Si@C core/shell Nanomaterials for High Performance Anode of Lithium Ion Batteries

• US 20150162617A1
• Filed: 11/13/2014
• Published: 06/11/2015
• Est. Priority Date: 12/09/2013
• Status: Abandoned Application

• Current Assignee: Nano and Advanced Materials Institute Limited
• Original Assignee: Nano and Advanced Materials Institute Limited
• Inventors: LIU, Chenmin, CAI, Lifeng, CHOI, Shing Yan, WONG, Ka Kan
• Application Number:
  US14/541,111
• Publication Number:
  US 20150162617A1
• Time in Patent Office: Days
• US Class Current: 1/1
• CPC Class Codes: H01M 10/0525 Rocking-chair batteries, i.e. batteries with lithium insertion or intercalation in both electrodes; Lithium-ion batteries
• CPC Class Codes: H01M 2004/021 Physical characteristics, e.g. porosity, surface area
• CPC Class Codes: H01M 2004/027 Negative electrodes
• CPC Class Codes: H01M 4/0471 involving thermal treatment, e.g. firing, sintering, backing particulate active material, thermal decomposition, pyrolysis
• CPC Class Codes: H01M 4/134 Electrodes based on metals, Si or alloys
• CPC Class Codes: H01M 4/1395 of electrodes based on metals, Si or alloys
• CPC Class Codes: H01M 4/366 as layered products
• CPC Class Codes: H01M 4/386 Silicon or alloys based on silicon
• CPC Class Codes: H01M 4/583 Carbonaceous material, e.g. graphite-intercalation compounds or CFx
• CPC Class Codes: H01M 4/587 for inserting or intercalating light metals
• CPC Class Codes: H01M 4/625 Carbon or graphite
• CPC Class Codes: Y02E 60/10 Energy storage using batteries

Abstract

The present invention is to tackle the volume expansion problem of the Si anode materials in the application of lithium ion batteries. In the present invention, a simple and green hydrothermal method is use to form loosely packed Si@C core/shell structure. A carbon coating layer is formed on controllably aggregated silicon nanoparticles in a one-step procedure by the hydrothermal carbonization of a carbon-rich precursor.

Claims

1. A method for fabricating a silicon core/carbon shell material, comprising:

providing silicon particles;

providing a structure directing agent comprising alcoholic solvent and water;

mixing the silicon particles with the structure directing agent and a carbon source to form a reaction mixture, wherein the silicon particles are dispersed in the alcoholic solvent to form silicon particle aggregation droplets;

heating the reaction mixture by a hydrothermal process to form one or more silicon cores and one or more carbon shells, wherein each of the silicon cores comprises a plurality of silicon clusters formed from the silicon particle aggregation droplets, and is enclosed by the carbon shell; and

calcinating the silicon cores enclosed by the carbon shell by a calcination process for further carbonizing the carbon shells.

2. The method of claim 1, wherein the silicon particles comprises a size in a range of 20 to 200 nm.

3. The method of claim 1, wherein the alcoholic solvent is ethanol, methanol, propanol, or a combination thereof.

4. The method of claim 3, wherein the structure directing agent comprises a ratio of water to ethanol in a range of 40:

1 to 20;

1 by volume.

5. The method of claim 1, wherein the reaction mixture comprises a ratio of the silicon particles and the carbon source within a range of 1:

20 to 1;

1 by weight.

6. The method of claim 1, wherein the carbon source is selected from the group consisting of glucose, cyclodextrin, sucrose, and combinations thereof.

7. The method of claim 1, wherein the reaction mixture comprises 0.01-0.2 g/mL of the silicon particles, 0.02-0.1 g/mL of the alcoholic solvent, and 0.05-1.2 g/mL of the carbon source.

8. The method of claim 1, wherein the hydrothermal process is performed in an autoclave, and comprises a reaction temperature of 180-220°

C., a reaction pressure of 1.5-3 atm, a reaction time of 8-24 hr, and a pH of 4-11.

9. The method of claim 1, wherein the calcination process is performed under inert gas, and comprises a first calcination process performed with a first calcination temperature of 350-420°

C. and a first calcination period of 2-4 hr, and a second calcination process performed with a second calcination temperature of 750-850°

C. and a second calcination period of 2-5 hr.

10. An anode material for a lithium ion battery, comprising the silicon core/carbon shell material fabricated by the method of claim 1.

11. A silicon core/carbon shell structure, comprising:

a silicon core comprising a plurality of silicon clusters;

a carbon shell; and

a plurality of gaps;

wherein each of the silicon clusters is aggregated by a plurality of silicon particles;

wherein the carbon shell encloses the silicon core and is chemically bonded to the silicon core; and

wherein the gaps are present among the silicon clusters, and between the silicon core and the carbon shell.

12. The silicon core/carbon shell structure of claim 11, wherein the carbon shell comprises a diameter in a range of 50 to 500 nm.

13. The silicon core/carbon shell structure of claim 11, wherein the carbon shell comprises a thickness in a range of 10 to 100 nm.

14. An anode material for a lithium ion battery, comprising the silicon core/carbon shell structure of claim 11.