Patent classifications
C01G53/00
Positive-electrode material for lithium ion secondary battery, method for producing the same, and lithium ion secondary battery
A positive-electrode material for a lithium ion secondary battery contains a lithium complex compound that is represented by the formula: Li.sub.1+aNi.sub.bMn.sub.cCo.sub.dTi.sub.eM.sub.fO.sub.2+α, and has an atomic ratio Ti.sup.3+/Ti.sup.4+ between Ti.sup.3+ and Ti.sup.4+, as determined through X-ray photoelectron spectroscopy, of greater than or equal to 1.5 and less than or equal to 20. In the formula, M is at least one element selected from the group consisting of Mg, Al, Zr, Mo, and Nb, and a, b, c, d, e, f, and a are numbers satisfying −0.1≤a≤0.2, 0.7<b≤0.9, 0≤c<0.3, 0≤d<0.3, 0<e≤0.25, 0≤f<0.3, b+c+d+e+f=1, and −0.2≤α≤0.2.
Positive-electrode material for lithium ion secondary battery, method for producing the same, and lithium ion secondary battery
A positive-electrode material for a lithium ion secondary battery contains a lithium complex compound that is represented by the formula: Li.sub.1+aNi.sub.bMn.sub.cCo.sub.dTi.sub.eM.sub.fO.sub.2+α, and has an atomic ratio Ti.sup.3+/Ti.sup.4+ between Ti.sup.3+ and Ti.sup.4+, as determined through X-ray photoelectron spectroscopy, of greater than or equal to 1.5 and less than or equal to 20. In the formula, M is at least one element selected from the group consisting of Mg, Al, Zr, Mo, and Nb, and a, b, c, d, e, f, and a are numbers satisfying −0.1≤a≤0.2, 0.7<b≤0.9, 0≤c<0.3, 0≤d<0.3, 0<e≤0.25, 0≤f<0.3, b+c+d+e+f=1, and −0.2≤α≤0.2.
Transition metal precursor having low tap density and lithium transition metal oxide having high particle strength
Disclosed are a transition metal precursor for preparation of a lithium transition metal oxide, in which a ratio of tap density of the precursor to average particle diameter D50 of the precursor satisfies the condition represented by Equation 1 below, and a lithium transition metal oxide prepared using the same.
Positive electrode active material for secondary battery, and secondary battery comprising the same
In one embodiment, a positive electrode active material for a secondary battery, the positive electrode active material being a primary particle having a monolithic structure that includes a lithium composite metal oxide of Formula 1 below, wherein the primary particle has an average particle size (D.sub.50) of 2 μm to 20 μm and a Brunauer-Emmett-Teller (BET) specific surface area of 0.15 m.sup.2/g to 0.5 m.sup.2/g, and wherein the positive electrode active material has a rolling density of 3.0 g/cc or higher under a pressure of 2 ton.Math.f:
Li.sub.aNi.sub.1-x-yCo.sub.xM1.sub.yM3.sub.zM2.sub.wO.sub.2 [Formula 1] in Formula 1, M1 is at least one selected from the group consisting of Al and Mn, M2 is any one or two or more elements selected from the group consisting of Zr, Ti, Mg, Ta, and Nb, M3 is any one or two or more elements selected from the group consisting of W, Mo, and Cr, and 1.0≤a≤1.5, 0≤x≤0.5, 0≤y≤0.5, 0.005≤z≤0.01, 0≤w≤0.04, 0<x+y≤0.7.
COBALT-FREE POSITIVE ELECTRODE MATERIAL FOR LITHIUM ION BATTERY, PREPARATION METHOD THEREFOR, AND LITHIUM ION BATTERY
Provided are a cobalt-free positive electrode material for a lithium ion battery, a preparation method therefor and a lithium ion battery. The method for preparing the cobalt-free positive electrode material for the lithium ion battery comprises: mixing lithium nickel manganese oxide with sulfate, so as to obtain a first mixture; and reacting the first mixture at a predetermined temperature, so as to obtain the cobalt-free positive electrode material. The cobalt-free positive electrode material comprises lithium nickel manganese oxide and a cladding layer of an outer surface thereof, and the cladding layer comprises lithium sulphate. The lithium ion battery comprises the cobalt-free positive electrode material. The cobalt-free positive electrode material has a relatively high electrical performance and a relatively low alkali content.
CATHODE ACTIVE MATERIAL, METHOD FOR MANUFACTURING THE SAME, AND SECONDARY LITHIUM ION BATTERY INCLUDING THE SAME
Embodiments of the present invention relate to a cathode active material, a method for manufacturing the same, and a lithium secondary battery including the same.
According to an embodiment, a cathode active material can be provided, the cathode active material comprising: a lithium metal oxide including a core and a shell disposed on a surface of the core; and a coating layer disposed on a surface of the lithium metal oxide, wherein a c value that satisfies Equation 1 and is in a range of 0.3 to 0.7, and the core and the shell have a layered crystalline structure.
c=b/a [Equation 1]
(in Equation 1, a is a peak at 530 to 533 eV and b is a peak at 528 to 531 eV in an XPS spectrum of the coating layer)
Positive Electrode Active Material Layer, Active Material Layer, Positive Electrode, Secondary Battery, and Vehicle
A secondary battery with favorable cycle performance is provided. Alternatively, a secondary battery with higher capacity is provided. A positive electrode active material layer including a first graphene layer, a second graphene layer, and a positive electrode active material. The first graphene layer includes a first region covering the positive electrode active material. The second graphene layer includes a second region covering the positive electrode active material and a third region overlapping with the first region. The first region includes a plane positioned between the positive electrode active material and the third region and formed of arranged six-membered carbon rings. The positive electrode active material includes a fourth region with a layered rock-salt structure. A lithium layer with a layered rock-salt structure included in the fourth region is substantially perpendicular to the plane formed of six-membered carbon rings and included in the second region.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY, AND NON-AQUEOUS ELECTROLYTE SECONDARY BATTERY
This positive electrode active material for a non-aqueous electrolyte secondary battery contains a lithium-transition metal composite compound. The lithium-transition metal composite compound is represented by general formula Li.sub.xMn.sub.yNi.sub.zMe.sub.αO.sub.aF.sub.b (in the formula, 1≤x≤1.2, 0.4≤y≤0.8; 0≤z≤0.4, x+y+z=2, 0<α<0.05, 1.8≤a≤2, and 1.8≤a±b≤2.2 are satisfied, and Me represents at least two kinds of elements selected from metal elements other than Li, Mn, and Ni) and Me includes at least one kind of element having an ion radius of 0.6 Å or more.
POSITIVE ELECTRODE ACTIVE MATERIAL FOR ALL-SOLID-STATE LITHIUM ION SECONDARY BATTERY, METHOD FOR PRODUCING THE SAME, AND ALL-SOLID-STATE LITHIUM ION SECONDARY BATTERY
A positive electrode active material for an all-solid-state lithium ion secondary battery, containing: a lithium-metal composite oxide particle having a niobium solid solution layer and a center other than the niobium solid solution layer; and a coating layer coating at least a part of a surface of the lithium-metal composite oxide particle and formed of a compound containing lithium and niobium, an average thickness of the coating layer is 2 nm or more and 1 μm or less, and an average thickness of the niobium solid solution layer is 0.5 nm or more and 20 nm or less.
METHOD FOR REUSING ACTIVE MATERIAL BY USING POSITIVE ELECTRODE SCRAP
There is provided a method for collecting and reusing an active material from positive electrode scrap. The method for reusing a positive electrode active material of the present disclosure includes (a) thermally treating positive electrode scrap comprising an active material layer on a current collector in air for thermal decomposition of a binder and a conductive material in the active material layer, to separate the current collector from the active material layer, and collecting an active material in the active material layer, (b-1) washing the active material collected from the step (a) with a lithium compound solution which is basic in an aqueous solution, (b-2) mixing the active material washed from the step (b-1) with a lithium precursor aqueous solution and spray drying, and (c) annealing the active material spray dried from the step (b-2) to obtain a reusable active material.