Abstract: The current disclosure relates to an anode material with the general formula MySb-M?Ox—C, where M and M? are metals and M?Ox—C forms a matrix containing MySb. It also relates to an anode material with the general formula MySn-M?Cx—C, where M and M? are metals and M?Cx—C forms a matrix containing MySn. It further relates to an anode material with the general formula Mo3Sb7—C, where —C forms a matrix containing Mo3Sb7. The disclosure also relates to an anode material with the general formula MySb-M?Cx—C, where M and M? are metals and M?Cx—C forms a matrix containing MySb. Other embodiments of this disclosure relate to anodes or rechargeable batteries containing these materials as well as methods of making these materials using ball-milling techniques and furnace heating.

Abstract: A composite cathode active material, a method of preparing the composite cathode active material, a cathode including the composite cathode active material, and a lithium battery including the cathode. The composite cathode active material includes a lithium intercalatable material; and a garnet oxide, wherein an amount of the garnet oxide is about 1.9 wt % or less, based on a total weight of the composite cathode active material.

Abstract: Disclosed are precursor particles of a lithium composite transition metal oxide for lithium secondary batteries, wherein the precursor particles of a lithium composite transition metal oxide are composite transition metal hydroxide particles including at least two transition metals and having an average diameter of 1 ?m to 8 ?m, wherein the composite transition metal hydroxide particles exhibit monodisperse particle size distribution and have a coefficient of variation of 0.2 to 0.7, and a cathode active material including the same.

Abstract: Embodiments of the present disclosure provide for materials that include conch shell structures, methods of making conch shell slices, devices for storing energy, and the like.

Abstract: Provided is a lithium mixed transition metal oxide having a composition represented by Formula I of LixMyO2 (M, x and y are as defined in the specification) having mixed transition metal oxide layers (“MO layers”) comprising Ni ions and lithium ions, wherein lithium ions intercalate into and deintercalate from the MO layers and a portion of MO layer-derived Ni ions are inserted into intercalation/deintercalation layers of lithium ions (“reversible lithium layers”) thereby resulting in the interconnection between the MO layers. The lithium mixed transition metal oxide of the present invention has a stable layered structure and therefore exhibits improved stability of the crystal structure upon charge/discharge. In addition, a battery comprising such a cathode active material can exhibit a high capacity and a high cycle stability.

Abstract: The present invention generally relates to methods and systems for carrying out a pH-influenced chemical and/or biological reaction. In some embodiments, the pH-influenced reaction involves the conversion of CO2 to a dissolved species.

Abstract: The present invention provides a LiCoO2-containing powder comprising LiCoO2 having a stoichiometric composition via heat treatment of a lithium cobalt oxide and a lithium buffer material to make equilibrium of a lithium chemical potential therebetween; a lithium buffer material which acts as a Li acceptor or a Li donor to remove or supplement Li-excess or Li-deficiency, coexisting with a stoichiometric lithium metal oxide; and a method for preparing a LiCoO2-containing powder. Further, provided is an electrode comprising the above-mentioned LiCoO2-containing powder as an active material, and a rechargeable battery comprising the same electrode.

Abstract: A composition comprising a Type 1 clathrate of silicon having a Si46 framework cage structure wherein the silicon atoms on said framework are at least partially substituted by carbon atoms, said composition represented by the formula CySi46-y with 1?y?45. The composition of may include one or more guest atoms A within the cage structure represented by the formula AxCySi46-y wherein A=H, Li, Na, K, Rb, Cs, Fr, Be, Mg, Ca. Sr, Ba, Ra, Eu, Cl, Br, or I or any metal or metalloid element and x is the number of said guest atoms within said cage structure.

Abstract: To provide an active material with high capacity, high initial charge-discharge efficiency, and high average discharge voltage. An active material according to the present invention includes a first active material and a second active material, wherein the ratio (?) of the second active material (B) to the total amount by mole of the first active material (A) and the second active material (B) satisfies 0.4 mol %???18 mol % [where ?=(B/(A+B))×100].

Abstract: A solid ion conductor including a garnet oxide represented by Formula 1: L5+x+2y(Dy,E3-y)(Mez,M2-z)Od??Formula 1 wherein L is at least one of a monovalent cation or a divalent cation, D is a monovalent cation, E is a trivalent cation, Me and M are each independently a trivalent, tetravalent, pentavalent, or a hexavalent cation, 0<x+2y?3, 0?y?0.5, 0?z<2, and 0<d?12, wherein O is partially or totally substituted with at least one of a pentavalent anion, a hexavalent anion, or a heptavalent anion; and B2O3.

Abstract: The present invention relates to a lithium secondary battery including a cathode, an anode, a separator disposed between the cathode and the anode, and a non-aqueous electrolyte. An ionomer is included in at least one element selected from the group consisting of the cathode, the anode, the separator, and the non-aqueous electrolyte.

Abstract: A method of creating an electrolyte film includes mixing succinonitrile (SCN), lithium salt and crosslinkable polyether addition to form an isotropic amorphous mixture; and crosslinking the crosslinkable polyether to form a cured film, wherein the cured film remains amorphous without undergoing polymerization-induced phase separation or crystallization.

Abstract: Material compositions are provided that may comprise, for example, a vertically aligned carbon nanotube (VACNT) array, a conductive layer, and a carbon interlayer coupling the VACNT array to the conductive layer. Methods of manufacturing are provided. Such methods may comprise, for example, providing a VACNT array, providing a conductive layer, and bonding the VACNT array to the conductive layer via a carbon interlayer.

Abstract: A particulate precursor compound for manufacturing an aluminum doped lithium transition metal (M)-oxide powder usable as an active positive electrode material in lithium-ion batteries includes a transition metal (M)-hydroxide or (M)-oxyhydroxide core and a non-amorphous aluminum oxide coating layer covering the core. By providing an aluminum dry-coating process where the particulate precursor core compound is mixed with alumina powder in one or more procedures, higher doping levels of aluminum compared to the known prior art may be achieved. The crystal structure of the alumina is maintained during the coating procedures and the core of each mixed transition metal precursor particle is surrounded by a coating layer containing crystalline alumina nano particles. The aluminum concentration in the particulate precursor decreases as the size of the core increases.

Abstract: Disclosed is a positive electrode active substance for a non-aqueous electrolyte secondary battery including a composite oxide containing lithium and nickel, in which the positive electrode active substance has a structure of secondary particles formed by aggregation of primary particles. The average particle diameter of the primary particles (D1) is 0.9 ?m or less. The average particle diameter of the primary particles (D1) and the standard deviation (?) of the average particle diameter of the primary particles (D1) meet the relationship of D1/?2?24.

Abstract: The present invention relates to a lithium battery positive electrode comprising an active substance that can occlude and release lithium ion, a carbon-based conductivity enhancer, and a binder, characterized in that the positive electrode contains the carbon-based conductivity enhancer in an amount of 0.1 to 2 mass % on the basis of the entire mass of the positive electrode, and that the carbon-based conductivity enhancer contains a carbon fiber having a mean fiber diameter of 1 to 200 nm, wherein the active substance that can occlude and release lithium ion is contained in an amount, as calculated from the true density of the active substance, of 70% by volume or more on the basis of the total volume of the positive electrode; and relates to a lithium battery using the a lithium battery positive electrode. The positive electrode obtained by the present invention has an excellent electrolyte permeability and electrolyte retention. Therefore, it is better adapted to high-density lithium battery.

Abstract: A positive electrode material for a lithium-ion cell, comprising an over-lithiated layered lithium metal composite oxide that provides the positive electrode material for a lithium-ion cell. Also, a method for manufacturing an over-lithiated layered lithium metal composite oxide represented by the general formula Li1+xM1?xO2, where x is 0.10 or more and 0.33 or less, and M includes Mn and at least one element selected from the group consisting of Ni, Co, Al, Mg, Ti, Fe and Nb, wherein the method includes a step of mixing a lithium metal composite oxide represented by the general formula Li1+xM1?xO2, where x is ?0.15 to 0.15, and M includes Mn and at least one element selected from the group consisting of Ni, Co, Al, Mg, Ti, Fe and Nb, with a lithium compound to obtain a mixture and calcining the mixture to obtain the over-lithiated layered lithium metal composite oxide.

Abstract: Disclosed is a Si-based alloy anode material for lithium ion secondary batteries, including an alloy phase with a Si principal phase including Si and a compound phase including two or more elements, which includes a first additional element A selected from Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Zr, Nb and Mg and a low-melting second additional element B selected from S, Se, Te, Sn, In, Ga, Pb, Bi, Zn, Al. This compound phase includes (i) a first compound phase including Si and the first additional element A; a second compound phase including the first additional element A and the second additional element B; and one or both of a third compound phase including two or more of the second additional elements B and a single phase of the second additional element B.

Abstract: An analytical cell includes first and second holders. The first and second holders each contain a substrate having a through-hole and a transmission membrane with an electron beam permeability so as to cover the through-hole. The first and second holders are stacked to form an overlapping portion such that the transmission membranes face each other. The through-holes face each other across the transmission membranes to form an observation window. Negative and positive electrode active materials are separated from each other and contact the electrolytic solution in the observation window. The negative and positive electrode active materials are electrically connected to negative and positive electrode collectors, respectively, in the overlapping portion. At least one of the negative and positive electrode collectors has an electrically insulating isolation membrane for avoiding contact with the electrolytic solution.

Abstract: A positive electrode active material is provided for an electric device that contains a first active material comprising a transition metal oxide represented by formula (1): Li1.5[NiaCobMnc[Li]d]O3 (where a, b, c, and d satisfy the relationships: 0<d<0.5; a+b+c+d=1.5; and 1.0<a+b+c<1.5); and a second active material comprising a spinel transition metal oxide that has a crystal structure assigned to the space group Fd-3m, represented by formula (2): LiMa?Mn2?a?O4 (where M indicates at least one metal element having an atomic valence of 2-4, and a? satisfies the relationship 0=a?<2.0). The fraction content of the first and second active material by mass ratio satisfies the relationship (3): 100:0 A:MB A indicates the mass of the first active material and MB indicates the mass of the second active material).

Abstract: The present invention relates to lithium composite compound particles having a composition represented by the formula: Li1+xNi1?y?zCoyMzO2 (M=B or Al), wherein the lithium composite compound particles have an ionic strength ratio A (LiO?/NiO2?) of not more than 0.3 and an ionic strength ratio B (Li3CO3+/Ni+) of not more than 20 as measured on a surface of the respective lithium composite compound particles using a time-of-flight secondary ion mass spectrometer. The lithium composite compound particles of the present invention can be used as a positive electrode active substance of a secondary battery which has good cycle characteristics and an excellent high-temperature storage property.

Abstract: An improved lithium-sulfur battery containing a surface-functionalized carbonaceous material. The presence of the surface-functionalized carbonaceous material generates weak chemical bonds between the functional groups of the surface-functionalized carbonaceous material and the functional groups of the polysulfides, which prevents the polysulfide migration to the battery anode, thereby providing a battery with relatively high energy density and good partial discharge efficiency.

Abstract: A fluoro material is provided for use as an electrode active material as well as a process tar producing it. The material includes particles of a fluorosulfate which corresponds to formula (I) L1-yFe1-xMnxSO4F (I) in which 0<x?1 and 0?y<1. The material includes a phase of triplite structure and optionally a phase of tavorite structure, the phase of triplite structure representing at least 50% by volume. The material may be obtained from precursors of the elements of which it is constituted, via a ceramic route, via an ionothermal route or via a polymer route.

Abstract: Regarding spinel-type lithium manganese-based composite oxide (LMO) to be used as a positive electrode active substance material for lithium battery, a novel LMO is provided, which is capable of maintaining discharge capacity even if charging and discharging are repeated under high temperatures. An LMO in which the crystallite size is 250 nm to 350 nm, the strain is 0.085 or less and the specific surface area increase rate when placed in water at 25° and pH 7 and ultrasonically dispersed at 40 W ultrasonic intensity for 600 seconds is 10.0% or less, can prevent a decrease in the output that accompanies the repetition of charging and discharging while at a high temperature.

Abstract: Disclosed is a transition metal precursor used for preparation of lithium composite transition metal oxide, the transition metal precursor comprising a composite transition metal compound represented by the following Formula 1: M(OH1?x)2?yAy/n??(1) wherein M comprises two or more selected from the group consisting of Ni, Co, Mn, Al, Cu, Fe, Mg, B, Cr and second period transition metals; A comprises one or more anions except OH1?x; 0?x?0.5; 0.01?y?0.5; and n is an oxidation number of A. The transition metal precursor according to the present invention contains a specific anion. A lithium composite transition metal oxide prepared using the transition metal precursor comprises the anion homogeneously present on the surface and inside thereof, and a secondary battery based on the lithium composite transition metal oxide thus exerts superior power and lifespan characteristics, and high charge and discharge efficiency.

Abstract: A coated substrate having an epoxy coating. The epoxy coating contains 4,5-dichloro-2-n-octylisothiazolin-3-one.

Abstract: The present invention provides a polycarbosilane represented by the following formula (1): [R1R2R3SiX1/2]M[R4R5SiX2/2]D[R6SiX3/2]T[SiX4/2]Q??(1); and a curable composition comprising: (A) said polycarbosilane of formula 1 as polycarbosilane A, (B) at least one polycarbosilane B represented by the following formula (2): [R7R8R9SiX1/2]M?[R10R11SiX2/2]D?[R12SiX3/2]T?[SiX4/2]Q?,??(2), and (C) at least a catalyst.

Abstract: A composition containing 4,5-dichloro-2-n-octylisothiazolin-3-one and an activated carbon having a surface area of at least 700 m2/g.

Abstract: A method of preparing an anode for a Li-ion Battery comprises mixing metal particles containing at least one of Ge, Sn and Si particles with carbon particles to form a mixture, and deoxidizing the metal particles by heating the mixture in a vacuum atmosphere in a range of 10?3 to 10?6 mbar for 60-100 hours at a temperature in a range of 150 to 350° C. to form a deoxidized mixture, the deoxidation improves the Li ion absorption performance of the anode.

Abstract: Methods for producing lithium iron phosphate or lithium manganese phosphate or lithium iron manganese phosphate, by colloidal synthesis are provided. Such methods include the operation of reacting a lithium salt, an iron(II) halide (and/or a manganese(II) halide) and a phosphorus compound, which, under the reaction conditions, is capable of releasing the phosphate ion, in the presence of an organic surfactant or a mixture of organic surfactants including an alkylamine or alkenylamine, in which the surfactant or mixture of surfactants is capable of dissolving the lithium salt and the iron halide (and/or the manganese halide), where used, in an organic solvent, which is liquid at room temperature, in which the surfactant or mixture of surfactants is soluble, the reaction being performed at a temperature not lower than 250° C.

Abstract: The present invention relates to a combustion method for producing a lithium insertion material for a cathode in a Li-ion battery, the material comprising iron, lithium, silicon, and carbon.

Abstract: A silicon/carbon composite comprises mesoporous silicon particles and carbon coating provided on the silicon particles, wherein the silicon particles have two pore size distribution of 2-4 nm and 20-40 nm. A process of preparing the silicon/carbon composite comprises the steps of preparing mesoporous silicon particles via a mechanochemical reaction between SiCl4 and Li33Si4 under ball milling and subsequent thermal treatment and washing process, and coating the mesoporous silicon particles with carbon. An anode for lithium ion battery comprises the silicon/carbon composite. A lithium ion battery comprises the silicon/carbon composite.

Abstract: A paste suitable for a negative plate of a lead-acid battery, the paste comprising lead oxide and carbon black, wherein the carbon black has the following properties: (a) a BET surface area between about 100 and about 2100 m2/g; and (b) an oil adsorption number (OAN) in the range of about 35 to about 360 cc/100 g, provided that the oil absorption number is less than the 0.14×the BET surface area+65.

Abstract: The present technology is able to provide a solid electrolyte cell that uses a positive electrode active material which has a high ionic conductivity in an amorphous state, and a positive electrode active material which has a high ionic conductivity in an amorphous state. The solid electrolyte cell has a stacked body, in which, a positive electrode side current collector film, a positive electrode active material film, a solid electrolyte film, a negative electrode potential formation layer and a negative electrode side current collector film are stacked, in this order, on a substrate. The positive electrode active material film is made up with an amorphous-state lithium phosphate compound that contains Li; P; an element M1 selected from Ni, Co, Mn, Au, Ag, and Pd; and O, for example.

Abstract: The invention is directed to a process for preparing a pulverulent compound of the formula NiaM1bM2cOx(OH)y where M1 is Fe, Co, Zn, Cu or mixtures thereof, M2 is Mn, Al, Cr, B, Mg, Ca, Sr, Ba, Si or mixtures thereof, having the following steps: a) providing at least a first starting solution and a second starting solution, b) combining of at least the first starting solution and the second starting solution in a reactor and producing a homogeneously mixed reaction zone having a specific mechanical power input of at least 2 watt/liter and producing a product suspension containing insoluble product and a mother liquor which is supersaturated by setting of an excess of alkali and has a pH of 10-12, c) partial separating the mother liquor from the precipitated product to set solids contents of at least 150 g/l in the suspension.

Abstract: Provided are methods and apparatus for forming electrode active materials for electrochemical cells. These materials include a metal (e.g., iron, cobalt), lithium, and fluorine and are produced using plasma synthesis or, more specifically, non-equilibrium plasma synthesis. A metal containing material, organometallic lithium containing material, and fluorine-containing material are provided into a flow reactor, mixed, and exposed to the electrical energy generating plasma. The plasma generation enhances reaction between the provided materials and forms nanoparticles of the electrode active materials. The nanoparticles may have a mean size of 1-30 nanometers and may have a core-shell structure. The core may be formed by metal, while the shell may include lithium fluoride. A carbon shell may be disposed over the lithium fluoride shell. The nanoparticles are collected and may be used to form an electrochemical cell.

Abstract: The present invention provides a multi-dimensional carbon active compound composite comprising a first carbon material, a second carbon material, an active compound, and further a seed material. This composite is capable of storing faradic or non-faradic charges. The produced multi-dimensional carbon can significantly inhibit the aggregation and disintegration of active compounds. Stacked carbon structure also formed a 3-D framework with high electron conductivity, which increases the rate capability of electrode. The green and simple synthesis process has a great potential for mass production. This green energy storage material can be widely applied to lithium secondary ion battery, supercapacitor, and lithium-air battery electrodes.

Abstract: Described is an electrode comprising and preferably consisting of electronically active material (EAM) in nanoparticulate form and a matrix, said matrix consisting of a pyrolization product with therein incorporated graphene flakes and optionally an ionic lithium source. Also described are methods for producing a particle based, especially a fiber based, electrode material comprising a matrix formed from pyrolized material incorporating graphene flakes and rechargeable batteries comprising such electrodes.

Abstract: A preparation method of a battery composite material includes steps of providing phosphoric acid, iron powder, a carbon source and a first reactant, processing a reaction of the phosphoric acid and the iron powder to produce a first product, calcining the first product to produce a precursor, among which the formula of the precursor is written by Fe7(PO4)6, and processing a reaction of the precursor, the carbon source and the first reactant to get a reaction mixture and calcining the reaction mixture to produce the battery composite material. As a result, the present invention achieves the advantages of reducing grind time of fabricating processes, so that the prime cost, the time cost, and the difficulty of fabricating are reduced.

Abstract: To obtain a non-aqueous electrolyte secondary battery having high capacity, high output and good cyclability, nickel manganese composite hydroxide particles are a precursor for a cathode active material having lithium nickel manganese composite oxide with a hollow structure and a small and uniform particle size. An aqueous solution for nucleation includes a metallic compounds that contains nickel and a metallic compound that contains manganese, but does not include a complex ion formation agent that forms complex ions with nickel, manganese and cobalt. After nucleation is performed, an aqueous solution for particle growth is controlled so that the temperature of the solution is 60° C. or greater, and so that the pH value that is measured at a standard solution temperature of 25° C. is 9.5 to 11.5, and is less than the pH value in the nucleation step.

Abstract: A lithium battery, including an anode, a cathode, an electrolyte solution and a package structure. The anode includes a material having an oxygen-containing functional group. The cathode and the anode are configured separately, and a housing region is defined between the cathode and the anode. The electrolyte solution is disposed in the housing region, and the electrolyte solution includes water and an additive. The package structure covers the anode, the cathode and the electrolyte solution.

Abstract: A redox flow battery. A metal-ligand coordination compound including an aromatic ligand that contains an electron withdrawing group is used as the catholyte and/or the anolyte so that a redox flow battery having high energy density and excellent charge/discharge efficiency may be provided.

Abstract: The amount of lithium ions that can be received and released in and from a positive electrode active material is increased, and high capacity and high energy density of a secondary battery are achieved. Provided is a lithium-manganese composite oxide represented by LixMnyMzOw, where M is a metal element other than Li and Mn, or Si or P, and y, z, and w satisfy 0?x/(y+z)<2, y>0, z>0, 0.26?(y+z)/w<0.5, and 0.2<z/y<1.2. The lithium manganese composite oxide has high structural stability and high capacity.

Abstract: Disclosed are mixed metal oxidized hydroxide precursors that can be used for the preparation of lithium mixed metal oxide cathode materials for secondary lithium ion batteries and methods of making such mixed metal precursors. The precursors typically are particles of nickel, cobalt, and manganese mixed metal oxidized hydroxides with varying metal molar ratios prepared in co-precipitation reactions in two sequential reactors.

Abstract: A method for producing an aqueous electrode paste includes charging a powder made of an active material and a thickener and an aqueous solvent inside of a two-shaft kneader, and, using the two-shaft kneader, thickly kneading the powder and the aqueous solvent to generate a mixture; and charging a misty aqueous solvent having an average liquid droplet diameter of 1 ?m or more and an average particle diameter (D50) of the thickener or less inside of the two-shaft kneader by spraying, and using the two-shaft kneader, diluting the mixture with the charged aqueous solvent.

Abstract: An all-solid state secondary cell which has a positive electrode active material layer, negative electrode active material layer, and solid electrolyte layer, wherein at least one of said positive electrode active material layer, said negative electrode active material layer, and said solid electrolyte layer includes an inorganic solid electrolyte and a binder comprised of an average particle size 30 to 300 nm particulate-shaped polymer and said particulate-shaped polymer is present in said positive electrode active material layer, said negative electrode active material layer, and said solid electrolyte layer in a state holding the particulate state, is provided.

Abstract: A material C-AxM(XO4)y that is of particles of a compound of the formula AxM(XO4)y, wherein said particles include a carbon deposit deposited by means of pyrolysis on at least a portion of the surface thereof, and where: A is Li alone or partially replaced by at most 10 atomic % of Na or K; M is Fe(II), or Mn(II), or mixtures thereof alone or partially replaced by at most 30 atomic % of one or more metals selected from Mn, Ni and Co and/or at most 5% of Fe(III); XO4 is PO4 alone or partially replaced by at most 10 molar % of at least one group selected from SO4, SiO4 and MoO4; and where said material has a calcium impurity content of lower than about 1000 ppm.

Abstract: Disclosed is rechargeable lithium battery that includes a positive electrode including a positive active material layer, a negative electrode including a negative active material and an electrolyte wherein the positive active material layer includes a positive active material, a binder, a conductive material, and an activated carbon, the activated carbon includes micropores in which manganese ions are adsorbed and trapped, and the activated carbon is included in an amount of about 0.1 wt % to about 3 wt % based on the total weight of the positive active material layer.

Abstract: The present disclosure relates to an electrochemical cell including an anode, a sulfur-containing cathode, a lithium-ion-containing electrolyte, and a porous carbon interlayer disposed between the anode and the cathode. The interlayer may be permeable to the electrolyte. The interlayer may be formed from a multiwall carbon nanotube (MWCNT) or a microporous carbon paper (MCP).

Abstract: A film using fullerene derivatives, a method for producing such films, and use of same are provided. In the film formed of hemispherical particles according to the present invention, the hemispherical particles are organized like a hexagonal close-packed structure, and are formed by specific fullerene derivatives. The hemispherical particles preferably have a bilayer membrane structure assembled to provide a flake-like surface for the hemispherical particles.