Chemistry: electrical current producing apparatus – product – and – Current producing cell – elements – subcombinations and... – Electrode
Reexamination Certificate
2000-03-23
2002-05-07
Chaney, Carol (Department: 1745)
Chemistry: electrical current producing apparatus, product, and
Current producing cell, elements, subcombinations and...
Electrode
C429S231100, C429S218100
Reexamination Certificate
active
06383685
ABSTRACT:
BACKGROUND OF THE INVENTION
1. Field of the Invention
The present invention relates generally to a lithium secondary battery provided with a positive electrode, a negative electrode, and a non-aqueous electrolyte, and more particularly, to a lithium secondary battery whose charge/discharge cycle performance is improved upon improvement of a positive electrode active material used for its positive electrode or a negative electrode active material used for its negative electrode.
2. Description of the Related Art
In recent years, secondary batteries have begun to be used in various fields such as electronic equipment and the like. Lithium secondary batteries are attracting great attention as one of new-type batteries having high power and high energy density, and various efforts have been made to develop such lithium secondary batteries.
In order to improve charge/discharge cycle performance of such lithium secondary batteries, one so adapted as to employ as a negative electrode active material a lithium-tungsten composite oxide obtained by mixing tungsten dioxide and a lithium oxide or the like and then calcining the resultant mixture has been proposed, as disclosed in Japanese Patent Laid-Open No. Hei5(1993)-299089.
Unfortunately, however, the above-mentioned lithium-tungsten composite oxide has an unstable crystal structure, as described in the literature (J. J. Auborn and Y. L. Barberio, J. Electorochem. Soc., 134,638 1987). When the lithium-tungsten composite oxide is used as a negative electrode active material in a lithium secondary battery, the lithium-tungsten composite oxide is degraded in capacity of occluding and discharging lithium due to the transformation of its crystal structure. Accordingly, there still exist a problem that the battery cannot attain an adequate improvement in charge/discharge cycle performance.
SUMMARY OF THE INVENTION
An object of the present invention is to improve charge/discharge cycle performance of a lithium secondary battery provided with a positive electrode, a negative electrode, and a non-aqueous electrolyte, upon improvement of a positive electrode active material used for said positive electrode or a negative electrode active material used for said negative electrode.
A lithium secondary battery according to the present invention is a lithium secondary battery provided with a positive electrode, a negative electrode, and a non-aqueous electrolyte, wherein a composite oxide represented by a chemical formula M
X
W
1−X
O
Y
(wherein M denotes at least one type of metal element selected from the group consisting of Cu, V, Cr, Mn, Fe, Co, and Ni; and the conditions of 0<X≦0.46 and 1.5≦Y≦2.5 are satisfied) and having a rutile-type crystal structure or the composite oxide to which lithium is added is used as a positive electrode active material for said positive electrode or a negative electrode active material for said negative electrode.
The literature (Binary Alloy Phase Diagrams, (1986), American Society for Metals: M—O binary phase diagram) shows that the metal element M, which is selected from the group consisting of Cu, V, Cr, Mn, Fe, Co, and Ni, in the composite oxide represented by the foregoing chemical formula forms a stable compound whose decomposition temperature is more than 1000° C. in combination with an oxygen atom O.
When the metal element M is added to tungsten dioxide to obtain a composite oxide represented by the foregoing chemical formula, the composite oxide has a rutile-type crystal structure similar to that of the tungsten dioxide. In addition, the metal elements M are incorporated in some of crystal lattices of the tungsten dioxide to attain a relatively strong chemical bond with oxygen atoms O, thereby stabilizing the crystal structure of the composite oxide.
Accordingly, when the composite oxide represented by the foregoing chemical formula is used as a positive electrode active material or a negative electrode active material in a lithium secondary battery, the composite oxide is prevented from being degraded in capacity of occluding and discharging lithium due to the transformation of its crystal structure. The lithium secondary battery excellent in charge/discharge cycle performance thus can be obtained.
Further, a lithium secondary battery employing a composite oxide represented by a chemical formula M
X
W
1−X
O
Y
(wherein M denotes at least one type of metal element selected from the group consisting of Cu, V, Cr, Mn, Fe, Co, and Ni; and the conditions of 0.02≦X≦0.45 and 1.5≦Y≦2.5 are satisfied) and having a rutile-type crystal structure as a positive electrode active material or a negative electrode active material can attain more excellent charge/discharge cycle performance because the crystal structure of the composite oxide is further stabilized.
When other element such as Cd, La, Ce, Sm, or Mo, which forms highly stable compound in combination with an oxygen atom O as described above, is used as the metal element M in the above-mentioned composite oxide, the resultant composite oxide is still expected to be effective in improving charge/discharge cycle performance of a lithium secondary battery.
When the composite oxide represented by the foregoing chemical formula is used as a positive electrode active material in the lithium secondary battery of the present invention, various materials generally used in lithium secondary batteries may be used as a negative electrode active material. Examples of a usable material include carbon materials capable of electrochemically occluding and discharging Li, such as natural graphite, artificial graphite, coke, and calcined products of organic substances; Li alloys such as an Li—Al alloy, an Li—Mg alloy, an Li—In alloy, and an Li—Al—Mn alloy; and Li metals. However, when the Li alloys or Li metals are used as the negative electrode active material, branch-like dendrite crystals grow during the charging and discharging of the battery so that a short circuit may occur in the battery. Therefore, it is preferable to use the carbon materials as the negative electrode active material.
On the other hand, when the composite oxide represented by the foregoing chemical formula is used as a negative electrode active material in the lithium secondary battery of the present invention, various materials generally used in lithium secondary batteries may be used as a positive electrode active material. When a lithium-containing transition metal oxide such as LiCoO
2
, LiNiO
2
, LiMn
2
O
4
, LiMnO
2
, LiCo
0.5
Ni
0.5
O
2
, LiNi
0.7
Co
0.2
Mn
0.1
O
2
, LiCo
0.9
Ti
0.1
O
2
, or LiCo
0.5
Ni
0.4
Zr
0.1
O
2
is used as the positive electrode active material, the lithium secondary battery with a charge voltage of about 3 V and a discharge voltage of about 2 V is obtained.
Then, a case where the composite oxide represented by the foregoing chemical formula is used as the positive electrode active material and a case where the composite oxide represented by the foregoing chemical formula is used as the negative electrode active material are compared with each other. As a result, it was found that the lithium secondary battery employing the composite oxide as the negative electrode active material requires higher charging voltage, whereby the non-aqueous electrolyte solution is liable to be decomposed. Accordingly, it is preferable to use the composite oxide represented by the forgoing chemical formula as the positive electrode active material.
Further, in the lithium secondary battery according to the present invention, the above-mentioned composite oxide represented by the forgoing chemical formula can be synthesized by calcining each element to compose the composite oxide, a compound containing the element, and the mixture of these.
When they are calcined at temperatures of less than 400° C., the above-mentioned metal element M may not be sufficiently dispersed in crystal lattices of tungsten dioxide. On the other hand, when they are calcined at high temperatures of more than 1500° C., calcined products melt, resulting in uneven composition of the com
Fujimoto Masahisa
Fujitani Shin
Yoshimura Seiji
Chaney Carol
Sanyo Electric Co,. Ltd.
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