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Zinc-assisted MgO template synthesis of porous carbon-supported Fe-Nx sites for efficient oxygen reduction reaction catalysis in Zn-air batteries
Atomically dispersed iron-nitrogen-carbon catalysts offer great potential in oxygen reduction reaction (ORR), yet the poor exposure and low density of Fe-Nx sites causes relatively low ORR activity. Herein, a zinc-assisted MgO template strategy is reported to construct porous carbon-supported Fe-N4...
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Published in: | Applied catalysis. B, Environmental Environmental, 2022-09, Vol.313, p.121454, Article 121454 |
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Main Authors: | , , , , , , , , , , , , |
Format: | Article |
Language: | English |
Subjects: | |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | Atomically dispersed iron-nitrogen-carbon catalysts offer great potential in oxygen reduction reaction (ORR), yet the poor exposure and low density of Fe-Nx sites causes relatively low ORR activity. Herein, a zinc-assisted MgO template strategy is reported to construct porous carbon-supported Fe-N4 sites (Fe-N-C). Iron atoms surrounded by zinc species are converted to abundant Fe-N4 sites rather than Fe containing nanoparticles. Meanwhile, both the zinc species and the MgO template can effectively produce porous structure so as to increase the utilization of Fe-N4 sites. Fe-N-C achieves superior ORR performance and stability in alkaline medium. Theoretical calculations manifest that Fe-N4 sites can narrow the energy barrier for ORR. Moreover, finite element simulation exhibits the porous framework in Fe-N-C could significantly accelerate the diffusion of O2. Therefore, Fe-N-C provides a high peak power density and superior discharge ability toward Zn-air batteries.
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•Atomically dispersed Fe-N-C are prepared by zinc-assisted template strategy.•High density of Fe-Nx and hierarchical porosity boost oxygen reduction reaction.•The porous framework of Fe-N-C could significantly accelerate the diffusion of O2.•The catalyst exhibits an excellent performance in Zn-air batteries. |
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ISSN: | 0926-3373 1873-3883 |
DOI: | 10.1016/j.apcatb.2022.121454 |