Chloride-free electrolyte for a magnesium battery and a method to convert a magnesium electrolyte to a chloride-free electrolyte

Patent metadata

Field	Value
Publication number	US-10147970-B2
Application number	US-201414263392-A
Country	US
Kind code	B2
Filing date	Apr 28, 2014
Priority date	Apr 28, 2014
Publication date	Dec 4, 2018
Grant date	Dec 4, 2018

Abstract

A method to prepare a chloride free magnesium electrolyte salt is provided. According to the method a water stable borate or carborate anion is converted to metal salt of an alkali metal or silver by an ion exchange and then converted to a chloride free magnesium salt by another ion exchange. A chloride free magnesium salt suitable as an electrolyte for a magnesium battery and a magnesium battery containing the chloride free magnesium electrolyte are also provided.

First claim

The invention claimed is:

1. A method to prepare a nonaqueous magnesium electrolyte, the nonaqueous magnesium electrolyte comprising:
a nonaqueous solvent comprising an ether oxygen; and
a magnesium salt of formula (I):
[A] 2 Mg(Solvent)) y   (I)

wherein
the electrolyte does not comprise chloride ions,
Solvent is the nonaqueous solvent comprising the ether oxygen and y is an integer of 2 to 6, and
A is at least one of a water stable borate anion or a water stable carborate anion;
the method comprising:
reacting a Grignard reagent of formula RMgCl with i) a borane of formula BR 3 wherein each R is independently selected from the group consisting of an alkyl group of 1-6 carbon atoms, optionally substituted with F, an aryl group optionally substituted with F, and an alkylphenyl group optionally substituted with F; or ii) a carborane of formula C 2 B 10 H 12 in tetrahydrofuran to obtain a magnesium salt of formula:
[Mg 2 (μ-Cl) 3 .6THF]A

wherein A is i) a borate anion of formula BR 4 − (II) wherein each R is independently selected from the group consisting of an alkyl group of 1-6 carbon atoms, optionally substituted with F, an aryl group optionally substituted with F, and an alkylphenyl group optionally substituted with F; or ii) a carborate anion of formula C 2 B 10 H 11 − (III);
forming a M + salt of the anion A in an aqueous medium according to:
3[Mg 2 (μ-Cl) 3 .6THF]A+M 2 CO 3 /MHCO 3 (aq)→3MA+[Mg 2 (μ-Cl) 3 .6THF] 2 (CO 3 ) +[Mg 2 (μ-Cl) 3 .6THF](HCO 3 ):

extracting the MA salt from the aqueous medium;
isolating the free MA salt from the extract; and
ion exchange of Mg 2+ for the metal ion M + of the MA salt to obtain the Mg salt of formula (I),
wherein the metal ion (M + ) is at least one selected from the group consisting of Li + , Na + , K + Rb + , Cs + and Ag + .

2. The method according to claim 1 , wherein M + is Ag + .

3. The method according to claim 1 , wherein M + is K + .

4. The method according to claim 3 , wherein
the KA salt is extracted in ether; and
the KA salt is isolated by removing the ether under vacuum.

5. The method according to claim 4 , further comprising:
forming a Ag + salt of the anion A according to the exchange (b) in a medium wherein KNO 3 is insoluble:
KA+AgNO 3 →AgA+KNO 3 (s)  (b);

and
removing the precipitated KNO 3 (s) from the solution of the AgA salt.

6. The method according to claim 1 , wherein the borate anion of formula BR 4 − (II) is an anion of formula (IV):
[BPh 4 ] −   (IV)

wherein each Ph group is independently selected from the group consisting of an aryl group optionally substituted with F, and an alkyphenyl group optionally substituted with F.

7. The method according to claim 6 , wherein the borate anion of formula (IV) is the anion of formula (V):
[(C 6 F 5 ) 3 B(C 6 H 5 )] −   (V).

8. The method according to claim 6 , wherein the borate anion of formula (IV) is the anion of formula (VI):
[(Mes) 3 B(C 6 H 5 )] −   (VI)

wherein Mes is a 3,5-dimethylphenyl group.

9. The method according to claim I wherein A is the carborate anion of formula (III):
(C 2 B 10 H 11 ) −   (III)

wherein the carborate anion is an anion of an ortho-carborane, an anion of a meta-carborane or an anion of a para-carborane.

10. The method according to claim 1 , wherein the nonaqueous solvent comprising an ether oxygen is at least one of tetrahydrofuran (THF), dimethoxyethane (DME) and diethylene glycol dimethyl ether (diglyme) (DGM).

11. A method to prepare a magnesium electrolyte, comprising:
tetrahydrofuran; and
a salt of formula (VII):
[(C 6 F 5 ) 3 B(C 6 H 5 )] 2 Mg(THF) 6   (VII)

wherein THF is a tetrahydrofuran molecule,
the method comprising:

reacting a Grignard reagent of formula C 6 H 5 MgCl with a borane of formula B(C 6 F 5 ) 3 in tetrahydrofuran to obtain a magnesium salt of formula:
[Mg 2 (μ-Cl) 3 .6THF][(C 6 H 5 )B(C 6 F 5 ) 3 ]

forming a K + salt of the anion (C 6 H 5 )B(C 6 F 5 ) 3 in an aqueous medium according to:
3[Mg 2 (μ-Cl) 3 .6THF][(C 6 H 5 )B(C 6 F 5 ) 3 )]+K 2 CO 3 /KHCO 3 (aq)→3K[(C 6 H 5 )B(C 6 F 5 ) 3 )]+[Mg 2 (μ-Cl) 3 .6THF] 2 (CO 3 )+[Mg 2 (μ-Cl) 3 .6THF](HCO 3 ):

forming a Ag + salt of the anion (C 6 H 5 )B(C 6 F 5 ) 3 − according to the exchange (b) in a medium wherein KNO 3 is insoluble:
K[(C 6 H 5 )B(C 6 F 5 ) 3 ]+AgNO 3 →Ag[(C 6 H 5 )B(C 6 F 5 ) 3 ]+KNO 3 (s)  (b);

and
removing the precipitated KNO 3 (s) from the solution of the Ag[(C 6 H 5 )B(C 6 F 5 ) 3 ] salt
ion exchange of Mg for Ag in THF according to the equation:
2((C 6 H 5 )B(C 6 F 5 ) 3 )Ag+MgBr 2 →((C 6 H 5 )B(C 6 F 5 ) 3 ) 2 Mg(THF) 6 +2AgBr

and removal of the AgBr from the magnesium electrolyte,

wherein the magnesium electrolyte does not comprise a chloride ion.

12. A method to prepare a magnesium electrolyte, comprising:
tetrahydrofuran; and
a salt of formula (VIII):
[(Mes) 3 B (C 6 H 5 ) 3 ] 2 Mg(THF) 6   (VIII)

wherein

THF is a tetrahydrofuran molecule,
and
Mes is a 3,5-dimethylphenyl group,
the method comprising:

reacting a Grignard reagent of formula C 6 H 5 MgCl with a borane of formula
B(Mes) 3 in tetrahydrofuran to obtain a magnesium salt of formula:
[Mg 2 (μ-Cl) 3 6THF][(C 6 H 5 )B(Mes) 3 ]

forming a K + salt of the anion (C 6 H 5 )B(Mes) 3 in an aqueous medium according to:
3[Mg 2 (μ-Cl) 3 .6THF][(C 6 H 5 )B(Mes) 3 )]+K 2 CO 3 /KHCO 3 (aq)→3K[(C 6 H 5 )B(Mes) 3 )]+[Mg 2 (μ-Cl) 3 .6THF] 2 (CO 3 )+[Mg 2 (μ-Cl) 3 .6THF](HCO 3 ):

forming a Ag + salt of the anion (C 6 H 5 )B(Mes) 3 − according to the exchange (b) in a medium wherein KNO 3 is insoluble:
K((C 6 H 5 )B(Mes) 3 +AgNO 3 →Ag[(C 6 H 5 )B(C 6 F 5 ) 3 ]+KNO 3 (s)  (b);

and
removing the precipitated KNO 3 (s) from the solution of the Ag[(C 6 H 5 )B(Mes) 3 ] salt
ion exchange of Mg for Ag in THF according to the formula:
2((C 6 H 5 )B(Mes) 3 )Ag+MgBr 2 →((C 6 H 5 )B(Mes) 3 ) 2 Mg(THF) 6 +2AgBr

and removal of the AgBr from the magnesium electrolyte,

wherein the magnesium electrolyte does not comprise a chloride ion.

13. A magnesium electrolyte obtained according to the method of claim 1 , comprising:
a nonaqueous solvent comprising an ether oxygen; and
a salt of formula (I):
[A] 2 Mg(Solvent) y   (I)

wherein
Solvent is the nonaqueous solvent comprising the ether oxygen and is at least one selected from the group consisting of tetrahydrofuran, 2-methyl tetrahydrofuran, dimethoxyethane, glyme, monoglyme, dimethyl glycol, ethylene glycol dimethyl ether, diethyl ether, ethyl glyme, diglyme, proglyme, ethyl diglyme, triglyme, butyl diglyme, tetraglyme, polyglyme and higlyme,
y is an integer of 2 to 6,
A is a water stable borate anion or a water stable carborate anion selected from the group of anions consisting of:
(BR 4 ) −   (II)

wherein the R groups are each independently selected from the group consisting of an alkyl group of 1-6 carbon atoms, optionally substituted with F, an aryl group optionally substituted with F, and an alkylphenyl group optionally substituted with F and
(C 2 B 10 H 11 ) −   (III)

and
the magnesium electrolyte is free of chlorides.

14. A magnesium battery, comprising:
a negative electrode comprising magnesium;
a positive electrode ; and
the magnesium electrolyte according to claim 13 .

15. The magnesium battery, according to claim 14 ,
wherein the negative electrode is magnesium.

16. The magnesium battery, according to claim 14 , wherein
the positive electrode active material comprises at least one component selected from the group consi

Assignees

• Toyota Eng & Mfg North America

Inventors

• Muldoon John G
• Bucur Claudiu B

Classifications

• H01M2300/0037

  Mixture of solvents · CPC title

• H01M10/0569 Primary

  characterised by the solvents · CPC title

• H01M2300/0028

  characterised by the solvent · CPC title

• H01M4/54

  of silver · CPC title

• H01M4/58

  of inorganic compounds other than oxides or hydroxides, e.g. sulfides, selenides, tellurides, halogenides or LiCoFy; of polyanionic structures, e.g. phosphates, silicates or borates · CPC title