Hard carbon microspheres as well as preparation method and application thereof

A technology of carbon microspheres and hard carbon, applied in the field of hard carbon microspheres and its preparation, can solve the problems of complex preparation process, affecting the reversible capacity and cycle stability of hard carbon, and poor rate performance

Active Publication Date: 2022-02-15
张家港博威新能源材料研究所有限公司
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  • Summary
  • Abstract
  • Description
  • Claims
  • Application Information

AI Technical Summary

Benefits of technology

This patented technology allows creating tiny particles called carbons that are very small (1 um) on top of each other. These minute particles can be used alone or mixed together into larger ones like sandwich structures made up mostly layers of different materials. They also exhibit excellent properties such as high electrical conductivity and low reactance towards lithiation reactions during charging/dischargings cycles.

Problems solved by technology

This patents discuss various technical solutions related to reducing costs while maintaining or enhancing the benefits associated with traditional rechargeable batteries like LiCoO2. One solution involves developing new types of cathodes based on different principles including lower manufacturing complexity, less expensive starting materials, improved safety measures, reduced greenhouse gas emissions, and increased durability compared to current ones. Another approach focuses on forming closed cells within solidified carbons instead of hard shells.

Method used

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  • Hard carbon microspheres as well as preparation method and application thereof
  • Hard carbon microspheres as well as preparation method and application thereof
  • Hard carbon microspheres as well as preparation method and application thereof

Examples

Experimental program
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Embodiment 1

[0081] (1) Take 5g lignin, 10g mass fraction is 50% phenolic resin aqueous solution, be mixed with massfraction and be 15% aqueous solution (the total mass of lignin and phenolic resin accounts for 15% of aqueous solution gross mass), and at room temperature Stir for 1h;

[0082] (2) Transfer the aqueous solution of step (1) to the spray drying equipment, when the air inlet temperature is 150°C, the air outlet temperature is 90°C, and the ring air volume is 100mL min -1 , the inflow volume is 200ml h -1 Under the conditions of spray drying, the precursor nanospheres are obtained;

[0083] (3) Place the precursor nano-microspheres in an inert atmosphere, transfer them to an alumina crucible, place it in the center of a tube-type resistance furnace, and continuously pass in argon gas for protection. Then increase the temperature from room temperature to 1400 °C at a heating rate of 2 °C / min, and carbonize at a constant temperature of 1400 °C for 1 h, then naturally cool to room

Embodiment 2

[0086] (1) take by weighing 3g lignin, 14g mass fraction is 50% phenolic resin aqueous solution, is mixed with the mass fraction and is 15% aqueous solution (the total mass of lignin and phenolic resin accounts for 15% of aqueous solution gross mass), and at room temperature Stir for 3h;

[0087] (2) Transfer the aqueous solution of step (1) to the spray drying equipment, when the air inlet temperature is 140°C, the air outlet temperature is 90°C, and the ring air volume is 150mL min -1 , the inflow volume is 300ml h -1 Under the conditions of spray drying, the precursor nanospheres are obtained;

[0088] (3) Place the precursor nano-microspheres in an inert atmosphere, transfer them to an alumina crucible, place it in the center of a tube-type resistance furnace, and continuously pass in argon gas for protection. Then increase the temperature from room temperature to 1400 °C at a rate of 2 °C / min, and carbonize at a constant temperature of 1400 °C for 2 hours, then naturally

Embodiment 3

[0091] (1) take by weighing 7g lignin, 6g mass fraction is 50% phenolic resin aqueous solution, is mixed with the mass fraction and is 15% aqueous solution (the total mass of lignin and phenolic resin accounts for 15% of aqueous solution gross mass), and at room temperature Stir for 1h;

[0092] (2) Transfer the aqueous solution of step (1) to the spray drying equipment, when the air inlet temperature is 130°C, the air outlet temperature is 80°C, and the ring air volume is 200mL min -1 , the inflow volume is 250ml h -1 Under the conditions of spray drying, the precursor nanospheres are obtained;

[0093] (3) Place the precursor nano-microspheres in an inert atmosphere, transfer them to an alumina crucible, place it in the center of a tube-type resistance furnace, and continuously pass in argon gas for protection. Then increase the temperature from room temperature to 1400 °C at a rate of 2 °C / min, and carbonize at a constant temperature of 1400 °C for 3 hours, then naturally

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Abstract

The invention provides hard carbon microspheres as well as a preparation method and application thereof. In order to solve the problems of low initial coulombic efficiency and poor rate capability of the existing hard carbon negative electrode material for secondary batteries, the invention provides novel hard carbon microspheres which are obtained by co-carbonizing at least two hard carbon precursors, wherein the hard carbon precursors are two or more of water-soluble phenolic resin, glucose, cane sugar, starch and lignin. The hard carbon microspheres have better sphericity, larger interlayer spacing, extremely low specific surface area and excellent conductivity. The material is used for sodium ion batteries and has high reversible capacity, high initial coulombic efficiency and good rate capability. The preparation method is simple, the cost is low, the diameter range of the microspheres is controllable, and large-scale industrial production can be realized.

Description

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Claims

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Application Information

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Owner 张家港博威新能源材料研究所有限公司
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