• 专利标题:   Method for preparing nano-lithium iron manganese positive electrode composite material, involves mixing iron source, manganese source, graphene oxide and additive and dispersing into water, followed by drying mixture, sintering and cooling.
  • 专利号:   CN109103452-A
  • 发明人:   ZHU W, LI L, ZHANG X, ZHU X, LIU D, ZHAO Y, WANG M, ZHAO S, CHENG C
  • 专利权人:   UNIV CHONGQING
  • 国际专利分类:   H01M004/58, H01M004/62
  • 专利详细信息:   CN109103452-A 28 Dec 2018 H01M-004/58 201917 Pages: 10 Chinese
  • 申请详细信息:   CN109103452-A CN10989274 28 Aug 2018
  • 优先权号:   CN10989274

▎ 摘  要

NOVELTY - A nano-lithium iron manganese positive electrode composite material preparing method involves mixing iron source, manganese source, graphene oxide and additive and dispersing into water to form a solution-A. The solution-A is dispersed in phosphorus source and water to form a solution-B. The solution-A and solution-B are mixed, added with nitric acid solution to regulate pH value of the reaction system to 2.0-4.5, and the reaction system is transferred into a hydrothermal reaction vessel at 150-180 degrees C for 10-24 hours, filtered, washed and dried to obtain manganese iron phosphorus/graphene. The manganese iron phosphorus/graphene, lithium source and carbon source are mixed to obtain mixture, where the lithium source and manganese iron phosphorus/graphene molar ratio is 1-1.05:1, the manganese iron phosphorus/graphene and carbon source molar ratio is 3-10:1. The mixture is dried and sintered at 600-800 degrees C for 4-12 hours, cooled and sieved to obtain the finished product. USE - Method for preparing nano-lithium iron manganese positive electrode composite material. ADVANTAGE - The method enables preparing nano-lithium iron manganese positive electrode composite material with uniform appearance, better dispersibility, shortened diffusion distance of lithium ion migration and enhanced ionic conductivity. DETAILED DESCRIPTION - A nano-lithium iron manganese positive electrode composite material preparing method involves mixing iron source, manganese source, graphene oxide and additive and dispersing into water to form a solution-A. The solution-A is dispersed in phosphorus source and water to form a solution-B. The solution-A and solution-B are mixed, added with nitric acid solution to regulate pH value of the reaction system to 2.0-4.5, and the reaction system is transferred into a hydrothermal reaction vessel at 150-180 degrees C for 10-24 hours, filtered, washed, dried and collected to obtain manganese iron phosphorus/graphene (Mn1-xFexPO4)/graphene. The manganese iron phosphorus/graphene, lithium source and carbon source are mixed to obtain mixture, where the lithium source and manganese iron phosphorus/graphene molar ratio is 1-1.05:1, and the manganese iron phosphorus/graphene and carbon source molar ratio is 3-10:1. The mixture is dried at 60-80 degrees C, sintered at 600-800 degrees C for 4-12 hours, cooled after crushing and subjected to sieving treatment to obtain the finished product.