IP Library Granted Patent US 10,862,115
Granted Patent B2
US 10,862,115 · App. 15/573,669 · Granted Dec 8, 2020

Anode material for secondary battery and non-aqueous electrolyte secondary battery using the same

Inventors: Keiko Matsubara (Tokyo, JP); Yoshiyuki Igarashi (Tokyo, JP)
H01M4/386H01M4/0488H01M4/134H01M4/38H01M4/583H01M4/62H01M4/625H01M10/0525H01M2004/027
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Quick Facts
Patent No.
US 10,862,115
App. No.
15/573,669
Granted
Dec 8, 2020
Kind
B2
Abstract

Provided is an anode material for a secondary battery which reduces and inhibits swelling of a high-capacity silicon-containing alloy material to realize excellent charge/discharge cycle characteristics. The anode material includes alloy particles containing a transition metal which has electron conductivity, is difficult to react with lithium atoms and is at least one selected from the group of metals that belong to transition metals, and silicon, wherein the alloy particles include amorphous silicon, and silicide microcrystals formed by silicon and the transition metal, and the silicide microcrystals are scattered in amorphous silicon.

Claims (25)

1. A secondary battery, comprising:

a cathode;

an anode comprising an anode material;

a non-aqueous electrolyte; and

a separator,

wherein the anode material, prior to an initial charge/discharge cycle of the secondary battery, comprises:

a composite comprising alloy particles and a carbonaceous material, wherein the composite is prepared by mechanical alloying of the alloy particles and the carbonaceous material,

wherein the alloy particles containing amorphous silicon, and silicide microcrystals containing silicon and a transition metal,

wherein the silicide microcrystals are scattered in the amorphous silicon,

wherein the transition metal has electron conductivity, and is difficult to react with lithium atoms, and

wherein the silicon present in the alloy particles is present in the silicide microcrystals and the amorphous silicon, and

wherein the diffraction peak of (111) surface of silicon is not identified in the alloy particles after formation of the composite when measured by X-ray diffractometry.

2. The secondary battery according to claim 1 , wherein the silicide microcrystals have a crystallite size of 5-100 nm.

3. The secondary battery according to claim 1 , wherein the silicide microcrystals have a crystal lattice of 5-20 Å.

4. The secondary battery according to claim 1 , wherein the transition metal is any one selected from the group consisting of Ti, V, Cr, Mn, Fe, Co, Ni, W, Nb and Cu, or a mixture thereof.

5. The secondary battery according to claim 1 , wherein the content of amorphous silicon contained in the alloy particles is 10-60 wt %.

6. The secondary battery according to claim 1 , wherein the anode material has a 50% particle diameter of 1-5 μm in a volume accumulated particle size distribution, and the anode material has a 90% particle diameter of 5-30 μm in a volume accumulated particle size distribution.

7. The secondary battery according to claim 1 , wherein the anode further comprising a conductive material, wherein the conductive material comprises carbon nanotubes.

8. The secondary battery according to claim 7 , wherein the conductive material is present in an amount of 0.1 weight percent (wt %) to 5 wt % based on the total weight of the anode for a secondary battery.

9. The secondary battery according to claim 1 , which is a lithium secondary battery.

10. A method for preparing the anode material for a secondary battery as defined in claim 1 , comprising:

heating a transition metal and silicon to a liquid state;

cooling the heated transition metal and silicon to form a parent alloy containing a silicide containing silicon and the transition metal and crystalline silicon;

mechanically alloying the parent alloy to form the alloy particles including the amorphous silicon, and silicide microcrystals, where the mechanical alloying inhibits crystallization of amorphous silicon such that the diffraction peak of (111) surface of silicon is not identified in the alloy particles when measured by X-ray diffractometry; and

mechanically alloying the alloy particles and a carbonaceous material to form a composite, wherein the mechanical alloying to form the composite is different from the mechanical alloying used to form the alloy particles, and wherein the diffraction peak of (111) surface silicon is not identified in the alloy particles after formation of the composite.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 4, 2021
From: LG CHEM, LTD.
To: LG ENERGY SOLUTION, LTD.
Reel/Frame 058295/0068 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 14, 2017
From: MATSUBARA, KEIKO; IGARASHI, YOSHIYUKI
To: LG CHEM, LTD.
Reel/Frame 044122/0262 →
Priority Claims (1)
JP 2015-110531 · May 29, 2015 · national
Continuity (1)
Related Publication 20180069237A1 · Mar 8, 2018