LITHIUM-CARBON COMPOSITE MATERIAL AND PREPARATION THEREOF

Abstract

A lithium-carbon composite material and a preparation method thereof. The method includes preparation of a micron lithium powder dispersion, adjustment of the solid content of the micron lithium powder dispersion, preparation of a lithium-carbon mixture, and preparation of the lithium-carbon composite material.

Claims

1. A method of preparing a lithium-carbon composite material, comprising: (S1) dispersing metal lithium in an organic solvent through liquid phase buoyancy to obtain a micron lithium powder dispersion; (S2) allowing the micron lithium powder dispersion obtained in step (S1) to stand, and removing a part of the organic solvent from the micron lithium powder dispersion such that a lithium powder solid content of the micron lithium powder dispersion is 25%-35%; (S3) adding carbon powder to the micron lithium powder dispersion obtained through step (S2) followed by cyclical grinding using a sand mill to disperse the carbon powder and lithium powder evenly to obtain a mixed system, wherein a molar ratio of Li to C is (3-4):1; and (S4) allowing the organic solvent in the mixed system to evaporate such that the carbon powder in the mixed system is carried by evaporated organic solvent and then settles to cover a surface of the lithium powder to obtain the lithium-carbon composite material.

2. The method of claim 1, wherein the steps (S1)-(S4) are all performed in an argon atmosphere.

3. The method of claim 2, wherein the step (S1) is performed through steps of: cutting the metal lithium into pieces followed by continuous feeding to a liquid-phase dispersion machine with the organic solvent and stirring, wherein a weight ratio of the metal lithium to the organic solvent is 3.55:96.45; heating, by a heating device of the liquid-phase dispersion machine, a mixture of the metal lithium and the organic solvent to 180° C.-190° C. under stirring such that the metal lithium melts to form uniformly dispersed micron lithium droplets in the organic solvent; allowing a mixture of the micron lithium droplets and the organic solvent to pass through a built-in 400-800 mesh sieve of the liquid-phase dispersion machine to enter a cooling device of the liquid-phase dispersion machine; and cooling the mixture of the micron lithium droplets and the organic solvent to room temperature such that the micron lithium droplets solidify to form lithium powder with a particle size of 20-40 μm in the organic solvent to obtain the micron lithium powder dispersion.

4. The method of claim 3, wherein in step (S1), the organic solvent is selected from the group consisting of undecane, dodecane, tridecane, tetradecane, pentadecane and a combination thereof.

5. The method of claim 2, wherein the carbon powder is selected from the group consisting of superconducting carbon black, conductive graphite, carbon fiber, carbon nanotube, graphene and a combination thereof.

6. The method of claim 2, wherein the step (S4) is performed through a step of: drying the mixed system obtained in step (S3) at 100° C.-150° C. and a pressure of −0.08 MPa to −0.1 MPa in a rake vacuum dryer to evaporate the organic solvent to obtain the lithium-carbon composite material.

7. A lithium-carbon composite material prepared according to the method of claim 1, wherein the lithium-carbon composite material is applied to a negative plate of a lithium-manganese dioxide primary battery.

8. The lithium-carbon composite material of claim 7, wherein the steps (S1)-(S4) are all performed in an argon atmosphere.

9. The lithium-carbon composite material of claim 8, wherein the step (S1) is performed through steps of: cutting the metal lithium into pieces followed by continuous feeding to a liquid-phase dispersion machine with the organic solvent and stirring, wherein a weight ratio of the metal lithium to the organic solvent is 3.55:96.45; heating, by a heating device of the liquid-phase dispersion machine, a mixture of the metal lithium and the organic solvent to 180° C.-190° C. under stirring such that the metal lithium melts to form uniformly dispersed micron lithium droplets in the organic solvent; allowing a mixture of the micron lithium droplets and the organic solvent to pass through a built-in 400-800 mesh sieve of the liquid-phase dispersion machine to enter a cooling device of the liquid-phase dispersion machine; and cooling the mixture of the micron lithium droplets and the organic solvent to room temperature such that the micron lithium droplets solidify to form lithium powder with a particle size of 20-40 μm in the organic solvent to obtain the micron lithium powder dispersion.

10. The lithium-carbon composite material of claim 10, wherein in step (S1), the organic solvent is selected from the group consisting of undecane, dodecane, tridecane, tetradecane, pentadecane and a combination thereof.

11. The lithium-carbon composite material of claim 8, wherein the carbon powder is selected from the group consisting of superconducting carbon black, conductive graphite, carbon fiber, carbon nanotube, graphene and a combination thereof.

12. The lithium-carbon composite material of claim 8, wherein the step (S4) is performed through a step of: drying the mixed system obtained in step (S3) at 100° C.-150° C. and a pressure of −0.08 MPa to −0.1 MPa in a rake vacuum dryer to evaporate the organic solvent to obtain the lithium-carbon composite material.

Description

BRIEF DESCRIPTION OF THE DRAWINGS

[0026] This FIGURE schematically illustrates comparison of a lithium manganese primary battery whose anode active material is made of a lithium-carbon composite material of the disclosure and a traditional lithium manganese battery in the discharge performance.

DETAILED DESCRIPTION OF EMBODIMENTS

[0027] In order to promote the understanding of the present disclosure, the disclosure will be described below in detail with reference to the embodiments and accompanying drawings. It should be understood that the embodiments are merely illustrative, and are not intended to limit the scope of the present disclosure.

[0028] The present disclosure provides a method for preparing a lithium-carbon composite material, which is described as follows.

[0029] (S1) Preparation of micron lithium powder dispersion

[0030] The metal lithium is dispersed in an organic solvent through the liquid phase buoyancy to obtain a micron lithium powder dispersion.

[0031] (S2) Adjustment of solid content of the lithium dispersion

[0032] The micron lithium powder dispersion obtained in step (S1) is allowed to stand, and a part of the organic solvent is removed so that the lithium powder solid content of the dispersion is −25%-35%.

[0033] (S3) Preparation of lithium-carbon mixed system

[0034] The micron lithium powder dispersion obtained in step (S2) is added with carbon powder and subjected to cyclical grinding with a sand mill to fully disperse the carbon powder and lithium powder to obtain a mixed system, where a molar ratio of Li to C is (3-4):1.

[0035] (S4) Preparation of lithium-carbon composite material

[0036] The organic solvent in the mixed system is evaporated such that the carbon powder in the mixed system is carried by evaporated organic solvent and then settles to cover a surface of the lithium powder to obtain the lithium-carbon composite material.

[0037] In an embodiment, the above steps (S1)-(S4) are all performed in an argon atmosphere.

[0038] In an embodiment, the step (S1) is performed through the following steps.

[0039] The metal lithium is cut into pieces followed by continuous feeding to a liquid-phase dispersion machine with the organic solvent and stirred, where a weight ratio of the metal lithium to the organic solvent is 3.55:96.45. A mixture of the metal lithium and the organic solvent under stirring is heated to 180° C.-190° C. by a heating device of the liquid-phase dispersion machine, such that the metal lithium melts to form uniformly dispersed micron lithium droplets in the organic solvent. A mixture of the micron lithium droplets and the organic solvent is allowed to pass through a built-in 400-800 mesh sieve of the liquid-phase dispersion machine to enter a cooling device of the liquid-phase dispersion machine. The mixture of the micron lithium droplets and the organic solvent is cooled to room temperature such that the micron lithium droplets solidify to form lithium powder with a particle size of 20-40 μm in the organic solvent to obtain the micron lithium powder dispersion.

[0040] In an embodiment, in step (S1), the organic solvent is selected from the group consisting of undecane, dodecane, tridecane, tetradecane, pentadecane and a combination.

[0041] In an embodiment, the carbon powder is selected from the group consisting of superconducting carbon black, conductive graphite, carbon fiber, carbon nanotube, graphene and a combination.

[0042] In an embodiment, the step (S4) is performed through the following step.

[0043] The mixed system obtained in step (S3) at 100° C.-150° C. and a pressure of −0.08 MPa to −0.1 MPa is dried in a rake vacuum dryer to evaporate the organic solvent to obtain the lithium-carbon composite material.

[0044] As shown in the FIGURE, the curve A shows the discharge characteristic of a lithium manganese primary battery whose negative plate includes the lithium-carbon composite material prepared by the above method, and the curve B shows the discharge characteristic of a traditional lithium manganese battery which employs a metallic lithium strip as the negative plate. It can be seen from the FIGURE that under the same operation temperature, the discharge voltage plateau and discharge capacity of the lithium manganese battery primary containing the lithium-carbon composite material of the present disclosure at 0.2 C are respectively higher than the discharge voltage plateau and discharge capacity of the traditional lithium manganese primary battery at 0.1 C.

[0045] Described above are merely preferred embodiments of the disclosure, which are not intended to limit the disclosure. It should be noted that any changes, modifications and replacements made by those skilled in the art without departing from the spirit of the disclosure should fall within the scope of the disclosure defined by the appended claims.