Oxygen reduction reaction in a droplet on graphite: Direct evidence that the edge is more active than the basal plane

Anli Shen, Yuqin Zou, Qiang Wang, Robert A.W. Dryfe, Xiaobing Huang, Shuo Dou, Liming Dai, Shuangyin Wang

Research output: Contribution to journalArticlepeer-review

460 Scopus citations

Abstract

Carbon-based metal-free electrocatalysts for the oxygen reduction reaction (ORR) in alkaline medium have been extensively investigated with the aim of replacing the commercially available, but precious platinum-based catalysts. For the proper design of carbon-based metal-free electrocatalysts for the ORR, it would be interesting to identify the active sites of the electrocatalyst. The ORR was now studied with an air-saturated electrolyte solution droplet (diameter ca. 15 μm), which was deposited at a specified position either on the edge or on the basal plane of highly oriented pyrolytic graphite. Electrochemical measurements suggest that the edge carbon atoms are more active than the basal-plane ones for the ORR. This provides a direct way to identify the active sites of carbon materials for the ORR. Ball-milled graphite and carbon nanotubes with more exposed edges were also prepared and showed significantly enhanced ORR activity. DFT calculations elucidated the mechanism by which the charged edge carbon atoms result in the higher ORR activity. On the cutting edge: To study the oxygen reduction reaction (ORR), an air-saturated electrolyte solution droplet with a diameter of approximately 15 μm was deposited at a specified position on the edge (see picture) or on the basal plane of highly oriented pyrolytic graphite. Electrochemical measurements suggest that the edge sites are catalytically more active than basal-plane sites towards the ORR.

Original languageEnglish
Pages (from-to)10804-10808
Number of pages5
JournalAngewandte Chemie - International Edition
Volume53
Issue number40
DOIs
StatePublished - 26 Sep 2014

Keywords

  • droplets
  • electrochemistry
  • fuel cell
  • graphite
  • oxygen reduction reaction

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