IP Library › Granted Patent US 9,231,251
Granted Patent B2
US 9,231,251 · App. 13/852,468 · Granted Jan 5, 2016

Electrode active material and secondary battery

Inventors: Masaharu Sato (Nagaokakyo, JP); Toyonari Sugimoto (Sakai, JP); Takayuki Kubota (Amagasaki, JP); Takayuki Matsunaga (Amagasaki, JP)
Assignees: MURATA MANUFACTURING CO., LTD.; NARD INSTITUTE, LTD.
H01M4/60C07D487/14H01M4/604H01M4/608H01M10/0525
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Quick Facts
Patent No.
US 9,231,251
App. No.
13/852,468
Granted
Jan 5, 2016
Kind
B2
Abstract

An electrode active material is based on an organic compound containing in the structural unit thereof a pyrazine structure bound to cycloalkane. The electrode active material and a secondary battery containing it have large energy density, outputting high power, and having excellent cycle characteristics with little reduction in capacity even after repetition of charging and discharging.

Claims (23)

1. An electrode active material used as an active material in a secondary battery that is repeatedly charged and discharged by battery electrode reaction, comprising an organic compound containing a pyrazine structure bound to cycloalkane in the structural unit thereof.

2. The electrode active material according to claim 1 , wherein said organic compound is represented by the general formula:

in which R 1 and R 2 individually represent at least one member of the group consisting of a hydrogen atom, a substituted or unsubstituted C 1 -C 50 alkyl group, an aryl group, an aralkyl group, a cycloalkyl group, an alkoxyl group, an alkenyl group, an aryloxy group, an arylamino group, an alkylamino group, a thioaryl group, a thioalkyl group, a heterocyclic group, a formyl group, a silyl group, a boryl group, a stannyl group, a cyano group, a nitro group, a nitroso group, a carboxyl group, an alkoxycarbonyl group and a halogen atom, and R 1 and R 2 may be bound to each other to form a saturated or unsaturated ring, and n is an integer of 1 to 50.

3. The electrode active material according to claim 2 , in which R 1 and R 2 have a total combined molecular weight of up to about 250.

4. The electrode active material according to claim 1 which is selected from the group consisting of

5. The electrode active material according to claim 1 which is selected from the group consisting of

6. The electrode active material according to claim 1 , wherein said organic compound is represented by the general formula:

in which R 3 and R 4 individually represent at least one member of the group consisting of a hydrogen atom, a substituted or unsubstituted C 1 -C 50 alkyl group, an aryl group, an aralkyl group, a cycloalkyl group, an alkoxyl group, an alkenyl group, an aryloxy group, an arylamino group, an alkylamino group, a thioaryl group, a thioalkyl group, a heterocyclic group, a formyl group, a silyl group, a boryl group, a stannyl group, a cyano group, a nitro group, a nitroso group, a carboxyl group, an alkoxycarbonyl group and a halogen atom; X 1 represents CH 2 , CF 2 , O, S, Se, N—R′, P—R′, and As—R′ in which R′ represents at least one member of the group consisting of a hydrogen atom, a substituted or unsubstituted C1-C50 alkyl group, an aryl group, an aralkyl group, a cycloalkyl group, an alkoxyl group, an alkenyl group, an aryloxy group, an arylamino group, an alkylamino group, a thioaryl group, a thioalkyl group, a heterocyclic group, a silyl group, a boryl group, a stannyl group, a cyano group, a nitro group, a nitroso group, and a halogen atom, and R 3 , R 4 and X 1 may be bound to each other to form a saturated or unsaturated ring; and p and q are individually an integer of 1 to 50.

7. The electrode active material according to claim 1 , wherein said organic compound is represented by the general formula:

and

in which R 5 to R 10 individually represent at least one member of the group consisting of a hydrogen atom, a substituted or unsubstituted C1-C50 alkyl group, an aryl group, an aralkyl group, a cycloalkyl group, an alkoxyl group, an alkenyl group, an aryloxy group, an arylamino group, an alkylamino group, a thioaryl group, a thioalkyl group, a heterocyclic group, a formyl group, a silyl group, a boryl group, a stannyl group, a cyano group, a nitro group, a nitroso group, a carboxyl group, an alkoxycarbonyl group and a halogen atom, and may be bound to each other to form a saturated or unsaturated ring.

8. A secondary battery wherein the electrode active material according to claim 7 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

9. A secondary battery wherein the electrode active material according to claim 6 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

10. A secondary battery wherein the electrode active material according to claim 5 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

11. A secondary battery wherein the electrode active material according to claim 4 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

12. A secondary battery wherein the electrode active material according to claim 3 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

13. A secondary battery wherein the electrode active material according to claim 2 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

14. A secondary battery wherein the electrode active material according to claim 1 is present in at least one of a reaction starting substance, a product and an intermediate product during the discharging reaction of battery electrode reaction.

15. A secondary battery comprising a cathode, an anode, and an electrolyte, wherein said cathode comprises the electrode active material according to claim 1 .

16. A secondary battery comprising a cathode, an anode, and an electrolyte, wherein said cathode comprises the electrode active material according to claim 2 .

17. A secondary battery comprising a cathode, an anode, and an electrolyte, wherein said cathode comprises the electrode active material according to claim 3 .

18. A secondary battery comprising a cathode, an anode, and an electrolyte, wherein said cathode comprises the electrode active material according to claim 6 .

19. A secondary battery comprising a cathode, an anode, and an electrolyte, wherein said cathode comprises the electrode active material according to claim 7 .

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jun 13, 2018
From: MURATA MANUFACTURING CO., LTD.
To: NARD INSTITUTE, LTD.
Reel/Frame 046069/0820 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 28, 2013
From: SATO, MASAHARU; SUGIMOTO, TOYONARI; KUBOTA, TAKAYUKI; MATSUNAGA, TAKAYUKI
To: MURATA MANUFACTURING CO., LTD.; NARD INSTITUTE, LTD.
Reel/Frame 030108/0159 →
Priority Claims (1)
JP 2010-221851 · Sep 30, 2010 · national
Continuity (2)
Continuation PCTJP2011072398 · Sep 29, 2011
Related Publication 20130216909A1 · Aug 22, 2013