Abstract: A method for preparing a positive electrode active material for a secondary battery is provided. The method includes preparing a lithium composite transition metal oxide including nickel, cobalt, and manganese (Mn), wherein the content of the nickel in the total content of the transition metal is 60 mol % or greater. The lithium composite transition metal oxide, MgF2 as a fluorine (F) coating source, and a boron (B) coating source undergoes dry mixing and heat treatment to form a coating portion on the particle surface of the lithium composite transition metal oxide. In addition, a positive electrode active material prepared as described above, is also provided.

Abstract: The present invention relates to a method of preparing a positive electrode active material precursor for a lithium secondary battery in which particle size uniformity and productivity may be improved by using three reactors, a method of preparing a positive electrode active material for a lithium secondary battery by using the above-prepared positive electrode active material precursor for a lithium secondary battery, and a positive electrode for a lithium secondary battery and a lithium secondary battery which include the above-prepared positive electrode active material for a lithium secondary battery.

Abstract: The present invention relates to a method of preparing a positive electrode active material precursor for a lithium secondary battery in which particle size uniformity and productivity may be improved by using three reactors, a method of preparing a positive electrode active material for a lithium secondary battery by using the above-prepared positive electrode active material precursor for a lithium secondary battery, and a positive electrode for a lithium secondary battery and a lithium secondary battery which include the above-prepared positive electrode active material for a lithium secondary battery.

Abstract: A method for preparing a positive electrode active material is provided. The method includes a first step for adding, to a reactor, a reaction solution including a transition metal-containing solution containing at least one among nickel, cobalt, and manganese, an ammonium ion-containing solution, and a basic aqueous solution to form seeds of precursor particles; a second step for preparing carbon-introduced precursor particles by adding a carbon source to the reactor when the precursor particles grow until the average particle diameter (D50) is 30% in size of the average particle diameter (D50) of the finally prepared precursor particles; and a third step for mixing the carbon-introduced precursor particles and a lithium raw material and sintering the mixture at a temperature of 750° C. to 950° C. to prepare positive electrode active material particles.

Abstract: A method for preparing a positive electrode active material for a secondary battery is provided. The method includes preparing a lithium composite transition metal oxide including nickel, cobalt, and manganese, wherein the content of the nickel in the total content of the transition metal is 60 mol % or greater. The lithium composite transition metal oxide, MgF2 as a fluorine (F) coating source, and a boron (B) coating source undergoes dry mixing and heat treatment to form a coating portion on the particle surface of the lithium composite transition metal oxide. In addition, a positive electrode active material prepared as described above, is also provided.

Abstract: A positive electrode active material for a lithium secondary battery includes a lithium composite transition metal oxide including transition metals including nickel (Ni), cobalt (Co), and manganese (Mn), and the lithium composite transition metal oxide is doped with doping elements including cobalt (Co) and titanium (Ti). The lithium composite transition metal oxide includes at least one lithium layer and at least one transition metal layer including the transition metals, and the lithium layer and the transition metal layer are alternately arranged. The thickness of the lithium layer ranges from 2.146 ? to 2.182 ?, and the thickness of the transition metal layer ranges from 2.561 ? to 2.595 ?A.