Abstract: A lithium-ion secondary battery comprises a negative electrode active material, a positive electrode active material, and an electrolytic solution. The negative electrode active material contains elemental silicon or a silicon-containing alloy. The electrolytic solution has a lithium salt and a solvent. The solvent contains a cyclic carbonate, a chain carbonate, fluoroethylene carbonate represented by the formula (1), and 1,3-propane sultone. In the electrolytic solution, fluoroethylene carbonate has a mass concentration Cf of 0.1 to 3 mass %, 1,3-propane sultone has a mass concentration Cp of 0.1 to 3 mass %, and Cf>Cp.

Abstract: An anode active material for a lithium secondary battery having a high capacity and a high efficiency of charge discharge characteristics. The anode active material includes a silicon mono-phase and an alloy phase formed of silicon with a metal element at least one selected from the group consisting of Ti, Ni, Cu, Fe, Mn, Al, Cr, Co, and Zn. The anode active material is a powder in which the silicon mono-phase is uniformly distributed in a matrix of the alloy phase, has particle size distribution defined as D0.1 and D0.9, and the value of D0.1-D0.9 is in a range from about 3 ?m to about 15 ?m.

Abstract: A lithium ion secondary battery includes: a positive electrode; a negative electrode; and an electrolytic solution, at least one of the positive electrode and the negative electrode being capable of storing and releasing lithium ions, and containing an active material that satisfies predetermined conditions.

Abstract: According to one embodiment, an active material includes an element M and a monoclinic crystal structure represented by the formula TiNb2O7. The element M includes at least one element selected from the group consisting of Mg, Ca, Sr, Ba, Pb, and P.

Abstract: A lithium ion conductor represented by Formula 1: Li1+x+2yAlxMgyM2?x?y(PO4)3 ??Formula 1 wherein, in Formula 1, M includes at least one of titanium (Ti), germanium (Ge), zirconium (Zr), hafnium (Hf), and tin (Sn), 0<x<0.6, and 0<y<0.2.

Abstract: Disclosed are a positive electrode for a rechargeable lithium battery and a rechargeable lithium battery including the same, and the positive electrode includes a current collector; and a positive active material layer including an additive which is LixV2O5 (1<x<4) or a composite of LixV2O5 (1<x<4) and metal oxide, and a positive active material, and being disposed on the current collector.

Abstract: The present invention relates to negative electrode materials for rechargeable lithium batteries and to rechargeable lithium batteries including the same. The negative electrode materials improve the capacity characteristics and cycle-life characteristics of the rechargeable lithium batteries. The negative electrode material includes a negative active material capable of intercalating and deintercalating lithium ions, and the negative active material includes an oxide particle represented by LixMyVzO2+d and having a full width at half maximum of a X-ray diffraction angle (2?) at a (003) plane of 0.2 degrees or more as measured by X-ray diffraction analysis using a CuK?ray.

Abstract: A lithium-ion battery is provided that has a fast charge and discharge rate capability and low rate of capacity fade during high rate cycling. The battery can exhibit low impedance growth and other properties allowing for its use in hybrid electric vehicle applications and other applications where high power and long battery life are important features.

Abstract: Provided are examples of electrochemically active electrode materials, electrodes using such materials, and methods of manufacturing such electrodes. Electrochemically active electrode materials may include a high surface area template containing a metal silicide and a layer of high capacity active material deposited over the template. The template may serve as a mechanical support for the active material and/or an electrical conductor between the active material and, for example, a substrate. Due to the high surface area of the template, even a thin layer of the active material can provide sufficient active material loading and corresponding battery capacity. As such, a thickness of the layer may be maintained below the fracture threshold of the active material used and preserve its structural integrity during battery cycling.

Abstract: Energy storage devices having hybrid anodes can address at least the problems of active material consumption and anode passivation that can be characteristic of traditional batteries. The energy storage devices each have a cathode separated from the hybrid anode by a separator. The hybrid anode includes a carbon electrode connected to a metal electrode, thereby resulting in an equipotential between the carbon and metal electrodes.

Abstract: The present invention relates to a cathode active material for a lithium secondary battery comprising: a core including a compound represented by chemical formula 1, and a shell including a compound represented by chemical formula 2, wherein the material composition of the core and the material composition of the shell are different; and a lithium secondary battery including the cathode active material for a lithium secondary battery.

Abstract: To provide nickel composite hydroxide particles having a small and uniform particle diameter and a method for producing the same. The method for producing the nickel composite hydroxide particles includes: a nucleation step of producing nuclei including primary particles by controlling a pH of an aqueous solution for nucleation to 11.5 to 13.2 at a liquid temperature of 25° C., the aqueous solution for nucleation containing a metal compound having an atomic ratio of metals corresponding to an atomic ratio of metals in the nickel composite hydroxide particles and substantially not containing a metal complex ion-forming agent; and a particle growth step of forming, on an outer surface of each of the nuclei, an outer shell portion including platy primary particles larger than primary particles of the nuclei by controlling a pH of an aqueous solution for particle growth containing the nuclei obtained in the nucleation step to 9.5 to 11.0 at a liquid temperature of 25° C.

Abstract: (A) A cathode active material of a cathode includes a lithium phosphate compound represented by LiaM1bPO4 (M is Fe and the like, 0?a?2, b?1). (B) Fine pore distribution of the cathode measured by a mercury intrusion method indicates a peak P1 in a range where a pore diameter is equal to or more than about 0.01 micrometers and less than about 0.15 micrometers, and indicates a peak P2 in a range where the pore diameter is from about 0.15 micrometers to about 0.9 micrometers both inclusive. (C) A ratio I2/I1 between intensity I1 of the peak P1 and intensity I2 of the peak P2 is from about 0.5 to about 20 both inclusive. (D) Porosity of the cathode is from about 30 percent to about 50 percent both inclusive.

Abstract: According to one embodiment, there is provided a non-aqueous electrolyte secondary battery including a positive electrode including a positive electrode active material layer, a negative electrode including a negative electrode active material layer, and a non-aqueous electrolyte. At least one of the positive electrode active material layer and the negative electrode active material layer contains carbon dioxide and releases the carbon dioxide in the range of 0.1 ml to 10 ml per 1 g when heated at 350° C. for 1 minute.

Abstract: The invention provides electrode active materials comprising lithium or other alkali metals, manganese, a +3 oxidation state metal ion, and optionally other metals, and a phosphate moiety. Such electrode active materials include those of the formula: AaMnbMIcMIIdMIIIePO4 wherein (a) A is selected from the group consisting of Li, Na, K, and mixtures thereof, and 0<a?1; (b) 0<b?1; (c) MI is a metal ion in the +3 oxidation state, and 0<c<0.5; (d) MII is metal ion, a transition metal ion, a non-transition metal ion or mixtures thereof, and 0?d<1; (e) MIII is a metal ion in the +1 oxidation state and 0<e<0.5; and wherein A, Mn, MI, MII, MIII, PO4, a, b, c, d and e are selected so as to maintain electroneutrality of said compound.

Abstract: According to one embodiment, there is provided an active material including a titanium oxide compound having a monoclinic titanium dioxide crystal structure and satisfying the equation (I). S1/(S2+S3)?1.9??(I). In the above equation, S1 is the peak area of a peak existing in a wavelength range from 1430 cm?1 to 1460 cm?1, S2 is the peak area of a peak existing in a wavelength range from 1470 cm?1 to 1500 cm?1, and S3 is the peak area of a peak existing in a wavelength range from 1520 cm?1 to 1560 cm?1, in the infrared diffusion reflective spectrum of the active material after pyridine is absorbed and then released.

Abstract: A positive electrode active material for a nonaqueous electrolyte battery. The positive electrode active material has been manufactured through a mixing step and a heating step. In the mixing step, a mixture is produced by mixing niobium pentoxide (Nb2O5) with lithium hydroxide (LiOH) at a molar ratio of 1:1. In the heating step, the mixture is heated in an atmosphere of air at substantially 800° C. The positive electrode active material having been produced through the mixing process and the heating process causes the plateau potential in a discharge to be approximately 1.0 [V] for lithium. And the nonaqueous electrolyte battery using the positive electrode active material can operate at a voltage of approximately 1.0 [V].

Abstract: The present invention provides a lithium-sulfur battery using a solid high-ionic conductor in a three-dimensional (3D) porous structure. In particular, at a higher temperature (120° C. or higher) than a melting temperature, the lithium-sulfur battery does not have fluid sulfur leaking outside of a battery cell electrode. The lithium-sulfur battery can be operated at both a high temperature and room temperature. The battery of the invention can be used without performance degradation and with increased ion conductivity at a high temperature, thus improving the battery's power performance.

Abstract: A secondary electrochemical cell comprises an anode, a cathode including electrochemically active cathode material, a separator between the anode and the cathode, and an electrolyte. The electrolyte comprises at least one salt dissolved in at least one organic solvent. The separator in combination with the electrolyte has an area-specific resistance of less than about 2 ohm-cm2.

Abstract: A nonaqueous electrolyte secondary battery including a negative electrode containing a graphite material as the negative active material, a positive electrode containing lithium cobalt oxide as a main component of the positive active material and a nonaqueous electrolyte solution, the battery being characterized in that the lithium cobalt oxide contains a group IVA element selected from the group consisting of Ti, Zr and Hf and a group IIA element of the periodic table, the nonaqueous electrolyte solution contains 0.2-1.5% by weight of a sulfonyl-containing compound and preferably further contains 0.5-4% by weight of vinylene carbonate.

Abstract: The invention relates to a lithium battery including a cell comprising: a positive electrode, a negative electrode, and an electrolyte consisting of an aqueous solution of a lithium salt, characterized in that the electrolyte has a pH of at least 14, the positive electrode has a lithium intercalation potential greater than 3.4 V, and the negative electrode has a lithium intercalation potential less than 2.2 V.

Abstract: A lithium-sulfur cell comprising an anode structure, a cathode structure and an electrolyte section abutting to the cathode structure. The cathode structure comprises a continuous layer of nanotubes or nanowires and sulfur particles. The sulfur particles are attached to the nanotubes or nanowires. The continuous layer of nanotubes or nanowires abuts to at least a part of the electrolyte section. The invention further relates to a corresponding method for manufacturing the inventive cell.

Abstract: The object of the present invention is to provide a method for producing lithium transition metal phosphate with a small particle size and uniform element spatial distribution, which enables continuous and large-scale synthesis. Its solution is as follows: A particulate mixture is synthesized by the spray-combustion method, wherein a mixed solution containing a lithium source, a transition metal source, and a phosphorus source is supplied into a flame along with a combustion-supporting gas and a flammable gas, as a mist-like droplet. It is a method for producing lithium transition metal phosphate-type cathode active material, which further comprises a process of mixing the synthesized particulate mixture with a carbon source, a process of calcining the particulate mixture under inert gas atmosphere to produce an active material aggregate, and a process of pulverizing the active material aggregate.

Abstract: A nanosized particle has a first phase that is a simple substance or a solid solution of element A, which is Si, Sn, Al, Pb, Sb, Bi, Ge, In or Zn, and a second phase that is a compound of element D, which is Fe, Co, Ni, Ca, Sc, Ti, V, Cr, Mn, Sr, Y, Zr, Nb, Mo, Ru, Rh, Ba, lanthanoid elements (not including Ce and Pm), Hf, Ta, W or Ir, and element A, or a compound of element A and element M, which is Cu, Ag, or Au. The first phase and second phase are bound via an interface, and are exposed to the outer surface. The surface of the first phase other than the interface is approximately spherical. Furthermore, a lithium ion secondary battery includes the nanosized particle as an anode active material.

Abstract: A method for producing a lithium mixed metal oxide, which includes mixing a lithium compound, metallic Ni or a compound thereof, and one or more transition metals selected from the group consisting of Mn, Co, Ti, Cr and Fe or a compound thereof; and calcining the obtained raw material mixture under an atmosphere of the concentration of carbon dioxide of from 1% by volume to 15% by volume at 630° C. or higher.

Abstract: An object of the present invention is to simplify the process of producing an electrode composite material. Disclosed is a method for producing an electrode composite material, comprising the steps of: preparing a material comprising Li, La, Ti and O and heating the material, wherein the composition ratio between Li, La and Ti of the material is in the range of a triangle having three vertices at LiO0.5:LaO1.5:TiO2=23:24:53, LiO0.5:LaO1.5:TiO2=5:36:59 and LiO0.5:LaO1.5:TiO2=8:28:64 in the LiO0.5—LaO1.5—TiO2 triangular diagram.

Abstract: A lithium titanium oxide for an anode active material of a lithium rechargeable battery, wherein a X-ray diffraction (XRD) spectrum has a first peak of Li4Ti5O12 and a second peak, and A50-55/A78-80 is in a predetermined range, as a result of XRD analysis, where A78-80 is an Area of the first peak and A50-55 is an Area of the second peak in XRD.

Abstract: There are provided a Si alloy powder for a lithium ion secondary battery negative electrode active material, which has a high discharge capacity and excellent cycle life, and a method for producing the same. The Si alloy powder of the present invention comprises a eutectic structure including a Si phase and a CrSi2 phase, and the average value of thicknesses in a thin width direction in each phase of the Si phase and the CrSi2 phase is 4 ?m or less. This Si alloy powder is produced by quenching and solidifying a dissolution material which gives the composition of the Si alloy powder at a cooling rate of 100° C./s or more.

Abstract: Provided is a nonaqueous electrolyte battery that has a high capacity and a high volume power density and can have an enhanced charge-discharge cycle capability. The nonaqueous electrolyte battery includes a positive-electrode layer, a negative-electrode layer, and a solid-electrolyte layer disposed between these layers. The negative-electrode layer contains a powder of a negative-electrode active material and a powder of a solid electrolyte. In the negative-electrode active material, a charge-discharge volume change ratio is 1% or less and the powder has an average particle size of 8 ?m or less. The solid-electrolyte layer is formed by a vapor-phase process. Examples of the negative-electrode active material having a charge-discharge volume change ratio of 1% or less include Li4Ti5O12 and non-graphitizable carbon.

Abstract: In one aspect, a composite cathode active material including at least one large-diameter active material, and at least one small-diameter active material, a cathode including the composite cathode active material and a lithium battery including the cathode is provided.

Abstract: A cathode active material includes a lithium metal phosphate represented by Formula 1; and one or more compounds selected from the group consisting of a metal oxynitride, a metal nitride, and a mixture thereof: LiMPO4??<Formula 1> where M is selected from the group consisting of Fe, Ti, V, Cr, Co and Ni.

Abstract: The present invention provides a novel titanium-based composite oxide being usable as an electrode material for a lithium secondary battery and having a high capacity and an excellent cycle stability, a method for producing the same and a lithium secondary battery using the titanium-based composite oxide. Disclosed is a compound obtained by compositing titanium oxide with elements other than titanium, specifically a titanium-based composite oxide wherein the relevant chemical formula is Ti(1-x)MxOy, M is the element Nb or the element P, or a combination of these two elements in an optional ratio therebetween, x is such that 0<x<0.17, y is such that 1.8?y?2.1, x is the sum of Nb and P when M is a combination of the element Nb and the element P, and the present invention provides a lithium secondary battery using as an electrode the titanium-based composite oxide.

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: Since pseudo-capacitance transition metal oxides (for example, MnO2) have high theoretical capacitance and are eco-friendly, inexpensive, and abundant in the natural world, pseudo-capacitance transition metal oxides are gaining attention as promising capacitor electrode materials. However, pseudo-capacitance transition metal oxides have relatively low electronic conductivity and limited charging and discharging rates, and a it is therefore difficult to use pseudo capacitance transition metal oxides for high output power applications. If a plating process accompanying a liquid-phase precipitation reaction is performed on a nanoporous metal such as nanoporous gold (NPG) to deposit a ceramic material (for example, MnO2 or SnO2) on the surface of a core metal (for example, NPG), a nanoporous metal-ceramic composite having particular structural characteristics and comprising a metal core part and a ceramic deposition part can be obtained.

Abstract: Li—Ni composite oxide particles for a non-aqueous electrolyte secondary battery with a large charge/discharge capacity and excellent thermal stability in a charged condition. The Li—Ni composite oxide secondary particles form core particles having a composition Lix1Ni1-y1-z1-w1Coy1Mnz1Mw1O2 in which 0.9?x1?1.3; 0.1?y1?0.3; 0.0?z1?0.3; 0?w1?0.1; and M is Al or Fe. The Li—Ni composite oxide has a composition Lix2Ni1-y2-z2-w2Coy2Mnz2Mw2O2 in which 0.9?x2?1+z2; 0?y2?0.33; 0?z2?0.5; 0?w2?0.1; and M is Al, Fe, Mg, Zr or Ti and is coated or present on a surface of the secondary particles.

Abstract: Provided are negative electrode compositions for lithium-ion electrochemical cells that include metal oxides and polymeric binders. Also provided are electrochemical cells and battery packs that include electrodes made with these compositions.

Abstract: The invention provides a method for producing a carbon material as a negative electrode active material that can dope and undope a sodium ion. The production method of a carbon material for a sodium secondary battery includes a step of heating at a temperature of 800 to 2500° C. a compound according to Formula (1), Formula (2) or Formula (3), and having 2 or more oxygen atoms, or a mixture of an aromatic derivative 1 having an oxygen atom in the molecule and an aromatic derivative 2 having a carboxyl group in the molecule and being different from the aromatic derivative 1.

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: Disclosed is to a method of manufacturing an anode active material, including mixing a first solution having a metal oxide precursor dissolved therein, a second solution having a polymer as a carbon fiber precursor dissolved therein, and an ionic liquid solution for nitrogen doping and formation of a porous structure, thus preparing an electrospinning solution, electrospinning the electrospinning solution, thus preparing a metal oxide-nitrogen-porous carbon nanofiber composite, and thermally treating the composite, and to an anode and a lithium battery using the anode active material.

Abstract: Nanocomposite materials having at least two layers, each layer consisting of one metal oxide bonded to at least one graphene layer were developed. The nanocomposite materials will typically have many alternating layers of metal oxides and graphene layers, bonded in a sandwich type construction and will be incorporated into an electrochemical or energy storage device.

Abstract: According to one embodiment, a negative electrode active material for a nonaqueous electrolyte battery is provided. The active material includes a titanium oxide compound having a crystal structure of a monoclinic titanium dioxide and having a crystallite, the crystallite having a crystallite size of 5 to 25 nm when it is calculated by using the half width of the peak of a (110) plane obtained by a powder X-ray diffraction (XRD) method using a Cu—K? ray.

Abstract: A secondary battery includes: a fiber negative electrode having a surface on which a negative electrode active material coating is formed, the coating containing a compound of AaMbXcZd; a fiber positive electrode including a positive electrode active material coating containing nickel hydroxide; an aqueous electrolyte solution; and a separator. The negative electrode coating has an uncoated surface. A is selected from the group consisting of Li, Na, K, Rb, Cs, Be, Mg, Ca, Sr, and Ba; M is selected from the group consisting of Ti, V, Cr, Mn, Fe, Co, Ni, Cu, Nb, Mo, Ru, Pd, Ag, Ta, W, Pr, Sm, Eu, and Pb; X is selected from the group consisting of B, Al, Si, P, S, Ga, and Ge; Z is selected from the group consisting of O, S, N, F, Cl, Br, and I; and 0?a?6, 1?b?5, 0?c?4, 0<d?12, and 0?a/b?4.

Abstract: An electrode, including a polymer matrix and a plurality of graphene-vanadium pentoxide composite materials dispersed in the polymer matrix. Each respective graphene-vanadium pentoxide particle includes a vanadium pentoxide substrate wrapped in a respective graphene monolayer sheet, each respective monolayer sheet is bonded to a respective vanadium pentoxide substrate, and wherein each respective vanadium pentoxide substrate is about 1 to about 100 nm long.

Abstract: Provided is an all solid state battery which has the same level of discharge capacity as in the case of using an electrolyte solution, and is able to improve the cycle stability. An all solid state battery includes a solid electrolyte layer, as well as a positive electrode layer and a negative electrode layer provided in positions opposed to each other with the solid electrolyte layer interposed therebetween. At least one of the positive electrode layer and the negative electrode layer is bonded to the solid electrolyte layer by firing. The negative electrode layer contains an electrode active material composed of a metal oxide containing no lithium, and a solid electrolyte containing no titanium.

Abstract: This invention relates generally to electrode materials, electrochemical cells employing such materials, and methods of synthesizing such materials. The electrode materials have a crystal structure with a high ratio of Li to metal M, which is found to improve capacity by enabling the transfer of a greater amount of lithium per metal, and which is also found to improve stability by retaining a sufficient amount of lithium after charging. Furthermore, synthesis techniques are presented which result in improved charge and discharge capacities and reduced particle sizes of the electrode materials.

Abstract: A positive electrode is disclosed for a non-aqueous electrolyte lithium rechargeable cell or battery. The electrode comprises a lithium containing material of the formula NayLixNizMn1-z-z?Mz?Od, wherein M is a metal cation, x+y>1, 0<z<0.5, 0?z?<0.5, y+x+1 is less than d, and the value of d depends on the proportions and average oxidation states of the metallic elements, Li, Na, Mn, Ni, and M, if present, such that the combined positive charge of the metallic elements is balanced by the number of oxygen anions, d. The inventive material preferably has a spinel or spinel-like component in its structure. The value of y preferably is less than about 0.2, and M comprises one or more metal cations selected preferably from one or more monovalent, divalent, trivalent or tetravalent cations, such as Mg2+, Co2+, Co3+, B3+, Ga3+, Fe2+, Fe3+, Al3+, and Ti4+.

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: An all-solid-state battery includes: a positive electrode active material layer that contains a positive electrode active material, and a first sulfide solid electrolyte material that contacts the positive electrode active material and that substantially does not have a cross-linking chalcogen; a negative electrode active material layer containing a negative electrode active material; and a solid electrolyte layer that is provided between the positive electrode active material layer and the negative electrode active material layer, and that contains a second sulfide solid electrolyte material that substantially has a cross-linking chalcogen.

Abstract: Nanocomposite materials comprising a metal oxide bonded to at least one graphene material. The nanocomposite materials exhibit a specific capacity of at least twice that of the metal oxide material without the graphene at a charge/discharge rate greater than about 10 C.

Abstract: A method for forming a nanocomposite material, the nanocomposite material formed thereby, and a battery made using the nanocomposite material. Metal oxide and graphene are placed in a solvent to form a suspension. The suspension is then applied to a current collector. The solvent is then evaporated to form a nanocomposite material. The nanocomposite material is then electrochemically cycled to form a nanocomposite material of at least one metal oxide in electrical communication with at least one graphene layer.