Method for removing lithium hydride faceted defects from lithium metal foil
In this disclosure, we describe a new chemical treatment that can be performed on lithium metal and lithium alloy surfaces to selectively remove LiH defects. This treatment utilizes an exclusive reaction between LiH and trialkyl borane to form lithium borohydride complexes, which can be easily washed away from surface using an inert organic solvent. This treatment can be useful for lithium metal and lithium alloy anodes for high energy batteries.
1. A method, comprising the steps of:
providing a lithium foil that has a first surface wherein the first surface contains LiH defects;
placing the lithium foil in a solution of a trialkyl borane and a solvent for 0.25-4 hours, the trialkyl borane has a structure as follows:
wherein each R is selected independently from the group consisting of alkyl groups, perfluoroalkyl groups, alkoxy groups, and perfluoro alkoxy groups, and the perfluoroalkyl groups are selected from the group consisting of CF 3 , CF 2 CF 3 , and combinations thereof;
removing the lithium foil from the solution; and
rinsing the lithium foil in a solvent.
2. The method of claim 1 wherein the alkyl groups are selected from the group consisting of methyl, ethyl, propyl, butyl, iso-propyl, tert-butyl, phenyl, cyclohexyl, allyl, and vinyl groups, and combinations thereof.
3. The method of claim 1 wherein at least one R is selected from the perfluoroalkyl groups.
4. The method of claim 1 , wherein the solvent is selected from the group consisting of hexane, heptane, tetrahydrofuran (THF), and ether.
5. The method of claim 1 wherein the solvent is an inert organic solvent.
6. The method of claim 1 wherein the first surface includes a surface coverage of LiH defects of less than 1%.
7. The method of claim 1 wherein the solvent is tetrahydrofuran.
8. A method, comprising the steps of:
providing a lithium foil that has a first surface wherein the first surface contains LiH defects;
placing the lithium foil in a solution of a trialkyl borane and a solvent for 0.25-4 hours, the trialkyl borane has a structure as follows:
wherein each R is selected independently from the group consisting of alkyl groups, perfluoroalkyl groups, alkoxy groups, and perfluoro alkoxy groups, and the alkoxy groups are selected from the group consisting of methoxy, ethoxy, and isopropoxy groups, and combinations thereof;
removing the lithium foil from the solution; and
rinsing the lithium foil in a solvent.
9. The method of claim 8 wherein at least one R is selected from the alkoxy groups.
10. The method of claim 8 wherein the alkyl groups are selected from the group consisting of methyl, ethyl, propyl, butyl, iso-propyl, tert-butyl, phenyl, cyclohexyl, allyl, and vinyl groups, and combinations thereof.
11. The method of claim 8 wherein the solvent is an inert organic solvent.
12. The method of claim 8 wherein the solvent is selected from the group consisting of hexane, heptane, tetrahydrofuran (THF), and ether.
13. The method of claim 8 wherein the alkyl groups are selected from the group consisting of methyl, ethyl, propyl, butyl, iso-propyl, tert-butyl, phenyl, cyclohexyl, allyl, and vinyl groups, and combinations thereof.
14. The method of claim 8 wherein the first surface includes a surface coverage of LiH defects of less than 1%.
15. A method, comprising the steps of:
providing a lithium foil that has a first surface wherein the first surface contains LiH defects;
placing the lithium foil in a solution of a trialkyl borane and a solvent for 0.25-4 hours, the trialkyl borane has a structure as follows:
wherein each R is selected independently from the group consisting of alkyl groups, perfluoroalkyl groups, alkoxy groups, and perfluoro alkoxy groups, and the perfluoro alkoxy groups are selected from the group consisting of CF 3 O—, CF 2 CF 3 O—, and combinations thereof;
removing the lithium foil from the solution; and
rinsing the lithium foil in a solvent.
16. The method of claim 15 wherein at least one R is selected from the perfluoro alkoxy groups.
17. The method of claim 15 wherein the solvent is an inert organic solvent.
18. The method of claim 15 wherein the solvent is selected from the group consisting of hexane, heptane, tetrahydrofuran (THF), and ether.
19. The method of claim 15 wherein the alkyl groups are selected from the group consisting of methyl, ethyl, propyl, butyl, iso-propyl, tert-butyl, phenyl, cyclohexyl, allyl, and vinyl groups, and combinations thereof.
20. The method of claim 15 wherein the first surface includes a surface coverage of LiH defects of less than 1%.