Abstract: An negative active material for a rechargeable lithium battery includes a nano-composite including a Si phase, a SiO2 phase, and a metal oxide phase of formulation MyO, where M is a metal with an oxidation number x, a free energy of oxygen-bond formation ranging from ?900 kJ/mol to ?2000 kJ/mol, x, and x·y=2. The negative active material for a rechargeable lithium battery according to the present invention can improve initial capacity, initial efficiency, and cycle-life characteristics by suppressing its initial irreversible reaction.

Abstract: A titanium suboxide powder comprising Ti4O7, Ti5O9 and Ti6O11, wherein the Ti4O7, Ti5O9 and Ti6O11 provide over 92% of the powder, and wherein the Ti4O7 is present at above 30% of the total powder.

Abstract: The invention provides an electrochemical cell which includes a first electrode having a electrode active material, a second electrode which is a counter electrode to the first electrode, and an electrolyte. The positive electrode active material is represented by the general formula AaVbNbc(PO4)3, wherein 0<a<9, and 0<b,c<2.

Abstract: A negative active material for a rechargeable lithium battery of the present invention includes a lithium-vanadium oxide core material being capable of performing reversible electrochemical oxidation and reduction, and an inorganic oxide coating layer disposed on the surface of the core material. The negative active material can improve stability at the interface between a negative electrode and an electrolyte, charge and discharge efficiency, and cycle-life, and can be applied along with all kinds of aqueous and non-aqueous binders.

Abstract: Field of use: the electrotechnical industry, in particular, anode materials for lithium-ion ECCs. Essence of the invention: Anode material based on lithium-titanium spinel that contains doping components, chromium and vanadium, in equivalent quantities, of the chemical formula Li4Ti5-2y(CryVy)O12-x, where x is the deviation from stoichiometry within the limits 0.02<x<0.5, and y is the stoichiometric coefficient within the limits 0<y<0.1.

Abstract: A cathode active material for a lithium secondary battery includes a lithium metal oxide secondary particle core formed by agglomerating lithium metal oxide primary particles; and a shell formed by coating the secondary particle core with barium titanate and metal oxide. This cathode active material allows making a lithium secondary battery having improved safety, particularly in thermal stability and overcharging characteristics.

Abstract: A secondary battery includes: a cathode including an active material; an anode; and an electrolytic solution. The active material has a composition represented by Formula (1) described below. A median diameter (D90) of the active material is from about 10.5 micrometers to about 60 micrometers both inclusive, the median diameter (D90) being measured by a laser diffraction method. A half bandwidth (2?) of a diffraction peak corresponding to a (020) crystal plane of the active material is from about 0.15 degrees to about 0.24 degrees both inclusive, the half bandwidth (2?) being measured by an X-ray diffraction method. LiaMnbFecMdPO4??(1) where M represents one or more of Mg, Ni, Co, Al, W, Nb, Ti, Si, Cr, Cu, and Zn; and 0<a?2, 0<b<1, 0<c<1, 0?d<1, and b+c+d=1 are established.

Abstract: A method of forming a polyanion active material that includes providing a carbon source, providing a mobile ion source, providing an active metal material, providing a network material, providing a flux material, and mixing the various materials. In one aspect, the mixing step may include grinding or pulverizing materials to a uniform fine mixture. In one aspect, a ball mill may be utilized to mix the components. Following the mixing of the materials, the mixture is heated to a predetermined temperature in a non-oxidizing atmosphere to form a reaction product. In one aspect, the mixture is heated to a temperature above a melting temperature of the flux material. In this manner, the flux material provides a medium in which the various reactants may react to form the desired reaction product. Following the heating of the mixture the reaction product is washed, forming a carbon coated polyanion active material.

Abstract: A composite anode active material including: a metal capable of alloy formation with lithium; an intermetallic compound; and a solid solution, in which the solid solution is an alloy of the metal capable of alloy formation with lithium and the intermetallic compound, and the solid solution and the intermetallic compound have a same crystal structure.

Abstract: For the purpose of increasing the electric capacity of lithium secondary batteries comprising titanium-based negative electrode materials, the present invention aims to produce a titanium oxide compound whose crystal structure, crystallite size, specific surface area and primary particle size are controlled, and to provide a lithium secondary battery comprising such a compound. The present invention produces a lithium secondary battery by using, as an electrode active material, a titanium oxide compound for use in an electrode, which is represented by TiO2.(H2O)a.(A2O)b (wherein A is Na or K, a is 0<a=1, and b is 0<b=0.1) and has a main peak at 2?=20° to 30° and a minor peak at 2?=45° to 55° in its X-ray diffraction pattern, wherein the crystallite size determined from the main peak ranges from 40 ? more to 500 ? or less.

Abstract: A negative electrode material for non-aqueous electrolyte secondary batteries, characterized in that the negative electrode material comprises a composite particle including solid phases A and B, the solid phase A being dispersed in the solid phase B, and the ratio (IA/IB) of the maximum diffracted X-ray intensity (IA) attributed to the solid phase A to the maximum diffracted X-ray intensity (IB) attributed to the solid phase B satisfies 0.001?IA/IB?0.1, in terms of a diffraction line obtained by a wide-angle X-ray diffraction measurement of the composite particle.

Abstract: An anode active material, an anode including the anode active material, a lithium battery including the anode, and a method of preparing the anode active material. The anode active material includes: a multilayer metal nanotube including: an inner layer; and an outer layer on the inner layer, wherein the inner layer includes a first metal having an atomic number equal to 13 or higher, and the outer layer includes a second metal different from the first metal.

Abstract: Methods for improving the electrical conductivity of a carbon felt material is provided. In some embodiments, a method improving the electrical conductivity of a carbon felt material comprises applying a carbon source liquid to at least a portion of a carbon felt material, optionally removing excess carbon source liquid from the carbon felt material, and converting the carbon source material to solid carbon, such as by heating. Also provided are materials and products created using these methods.

Abstract: The present invention is to provide an active material for a battery, which has high thermal stability and low electric potential. According to the invention, an active material for a battery comprising a M element in Group III, a Ti element, an O element, and a S element and having an M2Ti2O5S2 crystalline phase is provided to solve the problem.

Abstract: Disclosed herein is a cathode active material including a lithium manganese oxide, in which the lithium manganese oxide has a spinel structure with a predetermined constitutional composition represented by Formula 1 described in the detailed description, wherein a conductive material is applied to the surface of lithium manganese oxide particles, so as to exhibit charge-discharge properties in the range of 2.5 to 3.5V as well as in the 4V region.

Abstract: The present invention concerns a carbon coated lithium metal phosphate material containing a manganese oxide layer between the LiMnPO4 material or the C/LiMn1-x ZxPO4 material, where Z=Fe, Co, Ni, Mg, Ca, Al, Zr, V, Ti and x=0.01-0.3, and the carbon layer.

Abstract: A fabrication process for conformal coating of a thin polymer electrolyte layer on nanostructured electrode materials for three-dimensional micro/nanobattery applications, compositions thereof, and devices incorporating such compositions. In embodiments, conformal coatings (such as uniform thickness of around 20-30 nanometer) of polymer Polymethylmethacralate (PMMA) electrolyte layers around individual Ni—Sn nanowires were used as anodes for Li ion battery. This configuration showed high discharge capacity and excellent capacity retention even at high rates over extended cycling, allowing for scalable increase in areal capacity with electrode thickness. Such conformal nanoscale anode-electrolyte architectures were shown to be efficient Li-ion battery system.

Abstract: The present invention relates to electrode material for an electrical cell comprising as component (A) at least one ion- and electron-conductive metal chalcogenide, as component (B) carbon in a polymorph comprising at least 60% sp2-hybridized carbon atoms, as component (C) at least one sulfur-containing component selected from the group consisting of elemental sulfur, a composite produced from elemental sulfur and at least one polymer, a polymer comprising divalent di- or polysulfide bridges and mixtures thereof, and as component (D) optionally at least one binder. The invention further relates to a rechargeable electrical cell comprising at least one electrode which has been produced from or using the inventive electrode material, to the use of the rechargeable electrical cell and to the use of an ion- and electron-conductive metal chalcogenide for production of an inventive rechargeable electrical cell.

Abstract: An electrode and an electrode material for lithium electrochemical cells are disclosed. The electrode material is in powder form and has a particle size distribution wherein the measured particle size distribution of the electrode material has a median size D50 ranging from 1.5 ?m and 3 ?m, a D10?0.5 ?m, a D90?10.0 ?m, and a calculated ratio (D90/D10)/D50?3.0 which is indicative of a peak of the measured particle size distribution on the left of the median D50 which improves the loading and energy density of the electrode produced with this electrode material powder.

Abstract: An electrochemical device, having an anode containing magnesium; a cathode stable to a voltage of at least 3.2 V relative to a magnesium reference; and an electrolyte obtained by admixture of a magnesium salt of a non-nucleophilic base comprising nitrogen and aluminum trichloride in an ether solvent is provided. As sulfur is stable to a voltage of at least 3.2 V relative to a magnesium reference, a magnesium-sulfur electrochemical device is specifically provided.

Abstract: A process of electroless plating a tin or tin-alloy active material onto a metal substrate for the negative electrode of a rechargeable lithium battery comprising steps of (1) immersing the metal substrate in an aqueous plating solution containing metal ions to be plated, (2) plating tin or tin-alloy active material onto the metal substrate by contacting the metal substrate with a reducing metal by swiping one on the other, and (3) removing the plated metal substrate from the plating bath and rinsing with deionized water. A rechargeable lithium battery using tin or tin-alloy as the anode active material.

Abstract: The negative electrode for a rechargeable lithium battery includes a current collector and a negative active material layer disposed on the current collector. The negative active material layer includes a metal-based negative active material and sheet-shaped graphite and has porosity of 20 to 80 volume %. The negative electrode for a rechargeable lithium battery can improve cell characteristics by inhibiting volume change and stress due to active material particle bombardment during charge and discharge, and by decreasing electrode resistance.

Abstract: A nonaqueous electrolyte battery includes a positive electrode, a negative electrode containing a lithium-titanium composite oxide and a lithium-absorbing material in a weight ratio falling within the range defined in formula (1) given below, and a nonaqueous electrolyte. The lithium-absorbing material has a lithium absorption potential nobler than a lithium absorption potential of the lithium-titanium composite oxide. 3?(A/B)?100??(1) Where A denotes the weight (parts by weight) of the lithium-titanium composite oxide, and B denotes the weight (parts by weight) of the lithium-absorbing material.

Abstract: Active metal and active metal intercalation electrode structures and battery cells having ionically conductive protective architecture including an active metal (e.g., lithium) conductive impervious layer separated from the electrode (anode) by a porous separator impregnated with a non-aqueous electrolyte (anolyte). This protective architecture prevents the active metal from deleterious reaction with the environment on the other (cathode) side of the impervious layer, which may include aqueous or non-aqueous liquid electrolytes (catholytes) and/or a variety electrochemically active materials, including liquid, solid and gaseous oxidizers. Safety additives and designs that facilitate manufacture are also provided.

Abstract: Combinations of materials are described in which high energy density active materials for negative electrodes of lithium ion batteries. In general, metal alloy/intermetallic compositions can provide the high energy density. These materials can have moderate volume changes upon cycling in a lithium ion battery. The volume changes can be accommodated with less degradation upon cycling through the combination with highly porous electrically conductive materials, such as highly porous carbon and/or foamed current collectors. Whether or not combined with a highly porous electrically conductive material, metal alloy/intermetallic compositions with an average particle size of no more than a micron can be advantageously used in the negative electrodes to improve cycling properties.

Abstract: According to one embodiment, a negative electrode active material includes a compound having a crystal structure of monoclinic titanium dioxide. The compound has a highest intensity peak detected by an X-ray powder diffractometry using a Cu-K? radiation source. The highest intensity peak is a peak of a (001) plane, (002) plane, or (003) plane. A half-width (2?) of the highest intensity peak falls within a range of 0.5 degree to 4 degrees.

Abstract: A cathode composition and a rechargeable electrochemical cell comprising same are disclosed. The cathode composition is described as comprising (i) particles including a transition metal selected from the group consisting of Ni, Fe, Cr, Mn, Co, V, and combinations thereof; (ii) alkali halometallate; (iii) alkali halide; (iv) source of Zn; and (v) source of chalcogenide. Also described is a rechargeable electrochemical cell comprising the composition. The source of Zn and source of chalcogenide in the cathode composition of a cell may be effective to improve the extractable capacity of cells, and decrease the cell resistance, relative to their absence.

Abstract: A nonaqueous electrolyte battery includes a positive electrode, a negative electrode and a nonaqueous electrolyte. The negative electrode contains a lithium compound and a negative electrode current collector supporting the lithium compound. A log differential intrusion curve obtained when a pore size diameter of the negative electrode is measured by mercury porosimetry has a peak in a pore size diameter range of 0.03 to 0.2 ?m and attenuates with a decrease in pore size diameter from an apex of the peak. A specific surface area (excluding a weight of the negative electrode current collector) of pores of the negative electrode found by mercury porosimetry is 6 to 100 m2/g. A ratio of a volume of pores having a pore size diameter of 0.05 ?m or less to a total pore volume is 20% or more.

Abstract: A lithium-ion secondary battery includes a positive electrode, a negative electrode containing an active material, and an electrolytic solution, in which the active material includes a core portion capable of occluding and releasing lithium ions, and a covering portion arranged on at least part of a surface of the core portion, in which the covering portion contains, as constituent elements, Si, O, and at least one element M1 selected from Li, C, Mg, Al, Ca, Ti, Cr, Mn, Fe, Co, Ni, Cu, Ge, Zr, Mo, Ag, Sn, Ba, W, Ta, Na, and K, and the atomic ratio y (O/Si) of O to Si is 0.5?y?1.8.

Abstract: A lithium ion secondary battery is provided with a positive electrode, a negative electrode containing an active material, and an electrolytic solution, wherein the active material includes a core portion capable of occluding and releasing lithium ions, an amorphous or low-crystalline coating portion disposed on at least a part of the surface of the core portion, and a fibrous carbon portion disposed on at least a part of the surface of the coating portion, and the coating portion contains Si and O as constituent elements, while the atomic ratio y (O/Si) of O relative to Si satisfies 0.5?y?1.8.

Abstract: A lithium-ion secondary battery includes a positive electrode, a negative electrode containing an active material, and an electrolytic solution, in which the active material contains, as constituent elements, Si, O, and at least one element Ml selected from Li, C, Mg, Al, Ca, Ti, Cr, Mn, Fe, Co, Ni, Cu, Ge, Zr, Mo, Ag, Sn, Ba, W, Ta, Na, and K, and the atomic ratio x (O/Si) of O to Si is 0.5?x?1.8.

Abstract: Compositions, and methods of obtaining them, useful for lithium ion batteries comprising discrete oxidized carbon nanotubes having attached to their surface lithium ion active materials in the form of nanometer sized crystals or layers. The composition can further comprise graphene or oxygenated graphene.

Abstract: According to one embodiment, there is provided a nonaqueous electrolyte battery including a positive electrode, a negative electrode, and a nonaqueous electrolyte. The negative electrode includes a first negative electrode active material containing a monoclinic ?-type titanium composite oxide and a second negative electrode active material. The second negative electrode active material causes insertion and release of lithium ion in a potential range from 0.8 V to 1.5 V (vs. Li/Li+).

Abstract: A battery includes a cathode, an anode, and an aqueous electrolyte disposed between the cathode and the anode and including a cation A. At least one of the cathode and the anode includes an electrode material having an open framework crystal structure into which the cation A is reversibly inserted during operation of the battery. The battery has a reference specific capacity when cycled at a reference rate, and at least 75% of the reference specific capacity is retained when the battery is cycled at 10 times the reference rate.

Abstract: A negative electrode active material contains a metal-displaced lithium-titanium oxide of a ramsdellite structure expressed by the formula Li(16/7)?xTi(24/7)?yMyO8 (where M is at least one metal element selected from the group consisting of Nb, Ta, Mo, and W, and x and y are respectively numbers in the range of 0<x<16/7 and 0<y<24/7).

Abstract: Provided are a cathode and a lithium battery including the cathode. The cathode includes a cathode active material that includes an oxide represented by the following Formula 1: LixNi0.5+y(Mn1-z1-z2Mz1Moz2)0.5?yO2,??<Formula 1> wherein 0.9<x<1.2, ?0.02<y<0.2, 0.001<z1<0.5, 0.001<z2<0.5, and M is a metallic atom having an oxidation number of +2.

Abstract: A nano graphene-enabled vanadium oxide composite composition for use as a lithium battery cathode active material, wherein the composite composition is formed of one or a plurality of graphene, graphene oxide, or graphene fluoride sheets or platelets and a plurality of nano-particles, nano-rods, nano-wires, nano-sheets, and/or nano-belts of a vanadium oxide with a size smaller than 100 nm (preferably smaller than 20 nm, further preferably smaller than 10 nm, and most preferably smaller than 5 nm), and wherein the graphene, graphene oxide, or graphene fluoride (having a thickness <20 nm, preferably <10 nm, further preferably <5 nm, and being most preferably of single-layer or less than 5 layers) is in an amount of from 0.01% to 50% (preferably <10%) by weight based on the total weight of graphene, graphene oxide or graphene fluoride and the vanadium oxide combined.

Abstract: Conductor for an electrode of an electrochemical energy storage means, in particular of, essentially, prismatic shape, with a passage region through which electrons may enter into the conductor or through which electrons may exit from the conductor.

Abstract: According to one embodiment, a nonaqueous electrolyte secondary battery is provided. The battery comprises a positive electrode includes a lithium-nickel complex oxide, a negative electrode includes a lithium-titanium complex oxide and a lithium-containing phosphorous oxide, and a nonaqueous electrolyte.

Abstract: A negative active material for a rechargeable lithium battery that includes a core including a compound represented by the following Chemical Formula 1, and a carbon layer disposed on the core and including low crystalline carbon. LixTiyOz ??[Chemical Formula 1] where 0.1?x?4, 1?y?5, and 2?z?12.

Abstract: A coin-type lithium secondary battery includes a positive electrode, a negative electrode, a separator interposed between the positive electrode and the negative electrode, and a non-aqueous electrolyte. The negative electrode includes a negative electrode active material including a silicon alloy material, a conductive agent including a carbon material, and a binder. The silicon alloy material includes a phase A including a lithium-silicon alloy and a phase B including an intermetallic compound of a transition metal element and silicon. In the lithium-silicon alloy, a ratio of lithium atoms relative to silicon atoms is 2.75 to 3.65 in a 100% state-of-charge.

Abstract: Provided are an anode for a battery comprising: (a) an anode active material, (b) TiO2, and (c) a styrene-butadiene rubber (SBR), and a lithium secondary battery comprising the same. By using titanium oxide and SBR together with an anode active material as the anode components in the present invention, increase in the anode resistivity during the high-temperature storage and reduction in the battery capacity by the resistivity are inhibited, thereby the overall performances of the battery can be improved.

Abstract: Disclosed is an electrical storage device having excellent safety and high battery capacity. Specifically disclosed is an electrical storage device comprising at least a positive electrode having a positive electrode active material layer and a positive electrode collector, a negative electrode having a negative electrode active material layer and a negative electrode collector, a separator and an organic electrolyte solution. This electrical storage device is characterized in that the negative electrode active material layer is composed of a metal complex oxide which absorbs and desorbs lithium ions, the positive electrode active material layer contains a carbonaceous material having a layered crystal structure, and the interlayer distance d002 of the layered crystal structure in the carbonaceous material is within the range of 0.36-0.38 nm.

Abstract: A solid vanadium rechargeable battery, including; a first vanadium compound containing vanadium, whose oxidation number changes between 2 and 3 due to oxidation and reduction reactions, or solid vanadium salt or complex salt including such vanadium, and a surface that becomes a negative electrode; a second vanadium compound containing vanadium, whose oxidation number changes between 5 and 4 due to reduction and oxidation reactions, or solid vanadium salt or complex salt including such vanadium, and a surface that becomes a positive electrode; and a separator sandwiched between the first and the second vanadium compounds for selectively allowing ions to pass through, is provided.

Abstract: A lithium ion secondary battery includes a positive electrode, a negative electrode, and an electrolytic solution. The positive electrode contains a lithium composite oxide. The negative electrode contains a material including at least one of silicon Si and tin Sn as a constituent element. The lithium composite oxide includes lithium Li having a composition ratio a, a first element having a composition ratio b, and a second element having a composition ratio c as a constituent element. The first element including two kinds or more selected from among manganese Mn, nickel Ni, and cobalt Co, and including at least manganese. The second element including at least one kind selected from among aluminum Al, titanium Ti, magnesium Mg, and boron B. The composition ratios a to c satisfy the relationships of 1.1<a<1.3, 0.7<b+c<1.1, 0<c<0.1, and a>b+c.

Abstract: The present invention is directed to a method for making electrode active materials represented by the general formula: Aa(VO)bXO4, wherein: (a) A is an alkali metal or mixture of alkali metals, and 0<a<4; (b) 0<b<2; (c) X is selected from the group consisting of phosphorous (P), sulfur (S), arsenic (As), silicon (Si), and combinations thereof; and wherein A, X, a and b are selected to maintain the electroneutrality of the electrode active material in its nascent (as prepared or synthesized) state.

Abstract: Disclosed is a secondary battery with a non-aqueous electrolyte that has excellent cycle characteristics and output characteristics. Also disclosed is a positive electrode active material for a secondary battery with a non-aqueous electrolyte that includes a powder of a volume resistivity of 20 ?·cm or more and 100 ?·cm or less when said powder has a bulk density of 3 g/cm3. The use of the lithium nickel composite oxide as a positive electrode active material can provide a secondary battery with a non-aqueous electrolyte that has excellent cycle characteristics and output characteristics.

Abstract: A nonaqueous electrolyte battery, containing a case and provided in the case, a positive electrode, a negative electrode and a nonaqueous electrolyte. The negative electrode comprises a lithium-titanium composite oxide, wherein a crystallite diameter of the lithium-titanium composite oxide is not larger than 6.9×102 ?. The lithium-titanium composite oxide comprises: rutile TiO2; anatase TiO2; Li2TiO3; and a lithium titanate having a spinel structure. A main peak intensity relative to lithium titanate set at 100, as determined by X-ray diffractometry, of each of lithium titanate having a spinel structure, the rutile TiO2, the anatase TiO2 and Li2TiO3 is not larger than 7.

Abstract: A negative electrode for a lithium battery includes an active material layer and a current collector. The active material layer has a plurality of crystal grains and the plurality of crystal grains include a plurality of pores. A first pore of the plurality of pores has a first length and a second length, the first length being the maximum length orthogonal to the current collector and the second length being the maximum length orthogonal to the first length, and the first length is greater than the second length.

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.