Controllable synthesis of Fe–N4 species for acidic oxygen reduction
Controllable design and synthesis of catalysts with the target active sites are extremely important for their applications such as for the oxygen reduction reaction (ORR) in fuel cells. However, the controllably synthesizing electrocatalysts with a single type of active site still remains a grand ch...
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Veröffentlicht in: | Carbon energy 2020-09, Vol.2 (3), p.452-460 |
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Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Controllable design and synthesis of catalysts with the target active sites are extremely important for their applications such as for the oxygen reduction reaction (ORR) in fuel cells. However, the controllably synthesizing electrocatalysts with a single type of active site still remains a grand challenge. In this study, we developed a facile and scalable method for fabricating highly efficient ORR electrocatalysts with sole atomic Fe–N4 species as the active site. Herein, the use of cost‐effective highly porous carbon as the support not only could avoid the aggregation of the atomic Fe species but also a feasible approach to reduce the catalyst cost. The obtained atomic Fe–N4 in activated carbon (aFe@AC) shows excellent ORR activity. Its half‐wave potential is 59 mV more negative but 47 mV more positive than that of the commercial Pt/C in acidic and alkaline electrolytes, respectively. The full cell performance test results show that the aFe@AC sample is a promising candidate for direct methanol fuel cells. This study provides a general method to prepare catalysts with a certain type of active site and definite numbers.
A controllable and scalable strategy is used for fabricating oxygen reduction reaction (ORR) catalysts with a single type of atomic Fe–N4 species as the active site for fuel cell applications. The resulting catalyst aFe@AC exhibits superior ORR activity in both acidic and alkaline solutions. This study provides a practical method of fabricating electrocatalysts with the target active sites for high‐performance catalysis. |
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ISSN: | 2637-9368 2637-9368 |
DOI: | 10.1002/cey2.47 |