Secondary battery and method for charging and discharging secondary battery

US9711824B2 · US · B2

Patent metadata
FieldValue
Publication numberUS-9711824-B2
Application numberUS-201514707384-A
CountryUS
Kind codeB2
Filing dateMay 8, 2015
Priority dateNov 9, 2012
Publication dateJul 18, 2017
Grant dateJul 18, 2017

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  1. Title

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  2. Abstract

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  3. Assignees and inventors

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  4. Key dates

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  5. First independent claim

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  6. CPC / IPC classifications

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  7. Citations and related patents

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Abstract

Official abstract text for this publication.

A secondary battery that has an electrode active material mainly composed of a low-molecular-weight multi-electron organic compound that has two or more electrons to be involved in a battery electrode reaction, and a solvent for an electrolyte solution that contains a sulfone compound. Apart of the electrode active material is dissolved in and reacted with the electrolyte solution at the first charge and discharge, thereby oligomerizing a part of the electrode active material.

First claim

Opening claim text (preview).

The invention claimed is: 1. A secondary battery comprising: an electrode active material; and an electrolyte solution having an electrolyte salt in a solvent, wherein the electrode active material contains, as a main component thereof, a multi-electron organic compound which has two or more electrons to be involved in a battery electrode reaction, the solvent contains a sulfone compound, and a part of the electrode active material is oligomerized at least at a first time of charge and discharge of the secondary battery. 2. The secondary battery according to claim 1 , wherein the sulfone compound is represented by the general formula: wherein R 1 and R 2 are at least one of a linear alkyl group and a branched alkyl group respectively having 1 to 5 carbon atoms. 3. The secondary battery according to claim 2 , wherein R 1 and R 2 are the same or are linked with each other to forma saturated or unsaturated ring. 4. The secondary battery according to claim 1 , wherein the multi-electron organic compound contains, in structural unit thereof, at least one selected from the group consisting of dithione compounds having a dithione structure, dione compounds having a dione structure, and diamine compounds having a diamine structure. 5. The secondary battery according to claim 4 , wherein the dithione compound is represented by the general formula: wherein R 3 and R 4 are any of a substituted or unsubstituted amino group, a substituted or unsubstituted imino group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkylene group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkoxyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted thioaryl group, a substituted or unsubstituted thioalkyl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted formyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted cyano group, a substituted or unsubstituted nitro group, a substituted or unsubstituted nitroso group, a substituted or unsubstituted carboxyl group, a substituted or unsubstituted alkoxycarbonyl group, and linking groups composed of combination of one or more thereof. 6. The secondary battery according to claim 5 , wherein R 3 and R 4 are the same or are linked with each other to forma saturated or unsaturated cyclic structure. 7. The secondary battery according to claim 4 , wherein the dithione compound is represented by the general formula: wherein R 5 and R 7 are any of a substituted or unsubstituted amino group, a substituted or unsubstituted imino group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkylene group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkoxyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted thioaryl group, a substituted or unsubstituted thioalkyl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted formyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted cyano group, a substituted or unsubstituted nitro group, a substituted or unsubstituted nitroso group, a substituted or unsubstituted carboxyl group, a substituted or unsubstituted alkoxycarbonyl group and linking groups composed of combination of one or more thereof, and R 6 is at least one of a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group and a substituted or unsubstituted imino group. 8. The secondary battery according to claim 7 , wherein R 5 and R 7 are the same or are linked with each other to forma saturated or unsaturated cyclic structure. 9. The secondary battery according to claim 7 , wherein R 6 is the substituted or unsubstituted imino groups, and the imino groups are linked with each other. 10. The secondary battery according to claim 4 , wherein the dione compound is represented by the general formula: wherein R 8 and R 9 are any of a substituted or unsubstituted amino group, a substituted or unsubstituted imino group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkylene group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkoxyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted thioaryl group, a substituted or unsubstituted thioalkyl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted formyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted cyano group, a substituted or unsubstituted nitro group, a substituted or unsubstituted nitroso group, a substituted or unsubstituted carboxyl group, a substituted or unsubstituted alkoxycarbonyl group and linking groups composed of combination of one or more thereof. 11. The secondary battery according to claim 10 , wherein R 8 and R 9 are the same or are linked with each other to forma saturated or unsaturated cyclic structure. 12. The secondary battery according to claim 4 , wherein the dione compound is represented by the general formula: wherein R 10 and R 12 are any of a substituted or unsubstituted amino group, a substituted or unsubstituted imino group, a substituted or unsubstituted alkyl group, a substituted or unsubstituted alkylene group, a substituted or unsubstituted aryl group, a substituted or unsubstituted aralkyl group, a substituted or unsubstituted cycloalkyl group, a substituted or unsubstituted alkoxyl group, a substituted or unsubstituted alkenyl group, a substituted or unsubstituted aryloxy group, a substituted or unsubstituted arylamino group, a substituted or unsubstituted alkylamino group, a substituted or unsubstituted thioaryl group, a substituted or unsubstituted thioalkyl group, a substituted or unsubstituted heterocyclic group, a substituted or unsubstituted formyl group, a substituted or unsubstituted silyl group, a substituted or unsubstituted cyano group, a substituted or unsubstituted nitro group, a substituted or unsubstituted nitroso group, a substituted or unsubstituted carboxyl group, a substituted or unsubstituted alkoxycarbonyl group and linking groups composed of combination of one or more thereof, and R 11 is at least one of a substituted or unsubstituted alkylene group, a substituted or unsubstituted arylene group and a substituted or unsubstituted imino

Assignees

Inventors

Classifications

  • of electrodes based on electro-active polymers · CPC title

  • Li-accumulators · CPC title

  • Methods for charging or discharging (circuits for charging H02J7/00) · CPC title

  • Polymers · CPC title

  • Batteries in portable systems, e.g. mobile phone, laptop · CPC title

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What does patent US9711824B2 cover?
A secondary battery that has an electrode active material mainly composed of a low-molecular-weight multi-electron organic compound that has two or more electrons to be involved in a battery electrode reaction, and a solvent for an electrolyte solution that contains a sulfone compound. Apart of the electrode active material is dissolved in and reacted with the electrolyte solution at the first …
Who is the assignee on this patent?
Murata Manufacturing Co, Carlit Holdings Co Ltd
What technology area does this patent fall under?
Primary CPC classification H01M10/0569. Mapped technology areas include Electricity.
When was this patent published?
Publication date Tue Jul 18 2017 00:00:00 GMT+0000 (Coordinated Universal Time) (B2). Legal status and post-grant events are not shown on this page.
What related patents are in patentsdb?
We list 8 related publications on this page (citations in our corpus or others sharing the same primary CPC).