A carbon @fe 2 o 3 @Carbon microsphere composite material and its application

A composite material and carbon microsphere technology, applied in structural parts, electrical components, battery electrodes, etc., can solve the problems of poor cycle life of negative electrode materials, and achieve the effect of improving cycle life, good reproducibility and simple process

Active Publication Date: 2022-03-01
JIANGSU UNIV OF SCI & TECH +1
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

[0004] The technical problem to be solved by the present invention is to provide a carbon@Fe 2 o 3 @Carbon microsphere composite material and its application to solve the technical problem of poor cycle life of the existing ferric oxide as lithium-ion battery anode material

Method used

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  • A carbon @fe  <sub>2</sub> o  <sub>3</sub> @Carbon microsphere composite material and its application
  • A carbon @fe  <sub>2</sub> o  <sub>3</sub> @Carbon microsphere composite material and its application
  • A carbon @fe  <sub>2</sub> o  <sub>3</sub> @Carbon microsphere composite material and its application

Examples

Experimental program
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Effect test

Embodiment 1

[0031] (1) Add 1.7ml TEOS and 4ml ammonia water to the mixed solution consisting of 15ml ethanol and 6ml water and stir for 1 hour. Subsequently, 0.4 g of resorcinol and 0.56 ml of formaldehyde were added, and stirring was continued for 24 h. Subsequently, the reaction solution was hydrothermally reacted at 100° C. for 24 h, and the product was collected by centrifugation and washed 4 times with ethanol. Get SiO 2 @Phenolic Resin.

[0032] (2) SiO after step (1) drying 2 @Phenolic resin is placed in a tube furnace, fed with nitrogen protection gas at an intake rate of 0.5L / min, firstly heated to 400°C at a rate of 6°C / min and kept for half an hour, then at a rate of 1°C / min Raise the temperature to 700°C and keep it for 2 hours to obtain SiO 2 @Carbon microspheres, then SiO 2 The @carbon was soaked in 15wt% hydrofluoric acid solution for 12 hours, then centrifuged to collect the product, and washed with water until neutral to obtain hollow carbon spheres.

[0033] (3) Ul...

Embodiment 2

[0040] (1) Add 2.2ml TEOS and 4ml ammonia water to the mixed solution consisting of 19ml ethanol and 8ml water and stir for 1 hour. Subsequently, 0.4 g of resorcinol and 0.56 ml of formaldehyde were added, and stirring was continued for 24 h. Subsequently, the reaction solution was hydrothermally reacted at 100° C. for 24 h, and the product was collected by centrifugation and washed 4 times with ethanol. Get SiO 2 @Phenolic Resin.

[0041] (2) SiO after step (1) drying 2 @Phenolic resin is placed in a tube furnace, fed with nitrogen protection gas at an intake rate of 0.5L / min, firstly heated to 400°C at a rate of 6°C / min and kept for half an hour, then at a rate of 1°C / min Raise the temperature to 700°C and keep it for 2 hours to obtain SiO 2 @Carbon microspheres, then SiO 2 The @carbon was soaked in 15wt% hydrofluoric acid solution for 12 hours, then centrifuged to collect the product, and washed with water until neutral to obtain hollow carbon spheres.

[0042] (3) Ul...

Embodiment 3

[0046] (1) Add 1.3ml TEOS and 4ml ammonia water to the mixed solution consisting of 12ml ethanol and 4ml water and stir for 1 hour. Subsequently, 0.4 g of resorcinol and 0.56 ml of formaldehyde were added, and stirring was continued for 24 h. Subsequently, the reaction solution was hydrothermally reacted at 100° C. for 24 h, and the product was collected by centrifugation and washed 4 times with ethanol. Get SiO 2 @Phenolic Resin.

[0047] (2) SiO after step (1) drying 2 @Phenolic resin is placed in a tube furnace, fed with nitrogen protection gas at an intake rate of 0.5L / min, firstly heated to 400°C at a rate of 6°C / min and kept for half an hour, then at a rate of 1°C / min Raise the temperature to 700°C and keep it for 2 hours to obtain SiO 2 @Carbon microspheres, then SiO 2 The @carbon was soaked in 15wt% hydrofluoric acid solution for 12 hours, then centrifuged to collect the product, and washed with water until neutral to obtain hollow carbon spheres.

[0048] (3) Ul...

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Abstract

The present invention relates to a carbon@Fe 2 o 3 @Carbon microsphere composites and their applications, the Carbon@Fe 2 o 3 The @carbon microsphere composite material is prepared from tetraethyl orthosilicate, ammonia water, resorcinol, formaldehyde, iron salt and dopamine, and the prepared carbon @Fe2O3@carbon microspheres have a diameter of 200-300 nm. The thickness of the microsphere carbon inner shell is about 15-30nm, and the Fe 2 o 3 The thickness of the middle layer is 30-60nm, the thickness of the carbon shell is 3-7nm; the carbon@Fe 2 o 3 @Carbon microsphere nanocomposites are used as anode materials for lithium-ion batteries. The advantage of the present invention is that: carbon@Fe of the present invention 2 o 3 @Carbon microsphere material is applied to lithium-ion batteries, which greatly improves the capacity retention rate of lithium batteries, and the process is simple, reproducible, and easy to implement.

Description

technical field [0001] The invention belongs to the technical field of negative electrode materials for lithium ion batteries, in particular to a carbon@Fe 2 o 3 @Carbon microsphere composites and their applications. Background technique [0002] Lithium-ion batteries have the advantages of high voltage, high capacity, small size, light weight, no memory effect, small self-discharge and long cycle life, making them a new chemical power source with great potential in the 21st century. At present, the theoretical capacity of the negative electrode material graphite in commercial lithium batteries is only 372mAh / g, which cannot meet the application requirements of high-performance batteries. Therefore, the development of anode materials with higher capacity, long cycle life and high rate performance has become the goal pursued by researchers at home and abroad. [0003] In order to increase the Fe 2 o 3 The electrochemical performance is mainly considered from the followin...

Claims

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Application Information

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Patent Type & AuthorityPatents(China)
IPC IPC(8): H01M4/36H01M4/525H01M4/62
CPCH01M4/625H01M4/364H01M4/525Y02E60/10
Inventor王震康杨宏训刘永闵曹宗林张翔王伟袁爱华
OwnerJIANGSU UNIV OF SCI & TECH