Abstract: The present invention relates to a silicon-based composite including a silicon oxide which is coated thereon with carbon and bonded therein to lithium. The present invention also relates to a method of producing a silicon-based composite, comprising coating a surface of silicon oxide with carbon, mixing the silicon oxide coated with carbon with lithium oxide, and heat-treating a mixture of the silicon oxide coated with carbon and the lithium oxide in an inert atmosphere.

Abstract: A negative electrode for nonaqueous electrolyte secondary batteries includes a negative electrode core member and a negative electrode mixture layer attached to the negative electrode core member, wherein the negative electrode mixture layer contains negative electrode active material particles with a graphite structure and a binder, the mixture density of the negative electrode mixture layer is 1.5 g/cm3 to 1.8 g/cm3, the ratio I(002)/I(110) of the diffraction intensity I(002) of the (002) plane to the diffraction intensity I(110) of the (110) plane satisfies 60?I(002)/I(110)?120 as determined by measuring the negative electrode mixture layer by an X-ray diffraction method, the amount of particles with a size of 1 ?m to 10 ?m in the particle size distribution of a crushed product of the negative electrode mixture layer is 12% to 25% by volume.

Abstract: An anode includes a plurality of metal fibers with a three-dimensional (3D) network structure, and a silicon-containing layer having a thickness of about 0.3 ?m or less formed on a surface of and inside the 3D network structure of the plurality of metal fibers.

Abstract: An anode active material for a lithium-ion battery cell comprises low density silicon. The anode active material is provided in an anode for a lithium-ion battery. Also disclosed are methods of making the anode active material.

Abstract: The present invention relates to a method for preparing a lithium iron phosphate nanopowder, including the steps of (a) preparing a mixture solution by adding a lithium precursor, an iron precursor and a phosphorus precursor in a reaction solvent, and (b) putting the mixture solution into a reactor and heating to prepare the lithium iron phosphate nanopowder under pressure conditions of 10 to 100 bar, and a lithium iron phosphate nanopowder prepared by the method. When compared to a common hydrothermal synthesis method and a supercritical hydrothermal synthesis method, a reaction may be performed under a relatively lower pressure. When compared to a common glycothermal synthesis method, a lithium iron phosphate nanopowder having effectively controlled particle size and particle size distribution may be easily prepared.

Abstract: To simply manufacture a lithium-containing oxide at lower manufacturing cost. A method for manufacturing a lithium-containing composite oxide expressed by a general formula LiMPO4 (M is one or more of Fe (II), Mn (II), Co (II), and Ni (II)). A solution containing Li and P is formed and then is dripped in a solution containing M (M is one or more of Fe (II), Mn (II), Co (II), and Ni (II)) to form a mixed solution. By a hydrothermal method using the mixed solution, a single crystal particle of a lithium-containing composite oxide expressed by the general formula LiMPO4 (M is one or more of Fe (II), Mn (II), Co (II), and Ni (II)) is manufactured.

Abstract: An exemplary embodiment provides a lithium ion secondary battery using a high energy type anode, which enables long-life operation thereof. A secondary battery according to an exemplary embodiment comprises an electrode element in which a cathode and an anode are oppositely disposed, an electrolytic solution, and an outer packaging body which encloses the electrode element and the electrolytic solution inside; wherein the anode is formed by binding an anode active material, which comprises carbon material (a) that can absorb and desorb a lithium ion, metal (b) that can be alloyed with lithium, and metal oxide (c) that can absorb and desorb a lithium ion, to an anode collector with an anode binder; and wherein the electrolytic solution comprises a liquid medium which is hard to generate carbon dioxide at a concentration of 10 to 80 vol %.

Abstract: The present disclosure provides an anode for a secondary battery, including: an electrode current collector; a first coating layer formed on the electrode current collector and including an anode active material, a first aqueous binder and a conducting material; and a second coating layer formed on the first coating layer and including a second nonaqueous binder. Since the anode of the present disclosure can reduce volume change of the anode active material, a lithium secondary battery including same may have improved cycle characteristics.

Abstract: Disclosed herein is a cathode active material based on lithium nickel oxide represented by Formula 1, wherein the lithium nickel oxide has a nickel content of at least 40% among overall transition metals and is coated with a compound not reacting with an electrolyte (“non-reactive material”), which is selected from a group consisting of oxides, nitrides, sulfides and a mixture or combination thereof not reacting with an electrolyte, as well as a carbon material, at a surface of the lithium nickel oxide.

Abstract: A positive electrode composition for a rechargeable lithium battery includes a positive active material, a spherically shaped conductive material, and a sheet-shaped conductive material. The spherically shaped conductive material is included in an amount of about 1.1 to about 10 parts by weight based on 1 part by weight of the sheet-shaped conductive material. A positive electrode includes the positive electrode composition and a rechargeable lithium battery includes the positive electrode.

Abstract: This disclosure relates generally to cathode materials for electrochemical energy cells, more particularly to metal/air electrochemical energy cell cathode materials containing silver vanadium oxide and methods of making and using the same. The metal/air electrochemical energy cell can be a lithium/air electrochemical energy cell. Moreover the silver vanadium oxide can be a catalyst for one or more of oxidation and reduction processes of the electrochemical energy cell.

Abstract: The present invention is to provide such a carbon-supported catalyst that an activity expected from a catalytic activity by rotating disk electrode (RDE) evaluation is maintained even after the formation of a membrane electrode assembly (MEA). Disclosed is a carbon-supported catalyst wherein the carbon-supported catalyst includes fine catalyst particles that have a palladium-containing particle and a platinum-containing outermost layer covering at least part of the palladium-containing particle, and a carbon support supporting the fine catalyst particles, and wherein, in a cyclic voltammogram that is obtained by measuring, in an acid solution, the carbon-supported catalyst applied to a measurement electrode made of an electroconductive material, the proportion of the area of a hydrogen adsorption region that appears in a reduction current region to the total area of the hydrogen adsorption region and a hydrogen occlusion region that appears in the reduction current region, is 29% to 36%.

Abstract: This disclosure relates to energy storage and generation systems, e.g., combination of flow battery and hydrogen fuel cell, that exhibit operational stability in harsh environments, e.g., both charging and discharging reactions in a regenerative fuel cell in the presence of a halogen ion or a mixture of halogen ions. This disclosure also relates to energy storage and generation systems that are capable of conducting both hydrogen evolution reactions (HERs) and hydrogen oxidation reactions (HORs) in the same system. This disclosure further relates to energy storage and generation systems having low cost, fast response time, and acceptable life and performance.

Abstract: Systems for batteries or galvanic cells are disclosed. The system comprises a mixing chamber. The system further comprises a first reservoir, in fluid communication with a mixing chamber, the first reservoir configured to store a concentrated electrolyte. Additionally the system comprises a pump configured to pump a fluid into the mixing chamber. The system further comprises an electrochemical energy cell in fluid communication with the mixing chamber wherein the mixing chamber is configured to receive the fluid and concentrated electrolyte and mix the fluid and the concentrated electrolyte to produce a diluted electrolyte. Finally the system comprises the electrochemical energy cell configured to receive the diluted electrolyte, use the received diluted electrolyte for an electrochemical reaction and remove the used electrolyte solution from the cell.

Abstract: An electrical conductive member (20) includes a metal substrate (21), an intermediate layer (23) formed on the metal substrate (21), and an electrical conductive layer (25) formed on the intermediate layer (23). The intermediate layer (23) contains a constituent of the metal substrate (21), a constituent of the electrical conductive layer (25), and a crystallization inhibiting component that inhibits crystallization in the intermediate layer (23). According to this configuration, the electrical conductive member having excellent electrical conductivity and resistance to corrosion can be obtained.

Abstract: A solid oxide fuel cell having an electric power generating element unit that is configured by sandwiching a solid electrolyte layer between a fuel electrode layer and an oxygen electrode layer with a pore that is present in the solid electrolyte layer and is covered with a sealing material. In addition, a pore that is present in an interconnector, which is electrically connected to the fuel electrode layer or the oxygen electrode layer, is covered with the sealing material. Consequently, the solid oxide fuel cell is capable of easily preventing gas leakage.

Abstract: The gas distribution element for a fuel cell or an electrolyzing device including a first layer and a second layer, the first and second layers are disposed with a gas distribution structure forming a pattern for a fluid flow of a first reactant fluid. The second layer is a homogenizing element, which has first apertures, wherein at least some of the first apertures have a length and a width, with the length being greater than the width and the length extending in a transverse direction to the main direction of fluid flow.

Abstract: A gaseous fuel catalytic partial oxidation (CPOX) reformer can include a plurality or an array of spaced-apart CPOX reactor units, each reactor unit including an elongate tube having a wall with internal and external surfaces, the wall enclosing an open gaseous flow passageway with at least a portion of the wall having CPOX catalyst disposed therein and/or comprising its structure. The catalyst-containing wall structure and open gaseous flow passageway enclosed thereby define a gaseous phase CPOX reaction zone, the catalyst-containing wall section being gas-permeable to allow gaseous CPOX reaction mixture to diffuse therein and hydrogen-rich product reformate to diffuse therefrom. At least the exterior surface of a CPOX reaction zone of a CPOX reactor unit can include a hydrogen barrier. The gaseous fuel CPOX reformer also can include one or more igniters, and a source of gaseous reformable fuel.

Abstract: Integrated liquid fuel catalytic partial oxidation (CPOX) reformer and fuel cell systems can include a plurality or an array of spaced-apart CPOX reactor units, each reactor unit including an elongate tube having a gas-permeable wall with internal and external surfaces, the wall enclosing an open gaseous flow passageway with at least a portion of the wall having CPOX catalyst disposed therein and/or comprising its structure. The catalyst-containing wall structure and open gaseous flow passageway enclosed thereby define a gaseous phase CPOX reaction zone, the catalyst-containing wall section being gas-permeable to allow gaseous CPOX reaction mixture to diffuse therein and hydrogen rich product reformate to diffuse therefrom. The liquid fuel CPOX reformer also can include a vaporizer, one or more igniters, and a source of liquid reformable fuel. The hydrogen-rich reformate can be converted to electricity within a fuel cell unit integrated with the liquid fuel CPOX reactor unit.

Abstract: Integrated gaseous fuel catalytic partial oxidation (CPOX) reformer and fuel cell systems can include a plurality or an array of spaced-apart CPOX reactor units, each reactor unit including an elongate tube having a gas-permeable wall with internal and external surfaces, the wall enclosing an open gaseous flow passageway with at least a portion of the wall having CPOX catalyst disposed therein and/or comprising its structure. The catalyst-containing wall structure and open gaseous flow passageway enclosed thereby define a gaseous phase CPOX reaction zone, the catalyst-containing wall section being gas-permeable to allow gaseous CPOX reaction mixture to diffuse therein and hydrogen rich product reformate to diffuse therefrom. The gaseous fuel CPOX reformer also can include one or more igniters, and a source of gaseous reformable fuel. The hydrogen-rich reformate can be converted to electricity within a fuel cell unit integrated with the gaseous fuel CPOX reformer.

Abstract: A method for producing an electrolyte emulsion, the method including: Step (1) in which an ethylenic fluoromonomer and a fluorovinyl compound having an SO2Z1 group, wherein Z1 is a halogen element, are copolymerized at a polymerization temperature of 0° C. or higher and 40° C. or lower to provide a precursor emulsion containing a fluoropolymer electrolyte precursor; and Step (2) in which a basic reactive liquid is added to the precursor emulsion and the fluoropolymer electrolyte precursor is chemically treated, whereby an electrolyte emulsion with a fluoropolymer electrolyte dispersed therein is provided, wherein the electrolyte emulsion has an equivalent weight (EW) of 250 or more and 700 or less.

Abstract: The present invention relates to a medium and high-temperature carbon-air cell, which include a solid oxide fuel cell, a CO2 separation membrane and a carbon fuel. The solid oxide fuel cell is a tubular solid oxide fuel cell with one end closed, the carbon fuel is placed inside the tubular solid oxide fuel cell, and the CO2 separation membrane is sealed at the open end of the solid oxide fuel cell. In the carbon-air cell, with carbon as fuel and oxygen in the air as an oxidizing gas, electrochemical reactions occur. The carbon-air cell of the present invention has a novel structural design, and can achieve electricity generation with the solid oxide fuel cell without externally charging a gas, and at the same time, CO2 generated inside the solid oxide fuel cell can be discharged from the system through the CO2 separation membrane in time.

Abstract: A metal-halogen flow battery system includes a stack of flow cells, an electrolyte reservoir and one or more of a concentrated halogen return line fluidly connecting the stack to the reservoir, a venturi, a mixer, a concentrated halogen pump, or a concentrated halogen line heater.

Abstract: A system and method for aligning and reducing the relative movement between adjacent fuel cells within a fuel cell stack. The inter-cell cooperation between fuel cells along a stacking dimension is enhanced by one or more datum placed along the edge of a bipolar plate that makes up a part of a cell-containing assembly. The datum is shaped along a thickness that substantially coincides with the cell stacking dimension to avoid shifting between adjacently-stacked cells that may otherwise arise out of the occurrence of a significant acceleration along the dimension that defines the major surfaces of the plates, cells and their respective assemblies. By having the datum be integrally formed with numerous stacked cells, the need to affix individual tabs each plate is avoided.

Abstract: A method is provided for manufacturing a fuel-cell stack that has a laminate including of a plurality of fuel cells that are laminated together. In each of these fuel cells, an MEA has an anode and a cathode joined respectively to the two sides of an electrolyte membrane is sandwiched between a pair of separators. The aforementioned method has the following steps: a sealing member layout step, in which fuel cells with sealing members applied at least between adjacent fuel cells are laminated together, forming a fuel cell module; and a pressure application step, in which pressure is applied to the fuel cell module in the lamination direction of the fuel cells, forming sealed regions from the sealing members. The lamination-direction thickness of the fuel cell module is controlled by controlling the amount of pressure applied to the fuel cell module in the pressure application step.

Abstract: A device for preventing deformation of a fuel cell stack module includes vertical plates and a horizontal plate, The vertical plates and the horizontal plate are combined to form a deformation prevention frame and disposed between a plurality of fuel cell stack modules, which is vertically stacked, and on both surfaces of the respective fuel cell stack modules which are perpendicular to an end plate. Each of the plurality of fuel cell stacks includes an end plate disposed perpendicular to the vertical plates.

Abstract: There are provided an electrode assembly, and a battery cell, a battery pack, and a device. The electrode assembly includes a combination of two or more types of electrode units having different areas, wherein the electrode units are stacked such that steps are formed, and electrode units are formed such that a positive electrode and a negative electrode face one another at an interface between the electrode units.

Abstract: A method of fabricating a multilayered thin film solid state battery device. The method steps include, but are not limited to, the forming of the following layers: substrate member, a barrier material, a first electrode material, a thickness of cathode material, an electrolyte, an anode material, and a second electrode material. The formation of the barrier material can include forming a polymer material being configured to substantially block a migration of an active metal species to the substrate member, and being characterized by a barrier degrading temperature. The formation of cathode material can include forming a cathode material having an amorphous characteristic, while maintaining a temperature of about ?40 Degrees Celsius to no greater than 500 Degrees Celsius such that a spatial volume is characterized by an external border region of the cathode material. The method can then involve transferring the resulting thin film solid state battery device.

Abstract: A battery includes: an electricity-generating element that is formed by winding an electrode plate and a separator and has a space at a winding axial portion; and a spacer having an inclined portion having a width that is gradually reduced toward the center of the electricity-generating element. At least a part of the spacer is disposed in the space at the winding axial portion of the electricity-generating element, the inclined portion of the spacer abutting against an end of an inner wall of the electricity-generating element.

Abstract: A non-aqueous electrolyte secondary battery includes a positive electrode, a negative electrode, and a separator disposed between the positive electrode and the negative electrode. The positive electrode of this secondary battery contains a positive electrode active substance having a hollow structure, which has a shell portion and a hollow portion formed inside the shell portion. In addition, a heat-resistant barrier layer is disposed between the positive electrode and the separator.

Abstract: The present invention provides an electrolyte for lithium and/or lithium-ion batteries comprising a lithium salt in a liquid carrier comprising heteroaromatic compound including a five-membered or six-membered heteroaromatic ring moiety selected from the group consisting of a furan, a pyrazine, a triazine, a pyrrole, and a thiophene, the heteroaromatic ring moiety bearing least one carboxylic ester or carboxylic anhydride substituent bound to at least one carbon atom of the heteroaromatic ring. Preferred heteroaromatic ring moieties include pyridine compounds, pyrazine compounds, pyrrole compounds, furan compounds, and thiophene compounds.

Abstract: A composite electrolyte comprising includes a polymeric ionic liquid matrix; and a plurality of functionalized nanoparticles embedded therein, wherein at least one of a nitrogen cation moiety, a phosphorus cation moiety, and a sulfur cation moiety is tethered to the nanoparticle.

Abstract: A non-aqueous electrolyte including (i) a compound represented by the general formula (1): X—R—SO2F??(1) where R is a C1-12 linear or branched alkylene group optionally containing an ether bond and optionally hydrogen atoms of the alkylene group are partly substituted by a fluorine atom(s); and X is a carboxylic acid derivative group), (ii) a non-aqueous solvent and (iii) an electrolyte salt.

Abstract: A non-aqueous electrolyte secondary battery of an embodiment includes an exterior member, a negative electrode containing a titanium-containing oxide housed in the exterior member, a positive electrode housed in the exterior member, a separator housed in the exterior member and arranged between the positive electrode and the negative electrode, and a non-aqueous electrolyte solution housed in the exterior member. At least one type or more chain carbonates are contained in a solvent of the non-aqueous electrolyte solution. A self-diffusion coefficient of the chain carbonate in ?20° C. is front 1.4×10?10 to 2.0×10?10 m2/sec.

Abstract: An example electrolyte includes a solvent mixture, a lithium salt, a non-polymerizing solid electrolyte interface (SEI) precursor additive, and a solvent additive. The solvent mixture includes dimethyl carbonate (DMC) and fluoroethylene carbonate (FEC) present in a volume to volume ratio ranging from 20 to 1 to 1 to 20. The non-polymerizing SEI precursor additive is present in an amount ranging from greater than 0 wt % to about 10 wt % of a total wt % of the electrolyte, and the solvent additive is present in an amount ranging from greater than 0 wt % to about 10 wt % of the total wt % of the electrolyte.

Abstract: Elements of an electrochemical cell using an end to end process. The method includes depositing a planarization layer, which manufactures embedded conductors of said cell, allowing a deposited termination of optimized electrical performance and energy density. The present invention covers the technique of embedding the conductors and active layers in a planarized matrix of PML or other material, cutting them into discrete batteries, etching the planarization material to expose the current collectors and terminating them in a post vacuum deposition step.

Abstract: A parallel-connected electricity storage system in which a plurality of chargeable and dischargeable electricity storage elements are connected in series as an electricity storage element row and a plurality of the electricity storage element rows are connected in parallel includes an electricity-storage-element-voltage measuring device that measures an electricity storage element voltage of each of the electricity storage elements, an electricity-storage-element-state estimating device that estimates an electricity storage element state of each of the electricity storage elements, an electricity-storage-element-current measuring device that measures an electricity storage element current of each of the electricity storage element rows, a parallel-connected switch that performs connection and disconnection to and from the parallel-connected electricity storage system for each of the electricity storage element rows, and a parallel-connected-switch control means for turning on the parallel-connected switch on

Abstract: A method of charging a battery and a battery charging system, which has a relatively high charging speed while having a relatively low level of battery deterioration. The charging method includes charging a battery cell with a first current in a first constant current mode; charging the battery cell with a first voltage in a first constant voltage mode; idling the charging of the battery cell for a first idle period (t); charging the battery cell with a second current different from the first current in a second constant current mode; and charging the battery cell with a second voltage different from the first voltage in a second constant voltage mode.

Abstract: A battery pack includes a battery module, a plurality of temperature sensors, a temperature data generating unit, and a control unit. The battery module has a plurality of battery cells. The temperature data generating unit detects battery temperatures from the temperature sensors and generates battery temperature data including temperature values corresponding to the battery temperatures. The control unit determines whether or not the temperature sensors are defective based on the battery temperature data, and controls the battery module based on temperature values corresponding to temperature sensors determined not to be defective.

Abstract: An electricity storage device includes: a first battery stack (15) including a plurality of cells that are aligned in a first direction; a second battery stack (11 to 14) including a plurality of cells that are aligned in a second direction different from the first direction, the second battery stack being placed under the first battery stack; and a duct for coolant. The duct is disposed along the first battery stack and is positioned between the first battery stack and the second battery stack.

Abstract: Provided herein is a positive temperature coefficient film comprising an inorganic positive temperature coefficient compound. Also provided herein are a positive temperature coefficient electrode, a positive temperature coefficient separator, and a positive temperature coefficient lithium secondary battery, each of which comprises the positive temperature coefficient film.

Abstract: Electrochemical cells that include resistor switch assemblies that can operate according to temperature and batteries and power systems including such cells are disclosed.

Abstract: A battery pack having a cooling plate assembly and a battery module is provided. The cooling plate assembly has a pan member, first and second corrugated support members, a cover plate, and a thermally conductive layer. The pan member has first and second depressed plate portions. The first and second corrugated support members are disposed on the first and second depressed plate portions, respectively. The cover plate is coupled to the pan member such that the first and second corrugated support members are held between the cover plate and the pan member in first and second internal regions, respectively, defined by the cover plate and the pan member. The thermally conductive layer is disposed on the cover plate. The battery module is disposed on the thermally conductive layer.

Abstract: A battery pack having a battery module, a thermoelectric heat pump, and a cooling manifold is provided. The battery module has a first battery cell, a housing, and a first solid cooling fin. A first panel portion of the first solid cooling fin is disposed against the first battery cell. A second panel portion of the first solid cooling fin is disposed on an outer surface of the housing and is coupled to an end portion of the first panel portion. A first side of the thermoelectric heat pump is disposed against the second panel portion, and a second side of the thermoelectric heat pump is disposed against the cooling manifold. The thermoelectric heat pump transfers heat energy from the first solid cooling fin to the cooling manifold in response to a first electrical current flowing through the thermoelectric heat pump in a first direction, to reduce a temperature level of the first battery cell.

Abstract: This invention provides a shutdown system and methods for battery shutdown followed by a standby mode using a washing solution controlled by pH such that the electrode remains stable.

Abstract: A lithium-air electrochemical cell is provided. The battery comprises: an anode compartment; a cathode compartment; and a lithium ion conductive membrane separating the anode compartment from the cathode compartment. The anode compartment comprises an anode having lithium or a lithium alloy as active metal and a lithium ion electrolyte, while the cathode compartment comprises an air electrode and an ionic liquid capable of supporting the reduction of oxygen. A lithium ion concentration in the cathode compartment is such that the lithium ion concentration is greatest at the lithium ion selective membrane and lowest at the cathode.

Abstract: A rechargeable electrochemical battery cell includes a molten carbonate salt electrolyte whose anion transports oxygen between a metal electrode and an air electrode on opposite sides of the electrolyte, where the molten salt electrolyte is retained inside voids of a porous electrolyte supporting structure sandwiched by the electrodes, and the molten salt includes carbonate including at least one of the alkaline carbonate including Li2Co2, NA2CO2, and K2CO2, having a melting point between 400° C. and 800° C.

Abstract: A reliable, end-to-end power supply solution for components of a telecommunications network provides either a primary source or a backup source of electrical power at various telecommunications sites for reliable operation of telecommunications equipment. One subsystem of the power supply solution includes one or more proton exchange membrane type fuel cells and an energy storage device for storing DC electrical power produced by the fuel cells. Another subsystem includes one or more microturbine generators, one or more rectifiers for converting AC electrical power produced by the microturbine generators to DC electrical power, and one or more proton exchange membrane type fuel cells for producing DC electrical power. The power supply solution ensures that voice and data traffic is reliably handled by a telecommunications network in situations where commercial electric utilities fail to supply power at certain points along the network.

Abstract: A non-magnetic material frequency selective limiter circuit has first and second resonators and a non-linear coupling component. The first resonator oscillates at a fundamental frequency. The second resonator oscillates at one half of the fundamental frequency. The non-linear coupling component non-linearly and parametrically couples the first resonator and the second resonator. The first resonator, second resonator and the non-linear coupling component are arranged so as to reduce the amplitude of an output signal for an input signal of frequency ? when an input signal amplitude is above a voltage threshold value, by converting part of the input signal to a signal at the frequency ?/2. The first resonator, second resonator and the non-linear coupling component are formed of non-magnetic materials.

Abstract: A resonance device and a filter including the same are provided. The resonance device includes a case having a first ground surface and a second ground surface which are facing each other, and a first conductive layer located in the case, and the first conductive layer includes a main part grounded via the first ground surface, and a protruding part which has a width different from that of the main part and is located to be spaced apart from the second ground surface.