Titanium oxide-based compound for electrode and lithium secondary battery using the same
The present invention provides a novel titanium-based composite oxide being usable as an electrode material for a lithium secondary battery and having a high capacity and an excellent cycle stability, a method for producing the same and a lithium secondary battery using the titanium-based composite oxide. Disclosed is a compound obtained by compositing titanium oxide with elements other than titanium, specifically a titanium-based composite oxide wherein the relevant chemical formula is Ti (1-x) M x O y , M is the element Nb or the element P, or a combination of these two elements in an optional ratio therebetween, x is such that 0<x<0.17, y is such that 1.8≦y≦2.1, x is the sum of Nb and P when M is a combination of the element Nb and the element P, and the present invention provides a lithium secondary battery using as an electrode the titanium-based composite oxide.
1. A titanium-based composite oxide represented by the chemical formula of Ti (1-x) M x O y ,
wherein M is elemental Nb or elemental P, or a combination of these two elements in an optional ratio therebetween, x is represented as 0<x<0.17, y is represented as 2.0≦y≦2.1, in the proviso that when M is a combination of elemental Nb and elemental P, x is the sum of the molar proportions of Nb and P, and
wherein the crystal structure of the titanium-based composite oxide comprises a tunnel structure or a layered structure, is monoclinic, belongs to a space group C2/m, and has a diffraction pattern based on the powder X-ray diffraction corresponding to the bronze structure.
2. The titanium-based composite oxide according to claim 1 , wherein the specific surface area is in a range from 5 m 2 /g to 50 m 2 /g.
3. An electrode for use in a battery,
the electrode using as the electrode active material a titanium-based composite oxide represented by the chemical formula of Ti (1-x) M x O y ,
wherein M is elemental Nb or elemental P, or a combination of these two elements in an optional ratio therebetween, x is represented as 0<x<0.17, y is represented as 2.0≦y≦2.1, in the proviso that when M is a combination of elemental Nb and elemental P, x is the sum of the molar proportions of Nb and P, and
wherein the crystal structure of the titanium-based composite oxide comprises a tunnel structure or a layered structure, is monoclinic, belongs to a space group C2/m, and has a diffraction pattern based on the powder X-ray diffraction corresponding to the bronze structure.
4. The electrode for use in a battery according to claim 3 , wherein the specific surface area of the titanium-based composite oxide is in a range from 5 m 2 /g to 50 m 2 /g.
5. A lithium secondary battery comprising
an electrode using as the electrode active material a titanium-based composite oxide represented by the chemical formula of Ti (1-x) M x O y ,
wherein M is elemental Nb or elemental P, or a combination of these two elements in an optional ratio therebetween, x is represented as 0<x<0.17, y is represented as 2.0≦y≦2.1, in the proviso that when M is a combination of elemental Nb and elemental P, x is the sum of the molar proportions of Nb and P, and
wherein the crystal structure of the titanium-based composite oxide comprises a tunnel structure or a layered structure, is monoclinic, belongs to a space group C2/m, and has a diffraction pattern based on the powder X-ray diffraction corresponding to the bronze structure.
6. The lithium secondary battery according to claim 5 , wherein the specific surface area of the titanium-based composite oxide is in a range from 5 m 2 /g to 50 m 2 /g.
7. The coin lithium secondary battery according to claim 5 , wherein when Li metal is used as a counter electrode which is for the negative electrode, at 35 mA per 1 g of the positive electrode active material, the initial discharge capacity that is Li intercalation capacity is 210 mAh/g or more, the discharge capacity that is Li intercalation capacity at the third cycle is 195 mAh/g or more, and the retention rate of the discharge capacity at the 50th cycle relative to the discharge capacity at the third cycle is 95% or more.