IP Library Granted Patent US 9,640,795
Granted Patent B2
US 9,640,795 · App. 14/116,253 · Granted May 2, 2017

Positive-electrode active material particle for all-solid battery and method for production thereof

Inventor: Takayuki Uchiyama (Susono, JP)
Assignee: TOYOTA JIDOSHA KABUSHIKI KAISHA
H01M4/366H01M4/0416H01M4/0419H01M4/134H01M4/136H01M4/505H01M4/525H01M4/581H01M4/5815H01M4/625H01M10/052H01M2004/028H01M2220/10H01M2220/20H01M2220/30Y02E60/122
View Patent ↗
Loading inventors, assignments & file history…
Monitor This Case
Get email alerts when status or documents change.
Order Certified Copies
Most orders are placed with the USPTO same day — all within 24 business hours.
Order via The Patent Place →
Pre-filled with this patent's details
Quick Facts
Patent No.
US 9,640,795
App. No.
14/116,253
Granted
May 2, 2017
Kind
B2
Abstract

A positive-electrode active material particle for an all-solid battery which includes a sulfide-based solid electrolyte includes an active material core and a reaction-inhibiting layer which contains carbon and with which the active material core is coated.

Claims (27)

1. A positive-electrode active material particle for an all-solid battery which includes a sulfide-based solid electrolyte, comprising:

a core of an active material particle having a size of about 0.5 to 10 μm; and

a reaction-inhibiting layer which contains carbon in a form of simple substance,

wherein the reaction-inhibiting layer coats an entire surface of the core of the active material particle, the reaction-inhibiting layer having a thickness of 1 to 100 nm,

wherein

the simple substance of carbon is dispersed uniformly in the reaction-inhibiting layer, and

wherein the reaction-inhibiting layer has a Raman spectrum including discernible peaks at 1340 cm −1 and 1590 cm −1 , wherein the Raman spectroscopic analysis conditions include excitation wavelength: 514.5 nm, laser power, 20 mW, laser spot diameter: 1 μm, exposure time: 30 seconds, number of times of integration: 8, diffraction lattice: 600 gr/mm, confocal hole diameter: 30 μm, conducted at room temperature.

2. The positive electrode active material particle according to claim 1 ,

wherein the reaction-inhibiting layer is holohyaline.

3. The positive electrode active material particle according to claim 2 ,

wherein the reaction-inhibiting layer includes one of a lithium conducting oxide and a composite oxide.

4. A production method for positive-electrode active material particles for an all-solid battery which includes a sulfide-based solid electrolyte, each of the positive-electrode active material particles comprising a core of an active material particle having a size of about 0.5 to 10 μm and a reaction-inhibiting layer which contains carbon in a form of simple substance, wherein the reaction-inhibiting layer coats an entire surface of the core of the active material particle, the reaction-inhibiting layer having a thickness of 1 to 100 nm, wherein the simple substance of carbon is dispersed uniformly in the reaction-inhibiting layer, and wherein the reaction-inhibiting layer has a Raman spectrum including discernible peaks at 1340 cm −1 and 1590 cm −1 , wherein the Raman spectroscopic analysis conditions include excitation wavelength: 514.5 nm, laser power: 20 mW, laser soot diameter: 1 μm, exposure time: 30 seconds, number of times of integration: 8, diffraction lattice: 600 gr/mm, confocal hole diameter: 30 μm, conducted at room temperature, the production method comprising:

preparing precursors of the reaction-inhibiting layers that each contain a carbon source and that inhibit a reaction between the sulfide-based solid electrolyte and the active material particles;

coating the core of the active material particles with the precursors of the reaction-inhibiting layers; and

performing a heat treatment on the cores of the active material particles that have been coated with the precursors of the reaction-inhibiting layers, in an atmosphere with an oxygen concentration of 50 vol % or higher, to form the positive-electrode active material particles.

5. The production method according to claim 4 ,

wherein the precursors of the reaction-inhibiting layers are prepared by mixing an organic acid lithium salt and a solution that forms a glass network.

6. The production method according to claim 4 ,

wherein the precursors of the reaction-inhibiting layers are prepared by mixing boric acid, tetraethoxysilane and an alcohol to prepare a solution in which a B—Si glass network has been formed by a hydrolysis reaction, and mixing the solution in which a B—Si glass network has been formed with an organic acid lithium salt.

7. The production method according to claim 5 ,

wherein the organic acid lithium salt is one of lithium acetate and lithium lactate.

8. The positive electrode active material particle according to claim 1 ,

wherein the core of the active material particle includes a lithium transition metal oxide.

9. The production method according to claim 4 ,

wherein the active material core includes a lithium transition metal oxide.

10. The positive electrode active material particle according to claim 3 ,

wherein the reaction-inhibiting layer comprises a lithium conducting oxide, a ratio of carbon atoms to lithium atoms in a starting composition used to form the reaction-inhibiting layer being C:Li=1:1 to 4:1.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Nov 7, 2013
From: UCHIYAMA, TAKAYUKI
To: TOYOTA JIDOSHA KABUSHIKI KAISHA
Reel/Frame 031660/0075 →
Priority Claims (1)
JP 2011-110132 · May 17, 2011 · national
Continuity (1)
Related Publication 20140072875A1 · Mar 13, 2014