Abstract: A negative electrode active material includes a hydrogen storage alloy. The hydrogen storage alloy has an A2B7 crystal structure. The hydrogen storage alloy includes nickel. The saturation magnetization per unit mass is 1.9 emu·g?1 or more.

Abstract: To provide an anode material that can improve the efficiency of the initial charging and discharging, the anode material includes an amorphous glassy carbon material that is an anode active material, and a NaMH compound that is a solid electrolyte.

Abstract: A data management system includes a data management device and an arithmetic device. The data management device is configured to acquire battery data and store, in a distributed ledger, transaction data including information on the acquired battery data. The arithmetic device is configured to acquire the battery data from the data management device and calculate an index using the battery data and a predetermined arithmetic formula. The arithmetic device is configured to offer the index to a disclosure server.

Abstract: A hydrogen storage alloy suitable for a negative electrode of an on-board alkaline storage battery, an alkaline storage battery using this hydrogen storage alloy, and a vehicle; wherein a fine-grained hydrogen storage alloy is used for an alkaline storage battery that has a crystal structure of an A2B7-type structure as a main phase and is represented by a general formula: (La1-aSma)1-bMgbNicAldCre (where suffixes a, b, c, d, and e meet the following conditions: 0?a?0.35, 0.15?b?0.30, 0.02?d?0.10, 0?e?0.10, 3.20?c+d+e?3.50, and 0<a+e), and an alkaline storage battery using this hydrogen storage alloy for a negative electrode. A vehicle also includes this alkaline storage battery as an electricity supply source for a motor.

Abstract: Provided is a sodium ion conductor whose sodium ion conductivity is improved more than the conventional. The sodium ion conductor is a molecular crystal constituted of NaCB9H10, NaCB11H12, and a sodium halide, the sodium halide having a mol fraction of more than 0 and at most 70 on the basis of the total mol ratio of NaCB9H10, NaCB11H12, and the sodium halide.

Abstract: A cathode active material with high durability and a lithium ion secondary battery. The cathode active material is a cathode active material represented by a general formula Li(1+a)NixCoyMnzWtO2 (?0.05?a?0.2, x=1?y?z?t, 0?y<1, 0?t<1, 0<t?0.03), wherein the cathode active material satisfies the following formula (1): ?1/t1?0.92??(1) where t1 is an element concentration average of insides and grain boundaries of primary particles of a W element, and ?1 is an element concentration standard deviation of the insides and grain boundaries of the primary particles of the W element.

Abstract: A method for manufacturing a solid electrolyte-containing layer that is used in a solid-state battery is disclosed. The method includes forming the solid electrolyte-containing layer by using a slurry containing a boron hydride compound and an alkane compound having 5 or 6 carbon atoms.

Abstract: A sodium ion secondary battery includes a cyclic organic compound as an active material and a complex hydride as a solid electrolyte, wherein the cyclic organic compound has at least two carbonyl groups —C(?O)—, the at least two carbonyl groups are bonded via a single bond or at least one conjugated double bond, and the complex hydride includes a Na cation and a complex ion containing H.

Abstract: To provide an anode material that can improve the efficiency of the initial charging and discharging, the anode material includes an amorphous glassy carbon material that is an anode active material, and a NaMH compound that is a solid electrolyte.

Abstract: A positive electrode active material includes a composite particle. The composite particle includes a core particle and a covering layer. The core particle includes a nickel composite hydroxide. The nickel composite hydroxide is represented by the following formula: Nix1Zn1-x1-y1Coy1(OH)2 (where x1 and y1 satisfy 0.90?x1<1.00, 0?y1?0.01, and 0<(1?x1?y1)). The covering layer covers at least a part of a surface of the core particle. The covering layer includes a cobalt compound. In an X-ray absorption fine structure obtainable through measurement by a total electron yield method with soft X-ray, cobalt L3 absorption edge has a peak top in a range not less than 780.5 eV.

Abstract: Provided is a sodium ion conductor whose sodium ion conductivity is improved more than the conventional. The sodium ion conductor is a molecular crystal constituted of NaCB9H10, NaCB11H12, and a sodium halide, the sodium halide having a mol fraction of more than 0 and at most 70 on the basis of the total mol ratio of NaCB9H10, NaCB11H12, and the sodium halide.

Abstract: A negative electrode active material includes a hydrogen storage alloy. The hydrogen storage alloy has an A2B7 crystal structure. The hydrogen storage alloy includes nickel. The saturation magnetization per unit mass is 1.9 emu·g?1 or more.

Abstract: Provided in the present disclosure is a method for producing a composite cathode active material with low reaction resistance. The method comprises: a coating step of, with a Li ion conductive oxide, coating a cathode active material that is a spinel type oxide including at least a Mn having a valence of +4 to obtain a coated cathode active material; and a heat treating step of heat treating the coated cathode active material to obtain a composite cathode active material; wherein a valence of the Mn in the cathode active material is lower than a valence of the Mn in the cathode active material before coating, and a valence of the Mn is increased by the heat treating.

Abstract: A method of manufacturing an all-solid-state battery includes a lamination step of laminating a deactivated lithium-containing negative electrode active material layer containing deactivated lithium, a solid electrolyte layer for the all-solid-state battery, and a positive electrode active material layer for the all-solid-state battery such that the solid electrolyte layer for the all-solid-state battery is disposed between the deactivated lithium-containing negative electrode active material layer and the positive electrode active material layer for the all-solid-state battery.

Abstract: (a1) A positive electrode active material containing at least one of nickel hydroxide and nickel oxyhydroxide is prepared. (a2) A positive electrode paste is prepared by mixing at least the positive electrode active material, a binder, and a solvent. (a3) A positive electrode for an alkaline secondary battery is manufactured by holding the positive electrode paste on a substrate and drying the positive electrode paste. By using an ion trapping agent in at least one of the positive electrode active material and the positive electrode paste, nitrogen compound ions are reduced.

Abstract: Provided in the present disclosure is a method for producing a composite cathode active material with low reaction resistance. The method comprises: a coating step of, with a Li ion conductive oxide, coating a cathode active material that is a spinel type oxide including at least a Mn having a valence of +4 to obtain a coated cathode active material; and a heat treating step of heat treating the coated cathode active material to obtain a composite cathode active material; wherein a valence of the Mn in the cathode active material is lower than a valence of the Mn in the cathode active material before coating, and a valence of the Mn is increased by the heat treating.

Abstract: A cathode active material with high durability and a lithium ion secondary battery. The cathode active material is a cathode active material represented by a general formula Li(1+a)NixCoyMnzWtO2 (?0.05?a?0.2, x=1?y?z?t, 0?y<1, 0?t<1, 0<t?0.03), wherein the cathode active material satisfies the following formula (1): ?1/t1?0.92??(1) where t1 is an element concentration average of insides and grain boundaries of primary particles of a W element, and ?1 is an element concentration standard deviation of the insides and grain boundaries of the primary particles of the W element.

Abstract: A method of manufacturing an all-solid-state battery includes a lamination step of laminating a deactivated lithium-containing negative electrode active material layer containing deactivated lithium, a solid electrolyte layer for the all-solid-state battery, and a positive electrode active material layer for the all-solid-state battery such that the solid electrolyte layer for the all-solid-state battery is disposed between the deactivated lithium-containing negative electrode active material layer and the positive electrode active material layer for the all-solid-state battery.

Abstract: In a (001) pole figure of the active material particles, where a plane parallel to the substrate is defined as the equatorial plane, a Lotgering factor fa(001) of an A plane and a Lotgering factor fh(001) of a B plane satisfy both Expressions (1) and (2) below, the A plane being an equatorial cross section perpendicular to a line that connects the center of the (001) pole figure and a first point of maximum XRD intensity of peaks attributed to (001) planes at the outer periphery of the equatorial plane, the B plane being an equatorial cross section perpendicular to a line that connects the center of the (001) pole figure and a second point of minimum XRD intensity of peaks attributed to the (001) planes at the outer periphery of the equatorial plane: fa(001)>0.3 ??Expression (1) fa(001)?fb(001)<1.0 ??Expression (2).

Abstract: A manufacturing method for an all-solid-state battery including a positive electrode layer, a negative electrode layer, a solid electrolyte layer, a positive electrode current collector layer, and a negative electrode current collector layer is provided. At least one of the positive and negative electrode layers is an electrode layer containing a sulfide-based solid electrolyte and having a first main surface and a second main surface. The manufacturing method includes: shielding at least a central portion of the first main surface and at least a central portion of the second main surface from an ambient atmosphere; and exposing an outer peripheral portion of the electrode layer to an atmosphere having a dew-point temperature of ?30° C. or higher, with at least the central portion of the first main surface and at least the central portion of the second main surface shielded from the atmosphere.