US2014212749A1PendingUtilityA1
Method for Preparing Positive Electrode Active Material for Lithium Secondary Battery, Positive Electrode Active Material for Lithium Secondary Battery, and Lithium Secondary Battery Including Same
Est. expiryMar 13, 2032(~5.6 yrs left)· nominal 20-yr term from priority
H01M 4/505H01M 10/052H01M 4/525H01M 4/1391Y02E60/50C01G 53/50Y02E60/10Y02P70/50C01P 2004/80C01P 2004/61C01P 2002/52H01M 4/131C01P 2004/84C01P 2006/40C01D 15/02H01M 8/04H01M 2004/028H01M 4/5825H01M 4/0471H01M 10/0525H01M 4/485
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Abstract
Disclosed are a method for preparing a positive electrode active material for a lithium secondary battery and a positive electrode active material for a lithium secondary battery, the method including: preparing a mixture of a precursor represented by Chemical Formula 1 below, a lithium composite oxide represented by Chemical Formula 2 below and capable of intercalating/deintercalating lithium ions, and a lithium feed material; and firing the prepared mixture: A(OH) 2-a [Chemical Formula 1] Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 2]
Claims
exact text as granted — not AI-modifiedWhat is claimed is:
1 . A method for preparing a positive electrode active material for a lithium secondary battery, the method comprising:
preparing a mixture of a precursor represented by Chemical Formula 1 below, a lithium composite oxide represented by Chemical Formula 2 below and capable of intercalating/deintercalating lithium ions, and a lithium feed material; and firing the prepared mixture:
A(OH) 2-a [Chemical Formula 1]
wherein in Chemical Formula 1, A=Ni α Co β Mn γ ; and −0.3≦a≦0.3, 0.5≦α≦0.64, 0.15≦β≦0.29, and 0.21≦γ≦0.35,
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 2]
wherein in Chemical Formula 2, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.35≦α<0.5, 0.19≦β≦0.34, and 0.31≦γ≦0.46.
2 . The method of claim 1 , wherein the weight ratio of the precursor represented by Chemical Formula 1 to the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions is 95/5 to 70/30.
3 . The method of claim 1 , wherein the precursor represented by Chemical Formula 1 has a particle diameter of 8 to 12 μm.
4 . The method of claim 1 , wherein the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions has a particle diameter of 3 to 8 μm.
5 . The method of claim 1 , wherein the lithium feed material is nitrate, carbonate, acetate, oxalate, oxide, hydroxide, or sulfate, which contains lithium, or a combination thereof.
6 . The method of claim 1 , wherein the precursor represented by Chemical Formula 1 is represented by Chemical Formula 3 below:
A(OH) 2-a [Chemical Formula 3]
wherein in Chemical Formula 3, A=Ni α Co β Mn γ ; and −0.3≦a≦0.3, 0.5≦α≦0.61, 0.15≦β≦0.26, and 0.24≦γ≦0.35.
7 . The method of claim 1 , wherein the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions is represented by Chemical Formula 4 below:
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 4]
wherein in Chemical Formula 4, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.43≦α<0.5, 0.19≦β≦0.26, and 0.31≦γ≦0.38.
8 . The method of claim 1 , wherein in the firing of the prepared mixture, the firing temperature is 800 to 1000° C.
9 . The method of claim 1 , wherein the particle diameter of the precursor represented by Chemical Formula 1 is larger than the particle diameter of the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions.
10 . The method of claim 1 , wherein the amount of remaining water-soluble lithium after the firing of the prepared mixture is reduced to 20 to 50% based on the amount of remaining water-soluble lithium when the precursor represented by Chemical Formula 1 is fired alone.
11 . The method of claim 1 , wherein in the positive electrode active material for a lithium secondary battery, which is obtained by performing the firing of the prepared mixture, the surface Ni content of a positive electrode active material derived from Chemical Formula 1 is further reduced than the surface Ni content of a positive electrode active material prepared by firing the precursor represented by Chemical Formula 1 alone.
12 . The method of claim 11 , wherein the surface Ni content of the positive electrode active material derived from Chemical Formula 1 is further reduced by less than 5% than the surface Ni content of the positive electrode active material prepared by firing the precursor represented by Chemical Formula 1 alone.
13 . The method of claim 11 , wherein, when ten particles of the positive electrode active material derived from Chemical Formula 1 are randomly selected from the positive electrode active material for a lithium secondary battery and surfaces thereof are analyzed, the standard deviation of the Ni content is smaller than 1.00.
14 . A positive electrode active material for a lithium secondary battery, the positive electrode active material comprising: a lithium composite oxide represented by Chemical Formula 5 below and capable of intercalating/deintercalating lithium ions; and a lithium composite oxide represented by Chemical Formula 2 below and capable of intercalating/deintercalating lithium ions,
wherein the lithium composite oxide represented by Chemical Formula 5 below and capable of intercalating/deintercalating lithium ions is prepared from a precursor, and wherein the surface Ni content of the lithium composite oxide represented by Chemical Formula 5 below and capable of intercalating/deintercalating lithium ions is further reduced than the surface Ni content of a lithium composite oxide prepared by firing the precursor alone:
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 5]
wherein in Chemical Formula 5, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.5≦α<0.64, 0.15≦β≦0.29, and 0.21≦γ≦0.35, and
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 2]
wherein in Chemical Formula 2, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.35≦α<0.5, 0.19≦β≦0.34, and 0.31≦γ≦0.46.
15 . The positive electrode active material of claim 14 , wherein the particle diameter of the lithium composite oxide represented by Chemical Formula 5 and capable of intercalating/deintercalating lithium ions is larger than the particle diameter of the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions.
16 . The positive electrode active material of claim 14 , wherein the lithium composite oxide expressed by Chemical Formula 5 and capable of intercalating/deintercalating lithium ions has a particle diameter of 8 to 12 μm.
17 . The positive electrode active material of claim 14 , wherein the lithium composite oxide expressed by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions has a particle diameter of 3 to 8 μm.
18 . The positive electrode active material of claim 14 , wherein the weight ratio of the lithium composite oxide represented by Chemical Formula 5 and capable of intercalating/deintercalating lithium ions to the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions is 95/5 to 70/30.
19 . The positive electrode active material of claim 14 , wherein the lithium composite oxide represented by Chemical Formula 5 and capable of intercalating/deintercalating lithium ions is represented by Chemical Formula 6 below:
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 6]
wherein in Chemical Formula 6, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.50≦α<0.61, 0.15≦β≦0.26, and 0.24≦γ≦0.35.
20 . The positive electrode active material of claim 14 , wherein the lithium composite oxide represented by Chemical Formula 2 and capable of intercalating/deintercalating lithium ions is represented by Chemical Formula 4 below:
Li[Li z A (1-z-a) D a ]E b O 2-b [Chemical Formula 4]
wherein in Chemical Formula 4, A=Ni α Co β Mn γ ; D is at least one element selected from the group consisting of Mg, Al, B, Zr, and Ti; E is at least one element selected from the group consisting of P, F, and S; and −0.05≦z≦0.1, 0≦a≦0.05, 0≦b≦0.05, 0.43≦α<0.5, 0.19≦β≦0.26, and 0.31≦γ≦0.38.
21 . A lithium secondary battery comprising a positive electrode, an anode, and an electrolyte,
wherein the positive electrode includes a current collector and a positive electrode active material layer formed on the current collector, and wherein the positive electrode active material layer contains the positive electrode active material of claim 14 .Join the waitlist — get patent alerts
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