Positive active material for nonaqueous electrolyte secondary battery, method of manufacturing the positive active material, electrode for nonaqueous electrolyte secondary battery, nonaqueous electrolyte secondary battery and method of manufacturing the secondary battery

Patent metadata

Field	Value
Publication number	US-9543055-B2
Application number	US-201113997783-A
Country	US
Kind code	B2
Filing date	Dec 27, 2011
Priority date	Dec 27, 2010
Publication date	Jan 10, 2017
Grant date	Jan 10, 2017

Abstract

An object of the present invention is to provide a positive active material for a nonaqueous electrolyte secondary battery which has a large discharge capacity and is superior in charge-discharge cycle performance, initial efficiency and high rate discharge performance, and a nonaqueous electrolyte secondary battery using the positive active material. The present invention pertains to a positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO 2 type, is represented by a compositional formula Li 1+α Me 1−α O 2 (Me is a transition metal element including Co, Ni and Mn, α>0), and has a molar ratio Li/Me of Li to the transition metal element Me of 1.2 to 1.6, wherein a molar ratio Co/Me of Co in the transition metal element Me is 0.02 to 0.23, a molar ratio Mn/Me of Mn in the transition metal element Me is 0.62 to 0.72, and the lithium transition metal composite oxide is observed as a single phase attributed to a space group R3-m on an X-ray diffraction chart when it is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li + ).

First claim

The invention claimed is:

1. A positive active material for a nonaqueous electrolyte secondary battery containing a lithium transition metal composite oxide which has a crystal structure of an α-NaFeO 2 type, is represented by a compositional formula Li 1+α Me 1−α O 2 wherein Me is a transition metal element including Co, Ni and Mn, α>0, and has a molar ratio Li/Me of Li to the transition metal element Me of 1.250 to 1.350, wherein
a molar ratio Co/Me of Co in the transition metal element Me is 0.040 to 0.195,
a molar ratio Mn/Me of Mn in the transition metal element Me is 0.625 to 0.707,
the lithium transition metal composite oxide is observed as a single phase attributed to a space group R3-m on an X-ray diffraction chart when it is electrochemically oxidized up to a potential of 5.0 V (vs. Li/Li + ),
in the lithium transition metal composite oxide, an oxygen position parameter, determined by crystal structure analysis by a Rietveld method at the time of using a space group R3-m as a crystal structure model based on an X-ray diffraction pattern in a state of a discharge end, is 0.260 or less, and
a tapped density of the positive active material is 0.52 to 1.98 g/cm 3 .

2. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein a BET specific surface area is 0.88 m 2 /g or more.

3. The positive active material for a nonaqueous electrolyte secondary battery according to claim 2 , wherein the tapped density is 1.25 to 1.98 g/cm 3 .

4. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein a ratio between the diffraction peak intensity I (003) of (003) line and the diffraction peak intensity I (114) of (114) line based on X-ray diffraction measurement before charge-discharge satisfies I (003) /I (114) ≧1.20.

5. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein oxygen gas is not generated from the lithium transition metal composite oxide when potential is within the range of 4.5 to 4.6 V (vs. Li/Li + ) as a potential of a positive electrode.

6. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein when the positive active material is used in a battery as a material of a positive electrode and the battery is charged so that a potential of the positive electrode is within the range of 4.5 to 4.6 V (vs. Li/Li + ), a volume ratio of oxygen gas generated from the lithium transition metal composite oxide to the total amount of nitrogen gas and the oxygen gas contained in the battery is 0.20 to 0.25.

7. The positive active material for a nonaqueous electrolyte secondary battery according to claim 5 , wherein oxygen gas is not generated from the lithium transition metal composite oxide when potential is within the range of 4.55 to 4.6 V (vs. Li/Li + ) as a potential of a positive electrode.

8. The positive active material for a nonaqueous electrolyte secondary battery according to claim 5 , wherein the charge is a charge in the initial charge-discharge.

9. The positive active material for a nonaqueous electrolyte secondary battery according to claim 5 , wherein the positive active material has a plateau potential in a charge range, and any potential within the range of 4.5 to 4.6 V (vs. Li/Li + ) is the plateau potential or more.

10. The positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , wherein the lithium transition metal composite oxide is obtained by mixing/sintering a coprecipitated precursor of compounds of the transition metal elements including Co, Ni and Mn, and a lithium compound.

11. A method of manufacturing the positive active material for a nonaqueous electrolyte secondary battery according to claim 1 , comprising the steps of coprecipitating compounds of transition metal elements including Co, Ni and Mn in a solution to produce a coprecipitated precursor; and mixing/sintering the coprecipitated precursor and a lithium compound.

12. The method of manufacturing a positive active material for a nonaqueous electrolyte secondary battery according to claim 11 , wherein a pH in the step of coprecipitating compounds of transition metal elements including Co, Ni and Mn in a solution to produce a coprecipitated precursor is 8.5 to 11.0.

13. The method of manufacturing a positive active material for a nonaqueous electrolyte secondary battery according to claim 11 , wherein a sintering temperature in the step of mixing/sintering the coprecipitated precursor and a lithium compound is 800 to 940° C.

14. An electrode for a nonaqueous electrolyte secondary battery containing the positive active material for a nonaqueous electrolyte secondary battery according to claim 1 .

15. A nonaqueous electrolyte secondary battery including the electrode for a nonaqueous electrolyte secondary battery according to claim 14 .

16. The nonaqueous electrolyte secondary battery according to claim 15 , wherein a charge method, in which a maximum achieved potential of a positive electrode at the time of charge is lower than 4.4 V (vs. Li/Li + ), is employed at the time of use.

Assignees

• Endo Daisuke
• Katayama Yoshihiro
• Murai Tetsuya
• Shibata Masafumi
• Gs Yuasa Int Ltd

Inventors

• Endo Daisuke
• Katayama Yoshihiro
• Murai Tetsuya
• Shibata Masafumi

Classifications

• C01P2004/61

  Micrometer sized, i.e. from 1-100 micrometer · CPC title

• H01M4/0471

  involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis · CPC title

• C01P2006/11

  Powder tap density · CPC title

• C01G45/1221

  Manganates or manganites with trivalent manganese, tetravalent manganese or mixtures thereof · CPC title

• H01B1/08 Primary

  oxides · CPC title