A preparation method of silicon-carbon negative electrode material for lithium ion battery

A lithium-ion battery and negative electrode material technology, which is applied to battery electrodes, circuits, electrical components, etc., can solve problems such as cycle performance attenuation, low conductivity, and low lithium intercalation potential

Inactive Publication Date: 2019-01-15
江西中汽瑞华新能源科技有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

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Problems solved by technology

As we all know, the negative electrode of traditional lithium-ion batteries mainly uses graphite, and its theoretical specific capacity is only 372mAh / g, which is difficult to meet the needs of today's social development. However, silicon (Si) has a high specific capacity, and lithium ions and Si are alloyed to form Si 22 Li 5 , the theoretical specific capacity can be as high as 4200mAh / g, and has a low lithium intercalation potential, which is a very potential lithium ion negative electrode material
However, Si also has its own disadvantages. Si is a semiconductor material with low intrinsic conductivity (10 -5 ~10 -3 S / cm), the lithium ion diffusion coefficient is low (10 -14 ~10 -13 cm 2 / s), and during the charge-discharge cycle, the insertion and extraction of lithium ions will cause the Si negative electrode to expand and shrink by more than 300%, and the mechanical stress generated will gradually pulverize the Si material, and the newly exposed Si surface New SEI films are continuously formed, causing irreversible loss of lithium ions, collapse of the structure, and eventually falling off from the current collector, resulting in rapid degradation of cycle performance

Method used

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  • A preparation method of silicon-carbon negative electrode material for lithium ion battery
  • A preparation method of silicon-carbon negative electrode material for lithium ion battery
  • A preparation method of silicon-carbon negative electrode material for lithium ion battery

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Embodiment 1

[0030] A method for preparing a silicon-carbon negative electrode material for a lithium-ion battery, the specific preparation steps are as follows:

[0031] The first step, 1g mean particle diameter is the nano Si powder of 100nm, 0.03g hexadecyl trimethylammonium bromide, 23.8g Zn(NO 3 ) 2 ·6H 2 O, 6.6g H 2 BDC and 1g of CNTs were added to 800mL of DMF, and ultrasonically stirred at 40KHz for 15min to form a uniformly dispersed nano-Si / CNTs suspension;

[0032] In the second step, 32g of TEA was added dropwise to the suspension at a constant speed. After sufficient reaction, the precipitate was washed and filtered with DMF three times, and then placed in a vacuum oven at 150°C for 18 hours to obtain the precursor complex;

[0033] In the third step, the obtained precursor is placed in a tube furnace with an argon atmosphere, the flow rate of the argon gas is 60mL / min, heated to 900°C at a heating rate of 5°C / min and kept for 3 hours, then cooled to room temperature with t...

Embodiment 2

[0036] A method for preparing a silicon-carbon negative electrode material for a lithium-ion battery, the specific preparation steps are as follows:

[0037] The first step, 1g average particle diameter is the nano silicon powder of 150nm, 0.04g polyvinylpyrrolidone, 11.9g Zn(NO 3 ) 2 ·6H 2 O, 3.3 g H 2 BDC and 1g of CNTs were added to 400mL of DMF, and ultrasonically stirred at an ultrasonic frequency of 30KHz for 20min to form a uniformly dispersed nano-Si / CNTs suspension;

[0038] In the second step, 16g of TEA was added dropwise to the suspension at a constant speed. After sufficient reaction, the precipitate was washed and filtered with DMF four times, and then placed in a vacuum oven at 140°C for 24 hours to obtain the precursor complex;

[0039] The third step is to place the obtained precursor in a tube furnace with a nitrogen atmosphere. The flow rate of nitrogen gas is 50mL / min. After heating to 950°C at a heating rate of 10°C / min and keeping it for 2 hours, it is...

Embodiment 3

[0042] The first step, 1g average particle diameter is the nano-Si powder of 200nm, 0.02g p-ethylbenzoic acid, 35.7g Zn(NO 3 ) 2 ·6H 2 O, 9.9 g H 2 BDC and 1g of CNTs were added to 1200mL of DMF, and ultrasonically stirred at 50KHz for 10min to form a uniformly dispersed nano-Si / CNTs suspension;

[0043] In the second step, 48g of TEA was added dropwise to the suspension at a constant speed. After sufficient reaction, the precipitate was washed and filtered with DMF three times, and then placed in a vacuum oven at 160°C for 14 hours to obtain the precursor complex;

[0044] In the third step, the obtained precursor is placed in a tube furnace with a nitrogen atmosphere, the nitrogen gas flow rate is 80mL / min, heated to 850°C at a heating rate of 2°C / min and kept for 4 hours, then cooled to room temperature with the furnace to obtain silicon carbon composite materials;

[0045] The fourth step is to uniformly mix the silicon-carbon composite material accounting for 40% of t...

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Abstract

The invention discloses a preparation method of a silicon-carbon negative electrode material of a lithium ion battery, comprising the following steps: adding a proper amount of nano-silicon powder, adispersant, zinc nitrate hexahydrate, terephthalic acid and CNTs to a sufficient amount of N, N- A mixed solution is prepared from dimethylformamide, and then the mixed solution is uniformly dispersed; A suitable amount of triethylamine reagent is slowly and uniformly adde into that mixture prepared in the first step, aft full reaction, the precipitate is washed, filtered and dried to obtain CNTs / MOF- 5, coat that nano Si precursor; The precursor was put into a tubular furnace protected by inert gas and carbonized at high temperature to obtain silicon-carbon composites. Silicon-carbon anode materials for lithium ion batteries were prepared by mixing the prepared silicon-carbon composite and artificial graphite homogeneously. CNTs is adde into that preparation process of the silicon-carbonnegative electrode material of the lithium ion battery, and the CNTs can be use as a conductive network structure, the electronic conductivity of the silicon-carbon negative electrode is greatly improved, and the first effect and the multiplicity of the charge-discharge cycle of the silicon-carbon negative electrode are improved.

Description

technical field [0001] The invention belongs to the field of lithium-ion batteries, and relates to a preparation method of a silicon-carbon negative electrode material of a lithium-ion battery. Background technique [0002] At the end of the 20th century, with the development of portable consumer electronics (mobile phones, video cameras, portable computers), the field of batteries has received a new impact, and batteries with high energy density are urgently needed to meet market demand. However, lead-acid batteries were not suitable for these applications, and attention was turned to nickel-cadmium batteries, but were eventually surpassed by lithium-ion batteries (LIB) in the early 1990s. As part of our everyday life, LIBs have been continuously improved over the past 25 years and have received a great deal of research attention. [0003] Today LIBs also play a vital role in many fields from electric vehicles to energy storage for alternative energy sources (solar, wind, ...

Claims

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Application Information

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IPC IPC(8): H01M4/38H01M4/62
CPCH01M4/386H01M4/625Y02E60/10
Inventor 张小溪陈伟王海文范进雷
Owner 江西中汽瑞华新能源科技有限公司
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