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Constructing a CoO–CuO x heterostructure for efficient electrochemical reduction of nitrate to ammonia
The electrochemical nitrate reduction reaction (NtrRR) represents a sustainable approach to realize the green synthesis of ammonia, yet developing efficient electrocatalysts to improve the sluggish reaction kinetics and the undesirable selectivity towards NH 3 , while simultaneously suppressing the...
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Published in: | Sustainable energy & fuels 2023-10, Vol.7 (20), p.5039-5045 |
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Main Authors: | , , , , |
Format: | Article |
Language: | English |
Citations: | Items that this one cites Items that cite this one |
Online Access: | Get full text |
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Summary: | The electrochemical nitrate reduction reaction (NtrRR) represents a sustainable approach to realize the green synthesis of ammonia, yet developing efficient electrocatalysts to improve the sluggish reaction kinetics and the undesirable selectivity towards NH
3
, while simultaneously suppressing the hydrogen evolution reaction (HER), is critical. Herein, we report a CoO–CuO
x
heterostructure catalyst that is prepared by
in situ
growing Cu(OH)
2
nanoarrays on Cu foam (CF), followed by hydrothermal treatment in the presence of a Co salt. Multiple characterizations revealed that a well-defined heterostructure with a distinct interface is formed between the CoO and CuO
x
phases. In the NtrRR test, the CoO–CuO
x
/CF catalyst displayed a high NH
3
selectivity of 94.29%, an NH
3
faradaic efficiency (FE
NH
3
) of 92.15%, and a high NH
3
yield rate of 0.510 mmol h
−1
cm
−2
. Also, the heterostructure catalyst had remarkable catalytic stability, evidenced by the negligible FE
NH
3
decay after four consecutive cycling tests. This excellent catalytic performance is attributed to the fact that the interfaces in the CuO
x
and CoO heterostructure can facilitate the electron transfer, hence improving the reaction kinetics. This study offers a generic strategy for preparing efficient and durable electrocatalysts toward the NtrRR and other multiple electron/proton-involved electrocatalytic reactions. |
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ISSN: | 2398-4902 2398-4902 |
DOI: | 10.1039/D3SE01024D |