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Boron-phosphorus co-doped porous silicon negative electrode material and preparation method thereof

A negative electrode material and co-doping technology, applied in the direction of chemical instruments and methods, nanotechnology for materials and surface science, silicon oxide, etc., can solve the problem of ensuring uniform dispersion of different components in composite materials and reducing porous silicon Electrochemical performance, increasing the difficulty of preparation and other issues, to improve the comprehensive electrochemical performance, good practical prospects, and solve the effect of volume expansion

Active Publication Date: 2020-02-25
湖南宸宇富基新能源科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Problems solved by technology

However, although the initial reaction temperature of magnesia thermal reduction is low, the magnesia thermal reduction process is a violent exothermic reaction process. The local temperature in the reaction system is too high, which leads to partial melting and agglomeration of silicon. The accumulation will lead to the collapse and agglomeration of the porous structure formed by the magnesia thermal reaction, thereby reducing the electrochemical performance of porous silicon; in addition, in order to improve the conductivity of porous silicon and enhance the lithium storage performance of porous silicon, it is often used before or after the magnesia thermal reduction process. Additional compounding or cladding processes are required to mix high-conductivity or high-stability materials such as carbon materials, ceramic materials, metal materials, etc., with silicon. These additional compounding or cladding processes greatly increase the difficulty of preparation and are difficult Guarantees uniform dispersion of the different components in the composite

Method used

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  • Boron-phosphorus co-doped porous silicon negative electrode material and preparation method thereof
  • Boron-phosphorus co-doped porous silicon negative electrode material and preparation method thereof
  • Boron-phosphorus co-doped porous silicon negative electrode material and preparation method thereof

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0029] Take boric acid, phosphoric acid and ethyl orthosilicate according to the mass ratio of the elements boron, phosphorus and silicon in the compound as 5:25:100, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add 0.06 with a relative total volume of 0.4 mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:2:3 to obtain solution B; Quickly pour solution A into solution B at a ratio of 1:1, stir at room temperature for 3 hours, let stand for 12 hours, and finally wash the obtained precipitate repeatedly with ethanol and water, separate and dry the obtained powder in an air atmosphere at 550°C After calcination for 2 hours, the silicon dioxide precursor can be obtained.

[0030] Take 1g of the above-mentioned silica precursor, grind it with 1g of magnesium p...

Embodiment 2

[0035] According to the mass ratio of the elements boron, phosphorus and silicon in the compound is 2.5:12.5:100, take boric acid, phosphoric acid and ethyl orthosilicate, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add 0.06 with a relative total volume of 0.8 mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:1:1 to obtain solution B; Quickly pour solution A into solution B at a ratio of 1:1, stir at room temperature for 3 hours, let stand for 12 hours, and finally wash the obtained precipitate repeatedly with ethanol and water, separate and dry the obtained powder in an air atmosphere at 400°C Calcined for 6 hours, the silicon dioxide precursor can be obtained.

[0036] Take 1g of the above-mentioned silica precursor, grind it with 1g of magnesium powde...

Embodiment 3

[0041] Take sodium borate, ammonium dihydrogen phosphate and sodium silicate according to the mass ratio of boron, phosphorus and silicon in the compound as 5:25:100, dissolve them in 10 times the volume of ethanol, stir evenly for 10 minutes, and then add the relative total volume of 0.8 The 0.1mol / L hydrochloric acid solution was uniformly stirred at 60°C for 3 hours and then cooled to room temperature to obtain solution A; then ammonia water, deionized water, and absolute ethanol were uniformly mixed at a volume ratio of 1:5:5 to obtain solution B; The volume ratio is 1:1, quickly pour solution A into solution B, stir at room temperature for 3 hours, and let it stand for 12 hours. Finally, the obtained precipitate is repeatedly washed with ethanol and water, and the powder obtained after separation and drying is air-conditioned at 700°C. The silicon dioxide precursor can be obtained by calcining in the atmosphere for 1 h.

[0042] Take 1g of the above-mentioned silica precu...

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Abstract

The invention discloses a boron-phosphorus co-doped porous silicon negative electrode material and a preparation method thereof. The boron-phosphorus co-doped porous silicon negative electrode material is characterized in that the material takes elemental silicon as a matrix and is doped with boron atoms and phosphorus atoms, the mass doping amount of the boron atoms is 0.001-0.17 wt%, the mass doping amount of the phosphorus atoms is 0.01-2wt%, and the balance is elemental silicon; and the structure of the silicon material is a hollow porous structure. The silicon source and the doping sourceare both soluble liquid precursors, the uniform doping characteristic of the product silicon material can be guaranteed, and the doping content can be adjusted in a large range by changing the proportion of the added raw materials. Silicon reduction and element doping processes are synchronously completed by adopting a magnesiothermic reduction method, an additional compounding or coating step isnot needed, the energy consumption is low, the process is simple, and the method is suitable for industrial production. Two important problems of volume expansion and poor conductivity of the siliconmaterial in industrial production are solved at the same time, and the obtained product has excellent comprehensive performance and good practical prospect.

Description

technical field [0001] The invention belongs to the field of inorganic nano-energy storage materials, and in particular relates to a boron-phosphorus co-doped porous silicon negative electrode material and a preparation method thereof. Background technique [0002] With the continuous development of society, people's demand for energy continues to increase, traditional fossil fuels are gradually exhausted, and the timeliness of new energy sources such as wind energy and solar energy is greatly limited, so the demand for energy storage devices is increasing; At the same time, the rapid development of electric vehicles and smart grids puts higher demands on high energy density energy storage devices. In this context, lithium-ion batteries, as an electrochemical energy storage device with obvious advantages, have attracted extensive attention. Traditional graphite anode materials due to their low lithium storage capacity (372mAh g -1 ) is difficult to meet the current needs, ...

Claims

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Application Information

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Patent Type & Authority Applications(China)
IPC IPC(8): H01M4/38C01B33/12C01B33/023B82Y30/00H01M10/0525
CPCH01M4/386C01B33/023C01B33/12B82Y30/00H01M10/0525Y02E60/10
Inventor 杨娟唐晶晶周向阳张佳明任永鹏周昊宸王鹏胡挺杰
Owner 湖南宸宇富基新能源科技有限公司