Lithium ion battery electrode materials and methods of making the same

1. A method for forming a lithium ion battery electrode material, the method comprising:

positioning a substrate precursor and a carbon precursor in a heating device such that the substrate precursor and the carbon precursor are carried in a direction of a gas flow through the heating device, wherein the carbon precursor is a solid or a liquid and wherein the substrate precursor is a metal oleate;

heating the carbon precursor to a temperature above its boiling point, thereby evaporating the carbon precursor and generating a vapor of the carbon precursor, the carbon precursor being selected from the group consisting of aromatic hydrocarbons and aromatic functional groups containing silanes; and exposing the substrate precursor to the vapor and an elevated temperature that is above the boiling point of the carbon precursor under an inert gas flow flowing in the direction, thereby forming a substrate and a carbon layer on the substrate.

2. The method as defined in claim 1 , further comprising synthesizing the substrate using an aerosol-assisted process.

3. The method as defined in claim 2 wherein synthesizing the substrate using the aerosol-assisted process is accomplished by:

atomizing a solution of the substrate precursor material in a liquid to form droplets of the substrate precursor material in the liquid; and

passing the droplets through a heating zone to convert the droplets to the substrate.

4. The method as defined in claim 3 wherein the substrate precursor material is a metal oxide precursor or a metal phosphate precursor, and wherein the liquid is a hydrocarbon, water, or an alcohol.

5. The method as defined in claim 1 wherein the carbon precursor is one of the aromatic functional groups containing silanes which are selected from the group consisting of Diphenylsilanediol, Diphenylsilane, Triethoxy(l-phenylethenyl)silane, Trimethyl(phenoxy)silane, Trimethyl(phenyl)silane, Diphenyl(silane-d 2 ), and Triphenyl(vinyl)silane).

6. The method as defined in claim 1 wherein the substrate is silicon or silicon having an oxide layer thereon, and wherein one of:

the aromatic hydrocarbons are selected from the group consisting of benzene, naphthalene, toluene, and xylene; or

the aromatic functional groups containing silanes are selected from the group consisting of Diphenylsilanediol, Diphenylsilane, Triethoxy(1-phenylethenyl)silane, Trimethyl(phenoxy)silane, Trimethyl(phenyl)silane, Diphenyl(silane-d 2 ), and Triphenyl(vinyl)silane).

7. The method as defined in claim 1 , further comprising creating at least one pore in the substrate.

8. The method as defined in claim 1 wherein the carbon layer is porous, and wherein the method further comprises selecting process conditions for the generating and the exposing that enable the porous carbon layer to be formed.

9. The method as defined in claim 1 wherein the carbon coating is a substantially graphitic carbon layer, and wherein the method further comprises selecting process conditions for the generating and the exposing that enable the substantially graphitic carbon layer to be formed.

10. The method as defined in claim 9 , further comprising depositing an artificial solid electrolyte interphase covering the substantially graphitic carbon layer.

11. A method for forming a lithium ion battery electrode material, the method comprising:

forming a substrate precursor solution including iron oleate and a carrier liquid;

exposing the substrate precursor solution to an atomization process, thereby generating aerosol droplets of the substrate precursor solution;

evaporating the carrier liquid from the aerosol droplets of the substrate precursor solution, thereby forming pre-substrate composite particles including carbon and nanocrystals of Fe and FeO x ; and

in the presence of a carbon precursor, heating the pre-substrate composite particles to at least a boiling point of the carbon precursor to evaporate the carbon precursor, thereby converting the pre-substrate composite particles to Fe 3 O 4 substrate particles and coating the Fe 3 O 4 substrate particles with a carbon layer.

12. The method as defined in claim 11 wherein the carbon precursor is diphenylsilanediol and wherein a silicate layer is formed between the Fe 3 O 4 substrate particles and the carbon layer during the heating step.

13. The method as defined in claim 1 wherein the substrate precursor is iron oleate.

14. The method as defined in claim 11 , further comprising creating at least one pore in the substrate.

15. The method as defined in claim 11 wherein the carbon layer is porous, and wherein the method further comprises selecting process conditions for the generating and the exposing that enable the porous carbon layer to be formed.

16. The method as defined in claim 11 wherein the carbon coating is a substantially graphitic carbon layer, and wherein the method further comprises selecting process conditions for the generating and the exposing that enable the substantially graphitic carbon layer to be formed.

17. The method as defined in claim 16 , further comprising depositing an artificial solid electrolyte interphase covering the substantially graphitic carbon layer.