期刊
ANGEWANDTE CHEMIE-INTERNATIONAL EDITION
卷 60, 期 10, 页码 5121-5124出版社
WILEY-V C H VERLAG GMBH
DOI: 10.1002/anie.202014323
关键词
carbon catalysts; oxygen reduction reaction; reaction mechanisms
资金
- JSPS KAKENHI [JP17H01342, 17F17345, 19K15356]
- Grants-in-Aid for Scientific Research [19K15356, 17F17345] Funding Source: KAKEN
The introduction of pyridinic nitrogen (pyri-N) into carbon-based electrocatalysts for the oxygen reduction reaction is considered to create new active sites. In this study, it was found that catalysts containing pyri-N molecules exhibited highest activity in acidic electrolytes, with 1,10-phenanthroline/CB showing the best performance.
The introduction of pyridinic nitrogen (pyri-N) into carbon-based electrocatalysts for the oxygen reduction reaction is considered to create new active sites. Herein, the role of pyri-N in such catalysts was investigated from a mechanistic viewpoint using carbon black (CB)-supported pyri-N-containing molecules as model catalysts; the highest activity was observed for 1,10-phenanthroline/CB. X-ray photoemission spectroscopy showed that in acidic electrolytes, both pyri-N atoms of 1,10-phenanthroline could be protonated to form pyridinium ions (pyri-NH+). In O-2-saturated electrolytes, one of the pyri-NH+ species was reduced to pyri-NH upon the application of a potential; no such reduction was observed in N-2-saturated electrolytes. This behavior was ascribed to electrochemical reduction of pyri-NH+ occurring simultaneously with the thermal adsorption of O-2, as supported by DFT calculations. According to these calculations, the coupled reduction was promoted by hydrophobic environments.
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