Lithium secondary batteries for improving life span and resistance properties are disclosed. In an aspect, a cathode composition for a lithium secondary battery includes a cathode active material that includes a first cathode active material particle having a secondary particle shape and a second cathode active material particle having a single particle shape, and a conductive material including a linear-type conductive material.

An organic electrolytic solution includes a first lithium salt; an organic solvent; a bicyclic sulfate-based compound represented by Formula 1 below; and a monocyclic phosphate-based compound represented by Formula K1 below:

##STR00001## wherein in Formula 1, each of A.sub.1, A.sub.2, A.sub.3, and A.sub.4 is independently a covalent bond, a substituted or unsubstituted C.sub.1-C.sub.5 alkylene group, a carbonyl group, or a sulfinyl group, wherein both A.sub.1 and A.sub.2 are not a covalent bond and both A.sub.3 and A.sub.4 are not a covalent bond, and in Formula K1, each of A.sub.5 and A.sub.6 is independently a substituted or unsubstituted C.sub.1-C.sub.5 alkylene group.

A positive electrode active material for lithium secondary batteries includes a lithium composite metal compound containing secondary particles that are aggregates of primary particles which are capable of being doped or dedoped with lithium ions and satisfies all of specific requirements (1) to (4).

A method for producing a lithium-transition metal composite oxide includes steps of preparing a first mixture including a lithium-containing compound and a transition metal compound, obtaining a compressed body by compressing the first mixture at least once, obtaining a molded body by molding at least the compressed body, and obtaining a sintered body by sintering the molded body.

This disclosure provides systems, methods, and apparatus related to lithium-ion batteries. In one aspect, a method includes synthesizing an intermediate selected from a group of a nickel-manganese-cobalt nitrate, a nickel-manganese-cobalt acetate, a nickel-manganese-cobalt sulfate, a nickel-manganese-cobalt chloride, and a nickel-manganese-cobalt phosphate. The intermediate is mixed with a lithium salt selected from a group of LiOH, LiCl, LiNO.sub.3, LiSO.sub.4, LiF, LiBr, Li.sub.3PO.sub.4, Li.sub.2CO.sub.3, and combinations thereof to form a mixture. The mixture is annealed at a sequence of temperatures and times to form a plurality of single crystals of a lithium nickel-manganese-cobalt oxide, with no cooling of the mixture between operations of the sequence of temperatures and times.

This application provides a positive active material and a preparation method thereof, an electrochemical battery, a battery module, a battery pack, and an apparatus. The positive active material includes an inner core and a coating layer, where the coating layer coats a surface of the inner core. The inner core is selected from a ternary material with a molecular formula of Li.sub.1+a[Ni.sub.xCo.sub.yMn.sub.zM.sub.bM′.sub.c]O.sub.2−dY.sub.d, where distribution of each of the doping elements M, M′, and Y in the inner core meets the following condition: there is a reduced mass concentration gradient from an outer side of the inner core to a center of the inner core. The positive active material herein features high gram capacity, high structural stability, and high thermal stability, so that the electrochemical battery has excellent cycle performance and storage performance and high initial discharge gram capacity.

The present disclosure discloses a lithium-manganese rich material and a preparation method and a use thereof.

The present disclosure provides a cobalt-free cathode material of a lithium ion battery, a method for preparing the cobalt-free cathode material, and the lithium ion battery. A general formula of the cobalt-free cathode material is Li.sub.xNi.sub.aMn.sub.bR.sub.cO.sub.2, wherein, 1≤x≤1.15, 0.5≤a≤0.95, 0.02≤b≤0.48, 0<c≤0.05, and R is aluminum or tungsten. Therefore, as the cobalt-free cathode material is free of metal cobalt, the cost of the cathode material can be lowered effectively. Aluminum or tungsten in the cobalt-free cathode material can stabilize a crystal structure of the cathode material better, such that the lithium ion battery has excellent rate capability and cycle performance, and furthermore, good cycling stability of the lithium ion battery can be still maintained under a high-temperature and high-pressure testing condition.

The present exemplary embodiments relate to a cathode active material, a manufacturing method thereof, and a lithium secondary battery including the same. A cathode active material according to an exemplary embodiment is a lithium metal oxide particle in the form of a secondary particle including a primary particle, a coating layer including a boron compound is positioned on at least a portion of a surface of the primary particle, and the boron compound includes an amorphous structure.

A lithium battery positive active material precursor, a preparation method therefor and the use thereof are provided. The precursor has a chemical formula of Ni.sub.xCo.sub.yM.sub.z(OH).sub.2, wherein M is at least one metal selected from the group consisting of Fe, Cr, Cu, Ti, Mg, W, Mo, Nb, Zn, Sn, Zr, Ga, Mn and Al, 0.3≤x≤1, 0<y≤0.5, 0<z≤0.3; and the precursor comprises aggregates of platy monocrystals and polyhedral monocrystal particles. In the XRD pattern of the precursor, I(001), I(100) and I(101) satisfy the following relationship: I(001)/I(100) is not less than about 1.5, and I(001)/I(101) is not less than about 1.2.