• 专利标题:   Preparing lithium ion battery silicon cathode material, involves removing metal impurities from serpentine, filter pressing by concentrated sulfuric acid, sintering, adding obtained amorphous silicon into solvent, adding graphene oxide slurry, sintering and adding sintered particles to graphene.
  • 专利号:   CN113571685-A, CN113571685-B
  • 发明人:   ZHU W, LIN Y
  • 专利权人:   XINHUA SHANGHAI EQUIP CO LTD
  • 国际专利分类:   H01M010/0525, H01M004/62, H01M004/38
  • 专利详细信息:   CN113571685-A 29 Oct 2021 H01M-004/38 202202 Chinese
  • 申请详细信息:   CN113571685-A CN10652114 11 Jun 2021
  • 优先权号:   CN10652114

▎ 摘  要

NOVELTY - The preparation of a lithium ion battery silicon negative electrode material involves: crushing serpentine, removing metal impurities, acid washing and filter pressing on the crushed serpentine by adopting 98 mass% concentrated sulfuric acid to obtain filter residue, and sintering the filter residue at 900-1100?oC to obtain amorphous silicon; adding amorphous silicon into a dispersion solvent to obtain amorphous silicon slurry, adding graphene oxide slurry and dispersing for 30 minutes to obtain composite slurry; heating the composite slurry to 200?oC, emulsifying for 2 hours, and spray drying the emulsified slurry to obtain particles with the particle size less than 30 microns; sintering the particles at 1000?oC under argon and zero pressure; adding the sintered particles into N-methyl-2-pyrrolidone solution, dispersing for 30 minutes, and adding graphene and carbon nano tubes; spray drying the dispersed slurry, sieving and vacuum packaging. USE - Preparation method of high performance lithium ion battery silicon cathode material. ADVANTAGE - The method uses serpentine as the source material of silicon. The serpentine has a large reserve, and is easy to buy and low cost. The method provides the high performance lithium ion battery silicon cathode material with excellent electrochemical performance, capacity of 2800 mAh/g under the condition that the charging and discharging rate of 0.5C, the first effect of more than 80%, and the cycle performance in 200 weeks of more than 75%. The preparation process is simple and industrial large-scale mass production can be achieved.