Affiliation:
1. The Key Laboratory of Fuel Cell Technology of Guangdong Province & The Key Laboratory of New Energy School of Chemistry and Chemical Engineering South China University of Technology Guangzhou 510641 China
2. Centre Énergie, Matériaux et Télécommunications Institute National de la Recherche Scientifique Varennes Québec J3X 1P7 Canada
3. Dalian National Laboratory for Clean Energy (DNL) Dalian Institute of Chemical Physics Chinese Academy of Sciences Dalian 116023 P. R. China
4. School of Chemistry and Chemical Engineering Dalian University of Technology Dalian 116024 China
Abstract
AbstractSingle‐atom metal‐doped M–N–C (M═Fe, Co, Mn, or Ni) catalysts exhibit excellent catalytic activity toward oxygen reduction reactions (ORR). However, their performance still has a large gap considering the demand for their practical applications. This study reports a high‐performance dual single‐atom doped carbon catalyst (HfCo–N–C), which is prepared by pyrolyzing Co and Hf co‐doped ZIF‐8 . Co and Hf are atomically dispersed in the carbon framework and coordinated with N to form Co–N4 and Hf–N4 active moieties. The synergetic effect between Co–N4 and Hf–N4 significantly enhance the catalytic activity and durability of the catalyst. In an acidic medium, the ORR half‐wave potential (E1/2) of the catalyst is up to 0.82 V , which is much higher than that of the Co–N–C catalyst without Hf co‐doping (0.80 V). The kinetic current density of the catalyst is up to 2.49 A cm−2 at 0.85 V , which is 1.74 times that of the Co–N–C catalyst without Hf co‐doping. Moreover, the catalyst exhibits excellent cathodic performance in single proton exchange membrane fuel cells and Zn–air batteries. Furthermore, Hf co‐doping can effectively suppress the formation of H2O2, resulting in significantly improved stability and durability.
Funder
National Natural Science Foundation of China
National Key Research and Development Program of China
Cited by
3 articles.
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