Cobalt single atoms loading on carbon black for efficient hydrogen peroxide production
The production of hydrogen peroxide (H 2 O 2 ) by 2-electron oxygen reduction reaction (ORR) in acidic electrolytes is a promising alternative to the existing anthraquinone process. However, the development of cost-effective catalysts with high activity for H 2 O 2 electrosynthesis remains a great c...
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Veröffentlicht in: | Ionics 2024-03, Vol.30 (3), p.1773-1783 |
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Hauptverfasser: | , , , , , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | The production of hydrogen peroxide (H
2
O
2
) by 2-electron oxygen reduction reaction (ORR) in acidic electrolytes is a promising alternative to the existing anthraquinone process. However, the development of cost-effective catalysts with high activity for H
2
O
2
electrosynthesis remains a great challenge. Here, we report a cobalt-nitrogen-carbon catalyst in which cobalt single atoms are supported on carbon black (Co-N-CB) for the electrosynthesis of H
2
O
2
in an acid medium. The prepared Co-N-CB shows high activity for O
2
reduction into H
2
O
2
with an average selectivity of 80.6% over a wide potential range of 0.1–0.7 V vs. RHE in 0.1 M HClO
4
electrolytes. We found that (i) the Co single atoms are the active sites of 2-electron ORR; (ii) a catalyst for efficient H
2
O
2
production by O
2
reduction should achieve a good balance between high ORR activity and H
2
O
2
selectivity. Using Co-N-CB as a cathodic catalyst, the electrochemical device could electrosynthesize H
2
O
2
directly from H
2
and O
2
with a high productivity of 291.0 mol kg
cat
−1
h
−1
. Our work provides a flexible way to prepare affordable catalysts for efficient H
2
O
2
electrosynthesis. |
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ISSN: | 0947-7047 1862-0760 |
DOI: | 10.1007/s11581-023-05357-5 |