Electrolytes for magnesium electrochemical cells
US-2016308248-A1 · Oct 20, 2016 · US
US9985290B2 · US · B2
| Field | Value |
|---|---|
| Publication number | US-9985290-B2 |
| Application number | US-201615043888-A |
| Country | US |
| Kind code | B2 |
| Filing date | Feb 15, 2016 |
| Priority date | Feb 15, 2016 |
| Publication date | May 29, 2018 |
| Grant date | May 29, 2018 |
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Described is a salt of the general formula: Mg 2+ (L x ) 6 (PF 6 ) 2 wherein each L is a ligand selected from dichloromethane, a cyclic ether, or a nitrile of the general formula R—C≡N. The method of making the salt comprises the steps: providing Mg metal, activating the Mg metal in a first dry solution comprising a first ligand solution (L 1 ), treating the dry solution of activated Mg metal and L 1 with NOPF 6 in a second dry solution comprising a second ligand solution (L 2 ), heating the treated Mg metal solution removing residual solvent under vacuum, and recrystallizing the remaining solid to form the salt wherein L x comprises a mixture of L 1 and L 2 . The salt can be used as the salt in an electrolyte, or as an additive to an electrolyte, in a cell or battery.
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The invention claimed is: 1. A salt of the general formula: Mg 2+ (L) x (PF 6 ) 2 (i) wherein x represents a number between 1 and 6; and each L represents a ligand selected from one of the following compounds: a halomethane, a cyclic crown ether; or a nitrile of the general formula R—C≡N. 2. The salt of claim 1 , wherein x is greater than 1, and L represents a ligand selected from only one of the following compounds: a halomethane, a cyclic crown ether; or a nitrile of the general formula R—C≡N. 3. The salt of claim 2 , wherein each ligand L is acetonitrile. 4. The salt of claim 1 , wherein x is equal to 6, ligand L is a nitrile and R represents an organic group independently selected from the following: methyl, ethyl, propyl, butyl, t butyl, pentyl, ethylene, propylene, butylene, pentylene, toluene, naphthalene, or phenyl. 5. The salt of claim 4 , wherein R is the same for each ligand represented by L. 6. The salt of claim 1 , wherein x is equal to 1 and L is a cyclic crown ether selected from one of the following: [12]-crown-4, [18]-crown-6, [24]-crown-8. 7. The salt of claim 1 , wherein the halomethane is dichloromethane. 8. An electrolyte comprising the salt of claim 1 . 9. A cell comprising the electrolyte of claim 8 . 10. The cell of claim 9 , wherein the cell is a magnesium cell or a magnesium-ion cell. 11. A battery comprising the electrolyte of claim 8 . 12. The battery of claim 11 , wherein the battery is a magnesium battery or a magnesium-ion battery. 13. A method of making a salt of the general formula: Mg 2+ (L y ) x (PF 6 ) 2 (i) wherein x represent a number between 1 and 6, L y represents a ligand independently selected from any one of the following compounds: a halomethane, a cyclic crown ether; or a nitrile of the general formula R—C≡N; and L y comprises a mixture of compounds L 1 and L 2 ; the method comprising: providing Mg metal, washing and activating the Mg metal in a first dry solution comprising a first compound (L 1 ), treating the solution of activated Mg metal and first compound L 1 with NOPF 6 in a second dry solution comprising a second compound (L 2 ), removing the residual solvent, and recrystallizing the remaining solid to form the salt of Formula (i). 14. The method of claim 13 , wherein x is greater than 1, and L y represents a ligand selected from only one of the following compounds: a halomethane, a cyclic crown ether; or a nitrile of the general formula R—C≡N. 15. The method of claim 13 , wherein x is equal to 6, L 1 and L 2 are each nitriles, and for L 1 and L 2 R independently represents an organic group selected from the following: methyl, ethyl, propyl, butyl, t butyl, pentyl, ethylene, propylene, butylene, pentylene, toluene, naphthalene, or phenyl. 16. The method of claim 15 , wherein L 1 and L 2 are the same nitrile. 17. The method of claim 16 , wherein L 1 and L 2 are both acetonitrile. 18. The method of claim 13 , wherein x is equal to 1 and L y is a cyclic crown ether selected from one of the following: [12]-crown-4, [18]-crown-6, [24]-crown-8. 19. The method of claim 13 , wherein the halomethane is dichloromethane.
Accumulators with insertion or intercalation of metals other than lithium, e.g. with magnesium or aluminium · CPC title
characterised by the electrolyte · CPC title
of organic compounds · CPC title
by reactions not involving the formation of cyano groups · CPC title
Organic electrolyte · CPC title
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