Abstract: In a non-aqueous electrolyte secondary battery comprising: a negative electrode containing, as a negative electrode active material, at least a material capable of absorbing and desorbing lithium ions or metal lithium; a positive electrode; and an electrolyte, an oxide containing nickel and manganese elements, the material comprising primary particles of the oxide having a twining portion and a superlattice arrangement of a [3×3] R30° when assigned as R3-m is used as a positive electrode active material.

Abstract: A non-aqueous electrolyte secondary battery including a unit cell including a positive electrode, a negative electrode, a separator disposed between the positive electrode and the negative electrode, and a non-aqueous electrolyte, the positive electrode capacity being greater than the negative electrode capacity, and at least a portion of the non-aqueous electrolyte is gasified during charging.

Abstract: The present invention relates to a positive electrode active material comprising a lithium-containing composite oxide containing nickel with an oxidation state of 2.0 to 2.5 and manganese with an oxidation state of 3.5 to 4.0, the oxidation state determined by the shifts of energy at which absorption maximum is observed in the X-ray absorption near-K-edge structures, and to a non-aqueous electrolyte secondary battery using the same, the positive electrode active material being characterized in having a high capacity, a long storage life and excellent cycle life.

Abstract: A positive electrode active material for a non-aqueous electrolyte battery comprising a lithium-containing transition metal oxide, produced with the use of a dry precursor obtained by: introducing an alkaline solution together with an aqueous solution containing two or more of transition metal salts or two kinds or more of aqueous solutions of different transition metal salts into a reaction vessel to obtain a hydroxide or an oxide as a precursor through coprecipitation with a reductant being coexistent or an inert gas being supplied; and drying the precursor at 300 to 500° C. to obtain a dry precursor.

Abstract: In order to provide a 3V level non-aqueous electrolyte secondary battery with a flat voltage and excellent cycle life at a high rate with low cost, the present invention provides a positive electrode represented by the formula: Li2±?[Me]4O8?x, wherein 0??<0.4, 0?x<2, and Me is a transition metal containing Mn and at least one selected from the group consisting of Ni, Cr, Fe, Co and Cu, said active material exhibiting topotactic two-phase reactions during charge and discharge.

Abstract: As an alternative technique to lead-acid batteries, the present invention provides an inexpensive 2 V non-aqueous electrolyte secondary battery having excellent cycle life at a high rate by preventing volume change during charge and discharge. The non-aqueous electrolyte secondary battery uses: a positive electrode active material having a layered structure, being represented by chemical formula Li1±?[Me]O2, where 0??<0.2, and Me is a transition metal including Ni and at least one selected from the group consisting of Mn, Fe, Co, Ti and Cu, and including elemental nickel and elemental cobalt in substantially the same ratio; and a negative electrode active material including Li4Ti5O12 (Li1/3Ti5/3]O4).

Abstract: In order to provide a 3V level non-aqueous electrolyte secondary battery with a flat voltage and excellent cycle life at a high rate with low cost, the present invention provides a positive electrode represented by the formula: Li2±?[Me]4O8?x, wherein 0??<0.4, 0?x<2, and Me is a transition metal containing Mn and at least one selected from the group consisting of Ni, Cr, Fe, Co and Cu, said active material exhibiting topotactic two-phase reactions during charge and discharge.

Abstract: As an alternative technique to lead-acid batteries, the present invention provides an inexpensive 2 V non-aqueous electrolyte secondary battery having excellent cycle life at a high rate by preventing volume change during charge and discharge. The non-aqueous electrolyte secondary battery uses: a positive electrode active material having a layered structure, being represented by chemical formula Li1±?[Me]O2, where 0??<0.2, and Me is a transition metal including Ni and at least one selected from the group consisting of Mn, Fe, Co, Ti and Cu, and including elemental nickel and elemental cobalt in substantially the same ratio; and a negative electrode active material including Li4Ti5O12(Li[Li1/3Ti5/3]O4).

Abstract: A nonaqueous electrolytic secondary cell produced at low cost and having a large capacity comprises a negative electrode having an active material mainly composed of a material that at least absorbs and releases lithium ions or metallic lithium, a positive electrode, and an electrolyte. The active material of the positive electrode is an oxide containing nickel, manganese, and cobalt, and the contents of the elements are substantial the same.

Abstract: In a non-aqueous electrolyte secondary battery comprising: a negative electrode containing, as a negative electrode active material, at least a material capable of absorbing and desorbing lithium ions or metal lithium; a positive electrode; and an electrolyte, an oxide containing nickel and manganese elements, the material comprising primary particles of the oxide having a twining portion and a superlattice arrangement of a [{square root}{square root over ( )}3×{square root}{square root over ( )}3] R30° when assigned as R3-m is used as a positive electrode active material.

Abstract: To provide a non-aqueous electrolyte secondary battery in which the amount of Li deposited is small and the battery surface temperature does not increase so much, a positive electrode active material comprising crystal particles of an oxide having a layered single-phase crystal structure and a composition represented by the formula (1): LiNi2/3Mn1/3O2, wherein the arrangement of oxygen atoms constituting the oxide is a cubic close-packed structure is used.

Abstract: The present invention provides a high-capacity and low-cost non-aqueous electrolyte secondary battery, comprising: a negative electrode containing, as a negative electrode active material, a ssubstance capable of absorbing/desorbing lithium ions and/or metal lithium; a separator; a positive electrode; and an electrolyte, wherein the positive electrode active material contained in the positive electrode is composed of crystalline particles of an oxide containing two kinds of transition metal elements, the crystalline particles having a layered crystal structure, and oxygen atoms constituting the oxide forming a cubic closest packing structure.

Abstract: The present invention relates to a positive electrode active material comprising a lithium-containing composite oxide containing nickel with an oxidation state of 2.0 to 2.5 and manganese with an oxidation state of 3.5 to 4.0, the oxidation state determined by the shifts of energy at which absorption maximum is observed in the X-ray absorption near-K-edge structures, and to a non-aqueous electrolyte secondary battery using the same, the positive electrode active material being characterized in having a high capacity, a long storage life and excellent cycle life.

Abstract: The present invention discloses a non-aqueous electrolyte secondary battery comprising: a negative electrode containing metallic lithium or a substance at least capable of absorbing/desorbing lithium ion; a separator; a positive electrode; and an electrolyte, wherein the active material for the positive electrode comprises an oxide containing nickel element and manganese element in substantially the same atomic ratios. The non-aqueous electrolyte secondary battery thus fabricated is low cost in construction and has a high capacity.

Abstract: A positive electrode active material for a non-aqueous electrolyte battery comprising a lithium-containing transition metal oxide, produced with the use of a dry precursor obtained by: introducing an alkaline solution together with an aqueous solution containing two or more of transition metal salts or two kinds or more of aqueous solutions of different transition metal salts into a reaction vessel to obtain a hydroxide or an oxide as a precursor through coprecipitation with a reductant being coexistent or an inert gas being supplied; and drying the precursor at 300 to 500° C. to obtain a dry precursor.