Lithium metal negative electrode and method of manufacturing the same

Patent metadata

Field	Value
Publication number	US-12334561-B2
Application number	US-202117525096-A
Country	US
Kind code	B2
Filing date	Nov 12, 2021
Priority date	Nov 12, 2021
Publication date	Jun 17, 2025
Grant date	Jun 17, 2025

Abstract

A negative electrode for an electrochemical cell of a secondary lithium metal battery is manufactured by a method in which a precursor solution is applied to a major surface of a lithium metal substrate to form a protective interfacial layer thereon. The precursor solution includes a first organic solvent mixture, a dioxolane, and a fluorinated organosilane. The protective interfacial layer exhibits a composite structure including a polymeric matrix component and a lithium-containing dispersed component embedded in the polymeric matrix component.

First claim

What is claimed is:

1. A method of manufacturing a negative electrode for a secondary lithium metal battery, the method comprising:
applying a precursor solution to a major surface of a lithium metal substrate to form a protective interfacial layer thereon, the protective interfacial layer having a thickness in a range of 10 nanometers to 5 micrometers, a composite structure, and being chemically bonded to the lithium metal substrate via a plurality of silicon-oxygen bonds and alkoxide bonds, the composite structure including a polymeric matrix component and a lithium-containing dispersed component embedded in the polymeric matrix component, the polymeric matrix component comprising a plurality of siloxane bonds and the lithium-containing dispersed component comprising lithium fluoride,
wherein the precursor solution
applied to the major surface of the lithium metal substrate comprises an organic solvent, 10% to 50%, by weight, of a dioxolane, and 2% to 5%, by weight, of a fluorinated organosilane, the dioxolane being a chemical compound that contains a dioxolane ring, and the fluorinated organosilane having the formula: R′R″ n SiX 4-n , wherein n=0, 1, or 2, and wherein R′ is a polyfluorinated C 1 -C 8 alkyl group having greater than or equal to 3 and less than or equal to 13 fluorine atoms, R″ is H or a methyl group, and X is a methoxy group or a chlorine atom.

2. The method of claim 1 wherein the dioxolane is 1,3-dioxolane.

3. The method of claim 1 wherein the fluorinated organosilane is at least one of (3,3,3-trifluoropropylmethyl) dimethoxysilane, (3,3,3-Trifluoropropyl) trimethoxysilane, 1H,1H,2H,2H-perfluorooctylmethyldimethoxysilane, 1H, 1H,2H,2H-perfluorooctyltrimethoxysilane, 1H, 1H,2H,2H-perfluorooctyldimethylchlorosilane, perfluorooctylmethyldichlorosilane, 1H,1H,2H,2H- (1H,1H,2H,2H-perfluoro-n- hexyl) methyldichlorosilane, or 1H, 1H,2H,2H-perfluorooctyltrichlorosilane.

4. The method of claim 1 wherein the organic solvent mixture comprises a mixture of an acyclic ether and a cyclic ether, optionally wherein the organic solvent mixture comprises a mixture of 1,2-dimethoxyethane and tetrahydrofuran.

5. The method of claim 1 further comprising:
removing unreacted dioxolane compounds, fluorinated organosilane compounds, and/or mobile reaction byproducts from the protective interfacial layer,
optionally wherein the unreacted dioxolane compounds, fluorinated organosilane compounds, and/or mobile reaction byproducts are removed from the protective interfacial layer by washing the protective interfacial layer with a nonpolar organic solvent.

6. A lithium metal battery, comprising:
a positive electrode including a transition metal oxide that can undergo a reversible intercalation of lithium ions;
a lithium metal negative electrode spaced apart from the positive electrode, the lithium metal negative electrode including a lithium metal layer disposed on a negative electrode current collector, the lithium metal layer having a major facing surface that faces toward the positive electrode; a nonaqueous liquid electrolyte in ionic contact with the positive electrode and the lithium metal negative electrode; and
a protective interfacial layer formed directly on the major facing surface of the lithium metal layer, along an interface between the lithium metal negative electrode and the nonaqueous liquid electrolyte, the protective interfacial layer having a thickness in a range of 10 nanometers to 5 micrometers, a composite structure, and being chemically bonded to the lithium metal layer via a plurality of silicon-oxygen bonds and alkoxide bonds, the composite structure including a polymeric matrix component and a lithium-containing dispersed component embedded in the polymeric matrix component, the polymeric matrix component comprising a plurality of siloxane bonds and the lithium-containing dispersed component comprising lithium fluoride,
wherein the protective interfacial layer is formed on the major facing surface of the lithium metal layer prior to assembly of the lithium metal battery by applying a precursor solution to the lithium metal layer, the precursor solution comprising an organic solvent, 10% to 50%, by weight, of a dioxolane, and 2% to 5%, by weight, of a fluorinated organosilane having the formula: R′R″ n SiX 4-n , wherein n=0,1, or 2, and wherein R′ is a polyfluorinated C 1 -C 8 alkyl group having greater than or equal to 3 and less than or equal to 13 fluorine atoms, R″ is H or a methyl group, and X is a methoxy group or a chlorine atom.

7. The electrochemical cell of claim 6 wherein the lithium metal layer comprises, by weight, greater than 97% lithium.

8. The electrochemical cell of claim 6 wherein the transition metal oxide of the positive electrode is a high-nickel content lithium nickel cobalt manganese oxide having the chemical formula: LiNi 1-a-b CoaMn b O 2 , wherein a=0.1-0.2 and b=0.1-0.2.

9. The electrochemical cell of claim 6 wherein the nonaqueous liquid electrolyte comprises a nonaqueous aprotic organic solvent and a lithium salt dissolved in the nonaqueous aprotic organic solvent.

10. The battery of claim 6 wherein the fluorinated organosilane comprises (3,3,3-trifluoropropylmethyl) dimethoxysilane, (3,3,3-Trifluoropropyl) trimethoxysilane, 1H,1H,2H,2H-perfluorooctylmethyldimethoxysilane, 1H,1H,2H,2H-perfluorooctyltrimethoxysilane, 1H, 1H,2H,2H-perfluorooctyldimethylchlorosilane, 1H, 1H,2H,2H-perfluorooctylmethyldichlorosilane, (1H,1H,2H,2H-perfluoro-n-hexyl) methyldichlorosilane, and/or 1H, 1H,2H,2H-perfluorooctyltrichlorosilane.

11. The battery of claim 6 wherein the fluorinated organosilane comprises at least one fluorinated chlorosilane selected from the group consisting of 1H,1H,2H,2H-perfluorooctyldimethylchlorosilane; 1H,1H,2H,2H-perfluorooctylmethyldichlorosilane;
(1H,1H,2H,2H-perfluoro-n-hexyl) methyldichlorosilane; and 1H,1H,2H,2H-perfluorooctyltrichlorosilane.

12. The battery of claim 6 wherein R′ is a polyfluorinated C 3 -C 6 alkyl group having greater than or equal to 3 and less than or equal to 9 fluorine atoms.

13. The battery of claim 6 wherein the fluorinated organosilane comprises (3,3,3-trifluoropropylmethyl) dimethoxysilane and/or (3,3,3-Trifluoropropyl) trimethoxysilane.

14. The battery of claim 6 wherein the dioxolane comprises 4,5-diethyl-dioxolane; 4,5-dimethyl-dioxolane; 4-methyl-1,3-dioxolane; and/or 4-ethyl-1,3-dioxolane.

15. The battery of claim 6 wherein the protective interfacial layer has a porosity of about 60%.

Assignees

• Gm Global Tech Operations Llc

Inventors

• Okada Kanako
• Roy Jesse M
• Yang Li
• Fortier Mary E

Classifications

• H01M4/0402

  Methods of deposition of the material · CPC title

• H01M4/525

  of mixed oxides or hydroxides containing iron, cobalt or nickel for inserting or intercalating light metals, e.g. LiNiO2, LiCoO2 or LiCoOxFy · CPC title

• H01M4/505

  of mixed oxides or hydroxides containing manganese for inserting or intercalating light metals, e.g. LiMn2O4 or LiMn2OxFy · CPC title

• H01M10/052

  Li-accumulators · CPC title

• H01M2300/0025

  Organic electrolyte · CPC title