• 专利标题:   Preparing double oxide/graphene nanocomposite electrode material comprises e.g. dissolving cobalt chloride hexahydrate and aluminum nitrate nonahydrate in small beaker containing distilled water, drying and calcining.
  • 专利号:   CN107403700-A, CN107403700-B
  • 发明人:   SONG J, QIN P, NIU H, MAO C, CHEN J
  • 专利权人:   UNIV ANHUI, UNIV ANHUI
  • 国际专利分类:   B82Y040/00, H01G011/30, H01G011/36, H01G011/46, H01G011/86
  • 专利详细信息:   CN107403700-A 28 Nov 2017 H01G-011/86 201805 Pages: 10 Chinese
  • 申请详细信息:   CN107403700-A CN10601519 21 Jul 2017
  • 优先权号:   CN10601519

▎ 摘  要

NOVELTY - Preparing double oxide/graphene nanocomposite electrode material comprises e.g. dissolving cobalt chloride hexahydrate and aluminum nitrate nonahydrate in a small beaker containing distilled water and continue adding graphene (2.6 mg/ml), adding 2 ml aquoeus ammonia, removing magnet, transferring mixed solution into volume of 50 ml stainless steel autoclave containing polytetrafluoroethylene liner, sealing in high-pressure reactor, placing in oven at 180 degrees C, washing with distilled water and ethanol, placing precipitate in oven at 60 degrees , drying and calcining. USE - The method is useful for preparing double oxide/graphene nanocomposite electrode material (claimed). ADVANTAGE - The method has high yield, simple preparation process and is suitable for industrial production; and product has specific volume of 968 F/g at scanning current density of 1 A/g, and retention rate remains as high as 85% after 1000 cycles. DETAILED DESCRIPTION - Preparing double oxide/graphene nanocomposite electrode material comprises dissolving 1.19 g cobalt chloride hexahydrate and 0.075 g aluminum nitrate nonahydrate in a small beaker containing 30 ml distilled water and continue adding 4 ml graphene (2.6 mg/ml), sonicating for 30 minutes, stirring with magnetic stirrer, adding 2 ml aquoeus ammonia, removing magnet, transferring mixed solution into volume of 50 ml stainless steel autoclave containing polytetrafluoroethylene liner, sealing in high-pressure reactor, placing in oven at 180 degrees C, removing for 12 hours and allowing to cool to room temperature, centrifugating at 8000 revolution per minute for 5 minutes to obtain precipitate, washing three times with distilled water and ethanol, placing precipitate in oven at 60 degrees , drying for 12 hours, calcining for 3 hours to obtain final product.