• 专利标题:   Method for preparing metal-free oxygen reduction catalyst, involves washing glassy carbon substrate, immersing substrate in graphene oxide solution followed by utilizing carbon substrate and electrochemical reduction reaction.
  • 专利号:   CN104282920-A
  • 发明人:   HUANG D, SHEN Y, WANG M, ZHAN F, ZHANG B, ZHANG Y
  • 专利权人:   UNIV HUAZHONG SCI TECHNOLOGY
  • 国际专利分类:   H01M004/90
  • 专利详细信息:   CN104282920-A 14 Jan 2015 H01M-004/90 201526 Pages: 9 Chinese
  • 申请详细信息:   CN104282920-A CN10279097 04 Jul 2013
  • 优先权号:   CN10279097

▎ 摘  要

NOVELTY - A metal-free oxygen reduction catalyst preparing method involves washing glassy carbon substrate. The PDDA glassy carbon substrate having a surface layer is immersed in graphene oxide solution, after washing with water, dried to give the surface an oxide layer followed by repeating steps to give glassy carbon substrate, utilizing carbon substrate having multilayer phase resulting graphene oxide and PDDA as working electrode, molybdenum wire as the counter electrode, electrochemical reduction reaction in nitrogen-saturated phosphate buffer solution to give i.e. non-metal oxidation catalyst. USE - Method for preparing metal-free oxygen reduction catalyst. ADVANTAGE - The method enables preparing catalyst without need of high temperature device, in simple, convenient, and low energy consumption manner. DETAILED DESCRIPTION - A metal-free oxygen reduction catalyst preparing method involves washing glassy carbon substrate successively with 1.0-0.3 mu m alumina powder on the polishing cloth to polish mirror, as a working electrode, utilizing a molybdenum wire as the counter electrode, silver (Ag)/Ag+ as a reference electrode, performing electrochemical oxidation reaction in the electrolyte, the potential of the electrochemical oxidation reaction of 0-1.2V, to obtain negatively charged surface glassy carbon substrate, where the electrolyte solution is 4-aminobenzoic acid, lithium perchlorate and a mixture of absolute ethanol. The resulting glassy carbon substrate is immersed in 0.2-1 wt.% phthalate diethylene glycol diacrylate (PDDA), aqueous solution, for 5-60 minutes, removed and rinsed with water, dried with nitrogen to give a glassy carbon substrate having a surface with PDDA layer that is positively charged. The PDDA glassy carbon substrate having a surface layer is immersed in a 0.1-0.5mg ml-1 graphene oxide solution, for 5-60 minutes later, after washing with water, dried with nitrogen to give the surface an oxide layer having a graphene glassy carbon substrate, followed by repeating steps to give a glassy carbon substrate having a multi-layered graphene oxide and white PDDA, utilizing glassy carbon substrate having a multilayer phase resulting graphene oxide and PDDA as a working electrode, molybdenum wire as the counter electrode, Ag / AgCl as a reference electrode, the electrochemical reduction reaction in a nitrogen-saturated phosphate buffer solution to give glassy carbon substrate having a multi-phase electro-reduction of graphene oxide and PDDA, multi-phase power reduction of graphene oxide and PDDA, i.e. non-metal oxidation catalyst.