High voltage redox shuttles, method for making high voltage redox shuttles

Patent metadata

Field	Value
Publication number	US-10008743-B2
Application number	US-201414171556-A
Country	US
Kind code	B2
Filing date	Feb 3, 2014
Priority date	Feb 3, 2014
Publication date	Jun 26, 2018
Grant date	Jun 26, 2018

Abstract

The invention provides a method for producing a molecule capable of undergoing reduction-oxidation when subjected to a voltage potential, the method comprising phosphorylating hydroquinone to create a first intermediate; rearranging the first intermediate to an aryl-bis-(phosphonate) thereby creating a second intermediate comprising phosphorous alkoxy groups; alkylating (e.g., methylating) the second intermediate; converting the alkoxy groups to halides; and substituting the halides to alkyl or aryl groups. Also provided is a system for preventing overcharge in a Lithium-ion battery, the method comprising a mixture of a redox shuttle with electrolyte in the battery such that the shuttle comprises between about 10 and about 20 weight percent of the mixture.

First claim

The embodiment of the invention in which an exclusive property or privilege is claimed is defined as follows:

1. A method for producing a molecule capable of undergoing reduction-oxidation when subjected to a voltage potential, the method comprising:
a. phosphorylating hydroquinone to create a first intermediate compound;
b. rearranging the first intermediate compound to an aryl-bis-(phosphonate) thereby creating a second intermediate compound comprising phosphorous alkoxy groups;
c. alkylating the second intermediate compound;
d. converting the alkoxy groups to halides; and
e. substituting the halides to alkyl or aryl groups; wherein the entire method is performed at or above a lowest temperature wherein said lowest temperature is between approximately −10° C. and approximately −20° C.

2. The method as recited in claim 1 wherein at least four phosphorous alkoxy groups are converted to halides.

3. The method as recited in claim 1 further comprising a recrystallization step to produce the molecule having better than 99 percent purity.

4. The method as recited in claim 1 wherein step c is performed at or below a highest temperature, the highest temperature about 60° C.

5. The method as recited in claim 1 wherein the highest natural reaction temperature for the conversion step is between about 75 and about 80 C.

6. The method as recited in claim 1 wherein the alkoxy groups are phosphonate esters which are chlorinated to yield aryl bis(phosphonyl dichloride).

7. The method as recited in claim 1 wherein the halide is aryl bis(phosphonyl dichloride) and the dichloride does not need to be purified prior to the substitution step.

8. The method as recited in claim 1 wherein each of the alkyl groups bonded to phosphorous contain no more than 2 carbons.

9. The molecule as produced by the method of claim 1 , whereby the molecule exhibits between about 10 and about 20 weight percent solubility in an electrolyte of a Lithium-ion battery.

10. The method of claim 1 wherein hydroquinone is 1-4 dihydroxy benzene.

11. The method of claim 1 wherein part c. is performed using solvents.

12. The method of claim 1 wherein the lowest temperature is about −15° C.

Assignees

• Krumdick Gregory K
• Dzwiniel Trevor L
• Pupek Krzysztof
• Uchicago Argonne Llc

Inventors

• Krumdick Gregory K
• Dzwiniel Trevor L
• Pupek Krzysztof

Classifications

• H01M10/0567 Primary

  characterised by the additives · CPC title

• H01M10/4235

  Safety or regulating additives or arrangements in electrodes, separators or electrolyte (H01M10/4242 takes precedence) · CPC title

• C07F9/4021

  Esters of aromatic acids (P-C aromatic linkage) · CPC title

• H01M2300/0025

  Organic electrolyte · CPC title

• H01M10/0525

  Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries · CPC title