Method of manufacturing negative electrode for lithium secondary batteries

1. A method of manufacturing a negative electrode for lithium secondary batteries, comprising:

manufacturing a negative electrode by forming a negative electrode active material layer on a negative electrode current collector, wherein the forming of the negative electrode active material layer comprises coating the negative electrode current collector with a negative electrode active material, and first compressing the negative electrode active material on the surface of the negative electrode current collector to form the negative electrode active material layer;

manufacturing a pre-lithiated negative electrode by impregnating the negative electrode with a pre-lithiation solution to perform a pre-lithiation process; and

second compressing the pre-lithiated negative electrode to adjust a porosity of the pre-lithiated negative electrode,

wherein the negative electrode active material comprises a silicon-based negative electrode active material and a carbon-based negative electrode active material,

wherein a weight ratio of the silicon-based negative electrode active material to the carbon-based negative electrode active material is 1:99 to 50:50,

wherein the porosity of the pre-lithiated negative electrode is in a range of 20% to 45%,

wherein the porosity is calculated by the following Equation 1:

Porosity (%)=[1−(Real Density/True Density)]×100  Equation 1

wherein real density is a density of the negative electrode active material layer comprising pores, and

true density is a solids density of the negative electrode active material layer without pores.

2. The method of claim 1 , wherein the porosity of the pre-lithiated negative electrode is in a range of 25% to 35%.

3. The method of claim 1 , wherein the pre-lithiation process comprises electrochemically charging the negative electrode using a lithium metal as a counter electrode after the negative electrode is impregnated with the pre-lithiation solution.

4. The method of claim 1 , wherein the impregnation is performed at a temperature of 10° C. to 200° C. for 2 hours to 48 hours.

5. The method of claim 3 , wherein the charging is performed to 5% to 35% of a charge capacity of the negative electrode at a current density of 0.1 mA/cm 2 to 10 mA/cm 2 .

6. The method of claim 1 , wherein the compression is performed at a linear pressure of 0.1 kN/cm to 30 kN/cm.

7. The method of claim 1 , wherein the pre-lithiation solution comprises a lithium salt and an organic solvent.

8. The method of claim 1 , wherein manufacturing of the pre-lithiated negative electrode comprises:

impregnating the negative electrode with the pre-lithiation solution to perform a pre-lithiation process; and

washing the negative electrode with an organic solvent.

9. The method of claim 8 , wherein washing is performed at a temperature of 10° C. to 200° C. for 1 minute to 3 hours using the organic solvent.

10. A method of manufacturing a lithium secondary battery comprising:

manufacturing a negative electrode as defined in claim 1 ;

manufacturing a positive electrode;

placing a separator between the negative electrode and the positive electrode; and

injecting an electrolyte solution into the lithium secondary battery.

11. The method of claim 1 , wherein the method consists of the steps of manufacturing the negative electrode, first compressing the negative electrode active material, manufacturing the pre-lithiated negative electrode, and second compressing the pre-lithiated negative electrode.

12. The method of claim 1 , wherein the step of first compressing the negative electrode active material and the step of second compressing the pre-lithiated negative electrode are performed before and after the step of manufacturing the pre-lithiated negative electrode, respectively.

13. The method of claim 1 , wherein the pre-lithiation solution comprises LiPF 6 dissolved to a concentration of 1 M in a solvent comprising ethylene carbonate (EC) and ethyl methyl carbonate (EMC) mixed at a volume ratio of 3:7 and 2% by weight of fluoroethylene carbonate (FEC).