost 25 years ago, by means of high-resolution (synchrotron) X-ray diffraction, transmission electron microscopy, nuclear magnetic resonance spectroscopy, electrochemical cell tests, and theoretical calculations. The results provide a deeper understanding of the complexity of intergrown layered/lithiated spinel LiCo1-xNixO2 structures, when prepared in air between 400 and 800 C, and the impact of structural variations on their electrochemical behavior. These structures, when used in low concentration, offer the possibility of improving the cycling stability, energy, and power of high energy (≥3.5 V) lithium-ion cells.

  11. The zinc electrode - Its behaviour in the nickel oxide-zinc accumulator

    NASA Astrophysics Data System (ADS)

    Certain aspects of zinc electrode reaction and behavior are investigated in view of their application to batteries. The properties of the zinc electrode in a battery system are discussed, emphasizing porous structure. Shape change is emphasized as the most important factor leading to limited battery cycle life. It is shown that two existing models of shape change based on electroosmosis and current distribution are unable to consistently describe observed phenomena. The first stages of electrocrystallization are studied and the surface reactions between the silver substrate and the deposited zinc layer are investigated. The reaction mechanism of zinc and amalgamated zinc in an alkaline electrolyte is addressed, and the batter system is studied to obtain information on cycling behavior and on the shape change phenomenon. The effect on cycle behavior of diferent amalgamation techniques of the zinc electrode and several additives is addressed. Impedance measurements on zinc electrodes are considered, and battery behavior is correlated with changes in the zinc electrode during cycling.

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

    NASA Technical Reports Server (NTRS)

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

    1996-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    1996-01-01

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

  14. DNA/nickel oxide nanoparticles/osmium(III)-complex modified electrode toward selective oxidation of l-cysteine and simultaneous detection of l-cysteine and homocysteine.

    PubMed

    Sharifi, Ensiyeh; Salimi, Abdollah; Shams, Esmaeil

    2012-08-01

    The modification of glassy carbon (GC) electrode with electrodeposited nickel oxide nanoparticles (NiOxNPs) and deoxyribonucleic acid (DNA) is utilized as a new efficient platform for entrapment of osmium (III) complex. Surface morphology and electrochemical properties of the prepared nanocomposite modified electrode (GC/DNA/NiOxNPs/Os(III)-complex) were investigated by FESEM, cyclic voltammetry and electrochemical impedance spectroscopy techniques. Cyclic voltammetric results indicated the excellent electrocatalytic activity of the resulting electrode toward oxidation of l-cysteine (CySH) at reduced overpotential (0.1 V vs. Ag/AgCl). Using chronoamperometry to CySH detection, the sensitivity and detection limit of the biosensor are obtained as 44 μA mM(-1) and 0.07 μM with a concentration range up to 1000 μM. The electrocatalytic activity of the modified electrode not only for oxidation of low molecular-mass biothiols derivatives such as, glutathione, l-cystine, l-methionine and electroactive biological species ( dopamine, uric acid, glucose) is negligible but also for very similar biothiol compound (homocysteine) no recognizable response is observed at the applied potential window. Furthermore, the simultaneous voltammetric determination of l-cysteine and homocysteine compounds without any separation or pretreatment process was reported for the first time in this work. Finally, the applicability of sensor for the analysis of CySH concentration in complex serum samples was successfully demonstrated. Highly selectivity, excellent electrocatalytic activity and stability, remarkable antifouling property toward thiols and their oxidation products, as well as the ability for simultaneous detection of l-cysteine and homocysteine are remarkably advantageous of the proposed DNA based biosensor.

  15. Partial conversion of current collectors into nickel copper oxide electrode materials for high-performance energy storage devices.

    PubMed

    Zhang, Liuyang; Gong, Hao

    2015-07-22

    A novel substrate sacrifice process is proposed and developed for converting part of a current collector into supercapacitor active materials, which provides a new route in achieving high energy density of supercapacitor device. Part of a copper foam current collector is successfully converted into highly porous nickel copper oxide electrode for light- and high-performance supercapacitors. Remarkably, this strategy circumvents the problem associated with poor contact interface between electrode and current collector. Meanwhile, the overall weight of the supercapacitor could be minimized. The charge transfer kinetics is improved while the advantage of the excellent mechanical properties of metal current collector is not traded off. By virtue of this unique current collector self-involved architecture, the material derived from the current collector manifests large areal capacitance of 3.13 F cm(-2) at a current density of 1 A g(-1). The capacitance can retain 2.97 F cm(-2) at a much higher density (4 A g(-1)). Only a small decay of 6.5% appears at 4 A g(-1) after 1600 cycles. The strategy reported here sheds light on new strategies in making additional use of the metal current collector. Furthermore, asymmetric supercapacitor using both solid-state gel electrolyte and liquid counterpart are obtained and analyzed. The liquid asymmetric supercapacitor can deliver a high energy density up to 0.5 mWh cm(-2) (53 Wh kg(-1)) at a power density of 13 mW cm(-2) (1.4 kW kg(-1)).

  16. Method of manufacturing positive nickel hydroxide electrodes

    DOEpatents

    Gutjahr, M.A.; Schmid, R.; Beccu, K.D.

    1975-12-16

    A method of manufacturing a positive nickel hydroxide electrode is discussed. A highly porous core structure of organic material having a fibrous or reticular texture is uniformly coated with nickel powder and then subjected to a thermal treatment which provides sintering of the powder coating and removal of the organic core material. A consolidated, porous nickel support structure is thus produced which has substantially the same texture and porosity as the initial core structure. To provide the positive electrode including the active mass, nickel hydroxide is deposited in the pores of the nickel support structure.

  17. Lightweight nickel electrode for nickel hydrogen cells and batteries

    NASA Technical Reports Server (NTRS)

    Britton, D. L.

    1986-01-01

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

  18. Lightweight nickel electrode for nickel hydrogen cells and batteries

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1986-01-01

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

  19. New Method for the Deposition of Nickel Oxide in Porous Scaffolds for Electrodes in Solid Oxide Fuel Cells and Electrolyzers

    PubMed Central

    Puolamaa, Milla; Sum, Brian; Tariq, Farid; Yufit, Vladimir; Brandon, Nigel P.

    2016-01-01

    Abstract A simple chemical bath deposition is used to coat a complex porous ceramic scaffold with a conformal Ni layer. The resulting composite is used as a solid oxide fuel cell electrode, and its electrochemical response is measured in humidified hydrogen. X‐ray tomography is used to determine the microstructural characteristics of the uncoated and Ni‐coated porous structure, which include the surface area to total volume, the radial pore size, and the size of the necks between the pores. PMID:27739632

  20. High-performance binder-free supercapacitor electrode by direct growth of cobalt-manganese composite oxide nansostructures on nickel foam

    PubMed Central

    2014-01-01

    A facile approach composed of hydrothermal process and annealing treatment is proposed to directly grow cobalt-manganese composite oxide ((Co,Mn)3O4) nanostructures on three-dimensional (3D) conductive nickel (Ni) foam for a supercapacitor electrode. The as-fabricated porous electrode exhibits excellent rate capability and high specific capacitance of 840.2 F g-1 at the current density of 10 A g-1, and the electrode also shows excellent cycling performance, which retains 102% of its initial discharge capacitance after 7,000 cycles. The fabricated binder-free hierarchical composite electrode with superior electrochemical performance is a promising candidate for high-performance supercapacitors. PMID:25258611

  1. High-performance binder-free supercapacitor electrode by direct growth of cobalt-manganese composite oxide nansostructures on nickel foam.

    PubMed

    Jiang, Shulan; Shi, Tielin; Long, Hu; Sun, Yongming; Zhou, Wei; Tang, Zirong

    2014-01-01

    A facile approach composed of hydrothermal process and annealing treatment is proposed to directly grow cobalt-manganese composite oxide ((Co,Mn)3O4) nanostructures on three-dimensional (3D) conductive nickel (Ni) foam for a supercapacitor electrode. The as-fabricated porous electrode exhibits excellent rate capability and high specific capacitance of 840.2 F g(-1) at the current density of 10 A g(-1), and the electrode also shows excellent cycling performance, which retains 102% of its initial discharge capacitance after 7,000 cycles. The fabricated binder-free hierarchical composite electrode with superior electrochemical performance is a promising candidate for high-performance supercapacitors.

  2. Long Life Nickel Electrodes for Nickel-Hydrogen Cells: Fiber Substrates Nickel Electrodes

    NASA Technical Reports Server (NTRS)

    Rogers, Howard H.

    2000-01-01

    Samples of nickel fiber mat electrodes were investigated over a wide range of fiber diameters, electrode thickness, porosity and active material loading levels. Thickness' were 0.040, 0.060 and 0.080 inches for the plaque: fiber diameters were primarily 2, 4, and 8 micron and porosity was 85, 90, and 95%. Capacities of 3.5 in. diameter electrodes were determined in the flooded condition with both 26 and 31% potassium hydroxide solution. These capacity tests indicated that the highest capacities per unit weight were obtained at the 90% porosity level with a 4 micron diameter fiber plaque. It appeared that the thinner electrodes had somewhat better performance, consistent with sintered electrode history. Limited testing with two-positive-electrode boiler plate cells was also carried out. Considerable difficulty with constructing the cells was encountered with short circuits the major problem. Nevertheless, four cells were tested. The cell with 95% porosity electrodes failed during conditioning cycling due to high voltage during charge. Discharge showed that this cell had lost nearly all of its capacity. The other three cells after 20 conditioning cycles showed capacities consistent with the flooded capacities of the electrodes. Positive electrodes made from fiber substrates may well show a weight advantage of standard sintered electrodes, but need considerably more work to prove this statement. A major problem to be investigated is the lower strength of the substrate compared to standard sintered electrodes. Problems with welding of leads were significant and implications that the electrodes would expand more than sintered electrodes need to be investigated. Loading levels were lower than had been expected based on sintered electrode experiences and the lower loading led to lower capacity values. However, lower loading causes less expansion and contraction during cycling so that stress on the substrate is reduced.

  3. Lightweight nickel electrodes for nickel/hydrogen cells

    NASA Technical Reports Server (NTRS)

    Lim, Hong S.; Zelter, Gabriela R.

    1993-01-01

    Thick nickel electrodes with lightweight substrate material have been prepared and tested in Ni/H2 boilerplate cells containing 26 percent KOH electrolyte. Lightweight substrates used were either 85 or 90 percent in porosity and either 0.8 or 2 mm in thickness, respectively, compared with 80 to 82 percent porosity and 0.75 to 0.8 mm thickness of the state-of-the-art sintered plaque substrate. All of these thick electrodes had substantially improved theoretical (or chemical) capacity over that of state-of-the-art sintered nickel plaque electrodes. However, utilization of the active material was low (65 to 80 percent) compared with that of the state-of-the-art electrodes (approximately 90 percent) in 26 percent KOH. Due to this low utilization, the electrodes using 85 percent porous substrates did not show any advantage over the state-of-the-art ones. The electrodes using a 90 percent porous substrate, however, showed 17 percent higher usable specific capacity (about 0.13 Ah/g in 26 percent KOH) than that of the state-of-the-art nickel electrodes despite the low utilization. These electrodes achieved up to 4860 cycles at 40 percent depth-of-discharge with neither capacity loss nor any significant changes of rate capability and charging efficiency with cycling.

  4. Progress in the development of lightweight nickel electrode

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1992-01-01

    The use of the lightweight nickel electrode, in place of the heavy-sintered state-of-the-art nickel electrode, will lead to improvements in specific energy and performance of the nickel-hydrogen cell. Preliminary testing indicates that a nickel fiber mat is a promising support candidate for the nickel hydroxide active material. Nickel electrodes made from fiber mats, with nickel and cobalt powder added to the fiber, were tested at LeRC. To date, over 8000 cycles have been accumulated, at 40 percent depth-of-discharge, using the lightweight fiber electrode, in a boiler plate nickel-hydrogen cell.

  5. High-Performance Supercapacitor Electrode Based on Cobalt Oxide-Manganese Dioxide-Nickel Oxide Ternary 1D Hybrid Nanotubes.

    PubMed

    Singh, Ashutosh K; Sarkar, Debasish; Karmakar, Keshab; Mandal, Kalyan; Khan, Gobinda Gopal

    2016-08-17

    We report a facile method to design Co3O4-MnO2-NiO ternary hybrid 1D nanotube arrays for their application as active material for high-performance supercapacitor electrodes. This as-prepared novel supercapacitor electrode can store charge as high as ∼2020 C/g (equivalent specific capacitance ∼2525 F/g) for a potential window of 0.8 V and has long cycle stability (nearly 80% specific capacitance retains after successive 5700 charge/discharge cycles), significantly high Coulombic efficiency, and fast response time (∼0.17s). The remarkable electrochemical performance of this unique electrode material is the outcome of its enormous reaction platform provided by its special nanostructure morphology and conglomeration of the electrochemical properties of three highly redox active materials in a single unit.

  6. Review on advances in porous nanostructured nickel oxides and their composite electrodes for high-performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Sk, Md Moniruzzaman; Yue, Chee Yoon; Ghosh, Kalyan; Jena, Rajeeb Kumar

    2016-03-01

    Recently, porous nanostructured transition metal oxides with excellent electrochemical performance have become a new class of energy storage materials for supercapacitors. The ever-growing global demand of electrically powered devices makes it imperative to develop renewable, efficient and reliable electrochemical energy storage devices. This review article focuses on the Ni based transition metal oxides and their composite electrode materials including carbons, metals and transition metal oxides for supercapacitor applications, providing an overview on the charge mechanisms, methodologies and nanostructures discovered in recent years, and latest research findings. The NiO and their composites possess higher reversible capacity, good structural stability, and have been studied for usage as novel electrode materials for supercapacitors. Their fine-tuned physical and chemical properties make them ideal candidates for supercapacitor applications as they possess higher accessible electroactive sites, which will provide both high power density and also high energy density. Moreover, synergistic effects can be derived from the constituent materials of the NiO based composite electrodes. The potential problems like device fabrication, measurement techniques, and future prospects of utilizing these materials as supercapacitor electrodes highlighting the fundamental understanding of the relationship between electrochemical and structural performances are also discussed.

  7. The effects of platinum on nickel electrodes in the nickel hydrogen cell

    NASA Technical Reports Server (NTRS)

    Zimmerman, Albert H.

    1991-01-01

    Interactions of platinum and platinum compounds with the nickel electrode that are possible in the nickel hydrogen cell, where both the nickel electrode and a platinum catalyst hydrogen electrode are in intimate contact with the alkaline electrolyte, are examined. Additionally, a mechanism of nickel cobalt oxyhydroxide formation in NiH2 cells is presented.

  8. Electrochemical investigation of the voltammetric determination of hydrochlorothiazide using a nickel hydroxide modified nickel electrode.

    PubMed

    Machini, Wesley B S; David-Parra, Diego N; Teixeira, Marcos F S

    2015-12-01

    The preparation and electrochemical characterization of a nickel hydroxide modified nickel electrode as well as its behavior as electrocatalyst toward the oxidation of hydrochlorothiazide (HCTZ) were investigated. The electrochemical behavior of the modified electrode and the electrooxidation of HCTZ were explored using cyclic voltammetry. The voltammetric response of the modified electrode in the detection of HCTZ is based on the electrochemical oxidation of the Ni(II)/Ni(III) and a chemical redox process. The analytical parameters for the electrooxidation of HCTZ by the nickel hydroxide modified nickel electrode were obtained in NaOH solution, in which the linear voltammetric response was in the concentration range from 1.39×10(-5) to 1.67×10(-4)mol L(-1) with a limit of detection of 7.92×10(-6)mol L(-1) and a sensitivity of 0.138 μA Lmmol(-1). Tafel analysis was used to elucidate the kinetics and mechanism of HCTZ oxidation by the modified electrode.

  9. Self-templated Synthesis of Nickel Silicate Hydroxide/Reduced Graphene Oxide Composite Hollow Microspheres as Highly Stable Supercapacitor Electrode Material

    NASA Astrophysics Data System (ADS)

    Zhang, Yanhua; Zhou, Wenjie; Yu, Hong; Feng, Tong; Pu, Yong; Liu, Hongdong; Xiao, Wei; Tian, Liangliang

    2017-05-01

    Nickel silicate hydroxide/reduced graphene oxide (Ni3Si2O5(OH)4/RGO) composite hollow microspheres were one-pot hydrothermally synthesized by employing graphene oxide (GO)-wrapped SiO2 microspheres as the template and silicon source, which were prepared through sonication-assisted interfacial self-assembly of tiny GO sheets on positively charged SiO2 substrate microspheres. The composition, morphology, structure, and phase of Ni3Si2O5(OH)4/RGO microspheres as well as their electrochemical properties were carefully studied. It was found that Ni3Si2O5(OH)4/RGO microspheres featured distinct hierarchical porous morphology with hollow architecture and a large specific surface area as high as 67.6 m2 g-1. When utilized as a supercapacitor electrode material, Ni3Si2O5(OH)4/RGO hollow microspheres released a maximum specific capacitance of 178.9 F g-1 at the current density of 1 A g-1, which was much higher than that of the contrastive bare Ni3Si2O5(OH)4 hollow microspheres and bare RGO material developed in this work, displaying enhanced supercapacitive behavior. Impressively, the Ni3Si2O5(OH)4/RGO microsphere electrode exhibited outstanding rate capability and long-term cycling stability and durability with 97.6% retention of the initial capacitance after continuous charging/discharging for up to 5000 cycles at the current density of 6 A g-1, which is superior or comparable to that of most of other reported nickel-based electrode materials, hence showing promising application potential in the energy storage area.

  10. Electrochemical impregnation and cycle life of lightweight nickel electrodes for nickel-hydrogen cells

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1990-01-01

    Development of a high specific energy nickel electrode is the main goal of the lightweight nickel electrode program at NASA-Lewis. The approach was to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen cell. Lightweight plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products that are fabricated into nickel electrodes by electrochemically impregnating them with active material. The electrodes are life cycle tested in a low earth orbit regime at 40 and 80 percent depths-of-discharge.

  11. Electrochemical impregnation and cycle life of lightweight nickel electrodes for nickel-hydrogen cells

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1990-01-01

    Development of a high specific energy nickel electrode is the main goal of the lightweight nickel electrode program at NASA-Lewis. The approach was to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen cell. Lightweight plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products that are fabricated into nickel electrodes by electrochemically impregnating them with active material. The electrodes are life cycle tested in a low Earth orbit regime at 40 and 80 percent depths-of-discharge.

  12. Electrochemical impregnation and cycle life of lightweight nickel electrodes for nickel-hydrogen cells

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1990-01-01

    Development of a high specific energy nickel electrode is the main goal of the lightweight nickel electrode program at NASA-Lewis. The approach was to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen cell. Lightweight plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products that are fabricated into nickel electrodes by electrochemically impregnating them with active material. The electrodes are life cycle tested in a low earth orbit regime at 40 and 80 percent depths-of-discharge.

  13. Perfluorodiethoxymethane on nickel and nickel oxide surfaces

    SciTech Connect

    Jacobson, Joyce

    1994-03-03

    The interaction of perfluorodiethoxymethane with a nickel single crystal, Ni(100); a nickel crystal with chemisorbed oxygen, Ni(100)-c(2x2)O; and a nickel crystal with nickel oxide crystallites, NiO(100) is investigated in an ultra high vacuum environment using thermal desorption spectroscopy and high resolution electron energy loss spectroscopy. Nickel, a component of hard disk drives and stainless steel, is used to represent metal surfaces in these "real" systems. Perfluorodiethoxymethane is used in this study as a model compound of industrial perfluoropolyether lubricants. These lubricants are known for their exceptional stability, except in the presence of metals. Perfluorodiethoxymethane contains the acetal group (-OCF2O-), believed to be particularly vulnerable to attack in the presence of Lewis acids. Since the surfaces studied show increasing Lewis acidity at the nickel atom sites, one might expect to see increasing decomposition of perfluorodiethoxymethane due to acidic attack of the acetal group. No decomposition of perfluorodiethoxymethane is observed on the clean Ni(100) surface, while more research is needed to determine whether a small decomposition pathway is observed on the oxygenated surfaces, or whether sample impurities are interfering with results. The strength of the bonding of perfluorodiethoxymethane to the surface is found to increase as the nickel atoms sites become more acidic in moving from Ni(100) to Ni (100)-c(2x2)O to NiO (100).

  14. Recent progress in nickel based materials for high performance pseudocapacitor electrodes

    NASA Astrophysics Data System (ADS)

    Feng, Liangdong; Zhu, Yufu; Ding, Hongyan; Ni, Chaoying

    2014-12-01

    Nickel based materials have been intensively investigated and considered as good potential electrode materials for pseudocapacitors due to their high theoretical specific capacity values, high chemical and thermal stability, ready availability, environmentally benign nature and lower cost. This review firstly examines recent progress in nickel oxides or nickel hydroxides for high performance pseudocapacitor electrodes. The advances of hybrid electrodes are then assessed to include hybrid systems of nickel based materials with compounds such as carbonaceous materials, metal and transition metal oxides or hydroxides, in which various strategies have been adopted to improve the electrical conductivity of nickel oxides or hydroxides. Furthermore, the energy density and power density of some recently reported NiO, nickel based composites and NiCo2O4 are summarized and discussed. Finally, we provide some perspectives as to the future directions of this intriguing field.

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

    NASA Technical Reports Server (NTRS)

    Britton, Doris L. (Inventor)

    2001-01-01

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

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

    NASA Technical Reports Server (NTRS)

    Britton, Doris L. (Inventor)

    2001-01-01

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

  17. High surface area, low weight composite nickel fiber electrodes

    NASA Technical Reports Server (NTRS)

    Johnson, Bradley A.; Ferro, Richard E.; Swain, Greg M.; Tatarchuk, Bruce J.

    1993-01-01

    The energy density and power density of light weight aerospace batteries utilizing the nickel oxide electrode are often limited by the microstructures of both the collector and the resulting active deposit in/on the collector. Heretofore, these two microstructures were intimately linked to one another by the materials used to prepare the collector grid as well as the methods and conditions used to deposit the active material. Significant weight and performance advantages were demonstrated by Britton and Reid at NASA-LeRC using FIBREX nickel mats of ca. 28-32 microns diameter. Work in our laboratory investigated the potential performance advantages offered by nickel fiber composite electrodes containing a mixture of fibers as small as 2 microns diameter (Available from Memtec America Corporation). These electrode collectors possess in excess of an order of magnitude more surface area per gram of collector than FIBREX nickel. The increase in surface area of the collector roughly translates into an order of magnitude thinner layer of active material. Performance data and advantages of these thin layer structures are presented. Attributes and limitations of their electrode microstructure to independently control void volume, pore structure of the Ni(OH)2 deposition, and resulting electrical properties are discussed.

  18. Structural transformation of nickel hydroxide films during anodic oxidation

    SciTech Connect

    Crocker, Robert W.; Muller, Rolf H.

    1992-05-01

    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 - 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  19. Structural transformation of nickel hydroxide films during anodic oxidation

    SciTech Connect

    Crocker, R.W.; Muller, R.H.

    1992-05-01

    The transformation of anodically formed nickel hydroxide/oxy-hydroxide electrodes has been investigated. A mechanism is proposed for the anodic oxidation reaction, in which the reaction interface between the reduced and oxidized phases of the electrode evolves in a nodular topography that leads to inefficient utilization of the active electrode material. In the proposed nodular transformation model for the anodic oxidation reaction, nickel hydroxide is oxidized to nickel oxy-hydroxide in the region near the metal substrate. Since the nickel oxy-hydroxide is considerably more conductive than the surrounding nickel hydroxide, as further oxidation occurs, nodular features grow rapidly to the film/electrolyte interface. Upon emerging at the electrolyte interface, the reaction boundary between the nickel hydroxide and oxy-hydroxide phases spreads laterally across the film/electrolyte interface, creating an overlayer of nickel oxy-hydroxide and trapping uncharged regions of nickel hydroxide within the film. The nickel oxy-hydroxide overlayer surface facilitates the oxygen evolution side reaction. Scanning tunneling microscopy of the electrode in its charged state revealed evidence of 80 {endash} 100 Angstrom nickel oxy-hydroxide nodules in the nickel hydroxide film. In situ spectroscopic ellipsometer measurements of films held at various constant potentials agree quantitatively with optical models appropriate to the nodular growth and subsequent overgrowth of the nickel oxy-hydroxide phase. A two-dimensional, numerical finite difference model was developed to simulate the current distribution along the phase boundary between the charged and uncharged material. The model was used to explore the effects of the physical parameters that govern the electrode behavior. The ratio of the conductivities of the nickel hydroxide and oxy-hydroxide phases was found to be the dominant parameter in the system.

  20. Nickel nanoparticle-chitosan-reduced graphene oxide-modified screen-printed electrodes for enzyme-free glucose sensing in portable microfluidic devices.

    PubMed

    Yang, Jiang; Yu, Ji-Hyuk; Rudi Strickler, J; Chang, Woo-Jin; Gunasekaran, Sundaram

    2013-09-15

    A facile one-step strategy is reported to synthesize nanocomposites of chitosan-reduced graphene oxide-nickel nanoparticles (CS-RGO-NiNPs) onto a screen-printed electrode (SPE). The synthesis is initiated by electrostatic and hydrophobic interactions and formation of self-assembled nanocomposite precursors of negatively charged graphene oxide (GO) and positively charged CS and nickel cations (Ni(2+)). The intrinsic mechanism of co-depositions from the nanocomposite precursor solution under cathodic potentials is based on simultaneous depositions of CS at high localized pH and in situ reduced hydrophobic RGO from GO as well as cathodically reduced metal precursors into nanoparticles. There is no need for any pre- or post-reduction of GO due to the in situ electrochemical reduction and the removal of oxygenated functionalities, which lead to an increase in hydrophobicity of RGO and successive deposition on the electrode surface. The as-prepared CS-RGO-NiNPs-modified SPE sensor exhibited outstanding performance for enzymeless glucose (Glc) sensing in alkaline media with high sensitivity (318.4µAmM(-1)cm(-2)), wide linear range (up to 9mM), low detection limit (4.1µM), acceptable selectivity against common interferents in physiological fluids, and excellent stability. A microfluidic device was fabricated incorporating the SPE sensor for real-time Glc detection in human urine samples; the results obtained were comparable to those obtained using a high-performance liquid chromatography (HPLC) coupled with an electrochemical detector. The excellent sensing performance, operational characteristics, ease of fabrication, and low cost bode well for this electrochemical microfluidic device to be developed as a point-of-care healthcare monitoring unit.

  1. Recent progress in the development of a lightweight nickel electrode

    SciTech Connect

    Britton, D.L.

    1995-12-31

    The nickel-hydrogen (Ni-H{sub 2}) cell is rapidly replacing nickel-cadmium (Ni-Cd) cell as the system of choice for aerospace applications where weight is crucial. The heavy-sintered nickel electrode used in this cell accounts for about 38% of the cell weight. The use of small diameter fiber nickel electrodes will reduce the weight and improve the specific energy of the state-of-the-art Ni-H{sub 2} cell by about 50%. One advantage of this small diameter nickel fiber material is the increase in the surface area available for the deposition of active material. Initial testing of this type of electrode is very promising. This electrode is also applicable to other nickel-based batteries, such as nickel-zinc, nickel-iron, and nickel-metal-hydride, both for space and commercial applications.

  2. Sintered electrode for solid oxide fuel cells

    DOEpatents

    Ruka, Roswell J.; Warner, Kathryn A.

    1999-01-01

    A solid oxide fuel cell fuel electrode is produced by a sintering process. An underlayer is applied to the electrolyte of a solid oxide fuel cell in the form of a slurry, which is then dried. An overlayer is applied to the underlayer and then dried. The dried underlayer and overlayer are then sintered to form a fuel electrode. Both the underlayer and the overlayer comprise a combination of electrode metal such as nickel, and stabilized zirconia such as yttria-stabilized zirconia, with the overlayer comprising a greater percentage of electrode metal. The use of more stabilized zirconia in the underlayer provides good adhesion to the electrolyte of the fuel cell, while the use of more electrode metal in the overlayer provides good electrical conductivity. The sintered fuel electrode is less expensive to produce compared with conventional electrodes made by electrochemical vapor deposition processes. The sintered electrodes exhibit favorable performance characteristics, including good porosity, adhesion, electrical conductivity and freedom from degradation.

  3. Nickel/cobalt oxide-decorated 3D graphene nanocomposite electrode for enhanced electrochemical detection of urea.

    PubMed

    Nguyen, Nhi Sa; Das, Gautam; Yoon, Hyon Hee

    2016-03-15

    A NiCo2O4 bimetallic electro-catalyst was synthesized on three-dimensional graphene (3D graphene) for the non-enzymatic detection of urea. The structural and morphological properties of the NiCo2O4/3D graphene nanocomposite were characterized by X-ray diffraction, Raman spectroscopy, and scanning electron microscopy. The NiCo2O4/3D graphene was deposited on an indium tin oxide (ITO) glass to fabricate a highly sensitive urea sensor. The electrochemical properties of the prepared electrode were studied by cyclic voltammetry. A high sensitivity of 166 μAmM(-)(1)cm(-)(2) was obtained for the NiCo2O4/3D graphene/ITO sensor. The sensor exhibited a linear range of 0.06-0.30 mM (R(2)=0.998) and a fast response time of approximately 1.0 s with a detection limit of 5.0 µM. Additionally, the sensor exhibited high stability with a sensitivity decrease of only 5.5% after four months of storage in ambient conditions. The urea sensor demonstrates feasibility for urea analysis in urine samples. Copyright © 2015 Elsevier B.V. All rights reserved.

  4. An Oxygen Electrode Based on Nickel/Cobalt Spinel,

    DTIC Science & Technology

    1981-07-01

    RESUME On a d~montr6 la formation de l oxyde mixte de cadmium et de nickel du type "spinelle" par ]a d~coposition thermique du nitrate de cadmium se...3). Metal oxide catalysts of the spinel or perovskite structure offer the possibility of high catalytic activity and extended life under a variety of...operating conditions. Tseung and co-workers (4,5) have shown that perovskite oxide electrodes prepared by doping LaCoU 3 with strontium perform

  5. Development of Sintered Fiber Nickel Electrodes for Aerospace Batteries

    NASA Technical Reports Server (NTRS)

    Francisco, Jennifer; Chiappetti, Dennis; Brill, Jack

    1997-01-01

    The nickel electrode is the specific energy limiting component in nickel battery systems. A concerted effort is currently underway to improve NiH2 performance while decreasing system cost. Increased performance with electrode specific energy (mAh/g) is the major goal of this effort. However, cost reduction is also an important part of the overall program, achieved by reducing the electrode weight. A lightweight, high energy density, nickel electrode is being, developed based on a highly porous, sintered fiber, nickel substrate. This developing technology has many applications, but is highly, applicable to the military and aerospace industries.

  6. Development of sintered fiber nickel electrodes for aerospace batteries

    SciTech Connect

    Francisco, J.; Chiappetti, D.; Brill, J.

    1997-12-01

    The nickel electrode is the specific energy limiting component in nickel battery systems. A concerted effort is currently underway to improve NiH{sub 2} performance while decreasing system cost. Increased performance with electrode specific energy (mAh/g) is the major goal of this effort. However, cost reduction is also an important part of the overall program, achieved by reducing the electrode weight. A lightweight, high energy density nickel electrode is being developed based on a highly porous, sintered fiber, nickel substrate. This developing technology has many applications, but is highly applicable to the military and aerospace industries.

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

    NASA Technical Reports Server (NTRS)

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

    2005-01-01

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

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

    NASA Technical Reports Server (NTRS)

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

    2005-01-01

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

  9. Paste Type Nickel Electrode Containing Compound And At Least One Other Element

    DOEpatents

    Bernard, Patrick; Bertrand, Fran.cedilla.oise; Simonneau, Olivier

    1999-11-30

    The present invention provides a paste type nickel electrode for a storage cell having an alkaline electrolyte, the electrode comprising a current collector and a paste containing a nickel-based hydroxide and an oxidized compound of cobalt syncrystallized with at least one other element, wherein said hydroxide forms a first powder and wherein said compound forms a second powder distinct from said first powder, said powders being mixed mechanically within said paste.

  10. Development of a micro-fiber nickel electrode for nickel-hydrogen cell

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1995-01-01

    Development of a high specific energy nickel electrode is the main goal of the lightweight nickel electrode program at the NASA Lewis Research Center. The approach has been to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen cell. Small fiber diameter nickel plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products and have an advantage of increased surface area available for the deposition of active material. Initial tests include activation and capacity measurements at different discharge levels followed by half-cell cycle testing at 80 percent depth-of-discharge in a low-Earth-orbit regime. The electrodes that pass the initial tests are life cycle-tested in a boiler plate nickel-hydrogen cell before flightweight designs are built and tested.

  11. Raman structural studies of the nickel electrode

    NASA Technical Reports Server (NTRS)

    Cornilsen, Bahne C.

    1994-01-01

    The objectives of this investigation have been to define the structures of charged active mass, discharged active mass, and related precursor materials (alpha-phases), with the purpose of better understanding the chemical and electrochemical reactions, including failure mechanisms and cobalt incorporation, so that the nickel electrode may be improved. Although our primary tool has been Raman spectroscopy, the structural conclusions drawn from the Raman data have been supported and augmented by three other analysis methods: infrared spectroscopy, powder X-ray Diffraction (XRD), and x-ray absorption spectroscopy (in particular EXAFS, Extended X-ray Absorption Fine Structure spectroscopy).

  12. Applications of x ray absorption fine structure to the in situ study of the effect of cobalt in nickel hydrous oxide electrodes for fuel cells and rechargeable batteries

    NASA Technical Reports Server (NTRS)

    Kim, Sunghyun; Tryk, Donald A.; Scherson, Daniel A.; Antonio, Mark R.

    1993-01-01

    Electronic and structural aspects of composite nickel-cobalt hydrous oxides have been examined in alkaline solutions using in situ X-ray absorption fine structure (XAFS). The results obtained have indicated that cobalt in this material is present as cobaltic ions regardless of the oxidation state of nickel in the lattice. Furthermore, careful analysis of the Co K-edge Extended X-ray absorption fine structure data reveals that the co-electrodeposition procedure generates a single phase, mixed metal hydrous oxide, in which cobaltic ions occupy nickel sites in the NiO2 sheet-like layers and not two intermixed phases each consisting of a single metal hydrous oxide.

  13. Exploring the main function of reduced graphene oxide nano-flakes in a nickel cobalt sulfide counter electrode for dye-sensitized solar cell

    NASA Astrophysics Data System (ADS)

    Lu, Man-Ning; Lin, Jeng-Yu; Wei, Tzu-Chien

    2016-11-01

    Addition of carbonaceous materials into transition metal sulfide counter electrode (CE) of a dye-sensitized solar cell (DSSC) is a common method to improve the performance of the CE and consequent photovoltaic performance. This improvement is almost without exception attributed to the improvement of overall conductivity after the carbonaceous material addition; however, the root function of these carbonaceous materials in promoting the solar cell efficiency is seldom discussed. In this study, highly crystallized nickel cobalt sulfide (NCS) micro-particles were mixed with a small portion of home-made reduced graphene oxide (rGO) nano-flakes. This NCS/rGO hybrid is subjected to extensive characterizations including X-ray diffraction, Raman spectroscopy, field emission scanning microscopy and electrochemical impedance spectroscopy. It is found that the rGO acts bi-functionally including a co-catalyst in accelerating the tri-iodide reduction for the main NCS catalysts, conductivity promotor to decrease the series resistance of the CE. Proved by electrochemical impedance spectroscopy, it is confirmed that the decrease in series resistance is less insignificant than that in charge transfer resistance, indicating rGO functions more profoundly as a co-catalyst than as a conductivity promotor. Moreover, an argument to highlight the requirement of a CE in a dim-light optimized DSSC is also proposed.

  14. Green reduction of reduced graphene oxide with nickel tetraphenyl porphyrin nanocomposite modified electrode for enhanced electrochemical determination of environmentally pollutant nitrobenzene.

    PubMed

    Kubendhiran, Subbiramaniyan; Sakthinathan, Subramanian; Chen, Shen-Ming; Tamizhdurai, P; Shanthi, K; Karuppiah, Chelladurai

    2017-07-01

    Nitrobenzene (NB) is widely used in the manufacturing of different types of products and other aromatic chemicals. Moreover, it is highly toxic and environmental pollutant compound. Therefore, the detection of nitro aromatic compounds (NACs) has gained more attention in the field of sensor. This article describes the green reduction utilized to preparation of green reduced graphene oxide/nickel tetraphenyl porphyrin (GRGO/Ni-TPP) nanocomposite modified electrode for the determination of nitrobenzene (NB). The GRGO was prepared by environmentally friendly method and using caffeic acid (CA) as a reducing agent. Moreover, the GRGO/Ni-TPP nanocomposite was prepared via the π-π stacking interaction between the RGO and Ni-TPP. In addition, the prepared material was confirmed by the UV-Visible spectroscopy (UV), nuclear magnetic resonance spectroscopy (NMR) and Fourier transform infrared spectroscopy (FTIR). The structural morphology and elemental composition of the prepared nanocomposite was confirmed by the scanning electron microscope (SEM) and energy dispersive X-ray spectroscopy (EDX). Besides, the electrochemical studies of the prepared nanocomposite was characterized by the CV and DPV technique. The DPV studies displayed the linearity response of the proposed sensor about 0.5-878µM with the sensitivity of 1.277µAµM(-1)cm(-2) and the limit of detection (LOD) is 0.14µM. Furthermore, the GRGO/Ni-TPP nanocomposite modified electrode shows good selectivity towards the detection of NB. In addition, the real sample analysis exhibited appreciable recovery towards the determination of NB using various types of water samples.

  15. Process for producing nickel electrode having lightweight substrate

    NASA Technical Reports Server (NTRS)

    Lim, Hong S. (Inventor)

    1996-01-01

    A nickel electrode having a lightweight porous nickel substrate is subjected to a formation cycle involving heavy overcharging and under-discharging in a KOH electrolyte having a concentration of 26% to 31%, resulting in electrodes displaying high active material utilization.

  16. Nongassing nickel-cadmium battery electrodes and cells

    NASA Technical Reports Server (NTRS)

    Luksha, E.; Gordy, D. J.

    1972-01-01

    The failure of nickel-cadmium storage batteries due to severe gassing during charging is discussed. In order to increase the life of such cells, nongassing positive and negative electrodes are used. The gassing characteristics of nickel electrodes were evaluated as a function of their loading, charge rate, and charge temperature.

  17. Nickel oxide nanotube synthesis using multiwalled carbon nanotubes as sacrificial templates for supercapacitor application

    NASA Astrophysics Data System (ADS)

    Abdalla, Ahmed M.; Sahu, Rakesh P.; Wallar, Cameron J.; Chen, Ri; Zhitomirsky, Igor; Puri, Ishwar K.

    2017-02-01

    A novel approach for the fabrication of nickel oxide nanotubes based on multiwalled carbon nanotubes as a sacrificial template is described. Electroless deposition is employed to deposit nickel onto carbon nanotubes. The subsequent annealing of the product in the presence of air oxidizes nickel to nickel oxide, and carbon is released as gaseous carbon dioxide, leaving behind nickel oxide nanotubes. Electron microscopy and elemental mapping confirm the formation of nickel oxide nanotubes. New chelating polyelectrolytes are used as dispersing agents to achieve high colloidal stability for both the nickel-coated carbon nanotubes and the nickel oxide nanotubes. A gravimetric specific capacitance of 245.3 F g-1 and an areal capacitance of 3.28 F cm-2 at a scan rate of 2 mV s-1 is achieved, with an electrode fabricated using nickel oxide nanotubes as the active element with a mass loading of 24.1 mg cm-2.

  18. Nickel oxide nanotube synthesis using multiwalled carbon nanotubes as sacrificial templates for supercapacitor application.

    PubMed

    Abdalla, Ahmed M; Sahu, Rakesh P; Wallar, Cameron J; Chen, Ri; Zhitomirsky, Igor; Puri, Ishwar K

    2017-02-17

    A novel approach for the fabrication of nickel oxide nanotubes based on multiwalled carbon nanotubes as a sacrificial template is described. Electroless deposition is employed to deposit nickel onto carbon nanotubes. The subsequent annealing of the product in the presence of air oxidizes nickel to nickel oxide, and carbon is released as gaseous carbon dioxide, leaving behind nickel oxide nanotubes. Electron microscopy and elemental mapping confirm the formation of nickel oxide nanotubes. New chelating polyelectrolytes are used as dispersing agents to achieve high colloidal stability for both the nickel-coated carbon nanotubes and the nickel oxide nanotubes. A gravimetric specific capacitance of 245.3 F g(-1) and  an areal capacitance of 3.28 F cm(-2) at a scan rate of 2 mV s(-1) is achieved, with an electrode fabricated using nickel oxide nanotubes as the active element with a mass loading of 24.1 mg cm(-2).

  19. Discontinuous and Continuous Processing of Low-Solvent Battery Slurries for Lithium Nickel Cobalt Manganese Oxide Electrodes

    NASA Astrophysics Data System (ADS)

    Dreger, Henning; Bockholt, Henrike; Haselrieder, Wolfgang; Kwade, Arno

    2015-11-01

    Different discontinuously and continuously working dispersing devices were investigated to determine their influence on the structural and electrochemical properties of electrodes made from commercial LiNi1/3Co1/3Mn1/3O2 (NCM) cathode active material. A laboratory-scale dispersing device was compared with a discontinuously working laboratory kneader and a continuously working extruder, both using 50% less solvent than the dissolver process. Rheological, mechanical, structural, conductive, imaging, and electrochemical analyses (C-rate test, long-term cycling) were carried out. The dispersing method and time were found to have a considerable impact on the structure and electrochemical performance. The continuous extrusion process resulted in good performance with more than 20% higher specific capacity at elevated C-rates compared with the discontinuous process. This can be attributed to better deagglomeration of the carbon black in the slurries, also resulting in 60% higher electrode conductivity. On top of these positive results, the changes in the drying step due to the reduced solvent use led to a 50% decrease in the time required for the constant-drying-rate period. The continuously working extrusion process was found to be most suitable for large-scale, cost-efficient, environmentally friendly production of slurries for lithium-ion battery electrodes.

  20. High-performance electrode materials of hierarchical mesoporous nickel oxide ultrathin nanosheets derived from self-assembled scroll-like α-nickel hydroxide

    NASA Astrophysics Data System (ADS)

    Yao, Mingming; Hu, Zhonghua; Xu, Zijie; Liu, Yafei; Liu, Peipei; Zhang, Qiang

    2015-01-01

    A two-step approach is proposed to prepare high-performance NiO electrode material. First, the scroll-like α-Ni(OH)2 is prepared by hydrothermal reaction via a self-assembly growth process using guanidine hydrochloride as precipitant. Second, the precursor Ni(OH)2 is converted to NiO by calcination. The resultants of hierarchical mesoporous NiO ultrathin nanosheets are characterized by X-ray diffraction (XRD), field-emission scanning electron microscopy (FESEM), transmission electron microscopy (TEM), selected area electron diffraction (SAED) patterns and N2 adsorption and desorption. The electrochemical properties of the samples are evaluated though cyclic voltammetry (CV), charge-discharge and electrochemical impedance spectroscopy (EIS) in 6.0 M KOH electrolytic solution. The results show that the typical hierarchical mesoporous NiO ultrathin nanosheets exhibits a very large specific capacitance of 1060 F g-1 at 1 A g-1, an outstanding cyclic stability with a capacitance retention of 91% after 5000 cycles of charge-discharge and a low resistance.

  1. High Performance Nickel Electrodes for Space Power Applications

    NASA Technical Reports Server (NTRS)

    Adanuvor, Prosper K.; Pearson, Johnnie A.; Miller, Brian; Tatarchuk, Bruce; Britton, Doris L.

    1996-01-01

    Performance characteristics such as efficiency, specific energy density and power density of nickel electrodes are generally limited by the electrode microstructure and nature of the active material within the electrode matrix. Progress is being made in our laboratory in a collaborative effort with NASA-Lewis Research Center to develop lighter weight, mechanically stable and highly efficient nickel electrodes for aerospace applications. Our approach is based on an electrode microstructure fabricated from a mixture of nickel fibers as small as 2 microns diameter and cellulose fibers. Performance data in flooded cell tests and cycle life data are presented. Performance characteristics are compared to other electrode microstructures such as the Fibrex Fiber mat and the Fibrex Powder substrate. The flexibility of our electrode microstructure and the significant advantages it offers in terms of weight and performance are demonstrated, in particular, its ability to accept charge at high rates and to discharge at high rates.

  2. Raman structural studies of the nickel electrode

    NASA Technical Reports Server (NTRS)

    Cornilsen, B. C.

    1985-01-01

    Raman spectroscopy is sensitive to empirically controlled nickel electrode structural variations, and has unique potential for structural characterization of these materials. How the structure relates to electrochemical properties is examined so that the latter can be more completely understood, controlled, and optimized. Electrodes were impregnated and cycled, and cyclic voltammetry is being used for electrochemical characterization. Structural variation was observed which has escaped detection using other methods. Structural changes are induced by: (1) cobalt doping, (2) the state of change or discharge, (3) the preparation conditions and type of buffer used, and (4) the formation process. Charged active mass has an NiOOH-type structure, agreeing with X-ray diffraction results. Discharged active mass, however, is not isostructural with beta-Ni(OH)2. Chemically prepared alpha phases are not isostructural either. A disordered structural model, containing point defects, is proposed for the cycled materials. This model explains K(+) incorporation. Band assignments were made and spectra interpreted for beta-Ni(OH)2, electrochemical NiOOH and chemically precipitated NiOOH.

  3. One-step solution combustion synthesis of cobalt-nickel oxides/C/Ni/CNTs nanocomposites as electrochemical capacitors electrode materials

    NASA Astrophysics Data System (ADS)

    Kang, Litao; Deng, Jiachun; Liu, Tiejun; Cui, Mangwei; Zhang, Xinyu; Li, Peiyang; Li, Ying; Liu, Xuguang; Liang, Wei

    2015-02-01

    With Co(NO3)2·6H2O (oxidizer and Co source), Ni(NO3)2·6H2O (oxidizer and Ni source) and citric acid (fuel) as starting materials, cobalt-nickel oxides/C/Ni ternary nanocomposites have been synthesized by a scalable, one-step solution combustion process at only 300 °C within 30 min in air. In these composites, the metallic nickel and amorphous carbon (conductive phases) were in situ formed by the reduction of Ni2+ and carbonization of the excess citric acid during combustion, respectively. Experimental results indicated that the fuel:oxidant and Co:Ni molar ratios in precursor solution showed strong influences on the phase composition, morphology and electrochemical performance of products. With the increase of the fuel dosage, the products transformed from well-crystallized cubic NiO/Ni to Ni (nickel-related phases), then to relatively amorphous Ni/NiO and finally NiO. Electrochemical tests indicated that the optimized product showed a high specific capacitance of 446 F g-1 at 1 A g-1 (or 280 F g-1 at 10 A g-1) with a Co:Ni:C6H8O7 molar ratio of 4:5:86/9. Significantly, besides its mild experimental conditions, the method could be used to prepare cobalt-nickel oxides/C/Ni/CNTs quarternary nanocomposites by simply adding acid-treated CNTs into precursor combustion solution. Thanks to the high electrical conduction of CNTs, the specific capacitance could be further improved up to 579 F g-1 at 1 A g-1, or 350 F g-1 at 10 A g-1.

  4. Development of a Micro-Fiber Nickel Electrode for Nickel-Hydrogen Cell

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1996-01-01

    The development of a high specific energy battery is one of the objectives of the lightweight nickel-hydrogen (NiH2) program at the NASA Lewis Research Center. The approach has been to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen fuel cell. Small fiber diameter nickel plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products and have an advantage of increased surface area available for the deposition of active materials. Initial tests include activation and capacity measurements at different discharge levels followed by half-cell cycle testing at 80 percent depth-of-discharge in a low Earth orbit regime. The electrodes that pass the initial tests are life cycle tested in a boiler plate nickel-hydrogen cell before flightweight designs are built and tested.

  5. Development of a Micro-Fiber Nickel Electrode for Nickel-Hydrogen Cell

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1996-01-01

    The development of a high specific energy battery is one of the objectives of the lightweight nickel-hydrogen (NiH2) program at the NASA Lewis Research Center. The approach has been to improve the nickel electrode by continuing combined in-house and contract efforts to develop a more efficient and lighter weight electrode for the nickel-hydrogen fuel cell. Small fiber diameter nickel plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products and have an advantage of increased surface area available for the deposition of active materials. Initial tests include activation and capacity measurements at different discharge levels followed by half-cell cycle testing at 80 percent depth-of-discharge in a low Earth orbit regime. The electrodes that pass the initial tests are life cycle tested in a boiler plate nickel-hydrogen cell before flightweight designs are built and tested.

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

    NASA Technical Reports Server (NTRS)

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

    1987-01-01

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

  7. 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.

  8. On the performance of stabilized α-nickel hydroxide as a nickel-positive electrode in alkaline storage batteries

    NASA Astrophysics Data System (ADS)

    Ganesh Kumar, V.; Munichandraiah, N.; Vishnu Kamath, P.; Shukla, A. K.

    The internal resistance of a stabilized α-nickel hydroxide electrode is found to be lower than that of a β-nickel hydroxide electrode as shown from studies of the open-circuit potential-time transients at all states-of-charge. Nevertheless, the self-discharge rates of the former is higher. Gasometric studies reveal that the charging efficiency of the α-nickel hydroxide electrode is higher than that of the β-nickel hydroxide electrode.

  9. Analysis of polyaniline-based nickel electrodes for electrochemical supercapacitors

    NASA Astrophysics Data System (ADS)

    Girija, T. C.; Sangaranarayanan, M. V.

    Polyaniline is deposited potentiodynamically on a nickel substrate in the presence of p-toluene sulfonic acid and the specific capacitance is estimated. The electrochemical characterisation of the electrode is carried out by means of cyclic voltammetry, electrochemical impedance spectroscopy, and galvanostatic charge-discharge experiments. The specific capacitance is ∼4.05 × 10 2 F g -1. This indicates the feasibility of the polyaniline-coated nickel electrode for use in electrochemical supercapacitors.

  10. Platinum Nickel Nanowires as Methanol Oxidation Electrocatalysts

    DOE PAGES

    Alia, Shaun M.; Pylypenko, Svitlana; Neyerlin, Kenneth C.; ...

    2015-08-27

    We investigated platinum(Pt) nickel (Ni) nanowires (PtNiNWs) as methanol oxidation reaction (MOR) catalysts in rotating disk electrode (RDE) half-cells under acidic conditions. Pt-ruthenium (Ru) nanoparticles have long been the state of the art MOR catalyst for direct methanol fuel cells (DMFCs) where Ru provides oxophilic sites, lowering the potential for carbon monoxide oxidation and the MOR onset. Ru, however, is a precious metal that has long term durability concerns. Ni/Ni oxide species offer a potential to replace Ru in MOR electrocatalysis. PtNiNWs were investigated for MOR and oxygen annealing was investigated as a route to improve catalyst performance (mass activitymore » 65% greater) and stability to potential cycling. Our results presented show that PtNiNWs offer significant promise in the area, but also result in Ni ion leaching that is a concern requiring further evaluation in fuel cells.« less

  11. Platinum Nickel Nanowires as Methanol Oxidation Electrocatalysts

    SciTech Connect

    Alia, Shaun M.; Pylypenko, Svitlana; Neyerlin, Kenneth C.; Kocha, Shyam S.; Pivovar, Bryan S.

    2015-08-27

    We investigated platinum(Pt) nickel (Ni) nanowires (PtNiNWs) as methanol oxidation reaction (MOR) catalysts in rotating disk electrode (RDE) half-cells under acidic conditions. Pt-ruthenium (Ru) nanoparticles have long been the state of the art MOR catalyst for direct methanol fuel cells (DMFCs) where Ru provides oxophilic sites, lowering the potential for carbon monoxide oxidation and the MOR onset. Ru, however, is a precious metal that has long term durability concerns. Ni/Ni oxide species offer a potential to replace Ru in MOR electrocatalysis. PtNiNWs were investigated for MOR and oxygen annealing was investigated as a route to improve catalyst performance (mass activity 65% greater) and stability to potential cycling. Our results presented show that PtNiNWs offer significant promise in the area, but also result in Ni ion leaching that is a concern requiring further evaluation in fuel cells.

  12. Sintered electrode for solid oxide fuel cells

    DOEpatents

    Ruka, R.J.; Warner, K.A.

    1999-06-01

    A solid oxide fuel cell fuel electrode is produced by a sintering process. An underlayer is applied to the electrolyte of a solid oxide fuel cell in the form of a slurry, which is then dried. An overlayer is applied to the underlayer and then dried. The dried underlayer and overlayer are then sintered to form a fuel electrode. Both the underlayer and the overlayer comprise a combination of electrode metal such as nickel, and stabilized zirconia such as yttria-stabilized zirconia, with the overlayer comprising a greater percentage of electrode metal. The use of more stabilized zirconia in the underlayer provides good adhesion to the electrolyte of the fuel cell, while the use of more electrode metal in the overlayer provides good electrical conductivity. The sintered fuel electrode is less expensive to produce compared with conventional electrodes made by electrochemical vapor deposition processes. The sintered electrodes exhibit favorable performance characteristics, including good porosity, adhesion, electrical conductivity and freedom from degradation. 4 figs.

  13. Flight Weight Design Nickel-Hydrogen Cells Using Lightweight Nickel Fiber Electrodes

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.; Willis, Bob; Pickett, David F.

    2003-01-01

    The goal of this program is to develop a lightweight nickel electrode for advanced aerospace nickel-hydrogen cells and batteries with improved specific energy and specific volume. The lightweight nickel electrode will improve the specific energy of a nickel-hydrogen cell by >50%. These near-term advanced batteries will reduce power system mass and volume, while decreasing the cost, thus increasing mission capabilities and enabling small spacecraft missions. This development also offers a cost savings over the traditional sinter development methods for fabrication. The technology has been transferred to Eagle-Picher, a major aerospace battery manufacturer, who has scaled up the process developed at NASA GRC and fabricated electrodes for incorporation into flight-weight nickel-hydrogen cells.

  14. Flight Weight Design Nickel-Hydrogen Cells Using Lightweight Nickel Fiber Electrodes

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.; Willis, Bob; Pickett, David F.

    2003-01-01

    The goal of this program is to develop a lightweight nickel electrode for advanced aerospace nickel-hydrogen cells and batteries with improved specific energy and specific volume. The lightweight nickel electrode will improve the specific energy of a nickel-hydrogen cell by >50%. These near-term advanced batteries will reduce power system mass and volume, while decreasing the cost, thus increasing mission capabilities and enabling small spacecraft missions. This development also offers a cost savings over the traditional sinter development methods for fabrication. The technology has been transferred to Eagle-Picher, a major aerospace battery manufacturer, who has scaled up the process developed at NASA GRC and fabricated electrodes for incorporation into flight-weight nickel-hydrogen cells.

  15. Electrochemical impregnation of nickel hydroxide in porous electrodes

    NASA Technical Reports Server (NTRS)

    Ho, Kuo-Chuan; Jorne, Jacob

    1987-01-01

    The electrochemical impregnation of nickel hydroxide in porous electrode was investigated both experimentally and theoretically. The loading level and plaque expansion were the most important parameters to be considered. The effects of applied current density, stirring, ratio of solution to electrode volume and pH were identified. A novel flow through electrochemical impregnation is proposed in which the electrolyte is forced through the porous nickel plaque. The thickening of the plaque can be reduced while maintaining high loading capacity. A mathematical model is presented which describes the transport of the nitrate, nickel and hydroxyl ions and the consecutive heterogeneous electrochemical reduction of nitrate and the homogeneous precipitation reaction of nickel hydroxide. The distributions of precipitation rate and active material within the porous electrode are obtained. A semiempirical model is also proposed which takes into account the plugging of the pores.

  16. Nickel inhibits mitochondrial fatty acid oxidation.

    PubMed

    Uppala, Radha; McKinney, Richard W; Brant, Kelly A; Fabisiak, James P; Goetzman, Eric S

    2015-08-07

    Nickel exposure is associated with changes in cellular energy metabolism which may contribute to its carcinogenic properties. Here, we demonstrate that nickel strongly represses mitochondrial fatty acid oxidation-the pathway by which fatty acids are catabolized for energy-in both primary human lung fibroblasts and mouse embryonic fibroblasts. At the concentrations used, nickel suppresses fatty acid oxidation without globally suppressing mitochondrial function as evidenced by increased glucose oxidation to CO2. Pre-treatment with l-carnitine, previously shown to prevent nickel-induced mitochondrial dysfunction in neuroblastoma cells, did not prevent the inhibition of fatty acid oxidation. The effect of nickel on fatty acid oxidation occurred only with prolonged exposure (>5 h), suggesting that direct inhibition of the active sites of metabolic enzymes is not the mechanism of action. Nickel is a known hypoxia-mimetic that activates hypoxia inducible factor-1α (HIF1α). Nickel-induced inhibition of fatty acid oxidation was blunted in HIF1α knockout fibroblasts, implicating HIF1α as one contributor to the mechanism. Additionally, nickel down-regulated the protein levels of the key fatty acid oxidation enzyme very long-chain acyl-CoA dehydrogenase (VLCAD) in a dose-dependent fashion. In conclusion, inhibition of fatty acid oxidation by nickel, concurrent with increased glucose metabolism, represents a form of metabolic reprogramming that may contribute to nickel-induced carcinogenesis.

  17. Modified cermet fuel electrodes for solid oxide electrochemical cells

    DOEpatents

    Ruka, Roswell J.; Spengler, Charles J.

    1991-01-01

    An exterior porous electrode (10), bonded to a solid oxygen ion conducting electrolyte (13) which is in contact with an interior electrode (14), contains coarse metal particles (12) of nickel and/or cobalt, having diameters from 3 micrometers to 35 micrometers, where the coarse particles are coated with a separate, porous, multiphase layer (17) containing fine metal particles of nickel and/or cobalt (18), having diameters from 0.05 micrometers to 1.75 micrometers and conductive oxide (19) selected from cerium oxide, doped cerium oxide, strontium titanate, doped strontium titanate and mixtures thereof.

  18. Nickel Inhibits Mitochondrial Fatty Acid Oxidation

    PubMed Central

    Uppala, Radha; McKinney, Richard W.; Brant, Kelly A.; Fabisiak, James P.; Goetzman, Eric S.

    2015-01-01

    Nickel exposure is associated with changes in cellular energy metabolism which may contribute to its carcinogenic properties. Here, we demonstrate that nickel strongly represses mitochondrial fatty acid oxidation—the pathway by which fatty acids are catabolized for energy—in both primary human lung fibroblasts and mouse embryonic fibroblasts. At the concentrations used, nickel suppresses fatty acid oxidation without globally suppressing mitochondrial function as evidenced by increased glucose oxidation to CO2. Pre-treatment with L-carnitine, previously shown to prevent nickel-induced mitochondrial dysfunction in neuroblastoma cells, did not prevent the inhibition of fatty acid oxidation. The effect of nickel on fatty acid oxidation occurred only with prolonged exposure (>5 hr), suggesting that direct inhibition of the active sites of metabolic enzymes is not the mechanism of action. Nickel is a known hypoxia-mimetic that activates hypoxia inducible factor-1α (HIF1α). Nickel-induced inhibition of fatty acid oxidation was blunted in HIF1α knockout fibroblasts, implicating HIF1α as one contributor to the mechanism. Additionally, nickel down-regulated the protein levels of the key fatty acid oxidation enzyme very long-chain acyl-CoA dehydrogenase (VLCAD) in a dose-dependent fashion. In conclusion, inhibition of fatty acid oxidation by nickel, concurrent with increased glucose metabolism, represents a form of metabolic reprogramming that may contribute to nickel-induced carcinogenesis. PMID:26051273

  19. Long life nickel electrodes for a nickel-hydrogen cell: Cycle life tests

    NASA Technical Reports Server (NTRS)

    Lim, H. S.; Verzwyvelt, S. A.

    1985-01-01

    In order to develop a long life nickel electrode for a Ni/H2 cell, the cycle life of nickel electrodes was tested in Ni/H2 boiler plate cells. A 19 test cell matrix was made of various nickel electrode designs including three levels each of plaque mechanical strength, median pore size of the plaque, and active material loading. Test cells were cycled to the end of their life (0.5v) in a 45 minute low Earth orbit cycle regime at 80% depth-of-discharge. It is shown that the active material loading level affects the cycle life the most with the optimum loading at 1.6 g/cc void. Mechanical strength does not affect the cycle life noticeably in the bend strength range of 400 to 700 psi. It is found that the best plaque is made of INCO nickel powder type 287 and has median pore size of 13 micron.

  20. Advanced catalytic electrode development for nickel-hydrogen batteries

    SciTech Connect

    Coates, D.K.; Grindstaff, B.K.; Hoofnagle, P.S.; Chiappetti, D.P.

    1995-12-31

    Low catalyst loading gas diffusion membrane electrodes have been developed for spaceflight qualified nickel-hydrogen (NiH{sub 2}) batteries. These electrodes involve the use of new electrode designs and innovative manufacturing methods. Supported catalysts, mixed catalysts and alterative catalyst systems have been developed to decrease catalyst loading levels, and therefore reduce electrode cost, without reducing performance or reliability. This advanced electrode technology has currently accumulated more than 13,000 charge/discharge cycles in real-time, low-earth-orbit (LEO) testing. The technology has been incorporated into several nickel-hydrogen spaceflight programs including the TUBSAT B spacecraft, built by the Technical University of Berlin and launched in January of 1994 aboard a Russian Cyclone rocket.

  1. Investigation of optical properties of nickel oxide thin films deposited on different substrates

    NASA Astrophysics Data System (ADS)

    Nama Manjunatha, Krishna; Paul, Shashi

    2015-10-01

    Nickel oxide has been investigated for several potential applications, namely, ultraviolet detectors, electro chromic devices, displays, diodes for light emitting, transparent conductive electrode, and optoelectronic devices. These applications require an in depth analysis of nickel oxide prior to its exploration in aforementioned devices. Optical properties of materials were investigated by depositing thin film of nickel oxide on different substrates in order to understand if the choice of substrate can have effect on deducing various optical parameters and can lead to wrong conclusions. In view of this, we have investigated optical properties of nickel oxide deposited on different substrates (glass, transparent plastic, sapphire, potassium bromide, and calcium fluoride).

  2. Electroanalysis of tetracycline using nickel-implanted boron-doped diamond thin film electrode applied to flow injection system.

    PubMed

    Treetepvijit, Surudee; Chuanuwatanakul, Suchada; Einaga, Yasuaki; Sato, Rika; Chailapakult, Orawon

    2005-05-01

    The electrochemical analysis of tetracycline was investigated using nickel-implanted boron-doped diamond thin film electrode by cyclic voltammetry and amperometry with a flow injection system. Cyclic voltammetry was used to study the electrochemical oxidation of tetracycline. Comparison experiments were carried out using as-deposited boron-doped diamond thin film electrode (BDD). Nickel-implanted boron-doped diamond thin film electrode (Ni-DIA) provided well-resolved oxidation irreversible cyclic voltammograms. The current signals were higher than those obtained using the as-deposited BDD electrode. Results using nickel-implanted boron-doped diamond thin film electrode in flow injection system coupled with amperometric detection are presented. The optimum potential for tetracycline was 1.55 V versus Ag/AgCl. The linear range of 1.0 to 100 microM and the detection limit of 10 nM were obtained. In addition, the application for drug formulation was also investigated.

  3. Positive electrodes of nickel-cadmium batteries

    NASA Technical Reports Server (NTRS)

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

    1985-01-01

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

  4. Porous Nickel Oxide Film Sensor for Formaldehyde

    NASA Astrophysics Data System (ADS)

    Cindemir, U.; Topalian, Z.; Österlund, L.; Granqvist, C. G.; Niklasson, G. A.

    2014-11-01

    Formaldehyde is a volatile organic compound and a harmful indoor pollutant contributing to the "sick building syndrome". We used advanced gas deposition to fabricate highly porous nickel oxide (NiO) thin films for formaldehyde sensing. The films were deposited on Al2O3 substrates with prefabricated comb-structured electrodes and a resistive heater at the opposite face. The morphology and structure of the films were investigated with scanning electron microscopy and X-ray diffraction. Porosity was determined by nitrogen adsorption isotherms with the Brunauer-Emmett-Teller method. Gas sensing measurements were performed to demonstrate the resistive response of the sensors with respect to different concentrations of formaldehyde at 150 °C.

  5. CHROMIUM ELECTROANALYSIS AT SCREEN PRINTED ELECTRODE MODIFIED BY THIN FILMS OF NICKEL

    EPA Science Inventory

    A rapid and potentially cost-effective electrochemical method is reported for analysis of chromium (VI) and Chromium(III) using a nickel modified screen printed carbon ink electrode. Electrochemical characteristics of nickel modified electrode as well voltammetric behavior f...

  6. CHROMIUM ELECTROANALYSIS AT SCREEN PRINTED ELECTRODE MODIFIED BY THIN FILMS OF NICKEL

    EPA Science Inventory

    A rapid and potentially cost-effective electrochemical method is reported for analysis of chromium (VI) and Chromium(III) using a nickel modified screen printed carbon ink electrode. Electrochemical characteristics of nickel modified electrode as well voltammetric behavior f...

  7. Combination nickel foam expanded nickel screen electrical connection supports for solid oxide fuel cells

    DOEpatents

    Draper, Robert; Prevish, Thomas; Bronson, Angela; George, Raymond A.

    2007-01-02

    A solid oxide fuel assembly is made, wherein rows (14, 25) of fuel cells (17, 19, 21, 27, 29, 31), each having an outer interconnection (20) and an outer electrode (32), are disposed next to each other with corrugated, electrically conducting expanded metal mesh member (22) between each row of cells, the corrugated mesh (22) having top crown portions and bottom portions, where the top crown portion (40) have a top bonded open cell nickel foam (51) which contacts outer interconnections (20) of the fuel cells, said mesh and nickel foam electrically connecting each row of fuel cells, and where there are no more metal felt connections between any fuel cells.

  8. Progress in the Development of Lightweight Nickel Electrode for Nickel-Hydrogen Cell

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1999-01-01

    Development of a high specific energy battery is one of the objectives of the lightweight nickel-hydrogen (Ni-H2) program at the NASA Glenn Research Center. The approach has been to improve the nickel electrode by continuing combined in-house and contract efforts to develop a lighter weight electrode for the nickel-hydrogen cell. Small fiber diameter nickel plaques are used as conductive supports for the nickel hydroxide active material. These plaques are commercial products and have an advantage of increased surface area available for the deposition of active material. Initial tests include activation and capacity measurements at five different discharge levels, C/2, 1.0 C, 1.37 C, 2.0 C, and 2.74 C. The electrodes are life cycle tested using a half-cell configuration at 40 and 80% depths-of-discharge (DOD) in a low-Earth-orbit regime. The electrodes that pass the initial tests are life cycle-tested in a boiler plate nickel-hydrogen cell before flight weight design are built and tested.

  9. Contribution to the knowledge of nickel hydroxide electrodes. 5. Analysis and electrochemical behavior of cadmium nickel hydroxides

    NASA Technical Reports Server (NTRS)

    Bode, H.; Dennstedt, W.

    1981-01-01

    Electrochemical experiments performed at sintered and bulk electrodes show that beta nickel hydroxide contains an electrochemically inactive proportion of cadmium hydroxide of up to 10%. The electrochemically ineffective cadmium hydroxide is homogeneously dissolved in beta nickel hydroxide.

  10. Characterization of cobalt-dipped nickel electrodes with fibrex substrates

    NASA Technical Reports Server (NTRS)

    Youngman, Carolyn A.; Reid, Margaret A.

    1995-01-01

    Nickel electrodes using fibrous substrates have poorer initial utilization of the active material than those using conventional nickel sinter substrates. Previous investigators had shown that utilization can be dramatically improved by dipping these electrodes in a cobalt solution immediately after the electrochemical impregnation, before formation and cycling is carried out. The present study looked at the gas evolution behavior of dipped and undipped electrodes, impedance curves, and the charge-discharge curves to try to understand the reasons for the improvement in utilization. Impedance measurements under open circuit conditions indicate that some of the improvement is due to a reduction in the ohmic resistance of the surface layer of the particles, in agreement with earlier work. The charge-discharge curves suggest that there may also be an additional increase in the ohmic resistance of the surface layer of the undipped electrode during charging.

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

    NASA Technical Reports Server (NTRS)

    Luksha, E.; Gordy, D. J.

    1972-01-01

    Supposedly long-lived nickel-cadmium batteries often fail due to severe gassing on charge. In order to increase the lives of such cells attempts are being made to construct nongassing positive and negative electrodes. The gassing characteristics of both electrodes in negative limited cells were determined as a function of charge rate, charge temperature, and loading. Cycle life tests, up to 70 cycles, of some of the cells show they operate in a nongassing manner with very low degradation rates.

  12. One-step solvothermal tailoring the compositions and phases of nickel cobalt sulfides on conducting oxide substrates as counter electrodes for efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Huang, Niu; Li, Guowang; Huang, Hua; Sun, Panpan; Xiong, Tianli; Xia, Zhifen; Zheng, Fang; Xu, Jixing; Sun, Xiaohua

    2016-12-01

    Several nickel cobalt sulfide (Ni-Co-S) counter electrodes (CEs) are prepared, and the Ni-Co-S nanoparticles are in-situ grown on SnO2: F (FTO) transparent conductive glasses via a facile solvothermal process, in which thiourea is used as the sulfurizing reagent. The X-ray diffraction, scanning electron microscopy, and energy dispersive spectrometer are employed to measure the microstructure and composition of the Ni-Co-S CEs. When a proper amount of thiourea is adopted, fine crystalline NiCo2S4 CE is obtained. When the amount of thiourea is small or large, (Ni,Co)4S3 or (Ni,Co)3S4 CE is acquired, respectively. Cyclic voltammetry, electrochemical impedance spectroscopy, Tafel polarization and open-circuit voltage decay (OCVD) measurements all demonstrate that the electrocatalytic activities and electrical conductivities of these Ni-Co-S CEs all approach or exceed those of Pt-pyrolysis CE. Their superior electrochemical performances are further confirmed by fabricating DSSCs with the Ni-Co-S CEs, they display similar or better photo-electric conversion efficiencies to/than the Pt-pyrolysis counterpart.

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

    NASA Technical Reports Server (NTRS)

    Luksha, E.; Gordy, D. J.

    1972-01-01

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

  14. One-Step In Situ Growth of Iron-Nickel Sulfide Nanosheets on FeNi Alloy Foils: High-Performance and Self-Supported Electrodes for Water Oxidation.

    PubMed

    Yuan, Cheng-Zong; Sun, Zhong-Ti; Jiang, Yi-Fan; Yang, Zheng-Kun; Jiang, Nan; Zhao, Zhi-Wei; Qazi, Umair Yaqub; Zhang, Wen-Hua; Xu, An-Wu

    2017-05-01

    Efficient and durable oxygen evolution reaction (OER) catalysts are highly required for the cost-effective generation of clean energy from water splitting. For the first time, an integrated OER electrode based on one-step direct growth of metallic iron-nickel sulfide nanosheets on FeNi alloy foils (denoted as FeNi3 S2 /FeNi) is reported, and the origin of the enhanced OER activity is uncovered in combination with theoretical and experimental studies. The obtained FeNi3 S2 /FeNi electrode exhibits highly catalytic activity and long-term stability toward OER in strong alkaline solution, with a low overpotential of 282 mV at 10 mA cm(-2) and a small Tafel slope of 54 mV dec(-1) . The excellent activity and satisfactory stability suggest that the as-made electrode provides an attractive alternative to noble metal-based catalysts. Combined with density functional theory calculations, exceptional OER performance of FeNi3 S2 /FeNi results from a combination of efficient electron transfer properties, more active sites, the suitable O2 evolution kinetics and energetics benefited from Fe doping. This work not only simply constructs an excellent electrode for water oxidation, but also provides a deep understanding of the underlying nature of the enhanced OER performance, which may serve as a guide to develop highly effective and integrated OER electrodes for water splitting. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Anodic stripping voltammetry of nickel ions and nickel hydroxide nanoparticles at boron-doped diamond electrodes

    NASA Astrophysics Data System (ADS)

    Musyarofah, N. R. R.; Gunlazuardi, J.; Einaga, Y.; Ivandini, T. A.

    2017-04-01

    Anodic stripping voltammetry (ASV) of nickel ions in phosphate buffer solution (PBS) have been investigated at boron-doped diamond (BDD) electrodes. The deposition potential at 0.1 V (vs. Ag/AgCl) for 300 s in 0.1 M PBS pH 3 was found as the optimum condition. The condition was applied for the determination of nickel contained in nickel hydroxide nanoparticles. A linear calibration curve can be achieved of Ni(OH)2-NPs in the concentration range of x to x mM with an estimated limit of detection (LOD) of 5.73 × 10-6 mol/L.

  16. Nickel exposure and plasma levels of biomarkers for assessing oxidative stress in nickel electroplating workers.

    PubMed

    Tsao, Yu-Chung; Gu, Po-Wen; Liu, Su-Hsun; Tzeng, I-Shiang; Chen, Jau-Yuan; Luo, Jiin-Chyuan John

    2017-07-01

    The mechanism of nickel-induced pathogenesis remains elusive. To examine effects of nickel exposure on plasma oxidative and anti-oxidative biomarkers. Biomarker data were collected from 154 workers with various levels of nickel exposure and from 73 controls. Correlations between nickel exposure and oxidative and anti-oxidative biomarkers were determined using linear regression models. Workers with a exposure to high nickel levels had significantly lower levels of anti-oxidants (glutathione and catalase) than those with a lower exposure to nickel; however, only glutathione showed an independent association after multivariable adjustment. Exposure to high levels of nickel may reduce serum anti-oxidative capacity.

  17. Electrophoretic self-assembly of expanded mesocarbon microbeads with attached nickel nanoparticles as a high-rate electrode for supercapacitors.

    PubMed

    Wu, Mao-Sung; Fu, Yan-Hao

    2014-04-21

    Expanded mesocarbon microbeads (EMCMBs) with graphene oxide (GO) sheets were prepared by expanding graphitized mesocarbon microbeads (MCMBs) using a simple solution-based oxidative process. EMCMB-supported nickel nanoparticles with an average size of 4.6 nm were fabricated by an electrophoretic deposition (EPD) method in the presence of nickel nitrate additive. Nickel ions were self-assembled on the fluffy GO sheets resulting in a more positively charged EMCMB particle for facilitating EPD and dispersion. After heat treatment at 300 °C, GO could be converted to graphene which could provide a conductive network for facilitating the transport of electrons. Well-dispersed nickel nanoparticles on graphene sheets could act as a redox center to allow storage of extra charge and a nanospacer to prevent the graphene sheets from restacking. The specific capacitance of EMCMB-supported nickel electrode could reach 491 F g(-1), which is much higher than that of EMCMB electrode (43 F g(-1)) and bare nickel electrode (146 F g(-1)) at a discharge current of 5 A g(-1). More importantly, the EMCMB-supported nickel electrode is capable of delivering a high specific capacitance of 440 F g(-1) at a discharge current of 50 A g(-1), and could pave the way towards high-rate supercapacitors.

  18. A novel voltammetric sensor for amoxicillin based on nickel-curcumin complex modified carbon paste electrode.

    PubMed

    Ojani, Reza; Raoof, Jahan-Bakhsh; Zamani, Saeed

    2012-06-01

    The electrocatalytic oxidation of amoxicillin was investigated on a nickel-based (Ni(II)-curcumin) chemically modified electrode. This modified electrode was prepared by electropolymerization of complex (curcumin = 1,7-bis[4-hydroxyl-3-methoxyphenyl]-1,6-heptadiene-3,5-dione) in alkaline solution. For the first time, the catalytic oxidation of amoxicillin was demonstrated by cyclic voltammetry, chronoamperometry, chronocoulometry and amperometry methods at the surface of this modified carbon paste electrode. The obtained results showed that NiOOH acts as an electrocatalyst for oxidation of amoxicillin. This electrocatalytic oxidation exhibited a good linear response for amoxicillin concentration over the range of 8 × 10⁻⁶-1×10⁻⁴ M with a detection limit of 5 × 10⁻⁶ M. Therefore, this electrocatalytic method was used as a simple, selective and rapid method able to determine amoxicillin in pharmaceutical preparations and biological media.

  19. Synthese, etude structurale et electrochimique des materiaux d'electrode positive d'oxydes mixtes lithium cobalt nickel oxide (0 /= 1) pour les batteries rechargeables au lithium

    NASA Astrophysics Data System (ADS)

    Grincourt, Yves

    Depuis une dizaine d'annees, on observe un interet grandissant pour les batteries rechargeables au lithium de tension superieure a 4 volts. La commercialisation de ces batteries pour l'electronique grand marche tend de plus en plus a supplanter celle des accumulateurs Ni-Cd et Ni-MH, de tension nominate 1,2 V. Ces batteries au lithium font appel a des materiaux d'electrode positive (cathode a la decharge) du type oxydes mixtes de metaux de transition LiMnO 2, LiMn2O4, LiNiO2 ou LiCoO2. Si le compose LiCoO2 est relativement aise a synthetiser, il n'en demeure pas moins que le cobalt reste un metal plus couteux compare au nickel et au manganese. La synthese de LiNiO2, quart a elle, demeure un probleme du point de vue stoechiometrique. Un defaut de lithium (5 a 10% molaire) conduira a des proprietes electrochimiques mediocres de la batterie. Dans cette etude nous nous proposons donc de preparer par voie humide et par voie seche les materiaux d'electrode positive de la famille LiCoyNi1-yO2 aver (0 ≤ y ≤ 1) et d'etudier en detail l'influence du pourcentage de nickel et de cobalt sur les proprietes electrochimiques des oxydes mixtes Li-Ni-Co. Une des caracteristiques est la morphologie plus fine des poudres de materiaux, observes par microscopie electronique a balayage (MEB). Un traitement thermique a plus basse temperature (750°C) que pour LiCoO2 (850°C) ainsi qu'un leger exces de lithium dans la preparation, ont permis d'aboutir a un materiau de stoechiometrie quasi parfaite. Neanmoins, le role de pilfer joue par 2 a 4% de moles de Ni2+ presents sur les sites lithium, permet de conserver intacte la structure hexagonale de la maille entre deux cycles consecutifs. Afin de mieux comprendre l'influence du vieillissement dune demi-pile Li/LiMeO2 (Me = Ni, Co) a temperature ambiante, des etudes electrochimiques et d'impedance spectroscopique ont ete menees en parallele. Le vieillissement de la cellule s'accompagne seulement dune chute de son potentiel due a son auto

  20. Simultaneous voltammetric determination of dopamine and epinephrine in human body fluid samples using a glassy carbon electrode modified with nickel oxide nanoparticles and carbon nanotubes within a dihexadecylphosphate film.

    PubMed

    Figueiredo-Filho, Luiz C S; Silva, Tiago A; Vicentini, Fernando C; Fatibello-Filho, Orlando

    2014-06-07

    A simple and highly selective electrochemical method was developed for the single or simultaneous determination of dopamine (DA) and epinephrine (EP) in human body fluids using a glassy carbon electrode modified with nickel oxide nanoparticles and carbon nanotubes within a dihexadecylphosphate film using square-wave voltammetry (SWV) or differential-pulse voltammetry (DPV). Using DPV with the proposed electrode, a separation of ca. 360 mV between the peak reduction potentials of DA and EP present in binary mixtures was obtained. The analytical curves for the simultaneous determination of dopamine and epinephrine showed an excellent linear response, ranging from 7.0 × 10(-8) to 4.8 × 10(-6) and 3.0 × 10(-7) to 9.5 × 10(-6) mol L(-1) for DA and EP, respectively. The detection limits for the simultaneous determination of DA and EP were 5.0 × 10(-8) mol L(-1) and 8.2 × 10(-8) mol L(-1), respectively. The proposed method was successfully applied in the simultaneous determination of these analytes in human body fluid samples of cerebrospinal fluid, human serum and lung fluid.

  1. Screenable all-metal solar cell electrodes of nickel and copper

    NASA Technical Reports Server (NTRS)

    Ross, B.; Bickler, D. B.

    1981-01-01

    Screenable thick film solar cell electrodes are made using the all-metal electrode system, which eliminates the commonly used glass frit and substitutes an oxide scavenger such as silver fluoride. The low temperature firing copper metal systems give good results on solar cells obtaining cell efficiencies of 13% AM1, and adhering sintered structures are demonstrated with nickel systems. The potential effect of copper upon cell performance at elevated temperatures over long periods of time is determined, and it is found that the formation of a copper-silicon eutectic at 550 C produces needle-like structures with broad bases on the silicon, extending into and occasionally through the metallization layer.

  2. Recent Advances in the Synthesis and Stabilization of Nickel and Nickel Oxide Nanoparticles: A Green Adeptness.

    PubMed

    Imran Din, Muhammad; Rani, Aneela

    2016-01-01

    Green protocols for the synthesis of nanoparticles have been attracting a lot of attention because they are eco-friendly, rapid, and cost-effective. Nickel and nickel oxide nanoparticles have been synthesized by green routes and characterized for impact of green chemistry on the properties and biological effects of nanoparticles in the last five years. Green synthesis, properties, and applications of nickel and nickel oxide nanoparticles have been reported in the literature. This review summarizes the synthesis of nickel and nickel oxide nanoparticles using different biological systems. This review also provides comparative overview of influence of chemical synthesis and green synthesis on structural properties of nickel and nickel oxide nanoparticles and their biological behavior. It concludes that green methods for synthesis of nickel and nickel oxide nanoparticles are better than chemical synthetic methods.

  3. Recent Advances in the Synthesis and Stabilization of Nickel and Nickel Oxide Nanoparticles: A Green Adeptness

    PubMed Central

    Rani, Aneela

    2016-01-01

    Green protocols for the synthesis of nanoparticles have been attracting a lot of attention because they are eco-friendly, rapid, and cost-effective. Nickel and nickel oxide nanoparticles have been synthesized by green routes and characterized for impact of green chemistry on the properties and biological effects of nanoparticles in the last five years. Green synthesis, properties, and applications of nickel and nickel oxide nanoparticles have been reported in the literature. This review summarizes the synthesis of nickel and nickel oxide nanoparticles using different biological systems. This review also provides comparative overview of influence of chemical synthesis and green synthesis on structural properties of nickel and nickel oxide nanoparticles and their biological behavior. It concludes that green methods for synthesis of nickel and nickel oxide nanoparticles are better than chemical synthetic methods. PMID:27413375

  4. Long Life Nickel Electrodes for a Nickel-hydrogen Cell: Cycle Life Tests

    NASA Technical Reports Server (NTRS)

    Lim, H. S.; Verzwyvelt, S. A.

    1984-01-01

    In order to develop a long life nickel electrode for a Ni/H2 cell, cycle life tests of nickel electrodes were carried out in Hi/H2 boiler plate cells. A 19 test cell matrix was made of various nickel electrode designs including three levels each of plaque mechanical strength, median pore size of the plaque, and active material loading. Test cells were cycled to the end of their life (0.5v) in a 45-minute low earth orbit cycle regime at 80% depth-of-discharge. The results show that the active material loading level affects the cycle life the most with the optimum loading at 1.6 g/cc void. Mechanical strength did not affect the cycle life noticeably in the bend strength range of 400 to 700 psi. The best plaque type appears to be one which is made of INCO nickel powder type 287 and has a median pore size of 13 micron.

  5. A study of the electrochemistry of nickel hydroxide electrodes with various additives

    NASA Astrophysics Data System (ADS)

    Zhu, Wen-Hua; Ke, Jia-Jun; Yu, Hong-Mei; Zhang, Deng-Jun

    Nickel composite electrodes (NCE) with various additives are prepared by a chemical impregnation method from nitrate solutions on sintered porous plaques. The electrochemical properties, such as utilization of active material, swelling and the discharge potential of the nickel oxide electrode (NOE) are determined mainly through the composition of the active material and the characteristics of nickel plaques. Most additives (Mg, Ca, Sr, Ba, Zn, Cd, Co, Li and Al hydroxide) exert effects on the discharge potential and swelling of the NOE. Chemical co-precipitation with the addition of calcium, zinc, magnesium and barium hydroxide increases the discharge potential by more than 20 mV, but that with zinc hydroxide results in an obvious decrease of active-material utilization and that with calcium and magnesium hydroxide produces a larger increase of electrode thickness. The effects of anion additives are also examined. Less than 1% mol of NiS in the active material increases the discharge potential. Cadmium, cobalt and zinc hydroxide are excellent additives for preventing swelling of the NCE. Slow voltammetry (0.2 mV s -1) in 6 M KOH is applied to characterize the oxygen-evolving potential of the NCE. The difference between the oxygen-evolution potential and the potential of the oxidation peak for the NCE with additives of calcium, lithium, barium and aluminium hydroxide is at least + 60 mV.

  6. Nickel.

    PubMed

    Barceloux, D G

    1999-01-01

    Nickel is an essential element for at least several animal species. These animal studies associate nickel deprivation with depressed growth, reduced reproductive rates, and alterations of serum lipids and glucose. Although there is substantial evidence of an essential status for nickel in animals, a deficiency state in humans has not been clearly defined. Nickel is a silver-white metal with siderophilic properties that facilitate the formation of nickel-iron alloys. In contrast to the soluble nickel salts (chloride, nitrate, sulfate), metallic nickel, nickel sulfides, and nickel oxides are poorly water-soluble. Nickel carbonyl is a volatile liquid at room temperature that decomposes rapidly into carbon monoxide and nickel. Drinking water and food are the main sources of exposure for the general population with the average American diet containing about 300 micrograms Ni/d. Nickel is highly mobile in soil, particularly in acid soils. There is little evidence that nickel compounds accumulate in the food chain. Nickel is not a cumulative toxin in animals or in humans. Almost all cases of acute nickel toxicity result from exposure to nickel carbonyl. The initial effects involve irritation of the respiratory tract and nonspecific symptoms. Patients with severe poisoning develop intense pulmonary and gastrointestinal toxicity. Diffuse interstitial pneumonitis and cerebral edema are the main cause of death. Sodium diethyldithiocarbamate is an investigational drug used to chelate nickel following exposure to nickel carbonyl. Nickel is a common sensitizing agent with a high prevalence of allergic contact dermatitis. Nickel and nickel compounds are well-recognized carcinogens. However, the identity of the nickel compound or compounds, which cause the increased risk of cancer, remains unclear. Currently, there are little epidemiological data to indicate that exposure to metallic nickel increases the risk of cancer, or that exposure to the carcinogenic forms of nickel causes

  7. Nickel aluminides and nickel-iron aluminides for use in oxidizing environments

    DOEpatents

    Liu, Chain T.

    1988-03-15

    Nickel aluminides and nickel-iron aluminides treated with hafnium or zirconium, boron and cerium to which have been added chromium to significantly improve high temperature ductility, creep resistance and oxidation properties in oxidizing environments.

  8. Investigation of hydrogen evolution activity for the nickel, nickel-molybdenum nickel-graphite composite and nickel-reduced graphene oxide composite coatings

    NASA Astrophysics Data System (ADS)

    Jinlong, Lv; Tongxiang, Liang; Chen, Wang

    2016-03-01

    The nickel, nickel-molybdenum alloy, nickel-graphite and nickel-reduced graphene oxide composite coatings were obtained by the electrodeposition technique from a nickel sulfate bath. Nanocrystalline molybdenum, graphite and reduced graphene oxide in nickel coatings promoted hydrogen evolution reaction in 0.5 M H2SO4 solution at room temperature. However, the nickel-reduced graphene oxide composite coating exhibited the highest electrocatalytic activity for the hydrogen evolution reaction in 0.5 M H2SO4 solution at room temperature. A large number of gaps between 'cauliflower' like grains could decrease effective area for hydrogen evolution reaction in slight amorphous nickel-molybdenum alloy. The synergistic effect between nickel and reduced graphene oxide promoted hydrogen evolution, moreover, refined grain in nickel-reduced graphene oxide composite coating and large specific surface of reduced graphene oxide also facilitated hydrogen evolution reaction.

  9. Three-dimensional nickel foam/graphene/NiCo2O4 as high-performance electrodes for supercapacitors

    NASA Astrophysics Data System (ADS)

    Nguyen, Van Hoa; Shim, Jae-Jin

    2015-01-01

    A facile and efficient two-step method for the decoration of graphene sheets and nickel cobalt oxide (NiCo2O4) nanoparticles on conducting nickel foam was developed. First, graphene and a bimetallic (Ni, Co) hydroxide precursor were deposited on a Ni foam support by electrodeposition followed by a thermal transformation of the bimetallic hydroxide to NiCo2O4. The graphene layer with a thickness of a few nanometers was decorated with NiCo2O4 nanoparticles, ranging in size from 3 to 5 nm. The nickel foam electrode supported graphene and NiCo2O4 exhibited rapid electron and ion transport, large electroactive surface area, and excellent structural stability. The specific capacitance of the obtained electrode was as high as 1950 F g-1 at a high current density of 7.5 A g-1, suggesting its promising applications as an efficient electrode for electrochemical capacitors.

  10. Nanoporous nickel microspheres: synthesis and application for the electrocatalytic oxidation and determination of acyclovir.

    PubMed

    Heli, Hossein; Pourbahman, Fatemeh; Sattarahmady, Naghmeh

    2012-01-01

    Nickel microspheres were synthesized via a water-in-oil reverse nanoemulsion system using nickel nitrate as the nickel precursor and hydrazine hydrate as the reducing agent. The nanoemulsion was a triton X-100/cyclohexane/water ternary system. The surface morphology of the nickel microspheres was studied by scanning electron microscopy, which indicated that the microspheres had a nanoporous structure. The electrochemical behavior of the nanoporous nickel microspheres were studied in alkaline solution and were then employed to fabricate a modified carbon paste electrode in order to investigate the electrocatalytic oxidation of the drug acyclovir. The oxidation process involved, and its kinetics were investigated using cyclic voltammetry and chronoamperometry. The rate constant of the catalytic oxidation of acyclovir and the electron-transfer coefficient are reported. A sensitive, simple and time-saving amperometric procedure was developed for the analysis of acyclovir. The proposed amperometric method was also applied to determine acyclovir in tablets and topical cream.

  11. Fabrication and Investigation of Nickel-Alkaline Cells. Part 1. Fabrication of Nickel-Hydroxide Electrodes Using Electrochemical Impregnation Techniques

    DTIC Science & Technology

    1975-10-01

    electrodes show capacities as high as 9.5 ampere-hours per cubic inch after these cycles. The alcohol process has been scaled to pilot production, FORM 1473...expel residual nitrogen as ammonia. This procedure must be repeated several * Presently only nickel-cadmium cells are used in Air Force missions; Nickel...hydrates of nickel and cadmium nitrates followed by a heat treatment to decompose the imbibed nitrates to hydroxides(2,3). The final process in all Ni-Cd

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

    DOEpatents

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

    1994-01-01

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

  13. 3D Imaging of Nickel Oxidation States using Full Field X-ray Absorption Near Edge Structure Nanotomography

    SciTech Connect

    Nelson, George; Harris, William; Izzo, John; Grew, Kyle N.

    2012-01-20

    Reduction-oxidation (redox) cycling of the nickel electrocatalyst phase in the solid oxide fuel cell (SOFC) anode can lead to performance degradation and cell failure. A greater understanding of nickel redox mechanisms at the microstructural level is vital to future SOFC development. Transmission x-ray microscopy (TXM) provides several key techniques for exploring oxidation states within SOFC electrode microstructure. Specifically, x-ray nanotomography and x-ray absorption near edge structure (XANES) spectroscopy have been applied to study samples of varying nickel (Ni) and nickel oxide (NiO) compositions. The imaged samples are treated as mock SOFC anodes containing distinct regions of the materials in question. XANES spectra presented for the individual materials provide a basis for the further processing and analysis of mixed samples. Images of composite samples obtained are segmented, and the distinct nickel and nickel oxide phases are uniquely identified using full field XANES spectroscopy. Applications to SOFC analysis are discussed.

  14. Evaluation of the effects of oxygen evolution on the capacity and cycle life of nickel hydroxide electrode materials

    NASA Astrophysics Data System (ADS)

    Snook, Graeme A.; Duffy, Noel W.; Pandolfo, Anthony G.

    The effect of charge-discharge cycling on the capacity of surface-adhered nickel hydroxide (Ni(OH) 2) micro-particles is investigated in aqueous KOH by cyclic voltammetry, and compared with that for pasted nickel hydroxide electrodes. Cyclic voltammetry on adhered Ni(OH) 2 micro-particles enables rapid screening of four types of commercially available, battery-grade, nickel hydroxide samples and allows the separation of the oxidation process from the oxygen evolution reaction. With large pasted electrodes, due to their high uncompensated resistance (R u), these processes are poorly resolved. Pasted β-nickel hydroxide electrodes with a specific capacity of between 190 and 210 mAh g -1 are charged and discharged at constant currents greater than 15 C (18 mA cm -2). With no voltage limit in the charging profile, excess oxygen evolution occurs and capacity fading is observed within the first 50 cycles. Loss of capacity is attributed to the degradation of the electrode due to excess oxygen evolution at switching potentials greater than 0.55 V versus Hg/HgO (1 M KOH). X-ray diffraction (XRD) measurements confirm the formation of γ-NiOOH in these electrodes. Limiting the cell voltage to 1.5 V, and thereby minimizing oxygen evolution, results in no observed capacity loss within 100 cycles, and only β-Ni(OH) 2 can be detected by XRD phase analysis.

  15. Direct electrochemistry and electrocatalytic activity of catalase immobilized onto electrodeposited nano-scale islands of nickel oxide.

    PubMed

    Salimi, Abdollah; Sharifi, Ensiyeh; Noorbakhsh, Abdollah; Soltanian, Saied

    2007-02-01

    Cyclic voltammetry was used for simultaneous formation and immobilization of nickel oxide nano-scale islands and catalase on glassy carbon electrode. Electrodeposited nickel oxide may be a promising material for enzyme immobilization owing to its high biocompatibility and large surface. The catalase films assembled on nickel oxide exhibited a pair of well defined, stable and nearly reversible CV peaks at about -0.05 V vs. SCE at pH 7, characteristic of the heme Fe (III)/Fe (II) redox couple. The formal potential of catalase in nickel oxide film were linearly varied in the range 1-12 with slope of 58.426 mV/pH, indicating that the electron transfer is accompanied by single proton transportation. The electron transfer between catalase and electrode surface, (k(s)) of 3.7(+/-0.1) s(-1) was greatly facilitated in the microenvironment of nickel oxide film. The electrocatalytic reduction of hydrogen peroxide at glassy carbon electrode modified with nickel oxide nano-scale islands and catalase enzyme has been studied. The embedded catalase in NiO nanoparticles showed excellent electrocatalytic activity toward hydrogen peroxide reduction. Also the modified rotating disk electrode shows good analytical performance for amperometric determination of hydrogen peroxide. The resultant catalase/nickel oxide modified glassy carbon electrodes exhibited fast amperometric response (within 2 s) to hydrogen peroxide reduction (with a linear range from 1 microM to 1 mM), excellent stability, long term life and good reproducibility. The apparent Michaelis-Menten constant is calculated to be 0.96(+/-0.05)mM, which shows a large catalytic activity of catalase in the nickel oxide film toward hydrogen peroxide. The excellent electrochemical reversibility of redox couple, high stability, technical simplicity, lake of need for mediators and short preparations times are advantages of this electrode. Finally the activity of biosensor for nitrite reduction was also investigated.

  16. Electrochemistry of norepinephrine on carbon-coated nickel magnetic nanoparticles modified electrode and analytical applications.

    PubMed

    Bian, Chunli; Zeng, Qingxiang; Xiong, Huayu; Zhang, Xiuhua; Wang, Shengfu

    2010-08-01

    A carbon-coated nickel magnetic nanoparticles modified glassy carbon electrode (C-Ni/GCE) was fabricated. The carbon-coated nickel magnetic nanoparticles were characterized with transmission electron microscopy (TEM). The electrochemical behaviors of norepinephrine (NE) were investigated on the modified electrode by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The carbon-coated nickel magnetic nanoparticles showed excellent electrocatalytic activity for the electrochemical redox of NE. NE exhibited two couples of well-defined redox peaks on C-Ni/GCE over the potential range from -0.4 to 0.8V in phosphate buffer solution (PBS) (pH=7.0). The redox mechanism for NE was proposed. DPV response of NE on the C-Ni/GCE showed that the catalytic oxidative peak current was linear with the square root concentration of NE in the range of 2.0 x 10(-7) to 8.0 x 10(-5)M, with a detection limit of 6.0 x 10(-8)M. The C-Ni/GCE showed good sensitivity, selectivity and stability for the determination of NE.

  17. Progress in the development of lightweight nickel electrode for aerospace applications

    NASA Technical Reports Server (NTRS)

    Britton, Doris L.

    1992-01-01

    The NASA Lewis Research Center is currently developing nickel electrodes for nickel-hydrogen (Ni-H2) cells and batteries. These electrodes are lighter in weight and have higher specific energy than the heavy sintered state of the art nickel electrodes. In the present approach, lightweight materials or plaques are used as conductive supports for the nickel hydroxide active material. These plaques (fiber, felt, and nickel plated plastic) are fabricated into nickel electrodes by electrochemically impregnating them with active material. Initial performance tests include capacity measurements at five discharge levels, C/2, 1.0C, 1.37C, 2.0C, and 2.74C. The electrodes that pass the initial tests are life cycle tested at 40 and 80 percent depths of discharge (DOD). Different formulations of nickel fiber materials obtained from several manufacturers are currently being tested as possible candidates for nickel electrodes. Over 7,000 cycles of life cycle testing have been accumulated at 40 percent DOD, using the lightweight fiber electrode in a boiler plate Ni-H2 cell with stable voltage.

  18. Gas-phase reactions of nickel and nickel oxide clusters with nitrogen oxides. 3. Reactions of cations with nitric oxide

    SciTech Connect

    Vann, W.D.; Bell, R.C.; Castleman, A.W. Jr.

    1999-12-16

    A fast flow reactor-quadrupole mass spectrometer system coupled with a laser vaporization source is used to study the gas-phase reactions of nickel and nickel oxide cluster cations with nitric oxide. Pseudo-first-order bimolecular rate constants are reported for the reactions of NO with nickel and nickel oxide cluster cations and O{sub 2} reactions with nickel cluster cations. The product distributions indicate that several different reaction mechanisms occur between NO and NI{sub x}{sup +} and Ni{sub x}O{sub y}{sup +}. Competing processes such as oxidation, NO addition, and replacement of oxygen with nitric oxide are observed to occur. Also, the presence of magic peaks in the distributions indicates unusually stable product cluster species.

  19. Photo-enhanced oxidation of nickel

    NASA Astrophysics Data System (ADS)

    Mesarwi, A.; Ignatiev, A.; Liu, J. S.

    1988-02-01

    The oxidation in air of polycrystalline nickel samples at bulk temperatures of 400°C and 500°C under both infrared oven heating and high flux visible/near u.v. irradiation (⩾ 1 MW/m 2) is examined. The oxide thickness is found to be over 400% greater under photo-irradiation at 3.5 MW/m 2 and 400°C bulk temperature than under infrared irradiation at an equivalent temperature. Also, the oxide thickness is found to increase linearly with increasing flux. This photo-enhanced oxidation is believed to be mainly due to electronic excitation of the surface adsorbed molecular oxygen species with subsequent enhanced dissociation. This leads to increased oxidation kinetics and ultimately to the observed increase in oxide thickness.

  20. Electrospinning of nickel oxide nanofibers: Process parameters and morphology control

    SciTech Connect

    Khalil, Abdullah Hashaikeh, Raed

    2014-09-15

    In the present work, nickel oxide nanofibers with varying morphology (diameter and roughness) were fabricated via electrospinning technique using a precursor composed of nickel acetate and polyvinyl alcohol. It was found that the diameter and surface roughness of individual nickel oxide nanofibers are strongly dependent upon nickel acetate concentration in the precursor. With increasing nickel acetate concentration, the diameter of nanofibers increased and the roughness decreased. An optimum concentration of nickel acetate in the precursor resulted in the formation of smooth and continuous nickel oxide nanofibers whose diameter can be further controlled via electrospinning voltage. Beyond an optimum concentration of nickel acetate, the resulting nanofibers were found to be ‘flattened’ and ‘wavy’ with occasional cracking across their length. Transmission electron microscopy analysis revealed that the obtained nanofibers are polycrystalline in nature. These nickel oxide nanofibers with varying morphology have potential applications in various engineering domains. - Highlights: • Nickel oxide nanofibers were synthesized via electrospinning. • Fiber diameter and roughness depend on nickel acetate concentration used. • With increasing nickel acetate concentration the roughness of nanofibers decreased. • XRD and TEM revealed a polycrystalline structure of the nanofibers.

  1. Fabrication of nickel microbump on aluminum using electroless nickel plating

    SciTech Connect

    Watanabe, H.; Honma, H.

    1997-02-01

    Fabrication of nickel microbumps on an aluminum electrode using a nickel displacement and a direct nickel plating process was investigated. Electroless nickel plating reaction with hypophosphite as a reducing agent was not initiated on the aluminum substrate, because aluminum does not have catalytic action on the oxidation of hypophosphite. Accordingly, nickel was initially deposited on the aluminum using nickel displacement plating for the initiation of the electroless plating. Nickel bumps on the aluminum electrode were fabricated by treatment of the nickel displacement plating followed by electroless nickel plating. Nickel microbumps also can be formed on the aluminum electrode without the displacement plating process. Activation of the aluminum surface is an indispensable process to initiate electroless nickel plating. Uniform bumps 20 {micro}m wide and 15 {micro}m high with good configuration were obtained by direct nickel plating after being activated with dimethyl amine borane.

  2. Control of edge effects of oxidant electrode

    DOEpatents

    Carr, Peter; Chi, Chen H.

    1981-09-08

    Described is an electrode assembly comprising; a. a porous electrode having a first and second exterior face with a cavity formed in the interior between said exterior faces thereby having first and second interior faces positioned opposite the first and second exterior faces; b. a counter electrode positioned facing each of the first and second exterior faces of the porous electrode; c. means for passing an oxidant through said porous electrode; and d. screening means for blocking the interior face of the porous electrode a greater amount than the blocking of the respective exterior face of the porous electrode, thereby maintaining a differential of oxidant electrode surface between the interior face and the exterior face. The electrode assembly is useful in a metal, halogen, halogen hydrate electrical energy storage device.

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

    NASA Technical Reports Server (NTRS)

    Ford, F.; Paulkovitch, J.

    1968-01-01

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

  4. The structures of the sintered plaque in the nickel hydroxide electrode

    NASA Technical Reports Server (NTRS)

    Vyas, B.

    1981-01-01

    The various failure mechanisms were identified for the nickel electrode. The nickel sinter is involved in all these failure modes. The first one, chemical attack by carbonate, nitrate or other electrolyte components, involves corrosion of the nickel sinters. The second is the physical mode, which involves swelling of the electrode and physical shifting of the sinter in the electrodes. The third is the mechanical failure mode, and is due to fatigue or to the oxygen pressure that causes deformation or fracture of the sinter.

  5. The structures of the sintered plaque in the nickel hydroxide electrode

    NASA Technical Reports Server (NTRS)

    Vyas, B.

    1981-01-01

    The various failure mechanisms were identified for the nickel electrode. The nickel sinter is involved in all these failure modes. The first one, chemical attack by carbonate, nitrate or other electrolyte components, involves corrosion of the nickel sinters. The second is the physical mode, which involves swelling of the electrode and physical shifting of the sinter in the electrodes. The third is the mechanical failure mode, and is due to fatigue or to the oxygen pressure that causes deformation or fracture of the sinter.

  6. Nanoscale Ni-B electrocatalyst prepared from nickel ethylenediamine complex for direct ethanol electrocatalytic oxidation.

    PubMed

    Hou, Yongjiang; Guo, Jie; Li, Bo; Wang, Yaquan; Cai, Yuxi; Zhou, Zhenhuan

    2014-09-01

    Ni-B/Cu electrode prepared by the electroless deposition technique of chemical reduction of nickel ethylenediamine complex with BH4- was characterized by SEM, XRD and XPS techniques, respectively, and evaluated using ethanol electrocatalytic oxidation by the method of cyclic voltammetry. The as-prepared Ni-B/Cu electrode exhibited much higher electrocatalytic activity than the Ni-B/Cu electrode obtained via direct reduction of nickel metallic ions. The effects of the nickel ethylenediamine complex can be attributed to both the structural effect and electronic effect. The nickel ethylenediamine complex can not only make an electroless deposition stable and highly dispersed, but also facilitate the formation of more nanoscale microcrystalline Ni on the electrode surface, which increased the electrochemical oxidation activity. Moreover, ethylenediamine influenced the electronic states of Ni and B on the electrode surface, more electrons transfer from the B to Ni that the Ni active sites became more highly unsaturated, which could promote the form of adsorbed active ethanol.

  7. An electrochemical acetylcholine sensor based on lichen-like nickel oxide nanostructure.

    PubMed

    Sattarahmady, N; Heli, H; Vais, R Dehdari

    2013-10-15

    Lichen-like nickel oxide nanostructure was synthesized by a simple method and characterized. The nanostructure was then applied to modify a carbon paste electrode and for the fabrication of a sensor, and the electrocatalytic oxidation of acetylcholine (ACh) on the modified electrode was investigated. The electrocatalytic efficiency of the nickel oxide nanostructure was compared with nickel micro- and nanoparticles, and the lichen-like nickel oxide nanostructure showed the highest efficiency. The mechanism and kinetics of the electrooxidation process were investigated by cyclic voltammetry, steady-state polarization curve and chronoamperometry. The catalytic rate constant and the charge transfer coefficient of ACh electrooxidation by the active nickel species, and the diffusion coefficient of ACh were reported. A sensitive and time-saving hydrodynamic amperometry method was developed for the determination of ACh. ACh was determined with a sensitivity of 392.4 mA M⁻¹ cm⁻² and a limit of detection of 26.7 μM. The sensor had the advantages of simple fabrication method without using any enzyme or reagent and immobilization step, high electrocatalytic activity, very high sensitivity, long-term stability, and antifouling surface property toward ACh and its oxidation product.

  8. Pulse electrodeposited nickel-indium tin oxide nanocomposite as an electrocatalyst for non-enzymatic glucose sensing.

    PubMed

    Sivasakthi, P; Ramesh Bapu, G N K; Chandrasekaran, Maruthai

    2016-01-01

    Nickel and nickel-ITO nanocomposite on mild steel substrate were prepared by pulse electrodeposition method from nickel sulphamate electrolyte and were examined as electrocatalysts for non-enzymatic glucose sensing. The surface morphology, chemical composition, preferred orientation and oxidation states of the nickel metal ion in the deposits were characterized by SEM, EDAX, XRD and XPS. Electrochemical sensing of glucose was studied by cyclic voltammetry and amperometry. The modified Ni-ITO nanocomposite electrode showed higher electrocatalytic activity for the oxidation of glucose in alkaline medium and exhibited a linear range from 0.02 to 3.00 mM with a limit of detection 3.74 μM at a signal-to-noise ratio of 3. The higher selectivity, longer stability and better reproducibility of this electrode compared to nickel in the sensing of glucose are pointers for exploitation in practical clinical applications.

  9. Nanoscale nickel oxide/nickel heterostructures for active hydrogen evolution electrocatalysis

    NASA Astrophysics Data System (ADS)

    Gong, Ming; Zhou, Wu; Tsai, Mon-Che; Zhou, Jigang; Guan, Mingyun; Lin, Meng-Chang; Zhang, Bo; Hu, Yongfeng; Wang, Di-Yan; Yang, Jiang; Pennycook, Stephen J.; Hwang, Bing-Joe; Dai, Hongjie

    2014-08-01

    Active, stable and cost-effective electrocatalysts are a key to water splitting for hydrogen production through electrolysis or photoelectrochemistry. Here we report nanoscale nickel oxide/nickel heterostructures formed on carbon nanotube sidewalls as highly effective electrocatalysts for hydrogen evolution reaction with activity similar to platinum. Partially reduced nickel interfaced with nickel oxide results from thermal decomposition of nickel hydroxide precursors bonded to carbon nanotube sidewalls. The metal ion-carbon nanotube interactions impede complete reduction and Ostwald ripening of nickel species into the less hydrogen evolution reaction active pure nickel phase. A water electrolyzer that achieves ~20 mA cm-2 at a voltage of 1.5 V, and which may be operated by a single-cell alkaline battery, is fabricated using cheap, non-precious metal-based electrocatalysts.

  10. Three-electrode metal oxide reduction cell

    DOEpatents

    Dees, Dennis W.; Ackerman, John P.

    2008-08-12

    A method of electrochemically reducing a metal oxide to the metal in an electrochemical cell is disclosed along with the cell. Each of the anode and cathode operate at their respective maximum reaction rates. An electrolyte and an anode at which oxygen can be evolved, and a cathode including a metal oxide to be reduced are included as is a third electrode with independent power supplies connecting the anode and the third electrode and the cathode and the third electrode.

  11. Three-Electrode Metal Oxide Reduction Cell

    DOEpatents

    Dees, Dennis W.; Ackerman, John P.

    2005-06-28

    A method of electrochemically reducing a metal oxide to the metal in an electrochemical cell is disclosed along with the cell. Each of the anode and cathode operate at their respective maximum reaction rates. An electrolyte and an anode at which oxygen can be evolved, and a cathode including a metal oxide to be reduced are included as is a third electrode with independent power supplies connecting the anode and the third electrode and the cathode and the third electrode.

  12. Nickel vacancy behavior in the electrical conductance of nonstoichiometric nickel oxide film

    SciTech Connect

    Kim, Dong Soo; Lee, Hee Chul

    2012-08-01

    Nickel vacancy behavior in electrical conductance is systematically investigated using various analysis methods on nickel oxide films deposited at different oxygen partial pressures. The results of Rutherford backscattering, x-ray diffraction, and Auger electron spectroscopy analyses demonstrate that the sputtered nickel oxide films are nickel-deficient. Through the deconvolution of Ni2p and O1s spectra in the x-ray photoelectron spectroscopy data, the number of Ni{sup 3+} ions is found to increase with the O{sub 2} ratio during the deposition. According to the vacancy model, nickel vacancies created from the non-stoichiometry are concluded to produce Ni{sup 3+} ions which lead to an increment of the conductivity of the nickel oxide films due to the increase of the hole concentration.

  13. Reliability of multilayer ceramic capacitors with nickel electrodes

    NASA Astrophysics Data System (ADS)

    Yamamatsu, J.; Kawano, N.; Arashi, T.; Sato, A.; Nakano, Y.; Nomura, T.

    The reliability of multilayer ceramic capacitors (MLCCs) with Ni internal electrodes has been studied trom the viewpoint of partial oxygen pressure ( PO2) during firing. It is shown that the load-life time of the insulation resistance (1R) was prolonged by firing under low Po 2 annealing after firing, and the addition of dopants. It is also shown that the generation of oxygen vacancies led to the degradation of IR. Annealing treatment for the oxidation of the dielectric body accelerates the dielectric aging of MLCCs. It is found that the appropriate control of the PO2 during firing can improve the reliability of MLCCs with Ni electrodes to a level as high as that of MLCCs with precious metal electrodes. Thus, we have developed an MLCC with Ni electrodes that features high reliability and a large capacitance of 10 μF for the Y5V characteristic and 4.7 μF for the X7R characteristic, both in the case of the C3216 (3.2 mm × 1.6 mm × 1.4 mm) form.

  14. Effect of impregnation method on cycle life of the nickel electrode

    NASA Technical Reports Server (NTRS)

    Smithrick, J. J.

    1986-01-01

    The nickel electrode has been identified as the life limiting component for individual pressure vessel (IPV) nickel-hydrogen cells when cycled under a low earth orbit (LEO) cycle regime at deep depths of discharge. As a part of an overall program to develop a long life nickel electrode for nickel-hydrogen cells, the effect of two different methods of electrochemical impregnation on the cycle life of the nickel electrode was investigated. One method was the Pickett (aqueous/ethanolic) process. The other was the modified Bell (aqueous) process. The plaques for both impregnation methods were made by sintering dry carbonyl nickel powder in a reducing atmosphere. The plaques contain a nickel screen substrate. Electrodes made from both processes were cycle tested in Air Force design IPV nickel-hydrogen cells. The only factor different for this test was the method of plaque impregnation; all other factors were the same. The cells were cycled to failure under a 90 min LEO cycle regime at a deep depth of discharge (80 percent DOD). Failure for this test was defined to occur when the cell voltage degraded to 1.0 V prior to the completion of the 35 min discharge.

  15. Method of making porous conductive supports for electrodes. [by electroforming and stacking nickel foils

    NASA Technical Reports Server (NTRS)

    Schaer, G. R. (Inventor)

    1973-01-01

    Porous conductive supports for electrochemical cell electrodes are made by electroforming thin corrugated nickel foil, and by stacking pieces of the corrugated foil alternatively with pieces of thin flat nickel foil. Corrugations in successive corrugated pieces are oriented at different angles. Adjacent pieces of foil are bonded by heating in a hydrogen atmosphere and then cutting the stack in planes perpendicular to the foils.

  16. Structural comparison of nickel electrodes and precursor phases

    NASA Technical Reports Server (NTRS)

    Cornilsen, Bahne C.; Shan, Xiaoyin; Loyselle, Patricia

    1989-01-01

    A summary of previous Raman spectroscopic results and a discussion of important structural differences in the various phases of active mass and active mass precurors are presented. Raman spectra provide unique signatures for these phases, and allow one to distinguish each phase, even when the compound is amorphous to X-rays (i.e., does not scatter X-rays because of a lack of order and/or small particle size). The structural changes incurred during formation, charge and discharge, cobalt addition, and aging will be discussed and related to electrode properties. Important structural differences include NiO2 layer stacking, nonstoichiometry (especially cation-deficit nonstoichiometry), disorder, dopant content, and water content. The results indicate that optimal nickel active mass is non-close packed and nonstoichiometric. The formation process transforms precursor phases into this structure. Therefore, the precursor disorder, or lack thereof, influences this final active mass structure and the rate of formation. Aging processes induce structural change which is believed to be detrimental. The role of cobalt addition can be appreciated in terms of structures favored or stabilized by the dopant. In recent work, the in situ Raman technique to characterize the critical structural parameters was developed. An in situ method relates structure, electrochemistry, and preparation. In situ Raman spectra of cells during charge and discharge, either during cyclic voltammetry or under constant current conditions were collected. With the structure-preparation knowledge and the in situ Raman tool, it will be possible to define the structure-property-preparation relations in more detail. This instrumentation has application to a variety of electrode systems.

  17. Silver manganese oxide electrodes for lithium batteries

    DOEpatents

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

    2006-05-09

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

  18. Green synthesized nickel nanoparticles modified electrode in ionic liquid medium and its application towards determination of biomolecules.

    PubMed

    Babu, Rajendran Suresh; Prabhu, Pandurangan; Narayanan, Sangilimuthu Sriman

    2013-06-15

    An air and moisture stable ionic liquid 1-ethyl-3-methylimidazolium ethyl sulfate (EMIMES) was used as an electrolyte for electropolymerization of L-cysteine followed by electrodeposition of nickel nanoparticles (NiNP) on paraffin wax impregnated graphite electrode (PIGE). The electrodeposited NiNP modified electrode showed good redox activity and stability in 0.1M KOH solution. The modified electrode has been characterized using Fourier transform infrared spectroscopy (FTIR), Raman spectroscopy, X-ray photoelectron spectroscopy (XPS), field emission scanning electron microscopy (FESEM), energy dispersive X-ray spectroscopy (EDS), electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV). The modified electrode was examined for electrocatalytic oxidation of some compounds of biological and clinical importance such as vitamin B6, L-tyrosine, L-tryptophan, vanillin, glucose and hydrogen peroxide by cyclic voltammetry to demonstrate the electrocatalytic activity of the electrodeposited NiNPs.

  19. 40 CFR 721.10201 - Cobalt lithium manganese nickel oxide.

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Cobalt lithium manganese nickel oxide... Specific Chemical Substances § 721.10201 Cobalt lithium manganese nickel oxide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as cobalt lithium manganese...

  20. 40 CFR 721.10201 - Cobalt lithium manganese nickel oxide.

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Cobalt lithium manganese nickel oxide... Specific Chemical Substances § 721.10201 Cobalt lithium manganese nickel oxide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as cobalt lithium manganese...

  1. 40 CFR 721.10201 - Cobalt lithium manganese nickel oxide.

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Cobalt lithium manganese nickel oxide... Specific Chemical Substances § 721.10201 Cobalt lithium manganese nickel oxide. (a) Chemical substance and significant new uses subject to reporting. (1) The chemical substance identified as cobalt lithium manganese...

  2. X7R Multilayer Ceramic Capacitors with Nickel Electrodes

    NASA Astrophysics Data System (ADS)

    Saito, Hiroshi; Chazono, Hirokazu; Kishi, Hiroshi; Yamaoka, Nobutatsu

    1991-09-01

    Electrical properties and microstructures of a holmium-doped (Ba1.01Mg0.01)O1.02(Ti0.98Zr0.02)O2 system were studied. Additions of Ho2O3 had little effect in preventing the dielectrics from reducing at high temperature, but the resistivity at low temperature increased with increasing amount of Ho2O3 when treated in oxidizing atmosphere at the cooling stage. From transmission electron micrograph (TEM) observation, it was noted that the microstructure exhibited a grain core-grain shell structure. Newly developed X7R multilayer ceramic capacitors with Ni electrodes revealed highly reliable electrical properties.

  3. A highly efficient microfluidic nano biochip based on nanostructured nickel oxide

    NASA Astrophysics Data System (ADS)

    Ali, Md. Azahar; Solanki, Pratima R.; Patel, Manoj K.; Dhayani, Hemant; Agrawal, Ved Varun; John, Renu; Malhotra, Bansi D.

    2013-03-01

    We present results of the studies relating to fabrication of a microfluidic biosensor chip based on nickel oxide nanorods (NRs-NiO) that is capable of directly measuring the concentration of total cholesterol in human blood through electrochemical detection. Using this chip we demonstrate, with high reliability and in a time efficient manner, the detection of cholesterol present in buffer solutions at clinically relevant concentrations. The microfluidic channel has been fabricated onto a nickel oxide nanorod-based electrode co-immobilized with cholesterol esterase (ChEt) and cholesterol oxidase (ChOx) that serves as the working electrode. Bare indium tin oxide served as the counter electrode. A Ag/AgCl wire introduced to the outlet of the microchannel acts as a reference electrode. The fabricated NiO nanorod-based electrode has been characterized using X-ray diffraction, Raman spectroscopy, HR-TEM, FT-IR, UV-visible spectroscopy and electrochemical techniques. The presented NRs-NiO based microfluidic sensor exhibits linearity in the range of 1.5-10.3 mM, a high sensitivity of 0.12 mA mM-1 cm-2 and a low value of 0.16 mM of the Michaelis-Menten constant (Km).We present results of the studies relating to fabrication of a microfluidic biosensor chip based on nickel oxide nanorods (NRs-NiO) that is capable of directly measuring the concentration of total cholesterol in human blood through electrochemical detection. Using this chip we demonstrate, with high reliability and in a time efficient manner, the detection of cholesterol present in buffer solutions at clinically relevant concentrations. The microfluidic channel has been fabricated onto a nickel oxide nanorod-based electrode co-immobilized with cholesterol esterase (ChEt) and cholesterol oxidase (ChOx) that serves as the working electrode. Bare indium tin oxide served as the counter electrode. A Ag/AgCl wire introduced to the outlet of the microchannel acts as a reference electrode. The fabricated NiO nanorod

  4. Cobalt oxide nanosheets wrapped onto nickel foam for non-enzymatic detection of glucose

    NASA Astrophysics Data System (ADS)

    Meng, Shangjun; Wu, Meiyan; Wang, Qian; Dai, Ziyang; Si, Weili; Huang, Wei; Dong, Xiaochen

    2016-08-01

    Ultra-sensitive and highly selective detection of glucose is essential for the clinical diagnosis of diabetes. In this paper, an ultra-sensitive glucose sensor was successfully fabricated based on cobalt oxide (Co3O4) nanosheets directly grown on nickel foam through a simple hydrothermal method. Characterizations indicated that the Co3O4 nanosheets are completely and uniformly wrapped onto the surface of nickel foam to form a three-dimensional heterostructure. The resulting self-standing electrochemical electrode presents a high performance for the non-enzymatic detection of glucose, including short response time (<10 s), ultra-sensitivity (12.97 mA mM-1 cm-2), excellent selectivity and low detection limit (0.058 μM, S/N = 3). These results indicate that Co3O4 nanosheets wrapped onto nickel foam are a low-cost, practical, and high performance electrochemical electrode for bio sensing.

  5. Nickel-silver alloy electrocatalysts for hydrogen evolution and oxidation in an alkaline electrolyte.

    PubMed

    Tang, Maureen H; Hahn, Christopher; Klobuchar, Aidan J; Ng, Jia Wei Desmond; Wellendorff, Jess; Bligaard, Thomas; Jaramillo, Thomas F

    2014-09-28

    The development of improved catalysts for the hydrogen evolution reaction (HER) and hydrogen oxidation reaction (HOR) in basic electrolytes remains a major technical obstacle to improved fuel cells, water electrolyzers, and other devices for electrochemical energy storage and conversion. Based on the free energy of adsorbed hydrogen intermediates, theory predicts that alloys of nickel and silver are active for these reactions. In this work, we synthesize binary nickel-silver bulk alloys across a range of compositions and show that nickel-silver alloys are indeed more active than pure nickel for hydrogen evolution and, possibly, hydrogen oxidation. To overcome the mutual insolubility of silver and nickel, we employ electron-beam physical vapor codeposition, a low-temperature synthetic route to metastable alloys. This method also produces flat and uniform films that facilitate the measurement of intrinsic catalytic activity with minimal variations in the surface area, ohmic contact, and pore transport. Rotating-disk-electrode measurements demonstrate that the hydrogen evolution activity per geometric area of the most active catalyst in this study, Ni0.75Ag0.25, is approximately twice that of pure nickel and has comparable stability and hydrogen oxidation activity. Our experimental results are supported by density functional theory calculations, which show that bulk alloying of Ni and Ag creates a variety of adsorption sites, some of which have near-optimal hydrogen binding energy.

  6. Novel methods of stabilization of Raney-Nickel catalyst for fuel-cell electrodes

    NASA Astrophysics Data System (ADS)

    Al-Saleh, M. A.; Sleem-Ur-Rahman; Kareemuddin, S. M. M. J.; Al-Zakri, A. S.

    Two new methods of stabilizing Raney-Nickel (Raney-Ni) catalyst for making fuel-cell anodes were studied. In the first method, the catalyst was oxidized with aqueous H 2O 2 solution, while in the second, oxygen/air (O 2/air) was used in a slurry reactor. Effects of different concentrations of H 2O 2 (5-25 wt.%) and different pressures (10-20 psig) of gas were investigated. The stabilized catalyst was characterized using BET surface area, scanning electron microscopy (SEM) and X-ray diffraction (XRD). The catalyst was used in fuel-cell anodes and the electrochemical performance was determined in an alkaline half-cell. The results were compared with electrodes prepared using conventionally stabilized catalysts. The hydrogen peroxide-treated catalyst has higher BET surface area and produces electrodes with lower polarization. In addition to this, H 2O 2 treatment is convenient, fast and needs simple equipment which involves no instrumentation. Use of oxygen in a slurry reactor to stabilize the catalyst is also convenient but electrode performance is relatively poor.

  7. Effects of Electrodes on the Switching Behavior of Strontium Titanate Nickelate Resistive Random Access Memory

    PubMed Central

    Lee, Ke-Jing; Wang, Li-Wen; Chiang, Te-Kung; Wang, Yeong-Her

    2015-01-01

    Strontium titanate nickelate (STN) thin films on indium tin oxide (ITO)/glass substrate were synthesized using the sol-gel method for resistive random access memory (RRAM) applications. Aluminum (Al), titanium (Ti), tungsten (W), gold (Au) and platinum (Pt) were used as top electrodes in the STN-based RRAM to probe the switching behavior. The bipolar resistive switching behavior of the set and reset voltages is in opposite bias in the Al/STN/ITO and Pt/STN/ITO RRAMs, which can be partly ascribed to the different work functions of top electrodes in the ITO. Analyses of the fitting results and temperature-dependent performances showed that the Al/STN/ITO switching was mainly attributed to the absorption/release of oxygen-based functional groups, whereas the Pt/STN/ITO switching can be associated with the diffusion of metal electrode ions. The Al/STN/ITO RRAM demonstrated a high resistance ratio of >106 between the high-resistance state (HRS) and the low-resistance state (LRS), as well as a retention ability of >105 s. Furthermore, the Pt/STN/ITO RRAM displayed a HRS/LRS resistance ratio of >103 and a retention ability of >105 s. PMID:28793630

  8. Heat- And Oxidation-Resistant Electrodes

    NASA Technical Reports Server (NTRS)

    Schroeder, James E.

    1990-01-01

    Alloys coated with electrically conductive ceramics used to make strong, oxidation-resistant electrodes for electrochemical cells operating at temperatures of 1,000 to 1,300 degrees C. Fe3Al or Ni3Al coated with strontium-doped lanthanum manganite more resistant to chemical attack than all-metal electrode, less brittle than all-ceramic electrode, and less costly than either alternative.

  9. Gas-phase reactions of nickel and nickel-rich oxide cluster anions with nitric oxide. 2: The addition of nitric oxide, oxidation of nickel clusters, and the formation of nitrogen oxide anions

    SciTech Connect

    Vann, W.D.; Wagner, R.L.; Castleman, A.W. Jr.

    1998-11-05

    A fast flow reactor-quadrupole mass spectrometer coupled with a laser vaporization source is used to study the gas-phase reactions of nickel and nickel oxide cluster anions (Ni{sub x}O{sub y}{sup {minus}}, where x = 1--12 and y = 0, 1, or 2) with nitric oxide. The results indicate that three processes are occurring in the presence of the nickel cluster anions. First, nickel and nickel oxide clusters are oxidized by the reaction with nitric oxide. Second, addition products with these oxides are also formed. Third, nitrogen dioxide and nitrogen trioxide are formed on nickel oxide clusters and subsequently released as anions. Rate constants are reported for the initial reaction occurring between the nickel cluster anions and the nitric oxide, and the reaction rates are compared with reaction rates of the same nickel anion clusters with molecular oxygen. Finally, a comparison of the reaction rates for nickel oxides formed both in the flow tube and in the laser vaporization source are reported. These reactions (previously reported on Part 1) to help to provide a better understanding of the formation of free nitrogen oxide anions observed in the current experiments.

  10. Surface protected lithium-metal-oxide electrodes

    DOEpatents

    Thackeray, Michael M.; Kang, Sun-Ho

    2016-04-05

    A lithium-metal-oxide positive electrode having a layered or spinel structure for a non-aqueous lithium electrochemical cell and battery is disclosed comprising electrode particles that are protected at the surface from undesirable effects, such as electrolyte oxidation, oxygen loss or dissolution by one or more lithium-metal-polyanionic compounds, such as a lithium-metal-phosphate or a lithium-metal-silicate material that can act as a solid electrolyte at or above the operating potential of the lithium-metal-oxide electrode. The surface protection significantly enhances the surface stability, rate capability and cycling stability of the lithium-metal-oxide electrodes, particularly when charged to high potentials.

  11. A flower-like nickel oxide nanostructure: synthesis and application for choline sensing.

    PubMed

    Sattarahmady, N; Heli, H; Dehdari Vais, R

    2014-02-01

    Flower-like nickel oxide nanostructure was synthesized by a simple desolvation method. The nanostructure was then employed as the modifier of a carbon paste electrode to fabricate a choline sensor. The mechanism and kinetics of the electrocatalytic oxidation of choline on the modified electrode surface were studied by cyclic voltammetry, steady-state polarization curve, and chronoamperometry. The catalytic rate constant and the charge transfer coefficient of the choline electrooxidation process by an active nickel species, and the diffusion coefficient of choline were reported. An amperometric method was developed for determination of choline with a sensitivity of 60.5 mA mol(-1)Lcm(-2) and a limit of detection of 25.4 μmol L(-1). The sensor had the advantages of high electrocatalytic activity and sensitivity, and long-term stability toward choline, with a simple fabrication method without complications of immobilization steps and using any enzyme or reagent.

  12. Effect of the bimetal ratio on the growth of nickel cobalt sulfide on the Ni foam for the battery-like electrode.

    PubMed

    Yu, Cheng-Fong; Lin, Lu-Yin

    2016-11-15

    The nickel cobalt sulfide is one of the most attractive electroactive materials for battery-like electrodes with multiple oxidation states for Faradaic reactions. Novel structures of the nickel cobalt sulfide with large surface areas and high conductivities have been proposed to improve the performance of the battery-like electrodes. The hydrothermal reaction is the most common used method for synthesizing nickel cobalt sulfide nanostructures due to the simple and cost-effective features, but the precursor concentration on the morphology and the resulting electrochemical performance is barely discussed. In this study, various Ni to Co ratios are used in the hydrothermal reaction to make nickel cobalt sulfides on the nickel foam, and the Ni to Co ratio is found to play great roles on the morphology and the electrocapacitive performance for the pertinent battery-like electrodes. The sheet-like structures are successfully obtained with large surface area for charge accumulation, and the optimized sample presents the largest nanosheets among all with several wrinkles on the surface. A high specific capacity of 258.2mAh/g measured at the current density of 5A/g and a high-rate charge/discharge capacity are also attended for the optimized battery-like electrodes. The excellent cycling stability of 94.5% retention after 2000 cycles repeated charge/discharge process is also obtained for this system.

  13. A nickel-borate nanoarray: a highly active 3D oxygen-evolving catalyst electrode operating in near-neutral water.

    PubMed

    Ji, Xuqiang; Cui, Liang; Liu, Danni; Hao, Shuai; Liu, Jingquan; Qu, Fengli; Ma, Yongjun; Du, Gu; Asiri, Abdullah M; Sun, Xuping

    2017-02-28

    The exploration of high-performance and cost-effective water oxidation catalysts operating under mild conditions is still urgent and challenging. In this communication, a nickel-borate nanoarray supported on carbon cloth (Ni-Bi/CC) has been fabricated through oxidative polarization of a nickel oxide nanoarray on CC (NiO/CC) in a borate electrolyte (pH 9.2). As a 3D electrode, this Ni-Bi/CC exhibits superior catalytic activity for water oxidation in 0.1 M potassium borate (K-Bi) solution, yielding a geometrical catalytic current density of 10 mA cm(-2) at an overpotential of 470 mV. Notably, this electrode also demonstrates outstanding long-term electrochemical durability for 25 h with 100% Faradaic efficiency.

  14. A Comparative Study of Microstructures and Properties of Two Types of Nickel-Base Alloy Covered Electrodes

    NASA Astrophysics Data System (ADS)

    Wang, Huang; He, Guo

    2017-01-01

    Two types of nickel-base alloy covered electrodes, ENiCrMo-6 and ENiCrFe-9, were investigated and compared among their deposited metal compositions, microstructures, strengths, and cryogenic impact values. They all exhibited dendritic microstructures which were composed of dendritic fcc nickel-base solid solution, interdendritic phases, and grain boundary carbides. The molybdenum in the deposited metals tended to migrate and aggregate toward the edges of the dendrite arms during solidification. The niobium preferred to form oxide and/or carbide and aggregate in the interdendritic regions. The grain boundaries were filled with the continuous carbides and oxides. The differences in the tensile mechanical properties of the deposited metals of the two types of electrodes were relatively minor. The impact values of ENiCrMo-6 at -196 °C were above 80 J; while that of ENiCrFe-9 were in the range of 54-66 J. The relatively high level of carbon and sulfur and more grain boundary precipitates should be responsible for the lower cryogenic impact value of the ENiCrFe-9 covered electrode.

  15. A Comparative Study of Microstructures and Properties of Two Types of Nickel-Base Alloy Covered Electrodes

    NASA Astrophysics Data System (ADS)

    Wang, Huang; He, Guo

    2016-11-01

    Two types of nickel-base alloy covered electrodes, ENiCrMo-6 and ENiCrFe-9, were investigated and compared among their deposited metal compositions, microstructures, strengths, and cryogenic impact values. They all exhibited dendritic microstructures which were composed of dendritic fcc nickel-base solid solution, interdendritic phases, and grain boundary carbides. The molybdenum in the deposited metals tended to migrate and aggregate toward the edges of the dendrite arms during solidification. The niobium preferred to form oxide and/or carbide and aggregate in the interdendritic regions. The grain boundaries were filled with the continuous carbides and oxides. The differences in the tensile mechanical properties of the deposited metals of the two types of electrodes were relatively minor. The impact values of ENiCrMo-6 at -196 °C were above 80 J; while that of ENiCrFe-9 were in the range of 54-66 J. The relatively high level of carbon and sulfur and more grain boundary precipitates should be responsible for the lower cryogenic impact value of the ENiCrFe-9 covered electrode.

  16. Is Steam an Oxidant or a Reductant for Nickel/Doped‐Ceria Cermets?

    PubMed Central

    Papaefthimiou, Vasiliki; Niakolas, Dimitris K.; Paloukis, Fotios; Dintzer, Thierry

    2016-01-01

    Abstract Nickel/doped‐ceria composites are promising electrocatalysts for solid‐oxide fuel and electrolysis cells. Very often steam is present in the feedstock of the cells, frequently mixed with other gases, such as hydrogen or CO2. An increase in the steam concentration in the feed mixture is considered accountable for the electrode oxidation and the deactivation of the device. However, direct experimental evidence of the steam interaction with nickel/doped‐ceria composites, with adequate surface specificity, are lacking. Herein we explore in situ the surface state of nickel/gadolinium‐doped ceria (NiGDC) under O2, H2, and H2O environments by using near‐ambient‐pressure X‐ray photoelectron and absorption spectroscopies. Changes in the surface oxidation state and composition of NiGDC in response to the ambient gas are observed. It is revealed that, in the mbar pressure regime and at intermediate temperature conditions (500–700 °C), steam acts as an oxidant for nickel but has a dual oxidant/reductant function for doped ceria. PMID:27792266

  17. Is Steam an Oxidant or a Reductant for Nickel/Doped-Ceria Cermets?

    PubMed

    Papaefthimiou, Vasiliki; Niakolas, Dimitris K; Paloukis, Fotios; Dintzer, Thierry; Zafeiratos, Spyridon

    2017-01-04

    Nickel/doped-ceria composites are promising electrocatalysts for solid-oxide fuel and electrolysis cells. Very often steam is present in the feedstock of the cells, frequently mixed with other gases, such as hydrogen or CO2 . An increase in the steam concentration in the feed mixture is considered accountable for the electrode oxidation and the deactivation of the device. However, direct experimental evidence of the steam interaction with nickel/doped-ceria composites, with adequate surface specificity, are lacking. Herein we explore in situ the surface state of nickel/gadolinium-doped ceria (NiGDC) under O2 , H2 , and H2 O environments by using near-ambient-pressure X-ray photoelectron and absorption spectroscopies. Changes in the surface oxidation state and composition of NiGDC in response to the ambient gas are observed. It is revealed that, in the mbar pressure regime and at intermediate temperature conditions (500-700 °C), steam acts as an oxidant for nickel but has a dual oxidant/reductant function for doped ceria.

  18. Facile preparation of nickel/carbonized wood nanocomposite for environmentally friendly supercapacitor electrodes

    PubMed Central

    Yaddanapudi, Haritha Sree; Tian, Kun; Teng, Shiang; Tiwari, Ashutosh

    2016-01-01

    We are reporting a facile way to prepare nickel/carbon nanocomposites from wood as a novel electrode material for supercapacitors. The surface morphology and the structure of the as-prepared electrodes were studied by using X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS). The results indicate that after high-temperature carbonization process, the wood is converted into graphitic carbon with nickel nanoparticles uniformly distributed within the three dimensional structure of the wood. Electrochemical characterization such as cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS) and galvanostatic charge-discharge measurements were conducted. These results showed that the introduction of nickel into the carbonized wood improves the specific capacitance and the cyclic stability of the nanocomposite electrode over that of the pure carbonized wood electrode. The composite electrode displayed an enhanced capacitive performance of 3616 F/g at 8 A/g, and showed an excellent capacitance retention after 6000 charge-discharge cycles. These results endow the nickel nanoparticles impregnated carbonized wood with a great potential for future application in supercapacitors. PMID:27651005

  19. 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).

  20. Surfactant-assisted ultrasonic spray pyrolysis of nickel oxide and lithium-doped nickel oxide thin films, toward electrochromic applications

    NASA Astrophysics Data System (ADS)

    Denayer, Jessica; Bister, Geoffroy; Simonis, Priscilla; Colson, Pierre; Maho, Anthony; Aubry, Philippe; Vertruyen, Bénédicte; Henrist, Catherine; Lardot, Véronique; Cambier, Francis; Cloots, Rudi

    2014-12-01

    Lithium-doped nickel oxide and undoped nickel oxide thin films have been deposited on FTO/glass substrates by a surfactant-assisted ultrasonic spray pyrolysis. The addition of polyethylene glycol in the sprayed solution has led to improved uniformity and reduced light scattering compared to films made without surfactant. Furthermore, the presence of lithium ions in NiO films has resulted in improved electrochromic performances (coloration contrast and efficiency), but with a slight decrease of the electrochromic switching kinetics.

  1. Synthesis of bacteria promoted reduced graphene oxide-nickel sulfide networks for advanced supercapacitors.

    PubMed

    Zhang, Haiming; Yu, Xinzhi; Guo, Di; Qu, Baihua; Zhang, Ming; Li, Qiuhong; Wang, Taihong

    2013-08-14

    Supercapacitors with potential high power are useful and have attracted much attention recently. Graphene-based composites have been demonstrated to be promising electrode materials for supercapacitors with enhanced properties. To improve the performance of graphene-based composites further and realize their synthesis with large scale, we report a green approach to synthesize bacteria-reduced graphene oxide-nickel sulfide (BGNS) networks. By using Bacillus subtilis as spacers, we deposited reduced graphene oxide/Ni3S2 nanoparticle composites with submillimeter pores directly onto substrate by a binder-free electrostatic spray approach to form BGNS networks. Their electrochemical capacitor performance was evaluated. Compared with stacked reduced graphene oxide-nickel sulfide (GNS) prepared without the aid of bacteria, BGNS with unique nm-μm structure exhibited a higher specific capacitance of about 1424 F g(-1) at a current density of 0.75 A g(-1). About 67.5% of the capacitance was retained as the current density increased from 0.75 to 15 A g(-1). At a current density of 75 A g(-1), a specific capacitance of 406 F g(-1) could still remain. The results indicate that the reduced graphene oxide-nickel sulfide network promoted by bacteria is a promising electrode material for supercapacitors.

  2. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

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

    2008-01-01

    An uncycled electrode for a non-aqueous lithium electrochemical cell including a lithium metal oxide having the formula Li.sub.(2+2x)/(2+x)M'.sub.2x/(2+x)M.sub.(2-2x)/(2+x)O.sub.2-.delta., in which 0.ltoreq.x<1 and .delta. is less than 0.2, and in which M is a non-lithium metal ion with an average trivalent oxidation state selected from two or more of the first row transition metals or lighter metal elements in the periodic table, and M' is one or more ions with an average tetravalent oxidation state selected from the first and second row transition metal elements and Sn. Methods of preconditioning the electrodes are disclosed as are electrochemical cells and batteries containing the electrodes.

  3. Oxygen Evolution Catalyzed by Nickel-Iron Oxide Nanocrystals with a Nonequilibrium Phase.

    PubMed

    Bau, Jeremy A; Luber, Erik J; Buriak, Jillian M

    2015-09-09

    Mixed nickel-iron oxides are of great interest as electrocatalysts for the oxygen evolution reaction (OER), the kinetically challenging half-reaction required for the generation of hydrogen gas from water via electrolysis. Previously, we had reported the synthesis of single crystal, soluble nickel-iron oxide nanoparticles over a wide range of nickel:iron compositions, with a metastable cubic rock salt phase ([Ni,Fe]O) that can be isolated despite the low solubility of iron in cubic nickel oxide at ambient temperatures. Here, activity for OER was examined, catalyzed by these [Ni,Fe]O nanoparticles integrated with indium tin oxide (ITO) electrodes. Because the as-prepared [Ni,Fe]O nanoparticles are oleate-capped, the surface ligands needed to be removed to induce adherence to the ITO substrate, and to enable charge transfer and contact with water to enable OER catalysis. Two different approaches were taken to reduce or eliminate the coverage of oleate ligands in these films: UV irradiation (254 nm) and air plasma. UV irradiation proved to lead to better results in terms of stable and OER-active films at pH 13. Kinetic analysis revealed that the Tafel slopes of these nanoparticle [Ni,Fe]O OER electrodes were limited by the electrochemical surface area and were found to be within the range of 30 to 50 mV/decade. Across the four compositions of Ni:Fe studied, from 24:76 to 88:12, the observed overpotential at 10 mA/cm2 for the OER in basic conditions decreased from 0.47 to 0.30 V as the proportion of nickel increased from 24% to 88%.

  4. Nickel oxide thin film from electrodeposited nickel sulfide thin film: peroxide sensing and photo-decomposition of phenol.

    PubMed

    Jana, Sumanta; Samai, Subhasis; Mitra, Bibhas C; Bera, Pulakesh; Mondal, Anup

    2014-09-14

    A novel non-enzymatic peroxide sensor has been constructed by using nickel oxide (NiO) thin films as sensing material, which were prepared by a two-step process: (i) electrodeposition of nickel sulfide (NiS) and (ii) thermal air oxidation of as-deposited NiS to NiO. The resultant material is highly porous and comprises interconnected nanofibers. UV-Vis spectroscopy, FTIR spectroscopy, X-ray photoelectron spectroscopy (XPS), X-ray diffraction (XRD) and field-emission scanning electron microscopy (FESEM) were used for a complete characterization of nanostructured NiO thin films. Cyclic voltammetry study shows that NiO/ITO electrode facilitates the oxidation of hydrogen peroxide and exhibits excellent catalytic activity towards its sensing. The amperometric study of NiO/ITO was carried out to determine the sensitivity, linear range, detection limit of the proposed sensor. The sensor exhibits prominent electrocatalytic activity toward the oxidation of H2O2 with a wide linear range and a low detection limit. The possible use of the synthesized NiO thin films as an effective photocatalyst for the decomposition of phenol is also discussed.

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

    NASA Astrophysics Data System (ADS)

    Cetinkaya, T.; Uysal, M.; Akbulut, H.

    2015-04-01

    In this study, nickel plated silicon powders were produced using an electroless deposition process. The nickel content on the surface of silicon powders was changed by using different concentrations of NiCl2 in the plating bath. The surface morphology of the produced Ni plated composite powders was characterized using scanning electron microscopy (SEM). Energy dispersive spectroscopy (EDS) was used to determine the elemental surface composition of the composites. X-ray diffraction (XRD) analysis was performed to investigate the structure of the nickel plated silicon powders. Electrochemical cycling test of the nickel plated silicon electrodes were performed at a constant current of 100 mA/g in CR2016 test cells. In order to investigate electrochemical reactions of the nickel plated silicon powders with electrolyte, cyclic voltammetry test was performed at a scan rate of 0.1 mV/s. Among the used concentrations, the nickel plated silicon electrode produced using 40 g/L NiCl2 had a 246 mAh/g discharge capacity after 30 cycles.

  6. Effects of the mode of storage on the capacity fading of the sintered nickel electrodes

    NASA Technical Reports Server (NTRS)

    Vyes, B.; Bernhardt, M. P.

    1982-01-01

    A systematic investigation of the effect of temperature and two conditions of storage, shortened and open circuit, on the capacity fading of sintered nickel electrodes in NiCd batteries was conducted. All testing was done on sintered electrodes in flooded cells. Cycling tests to measure the capacity were performed at room temperature. The capacity out to one volt, a capacity useful for satellite applications. Test results indicated that: the shortened electrode showed a higher rate of loss than the open circuit electrodes; there was an increase in both modes with an increase in temperature; there was a loss of capacity with time of storage; a general degradation was observed as a function of time; shortened electrodes showed a higher end of charge than the open circuit ones; and at room temperature there was a lower loss in the open circuit electrode than in the shortened one.

  7. Nanostructured solid oxide fuel cell electrodes

    NASA Astrophysics Data System (ADS)

    Sholklapper, Tal Zvi

    The ability of Solid Oxide Fuel Cells (SOFC) to directly and efficiently convert the chemical energy in hydrocarbon fuels to electricity places the technology in a unique and exciting position to play a significant role in the clean energy revolution. In order to make SOFC technology cost competitive with existing technologies, the operating temperatures have been decreased to the range where costly ceramic components may be substituted with inexpensive metal components within the cell and stack design. However, a number of issues have arisen due to this decrease in temperature: decreased electrolyte ionic conductivity, cathode reaction rate limitations, and a decrease in anode contaminant tolerance. While the decrease in electrolyte ionic conductivities has been countered by decreasing the electrolyte thickness, the electrode limitations have remained a more difficult problem. Nanostructuring SOFC electrodes addresses the major electrode issues. The infiltration method used in this dissertation to produce nanostructure SOFC electrodes creates a connected network of nanoparticles; since the method allows for the incorporation of the nanoparticles after electrode backbone formation, previously incompatible advanced electrocatalysts can be infiltrated providing electronic conductivity and electrocatalysis within well-formed electrolyte backbones. Furthermore, the method is used to significantly enhance the conventional electrode design by adding secondary electrocatalysts. Performance enhancement and improved anode contamination tolerance are demonstrated in each of the electrodes. Additionally, cell processing and the infiltration method developed in conjunction with this dissertation are reviewed.

  8. Nanostructured Solid Oxide Fuel Cell Electrodes

    SciTech Connect

    Sholklapper, Tal Zvi

    2007-01-01

    The ability of Solid Oxide Fuel Cells (SOFC) to directly and efficiently convert the chemical energy in hydrocarbon fuels to electricity places the technology in a unique and exciting position to play a significant role in the clean energy revolution. In order to make SOFC technology cost competitive with existing technologies, the operating temperatures have been decreased to the range where costly ceramic components may be substituted with inexpensive metal components within the cell and stack design. However, a number of issues have arisen due to this decrease in temperature: decreased electrolyte ionic conductivity, cathode reaction rate limitations, and a decrease in anode contaminant tolerance. While the decrease in electrolyte ionic conductivities has been countered by decreasing the electrolyte thickness, the electrode limitations have remained a more difficult problem. Nanostructuring SOFC electrodes addresses the major electrode issues. The infiltration method used in this dissertation to produce nanostructure SOFC electrodes creates a connected network of nanoparticles; since the method allows for the incorporation of the nanoparticles after electrode backbone formation, previously incompatible advanced electrocatalysts can be infiltrated providing electronic conductivity and electrocatalysis within well-formed electrolyte backbones. Furthermore, the method is used to significantly enhance the conventional electrode design by adding secondary electrocatalysts. Performance enhancement and improved anode contamination tolerance are demonstrated in each of the electrodes. Additionally, cell processing and the infiltration method developed in conjunction with this dissertation are reviewed.

  9. Manganese oxide composite electrodes for lithium batteries

    DOEpatents

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

    2009-12-22

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

  10. A novel sensor for cephalosporins based on electrocatalytic oxidation by poly(o-anisidine)/SDS/Ni modified carbon paste electrode.

    PubMed

    Ojani, Reza; Raoof, Jahan-Bakhsh; Zamani, Saeed

    2010-06-15

    In this work for first time, the electrocatalytic oxidations of some cephalosporins were carried out by poly(o-anisidine)/SDS/Ni modified carbon paste electrode using cyclic voltammetry, chronoamperometry and chronocoulometry methods. At first, poly(o-anisidine) was formed by cyclic voltammetry in monomer solution containing sodium dodesyl sulfate (SDS), on carbon paste electrode surface. Then, Ni(II) ions were incorporated to electrode by immersion of the polymeric modified electrode having amine group in 0.1molL(-1) Ni(II) ion solution. A good redox behavior was observed for the Ni(OH)(2)/NiOOH couple on the surface of this electrode. Cephalosporins were successfully oxidized on the surface of this nickel ions dispersed poly(o-anisidine) modified carbon paste electrode. The electrocatalytic oxidation peak currents of cephalosporins were linearly dependent on their concentration. Electrode was successfully applied to determine cephalosporins in pharmaceutical preparations.

  11. Molybdenum oxide electrodes for thermoelectric generators

    DOEpatents

    Schmatz, Duane J.

    1989-01-01

    The invention is directed to a composite article suitable for use in thermoelectric generators. The article comprises a thin film comprising molybdenum oxide as an electrode deposited by physical deposition techniques onto solid electrolyte. The invention is also directed to the method of making same.

  12. Low temperature formation of electrode having electrically conductive metal oxide surface

    DOEpatents

    Anders, Simone; Anders, Andre; Brown, Ian G.; McLarnon, Frank R.; Kong, Fanping

    1998-01-01

    A low temperature process is disclosed for forming metal suboxides on substrates by cathodic arc deposition by either controlling the pressure of the oxygen present in the deposition chamber, or by controlling the density of the metal flux, or by a combination of such adjustments, to thereby control the ratio of oxide to metal in the deposited metal suboxide coating. The density of the metal flux may, in turn, be adjusted by controlling the discharge current of the arc, by adjusting the pulse length (duration of on cycle) of the arc, and by adjusting the frequency of the arc, or any combination of these parameters. In a preferred embodiment, a low temperature process is disclosed for forming an electrically conductive metal suboxide, such as, for example, an electrically conductive suboxide of titanium, on an electrode surface, such as the surface of a nickel oxide electrode, by such cathodic arc deposition and control of the deposition parameters. In the preferred embodiment, the process results in a titanium suboxide-coated nickel oxide electrode exhibiting reduced parasitic evolution of oxygen during charging of a cell made using such an electrode as the positive electrode, as well as exhibiting high oxygen overpotential, resulting in suppression of oxygen evolution at the electrode at full charge of the cell.

  13. Layered method of electrode for solid oxide electrochemical cells

    DOEpatents

    Jensen, Russell R.

    1991-07-30

    A process for fabricating a fuel electrode comprising: slurry dipping to form layers which are structurally graded from all or mostly all stabilized zirconia at a first layer, to an outer most layer of substantially all metal powder, such an nickel. Higher performaance fuel electrodes may be achieved if sinter active stabilized zirconia doped for electronic conductivity is used.

  14. Primary Water SCC Understanding and Characterization Through Fundamental Testing in the Vicinity of the Nickel/Nickel Oxide Phase Transition

    SciTech Connect

    D.S. Morton; S.A. Attanasio; G.A. Young

    2001-05-08

    This paper quantifies the nickel alloy stress corrosion crack growth rate (SCCGR) dissolved hydrogen level functionality. SCCGR has been observed to exhibit a maximum in proximity to the nickel/nickel oxide phase transition. The dissolved hydrogen level SCCGR dependency has been quantified in a phenomenological model in terms of the stability of nickel oxide not the dissolved hydrogen level. The observed SCCGR dependency has been extended to lower temperatures through the developed model and Contact Electrical Resistance (CER) measurements of the nickel/nickel oxide phase transition. Understanding obtained from this hydrogen level SCC functionality and complementary SCC subprocesses test results is discussed. Specifically, the possible SCC fundamental subprocesses of corrosion kinetics, hydrogen permeation and pickup have also been measured for nickel alloys. Secondary Ion Mass Spectroscopy (SIMS) analysis has been performed on SCCGR specimens tested in heavy water (D{sub 2}O).

  15. Electrochemical synthesis of nickel-aluminium oxide system from metals obtained by ore processing

    NASA Astrophysics Data System (ADS)

    Korobochkin, V. V.; Usoltseva, N. V.; Shorokhov, K. G.; Popova, E. V.

    2015-11-01

    Separate and combined electrochemical oxidation of aluminium and nickel has been conducted by alternating current of industrial frequency. Concentration increase of electrolyte solution (sodium chloride) in the range from 3 to 25 wt. % and current density from 0.5 to 1.5 A/cm2 was found to result in the increasing metal oxidation rate, excluding aluminium oxidation which oxidation rate is independent of the electrolyte solution concentration. At the current density of 1.5 A/cm2 the products of separate oxidation of nickel and aluminium are nickel oxyhydroxides, nickel hydroxides and aluminium oxyhydroxide (boehmite), respectively. In addition to these compounds, the nickel-aluminium oxide hydrate is included in the products of nickel and aluminium co-oxidation. Its content grows with the increasing electrolyte solution concentration. Varying the concentration and current density within the limits indicated, the nickel-aluminium oxide system with nickel oxide content from 3 to 10 wt. % is produced.

  16. Copper conducting electrode with nickel as a seed layer for selective emitter crystalline silicon solar cells

    NASA Astrophysics Data System (ADS)

    ur Rehman, Atteq; Shin, Eun Gu; Lee, Soo Hong

    2014-09-01

    In this research, we investigated selective emitter formation with a single-step photolithography process having a metallization scheme composed of nickel/copper metal stacks. The nickel seed layers were deposited by applying the electroless deposition process while copper was formed by light induced electro-plating arrangements as the main conducting electrode. The electroless deposition of nickel, along with a sintering process, was employed to create a diffusion barrier between copper and silicon. The nickel metal stack below the copper-conducting electrode also helped in lowering the sheet resistance and improving the contact adhesion. The nickel used as a seed layer was successfully demonstrated in the fabrication of a homogeneous 60 Ω/□ emitter and selective emitter cells. Lower series resistances of 0.165 Ω and 0.253 Ω were achieved for the selective emitter and the homogeneous emitter cells, respectively. The best cell efficiency of 18.37% for the selective emitter solar cell was achieved, with average cell efficiencies of 18.17% and 17.3% for the selective emitter and the homogeneous emitter cells, respectively. An approximate efficiency increase of about 0.8% was recorded for the selective emitter solar cells.

  17. Reference electrode for strong oxidizing acid solutions

    DOEpatents

    Rigdon, Lester P.; Harrar, Jackson E.; Bullock, Sr., Jack C.; McGuire, Raymond R.

    1990-01-01

    A reference electrode for the measurement of the oxidation-reduction potentials of solutions is especially suitable for oxidizing solutions such as highly concentrated and fuming nitric acids, the solutions of nitrogen oxides, N.sub.2 O.sub.4 and N.sub.2 O.sub.5, in nitric acids. The reference electrode is fabricated of entirely inert materials, has a half cell of Pt/Ce(IV)/Ce(III)/70 wt. % HNO.sub.3, and includes a double-junction design with an intermediate solution of 70 wt. % HNO.sub.3. The liquid junctions are made from Corning No. 7930 glass for low resistance and negligible solution leakage.

  18. 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.

  19. Cold fusion by electrolysis in a light water-potassium carbonate solution with a nickel electrode

    SciTech Connect

    Notoya, Reiko )

    1993-09-01

    The evolution of a large amount of heat, unexplainable by ordinary chemical reactions, was observed in an electrolytic cell with a nickel cathode and a platinum anode in a potassium carbonate-light water solution. The nickel cathode had a specially designed porous structure, based on fundamental knowledge concerning the active hydrogen electrode in alkaline solutions. An increase in the concentration of calcium ions was observed in the electrolyte, which seems to be the result of potassium-hydrogen cold fusion. 5 refs., 4 figs.

  20. Solution processed nickel oxide anodes for organic photovoltaic devices

    SciTech Connect

    Mustafa, Bestoon; Griffin, Jonathan; Alsulami, Abdullah S.; Lidzey, David G.; Buckley, Alastair R.

    2014-02-10

    Nickel oxide thin films have been prepared from a nickel acetylacetonate (Ni(acac)) precursor for use in bulk heterojunction organic photovoltaic devices. The conversion of Ni(acac) to NiO{sub x} has been investigated. Oxygen plasma treatment of the NiO layer after annealing at 400 °C affords solar cell efficiencies of 5.2%. Photoelectron spectroscopy shows that high temperature annealing converts the Ni(acac) to a reduced form of nickel oxide. Additional oxygen plasma treatment further oxidizes the surface layers and deepens the NiO work function from 4.7 eV for the annealed film, to 5.0 eV allowing for efficient hole extraction at the organic interface.

  1. Nanostructured nickel electrodes using the Tobacco mosaic virus for microbattery applications

    NASA Astrophysics Data System (ADS)

    Gerasopoulos, Konstantinos; McCarthy, Matthew; Royston, Elizabeth; Culver, James N.; Ghodssi, Reza

    2008-10-01

    The development of nanostructured nickel-zinc microbatteries utilizing the Tobacco mosaic virus (TMV) is presented in this paper. The TMV is a high aspect ratio cylindrical plant virus which has been used to increase the active electrode area in MEMS-fabricated batteries. Genetically modifying the virus to display multiple metal binding sites allows for electroless nickel deposition and self-assembly of these nanostructures onto gold surfaces. This work focuses on integrating the TMV deposition and coating process into standard MEMS fabrication techniques as well as characterizing nickel-zinc microbatteries based on this technology. Using a microfluidic packaging scheme, devices with and without TMV structures have been characterized. The TMV modified devices demonstrated charge-discharge operation up to 30 cycles reaching a capacity of 4.45 µAh cm-2 and exhibited a six-fold increase in capacity during the initial cycle compared to planar electrode geometries. The effect of the electrode gap has been investigated, and a two-fold increase in capacity is observed for an approximately equivalent decrease in electrode spacing.

  2. Electrochemical dechlorination of chloroform in neutral aqueous solution on palladium/foam-nickel and palladium/polymeric pyrrole film/foam-nickel electrodes.

    PubMed

    Sun, Zhirong; Li, Baohua; Hu, Xiang; Shi, Min; Hou, Qingnan; Peng, Yongzhen

    2008-01-01

    Electrochemical dechlorination of chloroform in neutral aqueous solution was investigated using palladium-loaded electrodes at ambient temperature. Palladium/foam-nickel (Pd/foam-Ni) and palladium/polymeric pyrrole film/foam-nickel (Pd/PPy/foam-Ni) composite electrodes which provided catalytic surface for reductive dechlorination of chloroform in aqueous solution were prepared using an electrodepositing method. Scanning electron microscope (SEM) micrographs showed that polymeric pyrrole film modified the electrode-surface characteristics and resulted in the uniform dispersion of needle-shaped palladium particles on foam-Ni supporting electrode. The experimental results of dechlorination indicated that the removal efficiency of chloroform and current efficiency in neutral aqueous solution on Pd/PPy/foam-Ni electrode could be up to 36.8% and 33.0% at dechlorination current of 0.1 mA and dechlorination time of 180 min, which is much higher than that of Pd/foam-Ni electrode.

  3. Lithium metal oxide electrodes for lithium batteries

    DOEpatents

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

    2010-06-08

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

  4. Manganese oxide composite electrodes for lithium batteries

    DOEpatents

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

    2007-12-04

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

  5. Oxidation stages of Ni electrodes in solid oxide fuel cell environments.

    PubMed

    El Gabaly, Farid; McCarty, Kevin F; Bluhm, Hendrik; McDaniel, Anthony H

    2013-06-07

    Nickel is the most commonly used anode for solid-oxide fuel cells (SOFC) due to its fast kinetics and low price. A leading cause of degradation in Ni electrodes is oxidation. Here we use operando ambient-pressure X-ray photoelectron spectroscopy (XPS) to chemically characterize the Ni electrode of a fuel cell anode during oxidation in a H2/H2O atmosphere. We find three different stages of Ni oxidation in the model SOFC. In the first two stages, the Ni exposed to the gas remains metallic but the Ni at the interface with the zirconia electrolyte is oxidized. In the third oxidation stage, we find that Ni transforms to NiOOH, a phase not previously considered in the SOFC literature. We show that the transformation between Ni and NiOOH is reversible and is initiated at the Ni/gas interface. In addition we find that NiOOH stores charge, as evidenced by the stable discharge plateau (voltage) measured as this oxyhydroxide phase reduces to metallic Ni.

  6. Initial capacity conditioning on electrochemical nickel hydroxide electrodes

    NASA Technical Reports Server (NTRS)

    Fritts, D. H.

    1981-01-01

    Conditioning is the initial cycling where cell capacity is usually unstable. The causes of the initial capacity build were examined. Gridless electrodes were fabricated to ensure mechanical homogeneity, so that a strain measured in one direction would be typical of a strain measured in the other directions. Plate hardness was also determined. These two parameters stabilize together.

  7. 75 FR 70583 - Cobalt Lithium Manganese Nickel Oxide; Withdrawal of Significant New Use Rule

    Federal Register 2010, 2011, 2012, 2013, 2014

    2010-11-18

    ... AGENCY 40 CFR Parts 9 and 721 RIN 2070-AB27 Cobalt Lithium Manganese Nickel Oxide; Withdrawal of... Control Act (TSCA) for the chemical substance identified as cobalt lithium manganese nickel oxide (CAS No... cobalt lithium manganese nickel oxide (PMN P-04-269; CAS No. 182442-95-1) at 40 CFR 721.10201 because the...

  8. 40 CFR 721.5315 - Nickel, cobalt mixed metal oxide (generic).

    Code of Federal Regulations, 2014 CFR

    2014-07-01

    ... 40 Protection of Environment 31 2014-07-01 2014-07-01 false Nickel, cobalt mixed metal oxide... Specific Chemical Substances § 721.5315 Nickel, cobalt mixed metal oxide (generic). (a) Chemical substance... nickel, cobalt mixed metal oxide. (PMN P-02-90) is subject to reporting under this section for...

  9. 40 CFR 721.5315 - Nickel, cobalt mixed metal oxide (generic).

    Code of Federal Regulations, 2011 CFR

    2011-07-01

    ... 40 Protection of Environment 31 2011-07-01 2011-07-01 false Nickel, cobalt mixed metal oxide... Specific Chemical Substances § 721.5315 Nickel, cobalt mixed metal oxide (generic). (a) Chemical substance... nickel, cobalt mixed metal oxide. (PMN P-02-90) is subject to reporting under this section for...

  10. 40 CFR 721.5315 - Nickel, cobalt mixed metal oxide (generic).

    Code of Federal Regulations, 2013 CFR

    2013-07-01

    ... 40 Protection of Environment 32 2013-07-01 2013-07-01 false Nickel, cobalt mixed metal oxide... Specific Chemical Substances § 721.5315 Nickel, cobalt mixed metal oxide (generic). (a) Chemical substance... nickel, cobalt mixed metal oxide. (PMN P-02-90) is subject to reporting under this section for...

  11. 40 CFR 721.5315 - Nickel, cobalt mixed metal oxide (generic).

    Code of Federal Regulations, 2010 CFR

    2010-07-01

    ... 40 Protection of Environment 30 2010-07-01 2010-07-01 false Nickel, cobalt mixed metal oxide... Specific Chemical Substances § 721.5315 Nickel, cobalt mixed metal oxide (generic). (a) Chemical substance... nickel, cobalt mixed metal oxide. (PMN P-02-90) is subject to reporting under this section for...

  12. 40 CFR 721.5315 - Nickel, cobalt mixed metal oxide (generic).

    Code of Federal Regulations, 2012 CFR

    2012-07-01

    ... 40 Protection of Environment 32 2012-07-01 2012-07-01 false Nickel, cobalt mixed metal oxide... Specific Chemical Substances § 721.5315 Nickel, cobalt mixed metal oxide (generic). (a) Chemical substance... nickel, cobalt mixed metal oxide. (PMN P-02-90) is subject to reporting under this section for...

  13. Performance of fuel cells with proton-conducting ceria-based composite electrolyte and nickel-based electrodes

    NASA Astrophysics Data System (ADS)

    Huang, Jianbing; Mao, Zongqiang; Liu, Zhixiang; Wang, Cheng

    A ceria-based composite electrolyte with the composition of Ce 0.8Sm 0.2O 1.9 (SDC)-30 wt.% (2Li 2CO 3:1Na 2CO 3) is developed for intermediate temperature fuel cells (ITFCs). Two kinds of SDC powders are used to prepare the composite electrolytes, which are synthesized by oxalate coprecipitation process and glycine-nitrate process, respectively, and denoted as SDC(OCP) and SDC(GNP). Based on each composite electrolyte, two single cells with the electrolyte thickness of 0.3 and 0.5 mm are fabricated by dry-pressing technique, using nickel oxide as anode and lithiated nickel oxide as cathode, respectively. With H 2 as fuel and air as oxidant, all the four cells exhibit excellent performances at 400-600 °C, which can be attributed to the highly ionic conducting electrolyte and the compatible electrodes. The cell performance is influenced by the SDC morphology and the electrolyte thickness. More interestingly, such composite electrolytes are found to be proton conductors at intermediate temperature range for the first time since almost all water is observed at the cathode side during fuel cell operation for all cases. The unusual transport property, excellent cell performance and potential low cost make this kind of composite material a good candidate electrolyte for future cost-effective ITFCs.

  14. Non-enzymatic amperometric glucose biosensor based on nickel hexacyanoferrate nanoparticle film modified electrodes.

    PubMed

    Wang, Xiaoyan; Zhang, Yun; Banks, Craig E; Chen, Qiyuan; Ji, Xiaobo

    2010-07-01

    A non-enzymatic amperometric glucose biosensor based on the modification of functional nickel hexacyanoferrate nanoparticles was prepared via electrochemical deposition. The electrochemical deposition of the nickel hexacyanoferrate nanoparticles was obtained by potential cycling in a solution containing nickel (II) and hexacyanoferrate (III) producing a modified surface with a high degree of uniformity. The modified electrode is exemplified towards the non-enzymatic sensing of glucose where using cyclic voltammetry and amperometry, low micro-molar up to milli-molar glucose concentrations are readily detectable. The non-enzymatic sensing of glucose also shows a modest selectivity over ascorbic acid. This platform offers a novel route for glucose sensors with wide analytical applications.

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

    NASA Technical Reports Server (NTRS)

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

    1991-01-01

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

  16. Zinc oxide interdigitated electrode for biosensor application

    NASA Astrophysics Data System (ADS)

    Sin L., L.; Arshad, M. K. Md.; Fathil, M. F. M.; Adzhri, R.; M. Nuzaihan M., N.; Ruslinda, A. R.; Gopinath, Subash C. B.; Hashim, U.

    2016-07-01

    In biosensors, zinc oxide (ZnO) thin film plays a crucial role in term of stability, sensitivity, biocompatibility and low cost. Interdigitated electrode (IDE) design is one of the device architecture in biosensor for label free, stability and sensitivity. In this paper, we discuss the fabrication of zinc oxide deposited on the IDE as a transducer for sensing of biomolecule. The formation of APTES had increase the performance of the surface functionalization..Furthermore we extend the discuss on the surface functionalization process which is utilized for probe attachment onto the surface of biosensor through surface immobilization process, thus enables the sensing of biomolecules for biosensor application.

  17. 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##

  18. Potassium Sodium Niobate-Based Lead-Free Piezoelectric Multilayer Ceramics Co-Fired with Nickel Electrodes

    PubMed Central

    Kawada, Shinichiro; Hayashi, Hiroyuki; Ishii, Hideki; Kimura, Masahiko; Ando, Akira; Omiya, Suetake; Kubodera, Noriyuki

    2015-01-01

    Although lead-free piezoelectric ceramics have been extensively studied, many problems must still be overcome before they are suitable for practical use. One of the main problems is fabricating a multilayer structure, and one solution attracting growing interest is the use of lead-free multilayer piezoelectric ceramics. The paper reviews work that has been done by the authors on lead-free alkali niobate-based multilayer piezoelectric ceramics co-fired with nickel inner electrodes. Nickel inner electrodes have many advantages, such as high electromigration resistance, high interfacial strength with ceramics, and greater cost effectiveness than silver palladium inner electrodes. However, widely used lead zirconate titanate-based ceramics cannot be co-fired with nickel inner electrodes, and silver palladium inner electrodes are usually used for lead zirconate titanate-based piezoelectric ceramics. A possible alternative is lead-free ceramics co-fired with nickel inner electrodes. We have thus been developing lead-free alkali niobate-based multilayer ceramics co-fired with nickel inner electrodes. The normalized electric-field-induced thickness strain (Smax/Emax) of a representative alkali niobate-based multilayer ceramic structure with nickel inner electrodes was 360 pm/V, where Smax denotes the maximum strain and Emax denotes the maximum electric field. This value is about half that for the lead zirconate titanate-based ceramics that are widely used. However, a comparable value can be obtained by stacking more ceramic layers with smaller thicknesses. In the paper, the compositional design and process used to co-fire lead-free ceramics with nickel inner electrodes are introduced, and their piezoelectric properties and reliabilities are shown. Recent advances are introduced, and future development is discussed. PMID:28793646

  19. Potassium Sodium Niobate-Based Lead-Free Piezoelectric Multilayer Ceramics Co-Fired with Nickel Electrodes.

    PubMed

    Kawada, Shinichiro; Hayashi, Hiroyuki; Ishii, Hideki; Kimura, Masahiko; Ando, Akira; Omiya, Suetake; Kubodera, Noriyuki

    2015-11-03

    Although lead-free piezoelectric ceramics have been extensively studied, many problems must still be overcome before they are suitable for practical use. One of the main problems is fabricating a multilayer structure, and one solution attracting growing interest is the use of lead-free multilayer piezoelectric ceramics. The paper reviews work that has been done by the authors on lead-free alkali niobate-based multilayer piezoelectric ceramics co-fired with nickel inner electrodes. Nickel inner electrodes have many advantages, such as high electromigration resistance, high interfacial strength with ceramics, and greater cost effectiveness than silver palladium inner electrodes. However, widely used lead zirconate titanate-based ceramics cannot be co-fired with nickel inner electrodes, and silver palladium inner electrodes are usually used for lead zirconate titanate-based piezoelectric ceramics. A possible alternative is lead-free ceramics co-fired with nickel inner electrodes. We have thus been developing lead-free alkali niobate-based multilayer ceramics co-fired with nickel inner electrodes. The normalized electric-field-induced thickness strain (Smax/Emax) of a representative alkali niobate-based multilayer ceramic structure with nickel inner electrodes was 360 pm/V, where Smax denotes the maximum strain and Emax denotes the maximum electric field. This value is about half that for the lead zirconate titanate-based ceramics that are widely used. However, a comparable value can be obtained by stacking more ceramic layers with smaller thicknesses. In the paper, the compositional design and process used to co-fire lead-free ceramics with nickel inner electrodes are introduced, and their piezoelectric properties and reliabilities are shown. Recent advances are introduced, and future development is discussed.

  20. Preparation and supercapacitor application of the single crystal nickel hydroxide and oxide nanosheets

    SciTech Connect

    Li, Qing; Ni, Haifang; Cai, Yun; Cai, Xiaoyan; Liu, Yongjun; Chen, Gang; Fan, Li-Zhen; Wang, Yude

    2013-09-01

    Graphical abstract: The nickel hydroxide and nickel oxide nanosheets prepared using CTAB at room temperature exhibit a high specific capacitance, prompt charge/discharge rate. - Highlights: • The nickel hydroxide nanosheets were prepared using CTAB at room temperature. • Ni(OH){sub 2} nanosheet can be successfully converted to NiO nanosheet via calcination. • The NiO nanosheet has a specific capacitance of 388 F g{sup −1} at 5 A g{sup −1} in KOH solution. • Anneal temperature impacts capacitive properties as electrode. - Abstract: The single crystalline Ni(OH){sub 2} nanosheets were synthesized by a simple chemical precipitation method using nickel chloride as precursors and ammonia as precipitating agent. The Ni(OH){sub 2} nanosheets were successfully converted to NiO nanosheets via calcination under appropriate conditions. Analytical methods such as X-ray diffraction (XRD) spectra, scanning electron microscopy (SEM), transmission electron microscopy (TEM), high-resolution TEM (HRTEM), and Fourier transformed infrared (FTIR) spectra were employed to characterize the morphology and microstructure of the final products. The experimental results revealed that Ni(OH){sub 2} nanosheets were shape-preserved transformed to NiO nanosheets at 250 °C for 24 h. Ni(OH){sub 2} and NiO nanosheets were directly functionalized as supercapacitor electrodes for potential energy storage applications, whose charge–discharge properties, electrochemical impedance spectra, cyclic voltammetry, and cycle performance were examined. The experimental results show that the single-crystalline NiO nanosheets are a promising candidate for the supercapacitor electrode. They exhibit a high specific capacitance, prompt charge/discharge rate.

  1. XAS study of lithium nickel oxide

    NASA Astrophysics Data System (ADS)

    Rougier, A.; Chadwick, A. V.; Delmas, C.

    1995-05-01

    LiNiO2 crystallizes in the rhombohedral symmetry with the layered α-NaFeO2 type structure. On the contrary of the homologous NaNiO2 phase, it does not exhibit macroscopic structural distortion due to the Jahn-Teller effect of low spin trivalent nickel ions. The EXAFS study shows that in fact all NiO6 octahedra are distorted (two long and four short Nisbnd O distances).

  2. Oxidation resistant iron and nickel alloys for high temperature use

    NASA Technical Reports Server (NTRS)

    Hill, V. L.; Misra, S. K.; Wheaton, H. L.

    1970-01-01

    Iron-base and nickel-base alloys exhibit good oxidation resistance and improved ductility with addition of small amounts of yttrium, tantalum /or hafnium/, and thorium. They can be used in applications above the operating temperatures of the superalloys, if high strength materials are not required.

  3. Submicron nickel-oxide-gold tunnel diode detectors for rectennas

    NASA Technical Reports Server (NTRS)

    Hoofring, A. B.; Kapoor, V. J.; Krawczonek, W.

    1989-01-01

    The characteristics of a metal-oxide-metal (MOM) tunnel diode made of nickel, nickel-oxide, and gold, designed and fabricated by standard integrated circuit technology for use in FIR rectennas, are presented. The MOM tunnel diode was formed by overlapping a 0.8-micron-wide layer of 1000-A of nickel, which was oxidized to form a thin layer of nickel oxide, with a 1500 A-thick layer of gold. The dc current-voltage characteristics of the MOM diode showed that the current dependence on voltage was linear about zero bias up to a bias of about 70 mV. The maximum detection of a low-level signal (10-mV ac) was determined to be at a dc voltage of 70 mV across the MOM diode. The rectified output signal due to a chopped 10.6-micron CO2 laser incident upon the rectenna device was found to increase with dc bias, with a maximum value of 1000 nV for a junction bias of 100 mV at room temperature.

  4. Ex-situ tracking solid oxide cell electrode microstructural evolution in a redox cycle by high resolution ptychographic nanotomography

    NASA Astrophysics Data System (ADS)

    De Angelis, Salvatore; Jørgensen, Peter Stanley; Esposito, Vincenzo; Tsai, Esther Hsiao Rho; Holler, Mirko; Kreka, Kosova; Abdellahi, Ebtisam; Bowen, Jacob R.

    2017-08-01

    For solid oxide fuel and electrolysis cells, precise tracking of 3D microstructural change in the electrodes during operation is considered critical to understand the complex relationship between electrode microstructure and performance. Here, for the first time, we report a significant step towards this aim by visualizing a complete redox cycle in a solid oxide cell (SOC) electrode. The experiment demonstrates synchrotron-based ptychography as a method of imaging SOC electrodes, providing an unprecedented combination of 3D image quality and spatial resolution among non-destructive imaging techniques. Spatially registered 3D reconstructions of the same location in the electrode clearly show the evolution of the microstructure from the pristine state to the oxidized state and to the reduced state. A complete mechanical destruction of the zirconia backbone is observed via grain boundary fracture, the nickel and pore networks undergo major reorganization and the formation of internal voids is observed in the nickel-oxide particles after the oxidation. These observations are discussed in terms of reaction kinetics, electrode mechanical stress and the consequences of redox cycling on electrode performance.

  5. In situ fabrication of nickel based oxide on nitrogen-doped graphene for high electrochemical performance supercapacitors

    NASA Astrophysics Data System (ADS)

    Pan, Denghui; Zhang, Mingmei; Wang, Ying; Yan, Zaoxue; Jing, Junjie; Xie, Jimin

    2017-10-01

    In this article, we synthesize Ni(OH)2 homogeneous grown on nitrogen-doped graphene (Ni(OH)2/NG), subsequently, small and uniform nickel oxide nanoparticle (NiO/NG) is also successfully obtained through tube furnace calcination method. The high specific capacitance of the NiO/NG electrode can reach to 1314.1 F/g at a charge and discharge current density of 2 A/g, meanwhile the specific capacitance of Ni(OH)2/NG electrode is also 1350 F/g. The capacitance of NiO/NG can remain 93.7% of the maximum value after 1000 cycles, while the Ni(OH)2/NG electrode losses 16.9% of the initial capacitance after 1000 cycles. It can be attributed to nickel hydroxide instability during charge-discharge cycles.

  6. Electrochemical degradation of carbaryl on oxide electrodes.

    PubMed

    Miwa, D W; Malpass, G R P; Machado, S A S; Motheo, A J

    2006-10-01

    This paper presents the study of a prospective electrochemical treatment system for the pesticide carbaryl. Three different dimensionally stable anodes were employed (Ti/Ru0.3 Ti0.7 O2, Ti/Ru0.3 Sn0.7 O2 and Ti/Ir0.3 Ti0.7 O2) and the effect of current density (10, 20, 40 and 60 mA cm(-2)) and supporting electrolyte (0.1 mol L(-1) NaCl and 0.033 mol L(-1) H2SO4) is discussed. All the electrodes present a low level of carbaryl and total organic carbon removal in H2SO4, even at highly positive potentials, indicating that the application of current is not, in itself, sufficient to promote effective oxidation of the pesticide and its products. However, in the presence of NaCl all the electrodes used present rapid diminishing of the carbaryl and total organic carbon content, thus suggesting enhanced activity. The results demonstrate the participation of partially oxidised Cl- species at the electrode surface, which act as an intermediate in the electron transfer between the pesticide molecule and the electrode. Thus, under such conditions, the feasibility of the electrochemical route for the treatment (total or partial) of waste that contains carbaryl is evident.

  7. On the Nickel Hydroxide Electrode. I. On Nickel (II) Hydroxide Hydrate,

    DTIC Science & Technology

    1980-10-27

    preparations. The nickel content is calculated as Ni(OH)2, and the remainder of the total water as water of hydration. The pycnometric density is...determined with anhydrous petroleum (b. p. 150-200*) as the sealing liquid. The pycnometric density of a well crystallized anhydrous P-Ni(OH)2 , prepared by...blue, and P-Co(OH)2 is pink. Table 2. Ni(OH)2 Zn(OH)2 H20 Ni,Zn(OH)2 H20 Pycnometric density % % % Mol Mol g/cm3 5 10 29.30 12,34 1 0.75 - 61,50

  8. Synthesis of nickel nanoparticles supported on metal oxides using electroless plating: controlling the dispersion and size of nickel nanoparticles.

    PubMed

    Wu, Zhijie; Ge, Shaohui; Zhang, Minghui; Li, Wei; Tao, Keyi

    2009-02-15

    Nickel nanoparticles supported on metal oxides were prepared by a modified electroless nickel-plating method. The process and mechanism of electroless plating were studied by changing the active metal (Ag) loading, acidity, and surface area of metal oxides and were characterized by UV-vis spectroscopy, transmission electron microscopy, scanning electron microscopy, and H(2) chemisorption. The results showed that the dispersion of nickel nanoparticles was dependent on the interface reaction between the metal oxide and the plating solution or the active metal and the plating solution. The Ag loading and acidity of the metal oxide mainly affected the interface reaction to change the dispersion of nickel nanoparticles. The use of ultrasonic waves and microwaves and the change of solvents from water to ethylene glycol in the electroless plating could affect the dispersion and size of nickel nanoparticles.

  9. A semi theoretical approach of the second plateau appearing during the discharge of aged nickel oxyhydroxide electrodes

    NASA Astrophysics Data System (ADS)

    Mancier, V.; Willmann, P.; Metrot, A.

    A semi theoretical explanation of the appearance of a second plateau during the discharge of overcharged nickel oxyhydroxide electrodes (NOHE) is proposed, based on transmission line models of the charge-discharge processes of the active matter. The model takes into account the double electronic and protonic conduction involved in nickel II α and β or nickel III β and γ phases: electrons and protons reach the transformation front inside the matter through the less resistive paths. The secondary plateau may occur when a resistive layer of β(II) isolates the transformation front from the nickel electron sink.

  10. NO.sub.x sensing devices having conductive oxide electrodes

    DOEpatents

    Montgomery, Frederick C.; West, David L.; Armstrong, Timothy R.; Maxey, Lonnie C.

    2010-03-16

    A NO.sub.x sensing device includes at least one pair of spaced electrodes, at least one of which is made of a conductive oxide, and an oxygen-ion conducting material in bridging electrical communication with the electrodes.

  11. Synthesis, spectroscopic and electrochemical performance of pasted β-nickel hydroxide electrode in alkaline electrolyte.

    PubMed

    Shruthi, B; Bheema Raju, V; Madhu, B J

    2015-01-25

    β-Nickel hydroxide (β-Ni(OH)2) was successfully synthesized using precipitation method. The structure and property of the β-Ni(OH)2 were characterized by X-ray diffraction (XRD), Fourier Transform infra-red (FT-IR), Raman spectra and thermal gravimetric-differential thermal analysis (TG-DTA). The results of the FTIR spectroscopy and TG-DTA studies indicate that the β-Ni(OH)2 contains water molecules and anions. The microstructural and composition studies have been performed using Scanning Electron Microscopy (SEM) and Energy Dispersive X-ray (EDX) analysis. A pasted-type electrode is prepared using β-Ni(OH)2 powder as the active material on a nickel sheet as a current collector. Cyclic voltammetry (CV) and Electrochemical impedance spectroscopy (EIS) studies were performed to evaluate the electrochemical performance of the β-Ni(OH)2 electrode in 6M KOH electrolyte. CV curves showed a pair of strong redox peaks as a result of the Faradaic redox reactions of β-Ni(OH)2. The proton diffusion coefficient (D) for the present β-Ni(OH)2 electrode material is found to be 1.44×10(-12) cm(2) s(-1). Further, electrochemical impedance studies confirmed that the β-Ni(OH)2 electrode reaction processes are diffusion controlled. Copyright © 2014 Elsevier B.V. All rights reserved.

  12. Nickel Oxide, Ceramic Insulated, High Temperature Coating.

    DTIC Science & Technology

    1987-01-27

    coating comprising an MCrAIY layer 22, a ceramic ronments. Aluminide coatings , (a nickel, cobalt, alumi...resistant layered Aluminide and MCrAIY, wherein M is a metal coating as recited in claim 1. wherein the thickness of selected from the group...MCrAIY layer is in the range of: 20% to coating as recitei in claim 17, wherein the thickness of 40% Cr, 5% to 15% AI; 0% to 1% Y; and the balance 55 said aluminide layer is in the range of one to five mils. being M. * 6O

  13. Porous nickel oxide films for electrochemical capacitors

    SciTech Connect

    Liu, K.C.; Anderson, M.A.

    1995-12-31

    NiO/Ni composite thin films consisting of nano-sized particles have been found to perform as good electrodes in electrochemical capacitor applications. These films can provide a specific capacitance of 25--40 F/g. The low cost of raw materials and easy manufacturing process of this system should allow one to produce low-cost electrochemical capacitors.

  14. Flexible, silver nanowire network nickel hydroxide core-shell electrodes for supercapacitors

    NASA Astrophysics Data System (ADS)

    Yuksel, Recep; Coskun, Sahin; Kalay, Yunus Eren; Unalan, Husnu Emrah

    2016-10-01

    We present a novel one-dimensional coaxial architecture composed of silver nanowire (Ag NW) network core and nickel hydroxide (Ni(OH)2) shell for the realization of coaxial nanocomposite electrode materials for supercapacitors. Ag NWs are formed conductive networks via spray coating onto polyethylene terephthalate (PET) substrates and Ni(OH)2 is gradually electrodeposited onto the Ag NW network to fabricate core-shell electrodes for supercapacitors. Synergy of highly conductive Ag NWs and high capacitive Ni(OH)2 facilitate ion and electron transport, enhance electrochemical properties and result in a specific capacitance of 1165.2 F g-1 at a current density of 3 A g-1. After 3000 cycles, fabricated nanocomposite electrodes show 93% capacity retention. The rational design explored in this study points out the potential of nanowire based coaxial energy storage devices.

  15. Recrystallization characteristics of oxide dispersion strengthened nickel-base alloys

    NASA Technical Reports Server (NTRS)

    Hotzler, R. K.; Glasgow, T. K.

    1980-01-01

    Electron microscopy was employed to study the process of recrystallization in two oxide dispersion strengthened (ODS) mechanically alloyed nickel-base alloys, MA 754 and MA 6000E. MA 754 contained both fine, uniformly dispersed particles and coarser oxides aligned along the working direction. Hot rolled MA 754 had a grain size of 0.5 microns and high dislocation densities. After partial primary recrystallization, the fine grains transformed to large elongated grains via secondary (or abnormal) grain growth. Extruded and rolled MA 6000E contained equiaxed grains of 0.2 micron diameter. Primary recrystallization occurring during working eliminated virtually all dislocations. Conversion from fine to coarse grains was triggered by gamma prime dissolution; this was also a process of secondary or abnormal grain growth. Comparisons were made to conventional and oxide dispersion strengthened nickel-base alloys.

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

    PubMed

    Nogueira, C A; Margarido, F

    2012-01-01

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

  17. Development of a ceramic powder for use in multilayer capacitors with nickel electrodes

    SciTech Connect

    Chu, M.; Bultitude, J.; Rae, A.; Thompson, I.

    1997-12-31

    The high price of Pd has spurred an increase in activity in base metal usage in MLC capacitors. These have distinct advantages in high layer count, high value parts where high Pd internal electrode systems become uneconomic. Base metal (Nickel) compatible dielectric compositions have been in use for some years. Nickel has achieved predominance of late with the development of X7R materials and the opportunity for high layer count Ni base metal MLCCs to compete with Tantalum capacitors. Concerns about Nickel base metal systems have included MLCC reliability, the sheer difficulty of producing reliable parts, and the high capital costs of base metal furnaces using reducing atmospheres. The systems approach used by TAM and TAM`s partners encompasses equipment, gas atmosphere, binder and electrode as well as ceramic dielectric, as the interactions during the firing cycle, although complex, are easily controlled if the system is considered as a whole. This paper describes the combination of a number of novel technologies which will allow an increase in reliability, ease of processing and a novel approach to firing which will dramatically reduce production costs for X7R MLCCs.

  18. Structural comparison of nickel electrodes and precursor phases

    NASA Technical Reports Server (NTRS)

    Cornilsen, Bahne C.; Shan, Xiaoyin; Loyselle, Patricia

    1989-01-01

    Researchers summarize previous Raman spectroscopic results and discuss important structural differences in the various phases of active mass and active mass precursors. Raman spectra provide unique signatures for these phases, and allow one to distinguish each phase, even when the compound is amorphous to x rays (i.e., does not scatter x rays because of a lack of order and/or small particle size). The structural changes incurred during formation, charge and discharge, cobalt addition, and aging are discussed. The oxidation states and dopant contents are explained in terms of the nonstoichiometric structures.

  19. Selective electrooxidation of uric acid in presence of ascorbic acid at a room temperature ionic liquid/nickel hexacyanoferarrate nanoparticles composite electrode.

    PubMed

    Babu, R Suresh; Prabhu, P; Narayanan, S Sriman

    2011-12-01

    A novel amperometric sensor for the determination of uric acid was fabricated using room temperature ionic liquid and nickel hexacyanoferrate nanoparticle composite which was immobilized on paraffin wax impregnated graphite electrode. The nickel hexacyanoferrate nanoparticle was characterized by UV-vis, X-ray diffraction and field emission scanning electron microscopy. The electrochemical behavior of the modified electrode was investigated in detail by electrochemical impedance spectroscopy, cyclic voltammetry and differential pulse voltammetry. Various experimental parameters influencing the electrochemical behavior of the modified electrode were optimized by varying the supporting electrolyte, scan rate and pH. The apparent electron transfer rate constant (K(s)) and charge transfer coefficient (α) of the modified electrode were found to be 1.358(± 0.02)cm/s and 0.65, respectively from cyclic voltammetry. The sensor exhibited an excellent electrocatalytic activity towards the oxidation of uric acid. The interference from ascorbic acid was easily overcome by coating the modified electrode with PEDOT layer. Under optimal condition, the determination range for uric acid is from 1.0 × 10(-6)M to 2.6 × 10(-3)M and the detection limit was 3.3 × 10(-7)M (3σ). The proposed method has been used for the determination of uric acid in human urine samples. Copyright © 2011 Elsevier B.V. All rights reserved.

  20. Adsorptive stripping voltammetry of nickel with 1-nitroso-2-napthol using a bismuth film electrode.

    PubMed

    Segura, Rodrigo; Pradena, Milenco; Pinto, Deny; Godoy, Fernando; Nagles, Edgar; Arancibia, Verónica

    2011-10-15

    A sensitive procedure is presented for the voltammetric determination of nickel. The procedure involves an adsorptive accumulation of nickel 1-nitroso-2-napthol (NN) complex on a bismuth film electrode prepared ex situ by electrodeposition. The most suitable operating conditions and parameters such as pH, ligand concentration (C(NN)), adsorptive potential (E(ads)), adsorptive time (t(ads)), scan rate and others were selected and the determination of nickel in aqueous solutions using the standard addition method was possible. The adsorbed Ni-NN complex gives a well defined cathodic stripping peak current at -0.70 V, which was used for the determination of nickel in the concentration range of 10.0-70.0 μg L(-1) (pH 7.5; C(NN) 6.5 μmol L(-1); E(ads) -0.30 V; t(ads) 60s) with a detection limit of 0.1 μg L(-1). The relative standard deviation for a solution containing 10.0 μg L(-1) of Ni(II) was 3.5% (n=4). The proposed method was validated determining Ni(II) in certified reference waste water (SPS-WW1) and Certified Reference Water for Trace Elements (TMDA 51.3) with satisfactory results. Then lake water samples were analyzed. Copyright © 2011. Published by Elsevier B.V.

  1. Method for control of edge effects of oxidant electrode

    DOEpatents

    Carr, Peter; Chi, Chen H.

    1980-12-23

    Described is an electrode assembly comprising; a. a porous electrode having a first and second exterior face with a cavity formed in the interior between said exterior faces thereby having first and second interior faces positioned opposite the first and second exterior faces; b. a counter electrode positioned facing each of the first and second exterior faces of the porous electrode; c. means for passing an oxidant through said porous electrode; and d. screening means for blocking the interior face of the porous electrode a greater amount than the blocking of the respective exterior face of the porous electrode, thereby maintaining a differential of oxidant electrode surface between the interior face and the exterior face. The electrode assembly is useful in a metal, halogen, halogen hydrate electrical energy storage device.

  2. Nickel-based layered double hydroxide from guest vanadium oxide anions

    NASA Astrophysics Data System (ADS)

    Park, Hae Woong; Chae, Ji Su; Park, Sun-Min; Kim, Kwang-Bum; Roh, Kwang Chul

    2013-07-01

    The layered double hydroxides (LDHs) are well known for ionic exchange properties to intercalate anionic compound in interlayer region. The Ni/V LDH composite was explored by co-precipitation method. The maximum capacitance of Ni/V LDH composite was 2612 F g-1 at the scan rate 2 mV s-1. As-synthesized Ni/V LDH composite provides a three-dimensional conducting network frame for manifesting electrochemical capacitance. This is because the insertion of vanadium oxide anions (VOx -) into nickel interlayer space between nickel layers is compensated for hydroxyl vacancies during synthesis of lower-pH condition. The network frame makes it possible to promote fast electron transfer for Ni/V LDH composite electrode material and consequently allows the improvement of the electronic conductivity for Ni/V LDH composite electrode material. Thus, the Ni/V LDH composite exhibits high capacitance than β-Ni(OH)2 due to its unique properties, with vanadium oxide anions embedded in the turbostratic structure and shorter diffusion pathway.

  3. Reduced graphite oxide in supercapacitor electrodes.

    PubMed

    Lobato, Belén; Vretenár, Viliam; Kotrusz, Peter; Hulman, Martin; Centeno, Teresa A

    2015-05-15

    The current energy needs have put the focus on highly efficient energy storage systems such as supercapacitors. At present, much attention focuses on graphene-like materials as promising supercapacitor electrodes. Here we show that reduced graphite oxide offers a very interesting potential. Materials obtained by oxidation of natural graphite and subsequent sonication and reduction by hydrazine achieve specific capacitances as high as 170 F/g in H2SO4 and 84F/g in (C2H5)4NBF4/acetonitrile. Although the particle size of the raw graphite has no significant effect on the physico-chemical characteristics of the reduced materials, that exfoliated from smaller particles (<75 μm) result more advantageous for the release of the stored electrical energy. This effect is particularly evident in the aqueous electrolyte. Graphene-like materials may suffer from a drop in their specific surface area upon fabrication of electrodes with features of the existing commercial devices. This should be taken into account for a reliable interpretation of their performance in supercapacitors.

  4. Thin film synthesis of novel electrode materials for solid-oxide fuel cells

    SciTech Connect

    Jankowski, A.F.; Morse, J.D.

    1997-12-01

    Electrode materials for solid-oxide fuel cells are developed using sputter deposition. A thin film anode is formed by co-deposition of nickel and yttria-stabilized zirconia. This approach is suitable for composition grading and the provision of a mixed-conducting interracial layer to the electrolyte layer. Similarly, synthesis of a thin film cathode proceeds by co-deposition of silver and yttria- stabilized zirconia. The sputter deposition of a thin film solid- oxide fuel cell is next demonstrated. The thin film fuel cell microstructure is examined using scanning electron microscopy whereas the cell performance is characterized through current-voltage measurement and corresponding impedance spectroscopy.

  5. Method of electrode fabrication for solid oxide electrochemical cells

    DOEpatents

    Jensen, Russell R.

    1990-01-01

    A process for fabricating cermet electrodes for solid oxide electrochemical cells by sintering is disclosed. First, a porous metal electrode is fabricated on a solid oxide cell, such as a fuel cell by, for example, sintering, and is then infiltrated with a high volume fraction stabilized zirconia suspension. A second sintering step is used to sinter the infiltrated zirconia to a high density in order to more securely attach the electrode to the solid oxide electrolyte of the cell. High performance fuel electrodes can be obtained with this process. Further electrode performance enhancement may be achieved if stabilized zirconia doped with cerium oxide, chromium oxide, titanium oxide, and/or praseodymium oxide for electronic conduction is used.

  6. Method of electrode fabrication for solid oxide electrochemical cells

    DOEpatents

    Jensen, R.R.

    1990-11-20

    A process for fabricating cermet electrodes for solid oxide electrochemical cells by sintering is disclosed. First, a porous metal electrode is fabricated on a solid oxide cell, such as a fuel cell by, for example, sintering, and is then infiltrated with a high volume fraction stabilized zirconia suspension. A second sintering step is used to sinter the infiltrated zirconia to a high density in order to more securely attach the electrode to the solid oxide electrolyte of the cell. High performance fuel electrodes can be obtained with this process. Further electrode performance enhancement may be achieved if stabilized zirconia doped with cerium oxide, chromium oxide, titanium oxide, and/or praseodymium oxide for electronic conduction is used. 5 figs.

  7. Nickel foam-based manganese dioxide-carbon nanotube composite electrodes for electrochemical supercapacitors

    NASA Astrophysics Data System (ADS)

    Li, Jun; Yang, Quan Min; Zhitomirsky, Igor

    Manganese dioxide nanofibers with length ranged from 0.1 to 1 μm and a diameter of about 2-4 nm were prepared by a chemical precipitation method. Composite electrodes for electrochemical supercapacitors were fabricated by impregnation of slurries of the manganese dioxide nanofibers and multiwalled carbon nanotubes (MWCNTs) into porous nickel foam current collectors. In the composite electrodes, MWCNT formed a secondary conductivity network within the nickel foam cells. Obtained composite electrodes, containing 0-20 wt.% MWCNT with total mass loading of 40 mg cm -2, showed a capacitive behavior in the 0.1-0.5 M Na 2SO 4 solutions. The highest specific capacitance (SC) of 155 F g -1 was obtained at a scan rate of 2 mV s -1 in the 0.5 M Na 2SO 4 solutions. The SC increased with increasing MWCNT content in the composite materials and increasing Na 2SO 4 concentration in the solutions and decreased with increasing scan rate.

  8. Reactively sputtered nickel nitride as electrocatalytic counter electrode for dye- and quantum dot-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Soo Kang, Jin; Park, Min-Ah; Kim, Jae-Yup; Ha Park, Sun; Young Chung, Dong; Yu, Seung-Ho; Kim, Jin; Park, Jongwoo; Choi, Jung-Woo; Jae Lee, Kyung; Jeong, Juwon; Jae Ko, Min; Ahn, Kwang-Soon; Sung, Yung-Eun

    2015-05-01

    Nickel nitride electrodes were prepared by reactive sputtering of nickel under a N2 atmosphere at room temperature for application in mesoscopic dye- or quantum dot- sensitized solar cells. This facile and reliable method led to the formation of a Ni2N film with a cauliflower-like nanostructure and tetrahedral crystal lattice. The prepared nickel nitride electrodes exhibited an excellent chemical stability toward both iodide and polysulfide redox electrolytes. Compared to conventional Pt electrodes, the nickel nitride electrodes showed an inferior electrocatalytic activity for the iodide redox electrolyte; however, it displayed a considerably superior electrocatalytic activity for the polysulfide redox electrolyte. As a result, compared to dye-sensitized solar cells (DSCs), with a conversion efficiency (η) = 7.62%, and CdSe-based quantum dot-sensitized solar cells (QDSCs, η = 2.01%) employing Pt counter electrodes (CEs), the nickel nitride CEs exhibited a lower conversion efficiency (η = 3.75%) when applied to DSCs, but an enhanced conversion efficiency (η = 2.80%) when applied to CdSe-based QDSCs.

  9. Cermet electrode

    DOEpatents

    Maskalick, Nicholas J.

    1988-08-30

    Disclosed is a cermet electrode consisting of metal particles of nickel, cobalt, iron, or alloys or mixtures thereof immobilized by zirconia stabilized in cubic form which contains discrete deposits of about 0.1 to about 5% by weight of praseodymium, dysprosium, terbium, or a mixture thereof. The solid oxide electrode can be made by covering a substrate with particles of nickel, cobalt, iron, or mixtures thereof, growing a stabilized zirconia solid oxide skeleton around the particles thereby immobilizing them, contacting the skeleton with a compound of praseodymium, dysprosium, terbium, or a mixture thereof, and heating the skeleton to a temperature of at least 500.degree. C. The electrode can also be made by preparing a slurry of nickel, cobalt, iron, or mixture and a compound of praseodymium, dysprosium, terbium, or a mixture thereof, depositing the slurry on a substrate, heating the slurry to dryness, and growing a stabilized zirconia skeleton around the metal particles.

  10. Gas-phase reactions of nickel and nickel oxide clusters with nitrogen dioxide. 4: Continued kinetic and mechanistic investigation of nickel cluster reactions with NO{sub 2} gases

    SciTech Connect

    Vann, W.D.; Castleman, A.W. Jr.

    1999-02-18

    Results of investigations of the gas-phase reactions of nickel and nickel oxide ions with NO{sub 2} are reported in this final part of a four-part series. A fast flow reactor-quadrupole mass spectrometer system coupled with a laser vaporization source is used to study reactions of nickel and nickel oxide cluster ions with nitrogen dioxide. Pseudo-first-order biomolecular rate constants for the reactions of NO{sub 2} with nickel and nickel oxide cluster cations and anions are reported. The product distributions indicate that several different reaction mechanisms occur between NO{sub 2} and various sizes of nickel and nickel oxide cluster ions. The reaction processes are mainly oxidation of the nickel clusters and NO{sub 2} addition. Finally, a detailed comparison is made between these reactions and previously reported ones with nitric oxide and oxygen.

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

    SciTech Connect

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

    2014-10-15

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

  12. Evolution of Grain Structure in Nickel Oxide Scales,

    DTIC Science & Technology

    1986-11-01

    examined by Parallel and Transverse Cross-Section Trans- sion Electron Microscopy and Scanning Electron Microscopy-. Text-. e coefficients were found...CONTENTS Page No. 1. INTRODUCTION 1 2. EXPERIMENTAL METHOD 3 2.1 Coupon Preparation and Oxidation 3 2.2 Transverse and Parallel TEM Specimen Preparation...fracture section through scale formed on nickel at 10000C for 18 hours in 1 atm. 02 ( Coupon 48). (iAi) ZLWST1ATIONS (Continued) fig. 14 Grain boundary

  13. Size-dependent magnetic properties of branchlike nickel oxide nanocrystals

    NASA Astrophysics Data System (ADS)

    Liu, Dan; Li, Dongsheng; Yang, Deren

    2017-01-01

    Branchlike nickel oxide nanocrystals with narrow size distribution are obtained by a solution growth method. The size-dependent of magnetic properties of the nickel oxides were investigated. The results of magnetic characterization indicate that the NiO nanocrystals with size below 12.8 nm show very weak ferromagnetic state at room temperature due to the uncompensated spins. Both of the average blocking temperature (Tb) and the irreversible temperature (Tirr) increase with the increase of nanoparticle sizes, while both the remnant magnetization and the coercivity at 300 K increase with the decrease of the particle sizes. Moreover, the disappearance of two-magnon (2M) band and redshift of one-phonon longitudinal (1LO) and two-phonon LO in vibrational properties due to size reduction are observed. Compared to the one with the spherical morphological, it is also found that nano-structured nickel oxides with the branchlike morphology have larger remnant magnetization and the coercivity at 5 K due to their larger surface-to-volume ratio and greater degree of broken symmetry at the surface or the higher proportion of broken bonds.

  14. Controlled synthesis of size-tunable nickel and nickel oxide nanoparticles using water-in-oil microemulsions

    NASA Astrophysics Data System (ADS)

    Kumar, Ajeet; Saxena, Amit; De, Arnab; Shankar, Ravi; Mozumdar, Subho

    2013-06-01

    Industrial demands have generated a growing need to synthesize pure metal and metal-oxide nanoparticles of a desired size. We report a novel and convenient method for the synthesis of spherical, size tunable, well dispersed, stable nickel and nickel oxide nanoparticles by reduction of nickel nitrate at room temperature in a TX-100/n-hexanol/cyclohexane/water system by a reverse microemulsion route. We determined that reduction with alkaline sodium borohydrate in nitrogen atmosphere leads to the formation of nickel nanoparticles, while the use of hydrazine hydrate in aerobic conditions leads to the formation of nickel oxide nanoparticles. The influence of several reaction parameters on the size of nickel and nickel oxide nanoparticles were evaluated in detail. It was found that the size can be easily controlled either by changing the molar ratio of water to surfactant or by simply altering the concentration of the reducing agent. The morphology and structure of the nanoparticles were characterized by quasi-elastic light scattering (QELS), transmission electron microscopy (TEM), x-ray diffraction (XRD), electron diffraction analysis (EDA) and energy dispersive x-ray (EDX) spectroscopy. The results show that synthesized nanoparticles are of high purity and have an average size distribution of 5-100 nm. The nanoparticles prepared by our simple methodology have been successfully used for catalyzing various chemical reactions.

  15. TOF MS Investigation of Nickel Oxide CVD

    NASA Astrophysics Data System (ADS)

    Kondrateva, Anastasia S.; Mishin, Maxim V.; Alexandrov, Sergey E.

    2017-08-01

    NiO layers were deposited by metal-organic chemical vapor deposition using bis-(ethylcyclopentadienyl) nickel (EtCp)2Ni and oxygen or ozone. As a continuation of kinetic study of NiO MOCVD the gas-phase, transformations of (EtCp)2Ni were studied in the temperature range of 380-830 K. Time of reactions corresponding to the residence time of the gas stream in hot zone of the reactor was about 0.1 s under conditions studied. The interaction of (EtCp)2Ni with oxygen started at 450 K and its conversion rate reached the maximum at 700 K. The interaction of (EtCp)2Ni with ozone started at 400 K and its conversion rate reached the maximum at 600 K. Transformations of the gas phase with the temperature in the reaction zone were studied, the model reaction schemes illustrating (EtCp)2Ni transformations in the reaction systems containing oxygen and ozone have developed. In the reaction system (EtCp)2Ni-O2-Ar the main gas-phase products at 380-500 K were CO, CO2, HCO, C2H5OH, CpCOOH, and CpO. Formation of the C2H2O, C3H4O, and C5H8O was found at 630-830 K. The same gas-phase species, (C4H3O)2Ni and dialdehydes was formed in the reaction system (EtCp)2Ni-O3-O2-Ar. [Figure not available: see fulltext.

  16. Free-standing nickel oxide nanoflake arrays: synthesis and application for highly sensitive non-enzymatic glucose sensors.

    PubMed

    Wang, Gongming; Lu, Xihong; Zhai, Teng; Ling, Yichuan; Wang, Hanyu; Tong, Yexiang; Li, Yat

    2012-05-21

    We report a seed-mediated hydrothermal growth of free-standing nickel hydroxide [Ni(OH)(2)] and nickel oxide (NiO) nanoflake arrays and their implementation as electrodes for non-enzymatic glucose sensors. Ni(OH)(2) nanoflakes were converted into porous NiO nanoflakes upon thermal annealing in air at temperatures of 300 °C or above. NiO nanoflake-arrayed sensors achieve an excellent glucose sensitivity of ∼8500 μA cm(-2) mM(-1) and a low detection limit of 1.2 μM glucose at an applied bias of 0.5 V vs. Ag/AgCl. The fabrication of the nanoflake electrode avoids the use of polymer binders representing additional advantage over the conventional powder based glucose sensors. Furthermore, they show good specificity to glucose in the presence of ascorbic acid, d-lactose and d-fructose.

  17. Nickel hydroxide/cobalt-ferrite magnetic nanocatalyst for alcohol oxidation.

    PubMed

    Bhat, Pooja B; Inam, Fawad; Bhat, Badekai Ramachandra

    2014-08-11

    A magnetically separable, active nickel hydroxide (Brønsted base) coated nanocobalt ferrite catalyst has been developed for oxidation of alcohols. High surface area was achieved by tuning the particle size with surfactant. The surface area of 120.94 m2 g(-1) has been achieved for the coated nanocobalt ferrite. Improved catalytic activity and selectivity were obtained by synergistic effect of transition metal hydroxide (basic hydroxide) on nanocobalt ferrite. The nanocatalyst oxidizes primary and secondary alcohols efficiently (87%) to corresponding carbonyls in good yields.

  18. Vanadium oxide electrode synthesized by electroless deposition for electrochemical capacitors

    NASA Astrophysics Data System (ADS)

    Wu, Haoran; Lian, Keryn

    2014-12-01

    A thin film vanadium oxide electrode was synthesized by a simple electroless deposition method. Surface and structural analyses revealed that the deposited oxide is a mixture of amorphous V2O5 and VO2. Electrochemical characterizations of the synthesized vanadium oxide showed capacitive behavior with good cycle life. The electroless deposition of vanadium oxide is inexpensive, easy to process, and environmentally benign, offering a promising route for electrode development for electrochemical capacitors.

  19. Serum levels of protein oxidation products in patients with nickel allergy.

    PubMed

    Gangemi, Sebastiano; Ricciardi, Luisa; Minciullo, Paola Lucia; Cristani, Mariateresa; Saitta, Salvatore; Chirafisi, Joselita; Spatari, Giovanna; Santoro, Giusy; Saija, Antonella

    2009-01-01

    Nickel sensitization can not only induce allergic contact dermatitis (ACD), but also can induce an overlapping disease referred to as "systemic nickel allergy syndrome" (SNAS), characterized by urticaria/angioedema and gastrointestinal symptoms correlated to the ingestion of nickel-containing foods. This study was designed to determine if oxidative stress occurs in patients with nickel allergy. Thirty-one female patients (mean age 31.26 + 13.04 years, range 16-64 years) with confirmed nickel CD underwent oral nickel challenge because of clinically suspected SNAS; serum concentrations of protein carbonyl groups (PCGs) and nitrosylated proteins (NPs; biomarkers of oxidative stress) were measured before and after oral nickel challenge as well as in healthy female controls. Twenty-three of these 31 patients were diagnosed with SNAS because they had a positive reaction to the oral nickel challenge, and 8 patients had no reaction and therefore were classified as patients with contact nickel allergy only. Although both nickel-allergic patients and controls presented similar serum levels of PCGs, NP values in nickel-allergic patients appeared higher than in controls and tended to decrease after the challenge; furthermore, serum levels of NPs in patients affected by SNAS were higher (although not significantly) than in patients with nickel ACD only. The involvement of specific biomarkers of oxidative stress such as NPs and the lack of involvement of other biomarkers such as PCGs may help to better understand the alteration of the redox homeostasis occurring in nickel ACD and particularly in SNAS.

  20. Strongly improved electrochemical cycling durability by adding iridium to electrochromic nickel oxide films.

    PubMed

    Wen, Rui-Tao; Niklasson, Gunnar A; Granqvist, Claes G

    2015-05-13

    Anodically colored nickel oxide (NiO) thin films are of much interest as counter electrodes in tungsten oxide based electrochromic devices such as "smart windows" for energy-efficient buildings. However, NiO films are prone to suffering severe charge density degradation upon prolonged electrochemical cycling, which can lead to insufficient device lifetime. Therefore, a means to improve the durability of NiO-based films is an important challenge at present. Here we report that the incorporation of a modest amount of iridium into NiO films [Ir/(Ir + Ni) = 7.6 atom %] leads to remarkable durability, exceeding 10000 cycles in a lithium-conducting electrolyte, along with significantly improved optical modulation during extended cycling. Structure characterization showed that the face-centered-cubic-type NiO structure remained after iridium addition. Moreover, the crystallinity of these films was enhanced upon electrochemical cycling.

  1. Inhomogeneous distribution of chemical species in lithium nickel oxide cathode of lithium ion battery

    NASA Astrophysics Data System (ADS)

    Uenoyama, T.; Miyahara, R.; Katayama, M.; Inada, Y.

    2016-05-01

    The spatial distribution of the oxidation state for the nickel species in the LiNiO2 cathode was analyzed by means of the in-situ XAFS imaging technique during the charging and discharging processes. The inhomogeneous reaction for the LiNiO2 cathode was observed under the operating condition. The pattern in the 2-dimensional map of the oxidation state of the active material in the discharging process was similar to that in the charging process. It means that the areas preceding the discharging reaction agree with the areas delaying the charging reaction. It was suggested that the diffusion of Li+ was restricted by the surface product of the LiNiO2 electrode, and the concentration gradient of Li+ delayed the charging reaction at the reaction channel of the discharging reaction.

  2. Symmetrical, bi-electrode supported solid oxide fuel cell

    NASA Technical Reports Server (NTRS)

    Cable, Thomas L. (Inventor); Sofie, Stephen W. (Inventor)

    2009-01-01

    The present invention is a symmetrical bi-electrode supported solid oxide fuel cell comprising a sintered monolithic framework having graded pore electrode scaffolds that, upon treatment with metal solutions and heat subsequent to sintering, acquire respective anodic and cathodic catalytic activity. The invention is also a method for making such a solid oxide fuel cell. The graded pore structure of the graded pore electrode scaffolds in achieved by a novel freeze casting for YSZ tape.

  3. Improved performance of quantum dot-sensitized solar cells adopting a highly efficient cobalt sulfide/nickel sulfide composite thin film counter electrode

    NASA Astrophysics Data System (ADS)

    Kim, Hee-Je; Kim, Su-Weon; Gopi, Chandu V. V. M.; Kim, Soo-Kyoung; Rao, S. Srinivasa; Jeong, Myeong-Soo

    2014-12-01

    Cobalt sulfide (CoS), nickel sulfide (NiS), and cobalt sulfide/nickel sulfide (CoS/NiS) were deposited onto fluorine-doped tin oxide (FTO) substrate using a facile chemical bath deposition method and utilized as counter electrodes (CEs) for polysulfide redox reactions in CdS/CdSe quantum dot-sensitized solar cells (QDSSCs). The thickness of 750 nm and 695 nm are optimized for NiS and CoS electrodes to prepare the CoS/NiS CE. Compared to a platinum (Pt) electrode, the CoS, NiS, and composite CoS/NiS electrodes provide higher electrocatalytic activity and lower charge-transfer resistance. The combination of a QDSSC with composite CoS/NiS CE shows an improved power conversion efficiency of 3.40% under the illumination of one sun (100 mW cm-2), which is higher than the CoS (2.53%), NiS (2.61%), and Pt (1.47%) CEs. This enhancement is mainly attributed to the NiS nanoparticles deposited on CoS film, due to which the composite structure exhibits a lower charge transfer resistance (7.61 Ω) at the interface of the CE and the electrolyte, along with superior electrochemical catalytic ability. This is well supported by the cyclic voltammetry, electrochemical impedance spectroscopy, and Tafel polarization measurements.

  4. NICKEL HYDROXIDES

    SciTech Connect

    MCBREEN,J.

    1997-11-01

    Nickel hydroxides have been used as the active material in the positive electrodes of several alkaline batteries for over a century. These materials continue to attract a lot of attention because of the commercial importance of nickel-cadmium and nickel-metal hydride batteries. This review gives a brief overview of the structure of nickel hydroxide battery electrodes and a more detailed review of the solid state chemistry and electrochemistry of the electrode materials. Emphasis is on work done since 1989.

  5. Free-standing nickel oxide nanoflake arrays: synthesis and application for highly sensitive non-enzymatic glucose sensors

    NASA Astrophysics Data System (ADS)

    Wang, Gongming; Lu, Xihong; Zhai, Teng; Ling, Yichuan; Wang, Hanyu; Tong, Yexiang; Li, Yat

    2012-05-01

    We report a seed-mediated hydrothermal growth of free-standing nickel hydroxide [Ni(OH)2] and nickel oxide (NiO) nanoflake arrays and their implementation as electrodes for non-enzymatic glucose sensors. Ni(OH)2 nanoflakes were converted into porous NiO nanoflakes upon thermal annealing in air at temperatures of 300 °C or above. NiO nanoflake-arrayed sensors achieve an excellent glucose sensitivity of ~8500 μA cm-2 mM-1 and a low detection limit of 1.2 μM glucose at an applied bias of 0.5 V vs. Ag/AgCl. The fabrication of the nanoflake electrode avoids the use of polymer binders representing additional advantage over the conventional powder based glucose sensors. Furthermore, they show good specificity to glucose in the presence of ascorbic acid, d-lactose and d-fructose.We report a seed-mediated hydrothermal growth of free-standing nickel hydroxide [Ni(OH)2] and nickel oxide (NiO) nanoflake arrays and their implementation as electrodes for non-enzymatic glucose sensors. Ni(OH)2 nanoflakes were converted into porous NiO nanoflakes upon thermal annealing in air at temperatures of 300 °C or above. NiO nanoflake-arrayed sensors achieve an excellent glucose sensitivity of ~8500 μA cm-2 mM-1 and a low detection limit of 1.2 μM glucose at an applied bias of 0.5 V vs. Ag/AgCl. The fabrication of the nanoflake electrode avoids the use of polymer binders representing additional advantage over the conventional powder based glucose sensors. Furthermore, they show good specificity to glucose in the presence of ascorbic acid, d-lactose and d-fructose. Electronic supplementary information (ESI) available: Electrochemical characterization and TGA analysis. See DOI: 10.1039/c2nr30302g

  6. Reduction of Nickel Oxide with Ethanol

    NASA Astrophysics Data System (ADS)

    Coskun, F.; Cetinkaya, S.; Eroglu, S.

    2017-02-01

    This work aims to investigate the reduction behavior of NiO powder by ethanol vapor at 600-1100 K for the reaction times up to 60 min. The products were characterized by mass measurement, x-ray diffraction, and scanning electron microscopy techniques. The reaction of NiO with ethanol essentially consisted of oxide reduction followed by C deposition. At 600 K, significant oxide reduction was attained. Full oxide reduction was observed at 650-1100 K within 10-15 min. At this temperature range, the reduction reaction was controlled by external mass transfer of gaseous species. At the lower temperature range 600-650 K, the reduction rate was sensitive to the temperature change and influenced by the total gas flow rate to a lesser degree. The temperature dependence of C uptake was explained by Boudouard reaction. The results of this study demonstrate that NiO can be completely reduced to Ni by ethanol as predicted by the thermodynamic analysis.

  7. Electrode-assisted catalytic water oxidation by a flavin derivative

    NASA Astrophysics Data System (ADS)

    Mirzakulova, Ekaterina; Khatmullin, Renat; Walpita, Janitha; Corrigan, Thomas; Vargas-Barbosa, Nella M.; Vyas, Shubham; Oottikkal, Shameema; Manzer, Samuel F.; Hadad, Christopher M.; Glusac, Ksenija D.

    2012-10-01

    The success of solar fuel technology relies on the development of efficient catalysts that can oxidize or reduce water. All molecular water-oxidation catalysts reported thus far are transition-metal complexes, however, here we report catalytic water oxidation to give oxygen by a fully organic compound, the N(5)-ethylflavinium ion, Et-Fl+. Evolution of oxygen was detected during bulk electrolysis of aqueous Et-Fl+ solutions at several potentials above +1.9 V versus normal hydrogen electrode. The catalysis was found to occur on glassy carbon and platinum working electrodes, but no catalysis was observed on fluoride-doped tin-oxide electrodes. Based on spectroelectrochemical results and preliminary calculations with density functional theory, one possible mechanistic route is proposed in which the oxygen evolution occurs from a peroxide intermediate formed between the oxidized flavin pseudobase and the oxidized carbon electrode. These findings offer an organic alternative to the traditional water-oxidation catalysts based on transition metals.

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

    PubMed Central

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

    2016-01-01

    Nickel metal hydride (Ni-MH) batteries have demonstrated key technology advantages for applications in new-energy vehicles, which play an important role in reducing greenhouse gas emissions and the world’s dependence on fossil fuels. However, the poor high-rate dischargeability of the negative electrode materials—hydrogen storage alloys (HSAs) limits applications of Ni-MH batteries in high-power fields due to large polarization. Here we design a hybrid electrode by integrating HSAs with a current collector of three-dimensional bicontinuous nanoporous Ni. The electrode shows enhanced high-rate dischargeability with the capacity retention rate reaching 44.6% at a discharge current density of 3000 mA g−1, which is 2.4 times that of bare HSAs (18.8%). Such a unique hybrid architecture not only enhances charge transfer between nanoporous Ni and HSAs, but also facilitates rapid diffusion of hydrogen atoms in HSAs. The developed HSAs/nanoporous metals hybrid structures exhibit great potential to be candidates as electrodes in high-performance Ni-MH batteries towards applications in new-energy vehicles. PMID:27270184

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

    PubMed

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

    2016-06-07

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

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

    NASA Astrophysics Data System (ADS)

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

    2016-06-01

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

  11. Microwave-assisted synthesis of metal oxide/hydroxide composite electrodes for high power supercapacitors - A review

    NASA Astrophysics Data System (ADS)

    Faraji, Soheila; Ani, Farid Nasir

    2014-10-01

    Electrochemical capacitors (ECs), also known as pseudocapacitors or supercapacitors (SCs), is receiving great attention for its potential applications in electric and hybrid electric vehicles because of their ability to store energy, alongside with the advantage of delivering the stored energy much more rapidly than batteries, namely power density. To become primary devices for power supply, supercapacitors must be developed further to improve their ability to deliver high energy and power simultaneously. In this concern, a lot of effort is devoted to the investigation of pseudocapacitive transition-metal-based oxides/hydroxides such as ruthenium oxide, manganese oxide, cobalt oxide, nickel oxide, cobalt hydroxide, nickel hydroxide, and mixed metal oxides/hydroxides such as nickel cobaltite and nickel-cobalt oxy-hydroxides. This is mainly due to the fact that they can produce much higher specific capacitances than typical carbon-based electric double-layer capacitors and electronically conducting polymers. This review presents supercapacitor performance data of metal oxide thin film electrodes by microwave-assisted as an inexpensive, quick and versatile technique. Supercapacitors have established the specific capacitance (Cs) principles, therefore, it is likely that metal oxide films will continue to play a major role in supercapacitor technology and are expected to considerably increase the capabilities of these devices in near future.

  12. Structural and electrochemical properties of nanostructured nickel silicides by reduction and silicification of high-surface-area nickel oxide

    SciTech Connect

    Chen, Xiao; Zhang, Bingsen; Li, Chuang; Shao, Zhengfeng; Su, Dangsheng; Williams, Christopher T.; Liang, Changhai

    2012-03-15

    Graphical abstract: Nanostructured nickel silicides have been synthesized by reduction and silification of high-surface-area nickel oxide, and exhibited remarkably like-noble metal property, lower electric resistivity, and ferromagnetism at room temperature. Highlights: Black-Right-Pointing-Pointer NiSi{sub x} have been prepared by reduction and silification of high-surface-area NiO. Black-Right-Pointing-Pointer The structure of nickel silicides changed with increasing reaction temperature. Black-Right-Pointing-Pointer Si doping into nickel changed the magnetic properties of metallic nickel. Black-Right-Pointing-Pointer NiSi{sub x} have remarkably lower electric resistivity and like-noble metal property. -- Abstract: Nanostructured nickel silicides have been prepared by reduction and silicification of high-surface-area nickel oxide (145 m{sup 2} g{sup -1}) produced via precipitation. The prepared materials were characterized by nitrogen adsorption, X-ray diffraction, thermal analysis, FT-IR spectroscopy, scanning electron microscopy, transmission electron microscopy, magnetic and electrochemical measurements. The nickel silicide formation involves the following sequence: NiO (cubic) {yields} Ni (cubic) {yields} Ni{sub 2}Si (orthorhombic) {yields} NiSi (orthorhombic) {yields} NiSi{sub 2} (cubic), with particles growing from 13.7 to 21.3 nm. The nickel silicides are ferromagnetic at room temperature, and their saturation magnetization values change drastically with the increase of Si content. Nickel silicides have remarkably low electrical resistivity and noble metal-like properties because of a constriction of the Ni d band and an increase of the electronic density of states. The results suggest that such silicides are promising candidates as inexpensive yet functional materials for applications in electrochemistry as well as catalysis.

  13. 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.

  14. Nickel Diselenide Ultrathin Nanowires Decorated with Amorphous Nickel Oxide Nanoparticles for Enhanced Water Splitting Electrocatalysis.

    PubMed

    Li, Haoyi; Chen, Shuangming; Lin, Haifeng; Xu, Xiaobin; Yang, Haozhou; Song, Li; Wang, Xun

    2017-10-01

    Well-designed hybrid materials based on noble metal-free elements have great potential to generate hydrogen (H2 ) and oxygen (O2 ) sustainably via overall water splitting for developing practical energy-related technologies. Herein, an accessible method is presented to synthesize nickel diselenide (NiSe2 ) ultrathin nanowires decorated with amorphous nickel oxide nanoparticles (NiOx NPs) as multifunctional electrocatalysts (NSWANs) for hydrogen and oxygen evolution reaction (HER and OER). The NSWANs exhibit quite low HER and OER overpotentials of 174 and 295 mV, respectively, holding the current density of 20 mA cm(-2) for 24 h continuous operations in alkaline media. Meanwhile, a cell voltage of 1.547 V at the current density of 10 mA cm(-2) for overall water splitting has been achieved by the NSWANs for the practical application, which could maintain fascinating activity of 20 mA cm(-2) for 72 h without degradation. The decorated NiOx NPs not only prevent the NiSe2 from further oxidation but also expose requisite active sites for electrocatalytic process. It is believed that this study may provide a valuable strategy to design high-efficiency electrocatalysts and expand the applications of selenide-based materials. © 2017 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  15. Evaluation of nickel for positive electrode components in Li-Al/FeS cells

    NASA Astrophysics Data System (ADS)

    Smaga, J. A.; Battles, J. E.

    1982-03-01

    A series of tests were performed to examine the suitability of pure Ni positive electrodes, which have an oxidation potential of 2.2 V, in Li-Al/FeS batteries. A prismatic bicell was employed for the trials with the positive current collector sandwiched between the positive electrode halves, which were covered with Ni screens. The battery was run at 450 C for 31-153 days using different cells. Electrodes were then sectioned, cleaned, measured for thickness, evaluated for reactions, and examined microscopically and metallographically. Largest utilization gains were observed with a LiCl-rich electrolyte. Iron layers, with a thickness up to 6 microns, were found on the Ni components, but were considered too small to display significant life-shortening effects. Cells assembled in less than fully charged conditions showed noticeable intergranular corrosion, a process which was eliminated by using finer Fe particles in the positive electrode mix.

  16. Plasma assisted fabrication of multi-layer graphene/nickel hybrid film as enhanced micro-supercapacitor electrodes

    NASA Astrophysics Data System (ADS)

    Ding, Q.; Li, W. L.; Zhao, W. L.; Wang, J. Y.; Xing, Y. P.; Li, X.; Xue, T.; Qi, W.; Zhang, K. L.; Yang, Z. C.; Zhao, J. S.

    2017-03-01

    A facile synthesis strategy has been developed for fabricating multi-layer graphene/nickel hybrid film as micro-supercapacitor electrodes by using plasma enhanced chemical vapor deposition. The as-presented method is advantageous for rapid graphene growth at relatively low temperature of 650 °C. In addition, after pre-treating for the as-deposited nickel film by using argon plasma bombardment, the surface-to-volume ratio of graphene film on the treated nickel substrate is effectively increased by the increasing of surface roughness. This is demonstrated by the characterization results from transmission electron microscopy, scanning electron microscope and atomic force microscopy. Moreover, the electrochemical performance of the resultant graphene/nickel hybrid film as micro-supercapacitor working electrode was investigated by cyclic voltammetry and galvanostatic charge/discharge measurements. It was found that the increase of the surface-to-volume ratio of graphene/nickel hybrid film improved the specific capacitance of 10 times as the working electrode of micro-supercapacitor. Finally, by using comb columnar shadow mask pattern, the micro-supercapacitor full cell device was fabricated. The electrochemical performance measurements of the micro-supercapacitor devices indicate that the method presented in this study provides an effective way to fabricate micro-supercapacitor device with enhanced energy storage property.

  17. Inert electrode composition having agent for controlling oxide growth on electrode made therefrom

    DOEpatents

    Ray, Siba P.

    1986-01-01

    An improved inert electrode composition is suitable for use as an inert electrode in the production of metals such as aluminum by the electrolytic reduction of metal oxide or metal salt dissolved in a molten salt bath. The composition comprises one or more metal alloys and metal compounds which may include oxides of the metals comprising the alloy. The alloy and metal compounds are interwoven in a network which provides improved electrical conductivity and mechanical strength while preserving the level of chemical inertness necessary for such an electrode to function satisfactorily. The electrode composition further includes a metal compound dopant which will aid in controlling the thickness of a protective oxide layer on at least the bottom portion of an electrode made therefrom during use.

  18. Inert electrode composition having agent for controlling oxide growth on electrode made therefrom

    DOEpatents

    Ray, S.P.

    1986-04-15

    An improved inert electrode composition is suitable for use as an inert electrode in the production of metals such as aluminum by the electrolytic reduction of metal oxide or metal salt dissolved in a molten salt bath. The composition comprises one or more metal alloys and metal compounds which may include oxides of the metals comprising the alloy. The alloy and metal compounds are interwoven in a network which provides improved electrical conductivity and mechanical strength while preserving the level of chemical inertness necessary for such an electrode to function satisfactorily. The electrode composition further includes a metal compound dopant which will aid in controlling the thickness of a protective oxide layer on at least the bottom portion of an electrode made therefrom during use. 12 figs.

  19. Temperature effect on the binder-free nickel copper oxide nanowires with superior supercapacitor performance.

    PubMed

    Zhang, Liuyang; Tang, Chunhua; Gong, Hao

    2014-11-07

    Although the use of nickel oxide in supercapacitor electrodes has been reported extensively, the effect of incorporating copper in the binary compound is not known. Arrays of nickel copper oxide nanowires on the current collector via a simple and industrially compatible route have been successfully synthesized. A systematic study on the effect of temperature is also presented. Strikingly, through conductivity modification and binder-free growth, the as-grown nanowires show high specific capacitance (2.24 F cm(2) at 10 mA; 1955 F g(-1) at 1 mV s(-1)), good rate capability (still 2.18 F cm(2) at 50 mA, 1542 F g(-1) at 50 mV s(-1)), and excellent cycle life (90% after 1000 cycles at a high charging-discharging rate 10 A g(-1)). An asymmetric full cell is then prepared and tested, and very high energy density (30 Wh kg(-1)) is achieved. Ideal capacitive behavior (rectangular shape of cyclic voltammetry) is shown with this tailored architecture of the full cell.

  20. 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.

  1. Nickel Nanofoam/Different Phases of Ordered Mesoporous Carbon Composite Electrodes for Superior Capacitive Energy Storage.

    PubMed

    Lee, Kangsuk; Song, Haeni; Lee, Kwang Hoon; Choi, Soo Hyung; Jang, Jong Hyun; Char, Kookheon; Son, Jeong Gon

    2016-08-31

    Electrochemical energy storage devices based on electric double layer capacitors (EDLCs) have received considerable attention due to their high power density and potential for obtaining improved energy density in comparison to the lithium ion battery. Ordered mesoporous carbon (OMC) is a promising candidate for use as an EDLC electrode because it has a high specific surface area (SSA), providing a wider charge storage space and size-controllable mesopore structure with a long-range order, suppling high accessibility to the electrolyte ions. However, OMCs fabricated using conventional methods have several drawbacks including low electronic conductivity and long ionic diffusion paths in mesopores. We used nickel nanofoam, which has a relatively small pore (sub-100 nm to subμm) network structure, as a current collector. This provides a significantly shortened electronic/ionic current paths and plentiful surface area, enabling stable and close attachment of OMCs without the use of binders. Thus, we present hierarchical binder-free electrode structures based on OMC/Ni nanofoams. These structures give rise to enhanced specific capacitance and a superior rate capability. We also investigated the mesopore structural effect of OMCs on electrolyte transport by comparing the capacitive performances of collapsed lamellar, cylindrical, and spherical mesopore electrodes. The highly ordered and straightly aligned cylindrical OMCs exhibited the highest specific capacitance and the best rate capability.

  2. Pre-oxidized cube textured nickel tapes for YBa 2Cu 3O x coated conductors

    NASA Astrophysics Data System (ADS)

    Eickemeyer, J.; Selbmann, D.; Wendrock, H.; Hühne, R.; Hänisch, J.; Holzapfel, B.

    2007-09-01

    A homogeneous nickel oxide film epitaxially grown on cube textured nickel tapes was prepared as a first buffer layer for subsequent buffer and YBa 2Cu 3O x (YBCO) layer depositions. The nickel oxide film was produced under growth conditions of surface oxidation epitaxy (SOE). The preparation of homogeneous oxide films by SOE with a high texture quality and without disturbing columnar oxide growth succeeded on micro-alloyed nickel tapes. Cerium, yttrium and silver are proven beneficial elements for micro-alloying in this respect. In silver doped metallic substrates, the cube oriented grains were produced with an increased grain aspect ratio, which was transferred to the SOE nickel oxide. Increased transport currents in the YBCO coatings were measured in the longitudinal direction of the tapes, which were coated with an additional system of buffer layers. The critical current density reached up to Jc = 2.35 MA/cm 2 at 77 K in self field.

  3. Negatively strain-dependent electrical resistance of magnetically arranged nickel composites: application to highly stretchable electrodes and stretchable lighting devices.

    PubMed

    Kim, Sangwoo; Byun, Junghwan; Choi, Seongdae; Kim, Donghyun; Kim, Taehoon; Chung, Seungjun; Hong, Yongtaek

    2014-05-21

    A novel property of the negatively strain-dependent electrical resistance change of nickel conductive composites is presented. The composite shows negatively strain-dependent resistance change when magnetically arranged, while most conductive materials show opposite behavior. This negative dependency is utilized to produce highly stretchable electrodes and to demonstrate a new conceptual resolution-sustainable stretchable lighting/display device.

  4. Solid oxide fuel cell electrode characterization and improvement for fuel flexibility and supplemental power production

    NASA Astrophysics Data System (ADS)

    Kellogg, Isaiah Daniel

    2010-03-01

    Solid oxide fuel cells (SOFC) were fabricated and the electrodes tested for their individual catalytic effectiveness in various fuels by exposing each electrode to mixed gas while the opposite electrode was exposed to its respective pure gas. Mixed hydrogen and oxygen gas was successfully utilized as fuel in a single chamber SOFC (SC-SOFC). The conditions at which the porous nickel-yttria-stabilized zirconia (Ni-YSZ) cermet anode performed well did not significantly overlap the conditions at which the La0.8Sr 0.2Fe0.8Co0.2 oxide (LSCF) cathode performed well, but there was significant catalytic activity at both electrodes which increased the open circuit voltage (OCV) beyond that predicted by the Nernst equation. The results of these tests, and future tests of similar format, could be useful in the development of SC-SOFC electrode catalysts. Pyrolytic carbon was used as fuel in a SOFC with a YSZ electrolyte and a bi-layer anode composed of nickel gadolinia-doped ceria (Ni-GDC) and Ni-YSZ. The common problems of bulk shrinkage and emergent porosity in the YSZ layer adjacent to the GDC/YSZ interface were avoided by using an interlayer of porous Ni-YSZ as a buffer anode layer between the electrolyte and the Ni-GDC primary anode. Cells were fabricated from commercially available component powders so that unconventional production methods suggested in the literature were avoided. A cell of similar construction was used with externally applied acetylene flame soot as fuel so that soot captured at the exhaust of a diesel engine could be utilized for secondary power generation in a SOFC while decreasing particulate pollution without the need for filter regeneration.

  5. Nitrogen-doped reduced graphene oxide electrodes for electrochemical supercapacitors.

    PubMed

    Nolan, Hugo; Mendoza-Sanchez, Beatriz; Ashok Kumar, Nanjundan; McEvoy, Niall; O'Brien, Sean; Nicolosi, Valeria; Duesberg, Georg S

    2014-02-14

    Herein we use Nitrogen-doped reduced Graphene Oxide (N-rGO) as the active material in supercapacitor electrodes. Building on a previous work detailing the synthesis of this material, electrodes were fabricated via spray-deposition of aqueous dispersions and the electrochemical charge storage mechanism was investigated. Results indicate that the functionalised graphene displays improved performance compared to non-functionalised graphene. The simplicity of fabrication suggests ease of up-scaling of such electrodes for commercial applications.

  6. Transparent nickel selenide alloy counter electrodes for bifacial dye-sensitized solar cells exceeding 10% efficiency.

    PubMed

    Duan, Yanyan; Tang, Qunwei; He, Benlin; Li, Ru; Yu, Liangmin

    2014-11-07

    In the current work, we report a series of bifacial dye-sensitized solar cells (DSSCs) that provide power conversion efficiencies of more than 10% from bifacial irradiation. The device comprises an N719-sensitized TiO2 anode, a transparent nickel selenide (Ni-Se) alloy counter electrode (CE), and liquid electrolyte containing I(-)/I3(-) redox couples. Because of the high optical transparency, electron conduction ability, electrocatalytic activity of Ni-Se CEs, as well as dye illumination, electron excitation and power conversion efficiency have been remarkably enhanced. Results indicate that incident light from a transparent CE has a compensation effect to the light from the anode. The impressive efficiency along with simple preparation of the cost-effective Ni-Se alloy CEs highlights the potential application of bifacial illumination technique in robust DSSCs.

  7. Surface film formation on nickel electrodes in a propylene carbonate solution at elevated temperatures

    NASA Astrophysics Data System (ADS)

    Mogi, Ryo; Inaba, Minoru; Iriyama, Yasutoshi; Abe, Takeshi; Ogumi, Zempachi

    The effect of temperature on surface film formation on nickel electrode was studied in 1 mol dm -3 bis(perfluoroethylsulfonyl)imide dissolved in propylene carbonate by atomic force microscopy (AFM) and ac impedance spectroscopy. Cyclic voltammetry measurements revealed that electrolyte decomposition reactions are accelerated at elevated temperatures, especially at 60 and 80 °C. In situ AFM measurements showed that the film formation is fast and the resulting surface film is thicker at 80 °C than at room temperature. Furthermore, it was confirmed by ac impedance measurements that the resistance of surface film was very low at elevated temperatures. These results were discussed in relation to superior cycling characteristics of lithium deposition and dissolution at the elevated temperatures.

  8. Surface modification of nickel based alloys for improved oxidation resistance

    SciTech Connect

    Jablonski, Paul D.; Alman, David E.

    2005-02-01

    The present research is aimed at the evaluation of a surface modification treatment to enhance the high temperature stability of nickel-base superalloys. A low Coefficient Thermal Expansion (CTE ~12.5x10-6/°C) alloy based on the composition (in weight %) of Ni-22Mo-12.5Cr was produced by Vacuum Induction Melting and Vacuum Arc Melting and reduced to sheet by conventional thermal-mechanical processing. A surface treatment was devised to enhance the oxidation resistance of the alloys at high temperature. Oxidation tests (in dry and wet air; treated and untreated) were conducted 800°C to evaluate the oxidation resistance of the alloys. The results were compared to the behavior of Haynes 230 (Ni-22Cr) in the treated and untreated conditions. The treatment was not very effective for Haynes 230, as this alloy had similar oxidation behavior in both the treated and untreated conditions. However, the treatment had a significant effect on the behavior of the low CTE alloy. At 800°C, the untreated Ni-12.5Cr alloy was 5 times less oxidation resistant than Haynes 230. However, in the treated condition, the Ni-12.5Cr alloy had comparable oxidation resistance to the Haynes 230 alloy.

  9. Preparation of Sandwich-like NiCo2O4/rGO/NiO Heterostructure on Nickel Foam for High-Performance Supercapacitor Electrodes

    NASA Astrophysics Data System (ADS)

    Li, Delong; Gong, Youning; Wang, Miaosheng; Pan, Chunxu

    2017-04-01

    A kind of sandwich-like NiCo2O4/rGO/NiO heterostructure composite has been successfully anchored on nickel foam substrate via a three-step hydrothermal method with successive annealing treatment. The smart combination of NiCo2O4, reduced graphene oxide (rGO), and NiO nanostructure in the sandwich-like nano architecture shows a promising synergistic effect for supercapacitors with greatly enhanced electrochemical performance. For serving as supercapacitor electrode, the NiCo2O4/rGO/NiO heterostructure materials exhibit remarkable specific capacitance of 2644 mF cm-2 at current density of 1 mA cm-2, and excellent capacitance retentions of 97.5% after 3000 cycles. It is expected that the present heterostructure will be a promising electrode material for high-performance supercapacitors.

  10. A nonstoichiometric structural model to characterize changes in the nickel hydroxide electrode during cycling

    SciTech Connect

    Srinivasan, Venkat; Bahne, C. Cornilsen; Weidner, John W.

    2003-09-15

    Experimental capacities and mass changes are recorded using an electrochemical quartz crystal microbalance during the first 9 charge and discharge cycles of nickel hydroxide thin films cycled in 3.0 weight percent (wt%) potassium hydroxide electrolyte. For the first time, the film capacities have been corrected for the oxygen evolution side reaction, and the data used as input into the point defect-containing structural model to track the changes that occur during short-term cycling. Variations in capacity and mass during formation and charge/discharge cycling are related to changes in the point defect parameters, thus providing a structural origin for the unique experimental variations observed here and often reported in the literature, but previously unexplained. Proton-, potassium-, and water-content vary in the active material during charge/discharge cycling. The observed capacity loss, or ''capacity fade'', is explained by incomplete incorporation of potassium ions in (or near) the nickel vacancy during charge, as additional protons are then allowed to occupy the vacant lattice site. The increase in water content during reduction parallels the expansion of the electrode that is well known during cycling. This result confirms the origin of the swelling phenomenon as being caused by water incorporation. The model and methodology developed in this paper can be used to correlate electrochemical signatures with material chemical structure.

  11. Oxide dispersion strengthening of nickel electrodeposits for microsystem applications.

    SciTech Connect

    Janek, Richard P.; Kotula, Paul Gabriel; Buchheit, Thomas Edward; Michael, R. P.; Goods, Steven Howard

    2003-11-01

    Oxide dispersion strengthened nickel (ODS-Ni) electrodeposits were fabricated to net shape in a nickel sulfamate bath using the LIGA process. A 20 g/l charge of 10 nm Al{sub 2}O{sub 3} powder was suspended in the bath during electrodeposition to produce specimens containing an approximately 0.001-0.02 volume fraction dispersion of the alumina particulate. Mechanical properties are compared to baseline specimens fabricated using an identical sulfamate bath chemistry without the Al{sub 2}O{sub 3} powder charge. Results reveal that the as-deposited ODS-Ni exhibited significantly higher yield strength and ultimate tensile strength than the baseline material. This increase in as-deposited strength is attributed to Orowan strengthening. The ODS-Ni also showed improved retention of room temperature strength after annealing over a range of temperatures up to 600 C. Microscopy revealed that this resistance to anneal softening was due to an inhibition of grain growth in the presence of the oxide dispersion. Nanoindentation measurements revealed that the properties of the dispersion strengthened deposit were uniform through its thickness, even in narrow, high aspect ratio structures. At elevated temperatures, the strength of the ODS-Ni was approximately three times greater than that of the baseline material although with a significant reduction in hot ductility.

  12. Amorphous nickel incorporated tin oxide thin film transistors

    NASA Astrophysics Data System (ADS)

    Yang, Jianwen; Ren, Jinhua; Lin, Dong; Han, Yanbing; Qu, Mingyue; Pi, Shubin; Fu, Ruofan; Zhang, Qun

    2017-09-01

    Nickel as a dopant has been proposed to suppress excess carrier concentration in n-type tin oxide based thin film transistors (TFTs). The influences of Ni content on nickel doped tin oxide (TNO) thin films and their corresponding TFTs were investigated with experimental results showing that the TNO thin films are amorphous. Through the comparison of the transfer characteristic curves of the TNO TFTs with different Ni contents, it was observed that Ni doping is useful to improve the performance of SnO2-based TFTs by suppressing the off-state current and shifting the threshold voltage to 0 V. The amorphous TNO TFT with 3.3 at.% Ni content shows optimum performance, with field effect mobility of 8.4 cm2 V-1 s-1, saturation mobility of 6.8 cm2 V-1 s-1, subthreshold swing value of 0.8 V/decade, and an on-off current ratio of 2.1  ×  107. Nevertheless, the bias stress stability of SnO2-based TFTs deteriorate.

  13. Nickel oxide nanoparticles film produced by dead biomass of filamentous fungus

    PubMed Central

    Salvadori, Marcia Regina; Nascimento, Cláudio Augusto Oller; Corrêa, Benedito

    2014-01-01

    The synthesis of nickel oxide nanoparticles in film form using dead biomass of the filamentous fungus Aspergillus aculeatus as reducing agent represents an environmentally friendly nanotechnological innovation. The optimal conditions and the capacity of dead biomass to uptake and produce nanoparticles were evaluated by analyzing the biosorption of nickel by the fungus. The structural characteristics of the film-forming nickel oxide nanoparticles were analyzed by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). These techniques showed that the nickel oxide nanoparticles had a size of about 5.89 nm and were involved in a protein matrix which probably permitted their organization in film form. The production and uptake of nickel oxide nanoparticles organized in film form by dead fungal biomass bring us closer to sustainable strategies for the biosynthesis of metal oxide nanoparticles. PMID:25228324

  14. Nickel oxide nanoparticles film produced by dead biomass of filamentous fungus

    NASA Astrophysics Data System (ADS)

    Salvadori, Marcia Regina; Nascimento, Cláudio Augusto Oller; Corrêa, Benedito

    2014-09-01

    The synthesis of nickel oxide nanoparticles in film form using dead biomass of the filamentous fungus Aspergillus aculeatus as reducing agent represents an environmentally friendly nanotechnological innovation. The optimal conditions and the capacity of dead biomass to uptake and produce nanoparticles were evaluated by analyzing the biosorption of nickel by the fungus. The structural characteristics of the film-forming nickel oxide nanoparticles were analyzed by scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), X-ray photoelectron spectroscopy (XPS), transmission electron microscopy (TEM), and atomic force microscopy (AFM). These techniques showed that the nickel oxide nanoparticles had a size of about 5.89 nm and were involved in a protein matrix which probably permitted their organization in film form. The production and uptake of nickel oxide nanoparticles organized in film form by dead fungal biomass bring us closer to sustainable strategies for the biosynthesis of metal oxide nanoparticles.

  15. Synthesis, characterization, and electrochemical properties of ordered mesoporous carbons containing nickel oxide nanoparticles using sucrose and nickel acetate in a silica template

    SciTech Connect

    Cao Yulin; Cao Jieming Zheng Mingbo; Liu Jinsong; Ji Guangbin

    2007-02-15

    New ordered mesoporous carbons containing nickel oxide nanoparticles have been successfully synthesized by carbonization of sucrose in the presence of nickel acetate inside SBA-15 mesoporous silica template. The obtained samples were characterized by X-ray diffraction (XRD), nitrogen adsorption-desorption, and transmission electron microscopy (TEM). The NiO nanoparticles were embedded inside the mesoporous carbon framework due to the simultaneous pyrolysis of nickel acetate during carbonization. The electrochemical testing of the as-made nanocomposites showed a large specific capacitance of 230 F g{sup -1} using 2 M KOH as the electrolyte at room temperature. This is attributed to the nanometer-sized NiO formed inside mesoporous carbons and the high surface area of the mesopores in which the NiO nanoparticles are formed. Furthermore, the synthetic process is proposed as a simple and general method for the preparation of new functionalized mesoporous carbon materials, for various applications in catalysis, sensor or advanced electrode material. - Graphical abstract: Schematic drawings of synthesis routes for the NiOCMK materials.

  16. Chemical weathering of layered Ni-rich oxide electrode materials: Evidence for cation exchange

    DOE PAGES

    Shkrob, Ilya A.; Gilbert, James A.; Phillips, Patrick J.; ...

    2017-05-13

    Lithiated ternary oxides containing nickel, cobalt, and manganese are intercalation compounds that are used as positive electrodes in high-energy lithium-ion batteries. These materials undergo compositional changes that adversely affect their cycling performance when they are stored in humid air or exposed to moisture. There is a new urgency to better understanding of these “weathering” processes as manufacturing moves towards a more environmentally benign aqueous processing of the positive electrode. Delithiation in the oxide subsurface regions and the formation of lithium salts (such as hydroxides and carbonates) coating the surface, have been suggested as chemical drivers for these processes, but themore » mechanistic details remain poorly known. The redox reactions which follow oxide delithiation are believed to cause all of the observed transformations. In this article we suggest another possibility: namely, the proton – lithium exchange. We argue that this hypothesis provides a simple, comprehensive rationale for our observations from X-ray diffraction, X-ray photoelectron spectroscopy, scanning transmission electron microscopy, and electrochemical measurements. These observations include contraction of the c-axis (unit cell) lattice parameter, strain in the crystalline oxide bulk, directionality of the chemical damage, formation of amorphous surface films, and the partial recovery of capacity loss by electrochemical relithiation of the material. Lastly, these effects need to be mitigated before aqueous processing of the positive electrode can find widespread adoption during cell manufacturing.« less

  17. The structure of nickel and indium oxide thin films from EXAFS data

    NASA Astrophysics Data System (ADS)

    Bets, V.; Zamozdiks, T.; Lusis, A.; Purans, J.; Bausk, N.; Sheromov, M.

    1987-11-01

    The structure of nickel oxide and indium oxide doped by tin films prepared by reactive magnetron sputtering has been studied by the EXAFS method. It has been found that the nickel oxide thin film has a microcrystalline structure with significant disorder proved by the increase of the Debye-Waller factor and the sharp decrease of peak amplitudes. The indium oxide thin film has a noticeable structural disorder due to 8% tin dopping.

  18. 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.

  19. Enhanced low-temperature power density of solid oxide fuel cell by nickel nanoparticle infiltration into pre-fired Ni/yttria-stabilized zirconia anode.

    PubMed

    Kang, Lee-Seung; Park, Jae Layng; Lee, Sungkyu; Jin, Yun-Ho; Hong, Hyun-Seon; Lee, Chan-Gi; Kim, Bum Sung

    2014-12-01

    The Ni/yttria-stabilized zirconia (YSZ) anode morphology of an anode-supported solid oxide fuel cell (SOFC) unit cell was improved by nickel nanoparticle infiltration. A colloidal route was selected for efficient fabrication of nickel metal nanoparticles and subsequent infiltration into the Ni/YSZ anode of a pre-fired SOFC unit cell. The power density of the anode-supported SOFC unit cell was measured by the potentiostatic method to investigate the effect of nickel nanoparticle infiltration. The increase in the power density of the Ni/YSZ anode with nickel nanoparticle infiltration became gradually less significant as the SOFC operating temperature increased from 700 to 800 degrees C. The improved performance of the Ni/YSZ anode with nickel nanoparticle infiltration compared to that of an anode without nickel nanoparticles is tentatively attributed to two factors: The discretely distributed nanoparticles on the nanostructured electrodes exhibited significant catalytic effects on the electrochemical performance of the electrodes, in addition to substantially increasing the triple phase boundary lengths.

  20. Performance Assessment of Single Electrode-Supported Solid Oxide Cells Operating in the Steam Electrolysis Mode

    SciTech Connect

    X. Zhang; J. E. O'Brien; R. C. O'Brien; N. Petigny

    2011-11-01

    An experimental study is under way to assess the performance of electrode-supported solid-oxide cells operating in the steam electrolysis mode for hydrogen production. Results presented in this paper were obtained from single cells, with an active area of 16 cm{sup 2} per cell. The electrolysis cells are electrode-supported, with yttria-stabilized zirconia (YSZ) electrolytes ({approx}10 {mu}m thick), nickel-YSZ steam/hydrogen electrodes ({approx}1400 {mu}m thick), and modified LSM or LSCF air-side electrodes ({approx}90 {mu}m thick). The purpose of the present study is to document and compare the performance and degradation rates of these cells in the fuel cell mode and in the electrolysis mode under various operating conditions. Initial performance was documented through a series of voltage-current (VI) sweeps and AC impedance spectroscopy measurements. Degradation was determined through long-term testing, first in the fuel cell mode, then in the electrolysis mode. Results generally indicate accelerated degradation rates in the electrolysis mode compared to the fuel cell mode, possibly due to electrode delamination. The paper also includes details of an improved single-cell test apparatus developed specifically for these experiments.

  1. Effects of the electrode oxidizing potential on underwater wet welds

    SciTech Connect

    Pope, A.M.; Liu, S.; Olson, D.L.

    1994-12-31

    Depth greatly affects the chemical composition and mechanical properties of underwater wet (UWW) welds. It is well documented in the literature that as depth increases, the amount of oxygen in the weld increases while the deoxidants decrease in concentration. To understand the influence of oxygen on the characteristics and properties of UWW welds, deposits of electrodes with different oxidizing potentials were studied. The oxidizing potentials of these electrodes were varied through additions of hematite (Fe{sub 2}O{sub 3}) to the covering of a ruffle electrode. No metallic deoxidants were used in the coverings, but MgO was added to one of the oxidizing electrodes as a possible way to control oxygen. The welds were made at 0.5 m of water depth. Chemical analysis showed that increasing oxidizing potential of the electrodes increased the weld metal oxygen content eventually reaching a plateau value of approximately 2,100 ppm. This concentration plateau is determined by the solubility limit of FeO in the liquid iron at the solidification temperature. The MgO addition was sufficient to reduce the oxygen level to 1,700 ppm. The results also showed that the effects of increasing oxidizing potential of the electrode covering on weld metal composition and microstructure are similar to those of increasing water depth. This finding is very significant since it allows for the simulation of deep water weld metal microstructures in shallow waters by controlling the oxidizing potential of the consumables used. Finally, studying the properties of oxidizing electrodes in shallow depths will also be useful in developing welding electrodes for deep waters.

  2. Carbon deposition behaviour in metal-infiltrated gadolinia doped ceria electrodes for simulated biogas upgrading in solid oxide electrolysis cells

    NASA Astrophysics Data System (ADS)

    Duboviks, V.; Lomberg, M.; Maher, R. C.; Cohen, L. F.; Brandon, N. P.; Offer, G. J.

    2015-10-01

    One of the attractive applications for reversible Solid Oxide Cells (SOCs) is to convert CO2 into CO via high temperature electrolysis, which is particularly important for biogas upgrading. To improve biogas utility, the CO2 component can be converted into fuel via electrolysis. A significant issue for SOC operation on biogas is carbon-induced catalyst deactivation. Nickel is widely used in SOC electrodes for reasons of cost and performance, but it has a low tolerance to carbon deposition. Two different modes of carbon formation on Ni-based electrodes are proposed in the present work based on ex-situ Raman measurements which are in agreement with previous studies. While copper is known to be resistant towards carbon formation, two significant issues have prevented its application in SOC electrodes - namely its relatively low melting temperature, inhibiting high temperature sintering, and low catalytic activity for hydrogen oxidation. In this study, the electrodes were prepared through a low temperature metal infiltration technique. Since the metal infiltration technique avoids high sintering temperatures, Cu-Ce0.9Gd0.1O2-δ (Cu-CGO) electrodes were fabricated and tested as an alternative to Ni-CGO electrodes. We demonstrate that the performance of Cu-CGO electrodes is equivalent to Ni-CGO electrodes, whilst carbon formation is fully suppressed when operated on biogas mixture.

  3. Electrode-nanoparticle collisions: The measurement of the sticking coefficients of gold and nickel nanoparticles from aqueous solution onto a carbon electrode

    NASA Astrophysics Data System (ADS)

    Zhou, Yi-Ge; Stuart, Emma J. E.; Pillay, Jeseelan; Vilakazi, Sibulelo; Tshikhudo, Robert; Rees, Neil V.; Compton, Richard G.

    2012-11-01

    We present experimental results to determine the proportion of nanoparticle (NP) impacts that result in adsorbed NPs, using gold and nickel nanoparticles (AuNPs/NiNPs) in collision with a glassy carbon electrode. Results are given for NP radii of 10 nm (Au) and 26 nm (Ni), as well as a range of electrode potentials. No significant systematic trends were found in either case, and the sticking coefficients were found to be s = 0.19 ± 0.03 for Au and s < 0.01 for Ni.

  4. Thermogravimetric study of the reduction of oxides of nickel and chromium

    NASA Technical Reports Server (NTRS)

    Herbell, T. P.

    1973-01-01

    The controlled hydrogen, carbon, and hydrogen-carbon reductions of the oxides of nickel and chromium were evaluated by thermogravimetric means. The materials studied were nickel (nickelous) oxide (NiO) and chromic sesquioxide (Cr2O3), mixed NiO-Cr2O3, and oxidized nickel - 20-percent chromium (Ni-20Cr). NiO was effectively reduced by all three atmospheres, Cr2O3 only by hydrogen-carbon, NiO-Cr2O3 by hydrogen and hydrogen-carbon, and oxidized Ni-20Cr by hydrogen and hydrogen-carbon and to a considerable extent by carbon alone. The results suggest that the presence of nickel promotes the reduction of Cr2O3. However, no definite explanation could be reached for the effectiveness of the hydrogen-carbon reduction of Cr2O3.

  5. Highly effective nickel sulfide counter electrode catalyst prepared by optimal hydrothermal treatment for quantum dot-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Gopi, Chandu V. V. M.; Srinivasa Rao, S.; Kim, Soo-Kyoung; Punnoose, Dinah; Kim, Hee-Je

    2015-02-01

    Nickel sulfide (NiS) thin film has been deposited on a fluorine-doped tin oxide substrate by a hydrothermal method using 3-mercaptopropionic acid and used as an efficient counter electrode (CE) for polysulfide redox reactions in quantum dot-sensitized solar cells (QDSSCs). NiS has low toxicity and environmental compatibility. In the present study, the size of the NiS nanoparticle increases with the hydrothermal deposition time. The performance of the QDSSCs is examined in detail using polysulfide electrolyte with the NiS CE. A TiO2/CdS/CdSe/ZnS-based QDSSC using the NiS CE shows enhanced photovoltaic performance with a power conversion efficiency (PCE) of 3.03%, which is superior to that of a cell with Pt CE (PCE 2.20%) under one sun illumination (AM 1.5, 100 mW cm-2). The improved photovoltaic performance of the NiS-based QDSSC may be attributed to a low charge transfer resistance (5.08 Ω) for the reduction of polysulfide on the CE, indicating greater electrocatalytic activity of the NiS. Electrochemical impedance spectroscopy, cyclic voltammetry, and Tafel-polarization measurements were used to investigate the electrocatalytic activity of the NiS and Pt CEs.

  6. Scalable Preparation of Ternary Hierarchical Silicon Oxide-Nickel-Graphite Composites for Lithium-Ion Batteries.

    PubMed

    Wang, Jing; Bao, Wurigumula; Ma, Lu; Tan, Guoqiang; Su, Yuefeng; Chen, Shi; Wu, Feng; Lu, Jun; Amine, Khalil

    2015-12-07

    Silicon monoxide is a promising anode candidate because of its high theoretical capacity and good cycle performance. To solve the problems associated with this material, including large volume changes during charge-discharge processes, we report a ternary hierarchical silicon oxide-nickel-graphite composite prepared by a facile two-step ball-milling method. The composite consists of nano-Si dispersed silicon oxides embedded in nano-Ni/graphite matrices (Si@SiOx /Ni/graphite). In the composite, crystalline nano-Si particles are generated by the mechanochemical reduction of SiO by ball milling with Ni. These nano-Si dispersed oxides have abundant electrochemical activity and can provide high Li-ion storage capacity. Furthermore, the milled nano-Ni/graphite matrices stick well to active materials and interconnect to form a crosslinked framework, which functions as an electrical highway and a mechanical backbone so that all silicon oxide particles become electrochemically active. Owing to these advanced structural and electrochemical characteristics, the composite enhances the utilization efficiency of SiO, accommodates its large volume expansion upon cycling, and has good ionic and electronic conductivity. The composite electrodes thus exhibit substantial improvements in electrochemical performance. This ternary hierarchical Si@SiOx /Ni/graphite composite is a promising candidate anode material for high-energy lithium-ion batteries. Additionally, the mechanochemical ball-milling method is low cost and easy to reproduce, indicating potential for the commercial production of the composite materials.

  7. Hole doping in Al-containing nickel oxide materials to improve electrochromic performance.

    PubMed

    Lin, Feng; Nordlund, Dennis; Weng, Tsu-Chien; Moore, Rob G; Gillaspie, Dane T; Dillon, Anne C; Richards, Ryan M; Engtrakul, Chaiwat

    2013-01-23

    Electrochromic materials exhibit switchable optical properties that can find applications in various fields, including smart windows, nonemissive displays, and semiconductors. High-performing nickel oxide electrochromic materials have been realized by controlling the material composition and tuning the nanostructural morphology. Post-treatment techniques could represent efficient and cost-effective approaches for performance enhancement. Herein, we report on a post-processing ozone technique that improves the electrochromic performance of an aluminum-containing nickel oxide material in lithium-ion electrolytes. The resulting materials were studied using X-ray diffraction (XRD), scanning electron microscopy (SEM), X-ray photoelectron spectroscopy (XPS), ultraviolet-visible-near-infrared (UV-vis-NIR) spectroscopy, and X-ray absorption spectroscopy (XAS). It was observed that ozone exposure increased the Ni oxidation state by introducing hole states in the NiO(6) octahedral unit. In addition, ozone exposure gives rise to higher-performing aluminum-containing nickel oxide films, relative to nickel oxide containing both Al and Li, in terms of switching kinetics, bleached-state transparency, and optical modulation. The improved performance is attributed to the decreased crystallinity and increased nickel oxidation state in aluminum-containing nickel oxide electrochromic films. The present study provides an alternative route to improve electrochromic performance for nickel oxide materials.

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

    DOE PAGES

    Hatzell, Kelsey B.; Hatzell, Marta C.; Cook, Kevin M.; ...

    2015-01-29

    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. We examine chemical oxidation of granular activated carbon (AC) 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)more » 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 %. Finally, 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.« less

  9. 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

    2015-03-03

    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.

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

    SciTech Connect

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

    2015-01-29

    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. We examine chemical oxidation of granular activated carbon (AC) 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 %. Finally, 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.

  11. Mortality among welders, including a group exposed to nickel oxides

    SciTech Connect

    Polednak, A.P.

    1981-09-01

    Mortality and causes of death were examined among 1059 white male welders employed between 1943 and 1973 at three plants in Oak Ridge, Tennessee. Based on deaths reported as of 1974, the standardized mortality ratio (SMR) for all causes was 87 (173 deaths observed vs. 199.0 expected on the basis of death rates for US white males). There were no deaths resulting from sinonasal cancer, and the SMR for lung cancer was 150 (95% confidence limits = 87 and 240). A subgroup of these welders (N = 536) was exposed to nickel oxides at the Oak Ridge Gaseous Diffusion (K-25) Plant; recent air concentrations of nickel (from personal air samplers) were greater than proposed standards. Standardized mortality ratios for lung cancer and diseases of the respiratory system were not higher among K-25 Plant welders than among other welders (N = 523). Welders employed for less than or equal to 50 wk at the K-25 Plant had an SMR for lung cancer of 188 (95% confidence limits = 61 and 438) based on small numbers of deaths (5 observed vs. 2.66 expected). Further follow-up of these groups is needed.

  12. rf plasma oxidation of Ni thin films sputter deposited to generate thin nickel oxide layers

    SciTech Connect

    Hoey, Megan L.; Carlson, J. B.; Osgood, R. M. III; Kimball, B.; Buchwald, W.

    2010-10-11

    Nickel oxide (NiO) layers were formed on silicon (Si) substrates by plasma oxidation of nickel (Ni) film lines. This ultrathin NiO layer acted as a barrier layer to conduction, and was an integral part of a metal-insulator-metal (MIM) diode, completed by depositing gold (Au) on top of the oxide. The electrical and structural properties of the NiO thin film were examined using resistivity calculations, current-voltage (I-V) measurements and cross-sectional transmission electron microscopy (XTEM) imaging. The flow rate of the oxygen gas, chamber pressure, power, and exposure time and their influence on the characteristics of the NiO thin film were studied.

  13. Electrocatalytic activity of nickel oxide nanoparticles as mediatorless system for NADH and ethanol sensing at physiological pH solution.

    PubMed

    Sharifi, Ensiyeh; Salimi, Abdollah; Shams, Esmaeil

    2013-07-15

    The glassy carbon (GC) electrode modified by nickel oxide nanoparticles (NiOxNPs) is proposed as a novel electrocatalytic system for the oxidation of NADH without using any electron transfer mediator. Here, chronoamperometry was used not only as a simple method for the deposition of NiOxNPs onto the GC electrode but also as an efficient tool in the controlling of nanoparticles size and efficient electrocatalytic activity. The surface morphology and electrochemical properties of the NiOxNPs/GC electrode was investigated using scanning electron microscopy and cyclic voltammetry techniques, respectively. The NPs are deposited uniformly across the GC surface and the size of NiOxNPs varies from 20 to less than 100 nm. The NiOxNPs/GC electrode shows excellent electrocatalytic activity toward oxidation of NADH at reduced overvoltage. The detection limit and sensitivity of the modified electrode toward NADH were estimated to be 106 nM (S/N=3) and 0.052 μAμM(-1), respectively at a concentration range up to 1mM. Due to the biocompatibility of NiOxNPs toward biomolecules, this modified electrode can be used as an efficient transducer in the design of an ethanol biosensor based on the coupled alcohol dehydrogenase enzyme(ADH). Hydrodynamic amperometric detection of ethanol on the ADH-Nafion/NiOxNPs/GC modified electrode gives linear responses over the concentration range of 0.2-6mM with a detection limit of 6.4 μM and sensitivity of 36 nA mM(-1). Applicability of the proposed biosensor for ethanol detection in real samples, easy and simple preparation, being mediator free, high sensitivity and biocompatibility are the major advantages of the proposed biosensor. Copyright © 2013 Elsevier B.V. All rights reserved.

  14. Batch fabrication of mesoporous boron-doped nickel oxide nanoflowers for electrochemical capacitors

    SciTech Connect

    Yang, Jing-He; Yu, Qingtao; Li, Yamin; Mao, Liqun; Ma, Ding

    2014-11-15

    Highlights: • A new facile liquid-phase method has been employed for synthesis boron-doped NiO nanoflowers. • The specific surface area of NiO is as high as 200 m{sup 2} g{sup −1}. • NiO nanoflowers exhibit a high specific capacitance of ∼1309 F g{sup −1} at a charge and discharge current density of 3 A g{sup −1}. • NiO nanoflowers have excellent cycling ability and even after 2500 cycles there is no significant reduction in specific capacitance. - Abstract: Boron-doped nickel oxide (B-NiO) nanoflowers are prepared by simple thermal decomposition of nickel hydroxide. B-NiO is porous sphere with a diameter of about 400 nm. B-NiO nanoflowers are composed of approximately 30 nm nanoplates and the thickness of the nanosheets is approximately 3 nm. The specific surface area of the material is as high as 200 m{sup 2} g{sup −1} and the pore size distribution curves of B-NiO has three typical peaks in the range of mesoporous (5 nm, 13 nm and 18 nm). As an electrode for supercapacitors, the crystalline B-NiO nanoflowers have favorable characteristics, for instance, a specific capacitance of 1309 F g{sup −1} at a current density of 3 A g{sup −1} and no significant reduction in Coulombic efficiency after 2500 cycles at 37.5 A g{sup −1}. This remarkable electrochemical performance will make B-NiO nanoflowers a promising electrode material for high performance supercapacitors.

  15. High dielectric constant nickel-doped titanium oxide films prepared by liquid-phase deposition

    NASA Astrophysics Data System (ADS)

    Lee, Ming-Kwei; Yen, Chih-Feng; Fan, Cho-Han

    2014-09-01

    The electrical characteristics of nickel-doped titanium oxide films prepared by liquid-phase deposition on p-type (100) silicon substrate were investigated. The aqueous solutions of ammonium hexafluorotitanate and boric acid were used as precursors for the growth of titanium oxide films and the dielectric constant is 29. The dielectric constant can be improved to 94 by nickel doping at the thermal annealing at 700 °C in nitrous oxide.

  16. Terahertz-Driven Nonlinear Spin Response of Antiferromagnetic Nickel Oxide

    NASA Astrophysics Data System (ADS)

    Baierl, S.; Mentink, J. H.; Hohenleutner, M.; Braun, L.; Do, T.-M.; Lange, C.; Sell, A.; Fiebig, M.; Woltersdorf, G.; Kampfrath, T.; Huber, R.

    2016-11-01

    Terahertz magnetic fields with amplitudes of up to 0.4 Tesla drive magnon resonances in nickel oxide while the induced dynamics is recorded by femtosecond magneto-optical probing. We observe distinct spin-mediated optical nonlinearities, including oscillations at the second harmonic of the 1 THz magnon mode. The latter originate from coherent dynamics of the longitudinal component of the antiferromagnetic order parameter, which are probed by magneto-optical effects of second order in the spin deflection. These observations allow us to dynamically disentangle electronic from lattice-related contributions to magnetic linear birefringence and dichroism—information so far only accessible by ultrafast THz spin control. The nonlinearities discussed here foreshadow physics that will become essential in future subcycle spin switching.

  17. Studies on nickel-tungsten oxide thin films

    SciTech Connect

    Usha, K. S.; Sivakumar, R.; Sanjeeviraja, C.

    2014-10-15

    Nickel-Tungsten oxide (95:5) thin films were prepared by rf sputtering at 200W rf power with various substrate temperatures. X-ray diffraction study reveals the amorphous nature of films. The substrate temperature induced decrease in energy band gap with a maximum transmittance of 71%1 was observed. The Micro-Raman study shows broad peaks at 560 cm{sup −1} and 1100 cm{sup −1} correspond to Ni-O vibration and the peak at 860 cm{sup −1} can be assigned to the vibration of W-O-W bond. Photoluminescence spectra show two peaks centered on 420 nm and 485 nm corresponding to the band edge emission and vacancies created due to the addition of tungsten, respectively.

  18. Improved thermal oxidation stability of solution-processable silver nanowire transparent electrode by reduced graphene oxide.

    PubMed

    Ahn, Yumi; Jeong, Youngjun; Lee, Youngu

    2012-12-01

    Solution-processable silver nanowire-reduced graphene oxide (AgNW-rGO) hybrid transparent electrode was prepared in order to replace conventional ITO transparent electrode. AgNW-rGO hybrid transparent electrode exhibited high optical transmittance and low sheet resistance, which is comparable to ITO transparent electrode. In addition, it was found that AgNW-rGO hybrid transparent electrode exhibited highly enhanced thermal oxidation and chemical stabilities due to excellent gas-barrier property of rGO passivation layer onto AgNW film. Furthermore, the organic solar cells with AgNW-rGO hybrid transparent electrode showed good photovoltaic behavior as much as solar cells with AgNW transparent electrode. It is expected that AgNW-rGO hybrid transparent electrode can be used as a key component in various optoelectronic application such as display panels, touch screen panels, and solar cells.

  19. Hierarchical chestnut-like MnCo2O4 nanoneedles grown on nickel foam as binder-free electrode for high energy density asymmetric supercapacitors

    NASA Astrophysics Data System (ADS)

    Hui, Kwun Nam; Hui, Kwan San; Tang, Zikang; Jadhav, V. V.; Xia, Qi Xun

    2016-10-01

    Hierarchical chestnut-like manganese cobalt oxide (MnCo2O4) nanoneedles (NNs) are successfully grown on nickel foam using a facile and cost-effective hydrothermal method. High resolution TEM image further verifies that the chestnut-like MnCo2O4 structure is assembled by numerous 1D MnCo2O4 nanoneedles, which are formed by numerous interconnected MnCo2O4 nanoparticles with grain diameter of ∼10 nm. The MnCo2O4 electrode exhibits high specific capacitance of 1535 F g-1 at 1 A g-1 and good rate capability (950 F g-1 at 10 A g-1) in a 6 M KOH electrolyte. An asymmetric supercapacitor is fabricated using MnCo2O4 NNs on Ni foam (MnCo2O4 NNs/NF) as the positive electrode and graphene/NF as the negative electrode. The device shows an operation voltage of 1.5 V and delivers a high energy density of ∼60.4 Wh kg-1 at a power density of ∼375 W kg-1. Moreover, the device exhibits an excellent cycling stability of 94.3% capacitance retention after 12000 cycles at 30 A g-1. This work demonstrates that hierarchical chestnut-like MnCo2O4 NNs could be a promising electrode for the high performance energy storage devices.

  20. Flower-like nickel cobalt sulfide microspheres modified with nickel sulfide as Pt-free counter electrode for dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Huo, Jinghao; Wu, Jihuai; Zheng, Min; Tu, Yongguang; Lan, Zhang

    2016-02-01

    The nickel cobalt sulfide/nickel sulfide (NiCo2S4/NiS) microspheres which exhibit flower-like morphologies are synthesized by a two-step hydrothermal method. Then the NiCo2S4/NiS microspheres are deposited on a fluorine doped SnO2 substrate by spin-casting the isopropyl alcohol solution of as-prepared microspheres. The cyclic voltammetry, electrochemical impedance spectroscopy and Tafel tests are employed to measure the electrochemical performance of NiCo2S4/NiS counter electrode. The NiCo2S4 and NiS all are used to improve the conductivity and electrocatalytic ability of the films, and the NiS can also increase the specific surface area of microspheres. The dye-sensitized solar cells (DSSCs) with the NiCo2S4/NiS counter electrode exhibite a power conversion efficiency of 8.8%, which is higher than that of DSSC with Pt counter electrode (8.1%) under the light intensity of 100 mW cm-2 (AM 1.5 G).

  1. High gas velocity oxidation and hot corrosion testing of oxide dispersion-strengthened nickel-base alloys

    NASA Technical Reports Server (NTRS)

    Deadmore, D. L.; Lowell, C. E.

    1975-01-01

    Several oxide dispersion strengthened (ODS) nickel-base alloys were tested in high velocity gases for cyclic oxidation resistance at temperatures to 1200 C and times to 500 hours and for hot corrosion resistance at 900 C for 200 hours. Nickel-chromium-aluminum ODS alloys were found to have superior resistance to oxidation and hot corrosion when compared to bare and coated nickel-chromium ODS alloys. The best of the alloys tested had compositions of nickel - 15.5 to 16 weight percent chromium with aluminum weight percents between 4.5 and 5.0. All of the nickel-chromium-aluminum ODS materials experienced small weight losses (less than 16 mg/sq cm).

  2. Mechanism for reversible CO/CO2 electrochemical conversion on a patterned nickel electrode

    NASA Astrophysics Data System (ADS)

    Luo, Yu; Li, Wenying; Shi, Yixiang; Cai, Ningsheng

    2017-10-01

    The patterned Ni negative electrode on single-crystal YSZ in CO-CO2 atmosphere is investigated in both the solid oxide fuel cell (SOFC) and solid oxide electrolysis cell (SOEC) modes. The effects of the temperature T, partial pressure of CO and CO2 (pCO and pCO2) on the electrochemical performance are measured to obtain the intrinsic kinetic parameters by natural logarithm linear fitting. The strong dependency of surface diffusion resistance on pCO implies that surface diffusion could be related to CO(Ni). The electrochemical performance had an obviously positive correlation with T and pCO. The limitation of CO2 adsorption leads to a weak dependency of polarization on pCO2. The electrochemical performance of SOEC mode in the atmosphere without CO is 1.21 times higher than that in the atmosphere without CO2, which implies that CO electrochemical reduction could be more significant than CO2 electrochemical reduction in the patterned Ni electrode. An analytical calculation is performed for the speculation of rate-limiting steps. In the SOFC mode, CO oxidation into CO2 is speculated to be rate-determining, besides, adsorbed carbon oxidation into CO could be also non-ignorable. In the SOEC mode, CO reduction into carbon could be more probably the major electrochemical reaction on the pure Ni surface.

  3. Nickel hydroxide-carbon nanotube nanocomposites as supercapacitor electrodes: crystallinity dependent performances

    NASA Astrophysics Data System (ADS)

    Jiang, Wenchao; Zhai, Shengli; Wei, Li; Yuan, Yang; Yu, Dingshan; Wang, Liang; Wei, Jun; Chen, Yuan

    2015-08-01

    Nickel hydroxide (Ni(OH)2) is a promising pseudocapacitive material to increase the energy storage capacity of supercapacitors. Ni(OH)2 has three common crystalline structures: amorphous (amor-), α-, and β-Ni(OH)2. There is a lack of good understanding on their pros and cons as supercapacitor electrodes. In this work, we synthesized three nanocomposites with thin layers (10-15 nm) of amor-, α-, and β-Ni(OH)2 deposited on conductive multi-walled carbon nanotubes (MWCNTs). The mass loading of Ni(OH)2 is analogous in these nanocomposites, ranging from 49.1-52.2 wt% with a comparable narrow-pore size distribution centered around 4-5 nm. They were fabricated into supercapacitor electrodes at a mass loading of 6 mg cm-2 with a thickness of ˜250 μm, similar to the electrodes used in commercial supercapacitors. Our results show that MWCNT/amor-Ni(OH)2 has the highest specific capacitance (1495 or 2984 F g-1, based on the mass of total active materials or Ni(OH)2 only at the scan rate of 5 mV s-1 in 1 M KOH electrolyte). It also has the best rate capability among the three nanocomposites. Better performances can be attributed to its disordered structure, which increases its effective surface area and reduces diffusion resistance for redox reactions. However, superior performances gradually deteriorate to the same level as that of MWCNT/β-Ni(OH)2 over 3000 charge/discharge cycles, because amor- and α-Ni(OH)2 transform slowly to more ordered β-Ni(OH)2. Our results highlight that the electrochemical performances of MWCNT/Ni(OH)2 nanocomposites depend on the crystallinity of Ni(OH)2, and the performances of electrodes change upon the crystalline structure transformation of Ni(OH)2 under repeated redox reactions. Future research should focus on improving the structure stability of amor-Ni(OH)2.

  4. Preparation and characterization of chemically deposited nickel sulphide film and its application as a potential counter electrode

    NASA Astrophysics Data System (ADS)

    Ray, Jaymin; Patel, Mitesh; Ghediya, Prashant; Chaudhuri, Tapas K.

    2016-07-01

    Nickel sulphide (NiS) film has emerged as a counter electrode in many applications, such as thin film batteries, dye sensitized solar cells, and supercapacitors. In this regard, we report the direct liquid coating of pure hexagonal NiS films on glass using a precursor solution of nickel-thiourea complex. A uniform and void free film is observed using scanning electron microscopy. The room temperature electrical conductivity of ˜5 × 103 S cm-1 and the positive thermoelectric power (+6 μV K-1) specify p-type conduction. The temperature variation conductivity in the range 77-300 K depicts the transition of NiS films from conducting to semi-conducting behaviour at certain transition temperatures. Preliminary results from a cyclic voltammetry study shows the feasibility of NiS films as counter electrodes.

  5. Electrochemical behavior of heavily cycled nickel electrodes in Ni/H2 cells containing electrolytes of various KOH concentrations

    NASA Technical Reports Server (NTRS)

    Lim, H. S.; Verzwyvelt, S. A.

    1989-01-01

    A study has been made of charge and discharge voltage changes with cycling of Ni/H2 cells containing electrolytes of various KOH concentrations. A study has also been made of electrochemical behavior of the nickel electrodes from the cycled Ni/H2 cells as a function of overcharge amounts. Discharge voltages depressed gradually with cycling for cells having high KOH concentrations (31 to 36 percent), but the voltages increased for those having low KOH concentrations (21 to 26 percent). To determine if there was a crystallographic change of the active material due to cycling, electrochemical behavior of nickel electrodes was studied in an electrolyte flooded cell containing either 31 or 26 percent KOH electrolyte as a function of the amount of overcharge. The changes in discharge voltage appear to indicate crystal structure changes of active material from gamma-phase to beta-phase in low KOH concentrations, and vice versa in high KOH concentration.

  6. Chemical changes in secondary electron emission during oxidation of nickel /100/ and /111/ crystal surfaces

    NASA Technical Reports Server (NTRS)

    Holloway, P. H.; Hudson, J. B.

    1975-01-01

    Changes in the secondary electron spectra (which include chemical shifts of Auger transitions) between 0-70 eV during the oxidation of both (100) and (111) nickel surfaces are reported. The reaction sequence between oxygen and nickel is also briefly described. Emission rate changes are correlated with changes in the work function of the solid.

  7. Electrode-assisted catalytic water oxidation by a flavin derivative.

    PubMed

    Mirzakulova, Ekaterina; Khatmullin, Renat; Walpita, Janitha; Corrigan, Thomas; Vargas-Barbosa, Nella M; Vyas, Shubham; Oottikkal, Shameema; Manzer, Samuel F; Hadad, Christopher M; Glusac, Ksenija D

    2012-10-01

    The success of solar fuel technology relies on the development of efficient catalysts that can oxidize or reduce water. All molecular water-oxidation catalysts reported thus far are transition-metal complexes, however, here we report catalytic water oxidation to give oxygen by a fully organic compound, the N(5)-ethylflavinium ion, Et-Fl(+). Evolution of oxygen was detected during bulk electrolysis of aqueous Et-Fl(+) solutions at several potentials above +1.9 V versus normal hydrogen electrode. The catalysis was found to occur on glassy carbon and platinum working electrodes, but no catalysis was observed on fluoride-doped tin-oxide electrodes. Based on spectroelectrochemical results and preliminary calculations with density functional theory, one possible mechanistic route is proposed in which the oxygen evolution occurs from a peroxide intermediate formed between the oxidized flavin pseudobase and the oxidized carbon electrode. These findings offer an organic alternative to the traditional water-oxidation catalysts based on transition metals.

  8. Nickel phosphate molecular sieve as electrochemical capacitors material

    NASA Astrophysics Data System (ADS)

    Yang, Jing-He; Tan, Juan; Ma, Ding

    2014-08-01

    The nickel phosphate molecular sieve VSB-5 as an electrode material for supercapacitors is investigated by cyclic voltammetry (CV) and chronopotentiometry in alkaline media. The VSB-5 shows high specific capacitance and excellent cycling stability. The specific capacitance of VSB-5 is 2740 F g-1 at a current density of 3 A g-1 and there is no significant reduction in Coulombic efficiency after 3000 cycles at 30 A g-1. In comparison with mesoporous nickel phosphate NiPO, porous nickel hydroxide and mesoporous nickel oxide, this remarkable electrochemical performance of VSB-5 will make nickel phosphate material a promising new electrode material for high performance supercapacitors.

  9. 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.

  10. Universal electrode interface for electrocatalytic oxidation of liquid fuels.

    PubMed

    Liao, Hualing; Qiu, Zhipeng; Wan, Qijin; Wang, Zhijie; Liu, Yi; Yang, Nianjun

    2014-10-22

    Electrocatalytic oxidations of liquid fuels from alcohols, carboxylic acids, and aldehydes were realized on a universal electrode interface. Such an interface was fabricated using carbon nanotubes (CNTs) as the catalyst support and palladium nanoparticles (Pd NPs) as the electrocatalysts. The Pd NPs/CNTs nanocomposite was synthesized using the ethylene glycol reduction method. It was characterized using transmission electron microscopy, energy dispersive X-ray spectroscopy, X-ray diffraction, voltammetry, and impedance. On the Pd NPs/CNTs nanocomposite coated electrode, the oxidations of those liquid fuels occur similarly in two steps: the oxidations of freshly chemisorbed species in the forward (positive-potential) scan and then, in the reverse scan (negative-potential), the oxidations of the incompletely oxidized carbonaceous species formed during the forward scan. The oxidation charges were adopted to study their oxidation mechanisms and oxidation efficiencies. The oxidation efficiency follows the order of aldehyde (formaldehyde) > carboxylic acid (formic acid) > alcohols (ethanol > methanol > glycol > propanol). Such a Pd NPs/CNTs nanocomposite coated electrode is thus promising to be applied as the anode for the facilitation of direct fuel cells.

  11. Photovoltage response to temperature change at oxide semiconductor electrodes

    NASA Technical Reports Server (NTRS)

    Reichman, B.; Byvik, C. E.

    1981-01-01

    A study has been carried out on single crystal electrodes of TiO2, SrTiO3, and alpha-Fe2O3 and polycrystalline WO3 to investigate the effect of cell temperature on the onset potential of n-type oxide semiconductor electrodes. It is found that the change of the onset potential with temperature is due to the potential change across the Helmholtz layer. The amount of this change depends on the point of zero zeta potential (pzzp) of the semiconductor electrode. The possibility of increasing the solar-to-chemical energy conversion efficiency of a photochemical cell by increasing the cell temperature is discussed.

  12. Solar water oxidation using nickel-borate coupled BiVO4 photoelectrodes.

    PubMed

    Choi, Sung Kyu; Choi, Wonyong; Park, Hyunwoong

    2013-05-07

    A naturally abundant nickel-borate (Ni-Bi) complex is demonstrated to successfully catalyze the photoelectrochemical (PEC) water oxidation of BiVO4 electrodes at 1.23 VRHE with nearly 100% faradaic efficiency for oxygen evolution. Ni-Bi is electrodeposited (ED) and photodeposited (PD) for varying times on BiVO4 electrodes in the 0.1 M borate electrolyte with 1 mM Ni(2+) at pH 9.2. Surprisingly, optimally deposited Ni-Bi films (ED-10 s and PD-30 min) display the same layer thickness of ca. 40 nm. Both Ni-Bi films enhance the photocurrent generation of BiVO4 at 1.23 VRHE by a factor of 3-4 under AM 1.5-light irradiation (100 mW cm(-2)) along with ca. 250% increase in the incident and absorbed photon-to-current efficiencies. Impedance analysis further reveals that the charge transfer resistance at BiVO4 is markedly decreased by Ni-Bi deposits. The primary role of Ni-Bi has been suggested to be a hole-conductor making photogenerated electrons more mobile and catalyzing a four-hole transfer to water through cyclic changes between the lower and higher Ni oxidation states. However, thick Ni-Bi films (>~40 nm) significantly reduce the PEC performance of BiVO4 due to the kinetic bottleneck and charge recombination. Under identical PEC conditions (0.1 M, pH 9.2), the borate electrolyte (good proton acceptor) is found to be better than nitrate (poor proton acceptor), indicative of a proton-coupled electron transfer pathway in PEC water oxidation.

  13. Characterization of a microfluidic microbial fuel cell as a power generator based on a nickel electrode.

    PubMed

    Mardanpour, Mohammad Mahdi; Yaghmaei, Soheila

    2016-05-15

    This study reports the fabrication of a microfluidic microbial fuel cell (MFC) using nickel as a novel alternative for conventional electrodes and a non-phatogenic strain of Escherichia coli as the biocatalyst. The feasibility of a microfluidic MFC as an efficient power generator for production of bioelectricity from glucose and urea as organic substrates in human blood and urine for implantable medical devices (IMDs) was investigated. A maximum open circuit potential of 459 mV was achieved for the batch-fed microfluidic MFC. During continuous mode operation, a maximum power density of 104 Wm(-3) was obtained with nutrient broth. For the glucose-fed microfluidic MFC, the maximum power density of 5.2 μW cm(-2) obtained in this study is significantly greater than the power densities reported previously for microsized MFCs and glucose fuel cells. The maximum power density of 14 Wm(-3) obtained using urea indicates the successful performance of a microfluidic MFC using human excreta. It features high power density, self-regeneration, waste management and a low production cost (<$1), which suggest it as a promising alternative to conventional power supplies for IMDs. The performance of the microfluidic MFC as a power supply was characterized based on polarization behavior and cell potential in different substrates, operational modes, and concentrations.

  14. Nickel nanowires mesh fabricated by ion beam irradiation-induced nanoscale welding for transparent conducting electrodes

    NASA Astrophysics Data System (ADS)

    Honey, S.; Ahmad, I.; Madhuku, M.; Naseem, S.; Maaza, M.; Kennedy, J. V.

    2017-07-01

    In this report, random nickel nanowires (Ni-NWs) meshes are fabricated by ions beam irradiation-induced nanoscale welding of NWs on intersecting positions. Ni-NWs are exposed to beam of 50 KeV Argon (Ar+) ions at various fluencies in the range ~1015 ions cm-2 to 1016 ions cm-2 at room temperature. Ni-NWs are welded due to accumulation of Ar+ ions beam irradiation-induced sputtered atoms on crossing positions. Ar+ ions irradiated Ni-NWs meshes are optically transparent and optical transparency is enhanced with increase in beam fluence of Ar+ ions. Ar+ ions beam irradiation-induced welded and optically transparent mesh is then exposed to 2.75 MeV hydrogen (H+) ions at fluencies 1  ×  1015 ions cm-2, 3  ×  1015 ions cm-2 and 1  ×  1016 ions cm-2 at room temperature. MeV H+ ions irradiation-induced local heat cause melting and fusion of NWs on intersecting points and eventually lead to reduce contact resistance between Ni-NWs. Electrical conductivity is enhanced with increase in beam fluence of H+ ions. These welded highly transparent and electrically conductive Ni-NWs meshes can be employed as transparent conducting electrodes in optoelectronic devices.

  15. A transparent nickel selenide counter electrode for high efficient dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Dong, Jia; Wu, Jihuai; Jia, Jinbiao; Ge, Jinhua; Bao, Quanlin; Wang, Chaotao; Fan, Leqing

    2017-04-01

    Nickel selenide (Ni0.85Se) was synthesized by a facile one-step hydrothermal reaction and Ni0.85Se film was prepared by spin-coating Ni0.85Se ink on FTO and used as counter electrode (CE) in dye-sensitized solar cells (DSSC). The Ni0.85Se CEs not only show high transmittance in visible range, but also possess remarkable electrocatalytic activity toward I-/I3-. The electrocatalytic ability of Ni0.85Se films was verified by cyclic voltammetry, electrochemical impedance spectroscopy and Tafel polarization curves. The DSSC using Ni0.85Se CE exhibits a power conversion efficiency (PCE) of 8.96%, while the DSSC consisting of sputtered Pt CE only exhibits a PCE of 8.15%. When adding a mirror under Ni0.85Se CE, the resultant DSSC exhibits a PCE of 10.76%, which exceeds that of a DSSC based on sputtered Pt CE (8.44%) by 27.49%.

  16. Mass Transfer of Nickel-Base Alloy Covered Electrode During Shielded Metal Arc Welding

    NASA Astrophysics Data System (ADS)

    Qin, Renyao; He, Guo

    2013-03-01

    The mass transfer in shielded metal arc welding of a group of nickel-base alloy covered electrodes according to AWS specification A5.11-A5.11M was investigated by directly measuring their deposited metal compositions. The results indicate that the chromium mass-transfer coefficient is in the range of 86 to 94 pct, iron in the range of 82 to 89 pct, manganese in the range of 60 to 73 pct, niobium in the range of 44 to 56 pct, and silicon in the range of 41 to 47 pct. The metal mass-transfer coefficient from the core wire is markedly higher than that from the coating. The basicity of slag, the metal contents in the flux coating, and the welding current together affect the mass transfer. As the basicity of slag increases, the mass-transfer coefficients of Mn, Fe, and Cr slightly increase, but those of Nb and Si decrease significantly. As the niobium and manganese contents increase in the coating, their mass-transfer coefficients also increase. However, iron is different. The content of iron in the coating in the range of 8 to 20 wt pct results in the optimal effective mass transfer. The lower, or higher, iron content leads to lower mass-transfer coefficient. As the welding current increases, the mass-transfer coefficients of niobium and manganese decrease, but chromium and silicon increase. Iron has the lowest mass-transfer coefficient when welded under the operating current of 100 A.

  17. Nickel oxide hollow microsphere for non-enzyme glucose detection.

    PubMed

    Ci, Suqin; Huang, Taizhong; Wen, Zhenhai; Cui, Shumao; Mao, Shun; Steeber, Douglas A; Chen, Junhong

    2014-04-15

    A facile strategy has been developed to fabricate nickel oxide hollow microspheres (NiO-HMSs) through a solvothermal method by using a mixed solvent of ethanol and water with the assistance of sodium dodecyl sulfate (SDS). Various techniques, including transmission electron microscopy (TEM), scanning electron microscopy (SEM), and powder X-ray diffraction (XRD), were used to characterize the morphology and the structure of as-prepared samples. It was confirmed that the products possess a hollow microsphere structure that is constructed by interconnecting porous nanoplate framework. Electrochemical studies indicate that the NiO-HMS exhibits excellent stability and high catalytic activity for electrocatalytic oxidation of glucose in alkaline solutions, which enables the NiO-HMS to be used in enzyme-free amperometric sensors for glucose determination. It was demonstrated that the NiO-HMS-based glucose biosensor offers a variety of merits, such as a wide linear response window for glucose concentrations of 1.67 μM-6.87 mM, short response time (3 s), a lower detection limit of 0.53 μM (S/N=3), high sensitivity (~2.39 mA mM(-1) cm(-2)) as well as good stability and repeatability. © 2013 Published by Elsevier B.V.

  18. Periodic macroporous nanocrystalline antimony-doped tin oxide electrode.

    PubMed

    Arsenault, Eric; Soheilnia, Navid; Ozin, Geoffrey A

    2011-04-26

    Optically transparent and electrically conductive electrodes are ubiquitous in the myriad world of devices. They are an indispensable component of solar and photoelectrochemical cells, organic and polymer light emitting diodes, lasers, displays, electrochromic windows, photodetectors, and chemical sensors. The majority of the electrodes in such devices are made of large electronic band-gap doped metal oxides fashioned as a dense low-surface-area film deposited on a glass substrate. Typical transparent conducting oxide materials include indium-, fluorine-, or antimony-doped tin oxides. Herein we introduce for the first time a transparent conductive periodic macroporous electrode that has been self-assembled from 6 nm nanocrystalline antimony-doped tin oxide with high thermal stability, optimized electrical conductivity, and high quality photonic crystal properties, and present an electrochemically actuated optical light switch built from this electrode, whose operation is predicated on its unique combination of electrical, optical, and photonic properties. The ability of this macroporous electrode to host active functional materials like dyes, polymers, nanocrystals, and nanowires provides new opportunities to create devices with improved performance enabled by the large area, spatially accessible and electroactive internal surface.

  19. Nickel hydroxide nanoparticles-reduced graphene oxide nanosheets film: layer-by-layer electrochemical preparation, characterization and rifampicin sensory application.

    PubMed

    Rastgar, Shokoufeh; Shahrokhian, Saeed

    2014-02-01

    Electrochemical deposition, as a well-controlled synthesis procedure, has been used for subsequently layer-by-layer preparation of nickel hydroxide nanoparticle-reduced graphene oxide nanosheets (Ni(OH)2-RGO) on a graphene oxide (GO) film pre-cast on a glassy carbon electrode surface. The surface morphology and nature of the nano-hybrid film (Ni(OH)2-RGO) was thoroughly characterized by scanning electron and atomic force microscopy, spectroscopy and electrochemical techniques. The modified electrode appeared as an effective electro-catalytic model for analysis of rifampicin (RIF) by using linear sweep voltammetry (LSV). The prepared modified electrode exhibited a distinctly higher activity for electro-oxidation of RIF than either GO, RGO nanosheets or Ni(OH)2 nanoparticles. Enhancement of peak currents is ascribed to the fast heterogeneous electron transfer kinetics that arise from the synergistic coupling between the excellent properties of RGO nanosheets (such as high density of edge plane sites, subtle electronic characteristics and attractive π-π interaction) and unique properties of metal nanoparticles. Under the optimized analysis conditions, the modified electrode showed two oxidation processes for rifampicin at potentials about 0.08 V (peak I) and 0.69 V (peak II) in buffer solution of pH 7.0 with a wide linear dynamic range of 0.006-10.0 µmol L(-1) and 0.04-10 µmol L(-1) with a detection limit of 4.16 nmol L(-1) and 2.34 nmol L(-1) considering peaks I and II as an analytical signal, respectively. The results proved the efficacy of the fabricated modified electrode for simple, low cost and highly sensitive medicine sensor well suited for the accurate determinations of trace amounts of rifampicin in the pharmaceutical and clinical preparations.

  20. [Electrochemically reductive dechlorination of chloroform by palladium/polymeric pyrrole film/foam-nickel composite electrode in acidic system].

    PubMed

    Sun, Zhi-Rong; Ge, Hui; Hu, Xiang; Peng, Yong-Zhen

    2009-02-15

    Palladium/polymeric pyrrole film/foam-nickel (Pd/PPy/foam-Ni) composite electrode were prepared by the electrodeposition method with the electrodepositing current density of 5 mA x cm(-2) and the electrodepositing time of 40 min. Electrochemical reductive dechlorination of chloroform in acidic system was investigated using the Pd/PPy/foam-Ni electrode at ambient temperature. The electrochemical deposition behaviors of Pd/PPy/foam-Ni electrode were studied by means of cyclic voltammetry (CV). Cyclic voltammetry results reveal that the large hydrogen adsorption peak current of -100 mA on Pd/PPy/foam-Ni electrode was obtained at about -500 mV (vs Hg/Hg2 SO4). SEM micrographs show that the addition of polymeric pyrrole changed the distributing configuration of Pd microparticles on the electrode and Pd/PPy/foam-Ni electrode possessed a good spatial extension. Chloroform dechlorination experimentes were conducted in acid system. Dechlorination experimental results indicate that, with the integrated analysis of removal efficiency and current efficiency, with the high current efficiency of 44.17%, the removal efficiency of chloroform on Pd/PPy/foam-Ni electrode was 49.23%, under the optimum conditions of the dechlorination current density of 0.05 mA x cm(-2) and the dechlorination time of 180 min. In acid aqueous solution, with low initial concentration of chloroform, the results of dechlorination experiment were preferable.

  1. Electrolytic photodissociation of chemical compounds by iron oxide electrodes

    DOEpatents

    Somorjai, Gabor A.; Leygraf, Christofer H.

    1984-01-01

    Chemical compounds can be dissociated by contacting the same with a p/n type semi-conductor diode having visible light as its sole source of energy. The diode consists of low cost, readily available materials, specifically polycrystalline iron oxide doped with silicon in the case of the n-type semi-conductor electrode, and polycrystalline iron oxide doped with magnesium in the case of the p-type electrode. So long as the light source has an energy greater than 2.2 electron volts, no added energy source is needed to achieve dissociation.

  2. Electrolytic photodissociation of chemical compounds by iron oxide electrodes

    SciTech Connect

    Somorjai, G.A.; Leygraf, C.H.

    1984-07-17

    Chemical compounds can be dissociated by contacting the same with a p/n type semi-conductor diode having visible light as its sole source of energy. The diode consists of low cost, readily available materials, specifically polycrystalline iron oxide doped with silicon in the case of the n-type semi-conductor electrode, and polycrystalline iron oxide doped with magnesium in the case of the p-type electrode. So long as the light source has an energy greater than 2.2 electron volts, no added energy source is needed to achieve dissociation.

  3. Solid-electrolyte oxide-ion electrode for molten nitrates

    SciTech Connect

    Nissen, D.A.

    1981-10-01

    An oxide ion sensitive electrode of the type Pb, PbO/ZrO/sub 2/(Y/sub 2/O/sub 3/)// was constructed and its performance tested in the binary, equimolar molten salt NaNO/sub 3/-KNO/sub 3/ over the temperature range 336 to 350/sup 0/C. The response of this electrode to oxide ion concentrations over the range 10/sup -6/ to 10/sup -10/ moles/kg is linearly dependent upon log (0/sup =/), and dE/dlog(0/sup =/) corresponds to a two-electron process.

  4. Nickel

    USDA-ARS?s Scientific Manuscript database

    The agricultural significance of nickel (Ni) is becoming increasingly apparent; yet, relative few farmers, growers, specialists or researchers know much about its function in crops, nor symptoms of deficiency or toxicity. The body of knowledge is reviewed regarding Ni’s background, uptake, transloc...

  5. Oxidative stress mediated apoptosis induced by nickel ferrite nanoparticles in cultured A549 cells.

    PubMed

    Ahamed, Maqusood; Akhtar, Mohd Javed; Siddiqui, Maqsood A; Ahmad, Javed; Musarrat, Javed; Al-Khedhairy, Abdulaziz A; AlSalhi, Mohamad S; Alrokayan, Salman A

    2011-05-10

    Due to the interesting magnetic and electrical properties with good chemical and thermal stabilities, nickel ferrite nanoparticles are being utilized in many applications including magnetic resonance imaging, drug delivery and hyperthermia. Recent studies have shown that nickel ferrite nanoparticles produce cytotoxicity in mammalian cells. However, there is very limited information concerning the toxicity of nickel ferrite nanoparticles at the cellular and molecular level. The aim of this study was to investigate the cytotoxicity, oxidative stress and apoptosis induction by well-characterized nickel ferrite nanoparticles (size 26 nm) in human lung epithelial (A549) cells. Nickel ferrite nanoparticles induced dose-dependent cytotoxicity in A549 cells demonstrated by MTT, NRU and LDH assays. Nickel ferrite nanoparticles were also found to induce oxidative stress evidenced by generation of reactive oxygen species (ROS) and depletion of antioxidant glutathione (GSH). Further, co-treatment with the antioxidant L-ascorbic acid mitigated the ROS generation and GSH depletion due to nickel ferrite nanoparticles suggesting the potential mechanism of oxidative stress. Quantitative real-time PCR analysis demonstrated that following the exposure of A549 cells to nickel ferrite nanoparticles, the level of mRNA expressions of cell cycle checkpoint protein p53 and apoptotic proteins (bax, caspase-3 and caspase-9) were significantly up-regulated, whereas the expression of anti-apoptotic proteins (survivin and bcl-2) were down-regulated. Moreover, activities of caspase-3 and caspase-9 enzymes were also significantly higher in nickel ferrite nanoparticles exposed cells. To the best of our knowledge this is the first report showing that nickel ferrite nanoparticles induced apoptosis in A549 cells through ROS generation and oxidative stress via p53, survivin, bax/bcl-2 and caspase pathways.

  6. Effect of charging methods on battery electrodes

    NASA Astrophysics Data System (ADS)

    McBreen, J.

    The effect of modified charging methods on the structure and behavior of several battery electrodes are reviewed. These include the alkaline cadmium, zinc, silver oxide and nickel oxide electrodes. Also included are recent results obtained for pasted zinc electrodes and in acidic zinc chloride electrolytes. Modified charging methods can greatly affect electrodes particularly when the charging reaction involving the nucleation, and growth of a new phase. Many of the observed morphological effects are described with regard to nucleation and orientation effects.

  7. High-performance Ti/BDD electrodes for pollutant oxidation.

    PubMed

    Chen, Xueming; Chen, Guohua; Gao, Furong; Yue, Po Lock

    2003-11-01

    Deposition of stable boron-doped diamond (BDD) films on Ti substrates is believed to be very difficult. In the present study, the stability of Ti/BDD electrodes has been significantly improved by using an organic additive, CH2(OCH3)2. The improved electrodes had service lives of 175-264 h under accelerated life test conditions, which are 2.3-3.0 times longer than the service lives of electrodes prepared with the conventional H2 + CH4 mixture. Raman spectroscopy, X-ray diffraction (XRD), and scanning electron microscopy (SEM) examinations demonstrated thatthe films had well-defined diamond features. The current efficiency (CE) obtained on Ti/BDD was 46.9-78.5% in oxidizing acetic acid, maleic acid, phenol, and dyes, which is 1.6-4.3-fold higher than that obtained on the typical Ti/ Sb2O5-SnO2 electrode. We used a Ti/BDD electrode prepared with H2 + CH4 + CH2(OCH3)2 for over 300 h; its activity remained superior. The successful development of stable and active Ti/BDD electrodes significantly increases the feasibility of industrial applications of anodic oxidation in wastewater treatment.

  8. An analytical approach for solid oxide cell electrode geometric design

    NASA Astrophysics Data System (ADS)

    Nelson, George J.

    2015-12-01

    An analytical model for gas distributions in porous solid oxide cell electrodes is applied to develop dimensionless metrics that describe electrode performance. These metrics include two forms of a dimensionless reactant depletion current density and a geometry sensitive Damköhler number used to assess electrode catalytic effectiveness. The first dimensionless depletion current density defines when reducing electrode thickness no longer benefits mass transfer performance for a given cell geometry. The second dimensionless depletion current density provides a gage of deviation from the limiting current behavior predicted using button-cell experimental and modeling approaches. The Damköhler number and related catalytic effectiveness quantify two-dimensional transport effects under non-depleted operating conditions, providing a means of generalizing insights from reactant depletion behavior for typical cell operating conditions. A finite element solution for gas transport based on the dusty-gas model is used as a benchmark for the analytical model and dimensionless metrics. Estimates of concentration polarization based on analytical and numerical models compare well to published experimental data. Analytical performance predictions provide clear demonstration of the influence of two-dimensional electrode geometry on solid oxide cell performance. These results agree with finite element predictions and suggest that reduction of electrode thickness does not exclusively benefit cell performance.

  9. Impedance studies of nickel/cadmium and nickel/hydrogen cells using the cell case as a reference electrode

    NASA Technical Reports Server (NTRS)

    Reid, Margaret A.

    1990-01-01

    Impedance measurements have been made on several Ni/Cd and Ni/H2 flight-weight cells using the case as a reference electrode. For these measurements, the voltage of the case with respect to the anode or cathode is unimportant provided that it remains stable during the measurement of the impedance. In the cells measured so far, the voltage of the cell cases with respect to the individual electrodes differ from cell to cell, even at the same overall cell voltage, but they remain stable with time. The measurements can thus be used to separate the cell impedance into the contributions of each electrode, allowing improved diagnosis of cell problems.

  10. Oxidation of TD nickel at 1050 C and 1200 C as compared with three grades of nickel of different purity

    NASA Technical Reports Server (NTRS)

    Lowell, C. E.; Grisaffe, S. J.; Deadmore, D. L.

    1972-01-01

    The isothermal oxidation of three nickels of different purity, Ni-200, Ni-270, and JM-Ni, was compared with that of TD-Ni in air at 1050 and 1200 C. The samples were oxidized as ground, as polished, or as annealed and polished. Weight change, metal loss, scale thickness, oxide morphology, and scale texture were determined. In degree of oxidation, TD-Ni was nearly the same as the higher purity materials, Ni-270 and JM-Ni; and less pure Ni-200 oxidized more than the others. However, in microstructure and scale texture the TD-Ni more closely resembled Ni-200. Grinding only charged the texture of the oxides of Ni_200 and TD-Ni.

  11. Nickel(II)-induced nasal epithelial toxicity and oxidative mitochondrial damage.

    PubMed

    Lee, Yoon-Jin; Lim, Soo-Sung; Baek, Byoung Joon; An, Je-Min; Nam, Hae-Seon; Woo, Kee-Min; Cho, Moon-Kyun; Kim, Sung-Ho; Lee, Sang-Han

    2016-03-01

    In probing the underlying mechanisms of nickel(II)-induced cytotoxicity on nasal epithelium, we investigated the effects of nickel(II) acetate on nasal epithelial RPMI-2650 cells. Nickel(II) elicited apoptosis, as signified by pyknotic and fragmented nuclei, increased caspase-3/7 activity, and an increase in annexin V binding, hypodiploid DNA, and Bax/Bcl-2 protein ratio. Nickel(II)-induced G2/M arrest was associated with up-regulation of p21(WAF1/CIP1) expression, decrease in phosphorylation at Thr(161) of Cdc2, and down-regulation of cyclin B1. Associated with these responses, ROS generation and mitochondrial depolarization increased in a nickel(II) concentration-dependent fashion. Pretreatment with N-acetylcysteine (NAC) attenuated these changes. p53 reporter gene assay and analyses of p53, Puma, Bax, and Bcl-2 protein levels indicated that NAC inhibited nickel(II)-induced activation of p53-mediated mitochondrial apoptotic pathway. Collectively, our study provides evidences that nickel(II) may induce oxidative damage on nasal epithelium in which antioxidant NAC protects cells against nickel(II)-induced apoptosis through the prevention of oxidative stress-mediated mitochondrial damage.

  12. Effect of pressure on capacitor electrodes formed with oxide nanoparticles

    NASA Astrophysics Data System (ADS)

    Giaume, D.; Pétrissans, X.; Barboux, P.

    2014-12-01

    The effect of compactness and pressure on the conductivity of supercapacitor electrodes and their resulting electrochemical properties is studied. Mixtures of cobalt oxides MxCoO2 (M = H or Na) with carbon and polymer additives are studied under pressures up to 20 MPa. A power function links the compactness and the resistivity of the powder formulations in this pressure range, coherent with powder rearrangement and grain packing. Although the cobalt oxide grains have a metallic character, the powders remain quite resistive because of weak connections between the grains. Carbon additives enhance the intergranular conductivity in dry formulations and the resistivity mainly depends on the carbon volume content. Electrochemical measurements on a symmetric cell using formulated electrodes in a Na2SO4 electrolyte clearly show a large positive effect of the pressure on the electrochemical performances of the cell: After release of the pressure, the electrode retains a part of its optimum performance.

  13. Clad modified optical fiber gas sensors based on nanocrystalline nickel oxide embedded coatings

    NASA Astrophysics Data System (ADS)

    Yamini, K.; Renganathan, B.; Ganesan, A. R.; Prakash, T.

    2017-07-01

    A clad modified optical fiber gas sensor for sensing volatile organic compound vapours (VOCs) such as formaldehyde (HCHO), ammonia (NH3), ethanol (C2H5OH) and methanol (CH3OH) up to 500 ppm was studied using nanocrystalline nickel oxide embedded coatings. Prior to the measurements, nickel oxide in two different crystallite sizes such as 24 nm and 76 nm was synthesized by calcination of reverse precipitated nickel hydroxide subsequently at 450 °C and 900 °C for 30 min. Then, samples physical properties were characterized using X-ray diffraction (XRD), thermogravimetric analysis (TGA), Fourier transform infrared spectroscopy (FTIR), field emission scanning electron microscopy (FESEM) and high resolution transmission electron microscopy (HRTEM). Our gas sensing measurement concludes that the lower crystallite size (24 nm) nickel oxide nanocrystals exhibits superior performance to formaldehyde and ethanol vapours as compared with other two VOCs, the observed experimental results were discussed in detail.

  14. Chronic exposure to iron oxide, chromium oxide, and nickel oxide fumes of metal dressers in a steelworks

    PubMed Central

    Jones, J. Graham; Warner, C. G.

    1972-01-01

    Graham Jones, J., and Warner, C. G. (1972).Brit. J. industr. Med.,29, 169-177. Chronic exposure to iron oxide, chromium oxide, and nickel oxide fumes of metal dressers in a steelworks. Occupational and medical histories, smoking habits, respiratory symptoms, chest radiographs, and ventilatory capacities were studied in 14 steelworkers employed as deseamers of steel ingots for periods of up to 16 years. The men were exposed for approximately five hours of each working shift to fume concentrations ranging from 1·3 to 294·1 mg/m3 made up mainly of iron oxide with varying proportions of chromium oxide and nickel oxide. Four of the men, with 14 to 16 years' exposure, showed radiological evidence of pneumoconiosis classified as ILO categories 2 or 3. Of these, two had pulmonary function within the normal range and two had measurable loss of function, moderate in one case and mild in the other. Many observers would diagnose these cases as siderosis but the authors consider that this term should be reserved for cases exposed to pure iron compounds. The correct diagnosis is mixed-dust pneumoconiosis and the loss of pulmonary function is caused by the effects of the mixture of metallic oxides. It is probable that inhalation of pure iron oxide does not cause fibrotic pulmonary changes, whereas the inhalation of iron oxide plus certain other substances obviously does. Images PMID:5021996

  15. Molybdenum-platinum-oxide electrodes for thermoelectric generators

    DOEpatents

    Schmatz, Duane J.

    1990-01-01

    The invention is directed to a composite article suitable for use in thermoelectric generators. The article comprises a solid electrolyte carrying a thin film comprising molybdenum-platinum-oxide as an electrode deposited by physical deposition techniques. The invention is also directed to the method of making same.

  16. Stimuli-responsive electrodes detect oxidative stress and liver injury.

    PubMed

    Aran, Kiana; Parades, Jacobo; Rafi, Mohammad; Yau, Jennifer F; Acharya, Abhinav P; Zibinsky, Mikhail; Liepmann, Dorian; Murthy, Niren

    2015-02-25

    A digital point-of-care biosensor for measuring reactive oxygen species is presented based on novel reactive oxygen species responsive polymer-based electrodes. The biosensor is able to detect a drug-induced liver injury by monitoring the oxidative stress in the blood.

  17. Oxidative Dissolution of Nickel Metal in Hydrogenated Hydrothermal Solutions

    SciTech Connect

    Ziemniak, S. E.; Guilmette, P. A.; Turcotte, R. A.; Tunison, H. M.

    2007-03-27

    A platinum-lined, flowing autoclave facility is used to investigate the solubility behavior of metallic nickel in hydrogenated ammonia and sodium hydroxide solutions between 175 and 315 C. The solubility measurements were interpreted by means of an oxidative dissolution reaction followed by a sequence of Ni(II) ion hydrolysis reactions: Ni(s) + 2H+(aq) = Ni2+(aq) + H2(g) and Ni{sup 2+}(aq) + nH{sub 2}O = Ni(OH){sub n}{sup 2-n}(aq) + nH{sup +}(aq) where n = 1 and 2. Gibbs energies associated with these reaction equilibria were determined from a least-squares analysis of the data. The extracted thermochemical properties ({Delta}fG{sup 0}, {Delta}fH{sup 0} and S{sup 0}) for Ni2{sup +}(aq), Ni(OH){sup +}(aq) and Ni(OH){sub 2}(aq) were found to be consistent with those determined in a previous solubility study of NiO/Ni(OH){sub 2} conducted in our laboratory. The thermodynamic basis of the Ni/NiO phase boundary in aqueous solutions is examined to show that Ni(s) is stable relative to NiO(s) in solutions saturated at 25 C with 1 atm H{sub 2} for temperatures below 309 C.

  18. Adhesion of Germanium Electrode on Nickel Substrate for Lithium Ion Battery Applications

    NASA Astrophysics Data System (ADS)

    Jeyaranjan, Aadithya

    Lithium ion batteries (LIBs) have gained increasing popularity due to their high potential, low self-discharge, zero priming and minimal memory effect. However, the emergence of electrical vehicles and hybrid electrical vehicles in the automobile industry, where LIBs are predominantly in use, instilled a need to improve LIB batteries by experimenting with new materials. Graphite, the commonly used anode material for LIBs suffers from low theoretical capacity (372 mA h g-1) and torpid rate performance. Germanium (Ge) seems to be a promising substitute of carbon due to its high theoretical capacity, high Li+ diffusivity and electrical conductivity. However, Ge undergoes large volumetric change (+/-370%). This causes deboning of the thin film Ge electrode from the substrate current collector, causing a rapid decrease in the electrolytic performance. The process of ion beam mixing claims to have overcome this problem. In our current study, the adhesion strength of Ge thin film over Nickel (Ni) substrate (with and without ion beam mixing) is being measured using nanoindentation and the superlayer indentation test. Nanoindentation is one of the popular techniques to measure the mechanical properties and adhesion of thin film coatings. In this technique, a very small indenter of a desired geometry indents the film/substrate pair and the work of adhesion is calculated by knowing the plastic depth of indentation and the radius of indentation. Superlayer indentation is analogous to normal indentation but with a highly stressed superlayer on top to restrict the out-of-plane displacements, it reduces the plastic pile up around the indenter tip. The results from our study strongly suggest the possibility of dramatically increasing the adhesion strength by ion bombardment, which can be achieved by atomic level intermixing of the film/substrate pair. These, in turn, suggest that Ge could be an effective successor to graphite in the near future.

  19. Melting of oxidized nickel ores in a barbotage unit: II. Experimental investigations

    NASA Astrophysics Data System (ADS)

    Starykh, R. V.; Pakhomov, R. A.

    2016-07-01

    The possibility of efficient processing of oxidized nickel ores (ONOs) to form ferronickel in a barbotage unit (liquid bath melting (LBM), Vanyukov furnace) is corroborated theoretically and experimentally. The processing of the ONOs of the Buruktal deposit with the formation of ferronickel under the conditions that model melting in a barbotage unit is subjected to laboratory investigations. Wet or dried ore and its reduced cinder are melted. It is shown that melting of the reduced cinder of ONO can result in the formation of nickel-rich (up to 40% Ni) ferronickel upon the extraction of more than 91% nickel from the raw materials at a residual nickel content of <0.1% in a slag. Direct melting of the ore results in the formation of ferronickel with at most 18% Ni and a low degree of nickel extraction into ferronickel, which has high sulfur, phosphorus, and carbon contents in this case.

  20. Fragmentation of [Ni(NO3)3](-): A Study of Nickel-Oxygen Bonding and Oxidation States in Nickel Oxide Fragments.

    PubMed

    Hester, Thomas H; Albury, Rachael M; Pruitt, Carrie Jo M; Goebbert, Daniel J

    2016-07-05

    Gas-phase nickel nitrate anions are known to produce nickel oxide nitrate anions, [NiOx(NO3)y](-) upon fragmentation. The goal of this study was to investigate the properties of nickel oxide nitrate complexes generated by electrospray ionization using a tandem quadrupole mass spectrometer and theoretical calculations. The [Ni(NO3)3](-) ion undergoes sequential NO2(•) elimination to yield [NiO(NO3)2](-) and [NiO2(NO3)](-), followed by elimination of O2. The electronic structure of the nickel oxide core influences decomposition. Calculations indicate electron density from oxygen is delocalized onto the metal, yielding a partially oxidized oxygen in [NiO(NO3)2](-). Theoretical studies suggest the mechanism for O2 elimination from [NiO2(NO3)](-) involves oxygen atom transfer from a nitrate ligand to yield an intermediate, [NiO(O2)(NO2)](-), containing an oxygen radical anion ligand, O(•-), a superoxide ligand, O2(•-), and a nitrite ligand bound to Ni(2+). Electron transfer from superoxide partially reduces both the metal and oxygen and yields the energetically favored [NiO(NO2)](-) + O2 products.

  1. 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.

  2. 4 kW Test of Solid Oxide Electrolysis Stacks with Advanced Electrode-Supported Cells

    SciTech Connect

    J. E. O'Brien; X. Zhang; G. K. Housley; L. Moore-McAteer; G. Tao

    2012-06-01

    A new test stand has been developed at the Idaho National Laboratory for multi-kW testing of solid oxide electrolysis stacks. This test stand will initially be operated at the 4 KW scale. The 4 kW tests will include two 60-cell stacks operating in parallel in a single hot zone. The stacks are internally manifolded with an inverted-U flow pattern and an active area of 100 cm2 per cell. Process gases to and from the two stacks are distributed from common inlet/outlet tubing using a custom base manifold unit that also serves as the bottom current collector plate. The solid oxide cells incorporate a negative-electrode-supported multi-layer design with nickel-zirconia cermet negative electrodes, thin-film yttria-stabilized zirconia electrolytes, and multi-layer lanthanum ferrite-based positive electrodes. Treated metallic interconnects with integral flow channels separate the cells and electrode gases. Sealing is accomplished with compliant mica-glass seals. A spring-loaded test fixture is used for mechanical stack compression. Due to the power level and the large number of cells in the hot zone, process gas flow rates are high and heat recuperation is required to preheat the cold inlet gases upstream of the furnace. Heat recuperation is achieved by means of two inconel tube-in-tube counter-flow heat exchangers. A current density of 0.3 A/cm2 will be used for these tests, resulting in a hydrogen production rate of 25 NL/min. Inlet steam flow rates will be set to achieve a steam utilization value of 50%. The 4 kW test will be performed for a minimum duration of 1000 hours in order to document the long-term durability of the stacks. Details of the test apparatus and initial results will be provided.

  3. Effect of Electrode Configuration on Nitric Oxide Gas Sensor Behavior

    PubMed Central

    Cui, Ling; Murray, Erica P.

    2015-01-01

    The influence of electrode configuration on the impedancemetric response of nitric oxide (NO) gas sensors was investigated for solid electrochemical cells [Au/yttria-stabilized zirconia (YSZ)/Au)]. Fabrication of the sensors was carried out at 1050 °C in order to establish a porous YSZ electrolyte that enabled gas diffusion. Two electrode configurations were studied where Au wire electrodes were either embedded within or wrapped around the YSZ electrolyte. The electrical response of the sensors was collected via impedance spectroscopy under various operating conditions where gas concentrations ranged from 0 to 100 ppm NO and 1%–18% O2 at temperatures varying from 600 to 700 °C. Gas diffusion appeared to be a rate-limiting mechanism in sensors where the electrode configuration resulted in longer diffusion pathways. The temperature dependence of the NO sensors studied was independent of the electrode configuration. Analysis of the impedance data, along with equivalent circuit modeling indicated the electrode configuration of the sensor effected gas and ionic transport pathways, capacitance behavior, and NO sensitivity. PMID:26404312

  4. Electrodeposited iridium oxide for neural stimulation and recording electrodes.

    PubMed

    Meyer, R D; Cogan, S F; Nguyen, T H; Rauh, R D

    2001-03-01

    Iridium oxide films formed by electrodeposition onto noniridium metal substrates are compared with activated iridium oxide films (AIROFs) as a low impedance, high charge capacity coating for neural stimulation and recording electrodes. The electrodeposited iridium oxide films (EIROFs) were deposited on Au, Pt, PtIr, and 316 LVM stainless steel substrates from a solution of IrCl4, oxalic acid, and K2CO3. A deposition protocol involving 50 potential sweeps at 50 mV/s between limits of 0.0 V and 0.55 V (versus Ag AgCl) followed by potential pulsing between the same limits produced adherent films with a charge storage capacity of >25 mC/cm2. Characterization by cyclic voltammetry and impedance spectroscopy revealed no differences in the electrochemical behavior of EIROF on non-Ir substrates and AIROF. The mechanical stability of the oxides was evaluated by ultrasonication in distilled water followed by dehydration and rehydration. Stability under charge injection was evaluated using 200 micros, 5.9 A/cm2 (1.2 mC/cm2) cathodal pulses. Loss of iridium oxide charge capacity was comparable for AIROFs and the EIROFs, ranging from 1% to 8% of the capacity immediately after activation or deposition. The EIROFs were deposited and evaluated on silicon microprobe electrodes and on metallized polyimide electrodes being developed for neural recording and stimulation applications.

  5. Design of a neutral three-dimensional electro-Fenton system with foam nickel as particle electrodes for wastewater treatment.

    PubMed

    Liu, Wei; Ai, Zhihui; Zhang, Lizhi

    2012-12-01

    In this work, we demonstrate a novel three-dimensional electro-Fenton system (3D-E-Fenton) for wastewater treatment with foam nickel, activated carbon fiber and Ti/RuO(2)-IrO(2) as the particle electrodes, the cathode, and the anode respectively. This 3D-E-Fenton system could exhibit much higher rhodamine B removal efficiency (99%) than the counterpart three-dimensional electrochemical system (33%) and E-Fenton system (19%) at neutral pH in 30 min. The degradation efficiency enhancement was attributed to much more hydroxyl radicals generated in the 3D-E-Fenton system because foam nickel particle electrodes could activate molecular oxygen to produce O(2)(-) via a single-electron transfer pathway to subsequently generate more H(2)O(2) and hydroxyl radicals. This is the first observation of molecular oxygen activation over the particle electrodes in the three-dimensional electrochemical system. These interesting findings could provide some new insight on the development of high efficient E-Fenton system for wastewater treatment at neutral pH. Copyright © 2012 Elsevier B.V. All rights reserved.

  6. The Effect of Anodic Oxide Films on the Nickel-Aluminum Reaction in Aluminum Braze Sheet

    NASA Astrophysics Data System (ADS)

    Tadgell, Colin A.; Wells, Mary A.; Corbin, Stephen F.; Colley, Leo; Cheadle, Brian; Winkler, Sooky

    2017-01-01

    The influence of an anodic oxide surface film on the nickel-aluminum reaction at the surface of aluminum brazing sheet has been investigated. Samples were anodized in a barrier-type solution and subsequently sputtered with nickel. Differential scanning calorimetry (DSC) and metallography were used as the main investigative techniques. The thickness of the anodic film was found to control the reaction between the aluminum substrate and nickel coating. Solid-state formation of nickel-aluminum intermetallic phases occurred readily when a relatively thin oxide film (13 to 25 nm) was present, whereas intermetallic formation was suppressed in the presence of thicker oxides ( 60 nm). At an intermediate oxide film thickness of 35 nm, the Al3Ni phase formed shortly after the initiation of melting in the aluminum substrate. Analysis of DSC traces showed that formation of nickel-aluminum intermetallic phases changed the melting characteristics of the aluminum substrate, and that the extent of this change can be used as an indirect measure of the amount of nickel incorporated into the intermetallic phases.

  7. The Effect of Anodic Oxide Films on the Nickel-Aluminum Reaction in Aluminum Braze Sheet

    NASA Astrophysics Data System (ADS)

    Tadgell, Colin A.; Wells, Mary A.; Corbin, Stephen F.; Colley, Leo; Cheadle, Brian; Winkler, Sooky

    2017-03-01

    The influence of an anodic oxide surface film on the nickel-aluminum reaction at the surface of aluminum brazing sheet has been investigated. Samples were anodized in a barrier-type solution and subsequently sputtered with nickel. Differential scanning calorimetry (DSC) and metallography were used as the main investigative techniques. The thickness of the anodic film was found to control the reaction between the aluminum substrate and nickel coating. Solid-state formation of nickel-aluminum intermetallic phases occurred readily when a relatively thin oxide film (13 to 25 nm) was present, whereas intermetallic formation was suppressed in the presence of thicker oxides ( 60 nm). At an intermediate oxide film thickness of 35 nm, the Al3Ni phase formed shortly after the initiation of melting in the aluminum substrate. Analysis of DSC traces showed that formation of nickel-aluminum intermetallic phases changed the melting characteristics of the aluminum substrate, and that the extent of this change can be used as an indirect measure of the amount of nickel incorporated into the intermetallic phases.

  8. Sputtered iridium oxide for stimulation electrode coatings.

    PubMed

    Mokwa, Wilfried; Wessling, Boerge; Schnakenberg, Uwe

    2007-01-01

    This work deals with the reactive RF-powered sputter deposition of iridium oxide for use as the active stimulation layer in functional medical implants. The oxygen gettered by the growing films is determined by an approach based on generic curves. Films deposited at different stages of oxygen integration show strong differences in electrochemical behaviour, caused by different morphologies. The dependence of electrochemical activity on morphology is further illustrated by RF sputtering onto heated substrates, as well as DC sputtering onto cold substrates.

  9. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2006-11-14

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

  10. High temperature coefficient of resistance molybdenum oxide and nickel oxide thin films for microbolometer applications

    NASA Astrophysics Data System (ADS)

    Jin, Yao O.; John, David Saint; Podraza, Nikolas J.; Jackson, Thomas N.; Horn, Mark W.

    2015-03-01

    Molybdenum oxide (MoOx) and nickel oxide (NiOx) thin films were deposited by reactive biased target ion beam deposition. MoOx thin film resistivity varied from 3 to 2000 Ω.cm with a temperature coefficient of resistance (TCR) from -1.7% to -3.2%/K, and NiOx thin film resistivity varied from 1 to 300 Ω.cm with a TCR from -2.2% to -3.3%/K, both easily controlled by varying the oxygen partial pressure. Biased target ion beam deposited high TCR MoOx and NiOx thin films are polycrystalline semiconductors and have good stability in air. Compared with commonly used vanadium oxide thin films, MoOx or NiOx thin films offer improved process control for resistive temperature sensors.

  11. Fabrication and characterization of protonic-ceramic fuel cells and electrolysis cells utilizing infiltrated lanthanum nickelate electrodes

    NASA Astrophysics Data System (ADS)

    Babiniec, Sean M.

    High-temperature protonic ceramics (HTPCs) have gained interest as fuel cell and electrolysis cell electrolytes, as well as hydrogen separation membranes. The transport of hydrogen as opposed to oxygen results in several benefits and applications, including higher fuel efficiency, dehydrogenation of fuel streams, and hydrogen-based chemical synthesis. However, limited work has been done in the development of air/steam electrodes for these devices. This work presents the characterization of lanthanum nickelate, La 2NiO4+delta (LN), as a potential air/steam electrode material for use with BaCe0.2Zr0.7Y0.1O3-delta (BCZY27) HTPC electrolytes fabricated by the solid-state reactive sintering technique. Two types of devices were made; a symmetric cell used for electrode characterization, and a full fuel cell/electrolysis cell used for device performance characterization. The symmetric cell consists of a 1 mm thick BCZY27 substrate with identical air/steam electrodes on both sides. Air/steam electrodes were made by infiltrating ˜ 50 nm lanthanum nickelate nanoparticles into a BCZY27 porous backbone. The fuel cell/electrolysis cell consists of a 1mm thick Ni/BCZY27 anode support, a 25 mum thick BCZY27 electrolyte, and a 50 mum thick porous BCZY27 backbone infiltrated with lanthanum nickelate. Through symmetric cell testing, it was found that the electrode polarization resistance decreases with increasing oxygen content, indicating good oxygen reduction reaction characteristics. A minimum polarization resistance was found as 2.58 Ohm-cm2 in 3% humidied oxygen at 700 °C. Full cell testing revealed a peak power density of 27 mW-cm-2 at 700 °C. Hydrogen flux measurements were also taken in the both galvanic/post-galvanic and electrolytic operation. Galvanic/post-galvanic fluxes exhibit a very high faradaic efficiency. However, electrolytic hydrogen fluxes were much lower than the calculated hydrogen faradaic flux, indicating a different charge carrier other than protons is

  12. Thermogravimetric study of reduction of oxides present in oxidized nickel-base alloy powders

    NASA Technical Reports Server (NTRS)

    Herbell, T. P.

    1976-01-01

    Carbon, hydrogen, and hydrogen plus carbon reduction of three oxidized nickel-base alloy powders (a solid solution strengthened alloy both with and without the gamma prime formers aluminum and titanium and the solid solution strengthened alloy NiCrAlY) were evaluated by thermogravimetry. Hydrogen and hydrogen plus carbon were completely effective in reducing an alloy containing chromium, columbium, tantalum, molybdenum, and tungsten. However, with aluminum and titanium present the reduction was limited to a weight loss of about 81 percent. Carbon alone was not effective in reducing any of the alloys, and none of the reducing conditions were effective for use with NiCrAlY.

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

    SciTech Connect

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

    2013-09-07

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

  14. Oxidatively stable polyaniline derivatives for electrodes in energy storage

    NASA Astrophysics Data System (ADS)

    Lutkenhaus, Jodie; Jeon, Ju-Won; Lutkenhaus Laboratory Team

    2013-03-01

    Conjugated polymers have been explored as electrodes in batteries and pseudocapacitors for over 30 years. Yet, their widespread implementation has been hindered for several reasons such as oxidative stability, low capacity, and rate limitations associated with ionic mobility relative to current state-of-the-art. On the other hand, conjugated polymers have much to offer because of their good electronic conductivity, high Coulombic efficiency, and theoretical capacities comparable to those of metal oxides. Our lab's current goal is to overcome the aforementioned challenges, so that conjugated polymeric electrodes can be suitable used in energy storage for applications such as mechanically flexible energy storage and structural power system. This talk will present one of several experimental approaches towards synthesis and processing of polyaniline that achieve oxidatively stable, high capacity, ionically mobile electrodes. This derivative is a water-processable colloid of intimately mingled polyaniline and polyacid, where the polyacid acts as the dopant. The origin of the oxidative stability is investigated using computation modeling. This work is supported in part by the Welch Foundation.

  15. Optoelectric biosensor using indium-tin-oxide electrodes

    NASA Astrophysics Data System (ADS)

    Choi, Chang Kyoung; Kihm, Kenneth D.; English, Anthony E.

    2007-06-01

    The use of an optically thin indium-tin-oxide (ITO) electrode is presented for an optoelectric biosensor simultaneously recording optical images and microimpedance to examine time-dependent cellular growth. The transmittance of a 100nm thick ITO electrode layer is approximately the same as the transmittance of a clean glass substrate, whereas the industry-standard Au(47.5nm)/Ti(2.5nm) electrode layer drops the transmittance to less than 10% of that of the glass substrate. The simultaneous optoelectric measurements permit determining the correlation of the cell-covered area increase with the microimpedance increase, and the example results obtained for live porcine pulmonary artery endothelial cells delineate the quantitative and comprehensive nature of cellular attachment and spreading to the substrate, which has not been clearly perceived before.

  16. Electrochemical properties of inorganic nanoporous oxide coated electrodes

    NASA Astrophysics Data System (ADS)

    Leonard, Kevin C.

    The ability to produce clean water and produce and store clean energy is essential to society. Hence, technologies that facilitate clean energy and clean water are of great importance. This study focused on utilizing nanoporous insulating oxide materials to alter the chemistry at the electrode/electrolyte interface to improve the performance of a number of clean energy and clean water technologies. Here we have shown that applying a thin-film of SiO2 nanoparticles to an electrochemical capacitor electrode can increase the energy storage capacity by up to 50% at high power ratings. We have developed a geometric model to describe the coating of the porous electrode to explain the increased performance at high power ratings. We have also shown that the coated electrochemical capacitor exhibits a higher capacitance when normalized to BET surface area, suggesting that the coated surface is behaving fundamentally differently than the uncoated surface. We attribute the increase in capacitance to the inherent surface potential of the oxide coating and have shown that if we alter the surface potential of the oxide, we can in turn alter the electrochemical capacitance. In addition, we have determined that when used in capacitive deionization systems, these coatings can increase ion removal and accelerate regeneration, allowing for higher efficiency and less waste water. We have demonstrated that a nanoporous oxide coating can increase the gas production rate and lower the overpotential of the hydrogen evolution reaction via water electrolysis on both stainless steel and carbon electrodes. In addition, this work presents data on utilizing nanoporous oxide coatings on Li-Ion battery cathodes to improve high temperature capacity fade. We also introduce a novel thin-film battery/electrochemical capacitor hybrid device, which can improve the performance of simple thin-film batteries.

  17. Method of preparing a dimensionally stable electrode for use in a molten carbonate fuel cell

    DOEpatents

    Swarr, T.E.; Wnuck, W.G.

    1986-01-29

    A method is disclosed for preparing a dimensionally stable electrode structure, particularly nickel-chromium anodes, for use in a molten carbonate fuel cell stack. A low-chromium to nickel alloy is provided and oxidized in a mildly oxidizing gas of sufficient oxidation potential to oxidize chromium in the alloy structure. Typically, a steam/H/sub 2/ gas mixture in a ratio of about 100/1 and at a temperature below 800/sup 0/C is used as the oxidizing medium. This method permits the use of less than 5 wt % chromium in nickel alloy electrodes while obtaining good resistance to creep in the electrodes of a fuel cell stack.

  18. Method of preparing a dimensionally stable electrode for use in a MCFC

    DOEpatents

    Swarr, Thomas E.; Wnuck, Wayne G.

    1987-12-22

    A method is disclosed for preparing a dimensionally stable electrode structure, particularly nickel-chromium anodes, for use in a molten carbonate fuel cell stack. A low-chromium to nickel alloy is provided and oxidized in a mildly oxidizing gas of sufficient oxidation potential to oxidize chromium in the alloy structure. Typically, a steam/H.sub.2 gas mixture in a ratio of about 100/1 and at a temperature below 800.degree. C. is used as the oxidizing medium. This method permits the use of less than 5 weight percent chromium in nickel alloy electrodes while obtaining good resistance to creep in the electrodes of a fuel cell stack.

  19. Infiltrated composite electrodes for solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Buyukaksoy, Aligul

    Solid oxide fuel cells (SOFCs) are electrochemical devices which can convert chemical energy to electrical energy with efficiencies up to 60%. In order for SOFCs to be favorable energy conversion devices, the power obtained from a unit volume should be improved. This corresponds to minimized resistances from SOFC components (composite electrodes and electrolyte). Stability of the generated power is another important issue. Degradation of SOFCs with time due to microstructural processes or chemical reactions that occur at operating conditions; and due to reduction/oxidation cycles caused by the changes in the anode has been an important obstacle that has prevented the widespread commercial use of SOFCs. In this dissertation, the electrochemical properties of SOFC electrodes prepared by an infiltration technique were investigated. The long-term behavior and redox stability of the electrodes were evaluated individually and in the form of complete SOFCs. Interpretation of impedance spectra was used extensively to gain some fundamental understanding of the electrochemical properties of the electrodes along with voltammetry. Microstructural characterization was performed by electron microscopy techniques. LSM-YSZ cathodes prepared by polymeric LSM precursor infiltration resulted in cathode polarization resistance of 0.022 Ohm.cm2 at 800 °C, which then increased to 0.035 Ohm.cm2 and remained stable at this value for 100 hours. SOFCs with Ni-YSZ anodes and LSM-YSZ cathodes prepared by infiltration yielded total electrode polarizations of 0.080 Ohm.cm 2 at 800 °C. The electrode polarization resistances showed no degradation with time or upon redox cycling

  20. Highly sensitive and selective uric acid biosensor based on a three-dimensional graphene foam/indium tin oxide glass electrode.

    PubMed

    Yue, Hong Yan; Zhang, Hong; Chang, Jing; Gao, Xin; Huang, Shuo; Yao, Long Hui; Lin, Xuan Yu; Guo, Er Jun

    2015-11-01

    A three-dimensional (3D) continuous and interconnected network graphene foam (GF) was synthesized by chemical vapor deposition using nickel foam as a template. The morphologies of the GF were observed by scanning electron microscopy. X-ray diffraction and Raman spectroscopy were used to investigate the structure of GF. The graphene with few layers and defect free was closely coated on the backbone of the 3D nickel foam. After etching nickel, the GF was transferred onto indium tin oxide (ITO) glass, which acted as an electrode to detect uric acid using cyclic voltammetry (CV) and differential pulse voltammetry (DPV). The GF/ITO electrode showed a high sensitivity for the detection of uric acid: approximately 9.44 mA mM(-1) in the range of 25 nM-0.1 μM and 1.85 mA mM(-1) in the range of 0.1-60 μM. The limit of detection of GF/ITO electrode for uric acid is 3 nM. The GF/ITO electrode also showed a high selectivity for the detection of uric acid in the presence of ascorbic acid. This electrode will have a wide range of potential application prospects in electrochemical detection. Copyright © 2015. Published by Elsevier Inc.

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

    PubMed

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

    2016-01-27

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

  2. 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.

  3. 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.

  4. Sputtered iridium oxide films (SIROFs) for neural stimulation electrodes

    PubMed Central

    Cogan, Stuart F.; Ehrlich, Julia; Plante, Timothy D.; Smirnov, Anton; Shire, Douglas B.; Gingerich, Marcus; Rizzo, Joseph F.

    2009-01-01

    Sputtered iridium oxide films (SIROFs) deposited by DC reactive sputtering from an iridium metal target have been characterized in vitro for their potential as neural recording and stimulation electrodes. SIROFs were deposited over gold metallization on flexible multielectrode arrays fabricated on thin (15 µm) polyimide substrates. SIROF thickness and electrode areas of 200–1300 nm and 1960–125600 µm2, respectively, were investigated. The charge-injection capacities of the SIROFs were evaluated in an inorganic interstitial fluid model in response to charge-balanced, cathodal-first current pulses. Charge injection capacities were measured as a function of cathodal pulse width (0.2 – 1 ms) and potential bias in the interpulse period (0.0 to 0.7 V vs. Ag|AgCl). Depending on the pulse parameters and electrode area, charge-injection capacities ranged from 1–9 mC/cm2, comparable with activated iridium oxide films (AIROFs) pulsed under similar conditions. Other parameters relevant to the use of SIROF on nerve electrodes, including the thickness dependence of impedance (0.05–105 Hz) and the current necessary to maintain a bias in the interpulse region were also determined. PMID:17271216

  5. Patterning cells on optically transparent indium tin oxide electrodes.

    PubMed

    Shah, Sunny; Revzin, Alexander

    2007-01-01

    The ability to exercise precise spatial and temporal control over cell-surface interactions is an important prerequisite to the assembly of multi-cellular constructs serving as in vitro mimics of native tissues. In this study, photolithography and wet etching techniques were used to fabricate individually addressable indium tin oxide (ITO) electrodes on glass substrates. The glass substrates containing ITO microelectrodes were modified with poly(ethylene glycol) (PEG) silane to make them protein and cell resistive. Presence of insulating PEG molecules on the electrode surface was verified by cyclic voltammetry employing potassium ferricyanide as a redox reporter molecule. Importantly, the application of reductive potential caused desorption of the PEG layer, resulting in regeneration of the conductive electrode surface and appearance of typical ferricyanide redox peaks. Application of reductive potential also corresponded to switching of ITO electrode properties from cell non-adhesive to cell-adhesive. Electrochemical stripping of PEG-silane layer from ITO microelectrodes allowed for cell adhesion to take place in a spatially defined fashion, with cellular patterns corresponding closely to electrode patterns. Micropatterning of several cell types was demonstrated on these substrates. In the future, the control of the biointerfacial properties afforded by this method will allow to engineer cellular microenvironments through the assembly of three or more cell types into a precise geometric configuration on an optically transparent substrate.

  6. Structural, morphological and electrical properties of nickel oxide thin films deposited by reactive sputtering

    NASA Astrophysics Data System (ADS)

    Keraudy, J.; García Molleja, J.; Ferrec, A.; Corraze, B.; Richard-Plouet, M.; Goullet, A.; Jouan, P.-Y.

    2015-12-01

    This paper is devoted to the study of the influence of oxygen content in the nickel oxide films on the film structural, morphological and electrical properties. Nickel oxide films have been synthesized by reactive DC magnetron sputtering discharge by varying the oxygen flow rate (1.9 < Q(O2) < 3.6 sccm) for various deposition time. XRD analyses revealed the polycrystalline nature of the as-deposited films and also a phase transition from nickel oxide (1 1 1) to nickel oxide (2 0 0) associated with nickel non-stoichiometry in the NiO structure. The polycrystalline films presented an average crystallite size of 15-30 nm and a surface roughness of 1-10 nm. In-plane stress measurements have established the correlation between crystallite size and intrinsic compressive stress and also the ion-penning effect of negative oxygen ions during the film growth. A maximum stress of 10 GPa was found for lower film thickness (10 nm). By adjusting the oxygen concentration, conductive AFM (C-AFM) and resistivity measurements by the four point method have revealed at room temperature an electrical transition from insulating to conductive state. C-AFM and four point measurements showed respectively an increase in the collected current and an abrupt decrease of the mean resistivity from 107 to 10 Ω cm when the stoichiometry varies from NiO0.96 to NiO1.14. This transition is related to the non-stoichiometry attributed to nickel vacancies. Finally, low-temperature (290-100 K) electrical conduction measurements confirmed the weak dependence of Ni-deficient nickel oxide films with film thickness and showed that charge carrier conduction is a thermal-activated process.

  7. Electro-deposition of oxide-dispersed nickel composites and the behavior of their mechanical properties

    NASA Astrophysics Data System (ADS)

    Kim, Myong Jin; Kim, Joung Soo; Kim, Dong Jin; Kim, Hong Pyo

    2009-10-01

    Oxide-dispersed nickel composites were produced by electro-deposition of nickel with various types of oxide nano-powders in a sulfamate bath. The effect of the oxide concentration in the bath on the mechanical properties of the electro-deposited composites was studied. The current efficiency of the electro-deposition process was analyzed for different types of oxide nano-powders and for in terms of the amounts embedded in the nickel (Ni) matrix. To evaluate the mechanical strength and the thermal stability, micro-hardness, tensile strength and elongation were measured at room temperature for composites that were heat-treated in a temperature range of 298 K to 1123 K. The results of the experiments showed that a higher oxide powder concentration in the bath led to a greater amount of the oxide particle co-deposited in the nickel matrix. This resulted in higher micro-hardness and improved high-temperature thermal stability. However, an inhomogeneous distribution of the co-deposited oxide powders in the composites was observed to weaken the thermal stability of their tensile strength and elongation.

  8. Electrochromic properties of nickel oxide thin films prepared by the sol-gel method

    SciTech Connect

    Miki, Takeshi; Yoshimura, Kazuki; Tai, Yutaka; Tazawa, Masato; Jin, P.; Tanemura, Sakae

    1995-12-31

    Recently electrochromic (EC) device has been attractive as a smart glazing to control heating, cooling and lighting loads of buildings and housing. Among various electrochromic materials, nickel oxide is one of the typical anode type materials. Here, the electrochromic nickel oxide films were prepared onto transparent conducting film on glass substrate by the sol-gel method using an ethylene glycol solution of nickel nitrate hexahydrate. The films produced by the dip-coating method and calcined at 250, 300 and 350 C. The formed films were characterized by their electrochromic behavior in cyclic voltammetry. The formed films showed electrochromic behavior in 1M KOH aqueous solution as electrolytic solution. The cyclic voltammograms were recorded up to 100 cycles for each film. The anodic peak of the coloration reaction appeared at approximately +400 mV, while the cathodic peak of the bleaching reaction occurred at about +200 mV vs. Ag/AgCl. Both the anodic peak and the cathodic peak increased with an increase of the cyclic numbers in voltammograms, whereas these peaks at 100 cycles decreased with an increase of the calcination temperature of nickel oxide films. The calcination gave great influence on the other electrochromic behaviors of nickel oxide films.

  9. Nickel-vanadium monolayer double hydroxide for efficient electrochemical water oxidation

    NASA Astrophysics Data System (ADS)

    Fan, Ke; Chen, Hong; Ji, Yongfei; Huang, Hui; Claesson, Per Martin; Daniel, Quentin; Philippe, Bertrand; Rensmo, Håkan; Li, Fusheng; Luo, Yi; Sun, Licheng

    2016-06-01

    Highly active and low-cost electrocatalysts for water oxidation are required due to the demands on sustainable solar fuels; however, developing highly efficient catalysts to meet industrial requirements remains a challenge. Herein, we report a monolayer of nickel-vanadium-layered double hydroxide that shows a current density of 27 mA cm-2 (57 mA cm-2 after ohmic-drop correction) at an overpotential of 350 mV for water oxidation. Such performance is comparable to those of the best-performing nickel-iron-layered double hydroxides for water oxidation in alkaline media. Mechanistic studies indicate that the nickel-vanadium-layered double hydroxides can provide high intrinsic catalytic activity, mainly due to enhanced conductivity, facile electron transfer and abundant active sites. This work may expand the scope of cost-effective electrocatalysts for water splitting.

  10. Monte Carlo simulation of the oscillatory behavior in partial oxidation of methane on nickel catalyst

    NASA Astrophysics Data System (ADS)

    Ren, Xiu-Bin; Li, Huan-Ying; Guo, Xiang-Yun

    The Monte Carlo method is employed to study the kinetics of catalytic partial oxidation of methane to syngas on nickel catalyst. Using the Langmuir-Hinshelwood mechanism, self-sustained reaction rate oscillations can be observed under suitable conditions. Further analysis reveals that the rate oscillations are caused by the repetitive oxidation and reduction cycles of nickel surface, which result in a transformation of the formation mechanism of carbon monoxide from the reaction between C and O to the direct reduction of nickel oxide. The conditions for generating the self-sustained oscillations are investigated, and the regular oscillations are found for the diffusion parameter Ndif > 50 and the lattice size L ⩾ 90.

  11. Electrolytic trichloroethene degradation using mixed metal oxide coated titanium mesh electrodes.

    PubMed

    Petersen, Matthew A; Sale, Thomas C; Reardon, Kenneth F

    2007-04-01

    Electrochemical systems provide a low cost, versatile, and controllable platform to potentially treat contaminants in water, including chlorinated solvents. Relative to bare metal or noble metal amended materials, dimensionally stable electrode materials such as mixed metal oxide coated titanium (Ti/MMO) have advantages in terms of stability and cost, important factors for sustainable remediation solutions. Here, we report the use of Ti/MMO as an effective cathode substrate for treatment of trichloroethene (TCE). TCE degradation in a batch reactor was measured as the decrease of TCE concentration over time and the corresponding evolution of chloride; notably, this occurred without the formation of commonly encountered chlorinated intermediates. The reaction was initiated when Ti/MMO cathode potentials were less than -0.8 V vs. the standard hydrogen electrode, and the rate of TCE degradation increased linearly with progressively more negative potentials. The maximum pseudo-first-order heterogeneous rate constant was approximately 0.05 cm min(-1), which is comparable to more commonly used cathode materials such as nickel. In laboratory-scale flow-though column reactors designed to simulate permeable reactive barriers (PRBs), TCE concentrations were reduced by 80-90%. The extent of TCE flux reduction increased with the applied potential difference across the electrodes and was largely insensitive to the spacing distance between the electrodes. This is the first report of the electrochemical reduction of a chlorinated organic contaminant at a Ti/MMO cathode, and these results support the use of this material in PRBs as a possible approach to manage TCE plume migration.

  12. Accumulation of nickel ions in seedlings of Vicia sativa L. and manifestations of oxidative stress.

    PubMed

    Ivanishchev, V V; Abramova, E A

    2015-05-01

    The accumulation of nickel ions in the roots and shoots of vetch seedlings (Vicia sativa L.) at increasing concentrations of nickel chloride in the medium was studied. It was shown that the accumulation of nickel in the shoots was increased when the concentration of nickel chloride in the medium was more than 50 μM. The bioconcentration factor and sustainability index for vetch seedlings were calculated under the experimental conditions. The obtained results were similar to parameters for other plants, grown on a nutrient medium or soil substrate. First, the obtained results allowed estimate the limits of nickel chloride concentrations for four of five zones, which correspond to the theoretical concept of dose-response curves in the studies on the influence of physiologically essential heavy metals on plants (Prasad 2010). Some parameters of oxidative stress caused by the presence of nickel chloride in the medium were shown. It seems that at low nickel concentrations in the medium in vetch seedlings the increase of several biochemical parameters (catalase activity and proline) caused by the high amylase activity in seeds.

  13. Robust Polyoxometalate/Nickel Foam Composite Electrodes for Sustained Electrochemical Oxygen Evolution at High pH.

    PubMed

    Luo, Wenjing; Hu, Jun; Diao, Hongling; Schwarz, Benjamin; Streb, Carsten; Song, Yu-Fei

    2017-04-24

    The development of technologically viable electrodes for the electrochemical oxygen evolution reaction (OER) is a major bottleneck in chemical energy conversion. This article describes a facile one-step hydrothermal route to deposit microcrystals of a robust Dexter-Silverton polyoxometalate oxygen evolution catalyst, [Co6.8 Ni1.2 W12 O42 (OH)4 (H2 O)8 ], on a commercial nickel foam electrode. The electrode shows efficient and sustained electrochemical oxygen evolution at low overpotentials (360 mV at 10 mA cm(-2) against RHE, Tafel slope 126 mV dec(-1) , faradaic efficiency (96±5) %) in alkaline aqueous solution (pH 13). Post-catalytic analyses show no mechanical or chemical degradation and no physical detachment of the microcrystals. The results provide a blueprint for the stable "wiring" of POM catalysts to commercial metal foam substrates, thus giving access to technologically relevant composite OER electrodes. © 2017 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim.

  14. Synthesis and characterization of bis nitrato[4-hydroxyacetophenonesemicarbazone) nickel(II) complex as ionophore for thiocyanate-selective electrode.

    PubMed

    Chandra, Sulekh; Hooda, Sunita; Tomar, Praveen Kumar; Malik, Amrita; Kumar, Ankit; Malik, Sakshi; Gautam, Seema

    2016-05-01

    The PVC based-ion selective electrode viz., bis nitrato[4-hydroxyacetophenone semicarbazone] nickel(II) as an ionophore was prepared for the determination of thiocyanate ion. The ionophore was characterized by FT-IR, UV-vis, XRD, magnetic moment and elemental analysis (CHN). On the basis of spectral studies an octahedral geometry has been assigned. The best performance was obtained with a membrane composition of 31% PVC, 63% 2-nitrophenyl octylether, 4.0% ionophore and 2.0% trioctylmethyl ammonium chloride. The electrode exhibited an excellent Nernstian response to SCN(-) ion ranging from 1.0 × 10(-7) to 1.0 × 10(-1)M with a detection limit of 8.6 × 10(-8)M and a slope of -59.4 ± 0.2 mV/decade over a wide pH range (1.8-10.7) with a fast response time (6s) at 25 °C. The proposed electrode showed high selectivity for thiocyanate ion over a number of common inorganic and organic anions. It was successfully applied to direct determination of thiocyanate in biological (urine and saliva) samples in order to distinguish between smokers and non-smokers, environmental samples and as an indicator electrode for titration of thiocyanate ions with AgNO3 solution. Copyright © 2016 Elsevier B.V. All rights reserved.

  15. Real time charge efficiency monitoring for nickel electrodes in NICD and NIH2 cells

    NASA Technical Reports Server (NTRS)

    Zimmerman, A. H.

    1987-01-01

    The charge efficiency of nickel-cadmium and nickel-hydrogen battery cells is critical in spacecraft applications for determining the amount of time required for a battery to reach a full state of charge. As the nickel-cadmium or nickel-hydrogen batteries approach about 90 percent state of charge, the charge efficiency begins to drop towards zero, making estimation of the total amount of stored charge uncertain. Charge efficiency estimates are typically based on prior history of available capacity following standardized conditions for charge and discharge. These methods work well as long as performance does not change significantly. A relatively simple method for determining charge efficiencies during real time operation for these battery cells would be a tremendous advantage. Such a method was explored and appears to be quite well suited for application to nickel-cadmium and nickel-hydrogen battery cells. The charge efficiency is monitored in real time, using only voltage measurements as inputs. With further evaluation such a method may provide a means to better manage charge control of batteries, particularly in systems where a high degree of autonomy or system intelligence is required.

  16. One-Step Growth of Iron-Nickel Bimetallic Nanoparticles on FeNi Alloy Foils: Highly Efficient Advanced Electrodes for the Oxygen Evolution Reaction.

    PubMed

    Qazi, Umair Yaqub; Yuan, Cheng-Zong; Ullah, Naseeb; Jiang, Yi-Fan; Imran, Muhammad; Zeb, Akif; Zhao, Sheng-Jie; Javaid, Rahat; Xu, An-Wu

    2017-08-30

    Electrochemical water splitting is an important process to produce hydrogen and oxygen for energy storage and conversion devices. However, it is often restricted by the oxygen evolution reaction (OER) due to its sluggish kinetics. To overcome the problem, precious metal oxide-based electrocatalysts, such as RuO2 and IrO2, are widely used. The lack of availability and the high cost of precious metals compel researchers to find other resources for the development of cost-effective, environmentally friendly, earth-abundant, nonprecious electrocatalysts for OER. Such catalysts should have high OER performance and good stability in comparison to those of available commercial precious metal-based electrocatalysts. Herein, we report an inexpensive fabrication of bimetallic iron-nickel nanoparticles on FeNi-foil (FeNi4.34@FeNi-foil) as an integrated OER electrode using a one-step calcination process. FeNi4.34@FeNi-foil obtained at 900 °C shows superior OER activity in alkaline solution with an overpotential as low as 283 mV to achieve a current density of 10 mA cm(-2) and a small Tafel slope of 53 mV dec(-1). The high performance and durability of the as-prepared nonprecious metal electrode even exceeds those of the available commercial RuO2 and IrO2 catalysts, showing great potential in replacing the expensive noble metal-based electrocatalysts for OER.

  17. Preparation and characterization of copper-doped cobalt oxide electrodes.

    PubMed

    Rosa-Toro, A La; Berenguer, R; Quijada, C; Montilla, F; Morallón, E; Vazquez, J L

    2006-11-30

    Cobalt oxide (Co3O4) and copper-doped cobalt oxide (CuxCo(3-x)O4) films have been prepared onto titanium support by the thermal decomposition method. The electrodes have been characterized by different techniques such as cyclic voltammetry, scanning electron microscopy, X-ray diffraction, and X-ray photoelectron spectroscopy (XPS). The effect on the electrochemical and crystallographic properties and surface morphology of the amount of copper in the oxide layer has been analyzed. The XPS spectra correspond to a characteristic monophasic Cu-Co spinel oxides when x is below 1. However, when the copper content exceeds that for the stoichiometric CuCo2O4 spinel, a new CuO phase segregates at the surface. The analysis of the surface cation distribution indicates that Cu(II) has preference for octahedral sites.

  18. Gold-TiO2-Nickel catalysts for low temperature-driven CO oxidation reaction

    NASA Astrophysics Data System (ADS)

    Hinojosa-Reyes, Mariana; Zanella, Rodolfo; Maturano-Rojas, Viridiana; Rodríguez-González, Vicente

    2016-04-01

    Nickel-doped-TiO2 catalysts were prepared by the sol-gel method and surface modified with gold nanoparticles (AuNPs) by the urea-deposition-precipitation technique. The as-synthesized catalysts were characterized by X-ray diffraction, Raman and XPS spectroscopies, N2 physisorption, STEM-HAADF microscopy and TPR hydrogen consumption. The Au/TiO2-Ni catalysts were evaluated catalytically performing CO oxidation reactions. The catalyst with nickel content of 1 wt. % (Au/TiO2-Ni 1) showed the highest CO conversion with respect to the high-nickel-content or bare/commercial TiO2 at 0 °C. In situ DRIFTS showed a strong participation of both nickel due to the presence of surface-nickel-metallic nanoparticles formed during the CO adsorption process at reaction temperatures above 200 °C, and surface-bridged-nickel-CO species. A minor deactivation rate was observed for the Au/TiO2-Ni 1 catalyst in comparison with the Au/TiO2 one. The oxygen vacancies that were created on the sol-gel-doped TiO2 improved the catalytic behavior during the performance of CO oxidation reactions, and inhibited the AuNP sintering.

  19. Nonlinear refraction properties of nickel oxide thin films at 800 nm

    SciTech Connect

    Melo, Ronaldo P. Jr. de; Silva, Blenio J. P. da; Santos, Francisco Eroni P. dos; Azevedo, A.; Araujo, Cid B. de

    2009-11-01

    Measurements of the nonlinear refractive index, n{sub 2}, of nickel oxide films prepared by controlled oxidation of nickel films deposited on substrates of soda-lime glass are reported. The structure and morphology of the samples were characterized by scanning electron microscopy, atomic force microscopy, and x-ray diffractometry. Samples of excellent optical quality were prepared. The nonlinear measurements were performed using the thermally managed eclipse Z-scan technique at 800 nm. A large value of n{sub 2}approx =10{sup -12} cm{sup 2}/W and negligible nonlinear absorption were obtained.

  20. Porous electrode preparation method

    DOEpatents

    Arons, R.M.; Dusek, J.T.

    1983-10-18

    A porous sintered plaque is provided with a bimodal porosity that is especially well suited for use as an electrode within a molten carbonate fuel cell. The coarse porosity is sufficient for admitting gases into contact with the reaction surfaces while the fine porosity is wetted with and retains molten electrolyte on the reaction sites. The electrode structure is prepared by providing a very fine powder of such as nickel oxide and blending the powder with a suitable decomposable binder to form a solid mass. The mass is comminuted into agglomerate size particles substantially larger than the fine oxide particles and formed into a cohesive compact for subsequent sintering. Sintering is carried out at sufficient conditions to bind the agglomerates together into a porous structure having both coarse and fine porosity. Where lithiated nickel oxide cathodes are prepared, the sintering conditions can be moderate enough to retain substantial quantities of lithium within the electrode for adequate conductivity. 2 figs.

  1. Porous electrode preparation method

    DOEpatents

    Arons, Richard M.; Dusek, Joseph T.

    1983-01-01

    A porous sintered plaque is provided with a bimodal porosity that is especially well suited for use as an electrode within a molten carbonate fuel cell. The coarse porosity is sufficient for admitting gases into contact with the reaction surfaces while the fine porosity is wetted with and retains molten electrolyte on the reaction sites. The electrode structure is prepared by providing a very fine powder of such as nickel oxide and blending the powder with a suitable decomposable binder to form a solid mass. The mass is comminuted into agglomerate size particles substantially larger than the fine oxide particles and formed into a cohesive compact for subsequent sintering. Sintering is carried out at sufficient conditions to bind the agglomerates together into a porous structure having both coarse and fine porosity. Where lithiated nickel oxide cathodes are prepared, the sintering conditions can be moderate enough to retain substantial quantities of lithium within the electrode for adequate conductivity.

  2. A method for making an alkaline battery electrode plate

    NASA Technical Reports Server (NTRS)

    Chida, K.; Ezaki, T.

    1983-01-01

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

  3. Enhancement of the analytical properties and catalytic activity of a nickel hexacyanoferrate modified carbon ceramic electrode prepared by two-step sol-gel technique: application to amperometric detection of hydrazine and hydroxyl amine.

    PubMed

    Salimi, Abdollah; Abdi, Kamaleddin

    2004-05-28

    The electroless sol-gel technique was used for the construction of nickel hexacyanoferrat (NiHCF) modified carbon composite electrodes (CCEs).This involves two steps: formation of a carbon ceramic electrode fabricated by nickel powder and then immersing the electrode into a sodium- hexacyanoferate solution for the immobilization of NiHCF films. The cyclic voltammety of the resulting modified CCEs prepared under optimum conditions, shows a well defined surface redox couple due to the [Ni(II)Fe(III/II)(CN)(6)](-2/-1) system. The effect of different alkali metal cations in supporting electrolyte on the behavior of the modified electrode were studied. The charge transfer coefficient (alpha) and charge transfer rate constant (k(s)) for modified films were calculated. Hydrazine and hydroxylamine have been chosen as a model to elucidate the electocatalytic ability and analytical parameters of NiHCF modified CCE prepared by one and two-step sol-gel techniques and these compounds determined amperometically at the surface of modified electrodes. The latter shows a good electocatalytic activity towards the oxidation of hydrazine and hydroxylamine in the pH range 3-8 in comparison with CCEs modified by homogeneous mixture of graphite powder, Ni(NO(3))(2) and Na(2)[Fe(CN)(6)], (one-step sol-gel technique). Furthermore, the catalytic rate constant, linear dynamic range, limit of detection, and sensitivity for hydrazine and hydroxylamine detections were evaluated and compared with CCEs prepared with one-step sol-gel method. The modified CCEs containing NiHCF shows good repeatability, short response time, t 90%<3s, long term stability (3 months) and excellent catalytic activity. Furthermore, the method of preparation is rapid and simple and the modified electrodes are renewed by simple mechanical polishing and immersing in [Na(3)Fe(CN](6)] solution.

  4. Lithium Metal Oxide Electrodes For Lithium Cells And Batteries

    DOEpatents

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

    2004-01-20

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

  5. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2008-12-23

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

  6. Formation of nickel-manganese oxide thermistors studied by XRD, SEM and auger spectroscopy

    NASA Astrophysics Data System (ADS)

    Azimi-Nam, S.; Golestani-Fard, F.; Hashemi, T.

    1987-03-01

    This paper describes the formation of nickel-manganeses oxide thermistor bodies at 1000 1340° C, employing analytical techniques of XRD, SEM/EPMA and AES. The micro-structural studies revealed that the main phase of nickel manganite coexists with a solid solution of NiO in Mn3O4 in the final product. The optimum firing conditions to achieve the necessary electrical properties as well as the development of the desired microstructure could be selected around 1200° C, for 4 hrs in an ambient atmosphere. Above this temperature, the density begins to decrease while the resistivity increases. These anomalous electrical resistivity variations could be partly attributed to the trapped oxygen which was evolved from the decomposition of the unreacted α-Mn2O3. At-lower temperatures, unreacted nickel oxide residuals as well as a high porosity of the samples would yield specimens with high resistivity.

  7. Ionic Liquid Doped β Lactoglobulin as Template for Nanoclusters of Nickel Oxide

    NASA Astrophysics Data System (ADS)

    Sankaranarayanan, Kamatchi; Kalaiyarasi, M.; Sreedhar, B.; Nair, B. U.; Dhathathreyan, A.

    2014-03-01

    In this work, Langmuir films of organized assemblies of β-lactoglobulin (βLG) with 1-ethyl-3-methyl imidazolium ethyl sulfate (IL-emes) have been characterized at air/water interface using surface pressure-specific area isotherms and dilational rheology. The protein in the IL-mediated assembly shows excellent packing at the interface and is stable as seen in circular dichroic spectroscopy. These spread films on nickel chloride were transferred as Langmuir-Schaffer films of βLG and βLG+IL-emes and used as template for designing nanoclusters of nickel oxide. The nanoclusters have been characterized using transmission electron microscopy (TEM) and powder XRD. While pure protein template gives needle-shaped structures, the IL-mediated template gives spherical shapes of hexagonal nickel oxide in the range 30 nm to 40 nm. Presence of ionic liquid seems to slow down the growth of the cluster and also prevents aggregation of the clusters.

  8. Studies of reaction geometry in oxidation and reduction of the alkaline silver electrode

    NASA Technical Reports Server (NTRS)

    Butler, E. A.; Blackham, A. U.

    1971-01-01

    Two methods of surface area estimations of sintered silver electrodes have given roughness factors of 58 and 81. One method is based on constant current oxidation, the other is based on potentiostatic oxidation. Examination of both wire and sintered silver electrodes via scanning electron microscopy at various stages of oxidation have shown that important structural features are mounds of oxide. In potentiostatic oxidations these appear to form on sites instantaneously nucleated while in constant current oxidations progressive nucleation is indicated.

  9. Development of a Lead-free Piezoelectric (K,Na)NbO3 Thin Film Deposited on Nickel-based Electrodes

    NASA Astrophysics Data System (ADS)

    Bani Milhim, Alaeddin

    It is desirable to replace noble metals used as electrode materials for piezoelectric thin film with base metals. This will reduce the piezoelectric thin film fabrication cost. A nickel?based layer in conjunction with other protective layers is proposed as a bottom electrode for lead-free piezoelectric KNN thin film. The obtained results do not indicate the oxidation of the nickel?based bottom electrode after the deposition of KNN at 600 °C for 10 hours in the presence of oxygen and/or after annealing the sample at 400 °C for an hour in air. The fabricated KNN thin film was fully characterized in this work. The effective piezoelectric coefficients d33 and d31 were estimated to be 37 pm/V and 17.2 pm/V, respectively, at 100 kV/cm. The piezoelectric properties of the fabricated KNN/Ni/Ti/SiO2/Si are affected by the crystal orientation of the KNN layer, which was preferentially oriented in the (110) direction. Optimization of the deposition parameters of the fabricated KNN/Ni/Ti/SiO2/Si film is expected to further enhance the piezoelectric properties. Two novel systems utilizing the developed KNN piezoelectric thin film are proposed and their performance simulated based on the achieved KNN thin film parameters. The first is a precision automated nanomanipulation system using an AFM as a sensor and piezo-actuated manipulators. Real-time feedback of the particle being manipulated can be achieved using the proposed system. The length of the manipulators needs to be at least 2 mm to be incorporated with a commercial AFM system. To fabricate the required manipulators, a three-step electrochemical etching technique was developed. Tungsten tips combining well-defined conical shape, a length as large as 2 mm, and sharpness with a radius of curvature of around 20 nm were fabricated using the proposed technique. By depositing the KNN thin film on the fabricated manipulator, nanomanipulators with out-of-plane actuation can be produced. Ultrasonic piezoelectric fan array, the

  10. Kinetics of ethanol oxidation on electroless Ni-P/SnO{sub 2}/Ti electrodes in KOH solutions

    SciTech Connect

    Lo, Y.L.; Hwang, B.J.

    1995-02-01

    The electrolytic oxidation of ethanol was investigated on the electroless Ni-P/SnO{sub 2}/Ti electrodes in 1M KOH. The mechanisms of ethanol oxidation on the electrode were studied via cyclic voltammetry and polarization curves. The kinetic equations were derived, and the kinetic parameters were obtained from a comparison of experimental results and the kinetic equations. The redox reaction of the nickel electrode in the alkaline-solution is reversible, and the rate constants related to this reaction, k{sub 1} as well as k{sub {minus}1}, are functions of applied potential. Ethanol oxidation on the electroless Ni-P/SnO{sub 2}/Ti is through a chemical reaction with a rate constant k{sub c1}. These rate constants were determined from the current-potential curves and the kinetic model at various concentrations of ethanol. The rate constants for electrochemical reaction could be expressed as k{sub 1} (E) = 8.892 {times} 10{sup {minus}13} exp (0.6525FE/RT) s{sup {minus}1}, k{sub {minus}1} (E) = 8,034 {times} 10{sup {minus}6} exp ({minus}0.3475FE/RT) where E was the applied potential vs. Ag/AgCl, and the chemical reaction rate constant (k{sub cl}) was 5.822 {times} 10{sup {minus}6} dm{sup 3}/mol {times} s.

  11. Visibility and oxidation stability of hybrid-type copper mesh electrodes with combined nickel–carbon nanotube coating

    NASA Astrophysics Data System (ADS)

    Kim, Bu-Jong; Hwang, Young-Jin; Park, Jin-Seok

    2017-04-01

    Hybrid-type transparent conductive electrodes (TCEs) were fabricated by coating copper (Cu) meshes with carbon nanotube (CNT) via electrophoretic deposition, and with nickel (Ni) via electroplating. For the fabricated electrodes, the effects of the coating with CNT and Ni on their transmittance and reflectance in the visible-light range, electrical sheet resistance, and chromatic parameters (e.g., redness and yellowness) were characterized. Also, an oxidation stability test was performed by exposing the electrodes to air for 20 d at 85 °C and 85% temperature and humidity conditions, respectively. It was discovered that the CNT coating considerably reduced the reflectance of the Cu meshes, and that the Ni coating effectively protected the Cu meshes against oxidation. Furthermore, after the coating with CNT, both the redness and yellowness of the Cu mesh regardless of the Ni coating approached almost zero, indicating a natural color. The experiment results confirmed that the hybrid-type Cu meshes with combined Ni-CNT coating improved characteristics in terms of reflectance, sheet resistance, oxidation stability, and color, superior to those of the primitive Cu mesh, and also simultaneously satisfied most of the requirements for TCEs.

  12. The synthesis, characterization and reactivity of high oxidation state nickel fluorides

    SciTech Connect

    Chacon, L.C. |

    1997-12-01

    The research described in this thesis has mainly addressed the challenge of the synthesis of thermodynamically unstable nickel fluorides, which cannot be made by traditional thermal methods. A low-temperature approach towards the synthesis of such transition metal fluorides exploits the greater thermodynamic stability of high oxidation states in anions and involves the use of anhydrous hydrogen fluoride (aHF) as a solvent. The general method consists of combining an aHF soluble starting material (e.g., K{sub 2}NiF{sub 6}) with a Lewis fluoroacid (e.g., BF{sub 3}), which precipitates a neutral polymeric solid state fluoride: 2 K{sup +} + NiF{sub 6}{sup 2{minus}} + BF{sub 3} {r_arrow} NiF{sub 4} + 2 BF{sub 4}{sup {minus}} + 2 K{sup +}. At room temperature, this reaction yields a different structural phase, with composition K{sub x}NiF{sub 3} (x {approx} 0.18). This material has a pseudo-hexagonal tungsten bronze structure (H{sub 0}-K{sub x}NiF{sub 3}), and is an ionic conductor, probably due to K{sup +} ions hosted in the lattice channels. R-NiF{sub 3} is capable of fluorinating a wide range of inorganic and organic substrates. These reactions have probably shed light on the mechanism of the Simons Electrochemical Fluorination (ECF) Process, an important industrial method of fluorinating organic compounds. It has long been speculated that NiF{sub 3} plays a role in the ECF process, which uses nickel electrodes in aHF solvent. K{sub 2}NiF{sub 6} also fluorinates organic compounds in aHF, but interestingly, yields different fluorinated products. The reduction of R-NiF{sub 3} and K{sub 2}NiF{sub 6} during fluorination reactions yields NiF{sub 2}. A method has been developed to regenerate NiF{sub 6}{sup 2{minus}} from NiF{sub 2}.

  13. Nanohoneycomb-like manganese cobalt sulfide/three dimensional graphene-nickel foam hybid electrodes for high-rate capability supercapacitors

    NASA Astrophysics Data System (ADS)

    Yu, Mei; Li, Xinjie; Ma, Yuxiao; Liu, Ruili; Liu, Jianhua; Li, Songmei

    2017-02-01

    Nanohoneycomb-like manganese cobalt sulfide/three dimensional graphene-nickel foam hybrid electrodes for supercapacitor are synthesized by chemical vapor deposition and electrodeposition. The ternary sulfide electrode exhibits high specific capacitance (1938 F g-1 at 5 A g-1) with excellent rate capability (76.8% capacitance retention at 100 A g-1) due to the intercrossed feature of the nanowalls and three-dimensional interpenetrating nanoarchitecture. Moreover, the specific capacitance of the electrode after 4000 cycles at a high current density of 50 A g-1 is 1320 F g-1. The asymmetric supercapacitor assembled with the manganese cobalt sulfide electrode and an activated carbon electrode displays an energy density of 14.33 W h kg-1 at a power density of 74.87 W kg-1. The manganese cobalt sulfide is a promising electrode material for practical application.

  14. Electrochromic nickel oxide simultaneously doped with lithium and a metal dopant

    DOEpatents

    Gillaspie, Dane T.; Weir, Douglas Glenn John

    2017-05-16

    An electrochromic device comprising a counter electrode layer comprised of lithium metal oxide which provides a high transmission in the fully intercalated state and which is capable of long-term stability, is disclosed. Methods of making an electrochromic device comprising such a counter electrode are also disclosed.

  15. Electrochromic nickel oxide simultaneously doped with lithium and a metal dopant

    DOEpatents

    Gillaspie, Dane T; Weir, Douglas G

    2014-04-01

    An electrochromic device comprising a counter electrode layer comprised of lithium metal oxide which provides a high transmission in the fully intercalated state and which is capable of long-term stability, is disclosed. Methods of making an electrochromic device comprising such a counter electrode are also disclosed.

  16. Amperometric detection and electrochemical oxidation of aliphatic amines and ammonia on silver-lead oxide thin-film electrodes

    SciTech Connect

    Ge, Jisheng

    1996-01-08

    This thesis comprises three parts: Electrocatalysis of anodic oxygen-transfer reactions: aliphatic amines at mixed Ag-Pb oxide thin-film electrodes; oxidation of ammonia at anodized Ag-Pb eutectic alloy electrodes; and temperature effects on oxidation of ethylamine, alanine, and aquated ammonia.

  17. Catalytic Activity and Impedance Behavior of Screen-Printed Nickel Oxide as Efficient Water Oxidation Catalysts.

    PubMed

    Singh, Archana; Fekete, Monika; Gengenbach, Thomas; Simonov, Alexandr N; Hocking, Rosalie K; Chang, Shery L Y; Rothmann, Mathias; Powar, Satvasheel; Fu, Dongchuan; Hu, Zheng; Wu, Qiang; Cheng, Yi-Bing; Bach, Udo; Spiccia, Leone

    2015-12-21

    We report that films screen printed from nickel oxide (NiO) nanoparticles and microballs are efficient electrocatalysts for water oxidation under near-neutral and alkaline conditions. Investigations of the composition and structure of the screen-printed films by X-ray diffraction, X-ray absorption spectroscopy, and scanning electron microscopy confirmed that the material was present as the cubic NiO phase. Comparison of the catalytic activity of the microball films to that of films fabricated by using NiO nanoparticles, under similar experimental conditions, revealed that the microball films outperform nanoparticle films of similar thickness owing to a more porous structure and higher surface area. A thinner, less-resistive NiO nanoparticle film, however, was found to have higher activity per Ni atom. Anodization in borate buffer significantly improved the activity of all three films. X-ray photoelectron spectroscopy showed that during anodization, a mixed nickel oxyhydroxide phase formed on the surface of all films, which could account for the improved activity. Impedance spectroscopy revealed that surface traps contribute significantly to the resistance of the NiO films. On anodization, the trap state resistance of all films was reduced, which led to significant improvements in activity. In 1.00 m NaOH, both the microball and nanoparticle films exhibit high long-term stability and produce a stable current density of approximately 30 mA cm(-2) at 600 mV overpotential. © 2015 WILEY-VCH Verlag GmbH & Co. KGaA, Weinheim.

  18. Fabrication Process of Fine Electrodes Using Shadow Mask Evaporation and Tip-Induced Local Oxidation

    NASA Astrophysics Data System (ADS)

    Akai, Tomonori; Abe, Takumi; Ishibashi, Masayoshi; Kato, Midori; Heike, Seiji; Shimomura, Takeshi; Okai, Makoto; Hashizume, Tomihiro; Ito, Kohzo

    2002-07-01

    We report on a simple process for fabricating fine electrodes by using shadow mask evaporation and tip-induced local oxidation. A set of electrodes for four-term resistance measurement has been fabricated. The gap width between the fine electrode was 150 nm and the roughness of the electrode surface was less than 0.5 nm. We were able to use the electrodes to measure the conductivity of a multiwalled carbon nanotube (MWNT).

  19. Molten metal electrodes in solid oxide fuel cells

    NASA Astrophysics Data System (ADS)

    Javadekar, Ashay Dileep

    Molten metal electrodes in solid oxide fuel cells are electrochemically characterized for their possible use in direct carbon oxidation and energy storage. The cells were operated in the battery mode at 973 K, without added fuel, in order to understand the oxidation characteristics of Sb alloys as anodes at electrolyte interfaces. The cells using 50-mol% In-Sb and Sn-Sb mixtures exhibited open-circuit voltages (OCV) of 1.0 and 0.93 V, values similar to those of cells with pure In and Sn anodes respectively, and insulating In2O3 and SnO2 layers formed at the electrolyte interface. The 50-mol% Sb-Bi cell had an OCV of 0.73 V initially, close to that with pure Sb anode. The OCV remained constant until all of the Sb had been oxidized, after which it dropped to 0.43 V, similar to the value for pure Bi. SEM analysis of the spent cell showed two distinct phases, with metallic Bi at the bottom and Sb2O3 at the top. The cell with 50-mol% Sb-Pb anode exhibited an OCV that changed continuously with conversion, from 0.73 V initially to 0.67 V following the addition of charge equivalent to oxidation of 120% the Sb. The total cell impedance remained low for this entire period. EDS measurements on the sectioned Sb-Pb cell suggested formation of a mixed oxide of Pb and Sb. An energy-storage concept using molten Sb as the fuel in a reversible solid-oxide electrochemical cell was tested using a button cell with a Sc-stabilized zirconia electrolyte at 973 K, by measuring the impedances under fuel-cell and electrolyzer conditions for a range of stirred Sb-Sb2O 3 compositions. The Sb-Sb2O3 electrode impedances were found to be on the order of 0.15 ohm.cm2 for both fuel-cell and electrolyzer conditions, for compositions up to 30% Sb and 70% Sb2O3. The OCVs were 0.75 V, independent of conversion. The use of molten neat Ag and alloyed Ag-Sb for direct-carbon anodes in SOFCs has been examined at 1273 K. For Ag, an OCV typical of that expected for carbon oxidation, 1.12 V, was observed when

  20. Solvothermal synthesis of NiAl double hydroxide microspheres on a nickel foam-graphene as an electrode material for pseudo-capacitors

    SciTech Connect

    Momodu, Damilola; Bello, Abdulhakeem; Dangbegnon, Julien; Barzeger, Farshad; Taghizadeh, Fatimeh; Fabiane, Mopeli; Manyala, Ncholu; Johnson, A. T. Charlie

    2014-09-15

    In this paper, we demonstrate excellent pseudo-capacitance behavior of nickel-aluminum double hydroxide microspheres (NiAl DHM) synthesized by a facile solvothermal technique using tertbutanol as a structure-directing agent on nickel foam-graphene (NF-G) current collector as compared to use of nickel foam current collector alone. The structure and surface morphology were studied by X-ray diffraction analysis, Raman spectroscopy and scanning and transmission electron microscopies respectively. NF-G current collector was fabricated by chemical vapor deposition followed by an ex situ coating method of NiAl DHM active material which forms a composite electrode. The pseudocapacitive performance of the composite electrode was investigated by cyclic voltammetry, constant charge–discharge and electrochemical impedance spectroscopy measurements. The composite electrode with the NF-G current collector exhibits an enhanced electrochemical performance due to the presence of the conductive graphene layer on the nickel foam and gives a specific capacitance of 1252 F g{sup −1} at a current density of 1 A g{sup −1} and a capacitive retention of about 97% after 1000 charge–discharge cycles. This shows that these composites are promising electrode materials for energy storage devices.

  1. Mechanism of sodium chloride in promoting reduction of high-magnesium low-nickel oxide ore.

    PubMed

    Zhou, Shiwei; Wei, Yonggang; Li, Bo; Wang, Hua; Ma, Baozhong; Wang, Chengyan

    2016-07-04

    Sodium chloride has been proved that it is an effective promoter for the reduction of high-magnesium, low-nickel oxide ore. The aim of current work is to clarify the promotion behavior of sodium chloride in the roasting reduction process. The influence of moisture on the reduction of ore in the presence of sodium chloride is studied to get clear comprehension of promotion process. In the presence of moisture, the HCl is produced by pyrohydrolysis of sodium chloride for chlorinating nickel and iron oxides, moreover, interactions between metallic oxides and sodium chloride are also a way for chlorination at high temperature (>802 °C); subsequently, the metal chloride would be reduced by reductant. In the absence of moisture, the magnetic separation results show that the recoveries of iron and nickel have a significant increase; moreover, olivine structure would be destroyed gradually with the increase of roasting temperature in the action of sodium chloride, and the sodium chloride existed in high-magnesium, low-nickel oxide ore could make the NiO isolate from NiO-bearing minerals. The NiO reacts with Fe2O3 at high temperature to form NiFe2O4, which is conductive to the formation of Ni-Fe alloy during the reduction process.

  2. Mechanism of sodium chloride in promoting reduction of high-magnesium low-nickel oxide ore

    PubMed Central

    Zhou, Shiwei; Wei, Yonggang; Li, Bo; Wang, Hua; Ma, Baozhong; Wang, Chengyan

    2016-01-01

    Sodium chloride has been proved that it is an effective promoter for the reduction of high-magnesium, low-nickel oxide ore. The aim of current work is to clarify the promotion behavior of sodium chloride in the roasting reduction process. The influence of moisture on the reduction of ore in the presence of sodium chloride is studied to get clear comprehension of promotion process. In the presence of moisture, the HCl is produced by pyrohydrolysis of sodium chloride for chlorinating nickel and iron oxides, moreover, interactions between metallic oxides and sodium chloride are also a way for chlorination at high temperature (>802 °C); subsequently, the metal chloride would be reduced by reductant. In the absence of moisture, the magnetic separation results show that the recoveries of iron and nickel have a significant increase; moreover, olivine structure would be destroyed gradually with the increase of roasting temperature in the action of sodium chloride, and the sodium chloride existed in high-magnesium, low-nickel oxide ore could make the NiO isolate from NiO-bearing minerals. The NiO reacts with Fe2O3 at high temperature to form NiFe2O4, which is conductive to the formation of Ni-Fe alloy during the reduction process. PMID:27374991

  3. Mechanism of sodium chloride in promoting reduction of high-magnesium low-nickel oxide ore

    NASA Astrophysics Data System (ADS)

    Zhou, Shiwei; Wei, Yonggang; Li, Bo; Wang, Hua; Ma, Baozhong; Wang, Chengyan

    2016-07-01

    Sodium chloride has been proved that it is an effective promoter for the reduction of high-magnesium, low-nickel oxide ore. The aim of current work is to clarify the promotion behavior of sodium chloride in the roasting reduction process. The influence of moisture on the reduction of ore in the presence of sodium chloride is studied to get clear comprehension of promotion process. In the presence of moisture, the HCl is produced by pyrohydrolysis of sodium chloride for chlorinating nickel and iron oxides, moreover, interactions between metallic oxides and sodium chloride are also a way for chlorination at high temperature (>802 °C) subsequently, the metal chloride would be reduced by reductant. In the absence of moisture, the magnetic separation results show that the recoveries of iron and nickel have a significant increase; moreover, olivine structure would be destroyed gradually with the increase of roasting temperature in the action of sodium chloride, and the sodium chloride existed in high-magnesium, low-nickel oxide ore could make the NiO isolate from NiO-bearing minerals. The NiO reacts with Fe2O3 at high temperature to form NiFe2O4, which is conductive to the formation of Ni-Fe alloy during the reduction process.

  4. Effect of Co/Ni ratios in cobalt nickel mixed oxide catalysts on methane combustion

    SciTech Connect

    Lim, Tae Hwan; Cho, Sung June; Yang, Hee Sung; Engelhard, Mark H.; Kim, Do Heui

    2015-07-31

    A series of cobalt nickel mixed oxide catalysts with the varying ratios of Co to Ni, prepared by co-precipitation method, were applied to methane combustion. Among the various ratios, cobalt nickel mixed oxides having the ratios of Co to Ni of (50:50) and (67:33) demonstrate the highest activity for methane combustion. Structural analysis obtained from X-ray diffraction (XRD) and extended X-ray absorption fine structure (EXAFS) evidently demonstrates that CoNi (50:50) and (67:33) samples consist of NiCo2O4and NiO phase and, more importantly, NiCo2O4spinel structure is largely distorted, which is attributed to the insertion of Ni2+ions into octahedral sites in Co3O4spinel structure. Such structural dis-order results in the enhanced portion of surface oxygen species, thus leading to the improved reducibility of the catalysts in the low temperature region as evidenced by temperature programmed reduction by hydrogen (H2TPR) and X-ray photoelectron spectroscopy (XPS) O 1s results. They prove that structural disorder in cobalt nickel mixed oxides enhances the catalytic performance for methane combustion. Thus, it is concluded that a strong relationship between structural property and activity in cobalt nickel mixed oxide for methane combustion exists and, more importantly, distorted NiCo2O4spinel structure is found to be an active site for methane combustion.

  5. Nickel/magnesium-lanthanum mixed oxide catalyst in the Kumada-coupling.

    PubMed

    Kiss, Arpád; Hell, Zoltán; Bálint, Mária

    2010-01-21

    A new, heterogeneous, magnesium-lanthanum mixed oxide solid base-supported nickel(ii) catalyst was developed. The catalyst was used successfully in the Kumada coupling of aryl halides, especially aryl bromides. The optimal reaction conditions of the coupling were determined.

  6. Smart nickel oxide materials for the applications of energy efficiency and storage

    NASA Astrophysics Data System (ADS)

    Lin, Feng

    The present dissertation studies nickel oxide-based materials for the application of electrochromic windows and lithium-air batteries. The materials were fabricated via radio frequency magnetron sputtering and subsequently post-treated with thermal evaporation and ozone exposure. The strategies to improve electrochromic performance of nickel oxide materials were investigated including compositional control, morphology tuning, modification of electronic structure and interface engineering (i.e., Li2O 2, graphene). The electrochemical properties of the resulting materials were characterized in lithium ion electrolytes. Extremely high performing nickel oxide-based electrochromic materials were obtained in terms of optical modulation, switching kinetics, bleached-state transparency and durability, which promise the implementation of these materials for practical smart windows. With the aid of advanced synchrotron X-ray absorption spectroscopy, it is reported for the first time that the electrochromic effect in multicomponent nickel oxide-based materials arises from the reversible formation of hole states in the NiO6 cluster accompanying with the reversible formation of Li2O2. The reversible formation of Li2O 2 was successfully leveraged with the study of electro-catalysts and cathode materials for lithium-air batteries. The reversibility of Li 2O2 was thoroughly investigated using soft X-ray absorption spectroscopy and theoretical simulation, which substantiates the promise of using electrochromic films as electro-catalysts and/or cathode materials in lithium-air batteries.

  7. Oceanic nickel depletion and a methanogen famine before the Great Oxidation Event.

    PubMed

    Konhauser, Kurt O; Pecoits, Ernesto; Lalonde, Stefan V; Papineau, Dominic; Nisbet, Euan G; Barley, Mark E; Arndt, Nicholas T; Zahnle, Kevin; Kamber, Balz S

    2009-04-09

    It has been suggested that a decrease in atmospheric methane levels triggered the progressive rise of atmospheric oxygen, the so-called Great Oxidation Event, about 2.4 Gyr ago. Oxidative weathering of terrestrial sulphides, increased oceanic sulphate, and the ecological success of sulphate-reducing microorganisms over methanogens has been proposed as a possible cause for the methane collapse, but this explanation is difficult to reconcile with the rock record. Banded iron formations preserve a history of Precambrian oceanic elemental abundance and can provide insights into our understanding of early microbial life and its influence on the evolution of the Earth system. Here we report a decline in the molar nickel to iron ratio recorded in banded iron formations about 2.7 Gyr ago, which we attribute to a reduced flux of nickel to the oceans, a consequence of cooling upper-mantle temperatures and decreased eruption of nickel-rich ultramafic rocks at the time. We measured nickel partition coefficients between simulated Precambrian sea water and diverse iron hydroxides, and subsequently determined that dissolved nickel concentrations may have reached approximately 400 nM throughout much of the Archaean eon, but dropped below approximately 200 nM by 2.5 Gyr ago and to modern day values ( approximately 9 nM) by approximately 550 Myr ago. Nickel is a key metal cofactor in several enzymes of methanogens and we propose that its decline would have stifled their activity in the ancient oceans and disrupted the supply of biogenic methane. A decline in biogenic methane production therefore could have occurred before increasing environmental oxygenation and not necessarily be related to it. The enzymatic reliance of methanogens on a diminishing supply of volcanic nickel links mantle evolution to the redox state of the atmosphere.

  8. Hierarchical 3-dimensional nickel-iron nanosheet arrays on carbon fiber paper as a novel electrode for non-enzymatic glucose sensing.

    PubMed

    Kannan, Palanisamy; Maiyalagan, Thandavarayan; Marsili, Enrico; Ghosh, Srabanti; Niedziolka-Jönsson, Joanna; Jönsson-Niedziolka, Martin

    2016-01-14

    Three-dimensional nickel-iron (3-D/Ni-Fe) nanostructures are exciting candidates for various applications because they produce more reaction-active sites than 1-D and 2-D nanostructured materials and exhibit attractive optical, electrical and catalytic properties. In this work, freestanding 3-D/Ni-Fe interconnected hierarchical nanosheets, hierarchical nanospheres, and porous nanospheres are directly grown on a flexible carbon fiber paper (CFP) substrate by a single-step hydrothermal process. Among the nanostructures, 3-D/Ni-Fe interconnected hierarchical nanosheets show excellent electrochemical properties because of its high conductivity, large specific active surface area, and mesopores on its walls (vide infra). The 3-D/Ni-Fe hierarchical nanosheet array modified CFP substrate is further explored as a novel electrode for electrochemical non-enzymatic glucose sensor application. The 3-D/Ni-Fe hierarchical nanosheet arrays exhibit significant catalytic activity towards the electrochemical oxidation of glucose, as compared to the 3-D/Ni-Fe hierarchical nanospheres, and porous nanospheres. The 3-D/Ni-Fe hierarchical nanosheet arrays can access a large amount of glucose molecules on their surface (mesopore walls) for an efficient electrocatalytic oxidation process. Moreover, 3-D/Ni-Fe hierarchical nanosheet arrays showed higher sensitivity (7.90 μA μM(-1) cm(-2)) with wide linear glucose concentration ranging from 0.05 μM to 0.2 mM, and the low detection limit (LOD) of 0.031 μM (S/N = 3) is achieved by the amperometry method. Further, the 3-D/Ni-Fe hierarchical nanosheet array modified CFP electrode can be demonstrated to have excellent selectivity towards the detection of glucose in the presence of 500-fold excess of major important interferents. All these results indicate that 3-D/Ni-Fe hierarchical nanosheet arrays are promising candidates for non-enzymatic glucose sensing.

  9. Electroless deposition of electrodes in solid-oxide fuel cells

    SciTech Connect

    Murphy, M.M.; Van Herle, J.; McEvoy, A.J.; Thampi, K.R. . Inst. de Chimie Physique)

    1994-08-01

    This study demonstrates the use of electroless deposition for depositing anode and cathode electrocatalysts in solid-oxide fuel cells (SOFC). Ni, Pd, and Ag films produced by electroless deposition techniques were in intimate contact with the electrolyte yttria-stabilized zirconia, and were found to catalyze SOFC anodic and cathodic reactions. Power densities of such cells were in the range of 0.33 W/cm[sup 2] at 800 C. The operating life is low due to agglomeration of the anode and densification of the cathode. For intermediate temperature/range SOFCs electroless deposition is an alternative technique for electrode preparation, if long-term stability can be attained.

  10. Lithium metal oxide electrodes for lithium cells and batteries

    DOEpatents

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

    2004-01-13

    A lithium metal oxide positive electrode for a non-aqueous lithium cell is disclosed. The cell is prepared in its initial discharged state and has a general formula xLiMO.sub.2.(1-x)Li.sub.2 M'O.sub.3 in which 0

  11. Direct reform of graphite oxide electrodes by using ambient plasma for supercapacitor applications

    NASA Astrophysics Data System (ADS)

    Kim, Ho Jun; Jeong, Hae Kyung

    2017-10-01

    Ambient plasma is applied to graphite oxide electrodes directly to improve electrochemical properties for supercapacitor applications. Surface morphology of the electrodes after the plasma treatment changes dramatically and amount of oxygen reduced significantly, demonstrating a reduction effect on the graphite oxide electrode by the ambient plasma. Equivalent series resistance of the electrode also reduced from 108 Ω to 84 Ω after the plasma treatment. Corresponding specific capacitance, therefore, increases from 0.45 F cm-2 to 0.85 F cm-2, proving that the ambient plasma treatment is very efficient, clean, economic, and environment-friendly method to reform the graphite oxide electrodes directly for the supercapacitor applications.

  12. Oxidation of the pesticide atrazine at DSA electrodes.

    PubMed

    Malpass, G R P; Miwa, D W; Machado, S A S; Olivi, P; Motheo, A J

    2006-09-01

    This paper presents the study of the electrochemical oxidation of the pesticide atrazine at a Ti/Ru(0.3)Ti(0.7)O(2) dimensionally stable anodes (DSA). The effect of using different supporting electrolytes (NaCl, NaOH, NaNO(3), NaClO(4), H(2)SO(4) and Na(2)SO(4)) during the galvanostatic electrolysis of atrazine was investigated. It was observed that the removal of atrazine and total organic carbon (TOC) was only achieved at appreciable rates when NaCl was used as the supporting electrolyte, due to the oxidising species formed in this electrolyte (e.g. ClO(-)). Variation of the NaCl concentration demonstrated that, although only low concentrations of NaCl are necessary to result in the complete removal of atrazine in solution, TOC removal is almost linearly dependent on the quantity of NaCl in solution. Examination of the applied current density indicates that the efficiency of TOC removal reaches a maximum at 60 mA cm(-2). Testing of alternative electrode materials containing SnO(2) did not improve the efficiency of atrazine removal in Na(2)SO(4), but in NaCl a small increase was observed. Overall there appears to be no great advantage in using SnO(2)-containing electrodes over the Ti/Ru(0.3)Ti(0.7)O(2) electrode.

  13. Reductive-oxidation electrogenerated chemiluminescence (ECL) generation at a transparent silver nanowire electrode.

    PubMed

    Zhu, Yan; Hill, Caleb M; Pan, Shanlin

    2011-03-15

    We present the fabrication of a conductive, transparent electrode composed of Ag nanowires (NW) for spectroelectrochemical studies. Reductive-oxidation electrogenerated chemiluminescence (ECL) of Ru(bpy)3(2+) is generated at the Ag NW electrode in the presence of hydrogen peroxide and collected through the new transparent electrode. The ECL performance at the new nanostructured electrode is compared with several other electrodes, including bulk silver wire, glassy carbon disk, and thermally reduced transparent graphene oxide (tr-GO) electrodes. The Ag NW electrode is found to be the best electrode for the reductive-oxidation ECL generation because of its catalytic properties with respect to the reduction of hydrogen peroxide and its high surface area.

  14. Role of the oxide layer on Sn electrode in electrochemical reduction of CO2 to formate

    NASA Astrophysics Data System (ADS)

    Zhang, Rui; Lv, Weixin; Lei, Lixu

    2015-11-01

    The importance of oxide layer on Sn electrode to the efficiency of CO2 reduction has been evaluated by comparing the activities of Sn electrodes treated via etching and annealing. In KHCO3 aqueous solution saturated with CO2, Sn electrode with a native oxide layer exhibits high catalytic activity for CO2 reduction, in contrast, Sn electrode which is etched in HCl solution to remove the oxide layer or treated by annealing exhibits lower activity for CO2 reduction. If the etched Sn electrode is exposed in the air over 24 h, its catalytic performance for CO2 reduction will restore, meanwhile, the electrolysis current density for this electrode is around 1.5-fold than that for a untreated Sn electrode because the etching treatment makes the electrode rough and behave a larger superficial area.

  15. Vanadium nanobelts coated nickel foam 3D bifunctional electrode with excellent catalytic activity and stability for water electrolysis

    NASA Astrophysics Data System (ADS)

    Yu, Yu; Li, Pei; Wang, Xiaofang; Gao, Wenyu; Shen, Zongxu; Zhu, Yanan; Yang, Shuliang; Song, Weiguo; Ding, Kejian

    2016-05-01

    Pursuit of highly active, stable and low-cost electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is the key point for large-scale water splitting. A vanadium nanobelts coating on a nickel foam (V/NF) is proposed as an excellent 3D bifunctional electrode for water electrolysis here, which exhibits high activities with overpotentials of 292 and 176 mV at 10 mA cm-2 for OER and HER, respectively. When employed as a bifunctional electrocatalyst in an alkaline water electrolyzer, a cell voltage of 1.80 V was required to achieve 20 mA cm-2 with a slight increase during a 24 h durability test. The existence of the appropriate amount of nitrogen and oxygen elements in the surface region of vanadium nanobelts is regarded to be responsible for the electrocatalytic activity.Pursuit of highly active, stable and low-cost electrocatalysts for hydrogen evolution reaction (HER) and oxygen evolution reaction (OER) is the key point for large-scale water splitting. A vanadium nanobelts coating on a nickel foam (V/NF) is proposed as an excellent 3D bifunctional electrode for water electrolysis here, which exhibits high activities with overpotentials of 292 and 176 mV at 10 mA cm-2 for OER and HER, respectively. When employed as a bifunctional electrocatalyst in an alkaline water electrolyzer, a cell voltage of 1.80 V was required to achieve 20 mA cm-2 with a slight increase during a 24 h durability test. The existence of the appropriate amount of nitrogen and oxygen elements in the surface region of vanadium nanobelts is regarded to be responsible for the electrocatalytic activity. Electronic supplementary information (ESI) available: More SEM, TEM images, XRD patterns, LSV curves, XPS spectra. See DOI: 10.1039/c6nr02395a

  16. Probing and mapping electrode surfaces in solid oxide fuel cells.

    PubMed

    Blinn, Kevin S; Li, Xiaxi; Liu, Mingfei; Bottomley, Lawrence A; Liu, Meilin

    2012-09-20

    Solid oxide fuel cells (SOFCs) are potentially the most efficient and cost-effective solution to utilization of a wide variety of fuels beyond hydrogen (1-7). The performance of SOFCs and the rates of many chemical and energy transformation processes in energy storage and conversion devices in general are limited primarily by charge and mass transfer along electrode surfaces and across interfaces. Unfortunately, the mechanistic understanding of these processes is still lacking, due largely to the difficulty of characterizing these processes under in situ conditions. This knowledge gap is a chief obstacle to SOFC commercialization. The development of tools for probing and mapping surface chemistries relevant to electrode reactions is vital to unraveling the mechanisms of surface processes and to achieving rational design of new electrode materials for more efficient energy storage and conversion(2). Among the relatively few in situ surface analysis methods, Raman spectroscopy can be performed even with high temperatures and harsh atmospheres, making it ideal for characterizing chemical processes relevant to SOFC anode performance and degradation(8-12). It can also be used alongside electrochemical measurements, potentially allowing direct correlation of electrochemistry to surface chemistry in an operating cell. Proper in situ Raman mapping measurements would be useful for pin-pointing important anode reaction mechanisms because of its sensitivity to the relevant species, including anode performance degradation through carbon deposition(8, 10, 13, 14) ("coking") and sulfur poisoning(11, 15) and the manner in which surface modifications stave off this degradation(16). The current work demonstrates significant progress towards this capability. In addition, the family of scanning probe microscopy (SPM) techniques provides a special approach to interrogate the electrode surface with nanoscale resolution. Besides the surface topography that is routinely collected by AFM

  17. Probing and Mapping Electrode Surfaces in Solid Oxide Fuel Cells

    PubMed Central

    Blinn, Kevin S.; Li, Xiaxi; Liu, Mingfei; Bottomley, Lawrence A.; Liu, Meilin

    2012-01-01

    Solid oxide fuel cells (SOFCs) are potentially the most efficient and cost-effective solution to utilization of a wide variety of fuels beyond hydrogen 1-7. The performance of SOFCs and the rates of many chemical and energy transformation processes in energy storage and conversion devices in general are limited primarily by charge and mass transfer along electrode surfaces and across interfaces. Unfortunately, the mechanistic understanding of these processes is still lacking, due largely to the difficulty of characterizing these processes under in situ conditions. This knowledge gap is a chief obstacle to SOFC commercialization. The development of tools for probing and mapping surface chemistries relevant to electrode reactions is vital to unraveling the mechanisms of surface processes and to achieving rational design of new electrode materials for more efficient energy storage and conversion2. Among the relatively few in situ surface analysis methods, Raman spectroscopy can be performed even with high temperatures and harsh atmospheres, making it ideal for characterizing chemical processes relevant to SOFC anode performance and degradation8-12. It can also be used alongside electrochemical measurements, potentially allowing direct correlation of electrochemistry to surface chemistry in an operating cell. Proper in situ Raman mapping measurements would be useful for pin-pointing important anode reaction mechanisms because of its sensitivity to the relevant species, including anode performance degradation through carbon deposition8, 10, 13, 14 ("coking") and sulfur poisoning11, 15 and the manner in which surface modifications stave off this degradation16. The current work demonstrates significant progress towards this capability. In addition, the family of scanning probe microscopy (SPM) techniques provides a special approach to interrogate the electrode surface with nanoscale resolution. Besides the surface topography that is routinely collected by AFM and STM

  18. Hydrogen gas sensors based on electrostatically spray deposited nickel oxide thin film structures

    NASA Astrophysics Data System (ADS)

    Jamal, Raied K.; Aadim, Kadhim A.; Al-Zaidi, Qahtan G.; Taaban, Iman N.

    2015-09-01

    A simple, low-cost, and home-built electrostatic spray deposition (ESD) system with the stable cone-jet mode was used to deposit nickel oxide (NiO) thin films on glass substrates kept at temperature of 400 °C as the primary precursor solution of 0.1 M concentration hydrated nickel chloride was dissolved in isopropyl alcohol. Electrical measurements showed that these films were of n-type conductivity while their resistance response to hydrogen flow in air ambient was varied by 2.81% with the rise and recovery time of 48 s and 40 s, respectively.

  19. A Versatile Route for the Synthesis of Nickel Oxide Nanostructures Without Organics at Low Temperature

    PubMed Central

    2008-01-01

    Nickel oxide nanoparticles and nanoflowers have been synthesized by a soft reaction of nickel powder and water without organics at 100 °C. The mechanism for the formation of nanostructures is briefly described in accordance with decomposition of metal with water giving out hydrogen. The structure, morphology, and the crystalline phase of resulting nanostructures have been characterized by various techniques. Compared with other methods, the present method is simple, fast, economical, template-free, and without organics. In addition, the approach is nontoxic without producing hazardous waste and could be expanded to provide a general and convenient strategy for the synthesis of nanostructures to other functional nanomaterials.

  20. Synthesis and characterization of nickel oxide (NiO) thin films

    NASA Astrophysics Data System (ADS)

    Kate, R. S.; Khalate, S. A.; Deokate, R. J.

    2017-05-01

    Nickel Oxide (NiO) thin films were deposited by simple spray pyrolysis technique using nickel nitrate solution onto preheated glass substrate at substrate temperature 320 °C and 380 °C. Influence of substrate temperature on structural, morphological and optical properties were studied using X-ray diffraction, scanning electron microscopy and optical absorption. XRD results reveal that films are polycrystalline with single phase cubic structure and crystallinity of the film increases as the temperature increases. Surface morphological study shows spherical granular like shape at high deposition temperature. Optical band gap increases from 2.85 to 3.01 eV as the temperature increases.

  1. Practical nitric oxide measurement employing a nitric oxide-selective electrode

    NASA Astrophysics Data System (ADS)

    Ichimori, K.; Ishida, H.; Fukahori, M.; Nakazawa, H.; Murakami, E.

    1994-08-01

    An NO-selective electrode was developed as an easily applicable tool for a real-time nitric oxide (NO) measurement. The working electrode (0.2 mm diam) was made from Pt/Ir alloy coated with a three-layered membrane. The counterelectrode was made from a carbon fiber. When a stable NO donor, S-nitroso-N-acetyl-dl-penicillamine, was applied, the electrode current increased in a dose-dependent fashion. The current and calculated NO concentration showed a linear relationship in the range from 0.2 nM (S/N=1) to 1 μM of NO. The response of the electrode was 1.14±0.09 s. The effects of temperature, pH, and chemicals other than NO on the electrode current were also evaluated. Electrodes which were placed in the luminal side of rat aortic rings exhibited 30 pA of current due to NO generation induced by the addition of 10-6 M of acetylcholine. The current was eliminated in the presence of 50 μM NG-monomethyl-L-arginine, an inhibitor of NO synthase. Thus, this NO-selective electrode is applicable to real-time NO assay in biological systems.

  2. Submicron-Scale Heterogeneities in Nickel Sorption of Various Cell-Mineral Aggregates Formed by Fe(II)-Oxidizing Bacteria.

    PubMed

    Schmid, Gregor; Zeitvogel, Fabian; Hao, Likai; Ingino, Pablo; Adaktylou, Irini; Eickhoff, Merle; Obst, Martin

    2016-01-05

    Fe(II)-oxidizing bacteria form biogenic cell-mineral aggregates (CMAs) composed of microbial cells, extracellular organic compounds, and ferric iron minerals. CMAs are capable of immobilizing large quantities of heavy metals, such as nickel, via sorption processes. CMAs play an important role for the fate of heavy metals in the environment, particularly in systems characterized by elevated concentrations of dissolved metals, such as mine drainage or contaminated sediments. We applied scanning transmission (soft) X-ray microscopy (STXM) spectrotomography for detailed 3D chemical mapping of nickel sorbed to CMAs on the submicron scale. We analyzed different CMAs produced by phototrophic or nitrate-reducing microbial Fe(II) oxidation and, in addition, a twisted stalk structure obtained from an environmental biofilm. Nickel showed a heterogeneous distribution and was found to be preferentially sorbed to biogenically precipitated iron minerals such as Fe(III)-(oxyhydr)oxides and, to a minor extent, associated with organic compounds. Some distinct nickel accumulations were identified on the surfaces of CMAs. Additional information obtained from scatter plots and angular distance maps, showing variations in the nickel-iron and nickel-organic carbon ratios, also revealed a general correlation between nickel and iron. Although a high correlation between nickel and iron was observed in 2D maps, 3D maps revealed this to be partly due to projection artifacts. In summary, by combining different approaches for data analysis, we unambiguously showed the heterogeneous sorption behavior of nickel to CMAs.

  3. Effects of Oxide Layer Composition and Radial Compression on Nickel Release in Nitinol Stents

    NASA Astrophysics Data System (ADS)

    Sullivan, Stacey J. L.; Dreher, Maureen L.; Zheng, Jiwen; Chen, Lynn; Madamba, Daniel; Miyashiro, Katie; Trépanier, Christine; Nagaraja, Srinidhi

    2015-09-01

    There is a public health need to understand the effects of surface layer thickness and composition on corrosion in nickel-containing medical devices. To address this knowledge gap, five groups of Nitinol stents were manufactured by various processing methods that altered the titanium oxide layer. The following surfaces were created: >3500 nm thick mixed thermal oxide (OT), ~420 nm thick mixed thermal oxide (SP), ~130 nm thick mixed thermal oxide (AF), ~4 nm thick native oxide (MP), and an ~4 nm thick passivated oxide (EP). Radially compressed and not compressed devices were evaluated for nickel (Ni) ion release in a 60-day immersion test. The results indicated that OT stents released the most Ni, followed by stents in the SP and AF groups. For OT and SP stents, which exhibited the thickest oxide layers, radial compression significantly increased Ni release when compared to non-compressed stents. This result was not observed in AF, MP, SP stents indicating that the increased Ni release may be explained by cracking of the thicker oxide layers during crimping. Strong correlations were observed between oxide layer thickness and cumulative Ni release. These findings elucidate the importance of oxide layer thickness and composition on uniform corrosion of laser-cut Nitinol stents.

  4. The effect of different alkali metal hydroxides on nickel electrode life

    NASA Technical Reports Server (NTRS)

    Lim, H. S.; Verzwyvelt, S. A.; Clement, S. K.

    1988-01-01

    An accelerated cycle-life test (100-percent depth of discharge) of a sintered-type Ni electrode has been carried out in a flooded cell containing different alkali metal hydroxide electrolytes such as LiOH, NaOH, KOH, RbOH, and CsOH. Decrease in Ni electrode capacity with cycling was reduced as the radius of the alkali metal ions, with possible exception of CsOH.

  5. The effect of different alkali metal hydroxides on nickel electrode life

    NASA Technical Reports Server (NTRS)

    Lim, H. S.; Verzwyvelt, S. A.; Clement, S. K.

    1988-01-01

    An accelerated cycle-life test (100-percent depth of discharge) of a sintered-type Ni electrode has been carried out in a flooded cell containing different alkali metal hydroxide electrolytes such as LiOH, NaOH, KOH, RbOH, and CsOH. Decrease in Ni electrode capacity with cycling was reduced as the radius of the alkali metal ions, with possible exception of CsOH.

  6. Nickel supported on nitrogen-doped carbon nanotubes as hydrogen oxidation reaction catalyst in alkaline electrolyte

    DOE PAGES

    Zhuang, Zhongbin; Giles, Stephen A.; Zheng, Jie; ...

    2016-01-14

    The development of a low-cost, high-performance platinum-group-metal-free hydroxide exchange membrane fuel cell is hindered by the lack of a hydrogen oxidation reaction catalyst at the anode. Here we report that a composite catalyst, nickel nanoparticles supported on nitrogen-doped carbon nanotubes, has hydrogen oxidation activity similar to platinum-group metals in alkaline electrolyte. Although nitrogen-doped carbon nanotubes are a very poor hydrogen oxidation catalyst, as a support, it increases the catalytic performance of nickel nanoparticles by a factor of 33 (mass activity) or 21 (exchange current density) relative to unsupported nickel nanoparticles. Density functional theory calculations indicate that the nitrogen-doped support stabilizesmore » the nanoparticle against reconstruction, while nitrogen located at the edge of the nanoparticle tunes local adsorption sites by affecting the d-orbitals of nickel. Here, owing to its high activity and low cost, our catalyst shows significant potential for use in low-cost, high-performance fuel cells.« less

  7. Nickel supported on nitrogen-doped carbon nanotubes as hydrogen oxidation reaction catalyst in alkaline electrolyte

    SciTech Connect

    Zhuang, Zhongbin; Giles, Stephen A.; Zheng, Jie; Jenness, Glen R.; Caratzoulas, Stavros; Vlachos, Dionisios G.; Yan, Yushan

    2016-01-14

    The development of a low-cost, high-performance platinum-group-metal-free hydroxide exchange membrane fuel cell is hindered by the lack of a hydrogen oxidation reaction catalyst at the anode. Here we report that a composite catalyst, nickel nanoparticles supported on nitrogen-doped carbon nanotubes, has hydrogen oxidation activity similar to platinum-group metals in alkaline electrolyte. Although nitrogen-doped carbon nanotubes are a very poor hydrogen oxidation catalyst, as a support, it increases the catalytic performance of nickel nanoparticles by a factor of 33 (mass activity) or 21 (exchange current density) relative to unsupported nickel nanoparticles. Density functional theory calculations indicate that the nitrogen-doped support stabilizes the nanoparticle against reconstruction, while nitrogen located at the edge of the nanoparticle tunes local adsorption sites by affecting the d-orbitals of nickel. Here, owing to its high activity and low cost, our catalyst shows significant potential for use in low-cost, high-performance fuel cells.

  8. The decoration of multi-walled carbon nanotubes with nickel oxide nanoparticles using chemical method

    NASA Astrophysics Data System (ADS)

    Sahebian, S.; Zebarjad, S. M.; Vahdati Khaki, J.; Lazzeri, A.

    2016-07-01

    In this paper, nickel oxide (NiO) nanoparticles have been fabricated using wet method and deposited on the surface of multi-walled carbon nanotube (MWCNT). To do so, functional groups were introduced on the surface of MWCNTs by treating with concentrated nitric acid. Nickel oxide nanoparticles were formed on the surface of functionalized MWCNTs by incipient wetness impregnation of nickel nitrate, and the resultant product was calcinated in air atmosphere. Characteristics of the NiO/MWCNT were examined by various techniques, for example, Fourier transform spectroscopy (FTIR), X-ray diffraction analysis (XRD), transmission electron microscopy (TEM), thermogravimetric analyzer (TGA), and nitrogen adsorption-desorption isothermal as well as vibrating sample magnetometer (VSM). The FTIR spectra showed that carboxyl and hydroxyl functional groups existed on the surface of MWNTs after modification by concentrated nitric acid. The pattern of XRD indicated that MWNTs and nickel oxide nanoparticles coexisted in the NiO/MWCNT sample. The TEM images revealed that the NiO nanoparticles were distributed on the surface of the MWNTs, with the size ranging from 5 to 60 nm. Thermogravimetric analysis proved that NiO content decorated on MWCNTs was 80 and 15 wt%. The results of the Brunauer-Emmett-Teller (BET) data showed that the slight increment in the specific surface areas and porosities in the presence of the NiO nanoparticles on the surface of CNT.

  9. Nickel supported on nitrogen-doped carbon nanotubes as hydrogen oxidation reaction catalyst in alkaline electrolyte.

    PubMed

    Zhuang, Zhongbin; Giles, Stephen A; Zheng, Jie; Jenness, Glen R; Caratzoulas, Stavros; Vlachos, Dionisios G; Yan, Yushan

    2016-01-14

    The development of a low-cost, high-performance platinum-group-metal-free hydroxide exchange membrane fuel cell is hindered by the lack of a hydrogen oxidation reaction catalyst at the anode. Here we report that a composite catalyst, nickel nanoparticles supported on nitrogen-doped carbon nanotubes, has hydrogen oxidation activity similar to platinum-group metals in alkaline electrolyte. Although nitrogen-doped carbon nanotubes are a very poor hydrogen oxidation catalyst, as a support, it increases the catalytic performance of nickel nanoparticles by a factor of 33 (mass activity) or 21 (exchange current density) relative to unsupported nickel nanoparticles. Density functional theory calculations indicate that the nitrogen-doped support stabilizes the nanoparticle against reconstruction, while nitrogen located at the edge of the nanoparticle tunes local adsorption sites by affecting the d-orbitals of nickel. Owing to its high activity and low cost, our catalyst shows significant potential for use in low-cost, high-performance fuel cells.

  10. Extra and Intracellular Synthesis of Nickel Oxide Nanoparticles Mediated by Dead Fungal Biomass

    PubMed Central

    Salvadori, Marcia Regina; Ando, Rômulo Augusto; Oller Nascimento, Cláudio Augusto; Corrêa, Benedito

    2015-01-01

    The use of dead biomass of the fungus Hypocrea lixii as a biological system is a new, effective and environmentally friendly bioprocess for the production and uptake of nickel oxide nanoparticles (NPs), which has become a promising field in nanobiotechnology. Dead biomass of the fungus was successfully used to convert nickel ions into nickel oxide NPs in aqueous solution. These NPs accumulated intracellularly and extracellularly on the cell wall surface through biosorption. The average size, morphology and location of the NPs were characterized by transmission electron microscopy, high-resolution transmission electron microscopy, scanning electron microscopy, and energy dispersive X-ray spectroscopy. The NPs were mainly spherical and extra and intracellular NPs had an average size of 3.8 nm and 1.25 nm, respectively. X-ray photoelectron spectroscopy analysis confirmed the formation of nickel oxide NPs. Infrared spectroscopy detected the presence of functional amide groups, which are probable involved in particle binding to the biomass. The production of the NPs by dead biomass was analyzed by determining physicochemical parameters and equilibrium concentrations. The present study opens new perspectives for the biosynthesis of nanomaterials, which could become a potential biosorbent for the removal of toxic metals from polluted sites. PMID:26043111

  11. Nickel supported on nitrogen-doped carbon nanotubes as hydrogen oxidation reaction catalyst in alkaline electrolyte

    PubMed Central

    Zhuang, Zhongbin; Giles, Stephen A.; Zheng, Jie; Jenness, Glen R.; Caratzoulas, Stavros; Vlachos, Dionisios G.; Yan, Yushan

    2016-01-01

    The development of a low-cost, high-performance platinum-group-metal-free hydroxide exchange membrane fuel cell is hindered by the lack of a hydrogen oxidation reaction catalyst at the anode. Here we report that a composite catalyst, nickel nanoparticles supported on nitrogen-doped carbon nanotubes, has hydrogen oxidation activity similar to platinum-group metals in alkaline electrolyte. Although nitrogen-doped carbon nanotubes are a very poor hydrogen oxidation catalyst, as a support, it increases the catalytic performance of nickel nanoparticles by a factor of 33 (mass activity) or 21 (exchange current density) relative to unsupported nickel nanoparticles. Density functional theory calculations indicate that the nitrogen-doped support stabilizes the nanoparticle against reconstruction, while nitrogen located at the edge of the nanoparticle tunes local adsorption sites by affecting the d-orbitals of nickel. Owing to its high activity and low cost, our catalyst shows significant potential for use in low-cost, high-performance fuel cells. PMID:26762466

  12. Multifunctional Indium Tin Oxide Electrode Generated by Unusual Surface Modification

    PubMed Central

    Bouden, Sarra; Dahi, Antoine; Hauquier, Fanny; Randriamahazaka, Hyacinthe; Ghilane, Jalal

    2016-01-01

    The indium tin oxide (ITO) material has been widely used in various scientific fields and has been successfully implemented in several devices. Herein, the electrochemical reduction of ITO electrode in an organic electrolytic solution containing alkali metal, NaI, or redox molecule, N-(ferrocenylmethyl) imidazolium iodide, was investigated. The reduced ITO surfaces were investigated by X-ray photoelectron spectroscopy and grazing incident XRD demonstrating the presence of the electrolyte cation inside the material. Reversibility of this process after re-oxidation was evidenced by XPS. Using a redox molecule based ionic liquid as supporting electrolyte leads to fellow electrochemically the intercalation process. As a result, modified ITO containing ferrocenyl imidazolium was easily generated. This reduction process occurs at mild reducing potential around −1.8 V and causes for higher reducing potential a drastic morphological change accompanied with a decrease of the electrode conductivity at the macroscopic scale. Finally, the self-reducing power of the reduced ITO phase was used to initiate the spontaneous reduction of silver ions leading to the growth of Ag nanoparticles. As a result, transparent and multifunctional active ITO surfaces were generated bearing redox active molecules inside the material and Ag nanoparticles onto the surface. PMID:27857192

  13. Multifunctional Indium Tin Oxide Electrode Generated by Unusual Surface Modification

    NASA Astrophysics Data System (ADS)

    Bouden, Sarra; Dahi, Antoine; Hauquier, Fanny; Randriamahazaka, Hyacinthe; Ghilane, Jalal

    2016-11-01

    The indium tin oxide (ITO) material has been widely used in various scientific fields and has been successfully implemented in several devices. Herein, the electrochemical reduction of ITO electrode in an organic electrolytic solution containing alkali metal, NaI, or redox molecule, N-(ferrocenylmethyl) imidazolium iodide, was investigated. The reduced ITO surfaces were investigated by X-ray photoelectron spectroscopy and grazing incident XRD demonstrating the presence of the electrolyte cation inside the material. Reversibility of this process after re-oxidation was evidenced by XPS. Using a redox molecule based ionic liquid as supporting electrolyte leads to fellow electrochemically the intercalation process. As a result, modified ITO containing ferrocenyl imidazolium was easily generated. This reduction process occurs at mild reducing potential around ‑1.8 V and causes for higher reducing potential a drastic morphological change accompanied with a decrease of the electrode conductivity at the macroscopic scale. Finally, the self-reducing power of the reduced ITO phase was used to initiate the spontaneous reduction of silver ions leading to the growth of Ag nanoparticles. As a result, transparent and multifunctional active ITO surfaces were generated bearing redox active molecules inside the material and Ag nanoparticles onto the surface.

  14. Modified silver nanowire transparent electrodes with exceptional stability against oxidation

    NASA Astrophysics Data System (ADS)

    Idier, J.; Neri, W.; Labrugère, C.; Ly, I.; Poulin, P.; Backov, R.

    2016-03-01

    We report an easy method to prepare thin, flexible and transparent electrodes that show enhanced inertness toward oxidation using modified silver nanowires (Ag NWs). Stabilization is achieved through the adsorption of triphenylphosphine (PPh3) onto the Ag NW hybrid dispersions prior to their 2D organization as transparent electrodes on polyethylene terephtalate (PET) films. After 110 days in air (20 °C) under atmospheric conditions, the transmittance of the PET/Ag NW/PPh3 based films is nearly unchanged, while the transmittance of the PET/Ag NW-based films decreases by about 5%. The sheet resistance increases for both materials as time elapses, but the rate of increase is more than four times slower for films stabilized by PPh3. The improved transmittance and conductivity results in a significantly enhanced stability for the figure of merit σ dc/σ op. This phenomenon is highlighted in highly oxidative nitric acid vapor. The tested stabilized films in such conditions exhibit a decrease to σ dc/σ op of only 38% after 75 min, whereas conventional materials exhibit a relative loss of 71%. In addition, by contrast to other classes of stabilizers, such as polymer or graphene-based encapsulants, PPh3 does not alter the transparency or conductivity of the modified films. While the present films are made by membrane filtration, the stabilization method could be implemented directly in other liquid processes, including industrially scalable ones.

  15. Electrochemical oxidation of textile industry wastewater by graphite electrodes.

    PubMed

    Bhatnagar, Rajendra; Joshi, Himanshu; Mall, Indra D; Srivastava, Vimal C

    2014-01-01

    In the present article, studies have been performed on the electrochemical (EC) oxidation of actual textile industry wastewater by graphite electrodes. Multi-response optimization of four independent parameters namely initial pH (pHo): 4-10, current density (j): 27.78-138.89 A/m(2), NaCl concentration (w): 0-2 g/L and electrolysis time (t): 10-130 min have been performed using Box-Behnken (BB) experimental design. It was aimed to simultaneously maximize the chemical oxygen demand (COD) and color removal efficiencies and minimize specific energy consumption using desirability function approach. Pareto analysis of variance (ANOVA) showed a high coefficient of determination value for COD (R(2) = 0.8418), color (R(2) = 0.7010) and specific energy (R(2) = 0.9125) between the experimental values and the predicted values by a second-order regression model. Maximum COD and color removal and minimum specific energy consumed was 90.78%, 96.27% and 23.58 kWh/kg COD removed, respectively, were observed at optimum conditions. The wastewater, sludge and scum obtained after treatment at optimum condition have been characterized by various techniques. UV-visible study showed that all azo bonds of the dyes present in the wastewater were totally broken and most of the aromatic rings were mineralized during EC oxidation with graphite electrode. Carbon balance showed that out of the total carbon eroded from the graphite electrodes, 27-29.2% goes to the scum, 71.1-73.3% goes into the sludge and rest goes to the treated wastewater. Thermogravimetric analysis showed that the generated sludge and scum can be dried and used as a fuel in the boilers/incinerators.

  16. Nanostructured Metal Oxide Coatings for Electrochemical Energy Conversion and Storage Electrodes

    NASA Astrophysics Data System (ADS)

    Cordova, Isvar Abraxas

    The realization of an energy future based on safe, clean, sustainable, and economically viable technologies is one of the grand challenges facing modern society. Electrochemical energy technologies underpin the potential success of this effort to divert energy sources away from fossil fuels, whether one considers alternative energy conversion strategies through photoelectrochemical (PEC) production of chemical fuels or fuel cells run with sustainable hydrogen, or energy storage strategies, such as in batteries and supercapacitors. This dissertation builds on recent advances in nanomaterials design, synthesis, and characterization to develop novel electrodes that can electrochemically convert and store energy. Chapter 2 of this dissertation focuses on refining the properties of TiO2-based PEC water-splitting photoanodes used for the direct electrochemical conversion of solar energy into hydrogen fuel. The approach utilized atomic layer deposition (ALD); a growth process uniquely suited for the conformal and uniform deposition of thin films with angstrom-level thickness precision. ALD's thickness control enabled a better understanding of how the effects of nitrogen doping via NH3 annealing treatments, used to reduce TiO2's bandgap, can have a strong dependence on TiO2's thickness and crystalline quality. In addition, it was found that some of the negative effects on the PEC performance typically associated with N-doped TiO2 could be mitigated if the NH 3-annealing was directly preceded by an air-annealing step, especially for ultrathin (i.e., < 10 nm) TiO2 films. ALD was also used to conformally coat an ultraporous conductive fluorine-doped tin oxide nanoparticle (nanoFTO) scaffold with an ultrathin layer of TiO2. The integration of these ultrathin films and the oxide nanoparticles resulted in a heteronanostructure design with excellent PEC water oxidation photocurrents (0.7 mA/cm2 at 0 V vs. Ag/AgCl) and charge transfer efficiency. In Chapter 3, two innovative

  17. Monolithic Nickel (II) Oxide Aerogels Using an Organic Epoxide: The Importance of the Counter Ion

    SciTech Connect

    Gash, A E; Satcher, J H; Simpson, R L

    2004-01-13

    The synthesis and characterization of nickel (II) oxide aerogel materials prepared using the epoxide addition method is described. The addition of the organic epoxide propylene oxide to an ethanolic solution of NiCl{sub 2} 6H{sub 2}O resulted in the formation of an opaque light green monolithic gel and subsequent drying with supercritical CO{sub 2} gave a monolithic aerogel material of the same color. This material has been characterized using powder X-ray diffraction, electron microscopy, elemental analysis, and nitrogen adsorption/desorption analysis. The results indicate that the nickel (II) oxide aerogel has very low bulk density (98 kg/m{sup 3} ({approx}98 %porous)), high surface area (413 m{sup 2}/g), and has a particulate-type aerogel microstructure made up of very fine spherical particles with an open porous network. By comparison, a precipitate of Ni{sub 3}(NO{sub 3}){sub 2}(OH){sub 4} is obtained when the same preparation is attempted with the common Ni(NO{sub 3}){sub 2} 6H{sub 2}O salt as the precursor. The implications of the difference of reactivity of the two different precursors are discussed in the context of the mechanism of gel formation via the epoxide addition method. The synthesis of nickel (II) oxide aerogel, using the epoxide addition method, is especially unique in our experience. It is our first example of the successful preparation of a metal oxide aerogel using a metal divalent metal ion and may have implications for the application of this method to the preparation of aerogels or nanoparticles of other divalent metal oxides. To our knowledge this is the first report of a monolithic pure nickel (II) oxide aerogel materials.

  18. Mathematical modeling of electroless nickel deposition at steady state using rotating disk electrode

    SciTech Connect

    Kim, Y.S.; Sohn, H.J.

    1996-02-01

    Mathematical modeling of electroless nickel deposition was performed to predict the phosphorus content in Ni-P alloy film at steady state using the rotating disk system. The model consists of steady-state convective diffusion equations with nonlinear boundary conditions and overpotential equations satisfying the mixed potential theory. The weight percent of phosphorus predicted in Ni-P alloy agrees well with the experimental values within the experimental conditions carried out.

  19. Efficient reversible electrodes for solid oxide electrolyzer cells

    DOEpatents

    Elangovan, S.; Hartvigsen, Joseph J.; Zhao, Feng

    2013-01-15

    An electrolyzer cell is disclosed which includes a cathode to reduce an oxygen-containing molecule, such as H2O, CO.sub.2, or a combination thereof, to produce an oxygen ion and a fuel molecule, such as H.sub.2, CO, or a combination thereof. An electrolyte is coupled to the cathode to transport the oxygen ion to an anode. The anode is coupled to the electrolyte to receive the oxygen ion and produce oxygen gas therewith. In one embodiment, the anode may be fabricated to include an electron-conducting phase having a perovskite crystalline structure or structure similar thereto. This perovskite may have a chemical formula of substantially (Pr(.sub.1-x)La.sub.x)(z-y)A'.sub.yBO(3-.differential.), wherein 0nickel oxide intermixed with magnesium oxide.

  20. Efficient reversible electrodes for solid oxide electrolyzer cells

    DOEpatents

    Elangovan, Singaravelu; Hartvigsen, Joseph J.

    2011-07-12

    An electrolyzer cell is disclosed which includes a cathode to reduce an oxygen-containing molecule, such as H2O, CO2, or a combination thereof, to produce an oxygen ion and a fuel molecule, such as H2, CO, or a combination thereof. An electrolyte is coupled to the cathode to transport the oxygen ion to an anode. The anode is coupled to the electrolyte to receive the oxygen ion and produce oxygen gas therewith. In one embodiment, the anode may be fabricated to include an electron-conducting phase having a perovskite crystalline structure or structure similar thereto. This perovskite may have a chemical formula of substantially (Pr(1-x)Lax)(z-y)A'yBO(3-.differential.), wherein 0.ltoreq.x.ltoreq.0.5, 0.ltoreq.y.ltoreq.0.5, and 0.8.ltoreq.z.ltoreq.1.1. In another embodiment, the cathode includes an electron-conducting phase that contains nickel oxide intermixed with magnesium oxide.

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

    NASA Astrophysics Data System (ADS)

    Sundriyal, Poonam; Bhattacharya, Shantanu

    2017-03-01

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

  2. Hierarchically porous nickel oxide nanosheets grown on nickel foam prepared by one-step in situ anodization for high-performance supercapacitors.

    PubMed

    Yang, Li; Qian, Lei; Tian, Xianqing; Li, Jing; Dai, Jianyuan; Guo, Yong; Xiao, Dan

    2014-06-01

    Porous NiO nanosheets are successfully grown on nickel foam substrate through an in situ anodization by using molten KOH as the electrolyte. High-purity NiO is directly obtained by this one-step method without any subsequent treatment. The obtained NiO supported on nickel foam is used as a binder-free electrode for a supercapacitor and its pseudocapacitive behavior has been investigated by cyclic voltammetry and galvanostatic charge-discharge tests in a 6 M aqueous solution of KOH. Electrochemical data demonstrates that this binder-free electrode possesses ultrahigh capacitance (4.74 F cm(-2) at 4 mA cm(-2)), excellent rate capability, and cycling stability. After 1000 cycles, the areal capacitance value is 9.4 % lower than the initial value and maintains 85.4 % of the maximum capacitance value.

  3. Preparation and characterization of superparamagnetic nickel oxide particles by chemical route

    NASA Astrophysics Data System (ADS)

    Kalaie, Mohammad Reza; Youzbashi, Amir Ali; Meshkot, Mohammad Ali; Hosseini-Nasab, Farzad

    2016-08-01

    Homogeneous nickel oxide (NiO) nanoparticles with different sizes between 6 and 30 nm with narrow size distribution and low agglomeration were synthesized successfully by using different precipitated precursors and heat treatment under certain conditions. Powders were analyzed by different characterization methods. X-ray diffraction patterns revealed that the sizes of nanoparticles synthesized by nickel hydroxide and nickel oxalate precursors are under 10 nm, which are in good agreement with transition electron microscopy and field emission electron microscopy results. According to the vibrating sample magnetometer data, the NiO nanoparticles with sizes about 6 nm show superparamagnetic behavior. For superparamagnetic particles, the magnetization at maximum applied field of 20 kOe is 2.46 emu g-1.

  4. Bimetallic oxidative addition involving radical intermediates in nickel-catalyzed alkyl-alkyl Kumada coupling reactions.

    PubMed

    Breitenfeld, Jan; Ruiz, Jesus; Wodrich, Matthew D; Hu, Xile

    2013-08-14

    Many nickel-based catalysts have been reported for cross-coupling reactions of nonactivated alkyl halides. The mechanistic understanding of these reactions is still primitive. Here we report a mechanistic study of alkyl-alkyl Kumada coupling catalyzed by a preformed nickel(II) pincer complex ([(N2N)Ni-Cl]). The coupling proceeds through a radical process, involving two nickel centers for the oxidative addition of alkyl halide. The catalysis is second-order in Grignard reagent, first-order in catalyst, and zero-order in alkyl halide. A transient species, [(N2N)Ni-alkyl(2)](alkyl(2)-MgCl), is identified as the key intermediate responsible for the activation of alkyl halide, the formation of which is the turnover-determining step of the catalysis.

  5. Hydroxide Ion Oxidation in Aqueous Solutions Using Boron-Doped Diamond Electrodes.

    PubMed

    Irkham; Watanabe, Takeshi; Einaga, Yasuaki

    2017-07-05

    The electrochemical oxidation behavior of hydroxide ions at the surface of boron-doped diamond (BDD) electrodes is presented. The hydroxide ion oxidation behavior was found to be affected by the surface conditions of the BDD electrode. Over the NaOH concentration range of 0.5-10 mM, a well-defined voltammetric wave attributed to hydroxide ion oxidation was observed at ∼1.25 V versus a Ag/AgCl reference electrode when using an anodically oxidized BDD (AO-BDD) electrode, while it was observed at around ∼1.15 V when a cathodically reduced BDD (CR-BDD) electrode was used. Although the hydroxide ion oxidation profiles were slightly different for the AO-BDD and CR-BDD electrodes, the peak currents was each found to have linear relationships with the NaOH concentration over the same range.

  6. Electrochemical preparation of nickel and copper oxides-decorated graphene composite for simultaneous determination of dopamine, acetaminophen and tryptophan.

    PubMed

    Liu, Bingdi; Ouyang, Xiaoqian; Ding, Yaping; Luo, Liqing; Xu, Duo; Ning, Yanqun

    2016-01-01

    In the present work, transition metal oxides decorated graphene (GR) have been fabricated for simultaneous determination of dopamine (DA), acetaminophen (AC) and tryptophan (Trp) using square wave voltammetry. Electro-deposition is a facile preparation strategy for the synthesis of nickel oxide (NiO) and copper oxide (CuO) nanoparticles. GR can be modified by using citric acid to produce more functional groups, which is conducive to the deposition of dispersed metal particles. The morphologies and interface properties of the obtained NiO-CuO/GR nanocomposite were examined by scanning electron microscopy, energy dispersive X-ray spectroscopy and Raman spectroscopy. Moreover, the electrochemical performances of the composite film were investigated by cyclic voltammetry and electrochemical impedance spectroscopy. The modified electrode exhibited that the linear response ranges for detecting DA, AC and Trp were 0.5-20 μM, 4-400 μM and 0.3-40 μM, respectively, and the detection limits were 0.17 μM, 1.33 μM and 0.1 μM (S/N=3). Under optimal conditions, the sensor displayed high sensitivity, excellent stability and satisfactory results in real samples analysis.

  7. Vacancy-Induced Semiconductor-Insulator-Metal Transitions in Nonstoichiometric Nickel and Tungsten Oxides.

    PubMed

    Wang, Qi; Puntambekar, Ajinkya; Chakrapani, Vidhya

    2016-11-09

    Metal-insulator transitions in strongly correlated oxides induced by electrochemical charging have been attributed to formation of vacancy defects. However, the role of native defects in affecting these transitions is not clear. Here, we report a new type of phase transition in p-type, nonstoichiometric nickel oxide involving a semiconductor-to-insulator-to-metal transition along with the complete reversal of conductivity from p- to n-type at room temperature induced by electrochemical charging in a Li(+)-containing electrolyte. Direct observation of vacancy-ion interactions using in situ near-infrared photoluminescence spectroscopy show that the transition is a result of passivation of native nickel (cationic) vacancy defects and subsequent formation of oxygen (anionic) vacancy defects driven by Li(+) insertion into the lattice. Changes in the oxidation states of nickel due to defect interactions probed by X-ray photoemission spectroscopy support the above conclusions. In contrast, n-type, nonstoichiometric tungsten oxide shows only insulator-to-metal transition, which is a result of oxygen vacancy formation. The defect-property correlations shown here in these model systems can be extended to other oxides.

  8. Rapid synthesis of monodispersed highly porous spinel nickel cobaltite (NiCo{sub 2}O{sub 4}) electrode material for supercapacitors

    SciTech Connect

    Naveen, A. Nirmalesh Selladurai, S.

    2015-06-24

    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.

  9. Efficient Nickel Sulfide and Graphene Counter Electrodes Decorated with Silver Nanoparticles and Application in Dye-Sensitized Solar Cells

    NASA Astrophysics Data System (ADS)

    Yue, Gentian; Li, Fumin; Yang, Guang; Zhang, Weifeng

    2016-05-01

    We reported a facile two-step electrochemical-chemical approach for in situ growth of nickel sulfide and graphene counter electrode (CE) decorated with silver nanoparticles (signed NiS/Gr-Ag) and served in dye-sensitized solar cells (DSSCs). Under optimum conditions, the DSSC achieved a remarkable power conversion efficiency of 8.36 % assembled with the NiS/Gr-Ag CE, much higher than that based on the Pt CE (7.76 %). The surface morphology of NiS/Gr-Ag CE exhibited a smooth surface with cross-growth of NiS, graphene, and Ag nanoparticles, which was beneficial to the fast mass transport of electrolytes; increased the contact area of electrolytes and active materials; and enabled to speed up the reduction of triiodide to iodide. The research on the electrochemical properties also showed that the NiS/Gr-Ag CE possessed lower charge transfer resistance and more excellent electrocatalytic activity in iodide/triiodide electrolyte compared to the Pt electrode.

  10. Introduction of a carbon paste electrode based on nickel carbide for investigation of interaction between warfarin and vitamin K1.

    PubMed

    Torkashvand, Maryam; Gholivand, Mohammad Bagher; Taherpour, Avat Arman; Boochani, Arash; Akhtar, Arsalan

    2017-05-30

    In this paper a novel electrochemical sensor based on nickel carbide (Ni3C) nanoparticles as a new modifier was constructed. Ni3C nanoparticle was synthesized and characterized by scanning electron microscopy, X-ray diffraction and first-principles study. Electrochemical impedance spectroscopy (EIS) and cyclic voltammetry (CV) studies confirmed the electrode modification. Afterwards, the new electrode for the first time was used for interaction study between vitamin K1 and warfarin as an anticoagulant drug by differential pulse voltammetry. The adduct formation between the drug and vitamin K1 was improved by decreasing in anodic peak current of warfarin in the presence of different amounts of vitamin K1. The binding constant between warfarin and vitamin K1 was obtained by voltammetric and UV-vis and fluorescence spectroscopic methods. The molecular modeling method was also performed to explore the structural features and binding mechanism of warfarin to vitamin K1. The different aspects of modeling of vitamin K1 and warfarin and their adduct structures confirmed the adduct formation by hydrogen bonding. Copyright © 2017 Elsevier B.V. All rights reserved.

  11. Counter electrodes from polymorphic platinum-nickel hollow alloys for high-efficiency dye-sensitized solar cells

    NASA Astrophysics Data System (ADS)

    Wang, Jing; Tang, Qunwei; He, Benlin; Yang, Peizhi

    2016-10-01

    Precious platinum counter electrode (CE) has been an economic burden for future commercialization of dye-sensitized solar cells (DSSCs). Low-platinum alloy CE catalysts are promising in bringing down the solar cell cost without reducing photovoltaic performances. We present here a facile strategy of fabricating ZnO nanorods assisted platinum-nickel (PtNi) alloy microtube CEs for liquid-junction DSSCs. By adjusting the concentration of zinc precursors, the ZnO nanostructures and therefore PtNi alloys are optimized to maximize the electrocatalytic behaviors toward triiodide reduction reaction. The maximal power conversion efficiency is determined as high as 8.43% for liquid-junction DSSC device with alloyed PtNi microtube CE synthesized at 75 mM Zn(NO3)2 aqueous solution, yielding a 32.8% enhancement in cell efficiency in comparison with the solar cell from pristine platinum electrode. Moreover, the dissolution resistance and charge-transfer ability toward redox couples have also been markedly enhanced due to competitive dissolution reactions and alloyed effects.

  12. Controllable preparation of nanoporous Ni3S2 films by sulfuration of nickel foam as promising asymmetric supercapacitor electrodes

    NASA Astrophysics Data System (ADS)

    Li, Jin; Wang, Shulin; Xiao, Ting; Tan, Xinyu; Xiang, Peng; Jiang, Lihua; Deng, Can; Li, Wei; Li, Mingming

    2017-10-01

    In this work, we reported a controllable preparation of nanoporous Ni3S2 films by a simple solvothermal-assisted sulfuration of nickel foam. The pore size can be easily adjusted by controlling the sulfuration time. Electrochemical tests show that the specific capacitance and the cycling performance of the Ni3S2 films were sensitive to their pore size. The Ni3S2 films with optimal pore size demonstrate a high specific capacitance (3.42 F/cm2 at 1 mA/cm2) and excellent cycling stability (about 102% after 4250 cycles at 7.5 mA/cm2). By contrast, the Ni3S2 films with either too large or too small pore size show much lower capacitance and relatively worse cycling stability. An asymmetric supercapacitor by using the optimal Ni3S2 film as the positive electrode and activated carbon coated on Ni foam as the negative electrode was also successfully assembled, which exhibited a superior energy density of 41.8 Wh/kg at power density of 155 W/kg and a high capacitance retention of 76.6% after 2000 cycles.

  13. Transient current response of iron-nickel-chromium alloy rotating cylindrical electrodes scribed with a dropped stylus

    SciTech Connect

    Odegard, C.A.; Bronson, A.

    1997-10-01

    The scribing technique was used to investigate dissolution and repassivation kinetics of three iron-nickel-chromium (Fe-Ni-Cr) electrodes immersed in a 0.01 M potassium chloride (KCl) + 0.01 M sulfuric acid (H{sub 2}SO{sub 4}) electrolyte. The study related the extent of surface deformation with the electrochemical response, as a result of a Vickers diamond impacting a rotating cylindrical electrode (RCE). The transient current response and transient impact force (F{sub imp}) of the stylus were measured simultaneously. For a given alloy, the scratch current density (i{sub s}) was observed to remain unchanged with respect to F{sub imp} of the stylus from 44 N to 432 N. Activation charge density (q{sub act}) was observed to remain constant with F{sub imp}, whereas the repassivation charge density (q{sub rep}) increased with increasing F{sub imp}. Surface deformation of the alloys was discussed according to the principles of microindentation of alloys, which showed that electrochemical responses for the alloys corresponded with the plastically deformed zone associated with the scratch. Alloy composition affected i{sub s}, q{sub act}, and q{sub rep} for the F{sub imp} values measured.

  14. A novel asymmetric supercapacitors based on binder-free carbon fiber paper@ nickel cobaltite nanowires and graphene foam electrodes

    NASA Astrophysics Data System (ADS)

    Tang, Qianqiu; Chen, Mingming; Wang, Le; Wang, Gengchao

    2015-01-01

    Aqueous-based asymmetric supercapacitors (AASCs) provide an effective way to improve the energy density of the device by broadening the operating voltage window. In this work, nickel cobaltite (NiCo2O4) nanowires are grown homogenously on carbon fiber paper (CFP) to obtain a binder-free CFP@NiCo2O4 positive electrode through a simple hydrothermal method followed by calcination. The highly porous graphene foam (GF) as negative electrode which also exhibits self-supporting structure is prepared by a facile mild reduction process. Taking advantages of the complementary voltage window of CFP@NiCo2O4 and GF, the as-fabricated CFP@NiCo2O4//GF AASC obtains a stable working voltage window of 1.6 V, and a high energy density of 34.5 Wh kg-1 at the power density of 547 W kg-1, which still maintains 17.1 Wh kg-1 at 9.68 kW kg-1. Furthermore, it exhibits superior cycling performance with 92.2% capacitance retention rate after 10000 cycles.

  15. Synthesis and Stability of a Nanoparticle-Infiltrated Solid OxideFuel Cell Electrode

    SciTech Connect

    Sholklapper, Tal Z.; Radmilovic, Velimir; Jacobson, Craig P.; Visco, Steven J.; De Jonghe, Lutgard C.

    2006-11-20

    Nanoparticulate catalysts infiltrated into SOFC (Solid OxideFUel Cell) electrodes can significantly enhance the cell performance, butthe stability of these electrodes has been an open issue. An infiltrationprocedure is reported that leads to a stable scandia-stablized zirconia(SSZ) cathode electrode performance.

  16. Impedances of electrochemically impregnated nickel electrodes as functions of potential, KOH concentration, and impregnation method

    NASA Technical Reports Server (NTRS)

    Reid, Margaret A.

    1989-01-01

    Impedances of fifteen electrodes form each of the four U.S. manufactures were measured at 0.200 V vs. the Hg/HgO reference electrode. This corresponds to a voltage of 1.145 for a Ni/H2 cell. Measurements were also made of a representative sample of these at 0.44 V. At the higher voltage, the impedances were small and very similar, but at the lower voltage there were major differences between manufacturers. Electrodes from the same manufacturers showed only small differences. The impedances of electrodes from two manufacturers were considerably different in 26 percent KOH from those in 31 percent KOH. These preliminary results seen to correlate with the limited data from earlier life testing of cells from these manufacturers. The impedances of cells being tested for Space Station Freedom are being followed, and more impendance measurements of electrodes are being performed as functions of manufacturer, voltage, electrolyte concentration, and cycle history in hopes of finding better correlations of impedance with life.

  17. A Facile Method to In-Situ Synthesize Porous Ni₂GeO₄ Nano-Sheets on Nickel Foam as Advanced Anode Electrodes for Li-Ion Batteries.

    PubMed

    Ma, Delong; Shi, Xiaomin; Hu, Anming

    2016-11-19

    A strategy for growth of porous Ni₂GeO₄ nanosheets on conductive nickel (Ni) foam with robust adhesion as a high-performance electrode for Li-ion batteries is proposed and realized, through a facile two-step method. It involves the low temperature hydro-thermal synthesis of bimetallic (Ni, Ge) hydroxide nanosheets precursor on Ni foam substrates and subsequent thermal transformation to porous Ni₂GeO₄ nanosheets. The as-prepared Ni₂GeO₄ nanosheets possess many interparticle mesopores with a size range from 5 to 15 nm. The hierarchical structure of porous Ni₂GeO₄ nanosheets supported by Ni foam promises fast electron and ion transport, large electroactive surface area, and excellent structural stability. The efficacy of the specially designed structure is demonstrated by the superior electrochemical performance of the generated Ni₂GeO₄ nanosheets including a high capacity of 1.8 mA·h·cm(-2) at a current density of 50 μA·cm(-2), good cycle stability, and high power capability at room temperature. Because of simple conditions, this fabrication strategy may be easily extended to other mixed metal oxides (MxGeOy).

  18. Pathological features of different sizes of nickel oxide following intratracheal instillation in rats.

    PubMed

    Ogami, Akira; Morimoto, Yasuo; Myojo, Toshihiko; Oyabu, Takako; Murakami, Masahiro; Todoroki, Motoi; Nishi, Kenichiro; Kadoya, Chikara; Yamamoto, Makoto; Tanaka, Isamu

    2009-08-01

    Focusing on the "size" impact of particles, the objective of this study was to analyze morphological and qualitative changes over time in the development of inflammation and collagen deposition in lung tissue after intratracheal instillation of two sizes of nickel oxide in rats, in comparison with the results of instillation of crystalline silica and titanium dioxide. The fine-sized nickel oxide sample (nNiOm: median diameter of agglomerated particles 0.8 microm) was prepared from crude particles of nickel oxide (median diameter of primary particle 27 nm) by liquid-phase separation. Another samples of micrometer-sized nickel oxide (NiO: median diameter of particles 4.8 microm), crystalline silica (Min-U-SIL-5; geometric mean diameter 1.6 microm, geometric standard deviation [GSD] 2.0), and TiO(2) (geometric mean diameter 1.5 microm, GSD 1.8) were also used. Well-sonicated samples of 2 mg per 0.4 ml saline or saline alone (control) were intratracheally instilled into Wistar rats (males, 10 wk old). Bronchoalveolar lavage fluid (BAL)F and lung tissue were examined at 3 days, 1 wk, 1 mo, 3 mo, and 6 mo after instillation, from 5 rats of each group. Histopathological findings showed that the infiltration of macrophages or polymorphonuclear cells and the alveolitis in rats treated with nNiOm were remarkable over time and similar to the effects of crystalline silica. The numbers of total cells in BALF and the percentage of plymorphonuclear leukocytes (PMNs) also increased in the nNiOm group and silica group. The point counting method (PCM) showed a significant increase of inflammatory area, with the peak at 3 mo after instillation in the nNiOm group. In contrast, NiO treatment showed only a slight inflammatory change. Collagen deposition in two regions in the lung tissue (alveolar duct and pleura) showed an increasing collagen deposition rate in nNiOm at 6 mo. Our results suggest that submicrometer nano-nickel oxide is associated with greater toxicity, as for crystalline

  19. Pt/Co/oxide and oxide/Co/Pt electrodes for perpendicular magnetic tunnel junctions

    NASA Astrophysics Data System (ADS)

    Nistor, L. E.; Rodmacq, B.; Auffret, S.; Dieny, B.

    2009-01-01

    This letter presents a study of perpendicular magnetic anisotropy in oxide/Co/Pt structures, which could constitute the upper magnetic electrode of magnetic tunnel junctions. The growth of cobalt layers on SiO2 substrates shows that all 0.6 nm thick Co films are superparamagnetic, whereas perpendicular magnetic anisotropy is obtained for 1.5 nm films after annealing. Co layers grown on various Al and Mg oxides prepared by sputtering also exhibit perpendicular magnetic anisotropy after annealing. Combined with inverse Pt/Co(CoFeB)/oxide stackings, these structures allow preparing tunnel junctions with thicker magnetic electrodes and much better thermal stability than those based on standard Pt/Co multilayers.

  20. Anodic oxidation with doped diamond electrodes: a new advanced oxidation process.

    PubMed

    Kraft, Alexander; Stadelmann, Manuela; Blaschke, Manfred

    2003-10-31

    Boron-doped diamond anodes allow to directly produce OH* radicals from water electrolysis with very high current efficiencies. This has been explained by the very high overvoltage for oxygen production and many other anodic electrode processes on diamond anodes. Additionally, the boron-doped diamond electrodes exhibit a high mechanical and chemical stability. Anodic oxidation with diamond anodes is a new advanced oxidation process (AOP) with many advantages compared to other known chemical and photochemical AOPs. The present work reports on the use of diamond anodes for the chemical oxygen demand (COD) removal from several industrial wastewaters and from two synthetic wastewaters with malic acid and ethylenediaminetetraacetic (EDTA) acid. Current efficiencies for the COD removal between 85 and 100% have been found. The formation and subsequent removal of by-products of the COD oxidation has been investigated for the first time. Economical considerations of this new AOP are included.