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Lithium ion battery composite negative electrode material ZrO2 and preparation method thereof

A lithium-ion battery and negative electrode material technology, applied in battery electrodes, secondary batteries, nanotechnology for materials and surface science, etc., can solve the problems of good monodispersity, fast capacity decay, and low specific capacity, and achieve The preparation process is simple and feasible, good cycle stability, and the effect of inhibiting particle agglomeration

Inactive Publication Date: 2019-01-01
YANGTZE UNIVERSITY
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0004] The purpose of the present invention is to overcome the problems of low specific capacity, fast capacity fading, and poor cycle stability of the assembled battery in the prior art, and provides a lithium ion battery composite negative electrode material ZrO 2 and preparation method thereof, the lithium-ion battery composite negative electrode material ZrO 2 Good monodispersity, the first charge and discharge efficiency reaches 63.8%, after 100 cycles, its capacity retention rate is 85%, and the assembled battery has good cycle stability

Method used

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  • Lithium ion battery composite negative electrode material ZrO2 and preparation method thereof
  • Lithium ion battery composite negative electrode material ZrO2 and preparation method thereof
  • Lithium ion battery composite negative electrode material ZrO2 and preparation method thereof

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Embodiment 1

[0028] First, use zirconium n-butoxide as zirconium source, disperse it in a certain volume of n-butanol, keep stirring the n-butanol solution containing zirconium alcohol at 40°C, and obtain a uniform solution after 30 minutes; then remove a certain volume of n-butanol solution Add ionized water into a certain volume of n-butanol, ultrasonically disperse it for 30 minutes, then add it into the above-mentioned zirconium alcohol alcohol solution at a speed of 10d / s, and control v (zirconium source): v (deionized water): v (n-butanol Alcohol) = 2: x: 80 (x = 0.5, 1, 1.5, 2); after reacting at 40°C for 1 hour, the temperature was raised to 60°C to start aging, and the whole aging process lasted for 8 hours. After the reaction is completed, after centrifugal washing and vacuum drying, ZrO can be obtained. 2 Precursor. Then place the precursor in an argon atmosphere for calcination, keep the temperature at 900°C for 5 hours, and cool down with the furnace to obtain the target prod...

Embodiment 2

[0033] First, use zirconium n-butoxide as zirconium source, disperse it in a certain volume of n-butanol, keep stirring the n-butanol solution containing zirconium alcohol at 40°C, and obtain a uniform solution after 30 minutes; then remove a certain volume of n-butanol solution Add ionized water into a certain volume of n-butanol, ultrasonically disperse it for 30 minutes, then add it into the above-mentioned zirconium alcohol alcohol solution at a speed of 10d / s, and control v (zirconium source): v (NaCl solution): v (n-propanol )=2:1:80; after reacting at 40°C for 1 hour, the temperature was raised to 60°C to start aging, and the whole aging process lasted for 8 hours. After the reaction is completed, after centrifugal washing and vacuum drying, ZrO can be obtained. 2 Precursor. Then place the precursor in an inert atmosphere for calcination, and calcine at a constant temperature of 600, 700, 900, 1000 and 1100°C for 5 hours, and cool down with the furnace to obtain the ta...

Embodiment 3

[0038] First, zirconium n-butoxide is used as the source of zirconium, which is dispersed in a certain volume of n-butanol, and the n-butanol solution containing zirconium alcohol is continuously stirred at 40°C, and a uniform solution is obtained after 30 minutes; then a certain volume of aqueous solution ( Deionized water, NaCl solution, NaOH solution and CH 3 COOH solution) was added to a certain volume of n-butanol, ultrasonically dispersed for 30 minutes and then added to the above-mentioned zirconium alcohol alcohol solution at a speed of 10d / s, and v (zirconium source): v (NaCl solution): v (n-propyl Alcohol) = 2:1:80; after reacting at 40°C for 1 hour, the temperature was raised to 60°C to start aging, and the whole aging process lasted for 8 hours. After the reaction is completed, after centrifugal washing and vacuum drying, ZrO can be obtained. 2 Precursor. Then place the precursor in an inert atmosphere for calcination, calcine at a constant temperature of 900 ° C...

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Abstract

The invention provides a lithium ion battery composite negative electrode material ZrO2 and a preparation method thereof. The method concretely comprises the following steps of under the condition ofinert atmosphere, a water alcoholic solution is dripped into an alcoholic solution containing zirconium alcohol; after the continuous stirring for a period of time, performing centrifugation on the obtained solution to obtain ZrO2 precipitates; then, performing repeated washing and centrifugation on the precipitates; putting the precipitates into a vacuum drying box to be dried for a period of time to obtain nanometer ZrO2 precursors; performing controlled temperature roasting on the nanometer ZrO2 precursors at a certain temperature for a certain time; performing cooling along with the furnace to obtain the lithium ion battery composite negative electrode material ZrO2. The prepared negative electrode material has the advantages that the particle dimension is between 90 and 250 nm; the first time charging and discharging efficiency reaches 63.8 percent; after 100 times of circulation, the volume maintaining rate is 85 percent; the preparation process is simple; the implementation is easy.

Description

technical field [0001] The invention relates to the field of lithium-ion battery materials and preparation methods thereof, in particular to a lithium-ion battery composite negative electrode material ZrO 2 and its preparation method. Background technique [0002] ZrO 2 , chemical properties are inactive, and have high melting point, low thermal expansion coefficient, high refractive index, high resistivity, and good biocompatibility, making it an important high temperature resistant material and other functions. For example ZrO 2 The fiber is a polycrystalline refractory fiber material, which has a higher service temperature than other refractory fibers such as alumina fiber and aluminum silicate fiber. At present, it is the top refractory fiber material in the world. [0003] Environmental pollution, resource shortage, and energy crisis are the three severe challenges facing human existence. Finding non-polluting, renewable, and resource-saving secondary resources is a...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): C01G25/02H01M4/48H01M10/0525B82Y30/00
CPCB82Y30/00C01G25/02C01P2004/03C01P2006/40H01M4/483H01M10/0525Y02E60/10
Inventor 肖围李锐缪畅王脂胭
Owner YANGTZE UNIVERSITY