Liquid Electrolyte Composition, and Electrochemical Cell Comprising Said Electrolyte Composition
US-2024347772-A1 · Oct 17, 2024 · US
US10826121B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-10826121-B2 |
| Application number | US-201815891197-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 7, 2018 |
| Priority date | Feb 7, 2017 |
| Publication date | Nov 3, 2020 |
| Grant date | Nov 3, 2020 |
A practical reading order for non-experts. Skip the full description unless you need deep technical detail.
What the patent document calls the invention.
A short plain-language summary of the technical disclosure.
Who owns or filed the patent and who is credited as inventor.
Filing, priority, publication, and grant dates set the timeline.
The legal scope of protection — read this for what is actually claimed.
Technology tags used to group this patent with similar filings.
Prior art links and similar publications in this corpus.
Official abstract text for this publication.
The present disclosure provides an electrolyte and a secondary battery. The electrolyte comprises: a non-aqueous organic solvent; an electrolyte salt dissolved in the non-aqueous organic solvent; and an additive dissolved in the non-aqueous organic solvent. The additive comprises a first additive, the first additive is selected from boron phosphate represented by formula 1. When the electrolyte of the present disclosure is applied in the secondary battery, the performances of the secondary battery under high temperature environment can be effectively improved.
Opening claim text (preview).
What is claimed is: 1. An electrolyte, comprising: a non-aqueous organic solvent; an electrolyte salt dissolved in the non-aqueous organic solvent; and an additive dissolved in the non-aqueous organic solvent; the additive comprising a first additive, the first additive being selected from boron phosphate represented by formula 1; and the additive further comprising a second additive, the second additive being C—C double bond-containing cyclic carbonate ester, wherein the C—C double bond-containing cyclic carbonate ester is one or more selected from the group consisting of compounds represented by formula 10, R 33 ˜R 34 are independently selected from the group consisting of H, halogen atom, substituted or unsubstituted C1˜C10 alkyl, substituted or unsubstituted C2˜C10 alkenyl, substituted or unsubstituted C2˜C10 alkynyl and substituted or unsubstituted C6˜C10 aryl; wherein a mass of the second additive is 0.01%˜5% of a total mass of the electrolyte. 2. The electrolyte according to claim 1 , wherein the second additive is: 3. The electrolyte according to claim 1 , wherein a mass of the first additive is 0.01%˜5% of a total mass of the electrolyte. 4. The electrolyte according to claim 1 , wherein the non-aqueous organic solvent comprises: one or more selected from a group consisting of ethylene carbonate, propylene carbonate, 2,3-butylene carbonate, γ-butyrolactone and fluoroethylene carbonate; and one or more selected from a group consisting of dimethyl carbonate, diethyl carbonate, dipropyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, ethyl propyl carbonate, methyl formate, ethyl formate, propyl formate, methyl acetate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate and propyl propionate. 5. The electrolyte according to claim 1 , wherein a molar concentration of the electrolyte salt in the electrolyte is 0.01 mol/L˜3 mol/L. 6. A secondary battery comprising an electrolyte, the electrolyte comprising: a non-aqueous organic solvent; an electrolyte salt dissolved in the non-aqueous organic solvent; and an additive dissolved in the non-aqueous organic solvent; the additive comprising a first additive, the first additive being selected from boron phosphate represented by formula 1; and the additive further comprising a second additive, the second additive being C—C double bond-containing cyclic carbonate ester, wherein the C—C double bond-containing cyclic carbonate ester is one or more selected from the group consisting of compounds represented by formula 10, R 33 ˜R 34 are independently selected from the group consisting of H, halogen atom, substituted or unsubstituted C1˜C10 alkyl, substituted or unsubstituted C2˜C10 alkenyl, substituted or unsubstituted C2˜C10 alkynyl and substituted or unsubstituted C6˜C10 aryl; wherein a mass of the second additive is 0.01%˜5% of a total mass of the electrolyte. 7. The secondary battery according to claim 6 , wherein the second additive is: 8. The secondary battery according to claim 6 , wherein a mass of the first additive is 0.01%˜5% of a total mass of the electrolyte. 9. The secondary battery according to claim 6 , wherein the non-aqueous organic solvent comprises: one or more selected from a group consisting of ethylene carbonate, propylene carbonate, 2,3-butylene carbonate, γ-butyrolactone and fluoroethylene carbonate; and one or more selected from a group consisting of dimethyl carbonate, diethyl carbonate, dipropyl carbonate, ethyl methyl carbonate, methyl propyl carbonate, ethyl propyl carbonate, methyl formate, ethyl formate, propyl formate, methyl acetate, ethyl acetate, propyl acetate, methyl propionate, ethyl propionate and propyl propionate. 10. The secondary battery according to claim 6 , wherein a molar concentration of the electrolyte salt in the electrolyte is 0.01 mol/L˜3 mol/L.
Organic electrolyte · CPC title
characterised by the solvents · CPC title
characterised by the additives · CPC title
Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title
Energy storage using batteries · CPC title
Related publications grouped by family.
Answers are generated from the same data shown on this page.