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A kind of siox-sic-c/g silicon-carbon composite material and its preparation and application

A technology of silicon-carbon composite materials and graphite materials, which is applied in the field of negative electrode materials and lithium-ion battery negative electrode materials, can solve problems such as poor conductivity, performance failure, and reduced rate performance, and achieve optimal structural stability and electrochemical performance. The effect of protecting the stability of the structure and improving the magnification performance

Active Publication Date: 2022-02-22
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, when the silicon negative electrode is applied to the lithium-ion battery system, there are the following problems: during the lithium intercalation process of the silicon negative electrode, a volume expansion of up to 300% will occur, and the material will be broken and pulverized during the repeated expansion and contraction process. , lose electrical contact with the collector liquid, and eventually lead to material failure; at the same time, the solid electrolyte film (SEI) formed during the first lithium intercalation process will rupture due to the volume change effect of silicon, and repeatedly form new ones on the exposed fresh silicon surface. The continuous thickening and increase of the SEI film will eventually lead to structural damage and performance failure of the silicon material; in addition, the low electronic conductivity and ionic conductivity of silicon itself also limit the capacity of the electrode and seriously reduce the rate performance.
However, for silicon oxide-based anodes with better cycle stability, there is still the problem of low reactivity due to poor conductivity during charge and discharge, and there is still a high volume expansion during electric cycles. , leading to side reactions between the material and the electrolyte, and rapid material failure, which seriously limits the practical application of the material.

Method used

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  • A kind of siox-sic-c/g silicon-carbon composite material and its preparation and application
  • A kind of siox-sic-c/g silicon-carbon composite material and its preparation and application
  • A kind of siox-sic-c/g silicon-carbon composite material and its preparation and application

Examples

Experimental program
Comparison scheme
Effect test

Embodiment 1

[0086] ①Mix 10g of waste graphite slag (particle size 10-15μm) and 0.5g of sodium hydroxide evenly, put it in an atmosphere furnace, and under the protection of argon atmosphere, raise the temperature to 750°C at 5°C / min, keep it for 2h, and naturally Cool to room temperature;

[0087] ②Dissolve the cooled material in 500ml of deionized water, after stirring, perform suction filtration, water washing, and dry in an oven at 100°C to obtain pretreated graphite;

[0088] 3. take by weighing 5g pretreatment graphite, 0.5g quartz sand (D50 particle diameter is 5~20% of pretreatment graphite), 2.5g asphalt, place in the granulator after mixing evenly and carry out secondary granulation, the obtained granule The particle size is 12~18μm;

[0089] ④ Add 1g of magnesium metal powder, mix the mixture evenly, put it in a reaction vessel, and raise the temperature to 650°C at 5°C / min in an argon atmosphere furnace, keep it warm for 2h, and cool down to room temperature naturally;

[009...

Embodiment 2

[0093] ① Mix 10g of waste graphite slag (particle size 10-15μm) and 1.5g of sodium hydroxide evenly, put it in an atmosphere furnace, and under the protection of argon atmosphere, raise the temperature to 800℃ at 5℃ / min, keep it warm for 2h, and let it Cool to room temperature;

[0094] ②Dissolve the cooled material in 500ml of deionized water, after stirring, perform suction filtration, water washing, and dry in an oven at 100°C to obtain pretreated graphite;

[0095] 3. take by weighing 5g pretreatment graphite, 1g silicon dioxide (D50 particle diameter is 5~20% of pretreatment graphite), 0.5g glucose, place in the granulator after mixing evenly and carry out secondary granulation, the obtained granule The particle size is 12~18μm;

[0096] ④ Add 0.8g of aluminum powder, mix the mixture evenly, place it in a reaction vessel, and raise the temperature to 550°C at 5°C / min in an argon atmosphere furnace, keep it warm for 2h, and cool down to room temperature naturally;

[009...

Embodiment 3

[0099] ① Mix 10g of waste graphite slag (particle size 10-15μm) and 1.5g of sodium hydroxide evenly, put it in an atmosphere furnace, and under the protection of argon atmosphere, raise the temperature to 800℃ at 5℃ / min, keep it warm for 2h, and let it Cool to room temperature;

[0100] ②Dissolve the cooled material in 500ml of deionized water, after stirring, perform suction filtration, water washing, and dry in an oven at 100°C to obtain pretreated graphite;

[0101] 3. take by weighing 5g pretreatment graphite, 5g silicon dioxide (D50 particle diameter is 5~20% of pretreatment graphite), 2g sucrose, place in the granulator after mixing evenly and carry out secondary granulation, the granule of gained granule The diameter is 12~18μm;

[0102] ④ Add 4g of magnesium powder, mix the mixture evenly, place it in a reaction vessel, and raise the temperature to 700°C at 5°C / min in an argon atmosphere furnace, keep it warm for 2 hours, and cool down to room temperature naturally; ...

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Abstract

The invention belongs to the field of lithium ion batteries, and specifically discloses a SiO x ‑SiC‑C / G silicon-carbon composite material, consisting of a graphite core and SiO coated layer by layer on the surface of the graphite core x layer, SiC layer and amorphous carbon layer; preferably, the particle size of the graphite core is 5-15 μm; coated in SiO x The total thickness of SiC layer, SiC layer and amorphous carbon layer is 1-5 μm. The invention also discloses the preparation and application of the material. The present invention provides a silicon-carbon composite material with a new structure, which uses graphite as the core, and the core is coated with SiO in situ x layer, on SiO x A SiC layer is in-situ coated on the layer, and an amorphous carbon layer is further in-situ coated on the surface of the SiC layer. The research of the present invention finds that the material with the special structure and morphology has better structural stability, better capacity and cycle stability.

Description

technical field [0001] The invention belongs to the technical field of negative electrode materials for lithium ion batteries, and in particular relates to a preparation method for negative electrode materials, in particular using waste carbon slag as a raw material. Background technique [0002] Fossil energy based on coal and oil can no longer meet the needs of sustainable development of human beings. It is imperative to improve the energy consumption structure and reduce dependence on fossil energy. As a green energy storage device at the forefront of technology, lithium-ion batteries have been widely used in portable electronic devices and electric vehicles. At the same time, these fields have also put forward higher and higher requirements for the energy density of energy storage devices. However, the current negative electrode materials for lithium-ion batteries are mainly graphite, which has the defect of low specific capacity, making it difficult to further increase ...

Claims

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Application Information

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IPC IPC(8): C01B32/21C01B32/05C01B32/97C01B33/113H01M4/36H01M4/48H01M4/587H01M4/62H01M10/0525H01M10/54
CPCC01B32/21C01B32/05C01B32/97C01B33/113H01M4/362H01M4/483H01M4/587H01M4/625H01M10/0525H01M10/54C01P2006/40C01P2002/72C01P2004/03C01P2004/61C01P2006/80Y02W30/84Y02E60/10
Inventor 周昊宸周向清王鹏周进辉
Owner 湖南宸宇富基新能源科技有限公司