FUNCTIONAL CONDUCTIVE MATERIAL, POSITIVE ELECTRODE COMPOSITE INCLUDING SAME, METHOD FOR MANUFACTURING SAME, AND LITHIUM SECONDARY BATTERY INCLUDING SAME

Abstract

A method for manufacturing a functional conductive material according to the present invention includes: preparing g a conductive material; reducing the conductive material; and oxidizing the reduced conductive material, in which the conductive material is sequentially reduced and oxidized so that an oxygen functional group is formed on a surface of the conductive material.

Claims

1. A method for manufacturing a functional conductive material, the method comprising: preparing a conductive material; reducing the conductive material; and oxidizing the reduced conductive material, wherein the conductive material is sequentially reduced and oxidized so that an oxygen functional group is formed on a surface of the conductive material.

2. The method of claim 1, wherein in the reducing of the conductive material, the conductive material is heat-treated in an inert gas atmosphere.

3. The method of claim 2, wherein at least any one of a carbonyl functional group, a sulfate functional group, a nitrate functional group, or an aldehyde functional group is removed from the surface of the conductive material by the reduction.

4. The method of claim 3, wherein a ratio (D/G) of a D peak (1, 350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the conductive material, to a G peak (1,582 (cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, is increased by the reduction, and the D peak and the G peak are observed in Raman analysis of the reduced conductive material.

5. The method of claim 2, wherein a reduction heat treatment temperature of the conductive material is 200 C. to 1,200 C., and a reduction heat treatment time of the conductive material is 1 hour to 8 hours.

6. The method of claim 1, wherein in the oxidizing of the reduced conductive material, the reduced conductive material is heat-treated in an air atmosphere.

7. The method of claim 6, wherein a ratio (D/G) of a D peak (1, 350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the conductive material, to a G peak (1,582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, is increased by the oxidation, as compared to the reduced conductive material, and the D peak and the G peak are sequentially observed in Raman analysis of the reduced and oxidized conductive material.

8. The method of claim 6, wherein an oxidation heat treatment temperature of the reduced conductive material is 25 C. to 500 C., and an oxidation heat treatment time of the reduced conductive material is 30 minutes to 5 hours.

9. A method for manufacturing a positive electrode composite, the method comprising: preparing the functional conductive material of claim 1 and a positive electrode active material; and physically mixing the functional conductive material and the positive electrode active material to manufacture the positive electrode composite.

10. The method of claim 9, wherein in the physically mixing of the functional conductive material and the positive electrode active material to manufacture the positive electrode composite, an electrolyte is further provided before physically mixing the functional conductive material and the positive electrode active material, the electrolyte includes a solid electrolyte, and the solid electrolyte includes a sulfide.

11. A positive electrode composite comprising: a positive electrode active material; and a functional conductive material provided on a surface of the positive electrode active material, wherein the functional conductive material includes a carbon structure and an oxygen functional group provided on a surface of the carbon structure.

12. The positive electrode composite of claim 11, wherein in Raman analysis on the functional conductive material, a ratio (D/G) of a D peak (1,350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the functional conductive material, to a G peak (1,582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, is equal to or greater than 0.323.

13. The positive electrode composite of claim 11, wherein the functional conductive material has oxygen atoms in a proportion of 0.74% or greater in XPS analysis on the functional conductive material.

14. The positive electrode composite of claim 11, further comprising an electrolyte provided on the surface of the positive electrode active material to surround the positive electrode active material and the functional conductive material, wherein the electrolyte includes a sulfide-based solid electrolyte.

15. A positive electrode composite comprising: a positive electrode active material; and a functional conductive material provided on a surface of the positive electrode active material, wherein the functional conductive material includes a carbon structure and an oxygen functional group provided on a surface of the carbon structure, and wherein a ratio (D/G) of a D peak (1,350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the functional conductive material, to a G peak (1,582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, is equal to or greater than 0.323 in Raman analysis on the functional conductive material.

16. A lithium secondary battery comprising: a positive electrode including the positive electrode composite of claim 11; a negative electrode disposed while being spaced apart from the positive electrode; and an electrolyte disposed between the positive electrode and the negative electrode, wherein a side reaction between the positive electrode and the electrolyte is decreased by the functional conductive material in which the oxygen functional group is provided on the surface of the positive electrode composite of the positive electrode, thereby improving charge/discharge capacity and rate characteristics.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0038] FIG. 1 is a flowchart for explaining a method for manufacturing a functional conductive material according to an embodiment of the present invention.

[0039] FIG. 2 is a view for explaining a conductive material according to the embodiment of the present invention.

[0040] FIG. 3 is a view for explaining a method for reducing the conductive material according to the embodiment of the present invention.

[0041] FIG. 4 is a view for explaining a method for oxidizing the reduced conductive material according to the embodiment of the present invention.

[0042] FIG. 5 is a flowchart for explaining a method for manufacturing a positive electrode composite according to the embodiment of the present invention.

[0043] FIG. 6 is a view for explaining the functional conductive material, a positive electrode active material, and an electrolyte according to the embodiment of the present invention.

[0044] FIG. 7 is a view for explaining a method for manufacturing the positive electrode composite by mixing the functional conductive material, the positive electrode active material, and the electrolyte according to the embodiment of the present invention.

[0045] FIG. 8 is a view for explaining the positive electrode composite according to the embodiment of the present invention.

[0046] FIG. 9 is a view for explaining a lithium secondary battery in which the positive electrode composite is applied to a positive electrode according to the embodiment of the present invention.

[0047] FIGS. 10 and 11 are graphs for comparing chemical properties of the conductive material according to Experimental Example 1, Comparative Example 1, and Comparative Example 2 of the present invention.

[0048] FIGS. 12 to 14 are graphs for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 1, Comparative Example 1, Comparative Example 2, and Comparative Example 3 of the present invention.

[0049] FIG. 15 is a graph for comparing side reactions of the lithium secondary battery according to Experimental Example 2, Comparative Example 4, Comparative Example 5, and Comparative Example 6 of the present invention.

[0050] FIG. 16 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 3, Comparative Example 1-1 and Comparative Example 2-1 of the present invention.

[0051] FIG. 17 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 1, Experimental Example 1-1, and Experimental Example 1-2 of the present invention.

[0052] FIG. 18 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Examples 1-3 to 1-5 of the present invention.

DETAILED DESCRIPTION OF THE INVENTION

[0053] Hereinafter, preferred embodiments of the present invention will be described in detail with reference to the accompanying drawings. However, the present invention may be embodied in different forms and should not be construed as limited to the embodiments set forth herein. Rather, the embodiments are provided so that this disclosure will be thorough and complete, and will fully convey the scope of the present invention to those skilled in the art.

[0054] In the present specification, it will be understood that when an element is referred to as being on another element, it can be formed directly on the other element or intervening elements may be present. In the drawings, the thicknesses of layers and regions are exaggerated for clarity.

[0055] In addition, it will be also understood that although the terms first, second, third, etc. may be used herein to describe various elements, these elements should not be limited by these terms. These terms are only used to distinguish one element from another element. Thus, a first element in some embodiments may be termed a second element in other embodiments without departing from the teachings of the present invention. Embodiments explained and illustrated herein include their complementary counterparts. As used herein, the term and/or includes any and all combinations of one or more of the associated listed elements.

[0056] The singular expression also includes the plural meaning as long as it does not differently mean in the context. In addition, the terms comprise, have etc., of the description are used to indicate that there are features, numbers, steps, elements, or combinations thereof, and they should not exclude the possibilities of combination or addition of one or more features, numbers, operations, elements, or a combination thereof. Furthermore, it will be understood that when an element is referred to as being connected or coupled to another element, it may be directly connected or coupled to the other element or intervening elements may be present.

[0057] In addition, when detailed descriptions of related known functions or constitutions are considered to unnecessarily cloud the gist of the present invention in describing the present invention below, the detailed descriptions will not be included.

[0058] FIG. 1 is a flowchart for explaining a method for manufacturing a functional conductive material according to an embodiment of the present invention, FIG. 2 is a view for explaining a conductive material according to the embodiment of the present invention, FIG. 3 is a view for explaining a method for reducing the conductive material according to the embodiment of the present invention, FIG. 4 is a view for explaining a method for oxidizing the reduced conductive material according to the embodiment of the present invention, FIG. 5 is a flowchart for explaining a method for manufacturing a positive electrode composite according to the embodiment of the present invention, FIG. 6 is a view for explaining the functional conductive material, a positive electrode active material, and an electrolyte according to the embodiment of the present invention, FIG. 7 is a view for explaining a method for manufacturing the positive electrode composite by mixing the functional conductive material, the positive electrode active material, and the electrolyte according to the embodiment of the present invention, FIG. 8 is a view for explaining the positive electrode composite according to the embodiment of the present invention, and FIG. 9 is a view for explaining a lithium secondary battery in which the positive electrode composite is applied to a positive electrode according to the embodiment of the present invention.

[0059] Referring to FIGS. 1 and 2, a conductive material 120 is prepared (S110).

[0060] The conductive material 120 may include a carbon structure. For example, the conductive material 120 may include a multi-walled carbon nanotube (MWCNT).

[0061] Referring to FIGS. 1 to 3, the conductive material 120 is reduced (S120).

[0062] The conductive material 120 may be heat-treated in an inert atmosphere by the reduction of the conductive material 120. For example, the inert atmosphere may be a mixed gas atmosphere in which hydrogen gas and argon gas are mixed. For example, a reduction heat treatment temperature of the conductive material 120 may be 200 C. to 1,200 C. In addition, a reduction heat treatment time of the conductive material 120 may be 1 hour to 8 hours. Accordingly, the conductive material 120 may be easily reduced to form a reduced conductive material 110. Therefore, an amount of carbon in the reduced conductive material 110 may be increased, and unnecessary functional groups may be removed. For example, the unnecessary functional groups may be carbonyl, sulfate, nitrate, and aldehyde.

[0063] In addition, a ratio (D/G) of a D peak (1,350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the reduced conductive material 110, to a G peak (1,582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, may be increased in Raman analysis on the reduced conductive material 110. For example, the D/G of the conductive material 120 may be 0.173. For example, the D/G of the reduced conductive material 110 may be 0.222.

[0064] Referring to FIGS. 1 and 4, the reduced conductive material 110 is oxidized (S130).

[0065] The reduced conductive material 110 may be heat-treated in an air atmosphere by the oxidation of the conductive material 110. For example, the air atmosphere may be an oxygen atmosphere. For example, an oxidation heat treatment temperature of the reduced conductive material 110 may be 25 C. to 500 C. In addition, an oxidation heat treatment time of the reduced conductive material 110 may be 30 minutes to 5 hours. Accordingly, the reduced conductive material 110 may be easily oxidized to form a functional conductive material 100. Therefore, an oxygen functional group may be formed on a surface of the functional conductive material 100. That is, the functional conductive material 100 may be manufactured by sequentially reducing and oxidizing the conductive material 120, and thus the oxygen functional group may be provided on the surface of the functional conductive material 100. In other words, an oxidation degree of the functional conductive material 100, which is manufactured by sequentially reducing and oxidizing the conductive material 120, may be increased.

[0066] In addition, the ratio (D/G) of the D peak (1, 350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the functional conductive material 100, to the G peak (1, 582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, may be increased in Raman analysis on the functional conductive material 100. For example, the D/G of the conductive material 120 may be 0.173. For example, the D/G of the reduced conductive material 110 may be 0.222. For example, the D/G of the functional conductive material 100 may be 0.323.

[0067] Accordingly, charge/discharge capacity, Coulombic efficiency, and rate characteristics of a lithium secondary battery to be described below may be improved by the oxygen functional group provided on the surface of the functional conductive material 100.

[0068] As a result, the method for manufacturing the functional conductive material 100 according to the embodiment of the present application may include a step of preparing the conductive material 120, a step of reducing the conductive material 120, and a step of oxidizing the reduced conductive material 110.

[0069] Accordingly, it is possible to manufacture the functional conductive material 100 having the oxygen functional group provided on the surface of the conductive material by sequentially reducing and oxidizing the conductive material 120. Therefore, a lithium secondary battery with improved charge/discharge capacity, Coulombic efficiency, and rate characteristics may be provided.

[0070] Referring to FIGS. 5 and 6, the functional conductive material 100 and a positive electrode active material 200 may be prepared (S410).

[0071] The functional conductive material 100 may include the carbon structure and the oxygen functional group provided on a surface of the carbon structure.

[0072] The positive electrode active material may include, for example, Ni, Mn, and Co. In addition, as a content Ni in the positive electrode active material increases, the oxidation degree of the functional conductive material 100 in a positive electrode composite 400 to be described below may increase. Accordingly, the charge/discharge capacity, the Coulombic efficiency, and the rate characteristics of the lithium secondary battery may be improved.

[0073] Referring to FIGS. 5 and 7, the functional conductive material 100 and the positive electrode active material 200 are physically mixed to manufacture the positive electrode composite 400 (S420).

[0074] In the step of physically mixing the functional conductive material 100 and the positive electrode active material 200 to manufacture the positive electrode composite 400, an electrolyte 300 may be further provided before physically mixing the functional conductive material 100 and the positive electrode active material 200.

[0075] The electrolyte 300 may include a solid electrolyte or a liquid electrolyte. For example, when the electrolyte 300 is the solid electrolyte, the solid electrolyte may include Li.sub.6PS.sub.5Cl.

[0076] Accordingly, the functional conductive material 100, the positive electrode active material 200, and the electrolyte 300 may be physically mixed to manufacture the positive electrode composite 400.

[0077] As a result, the method for manufacturing the positive electrode composite 400 according to the embodiment of the present application may include a step of preparing the functional conductive material 100, the positive electrode active material 200, and the electrolyte 300, and a step of physically mixing the functional conductive material 100, the positive electrode active material 200, and the electrode electrolyte 300 to manufacture the positive composite 400.

[0078] The positive electrode active material 200 may include Ni. Therefore, in the step of physically mixing the functional conductive material 100, the positive electrode active material 200, and the electrolyte 300 to manufacture the positive electrode composite 400, it is possible to control the oxidation degree of the functional conductive material 100 according to the content of Ni in the positive electrode active material 200. Accordingly, it is possible to manufacture the positive electrode composite 400 with the increased oxidation degree of the functional conductive material 100 by using the positive electrode active material 200 including a high content of Ni. Therefore, the lithium secondary battery with improved charge/discharge capacity, Coulombic efficiency, and rate characteristics may be provided.

[0079] Referring to FIG. 3, the positive electrode composite 400 will be described.

[0080] The positive electrode composite 400 may further include the electrolyte 300 provided on the positive electrode active material 200, the functional conductive material provided on the surface of the positive electrode active material 200, and the surface of the positive electrode active material 200 and surrounding the positive electrode active material 200 and the functional conductive material 100.

[0081] The functional conductive material 100 may include the carbon structure and the oxygen functional group provided on the surface of the carbon structure. For example, the carbon structure may be the MWCNT. In addition, the electrolyte 300 may be the solid d electrolyte. For example, when the electrolyte 300 may include Li.sub.6PS.sub.5Cl.

[0082] In addition, the ratio (D/G) of the D peak (1, 350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the functional conductive material 100, to the G peak (1,582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, may be equal to or greater than 0.323 in Raman analysis on the functional conductive material 100 of the positive electrode composite 400.

[0083] In addition, the functional conductive material 100 may have oxygen atoms in a proportion of 0.74% in XPS analysis on the functional conductive material 100 of the positive electrode composite 400.

[0084] Therefore, the lithium secondary battery with improved charge/discharge capacity, Coulombic efficiency, and rate characteristics may be provided by the oxygen functional group provided on the surface of the functional conductive material 100 of the positive electrode composite 400.

[0085] Referring to FIG. 9, a lithium secondary battery 700 in which the positive electrode composite 400 is applied to a positive electrode 500 will be described.

[0086] The lithium secondary battery 700 may include the positive electrode 500 including the positive electrode composite 400, a negative electrode 600 disposed while being spaced apart from the positive electrode 500; and the electrolyte 300 disposed between the positive electrode 500 and the negative electrode 600. For example, the negative electrode may include a lithium-indium alloy. For example, the electrolyte 300 may include a solid electrolyte or a liquid electrolyte. For example, when the electrolyte 300 is the solid electrolyte, the electrolyte 300 may include Li.sub.6PS.sub.5Cl.

[0087] A side reaction between the positive electrode 500 and the electrolyte 300 may be decreased by the functional conductive material 100 having the oxygen functional group provided in the positive electrode composite 400 of the positive electrode 500 of the lithium secondary battery 700. Therefore, the lithium secondary battery 700 with improved charge/discharge capacity, Coulombic efficiency, and rate characteristics may be provided.

[0088] Hereinafter, specific experimental examples and characteristic evaluation results of the conductive material, the positive electrode composite, and the lithium secondary battery according to the embodiment of the present invention will be described.

Conductive Material According to Experimental Example 1

[0089] As the conductive material, a multi-walled carbon nanotube (MWCNT, diameter: 20 nm to 30 nm, length: 5 um to 15 um) was prepared. The conductive material was heated to 900 C. (temperature increase rate: 5 C./min) in an inert atmosphere (hydrogen gas (5 wt %)+argon gas, hydrogen gas flow rate: 100 sccm), and reduced for 6 hours. The reduced conductive material was heated to 300 C. (temperature increase rate: 5 C./min) in an air atmosphere (air flow rate: 100 sccm), and oxidized for 2 hours to manufacture a functional conductive material (O-MWCNT) having an oxygen functional group provided on a surface thereof.

Conductive Material According to Experimental Example 1-1

[0090] A conductive material (O-MWCNT-0.5 hr) according to Experimental Example 1-1 was manufactured in the same manner as the method for manufacturing the conductive material according to Experimental Example 1, except that the reduced conductive material was heated to 300 C. (temperature increase rate: 5 C./min) in an air atmosphere (air flow rate: 100 sccm), and oxidized for 30 minutes.

Conductive Material According to Experimental Example 1-2

[0091] A conductive material (O-MWCNT-4 hr) according to Experimental Example 1-2 was manufactured in the same manner as the method for manufacturing the conductive material according to Experimental Example 1, except that the reduced conductive material was heated to 300 C. (temperature increase rate: 5 C./min) in an air atmosphere (air flow rate: 100 sccm), and oxidized for 4 minutes.

Conductive Material According to Comparative Example 1

[0092] As the conductive material, a multi-walled carbon nanotube (MWCNT, diameter: 20 nm to 30 nm, length: 5 um to 15 um) was prepared. The conductive material was heated to 900 C. (temperature increase rate: 5 C./min) in an inert atmosphere (hydrogen gas (5 wt %)+argon gas, hydrogen gas flow rate: 100 sccm), and reduced for 6 hours to manufacture a conductive material (R-MWCNT, Reduced-MWCNT) according to Comparative Example 1.

Conductive Material According to Comparative Example 2

[0093] As the conductive material according to Comparative Example 2, a multi-walled carbon nanotube (MWCNT, diameter: 20 nm to 30 nm, length: 5 um to 15 um) was prepared.

Conductive Material According to Comparative Example 3

[0094] As the conductive material according to Comparative Example 3, SUPER-C was prepared.

TABLE-US-00001 TABLE 1 Classification Conductive material Note Experimental O-MWCNT Reduction (6 h) .fwdarw. Example 1 Oxidation (2 h) Experimental O-MWCNT Reduction (6 h) .fwdarw. Example 1-1 Oxidation (0.5 h) Experimental O-MWCNT Reduction (6 h) .fwdarw. Example 1-2 Oxidation (4 h) Comparative R-MWCNT Reduction (6 h) Example 1 Comparative MWCNT Example 2 Comparative SUPER-C Example 3

Positive Electrode Composite According to Experimental Example 1

[0095] A conductive material (O-MWCNT) according to Experimental Example 1, a positive electrode active material (NCM powder (N86)), diameter: about 9 um), and a solid electrolyte (Li6PS5Cl powder, diameter: about 1 um) were prepared.

[0096] The positive electrode active material, the solid electrolyte, and the conductive material were provided to a Voltex Mixer so as to have a weight ratio of 85:14:1 and mixed the same to manufacture a positive electrode composite.

Positive Electrode Composite According to Experimental Example 1-1

[0097] A positive electrode composite according to Experimental Example 1-1 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that the positive electrode active material, the solid electrolyte, and the conductive material were provided to a Voltex Mixer so as to have a weight ratio of 70:29:1.

Positive Electrode Composite According to Experimental Example 1-2

[0098] A positive electrode composite according to Experimental Example 1-2 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that the positive electrode active material, the solid electrolyte, and the conductive material were provided to a Voltex Mixer so as to have a weight ratio of 70:28:2.

Positive Electrode Composite According to Experimental Example 1-3

[0099] A positive electrode composite according to Experimental Example 1-3 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that the conductive material according to Experimental Example 1-2 was prepared as the conductive material and Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 was prepared as the solid electrolyte.

Positive Electrode Composite According to Experimental Example 1-4

[0100] A positive electrode composite according to Experimental Example 1-4 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that the conductive material according to Experimental Example 1-3 was prepared as the conductive material and Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 was prepared as the solid electrolyte.

Positive Electrode Composite According to Experimental Example 1-5

[0101] A positive electrode composite according to Experimental Example 1-5 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 was prepared as the solid electrolyte.

Positive Electrode Composite According to Experimental Example 2

[0102] The conductive material (O-MWCNT) according to Experimental Example 1 and the solid electrolyte (Li.sub.6PS.sub.5Cl powder, diameter: about 1 um) were prepared.

[0103] The solid electrolyte and the conductive material were provided to a Voltex Mixer so as to have a weight ratio of 70:30 and mixed the same to manufacture a positive electrode composite.

Positive Electrode Composite According to Experimental Example 3

[0104] A positive electrode composite was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that NCM333 having a content of Ni that is lower than that of NCM powder (N86) was prepared as the positive electrode active material.

Positive Electrode Composite According to Comparative Example 1

[0105] A positive electrode composite (R-MWCNT) according to Comparative Example 1 was manufactured in the same manner as the method for manufacturing the positive electrode composite according Experimental Example 1, except that the conductive material (R-MWCNT) according to Comparative Example 1 was prepared as the conductive material.

Positive Electrode Composite According to Comparative Example 1-1

[0106] A positive electrode composite according to Comparative Example 1-1 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that NCM333 having a content of Ni that is lower than that of NCM powder (N86) was prepared as the positive electrode active material and the conductive material (R-MWCNT) according to Comparative Example 1 was prepared as the conductive material.

Positive Electrode Composite According to Comparative Example 2

[0107] A positive electrode composite (MWCNT) according to Comparative Example 2 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except the conductive material (MWCNT) according to Comparative Example 2 was prepared as the conductive material.

Positive Electrode Composite According to Comparative Example 2-1

[0108] A positive electrode composite according to Comparative Example 2-1 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that NCM333 having a content of Ni that is lower than that of NCM powder (N86) was prepared as the positive electrode active material and the conductive material (MWCNT) according to Comparative Example 2 was prepared as the conductive material.

Positive Electrode Composite According to Comparative Example 3

[0109] A positive electrode composite (Super-C) according to Comparative Example 3 was manufactured in the same manner as the method for manufacturing the positive electrode composite according to Experimental Example 1, except that the conductive material (Super-C) according to Comparative Example 3 was prepared as the conductive material.

TABLE-US-00002 TABLE 2 Weight ratio (wt %) of conductive Positive material:solid electrode electrolyte:positive Conductive Solid active electrode Classification material electrolyte material active material Experimental O-MWCNT Li.sub.6PS.sub.5Cl N86 85:14:1 Example 1 Experimental O-MWCNT Li.sub.6PS.sub.5Cl N86 70:29:1 Example 1-1 Experimental O-MWCNT Li.sub.6PS.sub.5Cl N86 70:28:2 Example 1-2 Experimental O-MWCNT Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 85:14:1 Example 1-3 (0.5 h) Experimental O-MWCNT Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 85:14:1 Example 1-4 (4 h) Experimental O-MWCNT Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 85:14:1 Example 1-5 (2 h) Experimental O-MWCNT Li.sub.6PS.sub.5Cl 70:30:0 Example 2 Experimental O-MWCNT Li.sub.6PS.sub.5Cl NCM333 85:14:1 Example 3 Comparative R-MWCNT Li.sub.6PS.sub.5Cl N86 85:14:1 Example 1 Comparative R-MWCNT Li.sub.6PS.sub.5Cl NCM333 85:14:1 Example 1-1 Comparative MWCNT Li.sub.6PS.sub.5Cl N86 85:14:1 Example 2 Comparative MWCNT Li.sub.6PS.sub.5Cl NCM333 85:14:1 Example 2-1 Comparative SUPER-C Li.sub.6PS.sub.5Cl N86 85:14:1 Example 3

Lithium Secondary Battery According to Experimental Example 1

[0110] A solid electrolyte (Li.sub.6PS.sub.5Cl powder, diameter: about 1 um, 100 mg) was compressed at 125 MPa to manufacture an electrolyte. The positive electrode composite (9 mg) according to Experimental Example 1 was compressed at 200 MPa on an upper surface of the electrolyte to manufacture a positive electrode. In addition, a lithium-indium alloy was disposed on a lower surface of the electrolyte to manufacture a negative electrode, thereby manufacturing a lithium secondary battery.

Lithium Secondary Battery to Experimental Example 1-1

[0111] A lithium secondary according to Experimental Example 1-1 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode composite according to Experimental Example 1-1 was compressed on the upper surface of the electrolyte to manufacture the positive electrode.

Lithium Secondary Battery According to Experimental Example 1-2

[0112] A lithium secondary according to Experimental Example 1-2 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode composite according to Experimental Example 1-2 was compressed on the upper surface of the electrolyte to manufacture the positive electrode.

Lithium Secondary Battery According to Experimental Example 1-3

[0113] A lithium secondary according to Experimental Example 1-3 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 serving as the solid electrolyte was compressed to manufacture the electrolyte and the positive electrode composite according to Experimental Example 1-3 was compressed on the upper surface of the electrolyte to manufacture the positive electrode.

Lithium Secondary Battery According to Experimental Example 1-4

[0114] A lithium secondary according to Experimental Example 1-4 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 serving as the solid electrolyte was compressed to manufacture the electrolyte and the positive electrode composite according to Experimental Example 1-4 was compressed on the upper surface of the electrolyte to manufacture the positive electrode.

Lithium Secondary Battery According to Experimental Example 1-5

[0115] A lithium secondary according to Experimental Example 1-5 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 serving as the solid electrolyte was compressed to manufacture the electrolyte and the positive electrode composite according to Experimental Example 1-5 was compressed on the upper surface of the electrolyte to manufacture the positive electrode.

Lithium Secondary Battery According to Experimental Example 2

[0116] A lithium secondary was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Experimental Example 2 and the negative electrode was manufactured by disposing a lithium metal on a lower surface of the electrolyte.

Lithium Secondary Battery According to Experimental Example 3

[0117] A lithium secondary according to Experimental Example 3 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite according to Experimental Example 3.

Lithium Secondary Battery According to Comparative Example 1

[0118] A lithium secondary was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Comparative Example 1.

Lithium Secondary Battery According to Comparative Example 1-1

[0119] A lithium secondary according to Comparative Example 1-1 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Composite According to Comparative Example 1-1.

Lithium Secondary Battery According to Comparative Example 2

[0120] A lithium secondary according to Comparative Example 2 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite according to Comparative Example 2.

Lithium Secondary Battery According to Comparative Example 2-1

[0121] A lithium secondary according to Comparative Example 2-1 was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Composite According to Comparative Example 2-1.

Lithium Secondary Battery According to Comparative Example

[0122] A lithium secondary according to Comparative Example 3 was manufactured in the same manner s the method for manufacturing the lithium secondary battery according to Experimental Example 1, except that the positive electrode was manufactured on the upper surface of the electrolyte using the e positive electrode composite according to Comparative Example 3.

Lithium Secondary Battery According to Comparative Example 4

[0123] A lithium secondary was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 2, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Comparative Example 1.

Lithium Secondary Battery According to Comparative Example 5

[0124] A lithium secondary was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 2, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Comparative Example 2.

Lithium Secondary Battery According to Comparative Example 6

[0125] A lithium secondary was manufactured in the same manner as the method for manufacturing the lithium secondary battery according to Experimental Example 2, except that the positive electrode was manufactured on the upper surface of the electrolyte using the positive electrode composite (9 mg) according to Comparative Example 3.

TABLE-US-00003 TABLE 3 Positive electrode (positive electrode composite) Positive electrode Negative active Solid Conductive Classification electrode Electrolyte material electrolyte material Experimental Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl O-MWCNT Example 1 indium (85 wt %) (14 wt %) (1 wt %) alloy Experimental Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl O-MWCNT Example 1-1 indium (70 wt %) (29 wt %) (1 wt %) alloy Experimental Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl O-MWCNT Example 1-2 indium (70 wt %) (28 wt %) (2 wt %) alloy Experimental Lithium- Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 O-MWCNT Example 1-3 indium (0.5 h) alloy Experimental Lithium- Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 O-MWCNT Example 1-4 indium (4 h) alloy Experimental Lithium- Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 N86 Li.sub.5.5PS.sub.4.5ClBr.sub.0.5 O-MWCNT Example 1-5 indium (2 h) alloy Experimental Lithium Li.sub.6PS.sub.5Cl Li.sub.6PS.sub.5Cl O-MWCNT Example 2 metal Experimental Lithium- Li.sub.6PS.sub.5Cl NCM333 Li.sub.6PS.sub.5Cl O-MWCNT Example 3 indium alloy Comparative Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl R-MWCNT Example 1 indium alloy Comparative Lithium- Li.sub.6PS.sub.5Cl NCM333 Li.sub.6PS.sub.5Cl R-MWCNT Example 1-1 indium alloy Comparative Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl MWCNT Example 2 indium alloy Comparative Lithium- Li.sub.6PS.sub.5Cl NCM333 Li.sub.6PS.sub.5Cl MWCNT Example 2-1 indium alloy Comparative Lithium- Li.sub.6PS.sub.5Cl N86 Li.sub.6PS.sub.5Cl SPUER-C Example 3 indium alloy Comparative Lithium Li.sub.6PS.sub.5Cl Li.sub.6PS.sub.5Cl R-MWCNT Example 4 metal Comparative Lithium Li.sub.6PS.sub.5Cl Li.sub.6PS.sub.5Cl MWCNT Example 5 metal Comparative Lithium Li.sub.6PS.sub.5Cl Li.sub.6PS.sub.5Cl SPUER-C Example 6 metal

[0126] FIGS. 10 and 11 are graphs for comparing chemical properties of the conductive material according to Experimental Example 1, Comparative Example 1, and Comparative Example 2 of the present invention.

[0127] Referring to FIG. 10, Raman analysis was performed on the conductive material (O-MWCNT) according to Experimental Example 1, the conductive material (R-MWCNT) according to Comparative Example 1, and the conductive material (R-MWCNT) according to Comparative Example 2. A ratio (D/G) of a D peak (1, 350 cm.sup.1), which corresponds to double resonance generated due to a disordered crystal structure of the conductive material (O-MWCNT) according to Experimental Example 1, the conductive material (R-MWCNT) according to Comparative Example 1, and the conductive material (R-MWCNT) according to Comparative Example 2, to a G peak (1, 582 cm.sup.1), which corresponds to planar vibration between carbon atoms in an aligned graphene sheet, may be calculated. Referring to FIG. 11, proportions (%) of oxygen atoms in the conductive material (O-MWCNT) according to Experimental Example 1, the conductive material (R-MWCNT) according to Comparative Example 1, and the conductive material (R-MWCNT) according to Comparative Example 2 were measured using XPS. In addition, results thereof are summarized in <Table 4> below.

[0128] As can be seen from FIG. 10, it can be seen that the D/G ratio of the conductive material according to Experimental Example 1 is the highest. The factor is interpreted as being due to the fact that the structure of the aligned graphene sheet is deformed by the oxygen functional group provided on the surface of the conductive material according to Experimental Example 1, and the ratio of the disordered structure is increased.

[0129] As can be seen from FIG. 11, it can be seen that the proportion of oxygen in the conductive material according to Experimental Example 1 is the highest. The factor is interpreted as being due to the fact that the conductive material is sequentially reduced and oxidized during manufacturing of the conductive material according to Experimental Example 1. Accordingly, it can be seen that the oxygen functional group is formed on the surface of the conductive material according to Experimental Example 1.

[0130] Therefore, it can be seen that in the method for manufacturing a functional conductive material according to the embodiment of the present invention, the method for reducing and oxidizing the conductive material is a method for forming an oxygen functional group (functional group) on the surface of the conductive material.

TABLE-US-00004 TABLE 4 Conductive D/G Proportion Classification material ratio of oxygen atoms Note Experimental O-MWCNT 0.323 0.74 Reduction .fwdarw. Example 1 Oxidation Comparative R-MWCNT 0.222 0.47 Reduction Example 1 Comparative MWCNT 0.173 0.59 Example 2

[0131] FIGS. 12 to 14 are graphs for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 1, Comparative Example 1, Comparative Example 2, and Comparative Example 3 of the present invention.

[0132] Referring to FIG. 12, charge/discharge capacities of the lithium secondary battery (O-MWCNT) according to Experimental Example 1, the lithium secondary battery (R-MWCNT) according to Comparative Example 1, the lithium secondary battery (MWCNT) according to Comparative Example 2, and the lithium secondary battery (SUPER-C) according to Comparative Example 3 were measured under the condition of 2.4 V to 3.7 V (vs. In). In addition, results thereof are summarized in <Table 5> below. Referring to FIG. 13, for the lithium secondary battery (O-MWCNT) according to Experimental Example 1, the lithium secondary battery (R-MWCNT) according to Comparative Example 1, the lithium secondary battery (MWCNT) according to Comparative Example 2, and the lithium secondary battery (SUPER-C) according to Comparative Example 3, Coulombic efficiency (C.E) and cycle retention (C.R) were measured under the conditions that one charge/discharge cycle was 0.05 C-rate and the remaining 99 charge/discharge cycles were 0.33 C-rate. In addition, results thereof are summarized in <Table 5> below. Referring to FIG. 14, rate characteristics of the lithium secondary battery (O-MWCNT) according to Experimental Example 1, the lithium secondary battery (R-MWCNT) according to Comparative Example 1, and the lithium secondary battery (MWCNT) according to Comparative Example 2 were evaluated for each charge/discharge rate (0.05 C-rate to 2 C-rate). In addition, results thereof are summarized in Table 6 below.

[0133] As can be seen from FIG. 12, it can be seen that the charge/discharge capacity of the lithium secondary battery according to Experimental Example 1 is the highest.

[0134] As can be seen from FIG. 13, it can be seen that the Coulombic efficiency and the cycle retention for the charge/discharge cycle of the lithium secondary battery according to Experimental Example 1 are the highest.

[0135] As can be seen from FIG. 14, it can be seen that the discharge capacity for each charge/discharge rate of the lithium secondary battery according to Experimental Example 1 is the highest, and the discharge cycle retention thereof is the highest. Accordingly, it can be seen that the rate characteristics of the lithium secondary battery according to Experimental Example 1 is best.

[0136] The factor is interpreted as being due to the oxygen functional group provided on the surface of the conductive material in the positive electrode of the lithium secondary battery according to Experimental Example 1. Therefore, it can be seen that the charge/discharge capacity, the Coulombic efficiency, the cycle retention, and the rate characteristics of the lithium secondary battery are improved.

TABLE-US-00005 TABLE 5 Charge Discharge Conductive capacity capacity C.E C.R Classification material (mAhg.sup.1) (mAhg.sup.1) (%) (%) Experimental O-MWCNT 245.12 194.36 79.29 61.42 Example 1 Comparative R-MWCNT 218.83 169.25 77.34 58.85 Example 1 Comparative MWCNT 219.89 172.30 78.37 51.26 Example 2 Comparative SUPER-C 218.45 169.40 77.55 48.65 Example 3

TABLE-US-00006 TABLE 6 Specific Capacity (mAhg.sup.1) Conductive 0.05 C- 0.1 C- 0.5 C- 1 C- 2 C- 2 C- Classification material rate rate rate rate rate rate Experimental O-MWCNT 189.77 182.69 148.57 112.07 49.87 177.95 Example 1 Comparative R-MWCNT 170.20 162.49 104.43 53.33 22.1 152.32 Example 1 Comparative MWCNT 175.16 168.96 114.21 68.73 17.25 161.02 Example 2

[0137] FIG. 15 is a graph for comparing side reactions of the lithium secondary battery according to Experimental Example 2, Comparative Example 4, Comparative Example 5, and Comparative Example 6 of the present invention.

[0138] Referring to FIG. 15, cyclic voltammetries (CVs) of the lithium secondary battery (O-MWCNT) according to Experimental Example 2, the lithium secondary battery (R-MWCNT) according to Comparative Example 4, the lithium secondary battery (MWCNT) according to Comparative Example 5, and the lithium secondary battery (SUPER-C) according to Comparative Example 6 were measured under the conditions of 3.0 V to 4.3 V (vs. Li/Lit) and 0.2 mV/s.

[0139] As can be seen from FIG. 15, it can be seen that the side reaction of the lithium secondary battery according to Experimental Example 2 is the smallest.

[0140] The factor is interpreted as being due to the fact that the side reaction between the positive electrode and the electrolyte is suppressed by the oxygen functional group provided on the surface of the conductive material of the positive electrode of the lithium secondary battery according to Experimental Example 2.

[0141] Therefore, it can be seen that the side reaction at an interface between the positive electrode and the electrolyte is suppressed by the oxygen functional group provided on the surface of the functional conductive material according to the embodiment of the present invention, thereby improving electrochemical properties of the lithium secondary battery.

[0142] FIG. 16 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 3, Comparative Example 1-1 and Comparative Example 2-1 of the present invention.

[0143] Referring to FIG. 16, charge/discharge capacities and Coulombic efficiency of the conductive material (O-MWCNT) according to Experimental Example 3, the conductive material (R-MWCNT) according to Comparative Example 1 1, and the conductive material (MWCNT) according to Comparative Example 2-1 were measured under the condition of 2.4 V to 3.7 V (vs. In).

[0144] As can be seen from FIG. 16, it can be seen that the charge/discharge capacity and the Coulombic efficiency of the lithium secondary battery according to Experimental Example 3 are the highest. The factor is interpreted as being due to the oxygen functional group provided on the surface of the conductive material in the positive electrode of the lithium secondary battery according to Experimental Example 3.

[0145] In addition, when comparing the result described in FIG. 16 with the result described in FIG. 12, it can be seen that the oxidation degree of the conductive material is controlled according to the type of the positive electrode active material. Specifically, it can be seen that the oxidation degree of the conductive material increases as the Ni content of the positive electrode active material increases.

[0146] FIG. 17 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Example 1, Experimental Example 1-1, and Experimental Example 1-2 of the present invention.

[0147] Referring to FIG. 17, charge/discharge capacities and Coulombic efficiency (C.E) of the conductive material (85:14:1) according to Experimental Example 1, the conductive material (70:29:1) according to Experimental Example 1 1, and the conductive material (70:28:2) according to Experimental Example 1-1 were measured under the condition of 2.4 V to 3.7 V (vs. In).

[0148] As can be seen from FIG. 17, it can be seen that the charge/discharge capacity and the Coulombic efficiency of the lithium secondary battery according to Experimental Example 1 are the highest.

[0149] Therefore, in the method for manufacturing the positive electrode composite according to the embodiment of the present application, it can be seen that the method for controlling the weight ratio of the positive electrode active material, the solid electrolyte, and the conductive material to be 85:14:1 is a method for improving the charge/discharge capacity and the Coulombic efficiency of the lithium secondary battery.

[0150] FIG. 18 is a table for comparing electrochemical properties of the lithium secondary battery according to Experimental Examples 1-3 to 1-5 of the present invention.

[0151] Referring to FIG. 18, charge/discharge capacities and Coulombic efficiency (C.E) of the conductive material (0-MWCNT-0. 5 hr-2 hr) according to Experimental Example 1-3, the conductive material (R-MWCNT) according to Comparative Example 1 1, and the conductive material (-MWCNT) according to Comparative Example 1-1 were measured under the condition of 2.4 V to 3.7 V (vs. In).

[0152] As can be seen from FIG. 18, it can be seen that the charge/discharge capacity and the Coulombic efficiency of the lithium secondary battery according to Experimental Example 1-4 are the highest.

[0153] Therefore, in the electrochemically unstable electrolyte (Li.sub.5.5PS.sub.4.5ClBr.sub.0.5), it can be seen that a higher oxidation degree of the conductive material is required as compared with the electrochemically stable electrolyte (Li.sub.6PS.sub.5Cl). In addition, in the method for increasing the oxidation degree of the conductive material, it can be seen that the method for increasing the oxidation time of the reduced conductive material is a method for increasing the oxidation degree of the conductive material.

[0154] While the present invention has been described in connection with the embodiments, it is not to be limited thereto but will be defined by the appended claims. In addition, it is to be understood that those skilled in the art may substitute, change, or modify the embodiments in various forms without departing from the scope and spirit of the present invention.