65 research outputs found

    Polypyrrole-Fe2O3 nanohybrid materials for electrochemical storage

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    We report on the synthesis and electrochemical characterization of nanohybrid polypyrrole (PPy) (PPy/Fe2O3) materials for electrochemical storage applications. We have shown that the incorporation of nanoparticles inside the PPy notably increases the charge storage capability in comparison to the “pure” conducting polymer. Incorporation of large anions, i.e., paratoluenesulfonate, allows a further improvement in the capacity. These charge storage modifications have been attributed to the morphology of the composite in which the particle sizes and the specific surface area are modified with the incorporation of nanoparticles. High capacity and stability have been obtained in PC/NEt4BF4 (at 20 mV/s), i.e., 47 mAh/g, with only a 3% charge loss after one thousand cyles. The kinetics of charge–discharge is also improved by the hybrid nanocomposite morphology modifications, which increase the rate of insertion–expulsion of counter anions in the bulk of the film. A room temperature ionic liquid such as imidazolium trifluoromethanesulfonimide seems to be a promising electrolyte because it further increases the capacity up to 53 mAh/g with a high stability during charge–discharge processes

    Maternal Serologic Screening to Prevent Congenital Toxoplasmosis: A Decision-Analytic Economic Model

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    We constructed a decision-analytic and cost-minimization model to compare monthly maternal serological screening for congenital toxoplasmosis, prenatal treatment, and post-natal follow-up and treatment according to the current French protocol, versus no systematic screening or perinatal treatment. Costs are based on published estimates of lifetime societal costs of developmental disabilities and current diagnostic and treatment costs. Probabilities are based on published results and clinical practice in the United States and France. We use sensitivity analysis to evaluate robustness of results. We find that universal monthly maternal screening for congenital toxoplasmosis with follow-up and treatment, following the French (Paris) protocol, leads to savings of 620perchildscreened.Resultsarerobusttochangesintestcosts,valueofstatisticallife,seroprevalenceinwomenofchildbearingage,fetallossduetoamniocentesis,incidenceofprimaryT.gondiiinfectionduringpregnancy,andtobivariateanalysisoftestcostsandincidenceofprimaryT.gondiiinfection.Giventheparametersinthismodelandamaternalscreeningtestcostof620 per child screened. Results are robust to changes in test costs, value of statistical life, seroprevalence in women of childbearing age, fetal loss due to amniocentesis, incidence of primary T. gondii infection during pregnancy, and to bivariate analysis of test costs and incidence of primary T. gondii infection. Given the parameters in this model and a maternal screening test cost of 12, screening is cost-saving for rates of congenital infection above 1 per 10,000 live births. Universal screening according to the French protocol is cost saving for the US population within broad parameters for costs and probabilities

    Ionic liquids at electrified interfaces

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    Until recently, “room-temperature” (<100–150 °C) liquid-state electrochemistry was mostly electrochemistry of diluted electrolytes(1)–(4) where dissolved salt ions were surrounded by a considerable amount of solvent molecules. Highly concentrated liquid electrolytes were mostly considered in the narrow (albeit important) niche of high-temperature electrochemistry of molten inorganic salts(5-9) and in the even narrower niche of “first-generation” room temperature ionic liquids, RTILs (such as chloro-aluminates and alkylammonium nitrates).(10-14) The situation has changed dramatically in the 2000s after the discovery of new moisture- and temperature-stable RTILs.(15, 16) These days, the “later generation” RTILs attracted wide attention within the electrochemical community.(17-31) Indeed, RTILs, as a class of compounds, possess a unique combination of properties (high charge density, electrochemical stability, low/negligible volatility, tunable polarity, etc.) that make them very attractive substances from fundamental and application points of view.(32-38) Most importantly, they can mix with each other in “cocktails” of one’s choice to acquire the desired properties (e.g., wider temperature range of the liquid phase(39, 40)) and can serve as almost “universal” solvents.(37, 41, 42) It is worth noting here one of the advantages of RTILs as compared to their high-temperature molten salt (HTMS)(43) “sister-systems”.(44) In RTILs the dissolved molecules are not imbedded in a harsh high temperature environment which could be destructive for many classes of fragile (organic) molecules

    Tuning the surface chemistry of mxene to improve energy storage : example of nitrification by salt melt

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    The unique properties of 2D MXenes, such as metal-like electrical conductivity and versatile surface chemistry, make them appealing for various applications, including energy storage. While surface terminations of 2D MXene are expected to have a key influence on their electrochemical properties, the conventional HF-etching method limits the surface functional groups to —F, —OH, and —O. In this study, O-free, Cl-terminated MXenes (noted as Ti3C2Clx) are first synthesized by a molten salt (FeCl2) etching route. Then, a substitution of surface termination from Cl— to N— is performed via post-thermal treatment of Ti3C2Clx in Li3N containing molten salt electrolytes. While the Cl-terminated pristine material does not show electrochemical activity, the surface-modified, N-containing Ti3C2Tx exhibits a unique capacitive-like electrochemical signature in sulfuric acid aqueous electrolyte with rate performance—more than 300 F g-1 (84 mAh g-1) at 2 V s-1. These results show that control of the MXene surface chemistry enables the preparation of high-performance electrodes in a previously not accessed limit of energy storage

    Capacitive deionization concept based on suspension electrodes without ion exchange membranes

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    A new type of capacitive deionization (CDI) system, based on capacitive suspension electrodes (CSEs), was developed for the purpose of desalting brackish and seawater through the use of flowable carbon suspensions. CSEs derived from activated carbon and acetylene black demonstrated a specific capacitance of 92 F g−1 in a static mode in a 0.6 M NaCl solution. The novel system introduced here is a proof of concept that capacitive suspension electrodes can be envisioned to desalt water without the aid of ion exchange membranes (IEMs). Keywords: Capacitive deionization, Capacitive suspension electrodes, Water desalination, Electrochemical flow capacitor, Flowable electrode
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