SILICON OXIDE COMPOSITE FOR LITHIUM SECONDARY BATTERY ANODE MATERIAL AND METHOD FOR MANUFACTURING SAME

Abstract

The present invention relates to a silicon oxide composite for a lithium secondary battery anode material and a method for manufacturing same and, more specifically, to a silicon oxide composite for a lithium secondary battery anode material and a method for manufacturing same, wherein the silicon oxide composite comprises a Si cluster and MgxSiOy(0≤x≤3, 0≤y≤5) formed on a peripheral portion of the Si cluster.

Claims

1. A silicon oxide composite for a lithium secondary battery anode material, comprising: a Si cluster; and magnesium silicate, which is indicated as Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4), formed on a peripheral portion of the Si cluster.

2. The silicon oxide composite of claim 1, wherein the Si cluster; and the Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4) formed on a peripheral portion of the Si cluster form a core-shell structure.

3. The silicon oxide composite of claim 1, wherein the domain size of the Si (220) by the Si cluster is 12 nm or less.

4. The silicon oxide composite of claim 1, wherein in X-ray diffraction pattern analysis, a peak belonging to a Si crystal appears in a range of a diffraction angle 28°<2θ<29°, and wherein a peak belonging to a MgSiO.sub.3 crystal appears in a range of a diffraction angle 30.5°<2θ<31.5°.

5. The silicon oxide composite of claim 1, wherein in XRD analysis, full width at half maximum (FWHM) of Si (111) by the Si cluster is in a range of a 0.7 (deg) to 1.5 (deg).

6. The silicon oxide composite of claim 1, wherein the silicon oxide composite comprises a Mg.sub.2SiO.sub.4 (foresterite) crystal, and the content of the Mg.sub.2SiO.sub.4 (foresterite) crystal is smaller than that of a MgSiO.sub.3 (enstatite) crystal.

7. The silicon oxide composite of claim 1, wherein the peak intensity ratio between the Mg.sub.2SiO.sub.4 (foresterite) crystal phase and the MgSiO.sub.3 (enstatite) crystal phase (I.sub.Mg2SiO4/I.sub.MgSiO3) is in a range of 0 to 0.5 or less.

8. The silicon oxide composite of claim 1, wherein the silicon oxide composite comprises Mg in a ratio of 2 to 15 parts by weight relative to 100 parts by weight of the total.

9. The silicon oxide composite of claim 1, wherein the silicon oxide composite comprises a carbon film on the surface.

10. The silicon oxide composite of claim 9, wherein an average thickness of the carbon film is may be in a range of 5 nm to 100 nm.

11. A method of manufacturing the silicon oxide composite for a secondary battery anode material according to claim 1, comprising: mixing silicon powder, silicon oxide (SiO.sub.x, 0.01<x<2) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture; evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium, respectively, reacting them, and then depositing the resultant to form a silicon oxide composite; cooling the formed silicon oxide composite; and milling the cooled silicon oxide composite.

12. The method of claim 11, further comprising a step of cladding a surface of the milled silicon oxide composite with carbon.

13. The method of claim 11, wherein in the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, the molar ratio of O/Si in the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture is in a range of 0.9 to 1.1.

14. The method of claim 11, wherein in the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, an average particle diameter and a specific surface area of the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to be included as raw materials are in a range of 10 nm to 100 μm and 5 m.sup.2/g to 500 m.sup.2/g, respectively.

15. The method of claim 11, wherein after the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, the method further comprises a step of subjecting the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture to heat treatment at 800° C. to 1,100° C. under normal pressure for 1 to 3 hours.

16. The method of claim 11, wherein in the step of evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium, respectively, reacting them, and then depositing the resultant to form an oxide composite, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and the metallic magnesium are evaporated in separate reactors, respectively, and are reacted in a gaseous state.

17. The method of claim 11, wherein in the step of evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and the metallic magnesium, respectively, reacting them, and then depositing the resultant to form an oxide composite, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture is evaporated at 1,000° C. to 1,600° C. under a pressure of 0.001 torr to 5 torr.

18. The method of claim 11, wherein in the step of evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium, respectively, reacting them, and then depositing the resultant to form an oxide composite, the metallic magnesium is evaporated at 700° C. to 1,000° C. under a pressure of 0.001 torr to 2 torr.

19. The method of claim 11, wherein in the step of cladding with carbon, the silicon oxide composite is reacted with one or more carbon precursors selected from the group consisting of methane, propane, butane, acetylene, benzene, and toluene at 600° C. to 1,200° C. in a gaseous state.

20. An anode for a lithium secondary battery provided with the silicon oxide composite for a secondary battery anode material according to claim 1.

21. A lithium secondary battery, which comprises the anode for a lithium secondary battery provided with a silicon oxide composite for a secondary battery anode material of claim 20.

22. The anode for a lithium secondary battery of claim 20, wherein when the battery is charged twice, the peak in the vicinity of 0.45 V in the dQ/dV curve is greater than that at 0.25 V.

23. The anode for a lithium secondary battery of claim 22, wherein after the battery is discharged twice, the XRD peak derived from Mg.sub.xSiO.sub.y does not appear.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0040] FIG. 1 shows the results of TEM-EDX analysis of cut specimen of a silicon oxide composite for a lithium secondary battery anode material prepared in an Example of the present disclosure.

[0041] FIGS. 2 to 8 show the results of XRD analysis of the silicon oxide composites for a lithium secondary battery anode material prepared in Examples and Comparative Examples of the present disclosure.

[0042] FIG. 9 shows the results of XPS analysis for the silicon oxide composites for a lithium secondary battery anode material prepared in Examples and Comparative Examples of the present disclosure.

[0043] FIG. 10 shows schematic diagrams of components for a cross-section of a silicon oxide composite for a lithium secondary battery anode material prepared in an Example and a Comparative Example of the present disclosure.

[0044] FIGS. 11 and 12 show the measurement results of the electrochemical properties of the battery including an anode material of an Example and Comparative Example 3 of the present disclosure.

[0045] FIG. 13 shows Ex-Situ XRD measurement results of electrodes after charge/discharge of the batteries including an anode material of an Example and a Comparative Example of the present disclosure.

[0046] FIG. 14 shows the XRD measurement results after 100 cycles of a silicon oxide composite for a lithium secondary battery anode material prepared in an Example and a Comparative Example of the present disclosure.

[0047] FIG. 15 shows the STEM measurement results of a silicon oxide composite for a lithium secondary battery anode material prepared in an Example and a Comparative Example of the present disclosure.

[0048] FIG. 16 shows the TEM, STEM-HAADF, and STEM-EDS measurement results before and after charge/discharge of a battery including an anode material of an embodiment and a Comparative Example of the present disclosure.

[0049] FIG. 17 shows the schematic diagrams showing a change in the structure of a battery, before and after charge/discharge, which includes an anode material of an Example and Comparative Example 3 of the present disclosure.

DESCRIPTION OF EXEMPLARY EMBODIMENTS

[0050] Hereinafter, the present disclosure will be described in more detail through embodiments. Since these embodiments are merely for illustrating the present disclosure, the scope of the present disclosure is not to be construed as being limited by these embodiments.

[0051] As used herein, an expression such as “comprising/including” should be understood as an open-ended term containing the possibility of including other Examples, unless otherwise specifically stated in the phrase or sentence in which the expression is included.

[0052] As used herein, “preferred” and “preferably” refer to embodiments of the present disclosure that may provide certain advantages under certain circumstances. However, other embodiments may also be preferred, under the same or other circumstances. Additionally, the mentioning of one or more preferred embodiments does not mean that other embodiments are not useful, and it is not intended to exclude other embodiments from the scope of the present disclosure.

[0053] Hereinafter, a silicon oxide composite for a lithium secondary battery anode material of the present disclosure will be described in detail.

[0054] The present disclosure provides a silicon oxide composite for a lithium secondary battery anode material, which includes a Si cluster; and magnesium silicate, which is indicated as Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4), formed on a peripheral portion of the Si cluster.

[0055] A cross-section of a silicon oxide composite for a lithium secondary battery anode material according to the present disclosure is shown in FIG. 1. As shown in FIG. 1, it can be seen that the silicon oxide composite for a lithium secondary battery anode material according to the present disclosure includes a cluster, in which the concentration of Si is non-uniformly aggregated inside the particles, and includes Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4) (i.e., magnesium silicate) in the peripheral portion of the Si cluster.

[0056] With regard to the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium are evaporated to react in a gaseous state. Therefore, when raw materials are dissolved at a high temperature and evaporated under reduced pressure in a solid solution state, and react in a gaseous state and are cooled, an interface can be formed between the Si cluster and Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4) on the periphery as a phase separation between the products proceeds.

[0057] Therefore, the silicon oxide composite for a lithium secondary battery anode material of the present disclosure can include a Si cluster and Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4), which is magnesium silicate formed on the peripheral portion of the Si cluster, which cannot be formed at all by the conventional technology where magnesium is doped after a silicon composite is formed.

[0058] In the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, the Si cluster and Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4), which is formed on the peripheral portion of the Si cluster, can form a core shell structure.

[0059] Additionally, in the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, the domain size of Si (220) in the Si cluster may be 12 nm or less.

[0060] Additionally, with regard to the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, in X-ray diffraction pattern analysis, a peak belonging to a Si crystal may appear in a range of a diffraction angle 28°<2θ<29°, and a peak belonging to a MgSiO.sub.3 crystal may appear in a range of a diffraction angle 30.5°<2θ<31.5°.

[0061] With regard to the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, in X-ray diffraction pattern analysis, a full width at half maximum (FWHM) of Si (111) by the Si cluster may be in a range of 0.7 (deg) to 1.5 (deg).

[0062] The silicon oxide composite for a lithium secondary battery anode material of the present disclosure may include a Mg.sub.2SiO.sub.4 (foresterite) crystal, and the content of the Mg.sub.2SiO.sub.4 (foresterite) crystal may be smaller than that of a MgSiO.sub.3 (enstatite) crystal. With regard to the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, the peak intensity ratio between the Mg.sub.2SiO.sub.4 (foresterite) crystal phase and the MgSiO.sub.3 (enstatite) crystal phase (i.e., I.sub.Mg2SiO4/I.sub.MgSiO3) may be in a range of 0 to 0.5 or less.

[0063] The silicon oxide composite for a lithium secondary battery anode material of the present disclosure may include Mg in a ratio of 2 to 15 parts by weight, and preferably 2 to 10 parts by weight relative to 100 parts by weight of the total.

[0064] The silicon oxide composite for a lithium secondary battery anode material of the present disclosure may include a carbon film on a surface thereof.

[0065] In the silicon oxide composite for a lithium secondary battery anode material of the present disclosure, an average thickness of the carbon film may be in a range of 5 nm to 100 nm.

[0066] Hereinafter, a method of manufacturing a silicon oxide composite for a lithium secondary battery anode material of the present disclosure will be described in detail.

[0067] The present disclosure provides a method of manufacturing a silicon oxide composite for a secondary battery anode material according to the present disclosure, which includes:

[0068] mixing silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture;

[0069] evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium, respectively, reacting them, and then depositing the resultant to form an oxide composite;

[0070] cooling the formed silicon oxide composite; and

[0071] milling the cooled silicon oxide composite.

[0072] The method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure may further include a step of cladding a surface of the milled silicon oxide composite with carbon.

[0073] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, the powder mixture may be mixed by a drying method and stirred.

[0074] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0.9<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, the molar ratio of O/Si in the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture may be in a range of 0.9 to 1.1. When the molar ratio of O/Si in the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture is 0.9 or less or 1.1 or above, the yield of the silicon oxide composite may be significantly low.

[0075] Additionally, the surface of the silicon powder may be oxidized. In the process of manufacturing the silicon powder, the surface may be oxidized by oxygen in the air. The oxygen content of the silicon powder is not limited. When the oxygen content is 50 wt % or less relative to the entire silicon powder, the O/Si molar ratio can be well adjusted, and when it is 30 wt % or less, the O/Si molar ratio can be better adjusted.

[0076] In the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture may include the oxidized silicon powder in an amount of 30 wt % or more, preferably 50 wt % or more, and more preferably 70 wt % or more, relative to the total amount of the raw material mixture.

[0077] In the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, it is possible to control the reaction rate and manufacture a product of uniform quality even when the raw materials are dry-mixed in a powder state by including SiO.sub.x as a raw material. When the content of the silicon oxide powder is 30 wt % or less, it is difficult to control the evaporation rate of silicon oxide according to the reaction time at the time of evaporating the raw material powder mixture under heating/reduced pressure to react with magnesium vapor, and thus, it is difficult to obtain uniform quality and the yield of the reaction product may be low. Additionally, there is a disadvantage in that a higher evaporation temperature is required to increase the evaporation rate of the raw material powder mixture.

[0078] Additionally, the average particle diameter and the specific surface area of the silicon powder, silicon oxide (SiO.sub.x, 0<x<1.1) powder, and silicon dioxide powder to be included as raw materials may be in a range of 10 nm to 100 μm and 5 m.sup.2/g to 500 m.sup.2/g, respectively.

[0079] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, after the step of mixing the silicon powder, silicon oxide (SiO.sub.x, 0<x<1.1) powder, and silicon dioxide powder to prepare a Si/SiO.sub.x/SiO.sub.2 raw material powder mixture, the method may further include a step of subjecting the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture to heat treatment. With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of subjecting the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture to heat treatment, the raw material powder mixture may be subjected to heat treatment at 800° C. to 1,100° C. at normal pressure for 1 to 3 hours to increase the composition uniformity of the raw material powder mixture.

[0080] The heat treatment is preferably performed in an inert gas (e.g., argon, nitrogen, helium, etc.) or reducing gas (e.g., hydrogen) atmosphere. In an oxidizing gas atmosphere, the silicon powder and the silicon oxide powder may be oxidized, thereby reducing the yield.

[0081] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of evaporating the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium, respectively, reacting them, and then depositing the resultant to form an oxide composite, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and the metallic magnesium may be evaporated in separate reactors, respectively, and reacted in a gaseous state. The method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure may be performed such that the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and the metallic magnesium are evaporated in separate reactors by heating, and then reacted in a gaseous state, whereby the silicon oxide composite for a secondary battery anode material may be formed in a structure which includes a Si cluster; and magnesium silicate, which is indicated as Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4), formed on a peripheral portion of the Si cluster.

[0082] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, the evaporation of Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium may be performed at 800° C. to 1,600° C. under normal pressure under a pressure of 0.001 torr to 2 torr.

[0083] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of evaporating and depositing the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium to form an oxide composite, the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture may be performed at 1,000° C. to 1,600° C. under normal pressure under a pressure of 0.001 torr to 2 torr.

[0084] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of evaporating and depositing the Si/SiO.sub.x/SiO.sub.2 raw material powder mixture and metallic magnesium to form an oxide composite, the metallic magnesium may be performed at 800° C. to 1,000° C. under normal pressure under a pressure of 0.001 torr to 2 torr.

[0085] With regard to the method of manufacturing a silicon oxide composite for a secondary battery anode material of the present disclosure, in the step of cladding the surface with carbon, the silicon oxide composite may be reacted with one or more carbon precursors selected from the group consisting of methane, propane, butane, acetylene, benzene, and toluene at 600° C. to 1,200° C. in a gaseous state.

[0086] The present disclosure also provides an anode for a lithium secondary battery provided with a silicon oxide composite for a secondary battery anode material.

[0087] The present disclosure also provides a lithium secondary battery, which includes the anode for a lithium secondary battery provided with a silicon oxide composite for a secondary battery anode material according to the present disclosure.

[0088] In the lithium secondary battery of the present disclosure which includes the anode for a lithium secondary battery provided with a silicon oxide composite for a secondary battery anode material, when the battery is charged twice, the peak in the vicinity of 0.45 V in the dQ/dV curve may appear to be greater than that at 0.25 V.

[0089] In the lithium secondary battery which includes the anode for a lithium secondary battery, after the battery is discharged twice, the XRD peak derived from Mg.sub.xSiO.sub.y may not appear.

[0090] Hereinafter, the present disclosure will be described in detail by embodiments, but the present disclosure is not limited by these embodiments.

EXAMPLES

<Example 1> Preparation of Silicon Oxide Composite-Carbon Complex Powder Mg.SUB.8.—SiO.SUB.x./C

[0091] 20 kg of silicon powder with an average particle size of 20 μm, 50 kg of silicon dioxide powder with an average particle size of 20 nm, and 130 kg of silicon oxide (SiO.sub.x, x=1.03) powder with an average particle size of 200 μm were uniformly mixed by stirring with a Henschel mixer for 2 hours to form a raw material powder mixture. The raw material powder mixture was heat-treated at 1,000° C. at normal pressure under argon atmosphere for 2 hours.

[0092] The heat-treated raw material powder mixture and metallic magnesium in an amount of 16 kg were each added into furnace-A and furnace-B of a vacuum reactor, and the pressure was reduced to reach 0.1 torr, and heated. Then, the furnace-A including the raw material powder mixture was heated to 1,450° C. and the raw material powder mixture was evaporated, and metallic magnesium in the furnace-B was evaporated by raising the temperature to 850° C., and then reacted in a vapor state for 5 hours. A silicon oxide composite mass deposited on the substrate inside the reactor by reacting in a high-temperature gas phase was rapidly cooled to room temperature by a water-cooled substrate.

[0093] The silicon oxide composite mass was pulverized by a mechanical method to control the particle size so that the average particle size was 6 μm.

[0094] The pulverized silicon oxide composite powder (50 g) was added into a tube-type electric furnace and maintained it at 1,000° C. for 1 hour while flowing Ar gas and methane gas at 1 L/min each, to thereby prepare a silicon oxide composite-carbon complex powder Mgs-SiO.sub.x/C, whose surface was coated with carbon.

[0095] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Example 1, the content of Mg was measured to be 8 wt %.

<Example 2> Preparation of Silicon Oxide Composite-Carbon Complex Powder Mg.SUB.6.—SiO.SUB.x./C

[0096] A silicon oxide composite-carbon complex powder Mg.sub.6—SiO.sub.x/C was prepared in the same manner as in Example 1 except that 12 kg of the metallic magnesium of Example 1 was added.

[0097] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Example 2, the content of Mg was measured to be 6 wt %.

<Example 3> Preparation of Silicon Oxide Composite-Carbon Complex Powder Mg.SUB.3.—SiO.SUB.x./C

[0098] A silicon oxide composite-carbon complex powder Mg.sub.3—SiO.sub.x/C was prepared in the same manner as in Example 1 except that 6 kg of the metallic magnesium of Example 1 was added.

[0099] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Example 3, the content of Mg was measured to be 3 wt %.

<Example 4> Preparation of Silicon Oxide Composite-Carbon Complex Powder Mg.SUB.12.—SiO/C

[0100] A silicon oxide composite-carbon complex powder Mg.sub.12—SiO.sub.x/C was prepared in the same manner as in Example 1 except that 24 kg of the metallic magnesium of Example 1 was added.

[0101] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Example 4, the content of Mg was measured to be 12 wt %.

<Comparative Example 1> Preparation of Silicon Oxide Composite-Carbon Complex Powder

[0102] 20 kg of silicon powder with an average particle size of 20 μm and 50 kg of silicon dioxide powder with an average particle size of 20 nm were added into water, uniformly mixed by stirring for 12 hours, and dried at 1,200° C. (or 200° C.: temperature confirmation required) to form a raw material powder mixture.

[0103] The raw material powder mixture and metallic magnesium in an amount of 11 kg were each added into furnace-A and furnace-B of a vacuum reactor, and the pressure was reduced to reach 0.1 torr, and heated. Then, the furnace-A including the raw material powder mixture was heated to 1,600° C. and the raw material powder mixture was evaporated, and metallic magnesium in the furnace-B including was evaporated by raising the temperature to 900° C., and the vapor in the furnace-A and the vapor in the furnace-B were reacted for 3 hours. Then, silicon oxide composite-carbon complex powder of Comparative Example 1 was prepared by the process of the cooling, milling, and carbon cladding process as in Example 1.

[0104] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Comparative Example 1, the content of Mg was measured to be 13 wt %.

<Comparative Example 2> Preparation of Silicon Oxide Composite-Carbon Complex Powder

[0105] A silicon oxide composite-carbon complex powder of Comparative Example 2 was prepared in the same manner as in Comparative Example 1 except that 13 kg of the metallic magnesium of Comparative Example 1 was added.

[0106] As a result of ICP-MS analysis to measure the content of Mg in the silicon oxide composite-carbon complex powder prepared in Comparative Example 2, the content of Mg was measured to be 16 wt %.

<Comparative Example 3> Preparation of Silicon Oxide-Carbon Complex Powder SiO.SUB.x./C

[0107] 20 kg of silicon powder with an average particle size of 20 μm and 50 kg of silicon dioxide powder with an average particle size of 20 nm were added into water, uniformly mixed by stirring for 12 hours, and dried at 1,200° C. (or 200° C.: temperature confirmation required) to form a raw material powder mixture.

[0108] The raw material powder mixture was added into furnace-A and furnace-B, and the pressure was reduced to reach 0.1 torr, and heated. Then, the furnace-A including the raw material powder mixture was heated to 1,600° C. and deposited on a cooling plate for 3 hours. Then, the silicon oxide-carbon complex powder of Comparative Example 3 (i.e., SiO.sub.x/C), in which magnesium was not added, was prepared by the process of the cooling, milling, and carbon cladding process as in Example 1.

<Experimental Example> Measurement of TEM-EDX

[0109] With regard to the silicon oxide composite-carbon complex powder Mgs-SiO.sub.x/C sample for measurement prepared in Example 1 above, a processed surface (cross-section) was prepared through FIB processing by using FIB from the surface (a porous layer surface) of the sample for measurement to a depth direction (a direction toward the inside of the sample for measurement).

[0110] The obtained processed surface was subjected to TEM-EDX measurement (a reflected electron image) at an acceleration voltage of 2.1 kV and a magnification of 6,500, and the results are shown in FIG. 1.

[0111] As shown in FIG. 1, it was possible to confirm that the silicon oxide composite-carbon complex powder Mgs-SiO.sub.x/C prepared in Example 1 includes a Si cluster; and magnesium silicate indicated by Mg.sub.xSiO.sub.y (0.5≤x≤2, 2.5≤y≤4) formed on the peripheral portion of the Si cluster.

[0112] When the materials prepared in Examples 2 to 4 were subjected to TEM-EDX measurement in the same manner, it was confirmed that the measurement of the silicon oxide composite-carbon complex powder prepared in Examples 2 to 4 also included a Si cluster; and magnesium silicate formed on the peripheral portion of the Si cluster.

<Experimental Example> XRD Measurement

[0113] XRD data was measured for the materials prepared in Examples 1 to 4 and Comparative Examples 1 to 3 above. The results are shown in FIGS. 2 to 8, and the intensity at each peak was measured and shown in Table 1 below.

TABLE-US-00001 TABLE 1 Example Comparative Example 1 2 3 4 1 2 3 Mg Content 8 6 3 12 13 16 0 Si (111) 28.38 28.70 28.52 28.45 28.47 28.56 28.53 2θ (°) Si (111) 0.95 0.98 0.84 0.94 0.54 0.58 1.89 FWHM I.sub.MgSiO3(610)/ 0.14 0.21 0.26 0.20 0.11 0.19 — I.sub.Si (111) I.sub.Mg2SiO4/ 0 0 0 280.84/766.96 = 0.016/0.007 = 122.94/153.58 = I.sub.MgSiO3 0.366 2.29 0.8 Si c.s. 8.6 8.4 9.8 8.7 15.2 14.1 6 Domain Size

[0114] In FIG. 8, which shows the XRD measurement results for Comparative Example 3 material not doped with magnesium, it was confirmed that a peak by non-crystalline silicon oxide (a-SiO.sub.2) appeared in a range of 20° to 40°, and the peak by crystalline silicon oxide appeared with the highest intensity at 280 and 45°.

[0115] As shown in FIG. 2, it was observed that while only the peak due to the MgSiO.sub.3 crystal phase appeared in the case of Example 1, a peak due to the forsterite crystal phase of Mg.sub.2SiO.sub.4 appeared in the cases of Comparative Examples 1 and 2. Accordingly, it was confirmed that in the case of Examples that the peak intensity of the forsterite crystal phase of Mg.sub.2SiO.sub.4 at 32.5° and the peak intensity ratio I.sub.Mg2SiO4/I.sub.MgSiO3 of the MgSiO.sub.3 crystal phase were 0.5 or less.

<Experimental Example> Measurement of Domain Size

[0116] From the results of XRD measurement, the Si crystal size in the silicon oxide composite can be measured as follows.

[0117] Based on the full width at half maximum (FWHM) of the peak belonging to Si (111) in the X-ray diffraction pattern, the domain size was measured by the Sherrer equation expressed by the following General Formula 1(1), and the results are shown in Table 1 above.

C.S. [nm]=K˜λ/B.Math.cos θ  General Formula 1

[0118] In General Formula 1, K=0.9, λ=0.154 nm, B=FWHM (rad),

[0119] and θ=peak position (angle).

[0120] From Table 1 above, it was confirmed that the domain size of the crystalline silicon particles Si (220) increased in proportion to the content of Mg in the particles.

<Experimental Example> XPS Measurement

[0121] XPS of the particles prepared in Example and Comparative Example 3 was measured, and the results are shown in FIG. 9.

[0122] As shown in FIG. 9, it was confirmed that according to Example of the present disclosure, when the Mg content in the particles was 8 wt %, the peak by Mg.sub.2SiO.sub.4 did not appear but the peak by MgSiO.sub.3 appeared; however, according to Comparative Example of the present disclosure, when the Mg content in the particles was 13 wt %, the peak by Mg.sub.2SiO.sub.4 appeared.

[0123] Additionally, as shown in FIG. 9, it was confirmed that as the content of Mg in the particles increased, the peak intensity of Si0 (corresponding to a binding energy of 98 eV to 99 eV) and Si.sup.3+ (corresponding to Mg.sub.xSiO.sub.y) increased.

[0124] This confirms that as the Mg content in the particles increases, the reaction from SiO.sub.x to Si decreases, and Mg is converted into Mg.sub.xSiO.sub.y.

<Experimental Example> STEM-EDX Measurement

[0125] STEM-EDX of the particles prepared in Example was measured and the results are shown in FIG. 15. In FIG. 15, it can be seen that the shape of the silicon oxide composite prepared is cladded with a carbon layer of several tens of nm having a shape such as carbon nanofibers and graphene on the surface. In addition, it was confirmed in FIG. 15 that magnesium was uniformly distributed inside the silicon oxide composite powder prepared by the present disclosure.

<Preparation Example> Manufacture of Lithium Secondary Battery to which Silicon Oxide Composite is Applied

[0126] The silicon oxide composite powder prepared according to Examples 1 and 2 and Comparative Example 3 and natural graphite were mixed in a weight ratio of 73:27 so as to prepare an anode and a battery (coin cell) for a lithium secondary battery as an electrode active material.

[0127] The mixed active material, binder carboxy methyl cellulose (CMC), and styrene butadiene rubber (SBR) in a weight ratio of 97:1.5:1.5 were mixed with water to prepare an anode slurry.

[0128] An electrode with a thickness of 70 μm was prepared by coating the composition on a copper foil with a thickness of 18 μm followed by drying. An anode for a coin cell was prepared by punching the electrode-coated copper foil in a circular form with a diameter of 14 mm. A metallic lithium foil with a thickness of 0.3 mm was used as an opposite electrode.

[0129] A porous polyethylene sheet with a thickness of 0.1 mm was used as a separator. The electrolyte was prepared by dissolving 1 M LiPF.sub.6 in a solution where ethylene carbonate (EC) and diethylene carbonate (DEC) were mixed in a 1:1 volume ratio. A coin cell (battery) with a thickness of 2 mm and a diameter of 32 mm (so-called “2032 type”) was prepared by applying the constitutional elements above.

<Experimental Example> Evaluation of Electrochemical Characteristics

[0130] Each of the coin cells, which were prepared per sample in Preparation Example above, were charged with a static current of 0.1 C until the voltage reached 0.005 V, and then the coin cells were discharged with a static current 0.1 C until the voltage reached 2.0 V, and thereby its charge capacity (mAh/g), discharge capacity (mAh/g), and initial charge/discharge efficiency (%) were obtained.

[0131] Additionally, each of the coin cells, which were prepared per sample in Preparation Example above, were charged and discharged once. Then, from the second cycle of charge and discharge, each coin cell was charged with a static current 0.5 C until the voltage reached 0.005 V and then discharged with a static current 0.1 C until the voltage reached 2.0 V, and thereby its cycle characteristics (capacity maintaining rate) were obtained.

[0132] The charge and discharge capacities, the initial charge/discharge efficiency, and the capacity maintaining rate are shown in Table 2 below.

TABLE-US-00002 TABLE 2 Example Comparative Example 1 2 3 4 1 2 3 Initial Charge 1,382 1,460 1,556 1,257 1,224 1,143 1,647 Capacity (mAh/g) Initial Efficiency (%) 82.1 79.8 78.1 85.2 85.9 87.4 74.7 Capacity 84.6 89.3 88.4 80.2 76.1 74.7 90.1 Maintaining Rate (0.2 C, @50 cycles, %)

[0133] As shown in Table 2 above, the initial discharge capacity in Example 1 was 1,382 mAh/g which is lower than 1,647 mAh/g of Comparative Example 3, whereas the initial charge/discharge efficiency in Example 1 was higher than in Comparative Example 3, and the initial discharge capacity was lowest in Comparative Example 2.

[0134] Mg.sub.xSiO.sub.y produced by a reaction of magnesium with silicon oxide is known to be electrochemically inert, and it is speculated that as the Mg content increases in Comparative Example 1 than in Example 1, the electrochemically inert Mg.sub.xSiO.sub.y is produced in a larger quantity, thereby reducing the charge/discharge capacity.

[0135] Although the voltage in the charging process in FIG. 12 was 0.1 V or less, it was confirmed that the overvoltage was formed to be high as the magnesium content increased.

[0136] The dQ/dV, when the charge/discharge process was performed two cycles and 100 cycles, was measured using the batteries prepared in Examples and Comparative Examples of the present disclosure, and the results are shown in FIG. 12.

[0137] As shown in FIG. 11, in the case of Examples of the present disclosure, it was confirmed that the peak at around 0.45 V was greater than the peak at 0.25 V in the dQ/dV curve when the battery was charged twice.

<Experimental Example> Measurement of Volume Change According to Charge/Discharge

[0138] After performing 100 cycles of charge/discharge experiments on the battery prepared in Preparation Example, SEM analysis of the electrode and XRD analysis of the particles was performed, and the results are shown in Table 3 below.

TABLE-US-00003 TABLE 3 Example 1 Comparative Example 1 Pristine (μm) 23  18 After Cycle (μm) 33  40 Difference (μm) 10  22 Swelling Ratio (%) 44 122

[0139] As shown in Table 3 above, while the thickness of the electrode before charge/discharge was 23 μm and it changed to 33 μm after 100 cycles of charge/discharge in Example 1, the thickness of the electrode was 18 μm before charge/discharge and it changed to 40 μm after 100 cycles of charge/discharge in Comparative Example 1. Therefore, it was confirmed that in the case of the silicon composite oxide of Example 1, the volume change was reduced compared to Comparative Example 1.

<Experimental Example> Ex Situ XRD Measurement Before and After Charge/Discharge

[0140] Ex-situ XRD was measured for the batteries including the silicon composite particles of Example 1 and Comparative Example 1 after one cycle of charge/discharge and 100 cycles of charge/discharge, and the results are shown in FIG. 13.

[0141] As shown in FIG. 13, in the case of Example 1, no peak was observed except the peak shown by MgSiO.sub.3 and copper used as the current collector after one cycle of charge/discharge, and lithium hydroxide or lithium oxide peaks were observed after 100 cycles of charge/discharge. In contrast, as shown in FIG. 13, in the case of Comparative Example 1, although no peak was observed except the peak shown by Mg.sub.2SiO.sub.4 after one cycle of charge/discharge as in Example 1, peaks similar to the initial particle appeared after 100 cycles of charge/discharge.

[0142] In FIG. 13, in the case of Examples of the present disclosure, it was confirmed that the XRD peak derived from Mg.sub.xSiO.sub.y did not appear after two rounds of discharge.

[0143] The XRD results of Example 1, Comparative Example 1, and Comparative Example 3 after 100 cycles of charge/discharge are shown in FIG. 14. In FIG. 14, it was confirmed that LiOH was detected only in Comparative Example 3 and Example 1.

<Experimental Example> TEM, STEM-HAADF, and STEM-EDX Measurement

[0144] TEM, STEM-HAADF, and STEM-EDS were measured for the particles of Example 1, Example 2, and Comparative Example 3, and the results are shown in FIG. 15.

[0145] In FIG. 15, in the case of Comparative Example 3 in which Mg was not mixed, annular patterns corresponding to Si (111) and Si (220) were formed.

[0146] In the case of Example 1, unlike Comparative Example 3, the crystal structure was formed to be wider than Comparative Example 3, and MgSiO.sub.3 spots appeared. In contrast, in the case of Comparative Example 1, the non-crystalline portion appeared to be narrower than Comparative Example 3 and Example 1, and most of it was observed to be crystalline, and it was confirmed that a grain boundary between Si and Mg.sub.2SiO.sub.4 clearly appeared, as shown in FIG. 15c.

[0147] As shown in FIGS. 15e and 15h, in the case of Example 1, SiO.sub.x was formed around Si as a core shell structure. In contrast, as shown in FIGS. 15f and 15i, in the case of Comparative Example 1, it could be seen that the crystal structures of Example 1 and Comparative Example 1 were completely different because the Si and Mg.sub.xSiO.sub.y portions were clearly separated.

[0148] Based on the analysis results above, FIG. 10 shows schematic diagrams of the cross-section of the components of the prepared particles.

[0149] The carbon component is shown in black, the silicon oxide is shown in orange, the silicon component is shown in green, and the magnesium silicate is shown in blue.

<Experimental Example> EDS Photo Measurement Before and After Charge/Discharge

[0150] EDX was measured for the cells including the particles of Example 1, Example 2, and Comparative Example 3 after one charge/discharge and after 100 cycles of charge/discharge, and the results are shown in FIG. 16.

[0151] In the case of Example 1 in which the Mg content was 8%, the particles aggregated in the form of Mg.sub.xSiO.sub.y around the Si core after one cycle of charge/discharge as shown in FIGS. 16(a) to 16(d), Mg.sub.xSiO.sub.y was evenly distributed within the particles and became stable after 100 cycles of charge/discharge. In contrast, as shown in FIGS. 16(e) to 16(h), in the case of Comparative Example 1, it could be seen that the Mg.sub.xSiO.sub.y and Si domains were formed to be large from the beginning, and the lifetime characteristics were deteriorated due to the change in volume according to charge/discharge due to the structural change to obtain a stable form.

[0152] Such structural changes are schematically shown in FIG. 17.

[0153] As such, specific parts of the present disclosure have been described in detail, it will be apparent to those of ordinary skill in the art that these specific descriptions are merely preferred embodiments, and the scope of the present disclosure is not limited by these embodiments. Accordingly, the actual scope of the present disclosure will be defined by the appended claims and the equivalents thereof.