Method of Producing Elastomer Composite-Encapsulated Particles of Anode Active Materials for Lithium Batteries

a lithium battery and active material technology, applied in the field of rechargeable lithium batteries, can solve the problems of severe pulverization (fragmentation of alloy particles), loss of contacts between active material particles and conductive additives, etc., and achieves the effect of faster lithium ion transport and easy encapsulation

Pending Publication Date: 2019-08-29
GLOBAL GRAPHENE GRP INC
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

The patent describes a new type of material that can be used in batteries. It has many tiny layers of carbon arranged on top of each other. These small layers help make it work better than traditional materials like plastics. This makes them ideal for use in battery technology.

Problems solved by technology

This patent describes various methods for preparing an anode active material for lithium-ion batteries. Current methods involve adding certain chemical substances to the electrode, which leads to impurities called residual materials. Specifically, the patent discusses the issue of fast capacity fade over time and the lack of suitable reversable capacitor behavior.

Method used

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  • Method of Producing Elastomer Composite-Encapsulated Particles of Anode Active Materials for Lithium Batteries
  • Method of Producing Elastomer Composite-Encapsulated Particles of Anode Active Materials for Lithium Batteries
  • Method of Producing Elastomer Composite-Encapsulated Particles of Anode Active Materials for Lithium Batteries

Examples

Experimental program
Comparison scheme
Effect test

example 1

Graphene Oxide From Sulfuric Acid Intercalation and Exfoliation of MCMBs

[0119]MCMB (mesocarbon microbeads) were supplied by China Steel Chemical Co. This material has a density of about 2.24 g / cm3 with a median particle size of about 16 μm. MCMBs (10 grams) were intercalated with an acid solution (sulfuric acid, nitric acid, and potassium permanganate at a ratio of 4:1:0.05) for 48 hours. Upon completion of the reaction, the mixture was poured into deionized water and filtered. The intercalated MCMBs were repeatedly washed in a 5% solution of HCl to remove most of the sulfate ions. The sample was then washed repeatedly with deionized water until the pH of the filtrate was neutral. The slurry was dried and stored in a vacuum oven at 60° C. for 24 hours. The dried powder sample was placed in a quartz tube and inserted into a horizontal tube furnace pre-set at a desired temperature, 800° C.-1,100° C. for 30-90 seconds to obtain graphene samples. A small quantity of graphene was mixed wi

example 2

Oxidation and Exfoliation of Natural Graphite

[0120]Graphite oxide was prepared by oxidation of graphite flakes with sulfuric acid, sodium nitrate, and potassium permanganate at a ratio of 4:1:0.05 at 30° C. for 48 hours, according to the method of Hummers [U.S. Pat. No. 2,798,878, Jul. 9, 1957]. Upon completion of the reaction, the mixture was poured into deionized water and filtered. The sample was then washed with 5% HCl solution to remove most of the sulfate ions and residual salt and then repeatedly rinsed with deionized water until the pH of the filtrate was approximately 4. The intent was to remove all sulfuric and nitric acid residue out of graphite interstices. The slurry was dried and stored in a vacuum oven at 60° C. for 24 hours.

[0121]The dried, intercalated (oxidized) compound was exfoliated by placing the sample in a quartz tube that was inserted into a horizontal tube furnace pre-set at 1,050° C. to obtain highly exfoliated graphite. The exfoliated graphite was dispersed

example 3

Preparation of Pristine Graphene Sheets

[0122]Pristine graphene sheets were produced by using the direct ultrasonication or liquid-phase exfoliation process. In a typical procedure, five grams of graphite flakes, ground to approximately 20 μm in sizes, were dispersed in 1,000 mL of deionized water (containing 0.1% by weight of a dispersing agent, Zonyl® FSO from DuPont) to obtain a suspension. An ultrasonic energy level of 85 W (Branson S450 Ultrasonicator) was used for exfoliation, separation, and size reduction of graphene sheets for a period of 15 minutes to 2 hours. The resulting graphene sheets were pristine graphene that had never been oxidized and were oxygen-free and relatively defect-free. There are substantially no other non-carbon elements.

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Abstract

A method of producing a powder mass for a lithium battery, the method comprising: (a) mixing graphene sheets and an elastomer or its precursor in a liquid medium or solvent to form a suspension; (b) dispersing a plurality of particles of an anode active material in the suspension to form a slurry; and (c) dispensing the slurry and removing the solvent and/or polymerizing/curing the precursor to form the powder mass, wherein the powder mass comprises multiple particulates of the anode active material, wherein at least one of the particulates is composed of one or a plurality of the particles encapsulated by a thin layer of graphene/elastomer composite having a thickness from 1 nm to 10 μm, a lithium ion conductivity from 10−7 S/cm to 10−2 S/cm and an electrical conductivity from 10−7 S/cm to 100 S/cm.

Description

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Claims

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Application Information

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Owner GLOBAL GRAPHENE GRP INC
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