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Negative electrode material and preparation method thereof, negative electrode of lithium ion battery and lithium ion battery

A technology for lithium ion batteries and negative electrode materials, applied in battery electrodes, negative electrodes, secondary batteries, etc., can solve the problems of short life and poor rate performance of negative electrode materials, and achieve high rate performance, high electron affinity, and long life. Effect

Inactive Publication Date: 2019-01-04
GUANGDONG UNIV OF TECH
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] The invention provides a negative electrode material and a preparation method thereof, a lithium ion battery negative electrode and a lithium ion battery, and solves the technical problems of poor rate performance and short service life of the existing lithium ion battery negative electrode materials

Method used

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  • Negative electrode material and preparation method thereof, negative electrode of lithium ion battery and lithium ion battery
  • Negative electrode material and preparation method thereof, negative electrode of lithium ion battery and lithium ion battery
  • Negative electrode material and preparation method thereof, negative electrode of lithium ion battery and lithium ion battery

Examples

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Effect test

Embodiment 1

[0050]Accurately weigh 1.8g of manganese acetylacetonate and 0.8g of nitrilotriacetic acid and add them to a mixed solution of 5ml of deionized water and 35ml of isopropanol, stir and dissolve, then transfer to a reaction kettle, heat to 180°C and keep for 12 hours , centrifuged to collect the precipitate, and washed twice with ethanol and dried to obtain the manganese precursor nanowire; get 100mg manganese precursor nanowire and 50mg dopamine hydrochloride and join in 50ml tris(hydroxymethyl)aminomethane buffer solution, stir for 72 Hours, centrifuge to collect the precipitate, wash it twice with ethanol and dry it to obtain the dopamine-wrapped manganese nanowire intermediate; mix the dopamine-wrapped manganese nanowire intermediate with 3-methylthioaniline in a mass ratio of 1:4 Finally, after sintering at 450° C. for 2 hours in an argon atmosphere, a nitrogen-sulfur co-doped carbon-modified manganese sulfide composite negative electrode material is obtained.

Embodiment 2

[0052] Accurately weigh 2g of manganese sulfate and 1.2g of chitosan, add them to a mixed solution of 10ml of deionized water and 30ml of isopropanol, stir and dissolve, transfer to a reaction kettle, heat to 200°C and keep for 12 hours, centrifuge to collect the precipitate 50mg of manganese precursor nanowires and 100mg of dopamine hydrochloride were added to 50ml of tris(hydroxymethyl)aminomethane buffer, stirred for 24 hours, and centrifuged to collect the precipitate , and washed twice with ethanol and dried to obtain the dopamine-wrapped manganese nanowire intermediate; after mixing the dopamine-wrapped manganese nanowire intermediate with ammonium thiosulfate at a mass ratio of 2:1, the After sintering in the atmosphere for 4 hours, a nitrogen-sulfur co-doped carbon-modified manganese sulfide composite negative electrode material was obtained.

Embodiment 3

[0054] Accurately weigh 0.8g of manganese hypophosphite, 1g of manganese phosphate and 0.75g of acetonitrile and add them to a mixed solution of 65ml of deionized water and 15ml of isopropanol, stir and dissolve, then transfer to a reaction kettle, heat to 160°C and keep for 10 hour, centrifuge to collect the precipitate, and after drying twice with ethanol, obtain the manganese precursor nanowire; get 100mg manganese precursor nanowire and 50mg dopamine hydrochloride and join in the 50ml tris(hydroxymethyl)aminomethane buffer solution, stir After 72 hours, the precipitate was collected by centrifugation, washed twice with ethanol and dried to obtain the dopamine-wrapped manganese nanowire intermediate; after mixing the dopamine-wrapped manganese nanowire intermediate with liter sulfur in a mass ratio of 1:5, the °C and sintered in an argon atmosphere for 4 hours, a nitrogen-sulfur co-doped carbon-modified manganese sulfide composite anode material was obtained.

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Abstract

The invention relates to the technical field of lithium ion batteries, in particular to a negative electrode material and a preparation method thereof, a negative electrode of a lithium ion battery and a lithium ion battery. The invention discloses a negative electrode material, comprising: MnS particles and a carbon nanorod matrix loaded with MnS particles; The porous carbon nanorod matrix is a nitrogen-sulfur doped carbon nanorod matrix; The specific surface area of the negative electrode material is 60 m2g-1 - 170 m2g-1. As that manganese sulfide particle in the negative electrode materialare small and wrapped by nitrogen-sulfur co-doped carbon nanorod, the negative electrode material of the invention has excellent conductivity and large specific surface area, has high rate performanceand long service life, and solves the technical problems of poor rate performance and short service life of the negative electrode material of the prior lithium ion battery.

Description

technical field [0001] The invention relates to the technical field of lithium ion batteries, in particular to a negative electrode material and a preparation method thereof, a lithium ion battery negative electrode and a lithium ion battery. Background technique [0002] Currently, lithium-ion batteries are widely used in portable devices, electric vehicles, and large-scale energy storage devices. In the commercial lithium-ion battery system, graphite is mainly used as the anode material of lithium-ion batteries, but the theoretical specific capacity of graphite-based anode materials is only 372mAh g -1 , and the rate performance is poor, so the development of new high-performance anode materials has become the focus. [0003] In recent years, transition metal sulfides (TMS) have attracted considerable attention as anode materials for Li-ion batteries due to their high capacity, good electrical conductivity, and thermal stability relative to their oxide counterparts. When...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/36H01M4/58H01M4/62H01M4/136H01M10/0525
CPCH01M4/136H01M4/366H01M4/5815H01M4/625H01M10/0525H01M2004/021H01M2004/027Y02E60/10
Inventor 苏豪耿洪波李成超张宇斐
Owner GUANGDONG UNIV OF TECH