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Engineering an iron atom-cluster nanostructure towards efficient and durable electrocatalysis
Iron-based catalysts have demonstrated fascinating activities in the oxygen reduction reaction (ORR), especially due to the synergistic effect between atoms and clusters, but challenging for further improvement. Herein, a strategy is developed to optimize the catalyst with nitrogen-coordinated Fe si...
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Published in: | Journal of materials chemistry. A, Materials for energy and sustainability Materials for energy and sustainability, 2023-04, Vol.11 (15), p.822-8212 |
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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: | Iron-based catalysts have demonstrated fascinating activities in the oxygen reduction reaction (ORR), especially due to the synergistic effect between atoms and clusters, but challenging for further improvement. Herein, a strategy is developed to optimize the catalyst with nitrogen-coordinated Fe single atoms (SAs) and closely surrounding Fe atomic clusters (ACs) towards efficient ORR. The Fe
SA
/Fe
AC
-NC 900 delivers excellent ORR activity with half-wave potential (
E
1/2
) in both acidic (0.80 V) and alkaline (0.90 V) media, as well as superior stability. Theoretical calculations further reveal that the synergistic effects of Fe-based SAs and ACs along with porous structures can decrease the overall energy barrier in the ORR process. Besides, the Fe
SA
/Fe
AC
-NC 900-based zinc-air battery manifests a high peak power density (214.3 mW cm
−2
) and a high-specific capacity (773.6 mA h g
−1
). This work provides a new perspective to highly optimize the synergistic interaction of SAs and ACs for boosting activity and energy storage.
The synergistic effect of Fe-based single-atoms and clusters in porous structures has significantly boosted the oxygen reduction reaction (ORR) activity, selectivity, and stability, as well as the application in energy storage. |
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ISSN: | 2050-7488 2050-7496 |
DOI: | 10.1039/d3ta00232b |