Abstract: Provided herein is a redox flow battery comprising an anode comprising anodic redox mediators; a negative electrolyte tank comprising an anolyte; and an anode pump capable of circulating the anolyte through the anode. The redox flow battery further comprises a cathode comprising cathodic redox mediators; a positive electrolyte tank comprising a catholyte and a cathode pump capable of circulating the catholyte through the cathode. A separator is between the anode and cathode.

Abstract: Provided is a device and a method for forming a metal plating film having a thick film thickness by a solid substitution-type electroless plating method. The present disclosure relates to a film formation device for forming a film of a first metal on a plating film of a second metal by a solid substitution-type electroless plating method, comprising: a conductive mounting base; a third metal; an insulating material; a microporous membrane; a plating bath chamber; and a pressing unit, wherein the third metal has an ionization tendency larger than ionization tendencies of the first metal and the second metal, and wherein the insulating material is installed between a base material and the third metal so as to contact respective materials of the base material and the third metal when the base material having the plating film of the second metal is installed.

Abstract: A membrane electrode assembly comprises an anode electrode comprising an anode catalyst layer and an anode gas diffusion layer, a cathode electrode comprising a cathode catalyst layer and a cathode gas diffusion layer, a polymer electrolyte membrane interposed between the anode catalyst layer and the cathode catalyst layer, and a layer comprising a fluoroalkyl-phosphonic acid compound between at least one of the anode gas diffusion layer and the anode catalyst layer, the anode catalyst layer and the polymer electrolyte membrane, the polymer electrolyte membrane and the cathode catalyst layer, and the cathode catalyst layer and the cathode gas diffusion layer.

Abstract: Method and apparatus for a low maintenance, high reliability on-site electrolytic generator incorporating automatic cell monitoring for contaminant film buildup, as well as automatically removing or cleaning the contaminant film. This method and apparatus preferably does not require human intervention to clean. For high current density cells, cleaning is preferably performed by reversing the polarity of the electrodes and applying a lower current density to the electrodes, preferably by adjusting the salinity or brine concentration of the electrolyte while keeping the voltage constant. Electrolyte flow preferably comprises water and brine flows which are preferably separately monitored and automatically adjusted. For bipolar cells, flow between modules arranged in parallel is preferably approximately equally distributed between modules and between intermediate electrodes within each module.

Abstract: Redox flow battery performance may be improved with a metal containing ionic liquid as a liquid electrolyte. Metal containing ionic liquids are liquids at all temperatures of interest and therefore do not need dilution. As such, voltage separation between the anolyte and catholyte may exceed 0.5 V and therefor rival current state-of-the-art energy storage technologies and with higher voltage separation may attain energy densities above 100 Wh/L.

Abstract: The present disclosure provides a flow battery comprising a flexible lithium ion conductive film having durability against a highly reductive non-aqueous electrolyte liquid. The flow battery according to the present disclosure comprises a first non-aqueous electrolyte liquid, a first electrode, a second electrode, and a lithium ion conductive film. The first non-aqueous electrolyte liquid contains lithium ions and further biphenyl, phenanthrene, stilbene, triphenylene, anthracene, acenaphthene, acenaphthylene, fluorene, fluoranthene, o-terphenyl, m-terphenyl, or p-terphenyl. The lithium ion conductive film comprises a composite body. The composite body contains a lithium ion conductive polymer and polyvinylidene fluoride. The lithium ion conductive polymer includes an aromatic ring into which a lithium salt of an acidic group has been introduced. The lithium ion conductive polymer and the polyvinylidene fluoride have been mixed with each other homogeneously in the composite body.

Abstract: A multi-cell battery system is disclosed including a plurality of battery sub-assemblies and a plurality of heat exchange members stacked together along a longitudinal axis. Each of the plurality of heat exchange members defines a heat exchange passageway through the battery system.

Abstract: A catalyst and a catalyst composition, a method for preparing thereof, and a method for synthesizing of hydrogen peroxide using them are provided. The catalyst and the catalyst composition contains: an alloy of two elements, wherein the elements are Pt (Platinum) and Ni (Nickel). The present disclosure enables (a) replacing a high-priced palladium (Pd) catalyst with a new catalyst, (b) providing a high-active catalyst which catalyzes the direct synthesis reaction of the hydrogen peroxide.

Abstract: Anode half-cells for the electrocatalytic oxidation of a liquid or gaseous fuel or other reductant are disclosed, along with electrochemical cells that include such half-cells. The anode half-cells include redox mediator/heterogeneous redox catalyst pairs within an electrolyte solution that is also in contact with an electrode. The electrode is not in direct contact with the heterogeneous catalyst. The redox mediator must include at least one carbon atom and be capable of transferring or accepting electrons and protons while undergoing reduction or oxidation. In operation, the fuel or other reductant is oxidized and the redox mediator is reduced at the heterogeneous catalyst. The reduced form of the redox mediator can then migrate to the electrode, where it is converted back to its oxidized form, which can then migrate back to the heterogeneous catalyst, where the cycle is repeated.

Abstract: A redox flow battery includes a battery cell including a positive electrode, a negative electrode, and a membrane disposed between these two electrodes; a positive electrode electrolyte supplied to the positive electrode; and a negative electrode electrolyte supplied to the negative electrode, wherein the positive electrode electrolyte contains manganese ions and a phosphorus-containing substance, the negative electrode electrolyte contains at least one species of metal ions selected from titanium ions, vanadium ions, chromium ions, and zinc ions, and a concentration of the phosphorus-containing substance is 0.001 M or more and 1 M or less.

Abstract: Disclosed is a flow-type energy storage device having an improved flow of fluid. The flow-type energy storage device stores electricity using a fluidic material, and includes a reaction region in which charge-discharge reaction of electricity is performed by the fluidic material, wherein the reaction region has an octagonal cross-section. The shape of the reaction region is controlled to thus improve the flowability of the fluidic material, thereby providing a flow-type energy storage device that has almost constant electrical properties even when a charging and discharging cycle is repeatedly performed. Further, the structures of an inlet and an outlet are not complicated and a separate part for controlling the flow of fluid is not used in the device, and accordingly, additional costs are not incurred during a process of manufacturing the flow-type energy storage device.

Abstract: Disclosed herein are an electrode configured such that electrode mixture parts, each of which includes an electrode active material, and irreversible parts, each of which includes an irreversible additive, are alternately coated on one surface or both surfaces of a current collector to form an electrode pattern and a secondary battery including the same.

Abstract: Provided herein are the metalloborane compounds, MOF-metalloborane compositions, and hydrogen storage system used for high density hydrogen storage. The compounds and compositions may have the structure M2B6H6 or MOF-M2B6H6-dicarboxylic acid. Particularly the transition metal M may be titanium or scandium and the MOF may be MOF5. The hydrogen storage systems hydrogen absorbed to the metalloborane compounds or to the MOF-metalloborane compositions. Methods of storing hydrogen are provided comprising flowing or passing hydrogen gas for absorptive contact with the metalloborane compounds or to the MOF-metalloborane compositions. Also provided is a method for calculating the hydrogen storage capacity of a metalloborane is provided in which random sampling of the thermodynamic states of a two-system model of hydrogen in the presence of a metal organic framework-metalloborane crystal structure is used to calculate probability of hydrogen absorption.

Abstract: A filter module has hollow fibers which are combined into fiber bundles having end face pottings. The pottings of the fiber bundles are received into a common end disk.

Abstract: A fuel cell comprises an anode having an inner face and an outer face fluidly communicable with a fuel; a cathode having an inner face ionically communicable with and physically separated from the anode inner face, and having an outer face fluidly communicable with an oxidant; and at least one movable guard movable over at least one of the anode outer face, cathode outer face, anode inner face, and cathode inner face. The guard has a structure sufficient to block at least part of one or more of the anode's communication with the fuel, the cathode's communication with the oxidant, and the ionic communication between the anode and cathode thereby reducing a maximum potential active area of the fuel cell to an effective active area of the fuel cell.

Abstract: A gas diffusion electrode medium is for a fuel cell, has a low in-plane gas permeability and favorable water drainage characteristics in addition to high conductivity, and is able to exhibit high cell performance across a wide temperature range from low temperatures to high temperatures. The gas diffusion electrode medium is characterized by a microporous region being disposed at least at one surface of an electrode substrate, and the microporous region containing flake graphite having an aspect ratio of 50-5000.

Abstract: A non-aqueous redox flow battery includes a catholyte including a compound of formula (I), a compound of formula (II), or a compound of formula (III): wherein two R groups have the formula X, wherein X is X, wherein X is a group of formula IV-A or IV-B;

Abstract: It was an object of the invention to provide, by use of new materials and membranes and with very little outlay, an inexpensive and long-lived redox flow cell which even in the event of a possible serious accident brings about little environmental pollution by its redox-active compounds. According to the invention, high molecular weight compounds such as redox-active polymers or oligomers are provided as redox-active components and a size-exclusion membrane (3) is provided as membrane for the separation of the high molecular weight redox-active components.

Abstract: A bipolar plate and a fuel cell are provided. The bipolar plate for the fuel cell has a plurality of flow channels, and a rib is defined between neighboring two flow channels. A top surface of the rib may be a roughened surface or have a porous structure in order to improve performance of the fuel cell.

Abstract: An electrical energy store having at least one stack with in each case at least one storage cell. Each storage cell has an air electrode, which is connected to an air supply apparatus, and a storage electrode. The storage electrode adjoins channels which contain a storage medium and a steam/hydrogen mixture. A reservoir of steam/hydrogen is provided, the reservoir being directly connected to the channels.

Abstract: A porous structure including a pair of electrodes disposed in a flow direction of exhaust gas and a solid electrolyte interposed between the electrodes is arranged in an exhaust passage of an internal combustion engine, and the amount of a particulate matter in exhaust gas is specified based on a potential difference generated between the electrodes.

Abstract: An energy storage cell (20) including: an anode (40) formed of a molten alkali metal; an air cathode (60); and an electrolyte medium (50) located between the anode and cathode.

Abstract: Provided are a gas decomposition component in which an electrochemical reaction is used to reduce the running cost and high treatment performance can be achieved; and a method for producing the gas decomposition component. The gas decomposition component includes a cylindrical MEA 7 including an anode 2 on an inner-surface side, a cathode 5 on an outer-surface side, and a solid electrolyte 1 sandwiched between the anode and the cathode; a porous metal body 11s that is inserted on the inner-surface side of the cylindrical MEA and is in contact with the first electrode; and a central conductive rod 11k inserted so as to serve as an electrically conductive shaft of the porous metal body 11s.

Abstract: A fuel cell catalyst includes a platinum-iron (Pt—Fe) alloy having an ordered or disordered face-centered cubic structure or face-centered tetragonal structure. The face-centered cubic structure has a lattice constant ranging from about 3.820 ? to about 3.899 ? (or from about 3.862 ? to about 3.880 ?), and the face-centered tetragonal structure has a first lattice constant ranging from about 3.800 ? to about 3.880 ? (or from about 3.810 ? to about 3.870 ?) and a second lattice constant ranging from about 3.700 ? to about 3.810 ? (or from about 3.710 ? to about 3.800 ?). A membrane-electrode assembly can improve cell performance by including the above catalyst having the relatively high activity and selectivity for an oxidant reduction in at least one of an anode or a cathode, and can increase lifespan by inhibiting catalyst poisoning.

Abstract: A new structure-control strategy to optimize nanoparticle catalysis is provided. The presence of Au in FePtAu facilitates FePt structure transformation from chemically disordered face centered cubic (fcc) structure to chemically ordered face centered tetragonal (fct) structure, and further promotes formic acid oxidation reaction (FAOR). The fct-FePtAu nanoparticles show high CO poisoning resistance, achieve mass activity as high as about 2810 mA/mg Pt, and retain greater than 90% activity after a 13 hour stability test.

Abstract: A redox flow battery electrolyte contains 5 mg/liter or less of an organic substance having a moiety containing an aliphatic hydrocarbon containing 8 carbon atoms to 24 carbon atoms, excluding a redox flow battery electrolyte containing at least one selected from the group consisting of 1-tetradecene, n-decane, 1-octanethiol, and ester-based organic substances having a moiety containing an aliphatic hydrocarbon containing 8 carbon atoms.

Abstract: The present invention relates to a method for producing an electrochemical cell, such as in particular a secondary battery, a double-layer capacitor, an electrolytic capacitor or a fuel cell, in which a cell vessel containing two electrodes of one-piece or multi-part design and at least one separator is filled with free-flowing electrolyte. The object of the invention is to match the quantity of electrolyte in an electrochemical cell as exactly as possible to the free volume actually present. The object is achieved in that, before the filling with the electrolyte, the quantity of electrolyte to be put in is determined at least while taking into account the actual thicknesses and the actual weights of the electrodes in the cell vessel and of the separator in the cell vessel.

Abstract: The invention discloses general apparatus and methods for electrochemical energy conversion and storage via a membraneless laminar flow battery. In a preferred embodiment, the battery includes a flow-through porous anode for receiving a fuel and a porous electrolyte channel for transporting an electrolyte adjacent to the porous anode; a flow-through porous cathode is provided for transporting an oxidant; and a porous dispersion blocker is disposed between the electrolyte channel and the porous cathode, which inhibits convective mixing while allowing molecular diffusion and mean flow. Pore structure properties are selected for tuning convective dispersion, conductivity or other macroscopic properties. Specific materials, reactants, fabrication methods, and operation methods are disclosed to achieve stable charge/discharge cycles and to optimize power density and energy density.

Abstract: The present invention provides an electrolyte having high conductivity even under high-temperature low-humidification conditions (e.g. at a temperature of 100 to 120° C. and a humidity of 20 to 50% RH) and thereby makes it possible to realize a higher performance fuel cell. The present invention is a fluoropolymer electrolyte having an equivalent weight (EW) of not less than 250 but not more than 700 and a proton conductivity of not lower than 0.10 S/cm as measured at a temperature of 110° C. and a relative humidity of 50% RH and comprising a COOZ group- or SO3Z group-containing monomer unit, wherein Z represents an alkali metal, an alkaline earth metal, hydrogen atom or NR1R2R3R4 in which R1, R2, R3 and R4 each independently represents an alkyl group containing 1 to 3 carbon atoms or hydrogen atom.

Abstract: A power generation system includes an alkaline fuel cell provided with an electrolyte membrane which is an anion exchange membrane and a pair of electrodes (an anode and a cathode) arranged on the both sides of the electrolyte membrane. The alkaline fuel cell can generate an electric power by supplying a fuel gas and an oxidizing agent gas to the anode side and the cathode side, respectively. The power generation system uses a hydrogen gas containing a basic compound such as ammonia as the fuel gas to be supplied to the anode side.

Abstract: A curable composition comprising: (i) 2.5 to 50 wt % crosslinker comprising at least two acrylamide groups; (ii) 20 to 65 wt % curable ionic compound comprising an ethylenically unsaturated group and an anionic group; (iii) 15 to 45 wt % solvent; and (iv) 0 to 10 wt % of free radical initiator; wherein the molar ratio of (i):(ii) is 0.1 to 1.5. The compositions are useful for preparing ion exchange membranes.

Abstract: A curable composition comprising: (i) 2.5 to 50 wt % crosslinker comprising at least two acrylamide groups; (ii) 12 to 65 wt % curable ionic compound comprising an ethylenically unsaturated group and a cationic group; (iii) 10 to 70 wt % solvent; (iv) 0 to 10 wt % of free radical initiator; and (v) lithium and/or calcium salt. The compositions are useful for preparing ion exchange membranes.

Abstract: A curable composition comprising: (i) 2.5 to 50 wt % crosslinker comprising at least two acrylamide groups; (ii) 12 to 65 wt % curable ionic compound comprising an ethylenically unsaturated group and a cationic group; (iii) 10 to 70 wt % solvent; and (iv) 0 to 10 wt % of free radical initiator; and (v) non-curable salt; wherein the molar ratio of (i):(ii) is >0.10. The compositions are useful for preparing ion exchange membranes.

Abstract: Methods, systems and compositions that allow for treating a patient according to a patient customized therapeutic regimen are provided. Embodiments of the invention include obtaining dosage administration information from a patient and using the same to tailor a therapeutic regimen for the patient. Embodiments of the invention further include preparing and forwarding to the patient physical pharmaceutical dosages based on the customized therapeutic regimen.

Abstract: A curable composition comprising: (i) 2.5 to 50 wt % crosslinker comprising at least two acrylamide groups; (ii) 20 to 65 wt % curable ionic compound comprising an ethylenically unsaturated group and an anionic group; (iii) 15 to 45 wt % solvent; and (iv) 0 to 10 wt % of free radical initiator; wherein the composition has a pH of 0.8 to 12. The compositions are useful for preparing ion exchange membranes.

Abstract: A curable composition comprising: (i) 2.5 to 50 wt % crosslinker comprising at least two acrylamide groups; (ii) 12 to 65 wt % curable ionic compound comprising an ethylenically unsaturated group and a cationic group; (iii) 15 to 70 wt % solvent; and (iv) 0 to 10 wt % of free radical initiator; and (v) 2 to 50 wt % of non-curable salt; wherein the composition has a pH of 1 to 12. The compositions are useful for preparing ion exchange membranes.

Abstract: Power sources that enable in-body devices, such as implantable and ingestible devices, are provided. Aspects of the in-body power sources of the invention include a solid support, a first high surface area electrode and a second electrode. Embodiments of the in-power sources are configured to emit a detectable signal upon contact with a target physiological site. Also provided are methods of making and using the power sources of the invention.

Abstract: This invention provides a redox fuel cell comprising an anode and a cathode separated by an ion selective polymer electrolyte membrane; means for supplying a fuel to the anode region of the cell; means for supplying an oxidant to the cathode region of the cell; means for providing an electrical circuit between the anode and the cathode; a non-volatile catholyte solution flowing in fluid communication with the cathode, the catholyte solution comprising a redox mediator which is at least partially reduced at the cathode in operation of the cell, and at least partially regenerated by, optionally indirect, reaction with the oxidant after such reduction at the cathode, and a transition metal complex of a multidentate N-donor ligand as a redox catalyst catalyzing the regeneration of the mediator the multi-dentate N-donor ligand comprising at least one heterocyclic substituent selected from pyrrole, imidazole, 1,2,3-triazole, 1,2,4-triazole, pyrazole, pyridazine, pyrimidine, pyrazine, indole, tetrazole, quinoline, i

Abstract: Controlled activation identifiers for use in ingestible compositions, such as pharma-informatics enabled compositions, are provided. The identifiers include a controlled activation element that provides for activation of the identifier in response to the presence of a predetermined stimulus at a target site of interest. The invention finds use in a variety of different applications, including but not limited to, monitoring of therapeutic regimen compliance, tracking the history of pharmaceutical agents, etc.

Abstract: An electrochemical half-cell, comprising an active anode and/or cathode material having at least one fullerene.

Abstract: Membrane, cell and device suitable for reverse electrodialysis for the purpose of generating electricity, and methods therefor, the membrane comprising a number of channels arranged on at least a first side of the membrane, wherein the channels are suitable for throughfeed of a fluid, wherein the dimensions of the channels are aimed at obtaining a laminar flow of the fluid in the channels.

Abstract: An electrochemical cell includes a permeable fuel electrode configured to support a metal fuel thereon, and an oxidant reduction electrode spaced from the fuel electrode. An ionically conductive medium is provided for conducting ions between the fuel and oxidant reduction electrodes, to support electrochemical reactions at the fuel and oxidant reduction electrodes. A charging electrode is also included, selected from the group consisting of (a) the oxidant reduction electrode, (b) a separate charging electrode spaced from the fuel and oxidant reduction electrodes, and (c) a portion of the permeable fuel electrode. The charging electrode is configured to evolve gaseous oxygen bubbles that generate a flow of the ionically conductive medium. One or more flow diverters are also provided in the electrochemical cell, and configured to direct the flow of the ionically conductive medium at least partially through the permeable fuel electrode.

Abstract: A fuel cell stack system is configured to uniformly supply a fuel or an electrolytic solution to each of fuel cell elements, and an electronic device using the fuel cell stack system are provided. An electrolytic solution channel allowing an electrolytic solution to flow therethrough is arranged between a fuel electrode and an oxygen electrode, and a fuel channel allowing a fuel to flow therethrough is arranged outside of the fuel electrode. The electrolytic solution channels and the fuel channels of all fuel cell elements are connected in series to one another. That is, the fuel or the electrolytic solution emitted from an outlet of the fuel channel or the electrolytic solution channel of one fuel cell element enters into an inlet of the fuel channel or the electrolytic solution channel of the next fuel cell element through a connection channel.

Abstract: A flow battery includes at least one electrochemical cell that has a first electrode, a second electrode spaced apart from the first electrode and a separator arranged between the first electrode and the second electrode. A first storage portion and a second storage portion are respectively fluidly connected with the at least one electrochemical cell. A first liquid electrolyte and a second liquid electrolyte are located in the respective first storage portion and second storage portion. The first electrode has an area over which it is catalytically active with regard to the first liquid electrolyte and the second electrode has an area over which it is catalytically active with regard to the second liquid electrolyte such that the area of the first electrode is greater than the area of the second electrode.

Abstract: Ingestible event marker systems that include an ingestible event marker (i.e., an IEM) and a personal signal receiver are provided. Embodiments of the IEM include an identifier, which may or may not be present in a physiologically acceptable carrier. The identifier is characterized by being activated upon contact with a target internal physiological site of a body, such as digestive tract internal target site. The personal signal receiver is configured to be associated with a physiological location, e.g., inside of or on the body, and to receive a signal the IEM. During use, the IEM broadcasts a signal which is received by the personal signal receiver.

Abstract: A flow battery includes a liquid electrolyte having an electrochemically active specie. A flow field plate includes a first flow field channel and a second flow field channel that is separated from the first flow field channel by a rib. There is a flow path for the liquid electrolyte to flow over the rib between the channels. An electrode is arranged adjacent the flow field plate such that the liquid electrolyte that flows over the rib must flow through the electrode. The electrode includes a carbon paper that is catalytically active with regard to liquid electrolyte. The carbon paper defines a compressive strain of less than 20% at a compressive stress of 0.8 MPa and an uncompressed porosity in the range 60-85%.

Abstract: Magnesium energy storage devices that take advantage of magnesium-based anodes while maintaining practical energy densities can be useful for large-scale energy storage as well as other applications. One such device can include a negative electrode having magnesium and a positive electrode material that can flow in a batch or continuous manner. The flowable positive electrode material can result in an increased practical energy density because the fresh active material can be flowed to the positive electrode, and as a result can be theoretically infinite in size. The positive electrode can include a cathode suspension contacting a positive current collector and having particulates of a cathode magnesium intercalation compound, a cathode magnesium conversion compound, a redox active species, or combinations thereof.

Abstract: An electrolyte system for a flow battery has an anolyte including [Fe(CN)6]3? and [Fe(CN)6]4? and a catholyte including Fe2+ and Fe3+.

Abstract: Abiotic fuel cell and battery designs employing chemical dyes in alkaline solutions are disclosed. The fuel cells and batteries are capable of harnessing electrical power from various carbohydrates, including, but not limited to, glucose; in an anode design that does not require catalysts or membranes to separate half-cell reaction chambers. In certain embodiments, the abiotic fuel cell or battery designs may further employ electrodes, such as high surface area carbon materials and commercial air breathing electrodes, without the use of catalysts for glucose oxidation (i.e., precious metals or biocatalytic species). In further embodiments, organic dyes, including but not limited to, methyl viologen (MV), methylene blue, methylene green, Meldola's blue, indigo carmine, safranin O, and the like, may serve as the electron mediators. In some embodiments, the fuel cells or batteries are capable of generating power on the order of about tens of mW/cm2 from glucose and/or other types of sugars.

Abstract: A cell frame in which the structure of a positive electrode electrolyte flow path and the structure of a negative electrode electrolyte flow path are different from each other, a cell stack in which the structure of at least one of the positive electrode electrolyte flow path and the negative electrode electrolyte flow path differs between the cell frame positioned at the center and the cell frame positioned at an end, the cell stack being configured such that electrical resistance in at least one of the positive electrode electrolyte flow path and the negative electrode electrolyte flow path increases from the cell frame positioned at the center toward the cell frame positioned at the end, and a redox flow battery utilizing them.