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Negative electrode carbon material for nonaqueous secondary battery, negative electrode, and nonaqueous secondary battery

A secondary battery and negative electrode material technology, applied in secondary batteries, non-aqueous electrolyte batteries, battery electrodes, etc., can solve the problems of small reversible capacity, increase of irreversible capacity for charging and discharging, and failure to achieve high capacity, etc., to achieve charging and discharging Excellent rate characteristics, less expansion and gas generation, and less deterioration

Active Publication Date: 2017-09-08
MITSUBISHI RAYON CO LTD
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, amorphous carbon materials have a small reversible capacity within the range of materials that can be used in practical use. In addition, when graphite materials increase the density of the active material layer containing the negative electrode material in order to increase the capacity, the initial stage will be damaged due to material destruction. The charge-discharge irreversible capacity during cycling increases, and as a result, there is a problem that high capacity cannot be achieved

Method used

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  • Negative electrode carbon material for nonaqueous secondary battery, negative electrode, and nonaqueous secondary battery
  • Negative electrode carbon material for nonaqueous secondary battery, negative electrode, and nonaqueous secondary battery

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preparation example Construction

[0132] The firing temperature varies depending on the organic compound used in the preparation of the mixture, but in the case of obtaining a composite carbon material (A) coated with (amorphous) carbonaceous substance or graphite substance, it is usually heated to 500°C Above, preferably at 800°C or above, more preferably at 900°C or above, the organic compound is sufficiently carbonized. The upper limit of the heating temperature is the temperature at which the carbide of the organic compound does not attain a crystal structure equivalent to that of the raw carbon material (a) in the mixture, and is usually at most 3000°C or less, preferably 2000°C or less, more preferably 1500°C or less. below ℃.

[0133] In the firing treatment conditions, thermal history temperature conditions, heating rate, cooling rate, heat treatment time, and the like are appropriately set. Alternatively, heat treatment may be performed in a relatively low temperature region, and then the temperature...

Embodiment 1

[0248] Using spheroidized natural graphite as the raw carbon material, use a CIP molding machine at 1000kgf / cm 2 After performing isotropic pressure treatment for 2 minutes, it was crushed and mixed with petroleum-based heavy oil (easily graphitizable organic compound) obtained during thermal cracking of naphtha with a twin-screw kneader. Then the resulting mixture is heat-treated at 700°C for 2 hours in an inert gas, and then heat-treated at 1300°C for 1 hour to obtain carbonaceous substances with different crystallinity coated on the surface of the spheroidized natural carbon material Composite carbon material (A) as a multilayer carbon structure. Here, the composite carbon material (A) has a volume-based average particle diameter (d50) of 23.0 μm and a BET specific surface area (SA) of 1.9 m 2 / g, tap density (tap) is 1.17g / cm 3 , Raman R value is 0.36.

[0249] It should be noted that the porosity in the particles after the isotropic pressurization treatment was 18%, an...

Embodiment 2

[0266] Use spheroidized natural graphite as the raw carbon material, and use a CIP molding machine at 1000kgf / cm 2After carrying out isotropic pressure treatment for 2 minutes, crushing was carried out, and this was mixed with petroleum-based heavy oil (easily graphitizable organic compound) obtained during thermal cracking of naphtha by a twin-screw kneader. Next, the resulting mixture was heat-treated at 700°C for 2 hours in an inert gas, and then heat-treated at 1300°C for 1 hour to obtain a carbonaceous material with different crystallinity coated on the surface of the spheroidized natural carbon material. The multilayer carbon structure of the material is the composite carbon material (A). Here, the composite carbon material (A) has a volume-based average particle diameter (d50) of 16.8 μm and a BET specific surface area (SA) of 3.1 m 2 / g, tap density (tap) is 1.17g / cm 3 , Raman R value is 0.27.

[0267] As the carbon material (B), a d50 of 10.9 μm and an SA of 8.8 m ...

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Abstract

An object of the present invention is to provide a negative electrode material for a non-aqueous secondary battery having excellent output and cycle characteristics by producing a high-density negative electrode active material without damaging the surface structure. The negative electrode material for a non-aqueous secondary battery according to the present invention includes a composite carbon material obtained by coating a pressurized carbon material with a carbonaceous substance or a graphite substance, and a carbon material specified below. Carbon material: one or more carbon materials selected from natural graphite, artificial graphite, coated graphite obtained by coating raw carbon material not subjected to pressure treatment with a carbonaceous substance or graphite substance, and amorphous carbon.

Description

technical field [0001] The present invention relates to a negative electrode carbon material for a nonaqueous secondary battery used in a nonaqueous secondary battery, a negative electrode formed using the carbon material, and a nonaqueous secondary battery including the negative electrode. Background technique [0002] In recent years, along with miniaturization of electronic equipment, the demand for high-capacity secondary batteries has been increasing. In particular, lithium-ion secondary batteries, which have higher energy density and better high-current charge-discharge characteristics than nickel-cadmium batteries and nickel-metal hydride batteries, are attracting attention. [0003] As negative electrode materials for lithium ion secondary batteries, graphite materials or amorphous carbon are often used in view of cost and durability. However, amorphous carbon materials have a small reversible capacity within the range of materials that can be used in practical use....

Claims

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Application Information

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Patent Type & Authority Patents(China)
IPC IPC(8): H01M4/583H01M4/133H01M4/36
CPCH01M4/133H01M4/1393H01M4/366H01M4/587H01M10/0525H01M2004/021Y02E60/10H01M4/36H01M4/583H01M10/05
Inventor 长山大悟斋藤阳介横沟正和布施亨
Owner MITSUBISHI RAYON CO LTD