WorldWideScience

Sample records for based electrolytic reduction

  1. Observations of Oxygen Ion Behavior in the Lithium-Based Electrolytic Reduction of Uranium Oxide

    Energy Technology Data Exchange (ETDEWEB)

    Steven D. Herrmann; Shelly X. Li; Brenda E. Serrano-Rodriguez

    2009-09-01

    Parametric studies were performed on a lithium-based electrolytic reduction process at bench-scale to investigate the behavior of oxygen ions in the reduction of uranium oxide for various electrochemical cell configurations. Specifically, a series of eight electrolytic reduction runs was performed in a common salt bath of LiCl – 1 wt% Li2O. The variable parameters included fuel basket containment material (i.e., stainless steel wire mesh and sintered stainless steel) and applied electrical charge (i.e., 75 – 150% of the theoretical charge for complete reduction of uranium oxide in a basket to uranium metal). Samples of the molten salt electrolyte were taken at regular intervals throughout each run and analyzed to produce a time plot of Li2O concentrations in the bulk salt over the course of the runs. Following each run, the fuel basket was sectioned and the fuel was removed. Samples of the fuel were analyzed for the extent of uranium oxide reduction to metal and for the concentration of salt constituents, i.e., LiCl and Li2O. Extents of uranium oxide reduction ranged from 43 – 70% in stainless steel wire mesh baskets and 8 – 33 % in sintered stainless steel baskets. The concentrations of Li2O in the salt phase of the fuel product from the stainless steel wire mesh baskets ranged from 6.2 – 9.2 wt%, while those for the sintered stainless steel baskets ranged from 26 – 46 wt%. Another series of tests was performed to investigate the dissolution of Li2O in LiCl at 650 °C across various cathode containment materials (i.e., stainless steel wire mesh, sintered stainless steel and porous magnesia) and configurations (i.e., stationary and rotating cylindrical baskets). Dissolution of identical loadings of Li2O particulate reached equilibrium within one hour for stationary stainless steel wire mesh baskets, while the same took several hours for sintered stainless steel and porous magnesia baskets. Rotation of an annular cylindrical basket of stainless steel

  2. Observations of Oxygen Ion Behavior in the Lithium-Based Electrolytic Reduction of Uranium Oxide

    International Nuclear Information System (INIS)

    Parametric studies were performed on a lithium-based electrolytic reduction process at bench-scale to investigate the behavior of oxygen ions in the reduction of uranium oxide for various electrochemical cell configurations. Specifically, a series of eight electrolytic reduction runs was performed in a common salt bath of LiCl - 1 wt% Li2O. The variable parameters included fuel basket containment material (i.e., stainless steel wire mesh and sintered stainless steel) and applied electrical charge (i.e., 75 - 150% of the theoretical charge for complete reduction of uranium oxide in a basket to uranium metal). Samples of the molten salt electrolyte were taken at regular intervals throughout each run and analyzed to produce a time plot of Li2O concentrations in the bulk salt over the course of the runs. Following each run, the fuel basket was sectioned and the fuel was removed. Samples of the fuel were analyzed for the extent of uranium oxide reduction to metal and for the concentration of salt constituents, i.e., LiCl and Li2O. Extents of uranium oxide reduction ranged from 43-70% in stainless steel wire mesh baskets and 8-33% in sintered stainless steel baskets. The concentrations of Li2O in the salt phase of the fuel product from the stainless steel wire mesh baskets ranged from 6.2-9.2 wt%, while those for the sintered stainless steel baskets ranged from 26-46 wt%. Another series of tests was performed to investigate the dissolution of Li2O in LiCl at 650 C across various cathode containment materials (i.e., stainless steel wire mesh, sintered stainless steel and porous magnesia) and configurations (i.e., stationary and rotating cylindrical baskets). Dissolution of identical loadings of Li2O particulate reached equilibrium within one hour for stationary stainless steel wire mesh baskets, while the same took several hours for sintered stainless steel and porous magnesia baskets. Rotation of an annular cylindrical basket of stainless steel wire mesh accelerated the

  3. Observations of Oxygen Ion Behavior in the Lithium- Based Electrolytic Reduction of Uranium Oxide

    Energy Technology Data Exchange (ETDEWEB)

    Herrmann, S.D.; Li, S.X.; Serrano-Rodriguez, B.E. [Idaho National Laboratory, P.O. Box 1625, Idaho Falls, Idaho 83415 (United States)

    2009-06-15

    Development of a lithium-based electrolytic reduction process to convert oxide fuel to metal is being pursued by various researchers to facilitate subsequent pyro-processing of the metalized fuel product. In such pursuits, uranium oxide particles are contacted by an electrically conductive material and immersed in a pool of LiCl-Li{sub 2}O at 650 deg. C. A controlled current is passed between the fuel particles (as the cathode) and a suitable anode to reduce the uranium oxide to metal at the cathode and to oxidize oxygen ions to gas at the anode. In this process, the effective liberation and transport of oxygen ions from the oxide fuel particles within a cathode structure to the anode is paramount to the viability of this process. Parametric studies were performed on a lithium-based electrolytic reduction process at bench-scale in an inert atmosphere glovebox to investigate the behavior of oxygen ions in the reduction of uranium oxide for various electrochemical cell configurations. Specifically, a series of eight electrolytic reduction runs in a common salt bath of LiCl - 1 wt% Li{sub 2}O was performed with varying applied charges (75 - 150% of theoretical) and fuel basket containment materials (stainless steel wire mesh and sintered stainless steel). Samples of the molten salt electrolyte were taken at regular intervals throughout each run and analyzed to produce a time plot of Li{sub 2}O concentrations in the bulk salt over the course of the runs. Following each run, the fuel basket was sectioned and the fuel was removed. Samples of the fuel were analyzed for the extent of uranium oxide reduction to metal and for the concentration of salt constituents, i.e., LiCl and Li{sub 2}O. Extents of uranium oxide reduction ranged from 35 - 70% in stainless steel wire mesh baskets and 8 - 33 % in sintered stainless steel baskets. The concentrations of Li{sub 2}O in the salt phase of the fuel product from the stainless steel wire mesh baskets ranged from 6.2 to 9.3%, while

  4. F4U production by electrolytic reduction

    International Nuclear Information System (INIS)

    As a part of the nuclear fuel cycle program developed at the Spanish Atomic Energy Commission it has been studied the electrolytic reduction of U-VI to U-IV. The effect of the materials, electrolyte concentration, pH, current density, cell size and laboratory scale production is studied. The Pilot Plant and the production data are also described. (Author) 18 refs

  5. Safeguard monitoring of direct electrolytic reduction

    Science.gov (United States)

    Jurovitzki, Abraham L.

    Nuclear power is regaining global prominence as a sustainable energy source as the world faces the consequences of depending on limited fossil based, CO2 emitting fuels. A key component to achieving this sustainability is to implement a closed nuclear fuel cycle. Without achieving this goal, a relatively small fraction of the energy value in nuclear fuel is actually utilized. This involves recycling of spent nuclear fuel (SNF)---separating fissile actinides from waste products and using them to fabricate fresh fuel. Pyroprocessing is a viable option being developed for this purpose with a host of benefits compared to other recycling options, such as PUREX. Notably, pyroprocessing is ill suited to separate pure plutonium from spent fuel and thus has non-proliferation benefits. Pyroprocessing involves high temperature electrochemical and chemical processing of SNF in a molten salt electrolyte. During this batch process, several intermediate and final streams are produced that contain radioactive material. While pyroprocessing is ineffective at separating pure plutonium, there are various process misuse scenarios that could result in diversion of impure plutonium into one or more of these streams. This is a proliferation risk that should be addressed with innovative safeguards technology. One approach to meeting this challenge is to develop real time monitoring techniques that can be implemented in the hot cells and coupled with the various unit operations involved with pyroprocessing. Current state of the art monitoring techniques involve external chemical assaying which requires sample removal from these unit operations. These methods do not meet International Atomic Energy Agency's (IAEA) timeliness requirements. In this work, a number of monitoring techniques were assessed for their viability as online monitoring tools. A hypothetical diversion scenario for the direct electrolytic reduction process was experimentally verified (using Nd2O3 as a surrogate for PuO2

  6. Nitrogen-modified carbon-based catalysts for oxygen reduction reaction in polymer electrolyte membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Subramanian, Nalini P.; Li, Xuguang; Nallathambi, Vijayadurda; Kumaraguru, Swaminatha P.; Colon-Mercado, Hector; Wu, Gang; Lee, Jong-Won; Popov, Branko N. [Center for Electrochemical Engineering, Department of Chemical Engineering, University of South Carolina, Columbia, SC 29208 (United States)

    2009-03-01

    Nitrogen-modified carbon-based catalysts for oxygen reduction were synthesized by modifying carbon black with nitrogen-containing organic precursors. The electrocatalytic properties of catalysts were studied as a function of surface pre-treatments, nitrogen and oxygen concentrations, and heat-treatment temperatures. On the optimum catalyst, the onset potential for oxygen reduction is approximately 0.76 V (NHE) and the amount of hydrogen peroxide produced at 0.5 V (NHE) is approximately 3% under our experimental conditions. The characterization studies indicated that pyridinic and graphitic (quaternary) nitrogens may act as active sites of catalysts for oxygen reduction reaction. In particular, pyridinic nitrogen, which possesses one lone pair of electrons in addition to the one electron donated to the conjugated {pi} bond, facilitates the reductive oxygen adsorption. (author)

  7. Alternative Anodes for the Electrolytic Reduction of Uranium Dioxide

    Science.gov (United States)

    Merwin, Augustus

    Reprocessing of spent nuclear fuel is an essential step in closing the nuclear fuel cycle. In order to consume current stockpiles, ceramic uranium dioxide spent nuclear fuel will be subjected to an electrolytic reduction process. The current reduction process employs a platinum anode and a stainless steel alloy 316 cathode in a molten salt bath consisting of LiCl-2wt% Li 2O and occurs at 700°C. A major shortcoming of the existing process is the degradation of the platinum anode under the severely oxidizing conditions encountered during electrolytic reduction. This work investigates alternative anode materials for the electrolytic reduction of uranium oxide. The high temperature and extreme oxidizing conditions encountered in these studies necessitated a unique set of design constraints on the system. Thus, a customized experimental apparatus was designed and constructed. The electrochemical experiments were performed in an electrochemical reactor placed inside a furnace. This entire setup was housed inside a glove box, in order to maintain an inert atmosphere. This study investigates alternative anode materials through accelerated corrosion testing. Surface morphology was studied using scanning electron microscopy. Surface chemistry was characterized using energy dispersive spectroscopy and Raman spectroscopy. Electrochemical behavior of candidate materials was evaluated using potentiodynamic polarization characteristics. After narrowing the number of candidate electrode materials, ferrous stainless steel alloy 316, nickel based Inconel 718 and elemental tungsten were chosen for further investigation. Of these materials only tungsten was found to be sufficiently stable at the anodic potential required for electrolysis of uranium dioxide in molten salt. The tungsten anode and stainless steel alloy 316 cathode electrode system was studied at the required reduction potential for UO2 with varying lithium oxide concentrations. Electrochemical impedance spectroscopy

  8. Numerical simulation on electrolyte flow field in 156 kA drained aluminum reduction cells

    Institute of Scientific and Technical Information of China (English)

    ZHOU Nai-jun; XIA xiao-xia; WANG Fu-qiang

    2007-01-01

    Based on the commercial CFD software CFX-4.3, two-phase flow of electrolyte in 156 kA drained aluminum reduction cells with a new structure was numerically simulated by multi-fluid model and k-εturbulence model. The results show that the electrolyte flow in the drained cells is more even than in the conventional cells. Corresponding to center point feeding,the electrolyte flow in the drained cells is more advantageous to the release of anode gas, the dissolution and diflusion of alumina, and the gradient reduction of the electrolyte density and temperature. The average velocity of the electrolyte is 8.3 cm/s, and the maximum velocity is 59.5 cm/s.The average and maximum velocities of the gas are 23.2 cm/s and 61.1 cm/s, respectively. The cathode drained slope and anode cathode distance have certain effects on the electrolyte flow.

  9. Alternate Anodes for the Electrolytic Reduction of UO2

    Science.gov (United States)

    Merwin, Augustus; Chidambaram, Dev

    2015-01-01

    The electrolytic reduction process of UO2 employs a platinum anode and a stainless steel cathode in molten LiCl-LiO2 maintained at 973 K (700 °C). The degradation of platinum under the severely oxidizing conditions encountered during the process is an issue of concern. In this study, Inconel 600 and 718, stainless steel alloy 316, tungsten, nickel, molybdenum, and titanium, were investigated though electrochemical polarization techniques, electron microscopy, Raman spectroscopy, and X-ray photoelectron spectroscopy to serve as potential anode materials. Of the various materials investigated, only tungsten exhibited sufficient stability at the required potential in the molten electrolyte. Tungsten anodes were further studied in molten LiCl-LiO2 electrolyte containing 2, 4, and 6 wt pct of Li2O. In LiCl-2 wt pct Li2O tungsten was found to be sufficiently stable to both oxidation and microstructural changes and the stability is attributed to the formation of a lithium-intercalated tungsten oxide surface film. Increase in the concentration of Li2O was found to lead to accelerated corrosion of the anode, in conjunction with the formation of a peroxotungstate oxide film.

  10. Study on electrolytic reduction with controlled oxygen flow for iron from molten oxide slag containing FeO

    Directory of Open Access Journals (Sweden)

    Gao Y.M.

    2013-01-01

    Full Text Available A ZrO2-based solid membrane electrolytic cell with controlled oxygen flow was constructed: graphite rod /[O]Fe+C saturated / ZrO2(MgO/(FeO slag/iron crucible. The feasibility of extraction of iron from molten oxide slag containing FeO at an applied voltage was investigated by means of the electrolytic cell. The effects of some important process factors on the FeO electrolytic reduction with the controlled oxygen flow were discussed. The results show that: solid iron can be extracted from molten oxide slag containing FeO at 1450ºC and an applied potential of 4V. These factors, such as precipitation and growth of solid iron dendrites, change of the cathode active area on the inner wall of the iron crucible and ion diffusion flux in the molten slag may affect the electrochemical reaction rate. The reduction for Fe2+ ions mainly appears on new iron dendrites of the iron crucible cathode, and a very small amount of iron are also formed on the MSZ (2.18% MgO partially stabilized zirconia tube/slag interface due to electronic conductance of MSZ tube. Internal electronic current through MSZ tube may change direction at earlier and later electrolytic reduction stage. It has a role of promoting electrolytic reduction for FeO in the molten slag at the earlier stage, but will lower the current efficiency at the later stage. The final reduction ratio of FeO in the molten slag can achieve 99%. A novel electrolytic method with controlled oxygen flow for iron from the molten oxide slag containing FeO was proposed. The theory of electrolytic reduction with the controlled oxygen flow was developed.

  11. Increased Stability Toward Oxygen Reduction Products for Lithium-Air Batteries with Oligoether-Functionalized Silane Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Zhang, Zhengcheng; Lu, Jun; Assary, Rajeev S.; Du, Peng; Wang, Hsien-Hau; Sun, Yang-Kook; Qin, Yan; Lau, Kah Chun; Greeley, Jeffrey P.; Redfern, Paul C.; Iddir, Hakim; Curtiss, Larry A.; Amine, Khalil

    2011-12-29

    The successful development of Li-air batteries would significantly increase the possibility of extending the range of electric vehicles. There is much evidence that typical organic carbonate based electrolytes used in lithium ion batteries form lithium carbonates from reaction with oxygen reduction products during discharge in lithium-air cells so more stable electrolytes need to be found. This combined experimental and computational study of an electrolyte based on a tri(ethylene glycol)-substituted trimethylsilane (1NM3) provides evidence that the ethers are more stable toward oxygen reduction discharge species. X-ray photoelectron spectroscopy (XPS) and FTIR experiments show that only lithium oxides and no carbonates are formed when 1NM3 electrolyte is used. In contrast XPS shows that propylene carbonate (PC) in the same cell configuration decomposes to form lithium carbonates during discharge. Density functional calculations of probable decomposition reaction pathways involving solvated oxygen reduction species confirm that oligoether substituted silanes, as well as other ethers, are more stable to the oxygen reduction products than propylene carbonate. These results indicate that the choice of electrolyte plays a key role in the performance of Li-air batteries.

  12. PEALD YSZ-based bilayer electrolyte for thin film-solid oxide fuel cells

    Science.gov (United States)

    Yu, Wonjong; Cho, Gu Young; Hong, Soonwook; Lee, Yeageun; Kim, Young Beom; An, Jihwan; Cha, Suk Won

    2016-10-01

    Yttria-stabilized zirconia (YSZ) thin film electrolyte deposited by plasma enhanced atomic layer deposition (PEALD) was investigated. PEALD YSZ-based bi-layered thin film electrolyte was employed for thin film solid oxide fuel cells on nanoporous anodic aluminum oxide substrates, whose electrochemical performance was compared to the cell with sputtered YSZ-based electrolyte. The cell with PEALD YSZ electrolyte showed higher open circuit voltage (OCV) of 1.0 V and peak power density of 182 mW cm-2 at 450 °C compared to the one with sputtered YSZ electrolyte(0.88 V(OCV), 70 mW cm-2(peak power density)). High OCV and high power density of the cell with PEALD YSZ-based electrolyte is due to the reduction in ohmic and activation losses as well as the gas and electrical current tightness.

  13. Electrolytic reduction of mixed (Fe, Ti) oxide using molten calcium chloride electrolyte

    International Nuclear Information System (INIS)

    Highlights: ► Tan et al. have electrolyzed mixtures of TiO2 and Fe2O3 to produce alloys containing Fe–Ti intermetallic phases such as FeTi and Fe2Ti using the FFC process. However, the produced alloys have a porous structure with many carbon impurities, e.g., titanium carbide (TiC). Most of the carbon contamination could be caused by the presence of carbon particles in the porous alloy structure. They did not mention any obvious ways of excluding carbon and other impurities, and only suggested that the use of mixed oxides with refined structures or using a single phase, namely ilmenite (FeO·TiO2), were methods of decreasing impurities in the formed alloys. For future industrialization, there is an urgent need for obvious ways of producing purer Fe–Ti alloys with dense structures, rather than porous structures, as these absorb carbon impurities. ► Finally, we successfully reduced to a highly purified Fe–Ti intermetallic alloy of FeTi and β-Ti (FeTi4) phases. FeTi phases of size around 5–10 μm were dispersed in a matrix of the β-Ti (FeTi4) phase. The carbon content of the electrolyzed alloy was as low as less than 0.01 mass%. It was suggested that the dense structure of the alloy of FeTi and β-Ti (FeTi4) avoided the inclusion of carbon particle impurities, unlike the porous alloy structure. - Abstract: The production of high-purity metals or alloys using effective technologies is critical for future industrialization. With this aim in mind, a fundamental study of electrolysis in molten CaCl2 electrolytes was conducted to develop a new production process for ferrotitanium (Fe–Ti) intermetallic alloys. Mixed solid oxides of TiO2 and Fe2O3 were used in a molar ratio of 5.44:1.00. In this composition of Ti and Fe, FeTi and β-Ti containing iron can co-exist in equilibrium. A mixed solid (Fe, Ti) oxide was reduced electrochemically in a molten CaCl2 electrolyte at 950 °C. The metallic samples formed by electrolytic reduction of the mixed solid (Fe, Ti

  14. New polysaccharide-based polymer electrolytes; Nouveaux electrolytes polymeres a base de polysaccharides

    Energy Technology Data Exchange (ETDEWEB)

    Velasquez-Morales, P.; Le Nest, J.F.; Gandini, A. [Ecole Francaise de Papeterie et des Industries Graphique, 38 - Saint Martin d`Heres (France)

    1996-12-31

    Polysaccharides like cellulose and chitosan are known for their filmic properties. This paper concerns the synthesis and the study of chitosan-based polymer electrolytes. A preliminary work concerns the study of glucosamine reactivity. The poly-condensation of chitosan ethers (obtained by reaction with ethylene oxide or propylene oxide) with bifunctional and monofunctional oligo-ethers leads to the formation of thin lattices (10 {mu}m) having excellent mechanical properties. The presence of grafted polyether chains along the polysaccharide skeleton allows to modify the vitreous transition temperature and the molecular disorder of the system. Two type of polymer electrolytes have been synthesized: electrolytes carrying a dissolved alkaline metal salt and ionomers. The analysis of their thermal, dynamical mechanical, nuclear magnetic relaxation, electrical, and electrochemical properties shows that this new class of polymer electrolytes has the same performances as ethylene poly-oxide based amorphous lattices plus the advantage of having good filmic properties. Abstract only. (J.S.)

  15. Oxygen reduction on carbon supported platinum catalysts in high temperature polymer electrolytes

    DEFF Research Database (Denmark)

    Qingfeng, Li; Hjuler, Hans Aage; Bjerrum, Niels

    2000-01-01

    Oxygen reduction on carbon supported platinum catalysts has been investigated in H3PO4, H3PO4-doped Nafion and polybenzimidazole (PBI) polymer electrolytes in a temperature range up to 190 degrees C. Compared with pure H3PO4, the combination of H3PO4 and polymer electrolytes can significantly imp...

  16. Oxygen reduction on carbon supported platinum catalysts in high temperature polymer electrolytes

    DEFF Research Database (Denmark)

    Qingfeng, Li; Bergqvist, R. S.; Hjuler, H. A.;

    1999-01-01

    Oxygen reduction on carbon supported platinum catalysts has been investigated in H3PO4, H3PO4-doped Nafion and PBI polymer electrolytes in a temperature range from 80 to 190°C. Compared with pure H3PO4, using the H3PO4 doped Nafion and PBI polymer electrolytes can significantly improve the oxygen...

  17. Performance of Lithium Polymer Cells with Polyacrylonitrile based Electrolyte

    DEFF Research Database (Denmark)

    Perera, Kumudu; Dissanayake, M.A.K.L.; Skaarup, Steen;

    2006-01-01

    The performance of lithium polymer cells fabricated with Polyacrylonitrile (PAN) based electrolytes was studied using cycling voltammetry and continuous charge discharge cycling. The electrolytes consisted of PAN, ethylene carbonate (EC), propylene carbonate (PC) and lithium trifluoromethanesulfo......The performance of lithium polymer cells fabricated with Polyacrylonitrile (PAN) based electrolytes was studied using cycling voltammetry and continuous charge discharge cycling. The electrolytes consisted of PAN, ethylene carbonate (EC), propylene carbonate (PC) and lithium...

  18. A multiscale theoretical methodology for the calculation of electrochemical observables from ab initio data: Application to the oxygen reduction reaction in a Pt(1 1 1)-based polymer electrolyte membrane fuel cell

    International Nuclear Information System (INIS)

    In this work we present a multiscale theoretical methodology that scales up ab initio calculated data into elementary kinetic models in order to simulate Polymer Electrolyte Membrane Fuel Cells (PEMFC) transient operation. Detailed Density Functional Theory (DFT) calculations are performed on a model Pt(1 1 1) surface to determine the elementary kinetic rates of the Oxygen Reduction Reaction (ORR) mechanism at a Pt-based PEMFC cathode. These parameters include the effect of surface coverage on the activation barriers and are implemented into a Mean Field model describing the behavior of the electric field and charge distribution at the nanoscale interfacial vicinity to the catalyst, which is in turn coupled with microscale and mesoscale level models describing the charge and reactants and water transport phenomena across the cell. The impact of two possible ORR mechanisms on the simulated i–V curves is investigated: a first route connected with the dissociative adsorption of molecular oxygen on Pt(1 1 1), a second route related to the formation and the transformation of OOH surface species. The similarities and differences of the associated calculated i–V responses for each of these routes and the consequences on the interpretation of electrochemical observables at the cell level are discussed.

  19. The Pt(111)/Electrolyte Interface under Oxygen Reduction Reaction Conditions

    DEFF Research Database (Denmark)

    Bondarenko, A.S.; Stephens, Ifan; Hansen, Heine Anton;

    2011-01-01

    between the adsorbate and Pt surface atoms (0.45−1.15 V vs RHE). An equivalent electric circuit is proposed to model the Pt(111)/electrolyte interface under ORR conditions within the selected potential window. This equivalent circuit reflects three processes with different time constants, which occur...... simultaneously during the ORR at Pt(111). Density functional theory (DFT) calculations were used to correlate and interpret the results of the measurements. The calculations indicate that the coadsorption of ClO4* and Cl* with OH* is unlikely. Our analysis suggests that the two-dimensional (2D) structures formed...

  20. A Study of Electrochemical Reduction of Ethylene and PropyleneCarbonate Electrolytes on Graphite Using ATR-FTIR Spectroscopy

    Energy Technology Data Exchange (ETDEWEB)

    Zhuang, Guorong V.; Yang, Hui; Blizanac, Berislav; Ross Jr.,Philip N.

    2005-05-12

    We present results testing the hypothesis that there is a different reaction pathway for the electrochemical reduction of PC versus EC-based electrolytes at graphite electrodes with LiPF6 as the salt in common. We examined the reduction products formed using ex-situ Fourier Transform Infrared (FTIR) spectroscopy in attenuated total reflection (ATR) geometry. The results show the pathway for reduction of PC leads nearly entirely to lithium carbonate as the solid product (and presumably ethylene gas as the co-product) while EC follows a path producing a mixture of organic and inorganic compounds. Possible explanations for the difference in reaction pathway are discussed.

  1. Hyperbranched Polymer-Based Electrolyte for Lithium Polymer Batteries

    Institute of Scientific and Technical Information of China (English)

    Takahito Itoh

    2005-01-01

    @@ 1Introduction Solid polymer electrolytes have attracted much attention as electrolyte materials for all solid-state recharge able lithium batteries, and poly ( ethylene oxide) ( PEO)-based polymer electrolytes are among the most intensively studied systems[1-3]. Hyperbranched polymers have unique properties such as completely amorphous, highly soluble in common organic solvent and processible because of the highly branched nature[4,5].

  2. On the suppression of cathodic hypochlorite reduction by electrolyte additions of molybdate and chromate ions

    Directory of Open Access Journals (Sweden)

    JOHN GUSTAVSSON

    2012-11-01

    Full Text Available The goal of this study was to gain a better understanding of the feasibility of replacing Cr(VI in the chlorate process by Mo(VI, focusing on the cathode reaction selectivity for hydrogen evolution on steel and titanium in a hypochlorite containing electrolyte. To evaluate the ability of Cr(VI and Mo(VI additions to hinder hypochlorite reduction, potential sweep experiments on rotating disc electrodes and cathodic current efficiency (CE measurements on stationary electrodes were performed. Formed electrode films were investigated with scanning electron microscopy and energy-dispersive X-ray spectroscopy. Cathodic hypochlorite reduction is hindered by the Mo-containing films formed on the cathode surface after Mo(VI addition to the electrolyte, but much less efficient compared to Cr(VI addition. Very low levels of Cr(VI, in the mM range, can efficiently suppress hypochlorite reduction on polished titanium and steel. Phosphate does not negatively influence the CE in the presence of Cr(VI or Mo(VI but the Mo-containing cathode films become thinner if the electrolyte during the film build-up also contains phosphate. For a RuO2-TiO2 anode polarized in electrolyte with 40 mM Mo(VI, the anode potential increased and increased molybdenum levels were detected on the electrode surface

  3. Analysis of SEI formed with cyano-containing imidazolium-based ionic liquid electrolyte in lithium secondary batteries

    Energy Technology Data Exchange (ETDEWEB)

    Zhao, Liwei; Yamaki, Jun-ichi [Institute for Materials Chemistry and Engineering, Kyushu University, 6-1 Kasuga-Koen, Kasuga, Fukuoka 816-8580 (Japan); Egashira, Minato [Department of Applied Chemistry and Chemical Engineering, Faculty of Engineering, Yamaguchi University, 2-16-1, Yamaguchi 755-8611 (Japan)

    2007-12-06

    Two kinds of cyano-containing imidazolium-based ionic liquid, 1-cyanopropyl-3-methylimidazolium-bis(trifluoromethanesulfonyl)imide (CpMI-TFSI) and 1-cyanomethyl-3-methylimidazolium-bis(trifluoromethanesulfonyl)imide (CmMI-TFSI), each of which contained 20 wt% dissolved LiTFSI, were used as electrolytes for lithium secondary batteries. Compared with 1-ethyl-3-methylimidazolium-bis(trifluoromethane-sulfonyl)imide (EMI-TFSI) electrolyte, a reversible lithium deposition/dissolution on a stainless-steel working electrode was observed during CV measurements in these cyano-containing electrolytes, which indicated that a passivation layer (solid electrolyte interphase, SEI) was formed during potential scanning. The morphology of the working electrode with each electrolyte system was studied by SEM. Different dentrite forms were found on the electrodes with each electrolyte. The SEI that formed in CpMI-TFSI electrolyte showed the best passivating effect, while the deposited film formed in EMI-TFSI electrolyte showed no passivating effect. The chemical characteristics of the deposited films on the working electrodes were compared by XPS measurements. A component with a cyano group was found in SEIs in CpMI-TFSI and CmMI-TFSI electrolytes. The introduction of a cyano functional group suppressed the decomposition of electrolyte and improved the cathodic stability of the imidazolium-based ionic liquid. The reduction reaction route of imidazolium-based ionic liquid was considered to be different depending on whether or not the molecular structure contained a cyano functional group. (author)

  4. Ionic-Liquid-Based Polymer Electrolytes for Battery Applications.

    Science.gov (United States)

    Osada, Irene; de Vries, Henrik; Scrosati, Bruno; Passerini, Stefano

    2016-01-11

    The advent of solid-state polymer electrolytes for application in lithium batteries took place more than four decades ago when the ability of polyethylene oxide (PEO) to dissolve suitable lithium salts was demonstrated. Since then, many modifications of this basic system have been proposed and tested, involving the addition of conventional, carbonate-based electrolytes, low molecular weight polymers, ceramic fillers, and others. This Review focuses on ternary polymer electrolytes, that is, ion-conducting systems consisting of a polymer incorporating two salts, one bearing the lithium cation and the other introducing additional anions capable of plasticizing the polymer chains. Assessing the state of the research field of solid-state, ternary polymer electrolytes, while giving background on the whole field of polymer electrolytes, this Review is expected to stimulate new thoughts and ideas on the challenges and opportunities of lithium-metal batteries. PMID:26783056

  5. Highly selective determination of copper corrosion products by voltammetric reduction in a strongly alkaline electrolyte.

    Science.gov (United States)

    Nakayama, Shigeyoshi; Notoya, Takenori; Osakai, Toshiyuki

    2012-01-01

    Until recently, there had been two conflicting views about the order of copper oxides (Cu(2)O and CuO) in their cathodic reduction with a neutral or weak alkaline electrolyte (typically 0.1 M KCl). In 2001, we successfully employed a strongly alkaline electrolyte (SAE; i.e., 6 M KOH + 1 M LiOH) to achieve a perfect separation of the reduction peaks of the two oxides. It was then found that the oxides were reduced in SAE according to a thermodynamic order, i.e., "CuO → Cu(2)O", and also that the reduction of CuO occurred in one step. At an extremely slow scan rate of atmospheric corrosion of copper. PMID:22498457

  6. Modeling Joule Heating Effect on Lunar O2 Generation via Electrolytic Reduction.

    Science.gov (United States)

    Dominquez, Jesus; Poizeau, Sophie; Sibille, Laurent

    2009-01-01

    Kennedy Space Center is leading research work on lunar O2 generation via electrolytic reduction of regolith; the metal oxide present in the regolith is dissociated in oxygen anions and metal cations leading to the generation of gaseous oxygen at the anode and liquid metal at the cathode. Electrical resistance of molten regolith is high, leading to heating of the melt when electrical current is applied between the electrodes (Joule heating). The authors have developed a 3D model using a rigorous approach for two coupled physics (thermal and electrical potential) to not only study the effect of Joule heating on temperature distribution throughout the molten regolith but also to evaluate and optimize the design of the electrolytic cells. This paper presents the results of the thermal analysis performed on the model and used to validate the design of the electrolytic cell.

  7. Investigations of oxygen reduction reactions in non-aqueous electrolytes and the lithium-air battery

    Science.gov (United States)

    O'Laoire, Cormac Micheal

    Unlocking the true energy capabilities of the lithium metal negative electrode in a lithium battery has until now been limited by the low capacity intercalation and conversion reactions at the positive electrodes. This is overcome by removing these electrodes and allowing lithium to react directly with oxygen in the atmosphere forming the Li-air battery. Chapter 2 discusses the intimate role of electrolyte, in particular the role of ion conducting salts on the mechanism and kinetics of oxygen reduction in non-aqueous electrolytes designed for such applications and in determining the reversibility of the electrode reactions. Such fundamental understanding of this high energy density battery is crucial to harnessing its full energy potential. The kinetics and mechanisms of O2 reduction in solutions of hexafluorophosphate salts of the general formula X+ PF6-, where, X = tetra butyl ammonium (TBA), K, Na and Li, in acetonitrile have been studied on glassy carbon electrodes using cyclic voltammetry (CV) and rotating disk electrode (RDE) techniques. Our results show that cation choice strongly influences the reduction mechanism of O2. Electrochemical data supports the view that alkali metal oxides formed via electrochemical and chemical reactions passivate the electrode surface inhibiting the kinetics and reversibility of the processes. The O2 reduction mechanisms in the presence of the different cations have been supplemented by kinetic parameters determined from detailed analyses of the CV and RDE data. The organic solvent present in the Li+-conducting electrolyte has a major role on the reversibility of each of the O2 reduction products as found from the work discussed in the next chapter. A fundamental study of the influence of solvents on the oxygen reduction reaction (ORR) in a variety of non-aqueous electrolytes was conducted in chapter 4. In this work special attention was paid to elucidate the mechanism of the oxygen electrode processes in the rechargeable Li

  8. Physics based Degradation Modeling and Prognostics of Electrolytic Capacitors under Electrical Overstress Conditions

    Data.gov (United States)

    National Aeronautics and Space Administration — This paper proposes a physics based degradation modeling and prognostics approach for electrolytic capacitors. Electrolytic capacitors are critical components in...

  9. Prognostics Health Management and Physics based failure Models for Electrolytic Capacitors

    Data.gov (United States)

    National Aeronautics and Space Administration — This paper proposes first principles based modeling and prognostics approach for electrolytic capacitors. Electrolytic capacitors and MOSFETs are the two major...

  10. Characterization of Novel Castor Oil-Based Polyurethane Polymer Electrolytes

    OpenAIRE

    Salmiah Ibrahim; Azizan Ahmad; Nor Sabirin Mohamed

    2015-01-01

    Castor oil-based polyurethane as a renewable resource polymer has been synthesized for application as a host in polymer electrolyte for electrochemical devices. The polyurethane was added with LiI and NaI in different wt% to form a film of polymer electrolytes. The films were characterized by using attenuated total reflectance-Fourier transform infrared spectroscopy, dynamic mechanical analysis, electrochemical impedance spectroscopy, linear sweep voltammetry and transference number measurem...

  11. F{sub 4}U production by electrolytic reduction; Obtencion de UF{sub 4} por reduccion electrolitica

    Energy Technology Data Exchange (ETDEWEB)

    Esteban Duque, A.; Gispert Benach, M.; Hernandez Arroyo, F.; Montes Ponce de Leon, M.; Rojas de Diego, J. L.

    1974-07-01

    As a part of the nuclear fuel cycle program developed at the Spanish Atomic Energy Commission it has been studied the electrolytic reduction of U-VI to U-IV. The effect of the materials, electrolyte concentration, pH, current density, cell size and laboratory scale production is studied. The Pilot Plant and the production data are also described. (Author) 18 refs.

  12. Intermediate Temperature Steam Electrolysis with Phosphate-Based Electrolytes

    DEFF Research Database (Denmark)

    Prag, Carsten Brorson

    is supplied as steam. This work centred on the design and development of a novel steam electrolysis concept based on phosphate electrolytes capable of operating in the IT range. Central for the work was the selection and evaluation of the materials and components for the test setup and cells as well...... as the technological issues and challenges faced. A setup suitable for intermediate temperature electrolysis has been constructed in order to accommodate testing in the IT region. This included the evaluation of multiple generations of components such as end plates and flow plates. Chemical vapour deposition...... micro-porous layer. CsH2PO4 and Sn0.9In0.1P2O7 were used as proof-of-concept electrolytes, with emphasis on the latter electrolyte. Evaluation of electrolysis cells with these electrolytes was done with a range of tools constantly under development. These tools included regression analysis of I-V curves...

  13. ELectrolytes,water,acid—base imbalance

    Institute of Scientific and Technical Information of China (English)

    1993-01-01

    930044 The effect of dilution and heparin onthe blood gas analysis.JIANG Hongxi(蒋鸿鑫)et al.Beijing Friendship Hosp,Beijing,100050.Chin J Tubere & Respri Dis 1992;15(4):225-227.The effect of heparin on the measurement ofblood gases is mainly caused by dilution,whichsubstantially reduces the PCO2 and HCO3- val-ues.Excess heparin will change the pH,PCO2and HCO3- as a consequence of an alternation inH+ ion concentration.The effect of dilution onelectrolytes depends on the respective elec-trolyte concentration in diluent.Dilution re-duces the glucose value,but to a higher degreeas could be expected from a dilution effect.

  14. Homogeneous lithium electrodeposition with pyrrolidinium-based ionic liquid electrolytes.

    Science.gov (United States)

    Grande, Lorenzo; von Zamory, Jan; Koch, Stephan L; Kalhoff, Julian; Paillard, Elie; Passerini, Stefano

    2015-03-18

    In this study, we report on the electroplating and stripping of lithium in two ionic liquid (IL) based electrolytes, namely N-butyl-N-methylpyrrolidinium bis(fluorosulfonyl) imide (Pyr14FSI) and N-butyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (Pyr14TFSI), and mixtures thereof, both on nickel and lithium electrodes. An improved method to evaluate the Li cycling efficiency confirmed that homogeneous electroplating (and stripping) of Li is possible with TFSI-based ILs. Moreover, the presence of native surface features on lithium, directly observable via scanning electron microscope imaging, was used to demonstrate the enhanced electrolyte interphase (SEI)-forming ability, that is, fast cathodic reactivity of this class of electrolytes and the suppressed dendrite growth. Finally, the induced inhomogeneous deposition enabled us to witness the SEI cracking and revealed previously unreported bundled Li fibers below the pre-existing SEI and nonrod-shaped protuberances resulting from Li extrusion.

  15. Morphology of Polyvinylidene Fluoride Based Gel Polymer Electrolytes

    Institute of Scientific and Technical Information of China (English)

    田立颖; 黄小彬; 唐小真

    2004-01-01

    Two series of polyvinylidene fluoride (PVDF) based gel polymer electrolytes, with different LiClO4 or propylene carbonate (PC) content, were prepared and analyzed by infrared spectrometer, differential scanning calorimetry, scanning electron microscope and complex impedance spectrometer. The results show that there are great interactions between PVDF, PC and lithium cations. Both LiClO4 and PC content lead to evident change of the morphology of the gel polymer electrolytes. The content of LiClO4 and PC also influences the ionic conductivity of the samples,and an ionic conductivity of above 10-3S·cm-1 can be reached at room temperature.

  16. Li-air batteries having ether-based electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Amine, Khalil; Curtiss, Larry A; Lu, Jun; Lau, Kah Chun; Zhang, Zhengcheng; Sun, Yang-Kook

    2015-03-03

    A lithium-air battery includes a cathode including a porous active carbon material, a separator, an anode including lithium, and an electrolyte including a lithium salt and polyalkylene glycol ether, where the porous active carbon material is free of a metal-based catalyst.

  17. Lithium air batteries having ether-based electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Amine, Khalil; Curtiss, Larry A.; Lu, Jun; Lau, Kah Chun; Zhang, Zhengcheng; Sun, Yang-Kook

    2016-10-25

    A lithium-air battery includes a cathode including a porous active carbon material, a separator, an anode including lithium, and an electrolyte including a lithium salt and polyalkylene glycol ether, where the porous active carbon material is free of a metal-based catalyst.

  18. Supercapacitors based on two dimensional VO2 nanosheet electrodes in organic gel electrolyte

    KAUST Repository

    Rakhi, R.B.

    2016-10-16

    VO2 is a low band-gap semiconductor with relatively high conductivity among transition metal oxides, which makes it an interesting material for supercapacitor electrode applications. The performance of VO2 as supercapacitor electrode in organic electrolytes has never been reported before. Herein, two-dimensional nanosheets of VO2 are prepared by the simultaneous solution reduction and exfoliation from bulk V2O5 powder by hydrothermal method. A specific capacitance of 405 Fg−1 is achieved for VO2 based supercapacitor in an organic electrolyte, in three electrode configuration. The symmetric capacitor based on VO2 nanosheet electrodes and the liquid organic electrolyte exhibits an energy density of 46 Wh kg−1 at a power density of 1.4 kW kg−1 at a constant current density of 1 Ag−1. Furthermore, flexible solid-state supercapacitors are fabricated using same electrode material and Alumina-silica based gel electrolyte. The solid-state device delivers a specific capacitance of 145 Fg−1 and a device capacitance of 36 Fg−1 at a discharge current density of 1 Ag−1. Series combination of three solid state capacitors is capable of lighting up a red LED for more than 1 minute.

  19. Microporous polymer electrolyte based on PVDF-PEO

    Institute of Scientific and Technical Information of China (English)

    LI Jian; XI Jingyu; SONG Qing; TANG Xiaozhen

    2005-01-01

    @@ Since Wright et al.[1] found that the complex of PEO/alkali metals salt had the ability of ionic conductivity in 1973, in-depth studies have been carried out about various polymer electrolytes, which were applied to replacing the liquid electrolytes in lithium ion battery[2,3]. At present, polymer electrolytes mainly include three kinds: dry polymer electrolytes, gel polymer electrolytes and microporous polymer electrolytes.

  20. Advances in the electrodeposition of aluminum from ionic liquid based electrolytes

    Science.gov (United States)

    Leadbetter, Kirt C.

    Aluminum plating is of considerable technical and economic interest because it provides an eco-friendly substitute for cadmium coatings used on many military systems. However, cadmium has been determined to be a significant environmental safety and occupational health (ESOH) hazard because of its toxicity and carcinogenic nature. Furthermore, the cost of treating and disposing of generated wastes, which often contain cyanide, is costly and is becoming prohibitive in the face of increasingly stringent regulatory standards. The non-toxic alternative aluminum is equivalent or superior in performance to cadmium. In addition, it could serve to provide an alternative to hexavalent chromium coatings used on military systems for similar reasons to that of cadmium. Aluminum is a beneficial alternative in that it demonstrates self-healing corrosion resistance in the form of a tightly-bound, impervious oxide layer. A successfully plated layer would be serviceable over a wider temperature range, 925 °F for aluminum compared to 450 oF for cadmium. In addition, an aluminum layer can be anodized to make it non-conducting and colorable. In consideration of the plating process, aluminum cannot be deposited from aqueous solutions because of its reduction potential. Therefore, nonaqueous electrolytes are required for deposition. Currently, aluminum can be electrodeposited in nonaqueous processes that use hazardous chemicals such as toluene and pyrophoric aluminum alkyls. Electrodeposition from ionic liquids provides the potential for a safer method that could be easily scaled up for industrial application. The plating process could be performed at a lower temperature and higher current density than other commercially available aluminum electrodeposition processes; thus a reduced process cost could be possible. The current ionic liquid based electrolytes are more expensive; however production on a larger scale and a long electrolyte lifetime are associated with a reduction in price

  1. Improved Electrodes and Electrolytes for Dye-Based Solar Cells

    Energy Technology Data Exchange (ETDEWEB)

    Harry R. Allcock; Thomas E. Mallouk; Mark W. Horn

    2011-10-26

    The most important factor in limiting the stability of dye-sensitized solar cells is the use of volatile liquid solvents in the electrolytes, which causes leakage during extended operation especially at elevated temperatures. This, together with the necessary complex sealing of the cells, seriously hampers the industrial-scale manufacturing and commercialization feasibilities of DSSCs. The objective of this program was to bring about a significant improvement in the performance and longevity of dye-based solar cells leading to commercialization. This had been studied in two ways first through development of low volatility solid, gel or liquid electrolytes, second through design and fabrication of TiO2 sculptured thin film electrodes.

  2. Capacitance Variation of Electrolyte-Gated Bilayer Graphene Based Transistors

    Directory of Open Access Journals (Sweden)

    Hediyeh Karimi

    2013-01-01

    Full Text Available Quantum capacitance of electrolyte-gated bilayer graphene field-effect transistors is investigated in this paper. Bilayer graphene has received huge attention due to the fact that an energy gap could be opened by chemical doping or by applying external perpendicular electric field. So, this extraordinary property can be exploited to use bilayer graphene as a channel in electrolyte-gated field-effect transistors. The quantum capacitance of bi-layer graphene with an equivalent circuit is presented, and also based on the analytical model a numerical solution is reported. We begin by modeling the DOS, followed by carrier concentration as a function V in degenerate and nondegenerate regimes. To further confirm this viewpoint, the presented analytical model is compared with experimental data, and acceptable agreement is reported.

  3. Characterization of Novel Castor Oil-Based Polyurethane Polymer Electrolytes

    Directory of Open Access Journals (Sweden)

    Salmiah Ibrahim

    2015-04-01

    Full Text Available Castor oil-based polyurethane as a renewable resource polymer has been synthesized for application as a host in polymer electrolyte for electrochemical devices. The polyurethane was added with LiI and NaI in different wt% to form a film of polymer electrolytes. The films were characterized by using attenuated total reflectance-Fourier transform infrared spectroscopy, dynamic mechanical analysis, electrochemical impedance spectroscopy, linear sweep voltammetry and transference number measurement. The highest conductivity of 1.42 × 10−6 S cm−1 was achieved with the addition of 30 wt% LiI and 4.28 × 10−7 S·cm−1 upon addition of 30 wt% NaI at room temperature. The temperature dependence conductivity plot indicated that both systems obeyed Arrhenius law. The activation energy for the PU-LiI and PU-NaI systems were 0.13 and 0.22 eV. Glass transition temperature of the synthesized polyurethane decreased from −15.8 °C to ~ −26 to −28 °C upon salts addition. These characterizations exhibited the castor oil-based polyurethane polymer electrolytes have potential to be used as alternative membrane for electrochemical devices.

  4. Mechanistic study on the activity of manganese oxide catalysts for oxygen reduction reaction in an aprotic electrolyte

    International Nuclear Information System (INIS)

    Despite a large effort in catalyst research over the past decade, the benefit of electrocatalysts for the oxygen evolution reaction (OER) and especially the oxygen reduction reaction (ORR) in the aprotic Li/air battery system has not yet been clarified. Here, three nanostructured manganese oxide catalysts – namely Mn3O4, Mn5O8 and α-Mn2O3 – are investigated with regard to their activity for the ORR in a LiTFSI/DMSO electrolyte. In cyclic voltammetry (CV) measurements an overall decrease of potential gaps and an increase of re-oxidation efficiencies on carbon powder-based electrodes in comparison to glassy carbon (GC) was observed, which is attributed to the presence of more active centers, e.g. edges and kinks. Increased ORR potentials and the kinetic evaluation of the rate-determining step, namely the one-electron reduction of oxygen, point to a significantly enhanced activity of α-Mn2O3/C compared to pure carbon powder, Mn3O4/C and Mn5O8/C electrodes. This is discussed in terms of the electrocatalytic effect of α-Mn2O3 for aprotic ORR processes. The ORR activity is proposed to originate from a different reaction pathway due to coordinatively unsaturated Mn3+ ions on the surface of α-Mn2O3, which act as active centers for associative adsorption and reduction of molecular O2

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

    OpenAIRE

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

    2012-01-01

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

  6. Investigation of polymer electrolyte based on agar and ionic liquids

    Directory of Open Access Journals (Sweden)

    M. M. Silva

    2012-12-01

    Full Text Available The possibility to use natural polymer as ionic conducting matrix was investigated in this study. Samples of agarbased electrolytes with different ionic liquids were prepared and characterized by physical and chemical analyses. The ionic liquids used in this work were 1-ethyl-3-methylimidazolium ethylsulfate, [C2mim][C2SO4], 1-ethyl-3-methylimidazolium acetate, [C2mim][OAc] and trimethyl-ethanolammonium acetate, [Ch][OAc]. Samples of solvent-free electrolytes were prepared and characterized by ionic conductivity measurements, thermal analysis, electrochemical stability, X-ray diffraction, scanning electron microscopy and Fourier Transform infrared spectroscopy. Electrolyte samples are thermally stable up to approximately 190°C. All the materials synthesized are semicrystalline. The electrochemical stability domain of all samples is about 2.0 V versus Li/Li+. The preliminary studies carried out with electrochromic devices (ECDs incorporating optimized compositions have confirmed that these materials may perform as satisfactory multifunctional component layers in the field of ‘smart windows’, as well as ECD-based devices.

  7. Investigation on poly (vinylidene fluoride) based gel polymer electrolytes

    Indian Academy of Sciences (India)

    S Rajendran; P Sivakumar; Ravi Shanker Babu

    2006-12-01

    An investigation is carried out on gel polymer electrolytes consisting of poly (vinylidene fluoride) (PVdF) as a host polymer, lithium perchlorate (LiClO4), lithium triflate (LiCF3SO3) as salts and mixture of ethylene carbonate (EC) and propylene carbonate (PC) as plasticizers. Polymer thin films were prepared by solvent casting technique and the obtained films were subjected to different characterizations, to confirm their structure, complexation and thermal changes. X-ray diffraction revealed that the salts and plasticizers disrupted the crystalline nature of PVdF based polymer electrolytes and converted them into an amorphous phase. TG/DTA studies showed the thermal stability of the polymer electrolytes. The role of interaction between polymer hosts on conductivity is discussed using the results of a.c. impedance studies. Room temperature (28°C) conductivity of 2.786 × 10-3 Scm-1 was observed in PVdF (24)–EC/PC (68)–LiCF3SO3 (2)/LiClO4 (6) polymer system.

  8. CoPd x oxygen reduction electrocatalysts for polymer electrolyte membrane and direct methanol fuel cells

    International Nuclear Information System (INIS)

    The electrochemical activity of carbon-supported cobalt-palladium alloy electrocatalysts of various compositions have been investigated for the oxygen reduction reaction in a 5 cm2 single cell polymer electrolyte membrane fuel cell. The polarization experiments have been conducted at various temperatures between 30 and 60 deg. C and the reduction performance compared with data from a commercial Pt catalyst under identical conditions. Investigation of the catalytic activity of the CoPd x PEMFC system with varying composition reveals that a nominal cobalt-palladium atomic ratio of 1:3, CoPd3, exhibits the best performance of all studied catalysts, exhibiting a catalytic activity comparable to the commercial Pt catalyst. The ORR on CoPd3 has a low activation energy, 52 kJ/mol, and a Tafel slope of approximately 60 mV/decade, indicating that the rate-determining step is a chemical step following the first electron transfer step and may involve the breaking of the oxygen bond. The CoPd3 catalyst also exhibits excellent chemical stability, with the open circuit cell voltage decreasing by only 3% and the observed current decreasing by only 10% at 0.8 V over 25 h. The CoPd3 catalyst also exhibits superior tolerance to methanol crossover poisoning than Pt

  9. Non-flammable electrolytes based on trimethyl phosphate solvent for lithium-ion batteries

    Institute of Scientific and Technical Information of China (English)

    HU Chuan-yue; LI Xin-hai

    2005-01-01

    The properties of trimethyl phosphate(TMP)-based nonflammable electrolytes with LiPF6 as solute were investigated using graphite anode and LiCoO2 cathode. The effect of TMP on non-flammability of electrolytes was also evaluated. It is found that the TMP reduction decomposition on graphite electrode at the potential of 1.3V (vs Li/Li+) is suppressed with ethylene carbonate(EC), dimethyl carbonate(DMC) and ethylmethyl carbonate(EMC) cosolvents and vinylene carbonate(VC) additives. The results show that the non-flammable electrolyte of 1mol/L LiPF6 61%(EC1.5-DMC1.0-EMC1.0)-39% TMP has good electrochemical properties. The discharge capacities of half-cells after 20 cycles are 254.8mA·h/g for Li/graphite and 144.1mA·h/g for Li/LiCoO2. The graphite/LiCoO2 prismatic lithium-ion cell delivers a discharge capacity of 131mA·h/g at first cycle. With an addition of 4%VC to this non-flammable electrolyte, a discharge capacity of 134mA·h/g at first cycle and a capacity ratio of 84.3% after 50 cycles are obtained for prismatic lithium-ion batteries. Furthermore, a nail penetration test demonstrates that the safety of prismatic lithium-ion batteries is dramatically improved by using TMP-containing non-flammable electrolytes.

  10. The correlation of the properties of pyrrolidinium-based ionic liquid electrolytes with the discharge-charge performances of rechargeable Li-O2 batteries

    Science.gov (United States)

    Li, Yu; Zhang, Zhonglin; Duan, Donghong; Sun, Yanbo; Wei, Guoqiang; Hao, Xiaogang; Liu, Shibin; Han, Yunxia; Meng, Weijuan

    2016-10-01

    Pyrrolidinium-based ionic liquids (ILs), such as PYR13TFSI, PYR14TFSI, and PYR1(2O1)TFSI, exhibit high thermal and electrochemical stability with wide electrochemical windows as electrolytes for application to rechargeable Li-O2 batteries. In this work, several fundamental properties of three ILs are measured: the ionic conductivity, oxygen solubility, and oxygen diffusion coefficient. The oxygen electro-reduction kinetics is characterized using cyclic voltammetry. The performances of Li-O2 batteries with these IL electrolytes are also investigated using electrochemical impedance spectroscopy and galvanostatic discharge-charge tests. The results demonstrate that the PYR1(2O1)TFSI electrolyte battery has a higher first-discharge voltage than the PYR13TFSI electrolyte and PYR14TFSI electrolyte batteries. Both PYR13TFSI- and PYR1(2O1)TFSI-based batteries exhibit higher first-discharge capacities and better cycling stabilities than the PYR14TFSI-based battery for 30 cycles. A theoretical analysis of the experimental results shows that the diffusion coefficient and solubility of oxygen in the electrolyte remarkably affect the discharge capacity and cycling stability of the batteries. Particularly, the oxygen diffusion coefficient of the IL electrolyte can effectively facilitate the electrochemical oxygen electro-reduction reaction and oxygen concentration distribution in the catalyst layers of air electrodes. The oxygen diffusion coefficient and oxygen solubility improvements of IL electrolytes can enhance the discharge-charge performances of Li-O2 batteries.

  11. PMMA-based Gel Polymer Electrolytes with Crosslinking Network

    Institute of Scientific and Technical Information of China (English)

    H.P. Zhang; Y. P. Wu; H. Q. Wu; M. Sun

    2005-01-01

    @@ 1Introduction The lithium-ion battery has a good rate capability and low-temperature performance, but its safety is relatively low due to the possibility of leakage of liquid electrolyte. The use of a solid or gel type electrolyte can lower the probability of leakage liquid electrolyte, and the electrochemical performance of gel electrolyte doesn't decrease so markedly as the solid electrolyte. Now, new types of advanced lithium-ion battery with gel polymer electrolytes are under developing which can be used in the future.

  12. Mindfulness-Based Stress Reduction

    Science.gov (United States)

    ... R S T U V W X Y Z Mindfulness-Based Stress Reduction (MBSR) Information 5 Things You ... Better Than Usual Care Alone (03/22/16) Mindfulness Meditation May Benefit People With Chronic Insomnia (09/ ...

  13. Study on the electrolytic reduction of Uranium-VI to Uranium-IV in a nitrate system

    International Nuclear Information System (INIS)

    The determination of the best conditions to prepare hydrazine stabilized uranium (IV) nitrate solutions for utilization in Purex flowsheets is dealt with. Electrolytic reduction of U(VI) has been selected as the basic method, using an open electrolytic cell with titanum and platinum electrodes. The hydrazine concentration, the current density, acidity, U(VI) concentration and reduction time were the parameters studied and U(IV)/U(VI) ratio was used to evaluate the degree of reduction. From the results it could be concluded that the technique is reliable. The U(IV) solutions remains constant for at least two weeks and can be used in the chemical processing of irradiated uranium fuels. (Author)

  14. Kinetics and mechanism of cathodic reduction of zinc- and cadmium complexes in electrolytes containing ethanolamine and ammonia

    International Nuclear Information System (INIS)

    By the methods of plotting stationary total and partial polarograms in galvanic as well as in potentiostatic regimes the processes of cathodic zinc and cadmiun precipitation in ammonia- and ethanolamine (Etm) electrolytes have been studied versus the composition and pH of the solution. It is found that the composition of zinc- or cadmium complexes in ethanolamine-ammonia electrolytes may be presented in the form (Zn(Cd)(NHsub(3))sub(x)(Etm)sub(y)(OH)sub(z))sup(2-z), x+y+z=4; the reduction of complexes, independently of their composition, is preceded by chemical stages of partial splitting-off of ligands (or their replacement). An increase in the pH value results in appearance of insoluble salt precipitates in cadmium plating electrolytes

  15. Gelation Behavior of Poly (Vinylidene Fluoride )-based Gel Polymer Electrolyte

    Institute of Scientific and Technical Information of China (English)

    WANG Biao-bing; GU Li-xia

    2006-01-01

    Poly ( vinylidene fluoride ) ( PVdF )-based gel polymer electrolytes with various compositions were prepared by solution casting technique. The kinetics of gelation was analyzed via the correlation between the apparent gelation rate and concentration of PVdF at a given temperature.Combination the results of the kinetics of gelation and the DSC study, it revealed that the phase separation was the major behavior and the fibrils were the major junction joints of the three-dimensional network even in the ease the concentration of PVdF was higher than 25 wt%. The porous surface observed by ESEM also reflected that the phase separation took place during the gelation.

  16. A Model-Based Prognostics Methodology For Electrolytic Capacitors Based On Electrical Overstress Accelerated Aging

    Data.gov (United States)

    National Aeronautics and Space Administration — A remaining useful life prediction methodology for electrolytic capacitors is presented. This methodology is based on the Kalman filter framework and an empirical...

  17. Battery electrolytes. Citations from the NTIS data base

    Science.gov (United States)

    Young, C. G.

    1980-05-01

    Many types of solid, liquid and gaseous battery electrolytes are described and analyzed in the cited abstracts. Battery design, construction, and use, employing the listed electrolytes, are discussed. Battery design, construction, and use, employing the listed electrolytes, are discussed. Battery life, efficiency, and maintenance characteristics are also delineated. Included are 196 citations.

  18. PREPARATION AND CHARACTERIZATION OF AMIDATED PECTIN BASED POLYMER ELECTROLYTE MEMBRANES

    Institute of Scientific and Technical Information of China (English)

    R.K.Mishra; A.Anis; S.Mondal; M.Dutt; A.K.Banthia

    2009-01-01

    The work presents the synthesis and characterization of ami dated pectin(AP)based polymer electrolyte membranes(PEM)crosslinked with glutaraldehyde(GA).The prepared membranes are characterized by Fourier transform infrared spectroscopy(FTIR),organic elemental analysis,X-ray diffraction studies(XRD),thermogravimetric analysis (TGA)and impedance spectroscopy.Mechanical properties of the membranes are evaluated by tensile tests.The degree of amidation(DA),molar and mass reaction yields(YM and YN)are calculated based on the results of organic elemental analysis.FTIR spectroscopy indicated the presence of primary and secondary amide absorption bands.XRD pattern of membranes clearly indicates that there is a considerable increase in crystallinity as compared to parent pectin.TGA studies indicate that AP is less thermally stable than reference pectin.A maximum room temperature conductivity of 1.098×10-3 Scm-1 is obtained in the membrane,which is designated as AP-3.These properties make them good candidates for low cost biopolymer electrolyte membranes for fuel cell applications.

  19. Electrochemical Stability Window of Imidazolium-Based Ionic Liquids as Electrolytes for Lithium Batteries.

    Science.gov (United States)

    Kazemiabnavi, Saeed; Zhang, Zhengcheng; Thornton, Katsuyo; Banerjee, Soumik

    2016-06-30

    This paper presents the computational assessment of the electrochemical stability of a series of alkyl methylimidazolium-based ionic liquids for their use as lithium battery electrolytes. The oxidation and reduction potentials of the constituent cation and anion of each ionic liquid with respect to a Li(+)/Li reference electrode were calculated using density functional theory following the method of thermodynamic cycles, and the electrochemical stability windows (ESW)s of these ionic liquids were obtained. The effect of varying the length of alkyl side chains of the methylimidazolium-based cations on the redox potentials and ESWs was investigated. The results show that the limits of the ESWs of these methylimidazolium-based ionic liquids are defined by the oxidation potential of the anions and the reduction potential of alkyl-methylimidazolium cations. Moreover, ionic liquids with [PF6](-) anion have a wider ESW. In addition to characterizing structure-function relationships, the accuracy of the computational approach was assessed through comparisons of the data against experimental measurements of ESWs. The potentials calculated by the thermodynamic cycle method are in good agreement with the experimental data while the HOMO/LUMO method overestimates the redox potentials. This work demonstrates that these approaches can provide guidance in selecting ionic liquid electrolytes when designing high-voltage rechargeable batteries. PMID:27266487

  20. Physics Based Modeling and Prognostics of Electrolytic Capacitors

    Science.gov (United States)

    Kulkarni, Chetan; Ceyla, Jose R.; Biswas, Gautam; Goebel, Kai

    2012-01-01

    This paper proposes first principles based modeling and prognostics approach for electrolytic capacitors. Electrolytic capacitors have become critical components in electronics systems in aeronautics and other domains. Degradations and faults in DC-DC converter unit propagates to the GPS and navigation subsystems and affects the overall solution. Capacitors and MOSFETs are the two major components, which cause degradations and failures in DC-DC converters. This type of capacitors are known for its low reliability and frequent breakdown on critical systems like power supplies of avionics equipment and electrical drivers of electromechanical actuators of control surfaces. Some of the more prevalent fault effects, such as a ripple voltage surge at the power supply output can cause glitches in the GPS position and velocity output, and this, in turn, if not corrected will propagate and distort the navigation solution. In this work, we study the effects of accelerated aging due to thermal stress on different sets of capacitors under different conditions. Our focus is on deriving first principles degradation models for thermal stress conditions. Data collected from simultaneous experiments are used to validate the desired models. Our overall goal is to derive accurate models of capacitor degradation, and use them to predict performance changes in DC-DC converters.

  1. Physical properties of Li ion conducting polyphosphazene based polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Sanderson, S.; Zawodzinski, T.; Hermes, R.; Davey, J.; Dai, Hongli

    1996-12-31

    We report a systematic study of the transport properties and the underlying physical chemistry of some polyphosphazene (PPhz)-based polymer electrolytes. We synthesized MEEP and variants which employed mixed combinations of different length oxyethylene side-chains. We compare the conductivity and ion-ion interactions in polymer electrolytes obtained with lithium triflate and lithium bis(trifluoromethanesulfonyl)imide (TFSI) salts added to the polymer. The combination of the lithium imide salt and MEEP yields a maximum conductivity of 8 x 10{sup -5} {Omega}{sup -1} cm{sup -1} at room temperature at a salt loading of 8 monomers per lithium. In one of the mixed side-chain variations, a maximum conductivity of 2 x 10{sup -4} {Omega}{sup -1} cm{sup -1} was measured at the same molar ratio. Raman spectral analysis shows some ion aggregation and some polymer - ion interactions in the PPhz-LiTFSI case but much less than observed with Li CF{sub 3}SO{sub 3}. A sharp increase in the Tg as salt is added corresponds to concentrations above which the conductivity significantly decreases and ion associations appear.

  2. Preparation and physicochemical properties of surfactant-free emulsions using electrolytic-reduction ion water containing lithium magnesium sodium silicate.

    Science.gov (United States)

    Okajima, Masahiro; Wada, Yuko; Hosoya, Takashi; Hino, Fumio; Kitahara, Yoshiyasu; Shimokawa, Ken-ichi; Ishii, Fumiyoshi

    2013-04-01

    Surfactant-free emulsions by adding jojoba oil, squalane, olive oil, or glyceryl trioctanoate (medium chain fatty acid triglycerides, MCT) to electrolytic-reduction ion water containing lithium magnesium sodium silicate (GE-100) were prepared, and their physiochemical properties (thixotropy, zeta potential, and mean particle diameter) were evaluated. At an oil concentration of 10%, the zeta potential was ‒22.3 ‒ ‒26.8 mV, showing no marked differences among the emulsions of various types of oil, but the mean particle diameters in the olive oil emulsion (327 nm) and MCT emulsion (295 nm) were smaller than those in the other oil emulsions (452-471 nm). In addition, measurement of the hysteresis loop area of each type of emulsion revealed extremely high thixotropy of the emulsion containing MCT at a low concentration and the olive emulsion. Based on these results, since surfactants and antiseptic agents markedly damage sensitive skin tissue such as that with atopic dermatitis, surfactant- and antiseptic-free emulsions are expected to be new bases for drugs for external use.

  3. New polymer lithium secondary batteries based on ORMOCER (R) electrolytes-inorganic-organic polymers

    DEFF Research Database (Denmark)

    Popall, M.; Buestrich, R.; Semrau, G.;

    2001-01-01

    Based on new plasticized inorganic-organic polymer electrolytes CM. Popall, M. Andrei, J. Kappel, J. Kron, K. Olma, B. Olsowski,'ORMOCERs as Inorganic-organic Electrolytes for New Solid State Lithium Batteries and Supercapacitors', Electrochim. Acta 43 (1998) 1155] new flexible foil-batteries in ......Based on new plasticized inorganic-organic polymer electrolytes CM. Popall, M. Andrei, J. Kappel, J. Kron, K. Olma, B. Olsowski,'ORMOCERs as Inorganic-organic Electrolytes for New Solid State Lithium Batteries and Supercapacitors', Electrochim. Acta 43 (1998) 1155] new flexible foil...

  4. Luminescent polymer electrolytes based on chitosan and containing europium triflate

    Institute of Scientific and Technical Information of China (English)

    R Alves; ASS de Camargo; A Pawlicka; MM Silva

    2016-01-01

    Solid polymer electrolytes based on chitosan and europium triflate were prepared by solvent casting and characterized by X-ray diffraction, scanning electron microscopy (SEM), atomic force microscopy (AFM), and photoluminescence spectroscopy. The X-ray diffraction exhibited that the samples were essentially amorphous with organized regions over the whole range of the salt content studied. The AFM analysis demonstrated that the smoother sample had roughness of 4.39 nm. Surface visualization through SEM revealed good homogeneity without any phase separation for more conductive samples and the less conductive showed some im-perfections on the surface. The emission and excitation spectra displayed the characteristic bands of Eu(CF3SO3)3 in addition to broad bands corresponding to the polymer host. The excited state5D0 lifetime values ranged from 0.29–0.37 ms for the studied samples.

  5. Aluminum oxyhydroxide based separator/electrolyte and battery system, and a method of making the same

    Science.gov (United States)

    Gerald, II; Rex E.; Klingler, Robert J.; Rathke, Jerome W.

    2011-02-15

    The instant invention relates a solid-state electrochemical cell and a novel separator/electrolyte incorporated therein. The invented electrochemical cell generally comprising: a unique metal oxyhydroxide based (i.e. AlOOH) separator/electrolyte membrane sandwiched between a first electrode and a second electrode. The novel separator/electrolyte comprises a nanoparticulate metal oxyhydroxide, preferably AlOOH and a salt which are mixed and then pressed together to form a monolithic metal oxyhydroxide-salt membrane.

  6. Towards safer sodium-ion batteries via organic solvent/ionic liquid based hybrid electrolytes

    Science.gov (United States)

    Monti, Damien; Ponrouch, Alexandre; Palacín, M. Rosa; Johansson, Patrik

    2016-08-01

    Hybrid electrolytes aimed at application in sodium-ion batteries (SIB) consisting of an organic solvent mixture (EC:PC) and different ionic liquids (ILs); EMImTFSI, BMImTFSI, and Pyr13TFSI, and with the NaTFSI salt providing the Na+ charge carriers have here been extensively studied. The physico-chemical and electrochemical characterisation includes ionic conductivity, viscosity, density, cation coordination and solvation, various safety measures, and electrochemical stability window (ESW). Hybrid electrolytes with 10-50% of IL content were found to have ionic conductivities on par with comparable organic solvent based electrolytes, but with highly enhanced safety properties. A systematic Raman spectroscopy study of the cation coordination and solvation before and after electrolyte safety tests by ignition suggest that IL cations and TFSI remain stable when ignited while organic solvents are consumed. Finally, the solid electrolyte interphase (SEI) formed when using hybrid electrolytes has both better mechanical and electrochemical stability than the SEI derived from pure IL based electrolytes. For a half-cell with a hard carbon (HC) electrode and a hybrid electrolyte with a composition of 0.8 m NaTFSI in EC0.45:PC0.45:Pyr13TFSI0.10 encouraging results were obtained for IL based electrolytes - ca. 182 mAhg-1 at C/10 over 40 cycles.

  7. Synthesis and characterization of polyethylene oxide based nano composite electrolyte

    Indian Academy of Sciences (India)

    M Malathi; K Tamilarasan

    2014-08-01

    Polyethylene oxide (PEO) – montmorillonite (MMT) composite electrolytes were synthesised by solution casting technique. The salt used for the study is Lithium perchlorate (LiClO4). The morphology and percentage of crystallinity data were obtained through X-ray Diffraction and Differential Scanning Caloriemetry. The ionic conductivity of the polymer electrolytes was studied by impedance spectroscopy. The addition of MMT resulted in an increase in conductivity over the temperature range of 25–60°C. The ionic conductivity of a composite polymer electrolyte containing 1.2 wt% MMT was 1 × 10-5 S cm−1 at 25°C, which is at least one order of magnitude higher than that of the polymer electrolyte (4 × 10-7S cm−1). The increase in ionic conductivity is explained on the basis of crystallinity of the polymer electrolyte.

  8. PVDF-HFP-based porous polymer electrolyte membranes for lithium-ion batteries

    DEFF Research Database (Denmark)

    Miao, Ruiying; Liu, Bowen; Zhu, Zhongzheng;

    2008-01-01

    As a potential electrolyte for lithium-ion batteries, a porous polymer electrolyte membrane based on poly(vinylidenefluoride-hexafluoropropylene) (PVDF-HFP) was prepared by a phase inversion method. The casting solution, effects of the solvent and non-solvent and addition of micron scale TiO2...... particles were investigated. The membranes were characterized by SEM, XRD, AC impedance, and charge/discharge tests. By using acetone as the solvent and water as the non-solvent, the prepared membranes showed good ability to absorb and retain the lithium ion containing electrolyte. Addition of micron TiO2...... particles to the polymer electrolyte was found to enhance the tensile strength, electrolyte uptake, ion conductivity and the electrolyte/electrode interfacial stability of the membrane....

  9. Ionic liquid based lithium battery electrolytes: fundamental benefits of utilising both TFSI and FSI anions?

    Science.gov (United States)

    Kerner, M; Plylahan, N; Scheers, J; Johansson, P

    2015-07-15

    Several IL based electrolytes with an imidazolium cation (EMI) have been investigated trying to elucidate a possible beneficial effect of mixing FSI and TFSI anions in terms of physico-chemical properties and especially Li(+) solvation. All electrolytes were evaluated in terms of phase transitions, densities and viscosities, thermal stabilities, ionic conductivities and local structure, i.e. charge carriers. The electrolytes with up to 20% of Li-salts showed to be promising for high temperature lithium ion battery application (ca. 100 °C) and a synergetic effect of having mixed anions is discernible with the LiTFSI0.2EMIFSI0.8 electrolyte giving the best overall performance. The determination of the charge carriers revealed the SN to be ca. 2 for all analysed electrolytes, and proved the analysis of the mixed anion electrolytes to be challenging and inherently leads to an ambiguous picture of the Li(+) solvation. PMID:26147418

  10. Conductivity enhancement of polyacrylonitrile-based electrolytes by addition of cascade nitrile compounds

    Energy Technology Data Exchange (ETDEWEB)

    Tsutsumi, Hiromori; Matsuo, Akiko; Takase, Kimio; Doi, Shizuka; Hisanaga, Atsushi; Onimura, Kenjiro; Oishi, Tsutomu [Yamaguchi Univ. (Japan). Dept. of Applied Chemistry and Chemical Engineering

    2000-09-01

    A cascade nitrile compound ([CH{sub 2}N(CH{sub 2}CH{sub 2}CN){sub 2}]{sub 2}, ED4CN) made by addition of acrylonitrile to alkyldiamine (1,2-diaminoethane), has been used as a plasticizer for solid polymer electrolytes. The ionic conductivity of a polymer electrolyte using this type of plasticizer in polyethylene oxide (PEO)- and polyacrylonitrile (PAN)-LiClO{sub 4} complex was measured. Addition of ED4CN to PEO-based electrolytes did not enhance the conductivity of them. However, interaction between ED4CN and lithium ions in the complex was confirmed by infrared spectroscopy. The peak assigned to the stretching vibration of nitrile group in ED4CN shifted to high-energy side. The shift indicated that the nitrile groups interacted with the lithium ions in the PEO-based electrolytes. Conductivity enhancement was observed in the PAN-based electrolytes containing ED4CN. Conductivity of the electrolyte containing ED4CN was about 10 or 23 times larger than that of the electrolyte without ED4CN. Addition of ED4CN to a PAN-LiClO{sub 4} electrolyte decreases the glass transition temperature of the complexes. Conductivity enhancement of the PAN-based electrolyte with ED4CN containing lithium salt in high concentration was also confirmed. Other low molecular weight additives, tetraethylsulfamide (TESA) and a cascade nitrile compound, ([CH{sub 2}CH{sub 2}N(CH{sub 2}CH{sub 2}CN){sub 2}]{sub 2}, TE4CN) were also used and their possibility for a conducting enhancer of PAN-based electrolytes was tested. TESA was effective; however, TE4CN was inactive for a conductance enhancer of the PAN-based electrolytes. (orig.)

  11. Effects of surface chemistry and microstructure of electrolyte on oxygen reduction kinetics of solid oxide fuel cells

    Science.gov (United States)

    Park, Joong Sun; An, Jihwan; Lee, Min Hwan; Prinz, Fritz B.; Lee, Wonyoung

    2015-11-01

    We report systematic investigation of the surface properties of yttria-stabilized zirconia (YSZ) electrolytes with the control of the grain boundary (GB) density at the surface, and its effects on electrochemical activities. The GB density of thin surface layers deposited on single crystal YSZ substrates is controlled by changing the annealing temperature (750-1450 °C). Higher oxygen reduction reactions (ORR) kinetics is observed in samples annealed at lower temperatures. The higher ORR activity is ascribed to the higher GB density at the YSZ surface where 'mobile' oxide ion vacancies are more populated. Meanwhile, oxide ion vacancies concurrently created with yttrium segregation at the surface at the higher annealing temperature are considered inactive to oxygen incorporation reactions. Our results provide additional insight into the interplay between the surface chemistry, microstructures, and electrochemical activity. They potentially provide important guidelines for engineering the electrolyte-electrode interfaces of solid oxide fuel cells for higher electrochemical performance.

  12. Lithium-ion-based solid electrolyte tuning of the carrier density in graphene

    Science.gov (United States)

    Zhao, Jialin; Wang, Meng; Li, Hui; Zhang, Xuefu; You, Lixing; Qiao, Shan; Gao, Bo; Xie, Xiaoming; Jiang, Mianheng

    2016-01-01

    We have developed a technique to tune the carrier density in graphene using a lithium-ion-based solid electrolyte. We demonstrate that the solid electrolyte can be used as both a substrate to support graphene and a back gate. It can induce a change in the carrier density as large as 1 × 1014 cm−2, which is much larger than that induced with oxide-film dielectrics, and it is comparable with that induced by liquid electrolytes. Gate modulation of the carrier density is still visible at 150 K, which is lower than the glass transition temperature of most liquid gating electrolytes. PMID:27698413

  13. Electrochemical Reduction of Carbon Monoxide in Aqueous Electrolytes at Gas Diffusion Hydrophobic Electrodes

    International Nuclear Information System (INIS)

    This paper investigates the influence of the material of the electro-catalyst, the electrode composition, the type and concentration of the electrolyte, the temperature and the potential of the electrode on the electroreduction of carbon monoxide in aqueous electrolytes. The following metal powders were used as electrocatalysts: Co, Ni, Fe, Nb, Pt, W, Cu, Cd, Pb, Zn, and Raney nickel. A large series of tests showed that no organic products were synthesized in the electroysis in the presence of CO on the metals Pt, Nb, Cd, W, Cu, Pb, and Zn. The only product in the whole potential range was hydrogen, derived from the decomposition of the electrolyte. Methane, ethane, and traces of ethylene were obtained on Ni, Co, Fe, and Raney nickel. With respect to the other hydrocarbons the methane content was equal to 95%. Best results were obtained on nickel electrodes

  14. Fabrication of a micro-porous Ti–Zr alloy by electroless reduction with a calcium reductant for electrolytic capacitor applications

    Energy Technology Data Exchange (ETDEWEB)

    Kikuchi, Tatsuya, E-mail: kiku@eng.hokudai.ac.jp [Faculty of Engineering, Hokkaido University, N13-W8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Yoshida, Masumi [Faculty of Engineering, Hokkaido University, N13-W8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Taguchi, Yoshiaki [Graduate School of Chemical Science and Engineering, Hokkaido University, N13-W8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan); Habazaki, Hiroki; Suzuki, Ryosuke O. [Faculty of Engineering, Hokkaido University, N13-W8, Kita-ku, Sapporo, Hokkaido 060-8628 (Japan)

    2014-02-15

    Highlights: • A metallic Ti–Zr alloy was obtained by electroless reduction for capacitor applications. • The reduction mechanisms were studied by SEM, XRD, EPMA, and an oxygen analyzer. • The alloy was obtained by electroless reduction in the presence of excess calcium reductant. • A micro-porous Ti–Zr alloy was successfully obtained. • The alloy has a low oxygen content and a large surface area. -- Abstract: A metallic titanium and zirconium micro-porous alloy for electrolytic capacitor applications was produced by electroless reduction with a calcium reductant in calcium chloride molten salt at 1173 K. Mixed TiO{sub 2}–70 at%ZrO{sub 2} oxides, metallic calcium, and calcium chloride were placed in a titanium crucible and heated under argon atmosphere to reduce the oxides with the calcium reductant. A metallic Ti–Zr alloy was obtained by electroless reduction in the presence of excess calcium reductant and showed a micro-porous morphology due to the sintering of each of the reduced particles during the reduction. The residual oxygen content and surface area of the reduced Ti–Zr alloy decreased over time during the electroless reduction. The element distributions were slightly different at the positions of the alloy and were in the composition range of Ti-69.3 at% to 74.3 at%Zr. A micro-porous Ti–Zr alloy with low oxygen content (0.20 wt%) and large surface area (0.55 m{sup 2} g{sup −1}) was successfully fabricated by electroless reduction under optimal conditions. The reduction mechanisms of the mixed and pure oxides by the calcium reductant are also discussed.

  15. In-situ Raman spectroscopy analysis of the interfaces between Ni-based SOFC anodes and stabilized zirconia electrolyte

    CERN Document Server

    Agarkov, D A; Tsybrov, F M; Tartakovskii, I I; Kharton, V V; Bredikhin, S I

    2016-01-01

    A new experimental approach for in-situ Raman spectroscopy of the electrode | solid electrolyte interfaces in controlled atmospheres, based on the use of optically transparent single-crystal membranes of stabilized cubic zirconia, has been proposed and validated. This technique makes it possible to directly access the electrochemical reaction zone in SOFCs by passing the laser beam through single-crystal electrolyte onto the interface, in combination with simultaneous electrochemical measurements. The case study centered on the analysis of NiO reduction in standard cermet anodes under open-circuit conditions, demonstrated an excellent agreement between the observed kinetic parameters and literature data on nickel oxide. The porous cermet reduction kinetics at 400-600C in flowing H2-N2 gas mixture can be described by the classical Avrami model, suggesting that the reaction rate is determined by the metal nuclei growth limited by Ni diffusion. The advantages and limitations of the new experimental approach were...

  16. Effect of conductive additives to gel electrolytes on activated carbon-based supercapacitors

    Science.gov (United States)

    Barzegar, Farshad; Dangbegnon, Julien K.; Bello, Abdulhakeem; Momodu, Damilola Y.; Johnson, A. T. Charlie; Manyala, Ncholu

    2015-09-01

    This article is focused on polymer based gel electrolyte due to the fact that polymers are cheap and can be used to achieve extended potential window for improved energy density of the supercapacitor devices when compared to aqueous electrolytes. Electrochemical characterization of a symmetric supercapacitor devices based on activated carbon in different polyvinyl alcohol (PVA) based gel electrolytes was carried out. The device exhibited a maximum energy density of 24 Wh kg-1 when carbon black was added to the gel electrolyte as conductive additive. The good energy density was correlated with the improved conductivity of the electrolyte medium which is favorable for fast ion transport in this relatively viscous environment. Most importantly, the device remained stable with no capacitance lost after 10,000 cycles.

  17. Effect of conductive additives to gel electrolytes on activated carbon-based supercapacitors

    Directory of Open Access Journals (Sweden)

    Farshad Barzegar

    2015-09-01

    Full Text Available This article is focused on polymer based gel electrolyte due to the fact that polymers are cheap and can be used to achieve extended potential window for improved energy density of the supercapacitor devices when compared to aqueous electrolytes. Electrochemical characterization of a symmetric supercapacitor devices based on activated carbon in different polyvinyl alcohol (PVA based gel electrolytes was carried out. The device exhibited a maximum energy density of 24 Wh kg−1 when carbon black was added to the gel electrolyte as conductive additive. The good energy density was correlated with the improved conductivity of the electrolyte medium which is favorable for fast ion transport in this relatively viscous environment. Most importantly, the device remained stable with no capacitance lost after 10,000 cycles.

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

    Directory of Open Access Journals (Sweden)

    Ayan Ghosh

    2012-01-01

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

  19. Role of Chloride for a Simple, Non-Grignard Mg Electrolyte in Ether-Based Solvents.

    Science.gov (United States)

    Sa, Niya; Pan, Baofei; Saha-Shah, Anumita; Hubaud, Aude A; Vaughey, John T; Baker, Lane A; Liao, Chen; Burrell, Anthony K

    2016-06-29

    Mg battery operates with Chevrel phase (Mo6S8, ∼1.1 V vs Mg) cathodes that apply Grignard-based or derived electrolytes, which allow etching of the passivating oxide coating forms at the magnesium metal anode. Majority of Mg electrolytes studied to date are focused on developing new synthetic strategies to achieve a better reversible Mg deposition. While most of these electrolytes contain chloride as a component, and there is a lack of literature which investigates the fundamental role of chloride in Mg electrolytes. Further, ease of preparation and potential safety benefits have made simple design of magnesium electrolytes an attractive alternative to traditional air sensitive Grignard reagents-based electrolytes. Work presented here describes simple, non-Grignard magnesium electrolytes composed of magnesium bis(trifluoromethane sulfonyl)imide mixed with magnesium chloride (Mg(TFSI)2-MgCl2) in tetrahydrofuran (THF) and diglyme (G2) that can reversibly plate and strip magnesium. Based on this discovery, the effect of chloride in the electrolyte complex was investigated. Electrochemical properties at different initial mixing ratios of Mg(TFSI)2 and MgCl2 showed an increase of both current density and columbic efficiency for reversible Mg deposition as the fraction content of MgCl2 increased. A decrease in overpotential was observed for rechargeable Mg batteries with electrolytes with increasing MgCl2 concentration, evidenced by the coin cell performance. In this work, the fundamental understanding of the operation mechanisms of rechargeable Mg batteries with the role of chloride content from electrolyte could potentially bring rational design of simple Mg electrolytes for practical Mg battery. PMID:27255422

  20. Kinetic factors determining conducting filament formation in solid polymer electrolyte based planar devices.

    Science.gov (United States)

    Krishnan, Karthik; Aono, Masakazu; Tsuruoka, Tohru

    2016-08-01

    Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength, and the reduction sites for precipitation. Different filament formations, resulting from unidirectional and dendritic growth behaviours, can be controlled by tuning specified parameters, which in turn improves the stability and performance of SPE-based devices.

  1. Effect of some non functional surfactants and electrolytes on the hexavalent chromium reduction by glycerol. A mechanistic study

    Energy Technology Data Exchange (ETDEWEB)

    Basu, A.; Ghosh, S.K.; Saha, R.; Nandi, R.; Saha, B. [Burdwan Univ., WB (India). Dept. of Chemistry; Gosh, T. [A.B.N. Seal College, Coochbehar, WB (India). Dept. of Chemistry

    2011-11-15

    Hexavalent chromium is a widespread environmental contaminant and a known human carcinogen. Kinetics of reduction of hexavalent chromium by bio-molecule glycerol in micellar media have been studied spectrophotometrically. The cytoplasmic reduction of hexavalent chromium to trivalent chromium occurs in micro-heterogeneous systems. In vitro, the micelles are considered to mimic the cellular membranes. The electron transfer processes occurring in the micellar systems is considered as model to obtain insight into the electron transport process prevailing in biological systems. Micellar media is also a probe to establish the mechanistic paths of reduction of hexavalent chromium to trivalent chromium. Effects of electrolytes common to biological system are studied to establish the proposed reaction mechanism strongly. (orig.)

  2. Cellulose based Lithium ion polymer electrolytes for Lithium batteries

    OpenAIRE

    Chelmecki, Marcin

    2004-01-01

    The separator membrane in batteries and fuel cells is of crucial importance for the function of these devices. In lithium ion batteries the separator membrane as well as the polymer matrix of the electrodes consists of polymer electrolytes which are lithium ion conductors. To overcome the disadvantage of currently used polymer electrolytes which are highly swollen with liquids and thus mechanically and electrochemically unstable, the goal of this work is a new generation of solid polymer e...

  3. Development of fractional order capacitors based on electrolyte processes

    OpenAIRE

    Jesus, Isabel S.; Machado, J. A. Tenreiro

    2009-01-01

    In recent years, significant research in the field of electrochemistry was developed. The performance of electrical devices, depending on the processes of the electrolytes, was described and the physical origin of each parameter was established. However, the influence of the irregularity of the electrodes was not a subject of study and only recently this problem became relevant in the viewpoint of fractional calculus. This paper describes an electrolytic process in the perspective of fraction...

  4. Photoelectrochemical solar cells with polyacrylonitrile-based and polyethylene oxide-based polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Ileperuma, O.A.; Somasunderam, S. [University of Peradeniya (Sri Lanka). Dept. of Chemistry; Dissanayake, M.A.K.L.; Bandara, L.R.A.K. [University of Peradeniya (Sri Lanka). Dept. of Physics

    2004-10-01

    Two types of photoelectrochemical (PEC) solar cells, FTO/TiO{sub 2}/dye/PAN, EC, PC, Pr{sub 4}N{sup +-}, I{sub 2}/Pt/FTO, and FTO/TiO{sub 2}/dye/PEO, EC, PC, KI/I{sub 2}{sup P}t /FTO have been fabricated using a PAN-based gel polymer electrolyte and a PEO-based plasticised polymer electrolyte. The PAN-based gel electrolyte, made of polyacrylonitrile (PAN), ethylene carbonate (EC), propylene carbonate (PC) and tetrapropylammoniumiodide (Pr{sub 4}N{sup +-}) as the completing salt exhibited a room temperature conductivity of 2.9 x 10{sup -1} S m{sup -1} for the composition, PAN (13%):EC (31%):PC (45%):Pr{sub 4}N{sup +}I{sup -} (7%):I{sub 2} (4%) by weight ratio. The PEO-based polymer electrolyte had a conductivity of 2.2 x 10{sup -3} S cm{sup -1} for the composition PEO (37.5%):EC (37.5%):PC (20.7%):KI (3.9%):12 (0.4%). These solar cells have been characterised using current-voltage characteristics and action spectra. The PAN-based solar cells had an overall quantum efficiency of 2.3%. However, the PEO-based solar cells had an overall quantum efficiency of only 0.6%. (author)

  5. Triol Based Polyurethane Gel Electrolytes for Electrochemical Devices

    Science.gov (United States)

    Kulkarni, A. R.

    2006-06-01

    Polyurethane gel electrolytes with various solvents such as propylene carbonate (PC), propylene carbonate - ethylene carbonate (PC-EC) and γ-butyrolactone - ethylene carbonate (GBL-EC) were synthesized and studied by different characterization tools. Impedance spectroscopy and nuclear magnetic resonance spectroscopy (NMR) provides the insight on ionic mobility in the gel electrolyte. The syneresis effect was studied by observing the weight loss as a function of time. Morphology of the gel electrolyte was investigated by ESEM. Among the various compositions, the maximum conductivity was observed for 35%PU-60%EC/GBL-5%LiClO4. The maximum conductivity of gel electrolytes was found to be 3.98 × 10-3 S/cm at the room temperature, which is higher than that reported in the domain of published literature for the thermoplastic polyurethane family. Moreover, merely 3.5% weight loss was observed for the period of 30 days. The 3.5% wt solvent loss has negligible effect on the conductivity of the gel electrolyte. Test cell was fabricated using polyurethane gel electrolyte and discharge characteristic was studied.

  6. Poly(vinylidene fluoride-hexafluoropropylene) polymer electrolyte for paper-based and flexible battery applications

    Science.gov (United States)

    Aliahmad, Nojan; Shrestha, Sudhir; Varahramyan, Kody; Agarwal, Mangilal

    2016-06-01

    Paper-based batteries represent a new frontier in battery technology. However, low-flexibility and poor ionic conductivity of solid electrolytes have been major impediments in achieving practical mechanically flexible batteries. This work discuss new highly ionic conductive polymer gel electrolytes for paper-based battery applications. In this paper, we present a poly(vinylidene fluoride-hexafluoropropylene) (PVDH-HFP) porous membrane electrolyte enhanced with lithium bis(trifluoromethane sulphone)imide (LiTFSI) and lithium aluminum titanium phosphate (LATP), with an ionic conductivity of 2.1 × 10-3 S cm-1. Combining ceramic (LATP) with the gel structure of PVDF-HFP and LiTFSI ionic liquid harnesses benefits of ceramic and gel electrolytes in providing flexible electrolytes with a high ionic conductivity. In a flexibility test experiment, bending the polymer electrolyte at 90° for 20 times resulted in 14% decrease in ionic conductivity. Efforts to further improving the flexibility of the presented electrolyte are ongoing. Using this electrolyte, full-cell batteries with lithium titanium oxide (LTO) and lithium cobalt oxide (LCO) electrodes and (i) standard metallic current collectors and (ii) paper-based current collectors were fabricated and tested. The achieved specific capacities were (i) 123 mAh g-1 for standard metallic current collectors and (ii) 99.5 mAh g-1 for paper-based current collectors. Thus, the presented electrolyte has potential to become a viable candidate in paper-based and flexible battery applications. Fabrication methods, experimental procedures, and test results for the polymer gel electrolyte and batteries are presented and discussed.

  7. A new ether-based electrolyte for dendrite-free lithium-metal based rechargeable batteries

    Science.gov (United States)

    Miao, Rongrong; Yang, Jun; Xu, Zhixin; Wang, Jiulin; Nuli, Yanna; Sun, Limin

    2016-02-01

    A new ether-based electrolyte to match lithium metal electrode is prepared by introducing 1, 4-dioxane as co-solvent into lithium bis(fluorosulfonyl)imide/1,2-dimethoxyethane solution. Under the synergetic effect of solvents and salt, this simple liquid electrolyte presents stable Li cycling with dendrite-free Li deposition even at relatively high current rate, high coulombic efficiency of ca. 98%, and good anodic stability up to ~4.87 V vs Li RE. Its excellent performance will open up a new possibility for high energy-density rechargeable Li metal battery system.

  8. A new ether-based electrolyte for dendrite-free lithium-metal based rechargeable batteries

    OpenAIRE

    Rongrong Miao; Jun Yang; Zhixin Xu; Jiulin Wang; Yanna Nuli; Limin Sun

    2016-01-01

    A new ether-based electrolyte to match lithium metal electrode is prepared by introducing 1, 4-dioxane as co-solvent into lithium bis(fluorosulfonyl)imide/1,2-dimethoxyethane solution. Under the synergetic effect of solvents and salt, this simple liquid electrolyte presents stable Li cycling with dendrite-free Li deposition even at relatively high current rate, high coulombic efficiency of ca. 98%, and good anodic stability up to ~4.87 V vs Li RE. Its excellent performance will open up a new ...

  9. Reduction of robot base parameters

    International Nuclear Information System (INIS)

    This paper is a new step in the search of minimum dynamic parameters of robots. In spite of planing exciting trajectories and using base parameters, some parameters remain not identifiable due to the perturbation effects. In this paper, we propose methods to reduce the set of base parameters in order to get an essential set of parameters. This new set defines a simplified identification model witch improves the noise immunity of the estimation process. It contributes also in reducing the computation burden of a simplified dynamic model. Different methods are proposed and are classified in two parts: methods, witch perform reduction and identification together, come from statistical field and methods, witch reduces the model before the identification thanks to a priori information, come from numerical field like the QR factorization. Statistical tools and QR reduction are shown to be efficient and adapted to determine the essential parameters. They can be applied to open-loop, or graph structured rigid robot, as well as flexible-link robot. Application for the PUMA 560 robot is given. (authors). 9 refs., 4 tabs

  10. Polymer electrolytes based on aromatic lithium sulfonyl-imide compounds; Electrolytes polymeres a base de sulfonylimidures de lithium aromatiques

    Energy Technology Data Exchange (ETDEWEB)

    Reibel, L.; Bayoudh, S. [Centre National de la Recherche Scientifique (CNRS), 67 - Strasbourg (France). Institut Charles Sadron; Baudry, P. [Electricite de France, 77 - Moret sur Loing (France). Direction des Etudes et Recherches; Majastre, H. [Bollore Technologies, 29 - Quimper (France); Herlem, G. [UFR de Sciences et Techniques, L.E.S., 25 - Besancon (France)

    1996-12-31

    This paper presents ionic conductivity results obtained with polymer electrolytes and also with propylene carbonate solutions. The domain of electrochemical activity of this salt has been determined using cycle volt-amperometry in propylene carbonate. Preliminary experiments on the stability of the polymer electrolyte with respect to the lithium electrode have been carried out for a possible subsequent use in lithium batteries. (J.S.) 4 refs.

  11. NMR study of starch based polymer gel electrolytes: Humidity effects

    International Nuclear Information System (INIS)

    In this work, nuclear magnetic resonance spectroscopy (NMR) was used to study the effect of water absorption in polymer gel electrolytes formed by amylopectin rich starch, plasticized with glycerol and containing lithium perchlorate. The position of the 7Li spin-lattice relaxation rate maximum is shifted progressively towards lower temperatures with increasing hydration, reflecting an increase of the lithium mobility. The mechanism responsible for the spin-lattice relaxation of the 7Li nuclei in the gel electrolytes are the fluctuations of the quadrupolar interaction due to the lithium motions. The 7Li relaxation results of the gel electrolyte hydrated with 2.2 water per complex unit suggest that the lithium ions are almost decoupled from the polymer chain and coordinate, hence preferring the water molecules

  12. Understanding ternary poly(potassium benzimidazolide)-based polymer electrolytes

    DEFF Research Database (Denmark)

    Aili, David; Jankova Atanasova, Katja; Han, Junyoung;

    2016-01-01

    Poly(2,20-(m-phenylene)-5,50-bisbenzimidazole) (m-PBI) can dissolve large amounts of aqueous electrolytes to give materials with extraordinary high ion conductivity and the practical applicability has been demonstrated repeatedly in fuel cells, water electrolysers and as anion conducting component...

  13. Preparation and properties of biodegradable polymer-layered silicate nanocomposite electrolytes for zinc based batteries

    International Nuclear Information System (INIS)

    Highlights: • Organically modified MMT is used as nanofiller to enhance the properties of the polymer PCL-zinc triflate salt complex. • The nanocomposite showed enhancement in conductivity, excellent electrochemical and thermal stability. • Cyclic voltammetry revealed feasibility of intercalation/deintercalation of Zn2+ ions with MnO2 cathode. • Best conducting electrolyte showed remarkable degradability in soil compost over a period of 90 days. - Abstract: Polymer-layered silicate nanocomposite electrolytes (PLSNEs) were prepared by utilizing a biodegradable polymer namely poly(ϵ-caprolactone) as host polymer and zinc triflate as dopant salt with the incorporation of varying concentrations of octadecylamine modified montmorillonite nanoclay and further characterized using various experimental techniques. A maximum conductivity of 9.5 × 10−5 S cm−1 was achieved for a 15 wt% loading of the nanoclay. X-ray diffraction and differential scanning calorimetric studies revealed the change occurring in the crystalline behavior of the electrolyte as a result of incorporation of the nanoclay. An appreciably good thermal and electrochemical stability was also observed thus suggesting applicability of the prepared electrolyte in commericial systems and therefore the feasibility of reduction and oxidation processes of MnO2 cathode with the prepared electrolyte system has also been evaluated by means of cyclic voltammetry. The best conducting sample of the polymer electrolyte showed a remarkable degradability over a degradation period of 90 days in soil compost

  14. Lithium-sulfur batteries based on nitrogen-doped carbon and an ionic-liquid electrolyte.

    Science.gov (United States)

    Sun, Xiao-Guang; Wang, Xiqing; Mayes, Richard T; Dai, Sheng

    2012-10-01

    Nitrogen-doped mesoporous carbon (NC) and sulfur were used to prepare an NC/S composite cathode, which was evaluated in an ionic-liquid electrolyte of 0.5 M lithium bis(trifluoromethane sulfonyl)imide (LiTFSI) in methylpropylpyrrolidinium bis(trifluoromethane sulfonyl)imide ([MPPY][TFSI]) by cyclic voltammetry (CV), electrochemical impedance spectroscopy (EIS), and cycle testing. To facilitate the comparison, a C/S composite based on activated carbon (AC) without nitrogen doping was also fabricated under the same conditions. Compared with the AC/S composite, the NC/S composite showed enhanced activity toward sulfur reduction, as evidenced by the lower onset sulfur reduction potential, higher redox current density in the CV test, and faster charge-transfer kinetics, as indicated by EIS measurements. At room temperature under a current density of 84 mA g(-1) (C/20), the battery based on the NC/S composite exhibited a higher discharge potential and an initial capacity of 1420 mAh g(-1), whereas the battery based on the AC/S composite showed a lower discharge potential and an initial capacity of 1120 mAh g(-1). Both batteries showed similar capacity fading with cycling due to the intrinsic polysulfide solubility and the polysulfide shuttle mechanism; capacity fading can be improved by further cathode modification. PMID:22847977

  15. Direct Electrolytic Reduction of Solid Ta2O5 to Ta with SOM Process

    Science.gov (United States)

    Chen, Chaoyi; Yang, Xiaqiong; Li, Junqi; Lu, Xionggang; Yang, Shufeng

    2016-06-01

    A process that uses the solid-oxide-oxygen-ion conducting membrane has been investigated to produce tantalum directly from solid Ta2O5 in molten CaCl2 or a molten mixture of 55.5MgF2-44.5CaF2 (in wt pct). The sintered porous Ta2O5 pellet was employed as the cathode, while the liquid copper alloy, saturated with graphite powder and encased in a one-end-closed yttria-stabilized-zirconia (YSZ) tube, acted as the anode. The electrolysis potential in this method is higher than that of the Fray-Farthing-Chen Cambridge process because the YSZ membrane tube blocks the melts to electrolyze, and only Ta2O5 is will be electrolyzed. The microstructures of reduced pellets and a cyclic voltammogram of solid Ta2O5 in molten CaCl2 were analyzed. In addition, the influence of particle size and porosity of the cathode pellets on metal-oxide-electrolyte, three-phase interlines was also discussed. The results demonstrate that the sintering temperature of cathode pellets and electrolytic temperature play important roles in the electrochemical process. Furthermore, this process can be used to produce Ta metal efficiently without the expensive cost of pre-electrolysis and generation of harmful by-products.

  16. Aluminum oxyhydroxide based separator/electrolyte and battery system, and a method making the same

    Science.gov (United States)

    Gerald, II, Rex E.; Klingler, Robert J.; Rathke, Jerome W.

    2011-03-08

    The instant invention relates a solid-state electrochemical cell and a novel separator/electrolyte incorporated therein. A preferred embodiment of the invented electrochemical cell generally comprises a unique metal oxyhydroxide based (i.e. AlOOH) separator/electrolyte membrane sandwiched between a first electrode and a second electrode. A preferred novel separator/electrolyte comprises a nanoparticulate metal oxyhydroxide, preferably AlOOH and a salt which are mixed and then pressed together to form a monolithic metal oxyhydroxide-salt membrane.

  17. Dielectric behavior of different nanofillers incorporated in PVC-PMMA based polymer electrolyte membranes

    Science.gov (United States)

    Sowmya, G.; Pradeepa, P.; Kalaiselvimary, J.; Edwinraj, S.; Prabhu, M. Ramesh

    2016-05-01

    The Poly (methyl methacrylate) (PMMA)-Poly (vinyl chloride) (PVC) based polymer electrolytes were prepared by solvent casting technique. The prepared polymer electrolytes were subjected to conductivity studies by using electrochemical impedance spectroscopy and the maximum ionic conductivity value was found to be 0.8011 × 10-3 Scm-1 at 303K for PVC (17.5wt%) - PMMA (7.5wt %) - LiClO4 (8wt %) - PC (67wt %) - BaTiO3 (8wt%) electrolyte system. The dielectric behavior of the samples also studied.

  18. Study on the Ion Association in PVdF-based Gel Polymer Electrolyte

    Institute of Scientific and Technical Information of China (English)

    2006-01-01

    Gel polymer electrolytes based on the poly (vinylidene fluoride) (PVdF) and the electrolyte of LiClO4 in propylene carbonate (PC) were prepared by the solution casting technique. The ionic conductivity of the gel electrolytes was concentration of lithium salt. Because of the strong coulombiq attractions, the dissolved salt ions might aggregate into ion pairs and multiple ion aggregates. The analysis of DSC and X-ray diffraction revealed that the ions association occurred at higher concentration of lithium salt.

  19. Highly dispersed TaOx nanoparticles prepared by electrodeposition as oxygen reduction electrocatalysts for polymer electrolyte fuel cells

    KAUST Repository

    Seo, Jeongsuk

    2013-06-06

    Based on the chemical stability of group IV and V elements in acidic solutions, TaOx nanoparticles prepared by electrodeposition in an ethanol-based Ta plating bath at room temperature were investigated as novel nonplatinum electrocatalysts for the oxygen reduction reaction (ORR) in polymer electrolyte fuel cells (PEFCs). Electrodeposition conditions of Ta complexes and subsequent various heat treatments for the deposited TaOx were examined for the best performance of the ORR. TaOx particles on carbon black (CB), electrodeposited at a constant potential of -0.5 V Ag/AgCl for 10 s and then heat-treated by pure H2 flow at 523 K for 1 h, showed excellent catalytic activity with an onset potential of 0.93 VRHE (for 2 μA cm-2) for the ORR. Surface characterizations of the catalysts were performed by scanning transmission electron microscopy (STEM), transmission electron microscopy (TEM), and energy dispersive X-ray spectroscopy (EDS). The loading amounts of the electrodeposited material on the CB were determined by inductively coupled plasma atomic emission spectroscopy (ICP-AES). All the physical results suggested that high dispersion of TaOx particles on the CB surface with 2-3 nm size was critical and key for high activity. The chemical identity and modified surface structure for the deposited TaOx catalysts before and after H 2 heat treatment were analyzed by X-ray photoelectron spectroscopy (XPS). The formation of more exposed active sites on the electrode surface and enhanced electroconductivity of the tantalum oxide promoted from the H 2 treatment greatly improved the ORR performance of the electrodeposited TaOx nanoparticles on CB. Finally, the highly retained ORR activity after an accelerated durability test in an acidic solution confirmed and proved the chemical stability of the oxide nanoparticles. The high utilization of the electrodeposited TaOx nanoparticles uniformly dispersed on CB for the ORR was comparable to that of commercial Pt/CB catalysts

  20. Enhanced photocurrent generation in bacteriorhodopsin based bio-sensitized solar cells using gel electrolyte.

    Science.gov (United States)

    Chellamuthu, Jeganathan; Nagaraj, Pavithra; Chidambaram, Sabari Girisun; Sambandam, Anandan; Muthupandian, Ashokkumar

    2016-09-01

    High purity light sensitive photoactive protein Bacteriorhodopsin (BR) was isolated successfully via a simple two phase extraction technique (ATPS) as an alternate method for the tedious sucrose gradient ultracentrifugation procedure (SGU). Bio sensitized solar cells (BSSCs) were fabricated by the integration of BR into TiO2 (photo anode) with acetamide based gel electrolytes and platinum (photo cathode) as a counter electrode. The structural and photoelectrical behaviours of BR and BSSCs were analyzed by Atomic Force Microscopy, Raman spectroscopy, photocurrent and photovoltage (IV) measurement and electrochemical impedance spectroscopy. The short circuit photocurrent (Jsc) and photoelectric conversion efficiency (η) of acetamide based gel electrolyte (AG) (1.08mAcm(-2), 0.49%) are twice higher than that of traditional triiodide based liquid electrolyte (LE) (0.62mAcm(-2), 0.19%). Also, quasi-Fermi level and lifetime of photogenerated electrons in acetamide based gel electrolyte is about four times higher than that observed in traditional triiodide redox electrolyte. A comparison of the observed results with similar BSSCs made of other natural photoactive protein systems shows that BR as sensitizer has better photovoltaic performance. The enhanced photocurrent generation of the BSSC constructed in our study could be due to the interaction of BR with acetamide based modified poly(ethylene)oxide (PEO) gel electrolyte. PMID:27380296

  1. Polymer Electrolyte Fuel Cells Employing Heteropolyacids as Redox Mediators for Oxygen Reduction Reactions: Pt-Free Cathode Systems.

    Science.gov (United States)

    Matsui, Toshiaki; Morikawa, Eri; Nakada, Shintaro; Okanishi, Takeou; Muroyama, Hiroki; Hirao, Yoshifumi; Takahashi, Tsuyoshi; Eguchi, Koichi

    2016-07-20

    In this study, the heteropolyacids of H3+xPVxMO12-xO40 (x = 0, 2, and 3) were applied as redox mediators for the oxygen reduction reaction in polymer electrolyte fuel cells, of which the cathode is free from the usage of noble metals such as Pt/C. In this system, the electrochemical reduction of heteropolyacid over the carbon cathode and the subsequent reoxidation of the partially reduced heteropolyacid by exposure to the dissolved oxygen in the regenerator are important processes for continuous power generation. Thus, the redox properties of catholytes containing these heteropolyacids were investigated in detail. The substitution quantity of V in the heteropolyacid affected the onset reduction potential as well as the reduction current density, resulting in a difference in cell performance. The chemical composition of heteropolyacid also had a significant impact on the reoxidation property. Among the three compounds, H6PV3Mo9O40 was the most suitable redox mediator. Furthermore, the pH of the catholyte was found to be the crucial factor in determining the reoxidation rate of partially reduced heteropolyacid as well as cell performance. PMID:27348019

  2. Structural and Electrochemical Analysis of PMMA Based Gel Electrolyte Membranes

    Directory of Open Access Journals (Sweden)

    Chithra M. Mathew

    2015-01-01

    Full Text Available New gel polymer electrolytes containing poly(vinylidene chloride-co-acrylonitrile and poly(methyl methacrylate are prepared by solution casting method. With the addition of 60 wt.% of EC to PVdC-AN/PMMA blend, ionic conductivity value 0.398×10-6 S cm−1 has been achieved. XRD and FT-IR studies have been conducted to investigate the structure and complexation in the polymer gel electrolytes. The FT-IR spectra show that the functional groups C=O and C≡N play major role in ion conduction. Thermal stability of the prepared membranes is found to be about 180°C.

  3. Lanthanum germanate-based apatites as electrolyte for SOFCs

    Energy Technology Data Exchange (ETDEWEB)

    Marrero-Lopez, D.; Diaz-Carrasco, P.; Ramos-Barrado, J.R. [Departamento de Fisica Aplicada I, Laboratorio de Materiales y Superficies (Unidad Asociada al C.S.I.C.), Universidad de Malaga, 29071 Malaga (Spain); Pena-Martinez, J. [Instituto de Energias Renovables, Parque Tecnologico, Universidad de Castilla La Mancha, 02006 Albacete (Spain); Ruiz-Morales, J.C. [Departamento de Quimica Inorganica, Universidad de La Laguna, 38200 La Laguna, Tenerife (Spain)

    2011-02-15

    Germanate apatites with composition La{sub 10-x}Ge{sub 5.5}Al{sub 0.5}O{sub 26.75-3x/2} have been evaluated for the first time as possible electrolytes for solid oxide fuel cells (SOFCs). Different electrode materials have been considered in this study, i.e. manganite, ferrite, nickelates and cobaltite as cathode materials; and NiO-CGO composite and chromium-manganite as anodes. The chemical compatibility and electrochemical performance of these electrodes with La{sub 9.8}Ge{sub 5.5}Al{sub 0.5}O{sub 26.45} have been studied by X-ray powder diffraction (XRPD) and impedance spectroscopy. The XRPD analysis did not reveal appreciable bulk reactivity with the formation of reaction products between the germanate electrolyte and these electrodes up to 1,200 C. However, a significant cation interdiffusion was observed by energy dispersive spectroscopy (EDS) at the electrode/electrolyte interface, which leads to a significant decrease of the performance of these electrodes. (Copyright copyright 2011 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  4. Sequential separation of transuranic elements and fission products from uranium metal ingots in electrolytic reduction process of spent PWR fuels

    International Nuclear Information System (INIS)

    A sequential separation procedure has been developed for the determination of transuranic elements and fission products in uranium metal ingot samples from an electrolytic reduction process for a metallization of uranium dioxide to uranium metal in a medium of LiCl-Li2O molten salt at 650 deg C. Pu, Np and U were separated using anion-exchange and tri-n-butylphosphate (TBP) extraction chromatography. Cs, Sr, Ba, Ce, Pr, Nd, Sm, Eu, Gd, Zr and Mo were separated in several groups from Am and Cm using TBP and di(2-ethylhexyl)phosphoric acid (HDEHP) extraction chromatography. Effect of Fe, Ni, Cr and Mg, which were corrosion products formed through the process, on the separation of the analytes was investigated in detail. The validity of the separation procedure was evaluated by measuring the recovery of the stable metals and 239Pu, 237Np, 241Am and 244Cm added to a synthetic uranium metal ingot dissolved solution. (author)

  5. LiCl salt waste treatment generated from electrolytic reduction process of spent oxide fuel by melt crystallization process

    International Nuclear Information System (INIS)

    The effects of operating conditions such as crystal growing rate and initial impurity concentration on separation(or concentration) of cesium and strontium fission products involved in a LiCl waste salt generated from an electrolytic reduction process of a spent oxides by a lab-scale layer melt crystallization process were analyzed. In a layer crystallization process, impurities(CsCl and SrCl2) are concentrated in a small part of the LiCl salt by the solubility difference between a melt phase and a crystal phase. The crystal growth rate strongly affects the crystal structure, therefore the separation efficiency, but the effect of the initial Cs and Sr concentration in LiCl molten salts was nearly negligible within an experimental range. (author)

  6. A Model-based Prognostics Methodology for Electrolytic Capacitors Based on Electrical Overstress Accelerated Aging

    Science.gov (United States)

    Celaya, Jose; Kulkarni, Chetan; Biswas, Gautam; Saha, Sankalita; Goebel, Kai

    2011-01-01

    A remaining useful life prediction methodology for electrolytic capacitors is presented. This methodology is based on the Kalman filter framework and an empirical degradation model. Electrolytic capacitors are used in several applications ranging from power supplies on critical avionics equipment to power drivers for electro-mechanical actuators. These devices are known for their comparatively low reliability and given their criticality in electronics subsystems they are a good candidate for component level prognostics and health management. Prognostics provides a way to assess remaining useful life of a capacitor based on its current state of health and its anticipated future usage and operational conditions. We present here also, experimental results of an accelerated aging test under electrical stresses. The data obtained in this test form the basis for a remaining life prediction algorithm where a model of the degradation process is suggested. This preliminary remaining life prediction algorithm serves as a demonstration of how prognostics methodologies could be used for electrolytic capacitors. In addition, the use degradation progression data from accelerated aging, provides an avenue for validation of applications of the Kalman filter based prognostics methods typically used for remaining useful life predictions in other applications.

  7. Preparation and characterization of plasticized high molecular weight PVC-based polymer electrolytes

    Indian Academy of Sciences (India)

    S Ramesh; Geok Bee Teh; Rong-Fuh Louh; Yong Kong Hou; Pung Yen Sin; Lim Jing Yi

    2010-02-01

    Poly(vinyl chloride) (PVC)-based polymer electrolytes films consisting of lithium trifluromethanesulfonate (LiCF3SO3)-ethylene carbonate (EC) were prepared by the solution-casting method. Ionic conductivities of the electrolytes have been determined by an impedance studies in the temperature range of 298–373 K. Complexation of the prepared electrolytes is studied by X-ray diffraction (XRD) analysis. Thermogravimetric analysis (TGA) was used to confirm the thermal stability of the polymer electrolytes. The conductivity–temperature plots were found to follow an Arrhenius nature. All these films are found to be thermally stable until 132–167°C.

  8. A flexible Li polymer primary cell with a novel gel electrolyte based on poly(acrylonitrile)

    Science.gov (United States)

    Akashi, Hiroyuki; Tanaka, Ko-ichi; Sekai, Koji

    The performance of a Li polymer primary cell with fire-retardant poly(acrylonitrile) (PAN)-based gel electrolytes is reported. By optimizing electrodes, electrolytes, the packaging material, and the structural design of the polymer cell, we succeeded in developing a "film-like" Li polymer primary cell with sufficient performance for practical use. The cell is flexible and less than 0.5 mm thick, which makes it suitable for a power source for some smart devices, such as an IC card. Fast cation conduction in the gel electrolyte minimizes the drop of the discharge capacity even at -20 °C. The high chemical stability of the gel electrolytes and the new packaging material allow the self-discharge rate to be limited to under 4.3%, which is equivalent to that of conventional coin-shaped or cylindrical Li-MnO 2 cells.

  9. H2O2 detection analysis of oxygen reduction reaction on cathode and anode catalysts for polymer electrolyte fuel cells

    Science.gov (United States)

    Kishi, Akira; Shironita, Sayoko; Umeda, Minoru

    2012-01-01

    The generation percentage of H2O2 during oxygen reduction reaction (ORR) at practical powder electrocatalysts was evaluated using a scanning electrochemical microscope (SECM). We employed a porous microelectrode that contains electrocatalysts, namely, Pt/C, Pt-Co/C, and Pt-Ru/C as the oxygen reduction electrode of the SECM, and the Pt microelectrode was used as the H2O2 detector. First, the H2O2 generation amount at Pt/Cs was measured by changing the Pt loading amount. A Pt/C with a higher Pt loading has a higher ORR activity and generates a larger amount of H2O2. However, the percentage of H2O2 generated with respect to the ORR is the same regardless of the Pt loading amount. Next, H2O2 generation is markedly suppressed at the Pt-Co/C and Pt-Ru/C in the potential ranges of practical fuel cell cathode and anode, respectively. This explains that the Pt-Co/C is effective when used as a cathode, and the anode Pt-Ru/C enables the reduction of the H2O2 generation even if O2 crossleak occurs in the practical polymer electrolyte fuel cell.

  10. A Synopsis of Interfacial Phenomena in Lithium-Based Polymer Electrolyte Electrochemical Cells

    Science.gov (United States)

    Baldwin, Richard S.; Bennett, William R.

    2007-01-01

    The interfacial regions between electrode materials, electrolytes and other cell components play key roles in the overall performance of lithium-based batteries. For cell chemistries employing lithium metal, lithium alloy or carbonaceous materials (i.e., lithium-ion cells) as anode materials, a "solid electrolyte interphase" (SEI) layer forms at the anode/electrolyte interface, and the properties of this "passivating" layer significantly affect the practical cell/battery quality and performance. A thin, ionically-conducting SEI on the electrode surface can beneficially reduce or eliminate undesirable side reactions between the electrode and the electrolyte, which can result in a degradation in cell performance. The properties and phenomena attributable to the interfacial regions existing at both anode and cathode surfaces can be characterized to a large extent by electrochemical impedance spectroscopy (EIS) and related techniques. The intention of the review herewith is to support the future development of lithium-based polymer electrolytes by providing a synopsis of interfacial phenomena that is associated with cell chemistries employing either lithium metal or carbonaceous "composite" electrode structures which are interfaced with polymer electrolytes (i.e., "solvent-free" as well as "plasticized" polymer-binary salt complexes and single ion-conducting polyelectrolytes). Potential approaches to overcoming poor cell performance attributable to interfacial effects are discussed.

  11. Kinetic factors determining conducting filament formation in solid polymer electrolyte based planar devices

    Science.gov (United States)

    Krishnan, Karthik; Aono, Masakazu; Tsuruoka, Tohru

    2016-07-01

    Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength, and the reduction sites for precipitation. Different filament formations, resulting from unidirectional and dendritic growth behaviours, can be controlled by tuning specified parameters, which in turn improves the stability and performance of SPE-based devices.Resistive switching characteristics and conducting filament formation dynamics in solid polymer electrolyte (SPE) based planar-type atomic switches, with opposing active Ag and inert Pt electrodes, have been investigated by optimizing the device configuration and experimental parameters such as the gap distance between the electrodes, the salt inclusion in the polymer matrix, and the compliance current applied in current-voltage measurements. The high ionic conductivities of SPE enabled us to make scanning electron microscopy observations of the filament formation processes in the sub-micrometer to micrometer ranges. It was found that switching behaviour and filament growth morphology depend strongly on several kinetic factors, such as the redox reaction rate at the electrode-polymer interfaces, ion mobility in the polymer matrix, electric field strength

  12. Tin Coatings Electrodeposited from Sulfonic Acid-Based Electrolytes: Tribological Behavior

    Science.gov (United States)

    Bengoa, L. N.; Tuckart, W. R.; Zabala, N.; Prieto, G.; Egli, W. A.

    2015-06-01

    A high efficiency methane sulfonic acid electrolyte used for tin electrodeposition was studied, and the properties of the resulting deposits were compared to those of tin coatings obtained from an industrial phenol sulfonic acid electrolyte. Cyclic voltammetry was used to study the effect of organic additives on the reduction process to define the composition of the electrolytic bath. Thick tin electrodeposits were obtained on rotating cylinder steel electrodes, and their surface morphology, preferred crystal orientation, surface roughness, micro hardness, and tribological behavior were measured. Smooth, adherent, and bright tin coatings were obtained from the methane sulfonic acid electrolyte, which differed in morphology and texture from tin electrodeposited from the industrial bath. Influence of organic additives on preferred crystal orientation of the coatings was found to be stronger than changing the supporting sulfonic acid type. Tribological tests showed that the two types of deposits have a similar coefficient of friction. However, tin coatings obtained from methane sulfonic electrolytes presented a lower wear resistance and underwent galling at lower loads.

  13. Studies on the enhancement of solid electrolyte interphase formation on graphitized anodes in LiX-carbonate based electrolytes using Lewis acid additives for lithium-ion batteries

    Science.gov (United States)

    Li, L. F.; Xie, B.; Lee, H. S.; Li, H.; Yang, X. Q.; McBreen, J.; Huang, X. J.

    The new electrolyte systems utilizing one type of Lewis acids, the boron based anion receptors (BBARs) with LiF, Li 2O, or Li 2O 2 in carbonate solutions have been developed and reported by us. These systems open up a new approach in developing non-aqueous electrolytes with higher operating voltage and less moisture sensitivity for lithium-ion batteries. However, the formation of a stable solid electrolyte interphase (SEI) layer on the graphitized anodes is a serious problem needs to be solved for these new electrolyte systems, especially when propylene carbonate (PC) is used as a co-solvent. Using lithium bis(oxalato)borate (LiBOB) as an additives, the SEI layer formation on mesophase carbon microbeads (MCMB) anode is significantly enhanced in these new electrolytes containing boron-based anion receptors, such as tris(pentafluorophenyl) borane, and lithium salt such as LiF, or lithium oxides such as Li 2O or Li 2O 2 in PC and dimethyl carbonate (DMC) solvents. The cells using these electrolytes and MCMB anodes cycled very well and the PC co-intercalation was suppressed. Fourier transform infrared spectroscopy (FTIR) studies show that one of the electrochemical decomposition products of LiBOB, lithium carbonate (Li 2CO 3), plays a quite important role in the stablizing SEI layer formation.

  14. Performance enhancement of phosphoric acid fuel cell using phosphosilicate gel based electrolyte

    Institute of Scientific and Technical Information of China (English)

    Kajari Kargupta; Swati Saha; Dipali Banerjee; Mrinal Seal; Saibal Ganguly

    2012-01-01

    Replacement of phosphoric acid electrolyte by phosphosilicate gel based electrolytes is proposed for performance enhancement of phosphoric acid fuel cell (PAFG).Phosphosilicate gel in paste form and in powder form is synthesized from tetraethoxysilane and orthophosphoric acid using sol-gel method for two different P/Si ratio of 5 and 1.5 respectively.Replacement of phosphoric acid electrolyte by phosphosilicate gel paste enhances the peak power generation of the fuel cell by 133% at 120 ℃ cell temperature; increases the voltage generation in the ohmic regime and extends the maximum possible load current.Polyinyl alcohol (PVA) is used to bind the phosphosilicate gel powder and to form the hybrid crosslinked gel polymer electrolyte membrane.Soaking the membrane with phosphoric acid solution,instead of that with water improves the proton conductivity of the membrane,enhances the voltage and power generation by the fuel cell and extends the maximum possible operating temperature.At lower operating temperature of 70 ℃,peak power produced by phosphosilicate gel polymer electrolyte membrane fuel cell ( PGMFC ) is increased by 40% compared to that generated by phosphoric acid fuel cell ( PAFC ).However,the performance of composite membrane diminishes as the cell temperature increases.Thus phosphosilicate gel in paste form is found to be a good alternative of phosphoric acid electrolyte at medium operating temperature range while phosphosilicate gel-PVA composite offers performance enhancement at low operating temperatures.

  15. A Catalytic Path for Electrolyte Reduction in Lithium-Ion Cells Revealed by in Situ Attenuated Total Reflection-Fourier Transform Infrared Spectroscopy

    KAUST Repository

    Shi, Feifei

    2015-03-11

    © 2015 American Chemical Society. Although controlling the interfacial chemistry of electrodes in Li-ion batteries (LIBs) is crucial for maintaining the reversibility, electrolyte decomposition has not been fully understood. In this study, electrolyte decomposition on model electrode surfaces (Au and Sn) was investigated by in situ attenuated total reflection-Fourier transform infrared (ATR-FTIR) spectroscopy. Simultaneously obtained ATR-FTIR spectra and cyclic voltammetry measurements show that lithium ethylene dicarbonate and lithium propionate form on the Au electrode at 0.6 V, whereas diethyl 2,5-dioxahexane dicarboxylate and lithium propionate form on the Sn electrode surface at 1.25 V. A noncatalytic reduction path on the Au surface and a catalytic reduction path on the Sn surface are introduced to explain the surface dependence of the overpotential and product selectivity. This represents a new concept for explaining electrolyte reactions on the anode of LIBs. The present investigation shows that catalysis plays a dominant role in the electrolyte decomposition process and has important implications in electrode surface modification and electrolyte recipe selection, which are critical factors for enhancing the efficiency, durability, and reliability of LIBs.

  16. Application of polyacrylonitrile-based polymer electrolytes in rechargeable lithium batteries

    DEFF Research Database (Denmark)

    Perera, K.S.; Dissanayake, M.A.K.L.; Skaarup, Steen;

    2008-01-01

    Polyacrylonitrile (PAN)-based polymer electrolytes have obtained considerable attention due to their fascinating characteristics such as appreciable ionic conductivity at ambient temperatures and mechanical stability. This study is based on the system PAN-ethylene carbonate (EC)-propylene carbonate...

  17. The Effect of Titania-coating on Electrochemical Characteristics of CMS in PC-Based Electrolyte

    Institute of Scientific and Technical Information of China (English)

    J. Gao; L. C. Yang; T. Zhang; Y.P. Wu; H.Q. Wu

    2005-01-01

    @@ 1Introduction Lithium-ion batteries have been widely used in portable electronic devices due to their high voltage and high energy density. Most research has concentrated on improving their performance such as capacity, cycling characteristics and low temperature range. Propylene carbonate (PC)-based electrolytes are more desirable than ethylene carbonate (EC)-based electrolytes because of their low-temperature characteristics[1]. Unfortunately, PC is not used in commercial lithium-ion batteries because solvent decomposition and graphite exfoliation occur when lithium intercalates[2].

  18. Development of gas chromatographic methods for the analyses of organic carbonate-based electrolytes

    Science.gov (United States)

    Terborg, Lydia; Weber, Sascha; Passerini, Stefano; Winter, Martin; Karst, Uwe; Nowak, Sascha

    2014-01-01

    In this work, novel methods based on gas chromatography (GC) for the investigation of common organic carbonate-based electrolyte systems are presented, which are used in lithium ion batteries. The methods were developed for flame ionization detection (FID), mass spectrometric detection (MS). Further, headspace (HS) sampling for the investigation of solid samples like electrodes is reported. Limits of detection are reported for FID. Finally, the developed methods were applied to the electrolyte system of commercially available lithium ion batteries as well as on in-house assembled cells.

  19. Role of polyvinyl alcohol in the conductivity behaviour of polyethylene glycol-based composite gel electrolytes

    Indian Academy of Sciences (India)

    S K Patel; R B Patel; A Awadhia; N Chand; S L Agrawal

    2007-09-01

    An attempt has been made in the present work to combine gel and composite polymer electrolyte routes together to form a composite polymeric gel electrolyte that is expected to possess high ionic conductivity with good mechanical integrity. Polyethylene glycol (PEG) based composite gel electrolytes using polyvinyl alcohol (PVA) as guest polymer have been synthesized with 1 molar solution of ammonium thiocyanate (NH4SCN) in dimethyl sulphoxide (DMSO) and electrically characterized. The ionic conductivity measurements indicate that PEG : PVA : NH4SCN-based composite gel electrolytes are superior (max = 5.7 × 10−2 S cm-1) to pristine electrolytes (PEG : NH4SCN system) and conductivity variation with filler concentration remains within an order of magnitude. The observed conductivity maxima have been correlated to PEG : PVA : NH4SCN- and PVA : NH4SCN-type complexes. Temperature dependence of conductivity profiles exhibits Arrhenius behaviour in low temperature regime followed by VTF character at higher temperature.

  20. Properties of sodium-based ionic liquid electrolytes for sodium secondary battery applications

    International Nuclear Information System (INIS)

    The enormous demands on available global lithium resources have raised concerns about the sustainability of the supply of lithium. Sodium secondary batteries have emerged as promising alternatives to lithium batteries. We describe here sodium bis(trifluoromethylsulfonyl) amide (NaNTf2) electrolyte systems based on 1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl) amide (C4mpyrNTf2) ionic liquids. The electrochemical stability of the system was examined; a pair of facile cathodic and anodic processes around 0 V vs. Na/Na+ were observed in cyclic voltammetry measurements and interpreted as deposition and dissolution of sodium metal. Density, viscosity and conductivity of the electrolytes were studied. It was found that the ionic conductivity of electrolytes reached as high as 8 mS/cm, decreasing slowly as the salt content increased due to increasing of viscosity and density of the electrolyte. Therefore, sodium electrolytes based on C4mpyrNTf2 appear to be promising for secondary sodium battery applications

  1. Hydrogen ion conducting starch-chitosan blend based electrolyte for application in electrochemical devices

    International Nuclear Information System (INIS)

    Highlights: • Cation transference number of the highest conducting starch-chitosan-NH4Cl-glycerol electrolyte is 0.56. • LSV has shown that the polymer electrolyte is suitable for fabrication of EDLC and proton batteries. • The fabricated EDLC has been charged and discharged for 500 cycles. • Secondary proton battery has been charged and discharged for 40 cycles. - Abstract: This paper reports the characterization of starch-chitosan blend based solid polymer electrolyte (SPE) system and its application in electrochemical double layer capacitor (EDLC) and proton batteries. All the SPEs are prepared via solution cast technique. Results from X-ray diffraction (XRD) verify the conductivity result from our previous work. Scanning electron microscopy (SEM) analysis shows the difference in the electrolyte's surface with respect to NH4Cl and glycerol content. From transference number measurements (TNM), transference number of ion (tion) of the electrolytes shows that ion is the dominant conducting species. Transference number of cation (t+) for the highest conducting electrolyte is found to be 0.56. Linear sweep voltammetry (LSV) result confirms the suitability of the highest conducting electrolyte to be used in the fabrication of EDLC and proton batteries. The EDLC has been characterized using cyclic voltammetry (CV) and galvanostatic charge-discharge measurements. The open circuit potential (OCP) of the primary proton batteries for 48 h is lasted at (1.54 ± 0.02) V, while that of secondary proton batteries is lasted at (1.58 ± 0.01) V. The primary proton batteries have been discharged at different constant currents. The secondary proton battery has been charged and discharged for 40 cycles

  2. Electrospun hydrophilic fumed silica/polyacrylonitrile nanofiber-based composite electrolyte membranes

    Energy Technology Data Exchange (ETDEWEB)

    Jung, Hong-Ryun; Ju, Dong-Hyuk [Faculty of Applied Chemical Engineering, Chonnam National University, 300 Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of); Center for Functional Nano Fine Chemicals, Chonnam National University, 300 Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of); Lee, Wan-Jin [Faculty of Applied Chemical Engineering, Chonnam National University, 300 Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of); Center for Functional Nano Fine Chemicals, Chonnam National University, 300 Yongbong-dong, Buk-gu, Gwangju 500-757 (Korea, Republic of)], E-mail: wjlee@jnu.ac.kr; Zhang, Xiangwu; Kotek, Richard [Fiber and Polymer Science Program, Department of Textile Engineering, Chemistry and Science, North Carolina State University, Raleigh, NC 27695-8031 (United States)

    2009-05-01

    Hydrophilic fumed silica (SiO{sub 2})/polyacrylonitrile (PAN) composite electrolyte membranes were prepared by electrospinning composite solutions of SiO{sub 2} and PAN in N,N-dimethylformamide (DMF). Among electrospinning solutions with various SiO{sub 2} contents, the 12 wt% SiO{sub 2} in PAN solution has highest zeta potential (-40.82 mV), and exhibits the best dispersibility of SiO{sub 2} particles. The resultant 12 wt% SiO{sub 2}/PAN nanofiber membrane has the smallest average fiber diameter, highest porosity, and largest specific surface area. In addition, this membrane has a three-dimensional network structure, which is fully interconnected with combined mesopores and macropores because of a good SiO{sub 2} dispersion. Composite electrolyte membranes were prepared by soaking these porous nanofiber membranes in 1 M lithium hexafluorophosphate (LiPF{sub 6}) in ethylene carbonate (EC)/dimethyl carbonate (DMC) (1:1 vol%). It is found that 12 wt% SiO{sub 2}/PAN electrolyte membrane has the highest conductivity (1.1 x 10{sup -2} S cm{sup -1}) due to the large liquid electrolyte uptake (about 490%). In addition, the electrochemical performance of composite electrolyte membranes is also improved after the introduction of SiO{sub 2}. For initial cycle, 12 wt% SiO{sub 2}/PAN composite electrolyte membrane delivers the discharge capacity of 139 mAh g{sup -1} as 98% of theoretical value, and still retains a high value of 127 mAh g{sup -1} as 89% at 150th cycle, which is significantly higher that of pure PAN nanofiber-based electrolyte membranes.

  3. Lithium ion conducting solid polymer blend electrolyte based on bio-degradable polymers

    Indian Academy of Sciences (India)

    Natarajan Rajeswari; Subramanian Selvasekarapandian; Moni Prabu; Shunmugavel Karthikeyan; C Sanjeeviraja

    2013-04-01

    Lithium ion conducting polymer blend electrolyte films based on poly(vinyl alcohol) (PVA) and poly(vinyl pyrrolidone) (PVP) with different Mwt% of lithium nitrate (LiNO3) salt, using a solution cast technique, have been prepared. The polymer blend electrolyte has been characterized by XRD, FTIR, DSC and impedance analyses. The XRD study reveals the amorphous nature of the polymer electrolyte. The FTIR study confirms the complex formation between the polymer and salt. The shifts in g values of 70 PVA–30 PVP blend and 70 PVA–30 PVP with different Mwt% of LiNO3 electrolytes shown by DSC thermograms indicate an interaction between the polymer and the salt. The dependence of g and conductivity upon salt concentration has been discussed. The ion conductivity of the prepared polymer electrolyte has been found by a.c. impedance spectroscopic analysis. The PVA–PVP blend system with a composition of 70 wt% PVA: 30 wt% PVP exhibits the highest conductivity of 1.58 × 10-6 Scm-1 at room temperature. Polymer samples of 70 wt% PVA–30 wt% PVP blend with different molecular weight percentage of lithium nitrate with DMSO as solvent have been prepared and studied. High conductivity of 6.828 × 10-4 Scm-1 has been observed for the composition of 70 PVA:30 PVP:25 Mwt% of LiNO3 with low activation energy 0.2673 eV. The conductivity is found to increase with increase in temperature. The temperature dependent conductivity of the polymer electrolyte follows the Arrhenius relationship which shows hopping of ions in the polymer matrix. The relaxation parameters () and () of the complexes have been calculated by using loss tangent spectra. The mechanical properties of polymer blend electrolyte such as tensile strength, elongation and degree of swelling have been measured and the results are presented.

  4. Gel polymer electrolytes based on nanofibrous polyacrylonitrile–acrylate for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Dul-Sun [Department of Chemical and Biological Engineering, Research Institute for Green Energy Convergence Technology, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of); Woo, Jang Chang [Department of Textile Engineering, Inha University, 100 Inharo, Nam-gu Incheon 402-751 (Korea, Republic of); Youk, Ji Ho, E-mail: youk@inha.ac.kr [Department of Textile Engineering, Inha University, 100 Inharo, Nam-gu Incheon 402-751 (Korea, Republic of); Manuel, James [Department of Chemical and Biological Engineering, Research Institute for Green Energy Convergence Technology, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of); Ahn, Jou-Hyeon, E-mail: jhahn@gnu.ac.kr [Department of Chemical and Biological Engineering, Research Institute for Green Energy Convergence Technology, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of); Department of Materials Engineering and Convergence Technology, Gyeongsang National University, 900 Gajwa-dong, Jinju 660-701 (Korea, Republic of)

    2014-10-15

    Graphical abstract: - Highlights: • Nanofibrous polyacrylonitrile–acrylate membranes were prepared by electrospinning. • Trimethylolpropane triacrylate was used as a crosslinking agent of fibers. • The GPE based on PAN–acrylate (1/0.5) showed good electrochemical properties. - Abstract: Nanofibrous membranes for gel polymer electrolytes (GPEs) were prepared by electrospinning a mixture of polyacrylonitrile (PAN) and trimethylolpropane triacrylate (TMPTA) at weight ratios of 1/0.5 and 1/1. TMPTA is used to achieve crosslinking of fibers thereby improving mechanical strength. The average fiber diameters increased with increasing TMPTA concentration and the mechanical strength was also improved due to the enhanced crosslinking of fibers. GPEs based on electrospun membranes were prepared by soaking them in a liquid electrolyte of 1 M LiPF{sub 6} in ethylene carbonate (EC)/dimethyl carbonate (DMC) (1:1, v/v). The electrolyte uptake and ionic conductivity of GPEs based on PAN and PAN–acrylate (weight ratio; 1/1 and 1/0.5) were investigated. Ionic conductivity of GPEs based on PAN–acrylate was the highest for PAN/acrylate (1/0.5) due to the proper swelling of fibers and good affinity with liquid electrolyte. Both GPEs based on PAN and PAN–acrylate membranes show good oxidation stability, >5.0 V vs. Li/Li{sup +}. Cells with GPEs based on PAN–acrylate (1/0.5) showed remarkable cycle performance with high initial discharge capacity and low capacity fading.

  5. Performance of flexible capacitors based on polypyrrole/carbon fiber electrochemically prepared from various phosphate electrolytes

    Science.gov (United States)

    Yuan, Wei; Han, Gaoyi; Chang, Yunzhen; Li, Miaoyu; Xiao, Yaoming; Zhou, Haihan; Zhang, Ying; Li, Yanping

    2016-11-01

    In order to investigate the influence of electrolytes in electro-deposition solution on the capacitive properties of polypyrrole (PPy), we have chosen phosphoric acid, phosphate, hydrogen phosphate and dihydrogen phosphate as electrolyte in deposition solution respectively and electrochemically deposited PPy on carbon fibers (CFs) via galvanostatic method. The morphologies of the PPy/CFs samples have been characterized by scanning electron microscope. The specific capacitance of PPy/CFs samples has been evaluated in different electrolytes through three-electrode test system. The assembled flexible capacitors by using PPy/CFs as electrodes and H3PO4/polyvinyl alcohol as gel electrolyte have been systematically measured by cyclic voltammetry, galvanostatic charge/discharge and electrochemical impedance spectroscopy. The results show that the electrochemical capacitors based on PPy/CFs prepared from deposition solution containing NaH2PO4·2H2O electrolyte exhibit higher specific capacitance, flexibility and excellent stability (retaining 96.8% of initial capacitance after 13,000 cycles), and that three cells connected in series can power a light-emitting diode.

  6. Impedance studies of a green blend polymer electrolyte based on PVA and Aloe-vera

    Science.gov (United States)

    Selvalakshmi, S.; Mathavan, T.; Vijaya, N.; Selvasekarapandian, Premalatha, M.; Monisha, S.

    2016-05-01

    The development of polymer electrolyte materials for energy generating and energy storage devices is a challenge today. A new type of blended green electrolyte based on Poly-vinyl alcohol (PVA) and Aloe-vera has been prepared by solution casting technique. The blending of polymers may lead to the increase in stability due to one polymer portraying itself as a mechanical stiffener and the other as a gelled matrix supported by the other. The prepared blend electrolytes were subjected to Ac impedance studies. It has been found out that the polymer film in which 1 gm of PVA was dissolved in 40 ml of Aloe-vera extract exhibits highest conductivity and its value is 3.08 × 10-4 S cm-1.

  7. Ionic liquid based lithium battery electrolytes: charge carriers and interactions derived by density functional theory calculations.

    Science.gov (United States)

    Angenendt, Knut; Johansson, Patrik

    2011-06-23

    The solvation of lithium salts in ionic liquids (ILs) leads to the creation of a lithium ion carrying species quite different from those found in traditional nonaqueous lithium battery electrolytes. The most striking differences are that these species are composed only of ions and in general negatively charged. In many IL-based electrolytes, the dominant species are triplets, and the charge, stability, and size of the triplets have a large impact on the total ion conductivity, the lithium ion mobility, and also the lithium ion delivery at the electrode. As an inherent advantage, the triplets can be altered by selecting lithium salts and ionic liquids with different anions. Thus, within certain limits, the lithium ion carrying species can even be tailored toward distinct important properties for battery application. Here, we show by DFT calculations that the resulting charge carrying species from combinations of ionic liquids and lithium salts and also some resulting electrolyte properties can be predicted. PMID:21591707

  8. Polymer Electrolyte-Based Ambient Temperature Oxygen Microsensors for Environmental Monitoring

    Science.gov (United States)

    Hunter, Gary W.; Xu, Jennifer C.; Liu, Chung-Chiun

    2011-01-01

    An ambient temperature oxygen microsensor, based on a Nafion polymer electrolyte, has been developed and was microfabricated using thin-film technologies. A challenge in the operation of Nafion-based sensor systems is that the conductivity of Nafion film depends on the humidity in the film. Nafion film loses conductivity when the moisture content in the film is too low, which can affect sensor operation. The advancement here is the identification of a method to retain the operation of the Nafion films in lower humidity environments. Certain salts can hold water molecules in the Nafion film structure at room temperature. By mixing salts with the Nafion solution, water molecules can be homogeneously distributed in the Nafion film increasing the film s hydration to prevent Nafion film from being dried out in low-humidity environment. The presence of organics provides extra sites in the Nafion film to promote proton (H+) mobility and thus improving Nafion film conductivity and sensor performance. The fabrication of ambient temperature oxygen microsensors includes depositing basic electrodes using noble metals, and metal oxides layer on one of the electrode as a reference electrode. The use of noble metals for electrodes is due to their strong catalytic properties for oxygen reduction. A conducting polymer Nafion, doped with water-retaining components and extra sites facilitating proton movement, was used as the electrolyte material, making the design adequate for low humidity environment applications. The Nafion solution was coated on the electrodes and air-dried. The sensor operates at room temperature in potentiometric mode, which measures voltage differences between working and reference electrodes in different gases. Repeat able responses to 21-percent oxygen in nitrogen were achieved using nitrogen as a baseline gas. Detection of oxygen from 7 to 21 percent has also been demonstrated. The room-temperature oxygen micro sensor developed has extremely low power

  9. Electrochemical and solid state NMR characterization of composite PEO-based polymer electrolytes

    International Nuclear Information System (INIS)

    A comprehensive matrix of composite poly(ethyleneoxide) (PEO)-based solid-state electrolytes was developed in order to systematically study a number of variables and their impact upon the electrochemical properties of the resulting materials. The different parameters studied in the fabrication of these materials include: (i) the lithium electrolyte salt type, (ii) the ether oxygen to lithium ratio, (iii) the molecular weight of PEO, (iv) the type of ceramic additive used, either aluminum oxide (Al2O3), silicon oxide (SiO2), or titanium oxide (TiO2), (v) the particle size of the additives used, and (vi) the concentration of additive (wt.%). The standard lithium salt used for the preparation of these electrolytes was lithium trifluoromethanesulfonate (lithium triflate or LiSO3CF3), which served as the baseline electrolyte salt. Other lithium salts investigated include: lithium perchlorate (LiClO4) and lithium bis-trifluoromethanesulfonimide (LiN(SO2CF3)2). Conductivity measurements were performed for each electrolyte membrane over a wide temperature range (23-100 deg. C). In addition, cyclic voltammetry measurements were performed on selected PEO membranes as a function of temperature to determine the impact of various parameters upon the electrochemical stability. It was observed that the parameter that displayed the most significant effect upon the PEO-base polymer conductivity was the lithium salt type employed. The lithium triflate salt-containing PEO polymers demonstrated the best mechanical properties before and after heat treatment. Ceramic fillers also appear to enhance the mechanical properties of PEO polymer electrolytes at temperatures above the melting point of PEO (60-70 deg. C). In addition to investigating the electrochemical characteristics of the composite membrane, solid state 7Li NMR characterization was performed to study ionic mobility by measuring spectral line widths and lithium self-diffusion coefficients. It was determined that ceramic

  10. Solid-state electric double layer capacitors fabricated with plastic crystal based flexible gel polymer electrolytes: Effective role of electrolyte anions

    Energy Technology Data Exchange (ETDEWEB)

    Suleman, Mohd; Kumar, Yogesh; Hashmi, S.A., E-mail: sahashmi@physics.du.ac.in

    2015-08-01

    Flexible gel polymer electrolyte (GPE) thick films incorporated with solutions of lithium trifluoromethanesulfonate (Li-triflate or LiTf) and lithium bis trifluoromethane-sulfonimide (LiTFSI) in a plastic crystal succinonitrile (SN), entrapped in poly(vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP) have been prepared and characterized. The films have been used as electrolytes in the electrical double layer capacitors (EDLCs). Coconut-shell derived activated carbon with high specific surface area (∼2100 m{sup 2} g{sup −1}) and mixed (micro- and meso-) porosity has been used as EDLC electrodes. The structural, thermal, and electrochemical characterization of the GPEs have been performed using scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC), impedance measurements and cyclic voltammetry. The high ionic conductivity (∼10{sup −3} S cm{sup −1} at 25 °C), good electrochemical stability window (>4.0 V) and flexible nature of the free-standing films of GPEs show their competence in the fabrication of EDLCs. The EDLCs have been tested using electrochemical impedance spectroscopy, cyclic voltammetry, and charge–discharge studies. The EDLCs using LiTf based electrolyte have been found to give higher values of specific capacitance, specific energy, power density (240–280 F g{sup −1}, ∼39 Wh kg{sup −1} and ∼19 kW kg{sup −1}, respectively) than the EDLC cell with LiTFSI based gel electrolyte. EDLCs have been found to show stable performance for ∼10{sup 4} charge–discharge cycles. The comparative studies indicate the effective role of electrolyte anions on the capacitive performance of the solid-state EDLCs. - Graphical abstract: Display Omitted - Highlights: • Flexible EDLCs with succinonitrile based gel electrolyte membranes are reported. • Anionic size of salts in gel electrolytes plays important role on capacitive performance. • Li-triflate incorporated gel electrolyte shows better

  11. Solid-state electric double layer capacitors fabricated with plastic crystal based flexible gel polymer electrolytes: Effective role of electrolyte anions

    International Nuclear Information System (INIS)

    Flexible gel polymer electrolyte (GPE) thick films incorporated with solutions of lithium trifluoromethanesulfonate (Li-triflate or LiTf) and lithium bis trifluoromethane-sulfonimide (LiTFSI) in a plastic crystal succinonitrile (SN), entrapped in poly(vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP) have been prepared and characterized. The films have been used as electrolytes in the electrical double layer capacitors (EDLCs). Coconut-shell derived activated carbon with high specific surface area (∼2100 m2 g−1) and mixed (micro- and meso-) porosity has been used as EDLC electrodes. The structural, thermal, and electrochemical characterization of the GPEs have been performed using scanning electron microscopy (SEM), X-ray diffraction (XRD), differential scanning calorimetry (DSC), impedance measurements and cyclic voltammetry. The high ionic conductivity (∼10−3 S cm−1 at 25 °C), good electrochemical stability window (>4.0 V) and flexible nature of the free-standing films of GPEs show their competence in the fabrication of EDLCs. The EDLCs have been tested using electrochemical impedance spectroscopy, cyclic voltammetry, and charge–discharge studies. The EDLCs using LiTf based electrolyte have been found to give higher values of specific capacitance, specific energy, power density (240–280 F g−1, ∼39 Wh kg−1 and ∼19 kW kg−1, respectively) than the EDLC cell with LiTFSI based gel electrolyte. EDLCs have been found to show stable performance for ∼104 charge–discharge cycles. The comparative studies indicate the effective role of electrolyte anions on the capacitive performance of the solid-state EDLCs. - Graphical abstract: Display Omitted - Highlights: • Flexible EDLCs with succinonitrile based gel electrolyte membranes are reported. • Anionic size of salts in gel electrolytes plays important role on capacitive performance. • Li-triflate incorporated gel electrolyte shows better performance over LiTFSI-based gel. • Highest

  12. Synthesis and characterization of CuO nanoparticles using strong base electrolyte through electrochemical discharge process

    Indian Academy of Sciences (India)

    PURUSHOTTAM KUMAR SINGH; PANKAJ KUMAR; MANOWAR HUSSAIN; ALOK KUMAR DAS; GANESH CHANDRA NAYAK

    2016-04-01

    In the present study, cupric oxide (CuO) nanoparticles were synthesized by electrochemical discharge process using strong base electrolytes. The experiments were carried out separately using NaOH and KOH electrolytes.The mass output rate and the crystal size were obtained with variation of the rotation speed of magnetic stirrer for both types of electrolytes. The mass output rate of CuO nanoparticles increased with the increase in the speed of rotation, and, after an optimum speed, it started decreasing. However, the size of the particles reduced with the increase of the rotation speed. The crystal plane of the obtained CuO nanoparticles was similar for both the electrolytes whereas the yield of nanoparticles was higher in KOH as compared with NaOH under the sameexperiment conditions. In this set of experiments, the maximum output rates obtained were 21.66 mg h$^{−1}$ for NaOH and 24.66 mg h$^{−1}$ for KOH at 200 rpm for a single discharge arrangement. The average crystal size of CuO particles obtained was in the range of 13–18 nm for KOH electrolyte and 15–20 nm for NaOH electrolyte. Scanning electron microscopy images revealed that flower-like and caddice clew-shaped CuO nanocrystalline particles weresynthesized by the electrochemical discharge process. Fourier transform infrared spectrum showed that the CuO nanoparticles have a pure and monolithic phase. UV–vis–NIR spectroscopy was used to monitor oxidation course of Cu→CuO and the band gap energy was measured as 2 and 2.6 eV for CuO nanoparticle synthesized in NaOH and KOH solutions, respectively.

  13. Acid-base and electrolyte disorders in patients with diabetes mellitus

    Directory of Open Access Journals (Sweden)

    Nikolaos Sotirakopoulos

    2012-01-01

    Full Text Available Diabetes mellitus is the most common metabolic disorder in the community. The diabetics may suffer from acid-base and electrolyte disorders due to complications of diabetes mellitus and the medication they receive. In this study, acid-base and electrolyte disorders were evaluated among outpatient diabetics in our hospital. The study consisted of patients with diabetes mellitus who visited the hospital as outpatients between the period January 1, 2004 to December 31, 2006. The patients′ medical history, age and type of diabetes were noted, including whether they were taking diuretics and calcium channel blockers or not. Serum creatinine, proteins, sodium, potassium and chloride and blood gases were measured in all patients. Proteinuria was measured by 24-h urine collection. Two hundred and ten patients were divided in three groups based on the serum creatinine. Group A consisted of 114 patients that had serum creatinine 3.1 mg/dL. Of the 210 patients, 176 had an acid-base disorder. The most common disorder noted in group A was metabolic alkalosis. In groups B and C, the common disorders were metabolic acidosis and alkalosis, and metabolic acidosis, respectively. The most common electrolyte disorders were hypernatremia (especially in groups A and B, hyponatremia (group C and hyperkalemia (especially in groups B and C. It is concluded that: (a in diabetic outpatients, acid-base and electrolyte disorders occurred often even if the renal function is normal, (b the most common disorders are metabolic alkalosis and metabolic acidosis (the frequency increases with the deterioration of the renal function and (c the common electrolyte disorders are hypernatremia and hypokalemia.

  14. The study of electrical conductivity and diffusion behavior of water-based and ferro/ferricyanide-electrolyte-based alumina nanofluids.

    Science.gov (United States)

    Liu, Chang; Lee, Hyeonseok; Chang, Ya-Huei; Feng, Shien-Ping

    2016-05-01

    Nanofluids are liquids containing suspensions of solid nanoparticles and have attracted considerable attention because they undergo substantial mass transfer and have many potential applications in energy technologies. Most studies on nanofluids have used low-ionic-strength solutions, such as water and ethanol. However, very few studies have used high-ionic-strength solutions because the aggregation and sedimentation of nanoparticles cause a stability problem. In this study, a stable water-based alumina nanofluid was prepared using stirred bead milling and exhibits a high electrical conductivity of 2420 μS/cm at 23 °C and excellent stability after five severe freezing-melting cycles. We then developed a process for mixing the water-based nanofluid with a high-ionic-strength potassium ferro/ferricyanide electrolyte and sodium dodecyl sulfate by using stirred bead milling and ultrasonication, thus forming a stable electrolyte-based nanofluid. According to the rotating disk electrode study, the electrolyte-based alumina nanofluid exhibits an unusual increase in the limiting current at high angular velocities, resulting from a combination of local percolation behavior and shear-induced diffusion. The electrolyte-based alumina nanofluid was demonstrated in a possible thermogalvanic application, since it is considered to be an alternative electrolyte for thermal energy harvesters because of the increased electrical conductivity and confined value of thermal conductivity.

  15. A fuel cell operating between room temperature and 250 C based on a new phosphoric acid based composite electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Lan, Rong [Department of Chemistry, Heriot-Watt University, Edinburgh EH14 4AS (United Kingdom); Xu, Xiaoxiang; Irvine, John T.S. [School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST (United Kingdom); Tao, Shanwen [Department of Chemistry, Heriot-Watt University, Edinburgh EH14 4AS (United Kingdom); School of Chemistry, University of St Andrews, St Andrews, Fife KY16 9ST (United Kingdom)

    2010-10-15

    A phosphoric acid based composite material with core-shell microstructure has been developed to be used as a new electrolyte for fuel cells. A fuel cell based on this electrolyte can operate at room temperature indicating leaching of H{sub 3}PO{sub 4} with liquid water is insignificant at room temperature. This will help to improve the thermal cyclability of phosphoric acid based electrolyte to make it easier for practical use. The conductivity of this H{sub 3}PO{sub 4}-based electrolyte is stable at 250 C with addition of the hydrophilic inorganic compound BPO{sub 4} forming a core-shell microstructure which makes it possible to run a PAFC at a temperature above 200 C. The core-shell microstructure retains after the fuel cell measurements. A power density of 350 mW/cm{sup 2} for a H{sub 2}/O{sub 2} fuel cell has been achieved at 200 C. The increase in operating temperature does not have significant benefit to the performance of a H{sub 2}/O{sub 2} fuel cell. For the first time, a composite electrolyte material for phosphoric acid fuel cells which can operate in a wide range of temperature has been evaluated but certainly further investigation is required. (author)

  16. Mg(PF6)2-Based Electrolyte Systems: Understanding Electrolyte-Electrode Interactions for the Development of Mg-Ion Batteries.

    Science.gov (United States)

    Keyzer, Evan N; Glass, Hugh F J; Liu, Zigeng; Bayley, Paul M; Dutton, Siân E; Grey, Clare P; Wright, Dominic S

    2016-07-20

    Mg(PF6)2-based electrolytes for Mg-ion batteries have not received the same attention as the analogous LiPF6-based electrolytes used in most Li-ion cells owing to the perception that the PF6(-) anion decomposes on and passivates Mg electrodes. No synthesis of the Mg(PF6)2 salt has been reported, nor have its solutions been studied electrochemically. Here, we report the synthesis of the complex Mg(PF6)2(CH3CN)6 and its solution-state electrochemistry. Solutions of Mg(PF6)2(CH3CN)6 in CH3CN and CH3CN/THF mixtures exhibit high conductivities (up to 28 mS·cm(-1)) and electrochemical stability up to at least 4 V vs Mg on Al electrodes. Contrary to established perceptions, Mg electrodes are observed to remain electrochemically active when cycled in the presence of these Mg(PF6)2-based electrolytes, with no fluoride (i.e., MgF2) formed on the Mg surface. Stainless steel electrodes are found to corrode when cycled in the presence of Mg(PF6)2 solutions, but Al electrodes are passivated. The electrolytes have been used in a prototype Mg battery with a Mg anode and Chevrel (Mo3S4)-phase cathode. PMID:27359196

  17. Methyl phosphate formation as a major degradation mode of direct methanol fuel cells with phosphoric acid based electrolytes

    DEFF Research Database (Denmark)

    Aili, David; Vassiliev, Anton; Jensen, Jens Oluf;

    2015-01-01

    Phosphoric acid and phosphoric acid doped polymer membranes are widely used as electrolytes in hydrogen based fuel cells operating at elevated temperatures. Such electrolytes have been explored for direct oxidation of methanol to further increase the versatility of the systems, however...

  18. Phthaloylchitosan-Based Gel Polymer Electrolytes for Efficient Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    S. N. F. Yusuf

    2014-01-01

    Full Text Available Phthaloylchitosan-based gel polymer electrolytes were prepared with tetrapropylammonium iodide, Pr4NI, as the salt and optimized for conductivity. The electrolyte with the composition of 15.7 wt.% phthaloylchitosan, 31.7 wt.% ethylene carbonate (EC, 3.17 wt.% propylene carbonate (PC, 19.0 wt.% of Pr4NI, and 1.9 wt.% iodine exhibits the highest room temperature ionic conductivity of 5.27 × 10−3 S cm−1. The dye-sensitized solar cell (DSSC fabricated with this electrolyte exhibits an efficiency of 3.5% with JSC of 7.38 mA cm−2, VOC of 0.72 V, and fill factor of 0.66. When various amounts of lithium iodide (LiI were added to the optimized gel electrolyte, the overall conductivity is observed to decrease. However, the efficiency of the DSSC increases to a maximum value of 3.71% when salt ratio of Pr4NI : LiI is 2 : 1. This cell has JSC, VOC and fill factor of 7.25 mA cm−2, 0.77 V and 0.67, respectively.

  19. Study on reduction of neptunium and uranium in nitric acid solution using flow type electrolytic cell, as a basic technique for advanced reprocessing process

    International Nuclear Information System (INIS)

    The reduction of neptunium and uranium was studied using a flow type electrolytic cell containing a carbon-fiber column electrode. Np(VI) (10-3 mol·l-1) in 3 mol·l-1 HNO3 solution was quantitatively reduced into Np(V) at the potential of 0.3 V vs. Ag/AgCl using the cell. Reduction of U(VI) (0.1 mol·l-1) into U(IV) with co-existing Np and Tc at -0.3 V vs. Ag/AgCl in 6 mol·l-1 HNO3 solution was also demonstrated. (author)

  20. New Insight into the Interaction between Carbonate-based Electrolyte and Cuprous Sulfide Electrode Material for Lithium Ion Batteries

    International Nuclear Information System (INIS)

    Cuprous sulfide (Cu2S) is attractive electrode material for lithium-ion battery because of its high capacity and energy density. Interestingly, the cycling stability of cuprous sulfide is poor in the carbonate-based electrolytes used in lithium ion battery industry but excellent in ether-based electrolyte. In this study, we have compared the electrochemical performance of commercially available cuprous sulfide in various kinds of carbonate-based electrolytes. Our results show that the specific capacity of Cu2S electrode fades quickly in cyclic carbonate-based electrolytes, but a much better electrochemical performance in linear carbonate-based electrolytes. In linear carbonate-based electrolyte (1 M LiPF6 in EMC), it exhibits a specific discharge capacity of 242.8 mAh g−1 after 50 cycles with coulombic efficiency of 99.6%. Our study suggests that the poor cycling performance of Cu2S in cyclic carbonate-based electrolytes is mainly due to the higher reactivity of cyclic carbonates with polysulfides on the surface of the electrode than linear carbonates, which was confirmed for the first time by our experiment studies and theoretical calculation

  1. Elucidating the Higher Stability of Vanadium (V) Cations in Mixed Acid Based Redox Flow Battery Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Vijayakumar, M.; Wang, Wei; Nie, Zimin; Sprenkle, Vincent L.; Hu, Jian Z.

    2013-11-01

    The Vanadium (V) cation structures in mixed acid based electrolyte solution were analysed by density functional theory (DFT) based computational modelling and 51V and 35Cl Nuclear Magnetic Resonance (NMR) spectroscopy. The Vanadium (V) cation exists as di-nuclear [V2O3Cl2.6H2O]2+ compound at higher vanadium concentrations (≥1.75M). In particular, at high temperatures (>295K) this di-nuclear compound undergoes ligand exchange process with nearby solvent chlorine molecule and forms chlorine bonded [V2O3Cl2.6H2O]2+ compound. This chlorine bonded [V2O3Cl2.6H2O]2+ compound might be resistant to the de-protonation reaction which is the initial step in the precipitation reaction in Vanadium based electrolyte solutions. The combined theoretical and experimental approach reveals that formation of chlorine bonded [V2O3Cl2.6H2O]2+ compound might be central to the observed higher thermal stability of mixed acid based Vanadium (V) electrolyte solutions.

  2. Effective solid electrolyte based on benzothiazolium for dye-sensitized solar cells.

    Science.gov (United States)

    Han, Lu; Wang, Ye Feng; Zeng, Jing Hui

    2014-12-24

    Thiaozole/benzothiaozole-based dicationic conductors were synthesized and applied as solid-state electrolyte in dye-sensitized solar cells (DSSCs). X-ray diffraction, scanning electron microscopy, thermal gravimetric analysis, steady-state voltammogram, photocurrent intensity-photovoltage test, and electrochemical impedance spectroscopy are used to characterize the materials and the mechanism of the cell performance. Compared to the traditional monocationic crystals, the dicationic crystals have a larger size and can provide more opportunities to fine-tune their physical/chemical properties. As a consequence, this solid-state electrolyte-based DSSC achieved photoelectric conversion efficiency of 7.90% under full air-mass (AM 1.5) sunlight (100 mW·cm(-2)).

  3. Characterization of ι-carrageenan and its derivative based green polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Jumaah, Fatihah Najirah; Mobaraka, Nadhratun Naiim; Ahmad, Azizan; Ramli, Nazaruddin [School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor Darul Ehsan (Malaysia)

    2013-11-27

    The new types of green polymer electrolytes based on ι-carrageenan derivative have been prepared. ι-carrageenan act as precursor was reacted with monochloroacetic acid to produce carboxymethyl ι-carrageenan. The powders were characterized by Attenuated Total Reflection Fourier Transform infrared (ATR-FTIR) spectroscopy and {sup 1}H nuclear magnetic resonance (NMR) to confirm the substitution of targeted functional group in ι-carrageenan. The green polymer electrolyte based on ι-carrageenan and carboxymethyl ι-carrageenan was prepared by solution-casting technique. The films were characterized by electrochemical impedance spectroscopy to determine the ionic conductivity. The ionic conductivity ι-carrageenan film were higher than carboxymethyl ι-carrageenan which 4.87 ×10{sup −6} S cm{sup −1} and 2.19 ×10{sup −8} S cm{sup −1}, respectively.

  4. Differential geometry-based solvation and electrolyte transport models for biomolecular modeling: a review

    OpenAIRE

    Wei, Guo Wei; Baker, Nathan A.

    2014-01-01

    This chapter reviews the differential geometry-based solvation and electrolyte transport for biomolecular solvation that have been developed over the past decade. A key component of these methods is the differential geometry of surfaces theory, as applied to the solvent-solute boundary. In these approaches, the solvent-solute boundary is determined by a variational principle that determines the major physical observables of interest, for example, biomolecular surface area, enclosed volume, el...

  5. Characteristics of tetrahydrofuran-based electrolytes with magnesium alkoxide additives for rechargeable magnesium batteries

    Science.gov (United States)

    Kim, In-Tae; Yamabuki, Kazuhiro; Sumimoto, Michinori; Tsutsumi, Hiromori; Morita, Masayuki; Yoshimoto, Nobuko

    2016-08-01

    The electrochemical behavior of magnesium (Mg) metal was investigated in tetrahydrofuran (THF)-based solutions containing magnesium bromide (MgBr2) and/or magnesium ethoxide (Mg(OEt)2). THF solutions containing a single solute, MgBr2 or Mg(OEt)2, show no visible faradaic current based on Mg deposition and/or dissolution. However, the electrolyte system containing both solutes, MgBr2 + Mg(OEt)2/THF, gives a reversible current response of Mg deposition and dissolution. The ionic structure of the electrolyte system containing the binary solute was examined by infrared (IR) spectroscopy and density functional theory (DFT) calculations. It was confirmed that MgBr2 and Mg(OEt)2 are coordinated (solvated) with THF molecules to form an EtOsbnd Mgsbnd Br·4THF complex. The DFT calculations also suggest the possible formation of μ-complexes for the MgBr2/Mg(OEt)2 binary system in THF. The voltammetric responses at the Pt electrode indicate low overpotential and high coulombic efficiency for Mg deposition and dissolution in THF-based solutions containing suitable molar ratios of MgBr2 and Mg(OEt)2. The constant-current charge-discharge cycling of Mg in MgBr2 + Mg(OEt)2/THF electrolyte also shows low overpotential and good cyclability over 300 cycles.

  6. Perfluoro anion based binary and ternary ionic liquids as electrolytes for dye-sensitized solar cells

    Science.gov (United States)

    Lin, Hsi-Hsin; Peng, Jia-De; Suryanarayanan, V.; Velayutham, D.; Ho, Kuo-Chuan

    2016-04-01

    In this work, eight new ionic liquids (ILs) based on triethylammonium (TEA) or n-methylpiperidinium (NMP) cations and perfluoro carboxylate (PFC) anions having different carbon chain lengths are synthesized and their physico-chemical properties such as density, decomposition temperature, viscosity and conductivity are determined. Photovoltaic characteristics of dye-sensitized solar cells (DSSCs) with binary ionic liquids electrolytes, containing the mixture of the synthesized ILs and 1-methyl-3-propyl imidazolium iodide (PMII) (v/v = 35/65), are evaluated. Among the different ILs, solar cells containing NMP based ILs show higher VOC than that of TEA, whereas, higher JSC is noted for the DSSCs incorporated with the latter when compared to the former. Further, the photo-current of the DSSCs decreases with the increase of the carbon chain length of perfluoro carboxylate anionic group of ILs. The cell performance of the DSSC containing ternary ionic liquids-based electrolytes compose of NMP-2C/TEA-2C/PMII (v/v/v = 28/7/65) exhibits a JSC of 12.99 mA cm-2, a VOC of 639.0 mV, a FF of 0.72, and a cell efficiency of 6.01%. The extraordinary durability of the DSSC containing the above combination of electrolytes stored in dark at 50 °C is proved to be unfailing up to 1200 h.

  7. Fuel-Cell Electrolytes Based on Organosilica Hybrid Proton Conductors

    Science.gov (United States)

    Narayan, Sri R.; Yen, Shiao-Pin S.

    2008-01-01

    A new membrane composite material that combines an organosilica proton conductor with perfluorinated Nafion material to achieve good proton conductivity and high-temperature performance for membranes used for fuel cells in stationary, transportation, and portable applications has been developed. To achieve high proton conductivities of the order of 10(exp -1)S/cm over a wide range of temperatures, a composite membrane based on a new class of mesoporous, proton-conducting, hydrogen-bonded organosilica, used with Nafion, will allow for water retention and high proton conductivity over a wider range of temperatures than currently offered by Nafion alone. At the time of this reporting, this innovation is at the concept level. Some of the materials and processes investigated have shown good proton conductivity, but membranes have not yet been prepared and demonstrated.

  8. Oxygen reduction reaction catalyzed by platinum nanonetwork prepared by template free one step synthesis for polymer electrolyte membrane fuel cells

    International Nuclear Information System (INIS)

    Highlights: • Supportless Pt nanonetwork (Pt NN) synthesized by novel template free one step method as per our earlier reported procedure. • Electrocatalytic activity of Pt NN studied taking oxygen reduction reaction in acid medium. • Kinetic and thermodynamic parameters were deduced under hydrodynamic conditions. • ORR mechanistic pathway was proposed based on kinetic rate constants. • ADT analysis found enhanced stability (5000 cycles) for Pt NN than Pt NN/VC and reported Pt/C. - Abstract: The reduction reaction of molecular oxygen (ORR) was investigated using supportless Pt nanonetwork (Pt NN) electrocatalyst in sulfuric acid medium. Pt NN was prepared by template free borohydride reduction. The transmission electron microscope images revealed a network like nano-architecture having an average cluster size of 30 nm. The electrochemical characterization of supportless and Vulcan carbon supported Pt NN (Pt NN/VC) was carried out using rotating disc and ring disc electrodes at various temperatures. Kinetic and thermodynamic parameters were estimated under hydrodynamic conditions and compared with Pt NN/VC and reported Pt/C catalysts. The accelerated durability test revealed that supportless Pt NN is quite stable for 5000 potential cycles with 22% reduction in electrochemical surface area (ECSA). While the initial limiting current density has in fact increased by 11.6%, whereas Pt NN/VC suffered nearly 55% loss in ECSA and 13% loss in limiting current density confirming an enhanced stability of supportless Pt NN morphology for ORR compared to conventional Pt/C ORR catalysts in acid medium

  9. Oxygen reduction reaction catalyzed by platinum nanonetwork prepared by template free one step synthesis for polymer electrolyte membrane fuel cells

    Energy Technology Data Exchange (ETDEWEB)

    Narayanamoorthy, B. [Department of Chemistry, Faculty of Science, Sri Chandrasekharendra Saraswathi Viswa Mahavidyalaya (SCSVMV University), Enathur, Kanchipuram 631 561 (India); Kumar, B.V.V.S. Pavan; Eswaramoorthy, M. [Nanomaterials and Catalysis Lab, Chemistry and Physics of Materials Unit, Jawaharlal Nehru Centre for Advanced Scientific Research (JNCASR), Bangalore 560 064 (India); Balaji, S., E-mail: prof.balaji13@gmail.com [Department of Chemistry, Faculty of Science, Sri Chandrasekharendra Saraswathi Viswa Mahavidyalaya (SCSVMV University), Enathur, Kanchipuram 631 561 (India)

    2014-07-01

    Highlights: • Supportless Pt nanonetwork (Pt NN) synthesized by novel template free one step method as per our earlier reported procedure. • Electrocatalytic activity of Pt NN studied taking oxygen reduction reaction in acid medium. • Kinetic and thermodynamic parameters were deduced under hydrodynamic conditions. • ORR mechanistic pathway was proposed based on kinetic rate constants. • ADT analysis found enhanced stability (5000 cycles) for Pt NN than Pt NN/VC and reported Pt/C. - Abstract: The reduction reaction of molecular oxygen (ORR) was investigated using supportless Pt nanonetwork (Pt NN) electrocatalyst in sulfuric acid medium. Pt NN was prepared by template free borohydride reduction. The transmission electron microscope images revealed a network like nano-architecture having an average cluster size of 30 nm. The electrochemical characterization of supportless and Vulcan carbon supported Pt NN (Pt NN/VC) was carried out using rotating disc and ring disc electrodes at various temperatures. Kinetic and thermodynamic parameters were estimated under hydrodynamic conditions and compared with Pt NN/VC and reported Pt/C catalysts. The accelerated durability test revealed that supportless Pt NN is quite stable for 5000 potential cycles with 22% reduction in electrochemical surface area (ECSA). While the initial limiting current density has in fact increased by 11.6%, whereas Pt NN/VC suffered nearly 55% loss in ECSA and 13% loss in limiting current density confirming an enhanced stability of supportless Pt NN morphology for ORR compared to conventional Pt/C ORR catalysts in acid medium.

  10. Nanocrystals of zirconia- and ceria-based solid electrolytes: Syntheses and properties

    Directory of Open Access Journals (Sweden)

    Takahisa Omata, Yuji Goto and Shinya Otsuka-Yao-Matsuo

    2007-01-01

    Full Text Available Nano-effect on solid electrolytes that appears as a conductivity enhancement is expected as a way to develop or improve practical solid ionic devices, such as solid oxide fuel cells. Interfaces play a major role in the enhanced conductivity. Using nanocrystals (NCs as the starting material, the nanostructured materials containing many interfaces, i.e., grain boundaries, can be simply made by forming the NCs with successive sintering without grain growth. The past decade has seen significant advances in the syntheses of solid electrolyte NCs and understanding the nano-effects on the ionic conductivity. In the present paper, the syntheses of zirconia- and ceria-based NCs, which are important constituent materials of solid oxide fuel cells, and their grain size-dependent conductivity due to the nano-effect are briefly reviewed.

  11. Novel ceramic fuel cell using non-ceria-based composites as electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Li, Song [Institute of Materials and Technology, Dalian Maritime University, Dalian 116026 (China); Department of Chemical Engineering and Technology, Royal Institute of Technology (KTH), S-10044 Stockholm (Sweden); Wang, Xiaodi [Department of Chemical Engineering and Technology, Royal Institute of Technology (KTH), S-10044 Stockholm (Sweden); College of Material Science and Chemical Engineering, Harbin Engineering University, Harbin 161041 (China); Zhu, Bin [Department of Chemical Engineering and Technology, Royal Institute of Technology (KTH), S-10044 Stockholm (Sweden)

    2007-12-15

    A novel concept of ceramic or solid oxide fuel cell (SOFC) based on non-ceria-salt-composites electrolyte has been investigated. The fuel cell using LiAlO{sub 2}-carbonate (LiNaCO{sub 3}) as electrolyte exhibits excellent performances, when we used hydrogen and air as fuel and oxidant respectively, instead of molten carbonate fuel cells (MCFCs) environment. The maximum output power density can reach 466 mW/cm{sup 2} at 650 C and the discharging current keeps constant. The ion transport mechanics of the ceramic fuel cell were discussed. In the H{sub 2}/air atmosphere, the new fuel cell function should be performed only by proton or oxygen ion conduction, which differs essentially from the MCFC function, in which the CO{sub 3}{sup 2-} conduction dominates process. (author)

  12. Composite polymer electrolyte based on PEO/Pvdf-HFP with MWCNT for lithium battery applications

    Science.gov (United States)

    Pradeepa, P.; Edwinraj, S.; Sowmya, G.; Kalaiselvimary, J.; Selvakumar, K.; Prabhu, M. Ramesh

    2016-05-01

    In the present study PEO and PVdF-HFP blend based composite polymer electrolytes (CPEs) has been prepared by using Multi Walled Carbon Nanotube (MWCNT), in order to examine the filler addition effect on the electrochemical properties. The complexed nanocomposite polymer electrolytes were obtained in the form of dimensionally stable and free standing films by using solution casting technique. The electrochemical properties of CPEs were measured by the AC impedance method. From the ionic conductivity results, the CPE containing MWCNT 2wt% showed the highest ionic conductivity with an excellent thermal stability at room temperature. The dielectric loss curve s for the sample 6.25wt% PEO: 18.75 wt% PVdF-HFP: 2wt% MWCNT reveal the low frequency β relaxation peak pronounced at high temperature, and it may caused by side group dipoles.

  13. Obtention and evaluation of polyethylene-based solid polymer electrolyte membranes fro hydrogen production

    Science.gov (United States)

    Masson, J. P.; Molina, R.; Roth, E.; Gaussens, G.; Lemaire, F.

    The fabrication and testing of a polyethylene-based solid polymer electrolyte for use in hydrogen production by water electrolysis are discussed. The fabrication process involves the radiation grafting of styrene groups onto a polyethylene matrix, followed by the chemical sulphonation of the resulting polymer. The membrane produced has exhibited resistivities as low as 60 ohm cm for a 1-mm thickness, and other properties of the same order of magnitude as those of the commercially available but more expensive Nafion 014 membrane. Life tests carried out at a current density of 2 kA/sq m in single-cell modules with 10-sq cm active surface have revealed no noticeable degradation in membrane mechanical or electrical properties after 3000 hours for membranes reinforced by an organic polymer fabric. The development of an electrolyzer specifically designed for operation with a solid polymer electrolyte is currently under way.

  14. Studies of plastic crystal gel polymer electrolytes based on poly(vinylidene chloride-co-acrylonitrile)

    Science.gov (United States)

    Hambali, D.; Zainuddin, Z.; Supa'at, I.; Osman, Z.

    2016-02-01

    In this work, we have prepared systems of poly(vinylidene chloride-co-acrylonitrile) (PVdC-co-AN) based gel polymer electrolytes (GPEs) which are single plasticized-GPEs and double plasticized-GPEs. Both systems comprised plastic crystal succinonitrile SN to form plastic crystal gel polymer electrolyte (PGPE) films. The ionic conductivity of the PGPE films were analysed by means of a.c. impedance spectroscopy at room temperature as well as at the temperature range of 303 K to 353 K. The temperature dependence ionic conductivity was found to obey the VTF rule. To study the interactions among the constituents in the PGPEs, Fourier Transform Infrared Spectroscopy (FTIR) was carried out and hence, the complexation between them has also been confirmed.

  15. Conductivity and characterization of plasticized polymer electrolyte based on (polyacrylonitrile-b-polyethylene glycol) copolymer

    Energy Technology Data Exchange (ETDEWEB)

    Liang, Yu-Hao; Chen, Chuh-Yung [Department of Chemical Engineering, National Cheng-Kung University, Tainan 70148 (China); Wang, Cheng-Chien [Department of Chemical and Material Engineering, Southern Taiwan University, Tainan 710 (China)

    2007-10-25

    A block copolymer polyacrylonitrile-b-polyethylene glycol was synthesized by the macroinitiator method. The copolymer mixed with a plasticizer - propylene carbonate (PC) and LiClO{sub 4} to form plasticized polymer electrolytes. FT-IR spectra show that the lithium ion interacts with the groups that contain the un-bonded electrons. The results of FT-IR also indicate that the EO segment can improve the dissociation of lithium salt. The differential scanning calorimeter (DSC) used to study the thermal behaviors of different compositions. In this study, the conductivity increases with the content of PEG. Additionally, the plasticized polymer electrolyte based on the block copolymer has a good conductivity and can retain good mechanical strength. (author)

  16. DSC and conductivity studies on PVA based proton conducting gel electrolytes

    Indian Academy of Sciences (India)

    S L Agrawal; Arvind Awadhia

    2004-12-01

    An attempt has been made in the present work to prepare polyvinyl alcohol (PVA) based proton conducting gel electrolytes in ammonium thiocyanate (NH4SCN) solution and characterize them. DSC studies affirm the formation of gels along with the presence of partial complexes. The cole–cole plots exhibit maximum ionic conductivity (2.58 × 10-3 S cm-1) for gel samples containing 6 wt% of PVA. The conductivity of gel electrolytes exhibit liquid like nature at low polymer concentrations while the behaviour is seen to be affected by the formation of PVA–NH4SCN complexes upon increase in polymer content beyond 5 wt%. Temperature dependence of ionic conductivity exhibits VTF behaviour.

  17. Ionic transport in P(VdF–HFP)–PEO based novel microporous polymer electrolytes

    Indian Academy of Sciences (India)

    M Deka; A Kumar

    2009-12-01

    A novel microporous polymer electrolyte (MPE) comprising blends of poly(vinylidene fluoride-cohexafluoropropylene) [P(VdF–HFP)] and polyethylene oxide (PEO) was prepared by phase inversion technique. It was observed that addition of PEO improved the pore configuration, such as pore size, pore connectivity and porosity of P(VdF–HFP) based membranes. The room temperature ionic conductivity was significantly enhanced. The highest porosity of about 65% and ionic conductivity of about 7 × 10-4 S cm-1 was obtained when the weight ratio of PEO was 40%. The liquid electrolyte uptake was found to increase with increase in porosity and pore size. However, at higher weight ratio of PEO (> 40%) porosity, pore size and ionic conductivity was decreased. This descending trend with further increase of PEO weight ratio was attributed to conglomeration effect of PEO at the pores.

  18. NMR spectroscopy study of agar-based polymers electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Mattos, R.I.; Tambelli, C.E. [Universidade de Sao Paulo (USP), Pirassununga, SP (Brazil). Fac. de Zootecnia e Engenharia de Alimentos; Raphael, E. [Universidade Federal de Sao Joao del-Rey (UFSJ), MG (Brazil). Dept. de Ciencias Naturais; Silva, I.D.A.; Magon, C.J.; Donoso, J.P. [Universidade de Sao Paulo (IFSC/USP), Sao Carlos, SP (Brazil). Inst. de Fisica

    2012-07-01

    Full text: This communication presents the results of preparation and characterization of transparent films obtained from agar and acetic acid. The films were characterized by electrochemical impedance spectroscopy (EIS) and nuclear magnetic resonance (NMR). The film formed by agar (Sigma Aldrich) was dispersed in water and kept under stirring and heating at 100 deg C. Next, glycerol, formaldehyde and different quantities of acetic acid (25 and 50 wt%) were added to this solution. The obtained solution was placed on a glass plate and left to dry for 48 hours in oven at 50 deg C to obtain the films, which were kept under vacuum before characterization. The ionic conductivity of the films display an Arrhenius behavior with activation energy E{sub a} = 78 (25 wt% of acetic acid) and E{sub a} = 87 kJ/mol (50 wt% of acetic acid). The conductivity values were 3:0 X 10{sup -6} and 1:2 X 10{sup -4} S/cm at room temperature and 4:4 X 10{sup -4} and 1:5 X 10{sup -3}S/cm at 70 deg C, for the 25 and 50 wt% of acetic acid respectively. To investigate the mechanism of protonic conduction in the polymer proton conductor proton NMR measurements were performed in the temperature range 200-370 K. The {sup 1}H-NMR results exhibit the qualitative feature associated with the proton mobility, namely the presence of well defined {sup 1}H spin-lattice relaxation maxima at 300 K. Activation energy of the order of 40 kJ/mol was obtained from the {sup 1}H-NMR line narrowing data. The ionic conductivity of the film combined with their transparency, flexibility, homogeneity and good adhesion to the glasses or metals indicate that agar-based SPEs are promising materials for used on optoelectronic applications. (author)

  19. Functional Knowledge Representation Based on Problem Reduction

    Institute of Scientific and Technical Information of China (English)

    高济

    1992-01-01

    This paper proposes an approach for functional knowledge representation based on problem reuction,which represents the organization of problem-solving activities in two levels:reduction and reasoning.The former makes the functional plans for problem-solving while the latter constructs functional units, called handlers,for executing subproblems designated by these plans.This approach emphasizes that the representation of domain knowledge should be closely combined with(rather than separated from)its use,therefore provides a set of reasoning-level primitives to construct handlers and formulate the control strategies for executing them,As reduction-level primitives,handlers are used to construct handler-associative networks,which become the executable representation of problem-reduction graphs,in order to realize the problem-solving methods suited to domain features.Besides,handlers and their control slots can be used to focus the attention of knowledge acquisition and reasoning control.

  20. In-Depth Interfacial Chemistry and Reactivity Focused Investigation of Lithium-Imide- and Lithium-Imidazole-Based Electrolytes.

    Science.gov (United States)

    Eshetu, Gebrekidan Gebresilassie; Diemant, Thomas; Grugeon, Sylvie; Behm, R Jürgen; Laruelle, Stephane; Armand, Michel; Passerini, Stefano

    2016-06-29

    A comparative and in-depth investigation on the reactivity of various Li-based electrolytes and of the solid electrolyte interface (SEI) formed at graphite electrode is carried out using X-ray photoelectron spectroscopy (XPS), chemical simulation test, and differential scanning calorimetry (DSC). The electrolytes investigated include LiX (X = PF6, TFSI, TDI, FSI, and FTFSI), dissolved in EC-DMC. The reactivity and SEI nature of electrolytes containing the relatively new imide (LiFSI and LiFTFSI) and imidazole (LiTDI) salts are evaluated and compared to those of well-researched LiPF6(-) and LiTFSI-based electrolytes. The thermal reactivity of LixC6 in the various electrolytes is found to be in the order of LiFSI > LiTDI > LiTFSI > LiFTFSI > LiPF6 and LiFSI > LiFTFSI > LiPF6 > LiTFSI > LiTDI in terms of onset exothermic temperature and total heat generated, respectively. Surface and depth-profiling XPS analysis of the SEI formed with the diverse electrolyte formulations provide insight into the differences and similarities (composition, thickness, and evolution, etc.) emanating from the structure of the various salt anions. PMID:27299469

  1. Ionic Liquid-Based Polymer Electrolytes via Surfactant-Assisted Polymerization at the Plasma-Liquid Interface.

    Science.gov (United States)

    Tran, Quoc Chinh; Bui, Van-Tien; Dao, Van-Duong; Lee, Joong-Kee; Choi, Ho-Suk

    2016-06-29

    We first report an innovative method, which we refer to as interfacial liquid plasma polymerization, to chemically cross-link ionic liquids (ILs). By this method, a series of all-solid state, free-standing polymer electrolytes is successfully fabricated where ILs are used as building blocks and ethylene oxide-based surfactants are employed as an assisted-cross-linking agent. The thickness of the films is controlled by the plasma exposure time or the ratio of surfactant to ILs. The chemical structure and properties of the polymer electrolyte are characterized by scanning electron microscopy (SEM), Fourier transformation infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR) spectroscopy, X-ray photoelectron spectroscopy (XPS), differential scanning calorimetry (DSC), and electrochemical impedance spectroscopy (EIS). Importantly, the underlying polymerization mechanism of the cross-linked IL-based polymer electrolyte is studied to show that fluoroborate or halide anions of ILs together with the aid of a small amount of surfactants having ethylene oxide groups are necessary to form cross-linked network structures of the polymer electrolyte. The ionic conductivity of the obtained polymer electrolyte is 2.28 × 10(-3) S·cm(-1), which is a relatively high value for solid polymer electrolytes synthesized at room temperature. This study can serve as a cornerstone for developing all-solid state polymer electrolytes with promising properties for next-generation electrochemical devices.

  2. Electrolytic fixer.

    Science.gov (United States)

    Stevens

    1982-12-01

    Interest in the recovery of silver from radiographic film generates a need to understand the operating procedures of recovery units utilizing the electrolytic fixer principle. Tailing or terminal units and recirculation units using electrolysis are evaluated. Difficulties encountered in the number of Coulombs applied to a specific amount of fixer are discussed. Reduction of sulfiding as a result of electrolysis and variations in film volumes are noted. The quantity and quality of silver collected can be improved by being aware of alterations in chemical activity used in a silver recovery program.

  3. Synthesis and characterization of an electrolyte system based on a biodegradable polymer

    Directory of Open Access Journals (Sweden)

    K. Sownthari

    2013-06-01

    Full Text Available A polymer electrolyte system has been developed using a biodegradable polymer namely poly-ε-caprolactone (PCL in combination with zinc triflate [Zn(CF3SO32] in different weight percentages and characterized during this investigation. Free-standing thin films of varying compositions were prepared by solution casting technique. The successful doping of the polymer has been confirmed by means of Fourier transform infrared spectroscopy (FTIR by analyzing the carbonyl (C=O stretching region of the polymer. The maximum ionic conductivity obtained at room temperature (25°C was found to be 8.8x10–6 S/cm in the case of PCL complexed with 25 wt% Zn(CF3SO32 which is five orders of magnitude higher than that of the pure polymer host material. The increase in amorphous phase with an increase in salt concentration of the prepared polymer electrolyte has also been confirmed from the concordant results obtained from X-ray diffraction (XRD, differential scanning calorimetry (DSC and scanning electron microscopic (SEM analyses. Furthermore, the electrochemical stability window of the prepared polymer electrolyte was found to be 3.7 V. An electrochemical cell has been fabricated based on Zn/MnO2 electrode couple as an application area and its discharge characteristics were evaluated.

  4. Electrical transport study of potato starch-based electrolyte system-II

    Energy Technology Data Exchange (ETDEWEB)

    Tiwari, Tuhina; Kumar, Manindra [Department of Physics (Mahila Mahavidyalay), Banaras Hindu University, Varanasi (India); Srivastava, Neelam, E-mail: neelamsrivastava_bhu@yahoo.co.in [Department of Physics (Mahila Mahavidyalay), Banaras Hindu University, Varanasi (India); Srivastava, P.C. [Department of Physics, Banaras Hindu University, Varanasi (India)

    2014-03-15

    Highlights: • Cheap and bio-degradable polymer electrolyte. • High conductivity ∼ 9.59 × 10{sup −3} Scm{sup −1}. • Detailed ion dynamics stud. -- Abstract: Glutaraldehyde (GA) crosslinked potato starch, after mixing with sodium iodide (NaI), resulted in electrolyte film having conductivity (σ) ∼ 10{sup −3} S/cm and ionic transference number (t{sub ion}) ≥ 0.99. Out of two preparation mediums, namely methanol and acetone, methanol based electrolyte system seems to be better. Super-linear power law (SLPL) phenomenon is observed in MHz frequency range and both lattice site potential and coulomb cage potential due to neighboring mobile charge carriers seems to be responsible for existence of SLPL, and variation of power law exponent ‘n’ with salt concentration. These ion dynamics results are supported by dielectric data also. Estimated number of charge carriers ‘N’ and mobility ‘μ’ are discussed with reference to different variants (medium of preparation, plasticizer, and salt content). Material's conductivity strongly depends on humidity.

  5. PREPARATION AND ELECTROCHEMICAL CHARACTERISTICS OF POLYMER ELECTROLYTE MEMBRANES BASED ON SAN/PVDF-HFP BLENDS

    Institute of Scientific and Technical Information of China (English)

    Ding-guo Tang; Lu Qi; Yun-xiang Ci

    2006-01-01

    A copolymer of poly(acrylonitrile-co-styrene) (SAN) was synthesized via an emulsion polymerization method.Novel polymer electrolyte membranes cast from the blends of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP), SAN and fumed silica (SiO2) are microporous and can be used in polymer lithium-ion batteries. The membrane shows excellent characteristics such as high ionic conductivity and good mechanical strength when the mass ratio between SAN and PVDF-HFP and SiO2 is 3.5/31.5/5. The ionic conductivity of the membrane soaked in a liquid electrolyte of 1 mol/L LiPF6/EC/DMC/DEC is 4.9 × 10-3 Scm-1 at 25℃. The membrane is electrochemical stable up to 5.5 V versus Li+/Li in the liquid electrolyte. The influences of SiO2 content on the porosity and mechanical strength of the membranes were studied.Polymer lithium-ion batteries based on the membranes were assembled and their performances were also studied.

  6. A new nanocomposite polymer electrolyte based on poly(vinyl alcohol) incorporating hypergrafted nano-silica

    KAUST Repository

    Hu, Xian-Lei

    2012-01-01

    Solid-state nanocomposite polymer electrolytes based on poly(vinyl alcohol)(PVA) incorporating hyperbranched poly(amine-ester) (HBPAE) grafted nano-silica (denoted as SiO2-g-HBPAE) have been prepared and investigated. Through surface pretreatment of nanoparticles, followed by Michael-addition and a self-condensation process, hyperbranched poly(amine-ester) was directly polymerized from the surface of nano-silica. Then the hypergrafted nanoparticles were added to PVA matrix, and blended with lithium perchlorate via mold casting method to fabricate nanocomposite polymer electrolytes. By introducing hypergrafted nanoparticles, ionic conductivity of solid composite is improved significantly at the testing temperature. Hypergrafted nano-silica may act as solid plasticizer, promoting lithium salt dissociation in the matrix as well as improving segmental motion of matrix. In addition, tensile testing shows that such materials are soft and tough even at room temperature. From the dielectric spectra of nanocomposite polymer electrolyte as the function of temperature, it can be deduced that Arrhenius behavior appears depending on the content of hypergrafted nano-silica and concentration of lithium perchlorate. At a loading of 15 wt% hypergrafted nano-silica and 54 wt% lithium perchlorate, promising ionic conductivities of PVA nanocomposite polymer electrolyte are achieved, about 1.51 × 10 -4 S cm-1 at 25 °C and 1.36 × 10-3 S cm-1 at 100 °C. © The Royal Society of Chemistry.

  7. Plasma-based radar cross section reduction

    CERN Document Server

    Singh, Hema; Jha, Rakesh Mohan

    2016-01-01

    This book presents a comprehensive review of plasma-based stealth, covering the basics, methods, parametric analysis, and challenges towards the realization of the idea. The concealment of aircraft from radar sources, or stealth, is achieved through shaping, radar absorbing coatings, engineered materials, or plasma, etc. Plasma-based stealth is a radar cross section (RCS) reduction technique associated with the reflection and absorption of incident electromagnetic (EM) waves by the plasma layer surrounding the structure. A plasma cloud covering the aircraft may give rise to other signatures such as thermal, acoustic, infrared, or visual. Thus it is a matter of concern that the RCS reduction by plasma enhances its detectability due to other signatures. This needs a careful approach towards the plasma generation and its EM wave interaction. The book starts with the basics of EM wave interactions with plasma, briefly discuss the methods used to analyze the propagation characteristics of plasma, and its generatio...

  8. Characterization of new polyacrylonitrile-co-bis[2-(2-methoxyethoxy)ethyl]itaconate based gel polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Choi, B.K.; Kim, Y.W. [Dankook Univ., Seoul (Korea). Dept. of Applied Physics; Gong, M.S. [Dankook Univ., Seoul (Korea). Dept. of Chemistry; Ahn, S.H. [Battery Research Center, LG Chemical Ltd., Taejon (Korea)

    2001-07-01

    Since the gel polymer electrolytes based on polyacrylonitrile (PAN) host have not been sufficient to fulfil the requirements as a separator of current lithium polymer battery, a new polymer host copolymerized with PAN, polyacrylonitrile-co-bis[2-(2-methoxyethoxy)ethyl]itaconate (abbreviated as PANI), was synthesized in expectation of enhanced trapping ability of liquid electrolytes. Electrical, electrochemical, thermal and mechanical studies have been carried out on PAN and PANI blended gel polymer electrolytes, complexed with ethylene carbonate (EC) and {sup g}amma{sup -}butyrolactone (BL) containing LiClO{sub 4} salt. The addition of PANI as a host polymer in the PAN-based gel polymer electrolytes has beneficial effects such as higher ionic conductivity, better thermal and electrochemical stabilities and enhanced ability of trapping organic solvent, possibly due to ion chelating ability of itaconate unit, though it shows less mechanical rigidity caused by amorphization of the PAN matrix. (Author).

  9. Reduction of Oxygen Bound with Hemoglobin by Electrolytic Method Using Hydrogen Gas in Phosphate-buffered Solution

    Institute of Scientific and Technical Information of China (English)

    2002-01-01

    Hemoglobin(Hb) is important as an oxygen carrier.The trace amount of oxygen in Hb was reduced by an electrolytic method using hydrogen as an electron donor.The deoxygenated Hb(deoxyHb) was stable against heat treatment at 60 ℃ with little precipitant.This method is safe,fast,and would be of potential use for large scale purification of Hb.

  10. Detection of distributed static and dynamic loads with electrolyte-enabled distributed transducers in a polymer-based microfluidic device

    International Nuclear Information System (INIS)

    This paper reports on the use of electrolyte-enabled distributed transducers in a polymer-based microfluidic device for the detection of distributed static and dynamic loads. The core of the device is a polymer rectangular microstructure integrated with electrolyte-enabled distributed transducers. Distributed loads acting on the polymer microstructure are converted to different deflections along the microstructure length, which are further translated to electrical resistance changes by electrolyte-enabled distributed transducers. Owing to the great simplicity of the device configuration, a standard polymer-based fabrication process is employed to fabricate this device. With custom-built electronic circuits and custom LabVIEW programs, fabricated devices filled with two different electrolytes, 0.1 M NaCl electrolyte and 1-ethyl-3-methylimidazolium dicyanamide electrolyte, are characterized, demonstrating the capability of detecting distributed static and dynamic loads with a single device. As a result, the polymer-based microfluidic device presented in this paper is promising for offering the capability of detecting distributed static and dynamic loads in biomedical/surgical, manufacturing and robotics applications. (paper)

  11. Preparation of a Star Network PEG-based Gel Polymer Electrolyte and Its Application to Electrochromic Devices

    Institute of Scientific and Technical Information of China (English)

    GONG Yong-Feng; FU Xiang-Kai; ZHANG Shu-Peng; JIANG Qing-Long

    2007-01-01

    A star network polymer with a pentaerythritol core linking four PEG-block polymeric arms was synthesized,and its corresponding gel polymer electrolyte based on lithium perchlorate and plasticizers EC/PC with the character being colorless and highly transparent has been also prepared. The polymer host was characterized and confirmed to be of a star network and an amorphous structure by FTIR, 1H NMR and XRD studies. The polymer host hold good mechanical properties for pentaerythritol cross-linking. Maximum ionic conductivity of the prepared electrolyte showed that the thermal stability was up to at least 150 ℃. The gel polymer electrolyte was further evaluated in electrochromic devices fabricated by transparent PET-ITO and electrochromically active viologen derivative films, and its excellent performance promised the usage of the gel polymer electrolyte as ionic conductor material in electrochrornic devices.

  12. A green and environment-friendly gel polymer electrolyte with higher performances based on the natural matrix of lignin

    Science.gov (United States)

    Gong, Sheng-Dong; Huang, Yun; Cao, Hai-Jun; Lin, Yuan-Hua; Li, Yang; Tang, Shui-Hua; Wang, Ming-Shan; Li, Xing

    2016-03-01

    In order to explore one truly green and environment-friendly gel polymer electrolyte (GPE), the natural biopolymer of lignin is firstly all over the world used as matrix to prepare GPE. The electrolyte membrane based on lignin can be easily fabricated just with lignin, liquid electrolyte and distilled water. Through comprehensive investigation of obtained GPE, it is found that the liquid electrolyte uptake reaches up to 230 wt.%; before 100 °C, GPE does not lose any weight and is thermal stable; at room temperature the ion conductivity is 3.73 mS cm-1; the amazing property of lithium ion transference number is high up to 0.85; GPE expresses complete electrochemical stability before 7.5 V and favorable compatibility with lithium anode; the outstanding cell performance of C-rate and cycle capacity. All these remarkably excellent performances endow lignin with application potential in GPE used in lithium ion batteries (LIBs) with higher performances.

  13. An efficient dissipative particle dynamics-based algorithm for simulating electrolyte solutions

    CERN Document Server

    Medina, Stefan; Wang, Zhen-Gang; Schmid, Friederike

    2014-01-01

    We propose an efficient simulation algorithm based on the dissipative particle dynamics (DPD) method for studying electrohydrodynamic phenomena in electrolyte fluids. The fluid flow is mimicked with DPD particles while the evolution of the concentration of the ionic species is described using Brownian pseudo particles. The method is designed especially for systems with high salt concentrations, as explicit treatment of the salt ions becomes computationally expensive. For illustration, we apply the method to electro-osmotic flow over patterned, superhydrophobic surfaces. The results are in good agreement with recent theoretical predictions.

  14. Investigation of a novel ternary electrolyte based on dimethyl sulfite and lithium difluoromono(oxalato)borate for lithium ion batteries

    Science.gov (United States)

    Chen, Renjie; Zhu, Lu; Wu, Feng; Li, Li; Zhang, Rong; Chen, Shi

    2014-01-01

    Lithium difluoromono(oxalato)borate (LiODFB) has been used as a novel lithium salt for battery in recent studies. In this study, a series of novel electrolytes has been prepared by adding 30 vol% dimethyl sulfite (DMS) or dimethyl carbonate (DMC) as co-solvent into an ethylene carbonate (EC)/ethyl methyl carbonate (EMC) + LiX mixture, in which the LiX could be LiClO4, LiODFB, LiBOB, LiTFSI, or LiCF3SO3. These ternary electrolytes have been investigated for use in lithium ion batteries. FT-IR spectroscopy analysis shows that characteristic functional groups (-CO3, -SO3) undergo red-shift or blue-shift with the addition of different lithium salts. The LiODFB-EC/EMC/DMS electrolyte exhibits high ionic conductivity, which is mainly because of the low melting point of DMS, and LiODFB possessing high solubility. The Li/MCMB cells containing this novel electrolyte exhibit high capacities, good cycling performance, and excellent rate performance. These performances are probably because both LiODFB and DMS can assist in the formation of SEI films by reductive decomposition. Additionally, the discharge capacity of Li/LiCoO2 half cell containing LiODFB-EC/EMC/DMS electrolyte is 130.9 mAh g-1 after 50 cycles, and it is very comparable with the standard-commercial electrolyte. The results show that this study produces a promising electrolyte candidate for lithium ion batteries.

  15. Organosilicon-Based Electrolytes for Long-Life Lithium Primary Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Fenton, Kyle R. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Nagasubramanian, Ganesan [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Staiger, Chad L. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Pratt, III, Harry D. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Rempe, Susan B. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Leung, Kevin [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Chaudhari, Mangesh I. [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States); Anderson, Travis Mark [Sandia National Laboratories (SNL-NM), Albuquerque, NM (United States)

    2015-09-01

    This report describes advances in electrolytes for lithium primary battery systems. Electrolytes were synthesized that utilize organosilane materials that include anion binding agent functionality. Numerous materials were synthesized and tested in lithium carbon monofluoride battery systems for conductivity, impedance, and capacity. Resulting electrolytes were shown to be completely non-flammable and showed promise as co-solvents for electrolyte systems, due to low dielectric strength.

  16. Preparation and electrochemical characterization of polymer electrolytes based on electrospun poly(vinylidene fluoride-co-hexafluoropropylene)/polyacrylonitrile blend/composite membranes for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Raghavan, Prasanth; Zhao, Xiaohui; Shin, Chorong; Baek, Dong-Ho; Choi, Jae-Won; Manuel, James; Heo, Min-Yeong; Ahn, Jou-Hyeon [Department of Chemical and Biological Engineering and Engineering Research Institute, Gyeongsang National University, 900, Gajwa-dong, Jinju 660-701 (Korea); Nah, Changwoon [Department of Polymer-Nano Science and Technology, Chonbuk National University, 664-14, Duckjin-dong, Jeonju 561-756 (Korea)

    2010-09-15

    Apart from PEO based solid polymer electrolytes, tailor-made gel polymer electrolytes based on blend/composite membranes of poly(vinylidene fluoride-co-hexafluoropropylene) and polyacrylonitrile are prepared by electrospinning using 14 wt% polymer solution in dimethylformamide. The membranes show uniform morphology with an average fiber diameter of 320-490 nm, high porosity and electrolyte uptake. Polymer electrolytes are prepared by soaking the electrospun membranes in 1 M lithium hexafluorophosphate in ethylene carbonate/dimethyl carbonate. Temperature dependent ionic conductivity and their electrochemical performance are studied. The blend/composite polymer electrolytes show good ionic conductivity in the range of 10{sup -3}Scm{sup -1} at ambient temperature and good electrochemical performance. All the Polymer electrolytes show an anodic stability >4.6 V with stable interfacial resistance with storage time. The prototype cell shows good charge-discharge properties and stable cycle performance with comparable capacity fade compared to liquid electrolyte under the test conditions. (author)

  17. Electrochemical energy storage in montmorillonite K10 clay based composite as supercapacitor using ionic liquid electrolyte.

    Science.gov (United States)

    Maiti, Sandipan; Pramanik, Atin; Chattopadhyay, Shreyasi; De, Goutam; Mahanty, Sourindra

    2016-02-15

    Exploring new electrode materials is the key to realize high performance energy storage devices for effective utilization of renewable energy. Natural clays with layered structure and high surface area are prospective materials for electrical double layer capacitors (EDLC). In this work, a novel hybrid composite based on acid-leached montmorillonite (K10), multi-walled carbon nanotube (MWCNT) and manganese dioxide (MnO2) was prepared and its electrochemical properties were investigated by fabricating two-electrode asymmetric supercapacitor cells against activated carbon (AC) using 1.0M tetraethylammonium tetrafluroborate (Et4NBF4) in acetonitrile (AN) as electrolyte. The asymmetric supercapacitors, capable of operating in a wide potential window of 0.0-2.7V, showed a high energy density of 171Whkg(-1) at a power density of ∼1.98kWkg(-1). Such high EDLC performance could possibly be linked to the acid-base interaction of K10 through its surface hydroxyl groups with the tetraethylammonium cation [(C2H5)4N(+) or TEA(+)] of the ionic liquid electrolyte. Even at a very high power density of 96.4kWkg(-1), the cells could still deliver an energy density of 91.1Whkg(-1) exhibiting an outstanding rate capability. The present study demonstrates for the first time, the excellent potential of clay-based composites for high power energy storage device applications.

  18. Electrolytic reduction of a simulated oxide spent fuel and the fates of representative elements in a Li2O-LiCl molten salt

    Science.gov (United States)

    Park, Wooshin; Choi, Eun-Young; Kim, Sung-Wook; Jeon, Sang-Chae; Cho, Young-Hwan; Hur, Jin-Mok

    2016-08-01

    A series of electrolytic reduction experiments were carried out using a simulated oxide spent fuel to investigate the reduction behavior of elements in a mixed oxide condition and the fates of elements in the reduction process with 1.0 wt% Li2O-LiCl. It was found out that 155% of the theoretical charge was enough to reduce the simulated. Te and Eu were expected to possibly exist in the precipitate and on the anode surface, whereas Ba and Sr showed apparent dissolution behaviors. Rare earths showed relatively low metal fractions from 28.2 to 34.0% except for Y. And the solubility of rare earths was observed to be low due to the low concentration of Li2O. The reduction of U was successful as expected showing 99.8% of a metal fraction. Also it was shown that the reduction of ZrO2 would be effective when a relatively small amount was included in a metal oxide mixture.

  19. Towards A Model-Based Prognostics Methodology for Electrolytic Capacitors: A Case Study Based on Electrical Overstress Accelerated Aging

    Science.gov (United States)

    Celaya, Jose R.; Kulkarni, Chetan S.; Biswas, Gautam; Goebel, Kai

    2012-01-01

    A remaining useful life prediction methodology for electrolytic capacitors is presented. This methodology is based on the Kalman filter framework and an empirical degradation model. Electrolytic capacitors are used in several applications ranging from power supplies on critical avionics equipment to power drivers for electro-mechanical actuators. These devices are known for their comparatively low reliability and given their criticality in electronics subsystems they are a good candidate for component level prognostics and health management. Prognostics provides a way to assess remaining useful life of a capacitor based on its current state of health and its anticipated future usage and operational conditions. We present here also, experimental results of an accelerated aging test under electrical stresses. The data obtained in this test form the basis for a remaining life prediction algorithm where a model of the degradation process is suggested. This preliminary remaining life prediction algorithm serves as a demonstration of how prognostics methodologies could be used for electrolytic capacitors. In addition, the use degradation progression data from accelerated aging, provides an avenue for validation of applications of the Kalman filter based prognostics methods typically used for remaining useful life predictions in other applications.

  20. Flexible thin-film battery based on graphene-oxide embedded in solid polymer electrolyte

    Science.gov (United States)

    Kammoun, M.; Berg, S.; Ardebili, H.

    2015-10-01

    Enhanced safety of flexible batteries is an imperative objective due to the intimate interaction of such devices with human organs such as flexible batteries that are integrated with touch-screens or embedded in clothing or space suits. In this study, the fabrication and testing of a high performance thin-film Li-ion battery (LIB) is reported that is both flexible and relatively safer compared to the conventional electrolyte based batteries. The concept is facilitated by the use of solid polymer nanocomposite electrolyte, specifically, composed of polyethylene oxide (PEO) matrix and 1 wt% graphene oxide (GO) nanosheets. The flexible LIB exhibits a high maximum operating voltage of 4.9 V, high capacity of 0.13 mA h cm-2 and an energy density of 4.8 mW h cm-3. The battery is encapsulated using a simple lamination method that is economical and scalable. The laminated battery shows robust mechanical flexibility over 6000 bending cycles and excellent electrochemical performance in both flat and bent configurations. Finite element analysis (FEA) of the LIB provides critical insights into the evolution of mechanical stresses during lamination and bending.Enhanced safety of flexible batteries is an imperative objective due to the intimate interaction of such devices with human organs such as flexible batteries that are integrated with touch-screens or embedded in clothing or space suits. In this study, the fabrication and testing of a high performance thin-film Li-ion battery (LIB) is reported that is both flexible and relatively safer compared to the conventional electrolyte based batteries. The concept is facilitated by the use of solid polymer nanocomposite electrolyte, specifically, composed of polyethylene oxide (PEO) matrix and 1 wt% graphene oxide (GO) nanosheets. The flexible LIB exhibits a high maximum operating voltage of 4.9 V, high capacity of 0.13 mA h cm-2 and an energy density of 4.8 mW h cm-3. The battery is encapsulated using a simple lamination method

  1. Cobalt-Based Electrolytes for Dye-Sensitized Solar Cells: Recent Advances towards Stable Devices

    Directory of Open Access Journals (Sweden)

    Federico Bella

    2016-05-01

    Full Text Available Redox mediators based on cobalt complexes allowed dye-sensitized solar cells (DSCs to achieve efficiencies exceeding 14%, thus challenging the emerging class of perovskite solar cells. Unfortunately, cobalt-based electrolytes demonstrate much lower long-term stability trends if compared to the traditional iodide/triiodide redox couple. In view of the large-scale commercialization of cobalt-based DSCs, the scientific community has recently proposed various approaches and materials to increase the stability of these devices, which comprise gelling agents, crosslinked polymeric matrices and mixtures of solvents (including water. This review summarizes the most significant advances recently focused towards this direction, also suggesting some intriguing way to fabricate third-generation cobalt-based photoelectrochemical devices stable over time.

  2. Lithium/sulfur batteries with mixed liquid electrolytes based on ethyl 1,1,2,2-tetrafluoroethyl ether

    International Nuclear Information System (INIS)

    Highlights: • Electrolyte based on fluorinated ether of ETFE is used in Li/S battery. • ETFE improves cycling, rate and self-discharging performances of Li/S battery. • Surface film on Li anode modified by ETFE inhibits the shuttle of polysulfides. - Abstract: Fluorinated ether of ethyl 1,1,2,2-tetrafluoroethyl ether (ETFE) was selected as electrolyte solvent for lithium/sulfur battery, and the influence of ETFE in electrolyte on cell properties was first investigated. The enhanced stability of electrolyte/anode interface and improved electrochemical performances (cycling, rate and self-discharging) of the Li/S cell are presented by using ETFE-containing electrolyte, especially for complete replacement of tetraethylene glycol dimethyl ether (TEGDME) by ETFE in combine with 1,3-dioxolane (DOL). It is found that ETFE plays a key role in modifying the surface composition and structure of the metallic Li, forming a strengthened protective film on the anode during cycling. Besides, ETFE is considered to decrease the dissolution of polysulfides in the electrolyte. These factors together restrict the contact and reaction between polysulfides and Li anode

  3. A novel stability-enhanced lithium-oxygen battery with cellulose-based composite polymer gel as the electrolyte

    International Nuclear Information System (INIS)

    Highlights: • A novel cellulose-based composite polymer gel electrolyte (PGE) membrane is prepared. • PGE exhibits excellent ionic conductivity and electrochemical stability. • PEG reduces the penetration of oxygen to lithium anode and electrolyte loss. • Non-aqueous Li/O2 battery employing PGE membrane displays good cyclic stability. - Abstract: A novel lithium-oxygen (Li-O2) battery with a polymer gel electrolyte (PGE) membrane is successfully prepared. The membrane is a blend of cellulose acetate (CA) and poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) and is fabricated using a solution casting technique followed by impregnation with lithium bis(trifluoromethane sulfonimide) (LiTFSI) solution. We demonstrate that the PGE membrane has good electrolyte uptake and shows high ionic conductivity as well as excellent thermal and electrochemical stability. A Li-O2 battery containing our PGE as the electrolyte and separator exhibits good rate capability and enhanced cycling capacity retention compared to a battery using commercial liquid electrolyte and a polyethylene (PE) separator under the same conditions. We attribute this enhanced performance to the PGE, which maybe restrain the diffusion of oxygen from the air cathode to the Li metal anode. This study may prove valuable for resolving the problem of poor cycling stability in Li-O2 batteries caused by oxygen diffusion from cathode to anode

  4. Optimization of performances of gelatin/LiBF4-based polymer electrolytes by plasticizing effects

    International Nuclear Information System (INIS)

    Gelatin is a cheap and abundant natural product with very good biodegradation properties and can be used to obtain acetic acid or LiClO4-based gel polymer electrolytes (GPEs) with high ionic conductivity and good stability. This article presents results of GPEs obtained by the plasticization of gelatin and addition of LiBF4, where the optimization of the system was achieved by using a factorial design type 22 with two variables: glycerol and LiBF4. From this analysis it was stated that the effect of glycerol as a plasticizer on the ionic conductivity results is much more important than the effect obtained by varying the lithium salt content or the effect of the interaction of both variables. Also all the samples were characterized by X-ray diffraction measurements, UV-vis-NIR spectroscopy and scanning electron microscopy (SEM) and impedance spectroscopy. The ionic conductivity results of all analyzed samples as a function of temperature obey predominantly an Arrhenius relationship and the samples are stable up to 160 deg. C. Good conductivity results combined with transparency and good adhesion to the electrodes have shown that gelatin-based GPEs are very promising materials to be used as solid electrolytes in electrochromic devices.

  5. High-Efficiency Glass and Printable Flexible Dye-Sensitized Solar Cells with Water-Based Electrolytes

    Directory of Open Access Journals (Sweden)

    Omar Moudam

    2014-01-01

    Full Text Available The performance of a flexible and glass dye-sensitized solar cell (DSSC with water-based electrolyte solutions is described. High concentrations of alkylamidazoliums were used to overcome the deleterious effect of water and, based on this variable, pure water-based electrolyte DSSCs were tested displaying the highest recorded efficiency so far of 3.45% and 6% for flexible and glass cells, respectively, under a simulated air mass 1.5 solar spectrum illumination at 100 mWcm−2. An improvement in the Jsc with high water content and the positive impact of GuSCN on the enhancement of the performance of pure water-based electrolytes were also observed.

  6. Multianalyte biosensor based on pH-sensitive ZnO electrolyte-insulator-semiconductor structures

    Science.gov (United States)

    Haur Kao, Chyuan; Chen, Hsiang; Ling Lee, Ming; Chun Liu, Che; Ueng, Herng-Yih; Cheng Chu, Yu; Jie Chen, Yu; Ming Chang, Kow

    2014-05-01

    Multianalyte electrolyte-insulator-semiconductor (EIS) sensors with a ZnO sensing membrane annealed on silicon substrate for use in pH sensing were fabricated. Material analyses were conducted using X-ray diffraction and atomic force microscopy to identify optimal treatment conditions. Sensing performance for various ions of Na+, K+, urea, and glucose was also tested. Results indicate that an EIS sensor with a ZnO membrane annealed at 600 °C exhibited good performance with high sensitivity and a low drift rate compared with all other reported ZnO-based pH sensors. Furthermore, based on well-established pH sensing properties, pH-ion-sensitive field-effect transistor sensors have also been developed for use in detecting urea and glucose ions. ZnO-based EIS sensors show promise for future industrial biosensing applications.

  7. Effect of Hydrogen Reduction of Silver Ions on the Performance and Structure of New Solid Polymer Electrolyte PEI/Pebax2533/AgBF4 Composite Membranes

    Institute of Scientific and Technical Information of China (English)

    WANG Yanbei; REN Jizhong; LI Hui; DENG Maicun

    2013-01-01

    In this paper,the effect of hydrogen reduction of silver ions on the performance and structure of new solid polymer electrolyte polyetherimide (PEI)/Pebax2533 (Polynylon12/tetramethylene oxide block copolymer,PA12-PTMO)/AgBF4 composite membranes is investigated.For PEI/Pebax2533/AgBF4 composite membranes prepared with different AgBF4 concentration,the permeances of propylene and ethylene increase with the increase of AgBF4 concentration due to the carrier-facilitated transport,resulting in a high selectivity.But for propylene/propane mixture,the mixed-gas selectivity is lower than its ideal selectivity.The hydrogen reduction strongly influences the membrane performance,which causes the decrease of propylene permeance and the increase of propane permeance.With the increase of hydrogen reduction time,the membranes show a clearly color change from white to brow0n,yielding a great selectivity loss.The data of X-ray diffraction and FT-IR prove that silver ions are reduced to Ag after hydrogen reduction,and aggregated on the surface of PEI/Pebax2533/AgBF4 composite membranes.

  8. Compatibility of lithium difluoro(sulfato)borate-based electrolyte for LiMn2O4 cathode

    Science.gov (United States)

    Li, Shiyou; Liu, Jinliang; Li, Lingxia; Li, Xiaopeng; Jing, Jie; Cui, Xiaoling

    2015-03-01

    Lithium difluoro(sulfato)borate (LiBF2SO4) is investigated as a lithium salt for non-aqueous electrolytes for LiMn2O4 cathode in lithium-ion batteries. Inductively coupled plasma-atomic emission spectrometry analysis is used to analyze the Mn dissolution. Scanning electron microscopy and AC impedance measurements analysis are used to analyze the formation of the surface film on the surface of LiMn2O4 cathode. These results demonstrate that LiBF2SO4-based electrolyte favourably facilitates the formation of an effective and conductive interface film on the cathode surface to improve the stabilization of cathode/electrolyte interface. Besides, LiMn2O4 cells using LiBF2SO4-based electrolyte exerts several advantages, such as stable cycling performance, low cell impedance, low polarization resistance, and good rate performance. It suggests that LiBF2SO4-based electrolyte has good compatibility with LiMn2O4 cathode, and LiBF2SO4 would be a very promising lithium salt for LiMn2O4 cathode in lithium-ion batteries.

  9. Electrochemical oxidation of organic carbonate based electrolyte solutions at lithium metal oxide electrodes

    Energy Technology Data Exchange (ETDEWEB)

    Imhof, R.; Novak, P. [Paul Scherrer Inst. (PSI), Villigen (Switzerland)

    1999-08-01

    The oxidative decomposition of carbonate based electrolyte solutions at practical lithium metal oxide composite electrodes was studied by differential electrochemical mass spectrometry. For propylene carbonate (PC), CO{sub 2} evolution was detected at LiNiO{sub 2}, LiCoO{sub 2}, and LiMn{sub 2}O{sub 4} composite electrodes. The starting point of gas evolution was 4.2 V vs. Li/Li{sup +} at LiNiO{sub 2}, whereas at LiCoO{sub 2} and LiMn{sub 2}O{sub 4}, CO{sub 2} evolution was only observed above 4.8 V vs. Li/Li{sup +}. In addition, various other volatile electrolyte decomposition products of PC were detected when using LiCoO{sub 2}, LiMn{sub 2}O4, and carbon black electrodes. In ethylene carbonate / dimethyl carbonate, CO{sub 2} evolution was only detected at LiNiO{sub 2} electrodes, again starting at about 4.2 V vs. Li/Li{sup +}. (author) 3 figs., 2 refs.

  10. Effect of Eutectic Concentration on Conductivity in PEO:LiX Based Solid Polymer Electrolytes

    Science.gov (United States)

    Zhan, Pengfei; Ganapatibhotla, Lalitha; Maranas, Janna

    Polyethylene oxide (PEO) and lithium salt based solid polymer electrolytes (SPEs) have been widely proposed as a substitution for the liquid electrolyte in Li-ion batteries. As salt concentration varies, these systems demonstrate rich phase behavior. Conductivity as a function of salt concentration has been measured for decades and various concentration dependences have been observed. A PEO:LiX mixture can have one or two conductivity maximums, while some mixtures with salt of high ionic strength will have higher conductivity as the salt concentration decrease. The factors that affect the conductivity are specific for each sample. The universal factor that affects conductivity is still not clear. In this work, we measured the conductivity of a series of PEO:LiX mixtures and statistical analysis shows conductivity is affected by the concentration difference from the eutectic concentration (Δc). The correlation with Δc is stronger than the correlation with glass transition temperature. We believe that at the eutectic concentration, during the solidification process, unique structures can form which aid conduction. Currently at Dow Chemical.

  11. Conductivity enhancement via chemical modification of chitosan based green polymer electrolyte

    International Nuclear Information System (INIS)

    The potential of carboxymethyl chitosan as a green polymer electrolyte has been explored. Chitosan produced from partial deacetylation of chitin was reacted with monochloroacetic acid to form carboxymethyl chitosan. A green polymer electrolyte based chitosan and carboxymethyl chitosan was prepared by solution-casting technique. The powder and films were characterized by reflection Fourier transform infrared (ATR-FTIR) spectroscopy, 1H nuclear magnetic resonance, elemental analysis and X-ray diffraction, electrochemical impedance spectroscopy, and scanning electron microscopy. The shift of wavenumber that represents hydroxyl and amine stretching confirmed the polymer solvent complex formation. The XRD spectra results show that chemical modification of chitosan has improved amorphous properties of chitosan. The ionic conductivity was found to increase by two magnitudes higher with the chemical modification of chitosan. The highest conductivity achieved was 3.6 × 10−6 S cm−1 for carboxymethyl chitosan at room temperature and 3.7 × 10−4 S cm−1 at 60 °C

  12. Comprehensive Insights into the Reactivity of Electrolytes Based on Sodium Ions.

    Science.gov (United States)

    Eshetu, Gebrekidan Gebresilassie; Grugeon, Sylvie; Kim, Huikyong; Jeong, Sangsik; Wu, Liming; Gachot, Gregory; Laruelle, Stephane; Armand, Michel; Passerini, Stefano

    2016-03-01

    We report a systematic investigation of Na-based electrolytes that comprise various NaX [X=hexafluorophosphate (PF6 ), perchlorate (ClO4 ), bis(trifluoromethanesulfonyl)imide (TFSI), fluorosulfonyl-(trifluoromethanesulfonyl)imide (FTFSI), and bis(fluorosulfonyl)imide (FSI)] salts and solvent mixtures [ethylene carbonate (EC)/dimethyl carbonate (DMC), EC/diethyl carbonate (DEC), and EC/propylene carbonate (PC)] with respect to the Al current collector stability, formation of soluble degradation compounds, reactivity towards sodiated hard carbon (Nax -HC), and solid-electrolyte interphase (SEI) layer formation. Cyclic voltammetry demonstrates that the stability of Al is highly influenced by the nature of the anions, solvents, and additives. GC-MS analysis reveals that the formation of SEI telltales depends on the nature of the linear alkyl carbonates and the battery chemistry (Li(+) vs. Na(+) ). FTIR spectroscopy shows that double alkyl carbonates are the main components of the SEI layer on Nax -HC. In the presence of Na salts, EC/DMC and EC/DEC presented a higher reactivity towards Nax -HC than EC/PC. For a fixed solvent mixture, the onset temperature follows the sequence NaClO4

  13. Copper-ion conducting solid-polymer electrolytes based on polyacrylonitrile (PAN)

    Energy Technology Data Exchange (ETDEWEB)

    Perera, Kumudu; Dissanayake, M.A.K.L.; Bandaranayake, P.W.S.K. [University of Peradeniya (Slovakia). Dept. of Physics

    2000-07-01

    Two copper-ion conducting solid-polymer electrolyte systems based on polyacrylonitrile (PAN) have been synthesized and characterized using DC polarization tests and impedance measurements. The system with 21 mol% PAN: 30 mol% EC: 45 mol% PC: 04 mol% CuCNS has a room temperature conductivity of 3.30 x 10{sup -5} S cm{sup -1} and an activation energy of 0.25 eV. The conductivity versus temperature plot obeys an Arrhenius type variation. It is predominantly an ionic conductor with negligible electronic conductivity. It has a high anionic transference number (t = 0.80) due to CNS{sup -} ions and a low cationic transference number (t{sub +} = 0.20) due to Cu{sup +} ions. The system with 20 mol% PAN: 41 mol% EC: 34 mol% PC: 5 mol% CuTf has a room temperature conductivity of 4.10 x l0{sup -3} S cm{sup -1} and an activation energy of 0.14 eV. It obeys the VTF equation. The system appears to be a mixed conductor with a cationic (Cu{sup 2+}/ Cu{sup +}) transference number of t{sub +} = 0.50 and an electronic transference number of t{sub e} = 0.50 with negligible anionic conductivity. Both systems yielded free standing stable polymer electrolyte films (Author)

  14. Physical and electrochemical characteristics of supercapacitors based on carbide derived carbon electrodes in aqueous electrolytes

    Science.gov (United States)

    Eskusson, Jaanus; Jänes, Alar; Kikas, Arvo; Matisen, Leonard; Lust, Enn

    FIB-SEM, XPS and gas adsorption methods have been used for the characterisation of physical properties of microporous carbide derived carbon electrodes prepared from Mo 2C at 600 °C (noted as CDC-Mo 2C). Cyclic voltammetry, constant current charge/discharge, and electrochemical impedance spectroscopy have been applied to establish the electrochemical characteristics for supercapacitors consisting of the 1 M Na 2SO 4, KOH, tetraethyl ammonium iodide or 6 M KOH aqueous electrolyte and CDC-Mo 2C electrodes. The N 2 sorption values obtained have been correlated with electrochemical characteristics for supercapacitors in various aqueous electrolytes. The maximum gravimetric energy, E max, and gravimetric power, P max, for supercapacitors (taking into consideration the active material weight) have been obtained at cell voltage 0.9 V for 6 M KOH aqueous supercapacitor (E max = 5.7 Wh kg -1 and P max = 43 kW kg -1). For 1 M TEAI based SC somewhat higher E max (6.2 Wh kg -1) and comparatively low P max (7.0 kW kg -1) have been calculated.

  15. Enhanced Performance of a Lithium-Sulfur Battery Using a Carbonate-Based Electrolyte.

    Science.gov (United States)

    Xu, Zhixin; Wang, Jiulin; Yang, Jun; Miao, Xiaowei; Chen, Renjie; Qian, Ji; Miao, Rongrong

    2016-08-22

    The lithium-sulfur battery is regarded as one of the most promising candidates for lithium-metal batteries with high energy density. However, dendrite Li formation and low cycle efficiency of the Li anode as well as unstable sulfur based cathode still hinder its practical application. Herein a novel electrolyte (1 m LiODFB/EC-DMC-FEC) is designed not only to address the above problems of Li anode but also to match sulfur cathode perfectly, leading to extraordinary electrochemical performances. Using this electrolyte, lithium|lithium cells can cycle stably for above 2000 hours and the average Coulumbic efficiency reaches 98.8 %. Moreover, the Li-S battery delivers a reversible capacity of about 1400 mAh g(-1) sulfur with retention of 89 % for 1100 cycles at 1 C, and a capacity above 1100 mAh g(-1) sulfur at 10 C. The more advantages of this cell system are its outstanding cycle stability at 60 °C and no self-discharge phenomena. PMID:27461554

  16. Ionic liquids based on S-alkylthiolanium cations and TFSI anion as potential electrolytes

    Institute of Scientific and Technical Information of China (English)

    ZHANG HuanQi; YANG Li; FANG ShaoHua; PENG ChengXin; LUO HongJun

    2009-01-01

    New ionic liquids based on S-alkylthiolanium cations with TFSI anions were synthesized and charac-terized.The physical and electrochemical properties,including melting point,thermal stability,solubil-ity,viscosity,conductivity and electrochemical window,were reported.Relation between these proper-ties and the structure of the cations was discussed.In this series,T4TFSI and T5TFSI have melting points below -60℃,and their conductivities are 2.10 mS/cm and 1.46 mS/cm;their electrochemical windows are 4.1 V and 4.5 V at room temperature.These cyclic alkylthiolanium-based ionic liquids are promising as novel electrolytes in various electrochemical devices,especially under low temperature condition.

  17. Receiver based PAPR reduction in OFDMA

    KAUST Repository

    Ali, Anum Z.

    2014-05-01

    High peak-to-average power ratio is one of the major drawbacks of orthogonal frequency division multiplexing (OFDM). Clipping is the simplest peak reduction scheme, however, it requires clipping mitigation at the receiver. Recently compressed sensing has been used for clipping mitigation (by exploiting the sparse nature of clipping signal). However, clipping estimation in multi-user scenario (i.e., OFDMA) is not straightforward as clipping distortions overlap in frequency domain and one cannot distinguish between distortions from different users. In this work, a collaborative clipping removal strategy is proposed based on joint estimation of the clipping distortions from all users. Further, an effective data aided channel estimation strategy for clipped OFDM is also outlined. Simulation results are presented to justify the effectiveness of the proposed schemes. © 2014 IEEE.

  18. Novel choline-based ionic liquids as safe electrolytes for high-voltage lithium-ion batteries

    Science.gov (United States)

    Yong, Tianqiao; Zhang, Lingzhi; Wang, Jinglun; Mai, Yongjin; Yan, Xiaodan; Zhao, Xinyue

    2016-10-01

    Three choline-based ionic liquids functionalized with trimethylsilyl, allyl, and cynoethyl groups are synthesized in an inexpensive route as safe electrolytes for high-voltage lithium-ion batteries. The thermal stabilities, viscosities, conductivities, and electrochemical windows of these ILs are reported. Hybrid electrolytes were formulated by doping with 0.6 M LiPF6/0.4 M lithium oxalydifluoroborate (LiODFB) as salts and dimethyl carbonate (DMC) as co-solvent. By using 0.6 M LiPF6/0.4 M LiODFB trimethylsilylated choline-based IL (SN1IL-TFSI)/DMC as electrolyte, LiCoO2/graphite full cell showed excellent cycling performance with a capacity of 152 mAh g-1 and 99% capacity retention over 90 cycles at a cut-off voltage of 4.4 V. The propagation rate of SN1IL-TFSI)/DMC electrolyte is only one quarter of the commercial electrolyte (1 M LiPF6 EC/DEC/DMC, v/v/v = 1/1/1), suggesting a better safety feature.

  19. Electrolytes with Improved Safety Developed for High Specific Energy Li-Ion Cells with Si-Based Anodes

    Science.gov (United States)

    Smart, M. C.; Krause, F. C.; Hwang, C.; Soler, J.; West, W. C.; Ratnakumar, B. V.; Prakash, G. K. S.

    2012-01-01

    A number of electrolyte formulations that have improved safety characteristics have been developed for use with high capacity silicon-based anodes. To improve the compatibility with Si-based anodes, a number of technical approaches have been employed, including: (1) the use of mono-fluoroethylene carbonate (FEC) in conjunction with, or in lieu of, ethylene carbonate (EC), (2) the use of high proportions of fluorinated co-solvents, (3) the use of vinylene carbonate (VC) to stabilize the Si/C electrode, and (4) the use of lithium bis(oxalato)borate (LiBOB) to improve the compatibility of the electrolyte when Si/C electrodes are used in conjunction with high voltage cathodes. Candidate electrolytes were studied in Li/Si-C and Si-C/ Li(MnNiCo)O2 (NMC) coin cells, as well as in larger Si-C/NMC three-electrode cells equipped with lithium reference electrodes. In summary, many electrolytes that contain triphenyl phosphate (TPP), which is used as a flame retardant additive up to concentrations of 15 volume percent, and possess FEC as a co-solvent have been demonstrated to outperform the all-carbonate baseline electrolytes when evaluated in Si-C/ Li(MnNiCo)O2 cells.

  20. Thermal reactions of mesocarbon microbead (MCMB) particles in LiPF 6-based electrolyte

    Science.gov (United States)

    Xiao, Ang; Li, Wentao; Lucht, Brett L.

    The thermal reaction of ternary electrolyte (1.0 M LiPF 6 in 1:1:1 ethylene carbonate/dimethyl carbonate/diethyl carbonate) with mesocarbon microbeads (MCMB) particles was investigated by the combined use of NMR, GC-MS, FTIR-ATR, TGA, XPS and SEM/EDS-element map. The thermal decomposition of ternary electrolyte is not inhibited by the presence of MCMB particles. The chemical composition and morphology of the surface of MCMB particles changes significantly upon storage in the presence of ternary electrolyte. Electrolyte decomposition products including oligocarbonates, oligoethylene oxides, polyethylene oxide (PEO), lithium fluorophosphates (Li xPO yF z), and lithium fluoride are deposited on the surface of MCMB particles. The concentration of decomposition products on the surface of MCMB increases with increased storage time and temperature. The addition of dimethyl acetamide (DMAc) impedes the thermal decomposition of the electrolyte and deposition of electrolyte decomposition products on the surface of MCMB.

  1. Thin hybrid electrolyte based on garnet-type lithium-ion conductor Li7La3Zr2O12 for 12 V-class bipolar batteries

    Science.gov (United States)

    Yoshima, Kazuomi; Harada, Yasuhiro; Takami, Norio

    2016-01-01

    Thin hybrid electrolytes based on lithium-ion conducting ceramics with a few micrometers thickness have been studied in order to be practically applied to 12 V-class bipolar battery with liquid-free and separator-free. A cubic garnet-type Li7La3Zr2O12 (LLZ)-based hybrid electrolyte composed of LLZ particles coated with 4 wt% polyacrylonitrile (PAN)-based gel polymer electrolyte was prepared as the thin electrolyte layer, which reduced the internal resistance of LiMn0.8Fe0.2PO4(LMFP)/Li4Ti5O12(LTO) cells and enabled discharge at low temperatures. The conductivity of the LLZ-based hybrid electrolyte at 25°C was one order of magnitude higher than that of the LLZ solid electrolyte and comparable to that of the PAN-based gel polymer. The activation energy for ionic conductivity of the hybrid electrolyte was significantly smaller than that of the gel polymer electrolyte. The fabricated 12 V-class bipolar LMFP/LTO battery using the thin LLZ-based hybrid electrolyte layer exhibited good performance in terms of discharge rate capability, operating in the wide temperature range of -40°C to 80°C, and charge-discharge cycling comparable to those of conventional lithium-ion batteries.

  2. Compatibility of lithium difluoro(sulfato)borate-based electrolyte for LiMn{sub 2}O{sub 4} cathode

    Energy Technology Data Exchange (ETDEWEB)

    Li, Shiyou; Liu, Jinliang; Li, Lingxia; Li, Xiaopeng; Jing, Jie; Cui, Xiaoling, E-mail: xlcuilw@163.com

    2015-03-01

    Highlights: • LiBF{sub 2}SO{sub 4} was investigated as a novel salt for advanced lithium-ion batteries. • LiBF{sub 2}SO{sub 4}-EC/DEC shows excellent film-forming characteristic on the surface of LiMn{sub 2}O{sub 4}. • LiBF{sub 2}SO{sub 4}-based electrolyte has good compatibility with LiMn{sub 2}O{sub 4} cathode. - Abstract: Lithium difluoro(sulfato)borate (LiBF{sub 2}SO{sub 4}) is investigated as a lithium salt for non-aqueous electrolytes for LiMn{sub 2}O{sub 4} cathode in lithium-ion batteries. Inductively coupled plasma-atomic emission spectrometry analysis is used to analyze the Mn dissolution. Scanning electron microscopy and AC impedance measurements analysis are used to analyze the formation of the surface film on the surface of LiMn{sub 2}O{sub 4} cathode. These results demonstrate that LiBF{sub 2}SO{sub 4}-based electrolyte favourably facilitates the formation of an effective and conductive interface film on the cathode surface to improve the stabilization of cathode/electrolyte interface. Besides, LiMn{sub 2}O{sub 4} cells using LiBF{sub 2}SO{sub 4}-based electrolyte exerts several advantages, such as stable cycling performance, low cell impedance, low polarization resistance, and good rate performance. It suggests that LiBF{sub 2}SO{sub 4}-based electrolyte has good compatibility with LiMn{sub 2}O{sub 4} cathode, and LiBF{sub 2}SO{sub 4} would be a very promising lithium salt for LiMn{sub 2}O{sub 4} cathode in lithium-ion batteries.

  3. Physics Based Electrolytic Capacitor Degradation Models for Prognostic Studies under Thermal Overstress

    Science.gov (United States)

    Kulkarni, Chetan S.; Celaya, Jose R.; Goebel, Kai; Biswas, Gautam

    2012-01-01

    Electrolytic capacitors are used in several applications ranging from power supplies on safety critical avionics equipment to power drivers for electro-mechanical actuators. This makes them good candidates for prognostics and health management research. Prognostics provides a way to assess remaining useful life of components or systems based on their current state of health and their anticipated future use and operational conditions. Past experiences show that capacitors tend to degrade and fail faster under high electrical and thermal stress conditions that they are often subjected to during operations. In this work, we study the effects of accelerated aging due to thermal stress on different sets of capacitors under different conditions. Our focus is on deriving first principles degradation models for thermal stress conditions. Data collected from simultaneous experiments are used to validate the desired models. Our overall goal is to derive accurate models of capacitor degradation, and use them to predict performance changes in DC-DC converters.

  4. Green polymer electrolytes based on chitosan and 1-butyl-3-methylimidazolium acetate

    Energy Technology Data Exchange (ETDEWEB)

    Shamsudin, Intan Juliana [Chemistry Department, Centre for Defence Foundation Studies, National Defence University of Malaysia, 57000 Kuala Lumpur (Malaysia); Ahmad, Azizan; Hassan, Nur Hasyareeda [School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor Darul Ehsan (Malaysia)

    2014-09-03

    Green polymer electrolytes based on chitosan as the polymer matrix and ionic liquid 1-butyl-3-methylimidazolium acetate [Bmim][OAc] as charge carriers were prepared by solution casting technique. Complexes with various amount of ionic liquid loading were investigated as possible ionic conducting polymers. The ionic conductivity was found to increase with increasing weight percent of ionic liquid. The highest ionic conductivity of the charged chitosan-[Bmim][OAc] was 2.44 × 10{sup −3} S cm{sup −1} at 90 wt.% of [Bmim][OAc] content at ambient temperature. Attenuated Total Reflection Fourier Transform infrared (ATR-FTIR) spectroscopy has proven the interaction between chitosan and [Bmim][OAc]. X-ray Diffraction (XRD) has shown that the amorphosity of the complexes increase as the amount of [Bmim][OAc] increase.

  5. Magnetic resonance and conductivity study of a gelatin-based polymer gel electrolyte

    International Nuclear Information System (INIS)

    This work reports results from proton nuclear magnetic resonance (NMR), electron paramagnetic resonance (EPR) and complex impedance spectroscopy of gelatin-based polymer gel electrolytes containing chloridric acid, cross-linked with formaldehyde and plasticized with glycerol. Ionic conductivity of 4 × 10−5 S/cm were obtained at room temperature for samples prepared with 0.1 M of HCl. Proton (1H) lineshapes and spin-lattice relaxation times were measured as a function of temperature. Activation energies extracted from the 1H NMR relaxation data are in the range of 23–25 kJ/mol. The EPR spectra, which were carried out in samples doped with copper perchlorate, were interpreted with the aid of an axial spin Hamiltonian and indicate the presence of two different Cu2+ species in axially distorted sites. Copper complexation with both hydrogen and nitrogen was verified by electron spin-echo envelope modulation (ESEEM) techniques.

  6. An Electrically Driven and Readable Molecular Monolayer Switch Based on a Solid Electrolyte.

    Science.gov (United States)

    Marchante, Elena; Crivillers, Núria; Buhl, Moritz; Veciana, Jaume; Mas-Torrent, Marta

    2016-01-01

    The potential application of molecular switches as active elements in information storage has been demonstrated through numerous works. Importantly, such switching capabilities have also been reported for self-assembled monolayers (SAMs). SAMs of electroactive molecules have recently been exploited as electrochemical switches. Typically, the state of these switches could be read out through their optical and/or magnetic response. These output reading processes are difficult to integrate into devices, and furthermore, there is a need to use liquid environments for switching the redox-active molecular systems. In this work, both of these challenges were overcome by using an ionic gel as the electrolyte medium, which led to an unprecedented solid-state device based on a single molecular layer. Moreover, electrochemical impedance has been successfully exploited as the output of the system.

  7. Effects of Silica Nanostructures in Poly(ethylene oxide)-Based Composite Polymer Electrolytes.

    Science.gov (United States)

    Mohanta, Jagdeep; Anwar, Shahid; Si, Satyabrata

    2016-06-01

    The present work describes the synthesis of some poly(ethylene oxide)-based nanocomposite polymer electrolyte films using various silica nanostructures as the inorganic filler by simple solution mixing technique, in which the nature of the silica nanostructures play a vital role in modulating their electrochemical performances at room temperature. The silica nanostructures are prepared by ammonical hydrolysis of tetraethyl orthosilicate following the modified St6ber method. The resulting films are characterized by X-ray diffraction and differential scanning calorimeter to study their crystallinity. Room temperature AC impedance spectroscopy is utilized to determine the Li+ ion conductivity of the resulting films. The observed conductivity values of various NCPE films depend on the nature of silica filling as well as on their surface characteristics and also on the varying PEO-Li+ ratio, which is observed to be in the order of 10(-7)-10(-6) S cm(-1). PMID:27427686

  8. High-efficiency dye-sensitized solar cells using ferrocene-based electrolytes and natural photosensitizers

    Science.gov (United States)

    Sönmezoğlu, Savaş; Akyürek, Cafer; Akin, Seçkin

    2012-10-01

    A new and promising dye-sensitized solar cell (DSSC) bilayer design was developed using an Fe2+/Fe3+ (ferrocene) liquid electrolyte and natural dyes extracted from Hypericum perforatum, Rubia tinctorum L. and Reseda luteola. The photovoltaic parameters controlling the device performance were then investigated. A DSSC based on quercetin dye displayed the most efficient solar to electricity conversion efficiency compared with other dyes with a maximum η value of 2.17%. Maximum overall conversion efficiencies under simulated sunlight that was comparable to natural photosynthesis were increased by 15%. The identification of appropriate additives for improving VOC without causing dye degradation may result in further enhancement of cell performance, making the practical application of such systems more suitable for achieving economically viable solar energy devices.

  9. Hybrid capacitors utilizing halogen-based redox reactions at interface between carbon positive electrode and aqueous electrolytes

    Science.gov (United States)

    Yamazaki, Shigeaki; Ito, Tatsuya; Murakumo, Yuka; Naitou, Masashi; Shimooka, Toshiharu; Yamagata, Masaki; Ishikawa, Masashi

    2016-09-01

    We propose novel hybrid capacitors (HCs) with electrolyte-involved redox reactions of bromide or iodide species by pretreatment of an activated carbon positive electrode. The treatment is simple; impregnation of pores at an activated carbon fiber cloth (ACFC) as a positive electrode with bromine- or iodine-containing water before cell assembly. The treated positive electrode is applied to a HC cell with a non-treated negative electrode of ACFC and its electrochemical performance is investigated by galvanostatic cycling and leakage current tests. Few studies on such "electrolytic" charge storage systems have provided acceptable capacitor performance because of inevitable self-discharge caused by diffusion of charged species form an electrode to the other one through an electrolyte. Nevertheless, our electrolyte-redox-based HCs show excellent performance without undesirable diffusion of charged species. Moreover, the present HC utilizing a bromide redox system fulfills a practical cell voltage of 1.8 V in spite of an aqueous electrolyte system. This high voltage provides excellent energy density, which is 5 times higher than that in a conventional aqueous electric double-layer capacitor (EDLC), and 1.2 times higher even than that in a 2.7 V-class non-aqueous EDLC, while keeping high charge-discharge rate capability.

  10. Thermostable gel polymer electrolyte based on succinonitrile and ionic liquid for high-performance solid-state supercapacitors

    Science.gov (United States)

    Pandey, Gaind P.; Liu, Tao; Hancock, Cody; Li, Yonghui; Sun, Xiuzhi Susan; Li, Jun

    2016-10-01

    A flexible, free-standing, thermostable gel polymer electrolyte based on plastic crystalline succinonitrile (SN) and ionic liquid 1-butyl-3-methylimidazolium tetrafluoroborate (BMImBF4) entrapped in copolymer poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) is prepared and optimized for application in solvent-free solid-state supercapacitors. The synthesized gel polymer electrolyte exhibits a high ionic conductivity over a wide temperature range (from ∼5 × 10-4 S cm-1 at -30 °C up to ∼1.5 × 10-2 S cm-1 at 80 °C) with good electrochemical stability window (-2.9 to 2.5 V). Thermal studies confirm that the SN containing gel polymer electrolyte remains stable in the same gel phase over a wide temperature range from -30 to 90 °C. The electric double layer capacitors (EDLCs) have been fabricated using activated carbon as active materials and new gel polymer electrolytes. Electrochemical performance of the EDLCs is assessed through cyclic voltammetry, galvanostatic charge-discharge cycling and impedance spectroscopy. The EDLC cells with the proper SN-containing gel polymer electrolyte has been found to give high specific capacitance 176 F g-1 at 0.18 A g-1 and 138 F g-1 at 8 A g-1. These solid-state EDLC cells show good cycling stability and the capability to retain ∼80% of the initial capacitance after 10,000 cycles.

  11. Enhanced cycling performance of a Li metal anode in a dimethylsulfoxide-based electrolyte using highly concentrated lithium salt for a lithium-oxygen battery

    Science.gov (United States)

    Togasaki, Norihiro; Momma, Toshiyuki; Osaka, Tetsuya

    2016-03-01

    Stable charge-discharge cycling behavior for a lithium metal anode in a dimethylsulfoxide (DMSO)-based electrolyte is strongly desired of lithium-oxygen batteries, because the Li anode is rapidly exhausted as a result of side reactions during cycling in the DMSO solution. Herein, we report a novel electrolyte design for enhancing the cycling performance of Li anodes by using a highly concentrated DMSO-based electrolyte with a specific Li salt. Lithium nitrate (LiNO3), which forms an inorganic compound (Li2O) instead of a soluble product (Li2S) on a lithium surface, exhibits a >20% higher coulombic efficiency than lithium bis(trifluoromethanesulfonyl)imide, lithium bis(fluorosulfonyl)imide, and lithium perchlorate, regardless of the loading current density. Moreover, the stable cycling of Li anodes in DMSO-based electrolytes depends critically on the salt concentration. The highly concentrated electrolyte 4.0 M LiNO3/DMSO displays enhanced and stable cycling performance comparable to that of carbonate-based electrolytes, which had not previously been achieved. We suppose this enhancement is due to the absence of free DMSO solvent in the electrolyte and the promotion of the desolvation of Li ions on the solid electrolyte interphase surface, both being consequences of the unique structure of the electrolyte.

  12. Organic dopant added polyvinylidene fluoride based solid polymer electrolytes for dye-sensitized solar cells

    Science.gov (United States)

    Senthil, R. A.; Theerthagiri, J.; Madhavan, J.

    2016-02-01

    The effect of phenothiazine (PTZ) as dopant on PVDF/KI/I2 electrolyte was studied for the fabrication of efficient dye-sensitized solar cell (DSSC). The different weight percentage (wt%) ratios (0, 20, 30, 40 and 50%) of PTZ doped PVDF/KI/I2 electrolyte films were prepared by solution casting method using DMF as a solvent. The following techniques such as Fourier transform infrared (FT-IR), differential scanning calorimetry (DSC), X-ray diffractometer (XRD) and AC-impedance analysis have been employed to characterize the prepared polymer electrolyte films. The FT-IR studies revealed the complex formation between PVDF/KI/I2 and PTZ. The crystalline and amorphous nature of polymer electrolytes were confirmed by DSC and XRD analysis respectively. The ionic conductivities of polymer electrolyte films were calculated from the AC-impedance analysis. The undoped PVDF/KI/I2 electrolyte exhibited the ionic conductivity of 4.68×10-6 S cm-1 and this value was increased to 7.43×10-5 S cm-1 when PTZ was added to PVDF/KI/I2 electrolyte. On comparison with different wt% ratios, the maximum ionic conductivity was observed for 20% PTZ-PVDF/KI/I2 electrolyte. A DSSC assembled with the optimized wt % of PTZ doped PVDF/KI/I2 electrolyte exhibited a power conversion efficiency of 2.92%, than the undoped PVDF/KI/I2 electrolyte (1.41%) at similar conditions. Hence, the 20% PTZ-PVDF/KI/I2 electrolyte was found to be optimal for DSSC applications.

  13. Polymer electrolyte based on crosslinked poly(glycidyl methacrylate) and 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide

    Energy Technology Data Exchange (ETDEWEB)

    Fei, Beatrice Wong Chui; Hanifah, Sharina Abu; Ahmad, Azizan; Hassan, Nur Hasyareeda [School of Chemical Sciences and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43000 Bangi, Selangor Darul Ehsan (Malaysia)

    2015-09-25

    Polymer electrolytes based on crosslinked poly(glycidyl methacrylate) as polymer host and 1-butyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (BmimTFSI) as incorporated salt were prepared by in-situ photopolymerization technique. The complexes with different mass ratio of glycidyl methacrylate (GMA) monomer to BmimTFSI were investigated. The ionic conductivity of the polymer electrolyte was increased and reach the highest value of 7.50 × 10{sup −4} S cm{sup −1} at the ratio of 3:7 (GMA: BmimTFSI). The interaction between the polymer host and ionic liquid was proved by Attenuated Total Reflectance-Fourier Transformation Infra-Red Spectroscopy (ATR-FTIR). Meanwhile, the X-ray diffraction analysis shows the amorphousity of the polymer electrolyte film increase with the ionic liquid ratio.

  14. Physico- and electrochemistry of composite electrolytes based on PEODME-LiTFSI with TiO 2

    Science.gov (United States)

    Moskwiak, M.; Giska, I.; Borkowska, R.; Zalewska, A.; Marczewski, M.; Marczewska, H.; Wieczorek, W.

    The effect of fumed TiO 2 fillers (pure and modified by H 2SO 4) on ionic conductivity of composite electrolytes based on poly(ethylene oxide) dimethyl ether (PEODME) oligomer (M w = 500) doped with lithium bis-(trifluoromethanesulfonyl)imide LiN(CF 3SO 2) 2 (LiTFSI) are studied by differential scanning calorimetry (DSC), Fourier transform infrared spectroscopy (FT-IR) and complex impedance methods. The electrochemical stability of the electrolytes in the potential range of 4 V versus Li electrode has been confirmed by voltammetric measurements. Li electrode reactions have been followed by means of impedance spectroscopy. The growth in time of the resistance of the interfacial (Li electrode-polymer electrolyte) layers was inhibited upon the addition of fillers.

  15. PbO2 based composite materials deposited from suspension electrolytes: electrosynthesis, physico-chemical and electrochemical properties

    OpenAIRE

    Velichenko, Alexander; Knysh, Valentina; Luk’yanenko, Tatiana; Dmitrikova, Larisa; Velichenko, Yulia; Devilliers, Didier

    2012-01-01

    Composite materials based on PbO2 containing TiO2 or ZrO2 were prepared from electrolytes containing a suspension of TiO2 or ZrO2. The contents of foreign oxides in the composite depend on the electrolyte composition and conditions of deposition. When a dispersed phase is incorporated into the composite coating, the dimensions of lead dioxide crystals decrease to submicro- and nano-size. Physico-chemical properties and electrocatalytic activity of composite materials are mainly determin...

  16. UV-cured Al2O3-laden cellulose reinforced polymer electrolyte membranes for Li-based batteries

    International Nuclear Information System (INIS)

    A methacrylate based plasticised polymer electrolyte membrane is prepared via a rapid and facile UV curing process, the major concerns of mechanical integrity are overcome by simply using appropriately modified cellulose handsheet laden with nano-sized acidic alumina particles as a reinforcement. The use of the cellulose handsheets greatly enhances the flexibility and mechanical properties of the membrane while the addition of alumina particles helps to maintain satisfactory conductivity values. The reinforced composite electrolyte membrane is also tested in a real lithium cell, exhibiting excellent performance which account for its use in futuristic lithium batteries having low cost, environmentally friendly and easily scalable properties

  17. Improved low temperature performance of lithium ion cells with quaternary carbonate-based electrolytes

    Science.gov (United States)

    Smart, M. C.; Ratnakumar, B. V.; Whitcanack, L. D.; Chin, K. B.; Surampudi, S.; Croft, H.; Tice, D.; Staniewicz, R.

    2002-01-01

    In order to enable future missions involving the exploration of the surface of Mars with Landers and Rovers, NASA desires long life, high energy density rechargeable batteries which can operate well at very low temperature (down to 40(deg)C). Lithium-ion technology has been identified as being the most promising chemistry, due to high gravimetric and volumetric energy densities, as well as, long life characteristics. However, the state-of-art (SOA) technology is not sufficient to meet the needs of many applications that require excellent low temperature capabilities. To further improve this technology, work at JF'L has been focused upon developing electrolytes that result in lithium-ion cells with wider temperature ranges of operation. These efforts have led to the identification of a number of ternary and quaternary, all carbonate-based electrolytes that have been demonstrated to result in improved low temperature performance in experimental three-electrode MCMB carbon/LiNio.sCoo.zOz cells. A number of electrochemical characterization techniques were performed on these cells (i.e., Tafel polarization measurements, linear polarization measurements, and electrochemical impedance spectroscopy (EIS)) to further enhance our understanding of the performance limitations at low temperature. The most promising electrolyte formulations, namely 1 .O M LiPF6EC+DEC+DMC+EMC (1 : 1: 1 :2 v/v) and 1 .O M LiPF6 EC+DEC+DMC+EMC (1 : 1 : 1 :3 v/v), were incorporated into SAFT prototype DD-size (9 Ahr) lithium- cells for evaluation. A number of electrical tests were performed on these cells, including rate characterization as a function of temperature, cycle life characterization at different temperatures, as well as, many mission specific characterization test to determine their viability to enable future missions to Mars. Excellent performance was observed with the prototype DD-size cells over a wide temperature range (-50 to 4OoC), with high specific energy being delivered at very

  18. Novel polymer electrolytes based on cationic polyurethane with different alkyl chain length

    Science.gov (United States)

    Liu, Libin; Wu, Xiwen; Li, Tianduo

    2014-03-01

    A series of comb-like cationic polyurethanes (PUs) were synthesized by quaternizing different bromoalkane (C2H5Br, C8H17Br, and C14H29Br) with polyurethane. Solid polymer electrolytes were prepared by complexes cationic PUs with different content of LiClO4. All the solid polymer electrolytes had sufficient thermal stability as confirmed by TGA and exhibited a single-phase behavior evidenced by DSC results. For these electrolytes, FT-IR spectra indicated the formation of polymer-ion complexes. The ac impedance spectra show that the conductivity of the electrolytes follow the Arrhenius behavior, and ionic conductivity is associated with both the charge migration of ions between coordination sites and transmission between aggregates, as confirmed by FT-IR and SEM. Alkyl quaternary ammonium salts in the polymer backbone are recognized as inherent plasticizers, which make the electrolytes exhibit liquid-like behavior. The plasticizing effect of PU-C8 and PU-C14 electrolytes are more effective than that of PU-C2 electrolyte. Maximum ionic conductivity at room temperature for PU-C8 electrolytes containing 50 wt% LiClO4 reached 1.1 × 10-4 S cm-1. This work provides a new research clue that alkyl quaternary ammonium salts could be used as inherent plasticizers and hence make the system behave like a liquid with high ionic conductivity, while preserving the dimensional stability of the solids.

  19. A quasi-direct methanol fuel cell system based on blend polymer membrane electrolytes

    DEFF Research Database (Denmark)

    Li, Qingfeng; Hjuler, Hans Aage; Hasiotis, C.;

    2002-01-01

    On the basis of blend polymer electrolytes of polybenzimidazole and sulfonated polysulfone, a polymer electrolyte membrane fuel cell was developed with an operational temperature up to 200degrees C. Due to the high operational temperature, the fuel cell can tolerate 1.0-3.0 vol % CO in the fuel...

  20. Electrochemical characterization of an ambient temperature rechargeable Li battery based on low molecular weight polymer electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Bonino, F.; Croce, F.; Panero, S. (Dept. of Chemistry, Univ. of Rome ' La Sapienza' , Rome (Italy))

    1994-06-01

    Preliminary applications of low molecular weight polymer electrolyte (PEG) and lithium salt in lithium rechargeable batteries have been reported. The electrochemical characteristics of these electrolytes have been tested by cyclic voltammetry, charge-discharge cycles and ac impedance methods. Surface layers appear to be present on both electrodes, but they develop upon time with different extension

  1. The effect of electrolyte composition on the electroreduction of CO2 to CO on Ag based gas diffusion electrodes.

    Science.gov (United States)

    Verma, Sumit; Lu, Xun; Ma, Sichao; Masel, Richard I; Kenis, Paul J A

    2016-03-14

    The electroreduction of CO2 to C1-C2 chemicals can be a potential strategy for utilizing CO2 as a carbon feedstock. In this work, we investigate the effect of electrolytes on the electroreduction of CO2 to CO on Ag based gas diffusion electrodes. Electrolyte concentration was found to play a major role in the process for the electrolytes (KOH, KCl, and KHCO3) studied here. Several fold improvements in partial current densities of CO (jCO) were observed on moving from 0.5 M to 3.0 M electrolyte solution independent of the nature of the anion. jCO values as high as 440 mA cm(-2) with an energy efficiency (EE) of ≈ 42% and 230 mA cm(-2) with EE ≈ 54% were observed when using 3.0 M KOH. Electrochemical impedance spectroscopy showed that both the charge transfer resistance (Rct) and the cell resistance (Rcell) decreased on moving from a 0.5 M to a 3.0 M KOH electrolyte. Anions were found to play an important role with respect to reducing the onset potential of CO in the order OH(-) (-0.13 V vs. RHE) liquids and 1 : 2 choline Cl urea based deep eutectic solvents (DESs) have been used for CO2 capture but exhibit low conductivity. Here, we investigate if the addition of KCl to such solutions can improve conductivity and hence jCO. Electrolytes containing KCl in combination with EMIM Cl, choline Cl, or DESs showed a two to three fold improvement in jCO in comparison to those without KCl. Using such mixtures can be a strategy for integrating the process of CO2 capture with CO2 conversion. PMID:26661416

  2. Dimension reduction based on weighted variance estimate

    Institute of Scientific and Technical Information of China (English)

    2009-01-01

    In this paper, we propose a new estimate for dimension reduction, called the weighted variance estimate (WVE), which includes Sliced Average Variance Estimate (SAVE) as a special case. Bootstrap method is used to select the best estimate from the WVE and to estimate the structure dimension. And this selected best estimate usually performs better than the existing methods such as Sliced Inverse Regression (SIR), SAVE, etc. Many methods such as SIR, SAVE, etc. usually put the same weight on each observation to estimate central subspace (CS). By introducing a weight function, WVE puts different weights on different observations according to distance of observations from CS. The weight function makes WVE have very good performance in general and complicated situations, for example, the distribution of regressor deviating severely from elliptical distribution which is the base of many methods, such as SIR, etc. And compared with many existing methods, WVE is insensitive to the distribution of the regressor. The consistency of the WVE is established. Simulations to compare the performances of WVE with other existing methods confirm the advantage of WVE.

  3. Performance of solid state supercapacitors based on polymer electrolytes containing different ionic liquids

    Science.gov (United States)

    Tiruye, Girum Ayalneh; Muñoz-Torrero, David; Palma, Jesus; Anderson, Marc; Marcilla, Rebeca

    2016-09-01

    Four Ionic Liquid based Polymer Electrolytes (IL-b-PE) were prepared by blending a Polymeric Ionic Liquid, Poly(diallyldimethylammonium) bis(trifluoromethanesulfonyl)imide (PILTFSI), with four different ionic liquids: 1-butyl-1-methylpyrrolidinium bis(trifluoromethanesulfonyl)imide (PYR14TFSI) (IL-b-PE1), 1-butyl-1-methylpyrrolidinium bis(fluorosulfonyl)imide (PYR14FSI) (IL-b-PE2), 1-(2-hydroxy ethyl)-3-methylimidazolium bis(trifluoromethylsulfonyl)imide (HEMimTFSI) (IL-b-PE3), and 1-Butyl-1-methylpyrrolidinium dicyanamide, (PYR14DCA) (IL-b-PE4). Physicochemical properties of IL-b-PE such as ionic conductivity, thermal and electrochemical stability were found to be dependent on the IL properties. For instance, ionic conductivity was significantly higher for IL-b-PE2 and IL-b-PE4 containing IL with small size anions (FSI and DCA) than IL-b-PE1 and IL-b-PE3 bearing IL with bigger anion (TFSI). On the other hand, wider electrochemical stability window (ESW) was found for IL-b-PE1 and IL-b-PE2 having ILs with electrochemically stable pyrrolidinium cation and FSI and TFSI anions. Solid state Supercapacitors (SCs) were assembled with activated carbon electrodes and their electrochemical performance was correlated with the polymer electrolyte properties. Best performance was obtained with SC having IL-b-PE2 that exhibited a good compromise between ionic conductivity and electrochemical window. Specific capacitance (Cam), real energy (Ereal) & real power densities (Preal) as high as 150 F g-1, 36 Wh kg-1 & 1170 W kg-1 were found at operating voltage of 3.5 V.

  4. Conductivity studies of biopolymer electrolytes based on chitosan incorporated with NH4Br

    International Nuclear Information System (INIS)

    A polymer electrolyte system based on chitosan complexed with ammonium bromide (NH4Br) salt was prepared by the solution cast technique. 30 wt% NH4Br added electrolyte gave a room temperature conductivity of (4.38 ± 1.26) × 10−7 S cm−1 and increased to (2.15 ± 0.47) × 10−4 S cm−1 with addition of 40 wt% glycerol. The dependence of the conductivity on temperature proves that both chitosan–NH4Br and chitosan–NH4Br–glycerol systems are Arrhenian. The activation energy (Ea) value for 70 wt% chitosan–30 wt% NH4Br film is 0.31 eV and the Ea value for 42 wt% chitosan–18 wt% NH4Br–40 wt% glycerol film is 0.20 eV. The carboxamide band at 1640 cm−1 and the amine band at 1549 cm−1 in the spectrum of pure chitosan film shifted to 1617 and 1516 cm−1, respectively, in the spectrum of 70 wt% chitosan–30 wt% NH4Br film, indicating the occurrence of complexation between polymer and salt. The band at 1024 cm−1 in the pure chitosan film spectrum, which corresponds to the C–O stretching vibration, shifted to lower wavenumbers on addition of salt. A new band appears at 997 cm−1 on addition of 40 wt% glycerol. (paper)

  5. Searching for electrolytes and electrodes for CO2 reduction below 300 °C

    DEFF Research Database (Denmark)

    Vico, Federica

    conducted at Stanford University – Chemical Engineer Department, where it was possible to utilize an experimental setup which ensures high sensitivity for minor products from the CO2 reduction reaction. Seven products were identified with the copper foam electrode tested to -0.98 V vs. RHE. H2, formate...

  6. Electrolytic reduction of mixed solid oxides in molten salts for energy efficient production of the TiNi alloy

    Institute of Scientific and Technical Information of China (English)

    ZHU Yong; MA Meng; WANG Dihua; JIANG Kai; HU Xiaohong; JIN Xianbo; George Z. CHEN

    2006-01-01

    Direct electrochemical reduction of mixed TiO2 and NiO powders to TiNi alloy has been successfully demonstrated in molten CaCl2 at 900℃ by constant voltage electrolysis. The electrolysis energy consumption was as low as 23.4 kWh/kg-TiNi,although the current efficiency was 20.5% in the preliminary experiments. During the process, NiO was first reduced to Ni at high speed, accompanied by TiO2 being perovskitized to CaTiO3-x which was gradually reduced to Ni3Ti and TiNi, assisted by the depolarization of the preformed Ni. The cell voltage for preparation of the TiNi alloy was lower than that for Ti. Adjusting the cell voltage not only affected the reduction speed, but also offered a convenient access to the preparation of the nickel/perovskite composite.

  7. Separators for Li-Ion and Li-Metal Battery Including Ionic Liquid Based Electrolytes Based on the TFSI− and FSI− Anions

    Directory of Open Access Journals (Sweden)

    Marija Kirchhöfer

    2014-08-01

    Full Text Available The characterization of separators for Li-ion or Li-metal batteries incorporating hydrophobic ionic liquid electrolytes is reported herein. Ionic liquids made of N-butyl-N-methylpyrrolidinium (PYR14+ or N-methoxyethyl-N-methylpyrrolidinium (PYR12O1+, paired with bis(trifluoromethanesulfonylimide (TFSI− or bis(fluorosulfonylimide (FSI− anions, were tested in combination with separators having different chemistries and morphologies in terms of wetting behavior, Gurley and McMullin number, as well as Li/(Separator + Electrolyte interfacial properties. It is shown that non-functionalized microporous polyolefin separators are poorly wetted by FSI−-based electrolytes (contrary to TFSI−-based electrolytes, while the ceramic coated separator Separion® allows good wetting with all electrolytes. Furthermore, by comparing the lithium solid electrolyte interphase (SEI resistance evolution at open circuit and during cycling, depending on separator morphologies and chemistries, it is possible to propose a scale for SEI forming properties in the order: PYR12O1FSI > PYR14FSI > PYR14TFSI > PYR12O1TFSI. Finally, the impact the separator morphology is evidenced by the SEI resistance evolution and by comparing Li electrodes cycled using separators with two different morphologies.

  8. Electrical analysis of amorphous corn starch-based polymer electrolyte membranes doped with LiI

    Science.gov (United States)

    Shukur, M. F.; Ibrahim, F. M.; Majid, N. A.; Ithnin, R.; Kadir, M. F. Z.

    2013-08-01

    In this work, polymer electrolytes have been prepared by doping starch with lithium iodide (LiI). The incorporation of 30 wt% LiI optimizes the room temperature conductivity of the electrolyte at (1.83 ± 0.47) × 10-4 S cm-1. Further conductivity enhancement to (9.56 ± 1.19) × 10-4 S cm-1 is obtained with the addition of 30 wt% glycerol. X-ray diffraction analysis indicates that the conductivity enhancement is due to the increase in amorphous content. The activation energy, Ea, of 70 wt% starch-30 wt% LiI electrolyte is 0.26 eV, while 49 wt% starch-21 wt% LiI-30 wt% glycerol electrolyte exhibits an Ea of 0.16 eV. Dielectric studies show that all the electrolytes obey non-Debye behavior. The power law exponent s is obtained from the variation of dielectric loss, ɛi, with frequency at different temperatures. The conduction mechanism of 70 wt% starch-30 wt% LiI electrolyte can be explained by the correlated barrier hopping model, while the conduction mechanism for 49 wt% starch-21 wt% LiI-30 wt% glycerol electrolyte can be represented by the quantum mechanical tunneling model.

  9. Electrical analysis of amorphous corn starch-based polymer electrolyte membranes doped with LiI

    International Nuclear Information System (INIS)

    In this work, polymer electrolytes have been prepared by doping starch with lithium iodide (LiI). The incorporation of 30 wt% LiI optimizes the room temperature conductivity of the electrolyte at (1.83 ± 0.47) × 10−4 S cm−1. Further conductivity enhancement to (9.56 ± 1.19) × 10−4 S cm−1 is obtained with the addition of 30 wt% glycerol. X-ray diffraction analysis indicates that the conductivity enhancement is due to the increase in amorphous content. The activation energy, Ea, of 70 wt% starch–30 wt% LiI electrolyte is 0.26 eV, while 49 wt% starch–21 wt% LiI–30 wt% glycerol electrolyte exhibits an Ea of 0.16 eV. Dielectric studies show that all the electrolytes obey non-Debye behavior. The power law exponent s is obtained from the variation of dielectric loss, εi, with frequency at different temperatures. The conduction mechanism of 70 wt% starch–30 wt% LiI electrolyte can be explained by the correlated barrier hopping model, while the conduction mechanism for 49 wt% starch–21 wt% LiI–30 wt% glycerol electrolyte can be represented by the quantum mechanical tunneling model. (paper)

  10. Platinum-based oxygen reduction electrocatalysts.

    Science.gov (United States)

    Wu, Jianbo; Yang, Hong

    2013-08-20

    An efficient oxygen reduction reaction (ORR) offers the potential for clean energy generation in low-temperature, proton-exchange membrane fuel cells running on hydrogen fuel and air. In the past several years, researchers have developed high-performance electrocatalysts for the ORR to address the obstacles of high cost of the Pt catalyst per kilowatt of output power and of declining catalyst activity over time. Current efforts are focused on new catalyst structures that add a secondary metal to change the d-band center and the surface atomic arrangement of the catalyst, altering the chemisorption of those oxygencontaining species that have the largest impact on the ORR kinetics and improving the catalyst activity and cost effectiveness. This Account reviews recent progress in the design of Pt-based ORR electrocatalysts, including improved understanding of the reaction mechanisms and the development of synthetic methods for producing catalysts with high activity and stability. Researchers have made several types of highly active catalysts, including an extended single crystal surface of Pt and its alloy, bimetallic nanoparticles, and self-supported, low-dimensional nanostructures. We focus on the design and synthetic strategies for ORR catalysts including controlling the shape (or facet) and size of Pt and its bimetallic alloys, and controlling the surface composition and structure of core-shell, monolayer, and hollow porous structures. The strong dependence of ORR performance on facet and size suggests that synthesizing nanocrystals with large, highly reactive {111} facets could be as important, if not more important, to increasing their activity as simply making smaller nanoparticles. A newly developed carbon-monoxide (CO)-assisted reduction method produces Pt bimetallic nanoparticles with controlled facets. This CO-based approach works well to control shapes because of the selective CO binding on different, low-indexed metal surfaces. Post-treatment under

  11. Electrical characterization of proton conducting polymer electrolyte based on bio polymer with acid dopant

    Science.gov (United States)

    Kalaiselvimary, J.; Pradeepa, P.; Sowmya, G.; Edwinraj, S.; Prabhu, M. Ramesh

    2016-05-01

    This study describes the biodegradable acid doped films composed of chitosan and Perchloric acid with different ratios (2.5 wt %, 5 wt %, 7.5 wt %, 10 wt %) was prepared by the solution casting technique. The temperature dependence of the proton conductivity of complex electrolytes obeys the Arrhenius relationship. Proton conductivity of the prepared polymer electrolyte of the bio polymer with acid doped was measured to be approximately 5.90 × 10-4 Scm-1. The dielectric data were analyzed using Complex impedance Z*, Dielectric loss ɛ', Tangent loss for prepared polymer electrolyte membrane with the highest conductivity samples at various temperature.

  12. Novel configuration of poly(vinylidenedifluoride)-based gel polymer electrolyte for application in lithium-ion batteries

    Science.gov (United States)

    Fasciani, Chiara; Panero, Stefania; Hassoun, Jusef; Scrosati, Bruno

    2015-10-01

    Herein we propose a novel poly(vinylidene difluoride) (PVdF)-based gel polymer electrolyte (GPE) for application in lithium-ion batteries, LIBs. The GPE is prepared under air as a dry, flexible film and directly gelled during LIB assembly with a conventional liquid organic electrolyte. The dry-gel here originally reported maintains its structural integrity due to the presence of crystallized EC-solvent within its matrix that avoids structural collapse, as demonstrated by TGA analysis. By avoiding the use of controlled atmosphere, the GPE is easy to handle and suitable for roll-to-roll scaling-up, i.e. characteristics missed by the common gel membranes. Scanning Electron Microscopy (SEM) evidences a micrometric polymer network of the dry membrane precursor acting as the support matrix for the gelation. Electrochemical impedance spectroscopy (EIS) measurements and galvanostatic tests suggest a good stability of the lithium electrode/gel electrolyte interface and a satisfactory lithium transference number. Cycling tests of gel-electrolyte-based lithium half-cells using lithium iron phosphate (LiFePO4, LFP) and graphite (C), respectively, as counter electrodes, as well as of a full C/LFP lithium-ion battery confirm the suitability of the GPE developed in this work for application in stable, low cost and environmentally friendly energy storage systems.

  13. Comparing the rehydration potential of different milk-based drinks to a carbohydrate-electrolyte beverage.

    Science.gov (United States)

    Desbrow, Ben; Jansen, Sarah; Barrett, Abby; Leveritt, Michael D; Irwin, Christopher

    2014-12-01

    The aim of this study was to compare the rehydration potential of a carbohydrate-electrolyte beverage with several varieties of milk following exercise-induced fluid losses. Fifteen male participants (age 24.9 ± 5.5 years, height 179.3 ± 4.9 cm, body mass 75.8 ± 6.6 kg (mean ± SD)) lost 2.0% ± 0.2% body mass through intermittent cycling before consuming a different beverage on 4 separate occasions. Drinks included cow's milk (286 kJ·100 mL(-1)), soy milk (273 kJ·100 mL(-1)), a milk-based liquid meal supplement (Sustagen Sport (Nestle); 417 kJ·100 mL(-1)), and a sports drink (Powerade (Coca Cola Ltd); 129 kJ·100 mL(-1)). Beverages were consumed over 1 h in volumes equivalent to 150% of body mass loss. Body mass, blood and urine samples, and measures of gastrointestinal tolerance were obtained before and hourly for 4 h after beverage consumption. Net body mass at the conclusion of each trial was significantly less with Powerade (-1.37 ± 0.3 kg) than with cow's milk (-0.92 ± 0.48 kg), soy milk (-0.78 ± 0.37 kg), and Sustagen Sport (-0.48 ± 0.39 kg). Net body mass was also significantly greater for Sustagen Sport compared with cow's milk trials, but not soy milk. Upon completion of trials, the percentage of beverage retained was Sustagen Sport 65.1% ± 14.7%, soy milk 46.9% ± 19.9%, cow's milk 40.0% ± 24.9%, and Powerade 16.6% ± 16.5%. Changes in plasma volume and electrolytes were unaffected by drink treatment. Subjective ratings of bloating and fullness were higher during all milk trials compared with Powerade whereas ratings of overall thirst were not different between beverages. Milk-based drinks are more effective rehydration options compared with traditional sports drinks. The additional energy, protein, and sodium in a milk-based liquid meal supplement facilitate superior fluid recovery following exercise.

  14. Facile preparation of polymer electrolytes based on the polymerized ionic liquid poly((4-vinylbenzyl)trimethylammonium bis(trifluoromethanesulfonylimide)) for lithium secondary batteries

    International Nuclear Information System (INIS)

    Graphical abstract: (A) The main components of PIL electrolytes, (B) A PIL electrolyte sample. - Highlights: • A new polymer electrolyte incorporating a DEME-TFSI liquid is prepared. • The ionic conductivity of the electrolytes reaches 7.58 × 10−4 S cm−1 at 60 °C. • Batteries discharge 130 mAh g−1 at 0.1 C rates with good capacity retention. - Abstract: The polymer electrolytes based on a novel poly((4-vinylbenzyl)trimethylammonium bis(trifluoromethanesulfonylimide)) polymeric ionic liquid (PIL) as polymer host and containing DEME-TFSI ionic liquid, LiTFSI salt and nano silica are prepared. The polymer electrolyte is chemically stable even at a higher temperature of 60 °C in contact with lithium anode. Particularly, the electrolyte exhibits high lithium ion conductivity, wide electrochemical stability window and good lithium stripping/plating performance. When the IL content reaches 60% (the weight ratio of DEME-TFSI/PIL), the PIL electrolyte presents a higher ionic conductivity, and it is 7.58 × 10−4 S cm−1 at 60 °C. Preliminary battery tests show that Li/LiFePO4 cells with the PIL electrolytes are capable to deliver above 130 mAh g−1 at 60 °C with very good capacity retention

  15. Sequential sampling designs based on space reduction

    Science.gov (United States)

    Liu, Haitao; Xu, Shengli; Wang, Xiaofang

    2015-07-01

    In the field of engineering design and optimization, metamodels are widely used to replace expensive simulation models in order to reduce computing costs. To improve the accuracy of metamodels effectively and efficiently, sequential sampling designs have been developed. In this article, a sequential sampling design using the Monte Carlo method and space reduction strategy (MCSR) is implemented and discussed in detail. The space reduction strategy not only maintains good sampling properties but also improves the efficiency of the sampling process. Furthermore, a local boundary search (LBS) algorithm is proposed to efficiently improve the performance of MCSR, which is called LBS-MCSR. Comparative results with several sequential sampling approaches from low to high dimensions indicate that the space reduction strategy generates samples with better sampling properties (and thus better metamodel accuracy) in less computing time.

  16. Nb-doped TiO2 cathode catalysts for oxygen reduction reaction of polymer electrolyte fuel cells

    KAUST Repository

    Arashi, Takuya

    2014-09-01

    Nb-doped TiO2 particles were studied as electrocatalysts for the oxygen reduction reaction (ORR) under acidic conditions. The Nb-doped TiN nanoparticles were first synthesized by meso-porous C3N4 and then fully oxidized to Nb-doped TiO2 by immersing in 0.1 M H 2SO4 at 353 K for 24 h. Although the ORR activity of the as-obtained sample was low, a H2 treatment at relatively high temperature (1173 K) dramatically improved the ORR performance. An onset potential as high as 0.82 VRHE was measured. No degradation of the catalysts was observed during the oxidation-reduction cycles under the ORR condition for over 127 h. H2 treatment at temperatures above 1173 K caused the formation of a Ti4O7 phase, resulting in a decrease in ORR current. Elemental analysis indicated that the Nb-doped TiO 2 contained 25 wt% residual carbon. Calcination in air at 673 or 973 K eliminated the residual carbon in the catalyst, which was accompanied by a dramatic decrease in ORR activity. This post-calcination process may reduce the conductivity of the sample by filling the oxygen vacancies, and the carbon residue in the particle aggregates may enhance the electrocatalytic activity for ORR. The feasibility of using conductive oxide materials as electrocatalysts is discussed. © 2013 Elsevier B.V.

  17. Crosslinked polymer gel electrolytes based on polyethylene glycol methacrylate and ionic liquid for lithium battery applications

    Energy Technology Data Exchange (ETDEWEB)

    Liao, Chen [ORNL; Sun, Xiao-Guang [ORNL; Dai, Sheng [ORNL

    2013-01-01

    Gel polymer electrolytes were synthesized by copolymerization polyethylene glycol methyl ether methacrylate with polyethylene glycol dimethacrylate in the presence of a room temperature ionic liquid, methylpropylpyrrolidinium bis(trifluoromethanesulfonyl)imide (MPPY TFSI). The physical properties of gel polymer electrolytes were characterized by thermal analysis, impedance spectroscopy, and electrochemical tests. The ionic conductivities of the gel polymer electrolytes increased linearly with the amount of MPPY TFSI and were mainly attributed to the increased ion mobility as evidenced by the decreased glass transition temperatures. Li||LiFePO4 cells were assembled using the gel polymer electrolytes containing 80 wt% MPPY TFSI via an in situ polymerization method. A reversible cell capacity of 90 mAh g 1 was maintained under the current density of C/10 at room temperature, which was increased to 130 mAh g 1 by using a thinner membrane and cycling at 50 C.

  18. Physics Based Electrolytic Capacitor Degradation Models for Prognostic Studies under Thermal Overstress

    Data.gov (United States)

    National Aeronautics and Space Administration — Electrolytic capacitors are used in several applications rang- ing from power supplies on safety critical avionics equipment to power drivers for electro-mechanical...

  19. American Society of Nephrology Quiz and Questionnaire 2015: Electrolytes and Acid-Base Disorders.

    Science.gov (United States)

    Rosner, Mitchell H; Perazella, Mark A; Choi, Michael J

    2016-04-01

    The Nephrology Quiz and Questionnaire remains an extremely popular session for attendees of the annual Kidney Week meeting of the American Society of Nephrology. During the 2015 meeting the conference hall was once again overflowing with eager quiz participants. Topics covered by the experts included electrolyte and acid-base disorders, glomerular disease, end-stage renal disease and dialysis, and kidney transplantation. Complex cases representing each of these categories together with single-best-answer questions were prepared and submitted by the panel of experts. Before the meeting, training program directors of nephrology fellowship programs and nephrology fellows in the United States answered the questions through an internet-based questionnaire. During the live session members of the audience tested their knowledge and judgment on the same series of case-oriented questions in a quiz. The audience compared their answers in real time using a cell-phone app containing the answers of the nephrology fellows and training program directors. The results of the online questionnaire were displayed, and then the quiz answers were discussed. As always, the audience, lecturers, and moderators enjoyed this highly educational session. This article recapitulates the session and reproduces selected content of educational value for theClinical Journal of the American Society of Nephrologyreaders. Enjoy the clinical cases and expert discussions. PMID:26825098

  20. Preparation and characterization of plasticized palm-based polyurethane solid polymer electrolyte

    International Nuclear Information System (INIS)

    Palm-based polyurethane solid polymer electrolyte was prepared via prepolymerization method between palm kernel oil based polyols (PKO-p) and 2,4’-diphenylmethane diisocyanate (2,4’-MDI) in acetone at room temperature with the vary amount of lithium trifuoromethanesulfonate (LiCF3SO3) salt and polyethylene glycol (PEG). The film was analyzed using attenuated total reflection infrared (ATR-IR) spectroscopy, electrochemical impedance spectroscopy (EIS) and X-ray diffractometry (XRD). EIS result indicated ionic conductivity obtained with 30 wt% LiCF3SO3 increased to 6.55 × 10−6 S cm−1 when 10 wt.% of plasticizer was added into the system. FTIR analysis showed the interaction between lithium ions and amine (-N-H) at 3600–3100 cm−1, carbonyl (-C=O) at 1750–1650 cm−1 and ether (-C-O-C-) at 1150–1000 cm−1 of the polyurethane forming polymer-salt complexes. The XRD result confirmed that LiCF3SO3 salt completely dissociated within the polyurethane film with the absence of crystalline peaks of LiCF3SO3

  1. Carbon Cathodes in Rechargeable Lithium-Oxygen Batteries Based on Double-Lithium-Salt Electrolytes.

    Science.gov (United States)

    Yoo, Eunjoo; Zhou, Haoshen

    2016-06-01

    The use of carbon materials as air electrodes in lithium-oxygen (Li-O2 ) batteries is known to be advantageous owing to their good conductivity and because they offer sites suitable for the reversible electrode reactions. However, the exact influence of carbon materials on the electrochemical performance of Li-O2 batteries is not clear. In this study the electrochemical performance of four different types of carbon materials (multiwalled carbon nanotubes (MWCNTs), CMK-3, graphene nanosheets (GNSs), and Ketjen Black (KB)) as air electrodes is examined. We find that a Li-O2 cell based on an electrode of multiwalled carbon nanotubes (MWCNTs) demonstrates good rate performance and cycle stability, when using LiNO3 -LiTFSI/DMSO as electrolyte. Li-O2 cells based on such MWCNT electrodes, with a cut-off capacity of 1000 mAh g(-1) at 500 mA g(-1) , can undergo around 90 cycles without obvious losses of capacity. Even when the discharge depth is increased to 2000 mA h g(-1) , stable cycling is maintained for 45 cycles at a charge potential below 4.0 V. PMID:27120298

  2. Preparation and characterization of plasticized palm-based polyurethane solid polymer electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Daud, Farah Nadia; Ahmad, Azizan; Badri, Khairiah Haji [School of Chemical Science and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600 UKM Bangi, Selangor Darul Ehsan (Malaysia)

    2013-11-27

    Palm-based polyurethane solid polymer electrolyte was prepared via prepolymerization method between palm kernel oil based polyols (PKO-p) and 2,4’-diphenylmethane diisocyanate (2,4’-MDI) in acetone at room temperature with the vary amount of lithium trifuoromethanesulfonate (LiCF{sub 3}SO{sub 3}) salt and polyethylene glycol (PEG). The film was analyzed using attenuated total reflection infrared (ATR-IR) spectroscopy, electrochemical impedance spectroscopy (EIS) and X-ray diffractometry (XRD). EIS result indicated ionic conductivity obtained with 30 wt% LiCF3SO3 increased to 6.55 × 10{sup −6} S cm{sup −1} when 10 wt.% of plasticizer was added into the system. FTIR analysis showed the interaction between lithium ions and amine (-N-H) at 3600–3100 cm{sup −1}, carbonyl (-C=O) at 1750–1650 cm{sup −1} and ether (-C-O-C-) at 1150–1000 cm{sup −1} of the polyurethane forming polymer-salt complexes. The XRD result confirmed that LiCF{sub 3}SO{sub 3} salt completely dissociated within the polyurethane film with the absence of crystalline peaks of LiCF{sub 3}SO{sub 3}.

  3. Fabrication and performance of PEN SOFCs with proton-conducting electrolyte

    Institute of Scientific and Technical Information of China (English)

    ZHONG Li; LUO Jingli

    2007-01-01

    A positive-electrolyte-negative (PEN) assembly solid oxide fuel cell (SOFC) with a thin electrolyte film for intermediate temperature operation was fabricated.Instead of the traditional screen-printing method,both anode and cathode catalysts were pressed simultaneously and formed with the fabrication of nano-composite electrolyte by press method.This design offered some advantageous configurations that diminished ohmic resistance between electrolyte and electrodes.It also increased the proton-conducting rate and improved the performance of SOFCs due to the reduction of membrane thickness and good contact between electrolyte and electrodes.The fabricated PEN cell generated electricity between 600℃ and 680~C using H2S as fuel feed and Ni-S-based composite anode,nano-composite electrolyte (Li2SO4 + Al2O3) film and a NiO-based composite cathode were achieved at 600℃ and 680℃,respectively.

  4. Ionic liquid-based electrolyte with binary lithium salts for high performance lithium-sulfur batteries

    Science.gov (United States)

    Wu, Feng; Zhu, Qizhen; Chen, Renjie; Chen, Nan; Chen, Yan; Ye, Yusheng; Qian, Ji; Li, Li

    2015-11-01

    Rechargeable Li-S batteries have suffered several technical obstacles, such as rapid capacity fading and low coulombic efficiency. To overcome these problems, we design new electrolytes containing N-methoxyethyl-N-methylpyrrolidinium bis(trifluoromethanesulfonyl)-imide (Pyr1,2O1TFSI) and tri(ethylene glycol)dimethyl ether (TEGDME) in mass ratio of 7:3. Moreover, Lithium difluoro(oxalate)borate (LiODFB) is introduced for the modification. Although the addition of LiODFB as additive lead to extremely high viscosity of electrolyte and inferior performance of the cells, the electrolyte containing lithium bis(trifluoromethanesulfonyl)imide (LiTFSI, 0.84 nm) and LiODFB (0.60 nm) mixture with a total molar concentration of 0.4 mol kg-1 as binary lithium salt shows excellent electrochemical performance. The Pyr1,2O1TFSI/TEGDME electrolyte with LiTFSI/LiODFB binary lithium salts in mole ratio of 6:4 is obtained after optimizing ratio. The Li-S cells containing this electrolyte system show excellent capacity and cycle performance, whose initial discharge capacity is 1264.4 mAh g-1, and retains 911.4 mAh g-1 after 50 cycles with the coulombic efficiency more than 95%. It can be attributed the solid-electrolyte interphase (SEI)-forming ability of LiODFB which protect Li anode from suffering lithium dendrites and prevent the shuttle phenomenon. The novel electrolytes provide good cycling stability and high coulombic efficiency for the Li-S batteries, which is suggested as a promising electrolyte for Li-S batteries.

  5. Activity Coefficient Derivatives of Ternary Systems Based on Scatchard's Neutral Electrolyte description

    Energy Technology Data Exchange (ETDEWEB)

    Miller, D G

    2007-05-16

    Activity coefficient derivatives with respect to molality are presented for the Scatchard Neutral Electrolyte description of a ternary common-ion electrolyte system. These quantities are needed for the calculation of 'diffusion Onsager coefficients' and in turn for tests of the Onsager Reciprocal Relations in diffusion. The usually-omitted b{sub 23} term is included. The direct SNE binary approximations and a further approximation are discussed. Binary evaluation strategies other than constant ionic strength are considered.

  6. Solid Polymer Electrolytes Based on Cross-linkable Oligo (oxyethylene)-Branched Oligo (organophosphazenes)

    Institute of Scientific and Technical Information of China (English)

    Shuhua Zhou; Shibi Fang

    2005-01-01

    @@ 1Introduction Solid polymer electrolytes have attracted considerable interest because of their potential application in secondary high energy density lithium batteries. The poly(ethylene oxide)(PEO) has been widely studied as the classical polymer matrix for solid polymer electrolytes. However, the poor room temperature conductivity due to its crystalline is the principal problem to be overcomed. This has prompted many researchers to attempt to modify the properties of PEO.

  7. Fluoroethylene Carbonate Addition Effect on Electrochemical Properties of Mixed Carbonate-based Organic Electrolyte Solution for a Capacitor

    Energy Technology Data Exchange (ETDEWEB)

    Kim, Mingyeong; Kim, Seok [Pusan National Univ., Busan (Korea, Republic of); Kim, Ickjun; Yang, Sunhye [Korea Electrotechnology Research Institute, Changwon (Korea, Republic of)

    2014-02-15

    In this paper, organic solvent electrolytes were prepared by a mixture of propylene carbonate (PC), dimethyl carbonate (DMC), tetraethylammonium tetrafluoroborate (TEABF{sub 4}) as a salt, and by containing a different content of fluoroethylene carbonate (FEC) as an additive agenT{sup -} The aim of this paper is to evaluate the ionic properties of propylene carbonate (PC)/dimethyl carbonate (DMC) mixtures as solvents for a capacitor application, in view of improving the electrochemical performances. The bulk resistance and interfacial resistance of the mixture electrolytes were investigated using an AC impedance method. The morphology of carbon-based electrodes which were contained in different electrolytes was analyzed by scanning electron microscopy (SEM) method. From the experimental results, by increasing the FEC content, capacitance of electrodes was increased, and the interfacial resistance was decreased. In particular, by a content of 2 vol % FEC in 0.2 M TEABF{sub 4} PC/DMC solvent, the electrolyte showed the superior capacitance. However, when FEC content exceeds 2 vol %, the capacitance was decreased and the interfacial resistance was increased.

  8. Interaction of High Flash Point Electrolytes and PE-Based Separators for Li-Ion Batteries

    Directory of Open Access Journals (Sweden)

    Andreas Hofmann

    2015-08-01

    Full Text Available In this study, promising electrolytes for use in Li-ion batteries are studied in terms of interacting and wetting polyethylene (PE and particle-coated PE separators. The electrolytes are characterized according to their physicochemical properties, where the flow characteristics and the surface tension are of particular interest for electrolyte–separator interactions. The viscosity of the electrolytes is determined to be in a range of η = 4–400 mPa∙s and surface tension is finely graduated in a range of γL = 23.3–38.1 mN∙m−1. It is verified that the technique of drop shape analysis can only be used in a limited matter to prove the interaction, uptake and penetration of electrolytes by separators. Cell testing of Li|NMC half cells reveals that those cell results cannot be inevitably deduced from physicochemical electrolyte properties as well as contact angle analysis. On the other hand, techniques are more suitable which detect liquid penetration into the interior of the separator. It is expected that the results can help fundamental researchers as well as users of novel electrolytes in current-day Li-ion battery technologies for developing and using novel material combinations.

  9. A fuel cell operating between room temperature and 250 °C based on a new phosphoric acid based composite electrolyte

    Science.gov (United States)

    Lan, Rong; Xu, Xiaoxiang; Tao, Shanwen; Irvine, John T. S.

    A phosphoric acid based composite material with core-shell microstructure has been developed to be used as a new electrolyte for fuel cells. A fuel cell based on this electrolyte can operate at room temperature indicating leaching of H 3PO 4 with liquid water is insignificant at room temperature. This will help to improve the thermal cyclability of phosphoric acid based electrolyte to make it easier for practical use. The conductivity of this H 3PO 4-based electrolyte is stable at 250 °C with addition of the hydrophilic inorganic compound BPO 4 forming a core-shell microstructure which makes it possible to run a PAFC at a temperature above 200 °C. The core-shell microstructure retains after the fuel cell measurements. A power density of 350 mW/cm 2 for a H 2/O 2 fuel cell has been achieved at 200 °C. The increase in operating temperature does not have significant benefit to the performance of a H 2/O 2 fuel cell. For the first time, a composite electrolyte material for phosphoric acid fuel cells which can operate in a wide range of temperature has been evaluated but certainly further investigation is required.

  10. SISGR: Improved Electrical Energy Storage with Electrochemical Double Layer Capacitance Based on Novel Carbon Electrodes, New Electrolytes, and Thorough Development of a Strong Science Base

    Energy Technology Data Exchange (ETDEWEB)

    Ruoff, Rodney S. [PI; Alam, Todd M. [co-PI; Bielawski, Christopher W. [co-PI; Chabal, Yves [co-PI; Hwang, Gyeong [co-PI; Ishii, Yoshitaka [co-PI; Rogers, Robin [co-PI

    2014-07-23

    The broad objective of the SISGR program is to advance the fundamental scientific understanding of electrochemical double layer capacitance (EDLC) and thus of ultracapacitor systems composed of a new type of electrode based on chemically modified graphene (CMG) and (primarily) with ionic liquids (ILs) as the electrolyte. Our team has studied the interplay between graphene-based and graphene-derived carbons as the electrode materials in electrochemical double layer capacitors (EDLC) systems on the one hand, and electrolytes including novel ionic liquids (ILs), on the other, based on prior work on the subject.

  11. PVDF-Based Micro Inorganic Fillers-Containing Polymer Electrolyte Membranes

    Institute of Scientific and Technical Information of China (English)

    BAI Ying; WU Feng; WU Chuan

    2006-01-01

    Polymer electrolyte membranes based on poly (vinylidene fluoride-co-hexafluoropropylene) (PVDFHFP) with and without different types of micro inorganic fillers were prepared by phase-inversion process.Morphologies, porosities and electrochemical properties of the as-prepared membranes were investigated by means of scanning electronic microscopy (SEM), PC (propylene carbonate) uptake and alternating current(AC) impedance technique. Compared with other membranes, the membrane with micro SiO2 filler shows a dense morphology so that its PC uptake is the highest, namely, 339%. The membrane filled with micro TiO2exhibits good electrochemical performances: the ion conductivity is as high as 1.1 × 10-3 S/cm at 18 ℃,which can meet the demand of lithium ion batteries. Moreover, its initial charge-discharge efficiency exceeds89 %. The composite membranes with micro SiO2, TiO2 and A12O3 are more suitable for the utilization in lithium ion batteries due to better cycleability, whereas the battery assembled with the blank membrane containing no inorganic fillers encounters a short circuit after the 5th cycle.

  12. Conductivity and transport studies of plasticized chitosan-based proton conducting biopolymer electrolytes

    International Nuclear Information System (INIS)

    This paper focuses on the conductivity and transport properties of chitosan-based solid biopolymer electrolytes containing ammonium thiocyanate (NH4SCN). The sample containing 40 wt% NH4SCN exhibited the highest conductivity value of (1.81 ± 0.50) × 10−4 S cm−1 at room temperature. Conductivity has increased to (1.51 ± 0.12) × 10−3 S cm−1 with the addition of 25 wt% glycerol. The temperature dependence of conductivity for both salted and plasticized systems obeyed the Arrhenius rule. The activation energy (Ea) was calculated for both systems and it is found that the sample with 40 wt% NH4SCN in the salted system obtained an Ea value of 0.148 eV and that for the sample containing 25 wt% glycerol in the plasticized system is 0.139 eV. From the Fourier transform infrared studies, carboxamide and amine bands shifted to lower wavenumbers, indicating that chitosan has interacted with NH4SCN salt. Changes in the C–O stretching vibration band intensity are observed at 1067 cm−1 with the addition of glycerol. The Rice and Roth model was used to explain the transport properties of the salted and plasticized systems. (paper)

  13. Kidney injury, fluid, electrolyte and acid-base abnormalities in alcoholics

    Directory of Open Access Journals (Sweden)

    Adebayo Adewale

    2014-01-01

    Full Text Available In the 21 st century, alcoholism and the consequences of ethyl alcohol abuse are major public health concerns in the United States, affecting approximately 14 million people. Pertinent to the global impact of alcoholism is the World Health Organisation estimate that 140 million people worldwide suffer from alcohol dependence. Alcoholism and alcohol abuse are the third leading causes of preventable death in the United States. Alcohol dependence and alcohol abuse cost the United State an estimated US$220 billion in 2005, eclipsing the expense associated with cancer (US$196 billion or obesity (US$133 billion. Orally ingested ethyl alcohol is absorbed rapidly without chemical change from the stomach and intestine, reaching maximum blood concentration in about an hour. Alcohol crosses capillary membranes by simple diffusion, affecting almost every organ system in the body by impacting a wide range of cellular functions. Alcohol causes metabolic derangements either directly, via its chemical by-product or secondarily through alcohol-induced disorders. Many of these alcohol-related metabolic disturbances are increased in severity by the malnutrition that is common in those with chronic alcoholism. This review focuses on the acute and chronic injurious consequences of alcohol ingestion on the kidney, as well as the fluid, electrolyte and acid-base abnormalities associated with acute and chronic ingestion of alcohol.

  14. Numerical evaluation of crack growth in polymer electrolyte fuel cell membranes based on plastically dissipated energy

    Science.gov (United States)

    Ding, Guoliang; Santare, Michael H.; Karlsson, Anette M.; Kusoglu, Ahmet

    2016-06-01

    Understanding the mechanisms of growth of defects in polymer electrolyte membrane (PEM) fuel cells is essential for improving cell longevity. Characterizing the crack growth in PEM fuel cell membrane under relative humidity (RH) cycling is an important step towards establishing strategies essential for developing more durable membrane electrode assemblies (MEA). In this study, a crack propagation criterion based on plastically dissipated energy is investigated numerically. The accumulation of plastically dissipated energy under cyclical RH loading ahead of the crack tip is calculated and compared to a critical value, presumed to be a material parameter. Once the accumulation reaches the critical value, the crack propagates via a node release algorithm. From the literature, it is well established experimentally that membranes reinforced with expanded polytetrafluoroethylene (ePTFE) reinforced perfluorosulfonic acid (PFSA) have better durability than unreinforced membranes, and through-thickness cracks are generally found under the flow channel regions but not land regions in unreinforced PFSA membranes. We show that the proposed plastically dissipated energy criterion captures these experimental observations and provides a framework for investigating failure mechanisms in ionomer membranes subjected to similar environmental loads.

  15. Development of structural materials to enable the electrochemical reduction of spent oxide nuclear fuel in a molten salt electrolyte

    International Nuclear Information System (INIS)

    For the development of the advanced spent fuel management process based on the molten salt technology, it is essential to choose the optimum material for the process equipment handling a molten salt. In this study, corrosion behavior of Fe-base superalloy, Ni-base superalloy, non-metallic material and surface modified superalloy were investigated in the hot molten salt under oxidation atmosphere. These experimental data will suggest a guideline for the selection of corrosion resistant materials and help to find the operation criteria of each equipment in aspects of high temperature characteristics and corrosion retardation

  16. Electrolyte materials - Issues and challenges

    Energy Technology Data Exchange (ETDEWEB)

    Balbuena, Perla B. [Department of Chemical Engineering, and Department of Materials Science and Engineering, Texas A and M University, College Station, Texas, 77843 (United States)

    2014-06-16

    Electrolytes are vital components of an electrochemical energy storage device. They are usually composed of a solvent or mixture of solvents and a salt or a mixture of salts which provide the appropriate environment for ionic conduction. One of the main issues associated with the selection of a proper electrolyte is that its electronic properties have to be such that allow a wide electrochemical window - defined as the voltage range in which the electrolyte is not oxidized or reduced - suitable to the battery operating voltage. In addition, electrolytes must have high ionic conductivity and negligible electronic conductivity, be chemically stable with respect to the other battery components, have low flammability, and low cost. Weak stability of the electrolyte against oxidation or reduction leads to the formation of a solid-electrolyte interphase (SEI) layer at the surface of the cathode and anode respectively. Depending on the materials of the electrolyte and those of the electrode, the SEI layer may be composed by combinations of organic and inorganic species, and it may exert a passivating role. In this paper we discuss the current status of knowledge about electrolyte materials, including non-aqueous liquids, ionic liquids, solid ceramic and polymer electrolytes. We also review the basic knowledge about the SEI layer formation, and challenges for a rational design of stable electrolytes.

  17. Catalytic activity of Pt anchored onto graphite nanofiber-poly (3,4-ethylenedioxythiophene) composite toward oxygen reduction reaction in polymer electrolyte fuel cells

    International Nuclear Information System (INIS)

    Highlights: • GNF–PEDOT is explored as a catalyst support for PEFCs. • PEDOT bridges the Pt nanoparticles with GNF via π–π interaction. • Binding strength between Pt and GNF is improved and hence mitigates Pt aggregation. • GNF–PEDOT composite enhances ORR activity and durability in fuel cells. -- Abstract: The potential of graphite nanofiber (GNF)–Poly(3,4-ethylenedioxythiophene) (PEDOT) composite is explored as a catalyst support for polymer electrolyte fuel cells (PEFCs). Due to electron accepting nature of GNF and electron donating nature of PEDOT, the monomer EDOT adsorbs on the surface of GNF due to strong electrostatic π–π interaction. Pt nanoparticles are impregnated on GNF–PEDOT composite by ethylene glycol reduction method and their effects on electro catalytic activity for oxygen reduction reaction (ORR) are systemically studied. Pt particles supported on GNF–PEDOT with catalyst loading of 0.2 mg cm−2 exhibit a peak power density of 537 mW cm−2 at a load current density of 1120 mA cm−2, while it was only 338 mW cm−2 at a load current density of 720 mA cm−2 in case of Pt particles supported on pristine GNF. The superior behavior of GNF–PEDOT supported Pt catalyst could be exclusively credited to the high graphitic nature of GNF and their mild functionalization with PEDOT increasing uniform dispersion of Pt. Indeed, the non-destructive functionalization of GNF with conducting polymer, such as PEDOT, makes them promising catalyst-supports for PEFCs

  18. Elucidating the higher stability of vanadium(V) cations in mixed acid based redox flow battery electrolytes

    Science.gov (United States)

    Vijayakumar, M.; Wang, Wei; Nie, Zimin; Sprenkle, Vincent; Hu, JianZhi

    2013-11-01

    The vanadium(V) cation structures in mixed acid based electrolyte solution were analyzed by density functional theory (DFT) based computational modeling and 51V and 35Cl nuclear magnetic resonance (NMR) spectroscopy. The vanadium(V) cation exists as di-nuclear [V2O3Cl2·6H2O]2+ compound at higher vanadium concentrations (≥1.75 M). In particular, at high temperatures (>295 K) this di-nuclear compound undergoes ligand exchange process with nearby solvent chlorine molecule and forms chlorine bonded [V2O3Cl·6H2O]2+ compound. This chlorine bonded [V2O3Cl2·6H2O]2+ compound might be resistant to the de-protonation reaction which is the initial step in the precipitation reaction in vanadium based electrolyte solutions. The combined theoretical and experimental approach reveals that formation of chlorine bonded [V2O3Cl2·6H2O]2+ compound might be central to the observed higher thermal stability of mixed acid based vanadium(V) electrolyte solutions.

  19. A composite membrane based on a biocompatible cellulose as a host of gel polymer electrolyte for lithium ion batteries

    Science.gov (United States)

    Xiao, S. Y.; Yang, Y. Q.; Li, M. X.; Wang, F. X.; Chang, Z.; Wu, Y. P.; Liu, X.

    2014-12-01

    A composite polymer membrane is prepared by coating poly(vinylidene fluoride) (PVDF) on the surface of a membrane based on methyl cellulose (MC) which is environmentally friendly and cheap. Its characteristics are investigated by scanning electron microscopy, FT-IR, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC). The outer PVDF layers are porous which results in high electrolyte uptake and the lithium ion transference number is much larger than that of the pure MC. Moreover, the cell based on Li//LiFePO4 delivers high discharge capacity and good rate behavior in the range of 4.2-2.5 V when the composite membrane is used as the separator and the host of a gel polymer electrolyte, lithium as the counter and reference electrode, and LiFePO4 as cathode. The obtained results suggest that this unique composite membrane shows great attraction in the lithium ion batteries with high safety and low cost.

  20. New Polymer Electrolyte Membranes Based on Acid Doped PBI For Fuel Cells Operating above 100°C

    DEFF Research Database (Denmark)

    Li, Qingfeng

    2003-01-01

    The technical achievement and challenges for the PEMFC technology based on perfluorosulfonic acid (PFSA) polymer membranes (e.g. Nafion®) are briefly discussed. The newest development for alternative polymer electrolytes for operation above 100°C. As one of the successful approaches to high opera...... operational temperatures, the development and evaluation of acid doped PBI membranes are reviewed, covering polymer synthesis, membrane casting, acid doping, physiochemical characterization and fuel cell tests.......The technical achievement and challenges for the PEMFC technology based on perfluorosulfonic acid (PFSA) polymer membranes (e.g. Nafion®) are briefly discussed. The newest development for alternative polymer electrolytes for operation above 100°C. As one of the successful approaches to high...

  1. Influence of the NiO nanoparticles on the ionic conductivity of the agar-based electrolyte

    Directory of Open Access Journals (Sweden)

    Dalal Jaber Suliman Abdullah Audeh

    2014-01-01

    Full Text Available NiO nanoparticles with an average size of 15 nm were prepared by a simple, reproducible and low-cost controlled method, using nickel nitrate hexahydrate (Ni(NO32·6H2O. These nanoparticles were added to an agar-based polymer electrolyte formula, resulting, after reflux and solution casting, in a proton conducting membrane. The highest ionic conductivity values of 5.19x10-5 S cm-1 at room temperature and 3.32x10-4 S cm-1 at 80 ºC, were obtained for the sample with 50 wt. % of acetic acid and 0.25 g of NiO. Moreover, the samples showed 75 % of transparency in the visible region, a homogeneous surface and mainly amorphous structure. All the obtained results suggest that agar-based polymer electrolyte with NiO nanoparticles are promising candidates for electrochemical devices application.

  2. A Method of Attribute Reduction Based on Rough Set

    Institute of Scientific and Technical Information of China (English)

    LI Chang-biao; SONG Jian-ping

    2005-01-01

    The logging attribute optimization is an important task in the well-logging interpretation.A method of attribute reduction is presented based on rough set. Firstly, the core information of the sample by a general reductive method is determined. Then, the significance of dispensable attribute in the reduction-table is calculated. Finally, the minimum relative reduction set is achieved. The typical calculation and quantitative computation of reservoir parameter in oil logging show that the method of attribute reduction is greatly effective and feasible in logging interpretation.

  3. Printable electrolytes based on polyacrylonitrile and gamma-butyrolactone for dye-sensitized solar cell application

    Science.gov (United States)

    Venkatesan, Shanmugam; Su, Song-Chuan; Hung, Wei-Ning; Liu, I.-Ping; Teng, Hsisheng; Lee, Yuh-Lang

    2015-12-01

    Printable electrolytes for dye-sensitized solar cells (DSSCs) are prepared using a low volatile solvent, gamma-butyrolactone (gBL). Various polymers including polyvinyl acetate (PVA), polyacrylonotrile (PAN), and poly(acrylonitrile-co-vinylacetate) (PAN-VA) are used to regulate the viscosity of the electrolytes. The results show that PAN is the best polymer interms of viscosity, conductivity, and performance of the DSSCs. Increasing the concentration of PAN increases the viscosity of the electrolyte paste, which is advantageous to the operation of a printing process but decreases the electrolyte conductivity and cell performance. This drawback can be compensated by introducing of TiO2 or TiC nanofillers. The quasi-solid-state DSSC prepared using a printing process achieves a conversion efficiency (7.85%) similar to that of the corresponding liquid cell (7.87%). The stability test shows that the presence of TiO2 nanofillers triggers a gradual desorption of dye, decreasing DSSC performance. However, this problem does not appear for the electrolyte using TiC nanofillers, with cell efficiency retaining 96% of its initial value after a 500 h test.

  4. Polymer Electrolytes Based on Electrospun PEO-P(VdF-HFP) Blends for Lithium-Polymer Batteries

    Institute of Scientific and Technical Information of China (English)

    P.Raghvan; J.Manuel; G.Cheruvally; J.H.Ahn

    2007-01-01

    1 Results Electrospinning has attracted immense attention recently as a versatile and easy method to prepare polymer membranes that are made up of thin fibers of micron and sub-micron diameters.Such membranes are particularly suitable as host matrices for polymer electrolytes (PEs) since the interlaying of fibers generate large porosity with fully interconnected pore structure facilitating the easy transport of ions.Characterization of PEs based on electrospun membranes of poly(vinylidene fluoride) (PVd...

  5. Porous dendritic copper: an electrocatalyst for highly selective CO 2 reduction to formate in water/ ionic liquid electrolyte

    OpenAIRE

    Huan, Tran Ngoc; Simon, Philippe; Rousse, Gwenaëlle; Génois, Isabelle; Artero, Vincent; Fontecave, Marc

    2016-01-01

    International audience; Copper is currently extensively studied because it provides promising electrodes for carbon dioxide electroreduction. The original combination, reported here, of a nanostructured porous dendritic Cu-based material, characterized by electron microcopy (SEM, TEM) and X-ray diffraction methods, and a water/ionic liquid mixture as the solvent, contributing to CO 2 solubilization and activation, results in a remarkably efficient (large current densities at low overpotential...

  6. Some Lewis acid-base adducts involving boron trifluoride as electrolyte additives for lithium ion cells

    Science.gov (United States)

    Nie, Mengyun; Madec, L.; Xia, J.; Hall, D. S.; Dahn, J. R.

    2016-10-01

    Three complexes with boron trifluoride (BF3) as the Lewis acid and different Lewis bases were synthesized and used as electrolyte additives in Li[Ni1/3Mn1/3Co1/3]O2/graphite and Li[Ni0.42Mn0.42Co0.16]O2/graphite pouch cells. Lewis acid-base adducts with a boron-oxygen (Bsbnd O) bond were trimethyl phosphate boron trifluoride (TMP-BF) and triphenyl phosphine oxide boron trifluoride (TPPO-BF). These were compared to pyridine boron trifluoride (PBF) which has a boron-nitrogen (Bsbnd N) bond. The experimental results showed that cells with PBF had the least voltage drop during storage at 4.2 V, 4.4 V and 4.7 V at 40 °C and the best capacity retention during long-term cycling at 55 °C compared to cells with the other additives. Charge-hold-discharge cycling combined with simultaneous electrochemical impedance spectroscopy measurements showed that impedance growth in TMP-BF and TPPO-BF containing cells was faster than cells containing 2%PBF, suggesting that PBF is useful for impedance control at high voltages (>4.4 V). XPS analysis of the SEI films highlighted a specific reactivity of the PBF-derived SEI species that apparently hinders the degradation of both LiPF6 and solvent during formation and charge-hold-discharge cycling. The modified SEI films may explain the improved impedance, the smaller voltage drop during storage and the improved capacity retention during cycling of cells containing the PBF additive.

  7. Scale-up of a high temperature polymer electrolyte membrane fuel cell based on polybenzimidazole

    Science.gov (United States)

    Pinar, F. Javier; Cañizares, Pablo; Rodrigo, Manuel A.; Úbeda, Diego; Lobato, Justo

    A high temperature PEM fuel cell stack with a total active area 150 cm 2 has been studied. The PEM technology is based on a polybenzimidazole (PBI) membrane. Cast from a PBI polymer synthesised in our lab, the performance of a three-cell stack was analysed in static and dynamic modes. In static mode, operating at high constant oxygen flow rate (QO2 > 1105 ml O2 / min) produces a small decrease on the stack performance. High constant oxygen stoichiometry (λO2 > 3) does not produce a decrease on the performance of the stack. There are not differences between operating at constant flow rate of oxygen and constant stoichiometry of oxygen in the stack performance. The effect of operating at high temperature with a pressurization system and operating at higher temperatures are beneficial since the performance of the fuel cell is enhanced. A large shut-down stage produces important performance losses due to the loss of catalyst activity and the loss of membrane conductivity. After 150 h of operation at 0.2 A cm -2, it is observed a very high voltage drop. The phosphoric acid leached from the stack was also evaluated and did not exceed 2% (w/w). This fact suggests that the main degradation mechanism of a fuel cell stack based on polybenzimidazole is not the electrolyte loss. In dynamic test mode, it was observed a rapid response of power and current output even at the lower step-time (10 s). In the static mode at 125 °C and 1 atm, the stack reached a power density peak of 0.29 W cm -2 (43.5 W) at 1 V.

  8. An Electrochemical NO₂ Sensor Based on Ionic Liquid: Influence of the Morphology of the Polymer Electrolyte on Sensor Sensitivity.

    Science.gov (United States)

    Kuberský, Petr; Altšmíd, Jakub; Hamáček, Aleš; Nešpůrek, Stanislav; Zmeškal, Oldřich

    2015-11-11

    A systematic study was carried out to investigate the effect of ionic liquid in solid polymer electrolyte (SPE) and its layer morphology on the characteristics of an electrochemical amperometric nitrogen dioxide sensor. Five different ionic liquids were immobilized into a solid polymer electrolyte and key sensor parameters (sensitivity, response/recovery times, hysteresis and limit of detection) were characterized. The study revealed that the sensor based on 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl)imide ([EMIM][N(Tf)2]) showed the best sensitivity, fast response/recovery times, and low sensor response hysteresis. The working electrode, deposited from water-based carbon nanotube ink, was prepared by aerosol-jet printing technology. It was observed that the thermal treatment and crystallinity of poly(vinylidene fluoride) (PVDF) in the solid polymer electrolyte influenced the sensitivity. Picture analysis of the morphology of the SPE layer based on [EMIM][N(Tf)2] ionic liquid treated under different conditions suggests that the sensor sensitivity strongly depends on the fractal dimension of PVDF spherical objects in SPE. Their deformation, e.g., due to crowding, leads to a decrease in sensor sensitivity.

  9. The development of a new type of rechargeable batteries based on hybrid electrolytes.

    Science.gov (United States)

    Zhou, Haoshen; Wang, Yonggang; Li, Huiqiao; He, Ping

    2010-09-24

    Lithium ion batteries (LIBs), which have the highest energy density among all currently available rechargeable batteries, have recently been considered for use in hybrid electric vehicles (HEVs), plug-in hybrid electric vehicles (PHEVs), and pure electric vehicles (PEV). A major challenge in this effort is to increase the energy density of LIBs to satisfy the industrial needs of HEVs, PHEVs, and PEVs. Recently, new types of lithium-air and lithium-copper batteries that employ hybrid electrolytes have attracted significant attention; these batteries are expected to succeed lithium ion batteries as next-generation power sources. Herein, we review the concept of hybrid electrolytes, as well as their advantages and disadvantages. In addition, we examine new battery types that use hybrid electrolytes. PMID:20677207

  10. Heuristic Reduction Algorithm Based on Pairwise Positive Region

    Institute of Scientific and Technical Information of China (English)

    QI Li; LIU Yu-shu

    2007-01-01

    To guarantee the optimal reduct set, a heuristic reduction algorithm is proposed, which considers the distinguishing information between the members of each pair decision classes. Firstly the pairwise positive region is defined, based on which the pairwise significance measure is calculated between the members of each pair classes. Finally the weighted pairwise significance of attribute is used as the attribute reduction criterion, which indicates the necessity of attributes very well. By introducing the noise tolerance factor, the new algorithm can tolerate noise to some extent. Experimental results show the advantages of our novel heuristic reduction algorithm over the traditional attribute dependency based algorithm.

  11. Preparation and characterization of novel solid polymer blend electrolytes based on poly (vinyl pyrrolidone) with various concentrations of lithium perchlorate

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The maximum ionic conductivity value was found to be 0.2307 × 10−5 S cm−1 for PEO(90 wt%)/PVP(10 wt%)/LiClO4(8 wt%) based electrolyte at room temperature. • The structural and functional groups were studied by XRD and FTIR. • Both direct and indirect optical band gap values were evaluated from UV–vis analysis. • The change in viscosity of the polymer electrolytes was studied by photoluminescence spectra. - Abstract: A series of conducting novel solid polymer blend electrolytes (SPE) based on the fixed ratio of poly (ethylene oxide)/poly (vinyl pyrrolidone) (PEO/PVP) and various concentrations of salt lithium perchlorate (LiClO4) were prepared by solvent casting technique. Structural and complex formation of the prepared electrolytes was confirmed by X-ray diffraction and FTIR analyses. The maximum ionic conductivity value was found to be 0.2307 × 10−5 S cm−1 for 8 wt% of LiClO4 based system at ambient temperature. Thermal stability of the present system was studied by thermo gravimetric/differential thermal analysis (TG/DTA). Surface morphology of the sample having maximum ionic conductivity was studied by atomic force microscope (AFM). Optical properties like direct and indirect band gaps were investigated by UV–vis analysis. The change in viscosity of the polymer complexes were also identified using photoluminescence emission spectra. PEO(90)/PVP(10)/LiClO4(8) has the highest conductivity which is supported by the lowest optical band gap and lowest intensity in photoluminescence spectroscopy near 400–450 nm

  12. A Type of Lithium-ion Battery Based on Aqueous electrolyte

    Institute of Scientific and Technical Information of China (English)

    G.J.Wang; N.H.Zhao; L.J.Fu; B.Wang; Y.P.Wu

    2007-01-01

    1 Introduction A new type of rechargeable lithium ion battery with an aqueous electrolyte was announced by W. Li et al. in 1994[1].This type of battery uses the lithium intercalation compounds LiMn2O4 and VO2 as electrode materials and an alkaline aqueous electrolytic solution. By this combination, the disadvantages of the non-aqueous Li-ion battery type, i.e. high cost and safety problems could be faded away[2]. So this type of aqueous Li-ion battery was regarded as the promising power for electric veh...

  13. New-concept Batteries Based on Aqueous Li+/Na+ Mixed-ion Electrolytes

    OpenAIRE

    Liang Chen; Qingwen Gu; Xufeng Zhou; Saixi Lee; Yonggao Xia; Zhaoping Liu

    2013-01-01

    Rechargeable batteries made from low-cost and abundant materials operating in safe aqueous electrolytes are attractive for large-scale energy storage. Sodium-ion battery is considered as a potential alternative of current lithium-ion battery. As sodium-intercalation compounds suitable for aqueous batteries are limited, we adopt a novel concept of Li+/Na+ mixed-ion electrolytes to create two batteries (LiMn2O4/Na0.22MnO2 and Na0.44MnO2/TiP2O7), which relies on two electrochemical processes. On...

  14. Novel Semiconductor-Liquid Heterojunction Solar Cells Based on Cuprous Oxide and Iodine Electrolyte

    International Nuclear Information System (INIS)

    Graphical abstract: Display Omitted -- Highlights: •A novel Cu2O-electrolyte heterojunction solar cell was fabricated on a Cu foil substrate. •The novel solar cell was composed of a Cu2O electrode, electrolyte, and a Pt electrode. •A chemical oxidation method was used to fabricate coral-shaped Cu2O structures. •The influence of various iodine concentrations on device efficiency was studied. -- ABSTRACT: In this study, we report a novel cuprous oxide-electrolyte heterojunction solar cell fabricated on a copper foil substrate. A chemical oxidation method was used to fabricate a cuprous oxide electrode that was then combined with an electrolyte and platinum electrode to form a cuprous oxide-electrolyte heterojunction solar cell. Various analytic technologies were employed to characterize the cuprous oxide electrodes. Scanning electron microscopy (SEM) was employed to observe the surface morphology; energy-dispersive X-ray spectroscopy (EDS), X-ray diffraction (XRD), Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS) were used to characterize the material properties; and ultraviolet-visible (UV-vis) spectroscopy was used to analyze the optical properties of the cuprous oxide. The results show that the particle size of the cuprous oxide ranged from approximately 1–2 μm, which agglomerated and formed coral-shaped structures with lengths and widths of 10–20 and 5–6 μm, respectively, and with absorption wavelengths of 300 to 640 nm. The cuprous oxide-electrolyte heterojunction solar cell was also characterized, and the influence of various iodine (I2) concentrations on device efficiency was studied. The results show that when the I2 concentration of the electrolyte was 10 mM, the short-circuit current density, open-circuit voltage, fill factor, and device conversion efficiency of the cuprous oxide-electrolyte heterojunction solar cell were 3.52 mA/cm2, 0.64 V, 0.32, and 0.72%, respectively

  15. Universal low-temperature MWCNT-COOH-based counter electrode and a new thiolate/disulfide electrolyte system for dye-sensitized solar cells.

    Science.gov (United States)

    Hilmi, Abdulla; Shoker, Tharallah A; Ghaddar, Tarek H

    2014-06-11

    A new thiolate/disulfide organic-based electrolyte system composed of the tetrabutylammonium salt of 2-methyl-5-trifluoromethyl-2H-[1,2,4]triazole-3-thiol (S(-)) and its oxidized form 3,3'-dithiobis(2-methyl-5-trifluoromethyl-2H-[1,2,4]triazole) (DS) has been formulated and used in dye-sensitized solar cells (DSSCs). The electrocatalytic activity of different counter electrodes (CEs) has been evaluated by means of measuring J-V curves, cyclic voltammetry, Tafel plots, and electrochemical impedance spectroscopy. A stable and low-temperature CE based on acid-functionalized multiwalled carbon nanotubes (MWCNT-COOH) was investigated with our S(-)/DS, I(-)/I3(-), T(-)/T2, and Co(II/III)-based electrolyte systems. The proposed CE showed superb electrocatalytic activity toward the regeneration of the different electrolytes. In addition, good stability of solar cell devices based on the reported electrolyte and CE was shown.

  16. All-solid-state lithium-sulfur battery based on a nanoconfined LiBH4 electrolyte

    DEFF Research Database (Denmark)

    Das, Supti; Ngene, Peter; Norby, Poul;

    2016-01-01

    In this work we characterize all-solid-state lithium-sulfur batteries based on nano-confined LiBH4 in mesoporous silica as solid electrolytes. The nano-confined LiBH4 has fast ionic lithium conductivity at room temperature, 0.1 mScm-1, negligible electronic conductivity and its cationic transport...... number (t+ = 0.96), close to unity, demonstrates a purely cationic conductor. The electrolyte has an excellent stability against lithium metal. The behavior of the batteries is studied by cyclic voltammetry and repeated charge/discharge cycles in galvanostatic conditions. The batteries show very good...... performance, delivering high capacities versus sulfur mass, typically 1220 mAhg-1 after 40 cycles at moderate temperature (55°C), 0.03 C rates and working voltage of 2 V....

  17. Liquid electrolyte based on lithium bis-fluorosulfonyl imide salt: Aluminum corrosion studies and lithium ion battery investigations

    Energy Technology Data Exchange (ETDEWEB)

    Abouimrane, A.; Ding, J.; Davidson, I.J. [Institute for Chemical Process and Environmental Technology, National Research Council Canada, 1200 Montreal Road, Ottawa K1A 0R6 (Canada)

    2009-04-01

    The performance of a liquid electrolyte composed of lithium bis-fluorosulfonyl imide (LiSFI) in a 1:1 volume of ethylene carbonate and dimethyl carbonate is evaluated for use in lithium ion batteries. Imide salts offer the benefits of higher thermal stability and could provide a safer alternative to LiPF{sub 6} which is prone to the formation of HF. However, the most studied lithium imide salt, lithium bis(trifluoromethanesulfonyl) imide, is well known to have a problem with corrosion of aluminum which is commonly used as the cathode current collector. Consequently, the corrosion properties of liquid electrolytes based on lithium bis-fluorosulfonyl imide are also investigated. (author)

  18. Exceptional durability enhancement of PA/PBI based polymer electrolyte membrane fuel cells for high temperature operation at 200°C

    DEFF Research Database (Denmark)

    Aili, David; Zhang, Jin; Jakobsen, Mark Tonny Dalsgaard;

    2016-01-01

    The incorporation of phosphotungstic acid functionalized mesoporous silica in phosphoric acid doped polybenzimidazole (PA/PBI) substantially enhances the durability of PA/PBI based polymer electrolyte membrane fuel cells for high temperature operation at 200°C.......The incorporation of phosphotungstic acid functionalized mesoporous silica in phosphoric acid doped polybenzimidazole (PA/PBI) substantially enhances the durability of PA/PBI based polymer electrolyte membrane fuel cells for high temperature operation at 200°C....

  19. Ab initio investigation of ground-states and ionic motion in particular in zirconia-based solid-oxide electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Hirschfeld, Julian Arndt

    2012-12-11

    Electrolytes with high ionic conductivity at lower temperatures are the prerequisite for the success of Solid Oxide Fuel Cells (SOFC). One candidate is doped zirconia. In the past, the electrical resistance of zirconia based SOFC electrolytes has mainly been decreased by reducing its thickness. But there are limits to reducing the thickness and one can say that nowadays the normal ways are basically exhausted to further enhance the conductivity of well-known electrolyte materials. Hence, new approaches need to be found to discover windows of enhanced ionic conductivity. This can be achieved by understanding the quantum-mechanical oxygen transport in unconventional configurations of doped zirconia. Therefore, such an understanding is of fundamental importance. In this thesis two approaches are pursued, the investigation of the strain dependent ionic migration in zirconia based electrolytes and the designing of an electrolyte material structure with enhanced and strongly anisotropic ionic conductivity. The first approach expands the elementary understanding of oxygen migration in oxide lattices. The migration barrier of the oxygen ion jumps in zirconia is determined by applying the Density Functional Theory (DFT) calculations in connection with the Nudged Elastic Band (NEB) method. These computations show an unexpected window of decreased migration barriers at high compressive strains. Similar to other publications a decrease in the migration barrier for expansive strain is observed. But, in addition, a migration barrier decrease under high compressive strains is found beyond a maximal height of the migration barrier. A simple analytic model offers an explanation. The drop of the migration barrier at high compressions originates from the elevation of the ground-state energy. This means: Increasing ground state energies becomes an interesting alternative to facilitate ionic mobility. The second approach is based on the idea, that actually, only in the direction of ion

  20. Artificial Neural Network and Response Surface Methodology Modeling in Ionic Conductivity Predictions of Phthaloylchitosan-Based Gel Polymer Electrolyte

    Directory of Open Access Journals (Sweden)

    Ahmad Danial Azzahari

    2016-01-01

    Full Text Available A gel polymer electrolyte system based on phthaloylchitosan was prepared. The effects of process variables, such as lithium iodide, caesium iodide, and 1-butyl-3-methylimidazolium iodide were investigated using a distance-based ternary mixture experimental design. A comparative approach was made between response surface methodology (RSM and artificial neural network (ANN to predict the ionic conductivity. The predictive capabilities of the two methodologies were compared in terms of coefficient of determination R2 based on the validation data set. It was shown that the developed ANN model had better predictive outcome as compared to the RSM model.

  1. Polyethylene glycol dimethyl ether (PEGDME)-based electrolyte for lithium metal battery

    Science.gov (United States)

    Carbone, Lorenzo; Gobet, Mallory; Peng, Jing; Devany, Matthew; Scrosati, Bruno; Greenbaum, Steve; Hassoun, Jusef

    2015-12-01

    We propose in this work a polyethylene glycol dimethyl ether (MW 500) dissolving lithium trifluoromethansulfonate (LiCF3SO3) salt as suitable electrolyte media for a safe and efficient use of the lithium metal anode in battery. Voltammetry and galvanostatic tests reveal significant enhancement of the electrolyte characteristics, in terms of cycling life and chemical stability, by the addition of lithium nitrate (LiNO3) to the solution. Furthermore, PFG NMR measurements suggest the applicability of the electrolyte in battery in terms of ionic conductivity, lithium transference number, ionic-association degree and self-diffusion coefficient. Accordingly, the electrolyte is employed in a lithium battery using lithium iron phosphate as the selected cathode. The battery delivers a stable capacity of 150 mAh g-1 and flat working voltage of 3.5 V, thus leading to a theoretical energy density referred to the cathode of 520 Wh kg-1. This battery is considered a suitable energy storage system for advanced applications requiring both high safety and high energy density.

  2. Instability of Ionic Liquid-Based Electrolytes in Li−O2 Batteries

    DEFF Research Database (Denmark)

    Das, Supti; Højberg, Jonathan; Knudsen, Kristian Bastholm;

    2015-01-01

    Ionic liquids (ILs) have been proposed as promising solvents for Li−air battery electrolytes. Here, several ILs have been investigated using differential electrochemical mass spectrometry (DEMS) to investigate the electrochemical stability in a Li−O2 system, by means of quantitative determination...

  3. Conductivity and electrical studies of plasticized carboxymethyl cellulose based proton conducting solid biopolymer electrolytes

    Science.gov (United States)

    Isa, M. I. N.; Noor, N. A. M.

    2015-12-01

    In this paper, a proton conducting solid biopolymer electrolytes (SBE) comprises of carboxymethyl cellulose (CMC) as polymer host, ammonium thiocyanate (NH4SCN) as doping salt and ethylene carbonate (EC) as plasticizer has been prepared via solution casting technique. Electrical Impedance Spectroscopy (EIS) was carried out to study the conductivity and electrical properties of plasticized CMC-NH4SCN SBE system over a wide range of frequency between 50 Hz and 1 MHz at temperature range of 303 to 353 K. Upon addition of plasticizer into CMC-NH4SCN SBE system, the conductivity increased from 10-5 to 10-2 Scm-1. The highest conductivity was obtained by the electrolyte containing 10 wt.% of EC. The conductivity of plasticized CMC-NH4SCN SBE system by various temperatures obeyed Arrhenius law where the ionic conductivity increased as the temperature increased. The activation energy, Ea was found to decrease with enhancement of EC concentration. Dielectric studies for the highest conductivity electrolyte obeyed non-Debye behavior. The conduction mechanism for the highest conductivity electrolyte was determined by employing Jonsher's universal power law and thus, can be represented by the quantum mechanical tunneling (QMT) model.

  4. Dye-sensitised photoelectrochemical solar cells with polyacrylonitrile based solid polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Ileperuma, O.A.; Somasundaram, S. [University of Peradeniya (Sri Lanka). Dept. of Chemistry; Dissanayake, M.A.K.L. [University of Peradeniya (Sri Lanka). Dept. of Physics

    2002-07-05

    Novel all solid state dye-sensitised photoelectrochemical solar cells of the type, FTO-TiO{sub 2}-dye-PAN, EC, PC, Pr{sub 4}N{sup +}I{sup -}, I{sub 2}-Pt-FTO, have been fabricated and characterised using current-voltage characteristics and action spectra. Liquid electrolyte generally used for such solar cells has been successfully replaced by a quasi solid electrolyte comprised of polyacrylonitrile (PAN) with ethylene carbonate (EC) and propylene carbonate (PC) as plasticisers and Pr{sub 4}N{sup +}I{sup -}/I{sub 2} redox couple with tetrapropylammoniumiodide as the complexing salt. For the polymer electrolyte, the optimum conductivity of 2.95 x 10{sup -3} S cm{sup -1} was obtained for the electrolyte composition, PAN:EC:PC=15:35:50 (wt.%). The short circuit current density (J{sub SC}) and the open circuit voltage (V{sub OC}) obtained for an incident light intensity of 600 W m{sup -2} were 3.73 mA cm{sup -2} and 0.69 V, respectively. This corresponds to an overall quantum efficiency of 2.99%. From the action spectrum, the maximum incident photon conversion efficiency (IPCE) of 33% was obtained for incident light of wavelength 480 nm.(author)

  5. Characterization of plasticized PMMA–LiBF4 based solid polymer electrolytes

    Indian Academy of Sciences (India)

    S Rajendran; T Uma

    2000-02-01

    Polymer electrolyte films prepared from poly(methyl methacrylate) and LiBF4 with different concentrations of plasticizer (DBP) are described. The formation of polymer–salt complex has been confirmed by FTIR spectral studies. The temperature dependence of conductivity of polymer films seems to obey the VTF relation. Values of conductivities of the polymer complexes are presented and discussed.

  6. PREPARATION AND CHARACTERIZATION OF PVA BASED SOLID POLYMER ELECTROLYTES FOR ELECTROCHEMICAL CELL APPLICATIONS

    Institute of Scientific and Technical Information of China (English)

    Anji Reddy Polu; Ranveer Kumar

    2013-01-01

    Solid polymer electrolyte films containing poly(vinyl alcohol) (PVA) and magnesium nitrate (Mg(NO3)2) were prepared by solution casting technique and characterized by using XRD,FT1R,DSC and AC impedance spectroscopic analysis.The amorphous nature of the polymer electrolyte films has been confirmed by XRD.The complex formation between PVA and Mg salt has been confirmed by FTIR.The glass transition temperature decreases with increasing the Mg salt concentration.The AC impedance studies are performed to evaluate the ionic conductivity of the polymer electrolyte films in the range of 303-383 K,and the temperature dependence seems to obey the Arrhenius behavior.Transport number measurements show that the charge transport is mainly due to ions.Electrochemical cell of configuration Mg/(PVA + Mg(NO3)2) (70:30)/(I2 + C + electrolyte) has been fabricated.The discharge characteristics of the cell were studied for a constant load of 100 kΩ.

  7. Improving cyclic stability of lithium cobalt oxide based lithium ion battery at high voltage by using trimethylboroxine as an electrolyte additive

    International Nuclear Information System (INIS)

    Highlights: •TMB is effective as electrolyte additive for improving cyclic stability of high voltage LiCoO2/graphite battery. •TMB is oxidized preferentially to electrolyte, forming a compact and thin protective film on LiCoO2. •This film protects LiCoO2 from destruction and suppresses electrolyte decomposition. -- Abstract: Trimethylboroxine (TMB) is used as electrolyte additive to improve the cyclic stability of LiCoO2/graphite full cell under high voltage. It is found that capacity retention of LiCoO2/graphite cell at 0.3C rate after 200 cycles between 3.0 ∼ 4.5 V is improved from 29 % to 66 % by applying 0.5 % (by weight) TMB in EC-based electrolyte. Charge-discharge tests on graphite/Li and LiCoO2/Li half cells demonstrate that the improvement in cyclic stability of the full cell results from the contribution of TMB to the enforced stability of LiCoO2 cathode. Cyclic voltammogram shows that TMB is oxidized preferentially to the EC-based electrolyte, while physical characterizations, from SEM, TEM, FTIR and XPS, indicate that TMB helps build a thin but protective film on LiCoO2, which improves the interfacial stability of high voltage electrode/electrolyte

  8. Highly porous lithium-ion conducting solvent-free poly(vinylidene fluoride-co-hexafluoropropylene)/poly(ethyl methacrylate) based polymer blend electrolytes for Li battery applications

    International Nuclear Information System (INIS)

    Plasticised polymer blend electrolytes based on poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-co-HFP) and poly(ethyl methacrylate) (PEMA) were prepared for different lithium salts LiX (X = ClO4, CF3SO3, BF4 and N[CF3SO2]2) using facile solution casting. To confirm the structures and complexations of the electrolyte films, the prepared electrolytes were subjected to XRD and FTIR analysis. TG–DTA was used to ascertain the thermal stability of the electrolytes, and the porous nature of the electrolytes was identified using scanning electron microscopy via ion-hopping conduction. AC impedance analysis was performed for all the electrolyte samples at various temperatures from 303 to 363 K. The results suggest that among the various lithium salts, LiN[CF3SO2]2-based electrolytes exhibited the highest ionic conductivity (0.918 × 10−3 S cm−1). The temperature dependence of the ionic conductivity also complies with the VTF relation

  9. Optimizing the Manufacturing Method of Half-Cell Fuel Cell Based on Solid Electrolyte with Hydrogen Ion Conductivity

    Directory of Open Access Journals (Sweden)

    Naghmeh Mirab

    2012-01-01

    Full Text Available Barium cerate-based perovskite oxides are protonic conductor candidates for intermediate temperature solid oxide fuel cells due to their high ionic conductivity and good sinterability. The aim of the present study is to fabricate a half-cell single-cell includes substrate, anode and electrolyte layers. The exact composition of BaZr0.1Ce0.7Y0.2O3─δ (BZCY7 has been selected as a proton conducting electrolyte. The fabrication process of a dense electrolyte membrane on a NiO- BaZr0.1Ce0.7Y0.2O3─δ (NiO-BZCY7 anode substrate has been studied by a co-pressing process after co-firing at 1400ºC. BZCY7 powders were synthesized by solid-state reaction method after calcinations at 1150ºC. A single phase was obtained at this low temperature. The phase composition of the resulting specimens was investigated using X-ray diffraction (XRD analysis. Scanning electron microscope (SEM was used to evaluate the features of the synthesized powders and also the condition of connected layers in half-cell.

  10. Ionic liquids and oligomer electrolytes based on the B(CN)4(-) anion; ion association, physical and electrochemical properties.

    Science.gov (United States)

    Scheers, Johan; Pitawala, Jagath; Thebault, Frederic; Kim, Jae-Kwang; Ahn, Jou-Hyeon; Matic, Aleksandar; Johansson, Patrik; Jacobsson, Per

    2011-09-01

    The role of B(CN)(4)(-) (Bison) as a component of battery electrolytes is addressed by investigating the ionic conductivity and phase behaviour of ionic liquids (ILs), ion association mechanisms, and the electrochemical stability and cycling properties of LiBison based electrochemical cells. For C(4)mpyrBison and C(2)mimBison ILs, and mixtures thereof, high ionic conductivities (3.4 ≤σ(ion)≤ 18 mS cm(-1)) are measured, which together with the glass transition temperatures (-80 ≤T(g)≤-76 °C) are found to shift systematically for most compositions. Unfortunately, poor solubility of LiBison in these ILs hinders their use as solvents for lithium salts, although good NaBison solubility offers an alternative application in Na(+) conducting electrolytes. The poor IL solubility of LiBison is predicted to be a result of a preferred monodentate ion association, according to first principles modelling, supported by Raman spectroscopy. The solubility is much improved in strongly Li(+) coordinating oligomers, for example polyethylene glycol dimethyl ether (PEGDME), with the practical performance tested in electrochemical cells. The electrolyte is found to be stable in Li/LiFePO(4) coin cells up to 4 V vs. Li and shows promising cycling performance, with a capacity retention of 99% over 22 cycles. PMID:21776511

  11. Dynamics and relaxation of charge carriers in poly(methylmethacrylate)-lithium salt based polymer electrolytes plasticized with ethylene carbonate

    Science.gov (United States)

    Pal, P.; Ghosh, A.

    2016-07-01

    In this paper, we have studied the dynamics and relaxation of charge carriers in poly(methylmethacrylate)-lithium salt based polymer electrolytes plasticized with ethylene carbonate. Structural and thermal properties have been examined using X-ray diffraction and differential scanning calorimetry, respectively. We have analyzed the complex conductivity spectra by using power law model coupled with the contribution of electrode polarization at low frequencies and high temperatures. The temperature dependence of the ionic conductivity and crossover frequency exhibits Vogel-Tammann-Fulcher type behavior indicating a strong coupling between the ionic and the polymer chain segmental motions. The scaling of the ac conductivity indicates that relaxation dynamics of charge carriers follows a common mechanism for all temperatures and ethylene carbonate concentrations. The analysis of the ac conductivity also shows the existence of a nearly constant loss in these polymer electrolytes at low temperatures and high frequencies. The fraction of free anions and ion pairs in polymer electrolyte have been obtained from the analysis of Fourier transform infrared spectra. It is observed that these quantities influence the behavior of the composition dependence of the ionic conductivity.

  12. Synthesis and studies of boron based anion receptors and their use in non-aqueous electrolytes for lithium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Sun, X.; Yang, X.Q.; Lee, H.S.; McBreen, J. [Brookhaven National Lab., Upton, NY (United States); Choi, L.S. [Naval Research Lab., Washington, DC (United States)

    1998-12-31

    A new family of anion receptors based on boron compounds has been synthesized. These compounds can be used as anion receptors in lithium battery electrolytes and can greatly increase solubility and ionic conductivities of various lithium salts, such as LiF, LiCl, CF{sub 3}COOLi and C{sub 2}F{sub 5}COOLi, in DME solutions. Near Edge X-ray Absorption Fine Structure (NEXAFS) spectroscopy studies show that Cl{sup {minus}} anions of LiCl are complexed with these compounds in DME solutions. The electrochemical stability of lithium salts and one of the boron compounds in deferent solvents was studied. For the first time, LiF has been successfully used as conducting salt in a novel electrolyte with this boron compound as an additive in DME. A rechargeable Li/LiMn{sub 2}O{sub 4} cell using this electrolyte was successfully cycled 51 times. However, the capacity fades with cycling due to decomposition of the solvent. The cycling performance of the battery was greatly improved by replacing DME with PC-EC-DMC as the solvent.

  13. Synthesis, dynamic properties and electrochemical stability of organic-inorganic hybrid polymer electrolytes with double core branched structures based on polyether, cyanuric chloride and alkoxysilane

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • New cyanuric chloride based double-core solid hybrid electrolyte is synthesized. • Conductivity of the hybrid electrolyte follows Vogel-Tamman-Fulcher behavior. • Hybrid electrolyte possesses maximum ionic conductivity of 9.5 × 10−5 Scm−1 at 30 °C. • PGSE NMR reveals ion pairs and segmental mobility affect Li diffusion coefficient. • Two local environments are identified for Li+ ions in the hybrid electrolyte. - Abstract: A new organic-inorganic solid hybrid electrolyte based on 2,4,6-trichloro-1,3,5-triazine, triblock co-polymer poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) bis(2-aminopropyl ether), poly(ethylene glycol) diglycidyl ether, and 3-(glycidyloxypropyl)trimethoxysilane doped with LiClO4 salt is synthesized by a sol-gel process. Fourier transform infrared spectroscopy and 13C NMR results reveal the successful synthesis of the organic-inorganic hybrid electrolyte. The conductivity of the hybrid electrolyte follows a VTF (Vogel-Tamman-Fulcher)-like behavior, implying that the diffusion of charge carriers is assisted by the segmental motions of polymer chains. The Li-ion mobility is determined from 7Li static NMR linewidth and diffusion coefficient measurements; both are correlated with their ionic conductivities. The maximum ionic conductivity of 9.5 × 10−5 S cm−1 at 30 °C is obtained for the hybrid electrolyte with the [O]/[Li] ratio of 32. The electrochemical stability window of 4 V ensures the hybrid electrolyte as a potential candidate for low voltage lithium ion batteries

  14. Comparative Studies of the Electrochemical and Thermal Stability of Composite Electrolytes for Lithium Battery Using Two Types of Boron-Based Anion Receptors

    Energy Technology Data Exchange (ETDEWEB)

    Yang, X. Q.; Lee, H. S.; Sun, X.; McBreen, J.

    1999-10-17

    Comparative studies were done on two new types of boron based anion receptors, tris(pentafluorophenyl) borane (TFPB) and tris(pentafluorophenyl) borate (TFPBO), regarding conductivity enhancement electrochemical and thermal stability when used as additives in composite electrolytes for lithium batteries. Both additives enhance the ionic conductivity of electrolytes of simple lithium salts, LiF, CF{sub 3}CO{sub 2}Li and C{sub 2}F{sub 5}CO{sub 2}Li in several organic solvents. The electrochemical windows of TPFB based electrolytes in ethylene carbonate (EC)-propylene carbonate (PC)-dmethyl carbonate (DMC) (1:1:3, v/v) are up to 5, 4.76 and 4.96 V for LiF, CF{sub 3}CO{sub 2}Li and C{sub 2}F{sub 5}CO{sub 2}Li respectively. TPFBO has lower electrochemical stability compared to TPFB. The thermal stability of pure TFPB is better than TFPBO. The lithium salt complexes have higher thermal stability than these two compounds. TPFB based electrolytes showed high cycling efficiencies and good cycleability when they were tested in Li/LiMn{sub 2}O{sub 4} cells. The capacity retention of the cells using TFPB based electrolytes during multiple cycling is better than those using TFPBO based electrolytes.

  15. Preparation of low-platinum-content platinum-nickel, platinum-cobalt binary alloy and platinum-nickel-cobalt ternary alloy catalysts for oxygen reduction reaction in polymer electrolyte fuel cells

    Science.gov (United States)

    Li, Mu; Lei, Yanhua; Sheng, Nan; Ohtsuka, Toshiaki

    2015-10-01

    A series of low-platinum-content platinum-nickel (Pt-Ni), platinum-cobalt (Pt-Co) binary alloys and platinum-nickel-cobalt (Pt-Ni-Co) ternary alloys electrocatalysts were successfully prepared by a three-step process based on electrodeposition technique and studied as electrocatalysts for oxygen reduction reaction (ORR) in polymer-electrolyte fuel cells. Kinetics of ORR was studied in 0.5 M H2SO4 solution on the Pt-Ni, Pt-Co and Pt-Ni-Co alloys catalysts using rotating disk electrode technique. Both the series of Pt-Ni, Pt-Co binary alloys and the Pt-Ni-Co ternary alloys catalysts exhibited an obvious enhancement of ORR activity in comparison with pure Pt. The significant promotion of ORR activities of Pt-Ni and Pt-Co binary alloys was attributed to the enhancement of the first electron-transfer step, whereas, Pt-Ni-Co ternary alloys presented a more complicated mechanism during the electrocatalysis process but a much more efficient ORR activities than the binary alloys.

  16. Characterization of CH3SO3H-doped PMMA/PVP blend-based proton-conducting polymer electrolytes and its application in primary battery

    Science.gov (United States)

    Ambika, C.; Hirankumar, G.

    2016-02-01

    Various compositions of solid blend polymer electrolytes based on poly(methyl methacrylate) (PMMA)/poly(vinyl pyrrolidone) (PVP) complexed with methanesulfonic acid (MSA) as proton donor were prepared by solution casting technique. The complex nature of polymer blend with MSA was confirmed by Fourier transform infrared spectroscopy. Good thermal stability of PMMA/PVP blend polymer electrolyte was identified by thermogravimetric analysis. The surface morphology of the prepared electrolytes was studied through optical microscopy. Ion transport number was determined in the range of 0.93-0.97 for proton-conducting blend polymer electrolytes. The maximum conductivity value was calculated as 2.51 × 10-5 S/cm at 303 K for 14.04 mol% MSA-doped polymer electrolytes. Dielectric studies were also carried out. The electrochemical stability window of blend polymer electrolyte was found to be 1.82 V. Primary proton battery was fabricated with Zn + ZnSO4·7H2O/solid polymer electrolytes/MnO2. The discharge characteristics were studied at constant current drain of 5, 20 and 50 μA. The energy and power density were calculated as 0.27 W h kg-1 and 269.23 mW kg-1 for 20 μA of discharge, respectively.

  17. Towards A Model-Based Prognostics Methodology For Electrolytic Capacitors: A Case Study Based On Electrical Overstress Accelerated Aging

    Data.gov (United States)

    National Aeronautics and Space Administration — This paper presents a model-driven methodology for predict- ing the remaining useful life of electrolytic capacitors. This methodology adopts a Kalman filter...

  18. A Model-based Prognostics Methodology for Electrolytic Capacitors Based on Electrical Overstress Accelerated Aging

    Data.gov (United States)

    National Aeronautics and Space Administration — A remaining useful life prediction methodology for elec- trolytic capacitors is presented. This methodology is based on the Kalman filter framework and an empirical...

  19. Investigation of Ionic Conductivity of - MgCl2 Based Solid Polymer Electrolyte

    Science.gov (United States)

    Sundar, M.; Poovizhi, P. N.; Arunkarthikeyan, J.; Selladurai, S.

    2006-06-01

    Novel solid polymeric electrolyte (SPE) consisting of Poly (ethylene oxide) PEO with magnesium chloride as the electrolyte salt has been prepared by solution casting technique. Measurements with differential scanning calorimetry (DSC) indicates the modification of PEO crystalline structure with increasing content of magnesium salt up to 20 wt% and increase in crystallinity at higher concentration. FTIR studies indicates the interaction of Mg cations with ether oxygen of PEO, Ionic conductivity increases with increase in salt content, and it is optimized at 20 wt% Mg salt. The decrease in ionic conductivity at higher salt content above 20 wt% is due to ion-ion interaction, which leads to ion pair formation and increase in relative crystallanity fraction due to recrystallization above 15wt%.

  20. Lithium-Ion Electrolytes Containing Phosphorous-Based, Flame-Retardant Additives

    Science.gov (United States)

    Smart, Marshall C.; Smith, Kiah A.; Bugga, Ratnakumar V.; Prakash, G. K. Surya

    2010-01-01

    Future NASA missions aimed at exploring Mars, the Moon, and the outer planets require rechargeable batteries that can operate over a wide temperature range (-60 to +60 C) to satisfy the requirements of various applications. In addition, many of these applications will require improved safety, due to their use by humans. Currently, the state-of-the-art lithium-ion (Li-ion) system has been demonstrated to operate over a wide range of temperatures (-40 to +40 C); however, abuse conditions can often lead to cell rupture and fire. The nature of the electrolyte can greatly affect the propensity of the cell/battery to catch fire, given the flammability of the organic solvents used within. Li-ion electrolytes have been developed that contain a flame-retardant additive in conjunction with fluorinated co-solvents to provide a safe system with a wide operating temperature range. Previous work incorporated fluorinated esters into multi-component electrolyte formulations, which were demonstrated to cover a temperature range from 60 to +60 C. This work was described in Fluoroester Co-Solvents for Low-Temperature Li+ Cells (NPO-44626), NASA Tech Briefs, Vol. 33, No. 9 (September 2009), p. 37; and Optimized Li-Ion Electrolytes Con tain ing Fluorinated Ester Co-Solvents (NPO-45824), NASA Tech Briefs, Vol. 34, No. 3 (March 2010), p. 48. Other previous work improved the safety characteristics of the electrolytes by adding flame-retardant additives such as triphenyl phosphate (TPhPh), tri-butyl phosphate (TBuPh), triethyl phosphate (TEtPh), and bis(2,2,2-trifluoroethyl) methyl phosphonate (TFMPo). The current work involves further investigation of other types of flame-retardant additives, including tris(2,2,2-trifluoroethyl) phosphate, tris(2,2,2-trifluoroethyl) phosphite, triphenylphosphite, diethyl ethylphosphonate, and diethyl phenylphosphonate added to an electrolyte composition intended for wide operating temperatures. In general, many of the formulations investigated in this

  1. An Aqueous Redox Flow Battery Based on Neutral Alkali Metal Ferri/ferrocyanide and Polysulfide Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Wei, Xiaoliang; Xia, Gordon; Kirby, Brent W.; Thomsen, Edwin C.; Li, Bin; Nie, Zimin; Graff, Gordon L.; Liu, Jun; Sprenkle, Vincent L.; Wang, Wei

    2015-11-13

    Aiming to explore low-cost redox flow battery systems, a novel iron-polysulfide (Fe/S) flow battery has been demonstrated in a laboratory cell. This system employs alkali metal ferri/ferrocyanide and alkali metal polysulfides as the redox electrolytes. When proper electrodes, such as pretreated graphite felts, are used, 78% energy efficiency and 99% columbic efficiency are achieved. The remarkable advantages of this system over current state-of-the-art redox flow batteries include: 1) less corrosive and relatively environmentally benign redox solutions used; 2) excellent energy and utilization efficiencies; 3) low cost for redox electrolytes and cell components. These attributes can lead to significantly reduced capital cost and make the Fe/S flow battery system a promising low-cost energy storage technology. The major drawbacks of the present cell design are relatively low power density and possible sulfur species crossover. Further work is underway to address these concerns.

  2. Sodium-ion electrolytes based on ionic liquids: a role of cation-anion hydrogen bonding.

    Science.gov (United States)

    Chaban, Vitaly V; Andreeva, Nadezhda A

    2016-08-01

    Recent success of the sodium-ion batteries fosters an academic interest for their investigation. Room-temperature ionic liquids (RTILs) constitute universal solvents providing non-volatility and non-flammability to electrolytes. In the present work, we consider four families of RTILs as prospective solvents for NaBF4 and NaNO3 with an inorganic salt concentration of 25 and 50 mol%. We propose a methodology to rate RTILs according to their solvation capability using parameters of the computed radial distribution functions. Hydrogen bonds between the cations and the anions of RTILs were found to indirectly favor sodium solvation, irrespective of the particular RTIL and its concentration. The best performance was recorded in the case of cholinium nitrate. The reported observations and correlations of ionic structures and properties offer important assistance to an emerging field of sodium-ion batteries. Graphical Abstract Sodium-ion electrolytes. PMID:27381471

  3. Efficiency enhancement in dye sensitized solar cells using gel polymer electrolytes based on a tetrahexylammonium iodide and MgI2 binary iodide system.

    Science.gov (United States)

    Bandara, T M W J; Dissanayake, M A K L; Jayasundara, W J M J S R; Albinsson, I; Mellander, B-E

    2012-06-28

    Quasi-solid-state dye-sensitized solar cells have drawn the attention of scientists and technologists as a potential candidate to supplement future energy needs. The conduction of iodide ions in quasi-solid-state polymer electrolytes and the performance of dye sensitized solar cells containing such electrolytes can be enhanced by incorporating iodides having appropriate cations. Gel-type electrolytes, based on PAN host polymers and mixture of salts tetrahexylammonium iodide (Hex4N(+)I(-)) and MgI2, were prepared by incorporating ethylene carbonate and propylene carbonate as plasticizers. The salt composition in the binary mixture was varied in order to optimize the performance of solar cells. The electrolyte containing 120% Hex4N(+)I(-) with respect to weight of PAN and without MgI2 showed the highest conductivity out of the compositions studied, 2.5 × 10(-3) S cm(-1) at 25 °C, and a glass transition at -102.4 °C. However, the electrolyte containing 100% Hex4N(+)I(-) and 20% MgI2 showed the best solar cell performance highlighting the influence of the cation on the performance of the cell. The predominantly ionic behaviour of the electrolytes was established from the dc polarization data and all the electrolytes exhibit iodide ion transport. Seven different solar cells were fabricated employing different electrolyte compositions. The best cell using the electrolyte with 100% Hex4N(+)I(-) and 20% MgI2 with respect to PAN weight showed 3.5% energy conversion efficiency and 8.6 mA cm(-2) short circuit current density.

  4. Graphene-based supercapacitors in the parallel-plate electrode configuration: ionic liquids versus organic electrolytes.

    Science.gov (United States)

    Shim, Youngseon; Kim, Hyung J; Jung, Younjoon

    2012-01-01

    Supercapacitors with two single-sheet graphene electrodes in the parallel plate geometry are studied via molecular dynamics (MD) computer simulations. Pure 1-ethyl-3-methylimidazolium tetrafluoroborate (EMI+BF4-) and a 1.1 M solution of EMI+BF4- in acetonitrile are considered as prototypes of room-temperature ionic liquids (RTILs) and organic electrolytes. Electrolyte structure, charge density and associated electric potential are investigated by varying the charges and separation of the two electrodes. Multiple charge layers formed in the electrolytes in the vicinity of the electrodes are found to screen the electrode surface charge almost completely. As a result, the supercapacitors show nearly an ideal electric double layer behavior, i.e., the electric potential exhibits essentially a plateau behavior in the entire electrolyte region except for sharp changes in screening zones very close to the electrodes. Due to its small size and large charge separation, BF4- is considerably more efficient in shielding electrode charges than EMI+. In the case of the acetonitrile solution, acetonitrile also plays an important role by aligning its dipoles near the electrodes; however, the overall screening mainly arises from ions. Because of the disparity of shielding efficiency between cations and anions, the capacitance of the positively-charged anode is significantly larger than that of the negatively-charged cathode. Therefore, the total cell capacitance in the parallel plate configuration is primarily governed by the cathode. Ion conductivity obtained via the Green-Kubo (GK) method is found to be largely independent of the electrode surface charge. Interestingly, EMI+BF4- shows higher GK ion conductivity than the 1.1 M acetonitrile solution between two parallel plate electrodes. PMID:22455024

  5. The Effect of Percutaneous Nephrolithotomy Process on Hemodynamic, Electrolyte and Acid-Base Changes

    Directory of Open Access Journals (Sweden)

    Ercan Baş

    2015-10-01

    Full Text Available Aim: Operation of percutaneous nephrolithotomy (PNL, is the most commonly used method of renal stone surgery. During this operation, kidney must be continually irrigated with isotonic liquid. In our study, we investigated the volume of irrigation, irrigation duration, input the number of percutaneous renal parenchymal thickness and the degree of this finding the effects of on hemodynamic, electrolyte and metabolic changes. Method: 64 patient with an indication for percutaneous nephrolithotomy were included in the study. Before irrigation, during irrigation and the post- irrigation; pulse, systolic and diastolic blood pressure (bp, electrolytes, arterial blood gases were measured. In preoperative and postoperative 1. and 24. hours hemoglobin, creatinine levels were measured. Before the operation; pelvicaliectasis degree, parenchymal thickness, volume and duration of irrigation and the number of percutaneous entry were recorded in all patients. Results: Following the start of irrigation, changes in diastolic and systolic bp and pulse also not statistically significant. No significant change of partial oxygen, carbon dioxide, and oxygen saturation pressure was observed. After the operation, serum sodium, potassium, calcium values are within normal limits, but when compared with preoperative values the decrease of these values statistically significant were observed. Bicarbonate and ph values with irrigation period had a negative correlation. Although not clinically significant parenchymal thickness was found to be negative correlation with decrease of calcium. Additionally degrees of pelvicaliectasis has been found negative correlation with the decrease of sodium and bicarbonate. Conclusion: Hemodynamics and electrolytes did not change significantly both during and after the PNL process, but metabolic acidosis was observed towards the end of the PNL process. In long-term irrigation, repeated percutaneous entrances, people with moderate and severe

  6. Polymer chain organization in tensile-stretched poly(ethylene oxide)-based polymer electrolytes

    Science.gov (United States)

    Burba, Christopher M.; Woods, Lauren; Millar, Sarah Y.; Pallie, Jonathan

    2011-01-01

    Polymer chain orientation in tensile-stretched poly(ethylene oxide)-lithium trifluoromethanesulfonate polymer electrolytes are investigated with polarized infrared spectroscopy as a function of the degree of strain and salt composition (ether oxygen atom to lithium ion ratios of 20:1, 15:1, and 10:1). The 1359 and 1352 cm-1 bands are used to probe the crystalline PEO and P(EO)3LiCF3SO3 domains, respectively, allowing a direct comparison of chain orientation for the two phases. Two-dimensional correlation FT-IR spectroscopy indicates that the two crystalline domains align at the same rate as the polymer electrolytes are stretched. Quantitative measurements of polymer chain orientation obtained through dichroic infrared spectroscopy show that chain orientation predominantly occurs between strain values of 150% and 250%, regardless of salt composition investigated. There are few changes in chain orientation for either phase when the films are further elongated to a strain of 300%; however, the PEO domains are slightly more oriented at the high strain values. The spectroscopic data are consistent with stretching-induced melt-recrystallization of the unoriented crystalline domains in the solution-cast polymer films. Stretching the films pulls polymer chains from the crystalline domains, which subsequently recrystallize with the polymer helices parallel to the stretch direction. If lithium ion conduction in crystalline polymer electrolytes is viewed as consisting of two major components (facile intra-chain lithium ion conduction and slow helix-to-helix inter-grain hopping), then alignment of the polymer helices will affect the ion conduction pathways for these materials by reducing the number of inter-grain hops required to migrate through the polymer electrolyte. PMID:22184475

  7. Polymer chain organization in tensile-stretched poly(ethylene oxide)-based polymer electrolytes.

    Science.gov (United States)

    Burba, Christopher M; Woods, Lauren; Millar, Sarah Y; Pallie, Jonathan

    2011-12-15

    Polymer chain orientation in tensile-stretched poly(ethylene oxide)-lithium trifluoromethanesulfonate polymer electrolytes are investigated with polarized infrared spectroscopy as a function of the degree of strain and salt composition (ether oxygen atom to lithium ion ratios of 20:1, 15:1, and 10:1). The 1359 and 1352 cm(-1) bands are used to probe the crystalline PEO and P(EO)(3)LiCF(3)SO(3) domains, respectively, allowing a direct comparison of chain orientation for the two phases. Two-dimensional correlation FT-IR spectroscopy indicates that the two crystalline domains align at the same rate as the polymer electrolytes are stretched. Quantitative measurements of polymer chain orientation obtained through dichroic infrared spectroscopy show that chain orientation predominantly occurs between strain values of 150% and 250%, regardless of salt composition investigated. There are few changes in chain orientation for either phase when the films are further elongated to a strain of 300%; however, the PEO domains are slightly more oriented at the high strain values. The spectroscopic data are consistent with stretching-induced melt-recrystallization of the unoriented crystalline domains in the solution-cast polymer films. Stretching the films pulls polymer chains from the crystalline domains, which subsequently recrystallize with the polymer helices parallel to the stretch direction. If lithium ion conduction in crystalline polymer electrolytes is viewed as consisting of two major components (facile intra-chain lithium ion conduction and slow helix-to-helix inter-grain hopping), then alignment of the polymer helices will affect the ion conduction pathways for these materials by reducing the number of inter-grain hops required to migrate through the polymer electrolyte.

  8. Nuclear magnetic resonance study of PEO-chitosan based polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Donoso, J.P.; Lopes, L.V.S. [IFSC, Universidade de Sao Paulo, PO Box 369, 13560-970 Sao Carlos-SP (Brazil); Pawlicka, A. [IQSC, Universidade de Sao Paulo, PO Box 780, 13560-970 Sao Carlos-SP (Brazil); Fuentes, S. [Department of Physics, Faculty of Sciences, Universidad Catolica del Norte, Angamos 0610, Antofagasta (Chile); Retuert, P.J. [Department of Material Sciences, Faculty of Mathematical and Physical Sciences, Universidad de Chile, Tupper 2069, Santiago (Chile); Gonzalez, G. [Department of Chemistry, Faculty of Sciences, Universidad de Chile, Casilla 653, Santiago (Chile)

    2007-12-31

    This work investigates lithium dynamics in a series of polymer electrolytes formed by poly(ethylene oxide) PEO, chitosan (QO), amino propil siloxane (pAPS) and lithium perchlorate by means of nuclear magnetic resonance techniques. Lithium ({sup 7}Li) lineshapes and spin-lattice relaxation times were measured as a function of temperature. The results suggest that the chemical functionality of QO, particularly the amine group, participate in coordinating lithium ion in the composites. The competition between QO and PEO for lithium ions is evident in the binary system. In the ternary electrolyte containing PEO, QO and pAPS, it is observed that the lithium ions can competitively interact with the two polymers. The heterogeneity, at a local microscopic scale, is revealed by a temperature-dependent equilibrium of lithium ion concentration between at least two different microphases; on 37dominated by the interactions with chitosan and the other one with polyether. The data of the ternary electrolyte was analysed by assuming two lithium dynamics, the first one associated to the motion of the lithium ion dissolved in PEO and the second one associated to those complexed by the chitosan. (author)

  9. Development and Characterization of Poly(1-vinylpyrrolidone-co-vinyl acetate Copolymer Based Polymer Electrolytes

    Directory of Open Access Journals (Sweden)

    Nurul Nadiah Sa’adun

    2014-01-01

    Full Text Available Gel polymer electrolytes (GPEs are developed using poly(1-vinylpyrrolidone-co-vinyl acetate [P(VP-co-VAc] as the host polymer, lithium bis(trifluoromethane sulfonimide [LiTFSI] as the lithium salt and ionic liquid, and 1-ethyl-3-methylimidazolium bis(trifluoromethylsulfonyl imide [EMImTFSI] by using solution casting technique. The effect of ionic liquid on ionic conductivity is studied and the optimum ionic conductivity at room temperature is found to be 2.14 × 10−6 S cm−1 for sample containing 25 wt% of EMImTFSI. The temperature dependence of ionic conductivity from 303 K to 353 K exhibits Arrhenius plot behaviour. The thermal stability of the polymer electrolyte system is studied by using thermogravimetric analysis (TGA while the structural and morphological properties of the polymer electrolyte is studied by using Fourier transform infrared (FTIR spectroscopy and X-ray diffraction analysis (XRD, respectively.

  10. Effect of aqueous electrolytes on the electrochemical behaviors of supercapacitors based on hierarchically porous carbons

    Science.gov (United States)

    Zhang, Xiaoyan; Wang, Xianyou; Jiang, Lanlan; Wu, Hao; Wu, Chun; Su, Jingcang

    2012-10-01

    Hierarchically porous carbons (HPCs) have been prepared by sol-gel self-assembly technology with nickel oxide and surfactant as the dual template. The porous carbons are further activated by nitric acid. The electrochemical behaviors of supercapacitors using HPCs as electrode material in different aqueous electrolytes, e.g., (NH4)2SO4, Na2SO4, H2SO4 and KOH are studied by cyclic voltametry, galvanostatic charge/discharge, cyclic life, leakage current, self-discharge and electrochemical impedance spectroscopy. The results demonstrate that the supercapacitors in various electrolytes perform definitely capacitive behaviors; especially in 6 M KOH electrolyte the supercapacitor represents the best electrochemical performance, the shortest relaxation time, and nearly ideal polarisability. The energy density of 8.42 Wh kg-1 and power density of 17.22 kW kg-1 are obtained at the operated voltage window of 1.0 V. Especially, the energy density of 11.54 Wh kg-1 and power density of 10.58 kW kg-1 can be achieved when the voltage is up to 1.2 V.

  11. Conducting polymer actuator based on chemically deposited polypyrrole and polyurethane-based solid polymer electrolyte working in air

    International Nuclear Information System (INIS)

    Conducting polymers (CPs), such as polypyrrole, polythiophene, and polyaniline, are unique in that they have switchable properties due to their two or more mechanically stable oxidation states. Thus, their films or coatings can be easily switched by the application of a small voltage and current to change their volume during electrochemical redox processes. In particular, polypyrrole (PPy) has been studied most extensively because of its high electrical conductivity and good environmental stability under ambient conditions. In this work, we have studied a new CP actuator, fully polymeric, assembled with two PPy film electrodes and a solid polymer electrolyte (SPE), polyurethane/Mg(ClO4)2. Polyurethanes (PUs) were synthesized from 4,4'-diphenylmethane diisocyanate (MDI), 1,4-butanediol (1,4-BD) and three types of polyol: poly(ethylene glycol) (PEG), poly(propylene glycol) (PPG), and PPG-block-PEG-block-PPG (PPG-co-PEG). The chemical polymerization of PPy by immersion in Py monomer aqueous solution and oxidant aqueous solution is an adequate method to prepare PU/PPy composite film as an actuator. To find the proper thickness of the PPy coating layer for actuation, we measured the displacements of the actuators according to the thickness of the PPy coating layer. The displacement of all actuators is discussed in connection with the properties of the SPE and PPy. All the results obtained in this work show the feasibility of electrochemomechanical devices based on PPy and SPE film being able to work in air

  12. Low molecular mass organogelator based gel electrolyte with effective charge transport property for long-term stable quasi-solid-state dye-sensitized solar cells.

    Science.gov (United States)

    Huo, Zhipeng; Dai, Songyuan; Zhang, Changneng; Kong, Fantai; Fang, Xiaqin; Guo, Lei; Liu, Weiqing; Hu, Linhua; Pan, Xu; Wang, Kongjia

    2008-10-16

    Stable quasi-solid-state dye-sensitized solar cells (DSC) were fabricated using 12-hydroxystearic acid as a low molecular mass organogelator (LMOG) to form gel electrolyte. TEM image of the gel exhibited the self-assembled network constructed by the LMOG, which hindered flow and volatilization of the liquid. The formation of less-mobile polyiodide ions such as I 3 (-) and I 5 (-) confirmed by Raman spectroscopy increased the conductivity of the gel electrolytes by electronic conduction process, which should be rationalized by the Grotthuss-type electron exchange mechanism caused by rather packed polyiodide species in the electrolytes. The results of the accelerated aging tests showed that the gel electrolyte based dye-sensitized solar cell could retain over 97% of its initial photoelectric conversion efficiency value after successive heating at 60 degrees C for 1000 h and device degradation was also negligible after one sun light soaking with UV cutoff filter for 1000 h.

  13. Organic electrolytes for sodium batteries

    Science.gov (United States)

    Vestergaard, B.

    1992-09-01

    A summary of earlier given status reports in connection with the project on organic electrolytes for sodium batteries is presented. The aim of the investigations was to develop new room temperature molten salts electrolytes mainly with radical substituted heterocyclic organic chlorides mixed with aluminum chloride. The new electrolytes should have an ionic conductivity comparable with MEIC1:AlCl3 or better. A computer model program MOPAC (Molecular Orbital Package) was to be included to calculate theoretically reduction potentials for a variety of organic cations. Furthermore, MOPAC could be utilized to predict the electron densities, and then give a prediction of the stability of the organic cation.

  14. Synthesis and characterization of castor oil-based polyurethane for potential application as host in polymer electrolytes

    Indian Academy of Sciences (India)

    S Ibrahim; A Ahmad; N S Mohamed

    2015-09-01

    Polyurethane (PU) based on polyol, derived from castor oil has been synthesized and characterized for potential use as a base material for electrolytes. Transesterification process of castor oil formed a polyol with hydroxyl value of 190 mg KOH g–1 and molecular weight of 2786 g mol–1. The polyols together with 4,4′-diphenylmethane diisocyanate were used to synthesize the desired bio-based PU. The molecular structure of PU was investigated by Fourier transform infrared (FTIR) spectroscopy. The disappearance of NCO peak in the FTIR spectrum at 2270–2250 cm–1 showed that diisocyanate has completely reacted to form PU. Morphological characteristic of the PU film was analysed using scanning electron microscopy, whereas thermal characteristics of the materials were characterized using dynamic mechanical analysis and thermal gravimetric analysis. The cross-sectional micrograph showed that the prepared film was highly amorphous and homogeneous. Thermal studies revealed that the film had low glass transition temperature, –15.8°C, and was thermally stable up to 259°C. These observations indicated the synthesized PU possessed favourable properties to act as a base material in polymer electrolytes.

  15. An ether-functionalised cyclic sulfonium based ionic liquid as an electrolyte for electrochemical double layer capacitors

    Science.gov (United States)

    Neale, Alex R.; Murphy, Sinead; Goodrich, Peter; Schütter, Christoph; Hardacre, Christopher; Passerini, Stefano; Balducci, Andrea; Jacquemin, Johan

    2016-09-01

    A novel cyclic sulfonium cation-based ionic liquid (IL) with an ether-group appendage and the bis{(trifluoromethyl)sulfonyl}imide anion was synthesised and developed for electrochemical double layer capacitor (EDLC) testing. The synthesis and chemical-physical characterisation of the ether-group containing IL is reported in parallel with a similarly sized alkyl-functionalised sulfonium IL. Results of the chemical-physical measurements demonstrate how important transport properties, i.e. viscosity and conductivity, can be promoted through the introduction of the ether-functionality without impeding thermal, chemical or electrochemical stability of the IL. Although the apparent transport properties are improved relative to the alkyl-functionalised analogue, the ether-functionalised sulfonium cation-based IL exhibits moderately high viscosity, and poorer conductivity, when compared to traditional EDLC electrolytes based on organic solvents (propylene carbonate and acetonitrile). Electrochemical testing of the ether-functionalised sulfonium IL was conducted using activated carbon composite electrodes to inspect the performance of the IL as a solvent-free electrolyte for EDLC application. Good cycling stability was achieved over the studied range and the performance was comparable to other solvent-free, IL-based EDLC systems. Nevertheless, limitations of the attainable performance are primarily the result of sluggish transport properties and a restricted operative voltage of the IL, thus highlighting key aspects of this field which require further attention.

  16. A Multi-Point Sensor Based on Optical Fiber for the Measurement of Electrolyte Density in Lead-Acid Batteries

    Science.gov (United States)

    Cao-Paz, Ana M.; Marcos-Acevedo, Jorge; del Río-Vázquez, Alfredo; Martínez-Peñalver, Carlos; Lago-Ferreiro, Alfonso; Nogueiras-Meléndez, Andrés A.; Doval-Gandoy, Jesús

    2010-01-01

    This article describes a multi-point optical fiber-based sensor for the measurement of electrolyte density in lead-acid batteries. It is known that the battery charging process creates stratification, due to the different densities of sulphuric acid and water. In order to study this process, density measurements should be obtained at different depths. The sensor we describe in this paper, unlike traditional sensors, consists of several measurement points, allowing density measurements at different depths inside the battery. The obtained set of measurements helps in determining the charge (SoC) and state of health (SoH) of the battery. PMID:22319262

  17. A Multi-Point Sensor Based on Optical Fiber for the Measurement of Electrolyte Density in Lead-Acid Batteries

    Directory of Open Access Journals (Sweden)

    Ana M. Cao-Paz

    2010-03-01

    Full Text Available This article describes a multi-point optical fiber-based sensor for the measurement of electrolyte density in lead-acid batteries. It is known that the battery charging process creates stratification, due to the different densities of sulphuric acid and water. In order to study this process, density measurements should be obtained at different depths. The sensor we describe in this paper, unlike traditional sensors, consists of several measurement points, allowing density measurements at different depths inside the battery. The obtained set of measurements helps in determining the charge (SoC and state of health (SoH of the battery.

  18. Quasi-solid-state nanocrystalline TiO2 solar cells using gel network polymer electrolytes based on polysiloxanes

    Institute of Scientific and Technical Information of China (English)

    2003-01-01

    A quasi-solid-state dye-sensitized nanocrystalline porous TiO2 film solar cell was fabricated using a novel gel network polymer electrolyte based on polysiloxanes with both polyethylene oxide internal plasticized side chains and quaternary ammonium groups. The cell exhibited better photoelectrical conversion performance under 60 mW/cm2 irradiation. The short photocurrent (Isc) of 5.0 mA/cm2 and open voltage (Voc) of 0.68 V were achieved, and the energy conversion efficiency (η) and fill factor (ff) were 3.4% and 0.60, respectively.

  19. A microporous gel electrolyte based on poly(vinylidene fluoride-co-hexafluoropropylene)/fully cyanoethylated cellulose derivative blend for lithium-ion battery

    Energy Technology Data Exchange (ETDEWEB)

    Ren Zhong [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China); Liu Yuyan [Department of Applied Chemistry, Harbin Institute of Technology, Harbin 150001 (China)], E-mail: liuyy@hit.edu.cn; Sun Kening; Zhou Xiaoliang; Zhang Naiqing [Science Reseach Center, Harbin Institute of Technology, Harbin 150001 (China)

    2009-02-15

    A gel polymer electrolyte based on the blend of poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) and fully cyanoethylated cellulose derivative (DH-4-CN) was prepared and characterized. Thermal, mechanical, swelling, liquid electrolyte retention and electrochemical properties, as well as microstructures of the prepared polymer electrolytes, were investigated using thermogravimetric analysis, electrochemical impedance spectroscopy, linear sweep voltammetry, and scanning electron microscopy. The results showed that the addition of DH-4-CN could obviously improve the conductivity of PVDF-HFP based electrolyte. The maximum ionic conductivity of 4.36 mS cm{sup -1} at 20 deg. C can be obtained for PVDF-HFP/DH-4-CN 14:1 in the presence of 1 M LiPF{sub 6} in EC and DMC (1:1, w/w). The dry blend membranes exhibit excellent thermal behavior. All the blend electrolytes are electrochemically stable up to about 4.8 V vs. Li/Li{sup +} for all compositions. The results reveal that the composite polymer electrolyte qualifies as a potential application in lithium-ion battery.

  20. Design of an electrolyte composition for stable and rapid charging-discharging of a graphite negative electrode in a bis(fluorosulfonyl)imide-based ionic liquid

    Science.gov (United States)

    Matsui, Yukiko; Yamagata, Masaki; Murakami, Satoshi; Saito, Yasuteru; Higashizaki, Tetsuya; Ishiko, Eriko; Kono, Michiyuki; Ishikawa, Masashi

    2015-04-01

    We evaluate the effects of lithium salt on the charge-discharge performance of a graphite negative electrode in 1-ethyl-3-methylimidazolium bis(fluorosulfonyl)imide (EMImFSI) ionic liquid-based electrolytes. Although the graphite negative electrode exhibits good cyclability and rate capability in both 0.43 mol dm-3 LiFSI/EMImFSI and LiTFSI/EMImFSI (TFSI- = bis(trifluoromethylsulfonyl)imide) at room temperature, only the LiFSI/EMImFSI system enables the graphite electrode to be operated with sufficient discharge capacity at the low temperature of 0 °C, even though there is no noticeable difference in ionic conductivity, compared with LiTFSI/EMImFSI. Furthermore, a clear difference in the low-temperature behaviors of the two cells composed of EMImFSI with a high-concentration of lithium salts is observed. Additionally, charge-discharge operation of the graphite electrode at C-rate of over 5.0 can be achieved using of the high-concentration LiFSI/EMImFSI electrolyte. Considering the low-temperature characteristics in both high-concentration electrolytes, the stable and rapid charge-discharge operation in the high-concentration LiFSI/EMImFSI is presumably attributed to a suitable electrode/electrolyte interface with low resistivity. These results suggest that optimization of the electrolyte composition can realize safe and high-performance lithium-ion batteries that utilize ionic liquid-based electrolytes.

  1. Gel electrolytes based on poly(acrylonitrile)/sulpholane with hybrid TiO2/SiO2 filler for advanced lithium polymer batteries

    International Nuclear Information System (INIS)

    Highlights: • Paper describes properties of gel electrolyte based on PAN with TMS and TiO2-SiO2. • The TiO2-SiO2 oxide composite was precipitated in the emulsion system and used as the fillers. • The capacity of the graphite anode depends on the current rate and the amount of TiO2-SiO2. • For PE3 electrolyte was obtained practical capacity more than 90% of the theoretical capacity. - Abstract: This paper describes the synthesis and properties of a new type of ceramic fillers for composite polymer gel electrolytes. Hybrid TiO2-SiO2 ceramic powders have been obtained by co-precipitation from titanium(IV) sulfate solution using sodium silicate as the precipitating agent. The resulting submicron-size powders have been applied as fillers for composite polymer gel electrolytes for Li-ion batteries based on polyacrylonitrile (PAN) membranes. The powders and gel electrolytes have been examined structurally and electrochemically, showing favorable properties in terms of electrolyte uptake and electrochemical characteristics in Li-ion cells

  2. Enhancement of Oxygen Reduction and Mitigation of Ionomer Dry-Out Using Insoluble Heteropoly Acids in Intermediate Temperature Polymer-Electrolyte Membrane Fuel Cells

    OpenAIRE

    Alessandro Stassi; Irene Gatto; Ada Saccà; Vincenzo Baglio; Aricò, Antonino S.

    2015-01-01

    The use of Cs 0.5 H 0.5 PW 12 O 40 insoluble salt as a superacid promoter in the catalyst layer of a polymer electrolyte membrane fuel cell (PEMFC) has been investigated. An increase of performance has been recorded at intermediate temperatures (110–130 °C) and under low relative humidity (R.H.). The promoter appears to mitigate the ionomer dry-out effects in the catalytic layer and produces an increase of the extent of the catalyst-electrolyte interface as demonstrated by cyclic voltammet...

  3. Conducting polymer-based counter electrode for a quantum-dot-sensitized solar cell (QDSSC) with a polysulfide electrolyte

    International Nuclear Information System (INIS)

    Highlights: ► This is the first report on the use of conducting polymers as counter electrode catalysts for quantum-dot-sensitized solar cells (QDSSCs). ► Conducting polymer materials, i.e., polythiophene (PT), polypyrrole (PPy), and poly(3,4-ethylenedioxythiophene) (PEDOT) were used to prepare counter electrodes for QDSSCs. ► The influences of morphology of the PEDOT-based counter electrode (CE) on the performance of its QDSSC were studied. ► PEDOT electrode exhibits well electrocatalytic activity and stability in the polysulfide electrolyte. ► The efficiency for the QDSSC with PEDOT-CE (1.35%) is comparable to that of the cell with sputtered-Au CE (1.33%). - Abstract: Conducting polymer materials, i.e., polythiophene (PT), polypyrrole (PPy), and poly(3,4-ethylenedioxythiophene) (PEDOT) were used to prepare counter electrodes (CEs) for quantum-dot-sensitized solar cells (QDSSCs). The QDSSC with PEDOT-CE exhibited the highest solar-to-electricity conversion efficiency (η) of 1.35%, which is remarkably higher than those of the cells with PT-CE (0.09%) and PPy-CE (0.41%) and very slightly higher than that of the cell with sputtered-gold-CE (1.33%). Electrochemical impedance spectra (EIS) show that this highest conversion efficiency of the PEDOT-based cell is due to higher electrocatalytic activity and reduced charge transfer resistance at the interface of the CE and the electrolyte, compared to those in the case of the cells with other conducting polymers and bare Au. Furthermore, the influences of morphology of the PEDOT film and the charge passed for its electropolymerization on the performance of its QDSSC were also studied. The higher porosity and surface roughness of the PEDOT matrix, with reference to those of other polymers are understood to be the reason for PEDOT to possess higher electrocatalytic activity at its interface with electrolyte.

  4. 3-V Solid-State Flexible Supercapacitors with Ionic-Liquid-Based Polymer Gel Electrolyte for AC Line Filtering.

    Science.gov (United States)

    Kang, Yu Jin; Yoo, Yongju; Kim, Woong

    2016-06-01

    State-of-the-art solid-state flexible supercapacitors with sufficiently fast response speed for AC line filtering application suffer from limited energy density. One of the main causes of the low energy density is the low cell voltage (1 V), which is limited by aqueous-solution-based gel electrolytes. In this work, we demonstrate for the first time a 3-V flexible supercapacitor for AC line filtering based on an ionic-liquid-based polymer gel electrolyte and carbon nanotube electrode material. The flexible supercapacitor exhibits an areal energy density that is more than 20 times higher than that of the previously demonstrated 1-V flexible supercapacitor (0.66 vs 0.03 μWh/cm(2)) while maintaining excellent capacitive behavior at 120 Hz. The supercapacitor shows a maximum areal power density of 1.5 W/cm(2) and a time constant of 1 ms. The improvement of the cell voltage while maintaining the fast-response capability greatly improves the potential of supercapacitors for high-frequency applications in wearable and/or portable electronics. PMID:27167760

  5. Thin film polymeric gel electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Derzon, Dora K. (1554 Rosalba St. NE., Albuquerque, Bernalillo County, NM 87112); Arnold, Jr., Charles (3436 Tahoe, NE., Albuquerque, Bernalillo County, NM 87111); Delnick, Frank M. (9700 Fleming Rd., Dexter, MI 48130)

    1996-01-01

    Novel hybrid thin film electrolyte, based on an organonitrile solvent system, which are compositionally stable, environmentally safe, can be produced efficiently in large quantity and which, because of their high conductivities .apprxeq.10.sup.-3 .OMEGA..sup.-1 cm.sup.-1 are useful as electrolytes for rechargeable lithium batteries.

  6. Semiconductor Quantum Dot Sensitized Solar Cells Based on Ferricyanide/Ferrocyanide Redox Electrolyte Reaching an Open Circuit Photovoltage of 0.8 V.

    Science.gov (United States)

    Evangelista, Rosemarie M; Makuta, Satoshi; Yonezu, Shota; Andrews, John; Tachibana, Yasuhiro

    2016-06-01

    Semiconductor quantum dot sensitized solar cells (QDSSCs) have rapidly been developed, and their efficiency has recently exceeded 9%. Their performances have mainly been achieved by focusing on improving short circuit photocurrent employing polysulfide electrolytes. However, the increase of open circuit photovoltage (VOC) cannot be expected with QDSSCs based on the polysulfide electrolytes owing to their relatively negative redox potential (around -0.65 V vs Ag/AgCl). Here, we demonstrate enhancement of the open circuit voltage by employing an alternative electrolyte, ferricyanide/ferrocyanide redox couple. The solar cell performance was optimized by investigating the influence of ferricyanide and ferrocyanide concentration on their interfacial charge transfer and transport kinetics. The optimized ferricyanide/ferrocyanide species concentrations (0.01/0.2 M) result in solar energy conversion efficiency of 2% with VOC of 0.8 V. Since the potential difference between the TiO2 conduction band edge at pH 7 and the electrolyte redox potential is about 0.79 V, although the conduction band edge shifts negatively under the negative bias application into the TiO2 electrode, the solar cell with the optimized electrolyte composition has nearly reached the theoretical maximum voltage. This study suggests a promising method to optimize an electrolyte composition for maximizing solar energy conversion efficiency.

  7. Hydroxypropyl Cellulose Based Non-Volatile Gel Polymer Electrolytes for Dye-Sensitized Solar Cell Applications using 1-methyl-3-propylimidazolium iodide ionic liquid

    Science.gov (United States)

    Khanmirzaei, Mohammad Hassan; Ramesh, S.; Ramesh, K.

    2015-12-01

    Gel polymer electrolytes using imidazolium based ionic liquids have attracted much attention in dye-sensitized solar cell applications. Hydroxypropyl cellulose (HPC), sodium iodide (NaI), 1-methyl-3-propylimidazolium iodide (MPII) as ionic liquid (IL), ethylene carbonate (EC) and propylene carbonate (PC) are used for preparation of non-volatile gel polymer electrolyte (GPE) system (HPC:EC:PC:NaI:MPII) for dye-sensitized solar cell (DSSC) applications. The highest ionic conductivity of 7.37 × 10-3 S cm-1 is achieved after introducing 100% of MPII with respect to the weight of HPC. Temperature-dependent ionic conductivity of gel polymer electrolytes is studied in this work. XRD patterns of gel polymer electrolytes are studied to confirm complexation between HPC polymer, NaI and MPII. Thermal behavior of the GPEs is studied using simultaneous thermal analyzer (STA) and differential scanning calorimetry (DSC). DSSCs are fabricated using gel polymer electrolytes and J-V centeracteristics of fabricated dye sensitized solar cells were analyzed. The gel polymer electrolyte with 100 wt.% of MPII ionic liquid shows the best performance and energy conversion efficiency of 5.79%, with short-circuit current density, open-circuit voltage and fill factor of 13.73 mA cm-2, 610 mV and 69.1%, respectively.

  8. Biopolymer electrolytes based on blend of kappa-carrageenan and cellulose derivatives for potential application in dye sensitized solar cell

    International Nuclear Information System (INIS)

    In this work, carboxymethyl kappa-carrageenan was used as the principle host for developing new biopolymer electrolytes based on the blend of carboxymethyl kappa-carrageenan/carboxymethyl cellulose. The blending of carboxymethyl cellulose into carboxymethyl kappa-carragenan was found to be a promising strategy to improve the material properties such as conductive properties. The electrolyte samples were characterized using Fourier transform infrared spectroscopy, scanning electron microscopy, dynamic mechanical analysis, electrochemical impedance spectroscopy, ionic transference number measurement and linear sweep voltammetry in order to investigate their structural, thermal and electrochemical properties. Impedance study showed that the ionic conductivity increased with the increment of ammonium iodide concentration. The highest room temperature ionic conductivity achieved was 2.41 × 10−3 S cm−1 at 30 wt% of the salt. The increment of conductivity was due to the increase of formation of transient cross-linking between the carboxymethyl kappa-carrageenan/carboxymethyl cellulose chains and the doping salt as indicated the Tg trend. The conductivity was also attributed by the increase in the number of charge carriers in the biopolymer electrolytes system. The interactions between polymers and salt were confirmed by FTIR study. The transference number measurements showed that the conductivity was predominantly ionic. Temperature dependent conductivity study showed that conductivity increased with the reciprocal of temperature. The conductivity-temperature plots suggested that the conductivity obeyed the Vogel–Tammann–Fulcher relation and the activation energy for the best conducting sample was 0.010 eV. This system was used for the fabrication of dye sensitized solar cells, FTO/TiO2-dye/CMKC/CMCE-NH4I + I2/Pt. The fabricated cell showed response under light intensity of 100 mW cm−2 with efficiency of 0.13% indicating that the blend biopolymer system has

  9. Poly(Acrylic acid–Based Hybrid Inorganic–Organic Electrolytes Membrane for Electrical Double Layer Capacitors Application

    Directory of Open Access Journals (Sweden)

    Chiam-Wen Liew

    2016-05-01

    Full Text Available Nanocomposite polymer electrolyte membranes (NCPEMs based on poly(acrylic acid(PAA and titania (TiO2 are prepared by a solution casting technique. The ionic conductivity of NCPEMs increases with the weight ratio of TiO2.The highest ionic conductivity of (8.36 ± 0.01 × 10−4 S·cm−1 is obtained with addition of 6 wt % of TiO2 at ambient temperature. The complexation between PAA, LiTFSI and TiO2 is discussed in Attenuated total reflectance-Fourier Transform Infrared (ATR-FTIR studies. Electrical double layer capacitors (EDLCs are fabricated using the filler-free polymer electrolyte or the most conducting NCPEM and carbon-based electrodes. The electrochemical performances of fabricated EDLCs are studied through cyclic voltammetry (CV and galvanostatic charge-discharge studies. EDLC comprising NCPEM shows the specific capacitance of 28.56 F·g−1 (or equivalent to 29.54 mF·cm−2 with excellent electrochemical stability.

  10. Enhancing Specific Energy and Power in Asymmetric Supercapacitors - A Synergetic Strategy based on the Use of Redox Additive Electrolytes

    Science.gov (United States)

    Singh, Arvinder; Chandra, Amreesh

    2016-05-01

    The strategy of using redox additive electrolyte in combination with multiwall carbon nanotubes/metal oxide composites leads to a substantial improvements in the specific energy and power of asymmetric supercapacitors (ASCs). When the pure electrolyte is optimally modified with a redox additive viz., KI, ~105% increase in the specific energy is obtained with good cyclic stability over 3,000 charge-discharge cycles and ~14.7% capacitance fade. This increase is a direct consequence of the iodine/iodide redox pairs that strongly modifies the faradaic and non-faradaic type reactions occurring on the surface of the electrodes. Contrary to what is shown in few earlier reports, it is established that indiscriminate increase in the concentration of redox additives will leads to performance loss. Suitable explanations are given based on theoretical laws. The specific energy or power values being reported in the fabricated ASCs are comparable or higher than those reported in ASCs based on toxic acetonitrile or expensive ionic liquids. The paper shows that the use of redox additive is economically favorable strategy for obtaining cost effective and environmentally friendly ASCs.

  11. High energy density sodium-ion capacitors through co-intercalation mechanism in diglyme-based electrolyte system

    Science.gov (United States)

    Han, Pengxian; Han, Xiaoqi; Yao, Jianhua; Zhang, Lixue; Cao, Xiaoyan; Huang, Changshui; Cui, Gunglei

    2015-11-01

    A novel sodium-ion capacitor (NIC) was assembled using graphitic mesocarbon microbead anode and activated carbon cathode in diglyme-based electrolyte. Charge/discharge tests indicate that sodium ions can reversibly co-intercalated with diglyme solvent into graphite anode and show good rate performance. The energy densities of the NICs are as high as 93.5 and 86.5 Wh kg-1 at 573 and 2832 W kg-1 (equal to 4 C and 50 C) in the voltage window at 1-4 V, respectively. By optimizing the voltage ranges, the capacity retention of the NIC at 20 C is 98.3% even after 3000 cycles. Such superior electrochemical performance should be attributed to the reversible intercalated/deintercalated reaction of sodium ions and the formation of ternary graphite intercalation compounds in diglyme-based electrolyte. The present work pioneers new realms of hybrid energy storage system with high energy density, high power density and long cycle life.

  12. A hard X-ray photoelectron spectroscopy study on the solid electrolyte interphase of a lithium 4,5-dicyano-2-(trifluoromethyl)imidazolide based electrolyte for Si-electrodes

    Science.gov (United States)

    Lindgren, Fredrik; Xu, Chao; Maibach, Julia; Andersson, Anna M.; Marcinek, Marek; Niedzicki, Leszek; Gustafsson, Torbjörn; Björefors, Fredrik; Edström, Kristina

    2016-01-01

    This report focuses on the relatively new salt, lithium 4,5-dicyano-2-(trifluoromethyl)imidazolide (LiTDI), and its functionality together with a silicon based composite electrode in a half-cell lithium ion battery context. LiTDI is a promising alternative to the commonly used LiPF6 salt because it does not form HF which can decompose the oxide layer on Si. The formation of a solid electrolyte interphase (SEI) as well as the development of the active Si-particles are investigated during the first electrochemical lithiation and de-lithiation. Characterizations are carried out at different state of charge with scanning electron microscopy (SEM) as well as hard x-ray photoelectron spectroscopy (HAXPES) at two different photon energies. This enables a depth resolved picture of the reaction processes and gives an idea of the chemical buildup of the SEI. The SEI is formed by solvent and LiTDI decomposition products and its composition is similar to SEI formed by other carbonate based electrolytes. The LiTDI salt or its decomposition products are not in itself reactive towards the active Si-material and no unwanted side reactions occurs with the active Si-particles. Despite some decomposition of the LiTDI salt, it is a promising alternative for electrolytes aimed towards Si-based electrodes.

  13. All solid state lithium batteries based on lamellar garnet-type ceramic electrolytes

    Science.gov (United States)

    Du, Fuming; Zhao, Ning; Li, Yiqiu; Chen, Cheng; Liu, Ziwei; Guo, Xiangxin

    2015-12-01

    All solid-state lithium batteries are constructed by using highly conducting Ta-doped Li7La3Zr2O12 (LLZTO) as the solid electrolytes as well as the supports, coated with composite cathodes consisting of poly(vinylidene fluoride) (PVdF):LiTFSI, Ketjen Black, and carbon-coated LiFePO4 on one side and attached with Li anode on the other side. At 60 °C, the batteries show the first discharge capacity of 150 mAh g-1 at 0.05 C and 93% capacity retention after 100 cycles. As the current density increases from 0.05 C to 1 C, the specific capacity decreases from 150 mAh g-1 to 100 mAh g-1. Further elevated temperature up to 100 °C leads to further improved performance, i.e. 126 mAh g-1 at 1 C and 99% capacity retention after 100 cycles. This good performance can be attributed to the highly conducting ceramic electrolytes, the optimum electronic and ionic conducting networks in the composite cathodes, and closely contacted cathode/LLZTO interface. These results indicate that the present strategy is promising for development of high-performance solid-state Li-ion batteries operated at medium temperature.

  14. Preparation and characterization of high salts polymer electrolyte based on poly(lithium acrylate)

    Institute of Scientific and Technical Information of China (English)

    TANG Ai-dong; HUANG Ke-long; PAN Chun-yue; LU Cui-hong

    2005-01-01

    Novel polymer electrolytes were prepared by highly mixing poly(lithium acrylate)(PPALi) with eutectic lithium salts of lithium acetate and lithium nitrate.Poly(lithium acrylate) was preparaed by inverse emulsion polymerization from crylic acid and LiOH.Phase transition temperatures were measured for all the eutectic lithium of binary system samples as a function of the concentration of Li(CH3 COO),and the mixtures exhibit the lowest phase transition temperatures of (448±2) K at about 50% (mass fraction) Li(CH3 COO).Thermogravimetry(TG)and X-ray diffraction(XRD) analysis indicate the formation of a novel polymer-salt complex.The highest conductivity(approximately 4.97 ×10-5S·cm-1) is found at room temperature with the electrolyte composition of eutectic mixture of about 80% (mass fraction),poly(lithium acrylate) 20% under quickly cooling condition,which is 150%higher than that under natural cooling condition.

  15. Composite polymer electrolytes based on MG49 and carboxymethyl cellulose from kenaf

    Energy Technology Data Exchange (ETDEWEB)

    Jafirin, Serawati; Ahmad, Ishak; Ahmad, Azizan [Polymer Research Centre (PORCE), School of Chemical Science and Food Technology, Faculty of Science and Technology, Universiti Kebangsaan Malaysia, 43600, Bangi, Selangor Darul Ehsan (Malaysia)

    2013-11-27

    The development of 49% poly(methyl methacrylate)-grafted natural rubber (MG49) and carboxymethyl cellulose as a composite polymer electrolyte film incorporating LiCF{sub 3}SO{sub 3} were explored. Carboxymethyl cellulose was synthesized from kenaf bast fibres via carboxymethylation process by alkali catalyzed reaction of cellulose with sodium chloroacetate. Reflection fourier transform infrared (ATR-FTIR) spectroscopy showed the presence of carboxyl peak after modification of cellulose with sodium chloroacetate. X-ray diffraction (XRD) analysis revealed that the crystallinity of cellulose was decrease after synthesis. High performance composite polymer electrolytes were prepared with various composition of carboxymethyl cellulose (2–10 wt%) via solution-casting method. The conductivity was increased with carboxymethyl cellulose loading. The highest conductivity value achieved was 3.3 × 10{sup −7} Scm{sup −1} upon addition of 6% wt carboxymethyl cellulose. 6% wt carboxymethyl cellulose composition showed the highest tensile strength value of 7.9 MPa and 273 MPa of modulus value which demonstrated high mechanical performance with accepatable level of ionic conductivity.

  16. Synthesis and Ionic Conductivity of Siloxane Based Polymer Electrolytes with Propyl Butyrate Pendant Groups

    Energy Technology Data Exchange (ETDEWEB)

    Jalagonia, Natia; Tatrishvili, Tamara; Markarashvili, Eliza; Aneli, Jimsher; Mukbaniani, Omar [Javakhishvili Tbilisi State University, Tbilisi (Georgia); Grazulevicius, Jouzas Vidas [Kaunas University of Technology, Kaunas (Lithuania)

    2016-02-15

    Hydrosilylation reactions of 2.4.6.8-tetrahydro-2.4.6.8-tetramethylcyclotetrasiloxane with allyl butyrate catalyzed by Karstedt's, H2PtCl6 and Pt/C catalyst were studied and 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane was obtained. The reaction order, activation energies and rate constants were determined. Ringopening polymerization of 2.4.6.8-tetra (propyl butyrate)-2.4.6.8-tetramethylcyclotetrasiloxane in the presence of CaF2, LiF, KF and anhydrous potassium hydroxide in 60-70 .deg. C temperature range was carried out and methylsiloxane oligomers with regular arrangement of propyl butyrate pendant groups were obtained. The synthesized products were studied by FTIR and NMR spectroscopy. The polysiloxanes were characterized by wide-angle X-ray, gel-permeation chromatography and DSC analyses. Via sol-gel processes of oligomers doped with lithium trifluoromethylsulfonate or lithium bis (trifluoromethylsulfonyl)imide, solid polymer electrolyte membranes were obtained. The dependences of ionic conductivity of obtained polyelectrolytes on temperature and salt concentration were investigated, and it was shown that electric conductivity of the polymer electrolyte membranes at room temperature changed in the range 3.5x10{sup -4} - 6.4xa0{sup -7} S/cm.

  17. Studies on the structure and transport properties of hexanoyl chitosan-based polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Winie, Tan, E-mail: tanwinie@salam.uitm.edu.m [Faculty of Applied Sciences, Universiti Teknologi MARA, 40450 Shah Alam (Malaysia); Ramesh, S. [Faculty of Engineering and Science, University Tunku Abdul Rahman, 53300 Kuala Lumpur (Malaysia); Arof, A.K. [Physics Department, University of Malaya, 50603 Kuala Lumpur (Malaysia)

    2009-11-15

    Polymer electrolytes composed of hexanoyl chitosan as the host polymer, lithium trifluoromethanesulfonate (LiCF{sub 3}SO{sub 3}) as the salt, diethyl carbonate (DEC)/ethylene carbonate (EC) as the plasticizers were prepared and characterized by X-ray diffraction and impedance spectroscopy. The X-ray diffraction results reveal the variation in conductivity from structural aspect. This is reflected in terms of amorphous content. Sample with higher amorphous content exhibits higher conductivity. In order to further understand the source of the conductivity variation with varying plasticizers compositions as well as temperatures, the ionic charge carrier concentration and their mobility in polymer electrolyte were determined. The Rice and Roth model was proposed to be used to estimate the ionic charge carrier concentration, n. Knowing n and combining the result with dc conductivity, the mobility of the ionic charge carrier can be calculated. It is found that the conductivity change with DEC/EC composition is due mainly to the change in ionic charge carrier concentration while the conductivity change with temperature is due primarily to the change in mobility.

  18. Effect of mindfulness-based stress reduction on sleep quality

    DEFF Research Database (Denmark)

    Andersen, Signe; Würtzen, Hanne; Steding-Jessen, Marianne;

    2013-01-01

    The prevalence of sleep disturbance is high among cancer patients, and the sleep problems tend to last for years after the end of treatment. As part of a large randomized controlled clinical trial (the MICA trial, NCT00990977) of the effect of mindfulness-based stress reduction (MBSR) on psycholo......The prevalence of sleep disturbance is high among cancer patients, and the sleep problems tend to last for years after the end of treatment. As part of a large randomized controlled clinical trial (the MICA trial, NCT00990977) of the effect of mindfulness-based stress reduction (MBSR...

  19. The potential and challenges of thin-film electrolyte and nanostructured electrode for yttria-stabilized zirconia-base anode-supported solid oxide fuel cells

    Science.gov (United States)

    Noh, Ho-Sung; Yoon, Kyung Joong; Kim, Byung-Kook; Je, Hae-June; Lee, Hae-Weon; Lee, Jong-Ho; Son, Ji-Won

    2014-02-01

    Thin-film electrolytes and nanostructured electrodes are essential components for lowering the operation temperature of solid oxide fuel cells (SOFCs); however, reliably implementing thin-film electrolytes and nano-structure electrodes over a realistic SOFC platform, such as a porous anode-support, has been extremely difficult. If these components can be created reliably and reproducibly on porous substrates as anode supports, a more precise assessment of their impact on realistic SOFCs would be possible. In this work, structurally sound thin-film and nano-structured SOFC components consisting of a nano-composite NiO-yttria-stabilized zirconia (YSZ) anode interlayer, a thin YSZ and gadolinia-doped ceria (GDC) bi-layer electrolyte, and a nano-structure lanthanum strontium cobaltite (LSC)-base cathode, are sequentially fabricated on a porous NiO-YSZ anode support using thin-film technology. Using an optimized cell testing setup makes possible a more exact investigation of the potential and challenges of thin-film electrolyte and nanostructured electrode-based anode-supported SOFCs. Peak power densities obtained at 500 °C surpass 500 mW cm-2, which is an unprecedented low-temperature performance for the YSZ-based anode-supported SOFC. It is found that this critical, low-temperature performance for the anode-supported SOFC depends more on the electrode performance than the resistance of the thin-film electrolyte during lower temperature operation.

  20. Activated carbon and single-walled carbon nanotube based electrochemical capacitor in 1 M LiPF{sub 6} electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Azam, M.A., E-mail: asyadi@utem.edu.my [Carbon Research Technology Research Group, Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, Hang Tuah Jaya, 76100 Durian Tunggal, Melaka (Malaysia); Jantan, N.H.; Dorah, N.; Seman, R.N.A.R.; Manaf, N.S.A. [Carbon Research Technology Research Group, Faculty of Manufacturing Engineering, Universiti Teknikal Malaysia Melaka, Hang Tuah Jaya, 76100 Durian Tunggal, Melaka (Malaysia); Kudin, T.I.T. [Ionics Materials & Devices Research Laboratory, Faculty of Applied Sciences, Universiti Teknologi MARA, Shah Alam, Selangor (Malaysia); Yahya, M.Z.A. [Ionics Materials & Devices Research Laboratory, Faculty of Applied Sciences, Universiti Teknologi MARA, Shah Alam, Selangor (Malaysia); National Defence University of Malaysia, Kem Sungai Besi, 57000 Kuala Lumpur (Malaysia)

    2015-09-15

    Highlights: • Activated carbon and single-walled CNT based electrochemical capacitor. • Electrochemical analysis by means of CV, charge/discharge and impedance. • 1 M LiPF{sub 6} non-aqueous solution as an electrolyte. • AC/SWCNT electrode exhibits a maximum capacitance of 60.97 F g{sup −1}. - Abstract: Carbon nanotubes have been extensively studied because of their wide range of potential application such as in nanoscale electric circuits, textiles, transportation, health, and the environment. Carbon nanotubes feature extraordinary properties, such as electrical conductivities higher than those of copper, hardness and thermal conductivity higher than those of diamond, and strength surpassing that of steel, among others. This research focuses on the fabrication of an energy storage device, namely, an electrochemical capacitor, by using carbon materials, i.e., activated carbon and single-walled carbon nanotubes, of a specific weight ratio as electrode materials. The electrolyte functioning as an ion carrier is 1 M lithium hexafluorophosphate. Variations in the electrochemical performance of the device, including its capacitance, charge/discharge characteristics, and impedance, are reported in this paper. The electrode proposed in this work exhibits a maximum capacitance of 60.97 F g{sup −1} at a scan rate of 1 mV s{sup −1}.

  1. Activated carbon and single-walled carbon nanotube based electrochemical capacitor in 1 M LiPF6 electrolyte

    International Nuclear Information System (INIS)

    Highlights: • Activated carbon and single-walled CNT based electrochemical capacitor. • Electrochemical analysis by means of CV, charge/discharge and impedance. • 1 M LiPF6 non-aqueous solution as an electrolyte. • AC/SWCNT electrode exhibits a maximum capacitance of 60.97 F g−1. - Abstract: Carbon nanotubes have been extensively studied because of their wide range of potential application such as in nanoscale electric circuits, textiles, transportation, health, and the environment. Carbon nanotubes feature extraordinary properties, such as electrical conductivities higher than those of copper, hardness and thermal conductivity higher than those of diamond, and strength surpassing that of steel, among others. This research focuses on the fabrication of an energy storage device, namely, an electrochemical capacitor, by using carbon materials, i.e., activated carbon and single-walled carbon nanotubes, of a specific weight ratio as electrode materials. The electrolyte functioning as an ion carrier is 1 M lithium hexafluorophosphate. Variations in the electrochemical performance of the device, including its capacitance, charge/discharge characteristics, and impedance, are reported in this paper. The electrode proposed in this work exhibits a maximum capacitance of 60.97 F g−1 at a scan rate of 1 mV s−1

  2. Electric double-layer capacitors with tea waste derived activated carbon electrodes and plastic crystal based flexible gel polymer electrolytes

    Science.gov (United States)

    Suleman, M.; Deraman, M.; Othman, M. A. R.; Omar, R.; Hashim, M. A.; Basri, N. H.; Nor, N. S. M.; Dolah, B. N. M.; Hanappi, M. F. Y. M.; Hamdan, E.; Sazali, N. E. S.; Tajuddin, N. S. M.; Jasni, M. R. M.

    2016-08-01

    We report a novel configuration of symmetrical electric double-layer capacitors (EDLCs) comprising a plastic crystalline succinonitrile (SN) based flexible polymer gel electrolyte, incorporated with sodium trifluoromethane sulfonate (NaTf) immobilised in a host polymer poly (vinylidine fluoride-co-hexafluoropropylene) (PVdF-HFP). The cost-effective activated carbon powder possessing a specific surface area (SSA) of ~ 1700 m2g-1 containing a large proportion of meso-porosity has been derived from tea waste to use as supercapacitor electrodes. The high ionic conductivity (~3.6×10-3 S cm-1 at room temperature) and good electrochemical stability render the gel polymer electrolyte film a suitable candidate for the fabrication of EDLCs. The performance of the EDLCs has been tested by electrochemical impedance spectroscopy (EIS), cyclic voltammetry (CV), and galvanostatic charge-discharge studies. The performance of the EDLC cell is found to be promising in terms of high values of specific capacitance (~270 F g-1), specific energy (~ 36 Wh kg-1), and power density (~ 33 kW kg-1).

  3. Characteristics of the electrolytic amalgamation of trivalent f-elements and its application

    International Nuclear Information System (INIS)

    Based on reported radiopolarography data, the thermodynamic systematics of the aqueous electrolytic amalgamation of trivalent f-elements was studied. The free energy changes of alloy formation in an aqueous amalgamation system were compared with those in the pyrochemical reductive extraction system of Zn and Cd. It is shown that the free energy changes of mercury alloy formation by trivalent f-elements exhibits a unique dependency on the metallic radii. Using basic parameters of the electrolytic amalgamation of f-elements, the feasibility of the separation of Am and Cm from lanthanides by electrolytic amalgamation was studied. (orig.)

  4. A novel dimethyl sulfoxide/1,3-dioxolane based electrolyte for lithium/carbon fluorides batteries with a high discharge voltage plateau

    International Nuclear Information System (INIS)

    A novel dimethyl sulfoxide/1,3-dioxolane (DMSO/1,3-DO) based electrolyte is proposed for lithium/carbon fluorides (Li/CFx) batteries to enhance the discharge voltage plateau and energy density. Conductivities of the electrolyte of 1 mol L−1 LiBF4/DMSO+1,3-DO with different volume ratios are not identical, which have a maximum of 14.85 mS cm−1. From the tests of galvanostatic discharge, the discharge voltage plateau of the Li/CFx battery with an electrolyte of 1 mol L−1 LiBF4/DMSO+1,3-DO (5:5, v:v) can reach 2.69 V at 0.1 C, delivering a maximum discharge capacity of 831 mAh g−1 and the highest energy density of 2196 Wh kg−1. Compared to Li/CFx batteries with an electrolyte of 1 mol L−1 LiBF4/PC+DME (5:5, v:v), the energy density of Li/CFx batteries with an electrolyte of 1 mol L−1 LiBF4/DMSO+1,3-DO (5:5, v:v) has been improved more than 12%. With the help of XRD, SEM, TEM, EIS, FT-IR and GC-MS analysis, the results of this work suggest that DMSO/1,3-DO based electrolyte can significantly improve the discharge performance of Li/CFx batteries and keep a good electrochemical stability during discharge. The main reason for improvement of discharge performance is decreasing of both the overpotential of electrochemical polarization of CFx cathodes during discharge and the overpotential of ohmic polarization by increasing the ion conductivity of electrolyte

  5. Effects of different electrolytes on the electrochemical and dynamic behavior of electric double layer capacitors based on a porous silicon carbide electrode.

    Science.gov (United States)

    Kim, Myeongjin; Oh, Ilgeun; Kim, Jooheon

    2015-07-01

    Controlling the structure and morphology of porous electrode materials is an effective strategy for realizing a high surface area and efficient paths for ion diffusion. Moreover, excellent electrical conductivity can significantly decrease the internal resistance of an electrode by the formation of a conductive network and facilitate the application of electrostatic charges, which favors the accumulation of an electrical double layer. In light of these facts, we demonstrate the fabrication of β-polytype porous silicon carbide spheres (PSiCS) with a hierarchical pore structure in which micro- and mesopores are interconnected with a mesoporous network. Further, to investigate the effects of the electrolyte on the electrochemical and dynamic behavior, two-electrode symmetrical supercapacitors based on the PSiCS electrode with an aqueous electrolyte (1 M potassium chloride, KCl) or an organic electrolyte (1 M tetraethylammonium tetrafluoroborate in acetonitrile, TEABF4/AN) were assembled. The symmetrical supercapacitor based on the PSiCS electrode with the aqueous electrolyte exhibited a high charge-storage capacity with a specific capacitance of 82.9 F g(-1) at a scan rate of 5 mV s(-1), which is much higher than that obtained using the organic electrolyte (60.3 F g(-1) at a scan rate of 5 mV s(-1)). However, the energy density of the organic electrolyte system was 102.59 W h kg(-1) at a scan rate of 5 mV s(-1), which is greatly superior to that of the aqueous electrolyte system (energy density: 29.47 W h kg(-1)) owing to the wide cell operating voltage range. PMID:26051533

  6. Polymer Electrolytes for Lithium/Sulfur Batteries

    Directory of Open Access Journals (Sweden)

    The Nam Long Doan

    2012-08-01

    Full Text Available This review evaluates the characteristics and advantages of employing polymer electrolytes in lithium/sulfur (Li/S batteries. The main highlights of this study constitute detailed information on the advanced developments for solid polymer electrolytes and gel polymer electrolytes, used in the lithium/sulfur battery. This includes an in-depth analysis conducted on the preparation and electrochemical characteristics of the Li/S batteries based on these polymer electrolytes.

  7. Hexanoyl Chitosan-based Gel Electrolyte for Lithium-ion Cell

    Institute of Scientific and Technical Information of China (English)

    Tan Winie; A.K. Arof

    2005-01-01

    @@ 1Introduction Chitosan is soluble in dilute acid solutions as a result of salt formation by the amino groups with various inorganic and organic acids[1,2]. Due to the reactivity of water and other protic solvents such as methanol and acetic acid with the electrode material in the lithiumbased electrochemicaldevices[3], the insolubility of chitosan in aprotic solvents is inadequate to meet the requirements to be used as the electrolyte materials. In order to improve its solubility in aprotic solvents,acyl modification of chitosan was carried out in the present study.Hexanoyl-chitosan (Fig. 1) that exhibited solubility in THF was prepared by reacting the chitosan with hexanoyl chloride in a mixture of pyridine and THF[4].

  8. Advances in lithium-sulfur batteries based on multifunctional cathodes and electrolytes

    Science.gov (United States)

    Pang, Quan; Liang, Xiao; Kwok, Chun Yuen; Nazar, Linda F.

    2016-09-01

    Amid burgeoning environmental concerns, electrochemical energy storage has rapidly gained momentum. Among the contenders in the ‘beyond lithium’ energy storage arena, the lithium-sulfur (Li-S) battery has emerged as particularly promising, owing to its potential to reversibly store considerable electrical energy at low cost. Whether or not Li-S energy storage will be able to fulfil this potential depends on simultaneously solving many aspects of its underlying conversion chemistry. Here, we review recent developments in tackling the dissolution of polysulfides — a fundamental problem in Li-S batteries — focusing on both experimental and computational approaches to tailor the chemical interactions between the sulfur host materials and polysulfides. We also discuss smart cathode architectures enabled by recent materials engineering, especially for high areal sulfur loading, as well as innovative electrolyte design to control the solubility of polysulfides. Key factors that allow long-life and high-loading Li-S batteries are summarized.

  9. Ionic transport and electrochemical stability of PVDF-HFP based gel polymer electrolytes

    Science.gov (United States)

    Rosdi, A.; Zainol, N. H.; Osman, Z.

    2016-02-01

    The gel polymer electrolytes (GPEs) samples consisting of polyvinylidenefluoride-co-hexafluoropropylene (PVDF-HFP), ethylene carbonate (EC) and propylene carbonate (PC) with different concentrations of magnesium triflate salt, Mg(CF3SO3)2 were prepared using the solution casting technique. The ionic conductivity of the GPEs was studied by using a.c impedance spectroscopy and the sample containing 20 wt% salt exhibited the highest conductivity of 5.11 × l0-3 Scm-1. Ionic transport number of the GPEs shows that the samples contain ionic species as main charge carrier while cationic transport number for the highest conducting sample was found to be 0.27. The electrochemical properties of the GPEs were studied using Linear Sweep Voltammetry (LSV) and Cyclic Voltammetry (CV). The GPEs show high electrochemical stability ˜3.5V (versus Mg2+/Mg) where the highest conducting sample exhibited the highest stability.

  10. Advances in lithium–sulfur batteries based on multifunctional cathodes and electrolytes

    Science.gov (United States)

    Pang, Quan; Liang, Xiao; Kwok, Chun Yuen; Nazar, Linda F.

    2016-09-01

    Amid burgeoning environmental concerns, electrochemical energy storage has rapidly gained momentum. Among the contenders in the ‘beyond lithium’ energy storage arena, the lithium–sulfur (Li–S) battery has emerged as particularly promising, owing to its potential to reversibly store considerable electrical energy at low cost. Whether or not Li–S energy storage will be able to fulfil this potential depends on simultaneously solving many aspects of its underlying conversion chemistry. Here, we review recent developments in tackling the dissolution of polysulfides — a fundamental problem in Li–S batteries — focusing on both experimental and computational approaches to tailor the chemical interactions between the sulfur host materials and polysulfides. We also discuss smart cathode architectures enabled by recent materials engineering, especially for high areal sulfur loading, as well as innovative electrolyte design to control the solubility of polysulfides. Key factors that allow long-life and high-loading Li–S batteries are summarized.

  11. Power capability of LiTDI-based electrolytes for lithium-ion batteries

    Science.gov (United States)

    Paillet, Sabrina; Schmidt, Gregory; Ladouceur, Sébastien; Fréchette, Joël; Barray, Francis; Clément, Daniel; Hovington, Pierre; Guerfi, Abdelbast; Vijh, Ashok; Cayrefourcq, Ian; Zaghib, Karim

    2015-10-01

    We report results obtained with lithium 4,5-dicyano-2-(trifluoromethyl) imidazolide (LiTDI), which we believe is a promising lithium salt for electrolytes in lithium-ion batteries. This "Hückel"- type salt has high charge delocalizations which contribute to good lithium-ion dissociation. In addition, it has high thermal stability and safer degradation products compared to LiPF6, which were identified by TGA-MS. It also does not corrode but passivate the aluminum current collector. Cyclic voltammetry measurements showed a stability up to 4.5 V, which is sufficient for use with standard cathode materials. The power capability of half cells containing LiTDI in EC/DEC was evaluated with standard cathodes used in lithium-ion batteries: LFP, NMC, LCO and LMO. Two LiTDI concentrations were investigated: 1 M and 0.6 M and compared with a reference electrolyte: 1 M LiPF6. In spite of a slightly lower conductivity than the LiPF6, LiTDI (1 M and 0.6 M) shows similar power capability up to 2C with LFP (84% of specific capacity recovered), 10C with NMC (61% of specific capacity recovered), and up to 20C for LMO (88% of specific capacity recovered). Furthermore, better power capability was obtained with 0.6 M LiTDI with LCO, which yielded 82% of specific capacity recovered at 1C (67% for 1 M LiTDI and 1 M LiPF6).

  12. A novel PEO-based composite polymer electrolyte with absorptive glass mat for Li-ion batteries

    International Nuclear Information System (INIS)

    A novel PEO (polyethylene oxide)-based composite polymer electrolyte (CPE) using absorptive glass mat (AGM) as filler was prepared and characterized. Scanning electronic micrograph (SEM) images showed that the addition of Li salt and modified AGM may improve the surface morphology of CPE. The results of Fourier-transform infrared (FTIR) spectroscopy, X-ray diffraction (XRD) and differential scanning calorimeters (DSC) indicated that the inclusion of LiClO4 salt and the addition of AGM filler can reduce the crystallinity of PEO. It was concluded that the addition of AGM plays two roles in PEO-based CPEs, namely, interruption of the PEO recrystallization and reinforcement of CPEs, accordingly enhancing room temperature ionic conductivity of CPEs and improving its mechanical strength and electrochemical stability at high temperatures

  13. Calculation of constants of acid-base equilibria at the oxide-electrolyte interface from electrokinetic potential dependence on pH

    International Nuclear Information System (INIS)

    Method is proposed for calculating the constants of acid-base equilibria at the oxide-electrolyte interface. The method is based on the electrokinetic potential dependence on ph value at different electrolyte concentrations. It is shown that the calculated constant values for La2O3 and ZrO2 equal correspondingly 7.3 and 3.9 (pK10); 11.9 and 9.1 (pK20); 9.2 and 5.8 (pK30); 10.0 and 7.2 (pK40) agree well with literature data. 21 refs.; 3 figs.; 3 tabs

  14. Toward 5 V Li-Ion Batteries: Quantum Chemical Calculation and Electrochemical Characterization of Sulfone-Based High-Voltage Electrolytes.

    Science.gov (United States)

    Wu, Feng; Zhou, Hang; Bai, Ying; Wang, Huali; Wu, Chuan

    2015-07-15

    In seeking new sulfone-based electrolytes to meet the demand of 5 V lithium-ion batteries, we have combined the theoretical quantum chemistry calculation and electrochemical characterization to explore several sulfone/cosolvent systems. Tetramethylene sulfone (TMS), dimethyl sulfite (DMS), and diethyl sulfite (DES) were used as solvents, and three kinds of lithium salts including LiBOB, LiTFSI, and LiPF6 were added into TMS/DMS [1:1, (v)] and TMS/DES [1:1, (v)] to form high-voltage electrolyte composites, respectively. All of these electrolytes display wide electrochemical windows of more than 5.4 V, with the high electrolyte conductivities being more than 3 mS/cm at room temperature. It is indicated that to achieve the best ionic conductivity in TMS/DMS cosolvent, the optimized concentrations of lithium salts LiBOB, LiTFSI, and LiPF6 were 0.8, 1, and 1 M, respectively. Furthermore, the vibrational changes of the molecular functional groups in the cosolvents were evaluated by Fourier transform infrared spectroscopy. It is found that lithium salts show strong interaction with the main functional sulfone groups and sulfonic acid ester group, thus playing a vital role in the enhancement of the ionic conductivity and electrochemical stability of the solvent system. These sulfone-based solvents with high electrochemical stability are expected to become a new generation of a high-voltage organic electrolytic liquid system for lithium-ion batteries. PMID:26087246

  15. SEI Formation and Interfacial Stability of a Si Electrode in a LiTDI-Salt Based Electrolyte with FEC and VC Additives for Li-Ion Batteries.

    Science.gov (United States)

    Lindgren, Fredrik; Xu, Chao; Niedzicki, Leszek; Marcinek, Marek; Gustafsson, Torbjörn; Björefors, Fredrik; Edström, Kristina; Younesi, Reza

    2016-06-22

    An electrolyte based on the new salt, lithium 4,5-dicyano-2-(trifluoromethyl)imidazolide (LiTDI), is evaluated in combination with nano-Si composite electrodes for potential use in Li-ion batteries. The additives fluoroethylene carbonate (FEC) and vinylene carbonate (VC) are also added to the electrolyte to enable an efficient SEI formation. By employing hard X-ray photoelectron spectroscopy (HAXPES), the SEI formation and the development of the active material is probed during the first 100 cycles. With this electrolyte formulation, the Si electrode can cycle at 1200 mAh g(-1) for more than 100 cycles at a coulombic efficiency of 99%. With extended cycling, a decrease in Si particle size is observed as well as an increase in silicon oxide amount. As opposed to LiPF6 based electrolytes, this electrolyte or its decomposition products has no side reactions with the active Si material. The present results further acknowledge the positive effects of SEI forming additives. It is suggested that polycarbonates and a high LiF content are favorable components in the SEI over other kinds of carbonates formed by ethylene carbonate (EC) and dimethyl carbonate (DMC) decomposition. This work thus confirms that LiTDI in combination with the investigated additives is a promising salt for Si electrodes in future Li-ion batteries. PMID:27220376

  16. CuZn Alloy- Based Electrocatalyst for CO2 Reduction

    KAUST Repository

    Alazmi, Amira

    2014-06-01

    ABSTRACT CuZn Alloy- Based Electrocatalyst for CO2 Reduction Amira Alazmi Carbon dioxide (CO2) is one of the major greenhouse gases and its emission is a significant threat to global economy and sustainability. Efficient CO2 conversion leads to utilization of CO2 as a carbon feedstock, but activating the most stable carbon-based molecule, CO2, is a challenging task. Electrochemical conversion of CO2 is considered to be the beneficial approach to generate carbon-containing fuels directly from CO2, especially when the electronic energy is derived from renewable energies, such as solar, wind, geo-thermal and tidal. To achieve this goal, the development of an efficient electrocatalyst for CO2 reduction is essential. In this thesis, studies on CuZn alloys with heat treatments at different temperatures have been evaluated as electrocatalysts for CO2 reduction. It was found that the catalytic activity of these electrodes was strongly dependent on the thermal oxidation temperature before their use for electrochemical measurements. The polycrystalline CuZn electrode without thermal treatment shows the Faradaic efficiency for CO formation of only 30% at applied potential ~−1.0 V vs. RHE with current density of ~−2.55 mA cm−2. In contrast, the reduction of oxide-based CuZn alloy electrode exhibits 65% Faradaic efficiency for CO at lower applied potential about −1.0 V vs. RHE with current density of −2.55 mA cm−2. Furthermore, stable activity was achieved over several hours of the reduction reaction at the modified electrodes. Based on electrokinetic studies, this improvement could be attributed to further stabilization of the CO2•− on the oxide-based Cu-Zn alloy surface.

  17. Harmonic Reduction In Five Level Inverter Based Dynamic Voltage Restorer

    Directory of Open Access Journals (Sweden)

    S. Leela

    2010-12-01

    Full Text Available This study deals with harmonic reduction in the five level inverter based Dynamic Voltage Restorer(DVR. The control of DV R that injects a voltage in series with a distribution feeder is presented. DVR is a power electronic controller that can protect sensitive loads from disturbances in supply system. DVR can regulate the voltage at the load. The simulation results of five level inverter based DVR are presented. The spectrum for the output voltage is also presented.

  18. Ion chromatography electrospray ionization mass spectrometry method development and investigation of lithium hexafluorophosphate-based organic electrolytes and their thermal decomposition products.

    Science.gov (United States)

    Kraft, Vadim; Grützke, Martin; Weber, Waldemar; Winter, Martin; Nowak, Sascha

    2014-08-01

    A method based on the coupling of ion chromatography (IC) and electrospray ionization mass spectrometry (ESI-MS) for the separation and determination of thermal decomposition products of LiPF6-based organic electrolytes is presented. The utilized electrolytes, LP30 and LP50, are commercially available and consist of 1mol/l LiPF6 dissolved in ethylene carbonate/dimethyl carbonate and ethylene carbonate/ethyl methyl carbonate, respectively. For the separation method development three ion chromatographic columns with different capacity and stationary phase were used and compared. Besides the known hydrolysis products of lithium hexafluorophosphate, several new organophosphates were separated and identified with the developed IC-ESI-MS method during aging investigations of the electrolytes. The chemical structures were elucidated with IC-ESI-MS/MS. PMID:24939088

  19. Optimization of a carbon-based hybrid energy storage device with cerium (III) sulfate as redox electrolyte

    Science.gov (United States)

    Díaz, Patricia; González, Zoraida; Santamaría, Ricardo; Granda, Marcos; Menéndez, Rosa; Blanco, Clara

    2016-03-01

    The electrochemical performance of a carbon-based hybrid energy storage system, with Ce2(SO4)3/H2SO4 as inorganic redox electrolyte, was enhanced by optimizing several parameters of the device. A mass balance of the two electrodes forming the system together with the selection of a suitable activated carbon as negative electrode allowed the cell voltage to be increased up to 1.9 V. In addition, the use of a cation-exchange membrane significantly enhanced the electrochemical performance of the system by minimizing secondary reactions of cerium ions on the negative electrode. The optimized device reached energy and power density values up to ∼20 W h kg-1 and 524 W kg-1 respectively. Moreover, the system showed a good long-term electrochemical performance over 20,000 cycles.

  20. Investigation Of Hydrogen Production By Using Composite Membrane (Nafion/Zro2-Based Solid Polymer Electrolyte Water Electrolyser

    Directory of Open Access Journals (Sweden)

    E.L.Santhi priyaa ,

    2015-05-01

    Full Text Available In the present study, Composite materials based on perfluorinated cation-exchange membrane incorporating particles of Zirconium and Nafion is synthesized .With this membrane the performance of the electrolysis cell improved considerably at room temperature and atmospheric pressure. In addition, by using catalysts and membranes, the performance of this Composite membrane is studied by varying voltage range with respect to hydrogen yield and at current density 0.1, 0.2, 0.3, 0.4, and 0.5(A cm-2 , With a Nafion 115 membrane as a reference electrolyte. Experiments have shown that 99.9% purity of hydrogen Gas is evolved The physicochemical properties of the composite membranes such as thermogravimetric analyzer (TGA, Scanning Electron Microscope (SEM, XRD (X-ray powder diffraction, Fourier transform infrared spectroscopyand and Ion Exchange Capacity is determined. The fabricated composite membranes have shown the significant improvement of all tested properties compared to that of pure Nafion membrane.

  1. A redox-flow battery with an alloxazine-based organic electrolyte

    Science.gov (United States)

    Lin, Kaixiang; Gómez-Bombarelli, Rafael; Beh, Eugene S.; Tong, Liuchuan; Chen, Qing; Valle, Alvaro; Aspuru-Guzik, Alán; Aziz, Michael J.; Gordon, Roy G.

    2016-09-01

    Redox-flow batteries (RFBs) can store large amounts of electrical energy from variable sources, such as solar and wind. Recently, redox-active organic molecules in aqueous RFBs have drawn substantial attention due to their rapid kinetics and low membrane crossover rates. Drawing inspiration from nature, here we report a high-performance aqueous RFB utilizing an organic redox compound, alloxazine, which is a tautomer of the isoalloxazine backbone of vitamin B2. It can be synthesized in high yield at room temperature by single-step coupling of inexpensive o-phenylenediamine derivatives and alloxan. The highly alkaline-soluble alloxazine 7/8-carboxylic acid produces a RFB exhibiting open-circuit voltage approaching 1.2 V and current efficiency and capacity retention exceeding 99.7% and 99.98% per cycle, respectively. Theoretical studies indicate that structural modification of alloxazine with electron-donating groups should allow further increases in battery voltage. As an aza-aromatic molecule that undergoes reversible redox cycling in aqueous electrolyte, alloxazine represents a class of radical-free redox-active organics for use in large-scale energy storage.

  2. Characterization and electrical properties of polyvinyl alcohol based polymer electrolyte films doped with ammonium thiocyanate

    International Nuclear Information System (INIS)

    Highlights: • Polyvinyl alcohol (PVA). • Ammonium thiocyanate (NH4SCN). • Electrical conductivity. • Fractals. - Abstract: In this communication, films of polyvinyl alcohol (PVA) polymer complexed with ammonium thiocyanate (NH4SCN) salt were studied. XRD (X-ray diffraction) was used to study the complexation of salt with the polymer matrix and amorphicity in the films. DSC (differential scanning calorimetry) studies showed that the glass transition temperatures (Tg) of the PVA:NH4SCN complexed films were less than pristine PVA. Raman analysis was analyzed in order to study the change in the vibrational bands due to the complexation of salt with PVA. Optical micrographs confirm the fractal formation in 75:25 and 70:30 PVA:NH4SCN films. Ionic transference number was estimated by Wagner's polarization method and its large value indicates that conduction takes place mainly due to mobile ionic species. Maximum conductivity ∼10−3 S/cm at room temperature was obtained for 70:30 ratio of PVA: NH4SCN polymer electrolyte films

  3. Center for BioBased Binders and Pollution Reduction Technology

    Energy Technology Data Exchange (ETDEWEB)

    Thiel, Jerry [Univ. of Northern Iowa, Cedar Falls, IA (United States)

    2013-07-01

    Funding will support the continuation of the Center for Advanced Bio-based Binders and Pollution Reduction Technology Center (CABB) in the development of bio-based polymers and emission reduction technologies for the metal casting industry. Since the formation of the center several new polymers based on agricultural materials have been developed. These new materials have show decreases in hazardous air pollutants, phenol and formaldehyde as much as 50 to 80% respectively. The polymers termed bio-polymers show a great potential to utilize current renewable agricultural resources to replace petroleum based products and reduce our dependence on importing of foreign oil. The agricultural technology has shown drastic reductions in the emission of hazardous air pollutants and volatile organic compounds and requires further development to maintain competitive costs and productivity. The project will also research new and improved inorganic binders that promise to eliminate hazardous emissions from foundry casting operations and allow for the beneficial reuse of the materials and avoiding the burdening of overcrowded landfills.

  4. Enhanced photoelectric performance in self-powered UV detectors based on ZnO nanowires with plasmonic Au nanoparticles scattered electrolyte

    Science.gov (United States)

    Zeng, Yiyu; Ye, Zhizhen; Lu, Bin; Dai, Wei; Pan, Xinhua

    2016-04-01

    Vertically aligned ZnO nanowires (NWs) were grown on a fluorine-doped tin-oxide-coated glass substrate by a hydrothermal method. Au nanoparticles were well dispersed in the mixed solution of ethanol and deionized water. A simple self-powered ultraviolet detector based on solid-liquid heterojunction was fabricated, utilizing ZnO NWs as active photoanode and such prepared mixed solution as electrolyte. The introduction of Au nanoparticles results in considerable improvements in the responsivity and sensitivity of the device compared with the one using deionized water as electrolyte, which is attributed to the enhanced light harvesting by Au nanoparticles.

  5. Statistical detection of structural damage based on model reduction

    Institute of Scientific and Technical Information of China (English)

    Tao YIN; Heung-fai LAM; Hong-ping ZHU

    2009-01-01

    This paper proposes a statistical method for damage detection based on the finite element (FE) model reduction technique that utilizes measured modal data with a limited number of sensors.A deterministic damage detection process is formulated based on the model reduction technique.The probabilistic process is integrated into the deterministic damage detection process using a perturbation technique,resulting in a statistical structural damage detection method.This is achieved by deriving the firstand second-order partial derivatives of uncertain parameters,such as elasticity of the damaged member,with respect to the measurement noise,which allows expectation and covariance matrix of the uncertain parameters to be calculated.Besides the theoretical development,this paper reports numerical verification of the proposed method using a portal frame example and Monte Carlo simulation.

  6. First application of diethyl oxalate as efficient additive in high performance dye-sensitized solar cells based on iodide/triiodide electrolyte

    International Nuclear Information System (INIS)

    In this study, diethyl oxalate (DEOX) is applied as an effective inexpensive additive based iodide/triiodide electrolyte in the dye-sensitized solar cells (DSSCs). Addition the suitable amount of DEOX as 1 M into the electrolyte shows dramatically improvement in the short circuit current (Jsc) and consequently, in the total conversion efficiency (η). The fabricated devices based on N719 and 2-cyano-3-(4-(diphenylamino) phenyl) acrylic acid (TPA) sensitizers with modified electrolyte show the efficiency of 7.33% and 2.63% at an irradiation of AM1.5, and an 37% and 22% energy conversion efficiency increments, respectively. The boost in the photocurrent density mainly is due to the molecular complex formation between DEOX and redox species in the electrolyte solution that promotes the electrochemical properties of electrolyte. Also, electrochemical impedance measurements indicate adsorbing of DEOX on the semiconductor surface leads to an incensement in the lifetime (τ) and the electron density (ns) in the conduction band (CB) of TiO2 that shifts the Fermi level (EF) which leads to small enhancement in the Voc. Adsorbing of DEOX on the titania surface retards the interfacial charge recombination that has a beneficial effect on the Voc and Jsc. Furthermore, we compares the effect mechanisms of DEOX and 4-tert-butylpyridine (TBP) additives on the cell performance by applying different electrolytes containing the additives. These results show that TBP increases Voc while DEOX additive has effect on the Jsc and using of combination of additives leads to a remarkable improvement in η. As a result, DEOX is a new promising co-additive which can be used for high efficient and low cost DSSCs

  7. Annealing Would Improve beta" - Alumina Solid Electrolyte

    Science.gov (United States)

    Williams, Roger; Homer, Margie; Ryan, Margaret; Cortez, Roger; Shields, Virgil; Kisor, Adam

    2003-01-01

    A pre-operational annealing process is under investigation as a potential means of preventing a sudden reduction of ionic conductivity in a Beta"-alumina solid electrolyte (BASE) during use. On the basis of tests, the sudden reduction of ionic conductivity, followed by a slow recovery, has been found to occur during testing of the solid electrolyte and electrode components of an alkali metal thermal-to-electric converter (AMTEC) cell. At this time, high-temperature tests of limited duration have indicated the superiority of the treated BASE, but reproducible tests over thousands of hours are necessary to confirm that microcracking has been eliminated. The ionic conductivity of the treated BASE is also measured to be higher than untreated BASE at 1,073 K in low-pressure sodium vapor. Microcracking resulting in loss of conductivity was not observed with treated BASE in one high-temperature experiment, but this result must be duplicated over very long testing times to be sure of the effect. Shorter annealing times (10 to 20 hours) were found to result in significantly less loss of mass; it may be necessary for the packed powder mixture to evolve some Na2O before the Na2O can leave the ceramic.

  8. Effects of dietary electrolyte balance and molasses in diets with corn-based distiller's dried grains with solubles on growth performance in nursery and finishing pigs

    Science.gov (United States)

    Two assays were conducted to determine the effects of dietary electrolyte balance dEB) and molasses in diets with corn-based distiller’s dried grains with solubles (DDGS, Sioux River Ethanol, Hudson, SD) on growth performance of nursery and finishing pigs. For the first experiment, 126 nursery pigs ...

  9. Effect of swift heavy O7+ ion radiations on conductivity of lithium based polymer blend electrolyte

    International Nuclear Information System (INIS)

    In the present work, effect of swift heavy O7+ ion of 80 MeV of different fluences, on conductivity of [PVA(47.5)–PEO(47.5)–LiCF3SO3(5)]–EC(8) polymeric films has been investigated using ac impedance spectroscopy. The power law exponent n, hopping frequency ωh and activation energies for conduction Eac and relaxation Ear, have been investigated for different fluences. The DSC measurements are carried out in order to investigate the variations in the degree of crystallinity and thermal parameters (Tm) of the blend specimen prior and after irradiation. The Fourier Transform Infrared (FT-IR) measurements are carried out in order to investigate the changes in the vibrational modes of molecules upon irradiation. The FT-IR measurements corroborate the formation of amorphous phase in the blend matrix after irradiation. The conductivity is found to be optimum at the fluence of 1×1012 ions/cm2. The enhancement and the improvement in the electrolytic properties of PVA–PEO blend upon O7+ ion irradiation have been observed. - Highlights: • dc Conductivity of PVA–PEO blend system gets improved upon irradiation. • The specimen irradiated at a fluence of 1×1012 ions/cm2 shows the optimum value of conductivity. • The values of melting temperatures change with varying fluences of radiations. • The conduction and relaxation activation energies at various fluences are comparable. • After irradiation, the degree of crystallinity reduces, but no structural changes are observed

  10. Improved power conversion efficiency of dye-sensitized solar cells using side chain liquid crystal polymer embedded in polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Cho, Woosum [Department of Chemistry Education, and Department of Frontier Materials Chemistry, and Institute for Plastic Information and Energy Materials, Pusan National University, Busan 609-735 (Korea, Republic of); Lee, Jae Wook, E-mail: jlee@donga.ac.kr [Department of Chemistry, Dong-A University, Busan 604-714 (Korea, Republic of); Gal, Yeong-Soon [Polymer Chemistry Lab, College of General Education, Kyungil University, Hayang 712-701 (Korea, Republic of); Kim, Mi-Ra, E-mail: mrkim2@pusan.ac.kr [Department of Polymer Science and Engineering, Pusan National University, Busan 609-735 (Korea, Republic of); Jin, Sung Ho, E-mail: shjin@pusan.ac.kr [Department of Chemistry Education, and Department of Frontier Materials Chemistry, and Institute for Plastic Information and Energy Materials, Pusan National University, Busan 609-735 (Korea, Republic of)

    2014-02-14

    Side chain liquid crystal polymer (SCLCP) embedded in poly(vinylidenefluoride-co-hexafluoropropylene) (PVdF-co-HFP)-based polymer electrolytes (PVdF-co-HFP:side chain liquid crystal polymer (SCLCP)) was prepared for dye-sensitized solar cell (DSSC) application. The polymer electrolytes contained tetrabutylammonium iodide (TBAI), iodine (I{sub 2}), and 8 wt% PVdF-co-HFP in acetonitrile. DSSCs comprised of PVdF-co-HFP:SCLCP-based polymer electrolytes displayed enhanced redox couple reduction and reduced charge recombination in comparison to those of the conventional PVdF-co-HFP-based polymer electrolyte. The significantly increased short-circuit current density (J{sub sc}, 10.75 mA cm{sup −2}) of the DSSCs with PVdF-co-HFP:SCLCP-based polymer electrolytes afforded a high power conversion efficiency (PCE) of 5.32% and a fill factor (FF) of 0.64 under standard light intensity of 100 mW cm{sup −2} irradiation of AM 1.5 sunlight. - Highlights: • We developed the liquid crystal polymer embedded on polymer electrolyte for DSSCs. • We fabricated the highly efficient DSSCs using polymer electrolyte. • The best PCE achieved for P1 is 5.32% using polymer electrolyte.

  11. A POCS-Based Algorithm for Blocking Artifacts Reduction

    Institute of Scientific and Technical Information of China (English)

    ZHAO Yi-hong; CHENG Guo-hua; YU Song-yu

    2006-01-01

    An algorithm for blocking artifacts reduction in DCT domain for block-based image coding was developed. The algorithm is based on the projection onto convex set (POCS) theory. Due to the fact that the DCT characteristics of shifted blocks are different caused by the blocking artifacts, a novel smoothness constraint set and the corresponding projection operator were proposed to reduce the blocking artifacts by discarding the undesired high frequency coefficients in the shifted DCT blocks. The experimental results show that the proposed algorithm outperforms the conventional algorithms in terms of objective quality, subjective quality, and convergence property.

  12. Programmed emulsions for sodium reduction in emulsion based foods.

    Science.gov (United States)

    Chiu, Natalie; Hewson, Louise; Fisk, Ian; Wolf, Bettina

    2015-05-01

    In this research a microstructure approach to reduce sodium levels in emulsion based foods is presented. If successful, this strategy will enable reduction of sodium without affecting consumer satisfaction with regard to salty taste. The microstructure approach comprised of entrapment of sodium in the internal aqueous phase of water-in-oil-in-water emulsions. These were designed to destabilise during oral processing when in contact with the salivary enzyme amylase in combination with the mechanical manipulation of the emulsion between the tongue and palate. Oral destabilisation was achieved through breakdown of the emulsion that was stabilised with a commercially modified octenyl succinic anhydride (OSA)-starch. Microstructure breakdown and salt release was evaluated utilising in vitro, in vivo and sensory methods. For control emulsions, stabilised with orally inert proteins, no loss of structure and no release of sodium from the internal aqueous phase was found. The OSA-starch microstructure breakdown took the initial form of oil droplet coalescence. It is hypothesised that during this coalescence process sodium from the internalised aqueous phase is partially released and is therefore available for perception. Indeed, programmed emulsions showed an enhancement in saltiness perception; a 23.7% reduction in sodium could be achieved without compromise in salty taste (p < 0.05; 120 consumers). This study shows a promising new approach for sodium reduction in liquid and semi-liquid emulsion based foods. PMID:25865459

  13. Programmed emulsions for sodium reduction in emulsion based foods.

    Science.gov (United States)

    Chiu, Natalie; Hewson, Louise; Fisk, Ian; Wolf, Bettina

    2015-05-01

    In this research a microstructure approach to reduce sodium levels in emulsion based foods is presented. If successful, this strategy will enable reduction of sodium without affecting consumer satisfaction with regard to salty taste. The microstructure approach comprised of entrapment of sodium in the internal aqueous phase of water-in-oil-in-water emulsions. These were designed to destabilise during oral processing when in contact with the salivary enzyme amylase in combination with the mechanical manipulation of the emulsion between the tongue and palate. Oral destabilisation was achieved through breakdown of the emulsion that was stabilised with a commercially modified octenyl succinic anhydride (OSA)-starch. Microstructure breakdown and salt release was evaluated utilising in vitro, in vivo and sensory methods. For control emulsions, stabilised with orally inert proteins, no loss of structure and no release of sodium from the internal aqueous phase was found. The OSA-starch microstructure breakdown took the initial form of oil droplet coalescence. It is hypothesised that during this coalescence process sodium from the internalised aqueous phase is partially released and is therefore available for perception. Indeed, programmed emulsions showed an enhancement in saltiness perception; a 23.7% reduction in sodium could be achieved without compromise in salty taste (p sodium reduction in liquid and semi-liquid emulsion based foods.

  14. Sound reduction by metamaterial-based acoustic enclosure

    International Nuclear Information System (INIS)

    In many practical systems, acoustic radiation control on noise sources contained within a finite volume by an acoustic enclosure is of great importance, but difficult to be accomplished at low frequencies due to the enhanced acoustic-structure interaction. In this work, we propose to use acoustic metamaterials as the enclosure to efficiently reduce sound radiation at their negative-mass frequencies. Based on a circularly-shaped metamaterial model, sound radiation properties by either central or eccentric sources are analyzed by numerical simulations for structured metamaterials. The parametric analyses demonstrate that the barrier thickness, the cavity size, the source type, and the eccentricity of the source have a profound effect on the sound reduction. It is found that increasing the thickness of the metamaterial barrier is an efficient approach to achieve large sound reduction over the negative-mass frequencies. These results are helpful in designing highly efficient acoustic enclosures for blockage of sound in low frequencies

  15. Sound reduction by metamaterial-based acoustic enclosure

    Directory of Open Access Journals (Sweden)

    Shanshan Yao

    2014-12-01

    Full Text Available In many practical systems, acoustic radiation control on noise sources contained within a finite volume by an acoustic enclosure is of great importance, but difficult to be accomplished at low frequencies due to the enhanced acoustic-structure interaction. In this work, we propose to use acoustic metamaterials as the enclosure to efficiently reduce sound radiation at their negative-mass frequencies. Based on a circularly-shaped metamaterial model, sound radiation properties by either central or eccentric sources are analyzed by numerical simulations for structured metamaterials. The parametric analyses demonstrate that the barrier thickness, the cavity size, the source type, and the eccentricity of the source have a profound effect on the sound reduction. It is found that increasing the thickness of the metamaterial barrier is an efficient approach to achieve large sound reduction over the negative-mass frequencies. These results are helpful in designing highly efficient acoustic enclosures for blockage of sound in low frequencies.

  16. Electrolyte Mixtures Based on Ethylene Carbonate and Dimethyl Sulfone for Li-Ion Batteries with Improved Safety Characteristics.

    Science.gov (United States)

    Hofmann, Andreas; Migeot, Matthias; Thißen, Eva; Schulz, Michael; Heinzmann, Ralf; Indris, Sylvio; Bergfeldt, Thomas; Lei, Boxia; Ziebert, Carlos; Hanemann, Thomas

    2015-06-01

    In this study, novel electrolyte mixtures for Li-ion cells are presented with highly improved safety features. The electrolyte formulations are composed of ethylene carbonate/dimethyl sulfone (80:20 wt/wt) as the solvent mixture and LiBF4 , lithium bis(trifluoromethanesulfonyl)azanide, and lithium bis(oxalato)borate as the conducting salts. Initially, the electrolytes are characterized with regard to their physical properties, their lithium transport properties, and their electrochemical stability. The key advantages of the electrolytes are high flash points of >140 °C, which enhance significantly the intrinsic safety of Li-ion cells containing these electrolytes. This has been quantified by measurements in an accelerating rate calorimeter. By using the newly developed electrolytes, which are liquid down to T=-10 °C, it is possible to achieve C-rates of up to 1.5 C with >80 % of the initial specific capacity. During 100 cycles in cell tests (graphite||LiNi1/3 Co1/3 Mn1/3 O2 ), it is proven that the retention of the specific capacity is >98 % of the third discharge cycle with dependence on the conducting salt. The best electrolyte mixture yields a capacity retention of >96 % after 200 cycles in coin cells. PMID:25950145

  17. Poly(cyclohexadiene)-Based Polymer Electrolyte Membranes for Fuel Cell Applications

    Energy Technology Data Exchange (ETDEWEB)

    Mays, Jimmy W.

    2011-03-07

    The goal of this research project was to create and develop fuel cell membranes having high proton conductivity at high temperatures and high chemical and mechanical durability. Poly(1,3-cyclohexadiene) (PCHD) is of interest as an alternative polymer electrolyte membrane (PEM) material due to its ring-like structure which is expected to impart superior mechanical and thermal properties, and due to the fact that PCHD can readily be incorporated into a range of homopolymer and copolymer structures. PCHD can be aromatized, sulfonated, or fluorinated, allowing for tuning of key performance structure and properties. These factors include good proton transport, hydrophilicity, permeability (including fuel gas impermeability), good mechanical properties, morphology, thermal stability, crystallinity, and cost. The basic building block, 1,3-cyclohexadiene, is a hydrocarbon monomer that could be inexpensively produced on a commercial scale (pricing typical of other hydrocarbon monomers). Optimal material properties will result in novel low cost PEM membranes engineered for high conductivity at elevated temperatures and low relative humidities, as well as good performance and durability. The primary objectives of this project were: (1) To design, synthesize and characterize new non-Nafion PEM materials that conduct protons at low (25-50%) RH and at temperatures ranging from room temperature to 120 C; and (2) To achieve these objectives, a range of homopolymer and copolymer materials incorporating poly(cyclohexadiene) (PCHD) will be synthesized, derivatized, and characterized. These two objectives have been achieved. Sulfonated and crosslinked PCHD homopolymer membranes exhibit proton conductivities similar to Nafion in the mid-RH range, are superior to Nafion at higher RH, but are poorer than Nafion at RH < 50%. Thus to further improve proton conductivity, particularly at low RH, poly(ethylene glycol) (PEG) was incorporated into the membrane by blending and by

  18. Toward ambient temperature operation with all-solid-state lithium metal batteries with a sp3 boron-based solid single ion conducting polymer electrolyte

    Science.gov (United States)

    Zhang, Yunfeng; Cai, Weiwei; Rohan, Rupesh; Pan, Meize; Liu, Yuan; Liu, Xupo; Li, Cuicui; Sun, Yubao; Cheng, Hansong

    2016-02-01

    The ionic conductivity decay problem of poly(ethylene oxide) (PEO)-based solid polymer electrolytes (SPEs) when increase the lithium salt of the SPEs up to high concentration is here functionally overcome by the incorporation of a charge delocalized sp3 boron based single ion conducting polymer electrolyte (SIPE) with poly(ethylene oxide) to fabricate solid-state sp3 boron based SIPE membranes (S-BSMs). By characterizations, particularly differential scanning calorimeter (DSC) and ionic conductivity studies, the fabricated S-BSMs showed decreased melting points and increased ionic conductivity as steadily increase the content of sp3 boron based SIPE, which significantly improved the low temperature performance of the all-solid-state lithium batteries. The fabricated Li | S-BSMs | LiFePO4 cells exhibit highly electrochemical stability and excellent cycling at temperature below melting point of PEO, which has never been reported so far for SIPEs based all-solid-state lithium batteries.

  19. Ionic conductivity and transport properties of poly(vinylidene fluoride-co-hexafluoropropylene)-based solid polymer electrolytes

    Science.gov (United States)

    Abreha, Merhawi; Subrahmanyam, A. R.; Siva Kumar, J.

    2016-08-01

    Polymer electrolytes containing poly(vinylidene fluoride-co-hexafluoropropylene) (PVdF-HFP) and various concentrations of lithium triflate were prepared to determine the optimal polymer-salt composition for maximum ionic conductivity. Complex formation was ascertained from X-ray diffraction (XRD), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and differential scanning calorimetry (DSC) studies. The conductivity measurements reveal that the ionic conductivity of the polymer electrolytes containing various salt concentrations increases with temperature and obeys the Arrhenius rule. It is found that the electrolyte containing 25 wt.% of lithium triflate exhibits the highest room temperature conductivity. Moreover, Ionic transference measurements show predominance of ionic motion.

  20. Preparation of hybrid polymer based on polyurethane lithium salt and polyvinylidene fluoride as electrolyte for lithium-ion batteries

    International Nuclear Information System (INIS)

    Graphical abstract: The hybrid microporous membrane (PVDF/PLS-10) presents a uniform morphology and the corresponding HMGPE delivers high electrochemical stability and excellent cycleability. - Abstract: In this paper, hybrid microporous gel polymer electrolytes (HMGPEs) based onpolyvinylidene fluoride (PVdF)/polyurethane lithium salt (PLS) are fabricated by thermal phase separation technique. PLS is synthesized via condensation copolymerization of polyethylene glycol 800 (PEG800) and diphenyl-methane-diisocyanate(MDI), and then neutralized with LiOH. The effect of PLS on the morphologies of the hybrid membrane, electrochemical properties and cycle performance of the assembled polymer lithium-ion rechargeable batteries are studied in detail. The morphologies of the hybrid polymer membranes are examined by scanning electron microscope (SEM). The intercalation of PVdF/PLS hybrid membranes is characterized by X-ray diffraction (XRD), differential scanning calorimeter (DSC) and thermal gravimetric analysis (TGA). The incorporation of PLS in PVdF matrix can enhance ionic conductivities and electrochemical stabilities for the prepared HMGPEs. The assembled lithium-ion batteries based on HMGPEs with weight ratio 80:20 of PVdF and PLS (PVdF/PLS-20) delivers the highest charge-discharge capacity (about 175mAh g−1), and the cell based on HMGPEs of with weight ratio 90:10 of PVdF and PLS(PVdF/PLS-10) shows the best stability in cycle performance

  1. Low pressure carbon dioxide solubility in lithium-ion batteries based electrolytes as a function of temperature. Measurement and prediction

    International Nuclear Information System (INIS)

    Highlights: ► CO2 solubility is measured in pure alkylcarbonates and their binary mixtures. ► The CO2 solubility varies significantly for concentration LiPF6, LiTFSI and LiFAP salt. ► The dissolution of the CO2 in all solvents is entropy-driven and exothermic. ► CO2 solubilities were predicted using COSMOThermX and compared to measurements. -- Abstract: We present in this study the effect of nature and concentration of lithium salt, such as the lithium hexafluorophosphate, LiPF6; lithium tris(pentafluoroethane)-trifluorurophosphate LiFAP; lithium bis(trifluoromethylsulfonyl)imide, LiTFSI, on the CO2 solubility in four electrolytes for lithium ion batteries based on pure solvent that include ethylene carbonate (EC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC), as well as, in the EC:DMC, EC:EMC and EC:DEC (50:50) wt.% binary mixtures as a function of temperature from (283 to 353) K and atmospheric pressure. Based on experimental solubility values, the Henry’s law constant of the carbon dioxide in these solutions with the presence or absence of lithium salt was then deduced and compared with reported values from the literature, as well as with those predicted by using COSMO-RS methodology within COSMOThermX software. From this study, it appears that the addition of 1 mol · dm−3 LiPF6 salt in alkylcarbonate solvents decreases their CO2 capture capacity. By using the same experimental conditions, an opposite CO2 solubility trend was generally observed in the case of the addition of LiFAP or LiTFSI salts in these solutions. Additionally, in all solutions investigated during this work, the CO2 solubility is greater in electrolytes containing the LiFAP salt, followed by those based on the LiTFSI case. The precision and accuracy of the experimental data reported therein, which are close to (1 and 15)%, respectively. From the variation of the Henry’s law constant with temperature, the partial molar thermodynamic functions of

  2. Electrolytes for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Vaughey, John; Jansen, Andrew N.; Dees, Dennis W.

    2014-08-05

    A family of electrolytes for use in a lithium ion battery. The genus of electrolytes includes ketone-based solvents, such as, 2,4-dimethyl-3-pentanone; 3,3-dimethyl 2-butanone(pinacolone) and 2-butanone. These solvents can be used in combination with non-Lewis Acid salts, such as Li.sub.2[B.sub.12F.sub.12] and LiBOB.

  3. Polyacrylonitrile electrolytes. Part 1. A novel high-conductivity composite polymer electrolyte based on PAN, LiClO{sub 4} and {alpha}-Al{sub 2}O{sub 3}

    Energy Technology Data Exchange (ETDEWEB)

    Chen-Yang, Y.W.; Chen, H.C.; Lin, F.J.; Chen, C.C. [Department of Chemistry and Center for Nanotechnology at CYCU, Chung Yuan Christian University, 32023 Chung-Li (Taiwan, Province of China)

    2002-10-01

    In this work, a series of novel solid-type {alpha}-Al{sub 2}O{sub 3}-containing polyacrylonitrile (PAN)-based composite polymer electrolytes (CPE) with high conductivity and high mechanical property at room temperature has been prepared. The effect of the addition of {alpha}-Al{sub 2}O{sub 3} on the properties of the PAN-based composite polymer electrolyte has been analyzed. The best conductivities obtained at room temperature is 5.7x10{sup -4} S cm{sup -1} from the CPE with 7.5 wt.% {alpha}-Al{sub 2}O{sub 3} and 0.6 LiClO{sub 4} per PAN repeat unit. The stress-strain test result indicates that the membranes prepared possess high yield stress (73 kg cm{sup -2}) suitable for serving as separators in the solid-state lithium and lithium ion batteries and high yield elongation (225%) pliable to form good interface with electrodes. Also discussed are the effects of the addition of the ceramics on the interactions in the system and the possible conduction mechanism.

  4. Wireless capsule endoscopy video reduction based on camera motion estimation.

    Science.gov (United States)

    Liu, Hong; Pan, Ning; Lu, Heng; Song, Enmin; Wang, Qian; Hung, Chih-Cheng

    2013-04-01

    Wireless capsule endoscopy (WCE) is a novel technology aiming for investigating the diseases and abnormalities in small intestine. The major drawback of WCE examination is that it takes a long time to examine the whole WCE video. In this paper, we present a new reduction scheme for WCE video to reduce the examination time. To achieve this task, a WCE video motion model is proposed. Under this motion model, the WCE imaging motion is estimated in two stages (the coarse level and the fine level). In the coarse level, the WCE camera motion is estimated with a combination of Bee Algorithm and Mutual Information. In the fine level, the local gastrointestinal tract motion is estimated with SIFT flow. Based on the result of WCE imaging motion estimation, the reduction scheme preserves key images in WCE video with scene changes. From experimental results, we notice that the proposed motion model is suitable for the motion estimation in successive WCE images. Through the comparison with APRS and FCM-NMF scheme, our scheme can produce an acceptable reduction sequence for browsing and examination. PMID:22868484

  5. Suppression of Aluminum Corrosion in Lithium Bis(trifluoromethanesulfonyl)imide-based Electrolytes by the Addition of Fumed Silica

    Energy Technology Data Exchange (ETDEWEB)

    Louis, Hamenu; Ko, Jangmyoun [Hanbat National Univ., Daejeon (Korea, Republic of); Lee, Younggi; Kim, Kwangman [Electronics and Telecommunications Research Institute, Daejeon (Korea, Republic of); Cho, Wonil [Korea Institute of Science and Technology, Seoul (Korea, Republic of)

    2013-06-15

    The corrosion property of aluminum by lithium bis(trifluoromethanesulfonyl)imide (LiTFSI) salt is investigated in liquid and gel electrolytes consisting of ethylene carbonate/propylene carbonate/ethylmethyl carbonate/diethyl carbonate (20:5:55:20, vol %) with vinylene carbonate (2 wt %) and fluoroethylene carbonate (5 wt %) using conductivity measurement, cyclic voltammetry, scanning electron microscopy, and energy dispersive X-ray spectroscopy. All corrosion behaviors are attenuated remarkably by using three gel electrolytes containing 3 wt % of hydrophilic and hydrophobic fumed silica. The addition of silica particles contributes to the increase in the ionic conductivity of the electrolyte, indicating temporarily formed physical crosslinking among the silica particles to produce a gel state. Cyclic voltammetry also gives lower anodic current responses at higher potentials for repeating cycles, confirming further corrosion attenuation or electrochemical stability. In addition, the degree of corrosion attenuation can be affected mainly by the electrolytic constituents, not by the hydrophilicity or hydrophobicity of silica particles.

  6. Electrolytic phototransistor based on graphene-MoS2 van der Waals p-n heterojunction with tunable photoresponse

    Science.gov (United States)

    Henck, Hugo; Pierucci, Debora; Chaste, Julien; Naylor, Carl H.; Avila, Jose; Balan, Adrian; Silly, Mathieu G.; Asensio, Maria C.; Sirotti, Fausto; Johnson, A. T. Charlie; Lhuillier, Emmanuel; Ouerghi, Abdelkarim

    2016-09-01

    Van der Waals (vdW) heterostructures obtained by stacking 2D materials offer a promising route for next generation devices by combining different unique properties in completely new artificial materials. In particular, the vdW heterostructures combine high mobility and optical properties that can be exploited for optoelectronic devices. Since the p-n junction is one of the most fundamental units of optoelectronics, we propose an approach for its fabrication based on the intrinsic n doped MoS2 and the p doped bilayer graphene hybrid interfaces. We demonstrate the control of the photoconduction properties using electrolytic gating which ensures a low bias operation. We show that by finely choosing the doping value of each layer, the photoconductive properties of the hybrid system can be engineered to achieve magnitude and sign control of the photocurrent. Finally, we provide a simple phase diagram relating the photoconductive behavior with the chosen doping, which we believe can be very useful for the future design of the van der Waals based photodetectors.

  7. A urea biosensor based on pH-sensitive Sm2TiO5 electrolyte-insulator-semiconductor.

    Science.gov (United States)

    Pan, Tung-Ming; Huang, Ming-De; Lin, Wan-Ying; Wu, Min-Hsien

    2010-06-11

    A urea biosensor based on pH-sensitive Sm(2)TiO(5) electrolyte-insulator-semiconductor (EIS) has been described. We used X-ray diffraction, Auger electron spectroscopy, and atomic force microscopy to investigate the structural and morphological features of high-k Sm(2)TiO(5) sensing membranes that had been subjected to annealing at different temperatures. The EIS device incorporating a high-k Sm(2)TiO(5) sensing film that had been annealed at 900 degrees C exhibited good sensing characteristics, including a high sensitivity of 60.5 mV/pH (in solutions from pH 2 to 12), a small hysteresis voltage of 2.72 mV (in the pH loop 7-->4-->7-->10-->7), and a low drift rate of 1.15 mV h(-1) (in the buffer solution at pH 7). The Sm(2)TiO(5) EIS device also showed a high selective response towards H(+). This improvement can be attributed to the small number of crystal defects and the large surface roughness. In addition, the urea biosensor based on pH-sensitive EIS incorporating a Sm(2)TiO(5) sensing membrane annealed at 900 degrees C allowed the potentiometric analysis of urea, at concentrations ranging from 0.1 to 32 mM, with a sensitivity of 72.85 mV/purea.

  8. Solid Polymer Electrolytes Based on Functionalized Tannic Acids from Natural Resources for All-Solid-State Lithium-Ion Batteries.

    Science.gov (United States)

    Shim, Jimin; Bae, Ki Yoon; Kim, Hee Joong; Lee, Jin Hong; Kim, Dong-Gyun; Yoon, Woo Young; Lee, Jong-Chan

    2015-12-21

    Solid polymer electrolytes (SPEs) for all-solid-state lithium-ion batteries are prepared by simple one-pot polymerization induced by ultraviolet (UV) light using poly(ethylene glycol) methyl ether methacrylate (PEGMA) as an ion-conducting monomeric unit and tannic acid (TA)-based crosslinking agent and plasticizer. The crosslinking agent and plasticizer based on natural resources are obtained from the reaction of TA with glycidyl methacrylate and glycidyl poly(ethylene glycol), respectively. Dimensionally stable free-standing SPE having a large ionic conductivity of 5.6×10(-4)  Scm(-1) at room temperature can be obtained by the polymerization of PEGMA into P(PEGMA) with a very small amount (0.1 wt %) of the crosslinking agent and 2.0 wt % of the plasticizer. The ionic conductivity value of SPE with a crosslinked structure is one order of magnitude larger than that of linear P(PEGMA) in the waxy state.

  9. Electrochemical reduction approach-based 3D graphene/Ni(OH)2 electrode for high-performance supercapacitors

    International Nuclear Information System (INIS)

    Highlights: • 3D graphene foam is synthesized by a simple electrochemical reduction method. • The 3D graphene/Ni(OH)2 composite is used as a monolithic free-standing electrode material. • The 3D conductive graphene network improves the contact between electrode and electrolyte. • Compositing graphene with Ni(OH)2 sheets take full advantage of the synergistic effects. • Results show that the as-synthesized products have good electrochemical property. - Abstract: Using a simple electrochemical reduction approach, we have produced three-dimensional (3D) graphene foam having high conductivity and well-defined macroporous structure. Through a hydrothermal process, Ni(OH)2 sheets are grown in-situ onto the graphene surface. This monolithic 3D graphene/Ni(OH)2 composite is used as the free-standing electrode for supercapacitor application; it shows a high specific capacitance of 183.1 F g−1 (based on the total mass of the electrode), along with excellent rate capability and cycle performance. The asymmetric supercapacitor based on the 3D graphene/Ni(OH)2 as a positive electrode and active carbon (AC) as a negative electrode is also assembled and it exhibits a specific capacitance of 148.3 F g−1 at 0.56 A g−1 and a high energy density of 52.7 W h kg−1 at a power density of 444.4 W kg−1. Moreover, 3D graphene/Ni(OH)2//AC has a good cycle stability (87.9% capacitance retention after 1000 cycles), making it promising as one of the most attractive candidates for electrochemical energy storage. This excellent electrochemical performance results from the multiplexed 3D graphene network facilitating electron transport; the interlaced Ni(OH)2 sheets shorten ion diffusion paths and facilitate the rapid migration of electrolyte ions

  10. Identification of Diethyl 2,5-Dioxahexane Dicarboxylate and Polyethylene Carbonate as Decomposition Products of Ethylene Carbonate Based Electrolytes by Fourier Transform Infrared Spectroscopy

    KAUST Repository

    Shi, Feifei

    2014-07-10

    The formation of passive films on electrodes due to electrolyte decomposition significantly affects the reversibility of Li-ion batteries (LIBs); however, understanding of the electrolyte decomposition process is still lacking. The decomposition products of ethylene carbonate (EC)-based electrolytes on Sn and Ni electrodes are investigated in this study by Fourier transform infrared (FTIR) spectroscopy. The reference compounds, diethyl 2,5-dioxahexane dicarboxylate (DEDOHC) and polyethylene carbonate (poly-EC), were synthesized, and their chemical structures were characterized by FTIR spectroscopy and nuclear magnetic resonance (NMR). Assignment of the vibration frequencies of these compounds was assisted by quantum chemical (Hartree-Fock) calculations. The effect of Li-ion solvation on the FTIR spectra was studied by introducing the synthesized reference compounds into the electrolyte. EC decomposition products formed on Sn and Ni electrodes were identified as DEDOHC and poly-EC by matching the features of surface species formed on the electrodes with reference spectra. The results of this study demonstrate the importance of accounting for the solvation effect in FTIR analysis of the decomposition products forming on LIB electrodes. © 2014 American Chemical Society.

  11. Novel electrolyte mixtures based on dimethyl sulfone, ethylene carbonate and LiPF6 for lithium-ion batteries

    Science.gov (United States)

    Hofmann, Andreas; Hanemann, Thomas

    2015-12-01

    In this study, novel electrolyte mixtures for Li-ion cells are presented which are composed of ethylene carbonate/dimethyl sulfone (80:20 wt./wt.) as a solvent mixture and LiPF6, lithium bis(oxalato)borate and lithium difluoro(oxalato)borate as conducting salts. The main advantages of the solvent mixture are high flash points of >140 °C which enhance the intrinsic safety of Li-ion cells while maintaining good cell performance above 0-5 °C. The movability of the lithium ions in the electrolyte is investigated via programmed current derivative chronopotentiometry. It is found that pure electrolyte properties cannot necessarily predict the electrolyte behavior in real Li-ion cells but the complex interplay between electrolytes, electrode materials and separators has to be taken into account. Using the newly developed electrolytes, it is possible to achieve C-rates up to 1.5C with >80% of the initial specific discharge capacity (25 °C). Within 200 cycles during one month in cell tests (C||NMC) it is proven that the retention of the specific capacity is >98% of the third discharge cycle in dependence of the conducting salt.

  12. Dual phase polymer gel electrolyte based on non-woven poly(vinylidenefluoride-co-hexafluoropropylene)–layered clay nanocomposite fibrous membranes for lithium ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Shubha, Nageswaran [School of Materials Science and Engineering, Nanyang Technological University, Block N4.1, 50 Nanyang Avenue, Singapore 639798 (Singapore); Prasanth, Raghavan [School of Materials Science and Engineering, Nanyang Technological University, Block N4.1, 50 Nanyang Avenue, Singapore 639798 (Singapore); Energy Research Institute - NTU (ERI-N) Research Techno Plaza, 50 Nanyang Drive, Singapore 637553 (Singapore); TUM-CREATE Center for Electromobility, Nanyang Technological University, Singapore 637553 (Singapore); Hoon, Hng Huey [School of Materials Science and Engineering, Nanyang Technological University, Block N4.1, 50 Nanyang Avenue, Singapore 639798 (Singapore); Srinivasan, Madhavi, E-mail: madhavi@ntu.edu.sg [School of Materials Science and Engineering, Nanyang Technological University, Block N4.1, 50 Nanyang Avenue, Singapore 639798 (Singapore); Energy Research Institute - NTU (ERI-N) Research Techno Plaza, 50 Nanyang Drive, Singapore 637553 (Singapore); TUM-CREATE Center for Electromobility, Nanyang Technological University, Singapore 637553 (Singapore)

    2013-02-15

    Graphical abstract: Display Omitted Highlights: ► P(VdF-co-HFP)–clay nanocomposite based electrospun membranes are prepared. ► The membranes are used as polymer gel electrolyte (PGE) in lithium ion batteries. ► The composite PGE shows ionic conductivity of 5.5 mS cm{sup −1} at room temperature. ► Li/PGE/LiFePO{sub 4} cell delivers initial discharge capacity of 160 mAh g{sup −1}. ► The use of prepared electrolyte significantly improved the cell performance. -- Abstract: A new approach for fabricating polymer gel electrolytes (PGEs) based on electrospun poly(vinylidenefluoride-co-hexafluoropropylene) (P(VdF-co-HFP)) incorporated with layered nanoclay has been employed to enhance the ionic conductivity and electrochemical properties of P(VdF-co-HFP) without compromising its mechanical strength. The effect of layered nanoclay on properties of membranes has been evaluated by X-ray diffraction (XRD), differential scanning calorimetry (DSC) and thermal gravimetric analysis (TGA). Surface morphology of the membranes has been studied using field-emission scanning electron microscopy (FE-SEM). Polymer gel electrolytes are prepared by soaking the fibrous membrane into 1 M LiPF{sub 6} in EC/DEC. The electrochemical studies show that incorporation of layered nanoclay into the polymer matrix greatly enhanced the ionic conductivity and compatibility with lithium electrodes. The charge–discharge properties and cycling performance of Li/LiFePO{sub 4} cells comprising nanocomposite polymer gel electrolytes have been evaluated at room temperature.

  13. Reduction of inequalities in health: assessing evidence-based tools

    Directory of Open Access Journals (Sweden)

    Shea Beverley

    2006-09-01

    Full Text Available Abstract Background The reduction of health inequalities is a focus of many national and international health organisations. The need for pragmatic evidence-based approaches has led to the development of a number of evidence-based equity initiatives. This paper describes a new program that focuses upon evidence- based tools, which are useful for policy initiatives that reduce inequities. Methods This paper is based on a presentation that was given at the "Regional Consultation on Policy Tools: Equity in Population Health Reports," held in Toronto, Canada in June 2002. Results Five assessment tools were presented. 1. A database of systematic reviews on the effects of educational, legal, social, and health interventions to reduce unfair inequalities is being established through the Cochrane and Campbell Collaborations. 2 Decision aids and shared decision making can be facilitated in disadvantaged groups by 'health coaches' to help people become better decision makers, negotiators, and navigators of the health system; a pilot study in Chile has provided proof of this concept. 3. The CIET Cycle: Combining adapted cluster survey techniques with qualitative methods, CIET's population based applications support evidence-based decision making at local and national levels. The CIET map generates maps directly from survey or routine institutional data, to be used as evidence-based decisions aids. Complex data can be displayed attractively, providing an important tool for studying and comparing health indicators among and between different populations. 4. The Ottawa Equity Gauge is applying the Global Equity Gauge Alliance framework to an industrialised country setting. 5 The Needs-Based Health Assessment Toolkit, established to assemble information on which clinical and health policy decisions can be based, is being expanded to ensure a focus on distribution and average health indicators. Conclusion Evidence-based planning tools have much to offer the

  14. Speckle reduction by phase-based weighted least squares.

    Science.gov (United States)

    Zhu, Lei; Wang, Weiming; Qin, Jing; Heng, Pheng-Ann

    2014-01-01

    Although ultrasonography has been widely used in clinical applications, the doctor suffers great difficulties in diagnosis due to the artifacts of ultrasound images, especially the speckle noise. This paper proposes a novel framework for speckle reduction by using a phase-based weighted least squares optimization. The proposed approach can effectively smooth out speckle noise while preserving the features in the image, e.g., edges with different contrasts. To this end, we first employ a local phase-based measure, which is theoretically intensity-invariant, to extract the edge map from the input image. The edge map is then incorporated into the weighted least squares framework to supervise the optimization during despeckling, so that low contrast edges can be retained while the noise has been greatly removed. Experimental results in synthetic and clinical ultrasound images demonstrate that our approach performs better than state-of-the-art methods. PMID:25570846

  15. Effects of TiO{sub 2} addition on ionic conductivity of PVC/PEMA blend based composite polymer electrolyte

    Energy Technology Data Exchange (ETDEWEB)

    Subban, R. H. Y. [Institute of Science Universiti Teknologi MARA 40450 Shah Alam Selangor Malaysia (Malaysia); Facultyof Applied Sciences Universiti Teknologi MARA40450 Shah Alam Selangor Malaysia (Malaysia); Sukri, Nursyazwani [Facultyof Applied Sciences Universiti Teknologi MARA40450 Shah Alam Selangor Malaysia (Malaysia)

    2015-08-28

    PVC/PEMA blend based polymer electrolytes with lithium bistrifluoromethane sulfonimide (LiN(CF{sub 3}SO{sub 2}){sub 2}) and PVC/PEMA/(LiN(CF{sub 3}SO{sub 2}){sub 2}-TiO{sub 2} films were prepared by solution cast technique. The sample containing 35 wt. % LiN(CF{sub 3}SO{sub 2}){sub 2} exhibited the highest conductivity of 1.75 × 10{sup −5} Scm{sup −1}. The conductivity of the sample increased to 2.12 × 10{sup −5} Scm{sup −1} and 4.61 × 10{sup −5} Scm{sup −1} when 4 wt. % and 10 wt. % of titanium dioxide (TiO{sub 2}) was added to the sample at 65 wt. % PVC/PEMA-35 wt. % LiN(CF{sub 3}SO{sub 2}){sub 2} composition respectively. The low increase in conductivity is attributed to two competing factors: increase in crystallinity as accounted by X-Ray diffraction (XRD) and decrease in glass transition temperature as accounted by differential scanning calorimetry (DSC)

  16. Structure and properties of solid polymer electrolyte based on chitosan and ZrO2 nanoparticle for lithium ion battery

    Science.gov (United States)

    Sudaryanto, Yulianti, Evi; Patimatuzzohrah

    2016-02-01

    In order to develop all solid lithium ion battery, study on the structure and properties of solid polymer electrolytes (SPE) based on chitosan has been done. The SPE were prepared by adding Zirconia (ZrO2) nanoparticle and LiClO4 as lithium salt into the chitosan solution followed by casting method. Effect of the ZrO2 and salt concentration to the structure and properties of SPE were elaborated using several methods. The structure of the SPE cast film, were characterized mainly by using X-ray diffractometer (XRD). While the electrical properties of SPE were studied by electrochemical impedance spectrometer (EIS) and ion transference number measurement. XRD profiles show that the addition of ZrO2 and LiClO4 disrupts the crystality of chitosan. The decrease in sample crytalinity with the nanoparticle and salt addition may increase the molecular mobility result in the increasing sample conductivity and cathionic transference number as determined by EIS and ion transference number measurement, respectively. The highest ionic conductivity (3.58×10-4 S cm-1) was obtained when 4 wt% of ZrO2 nanoparticle and 40 wt% of LiClO4 salt were added to the chitosan. The ion transference number with that composition was 0.55. It is high enough to be used as SPE for lithium ion battery.

  17. Electrodeposition of In{sub 2}O{sub 3} thin films from a dimethylsulfoxide based electrolytic solution

    Energy Technology Data Exchange (ETDEWEB)

    Henriquez, R.; Munoz, E.; Gomez, H. [Instituto de Quimica, Facultad de Ciencias, Pontificia Universidad Catolica de Valparaiso, Curauma Valparaiso (Chile); Dalchiele, E.A.; Marotti, R.E. [Instituto de Fisica and CINQUIFIMA, Facultad de Ingenieria, Montevideo (Uruguay); Martin, F.; Leinen, D.; Ramos-Barrado, J.R. [Laboratorio de Materiales y Superficie, Departamento de Fisica Aplicada and Ingenieria Quimica, Universidad de Malaga (Spain)

    2013-02-15

    Indium (III) oxide (In{sub 2}O{sub 3}) thin films have been obtained after heat treatment of In(OH){sub 3} precursor layers grown by a potential cycling electrodeposition (PCED) method from a dimethylsulfoxide (DMSO) based electrolytic solution onto fluorine-doped tin oxide (FTO) coated glass substrates. X-ray diffraction (XRD) measurements indicate the formation of a polycrystalline In{sub 2}O{sub 3} phase with a cubic structure. Scanning electron microscopy (SEM) and atomic force microscopy (AFM) showed a smooth morphology of the In{sub 2}O{sub 3} thin films after an optimized heat treatment had been developed. The surface composition and chemical state of the semiconductor films was established by X-ray photoelectron spectroscopy analysis. The nature of the semiconductor material, flat band potential and donor density were determined from Mott-Schottky plots. This study reveals that the In{sub 2}O{sub 3} films exhibited n-type conductivity with an average donor density of 2.2 x 10{sup 17} cm{sup -3}. The optical characteristics were determined through transmittance spectra. The direct and indirect band gap values obtained are according to the accepted values for the In{sub 2}O{sub 3} films of 2.83 and 3.54 eV for the indirect and direct band gap values. (Copyright copyright 2013 WILEY-VCH Verlag GmbH and Co. KGaA, Weinheim)

  18. Effects of TiO2 addition on ionic conductivity of PVC/PEMA blend based composite polymer electrolyte

    International Nuclear Information System (INIS)

    PVC/PEMA blend based polymer electrolytes with lithium bistrifluoromethane sulfonimide (LiN(CF3SO2)2) and PVC/PEMA/(LiN(CF3SO2)2-TiO2 films were prepared by solution cast technique. The sample containing 35 wt. % LiN(CF3SO2)2 exhibited the highest conductivity of 1.75 × 10−5 Scm−1. The conductivity of the sample increased to 2.12 × 10−5 Scm−1 and 4.61 × 10−5 Scm−1 when 4 wt. % and 10 wt. % of titanium dioxide (TiO2) was added to the sample at 65 wt. % PVC/PEMA-35 wt. % LiN(CF3SO2)2 composition respectively. The low increase in conductivity is attributed to two competing factors: increase in crystallinity as accounted by X-Ray diffraction (XRD) and decrease in glass transition temperature as accounted by differential scanning calorimetry (DSC)

  19. Steam Electrolysis by Proton-Conducting Solid Oxide Electrolysis Cells (SOECs) with Chemically Stable BaZrO3-Based Electrolytes

    KAUST Repository

    Bi, Lei

    2015-07-17

    BaZrO3-based material was applied as the electrolyte for proton-conducting solid oxide fuel cells (SOECs). Compared with the instability of BaCeO3-based proton-conductors, BaZrO3-based material could be a more promising candidate for proton-conducting SOECs due to its excellent chemical stability under H2O conditions, but few reports on this aspect has been made due to the processing difficulty for BaZrO3. Our recent pioneering work has demonstrated the feasibility of using BaZrO3-based electrolyte for SOECs and the fabricated cell achieves relatively high cell performance, which is comparable or even higher than that for BaCeO3-based SOECs and offers better chemical stability. Cell performance can be further improved by tailoring the electrolyte and electrode. © The Electrochemical Society.

  20. Flow velocimetry for weakly conducting electrolytes based on high resolution Lorentz force measurement.

    Science.gov (United States)

    Resagk, Christian; Ebert, Reschad; Vasilyan, Suren; Wiederhold, Andreas

    2013-11-01

    We demonstrate that a flow velocity measurement can be transformed into a non-invasive force measurement by metering the drag force acting on a system of magnets around a flow channel. This method is called Lorentz force velocimetry and has been developed in the last years in our institute. It is a feasible principle for materials with large conductivity like liquid metals. To evolve this method for weakly conducting fluids like salt water or molten glass the drag force measurement is the challenging bottleneck. Here forces of 10-8 and less of the weight force of the magnet system have to be resolved. In this paper different force measurement techniques get tested and compared. For the current setup the magnet system is attached to a state of the art electromagnetic force compensation balance. Different ways of getting the correct force signal out of the two measurement setups will be presented and discussed. For generalization of the measurement principle the Lorentz force is determined for different fluid profiles. In addition to that we have developed new systematic noise reduction methods to increase the resolution of the force measurement techniques by a factor of ten or larger which we will present here.

  1. Significant Performance Enhancement in Asymmetric Supercapacitors based on Metal Oxides, Carbon nanotubes and Neutral Aqueous Electrolyte

    OpenAIRE

    Arvinder Singh; Amreesh Chandra

    2015-01-01

    Amongst the materials being investigated for supercapacitor electrodes, carbon based materials are most investigated. However, pure carbon materials suffer from inherent physical processes which limit the maximum specific energy and power that can be achieved in an energy storage device. Therefore, use of carbon-based composites with suitable nano-materials is attaining prominence. The synergistic effect between the pseudocapacitive nanomaterials (high specific energy) and carbon (high specif...

  2. Factors influencing high voltage performance of coconut char derived carbon based electrical double layer capacitor made using acetonitrile and propylene carbonate based electrolytes

    Science.gov (United States)

    Hu, Changzheng; Qu, Weiguo; Rajagopalan, Ramakrishnan; Randall, Clive

    2014-12-01

    Symmetric EDLCs made using high purity carbon electrodes derived from coconut char were tested using 1 M Tetraethylammonium hexafluorophosphate dissolved in two different solvents namely acetonitrile and propylene carbonate. The cell voltage of the capacitor made using propylene carbonate can be extended to 3.5 V and it exhibited good cycling and thermal stability upto 70 °C while the voltage was limited to below 3.0 V in acetonitrile. XPS analysis of the positive and negative electrodes of EDLCs post cycling showed that the primary degradation products were related to ring opening reactions in propylene carbonate based electrolytes while water played a key role in degradation of acetonitrile based EDLCs.

  3. Oxygen reduction by lithiated graphene and graphene-based materials.

    Science.gov (United States)

    Kataev, Elmar Yu; Itkis, Daniil M; Fedorov, Alexander V; Senkovsky, Boris V; Usachov, Dmitry Yu; Verbitskiy, Nikolay I; Grüneis, Alexander; Barinov, Alexei; Tsukanova, Daria Yu; Volykhov, Andrey A; Mironovich, Kirill V; Krivchenko, Victor A; Rybin, Maksim G; Obraztsova, Elena D; Laubschat, Clemens; Vyalikh, Denis V; Yashina, Lada V

    2015-01-27

    Oxygen reduction reaction (ORR) plays a key role in lithium-air batteries (LABs) that attract great attention thanks to their high theoretical specific energy several times exceeding that of lithium-ion batteries. Because of their high surface area, high electric conductivity, and low specific weight, various carbons are often materials of choice for applications as the LAB cathode. Unfortunately, the possibility of practical application of such batteries is still under question as the sustainable operation of LABs with carbon cathodes is not demonstrated yet and the cyclability is quite poor, which is usually associated with oxygen reduced species side reactions. However, the mechanisms of carbon reactivity toward these species are still unclear. Here, we report a direct in situ X-ray photoelectron spectroscopy study of oxygen reduction by lithiated graphene and graphene-based materials. Although lithium peroxide (Li2O2) and lithium oxide (Li2O) reactions with carbon are thermodynamically favorable, neither of them was found to react even at elevated temperatures. As lithium superoxide is not stable at room temperature, potassium superoxide (KO2) prepared in situ was used instead to test the reactivity of graphene with superoxide species. In contrast to Li2O2 and Li2O, KO2 was demonstrated to be strongly reactive.

  4. Fluorinated Alkoxide-Based Magnesium-Ion Battery Electrolytes that Demonstrate Li-Ion-Battery-Like High Anodic Stability and Solution Conductivity.

    Science.gov (United States)

    Crowe, Adam J; Stringham, Kyle K; Bartlett, Bart M

    2016-09-01

    Based on DFT predictions, a series of highly soluble fluorinated alkoxide-based electrolytes were prepared, examined electrochemically, and reversibly cycled. The alcohols react with ethylmagnesium chloride to generate a fluoroalkoxy-magnesium chloride intermediate, which subsequently reacts with aluminum chloride to generate the electrolyte. Solutions starting from a 1,1,1,3,3,3-hexafluoro-2-methylpropan-2-ol precursor exhibit high anodic stability, 3.2 V vs Mg(2+/0), and a record 3.5 mS/cm solution conductivity. Excellent galvanostatic cycling and capacity retention (94%) is observed with more than 300 h of cycle time while employing the standard Chevrel phase-Mo6S8 cathode material.

  5. Low pressure methane solubility in lithium-ion batteries based solvents and electrolytes as a function of temperature. Measurement and prediction

    International Nuclear Information System (INIS)

    Highlights: • CH4 solubility is measured in pure alkylcarbonates and their binary mixtures. • The CH4 solubility increases in the following order: EC < PC < DMC < EMC < DEC. • The dissolution of the CH4 in all systems was compared to the CO2 solubility. • CH4 solubility was predicted using COSMOthermX and compared to measurements. - Abstract: The methane solubility in five pure electrolyte solvents and one binary solvent mixture for lithium ion batteries – such as ethylene carbonate (EC), propylene carbonate (PC), dimethyl carbonate (DMC), ethyl methyl carbonate (EMC), diethyl carbonate (DEC) and the (50:50 wt%) mixture of EC:DMC was studied experimentally at pressures close to atmospheric and as a function of temperature between (280 and 343) K by using an isochoric saturation technique. The effect of the selected anions of a lithium salt LiX (X = hexafluorophosphate, PF6-; tris(pentafluoroethane)trifluorurophosphate, FAP−; bis(trifluoromethylsulfonyl)imide, TFSI−) on the methane solubility in electrolytes for lithium ion batteries was then investigated using a model electrolyte based on the binary mixture of EC:DMC (50:50 wt%) + 1 mol · dm−3 of lithium salt in the same temperature and pressure ranges. Based on experimental solubility data, the Henry’s law constant of the methane in these solutions were then deduced and compared together and with those predicted by using COSMO-RS methodology within COSMOthermX software. From this study, it appears that the methane solubility in each pure solvent decreases with the temperature and increases in the following order: EC < PC < EC:EMC (50:50 wt%) < DMC < EMC < DEC, showing that this increases with the van der Walls force in solution. Additionally, in all investigated EC:DMC (50:50 wt%) + 1 mol · dm−3 of lithium salt electrolytes, the methane solubility decreases also with the temperature and the methane solubility is higher in the electrolyte containing the LiFAP salt, followed by that based on

  6. Novel Electrolytes for Lithium Ion Batteries

    Energy Technology Data Exchange (ETDEWEB)

    Lucht, Brett L

    2014-12-12

    We have been investigating three primary areas related to lithium ion battery electrolytes. First, we have been investigating the thermal stability of novel electrolytes for lithium ion batteries, in particular borate based salts. Second, we have been investigating novel additives to improve the calendar life of lithium ion batteries. Third, we have been investigating the thermal decomposition reactions of electrolytes for lithium-oxygen batteries.

  7. Direct Electrical Detection of DNA Hybridization Based on Electrolyte-Gated Graphene Field-Effect Transistor

    Science.gov (United States)

    Ohno, Yasuhide; Okamoto, Shogo; Maehashi, Kenzo; Matsumoto, Kazuhiko

    2013-11-01

    DNA hybridization was electrically detected by graphene field-effect transistors. Probe DNA was modified on the graphene channel by a pyrene-based linker material. The transfer characteristic was shifted by the negative charges on the probe DNA, and the drain current was changed by the full-complementary DNA while no current change was observed after adding noncomplementary DNA, indicating that the graphene field-effect transistor detected the DNA hybridization. In addition, the number of DNAs was estimated by the simple plate capacitor model. As a result, one probe DNA was attached on the graphene channel per 10×10 nm2, indicating their high density functionalization. We estimated that 30% of probe DNA on the graphene channel was hybridized with 200 nM full-complementary DNA while only 5% of probe DNA was bound to the noncomplementary DNA. These results will help to pave the way for future biosensing applications based on graphene FETs.

  8. Spectrophotometric total reducing sugars assay based on cupric reduction.

    Science.gov (United States)

    Başkan, Kevser Sözgen; Tütem, Esma; Akyüz, Esin; Özen, Seda; Apak, Reşat

    2016-01-15

    As the concentration of reducing sugars (RS) is controlled by European legislation for certain specific food and beverages, a simple and sensitive spectrophotometric method for the determination of RS in various food products is proposed. The method is based on the reduction of Cu(II) to Cu(I) with reducing sugars in alkaline medium in the presence of 2,9-dimethyl-1,10-phenanthroline (neocuproine: Nc), followed by the formation of a colored Cu(I)-Nc charge-transfer complex. All simple sugars tested had the linear regression equations with almost equal slope values. The proposed method was successfully applied to fresh apple juice, commercial fruit juices, milk, honey and onion juice. Interference effect of phenolic compounds in plant samples was eliminated by a solid phase extraction (SPE) clean-up process. The method was proven to have higher sensitivity and precision than the widely used dinitrosalicylic acid (DNS) colorimetric method.

  9. Dimensionality Reduction using SOM based Technique for Face Recognition

    Directory of Open Access Journals (Sweden)

    Dinesh Kumar

    2008-05-01

    Full Text Available Unsupervised or Self-Organized learning algorithms have become very popular for discovery of significant patterns or features in the input data. The three prominent algorithms namely Principal Component Analysis (PCA, Self Organizing Maps (SOM, and Independent Component Analysis (ICA have widely and successfully been used for face recognition. In this paper a SOM based technique for dimensionality reduction has been proposed. This technique has also been successfully used for face recognition. A comparative study of PCA, SOM and ICA along with the proposed technique for face recognition has also been given. Simulation results indicate that SOM is better than the other techniques for the given face database and the classifier used. The results also show that the performance of the system decreases as the number of classes increase.

  10. Spectrophotometric total reducing sugars assay based on cupric reduction.

    Science.gov (United States)

    Başkan, Kevser Sözgen; Tütem, Esma; Akyüz, Esin; Özen, Seda; Apak, Reşat

    2016-01-15

    As the concentration of reducing sugars (RS) is controlled by European legislation for certain specific food and beverages, a simple and sensitive spectrophotometric method for the determination of RS in various food products is proposed. The method is based on the reduction of Cu(II) to Cu(I) with reducing sugars in alkaline medium in the presence of 2,9-dimethyl-1,10-phenanthroline (neocuproine: Nc), followed by the formation of a colored Cu(I)-Nc charge-transfer complex. All simple sugars tested had the linear regression equations with almost equal slope values. The proposed method was successfully applied to fresh apple juice, commercial fruit juices, milk, honey and onion juice. Interference effect of phenolic compounds in plant samples was eliminated by a solid phase extraction (SPE) clean-up process. The method was proven to have higher sensitivity and precision than the widely used dinitrosalicylic acid (DNS) colorimetric method. PMID:26592591

  11. Ionic conductivity and electrochemical properties of nanocomposite polymer electrolytes based on electrospun poly(vinylidene fluoride-co-hexafluoropropylene) with nano-sized ceramic fillers

    International Nuclear Information System (INIS)

    A series of nanocomposite polymer electrolytes (NCPEs) comprising nanoparticles of BaTiO3, Al2O3 or SiO2 were prepared by electrospinning technique. The nano-sized ceramic fillers were incorporated into poly(vinylidene fluoride-co-hexafluoropropylene) [P(VdF-HEP)] membranes during the electrospinning process. The resultant porous membranes are good absorbent of the liquid electrolyte and exhibit high electrolyte retention capacity. The presence of the ceramic nanoparticles has positive effect on the mechanical properties of the membranes. The ionic conductivity and the electrochemical stability window of the electrospun P(VdF-HFP)-based polymer are enhanced by the presence of the fillers. The cell Li/LiFePO4 based on the NCPE containing BaTiO3 delivers a discharge capacity of 164 mAh/g, which corresponds to 96.5% utilization of the active material. In comparison, the performance of Li/LiFePO4 cells with NCPEs containing Al2O3 and SiO2 was observed to be lower with respective discharge capacities of 153 and 156 mAh/g. The enhanced performance of the BaTiO3-based-NCPE is attributed mainly to its better interaction with the host polymer and compatibility with lithium metal

  12. Effect of nanosized silica in poly(methyl methacrylate)-lithium bis(trifluoromethanesulfonyl)imide based polymer electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Ramesh, S.; Lu, Soon-Chien [Faculty of Engineering and Science, Universiti Tunku Abdul Rahman, Setapak, 53300 Kuala Lumpur (Malaysia)

    2008-12-01

    The effect of nanosized silica when incorporated in polymer electrolytes is analyzed by means of Fourier transform infrared (FTIR) spectroscopy, conductivity and thermal properties. Nanocomposite polymer electrolytes are synthesized by the dispersion of nanosized silica (SiO{sub 2}), up to 10 wt.% maximum, into a matrix formed by poly(methyl methacrylate) (PMMA) and lithium bis(trifluoromethanesulfonyl)imide (LiTFSI). The highest conductivity is 2.44 x 10{sup -6} S cm{sup -1} at room temperature, with 4 wt.% of silica added. The FTIR spectra show evidence of complexation between PMMA, LiTFSI and SiO{sub 2}. The addition of silica to the polymer electrolytes also improves the thermal stability and the ability to retain conductivity over time. (author)

  13. Capacitively coupled electrolyte-conductivity sensor based on high-k material of barium strontium titanate

    OpenAIRE

    Huck, C.; Poghossian, A; Baecker, M; Chaudhuri, S.; Zander, W; Schubert, J.; Begoyan, V. K.; Buniatyan, V. V.; Wagner, Patrick Hermann; Schoening, M. J

    2014-01-01

    A miniaturized capacitively coupled contactless conductivity detection (C4D) sensor based on high-kperovskite oxide of barium strontium titanate (BST) has been implemented for the first time. The BST films(∼120 nm thick) of Ba0.25Sr0.75TiO3composition were prepared on a p-Si-SiO2-Pt structure by pulsed laserdeposition technique using BST targets fabricated by the self-propagating high-temperature synthesismethod. The Pt electrodes were buried into the SiO2layer to obtain a planar structure. F...

  14. Fuel cells with solid polymer electrolyte and their application on vehicles

    Energy Technology Data Exchange (ETDEWEB)

    Fateev, V.

    1996-04-01

    In Russia, solid polymer electrolyte MF-4-SK has been developed for fuel cells. This electrolyte is based on perfluorinated polymer with functional sulfogroups. Investigations on electrolyte properties and electrocatalysts have been carried out.

  15. FPGA based algorithms for data reduction at Belle II

    Energy Technology Data Exchange (ETDEWEB)

    Muenchow, David; Gessler, Thomas; Kuehn, Wolfgang; Lange, Jens Soeren; Liu, Ming; Spruck, Bjoern [II. Physikalisches Institut, Universitaet Giessen (Germany)

    2011-07-01

    Belle II, the upgrade of the existing Belle experiment at Super-KEKB in Tsukuba, Japan, is an asymmetric e{sup +}e{sup -} collider with a design luminosity of 8.10{sup 35}cm{sup -2}s{sup -1}. At Belle II the estimated event rate is {<=}30 kHz. The resulting data rate at the Pixel Detector (PXD) will be {<=}7.2 GB/s. This data rate needs to be reduced to be able to process and store the data. A region of interest (ROI) selection is based upon two mechanisms. a.) a tracklet finder using the silicon strip detector and b.) the HLT using all other Belle II subdetectors. These ROIs and the pixel data are forwarded to an FPGA based Compute Node for processing. Here a VHDL based algorithm on FPGA with the benefit of pipelining and parallelisation will be implemented. For a fast data handling we developed a dedicated memory management system for buffering and storing the data. The status of the implementation and performance tests of the memory manager and data reduction algorithm is presented.

  16. Noise Reduction for a MEMS-Gyroscope-Based Head Mouse.

    Science.gov (United States)

    Du, Jiaying; Gerdtman, Christer; Lindén, Maria

    2015-01-01

    In this paper, four different signal processing algorithms which can be applied to reduce the noise from a MEMS-gyroscope-based computer head mouse are presented. MEMS-gyroscopes are small, light, cheap and widely used in many electrical products. MultiPos, a MEMS-gyroscope-based computer head mouse system was designed for persons with movement disorders. Noise such as physiological tremor and electrical noise is a common problem for the MultiPos system. In this study four different signal processing algorithms were applied and evaluated by simulation in MATLAB and implementation in a dsPIC, with aim to minimize the noise in MultiPos. The algorithms were low-pass filter, Least Mean Square (LMS) algorithm, Kalman filter and Weighted Fourier Linear Combiner (WFLC) algorithm. Comparisons and system tests show that these signal processing algorithms can be used to improve the MultiPos system. The WFLC algorithm was found the best method for noise reduction in the application of a MEMS-gyroscope-based head mouse.

  17. CASCADED MULTILEVEL INVERTER BASED HARMONIC REDUCTION IN STATCOM

    Directory of Open Access Journals (Sweden)

    T. MANOKARAN,

    2010-10-01

    Full Text Available This paper deals with simulation of STATCOM used for harmonic reduction with the help of multilevel VSI circuit. Cascaded converter based multilevel inverters are used for medium to high power reactivecompensation application. Voltage unbalance is one of the main limitations of cascaded based multilevel STATCOM. A simple control strategy is proposed for the volt-age balance of a cascaded two level inverter based STATCOM. The topology consists of two conventional three phase two level inverters connected in cascade. The two inverters operate at two different dc link voltages to obtain four level operation at STATCOM out-put. Simulation studies are carried out to predict the performance of the proposed control strategy.The harmonics in STATCOM due to the voltage ripple are reduced. As a result, the size of inductor and DC capacitor can be reduced. The STATCOM has the great advantage of a fewer number of devices. The VSI is extremely fast in response to reactive power change. The simulation of the STATCOM is performed in the Simulink environment and the results are presented.

  18. Initial study of Nickel Electrolyte for EnFACE Process

    Directory of Open Access Journals (Sweden)

    Tri Widayatno

    2015-03-01

    Full Text Available Nickel electrolyte for a micro-pattern transfer process without photolithography, EnFACE, has been developed. Previous work on copper deposition indicated that a conductivity of ~2.7 Sm-1 is required. Electrochemical parameters of electrolyte i.e. current density and overpotential are also crucial to govern a successful pattern replication. Therefore, the investigation focused on the measurement of physicochemical properties and electrochemical behaviour of the electrolyte at different nickel concentrations and complexing agents of chloride and sulfamate. Nickel electrolytes containing sulfamate, chloride and combined sulfamate-chloride with concentrations between 0.14 M and 0.3 M were investigated. Physicochemical properties i.e. pH and conductivity were measured to ensure if they were in the desired value. The electrochemical behaviour of the electrolytes was measured by polarisation experiments in a standard three-electrode cell. The working electrode was a copper disc (surface area of 0.196 cm2 and the counter electrode was platinum mesh. The potential was measured againts a saturated calomel reference electrode (SCE. The experiments were carried out at various scan rate and Rotating Disc Electrode (RDE rotation speed to see the effect of scan rate and agitation. Based on the measured physicochemical properties, the electrolyte of 0.19 M nickel sulfamate was chosen for experimentation. Polarisation curve of agitated solution suggested that overall nickel electrodeposition reaction is controlled by a combination of kinetics and mass transfer.  Reduction potential of nickel was in the range of -0.7 to -1.0 V. The corresponding current densities for nickel deposition were in the range of -0.1 to -1.5 mA cm-2.

  19. Nanocomposite polymer electrolyte for rechargeable magnesium batteries

    Energy Technology Data Exchange (ETDEWEB)

    Shao, Yuyan; Rajput, Nav Nidhi; Hu, Jian Z.; Hu, Mary Y.; Liu, Tianbiao L.; Wei, Zhehao; Gu, Meng; Deng, Xuchu; Xu, Suochang; Han, Kee Sung; Wang, Jiulin; Nie, Zimin; Li, Guosheng; Zavadil, K.; Xiao, Jie; Wang, Chong M.; Henderson, Wesley A.; Zhang, Jiguang; Wang, Yong; Mueller, Karl T.; Persson, Kristin A.; Liu, Jun

    2014-12-28

    Nanocomposite polymer electrolytes present new opportunities for rechargeable magnesium batteries. However, few polymer electrolytes have demonstrated reversible Mg deposition/dissolution and those that have still contain volatile liquids such as tetrahydrofuran (THF). In this work, we report a nanocomposite polymer electrolyte based on poly(ethylene oxide) (PEO), Mg(BH4)2 and MgO nanoparticles for rechargeable Mg batteries. Cells with this electrolyte have a high coulombic efficiency of 98% for Mg plating/stripping and a high cycling stability. Through combined experiment-modeling investigations, a correlation between improved solvation of the salt and solvent chain length, chelation and oxygen denticity is established. Following the same trend, the nanocomposite polymer electrolyte is inferred to enhance the dissociation of the salt Mg(BH4)2 and thus improve the electrochemical performance. The insights and design metrics thus obtained may be used in nanocomposite electrolytes for other multivalent systems.

  20. Corrosion of stainless steel battery components by bis(fluorosulfonyl)imide based ionic liquid electrolytes

    Science.gov (United States)

    Evans, Tyler; Olson, Jarred; Bhat, Vinay; Lee, Se-Hee

    2014-12-01

    While the anodic behavior of aluminum foil current collectors in imide-based room temperature ionic liquids (RTILs) is relatively well understood, interactions between such RTILs and other passive battery components have not been studied extensively. This study presents the solvent and potential dependent oxidation of SS316 coin-cell components in the N-methyl-N-propyl-pyrrolidinium bis(fluorosulfonyl)imide (PYR13FSI) RTIL. While this phenomenon prohibits high-voltage cycling of Li(Ni1/3Mn1/3Co1/3)O2 cathodes in SS316 coin-type cells, Al-clad cell components or alternative cell configurations can be utilized to avoid SS316 oxidation-induced cell failure.

  1. Microfabrication of a Polymer Based Bi-Conductive Membrane for a Polymer Electrolyte Membrane Fuel Cell

    International Nuclear Information System (INIS)

    This paper reports a novel fabrication process of a high active area ratio bi-conductive membrane for PEMFCs. The fabricated device is a 50μm thick flexible polyimide based membrane that integrates for the first time lateral electrical conductive layers on both sides with a through ionic conductive path. With the use of thermo-conductive rubber as a bonding agent allowing a quick-flip process, five configurations of double-sided multilayer metal sputtering on polyimide were tested. An approach for filling through pores in the membrane with the ionic conductor (Nafion) with a temporary reservoir was also developed. The development of these new processes allowed to fabricate a membrane with 50μm wide holes filled with ionic conductor with double-sided electrical conductive layers

  2. Ionic liquid electrolytes as a platform for rechargeable metal-air batteries: a perspective.

    Science.gov (United States)

    Kar, Mega; Simons, Tristan J; Forsyth, Maria; MacFarlane, Douglas R

    2014-09-21

    Metal-air batteries are a well-established technology that can offer high energy densities, low cost and environmental responsibility. Despite these favourable characteristics and utilisation of oxygen as the cathode reactant, these devices have been limited to primary applications, due to a number of problems that occur when the cell is recharged, including electrolyte loss and poor efficiency. Overcoming these obstacles is essential to creating a rechargeable metal-air battery that can be utilised for efficiently capturing renewable energy. Despite the first metal-air battery being created over 100 years ago, the emergence of reactive metals such as lithium has reinvigorated interest in this field. However the reactivity of some of these metals has generated a number of different philosophies regarding the electrolyte of the metal-air battery. Whilst much is already known about the anode and cathode processes in aqueous and organic electrolytes, the shortcomings of these electrolytes (i.e. volatility, instability, flammability etc.) have led some of the metal-air battery community to study room temperature ionic liquids (RTILs) as non-volatile, highly stable electrolytes that have the potential to support rechargeable metal-air battery processes. In this perspective, we discuss how some of these initial studies have demonstrated the capabilities of RTILs as metal-air battery electrolytes. We will also show that much of the long-held mechanistic knowledge of the oxygen electrode processes might not be applicable in RTIL based electrolytes, allowing for creative new solutions to the traditional irreversibility of the oxygen reduction reaction. Our understanding of key factors such as the effect of catalyst chemistry and surface structure, proton activity and interfacial reactions is still in its infancy in these novel electrolytes. In this perspective we highlight the key areas that need the attention of electrochemists and battery engineers, in order to progress

  3. SiNWs-based electrochemical double layer micro-supercapacitors with wide voltage window (4 V) and long cycling stability using a protic ionic liquid electrolyte

    International Nuclear Information System (INIS)

    The present work reports the use and application of a novel protic ionic liquid (triethylammonium bis(trifluoromethylsulfonyl)imide; NEt3H TFSI) as an electrolyte for symmetric planar micro-supercapacitors based on silicon nanowire electrodes. The excellent performance of the device has been successfully demonstrated using cyclic voltammetry, galvanostatic charge-discharge cycles and electrochemical impedance spectroscopy. The electrochemical characterization of this system exhibits a wide operative voltage of 4 V as well as an outstanding long cycling stability after millions of galvanostatic cycles at a high current density of 2 mA cm−2. In addition, the electrochemical double layer micro-supercapacitor was able to deliver a high power density of 4 mW cm−2 in a very short time pulses (a few ms). Our results could be of interest to develop prospective on-chip micro-supercapacitors using protic ionic liquids as electrolytes with high performance in terms of power and energy densities. (paper)

  4. Stable trifluorostyrene containing compounds grafted to base polymers, and their use as polymer electrolyte membranes

    Science.gov (United States)

    Yang, Zhen-Yu; Roelofs, Mark Gerrit

    2010-11-09

    A fluorinated ion exchange polymer prepared by grafting at least one grafting monomer on to at least one base polymer, wherein the grafting monomer comprises structure 1a or 1b: wherein Z comprises S, SO.sub.2, or POR wherein R comprises a linear or branched perfluoroalkyl group of 1 to 14 carbon atoms optionally containing oxygen or chlorine, an alkyl group of 1 to 8 carbon atoms, an aryl group of 6 to 12 carbon atoms or a substituted aryl group of 6 to 12 carbon atoms; RF comprises a linear or branched perfluoroalkene group of 1 to 20 carbon atoms, optionally containing oxygen or chlorine; Q is chosen from F, --OM, NH.sub.2, --N(M)SO.sub.2R.sup.2.sub.F, and C(M)(SO.sub.2R.sup.2.sub.F).sub.2, wherein M comprises H, an alkali cation, or ammonium; R.sup.2.sub.F groups comprises alkyl of 1 to 14 carbon atoms which may optionally include ether oxygens or aryl of 6 to 12 carbon atoms where the alkyl or aryl groups may be perfluorinated or partially fluorinated; and n is 1 or 2 for 1a, and n is 1, 2, or 3 for 1b. These ion exchange polymers are useful in preparing catalyst coated membranes and membrane electrode assemblies used in fuel cells.

  5. Performance evaluation of titanium dioxide based dye-sensitized solar cells under the influence of anodization steps, nanotube length and ionic liquid-free redox electrolyte solvents

    Science.gov (United States)

    Cheong, Y. L.; Beh, K. P.; Yam, F. K.; Hassan, Z.

    2016-06-01

    In this work, highly ordered titanium dioxide (TiO2) nanotube (NT) arrays were synthesized on titanium foil using electrochemical anodization method. The morphological aspects of the nanotubes based on different anodization duration and number of anodization steps (maximum two) have been investigated. The nanotube arrays subsequently used as photoanode in a dye-sensitized solar cell (DSSC) assembly. The studies on the effects of different solvents for triiodide/iodide redox electrolyte and NT length towards the performance of DSSC were conducted. It is known that electrolyte solvent can significantly affect the photovoltaic conversion efficiency. It is noteworthy that longer NT length tends to yield higher efficiency due to better dye adsorption. However, when the NTs exceeded certain length the efficiency decreases instead. Meanwhile, a comparison of DSSC performance based on number of anodization steps on titanium was performed. Highly ordered NT arrays could be obtained using two-steps anodization, which proved to have positive effects on the DSSC performance. The highest photovoltaic conversion efficiency in this work is 2.04%, achieved by two-step anodization. The corresponding average nanotubes length was ˜18 μm, with acetonitrile (ACN) as the redox electrolyte solvent.

  6. Temperature dependence of the electrode potential of a cobalt-based redox couple in ionic liquid electrolytes for thermal energy harvesting.

    Science.gov (United States)

    He, Jiangjing; Al-Masri, Danah; MacFarlane, Douglas R; Pringle, Jennifer M

    2016-08-15

    Increasing the application of technologies for harvesting waste heat could make a significant contribution to sustainable energy production. Thermoelectrochemical cells are one such emerging technology, where the thermal response of a redox couple in an electrolyte is used to generate a potential difference across a cell when a temperature gradient exists. The unique physical properties of ionic liquids make them ideal for application as electrolytes in these devices. One of the keys to utilizing these media in efficient thermoelectrochemical cells is achieving high Seebeck coefficients, Se: the thermodynamic quantity that determines the magnitude of the voltage achieved per unit temperature difference. Here, we report the Se and cell performance of a cobalt-based redox couple in a range of different ionic liquids, to investigate the influence of the nature of the IL on the thermodynamics and cell performance of the redox system. The results reported include the highest Se to-date for an IL-based electrolyte. The effect of diluting the different ILs with propylene carbonate is also reported, which results in a significant increase in the output powers and current densities of the device. PMID:27200437

  7. ZrO2基固体电解质的研究进展%Development of zirconia oxide based solid electrolyte

    Institute of Scientific and Technical Information of China (English)

    乐士儒; 张靖; 朱晓东; 张乃庆; 孙克宁

    2012-01-01

    固体氧化物燃料电池(SOFC)是目前国际上燃料电池领域的研究热点,电解质是SOFC中最关键的元件,提高ZrO2基固体电解质的电导率是SOFC研究的核心的问题之一.从热力学、动力学、理论模型等方面综述了近年来ZrO2基电解质的研究进展,并对实现ZrO2基固体电解质电导率的提高提出了解决问题的路线.%Solid oxide fuel cell (SOFC) is the research focus in the fuel cell fields. Electrolyte is the most important component, and how to improve the conductivity of ZrO2 base electrolyte is one focus problem. In this paper, the development of zirconia based electrolyte from the thermodynamics, dynamics, and theoretical model, etc was reviewed, and the solution of how to improve the conductivity was offered.

  8. Vibrational studies of flexible solid polymer electrolyte based on PCL-EC incorporated with proton conducting NH4SCN

    Science.gov (United States)

    Woo, H. J.; Arof, A. K.

    2016-05-01

    A flexible solid polymer electrolyte (SPE) system based on poly(ε-caprolactone) (PCL), a FDA approved non-toxic and biodegradable material in the effort to lower environmental impact was prepared. Ammonium thiocyanate (NH4SCN) and ethylene carbonate (EC) were incorporated as the source of charge carriers and plasticizing agent, respectively. When 50 wt.% of ethylene carbonate (EC) was added to PCL-NH4SCN system, the conductivity increased by two orders from of 3.94 × 10- 7 Scm- 1 to 3.82 × 10- 5 Scm- 1. Molecular vibrational analysis via infrared spectroscopy had been carried out to study the interaction between EC, PCL and NH4SCN. The relative percentage of free ions, ion pairs and ion aggregates was calculated quantitatively by deconvoluting the SCN- stretching mode (2030-2090 cm- 1). This study provides fundamental insight on how EC influences the free ion dissociation rate and ion mobility. The findings are also in good agreement to conductivity, differential scanning calorimetry and X-ray diffraction results. High dielectric constant value (89.8) of EC had made it an effective ion dissociation agent to dissociate both ion pairs and ion aggregates, thus contributing to higher number density of free ions. The incorporation of EC had made the polymer chains more flexible in expanding amorphous domain. This will facilitate the coupling synergy between ionic motion and polymer segmental motion. Possible new pathway through EC-NH4+ complex sites for ions to migrate with shorter distance has been anticipated. This implies an easier ion migration route from one complex site to another.

  9. Progress of the electrochemical reduction of CO2 in aqueous electrolyte%水溶液中电化学还原CO2的研究进展

    Institute of Scientific and Technical Information of China (English)

    张现萍; 黄海燕; 靳红利; 俞英; 陈英敦

    2015-01-01

    CO2作为一种潜在的碳资源,寻找一种有效的方法转移利用 CO2一直是社会关注的焦点.水溶液中电化学方法转化固定 CO2可在室温和常压下进行,通过选择不同电极和电极电势来改变产物、调控反应速率和选择性,因而具有潜在的优势.本文综述了水溶液中电化学还原 CO2的发展现状,介绍了水溶液中电还原 CO2的基本原理和电极上发生的主要反应;总结了水溶液中金属电极、气体扩散电极(GDEs)和复合电极等不同电极材料对 CO2还原产物的种类、选择性以及电流效率的影响;讨论了温度、CO2分压等还原反应条件对反应速率和电流效率的影响.展望了水溶液中电还原CO2技术的发展前景,认为利用水基溶液中丰富的[H],增强CO2还原产物的燃料化程度,将在环境保护、资源利用和经济效益方面具有极大价值,符合绿色化学发展理念.%AsCO2 is a vital reagent for the production of useful chemicals,it is high time to find an efficient way to make use of it. The electrochemical reduction of CO2,which can be conducted under the ambient conditions and converse CO2 into various products,provides a promising future both for the utilization of CO2 and for the human beings. The products,the reaction rate and the selectivity of the reaction can be adjusted by conducting the reaction on different electrodes and at different over potentials. This paper highlights the progress of the electrochemical reduction of CO2 in aqueous electrolyte and summarizes the mechanism of electrochemical reduction of CO2 proposed by various workers and introduces the main reactions occurred during the reduction process. Studies carried out on different kinds of electrodes,such as metal electrodes,gas diffusion electrodes (GDEs) and composite electrodes and so on,have also been reviewed. The products,the selectivity of the reaction and the currency during the process of reduction,also vary with the materials

  10. Molten salt electrolyte separator

    Science.gov (United States)

    Kaun, Thomas D.

    1996-01-01

    A molten salt electrolyte/separator for battery and related electrochemical systems including a molten electrolyte composition and an electrically insulating solid salt dispersed therein, to provide improved performance at higher current densities and alternate designs through ease of fabrication.

  11. Mechanisms of proton conductance in polymer electrolyte membranes

    DEFF Research Database (Denmark)

    Eikerling, M.; Kornyshev, A. A.; Kuznetsov, A. M.;

    2001-01-01

    We provide a phenomenological description of proton conductance in polymer electrolyte membranes, based on contemporary views of proton transfer processes in condensed media and a model for heterogeneous polymer electrolyte membrane structure. The description combines the proton transfer events i...

  12. Synthesis and analysis of processes with electrolyte mixtures

    DEFF Research Database (Denmark)

    Thomsen, Kaj; Gani, Rafiqul; Rasmussen, Peter

    1995-01-01

    A computer aided system for synthesis, design and simulation of crystallization and fractional crystallization processes with electrolyte mixtures is presented. The synthesis methodology is based on the use of computed solubility diagrams for the corresponding electrolyte systems....

  13. Versatile Flow-Injection Amperometric Ion Detector Based on an Interface between Two Immiscible Electrolyte Solutions: Numerical and Experimental Characterization

    DEFF Research Database (Denmark)

    Deryabina, Maria; Hansen, Steen H.; Jensen, Henrik

    2011-01-01

    The present paper describes a flexible thin layer electrochemical flow cell for ultrasensitive amperometric detection at a supported interface between immiscible electrolyte solutions. Nanomolar detection limits were demonstrated using the cell design, and 3D finite element simulations allowed a ...... electrochemical flow cell detector with a large surface to volume ratio....

  14. Direct measurement of the chemical reactivity of silicon electrodes with LiPF6-based battery electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Veith, Gabriel M [ORNL; Baggetto, Loic [ORNL; Sacci, Robert L [ORNL; Unocic, Raymond R [ORNL; Tenhaeff, Wyatt E [ORNL; Browning, Jim [ORNL

    2014-01-01

    We report the first direct measurement of the chemistry and extent of reactivity between a lithium ion battery electrode surface (Si) and a liquid electrolyte (1.2M LiPF6-3:7 wt% ethylene carbonate:dimethyl carbonate). This layer is estimated to be 3.6 nm thick and partially originates from the consumption of the silicon surface.

  15. Electrical Conductivity Study of Polymer Electrolyte Magnetic Nanocomposite Based Poly(Vinyl) Alcohol (PVA) Doping Lithium and Nickel Salt

    Science.gov (United States)

    Aji, Mahardika Prasetya; Rahmawati, Silvia, Bijaksana, Satria; Khairurrijal, Abdullah, Mikrajuddin

    2010-10-01

    Composite polymer electrolyte magnetic systems composed of poly(vinyl) alcohol (PVA) as the host polymer, lithium and nickel salt as dopant were studied. The effect upon addition of lithium ions in polimer PVA had been enhanced conductivity with the increase of lithium concentration. The conductivity values were 1.19x10-6, 1.25x10-5, 4.89x-5, 1.88x10-4, and 1.33x10-3 Sṡcm-1 for pure PVA and 1%, 3%, 5% and 7% LiOH complexed PVA, respectively. Meanwhile, the addition nickel salt into polymer electrolyte PVA-LiOH does not significantly change of conductivity value, on order 10-3 Sṡcm-1. The ionic transport is dominantly regarded by Li+ ions present in polymer electrolyte magnetic because the atomic mass Li+ is smaller than Ni2+. The absence of external magnetic field in polimer electrolyte magnetic causes the existence Ni2+ ions not significantly affected of conductivity.

  16. A novel temperature-gradient Na±β-alumina solid electrolyte based SOx gas sensor without gaseous reference electrode

    DEFF Research Database (Denmark)

    Rao, N.; Bleek, C.M. Van den; Schoonman, J.;

    1992-01-01

    An electrochemical SOx ps sensor with a tubular Na+-beta"-alumina solid electrolyte has been fabricated and tested under non-isothermal conditions. The temperature difference between the reference and working electrode of the sensor cell is about 100-degrees-C, which causes a serious deviation...

  17. Standard practice for electrolytic extraction of phases from Ni and Ni-Fe base superalloys using a hydrochloric-methanol electrolyte

    CERN Document Server

    American Society for Testing and Materials. Philadelphia

    1995-01-01

    1.1 This practice covers a procedure for the isolation of carbides, borides, TCP (topologically close-packed), and GCP (geometrically close-packed) phases (Note 1) in nickel and nickel-iron base gamma prime strengthened alloys. Contamination of the extracted residue by coarse matrix (gamma) or gamma prime particles, or both, reflects the condition of the alloy rather than the techniques mentioned in this procedure. 1.2 This standard does not purport to address all of the safety concerns, if any, associated with its use. It is the responsibility of the user of this standard to establish appropriate safety and health practices and determine the applicability of regulatory limitations prior to use.

  18. Evaluation of Diesel Engine Noise Reduction Measures Based on Hierarchy Diagnosis

    Institute of Scientific and Technical Information of China (English)

    2007-01-01

    Effect of different noise reduction measures for diesel engines was evaluated based on hierarchy diagnosis. The hierarchy diagnosis chart and hierarchy judgment matrix were given.Through evaluation of noise reduction measures, the main strategies of noise reduction were found.The result shows that the noise reduction level of different frequency belts varies from measure to measure. The reduction capacity of different measures could not add simply, which relates to the problem of parameter matching.

  19. Final Technical Report: SISGR: The Influence of Electrolyte Structure and Electrode Morphology on the Performance of Ionic-Liquid Based Supercapacitors: A Combined Experimental and Simulation Study

    Energy Technology Data Exchange (ETDEWEB)

    Bedrov, Dmitry [University of Utah

    2013-08-15

    Obtaining fundamental understanding and developing predictive modeling capabilities of electrochemical interfaces can significantly shorten the development cycles of electrical double layer capacitors (EDLCs). A notable improvement in EDLC performance has been achieved due to recent advances in understanding charge storage mechanisms, development of advanced nanostructured electrodes and electrochemically stable electrolytes. The development of new generation of EDLCs is intimately linked to that of nanostructured carbon materials which have large surface area, good adsorption/desorption properties, good electrical conductivity and are relatively inexpensive. To address these scientific challenges the efforts of an interdisciplinary team of modelers and experimentalists were combined to enhance our understanding of molecular level mechanisms controlling the performance of EDLCs comprised of room temperature ionic liquid (RTIL) electrolytes and nanostructured carbon-based electrodes and to utilize these knowledge in the design of a new generation of materials and devices for this energy storage application. Specifically our team efforts included: atomistic molecular dynamics simulations, materials science and electrode/device assembly, and synthesis and characterization of RTIL electrolytes.

  20. Study the effect of ion-complex on the properties of composite gel polymer electrolyte based on Electrospun PVdF nanofibrous membrane

    International Nuclear Information System (INIS)

    In this paper, nanofibrous membranes based on poly(vinylidene fluoride) (PVdF) doped with ion-complex (SiO2-PAALi) were prepared by electrospinning technique and the corresponding composite gel-polymer electrolytes (CGPEs) were obtained after being activated in liquid electrolyte. The microstructure, physical and electrochemical performances of the nanofibrous membranes and the corresponding CGPEs were studied by various measurements such as Fourier Transform Infrared Spectroscopy(FTIR), Scanning Electron Microscope (SEM), Differential Scanning Calorimetry (DSC), Thermal Gravimetric Analysis (TGA), Stress-strain test, Linear Sweep Voltammetry (LSV), AC impedance measurement and Charge/discharge cycle test. As to the ion-complex doped nanofibrous membranes, PVdF can provide mechanical support with network structure composed of fully interconnection; while the ion-complexes are absorbed onto the surface of the PVdF nanofibers evenly instead of being aggregated. With the help of doped ion-complex, the prepared nanofibrous membranes present good liquid electrolyte absorbability, excellent mechanical performance, and high decomposition temperature. For the corresponding CGPEs, they possess high ionic conductivity, wide electrochemical window, and good charge/discharge cycle performance

  1. Two-dimensional ion chromatography for the separation of ionic organophosphates generated in thermally decomposed lithium hexafluorophosphate-based lithium ion battery electrolytes.

    Science.gov (United States)

    Kraft, Vadim; Grützke, Martin; Weber, Waldemar; Menzel, Jennifer; Wiemers-Meyer, Simon; Winter, Martin; Nowak, Sascha

    2015-08-28

    A two-dimensional ion chromatography (IC/IC) technique with heart-cutting mode for the separation of ionic organophosphates was developed. These analytes are generated during thermal degradation of three different commercially available Selectilyte™ lithium ion battery electrolytes. The composition of the investigated electrolytes is based on 1M lithium hexafluorophosphate (LiPF6) dissolved in ethylene carbonate/dimethyl carbonate (50:50wt%, LP30), ethylene carbonate/diethyl carbonate (50:50wt%, LP40) and ethylene carbonate/ethyl methyl carbonate (50:50wt%, LP50). The organophosphates were pre-separated from PF6(-) anion on the low capacity A Supp 4 column, which was eluted with a gradient step containing acetonitrile. The fraction containing analytes was retarded on a pre-concentration column and after that transferred to the high capacity columns, where the separation was performed isocratically. Different stationary phases and eluents were applied on the 2nd dimension for the investigation of retention times, whereas the highly promising results were obtained with a high capacitive A Supp 10 column. The organophosphates generated in LP30 and LP40 electrolytes could be separated by application of an aqueous NaOH eluent providing fast analysis time within 35min. For the separation of the organophosphates of LP50 electrolyte due to its complexity a NaOH eluent containing a mixture of methanol/H2O was necessary. In addition, the developed two dimensional IC method was hyphenated to an inductively coupled plasma mass spectrometer (ICP-MS) using aqueous NaOH without organic modifiers. This proof of principle measurement was carried out for future quantitative investigation regarding the concentration of the ionic organophosphates. Furthermore, the chemical stability of several ionic organophosphates in water and acetonitrile at room temperature over a period of 10h was investigated. In both solvents no decomposition of the investigated analytes was observed and

  2. Preparation of highly active and stable polyaniline-cobalt-carbon nanotube electrocatalyst for oxygen reduction reaction in polymer electrolyte membrane fuel cell

    International Nuclear Information System (INIS)

    This paper established an in-situ synthesis strategy that the mixing solution of aniline, CNTs and CoCl2 was directly reduced to prepare polyaniline-cobalt-carbon nanotube (PANI-Co-CNT) electrocatalyst. Furthermore, this strategy was effectively modified by pretreating CoCl2 precursor with citric acid (CA), forming 2-4 nm cobalt nanoparticles uniformly distributed on PANI-CNT support with porous structure. The control experiments revealed various PANI states in the growth stage, further proposing the self-assembly mechanisms in these two routes with and without CA pretreatment. These two PANI-Co-CNT electrocatalysts were also checked by oxygen reduction reaction (ORR) in acid environment, to corroborate their basically 4-electron processes. Inspiringly, the large activity and stability for the pretreated route could be comparable with those of the advanced electrocatalysts. All these progresses lay a bottom-up approach for future electrocatalysts

  3. A pilot study on mindfulness based stress reduction for smokers

    Directory of Open Access Journals (Sweden)

    Baker Timothy B

    2007-01-01

    Full Text Available Abstract Background Mindfulness means paying attention in the present moment, non-judgmentally, without commentary or decision-making. We report results of a pilot study designed to test the feasibility of using Mindfulness Based Stress Reduction (MBSR (with minor modifications as a smoking intervention. Methods MBSR instructors provided instructions in mindfulness in eight weekly group sessions. Subjects attempted smoking cessation during week seven without pharmacotherapy. Smoking abstinence was tested six weeks after the smoking quit day with carbon monoxide breath test and 7-day smoking calendars. Questionnaires were administered to evaluate changes in stress and affective distress. Results 18 subjects enrolled in the intervention with an average smoking history of 19.9 cigarettes per day for 26.4 years. At the 6-week post-quit visit, 10 of 18 subjects (56% achieved biologically confirmed 7-day point-prevalent smoking abstinence. Compliance with meditation was positively associated with smoking abstinence and decreases in stress and affective distress. Discussions and conclusion The results of this study suggest that mindfulness training may show promise for smoking cessation and warrants additional study in a larger comparative trial.

  4. Mindfulness-based stress reduction for people with chronic diseases.

    Science.gov (United States)

    Merkes, Monika

    2010-01-01

    Mindfulness-based stress reduction (MBSR) is a structured group program that uses mindfulness meditation to improve well-being and alleviate suffering. This article reviews the impact of MBSR for people with chronic diseases. The review includes original research that was published in English and peer-reviewed and reported outcomes for adults with chronic diseases who had participated in an MBSR program. Fifteen studies were identified. Outcomes related to mental and physical health, well-being, and quality of life. The studies included different research designs, and used self-report and physiological outcome measures. Participants' clinical diagnoses included fibromyalgia, chronic pain, rheumatoid arthritis, type 2 diabetes, chronic fatigue syndrome, multiple chemical sensitivity, and cardiovascular diagnoses. All 15 studies found that participation in an MBSR program resulted in improvements. No negative change was reported between baseline and follow up. Outcomes in regard to specific variables were difficult to compare and equivocal. Overall, positive change predominated. Chronic diseases are associated with a range of unwelcome psychological and physical consequences. Participation in an MBSR program is likely to result in coping better with symptoms, improved overall well-being and quality of life, and enhanced health outcomes. As an adjunct to standard care, MBSR has potential for much wider application in Australian primary care settings.

  5. First principles based mean field model for oxygen reduction reaction.

    Science.gov (United States)

    Jinnouchi, Ryosuke; Kodama, Kensaku; Hatanaka, Tatsuya; Morimoto, Yu

    2011-12-21

    A first principles-based mean field model was developed for the oxygen reduction reaction (ORR) taking account of the coverage- and material-dependent reversible potentials of the elementary steps. This model was applied to the simulation of single crystal surfaces of Pt, Pt alloy and Pt core-shell catalysts under Ar and O(2) atmospheres. The results are consistent with those shown by past experimental and theoretical studies on surface coverages under Ar atmosphere, the shape of the current-voltage curve for the ORR on Pt(111) and the material-dependence of the ORR activity. This model suggests that the oxygen associative pathway including HO(2)(ads) formation is the main pathway on Pt(111), and that the rate determining step (RDS) is the removal step of O(ads) on Pt(111). This RDS is accelerated on several highly active Pt alloys and core-shell surfaces, and this acceleration decreases the reaction intermediate O(ads). The increase in the partial pressure of O(2)(g) increases the surface coverage with O(ads) and OH(ads), and this coverage increase reduces the apparent reaction order with respect to the partial pressure to less than unity. This model shows details on how the reaction pathway, RDS, surface coverages, Tafel slope, reaction order and material-dependent activity are interrelated. PMID:22064886

  6. Nanoporous polymer electrolyte

    Science.gov (United States)

    Elliott, Brian; Nguyen, Vinh

    2012-04-24

    A nanoporous polymer electrolyte and methods for making the polymer electrolyte are disclosed. The polymer electrolyte comprises a crosslinked self-assembly of a polymerizable salt surfactant, wherein the crosslinked self-assembly includes nanopores and wherein the crosslinked self-assembly has a conductivity of at least 1.0.times.10.sup.-6 S/cm at 25.degree. C. The method of making a polymer electrolyte comprises providing a polymerizable salt surfactant. The method further comprises crosslinking the polymerizable salt surfactant to form a nanoporous polymer electrolyte.

  7. Solid state electrolyte systems

    Energy Technology Data Exchange (ETDEWEB)

    Pederson, L.R.; Armstrong, B.L.; Armstrong, T.R. [Pacific Northwest Lab., Richland, WA (United States)] [and others

    1997-12-01

    Lanthanum gallates are a new family of solid electrolytes that exhibit high ionic conductivity and are stable to high temperatures. Compositions have been developed that are as much as a factor of two more conductive than yttria-stabilized zirconia at a given temperature, through partial replacement of lanthanum by calcium, strontium, and/or barium and through partial replacement of gallium by magnesium. Oxide powders were prepared using combustion synthesis techniques developed in this laboratory; these were sintered to >95% of theoretical density and consisted of a single crystalline phase. Electrical conductivities, electron and ion transference numbers, thermal expansion, and phase behavior were evaluated as a function of temperature and oxygen partial pressure. A key advantage of the use of lanthanum gallate electrolytes in solid oxide fuel cells is that the temperature of operation may be lowered to perhaps 800 C, yet provide approximately the same power density as zirconia-based cells operating at 1000 C. Ceramic electrolytes that conduct both oxygen ions and electrons are potentially useful to passively separate pure oxygen from an air source at low cost. In such materials, an oxygen ion flux in one direction is charge-compensated by an opposing electron flux. The authors have examined a wide range of mixed ion and electron conducting perovskite ceramics in the system La{sub 1{minus}x}M{sub x}Co{sub 1{minus}y{minus}z}Fe{sub y}N{sub z}O{sub 3{minus}{delta}}, where M = Sr, Ca, and Ba, and N = Pr, Mn, Ni, Cu, Ti, and Al, as well as mixed conducting brownmillerite ceramics, and have characterized oxygen permeation behavior, defect chemistry, structural and phase stability, and performance as cathodes.

  8. Electrolytic indium refining from cadmium in glycerine electrolyte

    International Nuclear Information System (INIS)

    The results of investigations directed on development of electrochemical indium cleaning from cadmium in glycerine base electrolyte are presented. Optimal operational conditions, specific consumption of reactants and electric power are determined. Relationship between variation of concentration of cadmium impurity in refined metal and duration of electrolysis is revealed. The method for determination of cleaning time is proposed. Developed process was put into commercial operation

  9. Study of ageing mechanisms of organic electrolyte super-capacitors based on activated carbons; Recherche des causes du vieillissement de supercondensateurs a electrolyte organique a base de carbones actives

    Energy Technology Data Exchange (ETDEWEB)

    Azais, Ph.

    2003-11-15

    The energy which is stored in electrochemical capacitors is proportional to the square of voltage. Consequently, the most attractive super-capacitors are those which operate in organic electrolyte medium, with an electrolyte potential window which theoretically can easily reach more than 3 V. However, even using lower values of voltage, there is a remarkable fading of the electrochemical characteristics with operating time, that is mainly characterized by capacitance loss and resistance increase. On a commercial point of view, these capacitors must be improved in order to reach the expected criterion of long operating life. In the presented work, we will determine some reasons of super-capacitors ageing in organic electrolyte (1 M solution of Et{sub 4}N{sup +} BF{sub 4}{sup -} in acetonitrile) and we will propose a treatment of activated carbon which noticeably improves the performance. A prolonged charging of electrochemical capacitors at 2.5 V, so called floating, results in gases formation and to a noticeable mass uptake of the electrodes. XPS and NMR analysis performed on carefully washed electrodes demonstrated the existence of decomposition products from the electrolyte, which are trapped in the pores of the activated carbon. These products block the pores, limiting the ions access to the active surface that causes the decay of electrochemical performances. Electrolyte decomposition is especially very high when the electrodes are constituted of carbons with a rich surface functionality, i.e. surface oxygenated groups and free radicals. Therefore, activated carbons have been submitted to thermal treatment, both in nitrogen and hydrogen atmosphere, allowing the oxygenated surface functionality to be noticeably depressed. Super-capacitors built with the treated materials have been submitted to floating during more than 2000 hours. Extremely good electrochemical performance are preserved with the electrodes obtained from activated carbons treated under hydrogen

  10. Electrolytes in solid-state dye-sensitized nanocrystalline solar cells

    Institute of Scientific and Technical Information of China (English)

    AN Hongli; XUE Bofei; LI Dongmei; MENG Qingbo; GUO Lin

    2006-01-01

    In this paper, the structure and operating principle of the dye-sensitized nanocrystalline solar cells (DSSC) are discussed. The electrolytes can be divided into three types: liquid electrolyte, quasi-solid electrolyte and solid electrolyte. Based on the rele vant study of our group, we summarized mainly the research progress of the quasi-solid electrolyte and solid electrolyte in solid-state DSSC.

  11. Semiconductor electrolyte photovoltaic energy converter

    Science.gov (United States)

    Anderson, W. W.; Anderson, L. B.

    1975-01-01

    Feasibility and practicality of a solar cell consisting of a semiconductor surface in contact with an electrolyte are evaluated. Basic components and processes are detailed for photovoltaic energy conversion at the surface of an n-type semiconductor in contact with an electrolyte which is oxidizing to conduction band electrons. Characteristics of single crystal CdS, GaAs, CdSe, CdTe and thin film CdS in contact with aqueous and methanol based electrolytes are studied and open circuit voltages are measured from Mott-Schottky plots and open circuit photo voltages. Quantum efficiencies for short circuit photo currents of a CdS crystal and a 20 micrometer film are shown together with electrical and photovoltaic properties. Highest photon irradiances are observed with the GaAs cell.

  12. Proton Conducting Polymer Electrolytes and Its Applications

    Institute of Scientific and Technical Information of China (English)

    S. Selvasekarapandian; G. Hirankumar; R. Baskaran; M.S. Bhuvaneswari

    2005-01-01

    @@ 1Introduction Proton conducting solid polymer electrolytes have been extensively studied due to their potential applications in electrochemical devices such as batteries, super capacitors, electrochromic windows, sensors etc[1,2]Many researchers have studied the behaviour of inorganic based polymer electrolytes as proton conductors and their applications in solid state devices at room temperature[3]. But, inorganic acid doped electrolytes have some serious disadvantages like corrosion towards the electrode and hazardous. Hence, there is need for searching new electrolyte which is stable towards the electrode. It has been reported that the ammonium salts which behaves like alkali metal salt are good dopant to the polymer matrix[4, 5] for the development of proton conducting polymer electrolyte. The proton conductors based on poly (ethylene oxide)[6], poly (ethylene succinate)[7], poly (ethylene glycol)[8], as host matrix doped with ammonium salt have already been reported.

  13. Investigation of gas concentration cell based on LiSiPO electrolyte and Li2CO3, Au electrode

    Institute of Scientific and Technical Information of China (English)

    ZHU YongMing; CHU WingFong; WEPPNER Werner

    2009-01-01

    Solid lithium ion conducting electrochemical cells using LiSiPO as solid electrolyte and Li2CO3 mixed with Au as electrodes were prepared and employed as chemical sensors for the detection of CO2 gas.The EMF of the cell depends on the concentration of CO2 in air according to the partial pressure de-pendence of Nernst's law in the investigated range from 100 to 2000 ppm over the temperature range from 473 K to 673 K.

  14. Direct measurement of the chemical reactivity of silicon electrodes with LiPF6-based battery electrolytes.

    Science.gov (United States)

    Veith, Gabriel M; Baggetto, Loïc; Sacci, Robert L; Unocic, Raymond R; Tenhaeff, Wyatt E; Browning, James F

    2014-03-21

    We report the first direct measurement of the extent of the spontaneous non-electrochemically driven reaction between a lithium ion battery electrode surface (Si) and a liquid electrolyte (1.2 M LiPF6-3 : 7 wt% ethylene carbonate : dimethyl carbonate). This layer is estimated to be 35 Å thick with a SLD of ∼ 4 × 10(-6) Å(-2) and likely originates from the consumption of the silicon surface. PMID:24513965

  15. A Review on Current Status of Stability and Knowledge on Liquid Electrolyte-Based Dye-Sensitized Solar Cells

    Directory of Open Access Journals (Sweden)

    Frédéric Sauvage

    2014-01-01

    Full Text Available The purpose of this review is to gather the current background in materials development and provide the reader with an accurate image of today’s knowledge regarding the stability of dye-sensitized solar cells. This contribution highlights the literature from the 1970s to the present day on nanostructured TiO2, dye, Pt counter electrode, and liquid electrolyte for which this review is focused on.

  16. Performance of polymer electrolyte based on chitosan blended with poly(ethylene oxide) for plasmonic dye-sensitized solar cell

    Science.gov (United States)

    Buraidah, M. H.; Teo, L. P.; Au Yong, C. M.; Shah, Shahan; Arof, A. K.

    2016-07-01

    Chitosan and poly(ethylene oxide) powders have been mixed in different weight ratios. To each mixture, a fixed amount of ammonium iodide has been added. All mixtures have been dissolved in 1% acetic acid solution to form polymer blend electrolyte films by the solution cast technique. X-ray diffraction indicates that the polymer blend electrolytes are amorphous. Fourier transform infrared spectroscopy shows shifting of the amine, carboxamide and Csbnd Osbnd C bands to lower wavenumbers indicating the occurrence of complexation. Electrochemical impedance spectroscopy has been used to study the electrical properties of the samples. The ionic conductivity for 55 wt.% chitosan-45 wt.% NH4I electrolyte system is 3.73 × 10-7 S cm-1 at room temperature and is increased to 3.66 × 10-6 S cm-1 for the blended film (16.5 wt.% chitosan-38.5 wt.% PEO)-45 wt.% NH4I film. Dye-sensitized solar cells (DSSCs) have been fabricated by sandwiching the polymer electrolyte between the TiO2/dye photoelectrode and Pt counter electrode. DSSCs fabricated exhibits short-circuit current density (Jsc) of 2.71 mA cm-2, open circuit voltage (Voc) of 0.58 V and efficiency of 0.78% with configuration ITO/TiO2/N3 dye/(16.5 wt.% chitosan-38.5 wt.% PEO)-45 wt.% NH4I(+I2)/Pt/ITO and Jsc of 2.84 mA cm-2, Voc of 0.58 V and efficiency of 1.13% with configuration ITO/TiO2 + Ag nanoparticles/N3 dye/(16.5 wt.% chitosan-38.5 wt.% PEO)-45 wt.% NH4I(+I2)/Pt/ITO.

  17. Risk Reduction and Training using Simulation Based Tools - 12180

    International Nuclear Information System (INIS)

    Process Modeling and Simulation (M and S) has been used for many years in manufacturing and similar domains, as part of an industrial engineer's tool box. Traditionally, however, this technique has been employed in small, isolated projects where models were created from scratch, often making it time and cost prohibitive. Newport News Shipbuilding (NNS) has recognized the value of this predictive technique and what it offers in terms of risk reduction, cost avoidance and on-schedule performance of highly complex work. To facilitate implementation, NNS has been maturing a process and the software to rapidly deploy and reuse M and S based decision support tools in a variety of environments. Some examples of successful applications by NNS of this technique in the nuclear domain are a reactor refueling simulation based tool, a fuel handling facility simulation based tool and a tool for dynamic radiation exposure tracking. The next generation of M and S applications include expanding simulation based tools into immersive and interactive training. The applications discussed here take a tool box approach to creating simulation based decision support tools for maximum utility and return on investment. This approach involves creating a collection of simulation tools that can be used individually or integrated together for a larger application. The refueling simulation integrates with the fuel handling facility simulation to understand every aspect and dependency of the fuel handling evolutions. This approach translates nicely to other complex domains where real system experimentation is not feasible, such as nuclear fuel lifecycle and waste management. Similar concepts can also be applied to different types of simulation techniques. For example, a process simulation of liquid waste operations may be useful to streamline and plan operations, while a chemical model of the liquid waste composition is an important tool for making decisions with respect to waste disposition

  18. 7Li nuclear magnetic resonance studies of dynamics in a ternary gel polymer electrolyte based on polymeric ionic liquids

    International Nuclear Information System (INIS)

    The influence of the polymeric ionic liquid (PIL) Poly(diallyldimethylammonium bis(trifluoromethylsulfonyl) imide) (PDADMATFSI) on the lithium dynamics was investigated in a ternary gel polymer electrolyte consisting of PDADMATFSI as stabilizing polymer, ionic liquid (1-butyl-1-methylpyrrolidinium bis(trifluoromethylsulfonyl) imide, P14TFSI) and lithium salt (lithium bis(trifluoromethylsulfonyl) imide, LiTFSI). The diffusion coefficient of the lithium ions is investigated by pulsed-field-gradient NMR, the conductivity of the electrolyte is determined by impedance spectroscopy. The local lithium dynamics is characterized by 7Li spin lattice relaxation rates (R1). The relaxation rates are well described by Blombergen-Purcell-Pound (BPP) theory at all polymer concentrations (up to 45 mol%), implying that the Li dynamics is governed by one single motional mode. Interestingly, activation energies for this motion decrease from 20 kJ/mol to 15 kJ/mol with increasing polymer content and are independent on the salt content. We thus conclude that the polymer is interacting with the anion coordination shell, which is accompanied by a very beneficial effect on the local lithium dynamics, as the polymer PDADMATFSI reduces the Li-TFSI interactions. This result is promising for further investigations for potential use of PDADMATFSI-containing gels as electrolytes in energy storage devices

  19. Metal-free catalysts for oxygen reduction in alkaline electrolytes: Influence of the presence of Co, Fe, Mn and Ni inclusions

    International Nuclear Information System (INIS)

    Graphical abstract: - Highlights: • The presence of Fe in nitrogen modified carbon catalysts promotes their ORR activity. • In the presence of Fe, O2 is apparently reduced directly to OH− through the 4e transfer pathway. • The presence of Ni poisons the ORR activity of NC catalysts. - Abstract: Metal-free nitrogen modified carbon catalysts (NC) are very closely related to MNC catalysts which contain a transition metal(s) (M), usually Fe or Co as an essential constituent. We investigated the influence of metal inclusions on the activity of nitrogen-doped carbon black in the electrocatalysis of the oxygen reduction reaction (ORR). A reference metal-free NC catalyst was prepared by pyrolysis of a polypyrrole/Vulcan XC72 composite at 800 °C for 2 h under helium. Controlled amounts of Co, Fe, Mn and Ni in low concentrations were then introduced into NC by impregnating it with the corresponding meso-tetra(4-pyridyl) porphyrin metal complex followed by further pyrolysis at 650 °C for 2 h under helium. The resulting catalysts were investigated for ORR using rotating disk electrode and rotating-ring disk electrode voltammetry in 0.1 M KOH. Additionally, the rate of decomposition of hydrogen peroxide by the different catalysts was determined in order to probe the influence of the metal inclusions on the mechanism and selectivity of the ORR. The results show that Fe, Co and Mn inclusions cause a substantial decrease of the overpotential of the reaction and enhance the catalytic current, whereas the presence of Ni has a poisoning effect on ORR. In the presence of Fe, the catalysts apparently reduce oxygen selectively to OH− in a direct four electron transfer process as opposed to the two-step, two electron pathway involving hydrogen peroxide as an intermediate for the case of the NC catalyst

  20. Boron Clusters as Highly Stable Magnesium-Battery Electrolytes**

    OpenAIRE

    Carter, Tyler J; Mohtadi, Rana; Arthur, Timothy S; Mizuno, Fuminori; Zhang, Ruigang; Shirai, Soichi; Kampf, Jeff W.

    2014-01-01

    Boron clusters are proposed as a new concept for the design of magnesium-battery electrolytes that are magnesium-battery-compatible, highly stable, and noncorrosive. A novel carborane-based electrolyte incorporating an unprecedented magnesium-centered complex anion is reported and shown to perform well as a magnesium-battery electrolyte. This finding opens a new approach towards the design of electrolytes whose likelihood of meeting the challenging design targets for magnesium-battery electro...

  1. Tri(ethylene glycol)-substituted trimethylsilane/lithium bis(oxalate)borate electrolyte for LiMn2O4/graphite system

    Science.gov (United States)

    Kusachi, Yuki; Dong, Jian; Zhang, Zhengcheng; Amine, Khalil

    2011-10-01

    Silane-based electrolyte is a promising candidate for safer electrochemical energy storage devices because it is thermally and electrochemical stable, less flammable and environmental benign. In this paper, electrochemical properties of one of the silane-based electrolytes, tri(ethylene glycol)-substituted trimethylsilane (1NM3)-lithium bis(oxalate)borate (LiBOB) was studied using LiMn2O4 as cathode and MAG graphite as anode. When combined with LiBOB as lithium salt, the 1NM3-LiBOB electrolyte can provide solid electrolyte interface (SEI) formation due to the reductive decomposition of LiBOB at first charging cycle. Compared to the electrolyte used in the conventional lithium-ion batteries, 1NM3-LiBOB electrolyte showed compatible battery performance in LiMn2O4/MAG chemistry. The AC impedance measurement indicates that the activation energy (Ea) obtained from the charge transfer impedance for 1NM3-LiBOB was higher than that of the state-of-the-art electrolyte. Due to its low conductivity, the rate capability of 1NM3-LiBOB electrolyte needs to be improved.

  2. Noise-based tube current reduction method with iterative reconstruction for reduction of radiation exposure in coronary CT angiography

    International Nuclear Information System (INIS)

    Purpose: To investigate the potential of noise-based tube current reduction method with iterative reconstruction to reduce radiation exposure while achieving consistent image quality in coronary CT angiography (CCTA). Materials and methods: 294 patients underwent CCTA on a 64-detector row CT equipped with iterative reconstruction. 102 patients with fixed tube current were assigned to Group 1, which was used to establish noise-based tube current modulation formulas, where tube current was modulated by the noise of test bolus image. 192 patients with noise-based tube current were randomly assigned to Group 2 and Group 3. Filtered back projection was applied for Group 2 and iterative reconstruction for Group 3. Qualitative image quality was assessed with a 5 point score. Image noise, signal intensity, volume CT dose index, and dose-length product were measured. Results: The noise-based tube current modulation formulas were established through regression analysis using image noise measurements in Group 1. Image noise was precisely maintained at the target value of 35.00 HU with small interquartile ranges for Group 2 (34.17–35.08 HU) and Group 3 (34.34–35.03 HU), while it was from 28.41 to 36.49 HU for Group 1. All images in the three groups were acceptable for diagnosis. A relative 14% and 41% reduction in effective dose for Group 2 and Group 3 were observed compared with Group 1. Conclusion: Adequate image quality could be maintained at a desired and consistent noise level with overall 14% dose reduction using noise-based tube current reduction method. The use of iterative reconstruction further achieved approximately 40% reduction in effective dose

  3. Surface characterization and corrosion behavior of calcium phosphate-base composite layer on titanium and its alloys via plasma electrolytic oxidation: A review paper.

    Science.gov (United States)

    Rafieerad, A R; Ashra, M R; Mahmoodian, R; Bushroa, A R

    2015-12-01

    In recent years, calcium phosphate-base composites, such as hydroxyapatite (HA) and carbonate apatite (CA) have been considered desirable and biocompatible coating layers in clinical and biomedical applications such as implants because of the high resistance of the composites. This review focuses on the effects of voltage, time and electrolytes on a calcium phosphate-base composite layer in case of pure titanium and other biomedical grade titanium alloys via the plasma electrolytic oxidation (PEO) method. Remarkably, these parameters changed the structure, morphology, pH, thickness and crystallinity of the obtained coating for various engineering and biomedical applications. Hence, the structured layer caused improvement of the biocompatibility, corrosion resistance and assignment of extra benefits for Osseo integration. The fabricated layer with a thickness range of 10 to 20 μm was evaluated for physical, chemical, mechanical and tribological characteristics via XRD, FESEM, EDS, EIS and corrosion analysis respectively, to determine the effects of the applied parameters and various electrolytes on morphology and phase transition. Moreover, it was observed that during PEO, the concentration of calcium, phosphor and titanium shifts upward, which leads to an enhanced bioactivity by altering the thickness. The results confirm that the crystallinity, thickness and contents of composite layer can be changed by applying thermal treatments. The corrosion behavior was investigated via the potentiodynamic polarization test in a body-simulated environment. Here, the optimum corrosion resistance was obtained for the coating process condition at 500 V for 15 min in Ringer solution. This review has been summarized, aiming at the further development of PEO by producing more adequate titanium-base implants along with desired mechanical and biomedical features.

  4. Electrolytes - Technology review

    Energy Technology Data Exchange (ETDEWEB)

    Meutzner, Falk; Ureña de Vivanco, Mateo [Institut für Experimentelle Physik, Technische Universität Bergakademie Freiberg, Leipziger Straße 23, 09596 Freiberg (Germany)

    2014-06-16

    Safety, lifetime, energy density, and costs are the key factors for battery development. This generates the need for improved cell chemistries and new, advanced battery materials. The components of an electrolyte are the solvent, in which a conducting salt and additives are dissolved. Each of them plays a specific role in the overall mechanism of a cell: the solvent provides the host medium for ionic conductivity, which originates in the conductive salt. Furthermore, additives can be used to optimize safety, performance, and cyclability. By understanding the tasks of the individual components and their optimum conditions of operation, the functionality of cells can be improved from a holistic point of view. This paper will present the most important technological features and requirements for electrolytes in lithium-ion batteries. The state-of-the-art chemistry of each component is presented, as well as different approaches for their modification. Finally, a comparison of Li-cells with lithium-based technologies currently under development is conducted.

  5. Electrolytes - Technology review

    International Nuclear Information System (INIS)

    Safety, lifetime, energy density, and costs are the key factors for battery development. This generates the need for improved cell chemistries and new, advanced battery materials. The components of an electrolyte are the solvent, in which a conducting salt and additives are dissolved. Each of them plays a specific role in the overall mechanism of a cell: the solvent provides the host medium for ionic conductivity, which originates in the conductive salt. Furthermore, additives can be used to optimize safety, performance, and cyclability. By understanding the tasks of the individual components and their optimum conditions of operation, the functionality of cells can be improved from a holistic point of view. This paper will present the most important technological features and requirements for electrolytes in lithium-ion batteries. The state-of-the-art chemistry of each component is presented, as well as different approaches for their modification. Finally, a comparison of Li-cells with lithium-based technologies currently under development is conducted

  6. 5 CFR 9901.343 - Pay reduction based on unacceptable performance and/or conduct.

    Science.gov (United States)

    2010-01-01

    ...) DEPARTMENT OF DEFENSE NATIONAL SECURITY PERSONNEL SYSTEM (NSPS) Pay and Pay Administration Performance-Based Pay § 9901.343 Pay reduction based on unacceptable performance and/or conduct. An employee's rate of... 5 Administrative Personnel 3 2010-01-01 2010-01-01 false Pay reduction based on...

  7. DOL/DME基LiTFSI电解液的离子传输性能%Ion transport property of LiTFSI electrolyte based on DOL/DME

    Institute of Scientific and Technical Information of China (English)

    熊仕昭; 谢凯; 洪晓斌

    2011-01-01

    用毛细管法、电导率测定等方法,测定了高浓度1,3-二氧戊环(DOL)/乙二醇二甲醚(DME)基二(三氟甲基磺酸)亚胺锂(LiTFSI)电解液的离子传输性能,以Eyring的传输过程模型和Jones-Dole方程,分别讨论了温度和锂盐浓度对黏度的影响,以修正的Casteel-Amis方程讨论了锂盐浓度对电导率的影响.3.0 mol/L LiTFSI/DOL+DME电解液粘性流动的活化能为10.64kJ/mol;当锂盐浓度大于1.50 mol/L时,DOL/DME基LiTFSI电解液的黏度会急剧上升;当锂盐质量摩尔浓度为1.50 mol/kg时,DOL/DME基LiTFSI电解液具有最高的电导率.%Ion transport property of concentrated 1,3-dioxolane(DOL)/dimethoxy ethane(DME) based LiN(CF3SO2)2 (LiTFSI) electrolyte was investigated by the methods of capillary and conductivity measuring. The effects of temperature and lithium salt concentration on the viscosity were discussed in term of Eyring's model for transport processes and the Jones-Dole equation. The effect of the salt concentration on the conductivity was discussed in term of the Casteel-Amis equation. The activation energy for the viscous flow of the 3.0 mol/L LiTFSI/DOL + DME electrolyte was 10.64 kJ/mol. Viscosity of the DOL/DME based LiTFSI electrolyte increased sharply when the concentration of lithium salt was more than 1.50 mol/L.The DOL/DME based LiTFSI electrolyte had the highest ionic conductivity when the molality of lithium salt was 1.50 mol/kg.

  8. Gel electrolyte for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen, Zonghai; Amine, K. [Chemical Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States); Zhang, L.Z.; West, R. [Organosilicon Research Center, Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706 (United States)

    2008-03-10

    The electrochemical performance of gel electrolytes based on crosslinked poly[ethyleneoxide-co-2-(2-methoxyethyoxy)ethyl glycidyl ether-co-allyl glycidyl ether] was investigated using graphite/Li{sub 1.1}[Ni{sub 1/3}Mn{sub 1/3}Co{sub 1/3}]{sub 0.9}O{sub 2} lithium-ion cells. It was found that the conductivity of the crosslinked gel electrolytes was as high as 5.9 mS/cm at room temperature, which is very similar to that of the conventional organic carbonate liquid electrolytes. Moreover, the capacity retention of lithium-ion cells comprising gel electrolytes was also similar to that of cells with conventional electrolytes. Despite of the high conductivity of the gel electrolytes, the rate capability of lithium-ion cells comprising gel electrolytes is inferior to that of the conventional cells. The difference was believed to be caused by the poor wettability of gel electrolytes on the electrode surfaces. (author)

  9. Gel electrolyte for lithium-ion batteries

    Energy Technology Data Exchange (ETDEWEB)

    Chen Zonghai [Chemical Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States); Zhang, L.Z.; West, R. [Organosilicon Research Center, Department of Chemistry, University of Wisconsin-Madison, 1101 University Avenue, Madison, WI 53706 (United States); Amine, K. [Chemical Engineering Division, Argonne National Laboratory, 9700 South Cass Avenue, Argonne, IL 60439 (United States)], E-mail: amine@cmt.anl.gov

    2008-03-10

    The electrochemical performance of gel electrolytes based on crosslinked poly[ethyleneoxide-co-2-(2-methoxyethyoxy)ethyl glycidyl ether-co-allyl glycidyl ether] was investigated using graphite/Li{sub 1.1}[Ni{sub 1/3}Mn{sub 1/3}Co{sub 1/3}]{sub 0.9}O{sub 2} lithium-ion cells. It was found that the conductivity of the crosslinked gel electrolytes was as high as 5.9 mS/cm at room temperature, which is very similar to that of the conventional organic carbonate liquid electrolytes. Moreover, the capacity retention of lithium-ion cells comprising gel electrolytes was also similar to that of cells with conventional electrolytes. Despite of the high conductivity of the gel electrolytes, the rate capability of lithium-ion cells comprising gel electrolytes is inferior to that of the conventional cells. The difference was believed to be caused by the poor wettability of gel electrolytes on the electrode surfaces.

  10. electrocatalytic nitrate reduction on palladium based catalysts activated with germanium

    NARCIS (Netherlands)

    Gootzen, J.F.E.; Lefferts, L.; Veen, van J.A.R.

    1999-01-01

    The electrocatalytic reduction of nitrate has been studied with electrochemical methods on palladium and palladium–platinum electrodes activated with germanium. The formation of a palladium–germanium alloy that occurs at germanium coverage above 0.2 has a strong enhancing effect on the rate of nitra

  11. Analysis of speckle reduction based on theory of optical eigenfunction

    Institute of Scientific and Technical Information of China (English)

    Gaoming Li; Shou Liu; Yishen Qiu; Hui Li; Yan Huang; Lijuan Wang

    2011-01-01

    The principle of optical eigenfunction is used in the analysis of speckle reduction in laser projection display.When the moving diffuser is used in the speckle reduction approach, the speckle contrast is decided by both the degree of freedom (DOF) of the projector and the area of resolving cell of the eyes on the screen. It can gain high DOF of the projector by increasing the space-bandwidth product, i.e., adopting a projection lens with a high numerical aperture or a large viewing field. The best scheme is equalizing the DOF of the scattering wave from a moving diffuser to that of the projection lens. The experimental results are in accordance with the conclusion drawn by optical eigenfunction.%@@ The principle of optical eigenfunction is used in the analysis of speckle reduction in laser projection display.When the moving diffuser is used in the speckle reduction approach, the speckle contrast is decided by both the degree of freedom (DOF) of the projector and the area of resolving cell of the eyes on the screen.It can gain high DOF of the projector by increasing the space-bandwidth product, i.e., adopting a projection lens with a high numerical aperture or a large viewing field.The best scheme is equalizing the DOF of the scattering wave from a moving diffuser to that of the projection lens.The experimental results are inaccordance with the conclusion drawn by optical eigenfunction.

  12. Speckle reduction methods in laser-based picture projectors

    Science.gov (United States)

    Akram, M. Nadeem; Chen, Xuyuan

    2016-02-01

    Laser sources have been promised for many years to be better light sources as compared to traditional lamps or light-emitting diodes (LEDs) for projectors, which enable projectors having wide colour gamut for vivid image, super brightness and high contrast for the best picture quality, long lifetime for maintain free operation, mercury free, and low power consumption for green environment. A major technology obstacle in using lasers for projection has been the speckle noise caused by to the coherent nature of the lasers. For speckle reduction, current state of the art solutions apply moving parts with large physical space demand. Solutions beyond the state of the art need to be developed such as integrated optical components, hybrid MOEMS devices, and active phase modulators for compact speckle reduction. In this article, major methods reported in the literature for the speckle reduction in laser projectors are presented and explained. With the advancement in semiconductor lasers with largely reduced cost for the red, green and the blue primary colours, and the developed methods for their speckle reduction, it is hoped that the lasers will be widely utilized in different projector applications in the near future.

  13. Defeaturing CAD models using a geometry-based size field and facet-based reduction operators.

    Energy Technology Data Exchange (ETDEWEB)

    Quadros, William Roshan; Owen, Steven James

    2010-04-01

    We propose a method to automatically defeature a CAD model by detecting irrelevant features using a geometry-based size field and a method to remove the irrelevant features via facet-based operations on a discrete representation. A discrete B-Rep model is first created by obtaining a faceted representation of the CAD entities. The candidate facet entities are then marked for reduction by using a geometry-based size field. This is accomplished by estimating local mesh sizes based on geometric criteria. If the field value at a facet entity goes below a user specified threshold value then it is identified as an irrelevant feature and is marked for reduction. The reduction of marked facet entities is primarily performed using an edge collapse operator. Care is taken to retain a valid geometry and topology of the discrete model throughout the procedure. The original model is not altered as the defeaturing is performed on a separate discrete model. Associativity between the entities of the discrete model and that of original CAD model is maintained in order to decode the attributes and boundary conditions applied on the original CAD entities onto the mesh via the entities of the discrete model. Example models are presented to illustrate the effectiveness of the proposed approach.

  14. The buffer effect in neutral electrolyte supercapacitors

    DEFF Research Database (Denmark)

    Thrane Vindt, Steffen; Skou, Eivind M.

    2016-01-01

    The observation that double-layer capacitors based on neutral aqueous electrolytes can have significantly wider usable potential windows than those based on acidic or alkaline electrolytes is studied. This effect is explained by a local pH change taking place at the electrode surfaces, leading...... to a change in the redox potential of water in opposite directions on the two electrodes, resulting in the wider stability window. The magnitude of this effect is suggested to be dependent on the buffer capacity, rather than the intrinsic pH value of the electrolyte. This is confirmed by studying the impact...

  15. Performance study of magnesium-sulfur battery using a graphene based sulfur composite cathode electrode and a non-nucleophilic Mg electrolyte

    Science.gov (United States)

    Vinayan, B. P.; Zhao-Karger, Zhirong; Diemant, Thomas; Chakravadhanula, Venkata Sai Kiran; Schwarzburger, Nele I.; Cambaz, Musa Ali; Behm, R. Jürgen; Kübel, Christian; Fichtner, Maximilian

    2016-02-01

    Here we report for the first time the development of a Mg rechargeable battery using a graphene-sulfur nanocomposite as the cathode, a Mg-carbon composite as the anode and a non-nucleophilic Mg based complex in tetraglyme solvent as the electrolyte. The graphene-sulfur nanocomposites are prepared through a new pathway by the combination of thermal and chemical precipitation methods. The Mg/S cell delivers a higher reversible capacity (448 mA h g-1), a longer cyclability (236 mA h g-1 at the end of the 50th cycle) and a better rate capability than previously described cells. The dissolution of Mg polysulfides to the anode side was studied by X-ray photoelectron spectroscopy. The use of a graphene-sulfur composite cathode electrode, with the properties of a high surface area, a porous morphology, a very good electronic conductivity and the presence of oxygen functional groups, along with a non-nucleophilic Mg electrolyte gives an improved battery performance.Here we report for the first time the development of a Mg rechargeable battery using a graphene-sulfur nanocomposite as the cathode, a Mg-carbon composite as the anode and a non-nucleophilic Mg based complex in tetraglyme solvent as the electrolyte. The graphene-sulfur nanocomposites are prepared through a new pathway by the combination of thermal and chemical precipitation methods. The Mg/S cell delivers a higher reversible capacity (448 mA h g-1), a longer cyclability (236 mA h g-1 at the end of the 50th cycle) and a better rate capability than previously described cells. The dissolution of Mg polysulfides to the anode side was studied by X-ray photoelectron spectroscopy. The use of a graphene-sulfur composite cathode electrode, with the properties of a high surface area, a porous morphology, a very good electronic conductivity and the presence of oxygen functional groups, along with a non-nucleophilic Mg electrolyte gives an improved battery performance. Electronic supplementary information (ESI) available

  16. Electrochemical characterization of MnO2-based composite in the presence of salt-in-water and water-in-salt electrolytes as electrode for electrochemical capacitors

    Science.gov (United States)

    Gambou-Bosca, Axel; Bélanger, Daniel

    2016-09-01

    The effect of the electrolyte on the electrochemical utilization of manganese dioxide as active material for electrochemical capacitor was studied by cyclic voltammetry and electrochemical impedance spectroscopy. MnO2-based composite electrodes were characterized in salt-in-water (0.65 M K2SO4, 5 M LiNO3, 0.5 M LiNO3 and 0.5 M Ca(NO3)2) and water-in-salt (5 M LiTFSI (lithium bis-trifluoromethanesulfonimide)) electrolytes. Firstly, no effect of the cation valence on the specific capacitance was observed as similar values were measured in 0.5 M LiNO3 and 0.5 M Ca(NO3)2 aqueous solutions at both low and high scan rate, when a MnO2-based composite electrode was cycled in the pseudocapacitive potential region. Secondly, it was found that in 5 M LiTFSI, a MnO2 electrode is characterized by an extended potential stability window of about 1.4 V and exhibits a high specific capacitance of 239 F g-1 per active material mass at a scan rate of 2 mV s-1. However due to the low ionic conductivity of this solution, the rate capability is limited at high scan rate.

  17. Properties of a ceria-based (C6S2G2 solid oxide electrolyte sintered with Al2O3 additive

    Directory of Open Access Journals (Sweden)

    Liu Y.H.

    2008-01-01

    Full Text Available Ceria-based Al2O3 composite electrolytes were prepared using (CeO20.6(SmO1.50.2(GdO1.50.2 (C6S2G2 and Al2O3 powders, employing sol-gel and low temperature combustion synthesis methods (SGLCS. The influence of Al2O3 content on the sintering behavior and electrical properties was studied. The results showed that electrical properties could be improved by adding 10wt% Al2O3. The sintered density was up to 5.61g/cm3. Most measurements of open circuit voltage (OCV ranged between 0.8 and 1.2V; an OCV value of 1.15V was obtained at 370oC. The performance of intermediate- temperature solid oxide fuel cells (ITSOFCs with a properly Al2O3 doped electrolyte was better than when a pure ceria-based one was used. The highest power density was 200mWcm-2.

  18. Attribute reduction theory of concept lattice based on decision formal contexts

    Institute of Scientific and Technical Information of China (English)

    WEI Ling; QI diandun; ZHANG WenXiu

    2008-01-01

    The theory of concept lattices is an efficient tool for knowledge representation and knowledge discovery,and is applied to many fields successfully.One focus of knowledge discovery is knowledge reduction.Based on the reduction theory of classical formal context,this paper proposes the definition of decision formal context and its reduction theory,which extends the reduction theory of concept lattices.In this paper,strong consistence and weak consistence of decision formal context are defined respectively.For strongly consistent decision formal context,the judgment theorems of consistent sets are examined,and approaches to reduc-tion are given.For weakly consistent decision formal context,implication mapping is defined,and its reduction is studied.Finally,the relation between reducts of weakly consistent decision formal context and reducts of implication mapping is discussed.

  19. Improved Durability of Electrocatalyst Based on Coating of Carbon Black with Polybenzimidazole and their Application in Polymer Electrolyte Fuel Cells.

    Science.gov (United States)

    Fujigaya, Tsuyohiko; Hirata, Shinsuke; Berber, Mohamed R; Nakashima, Naotoshi

    2016-06-15

    Improvement of durability of the electrocatalyst has been the key issue to be solved for the practical application of polymer electrolyte membrane fuel cells. One of the promising strategies to improve the durability is to enhance the oxidation stability of the carbon-supporting materials. In this report, we describe in detail the mechanism of the stability improvement of carbon blacks (CBs; Vulcan and Ketjen) by coating with polybenzimidazole (PBI). Nitrogen adsorption experiments reveal that the PBI coating of CBs results in the capping of the gates of the CB-micropores by the PBI. Since the surface of the micropores inside the CBs are inherently highly oxidized, the capping of such pores effectively prevents the penetration of the electrolyte into the pore and works to avoid the further oxidation of interior of the micropore, which is proved by cyclic voltammogram measurements. Above mechanism agrees very well with the dramatic enhancement of the durability of the membrane electrode assembly fabricated using Pt on the PBI-coated CBs as an electrocatalyst compared to the conventional Pt/CB (PBI-non coated) catalyst.

  20. High-performance flexible all-solid-state microbatteries based on solid electrolyte of lithium boron oxynitride

    Science.gov (United States)

    Song, Seung-Wan; Lee, Ki-Chang; Park, Ho-Young

    2016-10-01

    Rapidly growing interest and demand for wearable electronics require the development of flexible and lightweight all-solid-state batteries as power sources that guarantee high performance and safety with the absence of the risk of fire or explosion that can occur with traditional liquid electrolyte systems. Herein, we successfully fabricate new flexible all-solid-state microbatteries integrating a solid electrolyte film of lithium boron oxynitride (LiBON) on a flexible substrate using sophisticated thin-film fabrication technology. The new microbattery of Li/LiBON/LiCoO2 exhibits excellent mechanical integrity even under severe bending and twisting test conditions, enabling the realization of flexible microbatteries. The microbatteries demonstrate superior electrochemical cycling stability relative to conventional batteries, delivering an outstanding capacity retention of 90% on the 1000th cycle. Furthermore, operation at various temperatures from -10 °C to +60 °C and fast charging within 3-6 min are achieved. With various types of flexible substrates, the microbatteries can provide diverse opportunities for flexible and wearable electronics.

  1. Ionic Borate-Based Covalent Organic Frameworks: Lightweight Porous Materials for Lithium-Stable Solid State Electrolytes

    Energy Technology Data Exchange (ETDEWEB)

    Black, Hayden T; Harrison, Katharine Lee

    2016-10-01

    The synthesis and characterization of the first polyelectrolyte of intrinsic microporosity (PEIM) is described. The novel material was synthesized via reaction between the nitrile group in the polymer backbone and n-butyl lithium, effectively anchoring an imine anion to the porous framework while introducing a mobile lithium counterion. The PEIM was characterized by 13C, 1H, and 7Li NMR experiments, revealing quantitative conversion of the nitrile functionality to the anionic imine. Variable temperature 7Li NMR analysis of the dry PEIM and the electrolyteswollen PEIM revealed that lithium ion transport within the dry PEIM was largely due to interchain hopping of the Li+ ions, and that the mobility of polymer associated Li+ was reduced after swelling in electrolyte solution. Meanwhile, the swollen PEIM supported efficient transport of dissolved Li+ within the expanded pores. These results are discussed in the context of developing novel solid or solid-like lithium ion electrolytes using the new PEIM material.

  2. Dye-sensitized solar cell with poly(acrylic acid-co-acrylonitrile)-based gel polymer electrolyte

    International Nuclear Information System (INIS)

    Highlights: ► A nontoxic, easily synthesized poly(acrylic acid-co-acrylonitrile) showed suitable transmittance for dye-sensitized solar cell. ► A cell with relatively large active area fabricated with this polymer material showed acceptable efficiency. ► The gel polymer matrix affected the charge recombination, I3− diffusion, double layer capacitance, and electron lifetime in the cell. - Abstract: A non-conducting, nontoxic poly(acrylic acid-co-acrylonitrile) (PAA) was prepared and used as a supporting matrix for the electrolyte of dye-sensitized solar cells (DSSCs). DSSCs of active area 0.80 cm × 1.10 cm fabricated with PAA, 0.5 M LiI, 0.05 M I2, 0.5 M 3-tert-butylpyridine, and 0.1 M 1-methyl-3-propylimidazolium iodide in 3-methoxypropionitrile solvent showed an average solar energy conversion efficiency of 1.61% under simulated sunlight illumination of 100 mW cm−2, AM 1.5. The effects of the gel polymer matrix on the electrochemical properties of DSSCs were studied using the electrochemical impedance spectroscopy. Relative to the non-gel reference cells, the results showed a decrease in charge recombination, ionic diffusion, and double layer capacitance and an increase in electron lifetime. These results could play an important role in determining the future direction for the development of high-performance gel polymer electrolytes.

  3. Autogenous electrolyte, non-pyrolytically produced solid capacitor structure

    Science.gov (United States)

    Sharp, D.J.; Armstrong, P.S.; Panitz, J.K.G.

    1998-03-17

    A solid electrolytic capacitor is described having a solid electrolyte comprising manganese dioxide dispersed in an aromatic polyamide capable of further cure to form polyimide linkages, the solid electrolyte being disposed between a first electrode made of valve metal covered by an anodic oxide film and a second electrode opposite the first electrode. The electrolyte autogenously produces water, oxygen, and hydroxyl groups which act as healing substances and is not itself produced pyrolytically. Reduction of the manganese dioxide and the water molecules released by formation of imide linkages result in substantially improved self-healing of anodic dielectric layer defects. 2 figs.

  4. Rough Set Based K-Exception Approach to Approximate Rule Reduction

    Institute of Scientific and Technical Information of China (English)

    ZHANG Feng; ZHANG Xianfeng; QIN Zhiguang; LIU Jinde

    2003-01-01

    There are rules refering to infrequent instances after the procession of attribute reduction and value reduction with traditional methods. A rough set RS based k-exception approach (RSKEA) to rule reduction is presented. Its main idea lies in a two-phase RS based rule reduction. An ordinary decision table is attained through general method of RS knowledge reduction in the first phase. Then a kexception candidate set is nominated according to the decision table. RS rule reduction is employed for the reformed source data set, which remove all the instances included in the k-exception set. We apply the approach to the automobile database. Results show that it can reduce the number and complexity of rules with adjustable conflict rate, which contributes to approximate rule reduction.

  5. Preparation of micron-sized Li{sub 4}Ti{sub 5}O{sub 12} and its electrochemistry in polyacrylonitrile electrolyte-based lithium cells

    Energy Technology Data Exchange (ETDEWEB)

    Peramunage, D.; Abraham, K.M. [EIC Labs., Inc., Norwood, MA (United States)

    1998-08-01

    Micron-sized Li{sub 4}Ti{sub 5}O{sub 12} was prepared in a single-step solid-state reaction involving TiO{sub 2} and Li{sub 2}CO{sub 3}, and its electrochemical behavior was evaluated in Li and Li-ion cells containing a polyacrylonitrile (PAN)-based solid polymer electrolyte. The usefulness of Li{sub 4}Ti{sub 5}O{sub 12} was demonstrated for three distinctive applications: (1) cathode of a 1.5 V rechargeable Li battery, (2) auxiliary electrode for investigating the electrochemistry of Li insertion cathode materials, and (3) anode of a Li-ion cell in conjunction with a high voltage cathode, e.g., cubic spinel LiMn{sub 2}O{sub 4}. The micron-sized Li{sub 4}Ti{sub 5}O{sub 12} exhibited a capacity of 160 mAh/g at C/20--C/30 rates which about 7% better than the capacity exhibited by this material prepared according to a previously published procedure. More importantly, the micron-sized oxide showed significantly better high rate capability, yielding 25--50% larger capacity at the 3C to 8C rates. Li//solid polymer electrolyte//Li{sub 4}Ti{sub 5}O{sub 12} cells underwent extended, full-depth, charge/discharge cycling at {ge}1C rates with virtually no capacity fade. The auxiliary electrode concept was demonstrated in Li{sub (4+x)}Ti{sub 5}O{sub 12} (x {approximately} 1.2)//solid polymer electrolyte//LiMn{sub 2}O{sub 4} cells. At a 1C discharge rate, more than 150 cycles were demonstrated in these cells with a capacity fade rate of about 0.1% per cycle and an end utilization of {approximately}90 mAh/g for spinel LiMn{sub 2}O{sub 4}. Balanced Li{sub 4}Ti{sub 5}O{sub 12}//solid polymer electrolyte//LiMn{sub 2}O{sub 4} cells of slightly cathode-limited configuration showed full-depth extended cycling capability at a utilization of {approximately}90 mAh/g for LiMn{sub 2}O{sub 4} at 1C rate and a capacity fade rate of about 0.08% per cycle.

  6. Towards Li(Ni0.33Mn0.33Co0.33)O2/graphite batteries with ionic liquid-based electrolytes. I. Electrodes' behavior in lithium half-cells

    Science.gov (United States)

    Simonetti, E.; Maresca, G.; Appetecchi, G. B.; Kim, G.-T.; Loeffler, N.; Passerini, S.

    2016-11-01

    Lithium cells based on NMC cathodes or graphite anodes and ionic liquid-based electrolyte mixtures are investigated. The electrode tapes, using water-soluble natural binders, as well as the ionic liquid materials, are prepared through eco-friendly routes involving H2O as the only processing solvent. The Li/NMC and Li/graphite half-cells are studied by cyclic voltammetry, impedance spectroscopy and galvanostatic cycling tests at different temperatures. The results herein reported, demonstrate the performance improvement in terms of cycling behavior and ageing resistance, granted by the ionic liquid mixtures with respect to the electrolytes reported in literature based on a single ionic liquid.

  7. Mindfulness-based stress reduction: Does mindfulness training affect competence based self-esteem and burnout?

    OpenAIRE

    Rajamäki, Suvi

    2011-01-01

    Competence based self-esteem (CBSE) refers to a disposition where an individual strives for self-worth by achievements to compensate a low basic self-esteem (BSE). This kind of self-attitude is linked to burnout. The purpose of the study was to examine the effects of an 8-week mindfulness based stress reduction (MBSR) intervention on self-ratings of CBSE, BSE, burnout and mindfulness. Four MBSR groups were enrolled and a total sample comprised 29 participants. Results of repeated measures ANO...

  8. 碱性介质中Fe/N/C催化剂的氧气还原反应催化性能研究%Electrocatalytic Activity of Fe/N/C Catalyst for the Oxygen Reduction Reaction in Alkaline Electrolyte

    Institute of Scientific and Technical Information of China (English)

    郑龙珍; 陶堃; 熊乐艳; 叶丹; 韩奎; 纪忆

    2012-01-01

    以氧化石墨烯(GO)为碳载体,K3Fe(CN)6同时作为N源和Fe源,经热处理后构建了新型Fe/N/C结构的氧气还原催化剂.在热处理过程中,氧化石墨烯上的官能团分解脱离形成活性中心,Fe元素和N元素的同时掺杂是通过氧化石墨烯与K3Fe(CN)6之间的相互作用而实现的.通过傅立叶变换红外光谱(FTIR)和X射线光电子能谱(XPS)表征证明了这种非贵金属催化剂中N元素和Fe元素的成功掺杂,在催化剂中N元素主要是以吡啶式氮、吡咯式氮和石墨式氮的形式存在,Fe(II)和Fe(III)则与其中的吡啶式氮配位形成Fe-Nx结构.采用循环伏安法(CV)和旋转圆盘电极(RDE)技术,研究其在碱性介质中对氧气还原反应(ORR)的电催化性能.实验结果显示:Fe/N/C催化剂具有良好的ORR电催化活性,在碱性溶液中的起始电位为-0.15 V,同时有着良好的稳定性和抗甲醇性能.%Fuel cells have been recognized as one of the most promising power sources due to their high efficiency and low emissions.However,the high cost and scarcity of traditional Pt-based catalyst limit their commercialization.More intensive research have been focused on the development of non-noble-metal catalysts in order to replace Pt for catalyzing oxygen reduction reaction(ORR).Recently,it was reported that the Fe/N/C catalyst have high activity toward ORR.Chemical vapor deposition(CVD) is the most common method for the preparation of the Fe/N/C catalyst.However,the cost of CVD method is much higher.Here we report a facile method for the preparation of Fe/N/C catalyst for ORR in alkaline electrolyte.The catalyst is prepared by using graphene oxide as carbon support,and K3Fe(CN)6 as both nitrogen and iron sources.The precursors are then treated thermally at 800 ℃ under nitrogen atmosphere.In the process of heat treatment,the functional groups of graphene oxide are decomposed to form active center.Simultaneous doping of N

  9. Preparation of novel carbon microfiber/carbon nanofiber-dispersed polyvinyl alcohol-based nanocomposite material for lithium-ion electrolyte battery separator.

    Science.gov (United States)

    Sharma, Ajit K; Khare, Prateek; Singh, Jayant K; Verma, Nishith

    2013-04-01

    A novel nanocomposite polyvinyl alcohol precursor-based material dispersed with the web of carbon microfibers and carbon nanofibers is developed as lithium (Li)-ion electrolyte battery separator. The primary synthesis steps of the separator material consist of esterification of polyvinyl acetate to produce polyvinyl alcohol gel, ball-milling of the surfactant dispersed carbon micro-nanofibers, mixing of the milled micron size (~500 nm) fibers to the reactant mixture at the incipience of the polyvinyl alcohol gel formation, and the mixing of hydrophobic reagents along with polyethylene glycol as a plasticizer, to produce a thin film of ~25 μm. The produced film, uniformly dispersed with carbon micro-nanofibers, has dramatically improved performance as a battery separator, with the ion conductivity of the electrolytes (LiPF6) saturated film measured as 0.119 S-cm(-1), approximately two orders of magnitude higher than that of polyvinyl alcohol. The other primary characteristics of the produced film, such as tensile strength, contact angle, and thermal stability, are also found to be superior to the materials made of other precursors, including polypropylene and polyethylene, discussed in the literature. The method of producing the films in this study is novel, simple, environmentally benign, and economically viable.

  10. Foil-based TiO2/gel electrolyte/Ni1-xO electrochromic device made of electrochromic pigment coatings.

    Science.gov (United States)

    Mihelčič, Mohor; Šurca-Vuk, Angela; Vrhovšk, Dejan; Švegl, Franc; Hajzeri, Metka; Orel, Boris

    2014-01-01

    Thin electrochromic coatings were obtained by co-grinding the mTiA particle aggregates (300 nm in size) with open-corner heptaisobutyl trisilanol POSS (T(8) IB(7)(OH)(3) POSS) acting as dispersant. After the addition of titanium tetraisopropoxide (3-5%) the mTiA pigment dispersion was deposited on FTO glass and plastic ITO PET foils and coatings were obtained by thermal treatment at 150 °C. Optical transmittance and luminous haze from 2 to 6% of the coatings were determined from the corresponding UV-Vis spectra. The achieved electrochromic effect was evaluated by electrochemical charging/discharging in 1 M LiClO(4)/PC electrolyte. Results revealed that the colouring/bleaching changes depended on the extent of grinding and the size of the milling zirconia beads, enabling to distinguish between the surface charging of the mTiA grains and the filling and emptying of the anatase density of states. mTiA pigment coatings deposited on plastic foil were used in combination with Ni(1-x)O pigment coatings for construction of foil-based electrochromic device employing novel gel electrolyte with ionic liquid co-solvent. PMID:25286207

  11. Effects of some rare earth and carbonate-based co-dopants on structural and electrical properties of samarium doped ceria (SDC) electrolytes for solid oxide fuel cells

    Science.gov (United States)

    Anwar, Mustafa; Khan, Zuhair S.; Mustafa, Kamal; Rana, Akmal

    2015-09-01

    In the present study, samarium doped ceria (SDC) and SDC-based composite with the addition of K2CO3 were prepared by co-precipitation route and effects of pH of the solution and calcination temperature on microstructure of SDC and SDC-K2CO3, respectively, were investigated. Furthermore, experimentation was performed to investigate into the ionic conductivity of pure SDC by co-doping with yttrium i.e., YSDC, XRD and SEM studies show that the crystallite size and particle size of SDC increases with the increase in pH. The SEM images of all the samples of SDC synthesized at different pH values showed the irregular shaped and dispersed particles. SDC-K2CO3 was calcined at 600∘C, 700∘C and 800∘C for 4 h and XRD results showed that crystallite size increases while lattice strain, decreases with the increase in calcination temperature and no peaks were detected for K2CO3 as it is present in an amorphous form. The ionic conductivity of the electrolytes increases with the increase in temperature and SDC-K2CO3 shows the highest value of ionic conductivity as compared to SDC and YSDC. Chemical compatibility tests were performed between the co-doped electrolyte and lithiated NiO cathode at high temperature. It revealed that the couple could be used up to the temperature of 700∘C.

  12. Synthesis, Multinuclear NMR Characterization and Dynamic Property of Organic–Inorganic Hybrid Electrolyte Membrane Based on Alkoxysilane and Poly(oxyalkylene Diamine

    Directory of Open Access Journals (Sweden)

    Hsien-Ming Kao

    2012-06-01

    Full Text Available Organic–inorganic hybrid electrolyte membranes based on poly(propylene glycol-block-poly(ethylene glycol-block-poly(propylene glycol bis(2-aminopropyl ether complexed with LiClO4 via the co-condensation of tetraethoxysilane (TEOS and 3-(triethoxysilylpropyl isocyanate have been prepared and characterized. A variety of techniques such as differential scanning calorimetry (DSC, Fourier transform infrared (FTIR spectroscopy, alternating current (AC impedance and solid-state nuclear magnetic resonance (NMR spectroscopy are performed to elucidate the relationship between the structural and dynamic properties of the hybrid electrolyte and the ion mobility. A VTF (Vogel-Tamman-Fulcher-like temperature dependence of ionic conductivity is observed for all the compositions studied, implying that the diffusion of charge carriers is assisted by the segmental motions of the polymer chains. A maximum ionic conductivity value of 5.3 × 10−5 Scm−1 is obtained at 30 °C. Solid-state NMR results provide a microscopic view of the effects of salt concentrations on the dynamic behavior of the polymer chains.

  13. Synthesis, Multinuclear NMR Characterization and Dynamic Property of Organic–Inorganic Hybrid Electrolyte Membrane Based on Alkoxysilane and Poly(oxyalkylene) Diamine

    Science.gov (United States)

    Saikia, Diganta; Pan, Yu-Chi; Kao, Hsien-Ming

    2012-01-01

    Organic–inorganic hybrid electrolyte membranes based on poly(propylene glycol)-block-poly(ethylene glycol)-block-poly(propylene glycol) bis(2-aminopropyl ether) complexed with LiClO4 via the co-condensation of tetraethoxysilane (TEOS) and 3-(triethoxysilyl)propyl isocyanate have been prepared and characterized. A variety of techniques such as differential scanning calorimetry (DSC), Fourier transform infrared (FTIR) spectroscopy, alternating current (AC) impedance and solid-state nuclear magnetic resonance (NMR) spectroscopy are performed to elucidate the relationship between the structural and dynamic properties of the hybrid electrolyte and the ion mobility. A VTF (Vogel-Tamman-Fulcher)-like temperature dependence of ionic conductivity is observed for all the compositions studied, implying that the diffusion of charge carriers is assisted by the segmental motions of the polymer chains. A maximum ionic conductivity value of 5.3 × 10−5 Scm−1 is obtained at 30 °C. Solid-state NMR results provide a microscopic view of the effects of salt concentrations on the dynamic behavior of the polymer chains. PMID:24958176

  14. Infrared studies of polyacrylonitrile-based polymer electrolytes incorporated with lithium bis(trifluoromethane)sulfonimide and urea as deep eutectic solvent

    Science.gov (United States)

    Sim, L. N.; Yahya, R.; Arof, A. K.

    2016-06-01

    In this work, urea is introduced into polyacrylonitrile (PAN)-based polymer electrolyte containing lithium bis(trifluoromethane)sulfonimide (LiTFSI) to form a deep eutectic solvent with urea and LiTFSI in the mole ratio of 1:3. The ambient ionic conductivity of the polymer electrolyte film is enhanced from 2.54 × 10-4 S cm-1 to 3.82 × 10-3 S cm-1 with the addition of urea. Infrared studies has revealed that urea interacts with the LiTFSI through coordination of Li+ ions onto the carbonyl (Cdbnd O) group of urea, and hydrogen bonding possibly to the O atoms in the SO2 groups of TFSI- ions. Hydrogen bonding interactions of urea with DMF and PAN are also evident. The enhancement in conductivity is believed to be due to urea being involved in the dissociation of LiTFSI and its role as an additional ion conduction pathway through its carbonyl group.

  15. SiNWs-based electrochemical double layer micro-supercapacitors with wide voltage window (4 V) and long cycling stability using a protic ionic liquid electrolyte

    Science.gov (United States)

    Aradilla, David; Gentile, Pascal; Ruiz, Vanesa; Gómez-Romero, Pedro; Wimberg, Jan; Iliev, Boyan; Schubert, Thomas J. S.; Sadki, Saïd; Bidan, Gérard

    2015-03-01

    The present work reports the use and application of a novel protic ionic liquid (triethylammonium bis(trifluoromethylsulfonyl)imide; NEt3H TFSI) as an electrolyte for symmetric planar micro-supercapacitors based on silicon nanowire electrodes. The excellent performance of the device has been successfully demonstrated using cyclic voltammetry, galvanostatic charge-discharge cycles and electrochemical impedance spectroscopy. The electrochemical characterization of this system exhibits a wide operative voltage of 4 V as well as an outstanding long cycling stability after millions of galvanostatic cycles at a high current density of 2 mA cm-2. In addition, the electrochemical double layer micro-supercapacitor was able to deliver a high power density of 4 mW cm-2 in a very short time pulses (a few ms). Our results could be of interest to develop prospective on-chip micro-supercapacitors using protic ionic liquids as electrolytes with high performance in terms of power and energy densities. Invited talk at the 2nd International Workshop on Nano Materials for Energy Conversion NMEC-2, 17-20 November, 2014, Ho Chi Minh City, Vietnam.

  16. Single-Ion-Conducting Nanocomposite Polymer Electrolytes for Lithium Batteries Based on Lithiated-Fluorinated-Iron Oxide and Poly(ethylene glycol) 400

    International Nuclear Information System (INIS)

    Highlights: • A family of nanocomposite polymer electrolytes (nCPEs) is prepared and characterized. • nCPEs consist of lithiated fluorinated iron oxide particles dispersed in PEG400. • The thermal properties, structure and electrical response of nCPEs are elucidated. • nCPEs are single-ion conductors with a high thermal stability and conductivity. - Abstract: A poly(ethylene glycol) 400 (PEG400) matrix doped with different amounts of a fluorinated Fe2O3-based nanofiller (LiFI) featuring a Li+-functionalised surface gives rise to nanocomposite polymer electrolytes (nCPEs) that demonstrate single-ion conduction. A family of nCPEs with general formula [PEG400/(LiFI)y] and y = nFe/nPEG400 ranging from 0 to 8.15 are prepared; they are characterized by Inductively Coupled Plasma Atomic Emission Spectroscopy (ICP-AES), High-Resolution Thermogravimetric Analysis (HR-TGA), Differential Scanning Calorimetry (DSC), and Fourier-transform vibrational spectroscopy in both the medium (MIR) and far (FIR) infrared. The Li+ transference number, tLi+,is determined and Broadband Electrical Spectroscopy (BES) is used to elucidate the electrical response of the materials in terms of polarization and relaxation events. The combination of the information obtained by all the aforementioned techniques enables us to present a possible conduction mechanism for these nCPEs single-ion conducting systems

  17. Approximation of skewed interfaces with tensor-based model reduction procedures: Application to the reduced basis hierarchical model reduction approach

    Science.gov (United States)

    Ohlberger, Mario; Smetana, Kathrin

    2016-09-01

    In this article we introduce a procedure, which allows to recover the potentially very good approximation properties of tensor-based model reduction procedures for the solution of partial differential equations in the presence of interfaces or strong gradients in the solution which are skewed with respect to the coordinate axes. The two key ideas are the location of the interface either by solving a lower-dimensional partial differential equation or by using data functions and the subsequent removal of the interface of the solution by choosing the determined interface as the lifting function of the Dirichlet boundary conditions. We demonstrate in numerical experiments for linear elliptic equations and the reduced basis-hierarchical model reduction approach that the proposed procedure locates the interface well and yields a significantly improved convergence behavior even in the case when we only consider an approximation of the interface.

  18. Towards Prognostics of Electrolytic Capacitors

    Data.gov (United States)

    National Aeronautics and Space Administration — A remaining useful life prediction algorithm and degradation model for electrolytic capacitors is presented. Electrolytic capacitors are used in several...

  19. LITHIUM ION CONDUCTING POLYMER ELECTROLYTES BASED ON ALTERNATING MALEIC ANHYDRIDE COPOLYMER WITH OLIGO-OXYETHYLENE SIDE CHAINS

    Institute of Scientific and Technical Information of China (English)

    DING Liming

    1996-01-01

    A comb polymer with oligo-oxyethylene side chains of the type -(CH2CH2O)12CH3 was prepared from methyl vinyl ether/maleic anhydride copolymer and poly (ethylene glycol) methyl ether. The polymer can dissolve LiClO4 salt to form homogeneous amorphous polymer electrolyte. The ac ion conduction was measured using the complex impedance method, and conductivities were investigated as functions of temperatures and salt concentration. The complexes were first found to have two classes of glass transition which increase with increasing salt content. The optimum conductivity attained at 25℃ is in the order of 5.50 × 10-6Scm-1. IR spectroscopy was used to study the cation-polymer interaction.

  20. Novel Proton Conducting Solid Bio-polymer Electrolytes Based on Carboxymethyl Cellulose Doped with Oleic Acid and Plasticized with Glycerol

    Science.gov (United States)

    Chai, M. N.; Isa, M. I. N.

    2016-01-01

    The plasticized solid bio-polymer electrolytes (SBEs) system has been formed by introducing glycerol (Gly) as the plasticizer into the carboxymethyl cellulose (CMC) doped with oleic acid (OA) via solution casting techniques. The ionic conductivity of the plasticized SBEs has been studied using Electrical Impedance Spectroscopy. The highest conductivity achieved is 1.64 × 10−4 S cm−1 for system containing 40 wt. % of glycerol. FTIR deconvolution technique had shown that the conductivity of CMC-OA-Gly SBEs is primarily influenced by the number density of mobile ions. Transference number measurement has shown that the cation diffusion coefficient and ionic mobility is higher than anion which proved the plasticized polymer system is a proton conductor. PMID:27265642