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Ferric oxide nano material, preparation method of ferric oxide nano material, lithium ion battery negative pole and lithium ion battery

A ferric oxide and lithium ion battery technology, applied in the field of nanomaterials, can solve the problems of ferric oxide reversible cycle capacity attenuation, low storage capacity of graphite lithium, excessively long dendrite piercing, etc. Denaturation, good product quality effect

Active Publication Date: 2016-10-12
ANHUI NORMAL UNIV
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

[0003] At present, most of the negative electrode materials of lithium-ion batteries use graphitized carbon materials, and the lithium storage capacity of graphite is relatively low, only 370mAhg -1 , it is easy to cause the decomposition of the electrolyte and the precipitation of dendrite lithium when lithium is intercalated. The dendrite is too long to pierce the separator, resulting in a short circuit of the battery, which leads to a series of safety problems.
[0004] Ferric oxide (Fe 2 o 3 ) is an n-type semiconductor oxide (Eg=2.2eV), which is a functional material with many uses, especially when it is used as a negative electrode material for lithium-ion batteries, it has a capacity of up to 1007mAhg -1 Theoretical capacity, at the same time because of its low cost, easy large-scale production, and non-toxic and non-polluting advantages, it is regarded as a very potential new generation of lithium-ion battery electrode materials, but due to the accompanying lithium intercalation and delithiation reactions The huge volume expansion and contraction, as well as the separation of the active material and the current collector, make the reversible cycle capacity of ferric oxide decay quickly

Method used

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  • Ferric oxide nano material, preparation method of ferric oxide nano material, lithium ion battery negative pole and lithium ion battery
  • Ferric oxide nano material, preparation method of ferric oxide nano material, lithium ion battery negative pole and lithium ion battery
  • Ferric oxide nano material, preparation method of ferric oxide nano material, lithium ion battery negative pole and lithium ion battery

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Experimental program
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Effect test

Embodiment 1

[0048]1. Mixing process: Dissolve 0.1g of ferrous sulfate heptahydrate in a mixed solution of 16mL of ethylene glycol and 8mL of distilled water, then add 20 microliters of hydrazine hydrate solution with a mass fraction of 50% as an antioxidant to obtain a green solution, marked It is solution a; dissolve 0.046g and 0.02g of oxalic acid and sodium hydroxide in a mixed solution of 16mL ethylene glycol and 8mL distilled water successively, and mark it as solution b. After placing the above two solutions of a and b in a water bath at 30°C for 2 minutes, quickly pour the solution of a into the solution of b in a 30°C oven with stirring, and continue to stir for 2 minutes to obtain a light yellow turbid solution. The cloudy solution was left to age at 30°C for 12 hours, and then the precipitate was filtered, washed, and vacuum-dried at 30°C for 12 hours to obtain light yellow ferrous oxalate dihydrate precursor powder.

[0049] 2. Transformation process: Disperse 0.1g of ferrous o...

Embodiment 2

[0052] 1. Mixing process: Dissolve 0.5g of ferrous sulfate heptahydrate in a mixed solution of 16mL of ethylene glycol and 8mL of distilled water, then add 25 microliters of hydrazine hydrate solution with a mass fraction of 50% as an antioxidant to obtain a green solution, marked Liquid b; 0.23 g and 0.1 g of oxalic acid and sodium hydroxide were successively dissolved in a mixed solution of 16 mL of ethylene glycol and 8 mL of distilled water, and marked as liquid a. After placing the above two solutions of a and b in a water bath at 50°C for 10 minutes, quickly pour liquid b into liquid a under the condition of stirring in an oven at 50°C, and continue stirring for 5 minutes to obtain a light yellow turbid solution. The cloudy solution was left to age at 50°C for 8 hours, and then the precipitate was filtered, washed, and vacuum-dried at 50°C for 8 hours to obtain light yellow ferrous oxalate dihydrate precursor powder.

[0053] 2. Transformation process: Disperse 0.1g of f...

Embodiment 3

[0056] 1. Mixing process: Dissolve 1.5g of ferrous sulfate heptahydrate in a mixed solution of 32mL of ethylene glycol and 10mL of distilled water, and then add 35 microliters of hydrazine hydrate as an antioxidant to obtain a green solution, which is marked as liquid b; 0.8g and 0.5g of oxalic acid and sodium hydroxide were successively dissolved in a mixed solution of 32mL of ethylene glycol and 10mL of distilled water, marked as liquid a. After placing the above two solutions of a and b in a water bath at 60°C for 10 minutes, quickly pour liquid b into liquid a under the condition of stirring in an oven at 60°C, and continue stirring for 5 minutes to obtain a light yellow turbid solution. The cloudy solution was left to age at 70°C for 4 hours, and then the precipitate was filtered, washed, and vacuum-dried at 70°C for 6 hours to obtain light yellow ferrous oxalate dihydrate precursor powder.

[0057] 2. Conversion process: Disperse 0.2 g of ferrous oxalate dihydrate precur...

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Abstract

The invention relates to a ferric oxide nano material, a preparation method of the ferric oxide nano material, a lithium ion battery negative pole and a lithium ion battery. The ferric oxide nano material comprises micro-nano tubes formed by assembling ferric oxide nanosheets, wherein the specific surface area of the ferric oxide nano material is 75.3-126.2 m<2>.g <-1>, the outer diameter of each micro-nano tube is 700-900 nm, the inner diameter of each micro-nano tube is 300-500 nm, and each micro-nano tube is 4.0-10.0 mu m long. The preparation method comprises steps as follows: mixing, conversion and calcination. The prepared Fe2O3 product in a micro-nano tube shape is red powder and has high purity and good quality. The micro-nano tubes formed by assembling the ferric oxide nanosheets have relatively large specific surface areas, and the material serving as a lithium battery negative pole material is fully contacted with an electrolyte, can remarkably relieve volume expansion and contraction in lithium intercalation and deintercalation processes and has relatively large specific capacity and better cycle performance.

Description

technical field [0001] The invention belongs to the technical field of nanometer materials, and in particular relates to a nanometer material of ferric oxide and a preparation method thereof, a negative electrode of a lithium ion battery and a lithium ion battery. Background technique [0002] Lithium-ion batteries are famous for their outstanding advantages such as high working voltage (3.7V), high specific energy, low self-discharge rate, no memory effect, long cycle life, good storage performance, wide temperature range, relative safety, reliability and environmental friendliness. It has been widely favored in the field of new energy. [0003] At present, most of the negative electrode materials of lithium-ion batteries use graphitized carbon materials, and the lithium storage capacity of graphite is relatively low, only 370mAhg -1 , It is easy to cause the decomposition of the electrolyte and the precipitation of dendrite lithium when lithium is intercalated. The dendri...

Claims

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Application Information

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IPC IPC(8): H01M4/52H01M10/0525C01G49/06B82Y30/00B82Y40/00
CPCB82Y30/00B82Y40/00C01G49/06H01M4/523H01M10/0525Y02E60/10
Inventor 黄家锐张思敏陈玉翟慕衡
Owner ANHUI NORMAL UNIV
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