Abstract: A negative electrode material for a lithium-ion secondary battery containing a composite (C) that contains a porous carbon (A) and a Si-containing compound (B). The porous carbon (A) satisfies V1/V0>0.80 and V2/V0<0.10. When a total pore volume at the maximum value of a relative pressure P/P0 is defined as V0 and P0 is a saturated vapor pressure, a cumulative pore volume at a relative pressure P/P0=0.1 is defined as V1, and a cumulative pore volume at a relative pressure P/P0=10?7 is defined as V2 in a nitrogen adsorption test. Further, the porous carbon (A) has a BET specific surface area of 800 m2/g or more, and the Si-containing compound (B) is contained in pores of the porous carbon (A). Also disclosed is a negative electrode sheet including the negative electrode material and a lithium-ion secondary battery including the negative electrode sheet.

Abstract: A solid ion conductive layer can include a foamed matrix and an electrolyte material including a hygroscopic material. In an embodiment, the electrolyte material can include a halide-based material, a sulfide-based material, or any combination thereof. In another embodiment, the solid ion conductive layer can include total porosity of at least 30 vol % for a total volume of the solid ion conductive layer.

Abstract: A battery includes a stacked arrangement of electrochemical cells. Each electrochemical cell is free of a cell housing and includes a bipolar plate having a substrate, a first active material layer formed on a first surface of the substrate, and a second active material layer formed on a second surface of the substrate. Each cell includes a solid electrolyte layer that encapsulates at least one of the active material layers, and an edge insulating device that is disposed between the peripheral edges of the substrates of each pair of adjacent cells. A support frame surrounds the cell stack and is configured to receive and support the outer peripheral edge of the edge insulating device of each cell.

Abstract: In one embodiment of the present disclosure, a composition for producing a vanadium electrolyte includes a vanadium compound and an ion solution containing vanadium ions and hydrogen ions. In another embodiment, a method for producing a vanadium electrolyte includes obtaining a vanadium compound, and mixing the vanadium compound with an ion solution containing vanadium ions and hydrogen ions.

Abstract: The power storage device includes power storage units arranged with a conductive plate interposed therebetween in the vertical direction, each of the power storage units includes an electrode stack including bipolar electrodes stacked with a separator interposed therebetween, and a sealing member provided around the electrode stack so as to seal a housing space formed between adjacent electrodes of the electrode stack. At least one of the power storage units is provided with an overhang member on an outer peripheral surface of the sealing member. The overhang member includes an inclined portion that extends from the outer peripheral surface of the sealing member toward the outside of the power storage unit and inclines downward as it leaves away from the outer peripheral surface of the sealing member, and a top portion formed at a lower end of the inclined portion.

Abstract: New or improved lead acid batteries with vapor pressure barriers and/or improved battery separators, as well as systems, vehicles, and/or methods of manufacture and/or use thereof are disclosed herein. In at least select embodiments, the instant disclosure provides new or improved lead acid batteries with a vapor pressure barrier. In at least select embodiments, the instant disclosure provides new or improved lead acid battery vapor pressure barriers along with new or improved battery separators, and/or methods of manufacture and/or use thereof. In at least select embodiments, the instant disclosure provides a new or improved lead acid battery with a vapor pressure barrier that reduces the water loss from the battery. In at least select embodiments, a method of reducing the water loss of a lead acid battery may include providing a vapor pressure barrier, such as a layer of oil, inside the lead acid battery along with an improved battery separator.

Abstract: Stable and high performance positive and negative electrolytes compositions to be used in redox flow battery systems are described. The redox flow battery system, comprises: at least one rechargeable cell comprising a positive electrolyte, a negative electrolyte, and an ionically conductive membrane positioned between the positive electrolyte and the negative electrolyte, the positive electrolyte in contact with a positive electrode, and the negative electrolyte in contact with a negative electrode. The positive electrolyte consists essentially of water, a first amino acid, an inorganic acid, an iron precursor, a supporting electrolyte, and optionally a boric acid. The negative electrolyte consists essentially of water, the iron precursor, the supporting electrolyte, and a negative electrolyte additive. The iron precursor is FeCl2, FeCl3, FeSO4, Fe2(SO4)3, FeO, Fe, Fe2O3, or combinations thereof. The supporting electrolyte is LiCl, NaCl, Na2SO4, KCl, NH4Cl, or combinations thereof.

Abstract: Disclosed are electrode plates for a lead acid battery. The electrode plates are formed of an electrode plate having a face, the electrode plate comprising a lead or lead alloy grid coated with an active material and the electrode plates having a porous, non-woven mat comprised of polymer fibers coating on the face of the electrode plate, as well as a method for making the coated electrode plates and lead acid batteries containing the coated electrode plates.

Abstract: A lithium-sulfur battery comprising a separator in which an adsorption layer including a radical compound having a nitroxyl radical site is formed, and in particular, to a lithium-sulfur battery suppressing elution of lithium polysulfide by using an adsorption layer including a radical compound having a nitroxyl radical site and optionally a conductive material on at least one surface of a separator. In the lithium-sulfur battery, elution and diffusion may be prevented by a radical compound having a nitroxyl radical site, a stable radical compound, adsorbing lithium polysulfide eluted from positive electrode, and in addition thereto, electrical conductivity is further provided to provide a reaction site of a positive electrode active material, and as a result, battery capacity and lifetime properties are enhanced.

Abstract: The battery pack according to the present disclosure includes a cell module assembly, a pack case including a case body to receive the cell module assembly and a case cover coupled with the case body to package the cell module assembly, and a horizontal protruding rib protruding toward the cell module assembly in a direction parallel to a stack direction of cells in the cell module assembly at an inner lower end of the case body, wherein the horizontal protruding rib is a double rib structure including a first rib which is compressed by the cell module assembly to absorb a thickness tolerance of the cell module assembly, and an uncompressible second rib which is provided on an outer side of the first rib and disposed at a more rear position than the first rib to reinforce the first rib.

Abstract: Battery components are generally provided. In some embodiments, the battery components can be used as pasting paper and/or capacitance layers for batteries, such as lead acid batteries. The battery components described herein may comprise a plurality of fibers. The battery component may include, in some embodiments, a plurality of fibers and, optionally, one or more additives such as conductive carbon and/or activated carbon. In certain embodiments, the plurality of fibers include relatively coarse glass fibers (e.g., having an average diameter of greater than or equal to 2 microns), relatively fine glass fibers (e.g., having an average diameter of less than 2 microns), and/or fibrillated fibers. In some instances, such fibers may be present in amounts such that the battery component has a particular surface area, mean pore size, and/or dry tensile strength.

Abstract: A machine-implemented social networking system builds up and repeatedly refreshes a hierarchy tree containing topic nodes. New nodes are added as new topics emerge in online public forums. Each topic node can link to an on-topic real time chat room whose occupants are currently discussing the topic of the node. A chat room can be pointed to by more than one node if the room is discussing multiple topics. Rooms can migrate from node to node as room topic dynamically changes. A system user who explicitly or inferentially wishes to be invited into a chat room which is on-topic with what the user is currently focused upon can do so by use of a node-seeking automated process. The process operates in the background and seeks out nodes of the hierarchy tree that currently have topics appearing to be the same as or similar to what topics the user appears to have in mind.

Abstract: Disclosed are electrode plates for a lead acid battery. The electrode plates are formed of an electrode plate having a face, the electrode plate comprising a lead or lead alloy grid coated with an active material and the electrode plates having a porous, non-woven mat comprised of polymer fibers coating on the face of the electrode plate, as well as a method for making the coated electrode plates and lead acid batteries containing the coated electrode plates.

Abstract: A carbon material having a continuous porous structure oriented to the stretching axis is provided, which carbon material can be used as a structural material excellent in interfacial adhesion. The porous carbon material has a continuous porous structure in at least a portion thereof, in which the continuous porous structure has an orientation degree measured by a small-angle X-ray scattering method or an X-ray CT method of 1.10 or more.

Abstract: Disclosed herein are soluble content absorbent glass mats or AGM separators for VRLA, AGM, or VRLA AGM batteries. Such glass mats may be prepared from insoluble glass fibers blended with soluble content materials. Upon exposure to a suitable solvent, the dissolving or solvating of the soluble content produces voids within the glass mat. The voids enhance the absorption of the solvent within the glass mat. The soluble content may be acid-soluble glass fibers or microfibers.

Abstract: Disclosed herein are compositions, which can be used to coat electrode plates, comprising at least one carbonaceous material and at least one additive, wherein the at least one additive comprises a metal ion selected from calcium, barium, potassium, magnesium, and strontium ion, and wherein the metal ion is present in an amount ranging from 0.5 wt. % to 3 wt. % relative to the total weight of carbonaceous material. Also disclosed are electrodes and lead acid batteries comprising such compositions, and methods of making the compositions.

Abstract: A vehicle battery packaging for accommodating a plurality of longitudinal battery cells, wherein the battery cells are arranged in a frame in parallel with respect to their longitudinal axes, and wherein each battery cell has a first end and an opposite second end with respect to the longitudinal axis, the battery packaging including: a conductor plate adapted to electrically couple to the second ends of the battery cells; a cooling plate thermally coupled to the conductor plate; and a gap filler layer sandwiched between the conductor plate and the cooling plate.

Abstract: An electric storage device is provided with an electrode assembly including a positive electrode plate and a negative electrode plate; a case for housing the electrode assembly; a positive-electrode external terminal arranged on an outer surface of the case and electrically connected to the positive electrode plate; a negative-electrode external terminal arranged on an outer surface of the case and electrically connected to the negative electrode plate; and a gas exhaust valve formed in a region of the case on the opposite side of a region where the positive-electrode external terminal and the negative-electrode external terminal are arranged.

Abstract: A metal alloy for use in a wire included in an electrochemical cell is disclosed having an amorphous structure, microcrystalline grains, or grains that are sized less than about one micron. In various embodiments, the microcrystalline grains are not generally longitudinally oriented, are variably oriented, or are randomly oriented. In some embodiments, the microcrystalline grains lack uniform grain size or are variably sized. In some embodiments, the microcrystalline grains have an average grain size of less than or equal to 5 microns. In some embodiments, the metal alloy lacks long-range crystalline order among the microcrystalline grains. In some embodiments, the wire is used in a substrate used in the electrochemical cell. In some embodiments, the metal alloy is formed using a co-extrusion process comprising warming up the metallic alloy and applying pressure and simultaneously passing a core material through a die to obtain a composite structure.

Abstract: A valve regulated lead-acid battery includes a positive electrode plate, a retainer mat and a negative electrode plate housed in a container and holding an electrolyte solution respectively. The electrolyte solution contains colloidal silica and lithium ions.

Abstract: A nonaqueous electrolyte battery includes a negative electrode including a current collector and a negative electrode active material having a Li ion insertion potential not lower than 0.4V (vs. Li/Li+). The negative electrode has a porous structure. A pore diameter distribution of the negative electrode as determined by a mercury porosimetry, which includes a first peak having a mode diameter of 0.01 to 0.2 ?m, and a second peak having a mode diameter of 0.003 to 0.02 ?m. A volume of pores having a diameter of 0.01 to 0.2 ?m as determined by the mercury porosimetry is 0.05 to 0.5 mL per gram of the negative electrode excluding the weight of the current collector. A volume of pores having a diameter of 0.003 to 0.02 ?m as determined by the mercury porosimetry is 0.0001 to 0.02 mL per gram of the negative electrode excluding the weight of the current collector.

Abstract: A system for energy generation or storage on an electrochemical basis includes at least one flow cell, each flow cell including two half-cells through which differently charged electrolyte liquids (21, 22) flow and which are separated by a membrane, at least one electrode being disposed in each of these half-cells, and a tank for each of the electrolyte liquids. A common gas volume (23) connecting the tanks is provided, and at least one catalyst (24) for reducing a positive reaction partner of then redox pair in contact with the positive electrolyte liquid (22) and also with the common gas volume (23) is disposed in the tank for the positive electrolyte liquid (22).

Abstract: An electrochemical cell provided with two half cells. A pressure or density differential is created between the cathode and anode electrodes, each of which is contained in one of the half cells. The pressure or density differential is created by single or multiple sources including compression, vacuum, weight (gravity) of mass, chemical, molecular, or, pressure or density differentials created by thermal gradients.

Abstract: A lead-acid battery activator characterized in that alkali polyacrylate solid particles are dispersed in the sulfuric acid aqueous solution, which is intended to extend the battery life by preventing the sulfation of negative electrode, and a lead-acid battery using said activator.

Abstract: An Advanced Graphite, with a lower degree of ordered carbon domains and a surface area greater than ten times that of typical battery grade graphites, is used in negative active material (NAM) of valve-regulated lead-acid (VRLA) type Spiral wound 6V/25 Ah lead-acid batteries. A significant and unexpected cycle life was achieved for the Advanced Graphite mix, where the battery was able to cycle beyond 145,000 cycles above the failure voltage of 9V, in a non-stop, power-assist, cycle-life test. Batteries with Advanced Graphite also showed increased charge acceptance power and discharge power compared to control groups.

Abstract: The present disclosure provides an embodiment of an integrated structure that includes a first electrode of a first conductive material embedded in a first semiconductor substrate; a second electrode of a second conductive material embedded in a second semiconductor substrate; and a electrolyte disposed between the first and second electrodes. The first and second semiconductor substrates are bonded together through bonding pads such that the first and second electrodes are enclosed between the first and second semiconductor substrates. The second conductive material is different from the first conductive material.

Abstract: There is disclosed a lead storage battery comprising a group of plates housed in a battery jar, and an electrolyte injected therein to impregnate the group of plates with the electrolyte, thus performing formation treatment, the lead storage battery being adapted to be used in a partial state of charge where the state of charge is confined within the range of more than 70% to less than 100%, wherein the group of plates are formed of a stack constituted by a large number of negative substrates comprising grid substrates filled with a negative active material, by a large number of positive substrates comprising grid substrates filled with a positive active material, and by a porous separator interposed between the negative electrodes and positive electrodes, and the electrolyte contains at least one kind of ion selected from the group consisting of aluminum ions, selenium ions and titanium ions.

Abstract: A redox flow battery having a supporting solution that includes Cl? anions is characterized by an anolyte having V2+ and V3+ in the supporting solution, a catholyte having Fe2+ and Fe3+ in the supporting solution, and a membrane separating the anolyte and the catholyte. The anolyte and catholyte can have V cations and Fe cations, respectively, or the anolyte and catholyte can each contain both V and Fe cations in a mixture. Furthermore, the supporting solution can contain a mixture of SO42? and Cl? anions.

Abstract: A load variation detecting section determines whether or not the actual load variation falls below a load variation threshold stored in a memory. If a load variation detecting section determines that a specific time period (for example, one minute) has elapsed since the actual load variation fell below a load variation threshold, a power supply section applies same power to reactors for the respective phases. On the other hand, a heat dissipation property calculating section measures temperature-rise rates of the elements for the respective phases, ranks the rates in order from the one having a higher heat dissipation property, and notifies the priority drive phase determining section of the result. A priority drive phase determining section chooses a phase having the highest heat dissipation property as a priority drive phase.

Abstract: A flooded lead-acid battery includes a negative active material, a positive active material having lead dioxide as a main component, and an electrolyte solution that contains sulfuric acid and is flowable. The negative active material of the flooded lead-acid battery contains carbon, a water-soluble polymer formed of a bisphenol condensation product having a sulfonic acid group, and a cellulose ether. The flooded lead-acid battery has low turbidity of the electrolyte solution and is excellent in high rate discharge performance at low temperature, regenerative charge accepting performance, and endurance performance in a partially charged state.

Abstract: Provided is a battery which can prevent deactivation from occurring by avoiding solid deposition at electrodes. The battery includes an anion conductor, a positive electrode, a negative electrode, a first aqueous liquid electrolyte layer and a second aqueous liquid electrolyte layer, wherein the first aqueous liquid electrolyte layer and the positive electrode are present in this sequence on a first surface of the anion conductor, and the second aqueous liquid electrolyte layer and the negative electrode are present in this sequence on a second surface of the anion conductor, and wherein the negative electrode includes a negative electrode active material layer, and the negative electrode active material layer includes a negative electrode active material which can release a metal ion upon discharging.

Abstract: Herein provided is an electrochemical cell electrolyte formed from ingredients comprising: water, sulfuric acid, and at least one octylphenol ethoxylate of Formula 1: where n is a natural number from at least 1 to at most 16.

Abstract: Representative embodiments provide a liquid or gel separator utilized to separate and space apart first and second conductors or electrodes of an energy storage device, such as a battery or a supercapacitor. A representative liquid or gel separator comprises a plurality of particles, typically having a size (in any dimension) between about 0.5 to about 50 microns; a first, ionic liquid electrolyte; and a polymer. In another representative embodiment, the plurality of particles comprise diatoms, diatomaceous frustules, and/or diatomaceous fragments or remains. Another representative embodiment further comprises a second electrolyte different from the first electrolyte; the plurality of particles are comprised of silicate glass; the first and second electrolytes comprise zinc tetrafluoroborate salt in 1-ethyl-3-methylimidalzolium tetrafluoroborate ionic liquid; and the polymer comprises polyvinyl alcohol (“PVA”) or polyvinylidene fluoride (“PVFD”).

Abstract: An electrode plate for a battery comprising a plurality of electrodes in a grid where the grid defines a plurality of spaces. A paste disposed in the spaces has a top surface and a bottom surface. The paste is narrowed in the space, defining a distance between the top surface of the paste and the bottom surface of the paste that is less than the thickness of the plate over the electrodes. A retention layer of porous fabric is impressed on the top and/or bottom surface of the paste. Electrolyte disposed in electric communication with the electrodes.

Abstract: Provided is a battery which can prevent deactivation from occurring by avoiding solid deposition at electrodes. The battery includes an anion conductor, a positive electrode, a negative electrode, a first aqueous liquid electrolyte layer and a second aqueous liquid electrolyte layer, wherein the first aqueous liquid electrolyte layer and the positive electrode are present in this sequence on a first surface of the anion conductor, and the second aqueous liquid electrolyte layer and the negative electrode are present in this sequence on a second surface of the anion conductor, and wherein the negative electrode includes a negative electrode active material layer, and the negative electrode active material layer includes a negative electrode active material which can release a metal ion upon discharging.

Abstract: The present application is directed to methods for preparation of carbon materials. The carbon materials comprise enhanced electrochemical properties and find utility in any number of electrical devices, for example, as electrode material in ultracapacitors or batteries.

Abstract: A method for cleaning a semiconductor structure includes subjecting a semiconductor structure to an aqueous solution including at least one fluorine compound, and at least one strong acid, the aqueous solution having a pH of less than 1. In one embodiment, the aqueous solution includes water, hydrochloric acid, and hydrofluoric acid at a volumetric ratio of water to hydrochloric acid to hydrofluoric acid of 1000:32.5:1. The aqueous solution may be used to form a contact plug that has better contact resistance and improved critical dimension bias than conventional cleaning solutions.

Abstract: An electrode for a lead-acid voltaic cell comprises a high surface area, high porosity 3-dimensional lattice structure wherein the core elements forming the lattice are substantially contiguous. The core elements are coated with one or more corrosion resistant and conductive materials, and solid active materials are coated on the core elements and retained within the matrix. The lattice structure acts as the current collector.

Abstract: An energy storage device including an active electrolyte, a first electrode and a second electrode is provided. The active electrolyte contains protons and ion pairs with a redox ability. The first electrode and the second electrode coexist in the active electrolyte and are separated from each other. The first electrode and the second electrode respectively include an active material producing a redox-reaction with the active electrolyte or an active material producing ion adsorption/desorption with the active electrolyte. The active electrolyte receives electrons from the first electrode and/or the second electrode so as to perform a redox-reaction for charge storage.

Abstract: A secondary battery includes: a cathode; an anode; and an electrolytic solution. The electrolytic solution includes a cyano cyclic ester carbonate represented by Formula (1) described below and one or more of compounds represented by Formula (2) to Formula (6) described below.

Abstract: The disclosure describes compositions and methods for producing a change in the voltage at which hydrogen gas is produced in a lead acid battery. The compositions and methods relate to producing a concentration of one or more metal ions in the lead acid battery electrolyte.

Abstract: The disclosure describes compositions and methods for producing a change in the voltage at which hydrogen gas is produced in a lead acid battery. The compositions and methods relate to producing a concentration of one or more metal ions in the lead acid battery electrolyte.

Abstract: The disclosure describes compositions and methods for producing a change in the voltage at which hydrogen gas is produced in a lead acid battery. The compositions and methods relate to producing a concentration of one or more metal ions in the lead acid battery electrolyte.

Abstract: A plastics electrode material includes a mixture having a nitrogen-containing conductive polymer and a conductive carbon material mixed with the polymer. The polymer is polyquinoline, polyphenylquinoxaline, polycarbazole, polypyridine, polypyrrole, polyaniline or polyindole. The conductive carbon material is 1% to 40% by weight of the mixture. The mixture is activated by a 0.2 M to 5 M proton-containing acidic electrolytic solution. The present invention further comprises second cells using the plastics electrode material. Because the conductive carbon material and high concentration acidic electrolytic solution are added to the polymer, the plastics electrode material has a high conductivity. Thus, the secondary cells have a high efficiency of charging and discharging and a long cyclic life.

Abstract: A lead-acid battery or cell comprises electrode(s) of with current collector(s) of a fibrous material with an average interfibre spacing of less than 50 microns. The current collector material may be a carbon fibre material which has been thermally treated by electric arc discharge. The fibrous current collector material may comprise an impregnated paste comprising a mixture of lead sulphate particles and dilute sulfuric acid.

Abstract: The present application is directed to blends comprising a plurality of carbon particles and a plurality of lead particles. The blends find utility in any number of electrical devices, for example, in lead acid batteries. Methods for making and using the blends are also disclosed.

Abstract: The present invention is directed to energy storage devices, such as lead-acid batteries, and methods of improving the performance thereof, through the incorporation of one or more carbon-based additives.

Abstract: A secondary battery capable of suppressing resistance rise even after repeated charge and discharge is provided. The secondary battery includes a cathode, an anode, and an electrolytic solution. The anode contains titanium-containing lithium composite as an anode active material, and the electrolytic solution contains cyclic disulfonic acid anhydride.

Abstract: A lead-acid battery comprising: at least one lead-based negative electrode; at least one lead dioxide-based positive electrode; at least one capacitor electrode; and electrolyte in contact with the electrodes; wherein a battery part is formed by the lead based negative electrode and the lead dioxide-based positive electrode; and an asymmetric capacitor part is formed by the capacitor electrode and one electrode selected from the lead based negative electrode and the lead-dioxide based positive electrode; and wherein all negative electrodes are connected to a negative busbar, and all positive electrodes are connected to a positive busbar. The capacitor electrode may be a capacitor negative electrode comprising carbon and an additive mixture selected from oxides, hydroxides or sulfates of lead, zinc, cadmium, silver and bismuth, or a capacitor negative electrode comprising carbon, red lead, antimony in oxide, hydroxide or sulfate form, and optionally other additives.

Abstract: To provide a method for producing a lead-acid battery negative plate for use in a storage battery which provides improved deteriorated rapid discharge characteristics by preventing an interfacial separation between a negative active material-filled plate and a carbon mixture-coated layer, which is a problem in a negative plate having such a configuration that the carbon mixture coated layer is formed on the surface of the negative active material-filled plate. A coating layer of a carbon mixture is formed at least in a part of a surface of a negative active material-filled plate. The carbon mixture is prepared by mixing two kinds of carbon materials consisting of a first carbon material having conductive properties and a second carbon material having capacitive capacitance and/or pseudo capacitive capacitance and a binding agent. Subsequently, a sufficient amount of lead ions are generated enough to be moved from the negative active Material-filled plate into the carbon mixture-coated layer.